Premium
Ordered Nanostructures of Carbon Nanotube–Polymer Composites from Lyotropic Liquid Crystal Templating
Author(s) -
Kasprzak Christopher R.,
Scherzinger Evan T.,
Sarkar Amrita,
Miao Miranda,
Porcincula Dominique H.,
Madriz Alejandro M.,
Pennewell Zachary M.,
Chau Sophia S.,
Fernando Raymond,
Stefik Morgan,
Zhang Shanju
Publication year - 2018
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201800197
Subject(s) - materials science , lyotropic , polymerization , alkyl , carbon nanotube , polymer , chemical engineering , hexagonal phase , lyotropic liquid crystal , nanocomposite , lamellar structure , liquid crystal , polymer chemistry , phase (matter) , composite material , organic chemistry , chemistry , liquid crystalline , optoelectronics , engineering
A series of polymer nanocomposites containing single‐walled carbon nanotubes (SWNTs) are prepared from polymerizable quaternary ammonium surfactants using photo‐polymerization and investigated by means of polarized optical microscopy, small‐angle X‐ray scattering, and rheological measurements. The surfactant monomers with various alkyl chains of nonpolar tails form lyotropic liquid crystalline (LLC) mesophases in aqueous medium with hexagonal packing of cylindrical micelles. The physical adsorption of nonpolar tails of surfactants on the surface of SWNTs results in de‐bundled nanotubes. The LLC phase diagram is investigated as functions of alkyl chain length, concentration, temperature, and SWNTs. As such, addition of SWNTs does not change the hexagonal mesophases but enhances the order–disorder transition temperatures and alters the rheological behaviors. After photo‐polymerization, the microstructures of hexagonal packing are changed while addition of SWNTs does not disrupt the resulting microstructures. The polymerized composites are consistent with both lamellar and gyroid nanostructures and a possible model is proposed to interpret the observed phenomenon. Under the shear flow, the defect‐free monodomain structures are obtained in the LLC phase and subsequently locked in the solid film after polymerization.