Ion pair-based dispersive liquid-liquid microextraction for gold determination at ppb level in solid samples after ultrasound-assisted extraction and in waters by electrothermal-atomic absorption spectrometry
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De la Calle, I.
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Pena-Pereira, F.
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Cabaleiro, N.
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Univ Vigo, Dept Quim Analit & Alimentaria, Area Quim Analit, Fac Quim, Vigo 36310, SpainUniv Vigo, Dept Quim Analit & Alimentaria, Area Quim Analit, Fac Quim, Vigo 36310, Spain
Cabaleiro, N.
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Lavilla, I.
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Bendicho, C.
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[1] Univ Vigo, Dept Quim Analit & Alimentaria, Area Quim Analit, Fac Quim, Vigo 36310, Spain
A new methodology was developed for the determination of ultratrace levels of gold in water samples, soils and river sediments. Dispersive liquid-liquid microextraction was used to preconcentrate the ion pair formed between AuCl4- and [CH3(CH2)(3)](4)N+ in a microliter-range volume of chlorobenzene using acetone as disperser solvent. When solid samples were analyzed, the method consisted of a combination of ultrasound-assisted extraction and dispersive liquid-liquid microextraction with final detection by electrothermal-atomic absorption spectrometry. Since an HCl medium was required for the formation of the AuCl4- complex, HCl together with HNO3 was used as extractants for ultrasound-assisted extraction. After optimization, the enrichment factor obtained was 220 for water samples. Moreover, the extraction efficiency was around 96%. The repeatability, expressed as relative standard deviation ranged from 3.6% to 9.7%. The instrumental detection limit was 8.4 ng L-1, whereas the procedural detection limits were 42 ng L-1 for water samples and 1.5 ng g(-1) for environmental solid samples. (C) 2010 Elsevier B.V. All rights reserved.