scholarly journals Size-Based Ion Selectivity of Micropore Electric Double Layers in Capacitive Deionization Electrodes

2017 ◽  
Vol 164 (9) ◽  
pp. E270-E275 ◽  
Author(s):  
Matthew E. Suss
2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Eric N. Guyes ◽  
Amit N. Shocron ◽  
Yinke Chen ◽  
Charles E. Diesendruck ◽  
Matthew E. Suss

AbstractEmerging water purification applications often require tunable and ion-selective technologies. For example, when treating water for direct use in irrigation, often monovalent Na+ must be removed preferentially over divalent minerals, such as Ca2+, to reduce both ionic conductivity and sodium adsorption ratio (SAR). Conventional membrane-based water treatment technologies are either largely non-selective or not dynamically tunable. Capacitive deionization (CDI) is an emerging membraneless technology that employs inexpensive and widely available activated carbon electrodes as the active element. We here show that a CDI cell leveraging sulfonated cathodes can deliver long-lasting, tunable monovalent ion selectivity. For feedwaters containing Na+ and Ca2+, our cell achieves a Na+/Ca2+ separation factor of up to 1.6. To demonstrate the cell longevity, we show that monovalent selectivity is retained over 1000 charge–discharge cycles, the highest cycle life achieved for a membraneless CDI cell with porous carbon electrodes to our knowledge, while requiring an energy consumption of ~0.38 kWh/m3 of treated water. Furthermore, we show substantial and simultaneous reductions of ionic conductivity and SAR, such as from 1.75 to 0.69 mS/cm and 19.8 to 13.3, respectively, demonstrating the potential of such a system towards single-step water treatment of brackish and wastewaters for direct use in irrigation.


1995 ◽  
Vol 335 ◽  
pp. 422-431 ◽  
Author(s):  
Michael R. Philpott ◽  
James N. Glosli ◽  
Sheng-Bai Zhu

A partition function for a system of rigid rod-like particles with partial orientation about an axis is derived through the use of a modified lattice model. In the limit of perfect orientation the partition function reduces to the ideal mixing law ; for complete disorientation it corresponds to the polymer mixing law for rigid chains. A general expression is given for the free energy of mixing as a function of the mole numbers, the axis ratio of the solute particles, and a disorientation parameter. This function passes through a minimum followed by a maximum with increase in the disorientation parameter, provided the latter exceeds a critical value which is 2e for the pure solute and which increases with dilution. Assigning this parameter the value which minimizes the free energy, the chemical potentials display discontinuities a t the concentration a t which the minimum first appears. Separation into an isotropic phase and a some what more concentrated anisotropic phase arises because of the discontinuity, in confirmation of the theories of Onsager and Isihara, which treat only the second virial coefficient. Phase separation thus arises as a consequence of particle asymmetry, unassisted by an energy term . Whereas for a large-particle asymmetry both phases in equilibrium are predicted to be fairly dilute when mixing is athermal, a comparatively small positive energy of interaction causes the concentration in the anisotropic phase to increase sharply, while the concentration in the isotropic phase becomes vanishingly small. The theory offers a statistical mechanical basis for interpreting precipitation of rod-like colloidal particles with the formation of fibrillar structures such as are prominent in the fibrous proteins. The asymmetry of tobacco mosaic virus particles (with or without inclusion of their electric double layers) is insufficient alone to explain the well-known phase separation which occurs from their dilute solutions at very low ionic strengths. Higher-order interaction between electric double layers appears to be a major factor in bringing about dilute phase separation for these and other asymmetric colloidal particles bearing large charges, as was pointed out previously by Oster.


Soil Science ◽  
2001 ◽  
Vol 166 (4) ◽  
pp. 249-254 ◽  
Author(s):  
Xin Jiang ◽  
Jianmin Zhou ◽  
Maoxu Zhu ◽  
Wenxiang He ◽  
Guifen Yu

Author(s):  
Punarvasu Joshi ◽  
Trupthi Mathew ◽  
Leo Petrossian ◽  
Shalini Prasad ◽  
Michael Goryll ◽  
...  

In this work we present preliminary results demonstrating the influence of electrical double layer overlap on the electromigration of polystyrene beads (PSB) through an array of 25 cylindrical nanopores. Each of the cylindrical nanopores of the array used in this study is 360nm long with a diameter of 90nm. We observe frequent Coulter events for solutions of higher ionic strength and absence of Coulter events at low ionic strength solution. At higher ionic strengths, the electric double layers in the nanopore are thin and ion transport through the nanopore follows the bulk behavior of the ionic solution. For solutions of lower ionic strength, the electric double layers are comparable to the nanopore dimensions and start to overlap, suggesting surface charge interaction with the polystyrene beads that pass through the nanopore. The work continues towards detailed statistical analysis of the characteristic events observed for different concentrations.


Author(s):  
A Mart√≠n-Molina ◽  
M Quesada-P√©rez ◽  
R Hidalgo-Álvarez

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