高功率氙灯脉冲放电过程中石英管壁热损伤机理

基于高功率激光装置对脉冲氙灯工程运行可靠性的要求,利用现有的能源模块开展了氙灯放电考核实验。实验结果表明：虽然氙灯运行在安全的能量负载水平,当能源模块单个放电回路的峰值功率超过300 MW时,氙灯石英玻璃管壁存在热损伤风险。肉眼观察到管壁损伤后在反射器对侧的灯管内壁出现乳白色沉积层。经扫描电镜和X射线光电子能谱测试分析,证实热损伤形成的乳白色沉积物为二氧化硅。为探究管壁热损伤机制,采用高速摄影观测了氙灯放电等离子体沟道发展过程。图像显示放大器内金属反射器的几何形状对放电沟道的分布产生了显著影响,尤其是在侧灯箱,灯内电弧沟道会靠近反射器一侧集中分布,因此,导致等离子体对灯管的偏烧。当放电峰值功率超过石英热负载极限时,管壁表面二氧化硅材料会被烧蚀至蒸发、气化,并随后沉积在灯管较冷部位。研究结果表明放电回路的放电峰值功率过高、放大器内金属反射器均会对氙灯造成热损伤。     

酸蚀与紫外激光预处理结合提高熔石英损伤阈值

采用HF酸刻蚀和紫外激光预处理相结合的方式提升熔石英元件的负载能力,用质量分数为1%的HF缓冲溶液对熔石英刻蚀1~100 min,综合透过率、粗糙度和损伤阈值测试结果,发现刻蚀时间为10 min的熔石英抗损伤能力最佳。采用355 nm紫外激光对HF酸刻蚀10 min的熔石英进行预处理,结果表明：紫外预处理能量密度在熔石英零损伤阈值的60%以下时,激光损伤阈值单调递增;能量到达80%时,阈值反而低于原始样片的损伤阈值。适当地控制酸蚀时间和紫外激光预处理参数能有效提高熔石英的抗损伤能力。     

Enhanced Photocatalytic Activity of Titanium Dioxide Supported on Hexagonal Mesoporous Silica at Lower Coverage

The photocatalytic activities of titanium dioxide (TiO₂) supported on hexagonal mesoporous silica (HMS), zeolite Y (NaY) were investigated by using the photodegradation of 2,4,6-trichlorophenol (TCP) as test reactions. It was found that the photocatalytic activity of TiO₂ on HMS was much higher than that of TiO₂ powders, and that of TiO₂ on NaY. It was also found that TiO₂/HMS had maximal photocatalytic activity at a lower Ti content. The larger the pore size of HMS used as the support of TiO₂, the better the photocatalytic activity of TiO₂ for degradating of organic pollutant. These observations suggested that the supported structure was a main factor responsible for enhancement of the photocatalytic activity of TiO₂. Characterization of the samples by TEM, XRD, BET, and UV-vis diffuse reflectance spectra indicated that the structures of HMS and TiO₂ were confirmed and TiO₂ did not enter into the HMS framework and was formed as nanoparticles on all supports.     

Chitosan‐Silica Sulfate Nano Hybrid as a Novel and Highly Proficient Heterogeneous Nano Catalyst for Regioselective Ring Opening of Epoxides via Carboxylic Acids

The synthesis and characterization of chitosan‐silica sulfate nano hybrid (CSSNH ) as a novel and efficient heterogeneous nano catalyst involving acid‐base bifunctional activity is described. The catalytic potency and activity of this eco‐friendly catalyst was investigated in regioselective ring opening of epoxides with carboxylic acids to access structurally diverse 1,2‐diol mono‐esters in good to excellent yields. CSSNH catalyst was characterized using different microscopic and spectroscopic techniques encompassing scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, N₂ adsorption isotherm, and Fourier transform infrared spectroscopy. The green nature, cheapness, efficiency, ease of preparation, handling and reusability of this new catalyst makes this catalyst to be useful for green industrial processes.     

Magneto-Optical Properties of Silica Gel Containing Magnetite Fine Particles

The magnetic composite materials that consist of transparent matrix and magnetic fine particles are expected to have large residual magnetization and coercive force because of their fine magnetic domain structure, and also to show magneto-optical effects. Silica gels containing magnetite (Fe₃O₄) fine particles were prepared by sol-gel method. The magnetic, optical and magneto-optical properties of the composites were investigated by measurements of magnetization curves, UV-visible spectra and Faraday rotation in visible range. The saturation magnetization of the composite was almost as same as that expected from the amount of magnetite fine particles in it. Although the composites had large and broad absorption at around 400 nm, they still maintained their transparency. The origins of decrement of transparency attributed to the optical absorption of magnetite and scattering due to magnetite fine particles. The whole composites showed positive Faraday rotation under external static magnetic field due to the large contribution of diamagnetic silica gel matrix. Magnetite contributed negative Faraday rotation with maximum at around 470–480 nm to the magneto-optical spectra of the composites.     

