Temperature dependence of electrical resistivity of deformed and undeformed V-rich V3Si single crystals

The electrical resistivity (T) of V-rich V₃Si single crystals (T _c-11.4 K) was measured from 4.2 to 300 K along the directions of [1 0 0] and [1 1 1] before and after plastic deformation at 1573 K. Anisotropy of (T) was observed although V₃Si has the cubic A15 structure. Plastic deformation does not affect the normal-state (T) behaviour but changes the normal-superconducting transition width T_c. At low temperatures (T _c<T 40 K), (T) varies approximately as T ⁿ where n-2.5 and this behaviour does not contradict the (0)- phase-diagram plot proposed by Gurvitch, where is the electron-phonon coupling constant and (0) is the residual resistivity.     

Solidification behavior of Al-Si-Fe alloys and phase transformation of metastable intermetallic compound by heat treatment

Solidification behavior of Al-20 wt% Si-8 wt% Fe and Al-30 wt% Si-5 wt% Fe alloys during cooling with a cooling rate of 10 K/min has been studied using optical microscopy, X-ray diffractometry, differential thermal analysis, scanning electron microscopy and energy dispersive X-ray spectroscopy. In Al-20Si-8Fe alloy, metastable -Al₄FeSi₂ phase with tetragonal structure formed first from melt, followed by primary Si precipitation and then remaining liquid solidified finally into ternary eutectic of -Al, Si and phases. However, in Al-30Si-5Fe alloy, primary Si formed first, followed by the phase precipitation and then eutectic solidification. During isothermal heat treatment of as-solidified alloys, phase transformation from the phase to equilibrium phase began at the interface between phase and -Al matrix and progressed toward the inside of phase with co-precipitation of Si particles due to the difference in composition between -Al₄FeSi₂ and -Al₅FeSi phases.     

Standard Gibbs' energies of formation of BaCuO2, Y2Cu2O5 and Y2BaCuO5

The Gibbs' energies of formation of BaCuO₂, Y₂Cu₂O₅ and Y₂BaCuO₅ from component oxides have been measured using solid state galvanic cells incorporating CaF₂ as the solid electrolyte under pure oxygen at a pressure of 1.01×10⁵ Pa BaO + CuO BaCuO₂ G _f,ox ^o (± 0.3) (kJ mol^–1)=–63.4–0.0525T(K) Y₂O₃ + 2CuO Y₂Cu₂O₂ G _f,ox ^o (± 0.3) (kJ mol^–1)=18.47–0.0219T(K) Y₂O₃ + BaO + CuO Y₂BaCuO₅ G _f,ox ^o (± 0.7) (kJ mol^–1)=–72.5–0.0793T(K) Because the superconducting compound YBa₂Cu₃O_7– coexists with any two of the phases CuO, BaCuO₂ and Y₂BaCuO₅, the data on BaCuO₂ and Y₂BaCuO₅ obtained in this study provide the basis for the evaluation of the Gibbs' energy of formation of the 1-2-3 compound at high temperatures.     

The effect of silica characterization on the microstructure of BaFe12O19 ferrites

The anisotropically formed BaFe₁₂O₁₉ ferrites were prepared from the hot-rolled mill scale and silica was added to the ferrite during fine milling in the range 0.15 to 0.50 wt%. These ferrites were sintered at 1220° C for 2 h. The grain growth of the ferrites is dominantly influenced by the sizes of the silica added. Coarse-grain ( 1m) silica tends to promote discontinuous grain growth, which increases drastically with slightly increasing amounts of silica added, while fine-grain ( 0.013m) silica tends to retain fine grain microstructures with the same increasing amount of silica. The average grain size of the ferrite without silica addition was 8 to 10m. The size was increased to as large as 30m on addition of 0.15% coarse-grain silica and the microstructure was full of extremely large grains on the addition of 0.50% coarse-grain silica.     

Effects of Y2O3 and La2O3 addition on the crystallization of Li2O·Al2O3·4SiO2 glass-ceramic

Effects of adding Y₂O₃ and La₂O₃ on the crystallization of -quartz solid solution (ss) and the subsequent -quartz ss to -spodumene transformation of Li₂O·Al₂O₃·4SiO₂ glass-ceramic were investigated. Adding 4 mol% YO_3/2 or 8 mol % LaO_3/2 effectively improved the control of the crystallization process of the glass. Y₂O₃ did not effectively induce bulk crystallization of -quartz ss, but can reduce the rate of surface crystallization. La₂O₃ completely suppressed the surface crystallization and promoted a uniform, bulk crystallization of -quartz ss. For both the Y₂O₃- and La₂O₃-doped glasses, the kinetics for glass crystallization to -quartz ss was delayed as the doping level increased. Except for the 8 mol % LaO_3/2-doped glass in which no -spodumene was formed, the kinetics for the -quartz ss to -spodumene transformation for the doped glasses was enhanced compared with that for the undoped glass. For the 4 and 8 mol % YO_3/2-doped compositions, the relative amount of -spodumene to -quartz revealed an anomalous decrease trend with heating temperature in a particular temperature range. This can be explained by the surface crystallization characteristic, which induced an overlap of crystallization and -quartz ss to -spodumene transformation. Glass doped with 8 mol % LaO_3/2 exhibited an Avrami exponent of about 2.4 and an activation energy for crystal growth of -quartz ss of about 418 kJ mol^–1.     

