The invention relates to a microheat exchanger and a method of fabrication of the same. More particularly, this invention relates to a microheat exchanger and a method of fabrication, where the microheat exchanger is used for laser diode cooling.
Microheat exchangers are made of thermally conductive material and are used to transfer heat from a heat generating device, such as an integrated circuit or a laser diode, to a fluid flowing through fluid pathways within the microheat exchanger. Microheat exchangers are commonly made of metal, such as copper, and electrical isolation is often required between the heat generating device and the microheat exchanger. Some ceramic materials are thermally conductive yet electrically resistant. For this reason, such ceramic materials are often used as an intermediate material between a heat generating device and a microheat exchanger to provide electrical isolation while still maintaining thermal conductivity. However, it is not practical to connect a heat generating device directly to ceramic. Instead, the heat generating device is coupled to a conductive pad, typically made of a conductive metal such as copper. In such a configuration, the ceramic is middle layer between the conductive copper pad coupled to the heat generating device and the microheat exchanger.
In order to provide efficient heat transfer from the heat generating device to the microheat exchanger, a good thermal interface between ceramic and copper is necessary. A direct bonded copper (DBC) method uses a high temperature joining process to bond a copper sheet to a ceramic plate in the presence of a protective gas atmosphere having small amounts of oxygen (50-200 ppm). Exemplary DBC methods are described in U.S. Pat. No. 6,297,469 and U.S. Pat. No. 7,036,711, which are hereby incorporated in their entirety by reference. Three commonly used ceramic materials are beryllium oxide (BeO), aluminum oxide (Al2O3), and aluminum nitride (AlN). Oxygen and copper bond together under high temperature. The copper and ceramic are heated to a carefully controlled temperature, in an atmosphere of nitrogen and a small percentage of oxygen. The temperature used is in the range between 1950 and 1981 degrees Fahrenheit, which is close to the melting temperature of copper. Under these conditions, a copper-oxygen eutectic forms which bonds successfully both to copper and the ceramic, thereby bonding a copper layer to a ceramic layer. The copper layer is used as a conductive pad to be coupled to a heat generating device. The ceramic layer is typically soldered to the top of the microheat exchanger.
Many problems exist with bonding in general and the DBC technique in particular. First, application of high temperature to rigid ceramic plates often results in cracking of the ceramic. Second, microvoids are formed at the interface of the bonded copper and ceramic layers. The microvoids are due to the imperfections and irregularities in the contact surfaces of the copper and ceramic layers. For applications where a large heat generating device, or multiple heat generating devices are coupled to a single ceramic plate, the size of the ceramic plate is larger. However, the larger the ceramic plate, the greater the impact of the microvoids. Presence of microvoids reduces thermal efficiency. Further, presence of microvoids increases the chances that the copper layer and the ceramic layer will delaminate because there is not a perfect bond across the entire interface surface.
Third, the thermal coefficient of expansion for copper is much greater than that for ceramic. During the high temperature DBC process, the copper layer expands more so than the ceramic, at which point the ceramic layer and the copper layer are bonded. However, upon cooling the copper layer contracts more so than the ceramic, due to the differing thermal coefficients of expansion, which leads to warping and possible cracking of the bonded copper-ceramic assembly.
A microheat exchanging assembly is configured to cool one or more heat generating devices, such as integrated circuits or laser diodes. In some embodiments, the microheat exchanging assembly includes a first ceramic assembly thermally coupled to a first surface, and in some embodiments, a second ceramic assembly thermally coupled to a second surface. Each ceramic assembly includes one or more electrically and thermally conductive pads, each conductive pad is electrically isolated from each other. Each ceramic assembly includes a ceramic layer to provide this electrical isolation. The ceramic layer has high thermal conductivity and high electrical resistivity. A top surface and a bottom surface of the ceramic layer are each bonded to a conductive layer, such as copper, using an intermediate joining material. A brazing process is performed to bond the ceramic layer to the conductive layer via a joining layer. The joining layer is a composite of the joining material, the ceramic layer, and the conductive layer. The top conductive layer and the joining layer are etched to form the electrically isolated conductive pads. The conductive layers are bonded to the ceramic layer using a bare ceramic approach or a metallized ceramic approach.
In one aspect, a device includes a heat exchanging device having a thermally conductive material, wherein the heat exchanging device is configured to transfer heat from the thermally conductive material to a fluid flowing therethrough; and a thermally conductive ceramic assembly thermally coupled to the heat exchanging device. The ceramic assembly includes a conductive layer; a ceramic layer; and an active brazing alloy bonded between the conductive layer and the ceramic layer to form a joining layer, wherein the conductive layer and the joining layer are configured to form one or more electrically isolated conductive pads. In some embodiments, the conductive layer and the joining layer are patterned to form a plurality of electrically isolated pads, further wherein each of the plurality of electrically isolated pads are electrically isolated from each other by the ceramic layer. In some embodiments, the ceramic assembly also includes a second conducive layer and a second active brazing alloy layer bonded between the second conductive layer and the ceramic layer to form a second joining layer. The device can also include a metal-to-metal joining layer bonded between the second conductive layer of the ceramic assembly and the heat exchanging device. In some embodiments, the conductive layer and the heat exchanging device are copper-based. In some embodiments, the ceramic layer includes beryllium oxide, aluminum oxide, or aluminum nitride. In some embodiments, the active brazing alloy is a copper-based active brazing alloy, a copper-silver-based active brazing alloy, or an indium-copper-silver-based active brazing alloy. In some embodiments, the active brazing alloy layer is an active joining material paste or an active joining material foil. The device can also include a second thermally conductive ceramic assembly thermally coupled to an opposite side of the heat exchanging device than the ceramic assembly.
