持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析

韦朝海, 张小璇, 任源, 胡芸, 吴海珍. 持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析[J]. 环境化学, 2011, 30(1): 300-309.
引用本文: 韦朝海, 张小璇, 任源, 胡芸, 吴海珍. 持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析[J]. 环境化学, 2011, 30(1): 300-309.
WEI Chaohai, ZHANG Xiaoxuan, REN Yuan, HU Yun, WU Haizhen. POLLUTION CONTROL OF PERSISTENT ORGANIC POLLUTANTS IN WATER SYSTEM: ADSORPTION/ENRICHMENT, BIODEGRADATION AND PROCESS ANALYSIS[J]. Environmental Chemistry, 2011, 30(1): 300-309.
Citation: WEI Chaohai, ZHANG Xiaoxuan, REN Yuan, HU Yun, WU Haizhen. POLLUTION CONTROL OF PERSISTENT ORGANIC POLLUTANTS IN WATER SYSTEM: ADSORPTION/ENRICHMENT, BIODEGRADATION AND PROCESS ANALYSIS[J]. Environmental Chemistry, 2011, 30(1): 300-309.

持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析

  • 基金项目:

    国家自然科学基金项目(No. 20777018,20977035,21037001)

    "十一五"国家科技支撑计划重点项目(No. 2008BAC32B06-1)资助.

POLLUTION CONTROL OF PERSISTENT ORGANIC POLLUTANTS IN WATER SYSTEM: ADSORPTION/ENRICHMENT, BIODEGRADATION AND PROCESS ANALYSIS

