Beruflich Dokumente
Kultur Dokumente
Jermaine A. Lamboso
Jhonnielyn Joy T. Fidel
Jireh Jan S. Villamor
Blesy May G. Tolentino
Wayne Laurence Bobon
CHAPTER 1
Introduction
As the leading industry in Negros, sugar production creates waste by-products that can
still be tapped for added profitability. A prime example of this is bagasse, the fibrous residue in
the extraction of cane juice, which is now used as biomass for boiler operations and sometimes
for the plants power grid (Bangcoguis, 2007). The burning of bagasse leaves an ash residue,
another by-product that can be recycled as land fill and filler for building materials (Affandi,
Setyawan, Winardi, Purwanto, & Balgis, 2009). This study aims to create added value for
sugarcane bagasse ash when processed to produce silicon (Si), a valuable material whose
applications range from aluminum and ferrous alloys for construction, to solar panels for
renewable energy, to semiconductors for electronics.
High purity silicon (98-99.99% Si) has been studied as an alternative to metallurgicalgrade silicon (MG-Si) for industrial uses. Metallurgical-grade silicon (MG-Si) with purity
usually at 98% Si is processed from quartz sand (primarily SiO2). It serves as the raw material
for the production of solar-grade (99.9999% Si) and electronic-grade silicon (99.9999999% Si)
in photovoltaic and electronic industries respectively. Previous studies have produced high
purity silicon from plant biomass such as rice husks as a cheap alternative source of silicon
dioxide (SiO2), instead of quartz sand (Lund, Zhang, Jennings, & Singh, 2000). Quartz sand is
obtained by sand mining, which has detrimental effects to the environment like land degradation,
erosion, fissures, and adverse effects to water supply and quality (Saviour, 2012). The use of
plant biomass as the source of silicon instead of quartz sand may address this environmental
concern. Like rice husks, sugarcane bagasse ash is also rich in SiO2 (Abrasia, Alabado, Etang, &
Taton, 2002), making it a viable source for the production of high purity silicon. The extraction
of high purity silicon from sugarcane bagasse ash not only adds economic value to this waste
material and increases process efficiency for the sugar industry, but also promotes environmental
care by being an alternative to mining activities.
1.1 Objectives of the Study
The primary objective of this study is to extract high purity silicon from sugarcane bagasse
ash. Specifically, it aims to:
1.) Determine the parameters that affect the extraction of high purity silicon
2.) Devise and perform a method in extracting high purity silicon (Si) from sugarcane
bagasse ash
3.) Determine the purity of silica (SiO2) obtained from sugarcane bagasse ash
4.) Characterize the final product (Si) according to its purity and impurity concentrations
1.2 Significance of the Study
The study may be significant to the following:
Chemists and chemical engineers. Through this study, chemists and chemical engineers
may be inspired to further develop novel procedures in converting a waste material to a
significant raw material. They may also have the chance to improve existing procedures so as to
increase efficiency and further optimization.
Laboratories and Integrated Scientific and Industrial Supply. Quantitative analyses of the
samples and end-product are to be done by an external institution, National Institute of
Geological Sciences UP Diliman (NIGS).
CHAPTER 2
Review of Related Literature
2.1 Silicon and its properties, types, and uses
Silicon, with the chemical symbol Si, is the second member in Group 14, formerly known
as Group IV-A, of the periodic table of elements. It is characterized as a metalloid whose atomic
number is 14 with an electronic configuration of [Ne] 3s2 3p2. Dating back 1824, Jns Jakob
Berzelius discovered silicon whose name was derived from silex or silicis meaning flint. It
occurs in the solid state at room temperature and its melting and boiling points are 1414C and
3265C respectively (Royal Chemical Society, 2015).
Second only to oxygen in terms of abundance on the earths crust (approximately 28% by
mass Si), silicon is naturally found as 92%
28
atomic mass at 28.085 (Nave, 2015). It has a gray and lustrous appearance, and crystallizes in a
diamond-cubic structure. Crystalline forms of silicon include monocrystalline, polycrystalline,
and amorphous silicon. The monocrystalline type or single-crystal silicon is the purest form of
silicon, characterized by its homogeneous crystal framework and lack of grain boundaries. It is
commonly used in producing solar cells and is more efficient than the cheaper polycrystalline
type (Heywang et al, 2004). Polycrystalline silicon, on the other hand, is not as homogeneous as
single-crystal silicon as its framework is made up of multiple smaller crystals. It is more costeffective to produce commercially, thus its wide use in electronics and photovoltaics as well
(Fraunhofer Institute, 2014). Amorphous silicon is a noncrystalline allotrope of silicon used in
photovoltaics that require low power and in production of thin film transistors. A pocket
calculators solar cell is usually amorphous silicon (New Scientist, 1985).
