A novel type of microcapsule-encapsulated corrosion inhibitor was prepared in a water-based solution with a pH range of 7-8,and it was applied to the composite organic coating of magnesium alloy plasma electrolytic ox...A novel type of microcapsule-encapsulated corrosion inhibitor was prepared in a water-based solution with a pH range of 7-8,and it was applied to the composite organic coating of magnesium alloy plasma electrolytic oxidation to enhance its corrosion resistance and self-healing properties.The morphology,chemical composition,structure,and functional properties of the composite coating were investigated by scanning electron microscopy(SEM),energy dispersive X-ray spectroscopy(EDS),Fourier transform infrared spectroscopy(FTIR),polarization curve,alternating current impedance,and salt immersion test.The experimental results showed that,after immersion in a 3.5 wt%NaCl solution for 12 h,the coating could effectively protect AZ91D from corrosion.When the coating was damaged,the exposed alloy surface would release metal ions in the corrosive environment and react with the corrosion inhibitor 8-hydroxyquinoline to form a Mg(8-HQ)_(2) chelate,exhibiting significant self-healing behavior.The study results demonstrate the broad application prospects of microcapsule technology in the coating field,providing new ideas for the development of efficient anti-corrosion coatings.展开更多
Vanadium‐chromium oxides(VCrO)were usually prepared by high‐temperature solid‐state reactions;however,mixed phases were frequently produced and the morphology of the products was not well controlled.In this work,we...Vanadium‐chromium oxides(VCrO)were usually prepared by high‐temperature solid‐state reactions;however,mixed phases were frequently produced and the morphology of the products was not well controlled.In this work,we prepared amorphous VCrO precursors by using V2O5 and CrO3 and alcohols or mixtures of alcohol and water via solvothermal reaction at 180°C.The precursors were then calcined under nitrogen at various temperatures.The products were characterized by powder X‐ray diffraction,transmission electron microscopy,and X‐ray photoelectron spectroscopy.It was revealed that pure‐phase nanocrystalline orthorhombic CrVO4 was obtained when methanol or methanol/water was used as the solvothermal medium and the precursor was calcined at 700°C.The size of the CrVO4 crystals was around 500 nm when methanol was used,whereas it reduced significantly to less than 50 nm when a mixture of methanol and water was used.The sizes could be effectively tuned from 10 to 50 nm by varying the methanol/water volume ratio.To the best of our knowledge,this is the first report on the synthesis of pure‐phase CrVO4 nanocrystals.The nano‐CrVO4 showed almost the highest catalytic activity for the ammoxidation of 2,6‐dichlorotoluene to 2,6‐dichlorobenzonitrile among the reported bi‐component composite oxides,owing to its smaller particle size,larger specific surface area,and more exposed active centers.展开更多
A coating of composition Si-40Mo (wt pct) was prepared by fused slurry coating method on the two-dimensional carbon/carbon (2D-C/C) composite to improve oxidation resistance. In the procedure of the fabrication, pure ...A coating of composition Si-40Mo (wt pct) was prepared by fused slurry coating method on the two-dimensional carbon/carbon (2D-C/C) composite to improve oxidation resistance. In the procedure of the fabrication, pure St slurry inner layer in the pre-coating was necessary to apply because of infiltration of liquid Si into the substrate during the sintering. The coating consists of Si continuous phase and MoSi2 particles. In addition, the infiltration of Si into the substrate and the SiC reaction layer between the coating and the C/C composite were observed. Oxidation behavior of coated and uncoated C/C composites was studied in cyclic mode. The oxidation resistance and the thermal shock resistance of the Si-Mo fused slurry coating were quite excellent at 1370℃.展开更多
A series of novel Ni/CeOe-Al2O3 composite catalysts were synthesized by one-step citric acid complex method, The as-synthesized catalysts were characterized by N2 physical adsorption/desorption, X-ray diffraction （XR...A series of novel Ni/CeOe-Al2O3 composite catalysts were synthesized by one-step citric acid complex method, The as-synthesized catalysts were characterized by N2 physical adsorption/desorption, X-ray diffraction （XRD）, Fourier transform infrared （FT-IR） spectroscopy, hydrogen temperature-programmed reduction （Hz-TPR）, X-ray photoelectron spectroscopy （XPS） and thermogravimetry analysis （TGA）. The effects of nickel content, calcination and reaction temperatures, gas hourly space velocity （GHSV） and inert gas dilution of N2 on their performance of catalytic partial oxidation of methane （CPOM） were investigated. Catalytic activity test results show that the highest methane conversion （〉85%）, the best selectivities to carbon monoxide （〉87%） and to hydrogen （〉95%）, the excellent stability and perfect Hz/CO ratio （2.0） can be obtained over Ni/CeO2-Al2O3 with 8 wt% Ni content calcined at 700 ℃ under the reaction condition of 750 ℃, CH4/O2 ratio of 2 ： 1 and gas hourly space velocity of 12000 mL.h-1 .g-1. Characterization results show that the good catalytic performance of this composite catalyst can be contributed to its large specific surface area （~108 m2.g-1）, small crystallite size, easy reducibility and low coking rate.展开更多
Ce_(x)Co_(y)Cuzoxide composite catalysts were prepared by using polyethylene glycol, citrate sol-gel method combined with PMMA template for the oxidation of o-xylene. The catalysts were characterized by the Xray diffr...Ce_(x)Co_(y)Cuzoxide composite catalysts were prepared by using polyethylene glycol, citrate sol-gel method combined with PMMA template for the oxidation of o-xylene. The catalysts were characterized by the Xray diffraction(XRD), H2-temperature programmed reduction(H2-TPR), X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared spectroscopy(FT-IR), etc. The catalytic activity for o-xylene was investigated. The catalytic degradation pathway and mechanism of o-xylene were inferred. The results show that Ce O_(2)is mainly present on the surface of all catalysts. The surface area of Ce_(2)Co1Cu1is up to 77.2 m^(2)/g, and the average pore size is 10.62 nm. It exhibits redox and sufficient Ce^(4+)and Ce^(^(3+)), and reactive oxygen species, and has maximum O-H and C=O in the five catalyst samples. The catalytic activity of Ce2Co1Cu1is the best at low temperature, with the T50and T90values of 235 and 258°C at a space velocity of 32000 h-1, respectively. The o-xylene is oxidized to o-methyl benzaldehyde, and then further oxidized to o-methylbenzoic acid, and finally CO_(2)and H2O are formed.展开更多
