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A new dual-stage multicomponent thermosetting polymer system /Brouns, Richard Allan, January 1993 (has links)
Thesis (Ph. D.)--University of Washington, 1993. / Vita. Includes bibliographical references (leaves [108]-113).
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Accelerated degradation of composite adhesive bondsPothakamuri, Prasanthi, January 2006 (has links) (PDF)
Thesis (M.S.)--Washington State University, December 2006. / Includes bibliographical references (p. 80-84).
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Synthesis and structure property studies in acrylic pressure sensitive adhesives /Tobing, Singa D., January 1999 (has links)
Thesis (Ph. D.)--Lehigh University, 2000. / Includes bibliographical references and vita.
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Photodegradation of adhesives used in wood composite materialsMiesner, Martin 11 1900 (has links)
The weathering of wood composites is caused by a complex combination of chemical and mechanical effects. Wood composites such as glulam beams are increasingly being used outdoors where their service life depends to some extent on the durability of the adhesive used in the composite. Increases in the durability of adhesives used in such composite materials would prolong their service life and enable them to compete more effectively with other structural materials such as concrete and steel. This study attempted to improve our understanding of the photodegradation of adhesives and the relationship between wood and adhesive photodegradation. The effectiveness of a UV light absorber and hindered amine light stabilizer (UVA and HALS) at protecting adhesives from photodegradation was also investigated. First, the effect of adhesive type (melamine formaldehyde, epoxide, and emulsion polymer isocyanate), stabilizer and adhesive stabilizer interaction on tensile strength, weight loss and discoloration of adhesive dog-bone samples exposed in two different weatherometer devices (QUV and Xenon-arc) was examined. Structural and chemical changes of the adhesive specimens were examined using Fourier Transform Infrared (FTIR) spectroscopy and Scanning Electron Microscopy (SEM). Secondly, the effects of adhesive type (melamine formaldehyde, epoxide), stabilizer and adhesive stabilizer interaction on surface roughness and discoloration of wood-adhesive-dowel samples exposed to solar radiation was examined. Profileometry and SEM was used to examine the surface of dowels in the region where they were exposed to both wood and sunlight. An epoxide adhesive (butyl glycidyl ether of bisphenol-A with polyamide) used in the aircraft industry showed outstanding resistance to weathering. The other adhesives were not as resistant to weathering, but the addition of a UVA/HALS photostabilizer to the adhesives generally increased their photostability (particularly color changes of the epoxy adhesives and weight loss of the MF adhesive). Greater degradation of adhesive samples occurred when they were exposed in a QUV weatherometer than in a Xenon-arc weatherometer. The synergistic effect of moisture and UV radiation on the degradation of adhesives may account for this observation. Adhesive dowels embedded in wood did not show greater degradation (erosion) in the region where they were exposed to both wood and sunlight. Therefore the hypotheses that wood photosensitizes adhesives could not be supported by experimental findings. Further refinement of the experimental methodology developed in this thesis would be desirable to retest this hypothesis. All of the four adhesives that were tested possessed some interesting characteristics that might make them suitable for use in glulam exposed outdoors, but out of the four the two epoxy adhesives appeared to have the greatest potential. / Forestry, Faculty of / Graduate
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The rheology and strength of hot melt adhesivesDoody, Paul David January 1997 (has links)
Various properties of the components and adhesives were modelled. The compatibility of the components were successfully incorporated into an extended Fox equation to predict the glass transition temperature. The peel strength of the adhesive was modelled in terms of the rheological properties of elastic moduli and loss tangent values at different temperatures. A second model based upon the value of the loss tangent at room temperature was also broadly successful but deviations from predicted behaviour were observed which were attributable to failure of the adhesive joints by a mode not included in the model. The modulus of the adhesive was modelled on the basis of an extended mixture rule in which the extent of compatibility was identified by a parameter n. The value of n varied as a function of adhesive composition and temperature, indicating that the behaviour of the adhesives changed subtly as the compatibility of the phases changed. The value of the parameter could not be directly related to the morphology of the adhesive phases. Fourteen commercially available poly(ethylene-co-vinyl acetate) (EVA) copolymer samples were selected in which there was a systematic change in the melt index, amount of vinyl