scholarly journals Production of Methyl ester from Coconut Oil using Heterogeneous K/Al2O3 under Microwave Irradiation

2020 ◽  
Vol 5 (2) ◽  
pp. 23-29
Author(s):  
Andi Suryanto ◽  
Ummu Kalsum ◽  
Lailatul Qadariya ◽  
Mahfud Mahfud

Methyl esters derived from coconut oil are very interesting to study because they contain free fatty acids with a medium carbon chain structure (C12-C14), so most methyl esters (70%) can be bio-kerosene and the rest can be biodiesel. The process of preparing methyl ester by reaction of Trans-esterification triglyceride generally using a homogeneous KOH catalyst but this process requires a long catalyst separation process through washing and drying process. The use of heterogeneous catalysts in the production of methyl esters can remove the washing and drying processes, but trans-esterification reactions with heterogeneous catalysts require severe conditions (high pressure and high temperature), whereas at low temperatures and atmospheric conditions, the methyl ester yield is relatively low. Using microwave-irradiated trans-esterification reactions with heterogeneous catalysts, it is expected to be much faster and can obtained higher yields. Therefore, in this study we prepare a heterogeneous catalyst K/Al2O3 using solution KOH that impregnated in catalyst support Al2O3, and catalyst obtained are caracterized by XRD, BET dan SEM. Our objective was to compare the yield of methyl esters obtained through the trans-esterification process of coconut oil assisted by microwave using a heterogeneous K / Al2O3 catalyst with yield obtained using a homogeneous KOH catalyst. Experimental equipment consists of a batch reactor placed in a microwave oven equipped with a condenser, agitator and temperature controller. The batch process was carried out at atmospheric pressure with variation of K/Al2O3 catalyst concentration (0.5, 1.0, 1.5, 2.0, 2.5%) and microwave power (100, 264 and 400 W). In general, the process of producing methyl esters by heterogeneous catalysts will get three layers, wherein the first layer is the product of methyl ester, the second layer is glycerol and the third layer is the catalyst. The experimental results show that the methyl ester yield increases with increasing of microwave power, catalyst concentration and reaction time. The results obtained with K /Al2O3 catalysts are generally slightly lower than those obtained using a homogeneous KOH catalyst. However, the yield of methyl esters obtained by the K / Al2O3 heterogeneous catalyst process are relatively easy to separate rather than using a homogeneous KOH catalyst.

Jurnal Kimia ◽  
2019 ◽  
Vol 13 (1) ◽  
pp. 1 ◽  
Author(s):  
N. K. D. Astuti ◽  
I N. Simpen ◽  
I W. Suarsa

The CaO heterogeneous catalysts can be prepared by CaCO3 calcination process, with one source of CaCO3 being a crab shell from seafood waste. The preparation of the heterogeneous catalyst was successfully carried out by modification with KOH using a wet impregnation method at 800oC for 5 hours. The purpose of this research is to determine the physical and chemical characteristics of heterogeneous catalyst of K2O-modified crab shell and to examine the heterogeneous catalyst of K2O-modified shells in converting rubber seed oil into biodiesel. The results showed that the lowest basic alkalinity possessed without modified catalyst (1.0428 mmol g-1) and the highest alkali possessed potassium-modified catalyst (1.8314 mmol g-1). Characterization of specific surface area of ??crab shells without and with modified K2O were relatively the same. The surface morphology of the catalyst without and K2O modified was uniform. The catalyst examination results for conversion of rubber seed oil (Hevea brasiliensis) to biodiesel, the optimum catalyst concentration of 3% and the molar ratio of oil:methanol of 1:9 capable converting to biodiesel with the yield of 91.05%. The content of biodiesel were stearic methyl ester, linoleic methyl ester, linolenic methyl ester, and palmitic methyl ester.


2013 ◽  
Vol 13 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Kamisah D. Pandiangan ◽  
Wasinton Simanjuntak

In this study, transesterification of coconut oil with dimethyl carbonate (DMC) for preparing biodiesel has been studied using TiO2/SiO2 as heterogeneous catalyst, with the main purpose to investigate the effect of molar ratio of DMC to oil. The product was analyzed by GC-MS to identify the fatty acid methyl esters (FAMEs) composting the biodiesel. The significant role of the DMC to oil ratio was observed in this study, in which the oil conversion was found to increase with increasing molar ratio of DMC : Oil, with the highest percent of conversion of 88.44%. The GC-MS analysis revealed the presence of methyl esters in accordance with the composition of coconut oil commonly reported. Formation of FAMEs was verified by 1H-NMR spectroscopic analysis, which also suggested that some of the fatty acids remain unconverted into biodiesel. The biodiesel produced was found to have kinematic viscosity of 2.4 mm2/S at 40 °C, flash point of 103 °C, and cetane number of 54.


