Preparation of Ti2CuAl5 by Reactive Sintering

1988 ◽  
Vol 133 ◽  
Author(s):  
Arnulf J Maeland ◽  
Dave Narasimhan
Keyword(s):  
Intermetallic Compound ◽  
Intermetallic Compounds ◽  
Low Temperatures ◽  
Nickel Aluminides ◽  
Reactive Sintering ◽  
X Ray Diffraction ◽  
X Ray ◽  
New Process ◽  
Microhardness And Microstructure

ABSTRACTThe exothermic formation of intermetallic compounds from the constituent powders through reactive sintering at relatively low temperatures is a promising new process being explored for the preparation of nickel aluminides. The process is useful for synthesis of other intermetallics as well.We describe here the preparation of Ti2CuAl5 using the technique of reactive sintering. This intermetallic compound has a L12 structure which is also the structure of the very interesting Ni3Al intermetallic. Characterization of the Ti2CuAl5 phase is done by x-ray diffraction, microhardness, and microstructure.

The Synthesis of Ce-Filled CoSb3 and Characterization of its Magnetic and Structural Properties

2003 ◽  
Vol 793 ◽  
Author(s):  
Arwyn L. E. Smalley ◽  
Brandon Howe ◽  
David C. Johnson
Keyword(s):  
Low Temperatures ◽  
Magnetic Measurements ◽  
Rietveld Analysis ◽  
X Ray Diffraction ◽  
Electrical Measurements ◽  
X Ray ◽  
Ferromagnetic Component ◽  
Phase Pure ◽  
Powder Samples

ABSTRACTA series of cerium-containing CoSb3 samples were synthesized, with cerium quantities varying from 0 to 2 stoichiometric equivalents. These samples were annealed at low temperatures to crystallize the kinetically stable phases CexCo4Sb12 (x = 0–0.5). X-ray diffraction showed that these samples were phase pure, and Rietveld analysis on x-ray diffraction data from powder samples indicated that these samples were 25–88% crystalline. Electrical measurements showed that these samples are n-type, which was previously unknown in CexCo4Sb12. Magnetic measurements showed that the samples were paramagnetic due to the cerium being incorporated into the diamagnetic CoSb3 compound. In addition, they contained a ferromagnetic component that was attributed to the amorphous, cerium-containing phase.

In situ characterization of strain-induced crystallization of natural rubber by synchrotron radiation wide-angle X-ray diffraction: construction of a crystal network at low temperatures

Soft Matter ◽  
2019 ◽  
Vol 15 (4) ◽  
pp. 734-743 ◽  
Author(s):  
Pinzhang Chen ◽  
Jingyun Zhao ◽  
Yuanfei Lin ◽  
Jiarui Chang ◽  
Lingpu Meng ◽  
...  
Keyword(s):  
Low Temperatures ◽  
Structural Evolution ◽  
X Ray Diffraction ◽  
In Situ Characterization ◽  
X Ray ◽  
Crystal Network ◽  
Strain Induced Crystallization ◽  
Induced Crystallization

The structural evolution of NR during stretching at −40 °C and in the strain–temperature space.

Phase Transformation of Biphasic Granules of Gypsum and Carbonated Apatite at Low Temperatures

2016 ◽  
Vol 1133 ◽  
pp. 50-54 ◽  
Author(s):  
Siti Noorzidah Mohd Sabri ◽  
Syazana Abu Bakar ◽  
Abdul Yazid Abdul Manaf ◽  
Siti Farhana Hisham ◽  
Mohamad Azmirruddin Ahmad ◽  
...  
Keyword(s):  
Cross Section ◽  
Low Temperatures ◽  
Carbonate Content ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbonated Apatite ◽  
Infra Red ◽  
Different Temperatures ◽  
Bone Apatite

The purpose of this study was to prepare biphasic granules containing gypsum and carbonated apatite at low temperatures. The biphasic granules were prepared using dissolution-precipitation technique at three different temperatures 30°C, 40°C and 50°C. Characterization of the biphasic granules was determined by multiple analytical methods such as X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infra-red (FTIR), and CHN Analysis. The obtained granules were determined by XRD as biphasic granules containing bone apatite and gypsum. The cross-section of biphasic granules was observed by SEM. The formed bone apatite was identified as B-Type carbonated apatite using FTIR The carbonate content in biphasic granules fabricated at 30°C, 40°C and 50°C were recorded by CHN analysis as 5.0 wt%, 6.1 wt% and 6.25 wt%, respectively.

