Nano-scale chemical inhomogeneity in surface oxide films formed on a V-and N-containing martensite stainless steel and tempering heating induced changes are investigated by a combination of synchrotron-based hard X-ra...Nano-scale chemical inhomogeneity in surface oxide films formed on a V-and N-containing martensite stainless steel and tempering heating induced changes are investigated by a combination of synchrotron-based hard X-ray Photoelectron emission spectroscopy(HAXPES)and microscopy(HAXPEEM)as well as microscopic X-ray absorption spectroscopy(μ-XAS)techniques.The results reveal the inhomogeneity in the oxide films on the micron-sized Cr_(2)N-and VN-type particles,while the inhomogeneity on the martensite matrix phase exists due to localised formation of nano-sized tempering nitride particles at 600℃.The oxide film formed on Cr_(2)N-type particles is rich in Cr_(2)O_(3) compared with that on the martensite matrix and VN-type particles.With the increase of tempering temperature,Cr_(2)O_(3) formation is faster for the oxidation of Cr in the martensite matrix than the oxidation of Cr nitride-rich particles.展开更多
The efficient separation of chalcopyrite(CuFeS2)and galena(PbS)is essential for optimal resource utilization.However,find-ing a selective depressant that is environmentally friendly and cost effective remains a challe...The efficient separation of chalcopyrite(CuFeS2)and galena(PbS)is essential for optimal resource utilization.However,find-ing a selective depressant that is environmentally friendly and cost effective remains a challenge.Through various techniques,such as mi-croflotation tests,Fourier transform infrared spectroscopy,scanning electron microscopy(SEM)observation,X-ray photoelectron spec-troscopy(XPS),and Raman spectroscopy measurements,this study explored the use of ferric ions(Fe^(3+))as a selective depressant for ga-lena.The results of flotation tests revealed the impressive selective inhibition capabilities of Fe^(3+)when used alone.Surface analysis showed that Fe^(3+)significantly reduced the adsorption of isopropyl ethyl thionocarbamate(IPETC)on the galena surface while having a minimal impact on chalcopyrite.Further analysis using SEM,XPS,and Raman spectra revealed that Fe^(3+)can oxidize lead sulfide to form compact lead sulfate nanoparticles on the galena surface,effectively depressing IPETC adsorption and increasing surface hydrophilicity.These findings provide a promising solution for the efficient and environmentally responsible separation of chalcopyrite and galena.展开更多
Epoxy resin-reinforced graphite composites have found extensive application as bipolar plates in fuel cells for stationary power supplies,valued for their lightweight nature and exceptional durability.To enhance the i...Epoxy resin-reinforced graphite composites have found extensive application as bipolar plates in fuel cells for stationary power supplies,valued for their lightweight nature and exceptional durability.To enhance the interfacial properties between graphite and epoxy resin(EP),surface oxidation of graphite was carried out using diverse functional groups.Experimental assessments illustrated that the composites with graphite oxide resulted in heightened mechanical strength and toughness compared to pristine graphite,which could be attributed to the excellent interface connection.Moreover,these composites displayed remarkable conductivity while simultaneously retaining their mechanical attributes.Furthermore,molecular dynamics simulations outcomes unveiled that the inclusion of oxygen-containing functional groups on the graphite surface augmented the interfacial energy with EP,and the interface morphology between graphite and resin exhibited heightened stability throughout the stretching process.This simple and effective technique presents opportunities for improving composites interfaces,enabling high load transfer efficiency,and opens up a potential path for developing strong and tough composite bipolar plates for fuel cells.展开更多
The experiment utilized commercial hot-dip Zn-1.2Al-1.2Mg(designated ZM)coated steel sheets,which were heated in a resistance furnace and held for 5 min at temperatures ranging from 600℃to 900℃.The main goal was to ...The experiment utilized commercial hot-dip Zn-1.2Al-1.2Mg(designated ZM)coated steel sheets,which were heated in a resistance furnace and held for 5 min at temperatures ranging from 600℃to 900℃.The main goal was to investigate the effect of heating temperature on the surface oxidation behavior of the ZM coating.The results show that at lower heating temperatures,the surface oxides are mainly composed of an original thin Al_(2)O_(3) layer,which acted as a barrier preventing further oxidation of the coating.By contrast,at higher heating temperatures,intermetallic phase formation caused Al_(2)O_(3) layer fragmentation.As a result,the oxide layer of the coating surface became more complex,featuring thicker Al_(2)O_(3),MgO,and ZnO.展开更多
The interaction of O2 with pyrite, marcasite and pyrrhotite surfaces was studied using first-principle calculations to obtain the oxidization mechanisms of these minerals. The results show that the adsorption energy o...The interaction of O2 with pyrite, marcasite and pyrrhotite surfaces was studied using first-principle calculations to obtain the oxidization mechanisms of these minerals. The results show that the adsorption energy of O2 on pyrrhotite surface is the largest, followed by that on marcasite surface and then pyrite surface. O2 molecules adsorbed on pyrite, marcasite and pyrrhotite surfaces are all dissociated. The oxygen atoms and surface atoms of pyrite, marcasite and pyrrhotite surfaces have different bonding structures. Due to more atoms on pyrrhotite and marcasite surfaces interaction with oxygen atoms, the adsorption energies of O2 on pyrrhotite and marcasite surfaces are larger than that on pyrite surface. Larger values of Mulliken populations for O？Fe bond of pyrrhotite surface result in relative larger adsorption energy compared with that on marcasite surface.展开更多
