The Synthesis of Ultrafine Ba/Sr Titanate Powders

1991 ◽  
Vol 249 ◽  
Author(s):  
C.H. Lin ◽  
T.S. Yan ◽  
T.S. Chin
Keyword(s):  
Aqueous Solution ◽  
Particle Size ◽  
Solid State ◽  
Solid Solutions ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
Tem Analysis ◽  
X Ray ◽  
Solid State Sintering ◽  
Sintering Method

ABSTRACTBa/Sr titanate powders were obtained by reacting TiO2.xH2O gel in Ba(OH)2 and/or Sr(OH)2 aqueous solution. Different reaction temperatures between 68°C and 98°C and different mole ratios of Ba(OH)2 and Sr(OH)2 were used.X-ray diffraction analysis showed that the titanate powders are cubic, and they are solid solutions of barium and strontium. The lattace spaces of the titanates are affected by the Ba(OH)g/ Sr(OH)g, mole ratio. TEM analysis showed that the titanate powders were spherical, ultrafine, and almost monodispersed. The particle size of the powders is about from 41 to 50 nm depending on the reaction temperature.The titanate powders were compacted and sintered at various temperatures. The best sintering temperature of the powders is about 150°C lower than that of powders made by solid state sintering method.

PHASE STRUCTURE, PIEZOELECTRIC AND MULTIFERRIOC BEHAVIOR OF (K0.48Na0.52)NbO3-Co2O3 PIEZOELECTRIC CERAMICS

2011 ◽  
Vol 04 (03) ◽  
pp. 225-229 ◽  
Author(s):  
WENJUAN WU ◽  
DINGQUAN XIAO ◽  
JIAGANG WU ◽  
JING LI ◽  
JIANGUO ZHU
Keyword(s):  
Room Temperature ◽  
Sintering Temperature ◽  
Magnetic Behavior ◽  
Orthorhombic Phase ◽  
Piezoelectric Ceramics ◽  
X Ray Diffraction ◽  
Two Phase ◽  
X Ray ◽  
Solid State Sintering ◽  
Sintering Method

( K 0.48 Na 0.52) NbO 3-x% Co 2 O 3 (x = 0, 0.03 and 0.05) (KNN-x% Co2O3 ) lead-free piezoelectric ceramics were prepared by the conventional solid-state sintering method. An orthorhombic phase was observed for all KNN-x% Co2O3 ceramics at room temperature, and two phase transitions were confirmed by the high temperature X-ray diffraction and the temperature dependence of the dielectric constant. The Co2O3 greatly improves the density and decreases the sintering temperature of KNN ceramics. The KNN-0.05 mol%Co2O3 ceramic exhibits good properties (d33 = 120 pC/N , k p = 0.41, Q m = 213 and T c = 407°C) and a good age stability. The multiferroic behavior was also observed at room temperature for the KNN-0.05 mol%Co2O3 ceramic, as confirmed by P–E loops and magnetic behavior.

scholarly journals Structure and some magnetic properties of (BiFeO3)x-(BaTiO3)1−x solid solutions prepared by solid-state sintering

Nukleonika ◽  
2015 ◽  
Vol 60 (1) ◽  
pp. 81-85 ◽  
Author(s):  
Karol Kowal ◽  
Maciej Kowalczyk ◽  
Dionizy Czekaj ◽  
Elżbieta Jartych
Keyword(s):  
Magnetic Properties ◽  
Solid State ◽  
Solid Solutions ◽  
Hyperfine Magnetic Field ◽  
X Ray Diffraction ◽  
Soaking Time ◽  
Cubic Symmetry ◽  
Solid State Sintering ◽  
Perovskite Type ◽  
Sintering Method

Abstract This paper presents the results of the study on structure and magnetic properties of the perovskite-type (BiFeO3)x-(BaTiO3)1−x solid solutions. The samples differing in the chemical composition (x = 0.9, 0.8, and 0.7) were produced according to the conventional solid-state sintering method from the mixture of powders. Moreover, three different variants of the fabrication process differing in the temperatures and soaking time were applied. The results of X-ray diffraction (XRD), Mössbauer spectroscopy (MS), and vibrating sample magnetometry (VSM) were collected and compared for the set of the investigated materials. The structural transformation from rhombohedral to cubic symmetry was observed for the samples with x = 0.7. With increasing of BaTiO3 concentration Mössbauer spectra become broadened reflecting various configurations of atoms around 57Fe probes. Moreover, gradual decreasing of the average hyperfine magnetic field and macroscopic magnetization were observed with x decreasing.

