TiO2柱撑蒙脱土的制备及其对品红降解的催化反应

基于TiO2光催化剂的优良光催化活性,采用酸性溶胶法合成了TiO2柱撑蒙脱土复合光催化剂,利用IR,UV-Vis,TG/DTA,XRD及SEM等手段对复合催化剂进行了表征,通过太阳光对酸性品红光催化降解实验,考察了催化剂的光催化活性。该催化剂比纳米TiO2对酸性品红的光催化降解反应表现出更高的催化活性,而且更易于沉降、回收。当TiO2柱撑蒙脱土光催化剂的用量为0.2 g.(100 mL)-1,酸性品红溶液的pH值为3时,在太阳光下40 min内酸性品红基本降解完全,而且该降解过程符合Langmuir-Hin-shelwood方程。X射线衍射(XRD)分析表明钛柱撑蒙脱土的层间距较钠基蒙脱土有明显的增大,紫外-可见吸收光谱表明TiO2柱撑蒙脱土比纳米TiO2具有更高的光吸收效率。     

Pr掺杂TiO2光催化剂的制备及其对酸性品红降解反应的催化性能

以钛酸四丁酯为前躯物,采用溶胶-凝胶法制备了掺杂不同含量Pr的TiO2光催化剂,利用XRD,TG-DTA,AFM,UV-Vis,FTIR等手段对催化剂进行了表征。并通过酸性品红光催化降解实验对其光催化性能进行了评价,考查了实验条件,如催化剂用量,烧结温度,掺杂量等对催化剂催化活性的影响。Pr2O3的掺杂阻碍了TiO2晶相由锐钛矿型向金红石型的转变,使TiO2的粒径减小,比表面积增大,催化活性增强。当Pr掺杂量为0.8%,催化剂用量为0.03g,烧结温度为500℃时,酸性品红的降解率达到97%以上,酸性品红的降解反应为准一级反应。     

不锈钢材料及TiN镀膜处理后PSD测试实验研究

PSD性能是评价电子储存环真空室材料及材料表面处理优劣的一个重要指标. 对一约1.5m长不锈钢管道真空室进行了镀TiN薄膜处理, 并在合肥光源机器研究用光束线(MSB)的PSD实验站上对该真空室在镀TiN薄膜处理前后分别进行了PSD性能测试实验研究. 测试研究结果表明, 镀TiN薄膜处理对于减小不锈钢材料PSD有非常明显的作用.     

溶胶-凝胶SiO2酸性膜与碱性膜的激光损伤行为

 采用溶胶-凝胶技术分别在K9基片上镀制了光学厚度相近的单层SiO₂酸性膜和碱性膜。测试了两类薄膜的激光损伤阈值;分别采用透射式光热透镜技术、椭偏仪、原子力显微镜、扫描电镜和光学显微镜研究了两类薄膜的热吸收、孔隙率、微观表面形貌、激光辐照前薄膜的杂质和缺陷状况以及激光辐照后薄膜的损伤形貌。实验结果表明：相对于碱性膜,酸性膜有更大的热吸收和更小的孔隙率,因此其激光损伤阈值较小;两类薄膜不同的损伤形貌与薄膜的热吸收系数与微观结构有关。     

光学薄膜膜厚自动控制系统的研究

介绍了一种利用光电极值法同时控制规整膜系和非规整膜系的方法,利用VC++编写程序实现对光学监控信号的采集、处理及停镀点的自动判断,实现了规整膜系和非规整膜系膜层厚度的自动控制.并利用该膜厚自动控制系统实验制备了规整膜系和非规整膜系多层膜,实验结果表明：利用该系统镀制的薄膜重复性良好,且光谱曲线和理论光谱曲线吻合较好.该系统解决了非规整膜系的监控问题,由计算机控制膜层的停镀点,排除了人的主观因素对薄膜的性能及其制备的重复性产生的影响,提高了薄膜镀制的重复性和成品率.     

不锈钢材料及TiN镀膜处理后PSD测试实验研究

PSD性能是评价电子储存环真空室材料及材料表面处理优劣的一个重要指标.对一约1.5m长不锈钢管道真空室进行了镀TiN薄膜处理,并在合肥光源机器研究用光束线(MSB)的PSD实验站上对该真空室在镀TiN薄膜处理前后分别进行了PSD性能测试实验研究.测试研究结果表明,TiN薄膜处理对于减小不锈钢材料PSD有非常明显的作用.     

纳米结构锌及锌氧化物薄膜对甲基橙的降解作用研

采用磁控溅射方法制备了纳米金属锌薄膜,结合后续的空气退火处理制备了纳米锌氧化物薄膜. 金属锌薄膜对甲基橙的还原降解以及锌氧化物薄膜对甲基橙的光催化降解过程都可以用一级反应动力学方程来描述. 甲基橙溶液在金属锌膜的还原降解下具有最快的褪色速率,但矿化不完全：在紫外光波段出现的额外吸收峰表明生成了芳香族中间产物. 完全氧化的氧化锌薄膜对甲基橙的光催化降解速率仅为金属锌膜还原降解速率的1/4左右,没有出现芳香族中间产物. 另外实验发现部分氧化的锌氧化物薄膜对甲基橙的光催化降解速率明显高于完全氧化的氧化锌薄膜,光催化活性的提高可能由于部分氧化薄膜中同时存在的金属锌及氧化锌相之间的协同效应.     