The effects of picosecond Nd:YAG laser irradiation on chemical and morphological surface characteristics of the commercially pure titanium and Ti–13Nb–13Zr alloy in air and argon atmospheres were studied under diffe...The effects of picosecond Nd:YAG laser irradiation on chemical and morphological surface characteristics of the commercially pure titanium and Ti–13Nb–13Zr alloy in air and argon atmospheres were studied under different laser output energy values.During the interaction of laser irradiation with the investigated materials,a part of the energy was absorbed on the target surface,influencing surface modifications.Laser beam interaction with the target surface resulted in various morphological alterations,resulting in crater formation and the presence of microcracks and hydrodynamic structures.Moreover,different chemical changes were induced on the target materials’surfaces,resulting in the titanium oxide formation in the irradiation-affected area and consequently increasing the irradiation energy absorption.Given the high energy absorption at the site of interaction,the dimensions of the surface damaged area increased.Consequently,surface roughness increased.The appearance of surface oxides also led to the increased material hardness in the surface-modified area.Observed chemical and morphological changes were pronounced after laser irradiation of the Ti–13Nb–13Zr alloy surface.展开更多
In this study, chalcopyrite was oxidized in hydrogen peroxide(H_(2)O_(2)) solutions of different concentrations to simulate different degrees of oxidation in real ores, and the effects of H_(2)O_(2) treatment on chalc...In this study, chalcopyrite was oxidized in hydrogen peroxide(H_(2)O_(2)) solutions of different concentrations to simulate different degrees of oxidation in real ores, and the effects of H_(2)O_(2) treatment on chalcopyrite surface properties and flotation performance were investigated by surface analysis techniques and floatation experiments, which implied the reason for the poor grade and recovery of oxidized chalcopyrite concentrate in the production process of the ore. Flotation results showed that when the concentration of H_(2)O_(2) increased from 0%(by weight) to 5%, the flotation recovery of chalcopyrite decreased sharply.However, with increasing H_(2)O_(2) concentration from 5% to 30%, chalcopyrite recovery improved relatively to different degrees with different collector concentrations. Analyses of X-ray photoelectron spectroscopy(XPS) and inductively coupled plasma-atomic optical emission spectrophotometry(ICP-OES) results indicated that the pretreatment with H_(2)O_(2) caused that hydrophilic substance formed on chalcopyrite surface with the dissolution of copper ions, and the dissolution amount of copper increased with the increase of H_(2)O_(2) concentration. UV–visible spectrophotometer and Fourier transform infrared spectrum(FTIR) studies indicated that the pretreatment of chalcopyrite with H_(2)O_(2) had little effect on the adsorption amount of potassium butyl xanthate(PBX) on chalcopyrite surface. However, due to the dissolution of copper ions, PBX interacted with chalcopyrite mainly as buthyl dixanthogen(BX)_(2).展开更多
The surface oxide layer of grain-oriented electrical steels was investigated by scanning electron microscopy.The formation mechanism and the influence on the glass film of the surface oxide layer were analyzed by the ...The surface oxide layer of grain-oriented electrical steels was investigated by scanning electron microscopy.The formation mechanism and the influence on the glass film of the surface oxide layer were analyzed by the calculation of thermodynamics and kinetics.The surface oxide layer with 2.3μm in thickness is mainly composed of SiO_(2),a small amount of FeO and Fe_(2)SiO_(4).During the formation of surface oxide layer,the restriction factor was the diffusion of O in the oxide layer.At the initial stage of the decarburization annealing,FeO would be formed on the surface layer.SiO_(2) and silicate particles rapidly nucleated,grew and formed a granular oxide layer in the subsurface.As the oxidation layer thickens,the nucleation of new particles decreases,and the growth of oxide particles would be dominant.A lamellar oxide layer was formed between the surface oxide layer and the steel matrix,and eventually formed a typical three-layer structure.During the high temperature annealing,MgO mainly reacted with SiO_(2) and Fe_(2)SiO_(4) in the surface oxide layer to form Mg2SiO_(4) and Fe_(2)SiO_(4) would respond first,thus forming the glass film with average thickness of 4.87μm.展开更多
Marcasite(FeS2)is widespread in nature,its oxidation plays a vital role in acid mine drainage,mineral resource recovery,and photoelectric material applications.In this paper,the oxidation mechanism of marcasite has be...Marcasite(FeS2)is widespread in nature,its oxidation plays a vital role in acid mine drainage,mineral resource recovery,and photoelectric material applications.In this paper,the oxidation mechanism of marcasite has been studied for the first time using density functional theory(DFT).It is found that,unlike the oxidation of pyrite,the oxidation of marcasite merely occurs at surface S atoms.Under the coexistence of water and oxygen,S atoms around surface Fe atoms are replaced by O atoms.The surface S sites are initially oxidized to form S==O bonds,and continue to adsorb oxygen to gradually generate SO3^2-,SO4^2-species,and eventually FeSO4.In this process,H2O molecules participate in neither oxidation nor dissociation,and they are adsorbed on surface Fe sites in the form of molecules,i.e.,all O atoms in SO4^2-derive from oxygen rather than water molecules.展开更多
The disadvantageous effects of colloidal SiO2 layer and micro-content of metal oxide adsorbed on SiC powder surface on SiC slurry stable dispersion were studied, and the novel method to avoid this disadvantage was pro...The disadvantageous effects of colloidal SiO2 layer and micro-content of metal oxide adsorbed on SiC powder surface on SiC slurry stable dispersion were studied, and the novel method to avoid this disadvantage was proposed. By acidwashing, on the one hand, because the maximum Zeta potential of SiC powder increases to 72.49 mV with the decreasing content of metal oxide adsorbed on the SiC powder surface, the repulsion force between SiC powders that dispersed in slurry is enhanced, thus the SiC powder can be fully dispersed in slurry. On the other hand, after HF acidwashing, with the OH^- group adsorbed on SiC powder surface destroyed and replaced by the Fion, the hydrogen bond adsorbed on the OHgroup is also destroyed. Therefore, the surface property of the SiC powder is changed from hydrophilic to hydrophobic; H2O that adsorbed on SiC powder surface is released and can flow freely, and it actually increases the content of the effective flow phase in the slurry. These changes of SiC powder surface property can be proved by XPS and FTIR analysis. Finally, the viscosity of SiC slurry is decreased greatly, and when the viscosity of the slurry is lower than 1 Pa·s, the solid volume fraction of SiC powder in the slurry is maximized to 61.5 vol.%.展开更多
