Issue 21, 2025

Iodine determination by ICP-MS following platinum-assisted photochemical vapor generation: a strategy to overcome condensed-phase interferences

Abstract

Data on the use of Pt2+ in the ion-assisted photochemical vapor generation of iodine with detection using inductively coupled plasma mass spectrometry (ICP-MS) are presented. Certified reference materials (antarctic krill, milk powder and oyster tissue) were acid-digested using a mixture of HNO3 and H2O2 and subsequently spiked with 0.5 mg L−1 Pt2+. The digested samples were then diluted to contain 10% (v/v) CH3COOH and irradiated using a Hg lamp with the main emission line at 253.7 nm in a quartz photoreactor. The nitric acid interference on the photochemical generation of volatile iodine species was evaluated in the range 0–5% (v/v). Signal suppression, likely due to NO3 and/or the formation of NO2, was overcome for solutions containing between 0.3 and 0.7 mol L−1 HNO3 upon adding Pt2+ to the solution. The presence of Pt2+ has also provided a ca. 85% signal enhancement for iodine in comparison with solutions without Pt2+. The samples were analyzed following calibration against aqueous standards, which is a definite advantage over many PVG methods reported in the literature and further evidence of Pt2+ efficiency in suppressing condensed phase interferences under the adopted conditions. The determined analyte concentrations in the CRM were all in good statistical agreement with the certified values, demonstrating the good accuracy of the method.

Graphical abstract: Iodine determination by ICP-MS following platinum-assisted photochemical vapor generation: a strategy to overcome condensed-phase interferences

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Article information

Article type
Paper
Submitted
25 Feb 2025
Accepted
25 Apr 2025
First published
06 May 2025

Anal. Methods, 2025,17, 4443-4450

Iodine determination by ICP-MS following platinum-assisted photochemical vapor generation: a strategy to overcome condensed-phase interferences

R. M. de Oliveira, B. S. Soares and D. L. G. Borges, Anal. Methods, 2025, 17, 4443 DOI: 10.1039/D5AY00318K

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