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Ce3+-doped lithium alumino-silicate (Li-Al-Si) scintillating glass was prepared using a melting method and crystallized via heat treatment. X-ray diffraction and transmission electron microscopy confirmed the presence of nanocrystals in the materials. Radioluminescence spectra, obtained by X-ray excitation, and luminescence spectra, obtained by 338 nm excitation, showed that the luminescence intensity increased after crystallization. The glass was combined with pure silica as the inner cladding to fabricate a hybrid fiber core using a melt-in-tube technique. The composition of the fiber core was examined using an electron probe microanalyzer. The glass fiber produced strong blue luminescence under UV excitation. After a micro-crystallizing heat treatment of the hybrid fiber at 850 °C in a reducing atmosphere, a Ce3+-doped lithium alumino-silicate glass–ceramic scintillating hybrid fiber was obtained. The nanocrystal structure of the fiber core was examined using micro-Raman spectroscopy. Excitation and luminescence spectra of the hybrid fiber before and after micro-crystallization were measured using microspectrofluorimetry. The results demonstrated that the fiber remained luminous after micro-crystallization. Hence, this work provides a new way to prepare scintillating glass–ceramic hybrid fibers for neutron detection. [ABSTRACT FROM AUTHOR]

Trace/minor element variation in pyrite is a feature that has proved invaluable for reconstructing a wide range of geological processes. Routine reflectance observations commonly fail to constrain this variation due to the typically subtle and barely perceptible change in reflectance brought about by deviation from ideal stoichiometry. Such differences may be difficult or impossible to observe in conventional polished sections using standard optical microscopes, at least without oil immersion. Chemical etching and staining, although widely used, are destructive, hazardous, or both, and the etching process is not completely reproducible. Here we use the γ correction method to enhance optical digital signal differences obtained in reflected light to constrain compositional heterogeneity in pyrite from a representative hydrothermal ore deposit in eastern China. The γ-enhanced images show significant reflectance variation caused by compositional heterogeneity, confirmed by quantitative electron microprobe analysis and qualitative imaging. Higher reflectance domains in γ-enhanced images correspond to increases in the effective number of free electrons, whereas darker domains are attributed to the decrease of these free electrons by trace/minor element substitution in pyrite (e.g., As). Gamma correction provides a rapid, effective, non-destructive method to constrain compositional heterogeneity of pyrite through enhancement of reflectance variation. Used alone, this method is unable to determine the chemical composition due to simultaneous substitutions, causing a disparate increase or decrease of reflectance, in most ore minerals. Nevertheless, γ correction may be sufficient to predict the substitution of trace/minor elements under the optical microscope prior to scanning electron microscope imaging and quantitative investigation of mineral composition and may help constrain links between textures and compositions of pyrite in evolving ore systems, which could also be applied to other ore minerals with negligible bireflectance. [ABSTRACT FROM AUTHOR]