Preparation of defective UiO-67 for CA immobilization to improve the ability of CO2 capture and conversion

被引:0
|
作者
Zhao, Rui [1 ]
Yang, Wenhui [1 ]
Yang, Pengyan [1 ]
Cao, Yunhan [1 ]
Wang, Fenghuan [1 ]
机构
[1] Beijing Technol & Business Univ BTBU, Sch Light Ind Sci & Engn, Beijing 100048, Peoples R China
关键词
Metal-organic frameworks; Defective engineering; Carbonic anhydrase; CO; 2; conversion; METAL-ORGANIC FRAMEWORK; BOVINE CARBONIC-ANHYDRASE; BIOMIMETIC SEQUESTRATION; COVALENT IMMOBILIZATION; SELECTIVE ADSORPTION; MODULATED SYNTHESIS; ENZYME; MOFS; LIPASE; HYBRID;
D O I
10.1016/j.bej.2025.109661
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Carbonic anhydrase (CA) has been suggested as a biocatalyst for carbon dioxide capture since it could effectively catalyze the hydration of carbon dioxide. Metal-organic frameworks (MOFs) have attracted significant attention in the development of immobilized enzyme carriers due to their pore tunability and excellent stability. In this study, UiO-67 materials with varying defect degrees (DUiO-67) were prepared using the organic linker missing method to enhance the catalytic performance. The results indicated that both the defect degree and the pore size of DUiO-67 materials decreased with an increase in acetic acid equivalent. After CA immobilization, all DUiO-67 materials exhibited excellent thermal, pH and recycling stability. CA@DUiO-67-25 showed higher enzyme catalytic activity and conversion ability than the other materials. After 10 cycles, CA@DUiO-67-25 retained 57 % of its initial conversion capacity. The construction of defective MOFs provides a promising new strategy for CA immobilization to achieve the catalytic conversion of CO2.
引用
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页数:11
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