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Development and initial evaluation of a combustion-based sample introduction system for direct isotopic analysis of mercury in solid samples via multi-collector ICP-mass spectrometry.
Bolea-Fernandez, Eduardo; Rua-Ibarz, Ana; Anjos, Jorge Alves; Vanhaecke, Frank.
Afiliação
  • Bolea-Fernandez E; Ghent University, Department of Chemistry, Atomic & Mass Spectrometry - A&MS Research Group, Campus Sterre, Krijgslaan 281-S12, 9000, Ghent, Belgium.
  • Rua-Ibarz A; Ghent University, Department of Chemistry, Atomic & Mass Spectrometry - A&MS Research Group, Campus Sterre, Krijgslaan 281-S12, 9000, Ghent, Belgium.
  • Anjos JA; Ghent University, Department of Chemistry, Atomic & Mass Spectrometry - A&MS Research Group, Campus Sterre, Krijgslaan 281-S12, 9000, Ghent, Belgium.
  • Vanhaecke F; Ghent University, Department of Chemistry, Atomic & Mass Spectrometry - A&MS Research Group, Campus Sterre, Krijgslaan 281-S12, 9000, Ghent, Belgium. Electronic address: frank.vanhaecke@ugent.be.
Talanta ; 276: 126210, 2024 Aug 15.
Article em En | MEDLINE | ID: mdl-38728804
ABSTRACT
High-precision isotopic analysis of mercury (Hg) using multi-collector ICP-mass spectrometry (MC-ICP-MS) is a powerful method for obtaining insight into the sources, pathways and sinks of this toxic metal. Modification of a commercially available mercury analyzer (Teledyne Leeman Labs, Hydra IIc - originally designed for quantification of Hg through sample combustion, collection of the Hg vapor on a gold amalgamator, subsequent controlled release of Hg and detection using cold vapor atomic absorption spectrometry CVAAS) enabled the system to be used for the direct high-precision Hg isotopic analysis of solid samples using MC-ICP-MS - i.e., without previous sample digestion and subsequent dilution. The changes made to the mercury analyzer did not compromise its (simultaneous) use for Hg quantification via CVAAS. The Hg vapor was mixed with a Tl-containing aerosol produced via pneumatic nebulization, creating wet plasma conditions, and enabling the use of Tl as an internal standard for correction of instrumental mass discrimination. Accurate and precise (0.10 ‰ 2SD, δ202Hg, n = 5) results were obtained for an in-house standard solution of Hg (20 ng Hg sample intake). Initial validation relied on the successful analysis of two solid certified reference materials of biological origin (BCR CRM 464 Tuna fish and NRC-CNRC TORT-3 Lobster hepatopancreas). It was shown that instrumental mass discrimination can be adequately corrected for by relying on the use of an aqueous Hg standard solution (NIST SRM 3133), without the need of matrix-matching. The novel setup developed thus allows for direct high-precision isotopic analysis of Hg in solid samples, thus enhancing the sample throughput. It is also suited for samples for which low amounts are available only and/or that are characterized by low Hg concentrations.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article