共查询到20条相似文献,搜索用时 31 毫秒
1.
Takeshi Shiono Koji Shiono Kazuyo Miyamoto Giuseppe Pezzotti 《Journal of the American Ceramic Society》2000,83(1):235-37
A precursor was synthesized from a heterogeneous alkoxide solution that contained fine MgO powder, which allowed the preparation of MgAl2 O4 spinel powder with high sinterability characteristics. The precursor consisted of a mixture of boehmite (AlO(OH)) and a mixed hydroxide (Mg4 Al2 (OH)14 · 3H2 O). The spinel phase formed through two steps: (i) decomposition of the mixed hydroxide at low temperature and (ii) solid-state reaction between MgO and γ-Al2 O3 at higher temperatures. Dense polycrystalline spinel could be obtained from the calcined powders at sintering temperatures as low as 1400°C. 相似文献
2.
Nanosized ZnO particles are successfully synthesized via mechanical activation of a zinc nitrate hydroxide hydrate (Zn5 (NO3 )2 (OH)8 ·2H2 O) precursor in NaCl matrix for 15 h. The ZnO particles obtained are in the nanosize range of ∼20 nm, with a well-established hexagonal morphology. They compare favorably with those derived from conventional calcination of the precursor. The decomposition of Zn5 (NO3 )2 (OH)8 ·2H2 O precursor and formation of nanocrystalline ZnO cannot be completed by mechanical activation in the absence of NaCl, which acts as both an effective dispersing matrix and drying agent although it remains chemically inert during mechanical activation. The powder derived from calcination at 400°C does not possess powder characteristics comparable to that of the powder derived from the mechanical activation in NaCl, because of the extensive particle coarsening and aggregation at the calcination temperature. 相似文献
3.
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
4.
Synthesis of Mesoporous Needle-Shaped Ytterbium Oxide Crystals by Solvothermal Treatment of Ytterbium Chloride 总被引:1,自引:0,他引:1
Saburo Hosokawa Shinji Iwamoto Masashi Inoue 《Journal of the American Ceramic Society》2007,90(4):1215-1221
The reaction of rare-earth (RE; Y, Er, and Yb) chloride hydrates in 1,4-butanediol at 300°C for 2 h gave mixtures of RE(OH)2 Cl and RE2 O3 · x H2 O, and the products were composed of irregularly shaped particles. A prolonged reaction (10 h) yielded a mixture of RE(OH)2 Cl and RE2 O3 · x H2 O for Er or Y, but phase-pure RE2 O3 · x H2 O was obtained for Yb. The product for Yb comprised needle-shaped single crystals of Yb2 O3 · x H2 O with a width of 0.2–0.6 μm and a length of 5–15 μm. The Yb2 O3 · x H2 O phase decomposed to Yb2 O3 at 350°–500°C, preserving the needle-shaped morphology; this was maintained even after calcination at 1100°C. Single crystals of Yb2 O3 obtained by the calcination of Yb2 O3 · x H2 O at 500°C had very small voids and the voids were enlarged to 35 Å in diameter by calcination at 800°C. 相似文献
5.
Low-Temperature Fabrication of Transparent Yttrium Aluminum Garnet (YAG) Ceramics without Additives 总被引:12,自引:0,他引:12
Ji-Guang Li Takayasu Ikegami Jong-Heun Lee Toshiyuki Mori 《Journal of the American Ceramic Society》2000,83(4):961-963
A carbonate precursor of yttrium aluminum garnet (YAG) with an approximate composition of NH4 AlY0.6 (CO3 )1.9 (OH)2 ·0.9H2 O was synthesized via a coprecipitation method from a mixed solution of ammonium aluminum sulfate and yttrium nitrate, using ammonium hydrogen carbonate as the precipitant. The precursor precipitate was characterized using chemical analysis, differential thermal analysis/thermogravimetry, X-ray diffractometry, and scanning electron microscopy. The sinterability of the YAG powders was evaluated by sintering at a constant rate of heating in air and vacuum sintering. The results showed that the precursor completely transforms to YAG at ∼1000°C via the formation of a yttrium aluminate perovskite (YAP) phase. YAG powders obtained by calcining the precursor at temperatures of ≤1200°C were highly sinterable and could be densified to transparency under vacuum at 1700°C in 1 h without additives. 相似文献
6.
