Abstract
A method using multiple-collector inductively coupled plasma source mass spectrometry for the precise measurement of Ti isotope composition in natural materials has been developed. Instrumental mass discrimination is corrected using a "standard-sample bracketing" approach by expressing the isotope ratios of samples relative to those of the bracketing standard. Variations in 47Ti/46Ti, 48Ti/46Ti, 49Ti/46Ti and 50Ti/46Ti ratios of samples are expressed in ε units which are deviations in parts per 104 from the same isotope ratios of the reference material. The long-term repeatability at the 2 standard deviation level is 0.4, 0.6, 0.7 and 0.8 ε units in terms of 47Ti/46Ti, 48Ti/46Ti, 49Ti/46Ti and 50Ti/46Ti ratio measurements, respectively. The technique reported here makes it possible for the first time that both mass-dependent fractionation and isotope anomalies of Ti isotopes in natural materials can be measured to high precision.
Original language | English |
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Pages (from-to) | 21-29 |
Number of pages | 9 |
Journal | International Journal of Mass Spectrometry |
Volume | 220 |
Issue number | 1 |
DOIs | |
Publication status | Published - Sept 15 2002 |
Keywords
- Matrix effects
- Plasma source mass spectrometry
- Stable isotopes
- Titanium isotopes
- Transition metal
ASJC Scopus subject areas
- Instrumentation
- Condensed Matter Physics
- Spectroscopy
- Physical and Theoretical Chemistry