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Crystallization kinetics of poly(trimethylene terephthalate)/poly(ether imide) blends
Author(s) -
Chiu HsiuJung,
Shu WeiJye,
Huang JiehMing
Publication year - 2006
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.20411
Subject(s) - materials science , crystallization , nucleation , differential scanning calorimetry , glass transition , polymer chemistry , ether , imide , chemical engineering , kinetics , composite material , polymer , thermodynamics , organic chemistry , chemistry , physics , quantum mechanics , engineering
The crystallization kinetics of a melt‐miscible blend, consisting of poly(trimethylene terephthalate) (PTT) and poly(ether imide) (PEI) prepared by solution precipitation, has been investigated by means of optical polarized microscopy and differential scanning calorimeter. It was found that both the PTT spherulitic growth rate ( G ) and overall crystallization rate constant ( k n ) were depressed, with increasing PEI composition or crystallization temperature ( T c ). The kinetic retardation was attributed to the decrease in PTT molecular mobility, and the dilution of PTT concentration due to the addition of PEI, which has a higher glass transition temperature ( T g ). According to the Lauritzen–Hoffman theory of secondary nucleation, the crystallization of PTT in blends was similar to that of neat PTT as regime III, n = 4 and regime II, n = 2 growth processes, while the transition point of regime III to II has been shifted from 194°C for neat PTT to 190°C for blends. POLYM. ENG. SCI. 46:89–96, 2006. © 2005 Society of Plastics Engineers