CA1270897A - Fuel cell powerplant employing an aqueous solution - Google Patents
Fuel cell powerplant employing an aqueous solutionInfo
- Publication number
- CA1270897A CA1270897A CA000511820A CA511820A CA1270897A CA 1270897 A CA1270897 A CA 1270897A CA 000511820 A CA000511820 A CA 000511820A CA 511820 A CA511820 A CA 511820A CA 1270897 A CA1270897 A CA 1270897A
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- Canada
- Prior art keywords
- conduit
- water
- powerplant
- hydrous oxide
- fuel cell
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04029—Heat exchange using liquids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Sustainable Development (AREA)
- Sustainable Energy (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Compounds Of Iron (AREA)
- Fuel Cell (AREA)
Abstract
Abstract A fuel cell powerplant 10 having a flow path 20 for an aqueous solution includes a device 18 for disposing in the solution ferric hydrous oxide of a character that retards the deposition of iron based compounds. The device is disposed within the powerplant and receives water from a conduit 42 which communicates with a component of the fuel cell powerplant, such as a fuel cell stack 12.
Description
12~ 7 Description Technical Field This invention relates to fuel cell power-plants which use an aqueous solution as a working medium. The working medium may be used to remove heat from components or to produce steam for pro-cessing raw fuel. Although this invention was devel-oped for use in the field of fuel cell powerplants, the invention may have application in any field employing aqueous solutions that deposit lron based compounds on the walls of the conduit.
Brief Description of Drawings Fig. 1 is a schematic representation of an actual fuel cell powerplant having a cooling system which uses an aqueous solution as a coolant and as a source of steam and further shows an auxili-ary system for supplying type II ferric hydrous oxide to the powerplant under operative conditions.
Fig. 2 is a graphical representation of the equivalent diameter Dea of the fuel cell stack versus run time under operative conditions without - the addition of type II ferric hydrous oxide; the equivalent diameter is normalized by dividing by the initial equivalent diameter Dei.
Fig. 3 is an enlarged, cross-sectional view of an orifice used in the cooling system of Fig. 1.
Fig. 4 is an alternate embodiment of the fuel cell powerplant shown in Fig. 1.
Fig. 5 is an enlarged schematic representa-tion of a portion of the powerplant shown in Fig.
4.
Fig. 6 is a graphical representation of the equivalent diameter Dea versus run time under operative conditions with the addition of type II
ferric hydrous oxide; the equivalent diameter is nor-malized by dividing by the initial equivalent diameterDei.
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1271~8~7 Background of Invention Fuel cell powerplants produce electric power by electrochemically consuming a fuel and an oxidant in one or more electrochemical cells. The oxidant may be pure oxygen or a mixture of gases containing oxygen, such as air. The fuel may be hydrogen. One source of hydrogen is a fuel processor that reforms natural gas or any appropriate hydrocarbon by using heat and steam to crack hydrocarbons.
Typically, a stack of fuel cells is used in performing the electrochemical reaction. During the electrochemical reaction, the fuel cell stack produces electric power, a reactant product and waste heat. A cooling system removes waste heat from the stack. The cooling system may advantageously use an aqueous coolant to provide both waste heat and water (as steam) to the fuel processor.
The cooling system includes flow paths for the aqueous coolant which are bounded by conduits.
The conduits extend to the steam separator and to the fuel cell stack for ducting the coolant to critical locations. These conduits may have small orifices for controlling the distribution of coolant throughout the cooling system.
One problem with aqueous coolants is the cumulative deposition of particles on the walls of conduits. The particles may occur as ions or as minute parts of matter. The particles, which are capable of accumulation to the point of blockage, are generally iron based compounds. These iron based compounds are composed mainly of iron based oxides, such as magnetite and hematite, iron based salts, such as iron phosphates, and other compounds which result from the corrosion of iron including certain ferric hydrous oxide particles (hereinafter type I
ferric hydrous oxide). The iron based compounds may form as the coolant comes in contact with materials 1~7~P8~
containing iron. Such contact might occur as the coolant is flowed through conduits in the powerplant or through supply conduits to the powerplant.
The problem is particularly troublesome for cooling systems using small orifices because the particles may block the orifices. Any blockage of an orifice in a fuel cell stack, for example, will increase the flow resistance through the stack and may even cause an inadequate supply of coolant to a critical location within the fuel cell stack.
One way of establishing the effect of such deposition on flow resistance through the stack is to treat the supply conduits of the fuel cell stack as if they were an equal number of equally sized ideal orifices. The diameter of these equally sized orifices is called the equivalent diameter of the fuel cell stack. The equivalent diameter may be found experimentally as follows:
1. Establish a constant flow rate of coolant through the fuel cell stack.
Brief Description of Drawings Fig. 1 is a schematic representation of an actual fuel cell powerplant having a cooling system which uses an aqueous solution as a coolant and as a source of steam and further shows an auxili-ary system for supplying type II ferric hydrous oxide to the powerplant under operative conditions.
Fig. 2 is a graphical representation of the equivalent diameter Dea of the fuel cell stack versus run time under operative conditions without - the addition of type II ferric hydrous oxide; the equivalent diameter is normalized by dividing by the initial equivalent diameter Dei.
Fig. 3 is an enlarged, cross-sectional view of an orifice used in the cooling system of Fig. 1.
Fig. 4 is an alternate embodiment of the fuel cell powerplant shown in Fig. 1.
Fig. 5 is an enlarged schematic representa-tion of a portion of the powerplant shown in Fig.
4.
Fig. 6 is a graphical representation of the equivalent diameter Dea versus run time under operative conditions with the addition of type II
ferric hydrous oxide; the equivalent diameter is nor-malized by dividing by the initial equivalent diameterDei.
, .
t .-' ~
1271~8~7 Background of Invention Fuel cell powerplants produce electric power by electrochemically consuming a fuel and an oxidant in one or more electrochemical cells. The oxidant may be pure oxygen or a mixture of gases containing oxygen, such as air. The fuel may be hydrogen. One source of hydrogen is a fuel processor that reforms natural gas or any appropriate hydrocarbon by using heat and steam to crack hydrocarbons.
Typically, a stack of fuel cells is used in performing the electrochemical reaction. During the electrochemical reaction, the fuel cell stack produces electric power, a reactant product and waste heat. A cooling system removes waste heat from the stack. The cooling system may advantageously use an aqueous coolant to provide both waste heat and water (as steam) to the fuel processor.
The cooling system includes flow paths for the aqueous coolant which are bounded by conduits.
The conduits extend to the steam separator and to the fuel cell stack for ducting the coolant to critical locations. These conduits may have small orifices for controlling the distribution of coolant throughout the cooling system.
One problem with aqueous coolants is the cumulative deposition of particles on the walls of conduits. The particles may occur as ions or as minute parts of matter. The particles, which are capable of accumulation to the point of blockage, are generally iron based compounds. These iron based compounds are composed mainly of iron based oxides, such as magnetite and hematite, iron based salts, such as iron phosphates, and other compounds which result from the corrosion of iron including certain ferric hydrous oxide particles (hereinafter type I
ferric hydrous oxide). The iron based compounds may form as the coolant comes in contact with materials 1~7~P8~
containing iron. Such contact might occur as the coolant is flowed through conduits in the powerplant or through supply conduits to the powerplant.
The problem is particularly troublesome for cooling systems using small orifices because the particles may block the orifices. Any blockage of an orifice in a fuel cell stack, for example, will increase the flow resistance through the stack and may even cause an inadequate supply of coolant to a critical location within the fuel cell stack.
One way of establishing the effect of such deposition on flow resistance through the stack is to treat the supply conduits of the fuel cell stack as if they were an equal number of equally sized ideal orifices. The diameter of these equally sized orifices is called the equivalent diameter of the fuel cell stack. The equivalent diameter may be found experimentally as follows:
1. Establish a constant flow rate of coolant through the fuel cell stack.
2. Measure the pressure drop through the fuel cell stack.
3. Calculate an equivalent diameter for the stack ~or any system) by the equation De= 2.8 (W2 / ~PN2d)l/4 10-7 where:
De = Effective Diameter, inches;
W = Total Coolant Flow (pound per hour);
d = Coolant Density (pounds per cubic foot);
N = Number of Conduits in Cell Stack;
~P = Differential Coolant Pressure Across Cell Stack (pounds per square inch, difference) ~27~8~7 Fig. 2 is an example of the effect such depositions can have on the equiv~lent diameter of a fuel cell stack under actual operative conditions.
After twenty-five hundred hours of operation (curve A) the actual equivalent diameter Dea was less then seventy percent of the initial equivalent diameter Dei. The decrease in size and the resulting decrease in the flow rate of coolant required a shutdown of the fuel cell stack for cleaning.
The fuel cell stack was cleaned after this period of operation by flowlng a pressurized, acidic solution through the conduits. Cleaning restored the actual equivalent diameter Dea to ninety-five percent of the initial effective diameter Dei (curve B).
After another twenty-two hundred hours of operation (curve B), the actual equivalent diameter decreased to less than seventy percent of the initial equivalent diameter. Again, both the decrease in size and the reduced coolant flow rate required the shutdown of the fuel cell stack for a second cleaning. The fuel cell stack was also shutdown for other reasons at 3,700 hours of operation (curve ~) -before the second cleaning. After restarting the powerplant, the equivalent diameter recovered for a short period (approximately 250 hours) before decreasing again. It is theorized that the recovery is connected with transient conditions in temperature and flow rate which occur during a shutdown and start-up of the fuel cell stack. As shown, the 3G effect is temporary.
