The Effect of Tungsten Nanoparticles on the Hardness of Sintered Sn-Cu-Co-W Alloys

2020 ◽  
Vol 992 ◽  
pp. 511-516
Author(s):  
Evgeniy Georgiyevich Sokolov ◽  
Alexander Vitalyevich Ozolin ◽  
Svetlana Alexandrovna Arefieva
Keyword(s):  
Tungsten Powder ◽  
Dispersion Hardening ◽  
X Ray Diffraction ◽  
X Ray ◽  
Centrifugal Mill ◽  
Size Of Particles ◽  
Tungsten Nanoparticles ◽  
Sintered Materials ◽  
Scanning Electron ◽  
Main Factor

The effect of tungsten nanoparticles and microparticles on the structure and hardness of sintered Sn–Cu–Co–W alloys has been studied. Tungsten powder of 19–24 μm sized particles was milled in a planetary-centrifugal mill, after which the size of particles was 25 nm to 20 μm. The milled and non-milled tungsten was then mixed with powders of tin, copper and cobalt. The specimens were compacted in moulds and sintered in vacuum at 820°C for 20 minutes. The structure of sintered materials was studied using X-ray diffraction analysis and scanning electron microscopy. Microhardness (HV0.01) of structural constituents and hardness of the materials were measured. It has been determined that it is alloys containing mechanically milled tungsten that have the highest hardness. The main factor influencing the rise of hardness is dispersion hardening with nanoparticles. A further factor is work hardening of tungsten microparticles during ball milling. The highest hardness of 109–111 HRB has been obtained in the Sn–Cu–Co–W alloy containing 23% wt. of milled tungsten, with the proportion of tin, copper and cobalt being 1/2.6/1.6.

The Effects of Al-Ca Compounds on Grain Refinement of Mg-Ca Alloys

2011 ◽  
Vol 686 ◽  
pp. 348-354 ◽  
Author(s):  
Shu Tao Xiong ◽  
Fu Sheng Pan ◽  
Bin Jiang ◽  
Xiao Ke Li
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Grain Size ◽  
Grain Refinement ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metallic Compound ◽  
Scanning Electron ◽  
Main Factor

In the present work, Al-Ca metallic compound was prepared in Mg-Ca alloys and the effects of Al-Ca metallic compound and different Al/Ca values on the grain refinement of Mg-Ca alloys were investigated by scanning electron microscopy and X-ray diffraction, and the mechanism of grain refinement of Mg-Ca alloys was discussed. The results showed that the grain size of Mg-0.5Ca alloy was obviously reduced from 550μm to 230μm due to the addition of Al. Al2Ca phase existed in these alloys and its morphology evolved from granular to rod-like. It is regarded as the main factor for the grain refinement.

Synthesis of Visible-Light Active Monoclinic WO3 by Thermal Oxidation of Tungsten Powder for Photoreduction of Cr(VI)

2020 ◽  
Vol 1010 ◽  
pp. 405-410
Author(s):  
Nurulhuda Bashirom ◽  
Qiao Ling Lee
Keyword(s):  
Visible Light ◽  
Thermal Oxidation ◽  
Oxygen Vacancies ◽  
Tungsten Powder ◽  
X Ray Diffraction ◽  
Oxide Interfaces ◽  
X Ray ◽  
Air Atmosphere ◽  
Visible Light Active ◽  
Scanning Electron

In this paper, visible-light-active monoclinic WO3 powders were synthesized by thermal oxidation of W powders at 200 – 1000 °C in air atmosphere. Morphology and crystal structure of annealed W powders were characterized by Scanning Electron Microscopy (SEM) and X-ray Diffraction (XRD), respectively. Based on SEM and XRD results, a spherical orthorhombic-W3O8 obtained at 200 °C was transformed into a dendritic monoclinic WO2 + tetragonal WO3 + monoclinic WO3 structures at 400 °C accompanied by a color transition from grey into green. At 600 °C, yellow monoclinic WO3 + monoclinic WO2.96 powder was produced that ascribed to oxygen vacancies. Photocatalytic activity of annealed W powders demonstrated 70.7% Cr (VI) removal after 150 min on sample annealed at 1000 °C. This ascribed to high photoactivity of monoclinic WO3. Nevertheless, the dendritic monoclinic WO2 + tetragonal WO3 + monoclinic WO3 obtained at 400 °C exhibited the lowest Cr (VI) photoreduction i.e. 45.2% implies less photoactive monoclinic WO2 and sluggish electron transport at oxide-oxide interfaces.

