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As clean energy demand is on the rise and the wind energy sector in growth, locations with the highest wind potential are becoming of higher interest for wind farm projects, but they are located in colder regions. In cold climates, ice accumulation on wind turbine blades is a serious issue, both in terms of safety and performance. To prevent this, anti-icing technologies, such as Vestas Wind Systems A/S’s, electro-thermal elements are added to wind turbine blades’ construction. This thesis project consists of developing a method to investigate the heat transfer inside and out of wind turbine blades to assess the performance of the anti-icing system and most importantly, verify if it could lead to thermal damage of the blade’s adhesive. In an integrated MATLAB code, the heating requirement is calculated and the 2D conduction modelled based on the wind conditions. The output is a temperature map of the internal structure along with the points with the highest temperature for all adhesive locations, which shows that the selected heating power provided by the heating elements compromises the integrity of the adhesive and doesn’t perform to allow the surface temperature to reach the necessary threshold the prevent icing.

Single wavelength ellipsometry measurements at Brewster's angle provide a powerful technique for characterizing ultrathin polymeric films. By conducting the experiments in different ambient media, multiple incident media (MIM) ellipsometry, simultaneous determinations of a film's thickness and refractive index are possible. Poly(tert-butyl acrylate) (PtBA) films serve as a model system for the simultaneous determination of thickness and refractive index (1.45 at 632 nm). Thickness measurements on films of variable thickness agree with X-ray reflectivity results. The method is also applicable to spincoated films where refractive indices of PtBA, polystyrene and poly(methyl methacrylate) are found to agree with literature values within experimental error. Likewise, MIM ellipsometry is utilized to simultaneously obtain the refractive indices and thicknesses of thin films of trimethylsilylcellulose (TMSC), regenerated cellulose, and cellulose nanocrystals where Langmuir-Blodgett (LB) films of TMSC serve as a model system. Ellipsometry measurements not only provide thickness and optical constants of thin films, but can also detect thermally induced structural changes like surface glass transition temperatures (Tg) and layer deformation in LB-films. Understanding the thermal properties of the polymer thin films is crucial for designing nanoscale coatings, where thermal properties are expected to differ from their corresponding bulk properties because of greater fractional free volume in thin films and residual stresses that remain from film preparation. Polyhedral oligomeric silsesquioxane (POSS) derivatives may be useful as a nanofiller in nanocomposite formulations to enhance thermal properties. As a model system, thin films of trisilanolphenyl-POSS (TPP) and two different molar mass PtBA were prepared as blends by Y-type Langmuir-Blodgett film deposition. For comparison, bulk blends were prepared by solution casting and the samples were characterized via differential scanning calorimetry (DSC). Our observations show that surface Tg is depressed relative to bulk Tg and that magnitude of depression is molar mass dependent for pure PtBA films. By adding TPP as a nanofiller both bulk and surface Tg increase. Whereas, bulk Tg shows comparable increases for both molar masses, the increase in surface Tg for higher molar mass PtBA is greater than for lower molar mass PtBA. These studies show that POSS can serve as a model nanofiller for controlling Tg in nanoscale coatings. / Ph. D.

This work addresses the morphology of the wood/ Phenol-Formaldehyde (PF) adhesive interphase using yellow-poplar. In this case, morphology refers to the scale or dimension of adhesive penetration into wood. The objective is to develop methods for revealing ever smaller levels of wood/resin morphology. Dynamic techniques that are commonly utilized in polymer blend studies are investigated as potential methods for probing the wood/ adhesive interphase morphology. These are Dynamic Mechanical Analysis (DMA) and solid state NMR using CP/MAS. PF resin molecular weight is manipulated to promote or inhibit resin penetration in wood, using a very low or a very high molecular weight PF resin. With DMA, the influence of PF resin on wood softening is investigated. It is first demonstrated that the cooperativity analysis according to the Ngai coupling model of relaxation successfully applies to the in-situ lignin glass transition of yellow-poplar and spruce woods. No significant difference in intermolecular coupling is detected between the two woods. It is then demonstrated that combining simple DMA measurements with the cooperativity analysis yields ample sensitivity to the interphase morphology. From simple DMA temperature scans, a low molecular weight PF (PF-Low) does not influence lignin glass transition temperature. However, the Ngai coupling model of relaxation indicates that intermolecular coupling is enhanced with the low molecular weight PF. This behavior is ascribed to the low molecular weight PF penetrating lignin on a nanometer scale and polymerizing in-situ. On the other hand, a high molecular weight resin with a broad distribution of olecular weights (PF-High) lowers lignin glass transition temperature dramatically. This plasticizing effect is ascribed to a small fraction of the PF resin being low enough in molecular weight to penetrate lignin on a nanoscale, but being too dispersed for forming a crosslinked network. With CP/MAS NMR, intermolecular cross-polarization experiments are found unsuitable to probe the angstrom scale morphology of the wood adhesive interphase. However, observing the influence of the PF resins on the spin lattice relaxation time in the rotating frame, HT1r, and the cross-polarization time (TCH) is useful for probing the interphase morphology. None of the resins significantly affects the cross-polarization time, suggesting that angstrom scale penetration does not occur with a low nor a high molecular weight PF resin. However, the low molecular weight PF substantially modifies wood polymer HT1r, indicating that the nanometer scale environment of wood polymers is altered. On the other hand, the high molecular weight PF resin has no effect on wood HT1r. On average, the high molecular weight PF does not penetrate wood on a nanometer scale. Interestingly, the low molecular weight PF resin disrupts the spin coupling that is typical among wood components. Spin coupling between wood components is insensitive to the high molecular weight PF. Finally, it is noteworthy that the two PF resins have significantly different T1r 's in-situ. The low molecular weight resin T1r lies within the range of wood relaxations, suggesting some degree of spin coupling. On the other hand, the T1r of the high molecular weight PF appears outside the range of wood relaxations. Spin coupling between the high molecular weight resin and wood components is therefore inefficient. The CP/MAS NMR and DMA studies converge to identify nanometer scale penetration of the low molecular weight PF in wood. On the other hand, the high molecular weight PF resin forms separate domains from wood, although a very small fraction of the PF-High is able to penetrate wood polymers on a nanoscale. / Ph. D.