Jackson State University, Department of Chemistry and Biochemistry, Jackson, MS 39217, USA.
Anal Chim Acta. 2013 Jan 25;761:18-26. doi: 10.1016/j.aca.2012.11.039. Epub 2012 Nov 29.
A hydride generation (HG) procedure has been described for determination of Pb by ICP-MS using potassium hexacyanomanganate(III), K(3)Mn(CN)(6), as an additive to facilitate the generation of plumbane (PbH(4)). Potassium hexacyanomanganate(III) was prepared in acidic medium as it was unstable in water. The stability of hexacyanomanganate(III) was examined in dilute solutions of HCl, HNO(3) and H(2)SO(4). The solutions prepared in 1% v/v H(2)SO(4) were found to be stable for over a period of 24h. The least suitable medium was 1% v/v HNO(3). For generation of plumbane, acidic hexacyanomanganate(III) and sample solutions were mixed on-line along a 5-cm long tygon tubing (1.14 mm i.d.) and then reacted with 2% m/v sodium borohydride (NaBH(4)). A concentration of 0.5% m/v K(3)Mn(CN)(6) facilitated the generation of PbH(4) remarkably. In comparison to H(2)SO(4), HCl provided broader working range for which optimum concentration was 1% v/v. No significant interferences were noted from transition metals and hydride forming elements, up to 0.5 μg mL(-1) levels, except Cu which depressed the signals severely. The depressive effects in the presence of 0.1 μg mL(-1) Cu were alleviated by increasing the concentration of K(3)Mn(CN)(6) to 2% m/v. Under these conditions, the sensitivity was enhanced by a factor of at least 42 to 48. The detection limit (3s) was 0.008 μg L(-1) for (208)Pb isotope. Average signal-to-noise ratio (S/N) ranged between 18 and 20 for 1.0 μg mL(-1) Pb solution. The accuracy of the method was verified by analysis of several certified reference materials, including Nearshore seawater (CASS-4), Bone ash (SRM 1400), and Mussel tissue (SRM 2976). The procedure was also successfully applied to the determination of Pb in coastal seawater samples by ICP-MS.
一种氢化物发生(HG)程序已被描述为使用六氰合锰酸钾(III),K(3)Mn(CN)(6),通过 ICP-MS 测定 Pb,以促进生成(PbH(4))。在酸性介质中制备六氰合锰酸钾(III),因为它在水中不稳定。在稀盐酸,HNO(3)和 H(2)SO(4)溶液中检查了六氰合锰酸钾(III)的稳定性。发现用 1%v/v H(2)SO(4)制备的溶液在超过 24 小时的时间内稳定。最不合适的介质是 1%v/v HNO(3)。为了生成(PbH(4)),在线将酸性六氰合锰酸钾(III)和样品溶液混合在 5 厘米长的 tygon 管(1.14mm i.d.)中,然后与 2%m/v 硼氢化钠(NaBH(4))反应。浓度为 0.5%m/v K(3)Mn(CN)(6)可显著促进 PbH(4)的生成。与 H(2)SO(4)相比,HCl 提供了更宽的工作范围,最佳浓度为 1%v/v。直到 0.5μgmL(-1)水平,除了严重抑制信号的 Cu 之外,过渡金属和形成氢化物的元素没有观察到明显的干扰。存在 0.1μgmL(-1)Cu 时的抑制作用通过将 K(3)Mn(CN)(6)的浓度增加到 2%m/v 而得到缓解。在这些条件下,灵敏度提高了至少 42 到 48 倍。对于(208)Pb 同位素,检测限(3s)为 0.008μg L(-1)。对于 1.0μgmL(-1)Pb 溶液,平均信号与噪声比(S/N)在 18 到 20 之间。通过分析几种认证的参考物质,包括近岸海水(CASS-4),骨灰(SRM 1400)和贻贝组织(SRM 2976),验证了该方法的准确性。该程序还成功地应用于通过 ICP-MS 测定沿海海水中的 Pb。