Leaching optimization and dissolution behavior of alkaline anions in bauxite residue

Bauxite residue is a highly alkaline waste containing soluble alkaline anions, which can cause environmental concerns. The optimal leaching conditions, distribution of alkaline anions, types of pivotal alkaline anions and their dissolution behaviors were investigated based on the combination of single factors-orthogonal experiments and leaching stage experiment. Using a two-stage leaching, 86% of the soluble alkaline anions（CO3^2-, HCO4^-,Al（OH）4^-, OH^-） were leached with a L/S ratio of 2 mL/g, at 30 ℃, over 23 h. During the first stage of leaching, approximately 88% of alkaline anions were leached from the dissolution of free alkali（Na OH, carbonate, bicarbonate, NaAl（OH）4） with the rest originating from the dissolution of alkaline minerals（calcite, cancrinite and hydrogarnet）. Supernatant alkalinity was 69.78 mmol/L with CO3^2- accounting for 75%. Furthermore, carbonate leaching was controlled by solid film diffusion using the Stumm Model with an apparent activation energy of 10.24 kJ/mol.

Dissolution behaviors of Ta_2O_5,Nb_2O_5 and their mixture in KOH and H_2O system

The dissolution behaviors of Ta2O5,Nb2O5 and their mixture in KOH and H2O system were investigated.A L9(34) orthogonal design was used to study the effects of reaction temperature,mass ratio of KOH to Ta2O5,and reaction time on the dissolution rate of tantalum.It was found that the effect of reaction temperature on the dissolution rate of tantalum was much greater than that of the other factors.The results of factorial experiments showed that Ta2O5 was mainly transformed into insoluble potassium tantalate at low temperature(350 ℃) and transformed into soluble potassium tantalate at high temperature(450 ℃).The insoluble potassium tantalate was analyzed by XRD,which was proved to be KTaO3.Differently,almost all Nb2O5 was transformed into soluble potassium niobate at 350-450℃.As for the mixture of Ta2O5 and Nb2O5,the dissolution rate of tantalum increased and the dissolution rate of niobium decreased as an interaction existed between niobium and tantalum.And increasing the mole ratio of Nb2O5 to Ta2O5 in the mixture was beneficial to the dissolution of both Ta2O5 and Nb2O5.In addition,the mechanism of the interaction between niobium and tantalum was also investigated through phase and chemical analysis.

Dissolution behaviors of rare earth elements in phosphoric acid solutions

In order to provide practical fundamental data for rare-earth elements （REEs） recovery from phosphoric acid and to betterunderstand REEs behavior during the phosphoric acid evaporation process, the solubilities of REEs in phosphoric acid with variousconcentrations of phosphorus at different temperatures were measured. A simple linear model between REEs solubility andphosphoric acid concentration is built and the experimental data are found to fit it very well （R2〉0.94）. Hydrogen-ion concentration isfound to be the predominant factor controlling the solubility of REEs in phosphoric acid. In addition, the solubility of REEs inphosphoric acid is found to sharply decrease with increasing temperature, which can be attributed to the increase of the Gibbs energyof the REEPO4 dissolution reaction or the restraint of the disassociation of phosphoric acid molecules owing to the elevatedtemperature.

Dissolution behavior of various elements from steelmaking slag into seawater

The mixture of steelmaking slag,soil or sand is a candidate material for the landfill in sea shore to improve the marine environment,because the ferrous ion contained in the steelmaking slag plays an important role in promoting the growth of various seaweeds.However,the dissolution mechanism of various elements from steelmaking slag into seawater is not clarified.To reveal the dissolution behavior of various elements from steelmaking slag into seawater,the dissolution experiment of slag and seawater mixture was conducted at room temperature with changing the basicity of slag and the mass ratio of slag and seawater.It is shown that Mg ion contained in the seawater plays a buffering action obviously on pH increase which is provided by the dissolution of Ca.The dissolution behavior of Si strongly depends on the basicity of slag,at the same time the mass ratio has a conspicuous influence on it for the lower basicity of slag.The dissolution amount of Fe is little and it is discussed by using the solubility diagram.

Comparison of electrochemical behaviors of Ti-5Al-2Sn-4Zr-4Mo-2Cr-1Fe and Ti-6Al-4V titanium alloys in NaNO_(3) solution

The Ti-5Al-2Sn-4Zr-4Mo-2Cr-1Fe(β-CEZ)alloy is considered as a potential structural material in the aviation industry due to its outstanding strength and corrosion resistance.Electrochemical machining(ECM)is an efficient and low-cost technology for manufacturing theβ-CEZ alloy.In ECM,the machining parameter selection and tool design are based on the electrochemical dissolution behavior of the materials.In this study,the electrochemical dissolution behaviors of theβ-CEZ and Ti-6Al-4V(TC4)alloys in NaNO3solution are discussed.The open circuit potential(OCP),Tafel polarization,potentiodynamic polarization,electrochemical impedance spectroscopy(EIS),and current efficiency curves of theβ-CEZ and TC4 alloys are analyzed.The results show that,compared to the TC4 alloy,the passivation film structure is denser and the charge transfer resistance in the dissolution process is greater for theβ-CEZ alloy.Moreover,the dissolved surface morphology of the two titanium-based alloys under different current densities are analyzed.Under low current densities,theβ-CEZ alloy surface comprises dissolution pits and dissolved products,while the TC4 alloy surface comprises a porous honeycomb structure.Under high current densities,the surface waviness of both the alloys improves and the TC4 alloy surface is flatter and smoother than theβ-CEZ alloy surface.Finally,the electrochemical dissolution models ofβ-CEZ and TC4 alloys are proposed.

