Nanometer ZrO2 - 8% Y2O3 (mole fraction, % ) powders were prepared by the EDTA (ethylenediaminetetraacetic acid) sol-gel process. Effects of the addition of ethylene glycol on agglomerate control was investigated. The...Nanometer ZrO2 - 8% Y2O3 (mole fraction, % ) powders were prepared by the EDTA (ethylenediaminetetraacetic acid) sol-gel process. Effects of the addition of ethylene glycol on agglomerate control was investigated. The results showed that because of the replacement of hydrogen bonds with ethylene glycol in the polymerized gel, gel stabilization and homogeneity were improved and close approach of gel particles was prevented, which led to reduction of hard agglomerates to some extent. Calcined at 4OO t for 2 h and 700 C for 2 h, the powders had a specific surface area of 35 m2/g, average particle size of 28 nm, and median particle size (d50) of 0. 44um with very sharp distribution, mostly being soft agglomerates.展开更多
Two series of perovskite-type oxides with composition (La_(1-x))Sr_xFeO_3(x≤0.8)and La_(1-x)Sr_xFe_(1-y)Co_yO_3(x=0.2; y=0.2, 0.4)powder productions were synthesized by EDTA complexing sol-gel method. The products we...Two series of perovskite-type oxides with composition (La_(1-x))Sr_xFeO_3(x≤0.8)and La_(1-x)Sr_xFe_(1-y)Co_yO_3(x=0.2; y=0.2, 0.4)powder productions were synthesized by EDTA complexing sol-gel method. The products were characterized by XRD, TEM, SEM, BET method(N_2 adsorption)and laser granularity analysis for different synthesis conditions to obtain the optimum conditions for the preparation process. Single-phased, uniform perovskite-type oxides with small particle size were obtained by EDTA sol-gel process with high stability and repeatability, and the process temperature is much lower than that of solid state reaction method.展开更多
A facile EDTA （ethylene diamine tetraacetic acid） complexing technique has been successfully employed to prepare La2Mo2O9 nanoparticles. The as-synthesized products are characterized by X-ray diffraction （XRD）, sc...A facile EDTA （ethylene diamine tetraacetic acid） complexing technique has been successfully employed to prepare La2Mo2O9 nanoparticles. The as-synthesized products are characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, and Fourier transform infrared spectroscopy （FT-IR）. The results show that a homogeneous transparent gel can be obtained with EDTA as the organic complexing reagent under the pH value of 3.0. Further thermal decomposition of the as-synthesized transparent gel by increasing the temperature up to 600℃ for 3 h results in the formation of La2Mo2O9 nanoparticles with a crystal size of about 30 nm. Moreover, the nanoparticles tend to form micrometer-sized aggregates with a three-dimensional network structure, which shows promising applications in solid oxide fuel cells （SOFC）, catalysts and so on.展开更多
A series of (SrNa)2-xEux(MoO4)3 red phosphors have been synthesized by using the sol-gel method. X-ray diffraction, used to characterize the crystallization process of the phosphor precursors, indicates that the (SrNa...A series of (SrNa)2-xEux(MoO4)3 red phosphors have been synthesized by using the sol-gel method. X-ray diffraction, used to characterize the crystallization process of the phosphor precursors, indicates that the (SrNa)2-xEux(MoO4)3 phosphors had an SrMoO4 structure. The properties of these resulting phosphors have also been characterized by using photoluminescence (PL) spectra. The PL results indicate that all of the (SrNa)2-xEux(MoO4)3 phosphors exhibit intense red emissions under 275, 395, and 465-nm excitation. The two strongest lines at 395 and 465 nm in the excitation spectra of these phosphors match well with the two popular emissions from near-UV and blue GaN-based light-emitting diodes. Some process parameters for Eu3+ concentration, (C6H8O7)·H2O concentration, and solution pH value were also investigated. For (SrNa)2-xEux(MoO4)3 phosphors, there are two maximum emission intensities appearing with x = 0.6 and x = 1.4, respectively. When the molar ratio of citric acid is equal to that of metal cations and the solution pH is almost 4, (SrNa)2-xEux(MoO4)3 shows the strongest emission intensity compared to those under other conditions.展开更多
s: Ultrafine A2La2Ti3O10 (A=K, Na) powders with laminar structure were successfully synthesized by citric acid sol-gel method using ANO3(A=K, Na)?La(NO3)3?Ti(OBu)4 and citric acid as starting precursors. The crystalli...s: Ultrafine A2La2Ti3O10 (A=K, Na) powders with laminar structure were successfully synthesized by citric acid sol-gel method using ANO3(A=K, Na)?La(NO3)3?Ti(OBu)4 and citric acid as starting precursors. The crystalline phase of A2La2Ti3O10 can be obtained by thermal decomposition of citrate complex precursors at a relatively low temperature of 800 ℃ (600 ℃ for A=Na), about 300 ℃(500 ℃ for A=Na) lower than that of conventional solid state reaction process. The properties of the citrate precursors and the calcined powders were characterized by Infrared spectroscopy (IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), thermal-gravimetric-differential thermal analysis (TG-DTA), inductively coupled plasma (ICP) and Brunauer-Emmett-Teller (BET) techniques. Results show that the average size of A2La2Ti3O10 powders obtained by citric acid sol-gel route was reduced to 200 nm×250 nm and the specific surface area was up to 19 m2·g-1. At the same time, the product was with more regular morphological characteristics. The synthesis process and the formation of A2La2Ti3O10 were also discussed. The obtained A2La2Ti3O10 was found to be transformed from A2La2Ti3O9.5 during the formation process.展开更多
文摘Nanometer ZrO2 - 8% Y2O3 (mole fraction, % ) powders were prepared by the EDTA (ethylenediaminetetraacetic acid) sol-gel process. Effects of the addition of ethylene glycol on agglomerate control was investigated. The results showed that because of the replacement of hydrogen bonds with ethylene glycol in the polymerized gel, gel stabilization and homogeneity were improved and close approach of gel particles was prevented, which led to reduction of hard agglomerates to some extent. Calcined at 4OO t for 2 h and 700 C for 2 h, the powders had a specific surface area of 35 m2/g, average particle size of 28 nm, and median particle size (d50) of 0. 44um with very sharp distribution, mostly being soft agglomerates.
