Part 2 Separation Engineering
Part 2 Separation Engineering
LIQUID
EXTRACTION
EXPECTED OUTCOMES
1. Explain the basic theory & principle of LLE.
2. Demonstrate the LLE under batch &
continuous mode.
3. Calculate number of theoretical stages and
height equivalent to a theoretical stage using
theory as well as graphical methods.
4. Discuss industrial LLE equipment.
Single-stage
Extraction
Single-stage Extraction
O Referring to Fig. 10.12 (Treybal), it is a bit different as
compared to Fig. 23.7 (McCabe).
O But not for the orientation of extract phase (left) & raffinate
phase (right).
O Fig. 10.12 shows the extraction of component C from A by
using solvent B.
The equilibrium data at 20 °C are listed below. [Trans. AIChE, 36, 628
(1940), with permission].
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Solution 2 a):
The horizontal rows give the concentration in equilibrium
solutions. The system is of the type shown in Fig. 10.9a,
except that the tie lines slope downward the B apex. The
rectangular coordinates of Fig. 10.9b will be used, but
only for acid concentrations up to x = 0.30. These plotted in
Fig. 10.15.
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
Multistage Counter-current
Extraction
O If an extraction to give the same final raffinate
concentration x = 0.20.
O It must be done in one stage, the point M would be at the
intersection of tie line R3E3 and line FS of Fig 10.15.
O So, XM= 0.12.
O The solvent required would then be, by EQ. 10.6:
O The liquid feed stream (L) and the solvent stream (V) are
relatively immiscible in each other.
O Solute A is relatively dilute in both stream.
O Outlet feed stream is raffinate, outlet solvent stream is extract.
O Overall material balance for countercurrent extraction EQ.
5: �1
� ′ �1−+ �′( )=� ′ � 1 + � ′ 1−�
�
1
1−� 1−�
�
1
L’ = kg feed B/h
V’ = kg
solvent/h
y = mass fraction A in solvent V
stream x = mass fraction A in feed L
stream
Design Towers for
Extraction (Geankoplis 4th edition)
2) Limiting solvent flows and optimum L’/V’ ratios Fig. (a) & (b):
O The inlet feed flow L2 and its composition x2, are usually set.
O x1 in the raffinate (L1) set by designer, y1 in the raffinate (V1) is
generally fixed by process requirements.
O Hence, the entering flow V1 or V’ is open to choice.
O x1, x2 and y1 are set. When the operating line has a max slope,
touches the equilibrium line at point P, then the solvent flow is at
a minimum at V’min. The y2 is at max of y2,max.
O For absorption and stripping, flow rate is taken as 1.2-1.5 times
V’min.
O If equilibrium line is curved/concave upward, V’min is a tangent to the
equilibrium line.
Design Towers for
Extraction (Geankoplis 4th edition)
Design Towers for
Extraction (Geankoplis 4th edition)
3) Operating-line equation for relatively immiscible liquids:
]
Design Towers for
Extraction (Geankoplis 4th edition)
O For V phase, EQ.
10:
�� = (�1 −
�
(� −
�2)�∗)�
O If operating and equilibrium lines are curve, EQ.
11:
1 � 2 −�
� � � (1−� ln[ (1 − �) 1( �� ) +
� 1 −�
= ) �] 1