Carbonic Anhydrase‐Embedded Hydrogen‐Bonded Organic Frameworks Coating for Facilitated Offshore CO2 Fixation

催化作用 碳酸酐酶 化学 涂层 海水 固碳 化学工程 矿化(土壤科学) 二氧化碳 环境化学 有机化学 氮气 工程类 海洋学 地质学
作者
Bo‐Yu Zhang,Wei Xing Zheng,Ziyi Chu,Ké Li,Jiafu Shi
出处
期刊:ChemBioChem [Wiley]
卷期号:24 (10) 被引量:3
标识
DOI:10.1002/cbic.202300114
摘要

Exhausted emission of carbon dioxide (CO2 ) from ships or offshore platforms has become one of the major contributors to global carbon emissions. Enzymes such as carbonic anhydrase (CA) have been widely used for CO2 mineralization because of their high catalytic rate. However, CA in seawater is easy to inactivate and difficult to reuse. Immobilization would be a feasible solution to address the stability issue, which, however, may cause an increase of internal diffusion resistance and reduced catalytic activity. In this regard, design of high-performance biocatalysts for acquiring high catalytic activity and stability of CA is highly desirable. Herein, a monolithic catalyst of Filler-CA@Lys-HOF-1 (FCLH) was prepared by chemical sorption of CA on the surface of the Filler followed by the coating of Lys-HOF-1. The highest catalytic activity of FCLH was obtained by regulating the amount of HOF-1 monomer added. Due to the protection of Lys-HOF-1, the FCLH showed good tolerance against acidity and salinity, which could retain about 80.2 % of the original activity after 9 h incubation in simulated seawater. The catalytic activity of FCLH could retain 85.4 % of the initial activity after 10 cycles. Hopefully, our study can provide a promising biocatalyst for CO2 mineralization, which may drive down carbon emissions when used for CO2 capture and conversion on offshore platforms.
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