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dc.identifier.urihttp://hdl.handle.net/11401/76232
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeThesis
dcterms.abstractInterpenetrations (or entanglements) between chemically identical polymers are important parameters in fundamental physics and industrial applications. However, little is known about the interaction between free polymer chains and chemically identical, but otherwise highly adsorbed chains on solid surfaces. Here we report an unusual interaction between free chains and chemically identical flattened chains which have many surface-segmental contacts with solids. Based on the mechanical adhesion measurements, we found the 2.5 nm-thick equilibrium polyethylene-oxide (PEO) flattened layer show no adhesion with the PEO melts even at T >Tm. Liquid contact angle measurements further revealed that the flattened layer has the same macroscopic surface tension compared to thin films. Hence, the unusual interaction between free chains and highly adsorbed flattened chains is not due to a difference in the surface tension, but is associated with the unique chain conformation of flattened chains which cannot form sufficient entanglements with free chains in the melt. Since the formation of flattened chains is rather general, the presented experimental findings not only shed new light on the interfacial interaction between free chains and flattened chains near the solids, but also provide a simple and effective way to control and manipulate the adhesive properties and crystallization behaviors of thin polymer films prepared on solid surfaces. On the other hand, the "loosely adsorbed" polymer chains, which are formed as a result of limited adsorption space on the solid surface, do display a degree of adhesion with the bulk polymer. We postulate that the loosely adsorbed chains act as "connectors" which promote adhesion effectively across the solid-polymer interface, while the "flattened" chains are so densely compact on the substrate that the outer free chains cannot penetrate into it to form adhesion.
dcterms.available2017-09-20T16:49:46Z
dcterms.contributorKoga, Tadanorien_US
dcterms.contributorSokolov, Jonathanen_US
dcterms.contributorKim, Taejin.en_US
dcterms.creatorChen, Zhizhao
dcterms.dateAccepted2017-09-20T16:49:46Z
dcterms.dateSubmitted2017-09-20T16:49:46Z
dcterms.descriptionDepartment of Materials Science and Engineeringen_US
dcterms.extent43 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/11401/76232
dcterms.issued2016-12-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:49:46Z (GMT). No. of bitstreams: 1 Chen_grad.sunysb_0771M_12875.pdf: 2083840 bytes, checksum: 81b2fc2c33ce49ebd0d22dee5324b8ea (MD5) Previous issue date: 42370en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectadhesion, flattened layer, interface, nanothin film, polymer
dcterms.titleNovel adhesion properties of irreversibly adsorbed polymer chains
dcterms.typeThesis


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