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Synthesis of molybdenite reference materials for in situ molybdenum and sulfur isotope measurement using laser ablation MC-ICP-MS.

Authors :
Jing Tian
Zhian Bao
Kaiyun Chen
Nan Lv
Wenqiang Yang
Xiaojuan Nie
Honglin Yuan
Source :
JAAS (Journal of Analytical Atomic Spectrometry). Jun2024, Vol. 39 Issue 6, p1503-1513. 11p.
Publication Year :
2024

Abstract

Analyzing sulfur (S) and molybdenum (Mo) isotope ratios in molybdenite, the most common sulfide mineral, is crucial for studying the genesis of ore deposits. However, it is necessary to prepare matrix-matched reference materials for molybdenite. In this study, we employed two different techniques, the high-temperature-high-pressure (HTHP) technique and the rapid hot-pressing technique, to synthesize molybdenites and assessed their suitability as reference materials for in situ Mo and S isotope analysis in molybdenite. The molybdenites synthesized through HTHP and rapid hot-pressing exhibit smooth surfaces and dense structures, making them suitable as reference materials for in situ Mo and S isotope analysis, respectively. These synthesized molybdenites exhibit homogeneous Mo and S isotope compositions based on a large number of LA-MC-ICP-MS measurements. The mean δ98MoNIST SRM 3134 values of 0.70 ± 0.06‰ (n = 4, 2SD) and 0.70 ± 0.05‰ (n = 4, 2SD) determined by solution nebulization MC-ICP-MS are suggested as recommended δ98Mo/95Mo values for Mo-H8 and Mo-P. The mean δ34SV-CDT value of −0.22 ± 0.10‰ (n = 9, 2SD) determined by elemental analyzer isotope ratio mass spectrometry (EA-IRMS) is suggested as a recommended δ34S/32S value for Mo-H8 and Mo-P. Therefore, we recommend combining ultrafine powders with a high-temperature–high-pressure technique and/or a rapid hot-pressing technique to synthesize reference materials for isotopic analysis of other minerals. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02679477
Volume :
39
Issue :
6
Database :
Academic Search Index
Journal :
JAAS (Journal of Analytical Atomic Spectrometry)
Publication Type :
Academic Journal
Accession number :
177683654
Full Text :
https://doi.org/10.1039/d4ja00008k