  • Fund Project:
  • 摘要: 介绍了持久性有机污染物(POPs)的定义、来源以及我国涉及POPs的工业生产与数量分布,明确氯碱工业、有机氯工业等精细化工业与垃圾焚烧厂产生的POPs成为未来的主要污染源;对统计数据进行分析指出,由于历史上POPs的应用以及排放,我国工业发达地区河段水体中普遍检出POPs,浓度为几到几十ng·L-1范围,部分流域超标;针对水体中低剂量的POPs,吸附法是有效的分离技术,生物相及仿生吸附剂具有较高的富集倍数;POPs的生物降解在热力学方面被认为可行,高效菌不断地被分离得到,因此,吸附富集与功能微生物细胞固定化技术的耦联可以成为有效的控制技术;此外,还从以清洁生产为目标的源头控制、POPs的广泛监控和政策落实方面评价了POPs的控制过程.最后指出,POPs的水污染控制应当立足于科学、技术与工业过程研究的结合.
  • 加载中
  • [1] White R, Jobling S, Hoare S A, et al. Environmentally persistent alkylphenolic compounds are estrogenic [J]. Endocrinology, 1994, 135: 175-182
    [2] Decision 18/32 of the UNEP Governing Council: Persistent organic pollutants. Geneva, Switzerland, 1995
    [3] Zhu J, Hirai Y, Sakai S, et al. Potential source and emission analysis of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in China [J]. Chemosphere, 2008, 73: S72-S77
    [4] Zheng G J, Leung A O W, Jiao L P, et al. Polychlorinated dibenzo-p-dioxins and dibenzofurans pollution in China: Sources, environmental levels and potential human health impacts [J]. Environment International, 2008, 34: 1050-1061
    [5] 曹启民, 王华, 张黎明, 等. 中国持久性有机污染物污染现状及治理技术进展[J]. 中国农学通报, 2006, 22(2): 361-365
    [6] Xing G H, Chan J K Y, Leung A O W, et al. Environmental impact and human exposure to PCBs in Guiyu, an electronic waste recycling site in China [J]. Environment International, 2009, 35: 76-82
    [7] 邢颖, 吕永龙, 史雅娟, 等. 我国二噁英和多氯联苯的研究现状及对策分析[J]. 环境保护科学, 2006, 32(5): 33-35
    [8] 华小梅, 单正军. 我国农药的生产,使用状况及其污染环境因子分析[J]. 环境科学进展, 1996, 4(2): 33-45
    [9] Yang R, Yao T, Xu B, et al. Distribution of organochlorine pesticides (OCPs) in conifer needles in the southeast Tibetan Plateau [J]. Environmental Pollution, 2008, 153(1): 92-100
    [10] Zhang G, Parker A, House A, et al. Sedimentary records of DDT and HCH in the Pearl River delta, south China [J]. Environmental Science and Technology, 2002, 36(17): 3671-3677
    [11] 任仁, 《斯德哥尔摩公约》禁用的12种持久性有机污染物[J]. 大学化学, 2003, 18 (3): 37-41
    [12] Xing Y, Lu Y L, Dawson R W, et al. A spatial temporal assessment of pollution from PCBs in China [J]. Chemosphere, 2005, 60 (6): 731-739
    [13] 包志成. 五氯酚及其钠盐中二噁英的分析[J]. 环境化学,1995,14:317-321
    [14] 金重阳, 郑玉峰, 黄相国, 等. 国内持久性有机污染物的污染现状与对策建议[J]. 环境保护科学, 2002, 28(11): 30-31
    [15] 黄俊, 余刚, 钱易. 我国的持久性有机污染物问题与研究对策[J]. 环境保护, 2001, 11: 3-6
    [16] 薛祖源. 我国氯碱行业生产发展评析[J]. 中国氯碱, 2007, (12): 1-6
    [17] 徐盈, 张庆华, 吴文忠, 等. 我国某厂石墨电极废渣中二噁英的指纹特征[J]. 科学通报, 2000, 45(6): 578-583
    [18] 中华人民共和国国家统计局. 中国统计年鉴2009 . 2010-5-23
    [19] 中华人民共和国国家统计局. 中华人民共和国2009年国民经济和社会发展统计公报 . 2010-05-21
    [20] 世界银行. 世界发展指标2008
    [21] Gao J, Liu L, Liu X, et al. Occurrence and distribution of organochlorine pesticides-lindane, p,p'-DDT, and heptachlor epoxide-in surface water of China [J]. Environment International, 2008, 34: 1097-1103
    [22] Zhou R B, Zhu L Z, Chen Y Y, et al. Concentrations and characteristics of organochlorine pesticides in aquatic biota from Qiantang River in China [J]. Environmental Pollution, 2008, 151: 190-199
    [23] Zhou J L, Hong H, Zhang Z, et al. Multi-phase distribution of organic micropollutants in Xiamen Harbour, China [J]. Water Research, 2000, 34(7): 2132-2150
    [24] 杨清书, 麦碧娴, 傅家谟, 等. 珠江干流河口水体有机氯农药的研究[J]. 中国环境科学, 2005, 25 (6): 47-51
    [25] 杨清书, 麦碧娴, 罗孝俊, 等. 珠江澳门水域水柱多环芳烃初步研究[J]. 环境科学研究, 2004, 17 (3): 28-33
    [26] 皇冠星, 孙继朝, 汪珊, 等. 珠江三角洲地下水有机氯农药分布特征的初探[J]. 农业环境科学学报, 2008, 27(4): 1471-1475
    [27] Zhang Z L, Hong H S, Zhou J L, et al. Fate and assessment of persistent organic pollutants in water and sediment from Minjiang River estuary, southeast China[J]. Chemosphere, 2003, 52 (9): 1423-1430
    [28] 张祖麟, 陈伟琪, 哈里德, 等. 九龙江口水体中有机氯农药分布特征及归宿[J]. 环境科学, 2001, 22 (3): 88-92
    [29] 夏凡, 胡雄星, 韩中豪, 等. 黄浦江表层水体中有机氯农药的分布特征[J]. 环境科学研究, 2006, 19 (2): 11-15
    [30] 张菲娜, 祁士华, 苏秋克, 等. 福建兴化湾水体有机氯农药污染状况[J]. 地质科技情报, 2006, 25 (4): 86-91
    [31] 胡雄星, 夏德祥, 韩中豪, 等. 苏州河水及沉积物中有机氯农药的分布和归宿[J]. 中国环境科学, 2005, 25 (1): 124-128
    [32] 杨梅, 张俊鹏, 蒲俊兵, 等. 重庆典型岩溶区地下河水体有机氯农药污染初步研究[J]. 中国岩溶, 2009, 28 (2): 144-148
    [33] 万译文, 康天放, 周忠亮, 等. 北京官厅水库中有机氯类农药的分布和来源[J]. 生态与农村环境学报, 2009, 25 (1): 53-56