scholarly journals Interaction between WC and Inconel 625 under Solid and Liquid State Sintering Conditions

Metals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 666
Author(s):  
Lorena Emanuelli ◽  
Alberto Molinari ◽  
Massimo Pellizzari
Keyword(s):  
Solid Solutions ◽  
Sintering Temperature ◽  
Inconel 625 ◽  
High Temperature Strength ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hard Metals ◽  
Solid State Sintering ◽  
Sintering Conditions

Cobalt is the most used metal binder in hard metals since its extraordinary wetting, adhesion and mechanical properties. Nevertheless, it has been recognized genotoxic and cancerogenic with higher toxicity in combination with WC. To substitute Co with an alternative binder, the interaction between the binder and WC must be taken into account. In this work, IN625 is considered as a binder alternative due to its desirable combination of high-temperature strength and corrosion/oxidation resistance. A characterization of the interaction between WC and IN625 was carried out by means of Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDXS) and X-Ray Diffraction (XRD). Depending on the sintering temperatures, different phases were evidenced at the WC–IN625 superalloy interface. From 1250 °C to 1300 °C, where solid-state sintering takes place, (Cr,Mo)23C6, W2C and (Cr,W) solid solutions were detected. At a sintering temperature of 1350 °C, IN625 melts and the formation of additional phases, such as an intermetallic Ni4W phase and (Mo,W) and (Mo,Nb) solid solutions, were observed. The precipitation of NbC and (Mo,Cr)23C6 carbides in IN625 was also detected.

scholarly journals Synthesis and Na+ Ion Conductivity of Stoichiometric Na3Zr2Si2PO12 by Liquid-Phase Sintering with NaPO3 Glass

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3790
Author(s):  
Yongzheng Ji ◽  
Tsuyoshi Honma ◽  
Takayuki Komatsu
Keyword(s):  
Solid State ◽  
Liquid Phase ◽  
Sintering Temperature ◽  
Liquid Phase Sintering ◽  
Ion Conductivity ◽  
X Ray Diffraction ◽  
Conventional Solid State Reaction ◽  
X Ray ◽  
Sintering Time ◽  
Lower Activation

Sodium super ionic conductor (NASICON)-type Na3Zr2Si2PO12 (NZSP) with the advantages of the high ionic conductivity, stability and safety is one of the most famous solid-state electrolytes. NZSP, however, requires the high sintering temperature about 1200 °C and long sintering time in the conventional solid-state reaction (SSR) method. In this study, the liquid-phase sintering (LPS) method was applied to synthesize NZSP with the use of NaPO3 glass with a low glass transition temperature of 292 °C. The formation of NZSP was confirmed by X-ray diffraction analyses in the samples obtained by the LPS method for the mixture of Na2ZrSi2O7, ZrO2, and NaPO3 glass. The sample sintered at 1000 °C for 10 h exhibited a higher Na+ ion conductivity of 1.81 mS/cm at 100 °C and a lower activation energy of 0.18 eV compared with the samples prepared by the SSR method. It is proposed that a new LPE method is effective for the synthesis of NZSP and the NaPO3 glass has a great contribution to the Na+ diffusion at the grain boundaries.

