Yilmaz Vedat, Rose Lakeysha, Arslan Zikri, Little Maria D
Jackson State University, Department of Chemistry and Biochemistry, Jackson, MS 39217 USA. Tel: 01 (601)979-2072; ; Erciyes University, Faculty of Pharmacy, Department of Analytical of Chemistry, 38039 Kayseri, Turkey.
J Anal At Spectrom. 2012 Nov 1;27(11):1895-1902. doi: 10.1039/C2JA30195D.
A vapour generation (VG) procedure has been described for determination of Cd by ICP-MS. Volatile species of Cd were generated on-line by interacting acidic sample solution containing potassium hexacyanochromate(III), KCr(CN), with sodium borohydride (NaBH). The hexacyanochromate(III) complex was generated on-line by reacting 0.04 mol L chromium(III) nitrate and 0.16 mol L potassium cyanide (KCN) solutions in water. The resulting suspension of chromium(III) hydroxide, Cr(OH), was fed continuously to acidic stream of sample solution in the presence of excess KCN. The experimental conditions were optimized for effective generation of volatile species of Cd. Optimum signals were obtained from reaction of sample solutions in 4% v/v HCl with 2% m/v NaBH solution. Presence of KCr(CN) improved the efficiency of Cd vapour generation substantially affording 15-fold higher sensitivity. This phenomenon was thought to occur through formation of reactive intermediates evolved from interaction of [Cr(CN)] with NaBH that react with Cd(II) to increase the yield volatile Cd species. Under the optimum conditions, no significant interferences were observed from the transition metals, including Cu and Ni, up to 1.0 μg mL levels. Among the hydride forming elements, Bi, Pb, Sb and Sn depressed the signals above 0.1 μg mL. The detection limits (3s) were 6.2 and 5.2 ng L for Cd and Cd isotopes, respectively. The method was successfully applied to determination of Cd by ICP-MS in several certified reference materials, including Nearshore seawater (CASS-4), Bone ash (SRM 1400), Dogfish liver (DOLT-4) and Mussel tissue (SRM 2976).
已描述了一种用于通过电感耦合等离子体质谱法(ICP-MS)测定镉的蒸汽发生(VG)程序。通过使含有六氰合铬(III)酸钾(KCr(CN))的酸性样品溶液与硼氢化钠(NaBH)在线相互作用,生成镉的挥发性物种。六氰合铬(III)配合物通过在水中使0.04 mol/L硝酸铬(III)溶液和0.16 mol/L氰化钾(KCN)溶液反应在线生成。在过量KCN存在下,将所得氢氧化铬(III)(Cr(OH))悬浮液连续加入样品溶液的酸性流中。对实验条件进行了优化,以有效生成镉的挥发性物种。从4% v/v HCl中的样品溶液与2% m/v NaBH溶液的反应中获得了最佳信号。KCr(CN)的存在显著提高了镉蒸汽发生的效率,灵敏度提高了15倍。据认为,这种现象是通过[Cr(CN)]与NaBH相互作用产生的反应性中间体的形成而发生的,这些中间体与Cd(II)反应以提高挥发性镉物种的产率。在最佳条件下,对于高达1.0 μg/mL水平的包括铜和镍在内的过渡金属,未观察到明显干扰。在形成氢化物的元素中,铋、铅、锑和锡在高于0.1 μg/mL时会降低信号。镉和镉同位素的检测限(3s)分别为6.2和5.2 ng/L。该方法已成功应用于通过ICP-MS测定几种有证标准物质中的镉,包括近岸海水(CASS-4)、骨灰(SRM 1400)、角鲨肝(DOLT-4)和贻贝组织(SRM 2976)。