US20210324533A1 - Anodizing of shape memory materials - Google Patents
Anodizing of shape memory materials Download PDFInfo
- Publication number
- US20210324533A1 US20210324533A1 US17/198,825 US202117198825A US2021324533A1 US 20210324533 A1 US20210324533 A1 US 20210324533A1 US 202117198825 A US202117198825 A US 202117198825A US 2021324533 A1 US2021324533 A1 US 2021324533A1
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- Prior art keywords
- shape memory
- memory material
- material product
- anodizing
- voltage
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- 239000012781 shape memory material Substances 0.000 title claims abstract description 94
- 238000007743 anodising Methods 0.000 title claims abstract description 87
- 239000003792 electrolyte Substances 0.000 claims abstract description 64
- 238000005498 polishing Methods 0.000 claims abstract description 57
- 238000000034 method Methods 0.000 claims description 48
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 21
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000012153 distilled water Substances 0.000 claims description 14
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 11
- 239000010931 gold Substances 0.000 claims description 11
- 229910052737 gold Inorganic materials 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000001117 sulphuric acid Substances 0.000 claims description 6
- 235000011149 sulphuric acid Nutrition 0.000 claims description 6
- 229910001651 emery Inorganic materials 0.000 claims description 5
- 238000005270 abrasive blasting Methods 0.000 claims description 4
- HLXZNVUGXRDIFK-UHFFFAOYSA-N nickel titanium Chemical compound [Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni] HLXZNVUGXRDIFK-UHFFFAOYSA-N 0.000 description 68
- 229910001000 nickel titanium Inorganic materials 0.000 description 67
- 239000007943 implant Substances 0.000 description 36
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 20
- 239000010410 layer Substances 0.000 description 18
- 210000000988 bone and bone Anatomy 0.000 description 15
- 230000000399 orthopedic effect Effects 0.000 description 12
- 229910052759 nickel Inorganic materials 0.000 description 10
- 229940127554 medical product Drugs 0.000 description 6
- 238000003908 quality control method Methods 0.000 description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- 229910052719 titanium Inorganic materials 0.000 description 5
- 206010020751 Hypersensitivity Diseases 0.000 description 4
- 230000007815 allergy Effects 0.000 description 4
- 238000003780 insertion Methods 0.000 description 4
- 230000037431 insertion Effects 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000035876 healing Effects 0.000 description 2
- 229910001092 metal group alloy Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000007521 mechanical polishing technique Methods 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/34—Anodisation of metals or alloys not provided for in groups C25D11/04 - C25D11/32
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/26—Anodisation of refractory metals or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/16—Polishing
- C25F3/22—Polishing of heavy metals
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/16—Polishing
- C25F3/22—Polishing of heavy metals
- C25F3/26—Polishing of heavy metals of refractory metals
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F7/00—Constructional parts, or assemblies thereof, of cells for electrolytic removal of material from objects; Servicing or operating
Definitions
- the present invention relates generally to applying an outer layer to shape memory materials and, more particularly, but not way of limitation, to anodizing shape memory materials such as Nitinol.
- Nitinol which is an alloy containing substantially equal mixtures of nickel and titanium
- Nitinol products such as Nitinol medical implants, therefore are not anodized and thus do not incorporate a protective outer layer.
- Nitinol products are not color anodized such that the Nitinol products may be color coded for product identification, aesthetics, and quality control.
- anodizing of shape memory materials and, in particular, Nitinol will beneficially create Nitinol products that incorporate an outer layer and that may be color coded for product identification, aesthetics, and quality control.
- a shape memory material product or part is anodized as follows.
- the shape memory material product or part is polished, thereby producing a polished shape memory material product or part.
- the polished shape memory material product or part then is anodized.
- the polishing of the shape memory material product or part includes mechanical polishing thereof.
- the mechanical polishing includes but is not limited to paste polishing, polishing with emery paper, or abrasive blasting.
- the polishing of the shape memory material product or part includes electrochemical polishing thereof.
- the electrochemical polishing includes placing the shape memory material product or part in an electrolyte and applying a voltage to the shape memory material product or part for a predetermined time period.
- the voltage for the electrochemical polishing is an anodic voltage between 10V and 60V.
- the predetermined time period for the electrochemical polishing includes but is not limited to between 1 and 60 seconds. Applying the voltage for the electrochemical polishing includes placing a cathode in the electrolyte with the shape memory material product or part therebetween, connecting a negative terminal of a voltage source with the cathode, and connecting a positive terminal of the voltage source with the shape memory material product or part.
- the anodizing of the polished shape memory material product or part includes placing the polished shape memory material product or part in an electrolyte and applying a voltage to the polished shape memory material product or part for a predetermined time period.
- the electrolyte for the anodizing includes phosphoric acid, acetic acid, sulphuric acid, or mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte.
- the electrolyte for the anodizing includes distilled water as a remainder thereof.
- the voltage for the anodizing is an anodic voltage between 10V and 40V.
