Preparation of Samples for the XRD Analysis
Proper sample preparation is one of the most important requirements in the analysis of powder samples by X-ray diffraction. This statement is especially true for soils and clays that contain finely divided colloids, which are poor reflectors of x-rays, as well as other types of materials such as iron oxide coatings and organic materials that make characterization by XRD more difficult. Sample preparation includes not only the right sample treatments to remove undesirable substances, but also appropriate techniques to obtain desirable particle size, orientation, thickness, etc.
Important Factors in Sample Preparation
1. Sample properties also influence the quality of a powder pattern by either reducing intensities or distorting intensities.
2. Preferred orientation or texture: By texture we mean that the powder particles do not have an arbitrary shape but a strongly regular anisotropic shape, typically platelets or needles. On preparation these are then preferably oriented along the sample surface massively changing the peak intensities. Several techniques may be employed to minimize this effect.
· The most efficient way is to form a slurry in a highly viscous liquid such as nail varnish. In such a liquid, the random orientation is retained on drying.
· Alternatively, the anisotropic particle shape can be reduced by grinding in a ball mill. This should be done with great care as excessive grinding can easily break down the particle size to the nanometer size and lead to amorphisation. It is recommended to try the effect of subsequent 5 minute grinding intervals to optimize the process on respective samples. In the case of coatings or thin films preferred orientation is often a desired effect. In this case Rietveld refinement can be used to determine the degree of texture.
3. Crystallite size and strain: The broadness of a diffraction peak corresponds to the mean crystallite size in a reciprocal manner. The smaller the average crystallite size, the broader the reflections and the lower the absolute intensities. This effect becomes visible below and average crystallite size of less than 200 nm. Related to crystallite size broadening is strain broadening. Strain broadening occurs due to the presence of defects in crystals. Such strain can be introduced via substitution of constituting atoms but also via special thermal treatment. It is possible to distinguish strain broadening from size broadening as the angle dependence is much larger than in the latter case.
4. Sample preparation height: Rotating sample holders improve the measurement statistics and thus provide the best results. However, they are not available for all machines. The most severe error during sample preparation is to fill the sample holder too high or too low. Both result in a significant shift of peak positions which can make the interpretation difficult.
Applications of XRD
Glass industry:
While glasses are X-ray amorphous and do not themselves give X-ray diffraction patterns, there are still manifold uses of XRD in the glass industry. They include identification of crystalline particles which cause tiny faults in bulk glass, and measurements of crystalline coatings for texture, crystallite size and crystallinity.
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