The present invention relates to electrochemical devices that function by maintaining separate gaseous streams and causing reactions to occur at the surfaces of conductive layers of adjacent components.
Electrochemical devices having multiple components, such as, for example, solid oxide fuel cell (SOFC) stacks, syngas membrane reactors, oxygen generators and the like require a critical seal technology to separate gas streams (e.g., H2 and O2) and to prevent the streams from mixing with each other. Mixing of the gas streams has a variety of negative consequences, depending upon the type of device and the composition of the gaseous streams. One major problem that results from mixing of such gases is the possibility of thermal combustion of the gases and the resulting failure of the device.
One type of electrochemical device that has received, and continues to receive, significant attention is a fuel cell device. Fuel cell devices are known and used for the direct production of electricity from standard fuel materials including fossil fuels, hydrogen, and the like by converting chemical energy of a fuel directly to electrical energy. This conversion is accomplished by oxidizing the fuel without an intermediate thermal energy stage. Fuel cells typically include a porous anode, a porous cathode, and a solid or liquid electrolyte therebetween. Fuel (e.g., hydrogen) is fed to the anode where it is oxidized and electrons are released to the external circuit. Oxidant (e.g., oxygen) is fed to the cathode where it is reduced and electrons are accepted from the external circuit. The electron flow through the external circuit produces direct-current electricity. The electrolyte conducts ions between the two electrodes.
Fuel cells are classified into several types according to the electrolyte used to accommodate ion transfer during operation. Examples of electrolytes include aqueous potassium hydroxide, concentrated phosphoric acid, fused alkali carbonate, solid polymers, e.g., a solid polymer ion exchange membrane, and solid oxides, e.g., a stabilized zirconium oxide. Solid oxide fuel cell (“SOFC”) devices have attracted considerable attention as the fuel cells of the third generation following phosphoric acid fuel cells and molten carbonate fuel cells of the first and second generations, respectively. SOFC devices have an advantage in enhancing efficiency of generation of electricity, including waste heat management, with their operation at high temperatures, typically above about 650° C.
Those involved in research and development of SOFC technology consider SOFC power generation as an emerging viable alternative to the use of internal combustion engines. Contrary to internal combustion, the oxygen is transported in a SOFC device via the vacancy mechanism through a dense ceramic electrolyte, and then reacted with the hydrogen electrochemically. Because the SOFC converts the chemical energy to electrical energy without the intermediate thermal energy step, its conversion efficiency is not subject to the Carnot Limit. Compared to conventional power generation, SOFC technology offers several advantages, including, for example, substantially higher efficiency, modular construction, minimal site restriction, and much lower air pollution.
In a typical SOFC, a solid electrolyte, made of dense yttria-stabllized zirconia (YSZ) ceramic, separates a porous ceramic anode from a porous ceramic cathode. The anode typically is made of nickel/YSZ cermet, and the cathode is typically made of doped lanthanum manganite. In such a fuel cell, an example of which is shown schematically in
When fuel is supplied to the anode and oxidant is supplied to the cathode, a useable electric current is electrochemically generated by the flow of electrons through the external circuit from the anode to the cathode. As an example, the chemical reaction for a fuel cell using hydrogen as the fuel and oxygen as the oxidant is shown in equation (1).
H2+½O2→H2O (Eq. 1)
This process occurs through two redox or separate half-reactions which occur at the electrodes as follows:
Anode Reaction
H2+O2−→H2O+2e− (Eq. 2)
Cathode Reaction
½O2+2e−→O2− (Eq. 3)
In the anode half-reaction, the hydrogen fuel is oxidized by oxygen ions from the electrolyte, thereby releasing electrons (e−) to the external circuit as shown in equation (2) and as shown schematically in
Because each individual electrochemical cell, made of a single anode, a single electrolyte, and a single cathode, generates an open circuit voltage of about one volt, and each cell is subject to electrode activation polarization losses, electrical resistance losses, and ion mobility resistant losses which reduce its output to even lower voltages at a useful current, a fuel cell assembly comprising a plurality of fuel cell units electrically connected to each other is required to produce the desired voltage or current to generate commercially useful quantities of power.
Currently, there are two basic designs for SOFC applications: tubular and planar. With respect to planar SOFC designs, the individual electrochemical cells are typically connected together in series to form a stack. For example, planar solid oxide fuel cell stacks typically comprise a plurality of stacked cathode-electrolyte-anode-interconnect repeat units, and the fuel cell stack includes an electrical interconnect between the cathode and the anode of adjacent cells. The fuel cell assembly also includes ducts or manifolding to conduct the fuel and oxidant into and out of the stack. Channels for gas flow, either in a cross-flow or a co-flow or a counterflow configuration, are usually incorporated into the cathode, anode and/or interconnect. Planar designs are believed to potentially offer lower cost and higher power density per unit volume compared to tubular designs; however, planar designs face many challenges that must be overcome.
In addition to the challenges in materials development for electrolytes, anodes, and cathodes, planar SOFC designs require seals between each individual cell to prevent (or at least sufficiently minimize) leaking of gases from the stack as well as mixing of fuel and oxidant gases. Low fuel leak rates are required if SOFC stacks are to operate safely and economically. Furthermore, the seal needs to have long-term stability at the elevated temperatures and harsh (oxidizing, reducing and humid) environments typical of SOFCs during operation. Also, the seals should not cause corrosion or other degradation of the materials with which they are in contact (e.g., stabilized zirconia, interconnect, and electrodes). Perhaps most significantly, the seal needs to be suitably durable to acceptably perform its sealing function under repetitive thermal cycling.
