Imperial College London

DrRonnyPini

Faculty of EngineeringDepartment of Chemical Engineering

Reader in Chemical Engineering
 
 
 
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Contact

 

+44 (0)20 7594 7518r.pini Website

 
 
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Location

 

415ACE ExtensionSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@inproceedings{Yao:2018:10.2118/191540-ms,
author = {Yao, S and Pini, R and Wang, X and Zeng, F and Ju, N},
doi = {10.2118/191540-ms},
title = {Computational fluid dynamics modeling of slip flow coupled with gas adsorption/desorption kinetics in complex pore space},
url = {http://dx.doi.org/10.2118/191540-ms},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - CPAPER
AB - At reservoir conditions, gas flow confined in submicron pores of shale falls within slip flow and transition flow regimes. Beyond the common instant equilibrium assumption, we believe that gas adsorption/ desorption on rough pore surfaces could be in non-equilibrium status when gas pressure keeps decreasing during production. We investigate the interplay of gas slip flow inside complex submicron-scale pores and gas adsorption/desorption kinetics on pore surfaces with computational fluid dynamics (CFD) under unsteady-state flow conditions. Different from previous studies, the gas adsorption/desorption is in non-equilibrium state, which is closer to real reservoir conditions. Given pore pressure Pp at time t, linear driving force model with gas desorption rate coefficient kd is applied to describe the difference between the equilibrium adsorption amount (calculated with adsorption isotherms) and the actual adsorption amount per unit pore surface area. Free gas flow inside 3D reconstructions of shale pore space is modeled by Navier-Stokes equations with Maxwell's first-order slip boundary conditions. To include gas contributions from desorption, extra source with strength equal to the gas desorption rate is added to the slip boundaries. Any type of adsorption isotherms can be incorporated into our CFD modeling. We investigate the coupling of slip flow and Langmuir adsorption isotherms for methane in 3D reconstructed pore space. We observe that not all of adsorbed gas measured in adsorption isotherms contribute to gas production. In our study the pore pressure, Pp, decreases along with time t. One significant finding is that there exists a key time point, tk, after which adsorbed gas starts desorbing off pore surfaces and the decreasing rate of pore pressure becomes smaller. The higher the gas desorption rate coefficient, kd, is, the earlier tk occurs. But the decreasing rate of pore pressure is no longer sensitive to the coefficient, kd, when kd is larger than 0.0005.
AU - Yao,S
AU - Pini,R
AU - Wang,X
AU - Zeng,F
AU - Ju,N
DO - 10.2118/191540-ms
PY - 2018///
TI - Computational fluid dynamics modeling of slip flow coupled with gas adsorption/desorption kinetics in complex pore space
UR - http://dx.doi.org/10.2118/191540-ms
ER -