Fe-BTC effectively enhances the thermal decomposition of AP and improves the combustion properties of BAMO–THF propellant with AP as the oxidizer.

No abstract

A novel catalyst CoFe2O4/RGO has been synthesized and shows enhanced catalytic activity on thermal decomposition of ammonium perchlorate.

As a new type of carbon material, graphene oxide aerogel (GA) is widely used in catalysis due to its porous structure, high-efficiency adsorption, and superb conductivity. In this study, GA was prepared into a dense coating layer surrounding ZnCo 2 O 4 /ZnO particles to form a composite GA-ZnCo 2 O 4 / ZnO by means of a hydrothermal, blast drying, and vacuum-freezedrying approach applied to catalyze the thermal decomposition of ammonium perchlorate (AP). The physicochemical properties of the obtained GA-ZnCo 2 O 4 /ZnO were characterized by different analytical methods. Scanning electron microscopy (SEM) analysis exhibited that GA is coated on the surface of ZnCo 2 O 4 /ZnO, forming a dense layer. Brunner Emmet Teller (BET) measurement results show that GA-ZnCo 2 O 4 /ZnO has a smooth macropore distribution curve and a larger specific surface area. Moreover, The catalytic effect investigation on AP with GA-ZnCo 2 O 4 /ZnO: the high temperature decomposition (HTD) peak temperature of AP in the presence of 5 wt % GA-ZnCo 2 O 4 /ZnO was reduced from 441 to 294 °C, and the exotherm of AP was expanded from 205 to 1275 J/g at a heating rate of 15 °C/min. Through the calculation, GA-ZnCo 2 O 4 /ZnO makes the activation energy and Gibbs free energy of the AP pyrolysis lower so that the reaction is easier to occur. Thermogravimetric−mass (TG−MS) spectrometry revealed that during thermal decomposition of AP, GA-ZnCo 2 O 4 /ZnO leveraged the synergistic catalysis of ZnCo 2 O 4 /ZnO and GA that boosted the flow of electrons from ClO 4 − to O 2 and increased the absorption of the gas product to accelerate the AP pyrolysis. These results provided a facile strategy to prepare GA-based composite catalysts with extraordinary application prospects in the domain of solid propellants.

Metal hydrides are regarded as a series of promising hydrogen-supplying fuel for solid rocket propellants. Their effects on the energetic and combustion performances of propellants are closely related to their reaction mechanisms. Here we report a first attempt to determine the reaction mechanism of ZrH, a high-density metal hydride, in the combustion of a double-base propellant to evaluate its potential as a fuel. ZrH is determined to possess good resistance to oxidation by nitrocellulose and nitroglycerine. Thus its combustion starts with dehydrogenation to generate H and metallic Zr. Subsequently, the newly formed Zr and H participate in the combustion and, especially, Zr melts and then combusts on the burning surface which favors the heat feedback to the propellant. This phenomenon is completely different from the combustion behavior of the traditional fuel Al, where the Al particles are ejected off the burning surface of the propellant to get into the luminous flame zone to burn. The findings in this work validate the potential of ZrH as a hydrogen-supplying fuel for double-base propellants.