A variety of features of a SOFC stack add to the difficulty of obtaining a good seal. For one, both the cell (including anode, electrolyte and cathode layers) and the interconnect, whether of ceramic or metallic material, are rigid. As a result, to achieve an effective seal, the mating surfaces between the cell and the interconnect must be flat and parallel. Nevertheless, because all of the components are rigid, even with good flatness, it is necessary to seal the surfaces in some manner to prevent leakage of the gases.
Another feature of electrochemical devices, such as SOFCs, that lends to the difficulty of obtaining a good seal relates to the fact that diverse compositions are used as the components of a SOFC device, and the diverse compositions have differing thermal expansion characteristics. In this regard, in various types of fuel cell assemblies adapted for use at high operating temperatures, a monolithic design is used in which the entire structure is made of ceramics. In other designs, individual components are rigidly and hermetically sealed using, for example, glass seals, glass-ceramic seals, cermet seals or metallic braze. While such monolithic or rigidly formed fuel cells are well equipped to prevent gas leakage, ceramics have the inherent material characteristic of low ductility and low toughness. Consequently, they are susceptible to damage by mechanical vibrations and shocks. Furthermore, and perhaps more problematic, such assemblies are extremely susceptible to thermal shocks and to thermally induced mechanical stresses due to the different thermal expansion characteristics of the components.
A wide variety of applications for which SOFC devices can be used to advantage involve intermittent power demands, and thus involve intermittent usage and nonusage, and thus repeated heating and cooling cycles. Given the variety of materials used to make a single cell, and the difficulty of selecting suitable materials that have precisely matched coefficients of thermal expansion, it is readily seen that the use of rigid seals presents significant problems. Furthermore, where the fuel cell is designed to be used at lower temperatures with a low-temperature ceramic electrolyte, some components of the fuel cell may be made of metals, which are generally less expensive to fabricate than ceramic components and have the advantage of improved ductility and fracture toughness, making them more resistant to mechanical and thermal shock damage than ceramics. However, in a fuel cell using metals for at least some components and ceramics for at least some components, rigid sealing is perhaps an even greater problem because most alloys potentially suitable for the SOFC interconnect application have much higher coefficients of thermal expansion than do ceramics, resulting in large thermal stresses and strains produced during operation of such a fuel cell. When a metal/ceramic fuel cell is heated and cooled, the dimensions of the metal components change more than the dimensions of the ceramic components, leading to thermal strains within the structure. These thermal strains produce thermal stresses that can lead to failure of the ceramic components or the rigid seals between the ceramic and metal components.
Another type of seal that has been considered for use in connection with SOFC devices is a compressive seal. In a device designed to utilize a compressive seal, a layer of inert material is placed between components of the SOFC and a compressive force is applied to the components and the material therebetween in an attempt to block leakage between the components. In comparison to rigid ceramic, glass or metallic seals, compressive seals potentially offer several advantages. Since they are not rigidly bonded to the cells, the need for matching coefficients of thermal expansion (CTE) of all stack components is reduced or eliminated. The cells and interconnects are allowed to expand and contract more freely during thermal cycling and operation, thereby reducing structural degradation during thermal cycling and routine operation. Elimination of the need for matching CTE greatly expands the list of candidate interconnect materials, whether ceramic or metallic. The compressive seals also have two unique advantages over rigid seals. One is that cells in stacks may be reusable since they are not bonded with one another. Secondly, it allows non-destructive post-service analysis
Research in the area of the compressive seals is still in its early stages and very little data is available. One group discussed the use of compressed mica in a single-cell SOFC set-up; however the effectiveness was not discussed. (Kim and Virkar, Solid Oxide Fuel Cells (SOFC VI) Proceedings of the Sixth International Symposium, edited by S. C. Sighal and M. Dokiya, The Electrochemical Society, Proceedings Volume 99-19, 830 (1999)). A recent publication discusses work relating to micas in paper form and cleaved single crystal micas as compressive seals for SOFC applications. (Simner et al. “Compressive mica seals for SOFC applications,” J. Power Sources, 102 [1-2], 310-316, (2001)). The results showed that cleaved natural mica sheets were far superior compared to mica papers. For the mica sheets, leak rates of about 0.33-0.65 sccm/cm at 800° C. and 100 psi were measured on small test coupons simulating a single interconnect/seal/cell/seal/interconnect unit. A coupon leak rate of 0.33-0.65 sccm/cm, however, is believed to translate to unacceptably high leak rates for actual SOFC stacks, in which multiple, full size components would be stacked together with the gaskets between each component.
In view of the above background, it is apparent that one important challenge in the development of SOFC assemblies and other electrochemical devices is the development of sealing technology offering suitably low leak rates. There is a continuing need for further developments in the field of seals for such electrochemical devices. The present invention addresses this need, and further provides related advantages.
Accordingly, it is one object of this invention to provide devices and methods for sealing between components of an electrochemical device, such as, for example, a solid oxide fuel cell stack, a syngas membrane reactor, an oxygen generator and the like.
It is another object of this invention to provide solid oxide fuel cell stacks and other electrochemical devices that can be subjected to wide variations in temperature without rapid failure from cracking.
It is yet another object of this invention to provide solid oxide fuel cell stacks and other electrochemical devices for which thermal expansion match between components thereof is not required.
These and other objects of this invention are achieved by the present invention, which provides electrochemical devices, such as, for example, solid oxide fuel cell devices, syngas membrane reactors, oxygen generators and the like, that include novel multi-layer seals between components to prevent intermixing of diverse gaseous streams.
