污水处理厂多环麝香污染物的分布特征及去除途径的初步研究
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摘要
合成麝香是天然麝香的廉价替代品,主要用在洗涤用品、化妆品、香水等中。
    根据结构的不同,合成麝香可分三大类:硝基麝香、多环麝香和大环麝香,其中
    应用得最广泛的是多环麝香,这些化合物随着人们的日常生活,如洗涤、沐浴等
    首先进入生活污水中。
     多环麝香与多环芳烃、多氯联苯等化合物性质相似,具有较强的亲脂、憎水
    性,容易吸附在有机物上,在环境中难降解,有很强的生物富集作用,呈现一定
    的雌激素活性。在污水处理过程中,水中的多环麝香极易吸附在水中的有机颗粒
    上,最后富集在污泥中;水中残留的多环麝香随着污水处理厂最后出水的排放而
    进入到环境水域中;富集在污泥中的多环麝香也会随着污泥的处理(应用到绿化
    草地或者填埋到地下)而进入到环境中。环境中的多环麝香会通过食物链富集在
    生物体内和人体内。环境科研工作者已经在各环境领域,如表层水、海水、水体
    沉积物、大气以及鱼、虾、贝类等生物样品中检测到了合成麝香,在人体脂肪组
    织、血液、乳汁中也检测出了相当含量的合成麝香。
     中国是生产合成麝香的大国之一,但对于环境中多环麝香的污染状况尚未展
    开研究。本研究借鉴多环芳烃、多氯联苯的分析方法,并参考外国文献报道的多
    环麝香的分析方法,建立了一套快速、简便、经济、实用的分析固体基质中多环
    麝香的分析方法和一套分析液态基质中多环麝香的分析方法。
     对三种类型的市政污水处理厂的外排污泥进行了初步的研究。GD1处理的
    是60%生活污水和40%工业废水的混合污水;GD2处理的主要是生活污水,GD3
    厂处理污水中70%是工业废水,包括一些日化产品生产厂家的生产废水以及30%
    的生活污水。从分析研究表明:在三个市政污水处理厂的外排污泥中,多环麝香
    含量相当高,其中:开许梅龙(DPMI)为0.599-2.870 mg/kg干污泥,萨利麝香
    (ADBI)为0.192—0.210 mg/kg干污泥,粉檀麝香(AHMI)为0.112.0.227 mg/kg
    干污泥(其中一个厂的样品中未检测出), 佳乐麝香(HHCB)为5.416-21.214
    mg/kg干污泥,吐纳麝香(AHTN)为0.715.6.195 mg/kg干污泥,在三个厂的
    样品中均未检测出特拉斯(ATII)。从实验结果可以看出,HHCB和AHTN是两
Synthetic musks, including nitro musks, polycyclic musks and macrocyclic musks, are inexpensive substitutes for natural musks. Polycyclic musks are representatives of synthetic musks. They are widespread used as fragrance materials in detergent, soap, cosmetic, perfume, shampoo, body lotion, personal care products, etc. These compounds enter domestic sewage after application.Polycyclic musks exhibit same properties, hydrophobic and lipophilic, bioaccumulation as polycyclic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). These nonpolar compounds prefer to be adsorbed to organic particles in water, are persistent in environmental and show weak estrogenic activity.Domestic sewage and industrial wastewater are treated in Wastewater Treatment Plants (WWTPs). Polycyclic musks enter environmental through sewage sludge (application to land, burial underground) and effluent from WWTPs. At last, polycyclic musks are bioaccumulated into biotas and human body through food chain. Researchers in environmental field have detected synthetic musks in almost every apartment of environmental, such as surface water, seawater, sediment, air and biota samples. Polycyclic musks have also been detected in human adipose tissues, blood and breast milk.Hitherto, little is known about the distribution and extent of possible contamination with the polycyclic musks in China, although China is one of the main countries producing synthetic musks. The aim of this study is developed a rapid, economic analytical method for polycyclic musks from solid matrix and from water.Sewgae sludge samples were collected from three municipal wastewater treatment plants (GD1, GD2, GD3), two household products plants (A, B) and one food plant (C). GD1 serves 700 thousand inhabitants with a daily capacity of 300,000 tons, of which 60% is domestic sewage, and 40% from industrial wastewaters. GD2 serves 1200 thousand inhabitants with a daily capacity of 220,000 tons, which primarily treats domestic sewage. GD3 serves 60 thousand inhabitants with a daily capacity of 30,000 tons and receives 30% domestic wastewater and 70% industrial
