Abstract
AbstractThe homopolymers, poly(3,3‐bisethoxymethyl oxetane) (polyBEMO), poly(3,3‐bisazidomethyl oxetane) (polyBAMO), and triblock copolymers based on these homopolymers and a statistical copolymer center block composed of BAMO and 3‐azidomethyl‐3‐methyl oxetane AMMO were synthesized and characterized by differential scanning calorimetry, modulus‐temperature, optical microscopy, membrane osmometry, and solution and melt viscosity. The values of K and a for the Mark‐Houwink equation were found to be 7.29 × 10−3 mL/g and 0.80, respectively, for polyBEMO at 25°C using number‐average molecular weights. Glass transition temperatures were in the range −25 to −40°C and melting temperatures were between 65 and 90°C for all polymers. The melting temperature was found to increase as expected with molecular weight. Melt viscosities of triblock copolymers with polyBAMO end blocks were at least an order of magnitude lower than those with polyBEMO end blocks and clear optically, suggesting that the polyBAMO‐based triblock copolymers formed one phase in the melt, while the polyBEMO‐based triblock materials (milk white) phase separated. The addition of filler raised the melt viscosity to a level between that predicted by the Guth‐Smallwood and the Mooney equations.
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