The present invention also provides solid oxide fuel cell stacks and other electrochemical devices that can be subjected to wide variations in temperature without rapid failure from cracking.
The present invention also provides solid oxide fuel cell stacks and other electrochemical devices for which thermal expansion match between components thereof is not required.
The present invention also provides novel multi-layer compressive seals that provide excellent leak barriers at high temperatures, and methods for making and using same.
Further forms, embodiments, objects, features, and aspects of the present invention shall become apparent from the description contained herein.
Although the characteristic features of this invention will be particularly pointed out in the claims, the invention itself, and the manner in which it may be made and used, may be better understood by referring to the following description taken in connection with the accompanying figures forming a part hereof.
For the purpose of promoting an understanding of the principles of the invention, reference will now be made to preferred embodiments and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended. Any alterations and further modifications in the described embodiments, and any further applications of the principles of the invention as described herein are contemplated as would normally occur to one skilled in the art to which the invention relates.
The present invention provides a novel manner of sealing adjacent components of an electrochemical device to prevent the leakage of gases between the components. In accordance with one aspect of the invention, a multi-layer seal is positioned at the junction between two adjacent components of an electrochemical device and a compressive force is applied to the components and the seal to achieve sealing. Referring to the embodiment set forth in
It is readily understood that in electrochemical devices, it is often necessary to maintain discrete electrical circuits, of which certain components of the electrochemical device often are an integral part. As such, it is often important to use a non-conducting or insulating seal between the components to prevent electrical shorting within the device. In certain embodiments of the invention, gasket body 110, 210 comprises a non-conducting material. In other embodiments, at least one of interlayers 120, 130, 220, 230 comprises a non-conducting material. In yet other embodiments, gasket body 110, 210 and interlayers 120, 130, 220, 230 are formed of non-conducting materials.
In one embodiment, the gasket body comprises mica. The term “mica” encompasses a group of complex aluminosilicate minerals having a layer structure with varying chemical compositions and physical properties. More particularly, mica is a complex hydrous silicate of aluminum, containing potassium, magnesium, iron, sodium, fluorine and/or lithium, and also traces of several other elements. It is stable and completely inert to the action of water, acids (except hydro-fluoric and concentrated sulfuric) alkalies, convention solvents, oils and is virtually unaffected by atmospheric action. Stoichiometrically, common micas can be described as follows:
AB2-3(Al, Si)Si3O10(F, OH)2
where A=K, Ca, Na, or Ba and sometimes other elements, and where B=Al, Li, Fe, or Mg. Although there are a wide variety of micas, the following six forms make up most of the common types: Biotite (K2(Mg, Fe)2(OH)2(AlSi3)10)), Fuchsite (iron-rich Biotite), Lepidolite (LiKAl2(OH, F)2(Si2O5)2), Muscovite (KAl2(OH)2(AlSi3O10)), Phlogopite (KMg3Al(OH)Si4O10)) and Zinnwaldite (similar to Lepidolite, but iron-rich). Mica can be obtained commercially in either a paper form or in a single crystal form, each form of which is encompassed by various embodiments of the invention. Mica in paper form is typically composed of mica flakes and a binder, such as, for example, an organic binder such as a silicone binder or an epoxy, and can be formed in various thicknesses, often from about 50 microns up to a few millimeters. Mica in single crystal form is obtained by direct cleavage from natural mica deposits, and typically is not mixed with polymers or binders.
Micas are cleavable in the direction of the basal plane, which permits them to split easily into optically flat films, sometimes as thin as one micron in thickness. When split into thin films, they remain tough and elastic even at high temperature. Many forms of mica are transparent, colorless in thin sheets, resilient and generally incompressible. With respect to electrical properties, mica has the unique combination of great dielectric strength, uniform dielectric constant and capacitance stability, low power loss (high Q factor), high electric resistivity and low temperature coefficient and capacitance. It is noted for its resistance to arc and corona discharge with no permanent injury and has little or no effect when exposed to electronic radiation dosages up to 1018 ivt. With respect to thermal properties, mica is fire proof, infusible, incombustible, and non-flammable and can resist temperatures in excess of 600° C., and significantly higher, depending upon the type of mica. It has low heat conductivity, excellent thermal stability, and may be exposed to high temperatures without noticeable effect. Mica is also relatively soft and can be hand cut, machined or die-punched. It is flexible, elastic and tough, having high tensile strength, and can withstand great mechanical pressure perpendicular to plane but the lamination has cleavage and can be easily split into very thin leaves.
In one embodiment of the present invention, Muscovite is selected for use as the gasket body. In another embodiment, the gasket body comprises Muscovite in single crystal form. In yet another embodiment, the gasket body comprises Muscovite in paper form. In still another embodiment, Phlogopite is selected for use as the gasket body. In another embodiment, the gasket body comprises Phlogopite in single crystal form. In yet another embodiment, the gasket body comprises Phlogopite in paper form. In another embodiment, the gasket body comprises a mica selected from the group consisting of Biotite, Fuchsite, Lepidolite, Muscovite, Phlogopite and Zinnwaldite. In another embodiment, the gasket body comprises synthetic mica, a variety of forms of which are available commercially. It is also contemplated that other materials can be selected for use in accordance with the invention as the gasket body as would occur to a person of ordinary skill in the art. It is well within the purview of a person of ordinary skill in the art to select a mica or other material for use in forming the gasket body, depending upon the type of electrochemical device being constructed, and the operations conditions of the device. In one embodiment of the invention, the gasket body has a thickness of from about 25 microns to about 2 millimeters.