    wastewater including effluents from household products production.Polycyclic musks were Soxhlet extracted, separated and analyzed from these sludge samples using GC and GC-EI-MS. DPMI, ADBI, HHCB, AHTN are found in all samples, and ATII is not found in any sample. AHMI is detected in 5 out of 6 samples. HHCB and AHTN are the two major polycyclic musks found in highest concentrations in sludge. The sludge from 3 municipal wastewater treatment plants, contains HHCB, AHTN, ADBI, DPMI at concentrations between 5.416-21.214, 0.715-6.195, 0.192-0.210 and 0.599-2.870 mg/kg (dry), respectively. The highest concentration is found in sludge from a household products plant at 703.681 mg HHCB /kg (dry). The lowest concentrations of HHCB and AHTN are found in sludge from the food plant. The results indicate that, a) HHCB and AHTN are the two main components of polycyclic musks detected in sludge, b) there are two sources of polycylic musks: domestic sewage and industrial wastewater.The distribution of polycyclic musks in wastewater are analysed according to the treatment procedure in one municipal WWTP. The results indicate that influent (including 70% industrial wastewater and 30% domestic sewage) contains considerable concentration of polycyclic musks, most of which were adsorbed to the particles in wastewater, for example, more than 88% of HHCB and 82% of AHTN were adsorbed to the particles; The characteristic of distribution of polycyclic musks in primary effluent is similar to that in the influent. The main removal route of polycyclic musks from wastewater is adsorption to the organic particles in sludge, while oxidative degradation in activated sludge plays a minor role in the removal.
引文
1. C.Sommer. The role of musk and musk compounds in the fragrance industry. The Handbook of Environmental Chemistry Vol.3, Part Ⅹ, 2004:1-16
    2,白芸,天然麝香与合成麝香,广西轻工业,4:45-47,1994
    3.晁建平,杨春育,焦玉海,申宇太.张加来.粉檀麝香的合成研究.季精季料化妆品.3:5-6,4.2001
    4. G. G. Rimkus. Polycyclic musks fragrances in the aquatic environment. Toxicol. Lett. 111:37-56,1999
    5,闫朝阳,蔡清海.利用α-甲基苯乙烯合成佳乐麝香的研究.化学工程师 Sum88 (1):13-14;2002
    6,刘宇红.异色满类化合物香料化合物的合成及其进展.精细加工.11:24-27,1994
    7,汪多仁,合成吐纳麝香,化学世界,12:644-647,1995
    8,夏铮南,陆培溪.多环类合成麝香.上海轻工业.1:30-33;1992
    9,朴明福,大环状麝香,石油化工译丛,4:74-76,63,1989
    10. G. G. Rimkus, W. Butte, H. J. Geyer. Critical consideration on the analysis and bioaccumulation of musk xylene and other synthetic nitro musks in fish. Chemosphere 35 (7): 1497-1507, 1997
    11. G. G.Rimkus, M. Wolf. Nitro musk fragrance in biota from freshwater and marine environment. Chemosphere 30(4):641-651,1995
    12. C. Fernandez, M. Carballo, J. V. Tarazina.. A new method determine musk xylene inwater sewage fish and related products. Chemosphere 32(9):1805-1811,1996
    13. R. Gatermann, S. Biselli, H. Huhnerfuss, G. G. Rimkus, L.Karbe. Synthetic musks in the environment. Part Ⅰ: Species-dependent bioaccumulation of poiycyclic andnitro musk fragrances in freshwater fish. Arch. Environ. Contain. Toxicol.. 42:437-446, 2002
    14. D.R Hawkins, L.1 E Elsom, D. Kirkpatrick, R. A. Ford, A. M. Api. Dermal absorption and disposition of musk ambrette, musk ketone and musk xylene in human subjects. Toxico. Lett. 131:147-151,2002
    15. J. Riedel, W. Dekant. Biotransformation and toxicokinetics of musk xylene in humans. Toxicol. and Appl. Pharmacol. 157:145-155,1999
    16. P. Slanina. Risk evaluation of dietary and dermal exposure to musk fragrances. The Handbook of Environmental Chemistry.Vol. 3:Part x:281-310,2004