Dielectric Properties of CaCu3Ti4O12 Synthesized by Different Routes

2014 ◽  
Vol 975 ◽  
pp. 184-188 ◽  
Author(s):  
Tatiane Cristina Porfirio ◽  
Eliana Navarro Santos Muccillo
Keyword(s):  
Dielectric Properties ◽  
Sintering Temperature ◽  
Dielectric Losses ◽  
Electric Permittivity ◽  
X Ray Diffraction ◽  
Soft Chemistry ◽  
X Ray ◽  
Powder Characteristics ◽  
Sintered Materials ◽  
Scanning Electron

The perovskite CaCu3Ti4O12, with giant electric permittivity, was prepared by a soft chemistry route and by the solid state synthesis technique. The main purpose of this work is to verify the effects of the synthesis techniques on the powder characteristics, and the microstructure and dielectric properties of the sintered materials. The synthesized nanopowders were calcined, pressed into pellets and sintered using the same procedures as for the materials prepared by the conventional method. Phase analysis was performed by X-ray diffraction, microstructure observations were carried out by scanning electron microscopy, and the dielectric properties were studied by impedance spectroscopy. The electric permittivity ranged from 11,600 to 27,000 and from 5,000 to 9,000 for specimens prepared by the conventional and the soft chemistry techniques, respectively, and the dielectric losses varied between 0.1 and 1.3 (conventional) and 0.095 and 0.3 (soft chemistry) depending on the sintering temperature.

Preparation and Characterization of Bi4Si3O12 Powders by Templates-Hydrothermal Method

2011 ◽  
Vol 239-242 ◽  
pp. 2149-2152
Author(s):  
Qing Ju Ning ◽  
Bang Qing Wang ◽  
Su Hang Gu ◽  
Fang Fang Guo
Keyword(s):  
Electron Microscopy ◽  
Salt Content ◽  
Morphological Characteristics ◽  
Molten Salt Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size Of Particles ◽  
Transmission Scanning Electron Microscopy ◽  
Scanning Electron

Bi4Si3O12powders are prepared by template -hydrothermal used Bi4Si3O12as a template made by molten-salt method. The phase composition and morphological characteristics of BSO nanoparticles were analyzed and observed by X-ray diffraction and transmission scanning electron microscopy. The results show that with the salt content of 50wt%, calcination temperature 770°C, it can form a high purity Bi4Si3O12template. A single Bi4Si3O12phase can be obtained by template –hydrothermal, with template addition 30wt%, the reaction temperature 240°C, holding time for 24h, and prolonging the reaction time is conducive to Bi4Si3O12grain growth. The powders have a good dispersion, and size of particles is about 10μm or so, and show a columnar shape.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

Identification of calcium oxalate crystals in dried or fixed tobacco leaf

1984 ◽  
Vol 42 ◽  
pp. 288-289
Author(s):  
Vicki L. Baliga ◽  
Mary Ellen Counts
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Calcium Oxalate ◽  
Growth And Development ◽  
Polarized Light ◽  
Calcium Oxalate Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.

Sem and X-Ray Analysis of Renal and Biliary Calculi

1976 ◽  
Vol 34 ◽  
pp. 306-307
Author(s):  
R. J. Narconis ◽  
G. L. Johnson
Keyword(s):  
Chemical Constituents ◽  
Natural State ◽  
X Ray Diffraction ◽  
Chemical Methods ◽  
X Ray ◽  
Additional Dimension ◽  
Biliary Calculi ◽  
Calculus Formation ◽  
Scanning Electron

Analysis of the constituents of renal and biliary calculi may be of help in the management of patients with calculous disease. Several methods of analysis are available for identifying these constituents. Most common are chemical methods, optical crystallography, x-ray diffraction, and infrared spectroscopy. The application of a SEM with x-ray analysis capabilities should be considered as an additional alternative.A scanning electron microscope equipped with an x-ray “mapping” attachment offers an additional dimension in its ability to locate elemental constituents geographically, and thus, provide a clue in determination of possible metabolic etiology in calculus formation. The ability of this method to give an undisturbed view of adjacent layers of elements in their natural state is of advantage in determining the sequence of formation of subsequent layers of chemical constituents.

