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Epoxy resins are widely used as coatings, encapsulations, structural composites, castings, and adhesives in a number of electrical applications. Recently, novel uncatalyzed co-anhydride cured epoxy formulations that exhibit a high performance property profile, have been introduced. The objective of this thesis was to perform a comprehensive material characterization of these new resin/hardener combinations, which are potentially used as electrical insulation material in medium and high voltage engineering. The thermal cure behaviour of commercial tetraglycidyl-diamino-diphenylmethane (TGDDM) and a co-anhydride mixture consisting of maleic anhydride (MA) and hexahydrophthalic anhydride (HHPA) was extensively studied. Different analytical real-time methods, such as FT-Raman spectroscopy, differential scanning calorimetry, and chemo-rheological methods were applied to investigate the principal polymerization mechanism and the related curing kinetics. It was demonstrated that kinetic parameters that were based on isothermal measurements provided consistent and reliable results. On the other hand the general limitations of different dynamic methods for kinetic parameter calculations were outlined and discussed. Temperature modulated differential scanning calorimetry provided a powerful technique to confirm a TGDDM/MA and TGDDM/HHPA sub-network structure of the co-anhydride cured epoxy. A generalized time-temperature-transformation-diagram was developed in order to predict the complex material transformations (e.g. gelation and vitrification) occurring during the entire isothermal curing process. In the selected system, the mechanical deformation and fracture behaviour as a function of temperature, strain rate, inorganic filler fraction, particle size, and filler/matrix-adhesion were thoroughly studied by using compression-, tension- and double torsion fracture-tests. The potential of hyperbranched polymers (HBPs) as low viscosity toughening modifiers for highly crosslinked anhydride-cured epoxy networks was experimentally evaluated. The effects of the HBP molecular structure, in particular the specific shell chemistry, on thermo-mechanical properties, final morphology, and blend concentration, were assessed. For the neat investigated epoxy-system the most efficient toughening modifier was obtained for a molecular HBP-design that provided a pseudo-homogeneous blend morphology. Thus, by using suitable HBPs in a concentration of 20% w/w, the fracture toughness, expressed by the critical stress intensity factor (Klc) of 0.58 MPam(to the power of)0.5, was increased by over 50% to 0.88 MPam(to the power of)0.5. The corresponding Young's modulus and glass transition temperature were only affected to a limited extent by the addition of the HBP-additive. The toughest epoxy blend (critical stress intensity factor of about 1.6 MPam(to the power of)0.5) was achieved by the incorporation of 60% w/w inorganic silica particles. The application of hybrid concepts by utilizing synergistic toughening mechanisms (HBP and silica), revealed only moderate benefits within the investigated highly crosslinked materials. As the examined epoxy/anhydride formulations are generally considered for high temperature applications, it was essential to determine their long-term thermooxidative ageing performance. The long-term thermo-oxidative ageing behaviour has been investigated by means of thermo-gravimetric analysis (TGA), dynamic mechanical analysis (DMA) and vibrational infrared spectroscopy (FT-IR) methods with special emphasis on fundamental understanding of the ageing mechanism. Effects of the thermal ageing on the characteristic viscoelastic and flexural behaviour, weight-loss and oxidation susceptibility of the examined epoxy networks were assessed and discussed, thus providing an understanding of the principal material endurance properties. The thermo-mechanical behaviour and the related structural changes with thermal ageing were examined by Cole-Cole plots in combination with a molecular theory previously developed by Perez. It was demonstrated that this new methodology provides a connection between conversion, glass transition temperature, and mechanical relaxation data and allows a fundamental molecular interpretation with respect to physical and chemical ageing phenomena. A variety of thermo-gravimetric experiments were carried out in order to determine and model the specific weight-loss profile as a function of anhydride nature and ageing temperature. The influence of different inorganic fillers on the thermooxidative response was systematically studied. Different models were applied to extract meaningful kinetic parameters in order to describe the thermo-oxidative degradation and to facilitate an extrapolation of weight-loss data outside the experimental time- and temperature-scale. FT-IR micro ATR-spectroscopy was used to identify, localize and quantify the complex oxidation behaviour. A thermo-oxidative degradation mechanism, that involved predominantly radical oxidation processes and C-N as well as C-O chain scissions, was proposed to account for the experimental observations. Specific oxidation-front profiles were constructed to describe the heterogeneous oxidation processes. Finally, the comprehensive material characterization of these novel co-anhydridecured amino-glycidyl resins in terms of curing mechanism and kinetic, deformation and fracture behaviour, and thermo-oxidative ageing performance, allows the assessment of the potential of these materials for demanding applications in electrical and electronic industries.