    17. T. Heberer. Occurrence, fate, and assessment of polycyclic musk resides in the aquatic environment of urban areas— a review. Acta hydrochim. Hydrobiol. 30(5-6):227-243,2002
    18. K. W. Schramm, A. Kaune, B.Beck, W. Thumm, A. Behechti,, A. Kettrup, P. Nickolova. Acute toxicities of five mtromusk compounds in Daphnia, Algae and photoluminescent Bacteria. Wat. Res. 30(10):2247-2250,1996
    19. R. Kallenborn, R. Gatermann. Synthetic Musks in ambient and indoor air. The Handbook of Environmental Chemistry Vol. 3, Part X: 85 - 104, 2004
    20. M. Ricking, J. Schwarzbauer, J. Hellou, A. Svenson, V. Zitko. Polycyclic aromatic musk compounds in sewage treatment plant effluents of Canada and Sweden—fiest results. Mar. Pollut. Bull. 46:410-417,2003
    21. F. Balk, R. A. Ford. Environmental risk assessment for the polycyclic musk AHTN and HHCB in the EU. I Fate and exposure assessment. Toxicol. Lett. 111:57-79,1999
    22. J. W. Tas, F. Balk, R.A. Ford, E. J. de Plassche. Environmental risk assessment of musk ketone and musk xylene in the Netherland in accordance with the EU-TGD. Chemosphere 35(12):2973-3002,1997
    23. L.Wollenberger, M. Breitholtz, K. O. Kusk, B.-E. Bengsson. Inhibition of larval development of the marine copepod Acartia tonsa by four synthetic musk substances. The Science of the Total Environment. 305:53-64,2003
    24. T. Yamagishi, T. Miyazaki, S. Horii, K.Akiyama. Identification of musk xylene and musk ketone in freshwater fish collected from the Tama River, Tokyo. Bull. Environ. Contam. Toxicol. 26,656-662,1981
    25. H. Fromme, T. Otto, K. Pilz. Polycyclic musk fragrance in different
     Environmental Compartment in Berlin (Germany). Wat . Res . 35 (1):121-128,2001
    26. C. Fooken. Synthetic musks in suspended particulate matters (SPM), sediment, and sewage sludge. The handbook environmental chemistry Vol. 3, Part X:29-47, 2004
    27. G G Rimkus, M. Wolf. Nitro musk fragrance in biota from freshwater and marine environment. Chemosphere 30(4) :641-651,1995
    28. L. Dsikowitzky, J. Schwarzbauer, R. Littke. Distribution of Polycyclic Musks in Water and Particulate Matter of the Lippe River (Germany). Org. Geochem. 33:1747-1758,2002
    29. M. Winkler, J.V. Headley, K. M. Peru . Optimization of solid-phase micraextraction for the gas chromatographic-mass spectrometric determination of synthetic musk fragrance in water samples. J. Chromatogr. A 903:203-210, 2000
    30. R. Gatermann, H. Huhnerfuss, G Rikmus, M. Wolf, S. Framke. The distribution of nitrobenzene and other nitroaromatic compounds in the North Sea. Mar. Pollu. Bull. 30(3):221-227,1995
    31. C. Garcia-Jares, M. Llompart, M. Polo, C. Salgado, S. Macias, R. Cela. Optimisation of a solid-phase microextraction method for synthetic musk compounds in water. J. Chromatogr. A 963:277-285,2002
    32. M. Winkler, G Kopf, C. Hauptvogel, T. Neu. Fate of artificial musk fragrance associated with suspended particulate matter (SPM) from the river Elbe(Germany) in comparison to other organic contaminants. Chemosphere 37(6):1139-1156,1998
    33. K. Bester, H. Huhnerfuss, W. Lange, G G Rimkus, N. Theobaild. Results of non target screening of lipophilic organic pollutants in the German Bight Ⅱ: Polycyclic musks fragrance. Wat. Res.. 32(6):1857-1863,1998
    34. I. J. Buerge, H.-R Buser, M. D. Muller, T. Poiger. Behavior of the polycyclic musks HHCB and AHTN in Lakes, Two potential anthropogenic markers for domestic wastewater in surface waters. Environ, Sci. Technol.
