The leaching process of magnesiothermic self-propagating product generated during the multistage deep reduction process was investigated.The influence of magnesiothermic self-propagating product particle size,HCl solu...The leaching process of magnesiothermic self-propagating product generated during the multistage deep reduction process was investigated.The influence of magnesiothermic self-propagating product particle size,HCl solution concentration,and leaching solution temperature on the leaching behavior of elements Al and V was investigated.Results demonstrate that the leaching rate of Al and V is increased with the rise in leaching solution temperature,the increase in HCl solution concentration,and the enlargement of magnesiothermic self-propagating product particle size.The leaching processes of Al and V are consistent with the chemical reaction control model.When the magnesiothermic self-propagation product with D_(50) of 59.4μm is selected as the raw material,the leaching temperature is 40℃,and 1 mol/L HCl solution is employed,after leaching for 180 min,the leaching rates of Al and V are 24.8%and 12.6%,respectively.The acid-leached product exhibits a porous structure with a specific surface area of 3.5633 m^(2)/g.展开更多
Low-valent sulfur oxy-acid salts(LVSOs)represent a category of oxygen-containing salts characterized by their potent reducing capabilities.Notably,sulfite,dithionite,and thiosulfate are prevalent reducing agents that ...Low-valent sulfur oxy-acid salts(LVSOs)represent a category of oxygen-containing salts characterized by their potent reducing capabilities.Notably,sulfite,dithionite,and thiosulfate are prevalent reducing agents that are readily available,cost-effective,and exhibit minimal ecological toxicity.These LVSOs have the ability to generate or promote the generation of strong oxidants or reductants,which makes them widely used in advanced oxidation processes(AOPs)and advanced reduction processes(ARPs).This article provides a comprehensive review of the recent advancements in AOPs and ARPs involving LVSOs,alongside an examination of the fundamental principles governing the generation of active species within these processes.LVSOs fulfill three primary functions in AOPs:Serving as sources of reactive oxygen species(ROS),auxiliary agents,and activators.Particular attention is devoted to elucidating the reaction mechanisms through which LVSOs,in conjunction with metal ions,metal oxides,ultraviolet light(UV),and ozone,produce potent oxidizing agents in both homogeneous and heterogeneous systems.Regarding ARPs,this review delineates the mechanisms by which LVSOs generate strong reducing agents,including hydrated electrons,hydrogen radicals,and sulfite radicals,under UV irradiation,while also exploring the interactions between these reductants and pollutants.The review identifies existing gaps within the current framework and proposes future research avenues to address these challenges.展开更多
Effects of citrate concentration and pH on the electrochemical reduction process of Co（Ⅱ） were investigated by cyclic voltammetry（CV） and electrochemical impedance spectroscopy（EIS）. The results show that Co（...Effects of citrate concentration and pH on the electrochemical reduction process of Co（Ⅱ） were investigated by cyclic voltammetry（CV） and electrochemical impedance spectroscopy（EIS）. The results show that Co（Ⅱ） is reduced into two species which are free Co2＋ and [Co（C6H607）] in the solution composed of 0.05 mol/L CoS04·5H2O, 0.20 mol/L Na2SO4 and 0-0.40 mol/L C6H5O7Na3·2H2O in the pH range of 3-9. The reduction behavior depends on the pH of the solution. Co（H） is mainly reduced into the form of free Co^2＋ at pH 3 and into the form of [Co（C6H6O7）] at the pH range of 4-6 in citrate solution. The [Co（C6H6O7）] is first reduced to an intermediate state and then to Co°. Adsorption of the intermediate state exists on the surface of the electrode. Co（Ⅱ） is difficult to be reduced in the solution with the pH above 7, because the existing Co（Ⅱ）-citrate complex species [Co（C6H5O7）]- and [Co（C6H4O7）]2- are more difficult to be reduced than the hydrogen ion.展开更多
The degradation of metoprolol(MTP)by the UV/sulfite with oxygen as an advanced reduction process(ARP)and that without oxygen as an advanced oxidation process(AOP)was comparatively studied herein.The degradation of MTP...The degradation of metoprolol(MTP)by the UV/sulfite with oxygen as an advanced reduction process(ARP)and that without oxygen as an advanced oxidation process(AOP)was comparatively studied herein.The degradation of MTP by both processes followed the first-order rate law with comparable reaction rate constants of 1.50×10^(-3)sec^(−1)and 1.20×10^(-3)sec^(−1),respectively.Scavenging experiments demonstrated that both e^(−)_(aq)and H·played a crucial role in MTP degradation by the UV/sulfite as an ARP,while SO_(4)^(·−)was the dominant oxidant in the UV/sulfite AOP.The degradation kinetics of MTP by the UV/sulfite as an ARP and AOP shared a similar pH dependence with a minimum rate obtained around pH 8.The results could be well explained by the pH impacts on the MTP speciation and sulfite species.Totally six transformation products(TPs)were identified from MTP degradation by the UV/sulfite ARP,and two additional ones were detected in the UV/sulfite AOP.The benzene ring and ether groups of MTP were proposed as the major reactive sites for both processes based on molecular orbital calculations by density functional theory(DFT).The similar degradation products of MTP by the UV/sulfite process as an ARP and AOP indicated that e^(−)_(aq)/H·and SO_(4)^(·−)might share similar reaction mechanisms,primarily including hydroxylation,dealkylation,and H abstraction.The toxicity of MTP solution treated by the UV/sulfite AOP was calculated to be higher than that in the ARP by the Ecological Struc-ture Activity Relationships(ECOSAR)software,due to the accumulation of TPs with higher toxicity.展开更多
A one-dimensional unsteady mathematical model was established to describe direct reduction in a composite pellet made of metallurgical dust. The model considered heat transfer, mass transfer, and chemical reactions in...A one-dimensional unsteady mathematical model was established to describe direct reduction in a composite pellet made of metallurgical dust. The model considered heat transfer, mass transfer, and chemical reactions including iron oxide reductions, zinc oxide reduction and carbon gasification, and it was numerically solved by the tridiagonal matrix algorithm （TDMA）. In order to verify the model, an experiment was performed, in which the profiles of temperature and zinc removal rate were measured during the reduction process. Results calculated by the mathematical model were in fairly good agreement with experimental data. Finally, the effects of furnace temperature, pellet size, and carbon content were investigated by model calculations. It is found that the pellet temperature curve can be divided into four parts according to heating rate. Also, the zinc removal rate increases with the increase of furnace temperature and the decrease of pellet size, and carbon content in the pellet has little influence on the zinc removal rate.展开更多
