Bismuth-doped tin dioxide nanometer powders were prepared by co-precipitation method using SnCl4 and Bi（NO3）3 as raw materials. The effects of calcining temperature and doping ratio on the particle size, composition...Bismuth-doped tin dioxide nanometer powders were prepared by co-precipitation method using SnCl4 and Bi（NO3）3 as raw materials. The effects of calcining temperature and doping ratio on the particle size, composition, spectrum selectivity of bismuth-doped tin dioxide and the phase transition of Bi-Sn precursor at different temperatures were studied by means of X-ray diffraction, transmission electron microscopy, ultraviolet-visual-near infrared diffuse reflection spectrum and the thermogravimetric-differential scanning calorimetry. The results show that prepared bismuth-doped tin dioxide powders have excellent characteristics with a single-phase tetragonal structure, good dispersibility, good absorbency for ultraviolet ray and average particle size less than 10 nm. The optimum conditions for preparing bismuth-doped tin dioxide nanometer powders are as follows: calcining temperature of 600℃, ratio of bismuth-doped in a range of 0.10-0.30, and Bi-Sn precursor being dispersed by ultrasonic wave and refluxed azeotropic and distillated with mixture of n-butanol and benzene. The mechanism of phase transition of Bi-Sn precursor is that Bi 3+ enters Sn-vacancy and then forms Sn—O—Bi bond.展开更多
The precursors with NiCO3·2Ni（OH）2·2H2O, Fe2O3·nH2O coated alumina microspheres were prepared by the aqueous heterogeneous precipitation using metal salts, ammonium bicarbonate and α-Al2O3 micropowde...The precursors with NiCO3·2Ni（OH）2·2H2O, Fe2O3·nH2O coated alumina microspheres were prepared by the aqueous heterogeneous precipitation using metal salts, ammonium bicarbonate and α-Al2O3 micropowders as the starting materials. Magnetic metal Ni, α-Fe coated alumina, core-shell structural microspheres were successfully obtained by thermal reduction of the precursors at 700℃ for 2h, respectively. Powders of the precursors and the resultant metal （Ni, α-Fe） coated alumina micropowders were characterized by scanning electron microscopy, energy dispersive spectroscopy and X-ray diffraction. The results show that optimized precipitation parameters are concentration of alumina micropowders of 15g/L, rate of adding reactants of 5mL/min and pH value of 7.5. And under the optimized conditions, the spherical precursors without aggregations or agglomerations are obtained, then transferred into Ni, α-Fe coated alumina microspheres by thermal reduction. It is possible to adjust metal coating thicknesses and fabricate a multilayer structured metal/ceramics, core-shell microspherical powder materials.展开更多
Proper utilization of the FeSO4·7H2O waste slag generated from TiO2 industry is an urgent need, and Fe3O4 particles are currently being widely used in the wastewater flocculation field. In this work, magnetite wa...Proper utilization of the FeSO4·7H2O waste slag generated from TiO2 industry is an urgent need, and Fe3O4 particles are currently being widely used in the wastewater flocculation field. In this work, magnetite was recovered from ferrous sulphate by a novel co-precipitation method with calcium hydroxide as the precipitant. Under optimum conditions, the obtained spherical magnetite particles are well crystallized with a Fe304 purity of 88.78%, but apt to aggregate with a median particle size of 1.83 μm. Magnetic measurement reveals the obtained Fe304 particles are soft magnetic with a saturation magnetization of 81.73 A-m2/kg. In addition, a highly crystallized gypsum co-product is obtained in blocky or irregular shape. Predictably, this study would provide additional opportunities for future application of low-cost Fe3O4 particles in water treatment field.展开更多
The solid sodium hydroxide neutralized acidic As-containing wastewater till pH value was 6. Green copper arsenite was prepared after copper sulfate was added into the neutralized wastewater when the molar ratio of Cu ...The solid sodium hydroxide neutralized acidic As-containing wastewater till pH value was 6. Green copper arsenite was prepared after copper sulfate was added into the neutralized wastewater when the molar ratio of Cu to As was 2：1 and pH value of the neutralized wastewater was adjusted to 8.0 by sodium hydroxide. The arsenious acid solution and red residue were produced after copper arsenite mixed with water according to the ratio of liquid to solid of 4：1 and copper arsenite was reduced by SO2 at 60℃ for 1 h. The white powder was gained after the arsenious acid solution was evaporated and cooled. Copper sulfate solution was obtained after the red residue was leached by H2SO4 solution under the action of air. The results show that red residue is Cu3（SO3）2·2H2O and the white powder is As2O3. The leaching rate of Cu reaches 99.00% when the leaching time is 1.5 h, molar ratio of H2SO4 to Cu is 1.70, H2SO4 concentration is 24% and the leaching temperature is 80 ℃. The direct recovery rate of copper sulfate is 79.11% and the content of CuSOa·5H2O is up to 98.33% in the product after evaporating and cooling the copper sulfate solution.展开更多
Highly ordered and porous anodic aluminum oxide templates were prepared. The ordered copper nanowires arrays were assembled in nano-holes of the template by alternating current electrodeposition at lover voltage. The ...Highly ordered and porous anodic aluminum oxide templates were prepared. The ordered copper nanowires arrays were assembled in nano-holes of the template by alternating current electrodeposition at lover voltage. The morphologies of template and copper nano-wires arrays were characterized by means of field emission scanning electron microscope (FESEM) and the crystal structure of copper nano-wires was determined by means of X-ray diffraction. The results indicate that copper nano-wires hold the preferred crystalline orientation along (111), (200), (220) and (331) crystal faces during growth, and the growth of copper nano-wires in the nano-holes of the template is homogenous and continuous.展开更多
