Mössbauer investigation of Co-doped Bismuth Ferrite prepared by the solution method

In this work, [Formula: see text] ([Formula: see text] = 0, 0.08) nanoparticles were synthesized by the solution method and their structural differences were studied. X-ray diffraction results show that the rhombohedral R3c space group and perovskite structures are detected in both samples, accompanied by an impurity phase. The (104) and (110) peaks merge when cobalt ions are doped. The decrease in lattice parameters indicates that the microstructure of the nanoparticles becomes gradually distorted. Mössbauer spectroscopy analysis at room temperature reveals an additional doublet due to the oxygen vacancies in [Formula: see text]. Hyperfine interactions, spatial spin-modulated structures and oxygen deficiencies around iron ions are also reflected in the observed spectra and variations in hyperfine parameters.

Utilization of Metallurgy—Beneficiation Combination Strategy to Decrease TiO2 in Titanomagnetite Concentrate before Smelting

Excessive TiO2 in titanomagnetite concentrates (TC) causes unavoidable problems in subsequent smelting. At present, this issue cannot be addressed using traditional mineral processing technology. Herein, a strategy of metallurgy-beneficiation combination to decrease the TiO2 grade in TC before smelting was proposed. Roasting TC with calcium carbonate (CaCO3) together with magnetic separation proved to be a viable strategy. Under optimal conditions (roasting temperature = 1400 °C, CaCO3 ratio = 20%, and magnetic intensity = 0.18 T), iron and titanium was separated efficiently (Fe grade: 56.6 wt.%; Fe recovery: 70 wt.%; TiO2 grade 3 wt.%; TiO2 removal: 84.1 wt.%). X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy analysis were used to study the mechanisms. The results showed that Ti in TC could react with CaO to form CaTiO3, and thermodynamic calculations provided a relevant theoretical basis. In sum, the metallurgy-beneficiation combination strategy was proven as an effective method to decrease unwanted TiO2 in TC.

A Comparative Analysis of Vanadyl Porphyrins Isolated from Resins of Heavy Oils with High and Low Vanadium Content

The composition of purified vanadyl porphyrins recovered from the resins of heavy oils possessing high and low vanadium contents was investigated. Vanadium content in the resins of the heavy oils under study differs by a factor of ca. 15. To recover and purify vanadyl porphyrins from the resins, extraction by N,N–dimethylformamide (DMF) with subsequent two-stage column chromatography on silica gel and sulfocationite were employed. The change of structural-group composition and content of vanadyl porphyrins in the products obtained at each stage was evaluated using Fourier IR and UV-Vis spectroscopy. Analysis of the purified vanadyl porphyrins using MALDI mass spectrometry determined distribution of their most abundant types (etio- and DPEP) and identified C27–C39 homologs for the resins possessing high vanadium content and C28–C39 homologs for the resins with low vanadium content.

Crystal structure change in multilayer GeH flakes by hydrogen desorption under ultrahigh vacuum environments

To confirm the feasibility of the theoretically proposed method of forming free-standing germanene [Araidai et al., J. Appl. Phys. 128, 125301 (2020).], we have experimentally investigated hydrogen desorption properties from the hydrogen-terminated germanane (GeH) flakes. Thermal desorption spectroscopy analysis revealed that hydrogen desorption occurred during the heating under an ultrahigh vacuum environment, corresponding to mass loss of 1.0 wt%. Moreover, we have found that using an ultrahigh vacuum ambient and short-time annealing for hydrogen desorption is a key to sustain the crystal structures.

Effect of Sodium Metabisulfite on Selective Flotation of Chalcopyrite and Molybdenite

Sodium metabisulfite (MBS) was used in this study for selective flotation of chalcopyrite and molybdenite. Microflotation tests of single and mixed minerals were performed to assess the floatability of chalcopyrite and molybdenite. The results of microflotation of single minerals showed that MBS treatment significantly depressed the floatability of chalcopyrite and slightly reduced the floatability of molybdenite. The results of microflotation of mixed minerals demonstrated that the MBS treatment could be used as a selective chalcopyrite depressant in the selective flotation of chalcopyrite and molybdenite. Furthermore, the addition of diesel oil or kerosene could significantly improve the separation efficiency of selective flotation of chalcopyrite and molybdenite using MBS treatment. A mechanism based on X-ray photoelectron spectroscopy analysis results is proposed in this study to explain the selective depressing effect of MBS on the flotation of chalcopyrite and molybdenite.

The Importance of Molybdenum(IV) Active Sites in Promoting Electrochemical Reduction of N2 to NH3 with MoFe Bimetallic Catalysts

To overcome the low faradaic efficiency (FE) of single Mo or Fe based electrocatalysts in nitrogen reduction reactions (NRR) due to the competition from the hydrogen evolution reaction (HER), a series of bimetallic MoFe compound catalysts were prepared under an NH3 atmosphere through a facile precipitation-pyrolysis method. The formed tetravalent Mo was found to be capable of inducing better electronic interactions between the surface nitrogen species and the Fe metal groups, thus improving the FE. It was demonstrated that the prepared ternary MoFe-N catalyst exhibited a remarkable FE of 33.26 % and a high NH3 yield of 33.31 μg h-1 mg-1cat. for NRR, which was believed to have been caused by an obvious change in the valence of Mo that resulted in a lower HER activity. X-ray photoelectron spectroscopy analysis further revealed that thermal processing under an NH3 atmosphere formed the Mo(IV) active sites in Mo-N bond, which led to a significant suppression in HER activity. Finally, through the study of the surface hydrogenation mechanism, it was concluded that the synergistic effect of the adsorbed H* and Mo active sites was the main reason for the improved performance of NRR.