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在线阴离子交换/共沉淀分离基体后,用电感耦合等离子体质谱法测定高纯钽材料中的痕量磷。

Determination of trace phosphorus in high purity tantalum materials by inductively coupled plasma mass spectrometry subsequent to matrix separation with on-line anion exchange/coprecipitation.

作者信息

Kozono Shuji, Takahashi Shigeto, Haraguchi Hiroki

机构信息

Analysis and Physical Properties Center, Showa Denko K.K., Chiba, Japan.

出版信息

Anal Bioanal Chem. 2002 Feb;372(4):542-8. doi: 10.1007/s00216-001-1145-2. Epub 2001 Dec 21.

DOI:10.1007/s00216-001-1145-2
PMID:11939629
Abstract

An on-line matrix separation/inductively coupled plasma mass spectrometry (ICP-MS) method is proposed for the determination of trace amounts of phosphorus in high purity tantalum metal, tantalum (V) oxide, and tantalum pentaethoxide. In the present method, the matrix tantalum in the sample solution was adsorbed on the anion exchange resin, and phosphorus (phosphate ion) was eluted with the carrier solution of HF and HNO3 mixture. Then, the effluent solution was subsequently mixed with bismuth solution and aqueous ammonia solution to coprecipitate phosphate together with bismuth hydroxide. The precipitate formed was collected on the in-line membrane filter to wash out nitric acid with pure water, and then dissolved with hydrochloric acid. The obtained phosphorus sample solution was introduced directly into the nebulizer of ICP-MS for the determination of phosphorus. Phosphorus was determined at the molecular ion signal of 31P16O+ (m/z 47). The detection limit (3sigma) of phosphorus in the present method was 1.3 ng mL(-1) as the sample solution basis, and the relative standard deviation for 30 ng mL(-1) of phosphorus in the standard solution was 4.3% in the replicate measurements (n=11). The present method was applied to the analysis of high purity tantalum materials. The concentrations of phosphorus in tantalum samples were in fairly good agreement with those obtained by glow discharge mass spectrometry (GDMS).

摘要

提出了一种在线基质分离/电感耦合等离子体质谱法(ICP-MS),用于测定高纯钽金属、五氧化二钽和五乙氧基钽中的痕量磷。在本方法中,样品溶液中的基质钽吸附在阴离子交换树脂上,磷(磷酸根离子)用HF和HNO3混合载液洗脱。然后,流出液随后与铋溶液和氨水溶液混合,使磷酸盐与氢氧化铋共沉淀。形成的沉淀收集在在线膜过滤器上,用纯水冲洗掉硝酸,然后用盐酸溶解。将得到的磷样品溶液直接引入ICP-MS的雾化器中进行磷的测定。磷在31P16O+(m/z 47)的分子离子信号处测定。本方法中磷的检测限(3σ)以样品溶液为基础为1.3 ng mL(-1),标准溶液中30 ng mL(-1)磷的重复测量(n=11)的相对标准偏差为4.3%。本方法应用于高纯钽材料的分析。钽样品中磷的浓度与辉光放电质谱法(GDMS)得到的结果相当吻合。

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