煤直接液化油中混合酚的分离研究

利用分子筛择形特点，对煤直接液化油中的混合酚实施高效分离。本研究选取间甲酚和对甲酚作为分离煤直接液化油馏分段混合酚的模型化合物，采用化学液相沉积法对HZSM-5吸附剂的孔口结构进行改变，分析分子筛硅铝比及颗粒粒径对模型化合物间甲酚和对甲酚吸附分离性能的影响，以获得高性能固相吸附剂，并将其应用于180-190℃馏分段混合酚分离。结果表明，当分子筛硅铝比为25、粒径为3-5 μm时，分子筛的孔口结构调节效果最优；当正硅酸乙酯的最小用量为0.2 mL/g时，固相吸附剂的吸附量为0.03 g/g，对甲酚选择性高于95%。由于外表面沉积物对吸附剂的孔口结构变化，导致对甲酚选择性的提高。进一步采用HZSM-5（1）吸附剂对真实煤直接液化油混合酚的分离中发现，苯酚和对甲酚的选择性均达到100%。     

电极/水溶液界面的SERS研究Ⅰ.Cu/1.0M的Na_2SO_4和NaCl溶液体系

电极／水溶液界面的ＳＥＲＳ研究Ⅰ．Ｃｕ／１．０Ｍ的Ｎａ２ＳＯ４和ＮａＣｌ溶液体系陈燕霞黄开启田中群（厦门大学化学系固体表面物理化学国家重点实验室物理化学研究所厦门３６１００５）ＳＥＲＳＳｔｕｄｉｅｓｏｆＥｌｅｃｔｒｏｄｅ／ＥｌｅｃｔｒｏｌｙｔｅＳｏ...     

第二届西安机器视觉与工业检测展览会隆重召开

2006年10月19日,由西安机器视觉研究发展中心和西安市技术市场管理办公室、西安市高新技术产业推进办公室主办,由西安光电子专业孵化器、西安光电子行业协会共同承办、西安高新区管委会经济贸易发展局支持的第二届西安机器视觉及工业检测展览会在西安光电园隆重召开.这是西安机器视觉及工业检测领域的一次盛会,也是西安乃至西北地区机器视觉方面的专业展览会.……     

Kinetic Studies of Electrochemical Oxidation of 1,3-Benzenedithiol

The electrochemical oxidation of 1, 3-benzenedithiol was investigated in a 0. 100 mol/L tetrabutylammonium perchlorate/acetonitrile electrolyte. The electrochemical techniques used were potential sweep, bulk electrolysis, rotating disc and the potential step method. The combination of the techniques yielded the number of electrons transferred per molecule, the reaction order, the transfer coefficient, the diffusion coefficient and concentration of dithiol anions, the standard heterogeneous rate constant as well as the formal potential and equilibrium constant of the preceeding dissociation reaction. This paper also illustrates the methods for studying the electrode kinetics of reactions which (a) involve a chemical reaction preceeding the electron-transfer process, (b) have insoluble polymer products, and (c) are totally irreversible.     

案例1:HCD1328(118)TSD线路板短路漏电的原因

一、样品描述 所送样品为型号为HCD1328(118)TSD的线路板,该批板有不同程度的短路漏电现象,而与之配套的显示板和芯片内依线显示正常,今委托单位要求分析该板短路漏电的原因。     

中国信息化趋势报告(五)加强我国政府信息资源开发利用的若干问题

1政府信息资源的界定 (一)政府信息资源 政府信息资源包括政府部门为履行管理国家行政事务的职责而采集、加工、使用的信息资源;政府部门在业务过程中产生和生成的信息资源;由政府投资建设的信息资源以及由政府部门直接管理的信息资源.     

Least squares approach in measurement-dependent filtering for selective medical images

An image-processing method called measurement-dependent filtering has been introduced to improve the SNR (signal-to-noise ratio) of selective images produced by various medical imaging systems. The basic algorithm involves the combination of the low-frequency information of the selective image with the high-frequency information of a nonselective image. A spatially variant control function modulates the amount of high frequency to be added at each point. A least-mean-square (LMS) control function formed from two basis images, namely the high-passed versions of the nonselective image (M(b)) and the selective image (S(b)), is introduced. The original algorithm is now viewed as a two-stage filtering method, including the low-pass filtering noise reduction and least squares filtering for the edge restoration. An appropriate linear transformation is used to convert the original basis images M(b) and S(b) into a new pair with orthogonal noise. This allows the implementation of the LMS and control function with practically obtainable a priori knowledge.     

Covalent attachment of phospholipid analogous polymers to modify a polymeric membrane surface: a novel approach

A novel method for the surface modification of a microporous polypropylene membrane by tethering phospholipid analogous polymers (PAPs) is given, which includes the photoinduced graft polymerization of N,N-dimethylaminoethyl methacrylate (DMAEMA) and the ring-opening reaction of grafted poly-(DMAEMA) with 2-alkyloxy-2-oxo-1,3,2-dioxaphospholanes. Five 2-alkyloxy-2-oxo-1,3,2-dioxaphospholanes, containing octyloxy, dodecyloxy, tetradecyloxy, hexadecyloxy, and octadecyloxy groups in the molecular structure, were used to fabricate the PAP-modified polypropylene membranes. The attenuated total reflectance FT-IR spectra of the original, poly(DMAEMA)-grafted, and PAP-modified membranes confirmed the chemical changes on the membrane surface. Scanning electron microscope pictures showed that, compared with the original membrane, the surface porosities ofpoly(DMAEMA)-grafted and PAP-modified membranes were somewhat reduced. Water contact angles measured by the sessile drop method on PAP-modified membranes were slightly lower than that on the original polypropylene membrane, but higher than those on poly(DMAEMA)-grafted membranes with the exception of octyloxy-containing PAP-modified membranes. However, BSA adsorption experiments indicated that the five PAP-modified membranes had a much better protein-resistant property than the original polypropylene membrane and the poly(DMAEMA)-grafted membranes. For hexadecyloxy- and octadecyloxy-containing PAP-modified membranes, almost no protein adsorption was observed when the grafting degree was above 6 wt %. It was also found that the platelet adhesion was remarkably suppressed on the PAP-modified membranes. All these results demonstrate that the described approach is an effective way to improve the surface biocompatibility for polymeric membranes.