Evaluation of self-ignition hazard of bulk materials requires experimental determination of self-ignition temperatures as a function of volume. There are two standardised methods: (1) determination of the self-ignition temperature of dust samples in oven and (2) measurement of the self-ignition temperature of a dust layer deposited on a hot surface. Sometimes, the sample behaviour during these tests makes the second method difficult to apply. The self-ignition phenomena in these two tests rely on the same principles. Their results are interpreted with the help of theoretical relations. The correlation described in this paper can be considered acceptable to deduce self-ignition temperature of a dust layer, based on results of self-ignition of the same dust in heating ovens, if the Biot number (alpha) can be estimated. Uncertainty on the correlation is near 30K. This uncertainty is on the same order of magnitude as the difference in the self-ignition temperature on a hot surface for thickness between 5 and 15 mm.

The flash points of binary mixtures of toluene with two chlorinated hydrocarbons (trichloroethylene and dichloromethane) at different concentrations were investigated to evaluate their predictability by existing mixing rules.Measurements were performed using both open and closed cup flash point testers highlighting complex ignition phenomena. Beyond a certain level of concentration in chlorinated compound, no proper flash is observed, in our test conditions when the flame is presented, but specific behaviors are observed that did not allow the definitive determination of a flash point. The observed phenomena can be attributed to the formation of halogenated radicals, presenting flame-retardant behaviors, by decomposition of the chlorinated vapors at the contact of the flame.Existing mixing rules are based on the consideration of the vapor-liquid equilibrium defining the amount of flammable vapors above the liquid surface. So, the application of such mixing rule failed predicting this specific phenomenon, more likely related to a specific reactivity problem.This work also confirms that the sole consideration of the flash point to investigate the flammability of such mixtures may lead to an underestimation of their actual hazard. Additional experimental tests should be conducted to investigate deeper the flammability of such liquid mixtures.

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