Polymorphism in Sr3Fe2O7−x

The compound Sr₃Fe₂O_7–x , with variable iron valence, was investigated by X-ray powder techniques, both at room and at high temperatures. If the material is examined in massive form, a single phase called -Sr₃Fe₂O_7–x appears as previously reported in the literature. This -phase is tetragonal and exhibits the lattice parameters: a=3.874 and c=40.314 Å. Two other phases, called and -Sr₃Fe₂O_7–x , respectively, can be obtained on heating the finely powdered material when laid on a flat platinum support. The form is stable up to 1275° C, while the form is revealed only above 1275° C and changes always into -Sr₃Fe₂O_7–x when quenched. Both and phases are tetragonal, with a=4.001 and c= 58.251 for the form and a=4.013, c=57.092 Å for the form. The transition involves a true phase equilibrium, while the transformation is possible only by means of a suitable mechanical treatment of the material.     

Thermal Expansion and Isothermal Compressibility of TlIn1 – xNdxSe2 (0 ≤ x≤ 0.08) Crystals

The thermal expansion coefficient () and isothermal compressibility ( _T ) of TlIn_{1 – x} Nd _x Se₂(0 x 0.08) crystals were measured between 77 and 400 K. In the range 77–160 K, both and _T increase with temperature, the increase in being much steeper. At higher temperatures, and _T change very little. The observed composition dependences of and _T are interpreted in terms of energy-band structure.     

Methanation of carbon deposited directly from CO2 on rhodium-bearing activated magnetite

Methanation reactivity was studied for the surface carbon deposited from CO₂ on the surface of Rh-bearing activated magnetite. The most active material (Rh=0.83 wt %) for methanation was prepared by the impregnation method at 60°C and showed 98% conversion at 300°C. The surface carbon was composed of elemental carbon (-carbon) and polymerized carbon (-carbon), the proportion being dependent on the density of carbon deposited. In temperature-programmed surface reaction, the extent of conversion of the - and -carbon to CH₄ was 0.34 (-carbon) and 0.53 (-carbon), respectively, and the total conversion was 0.87. This result indicates that not only elemental carbon but polymerized carbon (-carbon) could be converted to CH₄ on the Rh-bearing activated (-carbon) magnetite, whereas -carbon is not hydrogenated on activated magnetite.     

Investigations of the copper isotope effect in oxygen-deficient YBa2Cu3O7−δ

We present data on the copper isotope effect (⁶³Cu-⁶⁵Cu), C_u =-nT_c/nm_Cu, for two isotopic pairs of oxygen-deficient YBa₂Cu₃O_7–, where varies between 0.06 and 0.52. _Cu is below 0.01 at =0.06 (fully oxygenated), it takes values between –0.14 and –0.34 in the 60 K plateau. Larger negative values of _Cu are observed away from the plateau. The dependence of _Cu is similar to that of the pressure effect dnT_c/dP.     

The role of ε-martensite in the impact toughness of an Fe-17Mn alloy

The influence of -martensite on the cryogenic toughness of an Fe-17 wt% Mn alloy was studied in this work. Alloys were tempered at various temperatures in order to systematically increase the volume fraction of -martensite. This was followed by Charpy impact testing conducted at room temperature and at–196°C. The experimental results indicated that although room-temperature toughness was not influenced by the -martensite content, the cryogenic toughness was strongly dependent on the volume fraction of -martensite. In particular, with the exception of the alloys tempered at 400 and 450°C, the impact toughness consistently increased with -martensite content. Microstructural and fractographic evaluations using SEM and TEM suggested that the toughness improvements were attributed to the stress-induced martensite transformation. No microstructural evidence was found which could be ascribed to an effect of -martensite on the low-temperature embrittlement exhibited by Fe-Mn alloys tempered at 400–450°C.     

The crystal growth and thermoelectric properties of chromium disilicide

Single crystals of chromium disilicide about 8 mm in diameter and 35 mm long were grown using the floating zone technique. Measurements of electrical resistivity , Hall coefficient R and thermoelectric power were carried out in the temperature range from 85 to 1100 K. The values of and showed the anisotropy over the temperature range studied. The ratios parallel and perpendicular to the c-axis were / =1.9 and /=1.7 respectively, at room temperature. It was found to be a degenerate semiconductor having the hole concentration of 6.3×10²⁰ cm^–3 below 600 K. The effective masses of holes parallel and perpendicular to the c-axis determined from the thermoelectric power and the hole concentration near room temperature were estimated to be five and three times as large as a free electron mass, respectively. The calculation on the values of and was made using those effective masses. These values showed good agreement with the observed values in the temperature range from 150 to 1100 K.     

The occurrence of stress-induced α′ martensite in an (α+γ) Fe-Cr-Ni alloy

The interaction of an applied stress with the displacive shear during the martensitic transformation determined theK-S variants which formed in three types of tensile specimens, with tensile directions of 0°, 45° and 90° to a rolling direction respectively. The 3–6, 4–5 and 1–3 variants in a 0°-specimen, 1–5 and 4–5 variants in a 45°-specimen and 4-4 and 3–6 variants in a 90°-specimen are chosen asK-S variants which have the maximum value ofU/ in respective tensile directions. These variants are related to the occurrence of martensite with particular orientations as (100), (110) and (211).     

