Influence of unequal
component efficiencies on trajectories during distillation of a
homogeneous azeotropic mixture
J.A.
Ojeda Nava and R. Krishna
The overall objective of this work is to
examine the influence of interphase mass transfer on the composition
trajectories in homogeneous azeotropic distillation. A total of 38
experiments were carried out in a bubble cap distillation column
operated at total reflux with the system: water–ethanol–tert-butanol.
The experiments were carried out in the two
regions on either side of the distillation boundary connecting the
ethanol–water and t-butanol–water azeotropes. In order to model the
composition trajectories, a rigorous nonequilibrium (NEQ) stage model is
developed. The
NEQ model incorporates the Maxwell–Stefan diffusion equations to
describe the intraphase transfers in the vapor and liquid phases. The
only adjustable parameter in the NEQ model is the size of the vapor
bubbles on trays. A choice of a bubble
diameter of 4mm in the developed NEQ model gave the best agreement
with the experimental results for all of the 38 experimental runs. The
Murphree efficiencies of the constituents in the ternary mixture were
found to be significantly different from one another for all the runs.
In order to ascertain the influence of unequal component efficiencies on
the column composition trajectories, the experimental results were also
simulated with an equilibrium (EQ) stage model assuming a uniform,
constant efficiency for all components on all the trays. The value of
this constant efficiency for any experimental run was obtained by
averaging the individual component efficiencies for all the three
components on all the trays, calculated by the rigorous NEQ model. The
predictions of the EQ model leads to significantly worse predictions of
the column composition trajectories for each of the runs, when compared
to the NEQ model. It is found that the column composition trajectories
are significantly altered due to differences in the component
efficiencies. From a design view point, it is shown that for the
water–ethanol–tert-butanol system, the attainment of a desired
ethanol purity in the top product may require significantly larger
number of stages than that anticipated by the EQ model incorporating
constant component efficiencies.
Hydrodesulphurization of
gasoils: Advantages of counter- current gas-liquid contacting
J.A.
Ojeda, J. Ramirez and R. Krishna
Hydrodesulphurization
(HDS) of gasoils is conventionally carried out in the petroleum industry
in co-current trickle bed reactors.
The important disadvantage of co-current operation is that the
build-up of H2S along the reactor height is detrimental to
the desulphurisation reaction; this is because of inhibition effects.
In this paper we examine the benefits of carrying out the HDS
reaction in a counter-current mode. We carried out simulations of the
co- and counter-current configurations using an equilibrium
stage model and taking dibenzothiophene
(DBT) as a model sulphur compound. Our simulations show that
counter-current operation can significantly reduce the requirements
in the total amount of catalyst when ultra low levels of S are
demanded in the product steam. For the same amount of catalyst, the
conversion of DBT is significantly higher.
IN-SITU STRIPPING OF H2S
IN GASOIL HYDRODESULPHURIZATION: Reactor Design Considerations
J.
A. OJEDA NAVA and R. KRISHNA
In order to meet future diesel
specifications the sulphur content of diesel would need to be reduced to
below 50 ppm. This requirement would require improved reactor
configurations. In this study we examine the benefits of counter-current
contacting of gas oil with H2, over conventional co-current
contacting in a trickle bed hydrodesulphurization (HDS) reactor. In
counter-current contacting, we achieve in-situ stripping of H2S
from the liquid phase; this is beneficial to the HDS kinetics. A
comparison simulation study shows that counter-current contacting would
require about 20% lower catalyst load than co-current contacting.
However, counter-current contacting of gas and liquid phases in
conventionally used HDS catalysts, of 1.5mm sizes, is not possible due
to floooding limitations. The catalysts need to be housed in special
wire gauze envelopes as in the catalytic
bales or KATAPAK-S configurations. A preliminary hardware
design of a counter-current HDS reactor using catalytic bales was
carried out in order to determine the technical feasibility. Using a
realistic sulphur containing feedstock, the target of 50 ppm S content
of desulphurized oil could be met in a reactor of reasonable dimensions.
The study also underlines the need for accurate modelling of thermal
effects during desulphurization. Our study also shows that interphase
mass transfer is unlikely to be a limiting factor and there is a
need to develop improved reactor configurations allowing for increased
catalyst loading, at the expense of gas–liquid interfacial area.
COMBINING DISTILLATION AND
HETEROGENEOUS CATALYTIC REACTORS
J.
A. OJEDA NAVA, R. BAUR and R.
KRISHNA
The
hardware design of reactive distillation (RD) columns pose severe
challenges with respect to the choice and design of the hardware; the
requirements of reaction (i.e. high liquid or catalyst holdup) are not
in consonance with the requirement of separation (high interfacial
area). In this paper we examine an alternative to the RD concept, namely
a distillation column networked with a single side (external) reactor,
which we call the SR
concept. For the case study of tertiary-amyl ether (TAME) production
by reaction of isoamylene (IA) with methanol, we show that employing the
SR concept it is possible to meet the design
targets of IA conversion, TAME purity in bottom product and TAME
impurity in top product using just one side reactor. From detailed
hardware designs, we see that the RD column is significantly taller
than the distillation column in the SR configuration; this is due to the
placement of the catalyst load within the RD column. We conclude that
the SR concept will be competitive with the RD column configuration
provided the IA conversion targets are not too stringent. |