波片相位延迟的精确测量及影响因素分析

提出一种精确测量波片相位延迟的方法。将待测波片置于起偏器和检偏器之间,转动待测波片和检偏器至不同的位置并探测输出的光强,得到波片的相位延迟。采用光源调制技术和解调技术,抑制了连续光所无法克服的背景光干扰和电子噪声的干扰;将光路分为测量光路和参考光路,采用软件除法技术,消除了光源波动的影响,从而实现波片相位延迟的精确测量。详细分析了影响测量精度的误差因素,主要有光源波长变化、温度变化、入射角倾斜、转台转角误差和光源波动,计算了1064 nm波长时厚度为0.52 mm的λ/4多级结晶石英波片产生的相位延迟误差

Surface relief resonant Brewster niters with multiple channels

In this paper, a new type of resonant Brewster filters (RBF) with surface relief structure for the multiple channels is first presented by using the rigorous coupled-wave analysis and the S-matrix method. By tuning the depth of homogeneous layer which is under the surface relief structure, the multiple channels phenomenon is obtained. Long range, extremely low sidebands and multiple channels are found when the RBF with surface relief structure is illuminated with Transverse Magnetic incident polarization light near the Brewster angle calculated with the effective media theory of sub wavelength grating. Moreover, the wavelengths of RBF with surface relief structure can be easily shifted by changing the depth of homogeneous layer while its optical properties such as low sideband reflection and narrow band are not spoiled when the depth is changed. Furthermore, the variation of the grating thickness does not effectively change the resonant wavelength of RBF, but have a remarkable effect on its line width, which is very useful for designing such filters with different line widths at desired wavelength.

Structural and optical characterization of InAs nanostructures grown on high-index InP substrates

The structural and optical properties of InAs layers grown on high-index InP surfaces by molecular beam epitaxy are investigated in order to understand the self-organization of quantum dots and quantum wires on novel index surfaces. Four different InP substrate orientations have been examined, namely, (1 1 1)B, (3 1 1)A, and (3 1 1)B and (1 0 0). A rich variety of InAs nanostructures is formed on the surfaces. Quantum wire-like morphology is observed on the (1 0 0) surface, and evident island formation is found on (1 1 1)A and (3 1 1)B by atomic force microscopy. The photoluminescence spectra of InP (1 1 1)A and (3 1 1)B samples show typical QD features with PL peaks in the wavelength range 1.3-1.55 mu m with comparable efficiency. These results suggest that the high-index substrates are promising candidates for production of high-quality self-organized QD materials for device applications. (C) 1999 Elsevier Science B.V. All rights reserved.

混凝土薄壳球形水窖结构的优化设计

分析球形水窖空间结构的应力分布情况并进行几何尺寸优化,避免建设者根据经验来确定球形水窖的厚度、构造及混凝土标号,以节省建窖材料,同时防止应力不足而发生破坏。【方法】利用基于ANSYS平台新开发的窖体有限元分析软件,对实际中窖壁厚度为4和11 cm的混凝土薄壳球形水窖进行空间结构应力分析,同时以水窖耗材量最小为目标函数,以许用应力和变形量为约束条件,对其进行几何尺寸优化。【结果】计算得出窖壁厚度为4和11 cm的水窖最大拉应力分别为1 380.00和447.31 kPa,最大压应力分别为5 153.20和1 896.70 kPa;优化出空窖不利工况下容积为20,30和40 m3的球形水窖窖壁最佳厚度,即栗钙土地区分别为0.051,0.061和0.065m,黄土地区分别为0.050,0.059和0.062 m。【结论】经软件优化计算后的球形水窖结构,既能满足强度和刚度的要求,同时也最大限度地节约了材料用量;利用新开发的窖体结构优化分析软件,能够对球形水窖进行空间应力分析与结构优化,可以作为球形水窖设计软件。

STUDIES ON ORGANOLANTHANIDE COMPLEXES .40. SYNTHESIS AND X-RAY STRUCTURE OF BIS (2-METHOXYETHYLCYCLOPENTADIENYL) YTTRIUM AND YTTERBIUM TETRAHYDROBORATES

