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尼日利亚电子废物拆解和倾倒场土壤和室外灰尘中有机磷阻燃剂和增塑剂的来源识别和人体暴露评估。

Source identification and human exposure assessment of organophosphate flame retardants and plasticisers in soil and outdoor dust from Nigerian e-waste dismantling and dumpsites.

机构信息

Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610, Wilrijk, Belgium; Department of Chemistry, University of Lagos, Lagos State, Nigeria; Chemistry Department, Chrisland University, Ogun State, 23409, Nigeria.

Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610, Wilrijk, Belgium.

出版信息

Environ Pollut. 2024 Dec 1;362:124998. doi: 10.1016/j.envpol.2024.124998. Epub 2024 Sep 21.

Abstract

Electronic waste (e-waste) dismantling and dumpsite processes are major sources of organophosphate flame retardant and plasticiser emissions and may pose potentially adverse effects on environment and human health. In 20 outdoor dust and 49 soil samples collected from four e-waste dismantling and three e-waste dumpsites in two States of Nigeria (Lagos and Ogun), we identified 13 alternative plasticisers (APs), 7 legacy phthalate plasticisers (LPs), and 17 organophosphorus flame retardants (OPFRs) for the first time in African e-waste streams. In the samples from dismantling sites, the range (median) concentrations of ∑APs, ∑LPs, and ∑OPFRs were 11-2747 μg/g (144 μg/g), 11-396 μg/g (125 μg/g), and 0.2-68 μg/g (5.5 μg), in dust respectively and 1.8-297 μg/g (55 μg/g), 1.3-274 μg/g (48.5 μg/g), and 1.6-62 μg/g (1.6 μg/g), in soil respectively. Results for soil samples from e-waste dumpsites were (6.6-195 μg/g (23.7 μg/g), 6.0-295 μg/g (54.8), and 0.4-42.3 μg/g (9.0 μg/g) for ∑APs, ∑LPs, and ∑OPFRs respectively. Overall, concentrations of APs were significantly higher at the dismantling sites (p = 0.005) compared to dumpsites, levels of LPs were higher at dismantling sites but not significant, while OPFR concentrations were significantly higher in dumpsite samples (p = 0.005). Plasticisers were found to be major contributors to pollution at e-waste dismantling sites, while OPFRs were associated with both automobile dismantling and e-waste dumpsite processes. Following particle size fractionation of selected soil samples, higher concentrations of targeted compounds were observed in the smaller mesh (180 μm) soil sieve fraction. For dust, the total median estimated daily intake via ingestion and dermal adsorption (EDI and EDI) ranged from 43 to 74 ng/kg bw/day and 0.4-0.7 ng/kg bw/day, respectively. Correspondingly, 4.6-45 ng/kg bw/day and 0.015-0.57 ng/kg bw/day were the values found for soil, respectively. According to these results, the targeted chemicals do not appear to pose a non-carcinogenic risk to e-waste workers through ingestion or dermal contact of bio-accessible fractions of the chemicals. Human biomonitoring campaigns are recommended in the Nigerian e-waste environment considering the elevated concentration levels found for the majority of targeted compounds and that risk parameters required for exposure assessment were only available for a limited number of compounds.

摘要

电子废物(e-waste)拆解和垃圾场过程是有机磷阻燃剂和增塑剂排放的主要来源,可能对环境和人类健康造成潜在的不利影响。在尼日利亚两个州(拉各斯和奥贡)的四个电子废物拆解场和三个电子废物垃圾场收集的 20 个室外灰尘和 49 个土壤样本中,我们首次在非洲电子废物中确定了 13 种替代增塑剂(APs)、7 种传统邻苯二甲酸酯增塑剂(LPs)和 17 种有机磷阻燃剂(OPFRs)。在拆解场的样本中,∑APs、∑LPs 和∑OPFRs 的浓度范围(中位数)分别为 11-2747μg/g(144μg/g)、11-396μg/g(125μg/g)和 0.2-68μg/g(5.5μg/g),在灰尘中;1.8-297μg/g(55μg/g)、1.3-274μg/g(48.5μg/g)和 1.6-62μg/g(1.6μg/g),在土壤中。电子废物垃圾场土壤样本的结果分别为(6.6-195μg/g(23.7μg/g)、6.0-295μg/g(54.8μg/g)和 0.4-42.3μg/g(9.0μg/g)。总体而言,与垃圾场相比,APs 在拆解场的浓度显著更高(p=0.005),LPs 在拆解场的浓度更高但无统计学意义,而 OPFRs 的浓度在垃圾场样本中显著更高(p=0.005)。研究发现,增塑剂是电子废物拆解场污染的主要贡献者,而 OPFRs 与汽车拆解和电子废物垃圾场过程有关。对选定土壤样本进行颗粒大小分级后,发现较小筛网(180μm)土壤筛部分的目标化合物浓度更高。对于灰尘,通过摄入和皮肤吸附(EDI 和 EDI)估计的每日总摄入量中位数范围分别为 43 至 74ng/kg bw/天和 0.4-0.7ng/kg bw/天。相应地,土壤中的值分别为 4.6-45ng/kg bw/天和 0.015-0.57ng/kg bw/天。根据这些结果,通过摄入或皮肤接触可接触部分的化学品,目标化学品似乎不会对电子废物工人造成非致癌风险。鉴于大多数目标化合物的浓度较高,并且仅对有限数量的化合物获得了进行暴露评估所需的风险参数,因此建议在尼日利亚电子废物环境中开展人体生物监测活动。

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