Gelation of Poly(Vinylidene Fluoride) Solutions in Native and Organically Modified Silica Nanopores

Abstract

The purpose of this study is to highlight the surface and size effects of the nanopores on the thermodynamics and kinetics of gelation. The effects have been probed by applying differential scanning calorimetry to poly(vinylidene fluoride) solutions in tetraethylene glycol dimethyl ether (tetraglyme) and γ-butyrolactone. Nanoconfinement has been accomplished by introducing gels into native and organically modified silica nanopores (4–30 nm). Nanoconfinement has produced two major effects. First, the heat of gelation has decreased three to four times compared to that for the bulk systems. Second, the temperature of gelation has increased by ~40 °C (tetraglyme based systems) and ~70 °C (γ-butyrolactone based systems), the increase being stronger in native nanopores. The effects are discussed in terms of acceleration of gelation due to heterogeneous nucleation at the confining surface, and retardation of gelation due to constricted polymer chain mobility in the middle of the pore volume. Calorimetric data have been subjected to isoconversional kinetics analysis. The obtained temperature dependencies of the activation energies of gelation have been interpreted in the frameworks of the nucleation model of Turnbull and Fisher. The results suggest that nanoconfinement leads to a lowering of both the free energy of nucleation and activation energy of diffusion.