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Role of enhanced solubility in esterification of 2,5-furandicarboxylic acid with ethylene glycol at reduced temperatures: energy efficient synthesis of poly(ethylene 2,5-furandicarboxylate)
- Source :
- Reaction Chemistry & Engineering. 3:447-453
- Publication Year :
- 2018
- Publisher :
- Royal Society of Chemistry (RSC), 2018.
-
Abstract
- Poly(ethylene 2,5-furandicarboxylate) (PEF) has garnered considerable industrial and academic interest as a renewable alternative to traditional polyesters due to its superior barrier and thermal properties. While efforts for the industrial scale production of PEF from 2,5-furandicarboxylic acid (FDCA) and ethylene glycol (EG) are underway, most of the published literature on PEF follows the conventional terephthalic acid (TPA) based polyester synthesis protocol. In this study, we reveal for the first time that the solubility of FDCA is an order of magnitude higher in EG compared to that in TPA at the process temperatures. The enhanced solubility of FDCA in EG results in improved esterification kinetics especially at temperatures from 180–210 °C to yield complete end group conversion. We further demonstrate that it is advantageous to perform the direct esterification step of PEF synthesis in a lower temperature range than that in previous reports reducing the potential side reactions in addition to cost and energy savings at the industrial scale. This work can provide new insights into the sustainable synthesis of FDCA-based polyesters for bio-based packaging.
- Subjects :
- Fluid Flow and Transfer Processes
Terephthalic acid
Ethylene
Chemistry
Process Chemistry and Technology
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Catalysis
0104 chemical sciences
Polyester
chemistry.chemical_compound
End-group
Chemical engineering
Chemistry (miscellaneous)
Yield (chemistry)
Chemical Engineering (miscellaneous)
2,5-Furandicarboxylic acid
Solubility
0210 nano-technology
Ethylene glycol
Subjects
Details
- ISSN :
- 20589883
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- Reaction Chemistry & Engineering
- Accession number :
- edsair.doi...........eb7dda0d63670b9ae179cd5e5c81c1ec
- Full Text :
- https://doi.org/10.1039/c8re00086g