Characterisation and performance of three promising heterogeneous catalysts in transesterification of palm oil

2012 ◽  
Vol 66 (3) ◽  
Author(s):  
Wan Isahak ◽  
Manal Ismail ◽  
Jamaliah Jahim ◽  
Jumat Salimon ◽  
Mohd Yarmo

AbstractIn this work, the performance of three heterogeneous catalysts, namely potassium hydroxide/γ-alumina, bulk calcium oxide, and nano-calcium oxide, in comparison with the homogeneous potassium hydroxide was studied in the transesterification of palm oil to produce methyl esters and glycerol. The physical and chemical properties of the heterogeneous catalysts were thoroughly characterised and determined using a number of analytical methods to assess their catalytic activities prior to transesterification. The reaction products were analysed using liquid chromatography and their properties were quantified based on the American Society of Testing and Materials and United State Pharmacopoeia standard methods. At the 65°C reaction temperature, the oil-to-methanol mole ratio of 1: 15, 2.5 h of the reaction time, and catalyst (φ r = 1: 40), potassium hydroxide, potassium hydroxide/γ-alumina, nano-calcium oxide, and bulk calcium oxide gave methyl ester yields of 97 %, 96 %, 94 %, and 90 %, respectively. The impregnation of γ-alumina with potassium hydroxide displayed a catalytic performance comparable with the performance of potassium hydroxide where the former could be physically separated via filtration resulting in a relatively greater purity of products. Other advantages included the longer reusability of the catalyst and more active sites with lower by-product formation.

Catalysts ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1085
Author(s):  
Shafaq Nisar ◽  
Muhammad Asif Hanif ◽  
Umer Rashid ◽  
Asma Hanif ◽  
Muhammad Nadeem Akhtar ◽  
...  

The effective transesterification process to produce fatty acid methyl esters (FAME) requires the use of low-cost, less corrosive, environmentally friendly and effective catalysts. Currently, worldwide biodiesel production revolves around the use of alkaline and acidic catalysts employed in heterogeneous and homogeneous phases. Homogeneous catalysts (soluble catalysts) for FAME production have been widespread for a while, but solid catalysts (heterogeneous catalysts) are a newer development for FAME production. The rate of reaction is much increased when homogeneous basic catalysts are used, but the main drawback is the cost of the process which arises due to the separation of catalysts from the reaction media after product formation. A promising field for catalytic biodiesel production is the use of heteropoly acids (HPAs) and polyoxometalate compounds. The flexibility of their structures and super acidic properties can be enhanced by incorporation of polyoxometalate anions into the complex proton acids. This pseudo liquid phase makes it possible for nearly all mobile protons to take part in the catalysis process. Carbonaceous materials which are obtained after sulfonation show promising catalytic activity towards the transesterification process. Another promising heterogeneous acid catalyst used for FAME production is vanadium phosphate. Furthermore, biocatalysts are receiving attention for large-scale FAME production in which lipase is the most common one used successfully This review critically describes the most important homogeneous and heterogeneous catalysts used in the current FAME production, with future directions for their use.


Synlett ◽  
2019 ◽  
Vol 30 (06) ◽  
pp. 699-702 ◽  
Author(s):  
Yu Hu ◽  
Nan Yao ◽  
Jin Tan ◽  
Yang Liu

A range of multifunctional magnetic metal–organic framework nanomaterials consisting of various mass ratios of the metal–organic framework MIL-53(Fe) and magnetic SiO2@NiFe2O4 nanoparticles were designed, prepared, characterized, and evaluated as heterogeneous catalysts for the Knoevenagel condensation. The as-fabricated nanomaterials, especially the nanocatalyst MIL-53(Fe)@SiO2@NiFe2O4(1.0), showed good catalytic performance in the Knoevenagel condensation at room temperature as a result of synergistic interaction between the Lewis acid iron sites of MIL-53(Fe) and the active sites of the magnetic SiO2@NiFe2O4 nanoparticles. In addition, the heterogeneous catalyst was readily recovered and a recycling test showed that it could be reused for five times without significant loss of its catalytic activity, making it economical and environmentally friendly.


