scholarly journals Preparation of Activated Carbons from Hydrolyzed Dipterocarpus alatus Leaves: Value Added Product from Biodiesel Production Waste

2021 ◽  
Vol 100 (10) ◽  
pp. 219-224
Author(s):  
Warangkana KHANGWICHIAN ◽  
Sudarat PATTAMASEWE ◽  
Atip LAUNGPHAIROJANA ◽  
Rattanaporn LEESING ◽  
Andrew J. HUNT ◽  
...  
RSC Advances ◽  
2016 ◽  
Vol 6 (51) ◽  
pp. 45419-45427 ◽  
Author(s):  
Mary K. S. Batista ◽  
Ana S. Mestre ◽  
Inês Matos ◽  
Isabel M. Fonseca ◽  
Ana P. Carvalho

Turning waste into valuable products: K2CO3 activation of rapeseed residues from biodiesel industry for the production of new and reusable activated carbons for caffeine removal from water.


Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 34
Author(s):  
Devendra P. Tekale ◽  
Ganapati D. Yadav ◽  
Ajay K. Dalai

Value addition to glycerol, the sole co-product in biodiesel production, will lead to reform of the overall biodiesel economy. Different valuable chemicals can be produced from glycerol using heterogeneous catalysis and these valuable chemicals are useful in industries such as cosmetics, pharmaceuticals, fuels, soap, paints, and fine chemicals. Therefore, the conversion of glycerol to valuable chemicals using heterogeneous catalysis is a noteworthy area of research. Etherification of glycerol with alkenes or alcohols is an important reaction in converting glycerol to various value-added chemicals. This article describes reaction of glycerol with benzyl alcohol in solvent-free medium by using a clay supported modified heteropolyacid (HPA), Cs2.5H0.5PW12O40/K-10 (Cs-DTP/K-10) as solid catalyst and its comparison with other catalysts in a batch reactor. Mono-Benzyl glycerol ether (MBGE) was the major product formed in the reaction along with formation of di-benzyl glycerol ether (DBGE). The effects of different parameters were studied to optimize the reaction parameters. This work provides an insight into characterization of Cs2.5H0.5PW12O40/K-10 catalyst by advanced techniques such as surface area measurement, X-ray analysis, ICP-MS, FT-IR, and SEM. Reaction products were characterized and confirmed by using the GCMS method. The kinetic model was developed from an insight into the reaction mechanism. The apparent energy of activation was found to be 18.84 kcal/mol.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Azhar Najjar ◽  
Elhagag Ahmed Hassan ◽  
Nidal Zabermawi ◽  
Saber H. Saber ◽  
Leena H. Bajrai ◽  
...  

AbstractIn this study, two highly thermotolerant and methanol-tolerant lipase-producing bacteria were isolated from cooking oil and they exhibited a high number of catalytic lipase activities recording 18.65 ± 0.68 U/mL and 13.14 ± 0.03 U/mL, respectively. Bacterial isolates were identified according to phenotypic and genotypic 16S rRNA characterization as Kocuria flava ASU5 (MT919305) and Bacillus circulans ASU11 (MT919306). Lipases produced from Kocuria flava ASU5 showed the highest methanol tolerance, recording 98.4% relative activity as well as exhibited high thermostability and alkaline stability. Under the optimum conditions obtained from 3D plots of response surface methodology design, the Kocuria flava ASU5 biocatalyst exhibited an 83.08% yield of biodiesel at optimized reaction variables of, 60 ○C, pH value 8 and 1:2 oil/alcohol molar ratios in the reaction mixture. As well as, the obtained results showed the interactions of temperature/methanol were significant effects, whereas this was not noted in the case of temperature/pH and pH/methanol interactions. The obtained amount of biodiesel from cooking oil was 83.08%, which was analyzed by a GC/Ms profile. The produced biodiesel was confirmed by Fourier-transform infrared spectroscopy (FTIR) approaches showing an absorption band at 1743 cm−1, which is recognized for its absorption in the carbonyl group (C=O) which is characteristic of ester absorption. The energy content generated from biodiesel synthesized was estimated as 12,628.5 kJ/mol. Consequently, Kocuria flava MT919305 may provide promising thermostable, methanol-tolerant lipases, which may improve the economic feasibility and biotechnology of enzyme biocatalysis in the synthesis of value-added green chemicals.


2010 ◽  
Vol 658 ◽  
pp. 73-76
Author(s):  
Yotwadee Hawangchu ◽  
Duangduen Atong ◽  
Viboon Sricharoenchaikul

Glycerol waste is by-product from the manufacturing of biodiesel by transesterification method containing impurities such as fatty acid, alcohol, spent catalyst, soap and water. Conversion of this waste to value added fuel products would not only improve economic of biodiesel production but also reduce environmental impact from this process. In this work, thermal conversion of glycerol waste by microwave that induced the heat required for initiating the reaction was carried out in a fixed bed quartz reactor using silicon carbide as the bed medium for microwave receptor as well as supporter for nickel catalyst. For non-catalytic reaction at 220W (700°C), carbon and hydrogen conversions were 22.89% and 19.59%, respectively. Gas production was 0.12 L/min syngas, 0.07 L/min H2, 0.82 MJ/m3 of LHV, and 1.27 H2/CO. In catalytic test, the highest syngas, H2, and LHV of 0.41 L/min, 0.23 L/min, and 9.18 MJ/m3, respectively, were obtained from 1%Ni/SiC while the highest H2/CO of 2.72 was obtained from 0.5%Ni/SiC. The 1%Ni/SiC test also resulted in the highest conversion of carbon and hydrogen as much as 79.50% and 83.26%, respectively. For comparison between fresh and regenerated catalysts, it was found that fresh catalyst performed significantly better that regenerated one in term of higher total conversion which may due to sodium deposition on spent catalyst surface.


Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 373 ◽  
Author(s):  
Mattia Bartoli ◽  
Chengyong Zhu ◽  
Michael Chae ◽  
David Bressler

Although thermal hydrolysis of digested biosolids is an extremely promising strategy for wastewater management, the process economics are prohibitive. Here, a biosolids-based material generated through thermal hydrolysis was used as a catalyst for urea glycerolysis performed under several conditions. The catalytic system showed remarkable activity, reaching conversion values of up to 70.8 ± 0.9% after six hours, at 140 °C using a catalyst/glycerol weight ratio of 9% and an air stream to remove NH3 formed during the process. Temperature played the most substantial role among reaction parameters; increasing temperature from 100 °C to 140 °C improved conversion by 35% and glycidol selectivity by 22%. Furthermore, the catalyst retained good activity even after the fourth catalytic run (conversion rate of 56.4 ± 1.3%) with only a slight decrease in glycidol selectivity. Thus, the use of a biosolids-based catalyst may facilitate conversion of various glycerol sources (i.e., byproduct streams from biodiesel production) into value-added products such as glycidol, and may also improve the economic feasibility of using thermal hydrolysis for treatment of biosolids.


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 609 ◽  
Author(s):  
Niravkumar Mahendrasinh Kosamia ◽  
Mahdieh Samavi ◽  
Bijaya Kumar Uprety ◽  
Sudip Kumar Rakshit

The rapid growth of global biodiesel production requires simultaneous effective utilization of glycerol obtained as a by-product of the transesterification process. Accumulation of the byproduct glycerol from biodiesel industries can lead to considerable environment issues. Hence, there is extensive research focus on the transformation of crude glycerol into value-added products. This paper makes an overview of the nature of crude glycerol and ongoing research on its conversion to value-added products. Both chemical and biological routes of glycerol valorization will be presented. Details of crude glycerol conversion into microbial lipid and subsequent products will also be highlighted.


2020 ◽  
Vol 7 (3) ◽  
pp. 259-266
Author(s):  
Xue-Lian Li ◽  
Quan Zhou ◽  
Shen-Xi Pan ◽  
Yu He ◽  
Fei Chang

: Glycerol is an organic polyol compound, and is an important raw material with extensive applications in daily/petrochemical and pharmaceutical industry. Glycerol is typically obtained by propylene chlorination, while the method used is complicated process and requires high energy consumption. Interestingly, glycerol is recognized as a major by-product of biodiesel production. Approximately 100 kg of glycerol is yielded for 1 tonne of biodiesel production. With the rapid development of the biodiesel industry, glycerol production capacity has been a serious surplus. This review introduces the selective conversion of glycerol into a variety of value-added chemicals such as propylene glycol, propanol, glyceraldehyde, and dihydroxyacetone via selective hydrogenation and oxidation, as well as hydrocarbons and ethers via pyrolysis, gasification and etherification, respectively. The efficiency of different types of catalysts and the influence of reaction parameters on the valorisation of glycerol have been elucidated. Emphasis is also laid on the study of catalytic mechanisms and pathways for some specific reactions.


2009 ◽  
Vol 100 (5) ◽  
pp. 1786-1792 ◽  
Author(s):  
Anne A. Nunes ◽  
Adriana S. Franca ◽  
Leandro S. Oliveira

Author(s):  
Duangduen Atong ◽  
Viboon Sricharoenchaikul

Thermochemical conversion process has become a viable technology for managing excess waste from various industries while producing value added fuel products. In the work reported here, distribution of products (solid, liquid, and gas) by thermal conversion of wastes from biodiesel production process which are extracted physic nut and palm shell mixed with glycerol waste was carried out using a medium scale tubular reactor with feeding rate of 5 g/min. Several important operating parameters were studied including the proportion of each waste (100:0 – 70:30), reaction temperature (700 – 900°C) and air to fuel ratio (AF) 0.0 – 0.6. It was found that when the temperature increased, the quantity of solid and liquid product decreased while gas product increased. For conversion to CO2, CO, CxHy and H2, when the temperature increased, CO2 decreased while yields of CO, CH4 and H2 increased. Greater conversion to CO2, CO, H2 with AF increased from 0.0 to 0.3. Higher AF from 0.3 to 0.6 resulted in lesser CO and H2 while conversion to CO2 increased. On the other hand, CxHy decreased when AF changed from 0.0 to 0.6. The maximum heating values of gas product in this study are 3.48 MJ/m3 and 2.27 MJ/m3 for glycerol waste mixed with physic nut waste and palm shell waste, respectively (both at 30% glycerol wastes and reaction temperature of 900°C). The maximum of mole ratio of H2 to CO obtained is 0.59 for physic nut and 0.37 for palm shell mixed wastes. Relatively high CxHy, low product gas heating value and H2 to CO ratio indicated the need for further product upgrading before using as raw material for other advanced fuel production processes such as Fisher-Tropsch, DME, or methanol syntheses beside direct heat and power utilization.


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