Synthesis Of Methyl Esters Research Articles

Catalytic Fatty Acid Methyl Esters (FAMEs) Synthesis Using Lepidium aucheri Seed Oil and Its Antibacterial Potential

Catalytic Fatty Acid Methyl Esters (FAMEs) Synthesis Using Lepidium aucheri Seed Oil and Its Antibacterial Potential

Life cycle assessment and biodegradability of biodiesel produced using different alcohols and heterogeneous catalysts

ABSTRACT The synthesis of fatty acid methyl (RME) and fatty acid butyl esters (RME) using heterogeneous catalysts (dolomite, eggshells, snail shells) is attractive as more and more legislations about global warming and energy security encourage to pay attention to renewable energy sources. In this study, the impact of six different RME and RBE production scenarios on the environment was investigated, also biodegradability research of RMEs and RBEs and mineral diesel were conducted. To assess life cycle, SimaPro9 software was used and impact to 11 environmental categories were evaluated. The environmental performance was determined based on their midpoint impacts, CML-IA baseline V3.06/EU25 method. Results of LCA showed that the production of RBE using eggshells and snail shells as heterogeneous catalysts had the most adverse impact on the global warming potential (2298.0 and 2266.1 kgCO2eq t−1 respectively). While the lowest impact to global warming potential was obtained for RME production using dolomite as a catalyst (1436.8 kgCO2eqt−1). The production of RME using dolomite had the lowest impact on almost all categories, while the synthesis of RBE using eggshells had the highest impact on the environment. However, conditions under which biodiesel is produced have a huge impact on life cycle assessment results. RMEs showed higher biodegradability compared with RBEs. HIGHLIGHTS LCA on six different biodiesel production scenarios was investigated. FAME production using dolomite has the lowest impact on the environment. Conditions under which biodiesel is produced have a huge impact on LCA results. Biodegradability of RMEs and RBEs was investigated. Biodegradability depends on the type of alcohol, not on the catalyst which was used.

Synthesis of ω-Hydroxy Fatty Acid Alkyl Esters by Macrocyclic Lactones Alcoholysis Catalyzed by Homoleptic and Heteroleptic Zinc Aryloxides.

A series of zinc aryloxides, [Zn4(sal-Me)8]⋅2.5(C7H8) (1), [Zn4(sal-Me)8]⋅CH2Cl2 (2), [Zn4(μ3-OR)2(sal-R)6] (3) (for R=Me (0.51), Et (0.49)), [Zn4(μ3-OMe)4(sal-Me)4(HOMe)4] (4), [Zn(sal-Me)2(py)2]⋅THF (5), {[Zn(sal-Me)2(tmbpy)] ⋅ 2(C6H5CH3)}n (6), [Zn2(sal-Me)2(THF)2Cl2] ⋅ 0.5(C6H5CH3) (7), and [Zn4(μ3-OMe)2(sal-Me)4Cl2] (8) (Hsal-Me=methyl salicylate, py=pyridine, tmbpy=4,4'-trimethylenedipyridine) were obtained that have different nuclearities and central core topologies and contain ligands of different basicity and coordination abilities.

Synthesis of Methyl Esters from Banda Nutmeg and Papua Nutmeg Oil Production Wastes Using the Ultrasonication Method

Methysters from oil production waste from Banda nutmeg (Myristicafragrans Houtt) and Papuan nutmeg (Myristica Argentea Ware) go through several process stages, namely isolation of trimyristin and synthesis of methyl ester. The process of isolating trimyristin from nutmeg essential oil production waste by maceration using chloroform solvent. The transesterification process with methanol uses a CaO catalyst and ultrasonication method for 20 minutes; the results are analyzed using GCMS. The results of isolating trimyristin from nutmeg oil waste for Papuan nutmeg yielded 55.6 g of trimyristin (22.24%), which was greater than Banda nutmeg which was 49.7 g of trimyristin (19.88%). Transesterification results for Banda nutmeg oil waste obtained 28.57% soakage with a composition of 5 known major methyl ester compounds, namely methyl laurate (3.22%), myristicin (13.48%), metal myristate (53.39%), methyl Palmitate (5.24%), and Methyl Oleate (9.33%). In Papuan nutmeg oil waste, a 3.93% soakage was obtained with a composition of 5 known methyl ester compounds, namely metal myristate (19.80%), methyl arachidate (18.04%), methyl linoleate (1.42%), methyl oleate ( 48.37%), and methyl stearate (3.18%). The sonication method can synthesize methyl esters from nutmeg oil waste and gives different results for the two types of nutmeg. The results of the trimyristin transesterification of Banda nutmeg seeds and Papuan nutmeg seeds using a CaO catalyst using the sonication method resulted in a methyl ester soak of Banda nutmeg waste 28.57% and Papuan nutmeg 3.93%.