In another aspect, a device includes a heat exchanging device comprising a thermally conductive material, wherein the heat exchanging device is configured to transfer heat from the thermally conductive material to a fluid flowing therethrough; and a thermally conductive ceramic assembly thermally coupled to the heat exchanging device. The ceramic assembly includes a conductive layer; a ceramic layer including a metallized first surface; and a joining material bonded between the conductive layer and the metallized first surface of the ceramic layer to form a joining layer, wherein the conductive layer, the joining layer, and the metallized first surface are configured to form one or more electrically isolated conductive pads. In some embodiments, the conductive layer and the joining layer are patterned to form a plurality of electrically isolated pads, further wherein each of the plurality of electrically isolated pads are electrically isolated from each other by the ceramic layer. The ceramic layer can also include a metallized second surface, and the ceramic assembly can also include a second conducive layer and a second joining material bonded between the second conductive layer and the metallized second surface of the ceramic layer to form a second joining layer. The device can also include a metal-to-metal joining layer bonded between the second conductive layer of the ceramic assembly and the heat exchanging device. In some embodiments, the conductive layer and the heat exchanging device are copper-based. In some embodiments, the ceramic layer is beryllium oxide, aluminum oxide, or aluminum nitride. In some embodiments, the metallized first surface includes molybdenum manganese and nickel. The device can also include a second thermally conductive ceramic assembly thermally coupled to an opposite side of the heat exchanging device than the ceramic assembly. In some embodiments, the joining material is a copper-silver paste, a copper-gold paste, a copper-silver foil, or a copper-gold foil. In other embodiments, the joining material and the conductive layer are a silver plated copper sheet.
In yet another aspect, a device includes a heat exchanging device comprising a thermally conductive material, wherein the heat exchanging device is configured to transfer heat from the thermally conductive material to a fluid flowing therethrough; and a thermally conductive ceramic assembly thermally coupled to the heat exchanging device. The ceramic assembly includes a ceramic layer including a metallized first surface; and a conductive layer plated to the metallized first surface, wherein the conductive layer and the metallized first surface are configured to form one or more electrically isolated conductive pads. In some embodiments, the conductive layer and the metallized first surface are patterned to form a plurality of electrically isolated pads, further wherein each of the plurality of electrically isolated pads are electrically isolated from each other by the ceramic layer. The ceramic layer can also include a metallized second surface, and the ceramic assembly can also include a second conductive layer plated to the metallized second surface. The device can also include a metal-to-metal joining layer bonded between the second conductive layer of the ceramic assembly and the heat exchanging device. In some embodiments, the conductive layer and the heat exchanging device are copper-based. In some embodiments, the ceramic layer is beryllium oxide, aluminum oxide, or aluminum nitride. In some embodiments, the metallized first surface includes molybdenum manganese and nickel. The device can also include a second thermally conductive ceramic assembly thermally coupled to an opposite side of the heat exchanging device than the ceramic assembly.
Other features and advantages of the microheat exchanging assembly will become apparent after reviewing the detailed description of the embodiments set forth below.
The microheat exchanging assembly is described relative to the several views of the drawings. Where appropriate and only where identical elements are disclosed and shown in more than one drawing, the same reference numeral will be used to represent such identical elements.
Reference will now be made in detail to the embodiments of the microheat exchanging assembly, examples of which are illustrated in the accompanying drawings. While the microheat exchanging assembly will be described in conjunction with the embodiments below, it will be understood that they are not intended to limit the microheat exchanging assembly to these embodiments and examples. On the contrary, the microheat exchanging assembly is intended to cover alternatives, modifications and equivalents, which may be included within the spirit and scope of the microheat exchanging assembly as defined by the appended claims. Furthermore, in the following detailed description of the microheat exchanging assembly, numerous specific details are set forth in order to more fully illustrate the microheat exchanging assembly. However, it will be apparent to one of ordinary skill in the prior art that the microheat exchanging assembly may be practiced without these specific details. In other instances, well-known methods and procedures, components and processes have not been described in detail so as not to unnecessarily obscure aspects of the microheat exchanging assembly.
Embodiments are directed to a microheat exchanging assembly and a ceramic assembly and methods of fabricating each. The microheat exchanging assembly is configured to cool one or more heat generating devices, such as electronic devices. In some embodiments, the microheat exchanging assembly includes a plurality of electrically and thermally conductive pads, each conductive pad is electrically isolated from each other. The heat generating device is electrically and thermally coupled to the conductive pad using any conventional method, such as soldering. In an exemplary application, each pad is coupled to one of an array of laser diodes used in high power lasers for industrial cutting and marking applications. In such an application, the microheat exchanging assembly is referred to a microheat exchanger for laser diodes (MELD™). The microheat exchanging assembly is particularly applicable to those applications requiring the arrangement of multiple heat generating devices in a common plane, such as a laser diode array. By electrically isolating each conductive pad, the heat generating devices coupled to the conductive pads are electrically isolated from each other while maintaining a uniform high rate of heat transfer from each heat generating device to a microheat exchanger. To provide this electrical isolation a ceramic layer with high thermal conductivity and high electrical resistivity is used. In some embodiments, the ceramic layer is made of beryllium oxide, aluminum oxide, or aluminum nitride. A top surface and a bottom surface of the ceramic layer are each bonded to a conductive layer using an intermediate joining material. Brazing of the joining material during the bonding process enables the liquidus joining material to melt, which provides a localized “flow” of material into the microvoids on the contact surfaces of the ceramic and conductive layers, thereby improving thermal efficiency. In some embodiments, each conductive layer is copper. The top conductive layer and the intermediate joining material are etched to form the electrically isolated conductive pads. The bonded ceramic and conductive layers form a first ceramic assembly.
The bottom conductive layer of the first ceramic assembly is bonded to a top surface of a microheat exchanger through which a cooling fluid circulates. The microheat exchanger is made of a thermally conductive material. In some embodiments, the microheat exchanger is made of copper. Heat is transferred from the heat generating devices coupled to the conductive pads to the fluid flowing through the microheat exchanger.
In some embodiments, a second ceramic assembly is formed and bonded to a bottom surface of the microheat exchanger. The second ceramic assembly can also include a plurality of electrically isolated conductive pads, which can be patterned the same or differently than those on the first ceramic assembly.
Fabrication of the microheat exchanging assembly includes the general steps of fabricating the ceramic assembly, fabricating the microheat exchanger, and final assembly and brazing of the microheat exchanging assembly.