High-concentration nitrite-containing wastewater that presents extreme toxicity to human health and organisms is difficult to be treated using traditional biological process. In this study, a novel microwave-enhanced ...High-concentration nitrite-containing wastewater that presents extreme toxicity to human health and organisms is difficult to be treated using traditional biological process. In this study, a novel microwave-enhanced chemical reduction process （MECRP） using sulfarninic acid （SA） was proposed as a new manner to treat such type of wastewater. Based on lab-scale experiments, it was shown that 75%-80% nitrite （NO2-） could be removed within time as short as 4 min under 50 W microwave irradiation in pH range 5-10 when molar ratio of SA to nitrite （SA/NO2-） was 0.8. Pilot-scale investigations demonstrated that MECRP was able to achieve nitrite and chemical oxygen demand （COD） removal with efficiency up to 80% and 20%, respectively under operating conditions of SA concentration 80 kg/m3, SA/NO2- ratio 0.8, microwave power 3.4 kW, and stirring time 3 min. Five-day biological oxygen demand （BODs）/COD value of treated effluent after MECRP was increased from 0.05 to 0.36 （by 620%）, which clearly suggested a considerable improvement of biodegradability for subsequent biological treatment. This study provided a demonstration of using microwave irradiation to enhance reaction between SA and nitrite in a short time, in which nitrite in wastewater was completely converted into nitrogen gas without leaving any sludge and secondary pollutants.展开更多
Up to now, the Pedgion magnesium reduction process is the dominating magnesium production process. In 2004, about 98% of raw magnesium is produced by Pedgion magnesium reduction process in China which equals to 60% of...Up to now, the Pedgion magnesium reduction process is the dominating magnesium production process. In 2004, about 98% of raw magnesium is produced by Pedgion magnesium reduction process in China which equals to 60% of the global output. It shows that the dolomite-ferrosilicon thermal reduction process is the most important method to produce magnesium in the world. Limited by the disadvantage of dolomite-ferrosilicon thermal reduction process, the magnesium producing process always followed by relatively severe pollution, while the resource utilizing efficiency keeps very low. With the rapid development of dolomite-ferrosilicon thermal reduction process in China, many research works have been done aiming at the process technology and the reduction theory, and the magnesium producing process has got great evolution. The history of dolomite-ferrosilicon thermal reduction process was introduced; the process character, the merits and which defects were also discussed. Defects in dolomite-ferrosilicon thermal reduction process were expatiated, and feasible method and idea to upgrade the process was put forward. The main problems and the potential troubles hindering the development of magnesium industry were analyzed. Finally, the probability to further improve the thermal reduction process and the effective approaches to develop Chinese magnesium industry were discussed.展开更多
Scandia doped tungsten powders were prepared by spray drying combined with two-step hydrogen reduction.The particle size of doped tungsten powder,powder morphology and doped tungsten matrix were characterized by scann...Scandia doped tungsten powders were prepared by spray drying combined with two-step hydrogen reduction.The particle size of doped tungsten powder,powder morphology and doped tungsten matrix were characterized by scanning electron microscope,X-ray diffrac-tion and laser diffraction particle size analyzer,respectively.The reduction behavior of Sc2O3 doped tungsten oxide and the effect of Sc2O3 on the property of tungsten powder were studied by the temperature programmed reduction.The experimental results showed that the pre-cursor powders prepared by spray drying had spherical shape.The addition of Sc2O3 could decrease the reduction temperature of tungsten oxide.The scandia doped tungsten powder had sub-micrometer size in the range of 0.1 to1 μm and scandium distributed evenly in the powder.By using this kind powder,sub-microstructure cathode matrices with semispherical grains and homogenous distribution of scan-dium were obtained.展开更多
Energy saving has been an important concept in modern industry especially to the countries and regions with energy shortage such as China and Japan. Utilization of Coal-Water Slurry （CWS） can improve the burning eff...Energy saving has been an important concept in modern industry especially to the countries and regions with energy shortage such as China and Japan. Utilization of Coal-Water Slurry （CWS） can improve the burning efficiency of coal and reduce the pollutions of soot, sulfide and the nitride by burning lump coal directly. The CWS is a promising energy saving technique and the effectual substitute of oil. The study on the preparation and application of the CWS has made progresses in many aspects. The present paper studied the basal problems for applying the CWS on the rotary kilns during the calcining-dolomite process in the magnesium factory, summarized the key points for the application process of the CWS and gave the corresponding solutions.展开更多
In this study,innovative ellipsoid pellet with craters on its surface was designed,and the direct reduction process was compared with ellipsoid(without craters)and sphere pellets.In addition,furnace temperature and un...In this study,innovative ellipsoid pellet with craters on its surface was designed,and the direct reduction process was compared with ellipsoid(without craters)and sphere pellets.In addition,furnace temperature and uneven heat flux density effects on the pellet direct reduction process were also studied.The results show that ellipsoid pellet is better than that of spherical pellet on metallization ratio.However,under the condition of non-uniform heat flow,the ellipsoid pellet final metallization rate and zinc removal rate were lower.Although the heat transfer effect of ellipsoid pellet with craters was not improved significantly,the metallization rate and zinc removal rate were found improved,which will have a cumulative effect on the pellets direct reduction process in rotary hearth furnace.Under varying furnace temperature conditions,the pellet temperature was higher than that of the constant furnace temperature.After 1200 s,pellet Fe concentration increased to 123.6%,metallization rate and zinc removal rate increased to 113.7%and 102.2%,respectively.These results can provide references for the carbon-containing pellet design used in rotary hearth furnace.展开更多
Magnesium and magnesium alloys,serving as crucial lightweight structural materials and hydrogen storage elements,find extensive applications in space technology,aviation,automotive,and magnesium-based hydrogen industr...Magnesium and magnesium alloys,serving as crucial lightweight structural materials and hydrogen storage elements,find extensive applications in space technology,aviation,automotive,and magnesium-based hydrogen industries.The global production of primary magnesium has reached approximately 1.2 million tons per year,with anticipated diversification in future applications and significant market demand.Nevertheless,approximately 80%of the world’s primary magnesium is still manufactured through the Pidgeon process,grappling with formidable issues including high energy consumption,massive carbon emission,significant resource depletion,and environmental pollution.The implementation of the relative vacuum method shows potential in breaking through technological challenges in the Pidgeon process,facilitating clean,low-carbon continuous magnesium smelting.This paper begins by introducing the principles of the relative vacuum method.Subsequently,it elucidates various innovative process routes,including relative vacuum ferrosilicon reduction,aluminum thermal reduction co-production of spinel,and aluminum thermal reduction co-production of calcium aluminate.Finally,and thermodynamic foundations of the relative vacuum,a quantitative analysis of the material,energy flows,carbon emission,and production cost for several new processes is conducted,comparing and analyzing them against the Pidgeon process.The study findings reveal that,with identical raw materials,the relative vacuum silicon thermal reduction process significantly decreases raw material consumption,energy consumption,and carbon dioxide emissions by 15.86%,30.89%,and 26.27%,respectively,compared to the Pidgeon process.The relative vacuum process,using magnesite as the raw material and aluminum as the reducing agent,has the lowest magnesium-to-feed ratio,at only 3.385.Additionally,its energy consumption and carbon dioxide emissions are the lowest,at 1.817 tce/t Mg and 7.782 t CO_(2)/t Mg,respectively.The energy consumption and carbon emissions of the relative vacuum magnesium smelting process co-producing calcium aluminate(12CaO·7Al_(2)O_(3),3CaO·Al_(2)O_(3),and CaO·Al_(2)O_(3))are highly correlated with the consumption of dolomite in the raw materials.When the reduction temperature is around 1473.15 K,the critical volume fraction of magnesium vapor for different processes varies within the range of 5%–40%.Production cost analysis shows that the relative vacuum primary magnesium smelting process has significant economic benefits.This paper offers essential data support and theoretical guidance for achieving energy efficiency,carbon reduction in magnesium smelting,and the industrial adoption of innovative processes.展开更多
