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Toughening mechanisms in elastomer-modified epoxies

dc.contributor.authorPearson, Raymond A.en_US
dc.contributor.authorYee, Albert F.en_US
dc.date.accessioned2006-09-11T15:08:37Z
dc.date.available2006-09-11T15:08:37Z
dc.date.issued1986-07en_US
dc.identifier.citationYee, A. F.; Pearson, R. A.; (1986). "Toughening mechanisms in elastomer-modified epoxies." Journal of Materials Science 21(7): 2462-2474. <http://hdl.handle.net/2027.42/44685>en_US
dc.identifier.issn0022-2461en_US
dc.identifier.issn1573-4803en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44685
dc.description.abstractSome brittle epoxies can be toughened significantly by the addition of an elastomeric phase. A great deal of controversy still exists on the nature of the toughening mechanisms. In this work tensile dilatometry at constant displacement rates was used to determine whether voiding, crazing or shear banding are the deformation mechanisms. Diglycidyl ether-bisphenol A epoxies toughened by various levels of several types of carboxyl-terminated butadiene nitrile liquid rubber were studied. The results indicate that at low strain rates the rubber particles simply enhance shear deformation. At sufficiently high strain rates the rubber particles cavitate and subsequently promote further shear deformation. No indication of crazing as an important toughening mechanism is found. No significant effect of rubber particle size or type can be ascertained.en_US
dc.format.extent1137986 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Chapman and Hall Ltd. ; Springer Science+Business Mediaen_US
dc.subject.otherIndustrial Chemistry/Chemical Engineeringen_US
dc.subject.otherChemistryen_US
dc.subject.otherPolymer Sciencesen_US
dc.subject.otherCharacterization and Evaluation Materialsen_US
dc.subject.otherMechanicsen_US
dc.titleToughening mechanisms in elastomer-modified epoxiesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelEngineering (General)en_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumPolymer Physics and Engineering Branch, Corporate Research and Development, General Electric Co., 12301, Schenectady, New York, USA; Department of Materials Science and Engineering, University of Michigan, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherPolymer Physics and Engineering Branch, Corporate Research and Development, General Electric Co., 12301, Schenectady, New York, USA; General Electric Plastics Europe, PO Box 117, 4600, AC Bergen op Zoom, The Netherlandsen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44685/1/10853_2005_Article_BF01114293.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01114293en_US
dc.identifier.sourceJournal of Materials Scienceen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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