To mitigate the impact of interdiffusion reactions between the silicide slurry and Ta12W alloy substrate during vacuum sintering process on the oxidation resistance of the silicide coating,a micro-arc oxidation pretre...To mitigate the impact of interdiffusion reactions between the silicide slurry and Ta12W alloy substrate during vacuum sintering process on the oxidation resistance of the silicide coating,a micro-arc oxidation pretreatment was employed to construct a Ta_(2)O_(5)ceramic layer on the Ta12W alloy surface.Subsequently,a slurry spraying-vacuum sintering method was used to prepare a Si-Cr-Ti-Zr coating on the pretreated substrate.Comparative studies were conducted on the microstructure,phase composition,and isothermal oxidation resistance(at 1600℃)of the as-prepared coatings with and without the micro-arc oxidation ceramic layer.The results show that the Ta_(2)O_(5)layer prepared at 400 V is more continuous and has smaller pores than that prepared at 350 V.After microarc oxidation pretreatment,the Si-Cr-Ti-Zr coating on Ta12W alloy consists of three distinct layers:an upper layer dominated by Ti_(5)Si_(3),Ta_(5)Si_(3),and ZrSi;a middle layer dominated by TaSi_(2);a coating/substrate interfacial reaction layer dominated by Ta_(5)Si_(3).Both the Si-Cr-Ti-Zr coatings with and without the Ta_(2)O_(5)ceramic layer do not fail after isothermal oxidation at 1600℃for 5 h.Notably,the addition of the Ta2O5 ceramic layer reduces the high-temperature oxidation rate of the coating.展开更多
In this work,we constructed a three-dimensional electrochemical system(3D-ECO),which included the cathode and anode electrode plates,as well as the screening of three-dimensional particle electrodes and parameter opti...In this work,we constructed a three-dimensional electrochemical system(3D-ECO),which included the cathode and anode electrode plates,as well as the screening of three-dimensional particle electrodes and parameter opti-mization,for the degradation of landfill leachate(LL)containing elevated levels of tetracycline(TC),and explored its mechanism of action.Firstly,titanium-based ruthenium-iridium(Ti/RuO_(2)-IrO_(2)),titanium-based ruthenium-iridium-platinum(Ti/Pt-RuO_(2)-IrO_(2)),and titanium-based tin-antimony(Ti/SnO_(2)-Sb_(2)O_(3))were employed as an-odes in the electrocatalytic oxidation system,with titanium and stainless steel plates serving as cathodes,to construct the optimal two-dimensional electrocatalytic oxidation system(2D-ECO)through cross-comparison ex-periments.Subsequently,using granular activated carbon(GAC),coconut shell biochar(CBC),walnut shell carbon(WBC),and bamboo charcoal(BBC)as particle electrodes,a 3D-ECO system was developed.The influence of var-ious operational parameters on treating TC-containing LL was investigated.The optimal operating parameters obtained from the study was:pH=5,current density of 30 mA/cm^(2),particle dosage of 7 g/L,particle size ranging from 1.70 to 2.00 mm,and electrode spacing of 4 cm.Under these conditions,the COD removal rate of 3D-ECO within three hours was 90.25%,the TC removal rate was 72.41%,and the NH_(3)-N removal rate was 39.52%.The removal of TC followed a pseudo-first-order kinetic model.Additionally,degradation mechanisms were elucidated through electron paramagnetic resonance(EPR)spectrometer and Tert-Butanol(TBA)quenching experiments,indicating that the degradation primarily occurred through a non-radical(1O_(2))pathway.This re-search offers a comprehensive analysis of the simultaneous breakdown of intricate LL matrices and TC,enhancing our comprehension of the degradation processes and underlying mechanisms.展开更多
TiB_(2)coatings can significantly enhance the high-temperature oxidation resistance of molybdenum,which would broaden the application range of molybdenum and alloys thereof.However,traditional methods for preparing Ti...TiB_(2)coatings can significantly enhance the high-temperature oxidation resistance of molybdenum,which would broaden the application range of molybdenum and alloys thereof.However,traditional methods for preparing TiB_(2)coatings have disadvantages such as high equipment costs,complicated processes,and highly toxic gas emissions.This paper proposes an environmentally friendly method,which requires inexpensive equipment and simple processing,for preparing TiB_(2)coating on molybdenum via electrophoretic deposition within Na3AlF6-based molten salts.The produced TiB_(2)layer had an approximate thickness of 60μm and exhibited high density,outstanding hardness(38.2 GPa)and robust adhesion strength(51 N).Additionally,high-temperature oxidation experiments revealed that,at900℃,the TiB_(2)coating provided effective protection to the molybdenum substrate against oxidation for 3 h.This result indicates that the TiB_(2)coating prepared on molybdenum using molten salt electrophoretic deposition possesses good high-temperature oxidation resistance.展开更多
Co-based alloy coating was prepared on Zr alloy using laser melting and cladding technique to study the difference in the high-temperature oxidation behavior between pure metal Co coatings and Co-T800 alloy coatings,a...Co-based alloy coating was prepared on Zr alloy using laser melting and cladding technique to study the difference in the high-temperature oxidation behavior between pure metal Co coatings and Co-T800 alloy coatings,as well as the wear resistance of the coatings.Besides,the effect of changing the laser melting process on the coatings was also investigated.The oxidation mass gain at 800–1200℃and the high-temperature oxidation behavior during high-temperature treatment for 1 h of two coated Zr alloy samples were studied.Results show that the Co coating and the Co-T800 coating have better resistance against high-temperature oxidation.After oxidizing at 1000℃for 1 h,the thickness of the oxide layer of the uncoated sample was 241.0μm,whereas that of the sample with Co-based coating is only 11.8–35.5μm.The friction wear test shows that the depth of the abrasion mark of the coated sample is only 1/2 of that of the substrate,indicating that the hardness and wear resistance of the Zr substrate are greatly improved.The disadvantage of Co-based coatings is the inferior corrosion resistance in 3.5wt%NaCl solution.展开更多
Powder metallurgy was used to fabricate TiC-NiCr cermets and the oxidation behavior at 900℃ was investigated.Results reveal that TiC-NiCr cermets have uniform structures with excellent mechanical properties,whose har...Powder metallurgy was used to fabricate TiC-NiCr cermets and the oxidation behavior at 900℃ was investigated.Results reveal that TiC-NiCr cermets have uniform structures with excellent mechanical properties,whose hardness is 65 HRC and flexural strength is 1450 MPa.The high-temperature oxidation mechanism of TiC-based cermets was investigated through an X-ray diffractometer and scanning electron microscope.The added elements Ni and Cr along with their solid solutions not only bond with the hard phase TiC to ensure the physical performance of the cermet,but also impede the internal diffusion during oxidation by forming a dense composite oxide layer,thereby enhancing the oxidation resistance.The TiC-NiCr cermet exhibits a dense protective oxide layer at 900℃ and can endure continuous oxidation for approximately 1000 h.A methodology for fabricating TiC-NiCr metal matrix composites is proposed,and their oxidation resistance is evaluated,providing a theoretical and practical basis for simultaneously enhancing the mechanical properties and oxidation resistance and reducing production costs.展开更多
