Diffractogram

The breadth of the peaks in an x-ray diffractogram provide a detennination of the average crystallite domain size, assuming no lattice strain or defects, tlirough the Debye-Scherr fonnula ... 

A 1.0 nm basal spacing exhibited in a diffractogram peak that is somewhat broad and diffuse and skewed toward wider spacings characterizes the x-ray diffraction pattern of iUite. Polymorphs may be present (120). Muscovite derivatives are typicaUy dioctahedral phlogopite derivatives are trioctabedral. 

Conversion to cellulose II and cellulose III via caustic mercerization and Hquid ammonia treatment are commercial textile processes that are discussed later. Figure 7 shows the characteristic diffractograms (CuKa radiation) of native cellulose, cellulose mercerized with sodium hydroxide, and cellulose treated with Hquid ammonia. 

Figure 2 X-ray diffractograms of P7MB obtained at different temperatures [10]. Curve a 182°C curve b 152°C curve c ITC. Noise has been suppressed.

Figure 9 Ambient-temperature x-ray diffractograms of PDTMB samples (a) annealed at 70°C for 24 days, and (b) freshly quenched from the melt [25,26]. Noise has been suppressed.

The x-ray diffractograms of those three samples are shown in Fig. 12. The lower pattern corresponds to the quenched sample where only the mesophase is present (the layer line, appearing at lower angles is not shown). The other two diagrams corresponding to the annealed samples present several sharp diffraction peaks, which... 

Figure 2. XRD pattern of an EMD sample (Chemetals). The diffractogram is taken with a Bruker AXS D5005 diffractometer using CuKa radiation and a scintillation counter. The step width is 0.02° with a constant counting time of 10 s / step.

Fig. 4. X-ray diffractograms of DECA (1), HIPS/DECA-l-Sb203 (2), and manually ground DECA (3)... 

FIGURE 2.9 X-ray diffractogram (XRD) spectra of unmodified and modified nanoclays and styrene-butadiene rubber (SBR)-based nanocomposites with styrene content of (a) 15% and 40% and (b) 23%. (From Sadhu, S. and Bhowmick, A.K., J. Polym. Set, Part B Polym. Phys., 42, 1573, 2(304. Courtesy of Wiley InterScience.)... 

Figure 4.4. X-rays scattered by atoms in an ordered lattice interfere constructively in directions given by Bragg s law. The angles of maximum intensity enable one to calculate the spacings between the lattice planes and allow furthermore for phase identification. Diffractograms are measured as a function of the angle 26. When the sample is a...

The analysis of XRPD patterns is an important tool studying the crystallographic structure and composition of powder compounds including the possibility to study deviation from ideal crystallinity, i.e. defects. Looking at an X-ray powder diffractogram the peak position reflects the crystallographic symmetry (unit cell size and shape) while the peak intensity is related to the unit cell composition (atomic positions). The shape of diffraction lines is related to defects , i.e. deviation from the ideal crystallinity finite crystallite size and strain lead to broadening of the XRPD lines so that the analysis of diffraction line shape may supply information about sample microstructure and defects distribution at the atomic level. 

Figure 1 X-ray powder diffractograms of the crystalline and amorphous forms of nedocromil sodium trihydrate. I is the intensity of the diffracted beam at a diffraction angle 9. (RK Khankari and DJW Grant, unpublished observations.)...

Figure 2 X-ray diffractograms recorded at room temperature, (a) Metallocene-synthesized isotactic poly(propylene), mmmm — 0.996 crystallized at 145°C. (b) Atactic poly(propylene). Reproduced with permission from Ref. [43], Copyright John Wiley Sons, Inc., 1999.

When the diffractogram of the pure amorphous polymer is not available at room temperature, the shape of the halo can be deduced either by peak fitting or estimating the halo pattern from the corresponding shape of the molten material. The uncertainties associated with these methodologies arise from the need to give a... 

Figure 4.1. Removal of carbonate from Israeli arid soils as indicated by the X-ray diffractograms after extraction of the carbonate fraction by NaOAc-HOAc solutions at various pHs for 16 hours. C calcite d = 3.04 A, and D dolomite, d = 2.89 A. Number 1, 2, 3, 4, 5, and 6 indicate non-treated soil (No. 1), treatments (No. 2-6) with NaOAc-HOAc solutions at pH 7.0, 6.0, 5.5, 5.0 and 4.0, respectively (after Han and Banin, 1995. Reprinted from Commun Soil Sci Plant Anal, 26, Han and Banin A., Selective sequential dissolution techniques for trace metals in arid-zone soils The carbonate dissolution step, p 563, Copyright (1995), with permission from Taylor Francis US)...

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