The doping effects of rare earth oxides Ho_2O_3 and Er_2O_3 on dielectric properties of BaTiO_3-based ceramics were studied. After adding rare earth elements, grain growth in this system was inhibited and the grain si...The doping effects of rare earth oxides Ho_2O_3 and Er_2O_3 on dielectric properties of BaTiO_3-based ceramics were studied. After adding rare earth elements, grain growth in this system was inhibited and the grain size was reduced evidently which realized the fine-grained effect. In this system, the trivalent oxides Ho_2O_3 and Er_2O_3 were added to BaTiO_3 ceramics. The rare earth oxides do not enter into inner lattice totally to replace A or B sites. Some of additives can improve dielectric strength by forming nonferroelectric phases, and the rest maintained at grain boundaries controls overgrowth of grains. The dielectric constant at room temperature is increased up to 3000 and the curve of TCC becomes flat. Meanwhile, the dielectric strength E_b becomes higher.展开更多
The primariy application of rare - earth spin finishes on PET/PA composite super - fine denier fiber has been studied in this paper. It results in the improvement of fi-ber’s properties, such as increased whiteness, ...The primariy application of rare - earth spin finishes on PET/PA composite super - fine denier fiber has been studied in this paper. It results in the improvement of fi-ber’s properties, such as increased whiteness, brightness and brilliance, effective and uniform spliting of compos-ite fiber into super - fine denier fiber and enhanced dye-ing effect.展开更多
Cerium carbonate powders were produced in a submerged circulation impinging stream reactor （SCISR） from Ce（NO3）3· 6H2O. NH4HCO3 was used as a precipitant in the reaction. Cerium carbonate powders were roasted...Cerium carbonate powders were produced in a submerged circulation impinging stream reactor （SCISR） from Ce（NO3）3· 6H2O. NH4HCO3 was used as a precipitant in the reaction. Cerium carbonate powders were roasted to produce ultra-fine cerium dioxide （CeO2） powders. The optimal conditions of such production process were obtained by orthogonal and one-factor experiments. The results showed that ultra-fine and narrowly distributed cerium carbonate powders were produced under the optimal flowing conditions. The concentrations of Ce（NO3）3 and NH4HCO3 solutions were 02,5 and 0.3 mol · L^-1, respectively. The concentration of PEG4000 added in these two solutions was 4 g · L^-1. The stirring ratio, reaction temperature, feeding time, solution pH, reaction time and digestion time were 900 r · min^- 1,80 ℃, 20 min, 5 - 6, 5 min and 1 h, respectively. The final product, CeO2 powders, was obtained by roasting the produced cerium carbonate in air for 3 h at 500 ℃. The finally produced CeO2 powders were torispherical particles with a narrow size distribution of 0.8 -2.5 μm. The crystal structure of CeO2 powders belonged to cubic crystal system and its space point 5 group was OH^5-FM3M. Under optimal conditions, powders produced by SCISR were finer and more narrowly distributed than that by Stirred Tank Reactor （STR）.展开更多
Ultra-fine CeO_2-ZrO_2 mixed oxide was successfully synthesized by wet-solid phase mechanochemical processing, Ce_2(CO_3)_3·8H_2O, ZrOCl_2·xH_2O and ammonia were used as reactants. It is found that the cryst...Ultra-fine CeO_2-ZrO_2 mixed oxide was successfully synthesized by wet-solid phase mechanochemical processing, Ce_2(CO_3)_3·8H_2O, ZrOCl_2·xH_2O and ammonia were used as reactants. It is found that the crystalline Ce_2(CO_3)_3·8H_2O and ZrOCl_2·xH_2O are changed to amorphous cerium and zirconium hydroxide precursor after milling with ammonia, and Ce_(0.15)Zr_(0.85)O_2 mixed oxide with pure tetragonal phase structure and medium particle size(D_(50))less than 1μm is formed by calcining precursor over 673 K. The XRD patterns indicate that the crystal unite size increases with rising calcining temperature due to crystal growth. However, the particle size and BET surface area of the Ce(Zr)O_2 mixed oxide decreases with rising calcining temperature, which may be attributed to the contract of particles and the vanish of holes inside grains.展开更多
