High molecular weight bio furan-based co-polyesters for food packaging applications: synthesis, characterization and solid-state polymerization

2016 ◽  
Vol 18 (19) ◽  
pp. 5142-5150 ◽  
Author(s):  
Sungmin Hong ◽  
Kyung-Deok Min ◽  
Byeong-Uk Nam ◽  
O Ok Park

High molecular weight bio furan-based copolyesters have been synthesized by melt polycondensation and solid-state polymerization for packaging applications as bio based alternatives to PET.

e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Kim Seok Hoon ◽  
Kim Joon Ho

AbstractSolid-state polymerization has been widely used to prepare high molecular weight poly(ethylene terephthalate). Solid-state polymerization is generally carried out by heating solid, melt-phase-polymerized polymer below its melting temperature but above its glass transition temperature. Solid-state polymerization of poly(trimethylene terephthalate)(PTT) is not an independent process but rather an additional process with respect to melt polymerization that is used when PTT of a higher molecular weight is required. Two kinds of commercial PTT chips were polymerized in the solid state to prepare high molecular weight PTT, which were characterized by end group contents, molecular weight, thermal analysis and X-ray diffraction. In the solid-state polymerization of PTT, the overall reaction rate was governed by the reaction temperature, reaction time and pellet size. The content of carboxyl end groups was decreased during the solid-state polymerization with increasing reaction time and temperature. The melting temperature and crystallinity of solid-state-polymerized PTT were higher at longer times and higher temperatures of polymerization. The activation energy for the solid-state polymerization of PTT was in the range of 24~25 kcal/mol for each chip. Through the solid-state polymerization of commercial PTT chips, we could get high molecular weight polymers up to an intrinsic viscosity value of 1.63 dl/g, which is equivalent to about a 117,000 weight-average molecular weight.


1993 ◽  
Vol 26 (5) ◽  
pp. 1186-1187 ◽  
Author(s):  
V. S. Iyer ◽  
J. C. Sehra ◽  
K. Ravindranath ◽  
S. Sivaram

2001 ◽  
Vol 34 (12) ◽  
pp. 3916-3920 ◽  
Author(s):  
Stephen M. Gross ◽  
George W. Roberts ◽  
Douglas J. Kiserow ◽  
Joseph M. DeSimone

Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4880
Author(s):  
Lazaros Papadopoulos ◽  
Eleftheria Xanthopoulou ◽  
George N. Nikolaidis ◽  
Alexandra Zamboulis ◽  
Dimitris S. Achilias ◽  
...  

In the era of polymers from renewable resources, polyesters derived from 2,5 furan dicarboxylic acid (FDCA) have received increasing attention due to their outstanding features. To commercialize them, it is necessary to synthesize high molecular weight polymers through efficient and simple methods. In this study, two furan-based polyesters, namely poly (propylene furanoate) (PPF) and poly(butylene furanoate) (PBF), were synthesized with the conventional two-step melt polycondensation, followed by solid-state polycondensation (SSP) conducted at different temperatures and reaction times. Molecular weight, structure and thermal properties were measured for all resultant polyesters. As expected, increasing SSP time and temperature results in polymers with increased intrinsic viscosity (IV), increased molecular weight and reduced carboxyl end-group content. Finally, those results were used to generate a simple mathematical model that prognosticates the time evolution of the materials’ IV and end groups concentration during SSP.


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