In recent years,biochar(BC)as a low-cost,easily available biomass product,is widely applied in sulfate radical-based advanced oxidation processes(SR-AOPs)for emerging pollutants remediation.Herein,a state-of-art revie...In recent years,biochar(BC)as a low-cost,easily available biomass product,is widely applied in sulfate radical-based advanced oxidation processes(SR-AOPs)for emerging pollutants remediation.Herein,a state-of-art review of iron-based biochar catalysts is currently available in SR-AOPs application.A general summary of the development of biochar and the catalytic properties of biochar is presented.Especially,the synthetic strategies of different types of iron-based biochar catalysts are discussed.Moreover,the theoretical calculation to interpret the interaction between biochar and iron species is discussed to explore the activation mechanisms.And the regeneration methods of biochar-based catalyst are presented.The unresolved challenges of the existent biochar-based SR-AOPs are pointed out,and the outlooks of future research directions are proposed.展开更多
Chlorite(ClO_(2)^(−)or COI)is used to establish the advanced reduction and oxidation process(AROP).The iron/biochar-based particles(iron-based hydrothermal carbon with hinge-like structure,FebHCs,20 mg/L)can be utiliz...Chlorite(ClO_(2)^(−)or COI)is used to establish the advanced reduction and oxidation process(AROP).The iron/biochar-based particles(iron-based hydrothermal carbon with hinge-like structure,FebHCs,20 mg/L)can be utilized to activate COI(2 mmol/L)to present selective oxidation in removing triphenylmethane derivatives(15 min,90%).The protonation(H+at~102μmol/L level)played a huge role(k-2nd=0.136c-H+−0.014(R^(2)-adj=0.986),and rapp=−0.0876/c-H++1.017(R^(2)-adj=0.996))to boost the generation of the active species(e.g.,high-valent iron oxidizing species(HVI=O)and chlorine dioxide(ClO_(2))).The protonation-coupled electron transfer promoted Fe-substances in Feb/HCs activating COI(the calculated kobs ranging from 0.066−0.285 min^(−1)).The form of ClO_(2) mainly attributed to proton-coupled electron transfer(1e/1H+).The HVI=O was generated from the electron transfer within the coordination complex.Moreover,carbon particles in FebHCs serve as the bridge for electron transfer.The above roles contribute to the fracture and formation of coordination-induced bonds between Lx-FeII/III and ClO_(2)^(−)at phase interface to form AROP.The ultrasonic(US)cavitation enhanced the mass transfer of active species in bulk solution,and the HVI=O and ClO_(2) attack unsaturated central carbon atoms of triphenylmethane derivatives to initiate selective removal.Furthermore,the scale-up experiment with continuous flow(k values of approximately 0.2 min^(−1),COD removal efficiency of approximately 80%)and the reactor with COMSOL simulation have also proved the applicability of the system.The study offers a novel AROP and new insights into correspondingly heterogeneous interface activation mechanisms.展开更多
Iron-based metal matrix composites(IMMCs)have attracted significant research attention due to their high specific stiffness and strength,making them potentially suitable for various engineering applications.Microstruc...Iron-based metal matrix composites(IMMCs)have attracted significant research attention due to their high specific stiffness and strength,making them potentially suitable for various engineering applications.Microstructural design,including the selection of reinforcement and matrix phases,the reinforcement volume fraction,and the interface issues are essential factors determining the engineering performance of IMMCs.A variety of fabrication methods have been developed to manufacture IMMCs in recent years.This paper reviews the recent advances and development of IMMCs with particular focus on microstructure design,fabrication methods,and their engineering performance.The microstructure design issues of IMMC are firstly discussed,including the reinforcement and matrix phase selection criteria,interface geometry and characteristics,and the bonding mechanism.The fabrication methods,including liquid state,solid state,and gas-mixing processing are comprehensively reviewed and compared.The engineering performance of IMMCs in terms of elastic modulus,hardness and wear resistance,tensile and fracture behavior is reviewed.Finally,the current challenges of the IMMCs are highlighted,followed by the discussion and outlook of the future research directions of IMMCs.展开更多
We report the crystal growth of a new hole-doped iron-based superconductor Ba(Fe_(0.875)Ti_(0.125))_(2)As_(2)by substituting Ti on the Fe site.The crystals are accidentally obtained in trying to grow Ni doped Ba_(2)Ti...We report the crystal growth of a new hole-doped iron-based superconductor Ba(Fe_(0.875)Ti_(0.125))_(2)As_(2)by substituting Ti on the Fe site.The crystals are accidentally obtained in trying to grow Ni doped Ba_(2)Ti_(2)Fe_(2)As_(4)O.After annealing at 500℃ in vacuum for one week,superconductivity is observed with zero resistance at T_(c0)≈17.5 K,and about 20%diamagnetic volume down to 2 K.While both the small anisotropy of superconductivity and the temperature dependence of normal state resistivity are akin to the electron doped 122-type compounds,the Hall coefficient is positive and similar to the case in hole-doped Ba_(0.9)K_(0.1)Fe_(2)As2.The density functional theory calculations suggest dominated hole pockets contributed by Fe/Ti 3d orbitals.Therefore,the Ba(Fe_(1-x)Ti_(x))_(2)As_(2)system provides a new platform to study the superconductivity with hole doping on the Fe site of iron-based superconductors.展开更多
Specialized vanadium(V)-iron(Fe)-based alloy additives utilized in the production of V-containing steels were investigated.Vanadium slag from the Panzhihua region of China was utilized as a raw material to optimize pr...Specialized vanadium(V)-iron(Fe)-based alloy additives utilized in the production of V-containing steels were investigated.Vanadium slag from the Panzhihua region of China was utilized as a raw material to optimize process parameters for the preparation of V-Fe-based alloy via silicon thermal reduction.Experiments were conducted to investigate the effects of reduction temperature,holding time,and slag composition on alloy-slag separation,alloy microstructure,and the oxide content of residual slag,with an emphasis on the recovery of valuable metal elements.The results indicated that the optimal process conditions for silicon thermal reduction were achieved at reduction temperature of 1823 K,holding time of 240 min,and slag composition of 45 wt.%SiO_(2),40 wt.%CaO,and 15 wt.%Al_(2)O_(3).The resulting V-Fe-based alloy predominantly consisted of Fe-based phases such as Fe,titanium(Ti),silicon(Si)and manganese(Mn),with Si,V,as well as chromium(Cr)concentrated in the intercrystalline phase of the Fe-based alloy.The recoveries of Fe,Mn,Cr,V,and Ti under the optimal conditions were 96.30%,91.96%,86.53%,80.29%,and 74.82%,respectively.The key components of the V-Fe-based alloy obtained were 41.96 wt.%Si,27.55 wt.%Fe,12.13 wt.%Mn,5.53 wt.%V,4.86 wt.%Cr,and 3.74 wt.%Ti,thereby enabling the comprehensive recovery of the valuable metal from vanadium slag.展开更多