Silicon used in the industry is classified according to their purity. There are three
categories by which silicon is sorted out metallurgical grade, solar grade and electronic grade.
Safarian et al. (2012) stated that metallurgical grade silicon (MG-Si) is the initial material used
for producing the other classifications. MG-Si produced through the industrial process is 98-99%
pure with remnants of other elements like iron, aluminum, titanium, vanadium, boron, and
phosphorus which affects the efficiency of solar grade silicon (SG-Si) and electronic grade
silicon (EG-Si). SG-Si is the type applicable for the photovoltaic industry for use in
manufacturing solar panel wafers. However, before they can be utilized in the solar industry they
must be purified up to 99.9999% (6N). In order to qualify for EG-Si, 99.999999% (8N) or higher
purity of silicon must be achieved (Fishman, 2008).
Most of the worlds silicon production is used to make alloys including aluminum-silicon
and ferro-silicon (iron-silicon). Silicones, or silicon-oxygen polymers, is also considered as an
extensive use for silicon. Silicone oil is a lubricant added to hair products and cosmetics.
Silicone rubber is also used as sealant in bathrooms, windows, pipes, and roofs. Sand (silicon
dioxide or silica) and clay (aluminum silicate) are used to make concrete and cement, glass, and
various ceramics. Silicon carbides have applications in abrasive and laser industries. Most
common of all is the use of silicon as a semiconductor in computer, microelectronics, and
photovoltaic industries (Royal Chemical Society, 2015).
2.2 Silicon economy in the Philippines
According to The World Factbook by the United States Central Intelligence Agency
(2015), the Philippines primarily exports semiconductors and electronic products, transport
equipment, garments, copper products, petroleum products, coconut oil, fruits.
A recent report by the Department of Trade and Industry showed that semiconductors and
electronic products are the countrys top export, accounting for 45.96% of export goods as of
April 2015. In 2014, Philippines earned $16,913,341,592.66 on integrated circuits alone (Simoes,
2014).
The non-stock, non-profit organization Semiconductor and Electronics Industries in the
Philippines, Inc. or SEIPI has presented that in order to maintain the growth of the electronics
industry in the country, manufacturing cost control and silicon wafer fabrication for
semiconductors are areas that need to be developed in the country. Presently, the country imports
all materials abroad and only focuses on test and assembly of semiconductors and electronics.
Manufacturing the raw materials here in the country could be an advantage for the electronics
sector, especially in reducing production costs and decreasing the reliance on imports from other
countries (Santiago, 2015).
2.3 Manufacture of silicon in the industry
Quartz sand, basically crystalline SiO2, is the raw material for the industrial production of
metallurgical-grade silicon or MG-Si whose purity ranges between 98-99%. The sand is reduced
by carbon at 1900C in an electric arc furnace. The majority of the worlds production is used as
raw material for the manufacture of steel and aluminum alloys, solar cell industries, and
electronics. The level of impurity in metallurgical-grade silicon is too high for photovoltaic and
microelectronics applications, thus the need for further purification steps in producing solarready and circuit-ready silicon (Koch and Rinke, 2014).
In the commercial-scale, electronic-grade silicon (EG-Si) is manufactured by the
commonly used process known as the Siemens process. It is at present the standard method for
purifying metallurgical-grade silicon (MG-Si) to 99.9999% pure polycrystalline silicon or use in
producing semiconductor devices and solar cells (Lund, Zhang, Jennings and Singh, 2000). This
is done according to the chemical reactions:
Metallurgical Si(s) + 3HCl(g) SiHCl3(g) + H2(g)
(reaction 1)
(reaction 2)
In this process according to Lund et al. (2000), trichlorosilane (SiHCl3) is first obtained
from bed of fine MG-Si particles. The metallurgical particle is fluidized and chlorinated with
hydrochloric acid with copper as the catalyst in the reaction. To reduce impurities, the impure
SiHCl3 then undergo succeeding fractional distillation. A chemical vapor deposition method is
subsequently used to produce the EG-Si from the high purity SiHCl3. Vaporized SiHCl3 is
decomposed and reduced with hydrogen at about 1000C, resulting to silicon deposit on an
inverted U-tube. The bridge is made of slim silicon rods and has been heated in a reactor by
passing an electric current through it. This process can produce six polycrystalline rods of 1 m
length and 12 cm diameter simultaneously. The obtained EG-Si has a purity of 99.9999999%
(9N purity).