A. Fabrication of the Ceramic Assembly
A ceramic assembly is formed by bonding a conductive layer to both sides of a thin ceramic plate using an intermediate joining material. In some embodiments, each conductive layer is a copper layer. In some embodiments, the ceramic plate is made of beryllium oxide (BeO), aluminum oxide (Al2O3), or aluminum nitride (AlN). The use of BeO may find restrictions due to its toxicity. Optimum thickness of the ceramic plate is dictated by the ability to minimize heat transfer resistance while maintaining mechanical strength of the bonded layer. The heat transfer resistance is reduced as the thickness of the ceramic plate is reduced, but the mechanical strength is increased as the thickness of the ceramic plate is increased. In some embodiments, the ceramic plate thickness varies from about 100 micrometers to several millimeters. In still other embodiments, the thickness of the ceramic plate is in the range of about 0.5 mm to about 0.75 mm. The thickness of each copper layer is dictated by the extent of warping of the assembled unit and the need for grinding the copper layer for its planarization. In some embodiments, the copper layer thickness is in the range of about 0.05 mm to about 0.5 mm. In still other embodiments, the thickness of the copper layer is about 0.25 mm. In some embodiments, the surface area of the ceramic assembly is in the range of about 1250 mm2 to about 8000 mm2.
A requirement of the fabrication of the ceramic assembly is to provide excellent bonding of the copper layers to the ceramic plate. Other than the ceramic plate, the remaining layers of the ceramic assembly are able to be patterned by selective removal of the copper layer and joining materials for making electrically isolated patterned copper pads. Various techniques for bonding copper to both sides of a ceramic plate are disclosed. One approach is the bare ceramic approach which uses active brazing alloy (ABA) materials such as copper-based ABA (Cu-ABA); copper and silver-based ABA (CuSil-ABA); and indium, copper, and silver-based ABA (InCuSil-ABA). Each of these ABAs is copper rich, and therefore provides good thermal conductivity. Each of these ABAs include a small amount of an active ingredient to bind with ceramic. In some embodiments, each of these ABAs includes titanium (Ti) as an active ingredient. Titanium in the ABA reacts with the ceramic plate and the copper layer to provide a chemical bond, resulting in a joining layer interface formed between the copper layer and the ceramic plate. It is understood that alternative ABAs including one or more active ingredients other than titanium can be used to bind with ceramic.
Further, the use of a brazing material as the intermediate joining material provides material “flow” into the microvoids of the contact surfaces. Brazing is a joining process whereby a joining material, such as a metal or alloy, is heated to a melting temperature. At the melting temperature, the liquidus joining material interacts with a thin layer of the base metal, cooling to form a strong, sealed joint. The resulting joining layer is a blend of the ABA material, the copper layer, and the ceramic layer. The melting temperature of the braze material is lower than the melting temperature of the materials being joined. Using the brazing process to bond the ceramic layer to the copper layer, the brazing temperature is lower than a conventional temperature used to direct copper bond the two layers together. Reducing the temperature also reduces the warping effects on the cooled copper-ceramic assembly.
Table 1 shows the composition and melting temperature of some selected active brazing alloys used in the copper and ceramic bonding process:
In some embodiments, each copper layer is a copper sheet and the ABA is used in a paste form. The ABA paste can be sprayed or screen printed on either both sides of the ceramic plate or on one side of each copper sheet that is to be attached to the ceramic plate.
In other embodiments, an ABA foil is placed between the ceramic plate and each copper sheet.
Another approach for bonding copper to both sides of a ceramic plate is the metallized ceramic approach which uses a high temperature refractory material including, but not limited to, molybdenum manganese (MoMn), titanium (Ti), or tungsten (W). In some embodiments, the refractory materials, such as MoMn paste, are screen printed onto each side of a ceramic plate. In other embodiments, the refractory materials, such as titanium or tungsten, are deposited by physical vapor deposition (PVD) onto a first side and a second side of a ceramic plate. The next step of metallization is to provide a thin layer coating of electrolytically or electrolessly deposited nickel, thereby forming a metallized ceramic plate. The nickel layer enables joining of the metallized ceramic plate to copper, or electroplating of copper directly onto the metallized ceramic plate. The metallized ceramic approach includes at least two options for bonding the metallized ceramic plate to copper.
A first option is the brazed copper option where a copper sheet is brazed to both sides of the metallized ceramic plate. In some embodiments, each copper sheet is plated with a thin layer of either silver or gold, which reacts with copper to form CuSil or CuAu, respectively, during bonding.
In other embodiments, a thin sheet of brazing alloy is placed between the metallized ceramic plate and each copper sheet. Examples of brazing alloy sheets include, but are not limited to, copper-silver-based sheets (CuSil sheets) or copper-gold-based sheets (CuAu sheets).
At the step 142, a brazing material is placed between the metallized ceramic layer and each of two copper sheets. In some embodiments, the brazing material is either silver or gold which is plated onto each copper sheet. In other embodiments, the brazing material is a brazing alloy sheet, such as a CuSil sheet or a CuAu sheet, which is positioned between the metallized ceramic plate and each of the copper sheets. In either case, each copper sheet is made of any conventional copper alloy including, but not limited to, 110, 102, or 101 copper. At a step 144, the copper sheet and brazing material are assembled on both sides of the metallized ceramic plate. At the step 146, the assembly from step 144 is vacuum brazed, thereby forming the ceramic assembly. In some embodiments, the brazing temperature of the step 146 is about 1510 degrees Fahrenheit.
A second option of the metallized ceramic approach for bonding the metallized ceramic plate to copper is the plated copper option which electroplates copper onto both sides of the metallized ceramic plate.
The ceramic assemblies formed by the above methods include a joining layer formed by bonding an intermediate joining material between each copper layer and the ceramic layer. The intermediate joining material provides a strong bonding of copper to the ceramic plate. The intermediate joining material is shown
The ceramic assembly described above provides a single device interface surface to which a heat generating device can be coupled. In some applications, multiple heat generating devices are to be coupled to the ceramic assembly. To accommodate multiple heat generating devices, a larger sized ceramic plate is used. In some embodiments, the width of the ceramic plate is about 50 mm and the length of the ceramic plate is about 160 mm. However, if the heat generating devices are coupled to the ceramic assembly with the single device interface surface, there is not electrical isolation between each of the coupled heat generating devices. Therefore, to provide electrical isolation between each of the multiple heat generating devices, electrically isolated copper pads are formed on one side of the ceramic assembly. To electrically isolate each pad, both the copper layer and the joining layer are etched to the ceramic layer. It is necessary to completely etch down to the ceramic layer to provide electrical isolation for each pad. If any joining material remains to connect the pads, electrical isolation is not achieved as the joining layer is electrically conductive.
