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1 Copyright 2008 by ASME
Proceedings of the ASME International Mechanical Engineering Congress and ExpositionIMECE2008
October 31 - November 6, 2008, Boston Massachusetts, USA
IMECE2008-68339
EXERGY ANALYSIS OF A SOLID OXIDE FUEL CELL-GAS TURBINEHYBRID POWER PLANT
Valentina AmatiUniversity of Roma1 La SapienzaDept. of Mechanical Engineering
Via Eudossiana 18, 00184, Rome, ItalyTel: +390644585272; E-mail:[email protected]
Enrico SciubbaUniversity of Roma1 La SapienzaDept. of Mechanical Engineering
Via Eudossiana 18, 00184, Rome, ItalyTel: +390644585244 ; E-mail:[email protected]
Claudia ToroUniversity of Roma1 La SapienzaDept. of Mechanical Engineering
Via Eudossiana 18, 00184, Rome, ItalyTel: +390644585272; E-mail:
ABSTRACT
The paper presents the exergy analysis of a natural gas fuelled
energy conversion process consisting of a hybrid solid oxide
fuel cell coupled with a gas turbine.
The fuel is partly processed in a reformer and then undergoes
complete reforming in an internal reforming planar SOFC
stack (IRSOFC). The syngas fuels in turn a standard gas
turbine cycle that drives the fuel compressor and generates
excess shaft power. Extensive heat recovery is enforced both
in the Gas Turbine and between the topping SOFC and the
bottoming GT.
Two different configurations have been simulated and
compared on an exergy basis: in the first one, the steamneeded to support the external and the internal reforming
reactions is completely supplied by an external Heat Recovery
Steam Generator (HRSG), while in the second one that steam
is mainly obtained by recirculating part of the steam-rich
anode outlet stream.
The thermodynamic model of the fuel cell system has been
developed and implemented into the library of a modular
object-oriented Process Simulator, Camel-Pro; then, by
means of this simulator, the exergetic performance of the two
alternative configurations has been analyzed. A detailed
analysis of the exergy destruction at component level is
presented, to better assess the distribution of irreversibilitiesalong the process and to gain useful design insight.
INTRODUCTION
Solid oxide fuel cells (SOFCs) are direct energy
conversion devices with great potential. The technology has
distinct features which makes it suitable for electric utility
power generation in both large central station power plants
and distributed generation units [11].
SOFCs are solid state, ceramic cells, characterized by the
highest operating temperature (600-1000C) among all types
of fuel cells under development. Their high operatingtemperature not only dispenses of the need for expensive
catalysts but also produces high quality heat which can be fed
to cogeneration or bottoming cycles for additional electricity
generation [16].
Because of the feasibility of integration of solid-oxide fuel cell
(SOFC) and gas-turbine (GT) technologies in power
generation, preliminary results predict that an overall system
efficiency of 70% (net ac/LHV) or higher is possible with a
more complex thermodynamic cycle [15],[20]. These studies
were mainly based on an energy analysis, combining the first
Law of Thermodynamics with a techno-economical
evaluation.
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The models of the SOFC sub-system (SOFC+Reformer) used
in this work have been developed and implemented by the
authors in the Camel Pro simulator, as described in a previous
work [2]. The fuel cell model developed in this study is of a
planar design: its geometric and material data are taken from
[1] .
The SOFC electrochemical performance is modeledconsidering all forms of overpotential: the zero-dimensional
model implemented herein calculates stack power and outlet
stream parameters at the stack temperature.
The hybrid system was modeled by means of macroscopic
energy and mass balances performed on each component.
1.1 SOFC/GT cycle
Figure 1 shows the plant layout of the simple SOFC/GT
hybrid system simulated with Camel Pro.
External pre-filtered input air (Stream 24) is first compressed
in the main process compressor (C1) and then preheated bythe turbine exhaust gas in a gas/gas heat exchanger (AHR2).
The fuel (natural gas, Stream 22) is compressed in the fuel
compressor (C2) and then preheated in the heat exchanger
(AHR1). The required steam (Stream 18) is generated in a heat
recovery Boiler (HRB) fed by the gas turbine hot exhaust.
The compressed and pre-heated fuel is partially reformed in
the reforming unit and then completely converted into a
hydrogen-rich gas within the internally reforming SOFC unit.