Other growth techniques for photovoltaic applications are also available such as the wellknown Czochralski method and float-zone melting. The Czochralski method involves melting
10
sample was processed in a fluidized bed combuster with flowing argon and carbon dioxide at
950C. Carbothermic reduction of the ash subsequently ensued at 1900C, reportedly yielding
high purity silicon with impurities less than 75 ppm.
Hunt et al. (1984) investigated the feasibility of producing silicon with even higher purity
by improving the purification technique of Amick et al. through pelletizing of the reactants
before reduction with carbon black in a modified electric furnace. Their study claimed that their
purified rice husk ash is a viable candidate as raw material for solar grade silicon synthesis.
Ikram and Akther (1988) used high purity magnesium as a reductant, after preparation of
the rice husk ash by acid leaching in 1:10 hydrochloric acid and pyrolysis in a muffle furnace.
Additional acid purification with hydrochloric, hydrofluoric, and sulfuric acid was done after
reduction. The study reported a yield of 99.95% silicon with a Boron impurity of about 2ppm.
Surpassing Ikram and Akther with 99.9999% silicon purity, Singh and Dindaw (1978)
also used magnesium to reduce white rice husk ash at 800C with subsequent acid leaching
treatments. The authors also suggested the possibility of smelting the obtained silica with
carbonaceous reductants in a furnace, followed by acid purification, and to repeat the process
nine times. The analysis method to determine the purity of silicon however was not specified in
the paper.
Larbi (2010) also devised a method to synthesize 99.5% pure silicon from rice husks by a
pre-reduction acid treatment, reduction with magnesium, and a two-stage acid leaching process
using different mixtures of hydrofluoric, acetic, and hydrochloric acid. Boron impurity was less
than 3ppm. Highest silicon yield was achieved with a reduction temperature of 900C in argon
11
atmosphere and a charge with 5% excess magnesium. The obtained silicon was considered high
purity: greater than metallurgical-grade purity but less than electronic-grade.
Aminullah et al. (2015) extracted silicon dioxide from bamboo leaf ash by combusting
the leaves in open air and ashing the obtained residue in the furnace at 400C and then at 950C.
After acid leaching and filtration, the ash was again put in the furnace at 1000C to obtain silicon
dioxide. Magnesium was used as reducing agent, pyrolyzed at 650C for an hour. After acid
treatment with 3% HCl and drying, the resulting silicon obtained had a purity of only less than
10%. This was attributed to the type of acid used in leaching, which was insufficient to dissolve
impurities. The samples were characterized by Energy Dispersive X-ray (EDX) and Scanning
Electron Microscopy (SEM).
Mubarok et al. (2014) employed local hot mud as raw material for preparation of silicon.
Lapindo mud is an active spurt of hot mud from a drilling location in Indonesia classified as a
natural disaster. It had been found to be rich in silica content, inferentially a potential source for
silicon extraction. With the addition of sodium hydroxide, silica was extracted from the mud as
sodium silicate. Titration with hydrochloric acid, washing and drying then produced silica
xerogel. Reduction of the silica with magnesium at 650C for 3 hours and subsequent acid
leaching using hydrochloric, hydrofluoric, and acetic acid yielded silicon with 98.1% purity.
Characterization was done by X-ray diffraction and X-ray fluorescence.
Affandi et. al (2009) extracted silica (SiO2) xerogels with a purity of 99% from sugarcane
bagasse ash by employing the sodium silicate route by extraction by adding NaOH, titration with
HCl, gelation, and then drying. The study employed three methods to determine which produces
12
the best purity of SiO2, namely pretreatment acid washing with 1 M HCl, cation exchange resin
treatment, and post-treatment washing using demineralized water. Of the three methods, the
group concluded that using demineralized water was effective in improving purity to as high as
99%. The characterization of the produced silica (SiO2) xerogels was done by X-ray fluorescence
spectroscopy.
All of the abovementioned methods employ the same three basic steps in the production
of silicon(Si): pre-reduction treatment, reduction, and post-reduction treatment. This paper aims
to devise a method that also includes these three basic steps to obtain silica (SiO2) from
sugarcane bagasse ash with the appropriate and optimal parameters.