Oxidation behavior of C/C-SiC gradient matrix composites and C/C composites were compared in stationary air. The results show that oxidation threshold of C-SiC materials increases with the amount of SiC particles in t...Oxidation behavior of C/C-SiC gradient matrix composites and C/C composites were compared in stationary air. The results show that oxidation threshold of C-SiC materials increases with the amount of SiC particles in the codeposition matrix. Oxidation rate of C/C-SiC gradient matrix composites is significantly lower than that of C/C material. The micro-oxidation process was observed by SEM.展开更多
The fracture toughness of a carbon/carbon composites oxidized at different temperature for 1 h was measured. The fracture surfaces were examined by scanning electron microscopy （SEM）. The results indicate that oxida...The fracture toughness of a carbon/carbon composites oxidized at different temperature for 1 h was measured. The fracture surfaces were examined by scanning electron microscopy （SEM）. The results indicate that oxidation temperature has significant effects on the fracture toughness. Fracture toughness decreases with the increase of the weight loss. The SEM images reveal that the decrease of fracture toughness was mainly attributed to the oxidation of the interface in the composite.展开更多
YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios were deposited on superalloy Inconel 600 by electrophoretic deposition（EPD） technique, followed by sintering in CH_4 atmosphere at 1 100 ℃for 2 h ...YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios were deposited on superalloy Inconel 600 by electrophoretic deposition（EPD） technique, followed by sintering in CH_4 atmosphere at 1 100 ℃for 2 h and isothermally oxidation at 1000 ℃ for 50 h. After sintering at 1100 ℃ for 2 h in CH_4 atmosphere, besides ZrC and t-ZrO_2 phases, the phase constitutes of Ni：Al mole ratios with 1：3, 1：2, and 1：1 were（Zr, Al）C, AlNi_3 and Ni phases, respectively. A remarkable difference in the oxidation behaviors of YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios was observed. For YSZ（Ni：Al=1：3） coated sample, oxidation at 1000 ℃ causes decomposition of the（Zr,Al）C solid solution to metallic Al, and then most of the Al is oxidized to Al_2O_3. For the YSZ（Ni：Al=1：2） coated sample, oxidation at 1000 ℃ mainly causes decomposition of the AlNi_3 phase. For YSZ（Ni：Al=1：1） coated sample, after oxidation at 1000 ℃, most of the Ni is oxidized to Ni O phase, and tolerated 50 h of oxidation and finally cracked and spalled from the specimen. YSZ（Ni：Al=1：3） and YSZ（Ni：Al=1：2） coated samples show superior oxidation resistance than that of YSZ coating. The different oxidation resistance mechanisms of YSZ/（Ni, Al） composite coatings sintered in CH_4 atmosphere were discussed.展开更多
Plasma-coupled catalysis is a promising volatile organic co mpounds(VOCs) removal technology because of its interactional principles of plasma decomposition and catalytic oxidation.However,the problem of harmful by-pr...Plasma-coupled catalysis is a promising volatile organic co mpounds(VOCs) removal technology because of its interactional principles of plasma decomposition and catalytic oxidation.However,the problem of harmful by-products is still in trouble.A series of rare earth doped RE-NiO_(x)(RE=Ce,Y,La) composite oxides were synthesized by metal organic frameworks(MOFs)-derived method for coupled plasma oxidation of benzene and by-product ozone removal.Compared with plasma alone,the 1%La-NiO_(x)catalyst shows the best enhancement of 50% for benzene conversion with complete removal of a maximum of 800 ppm ozone.The energy consumption for 90% benzene removal efficiency(η90%) is also reduced from 3600 to 1200 J/L.Characterization re sults of RE-NiO_(x) catalysts indicate that the doping of La causes interaction and synergistic effect between La and Ni,and the surface oxygen and lattice oxygen with defects play crucial roles in benzene oxidation and ozone decomposition,respectively.In addition,the decomposition mechanism of benzene and ozone under plasma is proposed.Plasma is responsible for the indiscriminate bond breaking in benzene and oxygen to form a variety of organic intermediates and ozone,while the La-NiO_(x) catalyst selectively oxidizes the intermediates to CO_(x)/H2O and decomposes the ozone into oxygen.展开更多
SiCp/Al2O3-Al composites were synthesized by means of direct metal oxidation method. The composition and microstructures of the composites were investigated using X-ray diffraction （XRD）, scanning electron microsco...SiCp/Al2O3-Al composites were synthesized by means of direct metal oxidation method. The composition and microstructures of the composites were investigated using X-ray diffraction （XRD）, scanning electron microscopy （SEM） and metallurgical microscope. The effects of technical parameters on the properties of the product were analyzed. The results indicate that the composite possesses a dense microstructure, composed of three interpenetrated phases. Of them, SiO2 layer prohibits the powdering of the composites; Mg promotes the wetting and infiltration of the system and Si restricts the interfacial reaction while improving the wetting ability between reinforcement and matrix.展开更多
Sodium-ion batteries have garnered significant attention as a cost-effective alternative to lithium-ion batteries due to the abundance and affordability of sodium precursors.However,the lack of suitable electrode mate...Sodium-ion batteries have garnered significant attention as a cost-effective alternative to lithium-ion batteries due to the abundance and affordability of sodium precursors.However,the lack of suitable electrode materials with both high capacity and excellent stability continues to hinder their practical viability.Herein,we couple lattice strain and sulfur deficiency effects in a tin monosulfide/reduced graphene oxide composite to enhance sodium storage performance.Experimental results and theoretical calculations reveal that the synergistic effects of lattice strain and sulfur vacancies in tin monosulfide promote rapid(de)intercalation near the surface/edge of the material,thereby enhancing its pseudocapacitive sodium storage properties.Consequently,the strained and defective tin monosulfide/reduced graphene oxide composite demonstrates a high reversible capacity of 511.82 mAh g^(-1) at 1 A g^(-1) and an outstanding rate capability of 450.60 mAh g^(-1) at 3 A g^(-1).This study offers an effective strategy for improving sodium storage performance through lattice strain and defect engineering.展开更多
