ZrO2/TiO2 composite photocatalytic film was produced on the pure titanium substrate using in-situ Zr(OH)4 colloidal particle by the micro-arc oxidation technique and characterized by scanning electron microscope (...ZrO2/TiO2 composite photocatalytic film was produced on the pure titanium substrate using in-situ Zr(OH)4 colloidal particle by the micro-arc oxidation technique and characterized by scanning electron microscope (SEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD) and ultraviolet-visible (UV-Vis) spectrophotometer. The composite film shows a lamellar and porous structure which consists of anatase, futile and ZrO2 phases. The optical absorption edge of film is shifted to longer wavelength when ZrO2 is introduced to TiO2. Furthermore, the photocatalytic reaction rate constants of degradation of rhodamine B solution with ZrO2/TiO2 composite film and pure TiO2 film under ultraviolet irradiation are measured as 0.0442 and 0.0186 h 1, respectively.展开更多
Au-Pt/SnO2/GC composite electrode was prepared by self-assembling Au-Pt nanoparticles on SnO2 film,which was deposited on actived glassy carbon(GC).Atomic force microscopy(AFM)and scanning electron microscopy(SEM)imag...Au-Pt/SnO2/GC composite electrode was prepared by self-assembling Au-Pt nanoparticles on SnO2 film,which was deposited on actived glassy carbon(GC).Atomic force microscopy(AFM)and scanning electron microscopy(SEM)images revealed that dense and uniform Au-Pt particles with 25-nm diameter were dispersed on SnO2 film.X-ray photoelectron spectroscopy(XPS)results proved that there was an interaction between Au-Pt nanoparticles and SnO2 support.Electrochemical experiments showed that Au-Pt/SnOz/GC composite electrode had a good electrocatalytic activity to the oxidation of methanol.展开更多
PEO-LiClO4-TiO2 composite polymer electrolyte films were prepared. TiO2 was formed directly in matrix by hydrolysis and condensation reaction of tetrabutyl titanate. The crystallinity, morphology and ionic conductivit...PEO-LiClO4-TiO2 composite polymer electrolyte films were prepared. TiO2 was formed directly in matrix by hydrolysis and condensation reaction of tetrabutyl titanate. The crystallinity, morphology and ionic conductivity of composite polymer electrolyte films were examined by differential scanning calorimetry, scanning electron microscopy, atom force microscopy and alternating current impedance spectroscopy, respectively. The glass transition temperature and the crystallinity of composite polymer electrolytes are decreased compared with those of PEO-LiClO4 polymer electrolyte film. The results show that TiO2 particles are uniformly dispersed in PEO-LiClO4-5%TiO2 composite polymer electrolyte film. The maximal conductivity of 5.5×10、5 Scm at 20 ℃ of PEO-LiClO4-TiO2 film is obtained at 5% mass fraction of TiO2.展开更多
[Zn(CH3COO)2 + PVP]/[C2H5O)4Si + PVP]/[SnCl4 + PVP]/[Ti(OC4H9)4 + CH3COOH + PVP] precursor composite fibers have been fabricated through self-made electrospinning equipment via electrospinning tech-nique. ZnO/SiO2/SnO...[Zn(CH3COO)2 + PVP]/[C2H5O)4Si + PVP]/[SnCl4 + PVP]/[Ti(OC4H9)4 + CH3COOH + PVP] precursor composite fibers have been fabricated through self-made electrospinning equipment via electrospinning tech-nique. ZnO/SiO2/SnO2/TiO2 composite nanofibers were obtained by calcination of the relevant precursor composite fibers. The samples were characterized by thermogravimetric-differential thermal analysis (TG-DTA), X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), and Scanning electron microscopy (SEM). TG-DTA analysis reveals that solvents, organic compounds and inorganic in the precursor composite fibers are decomposed and volatilized totally, and the mass of the samples kept constant when sintering temperature was above 900?C, and the total mass loss percentage is 88%. XRD results show that the precursor composite fibers are amorphous in structure, and pure phase ZnO/SiO2/SnO2/TiO2 com-posite nanofibers are obtained by calcination of the relevant precursor composite fibers. FTIR analysis manifests that pure inorganic oxides are formed. SEM analysis indicates that the width of the precursor composite fibers is ca. 1.485 ± 0.043 μm. The width of the ZnO/SiO2/SnO2/TiO2 composite nanofibers is ca. 1145.098 ± 68.093 nm.展开更多
