Role of Poly(ethylene glycol) Di(meth)acrylate Cross-linkers in Modulating Structures of Hexagonal Lyotropic Liquid Crystal toward Enhanced Nanofiltration

Hexagonal lyotropic liquid crystals (HLLCs) have become a very attractive nanostructured template for fabricating nanofiltration active layers. While introducing cross-linkers into HLLC stabilizes their structure via covalent networks, it often compromises interfacial stability. We investigated this trade-off using solid-state NMR and small-angle X-ray scattering. We found that a poly(ethylene glycol) di(meth)acrylate (PEGDA) cross-linker with a medium chain length (nine units) and a bulky end group optimally stabilizes the HLLC interface. The medium chain ensures targeted localization within hydrophilic domains, while the bulky group provides steric hindrance, minimizing disruptive interactions with surfactants. This structural synergy enables significantly higher cross-linker loading without inducing phase transitions. Consequently, the heavily cross-linked system maintains well-ordered hexagonal mesophases with continuous, defect-free water pathways. This structural integrity translates to a dramatic enhancement in the permeability of the HLLC-templated active layer, increasing from 1.6 to 7 L m –2 h –1 bar –1 μm.

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Publication Details

Journal
Macromolecules
Published
2026-06-26
DOI
https://doi.org/10.1021/acs.macromol.6c00788
Primary Topic
Liquid Crystal Research Advancements
Type
article
Field-Weighted Citation Impact
0.00

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article

Role of Poly(ethylene glycol) Di(meth)acrylate Cross-linkers in Modulating Structures of Hexagonal Lyotropic Liquid Crystal toward Enhanced Nanofiltration

Liliana de Campo, Nathan E. Stott, Luke A. O’Dell, Zhao Zhang et al.
Macromolecules
Liquid Crystal Research Advancements
article

Role of Poly(ethylene glycol) Di(meth)acrylate Cross-linkers in Modulating Structures of Hexagonal Lyotropic Liquid Crystal toward Enhanced Nanofiltration

Liliana de Campo, Nathan E. Stott, Luke A. O’Dell, Zhao Zhang, Lingxue Kong, Senlin Gu, Yuxi Xu, Imran Shakir, Tianhao Ge, Liangliang Zhang, Guang Wang
article en

Abstract

Hexagonal lyotropic liquid crystals (HLLCs) have become a very attractive nanostructured template for fabricating nanofiltration active layers. While introducing cross-linkers into HLLC stabilizes their structure via covalent networks, it often compromises interfacial stability. We investigated this trade-off using solid-state NMR and small-angle X-ray scattering. We found that a poly(ethylene glycol) di(meth)acrylate (PEGDA) cross-linker with a medium chain length (nine units) and a bulky end group optimally stabilizes the HLLC interface. The medium chain ensures targeted localization within hydrophilic domains, while the bulky group provides steric hindrance, minimizing disruptive interactions with surfactants. This structural synergy enables significantly higher cross-linker loading without inducing phase transitions. Consequently, the heavily cross-linked system maintains well-ordered hexagonal mesophases with continuous, defect-free water pathways. This structural integrity translates to a dramatic enhancement in the permeability of the HLLC-templated active layer, increasing from 1.6 to 7 L m –2 h –1 bar –1 μm.

Macromolecules
Australian Nuclear Science and Technology Organisation (AU), Deakin University (AU), Chinese Academy of Sciences (CN), Westlake University (CN), China Spallation Neutron Source (CN), Institute for Advanced Study (DE), Islamic University of Madinah (SA), University of Chinese Academy of Sciences (CN), Spallation Neutron Source
Australian Institute of Nuclear Science and Engineering, Deakin University, National Natural Science Foundation of China, Australian Research Council
Clean water and sanitation
Openalex Percentile: Top 17%
Liquid Crystal Research Advancements
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