文摘Two series of perovskite-type oxides with composition (La_(1-x))Sr_xFeO_3(x≤0.8)and La_(1-x)Sr_xFe_(1-y)Co_yO_3(x=0.2; y=0.2, 0.4)powder productions were synthesized by EDTA complexing sol-gel method. The products were characterized by XRD, TEM, SEM, BET method(N_2 adsorption)and laser granularity analysis for different synthesis conditions to obtain the optimum conditions for the preparation process. Single-phased, uniform perovskite-type oxides with small particle size were obtained by EDTA sol-gel process with high stability and repeatability, and the process temperature is much lower than that of solid state reaction method.
基金the Opening Subject of the State Key Laboratory of Powder Metallurgy of China (Nos. 200506123105A and 20070620090631B14)
文摘A facile EDTA （ethylene diamine tetraacetic acid） complexing technique has been successfully employed to prepare La2Mo2O9 nanoparticles. The as-synthesized products are characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, and Fourier transform infrared spectroscopy （FT-IR）. The results show that a homogeneous transparent gel can be obtained with EDTA as the organic complexing reagent under the pH value of 3.0. Further thermal decomposition of the as-synthesized transparent gel by increasing the temperature up to 600℃ for 3 h results in the formation of La2Mo2O9 nanoparticles with a crystal size of about 30 nm. Moreover, the nanoparticles tend to form micrometer-sized aggregates with a three-dimensional network structure, which shows promising applications in solid oxide fuel cells （SOFC）, catalysts and so on.
文摘A series of (SrNa)2-xEux(MoO4)3 red phosphors have been synthesized by using the sol-gel method. X-ray diffraction, used to characterize the crystallization process of the phosphor precursors, indicates that the (SrNa)2-xEux(MoO4)3 phosphors had an SrMoO4 structure. The properties of these resulting phosphors have also been characterized by using photoluminescence (PL) spectra. The PL results indicate that all of the (SrNa)2-xEux(MoO4)3 phosphors exhibit intense red emissions under 275, 395, and 465-nm excitation. The two strongest lines at 395 and 465 nm in the excitation spectra of these phosphors match well with the two popular emissions from near-UV and blue GaN-based light-emitting diodes. Some process parameters for Eu3+ concentration, (C6H8O7)·H2O concentration, and solution pH value were also investigated. For (SrNa)2-xEux(MoO4)3 phosphors, there are two maximum emission intensities appearing with x = 0.6 and x = 1.4, respectively. When the molar ratio of citric acid is equal to that of metal cations and the solution pH is almost 4, (SrNa)2-xEux(MoO4)3 shows the strongest emission intensity compared to those under other conditions.
文摘s: Ultrafine A2La2Ti3O10 (A=K, Na) powders with laminar structure were successfully synthesized by citric acid sol-gel method using ANO3(A=K, Na)?La(NO3)3?Ti(OBu)4 and citric acid as starting precursors. The crystalline phase of A2La2Ti3O10 can be obtained by thermal decomposition of citrate complex precursors at a relatively low temperature of 800 ℃ (600 ℃ for A=Na), about 300 ℃(500 ℃ for A=Na) lower than that of conventional solid state reaction process. The properties of the citrate precursors and the calcined powders were characterized by Infrared spectroscopy (IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), thermal-gravimetric-differential thermal analysis (TG-DTA), inductively coupled plasma (ICP) and Brunauer-Emmett-Teller (BET) techniques. Results show that the average size of A2La2Ti3O10 powders obtained by citric acid sol-gel route was reduced to 200 nm×250 nm and the specific surface area was up to 19 m2·g-1. At the same time, the product was with more regular morphological characteristics. The synthesis process and the formation of A2La2Ti3O10 were also discussed. The obtained A2La2Ti3O10 was found to be transformed from A2La2Ti3O9.5 during the formation process.
