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Exergy. http://dx.doi.org/10.1016/B978-0-08-097089-9.00014-0
2013 Ibrahim Dincer and Marc A. Rosen. Published by Elsevier Ltd. All rights reserved 303
304 Exergy
efficiency of energy production is increased in some cases The trend in most published research on such systems
from current levels that vary from 35% to 55% in conven- is that part of the power or heating or cooling produced via
tional power plants, to over 80% in the cogeneration trigeneration systems are used further to produce an extra
systems. Many researchers (Ghafghazi et al., 2010; Kil- product such as hydrogen gas, liquefied hydrogen, or dried
kis, 2011; Ratlamwala et al., 2012ac) showed that tri- products. Investigations by several researchers on multi-
generation systems and multigeneration systems greatly generation systems demonstrate further improvements in
enhance the overall efficiency of the system. Ratlamwala system efficiency when compared to trigeneration systems.
(2012a) noted that generating multiple outputs from one
source not only increases system efficiency, but also can
enhance a systems cost-effectiveness.
14.4 INTEGRATED MULTIGENERATION
This chapter describes how different systems can be SYSTEMS
integrated to produce several outputs using single energy Multigeneration is usually achieved by combining several
resource. Two case studies illustrate how the overall effi- individual processes, but using a single energy input. In-
ciency of a system can be improved if more than one output tegrated multigeneration often refers to systems that
is attained from the single system or several systems produce multiple inputs with multiple systems or multiple
combined. inputs. When producing cooling and heating using multi-
generation systems, absorption cooling and heating
systems are preferred as such systems can utilize waste heat
14.2 TRIGENERATION from thermal power plants to produce cooling and heating
The concept of trigeneration became of interest as concerns simultaneously. Furthermore, multigeneration systems
grew over fossil-fuel prices and environmental concerns integrated with an electrolyzer can produce hydrogen or can
such as global warming. Trigeneration systems are often be integrated with drying processes.
enhanced forms of cogeneration systems in which the tri-
generation systems produce both heating and cooling 14.5 CASE STUDY: ENERGY AND EXERGY
using thermal energy, whereas a cogeneration system
ANALYSES OF A TRIGENERATION SYSTEM
produces either heating or cooling.
At present, many countries around the world are modi- In this case study, an integrated system for trigeneration
fying their power plants running on fossil fuels so that waste of cooling, electric power, and liquefied hydrogen is exam-
heat from these power plants is utilized to produce heating ined. The system utilizes a combination of a quadruple effect
and cooling. absorption system (QEAS), a Linde-Hampson (LH) gas
The benefit of a trigeneration system is a reduction in liquefaction cycle, and a binary power plant to yield three
not only fuel use, but also operating cost of a power plant. outputs. The case study draws on prior energy and exergy
In countries where carbon taxes have been introduced, tri- analyses (Ratlamwala et al., 2012b).
generation systems can help reduce the level of the carbon
tax by recovering waste heat and converting it to additional
products. Apart from cost savings, trigeneration systems can 14.5.1 System Description
significantly reduce environmental impact because, as with
The trigeneration system considered is shown in Figure 14.1.
trigeneration systems, waste heat is used to produce cooling
Geothermal heat passes through the very high temperature
and heating which otherwise would be produced by either
generator (VHTG) before reaching the binary isobutane
burning fossil fuel or consuming electricity. The ability
power plant, as shown in Figure 14.2.
of trigeneration systems to produce three products from
In the VHTG, a strong solution entering at state 36 is
a single input generally enhances the efficiency of the system
heated and exits as a concentrated ammonia-water vapor at
greatly, indicating better utilization of fuel or other energy
state 37 and as a weak solution at state 38. The stream
resources.
