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As the Worlds energy demand is increasing we need more of our energy to be generated from resources that affect the climate as little as possible. Solar power could be the solution if there were solar panels with a less energy demanding production than the established silicon based solar modules. Printable organic solar cells will enable a cheap production process, thus they are mainly made out of polymers in solution. However, to be able to decrease the total cost of the solar modules the commonly used indium tin oxide (ITO) for the transparent electrode needs to be replaced by a less expensive material. If the cheap, high conductive and transparent polymer poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) could replace ITO the cost of organic solar modules would significantly decrease. For PEDOT:PSS to be able to replace ITO there are requirements that have to be met. The transparent electrode needs to be apart from transparent, highly conductive, have a low contact resistance to the other materials in the organic solar cell and be printable. In this study it has been shown that the PEDOT:PSS film with Zonyl and Diethylene Glycol (DEG) as an secondary dopant, is capable of laminating to thin films made out of PEDOT:PSS, metal or a polymer fullerene blend. The contact resistances between two PEDOT:PSS films and PEDOT:PSS film and a metal film proved to be low. When laminating to a metal film an interlayer of Silver Nano Wires (AgNW) was needed to achieve a low contact resistance.

This thesis aims at developing a method of chemical aftertreatment for reduction of free formaldehyde release of a tetrakis (hydroxymethyl) phosphonium chloride (THPC) urea precondensate, ammonia cured durable flame retardant finished cotton fabric, by preventing the formation of free formaldehyde. Formaldehyde is toxic and carcinogenic. According to the worldwide standards, acceptable limit of free formaldehyde release, for the fabrics that have skin contact, is only 75 ppm (measured by water extraction method). In this research, a cotton fabric flame retardant finished in an industrial plant in Pakistan is used. Fabric is finished by the application of THPC urea precondensate and ammonia cured, oxidized and washed. After finishing, it is not aftertreated with sodium metabisulfite that is a commonly used aftertreatment method for the reduction of free formaldehyde release. Aftertreatment with sodium metabisulfite has various problems that include large number of hot washings and there is an increase in the formaldehyde release during fabric storage. If the fabric has 75 ppm of free formaldehyde, there is often an increase in free formaldehyde release during fabric storage. There is a very limited research on the aftertreatment methods and few reports of application of these aftertreatments on flame retardant fabrics have been published. In this research, two methods of aftertreatments are developed to reduce the free formaldehyde contents to 75 ppm or less. One is the aftertreatment with a combination of resorcinol 1% and diethylene glycol 4%. The other is the combination of resorcinol 1% and boric acid 6%. For both these aftertreatments, ammonium acetate 0.5% is used as a catalyst. Fabric is padded with the solution and then dried at 130̊ C for 8 minutes. After drying, fabric is rinsed with water at 40̊ C. The aftertreatment methods developed in this research have shown a long term effect in keeping the formaldehyde release below 75 ppm during fabric storage that is not available with other conventional aftertreatment methods. These aftertreatment methods have no adverse effect on the flame retardancy of the THPC ammonia cured finished fabric and the fabric is soft as compared to the original flame retardant finished fabric and to the fabric after treated with existing methods. These new developed methods have industrial application because there is no use of any solvent and there is no use of any special equipment for the aftertreatment.

<p>Additive manufacturing of gun propellants is an emerging and promising field which addresses the limitations of conventional manufacturing techniques. Gun propellants are manufactured using wetted extrusion, which uses volatile solvents and dies of limited and constant geometries. On the other hand, additive techniques are faced with the challenges of maintaining the gun propellant’s energetic content as well as its structural integrity during high pressure combustion. The work presented in this thesis demonstrates the feasibility of producing functioning gun propellant grains using vibration-assisted 3D printing, a novel method which has been shown to extrude extremely viscous materials such as clays and propellant pastes. At first, the technique is compared to screw-driven additive methods which have been used in printing gun propellant pastes with slightly lower energetic content. In chapter two, diethylene glycol dinitrate (DEGDN), a highly energetic plasticizer, was investigated due to its potential to replace nitroglycerin in double base propellants with high nitroglycerin content. A novel isoconversional method was applied to analyze its decomposition kinetics. The ignition and lifetime values of diethylene glycol dinitrate were obtained using the new isoconversional method, in order to assess the safety of using the plasticizer in a modified double base propellant. In chapter three, a modified double base propellant (M8D) containing DEGDN was additively manufactured using VAP. The printed strands had little to no porosity, and their density was nearly equal to the theoretical maximum density of the mixture. The strands were burned at high pressures in a Crawford bomb and the burning was visualized using high speed cameras. The burning rate equation as a function of the M8D propellant as a function of pressure was obtained. Overall, this work shows that VAP is capable of printing highly energetic gun propellants with low solvent content, low porosity, with high printing speeds, and which have consistent burning characteristics at high pressures. </p>

De nouveaux glycopolymères greffés aux paramètres macromoléculaires contrôlés [dextrane-g-poly(acrylate de diéthylène glycol cholestéryle), Dex-g-PADEGChol] ont été préparés en quatre étapes via la stratégie de synthèse « grafting from». L'originalité de ces glycopolymères réside dans la combinaison, et pour la première fois, d'une dorsale polysaccharide hydrophile biocompatible/ biodégradable et de greffons polymères hydrophobes à caractère mésogène. L'ATRP a été utilisée pour contrôler la croissance des greffons PADEGChol en milieu homogène à partir d'un macroamorceur dérivé de dextrane (DexAcBr). Les conditions de polymérisation avaient été préalablement ajustées en étudiant l'homopolymérisation du monomère ADEGChol en présence d'un amorceur modèle et de plusieurs systèmes catalytiques CuIBr/(PMDETA ou OPMI) dans différents solvants (THF ou toluène). Le caractère amphiphile de ces glycopolymères a été évalué et leurs propriétés mésomorphes ont été étudiées par calorimétrie différentielle à balayage, microscopie optique à lumière polarisante et par diffraction des rayons X. Des études préliminaires par microscope électronique à transmission et diffusion dynamique de la lumière polarisée ont démontré que ces glycopolymères adoptent une morphologie vésiculaire appelée « polymersome » en phase aqueuse, lorsque le DMSO est utilisé comme co-solvant. Ces nano-objets pourront être testés ultérieurement pour la formulation d'un nouveau type de vecteurs de principes actifs / New graft glycopolymers with well-defined parameters [dextran-g-poly(diethylene glycol cholesteryl ether acrylate) (Dex-g-PADEGChol)] have been prepared in four steps using the "grafting from" strategy. Challenge of this work arises from the combination for the first time of a hydrophilic, biocompatible/biodegradable polysaccharide backbone with mesogen hydrophobic polymeric grafts. Controlled growth of the grafts (PADEGChol) was obtained using ATRP initiated in homogeneous medium from a dextran derivative (DexAcBr). In order to find the best polymerization conditions, homopolymerization of ADEGChol monomer was investigated using an initiator model and various catalytic systems CuIBr/(PMDETA or OPMI) in two solvents (Toluene and THF). The amphiphilic properties of such glycopolymers were evaluated and their mesomorphic properties have been studied by thermal polarizing optical microscopy, differential scanning calorimetry and X-ray scattering. Using transmission electron microscopy and dynamic light scattering, vesicular morphology called "polymersome" was observed in aqueous medium when DMSO was used as co-solvent. These polymersomes could be tested as new drug delivery systems