Two Robust Strategies toward Hydrogels from Quenched Block Copolymer Nanofibrillar Micelles
Author(s) -
Kai Zhang,
Aaditya Suratkar,
Sitara Vedaraman,
Vasudevan Lakshminarayanan,
Laurence Jennings,
Piotr J. Glazer,
Jan H. van Esch,
Eduardo Mendes
Publication year - 2018
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.8b01158
Subject(s) - micelle , copolymer , self healing hydrogels , rheology , chemical engineering , materials science , ethylene oxide , polystyrene , transmission electron microscopy , fusion , polymer chemistry , chemistry , polymer , nanotechnology , organic chemistry , aqueous solution , composite material , linguistics , philosophy , engineering
While the formation of (tri)block copolymer hydrogels has been extensively investigated, such studies mostly focused on equilibrium self-assembling whereas the use of preformed structures as building blocks such as out of equilibrium, quenched, nanofibrillar micelles is still a challenge. Here, we demonstrate that quenched, ultralong polystyrene- b -poly(ethylene oxide) (PS- b -PEO) micelles can be used as robust precursors of hydrogels. Two cross-linking strategies, (i) thermal fusion of micellar cores and (ii) chemical cross-linking of preformed micellar coronas were studied. The gelation process and the structure of the micellar networks were investigated by in situ rheological measurements, confocal microscopy and transmission electron microscopy. Direct observation of core fusion of preformed quenched micelles is provided validating this method as a robust gelation route. Using time sweep rheological experiments, it was found for both cross-linking methods that these 3D "mikado" gels are formed in three different stages, containing (1) initiation, (2) transition (growth), and (3) stabilization regimes.
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