详细信息

Comparison of naphthalene degradation by hydrogen peroxide, nano-calcium peroxide, peroxydisulfate, and peroxymonosulfate in the Fe(II)-citric acid catalytic environments  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Comparison of naphthalene degradation by hydrogen peroxide, nano-calcium peroxide, peroxydisulfate, and peroxymonosulfate in the Fe(II)-citric acid catalytic environments

作者:Zhang, Ruzhuang[1];Fang, Xingbin[1];Liu, Yulong[2];Li, Ming[1];Zeng, Guilu[2];Yang, Ruming[2];Qiu, Yiqin[1];Lyu, Shuguang[2]

机构:[1]Shanghai Chengtou Environm Ecol Remediat Technol C, Shanghai 200232, Peoples R China;[2]East China Univ Sci & Technol, State Environm Protect Key Lab Environm Risk Asses, Shanghai 200237, Peoples R China

年份:2024

卷号:24

期号:1

起止页码:71

外文期刊名:WATER SUPPLY

收录:;EI(收录号:20240815572314);WOS:【SCI-EXPANDED(收录号:WOS:001143739600001)】;

基金:This study was sponsored by the Shanghai Rising-Star Program (No. 22QB1401700) and the Shanghai State owned Assets Supervision and Administration Commission Enterprise Innovation Development and Energy Level Enhancement Project (No. CTKY-PTZX-2022-024).

语种:英文

外文关键词:activation; chemical oxidation; groundwater remediation; mechanism; reactive oxygen species

摘要:Naphthalene (NAP) was chosen as a target contaminant due to its increasing environmental concern in this work. Using hydrogen peroxide (H2O2), nano-calcium peroxide (nCP), peroxydisulfate (PDS), and peroxymonosulfate (PMS) as oxidants activated by Fe(II)-citric acid (CA) in aqueous solution, 92.8, 95.0, 97.5, and 99.9% of NAP were removed, respectively, in which CA could significantly enhance NAP degradation. HO center dot was demonstrated to be the major radical responsible for NAP removal in H2O2/Fe(II)/CA and nCP/Fe(II)/CA processes; both HO center dot and SO4 center dot- were major radicals in PDS/Fe(II)/CA process, whereas SO4 center dot- was the sole dominant radical in PMS/Fe(II)/CA process. The impacts of water matrices (anions, natural organic matters, and surfactants) and initial solution pH on NAP removal as well as the practicalities of these four systems in groundwater were explored. The efficient NAP degradation of nCP/Fe(II)/CA and PMS/Fe(II)/CA processes in the actual groundwater indicated that these two systems have great potential and advantages in the remediation of NAP-contaminated groundwater.

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