scholarly journals The effect of antimony presence in anodic copper on kinetics and mechanism of anodic dissolution and cathodic deposition of copper

2008 ◽  
Vol 44 (1) ◽  
pp. 107-114 ◽  
Author(s):  
Z.D. Stankovic ◽  
V. Cvetkovski ◽  
M. Vukovic
Keyword(s):  
Anodic Dissolution ◽  
Single Pulse ◽  
Pulse Method ◽  
Sulfate Solution ◽  
Electrode Reaction ◽  
Xrd Analysis ◽  
Lattice Parameter ◽  
Crystal Lattice Parameter ◽  
Cathodic Deposition ◽  
Anode Copper

The influence of the presence of Sb atoms, as foreign metal atoms in anode copper, on kinetics, and, on the mechanism of anodic dissolution and cathodic deposition of copper in acidic sulfate solution has been investigated. The galvanostatic single-pulse method has been used. Results indicate that presence of Sb atoms in anode copper increase the exchange current density as determined from the Tafel analysis of the electrode reaction. It is attributed to the increase of the crystal lattice parameter determined from XRD analysis of the electrode material.

scholarly journals The effect of bi presence as impurities in anodic copper on kinetics and mechanism of anodic dissolution and cathodic deposition of copper

2010 ◽  
Vol 64 (4) ◽  
pp. 337-342
Author(s):  
Zvonimir Stankovic ◽  
Vladimir Cvetkovski ◽  
Vesna Grekulovic
Keyword(s):  
Anodic Dissolution ◽  
Single Pulse ◽  
Pulse Method ◽  
Sulfate Solution ◽  
Electrode Reaction ◽  
Xrd Analysis ◽  
Kinetics And Mechanism ◽  
Crystal Lattice Parameter ◽  
Cathodic Deposition ◽  
Anode Copper

The influence of Bi, as foreign metal atoms in anode copper, on kinetics and mechanism of anodic dissolution and cathodic deposition of copper in acidic sulfate solution was investigated using the galvanostatic single-pulse method. Results indicate that presence of Bi atoms in anode copper increases the exchange current density, as determined from the Tafel analysis of the electrode reaction, which is attributed to the increase of the crystal lattice parameter determined from XRD analysis of the electrode material.

Structure and properties of rails after extremely long-term operation

2020 ◽  
pp. 30-39 ◽  
Author(s):  
Yu. F. Ivanov ◽  
V. E. Gromov ◽  
V. E. Kormyshev ◽  
A. M. Glezer
Keyword(s):  
Surface Layer ◽  
Lattice Parameter ◽  
Crystal Lattice Parameter ◽  
Subgrain Structure ◽  
Structure And Properties ◽  
Term Operation ◽  
Head Section ◽  
Structure Phase ◽  
Defective Surface

The paper reveals regularities and mechanisms of structure-phase states and properties formation of of differentially hardened 100-m rails of DT 350 category after the passed tonnage of 1411 mln. tons brutto. The formation of highly defective surface layer with nanosize (40–50 nm) grain-subgrain structure of pearlite colonies and submicrocrystal (150–250 nm) structure grains with structure free ferrite is detected. The change of hardness, microhardness, crystal lattice parameter, microdistorsion level, scalar and excess dislocation density on the rails head section are analyzed. The possible mechanisms of cementite plates’ transformation at extremely long-term operation are discussed.

Peierls “Washboard” Controls Dynamics of the Domain Walls in Molecular Ferrimagnets

2015 ◽  
Vol 233-234 ◽  
pp. 55-59
Author(s):  
Marina Kirman ◽  
Artem Talantsev ◽  
Roman Morgunov
Keyword(s):  
Domain Wall ◽  
Crystal Lattice ◽  
Domain Walls ◽  
Low Frequency ◽  
Domain Wall Motion ◽  
Lattice Parameter ◽  
Structural Defects ◽  
Crystal Lattice Parameter ◽  
Wall Width ◽  
Debye Relaxation

