Flame-Retardant Treatment Of Wood With A Diisocyanate and An Oligomer Phosphonate

Authors

  • W. D. Ellis
  • R. M. Rowell

Keywords:

Flame retardant, phosphonate, diisocyanate, pyrolysis, thermogravimetry, thermal degradation

Abstract

An oligomer phosphonate and isophorone diisocyanate, in a chloroform or dichloromethane solution, were impregnated into wood and cured at 105 C. The leach resistance and thermal degradation of treated wood specimens were evaluated. Leaching milled specimens removed up to 49% of the phosphorus and 12% of the nitrogen. The average weight percent gain of solid specimens leached with three 4-day cycles of running water was reduced from 23% to 17% during the first cycle and from 17% to 16% during the second and third cycles. Toluene: ethanol extraction did not remove the reacted chemicals from the wood. Acetone extraction resulted in a 1% to 2% reduction of the weight percent gain values. Thermal analysis showed that the flame-retardant treatment reduced the temperature at maximum rate of pyrolysis approximately 80 C and increased the amount of residual char to about 30%. Leaching raised the temperature on the average 8 C at the maximum rate of pyrolysis and decreased the amount of residual char an average of 3%. The temperature at maximum rate of pyrolysis and amount of residual char indicate the potential effectiveness of this treatment as a leach-resistant, flame-retardant treatment for wood.

References

Browne, F. L., and W. K. Tang. 1962. Thermogravimetric and differential thermal analysis of wood and of wood treated with inorganic salts during pyrolysis. Fire Research Abstract and Review, National Academy of Science, National Research Council 4(1):76-91.nEllis, W. D., and R. M. Rowell. 1984. Reaction of isocyanates with southern pine wood to improve dimensional stability and decay resistance. Wood Fiber Sci. 16(3):349-356.nGoldstein, I. S., and W. A. Dreher. 1961. A non-hygroscopic fire retardant treatment for wood. Forest Prod. J. 11(5):235-237.nJain, R., Kirshan Lal, and H. L. Bhatnagar. 1985. Thermal degradation of cellulose and its phosphorylated products in air and nitrogen. J. Appl. Polym. Sci. 30:897-914.nJuneja, S. C. 1972. Stable and leach-resistant fire-retardants for wood. Forest Prod. J. 22(6): 17-23.nMalz, H., and F. Kassack (Farbenfabriken Bayer A.-G.). 1961. German 1,102,095.nMcKnight, T. S. 1962. The hygroscopicity of wood treated with fire-retardant compounds. Report 190. Forest Research Branch, Canada Department of Forestry.nSchuyten, H. A., J. W. Weaver, and D. J. Reid 1955. Effect of flameproofing agents on cotton cellulose. Ind. Eng. Chem. 47:1433.nShafizadeh, F. 1968. Pyrolysis and combustion of cellulosic materials. Pages 419-470 in Melville L. Wolfrom and R. Stuart Tipson, eds. Adv. Carbohydrate Chem. Vol. 23. Academic Press Inc., New York.nVan Kleeck, A. 1942. Corrosion studies with certain fire-retardant chemicals. Pages 160-171 in Proc. American Wood-Preservers' Association.nVon Bonin, W., and H. Ebneth (Bayer A. -G.). 1987. Ger. Offen. DE 3,528,754.nWillard, J. J., R. Turner, and R. F. Schwenker, Jr. 1965. Chemical structure of resin-treated cellulose. Part I: Trimethylolmelamine-treated cotton. Textile Res. J. 35(6):564-574.n

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Published

2007-06-22

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Research Contributions