Structural, thermal and rheological studies on newly developed polyesters randomly copolymerized with poly (tetramethylene glycol) (PTMG)

2008 ◽  
Vol 1151 ◽  
Author(s):  
Matsumoto Osamu ◽  
Hotta Atsushi

ABSTRACTPoly (cyclohexanedimethanol cyclohexanedicarboxlic acid) (PCC), a fairly newly synthesized polyester, has been studied. Having a good experience of increasing both thermal stability and service temperature when applied to typical polymers, poly (tetramethylene glycol) (PTMG) was selected as a softening agent that was randomly copolymerized into the PCC chains. Another widely-used polyester, poly (ethylene terephthalate) (PET) was also produced in order to investigate the effect of PTMG, which was compared with the properties of the newly developed random PCC-PTMG copolymers (PCCP). In this study, the crystalline structures, the thermal and the mechanical properties of both PCC and PET containing different ratios of the random segment of PTMG were investigated by differential scanning calorimetery (DSC) and tensile tester.It was found that the crystallization rate of pure PCC was significantly slow, whereas for PCCP, PTMG effectively accelerated the crystallization rate with increasing PTMG, and the sample with 25 wt% of PTMG had the fastest crystallization rate in all PCCP samples. Here, the PTMG acted as an accelerator, simultaneously depressing the movement of PCC molecular chains. The elastic recovery test indicated that the ability of PTMG as a softening agent was highly demonstrated at 20 wt% of PTMG. The results of PCCP were compared with those of PET-PTMG copolymers (PETP) and it was found that there were optimum values of PTMG for the crystallization rate on both samples. Additionally, the results of the elastic recovery test indicated that the softening effects observed in PCCP were more pronounced than those observed in PETP.

RSC Advances ◽  
2017 ◽  
Vol 7 (59) ◽  
pp. 37139-37147 ◽  
Author(s):  
Diran Wang ◽  
Faliang Luo ◽  
Zhiyuan Shen ◽  
Xuejian Wu ◽  
Yaping Qi

In order to overcome low crystallization rate of PET, HPN-68L was selected to replace the special nucleate agent of PET to improve PET crystallization for its carboxylate anion structure which usually showed high induced nucleation ability for PET.


Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3053
Author(s):  
Shichang Chen ◽  
Shangdong Xie ◽  
Shanshan Guang ◽  
Jianna Bao ◽  
Xianming Zhang ◽  
...  

Three kinds of modified poly(ethylene terephthalate) (PET) were prepared by solution blending combined with melt post-polycondensation, using 4,4′-thiodiphenol (TDP), 4,4′-oxydiphenol (ODP) and hydroquinone (HQ) as the bisphenols, respectively. The effects of TDP, ODP and HQ on melt post-polycondensation process and crystallization kinetics, melting behaviors, crystallinity and thermal stability of PET/bisphenols complexes were investigated in detail. Excellent chain growth of PET could be achieved by addition of 1 wt% bisphenols, but intrinsic viscosity of modified PET decreased with further bisphenols content. Intermolecular hydrogen bonding between carbonyl groups of PET and hydroxyl groups of bisphenols were verified by Fourier transform infrared spectroscopy. Compare to pure PET, both the crystallization rate and melting temperatures of PET/bisphenols complexes were reduced obviously, suggesting an impeded crystallization and reduced lamellar thickness. Moreover, the structural difference between TDP, ODP and HQ played an important role on crystallization kinetics. It was proposed that the crystallization rate of TDP modified PET was reduced significantly due to the larger amount of rigid benzene ring and larger polarity than that of PET with ODP or HQ. X-ray diffraction results showed that the crystalline structure of PET did not change from the incorporation of bisphenols, but crystallinity of PET decreased with increasing bisphenols content. Thermal stability of modified PET declined slightly, which was hardly affected by the molecular structure of bisphenols.


2019 ◽  
Vol 253 ◽  
pp. 02005
Author(s):  
Daniel Gere ◽  
Tibor Czigany

Nowadays, PLA is increasingly used as a packaging material, therefore it may appear in the petrol-based polymer waste stream. However, with the today’s mechanical recycling technologies PLA and PET bottles cannot be easily or cheaply separated. Therefore, our goal was to investigate the mechanical, morphological and thermal properties of different PET and PLA compounds in a wide range of compositions. We made different compounds from poly(ethylene-terephthalate) (PET) and poly(lactic acid) (PLA) by extrusion, and injection molded specimens from the compounds. We investigated the mechanical properties and the phase morphology of the samples and the thermal stability of the regranulates. PET and PLA are thermodynamically immiscible, therefore we observed a typical island-sea type morphology in SEM micrographs. When PLA was added, the mechanical properties (tensile strength, modulus, elongation at break and impact strength) changed significantly. The Young’s modulus increased, while elongation at break and impact strength decreased with the increase of the weight fraction of PLA. The TGA results indicated that the incorporation of PLA decreased the thermal stability of the PET/PLA blends.


2008 ◽  
Vol 109 (6) ◽  
pp. 4112-4120 ◽  
Author(s):  
Xuepei Yuan ◽  
Chuncheng Li ◽  
Guohu Guan ◽  
Yaonan Xiao ◽  
Dong Zhang

Sign in / Sign up

Export Citation Format

Share Document