Internally Consistent Thermodynamic Description of Three-Component Liquid-Metal Systems at High Temperatures in the Entire Region of Concentration Triangle

A method is suggested for the investigation of the thermodynamic properties of ternary liquid-metal alloys at high temperatures in the entire region of concentration triangle. The method is demonstrated for a Na–K–Cs ternary system. Data are obtained for the enthalpy and Gibbs energy of formation of alloy in the temperature range of 200 T 1200 K and concentration range of 0 x _{i (j, k)} 1. The results reveal a very fine effect associated with the temperature rise, namely, the inversion of excess partial Gibbs energy G¯ _i ^*= RTln _i ( _i is the activity coefficient of the liquid component) and the change of sign of deviation of partial pressure, as well as of total pressure, from the respective values in accordance with Raoult's law. The obtained results may be used to interpret the available literature data on independent measurements of the saturation pressure.     

Synthesis and characterization of silicon nitride whiskers

Silicon nitride whiskers were synthesized by the carbothermal reduction of silica under nitrogen gas flow. The formation of silicon nitride whiskers occurs through a gas-phase reaction, 3SiO(g)+3CO(g)+2N₂(g)=Si₃N₄()+3CO₂(g), and the VS mechanism. The generation of SiO gas was enhanced by the application of a halide bath. Various nitrogen flow rates resulted in different whisker yields and morphologies. A suitable gas composition range of N₂, SiO and O₂ is necessary to make silicon nitride stable and grow in a whisker form. The oxygen partial pressure of the gas phase was measured by an oxygen sensor and the gas phase was analysed for CO/CO₂ by gas chromatography. Silicon nitride was first formed as a granule, typically a polycrystalline, and then grown as a single crystal whisker from the {1 0 0} plane of the granule along the 210 direction. The whiskers were identified as-sialon with Z value ranging from 0.8 to 1.1, determined by lattice parameter measurements.     

Properties of Va metal-B films prepared by r.f.-sputtering

Ta_100-x B _x alloy films were prepared by r.f.-sputtering in the chemical composition range 45 x 77. Ta_100-x B _x (45 x 58) films consist of the amorphous phase, while the TaB₂ crystal phase was observed in Ta_100-x B _x (66 x 77) films. A remarkable preferred orientation with the (001) plane of TaB₂ parallel to the film surface was observed in Ta₃₄B₆₆. The d.c. electrical conductivity of Ta_100-x B _x (45 x 77) films decreases with increasing boron content in the range 6.7 × 10³ to 1.3 × 10^3–1 cm^–1. The micro-Vickers hardness of Ta_100-x B _x (45 x 77) films was in the range 2200 to 2600 kg mm^–2.     

Magnetic properties of highly dilutedPdFex andPtFex-alloys. Part II. Susceptibility at micro- and milli-kelvin temperatures

We have measured the 16 Hz susceptibility of the giant magnetic moments induced by Fe impurities in highly dilutedPdFe_x andPtFe_x samples with 2.5 ppm x 75 ppm in a wide temperature range, 30 K T 300 mK, and at static magnetic fields 0,01 mT B 25 mT. We find spin glass freezing at Tf(X)/X0,19mK/ppm Fe forPdFe_x and the larger value 0.26 mK/ppm Fe forPtFe_x. This is the first observation of spin glass freezing inPtFe_x. In the low-temperature range T 0.5T_f(x), the susceptibilities follow — ₀ T with small zero-temperature ₀ values forPdFe_X and vanishing ₀ values forPtFe_x. In the paramagnetic high-temperature range, we find (T — )^it-1 at T 10 mK independent of x forPdFe_x, and at T 2Tf(x) dependent of x forPtFe_x with vanishing values for both systems. The data compare well to the predictions of the Thouless-Anderson-Palmer TAP approach of the Sherrington-Kirkpatrick SK model for spin glasses.     

