The Effect of Shear Flow and Dissolved Gas Diffusion on the Cavitation in a Submerged Journal Bearing

2000 ◽  
Vol 123 (3) ◽  
pp. 494-500 ◽  
Author(s):  
M. Groper ◽  
I. Etsion

Two possible, long standing speculated mechanisms are theoretically investigated in an attempt to understand previous experimental observations of pressure build up in the cavitation zone of a submerged journal bearing. These mechanisms are (1) the shear of the cavity gas bubble by a thin lubricant film dragged through the cavitation zone by the rotating shaft and (2) the mass transfer mechanism which dictates the rate of diffusion of dissolved gas out of and back into the lubricant. A comparison with available experimental results reveals that while the cavitation shape is fairly well predicted by the “shear” mechanism, this mechanism is incapable of generating the level of the experimentally measured pressures, particularly towards the end of the cavitation zone. The “mass transport” mechanism is found inadequate to explain the experimental observations. The effect of this mechanism on the pressure build up in the cavitation zone can be completely ignored.

Author(s):  
Lalit M. Pant ◽  
Marc Secanell ◽  
Sushanta K. Mitra

Study of gas diffusion is critical in understanding the process of mass transfer in porous media, which is an integral part of polymer electrolyte membrane fuel cells (PEMFCs). An experimental method is presented to study the mass transfer processes in micro-nano capillaries, which is further extended to study the transport in the porous media of fuel cells. A diffusion bridge setup, similar to the one presented by Remick and Geankoplis [1] has been used. The experimental setup facilitates the study of binary and multicomponent mixture transport through micro-nano capillaries and porous media. The setup can perform studies for two cases viz., pure diffusion and convection-diffusion. Using pressure controls in both channels, the pressure gradient across the capillaries is varied to study the convection diffusion process in detail. The results obtained from the study will be used to review various models of mass transport available in literature.


Membranes ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 560
Author(s):  
Adnan Alhathal Alanezi ◽  
Mohamed Bassyouni ◽  
Shereen M. S. Abdel-Hamid ◽  
Hassn Safi Ahmed ◽  
Mohamed Helmy Abdel-Aziz ◽  
...  

This paper’s primary objective is to examine the vapor delivery mechanism through a tubular membrane distillation (MD) module. Experiments were conducted utilizing a hydrophobic tubular membrane module with a pore size of 0.2 µm. To establish the mass transport mechanism of water vapor, tests were carried out first with pure water as a feed. The permeate flow was then determined using NaCl aqueous feed solutions. Distilled water flux at diverse feed temperatures, feed flow rates, and feed salt concentrations was investigated. The permeate flux improved linearly with rising temperature and flow rate of the feed, however, it declined with feed concentration. Increasing temperature from 40 to 70 °C increased the permeate flux by a factor of 2.2, while increasing the feed flow rate from 60 to 120 L/h increased the permeate flux by a factor ranging from 0.7 to 1.1 depending on feed temperature. Using the Dusty gas model (DGM) the mass transport of water vapor is estimated in the membrane pores. The results showed that the water vapor delivery is controlled by way of the Knudsen molecular diffusion transition mechanism and its version changed into one capable of predicting the permeate fluxes. The mass transfer coefficient calculated and located using the Knudsen molecular transition version agreed properly with the corresponding experimental value. The delivery resistances were affected by working parameters, along with feed temperature, flow rate, and concentration. The mass transfer resistance of the membrane became the predominant controlling step to the MD process.


2003 ◽  
Vol 3 (1-2) ◽  
pp. 201-207
Author(s):  
H. Nagaoka ◽  
T. Nakano ◽  
D. Akimoto

The objective of this research is to investigate mass transfer mechanism in biofilms under oscillatory flow conditions. Numerical simulation of turbulence near a biofilm was conducted using the low Reynold’s number k-ɛ turbulence model. Substrate transfer in biofilms under oscillatory flow conditions was assumed to be carried out by turbulent diffusion caused by fluid movement and substrate concentration profile in biofilm was calculated. An experiment was carried out to measure velocity profile near a biofilm under oscillatory flow conditions and the influence of the turbulence on substrate uptake rate by the biofilm was also measured. Measured turbulence was in good agreement with the calculated one and the influence of the turbulence on the substrate uptake rate was well explained by the simulation.


