The melting behavior of isothermally crystallized PET has been studied using linear heating in a differential scanning calorimeter (DSC). Variables such as crystallization temperature, crystallization time, heating rate, and average molecular weight are the main focus of the study. On the basis of s
Influence of molecular weight on the ordered state in poly(ethylene terephthalate)
โ Scribed by M. V. S. Rao; N. E. Dweltz
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 500 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
WAXS, DSC, and IR methods have been employed to follow the crystallization of poly(ethy1ene terephthalate) as a function of molecular weight. The degree of order, which is a measure of the extent of crystallization, decreased with increasing molecular weight. The degree of reduction in the molecular order with increasing molecular weight differed depending on the technique employed to measure it. Crystallinity indices obtained by x-ray diffraction methods show an almost linear relationship with molecular weight. The Trans-Gauche ratio inferred from the IR spectrum tends to decrease at a very rapid rate with increasing molecular weight. The heat of fusion, computed from the melting endotherm in DSC thermograms, shows a smaller but a defmite decreasing trend with increasing molecular weight. Besides, the thermograms themselves showed distinct changes related to the molecular weight differences. The results have been discussed in terms of two different possible influencing factors known to affect the crystallization procesa in almost all polymers. Up to certain molecular weights, random coiling of molecules appears to be the more dominant factor, but in a much higher range of molecular weights, entanglement in the molecular network may become predominant.
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