Název: | Electric Potential Profiles in a Model Single-Path Electrodialysis Unit |
Autoři: | Pagáč, Jan Kovář, Petr Slouka, Zdeněk |
Citace zdrojového dokumentu: | PAGÁČ, J. KOVÁŘ, P. SLOUKA, Z. Electric Potential Profiles in a Model Single-Path Electrodialysis Unit. Membranes, 2022, roč. 12, č. 11, s. nestránkováno. ISSN: 2077-0375 |
Datum vydání: | 2022 |
Nakladatel: | MDPI |
Typ dokumentu: | článek article |
URI: | http://hdl.handle.net/11025/51350 |
ISSN: | 2077-0375 |
Klíčová slova v dalším jazyce: | electrodialysis;electric potential;diluate;overlimiting current;desalination |
Abstrakt: | Electrodialysis is an important electromembrane separation process anticipated to play a significant role in developing future technologies. It produces ion-depleted and ion-concentrated product streams, intrinsically suggesting the formation of spatial gradients of relevant quantities. These quantities affect local conditions in an electrodialysis unit. To investigate the spatial distribution of electric potentials, we constructed a model electrodialysis system with a single diluate channel that included ports for inserting reference electrodes measuring potential profiles. We validated our system and measurement methods in a series of control experiments under a solution flow rate of 250 μL/min and current densities between 10 and 52 A/m2. The collected data showed that the electric potential in the diluate channel did not change in the vertical direction (direction of gravity force), and only minimally varied in the diluate channel center in the flow direction. Although we could not reconstruct the potential profile within ion-depleted layers due to the resolution of the method, we found appreciable potential variation across the diluate channel. The most significant potential drops were localized on the membranes with the developed ion-depleted zones. Interestingly, these potential drops abruptly increased when we applied current loads, yielding almost complete desalination. The increase in the resistance accompanied by relatively large fluctuations in the measured potential indicated the system transition into limiting and overlimiting regions, and the onset of overlimiting convection. |
Abstrakt v dalším jazyce: | Electrodialysis is an important electromembrane separation process anticipated to play a significant role in developing future technologies. It produces ion-depleted and ion-concentrated product streams, intrinsically suggesting the formation of spatial gradients of relevant quantities. These quantities affect local conditions in an electrodialysis unit. To investigate the spatial distribution of electric potentials, we constructed a model electrodialysis system with a single diluate channel that included ports for inserting reference electrodes measuring potential profiles. We validated our system and measurement methods in a series of control experiments under a solution flow rate of 250 μL/min and current densities between 10 and 52 A/m2. The collected data showed that the electric potential in the diluate channel did not change in the vertical direction (direction of gravity force), and only minimally varied in the diluate channel center in the flow direction. Although we could not reconstruct the potential profile within ion-depleted layers due to the resolution of the method, we found appreciable potential variation across the diluate channel. The most significant potential drops were localized on the membranes with the developed ion-depleted zones. Interestingly, these potential drops abruptly increased when we applied current loads, yielding almost complete desalination. The increase in the resistance accompanied by relatively large fluctuations in the measured potential indicated the system transition into limiting and overlimiting regions, and the onset of overlimiting convection. |
Práva: | © authors |
Vyskytuje se v kolekcích: | Články / Articles OBD |
Soubory připojené k záznamu:
Soubor | Velikost | Formát | |
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SLOUKA_membranes-12-01136.pdf | 1,45 MB | Adobe PDF | Zobrazit/otevřít |
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http://hdl.handle.net/11025/51350
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