2.5 Sugarcane bagasse ash, its properties, and uses
Sugarcane bagasse ash (SCBA) is obtained as a solid waste from sugar industries. After
crushing of sugarcane in sugar mills and extraction of juice from processed cane by milling, the
discarded fibrous matter called bagasse is used as fuel to generate power and electricity in the
factory. Bagasse is burnt at to use its maximum fuel value and the residue after burning, namely
bagasse ash, is collected and disposed of as landfill. In order to maximize its potential, several
studies were conducted that aims to find other ways to utilize SCBA and increase its value in the
industry.
SCBA has benefited a number of different fields due to its remarkable properties. Studies
using SCBA as cement replacement in concrete (Kawade et al, 2013), alternative pozzolanic
material (Suliman et al., 2011) and supplementary cementitious material in concrete (Dhengare
et al, 2015) proves its effectiveness as a construction material. SCBA is also efficient when used
13
as adsorbent as shown by Kanawade et al. (2010) using bagasse ash in removing dyes from dye
effluent and brilliant green dyes from aqueous solutions (Mane et al, 2007). Teixeira et al.
(2010) also produced glass-ceramic materials from SCBA.
SCBA as a waste material from the burning of bagasse for power generation in sugarcane
industries can thus be recycled for its high silica content. A study conducted by Abrasia,
Alabado, Etang and Taton (2002), characterized SCBA acquired from First Farmers Holding
Corporation in Negros Occidental. Table 2.1 shows the different compounds that constitute
SCBA.
Table 2.1 Chemical composition of sugarcane bagasse ash*
Component
Composition (wt. %)
SiO2
76.10
Al2O3
14.76
CaO
3.48
Na2O
0.65
other components
5.01
14
The conversion of insoluble silicates into sodium silicate through high temperature fusion
with other sodic bases is the traditional method of determining the silicon content of different
materials (Silicon in Agriculture, 2001). With the continuing advance research of silicon around
the world, different methods of silicon content determination have been developed including
gravimetric, colorimetric and absorption/emission spectroscopy (Dai et. al, 2005).
Gravimetric method is one of the classical quantitative analysis of silicon. In the analysis
of silicon in soils, the method begins with oxidation to remove organic matter, acid dissolution of
remaining components, filtration of silica precipitate, and finally ignition to recover silicon.
Gravimetric method uses simple laboratory equipment yet time consuming and strenuous to
work (Silicon in Agriculture, 2001).
Colorimetric analysis is a cheaper technique of quantifying silicon content of various
materials since it only uses standard analytical equipment in the laboratory. It is based on the
formation of yellow silicomolybdic acid at higher silicon concentration that is further improved
to blue silicomolybdic acid procedure at lower silicon concentration using a reducing solution.
The latter is preferred because of its high sensitivity (Hogendorp, 2008).
X-Ray diffraction (XRD) is a rapid analytical technique used to determine the crystal
structure and crystalline phase of material. In the preparation of high purity silicon from raw rice
hulls (RRH) the high purity silicon in the form of white ash was found out to be polycrystalline
and amorphous respectively. The Raman Spectroscopy, technique that provides information also
about the physical characteristics such as crystalline phase and orientation of high purity silicon,
conformed to the results shown by XRD (Swatsitang et al., 2009).
15
Scanning Electron Microscopy (SEM) determines the surface structure, shape, particle
size, and morphology of the sample shown in the three-dimensional form (Worathanakul, 2009).
Larbi (2010) revealed the morphology of high purity silicon through SEM that was observed by
SEM micrograph showing the porosity of the prepared silicon due to acid leach. The combustion
of the organic component contributed to the porous morphology of rice hull ash (RHA).
Worathanakul et al. (2009) determined silica content in bagasse ash using x-ray
fluorescence spectroscopy (XRF). Bagasse ash was heated in the furnace at 600C, 700C, and
800C for three hours were analyzed through XRF and showed silica contents of 19.42%,
21.05% and 27.98% respectively. Subjecting the ash in acid treatment of 1M and 3M
hydrochloric acid and oxygen feeding in the furnace at 800C for 3 hours, silica content rose to
89.037%. From the analysis, Worathanakul et al. (2009) concluded that the increase in
temperature, acid treatment, and oxygen feeding removed most of the impurities in sugarcane
bagasse ash.