Energies ◽  
2021 ◽  
Vol 14 (17) ◽  
pp. 5506
Author(s):  
Daniel Carreira Batalha ◽  
Márcio José da Silva

Nowadays, the synthesis of biofuels from renewable raw materials is very popular. Among the various challenges involved in improving these processes, environmentally benign catalysts compatible with an inexpensive feedstock have become more important. Herein, we report the recent advances achieved in the development of Niobium-containing heterogeneous catalysts as well as their use in routes to produce biodiesel. The efficiency of different Niobium catalysts in esterification and transesterification reactions of lipids and oleaginous raw materials was evaluated, considering the effect of main reaction parameters such as temperature, time, catalyst load, and oil:alcohol molar ratio on the biodiesel yield. The catalytic performance of Niobium compounds was discussed considering the characterization data obtained by different techniques, including NH3-TPD, BET, and Pyr-FT-IR analysis. The high catalytic activity is attributed to its inherent properties, such as the active sites distribution over a high specific surface area, strength of acidity, nature, amount of acidic sites, and inherent mesoporosity. On top of this, recycling experiments have proven that most Niobium catalysts are stable and can be repeatedly used with consistent catalytic activity.


Catalysts ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1005
Author(s):  
Daniel Ruano ◽  
Beatriz M. Pabón ◽  
Càtia Azenha ◽  
Cecilia Mateos-Pedrero ◽  
Adélio Mendes ◽  
...  

In this work, the electronic properties of the metal sites in cubic and monoclinic ZrO2 supported Pd and PdCu catalysts have been investigated using CO as probe molecule in in-situ IR studies, and the surface composition of the outermost layers has been studied by APXPS (Ambient Pressure X-ray Photoemission Spectroscopy). The reaction products were followed by mass spectrometry, making it possible to relate the chemical properties of the catalysts under reaction conditions with their selectivity. Combining these techniques, it has been shown that the structure of the support (monoclinic or cubic ZrO2) affects the metal dispersion, mobility, and reorganization of metal sites under methanol steam reforming (MSR) conditions, influencing the oxidation state of surface metal species, with important consequences in the catalytic activity. Correlating the mass spectra of the reaction products with these spectroscopic studies, it was possible to conclude that electropositive metal species play an imperative role for high CO2 and H2 selectivity in the MSR reaction (less CO formation).


2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Anil Kumar ◽  
Henry K. Kiriamiti

Transesterification kinetics of Croton megalocarpus oil to produce fatty acid methyl esters (FAME) was studied using homogeneous NaOH and heterogeneous alkaline earth Nano MgO, MgO, Nano CaO, CaO, Reoxidized CaO, SrO, and BaO catalysts. Characteristic surface, bulk, and chemical properties of the heterogeneous catalysts were obtained which included surface area, pore properties, scanning electron micrography, X-ray diffraction, basic strength, and basicity. The catalyst porosity varied as Nano MgO > Nano CaO > MgO > CaO > CaO-RO > SrO > BaO and basicity as BaO > SrO > Nano CaO > CaO RO > CaO > Nano MgO > MgO. Catalysts NaOH, BaO, SrO, and Nano CaO gave a good FAME yield (>50%), and reaction order and rate constant have been reported for these catalysts, for both conventional heating and microwave irradiation. The overall reaction for NaOH was of 1st order for microwave irradiation with respect to triglyceride and of 2nd order with respect to triglyceride under conventional heating. For the heterogeneous catalysts, the overall reaction was of 3rd order, 2nd order with respect to triglyceride and 1st order with respect to methanol for both heating methods. Reaction rate constants for microwave irradiation were higher than those for conventional heating due to faster reaction rates under such heating. BaO was the most active heterogeneous catalyst, followed by SrO and Nano CaO, which was in accordance with their basicity.


