快速气相色谱控制系统的设计与应用

设计了一种用于快速气相色谱(Fast gas chromatography,FGC)的新型控制系统。该控制器主要由色谱柱温度控制系统、自动进样及气路压力控制系统组成。其温度控制范围为30~160℃,升温速度约为3℃/s,温度控制精度为±0.5℃,载气压力控制范围为0~0.5 MPa。将本控制器应用于自制快速色谱,并用色谱对由直链正构烷烃(C1~C8)以及甲苯9种物质组成的标准样品进行测试。结果显示,色谱能在100 s内将此9种物质完全分开。     

Suppression of Photoinduced BBO Defects Generation on TIO2（110） by Water

We have investigated creation of variable concentrations of defects on TIO2（110）-（1×1） surface by 266 nm laser using temperature programmed desorption technique. Oxygen-vacancy defects can be easily induced by ultraviolet light, the defects concentration has a linear dependence on power density higher than 50 mW/cm2 for 90 s irradiation. No observation of O2 molecule and Ti atom desorption suggests that UV induced defects creation on TiO2（110）-（1×1） is an effective and gentle method. With pre-dosage of thin films of water, the rate of defects creation on TiO2（110）-（1×1） is slower at least by two orders of magnitude than bare TiO2（110）-（1×1） surface. Further investigations show that water can be more easily desorbed by UV light, and thus desorption of bridging oxygen is depressed.     

Ni-Ti-O混合氧化物的制备、表征及其富氧选择性催化还原NO

采用均匀共沉淀法制备了不同Ni/Ti摩尔比的Ni-Ti-O混合氧化物,考察了它们在富氧条件下丙烯选择性催化还原NO反应中的催化性能,并运用X射线衍射,N₂吸附-脱附、吡啶吸附、程序升温脱附和原位红外光谱对催化剂进行了表征.结果表明,Ni/Ti摩尔比为1的催化剂表现出最佳催化活性,430℃时NO_x转化率达68%.该催化剂具有锐钛矿结构,比表面积较高(149m²/g),有利于提高催化活性;其表面Lewis酸性位有利于硝酸盐物种的吸附,而硝酸盐物种是该反应的重要中间体.     

“聚龙一号”装置上磁驱动铝飞片实验的数值模拟

采用二维磁驱动数值模拟程序MDSC2,对大电流脉冲装置"聚龙一号"上的151发次磁驱动370μm厚铝飞片实验、164发次磁驱动330μm厚铝飞片实验进行了数值模拟和分析。数值模拟表明:370μm厚铝飞片和330μm厚铝飞片的磁驱动过程中,VISAR测量的速度不是飞片自由面的速度,而是飞片中邻近自由面最近的固体反射面的速度。这是由于磁驱动飞片发射过程中,飞片自由面部分被烧蚀,密度低于固体密度状态,而飞片自由面和加载面中间的飞片还保持固体密度状态。VISAR测量的激光将穿过自由面的低于固体密度状态的飞片部分,到达飞片自由面最近的固体密度位置再反射回去,获得这一位置的飞片速度。数值模拟的飞片固体反射面速度历史和VISAR测量的速度历史相吻合。     

激光固体靶相互作用产生正电子的模拟研究

采用Monte Carlo程序Geant4对激光固体靶相互作用正电子产生进行了研究。研究了超热电子能量分布函数对正电子产生的影响,结果表明采用不同的分布函数,最多可致正电子产额约3倍的差异,分布函数的最大截止能量在30 MeV以上时正电子产额趋于饱和。研究了正电子产生与超热电子发散角的关联,结果表明发散角模型对正电子产额影响不大,而正电子角分布对超热电子发散角较为敏感,且靶背鞘场对正电子发散角的减小贡献巨大。模拟结果显示靶厚度的增加可导致正电子发散角的增大,而当靶厚度超过2mm时,发散角基本保持不变。此外,模拟了超热电子发散角、靶厚度及靶背鞘场对正电子电子份额比及正电子γ份额比角分布的影响。     

