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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1039/c5ja00157a</dc:identifier><dc:language>eng</dc:language><dc:creator>Bolea-Fernandez, E.</dc:creator><dc:creator>Balcaen, L.</dc:creator><dc:creator>Resano, M.</dc:creator><dc:creator>Vanhaecke, F.</dc:creator><dc:title>Tandem ICP-mass spectrometry for Sr isotopic analysis without prior Rb/Sr separation</dc:title><dc:identifier>ART-2016-93139</dc:identifier><dc:description>The use of a mixture of 10% of CH3F and 90% of He as a reaction gas in tandem ICP-mass spectrometry (ICP-MS/MS) enables the accurate determination of the 87Sr/86Sr isotope ratio in geological materials, provided that mass discrimination is corrected for by using a combination of internal (Russell law, assuming a constant 88Sr/86Sr isotope ratio) and external correction (using the isotopic reference material NIST SRM 987 SrCO3) in a sample-standard bracketing approach. No prior Rb/Sr separation is required as the isobaric overlap at a mass-to-charge ratio of 87 is avoided by monitoring SrF+ reaction product ions instead of Sr+ ions. Rb shows no reactivity towards CH3F. The double mass selection (MS/MS mode) prevents both spectral overlap from atomic ions at the mass-to-charge ratios of SrF+ reaction product ions and a measurable effect from the matrix on the 87Sr/86Sr result. This aspect is critical, as it enables accurate results to be obtained without the need for using a matrix-matched standard to correct for mass discrimination, in contrast to previous work with a quadrupole ICP-MS instrument with a CH3F/Ne-pressurized cell, in which the use of a matrix-matched standard was compulsory. The precision attainable-0.05% RSD external precision-suffices for making the newly developed method useful in a variety of applications.</dc:description><dc:date>2016</dc:date><dc:source>http://zaguan.unizar.es/record/131508</dc:source><dc:doi>10.1039/c5ja00157a</dc:doi><dc:identifier>http://zaguan.unizar.es/record/131508</dc:identifier><dc:identifier>oai:zaguan.unizar.es:131508</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2012-33494</dc:relation><dc:identifier.citation>Journal of Analytical Atomic Spectrometry 31, 1 (2016), 303-310</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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