Mechanical Synthesis and Heat Treatment of Ni75Ti25 Alloy

2013 ◽  
Vol 203-204 ◽  
pp. 390-393 ◽  
Author(s):  
Joanna Panek ◽  
Bożena Bierska-Piech ◽  
Jolanta Niedbała
Keyword(s):  
Annealing Treatment ◽  
Milling Process ◽  
X Ray Diffraction ◽  
Mechanical Synthesis ◽  
Powder Morphology ◽  
X Ray ◽  
Lattice Strains ◽  
Crystallite Sizes ◽  
Titanium Powders ◽  
Xrd Method

The investigations of the microstructure changes of Ni75Ti25powder prepared by mechanical alloying in as-milled state and after annealing treatment were performed. The X-ray diffraction (XRD) method was used to investigate a mechanically induced solid state reaction between nickel and titanium powders. The crystallite sizes and lattice strains were analyzed by using Williamson-Hall method. The compacted powder morphology was analyzed by SEM method. The Ni(Ti) solid solution was formed as a result of the milling process. The crystallite sizes of all alloys are below 100 nm. The annealing treatment, in the temperature range of 773 K to 1173 K leads to reduction of the breadth of Ni(Ti) diffraction lines, which indicates at the increase in size of crystallites. However, the phase composition of annealed Ti75Ni25powder does not change, so the presence of any Ni-Ti intermetallic phases is not stated.

Synthesis of the Nanocrystalline/Nanosized NiFe2O4 Powder by Ceramic Method and Mechanical Milling

2012 ◽  
Vol 188 ◽  
pp. 27-30 ◽  
Author(s):  
Vasile Florin Tarța ◽  
Ionel Chicinaş ◽  
Traian Florin Marinca ◽  
Bogdan Viorel Neamţu ◽  
Florin Popa ◽  
...  
Keyword(s):  
Milling Time ◽  
High Energy ◽  
Milling Process ◽  
X Ray Diffraction ◽  
Polycrystalline Nickel ◽  
Powder Morphology ◽  
Chemical Homogeneity ◽  
Ceramic Method ◽  
X Ray ◽  
Nanometric Range

The polycrystalline nickel ferrite - NiFe2O4has been obtained by ceramic route starting from a stoichiometric mixture of oxides (NiO and α-Fe2O3powders). The obtained NiFe2O4was subjected to high energy ball milling. The formation of NiFe2O4by ceramic method and also the evolution of the powder during milling were studied by X-ray diffraction. The mean crystallite size of the NiFe2O4continuously decreases with the increasing of the milling time and for all the milling time it is in nanometric range. The particles sizes are drastically reduced by milling process. For the milled samples, the particles size is ranging from tens of microns to few nanometers. The powder morphology and local chemical homogeneity were investigated by scanning electron microscopy (SEM) and respectively by energy dispersive x-ray spectrometry (EDX).

Mechanochemical Processes in the System “Titanium - Heptane” during Ball Milling

2020 ◽  
Vol 989 ◽  
pp. 532-536
Author(s):  
Olga M. Kanunnikova ◽  
V.V. Aksenova ◽  
G.A. Dorofeev
Keyword(s):  
Ball Milling ◽  
Milling Time ◽  
High Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Liquid Phases ◽  
Crystallite Sizes ◽  
Ft Ir ◽  
Titanium Powders ◽  
Ft Ir Spectroscopy

The transformations of the solid and liquid phases at high energy planetary ball milling of heptane together with titanium powder were investigated. The sequence of structural heptane transformations using UV-and FT-IR spectroscopy was investigated. Phase constitutions of ball milled titanium powders were studied by X-ray diffraction. It is shown that mechanically induced destruction of heptane occurs by the mechanism of catalytic cracking. The main solid products of the mechanosynthesis were hexagonal (HCP) and cubic (FCC) titanium carbohydrides. Evolution of lattice parameters, crystallite sizes, and micro-stresses of the solid phases during ball milling as a function of the ball milling time have been discussed.