Photopatterning includes selective removal of material through patterned photoresist and can be accomplished by wet etching or a combination of wet etching and physical methods of material removal, such as laser etching or bead blasting. The copper layer can be easily photopatterned using any conventional wet etch process. However, the joining layer is difficult to photopattern by wet etching. The joining layer can be wet etched but at the expense of over-etching the copper layer because copper is etched at a greater rate than the joining layer. A number of approaches are disclosed to pattern both the copper layer and the joining layer formed between the copper layer and the ceramic layer. The first approach uses a physical etch step. The physical etch step is any conventional physical method for removing material including, but not limited to, laser etching and bead blasting. The physical etch step is used either as part of a two step etching process or a single step etching process. In the two step etching process, a first wet etch step is performed to selectively etch the outer copper layer. A second physical etch step is then performed on the joining layer at the points exposed by the preceding wet etch performed on the copper layer. In the single etch step, a physical etch step is performed to simultaneously etch both the copper layer and the joining layer.
A second approach for patterning both the copper layer and the joining layer uses patterned screen printings to selectively apply the intermediate joining material on each side of the ceramic layer.
In
In
In
Using either the first approach, shown in
B. Fabrication of the Microheat Exchanger
The microheat exchanger is made of a thermally conductive material. In some embodiments, the microheat exchanger is made of copper. The microheat exchanger includes fluid pathways that enable fluid flow through the microheat exchanger. Heat is transferred from the thermally conductive material to fluid flowing through the microheat exchanger. The microheat exchanger includes one or more fluid input ports and one or more fluid output ports to enable fluid flow into and out of the microheat exchanger. In some embodiments, fluid pathways within the microheat exchanger are formed from cross hatched patterned fin design to provide flow uniformity either across the entire microheat exchanger or to select portions of the microheat exchanger. When the microheat exchanger is coupled to the ceramic assembly, the fluid pathways are designed to provide flow uniformity over the length of each heat generating device coupled to the conductive pads on the ceramic assembly. In some embodiments, the patterned fins are brazed to the microheat exchanger body using a CuSil sheet. In some embodiments, the thickness of the CuSil sheet is in the range of about 10 micrometer to about 100 micrometers. In still other embodiments, the thickness of the CuSil sheet is about 25 microns. It is understood that any conventional microheat exchanger that includes fluid flow therethrough can be used.
C. Fabrication of the Microheat Exchanging Assembly
Final assembly involves placing and aligning a first ceramic assembly, the microheat exchanger, and a second ceramic assembly in a fixture and brazing the fixed assembly in a vacuum or forming gas furnace. In some embodiments, only a single ceramic assembly is brazed to the microheat exchanger. A joining material is used to braze each ceramic assembly to the microheat exchanger. Where the microheat exchanger is made of copper and the bottom conducting layer of the ceramic assembly is also a copper layer, the joining material is a copper-to-copper joining material. In some embodiments, the joining material is a CuSil paste or CuSil foil. In an exemplary application, an eutectic CuSil joining material is made of 72% silver and 28% copper, having a melting temperature of 1435 degrees Fahrenheit. Using this CuSil joining material, a brazing temperature is about 1420 degrees Fahrenheit. Using a brazing process the joining material “flows” into the microvoids on the contact surfaces. Also, the brazing temperature and pressure for bonding the ceramic assembly to the microheat exchanger is lower than the brazing temperature and pressure used to fabricate the ceramic assembly. As such, using two separate fabrication steps, one to fabricate the ceramic assembly and another to fabricate the microheat exchanging assembly, does not put the microheat exchanger under as high a temperature or pressure, which reduces the chance of deformation. In other embodiments, the joining material is a solder paste or a solder foil. In general, any conventional metal-to-metal joining material can be used. In some embodiments, the thickness of the joining material is in the range of about 10 micrometer to about 100 micrometers. In still other embodiments, the thickness of the joining material is about 25 microns. In an alternative approach, instead of applying a separate joining material, the microheat exchanger body is plated with silver which forms CuSil during brazing. In some embodiments, the silver plating thickness is between about 1 micron and about 100 microns. In still other embodiments, the thickness of the silver plating is about 10 microns.
As describe above in the bare ceramic approach of fabricating the ceramic assembly, the ABA joining material can be applied as a foil or a paste. In some embodiments, the ABA joining material is Cu-ABA, CuSil-ABA, or InCuSil-ABA. In some embodiments, the joining material used for the joining layers 222 and 226 is a CuSil paste or a CuSil foil. In other embodiments, the joining material is a solder paste or a solder foil. In general, any conventional metal-to-metal joining material can be used.
As describe above in the brazed copper option of the metallized ceramic approach for fabricating the ceramic assembly, the metallized layer includes refractory materials, such as molybdenum manganese (MoMn), titanium (Ti), or tungsten (W), plated with nickel. The joining material used to form the joining layers 314, 322, 334, and 342 can be applied as a foil or a paste. In some embodiments, the joining material is a CuSil or CuAu paste or a CuSil or CuAu foil. In other embodiments, the joining material and copper layer are combined as a silver plated copper sheet. In some embodiments, the joining material used for the joining layers 326 and 330 is a CuSil paste or a CuSil foil. In other embodiments, the joining material is a solder paste or a solder foil. In general, any conventional metal-to-metal joining material can be used for the joining layers 326 and 330.
As describe above in the plated copper option of the metallized ceramic approach for fabricating the ceramic assembly, the metallized layer includes refractory materials, such as molybdenum manganese (MoMn), titanium (Ti), or tungsten (W), plated with nickel. The joining material can be applied as a foil or a paste. In some embodiments, the joining material is a CuSil or CuAu paste or a CuSil or a CuAu foil. In other embodiments, the joining material is a solder paste or a solder foil. In general, any conventional metal-to-metal joining material can be used for the joining layers 422 and 426.
