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Fe2+/NH2OH联合活化过硫酸盐降解水中磺胺甲恶唑

李峰 刘桂芳 梁涛 王春丽 张玉平 蔡丽丽

高校化学工程学报2017,Vol.31Issue(5):1210-1216,7.
高校化学工程学报2017,Vol.31Issue(5):1210-1216,7.DOI:10.3969/j.issn.1003-9015.2017.00.037

Fe2+/NH2OH联合活化过硫酸盐降解水中磺胺甲恶唑

Degradation of Sulfamethoxazole in Aqueous Solution by Ferrous/Hydroxylamine Activated Peroxymonosulfate

李峰 1刘桂芳 1梁涛 2王春丽 1张玉平 1蔡丽丽1

作者信息

  • 1. 哈尔滨工程大学 航天与建筑工程学院,黑龙江 哈尔滨 150001
  • 2. 黑龙江工程学院 土木与建筑工程学院,黑龙江 哈尔滨 150050
  • 折叠

摘要

Abstract

Fe2+ activated peroxymonosulfate (Fe2+/PMS) as a Fenton-like oxidation system can produce strong reactive species and degrade many refractory organic contaminants in aqueous solutions. However, slow conversion of Fe3+ to Fe2+ dramatically limits extensive application of Fe2+/PMS systems. In this study, hydroxylamine (NH2OH) was used to strengthen the system to degrade a typical antibiotic. The degradation of sulfamethoxazole (SMX) was systematically investigated in Fe2+/NH2OH/PMS. The results indicate that dosage increase of PMS, Fe2+ and NH2OH can effectively promote SMX oxidation. In addition, solution temperature increase can promote reactive radical release and thus strengthen SMX degradation. However, the increase of SMX concentration and pH significantly inhibits SMX degradation. Furthermore, the analysis of reactive radicals shows that sulfate radical (SO?-4 ) is the primary active radical for the degradation of SMX in Fe2+/NH2OH/PMS.

关键词

过一硫酸盐/羟胺/磺胺甲恶唑/硫酸根自由基

Key words

peroxymonosulfate/hydroxylamine/sulfamethoxazole/sulfate radical

分类

资源环境

引用本文复制引用

李峰,刘桂芳,梁涛,王春丽,张玉平,蔡丽丽..Fe2+/NH2OH联合活化过硫酸盐降解水中磺胺甲恶唑[J].高校化学工程学报,2017,31(5):1210-1216,7.

基金项目

黑龙江省博士后资助 (LBH-Z13062) (LBH-Z13062)

哈尔滨市科技局项目(2014RFQXJ187). (2014RFQXJ187)

高校化学工程学报

OA北大核心CSCDCSTPCD

1003-9015

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