Anionic and Cationic Diffusion in Ionic Conducting Oxides

2005 ◽  
Vol 237-240 ◽  
pp. 843-848 ◽  
Author(s):  
Georgette Petot-Ervas ◽  
C. Petot ◽  
Jean Marc Raulot ◽  
J. Kusinski

This paper concerns an analysis of the transport processes at high temperature in anionic conducting oxides subjected to a chemical potential gradient or an applied electrical field. The general equations are given. The principle of the cationic kinetic demixing under a “generalized“ thermodynamical potential gradient is reviewed. Experimental results obtained with yttria-doped zirconia are reported. An experimental procedure for the determination of the oxygen diffusion coefficient in ionic and semiconducting oxides is also described. The results obtained with yttriastabilized zirconia are compared to both self diffusion and conductivity data. This has allowed us to obtain information concerning the defect structure.

2004 ◽  
Vol 71 (5) ◽  
pp. 646-651 ◽  
Author(s):  
Z. Suo

In a single-component material, a chemical potential gradient or a wind force drives self-diffusion. If the self-diffusion flux has a divergence, the material deforms. We formulate a continuum theory to be consistent with this kinematic constraint. When the diffusion flux is divergence-free, the theory decouples into Stokes’s theory for creep and Herring’s theory for self-diffusion. A length emerges from the coupled theory to characterize the relative rate of self-diffusion and creep. For a flow in a film driven by a stress gradient, creep dominates in thick films, and self-diffusion dominates in thin films. Depending on the film thickness, either stress-driven creep or stress-driven diffusion prevails to counterbalance electromigration. The transition occurs when the film thickness is comparable to the characteristic length of the material.


1983 ◽  
Vol 80 ◽  
pp. 315-323 ◽  
Author(s):  
Marc Lindheimer ◽  
Jean-Claude Montet ◽  
Roselyne Bontemps ◽  
Jacques Rouviere ◽  
Bernard Brun

Author(s):  
Tobias Förster ◽  
Artur Blivernitz

AbstractThis work describes a newly introduced experimental procedure to quantify the diffusion progress of mineral oils locally resolved in NBR. Diffusion of reference oils IRM 901, IRM 902 and IRM 903 in NBR with various acrylonitrile contents was investigated. Classical sorption experiments were performed as a basic characterization and compared to the newly introduced method. Here, elastomer specimens are only being dipped with the bottom in a relatively small reservoir of mineral oil. This provides a determination of locally resolved concentration profiles of mineral oils, and the calculation of diffusion coefficients. These diffusion coefficients follow the same trends like those determined via sorption experiments. Despite differences in the absolute numbers, activation energies of diffusion can be applied as a suitable measure for the compatibility of elastomers and fluids.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1288
Author(s):  
Thi Thuy Nguyen ◽  
Fayna Mammeri ◽  
Souad Ammar ◽  
Thi Bich Ngoc Nguyen ◽  
Trong Nghia Nguyen ◽  
...  

The formation of silver nanopetal-Fe3O4 poly-nanocrystals assemblies and the use of the resulting hetero-nanostructures as active substrates for Surface Enhanced Raman Spectroscopy (SERS) application are here reported. In practice, about 180 nm sized polyol-made Fe3O4 spheres, constituted by 10 nm sized crystals, were functionalized by (3-aminopropyl)triethoxysilane (APTES) to become positively charged, which can then electrostatically interact with negatively charged silver seeds. Silver petals were formed by seed-mediated growth in presence of Ag+ cations and self-assembly, using L-ascorbic acid (L-AA) and polyvinyl pyrrolidone (PVP) as mid-reducing and stabilizing agents, respectively. The resulting plasmonic structure provides a rough surface with plenty of hot spots able to locally enhance significantly any applied electrical field. Additionally, they exhibited a high enough saturation magnetization with Ms = 9.7 emu g−1 to be reversibly collected by an external magnetic field, which shortened the detection time. The plasmonic property makes the engineered Fe3O4-Ag architectures particularly valuable for magnetically assisted ultra-sensitive SERS sensing. This was unambiguously established through the successful detection, in water, of traces, (down to 10−10 M) of Rhodamine 6G (R6G), at room temperature.


