Modeling of Divalent/Monovalent Ion Selectivity of Ion-Exchanger-Based Solvent Polymeric Membranes Doped with Coexchanger

2000 ◽  
Vol 72 (20) ◽  
pp. 4965-4972 ◽  
Author(s):  
Konstantin N. Mikhelson ◽  
Andrzej Lewenstam
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.


2011 ◽  
Vol 100 (3) ◽  
pp. 578a
Author(s):  
Michael Thomas ◽  
Dylan Jayatilaka ◽  
Ben Corry

2020 ◽  
Author(s):  
Arundhati Roy ◽  
Jie Shen ◽  
Himanshu Joshi ◽  
Woochul Song ◽  
Yu-Ming Tu ◽  
...  

The outstanding capacity of aquaporins (AQPs) for mediating highly selective superfast water transport1-7 has inspired recent development of supramolecular monovalent ion-excluding artificial water channels (AWCs). AWC-based bioinspired membranes are proposed for desalination, water purification, and other separations applications8-18. While some recent progress has been made in synthesizing AWCs that approach the water permeability and ion selectivity of AQPs, a hallmark feature of AQPs – high water transport while excluding protons has not been reproduced. We report on a class of biomimetic, helically folded pore-forming polymeric foldamers, that can serve as long sought-after highly selective ultrafast water-conducting channels exceeding those of AQPs (1.1 × 1010 H2O molecules/s for AQP17), with high water over monovalent ion transport selectivity (~108 water molecules over Cl- ion) conferred by the modularly tunable hydrophobicity of the interior pore surface. The best-performing AWC reported here delivers water transport at an exceptionally high rate, 2.5 times that of AQP1, while concurrently rejecting salts (NaCl and KCl) and even protons.


2020 ◽  
Author(s):  
Arundhati Roy ◽  
Jie Shen ◽  
Himanshu Joshi ◽  
Woochul Song ◽  
Yu-Ming Tu ◽  
...  

The outstanding capacity of aquaporins (AQPs) for mediating highly selective superfast water transport1-7 has inspired recent development of supramolecular monovalent ion-excluding artificial water channels (AWCs). AWC-based bioinspired membranes are proposed for desalination, water purification, and other separations applications8-18. While some recent progress has been made in synthesizing AWCs that approach the water permeability and ion selectivity of AQPs, a hallmark feature of AQPs – high water transport while excluding protons has not been reproduced. We report on a class of biomimetic, helically folded pore-forming polymeric foldamers, that can serve as long sought-after highly selective ultrafast water-conducting channels exceeding those of AQPs (1.1 × 1010 H2O molecules/s for AQP17), with high water over monovalent ion transport selectivity (~108 water molecules over Cl- ion) conferred by the modularly tunable hydrophobicity of the interior pore surface. The best-performing AWC reported here delivers water transport at an exceptionally high rate, 2.5 times that of AQP1, while concurrently rejecting salts (NaCl and KCl) and even protons.


1987 ◽  
Vol 65 (5) ◽  
pp. 889-893 ◽  
Author(s):  
Walter G. Carlini ◽  
Bruce R. Ransom

Double-barreled ion-exchanger based K+ -selective microelectrodes (K+ ISMs) of a variety of tip diameters were used to study the dependency of ion selectivity upon tip size. The selectivity of K+ ISMs depended on tip size and barrel configuration. Within the range of tip diameters tested (~ 0.5–6 μm) all K+ ISMs constructed of two barrels glued side by side ("figure-eight glass") exhibited sensitivity to K+ and NH4+. Figure-eight K+ ISMs with tip diameters < 1.5 μm were not sensitive to tetramethylammonium, tetraethylammonium, or choline, whereas K+ ISMs with tip diameters ≥ 1.5 μm sensed all of the quaternary amines. Tip size dependent selectivity was not present in K+ ISMs made from thick septum theta glass. The explanation for tip size dependent changes in ion selectivity is unknown but a discussion of theoretical possibilities is given.


2012 ◽  
Vol 102 (3) ◽  
pp. 603a-604a
Author(s):  
Rocio K. Finol-Urdaneta ◽  
Ahmed Al-Sabi ◽  
Sergei Noskov ◽  
Robert J. French

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