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Simplifying Correction of Doubly Charged Ion Interferences with Agilent ICP-MS MassHunter

Technical notes | 2019 | Agilent TechnologiesInstrumentation
Software, ICP/MS
Industries
Manufacturer
Agilent Technologies

Summary

Importance of the topic


ICP-MS measurement of trace elements such as Zn, As and Se is routinely challenged by polyatomic and doubly charged ion interferences. Rare earth elements (REEs) and barium in the sample matrix can form M2+ ions that overlap target analyte masses and generate false positives. A streamlined, automated correction for doubly charged ion interferences enhances data quality, reduces method setup time and increases laboratory throughput.

Goals and overview of the study


This study presents an automated M2+ correction routine implemented in Agilent ICP-MS MassHunter software for the 7800 and 7900 platforms. The objectives were to:
  • Develop a direct monitoring approach for REE2+ and Ba2+ interferences on m/z 65–82.
  • Integrate correction equations into routine acquisition via a Method Wizard.
  • Validate accuracy improvements for Zn, As and Se in spiked samples containing high levels of Ba or REEs.

Methodology and instrumentation


Samples of Zn, As and Se standards were spiked with Ba, Nd, Sm, Gd and Dy at varying concentrations (up to 5000 ppb Ba; 50 ppb Nd/Sm; 5 ppb Gd/Dy). Measurements were performed on an Agilent 7800 ICP-MS with helium collision/reaction cell and “narrow peak mode” enabled (peak width ~0.3 u). The software applied +0.5 u mass offsets to monitor half-mass M2+ isotopes (e.g. 67.5, 72.5, 73.5, 77.5, 81.5). Correction equations based on natural isotopic abundance ratios were calculated automatically and applied post-acquisition.

Instrumentation used


  • Agilent 7800 ICP-MS with helium CRC and narrow peak mode
  • ICP-MS MassHunter software v4.5 or later with Advanced Acquisition module
  • Standard sample introduction system and online mixing manifold

Main results and discussion


Automated M2+ correction improved accuracy across all test matrices:
  • Zn recovery remained within ±10% up to 500 ppb Ba; without correction, 5000 ppb Ba caused Zn over-estimation (130% recovery), which was restored to 96% after correction.
  • As spikes with 50 ppb Nd/Sm yielded 148% recovery without correction; automated correction recovered As at 106%.
  • Se measurements in the presence of 5 ppb Gd/Dy showed 215% recovery without correction and 107% after applying M2+ correction.

These results demonstrate the reliability of direct M2+ monitoring and correction equations to compensate for matrix-induced charge state interferences.

Benefits and practical applications of the method


The integrated correction tool:
  • Eliminates complex manual setup of correction equations.
  • Runs in real time during routine sample analysis.
  • Reduces operator workload and risk of human error.
  • Maintains high sample throughput by avoiding additional cell gases.

Future trends and possible applications


Further developments may include:
  • Extension of automated charge state correction to other analyte sets and higher mass ranges.
  • Integration with advanced data processing and machine learning to predict matrix effects.
  • Application in regulatory and environmental monitoring where trace accuracy is critical.
  • Coupling with automated sample introduction systems for high-throughput QA/QC workflows.

Conclusion


The Agilent ICP-MS MassHunter doubly charged ion correction feature provides a robust and user-friendly solution for mitigating M2+ interferences on Zn, As and Se. By automating mass offset monitoring and correction equation application, the tool enhances analytical accuracy and laboratory efficiency without requiring additional reactive gases or lengthy method development.

Reference


Kubota T. Simplifying Correction of Doubly Charged Ion Interferences with Agilent ICP-MS MassHunter; Agilent Technologies, Inc., 2019; Publication 5994-1435EN.

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