exiting the VHTG at state 38 enters the very high temper-
ature heat exchanger (VHHX) and transfers heat to the
stream from the absorber at state 35. After transferring heat
14.3 MULTIGENERATION
in the VHHX, the stream at state 40 mixes with the stream
The idea of multigeneration is relatively new, and is mainly from the high-temperature generator (HTG) at state 30, and
the subject of research. Few full-scale power plants have exits at state 41. The process of releasing heat to the strong
been commissioned that utilize multigeneration. Multi- solution from the weak solution occurs in the heat ex-
generation systems are expanded and enhanced versions of changers before the weak solution enters the expansion
trigeneration systems. In multigeneration systems, more than valve at state 15. The pressure of the weak solution at state
three outputs are obtained using a single energy source. 15 is then reduced by throttling in the expansion valve. The
Chapter | 14 Exergy Analysis of Integrated Trigeneration and Multigeneration Systems 305
low pressure weak solution exits the expansion valve at at state 31 and a weak solution exiting at state 30. Then the
state 16 and enters the absorber. The concentrated ammonia- concentrated ammonia-water vapors at states 28 and 31 mix
water vapor at state 37 then enters the HTG, where heat is and enter the medium-temperature heat generator (MTG)
transferred from the stream at state 37 to that at state 28. The at state 39. The process continues until the concentrated
transferred heat from the concentrated ammonia-water vapor ammonia-water vapor exiting the low-temperature gener-
at state 37 heats the strong solution entering the HTG at state ator (LTG) at state 7 enters the condenser and the other
34, resulting in a concentrated ammonia-water vapor exiting ammonia-water vapor stream exiting the LTG at state 6 is
input to the condenser heat exchanger, where the concen- l The heat needed to operate the isobutane cycle is provided
trated ammonia-water vapor at state 6 rejects heat and by geothermal water at a temperature 20 C below that of
passes to the condenser at state 8. In the condenser, con- the geothermal source.
centrated ammonia-water vapor at states 7 and 8 reject heat l The pressures at the inlet and exit of the stage 1 turbine
to the environment and are conveyed to the expansion valve, are 3600 and 1000 kPa, respectively.
where the pressure decreases and exiting concentrated l The temperature at the inlet of the stage 1 turbine is
ammonia-water vapor at state 10 enters the evaporator. There, 15 C lower than the geothermal temperature at the inlet
the concentrated ammonia-water vapor gains heat from of the binary power plant heat exchanger.
the hydrogen and the return air from the building envelop, l The condenser pressure of the binary multistage power
before exiting at a higher temperature at state 11. That plant is 400 kPa.
ammonia-water mixture and the weak solution at state 16 l Ninety percent of the electricity produced by the binary
enter the absorber and reject heat and enter the pump as multistage plant is supplied to the LH cycle for com-
a strong solution in liquid form at state 1. pressing hydrogen gas and the remaining 10% is supplied
The geothermal water leaving the VHTG is supplied to the building.
to the binary isobutane cycle to produce power as seen in l The concentrations of the ammonia-water strong solu-
Figure 14.3. The isobutane is heated and vaporized using tion, x [36], and of the ammonia-water weak solu-
the geothermal water from the HTG. This vaporized isobu- tion, x [38], are 0.6 and 0.4, respectively.
tane flows through the turbine generating power, and then l The turbine, compressor, and pump isentropic efficien-
is condensed, pumped, and returned to the heat exchanger. cies are 80%, 70%, and 65%, respectively.
The part of power produced by the binary cycle is utilized
The heat input rate to the VHTG of the absorption
to compress hydrogen gas from state 1 to state 2 in an LH
system is provided using the geothermal water source as
cycle, as shown in Figure 14.4. The exiting geothermal water
follows:
is injected back into the underground water well.
Q_ VHTG Q_ geo (14.1)
where
14.5.2 Analysis Q_ geo m_ geo hgeosource hgeoHTG exit
Mass and energy balances are written for the components The cooling produced by the QEAS is calculated as:
of the integrated system: the QEAS, the isobutane binary
multistage cycle, and the LH cycle. Several assumptions m_ 10 h10 Q_ eva m_ 11 h11 (14.2)
are made in the analysis: The energetic and exergetic coefficients of performance
l About 90% of cooling produced by the QEAS is used (COPs) are defined as:
to precool the hydrogen from 25 C to 16.4 C in the
Q_ eva
evaporator, at a constant pressure of 101.3 kPa. COPen (14.3a)
_
Qgeo W_ p
l The remaining 10% of the cooling is supplied to the
building. _ eva
Ex
l In the LH cycle, hydrogen is compressed from 101 kPa COPex (14.3b)
_
Exgeo W_ p
to 10 MPa.
The actual net power obtained from the binary iso- 14.5.3 Results and Discussion
butane plant driven by the geothermal energy source is
Varying the mass flow rate of the geothermal water m_ geo
expressed as:
significantly affects the performance of the integrated
W_ netgeo W_ turb W_ Piso W_ Parasitic (14.4) system. An increase in the mass flow rate of geothermal
water increases the energy input to the QEAS. The power
The ideal specific work required to compress hydrogen
and cooling load provided to the building are observed
from P1 101 kPa to P2 10 MPa is given as:
to vary as the mass flow rate of geothermal water and
P2 condenser load change. As seen in Figure 14.5, the power
Wcompideal RT0 In (14.5)
P1 varies from 16 to 32 kW and cooling load varies from
However, the actual specific work input to liquefaction 31.6 to 20.6 kW. The increase in QEAS energy input and
cycle per unit mass of hydrogen is expressible as: decrease in cooling load with increasing m_ geo lower the
energetic and exergetic COPs of the QEAS (see Figure 14.6).
