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First order speciation of vanadium and chromium in water samples by on-line continuous membrane separation hyphenated to inductively coupled plasma mass spectrometry

机译:通过在线连续膜分离联用电感耦合等离子体质谱法对水样中的钒和铬进行一阶形态分析

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An on-line anion-exchange membrane separation system has been coupled to inductively coupled plasma mass spectrometry (ICP-MS) for the total vanadium(V) and chromium (Cr) determination and V(IV) and Cr(III) species determination simultaneously. The positive charged V(IV) and Cr(III) species have been efficiently separated from V(V) and Cr(VI), and selectively determined by the on-line electrodialyzer-ICP-MS. To determine the total concentrations of V and Cr in water samples, H2SO4 and Na2S2O3 were added to convert all vanadium and chromium species into their positive species, thus, V(V) and Cr(VI) in the samples were quantified by subtraction. The cool plasma and reaction gas can also be avoided as the severe interference from chloride, carbon and nitrogen-based molecular ion has been substantially suppressed by the anion-exchange membrane. The detection limits of the analytes were 0.02 μg L~(-1) for V(IV) and 0.06 μg L~(-1) for Cr(III) with this on-line system, respectively, and the relative standard deviation (n = 10) of 10 μg L~(-1) V(IV) and Cr(III) were 3.7% and 2.1%, respectively. The developed method has been applied for the speciation of V and Cr in three water samples, with V(V) and Cr(III) found as the main species in these samples. The accuracy and feasibility of this method have also been verified by spike tests and a certified reference material (CRM) of environmental water (GSBZ 50029-94) and a CRM of riverine water (GBW 08608), good recoveries have been obtained and the analytical results are also in good agreement with the certified values.
机译:在线阴离子交换膜分离系统已与电感耦合等离子体质谱(ICP-MS)结合使用,可同时测定总钒(V)和铬(Cr)以及同时测定V(IV)和Cr(III)种类。带正电的V(IV)和Cr(III)种类已从V(V)和Cr(VI)中有效分离出来,并通过在线电渗析仪ICP-MS进行选择性测定。为了确定水中样品中V和Cr的总浓度,添加了H2SO4和Na2S2O3将所有钒和铬物种转化为它们的阳性物种,因此,通过减法对样品中的V(V)和Cr(VI)进行了定量。由于阴离子交换膜已基本上抑制了氯,碳和氮基分子离子的严重干扰,因此还可避免冷等离子体和反应气体。该在线系统对V(IV)的分析物的检出限分别为0.02μgL〜(-1)和Cr(III)的0.06μgL〜(-1),相对标准偏差(n 10μgL〜(-1)中的V(IV)和Cr(III)= 10)分别为3.7%和2.1%。所开发的方法已用于三个水样品中V和Cr的形态分析,其中V(V)和Cr(III)是这些样品中的主要物种。该方法的准确性和可行性还通过加标测试,环境水的认证参考材料(CRM)(GSBZ 50029-94)和河水的CRM(GBW 08608)进行了验证,已获得了良好的回收率并进行了分析。结果也与认证值高度吻合。

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