基于红外连续变焦的坦克装甲车辆夜视系统设计

为了提高坦克装甲车的夜间作战能力,针对坦克装甲车辆作战范围,设计了一种红外连续变焦夜视系统,该系统可以进行昼夜连续完全被动的监控,能够在全黑夜晚和恶劣天气条件下使用,使车长在夜晚同样可以完成观察战场、搜索目标、指示目标和实施超越射击的任务.此红外连续变焦系统可实现焦距在50～200 mm范围内的变化调整,实现4倍光学连续变焦,且具有成像质量高、体积小等特点,不仅能够对特定的景物进行光学的放大缩小,并且在切换的过程中不会造成目标的丢失.     

气质联用法测定电视外壳中十种多溴二苯醚

建立了电视机外壳样品中10种多溴二苯醚的微波萃取-气质联用测定方法。10种多溴二苯醚的定量峰面积与其浓度在一定范围内成线性关系,检出限从0.08μg/m L到0.60μg/m L。采用索氏萃取法进行方法验证,测试结果的RSD≤2.83,两种方法经t检验无显著性差异。该方法具有简便、快速、试剂消耗量少的优点,可应用于电视机等国推污染控制认证产品塑料材料中多溴二苯醚测定。     

随机参差重频法抗雷达导引头距离波门前拖研究

文章分析了DRFM距离拖引干扰的工作原理,建立了干扰的信号模型。根据自动增益控制(AGC)变化对干扰进行了检测,在此基础上利用随机参差重频的方法对距离波门前拖进行抑制,在不同的干信比下分别进行了外场试验验证,通过对试验结果的分析表明了该方法能够有效的抑制干扰。     

Hydrothermal synthesis and structural characterization of a one-dimensional coordination polymer [Zn(Pydc)(Dppz)] n (H2Pydc = 2,6-pyridinedicarboxylic acid, Dppz = dipyrido[3,2-a:2′,3′-c]phenazine)

A new metal-organic coordination polymer [Zn(Pydc)(Dppz)] _n (I) (H₂Pydc = 2,6-pyridinedicarboxylic acid, Dppz = dipyrido[3,2-a:2′,3′-c]phenazine) was hydrothermally synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The X-ray diffraction analysis reveals that I crystallizes in the monoclinic system, space group P2₁/c. The Pydc^2? ligands adopt O,N,O′-tridentate chelating and monodentate bridging coordination mode to link two adjacent Zn2+ ions to form a one-dimensional (1D) zigzag chain. The adjacent chains are further linked through hydrogen bonds and π-π stacking interactions, forming a three-dimensional (3D) supramolecular framework. The unit cell parameters for I: a = 7.332(3) Å, b = 36.023(9) Å, c = 7.8838(13) Å, β = 105.65(3)^○, V = 2005.1(10) ų, Z = 4.     

Quick estimation of the Dpb for predicting the strength of chemical bond in situ

An approximate method has been established to calculate the depth of the potential acting on an electron in a molecule at the saddle point along a chemical bond, denoted by Dpb. It is a new indicator which can be used for predicting the strength of a chemical bond. In this work, as a practical application for demonstrating thismethod, we calculated the Dpb of deoxyribonucleosides and ribonucleosides along all C-H and N-H chemical bonds using the method. The results are in fair agreement with those results of previously reported experimental and theoretical observations.     

Alginate‐Based Microcapsules with a Molecule Recognition Linker and Photosensitizer for the Combined Cancer Treatment

A reactive template method was used to fabricate alginate‐based hydrogel microcapsules. The uniform and well‐dispersed hydrogel capsules have a high drug loading capacity. After they are coated by a folate‐linked lipid mixture on the surface, the capsules possess higher cell uptake efficiency by the molecule recognition between folate and the folate‐receptor overexpressed by the cancer cells. Moreover, in this bioconjugate, the lipid could remarkably reduce the release rate of hydrophilic doxorubicin from the hydrogel microcapsules and encapsulate the hydrophobic photosensitizer hypocrellin B. The biointerfaced capsules could be used as drug carriers for combined treatment against cancer cell proliferation in vitro; this was much more effective than chemotherapy or photodynamic therapy alone.     

Efficient One-Pot Synthesis of Benzimidazoles Under Solvent-Free Conditions

A green, efficient method for the synthesis of various 2-aryl-benzimidazoles in the presence of hypervalent iodine as the oxidant at room temperature under solvent-free conditions is reported. The salient features of this method include mild conditions, short reaction times (3–5 min), excellent yields, and simple procedure.     

Reductive Coupling of Aldehydes,Ketones and Aroyl Chlorides Induced by LVT Prepared from TiCl4/Al System

Aluminium powder has been used to reduce titanium tetrachloride to generate the low valent titanium (LVT)reagent which can induce the reductive coupling of aldehydes and ketones to form the corresponding pinacols or olefins. However, arylsulfonyl chlorides will give diaryldisulfides under the same condition.     

Diastereoselective Synthesis of γ-Butenolides Catalyzed by Potassium tert-Butoxide

Potassium tert-butoxide (0.1 mol%) catalyzed a vinylogous Mukaiyama aldol reaction between aromatic and aliphatic aldehydes with 2-(trimethylsilyloxy)furan. The corresponding γ-butenolides were obtained in good yields with good diastereoselectivities.     

Electrophoretic separation of gold nanoparticles according to bifunctional molecules‐induced charge and size

Gold nanospheres modified with bifunctional molecules have been separated and characterized by using agarose gel electrophoresis as well as optical spectroscopy and electron microscopy. The electrophoretic mobility of a gold nanosphere capped with 11‐mercaptoundecanoic acid (MUA) has been found to depend on the number of MUA molecules per gold nanosphere, indicating that it increases with the surface charge of the nanoparticle. The extinction spectrum of gold nanospheres capped with MUA at an MUA molecules per gold nanosphere value of 1000 and connected via 1,6‐hexanedithiol (HDT) decreases by 33% in magnitude and shifts to the red as largely as 22 nm with the increase of the molar ratio of HDT to MUA (R_HM). Gold nanospheres capped with MUA and connected via HDT have been separated successfully using gel electrophoresis and characterized by measuring reflectance spectra of discrete electrophoretic bands directly in the gel and by monitoring transmission electron microscope images of gold nanoparticles collected from the discrete bands. Electrophoretic mobility has been found to decrease substantially with the increment of HDT to MUA, indicating that the size of aggregated gold nanoparticles increases with the concentration of HDT.