Wcompideal These COPs vary, respectively, from 5.0 to 1.7 and from
Wcompactual (14.6)
hcomp 1.2 to 0.4 as m_ geo increases. The decreases in the COPs
Tgeo = 573 K
PowerHouse [kW]
27 29
23 26
19 23
15 20
1.5 1.75 2 2.25 2.5 2.75 3
mgeo [kg/s]
308 Exergy
COPex
COPen
Tgeo = 573 K
3 0.8
2.5 0.7
2 0.6
1.5 0.5
1 0.4
1.5 1.75 2 2.25 2.5 2.75 3
mgeo [kg/s]
directly result from the higher energy input to the QEAS The ambient temperature also affects the performance
and the lower output from the QEAS in the form of a of the system, and the effect of ambient temperature on the
cooling load. The QEAS performance decrease with in- amount of hydrogen gas precooled and liquefied is shown
creasing m_ geo also affects the rate of hydrogen precooling in Figure 14.10. The amounts of hydrogen gas precooled
by the QEAS and liquefaction by the LH system. Figure 14.7 and liquefied are found to be decreasing with an increase in
shows that, with increasing m_ geo , the amounts of hydrogen ambient temperature, varying from 0.95 to 0.31 kg/s and
gas precooled and liquefied decrease from 0.53 to 0.34 kg/s from 0.2 to 0.05 kg/s, respectively, for condenser loads of
and from 0.09 to 0.06 kg/s, respectively. It is thus observed 150, 175, and 200 kW. This behavior occurs because an
that an increase in m_ geo reduces the performance of the system increase in ambient temperature decreases the natural cooling
in terms of cooling production and hydrogen liquefaction. In of the system from ambient air. As the ambient temperature
case of power production, however, an increase in m_ geo increases, the performances of the QEAS evaporator and
enhances the system power production. the LH system both decline, due mainly to the lower temp-
The geothermal water source temperature Tgeo plays erature difference between the surroundings and the system.
an important role in designing and assessing the system.
That parameter also determines if the system is capable of
producing power or limited to low-grade energy applica-
14.6 CASE STUDY: ENERGY AND EXERGY
tions. Figure 14.8 shows that increasing Tgeo decreases the ANALYSES OF A MULTIGENERATION
energetic and exergetic COPs of the QEAS. For a fixed SYSTEM
m_ geo of 2.0 kg/s, the energetic and exergetic COPs vary An integrated geothermal-based multigeneration system
from 3.7 to 2.9 and from 1.1 to 0.7, respectively, as Tgeo for electric power, hydrogen, hot water, cooling, heating,
increases from 473 to 573 K for condenser loads of 150, and dry-air production is examined in this case study. The
175, and 200 kW. An increase in the temperature of the system considered (see Figure 14.11) consists of a quadruple
geothermal source water results in a higher energy transfer flash power plant (QFPP), an electrolyzer, a QEAS, and an
to the VHTG due to the higher potential of losing heat to air-drying process (cooling with dehumidification). This case
the low-temperature stream entering the VHTG from the study follows earlier energy and exergy analyses (Ratlamwala
VHHX. This increase in energy input to the QEAS results et al., 2012d).
in a lower QEAS output, in terms of cooling load, for a
fixed condenser load. The decrease in cooling load reduces
the COPs of the QEAS. As the performance of the QEAS
14.6.1 System Description
degrades, its capability of precooling hydrogen also de- In the integrated multigeneration system, geothermal water
creases. In addition, an increase in Tgeo also affects the is employed as an energy source. The geothermal water
mass of precooled hydrogen gas and the mass of hydrogen passes through the QFPP, where it produces power and hot
gas liquefied, as can be seen in Figure 14.9. The quantities water. Part of the produced power is supplied to the building
of hydrogen gas precooled and liquefied vary from 0.5 to and the remainder is used by the electrolyzer and the solution
0.41 kg/s and from 0.005 to 0.09 kg/s, respectively. pump of the QEAS. The geothermal water exiting the QFPP
Chapter | 14 Exergy Analysis of Integrated Trigeneration and Multigeneration Systems 309
mH2,liquefied [kg/s]
mH2,liquefied at Qcon = 175 kW
0.5 0.092
mH2,liquefied at Qcon = 200 kW
0.48 0.088
Tgeo = 573 K
0.46 0.084
0.44 0.08
0.42 0.076
0.4 0.072
0.38 0.068
0.36 0.064
0.34 0.06
1.5 1.75 2 2.25 2.5 2.75 3
mgeo [kg/s]
at state 20 enters the QEAS, where it releases heat to state 9). The saturated steam at state 3 then enters the very
an ammonia-water mixture. Part of the cooling and all of high pressure turbine, where it expands from 667 to 400 kPa.
