Author manuscript, published in "Progress in Energy and Combustion Science 39 (2013) 340-382" DOI : 10.1016/j.pecs.2013.03.

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Combustion chemical kinetics of biodiesel and related compounds (methyl and ethyl esters): Experiments and modeling Advances and future refinements

Lucie Coniglio*, Hayet Bennadji, Pierre Alexandre Glaude, Olivier Herbinet, Francis Billaud
Universit de Lorraine, cole Nationale Suprieure des Industries Chimiques de Nancy, Laboratoire Ractions et Gnie des Procds, UMR CNRS 7274, 1 rue Grandville BP 20451, 54001 Nancy Cedex, France

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Abstract The motivation for and challenges in reducing the world's dependence on crude oil while simultaneously improving engine performance through better fuel efficiency and reduced exhaust emissions have led to the emergence of new fuels and combustion devices. Over the past ten years, considerable effort has gone into understanding combustion phenomena in relation to emerging fuel streams entering the market. The present article focuses specifically on one typical emerging transportation fuel dedicated to the diesel engine, biodiesel, with an emphasis on ethyl esters because of recently renewed interest in its use as a completely green biofuel. Based on a review of the research developments over the past ten years in advanced experimental and kinetic modeling related to the oxidation of biodiesel and related components, the main gaps in the field are highlighted to facilitate the convergence toward clean and efficient combustion in diesel engines. After briefly outlining the synergy between feedstocks conversion process biodiesel combustion, the combustion kinetics of methyl and ethyl biodiesels are reviewed with emphasis on two complementary aspects: mechanism generation based on a detailed chemical kinetic approach that leads to predictive combustion models and experimental combustion devices that generate the data required during the development and validation of the predictive models. Keywords: Methyl and ethyl biodiesels; Combustion; Diesel engine; Performance and emission; Chemical kinetics of oxidation; Experiments and modeling

*Lucie Coniglio Adress: Universit de Lorraine, cole Nationale Suprieure des Industries Chimiques de Nancy, Laboratoire Ractions et Gnie des Procds, UMR CNRS 7274, 1 rue Grandville BP 20451, 54001 Nancy Cedex, France Tel.: +33 383 175 025; fax: +33 383 322 975. E-mail: lucie.coniglio@univ-lorraine.fr

1. Introduction Energy demand around the world is continuously increasing, including for petroleum-based energy. Petroleum is the single largest energy resource that has been consumed by the world's population, exceeding natural gas, coal, nuclear energy and renewable materials. According to the International Energy Outlook of 2011, which was published by the U.S. Energy Information Administration [2], the world use of liquid fuels will increase from 85.7 million barrels per day in 2008 to 112.2 million barrels per day in 2035. In addition, the transport sector will account for 82% of the total increase in liquid fuel use, with the remaining growth attributed to the industrial sector [2]. Because of the progressive depletion of oil resources in combination with increasing energy consumption and the negative environmental impact of fossil fuel use, there has been a shift toward alternative sources of energy that are renewable, sustainable, efficient, cost-effective and generate reduced emissions [3] and [4]. Biofuels, especially bioethanol and biodiesel, are among the most viable liquid transportation fuels for the foreseeable future and can contribute significantly to sustainable development in terms of socioeconomic and environmental concerns. Liquid biofuels are manufactured from biomass that is mainly derived from agriculture resources (sugar- or grain-based for bioethanols and oilseed-based for biodiesels) [5]. Thus, this natural resource is more evenly distributed geographically than fossil fuels, which provides developed and developing nations with energy supply independence and security, local populations with employment opportunities and rural communities with modern energy [4] and [6]. In addition, biofuels can be used in blends with conventional fossil fuels with no or very little engine modification. Biodiesel is blended with petrodiesel (petroleum diesel, also called fossil diesel) for use in compression-ignition engines, whereas bioethanol is blended with gasoline for use in spark-ignition engines. Regarding environmental concerns, the use of biomass-based energy contributes to a significant reduction in greenhouse gas (GHG) emissions. Biodiesel and bioethanol (when not produced from corn) are considered carbon-neutral fuels because of the equal balance between the carbon dioxide (CO2) released during combustion and that absorbed during the photosynthesis of the raw material used to manufacture the fuels [7]. Furthermore, both biofuels are aromatic-free and lead to a 90% reduction in cancer risk [8]. Biodiesel (bio from life in Greek and diesel from Dr. Rudolf Diesel, German engineer, who invented the diesel engine which is able to run on a host of fuels including coal dust suspended in water, heavy mineral oil, and vegetable oils) is typically produced through the conversion of biolipids with methanol, yielding fatty acid methyl esters (FAME) as biodiesel and glycerol as a by-product. Although methanol has been preferred to bioethanol in industrial applications because of its lower cost [9], biodiesel is 100% renewable only when the alcohol used in the conversion process is also renewable (such as bioethanol); this proportion is reduced to approximately 90 wt% when a fossil alcohol, such as methanol, is used [10]. Furthermore, bioethanol is less toxic, less corrosive and less volatile than methanol, providing thus a safer work environment. In addition, bioethanol is already produced in large quantities in some countries, where it is recommended as transportation fuel [11]. Thus, using bioethanol to produce biodiesel in the form of fatty acid ethyl esters (FAEE) would further enhance the sustainability of new biofuels. In the future, biomethanol (i.e. renewable methanol) could be produced from biomass, either by fermentation or thermal conversion, but the last process being the most promising has to be optimized to become economically viable [12]. For the time being, biodiesel is often assimilated to FAME; however, discussions are underway to include FAEE in its definition [13]. In addition, industrial-scale biodiesel and bioethanol production primarily uses edible agricultural products (rapeseed and soybean crops for biodiesel and sugarcane, wheat, and corn crops for bioethanol). This feature represents a significant weakness in terms of the sustainability of this class of so-called first-generation (1G) biofuels. The limitation of agricultural biomass resources has induced negative outcomes in several ways: socioeconomically due to competition with food crops 2

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and environmentally due to deforestation (leading to a biodiversity reduction) and a shift of pollution (with CO2 consumption by plant photosynthesis compensated by water, air and soil pollution during production and conversion of the resources into biofuels) [14,15]. To this end, alternative feedstocks that do not compete with food crops have been investigated [4,16-18]. Forest and agricultural residues (molasses, grape marcs, or even lignocellulosic residues from the palm oil industry) have been used successfully to produce bioethanol [19,20]. Biolipids have been derived from various resources for the production of biodiesel, including non-edible oils from readily available and sustainable plant biomass, such as Jatropha, Karanja, Mahua or Neem [21-23], and waste cooking oil and animal fats [24-27] or microalgae [28,29]. Such raw materials with adequate conversion processes, which generate so-called second-generation (2G) and third-generation biofuels (3G, for microalgae), have the significant benefits of decreasing GHG emissions and the total production cost (7095% of the reductions are due to the raw material cost in biodiesel production) [30,31]. Furthermore, the diversification of biomass-derived feedstocks and conversion technologies represents a potential mainstay for the long-term security of the supply of sustainable biofuels [32]. The evolution toward alternative transportation fuels necessitates a reevaluation of the adequacy of current engines in terms of performance and emission requirements. Within this context, the United States Department of Energy (DOE) identified an overarching challenge for the 21st century in the field of emerging fuels and engine technologies [33]: The development of a validated, predictive, multi-scale, combustion modeling capability to optimize the design and operation of evolving fuels in advanced engines for transportation applications. Kinetic models with previously established robustness (based on both experiment and theory) built to accurately predict the properties and combustion behavior of virtually any fuel will allow the efficient evaluation of fuel-engine systems through simulation. These advances will permit fuel formulation to be properly defined for a given engine technology (by assessing the influence of additives or new functional groups on fuel performance and emission) and the development of fuel-flexible engine designs with the objective of minimizing emissions while optimizing efficiency [33]. Therefore, a state-of-the-art review of the kinetics of biodiesel combustion was necessary to highlight recent advances, remaining difficulties and future progress. Few review papers have been published on this subject. Kohse-Hinghaus et al. [34] focused on various biofuel combustion chemistries from bioethanol to biodiesel, with particular attention to the analysis of the species composition of laminar premixed flames by molecular beam mass spectrometry and the development of appropriate combustion models. Later, Lai et al. [35] conducted a complementary study that focused on biodiesel fuels with a thorough and critical synthesis of the advances in chemical kinetic modeling related to biodiesel combustion. The present review is specifically concerned with biodiesel fuels and aims to expand on the two aforementioned works by highlighting (i) the experimental aspects of the combustion kinetics that were essential in the development of theory and successful modeling; (ii) FAEE studies, which are much less numerous than FAME studies, and (iii) the pyrolysis of the two classes of esters (FAME and FAEE), as this pure thermal process is an integral part of the combustion kinetics at high temperatures. Furthermore, important studies that provide key research results and conclusions in relation with combustion of biodiesel fuels and that were published after the reviews by Kohse-Hinghaus et al. [34] and Lai et al. [35] will be covered to review the most recent advances. Before addressing the core subject of the manuscript that is the biodiesel combustion kinetics with the outstanding issues and future objectives, the synergy between feedstocks conversion process biodiesel combustion will be briefly outlined. The whole of this information will provide the requisite background for our conclusions regarding the necessary development of fuel-flexible engine technologies and feedstock-flexible conversion processes, and even fuel-flexible production processes, to induce resource diversification and provide a wide range of new fuels. Furthermore, the discussion regarding biodiesel combustion kinetics has been structured to reflect the timeline of the most significant advances to highlight the

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researchers' methodology. The authors have done their best to produce a satisfactory compromise between being concise and detail. 2. Synergy between feedstocks conversion process biodiesel combustion To optimize the selection of next-generation alternative fuels, a wise approach is to consider the synergy existing between feedstocks, conversion process, and biodiesel combustion (the latter requiring a fine knowledge of combustion chemical kinetics in order to formulate a fuel that will lead to cleaner emissions and better engine performance) [36-38]. Indeed, the combustion behavior of a fuel is significantly influenced by its formulation (molecular structures and proportions of the components) which in turn, and particularly in case of biodiesel, is significantly influenced by the feedstocks and conversion process selected to produce it. Hence, all these aspects should be considered simultaneously to isolate a sustainable alternative fuel leading to cleaner emissions and higher performance, not only during combustion but also during production. Also, this global approach should help the use of computational tools integrating kinetic and thermodynamic models in order to orientate reliably the selected feedstocks and conversion process toward the production of a fuel with specific combustion properties (and this, while meeting the sustainability criteria along the entire chain).

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The main features of the chain feedstocks conversion process biodiesel combustion are shortly outlined in the following by focusing on the impacts of resource diversification (biolipids and alcohol). An exhaustive overview of the fundamental and technical aspects at the different stages of the chain can be found in various articles and literature reviews: for the transesterification reaction [12,16,39-74], biodiesel production [4,12,17,18,36-38,42,69,70,77-97], biodiesel properties [5,8,3638,56,98-106], and diesel engine performance and emissions of biodiesel fuel [8,10,36,37,101,107139] (these citations are not exhaustive lists). 2.1. From resources to biodiesel products through transesterification Neat vegetable oils (or any lipid resources) are unsuitable as fuel for modern diesel engines [5]. Poor engine performance and emission characteristics, including engine failure, have been observed even when lipid resources are blended with petrodiesel [107,108]. One method of overcoming these issues is to chemically transform the lipid resources to bring their combustion-related properties closer to those of petrodiesel. By reducing viscosity of the lipid resources significantly, transesterification has long been the preferred method for their chemical conversion and is currently used for generating the biofuel distributed in the market for diesel engines. As depicted by Fig. 1a, transesterification (or alcoholysis) is the reaction of triglycerides (the major components of lipid resources) with an alcohol (methanol or, by extension, ethanol) to form biodiesel (FAME or, by extension, FAEE) and glycerol (by-product). Biodiesel and glycerol are not miscible, and the latter is removed from the reaction medium by decantation. Globally, the stoichiometry for the reaction is 3:1 alcohols to triglycerides (TG), which forms 3 mol of esters (FAME or FAEE) and 1 mol of glycerol. However, a higher alcohol-to-triglyceride molar ratio is used in practice because of the reversibility of the reaction, while an alkali or acid catalyst is usually employed to increase the reaction rate and yield. Furthermore, the overall chemical equation is the result of three consecutive and reversible reactions that lead to the intermediate products of diglycerides (DG) and monoglycerides (MG), as shown in Fig. 1b. As glycerides (TG, DG, and MG) usually contain different aliphatic chains (R1R3), the biodiesel product is a mixture of FAME (or FAEE) with various chain lengths and numbers of double bonds (CH=CH). Table 1 presents, for certain vegetable oils and fats, the average composition of fatty acids corresponding to the fragments RxCOOH with x = 1, 2 or 3 of the triglycerides (Fig. 1a). Normally linked to the glycerol backbone under the triglyceride form, these fragments should be differentiated from free fatty acids 4

(FFA) that may be naturally encountered in the lipid resources (with concentrations below 0.05 wt% in the refined edible oils). As the data in Table 1 show, the major fatty acids in vegetable oils are the saturated fatty acids palmitic (C16:0) and stearic (C18:0) as well as the unsaturated fatty acids oleic (C18:1), linoleic (C18:2), and linolenic (C18:3) [5,56]. Animal fats (including fish oils) contain longer fatty acids (up to 22 carbon atoms) with higher degree of unsaturation (up to 6 double bonds). Thus, the lipidic resources used as raw materials determine the FAME (or FAEE) composition of the biodiesel product.

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Figure 1. Transesterification reaction of triglycerides. (a) Overall chemical equation illustrated for methanolysis yielding FAME (biodiesel) and glycerol (R1, R2, R3 are identical or different aliphatic main chains with zero to three unsaturated bond(s): CH3(CH2)m(CH2CH=CH)n(CH2)k with (m + k) = 12, 14, 16, 18 or 20, and n = 0, 1, 2 or 3 (6 for fish oils) [55]). (b) Alcoholysis of triglycerides as a sequence of three consecutive and reversible reactions. Alkaline catalysis can be used until the free fatty acid (FFA) content in the triglyceride stock is less than 1 wt% [24]. For triglyceride stocks with up to 5 wt% FFA, acidic catalysts have to be selected [42]. Processes based on homogeneous catalysis (mainly alkali catalysis) are the most widely used for industrial biodiesel production [43,44]. Other alternatives based on heterogeneous catalysis were proposed in order to avoid catalyst losses and important water consumptions when removing the catalyst from biodiesel by wet-washing [48-54]. Another alternative, recently recommended at the laboratory scale to replace efficiently the wet-washing step of biodiesel, is a treatment with an adsorbent which can be removed by filtration (such as Magnesol or rice husk ash, a natural by-product of rice processing) [69,79]. Regardless of the method used, the replacement of methanol by ethanol as feedstock causes some issues at key stages of the process: longer reaction times; the formation of more stable emulsions (when they occur), which makes the separation and purification of biodiesel and glycerol more tedious; and a greater solubility of ethanol and glycerol in the ethyl ester rich phase [62-67]. This latter point can be however countered by either evaporating the excess ethanol or adding cold glycerol [65,66]. Nevertheless, a much more critical issue than the aforementioned ones is the deactivation of the catalyst by the presence of water in the non-conventional feedstocks, such as crude bioethanol and 2G or 3G biolipids (non-edible oils, waste cooking oils, or microalgae). Thus, the raw materials for catalyzed transesterification reactions should have a water content below 0.06 wt% [4,16,36,39]. Emerging non-catalytic alcoholysis methods based on supercritical fluids (the alcohol with eventually a co-solvent like CO2) allow to avoid these problems while offering other significant advantages: short reaction times; high-grade products (99.8% biodiesel and 96.4% glycerol), which renders glycerol more valuable on the market and further lowers the manufacturing costs [94], [95], [96] and [97]; a flexibility in terms of feedstocks with high concentrations of FFA and water (up to 36 and 30 wt%, respectively) [37,55,71-76,84-86,91,92]. The main drawback of the supercritical (SC) 5

process is its high energy demand, which could be countered by the addition of CO2 (co-solvent) [61], [87], [88] and [93], with the integration of a heat-exchanger network [89] or the use of both biodiesel and heat power (cogeneration) [90]. Additionally, a new conceptual design of in situ generation of biodiesel fuel via SC-TG transesterification coupled with SC fuel injection and combustion was very recently proposed [37]. Table 1. Average fatty acid compositions of some vegetable oils and fats [5] and [56].a
Vegetable oil Palmitic acid C16:0 Palmitoleic acid C16:1(7) 0 0 0 0.1 0.3 0.3 0.3 0.1 0 0 0 Stearic acid C18:0 0.9 2.0 1.9 2.9 2.5 4.4 4.1 19.3 6.8 19.3 5.6 Oleic acid C18:1(9) 13.0 62.2 13.6 17.7 18.9 40.5 23.2 44.4 41.7 55.5 71.3 Linoleic acid C18:2(6) 57.4 22.0 77.2 72.9 18.1 10.1 54.2 2.9 35.6 9.0 15.0 Linolenic acid C18:3(3) 0 10.0 0 0 55.1 0.2 6.3 0.9 0.1 0 0 Others (C14b or c C20 ) 0 0 0 0 0 b 1.1 0 b 2.9 c 2.0 0 2.3c

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Cottonseed 28.7 Rapeseed 3.8 Safflower 7.3 seed Sunflower 6.4 seed Linseed 5.1 Palm 43.4 Soybean 11.9 Tallow 29.5 Jatropha 13.8 Neem 17.6 Karanja 5.8 d Extended molecular structures

In Cxx:n(y), xx: number of carbon atoms; n: number of double bonds; y: position of the first double bond on the aliphatic main chain, starting from the extremity CH3. b Myristic acid. c Arachidic acid. d When R = H, CH3 or C2H5, molecules are respectively FFA, FAME or FAEE.

In light of recent scientific and technological advances [37,55,71-75,89-93], biodiesel produced from 2G or 3G biolipids and crude bioethanol by the non-catalytic supercritical process integrating both CO2 as co-solvent and cogeneration seems a promising approach for the sustainable production of renewable energy. One particular significant feature of this alternative is that it takes advantage of the long-aliphatic chains available in the TG, which is contrary to other biofuel alternatives, such as FischerTropsch (FT) diesel derived from a conversion process that cleaves the molecules available in wood materials into much smaller molecules (synthesis gas) before re-building them through another catalytic process into hydrocarbons with long-aliphatic chains. Another alternative, which is somewhere between biodiesel and FT-diesel, is the hydrodeoxygenation of lipid raw materials that

leads to long-chain hydrocarbons, known as renewable diesel. Knothe [38] concluded in his review that biodiesel and renewable diesel complement each other rather than compete. Nevertheless, the process production for the renewable diesel requires the use of a catalyst, which may be somewhat restrictive in terms of the nature of the lipid feedstock (particularly regarding water content). 2.2. Key physical and thermal properties of biodiesels as fuels quality specifications The properties of the produced biodiesel must adhere with specifications such as the American ASTM D6751 standard or the European EN 14214 standard. As illustrated in Table 2, which presents the ranges of the most significant quality specifications for biodiesel and petrodiesel, the fuels are very similar in some ways and quite different in others. This highlights why biodiesel is a strong candidate for replacing petrodiesel as well as the advantages and drawbacks of each fuel type. General features related to the physical and thermal properties are summarized below [5,8,33,36,100-102], whereas the other properties related to engine emission and performance characteristics will be discussed further in the dedicated section. Table 2. Some quality specifications related to biodiesel and petrodiesel comparison with vegetable oils [5,98].
Specifications
a

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Units kg/m cSt (mm2/s) C

3

Vegetable oils [5] 902946 2254 150293 3549 3.9 to 31 40 to 6.7 3950 n/a

Biodiesel ASTM D6751 EN 14214 880 1.96.0 Min. 100170 Min. 47 3 to 12 15 to 16 Max. 0.05 % (v/v) Max. 0.50 860900 3.55.0 >120 Min. 51 35 Max. 500 (mg/kg) Max. 0.50 96.5% (m/m) 0.25 10 (mg/kg)

C C MJ/kg % (v/v) or(mg/kg) Acid number mg KOH/g n/a Ester content % (m/m) or % n/a (v/v) Total glycerin content % (m/m) n/a Max. 0.24 Sulfur content % (m/m) or n/a Max. 0.05% 0.05% (mg/kg) (m/m) (m/m) a Definition of most specific properties are given here, with the exception of cetane number and lower heating value which will be explained in section related to diesel engine emissions and performance of biodiesel fuels. Flash point (lowest temperature corrected to a pressure of 101.3 kPa at which application of an ignition source causes the vapors of a specimen to ignite under the specified conditions of test, i.e. measure of residual alcohol in the B100). Cloud point (temperature at which a cloud of wax crystals first appears in a liquid when it is cooled down under conditions prescribed by the specific test method). Pour point (lowest temperature at which a liquid will pour or flow under conditions prescribed by the specific test method). Lower heating value (enthalpy of combustion by considering that water is in the vapor state in the exhaust product). Acid number (quantity of base, expressed as milligrams of potassium hydroxide per gram of sample, required to titrate a sample to a specified end point). Total glycerin content (sum of the free glycerin and bonded glycerin as glycerides). n/a: no information available in the reviewed literature.

Density (15 C) Kinematic viscosity (40 C) Flash point Cetane number Cloud point Pour point Lower heating value Water content

Petrodiesel ASTM EN 590 D975 850 820845 2.6 2.04.5 6080 4055 20 35 4246 0.05 % (v/v) 0.062 >55 Min. 51 20 to 5 Max. 200 (mg/kg) Max. 5% (v/v) 10 (mg/kg)

The most obvious advantages of biodiesel versus petrodiesel are the following: Biodiesel is sulfur-free (producing full compatibility with catalytic post-treatment systems). When blended with petrodiesel, biodiesel enhances the ignition quality (through a higher cetane number) and lubricity characteristics of petrodiesel (which is mainly a result of the polarity of the oxygenated biodiesel components, not only the FAME but also more specifically the minor components, such as the FFA, MG, and glycerol). Biodiesel has a higher flash point (leading to safer handling, transport, and storage).

Regarding the main disadvantages associated with biodiesel versus petrodiesel, the following should be mentioned: Biodiesel has poorer low-temperature properties such as the cloud point and pour point (which can create problems in cold weather by plugging fuel filters). In addition to density, biodiesel also has a higher viscosity (which generally leads to poorer atomization of the fuel spray, affects the accuracy of the operation of fuel injectors, and inhibits the nebulization of fuel in the ignition chamber). This drawback is not obviated despite the transesterification process that reduces significantly the viscosity of the departure lipid resources (Table 2). Biodiesel is inherently less stable to air and high-temperature exposure (particularly because of the possible occurrence of polyunsaturated FAME among biodiesel components), which requires the addition of small amounts of stabilizers for long-term storage. Impurities, such as unreacted FFA or alcohol as well as glycerol or leftover catalyst from the production process, can accelerate engine wear or corrosion and the production of acrolein, which is a photochemical smog precursor (however, those same polar components also enhance the lubrication characteristics of biodiesel). All the aforementioned issues highly depend on the fatty acid profile.

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Thus, it becomes clear that the ideal biodiesel should be a compromise of well-balanced components that satisfies the quality specifications. Ramos et al. [30] presented a triangular graph (Fig. 2) that describes the optimum concentrations of saturated, monounsaturated, and polyunsaturated FAME, leading to a biodiesel that satisfies the limits imposed by EN 14214, a standard for critical parameters such as cetane number, iodine value (measure of the total unsaturation within the given biodiesel) and CFPP (cold-filter plugging point determined using a lowtemperature filterability test). This area was characterized by a high concentration of monounsaturated FAME (such as oleic acid methyl ester, C18:1(9)) encountered in oleic sunflower or rapeseed oil biodiesel.

Figure 2. Biodiesel by saturated, monounsaturated, polyunsaturated FAME and areas verifying the limits imposed by European standard EN 14214 for cetane number, iodine value, and CFPP; yellow (right): good cetane number and iodine value; blue (left): good CFPP; green (intersection): biodiesel that satisfies EN 14214 standard [30].(For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.) 2.3. Biodiesel combustion in diesel engines Insight of key macroscopic features of fuel combustion as well as analysis of the diesel engine performance and emissions are necessary to understand and then predict the phenomena that

govern them at the microscopic scale, such as fuel combustion kinetics. This aspect is addressed in this section by focusing on biodiesel fuels. 2.3.1. Key macroscopic features of fuel combustion 2.3.1.1. Heat release rate An important combustion parameter linked to the chemical reaction is the heat release rate (HRR), the rate of heat emission just after ignition. Although determined indirectly during combustion in diesel engines, the HRR can provide meaningful information regarding the combustion process. As illustrated in Fig. 3 [103], the HRR history as a function of crank angle degrees may show one or two peaks, depending on the nature of the fuel and combustion conditions. In the event of two peaks, the first peak, designated as the low-temperature heat release (LTHR), corresponds to the first-stage ignition, which is representative of low-temperature oxidation, i.e. cool flame regime. The second peak, designated as the high-temperature heat release (HTHR), corresponds to the second-stage ignition, which is representative of the high-temperature combustion. In one-peak conditions, this peak may correspond to either the LTHR or HTHR phenomena.

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Figure 3. Definition of combustion parameters determined from heat release rate data [103]. ALTHR and AHTHR are the net energy (in J) released during the first and second stage of combustion. 2.3.1.2. Cetane number and ignition delay: molecular structureemissions relationship One of the most important characteristic of a diesel fuel is its ignition delay (the period between the start of injection and the start of combustion). The engine test used to characterize a fuel is the Cetane Number (CN) test, which grades autoignition quality of the diesel fuel. Fuels with a high CN will have short ignition delays (IDs). The primary reference fuels used for CN are cetane (n-hexadecane) with an assigned CN of 100 and 2,2,4,4,6,8,8-heptamethylnonane with an assigned CN of 15. Saturated and unbranched hydrocarbons with long-aliphatic chains have high CN and good ignition ability as a diesel fuel compared to unsaturated or branched molecules [104]. Regarding biodiesel components, two structural effects influence the CN: the skeleton of the aliphatic chain (length and number of double bonds) and the nature of the alcohol moiety (methyl, ethyl, etc.). Knothe et al. [105] determined the CNs of 29 mono-alkyl esters of fatty acids using an Ignition Quality Test. The authors observed that CNs increased with chain length (as hydrocarbons), whereas

increasing the number of double bonds or branching in the aliphatic main chain decreased CNs. Among the investigated fatty acid esters, the lowest and highest CN values were observed for linolenic acid and stearic acid, respectively, with CN increasing in the order linolenic < linoleic < oleic < palmitic < stearic acid. If the effect of the alcohol moiety was less defined, all ethyl esters experienced higher CNs compared to the corresponding methyl esters. In addition, the esters of 2-ethylhexanol, the most CH2-rich alcohol used by the authors, displayed the highest CN of all tested esters. Although engine emissions have been observed to be closely linked to CN and to the molecular structure of the fuel components, the relationship between emissions and CN is complicated by many factors, including the type of engine and the operating conditions [109]. Emissions of nitrogen oxides (NOx) and unburned hydrocarbons decreased with an increasing CN because of a reduction in ID times and amount of premixed fuel burned, which resulted lower average combustion temperatures and advanced combustion [110]. Nevertheless, running a diesel engine with various types of biofuels revealed that a lower CN and a longer ID period (higher level of premixed combustion) may increase the exergetic efficiency [111]. This finding highlights the necessity of further research for a better understanding of the relationship between macroscopic fuel properties, engine emissions and performance characteristics.