     37:5636-5644,2003
    35. E. M. J. Verbruggen, W. M. G M. Van Loon, M. Tonkes, P. V. Duijn, W. Seinen, J. L. M. Hermens. Biomimetric extraction as a tool to identify chemicals with high bioconcentration potential: An illustration by two fragrances in sewage treatment plant effluents and surface Waters. Environ. Sci. Technol. 33:801-806,1999
    36. T. Heberer, S. Gramer, H.-J. Stan. Occurrence and distribution of organic contamination in the aquatic system in Berlin. Part3: Determination of synthetic musks in Berlin surface water applying solid-phase rnicroextraction (SPME) and gas chromatography-mass spectrometry (GC-MS). Acta. Hydrochim. Hydrobiol. 27:150-156, 1999
    37. A. M. Peck, K. C. Hornbuckle . Synthetic musk frarances in lake Michigan. Environ. Sci. Technol. 38 (2):367-372, 2004
    38. L. I. Osemwengie, S. Steinberg. On-site solid-phase extraction and laboratory analysis of ultra-trace synthetic musks in municipal sewage effluent using gas chromatography-mass spectrometry in the full-scan mode. J. Chromatogra. A 932:107-118,2001
    39. J.-D. Berset, P. Bigler, D. Herren. Analysis of nitro musk compounds and their amino metabolites in liquid sewage sludge using NMR and spectrometry. Anal. Chem. 72:2124-2131,2000
    40. J. L. Stevens, G L. Northcott, G. A.Steven, G T. Tomy, K. C. Jones. PAHs, PCBs, PCNs, Organicchlorine Pestcides, synthetic musks,and polychlorinated n-Alkanes in U.K sewage sludge: survey results and implication. Environ .Sci. Technol. 37:462-467,2003
    41. D. Herren, J. D. Berset. Nitro musks, nitro musk amino metabolites and polycyclic musks in sewage sludges. Quantitative determination by HRGC-ion-trap-MS/MS and mass spectral characterization of the amino metabolites. Chemosphere 40:565-574,2000
    42. M. Llompart, C. Garcia-Jares, C. Salgado, Maria Polo, R. Cela. Determination of musk compounds in sewage treatment plant sludge samples by solid-phase
     microextract. J. chromatogr. A 999:185-193,2003
    43. T. A. ternes, J. Stuber, N. Herrmann, D. McDowell, A. Ried, Martin Kampmann, B. Teiser. Ozonation: a tool for removal of pharmaceuticals, contrast media and musk fragrance from wastewater? Wat. Res. 37:1976-1982,2003
    44. S. L. Simonich, T. W. Federle, W. S. Eckhoff, A. Rottiers, S. Webb, D. Sabaliunas, W. de Wolf. Removal of fragrance materials during U.S. and European wastewater treatment. Environ. Sci. Technol. 36:2839-2847,2002
    45. E. Artola-Garicano, I. Borkent, J. L. M. Hermens, W. H. J. Vaes. Removal of two polycyclic musks in sewage treatment plants: Freely dissolved and total concentrations. Environ. Sci. Technol. 37:3111-3116,2003
    46. S. L. Simonich, W. M. Begley, G Debaere, W. S. Bckhoff. Trace analysis of fragrance materials in wastewater and treated wastewater. Environ. Sci. Technol. 34:959-965,2000
    47. N. Paxeus. Organic pollutants in the effluents of large wastewater treatment plants in Sweden . Wat. Res. 30(5):l115-1122,1996
    48. T. Kupper, J. D. Berset, R. Etter-Holzer, R. Rurrer, J. Tarradellas. Concentrations and specific loads of polycyclic musks in sewage sludge originating from a monitoring network in Switzerland. Chemosphere 54:1111-1120,2004
