scholarly journals Solid-state reaction in nanoparticulate alumina/LZSA glass-ceramic composites

Cerâmica ◽  
2018 ◽  
Vol 64 (371) ◽  
pp. 397-402
Author(s):  
O. R. K. Montedo ◽  
F. Raupp-Pereira ◽  
A. P. N. de Oliveira
Keyword(s):  
Solid State ◽  
Glass Ceramic ◽  
Coefficient Of Thermal Expansion ◽  
Raw Materials ◽  
Glass Frit ◽  
Ceramic Composites ◽  
Solid State Reactions ◽  
X Ray Diffraction ◽  
Dry Powders ◽  
Xrd Study

Abstract In this work, some properties, such as sinterability, modulus of elasticity (E), coefficient of thermal expansion (CTE) and dielectric constant (εr), of composites constituted by nanoparticulate alumina (27-43 nm, 35 m2.g-1) in different contents (0 to 77 vol%) and a LZSA glass-ceramic composition (17.7Li2O-5.2ZrO2-68.1SiO2-9.0Al2O3, molar basis) were evaluated. Dry powders of the raw materials (alumina and LZSA parent glass, frit) were uniaxially pressed (40 MPa) and the obtained compacts were sintered at 600-950 °C (1 h holding time). X-ray diffraction (XRD) study was performed in order to investigate the solid-state reactions occurred in LZSA-based compositions during sintering. XRD results were correlated to the CTE, E and εr of sintered samples. The CTE of the obtained composites decreased as alumina content increased mainly due to the β-spodumeness (solid solution Li2O.Al2O3.4-10SiO2) formation. The results concerning the E (22.3±1.5 GPa) and εr (3.1±1.3) for the composite with 5.6 vol% addition sintered at 850 °C for 1 h indicated, in a preliminary way, the possibility of development of materials with suitable properties for applications concerning to the low temperature co-fired ceramic (LTCC) technology.

TEM studies of solid-state reactions in sputter-deposited Nb/Al multilayer thin films

1996 ◽  
Vol 54 ◽  
pp. 1020-1021
Author(s):  
F. Ma ◽  
S. Vivekanand ◽  
K. Barmak ◽  
C. Michaelsen
Keyword(s):  
Thin Films ◽  
Solid State ◽  
Stoichiometric Composition ◽  
Analytical Electron Microscopy ◽  
Grain Structure ◽  
Solid State Reactions ◽  
Multilayer Thin Films ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sputter Deposited

Solid state reactions in sputter-deposited Nb/Al multilayer thin films have been studied by transmission and analytical electron microscopy (TEM/AEM), differential scanning calorimetry (DSC) and X-ray diffraction (XRD). The Nb/Al multilayer thin films for TEM studies were sputter-deposited on (1102)sapphire substrates. The periodicity of the films is in the range 10-500 nm. The overall composition of the films are 1/3, 2/1, and 3/1 Nb/Al, corresponding to the stoichiometric composition of the three intermetallic phases in this system.Figure 1 is a TEM micrograph of an as-deposited film with periodicity A = dA1 + dNb = 72 nm, where d's are layer thicknesses. The polycrystalline nature of the Al and Nb layers with their columnar grain structure is evident in the figure. Both Nb and Al layers exhibit crystallographic texture, with the electron diffraction pattern for this film showing stronger diffraction spots in the direction normal to the multilayer. The X-ray diffraction patterns of all films are dominated by the Al(l 11) and Nb(l 10) peaks and show a merging of these two peaks with decreasing periodicity.

Facile Solid State Method Route Synthesis and Enhance Visible Light Activities of BiVO4 by Doping Co

2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu
Keyword(s):  
Solid State ◽  
Visible Light ◽  
Catalytic Effect ◽  
Catalytic Properties ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Solid State Method ◽  
Illumination Time ◽  
X Ray ◽  
State Method

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.

Preparation and Photocatalytic Activity of Cu/BiVO4 by Solid State Grinding Method for Degradation of Methyl Orange

2016 ◽  
Vol 703 ◽  
pp. 321-325
Author(s):  
Hai Feng Chen ◽  
Jia Mei Chen ◽  
Zhi Xue Pan
Keyword(s):  
Methyl Orange ◽  
Solid State ◽  
Visible Light ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Illumination Time ◽  
Grinding Method ◽  
Ft Ir ◽  
Degradation Of Methyl Orange

In this work, novel Cu/BiVO4 photocatalyst were prepared by a low-temperature solid state grinding method using Bi (NO3)3•5H2O, NH4VO3 and Cu (NO3)2•2H2O as raw materials. The structure and properties of the samples were characterized by Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD) and UV-vis diffused reflectance spectroscopy (DRS); Using the degradation of methyl orange (MO) as the probe, it was simulated as the degradation of sewage under the visible light to study the influence of the illumination time and the amount of photocatalysts. Compared with the pure BiVO4, the visible-light absorption scope of BiVO4 was broadened by doping Cu, the UV-Visible absorption edges were slightly red shift and the band gap was narrower. Comparatively speaking, the results indicted that the doped Cu enhanced the photocatalytic activities of BiVO4.

