Periodical Pressure-Driven Flows in Microchannel with Wall Slip Velocity and Electro-Viscous Effects

2010 ◽  
Vol 22 (6) ◽  
pp. 829-837 ◽  
Author(s):  
Lei Wang ◽  
Jian-kang Wu
Keyword(s):  
Slip Velocity ◽  
Wall Slip ◽  
Viscous Effects ◽  
Pressure Driven

scholarly journals Quantification of shear viscosity and wall slip velocity of highly concentrated suspensions with non-Newtonian matrices in pressure driven flows

2021 ◽  
Author(s):  
Patrick Wilms ◽  
Jan Wieringa ◽  
Theo Blijdenstein ◽  
Kees van Malssen ◽  
Reinhard Kohlus
Keyword(s):  
Shear Stress ◽  
Liquid Phase ◽  
Shear Rate ◽  
Shear Viscosity ◽  
Slip Velocity ◽  
Volume Fraction ◽  
Solid Volume Fraction ◽  
Wall Slip ◽  
Flow Index ◽  
Concentrated Suspensions

AbstractThe rheological characterization of concentrated suspensions is complicated by the heterogeneous nature of their flow. In this contribution, the shear viscosity and wall slip velocity are quantified for highly concentrated suspensions (solid volume fractions of 0.55–0.60, D4,3 ~ 5 µm). The shear viscosity was determined using a high-pressure capillary rheometer equipped with a 3D-printed die that has a grooved surface of the internal flow channel. The wall slip velocity was then calculated from the difference between the apparent shear rates through a rough and smooth die, at identical wall shear stress. The influence of liquid phase rheology on the wall slip velocity was investigated by using different thickeners, resulting in different degrees of shear rate dependency, i.e. the flow indices varied between 0.20 and 1.00. The wall slip velocity scaled with the flow index of the liquid phase at a solid volume fraction of 0.60 and showed increasingly large deviations with decreasing solid volume fraction. It is hypothesized that these deviations are related to shear-induced migration of solids and macromolecules due to the large shear stress and shear rate gradients.

Application of CFD-DSMC coupling method in micro-scale gas flow and combustion

2020 ◽  
Vol 34 (27) ◽  
pp. 2050301
Author(s):  
Shaoyi Suo ◽  
Linsong Jiang ◽  
Maozhao Xie
Keyword(s):  
Boundary Layer ◽  
Chemical Reaction ◽  
Wall Temperature ◽  
Slip Velocity ◽  
Gas Flow ◽  
Wall Slip ◽  
Reaction Products ◽  
Microscopic Method ◽  
Flow Heat ◽  
The Impact

The reversible elementary reaction mechanism of six components and seven steps of H2/O2 are applied by using a CFD-DSMC coupling iteration method to study the impact of boundary on flow, heat transfer and chemical reaction in a microtube. The microtube consists of a converging section and a straight section, which represents the gap on the contact surface of the pellets in porous media. It shows that after coupling, with the designed conditions in this paper, the influence of wall temperature is more obvious than that of wall slip velocity on the coupling results from the analysis of chemical reaction, yet the velocity field in the boundary layer is more affected by the wall slip velocity. In addition, the velocity in the central region of the flow decreases while the concentration of reaction products increases after coupling, due to the increasing of the velocity in the boundary layer and the influence of wall temperature, respectively. By the coupling of CFD-DSMC methods, more details and influence of the boundary can be considered, and the computational efficiency is higher than that of the single microscopic method.

Experimental study and molecular dynamics simulation of wall slip in a micro-extrusion flowing process

2011 ◽  
Vol 225 (5) ◽  
pp. 1175-1190 ◽  
Author(s):  
D Zhao ◽  
Y Jin ◽  
M Wang ◽  
M Song
Keyword(s):  
Molecular Dynamics ◽  
Shear Stress ◽  
Molecular Dynamics Simulation ◽  
Slip Velocity ◽  
Polymer Melts ◽  
Critical Shear Stress ◽  
Wall Slip ◽  
Dynamics Simulation ◽  
Desorption Mechanism ◽  
Adsorption Desorption

Wall slip is one of the most important characteristics of polymer melts’ elasticity behaviours as well as the most significant factor which affects the flow of polymer melts. Based on the traditional Mooney method, through a double-barrel capillary rheometer, the relationship between velocities of wall slip, shear stress, shear rate, diameters of dies, and temperature of polypropylene (PP), high-density polyethylene (HDPE), polystyrene (PS), and polymethylmethacrylate (PMMA) is explored. The results indicate that the velocities of the wall slip of PP and HDPE increase apparently with shear stress and slightly with temperature. Meanwhile, the rise of temperature results in the decrease of critical shear stress. The wall-slip velocities of PS and PMMA are negative which means that the Mooney method based on the adsorption–desorption mechanism has determinate limitation to calculate the wall-slip velocity. Based on the entanglement–disentanglement mechanism, a new wall-slip model is built. With the new model, the calculation values of velocity of PP and HDPE correspond to the experimental values very well and the velocities of PS and PMMA are positive. The velocities of PS and PMMA increase obviously with the rise of shear stress. The rise of temperature results in the increase of velocity and decrease of critical shear stress. Then, the molecular dynamics simulation is used to investigate the combining energy between four polymer melts and the inside wall. The results show that at the given temperature and pressure, the molecules of PS and PMMA combine with atoms of the wall more tightly than those of PP and HDPE which means when wall slip occurs, the molecules of PS and PMMA near the wall will adsorb to the surface of the wall. However, those of PP and HDPE will be easy to slip. Therefore, the wall-slip mechanism of PP and HDPE is the adsorption–desorption mechanism, and that of PS and PMMA is the entanglement–disentanglement mechanism. According to the different wall-slip mechanisms of four polymers, an all-sided calculation method of wall-slip velocity is raised which consummates the theory of wall slip of polymer melts.