    49. E. Artola-Garicano, J. L. M. Hermens, W.H. J. Vaes. Evaluation of simple treat 3.0 for two hydrophobic and slowly biodegradable chemicals: polycyclic musks HHCB and AHTN. Wat. Res. 37(18):4377-4384,2003
    50. W. Klopffer. Environmental hazard assessment of chemicals and products. Part V. Anthropogenic chemicals in sewage sludge. Chemosphere 33(6):1067-1081,1996
    51. R. Kallenborn, R. Gatemann, S. Planting, G G Rimkus. Gas chromatographic determination of synthetic musk compounds in Norwegian air samples. J. Chromatogr. A 846:295-306,1999
    52 R. Draisci, C. Marchiafava, E. Ferretti, L. Palleschi, G Catellani, A. Anastasio. Evaluation of musks contamination of frteshwater fish in Italy by accelerated solvent extraction and gas chromatography with mass spectrometric
     detection. J. Chromatogra. A 814:187-197,1998
    53. R. Gatermann, J. Hellou, H. Huhnerfuss, G Rikmus, V.Zitko. Polycyclic and nitro musks in the environment: A comparison between Canada and European aquitic biota. Chemosphere 38(14):3431-3441,1999
    54. S. Franke, C. Meyer, N. Heinzei, R. Gatermann, H. huhnerfuss, G. Rimkus, W. A. Konig, W. Francke. Enantiomeric composition of the polycyclic musks HHCB and AHTN in different aquatic species. Chirality 11:795-801,1999
    55. P. E. G. Leonards , J. de Boer. Synthetic musks in fish and other aquatic organisms. The Handbook of Environmental Chemistry Vol. 3, Part X: 49 - 84, 2004
    56. R. Gatermann, S. Biselli, H. Huhnerfuss, G G Rimkus, S. Franke, M. hecker,R. Kallenborn, L. Karbe. Synthetic musks in the environment. Part 2: enantioselective transformation of the polycyclic musk fragrances HHCB, AHTN, AHDI, and ATII in freshwater fish. Arch. Environ. Contarn. Toxicol. 42:447-453,2002
    57. L. I. Osemwengie, S. Steinberg. Closed-loop stripping analysis of synthetic musk compounds from fish tissues with measurement by gas chromatography-mass spectrometry with selected-ion monitoring. J. Chromatogr. A 993:1-15,2003
    58. H.-D. Eschke. Synthetic musks in different water matrices. The Handbook of Environmental Chemistry. Vol 3,Part X,17-28,2004
    59. J. Angerer, H. U. Kaffeerlein. Gas chromatographic method using electron-capture detection for the determination of musk xylene in human blood samples. Biological monitoring of the general population. J . Chromatogr . B 693:71-78,1997
    60. S. Muller, P. Schmid, C. Schlatter. Occurrence of nitro and non-nitro benzenoid musk compounds in human adpose tissue. Chemosphere 33(1):17-28,1996
    61. M. Ott, K. Failing, U. Lang, CH. Schubring, H.-J. Gent, S. Georgii, H. Brunn. Contamination of human milk in Middle Hesse, Germany-A cross-sectional study on the changing levels of chlorinated pesticides, PCB congeners and recent levels
     of nitro musks. Chemosphere 38(1)13-32,1999
    62. GG Rimkus, M. Wolf. Polycyclic musk fragrances in human adipose tissue and human milk. Chemosphere 33(10):2033-2043,1996
    63. M. Zehinger, A. Herrmann. Analysis of polychlorinated biphenyls, pyrethroid insecticides and fragrances in human milk using a cup laminar in the GC injector. Eur. Food Res. Technol. 212:247-251,2001
    64.H. U. Kafferlein, J. Angerer. Trends in the musk xylene concentrations in plasma samples from the general population from 1992/1993 to 1998 and relevance of dermal uptake. Int. Arch. Occup. Environ, Health. 74:470-476,2001