Doctor of Philosophy(PhD) / Particle formation in RAFT-mediated emulsion polymerization has been studied using reaction calorimetry. By measuring the heat flow during controlled feed ab-initio emulsion polymerization in the presence of amphipathic RAFT agents, particle formation by self-assembly of these species could be observed. Two different monomer systems, i.e. styrene and n-butyl acrylate, and various degrees of hydrophobicity of the initial macro-RAFT agents have been studied and compared. The different macro-RAFT agents were synthesized by first forming a hydrophilic block of poly(acrylic acid) that would later on act as the electrosteric stabilizing group for the particles. Subsequently, different lengths of hydrophobic blocks were grown at the reactive end of the poly(acrylic acid) hydrophilic block via the RAFT-mediated controlled radical polymerization, either comprised of n-butyl acrylate or styrene. Two processes govern particle formation: adsorption of macro-RAFT agents onto growing particles and formation of new particles by initiation of micellar aggregates or by homogeneous nucleation. Competition between these processes could be observed when monomers with a relatively high (n-butyl acrylate) or low (styrene) propagation rate coefficient were used. A model describing particle formation has been developed and the results of model calculations are compared with experimental observations. Preliminary modeling results based on a set of reasonable physico-chemical parameters already showed good agreement with the experimental results. Most parameters used have been verified experimentally. The development of the molecular weight distribution of the macro-RAFT agents has been analyzed by different techniques. Quantification of the particle formation process by analytical techniques was difficult, but qualitative insights into the fundamental steps governing the nucleation process have been obtained. The amount of macro-RAFT agents initially involved in particle formation could be determined from the increase of molecular weight. The particle size distribution has been measured by capillary hydrodynamic fractionation, transmission electron microscopy and dynamic light scattering. From the data obtained from these particle-sizing techniques, the number of particles during the reaction could be monitored, leading to an accurate estimate for the particle formation time. Upon implementation of the experimental data obtained for the surface active macro-RAFT systems, the model demonstrated to be very sensitive towards the “headgroup” area of the macro-RAFT species. Three nucleation cases based on the initial surface activity of the macro-RAFT species in the aqueous phase are proposed to explain the deviations from the assumptions of the nucleation model. Even though the macro-RAFT species have a narrow molecular weight distribution, they are nevertheless made up of a distribution of block lengths of polystyrene upon a distribution of block lengths of poly(acrylic acid). The resulting differences in initial surface activity are the most probable reason for the observed differences between model calculations and experimental results for the nucleation time and particle size distribution of the final latex product. With the procedure described above, latexes have been synthesized without using conventional surfactants and the mechanisms involved in the particle formation for these systems have been elucidated. The results of this work enable production of latex systems with well defined molecular mass distributions and narrow particle size distributions. Furthermore, the technique based on the application of amphipathic RAFT agents is promising for the production of complex polymeric materials in emulsion polymerization on a technical scale.

Thesis (Ph.D.) -- McMaster University, 1998. / Includes bibliographical references (leaves 207-214). Also available via World Wide Web.

Thesis (M.M.S.E.)--University of Delaware, 2008. / Principal faculty advisor: John F. Rabolt, Dept. of Materials Science & Engineering. Includes bibliographical references.

Stuttgart, Univ., Diss., 2000.

Thesis (Ph. D.)--Ohio State University, 2006. / Title from first page of PDF file. Includes bibliographical references (p. 56-62).

Thesis (M.S.) -- Worcester Polytechnic Institute. / Keywords: measurement uncertainty; composite properties. Includes bibliographical references.

Thesis (Ph. D. in Physics)--Vanderbilt University, Dec. 2007. / Title from title screen. Includes bibliographical references.

Orientador: Claudio Airoldi / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica / Made available in DSpace on 2018-08-04T03:16:55Z (GMT). No. of bitstreams: 1 Machado_MargareteOliveira_M.pdf: 2375635 bytes, checksum: f083ccbf844356a5d576d3d1a2311e97 (MD5) Previous issue date: 2004 / Mestrado / Quimica Inorganica / Mestre em Química