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  5. Advanced mechanical properties of amphiphilic polymer conetworks through hierarchical reinforcement with peptides and cellulose nanocrystals
 
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2025
Zweitveröffentlichung
Artikel
Verlagsversion

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

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Hauptpublikation
D4PY01283F.pdf
CC BY 3.0 Unported
Format: Adobe PDF
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TUDa URI
tuda/13816
URN
urn:nbn:de:tuda-tuprints-300981
DOI
10.26083/tuprints-00030098
Autor:innen
Velasquez, Sara T. R. ORCID 0000-0002-9943-9050
Jang, Daseul ORCID 0000-0003-0138-4627
Thomas, Jessica ORCID 0000-0002-8648-2455
Grysan, Patrick ORCID 0000-0003-2081-8267
Korley, LaShanda T. J. ORCID 0000-0002-8266-5000
Bruns, Nico ORCID 0000-0001-6199-9995
Kurzbeschreibung (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-hydroxyethyl 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.

Sprache
Englisch
Fachbereich/-gebiet
07 Fachbereich Chemie > Ernst-Berl-Institut > Fachgebiet Makromolekulare Chemie
Forschungs- und xchange Profil
Interdisziplinäre Forschungsprojekte > Centre for Synthetic Biology
DDC
500 Naturwissenschaften und Mathematik > 540 Chemie
500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
Institution
Universitäts- und Landesbibliothek Darmstadt
Ort
Darmstadt
Titel der Zeitschrift / Schriftenreihe
Polymer Chemistry
Startseite
2618
Endseite
2628
Jahrgang der Zeitschrift
16
Heftnummer der Zeitschrift
22
ISSN
1759-9962
Verlag
Royal Society of Chemistry
Ort der Erstveröffentlichung
Cambridge
Publikationsjahr der Erstveröffentlichung
2025
Verlags-DOI
10.1039/D4PY01283F
PPN
534362753
Ergänzende Ressourcen (Forschungsdaten)
https://doi.org/10.15129/7fc1b9a7-99d2-4666-8709-e0d319afd131

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