Abstract
Several toluene diisocyanates blocked with various substituted phenols were prepared. They were characterized by elemental analysis, infra-red and 1H nuclear magnetic resonance spectroscopy. The deblocking temperatures were determined by use of infra-red spectroscopy and by carbon dioxide evolution methods. The thermal stability of the blocked isocyanate was less for the ortho-substituted phenols than for the para isomers. Dissociation temperatures were also reduced by electron-withdrawing groups. The dissolution temperatures of the adducts were determined in propylene glycol, poly(ethylene glycol) 400 and hydroxyl-terminated poly(butadiene). © 1993.
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Kothandaraman, H., & Nasar, A. S. (1993). The thermal dissociation of phenol-blocked toluene diisocyanate crosslinkers. Polymer, 34(3), 610–615. https://doi.org/10.1016/0032-3861(93)90558-R
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