Environmental scanning electron microscopy of fresh human gallstones reveals new morphologies of precipitated calcium salts

1992 ◽  
Vol 50 (2) ◽  
pp. 1322-1323
Author(s):  
Howard S. Kaufman ◽  
Keith D. Lillemoe ◽  
John T. Mastovich ◽  
Henry A. Pitt
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
X Ray Diffraction ◽  
Calcium Salts ◽  
Cholesterol Gallstones ◽  
X Ray ◽  
Ca Carbonate ◽  
Scanning Electron

Gallstones contain precipitated cholesterol, calcium salts, and proteins. Calcium (Ca) bilirubinate, palmitate, phosphate, and carbonate occurring in gallstones have variable morphologies but characteristic windowless energy dispersive x-ray (EDX) spectra. Previous studies of gallstone microstructure and composition using scanning electron microscopy (SEM) with EDX have been limited to dehydrated samples. In this state, Ca bilirubinates appear as either glassy masses, which predominate in black pigment stones, or as clusters, which are found mostly in cholesterol gallstones. The three polymorphs of Ca carbonate, calcite, vaterite, and aragonite, have been identified in gallstones by x-ray diffraction, however; the morphologies of these crystals vary in the literature. The purpose of this experiment was to study fresh gallstones by environmental SEM (ESEM) to determine if dehydration affects gallstone Ca salt morphology.Gallstones and bile were obtained fresh at cholecystectomy from 6 patients. To prevent dehydration, stones were stored in bile at 37°C. All samples were studied within 4 days of procurement.

Photocatalytic activity of TiO2 synthesized by anodization and anodic spark deposition

MRS Advances ◽  
2020 ◽  
Vol 5 (61) ◽  
pp. 3141-3152
Author(s):  
Alma C. Chávez-Mejía ◽  
Génesis Villegas-Suárez ◽  
Paloma I. Zaragoza-Sánchez ◽  
Rafael Magaña-López ◽  
Julio C. Morales-Mejía ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Surface Characteristics ◽  
Amorphous Solids ◽  
X Ray Diffraction ◽  
X Ray ◽  
Catalytic Activities ◽  
Anodic Spark Oxidation ◽  
Porous Surfaces ◽  
Scanning Electron

AbstractSeveral photocatalysts, based on titanium dioxide, were synthesized by spark anodization techniques and anodic spark oxidation. Photocatalytic activity was determined by methylene blue oxidation and the catalytic activities of the catalysts were evaluated after 70 hours of reaction. Scanning Electron Microscopy and X Ray Diffraction analysis were used to characterize the catalysts. The photocatalyst prepared with a solution of sulfuric acid and 100 V presented the best performance in terms of oxidation of the dye (62%). The electric potential during the synthesis (10 V, low potential; 100 V, high potential) affected the surface characteristics: under low potential, catalyst presented smooth and homogeneous surfaces with spots (high TiO2 concentration) of amorphous solids; under low potential, catalyst presented porous surfaces with crystalline solids homogeneously distributed.

The Effect of the Microstructure of Diffusion Barriers on the Palladium Activation for Electroless Copper Deposition

2002 ◽  
Vol 716 ◽  
Author(s):  
Seok Woo Hong ◽  
Yong Sun Lee ◽  
Ki-Chul Park ◽  
Jong-Wan Park
Keyword(s):  
Electron Microscopy ◽  
Diffusion Barriers ◽  
Copper Deposition ◽  
X Ray Diffraction ◽  
Plan View ◽  
X Ray ◽  
Transmission Electron ◽  
Electroless Copper ◽  
Sheet Resistance Measurement ◽  
Scanning Electron

AbstractThe effect of microstructure of dc magnetron sputtered TiN and TaN diffusion barriers on the palladium activation for autocatalytic electroless copper deposition has been investigated by using X-ray diffraction, sheet resistance measurement, field emission scanning electron microscopy (FE-SEM) and plan view transmission electron microscopy (TEM). The density of palladium nuclei on TaN diffusion barrier increases as the grain size of TaN films decreases, which was caused by increasing nitrogen content in TaN films. Plan view TEM results of TiN and TaN diffusiton barriers showed that palladium nuclei formed mainly on the grain boundaries of the diffusion barriers.

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