Method of bonding titanium to stainless steel
First Claim
1. A method of making a living tissue implantable component assembly, comprising the steps of:
- selecting a biocompatible 316L stainless steel part;
selecting a biocompatible titanium part that is comprised of Ti-6Al-4V;
selecting a laminated filler material that is less than about 0.010 inches thick that is comprised of a 22% to 98% nickel portion and a remaining titanium portion, said laminated filler material comprising at least two nickel layers surrounding at least one titanium layer,selecting said laminated filler material having a melting point that is lower than the melting point of said titanium part and said stainless steel part;
positioning said filler material between said stainless steel part and said titanium part;
placing the assembly in a non-reactive atmosphere;
applying a force to said stainless steel part and said titanium part to place said filler material in compression, thereby creating intimate contact between said stainless steel part, said filler material, and said titanium part;
heating the assembly to a temperature between said melting point of said laminated filler material and said melting point of said titanium part;
holding the assembly at said bonding temperature for a predetermined time to form a bond between said stainless steel part and said titanium part;
cooling the assembly; and
implanting the component assembly in a human body.
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Accused Products
Abstract
A method of bonding a stainless steel part to a titanium part by heating a component assembly comprised of the titanium part, the stainless steel part, and a laminated titanium-nickel filler material placed between the two parts and heated at a temperature that is less than the melting point of either the stainless steel part or the titanium part. The component assembly is held in intimate contact at temperature in a non-reactive atmosphere for a sufficient time to develop a hermetic and strong bond between the stainless steel part and the titanium part. The bonded component assembly is optionally treated with acid to remove any residual free nickel and nickel salts, to assure a biocompatible component assembly, if implanted in living tissue.
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Citations
11 Claims
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1. A method of making a living tissue implantable component assembly, comprising the steps of:
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selecting a biocompatible 316L stainless steel part; selecting a biocompatible titanium part that is comprised of Ti-6Al-4V; selecting a laminated filler material that is less than about 0.010 inches thick that is comprised of a 22% to 98% nickel portion and a remaining titanium portion, said laminated filler material comprising at least two nickel layers surrounding at least one titanium layer, selecting said laminated filler material having a melting point that is lower than the melting point of said titanium part and said stainless steel part; positioning said filler material between said stainless steel part and said titanium part; placing the assembly in a non-reactive atmosphere; applying a force to said stainless steel part and said titanium part to place said filler material in compression, thereby creating intimate contact between said stainless steel part, said filler material, and said titanium part; heating the assembly to a temperature between said melting point of said laminated filler material and said melting point of said titanium part; holding the assembly at said bonding temperature for a predetermined time to form a bond between said stainless steel part and said titanium part; cooling the assembly; and
implanting the component assembly in a human body. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10)
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11. A method of making a living tissue implantable component assembly, comprising the steps of:
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selecting a biocompatible stainless steel part from the group consisting of corrosion resistant stainless steels; selecting a biocompatible titanium part comprised of Ti-6Al-4V; positioning a laminated filler material between said stainless steel part and said titanium part; applying a force to said stainless steel part and said titanium part to place said filler material in compression between 5 and 7 psi, thereby forming said component assembly; placing said component assembly in a non-reactive atmosphere; heating said component assembly to between approximately 940° and
1260°
C. for between approximately 5 and 60 minutes;cooling said component assembly; cleaning said component assembly after cooling to remove elemental nickel and nickel salts; and implanting the component assembly into a human body.
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Specification