1989 ◽  
Vol 39 (8) ◽  
pp. 5025-5034 ◽  
Author(s):  
G. Vogl ◽  
W. Petry ◽  
Th. Flottmann ◽  
A. Heiming

1997 ◽  
Vol 272 (2) ◽  
pp. R640-R647 ◽  
Author(s):  
O. A. Candia ◽  
T. Yorio

The amphibian skin represents an important organ for osmoregulation and, like the mammalian kidney, maintains acid-base balance by secreting protons or base. However, the lack of a reliable and accurate method to measure the contribution of unidirectional fluxes of HCO3- ions to this mechanism has been an obstacle for the determination of the role of bicarbonate in epithelial acid-base homeostasis. Recently, one of us developed a method that allows for the reliable determination of transepithelial fluxes of bicarbonate, and this method was applied to determine unidirectional fluxes of (14)CO2 and H(14)CO3 under a variety of conditions. We report that the combined CO2 and HCO3- mucosal-to-serosal flux under 5% CO2 was 40% larger than the opposing flux, giving a net flux in the mucosal-to-serosal direction. This net flux was inhibited by acetazolamide. In CO2-free conditions, there was no detectable net flux; however, acetazolamide and PGF(2alpha) attenuated the mucosal-to-serosal flux and established an apparent secretion of HCO3-. A model is presented that depicts twelve vectors or components to the CO2 plus HCO3- fluxes in the frog skin. This model can accurately reproduce the experimental values measured from unidirectional fluxes of CO2 and HCO3- under a variety of conditions and can explain the effects of PGF(2alpha) on unidirectional 14C-labeled fluxes as a consequence of inhibition of H+ secretion to the apical bath, similar to what was previously suggested by our laboratory using a different methodological approach. The present method, utilizing radiolabeled HCO3-, may be useful as a means to evaluate the mechanism of action of hormones and drugs that may regulate acid-base homeostasis by altering proton and bicarbonate transport processes.


2012 ◽  
Vol 2 (1) ◽  
Author(s):  
R. Angelova

AbstractThe paper presents an experimental procedure developed for determination of the pore size, shape and distribution in a single layer woven fabric, for the construction of a virtual model to be incorporated in a future CFD software package. The procedure is based on non-destructive observation and analysis of woven samples. 14 different samples of gray fabrics of 100 % cotton in plain and twill weaves are investigated. The results obtained allow the creation of reality more realistic virtual model of the woven structure, and theoretical investigation of its porosity and permeability through computer simulation.


1934 ◽  
Vol 18 (1) ◽  
pp. 1-21 ◽  
Author(s):  
Victor Schechter

1. Direct galvanic current of 10 to 40 microamperes per square millimeter of cross-section of medium results in anodal determination of rhizoid origin in the differentiated cells of the red alga Griffithsia bornetiana. The current is most effective near the upper end of the range. 2. Within the range used there is an increase in the number of rhizoids produced with increase in current intensity and a decrease in size of rhizoids. 3. Currents of lower intensity require a longer time to produce these effects than comparatively high currents. 4. The orientation of the plants in the electrical field seems to affect the number of rhizoids produced, in that plants with apexes toward the anode produce more rhizoids. 5. Together with anodal rhizoid determination there is migration of chromatophores toward the anodal side of each cell. 6. Displacement of chromatophores (and other cytoplasmic bodies) by the centrifuge does not affect the point of rhizoid origin, but does affect the shoots. 7. Together with anodal determination of rhizoids the algal filaments become graded in color, from bright pink toward the cathode to pale tan toward the anode. 8. Evidence is presented to show that this is not due to a pH change, but to a loss of pigment by chromatophores toward the anode and electrophoresis of the pigment toward the cathode. 9. In conclusion the probability is pointed out that the current acts in morphogenesis by moving particles of different charge.


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