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2.3.2. Diesel engine emissions and performance of biodiesels Biodiesel is an oxygenated fuel containing approximately 1015% oxygen by weight, which results in cleaner combustion and improves exhaust emissions. Of all regulated emissions, nitrogen oxides (NOx) and particle matter (PM) are the most critical factors in diesel engine emissions because current technologies are close to the permitted limits, which will be even more stringent in the near future, and because new regulations (Euro 5 and 6) will consider mass- and number-based PM emissions. In addition, while current diesel engine technologies should be able to meet the future limits for regulated emissions (e.g. CO, total hydrocarbons), this is not guaranteed for some nonregulated specific emissions, such as polycyclic aromatic hydrocarbons (PAH) and carbonyl compounds, which raises concerns because of their hazards to humans and the environment. Assessment of biodiesel emissions and their impact is required before expanding the availability of biodiesels in the fuel market. The trends emerging from the reviewed literature detailed below regarding engine performance and emissions of biodiesel (FAME and FAEE) and petrodiesel are summarized in Table 3. If a wide range of diesel engines was tested, few tests were conducted using actual vehicles [112-116]. 2.3.2.1. FAME-biodiesel versus petrodiesel Recent reviews summarized scientific work on combustion performance and emission of biodiesel fuels in diesel engines [33,117], compared to conventional petrodiesel fuels [10] or focused on the separation and purification technologies that lead to high-quality biodiesel and its effects on diesel engines [36]. Most researchers have reported that the diesel engine combustion of biodiesel fuels (irrespective of feedstock) results in a decrease in particulate matter (PM), unburned hydrocarbons (UHC), sulfur oxides (SOx), volatile organic compounds (VOCs), and carbon monoxide (CO) emissions compared with petrodiesel fuel [5,8,10,107,117-120]. An increase in nitrogen oxide (NOx) emissions was often reported [8,10,17,117,120-121], although no consensus has been determined. Some studies reported an NOx increase [119,122], while others did not find significant differences between petrodiesel and biodiesel fuels [123], and yet others observed decreases when using biodiesel [114,124]. Some causes of this disagreement are the large variety of engine technologies, operating conditions, biodiesel fuels, and measurement techniques used [10,117]. It is generally accepted that NOx emissions are influenced by coupled physical and 10

chemical phenomena [35,121,125]. A mitigation of the effect of biodiesel on NOx emissions could be achieved by delaying injection (which is slightly advanced with biodiesel because of its physical properties) in combination with increasing exhaust-gas recirculation [10,126], or by increasing the spray-cone angle combined with an advanced start of injection [127] or even by the use of indirect injection combustion systems (ICS) [128]. A reduction of the aromatic content and the use of cetane improvers were also proposed [10] and [125]. It is generally agreed that the formation of NOx during combustion is mainly controlled by the ignition delay of the fuel and the relative amounts of heat released during the premixed combustion phase and diffusion-controlled combustion phase [121]. A longer ignition delay strongly increases NOx formation [129]. According to the correlation between ignition characteristics and molecular structures of fuel components, increasing the fatty acid chain length, saturation, and chain length of the alcohol moiety are expected to decrease the ID, and therefore NOx formation [105,129,130]. Fortunately, sophisticated after-treatment systems required to achieve the 2010 diesel engine emission standards do not appear to be significantly affected by the use of biodiesel [125]. Table 3. Average trends from the reviewed literature regarding emissions and engine performance when using biodiesel from various raw materials. The comparative fuel behavior is described qualitatively via patterns: + when better, when worse, when equivalent, +/ when dependent of the engine operating conditions, and n/a when no information is available on the basis of the reviewed literature; the reason of this notation is also given ( for increase and for decrease, corresponding implicitly to ). Dependence on the nature of the lipid raw materials is specified in parenthesis by yes, no, or n/a (no information available in the reviewed literature).
Emissions Regulated NOx PM THC (or UHC) CO Non-regulated PSD Large particles Small particles Ultrafine particles Carbonyl compounds PAH SOx CO2 Performance Effective power (full road) BSFC BTE FAME versus Petrodiesel FAEE versus petrodiesel FAME versus FAEE (dependence in terms of the lipid raw materials) or (yes) + (no) + (no) + (no) + (yes) + or (yes) + or (yes) or (yes) or (yes) +/ (yes) + (no) + (no) (n/a) (no) +/ or (yes) +/ (yes) +/ (no) + (no) + (no) n/a n/a n/a n/a n/a n/a n/a +/ (no) +/ (n/a) +/ (yes) (yes) (no) +/ (no) (no) (no) n/a n/a n/a n/a n/a n/a n/a + (no) + or (n/a) + or (n/a) + or (n/a)

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Three other classes of harmful emissions remain subject to controversy: (i) the proportion of fine particles (less than 10 m) emitted; (ii) polycyclic aromatic hydrocarbons (PAH); and (iii) carbonyl compounds, such as aldehydes and ketones, which are carcinogenic and mutagenic for the lighter ones and potential ozone-precursors. Most studies have reported decreases in the mean diameter of the particle size distributions (PSD) with biodiesel, attributed to a sharp decrease in the number of large particles by some authors, while others observed an increase in the number of smallest particles [131-133]. While reduction in soot emissions has been virtually always obtained when biodiesel was added to diesel fuel [133] and [134], no conclusive trend was observed regarding the emission of PAH: while RME and SME produced similarly low emissions of PAH compared to petroleum fuels, the opposite effect was observed with neat rapeseed oil [108]. However, Karavalakis et al. [113] observed that the addition of biodiesel led to an important increase in lowmolecular-weight PAH (phenanthrene and anthracene), and to an increase or reduction of heavier

11

PAH species, depending on the nature of FAME used. This lack of knowledge is even greater regarding the emissions of carbonyl compounds, such as aldehydes and ketones, for which very few studies have been performed. Systematic increases in carbonyl emissions were detected by He et al. [135] with an engine fueled with SME compared to petrodiesel. However, Fontaras et al. [115] observed that low-concentration biodiesel blends had a minor impact on carbonyl compound emissions. Nevertheless, this impact was determined to be dependent on the nature of the biodiesel: some such as RME resulted in significant increases, while others such as palm oil FAME led to decreases. Hence, similar to the NOx issue, all harmful emissions are interdependent of the physical and chemical combustion parameters. Therefore, the impact of each should be investigated separately within a referential well defined framework allowing meaningful comparisons [10,115,117,135]. Regarding engine performance, conventional engines can be operated with biodiesel without major modification. In addition, blended or neat biodiesel does not cause any loss of power output unless maximum power is demanded and generally leads to a similar thermal efficiency as petrodiesel fuel [5,8,10,117,119]. Nevertheless, an increase in fuel consumption because of the lower heating value of biodiesel compared to petrodiesel (Table 2) was reported [10]. Among the various tests of biodiesel blends, B20 (20%vol. FAME with 80%vol. petrodiesel) provided the maximum improvement in terms of emissions and performance and was recommended for long-term engine operation [8]. 2.3.2.2. FAEE biodiesel versus petrodiesel and analysis in terms of various biolipid raw materials Far fewer studies detail the effect of ethanol-derived biodiesel (FAEE) on diesel engine performance and emissions than the effect of methanol-derived biodiesel (FAME). Peterson et al. [112] tested exhaust emissions from a diesel vehicle fueled with neat rapeseed oil ethyl esters (REE). The authors reported that UHC, CO and NOx emissions decreased by 55.6%, 50.6%, and 11.8%, respectively, compared with petrodiesel fuel. An increase in CO2 (1.1%) and PM (10.3%) was observed. Nevertheless, a blend of 20% REE and 80% petrodiesel led to a decrease in PM emission of 5.7% compared to neat petrodiesel fuel. Nearly the same trends were observed by Makareviciene and Janulis [136] with a direct injection 4 cylinders diesel Audi 80 engine fueled with petrodiesel, blends of biodiesel/petrodiesel (2575%vol.) or neat biodiesel. Substituting petrodiesel with neat REE, led to a reduction in CO and UHC emissions and smoke density of 7.2, 53.0, and 72.6%, respectively, and a slight increase in NOx emissions (8.3%). Nevertheless, the reverse trend was obtained for NOx emissions with the B25B50 blends in REE/petrodiesel. Al-Widyan et al. [137] studied the use of different blends of waste vegetable oil ethyl esters (WVOEE) with petrodiesel in a single-cylinder DI diesel engine. The blends produced fewer CO and UHC emissions than did neat petrodiesel. The authors also indicated that the blends burned more efficiently with less fuel consumption and higher power output. Overall, the best engine performances were obtained with 100% WVOEE and 75:25 WVOEE/petrodiesel blends, while the 50:50 blend produced the lowest emissions. Puhana et al. [138] extended the latter work by separately testing petrodiesel and non-edible Mahua oil ethyl esters (MOEE). The authors reported that the fuel consumption for MOEE was higher than for petrodiesel fuel due to the combined effect of a low heating value and high density of MOEE. The emissions of CO, UHC, and NOx, were reduced by approximately 58, 63, and 12%, respectively, in MOEE compared to petrodiesel fuel. 2.3.2.3. FAME versus FAEE as biodiesel and analysis in terms of various biolipid raw materials In addition to the evaluation of REE performance versus petrodiesel, Makareviciene and Janulis [136] also compared the environmental effect of REE with RME. Results indicated that REE had better environmental effects than RME in terms of CO, NOx, and smoke emissions. Moreover, REE was 12

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more biodegradable in an aqueous environment than RME. Lapuerta et al. [123] studied the performance characteristics and emissions of waste cooking oil methyl and ethyl esters (WCOME and WCOEE, respectively) in a 4 cylinder, turbocharged, direct injection Nissan diesel engine. The biodiesels were tested neat and blended at 30% and 70%vol. with a low-sulfur petrodiesel fuel. Exhaust analysis showed that WCOEE produced fewer NOx emissions than WCOME, explained by a lower premixed combustion of WCOEE. Total hydrocarbon emissions were also impacted by the type of alcohol used in the biodiesel production: emissions were increased with more volatile alcohol, meaning that WCOME was less favorable than WCOEE. Nevertheless, a slightly higher reduction in opacity and PM emissions was observed with WCOME (consistent with a higher oxygen content). Baiju et al. [122] performed a comparative evaluation of compression-ignition engine characteristics using methyl and ethyl esters of Karanja oil (KOME and KOEE, respectively), a non-edible oil that can be extensively grown in the wastelands of India. Compared with KOME, KOEE showed slightly higher viscosity and reduced cold-flow properties as well as a higher flash point. These observations, consistent with previous studies [106,139], make FAEE a safer fuel for storage and transport than FAME. Regarding engine performance and exhaust emissions, KOME yielded slightly better characteristics than KOEE in terms of power output, brake thermal efficiency (BTE), and fuel consumption. A slightly cleaner behavior for KOME was observed; however, these last results are in disagreement with other studies [123,136] regarding CO and NOx emissions.

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In summary, although biodiesel engine performance has been determined to be slightly inferior but similar overall to that of petrodiesel, biodiesel contributes to reduce pollutant emissions. Nevertheless, this argument must be confirmed, particularly for the non-regulated emissions and performance of FAEE versus FAME, with consideration of the lipid raw material origins. Modeling studies reinforced with suitable experimental information would provide a better understanding and more accurate prediction of engine performance and emissions for a given biodiesel fuel. 3. Biodiesel combustion kinetics The oxidation kinetics of hydrocarbons has been the subject of numerous studies, as presented in recent literature reviews related to this subject [140,141]. However, fewer kinetic studies related to the oxidation of biodiesel have been performed at the experimental and modeling levels. The main reason for this lack of information is the molecular structure of actual biodiesel components (saturated and unsaturated fatty acid methyl or ethyl esters), which involves large aliphatic main chains of 1420 carbon atoms with CH2CH=CH and ester groups (Fig. 1, Table 1); this complexity in the molecular structure of reactants poses a significant challenge to modeling and experimental kinetic studies. Therefore, this part of the review focuses on oxidation modeling of biodiesel (surrogates and neat fuel) using detailed chemical kinetic mechanisms and the experiments that are a prerequisite for the development and validation of the corresponding models. These models are generated using theoretical-based approaches that account for thermodynamic and kinetic phenomena. 3.1. Main features of model development and validation 3.1.1. Detailed chemical kinetic models and their foundation Models based on detailed chemical kinetic mechanisms can accurately predict hydrocarbon reactivity in the presence of oxygen [140,141]. This success is mainly due to their core methodology, describing at the molecular level the chemical changes occurring during the reactions. This molecular approach has two results. First, most of the proposed mechanisms have been detailed systematically by using similar reaction classes and drawing a well-accepted general kinetic scheme related to the primary oxidation reactions of the fuel molecule and its derived species (molecular and radical species). The 13

slight differences between the reaction classes used by the different research teams are described exhaustively in the Battin-Leclerc literature review [141] for the combustion of alkanes. Second, fuels comprising heavy molecules (with more than 6 carbon atoms) involve complex mechanisms. Therefore, two types of approaches were adopted in the development of mechanisms and derived kinetic models, depending on whether a computer was used or not. Mechanisms (and derived kinetic models), developed without computer assistance, were generally built iteratively by modules, starting with small esters and progressing to larger ones. For example, the research team of LLNL (Lawrence Livermore National Laboratory) developed successively models for methyl decanoate [142], methyl decenoates [143], then methyl stearate and oleate [144], and eventually a mixture representing the main components of soybean and rapeseed methyl esters [145]. The research team of Milan proposed lumped mechanisms (i.e. with globalization of species and/or elementary reactions) based on the same reaction classes for methyl butanoate [146], decanoate [147], and biodiesel fuels [148]. However, software-generated mechanisms did not include previous submechanisms and were usually smaller due to tailoring the required mechanisms to the operating conditions of study. Hence, with EXGAS software (which is primarily intended for hydrocarbons, such as alkanes [149,150] and alkenes [151] and extended to biodiesels and derivatives [152,153], as will be discussed in the following sections), only the significant classes of reactions for the temperature range of the study may be activated using a menu.

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For all mechanisms, the thermodynamic properties were determined using software, i.e. THERM [154] for non-computer-based mechanisms and THERGAS [155] for computer-aided mechanisms. When no thermodynamic properties were available in the literature or stored in the software databank, the thermodynamic properties were automatically computed using the implemented method, usually the Benson method [156] with updated group contribution and bond additivity values. Concerning the kinetic properties, information available in the literature and stored in the software databank was used as a first option. When unavailable, the kinetic properties were usually estimated using correlations based on quantitative structurereactivity relationships or quantum calculations. More precisely, each elementary reaction of the mechanism was written as a reversible reaction, and the reverse rate constant was computed from the corresponding forward rate constant and appropriate equilibrium constant Kc = kforward/kreverse calculated from thermochemical data. Concerning EXGAS software, KINGAS subroutine [157] was devoted to kinetic property calculations. 3.1.2. Model validation: experiments and environment modelling Oxidation experiments were conducted in various physical environments. The equipment used were selected to cover a wide range of reactors with different geometries (shock tube, premixed flames, diffusion flames, continuous jet-stirred reactor, plug-flow reactor, variable pressure-flow reactor, or internal combustion engines) in which experiments could be conducted at a wide range of temperatures, pressures, and biodiesel/oxygen equivalence ratios : < 1 for fuel-lean mixtures and > 1 for fuel-rich mixtures (see nomenclature for definition).1 Most experiments provided speciesdependent and time-dependent information, which is particularly valuable and relevant for model development and validation (with the exception of shock tubes yielding integrated information, such as ignition delay). Therefore, experimental information generated from this large panel of physical environments warranted wide-ranging kinetic modeling. However, while kinetic modeling aims to
1

This definition corresponds to the traditional equivalence ratio, in which the oxygen atoms contained in a fuel molecule are still part of the fuel, functioning as an oxidizer during the oxidation process. Therefore, the concept of the oxygen equivalence ratio, which is considered a more appropriate representation of the mixture stoichiometry for oxygenated fuels than the traditional equivalence ratio, was introduced [1]. The oxygen equivalence ratio is defined as the oxygen content available in the reactant mixture divided by the amount of oxygen required for stoichiometric combustion.

14

account for chemical phenomena, suitable and reliable reactor modeling is required to account for the physical environment. All of these features must be gathered to perform reliable predictions of the fuel behavior during ignition, combustion, and emission in diesel and homogeneous-charge compression-ignition (HCCI) engines. Within this context, CHEMKIN library software [158], which enables the modeling of a wide range of reactors, was the most widely used tool in the scientific community related to kinetics. The standardization of the CHEMKIN input data format for describing the reactions, rate parameters, thermodynamic data, and transport properties of species favored this common use by facilitating the exchange of models between scientists [141]. 3.1.3. Main guidelines of past research and the present review Two major paths were followed in past research related to biodiesel oxidation for the reliable prediction of engine behavior. The first path is devoted to oxidation experiments and kinetic modeling oriented to small methyl and ethyl esters with 14 carbon atoms (C1C4) in their aliphatic main chain. These works provided detailed information on the special features of methyl and ethyl ester group reactivity for future studies. The second path is devoted to generating experimental information by conducting the oxidation of actual biodiesel fuel and components and then comparing the experimental results with the simulation results obtained from the oxidation mechanisms of large n-alkanes. This approach assumes that large n-alkanes and fatty acid methyl or ethyl esters with the same number of carbon atoms in their aliphatic main chain behave similarly during oxidation. Nevertheless, the authors agreed that all alkyl esters with an aliphatic main chain at C1C2 were too small to be considered as potential biodiesel surrogates (i.e. methyl and ethyl formate or acetate [159-163]). The first molecule considered as an acceptable biodiesel surrogate among the small alkyl esters investigated was methyl butanoate with an aliphatic main chain at position C4. Studies that followed however showed that this molecule was not a very suitable surrogate fuel for biodiesel study in general, but rather a model providing insight into kinetics of the methyl ester function. Thus, further research extended the kinetic modeling capabilities to alkyl esters with larger aliphatic main chains for the reliable reproduction of the reactivity of actual biodiesel components, such as early (low-temperature) CO2 production from the ester group and burning similar to petrodiesel. These features are described in more detail in the following sections after the presentation of some additional chemical bases of the combustion process. In the following, alkyl (methyl or ethyl) esters with aliphatic main chains comprised of n carbon atoms will be designated Cn-alkyl esters; thus Cn-methyl (ethyl) esters will designate molecules with n + 1 (n + 2) carbon atoms. The experimental data generated for the oxidation (and occasionally pyrolysis) of alkyl esters selected as biodiesel surrogates are summarized in Table 4 [1,153,164-194], whereas the main features related to the developed chemical kinetic models are presented in Table 5 [142-148,151-155,157,166,167,169-171,174,182,184,188-190,197,201,203,206-216]. Table 4. Summary of the main experimental data generated for oxidation of alkyl esters selected as biodiesel surrogates.
Fuel Equipment (Data type) FR (SP) CFNPF (SP) JSR (SP) OFDF (SP) VPFR (SP) ST (ID) Temperaturea/K Pressure/atm Equivalence ratio (Fuel molar fraction %) 0.351.5 (800 ppm) (5000 ppm + CH4) 1.13 (0.075) (4.7) 0.351.5 () 0.251.5 () Reference

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Methyl Butanoate

500900 8001350 500900 11001670

12.5 1 1 1 12.5 14

[164] [165] [166] [167]

15

JSR (SP) OFDF (SP) JSR (SP) RCM (ID) ST (ID) RCM (ID) RCM (ID) ST (CO2 yields) JSR (SP) ST (ID) ST (ID) ST (ID, concentration time-histories of CO, CO2, CH3, and C2H4) Counterflow flame (Laminar flame speeds and local extinction strain rates) Counterflow flame (extinction strain rates) Flame and bomb (Laminar flame speeds and local extinction strain rates) Flame (SP) OFDF (SP) JSR (SP) JSR (SP) Flame (SP) JSR (SP) RCM (ID) JSR (SP) JSR (SP) OFDF (SP) ST (ID) Variable CR octane rating (HRR versus CAD and exhaust SP) Flame (Counter flow extinction and ignition critical conditions) OFDF (SP) JSR (SP) JSR (SP) Counterflow

8501350 355413 8501400 640949 12501760 9351117 650850 12601653 800850 12502000 10601632 12001800

1 1 1 1040 14 4.719.6 3.919.7 1.41.7 1 7.69.1 1.211.4 1.5

1.0 (0.075) (4.7) 0.375 and 0.75 (0.075) 0.331.0 (1.59 3.13) 0.251.5 (1.0 1.5) 0.30.4 (0.95 1.27) 1.0 () Pyrolysis study (23) 0.51.0 (2) 0.252 (0.51) 0.52.0 (0.64 3.32) Pyrolysis (0.01, 0.05, 0.1)

[168] [169] [170]

[171] [172] [173] [174] [175] [176]

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403b

0.71.6 (in air)

[177]

298/500 353b

1 1.03.0

(0.100.18) 0.71.7 (in air)

[178] [179]

Methyl Crotonate

355413 8501350 8501400 5001100 650850 5501150 8001350 400420 12501550 4002000

0.04 (30 Torr) 1 1 1 0.04 (30 Torr) 10 3.919.7 10 1 1 110 CR range 4.0 13.7 1

Methyl Hexanoate Methyl Heptanoate Methyl Octanoate Methyl Decanoate

1.56 (0.14) (4.7) 1 (0.075) 0.375 and 0.75 (0.075) 1.56 (0.14) 0.5, 1, 1.5 (0.1) 1.0 () 12 (0.001) 0.52 () (1.8%) 0.5, 1, 2 (380 1380 ppm) 0.252

[180] [168] [169] [181] [182] [172] [183] [184] [185] [186,187]

9001600

0.51.5 ()

[188]

400420 5001100 7731123 403

b

1 1.06 1.05 1

(1.8%) 1 (0.0021) Pyrolysis study (0.0218) 0.71.6 (in air)

[189] [153] [190] [177]

16

flame (Laminar flame speeds and local extinction strain rates) Flow Reactor (SP) ST (ID) Methyl Palmitate (MP) (ndecane/MP) Methyl Oleate (MO) (ndecane/MO) Methyl Oleate (neat) Methyl Linoleate Rapeseed Methyl Esters (RME) Palm Methyl Esters RME/kerosene (20/80 mol/mol) Commercial B30 fuel & B30 surrogate fuel (49% n-decane, 21% 1methylnaphtlene, 30% MO in mole) Ethyl Propanoate (EP) with MiBu, PrAc, and iPrAc for comparison EP ST (ID) JSR (SP) JSR (SP) ST (ID) ST (ID) JSR (SP) Tube (SP) Flame (Laminar flame speeds) JSR (SP) JSR (SP)

8731123 6531336 8381381 5001000 5501100 11001400 11001400 8001400 8231073 b 470 7401200 5601030

1.7 1516 1.718.63 1 1 3.57.0 3.57.0 110 1 1 1 6 and 10

Pyrolysis (0.091 0.625) 0.5, 1.0, 1.5 (in air) 0.12 (in air) 1 (0.002) 1 (0.002) 0.62.4 (0.04) 0.62.4 (0.04) 0.25, 0.5, 1, 1.5 (0.05) Pyrolysis (0.07) 0.71.4 (in air) 0.51.5 () 0.251.5 (10,300 ppm of carbon)

[191] [192] [193] [194] [195] [196] [196] [197] [198] [199] [200] [201]

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CFNPF (SP)

(5000 ppm + CH4) 0.251.5 () 0.31 (0.1) 0.30.4 (0.95 1.27) 0.252 (0.417) 0.51.6 (0.013) 06, 1, 2 (1000 ppm) 0.71.4 (in air) 0.25 ()

[165]

ST (ID) JSR (SP) RCM (ID) ST (ID) Laminar PFR JSR (SP) Bomb (Laminar flame speeds) CFR motored engine (exhaust SP)

11401675 7501100 9351117 12502000 5001200 5601160 423b 6501850 (bulk cylinder gas temperature)

14 1 4.719.6 7.69.1 1.031.35 10 110 CR range 4.4315

[167] [202] [171] [174] [203] [204]

Ethyl Butanoate Ethyl Pentanoate

CFR motored 6001650 (bulk CR range 4.43 0.25 () [205] engine (exhaust cylinder gas 10.5 SP) temperature) a Extreme temperature given for OFDF equipment is related to the temperatures of the gases exiting the bottom and top burner ports respectively. b Fresh gas temperature.

EN with: MN, MN2EN, and MN3EN for comparison EHX with MH for comparison

[1]

17

Table 5. Summary of the main features related to the chemical kinetic models proposed for the oxidation of alkyl esters selected as biodiesel surrogates.
Fuela Model features Nb. of Nb. of reactions species Thermoch emical property estimatio n THERM [154], [206,207]d THERM [154], [206,209] THERM [154], [206,209] THERM [154], [206,209] THERM [154] THERGAS [155] ND Software features Kinetic Mechanis rate m estimati generator c onb N.C.H. N.C.H. N.C.H. N.C.H. N.C.H. KINGAS [157] N.C.H. None None None None None EXGAS [151] None CHEMK IN modul e used SENKIN N.D.e HCT [210]g HCT [210]g HCT [210]g SENKIN PSR PSR SENKIN PREMI X PSR OPPDIF F PSR PSR PSR PSR OPPDIF F ICEh PSR AUROR A Flame Master HCPRj HCCIk OPPDIF F PSR Model applicability conditions Low High Low P Mod T T (1 at erate (50 (130 P m) 0 K) 0 K) (10 atm) Ref.

Methyl Butanoate

1219 1498 N.D.f 1545 [167] 1317

264 295 N.D.f 275

[208] [166] [167] [170] [171] [174] [146]

203 25

(20 atm)

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46

Methyl Crotonate Methyl Hexanoate

1516 1875 2440

301 435 401 531 383 3012

THERGAS [155] [208] + TH ERGAS [155] THERGAS [155] THERGAS [155] MHX [182] THERM [154]

N.C.H. N.C.H. KINGAS [157] KINGAS [157] N.C.H. N.C.H.

None None EXGAS [152,153] EXGAS [152,153] None None

[169] [182] [153] [153] [184] [142]

Methyl Heptanoate Methyl Octanoate Methyl Decanoate

3236 2781 8820

(1100 K) (1100 K)

713 NO prod.i 8820 + 10 5 2992 3231

125 3012 + 20 648 324

Skeletal mechanism derived from Herbinet et al. model [142] Mechanism from Herbinet et al. [142] and Smith et al. [211] Skeletal mechanism derived from Seshadri et al. model [188] THERGAS KINGAS EXGAS [155] [157] [152,153] THERGAS [155] N.D. KINGAS [157] N.C.H. EXGAS [152,153] None

Pyrol ysis

Study

[188] [212] [189] [190]

7775 10000

1247 350

PSR PSR SENKIN PREMI X PSR SENKIN PREMI X PSR SENKIN PSR

[213] [147]

2276

7086

THERM [154] THERM [154]l THERM

N.C.H.

None

[214]

MD5EN MD9EN

N.D.f N.D.f

N.D.f N.D.f

N.C.H. N.C.H.

None None

[143] [143]

18

nC16 (RME) MB + nC7 + PME (RME) B30 surrogate fuel (49% ndecane, 21% 1methylnaph tlene, 30% MO in mole) MDO MM MP MST and MO MST

1841 1472 7748

225 309 1964

[154]l THERGAS [155] THERM [154] THERGAS [155] and literature data [201]

N.C.H. N.C.H. N.C.H.

None None None

SENKIN PSR SENKIN PSR

(1030 K)

[197, 215] [216] [201

13,004 20,412 30,425 >17,000 43,444 20,000

2012 3061 4442 >3500 6203 >4800

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MP, MST, MO, MLO, MLN MP, MST, MO, MLO, MLN EP

13,000 786 N.D.

f

420 139 N.D. 115 117

f

THERGAS KINGAS EXGAS PSR [155] [157] [152,153] THERGAS KINGAS EXGAS PSR [155] [157] [152,153] THERGAS KINGAS EXGAS PSR [155] [157] [152,153] Extended work by Herbinet et al. [142,143] THERM N.C.H. None PSR [154] THERGAS KINGAS EXGAS PSR [155] [157] [152,153] Extended work by Herbinet et al. [142,143] THERM N.C.H. None PSR [154] SENKIN N.D. N.C.H. None PSR SENKIN THERM [154] THERM [154] THERGAS [155] N.C.H. N.C.H. KINGAS [157] None None EXGAS [152,153] HCT [210]g HCT [210]g SENKIN PSR

[213] [213] [213] [144] [213] [145]

[148] [167] [167, 171] [174, 203]

EB
a

1101 1035

See nomenclature for species names. b N.C.H.: non-computer-helped method: the rate constants for the reverse reactions kreverse were computed from the forward rate constants kforward and the equilibrium constants Kc calculated using the appropriate thermochemical data according to Kc = kforward/kreverse. c None: no mechanism generator was used for developing the kinetic models which were instead built hierarchically. d Updated information related to group values by Fisher et al. [208] was published later by Curran et al. [207]. e N.D.: No details mentioned. f Model derived from Fisher et al. proposal [208] with some changes, but resulting number of reactions and species involved are not mentioned in the manuscript. g HCT was used instead of CHEMKIN. h Internal combustion engine model (single zone). i NO formation (GRI-Mech 3.0 mechanism). j Homogeneous constant-pressure reactor model. k Homogeneous-charge compression-ignition model. l Herbinet et al. [143] also took the opportunity to mention openly that the activation energy for abstraction of secondary 1 H-atoms by HO radicals needed to be corrected from 3500 cal mol (as used in the initial version of MD oxidation model) 1 to 35 cal mol .

3.2. General kinetic scheme and classes of elementary reactions in the combustion process The general kinetic scheme and classes of elementary reactions used in the development of the detailed chemical kinetic mechanisms proposed in the literature for the oxidation of esters with aliphatic main chains in Cn, n 4, are similar to those established by Curran et al. for the oxidation of n-heptane and iso-octane [217,207]. Extension to alkyl-ester molecules was achieved by including the chemical information specific to the ester moiety. The resulting kinetic scheme is shown in Fig. 4 [142], whereas the classes of elementary reactions considered for the generation of alkyl-ester

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oxidation mechanisms are listed in Table 6. Note that the main changes to these elementary reactions in relation to the work by Curran et al. [207,217] are in the class of reaction 26, which is specific to esters [167], and in the chemical nature of the species hidden behind the notation R, R, Q, and X. The naming conventions adopted in Fig. 4 and Table 6 are as follows: R and R to denote alkyl or alkyl-ester radicals or structures and Q and X are used to denote CnH2n or CnH2nCOO species and structures.

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Figure 4. Primary oxidation reaction pathways common to alkyl esters (aliphatic main chain Cn, n 4) [142] Adaptation from Curran et al. work [217]. The labeled reactions (18) are further described in the main text. Table 6. Major classes of elementary reactions used as basement by oxidation mechanisms proposed in the literature (extension of the work by Curran et al. [207] and [217] to alkyl-ester oxidation).
1. Fuel-unimolecular decomposition 2. H-atom abstraction from the fuel (ester) 3. Alkyl or alkyl-ester radical decomposition 4. Alkyl or alkyl-ester radical + O2 to produce olefinic molecule + HO2 directly 5. Alkyl or alkyl-ester radical isomerization 6. Abstraction reactions from olefinic molecule by OH, H, O, and CH3 7. Addition of radical species to olefinic molecules 8. Alkenyl radical decomposition 9. Olefinic molecule decomposition 10. Addition of alkyl or alkyl-ester radicals to O2 11. R + RO2 RO + RO 12. Alkyl and alkyl-ester peroxy radical isomerization to hydroperoxy alkyl and hydroperoxy alkyl-ester radical (RO2 = QOOH) 13. RO2 + HO2 RO2H + O2 14. RO2 + H2O2 RO2H + HO2 15. RO2 + CH3O2 RO + CH3O + O2 16. RO2 + RO2 RO + RO + O2 17. RO2H RO + OH 18. RO decomposition 19. QOOH QO + OH (cyclic ether formation via cyclization of diradical) 20. QOOH olefinic molecule + HO2 (radical site to OOH group) 21. QOOH olefinic molecule + carbonyl + OH (radical site to OOH group)a 22. Addition of QOOH to O2 23. Isomerization of O2QOOH and formation of ketohydroperoxide and OH 24. Decomposition of ketohydroperoxide to form oxygenated radical species and OH 25. Cyclic ether reactions with OH and HO2 26. Unimolecular elimination involving a six-membered transition state and leading to the formation of ethylene and a carboxylic acid molecule for ethyl esters or ethylene and a shorter ester for methyl esters [167] a This class of reaction was most often neglected

As shown in Fig. 4, two main reaction pathways with a three-way branch on one pathway clearly stand out depending on the temperature range. First, the oxidation of the ester RH is initiated by the abstraction of a hydrogen atom (H-abstraction or metathesis) from RH (at low and high temperatures) and the unimolecular decomposition of RH (at high temperatures only), which leads to the formation of alkyl and alkyl-ester radicals R (reaction 1, Fig. 4). These radicals may follow 20

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either the high-temperature- or low-temperature-dominant pathway. At high temperatures (above 800 K), unimolecular decomposition by -scission is the dominant route and yields olefins or olefinic esters (stable molecules) as well as smaller radical species R (reaction 2, Fig. 4) with the contribution of isomerization reactions. Olefins and olefinic esters formed through these primary routes react through the same types of reactions as the fuel molecules and through other reactions specifically because of the presence of the double bond, such as the radical-mediated addition to the double bond and decomposition by retro-ene reactions leading to two smaller 1-alkenes through a sixmembered ring transition state [142]. At low temperatures (approximately 500600 K), the alkyl and alkyl-ester radicals R mainly undergo O2 addition, leading to alkyl and alkyl-ester peroxy radicals RO2 (reaction 3, Fig. 4), which react by isomerization to hydroperoxy alkyl and hydroperoxy alkyl-ester radicals QOOH (reaction 4, Fig. 4). At this point of the oxidation scheme, a three-way branch allows QOOH radicals to undergo three pathways, the first two pathways of which dominate at intermediate temperatures: a CO -scission decomposition to olefinic alkyl or alkyl-ester stable molecule plus HO2 (reaction 5, Fig. 4); a decomposition to cyclic ether plus OH (reaction 5, Fig. 4); or a second addition to O2 leading to hydroperoxy peroxy radicals O2QOOH (reaction 6, Fig. 4). The product of this second addition leads to OH and ketohydroperoxide species (reaction 7, Fig. 4), which undergo low-temperature branching reactions by decomposition into two radicals (reaction 8, Fig. 4) [141] and [142]. Thus, it can be clearly observed that at two points of the general oxidation scheme, intermediate radicals (R formed by reaction 1 and QOOH formed by reaction 4, Fig. 4) are involved in competitive reaction pathways that dominate at different temperature ranges and lead to chain reactions of different modes. Globally, these competitive reaction pathways belong to two classes: (i) unimolecular decomposition by -scission occurring at high and intermediate temperature, which leads to chain-propagation reactions that produce one radical flux (reactions 2, 5, or 5 in Fig. 4), and (ii) addition to O2 occurring at lower temperatures, which leads to chain-branching reactions that produce two radical flux (reactions 3 and 6 leading to reaction 8 in Fig. 4). This competition between branching channels and propagation channels may induce global variation in reactivity over some temperature ranges, as outlined in the following section. 3.3. Negative temperature coefficient and related low-temperature phenomena The negative temperature coefficient (NTC) region signifies a zone of temperature in which the overall reaction rate decreases with temperature (Fig. 5). This phenomenon is specific to lowtemperature oxidation processes and occurs usually around 500800 K. Some explanations can be directly deduced from the general oxidation scheme (Fig. 4). At low temperatures, chain-branching occurs mainly via the O2 addition reaction pathway, going through a ketohydroperoxide species (reaction 7, Fig. 4). As the temperature increases, the chain-propagation reactions of the QOOH species (reactions 5 and 5, Fig. 4) increase because the energy barrier for their formation is easily overcome, which leads to the formation of cyclic ether species and olefinic molecules at the expense of the reaction pathways through the ketohydroperoxide species (reaction 8, Fig. 4). The increasing importance of these propagation channels leads to a lower system reactivity, which is observed as the NTC region. However, propagation channels related to high-temperature -scissions should also partially contribute to these phenomena. Thus, NTC phenomena could be considered as a chemical transient regime that allows for continuously transitioning from established low- to hightemperature chemical regimes. This feature is commonly encountered in hydrocarbon combustion [207] and [217] and is observed when operating at engine conditions with esters comprised of aliphatic main chains in Cn, n 5 [172], where oxidation mechanisms may involve temperature rangedependent competition between chain-propagating channels and chain-branching channels.