Coal-direct chemical looping(CDCL) is a promising CO_(2) capture technology with low costs.Potassium modification can significantly enhance the reactivity of iron-based oxygen carriers and coal.However,potassium loss ...Coal-direct chemical looping(CDCL) is a promising CO_(2) capture technology with low costs.Potassium modification can significantly enhance the reactivity of iron-based oxygen carriers and coal.However,potassium loss causes a decline in cyclic stability.To address this,we prepared a potassium hexatitanate-modified iron-based OC and conducted CDCL experiments in a fixed-bed reactor using Zhundong coal coke as fuel.The study examined the impact of potassium hexatitanate on carbon conversion,OC activity stability,and potassium maintenance.Additionally,Fact Sage was used to calculate potassium fugacity patterns at different temperatures,Fe_(2)O_(3)/C molar ratios,and OC reduction degrees.Results showed that potassium hexatitanate increased carbon conversion,achieving 50%conversion at 40% potassium addition.In multi-cycle tests,carbon conversion rose with increased cycle times,reaching 84%.This improvement is attributed to ion exchange between Fe^(3+) and Ti^(4+),which induces lattice distortion and creates oxygen vacancies,enhancing OC reactivity.Potassium content remained stable during multi-cycle tests,indicating the effective potassium retention capacity of potassium hexatitanate.展开更多
Economical and sustainable wastewater treatment techniques are highly demanded to alleviate the issues of clearwater scarcity globally.In this work,the acetic acid/H_(2)O_(2) (AHP) was leveraged to enrich oxygenated f...Economical and sustainable wastewater treatment techniques are highly demanded to alleviate the issues of clearwater scarcity globally.In this work,the acetic acid/H_(2)O_(2) (AHP) was leveraged to enrich oxygenated functional groups on the biochar surface for efficient ciprofloxacin (CIP) adsorption and biochar regeneration (In situ degradation of CIP in the spent AHP solution).The AHP-modified biochar exhibited significantly enhanced CIP adsorption capacity,about 22 times that of the pristine biochar.The optimized modification condition (acetic acid/H_(2)O_(2):2.11,temperature:45 ℃,and time:12 h) was screened by the response surface method,reaching the highest CIP adsorption capacity of 86.26 mg·g^(−1).Characterization results revealed that the content of carboxyl —C=O—O was enhanced in AHP-modified biochar,which contributed to efficient CIP adsorption by the electrostatic interaction,hydrogen bonding,and hydrophobic interaction.The adsorption of modified biochar to CIP molecules was a spontaneous endothermic process,and in line with the pseudo-second-order model and the Langmuir isotherm model.Moreover,the biochar modification process enabled the spent AHP solution with a strong oxidizing agent of peracetic acid (PAA),which can be employed to degrade adsorbed CIP for biochar in-situ generation.This work tailored a closed-loop strategy for biochar oxidation,contaminant adsorption,and biochar regeneration,highlighting a viable route for sustainable wastewater treatment.展开更多
Flubendiamide is a commonly used pesticide with low water solubility and a high organic carbon sorption constant,causing it to adhere to soil particles and negatively impact soil ecosystems.First,chili plant stems,typ...Flubendiamide is a commonly used pesticide with low water solubility and a high organic carbon sorption constant,causing it to adhere to soil particles and negatively impact soil ecosystems.First,chili plant stems,typically discarded after the harvest season,represent an abundant local biomass resource with significant potential for utilization,and were converted into biochar through pyrolysis.Here,we describe the synthesis of biochar modified with iron and chitosan to increase the diversity of functions and surface functional groups of biochar.The resulting chitosan-modified magnetic biochar(CMBC)presents a full range of functional groups of chitosan and iron oxide as shown by Fourier-transform infrared spectroscopy.The correlation between flubendiamide concentration and the dose of biochar on adsorption was explored.The flubendiamide adsorption efficiency of CMBC(1%mass ratio of soil)reached 68.03%in 90 min.The highest adsorption capacity achieved was 0.95 mg·g^(−1).The flubendiamide adsorption mechanism by CMBC can be described with a pseudo-second-order kinetic model.The experiment data closely fit a Freundlich isotherm model(R^(2)=0.998),and the low residual sum of squares values demonstrate the high model applicability.In this study,we present a comprehensive overview of pesticides,alongside kinetic and isotherm model studies of flubendiamide adsorption by CMBC.We emphasize the potential of modified biochar to enhance environmental remediation applications.展开更多
Biochar and biochar composites are versatile materials that can be used in many applications.In this study,biochar was prepared from sawdust and combined with the yttrium iron garnet(YIG)nanocrystal to investigate the...Biochar and biochar composites are versatile materials that can be used in many applications.In this study,biochar was prepared from sawdust and combined with the yttrium iron garnet(YIG)nanocrystal to investigate the shielding effectiveness of the composite structure.Firstly,the effect of the pyrolysis temperature on the shielding effectiveness of biochar was investigated.Secondly,biochars combined with YIG nanocrystals with different contents and shielding effectiveness of the composites were investigated.The electromagnetic effectiveness of the samples was investigated within the X band(8-12 GHz).The findings indicate that biochar demonstrates enhanced absorption properties with elevated pyrolysis temperatures.Biochars demonstrated an approximate 40 d B shielding effectiveness,while YIG exhibited approximately 7 d B,corresponding to absorption at 8 GHz.However,the combination of biochar and YIG exhibited exceptional absorption,reaching 67.12 d B at 8 GHz.展开更多
In this study,Palm kernel shell(PKS)is utilized as a raw material to produce activated biochar as adsorbent for dye removal from wastewater,specifically methylene blue(MB)dye,by utilizing a simplified and costeffectiv...In this study,Palm kernel shell(PKS)is utilized as a raw material to produce activated biochar as adsorbent for dye removal from wastewater,specifically methylene blue(MB)dye,by utilizing a simplified and costeffective approach.Production of activated biocharwas carried out using both a furnace and a domesticmicrowave oven without an inert atmosphere.Three samples of palm kernel shell(PKS)based activated biochar labeled as samples A,B and C were carbonized inside the furnace at 800℃ for 1 h and then activated using the microwave-heating technique with varying heating times(0,5,10,and 15 min).The heating was conducted in the absence of an inert gas.Fourier Transform Infrared Spectroscopy(FTIR)highlighted a significant Si-O stretching vibration between 1040.5 to 692.7 cm−1,indicating the presence of key components(Silica and Alumina)in all PKS-based activated biochar samples.For wastewater treatment,activated biochar samples were tested against a 20 mg/LMethylene Blue(MB)solution,and the MB percentage removal was calculated for each run using a standard curve.Central Composite Design(CCD)experiments were conducted for optimization,with activated biochar Sample C exhibiting the highest adsorption capacity at 88.14%MB removal under specific conditions.ANOVA analysis confirmed the significance of the quadratic model,with a p-value of 0.0222 and R^(2)=0.9438.In conclusion,the results demonstrated the efficiency of PKS-based activated biochar as an adsorbent for MB removal in comparison to other commercial adsorbents.展开更多
