TiO2-SnO2-SiO2 nanocomposite photocatalysts were prepared with Na2SiO3·9H2O, SnCl4·5H2O and TiCl4 as precursors by chemistry coating processes and supercritical fluid drying (SCFD) method. Characterizations ...TiO2-SnO2-SiO2 nanocomposite photocatalysts were prepared with Na2SiO3·9H2O, SnCl4·5H2O and TiCl4 as precursors by chemistry coating processes and supercritical fluid drying (SCFD) method. Characterizations with XRD, TEM, NMR and FTIR showed that in addition to anatase type TiO2, a new active phase(Ti,Sn)O2 was also formed in the range of the studied doping concentration, The catalytic activity was evaluated by photocatalytic degradation of phenol as model reaction. SiO2 remained amphorous at all samples. It could prevent from growth of the size of nanopaticle and transformation from anatase to rutile. Compared with pure TiO2, or TiO2-SnO2 catalyst prepared by Sol-gel method, Nano-composite photo-catalyst showed significant improvement in catalytic activity, the photo-catalytic degradation rate of phenol in 7 h reached 88.7%. Application of the composite catalysts for the photocatalytic decomposition of phenol not only gave the same activity relative to pure ultrafine TiO2, but also reduced cost. The experimental results also proved that the thermal stability of TiO2 was greatly enhanced after mixing with small amount of SiO2. The optimized doping of SiO2 was 20.3%. The photo-catalyst prepared by SCFD combination technology was characterized with smaller particle size, larger surface area and higher activity.展开更多
Compound Zn2Sn0.8Ti0.2O4 was synthesized by a hydrothermal method in which SnCl4-5H2O,TiCl4,ZnCl2 and N2H4-H2O were used as reactants.The composite Zn2Sn0.8Ti0.2O4/C was then prepared through a carbothermic reduction ...Compound Zn2Sn0.8Ti0.2O4 was synthesized by a hydrothermal method in which SnCl4-5H2O,TiCl4,ZnCl2 and N2H4-H2O were used as reactants.The composite Zn2Sn0.8Ti0.2O4/C was then prepared through a carbothermic reduction process using the as-prepared Zn2Sn0.8Ti0.2O4 and glucose as reactants.The structure,morphology and electrochemical properties of the as-prepared products were investigated by XRD,XPS,TEM and electrochemical measurements.In addition,electrochemical Li insertion/extraction in composite Zn2Sn0.8Ti0.2O4/C were examined by ex situ XRD and SEM.The first discharge capacity of Zn2SnO4 is about 1670.8 mA-h/g,with a capacity retain of 342.7 mA-h/g in the 40th cycle at a constant current density of 100 mA/g in the voltage range of 0.05-3.0 V.Comparing with the Zn2SnO4,some improved electrochemical properties are obtained for Zn2Sn0.8Ti0.2O4,Zn2SnO4/C and Zn2Sn0.8Ti0.2O4/C.The composite Zn2Sn0.8Ti0.2O4/C shows the best electrochemical properties,and its first discharge capacity is about 1530.0 mA-h/g,with a capacity retain of 479.1 mA-h/g the 100th cycle.展开更多
采用溶胶-凝胶法制备Ti/Sn O_2-F电极,进行全氟辛酸(PFOA)电氧化降解的研究,实验考察了F替代Sb掺杂、电流密度、初始pH值和支持电解质对PFOA降解效率的影响。结果表明,当F替代Sb掺杂Sn O_2,电流密度为20 m A/cm^2,初始pH值3.7,支持电解...采用溶胶-凝胶法制备Ti/Sn O_2-F电极,进行全氟辛酸(PFOA)电氧化降解的研究,实验考察了F替代Sb掺杂、电流密度、初始pH值和支持电解质对PFOA降解效率的影响。结果表明,当F替代Sb掺杂Sn O_2,电流密度为20 m A/cm^2,初始pH值3.7,支持电解质为NaClO_4时,电解30 min后PFOA的降解率达98%。采用液相色谱-质谱联用(HPLC-MS/MS)和离子色谱(IC)对PFOA降解产物进行分析,解析了PFOA电氧化降解的反应机理。展开更多
A series of TiO2-SnO2 nano-sized composite photo-catalysts containing Sn (9.3%-30.1%) were prepared from TiCI4 and SnCl4·5H2O by using sol-gel, supercritical fluid dry and solid-phase reaction (SCFD) combination ...A series of TiO2-SnO2 nano-sized composite photo-catalysts containing Sn (9.3%-30.1%) were prepared from TiCI4 and SnCl4·5H2O by using sol-gel, supercritical fluid dry and solid-phase reaction (SCFD) combination technology. Characterizations with X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier Transform Infrared Spectroscopy (FTIR) showed that, in addition to anatase type TiO2, a new active phase (Ti, Sn)O2 (with particle size of 2.0-4.3 nm) formed, and there were no SnO2 crystals observed in the range of the doping concentration studied. Photo-catalytic reaction of phenol was used as a model reaction to evaluate the catalytic activities of the obtained catalysts. Compared with pure TiO2 or Ti-Sn catalyst prepared with general sol-gel method, Ti-Sn nano-composite photo-catalyst thus obtained showed significant improvement in catalytic activity. The photo-catalytic degradation rate of phenol could reach as high as 93.5% after 7 h. The preparation conditions of the new phase (Ti, Sn)O2 were investigated and its catalytic mechanism was proposed. The photo-catalytic particles prepared using SCFD combination technology exhibited small particle size, large surface area and high activity.展开更多
