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Rate and temperature effects on the fracture toughness of a rubber-modified epoxy

dc.contributor.authorCardwell, B. J.en_US
dc.contributor.authorYee, Albert F.en_US
dc.date.accessioned2006-04-10T15:50:04Z
dc.date.available2006-04-10T15:50:04Z
dc.date.issued1993-04en_US
dc.identifier.citationCardwell, B. J., Yee, A. F. (1993/04)."Rate and temperature effects on the fracture toughness of a rubber-modified epoxy." Polymer 34(8): 1695-1701. <http://hdl.handle.net/2027.42/30897>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TXW-48CWS4H-12M/2/225ed1b457d9cabdbad500ac9d6821c1en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30897
dc.description.abstractA series of three-point bend fracture toughness tests was performed at various loading rates and temperatures on both rubber-modified and unmodified epoxy specimens. The fracture toughness of the modified samples was determined to be rate- and temperature-dependent. Using time-temperature superposition, an apparent activation energy was determined by shifting the fracture toughness data along the rate axis for each temperature tested. Surprisingly, this apparent activation energy calculated for the rubber-modified epoxy was found to be within 2% of the value of the activation energy determined for the [beta] relaxation peak found from small strain d.m.a. measurements of the unmodified epoxy matrix. This was an unexpected yet interesting correlation. Since shear yielding is the primary mechanism by which this epoxy system is toughened, it can be hypothesized the [beta] relaxation may significantly influence the kinetics of yielding and consequently the fracture tougness of the material. Plastic zone geometry and fracture mechanisms were investigated and were found to support this hypothesis.en_US
dc.format.extent1508356 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleRate and temperature effects on the fracture toughness of a rubber-modified epoxyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelManagementen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelEconomicsen_US
dc.subject.hlbtoplevelBusinessen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30897/1/0000566.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0032-3861(93)90329-9en_US
dc.identifier.sourcePolymeren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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