An efficient process based on oxidizing roasting−direct reduction−smelting−electrorefining was developed to separate and recover Zn,In,Ga and Fe from a typical hazardous jarosite residue.Phase transformation and eleme...An efficient process based on oxidizing roasting−direct reduction−smelting−electrorefining was developed to separate and recover Zn,In,Ga and Fe from a typical hazardous jarosite residue.Phase transformation and element migration during each separating process were evaluated by X-ray diffraction analysis(XRD),thermo-gravimetric−differential scanning calorimetry(TG−DSC),and scanning electron microscopy−energy dispersive spectrometry(SEM−EDS).The results show that the jarosite residue decomposed into hematite and zinc ferrite when oxidizing roasted at 1250℃ for 20 min.Then,Zn and In were volatilized and enriched into flue dust through the reductive roasting of oxidized pellets at 1200℃ for 60 min.Finally,Fe and Ga were separated by smelting−electrorefining of the reduced pellets to obtain high purity iron powder with 99.5%Fe and anode slime with 456 g/t Ga.Through the process,a total recovery of 97.42%Zn,87.86%In,90.70%Fe and 84.78%Ga can be achieved.展开更多
Calcium carboaluminate was successfully prepared by a simple and efficient one-step method,and the effects of temperature,time,raw material ratio,carbonate type and heavy CaCO_(3)particle size on the products were inv...Calcium carboaluminate was successfully prepared by a simple and efficient one-step method,and the effects of temperature,time,raw material ratio,carbonate type and heavy CaCO_(3)particle size on the products were investigated in detail.The results show that increasing the temperature and extending the reaction time can enhance the yield and crystallisation degree of calcium carboaluminate.The proportion of Ca(OH)_(2),Al(OH)_(3)and CaCO_(3)is a pivotal factor in the synthesis of calcium carboaluminate.When the ratio of Ca(OH)_(2),Al(OH)_(3)and CaCO_(3)is 3:2:1,the diffraction peaks of calcium carboaluminate in the products are relatively sharp and strong.Furthermore,the purity and crystallinity of the synthesized calcium carboaluminate are higher when heavy CaCO_(3)with the particle size of 120 mesh is used as the carbonate raw material,in comparison to CO_(2),Na_(2)CO_(3)and light CaCO_(3).As results,a simple and efficient method for the synthesis of calcium carboaluminate is proposed,which will provide a solid experimental foundation and technical support for the industrial application of calcium carboaluminate in marine concrete.展开更多
The three-dimensional(3D) Pd-based nanoflower structures,assembled from two-dimensional(2D)nanosheets,are characterized by their stable and ordered configurations.These structures have been extensively designed as ano...The three-dimensional(3D) Pd-based nanoflower structures,assembled from two-dimensional(2D)nanosheets,are characterized by their stable and ordered configurations.These structures have been extensively designed as anode materials for fuel cells.However,the exploration of trimetallic nanoflowers with porous architectures remains limited.In this study,we present a straightforward one-step solvothermal method for the synthesis of trimetallic Pd Cu Ni porous nanoflowers(PNFs).Leveraging several unique advantages,such as an open superstructure,high porosity,and enhanced electronic interactions among the trimetals,the resulting Pd Cu Ni PNFs demonstrate significantly improved electrochemical performance,with mass activities reaching 5.94 and 10.14 A/mg for the ethanol oxidation reaction(EOR)and the ethylene glycol oxidation reaction(EGOR),respectively.Furthermore,the Pd Cu Ni PNFs exhibit optimized d-band centers and the most negative onset oxidation potential,indicating enhanced antitoxicity and stability.This study not only provides a novel perspective on the synthesis of 3D porous nanomaterials but also highlights the potential application value of trimetallic nanoalloys in catalysis.展开更多
Electrochemical studies on silicon deposition were performed in molten salt electrolytes. Purification of metallurgical grade silicon by electrorefining was carried out in molten Si-chloride salts at temperatures from...Electrochemical studies on silicon deposition were performed in molten salt electrolytes. Purification of metallurgical grade silicon by electrorefining was carried out in molten Si-chloride salts at temperatures from 973 K to 1223 K. It was found that the use of a liquid alloy anode of silicon and copper was beneficial in molten CaCl2 with NaCl, CaO and dissolved Si. ICP-AES analysis results showed efficient removal of metal impurities, such as titanium, aluminum and iron, which are present in significant quantities in the feedstock. The contents of boron and phosphorus in the silicon after electrorefining were reduced from 36×10-6 and 25×10-6 to 4.6×10-6 and 2.8 ×10-6, respectively. The energy consumption of electrorefining was estimated to be about 9.3 kW?h/kg.展开更多
The electrochemical synthesis silicon wires by electrorefining metallurgical grade silicon in thermally dried and pre-electrolyzed molten KF-NaF eutectic were studied at temperatures 800-900 ℃ using cyclic voltammetr...The electrochemical synthesis silicon wires by electrorefining metallurgical grade silicon in thermally dried and pre-electrolyzed molten KF-NaF eutectic were studied at temperatures 800-900 ℃ using cyclic voltammetry and ac impedance. One oxidation peak at -0.14 V could be attributed to the reaction of Si to Si4＋. A cathodic peak occurred at -0.56 V in the cyclic voltammogram and one response semicircle in the ac impedance spectrum was observed, supporting a one-step electrochemical reduction process of Si4＋-→Si. The electrochemical reaction of silicon was controlled by the diffusion process. The purity of electrorefined silicon wires was up to 99.999% by ICP-MS analysis.展开更多
The present paper reports a new fluoride-free and energy-saving lead electrolytic refining process in order to solve the serious problems of the existing Betts lead electrorefining process, such as low production effi...The present paper reports a new fluoride-free and energy-saving lead electrolytic refining process in order to solve the serious problems of the existing Betts lead electrorefining process, such as low production efficiency,high energy consumption and fluorine pollution. In the process, a mixed solution of perchloric acid and lead perchlorate(HClO4-Pb(ClO4)2) with the additives of gelatin and sodium lignin sulfonate is employed as the new electrolyte. The cathodic polarization curves show that HClO4 is very stable, and there is no any reduction reaction of HClO4 during the electrolytic process. The redox reactions of lead ions in HClO4 solution are very reversible with an ultrahigh capacity efficiency, so the HClO4 acts as a stable support electrolyte with higher ionic conductivity than the traditional H2SiF6 electrolyte. The results of the scale-up experiments show that under the optimal conditions of 2.8 mol·L-1 HClO4, 0.4 mol·L-1 Pb(ClO4)2 and electrolysis temperature of 45 ℃, the energy consumption is as low as 24.5 kW·h·(t Pb)-1 , only about 20% of that by Betts method at the same current density of 20 mA·cm-2, and the purity of the refined lead is up to 99.9992%, much higher than that specified by Chinese national standard(99.994%, GB/T 469-2013) and European standard(99.99%, EN 12659–1999).展开更多
