Membrane processes can cover a wide range of separation problems [with a specific membrane (membrane structure) required for every problem]. Thus, there are membranes available that differ in their structure and consequently in the functionality. Therefore membrane characterization is necessary to ascertain, which membrane may be used for a certain separation. Membranes of pore size ranging from 100nm to 1μm with a uniform pore size are very important in membrane technology. An optimum performance is achieved when the membrane is as thin as possible having a uniform pore size. Here in this thesis, membranes were synthesized by particle assisted wetting using mono-layers of silica colloids as templates for pores along with polymerizable organic liquids on water surface. The pore size reflects the original shape of the particles. Thus it is possible to tune the pore size by varying the particle size. This method is effective to control pore sizes of membranes by choosing silica particles of suitable size. This approach gives a porous structure that is very thin, but unfortunately limited in mechanical stability. Thus there is a need for support which is robust and can withstand the various mechanical stresses. A small change in the membrane or defect in the layered structure during the membrane formation can have drastic effect on the assembly. Lateral homogeneity of the layer generated by the particle assisted wetting can be judged by examination of its reflectivity, but once it is transferred on any solid support this option is no more. So a method is needed to detect the cracks or the inhomogenity of the membrane which can be detected even after the transfer. To tackle this problem a very simple and novel technique for characterizing the membrane by fluorescence labeling and optical inspection was developed in this thesis. The idea was to add a fluorescent dye which is poorly water soluble to the spreading solution comprising of the particles and the monomer. If the dye survived the photo-cross linking, then it would be embedded in the cross-linked polymer and would serve as a marker. Defects and inhomogenity would show up as cracks and spots. By the method that we have developed, we can detect our membrane from the support and spot defects.

Membrane processes can cover a wide range of separation problems [with a specific membrane (membrane structure) required for every problem]. Thus, there are membranes available that differ in their structure and consequently in the functionality. Therefore membrane characterization is necessary to ascertain, which membrane may be used for a certain separation. Membranes of pore size ranging from 100nm to 1μm with a uniform pore size are very important in membrane technology. An optimum performance is achieved when the membrane is as thin as possible having a uniform pore size. Here in this thesis, membranes were synthesized by particle assisted wetting using mono-layers of silica colloids as templates for pores along with polymerizable organic liquids on water surface. The pore size reflects the original shape of the particles. Thus it is possible to tune the pore size by varying the particle size. This method is effective to control pore sizes of membranes by choosing silica particles of suitable size. This approach gives a porous structure that is very thin, but unfortunately limited in mechanical stability. Thus there is a need for support which is robust and can withstand the various mechanical stresses. A small change in the membrane or defect in the layered structure during the membrane formation can have drastic effect on the assembly. Lateral homogeneity of the layer generated by the particle assisted wetting can be judged by examination of its reflectivity, but once it is transferred on any solid support this option is no more. So a method is needed to detect the cracks or the inhomogenity of the membrane which can be detected even after the transfer. To tackle this problem a very simple and novel technique for characterizing the membrane by fluorescence labeling and optical inspection was developed in this thesis. The idea was to add a fluorescent dye which is poorly water soluble to the spreading solution comprising of the particles and the monomer. If the dye survived the photo-cross linking, then it would be embedded in the cross-linked polymer and would serve as a marker. Defects and inhomogenity would show up as cracks and spots. By the method that we have developed, we can detect our membrane from the support and spot defects.

