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Fuel cell cathode air filters: Methodologies for design and optimization
Daniel M. Kennedy a , Donald R. Cahela a , Wenhua H. Zhu a , Kenneth C. Westrom b ,
R. Mark Nelms b , Bruce J. Tatarchuk a,∗
a Center for Microfibrous Materials Manufacturing, Department of Chemical Engineering, Auburn University, AL 36849, USA
b Department of Electrical and Computer Engineering, Auburn University, AL 36849, USA
Received 14 December 2006; received in revised form 8 March 2007; accepted 9 March 2007
Available online 19 April 2007
Abstract
Proton exchange membrane (PEM) fuel cells experience performance degradation, such as reduction in efficiency and life, as a result of poisoning
of platinum catalysts by airborne contaminants. Research on these contaminant effects suggests that the best possible solution to allowing fuel cells
to operate in contaminated environments is by filtration of the harmful contaminants from the cathode air. A cathode air filter design methodology
was created that connects properties of cathode air stream, filter design options, and filter footprint, to a set of adsorptive filter parameters that must
be optimized to efficiently operate the fuel cell. Filter optimization requires a study of the trade off between two causal factors of power loss: first, a
reduction in power production due to poisoning of the platinum catalyst by chemical contaminants and second, an increase in power requirements
to operate the air compressor with a larger pressure drop from additional contaminant filtration. The design methodology was successfully applied
to a 1.2 kW fuel cell using a programmable algorithm and predictions were made about the relationships between inlet concentration, breakthrough
time, filter design, pressure drop, and compressor power requirements.
© 2007 Elsevier B.V. All rights reserved.
Keywords: Cathode air filter; PEM stack contaminant; PEFC filter design
0378-7753/$ – see front matter © 2007 Elsevier B.V. All rights reserved.
doi:10.1016/j.jpowsour.2007.03.020
392 D.M. Kennedy et al. / Journal of Power Sources 168 (2007) 391–399
together with the adsorptive filter parameters: saturation capac- of the filter by affecting contacting regimes as well as pressure
ity, removal efficiency, and pressure drop. These parameters then drop. Lastly, the filter footprint affects all three filter parameters
influence the PV work required to operate the compressor at the through bulk design.
desired air flow rate and the stack efficiency defined by the poison
tolerance and lifetime. 3.2.5. Compressor attributes
Once the adsorptive filter parameters have been established,
3.2.1. Inlet air properties their effect on the compressor can be established. Pressure drop
The inlet air properties, along with the stack attributes, dic- across the filter causes a decrease in inlet pressure (P1 ) to the
tate the efficacy and capability that the filters must possess. compressor creating a vacuum. The outlet pressure (P2 ) from the
Air properties affect filter parameters by defining the capac- compressor is set by the required flow rate necessary to oper-
ity and removal efficiency needed to remove contaminants to ate the fuel cell. This increase in pressure ratio (P2 /P1 ) across
achieve a specified output level. Single pass removal efficiency the compressor causes a decrease in compressor efficiency and
is increased by reducing adsorbent particle size thereby increas- an increase in compressor power. Both of these effects cause
ing surface area and eliminating intra-particle mass transport. an overall decrease in fuel cell operating efficiency and perfor-
High single pass removal efficiency results in a filter effective at mance.
removal of contaminates at low concentrations. An increase in
either the capacity or the removal efficiency results in an increase 3.2.6. Fuel cell stack attributes
in both filter pressure drop and the amount of power required by The fuel cell stack is also affected by variations in the fil-
the compressor. ter parameters. The stack has a certain tolerance and operating
lifetime related to the concentration of contaminants passing
3.2.2. Filter design options through the cathodes of the cells. The filter controls this con-
While many filter design options exist, for this research three centration by reducing the contaminant concentrations before
options are considered: packed bed (PB), microfibrous mate- they make contact with the cathode. The single pass removal
rials (MFM), and composite bed (MFM + PB). A packed bed efficiency required is dictated by the maximum concentration
is the most widely used form of filtration. Packed bed charac- tolerable by the fuel cell. The maximum concentration may be
teristics include high sorbent capacity, low single pass removal lower if the contaminant collects in the stack rather than passing
efficiency, and low pressure drop. The second design option, through the exhaust.
