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Chapter : Process
File Reference: CHE21003
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
CONTENTS
PAGES
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
LIST OF FIGURES
Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.
Enthalpy Values................................................................................................................. 15
Figure 6.
Figure 7.
Figure 8.
Figure 9.
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Aqua-ammonia systems
Water-lithium bromide systems
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
In Step 1, hot liquid refrigerant is expanded into a low-pressure, low-temperature liquid and vapor in the
evaporator. The expansion of the refrigerant cools the refrigerant due to the heat of vaporization. The cold
refrigerant provides the cooling power.
In Step 2, the cold, low-pressure refrigerant vapor is converted to a liquid in solution while the low-pressure is
maintained. This conversion occurs when the refrigerant is miscible with the solution base (absorbent) and
when there is a high affinity between the refrigerant molecules and the absorbent molecules. Thermal energy
due to the heat of condensation, sensible heats, and heat of dilution is generated in this process. This thermal
energy must be removed with minimal heating of the refrigerant-absorbent mixture.
In Step 3, the refrigerant-absorbent mixture is pressurized.
In Step 4, the refrigerant-absorbent mixture passes through a heat exchanger where the mixture is heated.
In Step 5, the refrigerant-absorbent mixture undergoes distillation and separates the refrigerant from the
absorbent. If the pure absorbent material is nonvolatile, a simple still is adequate. If the pure absorbent
material is volatile, fractional distillation is required. It is critical that the refrigerant that is obtained in this step
be free of absorbent. The refrigerant from this step is a hot, high-pressure vapor. The absorbent obtained in
this step may contain significant amounts of refrigerant.
In Step 6, the hot, high-pressure refrigerant vapor passes into a condenser. The condenser cools the vapor
sufficiently to convert the vapor to a liquid.
The hot absorbent from Step 5 is transferred through the heat exchanger in Step 4 to heat the refrigerantabsorbent mixture, and at the same time, to cool the regenerated absorbent. The regenerated absorbent is then
supplied as the absorbent for Step 2.
Critical characteristics of the refrigerant-absorbent pair are as follows:
The refrigerant and the absorbent should not form a solid over the range of composition and
temperature to which they may be subjected.
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
The absorbent should have a strong affinity for the refrigerant under the conditions in which the
absorption takes place.
The operating pressures should be moderate. The operating pressures are largely determined by
the refrigerant.
The refrigerant, the absorbent, and the mixture should all be chemically stable. They are subjected
to severe conditions over years of service.
The refrigerant, the absorbent, and the mixture should be non- corrosive. Corrosion inhibitors
should be used as necessary.
The refrigerant's latent heat should be high. High latent heats allows the circulation rate of the
refrigerant and absorbent to be kept to a minimum.
The fluids should have good transport properties (viscosity, surface tension, thermal diffusivity,
and mass diffusivity).
No known refrigerant-absorbent pair has all of the critical characteristics that are listed. Two commonly used
pairs are ammonia-water and water-lithium bromide. In the following section, the operations of these
refrigerant-absorbent pairs are discussed. Critical characteristics are discussed in a later section.
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Point 1 to 2
Hot water leaves the generator. This water is cooled in the heat exchanger by the incoming ammonia-water
(4A). The cold water is then sent to the absorber.
Point 2 to 3
In the absorber, the cold water absorbs low-pressure ammonia that comes from the evaporator. The ammoniawater then enters the strong aqua (SA) tank.
Point 3 to 4
The ammonia-water from the (SA) is pumped to the generator system through the heat exchanger. In the heat
exchanger, the ammonia-water is heated by the water that was produced at point 1.
Point 4 to 5
The hot ammonia-water from the heat exchanger enters the distillation tower and, through the tower, the
generator system. In the tower and generator system, the ammonia is separated from the water. The hot water
then leaves the generator at point 1.
Point 5 to 6
The gaseous ammonia leaves the tower and enters the condenser where the gas is converted to liquid ammonia.
Point 6 to 7
The liquid ammonia is expanded in the evaporator, where the liquid is converted into cold liquid and gaseous
ammonia. The cold liquid vaporizes and cools the evaporator. The cold, gaseous ammonia is then transferred
to the absorber. In the absorber, the cold, gaseous ammonia is absorbed by the water.