To improve the high-temperature oxidation resistance of TiAlNb9 alloy,a Cr-Al-Y co-deposition coating was prepared on the alloy surface by the pack cementation method.The microstructure of the coating was analyzed by ...To improve the high-temperature oxidation resistance of TiAlNb9 alloy,a Cr-Al-Y co-deposition coating was prepared on the alloy surface by the pack cementation method.The microstructure of the coating was analyzed by scanning electron microscope,energy dispersive spectrometer,and X-ray diffractometer,and the high-temperature oxidation properties of the substrate and coating at 1273 K were compared and studied.The results show that the Cr-Al-Y coating is about 30μm in thickness,and it has a dense structure and good film-substrate bonding.The coating includes an outer layer composed of TiCr_(2),TiCr,Ti_(4)Cr,and(Ti,Nb)Cr_(4) phases as well as an inner layer composed of Ti_(2)Al,and Nb-richγ-TiAl interdiffusion zone.The TiAlNb9 substrate forms an oxide layer composed of TiO_(2) and Al_(2)O_(3) at 1273 K.Due to its loose and porous structure,TiO_(2) oxide film cannot effectively isolate the internal diffusion of element O,resulting in continuous oxidation damage to the substrate.The Cr-Al-Y co-deposition coating forms a dense Cr_(2)O_(3) and Al_(2)O_(3) oxide layer during oxidation,effectively preventing the internal diffusion of element O and significantly improving the high-temperature oxidation resistance of the substrate alloy.展开更多
The high-temperature oxidation resistance of AISI 321 stainless steel used in solar thermal power heat exchangers determines its service life.In this study,aluminizing and subsequent laser shock peening(LSP)treatments...The high-temperature oxidation resistance of AISI 321 stainless steel used in solar thermal power heat exchangers determines its service life.In this study,aluminizing and subsequent laser shock peening(LSP)treatments were employed to improve the high-temperature oxidation resistance of AISI 321 stainless steel at 620°C.These two treatments decreased the oxidation rate of AISI 321 steel.Specifically,the optimal oxidation resistance was observed in aluminized steel before oxidation for 144 h owing to the increased entropy of the LSP-treated specimen.After 144 h,LSP-treated steel achieved the best oxidation resistance because of the formation of a protectiveα-Al2O3film.Moreover,the large amount of subgrain boundaries formed on the aluminized layer of the LSP-treated samples could act as short-circuit paths for the outward diffusion of Al,facilitating the rapid nucleation ofα-Al2O3.Meanwhile,the aluminized layer could isolate the contact between the oxidation environment and matrix,thereby decreasing the oxidation rate.Furthermore,the minimum oxidation parabolic constant was calculated for LSP-treated steel(6.45787×10^(-14)),which was 69.18%and 36.36%that of aluminized and 321 steel,respectively,during the entire oxidation process.Therefore,the combination of aluminizing and LSP treatments can improve the high-temperature oxidation resistance of 321 stainless steel,providing a new idea for its surface treatment to achieve a long service life at high temperatures.展开更多
Enhancing the activity of photocatalysts is a critical challenge for improving the photocatalytic degradation of contaminated wastewater.Here,a novel Ce single-atom-doped titanate nanotube photocatalyst(CeH_(2)Ti_(2)O...Enhancing the activity of photocatalysts is a critical challenge for improving the photocatalytic degradation of contaminated wastewater.Here,a novel Ce single-atom-doped titanate nanotube photocatalyst(CeH_(2)Ti_(2)O_(5)·H_(2)O)was successfully synthesized using a onepot solvothermal method.Degradation experiments revealed that the optimal Ce doping ratio was 1.0%.The ultraviolet-visible diffuse reflectance spectroscopy results showed that the bandgap of the Ce-doped sample decreased from 3.02 to 2.87 eV,enhancing the absorption in the visible spectral range.At the same time,the BrunauerEmmett-Teller specific surface area increased from 63.68 to 88.95 m^(2)g^(-1).The 1.0%Ce-H_(2)Ti_(2)O_(5)·H_(2)O(HTC_(1))could degrade 99.04%of 100 mg L-1rhodamine B(RhB)after 40 min of visible-light irradiation.The degradation efficiency decreased by only 21.24%after five cycles.The results of free-radical quenching and electron spin resonance spectroscopy analyses indicated that HTC_(1)achieved efficient degradation of RhB through a direct hole oxidation mechanism.Compared with pure protonated titanate nanotubes(H_(2)Ti_(2)O_(5)·H_(2)O),HTC_(1)had a higher specific surface area,more electron traps,narrower bandgap,longer hole lifetime,and suppressed photogenerated charge recombination rate owing to the Ce single-atom doping.展开更多
The large molecular weight and high hydrophilicity of chloramphenicol(CAP) residuals in wastewater led to severe degradation difficulty,which propelled the development of new wastewater degradation processes and react...The large molecular weight and high hydrophilicity of chloramphenicol(CAP) residuals in wastewater led to severe degradation difficulty,which propelled the development of new wastewater degradation processes and reactors based on process intensification.This study enhanced the CAP degradation by ozone/peroxydisulfate(PDS) advanced oxidation process in a submerged rotating packed bed(SRPB)reactor.Compared the usage of different oxidants,it was indicated that the combination of O_(3) and PDS exhibited a higher degradation efficiency than ozone and PDS alone.The more desired degradation efficiency could be achieved at the operating conditions of ascending PDS concentration,SRPB rotational speed,ozone concentration,reduced initial CAP concentration,and the water qualities of ascended pH,lower Cl^(-)and initial CO_(3)^(2-) concentrations.Under the optimized conditions of C_(CAP)=20 mg·L^(-1),C_(O3)=30 mg·L^(-1),C_(PDS)=100 mg·L^(-1),and N=400 r·min^(-1),and water qualities of pH=10,the maximum chloramphenicol degradation efficiency of 97% and kinetic constant of 0.23 min^(-1) were achieved after treating 16 min.A comparison of the results with previously reported advanced oxidation processes of CAP indicated that the enhanced O^(3)/PDS advanced oxidation system using the SRPB can significantly improve the degradation efficiency of CAP.展开更多
To improve the high-temperature service properties of coppery tuyere,Co06 coating with a Ni60A interlayer was prepared on copper by plasma cladding.Ni60A interlayer acted as a bridge to promote the element diffusion,t...To improve the high-temperature service properties of coppery tuyere,Co06 coating with a Ni60A interlayer was prepared on copper by plasma cladding.Ni60A interlayer acted as a bridge to promote the element diffusion,thus achieving metallurgical bonding.Due to the strengthening effect ofγ-Co,Cr_(23)C_(6)and Cr_(7)C_(3)phases,the wear resistance of Co06–Ni60A coating was much higher than that of copper substrate.As the temperature increased,the wear resistance of coating decreased first and then increased.The coating exhibited better wear resistance at 600℃ due to the oxidation wear mechanism.Compared with copper substrate and Ni60A,the oxidation resistance of Co06 was increased by 6.0 and 1.9 times,respectively.For melting loss resistance,Co06–Ni60A coating was superior to Ni60A single-layer coating,but the molten iron can still form a micro-metallurgical bonding with the coating surface.展开更多