As described above, the multi-layer seal also includes a compliant interlayer on each opposing surface of the gasket body. As used herein, the term “compliant” is intended to refer to a property of the material whereby, under operating conditions of the electrochemical device, the material has a degree of plastic deformation under a given compressive force to block gas leakage pathways through the junction. Such gas leakage pathways can result, for example, from defects in the adjacent surfaces of the components, or other irregularities in the surfaces, including grooves on a metal component or grooves or voids on a ceramic component. Materials that can be used to form the compliant interlayers in various embodiments include, for example and without limitation, a glass, a glass-ceramic, a mica glass-ceramic, a phase-separated glass, a glass composite, a cermet, a metal, a metal alloy and a metal composite. To make a multi-layer seal in accordance with the invention, compliant interlayers can be applied to the gasket body in a variety of manners, including, for example and without limitation, dip-coating, painting, screen printing, deposition, spattering, tape casting and sedimentation. In addition, the compliant interlayer material can be provided in a variety of forms, including, for example, as fibers, granules, powders, slurries, liquid suspensions, pastes, ceramic tapes, metallic foils and others.
As stated above, compliant interlayers deform under a compressive force and under operating conditions of an electrochemical device to conform to the surfaces, including surface irregularities, of adjacent components, and to thereby provide a barrier to leakage of gases under operating temperatures and conditions of the electrochemical device. An important feature of the invention is the ability of at least one of the material interfaces at the junction, such as, for example, a component/interlayer interface or an interlayer/gasket body interface, to remain unbonded during operation of the electrochemical device, including heating and/or cooling cycles. As used herein, the term “unbonded” with respect to such materials at an interface is intended to mean that the components in contact at the interface are free to move (i.e., expand, contract or slide) independently of one another. Thus, during heating and/or cooling of the electrochemical device, the first component, first interlayer, gasket body, second interlayer and second component do not form a rigid mass, as occurs, for example, in devices having glass seals, which melt under operating temperatures and then rigidly bond adjacent parts to one another upon cooling.
In one embodiment of the invention, an interlayer of the multi-layer seal comprises a compliant material, such as, for example, a metallic material, that has a melting temperature greater than the operating temperature of an electrochemical device in which the multi-layer seal is to be used. In this embodiment, the interlayer does not melt, and does not become bonded to a component or the gasket body under operating conditions. In another embodiment, the gasket body comprises mica, which has been found by the present inventors to be satisfactorily resistant to bonding with materials it contacts during operation at high temperatures whether or not the interlayer comprises a materiel that melts under the operating temperatures. In another embodiment, the mica is a single crystal mica. While it is not intended that the present invention be limited by any theory whereby it achieves its advantageous result, it is believed that an interlayer that melts under operating temperatures may bond to the surface of a single crystal mica upon cooling, but that the physical properties of the mica allows a few sublayers of the mica crystal to cleave from the gasket body, thus maintaining a non-bonded interface.
In one embodiment, the compliant interlayer comprises glass. Although a wide variety of glass compositions can be used, as would occur to a person of ordinary skill in the art, it is important that the glass composition selected for use have a softening point lower than or equal to the operating temperature of the device in which the seal is to be used. Softening point, or softening temperature, of glass is defined under ASTM C338 as the temperature at which a uniform fiber of glass (0.55-0.75 mm diameter and 23.5 cm length) elongates under its own weight at 1 mm/min when the upper 10 cm is heated at 5° C./min. For glass having a density of 2.50 g/cc, this corresponds to a viscosity of about 106.6 Pa.s. It is also desirable when selecting a glass composition for the interlayer to select a glass composition that is not corrosive to surfaces of the components that come into contact with the interlayer under operating conditions, such as, for example, metallic components, ceramic components, and the gasket body. In one embodiment, the glass composition selected for use is an aluminosilicate glass. In another embodiment, the glass composition selected for use is a borosilicate glass. In another embodiment, the glass selected for use includes an alkaline earth element, such as, for example, strontium, magnesium and/or calcium, or an alkali additive, such as, for example, sodium, potassium and/or lithium. In other embodiments the interlayer comprises a glass-ceramic material (i.e., a glass-ceramic material as described in Lahl et al., “Aluminosilicate glass ceramics as sealant in SOFC stacks,” in Solid Oxide Fuel Cells (SOFC VI) Proceedings of the Sixth International Symposium., edited by S. C. Singhal and M. Dokiya, The Electrochemical Society, Proceedings Volume 99-19, 1057-1065 (1999)) or a mica glass-ceramic material (i.e., a mica glass-ceramic material as describe in Yamamoto et al, “Compatibility of mica glass-ceramics as gas-sealing materials for SOFC,” Denki Kagaku 64 [6] 575-581 (1996)).
In another embodiment of the invention, the multi-layer seal comprises at least one metallic interlayer. In one embodiment, the metallic interlayer comprises a noble metal, such as, for example, gold, silver, palladium, or platinum. In another embodiment, the metallic interlayer comprises a high-temperature alloy. It is also contemplated that other metals can be used that are resistant to oxidation under operating conditions of the electrochemical device. Metallic interlayers can be conveniently provided in the form of a metallic foil, such as a foil having a thickness of from about 0.005 mm to about 1 mm. In another embodiment, the metallic foil has a thickness of from about 0.01 mm to about 0.5 mm. In one embodiment of the invention, the interlayer comprises silver. In another embodiment, the interlayer comprises a silver foil having a thickness of from about 1 mil (25 microns) to about 10 mil (250 microns). In still another embodiment, the interlayer comprises a silver foil having a thickness of about 5 mils. Metallic layers comprising other metals in various embodiments can also be provided in the form of foils, including foils having thicknesses as set for above.
