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THERMODYNAMIC ANALYSIS
3.1 INTRODUCTION
state point 6. At this point the temperature and pressure are If. and PL, respecti\el\.
From state point 6 the secondary stream due to suction effect reaches to the
stagnation state These two streams mix thoroughly in the mixing chamber of the
ejector and travels through the diffuser. At the outlet of the diffuser the refrigerant
is at temperature 14. and pressure P4= PL (State point 4). From state point 4 the
refrigerant flow-, through the condenser. While passing through the condenser the
heat Qc is rejected to the cooling water. After rejecting the heat in the condenser
the refrigerant comes out of the condenser at state point 1.
3.3 AN AI YSIS OF EJECTOR
3.3.1 Ejector
There are basically two methods for analysing the ejector (viz. constant
pressure mixing and constant area mixing). Many investigators Viz. Tlrod et.all
[1945|. f)e Prate and Hoerl [1959], Keenan et al [ 1950). and George Emmanuel
[19761 have reported that the constant pressure mixing yields better result.
Therefore in the present study the theoretical model based on one dimensional
flow and constant pressure mixing is developed.
h. Enthalpy ( k.Ekg )
Fig. 3. 3 (a) p-h Diagram for Power Sub- cycle
h Enthalpy ( k.I'kg )
The elector refrigeration system consists of two sub cycles. namely Power
sub- c\cle and the other the Refrigeration sub- cycle. The p - h diagram tor the
Power c>clc is shown in fig. 3.3(a). The process involved in this cycle are
explained as follows:
Process 12: A part of the liquid refrigerant from the condenser is pumped
as primary fluid to the generator inlet at a pressure P2
Process 2-3: Heat added to the refrigerant at constant pressure in the
generator. The refrigerant is at a dry saturated vapour state at a
pressure and temperature of P2 and IT respectively.
Process 3-6: Expansion of Primary vapour in the primary Convergent-
divergent Nozzle to a pressure Pc .
Process 6-4: Mixing of primary and the secondary vapour in the mixing
chamber and the combined (mixed) vapour is self compressed
to the condenser pressure Pc at the exit of the ejector.
Process 41: Heat is rejected from the refrigerant at constant pressure in the
Condenser. At the exit of the condenser the pressure and the
temperature are Pc and Tc respective!).
The P-h diagram for the refrigeration sub cycle is shown in Fig. 3.3 (b). Th
processes involved in this cycle is as follows:
Process 1 5: The expansion of the secondary flow refrigerant liquid (from
exit of the Condenser ) in the expansion valve to a pressure Pc.
Process 5-6: The refrigerant absorbs heat in the evaporator and at the exit of
the evaporator the pressure and the temperature are Pe and
1 c respectively .
Process 6-4: Compression of the combined (primary and the secondary )
Vapour to a condenser pressure at the exit of the ejector.
Process 4 1 : Heat is rejected from the refrigerant at constant pressure in the
41
I I lie primary mass flow exceeds the secondare mass flow in the
elector
at the entrance
walls
streams
5. The expansion in the primary nozzie and the compression of the
The mass flow rate (m) and the velocity (v) of refrigerant across Ejector
m - A.A' (3.1)
h - V- : = h „ (3.4)
43
C" kR I
From l.qn. (3.4) & (3.5) the Mach Number function is obtained as
Mass How rate per unit area for the primary nozzle in terms of Mach
number can be derived from Eqn. (3.1) as:
At the throat 'f the Mach number is unite. Hence the primary nozzle flow
equation is .
From Lqn. (3.7) & (3.8) the exit area A pa of the primary nozzle is obtained as
The actual enthalpv change at the convergent - divergent nozzle is smaller than the
isentropic enthalp> change. Hence, the nozzle efficiency qn is defined as
Similarly the Mach number of the secondare vapour at the exit of the
prirnan nozzle plane (section 'a' ) is given by
In the mixing section the pressure at section "b" and 'x‘ are assumed to be the
same as IT Also, only for the condition that Pa= Ph= Px the ultimate expansion is
realised in the nozzle ( Lames et.al.\ 1995]). Writing the equation for the mixing
section
m r - m.-mb-mx-AxpxVx (3.13)
Conservation of momentum
M \ ’ | kx (K Wx )\\ | (3.16)
11'the primary v apour and the secondary vapour are not the same, then the mixer
molecular weigh) W x . is calculated as
Vx Up Vp, (3.20)
(since momentum of secondary flow and the momentum at the exit of the ejector
at section (4) are negligible ).
Cl , I I« v: 2 h „ ) = M: (k-I ) 2 (3.22s
i/7 (3.25)
Where.
Substituting the various values of pp. hop. u and h ov the value of 0 becomes.
0 -1 Am. mp); Mm. /mp)(h Top)J■ {[1- Mpa2 (k-1) 21 [ M pa:( k-1) 2 ]
(3.30)
Stagnation Enthalpy Ratio, h h op. is given from equation (3.22) as:
Shock Analysis
Similarlv the ratio of pressure before the shock 1\ and after the shock P} is giv en
bv
P, P = 11- kMc] [1-kMc] (3.33)
4X
1 he subsonic mixed How after the shock in constant area section enters
the diffuser and compressed further until its velocity decreases to zero (assumed at
Ejector Efficiency
done during the lsentropic compression of the secondare vapour from P(ls to PL. to
the w ork done during isentropic expansion of the primary vapour from P(>r to I\
Area ratio
The area ratio is defined as the area of the mixing section A xto the area
of the primary nozzle throat At. This area ratio is more important design parameter
(3.3b)
4b
, j i kp• I) !2 ( kp
A |I\,rU2 (kp- 1) M
■v 1 p j i '
Mm i \ k.
‘ mu i \ . <P P (P, p j:: MpPikp-l ) 21
(3.3")
This equation is often used for optimisation of the mass flow ratio, for the given
The I F( i used in the thermodynamic model is the one which is produced by Madras
Refineries Ltd., me constituents are.
- 56.086
From the above theoretical analysis it is seen that all four refrigerants are
suitable as a w orking fluids in a ejector refrigeration systems. The Ozone Depletion
Potential for certain refrigerants is listed in Table 3.2.
49( b
Chemical
Refrigerant Name Designation ODP
formula
I richlorofluoromethane CCPF R11 1.00
Dichlorodifluoromethane CCEPT R12 1.00
C h 1 or od i fl uor om ethan e CHC1F3 R22 0.05
Dichlorotrifluoroethane CHCFPT R123 0.02
Tetrafluoroethane ; CH2FCF? R134a | 0
Ammonia 1 NFL R717 ! 0
The above data has been taken from reference Eastop ei.al (1995)
From the fable 3.2 it is evident that the Ozone Depleting Potential of
R134a is zero and hence R134a has been chosen as the working fluid for the
experimental analysis.