共查询到20条相似文献,搜索用时 31 毫秒
1.
Debao Zhang Baoyu Chen Zhuping Liu Shunguang Li Lili Hu 《Journal of the American Ceramic Society》2004,87(12):2228-2231
Er3+ -doped sodium lanthanum aluminosilicate glasses with compositions of (90− x )(0.7SiO2 ·0.3Al2 O3 )· x Na2 O·8.2La2 O3 · 0.6Er2 O3 ·0.2Yb2 O3 ·1Sb2 O3 (in mol%) ( x = 12, 20, 24, 40, 60 mol%) were prepared and their spectroscopic properties were investigated. Judd–Ofelt analysis was used to calculate spectroscopic properties of all glasses. The Judd–Ofelt intensity parameter Ω t ( t = 2, 4, 6) decreases with increasing Na2 O. Ω2 decreases rapidly with increasing Na2 O while Ω4 and Ω6 decrease slowly. Both the fluorescent lifetime and the radiative transition rate increase with increasing Na2 O. Fluorescence spectra of the 4 I 13/2 to 4 I 15/2 transition have been measured and the change with Na2 O content is discussed. It is found that the full width at half-maximum decreases with increasing Na2 O. 相似文献
2.
Junying Zhang Zhongtai Zhang Zilong Tang Yuanhua Lin 《Journal of the American Ceramic Society》2002,85(4):998-1000
A (Ce0.67 Tb0.33 )Mn x Mg1− x Al11 O19 phosphor powder was synthesized, using a simple sol–gel process, by mixing citric acid with CeO2 , Tb4 O7 , Al(NO3 )3 ·9H2 O, Mg(OH)2 ·4MgCO3 ·6H2 O, and Mn(CH3 COO)2 . The phosphor crystallized completely at 1200°C, and the phosphor particle size was between 1 and 5 μm. The excitation spectrum was characteristic of Ce3+ , while the emission spectrum was composed of lines from Tb3+ and Mn2+ . The Mn2+ gave a green fluorescence band, and concentration quenching occurred when x > 0.10. The luminescent properties of the phosphor were explained by a configurational coordinate model. 相似文献
3.
The phase diagram for the ternary system MgO─P2 O5 ─H2 O at 25°C has been constructed. The magnesium phosphates represented are Mg(H2 PO4 )2 · n H2 O ( n = 4, 2, 0), MgHPO4 ·3H2 O, and Mg3 (PO4 )2 · m H2 O ( m = 8, 22). Because of the large differences in the solubilities of these compounds, the technique which involves plotting the mole fractions of MgO and P2 O5 as their 10th roots has been employed. With the exception of MgHPO4 ·3H2 O, the magnesium phosphates are incongruently soluble. Because incongruency is associated with a peritectic-like reaction, the phase Mg2 (PO4 )3 · 8H2 O persists metastably for an extended period. 相似文献
4.
A narrow region of Zn-vacancy-containing cubic perovskites was formed in the (1− x )Ba3 (ZnNb2 )O9 −( x )Ba3 W2 O9 system up to 2 mol% substitution ( x =0.02). The introduction of cation vacancies enhanced the stability of the 1:2 B-site ordered form of the structure, Ba(Zn1− x □ x )1/3 (Nb1− x W x )2/3 O3 , which underwent an order–disorder transition at 1410°C, ∼35° higher than pure Ba(Zn1/3 Nb2/3 )O3 . The Zn vacancies also accelerated the kinetics of the ordering reaction, and samples with x =0.006 comprised large ordered domains with a high lattice distortion ( c/a =1.226) after a 12 h anneal at 1300°C. The tungstate-containing solid solutions can be sintered to a high density at 1390°C, and the resultant ordered ceramics exhibit some of the highest microwave dielectric Q factors ( Q × f =1 18 000 at 8 GHz) reported for a niobate-based perovskite. 相似文献
5.
