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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Ultrasonication extraction and gel permeation chromatography clean-up for the determination of polycyclic aromatic hydrocarbons in edible oil by an isotope dilution gas chromatography-mass spectrometry
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Ultrasonication extraction and gel permeation chromatography clean-up for the determination of polycyclic aromatic hydrocarbons in edible oil by an isotope dilution gas chromatography-mass spectrometry

机译:超声稀释-凝胶渗透色谱净化-同位素稀释气相色谱-质谱法测定食用油中的多环芳烃

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摘要

An analytical method for the determination of US EPA priority pollutant 16 polycyclic aromatic hydrocarbons (PAHs) in edible oil was developed by an isotope dilution gas chromatography-mass spectrometry (GC-MS). Extraction was performed with ultrasonication mode using acetonitrile as solvent, and subsequent clean-up was applied using narrow gel permeation chromatographic column. Three deuterated PAHs surrogate standards were used as internal standards for quantification and analytical quality control. The limits of quantification (LOQs) were globally below 0.5. ng/g, the recoveries were in the range of 81-96%, and the relative standard deviations (RSDs) were lower than 20%. Further trueness assessment of the method was also verified through participation in international cocoa butter proficiency test (T0638) organised by the FAPAS with excellent results in 2008. The results obtained with the described method were satisfying (z≤2). The method has been applied to determine PAH in real edible oil samples.
机译:通过同位素稀释气相色谱-质谱法(GC-MS)建立了一种测定食用油中美国EPA优先污染物16种多环芳烃(PAHs)的分析方法。以乙腈为溶剂,以超声模式进行萃取,然后使用窄凝胶渗透色谱柱进行后续纯化。三种氘化的PAHs替代标准品用作定量和分析质量控制的内标。定量限(LOQ)总体上低于0.5。 ng / g,回收率在81-96%的范围内,相对标准偏差(RSD)低于20%。该方法还通过参加由FAPAS组织的国际可可脂能力测试(T0638)在2008年获得了优异的结果,从而进一步验证了该方法的真实性。所描述的方法获得的结果令人满意(z≤2)。该方法已用于测定实际食用油样品中的PAH。

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