A new hydrometallurgical route for separation and recovery of Cu from Cu-As-bearing copper electrorefining black slime was developed. The proposed process comprised oxidation acid leaching of Cu-As-bearing slime and s...A new hydrometallurgical route for separation and recovery of Cu from Cu-As-bearing copper electrorefining black slime was developed. The proposed process comprised oxidation acid leaching of Cu-As-bearing slime and selective sulfide precipitation of Cu from the leachate. The effects of various process parameters on the leaching and precipitation of Cu and As were investigated. At the first stage, Cu extraction of 95.2% and As extraction of 97.6% were obtained at 80 ℃ after 4 h with initial H2 SO4 concentration of 1.0 mol/L and liquid-to-solid ratio of 10 mL/g. In addition, the leaching kinetics of Cu and As was successfully reproduced by the Avrami model, and the apparent activation energies were found to be 33.6 and 35.1 kJ/mol for the Cu and As leaching reaction, respectively, suggesting a combination of chemical reaction and diffusion control. During the selective sulfide precipitation, about 99.4% Cu was recovered as CuS, while only 0.1% As was precipitated under the optimal conditions using sulfide-to-copper ratio of 2.4:1, time of 1.5 h and temperature of 25 ℃.展开更多
Electrorefining of nickel in LiCl–KCl melt was investigated using electrochemical techniques. Nickel products after electrorefining were characterized by X-ray diffraction, X-ray fluorescence, and scanning electron m...Electrorefining of nickel in LiCl–KCl melt was investigated using electrochemical techniques. Nickel products after electrorefining were characterized by X-ray diffraction, X-ray fluorescence, and scanning electron microscopy. Both cyclic voltammetry and square wave voltammetry results suggested that Ni^2+ was directly reduced to Ni metal in LiCl–KCl. Based on a preliminary study on the electrochemical behavior of nickel and chromium, electrorefining was carried out under constant potential, whereupon deposits were formed on the cathode. The purity of nickel increased from 72.62% in the original alloy to 99.83% in cathodic deposits, as determined by inductively coupled plasma atomic emission spectroscopy analysis. Almost all the nickel in the alloy could be recovered during the electrochemical process with[90% current efficiency. A lower concentration of NiCl2 in LiCl– KCl was found to be favorable for nickel electrorefining, as increased NiCl2 concentration caused severe corrosion of the nickel anode at the gas–liquid interface due to the accumulation of Cl2 gas.展开更多
A practical approach was introduced to study the inclusion mechanism of chlorine in high purity copper electrorefining from nitric acid system via cyclic voltammetry(CV) combined with electrodeposition experiments. Th...A practical approach was introduced to study the inclusion mechanism of chlorine in high purity copper electrorefining from nitric acid system via cyclic voltammetry(CV) combined with electrodeposition experiments. The CV curves display an obvious reduction peak of Cu Cl intermediate, which can provide an insight into the electrochemical behavior of this inclusion. Experimental results show that the increase of HNO3 concentration is favorable to reducing the quantity of chlorine inclusion although there is a slight decline in cathodic current efficiency. The optimum conditions for copper electrorefining in nitric acid system are HNO3 concentration in solution of 1-2 mol/L, moderate temperature of ~35 ℃ with current density not exceeding 25 m A/cm2. Based on the theoretical studies, an optimized copper electrorefining experiment was designed to simulate the industrial electrolysis, by which high purity copper can be obtained with chlorine inclusion less than 10 μg/g and current efficiency higher than 90%.展开更多
The application of indium requires high purity indium as material, and the high purity indium has been prepared by electrorefining. The selection and preparation of electrolyte in electrorefining indium were investiga...The application of indium requires high purity indium as material, and the high purity indium has been prepared by electrorefining. The selection and preparation of electrolyte in electrorefining indium were investigated, and the effect of component of electrolytic solution on electrolytic refining was also studied. Compared with electrolyte of InCl3-HCl, electrolyte of In2（SO4）3-H2SO4 has higher stability and lower corrosivity, electrolytic solution can be heated at low temperature, and bath is open and simple, which makes operation more convenient. The results show that the voltage can be kept at 0.30.5 V, and the content of indium can exceed 99.999% when the content of indium（Ⅲ） ion and sodium chloride are 80120 g/L. The bench-scale test of electrolysis was carried out, and the product of indium reaches the national standard of 99.999% high purity indium.展开更多
The electrochemical behavior of Al(Ⅲ)in urea-1-butyl-3-methylimidazolium chloride-aluminum chloride(urea-BMIC-AlCl_(3))ionic liquids,and the effect of potential and temperature on the characterization of cathode prod...The electrochemical behavior of Al(Ⅲ)in urea-1-butyl-3-methylimidazolium chloride-aluminum chloride(urea-BMIC-AlCl_(3))ionic liquids,and the effect of potential and temperature on the characterization of cathode products,current efficiency and energy consumption of aluminum electrorefining have been investigated.Cyclic voltammetry showed that the electrochemical reduction of Al(Ⅲ)was a one-step three-electron-transfer irreversible reaction,and the electrochemical reaction was controlled by diffusion.The diffusion coefficient of Al(Ⅲ)in urea-BMIC-AlCl_(3)ionic liquids at 313 K was 1.94×10^(−7)cm^(2)/s.The 7075 aluminum alloy was used as an anode for electrorefining,and the cathode products were analyzed by XRD,SEM and EDS.The results from XRD analysis indicated that the main phase of the cathode products was aluminum.The results from SEM and EDS characterization revealed that the cathode product obtained by electrorefining−1.2 V(vs.Al)was dense and uniform,and the mass fraction of aluminum decreased from 99.61%to 99.10%as the experimental temperature increased from 313 K to 333 K.In this work,the optimum experimental conditions were−1.2 V(vs.Al)and 313 K.At this time,the cathode current efficiency was 97.80%,while the energy consumption was 3.72 kW·h/kg.展开更多
