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使用填充有改性碳纳米纤维的微柱与电感耦合等离子体质谱联用,用于生物样品中痕量稀土元素的同时在线预富集和测定。

Use of a microcolumn packed with modified carbon nanofibers coupled with inductively coupled plasma mass spectrometry for simultaneous on-line preconcentration and determination of trace rare earth elements in biological samples.

作者信息

Chen Shizhong, Xiao Mingfa, Lu Dengbo, Zhan Xilin

机构信息

Key Laboratory, Wuhan Polytechnic University, Wuhan 430023, China.

出版信息

Rapid Commun Mass Spectrom. 2007;21(15):2524-8. doi: 10.1002/rcm.3123.

DOI:10.1002/rcm.3123
PMID:17610216
Abstract

In this work, a new method was developed for the determination of trace rare earth elements (REEs) in biological samples by inductively coupled plasma mass spectrometry (ICP-MS) after preconcentration on a microcolumn packed with modified carbon nanofibers (CNFs). CNFs oxidized with nitric acid have been proved to possess an exceptional adsorption capability for REEs due to their surface functionalization. The effects of the experimental parameters, including pH, sample flow rate and volume, elution solution and interfering ions, on the recoveries of the analytes have been investigated systematically. A 100-fold enrichment factor was obtained. The adsorption capacity of CNFs was found to be 18.1, 19.3, 23.6, 17.6, 22.3 and 19.5 mg/g for La, Ce, Sm, Eu, Dy and Y, respectively. Under the optimum conditions, the detection limits of this method ranged from 0.2 pg/mL (Dy) to 1.2 pg/mL (Ce) with an enrichment factor of 15-fold, and the relative standard deviations (RSDs) for the determination of REEs at the 1.0 ng/mL level were less than 4% (n = 9). This method was applied to the analysis of trace REEs in a real sample of human hair with recoveries of 95-115%. In order to validate the proposed method, a certified reference material of human hair (GBW 07601) was analyzed with satisfactory results.

摘要

在本工作中,开发了一种新方法,用于在填充有改性碳纳米纤维(CNF)的微柱上预富集后,通过电感耦合等离子体质谱法(ICP-MS)测定生物样品中的痕量稀土元素(REE)。已证明用硝酸氧化的CNF由于其表面功能化而对REE具有出色的吸附能力。系统研究了实验参数,包括pH值、样品流速和体积、洗脱溶液和干扰离子,对分析物回收率的影响。获得了100倍的富集因子。发现CNF对La、Ce、Sm、Eu、Dy和Y的吸附容量分别为18.1、19.3、23.6、17.6、22.3和19.5 mg/g。在最佳条件下,该方法的检测限为0.2 pg/mL(Dy)至1.2 pg/mL(Ce),富集因子为15倍,在1.0 ng/mL水平下测定REE的相对标准偏差(RSD)小于4%(n = 9)。该方法应用于实际人发样品中痕量REE的分析,回收率为95-115%。为了验证所提出的方法,对人发标准参考物质(GBW 07601)进行了分析,结果令人满意。

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