U.S. patent application number 15/483201 was filed with the patent office on 2018-10-11 for nitinol fatigue resistance using electropolishing, magnetoelectropolishing, anodizing and magnetoanodizing or combinations thereof under oxygen evolution regime.
The applicant listed for this patent is Ryszard Rokicki. Invention is credited to Ryszard Rokicki.
Application Number | 20180291522 15/483201 |
Document ID | / |
Family ID | 63710742 |
Filed Date | 2018-10-11 |
United States Patent
Application |
20180291522 |
Kind Code |
A1 |
Rokicki; Ryszard |
October 11, 2018 |
Nitinol Fatigue Resistance Using Electropolishing,
Magnetoelectropolishing, Anodizing and Magnetoanodizing or
Combinations Thereof Under Oxygen Evolution Regime
Abstract
The method for improvement of Nitinol fatigue fracture
resistance may be accomplished by electropolishing or
magnetoelectropolishing under oxygen evolution regime, and by
anodizing or magnetoanodizing the intermetallic compound. All four
processes are performed under an oxygen evolution regime and by
these processes the outermost and subsequent underlying oxide
layers are enriched with oxygen which saturates, fills oxygen
vacancies and bridges surface oxide lattice defects making the
passive oxide layer more stoichiometric and homogenous, elastic
and, as a result of the oxygen enrichment, more fatigue fracture
resistant.
Inventors: |
Rokicki; Ryszard; (Emmaus,
PA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Rokicki; Ryszard |
Emmaus |
PA |
US |
|
|
Family ID: |
63710742 |
Appl. No.: |
15/483201 |
Filed: |
April 10, 2017 |
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C25D 11/26 20130101;
C25D 11/34 20130101; C25F 3/16 20130101 |
International
Class: |
C25F 3/16 20060101
C25F003/16; C25D 11/02 20060101 C25D011/02 |
Claims
1. A process for enhanced cyclic fatigue resistance in Nitinol
intermetallic materials using an electrolytic cell having an anodic
workpiece, a cathode, a container for initiating and maintaining
the dissolution of the material containing Nitinol in an
electrolytic solution maintained at a selected temperature for a
predetermined period of time, said process being maintained under
oxygen evolution (O.sub.2.uparw.) with oxygen generated through
said process being adsorbed into the outer surface layers of the
Nitinol material filling any oxide lattice defects through the
depth of the oxide layer and eliminating inclusion sites and other
micro-fractures at or near the surface by dissolving unwanted
minute surface particles and bridging said inclusion sites and
other micro-fractures in the surface layer of the Nitinol material
resulting in improved cyclic fatigue resistance by the elimination
of said inclusion sites and other micro-fractures strengthening the
surface layers of the Nitinol material to produce greater
stoichiometric homogeneity of the Nitinol material.
2. The process according to claim 1 further including an externally
applied magnetic force from one or more magnets extending entirely
around and circumscribing the electrolytic cell and establishing a
uniform magnetic field therein sufficient to surround and encompass
the cathode and the anodic workpiece for magnetoelectropolishing or
magnetoanodizing the Nitinol material work piece under oxygen
evolution regime (O.sub.2.uparw.).
3. The process according to claim 1, said process being selected
from the group consisting of electropolishing, anodizing, and
appropriate combinations thereof.
4. The process according to claim 2, said process being selected
from the group consisting of electropolishing,
magnetoelectropolishing, anodizing, magnetoanodizing, and
appropriate combinations thereof.
5. The process according to claim 4 for electropolishing and
magnetoelectropolishing a ternary nitinol intermetallic material
under oxygen evolution regime (O.sub.2.uparw.).
6. The process according to claim 5 wherein the ternary element is
selected from the group consisting of Au, Cr, Cu, Fe, Hf, Pd, Pt,
Ta, and Zr.
7. The process according to claim 4 for anodizing and
magnetoanodizing a chemically etched and mechanically polished
ternary nitinol intermetallic material under oxygen evolution
regime (O.sub.2.uparw.).
8. The process according to claim 7 wherein the ternary element is
selected from the group consisting of Au, Cr, Cu, Fe, Hf, Pd, Pt,
Ta, and Zr.
