Kinetics of Intercalation in Lamellar Hosts Using Time-Resolved X-Ray Diffraction

1998 ◽  
pp. 153-158
Author(s):  
Dermot O’Hare ◽  
John S. O. Evans ◽  
Stephen Price
Keyword(s):  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Kinetics Of

Kinetics of Multi-Step Redox Processes by Time-Resolved In Situ X-ray Diffraction

2016 ◽  
Vol 88 (11) ◽  
pp. 1684-1692 ◽  
Author(s):  
Lukas C. Buelens ◽  
Vladimir V. Galvita ◽  
Hilde Poelman ◽  
Christophe Detavernier ◽  
Guy B. Marin
Keyword(s):  
Redox Processes ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Kinetics Of

Kinetics of the lamellar-inverse hexagonal phase transition determined by time-resolved x-ray diffraction

Biochemistry ◽  
1992 ◽  
Vol 31 (4) ◽  
pp. 1081-1092 ◽  
Author(s):  
Mark W. Tate ◽  
Erramilli Shyamsunder ◽  
Sol M. Gruner ◽  
Kevin L. D'Amico
Keyword(s):  
Phase Transition ◽  
Hexagonal Phase ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Kinetics Of

scholarly journals Spatiotemporal reaction kinetics of an ultrafast photoreaction pathway visualized by time-resolved liquid x-ray diffraction

2006 ◽  
Vol 103 (25) ◽  
pp. 9410-9415 ◽  
Author(s):  
T. K. Kim ◽  
M. Lorenc ◽  
J. H. Lee ◽  
M. Lo Russo ◽  
J. Kim ◽  
...  
Keyword(s):  
Reaction Kinetics ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Kinetics Of

Influence of oxygen partial pressure on the kinetics of YBa2Cu3O7−x formation

1994 ◽  
Vol 9 (2) ◽  
pp. 275-285 ◽  
Author(s):  
V. Milonopoulou ◽  
K.M. Forster ◽  
J.P. Formica ◽  
J. Kulik ◽  
J.T. Richardson ◽  
...  
Keyword(s):  
X Ray Diffraction ◽  
Decomposition Products ◽  
Time Resolved ◽  
X Ray ◽  
Formation Kinetics ◽  
Dimensional Diffusion ◽  
Diffusion Controlled ◽  
Gas Atmosphere ◽  
Kinetics Of

The YBa2Cu3O7−x formation kinetics from a spray-roasted precursor powder containing Y2O3, BaCO3, and CuO was followed via in situ, time-resolved x-ray diffraction as a function of gas atmosphere and temperature. In inert atmospheres, BaCO3 and CuO form BaCu2O2 which subsequently reacts with Y2O3 to form YBa2Cu3O6. However, YBa2Cu3O6 decomposes at temperatures exceeding 725 °C with Y2BaCuO5 being one of the decomposition products. In oxidizing atmospheres, YBa2Cu3O7−x formation involves the BaCuO2. At high temperatures (800–840 °C), oxygen increases the yield of YBa2Cu3O6. A nuclei growth model assuming two-dimensional, diffusion-controlled growth with second-order nucleation rate fits the experimental data.

Properties of Pure and Sulfided NiMoO4 and CoMoO4 Catalysts: Tpr, Xanes and Time-Resolved XRD Studdzs

1997 ◽  
Vol 497 ◽  
Author(s):  
S. Chaturvedi ◽  
J. A. Rodriguez ◽  
J. C. Hanson ◽  
A. Albornoz ◽  
J. L. Brito
Keyword(s):  
Electronic Properties ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
Direct Transformation ◽  
X Ray ◽  
Β Phase ◽  
Structural And Electronic Properties ◽  
X Ray Absorption ◽  
Kinetics Of ◽  
Cobalt And Nickel

ABSTRACTX-ray absorption near-edge spectroscopy (XANES) was used to characterize the structural and electronic properties of a series of cobalt- and nickel-molybdate catalysts (AMoO4.nH20, α-AMoO4, β-AMoO4; A= Co or Ni). The results of XANES indicate that the Co and Ni atoms are in octahedral sites in all these compounds, while the coordination of Mo varies from octahedral in the a-phases to tetrahedral in the β-phases and hydrate. Time-resolved x-ray diffraction shows a direct transformation of the hydrates into the β-AMoO4 compounds (following a kinetics of first order) at temperatures between 200 and 350 °C. This is facilitated by the similarities that the AMoO4.nH20 and β-AMoO4 compounds have in their structural and electronic properties. The molybdates react with H 2 at temperatures between 400 and 600 °C, forming gaseous water and oxides in which the oxidation state of Co and Ni remains +2 while that of Mo is reduced to +5 or +4. After exposing α-NiMoO4 and P-NiMoO4 to H2S, both metals get sulfided and a NiMoSx phase is formed. For the β phase of NiMoO4 the sulfidation of Mo is more extensive than for the a phase, making the former a better precursor for catalysts of hydrodesulfurization reactions.

In Situ Time-Resolved X-Ray Diffraction Investigation of the ω→ψ Transition in Al-Cu-Fe Quasicrystal-Forming Alloys

2007 ◽  
Vol 558-559 ◽  
pp. 943-947 ◽  
Author(s):  
E. Otterstein ◽  
R. Nicula ◽  
J. Bednarčík ◽  
M. Stir ◽  
E. Burkel
Keyword(s):  
Large Scale ◽  
Applied Pressure ◽  
High Temperature Phase ◽  
Temperature Phase ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
In Situ Xrd ◽  
Kinetics Of

Quasicrystals are aperiodic long-range ordered solids with a high potential for many modern applications. Interest is nowadays paid to the development of economically viable large-scale synthesis procedures of quasicrystalline materials involving solid-state transformations. The kinetics of the high-temperature phase transition from the complex ω-phase to the icosahedral quasicrystalline (iQC) ψ-phase in AlCuFe nanopowders was here examined by in-situ time-resolved X-ray diffraction experiments using synchrotron radiation. In-situ XRD experiments will allow insight on the influence of uniaxial applied pressure on the kinetics of phase transitions leading to the formation of single-phase QC nanopowders and further contribute to the optimization of sintering procedures for nano-quasicrystalline AlCuFe alloy powders.

Nucleation and growth kinetics of preferred C54 TiSi2 orientations: time-resolved x-ray diffraction measurements

2002 ◽  
Vol 92 (9) ◽  
pp. 5189-5195 ◽  
Author(s):  
A. S. Özcan ◽  
K. F. Ludwig ◽  
C. Lavoie ◽  
C. Cabral ◽  
J. M. E. Harper ◽  
...  
Keyword(s):  
Growth Kinetics ◽  
Nucleation And Growth ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Kinetics Of
Sign in / Sign up

Export Citation Format

Share Document