127~8~7 The powerplant was cleaned again for a second timR. After less than sixteen hundred hours of operatlon ~curve C), the effactive diameter decreased to almost ceventy percent of the lnltlal equivalent diameter.
These periodic shutdowns and cleaning operations which result from particle deposition are both time conquming and costly.
Several approaches have been suggested for solving the problem of particle deposition from an aqueous coolant. One suggested approach is to reduce the amount of particles ~including particles that are ions) by providing a purified aqueous coolant, suppresqing corrosion by raising the coolant's p~ to high levels consistent with materials used in con~tructing the system and by reducing the dissolved oxygen levels below forty parts per billion ~40 ppb).
Chemical additives are uqed in highly contaminated solutions to promote the formation of sludge which is periodically removed from the system.
Another suggested approach for reducing the amount of particles is to use an aqueous coolant having a p~ of about 6 to 8. Moderate levels of dissolved oxygen are permitted in the water ~40-400 ppb) to suppress corrosion. Chemical additives are generally avoided.
Each of the above-mentioned methods utilizes a controlled flush rate from the system, called blowdown, which is necessary because corrosion cannot be totally eliminated and chemical cleaning is eventually required. The aqueous coolant that is lost is replaced by adding coolant. The added coolant is commonly called feedwater.
Despite the existence of these techniques for controlling the amount of iron based compounds in cooling systems having an aqueous coolant, scientists and engineers are seeking to develop additional ways of directly blocking the deposition of iron based compounds on the walls of conduits.
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Disclosure of Invention According to the present invention, an aqueous solution for use in a conduit of a fuel cell powerplant consists essentially of water that meets certain specifications and that contains an amount of ferric hydrous oxide of a character that retards the deposition of iron based compounds on the interior of tha conduit (hereinafter type II ferric hydrous oxide).
A feature of the present invention is water , having a pH which is at least 5.5, an electrical conductivity which is less than or equal to one micromho per centimeter and a solids content less than one part per million that includes an amount of iron based compounds other than type II ferric hydrous oxide. Another feature is ferric hydrous oxide disposed in the water, the ferric hydrous oxide being of a character that retards the deposition of iron based compounds on the interior of the conduit (type II ~erric hydrous oxide).
The foregoing features and advantages of the f,`., present invention will become more apparent in light of the following detailed description of the best mode for carrying out the invention and in the accompanying drawings.
Best Mode For Carrying Out The Invention Fig. 1 is a schematic representation of a fuel cell powerplant 10 which includes a fuel cell stack 12, a fuel processing system 14, a cooling system 16 and a coolant recovery an~ supply system (CRS) 18.
The cooling system lfi has a flow path 20 for coolant which, in the embodiment shown, is an aqueous solution. A means for disposing type II ferric hydrous oxide in the aqueous coolant, such as conduit 22, is in communication with the flow path 20. As shown, the conduit 22 is part of an auxiliary system 24 for supplying type II ferric hydrous oxide to the powerplant under laboratory conditions.
Alternatively, the conduit 22 might be in flow communication with the coolant recovery and supply system 18 at location 26.
The fuel cell stack 12 includes a plurality of electrochemical cells as represented by the two electrochemical cells 28. Each electrochemical cell has an anode 30, a cathode 32, and an electrolyte 34 disposed between the anode and cathode. The electrolyte places the anode in ionic communication with the cathode. Air is supplied to each cathode via conduit 36. Processed fuel is supplied to the anode via conduit 38. A portion of the fuel is combined electrochemically with a portion of the oxygen in the air via the electrolyte to produce electric power. The remaining processed fuel is exhausted from the anode and flowed via conduit 40 to 127~
the fuel processing system 14 where the fuel is combusted. The remaining oxygen is exhausted from the cathode and merged with the anode exhaust via conduit 42.
The fuel processing system 14 includes a fuel processor 44. The fuel processor receives steam via conduit 46 and a raw fuel, such as natural gas, via conduit 48. The fuel processor catalytically combines the steam and the raw fuel to produce a processed fuel such as hydrogen. Because this reaction is endothermic, the fuel processor has a burner (not shown) for generating heat. The unreacted process fuel from the stack is burned in this burner.
The cooling system has a coolant pump 50 for circulating pressurized aqueous coolant, a heat exchanger 52 for removing heat from the aqueous coolant and a steam separator 54 for separating steam from the aqueous coolant.
Under normal operating conditions, the temperature of the aqueous coolant generally reaches approximately three-hundred and fifty degrees ~ Fahrenheit (350F; 180C) and in powerplants may - typically range between 160C to 205C with an oxygen concentration ranging between 20-400 ppb with the most likely range being between 40-80ppb. Steam separated from the aqueous coolant in the steam separator 54 is flowed via conduit 46 to the fuel processor 44. Conduit 56 extends from the steam 12~
separator to the coolant pump 50 to enable the coolant pump to draw coolant from the steam separator. A blow down conduit 58 extends from conduit 56 at a point downstream of the steam separator and upstream of the coolant pump. The blow down conduit has a blow down control 60 for removing a portion of the aqueous coolant to control solids content by exhausting a portion of the coolant to exhaust conduits 40, 42.
The coolant pump 50 delivers pressurized coolant to manifold 62 via conduit 64. A plurality of conduits for the aqueous coolant, as represented by the conduits 66, extend from the manifold 62 through the fuel cell stack. These conduits are regularly spaced along the length of the fuel cell stack, as shown for example in U.S. Patent 4,233,369 issued to Breault et al. entitled "Fuel Cell Cooler Assembly and Edge Seal Means Therefor". Each conduit has an orifice 68 for controlling the distribution of coolant from the manifold to the stack. The coolant which is passed through the stack via conduit 66 is collected by manifold 70. Conduit 72 extends from ~ manifold 70 to the heat exchanger 52 to duct the - aqueous coolant to the heat exchanger where heat is removed from the coolant. Conduit 74 completes the cooling loop by extending from the heat exchanger to the steam separator 54.
The coolant recovery and supply system 18 includes a condenser 76, a degasifier 78, a boost pump 80, a water treatment system 82, and a feedwater pump 84.
1~7Q1~7 The coolant recovery and supply system 18 includes a condenser 76, a degasifier 78, a boost pump 80, a water treatment system 82, and a feedwater pump 84.
The condenser receives cathode exhaust directly from the fuel cell stack 12 via conduit 42 and combusted anode exhaust through the fuel processor 14 via conduit 40. These conduits join together with blow down conduit 58 downstream of the fuel processor 44 and duct the steam, cathode exhaust and anode exhaust to the condenser.
The condenser removes heat from the steam, the cathode exhaust and the anode exhaust. As a result, steam from the cooling system and water vapor in the anode and cathode exhaust are condensed as water.
The condensed water is flowed from the condenser via conduit 86 to the degasifier 78.
The degasifier 78 is adapted by vent 88 to receive the condensed water. The degasifier has a source of pressurized air, as represented by air pump 90, for passing air through the vent to degasify the incoming water.
The degasified water is collected below the vent at a location which is in flow communication with the boost pump 80. The boost pump 80 draws water from the degasifier via conduit 92 and supplies high pressure water through conduit 94 to the water treatment system. The water treatment system removes suspended and dissolved contaminant from the water by ~Z7UB~7 ,~
-~3-filtration and ion exchange demineralization respectively. Oxygen reduction, if desired, may be achieved by thermal steam deaeration while organic removal is achieved by absorption filtration such as commonly performed with activated charcoal. The resultant water effluent from the water treatment system is purified water. Conduit 96 extends from the water treatment system to supply purified water to the feedwater pump 84.
A recirculation conduit 98 extends to the degasifier from conduit 96 for returning a portion of the flow supplied by the boost pump to the degasifier. The recirculation conduit divides the conduit 96 into a first portion 96a in flow communication with the water treatment system and a second portion 96b in flow communication with the feedwater pump 84. The feedwater pump supplies aqueous coolant as needed to the cooling system to supply coolant as required. Conduit 100 extends from the feedwater pump through check valve 102 to the cooling system for this purpose. Conduit 100 might alternatively be in flow communication with a means for disposing type II ferric hydrous oxide in the aqueous coolant location 26.
As shown, conduit 22 is a means for disposing type II ferric hydrous oxide in the aqueous coolant and is part of the auxiliary laboratory system 24.
The auxiliary laboratory system includes a water tank 104, a water-steam deaerator 106 for storing supply :127~
l3 -~4-water (normal temperature about 212F, 100C) a heat exchanger 108 (normal temperature 140F, 60C), a boost pump 112, a water treatment system 114 tlike water treatment system 82), a feedwater pump 116 and a check valve in conduit 22 (not shown). In this particular application, the water tank and water-steam deaerator are formed as a single unit.
The auxiliary system is adapted at the following locations to receive type II ferric hydrous oxide upstream of the water treatment system at the water tank Ll or at the fill port L2; and, downstream of the water treatment system, for example, at the feedwater pump at L3.
Fig. 3 is an enlarged side elevation view of the orifice 68. The orifice has a maximum diameter Dl, a minimum diameter D2 and a contracting transition region between the maximum and minimum diameters 118.
The stippled area shows the contour of the orifice having, for example, a minimum diameter D3 which 20 might result from the accretion of particles by deposition during operation of the fuel cell powerplant. As will be realized, the deposition of a large amount of particles will increase the flow resistance of the orifice to the passage of coolant and concomitantly the flow resistance of the fuel cell stack to the coolant.
