Filtern
Dokumenttyp
Sprache
- Englisch (12)
- Deutsch (1)
- Mehrsprachig (1)
Schlagworte
- Organic peroxides (14) (entfernen)
Organisationseinheit der BAM
Tests according to the UN Recommendations on the Transport of Dangerous Goods for the determination of explosive properties of organic peroxides have been compared with screening criteria for explosivity based on measurements in a closed mini-autoclave (MCPVT). It will be shown that an additional screening test may be helpful but the information obtained from the UN tests are more important to characterise the specific properties of a substance under different conditions.
Most of the measurements of temperatures in large pool fires are indirect and present a number of complexities due to the interactions of convection, radiation and soot blockage. In the present work these influences for two organic peroxide [tert-butyl peroxybenzoate (TBPB) and tert-butyl peroxy-2-ethylhexanoate (TBPEH)] pool fires are analysed.
Thermocouple measured temperature in the clear flame zone i.e. combustion zone are found to be 250-400 K lower than from the thermographic measurements. The convective and radiative heat flux contributions from the fire on temperature measurements are discussed. CFD (Computational Fluid Dynamics) simulations have been performed for large pool fires and the predicted time averaged flame temperatures were found to be in qualitative agreement with
measurements due to the stoichiometric combustion model used in the present simulations.
Organic peroxides are energetic substances liable to decompose due to exothermic reactions when exposed to uncontrolled temperature, contamination, confinement and quantity. Their safe storage and transportation are the prime concern and chemical industries and regulating authorities. Their accidental release may and most often lead to shape of a pool. In present study, safety distances from such large pool fires (diameter d = 3.4 m) of organic peroxides are numerically predicted by solving the reactive, 3-D time dependent Navier-Stokes equations with reliable assumptions. The present model is validated against the data on buoyant turbulent diffusion flames. The safety distances predicted by simulation assume three regions in a fully developed fire i.e. hot spot, luminous zone and a flame surface. The time averaged data of temperatures of these regions lead to better estimation of irradiances against the measured data. A developed sphere analogy method (for a special class of organic peroxides) for maximum surface emissive power prediction is also verified.
The industrial fire accidents e.g. Buncefield (2005) and Jaipur (2009) have come up with several issues concerning safe storage and transportation of flammable liquids. The pre and post fire consequences are therefore important to be analyzed prior to the handling of flammable fuels. Pool or/and tank fire is the most often seen scenario after the leak/spill of liquid fuel. An overview of the typical scenarios from large hydrocarbon and organic peroxide pool fires and their respective safety distances for the people and the infrastructure are the important subjects of this paper.
The mass burning rate of pool fires of organic peroxides do not vary appreciably with the pool size as have been observed for the hydrocarbons. Instead the decomposition temperature largely controls the same. The dependence of mass burning rate on the decomposition temperatures namely self-accelerating decomposition temperature (SADT) and extrapolated onset temperature measured by differential scanning calorimetry (DSC) for organic peroxide pool fires are identified and correlations are developed.
We present a prediction (estimation, calculation, screening) method for the estimation of the self-accelerating decomposition temperature (SADT) for liquid organic peroxides from differential scanning calorimetry (DSC) measurements based on the concepts of thermal explosion theory originally introduced by Semonov which are adopted to our problem assuming nth-order reaction kinetics. For the peroxides under investigation, we demonstrate good agreement with the experimental SADT. This method can be used as a quick and easy applicable method for the estimation of the critical temperatures.