Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-26T22:27:17.486Z Has data issue: false hasContentIssue false

Chemical Bonding Studies of Solutions by High Resolution X-ray Fluorescence Spectroscopy

Published online by Cambridge University Press:  06 March 2019

Tom Scimeca
Affiliation:
University of Tokyo Hongo, Bunkyo, Tokyo 113, Japan
Sei Fukushima
Affiliation:
University of Tokyo Hongo, Bunkyo, Tokyo 113, Japan
Kazuo Miyamura
Affiliation:
University of Tokyo Hongo, Bunkyo, Tokyo 113, Japan
Yohichi Gohshi
Affiliation:
University of Tokyo Hongo, Bunkyo, Tokyo 113, Japan
Get access

Extract

High resolution X-Ray Fluorescence Spectroscopy(HRXRFS) has been extensively used as a chemical bonding probe for both solids and gases for quite some time. However there have been virtually no HRXRFS studies reported on liquid phase systems and particularly on solution systems. This seems somewhat surprising not only because this is an unexplored area, but because much of chemistry and chemical bonding occurs in solution. Furthermore, since HRXRFS is a “photon in - photon out” technique, providing one uses relatively energetic x-rays, the experimental techniques for performing these types of measurements are relatively straightforward, especially when compared to techniques which utilize charged particles.

Type
III. Long-Wavelength X-Ray Spectrometry
Copyright
Copyright © International Centre for Diffraction Data 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. See for example, Meisel, A., Leonhardt, G. and Szargan, R., “X-Ray Spectra and Chemical Binding“; Springer Series in Chemical Physics 37, Springer-Verlag, Berlin 1989.Google Scholar
2. Andermann, G. and Whitehead, H. C., Adv. in X-Ray Anal. 14, 453 (1971).Google Scholar
3. Siegbahn, H., J. Phys. Chem. 89, 897 (1985).Google Scholar
4. Gohshi, Y., Kamada, H., Kohra, K., Utaka, T. and Arai, T., Appl. Spec. 36(2), 171(1982).Google Scholar
5. The cell used was manufactured by Rigaku Instruments.Google Scholar
6. Savitzky, A. and Golay, M. J. E., Anal. Chem. 36(8), 1627(1964).Google Scholar
7. Narlen, A. H., Vaslow, F., Levy, H. A., J. Chem. Phys. 58(11), 5017(1973).Google Scholar
8. Jansen, H. J. F. and Freeman, A. J., Phys. Rev B 33(12), 8629(1986).Google Scholar
9. Adachi, H., Tsukada, M. and Satoko, C., J. Phys. Soc. Jpn. 42, 875 (1978). Self exchange parameters of 0.7 were used, except for calculations involving hydrogen, in which case values were taken from K. Schwartz, Phys. Rev., B5, 2466 (1972).Google Scholar
10. Deslattes, R., Phys. Rev. 133, A390(1064);133, A399(1964).Google Scholar
11. Deslattes, R. D., LaVilla, R. E., Cowan, P. L. and Renins, A., Phys. Rev. A 27(2), 923(1982).Google Scholar
12. Aberg, T., Phys. Rev. 156, 35 (1967).Google Scholar
13. Kawai, J., Satoko, C. and Gohshi, Y., Spec. Acta 42B(6), 745(1987).Google Scholar
14. Kawai, J., Satoko, C., Fujisawa, K. and Gohshi, Y., Phys. Rev. Lett. 57(8), 988(1986).Google Scholar
15. Saturation concentrations were taken from CRC Handbook of Chemistry.Google Scholar
16. Lagarde, P., Fontaine, A., Raoux, D., Sadoc, A., and Migliardo, P., J. Chem. Phys. 72(5), 3061(1980).Google Scholar
17. Magini, M. and Radnai, T., J. Chem. Phys. 71(11), 4255(1979).Google Scholar
18. Matsubara, E. and Waseda, Y., J. Phys. : Condens. Matter 1, 8575 (1989).Google Scholar
19. Fontana, M. P., Maisano, G., Migfiardo, P. and Wanderlingh, F., Solid State Communications 23, 489 (1977).Google Scholar
20. Maisano, G., Migliardo, P., Wanderlingh, F., Fontana, M. P., 68(12), 5594(1978).Google Scholar
21. Miyamura, K., Ban, H., Kamide, S., Kawase, A. and Gohshi, Y., To be submitted shortly.Google Scholar
22. Sugiura, C., J. Phys. Soc. Japan 33(2), 455(1971).Google Scholar