Fig. 4 is an alternate embodiment of thè fuel cell powerplant shown in Fig. 1 having means 122 for disposing ferric hydrous oxide in the coolant. The 127Q~3~7 ~5-means 122 includes means 124 for forming ferric hydrous oxide within the powerplant. The means 124 includes a tank 126, a source of process water and a source of heat. In the embodiment shown, the source of process water is the coolant recovery and supply system 18. The source of heat is the fuel cell stack 12. Means for transferring heat from the fuel cell stack to the tank, such as the cooling system 16, is in flow communication with the heated coolant via 10 conduit 128 and flow control 132. The flow control is responsive to the temperature of the aqueous solution in the tank and the blowdown requirements for the system effluent. A by-pass conduit 133 is provided to by-pass flow as required.
Fig. 5 is an enlarged, schematic representation of the means 124 for forming the hydrous ferric oxide within the power plant. The tank 126 has a first chamber 134, a second chamber 136 and a third chamber 138. The third chamber receives purified water from the water treatment system via conduit 96~. A heat exchanger 142, such as a coil of conduit 128, is disposed in the third chamber to transfer heat to the purified water and to make steam. The second and third chambers 136, 138 might be insulated against the loss of heat to the first chamber.
The second chamher 136 receives purified water via conduit 96~'and steam via conduit 144.
Alternatively, steam might be provided directly to the second chamber 136 by flowing aqueous coolant . .
127~ 7 ,~
,~
from the coolant flow path such as through conduit 128 and conduit 146 shown in phantom.
The second chamber 136 is adapted by a nozzle 148 to mix the steam from conduit 144 and the process water from conduit 96~'and inject the mixture into the chamber. One suitable nozzle for this purpose is the l/4J Siphon Spray Nozzle available from Spraying ~ystems, Inc., North Avenue, Wharton, ILL. 60187.
After injection, the water collects in the tank leaving a steam-water interface 152. The water level in chamber 136 is controlled by continuing over flow through a conduit 153 which extends back to the degasifier through conduit 98. A portion of conduit 153 is broken away for clarity. A vent 154 is provided for venting gases released during the mixing process.
The second chamber 136 has a source of iron disposed in the tank, such as rods 156 formed of an iron alloy or an iron containing liner 158 on the walls of the tank. Conduit 96a'' for withdrawing process water extends from the second chamber through the third chamber of the tank and thence to feedwater pump 84. A heat exchanger 162 is disposed in the first chamber 134. The heat exchanger is in flow communication via conduits 164a and 164b with a source of coolant, such as the purified water of conduit 96, for removing heat from the process water in conduit 96~''.
lZ7C~7 ,~
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During actual operation of the fuel cell powerplant represented in Fig. 1, the deposition of iron based compounds (that is, iron based oxides and salts including magnetite, hematite, iron phosphates and other compounds resulting from iron corrosion) is retarded by disposing in the aqueous coolant type II
ferric hydrous oxide ~that is, Fe2O3 XH2O or FeOOH
of a character that retards the deposition of iron based compounds). Experimental work has confirmed this result. A portion of this work is shown in Fig. 6.
The upper curve of Fig. 6 (curve A) is a graphical representation of the variation with time of the equivalent diameter of the fuel cell stack Dea under operative conditions. The lower curve (curve B1 beginning at about 2,000 hours shows the presence or absence of ferric hydrous oxide in the feedwater to the aqueous coolant which is supplied via auxiliary system 24 through conduit 22.
In general, Fig 6. shows that the presence of suspended type II ferric hydrous oxide in the feedwater~ as evidenced by a yellow colored feedwater filter stain reported in curve B, precedes slightly and generally corresponds to periods of stable or increasing equivalent diameter as shown by curve A.
Examples are the time periods II, IV, and VI.
Conversely, the absence of ferric hydrous oxide in the feedwater, as evidenced by the lack of a yellow - feedwater filter stain, corresponds to periods of lz7a~s ~
decreasing equivalent diameter such as periods I and V.
The effect of injecting type :tI ferric hydrous oxide is not ins-tantaneous and precedes for a short period the effect on the equivalent diameter of the fuel cell stack.
More particularly, curve A of Fig. 6 shows the equivalent diameter Dea of the fuel cell stack normalized by dividing by the initial equivalent diameter Dei. The actual equivalent diameter is Dea and is equal to Dei at the time the fuel cell stack begins operation. Curve B shows the intensity and color produced by filtering the feedwater through .45 micron filter paper in accordance with the techniques described by the Babcock and Wilcox membrane filter comparison charts. These charts are published by the Babcock and Wilcox Company, Power Generation Division, (copyright 1964, 1970) New York, New York entitled "Membrane Filter Comparison Chart (Fe2O3 . XH2O)"j "Membrane Filter Comparison Chart (Fe2O3 . XH2O-Fe3O4) l.S:l"; "Membrane Filter Comparison Char-t (Fe2O3 . XH2O-Fe3O4) 2:1";
"Membrane Filter Comparison Chart (Fe2O3 . XH2O-Fe3O4) 1:1"; and, "Membrane Filter Comparison Chart (Fe3O4)".
The comparison of the stains left by the feedwater with the membrane filter comparison chart enables an estimation of the presence of the ferric hydrous oxide in the feedwater to the cooling system.
For example, the feedwater filter stains show that 1271~7 ferric hydrous oxide was present in the feedwater in amounts of about 50 to 200 parts per billion.
Similarly, when ferric hydrous oxide was absent, black iron oxides were frequently present in an amount of about 100 to less than 10 parts per billion.
During the first 2,000 hours of operation in period I prior to the addition of type II ferric hydrous oxide, the pressure drop through the stack increased and the effective diameter decreased as iron based compounds were deposited on the walls of the cooling system.
Prior to the addition of the type II ferric hydrous oxide, the coolant for the fuel cell stack was an aqueous coolant and the feedwater was purified water from a water treatment system~ The purified water was treated condensate water fed via conduit 100 which was deionized and deoxygenated to a level of 40 to 200 parts per billion by various procedures which are well-known. This purified water will have a pH which is greater than 5.5 (preferably in a range from 5.5 - 8.0), a conductivity which is less than one micromho per centimeter, an alkalinity level of less than .2 ppm as calcium carbonate, a solids content which is less than one part per million (1 ppm) including less than 200 parts per billion of iron based compounds other than ferric hydrous oxide.
The period of time Ia shows the effect which accompanies shutdown and start-up of the powerplant ~27~
`, ~
during the period when the feedwater was only purified water. Shutdown and start-ups occurred together respectively at times Sl and S2.
Simultaneously with the start-ups, feedwater was supplied via conduit 22. Type II ferric hydrous oxide was disposed in the feedwater by injecting continuously from time Al a solution of type II
ferric hydrous oxide and purified water into the feedwater system. This feedwater solution (or feedwater) was fed through conduit 22 at a steady average flow rate of one-tenth of a gallon per minute (.1 gpm) into the flow path 20 for the aqueous coolant having a steady state average flow rate of five gallons per minute (5 gpm).
At time Al, the feedwater was flowed to the water tank at Ll upstream of the water treatment system 114. It is believed that the water treatment system removed the ferric hydrous oxide from the aqueous coolant. This is evidenced (curve B) by the absence of the yellow feedwater filter stain. As a result of the absence of ferric hydrous oxide, the equivalent diameter decreased except for the temporary effect of shutdown and start-up.
Just before the beginning of time period II at time A2, the supply of water containing type II
ferric hydrous oxide was injected into the feedwater downstream of the water treatment system at location L3, and, the water treatment system was made inactiveO The feedwater yellow filter stain reappeared and the equivalent diameter began to recover.
'1 During period II, beginning at A3, the point of injection for the ferric hydrous oxide was moved from downstream of the water treatment system ~o upstream of the water treatment system at the fill port L2, and, the water treatment system was kept inactive.
The feedwater yellow stain continued and the equivalent diameter remained stable.
During period III beginning at A4, ferric hydrous oxide was still added at location L2 upstream of the water treatment system, but the water treatment system was made active for a short period of time.
Soon after the the water treatment system was made active, the ferric hydrous oxide disappeared fron. the feedwater as evidenced by the absence of the feedwater yellow filter stain.
At time A5 at the beginning of period IV, the point of injection was moved further upstream of the water treatment system to the tank Ll, and the water treatment system was made inactive. The feedwater yellow filter stain reappeared for all of period IV.
At time A6 at the beginning of period V, injection continued at the water tank Ll upstream of the water treatment system, but now the water treatment system was made active. The ferric hydrous oxide again disappeared from the feedwater as evidenced by the absence of the yellow filter stain during period V. Shortly after A6, a six day shutdown was followed by a start-up S3. The effective diameter continued to increase for a short lZ7Q~'7 --2~--period afte~ the water treatment system was made active ~po$sibly because of shutdown and start-up), but the yelIow feedwater filter stain never reappeared and the equivalent diameter decreased for S the remaind~r of period V. This included time after Al when the point of injection of the type II ferric hydrous oxd~e was moved downstream to the fill port at L2 (but still upstream of the active water treatment system).
The downstream water treatment system was finally made inactive at time A8 at the beginning of the period VI. The yellow filter stain reappeared and the equival~nt diameter began to recover.
At time Ag, the powerplant went through a shutdown, s~tart-up cycle S5. During shutdown, the cooling sys~em was drained and refilled with water containing ~ype II ferric hydrous oxide. After Alo, the downstr~am water treatment system was kept inactive while water containing type II ferric hydrous oxi~e was continuously at the fill port L2.
The yellow Eeedwater filter stain continued and the equivalent ~iameter remained stable.
The downstream water treatment system was made active agai~ at All until Al5 when the water treatment system was by-passed. It is thought the water treat~ent system was ineffective during this period because it no longer removed the ferric hydrous ox~de as evidenced by the continued presence of the fee~ater yellow filter stain.
