Equilibrium conversion, selectivity and yield optimization of the simultaneous liquid-phase etherification of isobutene and isoamylenes with ethanol over Amberlyst 35

A prospective study on the product distribution at chemical equilibrium for the simultaneous liquid-phase etherification of isobutene and isoamylenes with ethanol over Amberlyst¿ 35 is presented. Experiments were performed isothermally in a 200 cm3 stirred tank batch reactor operating at 2.0 MPa. In...

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Detalles Bibliográficos
Autores: Soto López, Rodrigo, Fité Piquer, Carles, Ramírez Rangel, Eliana, Bringué Tomàs, Roger, Cunill García, Fidel
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2015
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/67738
Acceso en línea:https://hdl.handle.net/2445/67738
Access Level:acceso abierto
Palabra clave:Èters
Alquens
Alcohols
Oxidació
Equilibri químic
Ethers
Alkenes
Oxidation
Chemical equilibrium
Descripción
Sumario:A prospective study on the product distribution at chemical equilibrium for the simultaneous liquid-phase etherification of isobutene and isoamylenes with ethanol over Amberlyst¿ 35 is presented. Experiments were performed isothermally in a 200 cm3 stirred tank batch reactor operating at 2.0 MPa. Initial molar ratios of alcohol/olefins and isobutene/isoamylenes ranged both from 0.5 to 2, and temperature from 323 to 353 K. Reactants equilibrium conversion, selectivities and yields toward products were clearly affected by the experimental conditions. Experimental etherification yields have been modeled using the response surface methodology (RSM), combined with the stepwise regression method to include only the statistically significant variables into the model. The multiobjective optimization (MOO) of etherification yields has been carried out numerically, by means of the desirability function approach, and graphically, by using the overlaid contour plots (OCP). Optimal conditions for the simultaneous production of ethyl tert-butyl ether (ETBE) and tert-amyl ethyl ether (TAEE) have been found to be at low temperatures (323 to 337 K) and initial molar ratio alcohol/olefins close to 0.9 and isobutene/isoamylenes close to 0.5.