Determination of antimony by atomic absorption spectrometry with flow injection hydride generation by a tetrahydroborate-form anion-exchanger
Author(s) -
Yustina Rodriguez,
Julian F. Tyson
Publication year - 2006
Publication title -
journal of analytical atomic spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 113
eISSN - 1364-5544
pISSN - 0267-9477
DOI - 10.1039/b518042b
Subject(s) - chemistry , stibine , thiourea , antimony , amberlite , hydride , atomic absorption spectroscopy , detection limit , matrix (chemical analysis) , nuclear chemistry , inorganic chemistry , chromatography , adsorption , metal , catalysis , biochemistry , physics , organic chemistry , arsine , quantum mechanics , phosphine
A quartz tube atomic absorption spectrometric method for the determination of antimony by FI-HG was developed in which stibine (SbH3) was generated from the reaction between antimony in the injected solution and tetrahydroborate immobilized on a strong anion-exchange resin (Amberlite IRA-400). Several samples could be injected before the column was reloaded. The LOD (3s) in 4 mol l 1 HCl and 10% cysteine, and 4 mol l 1 HCl and 10% thiourea, were 0.55 and 0.54 m gl 1 , respectively. The precision, expressed as %RSD (n ¼ 5), was 5.9, 4.9, 3.8, 2.6 and 1.0 for 5.0, 10.0, 20.0, 40.0 and 60.0 m gl 1 , respectively, in 4 mol l 1 HCl and 10% (m/v) L-cysteine; and 8.1, 5.0, 1.5, 1.2 and 1.4 for the same concentrations in 4 mol l 1 HCl and 10% (m/v) thiourea. The throughput was 60 h 1 . Interferences from transition metals and hydride- forming elements, and signal suppression due to high ionic strength, were eliminated by the addition L-cysteine or thiourea to the samples, which also allowed the acid concentration to be decreased to 0.61 mol l 1 . The method was evaluated by the analysis of spiked sea and well waters, for which no matrix effects were observed: the recoveries for 3.0 and 5.0 m gl 1 were 102% and 110-114%, respectively.
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