新型膜分离过程──膜分相技术及应用

在简要介绍膜分离机理的同时，重点介绍了膜分离技术的新进展—膜分相的原理、操作特点。通过膜分相应用实例与其它膜分离技术的比较和分析，展示了该技术在化工工业生产中的应用前景．

膜分相在含油废水处理中的应用研究

一、前言来自化工厂、炼油厂、机加工车间、油库、车库、油轮等等的含油废水,严重地污染着人类生活的环境。随着海洋法、环境保护法的实施,含油废水的处理成为日益迫切的任务。人们都在努力寻找简便、有效而经济的油水分离方法。这些年来,研究了许多新技术进行油水分离,以便使废水中的含油量达到排放标准。

用激光片光源照相法显示膜分相动态纯油层厚度

本项研究将脉冲激光片光源照相技术应用于膜分相动态纯油层的测定中。经过理论分析和测量系统设计，实现了膜分相过程中分相膜表面附近动态纯油层的显示和测定。

用膜分相技术从含油乳化液中分离油

本实验研制了适合于油/水乳化液分离的硅胶橡微孔膜,并对其配方和成膜条件进行了实验确定。同时对油/水乳液分散体系进行了运转,考察了油/水分离过程中对透油速度的各种影响因素。实验结果表明,油/水乳化液中乳化剂的不同、乳化液种类、乳化剂浓度、油的含量、压力和温度都影响透油速度。在操作压力下运转,透过的油中含水量一般在60ppm 左右。

用脉冲红宝石激光全息照相法测量膜分相动态纯水层厚度

本项研究将脉冲激光全息照相方法应用于膜分相动态纯水层厚度的测定中。通过高分辩率全息照相系统设计和大量的实验研究，成功地测量出膜分相过程中分相膜表面附近粒径为１～２μｍ的油珠分布图象以及动态纯水层厚度。

分相膜的结构及它的分相性能

本文用SEM 方法研究两种亲水膜的结构;用激光全息照相法测定亲水膜表面的纯水层厚度(t),还试验了这两种膜的除油效果。结果表明:分相膜的结构对纯水层厚度(t)和除油效果有影响,这对深入进行膜分相的机理研究和应用研究有重要意义。

Isolation of Plasma and Thylakoid Membranes from the Heterocystous Cyanobacterium Anabaena sp. PCC 7120

利用水溶性多聚体双相法分离蓝细菌Anabaenasp .PCC 712 0质膜和类囊体膜两种膜系统。吸收光谱分析表明 ,质膜相和类囊体膜相的主要色素分别为类胡萝卜素和叶绿素。SDS_凝胶电泳显示这两种膜系统蛋白组成有很大差别。这种分离方法容易操作 ,对研究蓝细菌的膜蛋白和膜脂非常有用。

Fluorescence Study on The Interaction Between Cisplatinand Erythrocyte Membrane Proteins

The interaction between cisplatin and erythrocyte membrane proteins was studied based on the quenching effect of cisplatin on the intrinsic fluorescence of proteins.A concentration-dependent quenching effect was observed.The presence of chloride and sulphate weakens the effect significantly.A pH-dependence was also noted with a stronger effect in acidic solution. The nature of the interaction is considered to be platinum-thiol group binding according to the effect of cisplatin on the fluorescence of FMA labeled membrane. The mechanism of the cisplatin-protein interactions was discussed based on the effect of coexisting anion

Influence of Poly（methyl metacrylate） Addition on Resistive Switching Performance of P3HT/P（VDF-TrFE） Blend Films

Organic semiconducting/ferroelectric blend films attracted much attention due to their electrical bistability and rectification properties and thereof the potential in resistive memory devices. Blend films were usually deposited from solution, during which phase separation oc- curred, resulting in discrete semiconducting phase whose electrical property was modulated by surrounding ferroelectric phase. However, phase separation resulted in rough surface and thus large leakage current. To further improve electrical properties of such blend films, poly（methyl metacrylate） （PMMA） was introduced as additive into P3HT/P（VDF-TrFE） semiconducting/ferroelectric blend films in this work. It indicated that small amount of PMMA addition could effectively enhance the electrical stability to both large electrical stress and electrical fatigue and further improve retention performance. Overmuch PMMA addition tended to result in the loss of resistive switching property. A model on the configuration of three components was also put forward to well understand our experimental observations.

