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Determination of arsenic and mercury in Chinese medicinal herbs by atomic fluorescence spectrometry with closed-vessel microwave digestion

机译:封闭容器微波消解-原子荧光光谱法测定中草药中的砷和汞

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摘要

A simple method was developed for the determination of trace arsenic and mercury in Chinese medicinal herbs. The samples were digested in closed-Teflon vessels in a microwave oven, and followed with hydride generation atomic fluorescence spectrometric measurements. The experimental conditions for the digestion were carefully optimized using an orthogonal design. The accuracy of the method was validated by recovery experiments, and the analytical results for arsenic in seven medicinal herbs (Codonopsis pilosula, Radix angelicae sinensis, Aconitum carmichaeli debx, crude aconite root, giant typhonium rhizome, Rhizoma typhonii, and Radix aconiti lateralis preparata) were found to agree well with those by inductively coupled plasma atomic emission spectrometry (ICP-AES). The linear dynamic range of the calibration curve was in the range of 0.1-400 ng/mL for arsenic, and the correlation coefficient was better than 0.999. The limit of detection was 0.1 ng/mL for arsenic. For mercury, the determination was accomplished through mercury cold vapor generation in the same instrumental system. The linear dynamic range was 0.03-250 ng/mL, with a limit of detection of 0.03 ng/mL for mercury. This was a rapid, convenient, precise, and cost-effective method.
机译:建立了一种测定中草药中痕量砷和汞的简单方法。样品在微波炉的密闭特氟隆容器中消化,然后进行氢化物发生原子荧光光谱测量。使用正交设计仔细地优化了消化的实验条件。通过回收率实验验证了该方法的准确性,并分析了七种药材(党参,当归,乌头乌头,粗附子,巨型typ根,鼠伤根和附子)中砷的分析结果。通过电感耦合等离子体原子发射光谱法(ICP-AES),发现它们与这些化合物非常吻合。砷的校准曲线的线性动态范围在0.1-400 ng / mL范围内,相关系数优于0.999。砷的检出限为0.1 ng / mL。对于汞,测定是通过在同一仪器系统中产生汞冷蒸气来完成的。线性动态范围为0.03-250 ng / mL,汞的检出限为0.03 ng / mL。这是一种快速,方便,精确且具有成本效益的方法。

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