In this study, compounded surface modification technology-high current pulsed electron beam （HCPEB） ＋ micro-plasma oxidation （MPO） was applied to treat ZK60 Mg alloys. The characteristics of the microstructure of...In this study, compounded surface modification technology-high current pulsed electron beam （HCPEB） ＋ micro-plasma oxidation （MPO） was applied to treat ZK60 Mg alloys. The characteristics of the microstructure of ZK60 Mg alloy after single MPO and HCPEB＋MPO compounded treatment were investigated by SEM. The results showed that the density of the ceramic layer of HCPEB＋MPO-treated ZK60 Mg alloy was improved and defects were reduced compared to that under MPO treatment alone. Surface modified layer of ZK60 Mg alloys treated by HCPEB＋MPO was divided into three zones, namely the top loose ceramic zone, middle compact zone and inside HCPEB-induced melted zone. Corrosion resistance of ZK60 Mg alloy before and after the compounded surface modification was measured in a solution of 3.5% NaCl by potentiodynamic polarization curves. It was found that the corrosion current density of ZK60 Mg alloys could be reduced by about three orders of magnitude, from 311μA/cm^2 of the original sample to 0.2μA/cm^2 of the HCPEB＋MPO-treated sample. This indicates the great application potential of the HCPEB＋MPO compounded surface modification technology in improving the corrosion resistance of ZK60 Mg alloys in the future.展开更多
This paper reports that the thermochromic vanadium dioxide films were deposited on various transparent substrates by radio frequency magnetron sputtering, and then aged under circumstance for years. Samples were chara...This paper reports that the thermochromic vanadium dioxide films were deposited on various transparent substrates by radio frequency magnetron sputtering, and then aged under circumstance for years. Samples were characterized with several different techniques such as x-ray diffraction, x-ray photoelectron spectroscopy, and Raman, when they were fresh from sputter chamber and aged after years, respectively, in order to determine their structure and composition. It finds that a small amount of sodium occurred on the surface of vanadium dioxide films, which was probably due to sodium ion diffusion from soda-lime glass when sputtering was performed at high substrate temperature. It also finds that aging for years significantly affected the nonstoichiometry of vanadium dioxide films, thus inducing much change in Raman modes.展开更多
The effect of surface roughness on the oxidation behavior of a directionally solidified Ni-based superalloy was investigated by surface mapping microscope,scanning electron microscope and X-ray diffraction.It was foun...The effect of surface roughness on the oxidation behavior of a directionally solidified Ni-based superalloy was investigated by surface mapping microscope,scanning electron microscope and X-ray diffraction.It was found that specimens with surface roughness of 0.05 urn exhibit the best oxidation resistance,while specimens with surface roughness of 0.14 μm behave worse than specimens with surface roughness of 0.83 μm.The specimens with surface roughness of 0.05 μm have the best oxidation resistance,which is mainly due to the smallest surface area exposed in air and thinnest work-hardening layer.The AlOlayer alleviates the oxidation process of the specimens with surface roughness of 0.83 μm,and this is the possible reason for the better oxidation resistance of samples with surface roughness of 0.83 μm than samples with surface roughness of 0.14 μm.展开更多
Constructing cerium and manganese bimetallic catalysts with excellent catalytic performance for soot combustion is the research frontier at present.In order to find out the key factors for catalytic soot combustion of...Constructing cerium and manganese bimetallic catalysts with excellent catalytic performance for soot combustion is the research frontier at present.In order to find out the key factors for catalytic soot combustion of Ce-Mn-O catalysts,a series of Ce-Mn-O catalysts with different Ce/Mn proportions were prepared by co-precipitation method.The activity test results show that it increases first and then decreases with the increase of Mn content.The best catalytic activity is obtained for Ce_(0.64)Mn_(0.36) catalyst,which shows a maximum rate temperature(T_(m)) at 306℃ for CO_(2) production in TPO curve.Compared with non-catalytic soot combustion,the T_(m) decreases by mo re than 270℃.Syste matical characte rization results suggest that when the adsorbed surface oxygen,lattice oxygen,specific surface area and total reduction amount of the catalysts reach a certain value,the key factors leading to the difference of catalytic activity become the readily reducible and highly dispersed surface manganese oxide species and contact performance of the external surface.The surface manganese oxide species is beneficial to improving the low-temperature reducibility of catalysts and the porous surface is conducive to the contact between catalyst and soot.Furthermore,for the soot combustion reaction containing only O_(2),the promoting effect of Mn^(4+)is not obvious.展开更多