Specific Heat of LaMnO3 + δ at 50 K ≤ T ≤ 160 K

We have developed a shell model, which includes the long-range coulomb, van der Waals interaction, and the short-range Hafemeister–Flygare repulsive interaction operative up to second neighbor atom to study the cohesive and thermal properties of LaMnO_{3 +} . The results on cohesive energy obtained by us are in good agreement with that of calculated value by DeSouza et. al. (R. A. DeSouza, M. S. Islam, and E. I. Tiffee, J. Mater. Chem. 9, 1621 (1999)). In addition, we have also calculated molecular force constant (f), compressibility (), restrahlen frequency (_o), Debye temperature (_D), and the low temperature specific heat at 50 K T 160 K. Our results on Debye temperature and specific heat for the temperature range 50 K T 160 K are closer to the recently measured data with an automated quasi-adiabatic pulse technique.     

Comparative study of solubilities of hydrogen,nitrogen and carbon in α-iron

Solubility data of hydrogen, nitrogen and carbon in -iron are analysed on the basis of statistical thermodynamics. Present analysis appears to yield realistic values for the enthalpy term of the solutions of these interstitial elements into -Fe, while the entropy terms remain ambiguous. During the course of this analysis a parameter _x, which refers to the solubility limit of the specific interstitial element X (X=hydrogen, nitrogen or carbon), is also estimated; _H< _N< _C. This order of _X values appears to be in accord with the observation that, under normal conditions, the solubility of carbon is the highest and that of hydrogen the lowest in -Fe, while the atomic size increases with the order hydrogen相似文献   

The dielectric response of a commercial polybutylene terephthalate

Contour maps of complex relative permittivity within the range –170 to +175° C and 0.1 Hz to 3 MHz are presented for a commercial polybutylene terephthalate. The interdependence of and, as required by the Kramers-Krönig relations, is particularly apparent. Individual dispersion regions are attributed to- and-relaxation processes and to Maxwell-Wagner-Sillars polarizations. Possible explanations are proposed for the structure which is apparent in the-peak.     

Elastodynamic parameters for dynamic interface fracture mechanics

Summary Dynamic extension of cracks running along curvilinear interfaces of brittle bimaterials subjected to mechanical crack surface loads and superimposed thermal strains acting along the ligament is considered. This paper especially addresses the provision and discussion of elastodynamic interface parameters in order to assess quantitatively the bimaterial fracture in view of the governing physical features: applied mechanical and thermal strain loading, existence of an interface, crack-tip velocity and curvature of the interface contour. By utilizing the linear theory of thermoelasticity and adopting Stroh's method of generalized complex potentials, from the corresponding boundary and continuity conditions vectorial Hilbert problems are derived. It is shown that the parameters of the eigenvalues and of the eigenvectors of the Hilbert problems can be interpreted as elastodynamic interface mechanics parameters reading (,v _p, _Hf , _Hf ). Generalized Dundurs parameters of dynamics (, ) and consequently an associated generalized Dundurs diagram of dynamics are proposed. While the aforementioned elastodynamic interface parameters (, ,v _p, _Hf , _Hf ) do not assume the interface to be damaged, interfaces with running interface cracks generally cause two additional interface parameters, denoted as bimaterial constants (, _Hf ), where the latter is specific to the curvature of the interface in conjunction with the velocity of the interface crack. However, the bimaterial constants (, _Hf ) can be traced back to interface parameters for an uncracked bimaterial, namely to (, _Hf ).     

Coherent Brillouin Spectroscopy in Solid Parahydrogen

We applied coherent Brillouin spectroscopy to solid parahydrogen, and measured the Brillouin spectra of longitudinal acoustic modes at 5.6K. It was found that the linewidth of these spectra is 1.5MHz. From the observed Brillouin shift and the crystal orientation, the elastic stiffness was determined as C ₁₁=0.355±0.016GPa and C ₃₃=0.432±0.022GPa.     

The α- to β-Si3N4 transformation in the presence of liquid silicon

The compacts consisted of , -Si₃N₄ and free silicon are heat treated in the range 1650° C to 1750° C in an argon atmosphere in order to observe the following behaviours; the to phase transformation and variations of the microstructure during heat treatment in silicon nitride. For the microstructural observation of the heat treated specimens, the same grains in the polished surface were investigated before and after eliminating the retained silicon by etching. The to phase transformation, in this case, occurs via silicon melts irrespective of added -Si₃N₄. Both and phases are soluted and precipitated into molten silicon and their morphology are changed from an equiaxed shape to prismatic one. Although elongated grains are precipitated at low temperature or in the early stage of heat treatment, fine precipitated grains are mainly observed with increasing heat treating temperature.     