第二届东方胶化杯全国胶体与界面化学优秀青年学者奖评选通知

<正>宗旨为促进我国胶体与界面化学的发展,鼓励这一领域青年学者的创新进取,经研究决定自2013年起设立全国胶体与界面化学优秀青年学者奖,以表彰胶体与界面化学领域的青年优秀人才。申请资格与范围全国范围内各大学、科研机构内具有中国国籍的胶体与界面化学研究人员(不含博士后)均有资格申     

Ceric ammonium nitrate supported HY-zeolite：An efficient catalyst for the synthesis of 1, 8-dioxo-octahydroxanthenes

Ceric ammonium nitrate （CAN） supported HY-zeolite has been used as an efficient catalyst for the one- pot synthesis of 1,8-dioxo-octahydroxanthenes from the readily available 1,3-diketone and aromatic aldehydes under solvent-free conditions. The present methodology is cost-effective in addition to other advantages like high yields of products in shorter reaction time and simple workup procedure without the use of any injurious solvents.     

Coking-resistant Ni-ZrO2/A1203 catalyst for CO methanation

Highly coke-resisting ZrO2-decorated Ni/A1203 catalysts for CO methanation were prepared by a two-step process. The support was first loaded with NiO by impregnating method and then modified with ZrO2 by deposition-precipitation method （IM-DP）. Nitrogen adsorption- desorption, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, thermogravimetdc analysis, H2 temperature- programmed reduction and desorption, NH3 temperature-programmed desorption, and zeta potential analysis were employed to characterize the samples. The results revealed that, compared with the catalysts with the same composition prepared by co-impregnation （CI） and sequential impregnation （SI） methods, the Ni/A1203 catalyst prepared by IM-DP showed much enhanced catalytic performance for syngas methanation under the condition of atmospheric pressure and a high weight hourly space velocity of 120000 mL.g-1 .h-1. In a 80 h life time test under the condition of 300-600 ~C and 3.0 MPa, this catalyst showed high stability and resistance to coking, and the amount of deposited carbon was only 0.4 wt%. On the contrary, the deposited carbon over the catalyst without ZrO2 reached 1.5 wt% after a 60 h life time test. The improved catalytic performance was attributed to the selective deposition of ZrO2 nanoparticles on the surface of NiO rather than A1203, which could he well controlled via changing the electrostatic interaction in the DP procedure. This unique structure could enhance the dissociation of CO2 and generate surface oxygen intermediates, thus preventing carbon deposition on the Ni particles in syngas methanation.     

纳米复合材料CdS/TiO2制备与不同模式光催化降解多种染料

采用化学水浴沉淀法再结合溶胶-凝胶和程序升温溶剂热两步法制备了一系列不同比例的CdS/TiO2。通过XRD、XPS、SEM、UV-Vis/DRS等手段对所合成纳米复合材料的组成、结构和形貌等进行了表征。结果表明,该系列CdS/TiO2为锐钛矿TiO2和六方相CdS的混合晶相,其在可见光有较强吸收,并且随着复合材料中TiO2比例的增加,BET值明显增大。另外,所合成CdS/TiO2呈圆球形,颗粒比较均匀。紫外光催化降解甲基橙的实验结果表明,摩尔比为1:4的CdS/TiO2的活性明显高于CdS、P25以及其它不     

制备方法对Ni2P/SiO2催化剂结构及萘加氢性能的影响

采用程序升温还原法和次磷酸盐歧化法制备了Ni_2P/SiO_2催化剂,结合现代仪器分析表征技术,研究了制备方法对Ni_2P/SiO_2催化剂结构和萘加氢性能的影响。结果表明,两种方法均可制备出仅含Ni_2P活性相的Ni_2P/SiO_2催化剂,在反应温度340℃、氢气压力4 MPa、空速为20.8 h~(-1)下,程序升温还原法制备的Ni_2P/SiO_2催化剂表现出更高的萘加氢活性,这主要是因为程序还原法制备的Ni_2P/SiO_2催化剂中有更多Ni_2P物种生成,提供了较多的活性位点(CO吸附量21.6μmol/g);且催化剂表面弱酸位点多,有利于芳烃吸附。当选用程序升温还原法制备Ni_2P/SiO_2催化剂时,在保证生成纯相Ni_2P的前提下,较低的Ni/P比更有利于合成高加氢活性的Ni_2P/SiO_2催化剂。