This application claims the benefit under 35 USC §119(e) of U.S. provisional application Ser. No. 60/719,110 filed Sep. 22, 2005.
1. Field of the Invention
This invention relates to mechanical devices that have a component in which large recoverable distortions are available in non-extruded shapes.
2. Description of the Related Art
Common shape memory alloy (also called SMA) materials such as Nitinol can be shape-set by heating to an annealing temperature while constrained to a shape, and then cooling. For example, a helix may be formed from a straight TiNi wire by winding the wire on a mandrel, securing the ends, heating to 550 deg. C., and cooling. The rates of heating and cooling are not critical in this ‘shape-setting’ process for TiNi, although special characteristics are achieved by holding the temperature constant at specific temperatures.
It is a general object of the invention to provide methods for methods for the shape setting fabrication of single crystal shape memory alloys (also called “hyperelastic”), such as CuAlNi and to provide devices made by such methods.
A further object of this invention is to provide new and improved devices made of hyperelastic single crystal SMA by novel methods of shape-setting.
Hyperelastic alloys formed as single crystals of approximately Cu(84)Al(14)Ni(4) wt. % have enhanced strain recovery properties compared to more conventional polycrystal SMAs such as Nitinol. Such single crystals are formed as extruded shapes whether by pulling from melt or by continuous casting. It is desirable to form other shapes such as helices or bends, but the methodology used for forming Nitinol destroys the single crystallinity; a problem with polycrystal CuAlNi is that it is brittle. Therefore there is a need for methods which avoid these and other problems.
The fabrication and performance of such single crystal SMA materials are disclosed in U.S. application Ser. No. 10/588,412 filed Jul. 31, 2006, the disclosure of which is incorporated by this reference.
Single-crystal CuAlNi is drawn from melt and cooled by use of the Stepanov method. As the single crystal cools, precipitates form so that strength, shape memory, and hyperelastic properties are not optimal. Imparting shape memory and hyperelastic properties requires heating to a temperature high enough to dissolve the precipitates, followed immediately by rapid cooling (“quenching”) to lock in the dissolved elemental components. Methods used for producing single crystal shape memory alloys generally produce net shapes in the crystal.
Use of elevated temperature to modify the shape of hyperelastic single crystal of CuAlNi normally results in loss of single crystallinity: at elevated temperatures precipitation of elemental components (especially Al) changes the composition. For this reason actuators and flexures designed to exploit the extraordinary strain recovery of these materials (9% strain) have been limited to net shapes (solid and tubular cylinders) produced during formation of the crystal. However, if heating and quenching take place in a very short time (fraction of a second) the precipitation does not progress far enough to cause significant change in the composition and the hyperelastic properties can be retained. These discoveries by the present inventors enable a variety of methods for shape-setting single crystal SMAs. Extruded shapes may be bent, elongated with reduction of diameter, and tubular as well as solid crystal shapes may be re-formed. These novel methods extend the usefulness of single crystal SMA by removing a limitation on shapes.
Single crystals pulled from melt have an as-formed or extruded shape such as a solid or hollow cylindrical shape with a constant cross-sectional form. It is sometimes advantageous to alter the fabricated shape into a shape more suited to a particular application. One such application is for use as eyeglass frame hinge flexures to replace hinges or to replace the entire eyeglass frame. Another is to form curves in a guidewire to follow tortuous path in a blood vessel, or a sieve placed in a blood vessel for the purpose of retrieving and removing a blood clot. The various embodiments of the present invention provides processes for “shape-setting” CuAlNi or other single-crystal materials.
CuAlNi single crystal is in a metastable condition and gradually deteriorates to polycrystalline form. The rate of decomposition is temperature dependent. At room temperature the rate is sufficiently low that negligible change takes place over years. At 300-400 deg. C. the rate is rapid enough that degeneration to multiple crystals may occur in a few seconds. Once formed, the multiple crystals do not re-form as a single crystal: this requires melting and special processing. However, CuAlNi may retain its single crystal condition through repeated heating to annealing temperature and rapid cooling. At sufficiently high temperature (typically 850-950 deg. C.) the three components Cu, Al, and Ni are in solution. CuAlNi's hyperelastic properties are exhibited within a very narrow range of compositions. If cooling is not sufficiently rapid, Al precipitates form, changing the composition and drastically altering thermo-mechanical properties.
