Papers by Keyword: Diffusion

Abstract: It is shown that investigations of the isotope exchange kinetics in nanocrystalline oxides allows one not only to solve problems connected with determination of process parameters and characteristic scenarios, but also to substantially extend experimental opportunities in analysis of diffusion properties of oxides. A specific behavior of the oxygen isotope exchange was studied in nanocrystalline LaMnO3 and ZrO2:Y2O3 oxides. The former oxide is characterized by very small values of oxygen volume diffusion coefficients, while the latter one is, on the contrary, an ionic conductor. The study was carried out using powdered nanomaterials prepared from original ceramic materials by grinding in planetary mills or by laser evaporation. The study revealed future trends in the use of nanomaterials for analysis of the diffusion kinetics in oxides. It is demonstrated that in this case the sensitivity of traditional isotope methods increases considerably and fundamentally new opportunities are provided for analysis of processes on the "gas phase  solid state" interface as well as for the study of volume diffusion in polycrystals. Considering a strong dependence of the isotope exchange rate on the particle size, it is also topical to conduct studies dealing, along with determination of kinetic parameters of the process, with the use of the obtained data for certification of dimensional characteristics of oxide nanopowders.

Abstract: Recently, there has been a great deal of interest in the properties of hollow nanoparticles for use in advanced technologies. The diffusion phenomenon known as the Kirkendall effect features in one of the important experimental methods of synthesis of hollow binary nanoparticles. Diffusion naturally features prominently in shrinkage mechanisms of hollow nanoparticles. In this paper, we summarize the progress made so far in understanding the formation and shrinkage by diffusion processes of hollow nanoparticles and their apparent stability.

Abstract: Chemical vapor deposition (CVD) diamond thin films are widely used in modern industries. However, due to the nature of polycrystalline, thin films are required to be polished in the final process to increase its surface quality. Thermal-chemical polishing is known for its less processing time and low cost. In this paper, the experiments are carried out to observe the effect of processing conditions such as temperature, rotational speed, polishing pressure, and substrate material on the surface roughness and on the material removal rate of the chemical vapor deposition diamond (CVDD). At the same time, the processing mechanism for this thermal-chemical polishing is investigated, and a polishing model is built for comparison with the experiment results. The results show that the material removal rate is affected mainly by the diffusing rate in the Fe-C polishing system. By using the model, the approximate value of material removal rate can be calculated according to the polishing temperature.

Abstract: The aluminum depletion of NiCrAlY bond coat in an air-plasma-sprayed thermal barrier coating (TBC) has been studied by experimental and simulative approaches. Upon thermal exposure, Al depletion regions were observed. The depletion of aluminum is resulting from Al diffusion towards the surface of bond coat and into substrate. A mathematical model of Al depletion was presented. The model is able to explain the observed results in a qualitative way and has been shown that Al depletes within the bond coat by diffusion.

Abstract: Chitosan (an aminopolysaccharide), cross-linked with glutaraldehyde, is very efficient for Pd(II) and Pt(IV) recovery from acidic solutions (pH 2). Due to poorly porous properties, it is necessary to condition the biopolymer as hydrogels. The uncontrolled drying of hydrogels depreciates the diffusion properties of original materials. A different method (to the acidic dissolving/alkaline neutralization procedure) has been used: after chitosan dissolving in acetic acid solution, the viscous solution was dropped into an ionotropic gelling solution (polyphosphate and glutaraldehyde to form stable gel beads with improved porosity. The restriction of diffusion properties due to drying step was less drastic with the modified procedure: a few hours were sufficient for reaching equilibrium while more than two days were required for standard material

Abstract: Crack disappearance by high-temperature oxidation was studied in alumina (Al2O3) composites toughened by Ni nanoparticles. This process is performed in air at temperature ranging from 1000 to 1300°C for 1 to 48 h. The results showed that crack disappearance depends on both annealing temperature and time. Complete crack disappearance in this composite was confirmed at lower temperatures for long oxidation period, 1100oC for 48 h, and higher temperature for shorter time, 1300oC for 1 h in air. The crack disappearance mechanism was explained on the basis of the formation of NiAl2O4 spinel on sample surfaces produced by the oxidation reaction during the heat treatment.

Abstract: Jump frequencies of Cd tracer atoms were measured in three phases having the orthorhombic Al11R3 structure, with R= La, Ce, or Pr. The structure has four inequivalent Al-sites and two inequivalent R-sites. 111In/Cd tracer atoms were observed to occupy several sites via the nuclear quadrupole interaction using perturbed angular correlation of gamma rays (PAC). Time-domain PAC spectra became damped as the temperature increased, which is attributed to nuclear relaxation caused by diffusional jumps of Cd tracer atoms leading to changes in orientations and/or magnitudes of electric field gradients (EFG’s). Maximum relaxations were observed near 770 K. A method is proposed for estimating the mean jump frequency at that temperature, giving a mean jump frequency w averaged over all sites of about 100 MHz. At still higher temperatures, damping decreased due to motional averaging, and the quadrupole perturbations evolved into unique signals having lower frequencies and corresponding in each phase to the averages of EFG tensors of all sites visited by the Cd tracer atoms. For Al11La3, the jump frequency at 1073 K was estimated to be 1.9 GHz. Such jump frequencies imply unusually high diffusivities in these phases.

Abstract: The insertion and diffusion energies of oxygen in presence of vacancies in nickel are studied by using the first-principle projector augmented waves (PAW). When the oxygen atom is located in a substitution site, the formation of a vacancy-oxygen pair is observed. Furthermore, we show that the formation of divacancies allows the oxygen atom to migrate more easily in the metal. A model for the migration process of the three-defect system is proposed. Finally, thermal expansion effects are included in our study; it is shown that temperature effects emphasize the diffusion.

Abstract: We present results of the molecular dynamics study of Al selfdiffusion, Al and Fe diffusion in Al-Fe dilute alloys. We found that addition of Fe does not change the vacancy formation energy but considerably slows down Al diffusion. We also found that Al and Fe migration energies, i.e. energies of vacancy exchange with Al and Fe atoms, differ very strongly. Both activation energies for Al and Fe diffusion are in satisfactory agreement with available experimental data.

Abstract: Jump frequencies of Cd tracer atoms were measured in three lanthanide gallides having the L12 structure: DyGa3, ErGa3 and LuGa3. 111In/Cd impurity probe atoms were observed to occupy the non-cubic Ga-sites through the nuclear quadrupole interaction using the method of perturbed angular correlation of gamma rays (PAC). Measurements at elevated temperatures exhibited nuclear relaxation (damping) of quadrupolar perturbation functions attributed to diffusional jumps of the probes among orientationally inequivalent Ga-sites. Accurate values of jump frequencies were determined from fits of the measured perturbation functions using a model of stochastically fluctuating electric-field gradients, as in previous work [e.g., Matthew O. Zacate, Aurélie Favrot and Gary S. Collins: Physical Review Letters Vol. 92 (2004) p. 225901]. Arrhenius plots of jump frequencies for the three systems exhibited jump-frequency activation enthalpies in the range 0.86-1.05 eV and prefactors of about 2 THz. The activation enthalpy for ErGa3, 0.86(2) eV is compared with those for ErAl3, 1.40(4) eV, and ErIn3, 1.34(5) eV.