Gas phase oxidation of benzene to phenol using Pd-Cu composite catalysts. Effect of temperature,feeding gas and catalyst composition

Catalytic oxidation of benzene in the gas phase has been studied as a function of the catalyst composition, reaction temperature and the feed conditions of reactant gases, hydrogen, oxygen, benzene as well as diluting inert gas. The catalyst tested is composed of Pd and Cu(I) ions, both of which are supported on silica gel. If one of the two metal species is lacked from the catalyst, no catalytic activity appears. The product is almost exclusively phenol and some accompanying benzoquinone, in particular at lower temperatures, as minor byproduct.On leave from Hua-Dong Institute of Technology, Nanjing, People's Republic of China.     

Preparation of long sticky ends for universal ligation-independent cloning: Sequential T4 DNA polymerase treatments

Ligation-independent cloning (LIC) is a useful method for efficient directional cloning of a PCR product. LIC requires a specially designed vector containing a long stretch of sequence that is missing any one of the four nucleotides. When the linearized vector is treated with T4 DNA polymerase, in the presence of the absent base, long single-stranded overhangs are generated that are suitable for cloning. In this study, long and efficient sticky ends for LIC were produced by sequential T4 DNA polymerase treatments at non-specific sequences on a commercially available vector. All restriction enzyme sites become available in the current LIC.     

高速气流冲击式粉体表面改性装置——HYBRIDIZATION系统及应用

利用高速气流冲击法进行粉体/粉体系表面改性技术,是迄今为止各种粉体材料开发中最为引人注目的技术之一。HYBRIDIZATION(下称HYB)系统是利用高速气流冲击法对微粉体进行干式/机械化处理,是使材料复合化的最实用的装置,可对各类有机物、无机物、金属等进行广泛组合,通用性很强,适用于许多行业领域。从本文所述的系统构成、型式,有关的典型球形化处理的运转特性,利用复合化高温粉体测定被处理粉体表面温度,利用颜料改变色调等的处理特点及该系统的适用性等(一部分是从已发表的学术论文及专利上摘录的),可以说明HYB系统的概况。     

High-Temperature Active Oxidation of Chemically Vapor-Deposited Silicon Carbide in CO─CO2 Atmosphere

Active oxidation behavior of CVD-SiC in CO─CO₂ atmospheres was investigated using a thermogravimetric technique in the temperature range between 1823 and 1923 K. The gas pressure ratio, P _CO2/ P _CO, was controlled between 10⁻⁴ and 10⁻¹ at 0.1 MPa. Active oxidation rates (mass loss rates) showed maxima at a certain value of P _CO2/ P _CO, ( P _CO2/ P _CO )^*, In a P _CO2/ P _CO region lower than the ( P _CO2/ P _CO)^* a carbon layer was formed on the SiC surface. In a P _CO2/ P _CO region higher than the ( P _CO2/ P _CO)^*, silica particles or a porous silica layer was observed on the SiC surface.     

Densification of rare-earth (Lu, Gd, Nd)-doped alumina nanopowders obtained by a sol-gel route under seeding

Rare-earth (RE: Lu, Gd, Nd, 0.10 mol%)-doped alumina nanopowders were prepared by a new sol-gel route using polyhydroxoaluminum (PHA) and RECl₃ solutions under α-alumina (∼ 75 nm) seeding. Among the rare-earth dopants studied, Lu yields the most suitable nanopowders for low-temperature densification. The 0.10 mol% Lu-doped nanopowders, which were obtained at a calcination temperature of 900 °C under 5 mass% α-alumina seeding, consisted of ∼ 80-nm α-alumina particles and γ-alumina nanoparticles. Using these Lu-doped alumina nanopowders, fully densified alumina ceramics with a uniform microstructure composed of fine grains with an average size of 0.61 μm could be obtained at 1400 °C by pressureless sintering. Clearly, the Lu-doped nanopowders obtained here represent a viable option for fabricating dense, finer-grained alumina ceramics because an undoped sample with 5 mass% seeds gave a microstructure with an average grain size of 1.78 μm at 1400 °C.     

