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Polymer colloids for catalysis in fluorous media and for colloidal crystalline arrays

dc.contributor.advisorFord, Warren T.
dc.contributor.authorKarnati, Rangarani
dc.date.accessioned2013-11-26T08:21:26Z
dc.date.available2013-11-26T08:21:26Z
dc.date.issued2009-05
dc.identifier.urihttps://hdl.handle.net/11244/6456
dc.description.abstractScope and Method of Study: Monodisperse charged polymer colloids in aqueous and non-aqueous dispersions have potential applications as membranes and catalysts. We chose poly(methyl methacrylate) polymer particles for the catalytic and colloidal crystalline filter fabrication applications. Micron sized poly(ethylhexyl methacrylate) (EHMA) cross-linked copolymers in fluorinated solvents were synthesized by dispersion polymerization using microwave heating for the catalytic applications. Sub-micron sized poly(methyl methacrylate) (PMMA) core-shell latexes in aqueous media were made by emulsifier-free emulsion polymerization for colloidal crystal films (CCF) making.
dc.description.abstractFindings and Conclusions: Cationic EHMA copolymers slightly increased the hydrolysis of p-nitrophenyl hexanoate in fluorous media compared to the control experiment which lacked the polymer particles. PMMA CCF's fabricated by gravitational sedimentation method contained monodisperse FCC packed domains of 5-10 µm, point defects, and grain boundaries.
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dc.languageen_US
dc.rightsCopyright is held by the author who has granted the Oklahoma State University Library the non-exclusive right to share this material in its institutional repository. Contact Digital Library Services at lib-dls@okstate.edu or 405-744-9161 for the permission policy on the use, reproduction or distribution of this material.
dc.titlePolymer Colloids for Catalysis in Fluorous Media and for Colloidal Crystalline Arrays
dc.titlePolymer colloids for catalysis in fluorous media and for colloidal crystalline arrays
dc.contributor.committeeMemberBerlin, K. Darrell
dc.contributor.committeeMemberBunce, Richard A.
dc.contributor.committeeMemberSlaughter, LeGrande M.
dc.contributor.committeeMemberMatts, Robert L.
osu.filenameKarnati_okstate_0664D_10052.pdf
osu.accesstypeOpen Access
dc.type.genreDissertation
dc.type.materialText
thesis.degree.disciplineChemistry
thesis.degree.grantorOklahoma State University


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