Simultaneous sorption and mechanical entrapment during polymer flow through porous media

Journal Article (2016)
Author(s)

Rouhollah Farajzadeh (TU Delft - Reservoir Engineering, Shell Global Solutions International B.V.)

P. Bedrikovetsky (University of Adelaide)

Mohammad Lotfollahi (The University of Texas at Austin)

L. W. Lake (The University of Texas at Austin)

Research Group
Reservoir Engineering
Copyright
© 2016 R. Farajzadeh, P. Bedrikovetsky, M. Lotfollahi, L. W. Lake
DOI related publication
https://doi.org/10.1002/2015WR017885
More Info
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Publication Year
2016
Language
English
Copyright
© 2016 R. Farajzadeh, P. Bedrikovetsky, M. Lotfollahi, L. W. Lake
Research Group
Reservoir Engineering
Issue number
3
Volume number
52
Pages (from-to)
2279-2298
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Abstract

Physical adsorption and mechanical entrapment are two major causes of polymer retention in porous media. Physical adsorption is considered an equilibrium process and is often modeled by assuming a Langmuir isotherm. The outcome is a steady state pressure response because the permeability reduction is also accounted for by adsorption. However, some experimental data show gradual increase of pressure with time, implying that polymer retention is a time-dependent process. We discuss simultaneous effect of sorption and mechanical entrapment on the polymer retention in porous media. An exact solution for 1-D flow problem for the case of constant filtration coefficient and Langmuir-sorption isotherm, including explicit formulae for breakthrough concentration and pressure drop across the core is derived. The general model with a varying filtration coefficient was successfully matched with experimental data confirming the occurrence of simultaneous sorption with deep-bed filtration during polymer flow in porous media. In the absence of mechanical entrapment, the physical adsorption causes delay in the polymer front and does not affect the polymer concentration behind the front. Addition of mechanical entrapment results in slow recovery of the injected concentration at the outlet (for a varying filtration coefficient) or reaching to a steady state concentration, which is only a fraction of the injected concentration (for a constant filtration coefficient). Accurate assessment and quantification of the polymer retention requires both pressure and effluent concentration data at the outlet of the porous medium.

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