激光触发SF6-N2混合气体开关的数值模拟

 在气体放电物理的基础上，对SF₆和N₂采用双光子电离模型，对碳氢化合物的光电离采用3能级模型，并考虑了混合气体的热电离和激光对气体的欧姆加热作用，建立了激光触发SF₆-N₂混合气体开关的数值模型，模拟了激光触发SF6-N2混合气体多级间隙开关实验。激光触发延迟时间的计算值与实验结果符合较好。理论计算表明：激光触发SF₆-N₂混合气体间隙开关的延迟时间随SF₆含量的增加呈上升趋势，而随激光脉冲能量、充气压力等的上升呈下降趋势。     

Smaller Output Beam Divergence in the Slowly Opened Q-Switch Operation

The mechanism of the slowly opened Q-switch operation was investigated thoroughly. Maximum energy extraction from the resonator could be optimized, and the smallest output beam divergence could be achieved. In this article, we present a detailed analysis that has numerically verified the mode-selection mechanism in the slowly opened Q-switch operation, and the degree of the smaller output laser beam divergence that has been achieved. The mechanism of the slowly opened Q-switch operation is the inherent advantage of the passive saturable absorber in this operation. We can use the maximum energy extraction and the smallest output beam divergence results of the slowly opened Q-switch operation to design and optimize various passive saturable absorbers: plastic dye sheets, LiF:F₂⁻ color center crystals, Cr4⁺: YAG crystals, RG1000 color glass filters, and the single crystal semiconductor saturable absorber wafers that are in developed in our microchip laser systems.     

Planned positron experiments at FRM-II

The new research reactor FRM-II near Munich has a strong positron source, which delivers an intense, nearly monoenergetic positron beam. Our positron systems, the pulsed low energy positron source (PLEPS) and the scanning positron microscope (SPM) will be operated at this beam. Some aspects of matching these systems to the new positron source will be discussed.Considerable improvements are expected, e.g. more than 10⁵ s⁻¹ recorded events at PLEPS and sub-micrometre resolution at SPM. They will enable investigations in so far inaccessible problems like the evaluation of annihilation characteristics and trapping constants of individual defects or studies of fast dynamical processes. In applied materials science complex defect structures will be studied which demand a resolution into many differing lifetimes, e.g. fractured specimens, wear, corrosion, etc. Also large series of measurements at small systematic modifications are planned. There is also the opportunity to analyse in addition the chemical microstructure of the specimens by means of a hydrogen microprobe and other ion beam techniques available close to FRM-II at the Technical University of Munich.     

Matrix assisted pulsed laser evaporation processing of triacetate-pullulan polysaccharide thin films for drug delivery systems

We report the first successful deposition of triacetate-pullulan polysaccharide thin films by matrix assisted pulsed laser evaporation. We used a KrF* excimer laser source (λ = 248 nm, τ ≈ 20 ns) operated at a repetition rate of 10 Hz. We demonstrated by FTIR that our thin films are composed of triacetate-pullulan maintaining its chemical structure and functionality. The dependence on incident laser fluence of the induced surface morphology is analysed.     

甲烷分子在碱性催化剂上的吸附与酸碱活化机理

以碳酸锶为甲烷吸附活化的模型催化剂，用切换变应答、ＣＨ４（ＣＯ２）－ＴＰＤ等技术，对甲烷的吸附、碱性对催化剂性能的影响进行了研究，结果表明，甲烷在碳酸锶上的活化显示出明显的酸碱活化机理特征，瞬变应答及ＴＰＤ结果均证明，甲烷在碳酸锶表面有较强的吸附，其脱附温度约３１０℃，关联结果表明，甲烷转化率及Ｃ２烃收率与催化剂表面ＳｒＯ碱性中心浓度有非常一致的顺变关系，因此催化剂表面的酸碱中心可能是甲烷的选择活     

磺化酞菁铜分子膜／SiO2／Si界面电荷转移机制的研究

在具有不同氧化层厚度的p型硅基片上修饰2层磺化酞菁铜分子膜.利用时间分辨表面光电压谱技术,对该膜系的界面电荷转移机制的光电开关特性进行了研究。结果表明,用时间分辨表面光电压谱技术研究界面电荷转移过程具有明显优越性.     

