Issue 8, 2009

High-precision cadmium stable isotope measurements by double spike thermal ionisation mass spectrometry

Abstract

Natural mass-dependent fractionation (MDF) of cadmium isotopes is a promising new tool for investigating Cd pathways and cycling in geological and biological materials. One interesting new application is as chemical tracer of deep water circulation and nutrient distribution in the oceans. But since natural isotope fractionation of Cd appears to be extremely limited and Cd abundances low, excellent external precision and sensitivity are needed to make full use of its potential. Here, we describe a newly-developed double spike (DS) method for determining the MDF of Cd isotopes. For inorganic matrices, samples are spiked with a mixed 106Cd-108Cd tracer prior to high-purity anion exchange-based separation of Cd. Isotope measurements are performed by TIMS using a silica gel activator. Overall, the DS-TIMS technique offers benefits in terms of superior precision and sensitivity compared to MC-ICPMS methods currently in use. External precisions on 100-ng-sized Cd standard loads, double spiked as unknowns, are ±14 ppm on the 112Cd/110Cd ratio (2SD), while ionization efficiencies (ions per atom loaded) are ∼0.3%. Using this technique, we calibrated the relative difference in MDF between several Cd standard materials used in various laboratories as “zero reference standards”. We also show that the 112Cd/110Cd ratio can be fractionated by as much as ∼0.2% by ion-exchange elution, which is potentially problematic for Cd isotope studies not using a double spike.

Graphical abstract: High-precision cadmium stable isotope measurements by double spike thermal ionisation mass spectrometry

Article information

Article type
Paper
Submitted
05 Dec 2008
Accepted
28 Apr 2009
First published
26 May 2009

J. Anal. At. Spectrom., 2009,24, 1079-1088

High-precision cadmium stable isotope measurements by double spike thermal ionisation mass spectrometry

A. Schmitt, S. J. G. Galer and W. Abouchami, J. Anal. At. Spectrom., 2009, 24, 1079 DOI: 10.1039/B821576F

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