Hydroxy-Terminated Poly(epsilon-caprolactone-co-delta-valerolactone) Oligomers: Synthesis, Characterization, and Polyurethane Network Formation
Polymers and High Performance Materials
Difunctional hydroxy-terminated poly (epsilon-caprolactone-co-delta-valerolactone) (PCV) oligomers were synthesized by the diol-initiated bulk copolymerization of epsilon-caprolactone (C) and delta-valerolactone (V). The two homopolymers were semicrystalline, with almost identical melting temperatures; copolymerization significantly lowered the melting point (T(m)) compared to either homopolymer. Copolymer melting points were found to decrease with decreasing molecular weight and to be dependent on composition, i.e., the incorporation of a comonomer into either homopolymer resulted in a decrease in T(m), with the maximum decrease occurring at a copolymer composition of about 60 mol % epsilon-caprolactone. The molar compositions of the copolyesters were determined from C-13-NMR spectra. The reactivity ratios of the two monomers (M1 = C, M2 = V) were determined to be r1 = 0.25 and r2 = 0.49. Number average molecular weight (MBARn) of the PCV diols was inversely proportional to the initial diol concentration within the studied molecular weight range of 900 to 11,100 g/mol. Crosslinked polyurethane networks were prepared by reacting PCV diols with triphenylmethane triisocyanate. Network characterization included determination of sol content by solvent extraction, glass transition (T(g)) and T(m) by DSC, and tensile properties by stress-strain measurements. Completely amorphous networks resulted from PCV diols of M(n)BAR less-than-or-equal-to 2,400; semicrystalline networks resulted from PCV diols of M(n)BAR greater-than-or-equal-to 3,600.
Journal of Polymer Science Part A: Polymer Chemistry
Storey, R. F.,
Herring, K. R.,
Hoffman, D. C.
(1991). Hydroxy-Terminated Poly(epsilon-caprolactone-co-delta-valerolactone) Oligomers: Synthesis, Characterization, and Polyurethane Network Formation. Journal of Polymer Science Part A: Polymer Chemistry, 29(12), 1759-1777.
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