Description
BACKGROUND OF THE INVENTION
[0001] The electropolishing process is almost a 100 year old
electrochemical process applied to metals, metals alloys and
intermetallic compounds for the purposes of smoothing the surface
by minimizing macro and micro roughness, to make the work-piece
surface shiny and reflective, to remove the stressed and deformed
cracked layer (Beilby layer), to improve corrosion resistance, and
in the case of metallic (human body) implants make them more bio-
and hemo-compatible. The electropolishing process mainly uses
direct current (DC), the exception to this regimen is the platinum
metal group, which is electropolished by using alternating current
(AC).
[0002] The electropolishing and magnetoelectropolishing processes
can be performed under two different oxygen regimes, namely; below
and under oxygen evolution. The optimum current density for
electropolishing as well magnetoelectropolishing processes have to
be determined experimentally. Voltage-current curves have to be
plotted and the plateau current density established. In most cases
the best results are obtained when the potential is adjusted to a
value just below the oxygen evolution potential. The best example
of this kind of electropolishing is electropolishing of niobium
cavities for a superconducting installation where surface
smoothness is the main importance. However, many exceptions to the
above rule are reported and occasionally the best polishing is
obtained outside the current density plateau. For many metals,
alloys and intermetallic compounds a second range of potentials and
current densities corresponding to good polishing exists at values
beyond the plateau, i.e., under the conditions of oxygen
evolution.
[0003] Anodizing is an electrolytic process that creates a
homogeneous anodic oxide layer on the surface of some metals,
alloys and intermetallic compounds in order to improve corrosion
and wear resistance and to achieve demanded tribological
properties, etc. Magnetoanodizing is the anodizing process
performed in an externally imposed constant magnetic field. In
connection with the present invention, both of these processes are
to be carried out under an oxygen evolution regime.
[0004] Due to its unique mechanical properties of pseudoelasticity,
shape memory and good corrosion resistance Nitinol has found a
permanent place as an advanced functional biomedical material.
Nitinol is a compound consisting essentially of equal parts of
Nickel and Titanium, represented as NiTi. Nitinol is used in the
production of implantable medical devices, e.g., stents, heart
valve frames, IVC filters, septal occluders, as well as medical and
dental instruments, e.g., arthroscopic instruments, blood clot
stent retrievers, guide wires, endodontic rotary files, etc. The
implantable medical devices, as well as the medical instruments, in
many cases undergo very severe bending, twisting, and cyclic
stretching-contracting conditions during implantation and continued
or continuing use.
[0005] Another advantage of Nitinol as an implantable material is
its resistance to corrosion due to the presence of titanium oxide,
which is the predominant compound residing in the passive film that
spontaneously covers Nitinol on exposure to the ambient atmosphere.
In order to improve corrosion resistance of the passive film layer,
as well as removing other contaminants, smoothing the surface, and
improving fatigue resistance, the material is subjected to
electropolishing as a finishing step prior to sterilization.
[0006] Although titanium oxide is the dominant component in the
passive film layer, it is not the only such component. An
undesirable component of the passive film layer on substantially
all electropolished Nitinol devices is Nickel. The amounts of
Nickel vary depending upon electropolishing protocol used in the
final step of the production of Nitinol medical devices. The sole
presently available electrochemical process for substantially
eliminating and removing Nickel in any form from the surface of
Nitinol, resulting in the creation of pure titanium oxide on the
Nitinol surface, is the magnetoelectropolishing process.
[0007] Generally, Nitinol possesses all of the attributes of a very
good metallic biomaterial, but it is not totally without drawbacks.
The primary drawback is the unavoidable intermetallic inclusions in
Nitinol. Carbides [TiC], oxides [Ti.sub.4Ni.sub.2O.sub.x,
TiO.sub.2] and intermetallic precipitates [Ni.sub.4Ti.sub.3,
Ni.sub.3Ti] are contained within the inclusions. Inclusions are
randomly distributed throughout the entire Nitinol alloy material
with their concentrations depending upon the melting procedure and
purity of each component of the compound during production forming
of the alloy material. Consequently, some of the inclusions will
reside on the surface of the Nitinol material. Any inclusion
formations in Nitinol are unwelcome, but inclusions appearing on
Nitinol surfaces are particularly troublesome, not only because
they are major crack initiation points along with internal
inclusion sites, but also corrosion initiation sites. All bodily
fluids, including blood, contain chlorides which are very corrosive
to all metallic implantable materials including Nitinol. The
corrosion mechanism associated with Nitinol having surface
inclusions immersed in bodily fluids depends on the type of
inclusion, but is intrinsically connected to an affinity of
chloride ions to Nickel.