2019 ◽  
Author(s):  
Iman Setiono ◽  
Murni . ◽  
Rtd Wisnu Broto

Fossil energy is a limited source of primary energy, various efforts have been made to find alternative fuels that are renewable. Vegetable oil is one of the plants that can be a source of energy, but must be converted into other forms, namely alkyl esters (biodiesel). Biodiesel is a diesel fuel substitute that can be used as a raw material for making or mixing in transportation fuels. In this study, biodiesel will be produced using an esterification-transesterification process with NiZn/Al2O3catalyst. Process variables include:temperaturesof90,120,150and180oC.theratiooffeedmethanol:palmoilata ratio of 1: 15. The concentration of NiZn/Al2o3 catalyst was varied at 1, 1.5, 2, and 2.5%. NiZn/Al2O3 catalyst was synthesized using wet impregnation method with loading of nickel and Zink at 5% wt. The catalyst will be analyzed using XRD and SEM analysis. Nickel and Zink metals in the NiZn/Al2O3catalyst catalyst have been dispersed on the surface of Al2O3. Al2O3 calcination before the impregnation process produced NiZn /Al2O3 catalyst with a crystallinity of 62,99%. The results of this study concluded that the biodiesel produced increased with increasing catalyst concentration, temperature, reaction in the esterification-transesterification process where at a temperature of 90oC and catalyst concentration 0.015 g catalyst / gr feed and reaction time of 1.5 hours obtained biodiesel yield of 35.8%, at temperature of 90oC and at a temperature of 180oC and catalyst concentration of 0.01 g catalyst/gr feed obtained biodiesel yield of 48.3%. Biodiesel was analyzed by GCMS to measure the composition of methyl esters and test the properties of biodiesel according to ASTM standards.


Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1407
Author(s):  
Martinique S. Nunes ◽  
Diana M. Gomes ◽  
Ana C. Gomes ◽  
Patrícia Neves ◽  
Ricardo F. Mendes ◽  
...  

There is a considerable practical interest in discovering new ways to obtain organomolybdenum heterogeneous catalysts for olefin epoxidation that are easier to recover and reuse and display enhanced productivity. In this study, the complex salt (H2pytz)[MoO2Cl2(pytz)] (1) (Hpytz = 5-(2-pyridyl)tetrazole) has been prepared, structurally characterized, and employed as a precursor for the hydrolysis-based synthesis of a microcrystalline molybdenum oxide/organic hybrid material formulated as [MoO3(Hpytz)] (2). In addition to single-crystal X-ray diffraction (for 1), compounds 1 and 2 were characterized by FT-IR and Raman spectroscopies, solid-state 13C{1H} cross-polarization (CP) magic-angle spinning (MAS) NMR, and scanning electron microscopy (SEM). Compounds 1 and 2 were evaluated as olefin epoxidation catalysts using the model reaction of cis-cyclooctene (Cy8) with tert-butyl hydroperoxide (TBHP), at 70 °C, which gave 100% epoxide selectivity up to 100% conversion. While 1 behaved as a homogeneous catalyst, hybrid 2 behaved as a heterogeneous catalyst and could be recovered for recycling without showing structural degradation or loss of catalytic performance over consecutive reaction cycles. The substrate scope was broadened to monoterpene DL-limonene (Lim) and biobased unsaturated fatty acid methyl esters, methyl oleate (MeOle), and methyl linoleate (MeLin), which gave predominantly epoxide products.


Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1405
Author(s):  
José María Encinar ◽  
Juan Félix González ◽  
Gloria Martínez ◽  
Sergio Nogales-Delgado

The use of heterogeneous catalysts to produce fatty acid methyl esters (FAME) through transesterification with methanol might contribute to both green chemistry and a circular economy, as the process can be simplified, not requiring additional stages to recover the catalyst once the reaction takes place. For this purpose, different catalysts are used, including a wide range of possibilities. In this research the use of NaNO3/SiAl as a heterogeneous catalyst for FAME production through transesterification of rapeseed oil with methanol is considered. A thorough characterization of the catalyst (including XDR and XPS analysis, SEM microscopy, lixiviation and reusability tests, among others), specific optimization of transesterification by using the final catalyst (considering catalyst amount, stirring rate, methanol/oil ratio, and temperature), and quality determination of the final biodiesel (following the UNE-EN 14214 standard) were carried out. In conclusion, 20 mmolNa·gsupport−1 (that is, NaNO3/SiAl 20/1) offered the best results, with a high activity (exceeding 99% w/w of FAMEs) without requiring higher impregnation amounts. The best chemical conditions for this heterogeneous catalyst were 5% w/w catalyst, 700 rpm, 9:1 methanol/oil ratio, and 65 °C, obtaining Ea = 73.3 kJ·mol−1 and a high-quality biodiesel, similar to those obtained through homogeneous catalysis. Consequently, this catalyst could be a suitable precursor for FAME production.


PHARMACON ◽  
2019 ◽  
Vol 8 (4) ◽  
pp. 904
Author(s):  
Meiga Paendong ◽  
Hanny F. Sangian ◽  
Maria D. Bobanto

ABSTRACT             The purpose of this research is to prepare a blended fuel of biodiesel, diesel and ethanol in stable emulsion. Biodiesel which is mixed with diesel and ethanol in certain compositions was conducted manually. The first step was to prepare ethanol from fermented palm sap and then the ethanol and water were distililed using a reflux separator. The ethanol obtained was with purity 94-96%, while 97% ethanol was produced by lime absorbsion. The next step was the mixing process between ethanol, biodiesel and ethanol, biodiesel, and diesel. Ethanol was poured into a measuring flask with a volume of 7 ml and then biodiesel was added until they formed a stable emulsion solution. The ethanol and diesel were mixed and the biodiesel was added gradually while shaken slowly forming a stable emulsion. The results showed that the composition of biodiesel, ethanol, and water with 96% ethanol were 78.76, 20.42 and 0.81% (v/v), where methyl esters were obtained from palm oil using subcritical techniques. Meanwhile, biodiesel from coconut oil with the same technique, the composition of the three components was 75.13% biodiesel, 23.90% ethanol and 0.95% air. Keywords: Biodiesel, Ethanol, Diesel, Palm Tree (Arenga pinnata SP).                                             ABSTRAKTujuan penelitian ini adalah membuat bahan bakar campuran larutan emulsi stabil dengan mencampurkan biodiesel, diesel dan etanol. Biodiesel  yang dicampur dengan diesel dan etanol pada komposisi tertentu dilakukan secara manual. Tahapan yang pertama yaitu pembuatan etanol dari nira aren yang sudah terfermentasi dan kemudian dilakukan proses destilasi etanol untuk mendapat kemurnian 94-96%, sementara untuk etanol 97 % didapat dengan cara absorsi menggunakan lime. Tahapan berikutnya yaitu proses pencampuran dilakukan dengan menggunakan etanol dengan kemurnian 94%-97%. Etanol dituangkan ke dalam gelas ukur dengan volume 7 ml dan etanol konsentrasi 96% dicampur secara perlahan hingga membentuk larutan emulsi stabil. Hasil menunjukan bahwa komposisi biodiesel, etanol, dan air dengan kosentrasi etanol 96% adalah 78.76, 20.42 dan 0.81 % (v/v) yang mana methyl ester diturunkan dari minyak sawit dengan menggunakan teknik subkritis. Sementara, biodiesel dari minyak kelapa dengan teknik yang sama, komposisi ketiga komponen adalah  75.13 % biodiesel, 23.90 % etanol dan 0.95% air. Kata kunci: Biodiesel, Etanol, Diesel, Pohon Aren (Arenga pinnata SP)


KOVALEN ◽  
2020 ◽  
Vol 6 (3) ◽  
pp. 206-211
Author(s):  
Sumarni ◽  
Erwin Abdul Rahim ◽  
Ni Ketut Sumarni ◽  
Ruslan ◽  
Hardi Ys. ◽  
...  

