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B. Roduit1*, M. Hartmann1, S. Kaneko2, P. Folly3, P. Brodard4, S- Gomez4, R. Marti4, J.-N. Aebischer4

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1AKTS AG, TECHNOArk 1, 3960 Siders, Switzerland, http://www.akts.com
2Palmetrics Corp., 350-1328, Hirose-dai 2-16-15, Sayama city, Japan
3armasuisse, Science and Technology Centre, 3602 Thun, Switzerland
4University of Applied Sciences of Western Switzerland, Bd de Pérolles 80, 1705 Fribourg, Switzerland
* Author to whom correspondence should be addressed

Abstract

The runaway reactions are generally investigated by the time-consuming Accelerating Rate Calorimetry (ARC) or in isothermal (ISO-ARC) or heat-waitsearch (HWS) modes. In present poster we discuss the application of the Differential Scanning Calorimetry (DSC) for the determination of the Time to Maximum Rate under adiabatic conditions (TMRad) of various concentrations of Ditert- butyl peroxide (DTBP) in toluene. Additionally we present the method of simulation of the course of ARC experiments. We propose an advanced elaboration of the DSC data leading to the determination of the kinetic parameters of investigated reactions which, in turn, allows the simulation of the reaction course under any temperature mode. These kinetic parameters obtained in mg-scale considered simultaneously with a heat balance give a powerful tool for the prediction of the thermal behaviour of the substance in kg-scale (pseudo-adiabatic conditions: SADT, cook-off) or in ton-scale (adiabatic conditions: TMRad).