共查询到20条相似文献,搜索用时 15 毫秒
1.
Huidong Li Wei-Heng Shih Wan Y. Shih 《International Journal of Applied Ceramic Technology》2009,6(2):205-215
The solution coating method is shown to provide more homogeneous mixing of the starting powders and purer (Na0.5 K0.5 )NbO3 (NKN) powder than the conventional method thereby rendering cold isostatic pressing unnecessary. Sintering NKN with potassium copper niobate (KCN) by uniaxial pressing gave a relative bulk density of 92%, d 33 coefficient of 112 pC/N and a loss factor of 1% after 6 h at 1100°C. In contrast, the conventional method yielded 84% relative bulk density and a 31% loss factor after 6 h at 1100°C and the sample was too porous to allow for dielectric and piezoelectric measurements. 相似文献
2.
An all-alkoxide route to films and nano-phase powders of the La0.5 Sr0.5 CoO3 perovskite is described. To our knowledge, this is the first purely alkoxide-based route to (La1− x Sr x )CoO3 , and it yields phase-pure and elementally homogeneous perovskite at 700°C by heating at 2°C/min. At 700°C, a cubic unit cell was obtained with a c =3.853Å, and after further heating to 1000°C, a rhombohedral cell could be indexed: a r =5.417 Å, αr =59.94°. Ninety to 130 nm thick films of La0.5 Sr0.5 CoO3 were obtained by spin coating. The gel-to-oxide conversion was studied in some detail, using thermo-gravimetric analysis, differential scanning calorimetry, powder X-ray diffraction, IR spectroscopy, and transmission electron microscope equipped with an energy-dispersive X-ray spectrometer. 相似文献
3.
Hwi-Yeol Park Joo-Young Choi Min-Kyu Choi Kyung-Hoon Cho Sahn Nahm Hyeung-Gyu Lee Hyung-Won Kang 《Journal of the American Ceramic Society》2008,91(7):2374-2377
When a small amount of CuO was added to (Na0.5 K0.5 )NbO3 (NKN) ceramics sintered at 960°C for 2 h, a dense microstructure with increased grains was developed, probably due to liquid-phase sintering. The Curie temperature slightly increased when CuO exceeded 1.5 mol%. The Cu2+ ion was considered to have replaced the Nb5+ ion and acted as a hardener, which increased the E c and Q m values of the NKN ceramics. High piezoelectric properties of k p =0.37, Q m =844, and ɛ3 T /ɛ0 =229 were obtained from the specimen containing 1.5 mol% of CuO sintered at 960°C for 2 h. 相似文献
4.
Ruzhong Zuo Jürgen Rödel Renzheng Chen Longtu Li 《Journal of the American Ceramic Society》2006,89(6):2010-2015
Lead-free Na0.5 K0.5 NbO3 (NKN) piezoelectric ceramics were fairly well densified at a relatively low temperature under atmospheric conditions. A relative density of 96%–99% can be achieved by either using high-energy attrition milling or adding 1 mol% oxide additives. It is suggested that ultra-fine starting powders by active milling or oxygen vacancies and even liquid phases from B-site oxide additives mainly lead to improved sintering. Not only were dielectric properties influenced by oxide additives, such as the Curie temperature ( T c ) and dielectric loss ( D ), but also the ferroelectricity was modified. A relatively large remanent polarization was produced, ranging from 16 μC/cm2 for pure NKN to 23 μC/cm2 for ZnO-added NKN samples. The following dielectric and piezoelectric properties were obtained: relative permittivity ɛ T 33 /ɛ 0 =570–650, planar mode electromechanical coupling factor, k p =32%–44%, and piezoelectric strain constant, d 33 =92–117 pC/N. 相似文献
5.
Hwi-Yeol Park In-Tae Seo Jae-Hong Choi Sahn Nahm Hyeung-Gyu Lee 《Journal of the American Ceramic Society》2010,93(1):36-39
(Na0.5 K0.5 )NbO3 (NKN) ceramic with 1.5 mol% CuO added (NKNC) was well sintered even at a low temperature of 900°C with the addition of ZnO. Most of the ZnO reacted with the CuO and formed the liquid phase that assisted the densification of the specimens at 900°C. A few Zn2+ ions entered the matrix of the specimens and increased the coercive field ( E c ) and Q m values of the specimens. High-piezoelectric properties of k p =0.37, Q m =755, and ɛ3 T /ɛ0 =327 were obtained from the NKNC ceramics containing 1.0 mol% ZnO sintered at 900°C for 2 h. 相似文献
6.