- the predetermined time period for the anodizing includes but is not limited to between 1 and 120 seconds.
- Applying the voltage for the anodizing includes placing a cathode in the electrolyte adjacent the polished shape memory material product or part, connecting a negative terminal of a voltage source with the cathode, and connecting a positive terminal of the voltage source with the shape memory material product or part.
- a voltage for the anodizing between 29V and 31V and a predetermined time period for the anodizing of 120 seconds produces a gold hue on the polished shape memory material product or part
- a voltage for the anodizing between 24V and 26V and a predetermined time period for the anodizing of 120 seconds produces a blue hue on the polished shape memory material product or part.
- FIG. 1 is a block diagram illustrating electrochemical polishing of a shape memory material industrial or medical product or part.
- FIG. 2 is a block diagram illustrating anodizing of the shape memory material industrial or medical product or part.
- Nitinol due to their superelastic or temperature dependent shape changing properties, include many industrial and medical uses.
- Nitinol which is an alloy containing substantially equal mixtures of nickel and titanium, is utilized in golf club inserts, frames for glasses, cell phone antennae, springs, temperature controls, stents, orthodontic equipment, and the like, and, in particular, orthopedic implants.
- Nitinol orthopedic implants are important in affixing bone, bones, or bone pieces to promote a healing thereof due to their ability to transition between a natural shape and an insertion shape.
- Nitinol orthopedic implants when deformed from their natural shapes to their insertion shapes store energy deliverable to bone, bones, or bone pieces.
- Nitinol orthopedic implants begin in their natural shapes, are transitionable to their insertion shapes, and, once implanted in bone, bones, or bone pieces, attempt to transition from their insertion shapes to their natural shapes whereby the Nitinol orthopedic implants deliver the energy stored therein to the bone, bones, or bone pieces in order to affix the bone, bones, or bone pieces and promote a healing thereof.
- Nitinol industrial and medical products and parts such as Nitinol orthopedic implants cannot be anodized using standard anodizing processes due to their high nickel content although Nitinol industrial and medical products and parts would benefit from anodizing.
- anodized Nitinol industrial and medical products and parts such as Nitinol orthopedic implants would include an outer layer capable of providing protection and, if color anodized, could be color coded for product identification, aesthetics, and quality control.
- an anodized Nitinol orthopedic implant would include an outer layer due to process changes at its surface layer such that the anodized Nitinol orthopedic implant becomes more biocompatible for patients with nickel allergies due to the outer layer that forms a protective barrier between the nickel of the Nitinol orthopedic implant and the patients experiencing nickel allergies.
- Anodizing shape memory materials includes a preparation step involving polishing of the Nitinol employing a chemical/electrochemical polishing technique or a mechanical polishing technique including but not limited to paste polishing, polishing with emery paper, and abrasive blasting with a suitable abrasive media such as sand. Polishing the Nitinol prepares its surface such that the Nitinol is compatible for application of an anodizing technique that generates an oxide on its surface. More particularly, polishing the Nitinol removes from its surface residual oxides that may interfere with the anodizing technique. After polishing, the Nitinol exhibits a generally bright finish on its surface indicating residual oxides have been removed.
- a chemical/electrochemical polishing technique or a mechanical polishing technique including but not limited to paste polishing, polishing with emery paper, and abrasive blasting with a suitable abrasive media such as sand. Polishing the Nitin
- an anodizing step After polishing the Nitinol, an anodizing step generates an oxide on the surface of the Nitinol to form an outer layer that may include a specific color for product identification, aesthetics, and quality control.
- the thickness of the oxide layer may be between 10 nm (nanometers) and 200 nm (nanometers). More particularly, in anodizing the Nitinol, the Nitinol forms an anode for application of an anodizing technique, which may include the Nitinol being fixtured to a titanium rack for electrical contact.
- the cathode for the anodizing technique is any suitable metal such as stainless steel that typically includes a larger surface area than the anode, which, in the preferred embodiment is the Nitinol.
- the electrolyte for the anodizing technique is any suitable electrolyte used in anodizing including but not limited to an electrolyte of phosphoric acid and distilled water with the phosphoric acid in a concentration between 0.5% and 5% total volume of the electrolyte and the remainder of the electrolyte consisting of the distilled water.
- Other electrolytes may include sulfuric acid or acetic acid in distilled water in similar concentration ranges to the phosphoric acid and distilled water.
- the anodizing technique includes applying an anodic voltage between 20 V and 40 V for a predetermined time period including but not limited to between 1 second and 120 seconds, depending on the size of the Nitinol to be anodized and the current limitation of the voltage source.
- the electrolyte may be stirred during application of the anodic voltage although stirring of the electrolyte is not a necessity.
- the temperature of the electrolyte is maintained between 68° F./20° C. and 77° F./25° C. utilizing a water bath, although a higher or lower temperature may produce a successful anodized layer on the Nitinol.