Ozonation of oxalate in aqueous phase was performed with a commercial activated carbon（AC）in this work. The effect of AC dosage and solution pH on the contribution of hydroxyl radicals（HOU） in bulk solution and ox...Ozonation of oxalate in aqueous phase was performed with a commercial activated carbon（AC）in this work. The effect of AC dosage and solution pH on the contribution of hydroxyl radicals（HOU） in bulk solution and oxidation on the AC surface to the removal of oxalate was studied. We found that the removal of oxalate was reduced by tert-butyl alcohol（tBA） with low dosages of AC,while it was hardly affected by tBA when the AC dosage was greater than 0.3 g/L. tBA also inhibited ozone decomposition when the AC dosage was no more than 0.05 g/L, but it did not work when the AC dosage was no less than 0.1 g/L. These observations indicate that HOUin bulk solution and oxidation on the AC surface both contribute to the removal of oxalate. HOU oxidation in bulk solution is significant when the dosage of AC is low, whereas surface oxidation is dominant when the dosage of AC is high. The oxalate removal decreased with increasing pH of the solution with an AC dosage of 0.5 g/L. The degradation of oxalate occurs mainly through surface oxidation in acid and neutral solution, but through HOUoxidation in basic bulk solution. A mechanism involving both HOUoxidation in bulk solution and surface oxidation was proposed for AC enhanced ozonation of oxalate.展开更多
Surface oxidation of polycrystalline nickel foil in air and pure water at different temperatures and the thermal stability of the surface oxides have been investigated by means of XPS.In ad- dition to NiO,Ni_2O_3 is f...Surface oxidation of polycrystalline nickel foil in air and pure water at different temperatures and the thermal stability of the surface oxides have been investigated by means of XPS.In ad- dition to NiO,Ni_2O_3 is formed especially after long periods of air exposure.Nickel surfaces are much less reactive to pure water than to air.The thermal stability of the surface oxides is related to oxidative temperature.The surface species of oxides formed by air exposure at temperatures below 120℃ can be reduced into nickel metal after heating the sample in vacuum at 300℃ for only 10 minutes (in the case of room temperature) to 1 h (in the case of 120℃). This reduction is caused by reaction with surface carbon contaminants.However,the surface species of nickel oxides formed by air exposure with heating at temperatures above 200℃ can not be reduced into metal after heating the sample in vacuum at 300℃ for 1h.展开更多
Obtaining a detailed understanding of the surface modification of supports is crucial;however,it is a challenging task for the development and large-scale fabrication of supported electrocatalysts that can be used as ...Obtaining a detailed understanding of the surface modification of supports is crucial;however,it is a challenging task for the development and large-scale fabrication of supported electrocatalysts that can be used as alternatives to Pt-based catalysts for the oxygen reduction reaction(ORR).In this study,commercial silicon carbide(SiC)was modified through surface oxidization(O-SiC)to support the use of Pd nanoparticles(Pd NPs)as electrocatalysts for ORR.The obtained Pd/O-SiC catalysts exhibited better ORR activity,stronger durability,and higher resistance to methanol poisoning than that exhibited by commercial Pt/C.The role of the support in enhancing the ORR performance,especially the oxidization of SiC surfaces,was discussed in detail based on the experimental characterizations and density functional theory calculations.The underlying mechanism of the superior ORR performance of Pd/O-SiC catalysts was attributed to the charge transfer from SiC_(x)O_(y)to Pd NPs on the surfaces of SiC and the strong metal–support interactions(SMSIs)between Pd and SiC_(x)O_(y).The charge transfer enhanced the ORR activity by inducing electron-rich Pd,increased the adsorption of the key intermediate OOH,and decreased the Gibbs free energy of the critical ORR step.Furthermore,SMSIs enhanced the ORR stability of the Pd/O-SiC catalyst.This study provided a facile route for designing and developing highly active Pd-based ORR electrocatalysts.展开更多
By surface mechanical attrition treatment（SMAT）,a gradient nano structure（GNS） from the surface to center was generated in the AZ31 alloy sheet.The tribological behavior of AZ31 alloy with GNS was systematically i...By surface mechanical attrition treatment（SMAT）,a gradient nano structure（GNS） from the surface to center was generated in the AZ31 alloy sheet.The tribological behavior of AZ31 alloy with GNS was systematically investigated by using dry sliding tests,a 3D surface profile-meter and a scanning electron microscope equipped with an energy-dispersive spectrometer.The experimental results indicate that the Mg alloy with GNS exhibits better wear resistance comparing to the as-received sample,which is associated to the alteration of wear mechanism at different sliding speeds.The Mg alloy with GNS presents the wear mechanism of the abrasive wear at 0.05 m/s and the oxidative wear at 0.5 m/s,respectively.Moreover,the GNS can effectively promote the reaction between the oxygen and worn surface,which leads to a compact oxidation layer at 0.5 m/s.The effect of oxidation layer on the wear resistance of the Mg alloy was also discussed.展开更多
Polyacrylonitrile （PAN） based carbon fibers with different surface morphology were electrochemically treated in 3 wt% NH4HCO3 aqueous solution with current density up to 3.47 A/m 2 at room temperature, and surface s...Polyacrylonitrile （PAN） based carbon fibers with different surface morphology were electrochemically treated in 3 wt% NH4HCO3 aqueous solution with current density up to 3.47 A/m 2 at room temperature, and surface structures, surface morphology and residual mechanical properties were characterized. The crystallite size （La） of carbon fibers would be interrupted due to excessive electrochemical etching, while the crystallite spacing （d（002）） increased as increasing current density. The disordered structures on the surface of carbon fiber with rough surface increased at the initial oxidation stage and then removed by further electrochemical etching, which resulting in continuous increase of the extent of graphitization on the fiber surface. However, the electrochemical etching was beneficial to getting ordered morphology on the surface for carbon fiber with smooth surface, especially when the current density was lower than 1.77 A/m 2 . The tensile strength and tensile modulus could be improved by 17.27% and 5.75%, respectively, and was dependent of surface morphology. The decreasing density of carbon fibers probably resulted from the volume expansion of carbon fibers caused by the abundant oxygen functional groups intercalated between the adjacent graphite layers.展开更多
基金supported by the Vinnova(project number 2020-03778)supported by the Swedish Research Council(Vetenskapsradet,project number 2021-04157).
