2010
DOI: 10.1016/j.cej.2009.12.037
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Biodiesel production from crude palm oil using sulfonic acid-modified mesostructured catalysts

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Cited by 178 publications
(92 citation statements)
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“…In the case of sulfonated carbons, deactivation has been attributed to leaching of soluble polycyclic aromatics with sulfonic groups [14,33], simple physical loss of catalyst [15], or hydrolysis of sulfonic groups [34]. Other acid catalysts have also shown a similar behaviour with respect to stability in esterification reactions, that have been explained by leaching problems in sulfated zirconia [35], hydrocarbon accumulation in SAC-13 [36] and organosulfonic silica [37], and several reasons, including leaching of sulfonic species, water and glycerol adsorption, and even reaction with methanol in the case of sulfonic-acid modified SBA-15 [38,39].…”
Section: Introductionmentioning
confidence: 95%
See 1 more Smart Citation
“…In the case of sulfonated carbons, deactivation has been attributed to leaching of soluble polycyclic aromatics with sulfonic groups [14,33], simple physical loss of catalyst [15], or hydrolysis of sulfonic groups [34]. Other acid catalysts have also shown a similar behaviour with respect to stability in esterification reactions, that have been explained by leaching problems in sulfated zirconia [35], hydrocarbon accumulation in SAC-13 [36] and organosulfonic silica [37], and several reasons, including leaching of sulfonic species, water and glycerol adsorption, and even reaction with methanol in the case of sulfonic-acid modified SBA-15 [38,39].…”
Section: Introductionmentioning
confidence: 95%
“…Both effects may be due either to a strong physisorption of molecular methanol by formation of hydrogen bonds with the highly oxygenated structure of the hydrothermal carbon or to chemical reaction of methanol with some sulfonic groups leading to surface methyl sulfonates. Some authors have proposed this possibility in the deactivation of mesoporous silicas modified with sulfonic groups [38,39], but without experimental evidences.…”
Section: Nmr Study Of Deactivated Catalystsmentioning
confidence: 99%
“…Para sanar as limitações da transesterificação básica homogênea, poder-se-ia produzir biodiesel por catálise homogênea ácida utilizando um ácido forte de Brönsted (doador de prótons), no entanto essa rota reacional é menos lenta em comparação à rota básica, diminui o rendimento de biodiesel, além de causar corrosão dos equipamentos. 4,8,9 A adequação de matérias-primas oleaginosas de baixa qualidade, ou seja, contendo elevado índice de acidez e elevado teor de água na obtenção sustentável de biodiesel, é de fundamental importân-cia. Estes insumos energéticos, se tratados adequadamente, podem contribuir de forma positiva para a preservação ambiental e redução do custo do processo reacional de transesterificação, tornando o biodiesel mais competitivo em comparação ao diesel de petróleo.…”
Section: Introductionunclassified
“…Em geral, uma esterificação prévia é necessária, de forma a diminuir a concentração de ácidos graxos livres e permitir a posterior transesterificação básica da matéria-prima. 8,9 Os AGL reagem com a água na presença do catalisador alcalino, formando sais de ácidos graxos que dificultam a separação, lavagem e purificação do biodiesel. No final da rota reacional por transesterificação homogênea básica obtém-se duas fases distintas, uma menos densa contendo os monoésteres e uma fase mais densa contendo o glicerol.…”
unclassified
“…The most widely used method for biodiesel production in industrial scale is conventional method using homogeneous and heterogeneous catalysts, either acid or base catalysts [2][3][4][5][6][7][8][9]. However, the conventional catalytic reaction technology is considered inefficient because of the length of time the reaction and batch time and some separation processes.…”
Section: Introductionmentioning
confidence: 99%