scholarly journals Transesterification of Waste Cooking Oil Using NH2/MCM-41 Base Catalyst: Effect of Methanol/Oil Mole Ratio and Catalyst/Oil Weight Ratio towards Conversion of Ester

2018 ◽  
Vol 30 (5) ◽  
pp. 953-957 ◽  
Author(s):  
Triyono ◽  
Wega Trisunaryanti ◽  
Adriana Dwi Putri ◽  
Ayyik Lutfiana ◽  
Kumala Dewi
2017 ◽  
Vol 17 (3) ◽  
pp. 509 ◽  
Author(s):  
Ida Bagus Putra Mahardika ◽  
Wega Trisunaryanti ◽  
Triyono Triyono ◽  
Dwi Putra Wijaya ◽  
Kumala Dewi

Transesterification of waste cooking oil using CaO/MCM-41 synthesized from Lapindo mud by the sonochemical method has been carried out. The silica was separated from the mud by reflux method used 6 M HCl and 6 M NaOH. The silica was then analyzed by XRF and used as silica source in MCM-41 synthesis. The synthesis of MCM-41 was carried out by the sonochemical method, then analyzed by XRD, Infrared spectrophotometer, SAA, and TEM. The Ca2+ was loaded onto the MCM-41 by wet impregnation method under variation of the Ca2+ content of 1.15, 1.29, 2.39, and 3.25 wt.% analyzed by ICP produced CaO(1), CaO(2), CaO(3), and CaO(4)/MCM-41 catalyst respectively. Transesterification of used cooking oil was carried out under methanol/oil mole ratio of 15/1, the temperature of 55, 65 and 75 °C, and catalyst/oil weight ratio of 5/100, 10/100 and 15/100 for 2 h by reflux method. The XRD analysis of the MCM-41 showed a characteristic peak at 2θ = 2-5°. The MCM-41 has a specific surface area of 1290 m2/g and pore diameter of 3.4 nm. The TEM images of MCM-41 showed ordered pore distribution with a hexagonal shape. The highest conversion of methyl ester was 78.17 wt.% obtained under the reaction conditions at 65 °C and catalyst/oil weight ratio of 15/100 using the CaO(4)/MCM-41. The lifetime CaO(4)/MCM-41 catalyst was 9.8 h.


2007 ◽  
Vol 50 (2) ◽  
pp. 79-86 ◽  
Author(s):  
Masato Kouzu ◽  
Shinya Yamanaka ◽  
Takekazu Kasuno ◽  
Masahiko Tajika ◽  
Yoichi Aihara ◽  
...  

2013 ◽  
Vol 803 ◽  
pp. 17-20 ◽  
Author(s):  
Ming Gao ◽  
Cui Bao Guo ◽  
Xing Lin

Biodiesel is a renewable, biodegradable, and nontoxic fuel. At present, biodiesel is primarily produced in batch reactors in which the required energy is provided by heating accompanied by mechanical mixing. Alternatively, ultrasonic processing is an effective way to attain required mixing while providing the necessary activation energy. Biodiesel was synthesized by waste cooking oil using ultrasonication and alkali-acid catalysis method. Its structure was characterized by gas chromatograph, and the effects of various factors on transesterification rate were studied. The results show that a biodiesel yield in excess of 91% can be achieved in 30 min, at the 30Hz amplitude level, methanol/oil weight ratio of 1.3, 2% of alkaline, reaction temperature of 40-50 °C..


2021 ◽  
Author(s):  
Olayomi Abiodun Falowo ◽  
Babatunde Oladipo ◽  
Abiola Ezekiel Taiwo ◽  
Tomiwa Ayomiposi Olaiya ◽  
Oluwaseun Oyekola ◽  
...  

Abstract Economical feedstocks such as agricultural wastes, food wastes, and waste cooking oil were used for biodiesel production to expand their application. Thus, a solid base catalyst was synthesized from a mixture of ripe and unripe plantain peels at a calcination temperature of 500 oC for 4 h. The catalyst was characterized using Scanning Electron Microscope (SEM), X-ray Diffraction (XRD) analysis, Fourier Transform Infrared (FT-IR) spectroscopy, Energy dispersive X-ray (EDX) analysis, and Brunauer-Emmett-Teller (BET) method. The waste cooking oil (WCO) used in this study was first pretreated with 3% (v/v) of H2SO4 via esterification reaction due to its high acid value. The esterified WCO was converted to biodiesel via transesterification reaction, and the process was then modeled and optimized using Taguchi L9 orthogonal array design method considering reaction temperature, reaction time, catalyst amount, and methanol/WCO molar ratio as the input variables. Based on the results, the synthesized catalyst predominantly contained potassium phases with 45.16 wt.%. The morphology of the catalyst revealed a crystalline mesoporous nanocomposite. At the end of WCO esterification, the acidity of the oil decreased from 5 to 1 mg KOH/g. The optimal conditions established for the transesterification process were catalyst amount of 0.5 wt.%, methanol/WCO molar ratio of 6:1, reaction temperature of 45 oC, and reaction time of 45 min with a corresponding biodiesel yield of 97.96 wt.%. The quality of the biodiesel produced satisfied the specifications (ASTM D6751 and EN 14241) recommended for biodiesel fuels. Hence, a blend of ripe and unripe plantain peels could serve as an efficient heterogeneous base catalyst in producing biodiesel from WCO.


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