Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-02T22:24:16.451Z Has data issue: false hasContentIssue false
  • English
  • Français

A Comparison of Methods for Reducing Preferred Orientation‡

Published online by Cambridge University Press:  06 March 2019

L. D. Calvert ,
A. F. Sirianni ,
G. J. Gainsford  and
C. R. Hubbard
L. D. Calvert
Affiliation:
Chemistry Division, National Research Council of Canada, Ottawa, K1A0R9, CANADA
A. F. Sirianni
Affiliation:
Chemistry Division, National Research Council of Canada, Ottawa, K1A0R9, CANADA
G. J. Gainsford
Affiliation:
Chemistry Division, National Research Council of Canada, Ottawa, K1A0R9, CANADA
C. R. Hubbard
Affiliation:
Center for Materials Science, National Bureau of Standards, Washington, D.C, 20234
Get access

Extract

Preferred orientations in powder diffraction specimens can cause large errors in measured intensities. An extreme case is shown in Figure 1, Smith and Barrett (1979) reviewed the various methods which have been proposed for reducing this effect. Subsequently, two methods which are used commercially for aggregating finely divided solids have been proposed for preparing powder diffraction specimens (Smith, Snyder, and Brownell, 1979; Calvert and Sirianni, 1980). In one of these, spray drying, a finely divided solid is suspended in a liquid together with small quantities of a deflocculent and a binder. This mixture is pulled by venturi action through a nozzle into a heated chamber. The spherically shaped aggregates dry before falling to a collection surface. The apparatus is fairly large (3 X 3 X 4 ft. at NBS), and operating parameters must be carefully chosen.

Type
III. Quantitative XRD Analysis
Information
Advances in X-Ray Analysis , Volume 26: Thirty-First Annual Conference on Applications of X-ray Analysis, August 1-6, 1982 , 1982 , pp. 105 - 110
Copyright
Copyright © International Centre for Diffraction Data 1982

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.)

Footnotes

*

Permanent address: D.S.I.R., Petone, New Zealand.

‡

Contribution of the National Bureau of Standards; not subject to copyright.

References

Calvert, L. D. and Sirianni, A. F., 1980, J. Appl. Cryst., 13:462.Google Scholar
Kihlborg, L., 1963, Ark. Keini., 21:357–63.Google Scholar
McCauley, J. W., Newnham, R. E., and Gibbs, G. V., 1973, Amer. Miner., 58:249–54Google Scholar
NBS Monograp. 25, Section 18, 1981.Google Scholar
Morris, M. C., McMurdie, H. F., Evans, E. H., Paretzkin, B., Parker, H. S., Panagiotopoulos, N. C., and Hubbard, C. R., p. 3–4, National Bureau of Standards, Washington, D.C. 20234.Google Scholar
Smith, D. K. and Barrett, C. S., 1979, Adv. X-Ray. Analy., 22:1.Google Scholar
Smith, S. T., Snyder, R. L., and Brownell, W. E., 1979, Adv. X-Ray Analy., 22:77.Google Scholar