THE BIODIESEL PROCESSING FROM OIL OF YELLOWFIN TUNA [Thunnus albacares (Bonnaterre, 1788)] OFFAL USING ACID CATALYST

2016 ◽  
Vol 78 (4-2) ◽  
Author(s):  
Latif Sahubawa ◽  
Juju Junengsih ◽  
Ustadi Ustadi

Biodiesel is one of the alternative fuels to meet the need of the diesel fuel in Indonesia. One of potential animal oil/fat to be utilized as biodiesel raw material is offal from yellowfin tuna. The objective of the study is to know the free fatty acid (FFA) levels of raw material, influence of the H2SO4 concentration as catalyst on biodiesel conversion, composition of the main Fatty acid compounds from biodiesel, and physical characteristics of biodiesel through esterification and transesterification reaction. In transesterification phase, the variabel is H2SO4 concentration 1.25 %, 1.50% and 1.75 % at 60 °C and 65 °C with oil to methanol molar ratio of 1:9. Based on experiment results, the know  that: FFA content from oli of yellowfin tuna offal amounted to 2.33 %, the largest conversion of methyl ester from spectra of H-NMR, FT-IR, GC-MS and ASTM was produced from the treatment with 1.50 % H2SO4 at 65 °C, with an average yield of 89.09 % and the conversion value of methyl ester was 52.63 %. The main compounds of Fatty acids that formed biodiesel were palmatic acid (43.64 %) and oleic acid (32.08 %). The physical characteristics of biodiesel according to the national standards of Indonesia (NSI) were specific density of 0.8637 60/60 °F g mL–1kinematic viscosity of 2.555 mm2 s–1, pour point is -3 °C and cloud point of 25 °C, while flash point of 25 °C and water content of 0.20 % was not consistent with the SNI. 

2013 ◽  
Vol 2 (3) ◽  
pp. 44-50
Author(s):  
Bella Simbolon ◽  
Kartini Pakpahan ◽  
Siswarni MZ

This research aims to exploit the coffee seed oil as raw material for biodiesel by esterification process, then followed by transesterification process and studied the influence of variations in the weight ratio of solvent: ground coffee beans in the coffee bean oil extraction process. The methodologies of this researchare conducted on the process of preparation of raw materials, extraction, and testing phase.  Extraction is done with a variety of types of solvent n-hexane (C6H14) and toluene (C7H8 (C6H5CH3)) and a variety of solvents through a ratio of 1:5, 1:6, 1:7 and 1:8 against the mass of each run, which is 40 gram. Another variable is still 2 hours extraction time and temperature solvent extraction with n-hexane (C6H14) (boiling point 690C) is 70-75 0c and the solvent toluene (C7H8 (C6H5CH3))(boiling point 1100C) is 110-1150C. Testing phase is done bythe use of coffee oil esterification process in the molar ratio of methanol: free fatty acid catalyst H2SO4 = 3:1 with 1% v / v for 1hour with stirring 600 rpm and transesterification process at a molar ratio of methanol: oil = 9:1 coffee with 1.75% NaOH catalyst for 2 hours with stirring 600 rpm. Esterification process as conducted preliminary due to high levels of free fatty acids coffeeoils, which is 22.2%. Extraction results include the maximum yield of the coffee oils  17.73% in toluene weight ratio: coffee powder= 6:1, and coffee oil data in the form of the density 93.75 g / ml, viscosity 59.326 cP and fatty acid composition of the highest linoleic acid 40.8765% and palmitic acid 37.4492%. The results of esterification and transesterification obtained by the methyl ester equal to 39.63% with density 0.915 g / ml, 22.5498 cSt kinematic viscosity and flash point 130 0C.


2018 ◽  
Vol 156 ◽  
pp. 03002
Author(s):  
Iwan Ridwan ◽  
Mukhtar Ghazali ◽  
Adi Kusmayadi ◽  
Resza Diwansyah Putra ◽  
Nina Marlina ◽  
...  

