Reaction Kinetics of Nitrocellulose Denitration: Model Comparison and Mechanistic Insights

A comprehensive understanding of the denitration kinetics of nitrocellulose-based propellants is crucial for optimizing combustion performance and achieving controllable fabrication. However, most existing studies rely on a single kinetic model, which is restricted by formulation composition and grain geometry, limiting their general applicability. In this work, the denitration rate was quantified using the change in explosion heat, introducing an energy-based characterization approach instead of traditional mass-loss measurements. Three kinetic models (the shrinking-core, pseudo-homogeneous, and Avrami models) were employed to identify the rate-controlling step. The shrinking-core model provided the most accurate description of the process. At moderate reagent concentrations (8 wt.% and 12 wt.%) and temperatures (65–75 °C), denitration was primarily reaction-controlled, while at higher temperatures (80 °C), internal diffusion resistance became significant. The apparent activation energy ranged from 69.8 to 73.7 kJ·mol−1, confirming that chemical reaction is the dominant mechanism. This study refines the kinetic understanding of nitrocellulose denitration and provides theoretical guidance for the controlled fabrication of gradient nitrocellulose propellants with tunable progressive-burning behavior.