Qin Hangdao, Hao Junnan, Wang Yong, Huang Jiming, Chang Jun, Yang Guo, Xing Bo, Wu Sizhan, Chen Jing
School of Material and Chemical Engineering, Tongren University Tongren 554300 China
College of Chemical Engineering, Sichuan University of Science and Engineering Zigong 643000 China.
RSC Adv. 2025 Apr 8;15(14):11045-11055. doi: 10.1039/d5ra01539a. eCollection 2025 Apr 4.
Electrolytic manganese residue (EMR) was used as a support to prepare novel EMR-supported catalysts for the heterogeneous Fenton degradation of acetaminophen. Among the five supported catalysts, Co/EMR showed the highest catalytic activity. Several important factors influencing the decay of acetaminophen, including Co loading content, catalyst dosage, HO concentration and initial solution pH, were investigated. Under optimal experimental conditions, acetaminophen degradation rate and the TOC removal efficiency reached 63.8% and 35.7% within 480 min, respectively. Free radical quenching and EPR analysis showed that the high catalytic degradation rate of acetaminophen could be ascribed to the presence of ˙OH and O˙. Based on the XPS analysis, the superior catalytic performance of Co/EMR was attributed to the Fe, Mn and Co active sites and oxygen vacancies (O) on the surface. Additionally, the potential for degradation of other pollutants and the applicability in real water matrices as well as the reusability of Co/EMR were investigated. This heterogeneous Fenton system could expand possibilities for high-value utilization of the EMR and showed potential for treating PPCPs in wastewater.
以电解锰渣(EMR)为载体,制备了用于对乙酰氨基酚非均相芬顿降解的新型EMR负载型催化剂。在五种负载型催化剂中,Co/EMR表现出最高的催化活性。研究了影响对乙酰氨基酚降解的几个重要因素,包括钴负载量、催化剂用量、羟基自由基(·OH)浓度和初始溶液pH值。在最佳实验条件下,对乙酰氨基酚在480分钟内的降解率和总有机碳(TOC)去除效率分别达到63.8%和35.7%。自由基淬灭和电子顺磁共振(EPR)分析表明,对乙酰氨基酚的高催化降解率可归因于·OH和超氧自由基(O2·-)的存在。基于X射线光电子能谱(XPS)分析,Co/EMR的优异催化性能归因于其表面的铁、锰和钴活性位点以及氧空位(Ov)。此外,还研究了Co/EMR对其他污染物的降解潜力、在实际水体基质中的适用性以及可重复使用性。这种非均相芬顿体系为电解锰渣的高值化利用拓展了可能性,并显示出处理废水中新兴有机污染物(PPCPs)的潜力。