In response to the new mechanism of direct vortex melting reduction of vanadium–titanium magnetite,the reaction control mechanism and the migration regularity of valuable components in the process of direct melting r...In response to the new mechanism of direct vortex melting reduction of vanadium–titanium magnetite,the reaction control mechanism and the migration regularity of valuable components in the process of direct melting reduction were investigated using kinetic empirical equation by fitting and combining with X-ray diffraction,X-ray fluorescence,scanning electron microscopy,energy-dispersive spectrometry,and optical microscopy.The results show that iron reduction is controlled by the mass transfer process of(FeOx)in the slag,while vanadium reduction is controlled by both the mass transfer of(VOx)in the slag and the mass transfer of[V]in the molten iron,and the slag–metal interfacial reaction is the only pathway for vanadium reduction.The reduction of iron and vanadium is an obvious first-order reaction,with activation energy of 101.6051 and 197.416 kJ mol^(−1),respectively.Increasing the vortex rate and reaction temperature is beneficial to improving the reaction rate and reduction efficiency.The mineral phase variation of iron and vanadium in the slag during the reduction process is Fe_(2)O_(3)→Fe_(3)O_(4)/FeV_(2)O_(4)→FeTiO_(3) and FeV_(2)O_(4)→MgV_(2)O_(5);titanium in slag is mainly in the form of Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)and CaTiO_(3).As the reaction time went on,the molar ratio(nTi/nMg)in Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)and the Ti2O_(3) content in the slag gradually went up,while the area proportion of Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)went up and then down,and the porosity of the slag and the grain size of Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)got smaller.展开更多
With the fast development of the application of magnesium based alloys,the demand for primary magnesium is increasing dramatically all over the world.The Pidgeon process is the most widely used process for producing m...With the fast development of the application of magnesium based alloys,the demand for primary magnesium is increasing dramatically all over the world.The Pidgeon process is the most widely used process for producing magnesium in China,but suffers from problems such as high energy,resource consumption and environmental pollution.While the process of vacuum carbothermal reduction to produce magnesium(VCTRM)has attracted more and more attention as its advantages,but it has not been well-practiced in industrial applications and there also is no comprehensive and quantitative analysis of this process.This study quantified the flows of resource and energy for the Pidgeon process and the VCTRM process,then compared and analyzed these two processes with each other from three aspects.The VCTRM process results in 63.14%and 69.16%lower of non-renewable mineral resources and energy consumptions when compared to the Pidgeon process,respectively.Moreover,the low energy consumption(2.675 tce vs.8.681 tce)and material to magnesium ratio(2.953:1 vs.6.429:1)of the VCTRM process,which lead to lower greenhouse gas(GHG)emissions(8.777 t vs.26.337 t)and solid waste generation(0.522 t vs.5.465 t)with a decrease of 66.67%and 90.45%,respectively.Results indicate that the VCTRM process is a more environmentally friendly process for magnesium production with high efficiency but low cost and low pollution,and it shows a good potential to be industrialized in the future after solving the bottleneck problem of the reverse reaction.展开更多
In this study,the environmentally friendly precursor,tartaric acid(TA),was employed for the generation of CO_(2)anion radical(CO_(2)^(·-))in an advanced UV/TA/Fe^(3+)system to reduce the hazardous NO_(2)^(-)-N in...In this study,the environmentally friendly precursor,tartaric acid(TA),was employed for the generation of CO_(2)anion radical(CO_(2)^(·-))in an advanced UV/TA/Fe^(3+)system to reduce the hazardous NO_(2)^(-)-N in wastewater.To optimize this process,various factors,including the dosage of Fe^(3+),TA,and p H,were systematically investigated for their impact on the reduction process.Under the conditions of 3 mmol/L Fe^(3+)dosage,10 mmol/L TA dosage,and a pH of 2.5,NO_(2)^(-)-N was effectively removed from the water within 60 min,selectively transformed into N_(2),with a remarkable N_(2)selectivity of 91.2%.In the optimal conditions,the NO_(2)^(-)-N reduction mechanism in the UV/TA/Fe^(3+)system and the critical role of CO_(2)^(·-)were illustrated.Finally,this study explored the reduction of real nitrified seawater using the UV/TA/Fe^(3+)system.The results demonstrated that the UV/TA/Fe^(3+)system could completely eliminate NO_(2)^(-)-N and achieve a N_(2)selectivity of up to 90%,with minimal interference from coexisting ions.This work holds promising implications for the environmentally benign treatment of nitrite-polluted wastewater.展开更多
Numerical simulations of gas–liquid two-phase flow and alumina transport process in an aluminum reduction cell were conducted to investigate the effects of anode configurations on the bath flow, gas volume fraction a...Numerical simulations of gas–liquid two-phase flow and alumina transport process in an aluminum reduction cell were conducted to investigate the effects of anode configurations on the bath flow, gas volume fraction and alumina content distributions. An Euler–Euler two-fluid model was employed coupled with a species transport equation for alumina content. Three different anode configurations such as anode without a slot, anode with a longitudinal slot and anode with a transversal slot were studied in the simulation. The simulation results clearly show that the slots can reduce the bath velocity and promote the releasing of the anode gas, but can not contribute to the uniformity of the alumina content. Comparisons of the effects between the longitudinal and transversal slots indicate that the longitudinal slot is better in terms of gas–liquid flow but is disadvantageous for alumina mixing and transport process due to a decrease of anode gas under the anode bottom surface. It is demonstrated from the simulations that the mixing and transfer characteristics of alumina are controlled to great extent by the anode gas forces while the electromagnetic forces(EMFs) play the second role.展开更多
The solid-state reduction kinetics of pre-oxidized vanadium-titanium magnetite concentrate was studied. The phase and microstructure of the reduction product were characterized by XRD, SEM and EDS methods, based on wh...The solid-state reduction kinetics of pre-oxidized vanadium-titanium magnetite concentrate was studied. The phase and microstructure of the reduction product were characterized by XRD, SEM and EDS methods, based on which the mechanism of the solid-state reduction was investigated. The results showed that using coal as reductant at 950-1100 °C, the solid-state reduction of the pre-oxidized vanadium-titanium magnetite concentrate was controlled by interface chemical reaction and the apparent activation energy was 67.719 k J/mol. The mineral phase transformation during the reduction process can be described as follows： pre-oxidized vanadium-titanium magnetite concentrate → ulvospinel → ilmenite → Fe Ti2O5 →（FenTi1-n）Ti2O5. M3O5-type（M can be Fe, Ti, Mg, Mn, etc） solid solutions would be formed during the reduction process of the pre-oxidized vanadium-titanium magnetite concentrate at 1050 °C for 60 min. The poor reducibility of iron in M3O5 solid solutions is the main reason to limit the reduction property of pre-oxidized vanadium-titanium magnetite concentrate.展开更多
