导弹发射姿态测量方法研究

针对导弹发射姿态测量问题,提出采用高速摄像机通过斜瞄和平瞄姿态测量方法求解导弹中轴线俯仰角和方位角,仿真典型导弹起飞段近距离姿态测量,分析两种测量方法对导弹飞行姿态测量精度和适用性。仿真结果表明:平瞄和斜瞄姿态测量方法,测量误差在0.2°以内。斜瞄方式使用更便捷,通用性好。平瞄方式测量精度高,数据处理方法、机械结构相对简单,在适合的应用场合优势明显。此分析方法、分析结果为姿态测量方法选取和研究等提供一种可行的途径,也可为其它运动目标的姿态测量提供借鉴。     

空空导弹测试系统应用LXI总线研究

首先对空空导弹测试系统应用各种仪器总线的情况进行了分析研究,然后介绍了一台PXI总线测试设备的改造方案,该方案中设计了一套基于LXI总线控制的电源子系统,该子系统与PXI主系统一起形成了新的混合总线控制测试设备。该改造方案实现了改造需求中的低成本和小型化设计。同时,结合该方案分析了LXI总线在空空导弹测试系统上应用的优缺点和现阶段局限性。提出了空空导弹测试系统应向着通用、开放和网络化方向发展的观点,得出了未来的空空导弹测试系统将是包含GPIB、VXI、PXI、LXI等总线接口的合成系统,各总线接口仅是网络上的一个节点的结论。     

高温超导电缆直流测试电源平台的搭建

根据高温超导电缆测试用直流电源平台的要求,建立了硬件平台。该平台为模块化结构,具有输出精度高,便于扩展等特点;为方便操作,建立了基于LabVIEW的软件平台,对直流电源平台进行远程控制,并给出了远程控制的程序流程图,实现了电流的匀速上升和下降以及上升过程中的中断操作;利用该电源平台进行了超导电缆的临界电流测试实验,验证了直流电源平台符合高温超导电缆的测试要求。     

机载光电平台目标定位与误差分析

根据机载光电平台的特点,建立了6个坐标系统,进行了8次线性变换,构建了从光电平台成像系统像面坐标系到大地地理坐标系的目标定位数学模型。计算了目标在大地地理坐标系的经纬度和高程坐标,分析了各种测量参数对目标定位精度的影响。通过建立误差模型和仿真数据进行目标定位实验,采用蒙特卡罗方法统计目标定位误差。实验结果表明,载机经纬度误差、载机姿态角度误差及光电平台指向角度误差是影响目标定位精度的主要因素,其中载机经纬度误差直接传递到目标定位误差,载机姿态角度误差和光电平台指向角度误差大体上以10-4～10-2比例作用到目标定位误差。本文方法有效可行,对机载光电平台目标定位具有实用价值。     

大学物理实验课程建设的研究与实践

结合课程建设的实践,阐述了吉林大学大学物理实验分层次教学的课程体系,“层次化、自主化、研究化”的教学理念,教学团队的建设思路.构建本科生公共物理创新实践平台的实施措施及所取得的成效,介绍了网络教学与管理平台的构架及课程未来的建设目标.     

高能e+e－湮没强子多重数的质量关系

利用一个描述强子质量谱成功的夸克模型确定出得到的强子多重数普适质量关系〈n〉=aexp(–bm)中的参数b,发现对于介子、重子是一个普适的常数.利用这个质量公式给出计算各种粒子多重数的表达式,进而以高能e⁺e^－湮没为例计算出各种粒子多重数与实验以及其他模型做了比较,表明这个没有任何假定的质量关系同样能够解释实验.     

Convergent Star Product Algebras on ‘ax+b’

We define nontempered (exponential growth) function spaces on the Lie group ax+b which are stable under some left-invariant (convergent) star product. The techniques used to achieved the latter come from symmetric spaces geometry and star representation theory.     

Our trails and trials in the subsarcolemmal cytoskeleton network and muscular dystrophy researches in the dystrophin era

In 1987, about 150 years after the discovery of Duchenne muscular dystrophy (DMD), its responsible gene, the dystrophin gene, was cloned by Kunkel. This was a new substance. During these 20 odd years after the cloning, our understanding on dystrophin as a component of the subsarcolemmal cytoskeleton networks and on the pathomechanisms of and experimental therapeutics for DMD has been greatly enhanced. During this paradigm change, I was fortunately able to work as an active researcher on its frontiers for 12 years. After we discovered that dystrophin is located on the cell membrane in 1988, we studied the architecture of dystrophin and dystrophin-associated proteins (DAPs) complex in order to investigate the function of dystrophin and pathomechanism of DMD. During the conduct of these studies, we came to consider that the dystrophin-DAP complex serves to transmembranously connect the subsarcolemmal cytoskeleton networks and basal lamina to protect the lipid bilayer. It then became our working hypothesis that injury of the lipid bilayer upon muscle contraction is the cause of DMD. During this process, we predicted that subunits of the sarcoglycan (SG) complex are responsible for respective types of DMD-like muscular dystrophy with autosomal recessive inheritance. Our prediction was confirmed to be true by many researchers including ourselves. In this review, I will try to explain what we observed and how we considered concerning the architecture and function of the dystrophin-DAP complex, and the pathomechanisms of DMD and related muscular dystrophies.     

大学物理演示实验网络教学管理平台构建与实施

详细介绍了我校开发的“大学物理演示实验网络教学管理平台”的框架,其在教学管理中所发挥的作用,运行的效果,特别是在低年级本科生创新能力培养中所显现的效果.     

Enhanced renal image contrast by ethanol fixation in phase‐contrast X‐ray computed tomography

Phase‐contrast X‐ray imaging using a crystal X‐ray interferometer can depict the fine structures of biological objects without the use of a contrast agent. To obtain higher image contrast, fixation techniques have been examined with 100% ethanol and the commonly used 10% formalin, since ethanol causes increased density differences against background due to its physical properties and greater dehydration of soft tissue. Histological comparison was also performed. A phase‐contrast X‐ray system was used, fitted with a two‐crystal X‐ray interferometer at 35 keV X‐ray energy. Fine structures, including cortex, tubules in the medulla, and the vessels of ethanol‐fixed kidney could be visualized more clearly than that of formalin‐fixed tissues. In the optical microscopic images, shrinkage of soft tissue and decreased luminal space were observed in ethanol‐fixed kidney; and this change was significantly shown in the cortex and outer stripe of the outer medulla. The ethanol fixation technique enhances image contrast by approximately 2.7–3.2 times in the cortex and the outer stripe of the outer medulla; the effect of shrinkage and the physical effect of ethanol cause an increment of approximately 78% and 22%, respectively. Thus, the ethanol‐fixation technique enables the image contrast to be enhanced in phase‐contrast X‐ray imaging.