UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors

Ultraviolet-activated permanganate (UV/PM) process is a novel advanced oxidation process (AOP), but its application potential remains to be evaluated. This work investigates the degradation of refractory organic pollutant by UV/PM in terms of efficiency, mechanism, and influencing factors. The targe...

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Autores principales: Miaomiao Ye, Chengzhuo Li, Xiaowei Liu, Lili Wang, Rong Chen
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Lenguaje:EN
Publicado: IWA Publishing 2021
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Acceso en línea:https://doaj.org/article/5e67250f4bf049e6adb63b3ee91998ac
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spelling oai:doaj.org-article:5e67250f4bf049e6adb63b3ee91998ac2021-11-06T10:52:17ZUV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors0273-12231996-973210.2166/wst.2021.068https://doaj.org/article/5e67250f4bf049e6adb63b3ee91998ac2021-03-01T00:00:00Zhttp://wst.iwaponline.com/content/83/6/1278https://doaj.org/toc/0273-1223https://doaj.org/toc/1996-9732Ultraviolet-activated permanganate (UV/PM) process is a novel advanced oxidation process (AOP), but its application potential remains to be evaluated. This work investigates the degradation of refractory organic pollutant by UV/PM in terms of efficiency, mechanism, and influencing factors. The target compound benzoic acid (BA), which is a micro-organic pollutant and is resistant to PM and UV treatment, can be efficiently degraded by UV/PM. The electron paramagnetic resonance spectra directly supported the formation of hydroxyl radical (HO•) and superoxide radical from UV photolysis of PM. Competitive kinetics experiments verified that acted as precursor of HO• and the good degradation performance of BA was due to the involvement of HO• and manganese(V). The rate constants of BA degradation showed a positive linear relationship with PM dosage in the range of 0.5–20 mg·L−1, and the degradation process was significantly influenced by solution pH and natural organic matters but insensitive to chloride and bicarbonate at environmentally relevant concentrations. Compared to the typical UV-based AOP UV/hydrogen peroxide, UV/PM is a little inferior, indicating that optimization and enhancement is needed for this process before its possible practical application. HIGHLIGHTS The mechanism of HO• generation from photolysis of PM was parsed.; The effects of operating parameters (e.g. PM dosage, pH, natural organic matters, alkalinity, and chloride) on UV/PM process were investigated.; UV/PM process was compared with UV/H2O2.; Optimization and enhancement is needed for UV/PM process before its possible practical application.;Miaomiao YeChengzhuo LiXiaowei LiuLili WangRong ChenIWA Publishingarticleactive manganese specieshydroxyl radicalpermanganateuv activationEnvironmental technology. Sanitary engineeringTD1-1066ENWater Science and Technology, Vol 83, Iss 6, Pp 1278-1285 (2021)
institution DOAJ
collection DOAJ
language EN
topic active manganese species
hydroxyl radical
permanganate
uv activation
Environmental technology. Sanitary engineering
TD1-1066
spellingShingle active manganese species
hydroxyl radical
permanganate
uv activation
Environmental technology. Sanitary engineering
TD1-1066
Miaomiao Ye
Chengzhuo Li
Xiaowei Liu
Lili Wang
Rong Chen
UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
description Ultraviolet-activated permanganate (UV/PM) process is a novel advanced oxidation process (AOP), but its application potential remains to be evaluated. This work investigates the degradation of refractory organic pollutant by UV/PM in terms of efficiency, mechanism, and influencing factors. The target compound benzoic acid (BA), which is a micro-organic pollutant and is resistant to PM and UV treatment, can be efficiently degraded by UV/PM. The electron paramagnetic resonance spectra directly supported the formation of hydroxyl radical (HO•) and superoxide radical from UV photolysis of PM. Competitive kinetics experiments verified that acted as precursor of HO• and the good degradation performance of BA was due to the involvement of HO• and manganese(V). The rate constants of BA degradation showed a positive linear relationship with PM dosage in the range of 0.5–20 mg·L−1, and the degradation process was significantly influenced by solution pH and natural organic matters but insensitive to chloride and bicarbonate at environmentally relevant concentrations. Compared to the typical UV-based AOP UV/hydrogen peroxide, UV/PM is a little inferior, indicating that optimization and enhancement is needed for this process before its possible practical application. HIGHLIGHTS The mechanism of HO• generation from photolysis of PM was parsed.; The effects of operating parameters (e.g. PM dosage, pH, natural organic matters, alkalinity, and chloride) on UV/PM process were investigated.; UV/PM process was compared with UV/H2O2.; Optimization and enhancement is needed for UV/PM process before its possible practical application.;
format article
author Miaomiao Ye
Chengzhuo Li
Xiaowei Liu
Lili Wang
Rong Chen
author_facet Miaomiao Ye
Chengzhuo Li
Xiaowei Liu
Lili Wang
Rong Chen
author_sort Miaomiao Ye
title UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
title_short UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
title_full UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
title_fullStr UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
title_full_unstemmed UV-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
title_sort uv-activated permanganate process for micro-organic pollutant degradation: efficiency, mechanism and influencing factors
publisher IWA Publishing
publishDate 2021
url https://doaj.org/article/5e67250f4bf049e6adb63b3ee91998ac
work_keys_str_mv AT miaomiaoye uvactivatedpermanganateprocessformicroorganicpollutantdegradationefficiencymechanismandinfluencingfactors
AT chengzhuoli uvactivatedpermanganateprocessformicroorganicpollutantdegradationefficiencymechanismandinfluencingfactors
AT xiaoweiliu uvactivatedpermanganateprocessformicroorganicpollutantdegradationefficiencymechanismandinfluencingfactors
AT liliwang uvactivatedpermanganateprocessformicroorganicpollutantdegradationefficiencymechanismandinfluencingfactors
AT rongchen uvactivatedpermanganateprocessformicroorganicpollutantdegradationefficiencymechanismandinfluencingfactors
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