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Temperature dependence of micelle shape transitions in copolymer solutions: the role of inter-block incompatibility

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posted on 2024-05-03, 15:07 authored by Martin GreenallMartin Greenall, Matthew Derry

The nature of the transition between worm-like and spherical micelles in block copolymer dispersions varies between systems. In some formulations, heating drives a transition from worms to spheres, while in other systems the same transition is induced by cooling. In addition, a sphere-worm interconversion can be accompanied either by an increase or a decrease in the core solvation, even if the direction of the temperature dependence is the same. Here, self-consistent field theory is used to provide a potential explanation of this range of behaviour. Specifically, we show that, within this model, the dependence of the transition on the incompatibility  chi_{BS} of the solvophobic block B and the solvent S (the parameter most closely related to the temperature) is strongly influenced by the incompatibility chi_{AB} between B and the solvophilic block A. When chi_{AB} is small (chi_{AB} ≤ 0.1), it is found that increasing chi_{BS} produces a transition from worm-like micelles to spheres (or, more generally, from less curved to more curved structures). When chi_{AB} is above 0.1, increasing chi_{BS} drives the system from spheres to worm-like micelles. Whether a transition is observed within a realistic range of chi_{BS} is also found to depend on the fraction of solvophilic material in the copolymer. The relevance of our calculations to experiments is discussed, and we suggest that the direction of the temperature dependence may be controlled not only by the solution behaviour of the solvophobic block (upper critical solution temperature-like versus lower critical solution temperature-like) but also by chi_{AB}. 

History

School affiliated with

  • School of Mathematics and Physics (Research Outputs)

Publication Title

Soft Matter

Volume

17

Issue

20

Pages/Article Number

3628-3634

Publisher

Royal Society of Chemistry

ISSN

1744-683X

eISSN

1744-6848

Date Submitted

2024-03-20

Date Accepted

2024-04-08

Date of First Publication

2024-04-09

Date of Final Publication

2024-05-07

Open Access Status

  • Open Access

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