To seal a junction between adjacent components of an electrochemical device, a multi-layer seal as provided herein is positioned between the adjacent components such that each compliant interlayer is positioned between the gasket body and one of the components. Sealing is then accomplished by applying a compressive force to the components and the seal to maintain the seal in position and to cause the compliant interlayers to mold to surface defects in the surfaces of the components and the gasket body under operating conditions of the device. In one embodiment of the invention, the compressive force is a force of from about 5 to about 500 pounds per square inch (psi). In another embodiment, the compressive force is a force of from about 10 to about 400 psi. In another embodiment, the compressive force is a force of from about 15 to about 300 psi.
In operation of an electrochemical device including an inventive seal, the temperature of the seal increases as the temperature of the electrochemical device increases toward its normal operating temperature. In an embodiment comprising a glass interlayer, as the temperature increases beyond the softening temperature of the glass, the glass, under the compressive force, deforms to mold to surface irregularities. When a metallic interlayer is used, the same phenomenon occurs if the operating temperature of the electrochemical device exceeds the melting point of the metallic material selected for use. Even if the operating temperature does not exceed the melting point of the metallic material, the metallic interlayer selected for use in accordance with the invention deforms under the compressive force to effectively form a barrier to leakage of gases through the junction during operation of the device.
It is readily understood that a variety of electrochemical devices, such as, for example and without limitation, solid oxide fuel cells, syngas membrane reactors, and oxygen generators, have a plurality of adjacent functional units to increase the efficiency of the device and to increase output of the device to a more useful level, whether the output of the device is electricity, synthetic gas, oxygen or other. Arrangement of a plurality of units is often accomplished by providing stacked planar units. It is readily understood that such planar units act as boundaries between diverse gaseous streams, and, when in a stacked arrangement, form a plurality of junctions therebetween.
In one aspect of the invention, therefore, an electrochemical device having a plurality of adjacent components is provided that includes an inventive multi-layer seal positioned at one or more junction, preferably at multiple junctions. In a preferred embodiment, the device includes an inventive multi-layer seal at each such junction. Referring now to
In one embodiment of the invention, the electrochemical device is a solid oxide fuel cell (“SOFC”) assembly for electrochemically reacting a fuel gas with a flowing oxidant gas at an elevated temperature to produce a DC output voltage. The SOFC includes a plurality of generally planar integral fuel cell units. Referring, for example to
As will be appreciated by a person of ordinary skill in the art in view of the present description, in one form of the present invention, a multi-layer seal for sealing a junction between adjacent components of an electrochemical device is provided. The multi-layer seal includes a gasket body defining first and second opposing surfaces; a first compliant interlayer positioned adjacent the first surface; and a second compliant interlayer positioned adjacent the second surface. In one embodiment, the opposing surfaces of said gasket body are configured to correspond to junction surfaces of the adjacent components of the electrochemical device. In another embodiment, each of said first and second compliant interlayers is positioned to be disposed between the gasket body and the junction surface of one of the adjacent components. In yet another embodiment, the gasket body comprises a single crystal mica or a mica paper. The mica can be, for example, Muscovite, Phlogopite, Biotite, Fuchsite, Lepidolite or Zinnwaldite. In still another embodiment, the at least one of the compliant interlayers comprises a member selected from the group consisting of a glass, a glass-ceramic, a mica glass-ceramic, a phase-separated glass, a glass composite, a cermet, a metal, a metal alloy and a metal composite.
In one preferred embodiment, at least one of the compliant interlayers comprises glass. In another embodiment, the glass has a softening point lower than or equal to the operating temperature of the electrochemical device. In another preferred embodiment, at least one of the compliant interlayers comprises a metal. In another embodiment, the metal is selected from the group consisting of gold, silver, palladium and platinum. In still another embodiment, at least one of the compliant interlayers is a metallic foil having a thickness of from about 0.005 millimeters to about 1 millimeter. In yet another embodiment, at least one of the compliant interlayers is a metallic foil having a thickness of from about 0.01 millimeters to about 0.5 millimeters.
In another form of the invention, an electrochemical device is provided that includes a plurality of components, the components forming at least one boundary between diverse gaseous streams and defining at least one junction between the components. A multi-layer seal is positioned at the junction, the seal composed of a gasket body disposed between two compliant interlayers. With the seal thus positioned, each compliant interlayer is positioned between the gasket body and one of said components. The electrochemical device also includes a compression member for exerting a compressive force to the components and the seal.
In certain embodiments, the seal is a non-conducting seal. In one embodiment, the gasket body comprises mica. In another embodiment, the gasket body of the multi-layer seal has a thickness of from about 25 microns to about 2 millimeters. In yet another embodiment, at least one of the compliant interlayers comprises glass. In certain embodiments, the glass has a softening point lower than or equal to the operating temperatures of the device. The glass is preferably a glass that is not corrosive to surfaces of the components in contact with the glass under operating conditions. In one embodiment, the glass composition selected for use is an aluminosilicate glass. In another embodiment, the glass composition selected for use is a borosilicate glass. In another embodiment, the glass selected for use includes an alkaline earth element, such as, for example, strontium, magnesium and/or calcium, or an alkali additive, such as, for example, sodium, potassium and/or lithium. In yet another embodiment, each of the glass interlayers has a thickness of from about 0.005 millimeters to about 5 millimeters prior to heating. In still another embodiment, the glass interlayer has a thickness of from about 0.05 millimeters to about 0.5 millimeters prior to heating.