    , 68

    [34] 窦薇, 赵忠宪. 白洋淀水体、底泥及鲫鱼体内DDT、BHC污染状况研究[J]. 环境科学学报, 1998, 18 (3): 308-312
    [35] 王泰, 张祖麟, 黄俊, 等. 海河与渤海湾水体中溶解态多氯联苯和有机氯农药污染状况调查[J]. 环境科学, 2007, 28 (4): 730-735
    [36] 金重阳, 刘辉, 荆志严. 活性炭纤维处理含多氯联苯废水的研究[J]. 环境保护科学, 1997, 23(3): 6-7
    [37] Pavoni B, Drusian D, Giacometti A, et al. Assessment of organic chlorinated compound removal from aqueous matrices by adsorption on activated carbon [J]. Water Research, 2006, 40: 3571-3579
    [38] Aksu Z, Kabasakal E, Batch adsorption of 2,4-dichlorophenoxy-acetic acid (2,4-D) from aqueous solution by granular activated carbon [J]. Separation and Purification Technology, 2004, 35: 223-240
    [39] Oliveira L C A, Rios R V R A, Fabris J D, et al. Activated carbon/iron oxide magnetic composites for the adsorption of contaminants in water [J]. Carbon, 2002, 40: 2177-2183
    [40] 张小璇, 任源, 贺明和, 等. 污水处理厂尾水中有机氯化物的活性炭吸附深度处理[J]. 环境科学学报, 2009, 29(3): 548-554
    [41] 张小璇, 任源, 韦朝海, 等. 焦化废水生物处理尾水中残余有机污染物的活性炭吸附及其机理[J]. 环境科学学报, 2007, 27(7): 1113-1120
    [42] 舒月红, 贾晓珊. CTMAB-膨润土从水中吸附氯苯类化合物的机理——吸附动力学与热力学[J]. 环境科学学报, 2005, 25 (11): 1530-1536
    [43] 朱利中, 陈宝梁, 罗瑜. 有机膨润土吸附水中多环芳烃的性能及机理研究[J]. 环境科学学报, 2000, 20 (1): 21-25
    [44] 郭照冰, 郑寿荣, 郑正, 等. MFI型沸石吸附分离水体中混合硝基氯苯的研究[J]. 环境科学学报, 2005, 25 (6): 773-778
    [45] 郭伟群, 任世建. 用粉煤灰吸附硝基氯苯废水的方法[J]. 中国氯碱, 2002, (9): 41-42
    [46] 杨旭, 俞飞. 树脂吸附法处理硝化废水[J]. 污染防治技术, 2007, 20 (3): 9-12

