Linear instability of Poiseuille flows with highly non-ideal fluids

被引:21
作者
Ren, Jie [1 ]
Fu, Song [2 ]
Pecnik, Rene [1 ]
机构
[1] Delft Univ Technol, Proc & Energy Dept, Leeghwaterstr 39, NL-2628 CB Delft, Netherlands
[2] Tsinghua Univ, Sch Aerosp Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
complex fluids; compressible flows; instability; DIRECT NUMERICAL-SIMULATION; BOUNDARY-LAYER; BULK VISCOSITY; CHANNEL FLOW; STABILITY; TRANSITION; TURBULENCE; STATE;
D O I
10.1017/jfm.2018.815
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
The objective of this work is to investigate linear modal and algebraic instability in Poiseuille flows with fluids close to their vapour-liquid critical point. Close to this critical point, the ideal gas assumption does not hold and large non-ideal fluid behaviours occur. As a representative non-ideal fluid, we consider supercritical carbon dioxide (CO2) at a pressure of 80 bar, which is above its critical pressure of 73.9 bar. The Poiseuille flow is characterized by the Reynolds number (Re = p(w)(*)u(r)(*)h(*) / mu(*)(w)), the product of the Prandtl (Pr = mu C-*(w)pw(*)/K-w(*)) and Eckert numbers (Ec = u(r)(*2)/(CpwTw*)-T-*) and the wall temperature that in addition to pressure determine the thermodynamic reference condition. For low Eckert numbers, the flow is essentially isothermal and no difference with the well-known stability behaviour of incompressible flows is observed. However, if the Eckert number increases, the viscous heating causes gradients of thermodynamic and transport properties, and non-ideal gas effects become significant. Three regimes of the laminar base flow can be considered: the subcritical (temperature in the channel is entirely below its pseudo-critical value), transcritical and supercritical temperature regimes. If compared to the linear stability of an ideal gas Poiseuille flow, we show that the base flow is modally more unstable in the subcritical regime, inviscid unstable in the transcritical regime and significantly more stable in the supercritical regime. Following the principle of corresponding states, we expect that qualitatively similar results will be obtained for other fluids at equivalent thermodynamic states.
引用
收藏
页码:89 / 125
页数:37
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