A Forming of Microscopic Diffusion Flames with Molecular Diffusion Effects by Double Micro-Flames

2000 ◽  
Vol 2000.1 (0) ◽  
pp. 777-778
Author(s):  
Tamio IDA
2008 ◽  
Vol 22 (1) ◽  
pp. 278-283 ◽  
Author(s):  
Jeong Soo Kim ◽  
Jeong Park ◽  
Oh Boong Kwon ◽  
Jin Han Yun ◽  
Sang In Keel ◽  
...  

1995 ◽  
Vol 7 (8) ◽  
pp. 1999-2007 ◽  
Author(s):  
A. R. Kerstein ◽  
M. A. Cremer ◽  
P. A. McMurtry

Geophysics ◽  
2015 ◽  
Vol 80 (2) ◽  
pp. E41-E47 ◽  
Author(s):  
Zhi-Xiang Luo ◽  
Jeffrey Paulsen ◽  
M. Vembusubramanian ◽  
Yi-Qiao Song

The 2D nuclear magnetic resonance diffusion-relaxation experiment (NMR [Formula: see text]) has proven to be a powerful method to characterize complex fluids. Molecular components with distinct diffusion coefficients are shown on [Formula: see text] maps as separate peaks. In porous media such as reservoir rocks, molecular diffusion is restricted such that the apparent diffusion coefficient is time dependent and the diffusion behavior is non-Gaussian. Such restricted diffusion effects can manifest on the [Formula: see text] maps and complicate the interpretation of the results, but so far, they have not been systematically investigated. We used controlled laboratory experiments to demonstrate the influence of non-Gaussian restricted diffusion on NMR [Formula: see text] maps under various conditions and to show how restricted diffusion effects on [Formula: see text] maps can be distinguished from multiphase fluids. NMR [Formula: see text] experiments were carried out on a series of water-saturated packs of glass beads and two rock cores. The results revealed the important role of two critical length scales controlling the restricted diffusion effects on NMR [Formula: see text] maps: the molecular diffusion length [Formula: see text] during the NMR diffusion encoding time and the characteristic pore size [Formula: see text]. For [Formula: see text], the effect of non-Gaussian diffusion was negligible and the NMR [Formula: see text] map showed only one peak. As [Formula: see text] approaches [Formula: see text], an additional peak with a smaller diffusion coefficient emerged (resembling the [Formula: see text] map of an unrestricted two molecular components fluid), and its relative intensity was maximized (to [Formula: see text]), when [Formula: see text]. As [Formula: see text] further increased, the relative intensity of the additional peak started decreasing, in contrast to the scenario of [Formula: see text] maps of multiphase fluids. We determined the extent and influence of restricted diffusion on NMR [Formula: see text] maps, and we informed the interpretation of NMR [Formula: see text] measurements, which are commonly used to quantify gas, water, and oil signals in reservoir rocks.


Author(s):  
Zakirul Haque ◽  
John P. Barton

This paper involves a theoretical analysis of the propagation of sound within chemically reacting hydrocarbon combustion products. A new procedure for determining the sound speed and absorption coefficient was developed. Using a similar approach can do analyses for other chemically reacting gas mixture. One-dimensional sound propagation was assumed. Molecular diffusion effects, such as viscous stress, heat conduction, and mass diffusion were appropriately neglected along with possible effects due to vibrational non-equilibrium. In this way only the effects of chemical reactions on sound propagation was considered. The expressions for sound speed and absorption coefficient were derived as a function of frequency.


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