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Determination of Trace Cobalt in Water by Microwave Digestion-Catalytic fading Spectrophotometry

机译:微波消化催化褪色分光光度法测定水中痕量钴

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A simple and sensitive catalytic fading spectrophometry was developted for determination the trace cobalt in water treated by microwave digestion. The method is based on catalysis of cobalt on the oxidation of acid chrome blue K by potassium periodate with polyethylene glycol-200 as an activator in boric acid-sodium borate buffer solution. Major factors such as microwave digestion conditions, kinds and dosages of media, reagents and activators, the reaction temperature, the reaction time and coexisting irons were investigated and the optimal experimental conditions are determination wavelength 525 nm, at 80°C reacton for 12 min. The linear range and the detection limit of the method are determinated. The maximum relative standard deviation is 5.68%, and the recoveries are 96.4% to 105.9%. The maximum relative error compared with GB (national standard of china 3838-2002) is below 5.52%.
机译:利用简单敏感的催化褪色分光谱法测定微波消解处理的水中痕量钴。 该方法基于聚乙二醇-200用聚乙二醇-20作为硼酸钠硼酸钠缓冲溶液中的活化剂的酸铬蓝钾催化剂的催化物分析。 研究了诸如微波消化条件,种类和剂量的主要因素,试剂和活化剂,反应温度,反应时间和共存铁杆,并且最佳实验条件是测定波长525nm,在80℃反应器中进行12分钟。 确定方法的线性范围和检测限。 最大相对标准偏差为5.68%,回收率为96.4%至105.9%。 与GB相比的最大相对误差(中国国家标准3838-2002)低于5.52%。

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