The influences of cupric ion concentration （5-35 g/L）,current density （500-2000 A/m2）,circulation rate of the electrolyte solution （15-120 mL/min）,and temperature （25-60℃） on the physical and chemical propert...The influences of cupric ion concentration （5-35 g/L）,current density （500-2000 A/m2）,circulation rate of the electrolyte solution （15-120 mL/min）,and temperature （25-60℃） on the physical and chemical properties of copper powders obtained in electrolysis cells were investigated.Two industrial processes,electrorefining （ER） cells with a synthetic electrolyte and electrowinning （EW） cells with an original solution of coppermineral leaching,were utilized to produce copper powders.Finally,the statistical full factorial method of design of experiments （DOE） was employed to investigate the interaction or the main effects of processes.The results show that increasing the copper concentration and temperature can increase the grain size,apparent density,and electrical energy consumption.On the other hand,increasing the current density and circulation rate of the electrolyte can decrease them.This production process is optimized via DOE to control the interactive and main effects to produce copper powders with favorable properties.展开更多
Oxygen release and electrolyte decomposition under high voltage endlessly exacerbate interfacial ramifications and structu ral degradation of high energy-density Li-rich layered oxide(LLO),leading to voltage and capac...Oxygen release and electrolyte decomposition under high voltage endlessly exacerbate interfacial ramifications and structu ral degradation of high energy-density Li-rich layered oxide(LLO),leading to voltage and capacity fading.Herein,the dual-strategy of Cr,B complex coating and local gradient doping is simultaneously achieved on LLO surface by a one-step wet chemical reaction at room temperature.Density functional theory(DFT)calculations prove that stable B-O and Cr-O bonds through the local gradient doping can significantly reduce the high-energy O 2p states of interfacial lattice O,which is also effective for the near-surface lattice O,thus greatly stabilizing the LLO surface,Besides,differential electrochemical mass spectrometry(DEMS)indicates that the Cr_(x)B complex coating can adequately inhibit oxygen release and prevents the migration or dissolution of transition metal ions,including allowing speedy Li^(+)migration,The voltage and capacity fading of the modified cathode(LLO-C_(r)B)are adequately suppressed,which are benefited from the uniformly dense cathode electrolyte interface(CEI)composed of balanced organic/inorganic composition.Therefore,the specific capacity of LLO-CrB after 200 cycles at 1C is 209.3 mA h g^(-1)(with a retention rate of 95.1%).This dual-strategy through a one-step wet chemical reaction is expected to be applied in the design and development of other anionic redox cathode materials.展开更多
In this work,one-step growth models using hyperspectral imaging(HSI)(400-1000 nm)were successfully developed in order to estimate the microbial loads,minimum growth temperature(T_(min))and maximum specific growth rate...In this work,one-step growth models using hyperspectral imaging(HSI)(400-1000 nm)were successfully developed in order to estimate the microbial loads,minimum growth temperature(T_(min))and maximum specific growth rate(μ_(max))of Brochothrix thermosphacta in chilled beef at isothermal temperatures(4-25℃).Three different methods were compared for model development,particularly using(Model Ⅰ)the predicted microbial loads from partial least squares regression of the whole spectral variables;(Model Ⅱ)the selected spectral variables related to microbial loads;and(Model Ⅲ)the first principal scores of HSI spectra by principal component analysis.Consequently,Model Ⅰ showed the best ability to predict the microbial loads of B.thermosphacta,with the coefficient of determination(R_(v)^(2))and root mean square error in internal validation(RMSEV)of 0.921 and 0.498(lg(CFU/g)).The T_(min)(-12.32℃)andμmax can be well estimated with R^(2) and root mean square error(RMSE)of 0.971 and 0.276(lg(CFU/g)),respectively.The upward trend ofμmax with temperature was similar to that of the plate count method.HSI technique thus can be used as a simple method for one-step growth simulation of B.thermosphacta in chilled beef during storage.展开更多
BACKGROUND Inflammatory bowel disease(IBD)is a common chronic intestinal inflammatory disease.High oxidative stress is a treatment target for IBD.Cerium oxide(CeO2)nanomaterials as nanozymes with antioxidant activity ...BACKGROUND Inflammatory bowel disease(IBD)is a common chronic intestinal inflammatory disease.High oxidative stress is a treatment target for IBD.Cerium oxide(CeO2)nanomaterials as nanozymes with antioxidant activity are potential drugs for the treatment of colitis.AIM To synthesize hollow cerium(H-CeO2)nanoparticles by one-step method and to validate the therapeutic efficacy of H-CeO2 in IBD.METHODS H-CeO2 was synthesized by one-step method and examined its characterization and nanoenzymatic activity.Subsequently,we constructed dextran sulfate so-dium(DSS)-induced colitis in mice to observe the effects of H-CeO2 on colonic inflammation.The effects of H-CeO2 on colon inflammation and reactive oxygen species(ROS)levels in IBD mice were detected by hematoxylin and eosin staining and dichlorofluorescein diacetate staining,respectively.Finally,the biological sa-fety of H-CeO2 on mice was evaluated by hematoxylin and eosin staining,blood routine,and blood biochemistry.RESULTS H-CeO2 nanoparticles prepared by the one-step method were uniform,monodi-sperse and hollow.H-CeO2 had a good ability to scavenge ROS,∙OH and∙OOH.H-CeO2 reduced DSS-induced decreases in body weight and colon length,colonic epithelial damage,inflammatory infiltration,and ROS accumulation.H-CeO2 administration reduced the disease activity index of DSS-induced animals from about 8 to 5.H-CeO2 had no significant effect on body weight,total platelet count,hemoglobin,white blood cell,and red blood cell counts in healthy mice.No significant damage to major organs was observed in healthy mice following H-CeO2 administration.CONCLUSION The one-step synthesis of H-CeO2 nanomaterials had good antioxidant activity,biosafety,and inhibited deve-lopment of DSS-induced IBD in mice by scavenging ROS.展开更多
