MnZn ferrites with the chemical formula Mn0.68Zn0.25Fe2.07O4 have been prepared by a conventional ceramic technique. Then, the effects of CuO addition on the microstructure and temperature dependence of magnetic prope...MnZn ferrites with the chemical formula Mn0.68Zn0.25Fe2.07O4 have been prepared by a conventional ceramic technique. Then, the effects of CuO addition on the microstructure and temperature dependence of magnetic properties of MnZn ferrites were investigated by characterizing the fracture surface micrograph and measuring the magnetic properties over a temperature ranging from 25 to 120 C. The results show that the lattice constant and average grain size increase with the increase of CuO concentration. When the CuO concentration is below 0.07 wt.%, the initial permeability and saturation magnetic flux density increase monotonously, and the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a lower temperature with the increase of CuO concentra-tion. However, excessive CuO concentration (0.07 wt.%) results in abnormal grain growth and porosity increase, which causes the initial permeability and saturation magnetic flux density decrease and the power loss increase at room temperature. Furthermore, the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a higher temperature.展开更多
NiFe2O4 nanorods have been successfully synthesized via thermal treatment of the rod-like precursor fabricated by Ni-doped (x-FeOOH, which was enwrapped by the complex of citric acid and Niz~. The morphology evolutio...NiFe2O4 nanorods have been successfully synthesized via thermal treatment of the rod-like precursor fabricated by Ni-doped (x-FeOOH, which was enwrapped by the complex of citric acid and Niz~. The morphology evolution during the calcination of the precursor nanorods was investigated with transmission electron microscopy (TEM), and the phase and the magnetic properties of samples were analyzed through X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). The results indicated that the diameter of the NiFe204 nanorods obtained ranged between 30 and 50 nm, and the length ranged between 2 and 3 um. As the calcination temperature was up to 600℃, the coercivity, saturation magnetization, and remanent magnetization of the samples were 36.1 kA.m^-1, 27.2 A.m2.kg^-1, and 5.3 A.m2.kg^-1, respectively. The NiFe2O4 nanorods prepared have higher shape anisotropy and superior magnetic properties than those with irregular shapes.展开更多
Fe(OH)3 precursor sol was prepared by a sol-gel method. The precursor sol was dipped onto the absorbent cotton, and gel was formed on the absorbent cotton template after the volatilization of moisture. Fe2O3 microtu...Fe(OH)3 precursor sol was prepared by a sol-gel method. The precursor sol was dipped onto the absorbent cotton, and gel was formed on the absorbent cotton template after the volatilization of moisture. Fe2O3 microtubules were synthesized after the process of self-propagation or calcination. The phase, morphology, and particle diameter of the samples were examined by X-ray diffraction (XRD) and scanning electron microscopy (SEM), and the magnetic properties of the samples were measured using a vibrating sample magnetometer (VSM). The external diameters of Fe2O3 microtubules ranged between 8 and 13 μm, and the wall thicknesses ranged between 0.5 and 2 μm. The type of the calcination method plays a significant role in developing the Fe2O3 phase and the variation in the magnetic properties in the sol-gel template complexing method. γ-Fe2O3 was synthesized by a self-propagation method. However, α-Fe203 was synthesized after calcination at 400℃ for 2 h. The coercivity of the samples synthesized by calcination at 400℃ for 2 h after self-propagation was found to increase significantly, thereby presenting hard magnetic properties.展开更多
In this paper, we report the preparation of nickel phosphate in aqueous solution and its use as inorganic pigment. Because cerium phosphate is insoluble in acidic and basic solution, the addition of cerium was tried t...In this paper, we report the preparation of nickel phosphate in aqueous solution and its use as inorganic pigment. Because cerium phosphate is insoluble in acidic and basic solution, the addition of cerium was tried to improve the acid and base resistance of nickel phosphate pigment. The cerium substituted nickel phosphates were prepared from phosphoric acid, nickel nitrate, and ammonium cerium nitrate solution. The additional effects of tetravalent cerium cation were studied on the chemical composition, particle shape and size distribution, specific surface area, color, acid and base resistance of the precipitates and their thermal products.展开更多
