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Geology topics

Edward P. Vicenzi

Publications and source records attributed to Edward P. Vicenzi.

2 recordsLinked to original sources

Correlating quantified cathodoluminescence spectra in jadeite with micro-scale color measurements in visible-near infrared reflectance spectrometry

Cultures throughout history have valued jadeite jade (hereinafter jade), a natural material assemblage composed predominately of the NaAl endmember pyroxene, jadeite (NaAlSi 2 O 6 ) that is prized for its mechanical properties and enticing coloration [ 1 , 2 ]. The geological setting for the formation of jadeite-rich rocks and associated complex geochemical phenomena is well documented in the literature [ 3-5 ]. Unlike single crystal gems, jade often contains a mixture of colors, but the stone is perhaps best known for exhibiting a range of green hues from pale green to blue green, and to deep green [ 1 , 6 ]. Efforts to classify jade color include qualitative matching to a set of reference color tiles, and less commonly, use of a more quantitative set of color perception values first established by International Commission on Illumination’s (CIE 1931) color space, which includes values for light-dark luminance level (L*), a green-red vector (a*), and a blue-yellow vector (b*) [ 7 , 8 ]. Two principal mechanisms have been identified as the cause of green coloration in jadeite: 1) the chemical state of impurity Fe, either 2+ or 3+, and 2) minor to trace Cr in the crystal structure [ 9 , 10 ]. Previous studies have associated Cr 3+ with cathodoluminescence (CL) spectral features in jadeite using point spectrometry, with more recent connections made via 2D CL spectrum imaging [ 11-13 ]. In this effort, we are seeking to establish whether Cr impurities are correlated with green coloration in jadeite using micro-scale (≤110 μm) visible-near infrared (VIS-NIR) reflectance spectrometry.

Microscopy and Microanalysis

Cathodoluminescence imaging and spectrometry of a jadeite microbeam reference crystal: Detection of Ce3+

Options for selecting a high Na concentration mineral for instrument calibration that are suitably stable under the electron beam are limited [ 1 ]. NaCl (approximately a mass fraction of 39 % Na) is not practical for use alongside other embedded and polished materials in a mounted block of standards. While albite (NaAlSi 3 O 8 ; approximately a mass fraction of 8 % Na) represents a typical choice for some microanalysts, it may be subject to time dependent signal intensity issues, such as those observed for Na and other cations during analysis of hydrous glasses [ 2 ]. Near endmember jadeite pyroxene (NaAlSi 2 O 6 ; approximately mass fraction of 11 % Na) represents a desirable option for calibration given its relatively large concentration of Na and insensitivity to electron beam radiation with respect to X-ray output. Despite these desirable characteristics, jadeites have been shown to contain complex microstructures as the result of intracrystalline zoning [ 3 , 4 ], and the impact of chemical inhomogeneity within mineral standards and natural glasses has been documented [ 5-7 ]. In this study, a commercially obtained jadeite crystal (source location “China”) was studied to assess its microscale uniformity using a suite of microbeam methods, including dispersive red-green-blue multispectral cathodoluminescence imaging (CL RGB ), hyperspectral CL imaging spectrometry, energy dispersive X-ray spectrometry (EDS), SEM-based micro-X-ray fluorescence (μXRF), and wavelength dispersive X-ray spectrometry (WDS).

Microscopy and Microanalysis