z-logo
Premium
Miscibility and melting behavior of poly(ethylene terephthalate)/poly(trimethylene terephthalate) blends
Author(s) -
Liang Hao,
Xie Fang,
Chen Biao,
Guo Fuquan,
Jin Zhen,
Luo Fusheng
Publication year - 2007
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.27081
Subject(s) - miscibility , materials science , differential scanning calorimetry , melting point depression , glass transition , polymer blend , crystallization , polymer chemistry , amorphous solid , polymer , melting point , chemical engineering , thermodynamics , composite material , copolymer , crystallography , chemistry , physics , engineering
The miscibility and melting behavior of binary crystalline blends of poly(ethylene terephthalate) (PET)/poly(trimethylene terephthalate) (PTT) have been investigated with differential scanning calorimetry and scanning electron microscope. The blends exhibit a single composition‐dependent glass transition temperature ( T g ) and the measured T g fit well with the predicted T g value by the Fox equation and Gordon‐Taylor equation. In addition to that, a single composition‐dependent cold crystallization temperature ( T cc ) value can be observed and it decreases nearly linearly with the low T g component, PTT, which can also be taken as a valid supportive evidence for miscibility. The SEM graphs showed complete homogeneity in the fractured surfaces of the quenched PET/PTT blends, which provided morphology evidence of a total miscibility of PET/PTT blend in amorphous state at all compositions. The polymer–polymer interaction parameter, χ 12 , calculated from equilibrium melting temperature depression of the PET component was −0.1634, revealing miscibility of PET/PTT blends in the melting state. The melting crystallization temperature ( T mc ) of the blends decreased with an increase of the minor component and the 50/50 sample showed the lowest T mc value, which is also related to its miscible nature in the melting state. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom