Influence of ion-exchange resin catalysts on side reactions of the esterification of n -Butanol with acetic acid
Kinetics of side reactions of the formation of n-butyl acetate in the heterogeneously catalyzed esterification of n-butanol with acetic acid were studied in an isothermal fixed-bed flow reactor at temperatures between 100 and 120 °C. The observed side reaction products are isomers of butene, di- n-b...
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Veröffentlicht in: | Chemical engineering science 2006, Vol.61 (2), p.753-765 |
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Sprache: | eng |
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Zusammenfassung: | Kinetics of side reactions of the formation of
n-butyl acetate in the heterogeneously catalyzed esterification of
n-butanol with acetic acid were studied in an isothermal fixed-bed flow reactor at temperatures between 100 and 120
°C. The observed side reaction products are isomers of butene, di-
n-butyl ether,
sec.-butyl-
n-butyl ether as well as
sec.-butanol and
sec.-butyl acetate. Three ion-exchange resin catalysts with a similar matrix but different sulfonation are compared:
Purolite
™
CT 269 is mono-sulfonated whereas
Amberlyst
™
46 is surface-sulfonated and
Amberlyst
™
48 is bi-sulfonated.
Purolite
™
CT 269 and
Amberlyst
™
48 are fully sulfonated in the gel phase, whereas
Amberlyst
™
46 is only surface-sulfonated. The ion-exchange capacities of
Purolite
™
CT 269 and
Amberlyst
™
48 are similar, that of
Amberlyst
™
46 is lower by a factor of 5. Despite this, all three catalysts show only minor differences in their activity regarding the esterification. Regarding the formation of side products,
Purolite
™
CT 269 and
Amberlyst
™
48 give similar results: side reactions proceed to significant extent. For
Amberlyst
™
46, however, side reactions were found to be almost negligible. It is concluded that the esterification occurs mainly on or near the external surface of catalysts particles whereas side reactions occur mainly in the pores. This work shows that surface-sulfonated catalysts like
Amberlyst
™
46 are very attractive for the production of esters by reactive distillation. |
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ISSN: | 0009-2509 1873-4405 |
DOI: | 10.1016/j.ces.2005.07.007 |