基金Project(GC200603) supported by the Open Fund of Guangdong Provincial Key Laboratory for Green Chemicals projectsupported by the Key Laboratory of Enhanced Heat Transfer and Energy Conservation of Ministry of Education of China
文摘Bismuth-doped tin dioxide nanometer powders were prepared by co-precipitation method using SnCl4 and Bi（NO3）3 as raw materials. The effects of calcining temperature and doping ratio on the particle size, composition, spectrum selectivity of bismuth-doped tin dioxide and the phase transition of Bi-Sn precursor at different temperatures were studied by means of X-ray diffraction, transmission electron microscopy, ultraviolet-visual-near infrared diffuse reflection spectrum and the thermogravimetric-differential scanning calorimetry. The results show that prepared bismuth-doped tin dioxide powders have excellent characteristics with a single-phase tetragonal structure, good dispersibility, good absorbency for ultraviolet ray and average particle size less than 10 nm. The optimum conditions for preparing bismuth-doped tin dioxide nanometer powders are as follows: calcining temperature of 600℃, ratio of bismuth-doped in a range of 0.10-0.30, and Bi-Sn precursor being dispersed by ultrasonic wave and refluxed azeotropic and distillated with mixture of n-butanol and benzene. The mechanism of phase transition of Bi-Sn precursor is that Bi 3+ enters Sn-vacancy and then forms Sn—O—Bi bond.
文摘The precursors with NiCO3·2Ni（OH）2·2H2O, Fe2O3·nH2O coated alumina microspheres were prepared by the aqueous heterogeneous precipitation using metal salts, ammonium bicarbonate and α-Al2O3 micropowders as the starting materials. Magnetic metal Ni, α-Fe coated alumina, core-shell structural microspheres were successfully obtained by thermal reduction of the precursors at 700℃ for 2h, respectively. Powders of the precursors and the resultant metal （Ni, α-Fe） coated alumina micropowders were characterized by scanning electron microscopy, energy dispersive spectroscopy and X-ray diffraction. The results show that optimized precipitation parameters are concentration of alumina micropowders of 15g/L, rate of adding reactants of 5mL/min and pH value of 7.5. And under the optimized conditions, the spherical precursors without aggregations or agglomerations are obtained, then transferred into Ni, α-Fe coated alumina microspheres by thermal reduction. It is possible to adjust metal coating thicknesses and fabricate a multilayer structured metal/ceramics, core-shell microspherical powder materials.
基金Project(2013A090100013)supported by the Special Project on the Integration of Industry,Education and Research of Guangdong Province,ChinaProject(201407300993)supported by the High-Tech Research and Development Program of Xinjiang Uygur Autonomous Region,China
文摘Proper utilization of the FeSO4·7H2O waste slag generated from TiO2 industry is an urgent need, and Fe3O4 particles are currently being widely used in the wastewater flocculation field. In this work, magnetite was recovered from ferrous sulphate by a novel co-precipitation method with calcium hydroxide as the precipitant. Under optimum conditions, the obtained spherical magnetite particles are well crystallized with a Fe304 purity of 88.78%, but apt to aggregate with a median particle size of 1.83 μm. Magnetic measurement reveals the obtained Fe304 particles are soft magnetic with a saturation magnetization of 81.73 A-m2/kg. In addition, a highly crystallized gypsum co-product is obtained in blocky or irregular shape. Predictably, this study would provide additional opportunities for future application of low-cost Fe3O4 particles in water treatment field.
文摘The solid sodium hydroxide neutralized acidic As-containing wastewater till pH value was 6. Green copper arsenite was prepared after copper sulfate was added into the neutralized wastewater when the molar ratio of Cu to As was 2：1 and pH value of the neutralized wastewater was adjusted to 8.0 by sodium hydroxide. The arsenious acid solution and red residue were produced after copper arsenite mixed with water according to the ratio of liquid to solid of 4：1 and copper arsenite was reduced by SO2 at 60℃ for 1 h. The white powder was gained after the arsenious acid solution was evaporated and cooled. Copper sulfate solution was obtained after the red residue was leached by H2SO4 solution under the action of air. The results show that red residue is Cu3（SO3）2·2H2O and the white powder is As2O3. The leaching rate of Cu reaches 99.00% when the leaching time is 1.5 h, molar ratio of H2SO4 to Cu is 1.70, H2SO4 concentration is 24% and the leaching temperature is 80 ℃. The direct recovery rate of copper sulfate is 79.11% and the content of CuSOa·5H2O is up to 98.33% in the product after evaporating and cooling the copper sulfate solution.
文摘Highly ordered and porous anodic aluminum oxide templates were prepared. The ordered copper nanowires arrays were assembled in nano-holes of the template by alternating current electrodeposition at lover voltage. The morphologies of template and copper nano-wires arrays were characterized by means of field emission scanning electron microscope (FESEM) and the crystal structure of copper nano-wires was determined by means of X-ray diffraction. The results indicate that copper nano-wires hold the preferred crystalline orientation along (111), (200), (220) and (331) crystal faces during growth, and the growth of copper nano-wires in the nano-holes of the template is homogenous and continuous.
