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采用氨诱导氢氧化镁共沉淀反应池电感耦合等离子体质谱法测定海水中溶解态金属的痕量水平。

Determination of ultratrace levels of dissolved metals in seawater by reaction cell inductively coupled plasma mass spectrometry after ammonia induced magnesium hydroxide coprecipitation.

机构信息

Department of Chemistry and Industrial Chemistry, University of Genoa, Genoa, Italy.

出版信息

Anal Chim Acta. 2011 Nov 7;706(1):84-8. doi: 10.1016/j.aca.2011.07.046. Epub 2011 Aug 9.

Abstract

A method for the determination of ultratrace amounts of Cr, Fe, Mn, Pb and Zn in seawater has been developed. It combined the low-blank magnesium hydroxide coprecipitation procedure with quadrupole inductively coupled plasma mass spectrometry and used the dynamic reaction cell technique to resolve the polyatomic interferences arising from the residual matrix, the solvent and plasma gases. Detection limits (3σ(B), n=10) for Cr, Fe, Mn, Pb and Zn were 0.02, 0.10, 0.01, 0.002 and 0.19 nM, respectively, using 50 mL of seawater sample. The accuracy of the analytical procedure was verified by the analysis of the seawater reference materials CASS-4, NASS-5, SAFe D2 and SAFe S. The analytical precision ranged from 3% to 16% (n=6), with a sample throughput of about 6 samples h(-1).

摘要

已经开发出一种用于测定海水中痕量 Cr、Fe、Mn、Pb 和 Zn 的方法。该方法将低空白氢氧化镁共沉淀程序与四极电感耦合等离子体质谱法相结合,并使用动态反应池技术来解决由残留基质、溶剂和等离子体气体引起的多原子干扰。使用 50 毫升海水样品,Cr、Fe、Mn、Pb 和 Zn 的检测限(3σ(B),n=10)分别为 0.02、0.10、0.01、0.002 和 0.19 nM。通过对海水参考物质 CASS-4、NASS-5、SAFe D2 和 SAFe S 的分析,验证了分析程序的准确性。分析精度范围为 3%至 16%(n=6),样品通量约为 6 个样品 h(-1)。

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