scholarly journals X-ray powder diffraction in reflection geometry on multi-beam kJ-type laser facilities

2021 ◽  
Vol 92 (1) ◽  
pp. 013902
Author(s):  
A. Denoeud ◽  
J.-A. Hernandez ◽  
T. Vinci ◽  
A. Benuzzi-Mounaix ◽  
S. Brygoo ◽  
...  
Keyword(s):  
Powder Diffraction ◽  
X Ray ◽  
Reflection Geometry

A compact, transportable, thermoelectrically cooled cold stage for reflection geometry X-ray powder diffraction

2012 ◽  
Vol 45 (3) ◽  
pp. 608-610 ◽  
Author(s):  
Ian G. Wood ◽  
N. J. Hughes ◽  
F. Browning ◽  
A. D. Fortes
Keyword(s):  
Low Temperature ◽  
Powder Diffraction ◽  
Room Temperature ◽  
The Body ◽  
Base Temperature ◽  
Thermoelectric Cooling ◽  
X Ray ◽  
Temperature Range ◽  
Cold Stage ◽  
Reflection Geometry

A cold stage for Bragg–Brentano geometry X-ray powder diffraction is described for use in the temperature range from about 250 to 300 K. The stage is constructed in such a way that it may be removed from the diffractometer and pre-cooled to its base temperature before the sample is loaded. After loading, thermoelectric cooling maintains the specimen at low temperature (ice free) whilst the body of the stage is allowed to return to room temperature prior to remounting on the diffractometer.

New horizons for the structural characterization of stainless steel slags by X-ray powder diffraction

2007 ◽  
Vol 2007 (suppl_26) ◽  
pp. 61-66 ◽  
Author(s):  
B. Peplinski ◽  
B. Adamczyk ◽  
G. Kley ◽  
K. Adam ◽  
F. Emmerling ◽  
...  
Keyword(s):  
Stainless Steel ◽  
Powder Diffraction ◽  
Structural Characterization ◽  
X Ray ◽  
New Horizons

X-ray Structure Refinement and Vibrational Spectroscopy of Ca8Gd2 (PO4)6 O2

2013 ◽  
Vol 12 (10) ◽  
pp. 719-726
Author(s):  
R. Ayadi ◽  
Mohamed Boujelbene ◽  
T. Mhiri
Keyword(s):  
Solid State ◽  
General Formula ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
Solid State Reaction ◽  
Structure Refinement ◽  
Unit Cell ◽  
Cell Group ◽  
X Ray

The present paper is interested in the study of compounds from the apatite family with the general formula Ca10 (PO4)6A2. It particularly brings to light the exploitation of the distinctive stereochemistries of two Ca positions in apatite. In fact, Gd-Bearing oxyapatiteCa8 Gd2 (PO4)6O2 has been synthesized by solid state reaction and characterized by X-ray powder diffraction. The site occupancies of substituents is0.3333 in Gd and 0.3333 for Ca in the Ca(1) position and 0. 5 for Gd in the Ca (2) position.  Besides, the observed frequencies in the Raman and infrared spectra were explained and discussed on the basis of unit-cell group analyses.

Monitoring Polymer-Assisted Mechanochemical Cocrystallisation Through in Situ X-Ray Powder Diffraction

2020 ◽  
Author(s):  
Luzia S. Germann ◽  
Sebastian T. Emmerling ◽  
Manuel Wilke ◽  
Robert E. Dinnebier ◽  
Mariarosa Moneghini ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Powder Diffraction ◽  
Reaction Rate ◽  
Polymer Additives ◽  
Time Resolved ◽  
X Ray

Time-resolved mechanochemical cocrystallisation studies have so-far focused solely on neat and liquid-assisted grinding. Here, we report the monitoring of polymer-assisted grinding reactions using <i>in situ</i> X-ray powder diffraction, revealing that reaction rate is almost double compared to neat grinding and independent of the molecular weight and amount of used polymer additives.<br>

Crystal Transition and Drug-excipient Compatibility of Clarithromycin in Sustained Release Tablets

2020 ◽  
Vol 16 (7) ◽  
pp. 950-959
Author(s):  
Yu Li ◽  
Xiangwen Kong ◽  
Fan Hu
Keyword(s):  
Sustained Release ◽  
Powder Diffraction ◽  
Magnesium Stearate ◽  
Influential Factor ◽  
High Concentration ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Sustained Release Tablets ◽  
Crystal Transition ◽  
Excipient Compatibility

Background: Clarithromycin is widely used for infections of helicobacter pylori. Clarithromycin belongs to polymorphic drug. Crystalline state changes of clarithromycin in sustained release tablets were found. Objective: The aim of this study was to find the influential factor of the crystal transition of clarithromycin in preparation process of sustained-release tablets and to investigate the possible interactions between the clarithromycin and pharmaceutical excipients. Methods and Results: The crystal transition of active pharmaceuticals ingredients from form II to form I in portion in clarithromycin sustained release tablets were confirmed by x-ray powder diffraction. The techniques including differential scanning calorimetry and infrared spectroscopy, x-ray powder diffraction were used for assessing the compatibility between clarithromycin and several excipients as magnesium stearate, lactose, sodium carboxymethyl cellulose, polyvinyl-pyrrolidone K-30 and microcrystalline cellulose. All of these methods showed compatibilities between clarithromycin and the selected excipients. Alcohol prescription simulation was also done, which showed incompatibility between clarithromycin and concentration alcohol. Conclusion: It was confirmed that the reason for the incompatibility of clarithromycin with high concentration of alcohol was crystal transition.

X-RAY POWDER DIFFRACTION ANALYSIS OF SOIL SAMPLES FROM THE NAVESINK FORMATION IN MONMOUTH COUNTY, NEW JERSEY

2020 ◽  
Author(s):  
Miranda Maliszka ◽  
◽  
Sabrina Sobel ◽  
Anthony Johnson ◽  
Dennis Radcliffe
Keyword(s):  
New Jersey ◽  
Diffraction Analysis ◽  
Powder Diffraction ◽  
Soil Samples ◽  
X Ray ◽  
Monmouth County
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