Fine spherical particle sized ceria (CeO_2) was prepared by homogeneous precipitation method with ammonium bicarbonate as precipitant. The prepared CeO_2 has the primary particle size of 10～50 nm when calcined betwee...Fine spherical particle sized ceria (CeO_2) was prepared by homogeneous precipitation method with ammonium bicarbonate as precipitant. The prepared CeO_2 has the primary particle size of 10～50 nm when calcined between 400～700 ℃ analyzed by XRD and the aggregated particle size is about 300 nm measured by LASER particle sizer. SEM, TG-DTA and Zeta-potential analyzer were employed individually to study the morphology and the formation of CeO_2 product. It was found that excess NH_4NO_3 can serve as an sphericallization agent to prepare spherical CeO_2 powder by precipitation method.展开更多
The influence of Pr6O11 on the microstructure of ZnO varistors was researched. The results of experiment indicate that addition of Pr6O11 leads to the change of the formation process of the spinel phase. A lot of pyro...The influence of Pr6O11 on the microstructure of ZnO varistors was researched. The results of experiment indicate that addition of Pr6O11 leads to the change of the formation process of the spinel phase. A lot of pyrochlore phases （ Bi3Zn2Sb3O14 ） produce at about 700℃, and decompose to fine spinel phase （Zn7Sb2O12） when the temperature reaches to 900℃.This type of spinel phase makes ZnO crystal size minor. Also, the phase contained the Pr and different Pr oxides, which makes the whole material crystal size more uniform and compact. The fine structure improves the threshold voltage by about 60%, and modifies nonlinear coefficient of the ZnO material.展开更多
A technique for preparing perovskite type oxides was developed. By this technique, ultra fine particles of La 0.9 RE 0.1 MnO 3 (RE: Y, Ce, Pr, Sm, Gd,or Dy) with high surface area and single perovskite stru...A technique for preparing perovskite type oxides was developed. By this technique, ultra fine particles of La 0.9 RE 0.1 MnO 3 (RE: Y, Ce, Pr, Sm, Gd,or Dy) with high surface area and single perovskite structure were prepared, and the series of La 0.9 RE 0.1 MnO 3 catalysts were studied experimentally. The so prepared ultra fine particles exhibites high catalytic activity for CH 4 total oxidation. The ultra fine particles of La 0.9 RE 0.1 MnO 3 (except for La 0.9 Pr 0.1 MnO 3) prepared by this method are thermally much more stable than LaMnO 3. Of the La 0.9 RE 0.1 MnO 3 series, La 0.9 Y 0.1 MnO 3 is most thermally stable, and La 0.9 Y 0.1 MnO 3 or La 0.9 Gd 0.1 MnO 3 (varies with calcination temperature) exhibits the highest catalytic activity for total oxidation of methane. The specific surface area of La 0.9 Y 0.1 MnO 3 calcined at 1000 ℃ reaches 14.9 m 2·g -1 , while the specific surface area of LaMnO 3 calcined at the same temperature is only 1.8 m 2·g -1 .展开更多
文摘The doping effects of rare earth oxides Ho_2O_3 and Er_2O_3 on dielectric properties of BaTiO_3-based ceramics were studied. After adding rare earth elements, grain growth in this system was inhibited and the grain size was reduced evidently which realized the fine-grained effect. In this system, the trivalent oxides Ho_2O_3 and Er_2O_3 were added to BaTiO_3 ceramics. The rare earth oxides do not enter into inner lattice totally to replace A or B sites. Some of additives can improve dielectric strength by forming nonferroelectric phases, and the rest maintained at grain boundaries controls overgrowth of grains. The dielectric constant at room temperature is increased up to 3000 and the curve of TCC becomes flat. Meanwhile, the dielectric strength E_b becomes higher.
文摘The primariy application of rare - earth spin finishes on PET/PA composite super - fine denier fiber has been studied in this paper. It results in the improvement of fi-ber’s properties, such as increased whiteness, brightness and brilliance, effective and uniform spliting of compos-ite fiber into super - fine denier fiber and enhanced dye-ing effect.
