Dynamic steady state during cyclic diffusional phase transformations

2002 ◽  
Vol 91 (11) ◽  
pp. 9083-9090 ◽  
Author(s):  
Christopher A. Schuh
2019 ◽  
Vol 25 (4) ◽  
pp. 230 ◽  
Author(s):  
Boris Straumal ◽  
Askar Kilmametov ◽  
Andrey Mazilkin ◽  
Olga Kogtenkova ◽  
Brigitte Baretzky ◽  
...  

<p class="AMSmaintext"><span lang="EN-GB">Severe plastic deformation (SPD) can induce various phase transformations. After a certain strain, the dynamic equilibrium establishes between defects production by an external force and their relaxation (annihilation). The grain size, hardness, phase composition etc. in this steady-state does not depend on the initial state of a material and is, therefore, equifinal. In this review we discuss the competition between precipitation and dissolution of precipitates, amorphization and (nano)crystallization, SPD-induced accelerated mass-transfer, allotropic and martensitic transitions and formation of grain boundary phases.</span></p>


An analysis of the growth characteristics of a train of ledges is presented, where volume diffusion in the parent phase is assumed to be the rate­- controlling factor. First a train of steps of unequal height is considered where the step heights are assumed to be consistent with a steady-state motion so that each step moves with the same speed. It is possible to analyse this situation by asymptotic methods when the steps are either far apart or close together. Explicit results are given for both two- and three-step trains and it is shown how the step heights must vary if a given train is to move steadily at a specified speed. Trains of steps of equal height are also considered and an analysis is made of the relative velocities of such steps due to their interaction.


2006 ◽  
Vol 918 ◽  
Author(s):  
Guy J. Adriaenssens

AbstractAnnealing at 150 °C induces phase separation in amorphous (Ge2Se7)88Bi5Sb7 bulk samples. Spectrally resolved steady-state photoconductivity measurements indicate the presence of crystalline Bi2Se3 clusters in the annealed material, but also the subsequent gradual disappearance of this microstructure at room temperature. Similar annealing-induced metastable changes are observed in other elements of a (Ge2Se7)88BixSb12-x sample series.


2011 ◽  
Vol 83 (5) ◽  
pp. 1105-1112
Author(s):  
Ernst Gamsjäger

It is a prerequisite for the occurrence of diffusive phase transformations that the system is in an off-equilibrium condition. The time-dependent development of the variables until equilibrium or steady-state conditions are reached can be calculated by solving the evolution equations that can be derived from the principle of maximum entropy production. These equations provide the theoretical framework for the kinetics of diffusive phase transformations. In this work, the development from sharp interface-local equilibrium (SI-LE) models to thick interface-finite mobility (TI-FM) models is reviewed and presented in the light of the above-mentioned principle. Experimental results indicate that the kinetics of diffusive solid-state phase transformations can, at least in certain ranges of composition and temperature, be modeled in a satisfactory manner by the TI-FM approach only.


Author(s):  
R. C. Moretz ◽  
G. G. Hausner ◽  
D. F. Parsons

Use of the electron microscope to examine wet objects is possible due to the small mass thickness of the equilibrium pressure of water vapor at room temperature. Previous attempts to examine hydrated biological objects and water itself used a chamber consisting of two small apertures sealed by two thin films. Extensive work in our laboratory showed that such films have an 80% failure rate when wet. Using the principle of differential pumping of the microscope column, we can use open apertures in place of thin film windows.Fig. 1 shows the modified Siemens la specimen chamber with the connections to the water supply and the auxiliary pumping station. A mechanical pump is connected to the vapor supply via a 100μ aperture to maintain steady-state conditions.


Author(s):  
P. G. Kotula ◽  
D. D. Erickson ◽  
C. B. Carter

High-resolution field-emission-gun scanning electron microscopy (FESEM) has recently emerged as an extremely powerful method for characterizing the micro- or nanostructure of materials. The development of high efficiency backscattered-electron detectors has increased the resolution attainable with backscattered-electrons to almost that attainable with secondary-electrons. This increased resolution allows backscattered-electron imaging to be utilized to study materials once possible only by TEM. In addition to providing quantitative information, such as critical dimensions, SEM is more statistically representative. That is, the amount of material that can be sampled with SEM for a given measurement is many orders of magnitude greater than that with TEM.In the present work, a Hitachi S-900 FESEM (operating at 5kV) equipped with a high-resolution backscattered electron detector, has been used to study the α-Fe2O3 enhanced or seeded solid-state phase transformations of sol-gel alumina and solid-state reactions in the NiO/α-Al2O3 system. In both cases, a thin-film cross-section approach has been developed to facilitate the investigation. Specifically, the FESEM allows transformed- or reaction-layer thicknesses along interfaces that are millimeters in length to be measured with a resolution of better than 10nm.


Author(s):  
K. Barmak

Generally, processing of thin films involves several annealing steps in addition to the deposition step. During the annealing steps, diffusion, transformations and reactions take place. In this paper, examples of the use of TEM and AEM for ex situ and in situ studies of reactions and phase transformations in thin films will be presented.The ex situ studies were carried out on Nb/Al multilayer thin films annealed to different stages of reaction. Figure 1 shows a multilayer with dNb = 383 and dAl = 117 nm annealed at 750°C for 4 hours. As can be seen in the micrograph, there are four phases, Nb/Nb3-xAl/Nb2-xAl/NbAl3, present in the film at this stage of the reaction. The composition of each of the four regions marked 1-4 was obtained by EDX analysis. The absolute concentration in each region could not be determined due to the lack of thickness and geometry parameters that were required to make the necessary absorption and fluorescence corrections.


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