聚变反应历程测量系统研制及应用

为了测量惯性约束聚变实验中的聚变反应时间过程,研制了一套时间分辨优于40 ps的聚变反应历程测量系统.该系统由闪烁体及鼻锥部分、光学系统和条纹相机系统三部分组成.其中闪烁体将中子信号转换为可见光信号,光学系统则将闪烁体的发光信号成像在条纹相机上进行记录.为得到信号与入射激光的时间关系,还将时标引入了条纹相机进行记录.在...     

辐射驱动条件下冲击波诊断用透明窗口离化现象研究

针对间接驱动情况下,冲击波诊断中出现的X光离化问题,利用半导体模型,解释了蓝宝石和石英晶体材料中出现黑区的理论过程,并进行了实验验证.利用光生载流子模型分析了石英晶体中时间方向上出现调制的过程,并进行了实验验证.发现使用石英晶体作为窗口材料,使用60μm厚度的烧蚀层,在180 eV辐射温度条件下,没有出现明显的黑区.使...     

Persistence and extinction of a stochastic logistic model with delays and impulsive perturbation

A stochastic logistic model with delays and impulsive perturbation is proposed and investigated. Sufficient conditions for extinction are established as well as nonpersistence in the mean, weak persistence and stochastic permanence. The threshold between weak persistence and extinction is obtained. Furthermore, the theoretical analysis results are also derivated with the help of numerical simulations.     

Spectral collocation method for linear fractional integro-differential equations

In this paper, we propose and analyze a spectral Jacobi-collocation method for the numerical solution of general linear fractional integro-differential equations. The fractional derivatives are described in the Caputo sense. First, we use some function and variable transformations to change the equation into a Volterra integral equation defined on the standard interval [-1,1]$[-1\text{,}1]$. Then the Jacobi–Gauss points are used as collocation nodes and the Jacobi–Gauss quadrature formula is used to approximate the integral equation. Later, the convergence order of the proposed method is investigated in the infinity norm. Finally, some numerical results are given to demonstrate the effectiveness of the proposed method.     

富勒烯在溶液和有机玻璃薄膜中的吸收光谱研究

利用在甲苯中溶解富勒烯与有机玻璃（ＰＭＭＡ）的方法，我们分别制得了掺Ｃ６０以及掺Ｃ７０有机玻璃薄膜．分别研究了Ｃ６０和Ｃ７０在溶液、有机玻璃薄膜两种不同状态下的吸收光谱，实验结果表明：有机玻璃这种固态环境对富勒烯的吸收特性影响很小，富勒烯在有机玻璃薄膜中的吸收曲线同在溶液状态时基本相同．Ｃ６０在有机玻璃薄膜中的吸收峰相对于溶液中峰位略有红移，但Ｃ７０的情况则刚好相反，它在前者的吸收峰相对于后者峰位蓝移，分析了产生这种现象的原因     

Thiol‐ene photopolymerization for efficient curing of vinyl esters

Monomers for radical photopolymerization based on vinyl esters (VEs) have recently been identified as suitable alternatives to (meth)acrylates on account of their low irritancy and cytotoxicity. The drawback of most VEs with abstractable hydrogens is their relatively low reactivity compared with (meth)acrylates. Within this article, we proved by photo‐differential scanning calorimetry measurements and real‐time Fourier transform infrared spectroscopy that the thiol‐ene concept is able to improve the photoreactivity of these VEs to a large extent to a level between those of acrylates and methacrylates. Other VEs have now a reactivity of at least the level of similar acrylates. Mechanical properties as determined by Dynamic Mechanical Analysis and Charpy impact tests showed significant toughening of these materials. Furthermore, we were able to confirm low toxicity of all components by osteoblast cell culture experiments. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Hydrothermal Synthesis and Primary Gas Sensing Properties of CuO Nanosheets

Uniformity nanosheets of CuO were prepared by a mild hydrothermal synthesis method. Phase analysis was carried out using x-ray diffraction (XRD) and the result confirmed the CuO nanosheets as a single phase. The field-emission scanning electron microscopy (FE-SEM) was used to observe the morphology of CuO nanosheets while the gas sensing properties of these unique CuO nanosheets were tested at a static state system. The results show that the CuO has uniformity nanosheets, and the gas sensing property show that the CuO nanosheets gas sensor has a stable gas response and the same gas sensitivity trend to tested gases. This method may be suitable for larger-scale production of these CuO nanosheets for practical applications.     

Asymmetric synthesis of multi-substituted spiro[5,5]undecane-1,5,9-triones via organocatalytic three-component reaction

The asymmetric domino three-component Knoevanagel-Diels-Alder addition (ATCDA) reaction, as an important methodology, has been utilized to construct complex product from ordinary starting materials. In this report, many typical organoamine catalysts were investigated to achieve highly efficient asymmetric three-component reaction of enones 2, aldehydes 3 and Meldrum’s acid 4. Various pharmacological multi-substituted spiro[5,5]undecane-1,5,9-triones promoted by 9-amino-9-deoxy-epi-quinine 1 g in one-pot, were obtained in moderate to good yields (up to 81%) with excellent diastereo-(>99:1 dr) and enantioselectivities (up to 97% ee). Meanwhile, based on the controlled experiments and analytical data, a reasonable mechanism of dual-activity for this reaction has been proposed.     

Synthesis and photoresponsive behavior of azobenzene‐containing side‐chain liquid crystalline diblock polymers with polypeptide block

Well‐defined azobenzene‐containing side‐chain liquid crystalline diblock copolymers composed of poly[6‐(4‐methoxy‐azobenzene‐4′‐oxy) hexyl methacrylate] (PMMAZO) and poly(γ‐benzyl‐L ‐glutamate) (PBLG) were synthesized by click reaction from alkyne‐ and azide‐functionalized homopolymers. The alkyne‐terminated PMMAZO homopolymers were synthesized by copper‐mediated atom transfer radical polymerization with a bromine‐containing alkyne bifunctional initiator, and the azido‐terminated PBLG homopolymers were synthesized by ring‐opening polymerization of γ‐benzyl‐L ‐glutamate‐N‐carboxyanhydride in DMF at room temperature using an amine‐containing azide initiator. The thermotropic phase behavior of PMMAZO‐b‐PBLG diblock copolymers in bulk were investigated using differential scanning calorimetry and polarized light microscopy. The PMMAZO‐b‐PBLG diblock copolymers exhibited a smectic phase and a nematic phase when the weight fraction of PMMAZO block was more than 50%. Photoisomerization behavior of PMMAZO‐b‐PBLG diblock copolymers and the corresponding PMMAZO homopolymers in solid film and in solution were investigated using UV–vis. In solution, trans–cis isomerization of diblock copolymers was slower than that of the corresponding PMMAZO homopolymers. These results may provide guidelines for the design of effective photoresponsive anisotropic materials. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

生长素自旋标记物的合成及生物活性

将４－氧－２，２，６，６－四甲基哌啶－１－氧自由基（ＴＭＰＯ）与３种植物生长素拼接在一起，合成了相应的腙，以研究ＴＭＰＯ对生长素活性的影响．所得化合物的结构通过ＩＲ、ＥＳＲ、元素分析或ＭＳ加以证实．初步生物活性测定表明，与母体相比不仅对绿豆幼苗的生长促进作用无影响，在一定条件下还增强了促进生长的活性