Al2O3 ceramic powder was applied to modify the large pores defects on the surface of the porous metal Ti support,in situ oxidation method was a convenient method to prepare defect free ceramic/Ti composite membranes o...Al2O3 ceramic powder was applied to modify the large pores defects on the surface of the porous metal Ti support,in situ oxidation method was a convenient method to prepare defect free ceramic/Ti composite membranes on this basis.In situ oxidation conditions experimental results show that the best condition for preparing the TiO2-Al2O3/Ti composite membrane is under 800°C for 2 h,and the microstructure and pore sizes of the TiO2-Al2O3/Ti composite membranes are affected obviously.The thickness and composition of the TiO2/Ti composite membranes are determined by SEM and XRD completely.The pore size distribution of the composite membrane is measured by bubble pressure method,the most probable aperture is about 3.12μm,while the average pore size of defect free TiO2-Al2O3/Ti is about 3.23μm.After ultrasonic treatment,the slight weight change of membranes reveals no observable change,which indicates that TiO2-Al2O3/Ti composite membranes maintain a good stability.展开更多
This research work aims to reduce the band gap of thin layers of titanium oxide by the incorporation of graphene oxide sheets. Thin layers of the TiO2-GO composites were prepared on a glass substrate by the spin-coati...This research work aims to reduce the band gap of thin layers of titanium oxide by the incorporation of graphene oxide sheets. Thin layers of the TiO2-GO composites were prepared on a glass substrate by the spin-coating technique from GO and an aqueous solution of TiO2. A significant decrease in optical band gap was observed at the TiO2-GO compound compared to that of pure TiO2. Samples as prepared were characterized using XRD, SEM and UV-visible spectra. XRD analysis revealed the amorphous nature of the deposited layers. Scanning electron microscope reveals the dispersion of graphene nanofiles among titanium oxide nanoparticles distributed at the surface with an almost uniform size distribution. The band gap has been calculated and is around 2 eV after incorporation of Graphene oxide. The chemical bond C-Ti between the titanium oxide and graphene sheets is at the origin of this reduction.展开更多
The conductivities of polyethylene oxide (PEO)-based polymer electrolytes (PE) can be improved by the addition of inorganic inert powder. The composite polymer electrolytes (CPE) PEO10LiX (X=4ClO- or 322N(CFSO)-)-Li2T...The conductivities of polyethylene oxide (PEO)-based polymer electrolytes (PE) can be improved by the addition of inorganic inert powder. The composite polymer electrolytes (CPE) PEO10LiX (X=4ClO- or 322N(CFSO)-)-Li2TiO3 were prepared by solution casting with inorganic solid electrolyte Li2TiO3 powder as a filler. Results showed that the conductivities of PEO10LiClO4-3wt% Li2TiO3 and PEO10LiN(CF3SO2)2-10wt% Li2TiO3 at 30 ℃ were 8.6×10-6 and 5.6×10-5 S·cm-1, respectively. The conductivities of CPE increased with the decrease of filler抯 particle size. The ionic conduction mechanism analysis showed that there may be three conduction routes in the CPE, i.e., PEO bulk, polymer-filler interface and Li2TiO3 crystal.展开更多
Pd supported on TiO2-Al2O3 binary oxides prepared by coprecipitation method has been investigated for the total oxidation of methane. All Pd/TiO2-Al2O3 catalysts show higher activity than Pd/Al2O3 and Pd/TiO2. Among t...Pd supported on TiO2-Al2O3 binary oxides prepared by coprecipitation method has been investigated for the total oxidation of methane. All Pd/TiO2-Al2O3 catalysts show higher activity than Pd/Al2O3 and Pd/TiO2. Among them, Pd/2Ti-3Al with a Ti/Al ratio of 2 to 3 has a T90% of 395 ℃ at a gas hourly mass velocity of 33000 mL/(h*g), which is at least 50 ℃ lower than that of Pd supported on single metal oxide Al2O3 or TiO2. The results of TPR and ^180-isotope exchange experiments demonstrated that the excellent activity of Pd/2Ti-3Al was due to its high oxygen mobility and moderate reducibility, which is in accordance with our previous work, XPS results indicated that the dispersion of Pd was not the key factor to influence the catalytic activity.展开更多
