首页> 外文期刊>Analytical Chemistry >DETERMINATION OF NANOGRAM PER LITER CONCENTRATIONS OF VOLATILE ORGANIC COMPOUNDS IN WATER BY CAPILLARY GAS CHROMATOGRAPHY AND SELECTED ION MONITORING MASS SPECTROMETRY AND ITS USE TO DEFINE GROUNDWATER FLOW DIRECTIONS IN EDWARDS AQUIFER, TEXAS
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DETERMINATION OF NANOGRAM PER LITER CONCENTRATIONS OF VOLATILE ORGANIC COMPOUNDS IN WATER BY CAPILLARY GAS CHROMATOGRAPHY AND SELECTED ION MONITORING MASS SPECTROMETRY AND ITS USE TO DEFINE GROUNDWATER FLOW DIRECTIONS IN EDWARDS AQUIFER, TEXAS

机译:毛细管气相色谱法和离子选择性质谱法测定水中挥发性有机化合物的毫微克浓度

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摘要

method has been developed to measure nanogram per liter amounts of selected volatile organic compounds (VOCs) including dichlorodifluoromethane, trichlorofluoromethane, cis-1,2-dichloroethene, trichloroethene, tetrachloroethene, and the isomers of dichlorobenzene in water. The method uses purge-and-trap techniques on a 100 mL sample, gas chromatography with a megabore capillary column, and electron impact, selected ion monitoring mass spectrometry. Minimum detection levels for these compounds ranged from 1 to 4 ng/L in water. Recoveries from organic-free distilled water and natural groundwater ranged from 70.5% for dichlorodifluoromethane to 107.8% for 1,4-dichlorobenzene. Precision was generally best for cis-1,2-dichloroethene, tetrachloroethene, and the dichlorobenzene isomers and worst for dichlorodifluoromethane and trichlorofluoromethane. Blank data indicated persistent, trace-level introduction of dichlorodifluoromethane, 1,4-dichlorobenzene and tetrachloroethene to samples during storage and shipment at concentrations less than the method reporting limits. The largest concentrations of the selected VOCs in 27 water samples from the Edwards aquifer near San Antonio, TX, were from contined-zone wells near an abandoned landfill. The results defined a zone of water with no detectable VOCs in nearly all of the aquifer west of San Antonio and from part of the confined zone beneath San Antonio.
机译:已开发出一种方法来测量每升选定的挥发性有机化合物(VOC)纳克,包括二氯二氟甲烷,三氯氟甲烷,顺式1,2-二氯乙烯,三氯乙烯,四氯乙烯和水中的二氯苯异构体。该方法使用100 mL样品的吹扫捕集技术,带有大口径毛细管柱的气相色谱法和电子碰撞技术,以及选定的离子监测质谱仪。这些化合物在水中的最低检测水平为1-4 ng / L。从不含有机物的蒸馏水和天然地下水中的回收率范围从二氯二氟甲烷的70.5%到1,4-二氯苯的107.8%。对于顺式1,2-二氯乙烯,四氯乙烯和二氯苯异构体,精度通常最好,而对二氯二氟甲烷和三氯氟甲烷则最差。空白数据表明在储存和运输期间,样品中的二氯二氟甲烷,1,4-二氯苯和四氯乙烯持续微量地引入,其浓度低于方法报告的极限。在得克萨斯州圣安东尼奥市附近的爱德华兹含水层的27个水样中,所选择的VOC的最大浓度来自一个废弃填埋场附近的连续带井。结果确定了圣安东尼奥以西几乎所有含水层以及圣安东尼奥下方的部分受限区域中没有可检测到的VOC的水域。

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  • 来源
    《Analytical Chemistry》 |1995年第20期|p.3659-3667|共9页
  • 作者单位

    Buszka PM, US GEOL SURVEY, 5957 LAKESIDE BLVD, INDIANAPOLIS, IN 46278, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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