Abstract
Ring opening transesterification polymerization of lactones derived from menthone and carvomenthone was used to synthesize polyols for polyurethane film formulations. The polyols were synthesized at 140°C using tin(ii) octoate as catalyst, diethanolamine as trifunctional initiator, and with ratios of lactone:initiator of 9:1 or 18:1. Polyol structural features were deduced by comparison of NMR spectral data with those of simple model amide/esters of the initiator. Films were formulated from the renewable polyols, diphenylmethane diisocyanate [or poly(diphenylmethane diisocyanate)], and diethylene glycol. Thermal and mechanical properties of these polyurethane films were measured, demonstrating their potential utility as biobased thermosets for rigid or flexible foams. © 2012 The Royal Society of Chemistry.
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CITATION STYLE
Gurusamy-Thangavelu, S. A., Emond, S. J., Kulshrestha, A., Hillmyer, M. A., MacOsko, C. W., Tolman, W. B., & Hoye, T. R. (2012). Polyurethanes based on renewable polyols from bioderived lactones. Polymer Chemistry, 3(10), 2941–2948. https://doi.org/10.1039/c2py20454a
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