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Editor-in-Chief
Prof. Vishnu J. Gaikwad
Department of Biotechnology, TKIET, Warananagar, M.S., India.
Section Editor
Dr. Mahdi Esmaeilzadeh, Founder & Chairman of Scientific Research Publishing House
(SRPH), Mashhad, Iran
Co-Editor-in-Chief(s)
Prof. Kaushlendra Tripathi,
Mitchell cancer institute, USA.
Prof. E. S. NEHRU
Jubail University College, Jubail,Kingdom of Saudi Arabia
Prof. B.R.GURUPRASAD
Department of Biology, AET College, Kushal Nagar, Madikeri., INDIA
S. MILTON PRABU
Department of Zoology Annamalai university, India
Prof. P.Krishnamoorthy,
Department of Zoology, Rajah Serforji Government College, Thanjavur- 613 005, Tamil
Nadu, INDIA
Prof. Supriya Singh,
Division of Microbiology, Division of Biochemistry and Biotechnology, Centre for AIDS &
Related Diseases, National Centre for Disease Control, 22 Sham Nath Marg, Delhi, India.
Department of Obstetrics & Gynaecology, Maulana Azad Medical College, Delhi, India.
Prof. R. M. Gudmalwar
Department of Biotechnology Engineering, KITs College of Engineering, Kolhapur, India.
Associate Editor(s)
Dr. R. SATHISHKUMAR
Department of Biotechnology, Bharathiar University, Coimbatore- 641 046, Tamil Nadu,
India
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Comparative Analysis of Agricultural Land Use by Economic Entities in The Natalia P. Sidorova 212-222
Context Of Multistructurality (in food security)
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approach in caries spine patients
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brain injury
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hospital, Bahawalpur
Frequency of associated injuries in cases of spinal cord injury Musadaque Hussain 287-291
A case control study on non-alcoholic fatty liver disease in healthy individuals and Shahbaz Ahmed 298-304
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mellitus
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Frequency of contributing factors (multiparity and previous caesarean section) of Nergis Taj 317-323
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organs (Spleen, Thymus gland and local bursa) within mature malired duck to
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Evaluation of the Activity of Spring Wheat Extracts (TRITICUM AESTIVUM L.) Radik I. Safin 330-335
The Analysis of Microbiome & Bacterial Endophytes in Seeds during Evaluation of Shamil Z. Validov 336-340
Spring Wheat Varieties (TRITICUM AESTIVUM L.)
Modern Biological Products and Growth Stimulators in the Technology of Rustam M. Nizamov 341-347
Cultivation of Sunflower for Oilseeds
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Economic Efficiency
Numerical simulation of the subsoil condensation process and its impact on the Alexander F. Zhirkov 372-386
heat and moisture regime of the frozen soils
Analysis of Environmental Impact Assessment of Oil and Gas Complex Facilities Larisa GILYOVA 387-390
Study of the environmental Pollution as Sanitary Protection Zone Parameters and Marina 391-394
Sanitary Gaps of the Land and Property Complex of the Roshchino International PODKOVYROVA
Airport in Tyumen
Environmental and Economic Zoning of Specially Protected Natural Areas in the Larisa GILYOVA 395-398
Framework of Natural Resources Rational Use
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Study of the Level of Change in the Natural-Territorial Complex of the City of Anatoliy OLEYNIK 403-406
Tyumen
Development of a Territorial Model of Agricultural Land Use on a Landscape- Dmitriy KUCHEROV 407-410
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The Investigation of Arable Acreages Classification Providing the Rational Irina KURASHKO 411-415
Organization of Land Use
Methodology for Developing a Geographic diversity Information Resource for the Marina 416-420
Purposes of a Comprehensive Assessment of Specially Protected Areas (Based on PODKOVYROVA
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Tomsky District Materials
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local female population of Pakistan
Analysis of ectopic pregnancy among local population of Pakistan Bakhtiar Ahmed B. 452-456
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disease
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thyroidectomy
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Experience Tayyaba
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(IV) pulse pamidronate therapy in non-steroidal anti-inflammatory drugs
(NSAIDS) refractory ankylosing spondylitis
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population
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suspected of having Acute appendicitis
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to department of rheumatology PIMS hospital Islamabad
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Children and Adolescents
Severity and Mortality Prediction in Chronic Liver Disease using Child PUGH and Musarrat Rauf 519-524
MELD scales
Prevalence of allergic fungal rhino-sinusitis among patients with nasal polyps Md Wahid Saleem 525-531
Analysis of removal of drains and discharge of breast cancer surgery patients in Mumtaz Ahmad Khan 532-536
Pakistan
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Letrozole alone in females presenting with Polycystic Ovarian Syndrome
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4cm)as predictor of success of laparoscopic sleeve gastrectomy
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with beta thalassemia major
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feeding with "Lesnov`s ferment" Popova
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midline laparotomy with respect to incision time and blood loss
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patients Baloch
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kidney injury in patients presenting through a tertiary care hospital Khan
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Status of Soil
Michail A. 596-603
Formation of Grain of Intensive and Extensive Rice Varieties
Skazhennik
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Starch
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Khyber Pakhtunkhwa
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Pakistan Piracha
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in Pakistan
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patients with nephrotic syndrome
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glaucoma patients
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embryos of egg crosses with different egg shell color during the incubation period.