-2~-Type II ferric hydrous oxide continued to be added upstream of the water treatment system at A15 and A16 followed by replacement of water treatment system components. The new water treatment system components removed the ferric hydrous oxides as evidenced by the absence of the feedwater yellow stain.
Thus, the deposition of iron based compounds is retarded, in some cases eliminated, and in other cases reversed by injecting type II ferric hydrous oxide into the feedwater and thence into the aqueous coolant.
Subsequent tests showed that feedwater from the coolant recovery and supply system that was added at location 26 corrected the depositing characteristics of the iron-based compounds if it contained as little as one part type II ferric hydrous oxide water to three parts purified water.
The phenomena by which the retardation of the deposition of these iron based compounds occurs is not well understood. One working hypothesis is as follows. The iron based compounds are charged (experience suggests negatively charged) and surrounded by a cloud of oppositely charged ions to form an electrical double layer. Particles of type II ferric hydrous oxide react with the normally depositing iron based compounds to destabilize them by shrinking or eliminating the double layer, thus changing the level of charge on the compounds. As a ~27Q~3~7 ~3 result, the iron based compounds are coagulated or agglomerated by the ferric hydrous oxide to an extent that interferes with their deposition on the walls of the water conduit.
It is not certain whether the particles of ferric hydrous oxide of a character which retard deposition occur as an inorganic polymeric ion or as a colloidal particle. One critical parameter is believed to be the size of the particle in solution. The size of the particle in solution is related to the characteristic particle dimension Pd of the particle which is found by filtering the feedwater. The dimension Pd is expressed in units of length and is measured along a line extending between the two most widely separated points on the particle. Those ferric hydrous oxide compounds having a dimension Pd at the time of measurement which is greater than one micron are not believed effective, while those having a dimension up to about one tenth of a micron are known to be effective. In particular, it is known that a particle dimension of up to 100 angstroms is - the preferred characteristic particle dimension Pd.
These ferric hydrous oxide compounds may be made by any one of several processes. One way is to make the ferric hydrous oxide particles in suspension form in two steps. A concentrated solution of long shelf life (larger than one week~ is made at room temperature by slowly hydrolyzing iron in a 0.1 to 0.6 molar solution having a pH of abGut 1 to 2 for 1~7Q~3~!7 ~s-periods up to 3 months. Prior to use, the concentrated solution is diluted with distilled water to the degree desired to form the actually used solution of higher pH. The effective life of the diluted solution is believed to be another critical parameter. The effective life is shorter than the shelf life of the concentrated solution and is believed to not exceed one week.
EXAMPLE
Ferric hydrous oxide particles of a character that retards deposition of iron based compounds in a conduit were prepared in two steps as follows:
1. 20.2 grams of ferric nitrate Fe(NO3)3 9H2O
were dissolved in a sufficient amount of distilled water at room temperature to produce a pH of approximately 1.5. The solution was kept at room temperature for ten days prior to use to form a slowly hydrolyzed ferric nitrate solution. It is - believed this formed a suspension/solution of hydrous iron oxide FeOOH (Fe203-H2O) particles. Transmission electron diffraction spectroscopy of the residue left after evaporation of the water from a sample showed alpha-FeOOH (goethite) compounds were present in the residue. The characteristic particle dimension Pd of these goethite compounds ranged from 50 to 100 angstroms. The goethite crystals may exist in the solution also or they may form only during evaporation of the water. It is believed that if lZ7~8~
- refrigerated, this solution can be stored for a long period of time (at least two months).
2. The second step takes place prior to use.
Prior to testing, the pH of the concentrated solution made by step 1 was raised to about 3.5 to 4.0 by diluting the concentrated solution with distilled water. It is believed that the diluted solution at this pH is slightly unstable and deteriorates after storage for five or six days. It is believed that the size of the FeOOH particles increases with time and that after five to six days the size of the particles has increased to a size which renders the particles ineffective for the purposes of this invention.
The dilute solution was tested in an apparatus as described above. The effectiveness of the fresh, dilute solution (less than one week old) was demonstrated by reversing in fifty hours at lea.st one half the decrease in equivalent diameter of a fuel cell stack that occurred during one hundred fifty hours of operation. The equivalent diameter was then held constant for a further period of one hundred fifty hours. It is believed that this suspension/solution is effective for use in purified water as set forth above having a pH which is greater than 5.5. Water at a pH below 5.5 is not believed desirable for cooling systems for such powerplants because of the increase in corrosion of the powerplant and the possible effect that it has on the effectiveness of the ferric hydrous oxide.
~ ..
~Z7Q89~
Another method for preparing ferric hydrous oxide may be used in conjunction with the apparatus shown in Fig. 4 and Fig. 5. During operation of this embodiment, heat is transferred from the a~ueous coolant in conduit 128 to purified water in the third chamber 138 to raise steam. The steam is flowed via conduit 144 to the spray nozzle 148. Purified water is flowed via conduit 96~' to the spray nozzle from the water treatment system. The purified water has a conductivity of less than one micromho or microsiemen per centimeter (and in the embodiment shown will likely be less than 0.5 micromhos or microsiemens per centimeter), has a pH that is nearly neutral (5.5 -8), has some dissolved carbon dioxide and has an oxygen concentration of approximately 7 parts per million. In addition, the water contains iron based compounds typically in an amount of about R0-100 parts per billion.
Dissolved iron tpredominantly Fe++) is also present in the purified water supplied to the second chamber because of corrosion in the coolant recovery and supply system 18 and is present in the water contained in the bottom of the second chamber 136 because of corrosion of the iron rods 156 and the iron containing liner 158.
The steam and purified water are turbulently mixed as a result of passing through the spray nozzle 148 and are sprayed into the second chamber 136 toward the surface of the water. The second chamber 127~ 7 .il -~8-is operated at atmospheric pressure and the water in the chamber is at a temperature which promotes the formation of type II ferric hydrous oxide. In the embodiment shown, the water is at a temperature of about 212F. It is believed the temperature of the water should be in a range of about 180F to about 250F.
As the mixture is sprayed into the second chamber, portions of dissolved oxygen and carbon dioxide are released above the steam-water interface 152. These gases are vented via vent 154. Because the second chamber is vented, the bottom of the tank has a low oxygen level and a pH that promotes the type of iron corrosion that forms ferrous ions.
These ions are thought to migrate toward the steam-water interface.
Releasing portions of the dissolved carbon dioxide from the water sprayed into the second chamber and venting the carbon dioxide through vent - 20 154 has a second, important benefit. Releasing the carbon dioxide causes the pH of the water in the spray and in the tank at the surface of the water to increase slightly. The increase in pH forces dissolved iron from the water entering with the spray and possibly forces dissolved iron from the water at the steam-water interface to precipitate in the form of type II ferric hydrous oxide. It is thought this action is promoted by agitation of the iron contained in the water through the turbulent injection of the ~Z~(~85~'7 ,~9 steam and water spray. The oxygen content of the incoming water is also controlled by venting to avoid having too much oxygen present. If too much oxygen is present, the oxidation rate and subsequent precipitation is too rapid and has the undesirable result of forming Fe203 instead of forming type II
ferric hydrous oxide which is a desirable result.
After forming the water containing the type II
ferric hydrous oxide (FeOOH or Fe203-H20 of a character that retards deposition)l the water is cooled to a temperature of about 140F in a low oxygen atmosphere (less than 60 parts per billion) and is then ready for use as feedwater in the powerplant.
Water containing type II ferric hydrous oxide which is not used during the lifetime of the prepared solution returns via a recirculation conduit 98 to the degasifier tank. The water is pumped through the water treatment system bed to remove aged and ineffective ferric hydrous oxide and other compounds from the water and to supply additional purified water to the apparatus shown in Fig. 5.
The ferric hydrous oxide additive is supplied to the coolant loop through the feedwater pump as needed to replace at least a portion of the water removed from the cooling sytem and water used to make steam for the fuel processor 44. Aqueous coolant removed via the blow down control is flowed to the ferric hydrous oxide generator for heat and thence to the condenser where the water is recovered and sent to the degasifier.
~27~
"
The method of determining the freshness and characteristic particle dimension associated with the retardation in deposition includes the steps of:
1. Setting up an apparatus which accurately simulates the system having a problem with the deposition of iron based compounds.
2. Filling the cooling system with purified water.
3. Establishing the initial equivalent diameter of the system.
De = Effective Diameter, inches;
W = Total Coolant Flow (pound per hour);
d = Coolant Density (pounds per cubic foot);
N = Number of Conduits in Cell Stack;
~P = Differential Coolant Pressure Across Cell Stack (pounds per square inch, difference) ~27~8~7 Fig. 2 is an example of the effect such depositions can have on the equiv~lent diameter of a fuel cell stack under actual operative conditions.
After twenty-five hundred hours of operation (curve A) the actual equivalent diameter Dea was less then seventy percent of the initial equivalent diameter Dei. The decrease in size and the resulting decrease in the flow rate of coolant required a shutdown of the fuel cell stack for cleaning.
The fuel cell stack was cleaned after this period of operation by flowlng a pressurized, acidic solution through the conduits. Cleaning restored the actual equivalent diameter Dea to ninety-five percent of the initial effective diameter Dei (curve B).
