Vaporization and removal of silica for the direct analysis of geological materials by slurry sampling electrothermal vaporization-inductively coupled plasma-mass spectrometry

被引:23
作者
Ben Younes, ME
Grégoire, DC
Chakrabarti, CL
机构
[1] Geol Survey Canada, Ottawa, ON K1A 0E8, Canada
[2] Carleton Univ, Ottawa Carleton Chem Inst, Dept Chem, Ottawa, ON K1S 5B6, Canada
关键词
D O I
10.1039/a903269j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Reported is a method for the removal of silica for the direct analysis of solid geological samples high in silica content using slurry sampling electrothermal vaporization-inductively coupled plasma-mass spectrometry (ETV-ICP-MS). The ETV-ICP-MS vaporization curve for SiO2, sampled as a slurry, is reported for temperatures ranging from 810-2600 degrees C. This curve showed that silica was completely vaporized at a temperature of 2200 degrees C. The effect of using HF as a chemical modifier to remove silica as the tetrafluoride was studied. It was found that HF could completely remove any Si attributed to silica if sufficient modifier were added and an adequate reaction time allowed. At reaction hold times that were less than optimal, two Si signals were observed. The first signal, which appears at an earlier time and at a temperature less than 480 degrees C, is attributed to the volatilization of silicon tetrafluoride. The second signal, which appears at a later time and at a temperature of about 2500 degrees C, is attributed to the vaporization of residual unreacted SiO2 remaining in the graphite tube, or to the vaporization of a mixture of SiO2 and SiC. 20 mu l of 50% HF is effective in completely removing 0.125 mu g of SiO2. No adverse effects including corrosive degradation of the graphite tube were observed over the lifetime of the tube, which exceeded 200 firings. Hydrofluoric acid chemical modifier was successful in removing virtually all the silica content in natural silicate standard reference materials.
引用
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页码:1703 / 1708
页数:6
相关论文
共 31 条
[1]  
ALLARY J, 1995, APPL SPECTROSC, V49, P1796
[2]   METAL EXTRACTION BY HYDROFLUORIC-ACID FROM SLURRIES OF GLASS MATERIALS IN GRAPHITE-FURNACE ATOMIC-ABSORPTION SPECTROMETRY [J].
BENDICHO, C ;
DELOOSVOLLEBREGT, MTC .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1990, 45 (07) :695-710
[3]   THE INFLUENCE OF PYROLYSIS AND MATRIX MODIFIERS FOR ANALYSIS OF GLASS MATERIALS BY GFAAS USING SLURRY SAMPLE INTRODUCTION [J].
BENDICHO, C ;
DELOOSVOLLEBREGT, MTC .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1990, 45 (07) :679-693
[4]   SOLID SAMPLING IN ELECTROTHERMAL ATOMIC-ABSORPTION SPECTROMETRY USING COMMERCIAL ATOMIZERS - A REVIEW [J].
BENDICHO, C ;
DELOOSVOLLEBREGT, MTC .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1991, 6 (05) :353-374
[5]  
EAMS JC, 1980, ANAL CHEM, V52, P1248
[6]  
FONESCA RW, 1995, APPL SPECTROSC, V49, P1403
[7]   Effect of oxygen ashing on analyte transport efficiency using ETV-ICP-MS [J].
Fonseca, RW ;
Miller-Ihli, NJ ;
Sparks, C ;
Holcombe, JA ;
Shaver, B .
APPLIED SPECTROSCOPY, 1997, 51 (12) :1800-1806
[8]   Influence of sample matrix components on the selection of calibration strategies in electrothermal vaporization inductively coupled plasma mass spectrometry [J].
Fonseca, RW ;
MillerIhli, NJ .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1996, 51 (13) :1591-1599
[9]   Mechanism of vaporization of yttrium and rare earth elements in electrothermal vaporization inductively coupled plasma mass spectrometry [J].
Goltz, DM ;
Gregoire, DC ;
Chakrabarti, CL .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1995, 50 (11) :1365-1382
[10]   DIRECT ANALYSIS OF SOLIDS BY ULTRASONIC SLURRY ELECTROTHERMAL VAPORIZATION INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY [J].
GREGOIRE, DC ;
MILLERIHLI, NJ ;
STURGEON, RE .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1994, 9 (05) :605-610