Building a superhydrophobic coating on a carbon steel substrate is an effective strategy for enhancing metal protection.A practical approach to producing a series of superhydrophobic Ni/SiO_(2)composite coatings(SSN)u...Building a superhydrophobic coating on a carbon steel substrate is an effective strategy for enhancing metal protection.A practical approach to producing a series of superhydrophobic Ni/SiO_(2)composite coatings(SSN)using one-step electrodeposition method is shown.The effect of processing parameters on surface structure and wettability was thoroughly explored,resulting in the identification of three typical surface morphologies.The prepared coating with petal-like structure(SSN-3)obtained under the optimum parameters exhibited the best water repellency,achieving a contact angle of 162.7°and a sliding angle of 4.1°.The droplet bouncing behavior on SSN coatings surface was studied,and the delayed icing time was recorded.Meanwhile,the mechanical stability and chemical corrosion resistance of SSN coatings were focused.The superhydrophobic SSN-3 coating with unique surface structure exhibited excellent reliability.The anticorrosion mechanism of SSN-3 coating was discussed,and its corrosion protection efficiency was up to 98.5%.The superior properties of the superhydrophobic SSN-3 coating make it suitable for diverse applications.展开更多
A solid,fast-dissolving sodium silicate was used as an alkaline activator.Granulated blast furnace slag(GGBS),metakaolin(MK),and steel slag(SS)were used as the cementious components to prepare a ternary composite ceme...A solid,fast-dissolving sodium silicate was used as an alkaline activator.Granulated blast furnace slag(GGBS),metakaolin(MK),and steel slag(SS)were used as the cementious components to prepare a ternary composite cementitious material known as alkali-activated steel slag composite cementitious material(ASCM)by the"one-step method".The impacts of cementitious components,alkali activator modulus,and Na_(2)O%on the mechanical strength were investigated,and the hydration products and hydration kinetics of ASCM were analyzed.The experimental results reveal that XRD,FTIR,SEM,EDS,and exothermic heat of hydration show that when GGBS:MK:SS=60wt%:10wt%:30wt%,the activator modulus is 1.2,and the alkali content is 5.5wt%,the 28 d flexural strength of ASCM mortar is 12.6 MPa,and the compressive strength is 53.3 MPa,the hydration products consist of C-S-H gel/C-A-S-H gel,mullite(3Al_(2)O_(3)-2SiO_(2)),calcite(CaCO_(3)),quartz,etc.ASCM has a large initial hydration exotherm rate but a small cumulative exotherm.展开更多
The hydrogen evolution reaction(HER) is a key process in electrocatalytic water splitting for hydrogen production,yet it is often limited by sluggish H^(*)-OH adsorption and H*binding kinetics.We obtained Rumodified N...The hydrogen evolution reaction(HER) is a key process in electrocatalytic water splitting for hydrogen production,yet it is often limited by sluggish H^(*)-OH adsorption and H*binding kinetics.We obtained Rumodified Ni O nanoparticles(Ru-Ni O/NF) with enhanced HER properties by substituting ruthenium(Ru)for Ni atoms in the Ni O(200) crystalline facets on nickel foam by a one-step electrodeposition technique.This novel catalyst exhibits a significantly reduced H^(*)-OH adsorption energy and improved kinetics,with an overpotential of only 60 mV at 10 mA/cm^(2) and a Tafel slope of 26.19 mV/dec.The Ru-Ni O/NF maintains its activity for over 115 h,outperforming NiO/NF by reducing the overpotential by 177 mV.DFT calculations confirm that the addition of Ru to NiO enhances the HER kinetics by modifying the electronic structure,optimizing the surface chemistry,stabilizing the intermediates,lowering the energy barriers,and facilitating efficient charge transfer through a robust three-dimensional structure,resulting in a change in the rate-limiting step and a significant reduction in the Gibbs free energy.This study presents a highly efficient HER catalyst and offers insights into designing advanced NiO-based electrocatalysts by reducing reaction energy barriers.展开更多
The optimal condition for a one-step process removing organic compounds from coking wastewater by simultaneously synthesized organobentonite as a pretreatment was investigated.Results showed that sorption of organic c...The optimal condition for a one-step process removing organic compounds from coking wastewater by simultaneously synthesized organobentonite as a pretreatment was investigated.Results showed that sorption of organic compounds by organobentonite was positively correlated to the cation surfactant exchange on the bentonite and the octanol-water partition coefficient（Kow） of the solutes.With 0.75 g/L bentonite and 180 mg/L（60% of bentonite cation exchange capacity） cetyltrimethylammonium bromide,the removal efficiencies of the 16 polycyclic aromatic hydrocarbon（PAHs） specified by the US Environmental Protection Agency in coking wastewater except naphthalene were more than 90%,and that of benzo（a）pyrene was 99.5%.At the same time,the removal efficiencies of CODCr,NH3-N,volatile phenols,colour and turbidity were 28.6%,13.2%,8.9%,55% and 84.3%,respectively,and the ratio of BOD5/CODCr increased from 0.31 to 0.41.These results indicated that the one-step process had high removal efficiency for toxic and refractory hydrophobic organic compounds,and could improve the biodegradability of the coking wastewater.Therefore it could be a promising technology for the pretreatment of toxic and refractory organic wastewater.展开更多
基金Hunan Provincial Key Research and Development Project, China (No. 2022SK2075)National Natural Science Foundation of China (No. 52004339)。
文摘An efficient process based on oxidizing roasting−direct reduction−smelting−electrorefining was developed to separate and recover Zn,In,Ga and Fe from a typical hazardous jarosite residue.Phase transformation and element migration during each separating process were evaluated by X-ray diffraction analysis(XRD),thermo-gravimetric−differential scanning calorimetry(TG−DSC),and scanning electron microscopy−energy dispersive spectrometry(SEM−EDS).The results show that the jarosite residue decomposed into hematite and zinc ferrite when oxidizing roasted at 1250℃ for 20 min.Then,Zn and In were volatilized and enriched into flue dust through the reductive roasting of oxidized pellets at 1200℃ for 60 min.Finally,Fe and Ga were separated by smelting−electrorefining of the reduced pellets to obtain high purity iron powder with 99.5%Fe and anode slime with 456 g/t Ga.Through the process,a total recovery of 97.42%Zn,87.86%In,90.70%Fe and 84.78%Ga can be achieved.
