碳纤维用PAN原丝超声波水洗新技术

为降低PAN原丝中的DMSO(二甲基亚砜)残留量,减少其对原丝的拉伸、预氧化处理等过程的不利影响而造成的碳纤维的结构缺陷、强度降低,将超声波水洗技术应用到PAN原丝水洗工艺中.结果证明,新方法明显提高了水洗效果,能够快速有效地降低原丝中DMSO残留量.     

基于DCT-CS的脉冲星周期超快速估计方法

受快速傅里叶变换（fast Fourier transform，FFT）的影响，基于FFT和压缩感知（compressive sensing, CS）的脉冲星周期快速估计算法的计算量大。为进一步减小计算量并提高计算精度，利用离散余弦变换（discrete cosine transform，DCT)取代FFT，提出了一种基于DCT-CS的脉冲星周期超快速估计算法。在该方法中，利用DCT提取脉冲星信号的低频部分构建低频DCT矩阵；构建畸变轮廓字典并获取累积轮廓；提出了利用最大值超分辨率稀疏恢复估计脉冲星周期的方法。仿真结果表明，DCT-CS的脉冲星周期估计精度达到了3.82×10-12 s，计算时间达到了9.31 ms。与FFT-CS相比，周期估计精度提高了约16%，计算时间缩短了约37.5%，实现了实时高精度的脉冲星周期估计。     

高雷诺数槽道湍流的壁面模化大涡模拟研究

选取基准壁湍流的槽道流动,研究了多种模型的壁面模化大涡模拟.模型包括经典的大涡模拟、Spalart-Allmaras、分离涡模拟和一种动态混合模型.基于摩擦速度的雷诺数范围为395~12000,采用3组粗糙网格,流向和展向维数分别同取37,49和65,法向维数保证y+(1)~1.主要研究平均速度、雷诺切应力分布、详细分析了各模型的特性差异并展示了相应的湍流结构.研究表明:在高雷诺数粗糙网格下,大涡模拟失去求解精度,分离涡模拟出现对数律不匹配,动态混合模型的计算接近直接数值模拟,其对数率区可解应力约占雷诺切应力的93%,边界层外层可解应力约占99%.这说明合适的混合模型可以在经济成本下保证计算精度,具有解决实际问题的潜力.      

软件可靠性测试数据生成方法研究

阐述了构造非实时软件运行剖面的方法,以及根据运行剖面生成非实时软件可靠性测试数据的方法,并提出了构造实时软件运行剖面和生成实时软件可靠性测试数据的思路。最后给出实例,系统地演示非实时软件可靠性测试数据的生成过程。     

基于复合疲劳试验的涡轮叶片振动应力反推法

提出了一种利用复合疲劳试验和外场故障数据反推涡轮叶片实际振动应力的方法.该方法针对与故障叶片同批次的叶片,开展数个振动应力水平下的单件试验和某一特定振动应力水平下的成组试验,利用极大似然法推导出叶片的概率-应力-寿命曲线(P-S-N);最后基于99.87%存活率下的概率-应力-寿命曲(P_99.87%-S-N),结合叶片的外场故障统计结果,反推出叶片实际工作中振动应力的范围和可能的最大振动应力.      

基于频域分析的ROSAR成像算法

在现有的ROSAR(Synthetic Aperture Radar with Rotating antennas)成像算法中,基于斜距泰勒级数展开的算法存在方位向失配问题,时域相关卷积算法不能快速校正距离弯曲.频域ROSAR成像算法采用驻相点原理,直接对ROSAR回波信号进行二维频域变换,保留回波信号的频谱特征,进而构造相应的频域去耦函数和频域匹配函数,实现频域距离弯曲校正和目标场景重构.仿真结果表明,该算法能够快速校正距离弯曲及有效克服方位向失配问题.     

基于开源GIS数据的广域小重叠卫星影像定位模型精化

设计了一种适用于大区域、小重叠卫星影像有理多项式模型(RPC)定位精度优化的技术流程,基于开源数字正射影像(DOM)、数字高程模型(DEM)数据和RPC几何模型约束,通过优化尺度不变特征变换(SIFT)特征提取与匹配算法,实现了无像幅约束的控制点和连接点的快速稳健匹配,应用DEM支持下的RPC模型二维区域网方法实现了多景影像RPC模型精度的联合精化。GF-1卫星WFV影像的实验结果表明:在DEM支持下经过区域网平差后,RPC模型的定位精度可达到像素级水平。     

Investigation on Thermal and Dimensional Stability of Epoxy Resin In-Situ Modified by Cyanate Ester Resin and Polydimethylsiloxane

The thermal and dimensional stability of epoxy resin (EP) in-situ modified by cyanate ester (CE) and polydimethylsiloxane (PDMS) are investigated by means of experiments and numerical simulation. Thermal gravimetric analysis (TGA) and differential scanning calorimeter (DSC) are used to analyze the heat resistance of the modified EP. The dimensional stability is characterized by the volume shrinkage of the series PDMS/CE/EP obtained by the density method. The chemical structure of the PDMS/CE/EP is analyzed by Fourier transform infrared spectroscopy (FTIR). The results of TGA and DSC indicate that the thermal stability of PDMS/CE/EP decreases firstly and then increases with the increase in the amount of CE. The addition of PDMS shows a slight effect on the thermal stability. The 40% CE makes the blending system exhibit the lowest initial decomposition temperature, which reduces by 15.5% and 40.8% compared with pure EP and CE, respectively. The FTIR results suggested that the influence of CE on the thermal stability of the modified EP is mainly ascribed to the generation of oxazolidinone ring with low thermal stability and the increase in the triazine ring with high thermal stability. The volume shrinkage measurement results show that the introduction of CE and PDMS are both beneficial to the improvement of the dimensional stability of the blending systems. The in-situ addition of 80% CE shows the lowest volume shrinkage of 6.11%. The thermal stress distribution of PDMS/CE/EP generated during the solidification process is simulated by the finite element analysis. The results suggested that the introduction of 80% CE into EP results in the lowest thermal stress in the blending system, which indicates that the system has the lowest volume shrinkage, which agrees well with the experimental results.