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Induction period in the low‐temperature thermal oxidation of saturated hydrocarbons: Example of polyethylene
Author(s) -
Richaud Emmanuel,
Colin Xavier,
Fayolle Bruno,
Audouin Ludmila,
Verdu Jacques
Publication year - 2008
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.20347
Subject(s) - chemistry , radical , induction period , decomposition , kinetics , thermal decomposition , hydrocarbon , photochemistry , reaction rate constant , substrate (aquarium) , oxygen , kinetic scheme , thermal , organic chemistry , thermodynamics , catalysis , physics , oceanography , quantum mechanics , geology
Thermal oxidation of hydrocarbon substrates at low‐to‐moderate temperature, typically T ≤ 150 ° C, results from a radical chain process initiated by hydroperoxide decomposition and displays an induction period. A reliable model exists to simulate oxidation kinetics, but an incertitude remains on initial steps because they are out of reach of all available analytical methods. This work is aimed to have a kinetic approach of the problem, by comparing various mechanisms, i.e., (A) bimolecular decomposition of initially present hydroperoxides; (B) combined uni‐ and bimolecular decomposition of hydroperoxides; (C) the presence of radicals at the beginning of the exposure; and (D) radicals generation at (low) constant rate from irradiation, for instance by ionizing radiation linked to natural radioactivity or from a direct oxygen–substrate reaction. Scheme A is not realistic at low initial hydroperoxide concentrations. All the other mechanisms generate similar behaviors: the induction time tends toward a constant value almost independent of the nature of initial steps, when the concentration of precursors (initially present hydroperoxides or radicals) or the rate of their initial production (from species other than hydroperoxides) tends toward zero. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 40: 769–777, 2008