No description available.

Thesis (M.S.)--University of Missouri-Columbia, 2003. / Typescript. Includes bibliographical references (leaves 96-100). Also available on the Internet.

Thesis (M.S.)--University of Missouri-Columbia, 2003. / Typescript. Includes bibliographical references (leaves 96-100). Also available on the Internet.

Thesis (M. S.)--Mechanical Engineering, Georgia Institute of Technology, 2009. / Committee Chair: Colton, Jonathan; Committee Member: Schultz, John; Committee Member: Zhou, Min. Part of the SMARTech Electronic Thesis and Dissertation Collection.

Thesis (M. S.)--Materials Science and Engineering, Georgia Institute of Technology, 2009. / Committee Chair: Gall, Ken; Committee Co-Chair: McDowell, David; Committee Member: Guldberg, Robert; Committee Member: Sanderson, Terry; Committee Member: Shofner, Meisha; Committee Member: Tannenbaum, Rina.

Thesis (M.S.M.E)--University of Delaware, 2006. / Principal faculty advisor: Jian-Qiao Sun, Dept. of Mechanical Engineering. Includes bibliographical references.

No description available.

A series of four water-blown flexible polyurethane foams was produced in which the water content was varied from 2 to 5 pph at a constant isocyanate index of 110. A portion of each foam was thermally compression molded into a plaque. The morphology of the foams and plaques was investigated using DMS, DSC, FTIR, TEM, SEM, swelling, WAXS, and SAXS. A high degree of phase separation occurs in these foams and the degree of phase separation is independent of water (hard segment) content. In the foam with the lowest water content the morphology is similar to that of typical segmented urethane elastomers. Small hard segment domains are present with a correlation distance of roughly 7.0 nanometers. When the water content is increased a binodal distribution of hard segments appears. There are the small hard segment domains typical of segmented urethane elastomers as well as large hard segment aggregates greater than 100 nanometers in diameter. The large domains are thought to be aggregates of polyurea that precipitated during the manufacture of the foam. The foam making process successfully incorporated the trifunctional polyols into a network indicating a high degree of polymerization for the hydroxyl-isocyanate reaction. Unreacted isocyanate is present in the foams a month after curing. It is believed to be trapped in the large urea aggregates. WAXS patterns of the foams suggest hard segment ordering that may be of a paracrystalline nature but certainly lacking in true crystallinity. / Master of Science

A set of flexible water-blown slab stock polyurethane foams and their respective compression molded plaques as well as a chemically similar polyurea-urethane elastomer, PUUE, were studied to better understand the relaxation behavior and the molecular orientation upon deformation in these systems. The two main experimental techniques used in this investigation were stress relaxation in tension and deformation-IR dichroism. The stress relaxation in the foams and their respective plaques increased with hard segment content. The stress relaxation in the foams also appeared to depend very little on its anisotropic cell geometry and hence, mainly on the material comprising, the cell-wall struts and windows. Segmental orientation was measured as a function of elongation and relaxation, as well as hysteresis behavior for several of the plaques and the PUUE elastomer. The orientation changes upon deformation in the soft segments of both materials were small. Small changes in orientation with time and upon cyclic straining were also observed for the soft segments. The orientation at the interface of the hard and soft segments was influenced more by the soft segments in comparison to the hard segments in the plaques and in the PUUE elastomer. Significant transverse orientation upon deformation was observed in the hard segments of the plaques and up to elongations of 100 percent for the PUUE elastomer. Based on this transverse orientation behavior, the polyurea aggregates in the plaques were thought to possess a lamellar-like structure with the long axis of the aggregates aligning in the stretch direction. Relaxation and hysteresis behavior were observed upon following the orientation of the hard segments of the PUUE elastomer, but were negligible in that of the hard segments of the plaques. / Master of Science

No description available.