2020 ◽  
Vol 8 ◽  
Author(s):  
Shuhua Hao ◽  
Xinpei Zhao ◽  
Qiyang Cheng ◽  
Yupeng Xing ◽  
Wenxuan Ma ◽  
...  

The successful preparation and application of graphene shows that it is feasible for the materials with a thickness of a single atom or few atomic layers to exist stably in nature. These materials can exhibit unusual physical and chemical properties due to their special dimension effects. At present, researchers have made great achievements in the preparation, characterization, modification, and theoretical research of 2D materials. Because the structure of 2D materials is often similar, it has a certain degree of qualitative versatility. Besides, 2D materials often carry good catalytic performance on account of their more active sites and adjustable harmonic electronic structure. In this review, taking 2D materials as examples [graphene, boron nitride (h-BN), transition metal sulfide and so on], we review the crystal structure and preparation methods of these materials in recent years, focus on their photocatalyst properties (carbon dioxide reduction and hydrogen production), and discuss their applications and development prospects in the future.


Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 724
Author(s):  
Zuchra Helwani ◽  
Muliadi Ramli ◽  
Edy Saputra ◽  
Yogi Lesmana Putra ◽  
Desly Fadila Simbolon ◽  
...  

This research was designed to synthesize a composite catalyst of palm oil fly ash-impregnated calcium oxide prepared from eggshell waste. Several preparation conditions, such as temperature and time applied to calcination and dehydration processes, were investigated. As a result, the optimum temperature and the length of time of calcination were 900 °C and 3 h, respectively. Meanwhile, the dehydration process was performed optimally at 600 °C for 3 h. The X-ray diffraction (XRD) results indicate that the obtained catalyst mostly contained calcium oxide compounds (CaO and Ca(OH)2) and minor impurities of silica oxides (SiO2 and Ca2SiO4), with a catalyst-specific surface area of 30.24 m2/g. Regarding its catalytic performance, the composite catalyst proved successful for prospective application the in transesterification of palm oil off-grade, resulting in methyl palmitate and methyl oleate, which are two biodiesel compounds.


2021 ◽  
Vol 18 ◽  
Author(s):  
Vivek Srivastava

: The catalytic display of supported heterogeneous catalysts is essentially reliant on their constitutive elements including active species and supports. Accordingly, the scheme and development of active catalysts with synergistically enhanced outcomes between active sites and supports are of high importance. A simple NaBH4 reduction method was used to synthesize cylindrical amine-functionalized silica nanotubes supported Ru catalyst (ASNT@Ru catalyst) including amine functionality. The physicochemical properties of the material were analyzed by various analytical methods such as SEM-TEM analysis, N2 physisorption, ICP-OES, XPS, etc, and all the data were found in good agreement with each other. Amine-free SNT support using the calcination process was also synthesized to examine the effect of amine in ASNT support on the uniform Ru dispersion. Taking the advantages of the fundamental physical and chemical properties of ASNT support and well-distributed Ru NPs, the ASNT@Ru catalyst was utilized for CO2 hydrogenation reaction and gave excellent catalytic activity/ stability in terms of a good quantity of the formic. 5 times catalysts recycling were recorded, and formic acid was obtained in good quantity.


