Flexible and accurate implementation of a binocular structured light system

This paper presents a practical implementation of a binocular system for three-dimensional (3D) surface measurement. Manufacturing procedures are easy to implement because this system does not require that the optical axes of two cameras’ lenses be coplanar and the structured light sheets be perpendicular to that plane. The method of structured light calibration is proposed to obtain the parameters of the structured light sheets. This calibration method can tolerate the surface condition of the calibration board. To eliminate the effect caused by the distortion of projector lens, each structured light sheet is fitted to a conicoid. Meanwhile, data acquired from two cameras are transformed into a unique coordinate system to avoid 3D data matching. Experiments are conducted to validate the flexibility, accuracy, and desirability of our system.     

芳基芳酰基偶氮化合物的合成及其结构表征

以自制的芳基芳酰肼类化合物为原料,以NaBrO3/H2SO4为氧化体系,在室温下,将芳基芳酰肼类化合物氧化脱氢为芳基芳酰基偶氮化合物.产品的结构经元素分析、IR、1HNMR确证,收率为85%-93%.     

Surface chemistry and catalytic activity of Ni/Al2O3 irradiated with high-energy electron beam

The radiation effects induced effects by electron beam (EB) treatment on the catalytic activity of Ni/γ-Al₂O₃ were studied for the carbon dioxide reforming of methane with different EB energy and absorbed radiation dose. Transmission electron microscope (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) were used to determine the change in structure and surface states of Ni/γ-Al₂O₃ catalyst before and after the EB treatment. Higher energy EB treatment is useful for increasing the proportion of the active sites (such as Ni⁰ and NiAl₂O₄-phase) on the surface. The increase of Ni/Al-ratio indicates that the Ni dispersion on the surface increased with the EB-treatment, resulting in an increase of the active sites, which leads to improving the catalytic activity. XPS measurement also showed a decrease of the surface carbon with EB dose. The maximum 20% increase in the conversion of CO₂/CH₄-mixture into CO/H₂ gas was observed for the catalyst treated with 2 MeV energy and 600 kGy dose of EB relative to untreated.     

Photodegradation of CH3I on mesoporous TiO2-B nanofibers with Au nanoparticles

Au nanoparticles deposited on mesoporous TiO₂-B nanofibers have been prepared, characterized, and used to catalyze photoreactions of iodomethane. High-density gold-particle deposition on TiO₂-B is obtained by electrostatic and/or chemical force between the particles of TiO₂-B and Au capped with -SC(H)(CO₂H)(CH₂CO₂H) through pH control. The capping groups on the gold particles can be removed after 400 °C calcination. It is found that the nature of the inorganic acids used for pH adjustment has effects on particle morphology and deposition. Two other methods, i.e., preparation of TiO₂-B nanofibers in the presence of gold particles and preparation of gold nanoparticles in the presence of TiO₂-B particles (deposition-precipitation method), are also investigated. However, the former method produces a low-density deposition and the latter one induces a morphology change of the TiO₂-B and an increase of the Au in size. Fourier transform infrared spectroscopy has been employed to study and to compare the photoreactions of CH₃I on TiO₂-B and Au/TiO₂-B and the effect of O₂. The presence of gold particles on TiO₂-B increases the efficiency of CH₃I photodegradation, forming adsorbed methoxy and formate. The role of gold is also discussed.     

Reasons for the deactivation of Pt/TiO2 photocatalyst treated by inert gas N2

The effect of N₂ treatment on the photocatalytic activity of Pt⁰/TiO₂ was investigated. The results showed that after treatment at 500 °C in N₂, 70% of the photocatalytic activity of 1.0 wt.% Pt⁰/TiO₂ was lost by the evaluation of photocatalytic oxidation reaction of C₃H₆. Transmission electron microscopy (TEM) and Ar⁺ ion sputtering tests revealed that in the course of high-temperature N₂ treatment, the size of Pt⁰ particles on TiO₂ increases and a strong interaction between metal and support, i.e. Pt⁰ particles encapsulated by Ti_xO_y, happens, which are the reasons for the deactivation of Pt⁰/TiO₂ photocatalyst treated by high-temperature N₂.     