In another embodiment of the electrochemical device, at least one of the compliant layers comprises a metal. The metal selected for use is preferably resistant to oxidation under operating conditions of the device. In one embodiment, the metal is selected from the group consisting of gold, silver, palladium and platinum. In another embodiment, the compliant interlayer is a metallic foil having a thickness of from about 0.005 millimeters to about 1 millimeter prior to heating.
Another form of the invention is a method for making a multi-layer seal, comprising (1) providing a gasket body defining first and second generally flat opposing surfaces; and (2) applying a compliant material to said first and second surfaces to form first and second compliant interlayers. In certain embodiments, the gasket body comprises mica and/or at least one of the compliant interlayers comprises a member selected from the group consisting of a glass, a glass-ceramic, a mica glass ceramic, a phase-separated glass, a glass composite, a cermet, a metal, a metal alloy and a metal composite. The compliant material can be applied to the first and second surfaces of the gasket body, for example, by dip-coating, painting, screen printing, deposition, spattering, tape casting or sedimentation.
In another form of the invention, there is provided a method for sealing a junction between adjacent ceramic or metallic components of an electrochemical device, comprising (1) positioning between the adjacent components a multi-layer seal composed of a gasket body disposed between a first compliant interlayer and a second compliant interlayer, wherein each of the first and second compliant interlayers is positioned between the gasket body and one of the components; and (2) applying a compressive force to the components and the seal. In one embodiment, the compressive force is a force of from about 5 to about 500 psi.
In another form of the invention, there is provided a solid oxide fuel cell assembly for electrochemically reacting a fuel gas with a flowing oxidant gas at an elevated temperature to produce a DC output voltage, said solid oxide fuel cell. The SOFC assembly includes a plurality of generally planar integral fuel cell units, each unit comprising a layer of ceramic ion conducting electrolyte disposed between a conductive anode layer and a conductive cathode layer, and the units are arranged one on another along a longitudinal axis perpendicular to the planar units to form a fuel cell stack. The assembly also includes a multi-layer non-conducting seal disposed between the anode layer and the cathode layer of adjacent fuel cell units. The seal is composed of a gasket body disposed between two compliant interlayers. The assembly also includes a compression member for exerting a compressive force along the longitudinal axis. In one embodiment, the compressive force is a force of from about 5 to about 500 psi.
Reference will now be made to specific examples illustrating various preferred embodiments of the invention as described above. It is to be understood that the examples are provided to illustrate preferred embodiments and that no limitation to the scope of the invention is intended thereby.
1. Plain Mica Seal (Compressive Mica Seals)
Three micas were used in this study: Muscovite (KAl2(AlSi3O10)(F,OH)2) paper, cleaved Muscovite single crystal sheet, and Phlogopite (KMg3(AlSi3O10)(OH)2) paper. All three micas are about 0.1 mm thick. The Muscovite mica loses about 4% chemical water at about 600° C. Phlogopite mica is more stable in high temperatures, losing its chemical water at about 950° C. The paper-type micas are composed of discrete large mica flakes bonded with organic binders, and pressed into thin sheets.
Mica samples 410 were cut into 1½ inch squares with a ½ inch diameter central hole. The mica squares 410 were then pressed between an Inconel tube 420 (outer diameter=1.3 inch and inner diameter=1.0 inch) and a dense alumina substrate 430. Samples were heated in a clamshell furnace 440 at a heating rate about 2° C./min to 800° C. The load was applied using a universal mechanical tester 450 with a constant load control (Model 5581, Instron, Canton, Mass.). The experimental setup is shown schematically as in
L=Δn/Δt=(nf−ni)/(tf−ti)=(pf−pi)V/RT(tf−ti)
where n is the moles of the gas, T is the temperature, V is the reservoir volume, R is the gas constant, t is the time, and p is the pressure. Subscripts f and i represent the final and the initial conditions. The calculated leak rate (L, in standard cubic centimeters per minute at STP, sccm) was further normalized with respect to the outer leak length (10.5 cm) of the Inconel tube and to a pressure gradient of 2 psi by the equation:
Thus, the unit for leak rate is standard cubic centimeters per minute per centimeter (“sccm/cm”) and STP and with a pressure gradient of 2 psi.
Before each run, the leak rate of the background (or the system without test samples) was also measured and subtracted from the actual test runs. To ensure a constant temperature, all leak tests were conducted about ½ hour after reaching the desired temperatures (800° C.).
Data collected for the plain mica seal comparative test runs is set forth in Table I below.
2. Rigid Glass Seal
For comparison, a test of a glass-only seal was also conducted using the same setup as described above and using a single layer of glass without the mica sheet. It is worthy of note that, irrespective of the form of the glass prior to the test, the glass softened at the temperatures used in the test, and then resolidified as the apparatus cooled after testing to form a rigid glass seal. For a rigid glass seal, it was found that the leak rate was about 5×10−5 sccm/cm at 800° C. at a pressure gradient of 2 psi, using the current test setup. Ideally, the leak rate should be zero for a hermetic seal if the glass wets the surfaces in contact. In reality, the actual low leak rates were limited by the system's background since there were valves and tube connectors in the setup.
