Crystallization of poly(ethylene terephthalate) modified with codiols

Abstract

AbstractThe nucleation of poly(ethylene terephthalate) (PET) by codiols and olefinic segments was studied. The codiols 1,5‐pentanediol, 1,8‐octanediol, 2,5‐hexanediol, and 1,3‐dihydroxymethyl benzene were copolymerized into PET in a concentration range of 0–10 mol %. The melting (Tm), crystallization (Tc), and glass‐transition (Tg) temperatures were studied. These codiols were found to be able to nucleate PET at low concentrations, probably by lowering the surface free energy of the chain fold. However, the codiols also disturbed the structural order of the polymer, resulting in a decrease in both the Tm and Tc values. The optimum codiol concentration was found to be at around 1 mol %, which is lower than previously reported. A diamide segment N,N′‐bis(p‐carbo‐methoxybenzoyl)ethanediamine (T2T) was found to be a more effective nucleator than the codiols; however, no synergy was observed between the nucleating effect of the diamide segment T2T and that of the codiol. An olefinic diol (C36‐diol) with a molecular weight of 540 g/mol was also copolymerized into PET in a concentration range of 0–21 wt %. Only one Tg was observed in the resulting copolymers, suggesting that the amorphous phases of PET and the C36‐diol are miscible. The main effect of incorporating the C36‐diol into PET was the lowering of the Tg; thus, the C36‐diol is an internal plastifier for PET. The C36‐diol had little effect on the Tm value; however, the Tc value actually increased in the 11.5 wt % copolymer. As the Tg decreased and the Tc increased, the crystallization window also increased and thereby the likelihood of crystallization. Therefore, the thermally stable C36‐diol appears to be an interesting compound that may be useful in improving the crystallization of PET. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 2676–2682, 2001