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SynopsisThe combination of mixture diagrams and quality functions can be a straightforward and rapid method of simultaneously optimizing polymer formulations for both flame retardancy and smoke suppression. For a semirigid PVC formulation using a three-component additive mixture it was found possible to raise the limiting oxygen index by over 7 units, while simultaneously reducing smoke production by more than 20%. INTRODUCTIONMetal oxides are widely used as either flame retardants (FR) or smoke suppressants (SS) for a wide range of combustible organic polymers. In a recent paper we reported the FR/ SS effects for a range of inorganic and organometallic iron-containing compounds, including iron oxides, incorporated into a flexible PVC formulation.' Antimony and zinc oxides were also studied. Organoiron derivatives were found to possess both FR and SS properties, and ferrocene itself, for example, in a formulation at 1.0 phr (part per hundred of PVC) was found to raise the limiting oxygen index, LOI, by about 3 units while depressing smoke production, as measured by the U.S. National Bureau of Standards (NBS) test, by 28%, whereas the metal oxides studied tended to exhibit either FR or SS properties but not both. Of the iron-containing additives investigated, the oxides were the most effective smoke-suppressants, with an effectiveness similar to the commercial zinc /magnesium oxide preparation Ongard 11, although the LO1 enhancement ( < 2 units) of both these additives is small. On the other hand, antimony (111) oxide is an excellent flame retardant, raising the LO1 by 6.8 units at 5.0 phr, but with substantially increased smoke production ( +40% ). We report here the results of an investigation into the threecomponent additive system, antimony/ iron /zinc oxides, which has used chemometric methods to identify synergic effects and to rapidly develop an optimum formulation for semirigid PVC which has both good SS and good FR properties. Background Theory
SynopsisThe combination of mixture diagrams and quality functions can be a straightforward and rapid method of simultaneously optimizing polymer formulations for both flame retardancy and smoke suppression. For a semirigid PVC formulation using a three-component additive mixture it was found possible to raise the limiting oxygen index by over 7 units, while simultaneously reducing smoke production by more than 20%. INTRODUCTIONMetal oxides are widely used as either flame retardants (FR) or smoke suppressants (SS) for a wide range of combustible organic polymers. In a recent paper we reported the FR/ SS effects for a range of inorganic and organometallic iron-containing compounds, including iron oxides, incorporated into a flexible PVC formulation.' Antimony and zinc oxides were also studied. Organoiron derivatives were found to possess both FR and SS properties, and ferrocene itself, for example, in a formulation at 1.0 phr (part per hundred of PVC) was found to raise the limiting oxygen index, LOI, by about 3 units while depressing smoke production, as measured by the U.S. National Bureau of Standards (NBS) test, by 28%, whereas the metal oxides studied tended to exhibit either FR or SS properties but not both. Of the iron-containing additives investigated, the oxides were the most effective smoke-suppressants, with an effectiveness similar to the commercial zinc /magnesium oxide preparation Ongard 11, although the LO1 enhancement ( < 2 units) of both these additives is small. On the other hand, antimony (111) oxide is an excellent flame retardant, raising the LO1 by 6.8 units at 5.0 phr, but with substantially increased smoke production ( +40% ). We report here the results of an investigation into the threecomponent additive system, antimony/ iron /zinc oxides, which has used chemometric methods to identify synergic effects and to rapidly develop an optimum formulation for semirigid PVC which has both good SS and good FR properties. Background Theory
A 87.5: 12.5 polyester/cotton blended fabric was treated with various concentrations of ammonium sulphate and decabromobiphenyl oxide (DBBO) as well as mixtures of the two additives. The flammability of the resulting systems was determined by the limiting oxygen index (LOI) method and their thermal decomposition by thermogravimetry. Ammonium sulphate was particularly less effective as a flame retardant than the DBBO. Decabromobiphenyl oxide acts in the gas phase to retard the flammability of the polyester while the inorganic salt acts in the condensed phase to decrease that of the cotton. A mechanism for the interaction of ammonium sulphate with cotton was suggested. When a mixture of the two additives containing a high percentage of the bromo-compound was used a significant increase in the LO1 values was observed compared to one having the same total loading but containing a higher percentage of ammonium sulphate. This may be attributed to the stabilizing effect of the released ammonia on the intermediate species formed after the liberation of the bromine radicals from the DBBO.
Polyesteri'cotton blend (87.5: 12.5%) was treated with various concentrations of diammonium hydrogen phosphate (DAP)-Decabromobiphenyl oxide (DBBO) mixture. The flammability of the resulting systems was determined by the limiting oxygen index (LOI) and simultaneous thermal analysis (TA) methods. Evaluation of the results was achieved by plotting the variation of the LO1 with the percentage of ammonium phosphateDBB0 mixtures at constant total additive loadings on triangular diagrams. The activity of the inorganic salt as a flame retardant was found to be synergistically enhanced by the addition of the DBBO. The maximum interaction between the two additives occurred at bromine-phosphorus atomic ratio of about 3: 1. This corresponds to the stoichiometric ratio for the formation of phosphorus tribromide, PBr,, a species which most probably interacts with the acidic products resulting from the thermal decomposition of the polyester and thus changes their nature so that they become no longer capable of recombination with the other decomposition fragments to produce flammable gases.
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