- the Nitinol Upon the expiration of the predetermined time period, the Nitinol will include a homogenous and adherent outer layer of oxide with a thickness between 10-200 nm. Moreover, depending upon the voltage level applied at the anode, the Nitinol will be colored whereby the colors range among blue and gold. As an illustration, a voltage level between 24V and 26V will produce a blue hue on the Nitinol, and a voltage level between 29V and 31V will produce a gold hue on the Nitinol.
- Nitinol implant is mechanically polished until the Nitinol implant exhibits a desired level of polishing using one of the following techniques including but not limited to paste polishing, polishing with emery paper, and abrasive blasting with a suitable abrasive media such as sand.
- the Nitinol implant undergoes fine polishing employing emery paper until a mirror finish is achieved.
- a Nitinol implant 10 may be electrochemically polished.
- An electrolyte 11 is prepared and then placed in a container 12 suitable to hold the electrolyte 11 .
- the electrolyte 11 for the electrochemical polishing technique is any suitable electrolyte used in electrochemical polishing including but not limited to an electrolyte containing methanesulfonic acid in a concentration range of 75%-100% and, if included, sulfuric acid in a concentration range of 2.5%-10%, whereby the density of the electrolyte is 1.5 g/cm 3 at 68° F./20° C. with a pH between 0-1.
- the electrolyte 11 may be a commercially available electrolyte used in electrochemical polishing such as the electrolyte sold by ElpoChem AG, Chriesbaumstr. 4, CH-8064 Volketswil, Switzerland, under the Trade name ElpoLux TI-med.
- a cathode 13 for the electrochemical polishing technique which may be any suitable metal such as stainless steel, is submerged in the electrolyte 11 and connected to a voltage source 14 at its negative terminal 15 .
- the Nitinol implant 10 is submerged in the electrolyte 11 between the cathode 13 and connected to the voltage source 14 at its positive terminal 16 thereby forming an anode 17 for application of the electrochemical polishing technique, which may include the Nitinol implant 10 being fixtured to a titanium rack for electrical contact.
- the cathode 13 typically includes a larger surface area than the anode 17 .
- the electrochemical polishing technique includes utilizing the voltage source 14 to apply an anodic voltage between 10 V and 60 V and, in particular, an anodic voltage of 25 V for a blue color and 30 V for gold color. The anodic voltage is applied for a predetermined time period of between 1 and 60 seconds and, in particular, a time period of 10 seconds.
- the predetermined time period depends on the ability of the voltage source 14 to supply current and the surface area of the Nitinol implant 10 whereby the predetermined time period increases as the size of the Nitinol implant 10 increases.
- the electrolyte 11 may be stirred during application of the anodic voltage although stirring of the electrolyte 11 is not a necessity.
- the temperature of the electrolyte is maintained between 68° F./20° C. and 77° F./25° C. utilizing a water bath, although a higher or lower temperature may produce a successful anodized layer on the Nitinol implant 10 .
- the temperature could also be outside this range and produce a color anodized layer.
- the Nitinol implant 10 Upon the expiration of the predetermined time period, the Nitinol implant 10 is polished and its surface prepared through a removal of residual oxides such that the Nitinol implant 10 is compatible for application of an anodizing technique whereby an oxide may be generated on its surface.
- anodizing of the Nitinol implant 10 as illustrated in FIG. 2 generates an oxide on the surface of the Nitinol implant 10 to form an outer layer that is protective and may include a specific color for product identification, aesthetics, and quality control.
- An electrolyte 20 is prepared and then placed in a container 21 suitable to hold the electrolyte 20 .
- the electrolyte 20 for the anodizing technique is any suitable electrolyte used in anodizing including but not limited to an electrolyte of phosphoric acid, acetic acid, sulphuric acid, or mixtures thereof and distilled water with the phosphoric acid, acetic acid, sulphuric acid, or mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte and the remainder of the electrolyte consisting of the distilled water. More particularly, the electrolyte 20 is an electrolyte with phosphoric acid in a concentration of 0.5% total volume of the electrolyte with the remainder consisting of distilled water.
- a cathode 22 for the anodizing technique which may be any suitable metal such as stainless steel, is submerged in the electrolyte 20 and connected to a voltage source 23 at its negative terminal 24 .
- the Nitinol implant 10 is submerged in the electrolyte 20 adjacent the cathode 22 and connected to the voltage source 23 at its positive terminal 25 thereby forming an anode 26 for application of the anodizing technique, which may include the Nitinol implant 10 being fixtured to a titanium rack for electrical contact.
- the cathode 22 typically includes a larger surface area than the anode 26 .
- the anodizing technique includes utilizing the voltage source 23 to apply an anodic voltage of between 10 V and 40 V and, in particular, an anodic voltage of 25 V to produce a blue color and an anodic voltage of 30 V to produce a gold color.
- the anodic voltage is applied for a predetermined time period of between 1 and 120 seconds to produce the blue or gold color and, in particular, for a time period of 120 seconds.
