Determination of Cu, Mn, Ni and Sn in gasoline by electrothermal vaporization inductively coupled plasma mass spectrometry, and emulsion sample introduction
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作者:
Saint'Pierre, TD
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机构:Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
Saint'Pierre, TD
Dias, LF
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机构:Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
Dias, LF
Pozebon, D
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机构:Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
Pozebon, D
Aucélio, RQ
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机构:Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
Aucélio, RQ
Curtius, AJ
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Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, BrazilUniv Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
Curtius, AJ
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Welz, B
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机构:Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
Welz, B
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[1] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
[2] UFRGS, Inst Quim, BR-91500915 Porto Alegre, RS, Brazil
[3] Pontificia Univ Catolica Rio de Janeiro, Dept Quim, BR-22453900 Rio De Janeiro, Brazil
Trace metals in fuels, except in the case of additives, are usually undesirable and normally they occur in very low concentrations in gasoline, requiring sensitive techniques for their determination. Coupling of electrothermal vaporization with inductively coupled plasma mass spectrometry minimizes the problems related to the introduction of organic solvents into the plasma. Furthermore, sample preparation as oil-in-water emulsions reduces problems related to gasoline analysis. In this work, a method for determination of Cu, Mn, Ni and Sn in gasoline is proposed. Samples were prepared by forming a 10-fold diluted emulsion with a surfactant (Triton X-100), after treatment with concentrated HNO3. The sample emulsion was pre-concentrated in the graphite tube by repeated pipetting and drying. External calibration was used with aqueous standards in a purified gasoline emulsion. Six samples from different gas stations were analyzed, and the analyte concentrations were found to be in the mug l(-1) range or below. The limits of detection were 0.22, 0.02, 0.38 and 0.03 mug l(-1) for Cu, Mn, Ni and Sn, respectively. The accuracy of the method was estimated using a recovery test. (C) 2002 Elsevier Science B.V. All rights reserved.
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Natl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, CanadaNatl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, Canada
Sturgeon, RE
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Lam, JW
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Natl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, CanadaNatl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, Canada
机构:
Natl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, CanadaNatl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, Canada
Sturgeon, RE
;
Lam, JW
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Natl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, CanadaNatl Res Council Canada, Inst Natl Measurement Stand, Ottawa, ON K1A 0R9, Canada