Oxygen Diffusivity of La0.6Sr0.4Co0.2Fe0.8O3-δ Perovskite Oxide

2012 ◽  
Vol 616-618 ◽  
pp. 633-637
Author(s):  
Yan Wei Liu ◽  
Zhe Lü

La0.6Sr0.4Co0.2Fe0.8O3-δ composite oxide was prepared and characterized. Dilatometer and four-probe DC were exploited to investigate the thermal expansion and electrical conductivity, respectively. The thermal expansion curve was linear, but it became steeper at the high temperature region, as a result of the loss of lattice oxygen and the formation of oxygen vacancies. The conductivity increased with temperature up to about 600oC, and then decreased due to the loss of lattice oxygen. The maximum conductivity was more than 300 S cm-1. The chemical diffusion coefficient in La0.6Sr0.4Co0.2Fe0.8O3-δ was estimated by analyzing the conductivity relaxation behavior. The relaxation process of the conductivity change for La0.6Sr0.4Co0.2Fe0.8O3-δ was traced as a function of time, at a fixed temperature. It was found that the chemical diffusion coefficients measured at temperatures 720-770oC vary from 710-8 to 110-7 cm2 S-1. The activation energy for oxygen diffusion in La0.6Sr0.4Co0.2Fe0.8O3-δ, derived from the chemical diffusion coefficient is 40.8±3.6 kJ mol-1.

2020 ◽  
Vol 18 (1) ◽  
pp. 1895-1914
Author(s):  
Linlin Meng ◽  
Wen-Qing Xu ◽  
Shu Wang

Abstract We study the boundary layer problem of a Keller-Segel model in a domain of two space dimensions with vanishing chemical diffusion coefficient. By using the method of matched asymptotic expansions of singular perturbation theory, we construct an accurate approximate solution which incorporates the effects of boundary layers and then use the classical energy estimates to prove the structural stability of the approximate solution as the chemical diffusion coefficient tends to zero.


1972 ◽  
Vol 27 (7) ◽  
pp. 1109-1118 ◽  
Author(s):  
Chr. Herzig ◽  
Th. Heumann

Abstract The diffusion of Sn-113 and Au-195 in pure gold and dilute tin -gold alloys has been measured at different temperatures and tin concentrations in coarse-grained specimens. In addition the dependence on concentration of the chemical diffusion coefficient and the diffusion of tin in gold at very low impurity concentrations has been determined using the electron microprobe. It was found, that the self-diffusion coefficient of tin as well as that of gold increased strongly with in-creasing impurity content. The thermodynamic factor is equal to one up to ca. 0.5 at.-% tin. For the correlation factor of the diffusion of tin in gold, calculated by the relation of Lidiard, an essentially temperature independent value is obtained. A comparison of the experimental results with the model of Le Claire concerning the impurity diffusion in metals shows, that this model seems to require a too-large temperature dependence of the correlation factor


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