4.2 Article

Solubility Behavior of Amphiphilic Block and Random Copolymers Based on 2-Ethyl-2-oxazoline and 2-Nonyl-2-oxazoline in Binary Water-Ethanol Mixtures

Journal

Publisher

WILEY
DOI: 10.1002/pola.23168

Keywords

amphiphilic copolymers; LCST; micelles; polyamides; poly(2-oxazoline); self-organization; solution properties; UCST; water-ethanol

Funding

  1. Dutch Polymer Institute (DPI) [500, 543]
  2. NWO
  3. Fonds der Chemischen Industrie
  4. Politique Scientifique Federale
  5. Interuniversity Attraction Poles Programme [PAI VI/27]

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The solution properties of random and block copolymers based on 2-ethyl-2-oxazoline (EtOx) and 2-nonyl-2-oxazoline (NonOx) were investigated in binary solvent mixtures ranging from pure water to pure ethanol. The solubility phase diagrams for the random and block copolymers revealed solubility (after beating), insolubility, dispersions, micellization as well as lower critical solution temperature (LCST) and upper critical solution temperature behavior. The random and block copolymers containing over 60 mol % pNonOx were found to be solubilized in ethanol upon heating, whereas the dissolution temperature of the block copolymers was found to be much higher than for the random copolymers due to the higher extent of crystallinity. Furthermore, the block copolymer containing 10 mol % pNonOx exhibited a LCST in aqueous solution at 68.7 degrees C, whereas the LCST for the random copolymer was found to be only 20.8 degrees C based on the formation of hydrophobic micro-domains in the block copolymer. The random copolymer displayed a small increase in LCST up to a solvent mixture of 9 wt % EtOH, whereas further increase of ethanol led to a decrease in LCST, which is probably due to the water-breaking effect causing an increased attraction between ethanol and the hydrophobic part of the copolymer. In addition, the EtOx-NonOx block copolymers revealed the formation of micelles and dynamic light scattering demonstrated that the micellar size is increasing with increasing the ethanol content due to the enhanced solubility of EtOx. (C) 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 515-522, 2009

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