Functionalized polyacrylonitrile nanofiber membranes with carbonic anhydrase for enhanced carbon dioxide capture and conversion: A performance study

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biochemical Engineering Journal Pub Date : 2024-11-13 DOI:10.1016/j.bej.2024.109570
Shen-Yuan Yang , Jia-Yih Lin , Pei-Rong Li , Nguyen The Duc Hanh , Penjit Srinophakun , Bing-Lan Liu , Chen-Yaw Chiu , I-Son Ng , Kuei-Hsiang Chen , Yu-Kaung Chang
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Abstract

As industrial activity rises, atmospheric carbon dioxide levels have significantly contributed to global warming and climate change. Developing effective carbon dioxide capture technologies is imperative to mitigate these effects. Carbonic anhydrase (CA) enzymes represent one of the most promising solutions due to their rapid reaction rates, environmental safety, and efficiency in facilitating CO2 conversion. This study takes a novel approach by investigating the immobilization of CA on functionalized polyacrylonitrile (PAN) nanofiber membranes to enhance CO2 conversion and mineralization. PAN nanofibers were fabricated via electrospinning and chemically modified to introduce carboxylic groups, resulting in NM-COOH nanofiber membranes. In addition, amine groups from chitosan (CS) were incorporated to form NM-COOH-CS nanofiber membranes. The immobilization of CA on these membranes revealed that covalent attachment through NM-COOH significantly enhances catalytic activity compared to physical attachment methods. The NM-COOH-CA membrane exhibited superior performance, achieving efficient conversion of CO2 into HCO3 and promoting CaCO3 mineralization. It reached a precipitation efficiency of 11.77 mg CaCO3 per gram of membrane-active unit (WAU) and maintained 63.12 % of its initial CaCO3 production over five cycles over five weeks. This study presents a novel, eco-friendly approach to greenhouse gas reduction, emphasizing the effectiveness of CA-immobilized nanofiber membranes. The findings mainly highlight the advantages of carboxylic functional groups in enhancing CA performance, paving the way for future research in carbon capture technologies.
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含碳酸酐酶的功能化聚丙烯腈纳米纤维膜,用于增强二氧化碳捕获和转化:性能研究
随着工业活动的增加,大气中的二氧化碳含量大大加剧了全球变暖和气候变化。为减轻这些影响,开发有效的二氧化碳捕获技术势在必行。碳酸酐酶(CA)因其快速的反应速度、环境安全性和促进二氧化碳转化的效率而成为最有前途的解决方案之一。本研究采用一种新方法,研究如何将碳酸酐酶固定在功能化聚丙烯腈(PAN)纳米纤维膜上,以提高二氧化碳的转化和矿化。通过电纺丝制造 PAN 纳米纤维,并对其进行化学改性以引入羧基,从而制成 NM-COOH 纳米纤维膜。此外,还加入了壳聚糖(CS)中的胺基团,形成了 NM-COOH-CS 纳米纤维膜。将 CA 固定在这些膜上的结果表明,与物理附着方法相比,通过 NM-COOH 进行共价附着能显著提高催化活性。NM-COOH-CA 膜性能优越,能将 CO2 高效转化为 HCO3-,并促进 CaCO3 矿化。它的沉淀效率达到每克膜活性单元(WAU)11.77 毫克 CaCO3,并在五周的五个循环中保持了其初始 CaCO3 产量的 63.12%。这项研究提出了一种减少温室气体的新型环保方法,强调了 CA 固定化纳米纤维膜的有效性。研究结果主要强调了羧基官能团在提高 CA 性能方面的优势,为未来碳捕集技术的研究铺平了道路。
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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