10.5 Absorption Refrigeration 469
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 compression stage at state 2. A
single mixed stream exits the heat exchanger at an intermediate 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 compression 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 en-
tering 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. 10.8 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 exit-
ing 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 sec-
ond 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 x). The fractions of the total flow
at various locations are shown in parentheses on Fig. 10.8.
10.5 Absorption Refrigeration
Absorption refrigeration cycles are the subject of this section. These cycles have some fea-
tures in common with the vapor-compression cycles considered previously but differ in two
important respects:
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. 6.53b in Sec. 6.9). Accordingly, absorption
refrigeration systems have the advantage of relatively small work input compared
to vapor-compression systems.
The other main difference between absorption and vapor-compression systems is that
some means must be introduced in absorption systems to retrieve the refrigerant 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 refrigeration using alternative
energy sources such as solar and geothermal energy.
The principal components of an absorption refrigeration system are shown schematically
in Fig. 10.9. In this case, ammonia is the refrigerant and water is the absorbent. 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.
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
flash chamber
absorption refrigeration
absorber