Transformation of dissolved organic matter during UV/peracetic acid treatment

被引:19
|
作者
Du, Penghui [1 ,2 ]
Liu, Wen [3 ]
Zhang, Qiang [1 ,2 ]
Zhang, Peng [1 ,2 ]
He, Chen [4 ]
Shi, Quan [4 ]
Huang, Ching-Hua [5 ]
Wang, Junjian [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Sch Environm Sci & Engn, Guangdong Key Lab Soil & Groundwater Pollut Contro, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Sch Environm Sci & Engn, State Environm Protect Key Lab Integrated Surface, Shenzhen 518055, Guangdong, Peoples R China
[3] Peking Univ, Coll Environm Sci & Engn, Key Lab Water & Sediment Sci, Minist Educ, Beijing 100871, Peoples R China
[4] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[5] Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
关键词
Peracetic acid; Dissolved organic matter; ESI FT-ICR MS; Advanced oxidation process; Wastewater treatment; DISINFECTION BY-PRODUCT; PERACETIC-ACID; HYDROXYL RADICALS; CARBON AOC; OXIDATION; DEGRADATION; OZONATION; KINETICS; CHLORINE; INDEX;
D O I
10.1016/j.watres.2023.119676
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Peracetic acid combined ultraviolet (UV/PAA) process has garnered growing attention as a promising advanced oxidation process (AOP) for wastewater treatment, but the corresponding transformation of ubiquitous dissolved organic matter (DOM) under this AOP remains unknown. This study systematically investigated the changes in characteristics and composition of DOM under UV/PAA, as well as the underlying mechanisms by multiple spectroscopic analyses and Fourier transform ion cyclotron resonance mass spectrometry. UV/PAA treatment dramatically decreased aromaticity, apparent molecular weight, and fluorescent abundance of DOM with the production of more oxidized and saturated compounds. The reactive species (i.e., .OH and CH3C(O)O./CH3C(O)OO.) in UV/PAA contributed primarily to DOM changes but showed different reaction selectivity and mecha-nisms. .OH reacts with DOM components and mainly yields oxygenation products via a radical addition pathway. Comparatively, the electron transfer route is more likely to occur in CH3C(O)O./CH3C(O)OO.-induced DOM transformation. Aside from oxygenation products, electron transfer could exclusively generate decarboxylation products and distinguishes CH3C(O)O./CH3C(O)OO.-based AOPs from .OH-based AOPs. These findings signifi-cantly improve knowledge of DOM alterations under UV/PAA AOP at both the bulk and molecular levels.
引用
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页数:9
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