Thermal conductivity of nitrogen in the temperature range 350–2500 K

The thermal conductivity of nitrogen is determined in a conductivity column instrument in the temperature range of 338 to 2518 K with an estimated uncertainty of about ± 1·5 per cent. The experimental data points are correlated by a cubic polynomial in temperature, viz. k(T)/(mW m^-1 K^-1) = 12·18 + 0·05224(T/K) - 0·6482 × 10^-6(T/K)² - 0·2765 × 10^-9(T/K)³. These conductivity values determined from heat transfer data taken in the continuum regime are found to be in fair agreement with the values obtained from similar data referring to low pressure range.

The present results are compared with the conductivity determinations of other workers and with the predictions of various theories developed for polyatomic gases. It is pointed out that a reliable calculation of thermal conductivity over an extended temperature range is impossible at the present time due to the absence of a large variety of experimental molecular data needed for such an effort. Average values of the vibrational energy diffusion coefficient, D _vib, are computed from the present k(T) data.     

Thermal conductivity of the single-crystal monoisotopic 29Si in the temperature range 2.4–410 K

Physics of the Solid State - The temperature dependence of the thermal conductivity κ(T) of single-crystal silicon highly enriched in 29Si (99.919%) isotope has been measured in the...     

Thermal conductivity and thermal diffusivity of samarium in the temperature range of 293–1773 K

The thermal conductivity and the thermal diffusivity coefficients of samarium have been measured by the laser flash method in the temperature interval of 293–1773 K in solid and liquid states including the regions of phase transitions. The measurement errors of the heat transfer coefficients were ±(3–6)%. The approximation equations and the tables of reference data for the temperature dependence of properties have been obtained. The obtained results have been compared with the available literature data.     

Stress characteristics of creep of alpha-Zr in the temperature interval 300–900 K

The stress experiments of alpha-Zr were performed within the temperature interval 300 to 900 K using the incremental loading method. The temperature interval may be divided into three regions — the low temperature region (300–475 K), the transient region (475–775 K) and the high temperature region (above 775 K). The transient region was characterized by the maximum of the strain-rate sensitivity parameterm and also the creep deformation was — to a certain degree — affected by the athermal mechanism.The authors would like to thank Professor J.adek, DrSc, for many valuable discussions, unfailing support and continual encouragement.     

Thermal conductivity of single-crystal ZrO2-Y2O3 solid solutions in the temperature range 50–300 K

The thermal conductivity of ZrO_2−x Y₂O₃ single crystals (x = 0.5, 1.5, 2.0, 2.5, 3.0, 8.0 mol %) has been studied experimentally in the temperature range 50–300 K. The influence of high-temperature annealings on the thermal conductivity has been analyzed.     

Thermal conductivity of large-grain niobium and its effect on trapped vortices in the temperature range 1.8–5 K

Experimental investigation of the thermal conductivity of large grain and its dependence on the trapped vortices in parallel magnetic field with respect to the temperature gradient \(\nabla T\) was carried out on four large-grain niobium samples from four different ingots. The zero-field thermal conductivity measurements are in good agreement with the measurements based on the theory of Bardeen–Rickayzen–Tewordt (BRT). The change in thermal conductivity with trapped vortices is analysed with the field dependence of the conductivity results of Vinen et al for low inductions and low-temperature situation. Finally, the dependence of thermal conductivity on the applied magnetic field in the vicinity of the upper critical field H _c2 is fitted with the theory of pure type-II superconductor of Houghton and Maki. Initial remnant magnetization in the sample shows a departure from the Houghton–Maki curve whereas the sample with zero trapped flux qualitatively agrees with the theory. A qualitative discussion is presented explaining the reason for such deviation from the theory. It has also been observed that if the sample with the trapped vortices is cycled through T _c, the subsequent measurement of the thermal conductivity coincides with the zero trapped flux results.     

Thermal Hall conductivity with sign change in the Heisenberg–Kitaev kagome magnet

The Heisenberg-Kitaev(HK) model on various lattices has attracted a lot of attention because it may lead to exotic states such as quantum spin liquid and topological orders.The rare-earth-based kagome lattice(KL) compounds Mg₂RE₃Sb₃O₁₄(RE=Gd,Er) and(RE=Nd) have q=0,120° order and canted ferromagnetic(CFM) order,respectively.Interestingly,the HK model on the KL has the same ground state long-range orders.In the theoretical phase diagram,the CFM phase re...     

