scholarly journals Green Heterogeneous Base Catalyst from Ripe-Unripe Plantain Peels for the Transesterification of Waste Cooking Oil

2021 ◽  
Author(s):  
Olayomi Abiodun Falowo ◽  
Babatunde Oladipo ◽  
Abiola Ezekiel Taiwo ◽  
Tomiwa Ayomiposi Olaiya ◽  
Oluwaseun Oyekola ◽  
...  
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Waste Cooking Oil ◽  
Molar Ratio ◽  
Base Catalyst ◽  
Catalyst Amount ◽  
X Ray ◽  
Cooking Oil ◽  
Heterogeneous Base Catalyst ◽  
Heterogeneous Base

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.

Comparison of Biodiesel Production between Homogeneous and Heterogeneous Base Catalysts

2016 ◽  
Vol 833 ◽  
pp. 71-77 ◽  
Author(s):  
Yie Hua Tan ◽  
Mohammad Omar Abdullah ◽  
Cirilo Nolasco Hipolito
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Biodiesel Production ◽  
Molar Ratio ◽  
Optimum Operating ◽  
Homogeneous Catalyst ◽  
Base Catalyst ◽  
Optimum Operating Condition ◽  
Heterogeneous Base Catalyst ◽  
Heterogeneous Base

Homogeneous base catalyst has wide acceptability in biodiesel production because of their fast reaction rates. However, postproduction costs incurred from aqueous quenching, wastewater and loss of catalysts led to the search for alternatives. Heterogeneous base catalyst is developed to cater these problems. The advantages of heterogeneous catalyst are their high basicity and non-toxicity. This work compared the production of biodiesel using two different kind of catalysts that is homogeneous catalyst (sodium hydroxide, NaOH and potassium hydroxide, KOH) and heterogeneous catalysts (calcium, oxide, CaO catalyst derived from chicken and ostrich eggshells). Transesterification of waste cooking oil (WCO) and methanol in the presence of heterogeneous base catalyst was conducted at an optimal reaction condition (calcination temperature for catalyst: 1000 °C; catalyst loading amount: 1.5 wt%; methanol/oil molar ratio: 10:1; reaction temperature: 65 °C; reaction time: 2 hours) with 97% biodiesel yield was obtained. While, the homogeneous base catalyst gave higher biodiesel yield of 98% at optimum operating condition (catalyst concentration: 0.75 wt%; methanol/oil molar ratio: 6:1; reaction temperature: 65 °C; reaction time: 1 hours). The slight difference in the biodiesel yield was due to the stronger basic strength in the homogeneous catalyst and were not statistically not different (p=0.05). However, despite these advances, the ultimate aim of producing biodiesel at affordable low cost and minimal-environmental-impact is yet to be realized.

Effects of Microwave and Additional Co–Solvents on Two–Stage Waste Cooking Oil to Biodiesel Conversion

2012 ◽  
Vol 209-211 ◽  
pp. 1136-1141
Author(s):  
Ming Chien Hsiao ◽  
Yung Hung Chang ◽  
Li Wen Chang
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Waste Cooking Oil ◽  
Molar Ratio ◽  
Phase System ◽  
Reaction Conditions ◽  
Two Stage ◽  
Second Stage ◽  
Cooking Oil ◽  
Standard Value

This paper introduced a better solution to accelerating the production of biodiesel from waste cooking oil by using suitable acidic and alkaline catalysts in a two-stage catalytic reaction. Next, a co-solvent named tetrahydrofuran (THF), which significantly increased mixing level of the reactants in the mixture of vegetable oil and methanol, was added to form a single phase system. The whole system was then put into a microwave oven to support heat for the transesterification of biodiesel to shorten the reaction time. Reaction conditions of the first stage were methanol to oil molar ratio of 9:1, catalyst amount 1wt%, reaction temperature 60 oC and reaction time 7.5 minutes. In the second stage, for the transesterification, reaction conditions were methanol to oil molar ratio 12:1, catalyst loadings 1 wt%, reaction temperature 60 oC and reaction time 1.5 minutes. Finally, the conversion rate of biodiesel after the nine-minute reaction time was 97.38% which was higher than the EU EN14214 standard value of 96.5%.

