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Determination of Ultratrace Impurities in High Purity Tantalum Materials by On-line Anion Exchange Matrix Separation and Inductively Coupled Plasma Mass Spectrometry

机译:在线阴离子交换基质分离-电感耦合等离子体质谱法测定高纯钽材料中的痕量杂质

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Ultratrace metal impurities (Be, Al, Ti, Cr, Ni, Nb, Mo, Sn, W, Th, and U) in high purity tantalum metal, tantalum(V) oxide, and tantalum pentaethoxide were determined by a combined system of flow injection with an anion exchange column and inductively coupled plasma mass spectrometry (ICP-MS). In the present combined system, the on-line matrix separation and multielement determination of impurity elements could be performed. When 2 M HCl/0.1 M HF mixed solution and 1 M HNO3/0.1 M HF mixed solution were used as the carrier solutions, Be, Al, and Ti for the former, and Cr, Ni, Nb, Mo, Sn, W, Th, and U for the latter were eluted from the column without any tantalum matrix. The detection limits (3σ) of analyte elements were in the range over 0.003 - 0.14 ng/ml as the sample solution basis. The present method was applied to the determination of metal impurities in high purity tantalum materials. The concentrations of Be, Ti, Mo, Sn, Th, and U were at the ng/g level, while those of other elements were in the range over the μg/g - ng/g level.
机译:高纯钽金属,氧化钽(V)和五氧化钽中的超痕量金属杂质(Be,Al,Ti,Cr,Ni,Nb,Mo,Sn,W,Th和U)是通过流动系统联合测定的阴离子交换柱和电感耦合等离子体质谱(ICP-MS)进样。在本组合系统中,可以进行在线矩阵分离和杂质元素的多元素确定。当使用2 M HCl / 0.1 M HF混合溶液和1 M HNO3 / 0.1 M HF混合溶液作为载体溶液时,前者为Be,Al和Ti,而Cr,Ni,Nb,Mo,Sn,W为后者的Th和U在没有任何钽基质的情况下从色谱柱中洗脱出来。以样品溶液为基准,分析物元素的检出限(3σ)在0.003-0.14 ng / ml范围内。本方法用于高纯钽材料中金属杂质的测定。 Be,Ti,Mo,Sn,Th和U的浓度为ng / g,而其他元素的浓度则在μg/ g-ng / g的范围内。

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