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High spatial resolution multiple sulfur isotope studies undertaken by multi‐collector secondary ion mass spectrometry (SIMS) commonly use well‐characterised sulfide reference materials that do not (or are assumed not to) exhibit mass‐independent fractionation in 33S and 36S, taking advantage of the three‐isotope plot to evaluate the extent of such fractionation in unknown targets. As a result, few studies to date have used a mass independently fractionated reference sulfide to demonstrate accuracy of measurement and/or data reduction procedures. This article evaluates two mass independently fractionated sulfides, a pyrite from the 3.7 Ga Isua greenstone belt and a pyrrhotite from a 2.7 Ga gold deposit in Minas Gerais, Brazil, which may be used to provide additional confidence in the obtained multiple sulfur isotope data. Additionally, the article presents a method for measuring quadruple sulfur isotopes by SIMS at a comparable spatial and volume resolution to that typically employed for triple sulfur isotopes. This method has been applied to the Isua pyrite as well as to a sample of 2.5 Ga pyrite from the Campbellrand, Transvaal, South Africa, previously investigated using SIMS for triple sulfur isotopes, illustrating its potential for quadruple sulfur investigations.  相似文献   
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Multi-Collector SIMS Determination of Trace Lanthanides in Zircon   总被引:3,自引:1,他引:3  
A method is presented for the determination of rare earth elements (REE) in zircon (ZrSiO4) using a multi-collector equipped ion-microprobe operating at moderately high mass resolution (M/ΔM ˜ 3900). The low abundance light REE (La-Eu) were measured simultaneously in six ion counting electron multipliers, reducing analytical time to less than half of that in a monocollection routine. Effective mass filtering, moderate energy filtering and careful set up of detector parameters in order to minimise background counts, yielded a highly coherent set of analyses from the 91500 zircon reference sample.  相似文献   
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