[0008] In the case of Titanium Carbide [TiC] or Titanium Oxide
[TiO.sub.2], chloride anions will react with the abundant Nickel
content of Nitinol created by the drainage of Titanium from the
matrix which surrounds the inclusion sites during the process of
formation. The Nickel bearing inclusions become the source of free
Nickel that will undergo dissolution in the chloride containing
bodily fluid. Nickel, which is both an allergen and a carcinogen,
will be released into the surrounding environment and into bodily
tissues surrounding the Nitinol implantable device creating
inflammatory and hypersensitivity reactions. For example, in the
case of vascular stents made from Nitinol, the leached Nickel
anions could lead to restenosis which diminishes stent patency.
Another example of a product made from Nitinol is an implantable
permanent birth control or sterilization device for women that is
inserted into and across the fallopian tubes; one such device named
Essure.RTM. is manufactured by Bayer.RTM.. The insertable device
consists of two metal coils, one of which is made of Nitinol. In
many reported cases the Nitinol coil has fractured and become
embedded in or perforates the uterus, and/or migrates to other
organs. In addition, nickel ions, which are released from the
inclusions or from the nickel enriched matrix adjacent to the
inclusions, trigger havoc in women's bodies prone to nickel
allergies resulting in excessive menstrual bleeding, skin rashes,
hair loss, headaches, including migraine headaches, and many more
auto-immune disorders. Simultaneously, the dissolving Nickel from
around inclusion sites and from the inclusions themselves will
weaken the mechanical integrity of the stent or nitinol coil of the
permanently implanted birth control device which will consequently
lead to ultimate fracture.
[0009] Another drawback in using Nitinol is fatigue fracture. The
fracture of Nitinol is a crack initiation and propagation
phenomenon. This means that the existence of a crack is the point
of no return giving rise to fatigue fracture. Taking under
consideration the small diameters and cross sections of medical
devices and tools, the second phase of crack propagation, however
interesting from the material behavior point, is totally irrelevant
from the practical one. The main source of crack initiation is
surface intermetallic inclusions, which accounts for nearly all
cases of Nitinol fracture. According to research undertaken by the
U.S. Food and Drug Administration, Nitinol fatigue fractures are
initiated from surface inclusions in nearly all cases and
micro-cracks caused by cold working stresses, heat effected zones
created by EMC or laser cutting.
[0010] One method which to some degree is capable of removing these
imperfections from the surfaces of Nitinol is the electropolishing
process, which by dissolution action is able to smooth the surface
and by this smoothing eliminates micro-cracks and some of the
minute surface intermetallic inclusions. Almost all Nitinol
electropolishing processes are proprietary, but it is well-known
that all of the processes are performed below the oxygen evolution
regime and in the best cases they are able to improve fatigue life
of Nitinol within a range of only 1/4 to 1/2 fold. Those
proprietary processes performed below the oxygen evolution regime
employ three main groups of electrolytes: 1) methyl
alcohol--sulfuric acid mixture; 2) perchloric--acetic acid mixture;
3) electrolytes containing citric acid. In order to achieve a
higher fatigue life for surface inclusions-free Nitinol medical
implantable devices and instruments the electropolishing process,
as well as the magnetoelectropolishing process, has to be carried
out under an oxygen evolution regime. By applying these processes
the fatigue resistance can be elevated five-fold.
[0011] During electropolishing and magnetoelectropolishing of
Nitinol under an oxygen evolution regime, in addition to
electrolytic smoothing and reduction of nickel content in the
passive protective layer, the Nitinol surface outermost oxide layer
and consecutive deeper under layers are enriched in oxygen without
any significant thickness changes. These additional oxygen ions are
incorporated into the profile of the passive layer and are
responsible for bridging and saturating the oxide lattice defects
making the passive film more stoichiometric and homogeneous. The
more perfect homogeneous oxide with lower lattice defects
consequently improves fatigue resistance of Nitinol medical
implantable devices and instruments by improved elasticity of
titanium oxide crystals covering the surface, which slows the crack
initiation phenomenon. It should be mentioned that electrolytically
introduced oxygen into the passive layer does not enrich the
metal-oxide interface in metallic nickel and its compound as
thermal oxidation processes do and by this process eliminates
another possible source of crack initiation.
