Please use this identifier to cite or link to this item: https://doi.org/10.1002/app.1991.070431106
DC FieldValue
dc.titleDynamic mechanical analysis of tropical wood-polymer composites
dc.contributor.authorYap, M.G.S.
dc.contributor.authorQue, Y.T.
dc.contributor.authorChia, L.H.L.
dc.date.accessioned2014-05-16T07:36:41Z
dc.date.available2014-05-16T07:36:41Z
dc.date.issued1991-12-05
dc.identifier.citationYap, M.G.S., Que, Y.T., Chia, L.H.L. (1991-12-05). Dynamic mechanical analysis of tropical wood-polymer composites. Journal of Applied Polymer Science 43 (11) : 1999-2004. ScholarBank@NUS Repository. https://doi.org/10.1002/app.1991.070431106
dc.identifier.issn00218995
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/52693
dc.description.abstractWood-polymer composites (WPC) of Geronggang (GE; Cratoxylon arborescens), a light tropical hardwood, impregnated with methyl methacrylate (MMA) and styrene-co-acrylonitrile (3:2; STAN), were prepared by in situ polymerization using γ radiation or catalyst-heat treatment. The dynamic flexural storage modulus, E′, for oven-dried GE, moist GE, and GE-MMA and GE-STAN composites decreased with increasing temperature. The percentage decreases for GE with 10 and 16.5% moisture contents were 74.5 and 98.2%, respectively, which were higher than those for GE and GE composites, which ranged between 40 and 50%. The impregnated polymers were not as effective as water in acting as plasticizers, due to their nonpolar nature and much higher molecular weights. The α-transition peaks for moist GE and GE composites were more distinct and were shifted to lower temperatures than those for oven-dried GE. The values ranged between 75 and 150°C for moist GE and between 102 and 170°C for the GE composites. The α-transitions of the catalyst-heat-treated GE composites were lower than that of the radiation-induced counterparts. GE-STAN composites were also observed to have lower α-transition temperatures than those for GE-MMA for the respective treatment process, which seems to suggest that STAN interacted to a greater extent with cell wall components than did MMA.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/app.1991.070431106
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentCHEMICAL ENGINEERING
dc.description.doi10.1002/app.1991.070431106
dc.description.sourcetitleJournal of Applied Polymer Science
dc.description.volume43
dc.description.issue11
dc.description.page1999-2004
dc.description.codenJAPNA
dc.identifier.isiutA1991GQ23600006
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