Time Resolved X-Ray Diffraction Study of the Transformation Kinetics of TiSi2-C49 in Amorphous Si/Ti Multilayers

1993 ◽  
Vol 311 ◽  
Author(s):  
J. Sariel ◽  
Haydn Chen ◽  
J. F. Jongste ◽  
S. Radelaar

ABSTRACTAmorphous Si/Ti multilayers transform at high temperatures (above 700°C) to TiSi2-C54. This phase is important for microelectronics applications because of its low resistivity, stability up to 900°C, and compatibility with silicon processing. However, an unfavorable metastable TiSi2-C49 phase is usually formed at lower temperatures. Thus, an understanding of the C49 phase formation kinetics is useful to the device processing strategy. The kinetics of the transformation of TiSi2-C49 phase can be characterized as a process of nucleation and growth, using the well known Johnson Mehl Avrami (JMA) equation. In the present work the formation kinetics of the C49 phase has been studied by an in situ x-ray diffraction technique. Isothermal annealing in vacuum was done at four temperatures, in the range of 275"C to 310°C. A position sensitive detector (PSD) was used to simultaneously collect the diffracted beams of (131) and (150) peaks of the C49 phase. From the data, the Avrami exponent, n, was determined to be 2.0±0.1. The reaction rate constant k follows a familiar Arrhenius-type equation with a measured activation energy of 2.5eV. Comparison of our x-ray results with kinetic data obtained by other means will be discussed.

2011 ◽  
Vol 306-307 ◽  
pp. 966-969
Author(s):  
Chun Fang Wang ◽  
Zong Hui Zhou ◽  
Cai Xia Liu ◽  
Xin Cheng

Through testing the amount of the free lime and the Loss ignition, the clinker formation rate, the reaction-rate constant (K) and the activation energy (Ea) were calculated according to the Gentling equation and Arrhenius equation. The effects of CaF2on the formation kinetics of Portland cement clinker were investigated by analyzing theKandEa. X-ray diffraction (XRD) and scanning electron Microscope (SEM) were used to characterize the phase composition and the morphology of the resulting samples. The results show that the silicate minerals formation is promoted when a proper amount of CaF2is doped into the raw meal. TheKincreased from 0.7450 ×10-5s-1to 7.1588 ×10-5s-1and theEadecreased from 386 kJ/mol to 122 kJ/mol when the amount of CaF2increased from 0.0% to 2.0% in mass. However, the results were reversed at the amount of CaF2exceeding 2%.


1994 ◽  
Vol 9 (2) ◽  
pp. 275-285 ◽  
Author(s):  
V. Milonopoulou ◽  
K.M. Forster ◽  
J.P. Formica ◽  
J. Kulik ◽  
J.T. Richardson ◽  
...  

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.


Author(s):  
Dermot O’Hare ◽  
John S. O. Evans ◽  
Stephen Price

2016 ◽  
Vol 88 (11) ◽  
pp. 1684-1692 ◽  
Author(s):  
Lukas C. Buelens ◽  
Vladimir V. Galvita ◽  
Hilde Poelman ◽  
Christophe Detavernier ◽  
Guy B. Marin

Biochemistry ◽  
1992 ◽  
Vol 31 (4) ◽  
pp. 1081-1092 ◽  
Author(s):  
Mark W. Tate ◽  
Erramilli Shyamsunder ◽  
Sol M. Gruner ◽  
Kevin L. D'Amico

1995 ◽  
Vol 398 ◽  
Author(s):  
A. Tomasi ◽  
E. Galvanetto ◽  
F.C. Matacotta ◽  
P. Nozar ◽  
P. Scardi ◽  
...  

ABSTRACTA systematic study on phase formation and stabilisation in the Ba-Cu-C-O system in the temperature range 20-500°C, under various atmospheres, by traditional thermal analysis techniques, high temperature X-ray diffraction and high resolution electron microscopy, has permitted to identify and characterise the formation kinetics of a new copper containing phase isomorphic to γ-BaCO3.


2006 ◽  
Vol 103 (25) ◽  
pp. 9410-9415 ◽  
Author(s):  
T. K. Kim ◽  
M. Lorenc ◽  
J. H. Lee ◽  
M. Lo Russo ◽  
J. Kim ◽  
...  

1997 ◽  
Vol 497 ◽  
Author(s):  
S. Chaturvedi ◽  
J. A. Rodriguez ◽  
J. C. Hanson ◽  
A. Albornoz ◽  
J. L. Brito

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.


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