[0012] The passive film formation during electropolishing under an
oxygen evolution regime and anodizing can be explained by the
Cabrera & Mott theory. According to high field mechanism for
oxide film formation and growth theory the main prerequisite is the
absorption of oxygen on a metal surface which creates an oxide
monolayer. The next step is electron tunneling from the metal to
the monolayer of adsorbed oxygen which by adding electrons became
an electron trap on the outer surface of the oxide. As the number
of electron traps increases the potential drop across the film
grows. The drop in potential creates the electric field across the
passive film which lowers the activation energy necessary for
further transport of ions through the passive film.
[0013] The oxide on the Nitinol which is composed predominantly of
titanium dioxide [TiO.sub.2] is classified as an N-type
semiconductor which means that anion transport thought the film is
the dominate way of film growth and is due to oxygen ion movement
toward the bulk of the Nitinol intermetallic compound. The
thickening of the oxide film increases the activation energy
necessary for further transport of oxygen ions and limits further
passive film formation. The only way for further growth of the
passive film at this point is to increase the potential drop across
the film which simultaneously increases the electric field.
[0014] When the electropolishing and anodizing under an oxygen
evolution regime are carried out in a magnetic field, i.e.,
magnetoelectropolishing and magnetoanodizing, the properties of
oxygen and its behavior in the magnetic field are the critical
factors. Oxygen is a paramagnetic element with two unpaired
electrons that are attracted and aligned by a magnetic field. Due
to a magnetic field more oxygen will adsorb on the Nitinol surface
and more oxygen ions will be tunneled toward the Nitinol surface
through vacant and dislocation sites. It should be mentioned that
simultaneously more Nickel ions will be leaving the oxide layer and
entering the electrolyte due to its ferromagnetic properties. The
oxide layer will become composed almost entirely of titanium
dioxide [TiO.sub.2]. The highest oxygen concentration will lead to
a higher extent of saturation and bridge lattice defects making the
passive film more homogeneous and elastic with increased fatigue
resistance.
SUMMARY OF THE INVENTION
[0015] The present invention is a method to increase the elasticity
and fatigue fracture resistance of Nitinol [NiTi] by filling out
oxygen vacancies by increasing the depth of the oxide layer,
bridging surface defects, and significantly decreasing the Nickel
content in the outer passive layer of the material. This may be
accomplished by utilizing an electropolishing process, or a
magnetoelectropolishing process, where both processes are carried
out under an Oxygen evolution regime for increasing Oxygen
adsorption of the material during the process. The change in
Nitinol properties may also be accomplished by utilizing an
anodizing process, or a magnetanodizing process, where both
processes are, likewise, carried out under an Oxygen evolution
regime for increasing Oxygen adsorption of the material during the
process.
[0016] Oxygen adsorption causes an Oxygen saturation, enrichment,
and oxygen vacancy reduction through the depth of passive layer of
the material, as well as the bridging of the surface oxide lattice
defects. The resulting Nitinol material will exhibit a more
homogeneous, stoichiometric, protective layer as well as under
layers having an increased oxygen content such that the material
properties are changed resulting in greater elasticity and fatigue
fracture resistance for superior use of the Nitinol material in
implanted devices, arthroscopic tools, and other devices used for
medical or dental purposes on or in the human body.
[0017] The process for enhanced cyclic fatigue resistance in
Nitinol intermetallic materials may be described as using an
electrolytic cell having an anodic workpiece, a cathode, a
container for initiating and maintaining the dissolution of the
material containing Nitinol in an electrolytic solution maintained
at a selected temperature for a predetermined period of time. The
process is to be maintained under oxygen evolution (O.sub.2.uparw.)
with oxygen generated through the process being adsorbed into the
outer surface layers of the Nitinol material filling any oxide
lattice defects through the depth of the oxide layer and
eliminating inclusion sites and other micro-fractures at or near
the surface by dissolving unwanted minute surface particles and
bridging the inclusion sites and other micro-fractures in the
surface layer of the Nitinol material resulting in improved cyclic
fatigue resistance by the elimination of the inclusion sites and
other micro-fractures resulting in the strengthening of the surface
layers of the Nitinol material and producing greater stoichiometric
homogeneity of the Nitinol material.
