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Dielectric polarization-based separations in an ionic solution

A novel non-electrophoretic, electric field-based separation mechanism capable of transporting ions based on their dielectric properties is presented here for the first time. Though this polarization-based mechanism behaves similarly to dielectrophoresis, the separation mechanism is remarkably very...

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Detalles Bibliográficos
Autores principales: Anand, Gaurav, Safaripour, Samira, Snoeyink, Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363714/
https://www.ncbi.nlm.nih.gov/pubmed/37492504
http://dx.doi.org/10.1039/d3ra03169a
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author Anand, Gaurav
Safaripour, Samira
Snoeyink, Craig
author_facet Anand, Gaurav
Safaripour, Samira
Snoeyink, Craig
author_sort Anand, Gaurav
collection PubMed
description A novel non-electrophoretic, electric field-based separation mechanism capable of transporting ions based on their dielectric properties is presented here for the first time. Though this polarization-based mechanism behaves similarly to dielectrophoresis, the separation mechanism is remarkably very efficient at small length scales compared to any dielectrophoretic separation mechanism for particles. For an applied electric field of strength as low as ∼0.75 MV m(−1) across a 100 μm channel, the working solute – sodium fluorescein – is shown to decrease in its concentration by ≈20% in electric field region relative to the non electric field region. The existing macroscopic theoretical models like electrohydrodynamics and equilibrium thermodynamics are shown to underestimate the concentration change by two orders of magnitude for the same electric field strength. This surprisingly large difference between theory and experimental results suggests that the electric field-based equilibrium thermodynamic model lacks a key physics.
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spelling pubmed-103637142023-07-25 Dielectric polarization-based separations in an ionic solution Anand, Gaurav Safaripour, Samira Snoeyink, Craig RSC Adv Chemistry A novel non-electrophoretic, electric field-based separation mechanism capable of transporting ions based on their dielectric properties is presented here for the first time. Though this polarization-based mechanism behaves similarly to dielectrophoresis, the separation mechanism is remarkably very efficient at small length scales compared to any dielectrophoretic separation mechanism for particles. For an applied electric field of strength as low as ∼0.75 MV m(−1) across a 100 μm channel, the working solute – sodium fluorescein – is shown to decrease in its concentration by ≈20% in electric field region relative to the non electric field region. The existing macroscopic theoretical models like electrohydrodynamics and equilibrium thermodynamics are shown to underestimate the concentration change by two orders of magnitude for the same electric field strength. This surprisingly large difference between theory and experimental results suggests that the electric field-based equilibrium thermodynamic model lacks a key physics. The Royal Society of Chemistry 2023-07-24 /pmc/articles/PMC10363714/ /pubmed/37492504 http://dx.doi.org/10.1039/d3ra03169a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Anand, Gaurav
Safaripour, Samira
Snoeyink, Craig
Dielectric polarization-based separations in an ionic solution
title Dielectric polarization-based separations in an ionic solution
title_full Dielectric polarization-based separations in an ionic solution
title_fullStr Dielectric polarization-based separations in an ionic solution
title_full_unstemmed Dielectric polarization-based separations in an ionic solution
title_short Dielectric polarization-based separations in an ionic solution
title_sort dielectric polarization-based separations in an ionic solution
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363714/
https://www.ncbi.nlm.nih.gov/pubmed/37492504
http://dx.doi.org/10.1039/d3ra03169a
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