Synthesis and characterization of poly(ester ether siloxane)s

• DOI: 10.1002/pi.2085
• Publication Date: 2006-06-13T11:32:49Z
• Authors: Marija V Vuckovic; Vesna V Antic; Biljana P Dojcinovic; Milutin N Govedarica; Jasna Djonlagic
• Keywords: thermoplastic elastomers; Poly(ester ether siloxane)s; α-ω-dihydroxy-poly(propyleneoxide-dimethyl-siloxane- propyleneoxide); α,ω-dihydroxy-poly(propyleneoxide-dimethylsiloxane-propyleneoxide); poly(ester ether siloxane)s; 01 natural sciences; Thermoplastic elastomers; 0104 chemical sciences

AbstractA series of novel thermoplastic elastomers based on ABA‐type triblock prepolymers, poly[(propylene oxide)–(dimethylsiloxane)–(propylene oxide)] (PPO‐PDMS‐PPO), as the soft segments, and poly(butylene terephthalate) (PBT), as the hard segments, was synthesized by catalyzed two‐step melt transesterification of dimethyl terephthalate (DMT) with 1,4‐butanediol (BD) and α,ω‐dihydroxy‐(PPO‐PDMS‐PPO) (M̄n = 2930 g mol−1). Several copolymers with a content of hard PBT segments between 40 and 60 mass% and a constant length of the soft PPO‐PDMS‐PPO segments were prepared. The siloxane‐containing triblock prepolymer with hydrophilic terminal PPO blocks was used to improve the compatibility between the polar comonomers, i.e. DMT and BD, and the non‐polar PDMS segments. The structure and composition of the copolymers were examined using 1H NMR spectroscopy, while the effectiveness of the incorporation of α,ω‐dihydroxy‐(PPO‐PDMS‐PPO) prepolymer into the copolyester chains was controlled by chloroform extraction. The effect of the structure and composition of the copolymers on the transition temperatures (Tm and Tg) and the thermal and thermo‐oxidative degradation stability, as well as on the degree of crystallinity, and some rheological properties, were studied. Copyright © 2006 Society of Chemical Industry