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Figure 5. Illustration of the negative temperature coefficient region: experimental and computed conversions of methyl palmitate in a JSR as a function of temperature [143]. 3.4. Methyl ester kinetic studies Kinetic studies related to methyl esters are presented first for methyl butanoate (molecule firstly selected in the literature as biodiesel surrogate and thereafter considered as a mimetic molecule of the methyl ester function) and the corresponding ester with a double bond in the middle of the aliphatic main chain, i.e. methyl crotonate (methyl (E)-2-butenoate). Next, studies are presented for molecules tending toward suitable biodiesel surrogates (methyl hexanoate, methyl octanoate, methyl decanoate, methyl-5- and methyl-9-decenoate), then for actual biodiesel molecules (methyl myristate, methyl palmitate, methyl stearate, methyl oleate, methyl linoleate, and methyl linolenate), and ultimately for two commercial biodiesels (rapeseed and soybean oil methyl esters). 3.4.1. Oxidation of methyl butanoate as mimetic molecule of the methyl ester function As might be expected, methyl butanoate (MB) (C3H7(CO)OCH3) has been the subject of many published kinetic studies ([146,164-172,174,175,177-180,208], Tables 4 and 5 with regard to oxidation kinetics studies). This C4-methyl ester was originally selected as the mimetic model molecule of larger biodiesel components (C16- to C22-methyl esters, Table 1) to limit the number of possible products formed to a manageable level and to produce a reaction mechanism of a manageable size that can focus on the kinetic description of the methyl ester moiety. The main chemical structure features that account for the combustion characteristics of biodiesel, i.e. the ester moiety and aliphatic main chain of sufficient length, were thought to be conserved; thus, MB seemed large enough to allow the fast RO2 isomerization reaction (class of reactions 12 in Table 6; reaction 4 in Fig. 4) that play a key role in low-temperature chemistry and control fuel autoignition under conditions found in diesel engines. The first detailed chemical kinetic mechanism for the combustion of MB was developed by Fisher et al. [208]. This proposal comprised 264 species and 1219 reactions (Table 5) and was established by introducing the submechanism that described the specificity of MB oxidation to the existing oxidation mechanism for n-heptane by Curran et al. [217]. The model by Fisher et al. [208] was tested against the limited combustion data available at the time. These tests were conducted in closed vessels under low temperatures and subatmospheric conditions [218-221]. SENKIN software [222] was used to perform the chemical kinetic calculations in which the thermodynamic properties of the methyl esters and their decomposition products were estimated using Benson group and bond additivity methods [156] with updated values [206,207]. Some qualitative agreement was obtained; however, calculations consistently indicated higher overall reactivity by a factor of 1050 compared with experiments. In addition, according to the same experimental data, the Fisher et al. model [208] predicted a weak NTC behavior for MB oxidation that the authors explained using their proposed 22

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low- and high-temperature reaction pathways (Fig. 6). Obviously, part of the general kinetic scheme presented in Fig. 4 for alkyl-ester oxidation can be observed when applied to the MB molecule as this pathway is directly derived from Fisher et al., who presented the original idea. In particular, competition between chain-propagation channels (from unimolecular decomposition at high temperatures) and chain-branching channels (from O2 addition at low temperatures), which usually involves NTC phenomena, can be observed at two points of the Fisher et al. model (Fig. 6).

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Figure 6. Key low- and high-temperature reaction pathways of methyl butanoate oxidation for one of the four possible hydrogen abstraction sites (Fisher et al. model [208]). The three other possible sites of H-abstraction are on the carbon in or to the radical site illustrated in the figure and on the methyl group of the ester function. Later on, Marchese et al. [164] conducted MB oxidation experiments in a flow reactor operating under moderate pressures over low to medium temperatures with various equivalence ratios and a residence time set to a constant value (Table 4). Profiles of the reactant, intermediates and product species determined during the experiments were compared with simulation results obtained from the Fisher et al. [208] mechanism. Good agreement was obtained under stoichiometric conditions; however, the model overpredicted the experimentally observed reactivity under fuel-rich conditions and under-predicted reactivity under fuel-lean conditions. More recently, Gal et al. [166] proposed a revised version of the Fisher et al. mechanism [208], which was developed and validated based on the new experimental results they generated over a wide range of operating conditions using various pieces of equipment: a jet-stirred reactor (JSR), a Princeton variable pressure-flow reactor (VPFR), and an opposed-flow diffusion flame (OFDF) (Table 4). Molar fraction profiles for a large number of molecular species were obtained from JSR and VPFR experiments: MB and O2 (reactant); H2, CO, CO2, acetylene, methane, ethylene, ethane, propene, propane, formaldehyde, methanol, methyl propenoate, propanal, and methyl crotonate (major products); allene, acrolein, acetaldehyde, 1-butene, and 1,3-butadiene (minor products); and methyl vinyl ketone (trace compounds). Similar trends were observed for the profiles of the molecular species obtained from OFDF experiments. The new model by Gal et al. [166] consisted of 295 species and 1498 reactions. Three rate constant parameters from the original mechanism by Fisher et al. [208] were modified as described in Table 7, and a C4-submechanism taken from Dagaut et al. [223] was added to simulate the measured 1-butene and 1,3-butadiene profiles. The kinetic modeling is in reasonable agreement with the experimental results. However, under JSR conditions, MB reactivity 23

was under-predicted by the model at low temperatures. Concerning OFDF data, the same model generally showed higher reactivity for intermediate species and lower reactivity for MB than observed in experimental studies. However, the model accurately reproduced the VPFR data at stoichiometric conditions, and neither the model nor experiments showed evidence of the NTC region. It was only for the leanest investigated equivalence ratios that little NTC behavior could be observed between 600 and 800 K. Table 7. Reaction rate constants modified by Gail et al. [166] (bold) in the Fisher et al. mechanism for MB [208].a
Reaction A n Ea CH3CH2CH2(C=O)OCH3 + H. = H2 + CH3CH2.CH(C=O)OCH3 2.52E+14 0.00 7300 CH3CH2CH2(C=O)OCH3 + H. = H2 + CH3CH2.CH(C=O)OCH3 1.00E+14 0.00 7300 CH3O. (+M) = CH2O + H. (+M) 5.45E+13 0.00 13,500 CH3O.(+M) = CH2O + H.(+M) 1.38E+21 6.65 33,190 C2H3. + O2 = CH2O + HCO. 1.70E+29 5.31 6500 C2H3. + O2 = CH2O + HCO. 1.66E+13 1.39 1013 a n The rate coefficients are listed in the generalized Arrhenius form (k = AT exp(Ea/RT)) where units are mol, cm, s, cal, and K.

The same year, Metcalfe et al. [167] reported the oxidation of MB in a shock tube (ST). Ignition delay times were measured behind reflected-shock waves at two moderate pressures (1 and 4 atm) over the temperature range of 11001670 K for various equivalence ratios (Table 4). Their experimental results showed that at both pressures, the ignition delay times increased as MB concentration increased. Furthermore, the detailed mechanism proposed by the authors for MB oxidation was derived from the Fisher et al. model [208], and some changes were made as mentioned in the following. The H2/O2 mixture submechanism has been replaced with the mechanism published by O'Conaire et al. [224]. The bond enthalpy of the CH bond to a carbonyl group has been decreased to 93.6 kcal mol1 from 96.2 kcal mol1 because of quantum theory-based estimations by El-Nahas et al. [225]. Note that the value adopted by Metcalfe et al. [167] corresponds to the group additivity estimates and not to the ab initio calculations (94.2 kcal mol1) made by El-Nahas et al. [225]. The rate constants for MB radical decomposition have been adjusted to account for alkyl and alkoxyl radical decomposition according to the work by Curran [226]. The high-pressure limit rate constant expressions for unimolecular ester fuel decomposition reactions have been decreased by 66% (multiplied by 0.33). Unimolecular fuel decomposition reactions have been treated using quantum RiceRamsperger Kassel theory to account for pressure falloff (variation of the rate constant as a function of pressure). A six-centered unimolecular elimination reaction that yields ethylene and methyl ethanoate (methyl acetate) was added (Fig. 7) with an activation energy of 68 kcal mol1 [225]. However, the authors found that this last pathway (Fig. 7) contributed very little (<1%) to MB decomposition for the conditions investigated during the work.

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Figure 7. Six-centered unimolecular elimination for methyl butanoate producing methyl ethanoate and ethylene [167]. Following this work, measurements of ignition delay for MB were performed by Dooley et al. [170] at low temperatures (640949 K) in a rapid compression machine (RCM) and at higher temperatures (12501760 K) in a shock tube (Table 4). The autoignition of methyl butanoate was observed to follow the Arrhenius law ( = Aexp(E/RT)) over all conditions studied. The authors also proposed a detailed chemical kinetic mechanism, which is an extensively modified version from their previous work [167]. The main changes are listed below (an exhaustive description is presented in Dooley et al. [170]): Some bond enthalpy values originally presented in Fisher et al. [208] were reevaluated using THERM [154] with updated H/C/O and bond dissociation groups [206,209]. These values concern the nC3H7C(O)OCH3 and nC3H7C(O)OCH3 bonds reduced to 86.8 and 89.9 kcal mol1 from 101.2 and 92.0 kcal mol1, respectively. These values are in substantial agreement with the work by El-Nahas et al. [225], who proposed 87.0 and 93.4 kcal mol1, respectively, using ab initio calculations. A C4-submechanism (involving species with 4 carbon atoms) was added based on the work by Curran et al. [207,217] to account for C4 species observed in Gal et al. [166]. The low-temperature chemistry describing the isomerization of alkylperoxyl radicals to hydroperoxyl alkyl radicals (reaction 4, Fig. 4) was not included. This choice was motivated by the experimentally non-observed low-temperature reactivity. The new mechanism consisted of 275 species and 1545 reactions and was validated against the data generated by the authors (in RCM and ST) and those reported in the literature (in a flow reactor [164], a ST [167], a JSR and an OFDF [166]). The simulations were in good agreement with the experimental data selected. However, the agreement with the RCM ignition delays was less accurate. In addition, analysis of the kinetic model confirmed that different reaction pathways become prominent depending on the operating conditions, such as temperature, pressure, and equivalence ratio. In particular, the importance of unimolecular fuel decomposition at high temperatures (reaction 1, Fig. 4), the processes of the HO2 radical at low to intermediate temperatures (steps successive to reaction 5, Fig. 4), and the importance of fuel alkyl-radical decomposition (reaction 2, Fig. 4) under fuel-rich conditions were highlighted. In addition, from their results in shock tubes and RCM, Dooley et al. [170] concluded that MB did not exhibit NTC behavior. To meet the internal combustion engine conditions, Walton et al. [171] performed the experimental ignition of MB using an RCM over low temperatures (9351117 K) and moderate pressures (4.719.6 atm) (Table 4). The rate constants of some MB reactions from the Metcalfe et al. mechanism [167] were slightly modified to improve the agreement between the computed and experimental results. These reactions are presented in Table 8. Overall, the agreement between the computed and experimental results was excellent for all temperatures. In addition, the results support the assumption that MB consumption would be dominated by relatively slow bimolecular H-atom abstraction reactions.

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Table 8. Reaction rate constants modified by Walton et al. [171] from Metcalfe et al. mechanism [167] related to MB oxidation.a
Reaction A n Ea CH3CH2CH2(C=O)OCH3 + HO2. = H2O2 + .CH2CH2CH2(C=O)OCH3 1.90E+12 0.00 20,440 CH3CH2CH2(C=O)OCH3 + HO2. = H2O2 + CH3.CHCH2(C=O)OCH3 1.30E+12 0.00 17,690 CH3CH2CH2(C=O)OCH3 + HO2. = H2O2 + CH3CH2.CH(C=O)OCH3 1.30E+12 0.00 17,690 CH3CH2CH2(C=O)OCH3 + HO2. = H2O2 + CH3CH2CH2(C=O)O.CH2 1.90E+12 0.00 20,440 CH3CH2CH2(C=O)OCH3 + H. = H2 + .CH2CH2CH2(C=O)OCH3 1.88E+05 2.75 6280 CH3CH2CH2(C=O)OCH3 + H. = H2 + CH3.CHCH2(C=O)OCH3 1.30E+06 2.40 4471 CH3CH2CH2(C=O)OCH3 + H. = H2 + CH3CH2.CH(C=O)OCH3 1.30E+06 2.40 4471 CH3CH2CH2(C=O)OCH3 + H. = H2 + CH3CH2CH2(C=O)O.CH2 1.88E+05 2.75 6280 a The remainder of the mechanism from Metcalfe et al. [167] was unchanged. The rate coefficients are listed in the generalized Arrhenius form (k = ATnexp(Ea/RT)) where units are mol, cm, s, cal, and K.

Furthermore, Hakka et al. [174] performed an experimental and modeling study of the oxidation of MB and ethyl butanoate (EB) in a ST and a JSR. From the JSR experiments (operating conditions: atmospheric pressure at two moderate temperatures (800 and 850 K) for various residence times, Table 4), molar fraction profiles versus residence time could be generated for various molecular species: MB and O2, which relates the reactants; CO, CO2, methane (CH4), acetylene (C2H2), ethylene (C2H4), propane (C2H6), methyl acrylate (methyl propenoate), and methyl crotonate (methyl (E)2-butenoate), which relates the intermediates and final products. Concerning the new experimental data generated in the ST, ignition delay times were performed by recording OH emissions behind reflected-shock waves for various operating conditions (at moderate pressure over a large range of high temperatures (12502000 K) as well as in fuel-rich, stoichiometric and fuel-lean compositions, Table 4). A new mechanism for MB was proposed using the first version of EXGAS software [149-151] and extended to account for short ester reactants [174]. In addition, for this class of compounds, the bond enthalpy of the CH bond adjacent to the carbonyl group was taken to be equal to 95.6 kcal mol1, as proposed by Luo [227] for ethyl propanoate (EP). The mechanism of MB oxidation could be applied from low to high temperatures and involved 203 species and 1317 reactions (Table 5). The simulations were performed using SENKIN (for ST-related results) and PSR (for JSR-related results) modules of CHEMKIN software [158]. The authors reported that the agreement between the experimental and simulated ignition delays of MB was satisfactory. The same trend was observed with the ignition delay times previously measured by Metcalfe et al. [167] and Walton et al. [171]. Nevertheless, the kinetic model overpredicted MB consumption and production of CO and CO2 but under-predicted ethylene formation when compared to experimental results obtained in a JSR. However, the consumption of O2 and formation of CH4, methyl acrylate, and methyl crotonate were correctly reproduced. Reaction flux analysis performed under ST and JSR conditions (at 1370 and 800 K, respectively, and for 50% conversion in MB) showed that MB is mainly consumed by H-abstraction with H, OH, and HO2 radicals, which are the main contributors. Recently, to provide complementary data on MB autoignition, Akih-Kumgeh and Bergthorson [175] measured ignition delay times behind reflected-shock waves (by CH emissions) at moderate pressures (1.211.4 atm) and high temperatures (10601632 K) for various equivalence ratios in oxygen/argon mixtures (Table 4). Measurements were also performed for n-heptane as fuel (instead of MB) for comparison. The generated experimental results for MB were compared with simulations obtained using the modified version of the Fisher et al. model [208] by Dooley et al. [170] along with the Hakka et al. model [174]. CANTERA software by Goodwin [228] was used to model the shock tube ignition process as a constant-volume adiabatic reactor. The authors determined that MB and nheptane had comparable high-temperature ignition delay times under stoichiometric conditions; however, differences were observed under other conditions. In addition, good agreement was observed between the data generated by the authors and previously published data [167,174], while the two test models deviated somewhat [170,174]. The authors highlighted that the model by Dooley et al. [170] generally predicted longer ignition delays than the model by Hakka et al. [174], and the models were in good agreement at low temperatures with more pronounced deviations at 26

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higher temperatures. In addition, the two test models deviated from experiments under rich conditions (while good agreement was obtained under stoichiometric conditions). Yang et al. [180] studied the oxidation of three C5H10O2 ester isomers (MB, methyl iso-butanoate, and EP) in premixed flames using photo-ionization mass spectrometry and monochromated synchrotron radiation. Significant differences in the compositions of key reaction intermediates were observed and explained by performing kinetic analyses of the detailed kinetic models developed in this study. Dooley et al. [178] measured extinction limits of MB, n-heptane, and MB/n-heptane diffusion flames with nitrogen dilution in counter flow with air. They observed that MB diffusion flames have a much lower extinction strain rate than n-heptane diffusion flames and that the extinction strain rate of n-heptane/MB diffusion flames increases significantly as the n-heptane fraction is increased. The modeling study showed that the inhibiting effect of MB is due to the difference in the energy contents and to formation of hydroperoxy radicals that interfere with the chain-branching reactions involving H-atoms and OH radicals. Grana et al. [147] developed a lumped kinetic model for the oxidation and thermal decomposition of MB. This lumped model also contains the chemistry for other small esters: methyl formate, methyl acrylate and methyl crotonate which are intermediates formed in the oxidation of MB. The model was successfully validated against a large set of experimental data obtained in a wide range of operating conditions [164,166,170,171,174,177,179]. Thus, thanks to sustained efforts on the development of experiments and kinetic models for MB oxidation, rapid progress has been made in the understanding of the oxidation chemistry of the methyl ester function (COOCH3). Nevertheless, some refinements are still required in order to achieve a better agreement between the various prediction models and experimental results. An alternative would be to check the consistency both of the whole of the experiments and of the whole of the models, via close collaborations between research teams. 3.4.2. Pyrolysis of methyl butanoate Oxidation mechanisms at high temperatures include characteristic reactions of pyrolysis as a purely thermal process (for example, fuel-unimolecular decompositions or bimolecular H-abstractions from the fuel). Therefore, it is interesting to highlight some studies on ester pyrolysis, as they can be used as core partial sub-mechanisms to study the combustion of ester species. Farooq et al. [173] studied the high-temperature thermal decomposition of three methyl esters (methyl acetate, methyl propionate, and MB) in a ST by measuring the CO2 mole fraction timehistories during pyrolysis. Measurements were conducted at high temperatures (12601653 K) with high reactant compositions (favorable for H-abstractions) under low pressure (Table 4). It was observed that the CO2 yields during pyrolysis were high and not strongly dependent on the aliphatic main chain length of the methyl ester. The incorporation of the theoretical work by Huynh and Violi [229] into the Fisher et al. model [208] allowed Farooq et al. [173] to account accurately for the CO2 yields experimentally observed, except at the highest temperatures. The theoretical work by Huynh and Violi [229], using ab initio techniques, resulted in the development of a new computed kinetic sub-model for MB thermal decomposition, including pyrolysis and oxidation processes. The rate constants for the unimolecular and bimolecular reactions in the temperature range of 3002500 K were calculated using RiceRamspergerKassel-Marcus and transition-state theories, respectively. Because of the rather low barrier of the H-abstraction reactions between MB and the flame radicals H, HO, and CH3, Huynh and Violi [229] focused their work on this class of reactions. Thirteen pathways (Fig. 8) were identified for MB thermal decomposition initiated by H-abstraction reactions, which led to the formation of small species, such as CH3, C2H3, CO, CO2, and formaldehyde (H2CO). Kinetic simulation results for high-temperature pyrolysis showed that the H + MB reaction was the 27

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most important reaction in the initial stage of MB decomposition. In addition, the C(O)OCH3 = CO + CH3O reaction was determined to be the main source of CO formation. Recently Farooq et al. [176] completed their study about the pyrolysis of MB by measuring concentration time-histories of CO, CO2, CH3 and C2H4 using shock tube/laser absorption methods.

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Figure 8. The thirteen pathways for methyl butanoate thermal decomposition initiated by hydrogen abstraction reactions [229]. 3.4.3. Oxidation of methyl crotonate As biodiesel also contains fatty acid esters with one or two double bonds (CH=CH), it is important to understand their impact on combustion chemistry. Therefore, various studies were conducted on methyl (E)-2-butenoate, common name methyl crotonate (MC), corresponding to one unsaturated C4-methyl ester (CH3CH=CH(CO)OCH3), for which oxidation behavior can be compared with the corresponding saturated C4-methyl ester MB (CH3CH2CH2(CO)OCH3). In addition, these studies are helpful for increasing the amount of information related to MB oxidation because MC is an intermediate product formed during MB combustion [166,174]. In their comparative study of MC and MB oxidation, Sarathy et al. [168] performed experiments in an OFDF and a JSR. Details related to the operating conditions are given in Table 4. The mole fraction profiles of major intermediates, final products and reactants were measured. The authors observed that both fuel molecules had similar reactivity. Nevertheless, the experimental results showed that MC oxidation produced much higher levels of aldehydes (2-propenal and acetaldehyde: toxic products) and light unsaturated hydrocarbons (acetylene, propyne, 1-butene, and 1,3-butadiene: soot precursors) compared to MB. However, MB combustion had higher levels of ethylene (C2H4). In addition, MC produced benzene, which was not detected for MB oxidation, in OFDF. These results led the authors to conclude that unsaturated esters would have a greater tendency to form soot than saturated esters.

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Later, Gal et al. [169] continued Sarathy et al.'s [168] work by extending the oxidation experiments made in a JSR for MC and MB (at atmospheric pressure over the temperature range of 8501350 K and under stoichiometric conditions) to fuel-lean mixtures (Table 4). Furthermore, Gal et al. [169] used these new experimental results in addition to those of Sarathy et al. [168] to extend the version of the detailed chemical kinetic model they previously proposed for MB oxidation [166] to MC by adding several specific reactions (Table 9). The rate constants of the new added reactions were derived using analogous reactions that occur in the established MB model. The thermochemical properties of the new species were calculated using THERGAS software [155], while the transport quantities were estimated from species of similar size and structure. The new revised mechanism consisted of 1516 reactions involving 301 species (Table 5). Overall, the new kinetic model reproduced the experimental data fairly well and confirmed the conclusions experimentally observed by Sarathy et al. [168]. Table 9. Reactions added to the Gal et al. model [166] for representing MC oxidation [169].a
Reaction CH3CH=CH(C=O)O. + .CH3 = CH3CH=CH(C=O)OCH3 CH3CH=CH.C=O + CH3O. = CH3CH=CH(C=O)OCH3 CH3CH=CH. + CH3O.CO = CH3CH=CH(C=O)OCH3 .CH2CH=CH(C=O)OCH3 = CH2=CH.CH(C=O)OCH3 CH3CH=CH(C=O)OCH3 + .CH3 = CH3CH=CH(C=O)OCH2. + CH4 CH3CH=CH(C=O)OCH2. + H. = CH3CH=CH(C=O)OCH3 CH3CH=CH(C=O)OCH2. = CH3CH=CH.C=O + CH2O CH3CH=CH(C=O)OCH2. + .OH = CH3CH=CH(C=O)OCH3 + .O. CH3CH=CH(C=O)OCH3 + .CH3 = .CH2CH=CH(C=O)OCH3 + CH4 CH3CH=CH(C=O)OCH3 + H. = .CH2CH=CH(C=O)OCH3 + H2 CH3CH=CH(C=O)OCH3 + O2 = .CH2CH=CH(C=O)OCH3 + HO2. .CH2CH=CH(C=O)OCH3 + .OH = CH3CH=CH(C=O)OCH3 + .O. CH3CH=CH(C=O)OCH3 + .OH = .CH2CH=CH(C=O)OCH3 + H2O CH3CH=CH(C=O)OCH3 + HO2. = .CH2CH=CH(C=O)OCH3 + H2O2 .CH2CH=CH(C=O)OCH3 + H. = CH3CH=CH(C=O)OCH3 .CH2CH=CH(C=O)OCH3 + .O. = .CH=CH(C=O)OCH3 + CH2O CH3CH=CH(C=O)OCH3 + .OH = CH3CH=CH(C=O)OCH2. + H2O CH3CH=CH(C=O)OCH3 + H. = CH3CH=CH(C=O)OCH2. + H2 a The rate coefficients are listed in the generalized Arrhenius form cal. A n Ea 8.00E+13 0.00 0 6.00E+13 0.00 0 8.00E+13 0.00 0 4.00E+12 0.00 60,000 1.00E+12 0.00 7300 1.00E+14 0.00 0 5.01E+12 0.00 19,000 3.50E+11 0.00 29,900 1.00E+12 0.00 7300 3.70E+13 0.00 3900 3.00E+13 0.00 52,800 7.00E+11 0.00 29,900 3.00E+13 0.00 1230 1.50E+11 0.00 14,190 5.00E+12 0.00 0 1.58E+07 1.80 1216 3.00E+13 0.00 1230 3.70E+13 0.00 3900 (k = ATnexp(Ea/RT)) where units are mol, cm, s, K, and

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As for C5H10O2 isomers (MB, methyl iso-butanoate and EP, Section 3.4.1) [180], Yang et al. [181] performed the experimental and modeling study of the oxidation of three unsaturated C5H8O2 isomers: MC, methyl methacrylate and ethyl propenoate in a premixed flame (using tunable synchrotron vacuum ultraviolet photo-ionization mass spectrometry). The authors observed that the presence of the double bond in esters enhances the formation of oxygenated intermediates in flames. 3.4.4. Oxidation of model molecules suitable as biodiesel surrogates Although investigations related to C4-methyl esters helped to add the knowledge regarding the impact of the methyl ester group on combustion chemistry, the molecules that were first selected as biodiesel surrogates were determined to be unsuitable. In particular, no evidence of cool flame or NTC region (except for a few sources claiming weak NTC behavior [168,208]) was experimentally observed or predicted by modeling. Nevertheless, actual biodiesel components, as with long-chain alkanes, should show these two types of phenomena (indicating competition between temperaturedependent oxidation channels, Fig. 4). It is now admitted that this deficiency is encountered with C4-methyl esters because their aliphatic main chains are too short. In such circumstances, peroxy radicals RO2 (reaction 3, Fig. 4) react to yield hydroperoxy radicals QOOH (reaction 4, Fig. 4) via internal H-atom transfer through a cyclic transition state with high ring strain energy. Methyl

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hexanoate or methyl octanoate, and a fortiori methyl decanoate, methyl-5- and methyl-9-decenoate, were determined to be more suitable biodiesel surrogates (although their molecular structure prevents them from performing as well as actual biodiesel components [230]). 3.4.4.1. Oxidation of methyl esters from methyl hexanoate to methyl octanoate Dayma et al. [182] performed the study of the oxidation of methyl hexanoate (MHX) in a JSR at high pressure (10 atm) and over a range of low to high temperatures (5001000 K) at various equivalence ratios and a constant residence time (Table 4). Concentration (mole fraction) profiles of 23 species were measured (O2, H2, CO, CO2, formaldehyde, methane, acetaldehyde, ethane, ethene, acetylene, propene, propanal, propenal, 1-butene, 1-pentene, and unsaturated methyl esters from C4 to C7). Under the investigated operating conditions, the authors reported that MHX showed three main reaction regimes similar to large hydrocarbons: A cool flame zone (560660 K) characterized by fuel consumption at low temperatures and the production of small aldehydes and methyl hexenoates. A NTC zone (660760 K) where the total reactivity decreased with increasing temperature. A high-temperature zone (>760 K) with the total consumption of the fuel. This new set of experimental data was used by the authors to develop and validate a detailed chemical kinetic model for MHX oxidation, which consisted of 435 species and 1875 reactions (Table 5). The mechanism was generated using a hierarchical and systematic method. The first edifice was based on the comprehensive MB oxidation mechanism developed by Fisher et al. [208], which was added to a 1-butene submechanism validated under various experimental conditions [223]. Nevertheless, four reactions from the Fisher et al. model [208] were modified to obtain better predictions, particularly for ethylene (C2H4) and methyl-2-propenoate (CH2=CHC(=O)OCH3) profiles (Table 10). In addition, a submechanism of 551 reactions was implemented to model the oxidation of MHX and related compounds from low to high temperatures. For similar reactions, the rate constants were those proposed by Fisher et al. [208] for MB. Nevertheless, because of the larger length of the aliphatic main chain for MHX, some rate constants had to be taken from the literature using structurereactivity relationships (with computation of the reverse rate constants from the corresponding forward rate constants and appropriate equilibrium constants Kc = kforward/kreverse calculated from thermo-chemistry). Thermochemical data were taken from the Fisher et al. model [208] and estimated using THERGAS software [155] for species belonging to MHX submechanism. The kinetic modeling was performed using the PSR code of CHEMKIN [158]. The proposed kinetic model yielded good overall agreement with the experimental results. Using reaction path analysis (Fig. 9), the authors highlighted that the oxidation behavior of MHX was mainly controlled, over the investigated temperature and pressure ranges, by the weakness of the CH bond on the carbon adjacent to the methyl ester group. Dayma et al. [183] also performed the experimental and modeling study of the oxidation of MH in a JSR following the same strategy as the one used for MHX [182]. This study confirmed the conclusions that were drawn for MHX. HadjAli et al. [172] examined the autoignition of five linear methyl esters from butanoic acid to octanoic acid in a rapid compression machine (RCM) at operating conditions useful for compressionignition engine model validation (for low and intermediate temperatures (650850 K) and medium to high pressures (420 bar), and for stoichiometric mixtures and the same dilution of oxygen as in air; Table 4). Nevertheless, under the conditions investigated, the vapor pressures of methyl heptanoate and octanoate were too low to permit valid autoignition experiments. Therefore, the authors selected MHX for a full investigation of its autoignition properties, including the identification and quantification of the intermediate products at low-temperature oxidation. The oxidation scheme and overall reactivity of MHX were examined and compared to the reactivity of C4C7 n-alkanes under the same experimental conditions to evaluate the impact of the methyl ester function on the reactivity of the n-alkyl chain. The low-temperature reactivity of MHX that leads to the first stage of autoignition 30

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(cool flame event) was similar to n-heptane. However, the NTC region was located at a lower temperature than in n-pentane and n-butane. The authors also presented the main reaction pathways that led to the detected products (for the lighter species: acetic acid, propenal, 1-pentene, propanal, methyl acetate, butanone, and butanal; for the C4-C7 species: unsaturated methyl esters, methyl epoxy esters with 35 atom rings, and 5-butyl-1,3-dioxolane-4-one). Table 10. Reactions and rate constants modified by Dayma et al. [182] (bold) in MB Fisher et al. model [208].a
Reaction A n Ea C2H4 + .C(=O)OCH3 = .CH2CH2(C=O)OCH3 2.11E+11 0.00 3350 .CH2CH2C(=O)OCH3 = C2H4 + .C(=O)OCH3 2.00E+13 0.00 30,500 CH2=CHC(=O)OCH3 + H. = .CH2CH2C(=O)OCH3 1.00E+13 0.00 2900 .CH2CH2C(=O)OCH3 = H. + CH2=CHC(=O)OCH3 3.00E+13 0.00 37,500 CH2=CHC(=O)OCH3 + .OH CH2O + C2H3CO + H2O 5.25E+09 0.97 1590 CH2=CHC(=O)OCH3 + .OH .CH2C(=O)OCH3 + CH2O 4.00E+12 0.00 928 CH2=CHC(=O)OCH3 + .OH .O.CHC(=O)OCH3 + .CH3 6.90E+11 0.00 928 C2H4OH = C2H4 + .OH 1.293E+12 0.37 26,850 C2H4 + .OH = CH2O + .CH3 1.40E+12 0.00 3250 a The rate constants were expressed using the modified Arrhenius equation k = ATnexp(Ea/RT) with units cm, mol, s, K, and cal.

