An Apparatus for Producing Powder‐Like X‐Ray Diffraction Patterns from Single Crystals

1949 ◽  
Vol 20 (5) ◽  
pp. 365-366 ◽  
Author(s):  
F. W. Matthews ◽  
A. O. McIntosh
1978 ◽  
Vol 33 (8) ◽  
pp. 918-923 ◽  
Author(s):  
F. Müller ◽  
E. Schulte

Flash-x-ray-diffraction patterns (FXD) with an exposure time of 4 ns of NaCl single crystals compressed by plane shock waves are obtained at pressures of about 30 kbar. From the diffraction patterns the compression is determined and compared with Hugoniot data. During shock load the lattice shows an uniaxial compression. While in case of measurements at the free surface an observation time of only a few nanoseconds is available, this experimental set-up allows an observation time of two microseconds.


Author(s):  
H. Brigitte Krause ◽  
Donald L. Gibbon

AbstractSelected-area electron-diffraction patterns and x-ray diffraction powder patterns were taken of crushed single crystals of Pb


1997 ◽  
Vol 12 (9) ◽  
pp. 2274-2280 ◽  
Author(s):  
B. Zhang ◽  
M. Estermann ◽  
W. Steurer

Decaprismatic single crystals taken from a series of alloys of nominal compositions within Al65–77Co3–22Ni3–22 have been studied by means of x-ray diffraction techniques. The substitution of Co by Ni in increasing amounts changes the (pseudo)decagonal diffraction patterns drastically and indicates structural changes which range from a single-crystalline approximant via orientationally ordered nanodomain structures and quasiperiodic phases with different types of ordering phenomena, to a basic decagonal phase. A quantum phase diagram analysis shows a clear separation of the stability regions of the ternary systems described in this study and other decagonal phases.


1994 ◽  
Vol 1 (1) ◽  
pp. 11-12 ◽  
Author(s):  
Keliang Liu ◽  
H. Todd Miles ◽  
Kevin D. Parris ◽  
V. Sasisekharan

1957 ◽  
Vol 35 (1) ◽  
pp. 38-47 ◽  
Author(s):  
G. B. Craig ◽  
B. Chalmers

The tensile plastic deformation of single-crystal and tricrystal specimens of zinc was investigated by analysis of the external change in shape of the specimens, and of the changes in X-ray diffraction patterns. It was demonstrated that the single crystals deformed by slip on the basal plane, but pyramidal as well as basal slip occurred in specimens containing grain boundaries.


2015 ◽  
Vol 48 (4) ◽  
pp. 1342-1345 ◽  
Author(s):  
William Whitley ◽  
Chris Stock ◽  
Andrew D. Huxley

Although CCD X-ray detectors can be faster to use, their large-area versions can be much more expensive than similarly sized photographic plate detectors. When indexing X-ray diffraction patterns, large-area detectors can prove very advantageous as they provide more spots, which makes fitting an orientation easier. On the other hand, when looking for single crystals in a polycrystalline sample, the speed of CCD detectors is more useful. A new setup is described here which overcomes some of the limitations of limited-range CCD detectors to make them more useful for indexing, whilst at the same time making it much quicker to find single crystals within a larger polycrystalline structure. This was done by combining a CCD detector with a six-axis goniometer, allowing the compilation of images from different angles into a wide-angled image. Automated scans along the sample were coupled with image processing techniques to produce grain maps, which can then be used to provide a strategy to extract single crystals from a polycrystal.


Single crystals of naturally occurring graphite which had been treated with bromine vapour have been examined by electron and X-ray diffraction and also by electron microscopy. The intercalated bromine is in the form of layers, interleaved between the graphite layers in a sequence which is dependent upon the concentration of bromine. The structure within a bromine layer is relatively highly ordered and has been shown to take on two forms, one which occurs at concentrations in excess of 47 (wt.) %, the other occurs at lower concentrations. Detailed analysis of the diffraction patterns given by the lower concentration form suggest that it is composed of chains of Br 2 molecules, in which the interatomic distances are virtually identical with those of solid bromine.


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