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Fuel Cells
Module 3 (Final Draft): Energy Balance in a Solid Oxide Fuel Cell
Module Author: Donald J. Chmielewski
Module Affiliation: Center for Electrochemical Science and Engineering
Department of Chemical and Biological Engineering
Illinois Institute of Technology, Chicago, IL 60616
Background/Introduction
Fuel cells are a promising alternative energy conversion technology. One type of fuel cell,
the Solid Oxide Fuel Cell (SOFC) uses hydrogen as a fuel. The fuel reacts with oxygen to
produce electricity. Fundamental to SOFC design is an understanding of the heat
generated by the reaction and its impact on efficiency.
H2 Air
In In
Anode Cathode
Fuel Cell
Gas
Chamber
Gas
Chamber
H2 &
H2O Air
Out Out
e-- e--
N
N22
H
H22 O
O22
O2-2-
O
H
H22O
O O
O22
N
N22
H
H22
H
H22 O
O22
O2-2-
O
H
H22O
O
N
N22
H O H
H22O H22
O2-2-
O
O
O22
O
O22
H22 H
H H22O
O O2-2-
O
Anode
Anode Cathode
Cathode
Electrolyte
Electrolyte
For each mole of hydrogen consumed, two moles of electrons are passed through the
electric load. To convert electron flow, Faradays constant should be used ( F 96,485
coulombs/mole of electrons). The objective of a fuel cell is to deliver power to the load:
Power = Current Voltage. ( coulomb volt joule and joule / s watt ). The fuel cell
obtains this power from the enthalpy released during the overall reaction H2 + 1/2O2
H2O; however, only a portion of this enthalpy can be converted to electric power, the
remainder will appear as heat released by the reaction. This heat must be removed using
the flowing gas streams. The performance of a fuel cell is typically communicated in
terms of efficiency, defined as energy delivered to the load divided by the energy
available from reaction.
Problem Information
Example Problem Statement: An adiabatic SOFC is operated at atmospheric pressure
with an inlet flow of pure hydrogen at 20 g/s and a hydrogen utilization of 75%. The term
utilization is synonymous with the percent conversion, as defined in Section 4.6 of Felder
and Rousseau (2000). At the cathode chamber inlet, 2.67x10 5 standard liters per minute
(slpm) of air is fed at 500oC, and the gas exiting the cathode chamber is at 625 oC. If the
exit stream of the anode chamber is 675oC and the cell voltage is 0.7 volts, then
determine the following:
1) To determine power to the load we must first determine current to the load and
combine with cell voltage (given to be 0.7 volts). Since current is proportional to the rate
of electrons generated by the half reaction (here we will use the anode reaction), we must
first determine the conversion rate for the anode reaction. If 75% of the hydrogen is
utilized, then the conversion rate, , is found as:
This rate along with the anode stoichiometry (2 mole of electrons per mole of H2)
indicate that 15 moles/s of electrons must be delivered to the load. If we now use
Faradays constant as a unit conversion, we find the current to be (15 mole of electrons/s)
x (96485C/mole of electrons) = 1.45x106 amps. This current multiplied by the cell
voltage (0.7 volts), gives the load power as 1MW. In the notation of chapter 7 of Felder
and Rousseau (2000), this power should be considered shaft work being removed from
(or being done by) the system.
2) The molar flow out of the cathode is equal to the molar flow into the cathode minus
the molar flow of oxygen through the electrolyte and into the anode. We start by
calculating the molar flow into the cathode. Assuming air is an ideal gas at standard
conditions (1 atm and 0oC), we find that the number of moles per standard liter is:
n P 1 atm
0.045moles / L
V RT 0.08206L atm mol 1 K 1 273K
Using the reaction stoichiometry and our calculation that 7.5 moles/s of H2 are reacted in
the anode, we conclude that 3.75 moles/s of O2 are reacted in the cathode. Thus, the exit
flow from the cathode must be 200.25 - 3.75 = 196.5 moles/s.
3) Now that we have performed some initial calculations concerning material and energy
flows, we turn to the energy balance of the entire system. After identifying the
appropriate balance equation, we find the need to calculate the reaction generated
Since the SOFC is a continuous (or open) process, we should apply Equation 7.4-15 of
Felder and Rousseau (2000):
H W
E E Q (7.4-15)
k p in shaft , out
Neglecting E , E and Q , the last being p due to assumption of adiabatic operation,
k in
leaves:
W
H (E-1)
shaft , out
H H ro n H n H
outlet
i i
inlet
i i (9.5-1a)
From part (1) we have that W shaft ,out =1MW. Then using Table B.1 of Felder and
Rousseau (2000) for the reaction H2 + 1/2O2 H2O(g), we find the enthalpy of reaction, (
H ro ), to be -241.8 kJ/mole of H2 converted. Combining this with the conversion rate
we find:
Applying this to Equation 9.5-1a and combining with Equation E-1 gives:
1MW 1.8MW n H
outlet
i i n i H i
inlet
or
0.8MW n H
outlet
i i n i H i
inlet
n H 2 ,out H H 2 , Ta , out n H 2O ,out H H 2O , Ta ,out n N 2 ,out H N 2 , Tc , out n O2 ,out H O2 , Tc , out
n H 2 ,in H H 2 , Ta ,in n N 2 ,in H N 2 , Tc ,in n O2 ,in H O2 , Tc ,in
(The subscripts of T correspond to a for anode c for cathode in for inlet and out for
outlet.) Since we know all of the molar flows into and out of the system, each of the n i
terms is known. Summarizing from parts (1) and (2), we have
Additionally, we can utilize Table B.8 of Felder and Rousseau (2000) to determine H i for
all of the streams except for the inlet to the anode, since temperature of this stream is not
known. (Linear interpolation used whenever needed.)
This gives:
800 kJ / s n H
outlet
i i n i H i
inlet
n H 2 ,out H H 2 , Ta ,out n H 2O ,out H H 2O , Ta ,out n N 2 ,out H N 2 , Tc ,out n O2 ,out H O2 , Tc ,out
n H 2 ,in H H 2 , Ta ,in n N 2 ,in H N 2 , Tc ,in n O2 ,in H O2 , Tc ,in
2.5 19.0 7.5 23.9 158.2 18.2 38.3 19.3
10 H , 158.2 14.2 42.05 15.0
H 2 Ta , in
Solving this equation for H H ,T , yields 16.8 kJ/mole H2. From Table B.8 of Felder and
2 a ,in
Rousseau (2000), this enthalpy is achieved at 600oC, which would need to be the inlet
temperature to the anode. (It should also be noted that implicit in our application of
Equation 9.5-1a, we have used 1 atm and 25oC as the reference state, which was dictated
by the data received from Tables B.1 and B.8 of Felder and Rousseau (2000).)
4) If we define cell efficiency as the ratio of useful power to chemical energy input, we
find
This assumes the un-utilized hydrogen can be recycled. If not, and we are assuming the
un-utilized hydrogen is lost, then a more appropriate efficiency value would be based on
total conversion of the hydrogen, = 10 mole of hydrogen converted / s. The result of
this assumption is be to calculate H ro as (10 mole/s of H2) x (-241.8 kJ/mole H2),
which gives the new efficiency as:
An atmospheric pressure, adiabatic SOFC is operated with the following inlet and exit
conditions: