After washing and curing, P is transported from the phosphogypsum to the leachate during the phosphogypsum detoxification process, providing two ideas for phosphorus recovery from phosphogypsum leachate: 1) preparatio...After washing and curing, P is transported from the phosphogypsum to the leachate during the phosphogypsum detoxification process, providing two ideas for phosphorus recovery from phosphogypsum leachate: 1) preparation of calcium hydrogen phosphate for feed;2) preparation of calcium phosphate. A ready-to-use calcium oxide slurry was used to recover P from phosphogypsum leachate at a slurry concentration of 20% and a quantitative link between calcium to phosphorus ratio and fixation rate was fitted by mixed use batch experiments, reaction kinetics and thermodynamics, and theoretical calculations were used to demonstrate that phosphorus cannot be completely reused in the preparation of calcium hydrogen phosphate. The findings demonstrated that: a) the residual phosphorus concentration was in the range of 1300 - 1500 mg/L for the preparation of type I feed grade calcium hydrogen phosphate from phosphogypsum leachate;b) the P removal effect could reach 99.99% for the preparation of calcium phosphate from phosphogypsum using the theoretical equation: fixation rate = 87.91 - 10.96(Ca/P) + 3.22(Ca/P)<sup>2</sup> (R<sup>2</sup> = 0.9954);c) The procedure follows the suggested secondary kinetics, and according to the Freundlich isothermal model, the reaction process is under the control of the chemical reaction, with a reaction index of 0.7605. This study can be used as a theoretical guide for the recovery of P from phosphogypsum leachate, the preparation of products to bring about economic by-products, and the purification of wastewater for reuse.展开更多
Ion migration is a notorious problem in perovskite solar cells(PSCs)that severely mutilates device performance.Herein,a strategy to inhibit ion migration in situ is developed by using photoisomerization of azobenzene(...Ion migration is a notorious problem in perovskite solar cells(PSCs)that severely mutilates device performance.Herein,a strategy to inhibit ion migration in situ is developed by using photoisomerization of azobenzene(AZO)to immobilize cations in the lattice.During the nucleation process,the photoisomerized cis-AZO reacts with FA^(+),MA^(+)and Pb2+cations in the perovskite precursor by synergistic cation-πinteraction and Lewis base coordination,leading to heterogeneous nucleation to produce uniform perovskite film.Meanwhile,it accelerates conversion of intermediate yellowδ-phase to desired black aphase of FAPb I3for improved crystallinity with well-passivated grain surface.Consequently,defect density is effectively reduced for the perovskite film to demonstrate suppressed carrier recombination and enhanced carrier extraction.Subsequently,the solar cell efficiency is elevated from 21.29%to 23.58%with negligible J-V hysteresis.Long-term stability is also improved,with the bare device without any encapsulation retaining 84%of its initial efficiency after aging 744 hours in ambient.展开更多
文摘After washing and curing, P is transported from the phosphogypsum to the leachate during the phosphogypsum detoxification process, providing two ideas for phosphorus recovery from phosphogypsum leachate: 1) preparation of calcium hydrogen phosphate for feed;2) preparation of calcium phosphate. A ready-to-use calcium oxide slurry was used to recover P from phosphogypsum leachate at a slurry concentration of 20% and a quantitative link between calcium to phosphorus ratio and fixation rate was fitted by mixed use batch experiments, reaction kinetics and thermodynamics, and theoretical calculations were used to demonstrate that phosphorus cannot be completely reused in the preparation of calcium hydrogen phosphate. The findings demonstrated that: a) the residual phosphorus concentration was in the range of 1300 - 1500 mg/L for the preparation of type I feed grade calcium hydrogen phosphate from phosphogypsum leachate;b) the P removal effect could reach 99.99% for the preparation of calcium phosphate from phosphogypsum using the theoretical equation: fixation rate = 87.91 - 10.96(Ca/P) + 3.22(Ca/P)<sup>2</sup> (R<sup>2</sup> = 0.9954);c) The procedure follows the suggested secondary kinetics, and according to the Freundlich isothermal model, the reaction process is under the control of the chemical reaction, with a reaction index of 0.7605. This study can be used as a theoretical guide for the recovery of P from phosphogypsum leachate, the preparation of products to bring about economic by-products, and the purification of wastewater for reuse.
基金supported by the National Natural Science Foundation of China(21603140)the 111 Project(B21005)。
文摘Ion migration is a notorious problem in perovskite solar cells(PSCs)that severely mutilates device performance.Herein,a strategy to inhibit ion migration in situ is developed by using photoisomerization of azobenzene(AZO)to immobilize cations in the lattice.During the nucleation process,the photoisomerized cis-AZO reacts with FA^(+),MA^(+)and Pb2+cations in the perovskite precursor by synergistic cation-πinteraction and Lewis base coordination,leading to heterogeneous nucleation to produce uniform perovskite film.Meanwhile,it accelerates conversion of intermediate yellowδ-phase to desired black aphase of FAPb I3for improved crystallinity with well-passivated grain surface.Consequently,defect density is effectively reduced for the perovskite film to demonstrate suppressed carrier recombination and enhanced carrier extraction.Subsequently,the solar cell efficiency is elevated from 21.29%to 23.58%with negligible J-V hysteresis.Long-term stability is also improved,with the bare device without any encapsulation retaining 84%of its initial efficiency after aging 744 hours in ambient.
