Abstract

The effects of the length of each hydrophobic end block N_{st} and polymer concentration \bar{\phi}_{P} on the transition broadness in amphiphilic ABA symmetric triblock copolymer solutions are studied using the self-consistent field lattice model. When the system is cooled, micelles are observed, i.e.,the homogenous solution (unimer)-micelle transition occurs. When N_{st} is increased, at fixed \bar{\phi}_{P}, micelles occur at higher temperature, and the temperature-dependent range of micellar aggregation and half-width of specific heat peak for unimer-micelle transition increase monotonously. Compared with associative polymers, it is found that the magnitude of the transition broadness is determined by the ratio of hydrophobic to hydrophilic blocks, instead of chain length. When \bar{\phi}_{P} is decreased, given a large N_{st}, the temperature-dependent range of micellar aggregation and half-width of specific heat peak initially decease, and then remain nearly constant. It is shown that the transition broadness is concerned with the changes of the relative magnitudes of the eductions of nonstickers and solvents from micellar cores.

Highlights

  • Amphiphilic block copolymers are versatile macromolecules because they allow for a rich variety of different structures

  • It is found that the magnitude of the transition broadness is related to the relative changes of the eductions of nonsticker and solvent from micellar cores

  • The amphiphilic ABA symmetric triblock copolymers depend on three tunable molecular parameters: χ, Nns and Nst

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Summary

Introduction

Amphiphilic block copolymers are versatile macromolecules because they allow for a rich variety of different structures Their length and the number of blocks of each species can be tuned at will, from di- and triblock to multiblock copolymers. The transition region most copolymer molecules are in micelles It is verified theoretically [5] and experimentally [6] that the broad nature should be ascribed to the structural changes which accompany the replacement of micellar core solvent by polymer. The study of the effects of polymer concentration and length of hydrophobic end block on the transition broadness in amphiphilic ABA symmetric triblock copolymer solutions would be quite useful to understand the thermodynamics of block copolymers in a selective solvent. Amphiphilic ABA symmetric triblock copolymer solutions are studied using SCFT lattice model. It is found that the magnitude of the transition broadness is related to the relative changes of the eductions of nonsticker and solvent from micellar cores

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