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Determination of indium in geological materials by electrothermal-atomization atomic absorption spectrometry with a tungsten-impregnated graphite furance

January 1, 1984

The sample is fused with lithium metaborate and the melt is dissolved in 15% (v/v) hydrobromic acid. Iron(III) is reduced with ascorbic acid to avoid its coextraction with indium as the bromide into methyl isobutyl ketone. Impregnation of the graphite furnace with sodium tungstate, and the presence of lithium metaborate and ascorbic acid in the reaction medium improve the sensitivity and precision. The limits of determination are 0.025–16 mg kg−1 indium in the sample. For 22 geological reference samples containing more than 0.1 mg kg−1 indium, relative standard deviations ranged from 3.0 to 8.5% (average 5.7%). Recoveries of indium added to various samples ranged from 96.7 to 105.6% (average 100.2%).

Publication Year 1984
Title Determination of indium in geological materials by electrothermal-atomization atomic absorption spectrometry with a tungsten-impregnated graphite furance
DOI 10.1016/S0003-2670(00)85809-2
Authors L. Zhou, T. T. Chao, A. L. Meier
Publication Type Article
Publication Subtype Journal Article
Series Title Analytica Chimica Acta
Index ID 70012668
Record Source USGS Publications Warehouse
USGS Organization Denver Federal Center