On the increasing competitiveness of UV/Cl to UV/H2O2 advanced oxidation as the organic carbon concentration increases

被引:9
作者
Moore, Nathan [1 ]
Wang, Chengjin [1 ,2 ]
Andrews, Susan [1 ]
Hofmann, Ron [1 ]
机构
[1] Univ Toronto, Dept Civil & Mineral Engn, 35 St George St, Toronto, ON M5S 1A4, Canada
[2] Univ Manitoba, Dept Civil Engn, 15 Gillson St, Winnipeg, MB R3T 5V6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
UV -based advanced oxidation; UV; chlorine; hydrogen peroxide; Scavenging; Organic matter; HYDROXYL RADICALS; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTIONS; DEGRADATION; PHOTOLYSIS; ROLES; IONS;
D O I
10.1016/j.watres.2023.120227
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
UV/Cl and UV/H2O2 are advanced oxidation processes (AOPs) used for drinking water treatment and water reuse. This work explored the hypothesis that UV/Cl becomes more competitive to UV/H2O2 at neutral-to-high pH as the concentration of total organic carbon (TOC) increases. Lab experiments and kinetic modelling were used to compare initial pseudo first-order contaminant decay rate coefficients between the AOPs at various pH and TOC conditions. The relative effect of increasing TOC concentrations on UV/Cl vs. UV/H2O2 depended on the pH, contaminant, and organic matter reactivity towards radicals. For example, while the reaction rate coefficients during both AOPs generally decreased with increasing TOC, the UV/Cl reaction rate coefficients for the solely & BULL;OH-reactive sucralose decreased 41-138% less than the UV/H2O2 coefficients as the TOC concentration was increased from 0 to 5 mg-C L-1. However, UV/Cl was more affected than UV/H2O2 when targeting caffeine (a contaminant reactive to chlorine radicals). The data were used to define TOC-pH conditions for which either AOP would be more energy-efficient, under a set of standard conditions. The results suggest that UV/Cl may be competitive to UV/H2O2 under a wider range of treatment scenarios than has been conventionally thought based on tests in pure water.
引用
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页数:8
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