LaCoO3光催化降解染料酸性红B的实验研究

采用硬脂酸溶胶凝胶法合成出钙钛矿型复合氧化物LaCoO3,并以其为催化剂对染料酸性红B进行降解实验.以高压汞灯为光源,研究了催化时间、催化剂用量、起始浓度以及溶液pH值对降解率的影响.在优化条件下,100mL、10mg/L酸性红B溶液用0.25g催化剂降解2h,降解率达到88.70%.     

Ta_2O_5薄膜的低能离子辅助蒸镀

用低能氧离子辅助蒸镀技术,制备了一系列Ta_2O_5薄膜.观测了薄膜的微结构,测量了薄膜的光吸收和光散射.实验指出,离子束轰击和基片加热同时进行,能够制得透明而匀均的Ta_2O_5薄膜.     

不锈钢管道低温溅射镀TiN薄膜技术

 设计了一套适用于加速器细长管道真空室的低温溅射镀TiN薄膜装置。利用该装置，对86 mm×2 000 mm的不锈钢管道真空室进行溅射镀TiN膜实验，并对镀膜实验结果进行分析，得到了适用于加速器管道真空室内壁溅射镀TiN膜的表面处理参数。样品测试结果表明：在压强为80～90 Pa、基体温度为160~180 ℃的镀膜参数下，不锈钢管道内壁获得的TiN薄膜最佳，薄膜沉积速率为0.145 nm/s。镀膜后真空室的二次电子产额明显降低。     

Size effect of gold nanoparticles on the electrocatalytic oxidation of carbon monoxide in alkaline solution

This paper describes preliminary findings of Au nanoparticle on glassy carbon (GC) electrodes for electro-oxidation of carbon monoxide in basic conditions. Electrochemical cyclic voltammetric results showed that CO oxidation simultaneously occurred in the anodic and cathodic sweeps during one cycle, and CO electro-oxidation activity was remarkably different in the anode for the different sized Au nanoparticles. The ultrafine catalyst metal particles (2 and 6 nm Au) were more active compared to the larger ones (12, 24 and 41 nm Au). The dependence of the activity on the particle size can be explained in terms of their effect on the number of active sites and the different surface gold oxide species.     

甘草多糖活性炭脱色工艺

研究了甘草多糖活性炭脱色的工艺.以脱色率为评价指标,在单因素筛选的基础上,采用正交试验法对脱色工艺进行优选.实验表明,脱色的最佳条件为温度40℃、时间40min、pH 5.0、活性炭添加量1.5％.该脱色工艺具有一定的推广价值.     

The research on the interfacial compatibility of polypropylene composite filled with surface treated carbon fiber

Dielectric barrier discharges (DBD) in ambient air are used on carbon fiber to improve the fiber surface activity. Carbon fibers with length of 75 μm are placed into the plasma configuration. The interaction between modified carbon fibers and polypropylene (PP) was studied by three-point bending (TPB) test. The chemical changes induced by the treatments on carbon fiber surface are examined using X-ray photoelectron spectroscopy (XPS). XPS results reveal that the carbon fiber modified with the DBD at atmospheric pressure show a significant increase in oxygen and nitrogen concentration. These results demonstrate that the surface of the carbon fiber is more active and hydrophilic after plasma treatments using a DBD operating in ambient air.     

介观尺度下活性炭微粒的光镊捕捉、点火和扩散燃烧特性研究

为探索介观尺度下固体燃料微粒的燃烧现象,本文提出采用光镊工具对活性炭微粒进行捕捉、悬浮、定位,再通过激光点燃,研究其着火及扩散燃烧特性.介观尺度燃烧室中,光镊捕捉7.0μm活性炭微粒的最低捕捉功率为3.2 mW,捕捉速率范围为103.7—70.0μm/s;活性炭微粒在静止气流中的最低点火功率为3.2 mW,颗粒的等效粒径、周长、面积和圆形度对最低点火功率影响甚微,点火延迟时间约48 ms,提高点火功率,点火延迟时间缩短,最小点火延迟时间小于6 ms;活性炭在着火后先发生无焰燃烧,紧接着发生有焰燃烧,无焰燃烧的扩散燃烧速率满足粒径平方直线规律,其燃烧速率范围为15.0—8.0μm/s;有焰燃烧的火焰面积和强度随燃烧时间发生闪烁,其闪烁频率约29.1 Hz.对于粒径为3.0μm的活性炭微粒,从加热到完全燃烧殆尽所需时间约0.648 s.结果表明:对于聚焦后的高能激光束点燃活性炭微粒的着火属于联合着火模式,在挥发份析出之前,活性炭非均相着火而发生无焰燃烧,挥发份析出后被点燃发生均相着火,火焰面始终保持圆形.     