After another twenty-two hundred hours of operation (curve B), the actual equivalent diameter decreased to less than seventy percent of the initial equivalent diameter. Again, both the decrease in size and the reduced coolant flow rate required the shutdown of the fuel cell stack for a second cleaning. The fuel cell stack was also shutdown for other reasons at 3,700 hours of operation (curve ~) -before the second cleaning. After restarting the powerplant, the equivalent diameter recovered for a short period (approximately 250 hours) before decreasing again. It is theorized that the recovery is connected with transient conditions in temperature and flow rate which occur during a shutdown and start-up of the fuel cell stack. As shown, the 3G effect is temporary.
127~8~7 The powerplant was cleaned again for a second timR. After less than sixteen hundred hours of operatlon ~curve C), the effactive diameter decreased to almost ceventy percent of the lnltlal equivalent diameter.
These periodic shutdowns and cleaning operations which result from particle deposition are both time conquming and costly.
Several approaches have been suggested for solving the problem of particle deposition from an aqueous coolant. One suggested approach is to reduce the amount of particles ~including particles that are ions) by providing a purified aqueous coolant, suppresqing corrosion by raising the coolant's p~ to high levels consistent with materials used in con~tructing the system and by reducing the dissolved oxygen levels below forty parts per billion ~40 ppb).
Chemical additives are uqed in highly contaminated solutions to promote the formation of sludge which is periodically removed from the system.
Another suggested approach for reducing the amount of particles is to use an aqueous coolant having a p~ of about 6 to 8. Moderate levels of dissolved oxygen are permitted in the water ~40-400 ppb) to suppress corrosion. Chemical additives are generally avoided.
Each of the above-mentioned methods utilizes a controlled flush rate from the system, called blowdown, which is necessary because corrosion cannot be totally eliminated and chemical cleaning is eventually required. The aqueous coolant that is lost is replaced by adding coolant. The added coolant is commonly called feedwater.
Despite the existence of these techniques for controlling the amount of iron based compounds in cooling systems having an aqueous coolant, scientists and engineers are seeking to develop additional ways of directly blocking the deposition of iron based compounds on the walls of conduits.
'~ , 127Q~39'i~
Disclosure of Invention According to the present invention, an aqueous solution for use in a conduit of a fuel cell powerplant consists essentially of water that meets certain specifications and that contains an amount of ferric hydrous oxide of a character that retards the deposition of iron based compounds on the interior of tha conduit (hereinafter type II ferric hydrous oxide).
A feature of the present invention is water , having a pH which is at least 5.5, an electrical conductivity which is less than or equal to one micromho per centimeter and a solids content less than one part per million that includes an amount of iron based compounds other than type II ferric hydrous oxide. Another feature is ferric hydrous oxide disposed in the water, the ferric hydrous oxide being of a character that retards the deposition of iron based compounds on the interior of the conduit (type II ~erric hydrous oxide).
The foregoing features and advantages of the f,`., present invention will become more apparent in light of the following detailed description of the best mode for carrying out the invention and in the accompanying drawings.
Best Mode For Carrying Out The Invention Fig. 1 is a schematic representation of a fuel cell powerplant 10 which includes a fuel cell stack 12, a fuel processing system 14, a cooling system 16 and a coolant recovery an~ supply system (CRS) 18.
The cooling system lfi has a flow path 20 for coolant which, in the embodiment shown, is an aqueous solution. A means for disposing type II ferric hydrous oxide in the aqueous coolant, such as conduit 22, is in communication with the flow path 20. As shown, the conduit 22 is part of an auxiliary system 24 for supplying type II ferric hydrous oxide to the powerplant under laboratory conditions.
Alternatively, the conduit 22 might be in flow communication with the coolant recovery and supply system 18 at location 26.
The fuel cell stack 12 includes a plurality of electrochemical cells as represented by the two electrochemical cells 28. Each electrochemical cell has an anode 30, a cathode 32, and an electrolyte 34 disposed between the anode and cathode. The electrolyte places the anode in ionic communication with the cathode. Air is supplied to each cathode via conduit 36. Processed fuel is supplied to the anode via conduit 38. A portion of the fuel is combined electrochemically with a portion of the oxygen in the air via the electrolyte to produce electric power. The remaining processed fuel is exhausted from the anode and flowed via conduit 40 to 127~
the fuel processing system 14 where the fuel is combusted. The remaining oxygen is exhausted from the cathode and merged with the anode exhaust via conduit 42.
The fuel processing system 14 includes a fuel processor 44. The fuel processor receives steam via conduit 46 and a raw fuel, such as natural gas, via conduit 48. The fuel processor catalytically combines the steam and the raw fuel to produce a processed fuel such as hydrogen. Because this reaction is endothermic, the fuel processor has a burner (not shown) for generating heat. The unreacted process fuel from the stack is burned in this burner.
The cooling system has a coolant pump 50 for circulating pressurized aqueous coolant, a heat exchanger 52 for removing heat from the aqueous coolant and a steam separator 54 for separating steam from the aqueous coolant.
Under normal operating conditions, the temperature of the aqueous coolant generally reaches approximately three-hundred and fifty degrees ~ Fahrenheit (350F; 180C) and in powerplants may - typically range between 160C to 205C with an oxygen concentration ranging between 20-400 ppb with the most likely range being between 40-80ppb. Steam separated from the aqueous coolant in the steam separator 54 is flowed via conduit 46 to the fuel processor 44. Conduit 56 extends from the steam 12~
separator to the coolant pump 50 to enable the coolant pump to draw coolant from the steam separator. A blow down conduit 58 extends from conduit 56 at a point downstream of the steam separator and upstream of the coolant pump. The blow down conduit has a blow down control 60 for removing a portion of the aqueous coolant to control solids content by exhausting a portion of the coolant to exhaust conduits 40, 42.
The coolant pump 50 delivers pressurized coolant to manifold 62 via conduit 64. A plurality of conduits for the aqueous coolant, as represented by the conduits 66, extend from the manifold 62 through the fuel cell stack. These conduits are regularly spaced along the length of the fuel cell stack, as shown for example in U.S. Patent 4,233,369 issued to Breault et al. entitled "Fuel Cell Cooler Assembly and Edge Seal Means Therefor". Each conduit has an orifice 68 for controlling the distribution of coolant from the manifold to the stack. The coolant which is passed through the stack via conduit 66 is collected by manifold 70. Conduit 72 extends from ~ manifold 70 to the heat exchanger 52 to duct the - aqueous coolant to the heat exchanger where heat is removed from the coolant. Conduit 74 completes the cooling loop by extending from the heat exchanger to the steam separator 54.
The coolant recovery and supply system 18 includes a condenser 76, a degasifier 78, a boost pump 80, a water treatment system 82, and a feedwater pump 84.
1~7Q1~7 The coolant recovery and supply system 18 includes a condenser 76, a degasifier 78, a boost pump 80, a water treatment system 82, and a feedwater pump 84.
The condenser receives cathode exhaust directly from the fuel cell stack 12 via conduit 42 and combusted anode exhaust through the fuel processor 14 via conduit 40. These conduits join together with blow down conduit 58 downstream of the fuel processor 44 and duct the steam, cathode exhaust and anode exhaust to the condenser.
The condenser removes heat from the steam, the cathode exhaust and the anode exhaust. As a result, steam from the cooling system and water vapor in the anode and cathode exhaust are condensed as water.
The condensed water is flowed from the condenser via conduit 86 to the degasifier 78.
The degasifier 78 is adapted by vent 88 to receive the condensed water. The degasifier has a source of pressurized air, as represented by air pump 90, for passing air through the vent to degasify the incoming water.
The degasified water is collected below the vent at a location which is in flow communication with the boost pump 80. The boost pump 80 draws water from the degasifier via conduit 92 and supplies high pressure water through conduit 94 to the water treatment system. The water treatment system removes suspended and dissolved contaminant from the water by ~Z7UB~7 ,~
-~3-filtration and ion exchange demineralization respectively. Oxygen reduction, if desired, may be achieved by thermal steam deaeration while organic removal is achieved by absorption filtration such as commonly performed with activated charcoal. The resultant water effluent from the water treatment system is purified water. Conduit 96 extends from the water treatment system to supply purified water to the feedwater pump 84.
A recirculation conduit 98 extends to the degasifier from conduit 96 for returning a portion of the flow supplied by the boost pump to the degasifier. The recirculation conduit divides the conduit 96 into a first portion 96a in flow communication with the water treatment system and a second portion 96b in flow communication with the feedwater pump 84. The feedwater pump supplies aqueous coolant as needed to the cooling system to supply coolant as required. Conduit 100 extends from the feedwater pump through check valve 102 to the cooling system for this purpose. Conduit 100 might alternatively be in flow communication with a means for disposing type II ferric hydrous oxide in the aqueous coolant location 26.
As shown, conduit 22 is a means for disposing type II ferric hydrous oxide in the aqueous coolant and is part of the auxiliary laboratory system 24.
The auxiliary laboratory system includes a water tank 104, a water-steam deaerator 106 for storing supply :127~
l3 -~4-water (normal temperature about 212F, 100C) a heat exchanger 108 (normal temperature 140F, 60C), a boost pump 112, a water treatment system 114 tlike water treatment system 82), a feedwater pump 116 and a check valve in conduit 22 (not shown). In this particular application, the water tank and water-steam deaerator are formed as a single unit.
The auxiliary system is adapted at the following locations to receive type II ferric hydrous oxide upstream of the water treatment system at the water tank Ll or at the fill port L2; and, downstream of the water treatment system, for example, at the feedwater pump at L3.
Fig. 3 is an enlarged side elevation view of the orifice 68. The orifice has a maximum diameter Dl, a minimum diameter D2 and a contracting transition region between the maximum and minimum diameters 118.
