Abstract

Strained polycyclic hydrocarbons are one of the most important classes of high-energy density fuels. In this work, the thermodynamics and initial pyrolysis kinetics of five strained polycyclic hydrocarbons, which are isomers of JP-10 and are linearly aggregates of two cyclopropyl rings and one cyclobutyl ring, were investigated using quantum chemical computations. The initial pyrolysis reactions include ring bond breaking and bridge bond breaking. The ring bond breaking reactions include a diradical pathway which is the direct C-C bond breaking to produce a diradical and an isomerization pathway involving concert bond breaking and H-atom transfer, and the bridge bond breaking reactions lead to two radicals. Our potential energy calculation shows that the ring bond breaking reactions are much more energetically favorable than the bridge bond breaking reactions, which can be neglected in the initial pyrolysis process of strained polycyclic hydrocarbons. The rate constants of the ring bond breaking reactions were computed using variational transition state theory (VTST) or transition state theory (TST). Our calculated results demonstrated that ring bond breaking reactions of the three-membered ring are competitive with that of the four-membered ring. The studied reactions are divided into classes depending on the size of the rings (three- or four-membered ring) and the types of the carbon atoms of the breaking C-C bond (Cs-Cs, Cs-Ct, Ct-Ct and Cq-Cs). Reaction rate rules are established for each class, which are useful for the mechanism generation for analogous strained polycyclic hydrocarbons. Thermodynamic properties including net calorific values per mole, gravimetric net heat of combustion and impulse time of our studied strained polycyclic hydrocarbons are higher than those of JP-10. A comparison of the initial pyrolysis kinetics of our studied strained polycyclic hydrocarbons with the isomer JP-10 indicates that these compounds may be easier to pyrolyze.

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