首页> 外文期刊>The Science of the Total Environment >Spatial distributions and transport implications of short- and medium-chain chlorinated paraffins in soils and sediments from an e-waste dismantling area in China
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Spatial distributions and transport implications of short- and medium-chain chlorinated paraffins in soils and sediments from an e-waste dismantling area in China

机译:中国电子废物拆解区土壤和沉积物中短链和中链氯化石蜡的空间分布和运输意义

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To investigate the spatial distributions, potential transport and ecological risks of chlorinated paraffins (CPs) in and around e-waste dismantling area, we collected soil samples within 5 km of the e-waste dismantling centers and sediment samples in the surrounding area from the lower reaches of Jiaojiang River. Short- and medium-chain chlorinated paraffins (SCCPs and MCCPs) were analyzed by two-dimensional gas chromatography coupled with electron-capture negative-ionization mass spectrometry (GC x GC-ECNI-MS). The SCCP and MCCP concentration ranges in soils were 68.5 to 2.20 x 10(5) ng/g dry weight (dw) and 507 to 4.40 x 10(6) ng/g dw, respectively. The ranges for the levels of SCCPs and MCCPs in sediments were 32.5-1.29 x 10(4) ng/g dw and 271-2.72 x 10(4) ng/g dw, respectively. No significant correlation was observed between total organic carbon (TOC) and CP concentrations (P 0.05). The spatial distributions showed that the CP levels were closely related to e-waste pollution. Correspondence analysis revealed that shorter-chain and less chlorinated congeners were enriched in sediments from sites distant from e-waste pollution source, while longer-chain and higher chlorinated congeners were concentrated in soils and sediments collected near the pollution source, which indicated that complex environmental processes, such as transportation via atmosphere and/or water, and deposition, resulted in different CP profiles in different sampling locations and environment matrixes (e.g., soil and sediments). Principal component analysis (PCA) indicated that e-waste pollution could be the same source of SCCPs and MCCPs. The preliminary risk assessment indicated that CPs in soils within 1 km of e-waste dismantling centers at current levels posed a considerable risk to soil-dwelling organisms, and the sediment MCCPs in Jiaojiang estuary at present levels also posed a risk to sediment-dwelling organisms. (C) 2018 Elsevier B.V. All rights reserved.
机译:为了调查电子废物拆解区内和周围的氯化石蜡(CP)的空间分布,潜在的运输和生态风险,我们收集了电子废物拆解中心5公里以内的土壤样本,并从下部收集了周围地区的沉积物样本。椒江。短链和中链氯化石蜡(SCCP和MCCP)通过二维气相色谱与电子捕获负电离质谱(GC x GC-ECNI-MS)结合进行分析。土壤中的SCCP和MCCP浓度范围分别为68.5至2.20 x 10(5)ng / g干重(dw)和507至4.40 x 10(6)ng / g dw。沉积物中短链氯化石蜡和多氯联苯的含量范围分别为32.5-1.29 x 10(4)ng / g dw和271-2.72 x 10(4)ng / g dw。总有机碳(TOC)与CP浓度之间没有显着相关性(P> 0.05)。空间分布表明,CP水平与电子废物污染密切相关。对应分析表明,短链低氯同类物富集在远离电子废物污染源的地点的沉积物中,而长链高氯同类物则集中在污染源附近的土壤和沉积物中,这表明环境复杂。过程,例如通过大气和/或水的运输以及沉积,在不同的采样位置和环境矩阵(例如,土壤和沉积物)中产生了不同的CP轮廓。主成分分析(PCA)表明,电子废物污染可能是短链氯化石蜡和多氯联苯CPCC的同一来源。初步风险评估表明,目前水平的电子废物拆解中心1公里以内的土壤中的CPs对居住在土壤中的生物构成了相当大的风险,而目前椒江河口的沉积物MCCP对居住在地下的生物也构成了风险。 。 (C)2018 Elsevier B.V.保留所有权利。

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