The microheat exchanging assemblies are described above as bonding an outer surface of the ceramic assembly to an outer surface of the microheat exchanger via a joining material. In alternative embodiments, an intermediate layer, layers stack, block, or device, such as an additional microheat exchanger, can be positioned between the ceramic assembly and the microheat exchanger, where the intermediate layer, layers stack, block, or device is thermally conductive and includes outer surfaces conducive for bonding with the outer surface of the ceramic assembly and the outer surface of the microheat exchanger as described above.
The microheat exchanger has been described in terms of specific embodiments incorporating details to facilitate the understanding of the principles of construction and operation of the microheat exchanger. Such reference herein to specific embodiments and details thereof is not intended to limit the scope of the claims appended hereto. It will be apparent to those skilled in the art that modifications may be made in the embodiment chosen for illustration without departing from the spirit and scope of the microheat exchanger.
This application claims priority of U.S. provisional application, Ser. No. 61/188,078, filed Aug. 5, 2008, and entitled “Fabrication of Microheat Exchanger for Laser Diode Cooling”, by these same inventors. This application incorporates U.S. provisional application, Ser. No. 61/188,078 in its entirety by reference.
Number | Name | Date | Kind |
---|---|---|---|
596062 | Firey | Dec 1897 | A |
2039593 | Hubbuch et al. | May 1936 | A |
2087521 | Mazzola | Jul 1937 | A |
2273505 | Florian | Feb 1942 | A |
2956642 | Chaplin et al. | Oct 1960 | A |
3220254 | Halbech | Nov 1965 | A |
3361195 | Meyerhoff et al. | Jan 1968 | A |
3491184 | Rietdijk | Jan 1970 | A |
3514967 | Vander Molen | Jun 1970 | A |
3654988 | Clayton, III | Apr 1972 | A |
3771219 | Tuzi et al. | Nov 1973 | A |
3817321 | Von Cube et al. | Jun 1974 | A |
3823572 | Cochran, Jr. | Jul 1974 | A |
3852806 | Corman et al. | Dec 1974 | A |
3929154 | Goodwin | Dec 1975 | A |
3946276 | Braun et al. | Mar 1976 | A |
3948316 | Souriau | Apr 1976 | A |
3993123 | Chu et al. | Nov 1976 | A |
4021867 | Maxwell, Jr. | May 1977 | A |
4037889 | Piatt | Jul 1977 | A |
RE29513 | Johnson | Jan 1978 | E |
4109707 | Wilson et al. | Aug 1978 | A |
4138996 | Cartland | Feb 1979 | A |
4194559 | Eastman | Mar 1980 | A |
4203488 | Johnson et al. | May 1980 | A |
4211208 | Lindner | Jul 1980 | A |
4235285 | Johnson et al. | Nov 1980 | A |
4248295 | Ernst et al. | Feb 1981 | A |
4262975 | Heshmat et al. | Apr 1981 | A |
4312012 | Fresieret et al. | Jan 1982 | A |
4332291 | Mulock-Bentley | Jun 1982 | A |
4345267 | Corman et al. | Aug 1982 | A |
4395947 | Despot | Aug 1983 | A |
4409079 | Miyazaki et al. | Oct 1983 | A |
4416324 | Sutoh et al. | Nov 1983 | A |
4450472 | Tuckerman et al. | May 1984 | A |
4467861 | Kiseev et al. | Aug 1984 | A |
4485429 | Mittal | Nov 1984 | A |
4494171 | Bland et al. | Jan 1985 | A |
4497875 | Arakawa et al. | Feb 1985 | A |
4516632 | Swift et al. | May 1985 | A |
4540115 | Hawrylo | Sep 1985 | A |
4561040 | Eastman et al. | Dec 1985 | A |
4567505 | Pease et al. | Jan 1986 | A |
4573067 | Tuckerman et al. | Feb 1986 | A |
4574876 | Aid | Mar 1986 | A |
4644385 | Nakanishi et al. | Feb 1987 | A |
4664181 | Sumberg | May 1987 | A |
4675783 | Murase | Jun 1987 | A |
4687167 | Skalka et al. | Aug 1987 | A |
4716494 | Bright et al. | Dec 1987 | A |
4758926 | Herrell et al. | Jul 1988 | A |
4793405 | Diggelmann et al. | Dec 1988 | A |
4866570 | Porter | Sep 1989 | A |
4868712 | Woodman | Sep 1989 | A |
4893174 | Yamada et al. | Jan 1990 | A |
4894709 | Phillips et al. | Jan 1990 | A |
4896719 | O'Neill et al. | Jan 1990 | A |
4908112 | Pace | Mar 1990 | A |
4938280 | Clark | Jul 1990 | A |
4978638 | Buller et al. | Dec 1990 | A |
5009760 | Zare et al. | Apr 1991 | A |
5016090 | Galyon et al. | May 1991 | A |
5016138 | Woodman | May 1991 | A |
5016707 | Nguyen | May 1991 | A |
5027611 | Doi et al. | Jul 1991 | A |
5036676 | Dudley | Aug 1991 | A |
5043797 | Lopes | Aug 1991 | A |
5057908 | Weber | Oct 1991 | A |
5058627 | Brannen | Oct 1991 | A |
5070040 | Pankove | Dec 1991 | A |
