Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/58272
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dc.contributor.authorMeena, M-
dc.contributor.authorUmapathy, M J-
dc.contributor.authorYoganand, K S-
dc.date.accessioned2021-10-13T06:27:32Z-
dc.date.available2021-10-13T06:27:32Z-
dc.date.issued2021-07-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/58272-
dc.description445-452en_US
dc.description.abstractIn the present kinetic study, glycidyl methacrylate has been polymerized using synthesized single-site phase transfer catalyst - 2-benzoylethyldecyldimethylammonium bromide and di-site –phase transfer catalyst -1,1,4,4-tetramethyl-1,4 dioctylethylenediammonium bromide along with potassium peroxydisulfate as the initiator in inert medium and at a constant temperature of 60°C. The effect of concentrations of the monomer, initiator, catalyst, ionic strength, pH and solvent polarity on the rate of polymerization has been examined. The order with respect to the monomer, initiator, and phase transfer catalyst was found to be 1, 0.5, and 0.5, respectively. A suitable polymerization mechanism is proposed. Ionic strength and pH has no impact on the rate of polymerization. It is observed that, as the solvent's polarity increased, the rate of polymerization also increased. Di-site phase transfer catalyst results in a higher rate of polymerization compared with single-site phase transfer catalyst while polymerizing glycidyl methacrylate.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJCT Vol.28(4) [July 2021]en_US
dc.subjectFree Radical Polymerizationen_US
dc.subjectKineticsen_US
dc.subjectMechanismen_US
dc.subjectPhase Transfer Catalysten_US
dc.subjectRate of Polymerizationen_US
dc.titleEfficiency of single and di- site phase transfer catalyzed polymerization of glycidyl methacrylate in the two-phase system: A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.28(4) [July 2021]

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