The high band gap of zinc oxide(ZnO)has significantly limited its potential application for organic contaminant removal in photocatalysis.In this study,ZnO/halloysites(HNTs)composites(ZnO/HNTs)were prepared using a hi...The high band gap of zinc oxide(ZnO)has significantly limited its potential application for organic contaminant removal in photocatalysis.In this study,ZnO/halloysites(HNTs)composites(ZnO/HNTs)were prepared using a high-temperature calcination method to enhance the removal of tetracycline hydrochloride(TCH).The experimental results demonstrated that the band gap of ZnO/HNTs decreased to 3.12 eV,compared to 3.21 eV for pure ZnO.The observed removal rate(k_(obs))of TCH in the ZnO/HNTs/vis system was 1.90×10^(-2) min^(-1),significantly higher than the rates in the HNTs/vis(1.25×10^(-3)min^(-1))and ZnO/vis(1.13×10^(-2) min^(-1))systems.Additionally,ZnO/HNTs exhibited strong resistance to coexisting natural organic and inorganic matter,maintaining high pollutant removal efficiency in natural water samples.The ZnO/HNTs/vis system also effectively removed other common organic pollutants,such as ciprofloxacin and methylene blue.Cycle tests indicated that the ZnO/HNTs/vis system retained 65.57%of its original efficiency,demonstrating good reusability and versatility.Scavenging and electron paramagnetic resonance experiments identified that h+was the primary species in the ZnO/HNTs/vis system,with other species playing auxiliary roles in TCH degradation.This study provides valuable insights into the design of novel ZnO-based photocatalysts for the degradation of organic pollutants in water.展开更多
Series Li-Sb-Mn composite oxides with different Sb/Mn molar ratios were obtained by solid state reaction.Their structure,morphology and Li^＋ extraction/adsorption properties were characterized by X-ray diffractometry...Series Li-Sb-Mn composite oxides with different Sb/Mn molar ratios were obtained by solid state reaction.Their structure,morphology and Li^＋ extraction/adsorption properties were characterized by X-ray diffractometry （XRD）,scanning electron microscopy （SEM） and atomic absorption spectrophotometry （AAS）,respectively.XRD and SEM analyses reveal that the crystal of the products transfers from spinel to orthorhombic phase with the increase of molar ratio of Sb to Mn from 0.05 to 1.00.The Li^＋ extraction and adsorption experiments for these Li-Sb-Mn composite oxides demonstrate that the composite oxides can all be used as lithium inorganic adsorbents.The acid treated spinel Li-Sb-Mn composite oxide with Sb/Mn molar ratio of 0.05 has a high Li^＋ adsorption capacity of 33.23mg/g in lithium solution.The Sb/Mn molar ratio of these Li-Sb-Mn composite oxides should be a crucial factor in determining their structure and Li^＋ extraction and adsorption properties.展开更多
The composite oxides xAg/Co_（0.93）Ce_（0.07）（x=Ag/（Co＋Ce） molar ratio）,intended for use as high performance catalytic materials,were successfully prepared via citric acid complexation.The effects of silver on ...The composite oxides xAg/Co_（0.93）Ce_（0.07）（x=Ag/（Co＋Ce） molar ratio）,intended for use as high performance catalytic materials,were successfully prepared via citric acid complexation.The effects of silver on the performance of these substances during soot combustion were subsequently investigated.Under O_2,the 0.3Ag/Co_（0.93）Ce_（0.07） catalyst resulted in the lowest ignition temperature,T_（10）,of197 ℃,while the minimum light-off temperature was obtained from both 0.2Ag/Co_（0.93）Ce_（0.07） and0.3Ag/Co_（0.93）Ce_（0.07） in the NO_x atmosphere.These materials were also characterized by various techniques,including H_2,soot and NO_x temperature programmed reduction,X-ray diffraction,and electron paramagnetic resonance,Raman,X-ray photoelectron,and Fourier transform infrared spectroscopic analyses.The results demonstrated that silver significantly alters the catalytic behavior under both O_2 and NO_x,even though the lattice structure of the mixed oxide is not affected.Surface silver oxides generated under the O_2 atmosphere favor soot combustion by participating in the redox cycles between soot and the silver oxide,whereas the AgNO_3 that forms in a NO_x-rich atmosphere facilitates soot abatement at a lower temperature.The inferior activity of AgNO_3 relative to that of Ag_2O results in the different catalytic performance in the presence of NO_x or O_2.展开更多
Cu-Fe composite oxides were prepared by co-precipitation method and tested for higher alcohol synthesis from syngas. The selectivity to C2＋OH and C6＋OH in alcohol distribution was very high while the methane product...Cu-Fe composite oxides were prepared by co-precipitation method and tested for higher alcohol synthesis from syngas. The selectivity to C2＋OH and C6＋OH in alcohol distribution was very high while the methane product fraction in hydrocarbon distribution was rather low, demonstrating a promising potential in higher alcohols synthesis from syngas. The distribution of alcohols and hydrocarbons approximately obeyed Anderson-Schulz-Flory distribution with similar chain growth probability, indicating alcohols and hydrocarbons derived from the same intermediates. The effects of Cu/Fe molar ratio, reaction temperature and gas hourly space velocity （GHSV） on catalytic performance were studied in detail. The sample with a Cu/Fe molar ratio of 10/1 exhibited the best catalytic performance. Higher reaction temperature accelerated water-gas-shift reaction and led to lower total alcohols selectivity. GHSV showed great effect on catalytic performance and higher GHSV increased the total alcohol selectivity, indicating there existed visible dehydration reaction of alcohol into hydrocarbon.展开更多
Mesoporous CeO2-MnOx binary oxides with different Mn/Ce molar ratios were prepared by hydrothermal synthesis and characterized by scanning electron microscopy （SEM）, N2 sorption, X-ray diffraction （XRD）, X-ray pho...Mesoporous CeO2-MnOx binary oxides with different Mn/Ce molar ratios were prepared by hydrothermal synthesis and characterized by scanning electron microscopy （SEM）, N2 sorption, X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and H2 temperature-programmed reduction （H2-TPR）. The characterization results indicated that the CeO2-MnOx catalysts exhibited flower-like microspheres with high specific surface areas, and partial Mn cations could be incorporated into CeO2 lattice to form solid solution. The CeO2-MnOx catalysts showed better catalytic activity for CO oxidation than that prepared by the coprecipitation method. Furthermore, the CeO2-MnOx catalyst with Mn/Ce molar ratio of 1 in the synthesis gel （Ce-Mn-1） exhibited the best catalytic activity, over which the conversion of CO could achieve 90% at 135 ℃. This was ascribed to presence of more Mn species with higher oxida- tion state on the surface and the better reducibility over the Ce-Mn-I catalyst than other CeO2-MnOx catalysts.展开更多
