Ordered porous films based on fluorinated polyimide derived from 2,2′-bis(3,4-dicarboxyphenyl) hexafluoropropane dianhydride and 3,3′-dimethyl-4,4′-diaminodiphenylmethane

One of fluorinated polyimides was synthesized from 2,2′-bis(3,4-dicarboxyphenyl) hexafluoropropane dianhydride (6FDA) and 3,3′-dimethyl-4,4′-diaminodiphenylmethane (DMMDA) by two-steps method, which had good solubility and hydrophilicity. 6FDA-DMMDA polyimide was dissolved in chloroform (CHCl₃) and cast on a glass substrate in a humid atmosphere. It was found that 6FDA-DMMDA/CHCl₃ solution was easy to form ordered porous structure at high concentration, and the reason was discussed in detail. In addition, the influences of solution concentration, the atmosphere humidity, were also tested.     

Protection of immobilized sulfhydryl groups against autooxidation by alterations in their microenvironment

Immobilized sulfhydryl groups were prepared by partial thiolation of NH₂-glass beads. The microenvironment of the immobilized SH groups was varied by different chemical modifications of neighboring NH₂ groups. Introduction of a strong charge in the surroundings of immobilized sulfhydryls results in their dramatic stabilization against autooxidation. This effect is due to the salting of O₂ from the surface microlayer of the thiolated beads.     

互通多孔碳/二氧化锰纳米复合材料的原位水热合成及电化学性能

以互通多孔碳（IPC）为载体，水热条件下在碳表面原位反应生成纳米结构的二氧化锰（MnO₂），制备互通多孔碳/二氧化锰纳米（IPC/MnO₂）复合电极材料. 采用扫描电镜（SEM），透射电镜（TEM），X射线衍射（XRD），热重分析（TGA）对其结构进行表征；采用循环伏安法、恒流充放电和交流阻抗对其电化学性能进行研究. 结果表明：生成的MnO₂均匀地负载在碳的表面，形成多层次结构，并且随着温度的升高IPC表面负载的MnO₂由纳米颗粒变为纳米片状结构；MnO₂纳米片具有典型的K-Birnessite 型晶体结构；复合物中MnO₂的含量约为34%（w）. 在100 ℃制备的IPC/MnO₂复合材料在三电极系统中最高比电容达到了411 F·g^-1；随着反应温度的升高,比容量先增长后基本保持不变. 以IPC/MnO₂为正极，活性炭（AC）为负极，1 mol·L^-1 Na₂SO₄溶液为电解液组装成IPC/MnO₂//AC 混合超级电容器，发现IPC/MnO₂电极的电容器其电位窗口从1 V扩展到1.8 V，容量可达86F·g^-1，且表现出良好的电容特性和大电流放电性能.     

聚偏氟乙烯微孔膜的亲水化改性及功能化研究进展

聚偏氟乙烯(PVDF)微孔膜的亲水化改性方法有物理共混、化学共聚、表面涂覆、表面化学处理、表面接枝等几种。其中物理共混和表面涂覆法比较成熟且已获得应用，而PVDF微孔膜的表面化学处理、等离子体或光引发改性技术以及环境敏感性等将成为PVDF微孔膜的改性和功能化研究的主要方向。     

互通多孔碳/二氧化锰纳米复合材料的原位水热合成及电化学性能

以互通多孔碳（IPC）为载体，水热条件下在碳表面原位反应生成纳米结构的二氧化锰（MnO₂），制备互通多孔碳/二氧化锰纳米（IPC/MnO₂）复合电极材料. 采用扫描电镜（SEM），透射电镜（TEM），X射线衍射（XRD），热重分析（TGA）对其结构进行表征；采用循环伏安法、恒流充放电和交流阻抗对其电化学性能进行研究. 结果表明：生成的MnO₂均匀地负载在碳的表面，形成多层次结构，并且随着温度的升高IPC表面负载的MnO₂由纳米颗粒变为纳米片状结构；MnO₂纳米片具有典型的K-Birnessite 型晶体结构；复合物中MnO₂的含量约为34%（w）. 在100 ℃制备的IPC/MnO₂复合材料在三电极系统中最高比电容达到了411 F·g^-1；随着反应温度的升高,比容量先增长后基本保持不变. 以IPC/MnO₂为正极，活性炭（AC）为负极，1 mol·L^-1 Na₂SO₄溶液为电解液组装成IPC/MnO₂//AC 混合超级电容器，发现IPC/MnO₂电极的电容器其电位窗口从1 V扩展到1.8 V，容量可达86F·g^-1，且表现出良好的电容特性和大电流放电性能.     

