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出 处:《铀矿冶》1992年第2期56-59,共4页Uranium Mining and Metallurgy
摘 要:试样预先经CL-TBP萃淋树脂分离大量的铀后,在三乙醇胺-氯化铵介质中,Ni(Ⅱ)和Co(Ⅱ)与了二酮肟形成络合物,分别于—1.05V和—1.30V(相对饱和甘汞电极)处产生灵敏的络合物吸附波。确定的最佳底液条件是0.2mol/L三乙醇胺-0.5mol/L氯化铵-0.02%丁二酮肟,pH为9.27,测定浓度范围Ni(Ⅱ)是0.002—0.1μS/ml,Co(Ⅱ)是0.003—0.1μS/ml。方法适用于八氧化三铀中微量Ni和Co的同时测定,精密度分别为±3.5%和±6.3%,加入回收分别为93%—105%和10%—96%。A simple and sensitive method has been proposed for the determination of Ni(Ⅱ) and Co(Ⅱ) in U3O8. As a result of the formation of electroactive complexes by the reaction of Ni(Ⅱ) and Co(Ⅱ) with diacetylaioxime in a suitable supporting electrolyte of 0. 2 mol/L triethanolamine,0. 5 mol/L ammonium muriate and 0. 02% diacetylaioxime,a sensitive adsorption wave appeared with peak patentials of Ni(Ⅱ) - 1. 05V and Co(Ⅱ) - 1. 30V (vs. S. C. E. ). The height of the adsorption wave was recti-linearly related to the concentration of Ni(Ⅱ) in the range 0. 002-0. 1 g/ml and Co(Ⅱ) in the range 0. 003 - 0. 1 g/ml. The separation of Ni(Ⅱ) and Co(Ⅱ) was carried out with CL-TBP extractant-containing resin. The precisions of the method for determination of Ni(Ⅱ) and Co(Ⅱ) were 3. 5% and 6. 3% respectively. The rates of recovery were 93-105% and 90 - 96% for Ni(Ⅱ) and Co (Ⅱ) respectively.
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