The nano-crystalline Cu-Ce-Zr-O composite oxides were successfully prepared by the supercritical anti-solvent （SAS） process. The physicochemical properties and catalytic performances were investigated by X-ray diffr...The nano-crystalline Cu-Ce-Zr-O composite oxides were successfully prepared by the supercritical anti-solvent （SAS） process. The physicochemical properties and catalytic performances were investigated by X-ray diffraction （XRD）, Raman spectroscopy, H2 temperature-programmed reduction （H2 -TPR）, oxygen storage capacity （OSC） measurement and catalytic activity evaluation. It was found that Cu2＋ ions incorporated into CeO2 -ZrO2 lattice to form Cu-Ce-Zr-O solid solution associated with the formation of oxygen vacancies. The Cu-Ce-Zr-O catalysts prepared via the SAS process with the Cu content 2.63 mol.% showed the highest OSC index of 636.9 μmol/g. Compared with the samples prepared by impregnation method, Cu doping using SAS process could improve the dispersion of Cu2＋ in the composite oxide, enhance the interaction between Cu2＋ and CeO2-ZrO2 , improve the reducibility of catalyst, and thus improve the OSC performance and increase the catalytic activity for CO oxidation at low temperature.展开更多
The hydrogen permeation resistance of Si–Zr(SZ) and Si–Al(SA) composite sol oxide coating on zirconium hydride blocks(Zr H) was studied. SZ and SA composite sol were prepared by sol–gel method. SZ and SA composite ...The hydrogen permeation resistance of Si–Zr(SZ) and Si–Al(SA) composite sol oxide coating on zirconium hydride blocks(Zr H) was studied. SZ and SA composite sol were prepared by sol–gel method. SZ and SA composite oxide coatings were prepared on the surface of Zr H(in situ oxidized or not) in turns by dip-coating and heat treatment. Hydrogen permeation of Zr Hwith and without composite oxide coating was compared.Hydrogen desorption experiments in thermal vacuum show that hydrogen permeation resistance of SA composite oxide coating is better than that of SZ, to a certain extent,which could decrease hydrogen thermal loss. Experimental results in the working condition show that the SA composite oxide coating can not only prevent hydrogen permeation, but also retard contact and reaction between COand Zr Hmatrix, which could mitigate excessive oxidation of in situ oxide film. Differential scanning calorimetry and thermogravimetry(DSC–TG) analysis was performed to investigate the decomposition behavior of SA and SZ liquid sol in heat treatment process. X-ray diffraction(XRD) and scanning electron microscopy(SEM) analysis were employed to characterize the phase composition,surface and cross-section morphology of the coatings.展开更多
HZSM-5, Al_2O_3, TiO_2 and SiO_2 supported CeO_2-ZrO_2-CrO_x catalysts were prepared by deposition-precipitation method and tested for deep catalytic oxidation of 1,2-dichloroethane（DCE）, as one of the common chlori...HZSM-5, Al_2O_3, TiO_2 and SiO_2 supported CeO_2-ZrO_2-CrO_x catalysts were prepared by deposition-precipitation method and tested for deep catalytic oxidation of 1,2-dichloroethane（DCE）, as one of the common chlorinated organic pollutants. All the catalysts were characterized by means of N_2 adsorption-desorption, X-ray photoelectron spectroscopy（XPS）, ammonia-temperatureprogrammed desorption（NH_3-TPD） and hydrogen temperature-programmed reduction（H2-TPR）. The characterization results revealed that there was strongly synergistic effect between the oxidizability of CZCr species and the acidity of supports, which obviously promoted the catalytic activity for DCE degradation. 20% CZCr/HZSM-5 showed the highest activity and good durability during the long-term continuous test. The catalytic activity decreased in the order： 20%CZCr/HZSM-5〉CZCr〉20%CZCr/TiO_2〉20%CZCr/Al_2O_3〉20%CZCr/SiO_2.展开更多
Iron-manganese composited oxide（FeMnO） was prepared with potassium permanganate and ferrous salt. Interface performance, charge property and structure topography of the FeMnO were investigated. Coagulation efficienc...Iron-manganese composited oxide（FeMnO） was prepared with potassium permanganate and ferrous salt. Interface performance, charge property and structure topography of the FeMnO were investigated. Coagulation efficiency and pollution removal mechanism of the FeMnO were approached. Results show that the main compositions of the FeMnO are δ-manganese dioxide and ferric hydroxide. The specific surface area is about 146.22 m^2/g. The FeMnO contains rich hydroxyl with extremely strong adsorption action and chemical adsorption activity. The zero charge point of the oxide in pure water is about 8.0 of pH value. Under neutral pH value conditions, the FeMnO particle surface carried positive charges. The FeMnO particles are quasi-spherical micro-particles with irregular sizes adjoined each other to form net construction. Phosphorus removal efficiency of the FeMnO is remarkable, the total dissoluble phosphorus of settled water can be reduced below detecting level（0.3 μtg/L） at a FeMnO dosage of 6 mg/L, and total phosphorus below detecting level at a FeMnO dosage of 10 mg/L, for water samples containing total phos- phorus of 1281.70 μg/L and total dissoluble phosphorus of 1187.91 μtg/L. The mechanism of effective coagulation for phosphorus removal is combined results of multiple actions of adsorption, charge neutralization, adsorption/bridging and so on.展开更多
基金Funded by the National Natural Science Foundation of China(No.52271066)Basic Research and Innovation Project for Vehicle Power+1 种基金Key Project of"Two-Chain Integration"in Shaanxi Province(No.2023-LL-QY-33-3)Xi'an Key Laboratory of Corrosion Protection and Functional Coating Technology for Military and Civil Light Alloy and Key Project of Shaanxi Natural Science Foundation Research Program(No.2021JZ-54)。
文摘A novel type of microcapsule-encapsulated corrosion inhibitor was prepared in a water-based solution with a pH range of 7-8,and it was applied to the composite organic coating of magnesium alloy plasma electrolytic oxidation to enhance its corrosion resistance and self-healing properties.The morphology,chemical composition,structure,and functional properties of the composite coating were investigated by scanning electron microscopy(SEM),energy dispersive X-ray spectroscopy(EDS),Fourier transform infrared spectroscopy(FTIR),polarization curve,alternating current impedance,and salt immersion test.The experimental results showed that,after immersion in a 3.5 wt%NaCl solution for 12 h,the coating could effectively protect AZ91D from corrosion.When the coating was damaged,the exposed alloy surface would release metal ions in the corrosive environment and react with the corrosion inhibitor 8-hydroxyquinoline to form a Mg(8-HQ)_(2) chelate,exhibiting significant self-healing behavior.The study results demonstrate the broad application prospects of microcapsule technology in the coating field,providing new ideas for the development of efficient anti-corrosion coatings.
