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Microhardness of condensation polymers and copolymers. 2. Poly(ester ether carbonate) thermoplastic terpolymers

 

作者: F.J. Baltá Calleja,   S. Fakirov,   Z. Roslaniec,   M. Krumova,   T.A. Ezquerra,   D.R. Rueda,  

 

期刊: Journal of Macromolecular Science, Part B  (Taylor Available online 1998)
卷期: Volume 37, issue 2  

页码: 219-237

 

ISSN:0022-2348

 

年代: 1998

 

DOI:10.1080/00222349808220468

 

出版商: Taylor & Francis Group

 

关键词: Thermoplastic elastomers;Terpolymers;Microhardness;Soft segments;Hard segments;Crystallinity

 

数据来源: Taylor

 

摘要:

The number of phases, transition temperatures, and microhardness of a series of poly(ester ether carbonate) (PEEC) multiblock terpolymers with poly(butylene terephthalate) (PBT) hard segments have been investigated as a function of ether/carbonate (EC) soft-segment composition at constant PBT content. The polymerization degree of PBT and the intrinsic viscosity of the terpolymers were determined by viscosimetry. The degree of crystal-Unity, long spacing, glass transitionsTg, and melting temperature were derived by means of x-ray diffraction, dynamic mechanical thermal analysis (DMTA), and differential scanning calorimetry (DSC) measurements. Surface mechanical properties were studied by microindentation tests. It was found that the terpolymer consists of two amorphous (EC and PBT) phases and one crystalline (PBT) phase. TheTgvalue of PBT does not depend on the chemical composition of the soft segments, in the contrast to theTgof the soft-segment amorphous phase. Introduction of polycarbonate moities in the soft segments induces an increase ofTgby 50°C without formation of an additional (third) amorphous phase. The reduced crystallizability of PBT hard segments (by a factor of 3) is explained by this decrease of flexibility of the soft segments, which also causes a twofold reduction in the microhardness values. The dominating contribution of crystallinity to the microhardness is shown. However, the much lower measured overall microhardness in contrast to the one calculated by means of the additive law is explained by the plasticizing effect of the soft amorphous phase. This assumption is in agreement with the structure model derived from the small-angle x-ray (SAXS) and wide-angle x-ray (WAXS) data.

 

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