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首页|期刊导航|环境工程学报|双金属阳极膜电催化原位产臭氧去除废水中的盐酸四环素

双金属阳极膜电催化原位产臭氧去除废水中的盐酸四环素

程心悦 张晓楠 高兆鹤 何亮 关清卿 周华晶

环境工程学报2025,Vol.19Issue(3):595-604,10.
环境工程学报2025,Vol.19Issue(3):595-604,10.DOI:10.12030/j.cjee.202409108

双金属阳极膜电催化原位产臭氧去除废水中的盐酸四环素

Removal of tetracycline from wastewater by in situ-produced ozone through bimetallic anode membrane electrocatalysis

程心悦 1张晓楠 2高兆鹤 1何亮 2关清卿 1周华晶1

作者信息

  • 1. 昆明理工大学建筑工程学院,昆明 650500
  • 2. 昆明理工大学化学工程学院,昆明 650500
  • 折叠

摘要

Abstract

In this study,the electrospinning technology was used to synthesize the CoMo-electrocatalytic anode membrane(CoMo-ECM)for the degradation of tetracycline(TC-HCl).The results showed that the degradation of TC-HCl followed a quasi-first-order kinetic,with a degradation rate constant and half-life of 0.24 min-1 and 2.9 min,respectively,at a current density of 10 mA·cm2.The highest degradation rate occurred under neutral partial acid conditions(pH=5~6),and the removal rate approached to 100%at 40 min.During electrochemical degradation,five intermediate products were identified.The main degradation pathways relied on reactive oxygen species(ROS)derived from the cracking of ozone with high concentrations,which was produced in situ by anodic catalytic membranes,mainly including three types of ROSs:·OH,1O2 and·O2-.The double-bonded carbon atom near the hydroxymethyl group is the location where·OH attacked,and the cleavage of the Co-N bond is the rate-limiting step of the electrochemical degradation of the TC-HCl.The nitrogen in TC-HCl mainly converted to nitrate and ammonium.The results showed that CoMo-ECM,as an anode membrane,can in-situ produce ozone and efficiently degrade TC-HCl.

关键词

静电纺丝/形貌控制/电催化/盐酸四环素/臭氧

Key words

electrospinning/morphology control/electrocatalysis/tetracycline hydrochloride/ozone

分类

环境科学

引用本文复制引用

程心悦,张晓楠,高兆鹤,何亮,关清卿,周华晶..双金属阳极膜电催化原位产臭氧去除废水中的盐酸四环素[J].环境工程学报,2025,19(3):595-604,10.

基金项目

国家自然科学基金重点资助项目(52260009) (52260009)

云南省科技厅科技计划项目(202303AG100002-03) (202303AG100002-03)

环境工程学报

OA北大核心

1673-9108

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