Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/94570
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dc.titlePolymerization of methyl methacrylate in ternary systems: Emulsion and microemulsion
dc.contributor.authorGan, L.M.
dc.contributor.authorChew, C.H.
dc.contributor.authorNg, S.C.
dc.contributor.authorLoh, S.E.
dc.date.accessioned2014-10-16T08:37:34Z
dc.date.available2014-10-16T08:37:34Z
dc.date.issued1993
dc.identifier.citationGan, L.M.,Chew, C.H.,Ng, S.C.,Loh, S.E. (1993). Polymerization of methyl methacrylate in ternary systems: Emulsion and microemulsion. Langmuir 9 (11) : 2799-2803. ScholarBank@NUS Repository.
dc.identifier.issn07437463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94570
dc.description.abstractThe ternary systems containing water, methyl methacrylate (MMA), and cetyltrimethylammonium bromide (CTAB) could be continuously changed from turbid emulsions to transparent microemulsions by merely increasing the surfactant concentration. Stable PMMA latexes (16-30 nm in hydrodynamic radius) were obtained from emulsion and microemulsion polymerizations initiated by potassium persulfate (KPS). Molecular weights of PMMA were in the range of (5 to 7) × 106. The activation energies of the polymerizations for both systems were about the same (81 and 85 kJ mol-1). Each latex particle containing about one to two polymer chains was obtained from microemulsion polymerization of 5 wt % MMA while it was about four from emulsion polymerization at the same MMA concentration. The number of polymer chains per latex particle increased to about five for microemulsions and nine for emulsions at 9 wt % MMA. The low dependency of polymerization rate on [CTAB]0.31 and its strong dependency on [KPS]0.82 were observed for emulsion polymerizations in contrast with [CTAB]0.58 and [KPS]0.33 for microemulsion polymerizations. The possible polymerization mechanisms related to micellar nucleation, homogeneous nucleation, and monomer droplet initiation are discussed. © 1993 American Chemical Society.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleLangmuir
dc.description.volume9
dc.description.issue11
dc.description.page2799-2803
dc.identifier.isiutNOT_IN_WOS
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