基金Project(gf200901002)supported by the Open Research Fund of National Defense Key Disciplines Laboratory of Light Alloy Processing Science and Technology of Nanchang Hangkong University,China
摘要ZrO2/TiO2 composite photocatalytic film was produced on the pure titanium substrate using in-situ Zr(OH)4 colloidal particle by the micro-arc oxidation technique and characterized by scanning electron microscope (SEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD) and ultraviolet-visible (UV-Vis) spectrophotometer. The composite film shows a lamellar and porous structure which consists of anatase, futile and ZrO2 phases. The optical absorption edge of film is shifted to longer wavelength when ZrO2 is introduced to TiO2. Furthermore, the photocatalytic reaction rate constants of degradation of rhodamine B solution with ZrO2/TiO2 composite film and pure TiO2 film under ultraviolet irradiation are measured as 0.0442 and 0.0186 h 1, respectively.
基金supported by the High-Tech Research and Development Program of China(No.2007AA03Z219)the Funding Project for Academic Human Resources Development in Institutions of Higher Learning under the Jurisdiction of Beijing Municipality,and the Beijing Natural Science Foundation(No.207001)
摘要Au-Pt/SnO2/GC composite electrode was prepared by self-assembling Au-Pt nanoparticles on SnO2 film,which was deposited on actived glassy carbon(GC).Atomic force microscopy(AFM)and scanning electron microscopy(SEM)images revealed that dense and uniform Au-Pt particles with 25-nm diameter were dispersed on SnO2 film.X-ray photoelectron spectroscopy(XPS)results proved that there was an interaction between Au-Pt nanoparticles and SnO2 support.Electrochemical experiments showed that Au-Pt/SnOz/GC composite electrode had a good electrocatalytic activity to the oxidation of methanol.
摘要PEO-LiClO4-TiO2 composite polymer electrolyte films were prepared. TiO2 was formed directly in matrix by hydrolysis and condensation reaction of tetrabutyl titanate. The crystallinity, morphology and ionic conductivity of composite polymer electrolyte films were examined by differential scanning calorimetry, scanning electron microscopy, atom force microscopy and alternating current impedance spectroscopy, respectively. The glass transition temperature and the crystallinity of composite polymer electrolytes are decreased compared with those of PEO-LiClO4 polymer electrolyte film. The results show that TiO2 particles are uniformly dispersed in PEO-LiClO4-5%TiO2 composite polymer electrolyte film. The maximal conductivity of 5.5×10、5 Scm at 20 ℃ of PEO-LiClO4-TiO2 film is obtained at 5% mass fraction of TiO2.
摘要[Zn(CH3COO)2 + PVP]/[C2H5O)4Si + PVP]/[SnCl4 + PVP]/[Ti(OC4H9)4 + CH3COOH + PVP] precursor composite fibers have been fabricated through self-made electrospinning equipment via electrospinning tech-nique. ZnO/SiO2/SnO2/TiO2 composite nanofibers were obtained by calcination of the relevant precursor composite fibers. The samples were characterized by thermogravimetric-differential thermal analysis (TG-DTA), X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), and Scanning electron microscopy (SEM). TG-DTA analysis reveals that solvents, organic compounds and inorganic in the precursor composite fibers are decomposed and volatilized totally, and the mass of the samples kept constant when sintering temperature was above 900?C, and the total mass loss percentage is 88%. XRD results show that the precursor composite fibers are amorphous in structure, and pure phase ZnO/SiO2/SnO2/TiO2 com-posite nanofibers are obtained by calcination of the relevant precursor composite fibers. FTIR analysis manifests that pure inorganic oxides are formed. SEM analysis indicates that the width of the precursor composite fibers is ca. 1.485 ± 0.043 μm. The width of the ZnO/SiO2/SnO2/TiO2 composite nanofibers is ca. 1145.098 ± 68.093 nm.
