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作 者:WANG XingJian LAFON Patrick SUNDARAM Dilip YANG Vigor
机构地区:[1]Department of Mechanical and Civil Engineering,Florida Institute of Technology,Melbourne,Florida 32901,USA [2]Department of Mechanical and Nuclear Engineering,The Pennsylvania State University,University Park,PA 16802,USA [3]School of Aerospace Engineering,Georgia Institute of Technology,Atlanta,GA 30332,USA
出 处:《Science China(Technological Sciences)》2020年第12期2649-2656,共8页中国科学(技术科学英文版)
摘 要:Liquid vaporization under thermodynamic phase non-equilibrium condition at the gas-liquid interface is investigated over a wide range of fluid state typical of many liquid-fueled energy conversion systems. The validity of the phase-equilibrium assumption commonly used in the existing study of liquid vaporization is examined using molecular dynamics theories. The interfacial mass flow rates on both sides of the liquid surface are compared to the net vaporization rate through an order-of-magnitude analysis.Results indicated that the phase-equilibrium assumption holds valid at relatively high pressures and low temperatures,and for droplets with relatively large initial diameters(for example,larger than 10 μm for vaporizing oxygen droplets in gaseous hydrogen in the pressure range from 10 atm to the oxygen critical state). Droplet vaporization under superheated conditions is also explored using classical binary homogeneous nucleation theory,in conjunction with a real-fluid equation of state. It is found that the bubble nucleation rate is very sensitive to changes in saturation ratio and pressure;it increases by several orders of magnitude when either the saturation ratio or the pressure is slightly increased. The kinetic limit of saturation ratio decreases with increasing pressure,leading to reduced difference between saturation and superheat conditions. As a result,the influence of nonequilibrium conditions on droplet vaporization is lower at a higher pressure.
关 键 词:liquid vaporization droplet vaporization superheated vaporization thermodynamic phase equilibrium thermodynamic phase non-equilibrium vapor nucleation
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