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首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Synthesis of butyl butyrate in batch and continuous enzymatic reactors using Thermomyces lanuginosus lipase immobilized in Immobead 150
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Synthesis of butyl butyrate in batch and continuous enzymatic reactors using Thermomyces lanuginosus lipase immobilized in Immobead 150

机译:使用固定在Immobead 150中的羊毛嗜热霉脂肪酶在间歇和连续酶反应器中合成丁酸丁酯

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Thermomyces lanuginosus lipase (TLL) was covalently immobilized on Immobead 150 (ImmTLL) via epoxy groups of the support and the lysine of the enzyme to be used in the synthesis of butyl butyrate. The optimization of the esterification reaction parameters was carried out by central composite design and response surface methodology, having product yield as target, with all tested variables showing to be statistically significant on the conversion. The optimal conditions for butyl butyrate synthesis were: temperature of 40 degrees C, substrate molar ratio of 3:1 butanol:butiric acid, 40% of enzyme amount in relation to substrate weight, and 2.5% of water (volume fraction of reaction), using hexane as solvent. Under these conditions, over 84% of conversion was obtained after 4h of reaction in a batch reactor, with a productivity of 0.27 mmol g(-1) h(-1) per gram of derivative. The butyl butyrate synthesis was also evaluated in a continuous reactor, using two configurations: packed-bed reactor (PBR) and fluidized-bed reactor (FBR). The highest productivity per gram of derivative in the continuous process was 1.01 mmol g(-1) h(-1), reached using the PBR containing 1.5 g of ImmTLL and glass beads. The biocatalyst presented operational stability at 40 degrees C, maintaining 83% of its initial conversion capacity after 8 cycles of reuse in batch reactor and 63% after 30 days of continuous operation in the PBR, using a flow rate of 0.02 mL min(-1). These results suggest that this immobilized system can be successfully used to produce butyl butyrate for food, cosmetics, and for pharmaceutical applications. (C) 2016 Elsevier B.V. All rights reserved.
机译:羊毛热霉菌脂肪酶(TLL)通过支持物的环氧基和赖氨酸的赖氨酸共价固定在Immobead 150(ImmTLL)上,用于丁酸丁酯的合成。酯化反应参数的优化是通过中央复合设计和响应面方法进行的,以产物收率为目标,所有测试变量在转化率上均具有统计学意义。合成丁酸丁酯的最佳条件是:温度为40摄氏度,底物摩尔比为3:1丁醇:丁酸,相对于底物重量而言40%的酶量,以及2.5%的水(反应体积分数),使用己烷作为溶剂。在这些条件下,在间歇式反应器中反应4小时后,可获得84%以上的转化率,每克衍生物的生产率为0.27 mmol g(-1)h(-1)。还使用两种配置在连续反应器中评估丁酸丁酯的合成:填充床反应器(PBR)和流化床反应器(FBR)。使用包含1.5 g ImmTLL和玻璃珠的PBR,在连续过程中,每克衍生物的最高生产率为1.01 mmol g(-1)h(-1)。该生物催化剂在40°C时表现出运行稳定性,在分批反应器中重复使用8个循环后保持其初始转化能力的83%,在PBR中连续运行30天后保持6%的初始转化能力,流速为0.02 mL min(-1 )。这些结果表明,该固定化系统可以成功地用于生产食品,化妆品和药物应用中的丁酸丁酯。 (C)2016 Elsevier B.V.保留所有权利。

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