This work explores the multi-element capabilities of inductively coupled plasma-mass spectrometry with collision/reaction cell technology (CCT-ICP-MS) for the simultaneous determination of both spectrally interfered and non-interfered nuclides in wine samples using a single set of experimental conditions. The influence of the cell gas type (i.e. He, He+H-2 and He+NH3), cell gas flow rate and sample pre-treatment (i.e. water dilution or acid digestion) on the background-equivalent concentration (BEC) of several nuclides covering the mass range from 7 to 238 u has been studied. Results obtained in this work show that, operating the collision/reaction cell with a compromise cell gas flow rate (i.e. 4 mL min(-1)) improves BEC values for interfered nuclides without a significant effect on the BECs for non-interfered nuclides, with the exception of the light elements Li and Be. Among the different cell gas mixtures tested, the use of He or He+H-2 is preferred over He+NH3 because NH3 generates new spectral interferences. No significant influence of the sample pre-treatment methodology (i.e. dilution or digestion) on the multi-element capabilities of CCT-ICP-MS in the context of simultaneous analysis of interfered and non-interfered nuclides was observed. Nonetheless, sample dilution should be kept at minimum to ensure that light nuclides could be quantified in wine. Finally, a direct 5-fold aqueous dilution is recommended for the simultaneous trace and ultra-trace determination of spectrally interfered and non-interfered elements in wine by means of CCT-ICP-MS. The use of the CCT is mandatory for interference-free ultra-trace determination of Ti and Cr. Only Be could not be determined when using the CCT due to a deteriorated limit of detection when compared to conventional ICP-MS. (C) 2014 Elsevier B.V. All rights reserved.
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Univ Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
Univ Mississippi, Natl Ctr Nat Prod Res, Oxford, MS 38677 USAUniv Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
Duzgoren-Aydin, Nurdan S.
Avula, Bharathi
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Univ Mississippi, Natl Ctr Nat Prod Res, Oxford, MS 38677 USAUniv Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
Avula, Bharathi
Willett, Kristine L.
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Univ Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
Univ Mississippi, Natl Ctr Nat Prod Res, Oxford, MS 38677 USA
Univ Mississippi, Dept Pharmacol, Oxford, MS 38677 USAUniv Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
Willett, Kristine L.
Khan, Ikhlas A.
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Univ Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
Univ Mississippi, Natl Ctr Nat Prod Res, Oxford, MS 38677 USA
Univ Mississippi, Sch Pharm, Dept Pharmacognosy, Oxford, MS 38677 USAUniv Mississippi, Environm Toxicol Res Program, Oxford, MS 38677 USA
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Univ Utah, Dept Pathol, Hlth Sci Ctr, Salt Lake City, UT 84108 USA
ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USAUniv Utah, Dept Pathol, Hlth Sci Ctr, Salt Lake City, UT 84108 USA
Johnson-Davis, Kamisha L.
Farnsworth, Candice
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ARUP Labs, 500 Chipeta Way,MS-115, Salt Lake City, UT 84108 USAUniv Utah, Dept Pathol, Hlth Sci Ctr, Salt Lake City, UT 84108 USA
Farnsworth, Candice
Law, Christian
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ARUP Labs, 500 Chipeta Way,MS-115, Salt Lake City, UT 84108 USAUniv Utah, Dept Pathol, Hlth Sci Ctr, Salt Lake City, UT 84108 USA
Law, Christian
Parker, Rebecca
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ARUP Labs, 500 Chipeta Way,MS-115, Salt Lake City, UT 84108 USAUniv Utah, Dept Pathol, Hlth Sci Ctr, Salt Lake City, UT 84108 USA