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dc.contributor.authorLee, Ting-Hsienen_US
dc.contributor.authorChiu, Yu-Jingen_US
dc.contributor.authorLai, Yu-Chengen_US
dc.contributor.authorFan, Ping-Wenen_US
dc.contributor.authorKuo, Tyng-Yowen_US
dc.contributor.authorLiau, Ianen_US
dc.contributor.authorChen, Jiun-Taien_US
dc.date.accessioned2015-07-21T11:20:39Z-
dc.date.available2015-07-21T11:20:39Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c4ra06228ken_US
dc.identifier.urihttp://hdl.handle.net/11536/124008-
dc.description.abstractElectrospinning is one of the most common methods to prepare polymer fibers with sizes ranging from several nanometers to hundreds of micrometers. In most studies of electrospun polymer fibers, the properties and morphologies of polymer fibers are controlled by changing the electrospinning conditions. Few studies focus on the post-treatments of polymer fibers, which are critical for many fiber-based applications. In this work, we investigate the morphology transformation of electrospun polystyrene (PS) fibers annealed on top of poly(methyl methacrylate) (PMMA) film-coated glass substrates. In situ optical microscopy and stimulated Raman scattering (SRS) microscopy are used to observe the transformation process, which is driven by the Rayleigh instability, the surface tensions, and the interfacial tensions of polymers. Depending on the thickness of the underlying PMMA films, the electrospun PS fibers may transform into hemispheres or disks. The growth rates of the undulating amplitude are also affected by the film thickness.en_US
dc.language.isoen_USen_US
dc.titleRayleigh-instability-driven morphology transformation of electrospun polymer fibers imaged by in situ optical microscopy and stimulated Raman scattering microscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c4ra06228ken_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.issue94en_US
dc.citation.spage51884en_US
dc.citation.epage51892en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000344389000007en_US
dc.citation.woscount0en_US
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