Electrochemical dissolution and passivation of laser additive manufactured Ti6Al4V controlled by elements segregation and phases distribution

The electrochemical dissolution and passivation of laser additive manufactured Ti6Al4V were investigated through Tafel polarization,potentiostatic polarization and AC impedance measurements.The results show that the solution treatment−aging(STA)process aggravates the element micro-segregation compared to the annealing process,leading to varied Al and V contents of the phases from different samples.It is proven that either Al-rich or V-rich condition can highly affect the electrochemical dissolution behaviors due to thermodynamical instability caused by element segregation.The dissolution rate in the metastable passivation process is controlled by the stability of the produced film that is affected by phases distribution,especially the difficult-to-dissolve phase.And then,the dissolution rate of the phases in the transpassivation region is consistent with the rank in the activation process because the dense film is not capable of being produced.Compared to the annealed sample,the higher dissolution rate of the STA sample is beneficial to the electrochemical machining(ECM)of Ti6Al4V.

Dissolution kinetics of solid fuels used in COREX gasifier and its influence factors

Carbon dissolution from solid fuels used in a COREX gasifier was investigated in a high-temperature furnace to investigate the influences of temperature, carbon structure and ash properties of solid fuels into molten iron on carbon dissolution behavior. The results showed that the final carbon content of molten iron and dissolution reaction rate of carbon increased as the temperature increased. However, the dissolution behavior of different solid fuels varied with their properties. At the same temperature, the dissolution reaction rate of solid fuel from high to low was coke, semi-coke and lump coal. The apparent reaction rate constants of solid fuel were calculated using the piecewise fitting method based on the experimental data. The analyzed results showed that the dissolution rates of solid fuels had a good correlation with their microcrystalline structures. Moreover, the carbon crystallite structures of solid fuels used in COREX had greater influence on dissolution behavior than their ash properties.

The accumulation and toxicity of ZIF-8 nanoparticles in Corbicula fluminea

Metal-organic frameworks(MOFs)are promising new materials that have been intensively studied and possibly applied to various environmental remediation.However,little is known about the fate and risk of MOFs to living organisms in thewater environment.Here,the toxic effects of ZIF-8 nanoparticles(NPs)on benthic organisms were confirmed by sub-chronic toxicity experiments(7 and 14 days)using Corbicula fluminea as the model organism.With exposure doses ranging from 0 to 50 mg/L,ZIF-8 NPs induced oxidative stress behaviors similar to the hormesis effect in the tissues of C.fluminea.The oxidative stress induced by ZIF-8 NPs and the released Zn^(2+)was the crucial cause of the toxic effects.Besides,we also found that the ZIF-8 NPs and dissolved Zn^(2+)may result in different mechanisms of toxicity and accumulation depending on the dosages.The Zn^(2+)release rate of ZIF-8NPswas high at low dosages,leading to a higher proportion of Zn^(2+)taken up by C.fluminea than the particulate ZIF-8.Conversely,at high dosages,C.fluminea mainly ingested the ZIF-8 NPs and resulted in increased mortality.The results have important implications for understanding the fate and biological effects of ZIF-8 in natural aquatic environments.

Coatings of needle/stripe-like fluoridated hydroxyapatite on H2O2-treated carbon/carbon composites prepared by induction heating and hydrothermal methods

A hydroxyapatite （HA） coating was achieved on H2O2-treated carbon/ carbon （C/C） composite through hydrothermally treating and induction heating deposited CaHPO4 coating in an ammonia solution under ultrasonic water bath. Then, this HA coating was placed in a NH4F solution and hydrothermally treated again to fabricate fluorinated hydroxyapatite （FHA） coatings for 24 h at 353, 373, 393 and 413 K, respectively. The structure, morphology and chemical composition of the HA and FHA coatings were characterized by SEM, XRD, EDS and FTIR, and the adhesiveness and chemical stability of these FHA coatings were examined by a scratch test and an immersion test, respectively. The results showed that the as-prepared FHA coatings contained needle-like or stripe-like crystals, different from those of the HA coating. As the fluoridation temperature rose, the adhesiveness of the FHA coating first increased from 34.8 to 40.9 N at a temperature between 353 and 393 K, and then decreased to 24.2 N at 413 K, while the dissolution rate of the FHA coating decreased steadily. The reasons for the property variation of the FHA coatings were proposed by analyzing the morphology, composition and structure of the coatings.