Distillation

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The McCabe Thiele

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Graphical Design
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Method
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Gavin Duffy
School of Electrical Engineering Systems
DIT Kevin St
Learning Outcomes
After this lecture you should be able to…..
•Explain the importance of Reflux
•Apply the McCabe Thiele graphical design method to
determine the number of equilibrium stages in a column
•Describe column internals (trays and packing)
•Define tray efficiency
•Explain the height of packing equivalent to a theoretical
plate
Thanks to Ming Tham’s website for pictures and
information. An excellent presentation on distillation:
http://lorien.ncl.ac.uk/ming/distil/copydist.htm
 Design Illustrated
slope=R/(R+1) 1. Obtain VLE curve
1.0
slope= (VB +1) /VB
2. Pick distillate composition,
0.9 XD, and Reflux ratio, R, and draw
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operating line for rectification
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5 3. Pick bottoms composition, XB,
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4 and Boilup ratio, VB, and draw
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operating line for stripping
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4. Start stepping off from the
0.4 distillate end until the
XD/(R+1) 2
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intersection of the two operating
lines is passed.
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5. Continue stepping but use the
0.1 1 stripping operating line
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6. Count the number of stages
0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0

XB Xa 7. Subtract one for the reboiler to

XD
give the number of theoretical
trays (or leave as safety factor)
Reflux Considerations
R= Flow returned as Reflux
Flow of top product taken off
The rectifying operating line slope depends on R.
Therefore, the number of stages required for a given
separation depends on R.
Effective reflux ratio can be greater than R if the column is
poorly insulated and may be subject to change due to
weather conditions. A well lagged column is more
consistent.
The amount of reflux lies somewhere between the two
extremes of total reflux and minimum reflux
Reflux Considerations
The two extremes are Total Reflux and Minimum Reflux
Total Reflux - all condensate is returned, no product is taken
off and no feed added.
This gives the minimum number of stages to achieve the
separation.
Minimum Reflux - reducing R requires more stages to
achieve the separation. Further reduction creates a pinch
point where an infinite number of stages is required.
Minimum reflux happens when the intersection of the
operating lines lies on the equilibrium curve
Total Reflux

All vapour is condensed and returned as liquid

Minimum number of plates

Can use Fenske equation to calculate Nmin

 xD (1 − xB ) 
ln 
 xB (1 − xD ) 
N min = −1
ln α

(Ref. Unit Operations, McCabe Smith, 6th ed. p666)

Sometimes a column is operated in total reflux at
startup
Minimum Reflux
Min Reflux happens when the two operating lines intersect on
equilibrium curve
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XB Xa
XD
Minimum Reflux
Don’t forget the q line. Min reflux occurs at intersection with
equilibrium curve because all three lines should intersect
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XB Xa
XD
Minimum Reflux

Can also be calculated (if feed is liquid at b.p.)

1  xD α (1 − xD ) 
Rmin =  − 
(α − 1)  xF (1 − xF ) 

Or, using definition of slope of line = R/(R+1)

xD − y '
Rmin =
xD − x '

Where x’, y’ is the intersection of line with curve
Optimum Reflux Ratio (From McCabe Smith Ch21)

Increase R

Diameter gets bigger
– Since D = fn(V, L)
– R ↑ ⇒ V & L ↑ ⇒ D ↑ ∴ Capital Cost ↑

No. of Plates gets smaller
– Height ↓ ∴Capital Cost ↓

Heat exchangers get bigger
– Boiling/Condensing ↑∴ Capital & Running Cost ↑
Optimum Reflux Ratio

Total Cost
Annual Cost

Min Reflux Ratio

Optimum Reflux Ratio Operating Cost

Captial/Fixed
Cost
1.0 1.2 1.4 1.6 1.8 2.0
Reflux Ratio
Reflux and Cost
A trade off between operating cost and capital cost is
needed.
Increase R ⇒ Less stages, less capital cost BUT also ⇒
More boiling and condensing
Decrease R ⇒ More stages, More capital cost BUT also ⇒
Less boiling and condensing
Capital and operating costs combine to give a total cost.
This is minimised with the following
Rule of thumb - R = 1.1 to 1.5 times Rmin
R determines the slope
Change in slope means less or more stages. As R increases
the slope approaches 1. More MVC returned to the column.
Less material is removed
as distillate. Separation
improves, fewer trays
needed
As R is decreased, the
slope decreases towards
the equilibrium line.
A ‘pinch’ between
operating and equilibrium
lines becomes more
pronounced and more and
more trays are required
Activity – Reflux Ratio

Think, Pair, Share the following:

Calculate R for the Acetic Acid/Acetic Anhydride

system from last week.
Reflux Control

Source: http://www.controlguru.com/wp/p68.html
McCabe Thiele Method
Developed in 1925
Suitable for binary mixtures in continuous columns
Can be used as a preliminary study for multi component
Combination of VLE data and operating lines
Assumes:
Constant molal overflow
No heat loss from column
Not suitable if:
Relative volatility is < 1.3 or > 5
Reflux ratio < 1.1 Rmin
More than 25 theoretical stages needed
Specifications required
The following information is needed
F Total feed rate
zF Mol fraction of MVC in the feed
P Column operating pressure
xD Mol fraction of MVC in the distillate
xB Mol fraction of MVC in the bottoms
R/Rmin Ratio of reflux to minimum reflux
Results provided
McCabe Thiele provides the following results
D Overall distillate flowrate
B Overall bottoms flowrate
Nmin Minimum number of equilibrium stages
Rmin Minimum reflux ratio (Lmin/D)
R Reflux ratio (L/D)
VB Boilup ratio (V/B)
N Number of equilibrium stages
xn, yn Vapour and liquid compositions at each of the stages
Design Procedure
Start with VLE data and draw an x-y diagram
Determine the three operating lines and draw them on the x-y
diagram
Using the rectifying operating line and the equilibrium curve
draw steps from the distillate composition to the feed point
Count the number of steps. Each one equals an equilbrium
or theoretical stage
Using the stripping operating line and the equilibrium curve
draw steps from the bottoms composition to the feed point
Add the number of steps to the previous to give the total
number of equilibrium stages
Convert this to a number of plates by dividing by the plate
efficiency.
 Design Illustrated
slope=R/(R+1) 1. Obtain VLE curve
1.0
slope= (VB +1) /VB
2. Pick distillate composition,
0.9 XD, and Reflux ratio, R, and draw
0.8
operating line for rectification
6
5 3. Pick bottoms composition, XB,
0.7
4 and Boilup ratio, VB, and draw
0.6
operating line for stripping
3
Ya