Effects of F127 on Properties of PVB/F127 Blend Hollow Fiber Membrane via Thermally Induced Phase Separation

Hydrophilic poly(vinyl butyral)(PVB) /Pluronic F127(F127) blend hollow fiber membranes were prepared via thermally induced phase separation(TIPS) ,and the effects of blend composition on the performance of hydrophilic PVB/F127 blend hollow fiber membrane were investigated.The addition of F127 to PVB/polyethylene glycol(PEG) system decreases the cloud point temperature,while the cloud point temperature increases slightly with the addition of F127 to 20%(by mass) PVB/F127/PEG200 system when the concentration of F127 is not higher than 5%(by mass) .Light scattering results show that the initial inter-phase periodic distance formed from the phase separation of 20%(by mass) PVB/F127/PEG200 system decreases with the addition of F127,so does the growth rate during cooling process.The blend hollow fiber membrane prepared at air-gap 5mm,of which the water permeability increases and the rejection changes little with the increase of F127 concentration.For the membrane prepared at zero air-gap,both water permeability and rejection of the PVB/F127 blend membrane are greater than those of PVB membrane,while the tensile strength changes little.Elementary analysis shows that most F127 in the polymer solution can firmly exist in the polymer matrix,increasing the hydrophilicity of the blend membrane prepared at air-gap of 5mm.

Effects of Additives and Coagulant Temperature on Fabrication of High Performance PVDF/Pluronic F127 Blend Hollow Fiber Membranes via Nonsolvent Induced Phase Separation

Poly（vinylidene fluoride） （PVDF） has become one of the most popular materials for membrane preparation via nonsolvent induced phase separation （NIPS） process. In this study, an amphiphilic block copolymer, Pluronic F127, has been used as both a pore-former and a surface-modifier in the fabrication of PVDF hollow fibermembranes to enhance the membrane permeability and hydrophilicity. The effects of 2nd additive and coagulant temperature on the formation of PVDF/Pluronic F 127 membranes have also been investigated. The as-spun hollow fibers were characterized in terms of cross-sectional morphology, pure water permeation （PWP）, relative molecular mass cut-off （MWCO）, membrane chemistry, and hydrolphilicity. It was obsered that the addition of Pluronic F 127 significantly increased the PWP of as-spun fibers, while the membrane contact angle was reduced. However, the size of macrovoids in the membranes was undesirably large. The addition of a 2nd additive, including lithium chloride （LiC1） and water, or an increase in coagulant temperature was found to effectively suppress the macrovoid for- mation in the Pluronic-containing membranes. In addition, the use of LiC1 as a 2nd additive also further enhanced the PWP and hydrophilicity of the membranes, while the surface pore size became smaller. PVDF hollow fiber with a PWP as high as 2330 L·m-2·h-1·MPa-1, a MWCO of 53000 and＇a contact angle of 71 o was successfully fabricated with 3% （by mass） of Pluronic F127 and 3% （by mass） of LiC1 at a coagulant temperature of 25 ℃, which shows better performance as compared with most of PVDF hollow fiber membranes made by NIPS method.

Separation Efficiency of Thin-film Evaporators

The recovery of contaminants and useful substances from liquid wastes, thepurification of production effluents and the separation of thermally instable mixtures are some ofthe multivarious applications of thin-film distillers in many processes of the chemical and alliedindustries and of the food industries. In a study carried out in pilot plants with distillation testsystems there was found a good agreement between the experimental separation results and thoseobtained by computing with a theorectical model; the latter is based on the assumption of phaseequilibrium between the vapour formed on an infinitely small element of area in a liquid film of anygiven concentric periphery of the vertically arranged evaporator. These tests were perfomed undervarious phase loads.

