Abstract
Particle analysis has benefitted from the advent of single particle inductively coupled plasma-mass spectrometry (spICP-MS) due to its robustness, sensitivity, and high-throughput nature. Previous methods of spICP-MS have typically utilized quadrupole or time-of-flight mass analyzers and therefore employ electron multiplier-based detectors (such as secondary electron multipliers or microchannel plates). However, to obtain precise measurements on elemental or isotopic ratios within individual particles, multi-collector ICP-MS (MC-ICP-MS) can be used. Here, we investigate Ce isotope ratios, specifically 142Ce/140Ce, by spMC-ICP-MS using an all-Faraday cup collector array. Using 1 μm (diameter) cerium dioxide particles, integration times of the Faraday cup detectors were varied from 50-500 ms. The signal from the cerium isotopes in the particles was used to determine isotope ratios, which closely matched the expected natural isotopic abundances. Due to the signal decay response from the Faraday cups, the signal from particles lasts much longer than the expected 1-2 ms (up to 100 s of ms). To explore this effect on isotope ratio analysis, multiple ratio analysis methods were used to determine how to obtain optimal precision and accuracy. Relative differences were around 2% for methods that calculated isotope ratios from summing the total signal of an individual particle before calculating the ratio (rather than using every data point individually). It was found that summing all data points per particle, or integrating under the signal peak, yielded both accurate and precise isotope ratios within the particle population. Particles were also sampled off a solid substrate via microextraction, and isotope ratios were determined with relative differences of 0.13% to 9%. This demonstrates the ability to use spMC-ICP-MS to obtain isotope ratios on particles, with little to no relative difference in comparison to the expected ratio, even when operating Faraday detectors at fast 50 ms integration times.
| Original language | English |
|---|---|
| Pages (from-to) | 1483-1493 |
| Number of pages | 11 |
| Journal | Journal of Analytical Atomic Spectrometry |
| Volume | 40 |
| Issue number | 6 |
| DOIs | |
| State | Published - Apr 24 2025 |
Funding
This work was supported by the Oak Ridge National Laboratory, managed by UT-Battelle for the Department of Energy under contract DE-AC05-000R22725. This work was funded by the United States National Nuclear Security Administration's (NNSA) Office of Defense Nuclear Nonproliferation Research & Development. The authors would like to acknowledge Jacquelyn DeMink at ORNL for assistance with graphic design. We would like to thank Spencer Scott and Rachel Bergin at Savannah River National Laboratory for their support in production of the ceria test particles and Lax Saraf and Kelliann Koehler at the Clemson Electron Microscopy Facility for their help in acquiring the SEM data.