- the electrolyte 20 may be stirred during application of the anodic voltage although stirring of the electrolyte 20 is not a necessity.
- the temperature of the electrolyte is maintained between 68° F./15° C. and 95° F./35° C. utilizing a water bath.
- the Nitinol implant 10 Upon the expiration of the predetermined time period, the Nitinol implant 10 will include a homogenous and adherent outer layer of oxide with a thickness between 10-200 nm and, in particular, 90 nm for a gold color. Moreover, depending upon the voltage level applied at the anode, the Nitinol will be colored whereby the colors range among gold and blue. As an illustration, a voltage level between 29 V and 31 V will produce a gold hue on the Nitinol, whereas a voltage level between 24V and 26 V will produce a blue hue on the Nitinol. In the foregoing specific example, the anodic voltage of 30 V applied for 120 seconds produces bright gold on the Nitinol implant 10 .
- the Nitinol implant 10 is disconnected from the voltage source 23 and removed from the electrolyte 20 whereby the Nitinol implant 10 includes an outer layer capable of providing protection as well as a color suitable to provide product identification, aesthetics, and quality control. Moreover, the anodized Nitinol implant 10 would include an outer layer due to process changes at its surface layer such that the anodized Nitinol implant 10 becomes more biocompatible for patients with nickel allergies due to the outer layer that forms a protective barrier between the nickel of the Nitinol implant 10 and the patients experiencing nickel allergies.
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Abstract
Anodizing of a shape memory material product or part includes polishing the shape memory material product or part, thereby producing a polished shape memory material product or part, and then anodizing the polished shape memory material product or part. The polishing of the shape memory material product or part includes mechanical polishing or electrochemical polishing. The electrochemical polishing includes placing the shape memory material product or part in an electrolyte and applying a voltage to the shape memory material product or part for a predetermined time. The anodizing of the polished shape memory material product or part includes placing the polished shape memory material product or part in an electrolyte and applying a voltage to the polished shape memory material product or part for a predetermined time period.
Description
- The present invention relates generally to applying an outer layer to shape memory materials and, more particularly, but not way of limitation, to anodizing shape memory materials such as Nitinol.
- Anodizing of metals and metal alloys produces useful benefits including an outer layer that provides protection and an application of color for use in color coding of parts. While many metals and metal alloys may be anodized, certain shape memory materials such as Nitinol, which is an alloy containing substantially equal mixtures of nickel and titanium, cannot be anodized using standard anodizing processes due to its high nickel content. Nitinol products, such as Nitinol medical implants, therefore are not anodized and thus do not incorporate a protective outer layer. Moreover, Nitinol products are not color anodized such that the Nitinol products may be color coded for product identification, aesthetics, and quality control.
- Accordingly, anodizing of shape memory materials and, in particular, Nitinol will beneficially create Nitinol products that incorporate an outer layer and that may be color coded for product identification, aesthetics, and quality control.
- In accordance with the present invention, a shape memory material product or part is anodized as follows. The shape memory material product or part is polished, thereby producing a polished shape memory material product or part. The polished shape memory material product or part then is anodized.
- The polishing of the shape memory material product or part includes mechanical polishing thereof. The mechanical polishing includes but is not limited to paste polishing, polishing with emery paper, or abrasive blasting.
- The polishing of the shape memory material product or part includes electrochemical polishing thereof. The electrochemical polishing includes placing the shape memory material product or part in an electrolyte and applying a voltage to the shape memory material product or part for a predetermined time period. The voltage for the electrochemical polishing is an anodic voltage between 10V and 60V. The predetermined time period for the electrochemical polishing includes but is not limited to between 1 and 60 seconds. Applying the voltage for the electrochemical polishing includes placing a cathode in the electrolyte with the shape memory material product or part therebetween, connecting a negative terminal of a voltage source with the cathode, and connecting a positive terminal of the voltage source with the shape memory material product or part.
- The anodizing of the polished shape memory material product or part includes placing the polished shape memory material product or part in an electrolyte and applying a voltage to the polished shape memory material product or part for a predetermined time period. The electrolyte for the anodizing includes phosphoric acid, acetic acid, sulphuric acid, or mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte. The electrolyte for the anodizing includes distilled water as a remainder thereof. The voltage for the anodizing is an anodic voltage between 10V and 40V. The predetermined time period for the anodizing includes but is not limited to between 1 and 120 seconds. Applying the voltage for the anodizing includes placing a cathode in the electrolyte adjacent the polished shape memory material product or part, connecting a negative terminal of a voltage source with the cathode, and connecting a positive terminal of the voltage source with the shape memory material product or part. As an illustration, a voltage for the anodizing between 29V and 31V and a predetermined time period for the anodizing of 120 seconds produces a gold hue on the polished shape memory material product or part, whereas a voltage for the anodizing between 24V and 26V and a predetermined time period for the anodizing of 120 seconds produces a blue hue on the polished shape memory material product or part.