Point 8
Upsets in the tower or changes in evaporator operation could cause the concentration of water in the liquid
ammonia to increase. The periodic spillover connection allows the return of accumulated water to the system.
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Point 1 to 2
Hot lithium bromide leaves the generator. This lithium bromide is cooled in the heat exchanger by the
incoming lithium bromide-water. The cold lithium bromide is then sent to the absorber.
Point 2 to 4
In the absorber, cold lithium bromide absorbs the low-pressure water vapor that comes from the evaporator.
Point 4 to 5
The cool, lithium bromide-water is pumped from the absorber to the generator through the heat exchanger. In
the heat exchanger, the lithium bromide-water is heated by the lithium bromide that was produced at point 1.
Point 5 to 1
Hot lithium bromide-water from the heat exchanger enters the generator. In the generator, heat is added to
distill the water. Hot lithium bromide leaves the generator at point 1.
Path 6 to 7
Hot, high-pressure water vapor (6) condenses (7).
Point 7 to 8
The hot water expands in the evaporator. The expansion vaporizes the water, which becomes the evaporator.
The cold, low-pressure water vapor is absorbed by the solution in the absorber .
Engineering Encyclopedia
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Absorption Refrigeration Systems
Absorption refrigeration equipment is classified by how it is fired and whether it has a single-stage or two-stage
generator. Units that use steam or hot fluid heat sources are indirect fired. Units that use a flame heat source
are direct fired. Units that use hot waste gases as a heat source are indirect fired, but are often referred to as
heat-recovery units. Units with two-stage generators are called dual-effect or double-effect units.
Aqua-Ammonia
The ammonia-water pair (aqua-ammonia absorption system) meets most of the ideal requirements for an
absorption refrigeration system. However, the volatility ratio is too low; high operating pressures are required;
and ammonia is an ASHRAE 15-1978 Safety Code Group 2 fluid, restricting its indoor use.
The low volatility ratio means that it is difficult to completely separate the ammonia from the water and
requires a compromise in the refrigeration system. There are two possible solutions. In the first solution, the
refrigerant will have water vapor present as it passes through the condenser and evaporator, which restricts the
refrigerant pathway which can freeze at 0C (32F). In the second solution, the water that serves as an
absorbent will have a significant amount of ammonia already absorbed and will consequently perform as a less
efficient absorber. Because water is present throughout the system, ammonia-water absorption should not be
used for applications near or below 0C (32F).
Engineering Encyclopedia
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Absorption Refrigeration Systems
The high operating pressures increase the cost of the refrigeration equipment and also increase the inherent
dangers associated with the equipment. The condenser pressures are around 2068 kPa (300 psia) and the
evaporator pressures are around 483 kPa (70 psia).
Ammonia is an ASHRAE 15-1978 Safety Code Group 2 fluid because it can cause serious injury to people at
concentrations of 0.5 to 1.0 percent for durations of exposure over one half hour. Therefore, the use of an aquaammonia refrigeration cycle in an enclosed space, especially in a space routinely inhabited, is discouraged.
Direct-fired, air-cooled ammonia-water liquid chillers are available in 3- to 5-ton (10- to 18-kW) capacities.
Lithium Bromide
The water-lithium bromide pair (lithium bromide-absorption system) meets most of the ideal requirements for
an absorption refrigeration system. However, the pair has the following disadvantages:
The fact that water freezes at 0C (32F) means that a lithium bromide-absorption system cannot be used for
applications requiring refrigeration near or below 0C (32F).
The tendency of the water-lithium bromide mixture to form solids means that the equipment must be designed
to allow a partially crystallized solution to flow, especially from the generator, through the heat exchanger and
into the absorber. It may be necessary to provide a mechanism for removing crystals from the solution, redissolving them, and returning the reconstituted solution to the system. Because the crystallization of the
solution occurs most readily when the solution is air-cooled, the absorber should be water cooled.
Small lithium bromide units of 3- to 30-ton (10- to 105-kW) capacity are available as indirect- or direct-fired,
liquid chiller, chiller-heater, or air-conditioning equipment. Indirect-fired liquid chillers are available in
capacities of 50 to 1500 tons (175 to 5275 kW).
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Sizing Calculations
The following material demonstrates sizing calculations for aqua-ammonia and lithium bromide refrigeration
systems. The objective of this module is to provide only a basic understanding of sizing calculations to help
determine the correct absorption refrigeration process to use for a given application.