Relative Molecular Orientations in Organic Optoelectronic Films Probed via Polarization-Selected UV/IR Mixed Frequency Ultrafast Spectroscopy

Molecular packing patterns are crucial factors determining electron/energy transfer processes that are critical for the optoelectronic properties of organic thin film devices.Herein,the polarization-selective ultraviolet/infrared(UV/IR)mixed frequency ultrafast spectroscopy is applied to investigate the relative molecular orientations in two organic thin films of 7-(diethylamino)coumarin-3-carboxylic acid(DEAC)and perylene.The signal anisotropy changes caused by intermolecular energy/electron transfers are utilized to calculate the cross angles between the electronic transition dipole moment of the donor and the vibrational transition dipole moments of the acceptor,yielding the relative orientation between two adjacent molecules.Using this method,the relative orientation angle in DEAC film is determined to be 53.4°,close to 60°of its single crystalline structure,and that of the perylene film is determined to be 6.2°,also close to-0.2°of its single crystalline structure.Besides experimental uncertainties,the small difference between the angles determined by this method and those of single crystals also results from the fact that the thin film samples are polycrystalline where some of the molecules are amorphous.

Synergistic action of non-solvent induced phase separation in preparation of poly(vinyl butyral) hollow fiber membrane via thermally induced phase separation

A systematic study of air gap distance effects on the structure and properties of poly(vinyl butyral)hollow fiber membrane via thermally induced phase separation(TIPS)has been carried out.The results show that the hollow fiber membrane prepared at air gap zero has no skin layer; the pore size near the outer surface is larger than that near the inner surface; and the special pore channel-like structure near the outer surface is formed,which is quite different with the typical sponge-like structure caused by TIPS and the finger-like structure caused by non-solvent induced phase separation(NIPS),because of the synergistic action of non-solvent induced phase separation at air gap zero.The pore size gradually decreases from outer surface layer to the intermediate layer,but increases gradually from intermediate layer to the inner surface layer.With the increase of air gap distance,the pore size near the outer surface gets smaller and a dense skin layer is formed,and the pore size gradually increases from the outer surface layer to the inner surface layer.Water permeability of the hollow fiber membrane decreases with air gap distance,the water permeability decreases sharply from 45.50×10-7 to 4.52×10-7 m3/(m2·s·kPa)as air gap increases from 0 to 10 mm at take-up speed of 0.236 m/s,further decreases from 4.52×10-7 to 1.00×10-8 m3/(m2·s·kPa)as the air gap increases from 10 to 40 mm.Both the breaking strength and the elongation increase with the increase of air gap distance.The breaking strength increases from 2.25 MPa to 4.19 MPa and the elongation increases from 33.9% to 132.6% as air gap increases from 0 mm to 40 mm at take-up speed 0.236 m/s.

Tunneling Electron Induced Fluorescence from Single Porphyrin Molecules Decoupled by Striped-Phase Octanethiol Self-assembled Monolayer

We investigate tunneling electron induced luminescence from isolated single porphyrin molecules that are decoupled by striped-phase self-assembled monolayer of octanethiol from the underneath Au（111） substrate. Intrinsic single-molecule electroluminescence has been realized by such decoupling at both bias polarities. The photon emission intensity acquired from the molecular lobe is found stronger than that from the molecular center. These re- sults provide useful information on the understanding of electroluminescent behavior and mechanism in molecular tunnel junctions.

Formation of Polyethersulfone Film with Regular Microporous Structure by Water Vapor Induced Phase Separation

Polyethersulfone(PES)film with regular microporous structure was formed using dichloromethane as the solvent via water vapor induced phase separation(VIPS).The effects of solution concentration,atmospheric humidity and temperature,as well as molecular weight of PES on the surface morphology of the polymer film were investigated.The surface morphology characterized by SEM showed that the pore size reduced as the solution concentration increased.There was an optimum range of relative humidity for the formation of regular pore structure, which was from 60%to 90%at concentration of 20 g·L-1 and 20°C.With the atmospheric temperature varied from 20 to 30°C,the pore became larger and the space between pores increased.The pore size in the PES film with low molecular weight was smaller than that with high molecular weight.

