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Surface science and stability of networks prepared from hydroxy-terminated polydimethylsiloxane and methyltriethoxysilane

dc.contributor.authorWynne, Kenneth J.en_US
dc.contributor.authorHo, T.en_US
dc.contributor.authorJohnston, E. E.en_US
dc.contributor.authorMyers, Sharon A.en_US
dc.date.accessioned2006-04-28T16:51:47Z
dc.date.available2006-04-28T16:51:47Z
dc.date.issued1998-10en_US
dc.identifier.citationWynne, Kenneth J.; Ho, T.; Johnston, E. E.; Myers, Sharon A. (1998)."Surface science and stability of networks prepared from hydroxy-terminated polydimethylsiloxane and methyltriethoxysilane." Applied Organometallic Chemistry 12(10-11): 763-770. <http://hdl.handle.net/2027.42/38313>en_US
dc.identifier.issn0268-2605en_US
dc.identifier.issn1099-0739en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38313
dc.description.abstractPolydimethylsiloxane (PDMS) hybrid networks have been prepared by the reaction of PDMS(OH) 2 , average molecular weight 26 14× 1410 3 , 43.6 14× 1410 3 and 58 14× 1410 3 , and methyltriethoxysilane (MeTEOS, 10–60 wt%) using a dibutyltin dilaurate or dibutyltin diacetate catalyst. By hydrolysis and homo- and co-condensation, MeTEOS forms a siliceous domain (MeSD) and acts as a crosslinker for the PDMS domain. Kinetic studies showed that high MeTEOS and catalyst concentrations and reduction of free surface area favor fast gelation and efficiency in converting MeTEOS to the MeSD. Under the water-sparse conditions utilized, cure was slow and substantial evaporative loss of MeTEOS occurred. © 1998 John Wiley & Sons, Ltd.en_US
dc.format.extent119178 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherChemistryen_US
dc.subject.otherIndustrial Chemistry and Chemical Engineeringen_US
dc.titleSurface science and stability of networks prepared from hydroxy-terminated polydimethylsiloxane and methyltriethoxysilaneen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationotherMaterials Chemistry Branch, Code 6120, Naval Research Laboratory, Washington, DC 20375, USA ; Physical Science S&T Division-331, Office of Naval Research, Arlington, VA 22217-5660, USA ; Materials Chemistry Branch, Code 6120, Naval Research Laboratory, Washington, DC 20375, USAen_US
dc.contributor.affiliationotherMaterials Chemistry Branch, Code 6120, Naval Research Laboratory, Washington, DC 20375, USA ; Department of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061-0212, USAen_US
dc.contributor.affiliationotherMaterials Chemistry Branch, Code 6120, Naval Research Laboratory, Washington, DC 20375, USA ; Department of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061-0212, USAen_US
dc.contributor.affiliationotherNaval Air Warfare Center, Weapons Division, Chemistry and Materials Branch, China Lake, CA 93555, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38313/1/784_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1099-0739(199810/11)12:10/11<763::AID-AOC784>3.0.CO;2-Cen_US
dc.identifier.sourceApplied Organometallic Chemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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