Biochar has been widely recognized as a promising solid CO_(2)adsorbent with economic and ecological benefits.Industrial CO_(2)emissions originate from diverse sources,while the pore structure and chemical functional ...Biochar has been widely recognized as a promising solid CO_(2)adsorbent with economic and ecological benefits.Industrial CO_(2)emissions originate from diverse sources,while the pore structure and chemical functional groups of biochar exhibit varying degrees of influence on CO_(2)adsorption and separation performance under different adsorption conditions.Therefore,exploring the matching relationship between the physicochemical properties of biochar and its adsorption and separation performance at different adsorption conditions is essential for the development and optimization of carbon-based adsorbents.This study selected the high-performance extreme gradient boosting(XGB)algorithm from various algorithms and utilized it to develop CO_(2),N_(2),CH_(4)adsorption prediction models.Based on this,coupled prediction models were developed for CO_(2)/N_(2)and CO_(2)/CH_(4)adsorption selectivity.Furthermore,feature importance and partial dependence analysis were performed using SHAP values.The results indicate that during CO_(2)adsorption,the influence of the pore structure of biochar outweighs that of its chemical composition.Specifically,the pore structure of 0.4–0.6 nm is the most important property influencing CO_(2)adsorption at low and medium pressure(0–0.6 bar),and the pore structure of 0.6–0.8 nm,as well as the specific surface area contribute the most at high pressure(0.6–1 bar).During CO_(2)selective separation,the CO_(2)/N_(2)mixture is primarily separated through the selective adsorption of CO_(2)by nitrogen functional groups.In contrast,for CO_(2)/CH_(4)mixtures,pore structure<1 nm plays a more critical role in determining adsorption selectivity.In addition,molecular simulation studies further revealed the adsorption filling mechanisms of CO_(2)molecules within different pore sizes and functional groups.Finally,nitrogen-doped biochar was synthesized using de-alkalize lignin as the precursor,KOH as the activating agent,and urea as the nitrogen dopant.CO_(2),N_(2),and CH_(4)isothermal adsorption experiments were conducted,and the experimental results confirmed that the developed prediction models exhibit high accuracy(R^(2)>0.9).展开更多
Developing green and efficient methods to acquire lignocellulose-based chemicals with high added value is beneficial for facilitating green chemistry and sustainable development.The goal of this study is to demonstrat...Developing green and efficient methods to acquire lignocellulose-based chemicals with high added value is beneficial for facilitating green chemistry and sustainable development.The goal of this study is to demonstrate that bio-based benzaldehyde,a noteworthy high-value chemical,is able to be directionally prepared from lignocellulosic biomass.This new control-lable transformation was materialized by uniting catalytic-pyrolysis of lignocellulose to toluene intermediate and catalytic oxidation of toluene intermediate to bio-based benzalde-hyde.This work also developed a highly active magnetic catalyst(CoFe_(2)O_(4)@Biochar(HTR)),achieving 77.1%benzaldehyde selectivity and 46.7%benzaldehyde yield using this catalyst.It was found that introducing the biochar carrier into the cobalt iron composite metal oxide cat-alyst enhanced hydroxyl radical formation and bio-based benzaldehyde synthesis.Based on catalyst characterizations and hydroxyl radical analysis,potential reaction mechanism for bio-based benzaldehyde synthesis was proposed.This strategy may provide a beneficial pathway for developing high-value bio-based chemical(benzaldehyde)using renewable lignocellulosic biomass.展开更多
A systematic study was undertaken to investigate the effects of the manganese incorporation manner on the textural properties, bulk and surface phase compositions, reduction/carburization behaviors, and surface basici...A systematic study was undertaken to investigate the effects of the manganese incorporation manner on the textural properties, bulk and surface phase compositions, reduction/carburization behaviors, and surface basicity of an iron-based Fischer-Tropsch synthesis （FTS） catalyst. The catalyst samples were characterized by N2 physisorption, X-ray photoelectron spectroscopy （XPS）, H2 （or CO） temperature-programmed reduction （TPR）, CO2 temperature-programmed desorption （TPD）, and M5ssbauer spectroscopy. The FTS performance of the catalysts was studied in a slurry-phase continuously stirred tank reactor （CSTR）. The characterization results indicated that the manganese promoter incorporated by using the coprecipitation method could improve the dispersion of iron oxide, and decrease the size of the iron oxide crystallite. The manganese incorporated with the impregnation method is enriched on the catalyst＇s surface. The manganese promoter added with the impregnation method suppresses the reduction and carburization of the catalyst in H2, CO, and syngas because of the excessive enrichment of manganese on the catalyst surface. The catalyst added manganese using the coprecipitation method has the highest CO conversion （51.9%） and the lowest selectivity for heavy hydrocarbons （C12＋）.展开更多
Increasing environmental pollution and shortage of conventional fossil fuels have made it urgent to develop renewable and clean energy sources. Electrocatalytic water splitting, with its abundant raw materials, simple...Increasing environmental pollution and shortage of conventional fossil fuels have made it urgent to develop renewable and clean energy sources. Electrocatalytic water splitting, with its abundant raw materials, simple process, and zero carbon emission, is considered one of the most promising processes for producing carbon-neutral hydrogen which has excellent energy conversion efficiency and high gravimetric energy density. Among them, oxygen evolution reaction (OER) electrocatalysts and hydrogen evolution reaction (HER) electrocatalysts are critical to decreasing the intrinsic reaction energy barrier and boosting the hydrogen evolution efficiency. Therefore, it is imperative to develop and design low-cost, highly active, and stable OER and HER electrocatalysts to lower the overpotential and drive the electrocatalytic reactions. Transition metal sulfides, especially iron-based sulfides, have attracted extensive exploration by researchers as a result of its high abundance in the Earth's crust and near-metallic conductivity. Consequently, in this review, we systematically and comprehensively summarize the progress in the application of iron-based sulfides and their composites as OER and HER electrocatalysts in electrocatalysis. Detailed descriptions and illustrations of the special relationships among their composition, structure, and electrocatalytic performance are presented. Finally, this review points out the challenges and future prospects of iron-based sulfides in practical applications for designing and fabricating more promising iron-based sulfide OER and HER electrocatalysts. We believe that iron-based sulfide materials will have a wide range of application prospects as OER and HER electrocatalysts in the future.展开更多
SiC magnetic abrasive is used to polish surfaces of precise,complex parts which are hard,brittle and highly corrosion-resistant in magnetic abrasive finishing(MAF).Various techniques are employed to produce this magne...SiC magnetic abrasive is used to polish surfaces of precise,complex parts which are hard,brittle and highly corrosion-resistant in magnetic abrasive finishing(MAF).Various techniques are employed to produce this magnetic abrasive,but few can meet production demands because they are usually time-consuming,complex with high cost,and the magnetic abrasives made by these techniques have irregular shape and low bonding strength that result in low processing efficiency and shorter service life.Therefore,an attempt is made by combining gas atomization and rapid solidification to fabricate a new iron-based SiC spherical composite magnetic abrasive.The experimental system to prepare this new magnetic abrasive is constructed according to the characteristics of gas atomization and rapid solidification process and the performance requirements of magnetic abrasive.The new iron-based SiC spherical composite magnetic abrasive is prepared successfully when the machining parameters and the composition proportion of the raw materials are controlled properly.Its morphology,microstructure,phase composition are characterized by scanning electron microscope(SEM)and X-ray diffraction(XRD)analysis.The MAF tests on plate of mold steel S136 are carried out without grinding lubricant to assess the finishing performance and service life of this new SiC magnetic abrasive.The surface roughness(Ra)of the plate worked is rapidly reduced to 0.051μm from an initial value of 0.372μm within 5 min.The MAF test is carried on to find that the service life of this new SiC magnetic abrasive reaches to 155 min.The results indicate that this process presented is feasible to prepare the new SiC magnetic abrasive;and compared with previous magnetic abrasives,the new SiC spherical composite magnetic abrasive has excellent finishing performance,high processing efficiency and longer service life.The presented method to fabricate magnetic abrasive through gas atomization and rapid solidification presented can significantly improve the finishing performance and service life of magnetic abrasive,and provide a more practical approach for large-scale industrial production of magnetic abrasive.展开更多