For the efficient electrolytic extraction of Er from spent nuclear fuel,a series of electrochemical methods was used to research the electrochemical behavior of Er(Ⅲ)in the LiCl—KCl system on inert(Mo)electrode and ...For the efficient electrolytic extraction of Er from spent nuclear fuel,a series of electrochemical methods was used to research the electrochemical behavior of Er(Ⅲ)in the LiCl—KCl system on inert(Mo)electrode and on reactive(Ni)electrodes.On the inert Mo electrode,the reduction of Er(Ⅲ)to Er(0)is a onestep with three-electron and quasi-reversible reaction process.Meanwhile,the apparent generation Gibbs free energy and activity coefficients of Er(Ⅲ)on the inert electrode were determined.Thereafter,the electrochemical reduction of Er(Ⅲ)on the Ni electrode was emphatically investigated.Er(Ⅲ)is reduced at a corrected potential owing to the formation of Ni-Er alloys.In addition,thermodynamic parameters such as partial excess Gibbs free energy change of Er in Ni,activity and apparent generation Gibbs free energy of the Ni-Er alloys were determined by the electromotive force method.Finally,different Ni-Er alloys were produced using potentiostatic electrolysis on the Ni cathode by controlling different potentials,Moreover,electrolytic extraction was carried out on the Ni cathode at the potential of-2.0 V,and the separation efficiency of Er reaches 99.72%,which proves the practicability of separating Er from LiCl-KCl eutectic on the reactive Ni cathode.展开更多
The persistence of chlorinated alkanes in aquatic environments poses significant health risks due to its biotoxicity and high volatility,which contributes to both water and air pollution.This study investigates the ef...The persistence of chlorinated alkanes in aquatic environments poses significant health risks due to its biotoxicity and high volatility,which contributes to both water and air pollution.This study investigates the efficacy of carbon dioxide radical anion(CO_(2)·^(-))mediated advanced reduction processes(ARPs)for the reductive dechlorination of chlorinated alkanes using small molecular monocarboxylic acids(SMAs)under UV irradiation.The study focused on formic acid(HCOOH),acetic acid(CH_3COOH),and propionic acid(CH_3CH_(2)COOH)to generate CO_(2)·^(-),revealing that UV/HCOOH system exhibits a notably high chloroform(CF)degradation efficiency of 97.8%in 90 min.Kinetic studies indicated a linear relationship between the HCOOH concentrations and the observed reaction rate constants(k_(obs)),demonstrating that CO_(2)·^(-)production is crucial for CF degradation.Electron paramagnetic resonance spectroscopy identified CO_(2)·^(-)and hydroxyl radicals(HO·)as the active species,with the former playing a predominant role in CF degradation.The study also explored the influence of carbon chain length in SMAs on CF degradation,finding that longer chains decrease the degradation efficiency,potentially due to reduced UV activation.A higher reaction rate constant(k_(obs))under acidic conditions,with a marked decrease in efficiency as the pH exceeds 3.7,where HCOO^(-)becomes predominant.This study enhances our understanding of CO_(2)·^(-)mediated ARPs and explores potential applications in environmental remediation,providing insights into the pathways and mechanisms of CF degradation.The UV/SMAs systems offer advantages for practical applications,such as milder reaction conditions and higher efficiency compared to traditional methods.展开更多
A mathematical model was established to describe the direct reduction of pellets in a rotary hearth furnace （RHF）. In the model, heat transfer, mass transfer, and gas-solid chemical reactions were taken into account...A mathematical model was established to describe the direct reduction of pellets in a rotary hearth furnace （RHF）. In the model, heat transfer, mass transfer, and gas-solid chemical reactions were taken into account. The behaviors of iron metallization and dezincification were analyzed by the numerical method, which was validated by experimental data of the direct reduction of pellets in a Si-Mo furnace. The simulation results show that if the production targets of iron metallization and dezincification are up to 80% and 90%, respectively, the furnace temperature for high-temperature sections must be set higher than 1300~ C. Moreover, an undersupply of secondary air by 20% will lead to a decline in iron metallization rate of discharged pellets by 10% and a decrease in dezincing rate by 13%. In addition, if the residence time of pellets in the furnace is over 20 min, its further extension will hardly lead to an obvious increase in production indexes under the same furnace temperature curve.展开更多
Basic physicochemical properties of the dust from Laiwu Iron and Steel Co. Ltd. were studied. It is found that C, Zn, K, Na, etc. exist in the fabric filter dust, off gas （OG） sludge, fine ash in converter, and elec...Basic physicochemical properties of the dust from Laiwu Iron and Steel Co. Ltd. were studied. It is found that C, Zn, K, Na, etc. exist in the fabric filter dust, off gas （OG） sludge, fine ash in converter, and electrical field dust in sinter. Among these, OG sludge gives the finest particle, more than 90% of which is less than 2.51 mm. The dust can lead to a serious negative influence on the production of sintering and blast furnaces （BF） if it is recycled in sintering. The briquette and reduction experimental results showed that the qualified strength could be obtained in the case of 8wt% molasses or 4wt% QT-10 added as binders. Also, more than 75% of metallization ratio, more than 95% of dezincing ratio, as well as more than 80% of K and Na removal rates were achieved for the briquettes kept at 1250℃ for 15 min during the direct reduction process. SEM observation indicated that the rates of indirect reduction and carbonization became dominating when the bri-quettes were kept at 1250℃ for 6 min.展开更多
基金Scientific and Technological Project of Nanyang(23KJGG017)Key Specialized Research&Development and Promotion Project(Scientific and Technological Project)of Henan Province(232102221022)+1 种基金College Students and Technology Innovation Fund Project of Nanyang Institute of Technology(2023139)Project of Doctoral Scientific Research Startup Fund of Nanyang Institute of Technology(NGBJ-2023-25)。
文摘The leaching process of magnesiothermic self-propagating product generated during the multistage deep reduction process was investigated.The influence of magnesiothermic self-propagating product particle size,HCl solution concentration,and leaching solution temperature on the leaching behavior of elements Al and V was investigated.Results demonstrate that the leaching rate of Al and V is increased with the rise in leaching solution temperature,the increase in HCl solution concentration,and the enlargement of magnesiothermic self-propagating product particle size.The leaching processes of Al and V are consistent with the chemical reaction control model.When the magnesiothermic self-propagation product with D_(50) of 59.4μm is selected as the raw material,the leaching temperature is 40℃,and 1 mol/L HCl solution is employed,after leaching for 180 min,the leaching rates of Al and V are 24.8%and 12.6%,respectively.The acid-leached product exhibits a porous structure with a specific surface area of 3.5633 m^(2)/g.