基金supported by the National Natural Science Foundation of China(21172269)Innovation Group of Hubei Natural Science Foundation(2018CFA023)Opening Project of Key Laboratory of Optoelectronic Chemical Materials and Devices,Ministry of Education,Jianghan University(JDGD-201809)~~
文摘Vanadium‐chromium oxides(VCrO)were usually prepared by high‐temperature solid‐state reactions;however,mixed phases were frequently produced and the morphology of the products was not well controlled.In this work,we prepared amorphous VCrO precursors by using V2O5 and CrO3 and alcohols or mixtures of alcohol and water via solvothermal reaction at 180°C.The precursors were then calcined under nitrogen at various temperatures.The products were characterized by powder X‐ray diffraction,transmission electron microscopy,and X‐ray photoelectron spectroscopy.It was revealed that pure‐phase nanocrystalline orthorhombic CrVO4 was obtained when methanol or methanol/water was used as the solvothermal medium and the precursor was calcined at 700°C.The size of the CrVO4 crystals was around 500 nm when methanol was used,whereas it reduced significantly to less than 50 nm when a mixture of methanol and water was used.The sizes could be effectively tuned from 10 to 50 nm by varying the methanol/water volume ratio.To the best of our knowledge,this is the first report on the synthesis of pure‐phase CrVO4 nanocrystals.The nano‐CrVO4 showed almost the highest catalytic activity for the ammoxidation of 2,6‐dichlorotoluene to 2,6‐dichlorobenzonitrile among the reported bi‐component composite oxides,owing to its smaller particle size,larger specific surface area,and more exposed active centers.
文摘A coating of composition Si-40Mo (wt pct) was prepared by fused slurry coating method on the two-dimensional carbon/carbon (2D-C/C) composite to improve oxidation resistance. In the procedure of the fabrication, pure St slurry inner layer in the pre-coating was necessary to apply because of infiltration of liquid Si into the substrate during the sintering. The coating consists of Si continuous phase and MoSi2 particles. In addition, the infiltration of Si into the substrate and the SiC reaction layer between the coating and the C/C composite were observed. Oxidation behavior of coated and uncoated C/C composites was studied in cyclic mode. The oxidation resistance and the thermal shock resistance of the Si-Mo fused slurry coating were quite excellent at 1370℃.
基金supported by the National Natural Science Foundation of China(Grants No.21067004 and No.21263005)the Technological Foundation of Jiangxi Province Education Office(No.GJJ12344)+1 种基金the Young Science and Technolgy Project of Jiangxi Province(No.20133BAB21003)the Young Scientist Training Project of Jiangxi Province(No.20122BCB23015)
文摘A series of novel Ni/CeOe-Al2O3 composite catalysts were synthesized by one-step citric acid complex method, The as-synthesized catalysts were characterized by N2 physical adsorption/desorption, X-ray diffraction （XRD）, Fourier transform infrared （FT-IR） spectroscopy, hydrogen temperature-programmed reduction （Hz-TPR）, X-ray photoelectron spectroscopy （XPS） and thermogravimetry analysis （TGA）. The effects of nickel content, calcination and reaction temperatures, gas hourly space velocity （GHSV） and inert gas dilution of N2 on their performance of catalytic partial oxidation of methane （CPOM） were investigated. Catalytic activity test results show that the highest methane conversion （〉85%）, the best selectivities to carbon monoxide （〉87%） and to hydrogen （〉95%）, the excellent stability and perfect Hz/CO ratio （2.0） can be obtained over Ni/CeO2-Al2O3 with 8 wt% Ni content calcined at 700 ℃ under the reaction condition of 750 ℃, CH4/O2 ratio of 2 ： 1 and gas hourly space velocity of 12000 mL.h-1 .g-1. Characterization results show that the good catalytic performance of this composite catalyst can be contributed to its large specific surface area （~108 m2.g-1）, small crystallite size, easy reducibility and low coking rate.
基金Project supported by the Zhejiang Provincial Natural Science Foundation of China (LY20E080003)。
文摘Ce_(x)Co_(y)Cuzoxide composite catalysts were prepared by using polyethylene glycol, citrate sol-gel method combined with PMMA template for the oxidation of o-xylene. The catalysts were characterized by the Xray diffraction(XRD), H2-temperature programmed reduction(H2-TPR), X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared spectroscopy(FT-IR), etc. The catalytic activity for o-xylene was investigated. The catalytic degradation pathway and mechanism of o-xylene were inferred. The results show that Ce O_(2)is mainly present on the surface of all catalysts. The surface area of Ce_(2)Co1Cu1is up to 77.2 m^(2)/g, and the average pore size is 10.62 nm. It exhibits redox and sufficient Ce^(4+)and Ce^(^(3+)), and reactive oxygen species, and has maximum O-H and C=O in the five catalyst samples. The catalytic activity of Ce2Co1Cu1is the best at low temperature, with the T50and T90values of 235 and 258°C at a space velocity of 32000 h-1, respectively. The o-xylene is oxidized to o-methyl benzaldehyde, and then further oxidized to o-methylbenzoic acid, and finally CO_(2)and H2O are formed.