The oleic acid solubility in methanol is low due to two phase separation, and this causes a slow reaction time in biodiesel production. Tetrahydrofuran as co-solvent can decrease the interfacial surface tension between methanol and oleic acid. The objective of this study was to investigate the effect of co-solvent, methanol to oleic acid molar ratio, catalyst amount, and temperature of the reaction to the free fatty acid conversion. Oleic acid esterification was conducted by mixing oleic acid, methanol, tetrahydrofuran and Amberlyst 15 as a solid acid catalyst in a batch reactor. The Amberlyst 15 used had an exchange capacity of 2.57 meq/g. Significant free fatty acid conversion increments occur on biodiesel production using co-solvent compared without co-solvent. The highest free fatty acid conversion was obtained over methanol to the oleic acid molar ratio of 25:1, catalyst use of 10%, the co-solvent concentration of 8%, and a reaction temperature of 60°C. The highest FFA conversion was found at 28.6 %, and the steady state was reached after 60 minutes. In addition, the use of Amberlyst 15 oleic acid esterification shows an excellent performance as a solid acid catalyst. Catalytic activity was maintained after 4 times repeated use and reduced slightly in the fifth use.


2014 ◽  
Vol 692 ◽  
pp. 133-138
Author(s):  
Athitan Timyamprasert ◽  
Vittaya Punsuvon ◽  
Kasem Chunkao ◽  
Juan L. Silva ◽  
Tae Jo Kim

The aim of this research was to develop a two-step technique to prepare biodiesel from waste palm oil (WPO) with high free fatty acid content. The developed process consists of esterification and transesterification steps. Response surface methodology (RSM) was applied for investigating the experimental design for esterification step. Design of experiment was performed by application of 5-levels-3-factors central composite design in order to study the optimum condition for decreasing FFA in WPO. The WPO with low FFA was further experimented in transesterification step to obtain fatty acid methyl ester (FAME). The investigated results showed that the WPO containing 48.62%wt of high FFA. The optimum condition of esterification step was 28 moles of methanol to FFA in WPO molar ratio, 5.5% sulfuric acid concentration in 90 min of reaction time and 60 °C of reaction temperature. After transesterification step, WPO biodiesel gave methyl ester content at 84.05% according to EN 14103 method. The properties of WPO methyl ester meet the standards of Thailand community biodiesel that can be used as fuel in agricultural machine.


2016 ◽  
Vol 723 ◽  
pp. 610-615 ◽  
Author(s):  
Natta Pimngern ◽  
Vittaya Punsuvon

Crude coconut oil with high free fatty acid (FFA) content was used as a raw material to produce biodiesel. In this work, the esterification followed by transesterification of crude coconut oil with methanol is studied. The response surface methodology (RSM) with 5-level-3-factor central composite design (CCD) was applied to study the effect of different factors on the FFA content of esterification and the percentage of fatty acid methyl ester (FAME) conversion of transesterification. The FAME conversion was detected by proton magnetic resonance (1H-NMR) spectrometer. As a result, the optimum conditions for esterification were 6:1 of methanol-to-oil molar ratio, 0.75wt% of sulfuric acid (H2SO4) concentration and 90 min of reaction time. The optimum conditions for transesterification were 8.23:1 of methanol-to-oil molar ratio, 0.75wt% of sodium hydroxide (NaOH) concentration and 80 min of reaction time. Quadratic model equations were obtained describing the relationships between dependents and independent variables to minimize the FFA content and maximize the FAME conversion. Fuel properties of the crude coconut oil biodiesel were also examined followed ASTM and EN standards. The results showed that all properties met well with both standards.


Author(s):  
Manish Kumar Kanth ◽  
Chandrawati Jee ◽  
Anit Kumar ◽  
Abhijeet Kashyap ◽  
Rupam Kumari ◽  
...  

Today’s developmental world needs large amount of energy. Due to the limited fossil fuel source, there is need of some alternate fuel sources among which biodiesel from vegetable oil widely practiced. There is an increasing interest in India to search for suitable low cost alternative fuels that are Eco friendly. Biodiesel is a renewable, biodegradable and non toxic fuel. In this paper an attempt has been made to study and compare the oil percentage and Fatty acid methyl ester (FAME) components of three non edible oil seed plants abundantly found in Bihar, India. Oil from the seed kernel was extracted by solvent extraction technique through Soxhlet apparatus using n-hexane as solvent. Percentage oil content for Jetropha, Mahua and Castor are found around 76 %, 41% and 33% respectively. Further extracted oil were analysed by GC-MS for their FAME components. Palmitic, linoleic, oleic are most common fatty acid found among three.


