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Sensitive differential pulse polarographic determination of molybdenum using the new catalytic system Mo(VI)-phenantroline-chlorate

机译:新的催化体系Mo(VI)-菲咯啉-氯酸盐灵敏微分脉冲极谱法测定钼

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摘要

It was found that in acidic chloride media the complex of Mo(VI) with 1,10-phenantroline induces catalytic reduction of KClO3. This catalytic effect can be utilized for sensitive differential pulse polarographic determination of Mo(VI) with a low detection limit of 2.9 x 10(-11) M (2.8 ng/L). The optimal Mo(Vl) response was obtained at pH 2.8, in the presence of (6-12) X 10(-5) M 1,10-phenantroline and 2 x 10(-2) M KClO3. ne sensitivity was 1.73 nAM and the catalytic response was linear up to 7.5 x 10(-7) M Mo (VI). The interferences from inorganic ions and surface-active substances were investigated. The results of the determination of Mo(Vl) in CRM water sample showed good reproducibility (R.S.D. for standard solution is below 1.2% and for water samples is 8.9%) and accuracy of the elaborated catalytic polarographic method.
机译:发现在酸性氯化物介质中,Mo(VI)与1,10-菲咯啉的络合物可诱导KClO3催化还原。这种催化作用可用于检测限为2.9 x 10(-11)M(2.8 ng / L)的Mo(VI)的灵敏差分脉冲极谱法测定。在(6-12)X 10(-5)M 1,10-菲咯啉和2 x 10(-2)M KClO3存在下,在pH 2.8时获得了最佳的Mo(VI)反应。 ne灵敏度为1.73 nA / nM,催化反应在7.5 x 10(-7)M Mo(VI)下呈线性关系。研究了无机离子和表面活性物质的干扰。 CRM水样品中Mo(VI)的测定结果显示出良好的重现性(标准溶液的R.S.D.低于1.2%,水样品的R.S.D.)和精密催化极谱法的准确性。

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