    65.J. riedel, W. decant. Biotransformation and toxicokinetics of musk xylene in humans. Toxicol. and Appl. Pharmacol. 157:145-155,1999
    66. F. Balk, R. A. Ford. Environmental risk assessment for the polycyclic musk AHTN and HHCB in the EU. II Effect assessment and risk charactersation. Toxicol. Lett. 111:81-94,1999
    67. L. J. Standley, L. A. Kaplan, D. Smith. Molecular tracers of organic matter to surface water resources. Environ. Sci. Technol. 34:3124-3130,2000
    68. A. Kronimus, J. Schwarzbauer, Larissa Dsikowitzky, S. Heim, R. Littke. Anthropogenic organic contaminants in sediments of the Lippe river, Germany. Wat. Res. 38 3473-3484, 2004
    69 P. Slanina. Risk evaluation of dietary and dermal exposure to musk fragrances. The Handbook of Environmental Chemistry., Vol.3 :Part x:281-310,2004
    70..R. A. Ford, D. R. Hawkins, R. Schwarzenbach, A. M. Api. The systemic exposure to the polycyclic musks, AHTH and HHCB, under condition of use as fragrance ingredients: evidences of lack of complete absorrtion from a skin reservoir. Toxicol. Lett. 111:133-142,1999
    71 A. M. Api, E. A. pfeitzer, R. H. San. An evaluation of genotoxicity tests with musk ketone. Food and Chemical Toxicicology 34:633-638,1996
    72.M. Emig, A.Reinhard, V. Mersch-Sundermann. A comparative study of five nitro musk conpounds for genotoxicity in the SOS chromatest and Salmonella
     mutagenicity. Toxicol. Lett. 85:151-156,1996
    73.P.S. Spencer, M.C. Bischoff-Fenton, OM. Moreno, D.L.Opdyke, R.A. Ford. Neurotoxic properties of musk ambrette. Toxicol. Appl. Pharmacol. 75:571-575,1984
    74. J.C. Spain. Biodegradation of nitroaromatic compounds. Annu. Rev. Microbiol. 49:523-555,1995
    75. S. Minegishi, S. Fukuoka, A. tanaka, T. Nishimakimogami. Distribution, metabolism, and excretion of musk xylene in rats. Arch. Toxicol. 65:273-282, 1991
    76. A.Behechti, K. W. schramm, A. Attar, J. Niederfellner , A. Kettrup. Acute aquatic toxicities of four musk xylene derivatives on Daphnia Magna. Wat. Res., 32(5): 1704-1707,1998
    77. J .M Giddings, D. Salvito, A. E. Putt. Acute toxicity of 4-animo- musk xylene to Daphnia magna in laboratory water and natural water. Wat. Res. 34(14):3686-3689.2000
    78. H. Brunn, N. Bitsch, J. A. Muller. Toxicology of synthetic musk compounds in man and animals. The handbook of environmental chemistry Vol.3, Part X:259-280,2004
    79. A. M. Api, R. A. Ford. Evaluation of the oral subchronic toxicity of HHCB (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-g-2- benzopyran) in the rat. Toxicol. Lett. 111 : 143-149, 1999
    80. M. S. Christian , R. M. Parker, A. M. Hoberman, R. M. Diener , A. M. Api. Developmental toxicity studies of four fragrances in rats. Toxicol. Lett. 111 : 169-174, 1999
    81. N. Apinipes, M. Breitholtz , L. Wollenberger, L. Dinan. Effects of four synthetic musks on the life cycle of the harpacticoid copepod. Aquatic Toxicology 63: 103-118,2003
    82 P. Steinberg, T. Fischer, M. Arand, E. Park, I. Elmadfa, G. Rimkus, H. Brunn, H.-P. Dienes. Acute hepatotoxicity of the polycyclic musk 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthaline(AHTN).
