To better understand the thermal decomposition and reaction process of a fluorine-containing powdery thermite, PTFE/Al/MnO₂, reactions at different temperatures were investigated by the TG/DSC-MS technique. The corresponding reaction products were characterized with XRD phase analysis. Another three thermite materials, i.e., PTFE/Al, Al/MnO₂, and PTFE/MnO₂, were also prepared for comparison. Results showed that PTFE behaved as both oxidizer and reducer in PTFE/Al/MnO₂ fluorinated thermite. The thermal decomposition and reaction process of as-fabricated ternary thermite could be divided into two stages—the mutual reaction between each of PTFE, Al, and MnO₂ and the subsequent reaction produced between Al and Mn₂O₃/Mn₃O₄/MnF₂. Compared with the three control systems, the specially designed ternary system possessed a shorter reaction time, a faster energy release rate, and a better heat release performance.

When the Al/Ta/PTFE reactive material was sintered at 360 °C in a vacuum sintering furnace, it was found that the material reacted to form a soft fluffy white substance and carbon black. To explore the reaction process further, powder samples of pure PTFE, Al/PTFE, Ta/PTFE and Al/Ta/PTFE, and molded cylindrical specimens were prepared. A TG-DSC test was carried out on the thermal reaction of four reactive materials, and XRD phase analysis was conducted on the white product, formed by the sintering reaction and the residue of the TG-DSC test sample, based on which of the pyrolysis processes and reaction mechanisms were analyzed. The results show that Ta and PTFE could have a chemical reaction at sintering temperature (360 °C) to form soft and fluffy white material TaF₃ and carbon black, which can overflow the surface of the specimen and cause cracking of the specimen, which is tightly pressed. Since no obvious exothermic peak showed up on the TG-DSC curve, the composition of the residue of TG-DSC sample at different temperatures was tested and TaF₃ was detected in the residue at 350 °C and 360 °C, indicating that Ta began to react with PTFE at a temperature range of 340–350 °C. According to the chemical properties and product formation of Ta, it could be speculated that the reaction mechanism between Ta and PTFE involves the PTFE decomposing first, then the fluorine-containing gas product reacting with metal Ta. According to the temperature range of the reaction, it is estimated that PTFE starts to decompose before 500 °C, but it is not detected effectively by TG-DSC, and the introduction of Ta could also affect the decomposition process of PTFE.

To analyze the mechanical properties and reaction characteristics of Al-ZrH₂-PTFE (aluminum-zirconium hydride-polytetrafluoroethylene) composites under quasi-static compression, five types of specimens with different ZrH₂ contents (0%, 5%, 10%, 20% and 30%) were prepared by molding-vacuum sintering. The true stress-strain curves and reaction rates of the different specimens were measured using quasi-static compression. The specific reaction processes were recorded by a high-speed camera. The corresponding reaction products were characterized by the XRD phase analysis, the calorific value was tested by a Calorimeter, and the reaction mechanism was analyzed. According to the results, the strength of the composites increased first and then decreased with the increase in the content of ZrH₂. It reached a maximum of 101.01 MPa at 5%. Violent reaction occurred, and special flames were observed during the reaction of the specimens with 5% ZrH₂. With the increase in the content of ZrH₂, the chemical reaction was hard to induce due to the reduction in strength and toughness of composites. The reaction mechanism of Al/ZrH₂/PTFE reveals that high temperatures at crack tip induced the reaction of Al and PTFE. Subsequently, ZrH₂ decomposed to release hydrogen and generate ZrC. Calorimetric experiment shows that the calorific value of Al/ZrH₂/PTFE with 20% ZrH₂ is higher than that of Al/PTFE. The findings verify the potential of ZrH₂ as an energetic additive for the enhancement of strength and release of the energy of the composites.