Freezing and Melting of Water Confined in Silica Nanopores

In nanosized pores, liquid water can be thermodynamically stable down to temperatures well below the limit of homogeneous nucleation of bulk water (～235 K). Studies of water in such pores therefore offer an opportunity to reveal the anomalous behavior of deeply supercooled water. Herein we focus on recent studies of the limits of freezing and melting of water in the cylindrical pores of ordered mesoporous silicas with pore diameters in the range of 2–10 nm, based on vapor sorption measurements, calorimetric studies, NMR spectroscopy and cryoporometry, and neutron diffraction studies.     

Preparation and adsorption property of novel inverse-opal hierarchical porous N-doped carbon microspheres

The design of pore structure is the key factor for the performance of porous carbon spheres.In this wo rk,novel micron-sized colloidal crystal microspheres consisting of fibrous silica(F-SiO_2) nanoparticles are firstly prepared by water-evapo ration-induced self-assembly of F-SiO_2 nanoparticles in the droplets of an inverse emulsion system to be used as sacrificial templates.Acrylonitrile(AN) was infiltrated in the voids of the F-SiO_2 colloidal crystal microspheres,and in-situ induced by ~(60)Co y-ray to polymerize into polyacrylonitrile(PAN).After the PAN-infiltrated F-SiO_2 colloidal crystal microspheres were carbonized and etched with HF solution,novel micron-sized inverse-opal N-doped carbon(IO-NC) microspheres consisting of hollow carbon nanoparticles with a hierarchical macro/meso-porous inner surface were obtained.The IO-NC microspheres have a specific surface area as high as 266.4 m~2/g and a molar ratio of C/N of 5.They have a good dispersibility in water,and show a high adsorption capacity towards rhodamine B(RhB) up to 137.28 mg/(g microsphe re).This work offers a way to obtain novel micron-sized hierarchical macro/meso-porous N-doped carbon microspheres,which opens a new idea to prepare high-performance hierarchical porous carbon materials.     

担载型铱催化剂上CO吸附量热和红外光谱研究

分别对Al2O3和SiO2担载的不同含量铱(Ir)催化剂进行了H2程序升温还原、CO微量吸附量热和红外研究.结果表明,还原后,Ir/Al2O3上存在金属态Ir0和氧化态Irδ 两种物种,CO在催化剂表面主要以线式和孪生吸附态存在,测量的CO吸附热为两种吸附形式的平均吸附热.提高还原温度和Ir担载量,Ir/Al2O3表面CO线式吸附物种的比例增加,从而导致CO吸附热值的升高.而在Ir/SiO2上Ir物种主要为金属态Ir0,CO吸附都以线式吸附为主,在所考察的条件下CO吸附热随Ir担载量和还原温度的变化不明显。     

水玻璃旧砂中的Na_2O

水玻璃砂铸型因受不同温度的作用，其断面浇注后变成７种不同的颜色．通过对７种不同色层旧砂的再生处理、化学分析和电性能测试，揭示了水玻璃砂型中的Ｎａ２Ｏ经高温浇注后的行为、在旧砂中的分布及其对水玻璃砂再生和再生砂性能的影响     

在Triton X—100存在下,用2-(5-溴-2-吡啶偶氮)-5-二乙胺基苯酚(5-Br-PADAP)分光光度测定方钍石中的钍

方钍石是钍来源的重要含钍矿物。目前测定钍的含量的方法较多,虽有用5-Br-PADAP测定钍的方法的报导,但未见有在triton X-100存在下,用5-Br-PADAP直接测定方钍石中钍的含量的报导。Triton X-100的存在,使测定的酸度增加,从而增加干扰元素的干扰比;并且增加了络合物的稳定时间。本文采用5-Br-PADAP作显色剂,在氯乙酸-氯乙酸钠缓冲体系中用triton X-100表面活性剂胶束增溶分光光度测定方钍石(人工样品)中钍的含量,获得较满意的结果。在25毫升中,钍的比耳定律范围在0～20微克,摩尔吸光系数为5.2×10~4升·摩尔~(-1)·厘米~(-1),Sandell灵敏度为0.0045微克钍(IV)/厘米~2。我们对两种含量的方钍石人工样品进行了测试,结果良好,回收率在97.3～101.4％之间,此方法可靠,精密度较高,误差符合微量组分的测定要求,我们对样品测定结果表示满意。