The heterogeneous Fenton reaction can generate highly reactive hydroxyl radicals（·OH）from reactions between recyclable solid catalysts and H2O2 at acidic or even circumneutral pH.Hence,it can effectively oxidiz...The heterogeneous Fenton reaction can generate highly reactive hydroxyl radicals（·OH）from reactions between recyclable solid catalysts and H2O2 at acidic or even circumneutral pH.Hence,it can effectively oxidize refractory organics in water or soils and has become a promising environmentally friendly treatment technology.Due to the complex reaction system,the mechanism behind heterogeneous Fenton reactions remains unresolved but fascinating,and is crucial for understanding Fenton chemistry and the development and application of efficient heterogeneous Fenton technologies.Iron-based materials usually possess high catalytic activity,low cost,negligible toxicity and easy recovery,and are a superior type of heterogeneous Fenton catalysts.Therefore,this article reviews the fundamental but important interfacial mechanisms of heterogeneous Fenton reactions catalyzed by iron-based materials..OH,hydroperoxyl radicals/superoxide anions（HO2./O2^-.）and high-valent iron are the three main types of reactive oxygen species（ROS）,with different oxidation reactivity and selectivity.Based on the mechanisms of ROS generation,the interfacial mechanisms of heterogeneous Fenton systems can be classified as the homogeneous Fenton mechanism induced by surface-leached iron,the heterogeneous catalysis mechanism,and the heterogeneous reaction-induced homogeneous mechanism.Different heterogeneous Fenton systems catalyzed by characteristic iron-based materials are comprehensively reviewed.Finally,related future research directions are also suggested.展开更多
A series of iron-based Fischer-Tropsch synthesis （FTS） catalysts incorporated with Al2O3 binder were prepared by the combination of co-precipitation and spray drying technology. The catalyst samples were characteriz...A series of iron-based Fischer-Tropsch synthesis （FTS） catalysts incorporated with Al2O3 binder were prepared by the combination of co-precipitation and spray drying technology. The catalyst samples were characterized by using N2 physical adsorption, temperature-programmed reduction/desorption （TPR/TPD） and MSssbauer effect spectroscopy （MES） methods. The characterization results indicated that the BET surface area increases with increasing Al2O3 content and passes through a maximum at the Al2O3/Fe ratio of 10/100 （weight basis）. After the point, it decreases with further increase in Al2O3 content. The incorporation of Al2O3 binder was found to weaken the surface basicity and suppress the reduction and carburization of iron-based catalysts probably due to the strong K-Al2O3 and Fe-Al2O3 interactions. Furthermore, the H2 adsorption ability of the catalysts is enhanced with increasing Al2O3 content. The FTS performances of the catalysts were tested in a slurry-phase continuously stirred tank reactor （CSTR） under the reaction conditions of 260 ℃, 1.5 MPa, 1000 h^-1 and molar ratio of H2/CO 0.67 for 200 h. The results showed that the addition of small amounts of Al2O3 affects the activity of iron-based catalysts to a little extent. However, with further increase of Al2O3 content, the FTS activity and water gas shift reaction （WGS） activity are decreased severely. The addition of appropriate Al2O3 do not affect the product selectivity, but the catalysts incorporated with large amounts of Al2O3 have higher selectivity for light hydrocarbons and lower selectivity for heavy hydrocarbons.展开更多
Although single-pulse lasers are often used in traditional laser-induced breakdown spectroscopy （LIBS） measurements, their measurement outcomes are generally undesirable because of the low sensitivity of carbon in i...Although single-pulse lasers are often used in traditional laser-induced breakdown spectroscopy （LIBS） measurements, their measurement outcomes are generally undesirable because of the low sensitivity of carbon in iron-based alloys. In this article, a double-pulse laser was applied to improve the signal intensity of carbon. Both the inter-pulse delay and the combination of laser wavelengths in double-pulse laser-induced breakdown spectroscopy （DP-LIBS） were optimized in our experiment. At the optimized inter-pulse delay, the combination of a first laser of 532 nm and a second laser of 1,064 nm achieved the highest signal enhancement. The properties of the target also played a role in determining the mass ablation enhancement in DP-LIBS configuration.展开更多
The second class of high-temperature superconductors （HTSCs）, iron-based pnictides and chalcogenides, necessarily contain Fe2X2 （＂X＂ refers to a pnictogen or a chalcogen element） layers, just like the first clas...The second class of high-temperature superconductors （HTSCs）, iron-based pnictides and chalcogenides, necessarily contain Fe2X2 （＂X＂ refers to a pnictogen or a chalcogen element） layers, just like the first class of HTSCs which possess the essential CuO2 sheets. So far, dozens of iron-based HTSCs, classified into nine groups, have been discovered. In this article, the crystal-chemistry aspects of the known iron-based superconductors are reviewed and summarized by employing ＂hard and soft acids and bases （HSAB）＂ concept. Based on these understandings, we propose an alternative route to exploring new iron-based superconductors via rational structural design.展开更多
Between the two major arsenic-containing salts in natural water, arsenite(As(Ⅲ)) is far more harmful to human and the environment than arsenate(As(V)) due to its high toxicity and transportability. Therefore, preoxid...Between the two major arsenic-containing salts in natural water, arsenite(As(Ⅲ)) is far more harmful to human and the environment than arsenate(As(V)) due to its high toxicity and transportability. Therefore, preoxidation of As(Ⅲ) to As(V) is considered to be an effective means to reduce the toxicity of arsenic and to promote the removal efficiency of arsenic. Due to their high catalytic activity and arsenic affinity, iron-based functional materials can quickly oxidize As(Ⅲ) to As(V) in heterogeneous Fenton-like systems, and then remove As(V) from water through adsorption and surface coprecipitation. In this review, the effects of different iron-based functional materials such as zero-valent iron and iron(hydroxy) oxides on arsenic removal are compared, and the catalytic oxidation mechanism of As(Ⅲ) in heterogeneous Fenton process is further clarified. Finally, the main challenges and opportunities faced by iron-based As(Ⅲ) oxidation functional materials are prospected.展开更多
基金supported by the National Natural Science Foundation of China(No.51778230).
