Model development for diffusion with instantaneous chemical reactions in a spherical multicomponent drop

1995 ◽  
Vol 12 (5) ◽  
pp. 551-556
Author(s):  
Byeong-Il Non ◽  
Byung-Hyun Moon ◽  
Tae-Kyung Yoon ◽  
Jong-Hyun Kim
1991 ◽  
Vol 02 (01) ◽  
pp. 430-436
Author(s):  
ELAINE S. ORAN ◽  
JAY P. BORIS

This paper describes model development and computations of multidimensional, highly compressible, time-dependent reacting on a Connection Machine (CM). We briefly discuss computational timings compared to a Cray YMP speed, optimal use of the hardware and software available, treatment of boundary conditions, and parallel solution of terms representing chemical reactions. In addition, we show the practical use of the system for large-scale reacting and nonreacting flows.


1995 ◽  
Vol 12 (1) ◽  
pp. 18-22 ◽  
Author(s):  
Byeong Il Noh ◽  
Tae Kyung Yoon ◽  
Byung Hyun Moon ◽  
Jong Hyun Kim

2004 ◽  
Vol 38 (1) ◽  
pp. 31-40 ◽  
Author(s):  
S. Yu. Shalunova ◽  
Yu. A. Pisarenko ◽  
A. S. Shuvalov ◽  
L. A. Serafimov

Author(s):  
H.H. Rotermund

Chemical reactions at a surface will in most cases show a measurable influence on the work function of the clean surface. This change of the work function δφ can be used to image the local distributions of the investigated reaction,.if one of the reacting partners is adsorbed at the surface in form of islands of sufficient size (Δ>0.2μm). These can than be visualized via a photoemission electron microscope (PEEM). Changes of φ as low as 2 meV give already a change in the total intensity of a PEEM picture. To achieve reasonable contrast for an image several 10 meV of δφ are needed. Dynamic processes as surface diffusion of CO or O on single crystal surfaces as well as reaction / diffusion fronts have been observed in real time and space.


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