...
首页> 外文期刊>Analytical chemistry >Direct determination of soil surface bound polycyclic aromatic hydrocarbons in petroleum-contaminated soils by real time aerosol mass spectrometry
【24h】

Direct determination of soil surface bound polycyclic aromatic hydrocarbons in petroleum-contaminated soils by real time aerosol mass spectrometry

机译:实时气溶胶质谱法直接测定石油污染土壤中土壤表面结合的多环芳烃

获取原文
获取原文并翻译 | 示例

摘要

Soil surface-bound polycyclic aromatic hydrocarbons (PAHs) were identified by use of Real-Tune Aerosol Mass Spectrometry (RTAMS) in two NIST standard research material (SRM) soils (Montana SRM 2710 and Peruvian SRM 4355) each contaminated separately with three common petroleum hydrocarbons (diesel fuel, gasoline, and kerosene). The described contaminated soil analysis required no sample preparation. Direct laser desorption/ionization mass spectrometric analysis of individual soil particles contaminated with each of the petroleum hydro-carbons at three different contamination levels (0.8, 8, and 80 ppth (wt/wt)) yielded detectable PAH cation distributions that ranged from m/z 128 to 234, depending on the fuel contaminant. The same analysis performed on uncontaminated SRM soils revealed very little (Peruvian) to no (Montana) detectable PAH species. Size analysis showed that most of the individual soil particles analyzed were between 1 and 5 pm in diameter. Tandem mass spectrometry (MS/MS) experiments identified alkyl-substituted two- and three-ringed PAHs in all three petroleum hydrocarbon contaminated soils. However, due to similarities in fragmentation patterns, MS/MS analysis of higher MW species (m/z > 200) was unable to distinguish between the possibility of highly alkyl-substituted three-ringed PAHs and hydrogenated four-ringed PAHs, The described technique offers the direct, rapid determination and characterization of surface-bound PAHs in petroleum-contaminated soils at part-per-million levels without prior extraction, separation, or other sample preparation methods. [References: 55]
机译:通过使用Real-Tune气溶胶质谱法(RTAMS)在两种NIST标准研究材料(SRM)土壤(蒙大拿州SRM 2710和秘鲁SRM 4355)中分别识别土壤表面结合的多环芳烃(PAHs),每种土壤分别被三种普通石油污染碳氢化合物(柴油,汽油和煤油)。所描述的受污染土壤分析不需要样品制备。直接激光解吸/电离质谱分析在三种不同污染水平(0.8、8和80 ppth(wt / wt))下被每种石油烃污染的单个土壤颗粒,产生可检测的PAH阳离子分布,范围为m / z 128至234,取决于燃油污染物。在未污染的SRM土壤上进行的相同分析显示,很少(秘鲁)到没有(蒙大拿州)可检测到的PAH物种。尺寸分析表明,所分析的大多数单个土壤颗粒的直径在1-5 pm之间。串联质谱(MS / MS)实验在所有三种石油烃污染的土壤中鉴定出烷基取代的二环和三环PAH。但是,由于片段化模式的相似性,较高分子量物种(m / z> 200)的MS / MS分析无法区分高度烷基取代的三环PAH和氢化的四环PAH的可能性。无需事先提取,分离或其他样品前处理方法,即可直接,快速测定和表征石油污染土壤中表面结合的PAH(百万分之一)。 [参考:55]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号