Phase diagram of the Al–Er–Mo ternary system at 873 K

The phase relationship in the Al–Er–Mo ternary system at 873 K has been investigated based on the equilibrated method mainly by means of X-ray powder diffraction and scanning electron microscopy. The existence of 10 binary compounds and two ternary compounds has been confirmed. The results present that the isothermal section at 873 K is governed by 15 single-phase regions, 29 two-phase regions and 15 three-phase regions. By using the phase-disappearing method, Al₈Mo₃ has a narrow homogeneity range (from 72 to 73 at% Al), while the homogeneity range of AlMo₃ is from 21% to 28.5% at% Al. Also, the maximum solubility of Al in Mo is about 16 at%.     

Heat transfer coefficients of liquid indium in the temperature range 470–1275 K

Thermal conductivity and thermal diffusivity coefficients of liquid indium have been determined in the range of temperatures from 470 to 1275 K by the laser flash method. Errors of heat transfer coefficients are ±(3.5–5) %. Approximating equations and tables of reference data have been developed for temperature dependence of properties. Measurement results have been compared with the data available in the literature. Temperature dependence of Lorentz number has been calculated up to 1000 K.     

The isothermal section of the Tb–Co–Cr ternary system at 873 K

The isothermal section of the phase diagram of the Tb–Co–Cr ternary system at 873?K was investigated by means of X-ray diffraction, metallography, and scanning electron microscopy equipped with energy dispersive X-ray spectroscopy. Ternary phases and their lattice parameters as a function of composition of solid solution were systematically studied. The existence of one ternary phase reported previously was confirmed. The ternary compound Tb(Co,?Cr)₁₂ crystallizes with ThMn₁₂-type structure, space group I4/mmm. The linear homogeneity range along the line of 7.69 at.% Tb in TbCo_{12? x} Cr _x was found to be about x?=?3.6–5.7, i.e., 27.7–43.8 at.% Cr. The lattice parameters are a?=?0.8326–0.8352?nm and c?=?0.4709–0.4740?nm. The maximum solid solubilities of Cr in Tb₂Co₁₇, TbCo₃, and TbCo₂ are about 20.0, 8.2, and 7.9 at.%, respectively.     

Cross sections of in the centre-of-mass energy interval 1850–2160 MeVin the centre-of-mass energy interval 1850–2160 MeV

Cross-sections for are reported in the centre-of-mass energy interval 1850–2160 MeV. The data come from a deuterium bubble chamber experiment atK ⁻ beam momenta of 1.45 and 1.65 GeV/c. Taking into account the Fermi motion of the neutron in the deuteron, this momentum range corresponds to the centre-of-mass energy interval of 1850–2160 MeV.     

Phase separation in Na–K liquid alloy

The quasi-chemical expression for weakly interacting binary alloy has been applied to obtain energy parameters and their temperature derivatives for Na–K liquid alloy at 384?K. These energy parameters have then been used to calculate thermodynamic functions, such as free energy of mixing, heat of mixing, entropy of mixing and microscopic functions, such as concentration fluctuation in long wavelength limit, Warren–Cowley short-range order parameter, ratio of mutual and self-diffusion coefficients. The analysis reveals that the energy parameters are temperature dependent and the Na–K liquid alloy at 384?K is a weakly interacting homocoordination system. The observed thermodynamic properties of Na–K alloy in molten state have successfully been explained by assuming Na₂K complex on the basis of the quasi-chemical formalism for a weakly interacting system.     

