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Related Concept Videos

Tandem Mass Spectrometry01:21

Tandem Mass Spectrometry

Tandem mass spectrometry is a technique that uses multiple mass analyzers in series to obtain a higher selectivity and reduce chemical noise during analyte detection. Instruments with multiple analyzers separated by an interaction cell enable secondary fragmentation and selected study of the fragment ions.Secondary fragmentations occur in the interaction cell and can be induced by various factors. Fragmentation induced by collision with inert gases, such as N2, Ar, He, etc., is called...
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...
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...
¹³C NMR: ¹H–¹³C Decoupling01:04

¹³C NMR: ¹H–¹³C Decoupling

The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
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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...
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Inductively Coupled Plasma–Mass Spectrometry (ICP–MS): Overview

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Related Experiment Video

Updated: May 8, 2026

Preparing an Isotopically Pure 229Th Ion Beam for Studies of 229mTh
10:42

Preparing an Isotopically Pure 229Th Ion Beam for Studies of 229mTh

Published on: May 3, 2019

Carbon ion stripper for NSTRI tandem accelerator.

M Mohseni Kejani1,2, F Ghasemi3, F Abbasi Davani1

  • 1Department of Radiation Application, Faculty of Nuclear Engineering, Shahid Beheshti University, P.O. Box 19839-69411, Tehran, Iran.

Scientific Reports
|May 6, 2026
PubMed
Summary

Researchers optimized a stripper section for a carbon ion beam accelerator, achieving efficient charge exchange for Accelerator Mass Spectrometry (AMS). This design enhances radiocarbon dating accuracy by improving isotopic discrimination in carbon measurements.

Keywords:
charge exchange interactionequilibrium thicknessgas stripperradiocarbon datingtandem technique

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Using a Cyclic Ion Mobility Spectrometer for Tandem Ion Mobility Experiments
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Last Updated: May 8, 2026

Preparing an Isotopically Pure 229Th Ion Beam for Studies of 229mTh
10:42

Preparing an Isotopically Pure 229Th Ion Beam for Studies of 229mTh

Published on: May 3, 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

Area of Science:

  • Nuclear Physics and Engineering
  • Accelerator Science and Technology
  • Analytical Chemistry

Background:

  • The Nuclear Science and Technology Research Institute (NSTRI) is developing a 1.7 MV tandem accelerator for Accelerator Mass Spectrometry (AMS).
  • A critical component for AMS is the stripper section, responsible for optimizing ion charge states.
  • This study focuses on the design of a stripper section specifically for carbon ion beams.

Purpose of the Study:

  • To design and optimize a stripper section for a carbon ion beam within a 1.7 MV tandem accelerator.
  • To achieve efficient charge exchange and equilibrium thickness for various carbon charge states.
  • To validate the design through simulations and experimental measurements, considering isotopic mass effects.

Main Methods:

  • Derived interaction cross-sections for 14 charge state transitions ((q, q+1) and (q, q-1)).
  • Introduced an optimal geometry and calculated charge exchange efficiency based on gas throughput.
  • Validated simulation results with experimental pressure measurements and compared charge-state fractions with existing data.

Main Results:

  • Achieved an equilibrium thickness of 2.3 × 1016 cm-2 at 9 SCCM gas throughput.
  • Reported 14C/12C stripping ratios of 1.22, 1.01, and 0.89 for charge states 1+, 2+, and 3+ respectively.
  • Demonstrated close agreement between simulated and experimental results, validating the optimized stripper design.

Conclusions:

  • The optimized stripper section geometry ensures efficient charge exchange equilibrium for carbon ions.
  • The design accounts for isotopic mass effects, crucial for accurate AMS-based radiocarbon measurements.
  • The compact design reduces overall length by approximately two-thirds compared to conventional strippers, enhancing practicality.