Synthesis and Crystal Structure of 3,9-Bis（pyridin-2-yl）-2,4,8,10-tetraoxaspiro[5.5]undecane

The title compound 3,9-bis(pyridin-2-yl)-2,4,8,10-tetraoxaspiro[5.5]undecane 4(C17H18N2O4) has been synthesized by the reaction of 2,2-bis(hydroxymethyl)propane-1,3-diol with pyridine-2-carbaldehyde in the presence of p-toluenesulfonic acid,and characterized by IR,1H-NMR and X-ray single-crystal diffraction.The crystal belongs to monoclinic system,space group C2/c with a = 25.133(2),b = 5.7219(5),c = 21.942(2) ,β = 99.145(2)°,V = 3115.3(5)3,Z = 8,Dc = 1.340 g/cm3,Mr = 314.33,F(000) = 1328,μ = 0.097 mm-1,MoKa radiation(λ = 0.71073),R = 0.0352 and wR = 0.1022 for 2486 observed reflections with I > 2σ(I).X-ray analysis reveals that the two 1,3-dioxane rings passing through the central spiro-C atom both adopt chair conformation.Intermolecular C-H…π,C-H…O and C-H…N weak interactions link the molecules to form a three-dimensional samdwich,which are effective in the stabilization of the crystal structure.     

应用于高速转子系统的金属橡胶阻尼环动力特性分析

针对金属橡胶构件的非线性特性及结构不同时弹性阻尼力学性能不同的特点, 利用实验和理论相结合的方法建立了金属橡胶构件迟滞回线边界变形过程力学模型, 推导了不同相对密度金属橡胶构件非线性迟滞恢复力表达式. 分析了简谐激励载荷作用下金属橡胶阻尼环动力学特性, 对该阻尼环进行了实验研究, 研究了存在预变形情况下阻尼环的弹性阻尼性能, 实验和理论分析结果基本一致, 为该种阻尼环的实际应用奠定了理论基础. 关键词： 金属橡胶构件 力学模型 非线性迟滞恢复力     

一种基于~4He气闪烁体的裂变中子探测器

研制了一种新中子探测器,它以²³⁵UO₂裂变靶作为转换靶,⁴He气体作为闪烁体.该探测器充分结合了²³⁵U和⁴He两种核素的特点,从而具有中子能量响应平坦、中子灵敏度较高、n/γ分辨本领高等优点,能很好地在混合脉冲裂变辐射场中测量中子.本文对探测器的原理和结构设计进行了介绍,计算了不同能量中子、γ射线在探测器中的能量沉积,并从理论和实验上对探测器的中子灵敏度、γ射线灵敏度、n/γ分辨本领和时间响应进行了研究.结果表明探测器的中子灵敏度约10^-15C·cm²,γ灵敏度约10^-17C·cm²,时间响应约33.1 ns.     

Research on surface photovoltage spectroscopy for GaAs photocathodes with AlxGa1-xAs buffer layer

Surface photovoltage spectroscopy equations for cathode materials with an AlxGa1-x As buffer layer are determined in order to effectively measure the body parameters for transmission-mode (t-mode) photocathode materials before Cs-O activation.Body parameters of cathode materials are well fitted through experiments and fitting calculations for the designed AlxGa1-x As/GaAs structure material.This investigation examines photo-excited performance and measurements of body parameters for t-mode cathode materials of different doping structures.It also helps study various doping structures and optimize structure designs in the future.     

Irreversibility of a quantum walk induced by controllable decoherence employing random unitary operations

Quantum walk is different from random walk in reversibility and interference. Observation of the reduced re- versibility in a realistic quantum walk is of scientific interest in understanding the unique quantum behavior. We propose an idea to experimentally investigate the decoherence-induced irreversibility of quantum walks with trapped ions in phase space via the average fidelity decay. By introducing two controllable decoherence sources, i.e., the phase damping channel (i.e., dephasing) and the high temperature amplitude reservoir (i.e., dissipation), in the intervals between the steps of quantum walk, we find that the high temperature amplitude reservoir shows more detrimental effects than the phase damping channel on quantum walks. Our study also shows that the average fidelity decay works better than the position variance for characterizing the transition from quantum walks to random walk. Experimental feasibility to monitor the irreversibility is justified using currently available techniques.     