The stippled area shows the contour of the orifice having, for example, a minimum diameter D3 which 20 might result from the accretion of particles by deposition during operation of the fuel cell powerplant. As will be realized, the deposition of a large amount of particles will increase the flow resistance of the orifice to the passage of coolant and concomitantly the flow resistance of the fuel cell stack to the coolant.
Fig. 4 is an alternate embodiment of thè fuel cell powerplant shown in Fig. 1 having means 122 for disposing ferric hydrous oxide in the coolant. The 127Q~3~7 ~5-means 122 includes means 124 for forming ferric hydrous oxide within the powerplant. The means 124 includes a tank 126, a source of process water and a source of heat. In the embodiment shown, the source of process water is the coolant recovery and supply system 18. The source of heat is the fuel cell stack 12. Means for transferring heat from the fuel cell stack to the tank, such as the cooling system 16, is in flow communication with the heated coolant via 10 conduit 128 and flow control 132. The flow control is responsive to the temperature of the aqueous solution in the tank and the blowdown requirements for the system effluent. A by-pass conduit 133 is provided to by-pass flow as required.
Fig. 5 is an enlarged, schematic representation of the means 124 for forming the hydrous ferric oxide within the power plant. The tank 126 has a first chamber 134, a second chamber 136 and a third chamber 138. The third chamber receives purified water from the water treatment system via conduit 96~. A heat exchanger 142, such as a coil of conduit 128, is disposed in the third chamber to transfer heat to the purified water and to make steam. The second and third chambers 136, 138 might be insulated against the loss of heat to the first chamber.
The second chamher 136 receives purified water via conduit 96~'and steam via conduit 144.
Alternatively, steam might be provided directly to the second chamber 136 by flowing aqueous coolant . .
127~ 7 ,~
,~
from the coolant flow path such as through conduit 128 and conduit 146 shown in phantom.
The second chamber 136 is adapted by a nozzle 148 to mix the steam from conduit 144 and the process water from conduit 96~'and inject the mixture into the chamber. One suitable nozzle for this purpose is the l/4J Siphon Spray Nozzle available from Spraying ~ystems, Inc., North Avenue, Wharton, ILL. 60187.
After injection, the water collects in the tank leaving a steam-water interface 152. The water level in chamber 136 is controlled by continuing over flow through a conduit 153 which extends back to the degasifier through conduit 98. A portion of conduit 153 is broken away for clarity. A vent 154 is provided for venting gases released during the mixing process.
The second chamber 136 has a source of iron disposed in the tank, such as rods 156 formed of an iron alloy or an iron containing liner 158 on the walls of the tank. Conduit 96a'' for withdrawing process water extends from the second chamber through the third chamber of the tank and thence to feedwater pump 84. A heat exchanger 162 is disposed in the first chamber 134. The heat exchanger is in flow communication via conduits 164a and 164b with a source of coolant, such as the purified water of conduit 96, for removing heat from the process water in conduit 96~''.
lZ7C~7 ,~
,.. .
During actual operation of the fuel cell powerplant represented in Fig. 1, the deposition of iron based compounds (that is, iron based oxides and salts including magnetite, hematite, iron phosphates and other compounds resulting from iron corrosion) is retarded by disposing in the aqueous coolant type II
ferric hydrous oxide ~that is, Fe2O3 XH2O or FeOOH
of a character that retards the deposition of iron based compounds). Experimental work has confirmed this result. A portion of this work is shown in Fig. 6.
The upper curve of Fig. 6 (curve A) is a graphical representation of the variation with time of the equivalent diameter of the fuel cell stack Dea under operative conditions. The lower curve (curve B1 beginning at about 2,000 hours shows the presence or absence of ferric hydrous oxide in the feedwater to the aqueous coolant which is supplied via auxiliary system 24 through conduit 22.
In general, Fig 6. shows that the presence of suspended type II ferric hydrous oxide in the feedwater~ as evidenced by a yellow colored feedwater filter stain reported in curve B, precedes slightly and generally corresponds to periods of stable or increasing equivalent diameter as shown by curve A.
Examples are the time periods II, IV, and VI.
Conversely, the absence of ferric hydrous oxide in the feedwater, as evidenced by the lack of a yellow - feedwater filter stain, corresponds to periods of lz7a~s ~
decreasing equivalent diameter such as periods I and V.
The effect of injecting type :tI ferric hydrous oxide is not ins-tantaneous and precedes for a short period the effect on the equivalent diameter of the fuel cell stack.
More particularly, curve A of Fig. 6 shows the equivalent diameter Dea of the fuel cell stack normalized by dividing by the initial equivalent diameter Dei. The actual equivalent diameter is Dea and is equal to Dei at the time the fuel cell stack begins operation. Curve B shows the intensity and color produced by filtering the feedwater through .45 micron filter paper in accordance with the techniques described by the Babcock and Wilcox membrane filter comparison charts. These charts are published by the Babcock and Wilcox Company, Power Generation Division, (copyright 1964, 1970) New York, New York entitled "Membrane Filter Comparison Chart (Fe2O3 . XH2O)"j "Membrane Filter Comparison Chart (Fe2O3 . XH2O-Fe3O4) l.S:l"; "Membrane Filter Comparison Char-t (Fe2O3 . XH2O-Fe3O4) 2:1";
"Membrane Filter Comparison Chart (Fe2O3 . XH2O-Fe3O4) 1:1"; and, "Membrane Filter Comparison Chart (Fe3O4)".
The comparison of the stains left by the feedwater with the membrane filter comparison chart enables an estimation of the presence of the ferric hydrous oxide in the feedwater to the cooling system.
For example, the feedwater filter stains show that 1271~7 ferric hydrous oxide was present in the feedwater in amounts of about 50 to 200 parts per billion.
Similarly, when ferric hydrous oxide was absent, black iron oxides were frequently present in an amount of about 100 to less than 10 parts per billion.
During the first 2,000 hours of operation in period I prior to the addition of type II ferric hydrous oxide, the pressure drop through the stack increased and the effective diameter decreased as iron based compounds were deposited on the walls of the cooling system.
Prior to the addition of the type II ferric hydrous oxide, the coolant for the fuel cell stack was an aqueous coolant and the feedwater was purified water from a water treatment system~ The purified water was treated condensate water fed via conduit 100 which was deionized and deoxygenated to a level of 40 to 200 parts per billion by various procedures which are well-known. This purified water will have a pH which is greater than 5.5 (preferably in a range from 5.5 - 8.0), a conductivity which is less than one micromho per centimeter, an alkalinity level of less than .2 ppm as calcium carbonate, a solids content which is less than one part per million (1 ppm) including less than 200 parts per billion of iron based compounds other than ferric hydrous oxide.
The period of time Ia shows the effect which accompanies shutdown and start-up of the powerplant ~27~
`, ~
during the period when the feedwater was only purified water. Shutdown and start-ups occurred together respectively at times Sl and S2.
Simultaneously with the start-ups, feedwater was supplied via conduit 22. Type II ferric hydrous oxide was disposed in the feedwater by injecting continuously from time Al a solution of type II
ferric hydrous oxide and purified water into the feedwater system. This feedwater solution (or feedwater) was fed through conduit 22 at a steady average flow rate of one-tenth of a gallon per minute (.1 gpm) into the flow path 20 for the aqueous coolant having a steady state average flow rate of five gallons per minute (5 gpm).
At time Al, the feedwater was flowed to the water tank at Ll upstream of the water treatment system 114. It is believed that the water treatment system removed the ferric hydrous oxide from the aqueous coolant. This is evidenced (curve B) by the absence of the yellow feedwater filter stain. As a result of the absence of ferric hydrous oxide, the equivalent diameter decreased except for the temporary effect of shutdown and start-up.
Just before the beginning of time period II at time A2, the supply of water containing type II
ferric hydrous oxide was injected into the feedwater downstream of the water treatment system at location L3, and, the water treatment system was made inactiveO The feedwater yellow filter stain reappeared and the equivalent diameter began to recover.
'1 During period II, beginning at A3, the point of injection for the ferric hydrous oxide was moved from downstream of the water treatment system ~o upstream of the water treatment system at the fill port L2, and, the water treatment system was kept inactive.
The feedwater yellow stain continued and the equivalent diameter remained stable.
During period III beginning at A4, ferric hydrous oxide was still added at location L2 upstream of the water treatment system, but the water treatment system was made active for a short period of time.
Soon after the the water treatment system was made active, the ferric hydrous oxide disappeared fron. the feedwater as evidenced by the absence of the feedwater yellow filter stain.
At time A5 at the beginning of period IV, the point of injection was moved further upstream of the water treatment system to the tank Ll, and the water treatment system was made inactive. The feedwater yellow filter stain reappeared for all of period IV.
At time A6 at the beginning of period V, injection continued at the water tank Ll upstream of the water treatment system, but now the water treatment system was made active. The ferric hydrous oxide again disappeared from the feedwater as evidenced by the absence of the yellow filter stain during period V. Shortly after A6, a six day shutdown was followed by a start-up S3. The effective diameter continued to increase for a short lZ7Q~'7 --2~--period afte~ the water treatment system was made active ~po$sibly because of shutdown and start-up), but the yelIow feedwater filter stain never reappeared and the equivalent diameter decreased for S the remaind~r of period V. This included time after Al when the point of injection of the type II ferric hydrous oxd~e was moved downstream to the fill port at L2 (but still upstream of the active water treatment system).
The downstream water treatment system was finally made inactive at time A8 at the beginning of the period VI. The yellow filter stain reappeared and the equival~nt diameter began to recover.