Measurement of the space–time interval in modified gravity theories in Palatini formalism

There are strong motivations that lead cosmologists to consider alternatives to Einstein’s theory of gravity in Palatini formalism. In addition, there are two distinguishable local frames in this formalism in which one of them is local inertial frame and the equivalence principle is satisfied. Different features of speed of light such as the causal structure constant, electromagnetic and gravitational wave velocities and Einstein velocity will not coincide in this local inertial frame for extended gravity theories in Palatini formalism. On the other hand, both the measurement of time and exchange of a signal between the distant points are required to determine spatial distances. In a particular situation where these aspects of the speed of light do not coincide, the distance determination will become more demanding because light will follow a time-like geodesic of the metric. In modified gravity theories in Palatini approach, theories involve a varying speed of photon. Therefore these kinds of theories must be based on some other technique of measuring spatial distances than radar or some terms should be corrected in the line element in the proposed model. We found out we should consider a coefficient which is proportional to energy density in each era, in the line element in order to be able to use radar for measuring distance in modified gravity theories in Palatini formalism. Analysis of some observational data will be affected by considering this coefficient in the line element.     

Thermal Conductivity of poly-p-phenylene-2,6-benzobisoxazole Film along the In-Plane Axis in the 10–300 K Temperature Range

The thermal conductivities of compression molded thin films of poly-p-phenylene-2,6-benzobisoxazole (PBO) were measured in directions along an in-plane axis in the 10–300?K temperature range by a steady-state heat flow method, with interest in the use of the material for superconductivity applications. The thermal conductivities of the PBO films increased from 0.3?W/mK to 9.0?W/mK with increasing temperature from 10?K to 300?K and these were much higher than those of polyimide films, epoxy resin and glass fiber reinforced plastics at all temperatures. The 9.0?W/mK at 300?K was 60% of that of stainless steel (SUS304). It was 6?W/mK at 150?K, which was half that of SUS304 and was 3.3?W/mK at 77?K, which was 33% of that of SUS304. The thermal conductivities of the PBO films were lower than those of a cloth of high strength ultrahigh molecular weight polyethylene fiber reinforced plastics in the 30?K–180?K temperature range and were almost equivalent to its values in the 180?K–300?K temperature range. The main contribution to the thermal conduction in the PBO films was from thermal phonon conduction along the molecular chains. Although many kinds of high thermal conductivity polymeric materials have been prepared by a uni-directional drawing process or by adding high thermal conductive additives, the PBO film showed high thermal conductivity without a uni-directional drawing process or high thermal conductive additive.     

Thermal conductivity of Pb-Mg-Zr alloys and the thermal resistance of the interface between alloys and EP-823 steel in the temperature range of 300–900°C

A technique for measuring the thermal resistance of the liquid metal–structural steel interface is proposed. The results ofmeasurements of the thermal resistance of the interface between Pb-Mg-Zr alloys and EP-823 steel and the thermal conductivity of Pb-Mg-Zr alloys in the temperature range of 350–900 °C are presented.     

Isotopic effect in the solid–liquid phase diagram of quantum clusters

Applying the Fourier path integral formalism to the isothermal-isobaric ensemble, the solid–liquid transition for 13-atom pure Lennard–Jones clusters was characterized. The masses of the clusters were taken as the masses of hydrogen, deuterium and tritium, hence isotopic effects of quantum clusters were considered. The parallel tempering Monte Carlo algorithm was used to solve all multidimensional integral in the FPI method. The volume of the system was defined with respect to the centroids of the quantum particles and a variable constraining potential was used to restrict undesirable thermodynamic events. The maximum value of the constant pressure heat capacity at a given temperature was used to identify the melting temperature. Pressure versus temperature phase diagrams were constructed for these systems with and without the inclusion of quantum effects. A significant difference in the melting temperature was encountered for the different isotopes due to quantum contribution.     

Temperature range of the liquid–glass transition

It has been shown that the currently used method for calculating the temperature range of δT_g in the glass transition equation qτ_g = δT_g as the difference δT_g = (T₁₂–T₁₃) results in overestimated values, which is explained by the assumption of a constant activation energy of glass transition in deriving the calculation equation (T₁₂ and T₁₃ are the temperatures corresponding to the logarithmic viscosity values of logη = 12 and logη = 13). The methods for the evaluation of δT_g using the Williams–Landel–Ferry equation and the model of delocalized atoms are considered, the results of which are in satisfactory agreement with the product qτ_g (q is the cooling rate of the melt and τ_g is the structural relaxation time at the glass transition temperature). The calculation of τ_g for inorganic glasses and amorphous organic polymers is proposed.