[0018] The foregoing process can also be utilized with an
externally applied magnetic force from one or more magnets that
extend entirely around and circumscribe the electrolytic cell
establishing a uniform magnetic field within sufficient to surround
and encompass the cathode and the anodic workpiece for
magnetoelectropolishing or magnetoanodizing the Nitinol material
work piece under oxygen evolution regime (O.sub.2.uparw.). The
process can be selected from the group consisting of processes for
electropolishing, anodizing, and appropriate combinations thereof.
The process can also be selected from the group consisting of
electropolishing, magnetoelectropolishing, anodizing,
magnetoanodizing, and appropriate corn binations thereof.
[0019] The process of electropolishing and magnetoelectropolishing
under oxygen evolution regime (O.sub.2.uparw.) can also be utilized
for a ternary nitinol intermetallic material or for anodizing and
magnetoanodizing a chemically etched and mechanically polished
ternary nitinol intermetallic material also under oxygen evolution
regime (O.sub.2.uparw.). If a ternary element is combined with the
Nitinol material the ternary element can be selected from the group
consisting of Au, Cr, Cu, Fe, Hf, Pd, Pt, Ta, and Zr.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0020] The following detailed description is of the best presently
contemplated mode of carrying out the invention. The description is
not intended in a limiting sense, and is made solely for the
purpose of illustrating the general principles of the invention.
The various features and advantages of the present invention may be
more readily understood with reference to the following detailed
description.
[0021] Electropolishing, also known as electrochemical polishing or
electrolytic polishing (especially in the metallography field), is
an electrochemical process that removes material from a metallic
workpiece. It is used to polish, passivate, and deburr metal parts.
It is often described as the reverse of electroplating. It may be
used in lieu of abrasive fine polishing in microstructural
preparation. In an electropolishing process, typically, the
workpiece is immersed in a temperature-controlled bath of
electrolyte and serves as the anode; it is connected to the
positive terminal of a DC power supply, the negative terminal being
attached to the cathode. A current passes from the anode, where
metal on the surface is oxidized and dissolved in the electrolyte,
and transported to the cathode. At the cathode, a reduction
reaction occurs, which normally produces hydrogen.
[0022] Electrolytes used for electropolishing are most often
concentrated acid solutions having a high viscosity, such as
mixtures of sulfuric acid and phosphoric acid. Other
electropolishing electrolytes reported in the literature include
mixtures of perchlorates with acetic anhydride and methanolic
solutions of sulfuric acid. To achieve electropolishing of a rough
surface, the protruding highpoints of a surface profile must
dissolve faster than the recesses. This process, referred to as
anodic leveling, is achieved by a mass transport limited
dissolution reaction. Anodic dissolution under electropolishing
conditions that will deburr metal objects due to increased current
density on corners and burrs.
[0023] Electropolishing of Nitinol is performed in an electrolytic
cell holding a known quantity of electrolyte. The Nitinol material
is attached in the cell as the anode and is suspended in the cell a
predetermined distance beneath the surface of the electrolyte. The
cathode for the process consists of a 316L stainless steel screen
which is positioned around the internal wall of the cell. The
process is performed under a constant potential of 10 volts at an
ambient temperature of approximately 25.degree. C. for a
predetermined period of time under an Oxygen evolution regime.
Oxygen evolution is the process of generating molecular oxygen by
or through a chemical reaction. Mechanisms of oxygen evolution
include the oxidation of water during oxygenic photosynthesis,
electrolysis of water into oxygen and hydrogen, and
electrocatalytic oxygen evolution from oxides and oxoacids. Oxygen
generated by the process is adsorbed into the outer surface layers
of the Nitinol as described herein. Following conclusion of the
immersion electropolishing process, the Nitinol is ultrasonically
cleaned in distilled water.