Zeolites are microporous hydrated aluminosilicate crystals containing alkali and/or alkali earth metal cations in their frameworks. Due to their molecular size pores, they can separate molecules according to their size and shape. Zeolites are mostly used in ion exchange, adsorption processes and catalytic applications. The hydrophilic/hydrophobic character of zeolites also makes them favorable materials for adsorption based separations. Recently the potential of zeolite/ceramic composite membranes have been shown in the separation of liquid and gas mixtures. Self-supported zeolite membranes with asymmetric structure can be an alternative to the composite zeolite membranes. Because asymmetric structure may eliminate the problems originated from the differences in thermal expansion coefficients of zeolites and ceramics. In this study tubular zeolite A membranes were prepared on binderless zeolite A supports. The supports were perepared by hydrothermal conversion of amorphous aluminosilicate tubes into zeolite A. The amorphous aluminosilicate powder, which was obtained by filtering the homogenous hydrogel with a composition of 2.5Na2O:1Al2O3:1.7SiO2:150H2O, was mixed with an organic binder (HEC-Hydroxyethyl Cellulose) and water to obtain the paste. The paste was then extruded through a home-made extruder into bars and tubes. These extrudates were dried at room temperature for 24 hours, calcined at 600oC for 2 hours to remove organic binder and finally synthesized at 80oC for 72 hours in hydrothermal conditions to convert amorphous aluminosilicate to zeolite. The effect of composition of the synthesis solution on the crystallinity and morphology of zeolite A tubes and bars were investigated. The crystallization field of zeolite A bars has been established and shown on a ternary phase diagram. Tubes were mechanically stable, typically had a crystallinity over 90% and a macroporosity of 35%. The tubes were composed of highly intergrown crystals of zeolite A. The average particle size was 3.5 &micro / m. The asymmetric membranes were synthesized by growing zeolite A films on binderless zeolite A supports with a geometry of disk, bar and tube. Continuous zeolite A films can only be obtained when the supports were saturated with water prior to synthesis. The film thicknesses were approximately 5 &micro / m on disks and approximately 10 &micro / m on tubes. A method was proposed to prepare self-supported tubular zeolite A membranes in this study.

No description available.

For many years, inflatable structures and membrane enclosed structures have proved useful for a variety of purposes, such as athletic pavilions, exhibition spaces, coliseums, and kiosks. More recently, structures that combine highly pressurized inflatable arch members with light fabric membrane coverings have been considered for use as a variation of such structural systems. The United States Army has begun to investigate pressurized arch-supported membrane shelters that would be large, lightweight, and easily erected in a short amount of time. These shelters are proposed for a variety of purposes, including aircraft hangars, vehicle maintenance shelters, and medical aid stations. The specific contribution of this study was the creation and testing of scale models to obtain a better understanding of how these structures behave under wind and snow loading conditions. Three models were constructed, one at a scale of 1:100 and two at a scale of 1:50. The 1:100 scale model represented a proposed prototypical structure 200 ft long, 75 ft wide, and 50 ft tall, with multiple arches. Of the 1:50 scale models, one model represented a structure with the same dimensions as the 1:100 scale model and the other represented a single arch from one of the proposed prototypical structures. Both of the full structural models were wind and snow load tested. The single arch model was tested under full and partial snow loading. Data from the testing were collected, tabulated, and evaluated. The experimental results are discussed, conclusions are drawn, and recommendations for further research are presented. / Master of Science

No description available.