3. Discussion of Comparative Data
As for the compressive mica seals, Simner et al. reported a leak rate of 0.65 sccm/cm at the same conditions and a compressive stress of 100 psi using the Muscovite single crystal sheet (about 0.1 mm thick). (S. P. Simner and J. W. Stevenson, “Compressive mica seals for SOFC applications,” J. Power Sources, 102 [1-2] 310-316 (2001)). It is appropriate to ask why the apparently flexible thin mica sheet allowed a leak rate about 104 times higher than that of a glass seal (the as-received Muscovite single crystal sheet, though relatively stiff in its as-received form, becomes flexible (and fragile) when heated to 800° C.). Looking at a compressed mica between the Inconel tube and the alumina substrate, one can imagine there are two possible paths for leaks. One is from the interface between the metal tube (or the ceramic substrate) and the mica. The other one is through the mica itself, since it cleaves into many sub-layers after losing its chemically bonded water at elevated temperatures (Simner et al.). Looking at the surfaces of the contact materials (dense alumina as the support substrate and the Inconel tube as the top pressing ram,
The same protocol was used as in Example 1, but the mica seals were replaced with multi-layer seals, in which glass interlayers 412, 414 were placed between the Inconel tube 420/mica 416 and mica 416/alumina 430 interfaces as shown in
It is seen that the best results were obtained using Muscovite single crystal mica. The normalized leak rate for this seal at 800° C. was only 1.55×10−4 sccm/cm at a stress of 100 psi and a pressure gradient of 2 psi, which is a leak rate about 4300 times lower than the leak rate of a simple mica seal at this temperature. Seals based on the other commercial micas (Muscovite and Phlogopite mica papers), also exhibited superior leak rates (about 0.011 sccm) compared to simple mica seals without the compliant glass interlayer (about 6 to about 9 sccm/cm).
The multi-layer seals with glass interlayers are shown to exhibit excellent sealing function for electrochemical devices, considering the low leak rates reported above. For a 60-cell (14 cm×14 cm active area per cell) stack, producing 0.5 W/cm2 or 5.9 kW total gross power on steam reformed methane (steam to carbon mole ratio of 3.0), at 65% fuel utilization, 20% oxygen utilization, the total reformate gas flow rate entering the anode is estimated to be 1.36×105 sccm (STP). Assuming that the leak rate (per cm of seal length) measured in this study applied to full size stacks, the total leak rate for a 60-cell stack at 800° C. would be only 0.0019% of the total fuel rate for the multi-layer seal including a Muscovite single crystal mica gasket body and glass interlayers under a stress of 25 psi and a 2 psi pressure gradient (a leak length of 124 cm was assumed for each layer).
The microstructure of the mica was examined before and after the 800° C. leak tests using scanning electron microscopy to assess whether the use of a low melting glass as the seal interlayer could damage the materials with which it is in contact (e.g., metal, ceramic, and the mica itself), especially under the compressive stresses. Though long-term stability tests are underway, preliminary results showed no substantial corrosion or melting of the materials in contact. The corrosion at the glass metal/interface was limited to a depth of a few microns. This may result from the fact that the majority of the glass was squeezed out from between the components at elevated temperatures under the compressive stresses. If only a thin glass interlayer is left behind, only limited corrosion or melting would be likely to occur. As for the mica itself, degradation might be expected due to interaction between the mica (an aluminosilicate) and the borosilicate glass, but no significant degradation was observed. The mica remained intact except for a few surface sub-layers which bonded to the metal tube and the ceramic substrate when the test specimens were disassembled after testing.
The 800° C. leak rates for the three micas, with and without glass interlayers and at various compressive stesses are summarized in Table III below.
The results are also plotted as a function of the compressive stresses for Muscovite single crystal mica sheet (
It is also interesting to note that the effect of increasing the applied compressive stress was much weaker for the multi-layer seals than for the plain mica seals. This is especially clear for the paper-type micas. For example, the leak rate reduced about 81% (from 8.85 sccm/cm to 1.68 sccm/cm) for Phlogopite mica paper when the compressive stress increased 400% from 100 psi to 500 psi. For the multi-layer form, the leak rate only reduced about 10% (from 0.0108 sccm/cm to 0.0098 sccm/cm) for a 300% increase in the stress from 100 psi to 400 psi. Similar results were also evident for the Muscovite mica paper. No substantial difference was observed between the Phlogopite mica paper and the Muscovite mica paper, though the former is more stable at higher temperatures than the latter. These results are consistent with previously reported data. Simner et al. reported a similar reduction for a thicker Phlogopite paper (0.5 mm) while using high purity helium at a 2 psi positive pressure gradient; in that study the leak rate dropped about 85% from 6.26 sccrncm to 0.97 sccm/cm when the applied stress increased from 100 psi to 500 psi. (Simner et al.).
In the case of the Muscovite single crystal mica, there was a strong dependence on the applied compressive stress for both the multi-layer seals and the plain mica seals. However, the stress range for the multi-layer seal with single crystal mica was only from 25 psi to 100 psi (at higher stresses the leak rates were close to the system's background, so tests were not conducted). It is expected that the multi-layer seal with single crystal mica would also show less dependence on stress at higher compressive loads since the sub-layers (after the loss of chemical water at elevated temperatures
Overall, it is clear that the Muscovite single crystal micas offer superior performance to the mica papers in multi-layer seals; for example, the leak rate for a Muscovite multi-layer seal was only 3.59×10−4 sccm/cm at a low compressive stress of 25 psi. Based upon microstructural examination of these materials, this is likely due to the fact that the paper type micas are composed of discrete mica flakes/platelets, so that the leak paths are 3-dimensional, whereas the single crystal micas tend to have only 2-dimensional leak paths (through the cleavage planes). Though the single crystal mica sheets did form some defects after the loss of chemical water at elevated temperatures, these defects (micro-cracks) were minute in size compared to the connected voids which were prevalent in the mica papers.
