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Poly(imide-siloxane) segmented copolymer structural adhesives prepared by bulk and solution thermal imidizationThe improved properties that have been demonstrated through thermal solution imidization in the case of polyimides and poly(imide-siloxane) segmented copolymers suggests significant potential for application of these new materials. Specifically, the enhancement in solubility, moisture reduction, and processability observed through this solution technique is quite dramatic. Previous work has shown that the presence of low amounts of siloxane does not detract significantly from the lap shear strength of these materials to titanium in the case of bulk thermal imidization synthesis. In addition, the siloxane incorporation results in the added advantage of resistance to hot, wet environments. This added durability is presumably due to the hydrophobic siloxane segments preventing the uptake of water at the critical interphase between the adhesive and the adherend. This paper discusses the extension of this work to the solution imidization synthesis technique recently developed in our laboratory. Results dealing with the absolute bond strengths as well as durability and failure surface analysis will be presented.
Document ID
19880055172
Acquisition Source
Legacy CDMS
Document Type
Conference Paper
Authors
Bott, R. H.
(Virginia Polytechnic Inst. and State Univ. Blacksburg, VA, United States)
Summers, J. D.
(Virginia Polytechnic Inst. and State Univ. Blacksburg, VA, United States)
Arnold, C. A.
(Virginia Polytechnic Inst. and State Univ. Blacksburg, VA, United States)
Blankenship, C. P., Jr.
(Virginia Polytechnic Inst. and State Univ. Blacksburg, VA, United States)
Taylor, L. T.
(Virginia Polytechnic Institute and State University Blacksburg, United States)
Date Acquired
August 13, 2013
Publication Date
January 1, 1988
Subject Category
Nonmetallic Materials
Meeting Information
Meeting: Materials - Pathway to the future
Location: Anaheim, CA
Country: United States
Start Date: March 7, 1988
End Date: March 10, 1988
Sponsors: SAMPE
Accession Number
88A42399
Distribution Limits
Public
Copyright
Other

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