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 |
Show full item record
CORE Recommender
SCOPUSTM
Citations
43
checked on Oct 13, 2024
WEB OF SCIENCETM
Citations
37
checked on Nov 22, 2024
Page view(s)
62
checked on Aug 24, 2024
Google ScholarTM
Check
Altmetric
Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.