Rigid aromatic fractal polyamides

The preparation of rigid aromatic, highly branched polyamides is described. Owing to the method of preparation and the chosen ratio of difunctional to trifunctional monomers, these entities are highly porous and not dendrimeric in nature. They better conform with the fractal model and are therefore called fractal polyamides (FPs). The effects of variations in the polymerization procedure, in total monomer concentration, in the ratio of amine to carboxyl groups and in the duration of the polycondensation reaction are investigated. Some characterization was performed and the results are presented and briefly discussed.     

互通多孔碳/二氧化锰纳米复合材料的原位水热合成及电化学性能

以互通多孔碳（IPC）为载体，水热条件下在碳表面原位反应生成纳米结构的二氧化锰（MnO₂），制备互通多孔碳/二氧化锰纳米（IPC/MnO₂）复合电极材料. 采用扫描电镜（SEM），透射电镜（TEM），X射线衍射（XRD），热重分析（TGA）对其结构进行表征；采用循环伏安法、恒流充放电和交流阻抗对其电化学性能进行研究. 结果表明：生成的MnO₂均匀地负载在碳的表面，形成多层次结构，并且随着温度的升高IPC表面负载的MnO₂由纳米颗粒变为纳米片状结构；MnO₂纳米片具有典型的K-Birnessite 型晶体结构；复合物中MnO₂的含量约为34%（w）. 在100 ℃制备的IPC/MnO₂复合材料在三电极系统中最高比电容达到了411 F·g^-1；随着反应温度的升高,比容量先增长后基本保持不变. 以IPC/MnO₂为正极，活性炭（AC）为负极，1 mol·L^-1 Na₂SO₄溶液为电解液组装成IPC/MnO₂//AC 混合超级电容器，发现IPC/MnO₂电极的电容器其电位窗口从1 V扩展到1.8 V，容量可达86F·g^-1，且表现出良好的电容特性和大电流放电性能.     

Polarization Dependence of a Hydrophobized Electrode for Electrosynthesis of a Soluble Product

An equation for a polarization curve of a hydrophobized electrode is proposed for electrosynthesis of a soluble electroactive product in an inner-kinetic mode. The equation contains the concentration of the target product (TP) in an explicit form. The shape of the curve depends on the biquadratic root of the TP concentration and the square root of the ratio between exchange currents of the side and target reactions.     

Transport of monooleoylglycerol mediated by bile salt micelles across porous membranes

In order to study how the bile salts and lipids behave in the vicinity of microvillus, the transport properties of a sodium salt of deoxycholic acid (NaDC) and its mixture with monooleoylglycerol (MO) through artificial membranes were investigated in 0.15 M NaCl saline solution at 37°C.The hydrodynamic radius of MO-solubilized micelles was estimated to be approximately 17–20 Å from the transport study. The thermodynamically stable MO-NaDC mixed micelles formed above critical micelle concentration in the higher region of mole fraction of NaDC in the mixture (X _NaDC>ca. 0.6), can behave as a single species in transport process and freely pass through the porous membranes of both pore sizes, 0.01 m and 0.1 m.The permeabilities of MO-NaDC mixed micelles are large compared with those of pure NaDC micelles. MO molecules solubilized may probably enhance the interaction between MO and NaDC molecules by better contacting with the respective hydrophobic groups in a mixed micelle (the flexible structure of MO molecule enables it), and in this situation, the smaller micelles compared with those of pure NaDC must be more favorable.     

Self-avoiding walks on random fractal environments

Self-avoiding random walks (SAWs) are studied on several hierarchical lattices in a randomly disordered environment. An analytical method to determine whether their fractal dimensionD _saw is affected by disorder is introduced. Using this method, it is found that for some lattices,D _saw is unaffected by weak disorder; while for othersD _saw changes even for infinitestimal disorder. A weak disorder exponent is defined and calculated analytically [ measures the dependence of the variance in the partition function (or in the effective fugacity per step)vL on the end-to-end distance of the SAW,L]. For lattices which are stable against weak disorder (<0) a phase transition exists at a critical valuev=v ^* which separates weak- and strong-disorder phases. The geometrical properties which contribute to the value of are discussed.