In this work, the kinetics and equilibrium of the heterogeneously catalyzed liquid-phase formation of tert -amyl ethyl ether (TAEE) were studied. The catalyst used was a commercial sulfonic acid ion-exchange resin (Amberlyst 16W). The experiments were carried out in a continuous stirred-tank reactor, measuring stationary reaction rates. The measured reaction rates were fitted to three kinetic models; homogeneous, Eley−Rideal type, and Langmuir−Hinshelwood type. Of these, the Langmuir−Hinshelwood type model described the experimental results best. This model is based on single-site adsorption of every component, with the surface reaction being the rate-limiting step. The activation energies for the formation of tert -amyl ethyl ether from 2-methyl-1-butene were 90 and from 2-methyl-2-butene 108 kJ·mol - 1 . For the isomerization of 2-methyl-1-butene to 2-methyl-2-butene, an activation energy of 82 kJ·mol - 1 was obtained.
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Linnekoski et al. (1997) studied this question.
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