microfibrous materials, has been proven effective with high log
and high single pass removal of chemical contaminants, but has 3.3. Cathode air filter optimization: a trade off between
a lower capacity and higher pressure drop when compared to compressor power requirements and efficiency losses from
packed beds. Microfibrous materials also add a new dimension catalysts poisoning
to the problem, through application as a pleated filter media, or
as a polishing sorbent in a composite bed formation [5]. Pleated Research on cathode durability has concluded that the effect
microfibrous materials have an increased capacity and lower that contaminants have on fuel cell performance varies depend-
pressure drop than a flat sheet with a smaller area. A composite ing on the contaminant type and concentration, leading to three
bed effectively combines the capacity of a packed bed and the different scenarios for contaminant remediation. In the first sce-
high contacting efficiency of microfibrous materials. An opti- nario, contaminants have little to no permanent effect, and do not
mized composite bed is capable of higher logs of removal, has build up in the system, so can be ignored. For example, it may
a reduced total bed depth, and has a lower pressure drop than a be more acceptable to allow a small percentage of contaminant
packed bed. through, rather than to increase filtration, thereby resulting in a
higher pressure drop. An example of this would be CO, where
3.2.3. Filter footprint the damaging effect is both small and temporary.
Another category that needs to be considered for its effect on In the second scenario, contaminants need to be completely
filter parameters is the filter footprint. An increase in area allows removed, because any amount of exposure to the contaminant
for a decrease in thickness and visa versa. In many cases, the will cause a permanent degradation of fuel cell performance.
footprint may be set by the fuel cell system in order for the filter to These contaminants build up in the system, causing more severe
be retrofitted into the existing particulate filter slot. Filter weight degradation with longer exposure times. For example, a cathode
affects the filter capacity and is required for analysis because of air filter must be capable of removing sulfur compounds such as
the differences in densities of the filter design options. H2 S and mustard gas (C4 H8 Cl2 S).
In the third scenario, contaminants must be removed to a
3.2.4. Adsorptive filter parameters point of maximum concentration to minimize a decrease in fuel
Inlet air properties, filter design options, and filter footprint cell performance. A decision for further removal beyond this
all relate to the adsorptive filter parameters. Contaminant type, defined maximum must take into account the effect the increase
concentration, and flow rate affect the filter parameters by virtue in filter pressure drop will have on the system. For example, SO2
of the differences in chemical properties that various contami- at concentrations of 2.5–5 ppm has a significant effect on fuel
nants have in relation to the filter adsorptive materials. Filter cell performance, with as much as a 50–60% reduction in fuel
design options control the mass and energy transport properties cell power [4]. This situation would clearly require a cathode
394 D.M. Kennedy et al. / Journal of Power Sources 168 (2007) 391–399
air filter for efficient fuel cell operation. SO2 concentrations of An exact breakthrough equation for non-reversible adsorp-
lower than 0.5 ppm may be ignored completely as they have tion onto a surface can be applied to a single or dual layer bed. Eq.
no noticeable effect [2], so a cathode air filter would not be (2), derived by Amundson [8], is based on mass balance across an
necessary. However, at moderate concentrations, between 1 and adsorptive bed allowing for a time varying input concentration.