基金Funded by the National Nature Science Foundation of China(No.52078321)。
文摘Calcium carboaluminate was successfully prepared by a simple and efficient one-step method,and the effects of temperature,time,raw material ratio,carbonate type and heavy CaCO_(3)particle size on the products were investigated in detail.The results show that increasing the temperature and extending the reaction time can enhance the yield and crystallisation degree of calcium carboaluminate.The proportion of Ca(OH)_(2),Al(OH)_(3)and CaCO_(3)is a pivotal factor in the synthesis of calcium carboaluminate.When the ratio of Ca(OH)_(2),Al(OH)_(3)and CaCO_(3)is 3:2:1,the diffraction peaks of calcium carboaluminate in the products are relatively sharp and strong.Furthermore,the purity and crystallinity of the synthesized calcium carboaluminate are higher when heavy CaCO_(3)with the particle size of 120 mesh is used as the carbonate raw material,in comparison to CO_(2),Na_(2)CO_(3)and light CaCO_(3).As results,a simple and efficient method for the synthesis of calcium carboaluminate is proposed,which will provide a solid experimental foundation and technical support for the industrial application of calcium carboaluminate in marine concrete.
基金supported by the National Natural Science Foundation of China (No.52274304)。
文摘The three-dimensional(3D) Pd-based nanoflower structures,assembled from two-dimensional(2D)nanosheets,are characterized by their stable and ordered configurations.These structures have been extensively designed as anode materials for fuel cells.However,the exploration of trimetallic nanoflowers with porous architectures remains limited.In this study,we present a straightforward one-step solvothermal method for the synthesis of trimetallic Pd Cu Ni porous nanoflowers(PNFs).Leveraging several unique advantages,such as an open superstructure,high porosity,and enhanced electronic interactions among the trimetals,the resulting Pd Cu Ni PNFs demonstrate significantly improved electrochemical performance,with mass activities reaching 5.94 and 10.14 A/mg for the ethanol oxidation reaction(EOR)and the ethylene glycol oxidation reaction(EGOR),respectively.Furthermore,the Pd Cu Ni PNFs exhibit optimized d-band centers and the most negative onset oxidation potential,indicating enhanced antitoxicity and stability.This study not only provides a novel perspective on the synthesis of 3D porous nanomaterials but also highlights the potential application value of trimetallic nanoalloys in catalysis.
基金Project (2007J0012) supported by the Natural Science Foundation of Fujian Province, ChinaProject (019811) supported by Foxy in the 6th Framework Program, European Commission
文摘Electrochemical studies on silicon deposition were performed in molten salt electrolytes. Purification of metallurgical grade silicon by electrorefining was carried out in molten Si-chloride salts at temperatures from 973 K to 1223 K. It was found that the use of a liquid alloy anode of silicon and copper was beneficial in molten CaCl2 with NaCl, CaO and dissolved Si. ICP-AES analysis results showed efficient removal of metal impurities, such as titanium, aluminum and iron, which are present in significant quantities in the feedstock. The contents of boron and phosphorus in the silicon after electrorefining were reduced from 36×10-6 and 25×10-6 to 4.6×10-6 and 2.8 ×10-6, respectively. The energy consumption of electrorefining was estimated to be about 9.3 kW?h/kg.
文摘The electrochemical synthesis silicon wires by electrorefining metallurgical grade silicon in thermally dried and pre-electrolyzed molten KF-NaF eutectic were studied at temperatures 800-900 ℃ using cyclic voltammetry and ac impedance. One oxidation peak at -0.14 V could be attributed to the reaction of Si to Si4＋. A cathodic peak occurred at -0.56 V in the cyclic voltammogram and one response semicircle in the ac impedance spectrum was observed, supporting a one-step electrochemical reduction process of Si4＋-→Si. The electrochemical reaction of silicon was controlled by the diffusion process. The purity of electrorefined silicon wires was up to 99.999% by ICP-MS analysis.
