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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Published inRSC advances Vol. 13; no. 32; pp. 22185 - 22192
Main Authors Anand, Gaurav, Safaripour, Samira, Snoeyink, Craig
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 19.07.2023
The Royal Society of Chemistry
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Abstract 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. 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.
AbstractList 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. 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.
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.
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. 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.
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 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.
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.
Author Snoeyink, Craig
Anand, Gaurav
Safaripour, Samira
AuthorAffiliation Department of Mechanical and Aerospace Engineering
University at Buffalo
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  contributor:
    fullname: Pethig
– volume: 77
  start-page: 616
  issue: 6
  year: 2023
  ident: D3RA03169A/cit39/1
  publication-title: Appl. Spectrosc.
  doi: 10.1177/00037028231175178
  contributor:
    fullname: Anand
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Snippet A novel non-electrophoretic, electric field-based separation mechanism capable of transporting ions based on their dielectric properties is presented here for...
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StartPage 22185
SubjectTerms Chemistry
Dielectric polarization
Dielectric properties
Dielectrophoresis
Electric field strength
Electrohydrodynamics
Separation
Thermodynamic equilibrium
Thermodynamic models
Thermodynamics
Title Dielectric polarization-based separations in an ionic solution
URI https://www.ncbi.nlm.nih.gov/pubmed/37492504
https://www.proquest.com/docview/2844107172
https://search.proquest.com/docview/2842455428
https://pubmed.ncbi.nlm.nih.gov/PMC10363714
Volume 13
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