Advanced mechanical properties of amphiphilic polymer conetworks through hierarchical reinforcement with peptides and cellulose nanocrystals

Sara T. R. Velasquez, Daseul Jang, Jessica Thomas, Patrick Grysan, LaShanda T. J. Korley, Nico Bruns*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Amphiphilic polymer conetworks (APCNs) have been explored for various applications, including soft contact lenses, biomaterials, and membranes. They combine important properties of hydrogels and elastomers, including elasticity, transparency, and the capability to swell in water. Moreover, they also swell in organic solvents. However, their mechanical properties could be improved. We developed a two-level, bio-inspired, hierarchical reinforcement of APCNs using cellulose nanocrystals (CNCs) to reinforce peptide-reinforced APCNs formed from hydrophobic poly-β-benzyl-L-aspartate-block-polydimethylsiloxane-block-poly-β-benzyl-L-aspartate (PBLA-b-PDMS-b-PBLA) triblock copolymer crosslinkers and hydrophilic poly(2-hydroxy ethyl acrylate) (PHEA) chain segments. Bio-inspired peptide-polymer hybrids combine the structural hierarchy often found in natural materials with synthetic macromolecules, such as block copolymers with soft and hard segments, to enhance their mechanical properties. On the other hand, CNCs provide an additional means to dissipate mechanical energy in polymeric materials, thereby enhancing reinforcement. The key to homogeneously incorporating CNCs into the APCNs is the combination of hydrophobic CNCs (HCNCs) with peptide-blocks in the APCNs, exploiting the hydrogen bonding capability of the peptides to disperse the HCNCs. The effect of HCNCs on the ability of APCNs to swell in water and organic solvents, as well as on their thermal and mechanical properties, was characterized. Additionally, the nanostructure of the materials was analyzed via small-angle X-ray scattering (SAXS) and wide-angle X-ray scattering (WAXS). The swellability of the HCNC-containing APCNs was independent of the HCNC concentration, and all samples were highly transparent. The ideal HCNC concentration, in terms of maximal stress, strain, toughness, and reinforcement, was found to be between 6 and 15 wt%. An increase in Young´s modulus of up to 500% and toughness of up to 200% was achieved. The hierarchical reinforcement also greatly strengthened the APCNs when swollen in water or n-hexane. Thus, HCNCs and peptide segments can be used to reinforce APCNs and to tailor their properties.
Original languageEnglish
Pages (from-to)2618-2628
Number of pages11
JournalPolymer Chemistry
Volume16
Issue number22
Early online date25 Apr 2025
DOIs
Publication statusPublished - 14 Jun 2025

Funding

The project received funding from the Partnership for International Research and Education (PIRE) Bio-inspired Materials and Systems, supported by the U.S. National Science Foundation under Grant No. OISE 1844463 and the Swiss National Science Foundation under Grant No. 177995. Moreover, this work benefitted from support from the Swiss National Science Foundation through the National Center of Competence in Research (NCCR) Bio-Inspired Materials (Grant No. 51NF40-182881). The work carried out at LIST was part of the ACP 22 project framework.

Keywords

  • bio-inspiration
  • amphiphilic polymer conetworks
  • hydrogels
  • peptides
  • mechanical properties
  • cellulose nanocrystals
  • composites

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