At time Ag, the powerplant went through a shutdown, s~tart-up cycle S5. During shutdown, the cooling sys~em was drained and refilled with water containing ~ype II ferric hydrous oxide. After Alo, the downstr~am water treatment system was kept inactive while water containing type II ferric hydrous oxi~e was continuously at the fill port L2.
The yellow Eeedwater filter stain continued and the equivalent ~iameter remained stable.
The downstream water treatment system was made active agai~ at All until Al5 when the water treatment system was by-passed. It is thought the water treat~ent system was ineffective during this period because it no longer removed the ferric hydrous ox~de as evidenced by the continued presence of the fee~ater yellow filter stain.
-2~-Type II ferric hydrous oxide continued to be added upstream of the water treatment system at A15 and A16 followed by replacement of water treatment system components. The new water treatment system components removed the ferric hydrous oxides as evidenced by the absence of the feedwater yellow stain.
Thus, the deposition of iron based compounds is retarded, in some cases eliminated, and in other cases reversed by injecting type II ferric hydrous oxide into the feedwater and thence into the aqueous coolant.
Subsequent tests showed that feedwater from the coolant recovery and supply system that was added at location 26 corrected the depositing characteristics of the iron-based compounds if it contained as little as one part type II ferric hydrous oxide water to three parts purified water.
The phenomena by which the retardation of the deposition of these iron based compounds occurs is not well understood. One working hypothesis is as follows. The iron based compounds are charged (experience suggests negatively charged) and surrounded by a cloud of oppositely charged ions to form an electrical double layer. Particles of type II ferric hydrous oxide react with the normally depositing iron based compounds to destabilize them by shrinking or eliminating the double layer, thus changing the level of charge on the compounds. As a ~27Q~3~7 ~3 result, the iron based compounds are coagulated or agglomerated by the ferric hydrous oxide to an extent that interferes with their deposition on the walls of the water conduit.
It is not certain whether the particles of ferric hydrous oxide of a character which retard deposition occur as an inorganic polymeric ion or as a colloidal particle. One critical parameter is believed to be the size of the particle in solution. The size of the particle in solution is related to the characteristic particle dimension Pd of the particle which is found by filtering the feedwater. The dimension Pd is expressed in units of length and is measured along a line extending between the two most widely separated points on the particle. Those ferric hydrous oxide compounds having a dimension Pd at the time of measurement which is greater than one micron are not believed effective, while those having a dimension up to about one tenth of a micron are known to be effective. In particular, it is known that a particle dimension of up to 100 angstroms is - the preferred characteristic particle dimension Pd.
These ferric hydrous oxide compounds may be made by any one of several processes. One way is to make the ferric hydrous oxide particles in suspension form in two steps. A concentrated solution of long shelf life (larger than one week~ is made at room temperature by slowly hydrolyzing iron in a 0.1 to 0.6 molar solution having a pH of abGut 1 to 2 for 1~7Q~3~!7 ~s-periods up to 3 months. Prior to use, the concentrated solution is diluted with distilled water to the degree desired to form the actually used solution of higher pH. The effective life of the diluted solution is believed to be another critical parameter. The effective life is shorter than the shelf life of the concentrated solution and is believed to not exceed one week.
EXAMPLE
Ferric hydrous oxide particles of a character that retards deposition of iron based compounds in a conduit were prepared in two steps as follows:
1. 20.2 grams of ferric nitrate Fe(NO3)3 9H2O
were dissolved in a sufficient amount of distilled water at room temperature to produce a pH of approximately 1.5. The solution was kept at room temperature for ten days prior to use to form a slowly hydrolyzed ferric nitrate solution. It is - believed this formed a suspension/solution of hydrous iron oxide FeOOH (Fe203-H2O) particles. Transmission electron diffraction spectroscopy of the residue left after evaporation of the water from a sample showed alpha-FeOOH (goethite) compounds were present in the residue. The characteristic particle dimension Pd of these goethite compounds ranged from 50 to 100 angstroms. The goethite crystals may exist in the solution also or they may form only during evaporation of the water. It is believed that if lZ7~8~
- refrigerated, this solution can be stored for a long period of time (at least two months).
2. The second step takes place prior to use.
Prior to testing, the pH of the concentrated solution made by step 1 was raised to about 3.5 to 4.0 by diluting the concentrated solution with distilled water. It is believed that the diluted solution at this pH is slightly unstable and deteriorates after storage for five or six days. It is believed that the size of the FeOOH particles increases with time and that after five to six days the size of the particles has increased to a size which renders the particles ineffective for the purposes of this invention.
The dilute solution was tested in an apparatus as described above. The effectiveness of the fresh, dilute solution (less than one week old) was demonstrated by reversing in fifty hours at lea.st one half the decrease in equivalent diameter of a fuel cell stack that occurred during one hundred fifty hours of operation. The equivalent diameter was then held constant for a further period of one hundred fifty hours. It is believed that this suspension/solution is effective for use in purified water as set forth above having a pH which is greater than 5.5. Water at a pH below 5.5 is not believed desirable for cooling systems for such powerplants because of the increase in corrosion of the powerplant and the possible effect that it has on the effectiveness of the ferric hydrous oxide.
~ ..
~Z7Q89~
Another method for preparing ferric hydrous oxide may be used in conjunction with the apparatus shown in Fig. 4 and Fig. 5. During operation of this embodiment, heat is transferred from the a~ueous coolant in conduit 128 to purified water in the third chamber 138 to raise steam. The steam is flowed via conduit 144 to the spray nozzle 148. Purified water is flowed via conduit 96~' to the spray nozzle from the water treatment system. The purified water has a conductivity of less than one micromho or microsiemen per centimeter (and in the embodiment shown will likely be less than 0.5 micromhos or microsiemens per centimeter), has a pH that is nearly neutral (5.5 -8), has some dissolved carbon dioxide and has an oxygen concentration of approximately 7 parts per million. In addition, the water contains iron based compounds typically in an amount of about R0-100 parts per billion.
Dissolved iron tpredominantly Fe++) is also present in the purified water supplied to the second chamber because of corrosion in the coolant recovery and supply system 18 and is present in the water contained in the bottom of the second chamber 136 because of corrosion of the iron rods 156 and the iron containing liner 158.
The steam and purified water are turbulently mixed as a result of passing through the spray nozzle 148 and are sprayed into the second chamber 136 toward the surface of the water. The second chamber 127~ 7 .il -~8-is operated at atmospheric pressure and the water in the chamber is at a temperature which promotes the formation of type II ferric hydrous oxide. In the embodiment shown, the water is at a temperature of about 212F. It is believed the temperature of the water should be in a range of about 180F to about 250F.
As the mixture is sprayed into the second chamber, portions of dissolved oxygen and carbon dioxide are released above the steam-water interface 152. These gases are vented via vent 154. Because the second chamber is vented, the bottom of the tank has a low oxygen level and a pH that promotes the type of iron corrosion that forms ferrous ions.
These ions are thought to migrate toward the steam-water interface.
Releasing portions of the dissolved carbon dioxide from the water sprayed into the second chamber and venting the carbon dioxide through vent - 20 154 has a second, important benefit. Releasing the carbon dioxide causes the pH of the water in the spray and in the tank at the surface of the water to increase slightly. The increase in pH forces dissolved iron from the water entering with the spray and possibly forces dissolved iron from the water at the steam-water interface to precipitate in the form of type II ferric hydrous oxide. It is thought this action is promoted by agitation of the iron contained in the water through the turbulent injection of the ~Z~(~85~'7 ,~9 steam and water spray. The oxygen content of the incoming water is also controlled by venting to avoid having too much oxygen present. If too much oxygen is present, the oxidation rate and subsequent precipitation is too rapid and has the undesirable result of forming Fe203 instead of forming type II
ferric hydrous oxide which is a desirable result.
After forming the water containing the type II
ferric hydrous oxide (FeOOH or Fe203-H20 of a character that retards deposition)l the water is cooled to a temperature of about 140F in a low oxygen atmosphere (less than 60 parts per billion) and is then ready for use as feedwater in the powerplant.
Water containing type II ferric hydrous oxide which is not used during the lifetime of the prepared solution returns via a recirculation conduit 98 to the degasifier tank. The water is pumped through the water treatment system bed to remove aged and ineffective ferric hydrous oxide and other compounds from the water and to supply additional purified water to the apparatus shown in Fig. 5.
The ferric hydrous oxide additive is supplied to the coolant loop through the feedwater pump as needed to replace at least a portion of the water removed from the cooling sytem and water used to make steam for the fuel processor 44. Aqueous coolant removed via the blow down control is flowed to the ferric hydrous oxide generator for heat and thence to the condenser where the water is recovered and sent to the degasifier.
~27~
"
The method of determining the freshness and characteristic particle dimension associated with the retardation in deposition includes the steps of:
1. Setting up an apparatus which accurately simulates the system having a problem with the deposition of iron based compounds.
2. Filling the cooling system with purified water.
3. Establishing the initial equivalent diameter of the system.
4. Operating the cooling system: until a ten percent decrease in the effective diameter occurs;
and, until the rate of decrease is established by measuring the decrease as a function of time.
and, until the rate of decrease is established by measuring the decrease as a function of time.
5. Adding an amount of ferric hydrous oxide to the water flowed through the orifice, the residue of the ferric hydrous oxide having particles of a known characteristic particle dimension Pd.
6. Determining whether the deposition of iron based compounds has been blocked by monitoring the pressure drop and flow rate to determine whether the equivalent diameter decreases at the same rate (deposition not halted), decreases at a much reduced rate (blockage of deposition) stays the same (completely blocks deposition), or increases (reversal of the deposition process). The process is repeated with ferric hydrous oxide particles in varying amounts and varying freshness having a characteristic particle dimension which is smaller and smaller in size until finally the desired effect is observed.
