Issue 9, 2015

Semi-crystalline polymethylene-b-poly(acrylic acid) diblock copolymers: aggregation behavior, confined crystallization and controlled growth of semicrystalline micelles from dilute DMF solution

Abstract

In this paper, we have systematically investigated the aggregation behavior, confined crystallization and controlled growth of a novel polyolefin analogue-containing block copolymers (BCPs), i.e., polymethylene-b-poly(acrylic acid) diblock copolymers (PM-b-PAA). On cooling from a homogenous DMF solution at 80 °C, PM-b-PAA was found to crystallize and aggregate with well-defined disk-like micelles. The aggregate behavior and in-plane morphology of PM-b-PAA could be easily controlled by modifying the block ratio, solution pH and solvent composition (DMF–water), by manipulating the crystallization of PM block and the stretching degree of solvated PAA corona. Further investigation of the crystalline feature of PM-b-PAA indicated that the crystallization of PM was retarded by tethered amorphous PAA segments. The crystalline micelle could construct a nano-confined environment with PM folding as the core into a thickness of the mono-layered polyethylene. Finally, when cultured in dilute DMF solution at 50 °C, the initial crystalline micelles, being as self-seeds, could follow a living growth mechanism and develop into single crystals, with well-defined lozenge-shaped morphology.

Graphical abstract: Semi-crystalline polymethylene-b-poly(acrylic acid) diblock copolymers: aggregation behavior, confined crystallization and controlled growth of semicrystalline micelles from dilute DMF solution

Supplementary files

Article information

Article type
Paper
Submitted
22 Nov 2014
Accepted
04 Jan 2015
First published
06 Jan 2015

Soft Matter, 2015,11, 1778-1787

Author version available

Semi-crystalline polymethylene-b-poly(acrylic acid) diblock copolymers: aggregation behavior, confined crystallization and controlled growth of semicrystalline micelles from dilute DMF solution

H. Wang, C. Wu, G. Xia, Z. Ma, G. Mo and R. Song, Soft Matter, 2015, 11, 1778 DOI: 10.1039/C4SM02581D

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