Apparent wall slip velocity coefficients in concentrated suspensions of noncolloidal particles

1995 ◽  
Vol 39 (6) ◽  
pp. 1123-1132 ◽  
Author(s):  
S. C. Jana ◽  
B. Kapoor ◽  
A. Acrivos
2021 ◽  
Author(s):  
Patrick Wilms ◽  
Jan Wieringa ◽  
Theo Blijdenstein ◽  
Kees van Malssen ◽  
Reinhard Kohlus

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.


2020 ◽  
Vol 34 (27) ◽  
pp. 2050301
Author(s):  
Shaoyi Suo ◽  
Linsong Jiang ◽  
Maozhao Xie

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.


Author(s):  
D Zhao ◽  
Y Jin ◽  
M Wang ◽  
M Song

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.


2012 ◽  
Vol 134 (10) ◽  
Author(s):  
L. L. Ferrás ◽  
A. M. Afonso ◽  
M. A. Alves ◽  
J. M. Nóbrega ◽  
F. T. Pinho

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.


Author(s):  
Paulo R. Souza Mendes ◽  
Jose´ R. R. Siffert ◽  
Eduardo S. S. Dutra

We employ a recently proposed viscosity function (Souza Mendes and Dutra, 2004) to analyze the fully developed flow of yield-stress liquids through tubes. We first show that its dimensionless form gives rise to the so-called jump number, a novel material property that measures the shear rate jump that the material undergoes as the yield stress is reached. We integrate numerically the momentum conservation equation that governs this flow together with the generalized Newtonian Liquid model and the above mentioned viscosity function. We obtain velocity and viscosity profiles for the entire range of the jump number. We show that the friction factor f.Re curves display sharp peaks as the shear stress value at the tube wall approaches the yield stress. Finally, we demonstrate the existence of sharp flow rate increases (or apparent slip) as the wall shear stress is increased in the vicinity of the yield stress.


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