The study presented here was designed to provide information on the nature of fibres subjected to the action of raised temperature and on the possibility of determination of the incinerated material. X-ray powder diffraction was used as the most reliable method of identifying the composition of crys
On the Interpretation of X-Ray Diffraction Powder Patterns in Terms of the Nanostructure of Cellulose I Fibres
β Scribed by Christopher J. Garvey; Ian H. Parker; George P. Simon
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 174 KB
- Volume
- 206
- Category
- Article
- ISSN
- 1022-1352
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β¦ Synopsis
Abstract
Summary: The average lateral dimensions of cellulose microfibrils in paper sheets can be determined from the width of Xβray Bragg peaks at half the maximum height. The method assumes it is the finite size of the crystallite which is the main contributor to peak broadening in the directions orthogonal to the long axis of the crystallite. This assumption is examined in the context of samples from different botanical sources, of varying crystallinity and cellulose content and the various instrumental sources of broadening Xβray powder patterns. Excellent fits to the data from paper samples can be obtained by using five Voigt functions to the powder diffraction patterns, for the 101, $10\bar 1$, 021, 002 and 040 reflections. Of these reflections, the 020 is the clearest, and the best able to determine the lateral dimension of the crystallite. Results indicate that the size of microfibrils is dependent on the botanical source of the fibres.
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π SIMILAR VOLUMES
This study investigates the effects of crystal lattice deformation on the powder X-ray diffraction (PXRD) patterns of compressed polycrystalline specimen (compacts/tablets) made from molecular, crystalline powders. The displacement of molecules and the corresponding adjustment of interplanar distanc