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Preparation and decontamination performance of a flexible self-standing hydrogel photocatalytic membrane

光催化 材料科学 化学工程 石墨氮化碳 可见光谱 氮化碳 催化作用 纳米技术 化学 有机化学 光电子学 生物化学 工程类
作者
Mengyang Lu,Hanmin Zhang
出处
期刊:Journal of Membrane Science [Elsevier]
卷期号:644: 119979-119979 被引量:25
标识
DOI:10.1016/j.memsci.2021.119979
摘要

The membrane immobilization of photocatalyst is a kind of win-win mode which can not only avoid the loss of catalyst but also give the membrane antibacterial and self-cleaning properties. Nevertheless, the inefficiency and low durability remain two major obstacles to hinder its practical applications. Herein, a facile micro-solvent combustion synthesis (MSCS) and sodium alginate (SA) crosslinking method were proposed to fabricate an integrated and self-standing membrane of nano-ZnCeOx combined with porous graphitic carbon nitride ([email protected]). In the photocatalytic-membrane separation system, the water flux of [email protected] was 800 l m−2•h−1•bar−1. Remarkably, the separation efficiency of [email protected] could reach more than 90% during the 4-h continuous membrane separation process. The water flux of [email protected] under visible light decreased only 21% which was less than that in the absence of light (53%), and the original flux could be completely restored after photocatalysis, signifying that the prepared [email protected] had good self-cleaning ability in membrane separation. Meanwhile, [email protected] exhibited 99% removal efficiency and 0.06131 min−1 reaction rate in photocatalysis experiments under 1-h visible light. The removal efficiency of [email protected] was 1.2-fold and 2.8-fold that of carbon nitride particles (CN) and hydrogel membrane morphology (CNM), respectively. The optical properties test of [email protected] showed that its excellent photocatalytic activity was derived from the rapid electron transfer caused by cross-linked structure, heterojunction and the oxygen vacancies induced by nano-ZnCeOx. The radical quenching experiment and EPR experiment showed that •O2− and •OH both were the main factors in reaction.

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