Pornsuda Bomlai Pattraporn Wichianrat Supasarute Muensit Steven J. Milne 《Journal of the American Ceramic Society》2007,90(5):1650-1655
Sodium-potassium niobate [Na0.5 K0.5 NbO3 ] powders were prepared following the conventional mixed oxide method. An orthorhombic XRD pattern, consistent with single-phase Na0.5 K0.5 NbO3 , was obtained after calcination at 900°C for 6 h. Introducing 5 mol% excess Na2 CO3 and K2 CO3 into the starting mixture allowed milder calcination conditions to be used, for example 800°C for 2 h. Primary particles in 5 mol% excess samples were cuboid, with maximum sizes of ∼2.5 μm. Equiaxed 0.3–0.4-μm particles were formed for non-excess powders, and also for powders prepared with 1 and 3 mol% excess alkali carbonates. The results suggest liquid formation during calcination of the excess 5-mol% starting powders. 相似文献
7.
Hiromichi Aono Mioko Tsuzaki Akihiro Kawaura Masatomi Sakamoto Enrico Traversa Yoshihiko Sadaoka 《Journal of the American Ceramic Society》2001,84(5):969-975
The heteronuclear LaMn(dhbaen)(OH)(NO3 )(H2 O)4 complex was synthesized and perovskite-type hexagonal LaMnO3 was obtained by its thermal decomposition at approximately 700°C. The complex and its decomposition products were analyzed using simultaneous thermogravimetric and differential thermal analysis (TG/DTA), X-ray diffraction (XRD) analysis, Fourier-transform infrared (FTIR) spectroscopy, Auger electron spectroscopy (AES), transmission electron microscopy (TEM) characterization, and specific surface area measurements. Although XRD analysis did not show the peaks of LaMnO3 for the sample sintered at 600°C, the presence of polycrystalline LaMnO3 together with an amorphous phase was confirmed by TEM-selected area diffraction. Particle sizes of the samples decomposed at 600° and 700°C were 20 and 50 nm, respectively. For the conventional solid-state reaction method, XRD results showed the formation of a LaMnO3 single phase for the samples fired above 1000°C. However, AES showed that the elemental distributions of La, Mn, and O on the surface were not homogeneous even for the sample sintered at 1200°C. The thermal decomposition of the heteronuclear complex at low temperatures allows the synthesis of single-phase hexagonal LaMnO3 powders having nanosized particles, homogeneous and free of intragranular pores, which are suitable for electroceramics applications. 相似文献
8.
Low-Temperature Crystallization of Sol-Gel Processed Pb0.5 Ba0.5 TiO3 : Powders and Oriented Thin Films
Suresh C. Pillai Stacey W. Boland Sossina M. Haile 《Journal of the American Ceramic Society》2004,87(7):1388-1391
A novel sol-gel process suitable for depositing thin-film lead barium titanate has been developed. X-ray diffraction analysis showed perovskite phase crystallization to occur at a temperature as low as 400°C with single-phase Pb0.5 Ba0.5 TiO3 (PBT) resulting at a temperature as low as 500°C. Small concentrations of barium carbonate were evident by X-ray diffraction at 400°C, and indications of minor, carbonate-containing phases were evident by FTIR at 600°C. Deposition of the sol by spin coating on single-crystal and thin-film MgO on silicon resulted in highly oriented PBT films after calcination at 600°C. Mixed (100)/(001) films were obtained on single-crystal MgO, whereas entirely (100) films were obtained on thin-film MgO. 相似文献
9.
