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Electrospray Ionization (ESI) Mass Spectrometry01:12

Electrospray Ionization (ESI) Mass Spectrometry

2.6K
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...
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Analyte Adsorption and Distribution01:09

Analyte Adsorption and Distribution

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In certain chromatographic separations, solutes transfer between the mobile phase and the stationary phase via sorption, which typically refers to the process of adsorption. For many chromatographic systems, the sorption process often depends on the polarity of the compounds—an expression of the overall dipole moment within the molecule. During the separation process, there is competition between the solute and solvent for adsorption to the stationary phase. Highly polar compounds and...
3.0K
Inductively Coupled Plasma Atomic Emission Spectroscopy: Principle01:19

Inductively Coupled Plasma Atomic Emission Spectroscopy: Principle

2.2K
Inductively coupled plasma (ICP) is the most widely used plasma source in atomic emission spectroscopy (AES), also known as Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). The ICP source, or torch, consists of three concentric quartz tubes with argon gas flowing through them. A spark from a Tesla coil initiates the ionization of argon, generating a high-temperature plasma.
The ions and electrons produced interact with the fluctuating magnetic field created by a water-cooled...
2.2K
Capillary Electrophoresis: Instrumentation01:20

Capillary Electrophoresis: Instrumentation

1.5K
Capillary electrophoresis instrumentation typically consists of several key components. A high-voltage power supply generates the electric field necessary for the separation by connecting to an anode (the positively charged electrode) and a cathode (the negatively charged electrode) located in buffer reservoirs at each end of the capillary tube. The system includes a sample vial, a fused silica capillary tube coated with polyimide for mechanical strength through which the sample components...
1.5K
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

2.7K
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...
2.7K
Diffusion on Chromatography Columns01:07

Diffusion on Chromatography Columns

1.5K
In column chromatography, when an analyte is introduced as a narrow band at the top of the column, the solutes begin to separate and broaden, developing a Gaussian profile. This broadening occurs due to various factors, such as longitudinal diffusion.
Longitudinal diffusion occurs when the solute molecules in the mobile phase diffuse from the more concentrated center of the chromatographic band to the more dilute regions on either side, both towards and against the flow direction. This...
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Related Experiment Video

Updated: Mar 16, 2026

Characterizing Bacterial Volatiles using Secondary Electrospray Ionization Mass Spectrometry SESI-MS
08:54

Characterizing Bacterial Volatiles using Secondary Electrospray Ionization Mass Spectrometry SESI-MS

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Study on diffusion behavior of analyte in an electrospray ionization source.

Fang Yuan Gao1,2, Ling Yi Zhang1, Xiu Qin Li2

  • 1Shanghai Key Laboratory of Functional Materials Chemistry, East China University of Science and Technology, Shanghai, 200237, China.

Rapid Communications in Mass Spectrometry : RCM
|August 20, 2016
PubMed
Summary

Analyte diffusion in electrospray ionization (ESI) impacts sensitivity. This study compared infusion and flow injection analysis (FIA) modes, revealing distinct diffusion behaviors and providing insights for ESI source design.

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Area of Science:

  • Analytical Chemistry
  • Mass Spectrometry

Background:

  • Analyte diffusion significantly affects sensitivity in electrospray ionization (ESI) sources.
  • Understanding diffusion behavior is crucial for optimizing ESI performance.

Purpose of the Study:

  • To investigate analyte diffusion in ESI without confounding factors.
  • To compare diffusion behavior in different injection modes (infusion vs. FIA).

Main Methods:

  • Utilized model compounds (Chloramphenicol and melamine) and their stable isotope-labeled (SIL) analogs.
  • Compared relative responses in infusion and flow injection analysis (FIA) modes under varying temperatures.
  • Examined different operation modes and ion source configurations.

Main Results:

  • Observed opposite trends in relative responses with temperature changes between infusion and FIA modes.
  • Demonstrated distinct analyte concentration distributions in the two injection modes.
  • Confirmed these differences across various operation modes and ion source types.

Conclusions:

  • Infusion and FIA modes exhibit different analyte diffusion characteristics in ESI.
  • These findings offer a theoretical foundation for ESI source design and mechanism elucidation.
  • Provides a better understanding of electrospray ionization principles.