文摘In recent years,biochar(BC)as a low-cost,easily available biomass product,is widely applied in sulfate radical-based advanced oxidation processes(SR-AOPs)for emerging pollutants remediation.Herein,a state-of-art review of iron-based biochar catalysts is currently available in SR-AOPs application.A general summary of the development of biochar and the catalytic properties of biochar is presented.Especially,the synthetic strategies of different types of iron-based biochar catalysts are discussed.Moreover,the theoretical calculation to interpret the interaction between biochar and iron species is discussed to explore the activation mechanisms.And the regeneration methods of biochar-based catalyst are presented.The unresolved challenges of the existent biochar-based SR-AOPs are pointed out,and the outlooks of future research directions are proposed.
基金supported by the Natural Science foundation of the Jiangsu Higher Education Institutions(No.24KJB610019)the Scientific Research Foundation of Yancheng Teachers University(No.204060047)the Horizontal Topic Research“Developing the environmental remediation technology by acoustic catalysis”(No.203060199).
文摘Chlorite(ClO_(2)^(−)or COI)is used to establish the advanced reduction and oxidation process(AROP).The iron/biochar-based particles(iron-based hydrothermal carbon with hinge-like structure,FebHCs,20 mg/L)can be utilized to activate COI(2 mmol/L)to present selective oxidation in removing triphenylmethane derivatives(15 min,90%).The protonation(H+at~102μmol/L level)played a huge role(k-2nd=0.136c-H+−0.014(R^(2)-adj=0.986),and rapp=−0.0876/c-H++1.017(R^(2)-adj=0.996))to boost the generation of the active species(e.g.,high-valent iron oxidizing species(HVI=O)and chlorine dioxide(ClO_(2))).The protonation-coupled electron transfer promoted Fe-substances in Feb/HCs activating COI(the calculated kobs ranging from 0.066−0.285 min^(−1)).The form of ClO_(2) mainly attributed to proton-coupled electron transfer(1e/1H+).The HVI=O was generated from the electron transfer within the coordination complex.Moreover,carbon particles in FebHCs serve as the bridge for electron transfer.The above roles contribute to the fracture and formation of coordination-induced bonds between Lx-FeII/III and ClO_(2)^(−)at phase interface to form AROP.The ultrasonic(US)cavitation enhanced the mass transfer of active species in bulk solution,and the HVI=O and ClO_(2) attack unsaturated central carbon atoms of triphenylmethane derivatives to initiate selective removal.Furthermore,the scale-up experiment with continuous flow(k values of approximately 0.2 min^(−1),COD removal efficiency of approximately 80%)and the reactor with COMSOL simulation have also proved the applicability of the system.The study offers a novel AROP and new insights into correspondingly heterogeneous interface activation mechanisms.
基金funding support from the National Natural Science Foundation of China(No.52101046)Shuangjie Chu appreciates the funding support from the National Key Research and Development Program of China(No.2022YFB3705600).
文摘Iron-based metal matrix composites(IMMCs)have attracted significant research attention due to their high specific stiffness and strength,making them potentially suitable for various engineering applications.Microstructural design,including the selection of reinforcement and matrix phases,the reinforcement volume fraction,and the interface issues are essential factors determining the engineering performance of IMMCs.A variety of fabrication methods have been developed to manufacture IMMCs in recent years.This paper reviews the recent advances and development of IMMCs with particular focus on microstructure design,fabrication methods,and their engineering performance.The microstructure design issues of IMMC are firstly discussed,including the reinforcement and matrix phase selection criteria,interface geometry and characteristics,and the bonding mechanism.The fabrication methods,including liquid state,solid state,and gas-mixing processing are comprehensively reviewed and compared.The engineering performance of IMMCs in terms of elastic modulus,hardness and wear resistance,tensile and fracture behavior is reviewed.Finally,the current challenges of the IMMCs are highlighted,followed by the discussion and outlook of the future research directions of IMMCs.
基金supported by the National Key R&D Program of China(Grant Nos.2023YFA1406100,2022YFA1403800,2022YFA1403400,and 2021YFA1400400)the National Natural Science Foundation of China(Grant Nos.12274444 and 12574165)+1 种基金the Chinese Academy of Sciences(Grant No.XDB25000000)financial support from HBNI-RRCAT。
文摘We report the crystal growth of a new hole-doped iron-based superconductor Ba(Fe_(0.875)Ti_(0.125))_(2)As_(2)by substituting Ti on the Fe site.The crystals are accidentally obtained in trying to grow Ni doped Ba_(2)Ti_(2)Fe_(2)As_(4)O.After annealing at 500℃ in vacuum for one week,superconductivity is observed with zero resistance at T_(c0)≈17.5 K,and about 20%diamagnetic volume down to 2 K.While both the small anisotropy of superconductivity and the temperature dependence of normal state resistivity are akin to the electron doped 122-type compounds,the Hall coefficient is positive and similar to the case in hole-doped Ba_(0.9)K_(0.1)Fe_(2)As2.The density functional theory calculations suggest dominated hole pockets contributed by Fe/Ti 3d orbitals.Therefore,the Ba(Fe_(1-x)Ti_(x))_(2)As_(2)system provides a new platform to study the superconductivity with hole doping on the Fe site of iron-based superconductors.
基金the financial support provided by the National Key R&D Program of China(Grant No.2023YFC3903900)the Science and Technology Innovation Talent Program of Hubei Province(Grant No.2022EJD002)+1 种基金the Sichuan Science and Technology Program(Grant No.2025ZNSFSC0378)the Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education(Grant No.LZJ2303).
文摘Specialized vanadium(V)-iron(Fe)-based alloy additives utilized in the production of V-containing steels were investigated.Vanadium slag from the Panzhihua region of China was utilized as a raw material to optimize process parameters for the preparation of V-Fe-based alloy via silicon thermal reduction.Experiments were conducted to investigate the effects of reduction temperature,holding time,and slag composition on alloy-slag separation,alloy microstructure,and the oxide content of residual slag,with an emphasis on the recovery of valuable metal elements.The results indicated that the optimal process conditions for silicon thermal reduction were achieved at reduction temperature of 1823 K,holding time of 240 min,and slag composition of 45 wt.%SiO_(2),40 wt.%CaO,and 15 wt.%Al_(2)O_(3).The resulting V-Fe-based alloy predominantly consisted of Fe-based phases such as Fe,titanium(Ti),silicon(Si)and manganese(Mn),with Si,V,as well as chromium(Cr)concentrated in the intercrystalline phase of the Fe-based alloy.The recoveries of Fe,Mn,Cr,V,and Ti under the optimal conditions were 96.30%,91.96%,86.53%,80.29%,and 74.82%,respectively.The key components of the V-Fe-based alloy obtained were 41.96 wt.%Si,27.55 wt.%Fe,12.13 wt.%Mn,5.53 wt.%V,4.86 wt.%Cr,and 3.74 wt.%Ti,thereby enabling the comprehensive recovery of the valuable metal from vanadium slag.
