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受原始技术电子垃圾回收影响的中国贵屿地区土壤中多环芳烃的分布。

Distribution of polycyclic aromatic hydrocarbons in soils at Guiyu area of China, affected by recycling of electronic waste using primitive technologies.

作者信息

Yu X Z, Gao Y, Wu S C, Zhang H B, Cheung K C, Wong M H

机构信息

Croucher Institute for Environmental Sciences, Department of Biology, Hong Kong Baptist University, Kowloon Tong, Hong Kong.

出版信息

Chemosphere. 2006 Nov;65(9):1500-9. doi: 10.1016/j.chemosphere.2006.04.006. Epub 2006 May 19.

DOI:10.1016/j.chemosphere.2006.04.006
PMID:16713614
Abstract

The concentration, distribution, profile and possible source of polycyclic aromatic hydrocarbons (PAHs) in soil were studied in Guiyu, an electronic waste (E-waste) recycling center, using primitive technologies in Southeast China. Sixteen USEPA priority PAHs were analyzed in 49 soil samples (0-10 cm layer) in terms of individual and total concentrations, together with soil organic matter (SOM) concentrations. The concentrations of a sum of 16 PAHs ranged from 44.8 to 3206 microgkg(-1) (dry weight basis), in the descending order of E-waste open burning sites (2065 microgkg(-1))>areas near burning sites (851microgkg(-1))>rice fields (354 microgkg(-1))>reservoir areas (125microgkg(-1)). The dominant PAHs were naphthalene, phenanthrene and fluoranthene, which were mainly derived from incomplete combustion of E-waste (e.g. wire insulations and PVC materials), and partly from coal combustion and motorcycle exhausts. All individual and total PAH concentrations were significantly correlated with SOM except for naphthalene and acenaphthylene. Principal component analysis was performed, which indicated that PAHs were mainly distributed into three groups in accordance with their ring numbers and biological and anthropogenic source. In conclusion, PAH concentrations in the Guiyu soil were affected by the primitive E-waste recycling activities.

摘要

在中国东南部,采用原始技术的电子垃圾(电子废弃物)回收中心贵屿,对土壤中多环芳烃(PAHs)的浓度、分布、特征及可能来源进行了研究。对49个土壤样本(0 - 10厘米土层)中的16种美国环保署优先控制的多环芳烃进行了分析,测定了其各自的浓度和总浓度,同时还测定了土壤有机质(SOM)的浓度。16种多环芳烃的总浓度范围为44.8至3206微克/千克(干重),从高到低依次为:电子垃圾露天焚烧场地(2065微克/千克)>焚烧场地附近区域(851微克/千克)>稻田(354微克/千克)>水库区域(125微克/千克)。主要的多环芳烃为萘、菲和荧蒽,它们主要来源于电子垃圾的不完全燃烧(如电线绝缘材料和聚氯乙烯材料),部分来源于煤炭燃烧和摩托车尾气排放。除萘和苊烯外,所有多环芳烃的各自浓度和总浓度均与土壤有机质显著相关。进行了主成分分析,结果表明,多环芳烃主要根据其环数以及生物和人为来源分为三组。总之,贵屿土壤中的多环芳烃浓度受到原始电子垃圾回收活动的影响。

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