Solvent Selectivity controls Micro- versus Macro-phase Separation in Multiblock Chains
arXiv:2405.12054 · doi:10.1021/acs.macromol.4c01214
Abstract
Monte Carlo simulations in the grand canonical ensemble were used to obtain critical parameters and conditions leading to microphase separation for block copolymers with solvophilic and solvophobic segments. Solvent selectivity was systematically varied to distinguish between systems that undergo macrophase separation to ones that microphase separate in the dilute phase, prior to macrophase separating. Finite-size scaling was used to obtain the critical parameters. Interestingly, corrections to scaling increase significantly for systems that form finite aggregates. The threshold value of solvent selectivity for aggregation was determined for symmetric diblock chains of varying length. The results indicate that long diblock copolymers form micelles in the dilute phase prior to macrophase separation, even in marginally selective solvents. The dependence of critical temperature on solvent selectivity was obtained for triblock, multiblock, and alternating chains. For highly selective solvents, strong structuring of both dilute and dense phases makes it harder to reach equilibrium.
References in corpus (6)
- Model for disordered proteins with strongly sequence-dependent liquid phase behavior
- Phase Equilibria of Lattice Polymers from Histogram Reweighting Monte Carlo Simulations
- Probability distribution of the order parameter for the 3D Ising model universality class: a high precision Monte Carlo study
- Crossover critical behavior in the three-dimensional Ising model
- Phase Separation and Aggregation in Multiblock Chains
- Sequence Dependence of Critical Properties for 2-letter Chains