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聚对苯二甲酸丙二醇酯/聚碳酸酯共混物反应诱导混溶性的研究

A study on reaction-induced miscibility of poly(trimethylene terephthalate)/polycarbonate blends.

作者信息

Aravind Indose, Eichhorn Klaus-Jochen, Komber Hartmut, Jehnichen Dieter, Zafeiropoulos N E, Ahn Kyung Hyun, Grohens Yves, Stamm Manfred, Thomas Sabu

机构信息

School of Chemical Sciences, Mahatma Gandhi University, Priyadarshini Hills P.O., Kottayam, Kerala, India 686 560.

出版信息

J Phys Chem B. 2009 Feb 12;113(6):1569-78. doi: 10.1021/jp805204m.

Abstract

The effect of annealing on the miscibility and phase behavior of Sorona {poly(trimethylene terephthalate), PTT} and bisphenol A polycarbonate (PC) blends was examined. These blends exhibited heterogeneous phase-separated morphology and two well-spaced glass transition temperatures (Tgs) indicating immiscibility. The Sorona/PC blends were thermally annealed at 260 degrees C for different times to induce various extents of transreactions between the two polymers. After annealing at high temperature the original two Tgs of blends were found to merge into one single Tg, exhibiting a homogeneous morphology. It is interesting to note that upon extended annealing the original semicrystalline morphology transformed into an amorphous nature. This is attributed to chemical transreactions between the PTT and PC chain segments as evidenced with FTIR, DSC, DMA, 1H NMR, and WAXS measurements. A new characteristic aryl C-O-C vibration band present at 1070 cm(-1) in the FTIR spectra of the annealed blends indicated the formation of an aromatic polyester structure due to the transreactions between PTT and PC. The sequence structures of the produced copolyesters were determined by a NMR triad analysis, which showed that the randomness increased with time of heating. WAXS analysis confirmed that the PTT/PC blends completely lost their crystallinity when annealed at 260 degrees C for a period of 120 min or longer, indicating the formation of fully random copolyesters. A random copolymer formed as a result of the transreactions between PTT and PC serves as a compatibilizer at the beginning, and upon extended annealing this became the main species of the system which is finally transformed to a homogeneous and amorphous phase.

摘要

研究了退火对索罗纳(聚对苯二甲酸丙二醇酯,PTT)与双酚A聚碳酸酯(PC)共混物的混溶性和相行为的影响。这些共混物呈现出非均相相分离形态以及两个间隔明显的玻璃化转变温度(Tg),表明它们互不相溶。将索罗纳/PC共混物在260℃下进行不同时间的热退火,以引发两种聚合物之间不同程度的转反应。在高温退火后,发现共混物原来的两个Tg合并为一个单一的Tg,呈现出均匀的形态。值得注意的是,经过长时间退火后,原来的半结晶形态转变为非晶态。这归因于PTT和PC链段之间的化学转反应,傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、动态热机械分析(DMA)、核磁共振氢谱(1H NMR)和广角X射线散射(WAXS)测量结果证明了这一点。退火共混物的FTIR光谱中在1070 cm-1处出现的新的特征芳基C-O-C振动带表明,由于PTT和PC之间的转反应形成了一种芳香族聚酯结构。通过核磁共振三元组分析确定了所生成共聚酯的序列结构,结果表明无规度随加热时间增加。WAXS分析证实,当在260℃下退火120分钟或更长时间时,PTT/PC共混物完全失去其结晶度,表明形成了完全无规的共聚酯。PTT和PC之间的转反应形成的无规共聚物一开始起到增容剂的作用,经过长时间退火后,它成为体系的主要成分,最终转变为均匀的非晶相。

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