Study on the Range of Particles Size Measured by Backscattering Method in Visual‐infrared Incident Spectrum

For the measurement of particles size with backscattering method, the suitable range of particles size measurement have been presented by independent algorithm in Visual‐infrared incident spectrum. We defined the range according to the retrieved results based on the analysis and comparison to many kinds of R‐R distribution function. The simulation computation results showed that the particles size measurement range is from 0.05 μm to 18 μm with incident spectrum from 0.4 μm to 2 μm and different refractive index. The results retrieved were satisfied even if 1 % noise was added into the backscattering intensity.     

Exact field-driven interface dynamics in the two-dimensional stochastic Ising model with helicoidal boundary conditions

We investigate the interface dynamics of the two-dimensional stochastic Ising model in an external field under helicoidal boundary conditions. At sufficiently low temperatures and fields, the dynamics of the interface is described by an exactly solvable high-spin asymmetric quantum Hamiltonian that is the infinitesimal generator of the zero range process. Generally, the critical dynamics of the interface fluctuations is in the Kardar–Parisi–Zhang universality class of critical behavior. We remark that a whole family of RSOS interface models similar to the Ising interface model investigated here can be described by exactly solvable restricted high-spin quantum XXZ$XXZ$-type Hamiltonians.     

小型荧光激光雷达测量六种典型生物战剂模拟物二维荧光光谱

对成团泛菌(Pan)、金黄色葡萄球菌金黄亚种(Sta)、球芽孢杆菌(BG)和大肠杆菌(EH)四种生物战剂模拟物进行了培养和生长曲线测定,四种菌的代时分别为0.99,0.835,1.07和1.909 h;设计研制了近场小型荧光测量激光雷达,266和355 nm波长分别用于测量生物战剂模拟物氨基酸段和NADH段二维荧光谱;在可控的荧光测量腔室,测得了分辨率为4 nm的营养态细菌液态气溶胶以及牛血清(BSA)、卵清蛋白(OVA)两种毒素类模拟物液态气溶胶的二维荧光谱;二维荧光谱数据表明,Pan,Sta,BG,EH,BSA和OVA气溶胶,在氨基酸段的荧光谱形与标准荧光组分色氨酸较为一致,FWHM为60 nm,受培养生化环境、细菌内部荧光组分及比例的影响,荧光分子激发态与基态间的能量差增大,荧光谱带均存在不同程度的蓝/紫移;在Pan,Sta,BG和EH营养细菌气溶胶中均检出了较弱的NADH荧光组分,且水、氮等的拉曼散射不能完全扣除,光谱锯齿严重,FWHM为100 nm;二阶求导后的二维荧光谱表明,荧光谱的高阶处理和分辨识别是可行的。     

无穷维Hamilton算子的二次数值域

研究了一类无界无穷维Hamilton算子的二次数值域的性质,进而,应用二次数值域来刻画了无穷维Hamilton算子谱的分布范围,并给出了二次数值域的闭包包含谱集的结论.     

正交光楔激光远场焦斑测量方法

为验证正交光楔激光远场焦斑测量方法在提取光斑高频组分、扩展CCD测量动态范围和减小光束质量测量误差等诸方面的有效性,以常用的光束质量因子作为衡量新方法有效性的指标,建立离焦光斑强度分布理论模型并搭建相应的实验平台进行实验验证。验证结果表明:新方法与传统远场测量方案相比,使实验所用CCD的测量动态范围拓展了约9倍,实际光斑远离中心主核区域的大量高频旁瓣分布特征从CCD背景噪声起伏中凸显出来,光束质量因子的测量平均相对误差也有约16%的精度改善。     

两个投影算子的组合的幂等性

研究了两个交换的投影算子P和Q的组合aP+bQ+cPQ(a≠0,b≠0)的幂等性,并给出了它们的值域与核.利用矩阵的CS-分解研究了两个正交投影算子P和Q的组合aP+bQ+cPQ(a≠0,b≠0)的正交幂等性,证明了只有当两个正交投影算子P与Q交换时,aP+bQ+cPQ才有可能是正交幂等的.这些结果刻画了两个投影算子的一些重要特性.     

统计质量保证技术在分析测试实验室内部质量控制中的应用

对通过统计质量保证（SQA）技术进行分析测试实验室内部质量控制（IQC）的方法作了初探。研究结果表明,SQA技术的应用能保证实验室始终处于统计受控状态,确保测试数据的有效性,有利于分析测试实验室质量保证活动的开展。     

多糖凝胶的孔径和化学结构对单壁碳纳米管流动性和选择性分离的影响

基于凝胶柱色谱分离技术研究了单分散的单壁碳纳米管（SWCNTs）在不同化学结构多孔多糖凝胶中的流动特性以及对金属型（m-）/半导体型（s-）SWCNTs 分离的影响. 通过比较SWCNTs 在一系列不同孔径的葡聚糖Sephacryl 凝胶中的流动行为,发现减小孔径尺寸能够增强s-SWCNTs 与凝胶之间的吸附作用力,使大直径的m-SWCNTs 快速地流过凝胶颗粒,而选择性地保留了小直径的s-SWCNTs. 进一步发现多糖凝胶化学结构比孔径尺寸在SWCNTs 的m/s 分离中起着更重要的作用. 当基于葡聚糖结构的Sephacryl 凝胶中的氨基结构被琼脂糖结构所取代时,如Superdex 200 和Sepharose 2B凝胶会增强它们与SWCNTs 之间的作用力,使SWCNTs 的保留时间延长,降低了s-SWCNTs 的选择性和纯度. 此外,即使拥有与Sephacryl S100类似的孔径范围,当Sephacryl 凝胶中的氨基被疏水环氧丙烷基团取代时,葡聚糖凝胶Sephadex G100 与SWCNTs 的作用力很弱,导致所有SWCNTs 快速流动,无法实现SWCNTs 的m/s 分离. 因而,我们认为凝胶孔径和化学结构共同影响并调控了SWCNTs的m/s分离的选择性、纯度以及分离效率.     

Observation of latent tracks formed by heavy ion irradiation in poly(methyl methacrylate)

The irradiation effect in poly(methyl methacrylate) changed from main‐chain scission to crosslinking, depending on the stopping powers of the Au and Xe ions irradiated with high stopping powers. The latent ion tracks, including an end of the ion range in the polymer, were observed clearly by field emission and atomic force microscopies. Additionally, it was also observed that a crosslinked structure (formed by nuclear stopping) existed across an end of the ion range calculated by a Transport of Ion in Matters code, and it was different from that formed by electronic stopping. The nuclear stopping of the heavy ions can play an important role around the end of the ion range in the polymer. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 757–762, 2001