Fast and precise boron isotopic analysis of carbonates and seawater using Nu Plasma II multi‐collector inductively coupled plasma mass spectrometry and a simple sample introduction system
Rationale The boron (B) isotopic composition in marine carbonates provides important insights into paleoclimate reconstruction and biomineralization. However, precise and accurate measurements of B isotopes using plasma‐based mass spectrometry is difficult due to the volatile nature of B, which typi...
Gespeichert in:
Veröffentlicht in: | Rapid communications in mass spectrometry 2019-07, Vol.33 (14), p.1169-1178 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Rationale
The boron (B) isotopic composition in marine carbonates provides important insights into paleoclimate reconstruction and biomineralization. However, precise and accurate measurements of B isotopes using plasma‐based mass spectrometry is difficult due to the volatile nature of B, which typically requires complex and more specialized sample introduction systems. Existing analytical protocols have mostly been based on Thermo Scientific Neptune Plus multi‐collector inductively coupled plasma mass spectrometry (MC‐ICPMS) instruments, whereas methods based on Nu Plasma mass spectrometers are scarce.
Methods
We have developed a simplified analytical protocol using Nu Plasma II MC‐ICPMS with standard glass sample introduction systems. Boron extraction and purification were conducted using a two‐stage column chemistry with cation‐exchange and Amberlite IRA 743 B‐specific resin. A sample drying step was avoided, which allows for direct isotopic analysis after column chemistry. A wet plasma mode with a standard glass cyclonic spray chamber and a glass nebulizer was used instead of a more specialized perfluoroalkoxy (PFA) sample introduction system. Low residual B signals were achieved with a relatively short period of wash‐out with 0.5 N HNO3.
Results
The external precision is better than 0.30‰ (2SD) calculated from the long‐term bracketing standard, NIST SRM 951a. The overall robustness of the method was demonstrated by measurements of the international carbonate standard JCp‐1 (δ11B = +24.49 ± 0.36‰, 2SD) and seawater (δ11B = +39.98 ± 0.35‰), which are consistent with reported values.
Conclusions
Our method provides an alternative approach for B isotope analysis using a routine wet plasma MC‐ICPMS setup that can facilitate geochemical and environmental application of B isotopes. |
---|---|
ISSN: | 0951-4198 1097-0231 |
DOI: | 10.1002/rcm.8456 |