     Toxicol. Lett. 111: 151-160, 1999
    83. M. Y. Fukayama, O. D. Easterday, P. A. Serafino, K. J. Renskers, H. North-Root, K. R. Schrankel. Subchronic inhalation studies of complex fragrance mixtures in rats andhamsters. Toxicol. Lett. 111: 175-187, 1999
    84. N. Bitsch, C. Dudas, W. Komer, K. Failing, S. Biselli, G. Rimkus, H. Brunn. Estrogenic activity of musk rfangrances detected by the E-screen assary using human MCF-7 cells. Arch.Environ.Contam. Toxicol. 43:257-264,2002
    85. W. Seinen, J. G. Lemmen, R. H. H. Pieters, E. M.J. Verbruggen, B. van der Burg. AHTN and HHCB show weak estrogenic—but no uterotrophic activity. Toxicol. Lett. 111: 161-168, 1999
    86. T. Luckenbach, D. Epel. Nitromusk and polycyclic musk compounds as long-term inhibitors of cellar xenobiotic defense systems mediated by multidrug transporters. Environl Health Perspect. 113:17-24,2005
    87. T. Luckenbach, I. Corsi, D. Epel. Fatal attraction: synthetic muskfragrances compromise multixenobiotic defense systems in mussels. Mar. Environ. Res. 58:215-219,2004
    88.罗孝俊.珠江三角洲河流、河口和邻近南海海域水体、沉积物中的多环芳烃与有机氯农药研究.博士学位论文。2004,7
    89.樊祥熹.环境分析.首都师范大学出版社.1995
    90. P. Enoch, A. Putzler, D. Rirme, J. Schluter. Automated solid-phase extraction on-line coupled to gas chromatography. J. Chromatogr. A 822:75-82,1998
    91. T. A. Temes, M. Bonerza, N. Herrmanna, D. Loffiera, E. Kellerb, B. B. Lacidab, A. C. Alderb. Determination of pharmaceuticals, iodinated contrast media and musk fragrances in sludge by LC tandem MS and GC/MS. J. Chromatogr. A (In Press), Available online,28, November, 2004
    92.林春绵,蔚立玉,王军良,陈钦安.城市污水处理厂污泥的肥料化应用.浙江工业大学学报.32(2):151-156,2004
    93.翟云波,魏先勋,曾光明,张德见.城市污水处理厂污泥资源化利用途径探讨.工业水处理.24(2):8-11
    94.赵乐军,杨津义.污泥填埋技术综述.天津市政设计.3:13-17,2003
    95.刘莲香,张涛.污水处理厂污泥在建材生产中的综合应用.砖瓦 5:12-13,2004
    96.郝薇.污水处理厂对周边环境的污染及治理. 给水排水 30(4):15-18,2004
    97.赵进英,李金昶.固相萃取技术及其在环境分析中的应用.化学工程师 Sup90(6):29-31,2002
    98.董玉瑛,孙成,王晓栋,王连生.固相萃取技术在水体有机物分析中的应用.环境科学学报 7(4):83-90,1999
    99.胡振元,施梅儿.痕量环境有机污染物分析中的样品前处理技术.化学世界 11:563-574,1999