! " t−(εz/v0 ) #
C C0 (t − (εz/v0 )) exp ε(k/v0 ) 0 C0 (η) dη k
= ! "z # ! " t−(εz/v0 ) # , t≥ε (2)
C0 exp ε(k/v0 ) 0 (N0 − n(ξ)) dξ + exp ε(k/v0 ) 0 C0 (η) dη − 1 v0
Table 1
Quantitative fuel attributes used in the algorithm
Input parameter Parameter value
Table 2
Filter design input parameters collected from experimental data
Design parameter Microfibrous layer Packed bed
Filter capacity (N0 ) 0.04 moles hexane cm−3 0.1 moles hexane cm−3
Adsorption rate (k$ ) 0.00332C0 0.00183C0
Voidage (ε) 0.772 0.4
Air flow rate 89.5 LPM 89.5 LPM
Pressure drop 0.0664L2 v0 0.0514L1 v0
Fig. 4. Programmable design algorithm. Compressor power 313.14(P2 /P1 ) − 312.74 313.14(P2 /P1 ) − 312.74
For each case study and each breakthrough time tested, the
composite bed was optimized to minimize total bed depth. This
was accomplished by varying the thickness of the packed bed,
calculating the required thickness of the microfibrous layer, and
calculating the total thickness. Table 3 shows the individual layer
Fig. 8. Predicted thickness required to meet breakthrough time requirements. thicknesses for each of the breakthrough times in the case study.
398 D.M. Kennedy et al. / Journal of Power Sources 168 (2007) 391–399
Table 3
Predicted, optimized individual layer thicknesses of the packed bed (L1 ) and microfibrous layer (L2 ) used to create a composite bed
Time (min) Case I Case II Case III
100–5 ppm (1.3 logs removal) 10–0.1 ppm (2 logs removal) 100–0.1 ppm (3 logs removal)
By studying these graphs, information can be learned about shows a sharper breakthrough. A shallower breakthrough curve
the capacity and removal efficiency requirements of the filter results from a lower contacting efficiency than predicted. Since
and how filter configurations are affected by inlet concentration, contacting efficiency is primarily a factor of adsorption rates the
outlet concentration, and breakthrough time. inaccuracy in the breakthrough curve is caused by inaccuracy in
Cases I and III require the thickest packed bed portion due the determination of the adsorption rate values. The filter capac-
to the fact that they have the higher capacity requirements of 95 ity is only slightly overestimated by the algorithm and as a result
and 99.9 ppm removal, respectively, when compared 9.9 ppm the breakthrough is sooner than predicted.
removal requirement for Case II. Secondly, the thickness of Pressure drop predictions, shown in Fig. 11, were accurate at
the microfibrous layer increases with log removal requirements. flow rates lower than 70 SLPM when compared to experimen-
This is a result of the higher single pass removal efficiency tally determined data. At higher flow rates actual pressure drop
required for high log removal. was higher than predicted. This may be due to inertial losses
Further analysis is performed by moving down the columns which cause a non-linear pressure drop relationship when oper-
and considering higher breakthrough time requirements. By ating at higher flow rates and was assumed negligible when the
increasing breakthrough time, additional capacity is required to pressure drop formula was determined for a packed bed.
meet the breakthrough requirements. This results in an increase
in the thickness of the packed bed layer of the filter. However, 7.2. Pleated microfibrous filter
at low breakthrough times, where capacity is less significant, a
thicker microfibrous layer provides a shorter overall bed depth Fig. 12 shows breakthrough curves predicted by the algo-
by reducing the critical bed depth (the minimum bed depth rithm compared with those found experimentally. In this case,
required to prevent immediate breakthrough). the breakthrough was 15 min sooner than predicted, indicating
that the capacity was overestimated. Adsorption rate values were
7. Filter tests results more accurate, evident by the similar shape of the sigmoidal
breakthrough curve for both the actual and predicted curves.
7.1. Composite bed filter Pressure drop predictions for the pleated filter, shown in Fig. 13,
are higher than actual values. A small percentage of this differ-
Fig. 10 shows the results of the 100 ppm challenge break- ence in pressure drop is a result of leaks in the filter and can be
through test on the composite bed filter. Breakthrough at 0.1 ppm resolved with better construction techniques. A small curvature
was 27 min. Predicted value was 100 min. The predicted curve in the actual pressure drop is the result of inertial losses due to
the air having to pass through the pleats. Inertial losses were
Fig. 10. Actual breakthrough curves for composite bed compared to a predicted Fig. 11. Pressure drop comparison between a composite bed filter and values
breakthrough curve by the algorithm. predicted by the algorithm.
D.M. Kennedy et al. / Journal of Power Sources 168 (2007) 391–399 399
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