基金fnancially supported by the Open Research Fund Program of Anhui Provincial Institute of Modern Coal Processing Technology,Anhui University of Science and Technology (MTY202201)。
文摘Coal-direct chemical looping(CDCL) is a promising CO_(2) capture technology with low costs.Potassium modification can significantly enhance the reactivity of iron-based oxygen carriers and coal.However,potassium loss causes a decline in cyclic stability.To address this,we prepared a potassium hexatitanate-modified iron-based OC and conducted CDCL experiments in a fixed-bed reactor using Zhundong coal coke as fuel.The study examined the impact of potassium hexatitanate on carbon conversion,OC activity stability,and potassium maintenance.Additionally,Fact Sage was used to calculate potassium fugacity patterns at different temperatures,Fe_(2)O_(3)/C molar ratios,and OC reduction degrees.Results showed that potassium hexatitanate increased carbon conversion,achieving 50%conversion at 40% potassium addition.In multi-cycle tests,carbon conversion rose with increased cycle times,reaching 84%.This improvement is attributed to ion exchange between Fe^(3+) and Ti^(4+),which induces lattice distortion and creates oxygen vacancies,enhancing OC reactivity.Potassium content remained stable during multi-cycle tests,indicating the effective potassium retention capacity of potassium hexatitanate.
基金supported by the National Natural Science Foundation of China(22478266 and 32472027)the National Key Research&Development Program of China(2022YFE0207100)the Department of Science and Technology of Sichuan Province(2024ZYD0080 and 2022YFN0027).
文摘Economical and sustainable wastewater treatment techniques are highly demanded to alleviate the issues of clearwater scarcity globally.In this work,the acetic acid/H_(2)O_(2) (AHP) was leveraged to enrich oxygenated functional groups on the biochar surface for efficient ciprofloxacin (CIP) adsorption and biochar regeneration (In situ degradation of CIP in the spent AHP solution).The AHP-modified biochar exhibited significantly enhanced CIP adsorption capacity,about 22 times that of the pristine biochar.The optimized modification condition (acetic acid/H_(2)O_(2):2.11,temperature:45 ℃,and time:12 h) was screened by the response surface method,reaching the highest CIP adsorption capacity of 86.26 mg·g^(−1).Characterization results revealed that the content of carboxyl —C=O—O was enhanced in AHP-modified biochar,which contributed to efficient CIP adsorption by the electrostatic interaction,hydrogen bonding,and hydrophobic interaction.The adsorption of modified biochar to CIP molecules was a spontaneous endothermic process,and in line with the pseudo-second-order model and the Langmuir isotherm model.Moreover,the biochar modification process enabled the spent AHP solution with a strong oxidizing agent of peracetic acid (PAA),which can be employed to degrade adsorbed CIP for biochar in-situ generation.This work tailored a closed-loop strategy for biochar oxidation,contaminant adsorption,and biochar regeneration,highlighting a viable route for sustainable wastewater treatment.
基金supported by research funds of Jeonbuk National University in 2024 and partly supported by the National Research Foundation of Korea(NRF-2019R1A2C1006441)from the Ministry of Education.
文摘Flubendiamide is a commonly used pesticide with low water solubility and a high organic carbon sorption constant,causing it to adhere to soil particles and negatively impact soil ecosystems.First,chili plant stems,typically discarded after the harvest season,represent an abundant local biomass resource with significant potential for utilization,and were converted into biochar through pyrolysis.Here,we describe the synthesis of biochar modified with iron and chitosan to increase the diversity of functions and surface functional groups of biochar.The resulting chitosan-modified magnetic biochar(CMBC)presents a full range of functional groups of chitosan and iron oxide as shown by Fourier-transform infrared spectroscopy.The correlation between flubendiamide concentration and the dose of biochar on adsorption was explored.The flubendiamide adsorption efficiency of CMBC(1%mass ratio of soil)reached 68.03%in 90 min.The highest adsorption capacity achieved was 0.95 mg·g^(−1).The flubendiamide adsorption mechanism by CMBC can be described with a pseudo-second-order kinetic model.The experiment data closely fit a Freundlich isotherm model(R^(2)=0.998),and the low residual sum of squares values demonstrate the high model applicability.In this study,we present a comprehensive overview of pesticides,alongside kinetic and isotherm model studies of flubendiamide adsorption by CMBC.We emphasize the potential of modified biochar to enhance environmental remediation applications.
基金support provided by the Center for Fabrication and Application of Electronic Materials at Dokuz Eylül University,Türkiye。
文摘Biochar and biochar composites are versatile materials that can be used in many applications.In this study,biochar was prepared from sawdust and combined with the yttrium iron garnet(YIG)nanocrystal to investigate the shielding effectiveness of the composite structure.Firstly,the effect of the pyrolysis temperature on the shielding effectiveness of biochar was investigated.Secondly,biochars combined with YIG nanocrystals with different contents and shielding effectiveness of the composites were investigated.The electromagnetic effectiveness of the samples was investigated within the X band(8-12 GHz).The findings indicate that biochar demonstrates enhanced absorption properties with elevated pyrolysis temperatures.Biochars demonstrated an approximate 40 d B shielding effectiveness,while YIG exhibited approximately 7 d B,corresponding to absorption at 8 GHz.However,the combination of biochar and YIG exhibited exceptional absorption,reaching 67.12 d B at 8 GHz.
文摘In this study,Palm kernel shell(PKS)is utilized as a raw material to produce activated biochar as adsorbent for dye removal from wastewater,specifically methylene blue(MB)dye,by utilizing a simplified and costeffective approach.Production of activated biocharwas carried out using both a furnace and a domesticmicrowave oven without an inert atmosphere.Three samples of palm kernel shell(PKS)based activated biochar labeled as samples A,B and C were carbonized inside the furnace at 800℃ for 1 h and then activated using the microwave-heating technique with varying heating times(0,5,10,and 15 min).The heating was conducted in the absence of an inert gas.Fourier Transform Infrared Spectroscopy(FTIR)highlighted a significant Si-O stretching vibration between 1040.5 to 692.7 cm−1,indicating the presence of key components(Silica and Alumina)in all PKS-based activated biochar samples.For wastewater treatment,activated biochar samples were tested against a 20 mg/LMethylene Blue(MB)solution,and the MB percentage removal was calculated for each run using a standard curve.Central Composite Design(CCD)experiments were conducted for optimization,with activated biochar Sample C exhibiting the highest adsorption capacity at 88.14%MB removal under specific conditions.ANOVA analysis confirmed the significance of the quadratic model,with a p-value of 0.0222 and R^(2)=0.9438.In conclusion,the results demonstrated the efficiency of PKS-based activated biochar as an adsorbent for MB removal in comparison to other commercial adsorbents.