文摘Nano-scale chemical inhomogeneity in surface oxide films formed on a V-and N-containing martensite stainless steel and tempering heating induced changes are investigated by a combination of synchrotron-based hard X-ray Photoelectron emission spectroscopy(HAXPES)and microscopy(HAXPEEM)as well as microscopic X-ray absorption spectroscopy(μ-XAS)techniques.The results reveal the inhomogeneity in the oxide films on the micron-sized Cr_(2)N-and VN-type particles,while the inhomogeneity on the martensite matrix phase exists due to localised formation of nano-sized tempering nitride particles at 600℃.The oxide film formed on Cr_(2)N-type particles is rich in Cr_(2)O_(3) compared with that on the martensite matrix and VN-type particles.With the increase of tempering temperature,Cr_(2)O_(3) formation is faster for the oxidation of Cr in the martensite matrix than the oxidation of Cr nitride-rich particles.
基金the National Natural Science Foundation of China(Nos.52204298 and 52004335)the National Key R&D Program of China(Nos.2022YFC2904502 and 2022YFC2904501)+1 种基金the Major Science and Technology Projects in Yunnan Province(No.202202AB080012)the Science Research Initiation Fund of Central South University(No.202044019).
文摘The efficient separation of chalcopyrite(CuFeS2)and galena(PbS)is essential for optimal resource utilization.However,find-ing a selective depressant that is environmentally friendly and cost effective remains a challenge.Through various techniques,such as mi-croflotation tests,Fourier transform infrared spectroscopy,scanning electron microscopy(SEM)observation,X-ray photoelectron spec-troscopy(XPS),and Raman spectroscopy measurements,this study explored the use of ferric ions(Fe^(3+))as a selective depressant for ga-lena.The results of flotation tests revealed the impressive selective inhibition capabilities of Fe^(3+)when used alone.Surface analysis showed that Fe^(3+)significantly reduced the adsorption of isopropyl ethyl thionocarbamate(IPETC)on the galena surface while having a minimal impact on chalcopyrite.Further analysis using SEM,XPS,and Raman spectra revealed that Fe^(3+)can oxidize lead sulfide to form compact lead sulfate nanoparticles on the galena surface,effectively depressing IPETC adsorption and increasing surface hydrophilicity.These findings provide a promising solution for the efficient and environmentally responsible separation of chalcopyrite and galena.
基金the financial supports from the National Key R&D Program of China(No.2020YFB1505901)。
文摘Epoxy resin-reinforced graphite composites have found extensive application as bipolar plates in fuel cells for stationary power supplies,valued for their lightweight nature and exceptional durability.To enhance the interfacial properties between graphite and epoxy resin(EP),surface oxidation of graphite was carried out using diverse functional groups.Experimental assessments illustrated that the composites with graphite oxide resulted in heightened mechanical strength and toughness compared to pristine graphite,which could be attributed to the excellent interface connection.Moreover,these composites displayed remarkable conductivity while simultaneously retaining their mechanical attributes.Furthermore,molecular dynamics simulations outcomes unveiled that the inclusion of oxygen-containing functional groups on the graphite surface augmented the interfacial energy with EP,and the interface morphology between graphite and resin exhibited heightened stability throughout the stretching process.This simple and effective technique presents opportunities for improving composites interfaces,enabling high load transfer efficiency,and opens up a potential path for developing strong and tough composite bipolar plates for fuel cells.
基金financial support by the Natural Science Foundation of Shanghai(grant number 24ZR1423300).
文摘The experiment utilized commercial hot-dip Zn-1.2Al-1.2Mg(designated ZM)coated steel sheets,which were heated in a resistance furnace and held for 5 min at temperatures ranging from 600℃to 900℃.The main goal was to investigate the effect of heating temperature on the surface oxidation behavior of the ZM coating.The results show that at lower heating temperatures,the surface oxides are mainly composed of an original thin Al_(2)O_(3) layer,which acted as a barrier preventing further oxidation of the coating.By contrast,at higher heating temperatures,intermetallic phase formation caused Al_(2)O_(3) layer fragmentation.As a result,the oxide layer of the coating surface became more complex,featuring thicker Al_(2)O_(3),MgO,and ZnO.
基金Project supported by the High Level Innovation Team and Outstanding Scholar Program in Guangxi Colleges(the second batch),ChinaProjects(51304054+1 种基金51364002)supported by the National Natural Science Foundation of ChinaProject supported by the Open Foundation of Guangxi Colleges and University Key Laboratory of Minerals Engineering in Guangxi University,China
文摘The interaction of O2 with pyrite, marcasite and pyrrhotite surfaces was studied using first-principle calculations to obtain the oxidization mechanisms of these minerals. The results show that the adsorption energy of O2 on pyrrhotite surface is the largest, followed by that on marcasite surface and then pyrite surface. O2 molecules adsorbed on pyrite, marcasite and pyrrhotite surfaces are all dissociated. The oxygen atoms and surface atoms of pyrite, marcasite and pyrrhotite surfaces have different bonding structures. Due to more atoms on pyrrhotite and marcasite surfaces interaction with oxygen atoms, the adsorption energies of O2 on pyrrhotite and marcasite surfaces are larger than that on pyrite surface. Larger values of Mulliken populations for O？Fe bond of pyrrhotite surface result in relative larger adsorption energy compared with that on marcasite surface.
