Influence of hyperbranched against linear architecture on crystallization behavior of poly(ɛ-caprolactone)s in binary blends with poly(vinyl chloride)

2007 ◽  
Vol 45 (5) ◽  
pp. 577-589 ◽  
Author(s):  
Jeongsoo Choi ◽  
Sang-Wook Chun ◽  
Seung-Yeop Kwak
2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Mei Chan Sin ◽  
Irene Kit Ping Tan ◽  
Mohd Suffian Mohd Annuar ◽  
Seng Neon Gan

Plasticized poly(vinyl chloride) (PVC) is one of the most widely consumed commodity plastics. Nevertheless, the commonly used plasticizers, particularly phthalates, are found to be detrimental to the environment and human health. This study aimed to investigate the ability of an alternative greener material, medium-chain-length polyhydroxyalkanoates (mcl-PHA), a kind of biopolyester and its thermally degraded oligoesters, to act as a compatible bioplasticizer for PVC. In this study, mcl-PHA were synthesized byPseudomonas putidaPGA1 in shake flask fermentation using saponified palm kernel oil (SPKO) and subsequently moderately thermodegraded to low molecular weight oligoesters (degPHA). SEM, ATR-FTIR,1H-NMR, and DMA were conducted to study the film morphology, microstructure, miscibility, and viscoelastic properties of the PVC-PHA and PVC/degPHA binary blends. Increased height and sharpness of tanδmax⁡peak for all binary blends reveal an increase in chain mobility in the PVC matrix and high miscibility within the system. The PVC-PHA miscibility is possibly due to the presence of specific interactions between chlorines of PVC with the C=O group of PHA as evidenced by spectroscopic analyses. Dynamic viscoelastic measurements also showed that mcl-PHA and their oligoesters could reduce theTgof PVC, imparting elasticity to the PVC compounds and decreasing the stiffness of PVC.


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