An external heat supply is required by the reformer to
maintain the desired operating temperature (Stream 2).
The air and the pre-reformed fuel enter the SOFC that
consumes hydrogen to produce power. The gas (cathode side
and anode side) at the cell outlet passes through a combustor
(CB), where the residual hydrogen (and carbon monoxide) in
the gaseous mixture is burned and expands in the gas
turbine(GT) to produce additional power.
The turbine exhaust gases are used to preheat fuel (AHR1),air (AHR2) and also provide the heat needed in the heat
recovery steam generator (HRB). The temperatures of both the
air and fuel exiting the SOFC are controlled by throttling the
inlet air flow.
1.2 SOFC/GT cycle with anodic gas recirculation
The second layout considered in this work is based on the
anode recirculation arrangement: the reforming reaction must
be driven by the use of steam, so in this case part of this steam
is obtained from the anode outlet stream. The latter must be
high enough to avoid problems of carbon deposition thatwould irreversibly damage the cell [6].
Figure 2 presents the scheme of the SOFC/GT hybrid system
with anodic gas recirculation.
Also in this case external pre-filtered input air (Stream 23) is
first compressed in the main process compressor (C1) and
then preheated by the turbine exhaust gas in a gas/gas heat
exchanger (AHR2).
The fuel, (natural gas, Stream 21) is compressed in the fuel
compressor (C2) and then preheated in the heat exchanger
(AHR1).
Figure 2 Camel Pro flow sheet of the SOFC/GT hybrid system with anode-recirculation flow sheet in
Air
Fuel
Water
Power
Power
Heat CC
RB
AHR1
AHR2GT
CP1
CP2
PUM
REFSOFC
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The compressed and pre-heated fuel stream is then mixed with
a part of the steam-rich high- temperature stream coming from
the cell anode outlet.
Since the adopted model prescribes the SC Ratio to be an
input parameter, the remaining steam required is calculated
taking into account also the steam content of the recirculated
flow.Methane is partially reformed in the reformer and the residual
CH4 is internally reformed at the SOFC anode.
An external heat supply is required by the reformer to
maintain the desired operating temperature (Stream 2).
Part of the steam-rich anode exhaust gas is recirculated to the
reformer inlet (Stream 29) and the remaining (Stream 13) is
mixed with the cathode exhaust gas (Stream 7) and channeled
into the combustion chamber (CC).
To reach the desired turbine inlet temperature, part of the fuel
at compressor outlet bypasses the SOFC group and enters
directly into the combustion chamber (Stream 14). After
combustion, the high temperature outlet gas (Stream 10) is
directed to the gas turbine. The turbine exhaust gas is used topreheat air (AHR2), fuel (AHR1) and the feed water (HRB).
2. EXERGY ANALYSIS
2.1 Exergy concepts
Exergy can be defined as the maximum amount of work which
can be obtained from a system or a flow of matter when it is
brought reversibly to equilibrium with the reference
environment.
Exergy analysis is based on the Second Law of
Thermodynamics and on the concept of irreversible entropyproduction. The exergy consumption during a process is
proportional to the entropy production due to irreversibilities.
In an exergy analysis, three forms of exergy transfer are
usually considered, i.e., exergy transfer by work-, heat- and
mass interaction.
For each sub-unit, the outlet exergy is always less than the
inlet exergy because of irreversible processes. When
calculating the exergy of a process component, the difference
between the exergy losses and exergy destruction are
recorded. Exergy losses include the exergy flowing to the
surroundings, whereas exergy destruction indicates the loss of
exergy within the system boundary due to irreversibility.
The exergy of a stream of matter can be divided into differentcomponent exergies. In the absence of nuclear, magnetic,
electrical and surface tension effects, exergy is calculated as
the sum of :
K P Ph ChEx Ex Ex Ex Ex= + + + (1)
where ExK, ExP , Exth and Exch are the kinetic, potential,
physical and chemical exergy respectively.
The changes in the kinetic and gravitational potential energies
are neglected in the present study.
Physical exergy is defined as the maximum amount of work
which can be obtained when a stream of matter is brought
from its initial state to the environmental state while only
exchanging heat with the thermal reservoir of the
environment, whereas chemical exergy is defined as the
maximum amount of work which can be obtained when the
stream of matter is brought from the environment state to thetotal dead (unrestricted) state as a result of heat transfer and
exchange of substances only with the environment.