文摘Oxidation behavior of C/C-SiC gradient matrix composites and C/C composites were compared in stationary air. The results show that oxidation threshold of C-SiC materials increases with the amount of SiC particles in the codeposition matrix. Oxidation rate of C/C-SiC gradient matrix composites is significantly lower than that of C/C material. The micro-oxidation process was observed by SEM.
基金Funded by National Natural Science Foundation of China(No.50702045)the Program for New Century Excellent Talents in University(No.NCET-08-0460)Basic Research Foundation of NWPU(No.JC20100227)
文摘The fracture toughness of a carbon/carbon composites oxidized at different temperature for 1 h was measured. The fracture surfaces were examined by scanning electron microscopy （SEM）. The results indicate that oxidation temperature has significant effects on the fracture toughness. Fracture toughness decreases with the increase of the weight loss. The SEM images reveal that the decrease of fracture toughness was mainly attributed to the oxidation of the interface in the composite.
基金Funded by the Science and Technology Key Fund Project of Shanghai University of Engineering Science(cs1405015)the Graduate Research and Innovation Special Projects of Shanghai University of Engineering Science(15KY0501 and 14KY0515)
文摘YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios were deposited on superalloy Inconel 600 by electrophoretic deposition（EPD） technique, followed by sintering in CH_4 atmosphere at 1 100 ℃for 2 h and isothermally oxidation at 1000 ℃ for 50 h. After sintering at 1100 ℃ for 2 h in CH_4 atmosphere, besides ZrC and t-ZrO_2 phases, the phase constitutes of Ni：Al mole ratios with 1：3, 1：2, and 1：1 were（Zr, Al）C, AlNi_3 and Ni phases, respectively. A remarkable difference in the oxidation behaviors of YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios was observed. For YSZ（Ni：Al=1：3） coated sample, oxidation at 1000 ℃ causes decomposition of the（Zr,Al）C solid solution to metallic Al, and then most of the Al is oxidized to Al_2O_3. For the YSZ（Ni：Al=1：2） coated sample, oxidation at 1000 ℃ mainly causes decomposition of the AlNi_3 phase. For YSZ（Ni：Al=1：1） coated sample, after oxidation at 1000 ℃, most of the Ni is oxidized to Ni O phase, and tolerated 50 h of oxidation and finally cracked and spalled from the specimen. YSZ（Ni：Al=1：3） and YSZ（Ni：Al=1：2） coated samples show superior oxidation resistance than that of YSZ coating. The different oxidation resistance mechanisms of YSZ/（Ni, Al） composite coatings sintered in CH_4 atmosphere were discussed.
基金Project supported by the National Natural Science Foundation of China(22176123,U1832155)the National Key Research&Development Plan(2017YFC0211804).
文摘Plasma-coupled catalysis is a promising volatile organic co mpounds(VOCs) removal technology because of its interactional principles of plasma decomposition and catalytic oxidation.However,the problem of harmful by-products is still in trouble.A series of rare earth doped RE-NiO_(x)(RE=Ce,Y,La) composite oxides were synthesized by metal organic frameworks(MOFs)-derived method for coupled plasma oxidation of benzene and by-product ozone removal.Compared with plasma alone,the 1%La-NiO_(x)catalyst shows the best enhancement of 50% for benzene conversion with complete removal of a maximum of 800 ppm ozone.The energy consumption for 90% benzene removal efficiency(η90%) is also reduced from 3600 to 1200 J/L.Characterization re sults of RE-NiO_(x) catalysts indicate that the doping of La causes interaction and synergistic effect between La and Ni,and the surface oxygen and lattice oxygen with defects play crucial roles in benzene oxidation and ozone decomposition,respectively.In addition,the decomposition mechanism of benzene and ozone under plasma is proposed.Plasma is responsible for the indiscriminate bond breaking in benzene and oxygen to form a variety of organic intermediates and ozone,while the La-NiO_(x) catalyst selectively oxidizes the intermediates to CO_(x)/H2O and decomposes the ozone into oxygen.
基金National Natural Science Foundation of China (50372037)Scientific Research Foundations of Shaanxi University of Science and Technology (SUST-B14)
文摘SiCp/Al2O3-Al composites were synthesized by means of direct metal oxidation method. The composition and microstructures of the composites were investigated using X-ray diffraction （XRD）, scanning electron microscopy （SEM） and metallurgical microscope. The effects of technical parameters on the properties of the product were analyzed. The results indicate that the composite possesses a dense microstructure, composed of three interpenetrated phases. Of them, SiO2 layer prohibits the powdering of the composites; Mg promotes the wetting and infiltration of the system and Si restricts the interfacial reaction while improving the wetting ability between reinforcement and matrix.
基金supported by the National Natural Science Foundation of China(no.22109023,no.22179022,and no.22209027)the Youth Innovation Fund of Fujian Province(no.2021J05043 and no.2022J05046)+5 种基金the National Key Research and Development Program of China(2023YFC3906300)the FuXiaQuan National Independent Innovation Demonstration Zone Collaborative Innovation Platform(no.2022-P-027)the·“Hundred Talents·Plan”of Fujian Provincethe“Top Young Talents of Young Eagle”Program of Fujian Provincethe Award Program for Fujian Minjiang Scholar Professorshipthe Talent Fund Program of Fujian Normal University.
