1998
DOI: 10.1039/a804110e
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Solid sampling electrothermal atomic absorption spectrometry for analysis of aluminium oxide powders

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Cited by 34 publications
(17 citation statements)
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“…In this circumstance, it is important to consider the lifetime of the graphite parts. Typically, the analysis of relatively large amounts of samples with high Al 2 O 3 and/or high SiO 2 contents leads to the rapid deterioration of the graphite platforms owing to their interaction with graphite (C reduces these species) [33][34][35]. Therefore, and taking also into account the expected level of the analytes, selecting small sample aliquots (0.05 to 0.20 mg) seems preferable.…”
Section: Optimization Of the Working Conditions For The Analysis Of Tmentioning
confidence: 97%
“…In this circumstance, it is important to consider the lifetime of the graphite parts. Typically, the analysis of relatively large amounts of samples with high Al 2 O 3 and/or high SiO 2 contents leads to the rapid deterioration of the graphite platforms owing to their interaction with graphite (C reduces these species) [33][34][35]. Therefore, and taking also into account the expected level of the analytes, selecting small sample aliquots (0.05 to 0.20 mg) seems preferable.…”
Section: Optimization Of the Working Conditions For The Analysis Of Tmentioning
confidence: 97%
“…Due to its unique physical and chemical characteristics, tantalum pentaoxide (Ta 2 O 5 ) has become an important material in the electrical, mechanical, steel, optical, aviation, and semiconductor industries (1,2). It should be pointed out that the growing application of advanced materials in high-tech fields enhances the demand for strictly controlled properties which are often directly correlated to the concentrations of trace impurities (3)(4)(5)(6). Therefore, a powerful, rapid, and reliable analytical method is required for the elemental characterization of impurities at trace and ultra-trace levels in Ta 2 O 5 .…”
Section: Introductionmentioning
confidence: 99%
“…When focusing on SS-GFAAS, it can be pointed out that while during the 1980s many calibration approaches were evaluated (including the use of certified reference materials, 9,10 home-made solid standards 11 and different standard addition approaches 12,13 ), in later years most of the recent papers have reported satisfactory results using external calibration with aqueous standards. 2,[14][15][16] This is owing to the generalized use of peak area integration as the measurement mode, the advances in instrumentation and the potential of chemical modification.…”
Section: Introductionmentioning
confidence: 99%