Preparation and Microstructure of Pressureless Sintered Si2ON2-SiC Ceramic

2011 ◽  
Vol 335-336 ◽  
pp. 699-703
Author(s):  
Hui Hui Tan ◽  
Zhu Xing Tang ◽  
Xia Zhao ◽  
He Zhang
Keyword(s):  
Bulk Density ◽  
Sintering Temperature ◽  
Pressureless Sintering ◽  
Nitriding Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Effect Of Additives ◽  
Sic Ceramic ◽  
Sintering Method ◽  
Scanning Electron

This paper introduces Si2ON2-SiC ceramic fabricated by pressureless sintering method and studies the effect of additives, nitriding temperatures on bulk density, porosity, phase composition and microstructure. It is discovered that additives MgO, CeO2 can increase the densities of Si2ON2-SiC ceramic apparently, and MgO additive has a better effect than CeO2. Nitriding temperature also is an important factor. The bulk density of the specimen with MgO additive reaches maximum at 1.91 g/cm3 when sintered at 1450 °C, and the bulk density of specimen with CeO2 additive is 1.86 g/cm3 at the same condition while the bulk density of the specimen without additive is only 1.75 g/cSuperscript textm3. The X-ray diffraction and scanning electron microscopy of the specimens show that the amount of Si2ON2 increase with the sintering temperature increase. But when the temperature is higher than 1500 °C the Si2ON2 grains will decompose into Si3N4, and Si2ON2 will vanish at 1550 °C

scholarly journals Effect of Sintering Temperature on Property of Low-Density Ceramic Proppant Adding Coal Gangue

2019 ◽  
Vol 26 (1) ◽  
pp. 94-98
Author(s):  
Jianying HAO ◽  
Huilan HAO ◽  
Yunfeng GAO ◽  
Xianjun LI ◽  
Mei QIN ◽  
...  
Keyword(s):  
Solid Waste ◽  
Bulk Density ◽  
Apparent Density ◽  
Sintering Temperature ◽  
Coal Gangue ◽  
Low Density ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sintering Method ◽  
Waste Coal

Calcined flint clay (45.6 wt.% Al2O3) and solid waste coal gangue were used to prepare low-density ceramic proppant by solid state sintering method. The density and breakage ratio of the ceramic proppant were systematically investigated as a function of sintering temperature. The morphology and phase composition of the ceramic proppant were examined by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The results show that the ceramic proppant is composed of rod-like mullite and granular cristobalite. Bulk density and apparent density of the proppant first rise and then slightly decrease with increasing the sintering temperature, while breakage ratios under 35 MPa and 52 MPa pressure gradually decrease and then increase. As the sintering temperature increases up to 1400 °C, the ceramic proppant shows denser microstructure. The proppant sintered at 1400 °C have the best performance with 1.27 g/cm3 of bulk density, 2.79 g/cm3 of apparent density, 3.27 % of breakage ratio under 35 MPa closed pressure and 8.36 % of breakage ratio under 52 MPa closed pressure, which conform to the requirement of low-density ceramic proppant. The addition of solid waste can greatly reduce the preparation cost of the ceramic proppant.

Effect of Process on the Dielectric Properties of BaTiO3-Based X9R Ceramics

2014 ◽  
Vol 906 ◽  
pp. 18-24 ◽  
Author(s):  
Bao Lin Zhang ◽  
Bin Bin Zhang ◽  
Ning Ning Wang ◽  
Jing Ming Fei
Keyword(s):  
Particle Size ◽  
Dielectric Properties ◽  
Milling Time ◽  
Sintering Temperature ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Sintered Ceramic ◽  
X Ray ◽  
Particle Size Analyzer

The effect of milling time and sintering process on the dielectric properties of BaTiO3-based X9R ceramics was investigated. The characterization of the raw powders and the sintered ceramic was carried out by X-ray diffraction and scanning electron microscopy. The particle size distribution of the mixed powders was examined by Laser Particle Size Analyzer. The results shown that with the milling time extended, the Cruie Peak was depressed, or even disappeared. Moreover, with the rise of sintering temperature, the dielectric constant of the ceramics increased and the dielectric loss decreased gradually. Eventually, by milling for 11h and sintering at 1090°Cfor 2h, good dielectric properties were obtained, which were ε25°C≥ 2526, εr/εr25°C≤± 12% (–55~200°C), tanδ≤1.12% (25°C).

