Patent Application
20090220813
The present invention relates to alloys for joining metal materials by brazing; more particularly, to silver-containing braze alloys for joining ceramics to metals; and most particularly, to silver braze alloys containing non-fusible particles to control joint thickness during fusing of the alloy.
Fuel cells which generate electric current by controllably combining elemental hydrogen and oxygen are well known. In one form of such a fuel cell, an anodic layer and a cathodic layer are separated by a permeable electrolyte formed of a ceramic solid oxide, such as yttrium-stabilized zirconium (YSZ). Such a fuel cell is known in the art as a “solid oxide fuel cell” (SOFC). A single cell is capable of generating a relatively small voltage and wattage, typically between about 0.5 volt and about 1.0 volt, depending upon load, and less than about 2 watts per cm2 of cell surface. Therefore, in practice it is known to stack together, in electrical series, a plurality of cells.
In a currently-preferred arrangement, each ceramic-based fuel cell is bonded to a surrounding metal “cassette” frame to form a fuel cell sub-assembly, using a silver/copper-based braze. As the solid braze alloy is liquefied, the copper is rapidly oxidized to form copper oxide which separates from the alloy, leaving essentially pure silver as the brazing material. The copper oxide migrates to the boundaries of the liquid and adheres to the ceramic and the metal, providing an attachment layer for the silver. Exemplary silver/copper and silver/vanadium braze alloys are disclosed in International Publication No. WO 03/059843, published 24 Jul. 2003, which is incorporated herein by reference.
A problem in the use of such alloys is that the liquidus range of the alloy is very small, such that the alloy tends immediately to become very runny upon melting and is easily squeezed out of a mechanical joint, leaving a weak bond which is easily fractured. This is known in the art of bonding as a “dry joint.” Further, the alloy displaced from the joint can flow onto adjacent areas of the apparatus being brazed, such as a fuel cell assembly, which can lead to electrical shorts during later attempted use of the apparatus. In addition, if the joint gap is too large due to insufficient loading or an out-of-flatness condition of the mating parts, the braze alloy will not fill the gap.
A known approach to the problem of retaining liquid braze in a joint is to provide one or both of the surfaces to be brazed with shallow dimples such that the local joint thickness at each dimple will be increased. This approach is less than satisfactory in some applications, in that the braze layer is thickened only in the regions of the dimples, rather than over the entire joint, and in that it may be undesirable or impossible to provide the required dimples on some surfaces to be brazed.
What is needed in the art is a means for maintaining a minimum joint thickness of a brazing alloy when brazing mating planar surfaces, and for reducing the tendency of the liquefied alloy to be squeezed from such a joint.
It is a principal object of the present invention to maintain a minimum joint thickness of a brazing alloy, to reduce the tendency of the liquefied alloy to flow from a joint, and to allow an additional load to be applied to the joint to maintain a minimum gap and/or to flatten the adjoining parts without causing a dry joint.
Briefly described, a minimum joint thickness can be assured, and liquid braze can be discouraged from running out of a joint, by incorporating into the braze material beads or particulates having a diameter corresponding to the minimum joint thickness desired and which are infusible at the brazing temperature. For example, in brazing SOFC fuel cell components, a desirable braze joint thickness is in the range of about 30 μm to about 50 μm. When infusible particles in that size range are incorporated into the braze alloy, the joint thickness is assured. Preferably such particles are formed of high-melting metals, metal oxides, ceramics, or cermets. Preferably, the particles are mixed into an alloy paste prior to fusing. In a preferred embodiment, the particle-containing paste is mixed with a non-flux carrier to facilitate application to the surfaces to be brazed. Exemplary application methods may include painting, rolling, screening, or extrusion dispensing. Brazing alloys in accordance with the invention are useful in bonding ceramics to ceramics, ceramics to metals, and metals to metals.
The present invention will now be described, by way of example, with reference to the accompanying drawings, in which:
Referring to
Braze alloy 22 includes a plurality of particles typified by particle 50, the particles being distributed throughout the alloy matrix 22′ and having a general diameter 52 equal to the desired thickness of the braze seal. Particles 50 thus act as shims or spacers to assure a desired seal thickness by limiting the degree to which molten braze may be extruded from the seal space. Of course, particle 50 may be irregular in shape, as shown, and may have a shorter diameter 54 which if oriented across the seal between elements 18 and 20 can result in a thinner seal; however, particles 50 preferably are selected such that, even if they are irregular and not preferentially orientable, the shortest diameter 54 will still provide a desired minimum thickness or seal. Of course, particles 50 may be provided as spherical beads (not shown), having a constant diameter equal to the desired seal thickness.
Particles or beads 50 may be formed in known fashion from metals, metal alloys, ceramics, and cermets, provided that the melting point of the material is sufficiently high that the particles are not fusible in the brazing range of temperatures. The melt temperature of the particles should be at least 50° C. higher than the brazing temperature range. For silver braze alloys, the melt temperature of the particles should preferable be above 1050° C. Such particulated alloys in accordance with the invention are especially useful in brazing metal and ceramic components of a solid-oxide fuel cell assembly.
For application to surfaces to be brazed, particulated alloys may be formed by mixing alloy powder or paste with an amount of the particulate material which has been previously comminuted and sorted to provide only particles in the desired size range or smaller. The particulate/alloy mixture may then be mixed with an evanescent non-flux carrier (not shown), for example, Ferro A149-19-15, available from Ferro Corp., Cleveland, Ohio, USA, to form a particulated slurry which is readily applied by known methods, for example, brushing, rolling, spraying, screening, or extrusion dispensing.
Preferably, a brazed joint is formed by:
a) applying a particulated slurry in accordance with the invention to one or both of the surfaces to be brazed;
b) engaging, under clamping pressure, the surfaces to be brazed; and
c) heating the clamped assembly above the braze alloy liquidus temperature to fuse the fusible metal, drive off the evanescent carrier, and collapse the joint until further collapse is prevented by the infusible particulates contained in the particulated braze alloy. The included particles can allow a higher clamping load to flatten adjoining parts to form a minimum gap providing an optimal joint thickness throughout the joint.
While the invention has been described by reference to various specific embodiments, it should be understood that numerous changes may be made within the spirit and scope of the inventive concepts described. Accordingly, it is intended that the invention not be limited to the described embodiments, but will have full scope defined by the language of the following claims.
This is a continuation application of U.S. patent application Ser. No. 11/638,192, filed Dec. 13, 2006, which is a divisional of U.S. patent application Ser. No. 10/892,591, filed Jul. 15, 2004, that issued as U.S. Pat. No. 7,179,558.
The present invention was supported in part by a U.S. Government Contract, Number DE-FC26-02NG41246. The United States Government may have rights in the present invention.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10892591 | Jul 2004 | US |
| Child | 11638192 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11638192 | Dec 2006 | US |
| Child | 12386120 | US |
