dc.creatorCARVALHO, Antonio C. S. M.
dc.creatorCHICOMA, Dennis L.
dc.creatorSAYER, Claudia
dc.creatorGIUDICI, Reinaldo
dc.date.accessioned2012-10-19T01:45:11Z
dc.date.accessioned2018-07-04T14:51:01Z
dc.date.available2012-10-19T01:45:11Z
dc.date.available2018-07-04T14:51:01Z
dc.date.created2012-10-19T01:45:11Z
dc.date.issued2010
dc.identifierINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, v.49, n.21, p.10262-10273, 2010
dc.identifier0888-5885
dc.identifierhttp://producao.usp.br/handle/BDPI/18511
dc.identifier10.1021/ie100422v
dc.identifierhttp://dx.doi.org/10.1021/ie100422v
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1615306
dc.description.abstractThis contribution describes the development of a continuous emulsion copolymerization processs for vinyl acetate and n-butyl acrylate in a tubular reactor. Special features of this reactor include the use of oscillatory (pulsed) flow and internals (sieve plates) to prevent polymer fouling and promote good radial mixing, along with a controlled amount of axial mixing. The copolymer system studied (vinyl acetate and butyl acrylate) is strongly prone to composition drift due to very different reactivity ratios. An axially dispersed plug flow model, based on classical free radical copolymerization kinetics, was developed for this process and used successfully to optimize the lateral feeding profile to reduce compositional drift. An energy balance was included in the model equations to predict the effect of temperature variations on the process. The model predictions were validated with experimental data for monomer conversion, copolymer composition, average particle size, and temperature measured along the reactor length.
dc.languageeng
dc.publisherAMER CHEMICAL SOC
dc.relationIndustrial & Engineering Chemistry Research
dc.rightsCopyright AMER CHEMICAL SOC
dc.rightsrestrictedAccess
dc.titleDevelopment of a Continuous Emulsion Copolymerization Process in a Tubular Reactor
dc.typeArtículos de revistas


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