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Noninvasive Quantitative Chromium(III) Speciation in Neat Solid Mixtures by Extended X-ray Absorption Fine Structure Spectroscopy

Marc M. Lamoureux, J. Craig. Hutton, David L. Styris, Richard Gordon

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Abstract

A procedure that uses extended X-ray absorption fine structure (EXAFS) spectroscopy for quantitative chromium(III) speciation in neat solid mixtures is described. The procedure uses the full, filtered EXAFS, e.g., 4 ≤ k ≤ 12 Å −1 , rather than the smaller k-range associated with a single coordination sphere. Concentration is determined by a simple correlation of full, filtered EXAFS of standards with full, filtered EXAFS of mixtures. Under optimized conditions, calibration curves for mixtures of Cr 2 O 3 and Cr(NO 3 ) 3 ·9H 2 O have slopes of 1.002, respective intercepts of −0.7% and 0.5%, and correlation coefficients of 0.9991. Fluorescence EXAFS from mixtures must be compared to fluorescence EXAFS from standards, and the matrices and thicknesses of standards and mixtures must be closely matched. Transmission EXAFS of standards must be obtained to correct for self-absorption effects.

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What this paper is about

A procedure that uses extended X-ray absorption fine structure (EXAFS) spectroscopy for quantitative chromium(III) speciation in neat solid mixtures is described. The procedure uses the full, filtered EXAFS, e.g., 4 ≤ k ≤ 12 Å −1 , rather than the smaller k-range associated with a single coordination sphere. Concentration is determined by a simple correlation of full, filtered EXAFS of standards with full, filtered EXAFS of mixtures. Under optimized conditions, calibration curves for mixtures of Cr 2 O 3 and Cr(NO 3 ) 3 ·9H 2 O have slopes of 1.002, respective intercepts of −0.7% and 0.5%, and correlation coefficients of 0.9991. Fluorescence EXAFS from mixtures must be compared to fluorescence EXAFS from standards, and the matrices and thicknesses of standards and mixtures must be closely matched. Transmission EXAFS of standards must be obtained to correct for self-absorption effects.

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Available abstract

A procedure that uses extended X-ray absorption fine structure (EXAFS) spectroscopy for quantitative chromium(III) speciation in neat solid mixtures is described. The procedure uses the full, filtered EXAFS, e.g., 4 ≤ k ≤ 12 Å −1 , rather than the smaller k-range associated with a single coordination sphere. Concentration is determined by a simple correlation of full, filtered EXAFS of standards with full, filtered EXAFS of mixtures. Under optimized conditions, calibration curves for mixtures of Cr 2 O 3 and Cr(NO 3 ) 3 ·9H 2 O have slopes of 1.002, respective intercepts of −0.7% and 0.5%, and correlation coefficients of 0.9991. Fluorescence EXAFS from mixtures must be compared to fluorescence EXAFS from standards, and the matrices and thicknesses of standards and mixtures must be closely matched. Transmission EXAFS of standards must be obtained to correct for self-absorption effects.

Key concepts: Extended X-ray absorption fine structure, Absorption (acoustics), Chemistry, Analytical Chemistry (journal), Spectroscopy, Surface-extended X-ray absorption fine structure, Chromium, Absorption spectroscopy

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