Addressing the growing challenge of water contamination,this study comparatively evaluated a persulfate(PDS)system activated by nonradical nitrogen-doped carbon nanotubes(N-CNTs)versus a PDS system activated by radica...Addressing the growing challenge of water contamination,this study comparatively evaluated a persulfate(PDS)system activated by nonradical nitrogen-doped carbon nanotubes(N-CNTs)versus a PDS system activated by radical-based iron(Fe^(2+)),both used for the degradation of bisphenol A(BPA).The N-CNTs/PDS system,driven by the electron transfer mechanism,achieved remarkable 90.9%BPA removal within 30 min at high BPA concentrations,significantly outperforming the Fe^(2+)/PDS system,which attained only 38.9%removal.The N-CNTs/PDS system maintained robust degradation efficiency across a wide range of BPA concentrations and exhibited a high degree of resilience in diverse water matrices.By directly abstracting electrons from BPA molecules,the N-CNTs/PDS system effectively minimised oxidant wastage and mitigated the risk of secondary pollution,ensuring efficient utilisation of active sites on N-CNTs and sustaining a high catalytic rate.The formation of the N-CNTs-PDS^(*)complex significantly enhanced BPA degradation and mineralisation,thereby optimising PDS consumption.These findings highlight the unparalleled advantages of the N-CNTs/PDS system in managing complex wastewater,offering a promising and innovative solution for treating complex industrial wastewater and advancing environmental remediation efforts.展开更多
Ni-La2O3/CeO2 composite films were prepared by electrodeposition from a nickel sulfate bath containing certain content of micrometer and nanometer La2O3/CeO2 particles. The effect of La2O3 or CeO2 particle size on the...Ni-La2O3/CeO2 composite films were prepared by electrodeposition from a nickel sulfate bath containing certain content of micrometer and nanometer La2O3/CeO2 particles. The effect of La2O3 or CeO2 particle size on the oxidation resistance of the electrodeposited Ni-La2O3/CeO2 composites in air at 1000 °C was studied. The results indicate that, compared with the electrodeposited Ni-film, Ni-La2O3/CeO2 composites exhibit a superior oxidation resistance due to the codeposited La2O3 or CeO2 particles blocking the outward diffusion of nickel. Moreover, compared with nanoparticles, La2O3 or CeO2 microparticles have stronger effect because La2O3 or CeO2 microparticles also act as a diffusion barrier layer at the onset of oxidation.展开更多
Manganese oxides are known as one type of semiconductors,but their photocatalysis characteristics have not been deeply explored.In this study,photocatalytic degradation of phenol using several synthesized manganese ox...Manganese oxides are known as one type of semiconductors,but their photocatalysis characteristics have not been deeply explored.In this study,photocatalytic degradation of phenol using several synthesized manganese oxides,i.e,acidic birnessite （BIR-H）,alkaline birnessite （BIR-OH）,cryptomelane （CRY） and todorokite （TOD）,were comparatively investigated.To elucidate phenol degradation mechanisms,X-ray diffraction （XRD）,ICP-AES （inductively coupled plasma-atomic emission spectroscopy）,TEM （transmission electronic microscope）,N 2 physisorption at 77 K and UV-visible diffuse reflectance spectroscopy （UV-Vis DRS） were employed to characterize the structural,compositional,morphological,specific surface area and optical absorption properties of the manganese oxides.After 12 hr of UV-Vis irradiation,the total organic carbon （TOC） removal rate reached 62.1%,43.1%,25.4%,and 22.5% for cryptomelane,acidic birnessite,todorokite and alkaline birnessite,respectively.Compared to the reactions in the dark condition,UV- Vis exposure improved the TOC removal rates by 55.8%,31.9%,23.4% and 17.9%.This suggests a weak ability of manganese oxides to degrade phenol in the dark condition,while UV-Vis light irradiation could significantly enhance phenol degradation.The manganese minerals exhibited photocatalytic activities in the order of：CRY BIR-H TOD BIR-OH.There may be three possible mechanisms for photochemical degradation：（1） direct photolysis of phenol;（2） direct oxidation of phenol by manganese oxides;（3） photocatalytic oxidation of phenol by manganese oxides.Photocatalytic oxidation of phenol appeared to be the dominant mechanism.展开更多
The 2,4,6-trinitrotoluene （TNT） is a potential carcinogens and TNT contaminated wastewater, which could not be effectively disposed with conventional treatments. The supercritical water oxidation （SCWO） to treat T...The 2,4,6-trinitrotoluene （TNT） is a potential carcinogens and TNT contaminated wastewater, which could not be effectively disposed with conventional treatments. The supercritical water oxidation （SCWO） to treat TNT contaminated wastewater was studied in this article, The TNT concentration in wastewater was measured by high-performance liquid chromatograph （HPLC） and the degraded intermediates were analyzed using GC-MS. The results showed that SCWO could degrade TNT efficiently in the presence of oxygen. The reaction temperature, pressure, residence time and oxygen excess were the main contributing factors in the process. The decomposition of TNT was accelerated as the temperature or residence time increased. At 550℃, 24 MPa, 120 s and oxygen excess 300%, TNT removal rate could exceed 99.9%. Partial oxidation occured in SCWO without oxygen. It was concluded that supercritical water was a good solvent and had excellent oxidation capability in the existence of oxygen. The main intermediates of TNT during SCWO included toluene, 1,3,5-trinitrobenzene, nitrophenol, naphthalene, fluorenone, dibutyl phthalate, alkanes and several dimers based on the intermediate analysis. Some side reactions, such as coupled reaction, hydrolysis reaction and isomerization reaction may take place simultaneously when TNT was oxidized by SCWO.展开更多
A novel process, microwave assisted catalytic wet air oxidation(MW-CWO), was applied for the degradation of H-acid(1-amino-8-naphthol-3, 6-disulfonic acid) in aqueous solution. Ni-loaded granular activated carbon(GAC)...A novel process, microwave assisted catalytic wet air oxidation(MW-CWO), was applied for the degradation of H-acid(1-amino-8-naphthol-3, 6-disulfonic acid) in aqueous solution. Ni-loaded granular activated carbon(GAC), prepared by immersion-calcination method, was used as catalyst. The results showed that the MW-CWO process was very effective for the degradation of H-acid in aqueous solution under atmospheric pressure with 87.4% TOC (total organic carbon) reduction in 20 min. Ni on GAC existed in the form of NiO as specified by XRD. Loss of Ni was significant in the initial stage, and then remained almost constant after 20 min reaction. BET surface area results showed that the surface property of GAC after MW-CWO process was superior to that of blank GAC.展开更多