- It is therefore an object of the present invention to facilitate the anodizing of a shape memory material product or part.
- It is a further object of the present invention to facilitate the anodizing of a shape memory material product or part through a polishing of the shape memory material product or part prior to the anodizing thereof.
- Still other objects, features, and advantages of the present invention will become evident to those of ordinary skill in the art in light of the following. Also, it should be understood that the scope of this invention is intended to be broad, and any combination of any subset of the features, elements, or steps described herein is part of the intended scope of the invention.
-
FIG. 1 is a block diagram illustrating electrochemical polishing of a shape memory material industrial or medical product or part. -
FIG. 2 is a block diagram illustrating anodizing of the shape memory material industrial or medical product or part. - As required, detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention, which may be embodied in various forms. Figures are not necessarily to scale, and some features may be exaggerated to show details of particular components or steps.
- Shape memory materials such as Nitinol, due to their superelastic or temperature dependent shape changing properties, include many industrial and medical uses. Illustratively, Nitinol, which is an alloy containing substantially equal mixtures of nickel and titanium, is utilized in golf club inserts, frames for glasses, cell phone antennae, springs, temperature controls, stents, orthodontic equipment, and the like, and, in particular, orthopedic implants. Nitinol orthopedic implants are important in affixing bone, bones, or bone pieces to promote a healing thereof due to their ability to transition between a natural shape and an insertion shape. Nitinol orthopedic implants when deformed from their natural shapes to their insertion shapes store energy deliverable to bone, bones, or bone pieces. In accordance with their manufacture from shape memory materials, Nitinol orthopedic implants begin in their natural shapes, are transitionable to their insertion shapes, and, once implanted in bone, bones, or bone pieces, attempt to transition from their insertion shapes to their natural shapes whereby the Nitinol orthopedic implants deliver the energy stored therein to the bone, bones, or bone pieces in order to affix the bone, bones, or bone pieces and promote a healing thereof.
- Nitinol industrial and medical products and parts such as Nitinol orthopedic implants cannot be anodized using standard anodizing processes due to their high nickel content although Nitinol industrial and medical products and parts would benefit from anodizing. Illustratively, anodized Nitinol industrial and medical products and parts such as Nitinol orthopedic implants would include an outer layer capable of providing protection and, if color anodized, could be color coded for product identification, aesthetics, and quality control. Moreover, with respect to Nitinol orthopedic implants, an anodized Nitinol orthopedic implant would include an outer layer due to process changes at its surface layer such that the anodized Nitinol orthopedic implant becomes more biocompatible for patients with nickel allergies due to the outer layer that forms a protective barrier between the nickel of the Nitinol orthopedic implant and the patients experiencing nickel allergies.
- Anodizing shape memory materials, and, in particular, the shape memory material Nitinol, includes a preparation step involving polishing of the Nitinol employing a chemical/electrochemical polishing technique or a mechanical polishing technique including but not limited to paste polishing, polishing with emery paper, and abrasive blasting with a suitable abrasive media such as sand. Polishing the Nitinol prepares its surface such that the Nitinol is compatible for application of an anodizing technique that generates an oxide on its surface. More particularly, polishing the Nitinol removes from its surface residual oxides that may interfere with the anodizing technique. After polishing, the Nitinol exhibits a generally bright finish on its surface indicating residual oxides have been removed.
- After polishing the Nitinol, an anodizing step generates an oxide on the surface of the Nitinol to form an outer layer that may include a specific color for product identification, aesthetics, and quality control. In the preferred embodiment, the thickness of the oxide layer may be between 10 nm (nanometers) and 200 nm (nanometers). More particularly, in anodizing the Nitinol, the Nitinol forms an anode for application of an anodizing technique, which may include the Nitinol being fixtured to a titanium rack for electrical contact. The cathode for the anodizing technique is any suitable metal such as stainless steel that typically includes a larger surface area than the anode, which, in the preferred embodiment is the Nitinol. The electrolyte for the anodizing technique is any suitable electrolyte used in anodizing including but not limited to an electrolyte of phosphoric acid and distilled water with the phosphoric acid in a concentration between 0.5% and 5% total volume of the electrolyte and the remainder of the electrolyte consisting of the distilled water. Other electrolytes may include sulfuric acid or acetic acid in distilled water in similar concentration ranges to the phosphoric acid and distilled water. The anodizing technique includes applying an anodic voltage between 20 V and 40 V for a predetermined time period including but not limited to between 1 second and 120 seconds, depending on the size of the Nitinol to be anodized and the current limitation of the voltage source. The electrolyte may be stirred during application of the anodic voltage although stirring of the electrolyte is not a necessity. During the anodizing technique, the temperature of the electrolyte is maintained between 68° F./20° C. and 77° F./25° C. utilizing a water bath, although a higher or lower temperature may produce a successful anodized layer on the Nitinol. Upon the expiration of the predetermined time period, the Nitinol will include a homogenous and adherent outer layer of oxide with a thickness between 10-200 nm. Moreover, depending upon the voltage level applied at the anode, the Nitinol will be colored whereby the colors range among blue and gold. As an illustration, a voltage level between 24V and 26V will produce a blue hue on the Nitinol, and a voltage level between 29V and 31V will produce a gold hue on the Nitinol.