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Figure 9. Reaction path analysis for the oxidation of methyl hexanoate in JSR for two operating conditions (a) T = 950 K, = 1, = 1 s, and P = 10 atm; (b) T = 650 K, = 1, = 1 s, and P = 10 atm [182]. The thickness of the arrows is proportional to the importance of the reaction path. The framed products were quantified (dashed arrows mean a several-step production). Concerning oxidation of methyl octanoate (MOC) under atmospheric pressure, new experimental results related to concentration profiles of stable species (reactants, intermediates, and final products) were obtained by Dayma et al. [184] using two different types of equipment: in a JSR as a function of temperature (from 800 to 1350 K) and in an OFDF as a function of distance from the fuel port (Table 4). Experimentally, atmospheric MOC oxidation in the JSR does not show any cool flame 31

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or NTC behavior, whereas hot ignition occurs at approximately 800 K. A detailed kinetic model for MOC oxidation was developed in the study, including 383 species and 2781 reactions (Table 5). Based on a strong hierarchical structure, the kinetic model for MOC oxidation was derived from the model previously proposed by the same authors for MHX oxidation with some changes: (i) only the hightemperature chemistry was included because no cool flame was detected in the MOC JSR experiments and (ii) some rate constants were reevaluated and updated according to the most recent literature. These updates particularly concern H-abstractions with peroxy radicals, -scission by Csp3Csp3 bond breaking, CO bond rupture yielding methoxy, H-transfer through 5-, 6-, and 7membered ring transition states, the C0C3 submechanism as a whole, and unimolecular ignitions by CC bond rupture, the sensitivity of which increased with diminishing pressure. Indeed, MHX oxidation measurements and modeling were performed by Dayma et al. [182] under higher pressure conditions (10 atm) for which unimolecular initiations by CC bond ruptures were not sensitive. In addition to the transport property database used by Seshadri et al. [188], new values were estimated for stable C2C10 saturated and unsaturated methyl esters and their corresponding radicals by assuming that the transport properties were similar for saturated and unsaturated esters of the same chain length. Model validation for MOC oxidation was performed by the authors using the new measurements, which showed reasonable agreement between the simulation results and hightemperature experimental data. In addition, the reaction pathway proposed by Dayma et al. [184] for MOC oxidation was fairly similar to the pathway proposed by the same authors for MHX at 950 K and 10 atm (Fig. 9), with the same predominant routes. The model developed by Dayma et al. [184] was used by Rotavera and Petersen [185] to perform comparisons with ignition delay times obtained using a ST. A good agreement was obtained between the two sets of data at 1.5 bar for lean mixtures whereas the model was not able to reproduce the experimental ignition delay time for stoichiometric and rich mixtures at 1.5 and 10 bar. 3.4.4.2. Oxidation of methyl decanoate Szybist et al. [186,187] reported the autoignition behavior of methyl decanoate (MD) in a variable compression ratio (CR) octane rating engine charged with premixed MD and air. The spark plug was disabled for this study so that combustion could be initiated kinetically, and ignition occurred simultaneously at multiple points throughout the cylinder, as in HCCI combustion. The CR of the engine was adjusted over a range of 4.013.75 at multiple equivalence ratios (Table 4). During each CR sweep, the exhaust composition of CO, CO2, formaldehyde, and acetaldehyde was monitored using Fourier transformed-infrared (FTIR) spectrometry and condensable exhaust gas was collected for subsequent gas chromatography/mass spectrometry (GCMS) analysis. The authors observed that MD exhibited two-stage ignition with LTHR followed by the main combustion event or HTHR for sufficiently high compression ratios (CR 9.1). For lower compression ratios (CR 5.6), MD only underwent LTHR. GCMS speciation of the LTHR exhaust condensate revealed the formation of various classes of species, a selection of which are listed in Table 11. In addition to a number of saturated and unsaturated methyl esters with shorter aliphatic main chains than MD, a number of saturated oxo-methyl esters with an additional carbonyl group on the aliphatic main chain was also identified. This result revealed that the long-aliphatic main chain acts similarly to n-paraffins during LTHR, while the ester group remains intact. However, FTIR analysis revealed significant amounts of CO2 produced during LTHR. Based on the commonly established results, according to which oxidation of CO to CO2 does not occur under low-temperature conditions when hydrocarbon chains are present in the medium [231], the authors concluded that the CO2 produced by MD during LTHR was because of decarboxylation of the ester group. Thus, from FTIR and GCMS information, the decarboxylation of MD should not occur until the aliphatic main chain has been largely consumed by LTHR reactions, which incorporate the contribution of oxygen in the molecule. The authors highlight that the oxygen present in the fuel is used less effectively to remove carbon from the pool of soot precursors, which reveals that esters should reduce particulate matter emissions less efficiently than

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ethers because of the loss of CO2 directly from the decomposition of the parent molecule (and not by oxidation). This feature will be further discussed in Section 4.1. Table 11. Selected identified species from the low-temperature heat release exhaust condensate of methyl decanoate oxidation [186] and [187].a
Methyl esters Oxo-methyl esters 4-oxopentanoic acid methyl ester 2-methyl butanoic acid methyl ester Methyl hexanoate Methyl heptenoate 5-oxopentanoic acid methyl ester Methyl octenoate 5-oxohexanoic acid methyl ester Methyl octanoate 6-oxoheptanoic acid methyl ester Methyl nonenoate (isomers) 4-oxooctanoic acid methyl ester Methyl nonanoate 2-oxodecanoic acid methyl ester Methyl decenoate (isomers) 9-oxodecanoic acid methyl ester Methyl decanoate a Additional detected species: organic acids (from butanoic to decanoic acid), 2-nonanone, heptanal, nonanal, 5-methoxycarbonylpentan-4-olide (result of a cyclic ester being formed at the aliphatic chain with the methyl ester group remaining intact ).

In a complementary approach to the experimental work by Szybist et al. [186,187], Herbinet et al. [142] developed a detailed kinetic model for MD oxidation by combining the mechanisms previously proposed for n-heptane, iso-octane [217,207] and MB [208] with the low- and high-temperature chemistry specific to MD. Kinetic parameters and thermochemical properties were updated according to the recent literature, including quantum theory-based estimations. In particular, the C H bond dissociation energy (bond enthalpy) of the carbon atom adjacent to the carbonyl group has been updated according to El-Nahas et al. [225], which was previously performed by Metcalfe et al. [167] and Dooley et al. [170] (value adopted by Herbinet et al. [142] and obtained by El-Nahas et al. [225] from ab initio estimations: 94.1 kcal mol1). Based on the overall primary oxidation reaction pathways and reaction classes derived from the work by Curran et al. [207,217] and extended to methyl and ethyl esters (Fig. 4 and Table 6, respectively), the resulting mechanism proposed by Herbinet et al. [142] included 8820 reactions and 3012 species (Table 5). The large numbers of reactions and species result mainly from the fact that MD is not a symmetric molecule (unlike an nalkane). Also, numerous types of reactions were accounted for. In particular, the isomerization of RO2 to QOOH radicals in the low-temperature regime (reaction 4 in Fig. 4) was considered as proceeding through 5-, 6-, 7-, and 8-membered cyclic transition states yielding numerous permitted H-shifts. Model validation was conducted by comparing the computed results with various classes of experimental information ranging from low- to high-temperature regions: the only available experimental data for MD obtained in a motored engine [186,187] as well as with rapeseed methyl ester oxidation results in a JSR [197] and n-decane ignition in shock tubes [232]. The first two classes of experimental information yielding species profiles helped to highlight the model's ability to reproduce the chemistry of most products formed, particularly the early production of CO2 that is specific to biodiesel. This important feature of the mechanism was obtained because of the insertion of low-temperature reactions that lead to the formation of CO2. The majority of these reactions is listed in Table 12. Reactions 1 and 4 (Table 12) are uniquely derived from the methyl ester group in MD and would not occur in hydrocarbon oxidation. In addition, the authors noted that the kinetic parameters were updated according to the work by Glaude et al. [233] relative to dimethyl carbonate in reaction 4 of Table 12. Successive reactions from an alkyl-ester radical to the formation of CO2 through the OCHO radical were also suggested by the authors; they are reported in Fig. 10. As shown, one oxygen atom in CO2 is derived from the non-carbonyl part of the ester group, and the other oxygen atom is derived from the oxygen molecule involved in the addition reaction. Nevertheless, Hayes and Burgess [234] highlighted using quantum-chemistry theory (ab initio and density functional theory) that this proposed CO2 production pathway is but one hypothesis. Other peroxy radical reactions may contribute to or even dominate in MB oxidation. Moreover, CO2 production in large methyl esters may vary further from the pathway proposed for MB; the ring size 33

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of the transition state (resulting from the aliphatic main chain length) and the type of the H-atom abstracted both play a role in this process. Table 12. Main reactions leading to the formation of CO2 at low temperature (from MD oxidation model by Herbinet et al. [142]).
1. .OCHO (+M) = .H + CO2 + (M) 2. HOCHO = H2 + CO2 3. .OH + CO = H. + CO2 4. CH3OC.O = .CH3 + CO2

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Figure 10. Successive reactions from an alkyl-ester radical to the formation of CO2 via the radical OCHO (from MD oxidation model by Herbinet et al. [142]). In addition, Herbinet et al. [142] obtained results that were in good agreement with n-decane experiments in shock tubes (ignition delay times and OH profiles) with an NTC region occurring in the range 780920 K at 12 atm. This result shows that the reactivity of large methyl esters is similar to that of n-alkanes of similar size. Nevertheless, fine kinetic details, such as early CO2 production occurring at low temperatures during biodiesel combustion, can only be predicted by considering actual methyl ester fuels. Following this work, an experimental and kinetic modeling study of the extinction and ignition of MD in non-premixed, aerodynamically strained flows was investigated by Seshadri et al. [188]. These characteristics were investigated under such conditions because flame extinction in highly strained flows is an important problem in gas turbine engines and because fuel/air mixtures must be ignited in flows in internal combustion engines. Critical conditions of counter flow extinction and ignition were measured with a fuel stream comprised of vaporized MD in nitrogen and an oxidizer stream of air (Table 4). The detailed chemical kinetic model for MD by Herbinet et al. [142] unfortunately includes too large a number of reactions and species for direct use in current flame codes. Therefore, a skeletal mechanism was deduced from the detailed mechanism using the directed-relation graph method. The derived skeletal mechanism only included 713 elementary reactions and 125 species. Predictions of extinction and ignition of MD in non-premixed counter flows agreed with the experimental data. In addition, the authors noted that the derived skeletal mechanism showed the minor importance of the low-temperature chemistry under the considered counter flow conditions. The reaction chemistry of most importance was determined to be the high-temperature reactions of fuel decomposition, radical abstraction, isomerization, and radical decomposition. The formation and consumption of olefin intermediates with ester moieties were also found to be significant. The same year, Hoffman and Abraham [212] investigated ignition delay and NO formation rates for MD and n-heptane (mineral diesel surrogate) under conditions of varying O2 concentration by employing the CHEMKIN homogeneous constant-pressure reactor model and the homogeneous34

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charge compression-ignition engine model [235]. Ignition delay time was defined in this study as the time for the gas mixture to reach 1500 K in the homogeneous reactor. Calculations were performed in a wide temperature range (7001350 K) at two pressures (12.5 and 40 atm) using stoichiometric mixtures of fuel and air (21% in O2). Reduced O2 molar concentrations (18%, 15%, and 12%) were obtained by replacing a portion of the initial O2 oxidizer with N2. This procedure was adopted to simulate the dilution effect of exhaust-gas recirculation. The MD detailed chemical kinetic model proposed by Herbinet et al. [142] was used without any modification. Nevertheless, the GRI-Mech 3.0 mechanism [211], involving 105 reactions and 20 species, was added to predict NO formation (Table 5). Computed results led the authors to observe that reducing O2 concentrations increased ignition delay for all fuels. As previously observed by Herbinet et al. [142] for MD and n-decane, MD and n-heptane showed similar autoignition characteristics, but with the NTC region occurring in different temperature ranges (in the range 750900 K at 12.5 atm and 820950 K at 40 atm for MD and at 50 K higher for n-heptane). Ignition delays were roughly the same for n-heptane and MD in the NTC region; however, outside the NTC region, the delay for MD was 3060% shorter. The authors also highlighted the effect of pressure on the NTC region. They observed that at higher pressures, the NTC region shifted toward higher temperatures and became less pronounced (because of H2O2 dissociation in 2 HO at lower temperatures when pressure was increased). Furthermore, the addition of NO to simulate exhaust-gas recirculation reduced the ignition delay time. However, in practical applications, the increase in ignition delay because of lower O2 concentrations dominated any decrease because of NO addition. More recently, Sarathy et al. [189] performed the first combustion data for MD in an OFDF (Table 4). Among the experimentally determined species profiles, the production of C5C8 1-alkenes, which were formed after -scission of fuel radicals, was of particular interest. The production of lowmolecular-weight oxygenated compounds, such as formaldehyde, ketene, and isomers of C2H4O (acetaldehyde and ethenol) resulting from the decomposition of the ester moiety in MD, was also observed. Furthermore, the experimental data were used to develop a novel skeletal mechanism based on the approach of Seshadri et al. [188] with minor modifications of the detailed model proposed by Herbinet et al. [142]. Similar to Seshadri et al. [188], Sarathy et al. [189] observed that the consumption of fuel was dominated by high-temperature chemical reactions. The resulting skeletal mechanism (648 species and 2998 reactions) was first validated by the authors to reproduce the behavior of the improved version of Herbinet et al. model [142] when applied to a PSR operating at low temperatures (500950 K), elevated pressure (100 atm), and stoichiometric conditions and was successfully used to predict the OFDF measurements of MD (Table 5). This result highlights the effectiveness of the directed-relation graph method in producing a mechanism that is computationally practical for one-dimensional flame simulations yet also retains a level of chemical fidelity. To complete the work by Sarathy et al. [189], Glaude et al. [153] performed oxidation of MD in JSR at temperatures from 500 to 1100 K, including the NTC region, under stoichiometric conditions and atmospheric pressure (Table 4). Over 30 reaction products, including olefins, unsaturated esters, and some cyclic ethers, were quantified and successfully simulated through a new detailed chemical kinetic mechanism (Ref. [213] in Table 5) and automatically generated using a new version of EXGAS software extended to large methyl esters [152,153] (further details of this version are presented in Section 3.4.6). In addition, the proposed mechanism was revealed to be of the same accuracy level as the model by Herbinet et al. [142], which is based on the same general rules (Section 3.2) but used a different generation approach (Section 3.1.1). Furthermore, Ahmed [236] simulated the effect of MD addition to petrodiesel surrogates (nC7 or nC10 in solution with iso-octane) on combustion characteristics in a HCCI engine. Simulations were conducted using a new detailed chemical kinetic model developed by merging the MD mechanism proposed by Herbinet et al. [142] with reduced mechanisms for the hydrocarbon fuels [237] and [238], whereas the HCCI experiments were modeled using a zero-dimensional single-zone reactor model of CHEMKIN [158]. After a successful validation model against the shock tube data for each 35

pure component (nC7, nC10, iso-octane, and MD), the authors analyzed HCCI engine simulations and observed that combustion phasing (evaluated using CA50, the crank angle for 50% heat release) was increased up to an additional 10% by volume of MD into each petrodiesel surrogate, whereas larger additions of MD (beyond 12.5% by volume) showed almost negligible effects. The author highlighted that further investigation was needed to understand this behavior of MD reactivity. Very recently, two modeling studies were published in the literature. Divart et al. [214] developed a detailed kinetic model for the oxidation of MD. The model developed in this study was designed from the original oxidation framework of MD proposed by Herbinet et al. [142]. It was successfully tested against data from the literature [153,188,189,192,193] and was compared with other models from the literature [142,153] showing similar performances. As for MB, Grana et al. [147] developed a lumped kinetic model for the oxidation and pyrolysis of MD. Comparisons were performed using experimental data from the literature obtained in a wide range of conditions: temperature ranging from 500 to more than 2000 K, pressures up to 16 bar, and equivalent ratios from lean to pyrolysis conditions [153,177,190,192,193]. The validation showed that, despite the simplifications due to the lumping strategy, the model was able to reproduce the experimental measurements in pyrolysis as well as in an oxidation environment, in both the low-temperature regime and in flame conditions.

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3.4.4.3. Oxidation of methyl-5- and methyl-9-decenoate Although the Herbinet et al. model [142] was determined to be a powerful tool for predicting biodiesel combustion, methyl decanoate (MD), which the model was based on, has no double bonds, unlike most actual biodiesel components. Therefore, to capture the impact of this chemical specificity on biodiesel reactivity and further refine the kinetic model, the same authors [143] investigated the oxidation of two C10-methyl esters with a double bond located at different positions on the aliphatic main chain: methyl-5-decenoate (MD5EN) and methyl-9-decenoate (MD9EN). Because of the similar molecular structures of the selected biodiesel surrogates, the two detailed chemical kinetic sub-mechanisms for the oxidation of MD5EN and MD9EN were generated from the previous MD oxidation models by adding the low- and high-temperature chemistry specific to the unsaturated species (presence of double bonds, vinylic and allylic H-atoms). Both models for MD5EN and MD9EN oxidation were compared with rapeseed oil methyl ester experiments in a JSR [197]. It was observed that MD9EN performed better than MD5EN in reproducing the reactivity and mole fraction profiles of the major species. The computed ignition delay times for MD5EN and MD9EN were also compared, which showed that MD9EN was more reactive than MD5EN, particularly in the NTC region, and led to the conclusion that MD9EN would be a better biodiesel surrogate than MD5EN. The authors attributed the lower reactivity of MD5EN to more difficult isomerization reactions of peroxy radicals RO2 over the double bond because of its location in the middle of the aliphatic main chain. Thus, the authors [143] highlighted that it is actually the length of the continuously saturated carbon chain in the reactant that determines its reactivity because this chain sets the range of possible RO2 isomerization reactions. To obtain a detailed chemical kinetic mechanism that would be more representative of biodiesel fuels, Herbinet et al. [143] combined the three models of oxidation related to MD, MD9EN, and n-heptane in order to match the C/O/H content in actual biodiesels. The resulting blend surrogate model was used to simulate the rapeseed oil methyl ester experiments conducted in a JSR by Dagaut et al. [197]. The blend surrogate model performed slightly better than the model for MD9EN by reproducing the experimental mole fraction profiles of most species with good agreement. These results led the authors to recommend this blend surrogate model for simulating the combustion of biodiesel fuels regardless of their origin by adjusting the mole fractions of the three components in the surrogate blend.

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3.4.5. Pyrolysis of methyl decanoate As previously mentioned for MB pyrolysis (Section 3.4.2), thermal decomposition and oxidation studies are complementary and necessary to perform the validation of detailed kinetic models. This knowledge is especially important for biodiesel surrogates because the first reactions of diesel fuels in the combustion chamber are similar to a pyrolysis process, which lead to a high amount of unsaturated products and soot that are later oxidized in the flame front. Hence, Herbinet et al. [190] performed an experimental and modeling study of MD thermal decomposition in a JSR close to atmospheric pressure at temperatures ranging from 773 to 1123 K for various residence times (Table 4). In addition to H2, CO2, and small hydrocarbons from C1C3, the main reaction products were 1-olefins (from 1-butene to 1-nonene) and unsaturated esters with one double bond at the extremity of the aliphatic main chain (from methyl-2-propenoate to methyl-8-nonenoate). In addition, the formation of polyunsaturated species (1,3-butadiene, 1,3-cyclopentdiene, benzene, toluene, indene, and naphthalene) was observed at the highest temperatures. Comparison of pyrolysis with an nalkane of similar size to MD (n-dodecane) led the authors to observe that both molecules had similar reactivity (Fig. 11); the n-alkane produced more olefins while the ester yielded unsaturated oxygenated compounds. The detailed kinetic model for MD thermal decomposition (Table 5), which was generated from the latest version of EXGAS software [152,153], provided a good prediction of the JSR experimental data and showed through kinetic analysis that the retro-ene reactions (which were added to the secondary mechanism specifically for this work) play an important role in the consumption of 1-olefins and unsaturated methyl esters, particularly in low-reactivity conditions. Nevertheless, as retro-ene reactions consist of intra-molecular decomposition reactions into propene and smaller unsaturated esters through a concerted mechanism involving a six-membered cyclic transition state and transfer of an H-atom at the -position of the C=C double bond (Fig. 12), only species larger than methyl-4-pentenoate are concerned by this class of molecular reactions. Consequently, small unsaturated esters (such as methyl-4-pentenaote and methyl-3-butenoate) were overpredicted (by a factor of approximately 2), indicating that a pure radical mechanism is not sufficient for these species specifically and should be completed with molecular reactions.

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Figure 11. Conversion of methyl decanoate and n-dodecane pyrolysis in JSR versus temperature (a) and residence time (b). ( and : methyl decanoate experiments; and +: n-dodecane experiments; line: methyl decanoate simulations). Inlet mole fractions of n-dodecane and methyl decanoate are 0.02 and 0.0218, respectively [190].

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Figure 12. Retro-ene reactions illustrated with 1-octene and methyl-8-nonenoate [190]. 3.4.6. Oxidation of actual biodiesel molecules As mentioned previously (Table 1), methyl myristate (MM), methyl palmitate (MP), methyl stearate (MST), methyl oleate (MO), methyl linoleate (MLO), and methyl linolenate (MLN) are components of methyl biodiesels derived from vegetable oils. The first three species are saturated Cn-methyl esters with n equal to 14 (MM), 16 (MP), and 18 (MST), whereas the last three species are unsaturated C18-methyl esters with one (MO), two (MLO), and three (MLN) double bonds (CH=CH). MP, MO, MLO and MLN are found in varying amounts in the methyl esters of most vegetable oils, while MM is rather in trace amounts (Table 1).

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Among these large fatty acid methyl esters, MP and MO were first investigated experimentally in mixtures with n-decane [194,195] to simulate biodiesel fuel oxidation behavior when blended with petrodiesel. For MP, comparisons were also conducted with n-decane/n-hexadecane as a blended surrogate for petrodiesel fuels; indeed, n-hexadecane (selected as reference fuel for the CN test, Section 2.3.1.2) and the MP aliphatic main chain have the same number of carbon atoms. For all surrogate blends, experiments were performed in a JSR over a wide temperature range covering low and high temperatures (5501100 K) at quasi atmospheric pressure and stoichiometric conditions (Table 4). Numerous reaction products were identified and quantified [194,195], as will be observed in the following sections. On the basis of these measurements, detailed kinetic models of large methyl ester oxidation were later developed and validated (Table 5). Herbinet et al. [213] proposed oxidation mechanisms for saturated esters from methyl decanoate up to methyl stearate using the automatic generator in EXGAS software [152,153]. Naik et al. [144] and Westbrook et al. [145] proposed oxidation mechanisms for saturated and unsaturated C18-methyl esters using iterative generation from previous mechanisms developed for methyl decanoate [142] and methyl decenoates [143] that were appropriately extended to the larger alkyl chain esters (MST, MO, MLO, and MLN) with additional C=C bonds (two for MLO and three for MLN). Comparison of the observed results highlighted the similarities and differences in the oxidation of large n-alkanes and methyl esters as well as unsaturated and saturated methyl esters of similar size. On the basis of these observations, the researchers next determined the optimal surrogate blend and detailed kinetic models in terms of size and performance to simulate and predict reliably the methyl biodiesel combustion properties. These issues are briefly described in the following sections. 3.4.6.1. Methyl palmitate versus n-hexadecane [194] MP and n-hexadecane (nC16) showed similar reactivity and the same NTC behavior over the temperature range studied, which confirmed previously observed results by Herbinet et al. [142] for MD and n-decane. Furthermore, most of the observed species were formed with two surrogate blends, n-decane/MP and n-decane/nC16. These common products are small oxygenated species (carbon oxides, methanol, and acetaldehyde), small hydrocarbons (methane, acetylene, ethylene, and ethane), and 1-olefins. The products observed depended on the temperature of oxidation. At 38

high temperatures, the products were monounsaturated esters with the double bond at the extremity of the aliphatic main chain for MP (type A molecules, Fig. 13) and 1-olefins for nC16. At low temperatures, the specific products for MP were methyl esters with a cyclic ether group located on the aliphatic main chain and a 5-membered cyclic ether ring, including the ester group, branched to a long-aliphatic main chain (type B and C molecules, respectively, Fig. 13); regarding nC16, the specific products were 5-membered cyclic ether rings and ketones branched on an aliphatic chain with 16 carbon atoms. The first class of compounds that occurred at high temperatures were also observed by Szybist et al. [186,187] for MD, whereas for the second class of compounds that occurred at low temperatures, Szybist et al. observed oxo-alkanoic acid methyl esters and cyclic esters, probably because of the shorter aliphatic main chain of the ester MD (Table 11).

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Figure 13. Samples of molecules observed by Hakka et al. [194] during oxidation of the ndecane/methyl palmitate blend (species A observed at high temperatures, species B and C at low temperatures). 3.4.6.2. Methyl palmitate versus methyl oleate [195] Bax et al. reported that both molecules (MP and MO) exhibited similar reactivity with the NTC zone, occurring at approximately 650750 K. Nevertheless, because of the presence of the double bond in the middle of the aliphatic main chain for MO, specific reactivity features and reaction products were noted by the authors. First, MO appeared to be slightly less reactive than MP in the low-temperature range (below 750 K) despite two additional carbon atoms relative to MP, whereas the opposite trend was observed beyond the NTC region. The authors attributed this behavior to the presence of the double bond, which disfavored low-temperature chain-branching reactions, mainly the isomerization of peroxy radicals RO2 into hydroperoxy radicals QOOH (reaction 4, Fig. 4). Concerning the reaction products specific to MO oxidation, dienes and esters with two double bonds (resulting from decomposition by -scission of the two allylic radicals from H-abstraction of MO, Fig. 14) were observed at high temperatures (approximately 800 K). However, at low and intermediate temperatures (approximately 550650 K), oxygen-containing compounds were observed, namely aldehydes conjugated with one double bond (Fig. 15a) and C18-methyl esters with either one 3-membered cyclic ether functional group (oxirane esters, Fig. 15b) or one ketone functional group (oxo-esters, Fig. 15c) branched on the aliphatic main chain. These species were hypothesized to come from a combination of HO2 radicals with the resonance stabilized radicals from MO (conjugated aldehydes) or from the addition of HO2 or HO to the double bond in MO (leading to oxirane or oxo-esters, respectively). The authors concluded their work by highlighting that, based on recent investigations related to large methyl ester modeling [142,143], a detailed chemical kinetic model for MO generated by EXGAS software [152,153] would contain more than 50,000 reactions and 6000 species, making its application difficult.

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Figure 14. Illustration of dienes and esters with two double bonds formed during high-temperature n-decane/methyl oleate oxidation (species observed around 800 K and due to decomposition by -scission of the two allylic radicals resulting from H-abstraction of methyl oleate and stabilization by resonance) [195].