The crucial insight leading to the present invention is that a combination of annealing, constrained shaping, and quenching leads to an altered “remembered” shape.
Quenching, that is rapidly lowering the temperature from a temperature at which the three components Cu, Al, and Ni are in solution, is conventionally used to “freeze in” the composition by not permitting elemental components from forming precipitates. If cooling takes place slowly these precipitates remove atoms from the crystal lattice and modify it in such a way as to destroy the phase transformation that leads to the shape memory effect. Rapid cooling preserves the integrity of the solution.
Composition can be altered during heating and cooling cycles by the fact that Al at the surface forms aluminum oxide, and the oxide, being insoluble, is effectively removed from the material. Reducing the Al content by 0.1%, which increases the phase transformation temperature, may alter the transition point enough to make the material useless.
It is a common characteristic of metals that there is a temperature range below the melting point within which internal stresses are minimal. Such an ‘annealed’ material can be deformed far beyond its natural limits without breaking, and the deformed shape is retained after cooling.
The annealing temperature of CuAlNi single crystal alloy is about 600 deg. C. When heated to this temperature its shape may be drastically changed with very small applied forces. When cooled, the material retains the modified shape, and if it is rapidly cooled it also retains its shape memory qualities.
To shape-set a portion of elongated component of CuAlNi it is important that heating and cooling both be very rapid. Otherwise the material in the heat-affected zone adjacent to the heated portion may undergo precipitation, resulting in an altered composition, or it may form multiple crystals because of critical stress. Polycrystalline alloys have far less strain tolerance and recovery, so are much inferior in performance compared to single crystals.
If the objective is to make a bend in, for example, a wire, then it is necessary either to heat all of the wire uniformly or the heating and cooling must be done quickly.
Otherwise the wire in the heat-affected zone between the heated segment and the un-heated segment will be held at an intermediate temperature, above ambient but below the annealing temperature. In this intermediate temperature range the CuAlNi single crystal is unstable and will degenerate rapidly to polycrystal form and be quite brittle.
Rapid cooling is satisfactorily performed by submersion in salt water. Rapid heating is not as readily accomplished. Several methods are demonstrable: each has advantages and disadvantages.
Rapid heating can be accomplished by immersing the object to be shape-set in a very hot flame such as provided by an oxy-acetylene torch. The sample is held in the flame while it transforms and becomes straight, begins to glow, and then anneals. The sample is then quickly removed from the flame and, while constrained in the desired shape, it is plunged into salt water. Salt water is used because a layer of bubbles does not form to insulate the surface of the material.
Another method is to constrain the shape of the wire to the desired shape in a mold, heat the mold, and quench. Quench must be relatively fast, but in this case the specimen may be held at an elevated temperature (850-950 deg. C.) for as long as is convenient.
For example, a CuAlNi wire is inserted in a stainless steel tube. The tube is heated to its annealing temperature (about 850 deg. C.) and shaped by bending. Several bends may be incorporated. After bending, the tube is uniformly heated in an oven to 650-750 deg. C. to anneal the CuAlNi, then quickly quenched. The CuAlNi wire when removed from the stainless steel tube retains the modified shape: it has been shape-set.
A variation of this method is first to form a stainless steel tube into the shape desired, for example by heating segments in an acetylene flame and bending. After the tube is formed the CuAlNi wire is inserted into it at room temperature, and the tube with wire inside are heated and quenched. In this case it is important not to deform the CuAlNi too much as it may form multiple crystals. Re-crystallization occurs rapidly if CuAlNi is overstressed.