Axel Nørlund Christensen Torben R. Jensen Nicola V. Y. Scarlett Ian C. Madsen Jonathan C. Hanson 《Journal of the American Ceramic Society》2004,87(8):1488-1493
The hydrolysis of pure and sodium-substituted calcium aluminates and cement clinker phases was investigated in situ in the temperature range 25°–170°C, using the angle dispersive powder synchrotron powder X-ray diffraction technique. The final hydrolysis product in all cases was Ca3 Al2 (OH)12 . The intermediate phase Ca4 Al2 O7 ·19H2 O was formed from the pure calcium aluminates, and the intermediate phases Ca4 Al2 O7 · x H2 O, x = 11, 13, or 19, were formed from the cement clinker phases. 相似文献
7.
Qingmei Lu Wensheng Dong Haojing Wang Xinkui Wang 《Journal of the American Ceramic Society》2002,85(2):490-492
Yttrium aluminum garnet (YAG, Y3 Al5 O12 ) was synthesized by sol–gel processing from the stoichiometric amounts of aluminum pellets, Y(NO3 )3 ·6H2 O, and Al(NO3 )3 ·9H2 O or AlCl3 ·6H2 O, with suitable kinds of acid (citric acid, acetic acid, etc.) as catalysts. Polycrystalline YAG powder was obtained by drying the YAG precursor followed by calcination at temperatures above 900°C. Thermogravimetry/differential thermal analysis and Fourier transform infrared specotrscopic analyses in air showed an exothermic peak at ∼900°C, attributed to the formation of a polycrystalline YAG phase and weight loss of 60% at 1000°C, caused by the decomposition of hydroxyl and NO3 − , etc. X-ray diffraction analysis showed that YAG can be formed at 900°C, and no other intermediate was observed. In particular, the YAG sol can be used for dry-spinning fibers with the aid of some organic polymer. 相似文献
8.
Monoclinic hydrous-zirconia fine particles that contained cerium(IV) hydroxide (Ce(OH)4 ) were heated from 200°C to 600°C, to investigate the phase transformation to CeO2 -doped tetragonal ZrO2 . Both ZrOCl2 ·8H2 O and CeCl3 ·7H2 O were dissolved in aqueous solutions and then boiled to prepare the hydrous-zirconia particles. The Ce(OH)4 -containing hydrous-zirconia particles were prepared by adding aqueous ammonia into the boiled solutions. The monoclinic-to-tetragonal ( m right arrow t ) phase transformation of the Ce(OH)4 -containing hydrous zirconias was observed at 300°C using X-ray diffraction (XRD). XRD and Brunauer-Emmett-Teller (BET) specific surface area measurements revealed that the Ce(OH)4 -containing hydrous zirconias had a tendency to transform from the monoclinic phase to the tetragonal phase at lower temperatures as the primary particle size of the hydrous zirconia decreased and the Ce(OH)4 content increased. These tendencies for the m right arrow t phase transformation agree with the conclusions that have been derived from thermodynamic and kinetic considerations. 相似文献
9.
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
10.
Ping-Hua Xiang Xian-Lin Dong Chu-De Feng Yong-Ling Wang 《Journal of the American Ceramic Society》2003,86(9):1631-1634
NiO nanoparticle-coated lead zirconate titanate (PZT) powders are successfully fabricated by the heterogeneous precipitation method using PZT, Ni(NO3 )2 ·6H2 O, and NH4 HCO3 as the starting materials. The amorphous NiCO3 ·2Ni(OH)2 ·2H2 O are uniformly coated on the surface of PZT particles. XRD analysis and the selected-area diffraction (SAD) pattern indicate that the amorphous coating layer is crystallized to NiO after being calcined at 400°C for 2 h. TEM images show that the NiO particles of ∼8 nm are spherical and weakly agglomerated. The thickness of the nanocrystalline NiO coating layer on the surface of PZT particle is ∼30 nm. 相似文献
11.
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
12.
Reactive Ceria Nanopowders via Carbonate Precipitation 总被引:3,自引:0,他引:3
Ji-Guang Li Takayasu Ikegami Yarong Wang Toshiyuki Mori 《Journal of the American Ceramic Society》2002,85(9):2376-2378
Nanocrystalline CeO2 powders have been successfully synthesized via a carbonate precipitation method, using ammonium carbonate (AC) as the precipitant and cerium nitrate hexahydrate as the cerium source. The AC/Ce3+ molar ratio ( R ) affects significantly precursor properties, and spherical nanoparticles can be produced only in a narrow range of 2 < R ≤ 3. The precursor, having an approximate composition of Ce(OH)CO3 ·2.5H2 O, decomposes to CeO2 at temperatures ≥300°C. The CeO2 powder calcined at 700°C exhibits high reactivity and can be densified to >99% of theoretical at 1000°C. 相似文献
13.
