Optimization of the catalytic activity of a ZnCo2O4 catalyst in peroxymonosulfate activation for bisphenol A removal using response surface methodology

被引:59
|
作者
Hu, Limin [1 ]
Zhang, Guangshan [1 ]
Liu, Meng [1 ]
Wang, Qiao [1 ]
Wang, Peng [1 ]
机构
[1] Harbin Inst Technol, Sch Environm, State Key Lab Urban Water Resource & Environm, Harbin 150090, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
ZnCo2O4; Peroxymonosulfate; Bisphenol A; Response surface methodology; Radical species; REDUCED GRAPHENE OXIDE; ENHANCED HETEROGENEOUS ACTIVATION; MICROWAVE-ASSISTED METHOD; AQUEOUS-SOLUTION; ORGANIC POLLUTANTS; FACILE SYNTHESIS; EFFICIENT DEGRADATION; ADSORPTIVE REMOVAL; CARBON NANOTUBES; MAGNETIC COFE2O4;
D O I
10.1016/j.chemosphere.2018.08.065
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
An effective peroxymonosulfate activator, ZnCo2O4, was synthesized through a microwave-assisted method. According to response surface methodology (RSM) using Box-Behnken design (BBD), the effects of four parameters, microwave temperature, microwave time, calcination time and calcination temperature, were investigated, and the results show that both the microwave temperature and calcination temperature have a great influence on the catalytic activity during the preparation process. In addition, a quadratic model is valid for computing and predicting the observed responses. The characteristics of the synthesized ZnCo2O4 catalyst were analyzed with various equipments. The results show that the ZnCo2O4 nanosheets are cubic crystals with a spinel structure and a high surface area of 105.90 m(2).g(-1). Under the conditions of [ZnCo2O4]= 0.2 g.L-1 and [PMS]/[BPA](molar) = 2.0, the bisphenol A degradation efficiency reaches 99.28% within 5 min in the ZnCo2O4/PMS system. ZnCo2O4 possesses great stability and reusability according to recycling experiments. In addition, the possible active radical species were confirmed through quenching experiments and EPR detection, indicating that surface bound SO4 center dot- and center dot OH play vital roles during the degradation process. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:152 / 161
页数:10
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