过氧化氢
光催化
催化作用
化学
原位
激进的
分解
降级(电信)
光化学
化学工程
有机化学
电信
计算机科学
工程类
作者
Pengfei Jin,Zhiguo Cao,Bin He
出处
期刊:Chemosphere
[Elsevier BV]
日期:2023-04-30
卷期号:332: 138820-138820
被引量:9
标识
DOI:10.1016/j.chemosphere.2023.138820
摘要
Although many concerns have been put into photocatalytic hydrogen peroxide (H2O2) production, multifunctional catalysis suitable for continuously in-situ H2O2 consumption in the field has rarely been investigated. Herein, Cu0@CuOx@nitrogen-doped graphitic carbon (Cu0@CuOx-NC) decorated Zn2In2S5 was successfully prepared for in-situ production and activation H2O2, which could achieve effectively photocatalytic self-Fenton degradation of tetracycline (TC). Under visible light irradiation, 5 wt% Cu0@CuOx-NC/Zn2In2S5 (CuZS-5) efficiently generated a high yield of H2O2 (0.13 mmol L-1), and Cu0@CuOx-NC could in-situ consume H2O2 to generate hydroxyl radicals (•OH), accelerating the oxidation of TC. As a result, the 5 wt% Cu0@CuOx-NC/Zn2In2S5 degraded about 89.3% of TC within 60 min, and the cycle experiments also exhibited sufficient stability. This study achieves a delicate combination of in-situ production and activation of H2O2, which is regarded as a promising strategy to eco-friendly promote pollutant degradation in wastewater.
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