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Miscible density fingering of chemical fronts in porous media: Nonlinear simulations

机译:多孔介质中化学前沿的混溶密度指法:非线性模拟

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Nonlinear interactions between chemical reactions and Rayleigh-Taylor type density fingering are studied in porous media or thin Hele-Shaw cells by direct numerical simulations of Darcy's law coupled to the evolution equation for the concentration of a chemically reacting solute controlling the density of miscible solutions. In absence of flow, the reaction-diffusion system features stable planar fronts traveling with a given constant speed v and width w. When the reactant and product solutions have different densities, such fronts are buoyantly unstable if the heavier solution lies on top of the lighter one in the gravity field. Density fingering is then observed. We study the nonlinear dynamics of such fingering for a given model chemical system, the iodate-arsenious acid reaction. Chemical reactions profoundly affect the density fingering leading to changes in the characteristic wavelength of the pattern at early time and more rapid coarsening in the nonlinear regime. The nonlinear dynamics of the system is studied as a function of the three relevant parameters of the model, i.e., the dimensionless width of the system expressed as a Rayleigh number Ra, the Damkohler number Da, and a chemical parameter d which is a function of kinetic constants and chemical concentration, these two last parameters controlling the speed v and width w of the stable planar front. For small Ra, the asymptotic nonlinear dynamics of the fingering in the presence of chemical reactions is one single finger of stationary shape traveling with constant nonlinear speed V>v and mixing zone W>w. This is drastically different from pure density fingering for which fingers elongate monotonically in time. The asymptotic finger has axial and transverse averaged profiles that are self-similar in unit lengths scaled by Ra. Moreover, we find that W/Ra scales as Da(-0.5). For larger Ra, tip splittings are observed. (C) 2004 American Institute of Physics. [References: 55]
机译:通过在达西定律的直接数值模拟中耦合化学反应溶质的浓度来控制可混溶溶液的密度,研究了多孔介质或薄Hele-Shaw池中化学反应与Rayleigh-Taylor型密度指法之间的非线性相互作用。在没有流动的情况下,反应扩散系统具有以给定的恒定速度v和宽度w行驶的稳定的平面前沿。当反应物溶液和产物溶液的密度不同时,如果在重力场中较重的溶液位于较轻的溶液的顶部,则这些前沿不稳定。然后观察到密度指法。对于给定的模型化学系统碘酸盐-亚砷酸反应,我们研究了这种指法的非线性动力学。化学反应深刻影响密度指法,从而导致图案的特征波长在早期发生变化,并在非线性状态下更快地变粗。根据模型的三个相关参数来研究系统的非线性动力学,即系统的无量纲宽度表示为瑞利数Ra,Damkohler数Da和化学参数d,后者是动力学常数和化学浓度,这两个最后的参数控制着稳定平面前沿的速度v和宽度w。对于小Ra,在存在化学反应的情况下,指法的渐近非线性动力学是一个固定形状的单指,以恒定的非线性速度V> v和混合区W> w传播。这与纯密度指法截然不同,后者的手指在时间上单调地伸长。渐近手指的轴向和横向平均轮廓在单位长度上由Ra缩放是自相似的。此外,我们发现W / Ra缩放为Da(-0.5)。对于较大的Ra,观察到尖端裂开。 (C)2004美国物理研究所。 [参考:55]

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