- In order to illustrate the present invention and aid in the understanding thereof, the following example of anodizing a shape memory material industrial or medical product or part and, in particular, a Nitinol orthopedic implant is provided. The Nitinol implant is mechanically polished until the Nitinol implant exhibits a desired level of polishing using one of the following techniques including but not limited to paste polishing, polishing with emery paper, and abrasive blasting with a suitable abrasive media such as sand. Illustratively, the Nitinol implant undergoes fine polishing employing emery paper until a mirror finish is achieved.
- Alternatively, as illustrated in
FIG. 1 , aNitinol implant 10 may be electrochemically polished. Anelectrolyte 11 is prepared and then placed in acontainer 12 suitable to hold theelectrolyte 11. Theelectrolyte 11 for the electrochemical polishing technique is any suitable electrolyte used in electrochemical polishing including but not limited to an electrolyte containing methanesulfonic acid in a concentration range of 75%-100% and, if included, sulfuric acid in a concentration range of 2.5%-10%, whereby the density of the electrolyte is 1.5 g/cm3 at 68° F./20° C. with a pH between 0-1. In a particular example, theelectrolyte 11 may be a commercially available electrolyte used in electrochemical polishing such as the electrolyte sold by ElpoChem AG, Chriesbaumstr. 4, CH-8064 Volketswil, Switzerland, under the Trade name ElpoLux TI-med. Acathode 13 for the electrochemical polishing technique, which may be any suitable metal such as stainless steel, is submerged in theelectrolyte 11 and connected to avoltage source 14 at itsnegative terminal 15. TheNitinol implant 10 is submerged in theelectrolyte 11 between thecathode 13 and connected to thevoltage source 14 at itspositive terminal 16 thereby forming ananode 17 for application of the electrochemical polishing technique, which may include theNitinol implant 10 being fixtured to a titanium rack for electrical contact. In the electrochemical polishing technique, thecathode 13 typically includes a larger surface area than theanode 17. The electrochemical polishing technique includes utilizing thevoltage source 14 to apply an anodic voltage between 10 V and 60 V and, in particular, an anodic voltage of 25 V for a blue color and 30 V for gold color. The anodic voltage is applied for a predetermined time period of between 1 and 60 seconds and, in particular, a time period of 10 seconds. The predetermined time period depends on the ability of thevoltage source 14 to supply current and the surface area of theNitinol implant 10 whereby the predetermined time period increases as the size of theNitinol implant 10 increases. Theelectrolyte 11 may be stirred during application of the anodic voltage although stirring of theelectrolyte 11 is not a necessity. During the electrochemical polishing technique, the temperature of the electrolyte is maintained between 68° F./20° C. and 77° F./25° C. utilizing a water bath, although a higher or lower temperature may produce a successful anodized layer on theNitinol implant 10. The temperature could also be outside this range and produce a color anodized layer. Upon the expiration of the predetermined time period, theNitinol implant 10 is polished and its surface prepared through a removal of residual oxides such that theNitinol implant 10 is compatible for application of an anodizing technique whereby an oxide may be generated on its surface. - After polishing the
Nitinol implant 10, anodizing of theNitinol implant 10 as illustrated inFIG. 2 generates an oxide on the surface of theNitinol implant 10 to form an outer layer that is protective and may include a specific color for product identification, aesthetics, and quality control. Anelectrolyte 20 is prepared and then placed in a container 21 suitable to hold theelectrolyte 20. Theelectrolyte 20 for the anodizing technique is any suitable electrolyte used in anodizing including but not limited to an electrolyte of phosphoric acid, acetic acid, sulphuric acid, or mixtures thereof and distilled water with the phosphoric acid, acetic acid, sulphuric acid, or mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte and the remainder of the electrolyte consisting of the distilled water. More particularly, theelectrolyte 20 is an electrolyte with phosphoric acid in a concentration of 0.5% total volume of the electrolyte with the remainder consisting of distilled water. A cathode 22 for the anodizing technique, which may be any suitable metal such as stainless steel, is submerged in theelectrolyte 20 and connected to avoltage source 23 at itsnegative terminal 24. TheNitinol implant 10 is submerged in theelectrolyte 20 adjacent the cathode 22 and connected to thevoltage source 23 at itspositive terminal 25 thereby forming ananode 26 for application of the anodizing technique, which may include theNitinol implant 10 being fixtured to a titanium rack for electrical contact. In the anodizing technique, the cathode 22 typically includes a larger surface area than theanode 26. The anodizing technique includes utilizing thevoltage source 23 to apply an anodic voltage of between 10 V and 40 V and, in particular, an anodic voltage of 25 V to produce a blue color and an anodic voltage of 30 V to produce a gold color. The anodic voltage is applied for a predetermined time period of between 1 and 120 seconds to produce the blue or gold color and, in particular, for a time period of 120 seconds. Theelectrolyte 20 may be stirred during application of the anodic voltage although stirring of theelectrolyte 20 is not a necessity. During the