An Accurate Experimental Method for Determining the Injectant Mass Fraction Distribution in a Supersonic Turbulent Flow Mixing Region

Author(s):  
Alexander Gonor ◽  
Vitali Khaikine ◽  
James Gottlieb ◽  
Isaiah Blankson
1997 ◽  
Vol 336 ◽  
pp. 379-409 ◽  
Author(s):  
PEDRO L. GARCÍA-YBARRA ◽  
JOSE L. CASTILLO

The concentration distribution of massive dilute species (e.g. aerosols, heavy vapours, etc.) carried in a gas stream in non-isothermal boundary layers is studied in the large-Schmidt-number limit, Sc[Gt ]1, including the cross-mass-transport by thermal diffusion (Ludwig–Soret effect). In self-similar laminar boundary layers, the mass fraction distribution of the dilute species is governed by a second-order ordinary differential equation whose solution becomes a singular perturbation problem when Sc[Gt ]1. Depending on the sign of the temperature gradient, the solutions exhibit different qualitative behaviour. First, when the thermal diffusion transport is directed toward the wall, the boundary layer can be divided into two separated regions: an outer region characterized by the cooperation of advection and thermal diffusion and an inner region in the vicinity of the wall, where Brownian diffusion accommodates the mass fraction to the value required by the boundary condition at the wall. Secondly, when the thermal diffusion transport is directed away from the wall, thus competing with the advective transport, both effects balance each other at some intermediate value of the similarity variable and a thin intermediate diffusive layer separating two outer regions should be considered around this location. The character of the outer solutions changes sharply across this thin layer, which corresponds to a second-order regular turning point of the differential mass transport equation. In the outer zone from the inner layer down to the wall, exponentially small terms must be considered to account for the diffusive leakage of the massive species. In the inner zone, the equation is solved in terms of the Whittaker function and the whole mass fraction distribution is determined by matching with the outer solutions. The distinguished limit of Brownian diffusion with a weak thermal diffusion is also analysed and shown to match the two cases mentioned above.


Author(s):  
Peng Zhang ◽  
Yu Rao ◽  
Yanlin Li

This paper presents a numerical study on turbulent flow and heat transfer in the channels with a novel hybrid cooling structure with miniature V-shaped ribs and dimples on one wall. The heat transfer characteristics, pressure loss and turbulent flow structures in the channels with the rib-dimples with three different rib heights of 0.6 mm, 1.0 mm and 1.5 mm are obtained for the Reynolds numbers ranging from 18,700 to 60,000 by numerical simulations, which are also compared with counterpart of a pure dimpled and pure V ribbed channel. The results show that the overall Nusselt numbers of the V rib-dimple channel with the rib height of 1.5 mm is up to 70% higher than that of the channels with pure dimples. The numerical simulations show that the arrangement of the miniature V rib upstream each dimple induces complex secondary flow near the wall and generates downwashing vortices, which intensifies the flow mixing and turbulent kinetic energy in the dimple, resulting in significant improvement in heat transfer enhancement and uniformness.


Processes ◽  
2018 ◽  
Vol 6 (8) ◽  
pp. 119 ◽  
Author(s):  
Zhanwei Wang ◽  
Kun Liu ◽  
Jiuxin Ning ◽  
Shulei Chen ◽  
Ming Hao ◽  
...  

Microdroplet dosing to cell on a chip could meet the demand of narrow diffusion distance, controllable pulse dosing and less impact to cells. In this work, we studied the diffusion process of microdroplet cell pulse dosing in the three-layer sandwich structure of PDMS (polydimethylsiloxane)/PCTE (polycarbonate) microporous membrane/PDMS chip. The mathematical model is established to solve the diffusion process and the process of rhodamine transfer to micro-traps is simulated. The rhodamine mass fraction distribution, pressure field and velocity field around the microdroplet and cell surfaces are analyzed for further study of interdiffusion and convective diffusion effect. The cell pulse dosing time and drug delivery efficiency could be controlled by adjusting microdroplet and culture solution velocity without impairing cells at micro-traps. Furthermore, the accuracy and controllability of the cell dosing pulse time and maximum drug mass fraction on cell surfaces are achieved and the drug effect on cells could be analyzed more precisely especially for neuron cell dosing.


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