Larbi (2010) used inductively coupled plasma optical emission spectroscopy (ICP-OES)
or mass spectrometry (ICP-MS) to analyze the chemical composition of the final silicon powder
obtained from the second cycle leaching. Fifteen (15) mL of multiple-acid mixture was prepared
using the volume ratios of 1:1:1 deionized water, concentrated nitric acid (HNO3, 70 wt%),
concentrated hydrofluoric acid (HF, 48 wt%) in the respective order and used this to digest a
0.15 gram sample of the silicon powder in a closed Teflon beaker. The Teflon
(polytetrafluoroethylene) beaker and content was then heated to a temperature of 50-70 C for
half an hour. The totally digested sample was transferred to an HF-resistant 50-mL volumetric
flask or graduated cylinder. The sample solution was then filled up to the 50-mL mark with 2
16
vol% nitric acid solution for ICP-OES analysis. A blank solution was prepared with the same
ratios but with a volume factor of five less than the prepared sample solution. The calculation for
the impurity element (analyte) in the solid silicon sample is given by the following expression:
1000
mg
C ( L ) prep Vol (L)
(equation 2.1)
wt of Si (g)
Where, C is the difference between measured ICP-OES concentration of the analyte in the
sample and that in the blank solution.
When the difference results in a negative concentration, the minimum quantifiable
detection limit (D) of the ICP instrument for that analyte is used. The equation becomes
1000
mg
D ( L ) prep Vol (L)
wt of Si (g)
(equation 2.2)
Meanwhile, Swatsitang (2009) analyzed the obtained Si from rice hulls by XRD and
found to be polycrystalline Si as also confirmed by Raman spectra. Inductively Coupled Plasma
Atomic Emission Spectroscopy (ICP-AES) analysis confirmed metallic impurities such as Al,
Fe, Ca, Ni, Mn, Mg, Cu, Cr and Ti in the total range of 145 325 wt.ppm. About 99.98 % purity
of silicon was extracted from acid-treated RRH.
17
CHAPTER 3
Methodology
3.1 Research Design
This chapter aims to discuss in detail the experimental procedure of synthesizing high
purity silicon from sugarcane bagasse ash. Ash sample received from sugar factories in Negros
Occidental is subjected to an extraction treatment to yield silica (SiO2) xerogels. Metallothermic
reduction of SiO2 using magnesium (Mg) as reductant is carried out at a temperature of 650C in
a furnace. Subsequent acid leaching steps then ensue as post-reduction treatment to remove
unwanted soluble phases that may have formed after reduction. The product obtained is silicon
and is analyzed using energy dispersive X-ray fluorescence spectroscopy (EDXRF) A schematic
flowchart for the procedure is outlined in Figure 3.1.
XRF
Analysis
18
The list of required materials and reagents for the experiment, their description, and their
following sources are showed in Table 3.1.
Table 3.1 Materials and reagents needed for the experimental work
Material/Reagent
Description
Sodium Hydroxide
2 M aqueous solution
Magnesium Turnings
99 wt% pure
Source
First Farmers Holdings
Corporation
USLS College Science
Laboratory
USLS College Science
Laboratory
1 M aqueous solution
Hydrochloric Acid
3.3 Procedure
The synthesis of silicon from sugarcane bagasse ash is accomplished in three major steps:
purification treatment, reduction, and post-reduction treatment. Characterization of the raw
materials and quantitative analyses of the products are done through energy dispersive X-ray
fluorescence spectroscopy (EDXRF).
19
Bagasse Ash
Extraction with 2M NaOH
Filtration
Gelation
Aging
Slurry Formation
Washing
Drying
Fig. 3.2 Flow diagram of the procedure used to produce silica xerogels from SCBA
20
48g mol
60 g mol
(equation 3.2)
Adapted from Swatsitang & Krochai (2009), the post-reduction treatment of the
reduced product undergoes three leaching sequences. The first and second leaching
sequences are basically the same process: a mixture of hydrochloric acid and water with
volume ratio 1:2 is used as leaching reagent at room temperature for 10 minutes and then
repeated with a different reagent which is hydrofluoric acid in water 1:2 volume ratio.
21
Volume ratio
Temperature
Duration
Room temperature
10 minutes
Room temperature
10 minutes
95C
22
15 minutes
Characterization of the final product (Si) employs energy dispersive X-ray fluorescence
spectroscopy (EDXRF) for elemental analysis of the impurities in the product. This is to be done
by National Institute of Geological Sciences-UP Diliman (NIGS).