文摘Sodium-ion batteries have garnered significant attention as a cost-effective alternative to lithium-ion batteries due to the abundance and affordability of sodium precursors.However,the lack of suitable electrode materials with both high capacity and excellent stability continues to hinder their practical viability.Herein,we couple lattice strain and sulfur deficiency effects in a tin monosulfide/reduced graphene oxide composite to enhance sodium storage performance.Experimental results and theoretical calculations reveal that the synergistic effects of lattice strain and sulfur vacancies in tin monosulfide promote rapid(de)intercalation near the surface/edge of the material,thereby enhancing its pseudocapacitive sodium storage properties.Consequently,the strained and defective tin monosulfide/reduced graphene oxide composite demonstrates a high reversible capacity of 511.82 mAh g^(-1) at 1 A g^(-1) and an outstanding rate capability of 450.60 mAh g^(-1) at 3 A g^(-1).This study offers an effective strategy for improving sodium storage performance through lattice strain and defect engineering.
基金financially supported by the National Natural Science Foundation of China(Nos.52270149,51908528,2200013)Natural Science Foundation of Henan Province,China(No.242300421443)+1 种基金The Science and Technology Key Project of Henan Province,China(No.242102321073)Doctoral Fund Project of Henan University of Technology,China(Nos.2020BS005,2023BS004).
文摘The high band gap of zinc oxide(ZnO)has significantly limited its potential application for organic contaminant removal in photocatalysis.In this study,ZnO/halloysites(HNTs)composites(ZnO/HNTs)were prepared using a high-temperature calcination method to enhance the removal of tetracycline hydrochloride(TCH).The experimental results demonstrated that the band gap of ZnO/HNTs decreased to 3.12 eV,compared to 3.21 eV for pure ZnO.The observed removal rate(k_(obs))of TCH in the ZnO/HNTs/vis system was 1.90×10^(-2) min^(-1),significantly higher than the rates in the HNTs/vis(1.25×10^(-3)min^(-1))and ZnO/vis(1.13×10^(-2) min^(-1))systems.Additionally,ZnO/HNTs exhibited strong resistance to coexisting natural organic and inorganic matter,maintaining high pollutant removal efficiency in natural water samples.The ZnO/HNTs/vis system also effectively removed other common organic pollutants,such as ciprofloxacin and methylene blue.Cycle tests indicated that the ZnO/HNTs/vis system retained 65.57%of its original efficiency,demonstrating good reusability and versatility.Scavenging and electron paramagnetic resonance experiments identified that h+was the primary species in the ZnO/HNTs/vis system,with other species playing auxiliary roles in TCH degradation.This study provides valuable insights into the design of novel ZnO-based photocatalysts for the degradation of organic pollutants in water.
基金Project(2008BAB35B04) supported by the National Key Technology R&D Program of China
文摘Series Li-Sb-Mn composite oxides with different Sb/Mn molar ratios were obtained by solid state reaction.Their structure,morphology and Li^＋ extraction/adsorption properties were characterized by X-ray diffractometry （XRD）,scanning electron microscopy （SEM） and atomic absorption spectrophotometry （AAS）,respectively.XRD and SEM analyses reveal that the crystal of the products transfers from spinel to orthorhombic phase with the increase of molar ratio of Sb to Mn from 0.05 to 1.00.The Li^＋ extraction and adsorption experiments for these Li-Sb-Mn composite oxides demonstrate that the composite oxides can all be used as lithium inorganic adsorbents.The acid treated spinel Li-Sb-Mn composite oxide with Sb/Mn molar ratio of 0.05 has a high Li^＋ adsorption capacity of 33.23mg/g in lithium solution.The Sb/Mn molar ratio of these Li-Sb-Mn composite oxides should be a crucial factor in determining their structure and Li^＋ extraction and adsorption properties.
基金supported by the National Natural Science Foundation of China(21577088)~~
文摘The composite oxides xAg/Co_（0.93）Ce_（0.07）（x=Ag/（Co＋Ce） molar ratio）,intended for use as high performance catalytic materials,were successfully prepared via citric acid complexation.The effects of silver on the performance of these substances during soot combustion were subsequently investigated.Under O_2,the 0.3Ag/Co_（0.93）Ce_（0.07） catalyst resulted in the lowest ignition temperature,T_（10）,of197 ℃,while the minimum light-off temperature was obtained from both 0.2Ag/Co_（0.93）Ce_（0.07） and0.3Ag/Co_（0.93）Ce_（0.07） in the NO_x atmosphere.These materials were also characterized by various techniques,including H_2,soot and NO_x temperature programmed reduction,X-ray diffraction,and electron paramagnetic resonance,Raman,X-ray photoelectron,and Fourier transform infrared spectroscopic analyses.The results demonstrated that silver significantly alters the catalytic behavior under both O_2 and NO_x,even though the lattice structure of the mixed oxide is not affected.Surface silver oxides generated under the O_2 atmosphere favor soot combustion by participating in the redox cycles between soot and the silver oxide,whereas the AgNO_3 that forms in a NO_x-rich atmosphere facilitates soot abatement at a lower temperature.The inferior activity of AgNO_3 relative to that of Ag_2O results in the different catalytic performance in the presence of NO_x or O_2.
基金the State Key Fundamental Research Program(Ministry of Science and Technology of China,No.2011CBA00501)Shanghai Municipal Science and Technology Commission,China(Grant No:11DZ1200300)the Foundation of State Key Laboratory of Coal Conversion(Grant No:1112610)
文摘Cu-Fe composite oxides were prepared by co-precipitation method and tested for higher alcohol synthesis from syngas. The selectivity to C2＋OH and C6＋OH in alcohol distribution was very high while the methane product fraction in hydrocarbon distribution was rather low, demonstrating a promising potential in higher alcohols synthesis from syngas. The distribution of alcohols and hydrocarbons approximately obeyed Anderson-Schulz-Flory distribution with similar chain growth probability, indicating alcohols and hydrocarbons derived from the same intermediates. The effects of Cu/Fe molar ratio, reaction temperature and gas hourly space velocity （GHSV） on catalytic performance were studied in detail. The sample with a Cu/Fe molar ratio of 10/1 exhibited the best catalytic performance. Higher reaction temperature accelerated water-gas-shift reaction and led to lower total alcohols selectivity. GHSV showed great effect on catalytic performance and higher GHSV increased the total alcohol selectivity, indicating there existed visible dehydration reaction of alcohol into hydrocarbon.