Masaru Yoshinaka Ken Hirota Masayuki Ito Hiroshi Takano Osamu Yamaguchi 《Journal of the American Ceramic Society》1999,82(1):216-218
Tin(IV) oxide (SnO2 ) crystallizes at room temperature by adding hydrazine monohydrate ((NH2 )2 · H2 O) to a hydrochloric acid solution of tin, followed by washing and drying. Well-densified SnO2 ceramics (99.8% of theoretical) with an average grain size of 0.9 μm have been fabricated by hot isostatic pressing for 2 h at 900°C and 196 MPa. Their Vickers hardness and bending strength are 14.4 GPa and 200 MPa, respectively. They exhibit an electrical conductivity of 2 × 10−3 −9 × 10−3 S·cm−1 at room temperature. 相似文献
6.
Marin Cernea Elena Chirtop Dana Neacsu Iuliana Pasuk Sergiu Iordanescu 《Journal of the American Ceramic Society》2002,85(2):499-503
A barium titanate precursor with a barium:titanium ratio of 1:4 was prepared by controlled coprecipitation of mixed barium and titanium species with an ammonium oxalate aqueous solution at pH 7. The results of thermal analysis and IR measurement show that the obtained precursor is a mixture of BaC2 O4 ·0.5H2 O and TiO(OH)2 ·1.5H2 O in a molar ratio of 1:4. Crystallized BaTi4 O9 was obtained by the thermal decomposition of a precipitate precursor at 1300°C for 2 h in air. The dimensions of the powder calcined at 1000°C are between 100 and 300 nm. The grain dimensions of the sintered sample for 2 h at 1300°C are of the order of 10 to 30 μm. Dielectric properties of disk-shaped sintered specimens in the microwave frequency region were measured using the TE011 mode. Excellent microwave characteristics for BaTi4 O9 —ɛ= 38 ± 0.5, Q = 3800–4000 at 6–7 GHz and τ f = 11 ± 0.7 ppm/°C—were found. 相似文献
7.
The phase relations were established experimentally for the system CaO-Al2 O3 -P2 O5 -H2 O at 200°C and 1710 kPa. The quaternary compound, crandallite, CaAl3 (PO4 )2 (OH)5 · H2 O, was found to be stable. Compatibility joins in the system were determined. The phase relations are presented on the isothermal-isobaric 90 wt% water plane and by projecting the primary fields of the liquidus surface onto the same plane. 相似文献
8.
Rejini Rajamma Mailadil Thomas Sebastian 《Journal of the American Ceramic Society》2007,90(8):2472-2475
The microwave dielectric properties of two A-site-deficient perovskite-type ceramics in the La6 Mg4 A2 W2 O24 [A=Ta and Nb] system were investigated. The compounds were synthesized by the solid-state ceramic route. The structure and microstructure were analyzed using X-ray diffraction and scanning electron microscopy techniques. The dielectric properties were measured in the microwave frequency range [4–6 GHz] by the resonance method. La6 Mg4 Ta2 W2 O24 had Q u × f =13 600 GHz, ɛr =25.2, and τf =−45 ppm/°C and La6 Mg4 Nb2 W2 O24 had Q u × f =16 400 GHz, ɛr =25.8, and τf =−56 ppm/°C. 相似文献
9.
Phase stability, sinterability, and microwave dielectric properties of Bi2 W2 O9 ceramics and their cofireability with Ag, Cu, and Au electrodes have been investigated. Single-phase Bi2 W2 O9 powder was synthesized by solid-state reaction in air at 800°C for 3 days. X-ray powder diffraction data show Bi2 W2 O9 to have an orthorhombic crystal structure described by the noncentrosymmetric space group Pna 21 , with lattice parameters a =5.4401(8), b =5.4191(8), c =23.713(4) Å. Ceramics fired at temperatures up to 865°C remain single-phase but above this temperature ferroelectric Bi2 WO6 appears as a secondary phase. The measured relative permittivity of Bi2 W2 O9 ceramics increases continuously from 28.6 to 40.7 for compacts fired between 860° and 885°C. The bulk relative permittivity of Bi2 W2 O9 corrected for porosity was calculated as 41.3. Bi2 W2 O9 ceramics fired up to 875°C exhibit moderate quality factors, Q × f r , ∼7500–7700 GHz and negative temperature coefficient of resonant frequency, ∼−54 to −63 ppm/°C. Chemical compatibility experiments show Bi2 W2 O9 ceramics to react with both Ag and Cu electrodes, but to form good contacts with Au electrodes. 相似文献
10.
