This study proposes new data on the rare pyroxene, variety violane, sampled from itstype locality, Praborna manganese deposit, near Saint Marcel (Val d'Aosta, Italy). Violane is veryappreciated as a gemstone for its different hues of violet-blue color and is characterized by its diop-sidic or omphacitic composition. To assess the possible causes of color, electron-probe microanalysis(EMPA) and laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) were usedto establish the chemical composition. Raman and Fourier transform infrared (FTIR) spectroscopy,ideal for the non-destructive analysis, identified the different present phases directly on gemstone.Raman and FTIR spectra highlighted the presence, in the same sample, of diopside and omphaciteshowing almost inappreciable violet hue difference. The two minerals were easily differentiated bymicroprobe analyses and showed a compositional heterogeneity not linked to the different colors.The best way to detect the color-causing elements in microcrystalline violanes resulted in the analysisof trace elements and their quantification. An enrichment of Ti and Li characterizes darker violetomphacite and that of V and rare-earth elements (REE) the lilac-lavender or light violet-blue diopside.In general, our results led us to say that the color changes, previously proposed as due to Mn bothin divalent and trivalent oxidation state, may be controlled by trace elements or by concentrationof minor elements, such as Fe, and their oxidation state. REE patterns showed a negative anomalyof Ce that could be ascribed to the variation of the oxygen chemical potential occurring in the ore.The new data, combined with previous results, may provide new constrains on the processes thatgenerated the Mn-rich deposit of Praborna.

New Insights for Gem-Quality Mn-Bearing Diopside-Omphacite, Violane Variety, from Saint Marcel (Val D'Aosta, Italy): Its Trace Elements and Spectroscopic Characterization

Diella V;
2021

Abstract

This study proposes new data on the rare pyroxene, variety violane, sampled from itstype locality, Praborna manganese deposit, near Saint Marcel (Val d'Aosta, Italy). Violane is veryappreciated as a gemstone for its different hues of violet-blue color and is characterized by its diop-sidic or omphacitic composition. To assess the possible causes of color, electron-probe microanalysis(EMPA) and laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) were usedto establish the chemical composition. Raman and Fourier transform infrared (FTIR) spectroscopy,ideal for the non-destructive analysis, identified the different present phases directly on gemstone.Raman and FTIR spectra highlighted the presence, in the same sample, of diopside and omphaciteshowing almost inappreciable violet hue difference. The two minerals were easily differentiated bymicroprobe analyses and showed a compositional heterogeneity not linked to the different colors.The best way to detect the color-causing elements in microcrystalline violanes resulted in the analysisof trace elements and their quantification. An enrichment of Ti and Li characterizes darker violetomphacite and that of V and rare-earth elements (REE) the lilac-lavender or light violet-blue diopside.In general, our results led us to say that the color changes, previously proposed as due to Mn bothin divalent and trivalent oxidation state, may be controlled by trace elements or by concentrationof minor elements, such as Fe, and their oxidation state. REE patterns showed a negative anomalyof Ce that could be ascribed to the variation of the oxygen chemical potential occurring in the ore.The new data, combined with previous results, may provide new constrains on the processes thatgenerated the Mn-rich deposit of Praborna.
2021
Istituto di Geologia Ambientale e Geoingegneria - IGAG
Istituto di Geoscienze e Georisorse - IGG - Sede Pisa
Istituto di Scienze del Patrimonio Culturale - ISPC
Istituto di Scienze Polari - ISP
violane-pyroxene
gemology
Val d'Aosta
Western Alps
Italy
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/428547
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