基金supported by the Fundamental Research Funds for the Central Universities(No.2025JC008)the National Natural Science Foundation of China(grant number 52176105)+2 种基金the Science and Technology Project of Hebei Education Department-China(BJK2022063)the Hebei Natural Science Foundation-China(grant number E2025502038)the Funding Program for Cultivating Innovative Abilities of Graduate Students in Hebei Province of China(CXZZBS2025184).
文摘Biochar has been widely recognized as a promising solid CO_(2)adsorbent with economic and ecological benefits.Industrial CO_(2)emissions originate from diverse sources,while the pore structure and chemical functional groups of biochar exhibit varying degrees of influence on CO_(2)adsorption and separation performance under different adsorption conditions.Therefore,exploring the matching relationship between the physicochemical properties of biochar and its adsorption and separation performance at different adsorption conditions is essential for the development and optimization of carbon-based adsorbents.This study selected the high-performance extreme gradient boosting(XGB)algorithm from various algorithms and utilized it to develop CO_(2),N_(2),CH_(4)adsorption prediction models.Based on this,coupled prediction models were developed for CO_(2)/N_(2)and CO_(2)/CH_(4)adsorption selectivity.Furthermore,feature importance and partial dependence analysis were performed using SHAP values.The results indicate that during CO_(2)adsorption,the influence of the pore structure of biochar outweighs that of its chemical composition.Specifically,the pore structure of 0.4–0.6 nm is the most important property influencing CO_(2)adsorption at low and medium pressure(0–0.6 bar),and the pore structure of 0.6–0.8 nm,as well as the specific surface area contribute the most at high pressure(0.6–1 bar).During CO_(2)selective separation,the CO_(2)/N_(2)mixture is primarily separated through the selective adsorption of CO_(2)by nitrogen functional groups.In contrast,for CO_(2)/CH_(4)mixtures,pore structure<1 nm plays a more critical role in determining adsorption selectivity.In addition,molecular simulation studies further revealed the adsorption filling mechanisms of CO_(2)molecules within different pore sizes and functional groups.Finally,nitrogen-doped biochar was synthesized using de-alkalize lignin as the precursor,KOH as the activating agent,and urea as the nitrogen dopant.CO_(2),N_(2),and CH_(4)isothermal adsorption experiments were conducted,and the experimental results confirmed that the developed prediction models exhibit high accuracy(R^(2)>0.9).
基金supported by the National Natural Sci-ence Foundation of China(Nos.U21A20288 and 21978280).
文摘Developing green and efficient methods to acquire lignocellulose-based chemicals with high added value is beneficial for facilitating green chemistry and sustainable development.The goal of this study is to demonstrate that bio-based benzaldehyde,a noteworthy high-value chemical,is able to be directionally prepared from lignocellulosic biomass.This new control-lable transformation was materialized by uniting catalytic-pyrolysis of lignocellulose to toluene intermediate and catalytic oxidation of toluene intermediate to bio-based benzalde-hyde.This work also developed a highly active magnetic catalyst(CoFe_(2)O_(4)@Biochar(HTR)),achieving 77.1%benzaldehyde selectivity and 46.7%benzaldehyde yield using this catalyst.It was found that introducing the biochar carrier into the cobalt iron composite metal oxide cat-alyst enhanced hydroxyl radical formation and bio-based benzaldehyde synthesis.Based on catalyst characterizations and hydroxyl radical analysis,potential reaction mechanism for bio-based benzaldehyde synthesis was proposed.This strategy may provide a beneficial pathway for developing high-value bio-based chemical(benzaldehyde)using renewable lignocellulosic biomass.
基金Foundation item:the National Natural Science Foundation of China(20590360)the Natural Science Foundation of Shanxi Province(2006021014)+1 种基金the National Outstanding Young Scientists Foundation of China(20625620)National Key Basic Research Program of China(973 Program)(2007CB216401).
文摘A systematic study was undertaken to investigate the effects of the manganese incorporation manner on the textural properties, bulk and surface phase compositions, reduction/carburization behaviors, and surface basicity of an iron-based Fischer-Tropsch synthesis （FTS） catalyst. The catalyst samples were characterized by N2 physisorption, X-ray photoelectron spectroscopy （XPS）, H2 （or CO） temperature-programmed reduction （TPR）, CO2 temperature-programmed desorption （TPD）, and M5ssbauer spectroscopy. The FTS performance of the catalysts was studied in a slurry-phase continuously stirred tank reactor （CSTR）. The characterization results indicated that the manganese promoter incorporated by using the coprecipitation method could improve the dispersion of iron oxide, and decrease the size of the iron oxide crystallite. The manganese incorporated with the impregnation method is enriched on the catalyst＇s surface. The manganese promoter added with the impregnation method suppresses the reduction and carburization of the catalyst in H2, CO, and syngas because of the excessive enrichment of manganese on the catalyst surface. The catalyst added manganese using the coprecipitation method has the highest CO conversion （51.9%） and the lowest selectivity for heavy hydrocarbons （C12＋）.
基金the National Natural Science Foundation of China(No.22275052)the Natural Science Foundation of Hubei Province(No.2019CFB569)。
文摘Increasing environmental pollution and shortage of conventional fossil fuels have made it urgent to develop renewable and clean energy sources. Electrocatalytic water splitting, with its abundant raw materials, simple process, and zero carbon emission, is considered one of the most promising processes for producing carbon-neutral hydrogen which has excellent energy conversion efficiency and high gravimetric energy density. Among them, oxygen evolution reaction (OER) electrocatalysts and hydrogen evolution reaction (HER) electrocatalysts are critical to decreasing the intrinsic reaction energy barrier and boosting the hydrogen evolution efficiency. Therefore, it is imperative to develop and design low-cost, highly active, and stable OER and HER electrocatalysts to lower the overpotential and drive the electrocatalytic reactions. Transition metal sulfides, especially iron-based sulfides, have attracted extensive exploration by researchers as a result of its high abundance in the Earth's crust and near-metallic conductivity. Consequently, in this review, we systematically and comprehensively summarize the progress in the application of iron-based sulfides and their composites as OER and HER electrocatalysts in electrocatalysis. Detailed descriptions and illustrations of the special relationships among their composition, structure, and electrocatalytic performance are presented. Finally, this review points out the challenges and future prospects of iron-based sulfides in practical applications for designing and fabricating more promising iron-based sulfide OER and HER electrocatalysts. We believe that iron-based sulfide materials will have a wide range of application prospects as OER and HER electrocatalysts in the future.
