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SPATIALLY RESOLVED TIME-OF-FLIGHT MASS SPECTROMETRY OF POLYCYCLIC AROMATIC HYDROCARBONS - QUANTIFICATION STUDIES

机译:多分辨芳烃的飞行时间质谱解析-定量研究

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摘要

Deuterated polycyclic aromatic hydrocarbons (PAHs) have been employed as surrogate internal standards for the quantitative analysis of PAHs by laser postionization time-of-flight mass spectrometry, Experiments were performed on intimate mixtures of chrysene and chrysene-d(12) which were desorbed from thin films at 266 nm using a tightly focused (1-2 mu m) Nd-YAG laser beam. The neutral molecules within the laser-desorbed plume were ionized by a frequency-doubled dye laser at 260 nn. Under soft ionization conditions, the mass spectrum comprised peaks associated with the parent ion envelope with negligible amounts of fragment ions at lower masses. The ratio of the peak areas of the parent ions of chrysene and chrysene-d(12) was proportional to their relative molar concentrations in the standard solutions, With the use of chrysene-d(12) as an internal standard, the determined concentration of chrysene in an NIST standard was in good agreement with the certified value.
机译:氘代多环芳烃(PAHs)已被用作替代内标,用于通过激光后离子化飞行时间质谱法对PAHs进行定量分析,并进行了从中脱附的chrysene和chrysene-d(12)的紧密混合物的实验。使用紧密聚焦(1-2微米)的Nd-YAG激光束在266 nm处形成薄膜。激光解吸羽流中的中性分子被倍频的染料激光在260 nn电离。在软电离条件下,质谱图包含与母体离子包络线相关的峰,较低质量的碎片离子量可忽略不计。 the和solutions-d(12)母体离子的峰面积之比与标准溶液中它们的相对摩尔浓度成正比。使用-d(12)作为内标,确定的浓度NIST标准中的chrysene与认证值非常吻合。

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