The degradation capacity of advanced oxidants generated from oxygen reduction was investigated in model effluent containing chlorobenzene, aniline and benzene through the advanced oxidation processes(AOPs). Intermedia...The degradation capacity of advanced oxidants generated from oxygen reduction was investigated in model effluent containing chlorobenzene, aniline and benzene through the advanced oxidation processes(AOPs). Intermediate products of the degradation process were determined by GC–MS, and they contributed to specify the degradation pathways of monoaromatic compounds. The study particularly focused on the influence of the dosage of the oxidant, pH and the initial concentration of organic compounds on the degradation effectiveness.When the dosage of oxidant was 4 wt% and the pH was 7, the maximum degradation rates of 74.83% chlorobenzene, 70.32% aniline and 37.69% benzene were achieved. Furthermore, microwave was applied to intensify the oxidation process under optimal operation conditions, and the degradation rates were increased to 87.85% chlorobenzene, 89.11% aniline and 39.03% benzene, respectively.展开更多
The oxidation behavior and mechanism of as-received and 30 % cold-rolled alumina-forming austenitic(AFA) steel were investigated in dry air at 700℃.The results show that the mass gain per unit area curves of as-recei...The oxidation behavior and mechanism of as-received and 30 % cold-rolled alumina-forming austenitic(AFA) steel were investigated in dry air at 700℃.The results show that the mass gain per unit area curves of as-received and 30 % cold-rolled steels subject to near-parabolic law before 100 h oxidation time.Two samples both show higher high-temperature oxidation resistance due to the formation of dense Al_(2)O_(3) oxide scale.Gradual spallation of outer scale results in the formation of continuous and dense alumina scale.Dislocations can act as short-circuit diffusion channel for the diffusion of Al from alloy matrix to surface,and also provide nucleation sites for B2-NiAl phase,which ensure the continuous formation of Al_(2)O_(3) scale.展开更多
High-temperature oxidation is a common failure in high-temperature environments,which widely occur in aircraft engines and aerospace thrusters;as a result,the development of anti-high-temperature oxidation materials h...High-temperature oxidation is a common failure in high-temperature environments,which widely occur in aircraft engines and aerospace thrusters;as a result,the development of anti-high-temperature oxidation materials has been pursued.Ni-based alloys are a common high-temperature material;however,they are too expensive.High-entropy alloys are alternatives for the anti-oxidation property at high temperatures because of their special structure and properties.The recent achievements of high-temperature oxidation are reviewed in this paper.The high-temperature oxidation environment,temperature,phase structure,alloy elements,and preparation methods of high-entropy alloys are summarized.The reason why high-entropy alloys have anti-oxidation ability at high temperatures is illuminated.Current research,material selection,and application prospects of high-temperature oxidation are introduced.展开更多
Herein,we prepa red novel three-dimensional(3D)gear-s haped Co3O4@C(Co3O4 modified by amorphous carbon)and sheet-like SnO2/CC(SnO2 grow on the carbon cloth)as anode and cathode to achieve efficient removal of 4-nitrop...Herein,we prepa red novel three-dimensional(3D)gear-s haped Co3O4@C(Co3O4 modified by amorphous carbon)and sheet-like SnO2/CC(SnO2 grow on the carbon cloth)as anode and cathode to achieve efficient removal of 4-nitrophenol(4-NP)in the presence of peroxymonosulfate(PMS)and simultaneous electrocatalytic reduction of CO2,respectively.In this process,4-NP was mineralized into CO2 by the Co3O4@C,and the generated CO2 was reduced into HCOOH by the sheet-like SnO2/CC cathode.Compared with the pure Co0.5(Co3O4 was prepared using 0.5 g urea)with PMS(30 mg,0.5 g/L),the degradation efficiency of 4-NP(60 mL,10 mg/L)increased from 74.5%-85.1%in 60 min using the Co0.5 modified by amorphous carbon(Co0.5@C).Furthermore,when the voltage of 1.0 V was added in the anodic system of Co0.5@C with PMS(30 mg,0.5 g/L),the degradation efficiency of 4-NP increased from 85.1%-99.1%when Pt was used as cathode.In the experiments of 4-NP degradation coupled with simultaneous electrocatalytic CO2 reduction,the degradation efficiency of 4-NP was 99.0%in the anodic system of Co0.5@C with addition of PMS(30 mg,0.5 g/L),while the Faraday efficiency(FE)of HCOOH was 24.1%at voltage of-1.3 V using the SnO2/CC as cathode.The results showed that the anode of Co3O4 modified by amorphous carbon can markedly improve the degradation efficiency of 4-NP,while the cathode of SnO2/CC can greatly improve the FE and selectivity of CO2 reduction to HCOOH and the stability of cathode.Finally,the promotion mechanism was proposed to explain the degradation of organic pollutants and reduction of CO2 into HCOOH in the process of electrocatalysis coupled with advanced oxidation processes(AOPs)and simultaneous CO2 reduction.展开更多
The kinetic curve of the high-temperature oxidation of austenitie stainless steel Crl8Ni11 Cu3Al3MnNb at different temperatures was measured by weighting method. It is showed that the oxidation curves at 700 and 800 ...The kinetic curve of the high-temperature oxidation of austenitie stainless steel Crl8Ni11 Cu3Al3MnNb at different temperatures was measured by weighting method. It is showed that the oxidation curves at 700 and 800 ℃ followed the parabolic law, and the steel presented an excellent anti-oxidation. The surface morphology and structure of the oxide film were studied by scanning electron microscopy and X-ray diffraction methods. A dense oxide film was attained at 700 and 800 ℃, mainly composed of the hexagonal Al2 O3, Fe2 O3, and a small amount oxide of Cr at 700 ℃. At 900 ℃ the oxide film started to delaminate, and was composed of （Cr,Fe）2O3 and the spinel CuCrMnO4 and Fe（Cr, Al） 2O3.展开更多
基金National Natural Science Foundation of China(52071274)Key Research and Development Projects of Shaanxi Province(2023-YBGY-442)Science and Technology Nova Project-Innovative Talent Promotion Program of Shaanxi Province(2020KJXX-062)。
文摘To mitigate the impact of interdiffusion reactions between the silicide slurry and Ta12W alloy substrate during vacuum sintering process on the oxidation resistance of the silicide coating,a micro-arc oxidation pretreatment was employed to construct a Ta_(2)O_(5)ceramic layer on the Ta12W alloy surface.Subsequently,a slurry spraying-vacuum sintering method was used to prepare a Si-Cr-Ti-Zr coating on the pretreated substrate.Comparative studies were conducted on the microstructure,phase composition,and isothermal oxidation resistance(at 1600℃)of the as-prepared coatings with and without the micro-arc oxidation ceramic layer.The results show that the Ta_(2)O_(5)layer prepared at 400 V is more continuous and has smaller pores than that prepared at 350 V.After microarc oxidation pretreatment,the Si-Cr-Ti-Zr coating on Ta12W alloy consists of three distinct layers:an upper layer dominated by Ti_(5)Si_(3),Ta_(5)Si_(3),and ZrSi;a middle layer dominated by TaSi_(2);a coating/substrate interfacial reaction layer dominated by Ta_(5)Si_(3).Both the Si-Cr-Ti-Zr coatings with and without the Ta_(2)O_(5)ceramic layer do not fail after isothermal oxidation at 1600℃for 5 h.Notably,the addition of the Ta2O5 ceramic layer reduces the high-temperature oxidation rate of the coating.