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
14.
Preparation of Ultra-Fine Nickel Manganite Powders and Ceramics by a Solid-State Coordination Reaction 总被引:2,自引:0,他引:2
Dao-lai Fang Zhong-bing Wang Ping-hua Yang Wei Liu Chu-sheng Chen A. J. A. Winnubst 《Journal of the American Ceramic Society》2006,89(1):230-235
A solid-state coordination reaction was adopted to prepare negative temperature coefficient ceramics. A mixed oxalate NiMn2 (C2 O4 )3 ·6H2 O, a coordination compound, was synthesized by milling a mixture of nickel acetate, manganese acetate, and oxalic acid for 5 h at room temperature. An ultrafine NiMn2 O4 powder was obtained by calcining the mixed oxalate in air at 850°C for 2 h. Ceramics with a relative density of more than 97% were achieved by sintering powder compacts at a temperature as low as 1050°C for 5 h. The specific electrical resistivity ρ25°C and the thermal constant B 25°/85°C were 2174 Ω·cm and 3884 K, respectively. The drift of the resistivity after aging at 150°C for 1000 h was 3.0%. 相似文献
15.
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
16.
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
17.
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
18.
Zhi-Zhan Chen Er-Wei Shi Yan-Qing Zheng Wen-Jun Li Bing Xiao Ji-Yong Zhuang Lian-An Tang 《Journal of the American Ceramic Society》2005,88(1):127-133
Zinc aluminate (ZnAl2 O4 ) particles have been synthesized by the hydrothermal method using NH3 ·H2 O as a pH adjustment mineralizer. Experimental results showed that ZnAl2 O4 particle size was dependent on the precursor pH, and could be controlled through pH adjustment. It was 5.5, 11.5, and 27 nm when the precursor pH was 8.2, 9.3, and 10.5, respectively. On the other hand, the particle size distribution changed broader with increase in pH. These differences were attributable to the different NH3 ·H2 O function. NH3 ·H2 O was mainly used as a base at lower pH (<9.0), while its complex function predominated at higher one (>9.5). From thermodynamic viewpoint, the rate-limiting steps were dissolution of Al(OH)3 and γ-AlO(OH) to Al(OH)4 − at lower and higher pH, respectively. The newly formed γ-AlO(OH) with high reactivity was the critical factor in the synthesis of bimodal particles. Higher temperature treatment of γ-AlO(OH) could decrease the reactivity, and could be used as an aluminum source for synthesis uniform ZnAl2 O4 particles. 相似文献
19.
In this communication, we describe an inexpensive and feasible method for the preparation of hexagonal boron nitride (h–BN) nanorods in the absence of metal catalyst. Tertiary calcium phosphate (Ca3 (PO4 )2 ) and ammonium biborate hydrate (NH4 HB4 O7 ·3H2 O) were selected as starting materials where calcium phosphate was used as a diluting agent to prevent the formation of bulk B2 O3 during the thermolysis of ammonium biborate hydrate. The mixture was nitrided at 900°C in the flowing ammonia and was transformed into h–BN nanorods after subsequent crystallization. After crystallization at 1650°C for 2 h, the unique microstructure of h–BN nanorods was observed. 相似文献
20.
Olivier Renoult Jean-Pierre Boilot Frédéric Chaput Renée Papiernik Liliane G. Hubert-Pfalzgraf Martine Lejeune 《Journal of the American Ceramic Society》1992,75(12):3337-3340
The sol–gel method has been developed for the preparation of pure Ba(Mg1/3 Ta2/3 )O3 ceramics. This involves the reaction of the heterometallic alkoxide Ta2 Mg(OEt)12 with hydrated barium hydroxide Ba(OH)2 ·8H2 O. Complete crystallization of the sol–gel-derived powder is achieved at 600°C, leading to a cubic perovskite type phase. After sintering at 1400°C (2–5 h), a trigonal cell arises from Mg–Ta ordering (the degree of order is greater than 0.9), and about 98.5% of the theoretical density is obtained. Preliminary microwave dielectric measurements show that the dielectric constant and the unloaded Q u of the ceramics are 24.2 and 6750, respectively, at 7.7 GHz. 相似文献