基金Supported by the National Natural Science Foundation of China(21676022)the Fundamental Research Funds for the Central Universities(BHYC170A&JD701)
文摘The present paper reports a new fluoride-free and energy-saving lead electrolytic refining process in order to solve the serious problems of the existing Betts lead electrorefining process, such as low production efficiency,high energy consumption and fluorine pollution. In the process, a mixed solution of perchloric acid and lead perchlorate(HClO4-Pb(ClO4)2) with the additives of gelatin and sodium lignin sulfonate is employed as the new electrolyte. The cathodic polarization curves show that HClO4 is very stable, and there is no any reduction reaction of HClO4 during the electrolytic process. The redox reactions of lead ions in HClO4 solution are very reversible with an ultrahigh capacity efficiency, so the HClO4 acts as a stable support electrolyte with higher ionic conductivity than the traditional H2SiF6 electrolyte. The results of the scale-up experiments show that under the optimal conditions of 2.8 mol·L-1 HClO4, 0.4 mol·L-1 Pb(ClO4)2 and electrolysis temperature of 45 ℃, the energy consumption is as low as 24.5 kW·h·(t Pb)-1 , only about 20% of that by Betts method at the same current density of 20 mA·cm-2, and the purity of the refined lead is up to 99.9992%, much higher than that specified by Chinese national standard(99.994%, GB/T 469-2013) and European standard(99.99%, EN 12659–1999).
基金financial supports from the National Natural Science Foundation of China (51634010,51904354)the National Science Fund for Distinguished Young Scholars of China (51825403)+1 种基金the National Key R&D Program of China (2018YFC1900306,2019YFC1907405)Key Research and Development Program of Hunan Province,China (2019SK2291)。
文摘A new hydrometallurgical route for separation and recovery of Cu from Cu-As-bearing copper electrorefining black slime was developed. The proposed process comprised oxidation acid leaching of Cu-As-bearing slime and selective sulfide precipitation of Cu from the leachate. The effects of various process parameters on the leaching and precipitation of Cu and As were investigated. At the first stage, Cu extraction of 95.2% and As extraction of 97.6% were obtained at 80 ℃ after 4 h with initial H2 SO4 concentration of 1.0 mol/L and liquid-to-solid ratio of 10 mL/g. In addition, the leaching kinetics of Cu and As was successfully reproduced by the Avrami model, and the apparent activation energies were found to be 33.6 and 35.1 kJ/mol for the Cu and As leaching reaction, respectively, suggesting a combination of chemical reaction and diffusion control. During the selective sulfide precipitation, about 99.4% Cu was recovered as CuS, while only 0.1% As was precipitated under the optimal conditions using sulfide-to-copper ratio of 2.4:1, time of 1.5 h and temperature of 25 ℃.
基金supported by the National Nature Science Foundation of China(Nos.21601200 and 21771188)Strategic Priority Research Program and Frontier Science Key Program(Nos.XD02030000 and QYZDY-SSW-JSC016)of the Chinese Academy of Sciences
文摘Electrorefining of nickel in LiCl–KCl melt was investigated using electrochemical techniques. Nickel products after electrorefining were characterized by X-ray diffraction, X-ray fluorescence, and scanning electron microscopy. Both cyclic voltammetry and square wave voltammetry results suggested that Ni^2+ was directly reduced to Ni metal in LiCl–KCl. Based on a preliminary study on the electrochemical behavior of nickel and chromium, electrorefining was carried out under constant potential, whereupon deposits were formed on the cathode. The purity of nickel increased from 72.62% in the original alloy to 99.83% in cathodic deposits, as determined by inductively coupled plasma atomic emission spectroscopy analysis. Almost all the nickel in the alloy could be recovered during the electrochemical process with[90% current efficiency. A lower concentration of NiCl2 in LiCl– KCl was found to be favorable for nickel electrorefining, as increased NiCl2 concentration caused severe corrosion of the nickel anode at the gas–liquid interface due to the accumulation of Cl2 gas.
基金Project(LY17B030009)supported by the Natural Science Foundation of Zhejiang Province,China。
文摘A practical approach was introduced to study the inclusion mechanism of chlorine in high purity copper electrorefining from nitric acid system via cyclic voltammetry(CV) combined with electrodeposition experiments. The CV curves display an obvious reduction peak of Cu Cl intermediate, which can provide an insight into the electrochemical behavior of this inclusion. Experimental results show that the increase of HNO3 concentration is favorable to reducing the quantity of chlorine inclusion although there is a slight decline in cathodic current efficiency. The optimum conditions for copper electrorefining in nitric acid system are HNO3 concentration in solution of 1-2 mol/L, moderate temperature of ~35 ℃ with current density not exceeding 25 m A/cm2. Based on the theoretical studies, an optimized copper electrorefining experiment was designed to simulate the industrial electrolysis, by which high purity copper can be obtained with chlorine inclusion less than 10 μg/g and current efficiency higher than 90%.
文摘The application of indium requires high purity indium as material, and the high purity indium has been prepared by electrorefining. The selection and preparation of electrolyte in electrorefining indium were investigated, and the effect of component of electrolytic solution on electrolytic refining was also studied. Compared with electrolyte of InCl3-HCl, electrolyte of In2（SO4）3-H2SO4 has higher stability and lower corrosivity, electrolytic solution can be heated at low temperature, and bath is open and simple, which makes operation more convenient. The results show that the voltage can be kept at 0.30.5 V, and the content of indium can exceed 99.999% when the content of indium（Ⅲ） ion and sodium chloride are 80120 g/L. The bench-scale test of electrolysis was carried out, and the product of indium reaches the national standard of 99.999% high purity indium.
基金Project(52004062)supported by the National Natural Science Foundation of ChinaProject(2020-MS-084)supported by the Natural Science Foundation of Liaoning Province,ChinaProject(N2125014)supported by the Fundamental Research Funds for the Central Universities,China。
文摘The electrochemical behavior of Al(Ⅲ)in urea-1-butyl-3-methylimidazolium chloride-aluminum chloride(urea-BMIC-AlCl_(3))ionic liquids,and the effect of potential and temperature on the characterization of cathode products,current efficiency and energy consumption of aluminum electrorefining have been investigated.Cyclic voltammetry showed that the electrochemical reduction of Al(Ⅲ)was a one-step three-electron-transfer irreversible reaction,and the electrochemical reaction was controlled by diffusion.The diffusion coefficient of Al(Ⅲ)in urea-BMIC-AlCl_(3)ionic liquids at 313 K was 1.94×10^(−7)cm^(2)/s.The 7075 aluminum alloy was used as an anode for electrorefining,and the cathode products were analyzed by XRD,SEM and EDS.The results from XRD analysis indicated that the main phase of the cathode products was aluminum.The results from SEM and EDS characterization revealed that the cathode product obtained by electrorefining−1.2 V(vs.Al)was dense and uniform,and the mass fraction of aluminum decreased from 99.61%to 99.10%as the experimental temperature increased from 313 K to 333 K.In this work,the optimum experimental conditions were−1.2 V(vs.Al)and 313 K.At this time,the cathode current efficiency was 97.80%,while the energy consumption was 3.72 kW·h/kg.
