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Comparison of X-Ray Backscatter Parameters for Complete Sample Matrix Definition*

Published online by Cambridge University Press:  06 March 2019

K.K. Niels
Affiliation:
Rogers and Associates Engineering Corporation, Salt Lake City, Utah 84107
V.C. Rogers
Affiliation:
Rogers and Associates Engineering Corporation, Salt Lake City, Utah 84107
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Equations for computing sample absorption coefficients and matrix corrections from fundamental parameters require measurement or prior knowledge of all bulk element concentrations for samples of finite thickness. Uses of these equations in commercial software have thus required either 1) “similar” standards, 2) limited applications to metal alloys, oxides or specially-prepared matrices of known composition, or 3) user supplied definitions of bulk light element concentrations. A fourth option, which provides superior analytical flexibility, is the use of backscattered x-ray intensities with element scatter cross-sections to define the unmeasured light-element component of the sample matrix. Backscatter intensities constitute the only spectral basis for routinely characterizing the light-element component of geological, biological and other materials which contain significant H, C, N, O, etc. They thus offer a unique basis for utilizing fundamental-parameter matrix corrections in the general case of unknown samples without standards.

Type
VII. Mathematical Models and Computer Applications in XRF
Copyright
Copyright © International Centre for Diffraction Data 1983

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Footnotes

*

Supported by National Science Foundation Grant CHE-8260151.

References

1. Shiraiwa, T. and Fujino, N., “Theoretical Calculations of Fluorescent X-ray Intensities in Fluorescent X-ray Spectrochemical Analysis,” Japan J. Appl. Phys., 5, 886–2, 1966.Google Scholar
2. Sparks, C.J., “Quantitative X-ray Fluorescence Analysis Using Fundamental Parameters,” Advan. In X-ray Anal., 19, 1952, 1976.Google Scholar
3. Andermann, G. and Kemp, J.W., “Scattered X-rays as Internal Standards in X-ray Emission Spectroscopy,” Anal. Chem., 30, 1306–29, 1958.Google Scholar
4. Reynolds, R.C., “Matrix Corrections in Trace Element Analysis by X-ray Fluorescence:Estimation of the Mass Absorption Coefficient by Compton Scattering,” Am. Mineral., 48, 1133–23, 1963.Google Scholar
5. Reynolds, R.C., “Estimation of Mass Absorption Coefficients by Compton Scattering:Improvements and Extensions of the Method,” Am. Mineral., 52, 1493–22, 1967.Google Scholar
6. Franzini, M., Leoni, L. and Saitta, M., “Determination of the X-ray Mass Absorption Coefficient by Measurement of the Intensity of AgKα Compton Scattered Radiation,” X-ray Spectrom., 5, 8487, 1976.Google Scholar
7. Feather, C.E. and Willis, J.P., “A Simple Method for Background and Matrix Correction of Spectral Peaks in Trace Element Determination by X-ray Fluorescence Spectrometry,” X-ray Spectrom., 5, 4148, 1976.Google Scholar
8. Leoni, L. and Saitta, M., “Matrix Effect Corrections by AgKα Compton Scattered Radiation in the Analysis of Rock Samples for Trace Elements,” X-ray Spectrom., 6, 181–2, 1977.Google Scholar
9. Giauque, R.D., Garrett, R.B. and Goda, L.Y., “Determination of Trace Elements in Light Element Matrices by X-ray Fluorescence Spectrometry with Incoherent Scattered Radiation as an Internal Standard,” Anal. Chem., 51, 511–2, 1979.Google Scholar
10. Nielson, K.K., “Matrix Corrections for Energy Dispersive X-ray Fluorescence Analysis of Environmental Samples with Coherent/ Incoherent Scattered X-rays,” Anal. Chem., 49, 641–2, 1977.Google Scholar
11. Nielson, K.K., “SAP3:A Computer Program for X-ray Fluorescence Data Reduction for Environmental Samples,“ Richland, WA:Battelle Pacific Northwest Laboratory Report BNWL-2193, 1977.Google Scholar
12. Van Espen, P., Vant dack, L., Adams, F. and Van Grieken, R., “Effective Sample Weight from Scatter Peaks in Energy Dispersive X-ray Fluorescence,” Anal. Chem., 51, 961–2, 1979.Google Scholar
13. Nielson, K.K. and Sanders, R.W., “X-ray Fluorescence Analysis of Environmental and Geological Materials,” Trans. Am. Nucl. Soc. 39, 6061, 1981.Google Scholar
14. Nielson, K.K. and Sanders, R.W., “Multielement Analysis of Unweighed Biological and Geological Samples Using Backscatter and Fundamental Parameters,” Advan. In X-ray Anal., 2 6, 385–2, 1983.Google Scholar
15. Nielson, K.K. and Sanders, R.W., The SAP3 Computer Program For Quantitative Multielement Analysis by Energy Dispersive X-ray Fluorescence,” Richland, WA:Battelle Pacific Northwest Laboratory Report PNL-4173, 1982.Google Scholar
16. McMaster, W.H., Del Grande, N.K., Mallett, J.H. and Hubbell, J.H., “Compilation of X-ray Cross Sections,” Univ. of California, Report UCRL-50174, Sec. II, Rev. 1, 1969.Google Scholar