The Study of Surface Self-Diffusion Mass Transport by Measurements of the Morphological Evolution of Tips

Author(s):  
M. Drechsler
Author(s):  
Bartek Wierzba ◽  
Jolanta Romanowska ◽  
Maryana Zagula-Yavorska ◽  
Janusz Markowski ◽  
Jan Sieniawski

AbstractThe generalized Darken method allows a quantitative description of diffusion mass transport in multi-phase materials. The method characterizes the diffusion zone by phase volume fractions. The results of the calculations are compared with experimental concentration’s profiles of nickel, zirconium and aluminum in zirconium doped aluminide coatings deposited on pure nickel by the PVD and CVD methods.


Author(s):  
Lalit M. Pant ◽  
Sushanta K. Mitra ◽  
Marc Secanell

Porous transport layers are an integral part of polymer electrolyte fuel cells (PEMFC). In order to optimize the catalyst layer performance and reduce catalyst consumption, a thorough understanding of mass transport through porous media is necessary. Currently, there is a lack of experimental measurements of effective mass transport properties of porous transport layers. Further, mass transport theories in the literature, such as the binary friction model by Kerkhof [1], have not been extensively validated for porous media. In the present study, mass transport measurements have been performed on the porous media of a PEMFC, namely a GDL and an MPL. The experimental setup described by Pant et al. [2] has been used. The setup uses the diffusion bridge/counter-diffusion technique for the mass transport measurements. The experimental setup has the advantage that it can be used to perform studies for pure diffusion and convection-diffusion mass transport. The setup also facilitates measurement of permeability of porous media, which can then be used in convection-diffusion studies. Preliminary permeability measurements of GDL and MPL from the setup show good agreement with values available in literature. In preliminary experimentation, the conventional diffusivity correlations like Bruggeman equation have been found to overpredict the diffusivities.


1995 ◽  
Vol 399 ◽  
Author(s):  
H. Brune ◽  
K. Bromann ◽  
K. Kern

ABSTRACTA general concept is shown how to measure both the barriers for terrace and step-down diffusion for an epitaxial system. It is based on the application of mean-field nucleation theory to variable temperature STM data. With this approach we studied the influence of strain on intra- and interlayer diffusion for Ag self diffusion on strained and unstrained Ag(111) surfaces. The strained surface was the first Ag layer that grows pseudomorphically on Pt(111) and is thus under 4.2% compressive strain. The barrier for terrace diffusion is observed to be substantially lower on the strained, compared to the unstrained Ag/Ag(111) case, 60±10 meV and 97±10 meV, respectively. The additional barrier for interlayer diffusion decreases from 120±15 meV for Ag(111) homoepitaxy to only 30±5 meV for diffusion from the strained Ag layer down to the Pt(111) substrate. These examples illustrate the considerable effect of strain on the intra- and interlayer mass transport. They require a new concept of layer dependent nucleation kinetics for heteroepitaxial systems in general.


2006 ◽  
Vol 251-252 ◽  
pp. 123-126 ◽  
Author(s):  
Yuriy S. Nechaev

Urgent open questions and their solution ways are considered of the thermodynamic stimuli and mechanisms of the enhanced Fickian diffusion mass-transport providing the unusual structuralphase transformations in metallic materials undergoing the intensive cold deformation, those can not be described in the framework of the conventional phase diagrams.


RSC Advances ◽  
2016 ◽  
Vol 6 (102) ◽  
pp. 99704-99713 ◽  
Author(s):  
Hari Krishna Chilukoti ◽  
Gota Kikugawa ◽  
Taku Ohara

The asymmetric self-diffusion characteristics of binary n-alkane mixtures in the first adsorption layer near α-quartz substrate were demonstrated and discussed.


2002 ◽  
Vol 752 ◽  
Author(s):  
Nieck E. Benes ◽  
Henk Verweij

ABSTRACTMaterials research involves many areas for which a proper understanding of multi-component mass transport is essential. Examples include sintering and transport-limited reaction in syntheses. In addition, materials may be principally designed for direct manipulation of mass transport, as in membrane materials. Macroscopic descriptions for mass transport are available, but physical interpretation of related transport parameters is generally not straightforward and often relies on microscopic considerations. We will show that, even for diffusion in a simple ideal Langmuir type lattice, macroscopic theories should be used with caution. Differences in mobilities of dissimilar species can set off percolation behavior, causing the flux of the more mobile species to vanish. Such behavior is, for instance, observed for zeolite membranes and cannot be predicted by commonly accepted macroscopic transport theories. Correlations between successive movements of molecules cause a decrease in the self-diffusion coefficient, DS. For non-equilibrium transport it can be shown that correlation effects in most cases disappear in which case non-equilibrium transport becomes related to the component diffusion coefficient D, instead of the smaller DS.


2016 ◽  
Vol 9 ◽  
pp. 58-72 ◽  
Author(s):  
U. Sarder ◽  
Alexander V. Evteev ◽  
Elena V. Levchenko ◽  
A. Kromik ◽  
I.V. Belova ◽  
...  

In this study, mass transport properties of liquid Cu-Ag alloys are investigated over wide temperature and composition ranges. The calculations are performed within the framework of the Green-Kubo (GK) formalism by using equilibrium molecular dynamics (MD) simulations along with one of the most reliable embedded-atom method potentials for this system developed by [P. Williams et al.: Modell. Simul. Mater. Sci. Eng. vol. 14 (2006), p. 817]. The approach employed allows for evaluation of the components’ self-diffusion coefficients as well as the phenomenological coefficient for mass transport Lcc. The results obtained in this study can be used to predict the kinetics of solidification of real liquid Cu-Ag alloys.


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