( ) ( )0 0 0PhEx h h T s s= (2)
0
0 , lnch i i i ch iEx R T x x x ex= + (3)
where xi is the mole fraction of the species i in the flow and
exch,i0
is the molar chemical exergy of the ith
species.
In order to identify and quantify irreversibilities and losses in
energy quality, an exergy analysis of the two SOFC/GT plants
was performed. The modular process simulator calculates theexergy associated to each energy and material stream in the
plant and provides the values of the exergy destruction,ExD
and of the exergy efficiency,ExEff, of each component.
2.2 Streams
Electricity
The exergy content of the electricity is equal to its energy
content:
[ ]Elec ElecEx W kW= (4)
Gas Mixture and Steam
The specific exergy of gas mixture, exgas is the sum of its
physical (exph) and chemical exergy (exch), calculated as
follows:
[ / ]gas ph chex ex ex kJ kg= + (5)
0 0 0( ) ( ) [ / ]phex h h T s s kJ kg= (6)0
, ln[ / ]
i i i ch ni
ch
gas
R T n n n exex kJ kg
MW
+= (7)
Where the subindex 0 denotes reference conditions and the
exch0 for each species are tabulated in [19].
2.3 Components
The equations used to calculate ExD and ExEff, for each
component of the SOFC/GT plant are reported below.
Reformer
0
Ref
1 [ ]i i i i o oF F W W i w w
TExD m ex m ex Q m ex kW
T
= + +
(8)
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Sys
TotI
Fuel Fuel in
W
m LHV Q =
+(24)
The fuel utilization factor of SOFC is defined as:
( )2 44f i i iz
UH CO CH
=+ + (25)
where each CH4 mole generates 4 H2 moles (3 by the internal
reforming and 1 by the water-gas shift reaction). The variable
z is the number of H2 moles which are oxidized within the
SOFC. The power output of systems investigated are reported
in Table 4 and Table 5 together with the power needed by the
air and fuel compressors, the pump and the thermal power
required by the reformer. The two systems have been analyzed
for the same total SOFC electric current. From Tables 4 and 5
it is possible to calculate the efficiency: values of 65.4 % are
obtained for the standard SOFC/GT system and of 66.4 % for
the anode-recirculation one (as reported in Table VI).
Table 2 SOFC/GT: Power flows within the system
Sofc Electric Power
Id P Current Voltage
- kW A V
8 284.84 410060 0.728
Shaft Power
Id P n
- kW rpm
13 151.81 300017 0.0075 3000
23 2.2401 3000
25 55.094 3000
26 149.57 3000
27 94.478 3000
Reformer Heat
Id P
- kW
2 78.986
Thus the introduction of the anode-recirculation actuallyincreases the electrical efficiency because it allows to reduce
both the amount of heat required by the reformer and the
amount of external water needed.
On the basis of the results of the simulations, the First Law
efficiency of the two alternatives have been compared (Table
6): the cycle with anode-recirculation has a higher efficiency,
due to a lower heat request by the reformer even if the SOFC
electrical efficiency is lower.
In fact in this cycle the fuel entering the SOFC, obtained by
mixing a 50% of anode outlet gas with CH4 extracted from the
compressor, is more diluted and contains 37% of CO2.
In the SOFC/GT with anode-recirculation the system outlet
gas (Stream 14) consists of 13% O2, 73% N2, 6% CO2, 7%
H2O at 508 K while in the fundamental one has almost the
same composition at 435 K.
3.2 Second law analysis of results
The purpose of this work was to perform an explicit exergy
analysis of the plant, and to identify -for each process
configuration- the components affected by the highest
irreversible losses, so that a more accurate analysis could be
made in the design phase. In fact, an exergy analysis provides
the designer with better insight as to where a design
modification is necessary, both at the single component and at
a process level, to better exploit the available resources.
Table 3 SOFC/GT with anode recirculation : Power flows
within the system
The exergetic efficiency of the system is defined as:
,, ,
Sys
Ex SysFuel in Q in
W
Ex Ex=
+ (26)
The exergy analysis of the plants (Table 7 and Table 8 ) shows
a net exergy efficiency of 63.2% and 64.4% for the first
configuration and for the one with anode-recirculation
respectively.