CuAlNi contained within a stainless steel tube is not ideal for rapid cooling. Cooling rate may be significantly enhanced by forming a number of holes in the tube to allow contact with the water and to reduce the insulating effect of air trapped within the tube.
Samples of hyperelastic CuAlNi heated to 950 deg. C. in stainless steel tube and cooled by immersion in salt water have been found to be martensitic although shape-setting has taken place. The transition temperature may be reduced by re-heating the sample without the stainless steel mold and quenching it bare.
If deformation takes place prior to heating, strain must be limited to the plateau, about 9%, so as not to re-crystallize. If the sample is heated to near melting, then deformed and quenched, much larger deformations are tolerated.
Stainless steel is used to constrain the deformed hyperelastic wire because the annealing temperature of stainless steel is higher than the temperature at which CuAlNi softens and becomes easily deformed. During heating, as the plateau stress of the hyperelastic material increases, the hyperelastic material exerts a great force. If a copper tube is used, its walls must be thick compared to the diameter of the hyperelastic. Otherwise, the force of the hyperelastic material shape recovery may cause the Cu tube to (partially) straighten because Cu anneals at a temperature lower than the softening temperature of hyperelastic material.
Another method is to heat the material by a laser beam or by an infrared heater. The beam may be moved onto the sample or vice versa. The technique works better if two beams are used, one on each surface. Quenching may be by spraying or dousing with salt water or other heat absorber.
Another method of rapid heating is by joule heating. A pulse of electrical energy is directed such that it is dissipated in the material, heating it to near incandescence. If heating is very rapid the material may be immersed during the heating phase, so that at the end of the joule heating pulse it immediately cools. Otherwise the sample may be moved so that it is immersed, or doused or sprayed with cold liquid.
The joule heating method is not limited to materials of small diameter. However, it is difficult to deliver the electrical energy into the CuAlNi as it is a very good electrical conductor (resistivity is of the order of 30 microhm cm. Pure copper is 1.5 microhm cm.)
Still another method of heating is by induction heating.
These methods work best on material samples that are small in one dimension such as thin foils or fine wires.
A 1 mm diameter CuAlNi straight hyperelastic wire having a transition temperature at +10 deg. C was held in a curved shape with two pairs of pliers while being placed in an oxy-acetylene flame for approximately 3 seconds. The wire stiffened and straightened as it was heated, then softened and bent to a radius of about 5 mm. It was rapidly cooled by immersion in a pan of room-temperature salt water. After this procedure the wire retained a curvature of about 5 mm under no external stress, and returned to this shape after being straightened. This degree of curvature corresponds to a strain of approximately 10%, which compares favorably with the hyperelastic properties of the untreated wire, but with an altered shape.
One appropriate application is as a flexure to replace hinges in eyeglasses. A strip of CuAlNi is shape-set so that it is bent at a right angle. One end is attached to the frame, the other is attached to the temple piece of the glasses. A cam or eccentric may be included to provide two stable positions: with the glasses worn on the face, or with the glasses folded for transport or storage. Alternatively the entire glasses frame may be fabricated of CuAlNi single crystal wire by appropriate shape-setting.