5083194 | Bartilson | Jan 1992 | A |
5088005 | Ciaccio | Feb 1992 | A |
5099311 | Bonde et al. | Mar 1992 | A |
5099910 | Walpole et al. | Mar 1992 | A |
5105430 | Mundinger et al. | Apr 1992 | A |
5125451 | Matthews | Jun 1992 | A |
5131233 | Cray et al. | Jul 1992 | A |
5142970 | ErkenBrack | Sep 1992 | A |
5145001 | Valenzuela | Sep 1992 | A |
5161089 | Chu et al. | Nov 1992 | A |
5199487 | DiFrancesco et al. | Apr 1993 | A |
5203401 | Hamburgen et al. | Apr 1993 | A |
5218515 | Bernhardt | Jun 1993 | A |
5228502 | Chu et al. | Jul 1993 | A |
5232047 | Matthews | Aug 1993 | A |
5239200 | Messina et al. | Aug 1993 | A |
5239443 | Fahey et al. | Aug 1993 | A |
5263251 | Matthews | Nov 1993 | A |
5265670 | Zingher | Nov 1993 | A |
5269372 | Chu et al. | Dec 1993 | A |
5275237 | Rolfson et al. | Jan 1994 | A |
5294834 | Fatemi et al. | Mar 1994 | A |
5299635 | Abraham | Apr 1994 | A |
5308429 | Bradley | May 1994 | A |
5309319 | Messina | May 1994 | A |
5310440 | Zingher | May 1994 | A |
5316077 | Reichard | May 1994 | A |
5317805 | Hoopman et al. | Jun 1994 | A |
5325265 | Turlik et al. | Jun 1994 | A |
5346000 | Schlitt | Sep 1994 | A |
5380956 | Loo et al. | Jan 1995 | A |
5383340 | Larson et al. | Jan 1995 | A |
5386143 | Fitch | Jan 1995 | A |
5388635 | Gruber et al. | Feb 1995 | A |
5397919 | Tata et al. | Mar 1995 | A |
5421943 | Tam et al. | Jun 1995 | A |
5427174 | Lomolino, Sr. et al. | Jun 1995 | A |
5436793 | Sanwo et al. | Jul 1995 | A |
5459099 | Hsu | Oct 1995 | A |
5488835 | Howenstine et al. | Feb 1996 | A |
5490117 | Oda et al. | Feb 1996 | A |
5508234 | Dusablon, Sr. et al. | Apr 1996 | A |
5514832 | Dusablon, Sr. et al. | May 1996 | A |
5514906 | Love et al. | May 1996 | A |
5520244 | Mundinger et al. | May 1996 | A |
5544696 | Leland | Aug 1996 | A |
5548605 | Bennett et al. | Aug 1996 | A |
5564497 | Fukuoka et al. | Oct 1996 | A |
5575929 | Yu et al. | Nov 1996 | A |
5579828 | Reed et al. | Dec 1996 | A |
5585069 | Zanzucchi et al. | Dec 1996 | A |
5622221 | Genga, Jr. et al. | Apr 1997 | A |
5641400 | Kaltenbach et al. | Jun 1997 | A |
5647429 | Oktay et al. | Jul 1997 | A |
5651414 | Susuki et al. | Jul 1997 | A |
5658831 | Layton et al. | Aug 1997 | A |
5672980 | Charlton et al. | Sep 1997 | A |
5675473 | McDunn et al. | Oct 1997 | A |
5676198 | Schneider et al. | Oct 1997 | A |
5692558 | Hamilton et al. | Dec 1997 | A |
5696405 | Weld | Dec 1997 | A |
5703536 | Davis et al. | Dec 1997 | A |
5704416 | Larson et al. | Jan 1998 | A |
5718628 | Nakazato et al. | Feb 1998 | A |
5727618 | Mundinger et al. | Mar 1998 | A |
5731954 | Cheon | Mar 1998 | A |
5757070 | Fritz | May 1998 | A |
5763951 | Hamilton et al. | Jun 1998 | A |
5768104 | Salmonson et al. | Jun 1998 | A |
5774779 | Tuchinskiy | Jun 1998 | A |
5800690 | Chow et al. | Sep 1998 | A |
5801442 | Hamilton et al. | Sep 1998 | A |
5810077 | Nakamura et al. | Sep 1998 | A |
5811062 | Wegeng et al. | Sep 1998 | A |
5835345 | Staskus et al. | Nov 1998 | A |
5836750 | Cabuz | Nov 1998 | A |
5847452 | Tantoush | Dec 1998 | A |
5858188 | Soane et al. | Jan 1999 | A |
5863708 | Zanzucchi et al. | Jan 1999 | A |
5869004 | Parce et al. | Feb 1999 | A |
5870823 | Bexama et al. | Feb 1999 | A |
5874795 | Sakamoto | Feb 1999 | A |
5876655 | Fisher | Mar 1999 | A |
5880017 | Schwiebert et al. | Mar 1999 | A |
5880524 | Xie | Mar 1999 | A |
5882248 | Wright et al. | Mar 1999 | A |
5886870 | Omori | Mar 1999 | A |
5887557 | Battlogg | Mar 1999 | A |
5896869 | Maniscalco et al. | Apr 1999 | A |
5898572 | Schennib et al. | Apr 1999 | A |
5901037 | Hamilton et al. | May 1999 | A |
5909057 | McCormick et al. | Jun 1999 | A |
5927390 | Lehman | Jul 1999 | A |
5936192 | Tauchi | Aug 1999 | A |
5940270 | Puckett | Aug 1999 | A |
5942093 | Rakestraw et al. | Aug 1999 | A |
5945217 | Hanrahan | Aug 1999 | A |
5957194 | Azar | Sep 1999 | A |
5960866 | Kimura et al. | Oct 1999 | A |
5963887 | Giorgio | Oct 1999 | A |
5964092 | Tozuka et al. | Oct 1999 | A |
5965001 | Chow et al. | Oct 1999 | A |
5965813 | Wan et al. | Oct 1999 | A |
5978220 | Frey et al. | Nov 1999 | A |
5997713 | Beetz, Jr. et al. | Dec 1999 | A |
5998240 | Hamilton et al. | Dec 1999 | A |
6007309 | Hartley | Dec 1999 | A |
6010316 | Haller et al. | Jan 2000 | A |
