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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Rapid screening of edible oils for phthalates using phase-transfer catalyst-assisted hydrolysis and liquid phase microextraction coupled to high performance liquid chromatography-tandem mass spectrometry
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Rapid screening of edible oils for phthalates using phase-transfer catalyst-assisted hydrolysis and liquid phase microextraction coupled to high performance liquid chromatography-tandem mass spectrometry

机译:使用相转移催化剂辅助水解和液相微萃取与高效液相色谱-串联质谱联用快速筛选邻苯二甲酸盐的食用油

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摘要

Edible oil is easily contaminated with phthalic acid esters (PAEs). Conventional procedures to analyze individual PAEs require very rigorous experimental conditions that are extremely labor-intensive due to significant procedural contaminations generated by the ubiquitous presence of PAEs in the laboratory environment. In this study, a rapid screening method for PAEs in edible oil was successfully developed. Using a phase-transfer catalyst (terabutylammonium bromide) during oil/water biphasic base hydrolysis of PAEs, the hydrolysis time was decreased from a previously reported time of 20h to 10 min (80 degrees C). The resulting phthalic acid in the acidified hydrolysate was extracted with 600 mu L of tributyl phosphate and then analyzed by high performance liquid chromatography-tandem mass spectrometry in 6 min. Parameters affecting the hydrolysis of PAEs and the extraction of phthalic acid were optimized, and the analytical method was validated. No obvious matrix effect existed in the edible oils whether an external or internal standard method was used. The detection limit was 1.0 mu mol kg(-1), and the quantification limit was 1.3 mu mol kg(-1). The recovery rates varied from 86 to 107% with relative standard deviations equal to or lower than 9.9% in all of the tested conditions. Twenty-six samples were analyzed, and the background corrected total PAE content was found to be in the range of
机译:食用油容易被邻苯二甲酸酯(PAE)污染。用于分析单个PAE的常规程序需要非常严格的实验条件,由于实验室环境中普遍存在的PAE会产生严重的程序污染,因此这是非常劳动密集型的。在这项研究中,成功​​开发了一种快速筛选食用油中PAE的方法。在PAE的油/水双相碱水解过程中使用相转移催化剂(溴化叔丁基铵),水解时间从先前报道的20小时减少至10分钟(80摄氏度)。用600μL磷酸三丁酯萃取酸化水解产物中的邻苯二甲酸,然后在6分钟内通过高效液相色谱-串联质谱分析。优化了影响PAEs水解和邻苯二甲酸萃取的参数,并验证了分析方法。无论采用外标法还是内标法,食用油中均不存在明显的基质效应。检出限为1.0μmol kg(-1),定量限为1.3μmol kg(-1)。在所有测试条件下,回收率在86%至107%之间变化,相对标准偏差等于或小于9.9%。分析了26个样品,发现经背景校正的总PAE含量在

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