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新型g-CN@膨胀石墨的简便组装及纳米零价铁的表面负载用于增强四环素的协同降解

Facile assembly of novel g-CN@expanded graphite and surface loading of nano zero-valent iron for enhanced synergistic degradation of tetracycline.

作者信息

Wang Xiangyu, Xie Yu, Ma Jun, Ning Ping

机构信息

Faculty of Environmental Science and Engineering, Kunming University of Science and Technology Kunming 650500 China

State Key Laboratory of Urban Water Resources and Environment, Harbin Institute of Technology Harbin 150090 China.

出版信息

RSC Adv. 2019 Oct 28;9(59):34658-34670. doi: 10.1039/c9ra06620a. eCollection 2019 Oct 23.

Abstract

The two-stage removal process of tetracycline (TC) in aqueous solutions using a novel photocatalyst based on nano-zero-valent iron (NZVI), g-CN and expanded graphite by carbon layer (EGC) is reported for the first time. The composite (NZVI/g-CN@EGC) exhibits remarkable adsorption, reduction ability and visible light activity over the reaction course. Compared with pristine g-CN (25.9%) and pure NZVI (45.9%), NZVI/g-CN@EGC achieves high degradation efficiency of TC (98.5%) due to the formation of a heterogeneous photo-Fenton system. This study shows that synergistic effects are achieved in the reaction system, including maintaining the reduction ability of NZVI and enhancing the photocatalytic activity of g-CN by facilitating the separation of photogenerated electrons (e) and holes (h). TC removal involved a two-stage process of adsorption-reduction and photo-degradation. The quencher experiments determined that holes (h) and superoxide radicals (˙O ) are the major reactive species in the degradation of TC. The degradation pathways of TC were proposed based on the analysis of the intermediates. In addition, NZVI/g-CN@EGC revealed a high stability in a five-cycle test and good magnetic properties for facile separation from aqueous solutions. From an application viewpoint, NZVI/g-CN@EGC has favorable prospects in the direction of the photocatalytic degradation of antibiotic wastewater.

摘要

首次报道了使用基于纳米零价铁(NZVI)、石墨相氮化碳(g-CN)和碳层膨胀石墨(EGC)的新型光催化剂对水溶液中的四环素(TC)进行两步去除过程。在整个反应过程中,复合材料(NZVI/g-CN@EGC)表现出显著的吸附、还原能力和可见光活性。与原始g-CN(25.9%)和纯NZVI(45.9%)相比,由于形成了异质光芬顿体系,NZVI/g-CN@EGC实现了对TC的高效降解(98.5%)。该研究表明,反应体系中实现了协同效应,包括维持NZVI 的还原能力以及通过促进光生电子(e)和空穴(h)的分离来增强g-CN的光催化活性。TC的去除涉及吸附-还原和光降解两个阶段的过程。猝灭实验确定空穴(h)和超氧自由基(˙O )是TC降解过程中的主要活性物种。基于中间体分析提出了TC的降解途径。此外,NZVI/g-CN@EGC在五轮测试中显示出高稳定性,并具有良好的磁性,便于从水溶液中分离。从应用角度来看,NZVI/g-CN@EGC在抗生素废水光催化降解方向上具有良好的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9082423/f7b3c82bf236/c9ra06620a-f1.jpg

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