Journal
JOURNAL OF APPLIED POLYMER SCIENCE
Volume 129, Issue 4, Pages 2057-2062Publisher
WILEY-BLACKWELL
DOI: 10.1002/app.38914
Keywords
colloids; ionic liquids; micelles; surfaces and interfaces; surfactants
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Funding
- National Science and Technology fund major project of P.R.C. [2008ZX05011]
- Heilongjiang Province Natural Science Foundation [ZJG0507]
- Youth Fund of Heilongjiang Province Natural Science Foundation [QC08C33]
- Graduate funding innovative research in Heilongjiang Province [YJSCX2008-044HLJ]
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The drop volume method was used to determine the surface tensions of two series of polymerizable ionic liquid surfactants, namely, 1-acryloyloxypropyl-3-alkylimidazolium chloride [APCnim][Cl] (n = 8, 10, 12) containing two hydrophobic tail chains and 1-propionyloxypropyl-3-alkylimidazolium chloride [PPCnim][Cl] (n = 8, 10, 12), which showed similar structures with [APCnim][Cl] (n = 8, 10, 12) at 25 degrees C. The surface properties of the surfactants were also compared. Furthermore, the thermodynamic behavior of [PPCnim][Cl] (n = 10, 12, 14) micellization in aqueous solution and the enthalpyentropy compensation phenomenon were studied. The two kinds of surfactants had high surface activity. Double bonds had almost no effect on the surface properties of [APCnim][Cl]. The micellization of [PPCnim][Cl] in aqueous solution was spontaneous and entropy-driven. For the surfactant with specific structure, micellization ability initially increased and then decreased with temperature increase. The entropic contribution to Gibbs free energy change tended to decrease, whereas the enthalpic contribution increased. In addition, the enthalpyentropy compensation phenomenon occurred during the micellization process. For all [PPCnim][Cl], the compensation temperature was (314 +/- 1) K, which remained unaffected by the surfactant molecular structure. However, when the hydrophobic carbon chain length increased, both micelle formation ability and stability increased. (c) 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013
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