基金This work was financially supported by the Ministry of Education,Science and Technological Development of the Republic of Serbia through Project Nos.ON174004 and ON172019the PhD fellowship of Slađana Laketić.
文摘The effects of picosecond Nd:YAG laser irradiation on chemical and morphological surface characteristics of the commercially pure titanium and Ti–13Nb–13Zr alloy in air and argon atmospheres were studied under different laser output energy values.During the interaction of laser irradiation with the investigated materials,a part of the energy was absorbed on the target surface,influencing surface modifications.Laser beam interaction with the target surface resulted in various morphological alterations,resulting in crater formation and the presence of microcracks and hydrodynamic structures.Moreover,different chemical changes were induced on the target materials’surfaces,resulting in the titanium oxide formation in the irradiation-affected area and consequently increasing the irradiation energy absorption.Given the high energy absorption at the site of interaction,the dimensions of the surface damaged area increased.Consequently,surface roughness increased.The appearance of surface oxides also led to the increased material hardness in the surface-modified area.Observed chemical and morphological changes were pronounced after laser irradiation of the Ti–13Nb–13Zr alloy surface.
基金the support of the National Natural Science Foundation of China (No. 52174268)the Independent Exploration and Innovation Project of Graduate Students of Central South University (No. 2021zzts0885)。
文摘In this study, chalcopyrite was oxidized in hydrogen peroxide(H_(2)O_(2)) solutions of different concentrations to simulate different degrees of oxidation in real ores, and the effects of H_(2)O_(2) treatment on chalcopyrite surface properties and flotation performance were investigated by surface analysis techniques and floatation experiments, which implied the reason for the poor grade and recovery of oxidized chalcopyrite concentrate in the production process of the ore. Flotation results showed that when the concentration of H_(2)O_(2) increased from 0%(by weight) to 5%, the flotation recovery of chalcopyrite decreased sharply.However, with increasing H_(2)O_(2) concentration from 5% to 30%, chalcopyrite recovery improved relatively to different degrees with different collector concentrations. Analyses of X-ray photoelectron spectroscopy(XPS) and inductively coupled plasma-atomic optical emission spectrophotometry(ICP-OES) results indicated that the pretreatment with H_(2)O_(2) caused that hydrophilic substance formed on chalcopyrite surface with the dissolution of copper ions, and the dissolution amount of copper increased with the increase of H_(2)O_(2) concentration. UV–visible spectrophotometer and Fourier transform infrared spectrum(FTIR) studies indicated that the pretreatment of chalcopyrite with H_(2)O_(2) had little effect on the adsorption amount of potassium butyl xanthate(PBX) on chalcopyrite surface. However, due to the dissolution of copper ions, PBX interacted with chalcopyrite mainly as buthyl dixanthogen(BX)_(2).
基金Financial supports from National Key Research and Development Program(No.2016YFB0300305)National Natural Science Foundation of China(No.51804003)are gratefully acknowledged.
文摘The surface oxide layer of grain-oriented electrical steels was investigated by scanning electron microscopy.The formation mechanism and the influence on the glass film of the surface oxide layer were analyzed by the calculation of thermodynamics and kinetics.The surface oxide layer with 2.3μm in thickness is mainly composed of SiO_(2),a small amount of FeO and Fe_(2)SiO_(4).During the formation of surface oxide layer,the restriction factor was the diffusion of O in the oxide layer.At the initial stage of the decarburization annealing,FeO would be formed on the surface layer.SiO_(2) and silicate particles rapidly nucleated,grew and formed a granular oxide layer in the subsurface.As the oxidation layer thickens,the nucleation of new particles decreases,and the growth of oxide particles would be dominant.A lamellar oxide layer was formed between the surface oxide layer and the steel matrix,and eventually formed a typical three-layer structure.During the high temperature annealing,MgO mainly reacted with SiO_(2) and Fe_(2)SiO_(4) in the surface oxide layer to form Mg2SiO_(4) and Fe_(2)SiO_(4) would respond first,thus forming the glass film with average thickness of 4.87μm.
基金financial support provided by the National Natural Science Foundation of China(NSFC)(51974094,51874106,and U20A20269).
文摘Marcasite(FeS2)is widespread in nature,its oxidation plays a vital role in acid mine drainage,mineral resource recovery,and photoelectric material applications.In this paper,the oxidation mechanism of marcasite has been studied for the first time using density functional theory(DFT).It is found that,unlike the oxidation of pyrite,the oxidation of marcasite merely occurs at surface S atoms.Under the coexistence of water and oxygen,S atoms around surface Fe atoms are replaced by O atoms.The surface S sites are initially oxidized to form S==O bonds,and continue to adsorb oxygen to gradually generate SO3^2-,SO4^2-species,and eventually FeSO4.In this process,H2O molecules participate in neither oxidation nor dissociation,and they are adsorbed on surface Fe sites in the form of molecules,i.e.,all O atoms in SO4^2-derive from oxygen rather than water molecules.
基金This work was financially supported by the Doctoral Foundation of Xi'an Jiaotong University (No. DFXJTU2004-04).
