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巴黎地区(法国)农业和非农用地中邻苯二甲酸酯和双酚 A 的归宿。

Fate of phthalates and BPA in agricultural and non-agricultural soils of the Paris area (France).

机构信息

EPHE, UMR 7619 METIS, UPMC - Univ Paris 06 / CNRS / EPHE, 4 place Jussieu, 75005, Paris, France.

出版信息

Environ Sci Pollut Res Int. 2015 Jul;22(14):11118-26. doi: 10.1007/s11356-015-4178-3. Epub 2015 Mar 22.

DOI:10.1007/s11356-015-4178-3
PMID:25794574
Abstract

This study (i) investigated the concentration levels of nine phthalates and bisphenol A (BPA) in sludge samples originating from a French wastewater treatment plant (WWTP), (ii) studied the distribution of target compounds according to soil depth and calculated their half-lives, and (iii) compared the contamination level of the agricultural soil with those of soils with other land uses. The sludge contamination levels varied from a few hundred nanograms per gram dry weight (dw) for diethyl phthalate (DEP), di-iso-butyl phthalate (DiBP), di-n-butyl phthalate (DnBP), and butyl-benzyl phthalate (BBP) to a few micrograms per gram dw for diethylhexyl phthalate (DEHP), di-iso-nonyl phthalate (DiNP), and di-iso-decyl phthalate (DiDP). After sludge application, an 8-fold increase for DEHP level and a 3-fold increase for BPA level occurred in the surface horizon of the soil. The mean distribution of phthalates according to the depth showed a positive gradient for the low molecular weight compounds and inversely, a negative gradient for the highest ones. The half-lives in the 0-20-cm soil horizon were 64 days for DEHP and 36 days for BPA. A predictive environmental concentration (PEC) of 0.3 μg g(-1) dw was estimated for DEHP, while the experimental value was 0.16 μg g(-1) dw, suggesting degradation processes in soil and/or formation of non-extractable residues. Comparisons of contamination levels for soils from different origins (urban, rural, agricultural, and forest) showed that the urban soil remained the most contaminated one, prior to the agricultural soil after treatment.

摘要

本研究

(i) 调查了来自法国污水处理厂(WWTP)的污泥样本中 9 种邻苯二甲酸酯和双酚 A(BPA)的浓度水平;(ii) 研究了目标化合物在土壤深度上的分布,并计算了它们的半衰期;(iii) 比较了农业土壤的污染水平与其他土地利用土壤的污染水平。污泥的污染水平从几百纳克/克干重(dw)的邻苯二甲酸二乙酯(DEP)、邻苯二甲酸二异丁酯(DiBP)、邻苯二甲酸二正丁酯(DnBP)和邻苯二甲酸丁基苄基酯(BBP)到几微克/克 dw 的邻苯二甲酸二(2-乙基己基)酯(DEHP)、邻苯二甲酸二异壬酯(DiNP)和邻苯二甲酸二异癸酯(DiDP)不等。在污泥施用后,土壤表层中 DEHP 水平增加了 8 倍,BPA 水平增加了 3 倍。根据深度对邻苯二甲酸酯的平均分布显示,低分子量化合物呈正梯度,而最高分子量化合物呈负梯度。0-20cm 土壤层中的半衰期分别为 DEHP 的 64 天和 BPA 的 36 天。DEHP 的预测环境浓度(PEC)为 0.3μg g(-1) dw,而实验值为 0.16μg g(-1) dw,表明土壤中存在降解过程和/或形成不可提取的残留物。不同来源(城市、农村、农业和森林)土壤的污染水平比较表明,在处理前,城市土壤仍然是污染最严重的土壤,其次是农业土壤。

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