2020 ◽  
Vol 65 (7) ◽  
pp. 242-245
Author(s):  
A. I. Ageev ◽  
A. N. Osiptsov
Keyword(s):  

2020 ◽  
Vol 77 (3) ◽  
pp. 556-563 ◽  
Author(s):  
Naomi K. Pleizier ◽  
Charlotte Nelson ◽  
Steven J. Cooke ◽  
Colin J. Brauner

Hydrostatic pressure is known to protect fish from damage by total dissolved gas (TDG) supersaturation, but empirical relationships are lacking. In this study we demonstrate the relationship between depth, TDG, and gas bubble trauma (GBT). Hydroelectric dams generate TDG supersaturation that causes bubble growth in the tissues of aquatic animals, resulting in sublethal and lethal effects. We exposed fish to 100%, 115%, 120%, and 130% TDG at 16 and 63 cm of depth and recorded time to 50% loss of equilibrium and sublethal symptoms. Our linear model of the log-transformed time to 50% LOE (R2 = 0.94) was improved by including depth. Based on our model, a depth of 47 cm compensated for the effects of 4.1% (±1.3% SE) TDG supersaturation. Our experiment reveals that once the surface threshold for GBT from TDG supersaturation is known, depth protects rainbow trout (Oncorhynchus mykiss) from GBT by 9.7% TDG supersaturation per metre depth. Our results can be used to estimate the impacts of TDG on fish downstream of dams and to develop improved guidelines for TDG.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jing Li ◽  
Xiaoxia Chang ◽  
Haochen Zhang ◽  
Arnav S. Malkani ◽  
Mu-jeng Cheng ◽  
...  

AbstractRigorous electrokinetic results are key to understanding the reaction mechanisms in the electrochemical CO reduction reaction (CORR), however, most reported results are compromised by the CO mass transport limitation. In this work, we determined mass transport-free CORR kinetics by employing a gas-diffusion type electrode and identified dependence of catalyst surface speciation on the electrolyte pH using in-situ surface enhanced vibrational spectroscopies. Based on the measured Tafel slopes and reaction orders, we demonstrate that the formation rates of C2+ products are most likely limited by the dimerization of CO adsorbate. CH4 production is limited by the CO hydrogenation step via a proton coupled electron transfer and a chemical hydrogenation step of CO by adsorbed hydrogen atom in weakly (7 < pH < 11) and strongly (pH > 11) alkaline electrolytes, respectively. Further, CH4 and C2+ products are likely formed on distinct types of active sites.


1993 ◽  
Vol 253 (-1) ◽  
pp. 341 ◽  
Author(s):  
G. I. Barenblatt ◽  
M. Bertsch ◽  
R. Dal Passo ◽  
V. M. Prostokishin ◽  
M. Ughi

2015 ◽  
Vol 782 ◽  
pp. 260-299 ◽  
Author(s):  
Preyas N. Shah ◽  
Eric S. G. Shaqfeh

Surfaces that include heterogeneous mass transfer at the microscale are ubiquitous in nature and engineering. Many such media are modelled via an effective surface reaction rate or mass transfer coefficient employing the conventional ansatz of kinetically limited transport at the microscale. However, this assumption is not always valid, particularly when there is strong flow. We are interested in modelling reactive and/or porous surfaces that occur in systems where the effective Damköhler number at the microscale can be $O(1)$ and the local Péclet number may be large. In order to expand the range of the effective mass transfer surface coefficient, we study transport from a uniform bath of species in an unbounded shear flow over a flat surface. This surface has a heterogeneous distribution of first-order surface-reactive circular patches (or pores). To understand the physics at the length scale of the patch size, we first analyse the flux to a single reactive patch. We use both analytic and boundary element simulations for this purpose. The shear flow induces a 3-D concentration wake structure downstream of the patch. When two patches are aligned in the shear direction, the wakes interact to reduce the per patch flux compared with the single-patch case. Having determined the length scale of the interaction between two patches, we study the transport to a periodic and disordered distribution of patches again using analytic and boundary integral techniques. We obtain, up to non-dilute patch area fraction, an effective boundary condition for the transport to the patches that depends on the local mass transfer coefficient (or reaction rate) and shear rate. We demonstrate that this boundary condition replaces the details of the heterogeneous surfaces at a wall-normal effective slip distance also determined for non-dilute patch area fractions. The slip distance again depends on the shear rate, and weakly on the reaction rate, and scales with the patch size. These effective boundary conditions can be used directly in large-scale physics simulations as long as the local shear rate, reaction rate and patch area fraction are known.


2012 ◽  
Vol 86 (6) ◽  
Author(s):  
Roberto Camassa ◽  
M. Gregory Forest ◽  
Long Lee ◽  
H. Reed Ogrosky ◽  
Jeffrey Olander

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