The magnetization dynamics of metal-organic crystals has been studied in low frequency AC magnetic field. Four modes of domain wall motion (Debye relaxation, creep, slide and over - barrier motion (switching)) were distinguished in [MnII(H(R/S)-pn)(H2O)] [MnIII(CN)6]⋅2H2O crystals. Debye relaxation and creep of the domain walls are sensitive to Peierls relief configuration controlled by crystal lattice chirality. Structural defects and periodical Peierls potential compete in the damping of the domain walls. Driving factor of this competition is ratio of the domain wall width to the crystal lattice parameter.

scholarly journals The Effect of High-Intensity Electron Beam on the Crystal Structure, Phase Composition, and Properties of Al–Si Alloys with Different Silicon Content

2021 ◽  
Vol 22 (1) ◽  
pp. 129-157
Author(s):  
D. V. Zaguliaev ◽  
S. V. Konovalov ◽  
Yu. F. Ivanov ◽  
V. E. Gromov ◽  
V. V. Shlyarov ◽  
...  
Keyword(s):  
Solid Solution ◽  
Electron Beam ◽  
Phase Composition ◽  
Crystal Lattice ◽  
High Intensity ◽  
Materials Science ◽  
Lattice Parameter ◽  
Crystal Lattice Parameter ◽  
Material Surface ◽  
Modified Layer

The study deals with the element–phase composition, microstructure evolution, crystal-lattice parameter, and microdistortions as well as the size of the coherent scattering region in the Al–10.65Si–2.11Cu and Al–5.39Si–1.33Cu alloys irradiated with the high-intensity electron beam. As revealed by the methods of x-ray phase analysis, the principal phases in untreated alloys are the aluminium-based solid solution, silicon, intermetallics, and Fe2Al9Si2 phase. In addition, the Cu9Al4 phase is detected in Al–10.65Si–2.11Cu alloy. Processing alloys with the pulsed electron beam induces the transformation of lattice parameters of Al–10.65Si–2.11Cu (aluminium-based solid solution) and Al–5.39Si–1.33Cu (Al1 and Al2 phases). The reason for the crystal-lattice parameter change in the Al–10.65Si–2.11Cu and Al–5.39Si–1.33Cu alloys is suggested to be the changing concentration of alloying elements in the solid solution of these phases. As established, if a density of electron beam is of 30 and 50 J/cm2, the silicon and intermetallic compounds dissolve in the modified layer. The state-of-the-art methods of the physical materials science made possible to establish the formation of a layer with a nanocrystalline structure of the cell-type crystallization because of the material surface irradiation. The thickness of a modified layer depends on the parameters of the electron-beam treatment and reaches maximum of 90 µm at the energy density of 50 J/cm2. According to the transmission (TEM) and scanning (SEM) electron microscopy data, the silicon particles occupy the cell boundaries. Such changes in the structural and phase states of the materials response on their mechanical characteristics. To characterize the surface properties, the microhardness, wear parameter, and friction coefficient values are determined directly on the irradiated surface for all modification variants. As shown, the irradiation of the material surface with an intensive electron beam increases wear resistance and microhardness of the Al–10.65Si–2.11Cu and Al–5.39Si–1.33Cu alloys.

Effect of Ce-Mn Codoping on the Structural, Morphological and Electrical Properties of the BaTiO3 Based Ceramics

2021 ◽  
Vol 11 (4) ◽  
pp. 12215-12226
Keyword(s):  
Dielectric Constant ◽  
Electrical Properties ◽  
Doping Concentration ◽  
Xrd Analysis ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Stoichiometric Ratio ◽  
Co Doping ◽  
Mn Doped ◽  
Co Doped

