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dc.contributor.authorNATARAJAN, Uen_US
dc.contributor.authorHANDIQUE, Ken_US
dc.contributor.authorMEHRA, Aen_US
dc.contributor.authorBELLARE, JRen_US
dc.contributor.authorKHILAR, KCen_US
dc.date.accessioned2011-07-15T03:26:03Zen_US
dc.date.accessioned2011-12-26T12:49:13Zen_US
dc.date.accessioned2011-12-27T05:35:01Z
dc.date.available2011-07-15T03:26:03Zen_US
dc.date.available2011-12-26T12:49:13Zen_US
dc.date.available2011-12-27T05:35:01Z
dc.date.issued1996en_US
dc.identifier.citationLANGMUIR, 12(11), 2670-2678en_US
dc.identifier.issn0743-7463en_US
dc.identifier.urihttp://dx.doi.org/10.1021/la940584gen_US
dc.identifier.urihttp://dspace.library.iitb.ac.in/xmlui/handle/10054/4143en_US
dc.identifier.urihttp://hdl.handle.net/10054/4143
dc.description.abstractA modeling approach is developed to account for the important effects of intermicellar exchange on the ultrafine particle formation in reverse micelles. A set of fusion-fission schemes is specifically proposed and used for modeling intermicellar metal exchange. The dynamic effects largely differing in their time scales are decoupled using a two-staged approach. Growth of metal particles is simulated to occur through intramicellar attachment of free metal atoms from an instantaneous reduction reaction and as well as by transfer and attachment through intermicellar exchange. Simulation results predict increase in particle size with aqueous core size and total aqueous phase volume, increase in particle number density with surfactant concentration at fixed aqueous phase to surfactant molar ratio, a minimum in average particle size as a function of salt concentration, and increase in particle size polydispersity with salt concentration and aqueous core size. Low values of the order of 10(-1) are found for the number ratio of particles to micelles. All these effects have been observed experimentally. The mean core size and the critical metal nucleation number are found to be the primary influencing parameters for the final particle sizes. It is further found that the polydispersity can be controlled through proper choice of starting mixture conditions.en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectCadmium-Sulfide Insituen_US
dc.subjectMicro-Emulsionsen_US
dc.subjectPyrene Fluorescenceen_US
dc.subjectOil Microemulsionsen_US
dc.subjectInverted Micellesen_US
dc.subjectKinetic-Modelen_US
dc.subjectWateren_US
dc.subjectMediaen_US
dc.titleUltrafine metal particle formation in reverse micellar systems: Effects of intermicellar exchange on the formation of particlesen_US
dc.typeArticleen_US


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