anodizing technique, the temperature of the electrolyte is maintained between 68° F./15° C. and 95° F./35° C. utilizing a water bath. Upon the expiration of the predetermined time period, theNitinol implant 10 will include a homogenous and adherent outer layer of oxide with a thickness between 10-200 nm and, in particular, 90 nm for a gold color. Moreover, depending upon the voltage level applied at the anode, the Nitinol will be colored whereby the colors range among gold and blue. As an illustration, a voltage level between 29 V and 31 V will produce a gold hue on the Nitinol, whereas a voltage level between 24V and 26 V will produce a blue hue on the Nitinol. In the foregoing specific example, the anodic voltage of 30 V applied for 120 seconds produces bright gold on theNitinol implant 10. TheNitinol implant 10 is disconnected from thevoltage source 23 and removed from theelectrolyte 20 whereby theNitinol implant 10 includes an outer layer capable of providing protection as well as a color suitable to provide product identification, aesthetics, and quality control. Moreover, theanodized Nitinol implant 10 would include an outer layer due to process changes at its surface layer such that theanodized Nitinol implant 10 becomes more biocompatible for patients with nickel allergies due to the outer layer that forms a protective barrier between the nickel of theNitinol implant 10 and the patients experiencing nickel allergies. - Although the present invention has been described in terms of the foregoing preferred embodiment, such description has been for exemplary purposes only and, as will be apparent to those of ordinary skill in the art, many alternatives, equivalents, and variations of varying degrees will fall within the scope of the present invention. That scope, accordingly, is not to be limited in any respect by the foregoing detailed description; rather, it is defined only by the claims that follow.
Claims (22)
1. A method of anodizing a shape memory material product or part, comprising:
polishing the shape memory material product or part, thereby producing a polished shape memory material product or part; and
anodizing the polished shape memory material product or part.
2. The method of anodizing a shape memory material product or part according to claim 1 , wherein polishing the shape memory material product or part comprises mechanical polishing of the shape memory material product or part.
3. The method of anodizing a shape memory material product or part according to claim 2 , wherein the mechanical polishing comprises one of paste polishing, polishing with emery paper, and abrasive blasting.
4. The method of anodizing a shape memory material product or part according to claim 1 , wherein polishing the shape memory material product or part comprises electrochemical polishing of the shape memory material product or part.
5. The method of anodizing a shape memory material product or part according to claim 4 , wherein the electrochemical polishing comprises:
placing the shape memory material product or part in an electrolyte; and
applying a voltage to the shape memory material product or part for a predetermined time period.
6. The method of anodizing a shape memory material product or part according to claim 5 , wherein the voltage for the electrochemical polishing is between 10V and 60V and the predetermined time period for the electrochemical polishing is between 1 and 60 seconds.
7. The method of anodizing a shape memory material product or part according to claim 5 , wherein applying a voltage for the electrochemical polishing comprises:
placing a cathode in the electrolyte with the shape memory material product or part therebetween;
connecting a negative terminal of a voltage source with the cathode; and
connecting a positive terminal of the voltage source with the shape memory material product or part.
8. The method of anodizing a shape memory material product or part according to claim 7 , wherein the voltage for the electrochemical polishing is an anodic voltage between 10V and 60V and the predetermined time period for the electrochemical polishing is between 1 and 60 seconds.
9. The method of anodizing a shape memory material product or part according to claim 1 , wherein anodizing the polished shape memory material product or part comprises:
placing the polished shape memory material product or part in an electrolyte; and
applying a voltage to the polished shape memory material product or part for a predetermined time period.
10. The method of anodizing a shape memory material product or part according to claim 9 , wherein the electrolyte for the anodizing comprises:
one of phosphoric acid, acetic acid, sulphuric acid, and mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte; and
distilled water, whereby a remainder of the electrolyte consists of the distilled water.
11. The method of anodizing a shape memory material product or part according to claim 9 , wherein the voltage for the anodizing is between 10V and 40V and the predetermined time period for the anodizing is between 1 and 120 seconds.
12. The method of anodizing a shape memory material product or part according to claim 9 , wherein a voltage for the anodizing between 29V and 31V and a predetermined time period for the anodizing of 120 seconds produces a gold hue on the polished shape memory material product or part.
13. The method of anodizing a shape memory material product or part according to claim 9 , wherein a voltage for the anodizing between 24V and 26V and a predetermined time period for the anodizing of 120 seconds produces a blue hue on the polished shape memory material product or part.
