镁化焙烧钒渣中钒的酸浸动力学研究

为了促进钒渣镁化焙烧−酸浸提钒法的工业应用,研究钒渣镁化焙烧熟料中钒的酸浸出动力学。结合XRD、XPS和SEM,揭示在浸出初期的10 min内,MgSiO_(3)和大部分钒酸盐急剧地消耗酸,形成SiO2和V(V)的氧钒根离子。通过研究钒浸出效率随浸出时间的变化,建立钒浸出的动力学模型。结果表明,浸出过程分为两个不同的阶段,且两个阶段的动力学均遵循收缩核模型。0~10 min的浸出速率由固体产物层扩散和化学反应共同控制,而10~30 min的浸出速率仅由化学反应控制。因此,浸出初始10 min内加速传质很关键,而后续20 min内精确控温至关重要。

Dual-Defect Engineering Strategy Enables High-Durability Rechargeable Magnesium-Metal Batteries

Rechargeable magnesium-metal batteries(RMMBs)are promising next-generation secondary batteries;however,their development is inhibited by the low capacity and short cycle lifespan of cathodes.Although various strategies have been devised to enhance the Mg^(2+)migration kinetics and structural stability of cathodes,they fail to improve electronic conductivity,rendering the cathodes incompatible with magnesium-metal anodes.Herein,we propose a dual-defect engineering strategy,namely,the incorporation of Mg^(2+)pre-intercalation defect(P-Mgd)and oxygen defect(Od),to simultaneously improve the Mg^(2+)migration kinetics,structural stability,and electronic conductivity of the cathodes of RMMBs.Using lamellar V_(2)O_(5)·nH_(2)O as a demo cathode material,we prepare a cathode comprising Mg_(0.07)V_(2)O_(5)·1.4H_(2)O nanobelts composited with reduced graphene oxide(MVOH/rGO)with P-Mgd and Od.The Od enlarges interlayer spacing,accelerates Mg^(2+)migration kinetics,and prevents structural collapse,while the P-Mgd stabilizes the lamellar structure and increases electronic conductivity.Consequently,the MVOH/rGO cathode exhibits a high capacity of 197 mAh g^(−1),and the developed Mg foil//MVOH/rGO full cell demonstrates an incredible lifespan of 850 cycles at 0.1 A g^(−1),capable of powering a light-emitting diode.The proposed dual-defect engineering strategy provides new insights into developing high-durability,high-capacity cathodes,advancing the practical application of RMMBs,and other new secondary batteries.

选择性还原分离和回收酸性浸出液中的碲和铋

提出一种用Na_(2)SO_(3)和Fe粉选择性分离和回收碲铋矿酸性浸出液中碲、铋的简单、高效方法。采用SEM-EDS、XRD、XPS和ICP-OES等手段研究碲、铋的选择性还原机理。过剩系数为16的Na_(2)SO_(3)在80℃和10 min条件下可还原99.83%的Te,粗碲品位达93.78%。此外,搅拌促进Na_(2)SO_(3)溶解,从而加速Te还原。过剩系数为7.5的Fe在60℃和40 min条件下可置换99.39%的Bi,粗铋品位达92.35%。采用循环浸出碲铋矿的方法可提高浸出液中Te(Ⅳ)和Bi(Ⅲ)的浓度并降低Fe(Ⅲ)的浓度,减少Na_(2)SO_(3)的消耗。

Microemulsion leaching of vanadium from sodium-roasted vanadium slag by fusion of leaching and extraction processes

The fusion of the leaching and purification processes was realized by directly using microemulsion as the leaching agent.The bis-(2-ethyhexyl)phosphoric acid(DEHPA)/n-heptane/NaOH microemulsion system was established to directly leach vanadates from sodium-roasted vanadium slag.The effect of the leaching agent on the leaching efficiency was investigated,in addition to the molar ratio of H_(2)O/NaDEHP(W),DEHPA concentration,solid/liquid ratio,stirring time,and leaching temperature.In optimal situations,the vanadium leaching efficiency reaches 79.57%.The X-ray diffraction characterization of the leaching residue and the Raman spectrum of the microemulsion before and after leaching demonstrate the successful entry of vanadates from the sodium-roasted vanadium slag into the microemulsion.The proposed method successfully realizes the leaching and purification of vanadates in one step,thereby greatly reducing production costs and environmental pollution.It also offers a new way to achieve the green recovery of valuable metals from solid resources.

