Temperature dependence of the rigid amorphous fraction in poly(ethylene terephthalate)

2014 ◽  
Vol 58 ◽  
pp. 60-68 ◽  
Author(s):  
Maria Cristina Righetti ◽  
Michele Laus ◽  
Maria Laura Di Lorenzo
2010 ◽  
Vol 43 (18) ◽  
pp. 7689-7694 ◽  
Author(s):  
Maria Laura Di Lorenzo ◽  
Maria Cristina Righetti ◽  
Mariacristina Cocca ◽  
Bernhard Wunderlich

e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Maria Cristina Righetti ◽  
Maria Laura Di Lorenzo

AbstractVitrification and devitrification of the rigid amorphous fraction (RAF) of poly(ethylene terephthalate) (PET), analyzed during development and disappearance of the three phase structure, are detailed in this contribution. Upon cooling from the melt at a constant rate, the rigid amorphous fraction starts to vitrify when the crystallization process is almost finished, and continues on further cooling. The rigid amorphous fraction is formed in the same temperature range of the secondary crystal growth. Analysis of the low melting endotherm that is observed in isothermally crystallized PET a few degrees above the crystallization temperature reveals a joint contribution of melting and devitrification of the rigid amorphous fraction. The results confirm a link between secondary crystallization and vitrification of the rigid amorphous fraction in semicrystalline polymers. Secondary crystallization takes place in geometrically restricted areas, in which the polymer chains undergo large constraints, so that the mobility of the amorphous chain portions coupled with the crystal phase is reduced. Similarly, the gain in mobility upon partial melting of thinner and/or more defective crystals allows an increase in mobility of the coupled amorphous regions, which results in concurrent mobilization of the rigid amorphous fraction.


RSC Advances ◽  
2021 ◽  
Vol 11 (41) ◽  
pp. 25731-25737
Author(s):  
Maria Cristina Righetti ◽  
Maria Laura Di Lorenzo ◽  
Patrizia Cinelli ◽  
Massimo Gazzano

At room temperature and at the human body temperature, all the amorphous fraction is mobile in poly(butylene succinate).


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