Rutile or anatase may be depolymerized and complexed by sequential treatment with (i) H2 SO4 /(NH4 )2 SO4 , (ii) H2 O, and (iii) catechol/NH4 OH to produce the intermediate (NH4 )2 (Ti(catecholate)3 ) · 2H2 O. Treatment with Ba(OH)2 · 8H2 O leads to an acid-base reaction generating Ba(Ti(catecholate)3 ) · 3H2 O, in which the Ba:Ti ratio is held at 1:1 at the molecular level. Calcination produces BaTiO3 powder. 相似文献
11.
Monika Agarwal Mark R. de Guire Arthur H. Heuer 《Journal of the American Ceramic Society》1997,80(12):2967-2981
Undoped or Y2 O3 -doped ZrO2 thin films were deposited on self-assembled monolayers (SAMs) with either sulfonate or methyl terminal functionalities on single-crystal silicon substrates. The undoped films were formed by enhanced hydrolysis of zirconium sulfate (Zr(SO4 )·4H4 O) solutions in the presence of HCl at 70°C. Typically, these films were a mixture of two phases: nanocrystalline tetragonal- ( t -) ZrO2 and an amorphous basic zirconium sulfate. However, films with little or no amorphous material could be produced. The mechanism of film formation and the growth kinetics have been explained through a coagulation model involving homogeneous nucleation, particle adhesion, and aggregation onto the substrate. Annealing of these films at 500°C led to complete crystallization to t -ZrO2 . Amorphous Y2 O3 -containing ZrO2 films were prepared from a precursor solution containing zirconium sulfate, yttrium sulfate (Y2 (SO4 )3 8·H2 O), and urea (NH2 CONH2 ) at pH 2.2–3.0 at 80°C. These films also were fully crystalline after annealing at 500°C. 相似文献
12.
The precursor [NH4 ]2 [Ti(catecholate)3 ] · 2H2 O is known to react with Ba(OH)2 · 8H2 O in an acid/base process that generates Ba[Ti(catecholate)3 ] · 3H2 O, a compound which undergoes low-temperatue calcination to produce BaTiO3 powder. Attempts to develop similar routes to PbTiO3 have been frustrated, since lead(II) hydroxide does not exist. The amphoteric yellow PbO and the basic oxide, Pb6 O(OH)6 4+ , are both insufficiently basic to react with [NH4 ]2 [Ti(catecholate)3 ] · 2H2 O. Based on the large sizes of both the [Ti(catecholate)3 ]2- anion and the Pb2+ cation, a precipitation method has been developed in which lead nitrate and [NH4 ]2 [Ti(catecholate)3 ] · 2H2 O are added together in an aqueous medium causing precipitation and leaving only NH4 NO3 in solution. The lead-titanium-catecholate complex that forms in this manner undergoes low-temperature pyrolysis to produce PbTiO3 . SEM indicates a submicrometer ultimate crystallite size. 相似文献
13.
Phase equilibria have been determined in the system CaO-Al2 O3 -H2 O in the temperature range 100° to 1000°C. under water pressures of up to 3000 atmospheres. Only three hydrated phases are formed stably in the system: Ca(OH)2 , 3CaO·Al2 O3 ·6H2 O, and 4CaO·3Al2 O3 -3H2 O. Pressure-temperature curves delineating the equilibrium decomposition of each of these phases have been determined, and some ther-mochemical data have been deduced therefrom. It has been established that both the compounds CaO·Al2 O3 and 3CaO·Al2 O3 have a minimum temperature of stability which is above 1000°C. The relevance of the new data to some aspects of cement chemistry is discussed. 相似文献
14.