温度和振动对光纤马赫-曾德干涉仪的影响与动态补偿研究

环境温度变化和振动会引起光纤马赫-曾德干涉仪两臂相差随机性变化,致使干涉仪输出不稳定.本文研究了自然条件下外界温度和振动对基于3×3耦合器干涉仪的影响,分析结果表明,温度和振动所引起的干扰主要集中于100Hz以下的低频成分中.为了消除这些干扰,设计了单臂补偿的反馈回路以稳定输出信号,并提出了一种利用象限判决方法来区分反馈正负性的动态补偿方法.实验中利用3×3耦合器3个输出端中其中2个进行光电变换、差分放大等反馈电路后驱动管状压电陶瓷,使缠绕在其上的光纤伸缩,动态补偿干涉仪相差的漂移,稳定干涉仪输出即3×3耦合器第三输出端口的信号.针对自然环境下温度和振动引起的干扰,本文研制了一种稳定的动态补偿装置,能有效抑制160Hz以下的低频干扰,实时补偿干涉仪两臂的相差漂移,干涉仪输出稳定的干涉信号,波动幅度小于5.64%.     

Synthesis, structural and magnetic properties of the nanocomposite Fe63B23Nd7Y3Nb3Cr1 magnets

The Fe₆₃B₂₃Nd₇Y₃Nb₃Cr₁ nanocomposite magnets in the form of sheets have been prepared by copper mold casting technique. The phase evolution, crystal structure, microstructural and magnetic properties have been investigated in the as-cast and annealed states. The as-cast sheets show magnetically soft behaviors which become magnetically hard by thermal annealing. The optimal annealed microstructure was composed of nanosize soft magnetic α-Fe (19-29 nm) and hard magnetic Nd₂Fe₁₄B (45-55 nm) grains. The best hard magnetic properties such as intrinsic coercivity, _jH_c of 1119 kA/m, remanence, B_r of 0.44 T, magnetic induction to saturation magnetization ratio, M_r/M_s=0.61 and maximum energy product, (BH)_max of 55 kJ/m³ was obtained after annealing at 680 °C for 15 min. The annealing treatment above 680 °C results in non-ideal phase grains growth, which degrade the magnetic properties.     

Energy transfer between activators at different crystallographic sites in Sr3SiO5:Eu

A yellow phosphor, Sr₃SiO₅:Eu²⁺, was synthesized by a high temperature solid-state method. Sr₃SiO₅:Eu²⁺ exhibits a single yellow emission under the blue radiation excitation. However, Sr₃SiO₅:Eu²⁺ shows a two-peak emission under the ultraviolet radiation excitation when Eu²⁺ doping content is less than 0.01 mol. Moreover, the blue emission disappears and the yellow emission reaches the peak value when Eu²⁺ doping content is 0.01 mol. Namely, the energy transfer takes place between the Eu²⁺ activators, which is located at two different crystallographic sites in the Sr₃SiO₅. And the energy transfer mechanism is the dipole-dipole interaction.     

Near-infrared luminescence of OH and Cl doped Bi4Ge3O12 crystals

OH⁻ and Cl⁻ doped Bi₄Ge₃O₁₂ (BGO) single crystals had been grown by Vertical Bridgman (VB) method. The structure of these crystals was determined by XRD, the transmittance and emission spectra in near infrared region (NIR) were measured at room temperature. 5% OH⁻ doped BGO shows a significant emission band peaking around 1181 nm under 808 nm laser diodes (LDs) excitation, and the 5% Cl⁻ doped BGO exhibits a relatively weak emission band as well. 100% and 5% OH⁻ doped BGO show noticeable emission band centered at about 1346 nm under 980 nm LDs excitation.     

(S)-1-苄基-3-羟基吡咯烷的合成及红外光谱研究

从L-苹果酸出发,经过与苄胺缩合反应得到(S)-1-苄基-3-羟基吡咯烷-2,5-二酮,再通过硼氢化钠-碘体系还原制得重要的医药中间体(S)-1-苄基-3-羟基吡咯烷。采用红外光谱法对原料、中间体及产物进行了测试并对硼氢化钠-碘体系还原酰亚胺的机理进行了研究。通过比较原料、中间体及产物相应特征吸收峰的消失或是出现,可知所得的产物为(S)-1-苄基-3-羟基吡咯烷;还原机理研究表明,硼氢化钠在碘催化下生成的硼烷与酰亚胺中的羰基形成四元环状过渡态,同时另外一分子硼烷与酰亚胺中的氮原子形成N-BH3复合物,然后羰基还原完全,得到(S)-1-苄基-3-羟基吡咯烷-硼烷复合物,最后在甲醇作用下脱去硼烷得到最终产物。