Al_2O_3微孔膜对60keV O~+离子的“导向”效应

在不同入射角度条件下,研究了60keV的O+离子入射孔径分别为50nm和30nm,厚度为10μmAl2O3微孔膜的角分布.实验结果表明离子透射微孔膜时发生了导向效应,随着入射角度的增大,透射于孔径大的微孔膜离子计数下降比较快,透射于孔径小的微孔膜离子计数下降比较缓慢.建立了一个初步的理论模型,对以上现象给出了较好的解释.     

低能高电荷态离子(4≤q≤7)与He碰撞中双俘获与转移电离的截面反转效应

基于入射离子双俘获后势能沉积与双电离靶离子势能的比值定义了势能参数Ω,研究了低能高电荷态离子(q=4,5,6,7)与He原子碰撞系统中双俘获和转移电离反应道的选择规律.研究发现,在Ω坐标下,双俘获和转移电离存在截面反转效应,Ω1.0时双俘获为双电子转移过程主反应道,Ω≥1.0时转移电离成为双电子转移过程主反应道.     

高电荷态Ar~(17+)离子在表面以下过程中发射X射线分支比及各分支能量的研究

对低速高电荷态Ar17+离子在与不同金属靶相互作用过程中放出的Ar离子K壳X射线的Kβ/Kα分支比及各分支K线平均能量进行了理论研究.在文献[28,29]的基础上,通过对实验数据的分析,得到了0.3—0.8玻尔速度之间的Ar17+离子与Be,Al,Ni,Mo,Au等金属相互作用过程中入射离子发出的X射线分支比及各分支平均能量.理论上,基于导带电子俘获模型和级联跃迁模型,建立耦合方程组,以解释实验主要结果,理论结果与实验符合较好.在此基础上讨论了低速高电荷态Ar17+离子在金属表面以下的空心原子形成及退激发过程中发射K壳X射线的物理图像.     

低功率氩电弧加热发动机的数值模拟

采用可求解可压缩流动与传热的全速度SIMPLE算法,对低功率氩电弧加热发动机内部的传热与流动进行了数值模拟,获得了电弧加热发动机内的温度、速度、马赫数及流线分布。计算结果表明:电弧加热发动机内最高温度出现在阴极下游附近中心轴线处,这是因为电弧在阴极表面收缩形成阴极弧点,从而焦耳热成为该高温区的主要加热机制;沿着发动机中心轴线,气体温度和速度开始时随着距阴极距离的增加而迅速增加,然后在等离子体流向喷管出口的过程中,气体温度和速度逐渐下降。此外还详细考察了弧电流变化对电弧加热发动机内部传热与流动特性的影响,计算获得的发动机流量和比冲与实验结果基本一致。     

强扰动能区非全裸Cq+,Oq+(q=1-4)与He原子碰撞过程中截面比的实验研究

利用兰州大学2×1.7MV串列加速器离子-原子碰撞实验终端上产生的单核子能量为20-500 keV的Cq+和Oq+(q=1-4)离子与He原子碰撞.采用符合测量方法和多参数数据获取系统得到了散射离子与反冲离子电荷态的二维谱,从而分别得到直接电离、入射离子俘获电子和入射离子损失电子截面与总截面的截面比Rdirect,Rcapture和Rloss,并对强扰动能区的各个反应道之间竞争关系及同一反应道在不同碰撞体系中所表现出的实验规律进行了比较和定性分析.     

Studies of K-shell x-ray energy shifts induced by MeV/u heavy ions

This paper reports that the K x-ray spectra of the thin target 47Ag, 48Cd, 49In and 50Sn were measured by an HPGe semi-conductor detector in collisions with 84.5 MeV 6C4+ ions. Our experiment revealed the Kα x-ray energy shifts were not obvious and the Kβ1 x-ray energy shifts were about 90～110 eV. The simple model of Burch et al has been previously used to calculate the K x-ray energy shifts due to an additional vacancy in 2p orbit. The present work extends the model of Burch to calculate the x-ray energy shifts of multiple ionized atoms induced by heavy ions with kinetic energy of MeV/u. In addition to our experimental results, many other experimental results are compared with the calculated values by using the model.     

