Microwave assisted esterification of free fatty acid over a heterogeneous catalyst for biodiesel production

[Display omitted] •Microwave assisted esterification of stearic acid with ethanol was catalyzed by D418.•D418 exhibited remarkable catalytic performance for ethyl stearate formation.•It proved possible to prepare biodiesel rapidly and with good conversions by microwave heating.•The relative catalyti...

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Veröffentlicht in:Energy conversion and management 2013-12, Vol.76, p.1009-1014
Hauptverfasser: Liu, Wei, Yin, Ping, Liu, Xiguang, Chen, Wen, Chen, Hou, Liu, Chunping, Qu, Rongjun, Xu, Qiang
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Sprache:eng
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Zusammenfassung:[Display omitted] •Microwave assisted esterification of stearic acid with ethanol was catalyzed by D418.•D418 exhibited remarkable catalytic performance for ethyl stearate formation.•It proved possible to prepare biodiesel rapidly and with good conversions by microwave heating.•The relative catalytic kinetics study has been conducted and modeled. Biodiesel fuel is gaining significant attention in recent years because of its environmental benefits and the growing interest in finding new resources and alternatives for conventional fuels. Biodiesel production from waste cooking oil with high free fatty acids usually requires esterification step to produce fatty acid methyl/ethyl ester. In the present work, the heterogeneous catalyst aminophosphonic acid resin D418 has been successfully utilized in the energy-efficient microwave-assisted esterification reaction of fatty acid ethyl ester (FAEE) from free fatty acid (FFA) stearic acid with short-chain alcohol ethanol. Under the reaction conditions of 9wt% D418 and 11: 1M ratio of ethanol to stearic acid at 353K and atmospheric pressure, more than 90% conversion of the esterification was achieved in 7h by microwave heating, while it took about 12h by conventional heating. Moreover, the kinetics of this esterification reaction has been studied, and the relevant values of activation energy and pre-exponential factor were obtained.
ISSN:0196-8904
1879-2227
DOI:10.1016/j.enconman.2013.08.051