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Reactive materials (RMs) are special type of impact-initiated energetic materials that have been widely studied with broad military application prospects. However, simulating the ignition and reaction of RMs using current numerical methods is difficult due to their complex mechanism related to high dynamic loads. In this work, based on a theoretical model consisting of impact ignition criteria and chemical reaction rate of polymer-based RMs, a numerical method with a unified equation of state was proposed and compiled as an executable program. Experiments consisting of typical polytetrafluoroethylene /Al RM projectiles impacting double-spaced plates were conducted and simulated using the user-compiled program, and the results verified the effectiveness of the numerical method. The simulation also qualitatively analyzed the second-collision induced reaction enhancement mechanism. In addition, the results revealed that the kinetic-chemical combined effect is a crucial factor that determined the damage enhancement effect on the rear plates. [ABSTRACT FROM AUTHOR]

In order to study the microscopic reaction mechanism and kinetic model of Al/PTFE, a reactive force field (ReaxFF) was used to simulate the interface model of the Al/PTFE system with different oxide layer thicknesses (0 Å, 5 Å, 10 Å), and the thermochemical behavior of Al/PTFE at different heating rates was analyzed by simultaneous thermal analysis (TG-DSC). The results show that the thickness of the oxide layer has a significant effect on the reaction process of Al/PTFE. In the system with an oxide layer thickness of 5 Å, the compactness of the oxide layer changes due to thermal rearrangement, resulting in the diffusion of reactants (fluorine-containing substances) through the oxide layer into the Al core. The reaction mainly occurs between the oxide layer and the Al core. For the 10 Å oxide layer, the reaction only exists outside the interface of the oxide layer. With the movement of the oxygen ions in the oxide layer and the Al atoms in the Al core, the oxide layer moves to the Al core, which makes the reaction continue. By analyzing the reaction process of Al/PTFE, the mechanism function of Al/PTFE was obtained by combining the shrinkage volume model (R3 model) and the three-dimensional diffusion (D3 model). In addition, the activation energy of Al/PTFE was 258.8 kJ/mol and the pre-exponential factor was 2.495 × 1015 min−1. The research results have important theoretical significance and reference value for the in-depth understanding of the microscopic chemical reaction mechanism and the quantitative study of macroscopic energy release of Al/PTFE reactive materials. [ABSTRACT FROM AUTHOR]

The chemical reaction mechanism of Ni/Al composites, referring to the exothermic mechanism and intermetallic-forming mechanism, is investigated by using molecular dynamics simulation. During the exothermic process, the influences of Ni/Al atomic ratios and crystallographic orientations on the exothermic reaction are systematically investigated. The exothermic mechanism can be explained by the atomic diffusion that increases the quantity of Ni–Al chemical bonds. There are two pathways to form the intermetallic phase during the chemical reaction. One is the atomic diffusion that forms the B2 NiAl phase at the interface. The other way is quenching the sample to the room temperature, but the type of intermetallic phases depends on the Ni/Al atomic ratio and ignition temperature. [ABSTRACT FROM AUTHOR]

In order to study the morphology characteristics of the PTFE/Al reactive shaped charge jet and the chemical reaction during the jet formation, PTFE/Al reactive liners with aluminum particle sizes of 5 μm and 100 μm were prepared. The parameters of the Johnson–Cook constitutive model of PTFE/Al reactive materials (RMs) were obtained through quasi-static compression experiments and SHPB (Split Hopkinson Pressure Bar) experiments. X-ray imaging technology was used to photograph the shape of reactive shaped charges jet at two different time points. The AUTODYN secondary development technology was used to simulate the jet formation, and the simulation results are compared with the experimental results. The results show that the simulation results are close to the experimental results, and the error is in the range of 4–8%. Through analysis, it is observed that the RMs reacted during the PTFE/Al reactive shaped charge jet formation, and due to the convergence of the inner layer of the liner during the jet formation, the chemical reaction of the jet is from inside to outside. Secondly, the particle size of aluminum powder has an influence on the chemical reaction and morphology of the jet. During the jet formation, there were fewer RMs reacted when the PTFE/Al reactive liners were prepared with 100 μm aluminum powder. Compared with 5 μm aluminum powder, when the aluminum powder is 100 μm, the morphology of the jet is more condensed, which is conducive to generating greater penetration depth. [ABSTRACT FROM AUTHOR]

