Deconvolution of instrument andKα2contributions from X-ray powder diffraction patterns using nonlinear least squares with penalties

2018 ◽  
Vol 51 (1) ◽  
pp. 112-123 ◽  
Author(s):  
Alan A. Coelho

A new deconvolution method, tolerant of noise and independent of knowing the number of Bragg peaks present, has been developed to deconvolute instrument and emission profile distortions from laboratory X-ray powder diffraction patterns. Removing these distortions produces higher-resolution patterns from which the existence of peaks and their shapes can be better determined. Deconvolution typically comprises the use of the convolution theorem to generate a single aberration from instrument and emission profile aberrations and then the Stokes method to deconvolute the resulting aberration from the measured data. These Fourier techniques become difficult when the instrument function changes with diffraction angle and when the signal-to-noise ratio is low. Instead of Fourier techniques, the present approach uses nonlinear least squares incorporating penalty functions, as implemented in the computer programTOPAS-Academic. Specifically, diffraction peaks are laid down at each data point with peak shapes corresponding to either expected peak shapes or peak shapes narrower than expected; a background function is included. Peak intensities and background parameters are then adjusted to obtain the best fit to the diffraction pattern. Rietveld refinement of the deconvoluted pattern results in background parameters that are near identical to those obtained from Rietveld refinement of the original pattern. Critical to the success of the deconvolution procedure are two penalty functions, one a function of the background parameters and the other a function of the peak intensities. Also of importance is the use of a conjugate gradient solution method for solving the matrix equationAx=b.

1983 ◽  
Vol 27 ◽  
pp. 75-80
Author(s):  
W. Parrish ◽  
T. C. Huang ◽  
G. L. Ayers

AbstractA method for computer simulation of X-ray powder diffraction patterns which are identical to those obtained experimentally is described. The calculated pattern is generated directly from the d's (or 2θs) and intensities of the phase(s) and is based on a profile fitting algorithm which uses the instrument function to form the profile shapes at all reflection angles. Examples of simulated patterns of mixtures, line broadening, linear and amorphous backgrounds, and counting noise are given.


Author(s):  
J. Nolan ◽  
A. D. Edgar

SummaryAn X-ray investigation has been made of synthetic pyroxenes in the system acmite-diopside, crystallized at 750° C and 1000 kg/cm2 water-vapour pressure. Lattice parameters of these pyroxenes have been determined by least squares analyses of powder diffraction patterns and show an approximately linear relationship with composition, plotted as weight per cent. A rapid X-ray method has also been devised for the determination of the compositions of pyroxenes of this series.


1999 ◽  
Vol 14 (3) ◽  
pp. 181-189 ◽  
Author(s):  
W. Wong-Ng ◽  
J. A. Kaduk ◽  
R. A. Young ◽  
F. Jiang ◽  
L. J. Swartzendruber ◽  
...  

The structures of the solid solution series (Sr4−δCaδ)PtO6, with δ=0, 0.85(1), 2, and 3, have been investigated using the Rietveld refinement technique with laboratory X-ray powder diffraction data. A complete solid solution between Sr and Ca was confirmed to exist. These compounds crystallize in the rhombohedral space group R3¯c. The cell parameters of the series range from a of 9.4780(3) to 9.7477(1) Å, and c from 11.3301(4) to 11.8791(1) Å for δ from 3 to 0, respectively. The structure consists of chains of alternating trigonal prismatic (Sr, Ca)O6 and octahedral PtO6 units running parallel to the c axis. These chains are connected to each other via a second type of (Sr, Ca) ions, which are surrounded by eight oxygens, in a distorted square antiprismatic geometry. As Ca replaced Sr in Sr4PtO6, it was found to substitute preferentially in the smaller octahedral (Sr, Ca)1 site (6a) rather than at the eight-coordinate (Sr, Ca)2 site (18e). There appears to be an anomaly of cell parameters a and c at the compound Sr3.15Ca0.85PtO6. Their dependence on Ca content changes at δ≈1.00, where the Ca has fully replaced Sr in the 6a site. The substitution of Sr by Ca reduced the average (Sr, Ca)1–O length from 2.411 to 2.311 Å and (Sr, Ca)2–O from 2.659 to 2.570 Å as the composition varied from Sr4PtO6 to SrCa3PtO6. Reference X-ray powder diffraction patterns were prepared from the Rietveld refinement results for these members of the solid solution series. Magnetic susceptibility measurements of three of the samples (δ=0, 0.85, 2) show electronic transitions at low temperatures.


2013 ◽  
Vol 29 (1) ◽  
pp. 28-32 ◽  
Author(s):  
Ana Palčić ◽  
Ivan Halasz ◽  
Josip Bronić

The crystal structure of copper(ii) citrate monohydrate (C6H4O7Cu2·H2O) has been solved from a mixture powder diffraction pattern. Approach to indexing, structure solution and Rietveld refinement of multiphase diffraction patterns is discussed. Rietveld refinement is carried out employing free-atom refinement and rigid body refinement.


1999 ◽  
Vol 32 (2) ◽  
pp. 168-173 ◽  
Author(s):  
C. Dong ◽  
H. Chen ◽  
F. Wu

This paper presents a new algorithm to remove the CuKα2profile in X-ray powder diffraction patterns. Previous algorithms for α2elimination can be divided into two categories. The first category assumes the shape identity of the α1and α2components. The second category uses parameters by fitting experimental data. The first category is not accurate and the second one is instrument-dependent. The algorithm presented here uses the CuKα emission profile obtained from monolithic double-crystal measurements. Therefore, it is more accurate and less instrument-dependent than the previous methods. This algorithm has been tested and applied in software for diffraction data processing. The present method can be extended to removeKα2lines of other radiations.


2002 ◽  
Vol 35 (5) ◽  
pp. 634-636 ◽  
Author(s):  
Z. K. Heiba ◽  
Karimat El-Sayed

Structural and thermal expansion studies of Li2ZrO3were carried out by recording X-ray powder diffraction patterns at five temperatures, 82, 198, 300, 423 and 573 K. The Rietveld refinement method was used for the analysis. There were large anisotropic changes in the lattice parameters as a function of temperature, slight changes in the fractional coordinates of the different atoms, and anisotropic changes in the interatomic distances between the different cations. The correlation of these anisotropies with the structure is considered.


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