Microscale Chaotic Mixing as a Driver for Chemical Reactions in Porous Media

被引:2
|
作者
Sanquer, Hugo [1 ]
Heyman, Joris [1 ]
Hanna, Khalil [2 ]
Le Borgne, Tanguy [1 ]
机构
[1] Univ Rennes, Geeosci Rennes, UMR CNRS 6118, F-35042 Rennes, France
[2] Univ Rennes, Ecole Natl Super Chim, UMR CNRS 6226, F-35708 Rennes, France
基金
欧洲研究理事会;
关键词
reactive transport; mixing-limited reactions; 3D imaging; chaotic mixing; redox reactions; RIM; LIF; PDMS; BIMOLECULAR REACTIONS; REACTION-KINETICS; TRANSPORT; DISPERSION; FRONTS; PORE; FLOW;
D O I
10.1021/acs.est.3c09749
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Mixing-induced reactions play a key role in a large range of biogeochemical and contaminant transport processes in the subsurface. Fluid flow through porous media was recently shown to exhibit chaotic mixing dynamics at the pore scale, enhancing microscale concentration gradients and controlling mixing rates. While this phenomenon is likely ubiquitous in environmental systems, it is not known how it affects chemical reactions. Here, we use refractive index matching and laser-induced fluorescence imaging of a bimolecular redox reaction to investigate the consequence of pore scale chaotic mixing on the reaction rates. The overestimation of measured reaction rates by the classical macrodispersion model highlights the persistence of incomplete mixing on the pore scale. We show that the reaction product formation is controlled by microscale chaotic mixing, which induces an exponential increase of the mixing interface and of the reaction rates. We derive a reactive transport model that captures experimental results and predicts that chaotic mixing has a first order control on reaction rates across a large range of time scales and P & eacute;clet and Damk & ouml;hler numbers. These findings provide a new framework for understanding, assessing, and predicting mixing-induced reactions and their role on the fate and mobility of environmental compounds in natural porous media.
引用
收藏
页码:8899 / 8908
页数:10
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