Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/6848
Title: Determination of lead in wine and rum samples by flow injection-hydride generation-atomic absorption spectrometry
Authors: Elçi, Latif
Arslan, Z.
Tyson, J.F.
Keywords: Flow injection
HG-AAS
Lead
Rum
Wine
Absorption
Absorption spectroscopy
Atomic absorption spectrometry
Atomic physics
Atomic spectroscopy
Catalyst activity
Hydrochloric acid
Oxide minerals
Potassium
Quartz
Sodium
Spectrometers
Spectrometry
Atomic absorption spectrometers
Atomic absorptions
Calibration curves
Detection limits
Direct determinations
Figures of merits
Flow injection hydrides
Hydride generations
Lead contents
Potassium ferricyanides
Red wines
Reductant
Regression coefficients
Relative errors
Relative standard deviations
Sample volumes
Sodium tetrahydroborate
hydrochloric acid
lead
potassium ferricyanide
sodium borohydride
atomic absorption spectroscopy
calibration
acidity
article
atomic absorption spectrometry
flow injection analysis
flow rate
mass spectrometry
red wine
rum
temperature
Alcoholic Beverages
Flow Injection Analysis
Sensitivity and Specificity
Spectrophotometry, Atomic
Abstract: A method for direct determination of lead in wine and rum samples was developed, using a flow injection hydride generation system coupled to an atomic absorption spectrometer with flame-quartz atomizer (FI-HG-AAS). Lead hyride (PbH4) was generated using potassium ferricyanide (K3Fe(CN)6), as oxidant and sodium tetrahydroborate (NaBH4) as reductant. Samples were acidified to 0.40% (v/v) HCl for wine and to 0.30% (v/v) HCl for rum, which were then mixed on-line with 3% (m/v) K3Fe(CN)6 solution in 0.03% (v/v) HCl prior to reaction with 0.2% (m/v) alkaline NaBH4 solution. Lead contents of a rum and two different red wine samples were determined by FI-HG-AAS agreed with those obtained by ICP-MS. The analytical figures of merit of method developed were determined. The calibration curve was linear up to 8.0 µg L-1 Pb with a regression coefficient of 0.998. The relative error was lower than 4.58%. The relative standard deviation (n = 7) was better than 12%. A detection limit of 0.16 µg L-1 was achieved for a sample volume of 170 µL. © 2008.
URI: https://hdl.handle.net/11499/6848
https://doi.org/10.1016/j.jhazmat.2008.05.113
ISSN: 0304-3894
Appears in Collections:Diğer Yayınlar Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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