Holder, Simon J., McKenzie, Beulah E., de Visser, Joël F., Friedrich, Heiner, Wirix, Maarten J. M., Bomans, Paul H. H., de With, Gijsbertus, Sommerdijk, Nico A. J. M. (2013) Bicontinuous Nanospheres from Simple Amorphous Amphiphilic Diblock Copolymers. Macromolecules, 46 (24). pp. 9845-9848. ISSN 0024-9297. (doi:10.1021/ma4019729) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:65091)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: https://doi.org/10.1021/ma4019729 |
Abstract
Bicontinuous nanospheres have been observed (although rarely) from a variety of block copolymers with architectural and compositional complexity, and often in the presence of additives. Unlocking key features involved in their formation presents possibilities for bicontinuous aggregates with varied functionality and application. An attractive prospect is the ability to form them from much simpler polymeric structures derived from facile syntheses. To that end, we herein report the formation of bicontinuous aggregates from simple amorphous amphiphilic diblock copolymers of poly(ethylene oxide)-b-poly(n-butyl methacrylate), analogous to our previous report of the same from a semicrystalline comb-like block copolymer. Moreover, we demonstrate that polymorphism can be achieved by altering the relative block proportions and the nonselective cosolvent. We find that the polymeric structure is not the dominating factor in the formation of bicontinuous nanospheres but that the choice of cosolvent for the hydrophilic block appears to have greater influence on determining the end morphology
Item Type: | Article |
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DOI/Identification number: | 10.1021/ma4019729 |
Divisions: | Divisions > Division of Natural Sciences > Physics and Astronomy |
Depositing User: | Simon Holder |
Date Deposited: | 07 Dec 2017 14:31 UTC |
Last Modified: | 05 Nov 2024 11:02 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/65091 (The current URI for this page, for reference purposes) |
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