The precursor prepared by coordinated co-precipitation was direct reduced by hydrogen to ultra-fine fibrous Fe-Ni alloy powder. The effects of concentrations of reactants, pH value, reaction temperature and additive o...The precursor prepared by coordinated co-precipitation was direct reduced by hydrogen to ultra-fine fibrous Fe-Ni alloy powder. The effects of concentrations of reactants, pH value, reaction temperature and additive on the preparation of precursor were systematically investigated. The structures, thermal decomposition processes and morphologies of the precursors were characterized by X-ray diffraction (XRD), thermal gravity-differential thermal analysis (TG-DTA) and scanning electron microscoy (SEM). The results show that using 2% polyvinylpyrrolidone (PVP) (in mass fraction) as additive, a well-dispersed precursor with a uniform morphology can be obtained in a solution with Fe2+ and Ni2+ total concentration (1:1) of 0.8 mol/L, pH value of 6.2 at 60 °C, and a pure and well dispersed fibrous iron-nickel powder can be prepared by direct reduction of this precursor in a mixed atmosphere of nitrogen and hydrogen at the temperature of 420 °C.展开更多
A novel precursor of nickel-cobalt alloy powders with an appropriate Ni to Co molar ratio was prepared under selectively synthetic conditions. The composition and morphology of the precursor were characterized by X-ra...A novel precursor of nickel-cobalt alloy powders with an appropriate Ni to Co molar ratio was prepared under selectively synthetic conditions. The composition and morphology of the precursor were characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, Fourier transform infrared spectrometry （FT-IR） and energy dispersive spectrometry （EDS）. The effects of pH value, reaction temperature, metal ion concentrations and surfactant on the morphology and the dispersion of precursor were investigated. The results show that the morphology of precursor depends on ammonia content in the precursor. A fibriform precursor is a complicated ammonia-containing nickel-cobalt oxalate. The uniform shape-controlled fibrous precursor is obtained under the following optimum conditions： ammonia as complex agent as well as pH adjustor, oxalate as coprecipitator, 50-65 °C of reaction temperature, 0.5-0.8 mol/L of total concentration of Ni2＋ and Co2＋, PVP as dispersant, and pH 8.0-8.4.展开更多
Red-emission （Y0.95Eu0.05）2O3 submicron spheres and microplates were selectively obtained via hydrothermal precursor synthesis （150 °C, 12 h） followed by calcination at 1000 °C. Characterizations of the ...Red-emission （Y0.95Eu0.05）2O3 submicron spheres and microplates were selectively obtained via hydrothermal precursor synthesis （150 °C, 12 h） followed by calcination at 1000 °C. Characterizations of the products were carried out by combined means of XRD, FT-IR, FE-SEM and PL analysis. The precursors could be modulated from basic-carbonate submicron spheres to normal carbonate microplates by increasing the molar ratio of urea to Y＋Eu from 10 to 40-100. The resultant oxides largely retain their respective precursor morphologies at 1000 °C, but morphology confined crystal growth was observed for the microplates, yielding more enhanced exposure of the （400） facets. Both the （Y0.95Eu0.05）2O3 spheres and microplates exhibit nearly identical positions of the PL bands and similar asymmetry factors of luminescence [I（5D0→7F2）/I（5D0→7F1）, ～11] under 250 nm excitation, but the microplates show a significantly strong red emission at ～613 nm （ ～1.33 times that of the spheres） owing to their larger particle size and denser packing of primary phosphor crystallites.展开更多
基金Project (20090162120080) supported by the Research Fund for Doctoral Program of Higher Education of ChinaProject (2010FJ3011)supported by the Program of Science and Technology of Hunan Province, ChinaProject supported by the Open-End Fund for the Valuable and Precision Instruments of Central South University, China
文摘The precursor prepared by coordinated co-precipitation was direct reduced by hydrogen to ultra-fine fibrous Fe-Ni alloy powder. The effects of concentrations of reactants, pH value, reaction temperature and additive on the preparation of precursor were systematically investigated. The structures, thermal decomposition processes and morphologies of the precursors were characterized by X-ray diffraction (XRD), thermal gravity-differential thermal analysis (TG-DTA) and scanning electron microscoy (SEM). The results show that using 2% polyvinylpyrrolidone (PVP) (in mass fraction) as additive, a well-dispersed precursor with a uniform morphology can be obtained in a solution with Fe2+ and Ni2+ total concentration (1:1) of 0.8 mol/L, pH value of 6.2 at 60 °C, and a pure and well dispersed fibrous iron-nickel powder can be prepared by direct reduction of this precursor in a mixed atmosphere of nitrogen and hydrogen at the temperature of 420 °C.
基金Project (20090162120080) supported by Doctoral Fund of Ministry of Education, ChinaProject (20070410989) supported by China Postdoctoral Science FoundationProject(748310000) supported by Central South University Science Foundation for Youths, China
文摘A novel precursor of nickel-cobalt alloy powders with an appropriate Ni to Co molar ratio was prepared under selectively synthetic conditions. The composition and morphology of the precursor were characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, Fourier transform infrared spectrometry （FT-IR） and energy dispersive spectrometry （EDS）. The effects of pH value, reaction temperature, metal ion concentrations and surfactant on the morphology and the dispersion of precursor were investigated. The results show that the morphology of precursor depends on ammonia content in the precursor. A fibriform precursor is a complicated ammonia-containing nickel-cobalt oxalate. The uniform shape-controlled fibrous precursor is obtained under the following optimum conditions： ammonia as complex agent as well as pH adjustor, oxalate as coprecipitator, 50-65 °C of reaction temperature, 0.5-0.8 mol/L of total concentration of Ni2＋ and Co2＋, PVP as dispersant, and pH 8.0-8.4.
基金Projects (50172030, 50972025, 50990303, 51172038) supported by the National Natural Science Foundation of ChinaProject supported by the Liaoning BaiQianWan Talents Program, China+1 种基金Projects (N110802001, N100702001) supported by the Fundamental Research Funds for the Central Universities, ChinaProject supported by the China Scholarship Council
文摘Red-emission （Y0.95Eu0.05）2O3 submicron spheres and microplates were selectively obtained via hydrothermal precursor synthesis （150 °C, 12 h） followed by calcination at 1000 °C. Characterizations of the products were carried out by combined means of XRD, FT-IR, FE-SEM and PL analysis. The precursors could be modulated from basic-carbonate submicron spheres to normal carbonate microplates by increasing the molar ratio of urea to Y＋Eu from 10 to 40-100. The resultant oxides largely retain their respective precursor morphologies at 1000 °C, but morphology confined crystal growth was observed for the microplates, yielding more enhanced exposure of the （400） facets. Both the （Y0.95Eu0.05）2O3 spheres and microplates exhibit nearly identical positions of the PL bands and similar asymmetry factors of luminescence [I（5D0→7F2）/I（5D0→7F1）, ～11] under 250 nm excitation, but the microplates show a significantly strong red emission at ～613 nm （ ～1.33 times that of the spheres） owing to their larger particle size and denser packing of primary phosphor crystallites.