基金supported by the National Natural Science Foundation of China(Nos.42477406 and 51878617)the Horizontal Scientific Research Project(No.KYY-HX-20220803)the Engineering Research Center of Ministry of Education for Renewable Energy Infrastructure Construction Technology.
文摘In this work,we constructed a three-dimensional electrochemical system(3D-ECO),which included the cathode and anode electrode plates,as well as the screening of three-dimensional particle electrodes and parameter opti-mization,for the degradation of landfill leachate(LL)containing elevated levels of tetracycline(TC),and explored its mechanism of action.Firstly,titanium-based ruthenium-iridium(Ti/RuO_(2)-IrO_(2)),titanium-based ruthenium-iridium-platinum(Ti/Pt-RuO_(2)-IrO_(2)),and titanium-based tin-antimony(Ti/SnO_(2)-Sb_(2)O_(3))were employed as an-odes in the electrocatalytic oxidation system,with titanium and stainless steel plates serving as cathodes,to construct the optimal two-dimensional electrocatalytic oxidation system(2D-ECO)through cross-comparison ex-periments.Subsequently,using granular activated carbon(GAC),coconut shell biochar(CBC),walnut shell carbon(WBC),and bamboo charcoal(BBC)as particle electrodes,a 3D-ECO system was developed.The influence of var-ious operational parameters on treating TC-containing LL was investigated.The optimal operating parameters obtained from the study was:pH=5,current density of 30 mA/cm^(2),particle dosage of 7 g/L,particle size ranging from 1.70 to 2.00 mm,and electrode spacing of 4 cm.Under these conditions,the COD removal rate of 3D-ECO within three hours was 90.25%,the TC removal rate was 72.41%,and the NH_(3)-N removal rate was 39.52%.The removal of TC followed a pseudo-first-order kinetic model.Additionally,degradation mechanisms were elucidated through electron paramagnetic resonance(EPR)spectrometer and Tert-Butanol(TBA)quenching experiments,indicating that the degradation primarily occurred through a non-radical(1O_(2))pathway.This re-search offers a comprehensive analysis of the simultaneous breakdown of intricate LL matrices and TC,enhancing our comprehension of the degradation processes and underlying mechanisms.
基金supported by the Original Exploratory Program of the National Natural Science Foundation of China(No.52450012)。
文摘TiB_(2)coatings can significantly enhance the high-temperature oxidation resistance of molybdenum,which would broaden the application range of molybdenum and alloys thereof.However,traditional methods for preparing TiB_(2)coatings have disadvantages such as high equipment costs,complicated processes,and highly toxic gas emissions.This paper proposes an environmentally friendly method,which requires inexpensive equipment and simple processing,for preparing TiB_(2)coating on molybdenum via electrophoretic deposition within Na3AlF6-based molten salts.The produced TiB_(2)layer had an approximate thickness of 60μm and exhibited high density,outstanding hardness(38.2 GPa)and robust adhesion strength(51 N).Additionally,high-temperature oxidation experiments revealed that,at900℃,the TiB_(2)coating provided effective protection to the molybdenum substrate against oxidation for 3 h.This result indicates that the TiB_(2)coating prepared on molybdenum using molten salt electrophoretic deposition possesses good high-temperature oxidation resistance.
基金National Natural Science Foundation of China(52071126)Natural Science Foundation of Tianjin City,China(22JCQNJC01240)+2 种基金Central Guidance on Local Science and Technology Development Fund of Hebei Province(226Z1009G)Special Funds for Science and Technology Innovation in Hebei(2022X19)Anhui Provincial Natural Science Foundation(2308085ME135)。
文摘Co-based alloy coating was prepared on Zr alloy using laser melting and cladding technique to study the difference in the high-temperature oxidation behavior between pure metal Co coatings and Co-T800 alloy coatings,as well as the wear resistance of the coatings.Besides,the effect of changing the laser melting process on the coatings was also investigated.The oxidation mass gain at 800–1200℃and the high-temperature oxidation behavior during high-temperature treatment for 1 h of two coated Zr alloy samples were studied.Results show that the Co coating and the Co-T800 coating have better resistance against high-temperature oxidation.After oxidizing at 1000℃for 1 h,the thickness of the oxide layer of the uncoated sample was 241.0μm,whereas that of the sample with Co-based coating is only 11.8–35.5μm.The friction wear test shows that the depth of the abrasion mark of the coated sample is only 1/2 of that of the substrate,indicating that the hardness and wear resistance of the Zr substrate are greatly improved.The disadvantage of Co-based coatings is the inferior corrosion resistance in 3.5wt%NaCl solution.
