重离子治癌装置研究

介绍了重离子治癌装置的最新发展状况 ,比较了两类典型的旋转机架的结构及光学特性 ,给出了离子光学的限制条件 .设计了一台桶形机架 ,为兰州重离子冷却储存环应用于医学治疗进行了预研. A simple plane rotating gantry is proposed at the Heavy Ion Research Facility in Lanzhou (HIRFL), where a new project named Cooling Storage Ring is under construction. The gantry is 18 metre long, 5 metre high from upper beam axes to rotation axes. It consists of eight quadruples, two 45° and one large aperture 90° dipole magnets. It is equipped with a two direction magnetic raster scanning system. A beam spot of radii between 2 to 5 mm can be achieved at∶...     

INVESTIGATION OF PHOTOREFRACTIVE TWO-WAVE COUPLING IN Cr-DOPED STRONTIUM BARIUM NIOBATE CRYSTAL

We present here the experimental results of photorefractive two-wave coupling in the congruent strontium barium niobate (SBN:61) crystal doped with 1000ppm Cr. Employing a He－Ne laser (632.8nm), we observed the coupling characteristics under different conditions. The crystal shows excellent photorefractive properties, with a high coupling coefficient nearly 6cm^-1 as the beam intensity ratio m is less than 100. The saturated coupling coefficient of SBN:61:Cr shows a maximum at a certain external beam crossing angle 2θ_peak, which varies with different m, showing a nearly linear dependence on m. The saturated coupling response time τ is measured to be less than 0.8 s. The response time decreased with increasing beam crossing angles no matter how large m is. We also observed the behaviour of the probe beam in reversed experimental procedures. We found that the probe beam shows a bistable state in both procedures.     

TRANSPORT PROPERTIES OF μc-Si:H FILMS PREPARED BY VERY HIGH HYDROGEN-DILUTED SILANE PLASMA

Highly hydrogen-diluted silane plasma is used to fabricate microcrystalline silicon films in a plasma-enhanced chemical vapour deposition system. X-ray diffraction and micro-Raman scattering spectroscopy are utilized to characterize their microstructure properties. Dark conductivity and drift mobility are measured by the travelling wave method. With the decreasing gas flow ratio of silane-to-hydrogen from 2% to 0.2%, the crystalline volume fraction and the drift mobility increase at room temperature. Meanwhile, the dark conductivity increases initially and then decreases. The relationship between the microstructures and transport properties is discussed.     

电极用纳米Ag2O的电化学性能研究Ⅲ.电极的循环伏安行为

研究了3种具有不同组成的氧化银（Ⅰ）电极在2种不同扫描条件下的循环伏安（CV）行为,发现在较慢扫速（0.5mV/s)条件下,不同组成电极的峰形相差较大。各电极的峰电流值都呈现出明显的差异,即具有合适配比的混配电极展示出良好的循环可逆性能,而纯纳米粒子组成的电极接受电荷的能力明显较强。对于各极峰位的偏移及峰电流的涨消做了对比解析,表明最佳混配电极中的电活性粒子具有合理的分布,电极极化小,活性物质利用率高,因而能够展示出良好的电化学性能。     

尖晶石LiMn_2O_4的表面改性研究

采用溶胶_凝胶法合成尖晶石LiMn2 O4 ,并以LiCoO2 对其进行包覆 ,用XRD、SEM、EPMA等方法对修饰的尖晶石结构和性能进行研究 .结果表明 ,经包覆的LiMn2 O4 在 70 0℃焙烧 10h所得的晶粒是表层富含Co的立方尖晶石 ,而且晶粒中Co3+的含量呈现出从表到里递减的梯度分布 .以该材料作锂离子电池正极 ,虽初始容量稍有降低 ,但能有效地降低Mn2 +在电解质中的溶解 ,而且对Jahn_Teller效应有一定的抑制作用 ,包覆的LiMn2 O4 尖晶石正极材料比未包覆的有更好的循环性能     

The Influence of Temperature on Ethene Diffusion in H[Al]ZSM-5 Studied by Molecular Dynamics

Molecular dynamics(MD) simulation of ethene diffusion in the lattice of H[Al]ZSM-5 was performed at the temperature ranging from 300 K to 700 K. The calculated diffusion coefficients increase with the temperature from 2.60×10-9 m2/s at 300 K to 12.78×10-9 m2/s at 700 K. The Arrhenius plot gives an activation energy of 6.31 kJ/mol. The anisotropy of the diffusion process was examined.     

苯并三氮唑对硫增感溴化银乳剂的过增感效应

采用在曝光前后用苯并三氮唑溶液对未增感的和硫增感的立方体溴化银乳剂涂层的处理方法,考察了苯并三氮唑在溴化银成像过程的两个阶段:曝光潜影的形成阶段和潜影中心得以放大的显影阶段的作用.有意义地发现苯并三氮唑对硫增感溴化银乳剂有明显的过增感效应.实验结果表明:1)对于未增感的立方体溴化银乳剂涂层,在曝光前吸附了苯并三氮唑后会抑制潜影的形成,但曝光后吸附了苯并三氮唑对显影有十分明显的促进作用;2)对于硫增感的立方体溴化银乳剂涂层,曝光前用苯并三氮唑溶液处理后,产生显著的过增感效应,相对感光度可提高4倍左右,在曝光后用苯并三氮唑溶液处理,随着苯并三氮唑浓度的增加对显影也有一定程度的促进作用;3)对于硫增感的溴化银涂层,先经过388 mV的氧化还原缓冲液处理,再经苯并三氮唑溶液处理过的样片的感光度都要较未经缓冲液处理的提高4倍左右,这说明苯并三氮唑对硫增感乳剂产生的过增感效应只与硫敏化中心内(Ag₂S)_n的存在有关,与(Ag)_m是否存在无关.     

薄层色谱法测定二磺化和三磺化 5H-苯基联苯膦氧化物的含量

采用薄层色谱法,对新型化合物5H-苯基联苯磷（PDBP）磺化产物的分离、二磺化和三磺化PDBP氧化物标准品的制备及其定量分析进行了研究。     

氯化聚乙烯的热可逆共价交联

采用新型热可逆共价交联剂 ,以溶液反应法使氯化聚乙烯 (CPE)交联制得了凝胶量在 80 %左右的共价交联CPE ,研究了不同牌号CPE、催化剂及其用量、反应温度、反应时间及交联剂用量对CPE交联程度的影响 ,并测定了共价交联CPE的热可逆转化特性     

Au/Pd(111)双金属表面催化噻吩加氢脱硫的反应机理

采用密度泛函理论（DFT）计算了Pd（111）表面含有N（N=1-4）个Au原子数目时的表面形成能,选取最优构型进一步研究了噻吩在Au/Pd（111）双金属表面的吸附模式及加氢脱硫反应过程. 结果表明：当Pd（111）表面含有1个Au原子时,其形成能最低. 在Au/Pd（111）双金属表面噻吩初始吸附于Pd-Hcp-30°位时,其构型最稳定. 在各加氢脱硫过程中,反应总体均放出热量. 对于直接脱硫机理,其所需活化能较低,但脱硫产物较难控制;对于间接脱硫机理,反应最有可能按照顺式加氢方式进行,C―S键断裂开环时所需活化能最高,是反应的限速步骤. 此外,与单一Au（111）面及Pd（111）面相比,Au/Pd（111）双金属表面限速步骤的反应能垒最低,表明AuPd双金属催化剂比Au、Pd单金属催化剂更有利于噻吩加氢脱硫反应的进行.