Submitted master thesis is by its character focused on development of polyaniline which would possess attributes typical for monolithic stationary phase. Developed polyaniline aims to be used in capillary liquid chromatography. Accompanying target of submitted master thesis is to provide solutions for variety of complications which follow the preparation of polyaniline in its desired form such as consistency in a form of solutions, gels and pastes, extremely fast polymerization reaction, limited solubility of cross-linking agents, solubility of monolithic polyaniline in polar mobile phases and insufficient bond of polyaniline to the inner wall of fused silica capillary tubing. Solutions for this complications are selection of ideal oxidation agent (ammonium persulfate), cross-linking agent (tris(4-aminophenyl)amine) and porogenic agent (methanol). Also, setting ideal ratio between oxidation agent, cross-linking agent and porogenic agent, heat treatment, choice of suitable mobile phase (tetrahydrofuran), adjustment of capillary wall using silanization agent (3-[3-(trimethoxysilyl)propyl]-aniline) and construction of equipment needed for quick filling of capillaries. Described development concluded in the preparation of solid polyaniline monolith which had a steady bond to the inner wall of fused...

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Self assembled monolayers (SAMs) are widely used for surface modification. Alkylsilane monolayers are one of the most widely deposited and studied SAMs. My work focuses on the preparation, patterning, and application of alkysilane monolayers. 3-aminopropyltriethoxysilane (APTES) is one of the most popular silanes used to make active surfaces for surface modification. To possibly improve the surface physical properties and increase options for processing this material, I prepared and studied a series of amino silane surfaces on silicon/silicon dioxide from APTES and two other related silanes by chemical vapor deposition (CVD). I also explored CVD of 3-mercaptopropyltrimethoxysilane on silicon and quartz. Several deposition conditions were investigated. Results show that properties of silane monolayers are quite consistent under different conditions. For monolayer patterning, I developed a new and extremely rapid technique, which we termed laser activation modification of semiconductor surfaces or LAMSS. This method consists of wetting a semiconductor surface with a reactive compound and then firing a highly focused nanosecond pulse of laser light through the transparent liquid onto the surface. The high peak power of the pulse at the surface activates the surface so that it reacts with the liquid with which it is in contact. I also developed a new application for monolayer patterning. I built a technologically viable platform for producing protein arrays on silicon that appears to meet all requirements for industrial application including automation, low cost, and high throughput. This method used microlens array (MA) patterning with a laser to pattern the surface, which was followed by protein deposition. Stencil lithography is a good patterning technique compatible with monolayer modification. Here, I added a new patterning method and accordingly present a simple, straightforward procedure for patterning silicon based on plasma oxidation through a stencil mask. We termed this method subsurface oxidation for micropatterning silicon (SOMS).

Le présent mémoire porte sur la synthèse et caractérisation de nouveaux matériaux dérivés de la polyaniline. Ces matériaux possèdent dans leur structure l'unité carbazole afin de remédier à des problèmes de solubilité que présentent la polyaniline et ces dérivés, sans pour autant modifier de façon significative la structure recherchée de la polyaniline. L'étude électrochimique de composés modèles a d'abord été effectuée afin de mieux comprendre le comportement électrochimique des polymères synthétisés. Cette approche est d'un grand intérêt dans la famille des polyanilines puisque leur comportement redox est relativement compliqué. Ainsi, trois composés modèles et deux polymères ont été étudiés de façon approfondie. L'étude électrochimique et spectroélectrochimique nous a permis de prédire les différents processus électrochimiques possible pouvant intervenir lors de l'oxydation de ces matériaux.

Continuous population growth and rapid industrial advancement and development have paved the way for ever increasing environmental pollution. At present, water pollution is a serious global issue that threatens environmental sustainability. The contamination of aquatic bodies with potentially toxic organic and inorganic substances are the result of world-wide anthropogenic activities. These pollutants can have detrimental health consequences on humans and ecosystems. Over the past decades, techniques such as chemical precipitation, ion-exchange, adsorption, membrane filtration, and electrocoagulation-flocculation have been developed and employed for the treatment of drinking and wastewater. Among the currently available techniques, pollutant removal by adsorption is most promising due to its cost-effectiveness, simplicity in operation, environmental friendliness, and abundance of adsorbents. This study emphasized the utilization of biochar (BC), after appropriate surface modification, for the removal of potentially toxic contaminants. In the first study, a base activated biochar was synthesized by treating the biochar with potassium hydroxide (KOH) at 700 ℃ in a muffle furnace for 1 h. The resulting high surface area biochar (KOHBC) was used for the removal of Cr(VI), Pb(II) and Cd(II). In the second study, a biochar-supported polyaniline hybrid was synthesized for aqueous chromium and nitrate adsorption. Introduction of amine and imine groups to the biochar facilitated the removal of these contaminants. In the final study, a composite containing Fe-Ti oxide/biochar (Fe2TiO5/BC) was synthesized for sorptive removal of metal cations, oxy anions, inorganics, and organic contaminants from aqueous solutions. Additionally, this composite was used as a photocatalyst towards aqueous methylene blue (MB) degradation. The surface chemistry and composition of these adsorbents were examined by PZC SEM, TEM, XPS, FTIR, TGA, elemental analysis, and surface area measurements.

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