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UCST Type Phase Boundary and Accelerated Crystallization in PTT/PET Blends.
Kousuke Sugeno1, Satoshi Kokubun1, Hiromu Saito1
1Department of Organic and Polymer Materials Chemistry, Tokyo University of Agriculture and Technology, Koganei-shi, Tokyo 184-8588, Japan.
Blending poly(trimethylene terephthalate) (PTT) and poly(ethylene terephthalate) (PET) accelerates crystallization and reduces spherulite size. This occurs due to liquid-liquid phase separation, creating interconnected structures below the transition temperature.
Area of Science:
- Polymer Science
- Materials Science
- Physical Chemistry
Background:
- Poly(trimethylene terephthalate) (PTT) and poly(ethylene terephthalate) (PET) are widely used polyesters.
- Understanding their blend behavior is crucial for developing novel materials with tailored properties.
- Crystallization kinetics significantly influence the final morphology and performance of polymer blends.
Purpose of the Study:
- To investigate the structure development and crystallization kinetics of PTT/PET blends.
- To determine the effect of blending on crystallization behavior compared to neat polymers.
- To elucidate the underlying mechanisms driving the observed changes in crystallization.
Main Methods:
- Polarized optical microscopy to observe morphology and spherulite growth.
- Light scattering to analyze crystallization kinetics and structure evolution.
- Melt crystallization at controlled temperatures (e.g., 180 °C).
Main Results:
- Blend crystallization was faster with smaller spherulites than neat PTT or PET.
- A discontinuous gap in crystallization time indicated a phase transition temperature (T_tr), e.g., 215 °C for 60/40 PTT/PET.
- Crystallization acceleration was linked to enhanced nucleation rates and interconnected tiny spherulites below T_tr.
Conclusions:
- PTT/PET blends exhibit accelerated crystallization and finer structures compared to individual polymers.
- Liquid-liquid phase separation, likely via spinodal decomposition due to an upper critical solution temperature (UCST), drives these changes.
- The findings suggest potential for creating advanced polymer materials with controlled morphology through strategic blending.
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