scholarly journals Effects of convection and diffusion of the vapour in evaporating liquid films

2013 ◽  
Vol 732 ◽  
pp. 128-149 ◽  
Author(s):  
Kentaro Kanatani

AbstractWe propose a novel model of a pure liquid film evaporating into an inert gas, taking into account an effect of convection of the vapour by the evaporation flow of the gas. For the liquid phase, the long-wave approximation is applied to the governing equations. Assuming that fluctuations of the vapour concentration in the gas phase are localized in the vicinity of the liquid–gas interface, we consider only the limit of the mass transport equation at the interface. The diffusion term in the vertical direction of the mass transport equation is modelled by introducing the concentration boundary layer above the liquid film and solving the stationary convection–diffusion equation for the concentration inside the boundary layer. We investigate the linear stability of a flat film based on our model. The effect of vapour diffusion along the interface mitigates the Marangoni effect for short-wavelength disturbances. The local variation of vertical advection is found to be negligible. A critical thickness above which the film is stable exists under the presence of gravity. The effect of fluctuation of mass loss of the liquid induced by horizontal vapour diffusion becomes the primary instability mechanism in a very thin region. The effects of the resistance of phase change and the time derivative of the interface concentration are also examined.

2009 ◽  
Author(s):  
Ludovic Dan Lemle ◽  
Tudor Bi^nzar ◽  
Flavius Pater ◽  
Theodore E. Simos ◽  
George Psihoyios ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Abdon Atangana ◽  
Adem Kilicman

The hydrodynamic dispersion equation was generalized using the concept of variational order derivative. The modified equation was numerically solved via the Crank-Nicholson scheme. The stability and convergence of the scheme in this case were presented. The numerical simulations showed that, the modified equation is more reliable in predicting the movement of pollution in the deformable aquifers, than the constant fractional and integer derivatives.


Volume 1 ◽  
2004 ◽  
Author(s):  
Marcelo J. S. de Lemos

This work presents derivations of macroscopic heat and mass transport equations for turbulent flow in permeable structures. Two driving mechanisms are considered to contribute to the overall momentum transport, namely temperature driven and concentration driven mass fluxes. Double-diffusive natural convection mechanism is investigated for the fluid phase in turbulent regime. Equations are presented based on two distinct procedures. The first method considers time averaging of the local instantaneous mass transport equation before the volume average operator is applied. The second methodology employs both averaging operators but in a reverse order. This work is intended to demonstrate that additional transport mechanisms are mathematically derived if temperature, concentration and velocity present simultaneously time fluctuations and spatial deviations within the domain of analysis. A modeled form for the final mass transport equation is presented where turbulent transfer is based on a macroscopic version of the k-ε model.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Ryszard Korycki

AbstractThe cotton-based composite is equipped with a single/double semipermeable membrane made of polyurethane (PU) (100%), which blocks liquid transport to the surrounding environment. The complex problem analyzed involves the coupled transport of water vapor within the textile material, transport of liquid water in capillaries, as well as heat transport with vapor and liquid water. The problem can be described using the mass transport equation for water vapor, heat transport equation, and mass transport equation for liquid moisture, accompanied by the set of corresponding boundary and initial conditions. State variables are determined using a complex multistage solution procedure within the selected points for each layer. The distributions of state variables are determined for different configurations of membranes.


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