Performance of C/C electric double layer capacitors with coal-based active carbon electrodes

Coal-based active carbon was prepared and used as electrodes of electric double-layer capacitors (EDLCs). The performance of EDLCs using active carbon electrodes with different pore structure was studied, including cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. With an increase of sodium hydrate/coal ratio, the pore structure of active carbon is greatly improved, resulting in larger double-layer capacitance. The capacitance of asymmetric EDLC is up to 65.98 F/g. Moreover, it is found that different pore structure of active carbon is necessary for positive and negative electrodes. Asymmetric EDLC not only exhibits high capacitance but also shows excellent charge-discharge performance, suggesting that it is very suitable and promising to design electrode materials for supercapacitors.     

Effect of oxygen surface groups on adsorption of benzene derivatives from aqueous solutions onto active carbon samples

The process of adsorption of selected benzene derivatives from aqueous solution is investigated on two carbonaceous materials of differentiated surface properties - quantity of oxygen functional groups. Carbon samples were prepared by removal of external layers from granules of unmodified and oxidized active carbon. The surface and structure characteristics of carbon samples were estimated by various methods. The experimental isotherms of organics adsorption from liquid phase were measured and interpreted in terms of the theory of adsorption on heterogeneous solid surfaces. The influence of differences in adsorbate and adsorbent properties on adsorption uptake was analyzed. The adsorption effectiveness was regarded as a result of the differences in adsorbate hydrophobicities and the effect of specific interactions of its functional groups with active sites on carbon surface.     

Photocatalytic activity and characterization of sol-gel-derived Cr(III)-doped TiO2-coated active carbon composites

Cr(III)-doped, TiO₂-coated active carbon (Cr–TiO₂/AC) were prepared by a sol–gel method. The effect of supports, including TiO₂ and active carbon (AC), on the molecular structure and photocatalytic activity of chromium oxide for complete decomposition of EDTA has been examined with respect to the content of Cr on the catalyst surface. The photocatalytic activity of the Cr–TiO₂/AC composites was evaluated in the decomposition of EDTA solution under UV irradiation. The results indicate that Cr–TiO₂/AC has a higher efficiency in decomposition of EDTA than TiO₂, TiO₂/AC or active carbon. This was attributed to the different functions of active carbon and chromate species. (1) Nanosize TiO₂ particles on composites were not reunited, possible because active carbon retards transformation of anatase into rutile and decreases the crystallite size. (2) Production of high concentrations of organic compound near Cr–TiO₂. (3) Carbon in active carbon causes some of the TiO₂ to reduce to Ti³⁺ ions, which prevents electron–hole pair recombination. (4) Formation of polychromate species, with a stronger redox capability, on the surface of TiO₂/AC. It was found that the addition of Cr to TiO₂ sol could suppress the grain growth of TiO₂ crystals and increase the hydroxyl content on the surface of TiO₂/AC. The photocatalytic efficiency and activity of the composites remained good, even after three cycles.     

碳纳米管拉曼光谱的温度效应

碳纳米管拉曼光谱的温度效应黄福敏１余国滔２谭平恒１张树霖１（北京大学物理系１和生命科学院２北京１００８７１）施祖进周锡煌顾镇南（北京大学化学与分子工程学院北京１００８７１）ＴｅｍｐｅｒａｔｕｒｅＥｆｆｅｃｔｏｆｔｈｅＲａｍａｎＳｐｅｃｔｒａｏｆＣａｒ...     

The influence of oxidation with nitric acid on the preparation and properties of active carbon enriched in nitrogen

The effect of oxidation by 20% nitric acid on the properties and performance of active carbons enriched with nitrogen by means of the reaction with urea in the presence of air has been studied. The study has been made on demineralised orthocoking coal and the carbonisates obtained from it at 600 or 700 °C, subjected to the processes of nitrogenation, oxidation and activation with KOH in different sequences. The amount of nitrogen introduced into the carbon with the aid of urea has been found to depend on the stage at which the process of nitrogenation was performed. The process of oxidation of the demineralised coal and the active carbon obtained from the former has been found to favour nitrogen introduction into the carbon structure. In the process of nitrogenation of the carbonisates the amount of nitrogen introduced has inversely depended on the temperature of carbonisation. The modifications of the processes permitted obtaining materials of different textural parameters, different acid-base character of the surface and different iodine sorption capacity.     

Green method for efficient PdNPs deposition on carbon carrier in the microreactor system

The synthesis of palladium nanoparticles and conditions of their deposition on active carbon fibers in the microreactor was described. All processes related with metal ion reduction, nucleation, and autocatalytic growth of particles as well as their deposition were carried out in the microreactor in only one cycle. Synthesis of palladium nanoparticles was carried out under different conditions, i.e., changing the initial concentration of metal ions and the reductant, at 40 °C. Depending on the conditions imposed, the nanoparticles of different size (hydrodynamic radius change from 12 to 37 nm) and shape (spherical, cube, pyramid) were obtained. It was also shown that flow conditions allow for much more efficient Pd deposition on active carbon fibers than the process carried out in the batch. It was observed that for concentrations of Pd(II) ions higher than 0.2 mM, the degree of fiber surface coverage increased significantly in comparison with the batch process.