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Figure 15. Illustration of oxygen-containing compounds formed during low-temperature n-decane/methyl oleate oxidation (550650 K) and their possible channels of formation. (a) Aldehydes conjugated with one double bond; (b) C18-methyl esters with one 3-member ring cyclic ether functional group (oxirane esters illustrated here by 2-octyl, 3-(methyl octanoate)-oxirane); (c) C18-methyl esters with one ketone functional group (oxo-esters illustrated here by 10-oxo, methyl octadecanoate) [195]. 40

3.4.6.3. Methyl stearate versus methyl oleate, methyl linoleate, and methyl linoleate [144,145] The major refinements of the detailed chemical kinetic reaction mechanisms proposed by Naik et al. [144] (for MST and MO) and Westbrook et al. [145] (for the whole of these actual biodiesel components) in comparison with the work by Herbinet et al. [143] for the methyl decenoates (MD5EN and MD9EN) consist of three actions. The first (i) is to include accurate site-specific reaction rates for MO, MLO, and MLN as these species are products of oxidation of MST, MO, and MLO, respectively, and the major components of RME or SME (Table 1). However, olefins, di-olefins, and tri-olefins were treated as lumped species in the same way that the authors treated alkene and alkenyl radicals (reaction classes 69, Table 6) in past mechanisms for saturated hydrocarbon fuels [207,217] and the saturated methyl ester MD [142]. For the lumped olefins, di-olefins, and tri-olefins with the methyl ester group included, each species is assumed to react through H-atom abstraction reactions (with H, O, OH, HO2, CH3, CH3O, CH3O2, C2H3, C2H5, and O2), which produces a single lumped radical that is assumed to decompose to smaller species and eventually to small, usually unsaturated radicals, in the C1C4 core kinetic mechanism. The second action (ii) is to include MO in MST oxidation mechanism as a reactant (with reaction classes 15 in Table 6 but with some H-abstractions from allylic and vinylic sites as well as isomerization of the MO radicals, since both reaction types depend on the location of the double bond). Finally, the third action (iii) is to assume that RO2 and O2QOOH isomerization does not proceed in the low-temperature mechanism if a double bond is contained within the transition-state ring for the reaction (while in the mechanism by Herbinet et al. [143] for methyl decenoates, the double bond was assumed to contribute an additional 15 kcal mol1 to the energy barrier for these isomerization reactions). Action (ii) used the work by Naik et al. [144] related to MO oxidation that noted two very important features. First, radical addition to the C=C double bond contributes slightly to the overall rate of reaction; however, most of the MO consumption occurs through H-atom abstraction. Second, the rate of H-atom abstraction from the site adjacent to the carbonyl group is higher than abstractions from the secondary CH bond sites; however, abstraction from the allylic sites is even faster, whereas abstraction from the vinylic sites is much too slow to be important. Model validations for MP and MO [145] compared with the JSR experiments [194,195] showed good agreement over the entire temperature range for the fuel molecules and main products. These model validations also confirmed two specific features observed experimentally: (i) the formation of the species typical of fuel molecule oxidation (shown in Fig. 13 for MP and in Figs. 14 and 15 for MO) and (ii) the occurrence of a low-temperature reaction regime as well as higher temperature reactivity for the major reaction intermediates (1-olefins and 1-olefin methyl esters in MP oxidation). Recently, data computed with the model proposed by Westbrook et al. [145] were compared with ignition delay times of MO and MLO measured behind reflected-shock waves using an aerosol shock tube [196]. The comparison showed an under-prediction of the reactivity by about 50%. The thermochemistry of the fuels was refined resulting in significant performance improvements. Differences in the combustion properties between each methyl ester (MO, MLO, and MLN) were noted by Naik et al. [144] and Westbrook et al. [145] by performing simulations of oxidation in a JSR (Fig. 16) and a ST environment (Fig. 17) for each of the species individually considered. Concerning the JSR simulations (Fig. 16), the two saturated methyl esters, MP and MST, showed similar behavior with a pronounced low-temperature reaction zone and a small difference at approximately 750 K where MP showed slightly less conversion. However, the unsaturated methyl esters with one (MO), two (MLO) or three (MLN) CC double bonds showed significantly different behavior, particularly MLO and MLN. MO presented decreased low-temperature reactivity compared to its homologous saturated methyl ester MST but more fuel conversion for temperatures above 700 K, whereas MLO presented relatively little low-temperature reactivity with a small NTC region at 700 K, and MLN presented further decreased low-temperature reactivity with no NTC behavior. Concerning autoignition simulations (Fig. 17), all five methyl esters had nearly equal ignition delay times at high 41

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temperatures, which differed primarily at temperatures below 900 K, including the NTC region. While in this region, the two saturated methyl esters, MP and MST, showed nearly the same behavior, the ignition delay times of the unsaturated methyl esters were determined to decrease with the number of C=C double bonds. As MST, MO, MLO, and MLN have the same size and structure, except for the number of CC double bonds in the aliphatic main chain, differences in oxidation behavior observed in the low-temperature regime must be because of the occurrence of this bond, which also induces a decrease in CN. As highlighted by Westbrook et al. [145], the whole of these observations show a correlation between the chemical structure of the fuel molecule, cetane number, ignition delay, and low-temperature reactivity (only mentioned for the first three properties in Section 2.3.1.2). The authors conclude that fuels with greater amounts of low-temperature reactivity and heat release have shorter ignition delays and ignite earlier as well as have higher cetane numbers than fuels with decreased low-temperature reactivity. Naik et al. [144] concluded that this phenomenon was due to the C=C double bond that inhibits RO2 and O2QOOH isomerization when the C=C double bond is embedded in the transition-state ring, thereby reducing the overall rate of low-temperature chainbranching. These features will be observed again in the following section.

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Figure 16. JSR simulations carried out for five actual biodiesel components: methyl palmitate, methyl stearate, methyl oleate, methyl linoleate, and methyl linolenate. Operating conditions adopted for the simulations: stoichiometric fuel/oxygen, 0.2% fuel, with helium diluents, P = 1 atm, and residence time 1.5 s [145].

Figure 17. Ignition delay times for stoichiometric fuel/air mixtures in a reflected-shock tube environment at 13.5 bar initial pressure. Except asterisks showing experimental results for n-heptane/air, other results are kinetic model predictions: lines depict predicted values for each methyl ester fuel, circles for n-cetane (i.e. n-hexadecane), squares and diamonds for the surrogates SME and RME (Table 13) respectively [145].

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3.4.6.4. Determination of the optimal kinetic model in terms of size and performance for a reliable prediction of methyl biodiesel combustion properties With this objective, Herbinet et al. [213] developed detailed kinetic mechanisms for saturated esters from methyl decane (complementary to the work by Glaude et al. [153]) up to methyl stearate (from C10- to C16-methyl esters). These mechanisms, which were automatically generated using the latest version of the EXGAS software [152,153], include the reactions specific to the chemistry of large saturated esters and a single set of kinetic parameters. An exhaustive description of these refinements (and the general rules that led to them) is presented in the work by Glaude et al. [153]; therefore, the main features have just been briefly mentioned here. The changes concern both the primary mechanism (where the only molecular reactants considered are the initial organic compounds and oxygen) and the lumped secondary mechanism (consuming the molecular products of the primary mechanism). Regarding the primary mechanism, the changes affect the activation energies of four main classes of reactions: (i) unimolecular initiations, which involve the breaking of the CC bond located in the - and -position from the ester function (values were updated according to El-Nahas et al. ab initio estimations [225]); (ii) radical oxidations (yielding an unsaturated molecule and HO2) and H-abstraction from the carbon adjacent to the ester function (both classes of reactions were considered as if they concerned a tertiary H-atom); (iii) radical intramolecular isomerization reactions involving cyclic transition states with the embedded ester group; and (iv) radical decomposition by -scission involving the ester group for which quantum calculations were performed. Regarding the lumped secondary mechanism, the changes concern the new rules that had to be implemented for the consumption of the species formed specifically from ester oxidation in the primary mechanism. These new rules were based on the general idea promoting the formation of radicals via reactions that are already included in the primary mechanism (similar to Ref. [150] for alkanes). The performance of the MD model has been previously demonstrated by Glaude et al. [153] and model validation was achieved by Herbinet et al. [213] against the JSR experiments related to the MP species [194]. Very good predictions of the MP fuel reactivity and mole fraction profiles of most reaction products have been observed. In addition, as previously described for the MD species, predictions obtained for MP fuel were of the same level of agreement compared to experiments as those performed by Westbrook et al. [145], although both models are based on the same general departure (Section 3.2) but different generation approaches (Section 3.1.1). In addition to model validation, Herbinet et al. [213] compared the combustion properties of the selected methyl esters by individually simulating JSR oxidation of each fuel (Fig. 18). Moreover, to focus the comparison onto the molecular structure of the fuels, the inlet mole fractions were calculated to maintain a constant carbon content of each reacting mixture. All selected methyl esters exhibited similar conversion curves with an S shape because of the NTC (observed at 780 K, Fig. 18). In this region, the reactivity of the methyl esters increased when the length of the aliphatic main chains increased (from C10- to C18-methyl ester). Furthermore, the reactivity of n-hexadecane (also simulated by Herbinet et al. [213]) appeared to align the reactivity of the methyl esters with however a lower conversion in the NTC region and a slightly larger conversion at lower temperatures (below 750 K). Hence, Herbinet et al. [213] concluded that large n-alkanes, such as n-hexadecane, could be good surrogates for reproducing the overall reactivity of large methyl esters (as confirmed by Dagaut et al. [197] in next Section 3.4.7) with an important gain in computation time. Nevertheless, n-alkanes could not account for the formation of specific products, such as saturated esters or cyclic ethers with an ester function. Nevertheless, a mid-sized methyl ester, such as methyl decanoate, predicts the reactivity and molar fractions of most species fairly well with a substantial decrease in computational time and would be a good compromise as a biodiesel surrogate. Also, actual FAME components involve species with CC double bonds that induce specific changes in the combustion properties, as discussed previously [145]. Although Bax et al. [195] experimentally observed with MO fuel that the presence 43

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of a single C=C double bond in the middle of the aliphatic main chain had little effect on the reactivity of large molecules, this feature should not be observed for FAME with more embedded C=C double bonds, such as MLO (and MLN according to Westbrook et al. [145]). Therefore, one might conclude that an optimal biodiesel surrogate and optimal kinetic model would be selected depending on the objectives and applications.

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Figure 18. Comparison of the computed conversion of large saturated esters from methyl decanoate up to methyl stearate and n-hexadecane in a jet-stirred reactor [213]. 3.4.7. Oxidation of rapeseed and soybean oil methyl esters Pedersen et al. [239] performed a qualitative study of the species formed during the oxidation of rapeseed oil and RME in a stainless steel tubular reactor at 823 K. GCMS analysis of the two fuel gaseous emissions led the authors to conclude that rapeseed oil and RME react in a similar way during oxidation regarding the formation of hydrocarbons (1-alkenes, dienes, and benzene). Nevertheless, the authors observed that rapeseed oil oxidation produced high amounts of acrolein and other aldehydes, whereas RME oxidation produced significant amounts of methyl acrylate (methyl-2-propenoate) and other unsaturated esters, including methyl-3-butenoate, methyl-5hexenoate, and methyl-6-heptenoate. The formation of methyl-4-pentenoate was not observed. Quantitative investigation of RME oxidation was conducted in a JSR for the first time by Dagaut et al. [197]. The work developed by these authors was extensively used by researchers performing kinetic modeling investigations to validate their detailed chemical kinetic model on actual biodiesel oxidation experiments [142,143]. Details related to this significant experimental work are presented here. Experiments by Dagaut et al. [197] were conducted in dilute conditions over a wide range of temperatures (8001400 K), under low to moderate pressures (110 atm), and for various equivalence ratios and residence times (Table 4). Analysis of the mole fractions for measured species led the authors to observe a strong similarity between oxidation of RME and oxidation of large n-alkanes. The experimental species profiles were compared with computed mole fractions from a mechanism previously developed for the oxidation of n-hexadecane (nC16), which consisted of 225 species and 1841 reversible reactions [215] (Table 5). The agreement was shown to be satisfactory, and n-hexadecane appeared to be a good surrogate for RME under the investigated conditions. However, as it can be expected at this stage of the review, the nC16 mechanism was unable to predict the early production of CO2 that was observed in the experiments. According to assumptions reported by Szybist et al. [186,187], Dagaut et al. [197] suggested reactions responsible for this phenomenon but without giving further mechanistic considerations CnHm(CO)OCH3 CnHm(CO)O + CH3 CnHm(CO)O Cn1Hm2CH2 + CO2 (1) (2)

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Later, Dagaut and Gal [200] investigated the oxidation of a blend of RME and kerosene Jet-A1 (20/80 mol mol1) in a JSR. As far as the scope of this review with biodiesel fuels, only results related to RME oxidation will be reported. Experiments that were performed over a wide temperature range (740 1200 K) at 10 atm for various equivalence ratios and a constant residence time (Table 4) revealed the formation of monounsaturated methyl esters with a C=C double bond at the extremity of the aliphatic main chain (methyl-2-propenoate, methyl-3-butenoate, methyl-4-pentenoate, and methyl5-hexenoate). More recently, Golovitchev and Yang [216] developed an RME combustion model for internal combustion engine applications. By assigning methyl linoleate (C19H34O2) as model molecule for RME (although methyl oleate might be a better choice on the basis of the RME profile, Table 1), the authors based their RME combustion mechanism on the global decomposition reaction C19H34O2 + 0.5 O2 C5H10O2 + C7H16 + C7H8O (3)

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leading to products for which detailed oxidation sub-mechanisms were available in the literature. Species C5H10O2 representing MB was modeled with the Fisher et al. [208] mechanism, whereas C7H16 and C7H8O species, representing respectively n-heptane and phenyl methyl ether, were modeled with the Golovitchev's mechanisms [240]. The resulting biodiesel surrogate blend model produced a detailed RME combustion mechanism that consisted of 309 species and 1472 reactions, including soot and NOx formation processes, and was successfully validated using shock tube ignition delay data related to RME surrogate components (MB, n-heptane, and phenyl methyl ether). Nevertheless, for modeling and simulating diesel engine (Volvo D12C) combustion (using the KIVA-3V code [241]), the authors reduced the detailed mechanism to 88 species participating in 363 reactions. The simulation results showed that RME combustion could be achieved with low soot and NO concentrations if moderate exhaust-gas recirculation loads, which induced a reduction in the combustion temperature, were used. Recently, Westbrook et al. [145] applied the detailed chemical kinetic models they developed specifically for MST, MO (with the work by Naik et al. [144]), MLO, MLN, and MP to propose of a new reaction mechanism devoted to determine the differences in the combustion properties of two typical biodiesel fuels derived from soy and rapeseed oils (SME and RME, respectively). For this purpose, the authors combined the five methyl esters (MP, MST, MO, MLO, and MLN) into two different mixtures with composition approximating the SME and RME oils (Table 13) and performed oxidation simulation in a JSR (test 1 and test 2) and shock tube ignition (test 3) for these two 5-component biodiesel surrogates to validate the proposed reaction mechanism (Table 5). In addition, the same procedure can be extended to other methyl biodiesel fuels by specifying the convenient initial amounts of each of the five methyl ester components (MP, MST, MO, MLO, and MLN). Test 1. A comparison of the Westbrook et al. [145] reaction mechanism for the 5-component RME surrogate (Table 13) using the Dagaut et al. [197] experiments (related to RME oxidation in JSR) yields satisfactory overall agreement between the computed results and experimental values but with agreement for the profiles of the individual species varying from very good to marginal (particularly for H2). Test 2 and test 3. The differences in combustion properties between RME and SME fuels were highlighted by simulating JSR oxidation (test 2) and intermediate shock tube ignition (test 3) at the same operating conditions as the conditions used to validate the five methyl esters individually (Section 3.4.6). From the computed conversions of RME and SME surrogates in a JSR (Fig. 19), two important features were noted by the authors. First, all five components appeared to react together as opposed to sequentially; however, they reacted at rather different overall rates for the RME and SME surrogates. Second, the net low-temperature reactivity of the RME surrogate was determined to be significantly greater than the SME surrogate because of the difference in CN (CN being approximately 54 for the RME fuel and 47 for the SME fuel). This last result is in agreement with the difference in composition of the two surrogates and differences in CN of their prevalent 45

components (Table 13); the prevalent component in RME is MO, which is more reactive in the lowtemperature region than MLO, the prevalent component of SME. Nevertheless, nearly identical values of computed ignition delay times were obtained for the RME and SME surrogates; furthermore, these values were similar to the computed results for MO and MLO (Fig. 17). The differences in oxidation rates between RME and SME surrogates, which were greater in the atmospheric-pressure JSR simulations (Fig. 19) than in the high-pressure simulations related to shock tube ignition (Fig. 17), as well as the influence of pressure in the oxidation rates, were noted by the authors. Table 13. Composition of the two surrogate biodiesel blended fuels adopted by Westbrook et al. [145] for representing each actual SME and RME. Also shown are the measured cetane numbers (CN) for each of the fuel components [145].
Methyl esters Methyl palmitate (MP) Methyl stearate (MST) Methyl oleate (MO) Methyl linoleate (MLO) Methyl linolenate (MLN) Composition of the surrogate RME fuel 4.3 1.3 59.9 21.1 13.2 Composition of the surrogate SME fuel 610 25 2030 5060 511 Cetane number (CN) 86 101 59 38 23

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Figure 19. Computed comparison between oxidation of RME and SME surrogates in a simulated JSR. Operating conditions: stoichiometric fuel/oxygen, 0.2% fuel, with helium diluents, P = 1 atm, and residence time 1.5 s. The surrogate RME and SME compositions are taken from Table 13 [145]. In the continuity of their studies on MB [146] and MD [147], Saggese et al. [148] developed a lumped kinetic model for the pyrolysis and oxidation of biodiesel fuels. This model contains about 420

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species involved in approximately 13,000 reactions. Data computed with the lumped model were compared with data computed with the one proposed by Westbrook et al. [145] and experimental data from the literature [194,195,197-199] showing a reasonable agreement. 3.5. Ethyl ester kinetic investigations Research related to the oxidation of fatty acid ethyl esters (FAEE) is scarce, likely because commercial biodiesel components still consist of fatty acid methyl esters (FAME). Consequently, current research is still at the mechanism development stage for small model molecules that are known to be poor biodiesel surrogates but will provide significant information on ethyl ester oxidation behavior. In addition, the few published studies present oxidation results for FAEE by comparison with the studies for FAME, which highlights the advantages and disadvantages of both biodiesel alternatives as fuels. Therefore, the same approach will be adopted in this review for presenting the investigations in an effective way. The results will be first presented for ethyl propanoate and ethyl butanoate (versus methyl butanoate) and then for ethyl nonanoate (versus methyl nonanoate). The original tendency was to compare esters with the same chemical formula (isomers) while varying the length of the alkyl and aliphatic chains to investigate the effect of the molecular structure on the oxidation chemistry. Once different mechanisms were elucidated for various alkyl esters, the studies were devoted to compare the oxidation behavior of the functional groups, methyl esters and ethyl esters, for molecules with the same aliphatic main chain length. 3.5.1. Ethyl propanoate versus methyl butanoate Schwartz et al. [165] studied five different isomer esters with the chemical formula C5H10O2, including methyl butanoate (MB), methyl isobutyrate (MiBu), ethyl propanoate (EP), propyl acetate (PrAc), and isopropyl acetate (iPrAc). Their experiments were performed at atmospheric pressure in methane/air coflowing non-premixed flames separately doped with 5000 ppm of each ester (Table 4). These flames are typical of many practical combustors, especially soot-producing systems, such as diesel engines and gas turbines, and yet simple enough to permit a basic understanding. The mole fractions of the major flame species were measured using electron impact mass spectrometry. The authors determined that the main decomposition pathway in non-premixed flames for EP, as for acetate esters (PrAc and iPrAc), was a unimolecular-six-centered dissociation reaction, which led to a carboxylic acid and a 1-alkene (propanoic acid and ethylene for EtPr, eq. (4)). However, MB and MiBu, which cannot undergo a unimolecular-six-centered dissociation reaction, had decomposition rates that were consistent with a unimolecular CO fission mechanism, which generated two radicals (eq. (5) for MB). C2H5C(O)C2H5 C2H5C(O)OH + C2H4 C3H7C(O)CH3 C3H7C(O)O + CH3 (4) (5)

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The authors also observed propene (whose presence correlates to the formation of aromatics and soot) as a major decomposition product for all esters investigated. Nevertheless, EP and MB produced the lowest concentrations of propene, which is in agreement with the suggested primary reaction pathways (eqs. (4) and (5)). Simultaneously to MB (Section 3.4.1), Metcalfe et al. [167] also studied the oxidation of EP in a shock tube. For EP/O2/Ar mixtures, ignition delay times were measured behind the reflected-shock waves over a temperature range of 11401675 K at two low reflected-shock pressures and various equivalence ratios, including fuel-lean and fuel-rich conditions (Table 4). The authors reported that as EP concentrations were increased (from 1 to 1.5%) with the O2 concentration constant (at 6.5%), 47

ignition delay times increased. Conversely, increasing O2 concentrations (from 6.5 to 26.0%) with a constant EP concentration (of 1%) led to a significant reduction in delay times. The authors noted that this negative power dependence of O2 was in accordance with previous work on hydrocarbons [217]. Furthermore, because the chain-branching mechanism at the high temperatures investigated in their work (11401675 K) is due to the H + O2 = O + OH reaction, fuel-lean mixtures are more reactive in this regime (however, at low temperatures, because chain-branching is dependent on radical species formed directly from the parent fuel, fuel-rich mixtures are oxidized more quickly). Metcalfe et al. [167] also observed that EP was consistently faster to ignite than MB, particularly at low temperatures. Theoretical interpretation was applied to this behavior based on the detailed chemical kinetic mechanism they developed for the EP combustion. This mechanism contained 139 species and 786 reversible reactions, and the EP submechanism was built by analogy with MB (Table 5). However, some changes were made, which are mentioned in the following. The six-centered unimolecular elimination reaction that produces propanoic acid and ethylene, as previously stated by Schwartz et al. [165] (eq. (4)), has been added and characterized by an activation energy of approximately 50 kcal mol1 (Fig. 20). The EP mechanism contained the recently published H2/O2 submechanism by O'Conaire et al. [224]. As for the MB mechanism, unimolecular decomposition reactions were treated to account for pressure falloff. The ethylene submechanism was based on a previously published mechanism by Curran et al. [217]. The authors developed a propanoic acid submechanism based on the n-heptane and iso-octane kinetic mechanisms previously published by Curran et al. ([207,217], respectively). These changes led Metcalfe et al. [167] to perform simulations in good agreement with the experimental data. Also, production rate analyses achieved with the proposed mechanisms led the authors to explain the faster reactivity of EP (compared to that of MB) by the six-centered unimolecular decomposition which has a relatively low activation energy barrier and produces propanoic acid and ethylene (Fig. 20). According to the authors, it is the faster reactivity of these two products that is responsible for EP behavior.

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Figure 20. Six-centered unimolecular elimination for ethyl propanoate producing propanoic acid and ethylene [167]. Following this work for EP, Metcalfe et al. [202] recently performed JSR oxidation experiments that they used to further validate their previously proposed kinetic model [167]. Measurements were conducted under moderate pressure (10 atm), for various equivalence ratios and at temperatures in the range of 7501100 K (Table 4). Fuel (EP), intermediate and final product species were recorded as a function of temperature. The authors reported that the main intermediate species observed were ethylene, propanoic acid, formaldehyde, and methane, and ethylene and propanoic acid were the most abundant, whereas the major products were H2O, CO2, and CO. To obtain a better agreement with the profiles of the JSR species, the authors made some changes to the previously published EP oxidation mechanism [167]. The rate constant for the unimolecular elimination reaction EP = C2H4 + C2H5COOH was increased by a factor of four from 4.0 1012 exp(50,000/RT) to 1.6 1013 exp(50,000/RT) s1 (Ea in cal mol1). The rate constants for three abstraction reactions were decreased by a factor of two. These are listed in Table 14 with updated values of the rate coefficients.

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 An updated C3 submechanism developed by the authors and collaborators was incorporated. Table 14. Abstraction reactions for oxidation of ethyl propanoate as modified by Metcalfe et al. [202].a
Reaction A n Ea EP + HO2 = H2O2 + CH3 CH(CO)OC2H5 2.16E+12 0.0 14,400 EP + HO2 = H2O2 + CH3CH2(CO)OCHCH3 3.61E+03 2.5 10,530 C2H5COOH + HO2 = H2O2 + CH3 CHCOOH 2.16E+12 0.0 14,400 a n The rate coefficients are listed in the generalized Arrhenius form (k = AT exp(Ea/RT)) where units are mol, cm, s, cal, and K.

The revised mechanism was reported to be in good agreement with experiments (performed in JSR during this last study [202] and in an ST during the previous study [167]). Nevertheless, the authors observed better performance at stoichiometric and lean conditions than at rich conditions. In addition, the rate of production analysis led the authors to observe that the elimination reaction played a much smaller role in the decomposition of EP relative to H-abstraction under the JSR conditions compared to the ST ones. Furthermore, the sensitivity analysis highlighted the importance of ethylene chemistry on the overall reactivity of the system.

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Walton et al. [171] also performed low-temperature ignition of EP using an RCM (Table 4). The authors confirmed the observation made by Schwartz et al. [165] and Metcalfe et al. [167], according to which, EP ignited more rapidly than MB under the investigated conditions. The authors provided the same explanation of this reactivity as Metcalfe et al. [167] through the faster unimolecular decomposition of EP, which led to the formation of ethylene and propanoic acid. In addition, Walton et al. [171] proposed a new mechanism for EP oxidation based on the Metcalfe et al. [167] model that they improved to more closely match the experiments, particularly at low temperatures. The modified reactions and rate constants are summarized in Table 15. Table 15. Reactions modified by Walton et al. [171] from the Metcalfe et al. mechanism [167] for EP oxidation.a
Reaction A n Ea CH3CH2(CO)OC2H5 + HO2 = H2O2 + CH2CH2(CO)OC2H5 8.30E+03 2.55 16,490 CH3CH2(CO)OC2H5 + HO2 = H2O2 + CH3 CH(CO)OC2H5 1.50E+12 0.00 14,400 CH3CH2(CO)OC2H5 + HO2 = H2O2 + CH3CH2(CO)OCHCH3 2.50E+03 2.55 10,530 CH3CH2(CO)OC2H5 + HO2 = H2O2 + CH3CH2(CO)OCH2CH2 8.30E+03 2.55 16,490 a The remainder of the mechanism was unchanged from Metcalfe et al. mechanism [167]. The rate coefficients are listed in the generalized Arrhenius form (k = ATnexp(Ea/RT)) where units are mol, cm, s, cal, and K.

3.5.2. Ethyl butanoate versus methyl butanoate; ethyl pentanoate versus methyl hexanoate In a comparative study relating the oxidation chemistry of methyl and ethyl ester groups for which MB results have been previously reported (Section 3.4.1), Hakka et al. [174] investigated the autoignition of ethyl butanoate (EB) behind reflected-shock waves by setting the same operating conditions for both esters (Table 4). The results showed that ignition delay times increased when equivalence ratios were increased, which is in agreement with the Arrhenius-type empirical equation obtained by the authors, by correlating statistically the ignition delays versus temperature and concentrations in oxygen and fuel (s) = 1.88 1028exp(57,540/RT)[EB]0.250[O2]1.52 (6)

(with activation energy in cal mol1 and concentrations in mol cm3). The resulting equation also allowed the authors to note the obtained power dependences, which were strongly negative for O2 and small for EB. This phenomenon was also observed by Metcalfe et al. [167] for EP ignition in shock tubes. 49

Regarding the comparative analysis between MB and EB ignition, Hakka et al. [174] observed small differences in reactivity between both esters, except above 1600 K, where EB was observed to ignite slightly faster than MB. Furthermore, the higher reactivity of ethyl esters compared to methyl esters was also observed by Metcalfe et al. [167] for MB and EP but more prominently and particularly at lower temperatures. The difference in the extent of reactivity observed by both authors between MB and EB and MB and EP may be because, although all esters were in stoichiometric mixtures, MB and EP were introduced with the same molar fractions, whereas MB and EB having different molecular formula were not in the same molar fractions to maintain the same carbon atom concentration and C/O ratio (simulating molecules of pseudo-identical chemical formula). In such circumstances, comparison of the oxidation behavior between MB and EB highlights the impact related to the methyl and ethyl ester functional groups, whereas the same comparison between MB and EP highlights not only the impact related to methyl and ethyl ester functional groups but also differences in aliphatic main chain length. Hakka et al. [174] also proposed a detailed chemical kinetic mechanism for EB oxidation involving 115 species and 1101 reactions (Table 5). The mechanism was automatically generated using the same version of EXGAS software as the one used for MB [152,153,174]. Because validation through comparison of simulated and experimental results could be achieved by Hakka et al. [174] in shock tube conditions exclusively (because of the lack of other experimental information for EB oxidation at that time), this mechanism included only high-temperature reactions that were developed by analogy with MB. As reported by the authors, two significant changes resulted in differences with the MB mechanism: first, the inclusion of the molecular elimination reaction similar to that reported for EP by Metcalfe et al. [167] (Fig. 20) but leading for EB to the formation of ethylene and butanoic acid (BA), and second, the secondary reactions of BA for which new rules of generation were adopted. Considering the molecular elimination characteristics to ethyl esters, which is favored thanks to the six-membered ring transition state it proceeds through (Fig. 21), the authors adopted an activation energy of 47.3 kcal mol1 and an A-factor of 2 1012 s1 according to the measurements performed by Kairaitis and Stimson [242]. Regarding the secondary reactions of BA, these steps were automatically generated by considering this intermediate product as an initial reactant and developing a new detailed chemical kinetic submechanism for BA oxidation (built on a comprehensive primary mechanism and a secondary global chemical mechanism).

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Figure 21. Six-centered unimolecular elimination reaction for ethyl butanoate producing butanoic acid and ethylene [174]. The classes of elementary reactions used to build the primary mechanism related to the hightemperature oxidation of carboxylic acids are similar to those used in the case of methyl esters. However, the kinetic parameters of bimolecular reactions related to H-abstraction for the OH moiety of the carboxylic acid function were taken as equal to those of a tertiary alkylic H-atom [149]. The unimolecular initiation involving the breaking of the OH bond was also accounted for by the authors. The simulation (conducted with SENKIN module of CHEMKIN software [158]) showed correct agreement between the experimental and modeling results. In addition, reaction flux and sensitivity analyses helped the authors to further refine the arguments presented by Metcalfe et al. [167] for MB and EP oxidation behavior, according to which, the faster reactivity of the ethyl ester should be attributed to the faster reactivity of its oxidation products,

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such as carboxylic acid and ethylene. Hakka et al. [174] attributed the faster reactivity of EB compared to MB to the easier unimolecular initiation involving the production of branching agents (H radicals) through carboxylic acid formation (Fig. 22). Hence, the fact that this feature was observed particularly at high temperature (above 1600 K) was explained by the increasing importance of the unimolecular initiations with temperature. The authors also denoted from these analyses that the six-centered unimolecular elimination from EB decreased when temperature increased (this channel representing 75% of the EB consumption at 1370 K against 40% at 1635 K).

