高气压大电流放电条件下的电极烧蚀

归纳了影响开关电极烧蚀量的因素,包括开关电极材料、放电条件等,分析了开关电极烧蚀特征与烧蚀后表面形貌,总结了开关电极烧蚀的主要机制电极加热和电极材料去除机制。为了延长开关工作寿命,提出了减少开关电极烧蚀的措施,包括选用抗烧蚀性能优异的材料作为开关电极材料、采用合适的开关电极结构和优化的放电条件等。     

Numerical investigations of supercavitation around blunt bodies of submarine shape

Cavitation occurs when liquid is subjected to rapid changes of pressure. If the local pressure is lower than the liquid saturation pressure, the liquid changes its phase into vapor. A fast moving solid body underwater will reduce the local pressure around the body. Under certain conditions, the local pressure can be lower than the water saturation pressure, accordingly causing cavitation. If the velocity of the moving body increases further, a supercavitation will occur. In this paper, the cavitation and supercavitation were studied by the SST k–ω turbulence model combined with a finite-rate mass transfer modeling under the mixture assumption. The validations of these models were performed through comparisons between numerical simulations and experiments. After the validations, the supercavitation generated by a high speed moving body, which can be described as a large bubble, was studied. The studies were on several blunt bodies, such as a submarine hull shape, a submarine hull shape with appendages and a full submarine shape with sail and appendages. It was found that the naked submarine hull is difficult to have the supercavitation covering the whole body. The sail and appendages can help supercavitation occurs earlier. Furthermore the effects of the supercavitation on the submarine and generation mechanism of the supercavitation is discussed based on the simulations.     

不同线宽结构杂散光Kirk模型分析

采用Kirk测量法的杂散光模型研究了杂散光在不同线宽结构上杂散光的光强变化,通过图像对比度分析了杂散光对不同线宽结构的影响。基于Matlab软件仿真分析表明:线宽一定时,线条越稀疏,图像对比度越低,杂散光对成像图形分辨力的影响越大;线条线间比一定时,线宽尺寸越小,图像对比度越低,杂散光对成像图形分辨力的影响也越大。所以杂散光对线宽较小并且线条稀疏空间结构所成的图形造成的影响较大。光刻; Kirk测量法; 杂散光; 点扩散函数; 图像对比度     

Brugnanin,a new syn-2,3-dihydrobenzofuran neolignan dioate from the mangrove <Emphasis Type="Italic">Bruguiera gymnorrhiza</Emphasis>

Brugnanin (1), a neolignan dioate, was isolated from a mangrove plant Bruguiera gymnorrhiza. Based on spectroscopic interpretation of MS, IR, and NMR data, 1 was elucidated as (7R*,8S*,E)-3-hydroxy-5,5′-dimethoxy-7-O-4′,8-3′-neolignan-7′-ene-9,9′-dioic acid dioctadecyl ester. MTT assay showed that 1 had weak inhibitory activity against growth of CNE-1 nasopharyngeal carcinoma cell line. Published in Khimiya Prirodnykh Soedinenii, No. 2, pp. 147–149, March–April, 2008.     

Generation of Glycosyl Radicals from Glycosyl Sulfoxides and Its Use in the Synthesis of C‐linked Glycoconjugates

We here report glycosyl sulfoxides appended with an aryl iodide moiety as readily available, air and moisture stable precursors to glycosyl radicals. These glycosyl sulfoxides could be converted to glycosyl radicals by way of a rapid and efficient intramolecular radical substitution event. The use of this type of precursors enabled the synthesis of various complex C‐linked glycoconjugates under mild conditions. This reaction could be performed in aqueous media and is amenable to the synthesis of glycopeptidomimetics and carbohydrate‐DNA conjugates.     

Synthesis and Characterization of 2-[(3-Aminophenyl)sulfonyl] ethanol Hydrogen Sulfate

2-[(3-Aminophenyl)sulfonyl] ethanol hydrogen sulfate (APSES) is an important intermediate for reactive dyes.It can be used to synthesize KN type reactive dyes, which have broad colour spectra,good water solubility, excellent adaptability for different dye technique,etc. Synthesis of APSES were currently developed by Kato Kuniok et al^[1] and Sanki^[2].Kato had attempted to synthesize of APSES by reaction of sodium benzenesulfinate as raw material with ethylene oxide to obtain 2-phenylsulfonyl ethanol(PSE). The PSE could further be nitrated and hydrogenated to obtain 2-[(3-aminophenyl)sulfonyl]ethanol (APSE). Finally,APSE was reacted with oleum to obtain 2-[(3-aminophenyl) sulfonyl] ethanol hydrogen sulfate (APSES). Sanki had discoved a new synthetic method for the PSE. The PSE was prepared by first reaction of thiophenol as raw material with chloroethanol, and then by oxidation with hydrogen peroxide.The above mentioned two methods are not easily be adopted in industries at home. The shortage and cost of the thiophenol and sodium benzenesulfinate are mainly limited. We modificated a new synthetic pathway for APSES by five steps. The experimental procedures are shown the following.     

