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《阿格博格布洛西电子废物场(加纳)土壤中溴化/氯化二苯醚和二苯并呋喃的复杂混合物:出现、形成及暴露影响》

Complex Mixtures of Brominated/Chlorinated Diphenyl Ethers and Dibenzofurans in Soils from the Agbogbloshie e-Waste Site (Ghana): Occurrence, Formation, and Exposure Implications.

机构信息

Center for Marine Environmental Studies (CMES) , Ehime University , 2-5 Bunkyo-cho , Matsuyama 790-8577 , Japan.

CSIR Water Research Institute , P.O. Box AH 38, Achimota, Accra , Ghana.

出版信息

Environ Sci Technol. 2019 Mar 19;53(6):3010-3017. doi: 10.1021/acs.est.8b06929. Epub 2019 Mar 1.

Abstract

The distribution and toxic equivalents (TEQs) of brominated and chlorinated dibenzo- p-dioxins/dibenzofurans (PBDD/Fs and PCDD/Fs) in soils from Agbogbloshie e-waste site (Ghana) were investigated. The composition of brominated/chlorinated dibenzofurans (PXDFs) and diphenyl ethers (PBDEs, PCDEs, and PXDEs) was examined using two-dimensional gas chromatography-time-of-flight mass spectrometry to elucidate possible formation pathways of dioxins from e-waste recycling. The highest concentrations of PCDD/Fs and PBDD/Fs were found, respectively, in the open burning (1.3-380 ng/g dry weight) and dismantling areas (11-1000 ng/g dry weight) and were comparable to the highest reported for informal e-waste sites. PXDFs and PXDEs were detected at up to the range of hundreds of nanograms per gram. The homologue profiles suggest that PXDFs were formed mainly from PBDFs through successive Br-to-Cl exchange. However, monobromo-PCDFs were also derived from de-novo-generated PCDFs in open burning areas. PBDFs contributed similar or higher TEQs (7.9-5400 pg/g dry weight) compared with PCDD/Fs (6.8-5200 pg/g dry weight), whereas PXDFs were also substantial TEQ contributors in open burning areas. The high TEQs of PBDFs in the dismantling area (120-5200 pg/g dry weight) indicate the need to consider brominated dioxins besides chlorinated dioxins in future studies on health implications for e-waste workers and local residents.

摘要

研究了阿格博格布洛西电子垃圾场(加纳)土壤中溴化和氯化二苯并-对-二恶英/呋喃(PBDD/Fs 和 PCDD/Fs)的分布和毒性当量(TEQs)。使用二维气相色谱-飞行时间质谱法研究了溴化/氯化二苯并呋喃(PXDFs)和二苯醚(PBDEs、PCDEs 和 PXDEs)的组成,以阐明电子废物回收中二恶英的可能形成途径。在露天焚烧(1.3-380ng/g 干重)和拆解区(11-1000ng/g 干重)发现了最高浓度的 PCDD/Fs 和 PBDD/Fs,与非正规电子废物场的最高报告值相当。检测到高达数百纳克/克的 PXDFs 和 PXDEs。同系物分布表明,PXDFs 主要通过 Br 到 Cl 的连续交换从 PBDFs 形成。然而,在露天焚烧区,单溴-PCDFs 也来自新生成的 PCDFs。与 PCDD/Fs(6.8-5200pg/g 干重)相比,PBDFs 对 TEQs 的贡献相似或更高(7.9-5400pg/g 干重),而在露天焚烧区,PXDFs 也是重要的 TEQ 贡献者。在拆解区(120-5200pg/g 干重),PBDFs 的高 TEQs 表明,在未来关于电子废物工人和当地居民健康影响的研究中,需要考虑除氯化二恶英以外的溴化二恶英。

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