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Characterization of photocurable networks in real-time and post-exposure /Zumbrum, Michael Allen, January 1990 (has links)
Thesis (Ph. D.)--Virginia Polytechnic Institute and State University, 1990. / Vita. Abstract. Includes bibliographical references (leaves 201-210). Also available via the Internet
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High performance polymeric networks and thermoplastic blends : microwave versus thermal processing /Hedrick, Jeffrey C., January 1990 (has links)
Thesis (Ph. D.)--Virginia Polytechnic Institute and State University, 1991. / Vita. Abstract. No film copy made for this title. Includes bibliographical references (leaves 243-254). Also available via the Internet.
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A rheological and structural study of polymer networksFranse, Marcel Willem Cornelis Petrus, January 1900 (has links)
Thesis (doctoral)--Technische Universiteit Delft, 2002. / "Ter verkrijging van de graad van doctor aan de Technische Universiteit Delft, op gezag van de Ractor Magnificus Prof. dr. ir. J.T. Fokkema in het openbaar te verdedigen op dinsdag 29 oktober 2002 om 13:30 uur door." Includes bibliographical references.
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A rheological and structural study of polymer networksFranse, Marcel Willem Cornelis Petrus, January 1900 (has links)
Thesis (doctoral)--Technische Universiteit Delft, 2002. / "Ter verkrijging van de graad van doctor aan de Technische Universiteit Delft, op gezag van de Ractor Magnificus Prof. dr. ir. J.T. Fokkema in het openbaar te verdedigen op dinsdag 29 oktober 2002 om 13:30 uur door." Includes bibliographical references.
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The rational design of recognitive polymeric networks for sensing applicationsNoss, Kimberly RyAnne. Byrne, Mark E., January 2009 (has links)
Thesis (Ph. D.)--Auburn University, 2009. / Abstract. Vita. Includes bibliographical references.
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The elasticity and growth of rigid networksJones, Janette Louise January 1990 (has links)
No description available.
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Diffusion inside polymer networks. / CUHK electronic theses & dissertations collectionJanuary 2000 (has links)
by Jiang Suhong. / "2000." / Thesis (Ph.D.)--Chinese University of Hong Kong, 2000. / Includes bibliographical references. / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web. / Abstracts in English and Chinese.
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Morphological studies of sbs based interpenetrating polymer networksMarkotsis, Martin G., School of Chemical Engineering & Industrial Chemistry, UNSW January 2005 (has links)
Interpenetrating polymer networks (IPNs) of polystyrene-polybutadiene-polystyrene (SBS) block copolymers and polystyrene (PS) were prepared using sequential network formation with the polybutadiene (PB) of the SBS crosslinked thermally and the styrene network formed thermally or by ??-radiation. The use of ??-radiation to cure the added PS network at room temperature successfully avoided thermal degradation of the butadiene segments within the SBS which had been observed in earlier studies. Both linear SBS and radial SB4 IPNs were studied to compare the influence of linear or branched block copolymers on the IPN morphology. The molecular morphology was examined using a suite of techniques including thermal analysis (DSC and DMA), transmission electron microscopy (TEM), atomic force microscopy (AFM) and smallangle X-ray and neutron scattering (SAXS and SANS). The primary SBS/SB4 network morphology was found to dominate the IPN morphology with the secondary styrene network limited to selectively swelling the PS domains. The linear SBS IPNs displayed a more ordered morphology than the radial SB4 IPNs, and this morphology was investigated in pseudo three-dimensions by sectioning samples in two perpendicular directions. The morphology was found to be consistent with thermally formed systems prepared in previous studies, and contained styrenic domains of 20-50 nm within a continuous butadiene matrix. The weight of evidence suggested that the lamella structure dominated the linear SBS IPNs and a cylindrical structure for the radial SB4 IPNs. Maximum values of tensile strength and elongation at break (20 MPa and 140% respectively) were observed in samples with a styrene cure ??-radiation dose of 200 kGy. The SANS analysis of these polymer systems was expanded to investigate the thermal formation of the added PS network in real time. Time-resolved SANS allowed the development of nanostructures in the bulk samples to be measured, and compared to previous time-independent TEM studies on thin sections. The formation of the styrene network was most noticeably observed in a linear SBS IPN system, in which an increase in long-range order was observed and attributed to movement of styrene monomer into the styrenic domains and sharpening of the phase boundaries between the PS and the PB regions.
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Preparation of interpenetrating polymer networks for improved cellulose ester plasticsHo, Shih-Wei 14 December 1998 (has links)
Graduation date: 1999
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Effects of nano structure on the deformation behavior of polymeric networksHu, Qiang 05 1900 (has links)
No description available.
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