Understanding the dynamic characteristic of the cavitation bubble near a solid wall is a fundamental issue for the bubble collapse application and prevention. In the present work, an improved three-dimensional multi-relaxation-time pseudopotential lattice Boltzmann model is adopted to investigate the cavitation bubble collapse near the solid wall. With respect to thermodynamic consistency, Laplace law verification, the three-dimensional pseudopotential multi-relaxation-time lattice Boltzmann model is investigated. By the theoretical analysis, it is proved that the model can be regarded as a solver of the Rayleigh–Plesset equation, and confirmed by comparing the results of the lattice Boltzmann simulation and the Rayleigh–Plesset equation calculation for the case of cavitation bubble collapse in the infinite medium field. The bubble collapse near the solid wall is modeled using the improved pseudopotential multi-relaxation-time lattice Boltzmann model. We find the lattice Boltzmann simulation and the experimental results have the same dynamic process by comparing the bubble profiles evolution. Form the pressure field and the velocity field evolution it is found that the tapered higher pressure region formed near the top of the bubble is a crucial driving force inducing the bubble collapse. This exploratory research demonstrates that the lattice Boltzmann method is an alternative tool for the study of the interaction between collapsing cavitation bubble and matter.
Fuel vapor concentration is a key parameter for assessing the flammability of aircraft fuel tanks. However, the current research on RP-3 (Rocket Propellant-3) fuel vapor concentration is inadequate. This study categorizes fuel components by the number of carbon atoms and utilizes Raoult’s law to estimate the gas–liquid equilibrium relationship of each constituent element under equilibrium conditions. The equilibrium-state model is experimentally validated, and the differences in the constituents and fuel vapor concentrations of RP-3 and Jet-A (Jet Fuel-A) fuels are analyzed. In addition, an empirical correlation between the overall hydrocarbon concentration of RP-3 fuel vapor and the temperature and pressure in the equilibrium state is established, providing a theoretical basis for determining RP-3 fuel vapor concentration in related investigations. Furthermore, a transient prediction model of fuel vapor concentration is developed using the lumped parameter approach that considers the heat exchange among the fuel, gas, wall, and environment. The model’s accuracy is confirmed by comparing it to existing literature. Then, the temperature and fuel vapor concentration variation patterns in the fuel tank are calculated and evaluated under two typical flight scenarios. The results show a significant difference between the calculated fuel vapor concentration values obtained through equilibrium-state and transient models. Therefore, in the design of fuel vapor catalytic inerting systems, it is crucial to consider both the equilibrium and transient fuel vapor concentration values rather than relying solely on the former. Throughout the flight envelope, gas phase and fuel phase temperatures in RP-3, Jet-A, and C10H22 fuel tanks exhibit minimal differences. However, significant variations in fuel vapor concentration exist depending on the flight state and envelope. Hence, regarding RP-3 as equivalent to C10H22 is inappropriate. Additionally, fuel vapor concentration is a more suitable metric than fuel temperature for assessing fuel tank flammability.
To investigate the parameters of sucrose dust explosion, the minimum ignition energy (MIE) and minimum ignition temperature (MIT) were evaluated. The experiments tested the MIE of sucrose dust under different conditions of dust quantity, ignition delay time (IDT), and powder injection pressure (PIP). The experiments tested the MIT of different particle sizes. The results demonstrate that the MIE of sucrose powder under three conditions was an open-up quadratic polynomial. When the dust quantity, the IDT, and PIP were 0.5 g (417 g/m3), 90 ms, and 150 kPa, respectively, the MIE was 58.9 mJ, 62.6 mJ, and 52.4 mJ. The MIT was positively correlated with the particle size of sucrose dust, and the MIT was 340 °C. At the molecular level, the “O–H” bonds of the sucrose molecule hydroxyl groups were broken by the discharge of electrodes or high temperature to generate H2. The combustion of H2 caused the explosion to spread to the surrounding sucrose dust and made the deposited dust rise, forming an interlocking explosion. The explosion would not stop until the dust concentration dropped below the lowest explosion limit. The results of this study can provide guidance for sucrose enterprises to prevent dust explosion accidents.
In order to investigate the explosion mechanism of sucrose in the air atmosphere, the explosion intensity under different ignition delay times (IDT), powder input pressures (PIP), and concentrations were studied using a 20L-sphere. The sucrose particles were analyzed in a synchronized thermal analyzer (STA) and scanning electron microscope (SEM). The results are as follows: 1. The DSC curve has two endothermic peaks and one exothermic peak, respectively at T = 180.5 ℃, 510.2 ℃ and 582.6 ℃. 2. The explosion intensity varies with the experiment conditions. The maximum explosion pressure (Pmax) appears when IDT = 90 ms, PIP = 1.5 MPa and concentration = 625 g/m3. 3. The explosive mechanism is a homogeneous combustion mechanism based on particle surface pyrolysis and volatilization. Because of the decomposition, H2, CO, furfural, and other flammable gas-phase products are released, then surface burn appears, which leads to the crystal rupture on account of thermal imbalance, resulting in multiple flame points and a chain explosion. As the temperature of the 20L-sphere rises, more explosive products are released, which causes a rapidly expanding explosion and eventually forms the explosion. This paper can be used as a reference for the prevention of explosion accidents in sucrose production processing.
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