6013164 | Paul et al. | Jan 2000 | A |
6014312 | Schulz-Harder et al. | Jan 2000 | A |
6019165 | Batchelder | Feb 2000 | A |
6019882 | Paul et al. | Feb 2000 | A |
6021045 | Johnson | Feb 2000 | A |
6031751 | Janko | Feb 2000 | A |
6034872 | Chrysler et al. | Mar 2000 | A |
6039114 | Becker et al. | Mar 2000 | A |
6054034 | Soane et al. | Apr 2000 | A |
6058014 | Choudhury et al. | May 2000 | A |
6068752 | Dubrow et al. | May 2000 | A |
6069791 | Goto et al. | May 2000 | A |
6084178 | Cromwell | Jul 2000 | A |
6086330 | Press et al. | Jul 2000 | A |
6090251 | Sundberg et al. | Jul 2000 | A |
6096656 | Matzke et al. | Aug 2000 | A |
6100541 | Nagle et al. | Aug 2000 | A |
6101715 | Fuesser et al. | Aug 2000 | A |
6105373 | Watanabe et al. | Aug 2000 | A |
6119729 | Oberholzer | Sep 2000 | A |
6126723 | Drost et al. | Oct 2000 | A |
6129145 | Yamamoto et al. | Oct 2000 | A |
6129260 | Andrus et al. | Oct 2000 | A |
6131650 | North et al. | Oct 2000 | A |
6140860 | Sandhu et al. | Oct 2000 | A |
6146103 | Lee et al. | Nov 2000 | A |
6154363 | Chang | Nov 2000 | A |
6159353 | West et al. | Dec 2000 | A |
6166907 | Chien | Dec 2000 | A |
6167948 | Thomas | Jan 2001 | B1 |
6174675 | Chow et al. | Jan 2001 | B1 |
6176962 | Soane et al. | Jan 2001 | B1 |
6186660 | Kopf-Sill et al. | Feb 2001 | B1 |
6196307 | Ozmat | Mar 2001 | B1 |
6206022 | Tsai et al. | Mar 2001 | B1 |
6216343 | Leland et al. | Apr 2001 | B1 |
6221226 | Kopf-Sill | Apr 2001 | B1 |
6227257 | Griffiths | May 2001 | B1 |
6227287 | Tanaka et al. | May 2001 | B1 |
6227809 | Forster et al. | May 2001 | B1 |
6234240 | Cheon | May 2001 | B1 |
6238538 | Parce et al. | May 2001 | B1 |
6253832 | Hallefalt | Jul 2001 | B1 |
6253835 | Chu et al. | Jul 2001 | B1 |
6253836 | Mitchell | Jul 2001 | B1 |
6257320 | Wargo | Jul 2001 | B1 |
6301109 | Chu et al. | Oct 2001 | B1 |
6313992 | Hildebrandt | Nov 2001 | B1 |
6317326 | Vogel et al. | Nov 2001 | B1 |
6321791 | Chow | Nov 2001 | B1 |
6322753 | Lindberg et al. | Nov 2001 | B1 |
6324058 | Hsaio | Nov 2001 | B1 |
6324075 | Unrein et al. | Nov 2001 | B1 |
6337794 | Agonafer et al. | Jan 2002 | B1 |
6351384 | Darkoku et al. | Feb 2002 | B1 |
6355505 | Maeda et al. | Mar 2002 | B1 |
6360814 | Tanaka et al. | Mar 2002 | B1 |
6362958 | Yu et al. | Mar 2002 | B1 |
6366462 | Chu et al. | Apr 2002 | B1 |
6366467 | Patel et al. | Apr 2002 | B1 |
6367544 | Calaman | Apr 2002 | B1 |
6381813 | Lai | May 2002 | B1 |
6388317 | Reese | May 2002 | B1 |
6396706 | Wohlfarth | May 2002 | B1 |
6397932 | Calaman et al. | Jun 2002 | B1 |
6400012 | Miller et al. | Jun 2002 | B1 |
6406605 | Moles | Jun 2002 | B1 |
6415860 | Kelly et al. | Jul 2002 | B1 |
6417060 | Tavkhelidze et al. | Jul 2002 | B2 |
6424531 | Bhatti et al. | Jul 2002 | B1 |
6492018 | Guddal | Dec 2002 | B1 |
6493221 | Harrison et al. | Dec 2002 | B2 |
6533840 | Martin et al. | Mar 2003 | B2 |
6639799 | Prasher et al. | Oct 2003 | B2 |
6651452 | Lecke et al. | Nov 2003 | B2 |
6657860 | Matsui et al. | Dec 2003 | B2 |
6679315 | Cosley et al. | Jan 2004 | B2 |
6680044 | Tonkovich et al. | Jan 2004 | B1 |
6729383 | Cannell et al. | May 2004 | B1 |
6743664 | Liang et al. | Jun 2004 | B2 |
6775137 | Chu et al. | Aug 2004 | B2 |
6775996 | Cowans | Aug 2004 | B2 |
6787052 | Vaganov | Sep 2004 | B1 |
6787899 | Rinella et al. | Sep 2004 | B2 |
6796372 | Bear | Sep 2004 | B2 |
6807056 | Kondo et al. | Oct 2004 | B2 |
6819563 | Chu et al. | Nov 2004 | B1 |
6863117 | Valenzuela | Mar 2005 | B2 |
6881039 | Corbin et al. | Apr 2005 | B2 |
6882543 | Kenny, Jr. et al. | Apr 2005 | B2 |
6896612 | Novotny | May 2005 | B1 |
6914779 | Askeland et al. | Jul 2005 | B2 |
6924981 | Chu et al. | Aug 2005 | B2 |
6945324 | Weng | Sep 2005 | B2 |
6955212 | Hsieh | Oct 2005 | B1 |
6973801 | Campbell et al. | Dec 2005 | B1 |
6986382 | Upadhya et al. | Jan 2006 | B2 |
6988534 | Kenny et al. | Jan 2006 | B2 |
6988535 | Upadhya et al. | Jan 2006 | B2 |
6994151 | Zhou et al. | Feb 2006 | B2 |
7000684 | Kenny et al. | Feb 2006 | B2 |
7017654 | Kenny et al. | Mar 2006 | B2 |
7019972 | Kenny, Jr. et al. | Mar 2006 | B2 |
7021369 | Werner et al. | Apr 2006 | B2 |
7044196 | Shook et al. | May 2006 | B2 |
7050308 | Kenny, Jr. et al. | May 2006 | B2 |
7051802 | Baer | May 2006 | B2 |
