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Determination of impurities in high-purity niobium(V) oxide by high-resolution continuum source graphite furnace atomic absorption spectrometry after sorption preconcentration
Authors:V V Eskina  O A Dalnova  E N Kareva  V B Baranovskaya  Yu A Karpov
Institution:1.State Research and Design Institute of Rare-Metal Industry “Giredmet”,Moscow,Russia;2.National University of Science and Technology “MISiS”,Moscow,Russia;3.Kurnakov Institute of General and Inorganic Chemistry,Russian Academy of Sciences,Moscow,Russia
Abstract:Method of sorption–atomic-absorption determination of Co, Cr, Cu, Fe, Mn, and Ni in samples of high-purity Nb2O5 with heterochain S,N-containing sorbents was developed. The method is based on the sorption preconcentration of trace impurities followed by their determination by high-resolution continuum source graphite furnace atomic absorption spectrometry (HR CS GFAAS). Selectivity of three original inhouse synthesized S,N-containing heterochain sorbents was studied. The recoveries of Co, Cr, Cu, Fe, Mn, and Ni using heterochain sorbents OKS, MTH, and GLSH were 100, 80, and 76%, correspondingly. Sorbent “OKS”, which provided the quantitative recovery of trace impurities, was chosen for further research. The sorption conditions for chloride solutions of different acidities (0.1–3 M HCl) were studied and optimized. Using the conditions established for the sorption and HR CS GFAAS analysis, trace Co, Cr, Cu, Fe, Mn, and Ni were determined in high purity Nb2O5 with a relative error less than 5%. The trueness control of the obtained results is confirmed by the “added–found” method. The developed method allows us to determine concentrations of analytes: 0.02–0.20 ppm Co, 2.0–3.3 ppm Cr, 0.2–1.5 ppm Cu, 6.0–21.0 ppm Fe, 0.6–0.8 ppm Mn, and 2.8–3.5 ppm Ni. The proposed methodology can be successfully extended to the determination of various trace elements in other high-purity inorganic materials.
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