Towards sugar-derived polyamides as environmentally friendly materials

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

DOI

  • Aleksandra Wroblewska, Gdansk Univ Technol, Gdansk University of Technology, Fac Chem, Dept Polymer Technol
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  • Arkadiusz Zych, Gdansk Univ Technol, Gdansk University of Technology, Fac Chem, Dept Polymer Technol
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  • Shanmugam Thiyagarajan, Wageningen Univ & Res Ctr, Wageningen University & Research Center, Food & Biobased Res
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  • Dmytro Dudenko, Max Planck Inst Polymer Res, Max Planck Society
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  • Daan van Es, Wageningen Univ & Res Ctr, Wageningen University & Research Center, Food & Biobased Res
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  • Michael Ryan Hansen, Max Planck Institute for Polymer Research
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  • Cor Koning, Eindhoven Univ Technol, Eindhoven University of Technology, Lab Polymer Technol, Dept Chem Engn & Chem
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  • Rob Duchateau, Eindhoven Univ Technol, Eindhoven University of Technology, Lab Polymer Technol, Dept Chem Engn & Chem
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  • Lidia Jasinska-Walc, Eindhoven Univ Technol, Eindhoven University of Technology, Lab Polymer Technol, Dept Chem Engn & Chem

As part of our ongoing study investigating isohexide-based polyamides, we have synthesized isosorbide (bis(propan-1-amine)) (DAPIS) and studied its reactivity in the polymerization towards fully biobased polyamides. Polycondensation of nylon salts with various contributions of DAPIS afforded a family of homo-and copolyamides, which were characterized using complementary spectroscopic techniques. The chemical structure of the materials was determined by FT-IR, 1D and 2D liquid-state NMR spectroscopy, whilst the supramolecular arrangement, conformational changes upon heating, and molecular mobility of the polymers were investigated by solid-state C-13{H-1} Cross-Polarization/Magic-Angle Spinning (CP/MAS) NMR and C-13{H-1} Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) experiments. The abundance of the different DAPIS conformers was determined by DFT-D computational methods. The thermal properties of the polyamides were tested for polymers with different amounts of isohexide units in the backbone by DSC and TGA, demonstrating that the increasing amounts of isohexide diamines efficiently decrease their melting points and slightly decrease their thermal stability. The relaxation processes of the isohexide-derived polyamides were studied by DMTA.

Original languageEnglish
JournalPolymer Chemistry
Volume6
Issue22
Pages (from-to)4133-4143
Number of pages11
ISSN1759-9954
DOIs
Publication statusPublished - 2015

    Research areas

  • SOLID-STATE NMR, DICARBOXYLIC-ACID UNITS, CHIRAL BUILDING-BLOCKS, D-MANNITOL, POLARIZATION TRANSFER, RENEWABLE RESOURCES, POLY(BUTYLENE TEREPHTHALATE), BICYCLIC DIOL, D-GLUCITOL, POLYESTERS

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