基金supported by Natural Science Foundation of China(Nos.52070133,42107073,42477075)Natural Science Foundation of Sichuan Province(No.2024NSFSC0130)+2 种基金the Sichuan Science and Technology Program(No.2024NSFTD0014)Key Laboratory of Jiangxi Province for Persistent Pollutants Prevention Control and Resource Reuse(No.2023SSY02061)Key R&D Program of Heilongjiang Province(No.2023ZX02C01)。
文摘Low-valent sulfur oxy-acid salts(LVSOs)represent a category of oxygen-containing salts characterized by their potent reducing capabilities.Notably,sulfite,dithionite,and thiosulfate are prevalent reducing agents that are readily available,cost-effective,and exhibit minimal ecological toxicity.These LVSOs have the ability to generate or promote the generation of strong oxidants or reductants,which makes them widely used in advanced oxidation processes(AOPs)and advanced reduction processes(ARPs).This article provides a comprehensive review of the recent advancements in AOPs and ARPs involving LVSOs,alongside an examination of the fundamental principles governing the generation of active species within these processes.LVSOs fulfill three primary functions in AOPs:Serving as sources of reactive oxygen species(ROS),auxiliary agents,and activators.Particular attention is devoted to elucidating the reaction mechanisms through which LVSOs,in conjunction with metal ions,metal oxides,ultraviolet light(UV),and ozone,produce potent oxidizing agents in both homogeneous and heterogeneous systems.Regarding ARPs,this review delineates the mechanisms by which LVSOs generate strong reducing agents,including hydrated electrons,hydrogen radicals,and sulfite radicals,under UV irradiation,while also exploring the interactions between these reductants and pollutants.The review identifies existing gaps within the current framework and proposes future research avenues to address these challenges.
基金Project(200800560002)supported by the Ph.D.Programs Foundation of Ministry of Education of China
文摘Effects of citrate concentration and pH on the electrochemical reduction process of Co（Ⅱ） were investigated by cyclic voltammetry（CV） and electrochemical impedance spectroscopy（EIS）. The results show that Co（Ⅱ） is reduced into two species which are free Co2＋ and [Co（C6H607）] in the solution composed of 0.05 mol/L CoS04·5H2O, 0.20 mol/L Na2SO4 and 0-0.40 mol/L C6H5O7Na3·2H2O in the pH range of 3-9. The reduction behavior depends on the pH of the solution. Co（H） is mainly reduced into the form of free Co^2＋ at pH 3 and into the form of [Co（C6H6O7）] at the pH range of 4-6 in citrate solution. The [Co（C6H6O7）] is first reduced to an intermediate state and then to Co°. Adsorption of the intermediate state exists on the surface of the electrode. Co（Ⅱ） is difficult to be reduced in the solution with the pH above 7, because the existing Co（Ⅱ）-citrate complex species [Co（C6H5O7）]- and [Co（C6H4O7）]2- are more difficult to be reduced than the hydrogen ion.
基金This study was supported by the Guangdong introducing innovative and entrepreneurial teams(No.2019ZT08L213)the Key Special Project for Introduced Talents Team of Southern Marine Science and Engineering Guangdong Laboratory(Guangzhou)(No.GML2019ZD0403)+2 种基金the National Natural Science Foundation of China(Nos.51979044 and 42177045)the Young Talent Project of Beijing Normal University at Zhuhai(No.310432101)We also thank the support received from China Scholarship Council(CSC)for providing a graduate fellowship to Y.C.(No.202006120356).
文摘The degradation of metoprolol(MTP)by the UV/sulfite with oxygen as an advanced reduction process(ARP)and that without oxygen as an advanced oxidation process(AOP)was comparatively studied herein.The degradation of MTP by both processes followed the first-order rate law with comparable reaction rate constants of 1.50×10^(-3)sec^(−1)and 1.20×10^(-3)sec^(−1),respectively.Scavenging experiments demonstrated that both e^(−)_(aq)and H·played a crucial role in MTP degradation by the UV/sulfite as an ARP,while SO_(4)^(·−)was the dominant oxidant in the UV/sulfite AOP.The degradation kinetics of MTP by the UV/sulfite as an ARP and AOP shared a similar pH dependence with a minimum rate obtained around pH 8.The results could be well explained by the pH impacts on the MTP speciation and sulfite species.Totally six transformation products(TPs)were identified from MTP degradation by the UV/sulfite ARP,and two additional ones were detected in the UV/sulfite AOP.The benzene ring and ether groups of MTP were proposed as the major reactive sites for both processes based on molecular orbital calculations by density functional theory(DFT).The similar degradation products of MTP by the UV/sulfite process as an ARP and AOP indicated that e^(−)_(aq)/H·and SO_(4)^(·−)might share similar reaction mechanisms,primarily including hydroxylation,dealkylation,and H abstraction.The toxicity of MTP solution treated by the UV/sulfite AOP was calculated to be higher than that in the ARP by the Ecological Struc-ture Activity Relationships(ECOSAR)software,due to the accumulation of TPs with higher toxicity.
