氯苯
化学
降级(电信)
催化作用
介质阻挡放电
响应面法
反应机理
中心组合设计
臭氧
分析化学(期刊)
环境化学
色谱法
有机化学
物理化学
电极
电信
计算机科学
作者
Xin Yu,Xueping Dang,Shijie Li,Xiangkang Meng,Hao Hou,Pengyong Wang,Qi Wang
出处
期刊:Chemosphere
[Elsevier]
日期:2022-07-01
卷期号:298: 134274-134274
被引量:13
标识
DOI:10.1016/j.chemosphere.2022.134274
摘要
Dielectric barrier discharge coupled with 10 wt% Co/γ-Al2O3 catalyst was developed to degrade chlorobenzene in this study. The effects of experimental parameters including applied voltage, flow rate, initial chlorobenzene concentration, and their interactions on the chlorobenzene degradation performance were investigated by the response surface methodology integrated with a central composite design. Results indicated that applied voltage was the most significant parameter affecting the mineralization rate and the concentration of ozone generated, while energy yield was mainly determined by initial chlorobenzene concentration. As a key precursor of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorophenols were found during the identification of the intermediates produced during chlorobenzene degradation through GC-MS. Furthermore, HRGC-HRMS was used to detect the remaining byproducts on the catalyst surface after 3 and 10 h discharge time, and three types of PCDD/Fs (2,3,7,8-TCDF, 1,2,3,4,6,7,8-HCDF and OCDD) were detected after 10 h of discharge. The degradation mechanism of chlorobenzene was analyzed based on these detected intermediates, and the possible formation mechanisms of the three PCDD/Fs were proposed for the first time in plasma catalytic degradation of chlorobenzene.
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