中低速C3+与He,Ne,Ar原子相互作用过程中单电子转移绝对截面的测量

实验测量了1.7v0-4.2v0(v0为玻尔速度,v0=2.19×108 cm/s)的C3+与He,Ne,Ar原子碰撞过程中单电子转移绝对截面.将实验结果与多体经典轨道蒙特卡罗模拟计算结果做了比较,发现测量结果与多体经典轨道蒙特卡罗模拟计算结果在趋势上相符.当入射离子速度在1.7v0-2.0v0时,因多体经典轨道蒙特卡罗方法计算时不能考虑多电子关联态俘获和极化效应的影响,实验值大于计算值.当入射离子速度在2.2v0-4.2v0时,由于被俘获电子对入射离子的不完全屏蔽,加上电子间的动态关联及有效电荷的影响,实验结果先与多体经典轨道蒙特卡罗计算结果符合很好,而后逐渐大于计算值.此外,还根据转移电离与单电子俘获的截面比简单分析了转移电离机制.     

30 keV H+在聚碳酸酯微孔膜中动态输运过程的实验和理论研究

测量了30 keV的H⁺入射倾斜角度为-1°和-2°的聚碳酸酯微孔膜后,出射粒子二维分布图、角度分布、相对穿透率以及出射H⁺电荷态纯度随沉积电荷的演化.实验中30 keV的H⁺在微孔膜中输运特性与之前其他能区离子在微孔膜中输运特性有显著不同,实验中直接观测到出射粒子导向部分和散射部分的动态演化过程,出射的H⁺由沿微孔孔轴方向的导向H⁺和沿入射束流方向的散射H⁺两部分组成,随着微孔内电荷斑的沉积,出射的导向H⁺的占比不断减小,出射散射H⁺占比不断增加;出射H⁰占总出射粒子的比例不断减小,其中心方向逐步向入射束流方向偏转.微孔膜处于不同倾斜角度时,微孔内沉积电荷斑的位置和电场强度是不同的.同时模拟计算了入射H⁺在微孔内部的运动轨迹、微孔内部电荷斑电势和场强分布,实验结果和理论结果得到了很好的验证.对出射离子导向部分和散射部分的动态演化过程的观测和理论解释,使得对中能区离子在微孔膜中输运机制有更好的认识.     

Investigation of transfer ionization in collisions of partially stripped carbon ions with helium at low to intermediate velocities

The ratios of transfer ionization (TI) to single-electron capture (SC) cross sections have been measured for the collisions of partially stripped C^q+ ions (q=1--4) with He. The collision velocity ranges from 0.7 to 4.4v₀ (v₀ is the Bohr velocity). The projectile-ion and recoil-ion coincidence technique is used to separate the processes of TI and SC. The ratios reach the maximum when the velocity is about 3.7v₀ This can be explained qualitatively based on the two-step mechanism. The experimental results are also compared with the results calculated using the classical trajectory Monte Carlo (CTMC) method. The CTMC results are in agreement with the experimental data basically. The discrepancies in higher velocity region are interpreted by the effective charge effect.     

Crystal Structure and Bovine Serum Albumin Binding Studies of Methyl 4-(2,4-Dichlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

The title compound, methyl 4-(2,4-dichlorophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate(C_(20) H_(21)Cl_2NO_3, 1) was synthesized and the crystal structure was —determined by single-crystal X-ray diffraction. It crystallizes in tetragonal system, space group P421 c with a = 16.076(3), b = 16.076(3), c = 14.750(2) ?, V = 3811.8(14) ?3, Z = 8, R = 0.0377 and wR = 0.0845. The interactions between compound 1 and bovine serum albumin(BSA) were investigated using fluorescence spectroscopy. The results revealed that compound 1 can effectively quench the intrinsic fluorescence of BSA by static quenching mechanism. The thermodynamic parameters revealed that the action forces between compound 1 and BSA were mainly van der Waals forces and hydrogen bonds. According to F?rster's non-radioactive energy transfer theory, the binding distance between compound 1 and BSA had been determined. Furthermore, the synchronous fluorescence showed that compound 1 has few effects on the microenvironment and conformation of BSA in the binding process.