For absorption refrigeration systems, the following equation determines the refrigerant flow rate:
RE =
where:
QE
(hv hl )
RE
QE
hv
hl
(EQN A)
Aqua-Ammonia
The following material, including the sample calculation, is extracted from the 1989 ASHRAE Fundamentals
Handbook. In many cases, calculations include values with greater precision than that obtainable from charts
included in this module.
For aqua-ammonia absorption refrigeration systems, the following equation provides the solution flow rate per
unit refrigerant rate (see Figure 2):
WFSA (X) WFSG (X 1) = 1
where:
WFSA =
WFSG =
X =
X-1 =
(EQN B)
Mass of solution from the absorber per unit mass of refrigerant flow
Mass of solution from the generator per unit mass of refrigerant
flow
10
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Absorption Refrigeration Systems
Sample Problem
The sample calculation is performed for a large aqua-ammonia absorption refrigeration plant with the following
conditions:
11
Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Source:
ASHRAE 1989 Fundamentals Handbook (IP Edition) , Atlanta, GA, American Society of Heating,
Refrigerating, and Air Conditioning Engineers, Inc., 1989, p. 17.69, figure 33.
From Figure 4 and the given conditions of 507 kPa (73.5 psia) and 41C (105F) at the absorber, the strong
aqua (SA) solution has an ammonia concentration of 49% by mass.
12
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Process
Absorption Refrigeration Systems
A 6% to 8% concentration increase across the absorber allows sufficient flow and adequate liquid wetting of
plain horizontal tubes % up to 25 mm (1 in) in diameter. The difference between the concentration of ammonia
in solution that enters the absorber and the concentration of ammonia in solution that exits the absorber is
referred to as the concentration split. Concentration splits of 6% to 8% ensure reasonable maximum liquid
flows for cost effective exchangers and towers, and a practical minimum temperature of heat source for the
generator. Large splits reduce the flow rate, efficiency, and cost effectiveness of absorbers and exchangers and
raise the required temperature of the heat source.
For comparison purposes, the calculations will be shown for two splits: 6% and 30%.
With a 6% concentration split, there is a 43% ammonia concentration by mass in the absorbent returned from
the generator to the absorber via the heat exchanger.
Using Equation B, the solution flow rates for a 6% split are the following:
0.49X 0.43(X1)
0.06X + 0.43
0.06X
X
X1
=
=
=
=
=
1
1
0.57
9.5 lb SA/lb refrigerant
8.5 lb WA/lb refrigerant
Given the condenser and tower pressure of 1461 kPa (211.9 psia) Figure 4 can be used to determine the
equilibrium to minimal temperature for the 49% ammonia solution that will enter the heat exchanger. Figure 4
can also be used to determine the equilibrium temperature for the 43% ammonia solution that will leave the
generator as absorbent for the 6% split.
With a 30% concentration split, there is a 19% ammonia concentration by mass in the absorbent returned from
the generator to the absorber via the heat exchanger.
13
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Absorption Refrigeration Systems
Using Equation B the solution flow rates for a 30% split are the following:
0.49X-0.19(X-1) = 1
0.30X+0,19 = 1
0.30X = 0.81
X = 2.7 lb SA/lb refrigerant
X-1 = 1.7 lb WA/lb refrigerant
As with the 6% split, Figure 4 can be used to determine the equilibrium temperature of the 19% ammonia
solution that leaves the generator as absorbent for the 30% split.
For the 49% ammonia solution, the equilibrium temperature for the tower and generator is 80.5 C (176.9F).
For the 6% split, the 43% concentration ammonia-water leaves the tower and generator at a temperature of
90.5C (194.9F). For the 30% split, the 19% concentration ammonia-water leaves the tower and generator at a
temperature of 144.4C (291.9F).
14
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Absorption Refrigeration Systems
Enthalpy values for the ammonia-water from Figure 4 are as presented in Figure 5.
6% SPLIT
ENTHALPY
30% SPLIT
kJ/kg
Btu/lb
kJ/kg
Btu/lb
hl of (1)* WA
166.0
71.4
508.4
218.7
hl of (4)*
112.3
48.3
112.3
48.3
hl of (3)* SA
-65.8
-28.3
-65.8
-28.3
*Numbers in parentheses refer to the circled numbers and corresponding point in the
refrigeration system shown in Figure 2.