New bis (2-methoxyethylcyclopentadienyl) yttrium and ytterbium tetrahydroborates (Ln = Y, 1; Yb, 2) have been synthesized in good yield by the reaction of bis (2-methoxyethylcyclopentadienyl) lanthanide chlorides (Ln = Y, Yb) with sodium borohydride in THF at room temperature. The title complexes were characterized by elemental analyses, MS, H-1 NMR and IR spectra. The crystal structures of 1 and 2 have been determined by X-ray diffraction. 1 crystallizes from THF-n-Hexane in space group Pna2(1) with unit cell parametert: a = 1.2390(3), b = 1.1339(2), c = 1.1919 (2) nm and V = 1.6745(6) nm3 with z = 4 for D(c) = 1.39 g.cm-3.The structure was solved by direct method and refined to final R = 0.061 (for 1730 observed reflections). The Space group of 2 is Pna2(1) with unit cell parameters: a = 1.2399(6), b = 1.1371(5), c = 1.1897(2) nm and V = 1.6773(1) nm3 with z = 4 for D(c) = 1.72 g.cm-3, R = 0.038 (for 2157 observed reflections). The X ray structures and IR reveal the bidentate yttrium and ytterbium tetrahydroborate complexes with the intramolecular coordination bonds between lanthanide metal and ligand oxygen atoms.

镧系金属有机配合物的研究 XL.双(2-甲氧乙基环戊二烯基)钇和镱的硼氢配合物的合成及晶体结构

双(2-甲氧乙基环戊二烯基>氯化钇和镱,在THF中,室温与硼氢化钠发生置换反应,生成双(2-甲氧乙基环戊二烯基)硼氢化钇(1)和镱(2),产率分别为70和59%.它们都经红外光谱,质谱,~1HNMR和元素分析鉴定.将l和2在THF-已烷中重结晶,得到适用于X射线衍射分析的单晶.1的空间群为Pna2_1,晶胞参数:a=1.2390(3),b=1.1339(2),c=1.1919(2)nm,晶胞体积,1.6745(6)nm~3.D_o=1.39g·om~3,z=4,R=0.061;2的空间群为Pna2_1,晶胞参数:a=1.2399(6),b=1.1371(5),c=1.1897(2)nm,晶胞体积,1.6773(1)nm~3,D_c=1.72g·cm~(-3),z=4,R=0.038,1与2都是含有两个内配位键(Ln—O)的双齿型的单体结构.

SYNTHESIS AND CRYSTAL-STRUCTURE OF K4H2[PMO9V3O40].10H2O

The crystal structure of the title compound was determined from single crystal X-ray diffraction at -90-degrees-C. The complex crystallizes in the tetragonal P4/mnc, Z = 2, a = 12.515(3), c = 17.636(7) angstrom. The structure was solved by Patterson and Fourier techniques and refined by least-squares to R = 0.061 for 788 reflections. The central PO4 is disordered, P-O = 1.54 angstrom, M(M = Mo or V) is 6-coordinate, M-O = 1.62-2.48 angstrom, K is 7-coordinate, K-O = 2.84-3.10 angstrom.

K_4H_2[PMo_9V_3O_(40)]·10H_2O的合成及其晶体结构

采用低温技术,用 X 射线单晶衍射法测定了标题化合物的结构.晶体属 P4/mnc 空间群,a=12.515(3),c=17.636(7),Z=2.用788个独立可观测反射精修所有结构参数得 R=0.061.钼钒磷杂多酸阴离子中,PO_4四面体是无序的,P—O 键长1.54.M(Mo,V)是6配位,M—O 键长1.62—2.48.K 是7配位,K—O 键长2.84—3.10.

HPLC测定刺芒龙胆不同部位中3种有效成分的含量

目的：建立反相高效液相色谱法同时测定刺芒龙胆植物不同部位落干酸、獐牙菜苦苷、龙胆苦苷的含量。方法：采用ZORBAX SB-C18（250mm×4．6mm，5μm）色谱柱，流动相为甲醇-水（含0．04％磷酸）的比例25：75，流速1mL·min^-1，检测波长238nm，柱温30℃。结果：3种成分均达到基线分离，落干酸、獐牙莱苦苷、龙胆苦苷的线性范围分别为0．039～1．56μg（r=0．9998），0．0725～1．45μg（r=0．9999），0．061～1．225μg（r=0．9997）；回收率为101．3％（RSD=2．6％），98．7％（RSD=3．1％，99．6％（RSD=1．2％）。结论：测定方法快速，结果准确、可靠。