Molecular tailoring of thermoreversible copolymer gels: Some new mechanistic insights

Journal Article (Journal Article)

We earlier reported the role of hydrophobic and hydrogen bonding interactions on the transition temperatures of thermoreversible copolymer gels. We show here that the chemical structure of the hydrophobe and its concentration determine the transition temperatures [lower critical solution temperature (LCST)] and the heat of transition of new hydrophobically modified poly(N-isopropyl acrylamide) [PNIPAm] copolymer gels. The gels, prepared by copolymerizing NIPAm monomer with hydrophobic comonomers containing increasing lengths of alkyl side groups and a terminal carboxyl acid group, showed lower LCST and lower heat of transition when compared to pure PNIPAm gel. The experimental results were also compared with theoretical calculations based on a lattice-fluid-hydrogen-bond [LFHB] model. We show experimentally and theoretically that a linear correlation exists between the transition temperature and length of the hydrophobic alkyl side group. Also, in apparent contradiction to previous work, we found a reduction in the heat of transition with increasing hydrophobicity. We propose that the presence of the terminal carboxyl acid group on the hydrophobic side chain of the comonomer prevents the association of water molecules around the hydrophobe, thereby causing a reduction in the heat of transition. The LFHB model supports this argument. © 1998 American Institute of Physics.

Full Text

Duke Authors

Cited Authors

  • Badiger, MV; Lele, AK; Bhalerao, VS; Varghese, S; Mashelkar, RA

Published Date

  • December 1, 1998

Published In

Volume / Issue

  • 109 / 3

Start / End Page

  • 1175 - 1184

International Standard Serial Number (ISSN)

  • 0021-9606

Digital Object Identifier (DOI)

  • 10.1063/1.476663

Citation Source

  • Scopus