Microstructural study of two LAS-type glass-ceramics and their parent glass

The two glass-ceramics studied here derive from the complex system (MgO,ZnO,Li₂O)-Al₂O₃-SiO₂ and are obtained by controlled devitrification of the same parent glass. Although they have the same chemical composition, one is a -quartz (or -eucryptite) type while the other one is a -spodumene glass-ceramic. A detailed microstructural analysis of these materials has been performed at different scales by several complementary characterization methods (SEM, TEM, DTA, XRD and FTIR). This extensive study has shown the great microstructure difference (grain distribution, grain size, nature of vitreous and crystalline phases) between these two glass-ceramics obtained from the same parent glass.     

Die Herleitung von Schalengleichungen über ein erweitertes Variationsprinzip bei Berücksichtigung der Querschubverzerrungen

Ohne ZusammenfassungBezeichnungen L Bezugsgrößen für dimensionslose Koordinaten - L charakteristische Schalenabmessung - t Schalendicke - Schalenparameter - körperfeste, krummlinige, dimensionslose Koordinaten der Schalenmittelfläche - Dimensionslose Koordinate in Richtung der Schalennormalen - i, j,...=1,2,3 Indizierung des dreidimensionalen Euklidischen Raumes - ,,...=1,2 Indizierung des zweidimensionalen Riemannschen Raumes - (...), Partielle Differentiation nach der Koordinate - (...), Kovariante Differentiation für Tensorkomponenten des zweidimensionalen Raumes nach der Koordinate - (...)| Kovariante Differentiation für Tensorkomponenten des dreidimensionalen Raumes nach der Koordinate - Variationssymbol - a ,a ₃ Basisvektoren der Schalenmittelfläche - V Verschiebungsvektor - U ,U ₃ Verschiebungskomponenten des Schalenraumes - v ,w,w ,W Verschiebungskomponenten der Schalenmittelfläche - Verhältnis der Metriktensoren des Schalenraumes und der Schalenmittelfläche - _ik Verzerrungstensor des Raumes - _{(, )}, Symmetrische Verzerrungstensoren der Schalenmittelfläche - _{[, ]} Antimetrischer Term des Verzerrungsmaßes - ^, Spannungstensor - n ,m ,q Tensorkomponenten der Schnittgrößenvektoren - p ,p,c Tensorielle Lastkomponenten     

Precipitation of β particles in a fully lamellar Ti-47Al-2Nb-1Mn-0.5W-0.5Mo-0.2Si (at.%) alloy

The precipitation of (B2) particles at intermediate temperatures, between 760°C and 1050°C, is investigated in a fully lamellar TiAl-WMoSi alloy. The particles, having a thin-plate shape, usually precipitate on the ₂ side of ₂/ interfaces at low aging temperatures in an uneven two-dimensional growth mode. While those formed at higher aging temperatures, growing extensively within the ₂ plate and into the adjacent lamellae, have an ellipsoid shape. The growth of particles at low aging temperatures yields an activation energy of about 366 kJ/mol. It is suggested that at low aging temperatures the growth of particles proceeds via an ₂ precipitation process controlled by diffusion of W and Mo along the /₂ and / interfaces.     

Submillimeter surface impedance and relaxation: A case study of quasi-two-dimensional YBa2Cu3Ox

Surface impedance measurements in the normal and superconducting state are an excellent method to study the conduction electron dynamics in metals. This holds especially in the relaxation range, i.e., for distances traveled in one r.f. periods= _F/(_f is the Fermi velocity) being smaller or of the order of the penetration depth and mean free pathl. For materials with _F<-10⁷ cm/sec the relaxation range is easily accessible forf>0.1 THz. Then, in the normal state, relaxation defines the surface impedance with a penetration depth approaching the London penetration depth _L, andR _0l/2 as surface resistance allowing a measure of _L and relaxation time (T, ). In the superconducting state the photon interaction scales with _F/_L=l/ ( _f is the dimension of Cooper pairs for l) and causes at low frequencies an absorption rate growing with, which is decreasing with _F/l. The rate increase proportional to turns to a decrease above 0.1 THz, being accompanied by a decrease of with frequency which is stronger for large and small _F/l. These characteristic dependences allow a measurement of material parameters, anisotropy, and dynamics of electrons. To evaluate the consequences of theâ, b, and-direction anisotropy, the integral kernels for normal and superconducting surface impedances in its nonintegrated, angle-dependent form are presented, analyzed, and compared with impedance measurements above 0.1 THz of YBa₂Cu₃O_x.     

Solid state phase transformation of BaB2O4 during the isothermal annealing process

Solid-state phase transformation of BaB₂O₄ during the isothermal annealing process for both to and to were investigated using a platinum crucible. For the -phase crystal at the -phase stable temperature (> 925 °C), the phase transforms to the phase perfectly below the melting temperature of 1100 °C. Meanwhile, for the -phase crystal at the -phase stable temperature (< 925 °C), the phase transforms to the phase perfectly above 800 °C. There is some difference in phase transformation behaviour between bulk-shape crystals and the powder, caused by thermal stress.     