The layered cobaltite Ca 2.6Nd 0.4Co 4O 9 was synthesized by the solid-state reaction. Their crystal structure was determined by the X-ray powder diffraction and CELL program. The prepared Ca 2.6Nd 0.4Co...The layered cobaltite Ca 2.6Nd 0.4Co 4O 9 was synthesized by the solid-state reaction. Their crystal structure was determined by the X-ray powder diffraction and CELL program. The prepared Ca 2.6Nd 0.4Co 4O 9 compound has the monoclinic symmetry. The electrical conductivity and Seebeck coefficient were measured from room temperature to 700 ℃ in air. Both the properties increase while rising temperature. The thermoelectric power of Ca 2.6Nd 0.4Co 4O 9 is about 242 4 μV·K -1. The results imply a promising way to enhance the thermoelectric properties of the layered cobaltite oxides by optimizing their composition and microstructure.展开更多
Layered hydroxide metal acetate Co2(OH)3(CH3COO)·H2O with an interlayer spacing of 1.282 nm has been synthesized by a novel method which is employed in ethanol-aqueous mixed solvents media. Experiment results...Layered hydroxide metal acetate Co2(OH)3(CH3COO)·H2O with an interlayer spacing of 1.282 nm has been synthesized by a novel method which is employed in ethanol-aqueous mixed solvents media. Experiment results show that the purity of the product by the modified method is higher compared with that by the previous methods. A complete characterization of the as-prepared samples was performed by means of X-ray powder diffraction, IR spectroscopy, scanning electron microscope, as well as magnetic measurement. The facile and effective approach for the preparation of this compound in this study is very interesting and important because it has wide application in the field of anionic exchange reaction for the synthesis of hybrid organic-inorganic compounds.展开更多
The photocatalytic degradation of 4-chlorophenol (4-CP) in aqueous solution was studied using Cu-MoO4- doped TiO2 nanoparticles under Visible light radiation. The photocatalysts were synthesized by chemical route from...The photocatalytic degradation of 4-chlorophenol (4-CP) in aqueous solution was studied using Cu-MoO4- doped TiO2 nanoparticles under Visible light radiation. The photocatalysts were synthesized by chemical route from TiO2 with different concentration of CuMoO4 (CuxMoxTi1-xO6;where, x values ranged from 0.05 to 0.5). The prepared nanoparticles are characterized by XRD, BET surface area, TEM, UV-vis diffuse reflectance spectra, Raman spectroscopy, XPS and EDAX spectroscopy were used to investigate the nanoparticles structure, size distribution, and qualitative elemental analysis of the composition. The CuxMoxTi1-xO6 (x = 0.05) showed high activity for degradation of 4-CP under visible light. The surface area of the catalyst was found to be 101 m2/g. The photodegradation process was optimized by using CuxMoxTi1-xO6 (x = 0.05) catalyst at a concentration level of 1 g/l. A maximum photocatalytic efficiency of 96.9% was reached at pH = 9 after irradiation for 3 hours. Parameters affecting the photocatalytic process such as catalyst loading, concentration of the catalyst and the dopant concentration, solution pH, and concentration of 4-CP have been investigated.展开更多
With coaxial nozzle system, TiO2 hollow spheres were prepared and the optimum parameters of forming TiO2 hollow spheres were fix on as follows: acrylamide (AM) was used as monomer up to 30.3%, acetone was used as vesi...With coaxial nozzle system, TiO2 hollow spheres were prepared and the optimum parameters of forming TiO2 hollow spheres were fix on as follows: acrylamide (AM) was used as monomer up to 30.3%, acetone was used as vesicant, the mass fraction of initiator was 0.4%, the forming temperature was in the range from 90 ℃ to 95 ℃. The photocatalistic performance of TiO2 hollow spheres was characterized by degradation of methyl orange. Compared with nano-TiO2 powders, hollow spheres can be recycled after cleanout and drying, taking on similar efficiency of photocatalistic.展开更多
