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Polymer Films as Calibration Standards for X-ray Fluorescence Analysis

Published online by Cambridge University Press:  06 March 2019

T. G. Dzubay
Affiliation:
U . S. Environmental Protection Agency Environmental Sciences Research Laboratory Research Triangle Park, WC 27711
P. J. Lamothe
Affiliation:
U . S. Environmental Protection Agency Environmental Sciences Research Laboratory Research Triangle Park, WC 27711
H. Yasuda
Affiliation:
Polymer Research Laboratory Research Triangle Institute Research Triangle Park, NC 27709
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Abstract

A new type of calibration standard has been developed for X-ray fluorescence analysis of thin samples. Each standard consists of a polymer film containing a single calibration element. The film is cast from a homogeneous solution containing known amounts of an organometallic compound and a polymer. Polymers of cellulose acetate-propionate and polystyrene are used because of their low moisture affinity. The films have a low (2-4 mg/cm2) mass per unit area for minimal X-ray attenuation. Standards of V, Co, Hi, and Pb have been successfully made. Typical concentrations of 20 μg/cm2 yield excellent spectra with a low background. The method shows promise for making standards of additional elements.

Type
X-Ray Fluorescence
Copyright
Copyright © International Centre for Diffraction Data 1976

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References

1. Pradzynski, A. H. and Rhodes, J. R., “Development of Synthetic Standard Samples for Trace Analysis of Air Particulates Publication 598, p.320336, American Society for Testing and Materials (1976).Google Scholar
2. Camp, D. C., VanLehn, A. L., Rhodes, J. R., and Pradzynski, A. H., “Intercomparison of Trace Element Determinations in Simulated and Real Air Particulate Samples,” X-Ray Spectrom. 4, 123137 (1975).Google Scholar
3. Baum, R. M., Gutknecht, W. F., Willis, R. D., and Walter, R. L., “Preparation of Standard Targets for X-Ray Analysis,” Anal. Chem. 47, 1727-1728 (1975).Google Scholar
4. Stiles, A. R., Dzubay, T. G., Baum, R. M., Walter, R. L., Willis, R. D., Moore, L. J., Garner, E. L., Gramlich, J. W., and Machlan, L. A., “Calibration of an Energy Dispersive X-Ray Fluorescence Spectrometer,” in Gould, R. W., Barrett, C. S., Newkirk, J. B., and Ruud, C. O., Editors, Advances in X-Ray Analysis Vol. 19, p.473 486, Kendall/Hunt (1976).Google Scholar
5. Giauque, R. D., Garrett, R. B., and Goda, L. Y., “Calibration of Energy Dispersive X-Ray Spectrometers for Analysis of Thin Environmental Samples,” in X-Ray Fluorescence Methods for Analysis of Environmental Samples, Chapter 11, Ann Arbor Science (1976).Google Scholar
6. Jaklevic, J. M., Goulding, F. S., Jarett, B. V., and Meng, J. D., “Applications of X-Ray Fluorescence Techniques to Measure Elemental Composition of the Atmosphere,” in Stevens, R. K. and Herget, W. Y., Editors, Analytical Methods Applied to Air Pollution Measurements p.123146, Ann Arbor Science (1974).Google Scholar