    , 78

    [47] Sennour R, Mimane G, Benghalem A, et al. Removal of the persistent pollutant chlorobenzene by adsorption onto activated montmorillonite [J]. Applied Clay Science, 2009, 43: 503-506
    [48] Gupta V K, Ali I, Suhas, et al. Adsorption of 2,4-D and carbofuran pesticides using fertilizer and steel industry wastes [J]. Journal of Colloid and Interface Science, 2009, 333(1): 14-26
    [49] Katsoyiannis A, Samara C. Persistent organic pollutants (POPs) in the conventional activated sludge treatment process: fate and mass balance [J]. Environmental Research, 2005, 97: 245-257
    [50] Aksu Z. Application of biosorption for the removal of organic pollutants: a review [J]. Process Biochemistry, 2005, 40: 997-1026
    [51] Zhang X, Wei C, He Q, et al. Enrichment of chlorobenzene and o-nitrochlorobenzene on biomimetic adsorbent prepared by poly-3-hydroxybutyrate (PHB) [J]. Journal of Hazardous Materials, 2010, 177: 508-515
    [52]
    [53] 茹加, 刘会娟, 曲久辉等. 类脂复合吸附剂去除水中微量七氯和环氧七氯的研究[J]. 环境科学学报, 2006, 26(11): 1757-1762
    [54] 董玉瑛, 冯霄. 持久性有机污染物分析和处理技术研究进展[J]. 环境污染治理技术与设备, 2003, 4(6): 49-55
    [55] Pieper D H. Aerobic degradation of polychlorinated biphenyls [J]. Applied Microbiology and Biotechnology, 2005, 67 (2): 170-191
    [56] Quintero J C, Moreira M T, Feijoo G, et al. Anaerobic degradation of hexachlorocyclohexane isomers in liquid and soil slurry systems [J]. Chemosphere, 2005, 61:528-536
    [57] Janssen D B, Oppentocht J E, Poelarends G J. Microbial dehalogenation [J]. Current Opinion Biotechnology, 2001, 12 (3): 254-258
    [58] Adrian L, G risch H, Microbial transformation of chlorinated benzenes under anaerobic conditions [J]. Research in Microbiology, 2002, 153 (3): 131-137
    [59] Guerin T F. Ex-situ bioremediation of chlorobenzenes in soil [J]. Journal of Hazardous Materials, 2008, 154 (1/3): 9-20
    [60] Adebusoye S A, Picardal F W, Ilori M O, et al. Aerobic degradation of di- and trichlorobenzenes by two bacteria isolated from polluted tropical soils [J]. Chemosphere, 2007, 66 (10): 1939-1946
    [61] Spain J C, Nishino S F. Degradation of 1,4-dichlorobenzene by a Pseudomonas sp. [J]. Applied and Environmental Microbiology, 1987, 53(5): 1010-1019
    [62] Monferrán M V, Echenique J R, Wunderlin D A. Degradation of chlorobenzenes by a strain of Acidovorax avenae isolated from a polluted aquifer [J]. Chemosphere, 2005, 61: 98-106
    [63] Nishino S F, Spain J C, Belcher L A, et al. Chlorobenzene degradation by bacteria isolated from contaminated groundwater [J]. Applied and Environmental Microbiology, 1992, 58(5): 1719-1726
    [64] Morasch B, Richnow H H, Vieth A, et al. Stable isotope fractionation caused by glycyl radical Enzymes during bacterial degradation of aromatic compounds [J]. Applied and Environmental Microbiology, 2004, 70 (5): 2935-2940
    [65] Tiedje J M, Quensen J F, Chee-Sanford J, et al. Microbial reductive dechlorination of PCBs [J].Biodegradation, 1993, 4(4): 231-240
    [66] Nies L, Vogel T M. Effects of organic substrates on dechlorination of aroclor 1242 in anaerobic sediments [J]. Applied Environmental Microbiology, 1990, 56(9): 2612-2617
    [67] Brown T M, Sheldon T A, Burgess N M, et al. Reduction of PCB contamination in an arctic coastal environment: a first step in assessing ecosystem recovery after the removal of a point source [J]. Environmental Science and Technology, 2009, 43(20): 7635-7642
    [68] Dort H M, Smullen L A, May R J, et al. Priming microbial meta-dechlorination of polychlorinated biphenyls that have persisted in Housatonic River sediments for decades [J]. Environmental Science and Technology, 1997, 31(11): 3300-3307
    [69] Cho Y C, Ostrofsky E B, Sokol R C, et al. Enhancement of microbial PCB dechlorination by chlorobenzoates, chlorophenols and chlorobenzenes [J]. FEMS Microbiology Ecology, 2002, 42(1): 51-58
    [70] Fennell D E, Nijenhuis I, Wilson S F, et al. Dehalococcoides ethenogenes strain 195 reductively dechlorinates diverse chlorinated aromatic pollutants [J]. Environmental Science and Technology, 2004, 38(7): 2075-2081
    [71] May H D, Miller G S, Kjellerup B V, et al. Dehalorespiration with olychlorinated biphenyls by an anaerobic ultramicrobacterium [J]. Applied and Environmental Microbiology, 2008, 74(7): 2089-2094
    [72] Borja J, Taleon D M, Auresenia J, et al. Polychlorinated biphenyls and their biodegradation [J]. Process Biochemistry, 2005, 40: 1999-2013
    [73] Lorbeer H, Starke S, Gozan M, et al. Bioremediation of chlorobenzene-contaminated groundwater on granular activated carbon barriers [J]. Water, Air, and Soil Pollution: Focus, 2002, 3: 183-193
    [74] 周盛, 韦朝海. 活性污泥中功能性优势未培养微生物的强化与检测研究进展[J]. 化工进展, 2008, 27(8): 1204-1209.
    [75] 曹艳娜, 张安龙. 造纸废水中有机氯化物毒性的研究进展[J]. 西南造纸, 2006, 35(5): 18-20
    [76] Taylor P H, Lenoir D. Chloroaromatic formation in incineration processes [J]. The Science of the Total Environment, 2001, 269: 1-24
    [77] 牛军峰, 余刚, 刘希涛. 水相中POPs光化学降解研究进展[J]. 化学进展, 2005, 17(5): 938-948
    [78] 夏传海, 徐杰, 吴文忠, 等. 二噁英降解方法的研究[J]. 化学进展, 2004, 16(1): 123-130
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  • 收稿日期:  2010-06-24
韦朝海, 张小璇, 任源, 胡芸, 吴海珍. 持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析[J]. 环境化学, 2011, 30(1): 300-309.
引用本文: 韦朝海, 张小璇, 任源, 胡芸, 吴海珍. 持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析[J]. 环境化学, 2011, 30(1): 300-309.
WEI Chaohai, ZHANG Xiaoxuan, REN Yuan, HU Yun, WU Haizhen. POLLUTION CONTROL OF PERSISTENT ORGANIC POLLUTANTS IN WATER SYSTEM: ADSORPTION/ENRICHMENT, BIODEGRADATION AND PROCESS ANALYSIS[J]. Environmental Chemistry, 2011, 30(1): 300-309.
Citation: WEI Chaohai, ZHANG Xiaoxuan, REN Yuan, HU Yun, WU Haizhen. POLLUTION CONTROL OF PERSISTENT ORGANIC POLLUTANTS IN WATER SYSTEM: ADSORPTION/ENRICHMENT, BIODEGRADATION AND PROCESS ANALYSIS[J]. Environmental Chemistry, 2011, 30(1): 300-309.