The enthalpy at point (2) in Figure 2 in the refrigeration system is determined by mass enthalpy flow rate
balance. This calculation is as follows:
For 6% split (43% ammonia-water):
71. 4 Btu/ lb
218.7 Btu/ lb
15
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Absorption Refrigeration Systems
At these concentrations, Figure 4 indicates the following temperatures for solution entering the absorber (Point
2):
For 6% split: 47.8C (118.0F)
For 30% split: 83.1C (181.6F)
For ammonia-water mixtures at 49% SA, feed conditions of 174F, tower pressure of 211.9 psia, and a vapor
product at 99.95% ammonia, the internal reflux rate is .167 lb/lb refrigerant (1.15 times the minimum reflux).
These values, while specific for the conditions stated, should be adequate for checking a proposal since the
vapor product should always be about the same. For exact calculations, the tower should be calculated through
use of computer programs such as "Process."
Use Figure 4 to calculate the refrigerant flow rate and condenser heat level as follows:
Tower Top
(Point 5)
(Figure 2)
Condenser Outlet
(Point 6)
saturated liquid at 100F and 210 psia
(Figure 2)
read hl = 60 Btu/lb
Evaporator Outlet
(Point 7)
saturated vapor at 41.1F and 75 psia
(Figure 2)
read hv = 548 Btu/lb
H across evaporator = 548 60 = 488 Btu/lb
Refrigerant flow rate (assuming 3% for heat gain through insulation):
12000 Btu/ hr
Ton
lb
= 12664 lb/ hr
488 Btu
16
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Absorption Refrigeration Systems
Heat Out
(Point 6)
Ql
(Condenser)
Qc
(Reflux)
Qr
(Point 1)
QWA
12,664 x 60 =
8,282,294
12,990,643
Heat In
(Feed)
Qf
11,339,131
Absorber Load:
Heat In
6% Split (Btu/hr)
(Point 7)
(Point 2)
9,029,027
Heat Out
(Point 3)
967,656
9,996,683
17
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Absorption Refrigeration Systems
Heat Balance:
6% Split (Btu/hr)
Heat In
Evaporator
10,157,200
11,339,131
16,337,232
17,519,163
Condenser
6,445,976
6,445,976
Reflux Coil
1,076,478
1,076,478
Absorber
8,814,967
9,996,683
16,337,421
17,519,137
Generator
Heat Out
Lithium Bromide
The following material, including the sample calculation, is extracted from the 1989 ASHRAE Fundamentals
Handbook. In many cases, greater precision is obtained through use of calculations than through use of the
charts in this module.
18
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Process
Absorption Refrigeration Systems
For lithium bromide-absorption refrigeration systems, the following equation provides the solution flow rate per
unit refrigerant rate:
WFSA =
WFSG =
X =
Mass of solution from the absorber per unit mass of refrigerant flow
X-1 =
Mass of solution from the generator per unit mass of refrigerant flow
(EQN C)
The sample calculation is performed for a large lithium bromide-absorption refrigeration plant with the
following conditions (single-digit numbers in parentheses refer to circled numbers in Figure 3):
19
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Absorption Refrigeration Systems
For the given values for WFSA and WFSG, X can be calculated using Eqn. C as follows:
(1 0.595)X (1 0. 646)(X 1) = 1
0.405X (0. 354)(X 1) = 1
0.051X + 0.354 = 1
0.051X = 0.646
X = 12.67 lb solution from
absorber/ lb refrigerant
To calculate the amount of coolant flow required to provide the 500 tons of refrigeration, the enthalpy change
of the coolant as it passes through the evaporator is needed. The refrigerant enters the evaporator as a liquid at
110F and leaves the evaporator as a gas at 41.1F.
Enthalpy Evaporator Vapor (8) =
Enthalpy of Liquid From Condenser (7) =
1,079.80 Btu/lb
-77.94
Difference H =
1,001.86 Btu/lb
Use standard steam tables for saturated vapor at 41.1F
Refrigerant Flow (including 2.5% spillover) =
1.025 x
1,296.14
-102.30 lb/min refrigerant
1,193.84 lb/min conc. solution
20
Engineering Encyclopedia
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Absorption Refrigeration Systems
71.70 Btu/lb
47.20 Btu/lb
79.00 Btu/lb
107.00 Btu/lb
1,150.30 Btu/lb
21
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Absorption Refrigeration Systems
Source:
ASHRAE 1989 Fundamentals Handbook (IP Edition) , Atlanta, GA, American Society of Heating,
Refrigerating, and Air Conditioning Engineers, Inc., 1989, p. 17.71, Figure 34.