文摘The influences of cupric ion concentration （5-35 g/L）,current density （500-2000 A/m2）,circulation rate of the electrolyte solution （15-120 mL/min）,and temperature （25-60℃） on the physical and chemical properties of copper powders obtained in electrolysis cells were investigated.Two industrial processes,electrorefining （ER） cells with a synthetic electrolyte and electrowinning （EW） cells with an original solution of coppermineral leaching,were utilized to produce copper powders.Finally,the statistical full factorial method of design of experiments （DOE） was employed to investigate the interaction or the main effects of processes.The results show that increasing the copper concentration and temperature can increase the grain size,apparent density,and electrical energy consumption.On the other hand,increasing the current density and circulation rate of the electrolyte can decrease them.This production process is optimized via DOE to control the interactive and main effects to produce copper powders with favorable properties.
基金financially supported by the National Natural Science Foundation of China(No.12304077)the Natural Science Foundation of Science and Technology Department of Sichuan Province(No.23NSFSC6224)+3 种基金Sichuan Science and Technology Program(No.2024NSFSC0989)the Key Laboratory of Computational Physics of Sichuan Province(No.YBUJSWL-YB-2022-03)the Material Corrosion and Protection Key Laboratory of Sichuan Province(No.2023CL14 and No.2023CL01)the National Innovation Practice Project(No.202411079005S).
文摘Oxygen release and electrolyte decomposition under high voltage endlessly exacerbate interfacial ramifications and structu ral degradation of high energy-density Li-rich layered oxide(LLO),leading to voltage and capacity fading.Herein,the dual-strategy of Cr,B complex coating and local gradient doping is simultaneously achieved on LLO surface by a one-step wet chemical reaction at room temperature.Density functional theory(DFT)calculations prove that stable B-O and Cr-O bonds through the local gradient doping can significantly reduce the high-energy O 2p states of interfacial lattice O,which is also effective for the near-surface lattice O,thus greatly stabilizing the LLO surface,Besides,differential electrochemical mass spectrometry(DEMS)indicates that the Cr_(x)B complex coating can adequately inhibit oxygen release and prevents the migration or dissolution of transition metal ions,including allowing speedy Li^(+)migration,The voltage and capacity fading of the modified cathode(LLO-C_(r)B)are adequately suppressed,which are benefited from the uniformly dense cathode electrolyte interface(CEI)composed of balanced organic/inorganic composition.Therefore,the specific capacity of LLO-CrB after 200 cycles at 1C is 209.3 mA h g^(-1)(with a retention rate of 95.1%).This dual-strategy through a one-step wet chemical reaction is expected to be applied in the design and development of other anionic redox cathode materials.
基金supported by Key Research&Development Program of Jiangsu Province in China(BE2020693)Major Project of Science and Technology of Anhui Province(201903a06020010)+1 种基金Joint Key Project of Science and Technology Innovation of Yangtze River Delta in Anhui Province(202004g01020009)the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)。
文摘In this work,one-step growth models using hyperspectral imaging(HSI)(400-1000 nm)were successfully developed in order to estimate the microbial loads,minimum growth temperature(T_(min))and maximum specific growth rate(μ_(max))of Brochothrix thermosphacta in chilled beef at isothermal temperatures(4-25℃).Three different methods were compared for model development,particularly using(Model Ⅰ)the predicted microbial loads from partial least squares regression of the whole spectral variables;(Model Ⅱ)the selected spectral variables related to microbial loads;and(Model Ⅲ)the first principal scores of HSI spectra by principal component analysis.Consequently,Model Ⅰ showed the best ability to predict the microbial loads of B.thermosphacta,with the coefficient of determination(R_(v)^(2))and root mean square error in internal validation(RMSEV)of 0.921 and 0.498(lg(CFU/g)).The T_(min)(-12.32℃)andμmax can be well estimated with R^(2) and root mean square error(RMSE)of 0.971 and 0.276(lg(CFU/g)),respectively.The upward trend ofμmax with temperature was similar to that of the plate count method.HSI technique thus can be used as a simple method for one-step growth simulation of B.thermosphacta in chilled beef during storage.
文摘BACKGROUND Inflammatory bowel disease(IBD)is a common chronic intestinal inflammatory disease.High oxidative stress is a treatment target for IBD.Cerium oxide(CeO2)nanomaterials as nanozymes with antioxidant activity are potential drugs for the treatment of colitis.AIM To synthesize hollow cerium(H-CeO2)nanoparticles by one-step method and to validate the therapeutic efficacy of H-CeO2 in IBD.METHODS H-CeO2 was synthesized by one-step method and examined its characterization and nanoenzymatic activity.Subsequently,we constructed dextran sulfate so-dium(DSS)-induced colitis in mice to observe the effects of H-CeO2 on colonic inflammation.The effects of H-CeO2 on colon inflammation and reactive oxygen species(ROS)levels in IBD mice were detected by hematoxylin and eosin staining and dichlorofluorescein diacetate staining,respectively.Finally,the biological sa-fety of H-CeO2 on mice was evaluated by hematoxylin and eosin staining,blood routine,and blood biochemistry.RESULTS H-CeO2 nanoparticles prepared by the one-step method were uniform,monodi-sperse and hollow.H-CeO2 had a good ability to scavenge ROS,∙OH and∙OOH.H-CeO2 reduced DSS-induced decreases in body weight and colon length,colonic epithelial damage,inflammatory infiltration,and ROS accumulation.H-CeO2 administration reduced the disease activity index of DSS-induced animals from about 8 to 5.H-CeO2 had no significant effect on body weight,total platelet count,hemoglobin,white blood cell,and red blood cell counts in healthy mice.No significant damage to major organs was observed in healthy mice following H-CeO2 administration.CONCLUSION The one-step synthesis of H-CeO2 nanomaterials had good antioxidant activity,biosafety,and inhibited deve-lopment of DSS-induced IBD in mice by scavenging ROS.