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care hospital
Clinical and Socio demographic profile of burn patients Kashif Ali 693-697
Correlation of the Cellular Composition of the Epithelial Layer and Its own Plastics Svetlana A. 698-703
of Muscular Shell of Body of the Stomach of Rabbits Veremeeva
Physico-chemical Properties, Microbial Analyses and Acceptability of Fern Sofia C. Naelga 704-711
(Diplazium esculentum (Retz.) Sw.) Pesto
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Role of Evacuation via Diaphoresis in the management of Chronic Renal Failure: Nazmeen 719-722
An Appraisal
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territory care hospital
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of Jordan Zaiton
Respiratory syncytial virus infection in domestic ruminants in Sudan Intisar K.S. 741-744
A study on distribution of cervical lymph node metastases in oral squamous cell Gulraiz Zulfiqar 745-750
carcinoma (OSCC)
Efficacy of Topical Tranexamic Acid Application for Dry Socket Prevention M. Asim Naqash 751-757
A cross sectional study on subclinical hypothyroidism at tertiary care hospital Arfa Jabeen 766-770
Effect of Acetylation Method on Characterization of Cellulose Acetate based Sago Angela Myrra Puspita 785-791
"hampas" Dewi
International Journal of Advanced Biotechnology and Research (IJABR)
ISSN 0976-2612, Online ISSN 2278–599X,
Vol-10, Issue-1, 2019, pp785-791
http://www.bipublication.com
Research Article
ABSTRACT
Sago waste is a potential source of cellulose but it has not been utilized properly. To improve the properties of
cellulose based sago waste, it can be done by acetylation process. The objective of this research was to
createcellulose acetate from sago waste with variation of acetic anhidride concentration. Microcrystalline cellulose
could be prepared from sago waste resulted in yield around 43% with 59% cellulose content. Acetylation process
was done to microcrystalline cellulose from sago waste. FTIR profiling showed thatthe replacement of the acetyl
groups on hydroxyl groups was done with acetate anhydride addition. Acetate anhydride concentration was
affected yield, acetyl group and degree of substitution. The suitable acetic anhydride volume of acetylation
process was 66 ml produced cellulose acetate with yield 85.33%, degree substitution2.16, and acetyl content
36.87%.
INTRODUCTION
Cellulose is the most abundant polysaccharides widely used is acetylation to improve cellulose
on earth. It is an important structural component compatibility and dispersion on solvent [4].
of plants, many forms of algae, and oomycetes Sago is a native plant of South East Asia.