In the standard SOFC/GT plant the exergy entering the system
(fuel and heat) amounts to 600 kW, the overall destroyed
exergy rate to 164 kW and the exergy loss to 56.75 kW thus
the net generation is 380 kW. In the alternative configuration
the exergy input is 531 kW, the overall destroyed exergy rate
Sofc Electric Power
Id P Current Voltage
- kW A V
8 264.561 410060 0.672
Shaft Power
Id P n
- kW rpm
12 135.074 3000
16 0.00114 3000
22 2.081 3000
24 55.094 300025 132.99 3000
26 77.89 3000
Reformer Heat
Id P
- kW
2 9.978
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0% 5% 10% 15% 20% 25% 30% 35% 40%
REF
SOFC
CC
GT
HRB
PUM
AHR1
AHR2
Cfuel
Cair
ExD%
ExFD%
Figure 5 Exergy destruction distribution in the SOFC/GT
cycle.
0% 5% 10% 15% 20% 25% 30% 35% 40% 45%
REF
SOFC
CC
GT
HRB
PM
AHR1
AHR2
CAir
CFuel
FM1
FM2
ExFD%
ExD%
Figure 6 Exergy destruction distribution in the SOFC/GT
cycle with anode recirculation.
Figure 7 Grassmann diagram of SOFC/GT system
Figure 8 Grassmann diagram of SOFC/GT system with anode-recirculation
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Figures 3 and 4 show the exergy efficiency of each component
for both processes. The SOFC has an exergy efficency of
83.4% in the standard plant and of 81.55% in the alternative
one.
Figures 5 and 6 clearly show that in either case the SOFC is
the component affected by the highest degree of irreversibility.Within the SOFC, in fact, most of the chemical reactions
occur, like steam reforming and electrochemical oxidation of
hydrogen. It is well known that these processes are the most
important source of irreversibilities. The distribution of
irreversibilities between the SOFC and the CC can be
modified by changing the fuel utilization factor. When the
value of Uf is very high almost all chemical processes take
place in the SOFC increasing its contribution to the global
irreversibilities. The opposite occurs for lower values of Uf(Figure 9).
Figure 7 and Figure 8 show the Grassmann diagrams for both
plant configurations. The diagrams show very clearly theprogressive build-up of exergy destruction from the input to
the output of the plant and the different contributions of each
component to the total exergy destruction.
0
10
20
3040
50
60
70
80
90
100
0.55 0.65 0.75 0.85 0.95
Uf
ExD
kW
ExD SOFC
ExD CC
ExD SOFC (Rec)
ExD CC (Rec)
CONCLUSIONS
This paper presented an exergy analysis of a hybrid SOFC/GT
power plant. A standard plant configuration was compared to
an alternative one provided with anode-outlet gas re-
circulation. Although the fuel cell per se is a rather efficient
device, it is the most important source of exergy destruction
in the cycle. The other main source of irreversibility is -as
expected- the combustion chamber. The results show that
anode gas recirculation leads to an increase in both the energy
and exergy efficiency of the system, from 65.6 % to 66.4 %
(First Law) and 63.6% to 64.4% (Second Law) respectively.
In addition, the recirculating option reduces by 85% the
feedwater needed and by 88% the high-T heat required by the
reformer.
.
NOMENCLATURE
ex specific exergy [kJ/kg]
ExD destroyed exergy [kW]
ExEff exergetic efficiency
Fi input syngas stream
Fo output syngas stream
Gi input air stream
Go output air stream
h specific entalphy [kJ/kg]
ITOT SOFC electric current [A]
LHV lower heating value [kJ/kg]
m& mass flowrate [kg/s]
ni molar fraction of ith specie
Q heat flow [kW]
R universal gas constant [J/molK]
s specific entropy [kJ/kg/K]
Si input steam or water stream
So output steam or water stream
SC steam-to-carbon ratio
T temperature [K]
TIT turbine inlet temperature [K]
Ua SOFC oxygen utilization factor
Uf SOFC fuel utilization factor
V potential [V]
W Power [kW]
SOFC SOFC electrical efficiency
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