,.
~;~7Q~7 3~
--,3~1--Having established the effectiveness of the ferric hydrous oxide particles, the particles are added to the aqueous coolant, thus increasing the life of the cooling sytem and increasing the time between costly shutdowns and overhauls of the cooling systems.
Although the invention has been shown and described with respect to detailed embodiments thereof, it should be understood by those skilled in the art that various changes in form and detail thereof may be made without departing from the spirit and the scope of the claimed invention.
,.
~;~7Q~7 3~
--,3~1--Having established the effectiveness of the ferric hydrous oxide particles, the particles are added to the aqueous coolant, thus increasing the life of the cooling sytem and increasing the time between costly shutdowns and overhauls of the cooling systems.
Although the invention has been shown and described with respect to detailed embodiments thereof, it should be understood by those skilled in the art that various changes in form and detail thereof may be made without departing from the spirit and the scope of the claimed invention.
Claims (8)
1. A fuel cell powerplant having a fuel cell stack, a flow path for an aqueous solution, a conduit for the aqueous solution through which the flow path extends, and a component for transferring heat to the aqueous solution, the aqueous solution including water and iron based compounds which deposit on the interior of the conduit, the water being capable of reacting with its environment to form iron based compounds, wherein the improvement comprises:
an aqueous solution consisting essentially of water having a pH of about 5.5 to 8.5, having an electrical conductivity which is less than or equal to one micromho per centimeter, having a solids content which is less than one part per million (1 ppm), the solids content including an amount of iron based compounds other than ferric hydrous oxide and the water further containing ferric hydrous oxide of a character that retards the deposition of said iron based compounds on the interior of the conduit; and, means for disposing additional ferric hydrous oxide in the aqueous solution of a character that retards the deposition of said iron based compounds on the interior of the conduit which includes means for forming the additional ferric hydrous oxide by the controlled corrosion of iron or an iron based compound, the means being disposed within the powerplant and receiving water from a conduit in flow communication with a component of the fuel cell powerplant.
an aqueous solution consisting essentially of water having a pH of about 5.5 to 8.5, having an electrical conductivity which is less than or equal to one micromho per centimeter, having a solids content which is less than one part per million (1 ppm), the solids content including an amount of iron based compounds other than ferric hydrous oxide and the water further containing ferric hydrous oxide of a character that retards the deposition of said iron based compounds on the interior of the conduit; and, means for disposing additional ferric hydrous oxide in the aqueous solution of a character that retards the deposition of said iron based compounds on the interior of the conduit which includes means for forming the additional ferric hydrous oxide by the controlled corrosion of iron or an iron based compound, the means being disposed within the powerplant and receiving water from a conduit in flow communication with a component of the fuel cell powerplant.
2. The powerplant as claimed in claim 1 wherein said conduit is a first conduit and the powerplant further includes a second conduit for flowing at least a portion of said aqueous solution to the means for forming additional ferric hydrous oxide.
3. The powerplant as claimed in claim 2 wherein said conduit is a first conduit and the powerplant further includes a second conduit for flowing at least a portion of said aqueous solution to the means for forming additional ferric hydrous oxide to provide water for corroding the iron or iron based compound.
4. The powerplant as claimed in claim 2 wherein said conduit is a first conduit and the powerplant further includes a second conduit for flowing at least a portion of said aqueous solution to the means for forming additional ferric hydrous oxide to provide heat for raising steam.
5. The powerplant as claimed in claim 2 wherein said conduit is a first conduit and the powerplant further includes a second conduit for flowing at least a portion of said aqueous solution to the means for forming additional ferric hydrous oxide to provide steam to the means for forming additional ferric hydrous oxide.
6. The powerplant as claimed in claim 1 wherein said flow path extends through the fuel cell stack and wherein the conduit is in flow communication with a condenser for condensing water vapor contained in said flow path from the fuel cell.
7. The powerplant as claimed in claims 2, 3 or 4 wherein the powerplant has a fuel cell stack which generates heat under operative conditions and wherein the powerplant further includes means for transferring heat from the fuel cell stack to the means for forming ferric hydrous oxide in the water such that the water is heated to a temperature of approximately one hundred degrees Celsius (100°C) to raise steam.
8. The powerplant as claimed in claim 3 wherein the means for disposing ferric hydrous oxide in the water includes means for establishing a level of oxygen dissolved in the water such that the water contains oxygen in an amount of 20 to 400 parts per billion and includes a means for demineralizing the water such that the water is neutral and has an alkalinity level of less than 0.2 ppm as calcium carbonate and a solids content which is less than one part per million (1 ppm).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US746,167 | 1985-06-18 | ||
| US06/746,167 US4804591A (en) | 1985-06-18 | 1985-06-18 | Fuel cell powerplant employing an aqueous solution |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1270897A true CA1270897A (en) | 1990-06-26 |
Family
ID=24999735
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000511820A Expired - Lifetime CA1270897A (en) | 1985-06-18 | 1986-06-18 | Fuel cell powerplant employing an aqueous solution |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4804591A (en) |
| JP (1) | JPS61292861A (en) |
| CA (1) | CA1270897A (en) |
| DE (1) | DE3620330A1 (en) |
| FR (1) | FR2583582A1 (en) |
| GB (1) | GB2178221B (en) |
| NL (1) | NL8601578A (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4923767A (en) * | 1985-06-18 | 1990-05-08 | International Fuel Cells | Fuel cell power plants employing an aqueous solution |
| JP2656382B2 (en) * | 1990-05-10 | 1997-09-24 | 株式会社東芝 | Water treatment system for fuel cell power plant |
| US6126908A (en) * | 1996-08-26 | 2000-10-03 | Arthur D. Little, Inc. | Method and apparatus for converting hydrocarbon fuel into hydrogen gas and carbon dioxide |
| US6280867B1 (en) | 1997-12-05 | 2001-08-28 | Griff Consulting, Inc. | Apparatus for pumping a fluid in a fuel cell system |
| US6207308B1 (en) | 1999-04-20 | 2001-03-27 | International Fuel Cells, Llc | Water treatment system for a fuel cell assembly |
| US6641625B1 (en) | 1999-05-03 | 2003-11-04 | Nuvera Fuel Cells, Inc. | Integrated hydrocarbon reforming system and controls |
| US6242118B1 (en) | 1999-10-14 | 2001-06-05 | International Fuel Cells Llc | Method and apparatus for removing contaminants from the coolant supply of a fuel cell power plant |
| US6428916B1 (en) | 1999-12-20 | 2002-08-06 | Utc Fuel Cells, Llc | Coolant treatment system for a direct antifreeze cooled fuel cell assembly |
| US7507384B2 (en) * | 2002-06-13 | 2009-03-24 | Nuvera Fuel Cells, Inc. | Preferential oxidation reactor temperature regulation |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE526503A (en) * | ||||
| BE379015A (en) * | ||||
| FR519200A (en) * | 1920-06-10 | 1921-06-06 | Paul Kestner | Improvements to water degassing processes using metal filters |
| DE690800C (en) * | 1936-09-03 | 1940-05-08 | Ehrich & Graetz Akt Ges | Short built gas lamp |
| FR1051522A (en) * | 1951-05-07 | 1954-01-18 | G & J Weir Ltd | Seawater treatment method for evaporation plants |
| US3923546A (en) * | 1974-12-13 | 1975-12-02 | United Technologies Corp | Corrosion protection for a fuel cell coolant system |
| US4430228A (en) * | 1979-12-14 | 1984-02-07 | Paterson Laurene O | Process for removing dissolved iron from water |
| NL8120502A (en) * | 1981-01-19 | 1982-12-01 | United Technologies Corp | SYSTEM AND METHOD FOR CLEANING REFRIGERANT FOR A FUEL CELL ENERGY DEVICE. |
| US4344849A (en) * | 1981-01-19 | 1982-08-17 | United Technologies Corporation | Fuel cell power plant self-controlling coolant cleaning process |
| EP0083571B1 (en) * | 1982-01-06 | 1986-04-16 | Alcan International Limited | Method of reducing corrosion of aluminium components |
| US4835072A (en) * | 1985-06-17 | 1989-05-30 | International Fuel Cells Corporation | Apparatus employing an aqueous solution |
| US4670357A (en) * | 1985-06-17 | 1987-06-02 | International Fuel Cells Corporation | Fuel cell powerplant employing an aqueous solution |
-
1985
- 1985-06-18 US US06/746,167 patent/US4804591A/en not_active Expired - Fee Related
-
1986
- 1986-06-03 GB GB8613396A patent/GB2178221B/en not_active Expired
- 1986-06-11 JP JP61137253A patent/JPS61292861A/en active Pending
- 1986-06-18 NL NL8601578A patent/NL8601578A/en not_active Application Discontinuation
- 1986-06-18 CA CA000511820A patent/CA1270897A/en not_active Expired - Lifetime
- 1986-06-18 DE DE19863620330 patent/DE3620330A1/en not_active Withdrawn
- 1986-06-18 FR FR8608810A patent/FR2583582A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US4804591A (en) | 1989-02-14 |
| DE3620330A1 (en) | 1986-12-18 |
| GB8613396D0 (en) | 1986-07-09 |
| FR2583582A1 (en) | 1986-12-19 |
| NL8601578A (en) | 1987-01-16 |
| JPS61292861A (en) | 1986-12-23 |
| GB2178221A (en) | 1987-02-04 |
| GB2178221B (en) | 1989-02-22 |
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