过硫酸盐
双金属片
降级(电信)
催化作用
化学
动力学
光化学
核化学
化学工程
有机化学
电信
计算机科学
工程类
物理
量子力学
作者
Tianning Wang,Xiuming Liu,Jixian Gong,Jinkun Wang,Enzheng Xing,Jiayu Wang,Hongpei Zhang
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-05-14
卷期号:40 (21): 11039-11048
被引量:6
标识
DOI:10.1021/acs.langmuir.4c00485
摘要
The synergistic effect between bimetallic catalysts has been confirmed as an effective method for activating persulfate (PMS). Therefore, we immobilized copper–cobalt on chitosan to prepare bimetallic carbon catalysts for PMS activation and degradation of reactive dyes. Experimental results demonstrate that the CuCo-CTs/PMS catalytic degradation system exhibits excellent degradation performance toward various types of reactive dyes (e.g., Ethyl violet, Chlortalidone, and Di chlorotriazine), with degradation rates reaching 90% within 30 min. CuCo-CTs exhibit high catalytic activity over a wide pH range of 3–11 at room temperature and under static conditions, degrading over 92% of RV5 within 60 min. ultraviolet–visible (UV–vis) spectroscopy and color changes in the dye solution confirm the effective degradation of RV5, with a degradation rate of 97.2% within 10 min. Additionally, CuCo-CTs demonstrate good stability and reusability, maintaining a degradation rate of 92.8% after eight cycles. Kinetic studies indicate that the degradation follows pseudo-first-order kinetics. Furthermore, based on the results of radical scavenging experiments, the catalytic degradation mechanism of the dye involves both radical and nonradical pathways, with 1O2 identified as the primary active species. This study provides insights and experimental evidence for the application of persulfate oxidation in the treatment of dyeing wastewater.
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