Electrolysis Approach of Fatty Acid Methyl Ester Production Using Alkali Hydroxides and Their Alkoxides

The depletion of fossil fuels and environmental concerns have led to the search for alternative fuels (biodiesel) derived from renewable resources. Electrolysis is a promising method of fatty acid methyl ester (FAME) synthesis that can be maintained at room temperature. Nevertheless, the low reaction rates have been commonly accelerated using a combination of catalysts and electrolytes. This work proposed a novel electrolyte-free electrolysis approach for biodiesel synthesis from soybean oil using alkaline hydroxide (NaOH, KOH) and alkaline methoxide (NaOCH3, KOCH3)catalysts. Though all of them demonstrated high biodiesel yield, KOCH3 exhibitedthe highest efficiency. Based on response surface methodology, the highest FAME yield of 97.11% was achieved at optimal electrolysis voltage of 18.76V, water amount of 1.97 wt.%, KOCH3 amount of 3.17 wt.%, and methanol/oil of 21.33:1 molar, and reaction time of 60 min. The fuel properties of synthesized biodiesel agreed with international standards.The findings of this work suggest that electrolyte-free electrochemical using alkaline hydroxides and alkaline methoxides as catalysts could be a useful alternative to conventional transesterification method for producing biodiesel. Keywords: Alkaline catalysts, Biofuel, Box–Behnken Design, Electrochemical approach

Contribution of Malang quartzite-based silica in K2O/zeolite Y catalyst for methyl ester synthesis of off grade crude palm oil

Malang quartzite contains a highly silica content. The silica changes the structural composition of Zeolite Y. Currently, a heterogeneous catalyst is developed to optimize transesterification of Off Grade CPO (Crude Palm Oil). The aims of this study are: (1) synthesize K2O/Zeolite Y using silica from Malang quartzite, (2) synthesize methyl esters from Off Grade CPO using K2O/Zeolite Y catalyst, and (3) to evaluate quartzite based-silica contribution in Zeolite Y for the reaction activity via GC-MS analysis. The experimental stages were: the oil preparation, esterification of the prepared oil, preparation of K2O/zeolite Y catalyst, and the transesterification. This study applied variations of [KOH] in Zeolite Y (10, 20, and 30 % w/w) and the concentration of the transesterification catalyst (2, 3, and 4 % w/w). The K2O/Zeolite Y catalyst was successfully synthesized by impregnation method. Methyl esters of Off Grade CPO resulted the highest yield of 95.05 % with 4 wt% of 30-K2O/Zeolite Y (30 % KOH impregnation). The synthesized methyl esters have a density of 0.877 g/mL, a viscosity of 4.6 cSt, a refractive index of 1.445 and an acid number of 0.384 mg/g according to the standard (SNI 7182:2015). The main components of the methyl ester based on GC-MS results were methyl octanoate, methyl decanoate, methyl dodecanoate, methyl 9-octadecanoate, methyl octadecanoate and methyl tetracosanoate. Using quartzite-based silica, a co-activity of the reaction has occurred.

Solid Lipid Nanoparticles Based on Babassu Oil and Copaiba Oleoresin: A Promising Approach for Prostate Cancer Therapy.

