Leaching process of germanium oxide dust

A thermodynamic analysis on the acid leaching process of germanium oxide dust and discussion on the behaviors of main substances of the dust in the leaching process were carried out. The effects of temperature, acid concentration, leaching time and stirring speed on the leaching rate of germanium were investigated. Based on the characteristic of the dust, the kinetics and reactive mechanism of acid leaching were studied. The results show that the leaching of the dust by acid belonged to ＂the unreacted core shrinking model＂ of producing solid outgrowth layer. The chemical reaction was controlled by inner diffusion process. The apparent activation energy of leaching process was 12.60 kJ/mol. The leaching reaction of germanium was determined to be mainly second order reaction. The optimum conditions were the reaction temperature of 363 K, the leaching time of 2.5 h, the stirring speed of 120 r/min, the solid-to-liquid ratio of 1/8 and the acid concentration of 120 g/L. Under these conditions, the leaching rate of germanium can come up to more than 87%.

Readsorption of rare earth elements during leaching process of ion-adsorption-type rare earth ore

A leaching experiment on simulated rare earth ore pillars with uneven grade distribution was conducted because of the readsorption of rare earth elements in the in situ leaching process of ion-adsorption-type rare earth ore.Results show that the readsorption of rare earth elements in the barren layer is the main reason for the decrease in rare earth concentration in the leachate,decrease in rare earth recovery and extension of the leaching process.This limitation could be affected by the concentration of rare earth of the influent flow passing through the barren ore layer,and pH value of leaching agents shows minimal effect during leaching.The magnesium sulfate leaching process requires higher liquid-tosolid ratio than the ammonium sulfate leaching process.The former also has lower peak value of rare earth concentration and more significant tailing in the leaching curve.The readsorption of rare earth elements in the barren layer is more severe in magnesium sulfate leaching than in ammonium sulfate leaching.Thus,areas without ore belts should be avoided when magnesium sulfate is used for leaching.

Process optimization of rare earth and aluminum leaching from weathered crust elution-deposited rare earth ore with compound ammonium salts

In order to intensify the leaching process of rare earth（RE） and reduce the impurities in the leachate, ammonium chloride（NH4Cl） and ammonium nitrate（NH4NO3） were mixed as a compound leaching agent to treat the weathered crust elution-deposited RE ore. Effects of molar ratio of NH~＋_4Cl and NH_4NO_3, ammonium（NH_4） concentration, leaching agent pH and flow rate on the leaching process of RE were studied and evaluated by the chromatographic plate theory. Leaching process of the main impurity aluminium（Al） was also discussed in detail. Results showed that a higher initial ammonium concentration in a certain range could enhance the mass transfer process of RE and Al by providing a driving force to overcome the resistance of diffusion. pH almost had no effects on the mass transfer efficiency of RE and Al in the range of 4 to 8. The relationship between the flow rate and height equivalent to a theoretical plate（HETP） could fit well with the Van Deemter equation, and the flow rate at the lowest HETP was determined. The optimum conditions of column leaching for RE and Al were 1：1（molar ratio） of NH_4Cl and NH_4NO_3, 0.2 mol/L of ammonium concentration, pH 4–8 of leaching agent and 0.5 mL /min of flow rate. Under this condition, the mass transfer efficiency of RE was improved, but no change was observed for Al compared with the most widely used ammonium sulfate. Moreover, the significant difference value（around 20 mL） of retention volume at the peak concentration between RE and Al provided a possibility for their separation. It suggested the potential application of the novel compound leaching agent（NH_4Cl/NH_4NO_3）. It was found that the relative concentration of RE in the leachate could be easily obtained by monitoring the pH of leachate.

Effects of aging process on adsorption–desorption and bioavailability of fomesafen in an agricultural soil amended with rice hull biochar

Biochar has been introduced as an acceptable soil amendment due to its environmental benefits such as sequestering soil contaminants. However, the aging process in biochar amended soil probably decreases the adsorption capacity of biochar through changing its physico-chemical properties. Adsorption, leaching and bioavailability of fomesafen to corn in a Chinese soil amended by rice hull biochar after 0, 30, 90 and 180 days were investigated. Results showed that the addition of 0.5%-2% fresh biochar significantly increases the adsorption of fomesafen 4-26 times compare to unamended soil due to higher SSA of biochar. Biochar amendment also decreases fomesafen concentration in soil pore water by 5%-23% resulting lower risk of the herbicide for cultivated plants. However, the aging process decreased the adsorption capacity ofbiochar since the adsorption coefficient values which was 1.9-12.4 in 0.5%-2% fresh biochar amended soil, declined to 1.36-4.16, 1.13-2.78 and 0.95-2.31 in 1, 3 and 6-month aged treatments, respectively. Consequently, higher desorption, leaching and bioavailable fraction of fomesafen belonged to 6-month aged treatment. Nevertheless, rice hull biochar was effective for sequestering fomesafen as the adsorption capacity of biochar amended soil after 6 months of aging was still 2.5-5 times hi^her compared to that of unamended soil.

Synthesis of ZrC Nanoparticles in the ZrO_2–Mg–C–Fe System Through Mechanically Activated Self-Propagating High-Temperature Synthesis

ZrC nanoparticles in the matrix of Fe were produced by the mechanically activated self-propagating hightemperature method using ZrO2/C/Mg/Fe powder mixtures. The effects of milling time, Fe content, and combustion temperature as well as the formation route for synthesizing ZrC powder particles were studied. The samples were characterized by XRD, SEM, TEM, and DTA. The XRD results revealed that, after 18 h of mechanical activation, ZrO2/ZC/Mg/Fe reacted with the self-propagating combustion（SHS） mode at 870 °C producing the ZrC–Fe nanocomposite. It was also found that both mechanical activation and Fe content played key roles in the ZrC synthesis temperature. With a Fe content of（5–40） wt%, the SHS reaction proceeded favorably and both the ZrC formation temperature and the adiabatic temperature（Tad） decreased. The Mg O content was removed from the final products using a leaching test process by dissolving in hydrochloric and acetic acids.