Lecture2 PDF
Lecture2 PDF
Lecture2 PDF
the first effect and pressure in the first effect is highest and pressure in last effect is minimum, so
transfer of feed from one effect to another can be done without pump.
Vapor
Vapor
Vapor
P1,T1
F
V
P0,T0
Liquid
Condensate
Liquid
Condensate
Liq. Concentrate
Condensate
2) BACKWARD FEED ARRANGEMENT: In this arrangement feed is introduced in last effect and
steam is introduced in first effect. For transfer of feed, it requires pump since the flow is from low
pressure to higher pressure. Concentrated liquid is obtained in first effect.
Vapor
Vapor
Vapor
P1,T1
F
V
P0,T0
Condensate
Liquid
Condensate
Liquid
Condensate
Condensate
Vapor
Vapor
Vapor
P1,T1
P0,T0
Liquid
Liquid
Condensate
Condensate
Liq. Concentrate
Condensate
V1 = C1/A* N0.75
The estimated cost of a single effect (C1) can be obtained from a number of sources once the heat transfer
surfaces requirements are known.
Operating cost :
Operating costs can be divided in to steam cost and all operating costs (labour, cooling water,power and
maintenance) such that
V1 = h*W*C2/S + V0
H = operating time (hr/yr)
W = evaporation rate (Kg/hr)
C2 = cost of steam (Rs/Kg)
S = steam economy
V0 = all operating cost other than the cost of steam (Rs/Yr)
Steam economy can be expressed as:
S = S1+S 1S2+S 1S22+..+S 1S2N-1
S = S1 (1-S2N)/ (1-S2)
Thus V2 becomes
V2 = (1-S2)h*W*C2/S1 (1-S2N) + V0
Total cost
VT = V1 + V2
VT = = C1/A* N0.75 + (1-S2)h*W*C2/S1(1-S2N) + V0
For minimum cost VT/N = 0
0 = C1/N{(N+1)0.75 (N0.75)} + (1-S2)h*W*C2/S1{[1/(1-S2N+1)]-[1/(1-S2N)]}
Ahwc2/C1 = {[(N+1)0.75(N0.75)] * S1(1-S2N)(1-S2N+1)}/(1-S2)2 *S2N
variables for a given end product concentration . To quantise the changes in steam economy , a functional
relationship correlating it with variables should be developed. For this, it is necessary to identify all the
variables which affect the steam economy of a multiple effect evaporator.
Variables of a multiple effect evaporator :
In a evaporator , the variables can be classified as geometrical-operating, and self balancing variables. As
regards the geometrical variable , it is the area of heat transfer surface in each effect of an evaporator .
Hence, N-effect evaporator will have N number of geometrical variables.
From industrial practices .we know that there are some operating variables which plant engineer can
change them independently to annual any imbalance in the operation of an evaporator . They include:
feed temperature, feed concentration ,feed flow rate,and steam temperature (pressure), saturation
temperature (pressure) in the last effect. Feed arrangement (forward/backward/mixed) is also one of the
operating variables. Thus , total number of operating variables is six.
As regards the vapour and liquid streams from each effect of a multiple effect evaporator, they cannot be
changed independently by a plant engineer. Therefore, they are self balancing streams. The variables
associated with these streams are: flow rate, temperature and concentration of liquid streams ; and
saturation temperature(pressure) of each effect. However, temperature of vapour stream equals to the
temperature of liquid stream. In this way , for N-effect effect evaporator the number of self balancing
variables becomes 5N. It is important to point out here that the saturation temperature(pressure) of the
last effect, has already been taken in to account as an operating variable . Therefore, it cannot be
considered as a self- balancing variable. Flow rate of steam to the first effect is the another self-balancing
variable whose value is usually not altered. Thus the total number of net self balancing variables for Neffect evaporator, becomes 5N [=5N-1+1].
The summation of geometrical, operating and self -balancing variables gives the total number of variables
in an evaporator. They are equal to 6N+6[=N+6+5N].
Mathematical model:
A mathematical model of a multiple effect evaporator is a relationship amongst the geometrical, operating
and self -balancing variables. This can be obtained from the equations of material balance, energy
balance, heat transfer rate, and boiling point rise.
For the simplicity of the mathematical model, following assumptions have been made in this analysis:
1.
2.
3.
4.
5.
6.
The vapours entering in to steam chest of respective effects are at their saturation temperature.
