Molecular Dynamics Simulations of the Thermal Decomposition of RDX/HTPB Explosives.

Abstract

The addition of binders to energetic materials is known to complicate the thermal decomposition process of such materials. To assess this effect, the present work studied the thermal decomposition of cyclotrimethylene trinitramine (RDX)/hydroxy-terminated polybutadiene (HTPB) mixtures and of pure RDX over the temperature range of 2000-3500 K by combining the classical reaction and first-principles molecular dynamics methods. The incorporation of HTPB as a binder was found to significantly reduce the decomposition rate of RDX. At 3500 K, the decay rate constant of RDX in the RDX/HTPB system is 2.0141 × 1012 s-1, while it is 2.7723 × 1012 s-1 in the pure RDX system. However, the binder HTPB had little effect on the initial decomposition mechanism, which involved the rupture of N-NO2 bonds to produce NO2. The HTPB was predicted to undergo dehydrogenation and chain breaking. The free H resulting from these processes was predicted to react with low-molecular-weight intermediates generated by the RDX, resulting in greater equilibrium quantities of the final products H2O and H2 being obtained from the mixed system compared with pure RDX. HTPB-chain fragments were also found to combine with the primary RDX decomposition product NO2 to inhibit the formation of N2 and CO2.