期刊
JOURNAL OF HAZARDOUS MATERIALS
卷 329, 期 -, 页码 272-279出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhazmat.2017.01.046
关键词
Peroxides; Dyes; Photoexcitation; Electron transfer; Active radicals
资金
- Natural Science Foundation of Hubei Province [2012FFA089]
- Natural Science Foundation of China [21547006]
- Wuhan Applied Basic Research Project [2016060101010074]
- Shenzhen Basic Research Plan Project [JCYJ20150508152951667]
Catalysts are known to activate peroxides to generate active radicals (i.e., hydroxyl radical ((OH)-O-center dot) and sulfate radical (SO4 center dot-)) under certain conditions, but the activation of peroxides in the absence of catalysts under visible light irradiation has been rarely reported. This work demonstrates a catalyst-free activation of peroxides for the generation of (OH)-O-center dot and/or SO4 center dot- through photoexcited electron transfer from organic dyes to peroxides under visible LED light irradiation, where Rhodamine B (RhB) and Eosin Y (EY) were selected as model dyes. The formation of (OH)-O-center dot and/or SO4 center dot- in the reactions and the electron transfer from the excited dyes to peroxides were validated via electron paramagnetic resonance (EPR), photoluminescence (PL) spectra and cyclic voltammetry (CV). The performance of the peroxide/dye/Vis process was demonstrated to be altered depending on the target substrate. Meanwhile, the peroxide/dye/Vis process was effective for simultaneous decolorization of dyes and production of active radicals under neutral even or basic conditions. The findings of this study clarified a novel photoexcitation pathway for catalyst-free activation of peroxides under visible light irradiation, which could avoid the secondary metal ion (dissolved or leached) pollution from the metal-based catalysts and expand the application range of the peroxide-based catalytic process. (C) 2017 Elsevier B.V. All rights reserved.
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