Living cationic polymerization of vinyl ethers with a functional group

Summary Vinyl ethers having oxyethylene units [CH₂=CHO-(CH₂CH₂O)-_nC₂H₅, n=1–4] were cleanly polymerized by the HI/I₂ initiator in a nonpolar solvent (toluene) at low temperatures (–15 and –40°C) to yield living-like polymers with a very narrow molecular weight distribution (Mw/Mn 1.2); the oxyethylene units in the monomers hardly disturbed the polymerization. The number-average molecular weight of the polymers increased proportionally to monomer conversion and the monomer-to-HI feed ratio. The polymerization rates of the (poly)ether-containing vinyl ethers were much greater than those of alkyl vinyl ethers under similar conditions, and it is presumed that the pendant ether oxygens intramolecularly activate the growing end. The polymers were soluble in methanol (with n1) and in water (with n2), depending on the number of oxyethylene units in the pendant.     

电子装置内的热移动研究——温度分布及速度分布

在高60cm,宽45cm 的模拟电子装置内,进行装置内热移动研究,得到不同条件下的温度分布及速度分布.在理论解析及数值计算基础上,进行无因次准数关联,得出实验式.实验结果及解析结果基本一致.利用所得实验式对正在运转或有待开发的新的电子装置有关参数进行推算,对于传热设计具有很强的实用性.     

Radical polymerization of methyl methacrylate with methyl 2,2-dimethyl-3,3-diphenyl-3-cyanopropionate as a thermal iniferter

Summary To clarify the mechanism of living radical polymerization of methyl methacrylate (MMA) with tetraphenylsuccinodinitrile (TPSN) as a thermal iniferter, a model compound for the end group of the poly(MMA) produced, methyl 2,2-dimethyl-3,3-diphenyl-3-cyanopropionate (2), was synthesized and found to initiate a living radical polymerization of MMA, indicating that the hexa-substituted C-C bond in 2 dissociated into radicals. The poly(MMA) thus obtained further initiated the radical polymerization of styrene (St) to give a block copolymer.     

Switching characteristics of vacuum gap switch employing UV‐laser triggering

The switching time and arc‐ignition probability of a sustained main discharge in a laser trigger vacuum gap were measured. The third harmonic beam of an Nd:YAG pulse laser (wavelength 355 nm, energy 5 mJ/pulse, power density 4 × 10⁷ W/cm²) was used to trigger the gap. The main electrodes 85 mm in diameter were made of oxygen‐free copper. The gap length was 1.6 mm and the experimental chamber was evacuated to about 1.3 × 10⁴ Pa by a turbomolecular pump. The UV beam from the laser was focused at normal incidence onto the grounded cathode. The switching time decreased and the arc‐ignition probability increased with increasing applied voltage. The switching time was 326 ns at 15 kV with a circuit inductance of 107 μH. Its jitter was 24.8 ns. The advantageous results obtained with the UV beam are compared to the previously reported data on triggered vacuum gaps. © 2000 Scripta Technica, Electr Eng Jpn, 132(3): 8–13, 2000     

Nondestructive inspection of thermal barrier coating of gas turbine high temperature components

A thermal barrier coating (TBC) is applied to high‐temperature components in gas turbines, and consists of a ceramic topcoat and a metallic bondcoat. Various kinds of TBC degradation and damage occur in high‐temperature components during service, such as topcoat thinning, topcoat delamination, and formation of a thermally grown oxide (TGO) layer below the topcoat, each of which can be examined using a suitable nondestructive inspection technique. Topcoat thinning can be detected by topcoat thickness measurement using terahertz waves, which are electromagnetic waves in the frequency region between optical and radio waves. The measurement resolution is about 10 μm, which is comparable to microscopic observation of the cross section in destructive inspection. Topcoat delamination can be detected by active thermography, in which the topcoat surface is scanned by a heating laser and the surface temperature distribution is measured by a thermal infrared camera. The combination of temperature peak and residual thermal image detection is effective in eliminating false detection. The TGO layer can be detected using photoluminescence, in which the Cr³⁺ ions included as an impurity in Al₂O₃ are detected. Since delamination tends to occur at locations at which the TGO layer has grown, TGO layer detection provides an effective method to select regions where delamination has occurred or is likely to occur. An inspection flow based on these techniques is proposed, which is expected to aid the establishment of condition‐based maintenance strategies of high‐temperature components. © 2016 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.