首页> 外文期刊>Analytical chemistry >Chemometrics-Assisted Excitation-Emission Fluorescence Spectroscopy on Nylon Membranes. Simultaneous Determination of Benzo[a]pyrene and Dibenz[a,h]anthracene at Parts-Per-Trillion Levels in the Presence of the Remaining EPA PAH Priority...
【24h】

Chemometrics-Assisted Excitation-Emission Fluorescence Spectroscopy on Nylon Membranes. Simultaneous Determination of Benzo[a]pyrene and Dibenz[a,h]anthracene at Parts-Per-Trillion Levels in the Presence of the Remaining EPA PAH Priority...

机译:尼龙膜的化学计量学激发-发射荧光光谱法。在剩余的EPA PAH优先存在的情况下,同时以每万亿分之几的含量同时测定苯并[a​​] re和Dibenz [a,h]蒽

获取原文
获取原文并翻译 | 示例
       

摘要

This work presents a novel approach for the simultaneous ultratrace determination of benzo[a]pyrene and dibenzo[a,h]anthracene, the two most carcinogenic polycyclic aromatic hydrocarbons (PAHs), in a very interfering environment, combining the recently discovered ability of the nylon membrane to strongly retain and concentrate PAHs on its surface, the sensitivity of molecular fluorescence, and the selectivity of second-order chemometric algorithms. The fluorescence excitation-emission matrices, directly measured on a nylon-membrane surface, are processed by applying parallel factor analysis (PARAFAC) and unfolded partial least-squares coupled to residual bilinearization (U-PLS/RBL). The superiority of U-PLS/RBL to quantify BaP and DBA at concentrations below 10 ng L~(-1) in the presence of the remaining 14 US EPA (United States Environmental Protection Agency) PAHs at total concentrations ranging from 1400 and 14 000 ng L~(-1) is demonstrated. The present method successfully faces this complex challenge without using organic solvents, which are to known produce environmental contamination. Finally, the high sensitivity of the present method avoids preconcentration and elution steps, considerably decreasing the analysis time and the experimental errors. Because the instrumental involved in the determination is nonsophisticated, the experiments could be carried out in routine laboratories.
机译:这项工作提出了一种在极强干扰性的环境中同时超痕量测定两种致癌性最高的多环芳烃(PAHs)苯并[a] py和二苯并[a,h]蒽的新方法,结合了最近发现的尼龙膜可将PAHs强力保留并浓缩在其表面上,分子荧光的敏感性以及二阶化学计量学算法的选择性。通过应用平行因子分析(PARAFAC)和未折叠的部分最小二乘法与残留双线性化(U-PLS / RBL)耦合,可以直接在尼龙膜表面上测量荧光激发-发射矩阵。在剩余的14种美国EPA(美国环境保护署)PAH的存在下,U-PLS / RBL在低于10 ng L〜(-1)的浓度下定量BaP和DBA的优越性,总浓度在1400和14 000之间ng L〜(-1)被证明。本方法在不使用已知会造成环境污染的有机溶剂的情况下成功地克服了这一复杂的挑战。最后,本方法的高灵敏度避免了预浓缩和洗脱步骤,大大减少了分析时间和实验误差。由于确定过程中涉及的工具并不复杂,因此可以在常规实验室中进行实验。

著录项

相似文献

  • 外文文献
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