Direct Determination of the Reciprocal Lattice Spacing and the Radial Interference Distribution by the Fourier Method

1968 ◽  
Vol 12 ◽  
pp. 354-371

AbstractA procedure for extracting the interference distribution from the X-ray diffraction line using measured instrumental and wavelength distributions has been applied to the study of residual stress in copper following extension.In the direct unfolding method the principal instrumental distributions due to the source and to specimen absorption are unfolded by the Fourier method. The remaining instrumental aberrations are extracted using the centroid displacements. The resultant scattering distribution is transformed by the relations of Mitchell and de Wolff and the spectral distribution unfolded. Conditions limiting the Fourier coefficients are applied to preserve stability. Measurements have been carried out with a diffractometer equipped with a diffracted beam monochromator.The 420 and 331 interference distributions in copper following 10% extension have been compared with those of stress - free material. The distributions are symmetric both in the annealed specimen and after extension. In extension the distributions are displaced by an amount equivalent to a surface compressive stress of 6 kg/mm2, The symmetry of the interference distributions indicates that the displacement is due to a macrostress distribution.

1987 ◽  
Vol 26 (Part 1, No. 1) ◽  
pp. 157-161 ◽  
Author(s):  
Osamu Nittono ◽  
Yoshihiro Sadamoto ◽  
Sheng Kai Gong

1989 ◽  
Vol 22 (4) ◽  
pp. 363-371 ◽  
Author(s):  
R. Somashekar ◽  
I. H. Hall ◽  
P. D. Carr

Methods which determine the number and disorder of lattice planes in a crystal from the Fourier cosine coefficients of the intensity profile of an X-ray reflection use only the low harmonics and require that the coefficients be normalized so that the zero harmonic is unity. Experimentally, the profiles can only be recorded over a smaller range of scattering angle than required by the theory, and it is necessary to subtract background, which is likely to be estimated with considerable error, before determining the coefficients. It is shown that with polymer fibres this causes serious errors in the normalization, and in the values of those low harmonics used in the size and disorder determination, and prevents reliable values being obtained. Methods which avoid normalization and use only high harmonics are needed. It is shown that disorder may be obtained in such a way, but not size, for which low-order normalized coefficients are essential. A method of extrapolation is described and tested which enables the accurate high harmonics to be used to improve the estimates of the low ones. Whilst this will yield more reliable values of crystal size than are obtainable from existing methods, the accuracy depends entirely on the validity of the extrapolation, which cannot be tested in many cases of interest.


2004 ◽  
Vol 36 (1-3) ◽  
pp. 11-19 ◽  
Author(s):  
M. Sztucki ◽  
T.U. Schülli ◽  
T.H. Metzger ◽  
E. Beham ◽  
D. Schuh ◽  
...  

2004 ◽  
Vol 19 (2) ◽  
pp. 195-195
Author(s):  
A. Broadhurst ◽  
K. D. Rogers ◽  
D. W. Lane ◽  
T. W. Lowe

2005 ◽  
Vol 20 (3) ◽  
pp. 233-240
Author(s):  
A. Broadhurst ◽  
K. D. Rogers ◽  
D. W. Lane ◽  
T. W. Lowe

A direct method for determining powder diffraction data from a range of depths is described, where the linear absorption coefficient may vary with depth. A series of traditional data collections with varying angles of incidence are required, and the X-ray diffraction data arising from specific depths will be calculated by the transformation of these measured, angle-dependent spectra. These may then be analysed using any conventional method in order to gain information about characteristics of the sample in question at specific depths. Regularisation techniques have been used to solve the governing Fredholm integral equation to determine the depth-dependent diffractograms. The method has been validated by the use of simulated data having known model profiles, and has also been applied to experimental data from polycrystalline thin film samples.


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