Janez Bernard reja Benan Tadej Rojac Janez Holc Barbara Mali Marija Kosec 《Journal of the American Ceramic Society》2008,91(7):2409-2411
The objective of this work was to lower the sintering temperature of K0.5 Na0.5 NbO3 (KNN) without reducing its piezoelectric properties. The KNN was sintered using 0.5, 1, 2, and 4 mass% of (K, Na)-germanate. The influence of the novel sintering aid, based on alkaline germanate with a melting point near 700°C, on the sintering, density, and piezoelectric properties of KNN is presented. The alkaline-germanate-modified KNN ceramics reach up to 96% of theoretical density at sintering temperatures as low as 1000°C, which is approximately 100°C less than the sintering temperature of pure KNN. The relative dielectric permittivity (ɛ/ɛ0 ) and losses (tanδ), measured at 10 kHz, the piezo d 33 coefficient, the electromechanical coupling and mechanical quality factors ( k p , k t , Q m ) of KNN modified with 1 mass% of alkaline germanate are 397, 0.02, 120 pC/N, 0.40, 0.44, and 77, respectively. These values are comparable to the best values obtained for KNN ceramics sintered above 1100°C. 相似文献
10.
BaTi4 O9 and Ba2 Ti9 O20 precursors were prepared via a sol–gel method, using ethylenediaminetetraacetic acid as a chelating agent. The sol–gel precursors were heated at 700°–1200°C in air, and X-ray diffractometry (XRD) was used to determine the phase transformations as a function of temperature. Single-phase BaTi4 O9 could not be obtained, even after heating the precursors at 1200°C for 2 h, whereas single-phase Ba2 Ti9 O20 (as determined via XRD) was obtained at 1200°C for 2 h. Details of the synthesis and characterization of the resultant products have been given. 相似文献
11.
Zhijun Xu Ruiqing Chu Jigong Hao Guorong Li Qingrui Yin 《Journal of the American Ceramic Society》2008,91(3):910-913
SrBi4 Ti4 O15 (SBTi) powders were synthesized by a novel hybrid method of sol–gel and ultrasonic atomization. TiO2 particle was used as a starting material to replace other expensive soluble titanium salts. X-ray diffraction results showed that the pure-phase SBTi powders were obtained at 700°C for 2 h, which is much lower than the calcination temperature (800°–850°C) required in solid-state reactions. The ceramics sintered at 1100°C for 1 h exhibited 94.5% of relative density and a piezoelectric coefficient of 21 pC/N. The results showed that this hybrid method could lead to an attractive method for the industrial fabrication of SBTi materials. 相似文献
12.
Oleg A. Shlyakhtin Young-Jei Oh 《International Journal of Applied Ceramic Technology》2009,6(2):312-323
The liquid phase sintering of fine BiNbO4 powders allows to obtain dense ceramics with excellent microwave dielectric properties (ɛ=44–46; Q × f =16,500–21,600 GHz) at T ≥700°C. The thermal decomposition of freeze-dried precursors results in the crystallization of a metastable β'-BiNbO4 polymorph that transforms into a stable orthorhombic α-modification at T ≥700°C. The dependence of sinterability on the powder synthesis temperature shows the maximum at 600°C, corresponding to the formation of crystalline BiNbO4 powders with a grain size 80–100 nm. Sintering temperature reduction to 700°C prevents the deterioration of silver contacts during co-firing with BiNbO4 ceramics. In situ scanning electron microscopy observation of the morphological evolution during sintering shows that the intense shrinkage soon after the appearance of a CuO–V2 O5 eutectics-based liquid phase is accompanied by complete transformation of the ensemble of primary BiNbO4 particles. 相似文献
13.
Pure, single-phase stoichiometric Pb(Fe0.5 Nb0.5 )O3 (PFN) powders were successfully formed by molten salt synthesis using mixtures of NaCl and KCl salts. Lower temperatures and shorter times (1/2 h at 800°C) were needed for singlephase PFN formation from molten salts relative to those required for solid-phase methods (4 h at 1000°C). A systematic study indicating the effects of process parameters, such as temperature, time, and amount of flux with respect to starting oxides, on the PFN formation mechanism and its resulting powder characteristics is reported. The particle size increased with increasing synthesis temperature; the rate of increase was greatest above 900°C, which is close to the melting point of PbO. PFN powders formed by molten salt synthesis are spheroidal, free from aggregates, and sintered to good densities at temperatures as low as 1000°C. 相似文献
14.
