Efficient sulfamethoxazole degradation via boosting nonradical-based peroxymonosulfate activation by biochar supported Co-Ni bimetal oxide

被引:0
|
作者
Yu, Yueling [1 ,2 ,4 ]
Yang, Jia [2 ]
Zhao, Baogang [1 ]
Fan, Xinfei [2 ]
Xu, Yuanlu [3 ]
Liu, Yanming [4 ]
机构
[1] Dalian Maritime Univ, Marine Engn Coll, Dalian 116026, Peoples R China
[2] Dalian Maritime Univ, Coll Environm Sci & Engn, 1 Linghai Rd, Dalian 116026, Peoples R China
[3] Dalian Maritime Univ, Ctr Ports & Maritime Safety, Dalian 116026, Peoples R China
[4] Dalian Univ Technol, Sch Environm Sci & Technol, Key Lab Ind Ecol & Environm Engn, Minist Educ China, Dalian 116024, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Wastewater treatment; Advanced oxidation process; Peroxymonosulfate activation; Antibiotics; BISPHENOL-A; CATALYTIC-OXIDATION; CARBON NANOTUBES; PERFORMANCE; KINETICS; CIPROFLOXACIN; MECHANISMS; PATHWAYS;
D O I
10.1016/j.jece.2023.110903
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nonradical-based peroxymonosulfate (PMS) activation has recently caught increasing attention due to its less susceptible to environmental interference in the complex water matrix, but the performance of activators still requires further development for efficient pollutants degradation in wastewater treatment. Herein, a novel Co-Ni bimetal oxide loaded biochar was fabricated to boost nonradical PMS activation for enhancing sulfamethoxazole (SMX) degradation. According to the results, the as-obtained catalyst exhibited excellent SMX degradation efficiency of 96.2% within 30 min through complete nonradical oxidation pathway (including both 1O2 and mediated electron transfer). Co was confirmed to be the active sites to generate 1O2 dominated nonradical pathway. The biochar acted as the porous material to achieve the electron transfer oxidation process, as well as Ni ensured sufficient electron transfer rate and bound Co active sites to prevent the leaching of metal ions. Meanwhile, the prepared Co-Ni bimetal oxide loaded biochar possessed a remarkable catalytic degradation durability in the complex water environment conditions and showed universality for various organic contaminants. This study offers a valuable clue on the rational design of novel catalyst to induce the nonradical pathwaybased persulfate activation.
引用
收藏
页数:11
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