The protocol set forth in Example Two was repeated using a multi-layer seal composed of a mica gasket body and two compliant metallic interlayers. The metallic material used as the compliant layers in these tests was silver in the form of a thin foil.
The results of testing of multi-layer seals having metallic interlayers are set forth in Table IV below, which also includes data for the plain compressive mica seals and multi-layer seals with glass interlayers, as set forth in Table III.
It is seen that the leak rates are also greatly reduced for the multi-layer seals with metallic interlayers as compared to plain compressive mica seals. It is also seen that the best results were again obtained using Muscovite single crystal mica. The normalized leak rate for the multi-layer seal with 5 mil silver interlayers at 800° C. was only 8.9×10−4 sccm/cm at a stress of 100 psi and a pressure gradient of 2 psi, which is a leak rate about 740 times lower than the leak rate of a simple mica seal at this temperature. Seals based on the other commercial micas (Muscovite and Phlogopite mica papers), also exhibited superior leak rates (about 9.5×10−2 sccm/cm) compared to simple mica seals without the compliant metallic interlayer (about 6 to about 9 sccm/cm).
The multi-layer seals with metallic interlayers are also shown to exhibit excellent sealing function for electrochemical devices, considering the low leak rates reported above. For a 60-cell (14 cm×14 cm active area per cell) stack, producing 0.5 W/cm2 or 5.9 kW total gross power on steam reformed methane (steam to carbon mole ratio of 3.0), at 65% fuel utilization, 20% oxygen utilization, the total reformate gas flow rate entering the anode is estimated to be 1.36×105 sccm (STP). Assuming that the leak rate (per cm of seal length) measured in this study applied to full size stacks, the total leak rate for a 60-cell stack at 800° C. would be only 0.026% of the total fuel rate for the multi-layer seal including a Muscovite single crystal mica gasket body and metallic interlayers under a stress of 25 psi and a 2 psi pressure gradient (a leak length of 124 cm was assumed for each layer).
Leak rates were also determined for the three micas at various compressive pressures, and the results are summarized in Table IV above. Table IV includes data of the multi-layer seals (with glass interlayers and metallic interlayers) and the plain compressive mica seals. The results are also plotted as a function of the compressive stresses for Muscovite single crystal mica sheet (
The effect of increasing the applied compressive stress was also much weaker for the multi-layer seals with metallic interlayers than for the plain mica seals. This is especially clear for the paper-type micas. For example, the leak rate reduced about 81% (from 8.85 sccm/cm to 1.68 sccm/cm) for Phlogopite mica paper when the compressive stress increased 400% from 100 psi to 500 psi (Table 1). For the multi-layer form, the leak rate only reduced about 62% (from 9.8×10−2 sccm/cm to 3.7×10−2 sccm/cm) for the same increase in the stress. Similar results were also evident for the Muscovite mica paper. No substantial difference was observed between the Phlogopite mica paper and the Muscovite mica paper, though the former is more stable at higher temperatures than the latter. These results are also consistent with previously reported data.
The thickness variation along the pressed ring (1.3 inch outside diameter, and 1.0 inch inner diameter) sections was measured with a digital micrometer along the 12 hour positions. Alumina substrate was found to be more uniform in the thickness (with a maximum thickness of 514 microns and a minimum thickness of 507 microns), whereas the as-received Muscovite single crystal mica varies more in the thickness (with a maximum thickness of 122 microns and a minimum thickness of 107 microns). In view of the 7 micron fluctuation on the Alumina substrate surface and the 15 micron fluctuation in the mica surface, the worst-case gap between the surfaces would be 7+15=22 microns. A determination of surface variation was not made for the Inconel tube surface.
The difference in
A simulated multiple component assembly was also tested. In this test, six multi-layer seals having gasket bodies of Muscovite single crystal mica and borosilicate glass interlayers were used. Five layers of metal sheet (SS 430 with a nominal sheet thickness of 0.010 inches) were placed between the multi-layer seals, as depicted in
It is evident that the multi-layer seal showed very good stability under thermal cycling. Optical microscopy also confirmed that no melting of mica was observed and the individual layers (SS430 and mica layers) were easily separated after the test.
While the invention has been illustrated and described in detail in the drawings and foregoing description, the same is to be considered as illustrative and not restrictive in character, it being understood that only selected embodiments have been shown and described and that all changes, equivalents, and modifications that come within the spirit of the invention described herein or defined by the following claims are desired to be protected. Any experiments, experimental examples, or experimental results provided herein are intended to be illustrative of the present invention and should not be considered limiting or restrictive with regard to the invention scope. Further, any theory, mechanism of operation, or finding stated herein is meant to further enhance understanding of the present invention and is not intended to limit the present invention in any way to such theory, mechanism or finding. All publications, patents, and patent applications cited in this specification are herein incorporated by reference as if each individual publication, patent, or patent application were specifically and individually indicated to be incorporated by reference and set forth in its entirety herein.
This application is a divisional of U.S. application Ser. No. 10/134,072, filed Apr. 26, 2002 now U.S. Pat. No. 7,222,406, which is incorporated herein by reference.
This invention was made with Government support under Contract Number DE-AC0676RLO1830 awarded by the U.S. Department of Energy. The Government has certain rights in the invention.
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Number | Date | Country | |
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Parent | 10134072 | Apr 2002 | US |
Child | 11224881 | US |