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中国南方一个密集型电子废物回收场的灰尘、土壤、沉积物中多氯二苯并对二恶英和多氯二苯并呋喃(PCDD/Fs)的空间分布及健康风险评估。

Spatial distribution of polychlorinated dibenzo-p-dioxins and dibenzo-furans (PCDDs/Fs) in dust, soil, sediment and health risk assessment from an intensive electronic waste recycling site in Southern China.

机构信息

State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China.

出版信息

Environ Sci Process Impacts. 2013 Oct;15(10):1889-96. doi: 10.1039/c3em00319a.

DOI:10.1039/c3em00319a
PMID:23955158
Abstract

Workshop dust, soil and sediment samples were collected to investigate the level and spatial distribution of PCDDs/Fs at an intensive electronic waste (e-waste) recycling site in Southern China, and also to characterize the dioxin emission in different e-waste recycling procedures. The concentrations of total PCDDs/Fs ranged from 1866 to 234292 ng kg(-1) for the dust samples, from 3187 to 63998 ng kg(-1) dry wt for the top soils, and 33718 ng kg(-1) for the surface sediment. All the samples were characterized by abnormally high concentrations of OCDD and an extremely low portion of PCDFs. Different e-waste recycling procedures may generate different congener profiles. Open burning and dismantling were the two procedures emitting relatively higher concentrations of PCDDs/Fs in this case, indicating that low-tech recycling operations were one of the major contributors of PCDDs/Fs to the environment. The variation and distinction of the concentrations and homologue/congener profiles among different environmental matrices reveal the characteristics of contaminant environmental behavior and fate during the transportation from "source" to "sink". Daily intake of PCDDs/Fs through soil ingestion and dermal absorption was negligible, but the rough estimated total PCDD/F intake dose far exceeded the tolerance daily intake value of 4 pg-TEQ per kg per day recommended by WHO, indicating that residents in Longtang were at a high risk of exposure to dioxins, especially children.

摘要

工作坊粉尘、土壤和沉积物样本被采集,以调查中国南方一个密集型电子废物(电子废物)回收场的多氯二苯并对二恶英/呋喃(PCDD/Fs)的水平和空间分布情况,并对不同电子废物回收过程中的二恶英排放情况进行特征描述。粉尘样本中总 PCDD/Fs 的浓度范围为 1866 至 234292ngkg(-1),表层土壤中的浓度范围为 3187 至 63998ngkg(-1)干重,表层沉积物中的浓度范围为 33718ngkg(-1)。所有样本均表现出 OCDD 异常高浓度和极低比例的 PCDFs。不同的电子废物回收程序可能会产生不同的同系物分布。在这种情况下,露天焚烧和拆解是两种排放较高浓度 PCDD/Fs 的程序,这表明低技术回收作业是 PCDD/Fs 向环境排放的主要来源之一。不同环境基质中浓度和同系物/同类物分布的变化和区别,揭示了污染物在从“源”到“汇”的迁移过程中的环境行为和归宿特征。通过土壤摄入和皮肤吸收摄入 PCDD/Fs 的量可以忽略不计,但估计的总 PCDD/F 摄入剂量远远超过了世界卫生组织建议的 4pg-TEQ/kg/d 的耐受日摄入量值,这表明龙塘居民面临着接触二恶英的高风险,尤其是儿童。

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