首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >The spectrophotometric determination of trace molybdenum (VI) after collection and elution as molybdate ion on protonated chitin.
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The spectrophotometric determination of trace molybdenum (VI) after collection and elution as molybdate ion on protonated chitin.

机译:分光光度法测定质子化甲壳质上的钼离子在收集和洗脱后的痕量钼(VI)。

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摘要

Collection and elution method for inorganic anion on protonated chitin has been applied to the spectrophotometric determination of molybdenum (VI). The Mo (VI) is collected as molybdate ion on a column of chitin in weak acidic medium which is easilyeluted with a small volume of 0.1 M ammonia buffer solution (pH 10). The Mo (VI) in the eluent is determined by bromopyrogallol red-Zephiramine method spectrophotometrically. Beer's law is obeyed over the concentration range Mo (VI) 0.1-0.8μg/ml eluentat 634 nm. The apparent molar absorptivity is 6 X 104 dm3 mol-1 cm-1. The tolerance limits for WO2-4, VO3-, CrO2-4 and Fe (III) is low, that is, 1-100 times that of Mo (VI), but some metal ions and common inorganic anions do not interfere in concentration range of 1000-5000 times that of Mo (VI). The present method can be applied to the determination of Mo (VI) in natural water samples.
机译:质子化几丁质上无机阴离子的收集和洗脱方法已用于分光光度法测定钼(VI)。 Mo(VI)以钼酸根离子的形式收集在弱酸性介质中的几丁质柱上,该溶液很容易用少量的0.1 M氨水缓冲溶液(pH 10)洗脱。洗脱液中的Mo(VI)通过溴邻苯三酚红-Zephiramine方法分光光度法测定。在634 nm处洗脱液Mo(VI)0.1-0.8μg/ ml的浓度范围内遵守比尔定律。表观摩尔吸收率为6 X 104 dm3 mol-1 cm-1。 WO2-4,VO3-,CrO2-4和Fe(III)的容许限很低,即Mo(VI)的容许限的1-100倍,但某些金属离子和常见的无机阴离子不会干扰浓度范围是Mo(VI)的1000-5000倍本方法可用于测定天然水样中的Mo(VI)。

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