SD对壳模型: 偶偶Pt核低激发态性质

利用SD对壳模型讨论了偶偶Pt核低激发态的集体性质. 结果发现在该模型下, 利用一个仅含有3个参数的哈密顿量, 可以很好地再现偶偶Pt核低激发谱的集体性质.     

Kinetic theory of high-relativistic electron cyclotron maser with anovel quasioptical cavity

Using the Laplace transformation, the kinetic theory of the high-relativistic electron cyclotron maser having a novel open-resonator-the axisymmetrical quasioptical cavity of oblique rotation at arbitrary angle, is carried out within the framework of the linearized Vlasov-Maxwell equations. The beam-wave interaction power, starting current and frequency shift have been derived and numerically calculated. The influence of rotation angle on the beam-wave interaction is also studied. A series of important conclusions obtained reveal the characteristics of this novel quasioptical electron cyclotron maser     

产生短间隔高精度纳秒激光双脉冲的实用电路

本文介绍了我们研制的“运动粒子瞬态激光全息测试仪”电子线路.该电路经严格的逻辑设计及计算,采用了10MHz时钟电路,并将1MHz的时钟信号巧妙地引入门控电路中,同时在技术上采用了行之有效的措施,消除了可能产生0.1μs的随机误差,时间间隔达到了(1～9)±0.1μs的精度,所输出的激光双脉冲能量接近,整机抗干抗能力强,一次性试验成功率高,可精确地测量雾化粒子场中的微粒的速度、形状、大小及其分布,收到了良好的使用效果.     

NiTi合金相变过程中界面动力学的内耗研究

本文采用同时测量内耗、模量及电阻的方法,对NiTi合金变温过程中所发生的正、反马氏体相变及可逆I/C相变进行了系统的研究。结果表明,变温马氏体相变及I/C相变过程中内耗均为粘弹性型内耗,是相界面在克服粘滞性阻力而运动时引起的。从界面动力学出发,研究了相变过程中界面的运动动力学行为。由实验数据求得了马氏体相变过程中界面动力学关系的具体表达式为:V=V^*exp(—△G^*/△G—△G_R);相变过程内耗表达式为:Q^-1=(n²)/2·(μ△G^*)/((△G—△G_R)²)·(dF)/(dT)·T/ω;相变阻力△G_R约为10cal/mol的数量级。讨论了相变过程中的“软模”效应。马氏体相变过程中的模量“软化”来自声子模的软化和界面运动引起的附加模量亏损两个方面。 关键词：     

On N-widths in Ip

In this paper we prove that (1<p<+∞), give the characteristics of x^o and the optimal subspace for n-width d_n in space X=l _n ^N . Where d_n in the n-width, in the sense of Kolmogorov, ofD in X, dⁿ is the n-width ofD with respect to X, in the sense of Gel'fand, δ is the linear n-width ofD with respect to X.     

苯部分加氢制环己烯的非晶态Ru-M-B/ZrO2催化剂的表征

采用化学还原法，制备了高活性，高选择性非晶态RU-M-B/ZRO2催化剂，并将其用于催化苯部分加氢制环己烯，在140℃、5.0Mpa氢压下，苯转化40%时，环己烯选择性达到85%左右。环己烯最高收率达到52.1%，用XRD、SEM、BET比表面积测定等手段对摧化剂进行表征，XRD和SEM测试表明，RU-U-B/ZRO2属于非晶态，活性组分高度分散，XRD结果证实，在加氢过程中，非晶分解，RU晶化；温度愈高，RU晶化愈快，催化剂的活性、选择性与RU微晶的粒径有关，RU微晶粒径应控制在5nm左右，BET比表面积测定表明，ZRO2的负载提高了催化剂的比表面积，从而有利于活性组分的高度分散，并可阻止RU微晶的长大，讨论了B和ZRO2对提高选择性的作用。     

Covalent attachment of phospholipid analogous polymers to modify a polymeric membrane surface: a novel approach

A novel method for the surface modification of a microporous polypropylene membrane by tethering phospholipid analogous polymers (PAPs) is given, which includes the photoinduced graft polymerization of N,N-dimethylaminoethyl methacrylate (DMAEMA) and the ring-opening reaction of grafted poly-(DMAEMA) with 2-alkyloxy-2-oxo-1,3,2-dioxaphospholanes. Five 2-alkyloxy-2-oxo-1,3,2-dioxaphospholanes, containing octyloxy, dodecyloxy, tetradecyloxy, hexadecyloxy, and octadecyloxy groups in the molecular structure, were used to fabricate the PAP-modified polypropylene membranes. The attenuated total reflectance FT-IR spectra of the original, poly(DMAEMA)-grafted, and PAP-modified membranes confirmed the chemical changes on the membrane surface. Scanning electron microscope pictures showed that, compared with the original membrane, the surface porosities ofpoly(DMAEMA)-grafted and PAP-modified membranes were somewhat reduced. Water contact angles measured by the sessile drop method on PAP-modified membranes were slightly lower than that on the original polypropylene membrane, but higher than those on poly(DMAEMA)-grafted membranes with the exception of octyloxy-containing PAP-modified membranes. However, BSA adsorption experiments indicated that the five PAP-modified membranes had a much better protein-resistant property than the original polypropylene membrane and the poly(DMAEMA)-grafted membranes. For hexadecyloxy- and octadecyloxy-containing PAP-modified membranes, almost no protein adsorption was observed when the grafting degree was above 6 wt %. It was also found that the platelet adhesion was remarkably suppressed on the PAP-modified membranes. All these results demonstrate that the described approach is an effective way to improve the surface biocompatibility for polymeric membranes.     

过渡金属钼钒砷杂多化合物的合成与TPR,TPD研究

Seven transition metal molybdovanadoarsenic heteropoly compounds have been synthesized and characterized using IR, UV, TG-DTA, pH potential titration techniques. The molecular formulae of these compounds are pro-posed to be H_xM_yAsMO₁₀V₂O₄₀·zH₂O(x=1～3, y=1,2, M=Cr, Mn, Fe, Co, Ni, Cu, Zn).They are all keggin structure. Surface nature of these compounds have been investigated by temperature programmed desorption and temperature programmed reduction techniques. NH₃-TPD results show that in TPD profiles of the compounds there are two desorption peaks corresponding to weak acid sites of desorption, respectively. Desorbing activativon energy and preexponential factor of weak acid site of desorption for compounds have been calculated. H₂-TPR re-sults show that introducting transtion metal to molybdovanarsenic acid, the reduction peak temperatures of H₂-TPR shift regularly with increasing d electron numbers of transition metals. In addition, Zn and Cu heteropoly com-pounds have yet apparent effect of hydrogen spill over.