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摆线电子单色仪/质谱仪系统在环境化学物质研究中的应用。

Application of a trochoidal electron monochromator/mass spectrometer system to the study of environmental chemicals.

作者信息

Laramée J A, Kocher C A, Deinzer M L

机构信息

Department of Agricultural Chemistry, Oregon State University, Corvallis 97331.

出版信息

Anal Chem. 1992 Oct 15;64(20):2316-22. doi: 10.1021/ac00044a003.

Abstract

A trochoidal electron monochromator has been interfaced to a mass spectrometer to perform electron capture negative ion mass spectrometric (ECNIMS) analyses of environmentally relevant chemicals. The kinetic energy of the electron beam can be varied from 0.025 to 30 eV under computer control. No reagent gas is used to moderate the electron energies. An electron energy spread of +/- 0.1 to +/- 0.4 eV full width at half-maximum (fwhm) can readily be obtained at a transmitted current of 2 x 10(-6) A, improving to +/- 0.07 eV at 5 x 10(-7) A. Comparisons of ECNI results from the electron monochromator/mass spectrometer system with those from a standard instrument that uses a moderating gas show similar spectra for heptachlor but not for the s-triazine herbicides, as for example, atrazine. This compound shows numerous adduct ions by standard ECNIMS that are eliminated by using the electron monochromator to generate the mass spectra. Isomeric tetrachlorodibenzo-p-dioxins show distinct differences in the electron energies needed to produce the maximum amount of parent and fragment anions. Multiple resonance states resulting in stable radical anions (M.-) are easily observed for nitrobenzene and for polycyclic aromatic hydrocarbons. Ionic products of dissociative electron capture invariably occur from several resonance states.

摘要

一台摆线电子单色仪已与一台质谱仪连接,用于对环境相关化学品进行电子捕获负离子质谱(ECNIMS)分析。在计算机控制下,电子束的动能可在0.025至30电子伏特之间变化。不使用反应气来调节电子能量。在2×10⁻⁶安的传输电流下,半高宽(fwhm)为±0.1至±0.4电子伏特的电子能量分散很容易获得,在5×10⁻⁷安时可提高到±0.07电子伏特。将电子单色仪/质谱仪系统的ECNI结果与使用缓和气体的标准仪器的结果进行比较,对于七氯显示出相似的光谱,但对于s - 三嗪除草剂,如阿特拉津则不然。该化合物通过标准ECNIMS显示出许多加合离子,而使用电子单色仪生成质谱时这些加合离子会被消除。异构四氯二苯并 - p - 二恶英在产生最大量的母体和碎片阴离子所需的电子能量方面表现出明显差异。对于硝基苯和多环芳烃,很容易观察到导致稳定自由基阴离子(M⁻)的多重共振态。离解电子捕获的离子产物总是从几个共振态产生。

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