关于M－3Y力等效G矩阵元在重核区的有效性

采用Ｍ—３Ｙ力等效Ｇ矩阵元，并利用折线图多体方法计算了２１０Ｐｂ、２０６Ｐｂ以及２０６Ｈｇ和２１０Ｐｏ的低能谱．结果表明，Ｍ—３Ｙ力等效Ｇ矩阵元基本上适用于此核区的核结构微观计算．     

Modification of rubber surface by UV surface grafting

Rubber surface is subjected to ultraviolet radiation (UV) in the presence of allylamine and radiation sensitizer benzophenone (BP). Fourier transform infrared spectral studies reveal the presence of allylamine on the surface. The presence of irregular needle shapes on the surface as observed in scanning electron micrographs also confirms the polymerized allylamine on the surface. Allylamine coatings have been further confirmed from atomic force microscopy (AFM) analysis. Thermogravimetric analysis (TGA) reveals that allylamine coating on the rubber surface lowers the thermal degradation rate. The contact angle between the water and rubber surface decreases for the modified rubber surface confirming the surface modification due to UV surface grafting.     

Large- N Weinberg-Tomozawa interaction and spin-flavor symmetry

The construction of an extended version of the Weinberg-Tomozawa Lagrangian, in which baryons and mesons form spin-flavor multiplets, is reviewed and some of its properties discussed, for an arbitrary number of colors and flavors. The coefficient tables of spin-flavor irreducible representations related by crossing between the s-, t- and u-channels are explicitly constructed.     

Relationship between processing conditions, defects and thermal degradation of poly(vinylidene fluoride) in the β-phase

Poly(vinylidene fluoride), PVDF, in its β-phase is an electroactive polymer with many technological applications. There are two main ways to prepare this polymer in its electroactive β-phase: by high temperature stretching from the α-phase and directly from solution. In this paper, the influence of the processing methods in the thermal stability of the samples was studied by UV-VIS spectroscopy and thermogravimetric analysis. The number of chain defects was measured by ¹H NMR. The results obtained were compared to a commercial β-PVDF sample. The number of head to head defects in the different samples is found to be between 6% and 9%. The onset temperature for thermal degradation and the average activation energy (∼76.5 kJ mol⁻¹) of the process are approximately equal for the α-phase sample and the β-phase obtained from it. Larger values of the onset temperature and average activation energy (∼100 kJ mol⁻¹) are found for the β-phase sample directly obtained from the solution and for the commercial β-phase sample. The thermal degradation of the samples occurs in two steps, independently of the phase of the sample, the degree of crystallinity and the processing method.     

Electrical conductivity of 4-tricyanovinyl-N,N-diethylaniline

Physical characterizations of 4-tricyanovinyl-N,N-diethylaniline, TCVA, have been reported. The differential scanning calorimetry measurements of TCVA showed that this compound is stable up to 423 K. The temperature dependence of electrical conductivity, in the temperature range from 298 to 403 K, was studied on pellet samples of TCVA with evaporated ohmic Au electrodes. The electrical conductivity was found to be 7.01×10⁻⁹ Ω⁻¹ cm⁻¹ at room temperature. The temperature dependence of the electrical conductivity is typical for semiconducting compounds. The current density-voltage (J-V) characteristics of TCVA pellet samples have been investigated at different temperatures. In low-voltage region, the conduction current obeys Ohm's law while the charge transport phenomenon appears to be space-charge-limited current in the higher voltage regions.     

Thermal analysis of InP-based quantum cascade lasers for efficient heat dissipation

We have theoretically investigated the thermal characteristics of double-channel ridge–waveguide InGaAs/InAlAs/InP quantum cascade lasers (QCLs) using a two-dimensional heat dissipation model. The temperature distribution, heat flow, and thermal conductance (G _th) of QCLs were obtained through the thermal simulation. A thick electroplated Au around the laser ridges helps to improve the heat dissipation from devices, being good enough to substitute the buried heterostructure (BH) by InP regrowth for epilayer-up bonded lasers. The effects of the device geometry (i.e., ridge width and cavity length) on the G _th of QCLs were investigated. With 5 μm thick electroplated Au, the G _th is increased with the decrease of ridge width, indicating an improvement from G _th=177 W/K⋅cm² at W=40 μm to G _th=301 W/K⋅cm² at W=9 μm for 2 mm long lasers. For the 9 μm×2 mm epilayer-down bonded laser with 5 μm thick electroplated Au, the use of InP contact layer leads to a further improvement of 13% in G _th, and it was totally raised by 45% corresponding to 436 W/K⋅cm² compared to the epilayer-up bonded laser with InGaAs contact layer. It is found that the epilayer-down bonded 9 μm wide BH laser with InP contact layer leads to the highest G _th=449 W/K⋅cm². The theoretical results were also compared with available obtained experimentally data.     

