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Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery
Herein, a hyper-branched polymer h-PMAD with, simultaneously, surface activity, an anti-polyelectrolyte effect and a hydrophobic association was prepared via aqueous solution free radical polymerization, and characterized by IR, NMR, TG–DTG and SEM. The polymer h-PMAD provided excellent comprehensiv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064395/ https://www.ncbi.nlm.nih.gov/pubmed/35516380 http://dx.doi.org/10.1039/c9ra01554j |
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author | Wu, Qi Gou, Shaohua Huang, Jinglun Fan, Guijuan Li, Shiwei Liu, Mengyu |
author_facet | Wu, Qi Gou, Shaohua Huang, Jinglun Fan, Guijuan Li, Shiwei Liu, Mengyu |
author_sort | Wu, Qi |
collection | PubMed |
description | Herein, a hyper-branched polymer h-PMAD with, simultaneously, surface activity, an anti-polyelectrolyte effect and a hydrophobic association was prepared via aqueous solution free radical polymerization, and characterized by IR, NMR, TG–DTG and SEM. The polymer h-PMAD provided excellent comprehensive properties in terms of surface activity, thickening, water solubility, rheology and aging, which were compared with studies of HPAM and the homologous linear polymer PMAD. Specifically, the IFT value was 55.40 mN m(−1), 789.24 mPa s apparent viscosity with a dissolution time of 72 min, 97.72, 90.77 and 105.81 mPa s with Na(+), Ca(2+) and Mg(2+) of 20 000, 2000 and 2000 mg L(−1), respectively. Meanwhile, the non-Newtonian shear thinning behavior had a 96.33% viscosity retention while the shear rate went from 170 s(−1) to 510 s(−1) and then returned to 170 s(−1) again and 0.12 Hz curve, with an intersection frequency of G′ and G′′. Also, it had 33.51% and 50.96% viscosity retention in formation and deionized water at 100 °C and a low viscosity loss in formation water at 80 °C over 4 weeks. Moreover, the h-PMAD had an EOR of 11.61%, was obviously higher than PMAD with 8.19% and HPAM with 5.88%. Most importantly, the better EOR of h-PMAD over that of PMAD testified that the hyper-branched structure provided an active carrier for copolymers with functionalized monomers to exert greater effects in displacement systems, which is of an extraordinary meaning. |
format | Online Article Text |
id | pubmed-9064395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90643952022-05-04 Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery Wu, Qi Gou, Shaohua Huang, Jinglun Fan, Guijuan Li, Shiwei Liu, Mengyu RSC Adv Chemistry Herein, a hyper-branched polymer h-PMAD with, simultaneously, surface activity, an anti-polyelectrolyte effect and a hydrophobic association was prepared via aqueous solution free radical polymerization, and characterized by IR, NMR, TG–DTG and SEM. The polymer h-PMAD provided excellent comprehensive properties in terms of surface activity, thickening, water solubility, rheology and aging, which were compared with studies of HPAM and the homologous linear polymer PMAD. Specifically, the IFT value was 55.40 mN m(−1), 789.24 mPa s apparent viscosity with a dissolution time of 72 min, 97.72, 90.77 and 105.81 mPa s with Na(+), Ca(2+) and Mg(2+) of 20 000, 2000 and 2000 mg L(−1), respectively. Meanwhile, the non-Newtonian shear thinning behavior had a 96.33% viscosity retention while the shear rate went from 170 s(−1) to 510 s(−1) and then returned to 170 s(−1) again and 0.12 Hz curve, with an intersection frequency of G′ and G′′. Also, it had 33.51% and 50.96% viscosity retention in formation and deionized water at 100 °C and a low viscosity loss in formation water at 80 °C over 4 weeks. Moreover, the h-PMAD had an EOR of 11.61%, was obviously higher than PMAD with 8.19% and HPAM with 5.88%. Most importantly, the better EOR of h-PMAD over that of PMAD testified that the hyper-branched structure provided an active carrier for copolymers with functionalized monomers to exert greater effects in displacement systems, which is of an extraordinary meaning. The Royal Society of Chemistry 2019-05-24 /pmc/articles/PMC9064395/ /pubmed/35516380 http://dx.doi.org/10.1039/c9ra01554j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wu, Qi Gou, Shaohua Huang, Jinglun Fan, Guijuan Li, Shiwei Liu, Mengyu Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
title | Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
title_full | Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
title_fullStr | Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
title_full_unstemmed | Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
title_short | Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
title_sort | hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064395/ https://www.ncbi.nlm.nih.gov/pubmed/35516380 http://dx.doi.org/10.1039/c9ra01554j |
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