7061104 | Kenny, Jr. et al. | Jun 2006 | B2 |
7077634 | Munch et al. | Jul 2006 | B2 |
7086839 | Kenny et al. | Aug 2006 | B2 |
7090001 | Zhou et al. | Aug 2006 | B2 |
7104312 | Goodson et al. | Sep 2006 | B2 |
7143816 | Ghosh et al. | Dec 2006 | B1 |
7156159 | Lovette et al. | Jan 2007 | B2 |
7178512 | Merten | Feb 2007 | B1 |
7188662 | Brewer et al. | Mar 2007 | B2 |
7190583 | Fendley et al. | Mar 2007 | B1 |
7201012 | Munch et al. | Apr 2007 | B2 |
7201214 | Munch et al. | Apr 2007 | B2 |
7221858 | Ku | May 2007 | B2 |
7233494 | Campbell et al. | Jun 2007 | B2 |
7278549 | Munch et al. | Oct 2007 | B2 |
7293423 | Upadhya et al. | Nov 2007 | B2 |
7295444 | Wang | Nov 2007 | B1 |
7301773 | Brewer et al. | Nov 2007 | B2 |
7342789 | Hall et al. | Mar 2008 | B2 |
7344363 | Munch et al. | Mar 2008 | B2 |
7385810 | Chu et al. | Jun 2008 | B2 |
7398821 | Rainer et al. | Jul 2008 | B2 |
7402029 | Munch et al. | Jul 2008 | B2 |
7430118 | Noteboom et al. | Sep 2008 | B1 |
7434412 | Miyahira et al. | Oct 2008 | B1 |
7449122 | Corbin et al. | Nov 2008 | B2 |
7455103 | Sato et al. | Nov 2008 | B2 |
7462852 | Appleby et al. | Dec 2008 | B2 |
7591302 | Lenehan et al. | Sep 2009 | B1 |
7666215 | Callister et al. | Feb 2010 | B2 |
20020011330 | Insley et al. | Jan 2002 | A1 |
20020075645 | Kitano et al. | Jun 2002 | A1 |
20020080578 | Xie | Jun 2002 | A1 |
20030077474 | Rabinkin et al. | Apr 2003 | A1 |
20030205363 | Chu et al. | Nov 2003 | A1 |
20040008483 | Cheon | Jan 2004 | A1 |
20040012927 | Lee et al. | Jan 2004 | A1 |
20040050538 | Sunder et al. | Mar 2004 | A1 |
20040105234 | Messina et al. | Jun 2004 | A1 |
20040188059 | Todd, Jr. et al. | Sep 2004 | A1 |
20040188076 | Lee | Sep 2004 | A1 |
20040206477 | Kenny et al. | Oct 2004 | A1 |
20040216863 | Hu | Nov 2004 | A1 |
20040221603 | Arik et al. | Nov 2004 | A1 |
20040221604 | Ota et al. | Nov 2004 | A1 |
20040228091 | Miyairi | Nov 2004 | A1 |
20050024832 | Lee et al. | Feb 2005 | A1 |
20050029242 | Bonnet et al. | Feb 2005 | A1 |
20050041393 | Tustaniwski et al. | Feb 2005 | A1 |
20050061013 | Bond | Mar 2005 | A1 |
20050133200 | Malone et al. | Jun 2005 | A1 |
20050174737 | Meir | Aug 2005 | A1 |
20050247433 | Corrado et al. | Nov 2005 | A1 |
20050259393 | Vinson et al. | Nov 2005 | A1 |
20060037739 | Utsunomiya | Feb 2006 | A1 |
20060120039 | Yuval | Jun 2006 | A1 |
20060139882 | Mikubo et al. | Jun 2006 | A1 |
20060171113 | Wu | Aug 2006 | A1 |
20060187639 | Carswell | Aug 2006 | A1 |
20060232945 | Chu et al. | Oct 2006 | A1 |
20060245987 | Schmidt | Nov 2006 | A1 |
20070006460 | Kim | Jan 2007 | A1 |
20070039719 | Eriksen | Feb 2007 | A1 |
20070042514 | Wu et al. | Feb 2007 | A1 |
20070053161 | Giardina et al. | Mar 2007 | A1 |
20070098143 | Thankgamani et al. | May 2007 | A1 |
20070109739 | Stefanoski | May 2007 | A1 |
20070152352 | McKinnell et al. | Jul 2007 | A1 |
20070164088 | Dianatkhah | Jul 2007 | A1 |
20070211428 | Doll, Jr. | Sep 2007 | A1 |
20070227708 | Hom et al. | Oct 2007 | A1 |
20070235167 | Brewer et al. | Oct 2007 | A1 |
20070266714 | Fielder | Nov 2007 | A1 |
20070267181 | Lin et al. | Nov 2007 | A1 |
20070297136 | Konshak | Dec 2007 | A1 |
20080023180 | Bunker et al. | Jan 2008 | A1 |
20080024992 | Pflueger | Jan 2008 | A1 |
20080110963 | Lin et al. | May 2008 | A1 |
20080285228 | Koch et al. | Nov 2008 | A1 |
20090159241 | Lipp et al. | Jun 2009 | A1 |
20090183520 | Yukimoto | Jul 2009 | A1 |
20090225513 | Correa et al. | Sep 2009 | A1 |
20090262495 | Neudorfer | Oct 2009 | A1 |
20100132640 | Methley et al. | Jun 2010 | A1 |
20110073292 | Datta et al. | Mar 2011 | A1 |
Number | Date | Country |
---|---|---|
3314069 | Dec 1983 | DE |
3927755 | Feb 1991 | DE |
19628548 | Jan 1998 | DE |
29717480 | Feb 1998 | DE |
197 15 001 | Dec 1998 | DE |
69413012 | Mar 1999 | DE |
69511875 | Mar 2000 | DE |
10141525 | Mar 2003 | DE |
102004042154 | Mar 2006 | DE |
0 520 173 | Dec 1992 | EP |
0720720 | Jan 1998 | EP |
0845728 | Mar 1998 | EP |
1 003 006 | May 2000 | EP |
60046056 | Dec 1985 | JP |
2005080901 | Sep 2005 | WO |
WO 2005080901 | Sep 2005 | WO |
2007006590 | Jan 2007 | WO |
Number | Date | Country | |
---|---|---|---|
20100032143 A1 | Feb 2010 | US |
Number | Date | Country | |
---|---|---|---|
61188078 | Aug 2008 | US |