A. Galy et al., High-precision measurement of magnesium isotopes by multiple-collector inductively coupled plasma mass spectrometry, INT J MASS, 208(1-3), 2001, pp. 89-98
Multiple-collector inductively coupled plasma mass spectrometry has been us
ed for the precise measurement of variations in the isotopic composition of
Mg in a range of materials. The contributions of C-C, C-N, and Mg-H molecu
lar species to the mass spectrum in the Mg mass region are minimised. Varia
tions in sample Mg-26/Mg-24 and Mg-25/Mg-24 ratios are expressed as delta M
g-26 and delta Mg-25 units, which are deviations in parts per 10(3) from th
e same ratio in the SRM 980 Mg standard. The long-term repeatability of the
Mg-26/Mg-24 and Mg-25/Mg-24 ratios of a sample Mg solution relative to the
SRM 980 Mg isotope standard are 0.12 parts per thousand, and 0.06 parts pe
r thousand, respectively, at 95% confidence. The addition of Na, Al, and Ca
in a solution of Mg having a known isotopic composition induces 0.2 parts
per thousand -1 parts per thousand increase of delta Mg-26. This chemical b
ias is a result of a mass-dependent process and is observed to be greater w
ith Ca than Na. Isobaric interference from doubly charged Ca-48 ions on mas
s 24 is observed to be significant when [Ca]/[Mg] greater than or equal to
0.5. The results obtained on nine terrestrial material show a variation of
Mg-isotopes of 4 parts per thousand in delta Mg-26. When plotted in a three
-isotope diagram, all the data fall on a single mass fractionation line. Th
e excess of Mg-26 has been determined by the deviation from that mass-depen
dent relationship, and its long-term repeatability is 0.06 parts per thousa
nd at 95% confidence. (C) 2001 Elsevier Science B.V.