首页> 外文期刊>Bulletin of the Korean Chemical Society >Determination of Methylmercury in Biological Samples Using Dithizone Extraction Method Followed by Purge & Trap GC-MS
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Determination of Methylmercury in Biological Samples Using Dithizone Extraction Method Followed by Purge & Trap GC-MS

机译:双硫zone萃取法-吹扫捕集-GC-MS法测定生物样品中的甲基汞

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摘要

In this study,a dithizone extraction technique involving purge & trap GC-MS was developed for the determination of methylmercury in biological samples,especially blood and fish.After alkaline digestion,methylmercury in biological samples was extracted into dithizone and back-extracted into aqueous sulfide solution.The extracted methylmercury was converted to the volatile ethyl derivative,purged and trapped onto a solid-phase collection medium,and then introduced into the GC-MS system.The determined MDLs of the established method were 0.9 ng·g~(-1) for biological samples and its accuracy and precision were found to be 93% and 3.8%,respectively.The method was validated by analysis of CRMs such as SRM 966,BCR 463 and IAEA 407 and all analytical results were within certified ranges with average RSDs of less than 6%.The analytical results of field-sampled fish also showed that the method can be successfully used as an alternative for commonly used distillation method followed by GC-CVAFS detection.
机译:本研究开发了一种吹扫捕集GC-MS的双硫zone萃取技术,用于测定生物样品(尤其是血液和鱼类)中的甲基汞。碱性消​​化后,将生物样品中的甲基汞萃取到双硫th中并反萃取到硫化氢水溶液中萃取出的甲基汞被转化为挥发性乙基衍生物,吹扫并截留在固相收集介质中,然后引入GC-MS系统。所建立方法的MDLs为0.9 ng·g〜(-1) )的生物样品,其准确度和精密度分别为93%和3.8%。该方法通过对CRM(例如SRM 966,BCR 463和IAEA 407)的分析进行了验证,所有分析结果均在标准RSD的认证范围内不到6%。现场采样鱼的分析结果还表明,该方法可以成功替代常用的蒸馏方法,然后再进行GC-CVAFS de检测。

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