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dc.contributor.author
Medina, Sabrina  
dc.contributor.author
Padilla, María Florencia  
dc.contributor.author
Avila, Adolfo María  
dc.contributor.author
Madrid, Rossana Elena  
dc.date.available
2024-02-08T14:03:20Z  
dc.date.issued
2022  
dc.identifier.citation
The effect of increasing ion capacity in the porous phase of a shock electrodialysis cell; III Brazil-Argentine Microfluidics Congress; VI Congreso de Microfluídica Argentina; Buenos Aires; Argentina; 2022; 64-65  
dc.identifier.uri
http://hdl.handle.net/11336/226431  
dc.description.abstract
Shock electrodialysis (SED) is an emerging electrokinetic purification method which is able to deionize solutions. This process only requires power for moving fluids through porous media, which avoid the need for high temperature (distillation) or high pressure (reverse osmosis, RO) systems. SED is essentially based on ion concentration polarization phenomenon. Concentration polarization is an interphase phenomenon which typically occurs when there is a mass transport limitation for the faster diffusing species in the fluid phase compared to the transport in the selective layer. Consequently, there is a reduction of the faster diffusing component in the boundary layer next to the selective layer and thus creating a depleted zone near the interphase. If a porous material is next to the interphase, now concentration polarization becomes higher due to the added diffusion limitation provided by the porous material and thus reducing even more the concentration of the faster diffusing species in the interphase. In our previous work, it was shown it is possible to extract a less concentrated electrolyte solution by continuous flow experiments in a miniaturized cell [1]. For this purpose, a biocarbon obtained through the pyrolysis of compressed residues from the sugarcane harvest was used as a porous phase to improve the polarization of the ion concentration. Through this system, the conductivity of a 0.1 mM KCl feed solution can be lowered by 25 percent over a period of 4 h working at a flow rate of 0.7 ccm and 5.0 V of applied voltage. This process was reversible by coming back to normal soon after the voltage was shut off. Different concentration ratios between the feed and the dilute phases can be obtained by changing the flow rate. This is an important advantage in terms of microfluidic device designs where operating flow rates are typically a few microliters. On the other hand, the separation performance between the feed and the more dilute outlet stream was improved by using a less permeable biochar material. In this work, the effect of increasing the ion capacity of the porous phase was studied by performing experiments through pulses of low concentration solutions (Fig. 1A). For this purpose, a zeolite material layer was included between two biochar disks. Fig. 1B shows the conductivity response when a pulse (1 cc) of low concentration solution (2 pS/cm) was injected into the feed. In the first injection, voltage was not applied. Voltage was switched on during the second injection. In this latter case, a significant depleted concentration stream at the cell outlet was observed. This is associated with the improved ion capacity of the porous phase due the presence of the zeolitic material.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Shock electrodialysis  
dc.subject
Ion polarization  
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Electrolyte separation  
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Zeolite  
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Otras Ingenierías y Tecnologías  
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Otras Ingenierías y Tecnologías  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
The effect of increasing ion capacity in the porous phase of a shock electrodialysis cell  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.type
info:eu-repo/semantics/conferenceObject  
dc.type
info:ar-repo/semantics/documento de conferencia  
dc.date.updated
2024-02-02T15:12:17Z  
dc.journal.pagination
64-65  
dc.journal.pais
Argentina  
dc.journal.ciudad
Buenos Aires  
dc.description.fil
Fil: Medina, Sabrina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina  
dc.description.fil
Fil: Padilla, María Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina  
dc.description.fil
Fil: Avila, Adolfo María. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina  
dc.description.fil
Fil: Madrid, Rossana Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto Superior de Investigaciones Biológicas. Universidad Nacional de Tucumán. Instituto Superior de Investigaciones Biológicas; Argentina  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://sites.google.com/view/microfluidics2022/book-of-abstracts  
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Autor  
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Autor  
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Autor  
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Autor  
dc.coverage
Internacional  
dc.type.subtype
Congreso  
dc.description.nombreEvento
III Brazil-Argentine Microfluidics Congress; VI Congreso de Microfluídica Argentina  
dc.date.evento
2022-11-05  
dc.description.ciudadEvento
Buenos Aires  
dc.description.paisEvento
Argentina  
dc.type.publicacion
Book  
dc.description.institucionOrganizadora
Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes  
dc.source.libro
Book of Abstracts: III Brazil-Argentine Microfluidics Congress and VI Congreso de Microfluídica Argentina  
dc.date.eventoHasta
2022-11-09  
dc.type
Congreso