acetate, and degree of crystallinity. Various hot melt adhesives were made using these copolymers and a standard amount of wax and resin. The materials were examined using differential scanning calorimetry (DSC), oscillatory rheometry (both controlled strain and controlled stress), and transient (creep) rheometry. The adhesives were also investigated using a variety of industrial tests which included peel adhesion and tensile testing at four different rates, open and setting time, shear and peel stress resistance at elevated temperatures, and viscosity determination over a wide range of temperatures. Detailed thermal analysis and characterisation have provided a range of accurate and systematic data on all of the materials and in particular showed that the components of the adhesive did not merely act as a mechanical mixture but had a distinct compatibility. The controlled stress technique was found to more discriminatory than the controlled strain, due to the more precisely controlled heating and cooling of the sample during loading and evaluation. Other key differences between the techniques are attributable to the different thermal histories imposed upon the semi-crystalline adhesive components. Detailed analysis of the complex rheological curves showed several key factors. One of the most important was the modulus crossover temperature Tx which was shown to correlate well with the softening point of the adhesive, its open time, and the heat resistance under shear as determined by the shear adhesion failure temperature (SAFT). It was possible to construct a linear relationship between Tx and SAFT which allowed prediction of this key adhesive parameter. There was no significant relationship established between the softening point of an adhesive and its heat resistance, open time, or critical thermal characteristics, and the use of the softening point as a useful indicator of adhesive performance is contested. The open time was shown to be clearly influenced by the properties of the copolymer. The relationship between open time and melt index is complex and two competing mechanisms are thought responsible. These are the inability to fully wet the substrate for high molecular weights and resistance to complete substrate penetration by capillary effects for adhesives formulated with low molecular weight polymers. Both of these effects cause a reduction in open time. The cloud points of the adhesives were independent of the molecular weight but strongly affected by composition. Degree of crystallinity was also an influence at higher molecular weights. Cloud point correlated slightly with the onset of crystallisation as determined by DSC however differences are extremely small and the method was not deemed robust enough for widespread industrial application. Various properties of the components and adhesives were modelled. The compatibility of the components were successfully incorporated into an extended Fox equation to predict the glass transition temperature. The peel strength of the adhesive was modelled in terms of the rheological properties of elastic moduli and loss tangent values at different temperatures. A second model based upon the value of the loss tangent at room temperature was also broadly successful but deviations from predicted behaviour were observed which were attributable to failure of the adhesive joints by a mode not included in the model. The modulus of the adhesive was modelled on the basis of an extended mixture rule in which the extent of compatibility was identified by a parameter n. The value of n varied as a function of adhesive composition and temperature, indicating that the behaviour of the adhesives changed subtly as the compatibility of the phases changed. The value of the parameter could not be directly related to the morphology of the adhesive phases.
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Tensile bond and rebond strength of four orthodontic adhesives a thesis submitted in partial fulfillment ... orthodontics ... /Wright, William L. January 1984 (has links)
Thesis (M.S.)--University of Michigan, 1984.
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Tensile bond and rebond strength of four orthodontic adhesives a thesis submitted in partial fulfillment ... orthodontics ... /Wright, William L. January 1984 (has links)
Thesis (M.S.)--University of Michigan, 1984.
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Effect of a protective dressing and adhesives on retention of maxillofacial prosthesesKiat-amnuay, Sudarat, January 1999 (has links)
Thesis (M.S.)--University of Louisville, 1999. / School of Dentistry, Program in Oral Biology. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
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Effect of a protective dressing and adhesives on retention of maxillofacial prosthesesKiat-amnuay, Sudarat, January 1999 (has links)
Thesis (M.S.)--University of Louisville, 1999. / School of Dentistry, Program in Oral Biology. Includes bibliographical references.
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Adhesive bonding of thermoplastic fibre-compositesKodokian, George-Kevork January 1989 (has links)
No description available.
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