基金the Fundamen-tal Research Funds for Central Universities(No.FRF-SD-12-013A)the State Key Laboratory of Advanced Metallurgy,China
文摘A one-dimensional unsteady mathematical model was established to describe direct reduction in a composite pellet made of metallurgical dust. The model considered heat transfer, mass transfer, and chemical reactions including iron oxide reductions, zinc oxide reduction and carbon gasification, and it was numerically solved by the tridiagonal matrix algorithm （TDMA）. In order to verify the model, an experiment was performed, in which the profiles of temperature and zinc removal rate were measured during the reduction process. Results calculated by the mathematical model were in fairly good agreement with experimental data. Finally, the effects of furnace temperature, pellet size, and carbon content were investigated by model calculations. It is found that the pellet temperature curve can be divided into four parts according to heating rate. Also, the zinc removal rate increases with the increase of furnace temperature and the decrease of pellet size, and carbon content in the pellet has little influence on the zinc removal rate.
基金supported by the National Natural Science Foundation of China (No.50678045)
文摘High-concentration nitrite-containing wastewater that presents extreme toxicity to human health and organisms is difficult to be treated using traditional biological process. In this study, a novel microwave-enhanced chemical reduction process （MECRP） using sulfarninic acid （SA） was proposed as a new manner to treat such type of wastewater. Based on lab-scale experiments, it was shown that 75%-80% nitrite （NO2-） could be removed within time as short as 4 min under 50 W microwave irradiation in pH range 5-10 when molar ratio of SA to nitrite （SA/NO2-） was 0.8. Pilot-scale investigations demonstrated that MECRP was able to achieve nitrite and chemical oxygen demand （COD） removal with efficiency up to 80% and 20%, respectively under operating conditions of SA concentration 80 kg/m3, SA/NO2- ratio 0.8, microwave power 3.4 kW, and stirring time 3 min. Five-day biological oxygen demand （BODs）/COD value of treated effluent after MECRP was increased from 0.05 to 0.36 （by 620%）, which clearly suggested a considerable improvement of biodegradability for subsequent biological treatment. This study provided a demonstration of using microwave irradiation to enhance reaction between SA and nitrite in a short time, in which nitrite in wastewater was completely converted into nitrogen gas without leaving any sludge and secondary pollutants.
文摘Up to now, the Pedgion magnesium reduction process is the dominating magnesium production process. In 2004, about 98% of raw magnesium is produced by Pedgion magnesium reduction process in China which equals to 60% of the global output. It shows that the dolomite-ferrosilicon thermal reduction process is the most important method to produce magnesium in the world. Limited by the disadvantage of dolomite-ferrosilicon thermal reduction process, the magnesium producing process always followed by relatively severe pollution, while the resource utilizing efficiency keeps very low. With the rapid development of dolomite-ferrosilicon thermal reduction process in China, many research works have been done aiming at the process technology and the reduction theory, and the magnesium producing process has got great evolution. The history of dolomite-ferrosilicon thermal reduction process was introduced; the process character, the merits and which defects were also discussed. Defects in dolomite-ferrosilicon thermal reduction process were expatiated, and feasible method and idea to upgrade the process was put forward. The main problems and the potential troubles hindering the development of magnesium industry were analyzed. Finally, the probability to further improve the thermal reduction process and the effective approaches to develop Chinese magnesium industry were discussed.
基金Project supported by Beijing Natural Science Foundation (2102007)Program for Excellent Talents in Beijing (PHR201006101)National Nature Science funding (51071005)
文摘Scandia doped tungsten powders were prepared by spray drying combined with two-step hydrogen reduction.The particle size of doped tungsten powder,powder morphology and doped tungsten matrix were characterized by scanning electron microscope,X-ray diffrac-tion and laser diffraction particle size analyzer,respectively.The reduction behavior of Sc2O3 doped tungsten oxide and the effect of Sc2O3 on the property of tungsten powder were studied by the temperature programmed reduction.The experimental results showed that the pre-cursor powders prepared by spray drying had spherical shape.The addition of Sc2O3 could decrease the reduction temperature of tungsten oxide.The scandia doped tungsten powder had sub-micrometer size in the range of 0.1 to1 μm and scandium distributed evenly in the powder.By using this kind powder,sub-microstructure cathode matrices with semispherical grains and homogenous distribution of scan-dium were obtained.
文摘Energy saving has been an important concept in modern industry especially to the countries and regions with energy shortage such as China and Japan. Utilization of Coal-Water Slurry （CWS） can improve the burning efficiency of coal and reduce the pollutions of soot, sulfide and the nitride by burning lump coal directly. The CWS is a promising energy saving technique and the effectual substitute of oil. The study on the preparation and application of the CWS has made progresses in many aspects. The present paper studied the basal problems for applying the CWS on the rotary kilns during the calcining-dolomite process in the magnesium factory, summarized the key points for the application process of the CWS and gave the corresponding solutions.
基金Project(cstc 2018 jszx-cyzdx 0100)supported by the Chongqing Technology Innovation and Application Demonstration Project,China。
文摘In this study,innovative ellipsoid pellet with craters on its surface was designed,and the direct reduction process was compared with ellipsoid(without craters)and sphere pellets.In addition,furnace temperature and uneven heat flux density effects on the pellet direct reduction process were also studied.The results show that ellipsoid pellet is better than that of spherical pellet on metallization ratio.However,under the condition of non-uniform heat flow,the ellipsoid pellet final metallization rate and zinc removal rate were lower.Although the heat transfer effect of ellipsoid pellet with craters was not improved significantly,the metallization rate and zinc removal rate were found improved,which will have a cumulative effect on the pellets direct reduction process in rotary hearth furnace.Under varying furnace temperature conditions,the pellet temperature was higher than that of the constant furnace temperature.After 1200 s,pellet Fe concentration increased to 123.6%,metallization rate and zinc removal rate increased to 113.7%and 102.2%,respectively.These results can provide references for the carbon-containing pellet design used in rotary hearth furnace.
基金supported by the China Postdoctoral Science Foundation(No.2023T160088)the Youth Fund of the National Natural Science Foundation of China(No.52304324).
