Reactive Distillation

Reactive distillation
Binous - Reactive Distillation 1

Let us begin by considering a reversible reaction scheme: A+B ↔
C+D where the boiling points of the components follow the
sequence A, C, D and B.
The traditional flow-sheet for this process consists of a reactor

followed by a sequence of distillation columns.
The RD column consists of a reactive section in the middle with

nonreactive rectifying and stripping sections at the top and
bottom. The task of the rectifying section is to recover reactant B
from the product stream C. In the stripping section, the reactant
A is stripped from the product stream
Binous - Reactive D.
Distillation 3
The most spectacular example of the benefits of RD is in the
production of methyl acetate.
The acid catalyzed reaction MeOH+AcO ↔ MeOAc+H2O was

traditionally carried out using the processing scheme
consisting of one reactor and a train of nine distillation
columns.
In the RD implementation only one column is required and

nearly 100% conversion of the reactant is achieved. The capital
and operating costs are significantly reduced.
(a) Reactive distillation concept for synthesis of MTBE from the acid-catalysed
reaction between MeOH and iso-butene. The butene feed is a mixture of
reactive iso-butene and non-reactive n-butene.
(b) Reactive distillation concept for the hydration of ethylene oxide to

ethylene-glycol.
(c) Reactive distillation concept for reaction between benzene and propene to
form cumene.
(d) Reactive distillation concept for reaction production of propylene oxide

from propylene chlorohydrin and lime. The reactive sections are indicated by
grid lines.

Co-current gas-liquid downflow trickle-bed reactors are widely
applied for hydroprocessing of heavy oils. This co-current mode
of operation is disadvantageous in most hydroprocesses. This is
because reactions such as hydrodesulphurisation and
hydrogenation are inhibited by hydrogen sulphide formed.
The situation is clearly more favorable in the counter-current

mode of operation since in this case the major part of the bed
operates in the H2S lean regime.

(a) Simplification or elimination of the separation system can lead
to significant capital savings.
(b) Improved conversion of reactant approaching 100%. This

increase in conversion gives a benefit in reduced recycle costs.
(c) Improved selectivity. Removing one of the products from the

reaction mixture or maintaining a low concentration of one of the
reagents can lead to reduction of the rates of side reactions and
hence improved selectivity for the desired products.

(d) Significantly reduced catalyst requirement for the same degree
of conversion.
(e) Avoidance of azeotropes. RD is particularly advantageous when

the reactor product is a mixture of species that can form several
azeotropes with each other. RD conditions can allow the
azeotropes to be reacted away in a single vessel.
(f) Reduced by-product formation.

(g) Heat integration benefits. If the reaction is exothermic, the
heat of reaction can be used to provide the heat of vaporisation
and reduce the reboiler duty.
(h) Avoidance of hot spots and runaways using liquid vaporisation

as thermal fly wheel.

(a) Volatility constraints. The reagents and products must have suitable
volatility to maintain high concentrations of reactants and low
concentrations of products in the reaction zone.
(b) Residence time requirement. If the residence time for the reaction is
long, a large column size and large tray hold-ups will be needed and it may
be more economic to use a reactor-separator arrangement.
(c) Scale up to large flows. It is difficult to design RD processes for very large
flow rates because of liquid distribution problems in packed RD columns.
(d) Process conditions mismatch. In some processes the optimum

conditions of temperature and pressure for distillation may be far from
optimal for reaction and vice versa.

Counter-current vapor-liquid contacting in trayed columns

Counter-current vapor-liquid contacting in packed columns

Bubble regime
Decreasing Increasing
vapor flow Foam regime vapor flow
rates rates
Froth regime
Spray regime

Bubble regime: Regime undesirable in commercial applications
Foam regime: Regime at gas flow rates too low for most industrial
applications
Froth regime: Usual regime in commercial applications
Spray regime: Regime undesirable in commercial applications

The froth regime is usually to be preferred on the trays because of the desire to
maintain high liquid hold-up on the trays. High liquid hold-ups could be realised by
use of bubble caps, reverse flow trays with additional sumps to provide ample tray
residence time.
In the Eastman process for methyl acetate manufacture specially designed high liquid
hold-up trays are used.
Various tea-bag configurations. Catalyst particles need to be
enveloped in wire gauze packings and placed inside RD columns

Horizontally disposed (a) wire gauze gutters
and (b) wire gauze tubes containing catalyst.

Structured catalyst-sandwiches
Counter-current vapor-liquid-catalyst contacting in trayed columns. (a) catalyst in
envelopes inside downcomers, (b) tray contacting with catalyst placed in wire gauze
envelopes near the liquid exit from the downcomers and (c) alternating packed layers of
catalyst and trays.

Reactive distillation concept for
synthesis of MTBE from the acid-
catalysed reaction between
MeOH and iso-butene. The
butene feed is a mixture of
reactive iso-butene and non-
reactive n-butene.

Separation of close-boiling mixtures


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Reactive distillation

Binous - Reactive Distillation 1

The traditional flow-sheet for this process consists of a reactor

The RD column consists of a reactive section in the middle with

The acid catalyzed reaction MeOH+AcO ↔ MeOAc+H2O was

In the RD implementation only one column is required and

(b) Reactive distillation concept for the hydration of ethylene oxide to

(d) Reactive distillation concept for reaction production of propylene oxide

Binous - Reactive Distillation 7

The situation is clearly more favorable in the counter-current

Binous - Reactive Distillation 9

(b) Improved conversion of reactant approaching 100%. This

(c) Improved selectivity. Removing one of the products from the

Binous - Reactive Distillation 10

(e) Avoidance of azeotropes. RD is particularly advantageous when

(f) Reduced by-product formation.

Binous - Reactive Distillation 11

(h) Avoidance of hot spots and runaways using liquid vaporisation

Binous - Reactive Distillation 12

(d) Process conditions mismatch. In some processes the optimum

Binous - Reactive Distillation 13

Binous - Reactive Distillation 14

Binous - Reactive Distillation 15

Binous - Reactive Distillation 16

Froth regime: Usual regime in commercial applications

Spray regime: Regime undesirable in commercial applications

Binous - Reactive Distillation 17

Binous - Reactive Distillation 19

Binous - Reactive Distillation 20

Binous - Reactive Distillation 24

Binous - Reactive Distillation 25

Binous - Reactive Distillation 26

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