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Figure 22. Reaction flux analysis performed at 1370 K for an equivalence ratio of 1, and for 50% conversion of ester in the case of (a) methyl butanoate and (b) ethyl butanoate [174]. The size of the arrows is proportional to the relative flux. The channels involving a consumption of the esters below 5% are not shown. Dotted arrows represent several successive elementary reactions. These modeling results, including reaction flux and sensitivity analyses, were confirmed recently at medium and low temperatures by Bennadji et al. work [203] devoted to EB oxidation in a laminar tubular plug-flow reactor (PFR). The new experimental information (concentration profiles of the reactants, stable intermediates, and final products) was generated at atmospheric pressure over the temperature range of 5001200 K and under various dilutions, equivalence ratios, and residence times (Table 4). The authors used the model by Hakka et al. [174] without any significant modification for simulating the generated PFR data using the PSR module of the CHEMKIN computer package [158] (Table 5). The tubular PFR was modeled using a number of equivalent continuous perfectly stirred tank reactors (ePSR) in series, each uniform in composition, pressure, and temperature (the latter being attributed according to the temperature profile measured along the tubular PFR for each experiment). Bennadji et al. [203] reported a general agreement between the 51

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experimental and simulated results, which confirmed the validity of the model by Hakka et al. [174], although it was primarily performed based on high-temperature oxidation reactions. Bennadji et al. [203] also reported several additional features under the investigated conditions, briefly presented in the following. EB oxidation began at 800 K (with a significant reactivity in the 9001000 K range) for fuel-lean mixtures and for fuel-rich mixtures. In addition, BA and ethylene were the major products without observing ethyl acrylate formation (indicating that few H-abstractions would occur on the EB aliphatic main chain). These experimental observations, as well as the reaction flux and sensitivity analyses conducted on the PFR, led the authors to confirm that the main pathway of EB oxidation is the six-centered unimolecular elimination reaction that leads to ethylene and BA. Then, BA is almost entirely consumed by H-abstraction with H, OH, HO2, and CH3 radicals (metatheses), followed by -scission reactions to mainly produce acrylic acid through an REB-2 radical, as shown in Fig. 22b. This pathway is favored by the weakness of the CH bond in the -position to the carboxylic acid chemical function. High concentrations of CO coupled with low concentrations of CO2 were obtained under fuel-rich conditions, whereas the reverse situation was observed under fuel-lean conditions. Hence, the fraction of CO2 resulting from CO oxidation is added to the CO2 formed by decarboxylation of BA. In test conditions, decarboxylation of BA occurred at approximately 950 K, with almost complete consumption of BA at 1000 K, which suggests that BA decarboxylation should not occur until its aliphatic main chain has been largely consumed and incorporated oxygen in the molecule (similarly to large methyl esters as suggested by Szybist et al. [186] and [187] for MD oxidation). No NTC behavior was observed for EB, which is similar to MB [167] and [202] and demonstrates that EB is not an ideal surrogate molecule for a detailed study of ethyl biodiesel combustion; however, it should be regarded as a suitable model molecule for gaining insight into the oxidation chemistry of the ethyl ester functional group. Dayma et al. [204] performed the experimental and modeling study of the oxidation of ethyl pentanoate (also named ethyl valerate) in a JSR and in a spherical combustion chamber. JSR data obtained in this study were compared with experimental data obtained for MHX in similar conditions in the high-temperature region. Very similar reactivities were obtained for the two species in the contrary of smallest esters [167,174]. 3.5.3. Oxidation of model molecules suitable as biodiesel surrogates Given how investigations were conducted for methyl esters, researchers have realized that, although the work developed for the short esters has greatly helped the understanding of the chemistry of oxidation of the alkyl esters, only esters with long-aliphatic main chains exhibit the cool flame behavior that is characteristic of biodiesels. Hence, investigations moved forward directly from ethyl butanoate to long-aliphatic main chain ethyl esters. These investigations were not directed to the development of detailed chemical kinetic mechanisms for the oxidation of long-aliphatic main chain ethyl esters but rather to the generation of experimental information focused on applications related to modern engine designs, and from which it was possible, to propose major reaction pathways. This is the subject of the following subsections illustrated for ethyl hexanoate and ethyl nonanoate. 3.5.3.1. Ethyl hexanoate versus methyl heptanoate To examine the applicability of C8H16O2 ethyl and methyl esters as biodiesel surrogates for application in modern engine designs that employ low-temperature combustion strategies, Zhang and Boehman [205] performed an experimental study of the autoignition of ethyl hexanoate (EHX) and methyl heptanoate (MH) in a motored Cooperative-Fuel Research engine. For each test fuel, while operating 52

under fuel-lean conditions (equivalence ratio of 0.25) and at 600 rpm, the engine compression ratio (CR) was gradually increased from the lowest point (4.43) to the point where significant HTHR occurred. In addition, to draw the major low-temperature oxidation pathways for the two esters, the engine exhaust was sampled and analyzed using GCMS and GCFID/TCD at various CRs for which only LTHR occurred (Table 4). From the heat release analyses, the authors observed that EHX and MH exhibited an evident cool flame and experienced a transition from single-stage LTHR to two-stage ignition with the increase of the engine CR, which led to the conclusion that these two esters are likely suitable biodiesel surrogates in terms of low-temperature oxidation characteristics. Furthermore, at a given CR, EHX was determined to have a later onset and lower magnitude of LTHR compared to MH, which indicated that EHX is less reactive in the low-temperature region compared to MH (Fig. 23). The authors attributed this feature to the different aliphatic main chain lengths between the two esters.

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Figure 23. Comparison in heat release profiles between methyl heptanoate (triangle) and ethyl hexanoate (rhombus) at CR = 7.05 [205]. n-Heptane (round) was also introduced by the authors for illustrating that the presence of ester moiety inhibits low-temperature reactivity. Indeed, n-heptane and methyl heptanoate have the same carbon chain length and yet n-heptane experiences two-stage ignition while both esters only exhibit single-stage at the operating CR. Based on the literature mentioned above, this result appears to be in contradiction with the experimental and simulated observations previously performed by other researchers on the oxidation of EP and MB at high and low temperatures [165,167,171,202]. Hakka et al. [174] reported intermediary conclusions during their comparative study relating autoignition behavior between EB and MB (both esters reacted equivalently from 1280 to 1600 K; however, beyond this temperature range, EB reactivity was determined to be more prominent). Similar to EP and MB, EHX differs from MH in one CH2 group on the aliphatic main chain in addition to the nature of the ester functional group (ethyl or methyl ester group). Nevertheless, a significant difference between EP and MB and EHX and MH is that the first class of esters accounts for short esters, whereas the second class accounts for long esters; however, no evident relationship between this structure-based feature and reactivity with a critical length of the aliphatic main chain has been highlighted. Moreover, the differences between the chemistry of oxidation at low and high temperatures should also be accounted for in this evaluation. As a result, it appears that understanding reactivity order between ethyl and methyl esters against temperature requires more investigation. Concerning the results obtained by Zhang and Boehman [205] relating the exhaust species produced under engine conditions where only LTHR occurred, GC analyses showed that the aliphatic main chain of the two esters EHX and MH experienced the typical paraffin-like low-temperature oxidation sequence with the formation of unsaturated esters, epoxy esters, oxo-esters, aldehydes, and

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carboxylic acids. Similar to Dayma et al. [182], the authors also observed that the abstraction of Hatoms on the -carbon of the ester carbonyl group, further involving the cleavage of the CC bond to the ester carbonyl group to form alkyl (ethyl or methyl) propanoate, played an important role in the oxidation of long-aliphatic main chain esters. Moreover, in the case of EHX oxidation, a higher concentration of ethylene was observed compared to MH, with the additional formation of hexanoic acid, all confirming the existence of the six-centered unimolecular elimination reaction during lowtemperature oxidation of ethyl esters as previously reported by Schwartz et al. [165], Metcalfe et al. [167,202], and Walton et al. [171]. Based on these observations, the authors proposed major lowtemperature oxidation pathways for EHX (Fig. 24). As expected, this scheme is similar to the one adapted from Curran et al. [217] and Herbinet et al. [142] for the high- and low-temperature oxidation of methyl esters (Fig. 4). The difference is the insertion in the low-temperature channels of the unimolecular decomposition of the RH ester into a carboxylic acid and ethylene as well as with two additional decomposition paths of the hydroperoxy alkyl-ester radicals (QOOH), which were prominent at intermediate temperatures and formed either unsaturated esters with a terminal double bond, aldehydes and hydroxyl radicals, or oxo-esters and hydroxyl radicals. These two last reaction pathways were proposed with slight differences by Bax et al. [195] for MO oxidation.

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Figure 24. Major low-temperature oxidation pathways of ethyl hexanoate [205]. 3.5.3.2. Ethyl nonanoate versus methyl nonanoate To gain insight into the low-temperature oxidation of fatty acid esters produced from different alcohols with unsaturation sites located at different positions in the aliphatic main chain, Zhang et al. [1] experimentally investigated with the same engine environment as that used by Zhang and Boehman [205] the premixed ignition behavior of four C9 fatty acid esters: methyl and ethyl nonanoate (MN and EN, respectively) together with two monounsaturated methyl esters, methyl-2and methyl-3-nonenoate (MN2EN and MN3EN, respectively) (Fig. 25). Attention was focused on understanding the primary reaction pathways responsible for early CO2 production during the lowtemperature oxidation of fatty acid esters, as this process is directly linked to the reduction of soot formation. This point is discussed in further details later on (Section 4.1).

Figure 25. Molecular structures of the four C9 esters investigated by Zhang et al. [1]. aThe carbon atom of the carbonyl group is carbon no. 1. Carbon no. 2 corresponds to the -carbon of the carbonyl group. bThe -carbons of the ethylenic bond correspond to the carbon no. 2 and carbon no. 5 for methyl-3-nonenoate.

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Following the same experimental operating conditions and procedures as those adopted by Zhang and Boehman [205], Zhang et al. [1] reported that the four tested C9 fatty acid esters showed different ignition behavior using exhaust species analyses; MN and EN exhibited evident cool flame behavior and experienced two-stage ignition, whereas MN2EN and MN3EN experienced only single-stage ignition. The magnitude of LTHR was observed to follow the order EN > MN MN2EN > MN3EN. Furthermore, the comparison in percent of LTHR (defined as [LTHR/(LTHR + HTHR)] 100%) revealed that EN has the highest fraction of LTHR, which indicates that EN has the highest lowtemperature oxidation reactivity among the tested fuels. As discussed in the previous subsection, the higher low-temperature reactivity of the ethyl ester compared with methyl ester has been previously reported by various authors [165,167,171,202], who also explained this feature by the presence of the six-centered unimolecular elimination reaction of fatty acid ethyl esters that likely facilitate ignition because of relatively low activation energy. A second argument, also based on the structure reactivity relationship, was presented by Zhang et al. [1] but this one being relative to the presence of additional secondary CH bonds in the ethyl ester group. These might enhance the internal H-atom shift and form more seven-membered transition-state rings of low activation energy (analogous to six-membered transition-state rings [243]), contributing thus to a higher oxidation rate of the ethyl esters at low temperature. Nevertheless, it is worth mentioning that a reversed trend for the low-temperature oxidation reactivity was concluded for ethyl hexanoate (EHX) and methyl heptanoate (MH) by Zhang and Boehman [205], likely because of the difference in the length of the aliphatic main chain of the two esters. Therefore, further investigations relating this subject appear to be necessary to draw clearer conclusions and determine whether a critical length of the aliphatic main chain actually exists from which ethyl esters begin to be more or less reactive than methyl esters, depending on the temperature regime. Concerning the decreased oxidation reactivity of the unsaturated fatty acid esters in the low-temperature regime, the authors attributed this feature to the reduction of the possible number of six- or seven-membered transition-state rings that could be formed during the oxidation because of the presence of a double bond in the aliphatic main chain. The same conclusion was highlighted later by Naik et al. [144] and Westbrook et al. [145] when simulating MO, MLO, and MLN oxidation in a JSR. Moreover, Zhang et al. [1] deduced from the observed products that the inhibition effect of the double bond on the low-temperature oxidation reactivity of fatty acid esters became more pronounced as the double bond moved toward the central position of the aliphatic main chain. These trends were also observed later by Herbinet et al. [143] for methyl-5- and methyl-9-decenoate. Moreover, GC analysis of exhaust condensates, collected under engine conditions where only LTHR occurred, led Zhang et al. [1] to deduce that the aliphatic main chain of the saturated fatty acid esters (EN and MN) participated in typical paraffin-like low-temperature oxidation sequences with the formation of the same classes of products as those observed for EHX and MH [205]. In contrast, the unsaturated fatty acid methyl esters (MH2EN and MH3EN) were observed to exhibit olefin-like autoignition behavior (with the double bond in the aliphatic main chain being attacked by either hydroxyl or hydroperoxy radicals, which eventually led to the formation of either methyl esters with a terminal double bond and aldehydes or cyclic ether methyl esters and hydroxyl radicals). For all tested compounds, the ester functional group remained largely intact during the early stage of oxidation. Furthermore, the authors concluded from observed products for MN2EN and MN3EN oxidation that the presence and position of the double bond in the aliphatic main chain of the fatty acid esters could affect the primary route for early CO2 production. For MN3EN, it was suggested that early CO2 production might come from the direct decomposition of the methoxy carbonyl radical (CH3OCO) according to reaction pathway no. 4 in Table 12 [142]. However, it was proposed that MN2EN might experience the production of the radical CH2(CO)OCH3, which could follow the reaction pathway illustrated by Fig. 10 to form CO2 at low temperatures [142]. Finally, the authors observed that the 55

extent of CO2 production in the low-temperature regime followed the order: EN MN > MN2EN > MN3EN. 4. Outstanding issues and future refinements Experiments will always be the tools of choice for generating databases that are essential for the development and validation stages of modeling. Reciprocally, modeling enhances the efficiency of experimental studies by limiting unsuccessful trials by predicting the most appropriate conditions that will converge toward the desired objectives. Therefore, efforts in data generation using meaningful experiments and development of advanced kinetic models are worth pursuing to capture/predict key combustion behavior with higher accuracy. Nevertheless, one must keep in mind that the kinetic models will likely be used in addition to techniques based on multidimensional computational fluid dynamics (CFD) for optimizing the engine technology through 4-D simulations. In addition, the fuel oxidation mechanism should also merge with pollutant formation pathways, such as those relative to NOx [125], which still remain a difficult task because NOx formation is influenced by combustion chemistry and physics. As expected, the price for increasing accuracy at the kinetic modeling stage is a larger mechanism, by either including further elementary reactions or increasing the complexity of the surrogate fuel (in terms of chemical structure or number of components). As an example, the mechanisms presented by Naik et al. [144] for MST and MO consist of over 3500 chemical species and 17,000 elementary reactions while the mechanism by Westbrook et al. [145] for biodiesel fuels (developed considering biodiesel surrogates with five FAME) contains more than 4800 chemical species and nearly 20,000 elementary reactions. However, the size of the mechanisms induces computational costs that may compromise their combination with CFD techniques, operating at a different time scale. Naik et al. [144] and Lai et al. [35] noted that incorporation of a kinetic model into a multidimensional CFD application will require some degree of future mechanism reduction or simplification. In other words, for coupling chemical kinetics and CFD, an optimal compromise between the size of mechanism and computational costs is necessary. Accordingly, three alternatives are possible: (i) search of an ideal surrogate fuel that would be a satisfactory compromise between a representative mixture of actual biodiesel fuels (based on chemical and physical properties) and model molecules that allow for combustion simulations in a reasonable time (with a chemical structure encompassing an aliphatic chain length not too large and a reduced number of C=C double bonds in addition to an ester group); (ii) mechanism reduction (requiring a parent mechanism and experimental data for validation [35]); and (iii) the use of a detailed kinetic mechanism as an accurate data generator for predicting the desired operating conditions of an engine, which would be regressed using a numerical model for use within a CFD simulator. Nevertheless, it can be expected that the next steps in model development will be refinements and corrections of errors, not significant growth in the size of the mechanisms (even when considering new-generation alternative fuels comparable in molecular complexity to the biodiesel fuels already addressed). Other outstanding issues and future refinements in relation with pollutant emissions and future engine technologies remain, some of which are briefly described in the following. 4.1. CO, CO2 formation and soot reduction The main pathways of CO and CO2 formation proposed in the literature in terms of the oxidation and pyrolysis of methyl and ethyl esters are summarized in Fig. 26. As can be observed, these general pathways are identical for pyrolysis and oxidation processes as well under high and low temperatures, except for methyl ester pyrolysis at elevated temperatures (P1P2, Fig. 26). This latter pathway was also suggested for ethyl esters regardless of the process (pyrolysis or oxidation) and temperature conditions (low or high) because of the formation of the carboxylic acid as an 56

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intermediate product with a weak C(O)OH bond for this class of esters. This feature was also noted by Bennadji et al. [203] using reaction flux analysis conducted for EB oxidation in a PFR (Fig. 27).

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Figure 26. Main pathways of CO and CO2 formation proposed in the literature via pyrolysis or oxidation of methyl and ethyl esters under low- and high-temperature conditions. aP5 was taken into account for MB oxidation by Bennadji et al. [203], however sensitivity analysis showed that this reaction had very little impact into the process. bDashed arrows mean several successive reactions. Therefore, according to the general scheme presented in Fig. 26, CO and CO2 formation derived from the decomposition of the fuel molecule through chain-propagation channels with the initial step proceeding through either unimolecular reactions (P1) or bimolecular H-abstraction reactions (first step of P3 and P4). The unimolecular route leads to two radicals, R1 and R(CH2)3C(O)O, the latter yielding CO2 by -scission (P2). Regarding the bimolecular route, H-abstraction reactions mainly occur at position 3 or 4 of the carbonyl group (resulting in the fuel radicals Rfuel-3 or Rfuel-4, respectively),

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followed by successive -scission reactions, which lead to an olefin and either C(O)OR1 radical (last step of P3) or CH2C(O)OR1 radical (last step of P4). These two radicals are actually key species responsible of the production of CO and CO2. Radical CH2C(O)OR1 may undergo two channels of decomposition, which lead to either CO through successive -scission reactions (P10) or CO2 through various low-temperature routes (P8 and P9, Fig. 10 and Table 12 [142]). The fate of the C(O)OR1 radical is of particular importance as its key pathway (P6P7) leads to either CO or CO2 and determines the extent of the ratio CO2/CO produced, and therefore, the efficiency of the fuel to reduce soot precursor emissions.

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Figure 27. Reaction flux analysis for the oxidation of ethyl butanoate (EB) at 1 atm, 943 K, = 1.1 and for 65% conversion of EB (axial coordinate of the tubular reactor z1/cm = 21). Percentages indicate percent of parent species being converted to daughter species (the continuous arrows correspond to reactive flux the importance of which is shown by arrows of proportional widths while dashed arrows mean a several-step production) [203]. Experimental observations highlighted that the incorporation of oxygenated fuels, including biodiesels, reduces soot production in diesel engines with increased or decreased effectiveness (Section 2.3.2). Indeed, biodiesels do not contain aromatics. Furthermore, Westbrook et al. [246] explained the behavior of oxygenated fuels in fundamental terms. Through a detailed chemical kinetic modeling approach (combining mechanisms for n-heptane as diesel surrogate and for the oxygenated species of interest, MB), the authors attributed these effects to structural characteristics of the oxygenated species, or the ability of each O atom of the fuel molecule to remove one C atom from the product pool of species, which can subsequently generate soot throughout the combustion process. In addition, kinetic modeling located this reduction in concentration of soot precursors in

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the hot products of the fuel-rich diesel ignition zone (between the droplet surface and flame). Whereas soot is usually produced in fuel-rich environments where there is insufficient oxygen for unsaturated hydrocarbon fragments to be completely oxidized (leading them to bond together and produce larger molecules that continue growing until they become soot), the O atoms of the oxygenated fuel promotes the oxidization of these soot precursors at their early stage of formation. These predictions were recently confirmed by experimental studies [101] and [247]. The authors also emphasized the significance of oxygen in biodiesel fuels on soot reduction compared to the oxygen from entrained air. Thus, in the particular case of ester fuels in which two O atoms are initially bonded to single C atoms, the authors noted that when these CO2 moieties result in the direct production of CO2 (directly from the fuel molecule without primary CO oxidation with O2), the efficiency of the oxygenated additives for inhibiting soot formation is ostensibly reduced. Therefore, the desired path for an ideal oxygenated fuel is reaction P6 (as each O atom pairs up with one C atom through CO and OR1 species), while reaction P7 leads to CO2 waste and the soot-reducing potential of the oxygenated fuel (Fig. 26). Accordingly, the lower the CO2/CO ratio that comes directly from the reagent, the more effective the fuel is in reducing soot emissions. Nevertheless, with reference to the CO, (CO)O, and (CO)O bond energy analysis [245,248,249,250] as well as the ab initio estimations [229,233,244] for the branching reaction rates related to the methoxy formyl radical (species C(O)OR1 with R1CH3), reaction pathway P7 leading to CO2 dominates over the reaction pathways leading to CO (P6). This result indicates that ester species may be less effective than ether or alcohol species (where no C atom is bonded to more than one O atom) at reducing soot per oxygen wt% in the fuel. Finally, the overall scheme described in Fig. 26 is consistent with the conclusions proposed by Szybist et al. [186] and [187] for methyl esters and Bennadji et al. [203] for ethyl esters (Fig. 27), according to which decarboxylation of the ester fuel (yielding direct CO2 elimination) likely does not occur until the aliphatic main chain has been largely consumed. Although experiments and kinetic modeling studies have successfully converged to enhance the understanding of CO2 and soot emissions occurring during combustion processes, some refinements may still be produced. For example, the modeling of CO2/CO versus temperature conducted by Herbinet et al. [190] for MD pyrolysis accurately reproduced experiments except at low temperatures (770800 K) and low conversion (0.2%). Over this range of temperatures, the CO2/CO ratio decreased abruptly (with a sudden increase in conversion) and remains constant at higher temperatures. The authors attributed this behavior to wall effects rather than the omission of a unimolecular elimination reaction of CO2 in the proposed detailed mechanism. Nevertheless, Huynh and Violi [229] also computed a decrease in the CO2/CO ratio with temperature using the kinetic modeling of MB pyrolysis. Further experiments and modeling investigations (including large esters) are needed to clarify this behavior and would help in improving combustion mechanism development. In addition, experiments and kinetic modeling studies for pyrolysis/oxidation of n-alkanes and esters of the same sizes, under identical initial conditions, would be very useful for comparing the amounts of CO2 and CO produced from the two classes of fuels in a meaningful way. In addition, they will reinforce similar investigations that were conducted for short methyl ester pyrolysis [173], for n-heptane and MD oxidation [186,187], and for oxidation of a commercial petrodiesel fuel, the corresponding B30 fuel (30% FAME by vol.), and a B30 surrogate (30% MOC in mixture with n-decane and 1-methylnaphtalene) [201]. The results of these investigations will lead to a better understanding of the effectiveness of ester additives in reducing greenhouse gases and pollutant emissions, at least at the combustion stage in engines.

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4.2. Thermochemical properties using ab initio theory and meaningful properties for reliable kinetic model development As shown in previous sections, unsaturated methyl esters and, to a lesser extent, low-molecularweight carbonyls are important intermediate species in the combustion of saturated FAME; however, additional experimental and detailed kinetic studies are required to improve their agreement [189]. Therefore, improved rate parameters and thermochemical data for unsaturated FAME using ab initio theory and corresponding computational methods (selected among those yielding a compromise between accuracy and computational cost) will improve the mechanisms for unsaturated and saturated FAME. More specifically, regarding the oxidation of unsaturated FAME, Westbrook et al. [145] indicated a class of key reactions and a specific interaction that need further attention from both theoretical and direct experimental studies. These are isomerization reactions of RO2 (alkyl and alkyl-ester peroxy radicals) and O2QOOH (alkyl and alkyl-ester hydroperoxy peroxy radicals) (Fig. 4), as well as the degree of interaction of the RO2 group with the embedded C=C double bond(s) in the transition-state ring. As the presence of C=C double bond(s) in the molecule (and in the transition-state ring) is suspected to inhibit RO2 and O2QOOH isomerizations, unbalancing thus the relative contributions of chain-branching and chain-propagation rates in the low-temperature range, it is of particular importance to address this reaction sequences more precisely. In addition, the same authors highlighted that for fuel species with large and complex structures (methyl oleate), there are so many opportunities in kinetic mechanisms for multiple reaction pathways to occur that it is quite possible to produce an accurate prediction of some integrated property (such as an ignition delay time, burning velocity, or overall rate of reaction) and still not describe the complete details of the reaction. This finding is particularly true in the low-temperature regime, where a combination of resonantly stabilized radicals and multiple pathways for large radical isomerization reactions are possible. This makes the choices extremely challenging while their impact is important on the chainbranching and propagation rates of the reaction (Fig. 4), the balance of which must also be correctly predicted. Therefore, the authors suggest placing particular value on the agreement between the overall reactivity and species concentrations than on the integrated properties [145]. 4.3. Kinetics under high-pressure and infinitely dilute conditions The United States Department of Energy (DOE) recently reported that future engine concepts for clean and efficient combustion of the 21st transportation fuels will incorporate ultra-dilute mixtures at pressures considerably higher than those commonly observed in current internal combustion engine technologies. Fuel concentrations as low as 0.1% and ignition pressures as high as 100300 bar (with peak pressures to 500 bar) were reported as being within the conceptual range of practical devices [33]. Dilute mixtures maintain low peak combustion temperatures (and hence pollutant formation rates, such as NOx and soot), while high pressures minimize energy losses during combustion. Nevertheless, under these new operating conditions, the physical and chemical features of the combustion process are likely altered, which induces new challenges for updating experimental techniques used in data simulation and prediction. Kinetic studies under highly dilute, high-pressure conditions are still lacking, although some attempts are beginning to appear in the literature. Ramirez et al. [201] performed an experimental and modeling kinetic study of the oxidation of commercial and surrogate biodiesel fuels (B30) in a JSR at moderate pressures (6 and 10 atm) and dilute conditions (Table 4). The surrogate biodiesel fuel selected was a mixture of n-decane (49%), 1-methyl naphthalene (21%), and MO (30%). The concentration profiles of reactants, stable intermediates, and products as a function of temperature (at fixed residence time) showed that the fuels oxidize similarly, which allowed for the use of the three-component B30 surrogate for kinetic studies. The kinetic modeling study performed using a detailed chemical kinetic model combining the mechanisms previously proposed for each pure component of the B30 surrogate with additional 60

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cross-reactions (Table 5) showed reasonable agreement between the generated JSR data and computations over the entire range of conditions considered. Concerning the effect of the total pressure on the fuel oxidation, analysis of the results obtained at the two pressures investigated (6 and 10 atm) indicated that the importance of the NTC is reduced when total pressure is increased. This result validates the need for further experimental and modeling investigations that will allow progress in understanding oxidation kinetics, particularly under low-temperature and high-pressure conditions. 5. Conclusions Experimental and kinetic modeling studies developed in a symbiotic way have been the core of the dramatic progress made in understanding and controlling the combustion behavior of biodiesels selected as new-generation fuels in diesel engines. To gradually and safely establish the scientific knowledge required as background, the current methodology has been to use mimetic molecules as building blocks, beginning with simple species for pursuing with larger and larger skeletons that are more representative of actual biodiesel fuels (in terms of chemical structure and combustion properties). Thus, MB was first selected to describe the chemical kinetics specific to the ester group under the entire range of engine operating conditions; MD and further surrogate biodiesel fuels (the major FAME components, pure or in mixtures) were targeted to reproduce specific behavior, such as early CO2 formation, NTC phenomena, and the combustion products. Therefore, the progress achieved in the study of biodiesel combustion is a significant contribution to the challenge issued by the DOE [33] aimed at developing alternatives for clean and efficient combustion of 21st century transportation fuels. Nevertheless, one additional requirement that should be accounted for in reaching fully such objectives is to consider potential alternative fuels from cradle to grave in order to increase chance of isolating the candidate(s) that will be sustainable for humans and the environment. Note that one should not expect a unique candidate but rather various potential solutions that hopefully complement each other by playing the role of alternative energy sources to petroleum [38]. Such a global analysis, similar to life cycle assessment (LCA), would help to match the new-generation feedstocks, new production process, new fuel, and compatible engine technology that would lead to the most sustainable alternative (maximizing energy and material efficiency while minimizing environmental and economical impacts). Nevertheless, these changes would require flexibility in the production process (to admit the pertinent raw materials) as in engine technology (to admit various potential fuels). The knowledge base, including the modeling and simulation tools (based on a fully predictive approach), would also need to be extended to predict the physical and chemical behavior of the species involved all along the LCA of the new fuel. Ethyl esters from lipid biomass with high FFA and water contents (such as non-edible oils, WCO or microalgae) and from crude bioethanol using supercritical process (enabling the use of such raw materials) with integrated cogeneration (for improving energy efficiency of the process) would be an example of promising alternatives at the production stage (with the absence of catalyst generating effluents) and at the engine combustion stage (with a fuel generating lower emissions than the commercial methyl biodiesel). The HCCI strategy has proven to be a successful fuel-flexible engine technology that combines ultra-dilute combustion and LTC (generating low NOx emissions), well-mixed fuel and air streams (avoiding soot formation), and high efficiency (by operating under high pressures). Thus, the technology for achieving this potential alternative from the production process to the engine is already available in principle (except for microalgae still requiring additional research). However, efforts will need to be focused on the development of models, integrating both kinetic phenomena and phase equilibria thermodynamics, which are necessary to simulate the production process and engine combustion under high pressures, moderate temperatures, and dilute medium. Regarding the kinetics of FAEE oxidation, research efforts in the area of experimental and 61

