Al_2O_3－SiO_2石油裂化催化剂上自由基空间分布的ESR成象

报道了用自己设计制作的电子自旋成象装置，对芳烃芳胺化合物在Ａｌ２Ｏ３－ＳｉＯ２催化剂表面酸中心所形成的正离子自由基进行二维ＥＳＲ成象研究．     

L波段三维ESR成像系统的研制(Ⅰ)——L波段ESR成像的磁场及三维梯度磁场系统

研究并实现了L波段电子自旋共振三维成像（3D-EPRI）专用的三维梯度磁场系统，主磁场及扫描磁场系统以及相应的驱动控制系统. 梯度场线圈采用在铜板上用电切割方法加工的 平板式线圈，避免了用铜导线绕制线圈体积较大的缺点，从而缩小了主磁场的体积和极间距 . 梯度场强度在三维方向上均达到200 mT/m，驱动电流为20 A. 三维空 间线性度均优于5％；线性区域大于直径42 mm的球形空间. 两磁极间距离为63 mm，可以容纳通常体积的L波段谐振腔. 主磁场和扫描场线圈固定在同一轭铁架上. 它们可分别产生1.6～ 96 mT和0.2～16 mT的线性变化磁场. 5组磁场线圈（包括主磁场， 扫描磁场和三维梯度磁场）分别由5台独立的恒流驱动电源控制驱动. 电源通过数据接口由计算机控制. 初步成像实 验证明本工作所建立的磁场和梯度磁场系统可以用于EPRI实验.     

基于ArcXML和Winsock搭建WebGIS技术的研究

本文分析了基于ArcXML和Winsock来搭建WebGIS的技术原理,在此基础上提出了实现方法,并通过流程图的形式详细描述相关功能实现的过程,最后总结了该技术的特点以及相关应用方向.     

Plate form three-dimensional gradient coils for L-band ESR imaging experiment

A set of plate form three-dimensional magnetic gradient coils was developed and used in electron spin resonance imaging (ESRI) experiment. The coils were processed with whole copper plates instead of wound with copper wires, which made its structure so compact that it was much thinner and smaller comparing to those traditionally used in ESRI. The coil set had a pie-like appearance of which the total thickness was only 14 mm and the outer diameter was 250 mm. The efficiency of the coils could be greater than 10 mT/m/A when distance between the two side-pieces was 63 mm. A maximum gradient strength of more than 200 mT/m could be obtained with driving current of about 20 A in each dimension coil. The spatial linearity was better than 5% in all three dimensions within the available spatial linearity area of larger than a sphere of 40 mm in diameter. The stability of the gradients strength could reach the level of 10(-5). An imaging resolution of better than 1 mm could be achieved with the coil set. Some preliminary practical imaging results show that the developed gradient coil set is suitable for L-band ESRI experiment of biological samples or even in vivo small animals.     

ESR imaging and FTIR study of thermally treated poly(acrylonitrile-butadiene-styrene) (ABS) containing a hindered amine stabilizer: Effect of polymer morphology, and butadiene and stabilizer content

Electron spin resonance imaging (ESRI) was applied to the study of thermal degradation at 393 K of poly(acrylonitrile-butadiene-styrene) (ABS) prepared by emulsion polymerization and containing 25% wt butadiene (ABS-25B). The polymer was doped with 1 or 2% wt Tinuvin 770 as the hindered amine stabilizer (HAS). The spatial distribution of the HAS-derived nitroxide radicals, obtained by 1D ESRI, was initially homogeneous, but became heterogeneous through sample depth with increasing treatment time, t. The spatial variation of ESR line shaping with sample depth was visualized by 2D spectral-spatial ESRI. ESR spectra along the sample depth, obtained by nondestructive (“virtual”) slicing of the 2D images, were used to deduce the relative intensity of nitroxide radicals present in two dynamically distinct sites; the sites were assigned to butadiene-rich (fast component) and SAN-rich domains (slow component), respectively. 1D and 2D ESRI allowed the determination of the extent of degradation within morphologically-distinct domains as a function of sample depth and treatment time. The results from the ESRI experiments were substantiated by attenuated total reflectance (ATR)-FTIR spectroscopy of the outer layer (500 μm thick) of the polymer. Both techniques indicated faster degradation of polymer samples that contained the higher HAS content, 2% wt. Comparison with the results obtained for a parallel study of ABS prepared by mass polymerization and containing 10% wt butadiene (ABS-10B) indicated clearly that the rate of degradation of the polymer prepared by emulsion polymerization (ABS-25B) is significantly reduced. This result can be explained by the formation of cross-linked “composite” networks during emulsion polymerization, which leads to greater thermal stability.     

Al2O3-SiO2石油裂化催化剂上自由基空间分布的ESR成象

报道了用自己设计制作的电子自旋成象装置,对芳烃芳胺化合物在Al₂O₃-SiO₂催化剂表面酸中心所形成的正离子自由基进行二维ESR成象研究.     

NOR and nitroxide-based HAS in accelerated photooxidation of carbon-chain polymers; Comparison with secondary HAS: An ESRI and ATR FTIR study

Understanding processes resulting in heterogeneous degradation in polymers is of extreme importance for improving their stabilization and minimizing negative impact of photooxidation on the material properties. We adopted modern physical techniques for studies of spatial distribution of intermediates and products of photodegradation during accelerated ageing of four commodity polymers, polypropylene (PP), polyethylene (PE), polystyrene (PS) and poly(ethylene-co-norbornene) (Topas^®, TP) stabilized with hindered amine stabilizer (HAS). Concentration profiles of nitroxides inside polymer plaques along the direction perpendicular to their surface were determined by electron spin resonance imaging (ESRI) as a function of the duration of the accelerated photooxidation. We present data characterizing stabilization activity of three alkoxyamine derivatives of HAS (Tinuvin^® NOR 123, Tinuvin^® NOR 371, Flamestab^® NOR 116), Chimasorb^® 119 structurally similar to Flamestab^® NOR 116, and nitroxide-based HAS Dastib^® 1045 and compare them with the data characterizing stabilization activity of the secondary HAS (>NH) Tinuvin^® 770. ESRI data are complemented by ATR FTIR spectroscopic detection of oxidation products on the surface and inside the plaques and by data characterizing diffusive optical transmittance of the polymer plaques in the spectral region 280-400 nm (terrestrial range of the solar UV radiation).