High-purity magnesium ammonium phosphate （MAP） was precipitated by controlling pH value of the reaction system of 9.0-9.5. The thermal decomposition behavior of MAP and the adsorption properties of its pyrolysis pro...High-purity magnesium ammonium phosphate （MAP） was precipitated by controlling pH value of the reaction system of 9.0-9.5. The thermal decomposition behavior of MAP and the adsorption properties of its pyrolysis products toward ammonia-nitrogen were also studied by XRD, SEM, TGA-DTA and FT-IR methods. The results indicated that high-purity MAP was obtained at pH value of 9.0-9.5. Upon heating to 100-120℃ for 120 min, MAP was thermally decomposed, losing water and ammonia concomitantly with a reduction in grain size and crystallinity. The capacity of pyrolysis products for ammonia nitrogen adsorption reached 72.5 mg/g, with a removal rate of up to 95% from an 800 mg/L solution. The characteristic diffraction peaks corresponding to MAP mainly appeared in their XRD patterns after adsorption of ammonia nitrogen. The pyrolysis products of MAP at 100-120 ℃ could be recycling-used as the chemical treatment regents of ammonia nitrogen in the practical application.展开更多
With on-line coupled thermo-gravimetric technique, the thermal decomposition of analyzer-Fourier transform infrared spectrometer lithium hexafluorophosphate （LiPF6） and its gas evolution at inert environment （H2O〈...With on-line coupled thermo-gravimetric technique, the thermal decomposition of analyzer-Fourier transform infrared spectrometer lithium hexafluorophosphate （LiPF6） and its gas evolution at inert environment （H2O〈10 ppm） were studied under both non-isothermal and isothermal conditions. The results showed that the LiPF6 decomposition is a single-stage reaction with LiF as final residue and PF5 as gas product. In addition, its decomposi- tion kinetics was determined as 2D phase boundary movement （cylindrical symmetry） under both non-isothermal and isothermal conditions. Furthermore, the activation energy of LiPF6 decomposition was calculated as 104 and 92 kJ/mol for non-isothermal and isothermal con- ditions, respectively.展开更多
Hierarchical nanostructures have attracted widespread interest owing to their unique properties compared to their bulk counterparts. Thus, they are considered promising electrocatalytic materials. In this work, a nove...Hierarchical nanostructures have attracted widespread interest owing to their unique properties compared to their bulk counterparts. Thus, they are considered promising electrocatalytic materials. In this work, a novel hierarchical porous nanocomposite of cobalt phosphide nanocage@ferric-zinc mixed-metal phosphide nanotubes(denoted Co P@Zn Fe P) was fabricated using a self-assembly approach. Because of their structural and compositional merits, the as-prepared phosphide hybrids have abundant catalytic active sites and high porosity for facile mass diffusion. In an alkaline electrolyte, the CoP@ZnFeP flower-like hybrids displayed enhanced catalytic activity for the hydrogen evolution reaction and the oxygen evolution reaction compared with a mechanical mixture of Co P and Zn Fe P nanoparticles. The CoP@ZnFeP hierarchical nanocomposites also showed excellent activity for the overall water splitting reaction, yielding a water-splitting current of 10 mA/cm^2 on the application of just 1.6 V, as well as excellent durability(24-h long-term operation) in a two-electrode system. Our design methodology may create opportunities to search for highly efficient and robust non-precious metal catalysts with applications in high-performance energy conversion and storage devices.展开更多
Leaching soluble phosphorus from rock phosphate containing pyrites by Acidithiobacillus ferrooxidans (A.f.) is feasible, and the reaction mechanism is as follows. Pyrites are oxidized by A.f. to produce H_2SO_4 and Fe...Leaching soluble phosphorus from rock phosphate containing pyrites by Acidithiobacillus ferrooxidans (A.f.) is feasible, and the reaction mechanism is as follows. Pyrites are oxidized by A.f. to produce H_2SO_4 and FeSO_4; the rock phosphate is decomposed by H_2SO_4, forming soluble phosphorus compounds; and Fe2+ from FeSO_4 is oxidized to Fe^3+, providing energy for the growth of A. f.. In this process, as H_2SO_4 is produced in the reaction, an acidic condition in the culture medium is formed, which benefits the growth of A. f. and aids both continuous oxidation of pyrites and leaching of soluble phosphorus from rock phosphate. The fraction of phosphorous leached can reach the largest in the presence of 1.0 g/L Fe^3+, 200 mg/L Mg^2+ and 400 mg/L NH_4^+. The optimal technological parameters on the fraction of phosphorous leached are as follows: the volume fraction of inocula of A. f., the mass ratio of pyrites to rock phosphate and the pH value are in ranges of 5%-25%, 3:1-5:1 and 1.8-2.2, respectively.展开更多
基金Project(ZDSY20120619093952884)supported by Shenzhen Strategic New Industry Development,China
文摘High-purity magnesium ammonium phosphate （MAP） was precipitated by controlling pH value of the reaction system of 9.0-9.5. The thermal decomposition behavior of MAP and the adsorption properties of its pyrolysis products toward ammonia-nitrogen were also studied by XRD, SEM, TGA-DTA and FT-IR methods. The results indicated that high-purity MAP was obtained at pH value of 9.0-9.5. Upon heating to 100-120℃ for 120 min, MAP was thermally decomposed, losing water and ammonia concomitantly with a reduction in grain size and crystallinity. The capacity of pyrolysis products for ammonia nitrogen adsorption reached 72.5 mg/g, with a removal rate of up to 95% from an 800 mg/L solution. The characteristic diffraction peaks corresponding to MAP mainly appeared in their XRD patterns after adsorption of ammonia nitrogen. The pyrolysis products of MAP at 100-120 ℃ could be recycling-used as the chemical treatment regents of ammonia nitrogen in the practical application.
