scholarly journals Thermomechanical and Morphological Properties of Poly(ethylene terephthalate)/Anhydrous Calcium Terephthalate Nanocomposites

Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 276 ◽  
Author(s):  
Franco Dominici ◽  
Fabrizio Sarasini ◽  
Francesca Luzi ◽  
Luigi Torre ◽  
Debora Puglia

Calcium terephthalate anhydrous salts (CATAS), synthetized by reaction of terephthalic acid with metal (Ca) oxide were incorporated at different weight contents (0–30 wt. %) in recycled Poly(ethylene terephthalate) (rPET) by melt processing. Their structure, morphology, thermal and mechanical properties (tensile and flexural behavior) were investigated. Results of tensile strength of the different formulations showed that when the CATAS content increased from 0.1 to 0.4 wt. %, tangible changes were observed (variation of tensile strength from 65.5 to 69.4 MPa, increasing value for E from 2887 up to 3131 MPa, respectively for neat rPET and rPET_0.4CATAS). A threshold weight amount (0.4 wt. %) of CATAS was also found, by formation at low loading, of a rigid amorphous fraction at the rPET/CATAS interface, due to the aromatic interactions (π−π conjugation) between the matrix and the filler. Above the threshold, a restriction of rPET/CATAS molecular chains mobility was detected, due to the formation of hybrid mechanical percolation networks. Additionally, enhanced thermal stability of CATAS filled rPET was registered at high content (Tmax shift from 426 to 441 °C, respectively, for rPET and rPET_30CATAS), essentially due to chemical compatibility between terephthalate salts and polymer molecules, rich in stable aromatic rings. The singularity of a cold crystallization event, identified at the same loading level, confirmed the presence of an equilibrium state between nucleation and blocking effect of amorphous phase, basically related to the characteristic common terephthalate structure of synthetized Ca–Metal Organic Framework and the rPET matrix.

2006 ◽  
Vol 91 (4) ◽  
pp. 875-885 ◽  
Author(s):  
Calin Flaviu Ladasiu Ciolacu ◽  
Namita Roy Choudhury ◽  
Naba K. Dutta

1997 ◽  
Vol 67 (12) ◽  
pp. 891-896 ◽  
Author(s):  
Daw-Ming Fann ◽  
Steve K. Huang ◽  
Jiunn-Yih Lee

Recycled poly (ethylene terephthalate) (r-pet) used in blends with a fiber grade material (f-pet) is investigated. As-spun fibers of r-pet, f-pet, and r/f-pet blends are made at winding speeds ranging from 1000 to 4000 m/min (mpm), with subsequent drawing in the range of 1.6 to 4.0×. Spinning and drawing behaviors of the fibers are analyzed using orientation (birefringence), boil-off shrinkage, calorimetric (dsc), and mechanical measurements. The fully oriented yarns from the r-pet show a tensile strength of 70% of the fiber grade, with 3.2 g/d (r-pet) to 4.6 g/d (f-pet), which still meets and surpasses minimum industrial requirements. The dsc study of these materials indicates that the decreased crystallinity of the r-pet may be the main cause for the decreased tensile strength of the product.


1993 ◽  
Vol 321 ◽  
Author(s):  
Veronika E. Reinsch ◽  
Ludwig Rebenfeld

ABSTRACTBlends of poly (ethylene terephthalate), or PET, and polycarbonate (PC) over a range of compositions were studied in isothermal crystallizations from the melt using differential scanning calorimetry (DSC). Both crystallization rate and degree of crystallinity of PET depend on blend composition. The glass transition temperature, Tg, of PET and PC in blends and pure polymer were also measured by DSC. Elevation of the Tg of PET and depression of the Tg of PC are observed upon blending. In cooling scans, dynamic crystallization from the melt was observed. In PET/PC blends with high PC content, a novel dual-peak crystallization of PET was observed. The effects of thermal history on crystallization kinetics and degree of crystallinity were also determined in isothermal crystallization studies. For Melt processing times between 1 and 30 Min and for processing temperatures between 280 and 300 °C, Melt processing temperature was seen to have a stronger effect than processing time.


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