基金supported by National Basic Research Program of China(2010CB732300,2013CB933201)National High Technology Research and Development Program of China(2011AA03A406,2012AA062703)+2 种基金the National Natural Science Foundation of China(21103048,21273150)Shu Guang Project of Shanghai Municipal Education CommissionShanghai Education Development Foundation(10SG30)
文摘Mesoporous CeO2-MnOx binary oxides with different Mn/Ce molar ratios were prepared by hydrothermal synthesis and characterized by scanning electron microscopy （SEM）, N2 sorption, X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and H2 temperature-programmed reduction （H2-TPR）. The characterization results indicated that the CeO2-MnOx catalysts exhibited flower-like microspheres with high specific surface areas, and partial Mn cations could be incorporated into CeO2 lattice to form solid solution. The CeO2-MnOx catalysts showed better catalytic activity for CO oxidation than that prepared by the coprecipitation method. Furthermore, the CeO2-MnOx catalyst with Mn/Ce molar ratio of 1 in the synthesis gel （Ce-Mn-1） exhibited the best catalytic activity, over which the conversion of CO could achieve 90% at 135 ℃. This was ascribed to presence of more Mn species with higher oxida- tion state on the surface and the better reducibility over the Ce-Mn-I catalyst than other CeO2-MnOx catalysts.
基金Project supported by National Natural Science Foundation of China(20976120)Natural Science Foundation of Tianjin(09JCYBJC06200)
文摘The nano-crystalline Cu-Ce-Zr-O composite oxides were successfully prepared by the supercritical anti-solvent （SAS） process. The physicochemical properties and catalytic performances were investigated by X-ray diffraction （XRD）, Raman spectroscopy, H2 temperature-programmed reduction （H2 -TPR）, oxygen storage capacity （OSC） measurement and catalytic activity evaluation. It was found that Cu2＋ ions incorporated into CeO2 -ZrO2 lattice to form Cu-Ce-Zr-O solid solution associated with the formation of oxygen vacancies. The Cu-Ce-Zr-O catalysts prepared via the SAS process with the Cu content 2.63 mol.% showed the highest OSC index of 636.9 μmol/g. Compared with the samples prepared by impregnation method, Cu doping using SAS process could improve the dispersion of Cu2＋ in the composite oxide, enhance the interaction between Cu2＋ and CeO2-ZrO2 , improve the reducibility of catalyst, and thus improve the OSC performance and increase the catalytic activity for CO oxidation at low temperature.
基金financially supported by the National Natural Science Foundation of China (No. 51404034)
文摘The hydrogen permeation resistance of Si–Zr(SZ) and Si–Al(SA) composite sol oxide coating on zirconium hydride blocks(Zr H) was studied. SZ and SA composite sol were prepared by sol–gel method. SZ and SA composite oxide coatings were prepared on the surface of Zr H(in situ oxidized or not) in turns by dip-coating and heat treatment. Hydrogen permeation of Zr Hwith and without composite oxide coating was compared.Hydrogen desorption experiments in thermal vacuum show that hydrogen permeation resistance of SA composite oxide coating is better than that of SZ, to a certain extent,which could decrease hydrogen thermal loss. Experimental results in the working condition show that the SA composite oxide coating can not only prevent hydrogen permeation, but also retard contact and reaction between COand Zr Hmatrix, which could mitigate excessive oxidation of in situ oxide film. Differential scanning calorimetry and thermogravimetry(DSC–TG) analysis was performed to investigate the decomposition behavior of SA and SZ liquid sol in heat treatment process. X-ray diffraction(XRD) and scanning electron microscopy(SEM) analysis were employed to characterize the phase composition,surface and cross-section morphology of the coatings.
基金Project supports from National Nature Science Foundation of China(21177110)
文摘HZSM-5, Al_2O_3, TiO_2 and SiO_2 supported CeO_2-ZrO_2-CrO_x catalysts were prepared by deposition-precipitation method and tested for deep catalytic oxidation of 1,2-dichloroethane（DCE）, as one of the common chlorinated organic pollutants. All the catalysts were characterized by means of N_2 adsorption-desorption, X-ray photoelectron spectroscopy（XPS）, ammonia-temperatureprogrammed desorption（NH_3-TPD） and hydrogen temperature-programmed reduction（H2-TPR）. The characterization results revealed that there was strongly synergistic effect between the oxidizability of CZCr species and the acidity of supports, which obviously promoted the catalytic activity for DCE degradation. 20% CZCr/HZSM-5 showed the highest activity and good durability during the long-term continuous test. The catalytic activity decreased in the order： 20%CZCr/HZSM-5〉CZCr〉20%CZCr/TiO_2〉20%CZCr/Al_2O_3〉20%CZCr/SiO_2.
基金Supported by National Natural Science Foundation of China(Nos.50378004 and 50678007)Beijing Natural Science Foun-dation(No.8082009)+1 种基金Science & Technology Development Programme of Beijing Municipal Commission of Education (No.KM200610005025)Academic Human Resources Development in Institutions of Higher Learning Under the Jurisdiction of Beijing Municipality(No. 05004014200701).
文摘Iron-manganese composited oxide（FeMnO） was prepared with potassium permanganate and ferrous salt. Interface performance, charge property and structure topography of the FeMnO were investigated. Coagulation efficiency and pollution removal mechanism of the FeMnO were approached. Results show that the main compositions of the FeMnO are δ-manganese dioxide and ferric hydroxide. The specific surface area is about 146.22 m^2/g. The FeMnO contains rich hydroxyl with extremely strong adsorption action and chemical adsorption activity. The zero charge point of the oxide in pure water is about 8.0 of pH value. Under neutral pH value conditions, the FeMnO particle surface carried positive charges. The FeMnO particles are quasi-spherical micro-particles with irregular sizes adjoined each other to form net construction. Phosphorus removal efficiency of the FeMnO is remarkable, the total dissoluble phosphorus of settled water can be reduced below detecting level（0.3 μtg/L） at a FeMnO dosage of 6 mg/L, and total phosphorus below detecting level at a FeMnO dosage of 10 mg/L, for water samples containing total phos- phorus of 1281.70 μg/L and total dissoluble phosphorus of 1187.91 μtg/L. The mechanism of effective coagulation for phosphorus removal is combined results of multiple actions of adsorption, charge neutralization, adsorption/bridging and so on.
