606 Chapter 10
Refrigeration and Heat Pump Systems
Intercooling is accomplished in this cycle by means of a direct contact heat
exchanger. Relatively low-temperature saturated vapor enters the heat exchanger at
state 9, where it mixes with higher-temperature refrigerant leaving the first compres-
sion stage at state 2. A single mixed stream exits the heat exchanger at an intermedi-
ate temperature at state 3 and is compressed in the second compressor stage to the
condenser pressure at state 4. Less work is required per unit of mass flow for com-
pression from 1 to 2 followed by compression from 3 to 4 than for a single stage of
compression 1–2–a. Since the refrigerant temperature entering the condenser at state
4 is lower than for a single stage of compression in which the refrigerant would enter
the condenser at state a, the external irreversibility associated with heat transfer in
the condenser is also reduced.
A central role is played in the cycle of Fig. 10.10 by a liquid–vapor separator, called
a flash chamber. Refrigerant exiting the condenser at state 5 expands through a valve
and enters the flash chamber at state 6 as a two-phase liquid–vapor mixture with
quality x. In the flash chamber, the liquid and vapor components separate into two
streams. Saturated vapor exiting the flash chamber enters the heat exchanger at state
9, where intercooling is achieved as discussed above. Saturated liquid exiting the flash
chamber at state 7 expands through a second valve into the evaporator. On the basis
of a unit of mass flowing through the condenser, the fraction of the vapor formed in
the flash chamber equals the quality x of the refrigerant at state 6. The fraction of
the liquid formed is then (1 2 x). The fractions of the total flow at various locations
are shown in parentheses on Fig. 10.10.
flash chamber
10.5 Absorption Refrigeration
Absorption refrigeration cycles are the subject of this section. These cycles have some
features in common with the vapor-compression cycles considered previously but
differ in two important respects:
c One is the nature of the compression process. Instead of compressing a vapor
between the evaporator and the condenser, the refrigerant of an absorption system
is absorbed by a secondary substance, called an absorbent, to form a liquid solution.
The liquid solution is then pumped to the higher pressure. Because the average
specific volume of the liquid solution is much less than that of the refrigerant vapor,
significantly less work is required (see the discussion of Eq. 6.51b in Sec. 6.13.2).
Accordingly, absorption refrigeration systems have the advantage of relatively
small work input compared to vapor-compression systems.
c The other main difference between absorption and vapor-compression systems is
that some means must be introduced in absorption systems to retrieve the refriger-
ant vapor from the liquid solution before the refrigerant enters the condenser. This
involves heat transfer from a relatively high-temperature source. Steam or waste heat
that otherwise would be discharged to the surroundings without use is particularly
economical for this purpose. Natural gas or some other fuel can be burned to provide
the heat source, and there have been practical applications of absorption refrigera-
tion using alternative energy sources such as solar and geothermal energy.
The principal components of an absorption refrigeration system are shown sche-
matically in Fig. 10.11. In this case, ammonia is the refrigerant and water is the absor-
bent. Ammonia circulates through the condenser, expansion valve, and evaporator as
in a vapor-compression system. However, the compressor is replaced by the absorber,
pump, generator, and valve shown on the right side of the diagram.
c In the absorber, ammonia vapor coming from the evaporator at state 1 is absorbed
by liquid water. The formation of this liquid solution is exothermic. Since the amount
of ammonia that can be dissolved in water increases as the solution temperature
absorption refrigeration
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