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首页> 外文期刊>Chemia Analityczna >Determination of total arsenic in traditional chinese medicines by flow injection hydride generation atomic fluorescence spectrometry
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Determination of total arsenic in traditional chinese medicines by flow injection hydride generation atomic fluorescence spectrometry

机译:流动注射氢化物发生原子荧光光谱法测定中药中总砷。

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The samples were digested with a mixture of nitric acid and perchloric acid. Suitable amount of thiourea was added to reduce As(V) to As(III), and to minimize the interference from transition metal ions. Total arsenic was determined after transformation to arseine by the reaction with KBH_4 solution. The interferences from Cu(II), Fe(III), Hg(II) and Se(IV) were studied and the mechanisms of interference were also discussed. In the flow injection mode the relative detection limit was 0.114 ng mL~(-1), which corresponds to an absolute detection limit of 0.034 ng. Quantification was investigated with both standard additions technique and a simple calibration curve method. The recoveries for the spiked 4 ng mL~(-1) As inthe studied medicines ranged from 95 to 105%. The precision for eleven replicate measurements was 0.68% (RSD) at the 5 ng mL~(-1) level. The developed method was successfully applied to the determination of total arsenic in a number of traditional Chinese medicines.
机译:样品用硝酸和高氯酸的混合物消化。加入适量的硫脲以将As(V)还原为As(III),并使过渡金属离子的干扰减至最小。通过与KBH_4溶液反应,将总砷确定为砷化氢。研究了Cu(II),Fe(III),Hg(II)和Se(IV)的干扰,并讨论了干扰机理。在流动注射模式下,相对检测限为0.114 ng mL〜(-1),对应于绝对检测限为0.034 ng。使用标准添加技术和简单的校准曲线方法对定量进行了研究。加标的4 ng mL〜(-1)As的回收率在95%至105%之间。在5 ng mL〜(-1)的水平下,十一次重复测量的精度为0.68%(RSD)。所开发的方法已成功地应用于多种中药中总砷的测定。

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