文摘The disadvantageous effects of colloidal SiO2 layer and micro-content of metal oxide adsorbed on SiC powder surface on SiC slurry stable dispersion were studied, and the novel method to avoid this disadvantage was proposed. By acidwashing, on the one hand, because the maximum Zeta potential of SiC powder increases to 72.49 mV with the decreasing content of metal oxide adsorbed on the SiC powder surface, the repulsion force between SiC powders that dispersed in slurry is enhanced, thus the SiC powder can be fully dispersed in slurry. On the other hand, after HF acidwashing, with the OH^- group adsorbed on SiC powder surface destroyed and replaced by the Fion, the hydrogen bond adsorbed on the OHgroup is also destroyed. Therefore, the surface property of the SiC powder is changed from hydrophilic to hydrophobic; H2O that adsorbed on SiC powder surface is released and can flow freely, and it actually increases the content of the effective flow phase in the slurry. These changes of SiC powder surface property can be proved by XPS and FTIR analysis. Finally, the viscosity of SiC slurry is decreased greatly, and when the viscosity of the slurry is lower than 1 Pa·s, the solid volume fraction of SiC powder in the slurry is maximized to 61.5 vol.%.
基金supported by Liaoning BaiQianWan Talents Program of China (No. 2008921028)Doctoral Fund of Ministry of Education of China (No. 200801451082)
文摘In this study, compounded surface modification technology-high current pulsed electron beam （HCPEB） ＋ micro-plasma oxidation （MPO） was applied to treat ZK60 Mg alloys. The characteristics of the microstructure of ZK60 Mg alloy after single MPO and HCPEB＋MPO compounded treatment were investigated by SEM. The results showed that the density of the ceramic layer of HCPEB＋MPO-treated ZK60 Mg alloy was improved and defects were reduced compared to that under MPO treatment alone. Surface modified layer of ZK60 Mg alloys treated by HCPEB＋MPO was divided into three zones, namely the top loose ceramic zone, middle compact zone and inside HCPEB-induced melted zone. Corrosion resistance of ZK60 Mg alloy before and after the compounded surface modification was measured in a solution of 3.5% NaCl by potentiodynamic polarization curves. It was found that the corrosion current density of ZK60 Mg alloys could be reduced by about three orders of magnitude, from 311μA/cm^2 of the original sample to 0.2μA/cm^2 of the HCPEB＋MPO-treated sample. This indicates the great application potential of the HCPEB＋MPO compounded surface modification technology in improving the corrosion resistance of ZK60 Mg alloys in the future.
基金supported by the National Natural Science Foundation of China (Grant No 60776039)China Agricultural University Foundation (Grant No 2007037)
文摘This paper reports that the thermochromic vanadium dioxide films were deposited on various transparent substrates by radio frequency magnetron sputtering, and then aged under circumstance for years. Samples were characterized with several different techniques such as x-ray diffraction, x-ray photoelectron spectroscopy, and Raman, when they were fresh from sputter chamber and aged after years, respectively, in order to determine their structure and composition. It finds that a small amount of sodium occurred on the surface of vanadium dioxide films, which was probably due to sodium ion diffusion from soda-lime glass when sputtering was performed at high substrate temperature. It also finds that aging for years significantly affected the nonstoichiometry of vanadium dioxide films, thus inducing much change in Raman modes.
基金financially supported by the National Natural Science Foundation of China(No.51201164)National High Technology Research and Development Program of China(No.2012AA03A511)
文摘The effect of surface roughness on the oxidation behavior of a directionally solidified Ni-based superalloy was investigated by surface mapping microscope,scanning electron microscope and X-ray diffraction.It was found that specimens with surface roughness of 0.05 urn exhibit the best oxidation resistance,while specimens with surface roughness of 0.14 μm behave worse than specimens with surface roughness of 0.83 μm.The specimens with surface roughness of 0.05 μm have the best oxidation resistance,which is mainly due to the smallest surface area exposed in air and thinnest work-hardening layer.The AlOlayer alleviates the oxidation process of the specimens with surface roughness of 0.83 μm,and this is the possible reason for the better oxidation resistance of samples with surface roughness of 0.83 μm than samples with surface roughness of 0.14 μm.
基金Projects supported by the National Natural Science Foundation of China (21962021)Yunnan Fundamental Research Projects(202001AU070121)。
文摘Constructing cerium and manganese bimetallic catalysts with excellent catalytic performance for soot combustion is the research frontier at present.In order to find out the key factors for catalytic soot combustion of Ce-Mn-O catalysts,a series of Ce-Mn-O catalysts with different Ce/Mn proportions were prepared by co-precipitation method.The activity test results show that it increases first and then decreases with the increase of Mn content.The best catalytic activity is obtained for Ce_(0.64)Mn_(0.36) catalyst,which shows a maximum rate temperature(T_(m)) at 306℃ for CO_(2) production in TPO curve.Compared with non-catalytic soot combustion,the T_(m) decreases by mo re than 270℃.Syste matical characte rization results suggest that when the adsorbed surface oxygen,lattice oxygen,specific surface area and total reduction amount of the catalysts reach a certain value,the key factors leading to the difference of catalytic activity become the readily reducible and highly dispersed surface manganese oxide species and contact performance of the external surface.The surface manganese oxide species is beneficial to improving the low-temperature reducibility of catalysts and the porous surface is conducive to the contact between catalyst and soot.Furthermore,for the soot combustion reaction containing only O_(2),the promoting effect of Mn^(4+)is not obvious.
