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机构地区:[1]中国科学院长春应用化学研究所,长春市斯大林大街109号130022
出 处:《光谱实验室》1993年第4期30-32,共3页Chinese Journal of Spectroscopy Laboratory
摘 要:文章描述了荧光级氧化钇中痕量稀土铈的测定方法,在溴酸钾存在下,5摩尔/升HNO_3介质中,以P507萃取微量铈,然后有机相用硝酸、过氧化氢反萃取、再将水相浓缩定容,然后以电感耦合等离子体原子发射光谱法分析。同时用铈的离子选择电极以二次标准加入法作第二种手段分析。样品溶液以乙醇预去溶方式引入等离子体,测定下限为2微克/克,方法简单、快速、准确。离子选择电极法测定铈离子下限1×10~(-5)摩尔/升,回收率为94-101%,方法简单,结果满意、价格便宜。This paper describes determination method of trace rare earth cerium at fluorescence grade. Microcerium was extracted with P507 in potassium bromate and 5mol/L nitric acid. Organic phase was counterextracted with HNO_3 and H_2O_2. Water phase was concentrated and was quantitatived. This solu- tion was analyzed by inductively coupled plasma atomic emission spectro- metry. Cerium ion selective electrode double standard addition method was used as second analysis method. For inductively coupled plasma atomic emission spectrometry, the detection limit is 2 μg/g. This method is rapid and simple. The recovery is 94-101%. For the ion selective electrode method, the detection limits is 1×10_(-5)mol/L with satisfactory results.
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