Hexagonal yb3+,Er3+-doped NaYF4 crystals with different morphologies were synthesized by a facile hydrothermal method at 140-200 ℃. Their shape and size could be controlled by varying hydrothermal temperature, time...Hexagonal yb3+,Er3+-doped NaYF4 crystals with different morphologies were synthesized by a facile hydrothermal method at 140-200 ℃. Their shape and size could be controlled by varying hydrothermal temperature, time and doping effect of Ce3+ ions. Interestingly, the products displayed hexagonal sheet, plate, crown-like prism to tube changes in the temperature range from 140 to 200 ℃. A combination of "diffusion-controlled growth" and "selective adsorption" was proposed to understand the formation of the NaYF4 crystals with well-defined shapes. NaYF4:yb3+/Er3+ crystals exhibited shape-dependent up-conversion (UC) luminescence under excitation of 980 nm, and their luminescence property could be tuned by doping Ce3+ ions.展开更多
Owing to the excellent elastic properties and chemical stability,binary metal or light element borides,carbides and nitrides have been extensively applied as hard and low-compressible materials.Researchers are searchi...Owing to the excellent elastic properties and chemical stability,binary metal or light element borides,carbides and nitrides have been extensively applied as hard and low-compressible materials.Researchers are searching for harder materials all the time.Recently,the successful fabrication of nano-twinned cubic BN(Tian et al.Nature 493:385–388,2013)and diamond(Huang et al.Nature 510:250–253,2014)exhibiting superior properties than their twin-free counterparts allows an efficient way to be harder.From this point of view,the borides,carbides and nitrides may be stronger by introducing twins,whose formation tendency can be measured using stacking fault energies(SFEs).The lower the SFEs,the easier the formation of twins.In the present study,by means of first-principles calculations,we first calculated the fundamental elastic constants of forty-two borides,seventeen carbides and thirty-one nitrides,and their moduli,elastic anisotropy factors and bonding characters were accordingly derived.Then,the SFEs of the{111}<112>glide system of twenty-seven compounds with the space group F43 m or Fm3m were calculated.Based on the obtained elastic properties and SFEs,we find that(1)light element compounds usually exhibit superior elastic properties over the metal borides,carbides or nitrides;(2)the 5 d transitionmetal compounds(ReB2,WB,OsC,RuC,WC,OsN2,TaN and WN)possess comparable bulk modulus(B)with that of cBN(B=363 GPa);(3)twins may form in ZrB,HfN,PtN,VN and ZrN,since their SFEs are lower or slightly higher than that of diamond(SFE=277 mJ/m^2).Our work can be used as a valuable database to compare these compounds.展开更多
Neodymium-doped barium phosphate(NdBP)was prepared as single crystal by room temperature solution technique known as gel encapsulation technique.Single crystal X-ray diffraction shows that the crystal belongs to ortho...Neodymium-doped barium phosphate(NdBP)was prepared as single crystal by room temperature solution technique known as gel encapsulation technique.Single crystal X-ray diffraction shows that the crystal belongs to orthorthombic system.The flower type morphology was observed by scanning electron microscope(SEM)and the stoichiometric composition of the prepared crystal was observed by energy dispersive X-ray analysis(EDAX).The presence of functional group and other groups was studied by Fourier transform infrared spectroscopy(FTIR).The electrical properties of these materials like dielectric constant(ε′),dieletric loss(tan σ)and ac conductivity[ln(σac)]was studied at different temperatures ranging from 40℃ to 420℃ in the frequency range of 5 kHz to 1 MHz.The activation energy values decreases with increase in frequency suggesting that the conduction mechanism is because of hopping of charge carriers.展开更多