基金Projects(212006065,21666018)supported by the National Natural Science Foundation of China
摘要Al2O3 ceramic powder was applied to modify the large pores defects on the surface of the porous metal Ti support,in situ oxidation method was a convenient method to prepare defect free ceramic/Ti composite membranes on this basis.In situ oxidation conditions experimental results show that the best condition for preparing the TiO2-Al2O3/Ti composite membrane is under 800°C for 2 h,and the microstructure and pore sizes of the TiO2-Al2O3/Ti composite membranes are affected obviously.The thickness and composition of the TiO2/Ti composite membranes are determined by SEM and XRD completely.The pore size distribution of the composite membrane is measured by bubble pressure method,the most probable aperture is about 3.12μm,while the average pore size of defect free TiO2-Al2O3/Ti is about 3.23μm.After ultrasonic treatment,the slight weight change of membranes reveals no observable change,which indicates that TiO2-Al2O3/Ti composite membranes maintain a good stability.
摘要This research work aims to reduce the band gap of thin layers of titanium oxide by the incorporation of graphene oxide sheets. Thin layers of the TiO2-GO composites were prepared on a glass substrate by the spin-coating technique from GO and an aqueous solution of TiO2. A significant decrease in optical band gap was observed at the TiO2-GO compound compared to that of pure TiO2. Samples as prepared were characterized using XRD, SEM and UV-visible spectra. XRD analysis revealed the amorphous nature of the deposited layers. Scanning electron microscope reveals the dispersion of graphene nanofiles among titanium oxide nanoparticles distributed at the surface with an almost uniform size distribution. The band gap has been calculated and is around 2 eV after incorporation of Graphene oxide. The chemical bond C-Ti between the titanium oxide and graphene sheets is at the origin of this reduction.
摘要The conductivities of polyethylene oxide (PEO)-based polymer electrolytes (PE) can be improved by the addition of inorganic inert powder. The composite polymer electrolytes (CPE) PEO10LiX (X=4ClO- or 322N(CFSO)-)-Li2TiO3 were prepared by solution casting with inorganic solid electrolyte Li2TiO3 powder as a filler. Results showed that the conductivities of PEO10LiClO4-3wt% Li2TiO3 and PEO10LiN(CF3SO2)2-10wt% Li2TiO3 at 30 ℃ were 8.6×10-6 and 5.6×10-5 S·cm-1, respectively. The conductivities of CPE increased with the decrease of filler抯 particle size. The ionic conduction mechanism analysis showed that there may be three conduction routes in the CPE, i.e., PEO bulk, polymer-filler interface and Li2TiO3 crystal.
基金Project supported by the Major State Basic Research Development Program (No. G2000077503), the National Natural Science Foundation of China (No. 20173002), and Cooperation Project between NSFC and DFG (No. 20411130104).
摘要Pd supported on TiO2-Al2O3 binary oxides prepared by coprecipitation method has been investigated for the total oxidation of methane. All Pd/TiO2-Al2O3 catalysts show higher activity than Pd/Al2O3 and Pd/TiO2. Among them, Pd/2Ti-3Al with a Ti/Al ratio of 2 to 3 has a T90% of 395 ℃ at a gas hourly mass velocity of 33000 mL/(h*g), which is at least 50 ℃ lower than that of Pd supported on single metal oxide Al2O3 or TiO2. The results of TPR and ^180-isotope exchange experiments demonstrated that the excellent activity of Pd/2Ti-3Al was due to its high oxygen mobility and moderate reducibility, which is in accordance with our previous work, XPS results indicated that the dispersion of Pd was not the key factor to influence the catalytic activity.