The electrochemical oxidation of chlorimuron-ethyl on metry. The electrochemical behaviour of the electrode in a sodium Ti/SnO2-Sb2O5/PbO2 electrode was studied by cyclic voltamsulfate solution and in the mixture solu...The electrochemical oxidation of chlorimuron-ethyl on metry. The electrochemical behaviour of the electrode in a sodium Ti/SnO2-Sb2O5/PbO2 electrode was studied by cyclic voltamsulfate solution and in the mixture solution of sodium sulfate and chlorimuron-ethyl was studied. The experimental results of cyclic voltammetry show that the acidic medium was suitable for the efficient electrochemical oxidation of chlorimuron-ethyl. Some electro-generated reagent was formed in the electrolysis process and chlorimuron-ethyl could be oxidized by the electro-generated reagent. A Ti/SnO2-Sb2O5/PbO2 electrode was used as the anode and the electrolysis experiment was carried out under the optimized conditions. The electrolysis process was monitored by UV-Vis spectrometry and high performance liquid chromatography（HPLC）, and the chemical oxygen demand（COD） was determined by the potassium dichromate method. The mechanism of chlorimuron-ethyl to be oxided was studied primarily by the cyclic voltammetry and UV-Vis spectrometry. The results of electrolysis experiment demonstrate the possibility of the electrode to be used as an anode for the electrochemical treatment of chlorimuron-ethyl contained in waste water.展开更多
The humidity sensing properties of La^3＋ and K^＋ co-doped Ti0.9Sn0.1O2 thin films were investigated. The humidity sensitive thin films were prepared by sol-gel method on alumina substrates. The sensing behaviors of ...The humidity sensing properties of La^3＋ and K^＋ co-doped Ti0.9Sn0.1O2 thin films were investigated. The humidity sensitive thin films were prepared by sol-gel method on alumina substrates. The sensing behaviors of thin films were inspected at different sintering temperatures by constructing a humidity-impedance measuring system. It was found that the addition of rare earth ion La^3＋ and alkali ion K^＋ was beneficial for improving the humidity sensitive properties of the samples and La0.003K0.5Ti0.9Sn0.1O2 sintered at 500 ℃ for 4 h showed the best humidity sensing properties. The impedance of this thin film decreased from 109 to 104 Ω with excellent linearity in the humidity range of 11%-95%. Narrow hysteresis loop, prominent stability and high sensitivity were obtained. The effects of dopant con-tent and doping mechanism on humidity sensitivity were also discussed in terms of segregation of rare earth ions at grain boundaries and granularity of crystalline and influence of K^＋ on the decrease in the intrinsic resistance of the materials, and increase in the number of wa-ter adsorption sites.展开更多
文摘TiO2-SnO2-SiO2 nanocomposite photocatalysts were prepared with Na2SiO3·9H2O, SnCl4·5H2O and TiCl4 as precursors by chemistry coating processes and supercritical fluid drying (SCFD) method. Characterizations with XRD, TEM, NMR and FTIR showed that in addition to anatase type TiO2, a new active phase(Ti,Sn)O2 was also formed in the range of the studied doping concentration, The catalytic activity was evaluated by photocatalytic degradation of phenol as model reaction. SiO2 remained amphorous at all samples. It could prevent from growth of the size of nanopaticle and transformation from anatase to rutile. Compared with pure TiO2, or TiO2-SnO2 catalyst prepared by Sol-gel method, Nano-composite photo-catalyst showed significant improvement in catalytic activity, the photo-catalytic degradation rate of phenol in 7 h reached 88.7%. Application of the composite catalysts for the photocatalytic decomposition of phenol not only gave the same activity relative to pure ultrafine TiO2, but also reduced cost. The experimental results also proved that the thermal stability of TiO2 was greatly enhanced after mixing with small amount of SiO2. The optimized doping of SiO2 was 20.3%. The photo-catalyst prepared by SCFD combination technology was characterized with smaller particle size, larger surface area and higher activity.
