Characterization, Solution Behavior, and Microstructure of a Hydrophobically Associating Nonionic Copolymer
To obtain an oil-displacement polymer with good thermal stability and solution properties, self-assembling acrylamide (AM)/4-butylstyrene (BST) copolymers (PSA) were synthesized by the micellar copolymerization technique. The resulting polymer was characterized by elemental analysis and UV and FT-IR...
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Veröffentlicht in: | Journal of solution chemistry 2008-09, Vol.37 (9), p.1227-1243 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To obtain an oil-displacement polymer with good thermal stability and solution properties, self-assembling acrylamide (AM)/4-butylstyrene (BST) copolymers (PSA) were synthesized by the micellar copolymerization technique. The resulting polymer was characterized by elemental analysis and UV and FT-IR spectroscopy. Conventional DSC measurement was used successfully to characterize the hydrophobic microblock structure of PSA, and two glass transition temperatures were found in the polymer: at 203 °C for the AM segments and at 106 °C for the hydrophobic BST segments. The initial decomposition temperature (234 °C) of the polymer is higher than that of polyacrylamide (210 °C). The DSC and TG results suggest that incorporation of BST into PSA enhances the molecular rigidity and thermal stability of the polymer. The apparent viscosity of a PSA solution greatly depends on the amount of BST in the polymer, and the polymer exhibits salt-thickening, temperature-thickening, thixotropy, pseudo-plastic behavior, anti shearing, and good anti-aging properties at 80 °C. In addition, the apparent viscosities of PSA solutions are increased remarkably by the addition of a small amount of surfactant. AFM measurements show that large block-like aggregates and small compact aggregates are formed in aqueous solutions of 0.4 g⋅dL
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PSA because of strong intermolecular hydrophobic associations, despite the low molecular weight, and their sizes increase upon addition of a small amount of salt. |
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ISSN: | 0095-9782 1572-8927 |
DOI: | 10.1007/s10953-008-9309-8 |