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沿海环境沉积物中超痕量咔唑的定量测定。

Quantitative determination of ultra-trace carbazoles in sediments in the coastal environment.

作者信息

Chen Wen-Ling, Xie Zhiyong, Wolschke Hendrik, Gandrass Juergen, Kötke Danijela, Winkelmann Magnus, Ebinghaus Ralf

机构信息

Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, Institute of Coastal Research, Department for Environmental Chemistry, Geesthacht 21502, Germany.

出版信息

Chemosphere. 2016 May;150:586-595. doi: 10.1016/j.chemosphere.2016.02.051. Epub 2016 Feb 24.

Abstract

Carbazole and some of its derivatives may possess dioxin-like toxicity and could be persistent in the environment, but information on their distribution and environmental fate is limited. This study developed and validated an ultra-trace targeted-analysis method for the determination of carbazole, 1,2-benzocarbazole, and 13 halogenated carbazoles in sediments from the river, coast, and North Sea. An 8-g sediment sample was extracted using accelerated solvent extraction combined with in-cell cleanup and analyzed using gas chromatography-tandem mass spectrometry. The method was sensitive and reliable with method detection limits ranging from 4.54 to 52.9 pg/g, and most of the quantification biases and relative standard deviations were <20 and <15%, respectively. Carbazole and 1,2-benzocarbazole were the predominant substances in the sediments (median 565 and 369 pg/g, respectively) followed by 3,6-dichlorocarbazole (median 196 pg/g). The detection frequencies of carbazole, benzo-, 3-chloro-, and 3,6-dichlorocarbazole were >75%, while those of 3,6-dibromo-, 1-bromo-3,6-dichloro-, and 1,8-dibromo-3,6-dichlorocarbazole were approximately 50%. Brominated carbazoles occurred more frequently in marine than river-influenced sediments, which could indicate halogenation after discharge into the river. This is the first study regarding these substances in coastal environments without apparent contamination history. The ubiquity and bioaccumulative potential of these substances needs to be considered.

摘要

咔唑及其一些衍生物可能具有二噁英样毒性,并且可能在环境中持久存在,但关于它们的分布和环境归宿的信息有限。本研究开发并验证了一种超痕量靶向分析方法,用于测定河流、海岸和北海沉积物中的咔唑、1,2-苯并咔唑和13种卤代咔唑。采用加速溶剂萃取结合柱内净化法提取8 g沉积物样品,并使用气相色谱-串联质谱法进行分析。该方法灵敏可靠,方法检出限为4.54至52.9 pg/g,大多数定量偏差和相对标准偏差分别<20%和<15%。咔唑和1,2-苯并咔唑是沉积物中的主要物质(中位数分别为565和369 pg/g),其次是3,6-二氯咔唑(中位数为196 pg/g)。咔唑、苯并咔唑、3-氯咔唑和3,6-二氯咔唑的检出频率>75%,而3,6-二溴咔唑、1-溴-3,6-二氯咔唑和1,8-二溴-3,6-二氯咔唑的检出频率约为50%。溴代咔唑在海洋沉积物中比受河流影响的沉积物中出现得更频繁,这可能表明其排放到河流后发生了卤化作用。这是关于这些物质在没有明显污染历史的沿海环境中的首次研究。需要考虑这些物质的普遍性和生物累积潜力。

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