Tyszczuk Katarzyna, Korolczuk Mieczyslaw
Faculty of Chemistry, Maria Curie-Sklodowska University, Maria Curie-Sklodowska Sq. 3, 20-031 Lublin, Poland.
Anal Chim Acta. 2008 Aug 29;624(2):232-7. doi: 10.1016/j.aca.2008.06.044. Epub 2008 Jul 4.
An in situ plated lead film electrode has been applied for adsorptive stripping voltammetric determination of trace concentrations of molybdenum in the presence of Alizarin S. The procedure is based on the preconcentration of the molybdenum-Alizarin S complex at an in situ plated lead film electrode held at -0.6 V (versus Ag/AgCl), followed by a negatively sweeping square wave voltammetric scan. The peak current is proportional to the concentration of molybdenum over the range 2x10(-9) to 5x10(-8) mol L(-1), with a 3sigma detection limit of 9x10(-10) mol L(-1) with an accumulation time of 60 s. The measurements were carried out from underaerated solutions. The proposed procedure was validated in the course of Mo(VI) determination in water certified reference materials.
一种原位镀铅膜电极已被用于在茜素S存在下吸附溶出伏安法测定痕量钼。该方法基于在-0.6 V(相对于Ag/AgCl)的原位镀铅膜电极上预富集钼-茜素S络合物,随后进行负向扫描的方波伏安扫描。在2×10⁻⁹至5×10⁻⁸ mol L⁻¹范围内,峰电流与钼浓度成正比,在60 s的积累时间下,3σ检测限为9×10⁻¹⁰ mol L⁻¹。测量是在欠曝气溶液中进行的。该方法在水标准参考物质中钼(VI)的测定过程中得到了验证。