P. K. GALLAGHER D. W. JOHNSON JR. E. M. VOGEL 《Journal of the American Ceramic Society》1977,60(1-2):28-31
Samples of LaMn1-x Cux O3-y in the range 0≤x≤0.8 were prepared from freeze-dried solutions of the nitrates. Samples with x≤0.6 were single-phase perovskites. At higher values of x , the samples contained La2 CuO4 and CuO as well as the perovskite phase. Samples of LaMn1−x ,Cux ,O3−y supported on ceramic monoliths or when mixed with powdered A12 O3 exhibit catalytic activity for the oxidation of CO. Greatest activity is shown for 0.4≤x≤0.7. Although the catalysts are severely poisoned by SO2 , 2% H2 O in the gas stream causes only slight deactivation. Activities of other oxide catalysts were also measured and compared. Rate constants per unit surface area at 200° to 400°C follow the order Co3 O4 >Pt>LaMn1−x Cux O3−y (0.4≤x≤0.7)>copper chromite>La1−x Srx ,MnO3 ≤ other substituted LaMnO3 materials, CuO, or La2 CuO4 . The perovskite catalyst is more stable than Co3 O4 or copper chromite when heated in 10% H2 + 90% N2 . 相似文献
15.
Ji-Guang Li Takayasu Ikegami Toshiyuki Mori Yoshiyuki Yajima 《Journal of the American Ceramic Society》2004,87(6):1008-1013
Hydroxyl-type Sc2 O3 precursors have been synthesized via precipitation at 80°C with hexamethylenetetramine as the precipitant. The effects of starting salts (scandium nitrate and sulfate) on powder properties are investigated. Characterizations of the powders are achieved by elemental analysis, X-ray diffractometry (XRD), differential thermal analysis/thermogravimetry (DTA/TG), high-resolution scanning electron microscopy (HRSEM), and Brunauer-Emmett-Teller (BET) analysis. Hard-aggregated precursors (γ-ScOOH·0.6H2 O) are formed with scandium nitrate, which convert to Sc2 O3 at temperatures ≥400°C, yielding nanocrystalline oxides of low surface area. The use of sulfate leads to a loosely agglomerated basic sulfate powder having an approximate composition of Sc(OH)2.6 (SO4 )0.2 ·H2 O. The powder transforms to Sc2 O3 via dehydroxylization and desulfurization at temperatures up to 1000°C. Well-dispersed Sc2 O3 nanopowders (∼64.3 nm) of high purity have been obtained by calcining the basic sulfate at 1000°C for 4 h. The effects of SO4 2− on powder properties are discussed. 相似文献
16.
Phase relations in the system Bi2 O3 -WO3 were studied from 500° to 1100°C. Four intermediate phases, 7Bi2 O3 · WO3 , 7Bi2 O3 · 2WO3 , Bi2 O3 · WO3 , and Bi2 O3 · 2WO3 , were found. The 7B2 O · WO3 phase is tetragonal with a 0 = 5.52 Å and c 0 = 17.39 Å and transforms to the fcc structure at 784°C; 7Bi2 O3 · 2WO3 has the fcc structure and forms an extensive range of solid solutions in the system. Both Bi2 O3 · WO3 and Bi2 O3 · 2WO3 are orthorhombic with (in Å) a 0 = 5.45, b 0 =5.46, c 0 = 16.42 and a 0 = 5.42, b 0 = 5.41, c 0 = 23.7, respectively. Two eutectic points and one peritectic exist in the system at, respectively, 905°± 3°C and 64 mol% WO3 , 907°± 3°C and 70 mol% WO3 , and 965°± 5°C and 10 mol% WO3 . 相似文献
17.