    100.黄骏雄.环境样品前处理技术及其进展(一).环境化学 13(1):95-105,1995
    101.黄骏雄.环境样品前处理技术及其进展(一).环境化学 13(2):181-193,1995
    102.潘海祥,麦碧娴,庄汉平,林峥,闵育顺,盛国英,傅家谟.使用C_(18)固相萃取膜-色质联用定量分析饮用水中痕量多环芳烃的初步研究.分析化学 27(2):140-144,1999
    103.张月琴,吴淑琪.水中有机污染物前处理方法进展.分析测试学报 22(3):106-109,2003
    104.王梅,张莘民.我国环境中有机污染物分析方法及痕量富集技术的进展.环境监测管理与技术 16(1):13-16,2004
    105.任丽萍,田芹,刘丰茂,江树人,王平,刘承兰.固相萃取和气相色谱技术测定环境水体中痕量农药.中国农业大学学报 9(2):93-96,2004
    106.张海霞,朱彭龄.固相萃取.分析化学 28(9):1172-1180;2000
    107.王立,汪正范,牟世芬,丁晓静.色谱分析样品处理.化学工业出版社,84-97,2001
    108.田晶,翟滨,于玲.固相萃取法固定相的选择原则.大连轻式业学院学报 15(4):41-44,1996
    109.楼蔓藤,商振华.固相萃取技术的发展与应用.分析仪器 1:1-6,1998
    110.彭晓峰,陶涛,陈剑波,朱敬平,李笃中.国际污泥研究现状初探.自然杂志 24(4):191-194;2002
    111.张守君,杜永林.污水处理中污泥处理技术分析.云南环境科学 20(4):40-41;2001
    112.陈涛,王军.城市环境的一大课题——污水处理厂污泥处置浅析.环境保护科学 24(6)11-12,1998
    113.吴吉夫,王淑坤,臧树良.城市污水处理厂污泥的有效利用和相关的环境问题研究.辽宁大学学报(自然科学版) 29(1):90-92,2002
    114.叶子瑞.国内外污泥处置和管理现状.环境卫生工程 10(2):85-88,2002
    115.李进,毛成利,白凤君.污泥的特性与处理.化学工程师 Sum89(2):31-32,2002
    116.胡金杰.污泥和废水土地处理法增加农作物产量.中国皮革 32(5):46,2003
    117.王新,周启星,陈涛,葛英华,台培东.污泥土地利用对草坪草及土壤的影响.环境科学 24(2):50-53,2003
    118.曹秀芹,陈君.污水处理厂污泥处理存在问题分析.北京建筑工程学院学报 18(1):1-4,2002
    119.周雹.国内外城市污水处理概况.天津市政设计 3&4:74-89,2003
    120.田静,张捷.关于我国城市污水处理产业化的思考.中国工程咨询 42:36-37,2004
    121.吴晓霞,张雁秋,何士龙.浅谈城市污水处理在可持续发展中的作用.甘肃环境研究与监测 16(4):402-405,2003
    122.计建洪.水域污染治理的思路探讨.化工时刊 17(12):14-16,2003
    123.王洪斌.城市居民生活污水再利用.环境保护 3:74,2004
    124. K. Bester. Retention characteristics and balance assessment for two polycyclic musk fragrances (HHCB and AHTN) in a typical German sewage treatment plant. Chemosphere 57: 863-870, 2004
    125. T. A. Temes, N. Herrmann, M. Bonerz, T. Knacker, H. Siegrist, A. Joss. A rapid method to measure the solid - water distribution coefficient (K_d) for Pharmaceuticals and musk fragrances in sewage sludge. Wat. Res. 38:4075 - 4084,2004
    126. H. Huhnerfuss, S. Biselli, R. Gatermann, R. Kallenborn, G.G.Rimkus. Enantioselective analysis of the HHCB metabolite galaxolidone in environmental samples. Organohal. Compd. 52: 441—444.2001.

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