Determination of platinum and rhodium in environmental matrixes by solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry

被引:41
作者
Vanhaecke, F [1 ]
Resano, M [1 ]
Pruneda-Lopez, M [1 ]
Moens, L [1 ]
机构
[1] State Univ Ghent, Analyt Chem Lab, Inst Nucl Sci, B-9000 Ghent, Belgium
关键词
D O I
10.1021/ac020378a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrothermal vaporization from a graphite furnace was used in combination with inductively coupled plasma mass spectrometry (ICPMS) for the determination of Pt and Rh in environmental matrixes. Solid samples of tunnel dust, grass, and atmospheric aerosol collected on a cellulose filter could be analyzed directly, such that sample dissolution-which is not self-evident for the determination of platinum group metals-could be avoided. By heating the graphite furnace according to a multistep temperature program, spectral interferences were avoided, since a "dry" plasma was obtained, while "parent" ions such as Cu, Zn, and Pb, giving origin to interfering molecular ions, were vaporized during the thermal pretreatment step. For tunnel dust, the most demanding sample matrix, a mixture of HCl and HF was used as a modifier to stimulate the vaporization of matrix components during the thermal pretreatment step and, hence, to alleviate matrix-induced. analyte signal suppression during the actual vaporization step. Calibration was accomplished by means of single standard addition with an aqueous standard solution. The results obtained agreed within the experimental uncertainty with the corresponding reference values (certified values or results obtained using pneumatic nebulization ICPMS), while relative standard deviations of less than or equal to 15% were typical for both Pt and Rh. In all samples, a Pt/Rh ratio of approximately 6-8 was established. For a typical sample mass of 2 mg, limits of detection were 0.35 ng/gfor Pt and 0.05 ng/g for Rh.
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页码:6040 / 6048
页数:9
相关论文
共 54 条
[1]   PLATINUM TRACES IN AIRBORNE PARTICULATE MATTER - DETERMINATION OF WHOLE CONTENT, PARTICLE-SIZE DISTRIBUTION AND SOLUBLE PLATINUM [J].
ALT, F ;
BAMBAUER, A ;
HOPPSTOCK, K ;
MERGLER, B ;
TOLG, G .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1993, 346 (6-9) :693-696
[2]   Determination of platinum at trace levels in environmental and biological materials [J].
Barefoot, RR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (02) :309-314
[3]  
BEAUCHEMIN D, 2000, DISCRETE SAMPLE INTR, pCH3
[4]   Determination of physiological platinum levels in human urine using magnetic sector field inductively coupled plasma mass spectrometry in combination with ultraviolet photolysis [J].
Begerow, J ;
Turfeld, M ;
Dunemann, L .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1996, 11 (10) :913-916
[5]   Theoretical evaluation of solid sampling electrothermal atomic absorption spectrometry for screening purposes [J].
Belarra, MA ;
Resano, M ;
Castillo, JR .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1999, 14 (04) :547-552
[6]   EVALUATION OF A MOLECULAR RECOGNITION LIGAND FOR PERFORMING THE EXTRACTION OF PALLADIUM, PLATINUM AND RHODIUM FROM ION-CHARGED SOLUTIONS AND ITS APPLICATION TO GEOCHEMICAL-EXPLORATION TECHNIQUES USING ELECTROTHERMAL ATOMIC-ABSORPTION SPECTROMETRY [J].
BERGERON, M ;
BEAUMIER, M ;
HEBERT, A .
ANALYST, 1991, 116 (10) :1019-1024
[7]   THE DETERMINATION OF PLATINUM AND PALLADIUM IN ROCKS AND SOILS BY ELECTROTHERMAL ATOMIC-ABSORPTION SPECTROMETRY OF EXTRACTS OF THEIR IODO COMPLEXES [J].
BROOKS, RR ;
LEE, BS .
ANALYTICA CHIMICA ACTA, 1988, 204 (1-2) :333-337
[8]   Vaporization and atomization of the platinum group elements in the graphite furnace investigated by electrothermal vaporization inductively coupled plasma mass spectrometry [J].
Byrne, JP ;
Gregoire, DC ;
Benyounes, ME ;
Chakrabarti, CL .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1997, 52 (11) :1575-1586
[9]  
COOLEY ME, 1994, CANCER NURS, V17, P283
[10]   Determination of platinum group elements in impact breccias using neutron activation analysis and ultrasonic nebulization inductively coupled plasma mass spectrometry after anion exchange preconcentration [J].
Dai, XX ;
Koeberl, C ;
Fröschl, H .
ANALYTICA CHIMICA ACTA, 2001, 436 (01) :79-85