Low- and high-temperature structures of YbCuBi

2006 ◽  
Vol 221 (5-7) ◽  
Author(s):  
Andriy V. Tkachuk ◽  
Yurij Mozharivskyj ◽  
Arthur Mar
Keyword(s):  
Phase Transition ◽  
High Temperature ◽  
Intermetallic Compound ◽  
Single Crystal ◽  
Diffraction Study ◽  
Low Temperatures ◽  
Variable Temperature ◽  
X Ray Diffraction ◽  
X Ray

AbstractA variable temperature single-crystal X-ray diffraction study was undertaken on the intermetallic compound YbCuBi, which undergoes a phase transition at ∼375 K. At low temperatures (

CHARACTERIZATION OF Ni-RICH INTERMETALLIC COMPOUND Ni3Al FILMS WITH SLOW POSITRON BEAM

2009 ◽  
Vol 23 (26) ◽  
pp. 3097-3106 ◽  
Author(s):  
JIANDANG LIU ◽  
HUIMIN WENG ◽  
XIANGLEI CHEN ◽  
HUAIJIANG DU ◽  
BANGJIAO YE ◽  
...  
Keyword(s):  
Grain Size ◽  
Intermetallic Compound ◽  
Effective Diffusion ◽  
Positron Beam ◽  
Vacancy Cluster ◽  
X Ray Diffraction ◽  
Slow Positron ◽  
X Ray ◽  
S Parameter

Ni -rich intermetallic compound Ni 3 Al films were deposited using the dual-target magnetron co-sputtering method. The grain-boundary and grain-size characteristics of the as-deposited and post-annealed Ni 3 Al films were investigated using a slow positron beam. The results demonstrate a distinct change of S-parameter and positron effective diffusion length L eff values as samples were annealed at different ambient atmospheres and temperatures. It shows that the positron trapping center is mainly associated with intergranular vacancies, and changes to either the vacancy cluster size or the grain size have been invoked to explain the changes of the values of the S-parameter and L eff . Ni -rich oxygen- Ni 3 Al films were also studied. All films were identified using X-ray diffraction and the results confirm the conclusion obtained by the slow positron beam.

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.

High Resolution Replication of Organoclay Surfaces

1982 ◽  
Vol 40 ◽  
pp. 576-577
Author(s):  
W. W. Barker ◽  
W. E. Rigsby ◽  
V. J. Hurst ◽  
W. J. Humphreys
Keyword(s):  
Clay Mineral ◽  
Organic Molecule ◽  
Organic Molecules ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Naturally Occurring ◽  
Silicate Layers ◽  
Mineral Identification

Experimental clay mineral-organic molecule complexes long have been known and some of them have been extensively studied by X-ray diffraction methods. The organic molecules are adsorbed onto the surfaces of the clay minerals, or intercalated between the silicate layers. Natural organo-clays also are widely recognized but generally have not been well characterized. Widely used techniques for clay mineral identification involve treatment of the sample with H2 O2 or other oxidant to destroy any associated organics. This generally simplifies and intensifies the XRD pattern of the clay residue, but helps little with the characterization of the original organoclay. Adequate techniques for the direct observation of synthetic and naturally occurring organoclays are yet to be developed.