Zn1-xMnxS (x = 0-0.05) nanorods were successfully synthesized through a hydrothermal route. The morphology, composition and microstructure of Zn1-xMnxS nanorods were characterized respectively by X-ray diffraction ...Zn1-xMnxS (x = 0-0.05) nanorods were successfully synthesized through a hydrothermal route. The morphology, composition and microstructure of Zn1-xMnxS nanorods were characterized respectively by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectrometer. The optical properties of Zn1-xMnxS nanorods were determineded by UV-Vis absorption spectroscopy and photo- luminescence (PL) emission spectroscopy. The results show that the introduction of Mn^2+ on interstitial sites in ZnS lattice has significant influence on the Raman spectra, UV-Vis absorption spectra and PL emis- sion spectra. With the increase of Mn^2+, the lengths of the sampled nanorods become shorter and the morphologies of the products show disorder accompanied by some nanoparticles. The absorption band edge shifts to longer wavelength. The intensity of the ZnS-related emission gradually becomes weaker, whereas, the Mn^2+-related broad emission spectra located at 580 nm gradually red-shifts and increases. Occupation of Zn^2+ sites in the lattice by Mn^2+ ions results in lattice distortion and influences the energy level structure of ZnS. The Mn doping is found responsible for the changes in the defect-related emission of the ZnS nanorods.展开更多
文摘MnZn ferrites with the chemical formula Mn0.68Zn0.25Fe2.07O4 have been prepared by a conventional ceramic technique. Then, the effects of CuO addition on the microstructure and temperature dependence of magnetic properties of MnZn ferrites were investigated by characterizing the fracture surface micrograph and measuring the magnetic properties over a temperature ranging from 25 to 120 C. The results show that the lattice constant and average grain size increase with the increase of CuO concentration. When the CuO concentration is below 0.07 wt.%, the initial permeability and saturation magnetic flux density increase monotonously, and the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a lower temperature with the increase of CuO concentra-tion. However, excessive CuO concentration (0.07 wt.%) results in abnormal grain growth and porosity increase, which causes the initial permeability and saturation magnetic flux density decrease and the power loss increase at room temperature. Furthermore, the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a higher temperature.
基金the North University of China and the National Natural Science Foundation of China (No50535030) for financial support to this work
文摘NiFe2O4 nanorods have been successfully synthesized via thermal treatment of the rod-like precursor fabricated by Ni-doped (x-FeOOH, which was enwrapped by the complex of citric acid and Niz~. The morphology evolution during the calcination of the precursor nanorods was investigated with transmission electron microscopy (TEM), and the phase and the magnetic properties of samples were analyzed through X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). The results indicated that the diameter of the NiFe204 nanorods obtained ranged between 30 and 50 nm, and the length ranged between 2 and 3 um. As the calcination temperature was up to 600℃, the coercivity, saturation magnetization, and remanent magnetization of the samples were 36.1 kA.m^-1, 27.2 A.m2.kg^-1, and 5.3 A.m2.kg^-1, respectively. The NiFe2O4 nanorods prepared have higher shape anisotropy and superior magnetic properties than those with irregular shapes.
基金the North University of China for the support given for carrying out this work under projects from the National Natural Science Fundation of China(Nos.20571066 and 20871108)
文摘Fe(OH)3 precursor sol was prepared by a sol-gel method. The precursor sol was dipped onto the absorbent cotton, and gel was formed on the absorbent cotton template after the volatilization of moisture. Fe2O3 microtubules were synthesized after the process of self-propagation or calcination. The phase, morphology, and particle diameter of the samples were examined by X-ray diffraction (XRD) and scanning electron microscopy (SEM), and the magnetic properties of the samples were measured using a vibrating sample magnetometer (VSM). The external diameters of Fe2O3 microtubules ranged between 8 and 13 μm, and the wall thicknesses ranged between 0.5 and 2 μm. The type of the calcination method plays a significant role in developing the Fe2O3 phase and the variation in the magnetic properties in the sol-gel template complexing method. γ-Fe2O3 was synthesized by a self-propagation method. However, α-Fe203 was synthesized after calcination at 400℃ for 2 h. The coercivity of the samples synthesized by calcination at 400℃ for 2 h after self-propagation was found to increase significantly, thereby presenting hard magnetic properties.
