电子光学中四极场分布的半解析法计算

 采用一种新的半解析法,对电子光学中3种不同形状电极产生的四极场进行分析计算。半解析法中极点的确定方法简单有效,可以结合电极的形状填充等效源,并且极点位置确定极为精确。在四极场的计算中,该方法具有表达式简单,求解变量少,而且计算精度和效率高的优点。对凸圆柱电极、内凹圆柱电极以及平板电极产生的四极场进行了求解,并将计算结果进行了比较,应用半解析法在计算凸圆柱电极产生的四极场具有更为明显的优势,精度可达0.001%。由于半解析法可得出标量电位函数的解析级数表达式,因此,场强的计算更加简便,同时也更容易保证场强的计算精度,这也有利于四极场的设计和优化。     

Synthesis and Properties of Axial Coordination Reaction of Unsymmetric Leucine Zinc(Ⅱ) Tetraphenylporphyrin with Pyrimidine

In recent years much work has been done on the syntheses and properties of axial coordination reaction of zinc tetraphenylporphyrins with nitrogenous donors in order to better understand the detailed molecuar mechanism of natural zincous enzymes. However,only a few studies have been reported in which the nitrogenous donors are bound to the amino acid metallotetraphenylporphyrins with unsymmetric structures. In this paper, a new unsymmetric leucine tetraphenylporphyrin, 5-(4-leucine butoxyphenyl)-10,15,20-triphenylporphyrin (H₂[Leu-TPP]) and its Zn(Ⅱ) complex (Zn[Leu-TPP]) are synthesized. Their structures are characterized by elemental analysis, UV, IR, fluorescense spectra. The changes of the electronic absorption spectra of axial coordination reaction of Zn[Leu-TPP] with pyrimidine in chloroform are investigated Coordination number (n) and equilibrium constant (β) of the reaction are measured by visible spectra techniques. The changes of standard molar enthalpy (Δ_rH_m^⊙) and molar entropy (Δ_rS_m^⊙) of the reaction are calculated. The obtained data are listed in table 1.     

Nonlinear Waves in Two-Dimensional （2D） Square Lattice Frenkel-Kontorova （FK） System

A 2D square lattice is studied. By using the continuum approximation, we set up the differential equations of motion for an arbitrary particle in the square lattice which subjects to an external periodic substrate potential. The exact solitary waves of the system are found for special cases. We conclude that the adhesive force f and the angle between propagation directions of upper and lower layers can affect these waves.     

超小孔径树枝状介孔二氧化硅纳米球的制备和表征

采用短碳链的表面活性剂溴代十二烷基三甲基溴化铵为模板剂,合成了具有较大粒径和超小孔径分布的单分散树枝状介孔二氧化硅纳米球(记为DMSNs-C12).通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线衍射能谱(XRD)、傅里叶变换红外光谱(FT-IR)、以及氮气吸附脱附曲线对制备的DMSNs-C12进行了形貌、晶体结构、化学组成、孔体积、比表面积等分析.结果表明:与传统的、以溴代十六烷基三甲基溴化铵为模板剂制备的单分散树枝状二氧化硅纳米球相比(DMSNs-C16),DMSNs-C12颗粒尺寸明显增大,褶皱结构消失,孔道尺寸急剧减小.原因是随着碳链减小,表面活性剂相互斥力减弱,影响微乳液形成,最终导致结构差异.     

CdWO4纳米晶形貌可控合成

分别以氯化镉、草酸镉、碳酸镉、柠檬酸镉和钨酸钠为原料,在没有采用模板和表面活性剂的条件下,采用水热法可控制备出了钨酸镉纳米颗粒、纳米棒、纳米束和纳米线.利用X射线衍射(XRD)、透射电镜(TEM)、高分辨透射电子显微镜(HRTEM)和选区电子衍射(SAED)对样品进行了表征.结果表明:[WO42-]/[Cd2+]摩尔比、反应时间及先驱体的类型对产物的形貌和尺寸有着重要的影响.     

胆甾相液晶的相诱导双轴性

采用胆甾相液晶的格胞理论,运用一定的统计方法,导出分布函数,定义序参数张量,由此推导出自由能表达式．在定域坐标系中,对胆甾相的长程取向序参数Ｓ和相诱导双轴序参数Δ进行了数值计算．所得的结果较前人有了不同程度的改善,和实验接近 关键词：     

氧等离子体对以石墨为碳源合成的CVD金刚石颗粒的影响

采用一种新型的金刚石颗粒制备方法,利用微波辅助化学气相沉积技术,向反应室内通入氢气,以固态石墨片同时作为碳源和衬底沉积金刚石颗粒。利用该方法合成的金刚石颗粒具有微米级尺寸,可用作研磨剂、抛光剂、形核剂等。但是合成的金刚石颗粒中仍含有少量的非晶碳,且合成颗粒的尺寸均匀性有待提高。为解决以上问题,本文中在反应不同阶段(初期、中期及末期)通入氧气,形成氧等离子体;研究氧等离子体对合成的金刚石颗粒形貌、尺寸、质量、纯度的影响,以及随氧等离子体添加阶段不同而产生的不同变化情况。结果表明,经氧等离子体处理的金刚石颗粒形貌略有改变,表面光滑度更好,且金刚石颗粒尺寸的一致性有所提高;经过激光粒度测试发现,金刚石颗粒的尺寸主要集中在25~29μm。添加氧等离子体有助于消除金刚石中的非晶碳,提高金刚石纯度;且在反应初期添加氧等离子体可最大程度提高金刚石颗粒质量。     

Oxidation of Styrene with Molecular Oxygen in Supercritical CO2

The oxidation of styrene with molecular oxygen catalyzed by PdCl2 CuCl2 has been investigated in supercritical CO2 with a batch reactor. The oxidative system of styrene contains four components at the beginning and seven components during the reaction. The critical temperature, critical pressure, and critical density at different conversions are determined by using a high-pressure view cell. The effect of phase behavior on the conversion and selectivity were studied. Experimental results showed that the critical parameters of the reaction mixture at fixed initial molar ratio changed with the conversion of reactant. The conversion of styrene reached maximum near the critical density of the reaction mixture. Product selectivity also varied with density of reaction mixture and could be tuned to some degree.     

反应挤出法合成S/B多嵌段共聚物的研究

在阴离子引发体系下 ,以双螺杆挤出机为反应器 ,采用丁二烯、苯乙烯混和单体加料方式 ,本体法一步合成了S B多嵌段共聚物 .考察了螺杆转速、进料速率以及不同丁苯配比对反应挤出合成PS及S B嵌段共聚物聚合转化率的影响 .用1 H NMR、IR、DMA、TEM等方法对S B嵌段共聚物进行了表征 ,结果表明共聚物由多个微小的丁二烯嵌段和少量无规段组成 .当丁二烯含量少至 15 %左右时 ,其嵌段可回缩成球状 ,粒径大约在 30～ 5 0nm .该材料的韧性随着共聚物中丁二烯含量的增加而逐渐提高 ,特别是断裂延伸率的提高尤为显著