基金supported by National Natural Science Foundation of China(Grant No.50775133)
文摘SiC magnetic abrasive is used to polish surfaces of precise,complex parts which are hard,brittle and highly corrosion-resistant in magnetic abrasive finishing(MAF).Various techniques are employed to produce this magnetic abrasive,but few can meet production demands because they are usually time-consuming,complex with high cost,and the magnetic abrasives made by these techniques have irregular shape and low bonding strength that result in low processing efficiency and shorter service life.Therefore,an attempt is made by combining gas atomization and rapid solidification to fabricate a new iron-based SiC spherical composite magnetic abrasive.The experimental system to prepare this new magnetic abrasive is constructed according to the characteristics of gas atomization and rapid solidification process and the performance requirements of magnetic abrasive.The new iron-based SiC spherical composite magnetic abrasive is prepared successfully when the machining parameters and the composition proportion of the raw materials are controlled properly.Its morphology,microstructure,phase composition are characterized by scanning electron microscope(SEM)and X-ray diffraction(XRD)analysis.The MAF tests on plate of mold steel S136 are carried out without grinding lubricant to assess the finishing performance and service life of this new SiC magnetic abrasive.The surface roughness(Ra)of the plate worked is rapidly reduced to 0.051μm from an initial value of 0.372μm within 5 min.The MAF test is carried on to find that the service life of this new SiC magnetic abrasive reaches to 155 min.The results indicate that this process presented is feasible to prepare the new SiC magnetic abrasive;and compared with previous magnetic abrasives,the new SiC spherical composite magnetic abrasive has excellent finishing performance,high processing efficiency and longer service life.The presented method to fabricate magnetic abrasive through gas atomization and rapid solidification presented can significantly improve the finishing performance and service life of magnetic abrasive,and provide a more practical approach for large-scale industrial production of magnetic abrasive.
基金supported by the National Natural Science Foundation of China (Nos. 21107125, 21577160, 51221892, 51290282 and 41201498)
文摘The heterogeneous Fenton reaction can generate highly reactive hydroxyl radicals（·OH）from reactions between recyclable solid catalysts and H2O2 at acidic or even circumneutral pH.Hence,it can effectively oxidize refractory organics in water or soils and has become a promising environmentally friendly treatment technology.Due to the complex reaction system,the mechanism behind heterogeneous Fenton reactions remains unresolved but fascinating,and is crucial for understanding Fenton chemistry and the development and application of efficient heterogeneous Fenton technologies.Iron-based materials usually possess high catalytic activity,low cost,negligible toxicity and easy recovery,and are a superior type of heterogeneous Fenton catalysts.Therefore,this article reviews the fundamental but important interfacial mechanisms of heterogeneous Fenton reactions catalyzed by iron-based materials..OH,hydroperoxyl radicals/superoxide anions（HO2./O2^-.）and high-valent iron are the three main types of reactive oxygen species（ROS）,with different oxidation reactivity and selectivity.Based on the mechanisms of ROS generation,the interfacial mechanisms of heterogeneous Fenton systems can be classified as the homogeneous Fenton mechanism induced by surface-leached iron,the heterogeneous catalysis mechanism,and the heterogeneous reaction-induced homogeneous mechanism.Different heterogeneous Fenton systems catalyzed by characteristic iron-based materials are comprehensively reviewed.Finally,related future research directions are also suggested.
基金The financial support from the National Natural Science Foundation of China (20590361)the National Outstanding Young Scientists Foundation of China (20625620)
文摘A series of iron-based Fischer-Tropsch synthesis （FTS） catalysts incorporated with Al2O3 binder were prepared by the combination of co-precipitation and spray drying technology. The catalyst samples were characterized by using N2 physical adsorption, temperature-programmed reduction/desorption （TPR/TPD） and MSssbauer effect spectroscopy （MES） methods. The characterization results indicated that the BET surface area increases with increasing Al2O3 content and passes through a maximum at the Al2O3/Fe ratio of 10/100 （weight basis）. After the point, it decreases with further increase in Al2O3 content. The incorporation of Al2O3 binder was found to weaken the surface basicity and suppress the reduction and carburization of iron-based catalysts probably due to the strong K-Al2O3 and Fe-Al2O3 interactions. Furthermore, the H2 adsorption ability of the catalysts is enhanced with increasing Al2O3 content. The FTS performances of the catalysts were tested in a slurry-phase continuously stirred tank reactor （CSTR） under the reaction conditions of 260 ℃, 1.5 MPa, 1000 h^-1 and molar ratio of H2/CO 0.67 for 200 h. The results showed that the addition of small amounts of Al2O3 affects the activity of iron-based catalysts to a little extent. However, with further increase of Al2O3 content, the FTS activity and water gas shift reaction （WGS） activity are decreased severely. The addition of appropriate Al2O3 do not affect the product selectivity, but the catalysts incorporated with large amounts of Al2O3 have higher selectivity for light hydrocarbons and lower selectivity for heavy hydrocarbons.
基金supported by National Natural Science Foundation of China(No.51374040)the National Key Scientific Instrument and Equipment Development Project of China(No.2014YQ120351)
文摘Although single-pulse lasers are often used in traditional laser-induced breakdown spectroscopy （LIBS） measurements, their measurement outcomes are generally undesirable because of the low sensitivity of carbon in iron-based alloys. In this article, a double-pulse laser was applied to improve the signal intensity of carbon. Both the inter-pulse delay and the combination of laser wavelengths in double-pulse laser-induced breakdown spectroscopy （DP-LIBS） were optimized in our experiment. At the optimized inter-pulse delay, the combination of a first laser of 532 nm and a second laser of 1,064 nm achieved the highest signal enhancement. The properties of the target also played a role in determining the mass ablation enhancement in DP-LIBS configuration.
基金supported by the National Natural Science Foundation of China(Grant Nos.90922002 and 11190023)the Fundamental Research Funds for the Central Universities of Ministry of Education of China(Grant No.2013FZA3003)
文摘The second class of high-temperature superconductors （HTSCs）, iron-based pnictides and chalcogenides, necessarily contain Fe2X2 （＂X＂ refers to a pnictogen or a chalcogen element） layers, just like the first class of HTSCs which possess the essential CuO2 sheets. So far, dozens of iron-based HTSCs, classified into nine groups, have been discovered. In this article, the crystal-chemistry aspects of the known iron-based superconductors are reviewed and summarized by employing ＂hard and soft acids and bases （HSAB）＂ concept. Based on these understandings, we propose an alternative route to exploring new iron-based superconductors via rational structural design.
基金financially supported by the National Science Fund for Excellent Young Scholars of China (No. 52022111)the Distinguished Young Scholars of China (No. 51825403)the National Natural Science Foundation of China (Nos. 51634010, 51974379)。
文摘Between the two major arsenic-containing salts in natural water, arsenite(As(Ⅲ)) is far more harmful to human and the environment than arsenate(As(V)) due to its high toxicity and transportability. Therefore, preoxidation of As(Ⅲ) to As(V) is considered to be an effective means to reduce the toxicity of arsenic and to promote the removal efficiency of arsenic. Due to their high catalytic activity and arsenic affinity, iron-based functional materials can quickly oxidize As(Ⅲ) to As(V) in heterogeneous Fenton-like systems, and then remove As(V) from water through adsorption and surface coprecipitation. In this review, the effects of different iron-based functional materials such as zero-valent iron and iron(hydroxy) oxides on arsenic removal are compared, and the catalytic oxidation mechanism of As(Ⅲ) in heterogeneous Fenton process is further clarified. Finally, the main challenges and opportunities faced by iron-based As(Ⅲ) oxidation functional materials are prospected.
