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首页> 外文期刊>Journal of Macromolecular Science. Physics >Crystallization behavior of poly(trimethylene terephthalate)/polycarbonate blends
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Crystallization behavior of poly(trimethylene terephthalate)/polycarbonate blends

机译:聚对苯二甲酸丙二醇酯/聚碳酸酯共混物的结晶行为

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摘要

The crystallization behavior of poly(trimethylene terephthalate (PTT) in compatibilized and uncompatibilized PTT/polycarbonate (PC) blends are investigated in the research reported in this paper. The differential scanning calorimetry (DSC) results showed that the crystallization behaviors of PTT/PC blends were very sensitive to PC content. The onset (T-ci) and the peak (T-c) crystallization temperatures shifted to lower temperatures whereas the area of the exotherm decreased quickly as the PC content was increased. The Avrami exponent, n, decreased from 4.32 to 3.61 as the PC content was increased from 0 to 20 wt %, and the growth rate constant, Z(c), decreased gradually as well. This suggests that the nucleation mechanism exhibits the tendency of changing gradually from a thermal nucleation to an athermal mode although the growth mechanism still remains three-dimensional. When epoxy (2.7 phr) was added as a compatibilizer during melt blending, the T-ci and Tc shifted slightly to higher temperature (<= 2 degrees C), and the crystallization enthalpy, however, exhibited an increased crystallinity with the exception of the 90/10/2.7phr PTT/ PC/Epoxy. This suggests that the epoxy make a positive contribution to the PTT crystallization. Moreover, the influences of epoxy on the crystallization behaviors of PTT/ PC blends are related to the epoxy content. By contrast, the compatibilizer of ethylene-propylene-diene copolymer graft glycidyl methacrylate (EPDM-g-GMA, <= 6.3 phr) had little effect on the crystallization behavior of PTT/PC blends. For PTT/PC/Epoxy (2.7phr) blends, the Avrami exponent, n, decreased to near 3, while the growth rate constant, Z(c), increased slightly as PC content was increased from 0 to 20 wt %. It is suggested that epoxy accelerated the process of the nucleation mechanism changing from thermal nucleation to an. athermal mode. The EPDM-g-GMA had little effect on the nucleation mode and spherical growth mechanism. The PTT spherulite morphologies in PTT/PC blends were very sensitive to blend composition. Completely different morphologies were observed in pure PTT, PTT/PC, PTT/PC/Epoxy, and PTT/PC/EPDM-g-GMA blends.
机译:本文研究了在相容和不相容的PTT /聚碳酸酯(PC)共混物中聚对苯二甲酸丙二醇酯(PTT)的结晶行为,差示扫描量热法(DSC)结果表明,PTT / PC共混物的结晶行为对PC含量非常敏感,开始温度(T-ci)和峰值(Tc)转变为较低的温度,而放热面积随PC含量的增加而迅速降低,Avrami指数n从4.32降低。 PC含量从0增加到20 wt%时,Pb为3.61,生长速率常数Z(c)也逐渐降低,这表明成核机理呈现出从热成核向无热成核的趋势。增长模式仍然保持三维模式,当在熔融共混过程中添加环氧树脂(2.7 phr)作为增容剂时,T-ci和Tc略有升高r温度(<= 2摄氏度)和结晶焓显示出增加的结晶度,除了90/10 / 2.7phr PTT / PC /环氧树脂。这表明环氧树脂对PTT结晶起到了积极的作用。此外,环氧树脂对PTT / PC共混物结晶行为的影响与环氧树脂含量有关。相比之下,乙烯-丙烯-二烯共聚物接枝的甲基丙烯酸缩水甘油酯(EPDM-g-GMA,<= 6.3 phr)的增容剂对PTT / PC共混物的结晶行为影响很小。对于PTT / PC /环氧树脂(2.7phr)混合物,随着PC含量从0到20 wt%的增加,Avrami指数n降低至接近3,而增长率常数Z(c)则略有增加。提示环氧树脂促进了成核机理从热成核转变为成核的过程。无热模式。 EPDM-g-GMA对成核方式和球形生长机理影响很小。 PTT / PC混合物中的PTT球晶形态对混合物组成非常敏感。在纯PTT,PTT / PC,PTT / PC /环氧树脂和PTT / PC / EPDM-g-GMA共混物中观察到完全不同的形态。

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