Separation Processes
Introduction to
Prepared by:
Engr. Rejie C. Magnaye
DISTILLATION
Distillation is defined as: a process in which a
liquid or vapour mixture of two or more
substances is separated into its component
fractions of desired purity, by the application
and removal of heat.
Although many people have a fair idea what
distillation means, the important aspects that seem
to be missed from the manufacturing point of view are
that:
distillation is the most common separation technique
because
it consumes enormous amounts of energy, both in
terms of cooling and heating requirements
Types of Distillation
Columns
Batch Columns In batch operation, the feed to the
column is introduced batch-wise. That is, the column
is charged with a 'batch' and then the distillation
process is carried out. When the desired task is
achieved, a next batch of feed is introduced.
Continuous Columns In contrast, continuous
columns process a continuous feed stream. No
interruptions occur unless there is a problem with the
column or surrounding process units. They are
capable of handling high throughputs and are the
most common of the two types. We shall concentrate
only on this class of columns.
Types of Continuous
Columns
a. the nature of the feed that they are processing,
binary column - feed contains only two components
multi-component column - feed contains more than two
components
b. the number of product streams they have
multi-product column - column has more than two product
stream
c. where the extra feed exits when it is used to help with
the separation,
extractive distillation - where the extra feed appears in the
bottom product
stream
azeotropic distillation - where the extra feed appears at the
top product stream
d. the type of column internals
tray column - where trays of various designs are used to hold
BASIC DISTILLATION
EQUIPMENT AND OPERATION
Main Components of Distillation
Columns
a vertical shell where the
separation of liquid components is
carried out
column internals such as
trays/plates and/or packings
which are used to enhance
component separations
a reboiler to provide the
necessary vaporisation for the
distillation process
a condenser to cool and condense
the vapour leaving the top of the
column
a reflux drum to hold the
condensed vapour from the top of
the column so that liquid (reflux)
can be recycled back to the
column
Basic Operation and
Terminology
Feed the liquid mixture that is to
be processed and this is introduced
usually somewhere near the middle
of the column to a tray known as the
feed tray.
The feed tray divides the column
into a top (enriching or rectification)
section and a bottom (stripping)
section. The feed flows down the
column where it is collected at the
bottom in the reboiler. Heat is
supplied to the reboiler to generate
vapour.
The vapour raised in the reboiler is
Basic Operation and
Terminology
The vapour moves up the column, and as it exits the top of the
unit, it is cooled by a condenser. The condensed liquid is stored
in a holding vessel known as the reflux drum. Some of this
liquid is recycled back to the top of the column and this is
called the reflux. The condensed liquid that is removed from
the system is known as the distillate or top product.
Thus, there are internal flows of vapour and liquid within the
column as well as external flows of feeds and product streams,
into and out of the column.
COLUMN INTERNALS
Trays and Plates
Bubble cap trays. A bubble
cap tray has riser or chimney
fitted over each hole, and a
cap that covers the riser. The
cap is mounted so that there
is a space between riser and
cap to allow the passage of
vapour. Vapour rises through
the chimney and is directed
downward by the cap, finally
discharging through slots in
COLUMN INTERNALS
Trays and Plates
Valve trays. In valve trays,
perforations are covered by
liftable caps. Vapour flows
lifts the caps, thus self
creating a flow area for the
passage of vapour. The lifting
cap directs the vapour to
flow horizontally into the
liquid, thus providing better
mixing than is possible in
sieve trays.
COLUMN INTERNALS
Trays and Plates
Sieve trays .Sieve trays
are simply metal plates with
holes in them. Vapour
passes straight upward
through the liquid on the
plate. The arrangement,
number and size of the
holes are design
parameters.
Tray Designs
A tray essentially acts as a minicolumn, each accomplishing a fraction
of the separation task. From this we
can deduce that the more trays there
are, the better the degree of
separation and that overall separation
efficiency will depend significantly on
the design of the tray. Trays are
designed to maximise vapour-liquid
contact by considering the liquid
distribution and vapour distribution on
the tray. This is because better vapourliquid contact means better separation
at each tray, translating to better
Packings
Packings are passive devices that are
designed to increase the interfacial
area for vapour-liquid contact.
COLUMN REBOILERS
There are a number of designs of reboilers. They
can be regarded as heat-exchangers that are
required to transfer enough energy to bring the
liquid at the bottom of the column to boiling boint.
The following are examples of typical reboiler
types.
COLUMN REBOILERS
Tube Bundle
DISTILLATION PRINCIPLES
Separation of components from a liquid mixture via distillation
depends on the differences in boiling points of the individual
components. Also, depending on the concentrations of the
components present, the liquid mixture will have different
boiling point characteristics. Therefore, distillation processes
depends on the vapour pressure characteristics of liquid
Vapour
Pressure and Boiling
mixtures.
energy input raises vapour pressure
vapour pressure is related to boiling
a liquid is said to boil when its vapour pressure equals the
surrounding pressure
the ease with which a liquid boils depends on its volatility
liquids with high vapour pressures (volatile liquids) will boil at
lower temperatures
the vapour pressure and hence the boiling point of a liquid
mixture depends on the relative amounts of the components in the
mixture
The Boiling Point Diagram
The dew-point is the
temperature at which
the saturated vapour
starts to condense.
The bubble-point is the
temperature at which
the liquid starts to boil.
