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利用顺序注射分析的自动在线固相萃取-电热原子吸收光谱法测定人尿样中的痕量钒、镉和铅

Automatic On-line Solid-phase Extraction-Electrothermal Atomic Absorption Spectrometry Exploiting Sequential Injection Analysis for Trace Vanadium, Cadmium and Lead Determination in Human Urine Samples.

作者信息

Giakisikli Georgia, Ayala Quezada Alejandro, Tanaka Junpei, Anthemidis Aristidis N, Murakami Hiroya, Teshima Norio, Sakai Tadao

出版信息

Anal Sci. 2015;31(5):383-9. doi: 10.2116/analsci.31.383.

Abstract

A fully automated sequential injection column preconcentration method for the on-line determination of trace vanadium, cadmium and lead in urine samples was successfully developed, utilizing electrothermal atomic absorption spectrometry (ETAAS). Polyamino-polycarboxylic acid chelating resin (Nobias chelate PA-1) packed into a handmade minicolumn was used as a sorbent material. Effective on-line retention of chelate complexes of analytes was achieved at pH 6.0, while the highest elution effectiveness was observed with 1.0 mol L(-1) HNO3 in the reverse phase. Several analytical parameters, like the sample acidity, concentration and volume of the eluent as well as the loading/elution flow rates, have been studied, regarding the efficiency of the method, providing appropriate conditions for the analysis of real samples. For a 4.5 mL sample volume, the sampling frequency was 27 h(-1). The detection limits were found to be 3.0, 0.06 and 2.0 ng L(-1) for V(V), Cd(II) and Pb(II), respectively, with the relative standard deviations ranging between 1.9 - 3.7%. The accuracy of the proposed method was evaluated by analyzing a certified reference material (Seronorm(TM) trace elements urine) and spiked urine samples.

摘要

利用电热原子吸收光谱法(ETAAS)成功开发了一种全自动顺序注射柱预富集方法,用于在线测定尿液样本中的痕量钒、镉和铅。将填充到自制微型柱中的聚氨基多羧酸螯合树脂(Nobias螯合PA-1)用作吸附材料。在pH 6.0时实现了分析物螯合物的有效在线保留,而在反相中用1.0 mol L(-1) HNO3观察到最高的洗脱效率。关于该方法的效率,研究了几个分析参数,如样品酸度、洗脱液浓度和体积以及进样/洗脱流速,为实际样品分析提供了合适的条件。对于4.5 mL的样品体积,进样频率为27 h(-1)。发现V(V)、Cd(II)和Pb(II)的检测限分别为3.0 ng L(-1)、0.06 ng L(-1)和2.0 ng L(-1),相对标准偏差在1.9% - 3.7%之间。通过分析有证标准物质(Seronorm(TM)微量元素尿液)和加标尿液样本评估了该方法的准确性。

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