As shown in
Number | Name | Date | Kind |
---|---|---|---|
368425 | Ross et al. | Aug 1887 | A |
538593 | Naylor, Jr. | Apr 1895 | A |
1560335 | Czochralski | Nov 1925 | A |
1904828 | Green | Apr 1933 | A |
1913035 | Loepsinger | Jun 1933 | A |
1926925 | Wescott | Sep 1933 | A |
2060593 | Schaurte et al. | Nov 1936 | A |
2371614 | Graves | Mar 1945 | A |
2586556 | Mullikin | Feb 1952 | A |
2608996 | Forman | Sep 1952 | A |
2610300 | Walton et al. | Sep 1952 | A |
2647017 | Coulliette | Jul 1953 | A |
2911504 | Cohn | Nov 1959 | A |
3229956 | White | Jan 1966 | A |
3351463 | Rozner et al. | Nov 1967 | A |
3357432 | Sparks | Dec 1967 | A |
3400906 | Stocklin | Sep 1968 | A |
3408890 | Bochman, Jr. | Nov 1968 | A |
3435823 | Edwards | Apr 1969 | A |
3445086 | Quinn | May 1969 | A |
3454286 | Anderson et al. | Jul 1969 | A |
3546996 | Grijalva et al. | Dec 1970 | A |
3559641 | Lay | Feb 1971 | A |
3561537 | Dix et al. | Feb 1971 | A |
3613732 | Willson et al. | Oct 1971 | A |
3620212 | Fannon, Jr. et al. | Nov 1971 | A |
3659625 | Coiner et al. | May 1972 | A |
3725835 | Hopkins et al. | Apr 1973 | A |
3789838 | Fournier et al. | Feb 1974 | A |
3849756 | Hickling | Nov 1974 | A |
3888975 | Ramwell | Jun 1975 | A |
3913572 | Wheeler | Oct 1975 | A |
3918443 | Vennard et al. | Nov 1975 | A |
3974844 | Pimentel | Aug 1976 | A |
4055955 | Johnson | Nov 1977 | A |
4063831 | Meuret | Dec 1977 | A |
4072159 | Kurosawa | Feb 1978 | A |
4096993 | Behr | Jun 1978 | A |
4151064 | Kuehnle | Apr 1979 | A |
4176719 | Bray | Dec 1979 | A |
4177327 | Mathews | Dec 1979 | A |
4195773 | Ogden | Apr 1980 | A |
4243963 | Jameel et al. | Jan 1981 | A |
4265684 | Boll | May 1981 | A |
4279790 | Nakajima | Jul 1981 | A |
4340049 | Munsch | Jul 1982 | A |
4485545 | Caverly | Dec 1984 | A |
4501058 | Schutzler | Feb 1985 | A |
4524343 | Morgan et al. | Jun 1985 | A |
4549717 | Dewaegheneire | Oct 1985 | A |
4551974 | Yaeger et al. | Nov 1985 | A |
4553393 | Ruoff | Nov 1985 | A |
4558715 | Walton et al. | Dec 1985 | A |
4567549 | Lemme | Jan 1986 | A |
4585209 | Aine et al. | Apr 1986 | A |
4589179 | Hulting, Jr. | May 1986 | A |
4596483 | Gabriel et al. | Jun 1986 | A |
4619284 | Delarue et al. | Oct 1986 | A |
4654191 | Krieg | Mar 1987 | A |
4684913 | Yaeger | Aug 1987 | A |
4706758 | Johnson | Nov 1987 | A |
4753465 | Dalby | Jun 1988 | A |
4821997 | Zdeblick | Apr 1989 | A |
4823607 | Howe et al. | Apr 1989 | A |
4824073 | Zdeblick | Apr 1989 | A |
4848388 | Waldbusser | Jul 1989 | A |
4854797 | Gourd | Aug 1989 | A |
4864824 | Gabriel et al. | Sep 1989 | A |
4893655 | Anderson | Jan 1990 | A |
4896728 | Wolff et al. | Jan 1990 | A |
4943032 | Zdeblick | Jul 1990 | A |
5060888 | Vezain et al. | Oct 1991 | A |
5061137 | Gourd | Oct 1991 | A |
5061914 | Busch et al. | Oct 1991 | A |