22
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Absorption Refrigeration Systems
Btu/lb
1,079.8
77.94
9.15
71.7
47.2
79.0
107.0
1,150.3
Calculation
Heat In
Solution
(Btu/min)
(Point 2)
85,598.3
(Point 8)
107,769.3
(Point 9)
22.8
193,390.4
Heat Out
(Point 4)
61,177.8
132,212.6
23
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Absorption Refrigeration Systems
Generator:
HeatOut
Calculation
Solution
(Btu/min)
(Point 1)
127,741
(Point 6)
117,676
245,417
Heat In
(Point 5)
1,296.14 x 79
102,395
143,022
Condenser:
Heat In
Calculation
(Point 6)
Solution
(Btu/min)
102.3 x 1,150.3
117,676
102.3 x 77.94
7,973
109,703
Heat Out
(Point 7)
Evaporator:
500 tons x
12,000 Btu/ hr
hr = 100,000 Btu min
x
ton
60 min
Btu/min
Evaporator Load
100,000
Generator Load
143,022
243,022
Heat Out
Absorber Load
132,213
Condenser Load
109,703
241,916
24
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Absorption Refrigeration Systems
The two totals should be the same. However, there are small differences in reading enthalpy values. The
overall balance is within .46% and is considered complete. The coefficient of performance (COP) is calculated
as follows:
COP =
Evaporator Load
100, 000
=
= .699
Generator Load
143, 022
Double Effect
6.7C (44F)
6.7C (44F)
5.5C (10F)
5.5C (10F)
29.4C (85F)
62-83 kPa
(9-12 psig)
90 mm2 k/w
(.0005 hr ft2 F/Btu)
.065 L/s per kw
(3.6 gpm/ton)
29.4C (85F)
296-896 kPa
(43-130 psig)
90 mm2 k/w
(.0005 hr ft2 F/Btu)
.054 L/s per kw
(3.6 gpm/ton)
9C (16F)
1.5 kw/kw
(18.5 lb/hr per ton)
8C (15F)
.43 g/s per kw
(12 lb/hr per ton)
Source: ASHRAE 1989 Fundamentals Handbook (IP Edition), Atlanta, GA, American Society of Heating, Refrigerating,
and Air Conditioning Engineers, Inc., 1989, p. 13.7, Table 1 & 2.
25
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Absorption Refrigeration Systems
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
t'
h
10
20
30
40
45
50
55
60
65
70
80.0
48.0
100.0
68.0
120.0
87.9
140.0
107.9
160.0
127.9
180.0
147.9
200.0
168.0
220.0
188.1
*240.0
*208.3
*260.0
*228.6
*280.0
*249.1
*300.0
*269.6
*320.0
*290.3
*340.0
*311.1
*360.0
*332.2
78.2
39.2
98.1
56.6
117.9
73.6
137.8
91.0
157.7
108.2
177.5
125.4
197.4
143.4
217.2
160.7
*237.1
*178.4
*256.9
*195.7
*276.8
*213.8
*396.7
*231.6
*316.5
*249.7
*336.4
*267.9
*356.2
*286.1
75.6
31.8
95.3
47.0
114.9
61.7
134.6
77.0
154.3
92.0
173.9
107.9
193.6
123.3
213.3
138.2
232.9
154.0
*252.6
*169.1
*272.3
*185.1
*291.9
*200.7
*311.6
*216.3
*331.3
*232.1
*350.9
*248.0
70.5
25.6
89.9
38.7
109.2
51.7
128.5
65.1
147.9
78.2
167.2
91.9
186.5
105.3
205.8
119.0
225.2
132.6
*244.5
*146.2
*263.8
*159.7
*283.1
*173.5
*302.5
*187.2
*321.8
*201.0
*341.1
*214.9
60.9
21.6
79.6
33.2
98.3
44.7
117.1
56.5
135.8
68.1
154.5
80.4
173.3
92.1
192.0
104.1
210.7
116.0
229.4
128.1
*248.2
*140.0
*266.9
*152.1
*285.6
*164.2
*304.4
*176.1
*323.1
*188.2
53.5
21.2
71.8
32.1
90.1
43.0
108.5
54.1
126.8
65.1
145.1
76.6
163.5
87.4
181.8
99.0
200.2
110.3
218.5
121.6
*236.8
*132.8
*255.2
*144.1
*273.5
*155.3
*291.9
*166.6
*310.2
*178.0
42.1
23.0
60.0
33.2
77.9
43.6
95.8
54.1
113.8
64.7
131.7
75.3
149.6
