Evaluation of a microwave desolvation system in inductively coupled plasma mass spectrometry with low acid concentration solutions

Please use this identifier to cite or link to this item: http://hdl.handle.net/10045/13618
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Title: Evaluation of a microwave desolvation system in inductively coupled plasma mass spectrometry with low acid concentration solutions
Authors: Mora, Juan | Hernandis Martínez, Vicente | Veen, Eric H. van | Loos-Vollebregt, Margaretha T.C. de
Research Group/s: Espectrometría Atómica Analítica
Center, Department or Service: Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología | Delft University of Technology. Laboratory of Materials Science
Keywords: Microwave desolvation | Acid solution | Inductively coupled plasma mass spectrometry | Oxide level | Doubly-charged ion level | Polyatomic spectral interference
Knowledge Area: Química Analítica
Issue Date: Mar-1998
Publisher: Royal Society of Chemistry
Citation: MORA PASTOR, Juan, et al. “Evaluation of a microwave desolvation system in inductively coupled plasma mass spectrometry with low acid concentration solutions”. Journal of Analytical Atomic Spectrometry (JAAS). Vol. 13, Issue 3 (1998). ISSN 0267-9477, pp. 175-181
Abstract: The behaviour of a desolvation system based on microwave heating (termed a microwave desolvation system, MWDS) with low acid concentration solutions was evaluated in inductively coupled plasma mass spectrometry. Studies included water, sulfuric acid, perchloric acid, nitric acid and hydrochloric acid. The best performance of the MWDS was obtained at low liquid uptake rate and low acid concentrations. The analytical behaviour of the MWDS depends on the nature and composition of the solution used. In comparison with water, acid solutions provide up to four times higher ion intensities for the elements tested. In comparison with nitric and hydrochloric acid, sulfuric and perchloric acid provide higher ion intensities but also higher CeO+/Ce+ ratios whereas Ba2+/Ba+ ratios are lower. The limits of detection (LODs) are of the same order of magnitude for all acid solutions used, unless the specific isotope/solvent combinations suffer from spectral interference. In comparison with the conventional sample introduction (CS) without desolvation system the MWDS provides between 2 and 14 times higher ion intensities for the isotopes tested. For nitric and hydrochloric acid solutions the MWDS gives rise to lower CeO+/Ce+ratios and higher Ba2+/Ba+ ratios. For sulfuric and perchloric acid these tendencies are the opposite. For the isotopes that are not subject to interference, the LODs obtained with the MWDS are up to a factor of 10 lower than those obtained with CS.
Sponsor: DGICyT (Spain) (Project PB95–0693).
URI: http://hdl.handle.net/10045/13618
ISSN: 0267-9477 (Print) | 1364-5544 (Online)
DOI: 10.1039/a706833f
Language: eng
Type: info:eu-repo/semantics/article
Peer Review: si
Publisher version: http://dx.doi.org/10.1016/10.1039/a706833f
Appears in Collections:INV - GEAA - Artículos de Revistas

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