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               <dc:title>Linking mixing interface deformation to concentration gradients in porous media</dc:title>
               <dc:creator>Farhat, Saif</dc:creator>
               <dc:creator>Bolster, Diogo</dc:creator>
               <dc:creator>Solé Marí, Guillem</dc:creator>
               <dc:subject>Àrees temàtiques de la UPC::Matemàtiques i estadística::Anàlisi numèrica::Mètodes numèrics</dc:subject>
               <dc:subject>Chemical kinetics</dc:subject>
               <dc:subject>dynamics &amp; catalysis</dc:subject>
               <dc:subject>Contact line dynamics</dc:subject>
               <dc:subject>Convection in porous media</dc:subject>
               <dc:subject>Granular mixing</dc:subject>
               <dc:subject>Laminar flows</dc:subject>
               <dc:subject>Laminar reacting flows</dc:subject>
               <dc:subject>Microfluidics</dc:subject>
               <dc:subject>Mixing enhancement</dc:subject>
               <dc:subject>Mixing in geophysical flows</dc:subject>
               <dc:subject>Scaling laws of complex systems</dc:subject>
               <dc:subject>Shear flows</dc:subject>
               <dc:subject>Stratified geophysical flows</dc:subject>
               <dc:description>We study the pore-scale transport of a conservative scalar forming an advancing mixing front, which can be re-interpreted to predict instantaneous mixing-limited bimolecular reactions. We investigate this using a set of two-dimensional, high-resolution numerical simulations within a poly-disperse granular porous medium, covering a wide range of Péclet (Pe) numbers. The aim is to show and exploit the direct link between pore-scale concentration gradients and mixing interface (midpoint concentration isocontour). We believe that such a perspective provides a complementary new lens to better understand mixing and spreading in porous media. We develop and validate a theoretical model that quantifies the temporal elongation of the mixing interface and the upscaled reaction kinetics in mixing-limited systems accounting for pore-scale concentration fluctuations. Contrary to the classical belief that, given sufficient time, pore-scale fluctuations would eventually be washed out, we show that for Pe>1 advection generates pore-scale concentration fluctuations more rapidly than they can be fully dissipated. For such Péclet numbers, once incomplete mixing is established, it will persist indefinitely. We identify critical Péclet thresholds (Pe=18 for Poiseuille flow, Pe=48 for porous media) where reaction efficiency is minimized. Finally, our developed model accurately reproduces the reaction product mass in a three-dimensional porous media column over a wide range of Péclet numbers, demonstrating its applicability to more realistic systems.</dc:description>
               <dc:description>This research was funded by National Science Foundation Grant No. EAR2049688 and by the European Commission (MixUp, MSCA-101068306). The authors gratefully acknowledge the Center for Research Computing (CRC) at the University of Notre Dame for providing the computational resources used to conduct the simulations in this work.</dc:description>
               <dc:description>Peer Reviewed</dc:description>
               <dc:description>Postprint (author's final draft)</dc:description>
               <dc:date>2025-02-14</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>https://journals.aps.org/prfluids/abstract/10.1103/PhysRevFluids.10.024501</dc:relation>
               <dc:rights>Open Access</dc:rights>
               <dc:publisher>American Physical Society (APS)</dc:publisher>
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