23
CHAPTER 4
Results and Discussion
This chapter presents the tabulation and analysis of data for the experimental study
according to the methodology as discussed in Chapter 3. It is divided into three sections
corresponding to the three main steps in the study namely preparation of SiO2, reduction of SiO2
to Si, and post-leaching treatment for the product. Findings from each of the step are presented
accordingly. Appendix A presents photos for the whole process. Appendix B provides a copy of
the official results from National Institute of Geological Sciences (NIGS), UP Diliman.
4.1 Preparation of Silica (SiO2) Xerogels
A mixture of 100g bagasse ash and 1 liter 2N NaOH was found to boil at a temperature of
96.5C for sample A and 97C for B. Two hundred and ninety (290) mL of yellow to brown
filtrate (sodium silicate) was obtained after filtration for A and 310 mL for B. The loss in volume
can be attributed to the evaporation of water from the mixture while boiling. This volume of
filtrate required 800 mL of 1 M HCl to reach a pH of 7 of A and 1015 mL for B. Silica xerogels
acquired after aging of 18h, washing, and drying in the oven for 12h had the appearance of large
white solid chunks with a total mass of 12g for A and 68.9g for B. The chunks were then ground
to powder form. Table 4.1 presents data acquired from the experimental study. Due to financial
constraints, only sample B was sent for analysis. Table 4.2 presents the composition of the
product sample B. Figure 4.1 shows the X-ray diffraction profile for the silica obtained for
sample B. Analysis was done using EDXRF or energy dispersive X-ray fluorescence at the
National Institute of Geological Sciences (NIGS), UP Diliman.
96.5C
97C
290 mL
310 mL
800 mL
1015 mL
12 g
68.9 g
%relative
concentration
54.87
Cl
40.39
K2O
3.16
SO3
1.17
Fe2O3
0.30
ZnO
0.05
CuO
0.03
Rb2O
0.02
24
25
Mass, g
With Mg
11.40
11.40
Without Mg
6.00
6.00
A
B
After reduction
9.56
9.12
Sample
Mass
Before post-leaching After post-leaching
8.00 g
2.19 g
8.00 g
3.15 g
Total Volume of
Acid
12 mL
12 mL
Sample
1:2 HF : H2O
HF
H2O
4 mL
8 mL
4 mL
4 mL
8 mL
26
8 mL
Total Volume of
Acid
22 mL
22 mL
Analyses by EDXRF of the constituents in final products A and B are presented in Table
4.8. X-ray diffraction profiles for the samples are presented in Figure 4.2 and 4.3.
Table 4.8 Relative concentrations of the constituents in final products A and B
Analyte, %
Product A
Product B
Si
94.33
83.32
Cu
0.06
0.96
Al
3.65
Fe
0.22
Pb
0.05
Po
0.05
Ir
0.04
1.33
Rb
0.02
Os
0.02
9.76
Mn
0.64
Sc
0.18
Zn
0.06
Ti
1.48
1.17
27
28
29
expected percent silica content of 99.16%. This silica was then reacted with Mg-ribbon through a
muffle furnace at 600oC for 12 hours. The reduced product underwent post leaching with HCl
and HF to leach out impurities. The obtained percent purity of the final product only reached
94.33% Si as the highest among the 2 samples as analyzed by XRF. Obtained silicon appears to
be brown in powdered form. It has been shown that Sugarcane Bagasse Ash (SCBA) is a good
raw material for the extraction of high purity Silicon (99% Si).
5.2 Conclusions
By conducting this experimentation and analyzing the product obtained in the extraction
of silicon from sugarcane bagasse ash, the following conclusions were derived:
1. The study successfully produced silicon from sugarcane bagasse ash from two
experimental runs.
2. The percentage of silica content is 54.87% as analyzed by XRF which is much lower than
the expected percent silica content of 99.16% based on the study of Affandi et al.
3. The obtained purity of the final product reached 94.33% Si as the highest between the 2
samples as analyzed by XRF. Obtained silicon appears to be dark brown in powdered
form.
5.3 Recommendations
The researchers would like to recommend the following for the improvement of the study
and future works:
30
1. Optimization of the different parameters such as temperature, contact time, and amounts
and concentrations of reagents for a certain amount of raw material may be investigated
to maximize the efficiency of the process.
2. Implementation of different methods and techniques of extracting silica with lesser time
and energy requirement may also be explored.
3. A larger scale study for the process may be carried out to determine the feasibility of the
process on a commercial-scale basis.
31
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