红外光谱在线监控对二苯脲合成反应进程的研究

利用ReactIRTM4000实验室在线红外分析系统对脲和苯胺合成二苯脲反应进行在线监控,通过监测反应物脲(1 420 cm-1)和苯胺(1 270 cm-1)、中间产物苯基脲(1 339 cm-1)及产物二苯脲(1 312 cm-1)特征峰的变化,推断出反应体系中各组分浓度的变化,从而清楚地了解了该反应的进程。研究的结果证明脲和苯胺合成二苯脲的过程是脲和苯胺先生成中间产物苯基脲,苯基脲再和苯胺生成二苯脲。结果表明在线红外分析能够快速、简便、准确地确定出反应的最佳时间,从而达到对合成反应的进程进行控制的目的。     

光源稳定性对简并四波混频信噪比影响的实验研究

在碘蒸气中研究了染料激光稳定性对简并四波混频(DFWM)信噪比的影响。实验中采用多模Nd∶YAG激光器倍频的输出泵浦染料激光器(染料PM580溶于酒精)。在具有前向补偿分光系统和图像探测系统的帮助下,在常温常压条件下测得泵浦光在波长为554.013 nm时达到饱和光强为290 μJ。同时发现染料激光器的光稳定性(输出波长范围,光束质量和能量转换效率等)随使用时间,泵浦激光脉冲次数和能量的增加而逐渐减弱。另外通过对比发现在染料激光器输出不稳定时,光源单色性和指向性等指标的变化导致在同一泵浦强度不同时刻获得的DFWM信号强度相差很大,且DFWM信号信噪比低。染料激光器光源稳定性对DFWM信号影响的研究结果对物质的痕迹量探测以及无荧光物质光谱定标等方面的应用具有重要意义。     

激光感生碰撞能量转移实验

首次观察到Eu(6s6p)^P9/2至Sr(5s10s)^1So、准稳态翼为紫翼的激光感生碰撞能量转移实验现象,其荧光波长为458.42nm,峰值转移激光波长为459.75nm,并对其激发函数谱随温度和随转移激光能量改变进行实验研究,测量了激光感生碰撞能量转移谱的截面,证实了激光感生碰撞能量转移谱为非对称谱。     

多孔介质对流干燥外部传热传质的非平衡热力学理论

从非平衡热力学理论出发,以广义热力学力作为传质过程驱动势,建立了描述多孔介质恒速干燥阶段外部对流传热传质过程的热力学理论模型,并进行了数值计算,计算值与已有的实验数据吻合较好;同时,还将计算结果与传统的理论进行了比较,结果表明,非平衡热力学理论更能反映过程的物理本质。     

ADSORPTION BEHAVIOR OF AMINO ACIDS ON COPPER SURFACES

The major results of a series of our recent investigations on the adsorption of eight amino acids on Cu(001) and (111) surfaces are reviewed in the present paper. In all studied cases the molecules adsorb onto the surface in their anionic form. With the increase of the coverage three different 2D phases of the adsorbates, that is, the 2D lattice gas, intermediate, and solid phases, appear sequentially, although for few systems one or two of them do not appear. In both the 2D lattice gas and intermediate phases the molecules "stand" with their two oxygen "feet" on the surface and the intermolecular interactions are repulsive, although in the former they can diffuse frequently whereas in the latter they are discommensurate in one direction with the substrate. In the solid phase the molecules "lie" down on the surface to form commensurate superstructures. Adsorption of amino acids may often induce step faceting as well as bunching to form facets. Adsorption of L-lysine on Cu(001) may cause steps bunching to form facets with all the same chirality. Our preliminary results show that it is possible to manipulate individual molecules with the STM tip even at room temperature. These results may have applications in nano-materials, nano-technology, and very likely also in chiral separations or enantioselective heterogeneous catalysis.     

辣根过氧化氢酶电极的研究

以辣根过氧化氢酶修饰电极采用循环伏安法对环境污染物对对苯二酚进行了测定 ,对测定条件进行了探索 ,该电极在 p H7,H2 O2 浓度为 1 0μmol· L-1时对苯二酚具有良好的响应 ,其线性范围为 2 .0× 1 0 -5～ 2 .8× 1 0 -3mol·L-1,检测下限为 1 .0× 1 0 -6mol· L-1。电极的峰电流与扫描速度的平方根成正比 ,电极上的传质过程受扩散控制 ,对酶催化反应的动力学机制进行了探讨。     

一种具有高速选择性的技术—分了烙印

分子烙印技术作为一个新概念被提出来,虽然国外已有一部分人在这方面作出了一些研究,但国内这方面的报道却很少,本文从自组装方法和预聚合方法两种合成分子烙印聚合物的模型,烙印分子、功能性聚合物单体及聚合条件的选择,分子烙印聚合物的特点,应用展望等作了评述。     

Cs-Sr系统中激光感生非弹性碰撞过程的数值研究

利用已建立的四能级理论模型对提出的Cs Sr中的两个激光感生碰撞过程进行了数值计算 ,得到了碰撞跃迁几率随碰撞参数的变化关系及碰撞截面随转换激光失谐量的变化关系 ,并与三能级近似理论模型的计算结果进行了比较 .通过比较四能级理论与三能级近似理论模型的计算结果 ,进一步证实了理论的分析 :当 |ω_{2 1}|值与 |ω₄₃ |相近时 ,三能级理论的计算结果将存在着很大的误差 ,而四能级理论模型则适合于计算各种条件下的激光感生碰撞过程 .     

Conical bubble photoluminescence from rhodamine 6G in 1, 2-propanediol

A modified U-tube conical bubble sonoluminescence device is used to study the conical bubble photoluminescence. The spectra of conical bubble sonoluminescence at different concentrations of rhodamine 6G (Rh6G) solution in 1,2-propanediol have been measured. Results show that the sonoluminescence from the conical bubbles can directly excite Rh6G, which in turn can fluoresce. The light emission of this kind is referred to as conical bubble photoluminescence. The maximum of fluorescence spectral line intensity in the conical bubble photoluminescence has a red shift in relative to that of the standard photo-excited fluorescence, which is due to the higher self-absorption of Rh6G, and the spectral line of conical bubble photoluminescence is broadened in width compared with that of photo-excited fluorescence.     

一种含有手性联萘“铰链”单元的环芳分子的设计、合成及表征

基于联萘衍生物手性构型高度稳定以及联萘结构中2个萘平面的两面角可以在一定范围内张合的特点, 分别以光学活性的(R)和(S)-2,2'-二乙炔基-1,1'-联萘为模板, 设计了一种含有8个“铰链”结构单元的新的环芳分子¾—(R,R,R,R,R,R,R,R)-3和(S,S,S,S,S,S,S,S)-3. 其合成路线涉及间苯基连接桥的链接, 保护基的脱去和控制导入以及分子间偶合等步骤. 用MS, IR, UV-Vis, ¹H和¹³C NMR以及元素分析等技术对中间体和目标化合物进行了结构表征. 测定并比较了2个目标化合物的比旋光度[α]_D和圆二色(CD)性质. 在CH₂Cl₂溶液中, 两个异构体(R,R,R,R,R,R,R,R)-3和(S,S,S,S,S,S,S,S)-3的[α]_D²⁵值分别为－911.8和＋908.6, 并且它们的CD谱表现出对称的镜像特征．这些实验结果清楚地反映了它们之间的对映异构关系.