催化作用
化学
氧气
煅烧
降级(电信)
氧化还原
羟基自由基
矿化(土壤科学)
无机化学
环境化学
核化学
激进的
有机化学
电信
计算机科学
氮气
作者
Yingying Gu,Zuzhao Wu,Yuanyuan Shen,Chen Lǚ,Liuli Lu,Zengxin Bian,Xiu-Xia Zhang,Chaocheng Zhao,Rongbing Fu,Hongjiang Li
出处
期刊:Chemosphere
[Elsevier]
日期:2023-07-21
卷期号:338: 139540-139540
被引量:9
标识
DOI:10.1016/j.chemosphere.2023.139540
摘要
In the Fenton-like processes, the resources that exist in the system itself (e.g., dissolved oxygen, electron-rich pollutants) are often overlooked. Herein, a novel CuCo-LDO/CN composite catalyst with a strong "metal-π" effect was fabricated by in situ calcination which could activate dissolved oxygen to generate active oxygen species and degrade the electron-rich pollutants directly. The CuCo-LDO/CN (1:10) with the largest specific surface aera, most C-O-M bonds and least oxygen vacancies exhibited the best catalytic performance for tetracycline (TC)degradation (TC removal efficiency 93.2% and mineralization efficiency 40%, respectively, after 40 min at neutral pH) compared to CuCo-LDO and other CuCo-LDO/CN composite catalysts. In the absence of H2O2, dissolved oxygen could be activated by the catalyst to generate O2·-and ·OH, which contributed to approximately 20.7% of TC degradation, providing a faster and cost-effective way for TC removal from wastewater. While in the presence of H2O2, it was activated by CuCo-LDO/CN to generate·OH as the dominant reactive oxygen species and meanwhile TC transferred electrons to H2O2 through C-O-M bonds, accelerating the Cu+/Cu2+ and Co2+/Co3+ redox cycles. The possible degradation pathways of TC were proposed, and the environmental hazard of TC is greatly mitigated according to toxicity prediction.
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