Biodiesel Production through Direct Transesterification of Waste Cooking Oil with Alcohol via Ultrasonic Wave

2013 ◽  
Vol 389 ◽  
pp. 12-16
Author(s):  
Yong Feng Kang ◽  
Hua Jin Shi ◽  
Lin Ge Yang ◽  
Jun Xia Kang ◽  
Zi Qi Zhao
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Waste Cooking Oil ◽  
Biodiesel Production ◽  
Molar Ratio ◽  
Ultrasonic Power ◽  
Cooking Oil ◽  
Biodiesel Synthesis ◽  
Optimum Reaction ◽  
Ester Exchange Reaction

Biodiesel is prepared from waste cooking oil and methanol. The ester exchange reaction is conducted under ultrasonic conditions with alkali as the catalysts. Five factors influencing on the transesterification reaction of biodiesel production are discussed in this study, including the reaction time, reaction temperature, catalyst amount, methanol to oil molar ratio, ultrasonic power. A series of laboratory experiments were carried out to test the conversion of biodiesel under various conditions. The process of biodiesel production was optimized by application of orthogonal test obtain the optimum conditions for biodiesel synthesis. The results showed that the optimum reaction conditions were:molar ratio of oil to methanol 8:1,catalysts 1.2g KOH/100g oil,reaction temperature 70°C, reaction time 50 min,Ultrasonic power 400W. The conversion may up to 96.48%.

Application of Calcium Methoxide as Solid Base Catalyst for Biodiesel Production from Waste Cooking Oil

2016 ◽  
Vol 723 ◽  
pp. 594-598 ◽  
Author(s):  
Nichaonn Chumuang ◽  
Vittaya Punsuvon
Keyword(s):  
Reaction Temperature ◽  
Catalyst Concentration ◽  
Waste Cooking Oil ◽  
Transesterification Reaction ◽  
Biodiesel Production ◽  
Molar Ratio ◽  
Solid Base ◽  
Base Catalyst ◽  
Solid Base Catalyst ◽  
Cooking Oil

In this study, the biodiesel production of waste cooking oil using calcium methoxide as solid base catalyst was investigated. The calcium methoxide catalyst was synthesized from calcined quick lime reacted with methanol. The XRD result showed that the catalyst was successfully synthesized with sufficient purity. The strength of catalyst was examined on the transesterification reaction of waste cooking oil and methanol. Parameters affecting on transesterification such as the catalyst concentration, methanol-to-oil-molar ratio, reaction time and reaction temperature were investigated. The results showed that the percentage of fatty acid methyl ester conversion of 99.06%. The optimum conditions were achieved within 3 h using 3wt% catalyst concentration, 12:1 methanol-to-oil molar ratio and 65°C reaction temperature. In addition, the kinetic study of transesterification reaction was carried out at the temperature from 30°C to 65°C. The pseudo-first order was good agreement with the experiment results. The reaction rate constant (k) and activated energy (Ea) were determined as 0.023 min-1 and 55.77 kJ/mol, respectively.

Transesterification of Waste Cooking Oil to Produce Biodiesel Using Acid and Alkaline Catalyst

2012 ◽  
Vol 518-523 ◽  
pp. 3566-3572 ◽  
Author(s):  
Jin Li ◽  
Hou Bo Zhou ◽  
Yang Cao
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Maximum Yield ◽  
Energy Resource ◽  
Clean Energy ◽  
Waste Cooking Oil ◽  
Fatty Acid Esters ◽  
Molar Ratio ◽  
Alkaline Catalyst ◽  
Cooking Oil

Fossil oil as a nonrenewable energy resource, with the development of global economy, the need for energy increases continuously. Biodiesel is a renewable and clean energy, which is made by vegetable oil or animal fat and methyl alcohol to produce fatty acid esters. This research shows that waste cooking oil can be used for biodiesel by the means of esterification and transesterification, at the same time waste cooking oil can be reused. Through orthogonal design, the optimum conditions are that at first ,using sulfuric acid 5wt% of waste cooking oil as catalyst, the molar ratio of methanol and oil is 30:1, the reaction temperature is 65 °C，and the reaction time is 3h ; the second step, KOH is used as catalyst, the amount of the KOH is 0.15wt%, the levels of methanol to oil ratio is 25:1, reaction temperature is 60 °C， reaction time is 1h. The maximum yield of biodiesel is 93.24wt%.