There is no sub cooling of the condensate from different steam chests.
Condensation of vapour in steam chest occurs at constant pressure.
There is no carry- over of liquid droplets with vapors leaving the respective effects.
There is no heat dissipation to surroundings.
Heat transfer surface does not undergo fouling.
Design of multiple effect evaporator without boiling point elevation for forward feed :
Equations are developed for the case where boiling point elevations are negligible ,also the effect of
composition on liquid enthalpy is neglected. The equations so obtained are generalized for the case where
boiling point elevations cannot be neglected. For definiteness , forward feeds are employed.
Specifications: F , XF,TF,To,Po,P3(ort3),X3(orl3),U1,U2,U3,equal areas, forward feed, negligible boiling
point elevations.
To find : V0, T1,L1,T2,L2 and A
Actually ,four additional dependent variables exist; namely: V1,V2,X1,X2
V1=F-L1(vapour)
V2=L1-L2 (vapour)
V3=L2-L3(vapour)
P31,T11
P3,T2
P3,T3
P0,T0
P0,T0
P1,T1
P2,T2
TF
V0
L1,T1
L2,T2
V0 (P0,T0)
F-L1 (P1,T1)
L3,T3
L1-L2 (P2,T2)
22.1
Rate equation:
U1A(T0-T1)=V0
Effect -2:
22.2
Enthalpy balance:
L1(h1-h2)+(F-L1)=(L1-L2)2
22.3
Rate equation:
U2A(T1-T2)=(F-L1)1
22.4
Effect -3 :
Enthalpy balance:
L2(h2-h3)+(L1-L2)2=(L2-L3)3
22.5
Rate equation:
U3A(T2-T3) = (L1-L2)2
The above equation describing the triple effect evaporator system constitute a set of nonlinear algebraic
equations that may be solved in variety of way, one of which is Newton raphson method which we will
learn in next lecture.
Design of multiple effect evaporator with boiling point rise for forward feed:
Most solutions that are concentrated in evaporators are mixtures of water and non-volatile salt. The
boiling temperature of the solution some times depend on the salt concentration. The difference between
the temperature(T) of boiling solution and the temperature of boiling water (pure) at the same pressure is
known as boiling point rise(BPR).thus
T = TW + BPR
BPR is a function of the solute concentration. A graph called the Dhuring chart is commomnly used to
determine BPR.
Calculation procedure:
Specifications:
F,XF,TF,thick liquid composition(XP),P,saturated steam pressure(P0),heat capacity(CP), overall heat
transfer coefficient(U).
To find: Heat transfer area(A)
Step-1:
Corresponding to evaporator temperature find out the boiling point of pure water,TW.
Step-2:
From the figures/empirical correlation determine the solution temperature/BPR at TW,XP. This
temperature is also the temperature of the superheated water vapour leaving the evaporator.
Step-3:
A total mass balance and a component material balance are used to calculate the flow rates.
F=V+L
XF F = LXP
Step-4:
Calculate /determine the enthalpies of three process streams
1) Enthalpy of water vapour from the superheated steam tables by solution temperature and pressure
of the evaporator.
2) The enthalpy of the solution can be calculated from there heat capacities .
H = CP(T-TR)
It can also be calculated by the plots or empirical correlations.
3) Latent heat of vaporization taken from steam table at corresponding steam pressure.
Step-5:
Now , write the enthalpy balance
F(hf-hp) + V0 0 = (F-L)(HV hp)
Or, V0 = [ (F-L)(HV hp) F(hf-hp)]/0
Step-6:
From the rate equation
V0 0 = UA(T0 1)
A = V00/U(T0-1)
Effect -1:
F[h(Tf,Xf)-h(1,X1)]+ V0 0 -(F-L1)[H(1) h(1,X1)]=0
U1A1 (T0 1) - V0 0 =0
XF F L1 X1 = 0
Effect -2:
L1[h(1,X1)-h(2)]+ (F-L1)[H(1)h(T1)]- (L1-L2)[H(2)-h(2)]=0
U2 A2 (T1 2)- (F-L1)[H(1)-h(T1)] = 0
L1 X1 L2 X2 = 0
Effect -3:
L2[h(2,X2)-h(3, X3)] + (L1-L2)[H(2) h(T2)] (L2-L3)[H(3)-h (3, X3)]= 0
U3 A3 (T2 3)-(L1-L2)[H-h]=0
L2 X2 L3 X3 = 0