Kandilioti Georgia, Govaris Giannis K, Gregoriou Vasilis G
Foundation for Research and Technology-Hellas, Institute of Chemical Engineering and High Temperature Chemical Processes (FORTH-ICEHT), P.O. Box 1414, Stadiou Street, Patras, 26504 Greece.
Appl Spectrosc. 2004 Sep;58(9):1082-92. doi: 10.1366/0003702041959352.
The origin of the phenomenon of stress oscillation during step-wise stretching at room temperature for amorphous poly(ethylene terephthalate) (PET) was investigated using vibrational spectroscopy. For the first time, transmission Fourier transform infrared (FT-IR), attenuated total reflection (ATR) FT-IR, and micro-Raman spectroscopies were used in order to investigate the correlation of the orientation of the molecular chains, their conformational transformations, and the appearance of stress-induced crystallization to the phenomenon of stress oscillation during the step-wise stretching procedure. The phenomenon of stress oscillation occurs when amorphous PET is exposed to mechanical stress during which the extension rate is increased in a step-wise manner. This phenomenon leads to the formation of a pattern of opaque and transparent stripes (''striated'' or oscillating region), clearly distinguished from the unstretched (''bulk'') and the ''necking'' regions. Both infrared and Raman spectroscopic investigations revealed that the main conformational transformations and a significant increase of the crystallinity occur simultaneously in the ''striated'' region. Polarized infrared experiments showed the presence of increased molecular orientation, which is more profound for the ''intense striated'' region. Finally, micro-Raman spectroscopy allowed the study of opaque and transparent stripes individually and showed that the opaque stripes are more crystalline. Thus, our findings provide conclusive experimental support for the theory, which directly correlates the appearance of the stress-oscillation phenomenon with the induction of crystallinity and heat release and is based on Barenblatt's model. Our study also provides new conformational assignments for the infrared bands in PET for the high-frequency region from 3200 to 3800 cm(-1). Specifically, the bands at 3336 cm(-1) and at 3298 cm(-1) have been attributed to the trans and gauche conformations, respectively.
利用振动光谱研究了室温下非晶态聚对苯二甲酸乙二酯(PET)在逐步拉伸过程中应力振荡现象的起源。首次使用透射傅里叶变换红外光谱(FT-IR)、衰减全反射(ATR)FT-IR和显微拉曼光谱,以研究分子链取向、其构象转变以及应力诱导结晶的出现与逐步拉伸过程中应力振荡现象之间的相关性。当非晶态PET在逐步增加拉伸速率的机械应力作用下时,会出现应力振荡现象。这种现象导致形成不透明和透明条纹的图案(“条纹状”或振荡区域),与未拉伸(“本体”)和“颈缩”区域明显区分。红外和拉曼光谱研究均表明,在“条纹状”区域同时发生主要的构象转变和结晶度的显著增加。偏振红外实验表明存在分子取向增加的情况,这在“强条纹状”区域更为明显。最后,显微拉曼光谱能够分别研究不透明和透明条纹,并表明不透明条纹的结晶度更高。因此,我们的研究结果为该理论提供了确凿的实验支持,该理论直接将应力振荡现象的出现与结晶度的诱导和热释放相关联,并且基于巴伦布拉特模型。我们的研究还为PET在3200至3800 cm(-1)高频区域的红外波段提供了新的构象归属。具体而言,3336 cm(-1)和3298 cm(-1)处的波段分别归因于反式和顺式构象。