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chemical kinetic modeling will need to be pursued intensively because the oxidation of FAEE proceeds through FFA as intermediates. Therefore, the oxidation chemical kinetics of large carboxylic acids would need to be deepened or even extended (beyond nonanoic acid). As example for the HCCI engine, this step is particularly important because the performance of the engine depends highly on the nature of the fuel, through its capacity to form homogeneous mixtures with air and its ignition timing controlled by in-cylinder chemistry. Nevertheless, as highlighted by Westbrook et al. [145] for methyl ester-based biodiesel fuels, rapid progress can be made in a challenging subject area regardless of whether many researchers collectively focus their attention on it. Therefore, the transfer of knowledge and technology from FAME- to FAEE-based biodiesel fuels should be made rapidly. Acknowledgments The authors would like to sincerely thank the corresponding authors who agreed to send the original figures of their publication(s) referenced in the present manuscript. Acronyms and abbreviations
ASTM: American Society of Testing and Materials BSFC: brake specific fuel consumption BXX: blend of XX% biodiesel fuel and (100 XX)% petrodiesel fuel by volume CAD: crank angle degree CFD: computational fluid dynamics CFNPF: coflowing laminar non-premixed flame CFR: Cooperative-Fuel Research CN: cetane number CR: compression ratio DG: diglycerides DOE: Department of Energy Ea: activation energy (cal) EB: ethyl butanoate EHN: 2-ethylhexylnitrate EHX: ethyl hexanoate EN: ethyl nonane EP: ethyl propanoate FAEE: fatty acid ethyl esters FAME: fatty acid methyl esters FFA: free fatty acids FID: flame ionization detector FR: flow reactor FTIR: Fourier transformed-infrared GC-DET: gas chromatography coupled with a DET detector with DET = MS, FID, or TCD. HCCI: homogeneous-charge compression-ignition HRR: heat release rate HTHR: high-temperature heat release ID: ignition delay iPrAc: isopropyl acetate JSR: jet-stirred reactor k: rate constant expressed by the modified Arrhenius equation as k(T) = ATnexp(Ea/RT) with units of mol, cm, s, cal, and K. Kc: equilibrium constant based on concentration KOEE: Karanja oil ethyl esters KOME: Karanja oil methyl esters kreverse(forward): rate constant for the reverse (forward) reaction LTC: low-temperature combustion LTHR: low-temperature heat release MB: methyl butanoate MC: methyl crotonate MD: methyl decanoate MD5EN: methyl-5 decanoate

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MD9EN: methyl-9 decanoate MDO: methyl dodecanoate MG: monoglycerides MH: methyl heptanoate MHX: methyl hexanoate MiBu: methyl isobutyrate MLO: methyl linoleate MLN: methyl linolenate MM: methyl myristate MN: methyl nonane MN2EN: methyl-2 nonenoate MN3EN: methyl-3-nonenoate MO: methyl oleate MOC: methyl octanoate MOEE: Mahua oil ethyl esters MP: methyl palmitate MS: mass spectroscopy MST: methyl stearate nC16: n-hexadecane nC7: n-heptane NOx: nitrogen oxides NTC: negative temperature coefficient OFDF: opposed-flow diffusion flame P: pressure (atm) PAH: polyaromatic hydrocarbons PFR: plug-flow reactor PM: particulate matter PrAc: propyl acetate PSR: perfectly stirred (tank) reactor Q: volumetric flow rate R: ideal gas constant RCM: rapid compression machine REE: rapeseed oil ethyl esters RME: rapeseed oil methyl esters SME: soybean oil methyl esters SOx: sulfur oxides SP: species profile ST: shock tube T: temperature (K) TCD: thermal conductivity detector TG: triglycerides THC: total hydrocarbons UHC: unburned hydrocarbons V: volume (of reactor, cylinder, etc.) VOC: volatile organic compounds VPFR: variable pressure-flow reactor WCOEE: waste cooking oil ethyl esters (from vegetable oils and animal fats) WCOME: waste cooking oil methyl esters (from vegetable oils and animal fats) WVOEE: waste vegetable oil ethyl esters xfuel: fuel molar fraction xO2: oxygen molar fraction fuel: stoichiometric coefficient of the fuel O2: stoichiometric coefficient of the oxygen : equivalence ratios; for example, =(xfuel/xO2)/(fuel/O2) for reaction CnHm + (n + m/4)O2 nCO2 + m/2 H2O with fuel = 1 and O2=(n+m/4) : residence time = V/Q th iG: i -generation of biofuels (1G, 2G, and 3G for the first-, second-, and third-generation biofuels, respectively)

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References
[1] Y. Zhang, Y. Yang, A.L. Boehman, Premixed ignition behavior of C9 fatty acid esters: a motored engine study, Combustion and Flame, 156 (2009), pp. 12021213 [2] International Energy Outlook 2011, Office of communications, EI-40U.S. Energy Information Administration, Forrestal Building, Washington, DC 20585 (2011) DOE/EIA-0484 [3]J.C. Escobar, E.S. Lora, O.J. Venturini, E.E. Yanez, E.F. Castillo, O. Almazan, Biofuels: environment, technology and food security, Renewable and Sustainable Energy Reviews, 13 (2009), pp. 12751287 [4]P.N. Nigam, A. Singh, Production of liquid biofuels from renewable resources, Progress in Energy and Combustion Science, 37 (2011), pp. 5268 [5] A.K. Agarwal, Biofuels (alcohols and biodiesel) applications as fuels for internal combustion engines, Progress in Energy and Combustion Science, 33 (2007), pp. 233271 [6] A. Demirbas, Progress and recent trends in biofuels, Progress in Energy and Combustion Science, 33 (2007), pp. 118 [7] A.K. Hossain, P.A. Davies, Plant oils as fuels for compression-ignition engines: a technical review and life-cycle analysis, Renewable Energy, 35 (2010), pp. 113

hal-00846052, version 1 - 18 Jul 2013

[8] A. Murugesan, C. Umarami, R. Subramanian, N. Nedunchezhian, Bio-diesel as an alternative fuel for diesel engines a review, Renewable and Sustainable Energy Reviews, 13 (2009), pp. 653662 [9] M.S. Graboski, R.L. McCormick, Combustion of fat and vegetable oil derived fuels in diesel engines, Progress in Energy and Combustion Science, 24 (1998), pp. 125164 [10] M. Lapuerta, O. Armas, J. Rodriguez-Fernandez, Effect of biodiesel fuels on diesel engine emissions, Progress in Energy and Combustion Science, 34 (2008), pp. 198223 [11] J.Q.A. Brito, C.S. Silva, J.S. Almeida, M.G.A. Korn, Mauro Korn, L.S.G. Teixeira, Ultrasound-assisted synthesis of ethyl esters from soybean oil via homogeneous catalysis, Fuel Processing Technology, 95 (2012), pp. 3336 [12] C. Brunschwig, W. Moussavou, J. Blin, Use of bioethanol for biodiesel production, Progress in Energy and Combustion Science, 38 (2012), pp. 283301 [13] E. Lois, Definition of biodiesel, Fuel, 86 (2007), pp. 12121213 [14] H. Haberl, T. Beringer, S.C. Bhattacharya, K.H. Erb, M. Hoogwijk, The global technical potential of bio-energy in 2050 considering sustainability constraints, Current Option in Environmental Sustainability, 2 (2010), pp. 394403 [15] L. Reijnders, The life cycle emission of greenhouse gases associated with plants oils used as biofuels, Renewable Energy, 36 (2011), pp. 879880 [16] Y.C. Sharma, B. Singh, S.N. Upadhyay, Advancements in development and characterization of biodiesel: a review, Fuel, 87 (2008), pp. 23552373 [17] J. Janaun, N. Ellis, Perspectives on biodiesel as a sustainable fuel, Renewable and Sustainable Energy Reviews, 14 (2010), pp. 13121320 [18] A. Karmakar, S. Kamakar, S. Mukherjee, Properties of various plants and animals feedstocks for biodiesel production, Bioresource Technology, 101 (2010), pp. 72017210 [19] R.C. Saxena, D.K. Adhikari, H.B. Goyal, Biomass-based energy fuel through biochemical routes: a review, Renewable and Sustainable Energy Reviews, 13 (2009), pp. 167178 [20] L.F. Gutirrez, O.J. Snchez, C.A. Cardona, Process integration possibilities for biodiesel production from palm oil using ethanol obtained from lignocellulosic residues of oil palm industry, Bioresource Technology, 100 (2009), pp. 12271237 [21] J.C. Juan, D.A. Kartika, T.Y. Wu, T.Y. Yun Hin, Biodiesel production from Jatropha oil by catalytic and non-catalytic approach: an overview, Bioresource Technology, 102 (2011), pp. 452460

64

[22] Y.C. Sharma, B. Singh, A hybrid feedstock for a very efficient preparation of biodiesel, Fuel Processing Technology, 91 (2010), pp. 12671273 [23] A. Karmakar, S. Karmakar, S. Mukherjee, Biodiesel production from neem towards feedstock diversification: Indian perspective, Renewable and Sustainable Energy Reviews, 16 (2012), pp. 10501060 [24] M.G. Kulkarni, A.K. Dalai, Waste cooking oil an economical source for biodiesel: a review, Industrial & Engineering Chemistry Research, 45 (2006), pp. 29012913 [25] A.B. Chhetri, K.C. Watts, M.R. Islam, Waste cooking oil as an alternate feedstock for biodiesel production, Energies, 1 (2008), pp. 313 [26] V.F. Marulanda, G. Anitescu, L.L. Tavlarides, Biodiesel fuels through a continuous flow process of chicken fat supercritical transesterification, Energy & Fuels, 24 (2010), pp. 253260 [27] R. Behet, Performance and emission study of waste anchovy fish biodiesel in diesel engine, Fuel Processing Technology, 92 (2011), pp. 11871194 [28] X. Zeng, M.K. Danquah, X.D. Chen, Y. Lu, Microalgae bioengineering: from CO2 fixation to biofuels production, Renewable and Sustainable Energy Reviews, 15 (2011), pp. 32523260 [29] X. Liu, A.F. Clarens, L.M. Colosi, Algae biodiesel has potential despite inconclusive results to date, Bioresource Technology, 104 (2012), pp. 803806 [30] M.J. Ramos, C.M. Fernndez, A. Casas, L. Rodrguez, . Prez, Influence of fatty acid composition of raw materials on biodiesel properties, Bioresource Technology, 100 (2009), pp. 261268 [31] M.F. Demirbas, M. Balat, H. Balat, Biowastes-to-biofuels, Energy Conversion and Management, 52 (2011), pp. 1815 1828 [32] M.J. Groom, E.M. Gray, P.A. Townsend, Biofuels and biodiversity: principles for creating better policies for biofuels production, Conservation Biology, 22 (2008), pp. 602609 [33] A. Mcllroy, G. McRae, V. Sick, D.L. Siebers, C.K. Westbrook, P.J. Smith et al., Basic research needs for clean and efficient combustion of 21st century transportation fuels, http://science.energy.gov//media/bes/pdf/reports/files/ctf_rpt.pdf (2006) [34] K. Kohse-Hinghaus, P. Osswald, T.A. Cool, T. Kasper, N. Hansen, F. Qi et al., Biofuel combustion chemistry: from ethanol to biodiesel, Angewandte Chemie International Edition, 49 (2010), pp. 35723597 [35] J.Y.W. Lai, K.C. Lin, A. Violi, Biodiesel combustion: advances in chemical kinetic modelling, Progress in Energy and Combustion Science, 37 (2011), pp. 114 [36] I.M. Atadashi, M.K. Aroua, A.A. Aziz, High quality biodiesel and its diesel engine application: a review, Renewable and Sustainable Energy Reviews, 14 (2010), pp. 19992008 [37] G. Anitescu, T.J. Bruno, Fluid properties needed in supercritical transesterification of triglyceride feedstocks to biodiesel fuels for efficient and clean combustion a review, The Journal of Supercritical Fluids, 63 (2012), pp. 133149 [38] G. Knothe, Biodiesel and renewable diesel: a comparison, Progress in Energy and Combustion Science, 36 (2010), pp. 364373 [39] Y.C. Sharma, B. Singh, Development of biodiesel: current scenario, Renewable and Sustainable Energy Reviews, 13 (2009), pp. 16461651 [40] A.P.S. Chouhan, A.K. Sarma, Modern heterogeneous catalysts for biodiesel production: a comprehensive review, Renewable and Sustainable Energy Reviews, 15 (2011), pp. 43784399 [41] E.M. Shahid, Y. Jamal, Production of biodiesel: a technical review, Renewable and Sustainable Energy Reviews, 15 (2011), pp. 47324745 [42] J. Van Gerpen, Biodiesel processing and production, Fuel Processing Technology, 86 (2005), pp. 10971107

hal-00846052, version 1 - 18 Jul 2013

65

[43] Y. Zhang, M.A. Dub, D.D. McLean, M. Kates, Biodiesel production from waste cooking oil: 1. Process design and technological assessment, Bioresource Technology, 89 (2003), pp. 116 [44] S. Furuta, H. Matsuhashi, K. Arata, Biodiesel fuel production with solid superacid catalysis in fixed bed reactor under atmospheric pressure, Catalysis Communication, 5 (2004), pp. 721723 [45] A. Demirbas, Biodiesel fuels from vegetable oils via catalytic and non-catalytic supercritical alcohol transesterifications and other methods: a survey, Energy Conversion and Management, 44 (2003), pp. 20932109 [46] V. Rathore, G. Madras, Synthesis of biodiesel from edible and non-edible oils in supercritical alcohols and enzymatic synthesis in supercritical carbon dioxide, Fuel, 86 (2007), pp. 26502659 [47] M.E. Borges, L. Daz, Recent development on heterogeneous catalysts for biodiesel production by oil esterification and transesterification reactions: a review, Renewable and Sustainable Energy Reviews, 16 (2012), pp. 28392849 [48] L. Bournay, D. Casanave, B. Delfort, G. Hillion, J.A. Chodorge, New heterogeneous process for biodiesel production: a way to improve the quality and the value of the crude glycerin produced by biodiesel plants, Catalysis Today, 106 (2005), pp. 190192 [49] B. Salamatinia, A.Z. Abdullah, S. Bhatia, Quality evaluation of biodiesel produced through ultrasound-assisted heterogeneous catalytic system, Fuel Processing Technology, 97 (2012), pp. 18

hal-00846052, version 1 - 18 Jul 2013

[50] A.M. Dehkordi, M. Ghasemi, Transesterification of waste cooking oil to biodiesel using Ca and Zr mixed oxides as heterogeneous base catalysts, Fuel Processing Technology, 97 (2012), pp. 4551 [51] O. Ilgen, Reaction kinetics of dolomite catalyzed transesterification of canola oil and methanol, Fuel Processing Technology, 95 (2012), pp. 6266 [52] H. Noureddini, X. Gao, R.S. Philkana, Immobilized Pseudomonas cepacia lipase for biodiesel fuel production from soybean oil, Bioresource Technology, 96 (2005), pp. 769777 [53] J.M. Marchetti, V.U. Miguel, A.F. Errazu, Possible methods for biodiesel production, Renewable and Sustainable Energy Reviews, 11 (2007), pp. 13001311 [54] M.G. Jang, D.K. Kim, S.C. Park, J.S. Lee, S.W. Kim, Biodiesel production from crude canola oil by two-step enzymatic processes, Renewable Energy, 42 (2012), pp. 99104 [55] J.M.N. van Kasteren, A.P. Nisworo, A process model to estimate the cost of industrial scale biodiesel production from waste cooking oil by supercritical transesterification, Resources, Conservation and Recycling, 50 (2007), pp. 442458 [56] H.V. Lee, R. Yunus, J.C. Juan, Y.H. Taufiq-Yap, Process optimization design for Jatropha-based biodiesel production using response surface methodology, Fuel Processing Technology, 92 (2011), pp. 24202428 [57] H. Noureddini, D. Zhu, Kinetics of transesterification of soybean oil, Journal of the American Oil Chemists' Society, 74 (1997), pp. 14571463 [58] E. Lotero, Y. Liu, D.E. Lopez, K. Suwannakarn, D.A. Bruce, J.G. Goddwin, Synthesis of biodiesel via acid catalysis, Industrial & Engineering Chemistry Research, 44 (2005), pp. 53535363 [59] D.R. Mendona, H.M.C. Andrade, P.R.B. Guimaraes, R.F. Vianna, S.M.P. Meneghetti, L.A.M. Pontes et al., Application of full factorial design and Doehlert matrix for the optimization of beef tallow methanolysis via homogeneous catalysis, Fuel Processing Technology, 3 (2011), pp. 342348 [60] M. Charoenchaitrakool, J. Thienmethangkoon, Statistical optimization for biodiesel production from waste frying oil through two-step catalyzed process, Fuel Processing Technology, 92 (2011), pp. 112118 [61] G.F. Silva, F.L. Camargo, A.L.O. Ferreira, Application of response surface methodology for optimization of biodiesel production by transesterification of soybean oil with ethanol, Fuel Processing Technology, 92 (2011), pp. 407413 [62] W. Zhou, D.G.B. Boocock, Phase behavior of the base-catalyzed transesterification of soybean oil, Journal of the American Oil Chemists' Society, 82 (2006), pp. 10471052

66

[63] W. Zhou, D.G.B. Boocock, Phase distributions of alcohol, glycerol, and catalyst in the transesterification of soybean oil, Journal of the American Oil Chemists' Society, 83 (2006), pp. 10411045 [64] J.M. Encinar, J.F. Gonzalez, A. Rodriguez-Reinares, Biodiesel from used frying oil. Variables affecting the yields and characteristics of the biodiesel, Industrial & Engineering Chemistry Research, 44 (2005), pp. 54915499 [65] T. Issariyakul, M.G. Kulkarni, A.K. Dalai, N.N. Bakhshi, Production of biodiesel from waste fryer grease using mixed methanol/ethanol system, Fuel Processing Technology, 88 (2007), pp. 429436 [66] J.M. Encinar, J.F. Gonzales, A. Rodriguez-Reinares, Ethanolysis of used frying oil. Biodiesel preparation and characterization, Fuel Processing Technology, 28 (2007), pp. 513522 [67] T. Issariyakul, M.G. Kulkarni, L.C. Meher, A.K. Dalai, N.N. Bakhshi, Biodiesel production from mixtures of canola oil and used cooking oil, Chemical Engineering Journal, 140 (2008), pp. 7785 [68] R. Fillires, B. Benjelloun-Mlayah, M. Delmas, Ethanolysis of rapeseed oil: quantification of ethyl esters, mono-, di-, and triglycerides and glycerol by high performance size-exclusion chromatography, Journal of the American Oil Chemists' Society, 72 (1995), pp. 427432 [69] O.S. Stamenkovi, A.V. Velikovi, V.B. Veljkovi, The production of biodiesel from vegetable oils by ethanolysis: current state and perspectives, Fuel, 90 (2011), pp. 31413155

hal-00846052, version 1 - 18 Jul 2013

[70] E. Alptekin, M. Canakci, Optimization of pretreatment reaction for methyl ester production from chicken fat, Fuel, 89 (2010), pp. 40354039 [71] S. Saka, D. Kusdiana, Biodiesel fuel from rapeseed oil as prepared in supercritical methanol, Fuel, 80 (2001), pp. 225 231 [72] Y. Warabi, D. Kusdiana, S. Saka, Reactivity of triglycerides and fatty acids of rapeseed oil in supercritical alcohols, Bioresource Technology, 91 (2004), pp. 283287 [73] Y. Isayama, S. Saka, Biodiesel production by supercritical process with crude bio-methanol prepared by wood gasification, Bioresource Technology, 99 (2008), pp. 47754779 [74] K.T. Tan, M.M. Gui, K.T. Lee, A.R. Mohamed, An optimized study of methanol and ethanol in supercritical alcohol technology for biodiesel production, The Journal of Supercritical Fluids, 53 (2010), pp. 8287 [75] H.Y. Shin, S.M. Lim, S.C. Kang, S.Y. Bae, Statistical optimization for biodiesel production from rapeseed oil via transesterification in supercritical methanol, Fuel Processing Technology, 98 (2012), pp. 15 [76] D. Kusdiana, S. Saka, Effects of water on biodiesel fuel production by supercritical fuel production by supercritical methanol treatment, Bioresource Technology, 91 (2004), pp. 289295 [77] A. Murugesan, C. Umarani, T.R. Chinnusamy, M. Krishnan, R. Subramanian, N. Neduzchezhain, Production and analysis of bio-diesel from non-edible oils a review, Renewable and Sustainable Energy Reviews, 13 (2009), pp. 825834 [78] Assmann G, Blas G, Gutsche B, Jeromin L, Rigal J, Armengaud R, et al. World Patent WO 91 05, o34; 1991. [79] M.C. Manique, C.S. Faccini, B. Onorevoli, E.V. Benvenutti, E.B. Caramo, Rice husk ash as an adsorbent for purifying biodiesel from waste frying oil, Fuel, 92 (2012), pp. 5661 [80] M. Canaki, J. van Gerpen, A pilot plant to produce biodiesel from high free fatty acid feedstock, Transactions of the ASABE, 46 (2003), pp. 945954 [81] M.L. Pisarello, B. Dalla Costa, G. Mendow, C.A. Querini, Esterification with ethanol to produce biodiesel from high acidity raw materials kinetic studies and analysis of secondary reactions, Fuel Processing Technology, 91 (2010), pp. 1005 1014 [82] S. Jansri, S.B. Ratanawilai, M.L. Allen, G. Prateepchaikul, Kinetics of methyl ester production from mixed crude palm oil by using acid-alkali catalyst, Fuel Processing Technology, 92 (2011), pp. 15431548 [83] A. Dhar, R. Kevin, A.K. Agarwal, Production of biodiesel from high-FFA neem oil and its performance, emission and combustion characterization in a single cylinder DICI engine, Fuel Processing Technology, 97 (2012), pp. 118129

67

[84] I. Vieitez, C. da Silva, G.R. Borges, F.C. Corazza, J.V. Oliveira, M.A. Grompone et al., Continuous production of soybean biodiesel in supercritical ethanol water mixtures, Energy & Fuels, 22 (2008), pp. 28052809 [85] I. Vieitez, C. da Silva, I. Alckmin, G.R. Borges, F.C. Corazza, J.V. Oliveira et al., Continuous catalyst-free methanolysis and ethanolysis of soybean oil under supercritical alcohol/water mixtures, Renewable Energy, 35 (2010), pp. 19761981 [86] I. Vieitez, M.J. Pardo, C. da Silva, C. Bertoldi, F. de Castilhos, J.V. Oliveira et al., Continuous synthesis of castor oil ethyl esters under supercritical ethanol, The Journal of Supercritical Fluids, 56 (2011), pp. 271276 [87] C. Bertoldi, C. da Silva, J.P. Bernardon, M.L. Corazza, L.C. Filho, J.V. Oliveira et al., Continuous production of biodiesel from soybean oil in supercritical ethanol and carbon dioxide as cosolvent, Energy & Fuels, 23 (2009), pp. 51655172 [88] C.M. Trentin, A.P. Lima, I.P. Alkimim, C. da Silva, F. de Castilhos, Continuous production of soybean biodiesel with compressed ethanol in a microtube reactor using carbon dioxide as co-solvent, Fuel Processing Technology, 92 (2011), pp. 952958 [89] V. Patil, K.Q. Tran, H.R. Giselrod, Towards sustainable production of biofuels from microalgae, International Journal of Molecular Sciences, 9 (2008), pp. 11881195 [90] G. Anitescu, A. Deshpande, L.L. Tavlarides, Integrated technology for supercritical biodiesel production and power cogeneration, Energy & Fuels, 22 (2008), pp. 13911399

hal-00846052, version 1 - 18 Jul 2013

[91] F. Jin, X. Zeng, J. Cao, K. Kawasaki, A. Kishita, K. Tohji et al., Partial hydrothermal oxidation of unsaturated high molecular weight carboxylic acids for enhancing the cold flow properties of biodiesel fuel, Fuel, 89 (2010), pp. 24482454 [92] R.B. Levine, T. Pinnarat, P.E. Savage, Biodiesel production from wet algal biomass through in situ lipid hydrolysis and supercritical transesterification, Energy & Fuels, 24 (2010), pp. 52355243 [93] A. Santana, J. Maaira, M.A. Larrayoz, Continuous production of biodiesel from vegetable oil using supercritical ethanol/carbon dioxide mixtures, Fuel Processing Technology, 96 (2012), pp. 214219 [94] M. Ayoub, A.Z. Abdullah, Critical review on the current scenario and significance of crude glycerol resulting from biodiesel industry towards more sustainable renewable energy industry, Renewable and Sustainable Energy Reviews, 16 (2012), pp. 26712686 [95] J.F. Izquierdo, M. Montiel, I. Pals, P.R. Outn, M. Galn, L. Jutglar et al., Fuel additives from glycerol etherification with light olefins: state of the art, Renewable and Sustainable Energy Reviews, 16 (2012), pp. 67176724 [96] F.J.G. Ortiz, P. Ollero, A. Serrera, S. Galera, An energy and exergy analysis of the supercritical water reforming of glycerol for power production, International Journal of Hydrogen Energy, 37 (2012), pp. 209226 [97] C. Varrone, B. Giussani, G. Izzo, G. Massini, A. Marone, A. Signorini et al., Statistical optimization of biohydrogen and ethanol production from crude glycerol by microbial mixed culture, International Journal of Hydrogen Energy, 37 (2012), pp. 1647916488 [98] A.E. Atabani, A.S. Silitonga, I.A. Badruddin, T.M.I. Mahlia, H.H. Masjuki, S. Mekhilef, A comprehensive review on biodiesel as an alternative energy resource and its characteristics, Renewable and Sustainable Energy Reviews, 16 (2012), pp. 20702093 [99] S. Jain, M.P. Sharma, Stability of biodiesel and its blends: a review, Renewable and Sustainable Energy Reviews, 14 (2010), pp. 667678 [100] M.R. Monteiro, A.R.P. Ambrozin, L.M. Liao, A.G. Ferreira, Critical review on analytical methods for biodiesel characterization, Talanta, 77 (2008), pp. 593605 [101] X. Wang, Z. Huang, O.A. Kuti, W. Zhang, K. Nishida, An experimental investigation on spray, ignition and combustion characteristics of biodiesels, Proceedings of the Combustion Institute, 33 (2011), pp. 20712077 [102] K. Wadumesthrige, M. Ara, S.O. Salley, K.Y.S. Ng, Investigation of lubricity characteristics of biodiesel in petroleum and synthetic fuel, Energy & Fuels, 23 (2009), pp. 22292234

68

[103] A. Dubreuil, F. Foucher, C. Mounam-Rousselle, G. Dayma, P. Dagaut, HCCI combustion: effect of NO in EGR, Proceedings of the Combustion Institute, 31 (2007), pp. 28792886 [104] B. Freedman, M.O. Bagby, T.J. Callahan, T.W. Ryan, Cetane numbers of fatty esters, fatty alcohols, and triglycerides determined in a constant volume combustion bomb. SAE Paper no. 900343, International Congress & Exposition, February 1990, United States, Detroit, Michigan (1990) http://papers.sae.org/900343/ [105] G. Knothe, A.C. Matheaus, T.W. Ryan III, Cetane numbers of branched and straight chain fatty esters determined in an ignition quality tester, Fuel, 82 (2003), pp. 971975 [106] C.Y. May, Y.C. Liang, C.S. Foon, M.A. Ngan, C.C. Hook, Y. Basiron, Key fuel properties of palm oil alkyl esters, Fuel, 84 (2005), pp. 17171720 [107] S.A. Basha, K.R. Gopal, S. Jebaraj, A review on biodiesel production, combustion, emissions and performance, Renewable and Sustainable Energy Reviews, 13 (2009), pp. 16281634 [108] J. Krahl, G. Knothe, A. Munack, Y. Ruschel, O. Schrder, E. Hallier et al., Comparison of exhaust emissions and their mutagenicity from the combustion of biodiesel, vegetable oil, gas-to-liquid and petrodiesel fuels, Fuel, 88 (2009), pp. 1064 1069 [109] R. Lee, C.H. Hobbs, J.F. Pedley, A fuel quality impact on heavy duty diesel emissions: a literature review. SAE paper no. 982649, International Fall Fuels and Lubricants Meeting and Exposition, October 1998, United States, San Francisco, California (1998) http://papers.sae.org/982649/ [110] N. Ladommatos, M. Parsi, A. Knowles, The effect of fuel cetane improve on diesel pollutant emissions, Fuel, 75 (1996), pp. 814 [111] M.E. Tat, Cetane number effect on the energetic and exergetic efficiency of a diesel engine fuelled with biodiesel, Fuel Processing Technology, 92 (2011), pp. 13111321 [112] C.L. Peterson, D.L. Reece, J.C. Thompson, S.M. Beck, C. Chases, Ethyl ester of rapeseed used as a biodiesel fuel a case study, Biomass Bioenergy, 10 (1996), pp. 331336 [113] G. Karavalakis, G. Fontara, D. Ampatzoglou, M. Kousoulidou, S. Stournas, Z. Samaras et al., Effects of low concentration biodiesel blends application on modern passenger cars. Part 3. Impact on PAH, nitro-PAH, and oxy-PAH emissions, Environmental Pollution, 157 (2010), pp. 15841594 [114] G. Fontaras, G. Karavalakis, M. Kousoulidou, L. Ntziachristos, E. Bakeas, S. Stournas et al., Effects of low concentration biodiesel blend application on modern passenger cars. Part 1. Feedstock impact on regulated pollutants, fuel consumption and particle emissions, Environmental Pollution, 158 (2010), pp. 14511460 [115] G. Fontaras, G. Karavalakis, M. Kousoulidou, L. Ntziachristos, E. Bakeas, S. Stournas et al., Effects of low concentration biodiesel blend application on modern passenger cars. Part 2. Impact on carbonyl compound emissions, Environmental Pollution, 158 (2010), pp. 24962503 [116] L. Serrano, V. Carreira, R. Cmara, M. Gameiro da Silva, On-road performance comparison of two identical cars consuming petrodiesel and biodiesel, Fuel Processing Technology, 103 (2012), pp. 125133 [117] C.C. Enweremadu, H.L. Rutto, Combustion, emission and engine performance characteristics of used cooking oil biodiesel a review, Renewable and Sustainable Energy Reviews, 14 (2010), pp. 28632873 [118] Pillot D, Besombes J-L, Cazier F, Hanoune B, Combet E, Delbende A, et al. Exhaust emissions from light vehicles fuelled with different biofuels. In: 17th conference Transport and air pollution, ETTAP; 2009. [119] K. Muralidharan, D. Vasudevan, Performance, emission and combustion characteristics of a variable compression ratio engine using methyl esters of waste cooking oil and diesel blends, Applied Energy, 88 (2011), pp. 39593968 [120] A.N. Ozsezen, M. Canakci, Determination of performance and combustion characteristics of a diesel engine fueled with canola and waste palm oil methyl esters, Energy Conversion and Management, 52 (2011), pp. 108116 [121] C.J. Mueller, A.L. Boehman, G.C. Martin, An experimental investigation on the origin of increased NOx emissions when fuelling a heavy-duty compression-ignition engine with soy biodiesel, SAE International Journal of Fuels and Lubricants, 2 (October 2009), pp. 789816 http://dx.doi.org.bases-doc.univ-lorraine.fr/10.4271/2009-01-1792

hal-00846052, version 1 - 18 Jul 2013

69

[122] B. Baiju, M.K. Naik, L.M. Das, A comparative evaluation of compression ignition engine characteristics using methyl and ethyl esters of Karanja oil, Renewable Energy, 34 (2009), pp. 16161621 [123] M. Lapuerta, J.M. Herreros, L.L. Lyons, R. Gara-Contreras, Y. Briceo, Effect of the alcohol type used in the production of waste cooking oil biodiesel on diesel performance and emissions, Fuel, 87 (2008), pp. 31613169 [124] Z. Utlu, M.S. Koak, The effect of biodiesel fuel obtained from waste frying oil on direct injection diesel engine performance and exhaust emissions, Renewable Energy, 33 (2008), pp. 19361941 [125] S.K. Hoekman, C. Robbins, Review of the effects of biodiesel on NOx emissions, Fuel Processing Technology, 96 (2012), pp. 237249 [126] T. Fang, C.F. Lee, Biodiesel effects on combustion processes in an HSDI diesel engine using advanced injection strategies, Proceedings of the Combustion Institute, 32 (2009), pp. 27852792 [127] W. Yuan, A.C. Hansen, Computational investigation of the effect of biodiesel fuel properties on diesel engine NOx emissions, International Journal of Agricultural and Biological Engineering, 2 (2009), pp. 4148 [128] J. Huang, L. Lin, Y. Wang, J. Qin, A.P. Roskilly, L. Li et al., Experimental study of the performance and emission characteristics of diesel engine using direct and indirect injection systems and different fuels, Fuel Processing Technology, 92 (2011), pp. 13801386

hal-00846052, version 1 - 18 Jul 2013

[129] A. Schnborn, N. Ladommatos, J. Williams, R. Allan, J. Rogerson, The influence of molecular structure of fatty acid monoalkyl esters on diesel combustion, Combustion and Flame, 156 (2009), pp. 13961412 [130] R.L. McCormick, M.S. Graboski, T.L. Alleman, A.M. Herring, Impact of biodiesel source material and chemical structure on emissions of criteria pollutants from a heavy-duty engine, Environmental Science & Technology, 35 (2001), pp. 1742 1747 [131] H. Jung, D. Kittelson, M. Zachariah, Characteristic of SME biodiesel-fueled diesel particle emissions and the kinetics of oxidation, Environmental Science & Technology, 40 (2006), pp. 49494955 [132] A. Tsolakis, Effect on particle size distribution from the diesel engine operating on RME-biodiesel with EGR, Energy & Fuels, 20 (2006), pp. 14181424 [133] A. Flgel, M. Milchev, J. Kiefer, A. Leipertz, Characterization of soot emission from diesel and biodiesel laminar diffusion flames by laser-induced incandescence (LII), Proceedings of the fifth European combustion meeting, Cardiff University (28 June1 July 2011) [134] S. Bejaoui, R. Lemaire, E. Therssen, Pascale Desgroux, Study of the effect of rapeseed methyl ester addition in diesel fuel on soot formation, Proceedings of the fifth European combustion meeting, Cardiff University (28 June1 July 2011) [135] C. He, Y. Ge, J. Tan, K. You, X. Han, J. Wang et al., Comparison of carbonyl compounds emissions from diesel engine fueled with biodiesel and diesel, Atmospheric Environment, 43 (2009), pp. 36573661 [136] V. Makareviciene, P. Janulis, Environmental effect of rapeseed oil ethyl ester, Renewable Energy, 28 (2003), pp. 2395 2403 [137] M. Al-Widyan, G. Tashtoush, M. Abu-Qudais, Utilization of ethyl ester of waste vegetable oils as fuel in diesel engines, Fuel Processing Technology, 76 (2002), pp. 91103 [138] S. Puhana, N. Vedaramana, G. Sankaranarayanana, B.V. Bharat Rama, Performance and emission study of Mahua oil (madhuca indica oil) ethyl ester in a 4-stroke natural aspirated direct injection diesel engine, Renewable Energy, 30 (2005), pp. 12691278 [139] C.L. Peterson, D.L. Reece, R. Cruz, J. Thompson, A comparison of ethyl and methyl esters of vegetable oil as diesel fuel substitutes, liquid fuels from renewable resources, Proceedings of an alternative energy conference, ASAE, St Joseph, MI 49085-9659 (1992) [140] J.M. Simmie, Detailed chemical kinetic models for the combustion of hydrocarbons fuel, Progress in Energy and Combustion Science, 29 (2003), pp. 599634

