The diploma thesis in the first part deals with a theoretical description of coating technologies, textile materials used in coatings, types of coated polymers and properties of coatings - especially adhesion. The experimental part of the work is devoted to the preparation of textile coatings from polyester fabric and coating based on addition silicone. Using the developed method of sample preparation for T-peel testing of the adhesive strength, the improvement of the adhesion of the coating by chemical adhesion with the support of adhesive agents was studied. The second method studied the change in compactness and adhesion of the coating to the fabric after shaking as a function of breathability. The influence of side reactions of reagents on silicone cohesion was studied by preparing dogbones for testing tensile-deformation properties. The research also included the characterization of silicone samples using ATR-FTIR, monitoring the weight gain and thickness of the fabric after coating, the feel and color stability of the applied fabric and observing the coating under an optical microscope.

For grafting polypyrrole on oxidized surfaces, 3-substituted pyrrole alkyl phosphonic acids, 11-(pyrrol-3-yl undecyl) trimethoxysilanes and 1-substituted pyrrole alkyl organosilanes with different chain length were designed and successfully synthesized as adhesion promoters. These new derivatives were studied for their adsorption behavior on oxide substrates and chemical or electrochemical deposition of polypyrrole over modified oxide surface or electrodes. Several analytical techniques such as contact angle measurement, surface plasmon resonance spectroscopy (SPR), UV-VIS Spectroscopy, grazing incident FTIR, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to characterize the adsorbed layers on different substrates. Contact angle measurement and ellipsometry data showed that high concentrations in apolar hydrocarbon solvent and long reaction times are sufficient to form tightly packed monolayer of 1-substituted pyrrole alkyl monochlorosilanes (PMCS) on substrates. Adsorption kinetics were studied by SPR and showed that the adsorption took place within a few seconds, then continuously increased and reached a plateau. The orientation of these synthesized monomers is investigated to be well-suited for use as adhesion promoter. CV-measurements showed that 3-substrated pyrrole derivatives had lower oxidation potential, whereas 1-substituted pyrrole derivatives had higher oxidation potential compared with pyrrole. Surface deposition of polypyrrole on the adhesion promoter modified (silane-modified and phosphonic acid-modified) substrates by chemical and electrochemical polymerization were investigated. PPy films formed on the modified surfaces by surface chemical polymerization showed a better adhesion compared to those on the unmodified surfaces. The morphology of PPy films was influenced by the alkyl chain length of the adhesion promoter and the deposition condition, such as choice of oxidant and solvent. The thickness of the resulting PPy films were controlled by the polymerization conditions, such as choice of solvent, deposition time, pyrrole to oxidant ratio and monomer concentration. The thickness of the deposited PPy film was estimated in the range of 10-400 nm by AFM and ellipsometry. The electrical properties were studied by current-voltage (j-V) measurement. Temperature dependence of j-V characteristics of Si/SiO2/PPy/PMCS-16/Al films revealed that the current increases with temperature, the film shows a typical semiconductor behavior. The use of these adhesion promoters modified electrode for electrochemical polymerization resulted in adhesive polypyrrole films.Also the 3-substituted pyrrole phosphonic acids were found to be homo-and co-polymerizable (with pyrrole) under chemical methods. TGA showed that homopolymers are less stable than polypyrrole due to the 3-substitution. he homopolymer of 3-substituted phosphonic acid derivatives of pyrrole is soluble. Films coated from the MeOH solution of homopolymer could be successfully used as humidity sensors. It is observed that the resistivity of the 3-substituted homopolypyrrole sensors increases and capacitance decreases during exposure to humid air. The polypyrrole films obtained by surface chemical polymerization was also used as humidity sensors.

For grafting polypyrrole on oxidized surfaces, 3-substituted pyrrole alkyl phosphonic acids, 11-(pyrrol-3-yl undecyl) trimethoxysilanes and 1-substituted pyrrole alkyl organosilanes with different chain length were designed and successfully synthesized as adhesion promoters. These new derivatives were studied for their adsorption behavior on oxide substrates and chemical or electrochemical deposition of polypyrrole over modified oxide surface or electrodes. Several analytical techniques such as contact angle measurement, surface plasmon resonance spectroscopy (SPR), UV-VIS Spectroscopy, grazing incident FTIR, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to characterize the adsorbed layers on different substrates. Contact angle measurement and ellipsometry data showed that high concentrations in apolar hydrocarbon solvent and long reaction times are sufficient to form tightly packed monolayer of 1-substituted pyrrole alkyl monochlorosilanes (PMCS) on substrates. Adsorption kinetics were studied by SPR and showed that the adsorption took place within a few seconds, then continuously increased and reached a plateau. The orientation of these synthesized monomers is investigated to be well-suited for use as adhesion promoter. CV-measurements showed that 3-substrated pyrrole derivatives had lower oxidation potential, whereas 1-substituted pyrrole derivatives had higher oxidation potential compared with pyrrole. Surface deposition of polypyrrole on the adhesion promoter modified (silane-modified and phosphonic acid-modified) substrates by chemical and electrochemical polymerization were investigated. PPy films formed on the modified surfaces by surface chemical polymerization showed a better adhesion compared to those on the unmodified surfaces. The morphology of PPy films was influenced by the alkyl chain length of the adhesion promoter and the deposition condition, such as choice of oxidant and solvent. The thickness of the resulting PPy films were controlled by the polymerization conditions, such as choice of solvent, deposition time, pyrrole to oxidant ratio and monomer concentration. The thickness of the deposited PPy film was estimated in the range of 10-400 nm by AFM and ellipsometry. The electrical properties were studied by current-voltage (j-V) measurement. Temperature dependence of j-V characteristics of Si/SiO2/PPy/PMCS-16/Al films revealed that the current increases with temperature, the film shows a typical semiconductor behavior. The use of these adhesion promoters modified electrode for electrochemical polymerization resulted in adhesive polypyrrole films.Also the 3-substituted pyrrole phosphonic acids were found to be homo-and co-polymerizable (with pyrrole) under chemical methods. TGA showed that homopolymers are less stable than polypyrrole due to the 3-substitution. he homopolymer of 3-substituted phosphonic acid derivatives of pyrrole is soluble. Films coated from the MeOH solution of homopolymer could be successfully used as humidity sensors. It is observed that the resistivity of the 3-substituted homopolypyrrole sensors increases and capacitance decreases during exposure to humid air. The polypyrrole films obtained by surface chemical polymerization was also used as humidity sensors.