基金National Natural Science Foundation of China(52376076)Open Fund of Material Corrosion and Protection Key Laboratory of Sichuan Province(2023CL13)Laiwu Vocational and Technical College Teachers Research Fund(2023jsky05)。
文摘Powder metallurgy was used to fabricate TiC-NiCr cermets and the oxidation behavior at 900℃ was investigated.Results reveal that TiC-NiCr cermets have uniform structures with excellent mechanical properties,whose hardness is 65 HRC and flexural strength is 1450 MPa.The high-temperature oxidation mechanism of TiC-based cermets was investigated through an X-ray diffractometer and scanning electron microscope.The added elements Ni and Cr along with their solid solutions not only bond with the hard phase TiC to ensure the physical performance of the cermet,but also impede the internal diffusion during oxidation by forming a dense composite oxide layer,thereby enhancing the oxidation resistance.The TiC-NiCr cermet exhibits a dense protective oxide layer at 900℃ and can endure continuous oxidation for approximately 1000 h.A methodology for fabricating TiC-NiCr metal matrix composites is proposed,and their oxidation resistance is evaluated,providing a theoretical and practical basis for simultaneously enhancing the mechanical properties and oxidation resistance and reducing production costs.
基金National Natural Science Foundation of China(52161009)Innovation Project of Postgraduate Students in North Minzu University(YCX24104)。
文摘To improve the high-temperature oxidation resistance of TiAlNb9 alloy,a Cr-Al-Y co-deposition coating was prepared on the alloy surface by the pack cementation method.The microstructure of the coating was analyzed by scanning electron microscope,energy dispersive spectrometer,and X-ray diffractometer,and the high-temperature oxidation properties of the substrate and coating at 1273 K were compared and studied.The results show that the Cr-Al-Y coating is about 30μm in thickness,and it has a dense structure and good film-substrate bonding.The coating includes an outer layer composed of TiCr_(2),TiCr,Ti_(4)Cr,and(Ti,Nb)Cr_(4) phases as well as an inner layer composed of Ti_(2)Al,and Nb-richγ-TiAl interdiffusion zone.The TiAlNb9 substrate forms an oxide layer composed of TiO_(2) and Al_(2)O_(3) at 1273 K.Due to its loose and porous structure,TiO_(2) oxide film cannot effectively isolate the internal diffusion of element O,resulting in continuous oxidation damage to the substrate.The Cr-Al-Y co-deposition coating forms a dense Cr_(2)O_(3) and Al_(2)O_(3) oxide layer during oxidation,effectively preventing the internal diffusion of element O and significantly improving the high-temperature oxidation resistance of the substrate alloy.
基金Supported by National Natural Science Foundation of China(Grant Nos.52075048,51675058,12232004)Hunan Provincial Excellent Youth Project of the Education Department(Grant No.21B0304)+2 种基金Natural Science Foundation of Hunan Province(Grant No.2023JJ30025)Science and Technology Innovation Program of Hunan Province(Grant No.2023RC1058)Scientific Research Innovation Project for Graduate Student of Changsha University of Science and Technology(Grant No.CLSJCX22096)。
文摘The high-temperature oxidation resistance of AISI 321 stainless steel used in solar thermal power heat exchangers determines its service life.In this study,aluminizing and subsequent laser shock peening(LSP)treatments were employed to improve the high-temperature oxidation resistance of AISI 321 stainless steel at 620°C.These two treatments decreased the oxidation rate of AISI 321 steel.Specifically,the optimal oxidation resistance was observed in aluminized steel before oxidation for 144 h owing to the increased entropy of the LSP-treated specimen.After 144 h,LSP-treated steel achieved the best oxidation resistance because of the formation of a protectiveα-Al2O3film.Moreover,the large amount of subgrain boundaries formed on the aluminized layer of the LSP-treated samples could act as short-circuit paths for the outward diffusion of Al,facilitating the rapid nucleation ofα-Al2O3.Meanwhile,the aluminized layer could isolate the contact between the oxidation environment and matrix,thereby decreasing the oxidation rate.Furthermore,the minimum oxidation parabolic constant was calculated for LSP-treated steel(6.45787×10^(-14)),which was 69.18%and 36.36%that of aluminized and 321 steel,respectively,during the entire oxidation process.Therefore,the combination of aluminizing and LSP treatments can improve the high-temperature oxidation resistance of 321 stainless steel,providing a new idea for its surface treatment to achieve a long service life at high temperatures.
基金financially supported by the National Key Technology R&D Program of China(No.2021YFB3500801)
文摘Enhancing the activity of photocatalysts is a critical challenge for improving the photocatalytic degradation of contaminated wastewater.Here,a novel Ce single-atom-doped titanate nanotube photocatalyst(CeH_(2)Ti_(2)O_(5)·H_(2)O)was successfully synthesized using a onepot solvothermal method.Degradation experiments revealed that the optimal Ce doping ratio was 1.0%.The ultraviolet-visible diffuse reflectance spectroscopy results showed that the bandgap of the Ce-doped sample decreased from 3.02 to 2.87 eV,enhancing the absorption in the visible spectral range.At the same time,the BrunauerEmmett-Teller specific surface area increased from 63.68 to 88.95 m^(2)g^(-1).The 1.0%Ce-H_(2)Ti_(2)O_(5)·H_(2)O(HTC_(1))could degrade 99.04%of 100 mg L-1rhodamine B(RhB)after 40 min of visible-light irradiation.The degradation efficiency decreased by only 21.24%after five cycles.The results of free-radical quenching and electron spin resonance spectroscopy analyses indicated that HTC_(1)achieved efficient degradation of RhB through a direct hole oxidation mechanism.Compared with pure protonated titanate nanotubes(H_(2)Ti_(2)O_(5)·H_(2)O),HTC_(1)had a higher specific surface area,more electron traps,narrower bandgap,longer hole lifetime,and suppressed photogenerated charge recombination rate owing to the Ce single-atom doping.
基金supported by the National Natural Science Foundation of China(22288102)。
文摘The large molecular weight and high hydrophilicity of chloramphenicol(CAP) residuals in wastewater led to severe degradation difficulty,which propelled the development of new wastewater degradation processes and reactors based on process intensification.This study enhanced the CAP degradation by ozone/peroxydisulfate(PDS) advanced oxidation process in a submerged rotating packed bed(SRPB)reactor.Compared the usage of different oxidants,it was indicated that the combination of O_(3) and PDS exhibited a higher degradation efficiency than ozone and PDS alone.The more desired degradation efficiency could be achieved at the operating conditions of ascending PDS concentration,SRPB rotational speed,ozone concentration,reduced initial CAP concentration,and the water qualities of ascended pH,lower Cl^(-)and initial CO_(3)^(2-) concentrations.Under the optimized conditions of C_(CAP)=20 mg·L^(-1),C_(O3)=30 mg·L^(-1),C_(PDS)=100 mg·L^(-1),and N=400 r·min^(-1),and water qualities of pH=10,the maximum chloramphenicol degradation efficiency of 97% and kinetic constant of 0.23 min^(-1) were achieved after treating 16 min.A comparison of the results with previously reported advanced oxidation processes of CAP indicated that the enhanced O^(3)/PDS advanced oxidation system using the SRPB can significantly improve the degradation efficiency of CAP.