Mass transfer of phosphorus in high-phosphorus hot-metal refining

Mass transfer of phosphorus in high-phosphorus hot-metal refining was investigated using CaO-FetO-SiO2 slags at 1623 K. Based on a two-film theory kinetic model and experimental results, it was found that the overall mass transfer coefficient, which includes the effects of mass transfer in both the slag phase and metal phase, is in the range of 0.0047 to 0.0240 cm/s. With the addition of a small amount of fluxing agents A1203 or Na20 into the slag, the overall mass transfer coefficient has an obvious increase. Silicon content in the hot metal also influences the overall mass transfer coefficient. The overall mass transfer coefficient in the lower [Si] heat is much higher than that in the higher [Si] heat. It is concluded that both fluxing agents and lower [Si] hot metal facilitate mass transfer of phosphorus in liquid phases. Fur- thermore, the addition of Na20 could also prevent rephosphorization at the end of the experiment.

Quick valence analysis method of vanadium toward accurate toxicity assessment of vanadium-containing hazardous wastes

In order to develop a quick, efficient and sensitive valence analysis method of vanadium(Ⅴ), the highperformance liquid chromatography(HPLC) was utilized to separate and quantify EDTA-complexed Ⅴ(Ⅲ), Ⅴ(Ⅳ) and Ⅴ(Ⅴ) ions. The influence of EDTA, TBAOH, solution pH and organic modifier on retention behavior of V-EDTA complexes was investigated. Complexed Ⅴ(Ⅲ), Ⅴ(Ⅳ) and Ⅴ(Ⅴ) ions can be separated and quantified in 5 min, with detection limits of 0.04 mg/L Ⅴ(Ⅲ), 0.07 mg/L Ⅴ(Ⅳ), and 0.06 mg/L Ⅴ(Ⅴ), respecti vely. The established method is applied to analyzing the hazardous waste of V-Cr-bearing reducing slag and results demonstrate 49.94% of its Ⅴ element to be toxic Ⅴ(Ⅴ). This work opens a new avenue for quick and accurate toxicity assessment of hazardous wastes containing multivalent heavy metals.

Slag formation path during dephosphorization process in a converter

The slag formation path is important for efficient dephosphorization in steelmaking processes. The phosphorus capacity and the melting properties of the slag are critical parameters for optimizing the slag formation path. Regarding these two factors, the phosphorus partition ratio was calculated using the regular solution model （RSM）, whereas the liquidus diagrams of the slag systems were estimated using the FactSage thermodynamic package. A slag formation path that satisfies the different requirements of dephosphorization at different stages of dephosphorization in a converter was thus established through a combination of these two aspects. The composition of the initial slag was considered to be approximately 15wt%CaO-44wt% SiOz-41wt%FeO. During the dephosphorization process, a slag formation path that follows a high-iron route would facilitate efficient dephosphorization. The composition of the final dephosphorization slag should be approximately 53wt%CaO-25.Swt% SiO2-21.5wt%FeO. The composition of the final solid slag after dephosphorization is approximately 63.6wt%CaO-30.3wt%SiO2-6. 1wt%FeO.

Solidification and heat transfer of molten steel slag particles during air quenching process

In order to effectively utilize the resources and energy of molten steel slag,the variation of precipitation phase and specific heat of air quenched steel slag(AQSS)particles during continuous cooling process was investigated by FactSage and thermogravimetry differential scanning calorimetry.The cooling and solidification process of molten AQSS particles was simulated by Fluent.The microstructure changes in AQSS particles in solidification process were analyzed using an ultrahigh temperature laser confocal microscope and a scanning electron microscope.The results indicated that in the cooling process of molten AQSS particles,the precipitation of Ca_(2)Fe_(2)O_(5) resulted in the largest change of specific heat.Under the condition of slow cooling,the cooling rate is more obviously affected by specific heat.When the initial air velocity was 300 m s^(-1),there was the highest temperature difference in AQSS particles during cooling process.What is more,the compactness of the boundary region of AQSS particles was obviously better than that of its central region.

A critical review of vanadium-based electrode materials for rechargeable magnesium batteries

Rechargeable magnesium batteries(RMBs)are one of the most promising next-generation energy storage devices due to their high safety and low cost.With a large family and versatile advantageous structures,vanadium-based compounds are highly competitive as electrode materials of RMBs.This review summa-rizes the structural characteristics,electrochemical performance,and refinement methods of vanadium-based materials,including vanadium oxides,vanadium sulfides,vanadates,vanadium phosphates,and vanadium spinel compounds,as RMB cathodes.Although relatively less,vanadium-based materials as RMB anodes are also introduced.According to the application requirements of RMBs,present common strategies are concluded to improve the electrochemical performance of vanadium-based materials;the probably promising development directions are also proposed,which are not limited only to the elec-trode materials,but also the compatible electrolytes and separator materials.In the near future,RMBs are expected from their large-scale application,standing at the forefront of the energy storage era.