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Diffraction pattern analysis

These are two important special cases. The power and simplicity of diffraction pattern analysis (crystallography) for the analysis of regular structure is a result of Eq. (2.27) and Eq. (2.25). No information is lost if infinite abstract lattices are subjected to Fourier transformation. [Pg.36]

D < 500 pm, Fraunhofer Diffraction Pattern Analysis (FDPA) can be employed in measuring particle size distributions (4,5). For the particles in the intermediate range, 0.7 pm < D < 10 pm, Mie theory of scattering holds and Turbidity Spectra (TS) can furnish information about particle sizes (6). [Pg.134]

WinPLOTR A Windows tool for powder diffraction pattern analysis, T. Roisnel and J. Rodriguez Carvajal, EPDIC 7 European Powder Diffraction, Pts 1 and 2 Materials Science Forum 378 3 118 123, Part 1 2 2001... [Pg.506]

FULLPROF. A Program for Rietveld Refinement and Pattern Matching Analysis, J. Rodriguez Carvajal, Abstracts of the Satellite Meeting on Powder Diffraction of the XV Congress of lUCr, (1990) Toulouse, France, p. 127 and WinPLOTR A Windows tool for powder diffraction pattern analysis, T. Roisnel and J. Rodriguez Carvajal, EPDIC 7 European Powder Diffraction, Pts 1 and 2 Materials Science Forum 378 3 118 123, Part 1 2 2001... [Pg.543]

Identification of polymorphism is ultimately based upon X-ray powder diffraction pattern analysis. Two forms of crystal must have two different diffraction patterns. Polymorphs... [Pg.30]

For SAPO-11 type materials it was observed (29) that the as synthesized SYN (with di-n propylamine template) the calcined (CAL), hydrated (WAT) and cyclohexane (CYC) saturated samples exhibit different XRD patterns as shown in fig.5. As for other molecular sieves it was important to determine if silicon was incorporated into the AIPO4 framework or not and subsequently if basic or acidic properties were induced depending if Si " was substituting Al or P ", respectively. The X-ray diffraction pattern analysis allowed us to show that A1 and P atoms are strictly alternate and that the material crystallizes in the non centro symmetric Ima2 space group with a = 1.867 (2), b= 1.3373 (2) and c = 0.84220 (9) nm (33). The channels along c axis are elliptical and are occupied by the di-n propylamine molecules. Disordered domains were also evidenced presumably... [Pg.30]

Diffraction pattern analysis from the MCM-41 idealised structure. [Pg.74]

Optical methods yield in principle results of high reproducibility if the withdrawal of a representative sample has been performed with care. The results obtained may however differ between instruments, due to systematical differences in the translation of the physical principle to the instrument by its manufacturer. The rapid determination of particle size distributions over at least two decades of particle size being the biggest advantage of optical methods. With diffraction pattern analysis, nowadays the time for the determination of a size distribution dropped to less than a minute. The results are plotted with respect to the diameter of a sphere. This diameter represents an equivalent diameter which is either calculated from the basic physical dependency or has been obtained from calibration. With optical methods one obtains the diameter of a sphere of equivalent light scattered, diffracted or extinguished. [Pg.409]

If one measures Apj at different tube lengths, T j, the relative amounts of particles, AQ3, of the corresponding settling rate classes, Wg, may in principle be calculated from the linear set of equations, described by Eqn. 17. The different velocity increases, Aej, for particles of a certain settling rate at position, T j, can be calculated from a force balance. Eqn. 17 represents a so-called first order Fredholm integral equation, well known from several optical methods, for example, diffraction pattern analysis. The problems encountered in the solution of this equation /12/ occur here as well. We suffered from this at the beginning of 1970, when we tried to set up an instrument according to P. Bernutat s idea.At that time we did not succeed for a number of reasons. To obtain a mathematical... [Pg.415]

T. Roisnel, J. Rodriguez-Carvajal, WinPLOTR a Windows tool for powder diffraction patterns analysis Materials Science Fomm, Proceedings of the Seventh European Powder Diffraction Conference (EPDIC 7), 118-123 (2000)... [Pg.246]

Leschonski, K., Rothele, S., Menzel, U., A Special Feeder for Diffraction Pattern Analysis of Dry Powders, Part. Charact, 1984, 1, 161-166. [Pg.177]

EDXA) and crystal structure by diffraction pattern analysis. TEM samples caii be taken on mixed cellulose ester membrane filters, but require special preparation. (See Baron, 1993.)... [Pg.179]

Stormer, H., Kleebe, H. J., Ziegler, G. (2007). Metastahle SiCN glass matrices studied by energy-filtered electron diffraction pattern analysis. Journal of Non-Crystalline Solids, 353(30-31), 2867-2877. doi 10.1016/j.jnoncrysol.2007.06.003. [Pg.243]


See other pages where Diffraction pattern analysis is mentioned: [Pg.173]    [Pg.40]    [Pg.463]    [Pg.208]    [Pg.133]    [Pg.137]    [Pg.139]    [Pg.300]    [Pg.4]    [Pg.525]    [Pg.360]    [Pg.130]    [Pg.316]    [Pg.262]    [Pg.177]    [Pg.247]    [Pg.611]    [Pg.76]    [Pg.409]    [Pg.11]    [Pg.109]   
See also in sourсe #XX -- [ Pg.134 , Pg.141 ]




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Diffraction analysis

Diffraction patterns

Electron diffraction pattern analysis

Fraunhofer diffraction pattern analysis

Pattern analysis

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