基金supported by the University Synergy Innovation Program of Anhui Province(Grant Nos.GXXT-2023-025 and GXXT-2023-026)Natural Science Foundation of Anhui Province(Grant Nos.2008085ME149,2308085QE132 and 2308065ME171)Anhui University Scientific Research Project(Grant Nos.2022AH040247,2023AH051660,2023AH051670 and 2023AH051671).
文摘To improve the high-temperature service properties of coppery tuyere,Co06 coating with a Ni60A interlayer was prepared on copper by plasma cladding.Ni60A interlayer acted as a bridge to promote the element diffusion,thus achieving metallurgical bonding.Due to the strengthening effect ofγ-Co,Cr_(23)C_(6)and Cr_(7)C_(3)phases,the wear resistance of Co06–Ni60A coating was much higher than that of copper substrate.As the temperature increased,the wear resistance of coating decreased first and then increased.The coating exhibited better wear resistance at 600℃ due to the oxidation wear mechanism.Compared with copper substrate and Ni60A,the oxidation resistance of Co06 was increased by 6.0 and 1.9 times,respectively.For melting loss resistance,Co06–Ni60A coating was superior to Ni60A single-layer coating,but the molten iron can still form a micro-metallurgical bonding with the coating surface.
基金supported by the Natural Science Foundation of Inner Mongolia Autonomous Region of China(Grant No.2024LHMS05048).
文摘Addressing the growing challenge of water contamination,this study comparatively evaluated a persulfate(PDS)system activated by nonradical nitrogen-doped carbon nanotubes(N-CNTs)versus a PDS system activated by radical-based iron(Fe^(2+)),both used for the degradation of bisphenol A(BPA).The N-CNTs/PDS system,driven by the electron transfer mechanism,achieved remarkable 90.9%BPA removal within 30 min at high BPA concentrations,significantly outperforming the Fe^(2+)/PDS system,which attained only 38.9%removal.The N-CNTs/PDS system maintained robust degradation efficiency across a wide range of BPA concentrations and exhibited a high degree of resilience in diverse water matrices.By directly abstracting electrons from BPA molecules,the N-CNTs/PDS system effectively minimised oxidant wastage and mitigated the risk of secondary pollution,ensuring efficient utilisation of active sites on N-CNTs and sustaining a high catalytic rate.The formation of the N-CNTs-PDS^(*)complex significantly enhanced BPA degradation and mineralisation,thereby optimising PDS consumption.These findings highlight the unparalleled advantages of the N-CNTs/PDS system in managing complex wastewater,offering a promising and innovative solution for treating complex industrial wastewater and advancing environmental remediation efforts.
基金Project(GC13A113)supported by the Technology Research and Development Program of Heilongjiang Provincial Science and Technology DepartmentProject(12511469)supported by Heilongjiang Provincial Science and Technology Department
文摘Ni-La2O3/CeO2 composite films were prepared by electrodeposition from a nickel sulfate bath containing certain content of micrometer and nanometer La2O3/CeO2 particles. The effect of La2O3 or CeO2 particle size on the oxidation resistance of the electrodeposited Ni-La2O3/CeO2 composites in air at 1000 °C was studied. The results indicate that, compared with the electrodeposited Ni-film, Ni-La2O3/CeO2 composites exhibit a superior oxidation resistance due to the codeposited La2O3 or CeO2 particles blocking the outward diffusion of nickel. Moreover, compared with nanoparticles, La2O3 or CeO2 microparticles have stronger effect because La2O3 or CeO2 microparticles also act as a diffusion barrier layer at the onset of oxidation.
基金supported by the National Natural Sci-ence Foundation of China(No.40830527,40771102)the New Century Excellent Talents in University of China(No.NCET-09-0399)
文摘Manganese oxides are known as one type of semiconductors,but their photocatalysis characteristics have not been deeply explored.In this study,photocatalytic degradation of phenol using several synthesized manganese oxides,i.e,acidic birnessite （BIR-H）,alkaline birnessite （BIR-OH）,cryptomelane （CRY） and todorokite （TOD）,were comparatively investigated.To elucidate phenol degradation mechanisms,X-ray diffraction （XRD）,ICP-AES （inductively coupled plasma-atomic emission spectroscopy）,TEM （transmission electronic microscope）,N 2 physisorption at 77 K and UV-visible diffuse reflectance spectroscopy （UV-Vis DRS） were employed to characterize the structural,compositional,morphological,specific surface area and optical absorption properties of the manganese oxides.After 12 hr of UV-Vis irradiation,the total organic carbon （TOC） removal rate reached 62.1%,43.1%,25.4%,and 22.5% for cryptomelane,acidic birnessite,todorokite and alkaline birnessite,respectively.Compared to the reactions in the dark condition,UV- Vis exposure improved the TOC removal rates by 55.8%,31.9%,23.4% and 17.9%.This suggests a weak ability of manganese oxides to degrade phenol in the dark condition,while UV-Vis light irradiation could significantly enhance phenol degradation.The manganese minerals exhibited photocatalytic activities in the order of：CRY BIR-H TOD BIR-OH.There may be three possible mechanisms for photochemical degradation：（1） direct photolysis of phenol;（2） direct oxidation of phenol by manganese oxides;（3） photocatalytic oxidation of phenol by manganese oxides.Photocatalytic oxidation of phenol appeared to be the dominant mechanism.
基金Project supported by the Science Technology Foundation of Educational Department(No.204020).
文摘The 2,4,6-trinitrotoluene （TNT） is a potential carcinogens and TNT contaminated wastewater, which could not be effectively disposed with conventional treatments. The supercritical water oxidation （SCWO） to treat TNT contaminated wastewater was studied in this article, The TNT concentration in wastewater was measured by high-performance liquid chromatograph （HPLC） and the degraded intermediates were analyzed using GC-MS. The results showed that SCWO could degrade TNT efficiently in the presence of oxygen. The reaction temperature, pressure, residence time and oxygen excess were the main contributing factors in the process. The decomposition of TNT was accelerated as the temperature or residence time increased. At 550℃, 24 MPa, 120 s and oxygen excess 300%, TNT removal rate could exceed 99.9%. Partial oxidation occured in SCWO without oxygen. It was concluded that supercritical water was a good solvent and had excellent oxidation capability in the existence of oxygen. The main intermediates of TNT during SCWO included toluene, 1,3,5-trinitrobenzene, nitrophenol, naphthalene, fluorenone, dibutyl phthalate, alkanes and several dimers based on the intermediate analysis. Some side reactions, such as coupled reaction, hydrolysis reaction and isomerization reaction may take place simultaneously when TNT was oxidized by SCWO.
