Lecture2 PDF
Lecture2 PDF
Partitioning and coupling methods: -The mesh equations are grouped either by stage or by
type. Initials estimates for some variables are required for starting the calculations. For a
given set of variables the groups of equations are solved in a predetermined order, the other
variables being kept constant. These last variables are updated according to the previous
result by using direct substitution method. This procedure is continued until a convergence is
achieved. Within this category the different approaches can be used.
1. Stage to stage methods: - In this class of methods, the procedure of Lewis and
Matheson, Thiele and Geddes, and the method of Holland are used. The mesh
equations are grouped stage to stage and solved from bottom to top.
2. Partitioned by type of equation: - in this approach temperature and flow rates must
be initialised. The mass balance equations are combined with the equilibrium
equations to form the first set of equations. These equations are linearised by keeping
the constant flow rates and equilibrium constants, and then they are solved component
by component. By using the new values of compositions, the sum and enthalpy
balance equations can be solved either simultaneously or separately in order to obtain
the new temperature & flow rates profiles.
Global and simultaneous procedures: In this class of methods, the mesh equations are linearized and simultaneously solved by
means of Newtons-Raphson Method. A Jacobian matrix containing a large number of partial
derivatives (numerically or analytically) must be generated and the equations are solved with
the initial set of variable.
Mathematical model: Consider the column shown in following figure, involves N plates numbered from top to
bottom, including a condenser (total or partial) numbered 1(one) and a reboiler numbered N.
The liquid (molar flow L ) and vapour (molar flow V ) coming from the stage j from a liquid
vapour equilibrium. On each stage j, a feed stream F and liquid (SL ) and vapour (SV ) side
stream are planned. Heat supplies or losses Q on each plate are taken into account, so nonadiabatic column can be studied.
Q 1 (Q c)
Stage 1
V2
SV2
F2
V1 (D v )
L1
Stage 2: P2T2
SL1 (DL )
Q2
SL2
VJ+1
SVJ-1
FJ-1
QJ-1
VJ
LJ-1
SVJ
FJ
SLJ-1
(J) PJ TJ
QJ
LJ
VJ+1
SVJ+1
FJ+1
QJ+1
SLJ+1
LJ+1
VN-1
SVN-1
FN+1
SLJ
SLN-1
LN-1
QN (QB)
Stage N
LN (B)
(W)
SVj
Fj
Vj
Lj-1
ij
Xi,j-1
Yi j
Ij-1
Qj
Theoretical plate j
Zi j
Vj+1
SLj
Yi, j+1
Jj+1
Lj
26.1
26.2
26.3
This equation is based on the assumption that each plate is a theoretical plate, that is
to say that liquid vapour equilibrium exists on each plate between the two phases
coming from it.
Sum equations(S)
)=0
26.4
26.5
This enthalpy balance is based on the assumption of an ideal heat transfer, i.e. the vapour and
liquid stream coming from each plate have the same temperature. In addition to these
equations, and correlations are required to predict the equilibrium constants and the
enthalpies. These correlations are often complex equations describing relations between
thermodynamic properties and state variable.
Degree of freedom:
In order to define the problem, all the feed flows F feed composition Z
temperatures and pressure are fixed. All the liquid and vapour side stream flows SLj , SVj , as
well as the amounts of heat supplied Q (2 j N 1) and the pressure Pj are also fixed.
In the case of a total condenser V1 =0, the heat QN supplied to the reboiler is fixed and the
reflux ratio, R=L1/SL1, is also fixed when the side stream flow rate is given. In the case of a
partial condenser QN and the heat supplied to the condenser Q1 are fixed. So the unknowns of
the problem are liquid and vapour compositions Xi j , Yi j , the temperature Tj on each plate,
the liquid(L1 to LN) and vapour(V1 to VN) molar flow i.e to.