5069419 | Jerman | Dec 1991 | A |
5072288 | MacDonald et al. | Dec 1991 | A |
5102276 | Gourd | Apr 1992 | A |
5114504 | AduJudom, II et al. | May 1992 | A |
5116252 | Hartman | May 1992 | A |
5117916 | Ohta et al. | Jun 1992 | A |
5119555 | Johnson | Jun 1992 | A |
5129753 | Wesley et al. | Jul 1992 | A |
5160233 | McKinnis | Nov 1992 | A |
5190546 | Jervis | Mar 1993 | A |
5192147 | McCloskey | Mar 1993 | A |
5211371 | Coffee | May 1993 | A |
5218998 | Bakken et al. | Jun 1993 | A |
5245738 | Johnson | Sep 1993 | A |
5309717 | Minch | May 1994 | A |
5312152 | Woebkenberg, Jr. et al. | May 1994 | A |
5325880 | Johnson et al. | Jul 1994 | A |
5344117 | Trah et al. | Sep 1994 | A |
5364046 | Dobbs et al. | Nov 1994 | A |
5494113 | Polan | Feb 1996 | A |
5502982 | Venetucci | Apr 1996 | A |
5543349 | Kurtz et al. | Aug 1996 | A |
5605543 | Swanson | Feb 1997 | A |
5619177 | Johnson et al. | Apr 1997 | A |
5622225 | Sundholm | Apr 1997 | A |
5640217 | Hautcoeur et al. | Jun 1997 | A |
5641364 | Golberg et al. | Jun 1997 | A |
5676356 | Ekonen et al. | Oct 1997 | A |
5695504 | Gifford, III et al. | Dec 1997 | A |
5714690 | Burns et al. | Feb 1998 | A |
5722989 | Fitch et al. | Mar 1998 | A |
5771742 | Bokaie et al. | Jun 1998 | A |
5772378 | Keto-Tokoi | Jun 1998 | A |
5796152 | Carr et al. | Aug 1998 | A |
5819749 | Lee et al. | Oct 1998 | A |
5825275 | Wuttig et al. | Oct 1998 | A |
5837394 | Schumm, Jr. | Nov 1998 | A |
5840199 | Warren | Nov 1998 | A |
5850837 | Shiroyama et al. | Dec 1998 | A |
5867302 | Fleming | Feb 1999 | A |
5903099 | Johnson et al. | May 1999 | A |
5916178 | Noone et al. | Jun 1999 | A |
5924492 | Kikuchi et al. | Jul 1999 | A |
5930651 | Terasawa | Jul 1999 | A |
5960812 | Johnson | Oct 1999 | A |
6042553 | Solar et al. | Mar 2000 | A |
6072617 | Henck | Jun 2000 | A |
6073700 | Tsuji et al. | Jun 2000 | A |
6075239 | Aksyuk et al. | Jun 2000 | A |
6080160 | Chen | Jun 2000 | A |
6084849 | Durig et al. | Jul 2000 | A |
6101164 | Kado et al. | Aug 2000 | A |
6110204 | Lazarov et al. | Aug 2000 | A |
6124523 | Banas et al. | Sep 2000 | A |
6126371 | McCloskey | Oct 2000 | A |
6139143 | Brune et al. | Oct 2000 | A |
6195478 | Fouquet | Feb 2001 | B1 |
6203715 | Kim et al. | Mar 2001 | B1 |
6229640 | Zhang | May 2001 | B1 |
6247493 | Henderson | Jun 2001 | B1 |
6277133 | Kanesaka | Aug 2001 | B1 |
6284067 | Schwartz et al. | Sep 2001 | B1 |
6358380 | Mann et al. | Mar 2002 | B1 |
6386507 | Dhuler et al. | May 2002 | B2 |
6406605 | Moles | Jun 2002 | B1 |
6407478 | Wood et al. | Jun 2002 | B1 |
6410360 | Steenberge | Jun 2002 | B1 |
6447478 | Maynard | Sep 2002 | B1 |
6451668 | Neumeier et al. | Sep 2002 | B1 |
6454913 | Rasmussen et al. | Sep 2002 | B1 |
6470108 | Johnson | Oct 2002 | B1 |
