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比较在线耦合高效液相色谱-气相色谱-火焰离子化检测法中分离和定量矿物油烃(MOH)馏分所用载气。

Comparison of carrier gases for the separation and quantification of mineral oil hydrocarbon (MOH) fractions using online coupled high performance liquid chromatography-gas chromatography-flame ionisation detection.

机构信息

Axel Semrau GmbH, Stefansbecke 42, 45549 Sprockhövel, Germany; Bundesanstalt für Materialforschung und -prüfung (BAM), Unter den Eichen 87, 12205 Berlin, Germany.

Bundesanstalt für Materialforschung und -prüfung (BAM), Unter den Eichen 87, 12205 Berlin, Germany.

出版信息

J Chromatogr A. 2024 Jul 5;1726:464946. doi: 10.1016/j.chroma.2024.464946. Epub 2024 Apr 28.

DOI:10.1016/j.chroma.2024.464946
PMID:38744185
Abstract

On-line coupled high performance liquid chromatography-gas chromatography-flame ionisation detection (HPLC-GC-FID) was used to compare the effect of hydrogen, helium and nitrogen as carrier gases on the chromatographic characteristics for the quantification of mineral oil hydrocarbon (MOH) traces in food related matrices. After optimisation of chromatographic parameters nitrogen carrier gas exhibited characteristics equivalent to hydrogen and helium regarding requirements set by current guidelines and standardisation such as linear range, quantification limit and carry over. Though nitrogen expectedly led to greater peak widths, all required separations of standard compounds were sufficient and humps of saturated mineral oil hydrocarbons (MOSH) and aromatic mineral oil hydrocarbons (MOAH) were appropriate to enable quantitation similar to situations where hydrogen or helium had been used. Slightly increased peak widths of individual hump components did not affect shapes and widths of the MOSH and MOAH humps were not significantly affected by the use of nitrogen as carrier gas. Notably, nitrogen carrier gas led to less solvent peak tailing and smaller baseline offset. Overall, nitrogen may be regarded as viable alternative to hydrogen or helium and may even extend the range of quantifiable compounds to highly volatile hydrocarbon eluting directly after the solvent peak.

摘要

在线耦合高效液相色谱-气相色谱-火焰离子化检测(HPLC-GC-FID)被用于比较氢气、氦气和氮气作为载气对食品相关基质中矿物油烃(MOH)痕量定量的色谱特征的影响。在优化了色谱参数后,氮气载气在现行指南和标准化所规定的线性范围、定量限和残留等要求方面表现出与氢气和氦气相当的特征。尽管氮气预计会导致更大的峰宽,但所有标准化合物的所需分离都足够充分,饱和矿物油烃(MOSH)和芳香族矿物油烃(MOAH)的峰肩也足以进行定量,类似于使用氢气或氦气的情况。个别峰肩成分的略微增加的峰宽不会影响 MOSH 和 MOAH 峰肩的形状和宽度,氮气作为载气的使用也没有对其产生显著影响。值得注意的是,氮气载气导致的溶剂峰拖尾较少,基线偏移较小。总体而言,氮气可以被视为氢气或氦气的可行替代品,甚至可以将可定量化合物的范围扩展到直接在溶剂峰后洗脱的高挥发性烃类。

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