The region above the dewpoint curve shows the
equilibrium composition of
the superheated vapour
while the region below the
bubble-point curve shows
the equilibrium composition
Relative Volatility
Relative volatility is a measure of the
differences in volatility between 2
components, and hence their boiling
points. It indicates how easy or
difficult a particular separation will be.
The relative volatility of component i
with respect to component j is
defined as
yi = mole fraction of component i
in the vapour
xi = mole fraction of component i
in the liquid
Vapor Liquid Equilbria
Distillation columns are designed
based on the boiling point properties
of the components in the mixtures
being separated. Thus the sizes,
particularly the height, of distillation
columns are determined by the
vapour liquid equilibrium (VLE) data
for the mixtures.
Vapor Liquid Equilbrium
Curves
Constant pressure VLE
data is obtained from
boiling point diagrams.
VLE data of binary
mixtures is often
presented as a plot, as
shown in the figure on
the right. The VLE plot
expresses the bubblepoint and the dew-point
of a binary mixture at
constant pressure. The
curved line is called the
equilibrium line and
Vapor Liquid Equilbrium
Curves
An azeotrope is a liquid mixture which when
vaporised, produces the same composition as the
liquid. The two VLE plots below, show two different
azeotropic systems, one with a minimum boiling point
and one with a maximum boiling point. In both plots,
the equilibrium curves cross the diagonal lines, and this
are azeotropic points where the azeotropes occur. In
other words azeotropic systems give rise to VLE plots
where the equilibrium curves crosses the diagonals.
Vapor Liquid Equilbrium
Curves
The design procedure is simple. Given
the VLE diagram of the binary mixture,
operating lines are drawn first. Operating
lines define the mass balance relationships
between the liquid and vapour phases in
the column. There is one operating line for
the bottom (stripping) section of the
column, and on for the top (rectification or
enriching) section of the column. Use of the
constant molar overflow assumption also
ensures the the operating lines are straight
Simple Distillation
In simple distillation, all
the hot vapors produced
are
immediately
channeled
into
a
condenser which cools and
condenses the vapors.
Therefore, the distillate
will not be pure its
composition
will
be
identical
to
the
composition of the vapors
at the given temperature
and pressure.
Fractional
Distillation
For many cases, the boiling
points of the components in
the
mixture
will
be
sufficiently
close
that
Raoult's law must be taken
into consideration.
Therefore,
fractional
distillation must be used in
order
to
separate
the
components
well
by
repeated
vaporizationContinuous fractional distillation
condensation cycles within
tower separating one feed mixture
packed
fractionating
stream into four distillate and one a
bottoms fractions
column.
Batch Distillation
In differential distillation a feed
mixture (an initial charge) of a
given composition is placed in
a single stage separator and
heated to boiling. The vapor is
collected and condensed to a
distillate. The composition of
the remaining liquid and the
distillate are functions of time.
Reasons for running a batch process
1)
Small
capacity
doesnt
warrant
continuous
operation
2) Separation is to be done only occasionally
3) Separation is preparative to produce a new product
4) Upstream operations are batch-wise or feed-stocks
vary with time or from batch to batch
5) Feed materials are not appropriate for a continuous
flow system
Continuous distillation
A mixture is continuously fed into the process
and
separated
fractions
are
removed
continuously as output streams as time passes
during the operation.
In practice when there are multiple distillate
fractions, each of the distillate exit points is
located at different heights on a fractionating
column. The bottoms fraction can be taken
from the bottom of the distillation column or
unit, but is often taken from a reboiler
Continuous binary
fractional distillation tower.
Continuous fractional distillation
tower separating one feed mixture
stream into four distillate and one
bottoms fractions
Flash Distillation
Equilibrium distillation (Flash distillation) is a single
stage separation technique. A liquid mixture feed is
pumped through a heater to raise the temperature
of the mixture. It then flows through a valve and the
pressure is reduced, causing the liquid to partially
vaporize. Once the mixture enters a big enough
volume, the liquid and vapor separate.
Because the vapor and
liquid are in such close
contact up until the "flash"
occurs, the product liquid
and
vapor
phases
approach equilibrium.
Flash Distillation
The flash distillation process
Condenser
consists of three parts.
a. Vaporizing a definite fraction
Throttle
of the liquid ;
c. Condensing the vapor.
Overhead
Product
Heater
b. Separating the vapor from the
liquid;
Separator
Bottom
Product
Flash Distillation
Flash Distillation
Features
a. Continuous steady state
Operating conditions (T & P)
Condenser
are constant.
b. Compositions & flow rates of
feed , products of overhead
and bottom are constant
c. There is equilibrium always
Throttle
Separator
Overhead
Product
Heater
Bottom
Product
between phases of vapor and liquid .
Flash Distillation
Rayleigh Distillation
Vapor
x
i
L'
dxi
ln '
L0 xio yi xi
Heat
Liquid Charge
L, xi remaining liquid and mole fraction at any subsequent time
L0, xi0 initial liquid amount and mole fraction
Rayleigh Distillation
(Contd)
For binary mixture when ij is constant
y i / xi
ij
yj / xj
yi
ij .xi
1 ( ij 1).xi
L'
ln '
L0
xi (1 xi 0 )
1 xi 0
1
ln
ln
1 xi
ij 1 xi 0 (1 xi )
Video Clip Presentation
CRUDE OIL DISTILLATION
PART I
CRUDE OIL DISTILLATION PART II
- The End
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