A new approach for quantitative mapping of retention mechanisms of associative polymers in porous media
被引:2
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作者:
Afolabi, Richard O.
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Robert Gordon Univ, Sch Engn, Petr Engn Res Grp PERG, Aberdeen AB10 7GJ, ScotlandRobert Gordon Univ, Sch Engn, Petr Engn Res Grp PERG, Aberdeen AB10 7GJ, Scotland
Afolabi, Richard O.
[1
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Oluyemi, Gbenga F.
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Robert Gordon Univ, Sch Engn, Petr Engn Res Grp PERG, Aberdeen AB10 7GJ, ScotlandRobert Gordon Univ, Sch Engn, Petr Engn Res Grp PERG, Aberdeen AB10 7GJ, Scotland
Oluyemi, Gbenga F.
[1
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Officer, Simon
[2
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Ugwu, Johnson O.
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机构:
Teesside Univ, Sch Sci Engn & Design, Middlesbrough TS1 3BX, Cleveland, EnglandRobert Gordon Univ, Sch Engn, Petr Engn Res Grp PERG, Aberdeen AB10 7GJ, Scotland
Ugwu, Johnson O.
[3
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机构:
[1] Robert Gordon Univ, Sch Engn, Petr Engn Res Grp PERG, Aberdeen AB10 7GJ, Scotland
[2] Robert Gordon Univ, Sch Pharm & Life Sci, Aberdeen AB10 7GJ, Scotland
The retention of associative polymer molecules poses a significant challenge for its transport in porous media, and this arises due to the hydrophobic interactions that exists between the retained molecules. The known experimental approach in literature for quantifying polymer retention under static or dynamic conditions reports a generalized outcome without adequate estimates for each type of retention mechanisms. Thus, an accurate quantitative description of the various retention mechanisms (monolayer adsorption, multilayer adsorption and entrapment) attributable to associative polymers is crucial for proper optimization of its transport in porous media. In this work, a novel predictive approach was developed for quantitative mapping of the various retention mechanisms connected with associative polymers. The basis was a first-principles method adopted in mapping static to dynamic retention. This novel approach was achieved by relating the characteristic time scale for static and dynamic retention to the variation in polymer and reservoir properties, thus making it possible to correlate static retention results to large-scale dynamic retention with minimal fitting parameters. Furthermore, the mapping of the static to dynamic retention ensured an accurate quantification of the different retention mechanisms attributable to associative polymers. In this model, the in-situ entrapment was linked to the effective pore radius and the hydrodynamic size of the polymer molecules. Entrapment of polymer molecular aggregates was predicted based on the assumption that this occurs when the hydrodynamic size of the molecules becomes equal/greater than the effective pore size in the porous media. In addition, a threshold concentration value was estimated from which mechanical entrapment of polymer molecules would occur in a porous media alongside adsorption on pore surface. Similarly, a concentration value was estimated at which entrapment of polymer molecules becomes the dominant retention mechanism in the porous media. (C) 2021 Elsevier B.V. All rights reserved.
机构:
King Fahd Univ Petr & Minerals, Coll Petr & Geosci, Dept Petr Engn, Dhahran, Saudi Arabia
King Fahd Univ Petr & Minerals, Ctr Integrat Petr Res, Dhahran, Saudi ArabiaUniv Alberta, Sch Min & Petr, Dept Civil & Environm Engn, Edmonton, AB, Canada
机构:
New Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USANew Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
Seright, R. S.
Fan, Tianguang
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机构:New Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
Fan, Tianguang
Wavrik, Kathryn
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机构:New Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
Wavrik, Kathryn
Wan, Hao
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机构:New Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
Wan, Hao
Gaillard, Nicolas
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机构:
SNF Floerger, R&D Project, Andrezieux, FranceNew Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
Gaillard, Nicolas
Favero, Cedrick
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机构:New Mexico Inst Min & Technol, New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
机构:
Univ Fed Rio Grande do Norte, Dept Engn Quim, BR-59078970 Natal, RN, BrazilUniv Fed Rio Grande do Norte, Dept Engn Quim, BR-59078970 Natal, RN, Brazil
Santos, A.
Barros, P. H. L.
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Univ Fed Rio Grande do Norte, Pos Grad Engn Petr, BR-59078970 Natal, RN, BrazilUniv Fed Rio Grande do Norte, Dept Engn Quim, BR-59078970 Natal, RN, Brazil
机构:
Islamic Azad Univ, North Tehran Branch, Young Researchers & Elites Club, Tehran, IranSharif Univ Technol, Dept Chem & Petr Engn, Tehran, Iran
Arabloo, Milad
Shokrollahi, Amin
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Islamic Azad Univ, North Tehran Branch, Young Researchers & Elites Club, Tehran, IranSharif Univ Technol, Dept Chem & Petr Engn, Tehran, Iran
Shokrollahi, Amin
Mohammadi, Amir H.
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机构:
IRGCP, Paris, France
Univ KwaZulu Zatal, Sch Engn, Thermodynam Res Unit, Durban, South AfricaSharif Univ Technol, Dept Chem & Petr Engn, Tehran, Iran