Different non-radical oxidation processes of persulfate and peroxymonosulfate activation by nitrogen-doped mesoporous carbon

被引:75
作者
Qiu, Hai-Bin [1 ]
Guo, Pu-Can [1 ]
Yuan, Li [1 ]
Sheng, Guo-Ping [1 ]
机构
[1] Univ Sci & Technol China, Dept Appl Chem, CAS Key Lab Urban Pollutant Convers, Hefei 230026, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Nitrogen-doped mesoporous carbon; Persulfate; Peroxymonosulfate; Non-radical process; Electron transfer; Singlet oxygen formation; ORGANIC POLLUTANTS; WATER-TREATMENT; PHOTOSENSITIZED OXIDATION; DEGRADATION; NANOTUBES; SILICA;
D O I
10.1016/j.cclet.2020.08.014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Activated persulfate oxidation is an emerging advanced oxidation process for organic pollutant degradation. Own to different molecular structures and oxidation potentials, persulfate (PDS) and peroxymonosulfate (PMS) may show different degradation performances due to various catalytic mechanisms even by the same catalysts. In this study, the nitrogen-doped mesoporous carbon (N-OMC) was applied to activate PDS and PMS for degrading a model organic pollutant phenol to reveal their activation mechanisms. Results show that both PDS and PMS could be efficiently activated by N-OMC. The degradation of phenol fitted well with pseudo-first-order kinetics, whose kinetic constants increased with the increase of pH, PDS/PMS dosage, and N-OMC dosage. Based on quenching experiments and electron spin resonance spin-trapping technique, the N-OMC was found to activate PDS and PMS via non-radical process of electron transfer and singlet oxygen formation, respectively, instead of the commonly observed radical process. This work will be useful to understand the activation processes of PDS and PMS, and benefit for the development of catalysts for pollutant degradation. (C) 2020 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2614 / 2618
页数:5
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