Effective dispersion and separation resolution in continuous particle fractionation

2015 ◽  
Vol 19 (5) ◽  
pp. 1035-1046 ◽  
Author(s):  
Stefano Cerbelli ◽  
Fabio Garofalo ◽  
Massimiliano Giona
2004 ◽  
Vol 76 (11) ◽  
pp. 3236-3243 ◽  
Author(s):  
Myeong Hee Moon ◽  
Hyun-Joo Kim ◽  
So-Yeon Kwon ◽  
Se-Jin Lee ◽  
Yoon-Seok Chang ◽  
...  

1987 ◽  
Vol 59 (2) ◽  
pp. 344-350 ◽  
Author(s):  
Stephen R. Springston ◽  
Marcus N. Myers ◽  
J. Calvin. Giddings

Carbon ◽  
2012 ◽  
Vol 50 (1) ◽  
pp. 3-33 ◽  
Author(s):  
Sang Won Kim ◽  
Taehoon Kim ◽  
Yern Seung Kim ◽  
Hong Soo Choi ◽  
Hyeong Jun Lim ◽  
...  

The dispersion of a pulse of ethylene injected into nitrogen, flowing in the laminar régime through straight and curved tubes, has been investigated at pressures of 1.0 and 4.4 atm. From the study of the concentration profiles with a thermal conductivity detector (katharometer) it is found that the experimental results for gas velocities between 1.00 and 16.00 cm/s agree well with the analytical solution to this problem for a straight tube given by Sir Geoffrey Taylor and extended by Aris. In particular, at low velocities, the effective dispersion coefficients tend to the molecular diffusivities. The presence of a bend slightly reduces the effective longitudinal dispersion coefficient and the introduction of constrictions enhances it. Data are also given on a number of other gas pairs. It is concluded that measurements of dispersion provide an accurate and simple way of studying diffusion in gas mixtures.


2021 ◽  
Author(s):  
Alexandre Puyguiraud ◽  
Lazaro Perez ◽  
Juan J. Hidalgo ◽  
Marco Dentz

<p>We utilize effective dispersion coefficients to capture the evolution of the mixing interface between two initially segregated species due to the coupled effect of pore-scale heterogeneity and molecular diffusion. These effective dispersion coefficients are defined as the average spatial variance of the solute plume that evolves from a pointlike injection (the transport Green function). We numerically investigate the effective longitudinal dispersion coefficients in two porous media of different structure heterogeneity  and through different Péclet number regimes for each medium. We find that, as distance traveled increases (or time spent), the solute experiences the pore-scale velocity field heterogeneity due to advection and transverse diffusion, resulting in an evolution of the dispersion coefficients. They evolve from the value of molecular diffusion at early time, then undergo an advection dominated regime, to finally reach the value of hydrodynamic dispersion at late times. This means that, at times smaller than the characteristic diffusion time, the effective dispersion coefficients can be notably smaller than the hydrodynamic dispersion coefficient. Therefore, mismatches between pore-scale reaction data from experiment or simulations and Darcy scale predictions based on temporally constant hydrodynamic dispersion can be explained through these differences. We use the effective dispersion coefficients to approximate the transport Green function and to quantify the incomplete mixing occurring at the pore-scale. We evaluate the evolution of two initially segregated species via this methodology. The approach correctly predicts the amount of chemical reaction occuring in reactive bimolecular particle tracking simulations. These results shed light on the upscaling of pore-scale incomplete mixing and demonstrates that the effective dispersion is an accurate measure for the width of the mixing interface between two reactants. </p>


2015 ◽  
Vol 72 ◽  
pp. 855-861 ◽  
Author(s):  
Yan Niu ◽  
Xiaofang Zhang ◽  
Xu He ◽  
Jiangqi Zhao ◽  
Wei Zhang ◽  
...  

Author(s):  
Chiu-On Ng

An asymptotic analysis is presented for the advection–diffusion transport of a chemical species in flow through a small-diameter tube, where the flow consists of steady and oscillatory components, and the species may undergo linear reversible (phase exchange or wall retention) and irreversible (decay or absorption) reactions at the tube wall. Both developed and transient concentrations are considered in the analysis; the former is governed by the Taylor dispersion model, while the latter is required in order to formulate proper initial data for the developed mean concentration. The various components of the effective dispersion coefficient, valid when the developed state is attained, are derived as functions of the Schmidt number, flow oscillation frequency, phase partitioning and kinetics of the two reactions. Being more general than those available in the literature, this effective dispersion coefficient incorporates the combined effects of wall retention and absorption on the otherwise classical Taylor dispersion mechanism. It is found that if the phase exchange reaction kinetics is strong enough, the dispersion coefficient is probably to be increased by orders of magnitude by changing the tube wall from being non-retentive to being just weakly retentive.


Sign in / Sign up

Export Citation Format

Share Document