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首页> 外文期刊>Asian Journal of Microbiology, Biotechnology and Environmental Science >KINETIC ANALYSIS OF FATTY ACID ALKYL ESTERS USING WHOLE CELL BIOCATALYST AND LIPASE CATALYZED TRANSESTERIFICATION FROM WASTE COOKING OIL
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KINETIC ANALYSIS OF FATTY ACID ALKYL ESTERS USING WHOLE CELL BIOCATALYST AND LIPASE CATALYZED TRANSESTERIFICATION FROM WASTE COOKING OIL

机译:废烹饪油中全细胞生物催化剂和脂酶催化的酯交换反应动力学分析脂肪酸烷基酯

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摘要

In the present scenario of energy crisis and depleting fossil fuels, there is a need for alternative fuels such as biodiesel. Waste cooking oil, a kitchen waste was analyzed as a potential source for biodiesel production by transesterification using four different acyl acceptors-Methanol, Iso-propanol, Iso-butanol and Iso-amyl Alcohol in a solvent free system. In the present work transesterification was carried out using biocatalysts- lipase enzyme in purified form and as whole cell biocatalyst of filamentous fungi Rhizopus oryzae. First, an optimization of the reaction conditions and comparative analysis of the yields for both the catalyst was obtained. During our further study, a kinetic study for the enzyme catalyzed and whole cell catalyzed process was developed using Ping-pong Bi-Bi Kinetics model with substrate competitive inhibition. Among the different acyl acceptors, methanol whose reaction parameters were optimized as 35°C, 1:3 (oil/alcohol), 24h, 150rpm and 10% lipase concentration (mass ratio to oil) showed maximum conversion of triglycerides to Biodiesel - 94% with Purified Enzyme and 84% with Whole Cell Biocatalyst. Kinetic model based Ping-pong Bi-Bi model with competitive substrate inhibition by alcohol was used to find the maximum reaction rate Vi for the four acyl acceptors using pure enzyme and Whole Cell Biocatalyst. The results showed the initial rate of reation was lower for whole cell biocatalyst which was mainly due to the reduced substrate diffusion through the cell membrane and this observation can be also supported by the fact that whole cell biocatalyst remained stable for longer time due to the reduced inhibitor exposure.
机译:在当前的能源危机和化石燃料枯竭的情况下,需要替代燃料,例如生物柴油。在无溶剂系统中,通过使用四种不同的酰基受体(甲醇,异丙醇,异丁醇和异戊醇)进行酯交换反应,分析了厨用废油和厨余作为生物柴油生产的潜在来源。在本工作中,使用纯化形式的生物催化剂-脂肪酶作为丝状真菌米根霉的全细胞生物催化剂进行酯交换反应。首先,获得了两种催化剂的反应条件的优化和收率的对比分析。在我们的进一步研究中,使用具有底物竞争抑制作用的乒乓Bi-Bi动力学模型,对酶催化和全细胞催化过程进行了动力学研究。在不同的酰基受体中,反应参数最优化为35°C,1:3(油/醇),24h,150rpm和10%脂肪酶浓度(与油的质量比)的甲醇显示出甘油三酸酯向生物柴油的最大转化率-94%含纯化的酶和84%的全细胞生物催化剂。使用基于动力学模型的具有竞争性底物被酒精抑制的乒乓Bi-Bi模型,使用纯酶和全细胞生物催化剂来找到四个酰基受体的最大反应速率Vi。结果表明,全细胞生物催化剂的初始反应速率较低,这主要是由于底物在细胞膜中的扩散减少所致,而这种观察结果也可以得到以下事实的支持:全细胞生物催化剂由于还原而在更长的时间内保持稳定抑制剂暴露。

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