β‐Cyclodextrin‐functionalized copolymers based on multiple intermolecular forces for enhanced oil recovery
As one of mature enhanced oil recovery (EOR) technologies, polymer flooding has been extensively applied in oilfield. In this study, new hydrophobically associative copolymers were synthesized by free‐radical polymerization of acrylamide (AM), acrylic acid (AA), vinyl‐modified β‐cyclodextrins, and a...
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Published in | Polymer engineering and science Vol. 60; no. 10; pp. 2581 - 2592 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.10.2020
Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | As one of mature enhanced oil recovery (EOR) technologies, polymer flooding has been extensively applied in oilfield. In this study, new hydrophobically associative copolymers were synthesized by free‐radical polymerization of acrylamide (AM), acrylic acid (AA), vinyl‐modified β‐cyclodextrins, and a water‐soluble hydrophobic macromonomer (AA‐APE‐20). Fourier transform infrared, proton‐nuclear magnetic resonance, and scanning electron microscopy verified the structure of hydrophobically associative polymers (HDAPAMs). Compared with partially hydrolyzed polyacrylamide (HPAM), multiple intermolecular forces including chelation between ethoxyl (EO) group and Ca2+/Mg2+, electrostatic bridges between EO groups and carboxyl groups (COO−), hydrogen bonding between EO groups and AM groups (CONH2), hydrophobic association among nonyl phenol groups, and host‐guest inclusion interaction endowed HDAPAMs favorable temperature‐resistance, salt‐resistance, and displacement efficiency. It was found that HDAPAMs showed evident temperature‐response, salt thickening effect, favorable thixotropy, and viscoelasticity. Compared with HPAM, the core flooding experiments demonstrated that HDAPAMs could further enhance 6.97% to 8.43% oil recovery, even after HPAM flooding used. All the results revealed the EOR potential in HDAPAMs flooding. |
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ISSN: | 0032-3888 1548-2634 |
DOI: | 10.1002/pen.25496 |