蒽环与苯环间的光化学Ⅰ.蒽环与苯环间分子内光致环加成反应

9 氯甲基蒽 ( 1 )与 3 ,5 二甲氧基苄醇 ( 2 )在相转移催化剂存在下反应生成 9 ( 3 ,5 二甲氧基苄基氧甲基 )蒽 ( 3 ) .( 3 )的苯溶液在紫外光照射下发生蒽环与苯环间的分子内 [4π + 4π]光致环加成反应 ,定量地生成多环化合物 ( 4 ) .( 4 )在热的作用下发生逆反应 ,定量地转化成原料 ( 3 ) .这种光致可逆反应可应用于制备光开关材料 .     

Thermodynamic molecular switch in sequence‐specific hydrophobic interactions

This communication will demonstrate the existence of a thermodynamic molecular switch in the pairwise, sequence‐specific hydrophobic interaction of Ile–Ile, Leu–Ile, Val–Leu, or Ala–Leu over the temperature range of 273–333 K reported by Nemethy and Scheraga in 1962. Based on Chun's development of the Planck–Benzinger methodology, the change in inherent chemical bond energy at 0 K, ΔH°(T₀), is 3.0 kcal mol^?1 for Ile–Ile, 2.4 for Leu–Ile, 1.8 for Val–Leu, and 1.2 kcal mol^?1 for Ala–Leu. The value of ΔH°(T₀) decreases as the length of the hydrophobic side chain decreases. It is clear that the strength and stability of the hydrophobic interaction is determined by the packing density of the side chains, with Ala–Leu being the most stable. At 〈T_m〉, the thermal agitation energy, $\int^{T}_{0}\Delta Cp^{\circ}(T)\,dT$, is about five times greater than ΔH°(T₀) in each case. Additionally, the thermal agitation energy for the same series, evaluated at 〈T_m〉, decreases in the same order, that is, as the length of the side chain decreases. This pairwise, sequence‐specific hydrophobic interaction is highly similar in its thermodynamic behavior to that of other biological systems, except that the negative Gibbs free energy change minimum at 〈T_s〉 occurs at a considerably higher temperature, 355 K compared to about 300 K. The melting temperature, 〈T_m〉, is also high, 470 K compared to 343 K in a biological system. The implication is that the negative Gibbs free energy minimum at a well‐defined 〈T_s〉 has it origin in the hydrophobic interactions, which are highly dependent on details of molecular structure. In addition to the four specific dipeptide interactions described, we have shown in our unpublished work the existence of a thermodynamic molecular switch in the interactions of 32 dipeptides wherein a change of sign in ΔCp°(T)_reaction leads to a true negative minimum in the Gibbs free energy of reaction, and hence, a maximum in the related K_eq. Indeed, all interacting biological systems that we have thus far examined using the Planck–Benzinger approach point to the universality of thermodynamic molecular switches. © 2001 John Wiley & Sons, Inc. Int J Quantum Chem, 2001     

脉冲电晕环境中13X分子筛对NO分解作用的研究

在常温、常压下，利用脉冲电晕放电产生冷等离子体，使一氧化氮发生分解，直接生成氮气和氧气，用四极杆质谱仪在线测量反应过程中反应物和生成物的变化。在自行研制的实验台上，考察了13X分子筛在不同的脉冲电晕放电条件下，表现出来的不同特性及其对反应转化率的影响。在30 ℃～430 ℃、流量375 mL/min～1 333 mL/min，分析了该反应过程中13X分子筛对转化率的促进作用。在同一脉冲放电条件下，控制13X分子筛的温度为200 ℃，转化率从30 ℃时的1.2%上升到19.7%；转化率最高可以达到35.9%。并对反应过程中13X分子筛的吸附特性做了初步探讨。     

Diagnosis of OH Radical by Optical Emission Spectroscopy in Atmospheric Pressure Unsaturated Humid Air Corona Discharge and its Implication to Desulphurization of Flue Gas

OH radical in the corona discharge with pipe–nozzle–plate electrode has been diagnosed by optical emission spectroscopy. Spatial variations of OH radical emission in discharge gap have been measured. Relative intensity of OH radical emission spectroscopy increases with increasing water vapor flux injected into the reactor or intensity of electric field supported. In positive pulsed corona discharge, relative intensity is higher than that in positive DC corona discharge and lower than that in negative DC corona discharge. Strongest intensity of OH radical spectrum appears within the range of 5 mm near the discharge nozzle- electrode. In addition, it is proved that the efficiency of desulphurization from flue gas by pulsed corona discharge plasma processes can be improved when OH radical is produced in the reactor.