Research on the manufacture of methyl esters from avocado seeds (Parsea americana Mill) with eugenol-based catalysts has been conducted. The aim is to determine the catalyst concentration used to produce methyl esters with the highest rendement and determine the composition of fatty acid methyl ester in avocado seeds. This study was used variations in concentrations of 0.25%, 1%, 1.75%, 2.25%, and 3%. The results of this study showed that the best concentration is 2.25% with the calculation of the results of 24.8% methyl esters in avocado seeds, namely lignoceric and octadecenoic acid methyl ester. Keywords: Avocado seeds, fatty acid methyl esters


Author(s):  
Nurul Aina Nasriqah Binti Ma’arof ◽  
Noor Hindryawati ◽  
Siti Norhafiza Mohd Khazaai ◽  
Prakash Bhuyar ◽  
Mohd Hasbi Ab. Rahim ◽  
...  

Biodiesel, an environmentally friendly biomass-based fuel, is gaining popularity globally as a cost-effective way to meet rising fuel demand. However, the high cost of raw materials and catalysts continues to drive up biodiesel production. An alternative feedstock with a heterogeneously catalyzed reaction could be the most cost-effective way to stabilize industrial biodiesel growth. Understanding these issues led to the idea of using waste palm oil as a feedstock for biodiesel production. While using waste materials as feedstock for biodiesel is an elegant solution, converting high free fatty acids (FFA) directly into methyl esters has some drawbacks. High FFA processes (acid esterification, then base transesterification) are costly. The commercial processes currently use a homogeneous system with sulfuric acid to catalyze both esterification and transesterification. However, heterogeneous solid acid catalysts are preferred over hazardous mineral acids for high FFA esterification because they are less corrosive, produce less waste, and are easier to separate from reactants and products by filtration, recovery, and reusability. Heterogeneous acid catalysts can also simultaneously catalyze transesterification and esterification reactions. Thus, new waste-based support for heterogeneous catalysts (solid acid catalysts) is required to convert waste oils into biodiesel.


2016 ◽  
Vol 864 ◽  
pp. 77-80
Author(s):  
Ni Made Suaniti ◽  
I. Wayan Bandem Adnyana ◽  
Manuntun Manurung ◽  
Nadya Hartasiwi

This Lauric acid is the most abundant fat in coconut oil, which can undergo an esterification and trans-esterification reactions to form methyl laurate. The aim of this study was to characterize the results obtained from lauric acid esterification and tran-esterification VCO enzymatic produce methyl esters with a distinctive odor ester. VCO enzymatic_methanol esterification (9: 1) with phosphoric acid catalyst and tran-esterification results esterification_methanol (1: 3) with KOH catalyst with varies time were 0.5; 1; 1.5; and 2 hours with the percentage obtained FAME row is 73.97; 78.09; 91.75; and 89.83%. Characterizations of methyl laurate were (1) density: 857.97; 857.97; 859.90; and 860.00 kg/m3, (2) % FFA: 0.16; 0.12; 0.09; 0.07% and acid value: 0.44; 0.32; 0.24; 0.14 mg-KOH/g sample. (3) Functional groups showed similarities value with the methyl laurate standard by the FT-IR spectrophotometer, the presence of ester compounds such as C = O; C-O; C-H; CH3; and RCOOR.


2018 ◽  
Vol 34 (6) ◽  
pp. 3030-3036 ◽  
Author(s):  
Zuhrina Masyithah ◽  
Dinar Rajagukguk ◽  
Samuel Oktavianus Purba ◽  
Armansyah Ginting

Coco ethanolamide obtained from the amidation of Fatty acid methyl ester (FAME) from coconut oil with monoethanolamine using zirconium (IV) chloride and tert-amyl alcohol was observed in this study. Several effective parameters were evaluated in term of catalyst concentration (5-9% w/wFAME), reaction temperature (80-100oC) and stirring speed (200-400 rpm). Response Surface Methodology (RSM) was used to optimize and to observe the interaction effects of the three variables on the FAME conversion. The capability of the process was measured from the number of FAME converted to coco ethanolamide. In the range of parameters evaluated, the conversion increase by increasing the catalyst concentration up to 9% (w/wFAME), but decreases after the optimum value. At the optimal condition, the model predicts a maximum FAME conversion of 86.27%, mainly due to a strong interaction between catalyst concentration and stirring speed.


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