Microstructure and Properties of Calcium Borosilicate and Borosilicate Glass-Ceramic Composites

2008 ◽  
Vol 368-372 ◽  
pp. 1422-1425 ◽  
Author(s):  
An Guo Lu ◽  
Tai Qiu
Keyword(s):  
Borosilicate Glass ◽  
Glass Ceramic ◽  
Mass Fraction ◽  
Sintering Temperature ◽  
Coefficient Of Thermal Expansion ◽  
Ceramic Composites ◽  
Glass Content ◽  
Microstructure And Properties ◽  
Calcium Borosilicate ◽  
Crystal Phases

Calcium borosilicate (CaO-B2O3-SiO2, CBS) glass based glass-ceramic composites were prepared by introducing borosilicate glass. The effects of borosilicate glass and firing temperature on the microstructure and properties of the glass-ceramic composites were investigated. The results showed that the composites containing 0~40% (in mass fraction, the same below) borosilicate glass can be sintered at 850°C. The dielectric constant (εr) decreases with the increase of borosilicate glass content and can be adjusted in the range of 5.6~6.6. The coefficient of thermal expansion (CTE) increases with the increase of borosilicate glass content. Increasing sintering temperature favors the precipitations of crystal phases, which have lower εr than CBS glass, resulting in the decrease of εr for the composites.

Devitrification in SiO2-B2O3-Al2O3-La2O3-TiO2 Glass during the Infiltration of Ceramic Composite

2016 ◽  
Vol 881 ◽  
pp. 77-82
Author(s):  
Afonso Chimanski ◽  
Amanda Martins Jordão ◽  
Paulo Francisco Cesar ◽  
Humberto Naoyuki Yoshimura
Keyword(s):  
Ceramic Composite ◽  
Raw Materials ◽  
Porous Alumina ◽  
Ceramic Composites ◽  
X Ray Diffraction ◽  
Infiltration Process ◽  
X Ray ◽  
Dental Prostheses ◽  
Devitrification Process ◽  
Natural Teeth

Dental prostheses made of ceramic composites infiltrated with glasses have been used due to their biocompatibility and possibility to mimic the natural teeth. In this study, the devitrification behavior of 20SiO2-25B2O3-25Al2O3-15La2O3-15TiO2 glass during the infiltration process in a porous alumina preform was investigated. Glass frits were prepared by melting the raw materials at 1500 °C for 60 min. The glass was infiltrated into the alumina preform at 1,150 or 1,200 °C for 60 min. The specimens were characterized by X-ray diffraction analysis and scanning electron microscopy. After the infiltration, it was possible to note that the devitrification process occurred in the remaining glass (excess glass that did not infiltrate in the preform), forming mostly aluminum borate and mullite crystalline phases. However, within the infiltrated composite no devitrification was noticed in the infiltrated glass. Possible explanations for this behavior are discussed.

A Novel Wear Resistant Glass-Ceramic Coating Material

2011 ◽  
Vol 686 ◽  
pp. 521-527
Author(s):  
Ye Han ◽  
Shu Yu Yao ◽  
Wei Wei Zhang ◽  
Ming Gu ◽  
Yu Sui Yao
Keyword(s):  
Glass Ceramic ◽  
Ceramic Coating ◽  
Coefficient Of Thermal Expansion ◽  
Xrd Analysis ◽  
Coating Material ◽  
X Ray Diffraction ◽  
Coating Materials ◽  
Wear Resistant ◽  
X Ray ◽  
Glass Ceramic Coating

A novel wear resistant glass-ceramic coating system (based on SiO2-B2O3-Al2O3 glass system) on iron based substrate was developed. Friction coefficient, wear rate and coefficient of thermal expansion of coating material were evaluated using suitable methods. The coating materials and the resultant coatings were characterized using differential thermal analysis (DTA), X-ray diffraction analysis (XRD) and Scanning Electron Microscope (SEM). XRD analysis of the coating materials showed presence of a number of microcrystal. SEM micrographs indicate strong chemical bonding at the iron-ceramic interface. The coating material showed perfect properties for protection the iron substrate from abrasion.

Solid-state reaction of Pt thin film with single-crystal (001) β–SiC

1994 ◽  
Vol 9 (3) ◽  
pp. 648-657 ◽  
Author(s):  
J.S. Chen ◽  
E. Kolawa ◽  
M-A. Nicolet ◽  
R.P. Ruiz ◽  
L. Baud ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Solid State ◽  
Single Crystal ◽  
Atomic Scale ◽  
Solid State Reactions ◽  
Main Reaction ◽  
Main Reaction Product ◽  
X Ray Diffraction ◽  
X Ray ◽  
Amorphous Interlayer

Thermally induced solid-state reactions between a 70 nm Pt film and a single-crystal (001) β-SiC substrate at temperatures from 300 °C to 1000 °C for various time durations are investigated by 2 MeV He backscattering spectrometry, x-ray diffraction, secondary ion mass spectrometry, scanning electron microscopy, and cross-sectional transmission electron microscopy. Backscattering spectrometry shows that Pt reacts with SiC at 500 °C. The product phase identified by x-ray diffraction is Pt3Si. At 600–900 °C, the main reaction product is Pt2Si, but the depth distribution of the Pt atoms changes with annealing temperature. When the sample is annealed at 1000 °C, the surface morphology deteriorates with the formation of some dendrite-like hillocks; both Pt2Si and PtSi are detected by x-ray diffraction. Samples annealed at 500–900 °C have a double-layer structure with a silicide surface layer and a carbon-silicide mixed layer below in contact with the substrate. The SiC—Pt interaction is resolved at an atomic scale with high-resolution electron microscopy. It is found that the grains of the sputtered Pt film first align themselves preferentially along an orientation of {111}Pt//{001}SiC without reaction between Pt and SiC. A thin amorphous interlayer then forms at 400 °C. At 450 °C, a new crystalline phase nucleates discretely at the Pt-interlayer interface and projects into or across the amorphous interlayer toward the SiC, while the undisturbed amorphous interlayer between the newly formed crystallites maintains its thickness. These nuclei grow extensively down into the substrate region at 500 °C, and the rest of the Pt film is converted to Pt3Si. Comparison between the thermal reaction of SiC-Pt and that of Si–Pt is discussed.

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