基金The Hi Tech Research and Development Program(863) of China(No. 2002AA649090) and the National Basic Research Program(973) of China(No.2003CB415006)
文摘A novel process, microwave assisted catalytic wet air oxidation(MW-CWO), was applied for the degradation of H-acid(1-amino-8-naphthol-3, 6-disulfonic acid) in aqueous solution. Ni-loaded granular activated carbon(GAC), prepared by immersion-calcination method, was used as catalyst. The results showed that the MW-CWO process was very effective for the degradation of H-acid in aqueous solution under atmospheric pressure with 87.4% TOC (total organic carbon) reduction in 20 min. Ni on GAC existed in the form of NiO as specified by XRD. Loss of Ni was significant in the initial stage, and then remained almost constant after 20 min reaction. BET surface area results showed that the surface property of GAC after MW-CWO process was superior to that of blank GAC.
基金Supported by the Key Technologies R&D Program of China(2011BAE111300)
文摘The degradation capacity of advanced oxidants generated from oxygen reduction was investigated in model effluent containing chlorobenzene, aniline and benzene through the advanced oxidation processes(AOPs). Intermediate products of the degradation process were determined by GC–MS, and they contributed to specify the degradation pathways of monoaromatic compounds. The study particularly focused on the influence of the dosage of the oxidant, pH and the initial concentration of organic compounds on the degradation effectiveness.When the dosage of oxidant was 4 wt% and the pH was 7, the maximum degradation rates of 74.83% chlorobenzene, 70.32% aniline and 37.69% benzene were achieved. Furthermore, microwave was applied to intensify the oxidation process under optimal operation conditions, and the degradation rates were increased to 87.85% chlorobenzene, 89.11% aniline and 39.03% benzene, respectively.
基金financially supported by the National Natural Science Foundation of China and Shanghai Baosteel Group Company(No. U1960204)the National Natural Science Foundation of China(Nos. 51871042 and 51501034)the Fundamental Research Funds for the Central Universities (No. N2023026)。
文摘The oxidation behavior and mechanism of as-received and 30 % cold-rolled alumina-forming austenitic(AFA) steel were investigated in dry air at 700℃.The results show that the mass gain per unit area curves of as-received and 30 % cold-rolled steels subject to near-parabolic law before 100 h oxidation time.Two samples both show higher high-temperature oxidation resistance due to the formation of dense Al_(2)O_(3) oxide scale.Gradual spallation of outer scale results in the formation of continuous and dense alumina scale.Dislocations can act as short-circuit diffusion channel for the diffusion of Al from alloy matrix to surface,and also provide nucleation sites for B2-NiAl phase,which ensure the continuous formation of Al_(2)O_(3) scale.
基金This work was financially supported by the National Natural Science Foundation of China(No.52071014)the Fundamental Research Funds for the Central Universities(No.FRF-GF-19-033BZ)the National Key Research and Development Program of China(No.2020YFB0704501).
文摘High-temperature oxidation is a common failure in high-temperature environments,which widely occur in aircraft engines and aerospace thrusters;as a result,the development of anti-high-temperature oxidation materials has been pursued.Ni-based alloys are a common high-temperature material;however,they are too expensive.High-entropy alloys are alternatives for the anti-oxidation property at high temperatures because of their special structure and properties.The recent achievements of high-temperature oxidation are reviewed in this paper.The high-temperature oxidation environment,temperature,phase structure,alloy elements,and preparation methods of high-entropy alloys are summarized.The reason why high-entropy alloys have anti-oxidation ability at high temperatures is illuminated.Current research,material selection,and application prospects of high-temperature oxidation are introduced.
基金the National Natural Science Foundation of China(Nos.51878325,51868050,51622806,51378246 and 51720105001)the Natural Science Foundation of Jiangxi Province(Nos.20162BCB22017,20165BCB18008,20171ACB20017,20133ACB21001 and 20171BAB206049)the Graduate Innovation Fund of Jiangxi Province(No.YC2018-S360)。
文摘Herein,we prepa red novel three-dimensional(3D)gear-s haped Co3O4@C(Co3O4 modified by amorphous carbon)and sheet-like SnO2/CC(SnO2 grow on the carbon cloth)as anode and cathode to achieve efficient removal of 4-nitrophenol(4-NP)in the presence of peroxymonosulfate(PMS)and simultaneous electrocatalytic reduction of CO2,respectively.In this process,4-NP was mineralized into CO2 by the Co3O4@C,and the generated CO2 was reduced into HCOOH by the sheet-like SnO2/CC cathode.Compared with the pure Co0.5(Co3O4 was prepared using 0.5 g urea)with PMS(30 mg,0.5 g/L),the degradation efficiency of 4-NP(60 mL,10 mg/L)increased from 74.5%-85.1%in 60 min using the Co0.5 modified by amorphous carbon(Co0.5@C).Furthermore,when the voltage of 1.0 V was added in the anodic system of Co0.5@C with PMS(30 mg,0.5 g/L),the degradation efficiency of 4-NP increased from 85.1%-99.1%when Pt was used as cathode.In the experiments of 4-NP degradation coupled with simultaneous electrocatalytic CO2 reduction,the degradation efficiency of 4-NP was 99.0%in the anodic system of Co0.5@C with addition of PMS(30 mg,0.5 g/L),while the Faraday efficiency(FE)of HCOOH was 24.1%at voltage of-1.3 V using the SnO2/CC as cathode.The results showed that the anode of Co3O4 modified by amorphous carbon can markedly improve the degradation efficiency of 4-NP,while the cathode of SnO2/CC can greatly improve the FE and selectivity of CO2 reduction to HCOOH and the stability of cathode.Finally,the promotion mechanism was proposed to explain the degradation of organic pollutants and reduction of CO2 into HCOOH in the process of electrocatalysis coupled with advanced oxidation processes(AOPs)and simultaneous CO2 reduction.
基金Item Sponsored by Special Fund of Jiangsu Province of China for Transformation of Scientific and Technological Achievements (BA2010053)
文摘The kinetic curve of the high-temperature oxidation of austenitie stainless steel Crl8Ni11 Cu3Al3MnNb at different temperatures was measured by weighting method. It is showed that the oxidation curves at 700 and 800 ℃ followed the parabolic law, and the steel presented an excellent anti-oxidation. The surface morphology and structure of the oxide film were studied by scanning electron microscopy and X-ray diffraction methods. A dense oxide film was attained at 700 and 800 ℃, mainly composed of the hexagonal Al2 O3, Fe2 O3, and a small amount oxide of Cr at 700 ℃. At 900 ℃ the oxide film started to delaminate, and was composed of （Cr,Fe）2O3 and the spinel CuCrMnO4 and Fe（Cr, Al） 2O3.