Effects of Neutron and Electron Irradiation on 4H-SiC Diodes

2016 ◽  
Vol 840 ◽  
pp. 281-286 ◽  
Author(s):  
Yusof Abdullah ◽  
Cik Rohaida Che Hak ◽  
Megat Harun Al Rashid Megat Ahmad ◽  
Nurul Fadzlin Hasbullah ◽  
Mohd Reusmaazran Yusof ◽  
...  
Keyword(s):  
Neutron Fluence ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Lattice Strains ◽  
Atomic Force ◽  
Crystallite Sizes ◽  
Current Characteristics ◽  
Sem Morphology

4H-SiC Schottky barrier diodes (SBDs) were irradiated to neutron fluence of 3.55 x1016 cm-2 and 6.6 x 1015 cm-2 (15,000 kGy) electrons respectively. In general, characterization of the irradiated samples show that the current characteristics of the diodes decreased. The performance of Schottky gate contact is less for electron irradiated sample compared to neutron irradiated sample. The d-spacing, crystallite sizes and lattice strains were calculated from X-ray diffraction (XRD) measurements. SiC Schottky interface damage and radiation defects, as observed in atomic force microscopy (AFM) topography and scanning electron microscope (SEM) morphology images is possibly the main reason for this reduction in performance.

scholarly journals Analysis of the influence of β-TCP particle size on deagglomeration processes

2020 ◽  
Vol 9 (4) ◽  
pp. e175943067
Author(s):  
João Augusto Martins Almeida ◽  
Bruna Horta Bastos Kuffner ◽  
Gilbert Silva ◽  
Patrícia Capellato ◽  
Daniela Sachs
Keyword(s):  
Particle Size ◽  
Ball Milling ◽  
High Energy ◽  
Milling Process ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Powder Morphology ◽  
Heterogeneous Distribution ◽  
X Ray ◽  
Energy Ball

There are a class of material widely used in bone tissue repair. This material is calcium phosphate ceramics (CPCs)that can be used on two phases: α and β. However, β-TCP is more used in bone regeneration than α–TCP due to the biocompatible and bioactive properties.In the present work evaluate the influence of these two distinct processes to deagglomeration and the consequence in the particle size of the β-TCP obtained through solid-state reaction. Among all of the routes used in research and industry to reduce the particles size of different materials, the high energy ball milling is one of the most effective, due to the high rotation speed that this process achieves. The deagglomeration through agate mortar is considered a cheaper process when compared with the high energy ball milling. The characterization of both powders, deagglomerated in high energy ball milling and agate mortar, was realized through scanning electron microscopy, to analyze the powder morphology, and laser granulometry, to determine the size of the particles. Also, the forerunner powder was previously submitted to x-ray diffraction to confirm the formation of the β-TCP phase. The analysis through x-ray diffraction confirmed that the phase formed during the calcination process corresponded to the β-TCP. The results obtained after the deagglomeration processes indicated that the morphology was predominantly irregular for both powders. In relation to the granulometry, the deagglomeration performed through agate mortar showed to produce particles with smaller size (11,4µm e 0,9µm) and heterogeneous distribution, while the high energy ball milling process produced particles with larger size (11,4µm a 1,8µm) and higher homogeneity.

Characterizations of Synthetic 8mol% YSZ with Comparison to 3mol %YSZ for HT-SOFC

2020 ◽  
Vol 38 (4A) ◽  
pp. 491-500
Author(s):  
Abeer F. Al-Attar ◽  
Saad B. H. Farid ◽  
Fadhil A. Hashim
Keyword(s):  
Ionic Conductivity ◽  
Electrochemical Impedance ◽  
Structural Information ◽  
Impedance Analysis ◽  
High Energy ◽  
Yttria Stabilized Zirconia ◽  
X Ray Diffraction ◽  
Stabilized Zirconia ◽  
Powder Morphology ◽  
X Ray

