Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/64734
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dc.titleThickness dependent thermal rearrangement of an ortho-functional polyimide
dc.contributor.authorWang, H.
dc.contributor.authorChung, T.-S.
dc.contributor.authorPaul, D.R.
dc.date.accessioned2014-06-17T07:50:42Z
dc.date.available2014-06-17T07:50:42Z
dc.date.issued2014-01-15
dc.identifier.citationWang, H., Chung, T.-S., Paul, D.R. (2014-01-15). Thickness dependent thermal rearrangement of an ortho-functional polyimide. Journal of Membrane Science 450 : 308-312. ScholarBank@NUS Repository.
dc.identifier.issn03767388
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64734
dc.description.abstractThe effect of film thickness on the thermal rearrangement of an ortho-functional polyimide, derived from 2,2'-bis-(3,4-dicarboxyphenyl) hexafluoropropane dianhydride (6FDA) and 3,3'-dihydroxy-4,4'-diamino-biphenyl (HAB), to a polybenzoxazole structure was explored over the range from 50. nm to 100. μm. The rate of thermal rearrangement of this ortho-functional polyimide was found to be strongly dependent on film thickness. A thin film of 56. nm experienced a much more rapid and extensive thermal rearrangement process than a thick film of 100. μm as tracked by thermogravimetric analysis, TGA. The conversion of the ortho-functional polyimide to polybenzoxazole commences at a lower temperature for thinner films than for thicker films. Isothermal TGA experiments at 370. °C showed a much larger weight loss, or extent of rearrangement, at a given time for thin films compared to thick films. These observations are believed to reflect greater chain segmental mobility in the thin films, due to the proximity of the free surfaces, and perhaps the reduced diffusional resistance for removal of the evolving volatile compounds accompanying the rearrangement reaction.© 2013 Elsevier B.V.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.memsci.2013.09.006
dc.sourceScopus
dc.subjectDiffusional resistance
dc.subjectPolymer segmental mobility
dc.subjectThermal rearrangement
dc.subjectThickness dependence
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.sourcetitleJournal of Membrane Science
dc.description.volume450
dc.description.page308-312
dc.description.codenJMESD
dc.identifier.isiut000326324600034
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