Reactive material (RM) is a special kind of energetic material that can react and release chemical energy under highly dynamic loads. However, its energy release behavior is limited by its own strength, showing unique unsustainable characteristics, which lack a theoretical description. In this paper, an impact-initiated chemical reaction model is proposed to describe the ignition and energy release behavior of Al/PTFE RM. The hotspot formation mechanism of pore collapse was first introduced to describe the decomposition process of PTFE. Material fragmentation and PTFE decomposition were used as ignition criteria. Then the reaction rate of the decomposition product with aluminum was calculated according to the gas-solid chemical reaction model. Finally, the reaction states of RM calculated by the model are compared and qualitatively consistent with the experimental results. The model provides insight into the thermal-mechanical-chemical responses and references for the numerical simulation of impact ignition and energy release behavior of RM. [ABSTRACT FROM AUTHOR]

In recent years, polytetrafluoroethylene (PTFE)/aluminum (Al) energetic materials with high-energy density have attracted extensive attention and have broad application prospects, but the low-energy release efficiency restricts their application. In this paper, oxide, bismuth trioxide (Bi2O3) or molybdenum trioxide (MoO3) are introduced into PTFE/Al to improve the chemical reaction performance of energetic materials. The pressurization characteristics of PTFE/Al/oxide as pressure generators are compared and analyzed. The experiments show that the significantly optimized quasi-static pressure peak, impulse, and energy release efficiency (0.162 MPa, 10.177 s·kPa, and 0.74) are achieved for PTFE/Al by adding 30 wt.% Bi2O3. On the other hand, the optimal parameter obtained by adding 10% MoO3 is 0.147 MPa, 9.184 s·kPa, and 0.68. Further, the mechanism of enhancing the energy release performance of PTFE/Al through oxide is revealed. The mechanism analysis shows that the shock-induced energy release performance of PTFE/Al energetic material is affected by the intensity of the shock wave and the chemical reaction extent of the material under the corresponding intensity. The oxide to PTFE/Al increases the intensity of the shock wave in the material, but the chemical reaction extent of the material decreases under the corresponding intensity. [ABSTRACT FROM AUTHOR]

Reactive material fragment is an extremely efficient damage enhancement technology that incorporates the defeat mechanisms of kinetic energy and chemical energy. In this paper, the polymer-based reactive material fragment/target interactions are investigated. Related dynamic testing techniques for energy release characteristics of reactive material fragments are presented, and a series of ballistic experiments is conducted. The results show the reactive material fragment, which perforates the closed test chamber, undergoes a violent chemical reaction under highly dynamic loads and releases great amounts of thermo-chemical energy on the interior. The impact-initiated process and energy release behavior are markedly influenced by the impact velocity, indicating the material's fracture is of importance to the reaction. A relationship between the maximum pressure inside the chamber and the reaction efficiency is derived to analyze the influence quantitatively, and the venting effects are also considered. [ABSTRACT FROM AUTHOR]

The traditional polytetrafluoroethylene (PTFE)/Al reactive material liner shaped charge generally produces insufficient penetration depth, although it enlarges the penetration hole diameter by chemical energy release inside the penetration crater. As such, a novel high-density reactive material liner based on the PTFE matrix was fabricated, and the corresponding penetration performance was investigated. Firstly, the PTFE/W/Cu/Pb high-density reactive material liner was fabricated via a cold pressing/sintering process. Then, jet formation and penetration behaviors at different standoffs were studied by pulse X-ray and static experiments, respectively. The X-ray results showed that the PTFE/W/Cu/Pb high-density reactive material liner forms an excellent reactive jet penetrator, and the static experimental results demonstrated that the penetration depth of this high-density reactive jet increased firstly and then decreased by increasing the standoff. When the standoff was 1.5 CD (charge diameter), the penetration depth of this reactive jet reached 2.82 CD, which was significantly higher than that of the traditional PTFE/Al reactive jet. Moreover, compared with the conventional metal copper jet penetrating steel plates, the entrance hole diameter caused by this high-density reactive jet improved 29.2% at the same standoff. Lastly, the chemical reaction characteristics of PTFE/W/Cu/Pb reactive materials were analyzed, and a semi-empirical penetration model of the high-density reactive jet was established based on the quasi-steady ideal incompressible fluid dynamics theory. [ABSTRACT FROM AUTHOR]