Seiji Shinohara Jong-Gab Baek Tetsuhiko Isobe Mamoru Senna 《Journal of the American Ceramic Society》2000,83(12):3208-3210
Phase-pure perovskite Pb(Zn x Mg1– x )1/3 Nb2/3 O3 solid solution (PZ x M1– x N) is obtained for x ≦ 0.7 by heating a milled stoichiometric mixture of PbO, Mg(OH)2 , Nb2 O5 , and 2ZnCO3 ·3Zn(OH)2 ·H2 O at 1100°C for 1 h. Percent perovskite ( f P ) with respect to total crystalline phase decreases with increasing temperature of subsequent heating then increases to 900°C for the mixtures where x ≦ 0.8 and milled for 3 h. For mixtures with x = 0.9 and x = 1, f P decreases monotonically. Curie temperature increases almost linearly with increasing x up to x = 0.7. The maximum dielectric constant at 1 kHz is 2×104 and 1.7×104 for the mixture with x = 0.4 and x = 0.7, respectively. The stabilization mechanism of strained perovskite is discussed. 相似文献
18.
Qiwei Chen Ying Shi Liqiong An Jiyang Chen Jianlin Shi 《Journal of the American Ceramic Society》2006,89(6):2038-2042
A novel co-precipitation process was adopted for the preparation of highly sinterable europium-doped lutetia powders using ammonium hydroxide (NH3 ·H2 O) and ammonium hydrogen carbonate (NH4 HCO3 ) as the mixed precipitant. The resultant powders calcined at 1000°C for 2 h showed good dispersity and excellent sinterability. Highly transparent polycrystalline lutetia ceramics with a relative density of ∼99.9% were fabricated by pressureless sintering in flowing H2 atmosphere at 1850°C for 6 h without any additives. The average grain sizes of the transparent material were estimated to be 50–60 μm. Optical in-line transmittance in the visible wavelength region for Lu2 O3 ceramics (1 mm in thickness) reached 80%. The luminescence and decay behavior of the obtained transparent plate and the corresponding nanophosphors were also investigated. 相似文献
19.
Ji-Guang Li Takayasu Ikegami Toshiyuki Mori 《Journal of the American Ceramic Society》2005,88(4):817-821
We report here the fabrication of transparent Sc2 O3 ceramics via vacuum sintering. The starting Sc2 O3 powders are pyrolyzed from a basic sulfate precursor (Sc(OH)2.6 (SO4 )0.2 ·H2 O) precipitated from scandium sulfate solution with hexamethylenetetramine as the precipitant. Thermal decomposition behavior of the precursor is studied via differential thermal analysis/thermogravimetry, Fourier transform infrared spectroscopy, X-ray diffractometry, and elemental analysis. Sinterability of the Sc2 O3 powders is studied via dilatometry. Microstructure evolution of the ceramic during sintering is investigated via field emission scanning electron microscopy. The best calcination temperature for the precursor is 1100°C, at which the resultant Sc2 O3 powder is ultrafine (∼85 nm), well dispersed, and almost free from residual sulfur contamination. With this reactive powder, transparent Sc2 O3 ceramics having an average grain size of ∼9 μm and showing a visible wavelength transmittance of ∼60–62% (∼76% of that of Sc2 O3 single crystal) have been fabricated via vacuum sintering at a relatively low temperature of 1700°C for 4 h. 相似文献
20.
The composition and lattice parameters of co-precipitated (La0.3 Y0.7 ) orthophosphate were studied using X-ray diffraction (XRD), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX). The results indicate that the as-precipitated powder consists of single-phase (La0.3 Y0.7 PO4 ·H2 O) rhabdophane nanoparticles. Heat treatment at 950°C caused the decomposition of rhabdophane into a (La1− x Y x )PO4 monazite solid solution and YPO4 xenotime. The solid solubility of Y in LaPO4 monazite from 1000° to 1600°C was studied using XRD, TEM, and EDX. The implications of the findings for controlling the coefficient of thermal expansion of the prospective two-phase monazite–xenotime fiber coatings for ceramic composites applications are discussed. 相似文献