2018 ◽  
Vol 6 (3) ◽  
pp. 705
Author(s):  
Tirto Prakoso ◽  
Indra B Kurniawan ◽  
R Heru Nugroho

Methyl esters are one of alkyl esters compound that used as alternative diesel fuel became popular. Methyl esters have similarities on physical and chemical properties with the diesel fuel produced from fossil oil; however it has less combustion and environmental emissions. As fossil oil become rare to be exploited, and the rapid environmental issues, the efforts to develop methyl esters as alternative diesel fuel become a prospective one. One method to produce methyl esters from free fatty acids of crude palm oil (CPO) is the two step esterification-transesterification reaction, each step produce the same final product, however differs in the side product. Esterification produce water and transesterfication produce glycerin. The reaction uses alcohol as main reactant beside the free fatty acids, it can be conducted in batch or continuous production. In this research, the investigation is only emphasized in the first step that is the esterification step to produce methyl esters from free fatty acids contained in crude palm oil. Methanol and sulfuric acid are used as reactant and catalyst respectively. Methyl esters produced by esterification is affected by reaction temperature, amounts of catalyst, and methanol volume. The increase in temperature improved esterification conversion from 19% in 50C to 98% in 60C. While the usage of the highest amount of catalyst, 5 ml/1-CPO, led to produced the highest conversion relative to the conversion from 1 and 3 ml/1-CPO catalyst. Furthermore, 10% amount of methanol per volume CPO produced higher yield than 8%.Keywords : Biodiesel,  CPO Free Fatty Acid Esterification, Methyl Ester ConversionAbstrak Metil ester merupakan suatu senyawa alkil ester yang dapat digunakan sebagai bahan bakar alternatif. Metil ester memiliki sifat fisik dan kimia yang hampir sam a dengan minyak diesel yang dihasilkan dari minyak bumi tetapi emisi pembakaran dari penggunaan ester metal lebih rendah dari pada emisi hasil penggunaan minyak solar. Seiring dengan semakin langkanya sumber minyak bumi dan semakin gencarnya isu lingkungan hidup, pengembangan ester metil sebagai bahan bakar pengganti minyak solar semakin prospektif. Pembuatan ester metil dari asam lemak bebas minyak sawit mentah (crude palm oil) dapat dilakukan dengan beberapa cara antara lain dengan reaksi esterifikasi dan transesterifikasi menggunakan alkohol. Reaksi-reaksi ini dapat dilaksanakan secara batch maupun kontinu. Pada penelitian yang telah dilakukan, pembuatan ester metil dari asam lemak bebas minyak sawit mentah dilakukan dengan reaksi esterifikasi secara batch, dengan reaktan berupa minyak sawit mentah dan metanol. Katalis yang digunakan adalah H2SO4. Konversi ester metil yang dihasilkan dipengaruhi oleh temperatur reaksi, konsentrasi katalis dan konsentrasi metanol. Kenaikan temperatur reaksi akan meningkatkan konversi dari 19% pada 50oC menjadi 98% pada 60oC. Dengan menggunakan konsentrasi katalis tertinggi 5ml/l CPO memicu konversi tertinggi relatif dibandingkan nilai konversi dari 1 dan 3 ml/l CPO. 10% metanol menghasilkan perolehan tinggi dibanding 8%.Kata Kunci: Biodiesel, EsterifikasiAsam Lemak Bebas CPO, Konversi Ester Metil


2018 ◽  
Vol 5 (5) ◽  
pp. 653-672 ◽  
Author(s):  
Leilei Zhang ◽  
Yujing Ren ◽  
Wengang Liu ◽  
Aiqin Wang ◽  
Tao Zhang

Abstract The green synthesis of fine chemicals calls for a new generation of efficient and robust catalysts. Single-atom catalysts (SACs), in which all metal species are atomically dispersed on a solid support, and which often consist of well-defined mononuclear active sites, are expected to bridge homogeneous and heterogeneous catalysts for liquid-phase organic transformations. This review summarizes major advances in the SAC-catalysed green synthesis of fine chemicals in the past several years, with a focus on the catalytic activity, selectivity and reusability of SACs in various organic reactions. The relationship between catalytic performance and the active site structure is discussed in terms of the valence state, coordination environment and anchoring chemistry of single atoms to the support, in an effort to guide the rational design of SACs in this special area, which has traditionally been dominated by homogeneous catalysis. Finally, the challenges remaining in this research area are discussed and possible future research directions are proposed.


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