Thermal and some physical properties of glasses in the La2O3−CaO−B2O3 ternary system

Glasses in the La₂O₃−CaO−B₂O₃ ternary system were studied. The glass forming range as determined by the appearance of the annealed cast was found to match previously published findings. Clear glasses were formed in the composition range of 5.7−19.1 mol% La₂O₃ with constant B₂O₃ content of 71.4 mol%, and in glasses of constant La₂O₃:CaO ratio of 1:4 with B₂O₃ content in the range of 71.4-55.0 mol%. The non-linear optical crystalline phase La₂Ca₂B₁₀O₁₉ was crystallized from the clear glasses after heat treatments, as determined by powder XRD. Two types of the LaBO₃ crystalline phases were detected in the partially and the fully crystallized glass compositions outside the glass forming range. Data are reported for the glass transition temperature (T_g), dilatometric softening point (T_d), linear coefficient of expansion (α), onset crystallization temperature (T_x), exothermal peak temperature (T_P), density (ρ) and index of refraction (n_D) in the clear glasses.     

Crystallization behavior of (GeS2)0.1(Sb2S3)0.9 glass

The crystal growth kinetics of antimony trisulfide in (GeS₂)_0.1(Sb₂S₃)_0.9 glass has been studied by microscopy and DSC. The linear crystal growth kinetics has been confirmed in the temperature range 492 ? T ? 515 K (E_G = 405 ± 7 kJ mol⁻¹). The applicability of standard growth models has been assessed. From the crystal growth rate corrected for viscosity plotted as a function of undercooling it has been found that the most probable mechanism is interface controlled 2D nucleated growth. The non-isothermal DSC data, corresponding to the bulk sample, can be described by the Johnson-Mehl-Avrami equation.     

Structure and thermomagnetic properties of powders produced from melt spun FeNbBCu ribbons

Amorphous ribbons of Fe₇₇Nb₇B₁₅Cu₁ prepared by melt-spinning and powders produced from them by ball-milling were characterized by means of calorimetry, X-ray diffraction, scanning electron microscopy and vibrating sample magnetometry. Upon thermal treatment the amorphous alloy experiences a primary crystallization that leads to bcc-Fe nanocrystals dispersed in an amorphous matrix. Magnetic measurements indicate that this alloy in the amorphous and nanocrystalline state is a good soft magnetic material. Values of saturation magnetization and coercivity are 120 Am²/kg and 5 A/m respectively, for the alloy in the nanocrystalline state. Pre-annealing, post-relaxation and nanocrystallization as well as various milling parameters were explored and the structural and magnetic changes induced have been studied. The analysis of the particle size distribution and morphology of the powders show that the brittleness resulting from pre-annealing of the ribbons is very effective in reducing the particle’s size. Recovery of the high coercitive field induced by milling is achieved by post-annealing to an extent that depends mostly on the milling conditions.     

A simple thermal decomposition synthesis, magnetic properties, and cytotoxicity of La0.7Sr0.3MnO3 nanoparticles

This study reports the new and simple synthesis of magnetic La_0.7Sr_0.3MnO₃ (LSMO) nanoparticles by thermal decomposition method using acetate salts of La, Sr and Mn as starting materials. To obtain the LSMO nanoparticles, thermal decomposition of the precursor is carried out at the temperatures of 600, 700, 800, 900, and 1000°C for 6 hours. The synthesized LSMO nanoparticles were characterized by XRD, FT-IR, TEM and SEM. Structural characterization shows that the prepared particles consisted of two phases of LaMnO₃ (LMO) and LSMO with crystallite sizes ranging from 18 to 55 nm. All the prepared samples have a perovskite structure which changes from cubic to rhombohedral with the increase in the thermal decomposition temperature. Basic magnetic characteristics such as saturation magnetization (M _S) and coercive field (H _C) are evaluated by sample vibrating magnetometry at room temperature (20°C). The samples show soft ferromagnetic behavior with M _S values of ∼9–55 emu/g and H _C values of ∼8–37 Oe, depending on the crystallite size and thermal decomposition temperature. The relationship between the crystallite size and the magnetic properties is presented and discussed. The cytotoxicity of synthesized LSMO nanoparticles was also evaluated with NIH 3T3 cells and the result showed that the synthesized nanoparticles were not toxic to the cells as determined from cell viability in response to the liquid extraction of LSMO nanoparticles.