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Updated: Oct 19, 2025

Facile Preparation of Internally Self-assembled Lipid Particles Stabilized by Carbon Nanotubes
Published on: February 19, 2016
Controlling phase and rheological behaviours of hexagonal lyotropic liquid crystalline templates for nanostructural
Guang Wang1, Christopher J Garvey2, Senlin Gu3
1Institute of High Energy Physics, Chinese Academy of Sciences, 100049, Beijing, China; Spallation Neutron Source Science Centre, 523803, Dongguan, China; Deakin University, Geelong, Institute for Frontier Materials, Locked Bag 20000, VIC 3220, Australia; Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovského nám.2, 162062, Prague 6, The Czech Republic.
Abstract:
Introducing polymerizable monomers into a binary hexagonal lyotropic liquid crystalline (LLC) template is a straightforward way for retaining the nanostructure but will decrease attractive intra- and inter- aggregate interactions. It is therefore crucial to understand the interfacial interactions at nanoscale after introducing the monomers but prior to polymerization. Herein, active species, poly (ethylene glycol) diacrylate (PEGDA) and 2-hydroxyethyl methacrylate (HEMA), were introduced into hexagonal LLC of dodecyl trimethylammonium bromide and water to explore the structural variables, dimensional stability, and dynamic property. At a proper volume ratio of PEGDA/HEMA (1/4), the system presents excellent homogeneity with a higher dimensional stability and lower dynamic property from rheological assessments, thereby achieving robust, free-standing, and transparent membranes after photo-polymerization. The unique property of the system also lies in the much lower order-disorder transition temperature (45 °C) that facilitates the reorientation of mesochannels. They are in contrast inaccessible for the ternary system only with PEGDA, though the nanostructure for both systems could be retained. An insight into subtle variations in these parameters allows us to prepare a polymerizable template possessing higher dimensional stability and suitable flexibility via molecular design, thereby enabling simultaneous structural alignment and retention for the development of functional nanomaterials.

