An ICP-MS procedure to determine Cd, Co, Cu, Ni, Pb and Zn in oceanic waters using in-line flow-injection with solid-phase extraction for preconcentration

被引:61
作者
O'Sullivan, Jeanette E. [1 ,2 ,3 ]
Watson, Roslyn J. [1 ,2 ,3 ]
Butler, Edward C. V. [1 ,2 ,3 ,4 ,5 ]
机构
[1] CSIRO Wealth Oceans Natl Res Flagship, Hobart, Tas 7001, Australia
[2] Ctr Australian Weather & Climate Res, Hobart, Tas 7001, Australia
[3] CSIRO Marine & Atmospher Res, Hobart, Tas 7001, Australia
[4] Univ Tasmania, Antarctic Climate & Ecosyst CRC, Hobart, Tas 7001, Australia
[5] Australian Inst Marine Sci, Arafura Timor Res Facil, Casuarina, NT 0811, Australia
关键词
Automated; In-line; ICP-MS; Iminodiacetate; Trace elements; Seawater; PLASMA-MASS SPECTROMETRY; MARINE BIOGEOCHEMICAL CYCLES; TRACE-METALS; CHELATING RESIN; ONLINE PRECONCENTRATION; SEA-WATER; IMINODIACETATE RESIN; SOLVENT-EXTRACTION; HEAVY-METALS; SEAWATER;
D O I
10.1016/j.talanta.2013.06.054
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An automated procedure including both in-line preconcentration and multi-element determination by an inductively coupled plasma mass spectrometer (ICP-MS) has been developed for the determination of Cd, Co, Cu, Ni, Pb and Zn in open-ocean samples. The method relies on flow injection of the sample through a minicolumn of chelating (iminodiacetate) sorbent to preconcentrate the trace metals, while simultaneously eliminating the major cations and anions of seawater. The effectiveness of this step is tested and reliability in results are secured with a rigorous process of quality assurance comprising 36 calibration and reference samples in a run for analysis of 24 oceanic seawaters in a 6-h program. The in-line configuration and procedures presented minimise analyst operations and exposure to contamination. Seawater samples are used for calibration providing a true matrix match. The continuous automated pH measurement registers that chelation occurs within a selected narrow pH range and monitors the consistency of the entire analytical sequence. The eluent (0.8 M HNO3) is sufficiently strong to elute the six metals in 39 s at a flow rate of 2.0 mL/min, while being compatible for prolonged use with the mass spectrometer. Throughput is one sample of 7 mL every 6 min. Detection limits were Co 3.2 pM, Ni 23 pM, Cu 46 pM, Zn 71 pM, Cd 2.7 pM and Pb 1.5 pM with coefficients of variation ranging from 3.4% to 8.6% (n=14) and linearity of calibration established beyond the observed concentration range of each trace metal in ocean waters. Recoveries were Co 96.7%, Ni 102%, Cu 102%, Zn 98.1%, Cd 92.2% and Pb 97.6%. The method has been used to analyse similar to 800 samples from three voyages in the Southern Ocean and Tasman Sea. It has the potential to be extended to other trace elements in ocean waters. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:999 / 1010
页数:12
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