Effect of Solvent Selectivity on Chain Exchange Kinetics in Block Copolymer Micelles
ORAL
Abstract
Block copolymer (BCP) micelles in selective solvents are useful for a variety of applications, such as nanolithography, drug delivery, and viscosity modification. The solvent quality is an important factor for both thermodynamics and dynamics of BCP micelles. Previous work revealed the effect of solvent selectivity on thermodynamic properties of BCP micelles formed by poly(styrene-b-ethylene-alt-propylene) (PS-PEP) diblock copolymers in mixed solvents of squalane and 1-phenyldodecane. The systematic change of solvent composition tunes the interfacial tension between the core and corona-solvent matrix, embodied in the Flory-Huggins interaction parameter χ. This should also affect the kinetics of chain exchange between micelles. This presentation will describe the consequences of varying the solvent composition on the rate of chain exchange using time-resolved small-angle neutron scattering (TR-SANS). An independent method, static light scattering (SLS), was performed to estimate χ between the core block and the solvent as a function of solvent composition and temperature. Based on TR-SANS and SLS results, the dependence of the chain exchange rate on χ can be quantified.
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Presenters
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En Wang
- University of Minnesota