85.9
167.5
96.5
185.4
107.1
203.3
117.6
221.2
128.1
*239.2
*138.9
*257.1
*149.5
*275.0
*160.1
*292.9
*170.6
28.6
28.7
46.1
38.2
63.6
48.0
81.2
57.9
98.7
67.9
116.2
77.7
133.7
87.8
151.3
97.8
168.8
107.7
186.3
117.6
203.9
127.5
221.4
137.3
*238.9
*147.1
*256.4
*157.0
*274.0
*166.8
13.8
38.9
30.9
47.8
48.1
56.9
65.2
66.1
82.3
75.4
99.5
84.6
116.6
94.1
133.7
103.3
150.9
112.5
168.0
121.6
185.1
130.6
202.3
139.8
219.4
148.8
*236.5
*158.0
*253.7
*167.0
#-0.2
#52.7
#16.2
#61.1
32.7
69.4
49.1
78.0
65.6
86.6
82.0
95.1
98.5
104.0
114.9
112.5
131.4
121.1
147.9
129.5
164.3
137.9
180.8
146.5
197.2
154.9
213.7
163.5
230.1
171.9
#-11.6
#67.1
#3.8
#75.1
#19.1
#83.0
#34.4
#91.1
#49.7
#99.2
#65.1
#107.2
#80.4
#115.6
95.7
123.6
111.0
131.6
126.4
139.5
141.7
147.6
157.0
155.5
172.4
163.4
187.7
171.0
203.0
178.3
*Extensions of data above 235F are well above the original data and should be used with care.
Source: ASHRAE 1989 Fundamentals Handbook (IP Edition) , Atlanta, GA, American Society of Heating, Refrigerating, and
Air Conditioning Engineers, Inc., 1989, p. 17.70.
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Engineering Encyclopedia
Process
Absorption Refrigeration Systems
Work Aid 1:
1.
Decide if the refrigeration system must provide cooling to a temperature at or below the freezing point of
water (0C or 32F). Do not use an ammonia-water or lithium bromide-water system.
2.
3.
If Step 1 or Step 2 does not force a choice, select the system with the best economy. Obtain the
investment and utility requirements from the vendor. Use utility costs specific for the location, and
calculate the operating cost for each proposal. Check the vendor's utility requirements using the methods
given in the sample problems. Choose the most economical system.
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Engineering Encyclopedia
Process
Absorption Refrigeration Systems
GLOSSARY
absorbent
absorption refrigeration
affinity
aqua-ammonia system
COP
direct-fired
double-effect
(dual-effect)
heat-recovery
indirect-fired
Refrigeration units that use steam or hot fluid heat as their heat source.
miscible
refrigerant
spillover
Refrigeration units that are indirect-fired and use hot waste gases.
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Engineering Encyclopedia
Process
Absorption Refrigeration Systems
ADDENDUM
ADDENDUM A: EQUATIONS USED IN ChE 210.03
RE =
where:
QE
(hv hl )
RE
QE
hv
hl
(EQN A)
WFSA =
WFSG =
X =
Mass of solution from the absorber per unit mass of refrigerant flow
X-1 =
Mass of solution from the generator per unit mass of refrigerant flow
(EQN B)
(EQN C)
WFSA =
WFSG =
X =
X-1 =
Mass of solution from the absorber per unit mass of refrigerant flow
Mass of solution from the generator per unit mass of refrigerant flow
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Engineering Encyclopedia
Process
Absorption Refrigeration Systems
hv
hl
QE
RE
WFSA
WFSG
Mass of solution from the absorber per unit mass of refrigerant flow
X1
Mass of solution from the generator per unit mass of refrigerant flow
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