4.7 Article

Bio-Based Degradable Poly(ether-ester)s from Melt-Polymerization of Aromatic Ester and Ether Diols

Journal

Publisher

MDPI
DOI: 10.3390/ijms23168967

Keywords

bio-based poly(ether-ester)s; mechanical properties; gas barrier properties; (bio)degradation

Funding

  1. Baden-Wuerttemberg Ministry of Science, Research, the Arts (MWK)
  2. University of Freiburg
  3. National Natural Science Foundation of China [51974034, 51404040, 52150410427]
  4. Emmy Noether Programme of the German Research Foundation DFG [OS 497/6-1]

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Vanillin, a promising aromatic aldehyde, can be used in the design of novel sustainable polymeric materials. A series of poly(ether-ester)s were synthesized using vanillin-derived monomers, showing high molecular weights, semi-crystallinity, excellent thermal and mechanical properties, and good biodegradability.
Vanillin, as a promising aromatic aldehyde, possesses worthy structural and bioactive properties useful in the design of novel sustainable polymeric materials. Its versatility and structural similarity to terephthalic acid (TPA) can lead to materials with properties similar to conventional poly(ethylene terephthalate) (PET). In this perspective, a symmetrical dimethylated dialkoxydivanillic diester monomer (DEMV) derived from vanillin was synthesized via a direct-coupling method. Then, a series of poly(ether-ester)s were synthesized via melt-polymerization incorporating mixtures of phenyl/phenyloxy diols (with hydroxyl side-chains in the 1,2-, 1,3- and 1,4-positions) and a cyclic diol, 1,4-cyclohexanedimethanol (CHDM). The polymers obtained had high molecular weights (M-w = 5.3-7.9 x 10(4) g.mol(-1)) and polydispersity index (D) values of 1.54-2.88. Thermal analysis showed the polymers are semi-crystalline materials with melting temperatures of 204-240 degrees C, and tunable glass transition temperatures (T-g) of 98-120 degrees C. Their 5% decomposition temperature (T-d,T-5%) varied from 430-315 degrees C, which endows the polymers with a broad processing window, owing to their rigid phenyl rings and trans-CHDM groups. These poly(ether-ester)s displayed remarkable impact strength and satisfactory gas barrier properties, due to the insertion of the cyclic alkyl chain moieties. Ultimately, the synergistic influence of the ester and ether bonds provided better control over the behavior and mechanism of in vitro degradation under passive and enzymatic incubation for 90 days. Regarding the morphology, scanning electron microscopy (SEM) imaging confirmed considerable surface degradation in the polymer matrices of both polymer series, with weight losses reaching up to 35% in enzymatic degradation, which demonstrates the significant influence of ether bonds for biodegradation.

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