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硅胶预富集后用电感耦合等离子体质谱法测定海水中皮摩尔级铍含量

Determination of picomolar beryllium levels in seawater with inductively coupled plasma mass spectrometry following silica-gel preconcentration.

作者信息

Tazoe Hirofumi, Yamagata Takeyasu, Obata Hajime, Nagai Hisao

机构信息

Department of Radiation Chemistry, Institute of Radiation Emergency Mediation, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564, Japan; College of Humanities and Sciences, Nihon University, 3-25-40, Sakurajosui, Setagaya-ku, Tokyo 156-8550, Japan.

College of Humanities and Sciences, Nihon University, 3-25-40, Sakurajosui, Setagaya-ku, Tokyo 156-8550, Japan.

出版信息

Anal Chim Acta. 2014 Dec 10;852:74-81. doi: 10.1016/j.aca.2014.09.015. Epub 2014 Sep 16.

Abstract

A robust and rapid method for the determination of natural levels of beryllium (Be) in seawater was developed to facilitate mapping Be concentrations in the ocean. A solid-phase extraction method using a silica gel column was applied for preconcentration and purification of Be in seawater prior to determination of Be concentrations with inductively coupled plasma mass spectrometry (ICP-MS). Be was quantitatively adsorbed onto silica gel from solutions with pH values ranging from 6.3 to 9, including natural seawater. The chelating agent ethylenediamine tetraacetic acid was used to remove other ions in the seawater matrix (Na, Mg, and Ca) that interfere with the ICP-MS analysis. The reproducibility of the method was 3% based on triplicate analyses of natural seawater samples, and the detection limit was 0.4 pmol kg(-1) for 250 mL of seawater, which is sufficient for the analysis of seawater in the open ocean. The method was then used to determine the vertical profile of Be in the eastern North Pacific Ocean, which was found to be a recycled-type profile in which the Be concentration increased with depth from the surface (7.2 pmol kg(-1) at <200 m) to deep water (29.2 pmol kg(-1) from 3500 m to the bottom).

摘要

为便于绘制海洋中铍(Be)的浓度分布图,开发了一种稳健且快速的测定海水中天然铍含量的方法。在用电感耦合等离子体质谱法(ICP-MS)测定铍浓度之前,采用硅胶柱固相萃取法对海水中的铍进行预浓缩和净化。铍可从pH值范围为6.3至9的溶液(包括天然海水)中定量吸附到硅胶上。使用螯合剂乙二胺四乙酸去除海水中干扰ICP-MS分析的其他离子(Na、Mg和Ca)。基于对天然海水样品的三次重复分析,该方法的重现性为3%,对于250 mL海水,检测限为0.4 pmol kg(-1),这足以用于分析开阔海洋中的海水。然后使用该方法测定了北太平洋东部铍的垂直分布,发现其为一种循环型分布,即铍浓度从表层(<200 m处为7.2 pmol kg(-1))到深水(3500 m至海底为29.2 pmol kg(-1))随深度增加。

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