Synthesis and Characterization of Heterogeneous Solid Acid Catalyst from Alstonia Scolaris Stalks for Biodiesel Production using Waste Cooking Oil

2020 ◽  
Vol 10 ◽  
Author(s):  
Charishma Venkata Sai Anne ◽  
Karthikeyan S. ◽  
Arun C.
Keyword(s):  
Reaction Time ◽  
Solid Acid ◽  
Solid Acid Catalyst ◽  
Acid Catalyst ◽  
Waste Cooking Oil ◽  
Biodiesel Production ◽  
Wood Biomass ◽  
Waste Wood ◽  
X Ray ◽  
Cooking Oil

Background: Waste biomass derived reusable heterogeneous acid based catalysts are more suitable to overcome the problems associated with homogeneous catalysts. The use of agricultural biomass as catalyst for transesterification process is more economical and it reduces the overall production cost of biodiesel. The identification of an appropriate suitable catalyst for effective transesterification will be a landmark in biofuel sector Objective: In the present investigation, waste wood biomass was used to prepare a low cost sulfonated solid acid catalyst for the production of biodiesel using waste cooking oil. Methods: The pretreated wood biomass was first calcined then sulfonated with H2SO4. The catalyst was characterized by various analyses such as, Fourier-transform infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDS) and X-ray diffraction (XRD). The central composite design (CCD) based response surface methodology (RSM) was applied to study the influence of individual process variables such as temperature, catalyst load, methanol to oil molar ration and reaction time on biodiesel yield. Results: The obtained optimized conditions are as follows: temperature (165 ˚C), catalyst loading (1.625 wt%), methanol to oil molar ratio (15:1) and reaction time (143 min) with a maximum biodiesel yield of 95 %. The Gas chromatographymass spectrometry (GC-MS) analysis of biodiesel produced from waste cooking oil was showed that it has a mixture of both monounsaturated and saturated methyl esters. Conclusion: Thus the waste wood biomass derived heterogeneous catalyst for the transesterification process of waste cooking oil can be applied for sustainable biodiesel production by adding an additional value for the waste materials and also eliminating the disposable problem of waste oils.

Production of Biodiesel from Waste Cooking Oil via Ultrasonic-Assisted Catalytic System

2014 ◽  
Vol 699 ◽  
pp. 552-557 ◽  
Author(s):  
Norzita Ngadi ◽  
Lai Nyuk Ma ◽  
Hajar Alias ◽  
Anwar Johari ◽  
Roshanida Abd Rahman ◽  
...  
Keyword(s):  
Calcium Oxide ◽  
Catalyst Concentration ◽  
Waste Cooking Oil ◽  
Molar Ratio ◽  
Catalyst Amount ◽  
Cooking Oil ◽  
Used Oil ◽  
Ultrasonic Assisted ◽  
Transesterification Method ◽  
Percentage Conversion

In this study, production of biodiesel from waste cooking oil (WCO) was carried out via ultrasonic-assisted transesterification method. Calcium oxide (CaO) was used as a catalyst. The effects of methanol to oil molar ratio, reaction temperature and the catalyst amount towards the percentage conversion of oil to biodiesel were investigated. The biodiesel produced was analyzed using GC-FID method. The results obtained showed that 82 % of oil was successfully converted into biodiesel. This indicates that the used oil (WCO) has the potential to be the future source of biodiesel. Catalyst concentration of 3 w/w%, methanol to oil molar ratio of 15:1 and temperature of 65°C are the best condition for the conversion of oil to biodiesel. The result obtained was found out that, methanol to oil molar ratio and catalyst amount has given significant effect on the conversion of oil. However, temperature ranged from (35 to 75) °C apparently, showed no significant effect on percentage conversion of oil.

scholarly journals Evaluation of Shell-Derived Calcium Oxide Catalysts for the Production of Biodiesel Esters from Cooking Oils

2021 ◽  
pp. 20-27
Author(s):  
Ngee Sing Chong ◽  
Francis Uchenna Okejiri ◽  
Saidi Abdulramoni ◽  
Shruthi Perna ◽  
Beng Guat Ooi
Keyword(s):  
Calcium Oxide ◽  
Waste Cooking Oil ◽  
Biodiesel Production ◽  
Molar Ratio ◽  
X Ray ◽  
Cooking Oil ◽  
Biodiesel Synthesis ◽  
Cooking Oils ◽  
The Cost ◽  
Percentage Conversion

Due to the high cost of feedstock and catalyst in biodiesel production, the viability of the biodiesel industry has been dependent on government subsidies or tax incentives. In order to reduce the cost of production, food wastes including eggshells and oyster shells have been used to prepare calcium oxide (CaO) catalysts for the transesterification reaction of biodiesel synthesis. The shells were calcined at 1000 °C for 4 hours to obtain CaO powders which were investigated as catalysts for the transesterification of waste cooking oil. The catalysts were characterized by Fourier Transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray powder diffraction (XRD), and X-ray fluorescence (XRF) spectroscopy. Reaction parameters such as methanol-to-oil molar ratio, CaO catalyst concentration, and reaction time were evaluated and optimized for the percentage conversion of cooking oil to biodiesel esters. The oyster-based CaO showed better catalytic activity when compared to the eggshell-based CaO under the same set of reaction conditions.

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