[1].Because of its biodegradability and chemical Around 50% of the world sago plants grow in
stability, cellulose has been used for more than Indonesia [5] and 90% of that number grows in
150 years for paper, pharmaceutical compounds, Papua and Maluku Province of Indonesia [6].
and textiles [2]. In recent years, scientists also The commercial utilization of sago plant only
have been trying to maximize its potential as focused on the extraction of its starch with yield
packaging materials. However, the application only around 18.8 – 38.8% [7], whereas the waste
of this cellulose-based packaging is still not can be processed to other products.The
widely used. Several problems regarding its utilization of sago waste or ‘hampas’ has been
poor mechanical and barrier properties still need reported to produce biethanol [8], as biomass
to be solved by chemical and physical treatment source to produce biohydrogen [23] and oil spill
[3]. One of the chemical treatment that has been removal [24]. Sago ‘hampas’ is a lignocellulosic
Effect of Acetylation Method on Characterization of Cellulose Acetate based Sago “hampas”
by-product produced from sago palm pith after calculate the yield, water content, and cellulose
starch extraction. Sago ‘hampas’ contains content.
cellulose which has potentially as material to Cellulose Acetate Synthesis
produce bioplastic and other products. Cellulose Cellulose acetate synthesis was conducted
fibers have relatively high strength, high following Bahmid et al.method [10] with some
stiffness, and low density but unsoluble in modification. 10 gram of cellulose based sago
organic or incorganic solvent, so it has ‘hampas’and 100 ml glacial acetic acid were
limitation to utilize cellulose as material of mixed and stirred at 38°C for one hour. The
product like bioplastic.To improve cellulose mixture was added by 2 ml of H2SO4 and was
solubility, it can be done by acetylation. stirred for 45 min at 38°C. The variation volume
Solubility of cellulose acetate was influenced by of acetic anhydride 0, 30, 60 and 66 ml were
degree of substitution. A study on the synthesis added to the mixture, and the mixture were
of cellulose acetate based on sago ‘hampas’ has continuousle stirred at 38oC for one hour. After
not been done. This research was studied about that, 25 ml of distilled water and 50 ml of glacial
effect of acetate anhidride concentration on acetic acid were added in several portions for 30
cellulose acetate based sago ‘hampas’ minutes under stirring. The mixture was washed
characteristics.. with distilled water until the liquid became clear
using centrifugation at 1500 rpm for 15 minutes
MATERIALS AND METHOD for each washing. The sediment than was dried
MATERIALS at 50°C for 48 hours and grounded and sieved
The sago ‘hampas’was obtained from local using 50 mesh sieve.
farmer in Sorong Selatan, West Papua.
Chemical reagents p.a. qualified NaOH, HCl, Characterization of Cellulose Acetate
NaOCl, acetic acid glacial, H2SO4, acetate Cellulose acetate was measured its yield, water
anhydride and aquadest to produce content, degree of acetylation, and the
microcrystalline cellulose and acetylation characteristic of the profile. Yieldwas calculated
process. by the weight recorded before and after the
treatment. Water content was measured using
METHODS AOAC method [11]. FTIR spectra profilanalysis
Preparation Microcrystalline Cellulose based using Shimadzu IR Prestige 21 on scanning
Sago ‘hampas’ range 400 to 4000 nm was done to obtain the
Microcrystalline cellulose based sago profile of the materials.
‘hampas’was conducted following the method Determination of acetyl content was followed
obtained from Ahmad et al. method [9]. 24 g of based on Candido and Gonçalves method [12].
dried sago ‘hampas’ were refluxed with 240 mL 0.1 g cellulose acetate was soaked with 5 ml of
of 1M NaOH at 80°C for 1h and 36 mins to 0.25 NaOH and 5 ml of ethanol for 24 h.
solubilize the lignin and hemicellulose. Following the soaking, 10 ml of 0.25 M HCl
Following alkali treatment, the alkaline treated was added into the mixture and was left for 30
sago waste was washed and filtered until the min. This mixture was then titrated by a
liquid was clear. The filtrate was then refluxed standard 0.25 M NaOH solution, using
with 240 mL of 5% sodium hypochlorite phenolphthalein as indicator. The percentage of
(NaOCl) at 80°C for 18 min for the bleaching acetyl groups (%AG) was calculated by
process. After another washing and filtration following equation:
step, it then was hydrolyzed with 122 mL of 2 M %AG = {[(Vbi + Vbt) * µb – (Va * µa)] * M *
HCl at room temperature for 30 min under 100}/mac
continuous stirring. It was repeatedly washed Where:
with distilled water until pH sevenis achieved. Vbi; volume of NaOH added to the system (L)
The cellulose was dried in an oven at 50°C for Vbt: volume of NaOH spent in titration (L)
24h. The mass of dried cellulose was recorded to µb: NaOH concentration (M)
Va: volume of HCl added to the system (L) hemicellulose [9]. Since some of other fibers
µa: HCl concentration (M) have degraded, the cellulose content increased.
