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Halogens (Cl, Br, and I) are major complexing agents for metal ions, and their ratios (Br/Cl and I/Cl) have been used to determine the source and evolution of hydrothermal fluid. Halogen fractionation during hydrothermal fluid evolution, however, has been inferred from several studies, which poses problems in using halogen ratios as a fluid tracer. The Br/Cl and I/Cl ratios of scapolite are consistent with those ratios present in the coexisting fluid during scapolite formation, making this mineral particularly useful for understanding hydrothermal fluid evolution. To better understand halogen fractionation during vapor-brine phase separation, we conducted fluid inclusion microthermometry, major elements, and in situ halogens and Sr isotope analysis of scapolite formed from a high-salinity hydrothermal fluid during the vapor-brine phase separation at the Yixingzhai gold deposit, North China Craton. The studied scapolite has 1.84–3.41 wt% Cl, 389–806 ppm Br, 8.4–24.4 ppm I, and significantly high Br/Cl (6.1–14.7 × 10–3) and high I/Cl (91–302 × 10–6) molar ratios that likely result from the preferential incorporation of Br and I into the brine phase compared to Cl entering the vapor phase during fluid phase separation. Based on fluid inclusion microthermometry results, the Rayleigh fractionation simulation shows that the Br/Cl and I/Cl ratios of the brine are estimated to be up to 18 × 10–3 and 500 × 10–6 during the formation of scapolite. These results reveal halogen fractionation during the vapor-brine phase separation of hydrothermal fluids. This view has implications for interpreting the halogen systematics of scapolite and other minerals formed in similar environments, particularly when they are used as a fluid tracer. [ABSTRACT FROM AUTHOR]

Water splitting driven by solar energy to produce hydrogen, which is highly dependent on the designing of semiconductor photocatalyst, is an efficient technology to address energy shortage problems and environment issues simultaneously. Here, the halogen and potassium binary-doped graphitic carbon nitride (named as X-K-C 3 N 4 , X = F, Cl, Br, I) photocatalysts were synthetized via simply one pot thermal polymerization method, which shown optimized band structure, enhanced optical absorption, higher separation rate of photogenerated carriers, and thus improved photocatalytic performance under visible light irradiation. As result, F–K–C 3 N 4 is demonstrated to be highly efficient in the separation and transfer of carriers owing to the existence of C–F bond, C N triple bond and K junction. The F–K–C 3 N 4 shows a highest H 2 evolution rate of 1039 μmol g−1 h−1 and a remarkable stability under visible light irradiation (λ ≥ 420 nm), which is about 8.5 times higher than that of pristine g-C 3 N 4. • We systematically studied the effect of K and halogen binary-doped graphitic carbon nitride on photocatalytic performance. • The significantly enhanced photocatalytic activity is described to the double accelerations of F, K binary doping. • F–K–C 3 N 4 exhibits improved visible light harvesting ability and photogenerated charge separation rate. • The F–K–C 3 N 4 exhibits 8.5 times higher H 2 generation rate than that of pristine C 3 N 4. [ABSTRACT FROM AUTHOR]