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首页> 外文期刊>Журнал аналитической химии >SPECTROPHOTOMETRY DETERMINATION OF MOLYBDENUM IN THE PRESENCE OF TUNGSTEN USING GALLEIN AND BENZYLDODECYLDIMETHYLAMMONIUM BROMIDE
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SPECTROPHOTOMETRY DETERMINATION OF MOLYBDENUM IN THE PRESENCE OF TUNGSTEN USING GALLEIN AND BENZYLDODECYLDIMETHYLAMMONIUM BROMIDE

机译:gallein和苄基十二烷基二甲基甲基铵分光光度法测定钨中的钼。

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The chemical similarity between molybdenum and tungsten makes the direct spectrophotometric determination of these metals impossible. Usually the determination is preceded by a separation step. In order to find out a selective and quantitative isolation method, coprecipitation with thioacetamide and Cu(II) as a carrier; Mn02; cupferron, tannin and crystal violet; quinolin-8-ol, tannin and thioacetamide, were examined. Mo-lybdenum(VI) could be determined in the presence of 100-fold mass excess of tungsten after precipitation with thioacetamide and Cu(II). The remaining methods could only be applied if mass excess of W is equal to or lower with respect to Mo. For the resolution of this problem, the derivative spectrophotometry was used. The studies ofdifferent order spectra of gallein complexes of molybdenum, tungsten and their mixtures have shown that the fifth-derivative spectra allows one to eliminate the interfering effects of Won the determination of Mo. At 650 nm the spectral features of tungsten is zeroing while the value of the fifth-derivative spectrum of mixture of Mo and W corresponds only to the concentration of molybdenum in the examined solution. Beer's law is obeyed in the range 0.32—0.80 ug/mL of Mo. The developed derivative spectrophotometric method and the most selective pre-separation method, based on the precipitation of molybdenum(VI) sulphide, were applied to the determination of Mo in Armco iron and steel. The accuracy of the elaborated methods was confirmed by comparison of the determined content of Mo with certified values as well as with the result obtained by the reference ICP-OES technique.
机译:钼和钨之间的化学相似性使得无法直接分光光度法测定这些金属。通常,在确定之前先进行分离步骤。为了找到一种选择性和定量的分离方法,以硫代乙酰胺和Cu(II)为载体共沉淀; MnO 2;铜铁,单宁和结晶紫;检查了喹啉-8-醇,单宁和硫代乙酰胺。用硫代乙酰胺和铜(II)沉淀后,钼(VI)的测定可以在钨过量100倍的条件下进行。仅当W的质量过量相对于Mo等于或小于Mo时,才可以使用其余方法。为解决此问题,使用了导数分光光度法。对钼,钨及其混合物的加仑复合物的不同阶光谱的研究表明,五阶导数光谱可以消除W对钼的测定的干扰作用。在650 nm处,钨的光谱特征为零,而Mo和W的混合物的五阶导数光谱的“平方”仅对应于所检查溶液中的钼浓度。在Mo的0.32-0.80 ug / mL范围内遵守比尔定律。将发达的分光光度法和基于硫化钼(VI)沉淀的最有选择性的预分离方法用于Armco中Mo的测定铁和钢。通过将测定的Mo含量与标准值以及通过参考ICP-OES技术获得的结果进行比较,可以确定详细方法的准确性。

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