M: molar weight of acetyl group (43 g/mol) The yield of the extraction process was around
mac: weight of cellulose acetate sample (g) 43%. The MCC was made by hydrolysis of
cellulose on its glycosidic bond [16].
Meanwhile, the degree of substitution was
calculated using following equation from
FT-IR spectra of MCC and cellulose acetate
Elomaa et al. [13].
based Sago ‘hampas’
DS = 162* %AG/[4300– (42 * %AG)]
Figure 1 showed FT-IR spectrum of cellulose
acetate produced by various volume of acetic
RESULTS AND DISSCUSION
anhydride.There are cellulose-specific groups in
Microcrystalline Cellulose based Sago
standard cellulose (-OH, -CH2, -O- groups) that
‘hampas’
appear repeatedly. The -OH group appears at
Characteristics of dried sago ‘hampas’ and
wave number 3348,42 cm-1, while wave number
microcrystalline cellulose based sago ‘hampas’
2900,94 cm-1 shows vibration CH2 which is the
can be seen from Table 1.
main frame builder of cellulose compound
reinforced with vibration at wave number
Table 1. Characteristics of sago ‘hampas’ and
2366,59 cm-1. The -O- group that assembles
microcrystalline cellulose based sago ‘hampas’
cellulose appears at wave numbers 1319.31 and
1373.32 cm-1 [25].The absence of vibration in
Water content Cellulose the wave number1509-1609 cm-1 and 1700-1740
Yield (%)
(% db) content (%) cm-1 on the FT-IR cellulose spectral profile of
Sago MCC showed no presence of lignin and
16.38±0.84 35.47±0.17 -
waste hemicellulose compounds in the MCC based
MCC 11.29±0.08 58.83±0.12 42.91±1.12 sago ‘hampas’[26]. From Fig 1, It can be seen
that there isan alterationof intensity band at
From the result, it shows that sago ‘hampas’ still ~3400 cm-1. On the control, the intensity is
has relatively high cellulose content, around around 4.3%T, while the cellulose acetate had
35%. The remaining composition of that could the intensity of peak around 12.9%T. This
be the starch, hemicellulose, and lignin. Sago conversion means that there is a modification of
waste or hampascontains 58% starch, 23% hydroxyl groups to acetyl groups [12]. On
cellulose, 9.2% hemicellulose, and 4% lignin Figure 1, it was also shown an adsorption peak
[14]. According to Chew and Shim [15], at 1242 cm-1 which assigned for C-O stretching
microscopic examination showed that a large of acetyl group, which wasn’t observed on MCC
amount of starch granules were trapped within sago waste and treatment 0 ml acetic anhydride
the lignocellulosic matrix of sago waste. The [17]. The strong intensity band presented at
relatively high cellulose content on this 1751 cm-1of acetic anhydride addition is
experiment most likely caused by soaking as assigned to symmetric carbonyl group (C=O) of
pretreatment which was done before the acetyl group [18]. This figure confirm that there
cellulose extraction. Some amount of starch wasn’t acetic acid and acetate anhydride residue
which is a soluble carbohydrate were already by the absence of band at 1760-1840 cm-1 [19].
dissolved in the soaking process, making the There is a noticable peak at 902 cm-1 of
sago waste cellulose more concentrated. cellulose acetate which indicated the
After the cellulose extraction, the cellulose degradation of cellulose due to acetylation
content increased to approximately 59%. The process [20].
alkali treatment solubilized lignin and
Fig 1. FT-IR spectra of cellulose standard (A); MCC sago ‘hampas’ (B); cellulose acetate treatment 0 ml acetate
anhydride (C); 30 ml acetate anhydride (D); 60 ml acetate anhydride (E); 66 ml acetate anhydride (F)
Water content of the cellulose acetate appeared OH groups to the environment as a result from
to increase with the addition of acetic acetyl groups substitution. Those OH groups
anhydride. This might be caused by release of formed free water molecules and thus increased