Determination of antimony in plant and peat samples by hydride generation-atomic fluorescence spectrometry (HG-AFS)

被引:39
作者
Chen, B [1 ]
Krachler, M [1 ]
Shotyk, W [1 ]
机构
[1] Univ Heidelberg, Inst Environm Geochem, D-69120 Heidelberg, Germany
关键词
D O I
10.1039/b306597a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A robust and sensitive analytical procedure for the determination of Sb in plant and peat samples using hydride generation-atomic fluorescence spectrometry (HG-AFS) has been developed. The hydride generation of Sb was carried out by using 1% (m/v) of NaBH4 and 4 mol l(-1) HCl. The analytical procedure was critically evaluated by analysing five certified plant reference materials (BCR CRM 281 Rye Grass, CTA-VTL-2 Virginia Tobacco Leaves, GBW 07602 Bush Branches and Leaves, SRM 1547 Peach Leaves and SRM 1515 Apple Leaves) and two in-house peat reference materials. The accuracy and precision ( <3%) of the developed procedure was evaluated by the determination of Sb in certified reference materials, two in-house reference materials, and showed good agreement with the reference and information values. Prior to HG-AFS, 200 mg aliquots of dried samples were digested with 3 ml nitric acid, 0.5 ml hydrogen peroxide and 0.1 ml tetrafluoroboric acid (HBF4) using closed-pressurized digestion in a microwave oven. The efficiency of applying HBF4 for destroying silicates in the samples was also investigated. The digests of the samples were first diluted to 10 ml using high purity water, subsequently mixed with 1 ml of 50 g l(-1) L-cysteine for the pre-reduction of Sb(v) in the digests, and finally diluted to 50 ml using 4 mol l(-1) hydrochloric acid for measurement. A solution detection limit of 8 ng l(-1) was obtained using the optimised experimental conditions which corresponds to a method detection limit of 2 ng g(-1) in solid peat: this detection limit is far lower than those previously reported for this element using the identical HG-AFS instrument. The newly developed analytical procedure has been applied to the determination of Sb in ancient peat samples collected from remote Scottish peat bogs. The high sea salt content of these peat samples caused no matrix interferences. Comparison of the results obtained using HG-AFS with instrumental neutron activation analysis (INAA) data obtained previously shows that the lower limits of detection of INAA are unsuitable for measuring Sb in pre-anthropogenic samples.
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页码:1256 / 1262
页数:7
相关论文
共 22 条
[1]   THE GEOCHEMISTRY OF ANTIMONY AND ITS USE AS AN INDICATOR ELEMENT IN GEOCHEMICAL PROSPECTING [J].
BOYLE, RW ;
JONASSON, IR .
JOURNAL OF GEOCHEMICAL EXPLORATION, 1984, 20 (03) :223-302
[2]   DETERMINATION OF ANTIMONY(III,V) IN NATURAL-WATERS BY SEPARATION AND PRECONCENTRATION ON A THIONALIDE LOADED RESIN FOLLOWED BY NEUTRON-ACTIVATION ANALYSIS [J].
CHWASTOWSKA, J ;
ZMIJEWSKA, W ;
STERLINSKA, E .
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-ARTICLES, 1995, 196 (01) :3-9
[3]   Improving the analytical performance of hydride generation non-dispersive atomic fluorescence spectrometry. Combined effect of additives and optical filters [J].
D'Ulivo, A ;
Bramanti, E ;
Lampugnani, L ;
Zamboni, R .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2001, 56 (10) :1893-1907
[4]   Determination of antimony in soils and vegetables by hydride generation atomic fluorescence spectrometry and electrothermal atomic absorption spectrometry. Optimization and comparison of both analytical techniques [J].
De Gregori, I ;
Pinochet, H ;
Fuentes, E ;
Potin-Gautier, M .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (02) :172-178
[5]   Antimony speciation at ultra trace levels using hydride generation atomic fluorescence spectrometry and 8-hydroxyquinoline as an efficient masking agent [J].
Deng, TL ;
Chen, YW ;
Belzile, N .
ANALYTICA CHIMICA ACTA, 2001, 432 (02) :293-302
[6]  
Emsley J., 2001, NATURE BUILDING BLOC
[7]   DIRECT-DETECTION OF ANTIMONY IN ENVIRONMENTAL AND BIOLOGICAL SAMPLES AT TRACE CONCENTRATIONS BY LASER-INDUCED FLUORESCENCE IN GRAPHITE-FURNACE WITH AN INTENSIFIED CHARGE-COUPLED-DEVICE [J].
ENGER, J ;
MARUNKOV, A ;
CHEKALIN, N ;
AXNER, O .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1995, 10 (08) :539-549
[8]   Antimony in the environment: a review focused on natural waters I. Occurrence [J].
Filella, M ;
Belzile, N ;
Chen, YW .
EARTH-SCIENCE REVIEWS, 2002, 57 (1-2) :125-176
[9]   Determination of total antimony and antimony(V) by inductively coupled plasma mass spectrometry after selective separation of antimony(III) by solvent extraction with N-benzoyl-N-phenylhydroxylamine [J].
Garbos, S ;
Bulska, E ;
Hulanicki, A ;
Fijalek, Z ;
Soltyk, K .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2000, 55 (07) :795-802
[10]   Optimized procedure for the determination of antimony in lipid-rich environmental matrices by flow injection hydride generation atomic absorption spectrometry [J].
Krachler, M ;
Burow, M ;
Emons, H .
ANALYST, 1999, 124 (06) :923-926