文摘Magnesium and magnesium alloys,serving as crucial lightweight structural materials and hydrogen storage elements,find extensive applications in space technology,aviation,automotive,and magnesium-based hydrogen industries.The global production of primary magnesium has reached approximately 1.2 million tons per year,with anticipated diversification in future applications and significant market demand.Nevertheless,approximately 80%of the world’s primary magnesium is still manufactured through the Pidgeon process,grappling with formidable issues including high energy consumption,massive carbon emission,significant resource depletion,and environmental pollution.The implementation of the relative vacuum method shows potential in breaking through technological challenges in the Pidgeon process,facilitating clean,low-carbon continuous magnesium smelting.This paper begins by introducing the principles of the relative vacuum method.Subsequently,it elucidates various innovative process routes,including relative vacuum ferrosilicon reduction,aluminum thermal reduction co-production of spinel,and aluminum thermal reduction co-production of calcium aluminate.Finally,and thermodynamic foundations of the relative vacuum,a quantitative analysis of the material,energy flows,carbon emission,and production cost for several new processes is conducted,comparing and analyzing them against the Pidgeon process.The study findings reveal that,with identical raw materials,the relative vacuum silicon thermal reduction process significantly decreases raw material consumption,energy consumption,and carbon dioxide emissions by 15.86%,30.89%,and 26.27%,respectively,compared to the Pidgeon process.The relative vacuum process,using magnesite as the raw material and aluminum as the reducing agent,has the lowest magnesium-to-feed ratio,at only 3.385.Additionally,its energy consumption and carbon dioxide emissions are the lowest,at 1.817 tce/t Mg and 7.782 t CO_(2)/t Mg,respectively.The energy consumption and carbon emissions of the relative vacuum magnesium smelting process co-producing calcium aluminate(12CaO·7Al_(2)O_(3),3CaO·Al_(2)O_(3),and CaO·Al_(2)O_(3))are highly correlated with the consumption of dolomite in the raw materials.When the reduction temperature is around 1473.15 K,the critical volume fraction of magnesium vapor for different processes varies within the range of 5%–40%.Production cost analysis shows that the relative vacuum primary magnesium smelting process has significant economic benefits.This paper offers essential data support and theoretical guidance for achieving energy efficiency,carbon reduction in magnesium smelting,and the industrial adoption of innovative processes.
基金supported by the National Natural Science Foundation of China(U1908225)the Fundamental Research Funds for Central Universities(N2225012 and N232405-06).
文摘In response to the new mechanism of direct vortex melting reduction of vanadium–titanium magnetite,the reaction control mechanism and the migration regularity of valuable components in the process of direct melting reduction were investigated using kinetic empirical equation by fitting and combining with X-ray diffraction,X-ray fluorescence,scanning electron microscopy,energy-dispersive spectrometry,and optical microscopy.The results show that iron reduction is controlled by the mass transfer process of(FeOx)in the slag,while vanadium reduction is controlled by both the mass transfer of(VOx)in the slag and the mass transfer of[V]in the molten iron,and the slag–metal interfacial reaction is the only pathway for vanadium reduction.The reduction of iron and vanadium is an obvious first-order reaction,with activation energy of 101.6051 and 197.416 kJ mol^(−1),respectively.Increasing the vortex rate and reaction temperature is beneficial to improving the reaction rate and reduction efficiency.The mineral phase variation of iron and vanadium in the slag during the reduction process is Fe_(2)O_(3)→Fe_(3)O_(4)/FeV_(2)O_(4)→FeTiO_(3) and FeV_(2)O_(4)→MgV_(2)O_(5);titanium in slag is mainly in the form of Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)and CaTiO_(3).As the reaction time went on,the molar ratio(nTi/nMg)in Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)and the Ti2O_(3) content in the slag gradually went up,while the area proportion of Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)went up and then down,and the porosity of the slag and the grain size of Mg_(x)Ti_(3−x)O_(5)(0≤x≤1)got smaller.
基金the Yunnan Ten Thousand Talents Plan Industrial Technology Champion Project Foundation of China(No.YNWR-CYJS-2018-015)Basic Research Project of Yunnan Province(No.2019FB080).
文摘With the fast development of the application of magnesium based alloys,the demand for primary magnesium is increasing dramatically all over the world.The Pidgeon process is the most widely used process for producing magnesium in China,but suffers from problems such as high energy,resource consumption and environmental pollution.While the process of vacuum carbothermal reduction to produce magnesium(VCTRM)has attracted more and more attention as its advantages,but it has not been well-practiced in industrial applications and there also is no comprehensive and quantitative analysis of this process.This study quantified the flows of resource and energy for the Pidgeon process and the VCTRM process,then compared and analyzed these two processes with each other from three aspects.The VCTRM process results in 63.14%and 69.16%lower of non-renewable mineral resources and energy consumptions when compared to the Pidgeon process,respectively.Moreover,the low energy consumption(2.675 tce vs.8.681 tce)and material to magnesium ratio(2.953:1 vs.6.429:1)of the VCTRM process,which lead to lower greenhouse gas(GHG)emissions(8.777 t vs.26.337 t)and solid waste generation(0.522 t vs.5.465 t)with a decrease of 66.67%and 90.45%,respectively.Results indicate that the VCTRM process is a more environmentally friendly process for magnesium production with high efficiency but low cost and low pollution,and it shows a good potential to be industrialized in the future after solving the bottleneck problem of the reverse reaction.
基金financially supported by National Natural Science Foundation of China(No.22208081)Central Guidance on Local Science and Technology Development Fund of Hebei Province(No.226Z3102G)Fundamental Research Funds of Hebei University of Technology(No.JBKYTD2001)。
文摘In this study,the environmentally friendly precursor,tartaric acid(TA),was employed for the generation of CO_(2)anion radical(CO_(2)^(·-))in an advanced UV/TA/Fe^(3+)system to reduce the hazardous NO_(2)^(-)-N in wastewater.To optimize this process,various factors,including the dosage of Fe^(3+),TA,and p H,were systematically investigated for their impact on the reduction process.Under the conditions of 3 mmol/L Fe^(3+)dosage,10 mmol/L TA dosage,and a pH of 2.5,NO_(2)^(-)-N was effectively removed from the water within 60 min,selectively transformed into N_(2),with a remarkable N_(2)selectivity of 91.2%.In the optimal conditions,the NO_(2)^(-)-N reduction mechanism in the UV/TA/Fe^(3+)system and the critical role of CO_(2)^(·-)were illustrated.Finally,this study explored the reduction of real nitrified seawater using the UV/TA/Fe^(3+)system.The results demonstrated that the UV/TA/Fe^(3+)system could completely eliminate NO_(2)^(-)-N and achieve a N_(2)selectivity of up to 90%,with minimal interference from coexisting ions.This work holds promising implications for the environmentally benign treatment of nitrite-polluted wastewater.
基金Project(2010AA065201)supported by the High Technology Research and Development Program of ChinaProject(2013zzts038)supported by the Fundamental Research Funds for the Central Universities of ChinaProject(ZB2011CBBCe1)supported by the Major Program for Aluminum Corporation of China Limited,China
文摘Numerical simulations of gas–liquid two-phase flow and alumina transport process in an aluminum reduction cell were conducted to investigate the effects of anode configurations on the bath flow, gas volume fraction and alumina content distributions. An Euler–Euler two-fluid model was employed coupled with a species transport equation for alumina content. Three different anode configurations such as anode without a slot, anode with a longitudinal slot and anode with a transversal slot were studied in the simulation. The simulation results clearly show that the slots can reduce the bath velocity and promote the releasing of the anode gas, but can not contribute to the uniformity of the alumina content. Comparisons of the effects between the longitudinal and transversal slots indicate that the longitudinal slot is better in terms of gas–liquid flow but is disadvantageous for alumina mixing and transport process due to a decrease of anode gas under the anode bottom surface. It is demonstrated from the simulations that the mixing and transfer characteristics of alumina are controlled to great extent by the anode gas forces while the electromagnetic forces(EMFs) play the second role.
