Bio-based degradable poly(ether-ester)s from melt-polymerization of aromatic ester and ether diols

Abstract: 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 (Mw = 5.3–7.9 × 104 g.mol−1) and polydispersity index (Đ) values of 1.54–2.88. Thermal analysis showed the polymers are semi-crystalline materials with melting temperatures of 204–240 °C, and tunable glass transition temperatures (Tg) of 98–120 °C. Their 5% decomposition temperature (Td,5%) varied from 430–315 °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

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
International journal of molecular sciences. - 23, 16 (2022) , 8967, ISSN: 1422-0067

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2022
Creator
Djouonkep, Lesly Dasilva Wandji
Tchameni, Alain Pierre
Selabi, Naomie Beolle Songwe
Kamdem Tamo, Arnaud
Dönch, Ingo
Cheng, Zhengzai
Gauthier, Mario
Xie, Binqiang
Osorio-Madrazo, Anayancy

DOI
10.3390/ijms23168967
URN
urn:nbn:de:bsz:25-freidok-2290184
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:52 PM CET

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Associated

Time of origin

  • 2022

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