Dynamic analysis of viscous flow and diffusion in porous solids

AIChE Journal ◽  
1989 ◽  
Vol 35 (8) ◽  
pp. 1370-1375 ◽  
Author(s):  
Gülşen Do??u ◽  
Ahmet Pekediz ◽  
Timur Do??u
Nature ◽  
1962 ◽  
Vol 195 (4840) ◽  
pp. 482-483 ◽  
Author(s):  
F. A. L. DULLIEN
Keyword(s):  

2013 ◽  
Vol 2013.21 (0) ◽  
pp. _409-1_-_409-3_
Author(s):  
Fumihiro WAKAI ◽  
Yutaka SHINODA ◽  
Takashi AKATSU ◽  
Kenneth Brakke

1971 ◽  
Vol 42 (11) ◽  
pp. 4183-4187 ◽  
Author(s):  
R. A. Pasternak ◽  
M. V. Christensen

1992 ◽  
Vol 46 (17) ◽  
pp. 10701-10705 ◽  
Author(s):  
M. Y. Lin ◽  
B. Abeles ◽  
J. S. Huang ◽  
H. E. Stasiewski ◽  
Q. Zhang
Keyword(s):  

2005 ◽  
Vol 899 ◽  
Author(s):  
Sergey Vasenkov ◽  
Jörg Kärger

AbstractPulsed field gradient (PFG) NMR technique has been applied to study molecular transport in two different types of nanostructured materials, viz. in fluid catalytic cracking (FCC) catalysts and in lipid membranes. Diffusion studies have been performed for a broad range of molecular displacements covering displacements that are as small as a fraction of a micron. The effective diffusivities recorded on various length scales are used to evaluate the relevance of various transport modes in the particles of FCC catalysts for the rate of molecular exchange between catalyst particles and the surrounding atmosphere. This rate is shown to be primarily related to the diffusion in the meso- and macropores of the particles under the condition of fast molecular exchange between these pores and the zeolite crystals located in the particles. Studies of lipid membranes are focused on developing fundamental understanding of the influence of various types of domains on lateral mobility of lipids. A meaningful study of this influence requires an ability of monitoring lipid diffusion for different displacements that are smaller and larger than the domain size. First PFG NMR data along this direction are presented.


1942 ◽  
Vol 15 (3) ◽  
pp. 537-544 ◽  
Author(s):  
Richard M. Barrer

Abstract Some properties of flow of solutes in and through rubbers are outlined. These properties indicate that, due to fluctuations of thermal energy, activated zones exist in certain polymers, of which viscous flow and diffusion are a consequence. A simple statistics of activated zones has been given, and from it equations are obtained for ΣN, D, Ds, and η, denoting respectively the total number of activated zones in rubber, the diffusion constant of simple solutes in the polymer, the self-diffusion constant of rubber, and its viscosity. Functional relations are predicted between log Do, log ηo, or ΔS* (the entropy of activation) and the Arrhenius energy of activation for diffusion or viscous flow. The available data clearly demonstrate this relationship. They also indicate no discontinuity between rubbers and liquids as diffusion media.


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