Hierarchies of nonclassical reaction kinetics due to anisotropic confinements

被引:16
作者
Ahn, J [1 ]
Kopelman, R
Argyrakis, P
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[3] Univ Thessaloniki, Dept Phys, GR-54006 Salonika, Greece
关键词
D O I
10.1063/1.477820
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In contrast to classical chemical reaction kinetics, for diffusion limited chemical reactions the anisotropy of the geometry has far reaching effects. We use tubular two and three-dimensional spaces to illustrate and discuss the dimensional crossover in A + B --> 0 reactions due to dimensional compactification. We find that the crossover time t(c) = W-alpha scales as alpha = beta/(a - b), where a, b, and beta are given by the earlier and the late time inverse density scaling of rho(-1) similar to t(a) and rho(-1) similar to t(b)W(beta), respectively. We also obtain a critical width W-c below (above) which the chemical reaction progresses without (with) traversing a two or three-dimensional Ovchinnikov-Zeldovich (OZ) reaction regime. As a result we find that there exist different hierarchies of dimensionally forced crossovers, depending on the initial conditions and geometric restrictions. Kinetic phase diagrams are employed, and exponents are given for various Euclidean and fractal compactified geometries, for the A + B and A + A elementary reactions. Monte Carlo simulations illustrate some of the kinetic hierarchies. (C) 1999 American Institute of Physics. [S0021-9606(99)00504-8].
引用
收藏
页码:2116 / 2121
页数:6
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