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硫酸自由基在水处理中的反应特性 被引量:9

Response characteristics of sulfate radicals in water treatment
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摘要 从反应机理上解释了.OH和SO4.相似的原因,研究了硫酸自由基(SO4.)在水处理中的反应特性,探讨了其夺取有机物中C==C键、苯环上π电子和H能力的强弱.一般情况,SO4.的反应活性次序是:夺非芳香π电子>夺芳香π电子(苯系)>夺α-H>夺非α-H.SO4.降解有机物的效率除与有机物结构有关外,还与所处的介质环境有关,即与周围物质的碰撞几率相关,在水处理中由于SO4.与H2O分子反应的机会最多,一部分SO4.夺取H2O分子中H,生成羟自由基. In this paper,the reaction mechanism for similar products of hydroxyl radicals(.OH) and sulfate radicals(SO4.) were explained,the response properties of sulfate radicals in water treatment was investigated,and the ability of sulfate radicals to capture the π electron on C==C chemical bond,benzene ring and H atom in organic matters was discussed as well.Results show that capturing ability of sulfate radicals is generally ranked as the following:π electron in nonaromatic compounds π electron in aromatic compounds(benzene series) α-H non α-H in compound.The organic matter degradation efficiency of sulfate radicals is related to not only the structure of organic matter,but also to the medium environment,that is,it related to the collision probability of surrounding matter.Hydroxyl radicals are produced when sulfate radicals capture the hydrogen atom of H2O in aqueous reaction due to the most reaction opportunities between sulfate radicals and water molecules.
出处 《科学通报》 EI CAS CSCD 北大核心 2012年第36期3493-3499,共7页 Chinese Science Bulletin
基金 国家自然科学基金(51078047) 大连市科技计划(2010E14SF150) 中央高校基本科研业务经费资助
关键词 硫酸自由基 羟自由基 α-H Π电子 sulfate radical hydroxyl radical α-H π electron
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  • 1George C, Rassy H E, Chovelon J M, et al. Reactivity of selected volatile organic compounds toward the sulfate radical (SO4·-). Int J Chem Kinkt, 2001, 33: 539-547.
  • 2Padmaja S, Alfassi Z B, Neta P, et al. Rate constants for reaction of (SO4·-)radicals in acetonitrile. Int J Chem Kinkt, 1993, 25: 193-198.
  • 3Arciprete M L, Cobos C J, Fessenden R W. Reaction of sulphate reaction substituted pyridines: A structure-reactivity correlation analysis. Chemphyschem, 2007, 8: 2498-2505.
  • 4Neta P, Madhavan V, Zemel H. Rate constants and mechanism of reaction of SO4·-with aromatic compounds. J Am Chem Soc, 1977, 99: 163-164.
  • 5Muller J G, Hickerson R P, Perez R J. DNA damage from sulfite autoxidation catalyzed by a nickel(II) peptide. J Am Chem Soc, 1997, 119: 1501-1506.
  • 6张金凤,杨曦,郑伟,高颖.水体系中Fe(Ⅱ)/K2S2O8降解敌草隆的研究[J].环境化学,2008,27(1):15-18. 被引量:19
  • 7徐向荣,王文华,李华斌.比色法测定Fenton反应产生的羟自由基及其应用[J].生物化学与生物物理进展,1999,26(1):67-69. 被引量:89
  • 8魏鹏,沈帆,谢鹰.还原-偶氮光度法测定硝基苯的改进研究[J].湖北工业大学学报,2011,26(5):43-46. 被引量:5
  • 9史惠祥,徐献文,汪大翚.US/O_3降解对硝基苯酚的影响因素及机理[J].化工学报,2006,57(2):390-396. 被引量:36
  • 10Liang C J, Bruell C J, Marley M C, et al. Persulfate oxidation for in situremediation of TCE: I. Activated by ferrous ion with and without apersulfate2thiosulfate redox couple. Chemosphere, 2004, 55: 1213-1223.

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