0.5
4. Start stepping off from the
0.4 distillate end until the
XD/(R+1) 2
0.3
intersection of the two operating
lines is passed.
0.2
5. Continue stepping but use the
0.1 1 stripping operating line
0.0
6. Count the number of stages
0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0

XB Xa 7. Subtract one for the reboiler to

XD
give the number of theoretical
trays (or leave as safety factor)
Activity – Count no. of stages

Think, Pair, Share the following:

Determine the number of equilibrium stages needed to effect

the specified separation for the Acetic Acid/Acetic
Anhydride system
Is it OK to use equilib curve and op line?
I know the no. of equilibrium stages
The hard work is done at this point. The no. of equilibrium
stages must be converted to a number of actual real plates.
Typical values for tray efficiency are 0.5 to 0.75, I.e. they are
0.5 to 0.75 times as effective as an ideal stage.
Divide the number of ideal stages by the efficiency.
Don’t forget the boiler. This counts as one ideal stage.
Delete 1 or leave it in as a safety factor.
Add 10% extra trays.
Trays and Plates
Trays and plates encourage vapour liquid contact so that
falling liquid partially vaporises and rising vapor partially
condenses to create more equilibrium stages.
This involves heat transfer which takes time. The plate
provides an environment in which this can happen.
Trays should aim to minimise pressure drop.
The main designs are….
Bubble cap
Sieve tray
Valve tray
The Bubble Cap Tray
A number of small caps mounted on a riser. The cap is wider
than the riser so the vapour flows up the riser and is then
forced down around it on to the tray. A shallow pool of
liquid is retained on the tray by means of a low weir. The
area of the riser and the annular area between the riser and
cap should be kept equal so the flowrate is not restricted.
Trays suit medium to large sized columns (0.3 to 5m). On
small diameter columns, installation and cleaning is difficult
Bubble cap trays
The Sieve Tray
Sieve tray - a horizontal perforated sheet with a weir on one
side. Same diameter as the column. The vapour passes
through a shallow pool of liquid.
The Valve Tray
Like the sieve tray. A number of perforations but each
perforation is covered by a flap or valve which is only lifted
by the vapour flow. The tray may be modified to contain
risers like the bubble cap tray in which case the valve sits on
top of the riser. Vapour flow depends on the flow rate itself,
these trays can operate over a wide range of flow rates. It is
not necessary to replace the trays if the flow rate is changed.
Valve trays
Problems with Trays
Adverse vapour flow conditions can cause….
Coning - liquid rate too low. Vapour forces liquid away
from slots and passes through as a continuous stream. No
mixing
Dumping - vapour rate too low. Some slots dump liquid and
don’t pass vapour. Vapour accumulates and eventually
passes as a pulse.
Weeping - combination of pulsating vapour flow and
dumping.
Problems with Trays contd…
Flooding - vapour rate too high. This creates hold-up of
liquid on the plate. Creates an increase in column pressure
drop.
Entrainment - high vapour flow carries liquid back up the
column to the previous tray.
Foaming - liquid expands due to passage of vapour.
Although a large vapour liquid interfacial area is created,
foaming can cause severe hold up of liquid on a tray.
The vapour rate must be adjustable to get it right
Tray Efficiency - Murphree
For an ideal tray, the vapour leaving is in equilibrium with
the liquid leaving.
This may not happen in practice.
The Murphree efficiency is defined as:

yn − yn −1
EMv =
ye − yn −1
Where Emv = Murphree efficiency for vapour
yn = actual vapour composition of tray n
yn-1 = actual vapour composition of tray n-1
ye = vapour composition in equilibrium with liquid
on tray n
Packing
Can be used instead of trays
Very useful for small columns where installation of trays is
difficult
Packing typically has a lower pressure drop than trays which
makes it favourable for vacuum columns
Vapour liquid contact may not be as good. The liquid moves
towards the walls and vapour flows more readily in the areas
free of liquid.
Redistributors may be necessary
Quantity of height of packing = no. of stages x HETP
HETP = height equivalent to a theoretical plate
Types of Packing
Pall rings, raschig rings and saddles are easily available

They provide a large interfacial area and minimise short

circuits for flow
They come in different sizes – e.g. small and large pall rings
Packing Support

Install at base of column to hold packing and allow

vapour to pass
HETP
The height of a particular packing that is equivalent to a
theoretical plate does not just depend on its physical shape.
The vapour flow rate up the column also affects this number.
1.5 to 2” sizes of common packings allow the same vapour
velocity as a sieve tray and have a HETP of 0.3 to 0.6 m
(Unit Ops, McCabe Smith, 6th Ed., p699)
What improvements should this man make to his design?
What would you say to him? (He is making Raki)