In this paper we report a small-angle neutron-scattering investigation of micelle formation by the fluorocarbon-hydrocarbon block copolymer, polyvinyl acetate-b-poly (1,1,2,2-tetrahydroperfluoro-octyl acrylate) in supercritical ${\mathrm{CO}}_2$ ${(\mathrm{s}\mathrm{c}\mathrm{C}\mathrm{O}}_2)$ at 313 K. At high pressure the copolymer is in a monomeric state with a random coil structure, while at low pressure the polymer forms spherical aggregates stable in a wide range of thermodynamic conditions. By profiling pressure, a sharp monomer-micelle transition is obtained due to the tuning of the solvating ability of ${\mathrm{scCO}}_2.$ We confirm the previous finding that this aggregate-monomer transition is driven by the gradual penetration of ${\mathrm{CO}}_2$ molecules toward the core of the aggregate and is critically related to the density of the solvent, thus giving additional support to the concept of a critical micellization density reported earlier on a similar polymer.

• Received 1 May 2000

DOI:https://doi.org/10.1103/PhysRevE.62.5839