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

被引:44
作者
De la Calle, I. [1 ]
Pena-Pereira, F. [1 ]
Cabaleiro, N. [1 ]
Lavilla, I. [1 ]
Bendicho, C. [1 ]
机构
[1] Univ Vigo, Dept Quim Analit & Alimentaria, Area Quim Analit, Fac Quim, Vigo 36310, Spain
关键词
Ultrasound-assisted extraction; Dispersive liquid-liquid microextraction; Gold; ng g(-1) levels; Environmental samples; CLOUD POINT EXTRACTION; PHASE MICROEXTRACTION; TRACE AMOUNTS; ENVIRONMENTAL-SAMPLES; PRECIOUS METALS; PALLADIUM; CHEMISTRY; SOLVENT;
D O I
10.1016/j.talanta.2010.12.031
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
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.
引用
收藏
页码:109 / 115
页数:7
相关论文
共 35 条
[1]
Utility of solid phase extraction for spectrophotometric determination of gold in water, jewel and ore samples [J].
Amin, Alaa S. .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2010, 77 (05) :1054-1058
[2]
Development of a sequential injection dispersive liquid-liquid microextraction system for electrothermal atomic absorption spectrometry by using a hydrophobic sorbent material: Determination of lead and cadmium in natural waters [J].
Anthemidis, Aristidis N. ;
Ioannou, Kallirroy-Ioanna G. .
ANALYTICA CHIMICA ACTA, 2010, 668 (01) :35-40
[3]
On-line sequential injection dispersive liquid-liquid microextraction system for flame atomic absorption spectrometric determination of copper and lead in water samples [J].
Anthemidis, Aristidis N. ;
Ioannou, Kallirroy-Ioanna G. .
TALANTA, 2009, 79 (01) :86-91
[4]
Green Analytical Chemistry [J].
Armenta, S. ;
Garrigues, S. ;
de la Guardia, M. .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2008, 27 (06) :497-511
[6]
Determination of the precious metals in geological materials by inductively coupled plasma mass spectrometry [J].
Barefoot, RR .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1998, 13 (10) :1077-1084
[7]
BRAVO O, 1967, ANAL CHIM ACTA, V47, P209
[8]
A low-cost flame atomic absorption spectrometry method for determination of trace metals in aqueous samples [J].
Carasek, E .
TALANTA, 2000, 51 (01) :173-178
[9]
Recent development in liquid phase microextraction for determination of trace level concentration of metals-A review [J].
Dadfarnia, Shayessteh ;
Shabani, Ali Mohammad Haji .
ANALYTICA CHIMICA ACTA, 2010, 658 (02) :107-119
[10]
SOLVENT-EXTRACTION OF GOLD [J].
DAS, NR ;
BHATTACHARYYA, SN .
TALANTA, 1976, 23 (07) :535-540