Bactericidal and biocatalytic temperature responsive microgel based self-cleaning membranes for water purification

漆酶 甲基丙烯酸缩水甘油酯 化学工程 共价键 固定化酶 化学 材料科学 嫁接 壳聚糖 渗透 热稳定性 高分子化学 聚合物 有机化学 单体 生物化学 工程类
作者
Supriya Maity,Divya Gaur,Biswajit Mishra,Nidhi C. Dubey,Bijay P. Tripathi
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:642: 129-144 被引量:14
标识
DOI:10.1016/j.jcis.2023.03.095
摘要

The present study focuses on creating an antimicrobial and biocatalytic smart gating membrane by synthesizing unique core–shell microgels. The core–shell microgels are synthesized by grafting short chains of poly(ethylenimine) (PEI) onto a poly((N-isopropyl acrylamide)–co-glycidyl methacrylate)) (P(NIPAm-co-GMA)) core. Subsequently, the produced microgels are utilized as a substrate for synthesizing and stabilizing silver nanoparticles (Ag NPs) through an in-situ approach. These Ag NPs immobilized microgels are then suction filtered over a polyethylene terephthalate (PET) track-etched support to create cross-linked composite microgel membranes (CMMs). After structural and permeation characterization of the prepared CMMs, the laccase enzyme is then covalently grafted to the surface of the membrane and tested for its effectiveness in degrading Reactive red-120 dye. The laccase immobilized biocatalytic CMMs show effective degradation of the Reactive red-120 by 71%, 48%, and 34% at pH 3, 4, and 5, respectively. Furthermore, the immobilized laccase enzyme showed better activity and stability in terms of thermal, pH, and storage compared to the free laccase, leading to increased reusability. The unique combination of Ag NPs and laccase on a thermoresponsive microgel support resulted in a responsive self-cleaning membrane with excellent antimicrobial and dye degradation capabilities for environmentally friendly separation technology.
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