The detailed analysis of the obtained CMBs by means of FTIR,
XRD, and SEM is also performed.
These were duplicate samples from various studies; the selection criterion was that the quantity of the sample needed to be sufficient for
XRD analysis.
From the
XRD patterns, grain size for various phases was calculated, using Debye-Scherrer formula (Using K = 1).
2.2 FT-IR and
XRD Techniques comparison for Drug Classification
XRD was carried out to determine the quantitative crystallinity of the individual PPy:PSS composites synthesized through different pore sizes.
Finally, HPLC, UV-visible spectrophotometer and
XRD measurements were analysed.
X-ray diffraction (
XRD) is a ubiquitous technique to characterize crystal phases, as it produces a signal containing a series of peaks that serve as a fingerprint of the underlying atomic arrangement or crystal structure.
Within this scope, and in extension with earlier works, this study is aimed at quantifying using the
XRD modeling approach, the effect of an in situ applied hydrous perturbation on the hydration behavior and the structural changes of the most used host material in the earlier studies (i.e., the Na-exchanged montmorillonite).
XRD pattern can offer some structure information of materials, and Figure S1 in Supplementary Materials shows the
XRD pattern of 400 nm In film, where 400 nm In film shows no crystal
XRD peak, which means 400 nm In film presents noncrystal aggregation.
XRD. Figure 1(a) shows the
XRD pattern of Zn-HA with various zinc concentrations.
Additionally, Figure 2(b) depicts the insoluble part for inorganic materials that was measured by X-ray diffractometer and analyzed by the High Score Plus software to determine the phase identification of the X-ray powder diffraction (
XRD) data of the crystalline materials at the treated sludge samples.