the heating produced by the QEAS is supplied directly to The saturated mixture at state 4 combines with the saturated
the building. The remainder of the cooling produced by the steam at state 10 from the second steam separator. The
QEAS is supplied to the air-drying process. The electric streams at states 4 and 10 combine at state 5, and expand in
power supplied to the electrolyzer is utilized to produce the high-pressure turbine from 400 to 300 kPa. The satu-
hydrogen. Descriptions follow in the next sections for each rated mixture exiting the high-pressure turbine at state 6
of the systems. combines with the saturated steam from the third steam
separator at state 12. The streams at states 12 and 6 combine at
14.6.1.1 QFPP state 13, and expand in the medium-pressure turbine from 300
to 200 kPa. The stream exiting the medium pressure turbine
In the QFPP, a high-temperature geothermal source is used at state 14 combines with the saturated steam from the
to produce power as depicted in Figure. 14.12. The high- fourth steam separator at state 17 and at state 18, and
temperature geothermal at a pressure of 3000 kPa at state 1 is expands in the low-pressure turbine from 200 to 100 kPa. The
throttled to 667 kPa at state 2. The resulting saturated stream leaving the low-pressure turbine at state 19 enters
mixture is then separated into saturated water vapor (which the condenser, where it rejects heat to the cooling water
collects at state 3) and saturated liquid (which collects at flowing through the condenser. The cold geothermal stream
3.4 1
3.3 0.95
3.2 0.9
3.1 0.85
3 0.8
2.9 0.75
2.8 0.7
470 492 514 536 558 580
Tgeo [K]
310 Exergy
mH2,liquefied [kg/s]
mH2,precooled at Qcon = 200 kW
0.468 0.07
0.459 0.06
0.45 0.05
0.441 Tgeo = 573 K 0.04
0.432 mH2,liquefied at Qcon = 150 kW 0.03
0.423 mH2,liquefied at Qcon = 175 kW 0.02
mH2,liquefied at Qcon = 200 kW
0.414 0.01
0.405 0
470 492 514 536 558 580
Tgeo [K]
exiting the condenser at state 21 is reinjected into the QEAS as a driving energy source. Part of the electricity
geothermal well in order to maintain the required water level. produced by the QFPP is supplied to the electrolyzer, and
The water used as the cooling medium in the condenser is a small amount is supplied to the solution pump of the QEAS.
supplied to the building as a hot water stream. The saturated
water exiting the first steam separator at state 8 expands
14.6.1.2 Electrolyzer
through the expansion valve from 667 to 400 kPa, exiting
as a saturated water mixture at state 9. The saturated mixture Part of the electric power produced by the QFPP is supplied
at state 9 enters the second steam separator, where saturated to the electrolyzer (see Figure 14.13), where water is split
steam is collected at state 10 and saturated water is collected into hydrogen and oxygen.
at state 7. The latter expands through the expansion valve
from 400 to 300 kPa. The saturated mixture at state 11 then
14.6.1.3 QEAS
enters the third steam separator, where saturated steam is
extracted at state 12 and saturated water at state 15. The latter As shown in Figure 14.14, the geothermal stream of the
stream is throttled from 300 to 200 kPa, yielding a saturated QFPP at state 20 provides heat to the VHTG of the QEAS.
