New catalysts for poly(ethylene terephthalate)-bisphenol a polycarbonate reactive blending

1995 ◽  
Vol 55 (8) ◽  
pp. 1157-1163 ◽  
Author(s):  
Maurizio Fiorini ◽  
Corrado Berti ◽  
Vladimir Ignatov ◽  
Maurizio Toselli ◽  
Francesco Pilati
2011 ◽  
Vol 214 ◽  
pp. 301-305
Author(s):  
Jun Lu ◽  
Jiao Jiao Tian ◽  
Dao Peng Zhang ◽  
Rui Huang

With a combination of three-dimensional crystal ordering and long-chain molecular orientational ordering, the extended-chain crystals of polymers are ideal system for the studies on low-dimensional physics, and have potential applications as functional components. In this study, poly (ethylene terephthalate) / bisphenol-A polycarbonate (PET/BAPC) blend samples were prepared with solid phase forming technique under high pressure, and extended-chain single crystals with large c-axis thickness were formed within a relative short time. The fracture and deformation behaviors of the grownup crystals were investigated using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Morphological observation showed that most of the extended-chain crystals were endowed with perfect appearance after the sample fracture. However, there were still a few crystals fractured apart, along or perpendicularly to their c-axis direction, or with cohesive fracture surfaces. Fractured spherulites with extended-chain lamellae as substructures were also disclosed in extended-chain crystals with AFM. Furthermore, the parallel lamellae deformed and changed their striation direction during the crystal growth, as was observed on a kind of extended-chain crystals grown in a PET oligomer and BAPC blend (PETO/BAPC). This study may be instructive to the improvement of the separation technique of such single crystals, so as to hasten their real applications.


2011 ◽  
Vol 213 ◽  
pp. 470-474
Author(s):  
Jun Lu ◽  
Dao Peng Zhang ◽  
Jiao Jiao Tian ◽  
Rui Huang

The high-pressure crystallized poly (ethylene terephthalate) / bisphenol-A polycarbonate (PET/BAPC) blend samples were investigated using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Besides the extended-chain single crystals with high quality and large c-axis thickness, the results showed that some novel crystal morphologies were formed in the multi-phase system within a relative short time. Spherulitic structures with different characteristics were observed, in and out the cultured polyester extended-chain crystals, respectively, and their substructures were found to be extended-chain lamellae. Furthermore, bud-like nano-crystals with zero- or one-dimensional structures, some of which aggregated and then evolved into three-dimensional nano-dendrites, were grown during the cooling process of the polyester blends at high pressure. The disclosed entities during this study may promote the understanding of formation process and mechanism for both spherulite and extended-chain crystals of polyesters, so as to instruct the processing of such alloyed engineering plastics with high performance.


2010 ◽  
Vol 654-656 ◽  
pp. 2632-2635
Author(s):  
Jun Lu ◽  
Dai Kun Xi ◽  
Rui Huang

In this study, the crystallization behaviors of the poly (ethylene terephthalate) oligomer/bisphenol-A polycarbonate (PETO/BAPC) blends were investigated under high pressure, and the recovered PETO/BAPC samples were characterized using XRD, DSC, SEM and AFM. The results showed that high-quality extended-chain single crystals with large c-axis thickness were formed in the multi-phase system within a relative short time, and the inner defects of the disclosed crystals could be removed by a self-healing process through high-temperature and high-pressure annealing. Morphologies of extended-chain crystals with different characteristics were also revealed with SEM and AFM. Wedge-shaped and bent extended-chain morphologies suggested that sliding diffusion and transesterification occurred simultaneously in the system, and the crystallization of the large crystals was a self-assembling process induced by chemical reactions at high pressure. This process provides a new route to grow large polymer extended-chain crystals and suggests self-assembly under high pressure is a promising method to create materials with new structures and properties.


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