基金the Natural Science Foundation of Chongqing of China(Nos.CSTB2024NSCQ-MSX1013 and cstc2021jcyj-msxmX1139)the Science and Technology Research Program of Chongqing Education Commission(Nos.KJZD-K202304502,KJQN202201214,KJQN202001243 and KJZD-M202301201)the Opening Project of Material Corrosion and Protection Key Laboratory of Sichuan province(No.2024CL05).
文摘Building a superhydrophobic coating on a carbon steel substrate is an effective strategy for enhancing metal protection.A practical approach to producing a series of superhydrophobic Ni/SiO_(2)composite coatings(SSN)using one-step electrodeposition method is shown.The effect of processing parameters on surface structure and wettability was thoroughly explored,resulting in the identification of three typical surface morphologies.The prepared coating with petal-like structure(SSN-3)obtained under the optimum parameters exhibited the best water repellency,achieving a contact angle of 162.7°and a sliding angle of 4.1°.The droplet bouncing behavior on SSN coatings surface was studied,and the delayed icing time was recorded.Meanwhile,the mechanical stability and chemical corrosion resistance of SSN coatings were focused.The superhydrophobic SSN-3 coating with unique surface structure exhibited excellent reliability.The anticorrosion mechanism of SSN-3 coating was discussed,and its corrosion protection efficiency was up to 98.5%.The superior properties of the superhydrophobic SSN-3 coating make it suitable for diverse applications.
基金Funded by the Scientific Research Program of Jilin Provincial Science and Technology Development(No.20250203184SF)。
文摘A solid,fast-dissolving sodium silicate was used as an alkaline activator.Granulated blast furnace slag(GGBS),metakaolin(MK),and steel slag(SS)were used as the cementious components to prepare a ternary composite cementitious material known as alkali-activated steel slag composite cementitious material(ASCM)by the"one-step method".The impacts of cementitious components,alkali activator modulus,and Na_(2)O%on the mechanical strength were investigated,and the hydration products and hydration kinetics of ASCM were analyzed.The experimental results reveal that XRD,FTIR,SEM,EDS,and exothermic heat of hydration show that when GGBS:MK:SS=60wt%:10wt%:30wt%,the activator modulus is 1.2,and the alkali content is 5.5wt%,the 28 d flexural strength of ASCM mortar is 12.6 MPa,and the compressive strength is 53.3 MPa,the hydration products consist of C-S-H gel/C-A-S-H gel,mullite(3Al_(2)O_(3)-2SiO_(2)),calcite(CaCO_(3)),quartz,etc.ASCM has a large initial hydration exotherm rate but a small cumulative exotherm.
基金supported by the National Natural Science Foundation of China (No.22275052)Department of Science and Technology of Hubei Province (Nos.2025AFA111 and 2024CSA076)。
文摘The hydrogen evolution reaction(HER) is a key process in electrocatalytic water splitting for hydrogen production,yet it is often limited by sluggish H^(*)-OH adsorption and H*binding kinetics.We obtained Rumodified Ni O nanoparticles(Ru-Ni O/NF) with enhanced HER properties by substituting ruthenium(Ru)for Ni atoms in the Ni O(200) crystalline facets on nickel foam by a one-step electrodeposition technique.This novel catalyst exhibits a significantly reduced H^(*)-OH adsorption energy and improved kinetics,with an overpotential of only 60 mV at 10 mA/cm^(2) and a Tafel slope of 26.19 mV/dec.The Ru-Ni O/NF maintains its activity for over 115 h,outperforming NiO/NF by reducing the overpotential by 177 mV.DFT calculations confirm that the addition of Ru to NiO enhances the HER kinetics by modifying the electronic structure,optimizing the surface chemistry,stabilizing the intermediates,lowering the energy barriers,and facilitating efficient charge transfer through a robust three-dimensional structure,resulting in a change in the rate-limiting step and a significant reduction in the Gibbs free energy.This study presents a highly efficient HER catalyst and offers insights into designing advanced NiO-based electrocatalysts by reducing reaction energy barriers.
基金supported by the National Natural Science Foundation of China (No. 20890111)
文摘The optimal condition for a one-step process removing organic compounds from coking wastewater by simultaneously synthesized organobentonite as a pretreatment was investigated.Results showed that sorption of organic compounds by organobentonite was positively correlated to the cation surfactant exchange on the bentonite and the octanol-water partition coefficient（Kow） of the solutes.With 0.75 g/L bentonite and 180 mg/L（60% of bentonite cation exchange capacity） cetyltrimethylammonium bromide,the removal efficiencies of the 16 polycyclic aromatic hydrocarbon（PAHs） specified by the US Environmental Protection Agency in coking wastewater except naphthalene were more than 90%,and that of benzo（a）pyrene was 99.5%.At the same time,the removal efficiencies of CODCr,NH3-N,volatile phenols,colour and turbidity were 28.6%,13.2%,8.9%,55% and 84.3%,respectively,and the ratio of BOD5/CODCr increased from 0.31 to 0.41.These results indicated that the one-step process had high removal efficiency for toxic and refractory hydrophobic organic compounds,and could improve the biodegradability of the coking wastewater.Therefore it could be a promising technology for the pretreatment of toxic and refractory organic wastewater.