Solid lipid nanoparticles (SLNs) represent promising nanostructures for drug delivery systems. This study successfully synthesized SLNs containing different proportions of babassu oil (BBS) and copaiba oleoresin (COPA) via the emulsification-ultrasonication method. Before SLN synthesis, the identification and quantification of methyl esters, such as lauric acid and β-caryophyllene, were performed via GC-MS analysis. These methyl esters were used as chemical markers and assisted in encapsulation efficiency experiments. A 22 factorial design with a center point was employed to assess the impact of stearic acid and Tween 80 on particle hydrodynamic diameter (HD) and polydispersity index (PDI). Additionally, the effects of temperature (8 ± 0.5 °C and 25 ± 1.0 °C) and time (0, 7, 15, 30, 40, and 60 days) on HD and PDI values were investigated. Zeta potential (ZP) measurements were utilized to evaluate nanoparticle stability, while transmission electron microscopy provided insights into the morphology and nanometric dimensions of the SLNs. The in vitro cytotoxic activity of the SLNs (10 µg/mL, 30 µg/mL, 40 µg/mL, and 80 µg/mL) was evaluated using the MTT assay with PC-3 and DU-145 prostate cancer cell lines. Results demonstrated that SLNs containing BBS and COPA in a 1:1 ratio exhibited a promising cytotoxic effect against prostate cancer cells, with a percentage of viable cells of 68.5% for PC-3 at a concentration of 30 µg/mL and 48% for DU-145 at a concentration of 80 µg/mL. These findings underscore the potential therapeutic applications of SLNs loaded with BBS and COPA for prostate cancer treatment.

Synthesis of microalgae-based methyl ester using calcium glyceroxide catalyst derived from duck eggshells and crude glycerol in the n-hexane co-solvent system

Abstract The synthesis of microalgae-based methyl ester has attracted the interest of researchers since microalgae have a high lipid content and can proliferate. Chlorella vulgaris, with its 63% lipid content on a dry basis, holds promise for methyl ester production. Heterogeneous catalysts, particularly calcium glyceroxide (Ca[O(OH)2C3H5]), play a crucial role in ester manufacturing due to their high catalytic activity. The synthesis of the calcium glyceroxide catalyst involves duck eggshells as a calcium source and crude glycerol. Optimal methyl ester production is achieved by employing n-hexane as a co-solvent for efficient microalgae oil dissolution. This research focuses on synthesizing and characterizing the calcium glyceroxide catalyst derived from duck eggshells and crude glycerol, emphasizing its application in manufacturing microalgae-based methyl esters with n-hexane as the co-solvent. Methyl ester synthesis variables include a 55°C reaction temperature, a 1.5% microalgae-derived catalyst, and a 9:1 methanol to microalgae ratio. FTIR functional group analysis identifies hydroxyl (O-H) groups from crude glycerol bound to calcium at 3345.71 cm−1, along with C-H group vibrations from crude glycerol bound to calcium at 2941.80 cm−1. SEM morphological analysis reveals aggregate formation on the calcium glyceroxide catalyst, indicating potential active sites. Utilizing the calcium glyceroxide catalyst for methyl ester synthesis yields a promising 62.42% yield. GC characterization demonstrates a methyl ester purity of 72.09%, with methyl palmitate as the predominant component at 30.927%. This study underscores the efficient use of the synthesized calcium glyceroxide catalyst for microalgae-based methyl ester production, showcasing its potential for sustainable biodiesel synthesis.

Synthesis of Methyl Ester from Microalgae Chlorella sp. TAD Using the In-Situ Transesterification Method

Synthesis of methyl ester from Chlorella sp. TAD microalgae was carried out using the in-situ transesterification method. This study aims to determine the methyl ester composition of Chlorella sp. TAD microalgae using the in-situ transesterification method. The in-situ transesterification method is a modified method that allows extraction and transesterification into methyl ester products in one process simultaneously. The in-situ transesterification process lasted 8 hours, followed by a distillation process to remove the n-hexane content and an oven for 2 hours to evaporate the remaining water. The results of the analysis using GC-MS to determine the chemical content of the methyl ester compound from Chlorella sp. TAD, showed the methyl ester composition of 7,10-hexadecanoic methyl ester, 8,11,14-docosatrienoic methyl ester, 9-hexadecanoic methyl ester, hexadecanoic methyl ester, heptadecanoic methyl ester, 10-octadecenoic methyl ester, octadecenoic methyl ester, 9,12-octadecadienoic methyl ester, 10-octadecenoic methyl ester, 2-hexyl cyclopropaneoctanoic methyl ester, eicosanoic methyl ester, 10-heptadecen-8-ynoic acid methyl ester, nonahexacontanoic methyl ester, and tetracosanoic methyl ester.