文摘In this paper, we report the preparation of nickel phosphate in aqueous solution and its use as inorganic pigment. Because cerium phosphate is insoluble in acidic and basic solution, the addition of cerium was tried to improve the acid and base resistance of nickel phosphate pigment. The cerium substituted nickel phosphates were prepared from phosphoric acid, nickel nitrate, and ammonium cerium nitrate solution. The additional effects of tetravalent cerium cation were studied on the chemical composition, particle shape and size distribution, specific surface area, color, acid and base resistance of the precipitates and their thermal products.
文摘The layered cobaltite Ca 2.6Nd 0.4Co 4O 9 was synthesized by the solid-state reaction. Their crystal structure was determined by the X-ray powder diffraction and CELL program. The prepared Ca 2.6Nd 0.4Co 4O 9 compound has the monoclinic symmetry. The electrical conductivity and Seebeck coefficient were measured from room temperature to 700 ℃ in air. Both the properties increase while rising temperature. The thermoelectric power of Ca 2.6Nd 0.4Co 4O 9 is about 242 4 μV·K -1. The results imply a promising way to enhance the thermoelectric properties of the layered cobaltite oxides by optimizing their composition and microstructure.
基金Supported by the President Fund of Xi'an Technological University,China(No.XAGDXJJ1009)
文摘Layered hydroxide metal acetate Co2(OH)3(CH3COO)·H2O with an interlayer spacing of 1.282 nm has been synthesized by a novel method which is employed in ethanol-aqueous mixed solvents media. Experiment results show that the purity of the product by the modified method is higher compared with that by the previous methods. A complete characterization of the as-prepared samples was performed by means of X-ray powder diffraction, IR spectroscopy, scanning electron microscope, as well as magnetic measurement. The facile and effective approach for the preparation of this compound in this study is very interesting and important because it has wide application in the field of anionic exchange reaction for the synthesis of hybrid organic-inorganic compounds.
文摘The photocatalytic degradation of 4-chlorophenol (4-CP) in aqueous solution was studied using Cu-MoO4- doped TiO2 nanoparticles under Visible light radiation. The photocatalysts were synthesized by chemical route from TiO2 with different concentration of CuMoO4 (CuxMoxTi1-xO6;where, x values ranged from 0.05 to 0.5). The prepared nanoparticles are characterized by XRD, BET surface area, TEM, UV-vis diffuse reflectance spectra, Raman spectroscopy, XPS and EDAX spectroscopy were used to investigate the nanoparticles structure, size distribution, and qualitative elemental analysis of the composition. The CuxMoxTi1-xO6 (x = 0.05) showed high activity for degradation of 4-CP under visible light. The surface area of the catalyst was found to be 101 m2/g. The photodegradation process was optimized by using CuxMoxTi1-xO6 (x = 0.05) catalyst at a concentration level of 1 g/l. A maximum photocatalytic efficiency of 96.9% was reached at pH = 9 after irradiation for 3 hours. Parameters affecting the photocatalytic process such as catalyst loading, concentration of the catalyst and the dopant concentration, solution pH, and concentration of 4-CP have been investigated.
文摘With coaxial nozzle system, TiO2 hollow spheres were prepared and the optimum parameters of forming TiO2 hollow spheres were fix on as follows: acrylamide (AM) was used as monomer up to 30.3%, acetone was used as vesicant, the mass fraction of initiator was 0.4%, the forming temperature was in the range from 90 ℃ to 95 ℃. The photocatalistic performance of TiO2 hollow spheres was characterized by degradation of methyl orange. Compared with nano-TiO2 powders, hollow spheres can be recycled after cleanout and drying, taking on similar efficiency of photocatalistic.
基金Project supported by the National Natural Science Foundation of China(20671029,21271062Major State Basic Research Development Program of China(2013CBA01700)
文摘Hexagonal yb3+,Er3+-doped NaYF4 crystals with different morphologies were synthesized by a facile hydrothermal method at 140-200 ℃. Their shape and size could be controlled by varying hydrothermal temperature, time and doping effect of Ce3+ ions. Interestingly, the products displayed hexagonal sheet, plate, crown-like prism to tube changes in the temperature range from 140 to 200 ℃. A combination of "diffusion-controlled growth" and "selective adsorption" was proposed to understand the formation of the NaYF4 crystals with well-defined shapes. NaYF4:yb3+/Er3+ crystals exhibited shape-dependent up-conversion (UC) luminescence under excitation of 980 nm, and their luminescence property could be tuned by doping Ce3+ ions.