Heterogeneous reaction of SO2 on TiO2 particles

The heterogeneous reaction of SO₂ on TiO₂ particles was studied using in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The influences of the oxygen concentration, relative humidity (RH), and ultraviolet (UV) light illumination (λ ≈ 365 nm) intensity on the reaction were investigated. The main product of the heterogeneous reaction of SO₂ on TiO₂ particles was sulfate with UV illumination and sulfite without it. The production of sulfate was promoted significantly with UV illumination or water, and there was a synergistic effect when both were present. In the dry system without UV, the heterogeneous reaction of SO₂ on TiO₂ particles was found to be second-order for SO₂ and the initial uptake coefficient, γ_BET, was determined to be 1.94 × 10^?6. With UV and RH = 40%, the reaction order was first-order and the initial uptake coefficient was 1.35 × 10^?5.     

Phosphorous,nitrogen, and molybdenum ternary co-doped TiO2: preparation and photocatalytic activities under visible light

P, N, and Mo ternary co-doped nano TiO₂ photocatalysts ((P, N, Mo)-TiO₂) were prepared by a single step sol–gel method, which show much enhanced photocatalytic activities over Mo-TiO₂, (P, N)-TiO₂, un-doped TiO₂ and Degussa P25 under visible light irradiation. The degradation rate of 0.72Mo–P-TiO₂ is as high as 65.3%, which is about 6.7 times of that of Degussa P25. Possible reasons for the improvement of photocatalytic activities were analyzed.     

Mesoporous inorganic salts with crystal defects: unusual catalysts and catalyst supports

We proposed a strategy to synthesize mesoporous inorganic salt particles using the special properties of ionic liquid (IL) mixtures, and hollow mesoporous LaF₃, NdF₃, and YF₃ particles were synthesized and characterized using different techniques. The size of the mesopores in the salt particles was about 4 nm, and the materials were full of crystal defects. The LaF₃, NdF₃ and YF₃ particles were used as the catalysts for the cyanosilylation reaction of benzaldehyde using trimethylsilyl cyanide, and Ru/LaF₃ and Ru/NdF₃, in which Ru nanocatalysts were supported on the LaF₃ and NdF₃ particles with mesopores, were used to catalyze hydrogenations of benzene to cyclohexane and levulinic acid (LA) to γ-valerolactone (GVL). It was discovered that the activities of these catalysts were unprecedentedly high for these reactions. Detailed study showed that both the crystal defects and the mesopores in the salt particles played crucial roles for the extremely high catalytic activity.     

Dynamics of ice nucleation on water repellent surfaces

Prevention of ice accretion and adhesion on surfaces is relevant to many applications, leading to improved operation safety, increased energy efficiency, and cost reduction. Development of passive nonicing coatings is highly desirable, since current antiicing strategies are energy and cost intensive. Superhydrophobicity has been proposed as a lead passive nonicing strategy, yet the exact mechanism of delayed icing on these surfaces is not clearly understood. In this work, we present an in-depth analysis of ice formation dynamics upon water droplet impact on surfaces with different wettabilities. We experimentally demonstrate that ice nucleation under low-humidity conditions can be delayed through control of surface chemistry and texture. Combining infrared (IR) thermometry and high-speed photography, we observe that the reduction of water-surface contact area on superhydrophobic surfaces plays a dual role in delaying nucleation: first by reducing heat transfer and second by reducing the probability of heterogeneous nucleation at the water-substrate interface. This work also includes an analysis (based on classical nucleation theory) to estimate various homogeneous and heterogeneous nucleation rates in icing situations. The key finding is that ice nucleation delay on superhydrophobic surfaces is more prominent at moderate degrees of supercooling, while closer to the homogeneous nucleation temperature, bulk and air-water interface nucleation effects become equally important. The study presented here offers a comprehensive perspective on the efficacy of textured surfaces for nonicing applications.