14. The method of anodizing a shape memory material product or part according to claim 9 , wherein applying a voltage for the anodizing comprises:
placing a cathode in the electrolyte adjacent the polished shape memory material product or part;
connecting a negative terminal of a voltage source with the cathode; and
connecting a positive terminal of the voltage source with the shape memory material product or part.
15. The method of anodizing a shape memory material product or part according to claim 14 , wherein the voltage for the anodizing is an anodic voltage between 10V and 40V and the predetermined time period for the anodizing is between 1 and 120 seconds.
16. A method of anodizing a shape memory material product or part, comprising:
polishing the shape memory material product or part, thereby producing a polished shape memory material product or part, comprising:
placing the shape memory material product or part in an electrolyte, and
applying a voltage to the shape memory material product or part for a predetermined time; and
anodizing the polished shape memory material product or part, comprising:
placing the polished shape memory material product or part in an electrolyte, and
applying a voltage to the polished shape memory material product or part for a predetermined time period.
17. The method of anodizing a shape memory material product or part according to claim 16 , wherein the voltage for the polishing is between 10V and 60V and the predetermined time period for the polishing is between 1 and 60 seconds.
18. The method of anodizing a shape memory material product or part according to claim 16 , wherein the electrolyte for the anodizing comprises:
one of phosphoric acid, acetic acid, sulphuric acid, and mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte; and
distilled water, whereby a remainder of the electrolyte consists of the distilled water.
19. The method of anodizing a shape memory material product or part according to claim 16 , wherein the voltage for the anodizing is between 10V and 40V and the predetermined time period for the anodizing is between 1 and 120 seconds.
20. A method of anodizing a shape memory material product or part, comprising:
mechanically polishing the shape memory material product or part, thereby producing a polished shape memory material product or part; and
anodizing the polished shape memory material product or part, comprising:
placing the polished shape memory material product or part in an electrolyte, and
applying a voltage to the polished shape memory material product or part for a predetermined time period.
21. The method of anodizing a shape memory material product or part according to claim 20 , wherein the electrolyte for the anodizing comprises:
one of phosphoric acid, acetic acid, sulphuric acid, and mixtures thereof in a concentration between 0.1% and 5% total volume of the electrolyte; and
distilled water, whereby a remainder of the electrolyte consists of the distilled water.
22. The method of anodizing a shape memory material product or part according to claim 20 , wherein the voltage for the anodizing is between 10V and 40V and the predetermined time period for the anodizing is between 1 and 120 seconds.
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US17/198,825 US20210324533A1 (en) | 2020-04-17 | 2021-03-11 | Anodizing of shape memory materials |
PCT/IB2021/052897 WO2021209864A1 (en) | 2020-04-17 | 2021-04-07 | Polishing and anodizing of shape memory material parts or products |
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US202063011431P | 2020-04-17 | 2020-04-17 | |
US17/198,825 US20210324533A1 (en) | 2020-04-17 | 2021-03-11 | Anodizing of shape memory materials |
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Citations (2)
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DE10037337A1 (en) * | 2000-03-14 | 2001-09-20 | Nmi Univ Tuebingen | Electropolishing of titanium alloy and nickel-titanium alloy articles, especially Nitinol stents, is carried out in anhydrous electrolyte, preferably sulfamic acid in formamide, with article as anode |
JP2021110006A (en) * | 2020-01-10 | 2021-08-02 | 国立大学法人北見工業大学 | Production method of nickel-titanium alloy having titanium dioxide film |
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US20040117001A1 (en) * | 2001-01-16 | 2004-06-17 | Pelton Alan R. | Medical devices, particularly stents, and methods for their manufacture |
US7488343B2 (en) * | 2003-09-16 | 2009-02-10 | Boston Scientific Scimed, Inc. | Medical devices |
US8216931B2 (en) * | 2005-03-31 | 2012-07-10 | Gang Zhang | Methods for forming multi-layer three-dimensional structures |
AU2008306596B2 (en) * | 2007-10-03 | 2013-04-04 | Accentus Plc | Method of manufacturing metal with biocidal properties |
WO2017130029A1 (en) * | 2016-01-29 | 2017-08-03 | Nanoti Limited | Scratch resistance and corrosion behavior of nanotubular and nano-pitted anodic films on medical grade bulk titanium substrates |
US10106908B1 (en) * | 2017-04-10 | 2018-10-23 | Ryszard Rokicki | Nitinol fatigue resistance using electropolishing, magnetoelectropolishing, anodizing and magnetoanodizing or combinations thereof under oxygen evolution regime |
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2021
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DE10037337A1 (en) * | 2000-03-14 | 2001-09-20 | Nmi Univ Tuebingen | Electropolishing of titanium alloy and nickel-titanium alloy articles, especially Nitinol stents, is carried out in anhydrous electrolyte, preferably sulfamic acid in formamide, with article as anode |
JP2021110006A (en) * | 2020-01-10 | 2021-08-02 | 国立大学法人北見工業大学 | Production method of nickel-titanium alloy having titanium dioxide film |
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