Les membranes cellulaires naturelles sont des structures complexes et posent de nombreux problèmes lorsqu'elles sont étudiées dans leur forme native. Par conséquent, des systèmes modèles lipidiques plus simples sont souhaitables pour étudier les composants des membranes cellulaires et leur interaction avec les molécules biologiques. Immobiliser ces modèles lipidiques sur des surfaces solides métalliques, pour former des bicouches biomimétiques supportées (SLB pour Supported Lipid Bilayer en anglais), est encore plus avantageux grâce leur adaptabilité à de nombreuses techniques de caractérisation de surface, telles que la microscopie de force atomique (AFM), la spectroscopie de résonance des plasmons de surface (SPR), l’électrochimie et les spectroscopies vibrationnelles (IR, Raman). Former ces bicouches lipidiques supportées par fusion des vésicules a toujours été la technique la plus adaptée vue sa simplicité et son efficacité. Cependant, cette technique exige des conditions expérimentales critiques comme la nécessité de surfaces planes lisses et hydrophiles (mica, verre…), des vésicules à base de phospholipides zwitterioniques en phase fluide, une concentration élevée en lipides, et une longue durée d’incubation (>1h). Dans cette thèse, nous visons à développer une nouvelle méthode simple, rapide et polyvalente permettant de former une large gamme de bicouches biomimétiques supportées, de type zwitterionique et anionique, en phase gel et fluide sur un substrat d’or. Cette nouvelle approche consiste en l’utilisation des réactions d’appariement ionique générées par un système rédox confiné en surface pour induire l’assemblage de phospholipides et former la bicouche lipidique. Le premier objectif de cette thèse est d’étudier le comportement électrochimique d’une monocouche auto-assemblée de ferrocényldodécanethiolates (FcC12SAu) en présence de molécules amphiphiles avec des groupes anioniques de types carboxyle (sel d’acide gras) et phosphate (groupes qu’on trouve dans les phospholipides) et une simple chaîne hydrocarbonée. Dans le même contexte, nous viserons également l’utilisation des réactions d’appariement ionique pour induire l’assemblage des surfactants n-alkyl carboxylate et n-alkyl phosphate à l’interface SAM/électrolyte. Le second objectif de ce travail de thèse consiste en l’utilisation du système rédox confiné en surface pour déclencher par appariement ionique l’assemblage des phospholipides (molécules amphiphiles à double chaînes hydrocarbonées) pour former des bicouches biomimétiques supportées sur une surface d’or, à partir de vésicules unilamellaires, à température ambiante et en quelques minutes. La couverture de surface en ferrocènes et l’hydrophobicité/hydrophilicité de la surface seront altérées par la suite pour investiguer l’effet sur la formation des bicouches lipidiques supportées. / Natural cell membranes are complex structures and may present many problems when studied in their native form. It is therefore desirable to have simpler lipid bilayer systems to study the components of cell membranes and their interaction with biological molecules. Immobilizing these lipid membranes on metallic solid surfaces, to form Supported Lipid Bilayers (SLB), is more advantageous due to the integrity with a wide range of surface-sensitive characterization techniques, such as atomic force microscopy (AFM), surface plasmon resonance spectroscopy (SPR), electrochemistry and vibrational spectroscopies (IR, Raman). The preparation of SLBs by vesicle fusion has always been the most suitable technique due to its simplicity and efficiency, but it requires critical experimental conditions such as the need for smooth and hydrophilic flat surfaces (mica, glass...), vesicles based on zwitterionic phospholipids in fluid phase, high lipid concentration, and lengthy SLB preparation times (>1h). In this thesis, we aim to develop a new simple, fast, and versatile method to form a wide range of supported biomimetic bilayers using zwitterionic and anionic phospholipid vesicles in gel and fluid phase on a gold substrate. This new approach consists in the use of ionic pairing reactions generated by a surface-confined redox system to induce the assembly of phospholipids and form the lipid bilayer. The first part of this thesis focuses on studying the electrochemical behavior of a self-assembled monolayer of ferrocenyldodecanethiolates (FcC12SAu) in the presence of amphiphilic molecules containing a carboxyl (fatty acid salt) and phosphate anionic group and a single hydrocarbon chain. This part will also focus on the use of ion-pairing reactions to induce the assembly of n-alkyl carboxylate and n-alkyl phosphate surfactants at the SAM/electrolyte interface. The second and main objective of this thesis work was subsequently devoted to the use of the surface-confined redox system to trigger by ion-pairing the assembly of phospholipids (amphiphilic molecules with double hydrocarbon chains) to form biomimetic bilayers supported on a gold surface from unilamellar vesicles at room temperature and within minutes. The surface coverage of ferrocenes and the hydrophobicity/hydrophilicity of the surface will be altered later to investigate the effect on the formation of supported lipid bilayers.