替代物热物性研究现状

1996年9月16—19日,我参加了在法国里昂INSA(Institut National de Sciences Ap-pliqtlees de Lyon)举行的第14届欧洲热物性会议。1 会议概况欧洲热物性会议始于1968年。1990年前每两年举行一次;1990年后,为配合全球范围三大洲热物性会议的均衡召开,改为每3年召开一次,即在美洲、欧洲与亚洲轮流举行,成为全球三大热物性会议之一。1993年8月在葡萄牙举行了第13届欧洲热物性会议。今年(1996年)9月在里昂召开了第14届欧洲热物性会议。

Design and Simulation of High-power LED Array Packaging

Thermal management is one of the key technologies for high-power Light emitting diode(LED)entering into the general illuminating field.Successful thermal management depends on optimal packaging structure and selected packaging materials.In this paper,the aluminum is employed as a substrate of LED,3×3 array chips are placed on the substrate,heat dissipation performance is simulated using finite element analysis(FEA)software,analyzed are the influences on the temperature of the chip with different convection coefficient,and optical properties are simulated using optical analysis software.The results show that the packaging structure can not only effectually improve the thermal performance of high-power LED array but also increase the light extraction efficiency.

Optical Properties of CdS.Nanobelts and Nanosaws Synthesized by Thermal Evaporation Method

By a simple one-step H2-assisted thermal evaporation method, high quality CdS nanos- tructures have been successfully fabricated on Au coated Si substrates in large scale. The as-synthesized CdS nanostructures consisted of sword-like nanobelts and toothed nanosaws with a single-crystal hexagonal wurtzite structure. The deposition temperature played an important role in determining the size and morphology of the CdS nanostruetures. A combination of vapor-liquid-solid and vapor-solid growth mechanisms were proposed to interpret the formation of CdS nanostructures. Photoluminescence measurement indicated that the nanobelts and nanosaws have a prominent green emission at about 512 nm, which is the band-to-band emission of CdS. The waveguide characteristics of both types of CdS nanos-truetures were observed and discussed.

Microscopic Theoretical Calculations of R—Line Thermal Shifts and Broadenings of MgO：Cr^3＋

By taking into account all the irreducible representations and their components in the electron-phonon interaction (EPI) as well as all the levels and the admixtures of basic wavefunctions within d3 electronic configuration, the values of all the parameters in the expressions of thermal shift (TS) and thermal broadening (TB) due to EPI for the ground level, R level and R line of MgO:Cr3+ have microscopically been evaluated; and then, TS and TB of R line and various contributions to them have uniformly been calculated. The results are in very good agreement with the experimental data. It is found that all the three terms of TS due to EPI are red shifts; the Raman term is the largest one, and the optical-branch term and neighbor-level term are important for TS; the contribution to TS from thermal expansion is blue shift, which is also important. The R-line TS of MgO:Cr3+ comes from the first-order term of EPI. The elastic Raman scattering of acoustic phonons plays a dominant role in R-line TB of MgO:Cr3+. For both TS and TB, it is very important to take into account all the admixtures of basic wavefunctions within d3 electronic configuration.

Substituent Effect on Infrared Spectra and Thermodynamic Properties of Polynitroamino Substituted Cyclopentane and Cyclohexane

Density functional theory method was employed to study the effect of the nitroamino group as a substituent in cyclopentane and cyclohexane, which usually construct polycyclic or caged nitramines. Based on the optimized molecular structures of two groups of monocyclic nitramines at the B3LYP/6-31G^＊＊ level, the infrared （IR） spectra were obtained and assigned by harmonic vibrational analysis. The calculated results agree reasonably with the available experimental data. According to the principles of statistic thermodynamics, thermodynamic properties were derived from the IR spectra, which were linearly correlated with the number of nitroamino groups as well as the temperature. The contributions of nitroamino groups to thermodynamic properties are in accord with the group additivity.

Theoretical Study on Vibrational Spectra, Detonation Properties and Pyrolysis Mechanism for Cyclic 2-Diazo-4,6-dinitrophenol

Based on the full optimized molecular geometrical structures at the DFT-B3LYP/6- 311＋G^＊＊ level, there exists intramolecular hydrogen bond interaction for cyclic 2-diazo- 4,6-dinitrophenol. The assigned infrared spectrum is obtained and used to compute the thermodynamic properties. The results show that there are four main characteristic regions in the calculated IR spectra of the title compound. The detonation velocities and pressures are also evaluated by using Kamlet-Jacobs equations based on the calculated density and condensed phase heat of formation. Thermal stability and the pyrolysis mechanism of 2- diazo-4,6-dinitrophenol are investigated by calculating the bond dissociation energies at the B3LYP/6-311＋G^＊＊ level.

Thermodynamics of Systems： Photopolymers-Low-Molecular Liquids

Photopolymers （printing flexoforms） during their operation interact with solvents and properties and ultimately reduces printing quality. A purpose of the work was to study the photopolymer with low-molecular liquids by two independent methods （chromatography and mathematical model of the process the thermodynamic properties and Flory-Huggins polymer-solvent systems. swell. Swelling changes the elastic thermodynamics of interaction of swelling in solvents）. By using a parameters were determined for

Synthesis, Thermal Stability and Photochemical Properties of DNA Containing Fluorescent Biaryl-Type Nucleoside Surrogates

A major goal of research in biotechnology and nanotechnology is to develop assemblies of novel biomaterials that can be used in analytical, industrial, and therapeutic applications. The synthesis of DNA （oligodeoxyribonucleotide） has been described containing the biaryl-type nucleoside surrogates, 6-deamino-2＇-deoxy-6-（l-naphthyl） adenosine （AN） and 6-deamino-2＇-deoxy-6-（1-pyrenyl） adenosine （AP）. It is found that incorporation of multiple ATM or AP residues in the middle of DNA duplexes does not significantly destabilize the duplexes and that the fluorescence intensities of the oligonucleotides containing AN or Ap significantly increases in the duplexes formed.

Giant magnetic enhancement across a ferroelectricantiferroelectric phase boundary in Bi_(1-x)Y_xFeO_3

The structural,vibrational,and magnetic properties of well prepared Bi 1 x Y x FeO 3(x=0-0.1) powders are investigated by combining the X-ray diffraction,Raman scattering,differential scanning calorimetry,and magnetometry measurements.A structural symmetric breaking from the rhombohedral R3c to orthorhombic Pnma between x=0.07 and 0.1 is identified from the X-ray and Raman measurements,accompanying a ferroelectric-antiferroelectric phase transition.The remnant magnetization of Bi 0.9 Y 0.1 FeO 3 is about 15 times higher in magnitude compared to the pure BiFeO 3.Such a giant enhancement is suggested to result from the destruction of the spin cycloid accompanied with the structured transition.