2021 ◽  
Vol 16 (3) ◽  
pp. 601-622
Author(s):  
Nur Nazlina Saimon ◽  
Mazura Jusoh ◽  
Norzita Ngadi ◽  
Zaki Yamani Zakaria

Microwave-heating method for catalyst preparation has been utilized recently due to its shorter operation time compared to the conventional method. Glucose, a renewable carbon source can be partially carbonized and sulfonated via microwave heating which could result in highly potential heterogeneous carbon-based acid catalyst. In this study, the impacts of the carbonization and sulfonation parameters during the catalyst preparation were investigated. Catalysts prepared were characterized using Fourier Transform Infrared Spectroscopy (FTIR), Field Emission Scanning Electron Microscopy (FESEM), X-Ray Diffraction (XRD), Brunauer-Emmet-Teller (BET), and Temperature Programmed Desorption–Ammonia (TPD-NH3). Analysis of the carbonization screening process discovered that the best incomplete carbonized glucose (ICG) prepared was at 20 minutes, 20 g of D(+)-glucose with medium microwave power level (400W) which exhibited the highest percentage yield (91.41%) of fatty acid methyl ester (FAME). The total surface area and acid site density obtained were 16.94 m2/g and 25.65 mmol/g, respectively. Regeneration test was further carried out and succeeded to achieve 6 cycles. The highest turnover frequency (TOF) of the sulfonated catalyst was methyl palmitate, 25.214´10−3 s−1 compared to other component of the methyl ester. Kinetic study was developed throughout the esterification process and activation energy from the forward and reverse reaction was 3.36 kJ/mol and 11.96 kJ/mol, respectively. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1029 ◽  
Author(s):  
Umer Rashid ◽  
Soroush Soltani ◽  
Thomas Shean Yaw Choong ◽  
Imededdine Arbi Nehdi ◽  
Junaid Ahmad ◽  
...  

A palm waste kernel shell biomass was converted into bio-based sulphonated activated carbon and further used for preparation of a sulphated zirconium-doped activated catalyst (Zr-AC-HSO3) by wet impregnation method. The structural, physicochemical, morphological, textural, and thermal characteristics of the synthesized Zr-AC-HSO3 catalyst were characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) surface area analysis, temperature-programmed desorption of ammonia (TPD-NH3), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). The catalytic activity of the 20 wt% Zr-AC-HSO3 catalyst was further evaluated for esterification of palm fatty acid distillate (PFAD). This study achieved a maximum fatty acid methyl ester (FAME) yield of 94.3% and free fatty acid (FFA) conversion of 96.1% via the esterification over 20 wt% Zr-AC-HSO3 using 3 wt% catalyst concentration, 15:1 methanol:PFAD molar ratio at 75 °C for 3 h. The experiments to test for reusability showed that the spent catalyst was stable for five successive reaction cycles, with a FFA conversion of 80% in the fifth cycle, without additional treatment. The critical fuel features of the synthesized PFAD methyl ester were determined and were within the range of EN14214 and ASTM D6751 standards.


2015 ◽  
Vol 81 ◽  
pp. 347-354 ◽  
Author(s):  
Ibrahim M. Lokman ◽  
Umer Rashid ◽  
Yun Hin Taufiq-Yap ◽  
Robiah Yunus

2011 ◽  
Vol 11 (1) ◽  
pp. 41 ◽  
Author(s):  
Susan A Roces ◽  
Raymond Tan ◽  
Francisco Jose T Da Cruz ◽  
Shuren C Gong ◽  
Rison K Veracruz

Studies were carried out on the transesterification, also called methanolysis, of oil from the Jatropha curcas L. with methanol using conventional heating for the production of biodiesel. All reactions were carried out in a batch-stirred reactor and in the subsequent separation and purification stages. The high free-fatty acid (FFA) level of Jatropha oil was reduced to less than 1% by a two-step process. The first step was carried out with 12% w/w methanol-to-oil ratio in the presence of 1% w/w HCl as acid catalyst in a 2h reaction at 343K. The second step was carried out with variable parameters: temperatures at 318K and 333K, initial catalyst concentrations at 0.5% and 1.5%, methanol:oil molar ratios at 4:1 and 6:1, and reaction times at 1h and 2h. Gas chromatography analysis was used to determine the fatty acid profile of crude Jatropha oil. Methanolysis of Jatropha oil used the catalysts NaOH and KOH. The high FFA level of Jatropha oil was reduced from 6.1% to 0.7% after the first step process. The highest yield of fatty acid methyl esters (FAME), however, was achieved at 92.7% in 2h at 4:1 methanol:oil molar ratio, 1.5% w/w KOH, and 333K reaction temperature. This method produced biodiesel that met ASTM’s biodiesel standards. Results showed a density of 0.8g/ml that is within 0.86–0.9kg/l standard range and a kinematic viscosity of about 4.1cSt that is within 2–4.5cSt standard range. The flash point of the biodiesel samples fell between 169oC and 179oC while the cloud point averaged at 6oC.


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