Issue 8, 2012

Investigation of natural isotopic variation of Sb in stibnite ores via multi-collector ICP-mass spectrometry – perspectives for Sb isotopic analysis of Roman glass

Abstract

Natural variation in the isotopic composition of Sb in stibnites (Sb ores) was explored using multi-collector ICP-mass spectrometry (MC-ICP-MS). A method for isolating Sb (after acid digestion) without introducing artificial mass fractionation was developed, based on the use of a combination of cation exchange chromatography using Dowex AG50-X8 resin and anion exchange chromatography using Amberlite IRA 743 resin. For pure stibnites (Sb2S3), Sb isolation is not strictly required as at a 2 : 3 Sb : S molar ratio, it was demonstrated that the concomitant S does not affect the 123Sb/121Sb isotope ratio result. However, the method can be deployed for other Sb ore types with a lower Sb : S ratio and for samples with lower purity. Indium was used as an internal standard for correction of the instrument-induced mass discrimination occurring in the MC-ICP-MS instrument. The 123Sb/121Sb ratio could be measured with 0.002% repeatability (internal precision), while for the samples the 123ε values were characterized by an uncertainty of 1 ε unit. The isotopic composition of the selected materials (stibnites from various regions of the world) shows a variation spanning 10 ε units (or 0.1%). The method developed shows potential to be used in provenance determination studies of ancient glass.

Graphical abstract: Investigation of natural isotopic variation of Sb in stibnite ores via multi-collector ICP-mass spectrometry – perspectives for Sb isotopic analysis of Roman glass

Supplementary files

Article information

Article type
Paper
Submitted
21 Feb 2012
Accepted
19 Jun 2012
First published
09 Jul 2012

J. Anal. At. Spectrom., 2012,27, 1304-1310

Investigation of natural isotopic variation of Sb in stibnite ores via multi-collector ICP-mass spectrometry – perspectives for Sb isotopic analysis of Roman glass

L. Lobo, V. Devulder, P. Degryse and F. Vanhaecke, J. Anal. At. Spectrom., 2012, 27, 1304 DOI: 10.1039/C2JA30062A

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