https://www.selleckchem.com/products/bardoxolone.html In detail, the photocatalytic degradation of Rhodamine B (RhB) activated by visible light using 15% SnO2/Bi2S3-Bi25 shows the efficiency of 80.8%, which is superior compared to that of pure Bi2S3 (29.4%) and SnO2 (0.1%). The SnO2/Bi2S3-Bi25 composite photocatalyst also presents an excellent photostability and easy recovery from dye for recycling. The trapping test revealed that the photogenerated holes play a crucial factor during the photocatalytic process, whereas superoxide radicals are also formed but not involved in the photocatalytic process. Successful fabrication of SnO2/Bi2S3-Bi25 composite photocatalysts via a straightforward method with drastically enhanced photocatalytic performance under visible light activation would be useful for practical applications.Effectively reducing the concentration of CO2 in ambient air is essential to mitigate global warming. Existing carbon capture and storage technology can only slow down the carbon emissions of large point sources but cannot treat the already accumulated CO2 in the environment. Herein, we demonstrated a simple direct CO2 capture method from air via reactive crystallization with a new trichelating iminoguanidine ligand (BTIG). It could strongly bind CO2 to form insoluble carbonate crystals that could be easily isolated. In the crystal, CO2 was transformed to CO32- and trapped in a dense hydrogen bonding network in terms of carbonate-water clusters. This capture process was reversible, and the BTIG ligand could be regenerated by heating the BTIG-CO2 crystal at a mild temperature, which was much lower than the decomposition temperature of CaCO3 (∼900 °C). Thermodynamic and kinetics analyses indicate that the crystallization process was exothermic with an enthalpy of -292 kJ/mol, and the decomposition energy consumption was 169 kJ per mol CO2. In addition, BTIG could also be employed for CO2 capture from flue gas with a capacity of 1.46 mol/mol, which was