70

[141] F. Battin-Leclerc, Detailed chemical kinetic models for the low-temperature combustion of hydrocarbons with application to gasoline and diesel fuel surrogates, Progress in Energy and Combustion Science, 34 (2008), pp. 440498 [142] O. Herbinet, W.J. Pitz, C.K. Westbrook, Detailed chemical kinetic oxidation mechanism for a biodiesel surrogate, Combustion and Flame, 154 (2008), pp. 507528 [143] O. Herbinet, W.J. Pitz, C.K. Westbrook, Detailed chemical kinetic mechanism for the oxidation of biodiesel fuels blend surrogate, Combustion and Flame, 157 (2010), pp. 893908 [144] C.V. Naik, C.K. Westbrook, O. Herbinet, W.J. Pitz, M. Mehl, Detailed chemical kinetic reaction mechanism for biodiesel components methyl stearate and methyl oleate, Proceedings of the Combustion Institute, 33 (2011), pp. 383389 [145] C.K. Westbrook, C.V. Naik, O. Herbinet, W.J. Pitz, M. Mehl, S.M. Sarathy et al., Detailed chemical kinetic reaction mechanism for soy and rapeseed biodiesel fuels, Combustion and Flame, 158 (2011), pp. 742755 [146] R. Grana, A. Frassoldati, A. Cuoci, T. Faravelli, E. Ranzi, A wide range kinetic modeling study of pyrolysis and oxidation of methyl butanoate and methyl decanoate. Note I: Lumped kinetic model of methyl butanoate and small methyl esters, Energy, 43 (2012), pp. 124139 [147] R. Grana, A. Frassoldati, C. Saggese, T. Faravelli, E. Ranzi, A wide range kinetic modeling study of pyrolysis and oxidation of methyl butanoate and methyl decanoate. Note II: Lumped kinetic model of decomposition and combustion of methyl esters up to methyl decanoate, Combustion and Flame, 159 (2012), pp. 22802294

hal-00846052, version 1 - 18 Jul 2013

[148] C. Saggese, A. Frassoldati, A. Cuoci, T. Faravelli, E. Ranzi, A lumped approach to the kinetic modeling of pyrolysis and combustion of biodiesel fuels, Proceedings of the Combustion Institute, 34 (2013), pp. 427434 [149] F. Buda, R. Bounaceur, V. Warth, P.A. Glaude, R. Fournet, F. Battin-Leclerc, Progress toward a unified detailed kinetic model for the autoignition of alkanes from C4 to C10 between 600 and 1200 K, Combustion and Flame, 142 (2005), pp. 170 186 [150] J. Biet, M.H. Hakka, V. Warth, P.A. Glaude, F. Battin-Leclerc, Experimental and modeling study of the low-temperature oxidation of large alkanes, Energy & Fuels, 22 (2008), pp. 22582269 [151] S. Touchard, R. Fournet, P.A. Glaude, V. Warth, F. Battin-Leclerc, G. Vanhove et al., Modeling of the oxidation of large alkenes at low temperature, Proceedings of the Combustion Institute, 30 (2005), pp. 10731081 [152] F. Battin-Leclerc, J. Biet, R. Bounaceur, G.M. Cme, R. Fournet, P.A. Glaude et al., EXGAs-ALKANES-ESTERS: a software for automatic generation of mechanisms for the oxidation of alkanes and esters, LRGP, Nancy, France (2010) [153] P.A. Glaude, O. Herbinet, S. Bax, J. Biet, V. Warth, F. Battin-Leclerc, Modeling of the oxidation of methyl esters validation for methyl hexanoate, methyl heptanoate, and methyl decanoate in a jet-stirred reactor, Combustion and Flame, 157 (2010), pp. 20352051 [154] E.R. Ritter, J.W. Bozzelli, THERM: thermodynamic property estimation for gas phase radicals and molecules, International Journal of Chemical Kinetics, 23 (1991), pp. 767778 [155] C. Muller, V. Michel, G. Scacchi, G.M. Cme, A computer program for the evaluation of thermochemical data of molecules and free radicals in the gas phase, Journal of Chemical Physics, 92 (1995), pp. 11541177 [156] S.W. Benson, Thermochemical kinetics, (2nd ed.)John Wiley and Sons, Inc., New York (1976) [157] V. Warth, N. Stef, P.A. Glaude, F. Battin-Leclerc, G. Scacchi, G.M. Cme, Computer-aided derivation of gas-phase oxidation mechanism: application to the modeling of the oxidation of n-butane, Combustion and Flame, 114 (1998), pp. 81 102 [158] R.J. Kee, F.M. Rupley, J.A. Miller, Chemkin II: a Fortran chemical kinetics package for the analysis of gas phase chemical kinetics, (1993) Sandia Laboratories Report SAND 89-8009B Livermore, CA: <http://www.reactiondesign.com/>. [159] P. Dagaut, N. Smoucovit, M. Cathonnet, Methyl acetate oxidation in a JSR: experimental and detailed kinetic modeling study, Combustion Science and Technology, 127 (1997), pp. 275291 [160] L. Gasnot, V. Decottignies, J.F. Pauwels, Kinetics modeling of ethyl acetate oxidation in flame conditions, Fuel, 84 (2005), pp. 505518

71

[161] P. Osswald, U. Struckmeier, T. Kasper, K. Kohse-Hinghaus, J. Wang, T.A. Cool et al., Isomer-specific fuel destruction pathways in rich flames of methyl acetate and ethyl formate and consequences for the combustion chemistry of esters, Journal of Physical Chemistry A, 111 (2007), pp. 40934101 [162] C.K. Westbrook, W.J. Pitz, P.R. Westmoreland, F.L. Dryer, M. Chaos, P. Osswald et al., A detailed chemical kinetic reaction mechanism for oxidation of four small alkyl esters in laminar premixed flames, Proceedings of the Combustion Institute, 32 (2009), pp. 221228 [163] L. Gasnot, V. Decottignies, J.F. Pauwels, Ethyl acetate oxidation in flame condition: an experimental study, Fuel, 83 (2004), pp. 463470 [164] A.J. Marchese, M. Angioletti, F.L. Dryer, Flow reactor studies of surrogate biodiesel fuels. In: Thirtieth international symposium on combustion, Work-in progress poster 1F1-03, http://www.princeton.edu.bases-doc.univ-lorraine.fr/ combust/posters/1F1-03%20Biodiesel.pdf (2004) [165] W.R. Schwartz, C.S. McEnally, L.D. Pfefferle, Decomposition and hydrocarbon growth process for esters in nonpremixed flames, Journal of Physical Chemistry A, 110 (2006), pp. 66436648 [166] S. Gal, M. Thomson, S.M. Sarathy, S.A. Syed, P. Dagaut, P. Divart et al., A wide-ranging kinetic modeling study of methyl butanoate combustion, Proceedings of the Combustion Institute, 31 (2007), pp. 305311

hal-00846052, version 1 - 18 Jul 2013

[167] W.K. Metcalfe, S. Dooley, H.J. Curran, J.M. Simmie, A.M. El-Nahas, M.V. Navarro, Experimental and modeling study of C5H10O2 ethyl and methyl esters, Journal of Physical Chemistry A, 111 (2007), pp. 40014014 [168] S.M. Sarathy, S. Gal, S.A. Syed, M.J. Thomson, P. Dagaut, A comparison of saturated and unsaturated C4 fatty acid methyl esters in an opposed flow diffusion flame and jet stirred reactor, Proceedings of the Combustion Institute, 31 (2007), pp. 10151022 [169] S. Gal, S.M. Sarathy, M.J. Thomson, P. Divart, P. Dagaut, Experimental and chemical kinetic modeling study of small methyl esters oxidation: methyl (E)-2-butenoate and methyl butanoate, Combustion and Flame, 155 (2008), pp. 635650 [170] S. Dooley, H.J. Curran, J.M. Simmie, Autoignition measurements and a validated kinetic model for the biodiesel surrogate, methyl butanoate, Combustion and Flame, 153 (2008), pp. 232 [171] S.M. Walton, M.S. Wooldridge, C.K. Westbrook, An experimental investigation of structural effects on the autoignition properties of two C5 esters, Proceedings of the Combustion Institute, 32 (2009), pp. 255262 [172] K. HadjAli, M. Crochet, G. Vanhove, M. Ribaucour, R. Minetti, A study of the low temperatures autoignition of methyl esters, Proceedings of the Combustion Institute, 32 (2009), pp. 239246 [173] A. Farooq, D.F. Davidson, R.K. Hanson, L.K. Huynh, A. Violi, An experimental and computational study of methyl ester decomposition pathways using shock tubes, Proceedings of the Combustion Institute, 32 (2009), pp. 247253 [174] M.H. Hakka, H. Bennadji, J. Biet, M. Yahyaoui, B. Sirjean, V. Warth et al., Oxidation of methyl and ethyl butanoates, International Journal of Chemical Kinetics, 42 (2010), pp. 226252 [175] B. Akih-Kumgeh, J.M. Bergthorson, Comparative study of methyl butanoate and n-heptane high temperature autoignition, Energy & Fuels, 24 (2010), pp. 24392448 [176] A. Farooq, W. Ren, K.Y. Lam, D.F. Davidson, R.K. Hanson, C.K. Westbrook, Shock tube studies of methyl butanoate pyrolysis with relevance to biodiesel, Combustion and Flame, 159 (2012), pp. 32353241 [177] Y.L. Wang, Q. Feng, F.N. Egolfopoulos, T.T. Tsotsis, Studies of C4 and C10 methyl ester flames, Combustion and Flame, 158 (2011), pp. 15071519 [178] S. Dooley, M. Uddi, S.H. Won, F.L. Dryer, Y. Ju, Methyl butanoate inhibition of n-heptane diffusion flames through an evaluation of transport and chemical kinetics, Combustion and Flame, 159 (2012), pp. 13711384 [179] W. Liu, A.P. Kelley, C.K. Law, Non-premixed ignition, laminar flame propagation and mechanism reduction of nbutanol, iso-butanol and methyl butanoate, Proceedings of the Combustion Institute, 33 (2011), pp. 9951002

72

[180] B. Yang, C.K. Westbrook, T.A. Cool, N. Hansen, K. Kohse-Hinghaus, Fuel-specific influences on the composition of reaction intermediates in premixed flames of three C5H10O2 ester isomers, Physical Chemistry and Chemical Physics, 13 (2011), pp. 69016913 [181] B. Yang, C.K. Westbrook, T.A. Cool, N. Hansen, K. Kohse-Hinghaus, Photoionization mass spectrometry and modeling study of premixed flames of three unsaturated C5H8O2 esters, Proceedings of the Combustion Institute, 34 (2013), pp. 443 451 [182] G. Dayma, S. Gal, P. Dagaut, Experimental and kinetic modeling study of the oxidation of methyl hexanoate, Energy & Fuels, 22 (2008), pp. 14691479 [183] G. Dayma, C. Togb, P. Dagaut, Detailed kinetic mechanism for the oxidation of vegetable oil methyl esters: new evidence from methyl heptanoate, Energy & Fuels, 23 (2009), pp. 42544268 [184] G. Dayma, S.M. Sarathy, C. Togb, C. Yeung, M.J. Thomson, P. Dagaut, Experimental and kinetic modeling of methyl octanoate oxidation in an opposed-flow diffusion flame and a jet-stirred reactor, Proceedings of the Combustion Institute, 33 (2011), pp. 10371043 [185] B. Rotavera, E.L. Petersen, Ignition behavior of pure and blended methyl octanoate, n-nonane, and methylcyclohexane, Proceedings of the Combustion Institute, 34 (2013), pp. 435442 [186] J.P. Szybist, J. Song, M. Alam, A.L. Boehman, Biodiesel combustion, emissions and emission control, Fuel Processing Technology, 88 (2007), pp. 679691 [187] J.P. Szybist, A. Boehman, D.C. Haworth, H. Koga, Premixed ignition behavior of alternative diesel fuel-relevant compounds in a motored engine experiment, Combustion and Flame, 149 (2007), pp. 112128 [188] K. Seshadri, T. Lu, O. Herbinet, S. Humer, U. Niemann, W. Pitz et al., Experimental and kinetic modeling study of extinction and ignition of methyl decanoate in laminar non-premixed flows, Proceedings of the Combustion Institute, 32 (2009), pp. 10671074 [189] S.M. Sarathy, M.J. Thomson, W.J. Pitz, T. Lu, An experimental and kinetic modeling study of methyl decanoate combustion, Proceedings of the Combustion Institute, 33 (2011), pp. 399405 [190] O. Herbinet, P.A. Glaude, V. Warth, F. Battin-Leclerc, Experimental and modeling study of the thermal decomposition of methyl decanoate, Combustion and Flame, 158 (2011), pp. 12881300 [191] S.P. Pyl, K.M. Van Geem, M.K. Sabbe, M.F. Reyniers, G.B. Marin, A comprehensive study of methyl decanoate pyrolysis, Energy, 43 (2012), pp. 146160 [192] W. Wang, M.A. Oehlschlaeger, A shock tube study of methyl decanoate autoignition at elevated pressures, Combustion and Flame, 159 (2012), pp. 476481 [193] D.R. Haylett, D.F. Davidson, R.K. Hanson, Ignition delay times of low-vapor-pressure fuels measured using an aerosol shock tube, Combustion and Flame, 159 (2012), pp. 552561 [194] M.H. Hakka, P.A. Glaude, O. Herbinet, F. Battin-Leclerc, Experimental study of the oxidation of large surrogates for diesel and biodiesel fuels, Combustion and Flame, 156 (2009), pp. 21292144 [195] S. Bax, M.H. Hakka, P.A. Glaude, O. Herbinet, F. Battin-Leclerc, Experimental study of the oxidation of methyl oleate in a jet-stirred reactor, Combustion and Flame, 157 (2010), pp. 12201229 [196] M.F. Campbell, D.F. Davidson, R.K. Hanson, C.K. Westbrook, Ignition delay times of methyl oleate and methyl linoleate behind reflected shock waves, Proceedings of the Combustion Institute, 34 (2013), pp. 419425 [197] P. Dagaut, S. Gal, M. Sahasrabudhe, Rapeseed oil methyl ester oxidation over extended ranges of pressure, temperature, and equivalence ratio: experimental and modeling kinetic study, Proceedings of the Combustion Institute, 31 (2007), pp. 29552961 [198] F. Billaud, V. Dominguez, P. Broutin, C. Busson, Production of hydrocarbons by pyrolysis of methyl-esters from rapeseed oil, Journal of the American Oil Chemists' Society, 72 (1995), pp. 11491154

hal-00846052, version 1 - 18 Jul 2013

73

[199] C.T. Chong, S. Hochgreb, Measurements of laminar flame speeds of liquid fuels: Jet-A1, diesel, palm methyl esters and blends using particle imaging velocimetry (PIV), Proceedings of the Combustion Institute, 33 (2011), pp. 979986 [200] P. Dagaut, S. Gal, Chemical kinetic study of the effect of a biofuel additive on jet-A1 combustion, Journal of Physical Chemistry A, 111 (2007), pp. 39924000 [201] H.P. Ramirez, K. Hadj-Ali, P. Divart, G. Dayma, C. Togb, G. Morac et al., Oxidation of commercial and surrogate bioDiesel fuel (B30) in a jet-stirred reactor at elevated pressure: experimental and modeling kinetic study, Proceedings of the Combustion Institute, 33 (2011), pp. 375382 [202] W.K. Metcalfe, C. Togb, P. Dagaut, H.J. Curran, J.M. Simmie, A jet-stirred reactor and kinetic modeling study of ethyl propanoate oxidation, Combustion and Flame, 156 (2009), pp. 250260 [203] H. Bennadji, P.A. Glaude, L. Coniglio, F. Billaud, Experimental and kinetic modeling study of ethyl butanoate oxidation in a laminar tubular plug flow reactor, Fuel, 90 (2011), pp. 32373253 [204] G. Dayma, F. Halter, F. Foucher, C. Togb, C. Mounaim-Rousselle, P. Dagaut, Experimental and detailed kinetic modeling study of ethyl pentanoate (ethyl valerate) oxidation in a jet stirred reactor and laminar burning velocities in a spherical combustion chamber, Energy & Fuels, 26 (2012), pp. 47354748 [205] Y. Zhang, A.L. Boehman, Experimental study of the autoignition of C8H16O2 ethyl and methyl esters in a motored engine, Combustion and Flame, 157 (2010), pp. 546555

hal-00846052, version 1 - 18 Jul 2013

[206] T.H. Lay, J.W. Bozzelli, A.M. Dean, E.R. Ritter, Hydrogen atom bond increments for calculation of thermodynamic properties of hydrocarbon radical species, Journal of Physical Chemistry, 99 (1995), pp. 1451414527 [207] H.J. Curran, P. Gaffuri, W.J. Pitz, C.K. Westbrook, A comprehensive modeling study of iso-octane oxidation, Combustion and Flame, 129 (2002), pp. 253280 [208] E.M. Fisher, W.J. Pitz, H.J. Curran, C.K. Westbrook, Detailed chemical kinetic mechanisms for combustion of oxygenated fuels, Proceedings of the Combustion Institute, 28 (2000), pp. 15791586 [209] R. Sumathi, W.H. Green Jr., Oxygenate, oxyalkyl, and alkoxycarbonyl thermochemistry and rates for hydrogen abstraction from oxygenates, Physical Chemistry and Chemical Physics, 5 (2003), pp. 34023417 [210] C.M. Lund, L. Chase, HCT-A general computer program for calculating time dependent phenomena involving onedimensional hydrodynamics, transport, and detailed chemical kinetics, (1995) Lawrence Livermore National Laboratory report UCRL-52504, revised. Livermore, CA. [211] G.P. Smith, D.M. Golden, M. Frenklach, M.N.W. Moriarty, B. Eiteneer, M. Goldenberg et al., GRI-Mech 3.0 web site, http://www.me.berkeley.edu/gri_mech/ (1999) [212] S.R. Hoffmann, J. Abraham, A comparative study of n-heptane, methyl decanoate, and dimethyl ether combustion characteristics under homogeneous-charge compression-ignition engine conditions, Fuel, 88 (2009), pp. 10991108 [213] O. Herbinet, J. Biet, M.H. Hakka, V. Warth, P.A. Glaude, A. Nicolle et al., Modeling study of the low-temperature oxidation of large methyl esters from C11 to C19, Proceedings of the Combustion Institute, 33 (2011), pp. 391398 [214] P. Divart, S.H. Won, S. Dooley, F.L. Dryer, Y. Ju, A kinetic model for methyl decanoate combustion, Combustion and Flame, 159 (2012), pp. 17931805 [215] A. Ristori, P. Dagaut, M. Cathonet, The oxidation of n-hexadecane: experimental and detailed kinetic modelling, Combustion and Flame, 125 (2001), pp. 11281137 [216] V.I. Golovitchev, J. Yang, Construction of combustion models for rapeseed methyl ester bio-diesel fuel for internal combustion engine applications, Biotechnology Advances, 27 (2009), pp. 641655 [217] H.J. Curran, P. Gaffuri, W.J. Pitz, C.K. Westbrook, A comprehensive modeling study of n-heptane oxidation, Combustion and Flame, 114 (1998), pp. 149177 [218] B.I. Parsons, C.J. Dandy, The oxidation of hydrocarbons and their derivatives. Part I: The observation of the progress of the reaction by pressure change and by analysis, Journal of the Chemical Society (1956), pp. 17951798

74

[219] B.I. Parsons, C. Hinshelwood, The oxidation of hydrocarbons and their derivatives. Part II: Structural effects in the ester series, Journal of the Chemical Society (1956), pp. 17991803 [220] B.I. Parsons, The oxidation of hydrocarbons and their derivatives. Part III. The role of intermediates, Journal of the Chemical Society (1956), pp. 18041809 [221] D.E. Hoare, T.M. Li, A.D. Walsh, Cool flames and molecular structure, Proceedings of the Combustion Institute, 11 (1967), pp. 879887 [222] A.E. Lutz, R.J. Kee, J.A. Miller, SENKIN: A Fortran program for predicting homogeneous gas phase chemical kinetics with sensitivity analysis, (1988) Sandia National Laboratories Sandia report SAND87-824B. San Diego, CA http://www.sandia.gov/chemkin/docs/senkin.pdf [223] P. Dagaut, G. Pengloan, A. Ristori, Oxidation, ignition and combustion of toluene: experimental and detailed chemical kinetic modelling, Physical Chemistry and Chemical Physics, 4 (2002), pp. 18461854 [224] M. O'Conaire, H.J. Curran, J.M. Simmie, W.J. Pitz, C.K. Westbrook, A comprehensive modeling study of hydrogen oxidation, International Journal of Chemical Kinetics, 36 (2004), pp. 603622 [225] A.M. El-Nahas, M.V. Navarro, J.M. Simmie, J.W. Bozzelli, H.J. Curran, S. Dooley et al., Enthalpies of formation, bond dissociation energies and reaction paths for the decomposition of model biofuels: ethyl propanoate and methyl butanoate, Journal of Physical Chemistry A, 11 (2007), pp. 37273739

hal-00846052, version 1 - 18 Jul 2013

[226] H.J. Curran, Rate constant estimation for C1 to C4 alkyl and alkoxyl radical decomposition, International Journal of Chemical Kinetics, 38 (2006), pp. 250275 [227] Y.R. Luo, Handbook of bond dissociation energies in organic compounds, CRC Press, Boca Raton, FL (2003) [228] Goodwin DG., An open-source extensible software suite for CVD process simulation. In: Proceedings of CVD XVI and EuroCVD fourteen, Electrochemical Society, vol. 14; 2003. p. 15562. [229] L.K. Huynh, A. Violi, Thermal decomposition of methyl butanoate: ab initio study of a biodiesel fuel surrogate, The Journal of Organic Chemistry, 73 (2008), pp. 94101 [230] A.J. Marchese, T.L. Vaughn, K. Kroenlein, F.L. Dryer, Ignition delay of fatty acid methyl ester fuel droplets: microgravity experiments and detailed numerical modelling, Proceedings of the Combustion Institute, 33 (2011), pp. 20212030 [231] R.A. Yetter, F.L. Dryer, Inhibition of moist carbon monoxide oxidation by trace amounts of hydrocarbons, Proceedings of the Combustion Institute, 24 (1992), pp. 757767 [232] D.F. Davidson, J.T. Herbon, D.C. Horning, R.K. Hanson, OH concentration time histories in n-alkane oxidation, International Journal of Chemical Kinetics, 33 (2001), pp. 775783 [233] P.A. Glaude, W.J. Pitz, M.J. Thomson, Chemical kinetic modeling of dimethyl carbonate in an opposed-flow diffusion flame, Proceedings of the Combustion Institute, 30 (2005), pp. 11111118 [234] C.J. Hayes, D.R. Burgess Jr., Exploring the oxidative decomposition of methyl esters: methyl butanoate and methyl pentanoate as model compounds for biodiesel, Proceedings of the Combustion Institute, 32 (2009), pp. 263270 [235] R.J. Kee, F.M. Rupley, J.A. Miller, M.E. Coltrin, J.F. Gear, E. Meeks, Theory manual CHEMKIN Release 4.0.1, Reaction Design, Inc. (2004) [236] S.S. Ahmed, Kinetic modeling study on the effect of methyl decanoate addition to diesel surrogates in an HCCI engine, Proceedings of the fifth European combustion meeting, Cardiff University (28 June1 July 2011) http://data.cas.manchester.ac.uk/database3/SAMPLE%20III/Dropbox%20stuff/ECM/ECM%202011%20Papers/182.pdf [237] Naik CV, Pitz WJ, Sjoberg M, Dec JE, Orme J, Curran HJ, et al. Detailed chemical kinetic modeling of surrogate fuels for gasoline and application to an HCCI engine. In: SAE fall powertrain and fluid systems conference & exhibition, San Antonio, Texas, SAE paper 2005-01-3742; 2005. [238] C.K. Westbrook, W.J. Pitz, O. Herbinet, H.J. Curran, E. Silke, A detailed chemical kinetic reaction mechanism for nalkane hydrocarbons from n-octane to n-hexadecane, Combustion and Flame, 156 (2009), pp. 181199

75

[239] J.R. Pedersen, A. Ingemarsson, J.O. Olsson, Oxidation of rapeseed oil, rapeseed methyl ester (RME) and diesel fuel studied with GC/MS, Chemosphere, 38 (1999), pp. 24672474 [240] V.I. Golovitchev, accessed (2003) http://www.tfd.chalmers.se/valeri/MECH.html [241] A.A. Amsden, KIVA-3V, a block-structured KIVA program for engines with vertical or canted valves, (1997) Report LA13313-MS, UC-1412. Los Alamos, New Mexico [242] D.A. Kairaitis, V.R. Stimson, The thermal decompositions of ethyl trans-crotonate and ethyl n-butyrate, Australian Journal of Chemistry, 21 (1968), pp. 13491354 [243] C.K. Westbrook, Chemical kinetics of hydrocarbon ignition in practical combustion systems, Proceedings of the Combustion Institute, 28 (2000), pp. 15631577 [244] L.K. Huynh, K.C. Lin, A. Violi, Kinetic modeling of methyl butanoate in shock tube, Journal of Physical Chemistry A, 112 (2008), pp. 1347013480 [245] A. Osmont, M. Yahyaoui, L. Catoire, I. Gkalp, M.T. Swihart, Thermochemistry of CO, (CO)O, and (CO)C bond breaking in fatty acid methyl esters, Combustion and Flame, 155 (2008), pp. 334342 [246] C.K. Westbrook, W.J. Pitz, H.J. Curran, Chemical kinetic modeling study of the effects of oxygenated hydrocarbons on soot emissions from diesel engines, Journal of Physical Chemistry A, 110 (2006), pp. 69126922

hal-00846052, version 1 - 18 Jul 2013

[247] T.X. Li, D.L. Zhu, N.K. Akafuah, K. Saito, C.K. Law, Synthesis, droplet combustion, and sooting characteristics of biodiesel produced from waste vegetable oils, Proceedings of the Combustion Institute, 33 (2011), pp. 20392046 [248] A. Osmont, L. Catoire, I. Gkalp, Thermochemistry of methyl and ethyl esters from vegetable oils, International Journal of Chemical Kinetics, 39 (2007), pp. 481491 [249] A. Osmont, L. Catoire, I. Gkalp, M.T. Swihart, Thermochemistry of CC and CH bond breaking in fatty acid methyl esters, Energy & Fuels, 21 (2007), pp. 20272032 [250] A. Osmont, L. Catoire, P. Dagaut, Thermodynamic data for the modeling of the thermal decomposition of biodiesel. 1. Saturated and monounsaturated FAMEs, Journal of Physical Chemistry, 114 (2010), pp. 37883795

76