基金Project supported by the National Natural Science Foundation of China (50474022 and 50574069 )
文摘Cerium carbonate powders were produced in a submerged circulation impinging stream reactor （SCISR） from Ce（NO3）3· 6H2O. NH4HCO3 was used as a precipitant in the reaction. Cerium carbonate powders were roasted to produce ultra-fine cerium dioxide （CeO2） powders. The optimal conditions of such production process were obtained by orthogonal and one-factor experiments. The results showed that ultra-fine and narrowly distributed cerium carbonate powders were produced under the optimal flowing conditions. The concentrations of Ce（NO3）3 and NH4HCO3 solutions were 02,5 and 0.3 mol · L^-1, respectively. The concentration of PEG4000 added in these two solutions was 4 g · L^-1. The stirring ratio, reaction temperature, feeding time, solution pH, reaction time and digestion time were 900 r · min^- 1,80 ℃, 20 min, 5 - 6, 5 min and 1 h, respectively. The final product, CeO2 powders, was obtained by roasting the produced cerium carbonate in air for 3 h at 500 ℃. The finally produced CeO2 powders were torispherical particles with a narrow size distribution of 0.8 -2.5 μm. The crystal structure of CeO2 powders belonged to cubic crystal system and its space point 5 group was OH^5-FM3M. Under optimal conditions, powders produced by SCISR were finer and more narrowly distributed than that by Stirred Tank Reactor （STR）.
文摘Ultra-fine CeO_2-ZrO_2 mixed oxide was successfully synthesized by wet-solid phase mechanochemical processing, Ce_2(CO_3)_3·8H_2O, ZrOCl_2·xH_2O and ammonia were used as reactants. It is found that the crystalline Ce_2(CO_3)_3·8H_2O and ZrOCl_2·xH_2O are changed to amorphous cerium and zirconium hydroxide precursor after milling with ammonia, and Ce_(0.15)Zr_(0.85)O_2 mixed oxide with pure tetragonal phase structure and medium particle size(D_(50))less than 1μm is formed by calcining precursor over 673 K. The XRD patterns indicate that the crystal unite size increases with rising calcining temperature due to crystal growth. However, the particle size and BET surface area of the Ce(Zr)O_2 mixed oxide decreases with rising calcining temperature, which may be attributed to the contract of particles and the vanish of holes inside grains.
基金Project supported by Rare Earth Department of National Development Committee Preparation of High Quality Polishing Powder
文摘Fine spherical particle sized ceria (CeO_2) was prepared by homogeneous precipitation method with ammonium bicarbonate as precipitant. The prepared CeO_2 has the primary particle size of 10～50 nm when calcined between 400～700 ℃ analyzed by XRD and the aggregated particle size is about 300 nm measured by LASER particle sizer. SEM, TG-DTA and Zeta-potential analyzer were employed individually to study the morphology and the formation of CeO_2 product. It was found that excess NH_4NO_3 can serve as an sphericallization agent to prepare spherical CeO_2 powder by precipitation method.
文摘The influence of Pr6O11 on the microstructure of ZnO varistors was researched. The results of experiment indicate that addition of Pr6O11 leads to the change of the formation process of the spinel phase. A lot of pyrochlore phases （ Bi3Zn2Sb3O14 ） produce at about 700℃, and decompose to fine spinel phase （Zn7Sb2O12） when the temperature reaches to 900℃.This type of spinel phase makes ZnO crystal size minor. Also, the phase contained the Pr and different Pr oxides, which makes the whole material crystal size more uniform and compact. The fine structure improves the threshold voltage by about 60%, and modifies nonlinear coefficient of the ZnO material.
文摘A technique for preparing perovskite type oxides was developed. By this technique, ultra fine particles of La 0.9 RE 0.1 MnO 3 (RE: Y, Ce, Pr, Sm, Gd,or Dy) with high surface area and single perovskite structure were prepared, and the series of La 0.9 RE 0.1 MnO 3 catalysts were studied experimentally. The so prepared ultra fine particles exhibites high catalytic activity for CH 4 total oxidation. The ultra fine particles of La 0.9 RE 0.1 MnO 3 (except for La 0.9 Pr 0.1 MnO 3) prepared by this method are thermally much more stable than LaMnO 3. Of the La 0.9 RE 0.1 MnO 3 series, La 0.9 Y 0.1 MnO 3 is most thermally stable, and La 0.9 Y 0.1 MnO 3 or La 0.9 Gd 0.1 MnO 3 (varies with calcination temperature) exhibits the highest catalytic activity for total oxidation of methane. The specific surface area of La 0.9 Y 0.1 MnO 3 calcined at 1000 ℃ reaches 14.9 m 2·g -1 , while the specific surface area of LaMnO 3 calcined at the same temperature is only 1.8 m 2·g -1 .
