Grain-boundary diffusion and solubility of helium in submicrocrystalline palladium

The diffusion and solubility of helium in palladium with a submicrocrystalline structure are investigated by thermal desorption of helium from He-saturated specimens at temperatures T = 293–508 K and saturation pressures P = 0.1–35 MPa. As the saturation pressure rises, the effective diffusion coefficient increases, exhibits a plateau, and then decreases to its initial value. Along with the four plateaus discovered earlier, the solubility versus saturation pressure dependence in the range 25.5–35.0 MPa demonstrates a fifth plateau, where the solubility is as high as (3.0 ± 0.4) × 10¹⁷ cm⁻³. It is shown that the helium diffuses along grain boundaries, at which clusters (traps) consisting of eight to ten vacancies are localized, and dissolves in these clusters. The high value of C _eff in the fifth plateau is explained by pairwise merging of adjacent vacancy clusters. From the D _eff(P) dependences, the vacancy clusters concentration is estimated as C* = 2.32 × 10¹⁶ cm⁻³. Within the experimental error, this value coincides with that obtained from the solubility data. Calculations of the energy of helium-defect interaction in submicrocrystalline Pd that are made using the molecular dynamics method support the experimental results.     

Mass-spectroscopic study of the diffusion and solubility of helium in submicrocrystalline palladium

By the method of helium thermal desorption from submicrocrystalline palladium presaturated in the gaseous phase, the diffusion coefficient D _eff and solubility coefficient C _eff of helium are measured in the range P=0–3 MPa and T=293–508 K. The pressure dependence of C _eff flattens at high pressures. At low saturation pressures, the temperature dependences of the diffusion and solubility coefficients may be divided into (1) high-temperature (400–508 K) and (2) low-temperature (293–400 K) ranges described by the exponentials D _{1, 2}=D ₀exp (−E _{1, 2} ^D /kT) and C _{1, 2}=C ₀exp (−E _{1, 2} ^S /kT). The energies of diffusion activation are E ₂ ^D =0.0036±0.0015 eV and E ₁ ^D =0.33±0.03 eV, and the solution energies are E ₂ ^S =−0.025±0.008 eV and E ₁ ^S =0.086±0.008 eV in the low-and high-temperature ranges, respectively. Mechanisms behind the diffusion and solution of helium are discussed.     

Creep and diffusion parameters in submicrocrystalline metals

We have studied the creep of nickel and copper in a submicrocrystalline (SMC) state in a vacuum and in the presence of a diffusion contact with an impurity (Cu and Al, respectively). It is shown that a reduction of the resistance in the presence of a diffusion contact with an impurity is observed in the SMC materials in the temperature range 398 to 473 K. This range is 200 to 400 K lower than the corresponding range for coarse-grained material. It is shown that in this temperature interval the coefficients of grain boundary diffusion for copper in SMC nickel are 5 to 6 orders of magnitude larger than in the coarse-grained material. We propose that the reduction in the temperature for the manifestation of a creep activation effect in the presence of a diffusion contact with an impurity in SMC materials is caused by the increase in the diffusion permeability of the submicrocrystalline grain boundaries. Institute of Materials and Strength Physics, Siberian Branch of the Russian Academy of Sciences. Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 3, pp. 77–82, March, 1998.     

Mass spectrometric investigation of low-temperature diffusion and solubility of helium in lead fluoride crystals

Thermal desorption of helium from presaturated crystals was used for mass spectrometric investigations of the diffusion and solubility of helium in lead fluoride crystals in the temperature range 606–714K which precedes the transition of the crystal to the superionic state. The experimental apparatus and measurement method are described and mechanisms for the diffusion and solubility of helium in PbF₂ are discussed. Zh. Tekh. Fiz. 68, 85–89 (December 1998)     

Helium defectoscopy of cerium gadolinium ceramics Ce0.8Gd0.2O1.9 with a submicrocrystalline structure in the impurity disorder region

The concentration of impurity anion vacancies formed upon the dissociation of gadolinium-vacancy complexes has been determined using helium defectoscopy of the cerium gadolinium ceramics Ce_0.8Gd_0.2O_1.9 with a submicrocrystalline structure in the temperature range T = 740–1123 K and at saturation pressures ranging from 0.05 to 15 MPa. It has been found that the energy of dissociation of gadoliniumvacancy complexes is E _eff ^D = 0.26 ± 0.06 eV, and the energy of dissolution of helium in anion vacancies in the impurity disorder region is E ^P = ?0.31 ± 0.09 eV. The proposed mechanism of dissolution has been confirmed by the investigation of the electrical conductivity of the cerium gadolinium ceramics, as well as by the high-speed molecular dynamics simulation of the dissociation of gadolinium-vacancy complexes. It has been assumed that a decrease in the effective dissolution energy in comparison with the results of the previously performed low-temperature investigations is caused by the mutual repulsion of vacancies formed upon the dissociation of gadolinium-vacancy complexes in highly concentrated solutions of gadolinium in CeO₂ with increasing temperature.     

