以 Zr 基 MOF 为支撑固定脂肪酶,增强生物柴油生产中的酶促酯交换反应

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2024-10-09 DOI:10.1016/j.mcat.2024.114603
Xiangsheng Zheng, Xiaohong Hao, Yan Wang, Siyu Gao, Dantong Wen, Jinchuan Wang
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引用次数: 0

摘要

开发新型生物催化剂对于促进通过酯交换反应生产生物柴油的商业化至关重要。本文通过界面吸附法将根瘤菌脂肪酶(ROL)固定在氨基功能化的锆基金属有机骨架上。对固定化条件进行了优化,并测试了酶的特性,结果表明新型生物催化剂具有更高的稳定性和耐热性。利用 SEM、XRD 和 BET 分析了生物催化剂和载体材料的特性。探讨了 ROL@UiO-66-NH2 在酯交换反应生产生物柴油过程中的催化性能,并采用响应面法对生产工艺进行了优化。结果表明,在乙醇/油摩尔比为 15.43:1、反应温度为 50.28°C、反应时间为 120.9 分钟、DES 添加量为 48.08 wt%、生物催化剂添加量为 3 wt%、超声功率为 90 W 的条件下,FAEE 的转化率达到 82.05%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Zr-based MOF as a support for lipase immobilization to enhance enzymatic transesterification for biodiesel production
The development of novel biocatalysts is essential to promote the commercialization of biodiesel production by transesterification reaction. In this paper, Rhizopus oryzae lipase (ROL) was immobilized on an amino-functionalized zirconium-based metal organoskeleton by interfacial adsorption. The immobilization conditions were optimized and the enzymatic properties were tested, and the resulting novel biocatalysts exhibited higher stability and heat resistance. SEM, XRD and BET analyses were used to characterize the biocatalysts and carrier materials. The catalytic performance of ROL@UiO-66-NH2 in the production of biodiesel by transesterification reaction was explored, and the production process was optimized by response surface method. The results showed that the conversion rate of FAEE reached 82.05% at molar ratio of ethanol/oil of 15.43:1, reaction temperature of 50.28°C, reaction time of 120.9 min, DES addition of 48.08 wt%, biocatalyst addition of 3 wt%, and ultrasonic power of 90 W. In addition, ROL@UiO-66-NH2 demonstrated good recyclability, with the catalytic efficiency remaining at 71.87% after five cycles.
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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