Undoped, Cerium (Ce) doped, Manganese (Mn) doped and Ce-Mn co-doped Barium Titanate (BaTiO3) with the general formula Ba1-xCexMnyTi1-yO3 (where x = 0.00, 0.01, 0.02, 0.03, y = 0.00; x = 0.00, y =0.01, 0.02, 0.03; and x = y = 0.01, 0.02,0.03) were synthesized by solid-state reaction method and sintered at 1200 C for 4 hr with an aim to study their structural and electrical properties. The grain size of the samples has been estimated using the Scanning Electron Microscopy (SEM). The X-ray Diffraction (XRD) analysis indicates that the structure of the Ce-doped and Ce-Mn co-doped BaTiO3 is cubic. However, the undoped BaTiO3 and Mn-doped BaTiO3 confirmed the tetragonal-cubic mixed phases. With the change of doping concentrations, the positions of different peaks shifted slightly. The lattice parameter varied irregularly with increasing doping concentration because of Mn's changeable valency. EDX spectra confirmed the presence of Ba, Ti, Ce, and Mn contents in the co-doped samples with stoichiometric ratio. Crystallinity is observed to be clearly increased when Ce-Mn is co-doped in BaTiO3. J-V characteristic curves indicate transition from conducting to semiconducting nature for the doped and co-doped samples with the increase in temperature. The dielectric constant of the samples increases up to 4500 with the doping concentration. The higher values of dielectric constant are observed for the 2% Mn-doped and 1% Ce-Mn co-doped samples compared to the other undoped samples. For the undoped and Mn-doped samples, constant dielectric values increase with temperature but decrease for the Ce-doped and Ce-Mn co-doped samples. It is inferred that co-doping of BaTiO3 with Ce and Mn would be beneficial and economical for its applications.

scholarly journals Lattice Strain Analysis of a Mn-Doped CdSe QD System Using Crystallography Techniques

Processes ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 639 ◽  
Author(s):  
Hamizi ◽  
Johan ◽  
Ghazali ◽  
Wahab ◽  
Chowdhury ◽  
...  
Keyword(s):  
Lattice Strain ◽  
Reaction Times ◽  
Strain Analysis ◽  
Xrd Analysis ◽  
Lattice Parameter ◽  
Strain Effect ◽  
Similar Reaction ◽  
Cdse Qds ◽  
Particle Size Reduction ◽  
Mn Doped

In this work, we report on the different sizes of manganese-doped cadmium selenide quantum dots (Mn-doped CdSe QDs) synthesized for 0 to 90 min using a reverse micelle organic solvent method and surfactant having a zinc blende structure, with physical size varying from 3 to 14 nm and crystallite size from 2.46 to 5.46 nm and with a narrow size distribution. At similar reaction times, Mn-doped CdSe QDs displayed the growth of larger QDs compared with the pure CdSe QDs. Due to the implementation of lattice strain owing to the inclusion of Mn atoms in the CdSe QD lattice, the lattice parameter was compressed as the QD size increased. Strain was induced by the particle size reduction, as observed from X-ray diffractometer (XRD) analysis. The analyses of the strain effect on the QD reduction are discussed relative to each of the XRD characteristics.

scholarly journals Synthesis, Characterization, and Thermal Decomposition of Pure and Dysprosium Doped Yttrium Phosphate System

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
K. K. Bamzai ◽  
Nidhi Kachroo ◽  
Vishal Singh ◽  
Seema Verma
Keyword(s):  
Thermogravimetric Analysis ◽  
Ammonium Hydroxide ◽  
Xrd Analysis ◽  
Lattice Parameter ◽  
Energy Dispersive ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Structural Investigations ◽  
X Ray

Yttrium phosphate and dysprosium doped yttrium phosphate were synthesized from aqueous solutions using rare earth chloride, phosphoric acid, and traces of ammonium hydroxide. The synthesized material was then characterized for their structural investigations using powder X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM) supplemented with energy dispersive X-ray analysis (EDAX). The spectroscopic investigations were carried out using Fourier transform infrared (FTIR) spectroscopy. The thermal stability was studied using differential thermogravimetric analysis (DTA), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC) techniques. X-ray diffraction analysis reveals that both yttrium phosphate and dysprosium doped yttrium phosphate belong to tetragonal system with lattice parameter  Å,  Å and  Å,  Å, respectively. The stoichiometry of the grown composition was established by energy dispersive X-ray analysis. The EDAX analysis suggests the presence of water molecules. The presence of water molecules along with orthophosphate group and metallic ion group was confirmed by FTIR analysis. Thermogravimetric analysis suggests that decomposition in case of yttrium phosphate takes place in three different stages and the final product stabilizes after 706°C, whereas in case of dysprosium doped yttrium phosphate the decomposition occurs in two different stages, and the final product stabilizes after 519°C.

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