In this work, Yttria (Y2O3) was successfully doped into tetragonal 3mol% yttria stabilized Zirconia (3YSZ) by high energy-mechanical milling to synthesize 8mol% yttria stabilized Zirconia (8YSZ) used as an electrolyte for high temperature solid oxide fuel cells (HT-SOFC). This work aims to evaluate the densification and ionic conductivity of the sintered electrolytes at 1650°C. The bulk density was measured according to ASTM C373-17. The powder morphology and the microstructure of the sintered electrolytes were analyzed via Field Emission Scanning Electron Microscopy (FESEM). The chemical analysis was obtained with Energy-dispersive X-ray spectroscopy (EDS). Also, X-ray diffraction (XRD) was used to obtain structural information of the starting materials and the sintered electrolytes. The ionic conductivity was obtained through electrochemical impedance spectroscopy (EIS) in the air as a function of temperatures at a frequency range of 100(mHz)-100(kHz). It is found that the 3YSZ has a higher density than the 8YSZ. The impedance analysis showed that the ionic conductivity of the prepared 8YSZ at 800°C is0.906 (S.cm) and it was 0.214(S.cm) of the 3YSZ. Besides, 8YSZ has a lower activation energy 0.774(eV) than that of the 3YSZ 0.901(eV). Thus, the prepared 8YSZ can be nominated as an electrolyte for the HT-SOFC.

scholarly journals Optical, XPS and XRD Studies of Semiconducting Copper Sulfide Layers on a Polyamide Film

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Valentina Krylova ◽  
Mindaugas Andrulevičius
Keyword(s):  
Photoelectron Spectroscopy ◽  
Copper Sulfide ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Xrd Studies ◽  
Polyamide Film ◽  
Indirect Band Gap ◽  
Xrd Method

Copper sulfide layers were formed on polyamide PA 6 surface using the sorption-diffusion method. Polymer samples were immersed for 4 and 5 h in 0.15 mol⋅  solutions and acidified with HCl (0.1 mol⋅) at . After washing and drying, the samples were treated with Cu(I) salt solution. The samples were studied by UV/VIS, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. All methods confirmed that on the surface of the polyamide film a layer of copper sulfide was formed. The copper sulfide layers are indirect band-gap semiconductors. The values of are 1.25 and 1.3 eV for 4 h and 5 h sulfured PA 6 respectively. Copper XPS spectra analyses showed Cu(I) bonds only in deeper layers of the formed film, while in sulfur XPS S 2p spectra dominating sulfide bonds were found after cleaning the surface with ions. It has been established by the XRD method that, beside , the layer contains as well. For PA 6 initially sulfured 4 h, grain size forchalcocite, , was  nm and fordjurleite, , it was 54.17 nm. The sheet resistance of the obtained layer varies from 6300 to 102 .

Local atomic structure in tetragonal pure ZrO2nanopowders

2010 ◽  
Vol 43 (2) ◽  
pp. 227-236 ◽  
Author(s):  
Leandro M. Acuña ◽  
Diego G. Lamas ◽  
Rodolfo O. Fuentes ◽  
Ismael O. Fábregas ◽  
Márcia C. A. Fantini ◽  
...  
Keyword(s):  
Tetragonal Phase ◽  
Local Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Atomic Structures ◽  
Crystallite Sizes ◽  
Exafs Study ◽  
The Difference ◽  
X Ray Absorption ◽  
Good Agreement