基金Project(NCET-10-0834)supported by the Program for New Century Excellent Talents in University,China
文摘The solid-state reduction kinetics of pre-oxidized vanadium-titanium magnetite concentrate was studied. The phase and microstructure of the reduction product were characterized by XRD, SEM and EDS methods, based on which the mechanism of the solid-state reduction was investigated. The results showed that using coal as reductant at 950-1100 °C, the solid-state reduction of the pre-oxidized vanadium-titanium magnetite concentrate was controlled by interface chemical reaction and the apparent activation energy was 67.719 k J/mol. The mineral phase transformation during the reduction process can be described as follows： pre-oxidized vanadium-titanium magnetite concentrate → ulvospinel → ilmenite → Fe Ti2O5 →（FenTi1-n）Ti2O5. M3O5-type（M can be Fe, Ti, Mg, Mn, etc） solid solutions would be formed during the reduction process of the pre-oxidized vanadium-titanium magnetite concentrate at 1050 °C for 60 min. The poor reducibility of iron in M3O5 solid solutions is the main reason to limit the reduction property of pre-oxidized vanadium-titanium magnetite concentrate.
基金Project supported by Ph.D.Student Research and Innovation Fund of the Fundamental Research Funds for the Central Universities(3072023GIP1005)。
文摘For the efficient electrolytic extraction of Er from spent nuclear fuel,a series of electrochemical methods was used to research the electrochemical behavior of Er(Ⅲ)in the LiCl—KCl system on inert(Mo)electrode and on reactive(Ni)electrodes.On the inert Mo electrode,the reduction of Er(Ⅲ)to Er(0)is a onestep with three-electron and quasi-reversible reaction process.Meanwhile,the apparent generation Gibbs free energy and activity coefficients of Er(Ⅲ)on the inert electrode were determined.Thereafter,the electrochemical reduction of Er(Ⅲ)on the Ni electrode was emphatically investigated.Er(Ⅲ)is reduced at a corrected potential owing to the formation of Ni-Er alloys.In addition,thermodynamic parameters such as partial excess Gibbs free energy change of Er in Ni,activity and apparent generation Gibbs free energy of the Ni-Er alloys were determined by the electromotive force method.Finally,different Ni-Er alloys were produced using potentiostatic electrolysis on the Ni cathode by controlling different potentials,Moreover,electrolytic extraction was carried out on the Ni cathode at the potential of-2.0 V,and the separation efficiency of Er reaches 99.72%,which proves the practicability of separating Er from LiCl-KCl eutectic on the reactive Ni cathode.
基金supported by the National Natural Science Foundation of China(Nos.52270165 and 51978537)the Key Laboratory of Safety for Geotechnical and Structural Engineering of Hubei Province。
文摘The persistence of chlorinated alkanes in aquatic environments poses significant health risks due to its biotoxicity and high volatility,which contributes to both water and air pollution.This study investigates the efficacy of carbon dioxide radical anion(CO_(2)·^(-))mediated advanced reduction processes(ARPs)for the reductive dechlorination of chlorinated alkanes using small molecular monocarboxylic acids(SMAs)under UV irradiation.The study focused on formic acid(HCOOH),acetic acid(CH_3COOH),and propionic acid(CH_3CH_(2)COOH)to generate CO_(2)·^(-),revealing that UV/HCOOH system exhibits a notably high chloroform(CF)degradation efficiency of 97.8%in 90 min.Kinetic studies indicated a linear relationship between the HCOOH concentrations and the observed reaction rate constants(k_(obs)),demonstrating that CO_(2)·^(-)production is crucial for CF degradation.Electron paramagnetic resonance spectroscopy identified CO_(2)·^(-)and hydroxyl radicals(HO·)as the active species,with the former playing a predominant role in CF degradation.The study also explored the influence of carbon chain length in SMAs on CF degradation,finding that longer chains decrease the degradation efficiency,potentially due to reduced UV activation.A higher reaction rate constant(k_(obs))under acidic conditions,with a marked decrease in efficiency as the pH exceeds 3.7,where HCOO^(-)becomes predominant.This study enhances our understanding of CO_(2)·^(-)mediated ARPs and explores potential applications in environmental remediation,providing insights into the pathways and mechanisms of CF degradation.The UV/SMAs systems offer advantages for practical applications,such as milder reaction conditions and higher efficiency compared to traditional methods.
基金financially supported by the National Key Basic Research and Development Program of China(No. 2012CB720405)
文摘A mathematical model was established to describe the direct reduction of pellets in a rotary hearth furnace （RHF）. In the model, heat transfer, mass transfer, and gas-solid chemical reactions were taken into account. The behaviors of iron metallization and dezincification were analyzed by the numerical method, which was validated by experimental data of the direct reduction of pellets in a Si-Mo furnace. The simulation results show that if the production targets of iron metallization and dezincification are up to 80% and 90%, respectively, the furnace temperature for high-temperature sections must be set higher than 1300~ C. Moreover, an undersupply of secondary air by 20% will lead to a decline in iron metallization rate of discharged pellets by 10% and a decrease in dezincing rate by 13%. In addition, if the residence time of pellets in the furnace is over 20 min, its further extension will hardly lead to an obvious increase in production indexes under the same furnace temperature curve.
文摘Basic physicochemical properties of the dust from Laiwu Iron and Steel Co. Ltd. were studied. It is found that C, Zn, K, Na, etc. exist in the fabric filter dust, off gas （OG） sludge, fine ash in converter, and electrical field dust in sinter. Among these, OG sludge gives the finest particle, more than 90% of which is less than 2.51 mm. The dust can lead to a serious negative influence on the production of sintering and blast furnaces （BF） if it is recycled in sintering. The briquette and reduction experimental results showed that the qualified strength could be obtained in the case of 8wt% molasses or 4wt% QT-10 added as binders. Also, more than 75% of metallization ratio, more than 95% of dezincing ratio, as well as more than 80% of K and Na removal rates were achieved for the briquettes kept at 1250℃ for 15 min during the direct reduction process. SEM observation indicated that the rates of indirect reduction and carbonization became dominating when the bri-quettes were kept at 1250℃ for 6 min.