[0024] Magnetoelectropolishing is performed exactly as in an
electropolishing process with the addition of an externally applied
constant magnetic field of approximately 100 mT. The external
magnetic field is imposed on the electropolishing system by placing
the electrolytic cell within a series of stacked ring magnets that
interact together. The application of the constant magnetic field
has the effect of substantially depleting all ferromagnetic Nickel
from the surface passive layer of Nitinol resulting in the layer
being almost totally consisting of Titanium Dioxide [TiO.sub.2]
upon the termination of the magnetoelectropolishing process.
[0025] Like electropolishing, anodizing is an electrolytic
passivation process used to increase the thickness of the natural
oxide layer on the surface of metal materials to form a protective
coating for the material. The process is called anodizing because
the metal to be treated forms the anode electrode of an electrical
circuit. Anodizing increases corrosion resistance and wear
resistance. Anodization changes the microscopic texture of the
surface and changes the crystal structure of the metal near the
surface of the material. Thick coatings are normally porous, so a
sealing process is often needed to achieve corrosion resistance.
Anodized aluminum surfaces, for example, are harder than aluminum
but have low to moderate wear resistance that can be improved with
increasing thickness or by applying suitable sealing substances.
Anodic films are generally much stronger and more adherent than
most types of paint and metal plating, but also more brittle. This
makes them less likely to crack and peel from aging and wear, but
more susceptible to cracking from thermal stress. An anodized oxide
layer typically has a thickness in the range of 30 nanometers
(1.2.times.10.sup.-6 in.) to several micrometers.
[0026] Typically the anodizing of titanium is used to generate an
array of different colors without dyes, with the anodized titanium
sometimes used in art, costume jewelry, body piercing jewelry and
wedding rings. The resulting color of the anodized metal is
dependent on the thickness of the oxide (which is determined by the
anodizing voltage); and is caused by the interference of light
reflecting off the oxide surface with light traveling through it
and reflecting off the underlying metal surface. Standards for
titanium anodizing are given by AMS 2487 and AMS 2488.
[0027] One example of anodization is presented using aluminum. The
anodized aluminum layer is grown by passing a direct current
through an electrolytic solution, with the aluminum object serving
as the anode (the positive electrode). The current releases
hydrogen at the cathode (the negative electrode) and oxygen at the
surface of the aluminum anode, creating a build-up of aluminum
oxide. Alternating current and pulsed current is also possible but
rarely used. The voltage required by various solutions may range
from 1 to 300 V DC, although most fall in the range of 15 to 21 V
DC. Higher voltages are typically required for thicker coatings
formed in sulfuric and organic acid. The anodizing current varies
with the area of aluminum being anodized, and typically ranges from
30 to 300 amperes/meter.sup.2 (2.8 to 28 amperes/ft.sup.2).
Conditions such as electrolyte concentration, acidity, solution
temperature, and current must be controlled to allow the formation
of a consistent oxide layer. Harder, thicker films tend to be
produced by more dilute solutions at lower temperatures with higher
voltages and currents. The film thickness can range from under 0.5
micrometers for bright decorative work up to 150 micrometers for
architectural applications.
[0028] Like electropolishing, anodizing Nitinol is performed in an
electrolytic cell holding a known quantity of electrolyte. The
Nitinol material is attached in the cell as the anode and is
suspended in the cell a predetermined distance beneath the surface
of the electrolyte. The cathode for the process consists of a
non-reactant metal that will conduct electricity which is
positioned along the internal wall of the cell. During
Magnetoanodizing the magnetic field is imposed on the anodizing
system by placing the electrolytic cell within a series of stacked
ring magnets that interact together. The application of the
constant magnetic field has the effect of substantially depleting
all ferromagnetic Nickel from the surface passive layer of Nitinol
resulting in the layer being almost totally consisting of Titanium
Dioxide [TiO.sub.2] upon the termination of the
magnetoelectropolishing process.
[0029] In all four of the processes described above, free Oxygen
[O.sub.2] is generated and adsorbed by the surface and subsurface
layers of the Nitinol material. The adsorbed oxygen fills any oxide
lattice defects through the depth of the oxide layer and bridges
defects on most of the outer oxide surface layer creating a more
stoichiometric condition and homogeneity in the passive oxide film
layer of the material. This Oxygen enrichment process does not
alter the thickness of the outer protective oxide layer but does
result in the improved fatigue resistance of the material by the
elimination of inclusion sites and other micro-fractures at or near
the surface of the Nitinol material. This phenomenon also greatly
improves the material elasticity which works to retard crack
initiation through continued stretching, shrinking and contorting
of the Nitinol material when used.