The adhesion of coatings is of high importance in the coating industry and a more thorough understanding of adhesion behavior is required. In this thesis work, seven parameters affecting adhesion of silane-modified poly(urethane urea) (PUSi) coatings on pretreated steel and aluminum substrates were studied. These parameters include substrate type, dry film thickness (20-30 and 60-70 μm), solid content (40, 60, and 70 wt%), resin ratio between two different types of PUSi (PUSi-A: PUSi-B = 70:30, 50:50, and 30:70 wt ratio), crosslinking density, additive, and curing condition. The different pretreatments of substrates include solvent wiping, sandblasting, phosphating, and galvanizing. A commercial paint product (‘yellow topcoat’) was used as a reference for the study of substrates and additives. Several formulations of clearcoat, prepared from the same PUSi resins as the commercial paint product, were mainly used in every experiment. The obtained coatings were tested for their adhesion properties using cross hatch adhesion test, bending test, and humidity resistance test. The film hardness and thermo-mechanical properties were evaluated with König pendulum hardness test and Dynamic Mechanical Analysis (DMA), respectively. Surface energies of all substrates were analyzed with Contact Angle Measurement (CAM). The PUSi-A and PUSi-B resins used in the coating formulations were characterized with Differential Scanning Calorimetry (DSC), Size-Exclusion Chromatography (SEC), and Fourier Transform Infrared Spectroscopy (FT-IR). The results showed a correlation between poor adhesion properties and the relatively low surface energies of some substrates, namely cold-rolled steel (CRS), industrial ACE aluminum, and standard Q aluminum. The use of silane-functional crosslinking agent and silane adhesion promoters in the coatings has greatly enhanced adhesion. The increase in film hardness via increased crosslinking density also did not hinder the adhesion due to the presence of silane groups in the crosslinker. Additionally, increased time and temperature during curing showed positive effects. However, the variation of resin ratio, solid content, and film thickness did not offer significant adhesion improvement in this study. / Adhesionsegenskaperna hos ytbeläggningar är av stor betydelse i färg- och lackindustrin och en djupare förståelse av vidhäftning är av stor betydelse. I detta uppsatsarbete studerades sju parametrar som påverkar vidhäftning av silanmodifierad poly(uretan-urea) (PUSi)-beläggningar på stål- och aluminiumsubstrat. Dessa parametrar inkluderar substrattyp, torr filmtjocklek (20-30 och 60-70 μm), torrhalt (40, 60 och 70 viktprocent), mängdförhållandet mellan två olika typer av PUSi (PUSi-A: PUSi-B = 70:30, 50:50 och 30:70 viktprocent), tvärbindningsdensitet, tillsatsmedel och härdningsbetingelser. Förbehandlingen av substraten inkluderar lösningsmedelsavtorkning, sandblästring, fosfatering och galvanisering. En kommersiell ytbehandlingsprodukt innehållandes gula pigment (gul topplack) användes som referens. Flera formuleringar av klarlack, framställda av samma PUSi-hartser som den kommersiella produkten, användes i det experimentella arbetet. Beläggningarna testades med avseende på deras vidhäftningsegenskaper med ’cross-hatch’-test, böjningstest och fuktbeständighetstest. Filmhårdhet och termomekaniska egenskaper utvärderades med König pendelhårdhetstest respektive Dynamisk Mekanisk Analys (DMA). Ytenergier för alla substrat analyserades med kontaktvinkelmätning (CAM). PUSi-A- och PUSi-B-hartserna som användes i ytbeläggningarna karaktäriserades med Differential Scanning Calorimetry (DSC), Size-Exclusion Chromatography (SEC) och Fourier Transform Infrared Spectroscopy (FT-IR). Resultaten visade en korrelation mellan dålig vidhäftning och låga ytenergier för vissa underlag, främst kallvalsat stål (CRS), industriellt ACE-aluminium och standard Q-aluminium. Användningen av silan-funktionell tvärbindare och en silan-baserad primer förbättrade vidhäftningen avsevärt. Ökningen i filmhårdhet genom högre tvärbindningsdensitet resulterade inte i sämre vidhäftning eftersom tvärbindaren innehåller silan-grupper vilket bidrog till att upprätthålla vidhäftningen. Längre tid och högre temperatur vid härdning gav generellt bättre vidhäftning, liksom tillsats av urea. Att variera mängden bindemedel, torrhalt eller filmtjocklek gav inte någon signifikant påverkan på vidhäftning i denna studie.