铁基超细粒子催化剂结构与还原行为的Mssbauer谱研究

铁基超细粒子催化剂具有优良的F-T反应性能。本工作利用原位Mssbauer谱辅以XRD技术研究了含有钾助剂的F-T合成铁基超细粒子催化剂的结构与还原行为,考察了催化剂组成和第二金属组分(Mn,Zn,Mg)的影响。“纯”铁超细粒子催化剂在氢气中很容易经Fe_3O_4还原为零价铁。第二金属组分的引入,一方面阻碍了催化剂的还原,另一方面稳定了Fe~(2+)的存在而使其成为还原的主要中间相,这有利于反应条件下形成类尖晶石结构的活性相。对于Fe-Mn催化剂,上述效应随锰含量的增加而更趋显著。铁基超细粒子催化剂在氢气中的还原能力依“纯”Fe>Fe-Zn>Fe-Mn>Fe-Mg的顺序递减,这在一定程度上反映了铁与第二金属组分之间相互作用的强弱。     

Selective oxidation of methanol to dimethoxymethane under mild conditions over V2O5/TiO2 with enhanced surface acidity

Dimethoxymethane was synthesized from the direct oxidation of methanol with high conversion and selectivity over specially designed bifunctional V(2)O(5)/TiO2 catalysts with redox and enhanced acidic character, in which the surface acidity played an essential role for inhibiting the formation of formaldehyde through the enhanced condensation reaction of formaldehyde with methanol to produce dimethoxymethane.     

Modification of Cr/SiO2 for the dehydrogenation of propane to propylene in carbon dioxide

Summary Dehydrogenation of propane to propylene in carbon dioxide was investigated over promoted Cr/SiO2. The results showed that the catalysts were effective for the reaction and CO2 in the feed promoted the catalytic activity. XRD, TPR and microcalorimetric adsorption techniques were used to study the structure and surface acidity of the catalysts. It was found that the surface acidity decreased with the increase of K in the Cr/SiO2 and led to the increase of selectivity toward propylene. A propane conversion of 31% with 91% selectivity to propylene over the 5%Cr-0.4%K/SiO2 catalyst was observed at 923 K with CO2 /C3H8 molar ratio of 3.6.     

神经元网络用于PCDD定量构效关系的研究

研究了不同PCDD（全名Polychlorinateddioxin）同系物分子结构的表达及特征参数的选择,应用神经元网络方法对其分子结构与色谱保留值进行了关联。对49种PCDD同系物在DWS往上不同温度下保留时间进行了预测,结果95％以上的数据点相对误差小于10％,而80％以上的数据点相对误差小于5％。     

基体辅助激光解吸电离飞行时间质谱用于寡糖的分析

将基体辅助激光解吸电离飞行时间质谱这种新兴的质谱方法用于植物中寡糖的分析。比较了不同的样品制备方法和检测方法对分析结果的影响,给出各寡糖样品的分子量分布,单体和端基基团的分子量。     

Linearization of Mach-Zehnder modulator using microring-based all-pass filter

By applying the microring resonator to the Mach-Zehnder (MZ) optical modulator and employing the super-linear phase change characteristic of the all-pass filter, the sublinear modulation curve of the conventional MZ modulator is highly linearized. With properly controlled power coupling between the microring and the arm of the MZ modulator, the third-order distortion can be suppressed. If the transmission coefficient is set between 0.25 and 0.42, the linearity range larger than 90% can be easily achieved. The maximum linearity range is even up to 99.5%.     

Preparation and properties of the single 110 K phase Bi(Pb)-Sr-Ca-Cu-O superconductor

The single 110 K phase Bi(Pb)–Sr–Ca–Cu–O superconductor was made by sintering in air. Its zero-resistance temperature is 106 K, and it is an orthorhombic cell witha=5.403 Å,b=5.412 Å andc=37.062 Å. It formed around the low-T _c phase. The forming period of the 110 K phase can be shortened by multiple sintering and grinding. If PbO is mixed into the samples after the 85 K phase has formed, the forming rate of the 110 K phase can be increased significantly. EDAX analysis of grain composition confirms that the Pb atoms enter the unit cell, and probably Pb cations replace some Ca cations.     

Communication: highly accurate ozone formation potential and implications for kinetics

Atmospheric ozone is formed by the O + O(2) exchange reaction followed by collisional stabilization of the O(3)(?) intermediate. The dynamics of the O + O(2) reaction and to a lesser extent the O(3) stabilization depend sensitively on the underlying potential energy surface, particularly in the asymptotic region. Highly accurate Davidson corrected multi-state multi-reference configuration interaction calculations reported here reveal that the minimal energy path for the formation of O(3) from O + O(2) is a monotonically decaying function of the atom-diatom distance and contains no "reef" feature found in previous ab initio calculations. The absence of a submerged barrier leads to an exchange rate constant with the correct temperature dependence and is in better agreement with experiment, as shown by quantum scattering calculations.     

Solid-Liquid Interfacial Engineered Large-Area Two-Dimensional Covalent Organic Framework Films

Constructing uniform covalent organic framework (COF) film on substrates for electronic devices is highly desirable. Here, a simple and mild strategy is developed to prepare them by polymerization on a solid-liquid interface. The universality of the method is confirmed by the successful preparation of five COF films with different microstructures. These films have large lateral size, controllable thickness, and high crystalline quality. And COF patterns can also be directly achieved on substrates via hydrophilic and hydrophobic interface engineering, which is in favor of preparing device array. For application studies, the PyTTA-TPA (PyTTA: 4,4′,4′′,4′′′-(1,3,6,8-Tetrakis(4-aminophenyl)pyrene and TPA: terephthalaldehyde) COF film has a high photoresponsivity of 59.79 μA W⁻¹ at 420 nm for photoelectrochemical (PEC) detection. When employed as an active material for optoelectronic synaptic devices for the first attempt, it shows excellent light-stimulated synaptic plasticity properties such as short-term plasticity (STP), long-term plasticity (LTP), and the conversion of STP to LTP, which can be used to simulate biological synaptic functions.     

Research of Asymmetric Y-Branching Total Internal Reflection All-Optical Switch

Y-branching TIR all-optical switch have been fabricated. When the switching optical intensity is 149.9W/mm2, the extinction ratio is 18dB. A theoretical model was also proposed which provided a good fit to the experimental data.