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Mercury(II) and methylmercury determination in water by liquid chromatography hyphenated to cold vapour atomic fluorescence spectrometry after online short-column preconcentration

机译:在线短柱预富集-冷蒸气原子荧光光谱法联用液相色谱法测定水中的汞(II)和甲基汞

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This paper reports a method developed for the simultaneous determination of methylmercury (MeHg+) and mercury(II) (Hg2+) species in water by liquid chromatography coupled to online UV irradiation and cold vapour atomic fluorescence spectrometry (LC-UV-CV-AFS) after online short-column preconcentration. This work focused on systematic studies of several variables to establish the maximum species recoveries, preconcentration factors and good reproducibility. The optimum results obtained were the following: 0.07 mmol L-1 2-mercaptoethanol as a complexing agent, precolumn conditioning with the mobile phase: a mixture of 80% of methanol (MeOH) and 20% of the following buffer: 0.0015 mol L-1 ammonium pyrrolidine dithiocarbamate (APDC) and 0.01 mol L-1 ammonium acetate (NH4CH3COO) at pH 5.5, 2 cm precolumn length and 2 mL min(-1) sample flow. This method was applied to three water samples with different mineralisation contents. Various tests, based on spikes, were performed on each sample. A breakthrough volume of 4 mL was found. The recovery values of 72 +/- 3% and 81 +/- 5% for MeHg+ and Hg2+, respectively, were obtained regardless of the matrix composition, and the PF values were 30 and 32 for MeHg+ and Hg2+, respectively. The accuracy of the preconcentration method was verified by analysing a certified reference material. The detection limits (LDs) obtained were 15 ng L-1 for MeHg+ and 2 ng L-1 for Hg2+. The quantification limits (LQs) were 50 ng L-1 for both species. The established analytical online preconcentration method is suitable for the quantification of mercury species in a wide range of environmental waters.
机译:本文报道了一种通过液相色谱-在线紫外辐射和冷蒸气原子荧光光谱法(LC-UV-CV-AFS)联用同时测定水中甲基汞(MeHg +)和汞(II)(Hg2 +)种类的方法在线短柱预浓缩。这项工作集中于对几个变量的系统研究,以建立最大的物种回收率,预浓缩因子和良好的再现性。获得的最佳结果如下:0.07 mmol L-1 2-巯基乙醇作为络合剂,用流动相进行预柱预处理:80%的甲醇(MeOH)和20%的以下缓冲液的混合物:0.0015 mol L- 1吡咯烷二硫代氨基甲酸铵(APDC)和0.01 mol L-1乙酸铵(NH4CH3COO)在pH 5.5,柱前2 cm长和2 mL min(-1)样品流下。该方法适用于三个矿化含量不同的水样。对每个样品进行基于加标的各种测试。发现突破体积为4 mL。无论基质组成如何,MeHg +和Hg2 +的回收率分别为72 +/- 3%和81 +/- 5%,MeHg +和Hg2 +的PF值分别为30和32。通过分析认证的参考物质,验证了预浓缩方法的准确性。获得的检测限(LDs)对于MeHg +为15 ng L-1,对于Hg2 +为2 ng L-1。两种物种的定量限(LQ)为50 ng L-1。建立的在线分析富集方法适用于定量各种环境水中的汞种类。

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