Novel nanofiltration membranes with tunable permselectivity by polymer mediated phase separation in polyamide selective layer

Microstructure in selective layer has played a decisive role in permselectivity of nanofiltration(NF) membranes,and nanomaterials were well-known additives that had been applied to mediate the microstructure and permeability of polyamide NF membranes. However, nanoadditives generally displayed a poor dispersion in membranes or in fabrication process. To solve this problem, we showed an interesting concept that novel NF membranes with hybrid selective layer consisting of flexible polyisobutylene(PIB) and rigid polyamide could be fabricated from well-defined interfacial polymerization. The hydrophobic polymer mediated phase separation and microdomains formation in polyamide layer were found. The immiscibility between the rigid polyamide and flexible PIB as well as the resultant interface effect was interpreted as the reason for the polymer enhanced permselectivity, which was similar with the well-known thin film nanocomposite(TFN) membranes that nanoparticles incorporated contributed significantly to membrane permeability and rejection performance.Our results have demonstrated that novel NF membranes with enhanced performance can be prepared from immiscible polymers, which is a new area that has not been extensively studied before.

Interaction of Egg-Sphingomyelin with DOPC in Langmuir Monolayers

Lipid rafts are a dynamic microdomain structure found in recent years, enriched in sphin- golipids, cholesterol and particular proteins. The change of structure and function of lipid rafts could result in many diseases. In this work, the monolayer miscibility behavior of mixed systems of Egg-Sphingomyelin （ESM） with 1, 2-dioleoyl-sn-glycero-3-phosphocholine was in- vestigated in terms of mean surface area per molecule and excess molecular area AAex at certain surface pressure, surface pressure and excess surface pressure Arcex at certain mean molecular area. The stability and compressibility of the mixed monolayers was assessed by the parameters of surface excess Gibbs free energy AGex, excess Helmholtz energy AHex and elasticity. Thermodynamic analysis indicates AAex and ATrex in the binary systems with positive deviations from the ideal behavior, suggesting repulsive interaction. The max- imum of AGex and AHex was at the molar fraction of ESM of 0.6, demonstrating the mixed monolayer was more unstable. The repulsive interaction induced phase separation in the monolayer.

Homogenization of a Class of Nonlinear Variational Inequalities with Applications in Fluid Film Flow

The authors consider the homogenization of a class of nonlinear variational inequalities,which include rapid oscillations with respect to a parameter.The homogenization of the corresponding class of differential equations is also studied.The results are applied to some models for the pressure in a thin fluid film fluid between two surfaces which are in relative motion.This is an important problem in the lubrication theory.In particular,the analysis includes the effects of surface roughness on both faces and the phenomenon of cavitation.Moreover,the fluid can be modeled as Newtonian or non-Newtonian by using a Rabinowitsch fluid model.

Correlation between the molecular structure and transcis isomerization characteristics of azobenzenes

Photochemical and thermal isomerization of various azobenzenes was systematically investigated to understand the correlation between the molecular structure and trans → cis isomerization characteristics of azobenzenes. A blue shift in π-π absorption band of ortho-alkylated azobenzenes （1o and 2o） was observed together with a reduction in molar extinction coefficient （e） in comparison with both meta-alkylated azobenzenes （4m and 5m） and 7p lacking the meta and ortho substituents. For orthoalkylated azobenzene, photochemical trans-to-cis isomerization and thermal back cis-to-trans isomerization in solution oc- curred slowly when compared with 4m, 5m and 7p. The half-life time of the cis form of 20 was found to be 380 h, which is about 8-50 times longer than those of comparable 4m, 5m （43-13 h） and 7p （7 h）. Furthermore, comparison of the molecular structure and isomerization characteristics of azobenzene thiol （20 and 5m） self-assembled monolayers on flat gold surfaces indicates that the trans-to-cis photoconversion in monolayer systems is influenced by steric hindrance and strong intermoleculax interaction between azobenzene units.