Application of inert radioactive gases in the study of solids

The behaviour of different iron salts (FeSO₄.7 H₂O, FeC₂O₄.2 H₂O, Mohr's salt, and basic iron carbonate) was studied by means of the emanation method, DTA and dilatometry. The salts were heated within the temperature range of 20 to 1100 C, under identical conditions. The results obtained are compared and the process of thermal decomposition of the different salts is discussed.The activity of ferric oxide obtained by decomposition of various iron salts is estimated, and it is suggested that the low activity of the sulphate-derived ferric oxides is related to a low thermal annealing rate, while the higher activities of the other two resultant ferric oxides are similarly related to higher thermal annealing rates.     

Zero-point motion and superfluid helium

We propose that He II exhibits macroscopic [ _P /N O(1)] quantum zero-point motion in momentum space, i.e., that a nonzero root-mean-square superfluid velocity exists even in an equilibrium superfluid system at rest. At absolute zero, using coherent states, we relate the uncertainty _P /N in the total momentumP (per particle) to the long-range-order (LRO) part of the phase gradient correlation function, which is proposed as an order parameter. The local equilibrium equation for the superfluid velocity potential derived by Biswas and Rama Rao yields, in the strict equilibrium limit, the equation determining this order parameter in terms of fluctuation correlations that remain to be determined. The order parameter is interaction dependent, nonzero atT=0 if (0)–₀V₀>0, and can vanish at some transition temperatureT when fluctuation terms become comparable to theT=0 value. (HereV _{0 0}, and (0) are the uniform parts of the potential, density, and chemical potential with shifted zero of energy, respectively.) A characteristic length (T), diverging atT=T , appears naturally, with its defining relation reducing to a macroscopic uncertainty relation ( _P /N)(0)=/2 atT=0. With certain assumptions it is shown that atT=0, LRO in the phase gradient correlation function is incompatible with off-diagonal long-range order (ODLRO) in the (r)(r) correlation function, and with nonzero condensate function.     

The mechanism of continuous dissolution of the lamellar structure in aged Al 22 at% Zn alloy

The mechanism of continuous dissolution was studied using transmission electron microscopy, X-ray diffraction and hardness measurements. The metastable phase was identified in the first stage of dissolution nucleating at the - boundaries. Interface dislocations at the - boundaries forming a perpendicular net in the 110 directions were identified as of screw character and of Burgers vector b=1/2a 110. During dissolution a change of shape of precipitates occurs leading to their fragmentation and to a change of the direction of boundaries into 110 directions.     

Thermal transport properties in helium near the superfluid transition. I.4He in the normal phase

The thermal conductivity and the associated relaxation time to reach steady-state conditions are reported for the normal phase of several very dilute mixtures of³He in⁴He (X<4 × 10^–6) at saturated vapor pressure near T. The measurements were made over the reduced temperature range 2.5 × 10^–6<<2×10^–1, where (T–T)/T, and are representative for pure⁴He. The spacing between the cell plates was 0.147 cm. The systematic uncertainty in the conductivity data is estimated to increase from 2% for =0.2 to 4% for =3 × 10^–6. The random scatter due to finite temperature resolution increases to 7% at the smallest . The data are in agreement within the combined uncertainty with recent ones by Tam and Ahlers (cell F, spacing 0.20 cm) and with previous ones in this laboratory taken with a different plate spacing. The thermal diffusivity coefficientD _T = / C _p obtained from is found to agree within better than 15% with the calculated one using data for , the density , and the specific heatC _p . Measurements of the effective boundary resistivityR _b in the superfluid phase are described.R _b is found to depend on the thermal history of the cell when cycled up to 77 K and above. Also,R _b shows the beginning of an anomalous increase for ¦¦10^–4. The possible reasons for this anomaly are discussed, and their impact on the analysis of conductivity data in the normal phase is appraised.     

Diffraction studies of β″-magnesium sialon

The compositions of high magnesium content -magnesium sialon crystals within the 3M/4X plane of the Mg-Si-Al-O-N system indicate some form of metal atom ordering wihtin the structure. Although it is not possible using X-ray diffraction to detect weak additional reflections arising from the ordering between magnesium, aluminium, and silicon atoms, such weak reflections are revealed on electron diffraction photographs for a phase, resulting in a tripling of the hexagonal latticec-dimension. These show to have a structure very similar to rhombohedral willemite (Zn₂SiO₄), with the (Mg, Al) metal atoms ordered with respect to the silicon atoms in a 21 ratio. However, there are some additional weak diffraction spots with indices not obeying the rhombohedral condition of –h+k+l=3n. It is proposed that the structure of this is identical to that of willemite and the extra spots are a result of some form of twinning, which implies the existence of ordered microdomains.