Magnetic induction heating-assisted synthesis of biodiesel using an alumina/iron oxide nanocatalyst

While generating biodiesel from vegetable oils presents various advantages over fossil fuels, ongoing actions aim to improve the efficiency of this production process. Emphasis is placed on optimizing experimental conditions, including the catalyst selection, reaction media and the energy source for heating and mixing, thereby revealing existing research gaps in biodiesel production. In this sense, we have designed a magnetic nanocatalyst based on iron oxide nanoparticles (IONPs) of 18 nm in diameter incorporated within an alumina matrix of around 500 nm infused with potassium hydroxide that provides the catalyst's mesoporosity and basicity. Magnetization analyses confirmed the superparamagnetic behaviour of the nanocatalyst at room temperature and a saturation magnetisation high enough to ease magnetic recovery for reuse. Additionally, magnetic nanoparticles can serve as nanoheaters when subjected to an alternating magnetic field. The heating efficiency of the isolated IONPs was assessed under various frequency and field conditions, yielding specific absorption rate values of up to 80 W/g. Such heating capacity has allowed the synthesis of fatty acid methyl ester (FAMEs), which constitute the biodiesel at 65 °C under optimal field conditions (100 kHz and 48 kA/m) and ideal reaction parameters: 5 % catalyst, methanol/oil ratio 12:1 and 6 h of reaction, with a conversion of up to 98.6 % determined through NMR characterization of the FAMEs and a 95.6 % yield. FAMEs presence was confirmed by optimizing a swift and efficient FTIR method and their purity by TLC. Overall, the designed nanocatalyst presented for FAME synthesis, which incorporates magnetic separability and effective heating capabilities, holds great promise for cost reduction and process efficiency.

Optimization of methyl ester synthesis using gas/liquid phase pulsed discharge plasma in a novel oscillatory slug flow reactor

In the present research, an innovative oscillatory slug flow reactor (OSFR) under the treatment of gas–liquid phase pulsed discharge plasma was developed for biodiesel production. The main goal was continuous production of high quality biodiesel at low temperature and pressure. Experimental tests were carried out under the influence of four main operating parameters including applied voltage, molar ratio, reactant flow rate, and catalyst concentration. The response surface method was employed to optimize experimental tests. The results showed that the proposed technology provided 94% production efficiency under the optimal conditions of voltage 19.4 kV, molar ratio 6.4, flow rate 2.7 ml/s, and catalyst 0.9 wt. %. According to the statistical analysis, increasing the applied voltage and reducing the flow rate have a strong effect on the Fatty Acid Methyl Ester yield, while the concentration of potassium hydroxide and methanol have less effect on the overall efficiency. In addition, the characteristics of the produced biodiesel were in accordance with ASTM D6751 standards. Surprisingly, the optimal energy consumption in this system was 95 kJ/l, which is more economically viable. In general, this study showed that the combined system of gas/liquid phase plasma in the OSFR reactor has a high synergistic potential for the transesterification reaction.

Optimization, characterization, and GC-MS analysis of CSOME produced using alkali catalyzed transesterification

Biodiesel (methyl ester) was synthesized from cottonseed oil (CSO) with methanol in the presence of an alkali catalyst (KOH) through the transesterification method. Response surface methodology (RSM) optimized the methyl ester synthesis process. The experimental design matrix was arranged using the Box-Behnken Design (BBD) of RSM. The optimization of methyl ester was achieved by varying variables such as the methanol to CSO ratio, the concentration of the catalyst, and the reaction duration. A contour plot and a surface plot were generated to illustrate the impact of these variables on methyl ester synthesis. The biodiesel yield was modeled as a quadratic equation through RSM analysis, with a coefficient of determination (R2) and adjusted R2 of 0.97 and 0.968, respectively. The optimized CSOME yield (95.04%) was numerically gained at a 1:6 methanol to CSO ratio, a reaction duration of 52.2 min, and a 0.985 wt% catalyst concentration. Based on these parameters, a 94.80% CSOME yield was experimentally obtained. This shows that response surface methodology (RSM) is sufficient for optimizing methyl ester yield. The produced methyl ester was characterized to determine its physicochemical properties. Gas chromatography-mass spectrometry (GC-MS) analysis was used to identify the specific type and proportion of fatty acid esters present in the CSOME. The main types of fatty acids found in CSOME were methyl 9-cis 11-trans-octadecadienoate (C18:2), hexadecanoic acid methyl ester (C16:0), 11, 14-octadecadienoic acid methyl ester (C18:2), methyl 8, 9-octadecadienoate methyl ester (C18:2), and myristic acid methyl ester (C14:0).

