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Excessive nitrogen (N) and phosphorus (P) result in serious eutrophication of water. In this study, magnesium modified acid bentonite was prepared by the impregnation method, and nitrogen and phosphorus were simultaneously removed by the magnesium ammonium phosphate method (MAP), which solved the problem of the poor adsorption capacity of bentonite. The morphology and structure of MgO-SBt were characterized by XRD, FT-IR, SEM, EDS, XPS, BET, etc. The results show that the acidified bentonite can increase the distance between bentonite layers, the layer spacing is expanded to 1.560 nm, and the specific surface area is expanded to 95.433 m

With the widespread photovoltaic deployment to achieve the net-zero energy goal, the resulting photovoltaic waste draws attention. In China, considerable steps have not been taken for photovoltaic waste management. The lack of relevant scientific information on photovoltaic waste brings difficulties to the establishment of photovoltaic waste regulatory systems. In this study, the necessity and feasibility of photovoltaic waste recovery were investigated. In China, the photovoltaic waste stream was quantified as 48.67-60.78 million t in 2050. In photovoltaic waste, indium, selenium, cadmium, and gallium were in high risk, judging by the metal criticality analysis, which meant that their recovery was significant to alleviate the resource shortage. The full recovery method was proved to reduce the environmental burdens most. For cost and benefit analysis, the net present value/size was -1.02 $/kg according to the current industrial status. However, it can be profitable with the recovery of silver. This study provides scientific and comprehensive information for photovoltaic waste management in China and is expected to promote the sustainable development of photovoltaic industry.

A water-stable thin film composed of C6H4NH2CuCl2I was fabricated using spin-coating precursor solutions that dissolved equimolar amounts of C6H4NH2I and CuCl2 in N,N-dimethylformamide. Photoelectrochemical characteristics show that the C6H4NH2CuCl2I film demonstrated a stable photocurrent (∼1 μA/cm2) in an aqueous solution under white light (11.5 mW/cm2) even after 3000 s, while exhibiting a photon-to-current efficiency of 0.093% under AM1.5 (100 mW/cm2) illumination. However, these values were significantly lower than those of the CH3NH3PbX3 (X = I, Cl) film in solid devices. The electron diffusion length L(e-) (373 nm) and hole diffusion length L(h+) (177 nm) in the C6H4NH2CuCl2I photoelectrode were significantly lower than those of CH3NH3PbX3, limiting the photoelectrochemical and photocatalysis performances. Moreover, L(h+) was shorter than L(e-) in the C6H4NH2CuCl2I photoelectrode, resulting in the hole-collecting efficiency [ηc(h+)] being lower than the electron-collecting efficiency [ηc(e-)]. A CuO interlayer was introduced as a hole transport layer for the C6H4NH2CuCl2I photoelectrode, which improved L(h+) and ηc(h+).

The dynamic covalent kinetic resolution was efficiently realized for the synthesis of an enantiopure ((R) -5-acetoxy-1,3-oxathiolan-2-yl)ethyl benzoate (PR) from substrates 2-(phenylmethoxy)acetald...

The chemoenzymatic conversion of cyclohexanone to e-caprolactone (1.25 M) mediated by immobilized lipase from T. laibacchi was successfully achieved with a yield of 98.6%, which is much higher than...