Low-temperature helium defectoscopy and interaction of helium with ions of cerium gadolinium ceramics Ce<Subscript>0.8</Subscript>Gd<Subscript>0.2</Subscript>O<Subscript>1.9</Subscript> with a submicrocrystalline structure

The concentration of unbound neutral anion vacancies in cerium gadolinium ceramics Ce_0.8Gd_0.2O_1.9 with a submicrocrystalline structure has been determined using low-temperature helium defectoscopy at temperatures ranging from 613 to 773 K and at saturation pressures from 0.05 to 12 MPa. It has been found that the energy of dissociation of impurity-vacancy complexes is 1.1 ± 0.2 eV, and the energy of dissolution of helium in defects is −0.8 ± 0.2 eV. The obtained results have been compared both with the experimental data on the energy of interaction between helium and ions of the cerium gadolinium ceramics and with the results of the quantum-chemical calculations. It has been demonstrated that the anomalously low value of the energy of helium dissolution in the studied ceramic samples is determined by the chemical interaction of helium with the nearest environment of the cerium cations.     

The low-temperature solubility of helium in quartz

Technical Physics - The solubility of helium in α- and β-quartz single crystals, optical quartz crystals, and Pyrex glass has been studied by the method of thermal desorption of helium...     

The influence of defects in the crystal structure on helium diffusion in quartz

The solubility and diffusion of helium in quartz crystals are investigated as functions of the distribution and density of structural defects. The types of defects in the crystals are identified and their distribution over growth sectors is determined by x-ray diffraction topography and phase radiography with a synchrotron radiation source. The effective solubility and effective diffusion coefficients for helium in quartz are estimated from the experimental data on the amount of helium extracted from samples with different contents of defects. It is revealed that the effective diffusion coefficient of helium depends on the number of dislocations.     

Atomistics of helium diffusion in copper and tungsten

Using previously determined interatomic potentials, the activation energy for migration of a single substitutional helium atom in copper and tungsten has been determined. The mechanism of migration involves the jump of the helium atom out of the vacancy concurrent with the jump of a host atom into that vacancy. The helium then occupies the vacant site created by the jumping host atom, resulting in a substitutional helium at a distance of √2 r ₀ (√3r ₀) from its original site in copper (tungsten). The rate-limiting step in the process is found to be the jump of the helium out of the vacancy, the activation energy for which is 2.15 eV in copper and 4.69 eV in tungsten.     

Deformation behavior,strength, and plasticity of titanium with a submicrocrystalline structure formed under warm rolling

The temperature-deformation regimes of warm rolling through profiled rolls providing production of submicrocrystalline titanium are determined. For the obtained submicrocrystalline titanium, the annealing conditions under which internal stresses decrease and plasticity increases while maintaining high-strength submicrocrystalline structure are found. The data on the microstructure, deformation behavior, elastic-plastic properties, and the type of fracture of rods with submicrocrystalline structure are reported.     

Spin structure of antiprotonic helium in a magnetic field

The spin structure of the (37,35) energy level of antiprotonic helium-4 in permanent homogenous external magnetic field has been calculated in first order of perturbation theory. For weak magnetic fields the effect is observed as an additional broadening of the spectral lines. For magnetic fields of the order of kG and higher, the magnetic and hyperfine interactions become comparable to each other, and the hyperfine spectrum is rearranged.     

Study of the grain-boundary structure in submicrocrystalline niobium after equal-channel angular pressing

The method of Mössbauer emission spectroscopy on ^119m Sn nuclei was used to study grain boundaries in submicrocrystalline Nb produced by the method of equal-channel angular pressing (ECAP) of poly-crystalline Nb (99.9%). ECAP included 16 passes at room temperature.     

Thermophysical properties of PLZT ferroelectric ceramics with a nanopolar structure

The heat capacity, thermal expansion coefficient, and deformation of the PLZT-9/65/35 compound are studied in the temperature range 150–800 K. Diffuse anomalies are detected in the temperature dependences of the heat capacity and thermal expansion coefficient over wide temperature ranges of 250–650 and 330–550 K, respectively. The anomalous behavior of the heat capacity in the temperature range 250–650 K is shown to be caused by the appearance of two-level states (Schottky anomaly). The results obtained are discussed along with the data of structural and dielectric studies.     

