dc.creatorBarboza, M
dc.creatorHokka, CO
dc.creatorMaugeri, F
dc.date2002
dc.dateSEP
dc.date2014-11-16T18:27:41Z
dc.date2015-11-26T17:26:09Z
dc.date2014-11-16T18:27:41Z
dc.date2015-11-26T17:26:09Z
dc.date.accessioned2018-03-29T00:13:21Z
dc.date.available2018-03-29T00:13:21Z
dc.identifierBioprocess And Biosystems Engineering. Springer-verlag, v. 25, n. 3, n. 193, n. 203, 2002.
dc.identifier1615-7591
dc.identifierWOS:000178915900008
dc.identifier10.1007/s00449-002-0294-9
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/56950
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/56950
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/56950
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1284490
dc.descriptionA mathematical kinetic model for the adsorption and desorption of cephalosporin C on Amberlite XAD-2 resin is proposed. The model can represent Langmuir, Freundlich or linear isotherms at equilibrium. The intrinsic kinetic parameters and adsorption isotherms as well as physical parameters such as the effective diffusivity and the external mass transfer coefficient were obtained at different temperatures and ethanol concentrations. An unfavourable cephalosporin C adsorption occurred when ethanol was present in the solution. It has been shown that at 25degreesC the ethanol, at concentrations from 1.5% to 2.5%, decreases the cephalosporin C adsorption. However, this behaviour was not observed at 10degreesC. The kinetic model fitted the experimental data well under different conditions. The model was validated in a continuous process of cephalosporin C purification using the same resin. The model with the validated parameters is able to predict the behaviour of the reactor system. The continuous process is composed of two stirred tank reactors with adsorber recycle. The adsorption occurs in the first stage, and elution of the product takes place in the second stage with ethanol as eluent. The dynamic behaviour of the process was described using the following parameters: hydraulic residence time for the first (theta(h1)) and second stage (theta(h2)), solid residence time (theta(s)), initial concentration of CPC (C-0), inlet ethanol concentration (C-ET0) and kinetics parameters.
dc.description25
dc.description3
dc.description193
dc.description203
dc.languageen
dc.publisherSpringer-verlag
dc.publisherNew York
dc.publisherEUA
dc.relationBioprocess And Biosystems Engineering
dc.relationBioprocess. Biosyst. Eng.
dc.rightsfechado
dc.rightshttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dc.sourceWeb of Science
dc.subjectcontinuous purification
dc.subjectcephalosporin C purification
dc.subjectdynamic modelling
dc.subjectcephalosporin adsorption
dc.subjectPolymeric Sorbents
dc.subjectRecycle Extraction
dc.subjectAdsorption
dc.subjectSeparation
dc.subjectAntibiotics
dc.titleContinuous cephalosporin C purification: dynamic modelling and parameter validation
dc.typeArtículos de revistas


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