EXAMPLES
[0030] A series of groups of Nitinol suture passer needles, used in
mini-invasive arthroscopic surgeries, each underwent three
different electrochemical treatments: [0031] 1.
Magnetoelectropolishing in proprietary electrolyte under oxygen
evolution regime (O.sub.2.uparw.); [0032] 2. Anodizing of
magnetoelectropolished needles under oxygen evolution regime
(O.sub.2.uparw.) in proprietary electrolyte; and, [0033] 3.
Standard electropolishing in methanol-sulfuric acid electrolyte
below oxygen evolution regime.
[0034] Each group of different electrochemically treated needles
consisted of 5 pieces (n=5). The Needles which underwent the
different electrochemical treatments, as listed above, were cyclic
fatigue tested against needles in an "as received condition" that
were manufactured with an EDM--cut, with blue post heat treatment
color. The tested needles were EDM--cut from the same piece of
Nitinol sheet material and had the following dimensions: length--59
mm, width--1.45 mm, and thickness--0.27 mm. The needles were cyclic
fatigue tested using a Mark 10 ESM 301 tester with custom made
fixture with speed of 178 mm/minute. During one complete testing
cycle a needle underwent two continuous bends: first bend
approximating 90.degree., second bend approximating 70.degree.. The
needles were continually tested until fracture occurrence. The
results of the test are tabularized below.
TABLE-US-00001 TABLE 1 Specimen Test 1 Test 2 Test 3 Test 4 Test 5
AVG STDEV AVG-3Sigma Standard, baseline needle 30 31 32 28 29 30
1.4 25.8 (as received with blue post heat treatment color)
Magnetoelectropolished 220 97 179 109 111 143 48.0 -0.8
(O.sub.2.uparw.) Magnetoelectropolished 147 150 161 174 142 155
11.4 120.5 (O.sub.2.uparw.) + Anodize (O.sub.2.uparw.) Standard
electropolishing 37 29 47 36 52 40 8.2 15.5 (below oxygen evolution
regime)
As can be seen from the Table, the highest cyclic fatigue
improvement was achieved by using two consecutive electrochemical
treatments namely magnetoelectropolishing followed by anodizing,
with both processes performed under oxygen evolution regime
(O.sub.2.uparw.). It is also noted that consecutive treatments
(magnetoelectropolishing+anodizing) offers not only an increased
average cycle life until fracture, but also a lower standard
deviation of 11.4 between tested devices.
[0035] The magnetoelectropolished samples have a very similar
average cycle until fracture, however they also possess a larger
standard deviation of 48 between treated samples. As can also be
seen from Table 1, the use of the most commonly applied Nitinol
electropolishing process below oxygen evolution regime gives the
lowest improvement in cyclic fatigue of 40 cycles until fracture,
which translates to 1/4 fold improvement of fatigue resistance
compared with fatigue resistance of "as received" needles.
Moreover, magnetoelectropolished and
magnetoelectropolished+anodized treatments produce a cyclic fatigue
resistance improvement of the Nitinol material devices to
approximately a 5 fold increase compared to "as received" tested
sample needles.
[0036] The foregoing examples and testing provide the insight to
conclude that the combination of the several processes, i.e.,
electropolishing, magnetoelectropolishing, anodizing and
magnetoanodizing, in appropriate process combinations, will result
in a much longer lasting Nitinol material that retains enhanced
fracture fatigue resistance and a much enhanced stoichiometric
homogeneity in its surface layers producing a much better product
for use in the human body that will not leach dissolved metallic
ions through the strengthened surface layers or fracture due to
cyclic bending. Thus, a much safer Nitinol product can be achieved
utilizing the teachings of the appropriate combination of the
foregoing processes.
[0037] The present invention may be embodied in other specific
forms without departing from the spirit or essential attributes
thereof and, accordingly, the described embodiments are to be
considered in all respects as being illustrative and not
restrictive, with the scope of the invention being indicated by the
appended claims, rather than the foregoing detailed description, as
indicating the scope of the invention as well as all modifications
which may fall within a range of equivalency which are also
intended to be embraced therein.
* * * * *