Development Length in Planar Channel Flows of Newtonian Fluids Under the Influence of Wall Slip

2012 ◽  
Vol 134 (10) ◽  
Author(s):  
L. L. Ferrás ◽  
A. M. Afonso ◽  
M. A. Alves ◽  
J. M. Nóbrega ◽  
F. T. Pinho
Keyword(s):  
Slip Velocity ◽  
Numerical Study ◽  
Fluid Flows ◽  
Wall Slip ◽  
Newtonian Fluids ◽  
Planar Channel ◽  
Development Length ◽  
Navier Slip ◽  
Slip Boundary ◽  
Low Reynolds Number Flows

This technical brief presents a numerical study regarding the required development length (L=Lfd/H) to reach fully developed flow conditions at the entrance of a planar channel for Newtonian fluids under the influence of slip boundary conditions. The linear Navier slip law is used with the dimensionless slip coefficient k¯l=kl(μ/H), varying in the range 0<k¯l≤1. The simulations were carried out for low Reynolds number flows in the range 0<Re≤100, making use of a rigorous mesh refinement with an accuracy error below 1%. The development length is found to be a nonmonotonic function of the slip velocity coefficient, increasing up to k¯l≈0.1-0.4 (depending on Re) and decreasing for higher k¯l. We present a new nonlinear relationship between L, Re, and k¯l that can accurately predict the development length for Newtonian fluid flows with slip velocity at the wall for Re of up to 100 and k¯l up to 1.

Molecular Dynamics Simulation of Rarefied Gaseous Flows in Nano-Channels

2013 ◽  
Vol 446-447 ◽  
pp. 12-17
Author(s):  
Zhi Hong Mao ◽  
Fu Bing Bao ◽  
Yuan Lin Huang
Keyword(s):  
Molecular Dynamics ◽  
Molecular Dynamics Simulation ◽  
Slip Velocity ◽  
Average Velocity ◽  
Single Layer ◽  
Simulation Method ◽  
Dynamics Simulation ◽  
Channel Height ◽  
Gaseous Flows ◽  
Pressure Driven

Molecular dynamics simulation method was used to study the rarefied gaseous flows in nanochannels. A pressure-driven force was introduced to drive the gas to flow between two parallel walls. The effects of driven force magnitude and channel height were investigated. The results show that a single layer of gaseous molecules is adsorbed on the wall surface. The density of adsorption layer decreases with the increase of channel height, but doesnt vary with driven force. The velocity profile across the channel has the traditional parabolic shape. The average velocity and gas slip velocity on the wall increase linearly with the increase of pressure-driven force. The gas slip velocity decreases linearly with the increase of channel height. The ratio of slip to average velocity decreases linearly with the increase of channel height.

Rheology of Commercial and Model Ice Creams

2008 ◽  
Vol 18 (1) ◽  
pp. 12913-1-12913-11 ◽  
Author(s):  
P.J. Martin ◽  
K.N. Odic ◽  
A.B. Russell ◽  
I.W. Burns ◽  
D.I. Wilson
Keyword(s):  
Milk Fat ◽  
Sucrose Solution ◽  
Shear Thickening ◽  
Wall Slip ◽  
Ice Cream ◽  
Viscous Effects ◽  
Capillary Rheometry ◽  
Shear Rates ◽  
High Shear Rates ◽  
Slip Effects

Abstract The rheologies of a shear-frozen commercial ice cream and of a model ice cream foam have been studied at − 5ºC and other temperatures by capillary rheometry on a commercial manufacturing line and in a Multi-Pass Rheometer, respectively. Both were 50 vol% aerated emulsions of milk fat in an aqueous sucrose solution, but the model ice cream foam was without ice crystals. The data indicate significant wall slip effects which have been analysed using the classical Mooney method, the Jastrzebski variant and one based on Tikhonov regularization. The latter approach yields ‘most convincing results’, including a previously unreported region of shear thickening at very high shear rates of ~ 3000 s-1 for the model ice cream foam, when the capillary number indicates a possible transition in the flow around bubbles from domination by interfacial effects to viscous effects. Viscous heating effects were observed at relatively low shear rates for the commercial ice cream, but not the model ice cream foam. This was attributed to the melting of the ice crystal phase in the commercial ice cream, and, hence, absent from the model ice cream foam.

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