Solvent Selectivity controls Micro- versus Macro-phase Separation in Multiblock Chains

TL;DR

This study uses Monte Carlo simulations to explore how solvent selectivity influences micro- versus macro-phase separation in multiblock copolymers, revealing critical thresholds and behaviors across different chain architectures.

Contribution

It systematically analyzes the effect of solvent selectivity on phase separation modes in multiblock chains, providing critical parameters and insights into aggregation behavior.

Findings

Long diblock copolymers form micelles before macrophase separation.

Critical temperature depends on solvent selectivity for various chain types.

Highly selective solvents induce strong structuring, complicating equilibrium attainment.

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.