Issue 8, 2005

Determination of U, Th and Pu in natural waters, biological materials and clinical samples by ETV-ICP-MS

Abstract

A method for the determination of U, Th and Pu in natural water, biological materials and urine samples by electrothermal vaporization inductively coupled plasma mass spectrometry (ETV-ICP-MS) is described. Carbide formation was minimized using sample vaporization from a tantalum surface for U and additional use of tetrafluoromethane (Freon-23) as a gaseous modifier for Th and Pu. A prior Ca3(PO4)2 co-precipitation provided an enrichment factor of 50, yielding procedural detection limits (LOD) of 0.013, 0.029 and 0.017 pg g−1 for Th, U and Pu, respectively and corresponding absolute LODs of 0.13, 0.29 and 0.17 fg. Recovery of spikes from urine was typically 80%, whereas those from seawater, river water and biological materials averaged 99%. The accuracy of the method was validated by determination of U and Th in NIST SRM 1566b Oyster Tissue and U in a series of NRC natural water CRMs SLRS-4, CASS-4, NASS-5 and SLEW-3. Precision of determination was better than 10% at concentrations of 0.1 ng mL−1.

Graphical abstract: Determination of U, Th and Pu in natural waters, biological materials and clinical samples by ETV-ICP-MS

Article information

Article type
Paper
Submitted
21 Feb 2005
Accepted
26 May 2005
First published
20 Jun 2005

J. Anal. At. Spectrom., 2005,20, 717-723

Determination of U, Th and Pu in natural waters, biological materials and clinical samples by ETV-ICP-MS

P. Grinberg, S. Willie and R. E. Sturgeon, J. Anal. At. Spectrom., 2005, 20, 717 DOI: 10.1039/B502550H

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