Curing and Cross-Linking Processes in the Poly(3,3-bis-azidomethyl oxetane)-tetrahydrofuran/Toluene Diisocyanate/Trimethylolpropane System: A Density Functional Theory and Accelerated ReaxFF Molecular Dynamics Investigation.

The physical and chemical properties of solid propellant are influenced by the composition and structure of the binder, with its network structure being formed through curing and cross-linking reactions. Therefore, understanding the mechanisms of these reactions is crucial. In this study, we investigated the curing and cross-linking mechanisms of poly(3,3-bis-azidomethyl oxetane)-tetrahydrofuran (PBT), toluene diisocyanate (TDI), and trimethylolpropane (TMP) using a combination of density functional theory (DFT) calculations and accelerated ReaxFF molecular dynamics (MD) simulations. DFT calculations revealed that the steric effect of the -CH group in TDI exerts a significant influence on the curing reaction between TDI and PBT. Additionally, in the cross-linking process, the energy barrier for TDI reacting with TMP was found to be much lower than that for TDI reacting with the PBT-TDI intermediate. Subsequently, we conducted competing reaction processes of TMP/TDI-PBT-TDI cross-linking and TDI-PBT-TDI self-cross-linking using accelerated MD simulations within the fitted ReaxFF framework. The results showed that the successful frequency of TMP/TDI-PBT-TDI cross-linking was substantially higher than that of TDI-PBT-TDI self-cross-linking, consistent with the energy barrier results from DFT calculations. These findings deepen our understanding of the curing and cross-linking mechanisms of the PBT system, providing valuable insights for the optimization and design of solid propellants.