Synthesis and characterization of TiN / Ti / AISI 410 coatings

2018 ◽  
Vol 2 (1) ◽  
pp. 7
Author(s):  
S Chirino ◽  
Jaime Diaz ◽  
N Monteblanco ◽  
E Valderrama
Keyword(s):  
Synthesis And Characterization ◽  
Photoemission Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Columnar Grains ◽  
Tin Thin Films ◽  
Steel Aisi ◽  
Interacting Surfaces ◽  
Stainless Steel Aisi

The synthesis and characterization of Ti and TiN thin films of different thicknesses was carried out on a martensitic stainless steel AISI 410 substrate used for tool manufacturing. The mechanical parameters between the interacting surfaces such as thickness, adhesion and hardness were measured. By means of the scanning electron microscope (SEM) the superficial morphology of the Ti/TiN interface was observed, finding that the growth was of columnar grains and by means of EDAX the existence of titanium was verified.  Using X-ray diffraction (XRD) it was possible to observe the presence of residual stresses (~ -3.1 GPa) due to the different crystalline phases in the coating. Under X-ray photoemission spectroscopy (XPS) it was possible to observe the molecular chemical composition of the coating surface, being Ti-N, Ti-N-O and Ti-O the predominant ones.

Studies on the Preparation, Characterization and Solubility of -Cyclodextrin-Roxythromycin Inclusion Complexes

2009 ◽  
Vol 2 (2) ◽  
pp. 523-530
Author(s):  
D. Nagasamy Venkatesh ◽  
S. Karthick ◽  
M. Umesh ◽  
G. Vivek ◽  
R.M. Valliappan ◽  
...  
Keyword(s):  
Dissolution Rate ◽  
Inclusion Complexes ◽  
Phase Solubility ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ir Studies ◽  
Poorly Soluble ◽  
Poorly Soluble Drug

Roxythromycin/ β-cyclodextrin (Roxy/ β-CD) dispersions were prepared with a view to study the influence of β-CD on the solubility and dissolution rate of this poorly soluble drug. Phase-solubility profile indicated that the solubility of roxythromycin was significantly increased in the presence of β-cyclodextrin and was classified as AL-type, indicating the 1:1 stoichiometric inclusion complexes. Physical characterization of the prepared systems was carried out by differential scanning calorimetry (DSC), X-ray diffraction studies (XRD) and IR studies. Solid state characterization of the drug β-CD binary system using XRD, FTIR and DSC revealed distinct loss of drug crystallinity in the formulation, ostensibly accounting for enhancement of dissolution rate.

New Coordination Compounds of Fe(III) with Organic Ligands

2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Mihaela Flondor ◽  
Ioan Rosca ◽  
Doina Sibiescu ◽  
Mihaela-Aurelia Vizitiu ◽  
Daniel-Mircea Sutiman ◽  
...  
Keyword(s):  
Chemical Analysis ◽  
Complex Compounds ◽  
Organic Ligands ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Chemical Analysis ◽  
Structural Formulae ◽  
Paramagnetic Properties

In this paper the synthesis and the study of some complex compounds of Fe(III) with ligands derived from: 2-(4-chloro-phenylsulfanyl)-1-(2-hydroxy-3,5-diiodo-phenyl)-ethanone (HL1), 1-(3,5-dibromo-2-hydroxy-phenyl)-2-phenylsulfanyl-ethanone(HL2), and 2-(4-chloro-phenylsulfanyl)-1-(3,5-dibromo-2-hydroxy-phenyl)-ethanone (HL3) is presented. The characterization of these complexes is based on method as: the elemental chemical analysis, IR and ESR spectroscopy, M�ssbauer, the thermogravimetric analysis and X-ray diffraction. Study of the IR and chemical analysis has evidenced that the precipitates form are a complexes and the combination ratio of M:L is 1:2. The central atoms of Fe(III) presented paramagnetic properties and a octaedric hybridization. Starting from this precipitation reactions, a method for the gravimetric determination of Fe(III) with this organic ligands has been possible. Based on the experimental data on literature indications, the structural formulae of the complex compounds are assigned.

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