基于弹性波散射对二维障碍物边界的识别

给出了二维障碍物弹性波散射场的一种近似积分形式 ,基于 Fourier变换法建立了均匀障碍物特征函数与其远场散射振幅中形状因子的关系式 ,最后就基体为锌 ,对圆形和椭圆形截面铁夹杂进行了计算机模拟 ,结果表明该反演方法对定量无损检测技术具有应用价值。     

Latest results from HERA

Highlights are presented of the latest measurements from the H1, ZEUS and HERMES experiments at HERA.     

共振光散射法测定丁胺卡那霉素

研究了以达旦黄（TY）作为共振光散射探针测定市售药品中丁胺卡那霉素（AMK）的测定方法．该方法基于在pH=5．5的Britton—Robinson缓冲溶液中，达旦黄和丁胺卡那霉素结合后有强烈的共振光散射作用．在λ=482nm处，共振光散射强度（△IRLS）最大且光散射的强度与AMK的浓度在0．4～2．4mg·L^-1范围内成正比（相关系数r=0．9986），检出限为8．6×10^-3mg·L^-1．该方法简便、快速、灵敏，对1．0mg·L^-1的AMK溶液平行测定11次，RSD=2．57％．用于市售样品的分析测定，结果满意。     

Surface structure of low-coveraged Cs on Si(0 0 1)-() system

Alkali metals (AM) on semiconductors have been investigated as a simple model system for the metal-semiconductor interfaces due to their simple electronic structures. Especially, cesium (Cs) on Si(0 0 1) surface has been studied with various experimental techniques. In this study, we investigated the atomic structure of initial Cs adsorption on Si(0 0 1)-(2×1) surface using coaxial impact collision ion scattering spectroscopy. When Cs atoms are adsorbed on Si(0 0 1)-(2×1) up to 0.2 ML at room temperature, the initial adsorption site is on-top T3 site with poor periodicity and the length of Si dimer is reserved as in the clean Si(0 0 1) surface. It is also found that Cs atoms adsorbed on Si(0 0 1) surface with a height of 2.83±0.05 Å from the second layer of Si(0 0 1) surface.     

Significance of absolute energy scale for physics at BESⅢ

The effects of absolute energy calibration on BESⅢ physics are discussed in detail,which mainly involve the effects on τ mass measurement,cross section scan measurement,and generic error determination in other measurements.     

Non-existence of stationary two-black-hole configurations

We resume former discussions of the question, whether the spin–spin repulsion and the gravitational attraction of two aligned black holes can balance each other. To answer the question we formulate a boundary value problem for two separate (Killing-) horizons and apply the inverse (scattering) method to solve it. Making use of results of Manko, Ruiz and Sanabria-Gómez and a novel black hole criterion, we prove the non-existence of the equilibrium situation in question.     

A Simple X-ray Spectrometer and PC-based Data Acquisition System for Newly Developed X-ray Source Based on Laser Compton Scattering

A simple X-ray spectrometer and a PC-Based Data Acquisition System(DAS) have been developed newly in Shanghai Institute of Applied Physics(SINAP),Chinese Academy of Sciences (CAS) for the measurement of the X-ray source generated using laser Compton scattering.The system consists of liquid nitrogen cooled high resolution Si(Li) detector,electronics and a DAQ.The Si(Li) detector was designed and made by Center of Advanced Instruments in SINAP,CAS,it allows us to measure X-rays with the energy up to 60 keV and the energy resolution(FWHM) of 184 eV at 5.9 keV.We measured the system uncertainty was 0.2 eV and time drifting of detector was 0.05% both at 5.9 keV.The DAQ was based on Object-Oriented software LabVIEW 7.1,it has data on-line analysis and original data saved functions.     

Inelastic neutron scattering from isotactic polypropylene

We used inelastic neutron scattering to probe the low‐energy excitations in semicrystalline isotactic polypropylenes with different degrees of crystallinity. The contributions from the amorphous and crystalline regions to the total scattering intensity were extracted under the assumption of a weighted linear contribution of the two regions in a simplified two‐phase system. The resulting intensity from the amorphous region showed a peak at 1.2 meV that was in good agreement with the previously determined boson peak characteristic of atactic polypropylene. The possibility of a contribution to the boson peak region by longitudinal acoustic mode modes that are characteristic of semicrystalline polymers and appear in the same low‐frequency region is discussed. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 2852–2859, 2001     

Isotactic poly(p-fluorostyrene): Conformation and molecular packing analysis

The chain conformation and molecular packing of isotactic poly(p-fluorostyrene) have been examined using calculations made with semiempirical potential energy functions. Isolated chain conformational energies indicate no difference in conformation for the fluoropolymer from the conformation for isotactic polystyrene. The energy for packing poly(p-fluorostyrene) chains into a crystalline array as 3₁ or 4₁ helices was also compared with the energies for packing polystyrene in both of these helical forms. While not being the lowest energy mode of packing for poly(p-fluorostyrene), the packing of 4₁-helices does yield a local energy minimum. Such packing of 4₁ helical polystrene chains is considerably less energetically feasible. The results indicate the causes for the experimentally observed difference in the crystalline conformations of the two isotactic polymers as being due to intermolecular influences.