Reactive Distillation (RD) is a combination of reaction and distillation in a single unit
having a number of specific advantages over conventional sequential approach of reaction followed
by distillation or any other separation techniques. The combined effect of reaction and
separation increases the selectivity of the product and enhances the conversion of the reactant. The
RD unit provides better control and proper utilization of reaction heat. Moreover, easier
separation of the components can be achieved and formation of azeotropes can be avoided in the
RD column. The complex behavior of the RD column arises because of the complicated
vapor-liquid interactions, mass transfer between solid, liquid and vapor phases, intra-particle
(catalyst) diffusion in the case of catalyzed reactions, and reaction kinetics involved with
separation. Therefore, such kinds of multi directional interactions in the RD system lead to
multiple steady-states and complex dynamics (Taylor and Krishna, 2000).
Therefore, to understand the complete behavior of the simultaneous reaction
and separation process, research on various fields, like modeling and simulation, process
synthesis, column design, nonlinear Vapor-Liquid Equilibrium (VLE) behavior, and development
of control strategy, has been on. But the feasibility of the RD process for a particular
reaction may depend upon some of the important factors like relative volatilities of the
components involved in the reaction, column and reaction temperature, pressure, optimum reflux
ratio, etc. Hence, RD may not always be the choice for every chemical reaction. Hence,
substantial consideration to enlarge the domain of research on RD processes is required. |