Polymeric microstructure arrays consequence of Marangoni flow-induced water droplets

This paper describes a cost-effective approach to fabricate intricate arrays of polydimethylsiloxane (PDMS) and polymeric microstructures based on porous polystyrene (PS) films generated from arrays of water droplets. To start, a thin layer of ethanol film is exposed to a humid air flow. Upon the evaporation of ethanol and simultaneous condensation of water as the ethanol phase recedes, a Marangoni flow causes the flow of liquid from the ethanol phase into water fingers emerged along the receding contact line, which finally detach to form ordered water droplet arrays behind the receding contact line. The water droplet arrays are subsequently used as templates to generate porous PS films. The porous PS films are then used as sacrificial layers and masters to fabricate various arrays of PDMS dots and PDMS stamps with posts, respectively. The PDMS stamps containing various microstructures are further utilized to create polymer rings, PDMS dots, porous PDMS films, and PDMS aperture rings, and for contact printing of patterns of self-assembled monolayers.     

Spectral shift of a twisted electromagnetic Gaussian Schell-model beam focused by a thin lens

Spectral changes of a twisted electromagnetic Gaussian Schell-model (EGSM) beam focused by a thin lens are investigated by using a tensor method. It is shown that the spectral shift is mainly determined by the degree of polarization, twist phase and correlation coefficients of the initial beam. Generically the blue shift occurs at on-axis points, while the red shift can occur at off-axis points.     

富勒烯[60]的光化学反应研究

从光物理出发,综述了近几年富勒烯「６０」的光化学反应研究进展。Ｃ６０能发生诸多的光化学反应：（１）光氧化;（２）光氢化还原;（３）「２＋２」光环化加成;（４）与叔胺的光加成;（５）与氨基酸的光加成;（６）与金属有机化合物的光加成。     

三价铬与丙二酸形成的配合物的热解过程研究

利用热重分析及原位红外光谱等方法，定性、定量地研究了三价铬和丙二酸形成的配合物［Ｃｒ（Ｃ３Ｈ２Ｏ４）（Ｈ２Ｏ）］［Ｃｒ（Ｃ３Ｈ２Ｏ４）２（Ｈ２Ｏ）２］·４Ｈ２Ｏ的热解过程，提出了室温至４００℃下的详细热解途径．基于多种实验结果，分析了螯合物中六员环的化学键断裂方式，并由配合物的快原子轰击质谱（ＦＡＢ－ＭＳ）加以佐证．     

Simultaneous determination of uric acid, xanthine and hypoxanthine with an electrochemically pretreated carbon paste electrode

A simple method is presented for the simultaneous differential pulse voltammetric determination of uric acid, xanthine and hypoxanthine. It is based on the improved current responses of the three analytes at carbon paste electrodes polarized in a dilute alkaline medium (0.002 mol/l NaOH, 0.1 mol/l NaClO₄) at 1.3 V vs. SCE for a short time. Compared with the methods reported in the literature, this procedure has a much wider linear range (2 to 3 orders of magnitude in concentration), lower detection limits (5 to 10 g l^–1) and less interference by ascorbic acid. The electrochemical responses were found to be dependent on the pre-anodization potential and the time imposed on the electrodes as well as on the alkalinity of the supporting electrolyte. The proposed procedure was used to determine uric acid, xanthine and hypoxanthine in human urine without any preliminary treatment.