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首页> 外文期刊>ChemPlusChem >Quantification of 3-Monochloropropane-1,2-diol Esters in Edible Oils by Large-Volume Injection Coupled to Comprehensive Gas Chromatography-Time-of-Flight Mass Spectrometry
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Quantification of 3-Monochloropropane-1,2-diol Esters in Edible Oils by Large-Volume Injection Coupled to Comprehensive Gas Chromatography-Time-of-Flight Mass Spectrometry

机译:通过大容量注射液相传到食用油中3-二氯丙烷-1,2-二醇酯的量化与综合气相色谱 - 飞行时间的质谱法

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摘要

3-Monochloropropane-1,2-diol (3-MCPD) esters are a group of process contaminants formed during the refining of edible oils and fats. A method for the determination of 3-MCPD esters in such oils and fats based on large-volume injection-comprehensive gas chromatography-time-of-flight mass spectrometry (LVI-GC x GC-ToF MS) is presented. The simplified method for sample preparation consists of alkaline hydrolysis followed by extraction of 3-MCPD from the lipid matrix and derivatization using phenylboronic acid. The limit of detection was 0.8 mu g kg(-1), reported as free 3-MCPD. The repeatability was better than 2.7% relative standard deviation for levels around 0.5 mu g g(-1) 3-MCPD. The GC x GC-ToF MS system was shown to be stable over 100 analyses.
机译:3-二氯丙烷-1,2-二醇(3-MCPD)酯是在精炼食用油和脂肪中形成的一组工艺污染物。 提出了一种基于大容量注射综合气相色谱 - 飞行时间质谱(LVI-GC X GC-TOF MS)在这种油和脂肪中测定3-MCPD酯的方法。 样品制备的简化方法由碱性水解组成,然后用苯硼酸从脂质基质中提取3-MCPD,并使用苯硼酸衍生化。 检测限为0.8μgkg(-1),报告为自由3-mcpd。 可重复性优于2.7%的相对标准偏差,水平约为0.5μg(-1)3-MCPD。 GC X GC-TOF MS系统显示在100个分析上稳定。

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