黄铁矿催化H2O2氧化降解水中三氯生

冯勇, 吴德礼, 马鲁铭. 黄铁矿催化H2O2氧化降解水中三氯生[J]. 环境工程学报, 2012, 6(10): 3433-3437.
引用本文: 冯勇, 吴德礼, 马鲁铭. 黄铁矿催化H2O2氧化降解水中三氯生[J]. 环境工程学报, 2012, 6(10): 3433-3437.
Feng Yong, Wu Deli, Ma Luming. Catalytic oxidation of triclosan in water by pyrite and hydrogen peroxide[J]. Chinese Journal of Environmental Engineering, 2012, 6(10): 3433-3437.
Citation: Feng Yong, Wu Deli, Ma Luming. Catalytic oxidation of triclosan in water by pyrite and hydrogen peroxide[J]. Chinese Journal of Environmental Engineering, 2012, 6(10): 3433-3437.

黄铁矿催化H2O2氧化降解水中三氯生

  • 基金项目:

    国家自然科学基金资助项目(50808136)

    上海科委长三角联合攻关项目(10195811400)

  • 中图分类号: X703

Catalytic oxidation of triclosan in water by pyrite and hydrogen peroxide

  • Fund Project:
  • 摘要: 以三氯生为目标污染物,研究了黄铁矿催化H2O2非均相类Fenton体系对污染物的去除效果,并利用SEM、EDS等手段对天然黄铁矿进行了表征。考察了催化剂、H2O2投加量、溶液初始pH、反应时间等重要因素对催化氧化反应的影响。在H2O2投加量5 mg/L,黄铁矿用量0.1 g/L,溶液初始pH为8,反应10 min后,三氯生的去除率达90%以上。相对于传统Fenton反应,pH对本非均相催化反应的影响较小,在2~10的pH范围内,仍有较高的催化活性。利用GC-MS分析显示,三氯生降解过程能够产生包括2,4-二氯苯酚在内的多种中间产物。
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  • [1] 贾瑷,胡建英,孙建仙,等.环境中的医药品与个人护理品.化学进展,2009,21(Z1):389-399 Jia Ai,Hu Jianying,Sun Jianxian,et al.Pharmaceuticals and personal care products (PPCPs) in environment.Progress in Chemistry,2009,21(Z1):389-399(in Chinese)
    [2] Jin J.,Su Y.P.Oxidation of triclosan by permanganate(MN(VII)):Importance of ligands and in situ formed manganese oxides.Environmental Science and Technology,2009,43(21):8326-8331
    [3] Orvis D.R.,Versteeg D.J.,Inurn J.,et al.Aquatic toxicity of triclosan.Environmental Toxicology and Chemistry,2002,21(7):1338-1349
    [4] Latch D.E.,Pacher J.L.,Stender B.L.,et al.Aqueous photochemistry of triclosan:Formation of 2,4-dichlorophenol,2,8-dichlorodibenzo-p-dioxin,and oligomerization products.Environmental Toxicology and Chemistry,2005,24(3):517-525
    [5] Sires I.,Oturan N.,Oturan M.A.,et al.Electro-Fenton degradation of antimicrobials triclosan and triclocarban.Electrochimica Acta,2007,52(17):5493-5503
    [6] Suarez S.,Dodd M.C.,Omil F.,et al.Kinetics of triclosan oxidation by aqueous ozone and consequent loss of antibacterial activity:Relevance to municipal wastewater ozonation.Water Research,2007,41(12):2481-2490
    [7] Zhang H.H.,Huang C.H.Oxidative transformation of triclosan and chlorophene by manganese oxides.Environment Science and Technology,2003,37(11):2421-2430
    [8] Bin Y.,Guang G.Y.,Jian L.Z.,et al.Oxidation of triclosan by ferrate:Reaction kinetics,products identification and toxicity evaluation.Journal of Hazardous Materials,2011,186(1):227-235
    [9] Liyanapatirana C.,Gwaltney S.,Xia K.Transformation of triclosan by Fe(III)-saturated montmorillonite.Environment Science and Technology,2010,44(2):668-674
    [10] Pham A.L.,Lee C.,Doyle F.M.,et al.A silica-supported iron oxide catalyst capable of activating hydrogen peroxide at neutral pH values.Environment Science and Technology,2009,43(23):8930-8935
    [11] Xue X.,Hanna K.,Abdelmoula M.,et al.Adsorption and oxidation of PCP on the surface of magnetite:Kinetic experiments and spectroscopic investigations.Applied Catalysis B:Environmental,2009,89(3-4):432-440
    [12] 吴德礼,段冬,马鲁铭.黄铁矿烧渣催化H2O2氧化废水中难降解污染物.化工学报,2010,61(4):1001-1008 Wu Deli,Duan Dong,Ma Luming.Fenton-like oxidation of refractory organic contaminants in wastewater using pyrite cinder at neutral pH.Journal of Chemical Industry and Engineering,2010,61(4):1001-1008(in Chinese)
    [13] Lin S.S.,Gurol M.D.Catalytic decomposition of hydrogen peroxide on iron oxide:Kinetics,mechanism,and implications.Environment Science and Technology,1998,32(10):1417-1423
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出版历程
  • 收稿日期:  2011-10-09
  • 刊出日期:  2012-10-16
冯勇, 吴德礼, 马鲁铭. 黄铁矿催化H2O2氧化降解水中三氯生[J]. 环境工程学报, 2012, 6(10): 3433-3437.
引用本文: 冯勇, 吴德礼, 马鲁铭. 黄铁矿催化H2O2氧化降解水中三氯生[J]. 环境工程学报, 2012, 6(10): 3433-3437.
Feng Yong, Wu Deli, Ma Luming. Catalytic oxidation of triclosan in water by pyrite and hydrogen peroxide[J]. Chinese Journal of Environmental Engineering, 2012, 6(10): 3433-3437.
Citation: Feng Yong, Wu Deli, Ma Luming. Catalytic oxidation of triclosan in water by pyrite and hydrogen peroxide[J]. Chinese Journal of Environmental Engineering, 2012, 6(10): 3433-3437.

黄铁矿催化H2O2氧化降解水中三氯生

  • 1. 同济大学环境科学与工程学院污染控制与资源化研究国家重点实验室, 上海 200092
基金项目:

国家自然科学基金资助项目(50808136)

上海科委长三角联合攻关项目(10195811400)

摘要: 以三氯生为目标污染物,研究了黄铁矿催化H2O2非均相类Fenton体系对污染物的去除效果,并利用SEM、EDS等手段对天然黄铁矿进行了表征。考察了催化剂、H2O2投加量、溶液初始pH、反应时间等重要因素对催化氧化反应的影响。在H2O2投加量5 mg/L,黄铁矿用量0.1 g/L,溶液初始pH为8,反应10 min后,三氯生的去除率达90%以上。相对于传统Fenton反应,pH对本非均相催化反应的影响较小,在2~10的pH范围内,仍有较高的催化活性。利用GC-MS分析显示,三氯生降解过程能够产生包括2,4-二氯苯酚在内的多种中间产物。

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