Comparative research on the transmission-mode GaAs photocathodes of exponential-doping structures

Early research has shown that the varied doping structures of the active layer of GaAs photocathodes have been proven to have a higher quantum efficiency than uniform doping structures.On the basis of our early research on the surface photovoltage of GaAs photocathodes,and comparative research before and after activation of reflection-mode GaAs photocathodes,we further the comparative research on transmission-mode GaAs photocathodes.An exponential doping structure is the typical varied doping structure that can form a uniform electric field in the active layer.By solving the one-dimensional diffusion equation for no equilibrium minority carriers of transmission-mode GaAs photocathodes of the exponential doping structure,we can obtain the equations for the surface photovoltage(SPV) curve before activation and the spectral response curve(SRC) after activation.Through experiments and fitting calculations for the designed material,the body-material parameters can be well fitted by the SPV before activation,and proven by the fitting calculation for SRC after activation.Through the comparative research before and after activation,the average surface escape probability(SEP) can also be well fitted.This comparative research method can measure the body parameters and the value of SEP for the transmission-mode GaAs photocathode more exactly than the early method,which only measures the body parameters by SRC after activation.It can also help us to deeply study and exactly measure the parameters of the varied doping structures for transmission-mode GaAs photocathodes,and optimize the Cs-O activation technique in the future.     

Hydrogen adsorption and desorption on the Pt and Pd subnano clusters – a review

In this review, we present our recent first principles studies on the sequential H₂ dissociative chemisorption and H desorption on the Pt_n and Pd_n clusters (n=2-9, 13). Upon full saturation by H atoms, the calculated H₂ dissociative chemisorption energy and H desorption energy on Pt₁₃ and Pd₁₃ clusters are similar to the corresponding values on smaller close-packed clusters. Indeed, the catalytic performances of these subnano clusters do not vary significantly with the particle sizes or shapes. Instead, they are dependent on the surface metal atoms which can be accessed by H atoms. In addition to the coverage dependency of the H₂dissociative chemisorption and H sequential desorption energies, the phase transition of both Pt₁₃ and Pd₁₃from the icosahedral to fcc-like structures at certain H coverage was also investigated.     

SHPB实验中粘弹性试件内部应力波的传播

建立描述SHPB实验中线性粘弹性试件内部应力波传播的控制方程组,根据试件两端与入射杆及透射杆接触的应力波特征关系给出耦合边界条件.对方程组和定解条件进行Laplace变换,求得试件内部应力在变换域像函数的表达式.采用数值反变换技术进行反Laplace变换,获得试件两端的应力时程曲线.对现有的固定Tal-bot反变换算法进行改进:将入射波像函数分解为基本部分和延迟部分,利用固定Talbot算法对基本部分入射波作用下的波动问题求解,其他部分的解通过延迟定理得到,最终解为两部分的叠加.采用这种改进算法得到的不同入射波下粘弹性试件的内部应力解与传统的基于特征线数值模拟方法的结果吻合.在此基础上探讨了粘弹性试件的几何参数和材料本构参数对透射波波形的影响.     

145Er的β延发质子衰变性质研究

通过92Mo(58Ni, 2p3n)熔合蒸发反应生成了非常缺中子核145Er。利用氦喷嘴带传输系统把研究目标核传输到低本底测量站, 进行了质子 γ符合测量, 得到了不受同量异位素干扰的145Er的β延发质子谱。经过仔细分析与延发质子符合的γ谱, 发现了145Er的11/2-同核异能态具有β延发质子衰变性质。经拟合退激144Dy不同激发态γ跃迁的衰变曲线, 得出145Er的1/2+基态和11/2-同核异能态的半衰期分别为(1.6±0.6)和(0.6±0.1) s。最后, 简单介绍了中重质量区缺中子新核素的合成及衰变研究计划。The neutron deficient isotope 145Er was produced via the fusion evaporation reaction 92Mo(58Ni, 2p3n). The reaction products were transported to a low background counting area using a He jet tape transport system, and proton γ coincidence measurements were carried out. Based on the analysis of γ transitions in coincidence with β delayed protons, the β delayed proton decay of an νh11/2 isomer in 145Er was proposed. By fitting the decay curves of the γ transitions depopulating the low lying states in 144Dy, the half lives of the ground state and the νh11/2 isomeric state in 145Er were deduced to be (1.6±0.6) and (0.6±0.1) s, respectively. An experimental plan to synthesize new β delayed proton precursors in the medium heavy mass region has been presented.     

头孢唑啉酸与稀土元素Eu3+配合物的合成及配位位置的研究

头孢唑啉酸(cefazolin)为抗生素类药物,它的钠盐就是通常所说的先锋霉素. 我们通过共沉淀法合成了头孢唑啉酸与稀土元素Eu³⁺ 的固体配合物,并对其进行了光谱及波谱研究. 通过IR、¹H NMR和¹³C NMR确定了配合物的配位点,并探讨了配位机理.