Relationship between the thermal degradation chemistry and flammability of commercial flexible polyurethane foams

Denecker, C. and Liggat, J.J. and Snape, Colin (2006) Relationship between the thermal degradation chemistry and flammability of commercial flexible polyurethane foams. Journal of Applied Polymer Science, 100 (4). pp. 3024-3033. ISSN 0021-8995

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Abstract

In this article, we report the use of a variety of analytical methods, in particular, solid-state 1H-NMR and 13C-NMR to characterize the relationship between the condensed-phase chemistry and burning behavior as determined by a series of combustion tests for two commercially derived flexible polyurethane foams, one combustion-modified. The combustion tests showed that the foams met several regulatory requirements in terms of their fire performance, whether or not they were combustion-modified. Both foams passed the MV SS 302 and CAL 117 small-flame tests. The nonmodified foam failed the Crib 5 test, but this test had a much larger ignition source. The particular problem with the nonmodified foam was melt drip into the flame zone. This led to a steady maintenance of the fuel feed and a rapid escalation of the fire. In contrast, the combustion-modified foam showed little melt drip and self-extinguished. Thermal analysis data for the two foams showed that melamine acted in part as an endothermic heat sink. This alone did not account for the much reduced melt flow and drip of the combustion-modified foam, but the solid-state 1H-NMR data clearly showed that the molecular mobility of the combustion char from combustion-modified foam was lower than the unmodified foam char, which indicated that the flame-retardant formulation in the combustion-modified foam acted by a condensed-phase mechanism.