Spatial-temporal distribution characteristics of surface water pollutants and their potential sources in Ngari, China.

The Ngari region has many important rivers and is critical to water resource security and water resource continuity in China and even in adjoining Asian countries. However, the spatial distribution and monthly variation in local water quality have been poorly understood until recently. In this study, the spatial-temporal variations of 12 water quality parameters, including pH, dissolved oxygen (DO), permanganate index (IMn), chemical oxygen demand (COD), five-day biochemical oxygen demand (BOD5), ammonia nitrogen (NNH3), total nitrogen (Ntotal), total phosphorus (Ptotal), copper (Cu), fluoride (F), arsenic (As) and cadmium (Cd), were determined from samples collected monthly at 22 water cross-sectional sites in the Ngari region in 2020. The surface water pollution in the southern Ngari region was the most serious, and the water pollution level in winter was higher than that in the other seasons. As (0.0781 ~ 0.6154 mg/L) and F (1.05 ~ 4.64 mg/L) were the main exceedance factors derived from the recharge of high arsenic and fluoride geothermal water and weathering of As and F-bearing minerals. The hazard quotient and carcinogenic risk for As and F at the five contaminated sampling sites indicated potential health risks and even carcinogenicity to local populations. The hydrochemistry types of the lakes and rivers in the Ngari region were mainly chloride water and carbonate water. The results from this study can provide a scientific basis for the prevention and control of surface water pollution in the Ngari region and contribute to subsequent research on the ecology of water bodies.

Oxygen vacancy-rich K-Mn3O4@CeO2 catalyst for efficient oxidation degradation of formaldehyde at near room temperature.

Synthesis of catalysts with high catalytic degradation activity for formaldehyde (HCHO) at room temperature is highly desirable for indoor air quality control. Herein, a novel K-Mn3O4@CeO2 catalyst with excellent catalytic oxidation activity toward HCHO at near room temperature was reported. In particular, the K addition in K-Mn3O4@CeO2 considerably enhanced the oxidation activity, and importantly, 99.3 % conversion of 10 mL of a 40 mg/L HCHO solution at 30 °C for 14 h was achieved, with simultaneous strong cycling stability. Moreover, the addition of K species considerably influenced the chemical valence state of Mn from +4 (ε-MnO2) to +8/3 (Mn3O4) on the surface of CeO2, which obviously changed the tunnel structure and the number of oxygen vacancies. One part of K species is uniformly dispersed on K-Mn3O4@CeO2, and the other part exists in the tunnel structure of Mn3O4@CeO2, which is mainly used to balance the negative charge of the tunnel and prevent collapse of the structure, providing enough active sites for the catalytic oxidation of HCHO. We observed a phase transition from tunneled KMnO2 to Mn3O4 to tunneled MnO2 with the decreasing K+ content, in which K-Mn3O4@CeO2 exhibited higher HCHO oxidation activity. In addition, K-Mn3O4@CeO2 exhibited lower oxygen vacancy formation and HCHO adsorption energies in aqueous solution based on density functional theory calculations. This is because the K species provide more active oxygen species and richer oxygen vacancies on the surface of K-Mn3O4@CeO2, promote the mobility of lattice oxygen and the room-temperature reduction properties of oxygen species, and enhance the ability of the catalyst to replenish the consumed oxygen species. Finally, a possible HCHO catalytic oxidation pathway on the surface of K-Mn3O4@CeO2 catalyst is proposed.