La2 Ti2 O7 powders were prepared using three different techniques. Single-phase material was obtained at 1150°C by calcination of mixed oxides, at 1000°C by molten salt synthesis, and at 850°C by evaporative decomposition of solutions. Particle sizes and morphologies of the powders differed substantially, as did the sintered microstructures and dielectric properties. Very dense (99%), translucent, grain-oriented lanthanum titanate was fabricated by hot-forging at 1300°C under a 200-kg load. Anisotropy was demonstrated by X-ray diffraction, scanning electron microscopy, thermal expansion, and dielectric measurements. 相似文献
15.
Yu-Dong Hou Lei Hou Ting-Ting Zhang Man-Kang Zhu Hao Wang Hui Yan 《Journal of the American Ceramic Society》2007,90(6):1738-1743
The sol–gel–hydrothermal processing of (Na0.8 K0.2 )0.5 Bi0.5 TiO3 (NKBT) nanowires as well as their densification behavior were investigated. The morphology and structure analyses indicated that the sol–gel–hydrothermal route led to the formation of phase-pure perovskite NKBT nanowires with diameters of 50–80 nm and lengths of 1.5–2 μm, and the processing temperature was as low as 160°C, but the conventional sol–gel route tended to lead to the formation of NKBT agglomerated porous structured nanopowders, and the processing temperature was higher than 650°C. It is believed that the gel precursor and hydrothermal environment play an important role in the formation of the nanowires at a low temperature. Owing to the better packing efficiency and therefore a good sinterability of the freestanding nanowhiskers, the pressed pellets made by NKBT nanowires showed >98% theoretical density at 1100°C for 2 h. The sol–gel–hydrothermal-derived ceramics have typical characteristics of relaxor ferroelectrics, and the piezoelectric properties were better than the ceramics prepared by the conventional sol–gel and solid-state reaction. 相似文献
16.
Keqin Huang Man Feng John B. Goodenough 《Journal of the American Ceramic Society》1996,79(4):1100-1104
Sr- and Mg-doped LaGaO3 powders were prepared from a salt acetate solution. The stable solution was peptized by reacting ammonium hydroxide with the precursor solution. Thermal analysis (DTA/TGA) was used to characterize first the dehydration and then the thermal decomposition of the organic ligands of the dried gel. The transformation from amorphous powders into a crystallized, homogeneous oxide phase corresponds to two endothermic peaks in the DTA curve; the first one at 150°C is related to the removal of water and is followed by a shoulder at 250°C. The second peak at 300°C corresponds to a superposition of two decomposition reactions: acetate salt into its oxycarbonate and this oxycarbonate into its oxide. Two subsequent exothermic peaks correspond to oxidation of evolved gases such as methane, hydrogen, and carbon monoxide. TEM observations show an average 10 nm particle size of the LaGaO3 powder after annealing at 600°C. X-ray diffraction patterns indicate a pure primitive-cubic phase is formed by 1300°C without formation of any SrLaGaO3 impurity. The impedance spectroscopy on a 93%-dense sample exhibits no grain-boundary contribution and an ac conductivity σ= 0.11 Ω−1 ·cm−1 at 800°C. 相似文献
17.
Francesco Bozza Riccardo Polini Enrico Traversa 《Journal of the American Ceramic Society》2009,92(9):1999-2004
La0.8 Sr0.2 Ga0.8 Mg0.115 Co0.085 O3−δ (LSGMC) powders were prepared by polymeric precursor synthesis, using either polyvinyl alcohol (PVA) or citric acid (CA) as complexing agents. The powders were synthesized using different ratios between the complexing agent and the cations dissolved in solution. The obtained polymer gel precursors were dried and calcined at temperatures between 1000° and 1450°C. Single-phase LSGMC powders were obtained at a firing temperature of 1450°C, using PVA and a molar ratio between the hydroxylic groups and the total cations of 3:1. Phase-pure LSGMC powders were used to sinter (1490°C, 2 h) thick pellets. The functional properties of LSGMC pellets were assessed by electrochemical impedance spectroscopy. The electrical conductivity values and the apparent activation energies in different transport regimes were in agreement with literature data. The same LSGMC powders were deposited by electrophoretic deposition (EPD) on a green membrane containing lanthanum-doped ceria (La0.4 Ce0.6 O2− x , LDC), a binder, and carbon powders. The LSGMC/LDC bi-layer obtained by EPD was cofired at 1490°C for 2 h. A dense and crack-free 8-μm-thick LSGMC film supported on a porous skeleton of LDC was obtained. The combined use of proper powder synthesis and film processing routes has thus proven to be a viable way for manufacturing anode-supported LSGMC films. 相似文献
18.
