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Related Concept Videos

Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Inductively Coupled Plasma-Mass Spectrometry (ICP-MS): Interferences01:20

Inductively Coupled Plasma-Mass Spectrometry (ICP-MS): Interferences

Inductively coupled plasma–mass spectrometry (ICP–MS) is a highly selective and sensitive technique for accurate elemental analysis. Though the analysis of ICP–MS mass spectra is comparatively straightforward, it is affected by spectroscopic and non-spectroscopic interferences. Spectroscopic interferences arise when the plasma contains ionic species with an m/z value the same as the analyte ion. Spectroscopic interference can be categorized as isobaric, polyatomic ions, and refractory oxide ion...
Chemical Ionization (CI) Mass Spectrometry01:21

Chemical Ionization (CI) Mass Spectrometry

The molecular ion peak of a molecule in the mass spectrum provides vital information for molecular identification. However, conventional electron impact ionization can lead to the rapid dissociation of some molecular ions before they reach the detector. A milder ionization method is required to increase the lifetime of such ionized analyte molecules. Chemical ionization (CI) is a gas-phase protonation reaction useful for mass-analyzing analyte molecules that are easily protonated to yield the...
Electrospray Ionization (ESI) Mass Spectrometry01:12

Electrospray Ionization (ESI) Mass Spectrometry

Higher molecular weight biomolecules are nonvolatile compounds that may decompose before ionizing or vaporizing during mass analysis with conventional electron impact ionization methods. Accordingly, electrospray ionization (ESI) is the favored method for vaporizing and ionizing biomolecules as it circumvents rapid fragmentation and enables the recording of mass signals for the entire biomolecule.
ESI utilizes electrical energy to transfer ions from the liquid phase of the sample into the...
Mass Analyzers: Common Types01:19

Mass Analyzers: Common Types

The quadrupole mass analyzer consists of four cylindrical metal rods arranged in a diamond carrying a DC voltage and a radio-frequency AC voltage. The motion of ions through the quadrupole depends on the field strength, causing only ions of a certain m/z to resonate successfully and strike the detector at a given field strength. Though the transmission rate for these analyzers is high, the exact elemental composition of the sample is not determined because of low resolution; however, they are...

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Related Experiment Video

Updated: Jun 15, 2026

Ion Exchange Chromatography (IEX) Coupled to Multi-angle Light Scattering (MALS) for Protein Separation and Characterization
10:41

Ion Exchange Chromatography (IEX) Coupled to Multi-angle Light Scattering (MALS) for Protein Separation and Characterization

Published on: April 5, 2019

Index variation from field-assisted ion exchange.

A R Cooper, M A El-Leil

    Applied Optics
    |March 12, 2010
    PubMed
    Summary

    Unidirectional electric fields combined with diffusion create moving ion distributions in slabs and cylinders. The field direction determines if distributions are stationary or never reach a steady state, impacting optical material production.

    Area of Science:

    • Physics
    • Materials Science

    Background:

    • Understanding ion behavior under combined electric fields and diffusion is crucial for developing advanced materials.
    • Previous models often simplified the interplay between electric fields and diffusion processes.

    Purpose of the Study:

    • To investigate concentration distributions of ions under combined electric fields and diffusion in different geometries.
    • To analyze the impact of electric field direction on ion distribution dynamics.
    • To explore the implications for producing graded-index optical materials.

    Main Methods:

    • Mathematical modeling of ion transport.
    • Analysis of concentration distributions in slab and hollow cylinder geometries.
    • Simulation of ion behavior under unidirectional electric fields and diffusion.

    More Related Videos

    Using a Cyclic Ion Mobility Spectrometer for Tandem Ion Mobility Experiments
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    Using a Cyclic Ion Mobility Spectrometer for Tandem Ion Mobility Experiments

    Published on: January 20, 2022

    Online Size-exclusion and Ion-exchange Chromatography on a SAXS Beamline
    11:09

    Online Size-exclusion and Ion-exchange Chromatography on a SAXS Beamline

    Published on: January 5, 2017

    Related Experiment Videos

    Last Updated: Jun 15, 2026

    Ion Exchange Chromatography (IEX) Coupled to Multi-angle Light Scattering (MALS) for Protein Separation and Characterization
    10:41

    Ion Exchange Chromatography (IEX) Coupled to Multi-angle Light Scattering (MALS) for Protein Separation and Characterization

    Published on: April 5, 2019

    Using a Cyclic Ion Mobility Spectrometer for Tandem Ion Mobility Experiments
    08:40

    Using a Cyclic Ion Mobility Spectrometer for Tandem Ion Mobility Experiments

    Published on: January 20, 2022

    Online Size-exclusion and Ion-exchange Chromatography on a SAXS Beamline
    11:09

    Online Size-exclusion and Ion-exchange Chromatography on a SAXS Beamline

    Published on: January 5, 2017

    Main Results:

    • A unidirectional electric field, aligned with ion velocity, produces stationary, self-similar concentration distributions moving at constant velocity.
    • An opposing electric field leads to ion mixing and distributions that do not reach a steady state.
    • The direction of the electric field is a critical factor in determining the final ion concentration profile.

    Conclusions:

    • The study provides insights into controlling ion distributions for material fabrication.
    • The findings are directly applicable to the production of graded-index optical materials.
    • Tailoring electric field conditions allows for precise control over material properties.