基金Project (51004028) supported by the National Natural Science Foundation of China
文摘Compound Zn2Sn0.8Ti0.2O4 was synthesized by a hydrothermal method in which SnCl4-5H2O,TiCl4,ZnCl2 and N2H4-H2O were used as reactants.The composite Zn2Sn0.8Ti0.2O4/C was then prepared through a carbothermic reduction process using the as-prepared Zn2Sn0.8Ti0.2O4 and glucose as reactants.The structure,morphology and electrochemical properties of the as-prepared products were investigated by XRD,XPS,TEM and electrochemical measurements.In addition,electrochemical Li insertion/extraction in composite Zn2Sn0.8Ti0.2O4/C were examined by ex situ XRD and SEM.The first discharge capacity of Zn2SnO4 is about 1670.8 mA-h/g,with a capacity retain of 342.7 mA-h/g in the 40th cycle at a constant current density of 100 mA/g in the voltage range of 0.05-3.0 V.Comparing with the Zn2SnO4,some improved electrochemical properties are obtained for Zn2Sn0.8Ti0.2O4,Zn2SnO4/C and Zn2Sn0.8Ti0.2O4/C.The composite Zn2Sn0.8Ti0.2O4/C shows the best electrochemical properties,and its first discharge capacity is about 1530.0 mA-h/g,with a capacity retain of 479.1 mA-h/g the 100th cycle.
基金The authors thank the National Natural Scir nce Foun-dation of China(No.20076004)the National Development Project of High Technology(No.2001AA322030)the Doctoral Program of Higher Education(No.2000001005)for the financial support of this project.
文摘A series of TiO2-SnO2 nano-sized composite photo-catalysts containing Sn (9.3%-30.1%) were prepared from TiCI4 and SnCl4·5H2O by using sol-gel, supercritical fluid dry and solid-phase reaction (SCFD) combination technology. Characterizations with X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier Transform Infrared Spectroscopy (FTIR) showed that, in addition to anatase type TiO2, a new active phase (Ti, Sn)O2 (with particle size of 2.0-4.3 nm) formed, and there were no SnO2 crystals observed in the range of the doping concentration studied. Photo-catalytic reaction of phenol was used as a model reaction to evaluate the catalytic activities of the obtained catalysts. Compared with pure TiO2 or Ti-Sn catalyst prepared with general sol-gel method, Ti-Sn nano-composite photo-catalyst thus obtained showed significant improvement in catalytic activity. The photo-catalytic degradation rate of phenol could reach as high as 93.5% after 7 h. The preparation conditions of the new phase (Ti, Sn)O2 were investigated and its catalytic mechanism was proposed. The photo-catalytic particles prepared using SCFD combination technology exhibited small particle size, large surface area and high activity.
基金Supported by the Science and Technology Foundation of the Education Department of Liaoning Province,China (No.2009A557)
文摘The electrochemical oxidation of chlorimuron-ethyl on metry. The electrochemical behaviour of the electrode in a sodium Ti/SnO2-Sb2O5/PbO2 electrode was studied by cyclic voltamsulfate solution and in the mixture solution of sodium sulfate and chlorimuron-ethyl was studied. The experimental results of cyclic voltammetry show that the acidic medium was suitable for the efficient electrochemical oxidation of chlorimuron-ethyl. Some electro-generated reagent was formed in the electrolysis process and chlorimuron-ethyl could be oxidized by the electro-generated reagent. A Ti/SnO2-Sb2O5/PbO2 electrode was used as the anode and the electrolysis experiment was carried out under the optimized conditions. The electrolysis process was monitored by UV-Vis spectrometry and high performance liquid chromatography（HPLC）, and the chemical oxygen demand（COD） was determined by the potassium dichromate method. The mechanism of chlorimuron-ethyl to be oxided was studied primarily by the cyclic voltammetry and UV-Vis spectrometry. The results of electrolysis experiment demonstrate the possibility of the electrode to be used as an anode for the electrochemical treatment of chlorimuron-ethyl contained in waste water.
文摘The humidity sensing properties of La^3＋ and K^＋ co-doped Ti0.9Sn0.1O2 thin films were investigated. The humidity sensitive thin films were prepared by sol-gel method on alumina substrates. The sensing behaviors of thin films were inspected at different sintering temperatures by constructing a humidity-impedance measuring system. It was found that the addition of rare earth ion La^3＋ and alkali ion K^＋ was beneficial for improving the humidity sensitive properties of the samples and La0.003K0.5Ti0.9Sn0.1O2 sintered at 500 ℃ for 4 h showed the best humidity sensing properties. The impedance of this thin film decreased from 109 to 104 Ω with excellent linearity in the humidity range of 11%-95%. Narrow hysteresis loop, prominent stability and high sensitivity were obtained. The effects of dopant con-tent and doping mechanism on humidity sensitivity were also discussed in terms of segregation of rare earth ions at grain boundaries and granularity of crystalline and influence of K^＋ on the decrease in the intrinsic resistance of the materials, and increase in the number of wa-ter adsorption sites.