6475261 | Matsumoto et al. | Nov 2002 | B1 |
6524322 | Berreklouw | Feb 2003 | B1 |
6533905 | Johnson et al. | Mar 2003 | B2 |
6537310 | Palmaz et al. | Mar 2003 | B1 |
6582985 | Cabuz et al. | Jun 2003 | B2 |
6592724 | Rasmussen et al. | Jul 2003 | B1 |
6596102 | Homma | Jul 2003 | B2 |
6605111 | Bose et al. | Aug 2003 | B2 |
6614570 | Johnson et al. | Sep 2003 | B2 |
6620634 | Johnson et al. | Sep 2003 | B2 |
6624730 | Johnson et al. | Sep 2003 | B2 |
6669794 | Bellouard et al. | Dec 2003 | B1 |
6669795 | Johnson et al. | Dec 2003 | B2 |
6672502 | Paul et al. | Jan 2004 | B1 |
6688828 | Post | Feb 2004 | B1 |
6729599 | Johnson | May 2004 | B2 |
6742761 | Johnson et al. | Jun 2004 | B2 |
6746890 | Gupta et al. | Jun 2004 | B2 |
6771445 | Hamann et al. | Aug 2004 | B1 |
6790298 | Johnson et al. | Sep 2004 | B2 |
6811910 | Tsai et al. | Nov 2004 | B2 |
6840329 | Kikuchi et al. | Jan 2005 | B2 |
6843465 | Scott | Jan 2005 | B1 |
6908275 | Nelson et al. | Jun 2005 | B2 |
6920966 | Buchele et al. | Jul 2005 | B2 |
6955187 | Johnson | Oct 2005 | B1 |
7040323 | Menchaca et al. | May 2006 | B1 |
7044596 | Park | May 2006 | B2 |
7073504 | Callister et al. | Jul 2006 | B2 |
7084726 | Gupta et al. | Aug 2006 | B2 |
7201367 | Wietharn | Apr 2007 | B2 |
7441888 | Johnson | Oct 2008 | B1 |
20010023010 | Yamada et al. | Sep 2001 | A1 |
20020018325 | Nakatani et al. | Feb 2002 | A1 |
20020062154 | Ayers | May 2002 | A1 |
20020106614 | Prince et al. | Aug 2002 | A1 |
20030002994 | Johnson et al. | Jan 2003 | A1 |
20030078465 | Pai et al. | Apr 2003 | A1 |
20030170130 | Johnson | Sep 2003 | A1 |
20040083006 | Ellingsen | Apr 2004 | A1 |
20040200551 | Brhel et al. | Oct 2004 | A1 |
20040221614 | Holemans et al. | Nov 2004 | A1 |
20040243219 | Fischer et al. | Dec 2004 | A1 |
20040249399 | Cinquin et al. | Dec 2004 | A1 |
20050113933 | Carter et al. | May 2005 | A1 |
20060118210 | Johnson | Jun 2006 | A1 |
20060213522 | Menchaca et al. | Sep 2006 | A1 |
20060232374 | Johnson | Oct 2006 | A1 |
20070137740 | Johnson et al. | Jun 2007 | A1 |
20070207321 | Abe et al. | Sep 2007 | A1 |
20070246233 | Johnson | Oct 2007 | A1 |
20090183986 | Johnson et al. | Jul 2009 | A1 |
Number | Date | Country |
---|---|---|
0053596 | Jun 1982 | EP |
0310439 | Apr 1989 | EP |
1122526 | Aug 2001 | EP |
1238600 | Sep 2002 | EP |
2187951 | Sep 1987 | GB |
57161031 | Oct 1982 | JP |
59179771 | Oct 1984 | JP |
07090624 | Apr 1995 | JP |
10173306 | Jun 1998 | JP |
2000185999 | Jul 2000 | JP |
1434314 | Oct 1988 | SU |
WO9853362 | Nov 1998 | WO |
WO9916387 | Apr 1999 | WO |
WO9962432 | Dec 1999 | WO |
WO0004204 | Jan 2000 | WO |
WO03052150 | Jun 2003 | WO |
WO2005108635 | Nov 2005 | WO |
WO2006019943 | Feb 2006 | WO |
Number | Date | Country | |
---|---|---|---|
20090139613 A1 | Jun 2009 | US |