Reactive distillation has been demonstrated to reduce the capital cost
and increase reactant conversion in MTBE production. These advantages
are potentially transferable to the production of ETBE, TAME, and oth
er tertiary ethers. However, the design of reactive distillation colum
ns is complicated by interaction between phase and reaction equilibriu
m. Whereas in conventional distillation, an increase in fractionation
is always associated with an improvement in process performance (separ
ation of key components), the same does not necessarily apply to react
ive distillation. Using the production of ETBE as an example, several
reactive distillation columns were designed for various feed compositi
ons and design philosophies. It was found that the best designs incorp
orated high reflux ratios with a restricted number of theoretical stag
es, and that increasing the number of theoretical stages could actuall
y be detrimental to process performance.