Search results for "Powder diffraction"
showing 10 items of 243 documents
High pressure in-situ X-ray diffraction study on Zn-doped magnetite nanoparticles
2018
We have performed high pressure synchrotron X-ray powder diffraction experiments on two different samples of Zn-doped magnetite nanoparticles (formula Fe(3-x)ZnxO4; x = 0.2, 0.5). The structural behavior of then a noparticles was studied up to 13.5 GPa for x = 0.2, and up to 17.4 GPa for x = 0.5. We have found that both systems remain in the cubic spinel structure as expected for this range of applied pressures. The analysis of the unit cell volume vs. pressure results in bulk modulus values lower than in both end-members, magnetite (Fe3O4) and zinc ferrite (ZnFe2O4), suggesting that chemical disorder may favor compressibility, which is expected to improve the increase of the Neel temperatu…
Rapid nanocrystallization of soft-magnetic amorphous alloys using microwave induction heating
2009
The crystallization of Fe73Nb3Cu1Si16B7 alloy during microwave heating was investigated in situ using synchrotron radiation powder diffraction. The phase transformation comprises a primary nanocrystallization stage and a final microcrystallization step. We provide evidence for a strong enhancement of the transformation kinetics. Microwave heating occurs as a result of both ohmic and magnetic losses induced by eddy currents, which defines a volumetric microwave induction heating process. Nanocrystallization is completed within 5 s, while full crystallization is achieved in less than 10 s.
Synthesis and Characterization of SiC/MC/C Ceramics (M = Ti, Zr, Hf) Starting from Totally Non-oxidic Precursors
2002
The reaction of poly(dimethylsilane) (PDMS) and poly(dimethylcarbosilane) (PCS) with bis(cyclopentadienyl)M dichloride Cp2MCl2 (M ) Ti, Zr, Hf) complexes has been used as a new route to obtain ceramic materials based on SiC-containing M. The reaction is completed at a relatively low temperature, 900 °C, yielding the corresponding amorphous SiC/MC ceramics which have been characterized by means of 29 Si MAS NMR. These amorphous materials have been treated at higher temperatures, 1350 °C, under a purified argon atmosphere, yielding partially crystallized products which have been studied by X-ray powder diffraction and 29 Si MAS NMR. The effect of the composition of the mixture of precursors is
Permanent magnetism in apoferritin-encapsulated Pd nanoparticles
2007
Pd nanoparticles have been prepared within the apoferritin cavity. X-Ray powder diffraction, transmission electronic microscopy and magnetization measurements have been used for characterizing the nanoparticles. The nanoparticles exhibit permanent magnetism at room temperature.
Structural and magnetic characterization of Pd nanoparticles encapsulated in apoferritin
2010
Pd nanoparticles exhibiting permanent magnetism at room temperature have been prepared within the apoferritin cavity. Pd nanoparticles in air and under an inert atmosphere were synthesized to study the influence of the aerobic and anaerobic conditions in the final magnetic properties. The surface of nanoparticles as well as the type of crystalline phase could determine the magnetic properties. X-ray powder diffraction, including Debye-function analysis, transmission electronic microscopy, and magnetization measurements have been used for characterizing the nanoparticles.
Quantitative X-Ray Powder Diffraction Analysis of Some Feldspars Used as Raw Material in Ceramics
2001
Crystal structures of new ternary compounds in RE–Pt–Pb and RE–Au–Pb systems (RE=rare earth metal)
2012
Abstract The crystal structures of the compounds RE 2 Pt 2 Pb (RE = Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu; Mo 2 FeB 2 structure type, space group P 4/ mbm , Pearson code tP10 ), REPtPb (RE = La, Ce, Pr, Nd, Sm; ZrNiAl structure type, space group P 6 ¯ 2 m , Pearson code hP9 ), RE 2 Au 2 Pb (RE = Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu; Er 2 Au 2 Sn structure type, space group P 4 2 / mnm , Pearson code tP20 ) and REAuPb (RE = Tm, Yb and Lu) were determined using X-ray powder diffraction.
Desummation of Mixed Powder Diffraction Lines
1991
Determination of Molecular Crystal Structures from X-Ray Powder Diffraction Data
1993
“Ab-initio” structure solution of nano-crystalline minerals and synthetic materials by automated electron tomography
2012
Most of the newly discovered mineral phases, as well as many new synthesized industrial materials, appear only in the form of nano crystals, with a size not sufficient for single-crystal x-ray structure analysis. The development of techniques able to investigate the structure of nano crystalline materials is therefore one of the most important frontiers of crystallography. The most widespread technique providing relatively fast and well consolidated routes for structure analysis of bulk materials is x-ray powder diffraction (XRPD). Nevertheless, XRPD suffers from intrinsic 1-dimension reduction of information that greatly limits its applicability in presence of peak broadening and overlappi…