文摘With on-line coupled thermo-gravimetric technique, the thermal decomposition of analyzer-Fourier transform infrared spectrometer lithium hexafluorophosphate （LiPF6） and its gas evolution at inert environment （H2O〈10 ppm） were studied under both non-isothermal and isothermal conditions. The results showed that the LiPF6 decomposition is a single-stage reaction with LiF as final residue and PF5 as gas product. In addition, its decomposi- tion kinetics was determined as 2D phase boundary movement （cylindrical symmetry） under both non-isothermal and isothermal conditions. Furthermore, the activation energy of LiPF6 decomposition was calculated as 104 and 92 kJ/mol for non-isothermal and isothermal con- ditions, respectively.
基金supported by the Natural Science Foundation of Shandong Province(ZR2018BB061,ZR2018BB060,ZR2018LB004)~~
文摘Hierarchical nanostructures have attracted widespread interest owing to their unique properties compared to their bulk counterparts. Thus, they are considered promising electrocatalytic materials. In this work, a novel hierarchical porous nanocomposite of cobalt phosphide nanocage@ferric-zinc mixed-metal phosphide nanotubes(denoted Co P@Zn Fe P) was fabricated using a self-assembly approach. Because of their structural and compositional merits, the as-prepared phosphide hybrids have abundant catalytic active sites and high porosity for facile mass diffusion. In an alkaline electrolyte, the CoP@ZnFeP flower-like hybrids displayed enhanced catalytic activity for the hydrogen evolution reaction and the oxygen evolution reaction compared with a mechanical mixture of Co P and Zn Fe P nanoparticles. The CoP@ZnFeP hierarchical nanocomposites also showed excellent activity for the overall water splitting reaction, yielding a water-splitting current of 10 mA/cm^2 on the application of just 1.6 V, as well as excellent durability(24-h long-term operation) in a two-electrode system. Our design methodology may create opportunities to search for highly efficient and robust non-precious metal catalysts with applications in high-performance energy conversion and storage devices.
基金Project(2004CB619200) supported by the State Basic Research Development Program of ChinaProject(Z200515002) supported by the Key Project Foundation of the Education Department of Hubei Province, China
文摘Leaching soluble phosphorus from rock phosphate containing pyrites by Acidithiobacillus ferrooxidans (A.f.) is feasible, and the reaction mechanism is as follows. Pyrites are oxidized by A.f. to produce H_2SO_4 and FeSO_4; the rock phosphate is decomposed by H_2SO_4, forming soluble phosphorus compounds; and Fe2+ from FeSO_4 is oxidized to Fe^3+, providing energy for the growth of A. f.. In this process, as H_2SO_4 is produced in the reaction, an acidic condition in the culture medium is formed, which benefits the growth of A. f. and aids both continuous oxidation of pyrites and leaching of soluble phosphorus from rock phosphate. The fraction of phosphorous leached can reach the largest in the presence of 1.0 g/L Fe^3+, 200 mg/L Mg^2+ and 400 mg/L NH_4^+. The optimal technological parameters on the fraction of phosphorous leached are as follows: the volume fraction of inocula of A. f., the mass ratio of pyrites to rock phosphate and the pH value are in ranges of 5%-25%, 3:1-5:1 and 1.8-2.2, respectively.
