井间地震反射波资料处理

井间地震反射波资料处理可以看成是有偏VSP反射波资料处理的一种延伸。由于一对井间地震资料相当于近千个有偏VSP，加上反射角增大和频率大幅度提高（约10倍），因此，井间地震反射波资料处理有着自身的一些特点。为此，对井问地震反射波资料处理中的一些技术和问题进行了讨论。对井间地震资料进行了分析，指出井间地震资料具有反射波场较弱、频率很高、管道波能量很强等特点；介绍了井间地震资料预处理方法，从空间属性建立、数据选排（抽道集）、道编辑、频谱分析、随机噪声压制和管波等相干噪声压制诸方面进行了讨论；对井间地震资料的波场分离和成像中需要注意的几个关键性问题进行了探讨，对于井间地震资料的高频特性给噪声压制和同相叠加处理造成的困难，通过提高叠加次数予以解决，对于大反射角对同相叠加造成的影响，则采用限角叠加技术来解决。实际资料处理表明，所采用的处理技术和措施合理有效，获得的反射波剖面品质良好。     

单片LCoS光学引擎中彩色LED照明系统设计

LCoS光学引擎作为整个背投的一个要组成部分，其照明系统显著地影响着LCoS背投的性能。详细分析了影响照明效果的各个因素，并利用ZEMAX软件设计出了单片LCoS光学引擎中基于彩色LED光源的照明系统，该系统能达到较好的亮度和均匀性，满足整个光机系统的成像要求。     

新型微光探测器激光防护材料的研究

系统分析了微光夜视器的结构及其原理，并结合当前器件存在的激光致盲威胁，提出了增强系统安全的新措施。同时，系统地介绍了防激光滤光材料一些重要的性能参数以及滤光材料的组成、制备加工工艺。研究结果表明，新型的防激光材料能够有效地防护800nm，900nm以及10613nm等三个波长的激光，并且可见光透过率大于85％。     

测量光纤放大器小信号增益谱的一种简便方法

提出了一种用小功率宽带光源较精确测量光纤放大器小信号增益谱的方法。数值模拟表明 ,该方法是完全可行的 ,并且实验结果与数值模拟结果一致。该方法具有简便、易操作的特点。     

入射光的偏振和强度对分光镜透／反比的影响

采用能量流分析法推导了一束线偏振光经分光镜分光形成透射／反射光的能量表达式。分别讨论了入射光强度不变而偏振方向变化以及二者同时变化对分光镜透／反比的影响。通过旋转主光路中的偏振片来模拟入射光的偏振方向和强度变化，实验验证了分光比的变化规律。     

低光照和抗晕CCD的设计和制作

针对帧转移可见光CCD低光照响应、抗电晕能力和动态范围，较详细讨论了CCD光响应灵敏度、动态范围和抗电晕的设计与计算。设计的具有抗晕功能CCD，采用2μm工艺制作，达到了设计技术指标要求，满足了工程应用需求。     

声光效应拉曼-内斯方程矩阵级数解法及声光调制器优化设计

提出一种求解正常声光相互作用拉曼 内斯 (Raman Nath)方程的矩阵级数解法 ,该解法直观方便且具有普遍性。计算结果表明 ,对Q =4 1π ,Bragg衍射的效率只有 97 5 % ;对非对称入射 ,以往的Raman Nath近似解误差较大 ;指出提高Bragg衍射效率的有效途径在于提高声光频率比并给出计算声光器件最优长度的计算公式。     

强度反射型光纤温度传感器

本文提出并研究了一种新型的强度反射型光纤温度传感器.根据定容气体温度与压力的线性关系,通过简单的测温元调制光纤中的反射光强,从而得知待测温度.这种传感器结构紧凑,造价低廉.在30~50℃范围内,灵敏度可以达到30mV/℃以上.     

Unperturbed dimension of poly(4-acetoxystyrene) measured in good and theta solvents

In order to obtain the additional data concerning the unperturbed dimension of poly-4-substituted styrene, light scattering measurements are performed on the twenty-two fractions with molecular weight of (0.91–352)·10⁴ of poly(4-acetoxystyrene) in dioxan at 25°C, from which the molecular weight obtained was found easily to be evaluated with the gel permeation chromatography using THF. Phase separation experiments for this polymer indicate that the theta state is attained in isopropyl acetate at 19.7°C and butyl acetate at 26.8°C. By making viscosity measurements at that state, the value of K_Θ is directly evaluated as 5.4·10^?4 dl g^?1. The limiting viscosity number is also obtained in good solvents, THF and dioxan, at 25°C and constants of the Mark-Houwink-Sakurada equation in each solvent are determined. Further, approximately the same K_Θ as above is obtained from these data with the Stockmayer-Fixman plot. The calculated value of steric factor, 2.37, on this polymer may be plausible, compared with those of polyvinylaromatic derivatives.     

Critical-point drying versus freeze drying for scanning electron microscopy: a quantitative and qualitative study on isolated hepatocytes

Critical-point drying and freeze drying were compared both quantitatively and qualitatively as preparative procedures for scanning electron microscopy. Isolated hepatocytes were used as model cells. Nomarski differential interference contrast microscopy was used for light microscopic measurements of the hepatocytes in the unfixed, the glutaraldehyde fixed, the glutaraldehyde + OsO₄ fixed, the critical-point dried and the freeze dried states. Critical-point dried hepatocytes were found to shrink to 38% of glutaraldehyde + OsO₄ fixed volume, whereas optimal freeze dried hepatocytes (frozen in water saturated with chloroform and freeze dried at 183 K for 84 h) were found to shrink to 51% of glutaraldehyde + OsO₄ fixed volume. Transmission and scanning electron micrographs of the critical-point dried cells showed well-preserved ultrastructure and surface structure. Micrographs of the freeze dried cells showed ultrastructure destroyed by internal ice crystals and surface structure destroyed by external ice crystals. Double-fixed isolated hepatocytes were shown to swell during storage in buffer and to shrink during storage after critical-point drying. For low magnification scanning electron microscopy (up to about 3000 times) both critical-point drying and freeze drying can be used. However, for high magnification scanning electron microscopy, critical-point drying is superior to freeze drying.