liquid-vapor mixture at state 16, which enters the fourth steam In the VHTG, the strong solution from the absorber at state
separator. There, saturated steam is extracted at state 17 and 14 is heated and exits the VHTG as a weak solution at state
saturated liquid is extracted at state 20 and supplied to the 16 and as a high-concentration ammonia-water vapor at
0.4 0.08
0.3 0.06
0.2 0.04
270 275 280 285 290 295 300 305
Ambient temperature [K]
Chapter | 14 Exergy Analysis of Integrated Trigeneration and Multigeneration Systems 311
state 15. The weak solution at state 16 releases heat in the the MTG, and exits as ammonia-water vapor at states 21
VHHX and is combined with the weak solution from the and 22. These streams are combined, exit the MTG at state
HTG at state 20, to form the weak solution at state 35, 23, heat the strong solution from state 28 in the LTG, and
which in turn releases heat in the high-temperature heat exit as ammonia-water vapor at states 25 and 26. The vapor
exchanger (HHX) and is combined with the weak solution stream at state 26 passes to the condenser while that at state
from the MTG at state 24 to form the weak solution at 25 enters the condenser heat exchanger (CHX) and trans-
state 37. After releasing heat to the medium-temperature fers heat to part of the liquid that is fed in the opposite
heat exchanger (MHX), this weak solution is combined direction by the solution pump at state 3. This liquid gains
with the weak solution from the LTG at state 29 to form the heat and leaves the CHX at state 30. The ammonia-water
weak solution at state 39, which enters the low-temperature vapor exiting the CHX at state 27 is condensed to state 31
heat exchanger and heats the strong solution from the solu- in the condenser, warming the air flowing through the
tion pump at state 4. After heat transfer, the weak solution at condenser for use in heating the building. The vapor stream
state 40 passes through the expansion valve and enters the leaving the condenser at state 31 is throttled in the expan-
absorber at state 41. The refrigerant vapor exiting the VHTG sion valve to state 32 and enters the evaporator, where the
at state 15 then enters the HTG, where it heats the strong refrigeration load carried by the air flowing through
solution from the HHX at state 12 and then exits as the evaporator is absorbed by the QEAS refrigerant, and the
ammonia-water vapor at states 17 and 18. These streams are heated strong ammonia-water mixture exits the condenser
combined and exit the HTG at state 19. The combined at state 33 and enters the absorber. The part of the air stream
stream heats the strong solution from the MHX at state 9 in cooled in the evaporator is supplied to the drying process,
detrimental for countries with relatively high mean ambient therefore an increase in ambient temperature tends to
temperatures and advantageous for countries with lower increase the exergetic COP. However, the overall exergetic
mean ambient temperatures like Canada. But the air-drying utilization factor depicts a bell-shaped behavior, peaking
process uses cooling with dehumidification, so an increase at 0.33.
in ambient temperature necessitates greater cooling since it The variations with geothermal source temperature of
leads to increased heat gain by the system. Hence, an the energy and exergy efficiencies of the QFPP are presented
increase in ambient temperature degrades the performance in Figure 14.18. As the geothermal source temperature in-
of the cooling system. creases, the exergy efficiency increases but the energy effi-
Variations with ambient temperature of the exergetic ciency decreases slightly. The energy efficiency ranges from
COP of the QEAS and the exergetic utilization factor of 98.2% to 97.7% and exergetic efficiency from 27% to 37%, as
the overall system are shown in Figure 14.17. The exer- the geothermal source temperature rises from 425 C to
getic COP varies from 9.2 to 5.0 and the overall exergetic 500 C. Thus, the geothermal source temperature has
utilization factor from 0.005 to 0.33, as ambient air a significant impact on efficiency from an exergy perspec-
temperature increases, for condenser loads ranging from tive, but not from an energy perspective.
400 to 450 kW. An increase in ambient temperature and The manner in which the energetic and exergetic COPs of
condenser load therefore increases the exergetic COP of the absorption system vary with geothermal source temper-
the system. This beneficial effect is attributable to the fact ature is depicted in Figure 14.19. Both COPs increase with
that the condenser load is used as a heat supply and geothermal source temperature and condenser load. The
energetic COP varies from 4.0 to 5.4 and the exergetic COP source temperature and condenser load indicates that an
from 4.2 to 8.9. The exergetic COP is greater than the increase in geothermal source temperature improves the
energetic COP. Increasing the geothermal source temper- performance of the overall integrated system. But the
ature thus improves the performance of the absorption energetic and exergetic utilization factors differ little at
system from an exergetic point of view. The exergetic COP the considered conditions.
obtained is comparable to that for a conventional vapor-
compression system, but the system considered here has no
compressor consume electricity.
The variations with geothermal source temperature of
14.7 CLOSING REMARKS
the overall energetic and exergetic utilization factors are The importance of trigeneration and multigeneration systems
illustrated in Figure 14.20. The energetic utilization is highlighted in this chapter, as is the usefulness of exergy
factor ranges from 0.26 to 0.33 and the exergetic utili- analysis in assessing and improving such systems. The energy
zation factor ranges from 0.24 to 0.33 as geothermal and exergy analyses of trigeneration and multigeneration case
source temperature increases from 450 C to 500 C and studies suggest that trigeneration and multigeneration systems
condenser load increases from 400 to 450 kW. The enhance the productivity by generating multiple products
increase in both utilization factors with geothermal in a single process.