基金supported by the National Natural Science Foundation of China (Nos. 11427806, 51471067, 51671082, 51671086 and 51302313)the National Key Research and Development Program of China (No. 2016YFB0300801)
文摘Owing to the excellent elastic properties and chemical stability,binary metal or light element borides,carbides and nitrides have been extensively applied as hard and low-compressible materials.Researchers are searching for harder materials all the time.Recently,the successful fabrication of nano-twinned cubic BN(Tian et al.Nature 493:385–388,2013)and diamond(Huang et al.Nature 510:250–253,2014)exhibiting superior properties than their twin-free counterparts allows an efficient way to be harder.From this point of view,the borides,carbides and nitrides may be stronger by introducing twins,whose formation tendency can be measured using stacking fault energies(SFEs).The lower the SFEs,the easier the formation of twins.In the present study,by means of first-principles calculations,we first calculated the fundamental elastic constants of forty-two borides,seventeen carbides and thirty-one nitrides,and their moduli,elastic anisotropy factors and bonding characters were accordingly derived.Then,the SFEs of the{111}<112>glide system of twenty-seven compounds with the space group F43 m or Fm3m were calculated.Based on the obtained elastic properties and SFEs,we find that(1)light element compounds usually exhibit superior elastic properties over the metal borides,carbides or nitrides;(2)the 5 d transitionmetal compounds(ReB2,WB,OsC,RuC,WC,OsN2,TaN and WN)possess comparable bulk modulus(B)with that of cBN(B=363 GPa);(3)twins may form in ZrB,HfN,PtN,VN and ZrN,since their SFEs are lower or slightly higher than that of diamond(SFE=277 mJ/m^2).Our work can be used as a valuable database to compare these compounds.
文摘Neodymium-doped barium phosphate(NdBP)was prepared as single crystal by room temperature solution technique known as gel encapsulation technique.Single crystal X-ray diffraction shows that the crystal belongs to orthorthombic system.The flower type morphology was observed by scanning electron microscope(SEM)and the stoichiometric composition of the prepared crystal was observed by energy dispersive X-ray analysis(EDAX).The presence of functional group and other groups was studied by Fourier transform infrared spectroscopy(FTIR).The electrical properties of these materials like dielectric constant(ε′),dieletric loss(tan σ)and ac conductivity[ln(σac)]was studied at different temperatures ranging from 40℃ to 420℃ in the frequency range of 5 kHz to 1 MHz.The activation energy values decreases with increase in frequency suggesting that the conduction mechanism is because of hopping of charge carriers.
基金funded by Guangdong Natural Science Foundation of China (Nos. 06029274, 91525000 and 02000003)Guangdong Science & Technology Project of China (No.2008B080702003)
文摘Zn1-xMnxS (x = 0-0.05) nanorods were successfully synthesized through a hydrothermal route. The morphology, composition and microstructure of Zn1-xMnxS nanorods were characterized respectively by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectrometer. The optical properties of Zn1-xMnxS nanorods were determineded by UV-Vis absorption spectroscopy and photo- luminescence (PL) emission spectroscopy. The results show that the introduction of Mn^2+ on interstitial sites in ZnS lattice has significant influence on the Raman spectra, UV-Vis absorption spectra and PL emis- sion spectra. With the increase of Mn^2+, the lengths of the sampled nanorods become shorter and the morphologies of the products show disorder accompanied by some nanoparticles. The absorption band edge shifts to longer wavelength. The intensity of the ZnS-related emission gradually becomes weaker, whereas, the Mn^2+-related broad emission spectra located at 580 nm gradually red-shifts and increases. Occupation of Zn^2+ sites in the lattice by Mn^2+ ions results in lattice distortion and influences the energy level structure of ZnS. The Mn doping is found responsible for the changes in the defect-related emission of the ZnS nanorods.