Intro To Distillation
Intro To Distillation
Intro To Distillation
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
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
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
COLUMN INTERNALS
Trays and Plates
COLUMN INTERNALS
Trays and Plates
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
COLUMN REBOILERS
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
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
Simple Distillation
Fractional
Distillation
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.
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
separated
fractions
are
removed
Continuous binary
fractional distillation tower.
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
of the liquid ;
Overhead
Product
Heater
Separator
Bottom
Product
Flash Distillation
Flash Distillation
Features
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
Rayleigh Distillation
Vapor
x
i
L'
dxi
ln '
L0 xio yi xi
Heat
Liquid Charge
Rayleigh Distillation
(Contd)
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 )
- The End
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