4.7 Article

Structure-property insights of semi-aromatic polyamides based on renewable furanic monomer and aliphatic diamines

Journal

EUROPEAN POLYMER JOURNAL
Volume 178, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2022.111496

Keywords

Polyamides; Bio-based; 5-Furandicarboxylic acid (FDCA); Polycondensation

Funding

  1. European Union [665992]
  2. Corbion Biochem B.V
  3. EPSRC [EP/R027129/1]
  4. Marie Curie Actions (MSCA) [665992] Funding Source: Marie Curie Actions (MSCA)

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A series of semi-aromatic polyamides based on a renewable monomer FDCA were synthesized using an environmentally friendly melt polycondensation technique. The newly synthesized furan-based polyamides showed high molecular weights, high glass transition temperatures, and comparable thermal stabilities to petroleum-based counterparts. Various analytical techniques were used to study the structure and properties of these polyamides.
A series of semi-aromatic polyamides based on a renewable monomer, 2,5-furandicarboxylic acid (FDCA) has been reported. The dimethyl ester derivative of FDCA (DMFDC) was subjected to polymerization with aliphatic diamines differing in carbon chain length, through an environmentally benign melt polycondensation technique using titanium(IV) isopropoxide (TIPT) catalyst at low concentrations (400 ppm). The newly synthesized furan-based polyamides (FPAs) showed molecular weights in the range of Mn = 8-11 kg/mol and Mw = 29-32 kg/mol and high glass transition temperatures (Tg range 97-140 C). The structure and properties of these FPAs were investigated using various analytical techniques. DSC analysis showed absence of crystallization and melting behaviour, indicating predominantly an amorphous character of these FPAs, which was further confirmed by DMA analysis. However, Poly(butylene furanamide) (PA4F) showed presence of crystalline regions exhibited in the form of several peaks on the WAXD pattern. These peaks were attributed to the isothermal crystallization caused by the annealing effects during synthesis. The FPAs also showed comparable thermal stabilities to their petroleum-based counterparts as measured by the TGA and found to be thermally stable up to 400 C. Poly (decamethylene furanamide) (PA10F) displayed the highest thermal stability (Td -max = 446 C). MALDI-ToF MS revealed various end-groups in addition to the expected amino and ester end-groups arising from the side re-actions, such as, pyrrolidine (PA4F), N-methylation, decarboxylation and triamine formation. Presence of these end was ascribed to the for the

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