Naitao Yang Xiaoyao Tan Zifeng Ma Alan Thursfield 《Journal of the American Ceramic Society》2009,92(11):2544-2550
Samaria-doped ceria (SDC, Ce0.8 Sm0.2 O1.9 ) ceramic powders of submicrometer size were synthesized by a sol–gel auto-combustion method. From these powders microtubes with a dual structure comprising of a dense layer and a porous substrate layer were fabricated in a single step through a phase inversion/sintering technique. A sintering temperature in excess of 1450°C is required for SDC to achieve gastight microtubes. The mechanical strength of the SDC microtubes increases with increasing sintering temperature and may attain up to 208 MPa when sintered at 1500°C. Electrical impedance spectroscopy studies indicate that the SDC microtubes have electrical conductivities of 4.46 × 10−4 –0.072 S/cm and corresponding activation energy of 81.9 kJ/mol at temperatures between 400° and 800°C. Full fuel cells were fabricated by coating Ba0.5 Sr0.5 Co0.8 Fe0.2 O3−δ (BSCF) on to the inner surface and a Ni-SDC cermet on to the outer surface of the gastight microtubes to act as the cathode and the anode, respectively. The resultant BSCF|SDC|Ni-SDC microcells have a stable output maximum of 106 mW/cm2 at 750°C when hydrogen and air were used as fuel and oxidant gas, respectively. 相似文献
19.
Equilibrium partial pressures of SiF4 were measured for the reactions 2SiO2 ( c )+2BeF2 ( d )⇋SiF4 ( g )+Be2 SiO4 ( c ) (log P siF4 (mm) = [8.790 - 7620/ T ] ±0.06(500°–640°C)) and Be2 SiO4 ( c ) +2BeF2 ( d )⇋SiF4 ( g ) +4BeO( c )(log P siF4 (mm) = [9.530–9400/T] ±0.04 (700°–780°C)), wherein BeF2 was present in solution with LiF as molten Li2 BeF4 . The solubility of SiF4 was low (∼0.04 mol kg-1 atm-1 ) in the melt. The results for the first equilibrium were combined with available thermochemical data to calculate improved Δ Hf and Δ Gf values for phenacite (–497.57 ±2.2 and –470.22±2.2 kcal, respectively, at 298°K). The few measurements above 700°C for the second equilibrium are consistent with the temperature of the subsolidus decomposition of phenacite to BeO and SiO2 and with the heat of this decomposition as determined by Holm and Kleppa. Below 700°C, the pressures of SiF4 generated showed an increasing positive deviation from the expression given for the equilibrium involving Be2 SiO4 and BeO. This deviation might have been caused by the formation of an unidentified phase below 700°C which replaced the BeO; it more likely resulted from a metastable equilibrium involving BeO and SiO2 . 相似文献
20.
Ruzhong Zuo Xusheng Fang Chun Ye Longtu Li 《Journal of the American Ceramic Society》2007,90(8):2424-2428
(1− x )(Na0.5 K0.5 )NbO3 –(Bi0.5 K0.5 )TiO3 solid solution ceramics were successfully fabricated, exhibiting a continuous phase transition with changing x at room temperature from orthorhombic, to tetragonal, to cubic, and finally to tetragonal symmetries. A morphotropic phase boundary (MPB) between orthorhombic and tetragonal ferroelectric phases was found at 2–3 mol% (Bi0.5 K0.5 )TiO3 (BKT), which brings about enhanced piezoelectric and electromechanical properties of piezoelectric constant d 33 =192 pC/N and planar electromechanical coupling coefficient k p =45%. The MPB composition has a Curie temperature of 370°–380°C, comparable with that of the widely used PZT materials. These results demonstrate that this system is a promising lead-free piezoelectric candidate material. 相似文献