Varistor characteristics in PTCR-type (Ba,Sr)TiO3 ceramics prepared by single-step firing in air

This paper deals with donor, acceptor-codoped (Ba_0.4Sr_.6)TiO₃ ceramics with distinct varistor characteristics at room temperature, which were prepared by single-step firing in air. The materials, with the Curie point at around –90 °C, exhibited a large PTCR (positive temperature coefficient of resistivity) effect of more than seven orders of magnitude in the temperature range –90 °C (the resistivity 10³ · cm) to room temperature ( > 10¹⁰ · cm). An apparent dielectric constant of >20000 and tan < 0.05 (at 100 kHz) were observed for the present materials at room temperature, and moreover, the materials exhibited nonlinear current-voltage characteristics with the nonlinear coefficient, , in the range 7–12 and the varistor field, E_v, in the range 0.3–1.0 kV/cm. The value of in the present materials increased systematically with increasing in their PTCR temperature range. It has been found that there exists a close correlation between and the grain-boundary potential barrier height, e, obtained from the -T characteristic of the materials. An almost linear relationship was also found to exist between and log E_v for the present materials.     

Rheology of stimulated whole saliva in a typical pre-orthodontic sample population

The dynamic viscosity () of stimulated whole saliva in a typical pre-orthodontic sample population was characterized as a function of temperature (T). Samples were collected from 30 adolescents or young adults, after screening for factors that are known to have an effect on salivary viscosity. Using a cone and plate viscometer, 1.5 ml of stimulated whole saliva was evaluated at a constant shear rate of 450 s^-1 from T=20°C to T=40°C. Data from the -T plots showed a negative dependence of the form, =a–bT, over a range of from 1.08 to 2.45 centipoise (cps) at 34°C. Most of the samples fell into a narrow envelope, where the mean of the saliva samples ranged from 2.42±0.61 cps at 20°C to 1.57±0.32 cps at 37°C. With regard to sample stability, viscosity-time plots indicated that a small but predictable decrease in occurred during the 3 h period. The -T plots generated from fresh and frozen saliva samples demonstrated an appreciable change in as a result of refrigeration. With regard to sample reproducibility, viscometric data obtained from a typical pre-orthodontic patient over a 1-week period fluctuated within a fairly broad envelope of values.Presented, in part, at the 21st Annual Meeting and Exhibition of the A.A.D.R., Boston, Massachusetts, March, 1992.     

Experimental confirmation of the isotopic volume effect in superconducting molybdenum by means of energy-dispersive x-ray diffration at low temperatures

Differences in the lattice constants of Mo-100 and Mo-92 have been measured by x-ray diffraction, in order to search directly for the volume effect of isotopes in a superconductor. No significant difference in the lattice constanta(Mo-100)–a(Mo-92) could be detected at 290 K, while the differences –0.0014±0.0008 and –0.0029±0.0009 Å were detected at 85.3 and 4.31 K, respectively. These values, and their temperature dependence, are considered to be theoretically reasonable. The exponent in the isotope effect defined by T_cM^- is represented thermodynamically by =–( lnT _c / lnM)–( lnT _c / lnV)(d lnV/d lnM). From the results, d lnV/d lnM is found to be –0.033±0.009 at 4.31 K. Then, the second term representing the isotopic volume effect is estimated to be about 0.09, with lnT _c / lnV2.81. The observed value of is 0.33, so that the contribution of the second term, 0.09, is 27% of the value of . It becomes quite clear that the isotopic volume effect in superconducting Mo should not be neglected.     

Ageing characteristics of cast Zn-Al based alloy (ZnAl7Cu3)

Microstructure and ageing characteristics of a cast Zn-Al based alloy (ZnAl7Cu3) were studied using X-ray diffraction, electron scanning microscopy and back-scattered diffraction techniques. Two stages of phase transformation, i.e., decomposition of zinc rich phase and four phase transformation, + T + , were detected during ageing at 150°C. Electron back-scattered diffraction technique was applied in distinguishing both zinc rich and phases.     

Specific heat measurements of intercalation compounds M x TiS2 (M=3d transition metals) using ac calorimetry technique

Specific heats of 3d transition metal intercalates of 1T-CdI₂-type TiS₂, M _x TiS₂ (M=V, Cr, Mn, Fe, Co, and Ni; 0x1), have been measured in the temperature range 1.6–300 K using an ac calorimetry technique. The electronic specific heat coefficient (2–100 mJ/mole K²) and the Debye temperature _D (240–430 K) are found to depend on the guest 3d metals and their concentrations. All the intercalates show anomalous specific heat at low temperatures following an – lnT dependence ( and are constants), as found in dilute alloys.     

The specific heat of solid oxygen

Measurements have been made in the temperature range from 1.3° K to about 71°K with particular attention to the behavior at very low temperatures, and in the neighborhood of the - transition at about 23.89° K. Assuming that near 0° K each molecule moves as a single mass point with the passage of lattice waves, the effective Debye temperature at 0° K is extrapolated to be 104±2° K. As the temperature rises above 10° K, the specific heat rises more rapidly than a reasonable Debye model would predict, suggesting the appearance of additional degrees of freedom, which are thought to be the superposition of a librational motion of the molecules superposed on the longitudinal and transverse lattice waves controlling the motion of a molecule's center of mass. The specific heat shows a very sharp high spike at the - transition with an entropy change of aboutR ln 1.65; there is no evidence for a latent heat associated with this transition.