Two new CdII MOFs of 1,4-bis(1H-benzimidazol-1-yl)butane and flexible dicarboxylate ligands: luminescence sensing towards Fe3+

2020 ◽  
Vol 76 (11) ◽  
pp. 1024-1033
Author(s):  
Fang-Hua Zhao ◽  
Shi-Yao Li ◽  
Wen-Yu Guo ◽  
Zi-Hao Zhao ◽  
Xiao-Wen Guo ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Solid State ◽  
Hydrogen Bonds ◽  
Layer Structure ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vis Spectroscopy

Two new CdII MOFs, namely, two-dimensional (2D) poly[[[μ2-1,4-bis(1H-benzimidazol-1-yl)butane](μ2-heptanedioato)cadmium(II)] tetrahydrate], {[Cd(C7H10O4)(C18H18N4)]·4H2O} n or {[Cd(Pim)(bbimb)]·4H2O} n (1), and 2D poly[diaqua[μ2-1,4-bis(1H-benzimidazol-1-yl)butane](μ4-decanedioato)(μ2-decanedioato)dicadmium(II)], [Cd2(C10H16O4)2(C18H18N4)(H2O)2] n or [Cd(Seb)(bbimb)0.5(H2O)] n (2), have been synthesized hydrothermally based on the 1,4-bis(1H-benzimidazol-1-yl)butane (bbimb) and pimelate (Pim2−, heptanedioate) or sebacate (Seb2−, decanedioate) ligands. Both MOFs were structurally characterized by single-crystal X-ray diffraction. In 1, the CdII centres are connected by bbimb and Pim2− ligands to generate a 2D sql layer structure with an octameric (H2O)8 water cluster. The 2D layers are further connected by O—H...O hydrogen bonds, resulting in a three-dimensional (3D) supramolecular structure. In 2, the CdII centres are coordinated by Seb2− ligands to form binuclear Cd2 units which are linked by bbimb and Seb2− ligands into a 2D hxl layer. The 2D layers are further connected by O—H...O hydrogen bonds, leading to an 8-connected 3D hex supramolecular network. IR and UV–Vis spectroscopy, thermogravimetric analysis and solid-state photoluminescence analysis were carried out on both MOFs. Luminescence sensing experiments reveal that both MOFs have good selective sensing towards Fe3+ in aqueous solution.

Synthesis, Transport And Microstructural Properties of Nd1.85Ce0.15CuO4‐δ

1989 ◽  
Vol 169 ◽  
Author(s):  
Jong‐Gyu Lee ◽  
K.V. Ramanujachary ◽  
M. Greenblattî
Keyword(s):  
Solid State ◽  
Solution Method ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
Solid State Route ◽  
Solution Precursor ◽  
Solution Route ◽  
State Resistance

AbstractThe n‐type superconductor, Nd1.85Ce0.15CuO4‐δ has been prepared by solid state reaction and solution precursor techniques under various conditions and characterized by means of X‐ray diffraction, magnetic susceptibility, electrical resistivity and SEM measurements. Samples prepared by solution method displayed higher normal state resistance but better superconducting volume fractions than those prepared by conventional ceramic techniques. In addition, the solution precursor technique reduces the sintering temperature from 1150°C (used for solid‐state route) to 1000°C in achieving the superconducting phase. The solution‐route yields particles with relatively uniform size distribution, but poor connectivity between the grains. In contrast, the solid state preparations yield well connected grains but with a larger distribution of sizes. The observed differences in the superconducting properties of samples prepared by different techniques have been attributed to the differences in their microstructure.

Preparation and Properties of CaF2 Nano-Powder

2016 ◽  
Vol 680 ◽  
pp. 257-260
Author(s):  
Meng Yun Dong ◽  
Cheng Zhang ◽  
Jin Feng Xia ◽  
Hong Qiang Nian ◽  
Dan Yu Jiang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Particle Size ◽  
Sintering Temperature ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nano Powder ◽  
Direct Precipitation ◽  
Scanning Electron

CaF2 nano-power was prepared by direct precipitation methods with Ca(NO3)2 and KF as raw materials. The influences of presintering temperature and sintering temperature on the particle size and distribution of CaF2 nano-power were studied by X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM). This study provided an experimental method for preparation of CaF2 nano-power. The results show that the best presintering temperature of CaF2 nano-power is 500°C and the best sintering temperature of CaF2 ceramic is 900°C.

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