过硫酸盐
化学
介孔材料
催化作用
单线态氧
降级(电信)
猝灭(荧光)
苯酚
电子顺磁共振
电子转移
动力学
激进的
无机化学
光化学
氧气
荧光
有机化学
电信
物理
核磁共振
量子力学
计算机科学
作者
Hai-Bin Qiu,Pu-Can Guo,Yuan Li,Guo‐Ping Sheng
标识
DOI:10.1016/j.cclet.2020.08.014
摘要
Abstract 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.
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