持久性有机污染物的水污染控制:吸附富集、生物降解与过程分析

  • 1.  华南理工大学环境科学与工程学院, 广州, 510006;
  • 2.  华南理工大学生物科学与工程学院, 广州, 510006;
  • 3.  安徽师范大学化学与材料科学学院, 芜湖, 241000
基金项目:

国家自然科学基金项目(No. 20777018,20977035,21037001)

"十一五"国家科技支撑计划重点项目(No. 2008BAC32B06-1)资助.

摘要: 介绍了持久性有机污染物(POPs)的定义、来源以及我国涉及POPs的工业生产与数量分布,明确氯碱工业、有机氯工业等精细化工业与垃圾焚烧厂产生的POPs成为未来的主要污染源;对统计数据进行分析指出,由于历史上POPs的应用以及排放,我国工业发达地区河段水体中普遍检出POPs,浓度为几到几十ng·L-1范围,部分流域超标;针对水体中低剂量的POPs,吸附法是有效的分离技术,生物相及仿生吸附剂具有较高的富集倍数;POPs的生物降解在热力学方面被认为可行,高效菌不断地被分离得到,因此,吸附富集与功能微生物细胞固定化技术的耦联可以成为有效的控制技术;此外,还从以清洁生产为目标的源头控制、POPs的广泛监控和政策落实方面评价了POPs的控制过程.最后指出,POPs的水污染控制应当立足于科学、技术与工业过程研究的结合.

English Abstract

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