Hyperfine structure in hydrogen and helium ion

QED theory of the hyperfine splitting of the 1s and 2s state in hydrogen isotopes and helium-3 ion is considered. We develop an accurate theory of a specific difference 8E_HFS(2s)−E_HFS(1s). We take into account higher-order QED and nuclear structure effects. In particular, we found the vacuum polarization contribution in order α(Zα)³E_F and examined the recoil contribution in order (Zα)³m/M and thus completed a calculation of the fourth order QED corrections. The higher-order nuclear structure contributions were also analysed. The theoretical predictions reported here are now of a higher accuracy than the experiment. The study of the difference provides the most accurate test (at a level of a part in 10⁸) of the QED theory of ns HFS up to date. The theory agrees with most of the experimental data.     

Ion transport and diffusion in nanocrystalline and glassy ceramics

In the present paper we review experimental studies on ion transport and diffusion in nanocrystalline and glassy ceramics of LiNbO₃ and LiAlSi₂O₆ and report on new ones on LiBO₂ using the measurement of dc conductivities and ⁷Li nuclear magnetic resonance spin-lattice relaxation rates. Nanocrystalline ceramics, with an average particle size of 50 nm and less, often show an enhanced diffusivity compared to their microcrystalline (μm-sized) counterparts. This increase is due to the large fraction of atoms or ions located in the interfacial regions. A key for understanding the structure-mobility relations in nanocrystalline ceramics is to clarify the microscopic structure of the grain boundaries and also the morphology of the grain boundary network. In this context it is useful to study not only the ion transport properties of the nano- and microcrystalline materials but also those of the corresponding glassy forms. Such comparative studies gave strong evidence that in some cases the interfacial regions are of amorphous structure. For example, this was recently shown for nanocrystalline lithium niobate which was prepared by high-energy ball milling.     

Mechanodynamic diffusion of helium atoms into porous copper

Mechanodynamic penetration of helium atoms into porous copper compressively strained at 4.2 K is studied. Porous copper is obtained by vaporizing zinc out of brass in vacuum at a temperature of 800°C for 8 h. The number of helium atoms which penetrated into the sample increased monotonically with strain to reach 2.9 × 10¹⁶ atoms/cm² at ? = 42%. This amount of helium is two and even more orders of magnitude larger than that obtained from the data available thus far on mechanodynamic penetration of atoms of an external medium into crystalline and amorphous materials under strain. The relations obtained suggest that specific types of helium traps determine the kinetics of mechanodynamic diffusion of helium into solids.     

Diffusion and solubility of helium in lead fluoride single crystals in the superionic transition region

Temperature curves of the diffusion coefficients and solubilities of helium in pure and holmium-doped lead fluoride crystals are obtained in the superionic phase-transition range. Possible mechanisms of the interaction of helium with ions are discussed, along with mechanisms of the solubility and diffusion of helium in a crystal. Fiz. Tverd. Tela (St. Petersburg) 40, 759–760 (April 1998)     

微晶结构对氟氧化物玻璃陶瓷发光特性的影响

制备了成分相同的Er3+/Yb3+共掺氟氧化物玻璃和氟氧化物玻璃陶瓷样品，x射线衍射谱和荧光光谱表明热处理后玻璃陶瓷中形成了纳米结构的微晶，根据Judd Ofelt理论计算和差热曲线分析，证实稀土离子掺入PbF2微晶中.分别计算了热处理前后微晶态部分在玻璃体中所占的比例. 关键词： 微晶结构 玻璃陶瓷 荧光光谱     

Changes in the diffusion properties of nonequilibrium grain boundaries upon recrystallization and superplastic deformation of submicrocrystalline metals and alloys

The effect of an increase in the coefficient of the grain-boundary diffusion upon recrystallization and superplastic deformation of submicrocrystalline (SMC) materials prepared by severe plastic deformation has been studied. It is shown that the coefficient of the grain-boundary diffusion of the SMC materials is dependent on the intensity of the lattice dislocation flow whose value is proportional to the rate of the grain boundary migration upon annealing of SMC metals or the rate of the intragrain deformation under conditions of superplastic deformation of SMC alloys. It is found that, at a high rate of grain boundary migrations and high rates of superplastic deformation, the intensity of the lattice dislocation flow bombarding grain boundaries of SMC materials is higher than the intensity of their diffusion accommodation, which leads to an increase in the coefficient of the grain-boundary diffusion and a decrease in the activation energy. The results of the numerical calculations agree well with the experimental data.