基金supported by the National Natural Science Foundation of China (No. 21177130)the National Key Technology R&D Program (No. 2011BAC06B09)the Chinese Academy of Sciences Visiting Professorships for Senior International Scientists (No. 2009G2-28)
文摘Ozonation of oxalate in aqueous phase was performed with a commercial activated carbon（AC）in this work. The effect of AC dosage and solution pH on the contribution of hydroxyl radicals（HOU） in bulk solution and oxidation on the AC surface to the removal of oxalate was studied. We found that the removal of oxalate was reduced by tert-butyl alcohol（tBA） with low dosages of AC,while it was hardly affected by tBA when the AC dosage was greater than 0.3 g/L. tBA also inhibited ozone decomposition when the AC dosage was no more than 0.05 g/L, but it did not work when the AC dosage was no less than 0.1 g/L. These observations indicate that HOUin bulk solution and oxidation on the AC surface both contribute to the removal of oxalate. HOU oxidation in bulk solution is significant when the dosage of AC is low, whereas surface oxidation is dominant when the dosage of AC is high. The oxalate removal decreased with increasing pH of the solution with an AC dosage of 0.5 g/L. The degradation of oxalate occurs mainly through surface oxidation in acid and neutral solution, but through HOUoxidation in basic bulk solution. A mechanism involving both HOUoxidation in bulk solution and surface oxidation was proposed for AC enhanced ozonation of oxalate.
文摘Surface oxidation of polycrystalline nickel foil in air and pure water at different temperatures and the thermal stability of the surface oxides have been investigated by means of XPS.In ad- dition to NiO,Ni_2O_3 is formed especially after long periods of air exposure.Nickel surfaces are much less reactive to pure water than to air.The thermal stability of the surface oxides is related to oxidative temperature.The surface species of oxides formed by air exposure at temperatures below 120℃ can be reduced into nickel metal after heating the sample in vacuum at 300℃ for only 10 minutes (in the case of room temperature) to 1 h (in the case of 120℃). This reduction is caused by reaction with surface carbon contaminants.However,the surface species of nickel oxides formed by air exposure with heating at temperatures above 200℃ can not be reduced into metal after heating the sample in vacuum at 300℃ for 1h.
文摘Obtaining a detailed understanding of the surface modification of supports is crucial;however,it is a challenging task for the development and large-scale fabrication of supported electrocatalysts that can be used as alternatives to Pt-based catalysts for the oxygen reduction reaction(ORR).In this study,commercial silicon carbide(SiC)was modified through surface oxidization(O-SiC)to support the use of Pd nanoparticles(Pd NPs)as electrocatalysts for ORR.The obtained Pd/O-SiC catalysts exhibited better ORR activity,stronger durability,and higher resistance to methanol poisoning than that exhibited by commercial Pt/C.The role of the support in enhancing the ORR performance,especially the oxidization of SiC surfaces,was discussed in detail based on the experimental characterizations and density functional theory calculations.The underlying mechanism of the superior ORR performance of Pd/O-SiC catalysts was attributed to the charge transfer from SiC_(x)O_(y)to Pd NPs on the surfaces of SiC and the strong metal–support interactions(SMSIs)between Pd and SiC_(x)O_(y).The charge transfer enhanced the ORR activity by inducing electron-rich Pd,increased the adsorption of the key intermediate OOH,and decreased the Gibbs free energy of the critical ORR step.Furthermore,SMSIs enhanced the ORR stability of the Pd/O-SiC catalyst.This study provided a facile route for designing and developing highly active Pd-based ORR electrocatalysts.
基金National Key Research and Development Program(No.2016YFB0701201)National Natural Science Foundation of China(Nos.51671101,51464034)+3 种基金Natural Science foundation of Jiangxi Province(No.20161ACB21003)the Scientific Research Foundation of the Education Department of Jiangxi Province(No.GJJ150010)the financial support provided by the Croucher Foundation(No.9500006)Hong Kong Collaborative Research Fund(CRF)Scheme(No.C4028-14G)
文摘By surface mechanical attrition treatment（SMAT）,a gradient nano structure（GNS） from the surface to center was generated in the AZ31 alloy sheet.The tribological behavior of AZ31 alloy with GNS was systematically investigated by using dry sliding tests,a 3D surface profile-meter and a scanning electron microscope equipped with an energy-dispersive spectrometer.The experimental results indicate that the Mg alloy with GNS exhibits better wear resistance comparing to the as-received sample,which is associated to the alteration of wear mechanism at different sliding speeds.The Mg alloy with GNS presents the wear mechanism of the abrasive wear at 0.05 m/s and the oxidative wear at 0.5 m/s,respectively.Moreover,the GNS can effectively promote the reaction between the oxygen and worn surface,which leads to a compact oxidation layer at 0.5 m/s.The effect of oxidation layer on the wear resistance of the Mg alloy was also discussed.
基金supported by the National Basic Research Program of China (No. 2011CB605602)
文摘Polyacrylonitrile （PAN） based carbon fibers with different surface morphology were electrochemically treated in 3 wt% NH4HCO3 aqueous solution with current density up to 3.47 A/m 2 at room temperature, and surface structures, surface morphology and residual mechanical properties were characterized. The crystallite size （La） of carbon fibers would be interrupted due to excessive electrochemical etching, while the crystallite spacing （d（002）） increased as increasing current density. The disordered structures on the surface of carbon fiber with rough surface increased at the initial oxidation stage and then removed by further electrochemical etching, which resulting in continuous increase of the extent of graphitization on the fiber surface. However, the electrochemical etching was beneficial to getting ordered morphology on the surface for carbon fiber with smooth surface, especially when the current density was lower than 1.77 A/m 2 . The tensile strength and tensile modulus could be improved by 17.27% and 5.75%, respectively, and was dependent of surface morphology. The decreasing density of carbon fibers probably resulted from the volume expansion of carbon fibers caused by the abundant oxygen functional groups intercalated between the adjacent graphite layers.
