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Fe^(2+)/PMS同步处理锰和有机物复合污染原水 被引量:2

Add to Favorite Get Latest Update Fe~(2+)/PMS System for Simultaneous Removal of Manganese and Organic Matter from Combined Polluted Raw Water
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摘要 针对复合污染原水中锰和天然有机物的同步去除问题,研究了亚铁/过氧单硫酸盐(Fe^(2+)/PMS)体系的去除途径和效果。结果表明:在复合污染条件下,当原水中Mn^(2+)由0增加至1.0mg/L时,Fe^(2+)/PMS体系对DOC和UV254的去除率分别提高了7.39%和3.58%,而出水锰浓度为0.01~0.79μg/L,表明Fe^(2+)/PMS体系可以同步去除复合污染原水中的锰和天然有机物。机理分析表明,Mn2+的存在促进了Fe^(2+)/Fe^(3+)循环,强化自由基产生的同时促进了Fe^(3+)的生成,且其氧化产物Mn O_(2)具有较好的助凝作用。动力学分析表明,Mn2+对Fe^(2+)/PMS体系的强化作用主要在慢速反应阶段,提高了对有机物的去除效果。 To achieve simultaneous removal of manganese and natural organic matter from combined polluted raw water,the removal pathway and performance of ferrous/peroxymonosulfate(Fe^(2+)/PMS)system were investigated.When the Mn^(2+)concentration in combined polluted raw water increased from 0 to 1.0 mg/L,the removal rates of DOC and UV_(254)in the Fe^(2+)/PMS system increased by 7.39%and3.58%,respectively,and the manganese concentration in effluent ranged from 0.01μg/L to 0.79μg/L,indicating that the system could be used for simultaneous removal of manganese and natural organic matter from combined polluted raw water.The mechanism analysis showed that the presence of Mn^(2+)promoted the Fe^(2+)/Fe^(3+)cycle,enhanced the formation of free radicals and promoted the formation of Fe^(3+),and its oxidation product Mn O_2 had a good coagulation performance.The kinetic analysis showed that Mn^(2+)enhanced the coagulation of Fe^(2+)/PMS system mainly at the slow reaction stage,thus improved the removal efficiency of organic matter.
作者 陶辉 顾颖 林涛 蒋福春 张雪 TAO Hui;GU Ying;LIN Tao;JIANG Fu-chun;ZHANG Xue(Key Laboratory of Integrated Regulation and Resource Development on Shallow Lakers<Ministry of Education>,Hohai University,Nanjing 210098,China;College of Environment,Hohai University,Nanjing 210098,China;Nanjing Water Group,Nanjing 210002,China;Suzhou Water Supply Co.Ltd.,Suzhou 215124,China)
出处 《中国给水排水》 CAS CSCD 北大核心 2023年第15期64-69,共6页 China Water & Wastewater
基金 国家重点研发计划项目(2022YFC3203702)。
关键词 亚铁 过氧单硫酸盐 复合污染 天然有机物 同步去除 ferrous peroxymonosulfate combined pollution manganese natural organic matter simultaneous removal
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  • 1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
  • 2George 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.
  • 3Padmaja 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.
  • 4Arciprete M L, Cobos C J, Fessenden R W. Reaction of sulphate reaction substituted pyridines: A structure-reactivity correlation analysis. Chemphyschem, 2007, 8: 2498-2505.
  • 5Neta P, Madhavan V, Zemel H. Rate constants and mechanism of reaction of SO4·-with aromatic compounds. J Am Chem Soc, 1977, 99: 163-164.
  • 6Muller 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.
  • 7Liang 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.
  • 8Ali S A, James R. Bolton S R. Cater Ferrioxalate-mediated photodegradation of organic pollutants in contaminated. Water Res, 1997, 31: 787-798.
  • 9Anipsitakis G P, Dionysiou D D. Degradation of organic contaminants in water with sulfate radicals generated by the conjunction of peroxymonosulfate with cobalt. Environ Sci Technol, 2003, 37: 4790-4797.
  • 10Charuvila T A, Man N S, Balijepalli S M. Justus von Sonntag and Clemens von Sonntag. The reactions of cytidine and 2-deoxycytidine with (SO4·-)revisited. Pulse radiolysis and product studies. Org Biomol Chem, 2003, 1: 401-408.

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