The local atomic structures around the Zr atom of pure (undoped) ZrO2nanopowders with different average crystallite sizes, ranging from 7 to 40 nm, have been investigated. The nanopowders were synthesized by different wet-chemical routes, but all exhibit the high-temperature tetragonal phase stabilized at room temperature, as established by synchrotron radiation X-ray diffraction. The extended X-ray absorption fine structure (EXAFS) technique was applied to analyze the local structure around the Zr atoms. Several authors have studied this system using the EXAFS technique without obtaining a good agreement between crystallographic and EXAFS data. In this work, it is shown that the local structure of ZrO2nanopowders can be described by a model consisting of two oxygen subshells (4 + 4 atoms) with different Zr—O distances, in agreement with those independently determined by X-ray diffraction. However, the EXAFS study shows that the second oxygen subshell exhibits a Debye–Waller (DW) parameter much higher than that of the first oxygen subshell, a result that cannot be explained by the crystallographic model accepted for the tetragonal phase of zirconia-based materials. However, as proposed by other authors, the difference in the DW parameters between the two oxygen subshells around the Zr atoms can be explained by the existence of oxygen displacements perpendicular to thezdirection; these mainly affect the second oxygen subshell because of the directional character of the EXAFS DW parameter, in contradiction to the crystallographic value. It is also established that this model is similar to another model having three oxygen subshells, with a 4 + 2 + 2 distribution of atoms, with only one DW parameter for all oxygen subshells. Both models are in good agreement with the crystal structure determined by X-ray diffraction experiments.

Determination of crystallinity of Chinese handmade papers by means of X-ray diffraction

2020 ◽  
Vol 41 (2) ◽  
pp. 69-86
Author(s):  
Peng Liu ◽  
Hongbin Zhang ◽  
Sinong Wang ◽  
Hui Yu ◽  
Bingjie Lu ◽  
...  
Keyword(s):  
Negative Influence ◽  
X Ray Diffraction ◽  
Cross Sectional ◽  
X Ray ◽  
Eulaliopsis Binata ◽  
Different Types ◽  
Powder Samples ◽  
Xrd Patterns ◽  
Xrd Method

AbstractThe crystallinity indices (CrI) of Chinese handmade papers were investigated using the X-ray diffraction (XRD) method. Four Chinese handmade papers, Yingchun, Zhuma, Yuanshu and Longxucao papers were used as model substrates of mulberry bark, ramie, bamboo and Eulaliopsis binata papers, respectively. Two forms of the paper samples, paper sheets and their comminuted powders, were used in this study. The results showed that their XRD patterns belong to the cellulose-I type and Iβ dominates the cellulose microstructure of these paper samples. Moreover, it was found that the microstructures and CrIs of cellulose of these papers were changed by the grinding treatment. This work suggested that the sheet form of the handmade papers is suitable to determine CrI by XRD, despite the contribution of non-cellulosic components in the papers. The order of CrIs for these paper sheet samples was Yingchun, Zhuma, Longxucao and Yuanshu papers. Besides CrIs, differences in cross-sectional areas of the crystalline zone of cellulose can be used for comparing different types of handmade papers. It was also found that the CrIs and crystallite size of paper cellulose varied between the sheet samples and the powder samples, illustrating that the pulverisation has a negative influence on the microstructure of the handmade papers.

Effect of Synthesis Temperature on Particles Size and Morphology of Zirconium Oxide Nanoparticle

2017 ◽  
Vol 50 ◽  
pp. 18-31 ◽  
Author(s):  
Rudzani Sigwadi ◽  
Simon Dhlamini ◽  
Touhami Mokrani ◽  
Patrick Nonjola
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Zirconium Oxide ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Crystallite Sizes ◽  
Ft Ir

The paper presents the synthesis and investigation of zirconium oxide (ZrO2) nanoparticles that were synthesised by precipitation method with the effects of the temperatures of reaction on the particles size, morphology, crystallite sizes and stability at high temperature. The reaction temperature effect on the particle size, morphology, crystallite sizes and stabilized a higher temperature (tetragonal and cubic) phases was studied. Thermal decomposition, band structure and functional groups were analyzed by Brunauer-Emmett-Teller (BET), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA) and Fourier transform infrared (FT-IR). The crystal structure was determined using X-ray diffraction. The morphology and the particle size were studied using (SEM) and (TEM). The shaped particles were confirmed through the SEM analysis. The transmission electron microscopic analysis confirmed the formation of the nanoparticles with the particle size. The FT-IR spectra showed the strong presence of ZrO2 nanoparticles.

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