Effect of Pore‐Size Distribution on Metal Ion Removal in Flow‐Through Porous Electrodes

1986 ◽  
Vol 133 (8) ◽  
pp. 1649-1653 ◽  
Author(s):  
Jacob Jorne ◽  
Emad Roayaie
2021 ◽  
Author(s):  
Martin Lanzendörfer

<p>Following the capillary bundle concept, i.e. idealizing the flow in a saturated porous media in a given direction as the Hagen-Poiseuille flow through a number of tubular capillaries, one can very easily solve what we would call the <em>forward problem</em>: Given the number and geometry of the capillaries (in particular, given the pore size distribution), the rheology of the fluid and the hydraulic gradient, to determine the resulting flux. With a Newtonian fluid, the flux would follow the linear Darcy law and the porous media would then be represented by one constant only (the permeability), while materials with very different pore size distributions can have identical permeability. With a non-Newtonian fluid, however, the flux resulting from the forward problem (while still easy to solve) depends in a more complicated nonlinear way upon the pore sizes. This has allowed researchers to try to solve the much more complicated <em>inverse problem</em>: Given the fluxes corresponding to a set of non-Newtonian rheologies and/or hydraulic gradients, to identify the geometry of the capillaries (say, the effective pore size distribution).</p><p>The potential applications are many. However, the inverse problem is, as they usually are, much more complicated. We will try to comment on some of the challenges that hinder our way forward. Some sets of experimental data may not reveal any information about the pore sizes. Some data may lead to numerically ill-posed problems. Different effective pore size distributions correspond to the same data set. Some resulting pore sizes may be misleading. We do not know how the measurement error affects the inverse problem results. How to plan an optimal set of experiments? Not speaking about the important question, how are the observed effective pore sizes related to other notions of pore size distribution.</p><p>All of the above issues can be addressed (at least initially) with artificial data, obtained e.g. by solving the forward problem numerically or by computing the flow through other idealized pore geometries. Apart from illustrating the above issues, we focus on <em>two distinct aspects of the inverse problem</em>, that should be regarded separately. First: given the forward problem with <em>N</em> distinct pore sizes, how do different algorithms and/or different sets of experiments perform in identifying them? Second: given the forward problem with a smooth continuous pore size distribution (or, with the number of pore sizes greater than <em>N</em>), how should an optimal representation by <em>N</em> effective pore sizes be defined, regardless of the method necessary to find them?</p>


2007 ◽  
Vol 44 (12) ◽  
pp. 1446-1461 ◽  
Author(s):  
Greg Siemens ◽  
James A. Blatz ◽  
Douglas Ruth

Swelling mechanisms occurring on the pore scale or at the molecular level of high plasticity, unsaturated soils often control macroscopic behaviour. In this paper, a new capillary tube model is proposed. The model is used to represent laboratory-scale infiltration tests on a bentonite-rich soil. The goal is to develop a greater understanding of bulk behaviour by closely examining microscopic behaviour. A decrease in hydraulic conductivity with increasing water content has been observed in laboratory studies on flow through shrink–swell materials. The proposed mechanism causing a decrease in conductivity is a change in pore-size distribution. The unique feature of the new capillary-tube model is that, as water flows down the tube, the tube’s cross-sectional area contracts to restrict flow, thus representing the change in pore-size distribution observed in the physical tests. Flow data from the capillary tube are used to model the laboratory results, and new insight is gained into bulk flow behaviour. Finally, a comparison with a three-dimensional network model for bentonite-coated sand mixtures is presented.


2000 ◽  
Vol 45 (14) ◽  
pp. 2241-2257 ◽  
Author(s):  
Hyun-Kon Song ◽  
Hee-Young Hwang ◽  
Kun-Hong Lee ◽  
Le H. Dao

2001 ◽  
Vol 699 ◽  
Author(s):  
Hyun-Kon Song ◽  
Kun-Hong Lee

AbstractWe have developed the electrochemical porosimetry analyzing microstructures of porous electrodes, which can give geometric information most meaningful in electrochemical systems. The methodology is based on the transmission line model with pore size distribution (TLM-PSD) that relates electrochemical impedance data with microstructural information. Pore length (lp), as well as pore size distribution, can be obtained by fitting the TLM-PSD to the experimental impedance data of a porous electrode. This geometric information was validated for the microporous, mesoporous and macroporous samples by comparing with the data obtained from conventional porosimetry. It was also shown that the electrochemical porosimetry could be used as a nondestructive probe to investigate the construction of electrochemical devices.


2021 ◽  
Vol 7 (1) ◽  
pp. 15
Author(s):  
Joshua Bates ◽  
Foivos Markoulidis ◽  
Constantina Lekakou ◽  
Giuliano M. Laudone

The challenge of optimizing the pore size distribution of porous electrodes for different electrolytes is encountered in supercapacitors, lithium-ion capacitors and hybridized battery-supercapacitor devices. A volume-averaged continuum model of ion transport, taking into account the pore size distribution, is employed for the design of porous electrodes for electrochemical double-layer capacitors (EDLCs) in this study. After validation against experimental data, computer simulations investigate two types of porous electrodes, an activated carbon coating and an activated carbon fabric, and three electrolytes: 1.5 M TEABF4 in acetonitrile (AN), 1.5 M TEABF4 in propylene carbonate (PC), and 1 M LiPF6 in ethylene carbonate:ethyl methyl carbonate (EC:EMC) 1:1 v/v. The design exercise concluded that it is important that the porous electrode has a large specific area in terms of micropores larger than the largest desolvated ion, to achieve high specific capacity, and a good proportion of mesopores larger than the largest solvated ion to ensure fast ion transport and accessibility of the micropores.


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