Issue 7, 2011

MC-ICPMS isotope ratio measurements using an ultra-low flow sample introduction system

Abstract

This study characterises for the first time isotope ratio measurements by multi-collector ICPMS when performed at liquid flow rates as low as 10–15 µL min−1. An evolution of the torch integrated sample introduction system (TISIS) was employed, which combined an OpalMist nebulizer and a heated single pass spray chamber, allowing the transport of almost 100% of the solvent. The different factors potentially influencing the isotope ratio measured values and the associated sources of uncertainty (sensitivity and interferences, mass discrimination effects, repeatability of isotope ratio measurement, and rinsing time and memory effects) were investigated systematically under varying experimental conditions. Results showed that the liquid flow rate has a large impact on mass discrimination effects, making the control of this variable critical. From 5 to 30 µL min−1, when using the exponential model, the mass discrimination per mass unit changed from −1.6 to −2.1 and from −1.1 to −1.9, for 88Sr+/86Sr+ and 208Pb+/206Pb+ ratios respectively. Moreover, extrapolations from these results lead to the conclusion that a syringe pump may be required instead of a free aspiration regime to control the liquid flow rate and eliminate the possibility of undesired variations of isotope ratio results (typically, 0.05‰ error for 1–2% fluctuations at 10 µL min−1). The validity of the exponential model also depends on the experimental conditions selected. When working at 15 µL min−1 and heating the chamber walls at 60–80 °C, the performance was as good as it could be with a MicroMist/water cooled cinnabar combination operated at 200 µL min−1 (thus, the efficiency was 12 times better for the TISIS). Both systems were compared for the measurement of the Sr isotopic signature in honey samples. Since the TISIS allowed for a preconcentration of samples by a factor 5, the combined uncertainty on results could be improved by 1.6 to 4.4. The main drawback was, however, the longer rinsing time required to reach a stable background signal (10–12 minutes rather than 4).

Graphical abstract: MC-ICPMS isotope ratio measurements using an ultra-low flow sample introduction system

Article information

Article type
Paper
Submitted
15 Dec 2010
Accepted
18 Feb 2011
First published
14 Mar 2011

J. Anal. At. Spectrom., 2011,26, 1372-1379

MC-ICPMS isotope ratio measurements using an ultra-low flow sample introduction system

E. Paredes, D. G. Asfaha, E. Ponzevera, C. Brach-Papa, M. Van Bocxstaele, J. L. Todolí and C. R. Quétel, J. Anal. At. Spectrom., 2011, 26, 1372 DOI: 10.1039/C0JA00254B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements