Small scale pool fires: The case of toluene

Abstract

Industrial applications adopting toluene as a solvent have been largely extended in recent years, including solutions within the framework of the energy transition and energy storage technologies. The potential use of this flammable compound in a different set of operative conditions and compositions requires a comprehensive and complete knowledge of its fire behaviour and combustion kinetic. To this scope, an innovative experimental procedure applicable to liquid reactive systems was developed for this scope and implemented at different boundary conditions. More specifically, the specimen was exposed to air and heat fluxes between 7 and 50 kW/m², at a constant sample surface of 0.01 m², an initial sample thickness of 0.01 m, and a distance between the sample and the horizontally oriented conical-shaped heater of 0.025 m. Measurements were compared with data from the current literature, when available, demonstrating the robustness and validity of the adopted procedure. Although an increase in the external flux leads to growing mass burning rates (i.e., from 0.47 g/s to 0.85 g/s), negligible effects on the ignitability were observed. Conversely, a peak in the heat release rate at 35 kW/m² was measured. The observed reduction at higher external heat fluxes was attributed to less effective combustion, demonstrating that the maximum expected heat flux cannot be considered as an aprioristic worst-case scenario for the evaluation of pool fires. The collected data were, then, further utilized to obtain insights on the formation of the main products, including soot tendency. Based on the collected data a simplified kinetic model suitable for the computational fluid dynamics was proposed to reproduce the chemistry of the system.