Sequential reordering in condensation copolymers, 2. Melting- and crystallization-induced sequential reordering in miscible poly(butylene terephthalate)/polyarylate blends

• Published in: Macromolecular chemistry and physics 1996-09, Vol.197 (9), p.2869-2887
• Main Authors: Denchev, Zlatan, Sarkissova, Marianna, Fakirov, Stoyko, Yilmaz, Ferdane
• Format: Article
• Language: English
• Subjects: Applied sciences; Chemical modifications; Chemical reactions and properties; Exact sciences and technology; Organic polymers; Physicochemistry of polymers
• ISSN: 1022-1352; 1521-3935
• DOI: 10.1002/macp.1996.021970922

A 50/50 (weight ratio (38/62 mole ratio referred to repeating units)) blend of poly(butylene terephthalate) (PBT) and polyarylate (PAr), was studied by means of thermal, solubility, X‐ray and nuclear magnetic resonance techniques after annealing procedures that enable transesterification. Prolonged thermal treatment at 290°C gives rise to a copolymer that no longer reveals melting or crystallization. In accordance with previous reports, this effect is attributed to the formation of a random copolymer. Additional annealing of such samples at the relatively low temperature of 140°C results in the reappearance of melting endotherms in the differential scanning calorimetry curves. This effect is explained by crystallization‐induced sequential reordering from random to block copolymer by means of transreactions. In that way a PBT/PAr blend was shown to be another polymer system, along with poly(ethylene terephthalate) (PET)/polycarbonate (PC) and PET/PAr blends, in which the entire cycle is realized, from two homopolymers via a block‐ and random copolymer to a block copolymer. The unusually low temperature at which the crystallization‐induced sequential reordering to block polymers takes place is explained by the miscibility of PBT and PAr which enables transreactions to take place in the bulk.