Heterogeneous Base Catalyst from Hybrid Banana-and-Plantain Peels in papaya Seed Oil (Carica papaya) Methyl-Ester Synthesis

Heterogeneous Base Catalyst from Hybrid Banana-and-Plantain Peels in papaya Seed Oil (Carica papaya) Methyl-Ester Synthesis

Synthesis of Biodiesel from Refined Waste Cooking Oil with Active Natural Zeolite

This research evaluates refining waste cooking oil with active natural zeolite, utilizes it for biodiesel synthesis, and characterizes the synthesized methyl ester. This experimental laboratory research was carried out: (1) activation of natural zeolite, (2) refining waste cooking oil with active natural zeolite, (3) determination of free fatty acid (FFA) content of the oil, (4) transesterification with KOH catalyst, (5) characterization of the synthesized methyl esters according to the SNI 7182:2015, and (6) identification of the methyl ester component by GC-MS. The results showed that the FFA content of the refined waste cooking oil using active natural zeolite with concentrations of 10%, 20%, and 30% per mass of oil were 2.97, 2.0, and 1.56%, respectively. The yield of methyl ester transesterified with various concentrations of KOH (0.8, 1.0, and 2% per mass of oil), respectively, were 80.13, 85.34, and 74.98%. The synthesized methyl ester resulted in the characteristics: 0.867 g/mL of density; 5.72 cSt of viscosity; 1.449 of refractive index; 1.46 g KOH/g of acid number; and 0.023% of water content. Identification of GC-MS obtained the synthesized methyl esters, which include: 46.10% of methyl hexadecanoic, 41.68% of methyl 9-octadecanoic, 6.42% of methyl octadecanoic, and 5.80% of methyl eicosanoic.

Catalytic Performance Investigation of Alkali and Bifunctional Catalysts Derived from Lignocellulosic Biomasses for Biodiesel Synthesis from Waste Frying Oil.

In this study, alkali and bifunctional catalysts were synthesized for waste frying oil methyl ester (WFOME) synthesis. Coffee husk (CH) and CH blended with Eragrostis tef straw (TS) (CH-TS) lignocellulosic biomasses (LBs) were utilized during the catalysts' synthesis. The alkali catalysts were CH and CH-TS ashes, both modified by KNO3 impregnation. They are designated as C-45 and C-Mix, respectively. Zirconia (ZrO2) promoted CH ash catalysts via precipitation followed by impregnation (Bic-PP) and in situ precipitation-impregnation (Bic-Dm) were the bifunctional ones. CH and CH-TS chars were the supporting frameworks during the catalysts' composite materials (CCMs) preparation. The combustion performance of LBs and CCMs was evaluated and associated with the catalysts' physicochemical properties. Using XRD, SEM, FTIR, alkalinity, TOF, and BET surface area analysis, catalysts were characterized. The combustion performance of the LBs was in the order of TS > CH-TS > CH. Among CCMs, the highest combustion performance was for CCM-Mix (KNO3/(CH-TS char)) and the lowest was for CCM-45 (KNO3/ CH char). The C-Mix catalyst was a light green powder due to the reaction between inorganic components, whereas C-45 was dark gray due to the presence of unburned char. The CCMs for bifunctional catalysts had moderate combustion performance and yielded light gray powdered catalysts containing tetragonal ZrO2. The optimum WFOME yields were 98.08, 97, 92.69, and 93.05 wt % for C-Mix, C-45, Bic-Dm, and Bic-PP assisted WFO transesterification, respectively. The results were obtained at a reaction temperature of 65 °C, time of 1 h, and methanol to WFO molar ratio of 15:1 using catalyst amounts of 5 and 7 wt % for the alkali and bifunctional catalysts, respectively. The greatest moisture resistance was offered by the C-Mix catalyst. The best reusability was for the C-45 catalyst. Catalysts' deactivation modes include active site leaching and poisoning.

Synthesis and biological evaluation of natural Lachnophyllum methyl ester, Lachnophyllum lactone and their synthetic analogs.

(2Z)-Lachnophyllum methyl ester and (4Z)-Lachnophyllum lactone were recently identified as major components in essential oils and extracts of Conyza bonariensis from Togo. Extended biological evaluation of these acetylenic compounds was however hampered by the reduced amounts isolated. A synthetic route was designed providing access to larger quantities of these two natural products as well as to original non-natural analogs with the prospect of exploring for the first time the structure-activity relationships in this series. Using LC/MS analysis, synthetic samples allowed confirming the presence of the two previously isolated natural products in plant extracts obtained by the accelerated solvent extraction technique. The nematocidal activity of the synthesized compounds confirmed the potency of the natural products, which remain the most active among all analogs tested. The synthesized compounds were also assessed against Leishmania infantum axenic amastigotes and the Mycobacterium tuberculosis H37Rv pathogenic strain. (2Z)-Lachnophyllum methyl ester, (4Z)-Lachnophyllum lactone and lactone analogs exhibited the strongest antileishmanial potency. As expected, a longer alkyl chain was necessary to observe significant antimycobacterial activity. The lactone analog bearing a C10 lipophilic appendage displayed the highest antimycobacterial potency. The notable activities of lactones, naturally occurring or analogs, either nematicidal, antileishmanial or antimycobacterial, were compared to their cytotoxicity for mammalian cells and revealed moderate selectivity index values. In this regard, the innocuous (2Z)-Lachnophyllum methyl ester and its analogs open up more promising perspectives for the discovery of bioactive agents to protect both agricultural crops and human health.

Synthesis of alkyl-branched fatty acids by isomerization on micro-mesoporous ferrierite-based zeolitic materials

The synthesis of alkyl-branched fatty acid methyl esters from fatty acids is of great interest to synthesize high value-added products. The isomerization reaction catalyzed by microporous zeolites is promising due to its high yields, but rapid deactivation is its main drawback. In this work, a micromesoporous ferrierite synthesized by a well-controlled alkaline recrystallization process, was evaluated as a catalyst in the isomerization of methyl oleate. Recrystallized materials present improved accessibility of acid sites at the mouth of 10-MR pores due to the increase of the mesopore surface. Methyl oleate isomerization has been implemented in batch conditions and in a continuous flow process with experiments lasting more than 3 days. Stable yield of branched isomers higher than 50% was reached at 285 °C and 3.5 h-1 WHSV. The catalytic results, combined with a detailed analysis of fresh and spent catalysts, has provided information on the phenomena involved, in particular deactivation.

Methyl oleate for plant protection products formulations: Enzymatic synthesis, reaction kinetics and application testing

This study presents a solvent-free enzymatic approach for the synthesis of fatty acid methyl esters (FAMEs), such as methyl oleate, for their application as adjuvant in plant protection products (PPP) formulations. The direct esterification between free fatty acid and methanol was optimized to achieve 98% acid conversion. The kinetics of this conversion was accurately described by a simple second order mechanism and non-linear regression was applied to calculate the rate constants of the forward and backward reactions based on full progress curves data. The rate constant of the forward reaction (synthesis) was one order of magnitude higher than the backward reaction (hydrolysis) and favored formation of the target methyl ester product, rendering the removal of water unnecessary. Enzymatically synthesized methyl oleate was benchmarked against the chemically synthesized compound, showing matching results in terms of stability, spreadability and emulsifying capacity in plant care formulations. The enzymatic synthesis of FAMEs under solvent free conditions allows to achieve a safer and more sustainable character for carrier solvents in PPP formulations.

Production of 2,5-Furandicarboxylic Acid Methyl Esters from Pectin-Based Aldaric Acid: from Laboratory to Bench Scale.

2,5-Furandicarboxylic acid (FDCA) is one of the most attractive emerging renewable monomers, which has gained interest especially in polyester applications, such as the production of polyethylene furanoate (PEF). Recently, the attention has shifted towards FDCA esters due to their better solubility as well as the easier purification and polymerisation compared to FDCA. In our previous work, we reported the synthesis of FDCA butyl esters by dehydration of aldaric acids as stable intermediates. Here, we present the synthesis of FDCA methyl esters in high yields from pectin-based galactaric acid using a solid acid catalyst. The process enables high substrate concentrations (up to 20 wt %) giving up to 50 mol % FDCA methyl esters with total furancarboxylates yields of up to 90 mol %. The synthesis was successfully scaled up from gram-scale to kilogram-scale in batch reactors showing the feasibility of the process. The stability of the catalyst was tested in re-use experiments. Purification of the crude product by vacuum distillation and precipitation gave furan-2,5-dimethylcarboxylate with a 98 % purity.

Optimization Study of Methyl Ester (Biodiesel) Synthesis from Chicken Tallow Using Polyoxomolybdate Catalyst

Optimization Study of Methyl Ester (Biodiesel) Synthesis from Chicken Tallow Using Polyoxomolybdate Catalyst