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Related Concept Videos

Controlled-Potential Coulometry: Electrolytic Methods01:17

Controlled-Potential Coulometry: Electrolytic Methods

Controlled-potential coulometry, also known as potentiostatic coulometry, employs a three-electrode system in which the working electrode's potential is precisely regulated using a potentiostat. Platinum working electrodes are utilized for positive potentials, while mercury pool electrodes are favored for extremely negative potentials. The platinum counter electrode is separated from the analyte using a membrane or salt bridge to avoid interference in the analysis.
The chosen potential ensures...
Voltammetry: Factors Affecting Measurements01:21

Voltammetry: Factors Affecting Measurements

A current produced due to the redox reactions of the analyte at the working and auxiliary electrodes is called a faradaic current. The reaction can be divided into two types. The current generated due to the reduction of the analyte is called cathodic current, and it carries a positive charge. In contrast, the current produced by analyte oxidation is known as an anodic current, and it has a negative charge. The applied potential at the working electrode determines the faradaic current flow, and...
Voltammetry: Overview01:20

Voltammetry: Overview

Voltammetry is an electroanalytical technique in which the current flowing through an electrochemical cell is measured as a function of applied potential, typically under conditions of concentration polarization. The technique provides valuable information about redox-active species, and the current response is plotted as a voltammogram.
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The Electrical Double Layer01:30

The Electrical Double Layer

In the region where two bulk phases meet, an intricate electric charge distribution arises due to charge transfer, ion adsorption, molecular orientation, and charge distortion. This complex distribution is commonly referred to as the electrical double layer.When a solid electrode interfaces with ions in an electrolyte solution, the speed of electron transfer dictates the rates of oxidation and reduction. The electrode acquires a charge through the escape of atoms into the solution as cations or...
Processes at Electrodes01:30

Processes at Electrodes

The electrode interacts with ions in the electrolyte solution at its interface. The rate of oxidation and reduction depends on the speed at which electrons can transfer through this interface. As ions attach to or leave the electrode surface, the electrode acquires a charge, and an electrical potential forms across the interface, making the process more difficult to reach equilibrium. The charge on the electrode affects the local ion concentrations in the solution, though thermal motion...
Potentiometry: Membrane Electrodes01:15

Potentiometry: Membrane Electrodes

Membrane electrodes, also known as p-ion electrodes, use membranes that selectively interact with free analyte ions, generating a potential difference across the membrane. The resulting membrane potential, known as the asymmetry potential, is not zero even when analyte concentrations on both sides of the membrane are equal. The membrane's response is typically not selective to a single analyte but proportional to the concentration of all ions in the sample solution capable of interacting at the...

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Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone
08:06

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Published on: February 23, 2017

Bipolar electrode focusing: faradaic ion concentration polarization.

Robbyn K Anand1, Eoin Sheridan, Kyle N Knust

  • 1Department of Chemistry and Biochemistry, Center for Electrochemistry, University of Texas at Austin, 1 University Station, A5300, Austin, Texas 78712-0165, United States.

Analytical Chemistry
|March 1, 2011
PubMed
Summary

This study introduces a novel bipolar electrode (BPE) device for highly efficient analyte concentration. The microfluidic system achieves up to 500,000-fold enrichment of charged molecules, simplifying complex analyses.

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Area of Science:

  • Electrochemistry
  • Microfluidics
  • Analytical Chemistry

Background:

  • Bipolar electrodes (BPEs) create electric field gradients.
  • Ion depletion and enrichment zones are formed at BPE boundaries.
  • Microfluidic devices enable precise control over chemical processes.

Purpose of the Study:

  • To demonstrate significant concentration enrichment of charged analytes using a BPE.
  • To investigate the efficiency of a dual-channel microfluidic configuration with a BPE.
  • To present a simpler and more flexible alternative to existing ion concentration polarization methods.

Main Methods:

  • Utilizing a bipolar electrode (BPE) within a dual-channel microfluidic setup.
  • Generating an electric field gradient opposing a counter-flow to enrich analytes.
  • Employing Faradaic reactions at the BPE ends to create ion depletion/enrichment zones.

Main Results:

  • Achieved concentration enrichment of a fluorescent tracer by up to 500,000-fold.
  • Demonstrated enhanced enrichment rates (up to 71-fold/s) using the dual-channel configuration.
  • The BPE microfluidic device proved experimentally flexible and simple to construct.

Conclusions:

  • Bipolar electrode technology offers a powerful method for analyte preconcentration.
  • The dual-channel microfluidic system significantly boosts enrichment efficiency.
  • This approach provides a simplified and versatile platform for micro/nanochannel junction applications.