Patent Application
20150023827
This application claims the benefits of the Taiwan Patent Application Serial Number 102126068, filed on Jul. 22, 2013, the subject matter of which is incorporated herein by reference.
1. Field of the Invention
The present invention relates to a porous amorphous alloy artificial joint having suitable Young's modulus, yield strength, porosity and pore size suitable for cell growth, which is manufactured under various pressures and temperatures by virtue of superplasticity of the amorphous alloy in the supercooled liquid (SCL) region.
2. Description of Related Art
Artificial joint can be considered as one of many important progresses in the medical field in the past few centuries, as it benefits many degenerative arthritis patients. The quality of life for those who have lost mobility can be significantly improved after receiving an artificial hip joint or an artificial knee joint. According to statistics, the number of artificial joint replacement in the United States has reached up to 150,000 or more each year, and gradually increases, indicating that it has become a common orthopedic surgery.
The materials used for making an artificial joint must have good corrosion and impact resistances to prevent peripheral cells from over damage during its use. In addition, biocompatible and porous materials are selected as the material for an artificial joint, in order to facilitate cell growth into the artificial joint to promote recovery of lesion. A typical biomedical porous material is generally made by stainless steel or titanium alloy porous material at a processing temperature of up to 1273 K, resulting in overly high Young's modulus and undesirable stress shielding effect, which easily slows down the recovery rate of the affected region that receives the implant.
Therefore, what is needed is to find an artificial joint suitable for cell growth and having an appropriate Young's modulus and yield strength, in order to improve the current state of the art for artificial joints.
An object of the present invention is to provide a porous amorphous alloy artificial joint complying with Young's modulus of the human bones, and having a pore size and porosity suitable for cell growth, to facilitate the application in transplantation of the artificial joints. Another object of the present invention is to provide a method for manufacturing the above porous amorphous alloy artificial joint.
To achieve the above object, the present invention provides a porous amorphous alloy artificial joint formed of at least one of amorphous alloy compounds represented by Formula 1 to Formula 4:
(ZraCubNicAld)100−xSix,
wherein 45≦a≦75, 15≦b≦45, 5≦c≦15, 5≦d≦10, 1≦x≦10, [Formula 1]
ZreCufAggAlh)100 −ySi y
wherein 45≦e≦75, 25≦f≦45, 5≦g≦15, 5≦h≦15, 1≦y≦10, [Formula 2]
TiiTajSikZrl,
wherein 30≦i≦80, 0≦j≦20, 1≦k≦20, 5≦1≦40, [Formula 3]
TimCunZroPdp,
wherein 40≦m≦75, 30≦n≦40, 5≦o≦15, 10≦p≦20. [Formula 4]
The amorphous alloy compound is preferably at least one selected from the group consisting of Zr53Cu30Ni9Al8, (Zr53Cu30Ni9Al8)100−XSiX, Zr48Cu36Ag8Al8, (Zr48Cu36Ag8Al8)100−ySiy, Ti40Zr10Cu36Pd14, Ti60Ta15Si15Zr10, Ti62Ta13Si15Zr10, Ti65Ta10Si15Zr10, Ti60Zr20Ta5Si15, Ti60Zr22Ta3Si15, and Ti45Cu35Zr20, wherein 1≦x≦10, 1≦y≦10, more preferably at least one selected from the group consisting of Zr53Cu30Ni9Al8 and Ti40Zr10Cu36Pd14, and most preferably Zr53Cu30Ni9Al8 and Ti40Zr10Cu36Pd14
The porous amorphous alloy artificial joint has a pore size suitable for cell growth, which is preferably 200-400 and more preferably 250-350 and preferably has a porosity of 40-75%, and more preferably 45-65%. Furthermore, the above-described porous amorphous alloy artificial joint has a Young's modulus and yield strength complying with that of normal joints, wherein the Young's modulus may be 5-25 GPa, and preferably 10-20 GPa, and the yield strength may be 50-350 MPa, and preferably 150-250 MPa.
To prepare the porous amorphous alloy artificial joint, the present invention further provides a method for manufacturing a porous amorphous alloy artificial joint, comprising the following sequential steps:
First, (A) mixing an amorphous alloy power and a water-soluble salt to form a mixture, wherein the porous amorphous alloy power is formed of at least one of amorphous alloy compounds represented by Formula 1 to Formula 4:
(ZraCubNicAld)100−xSix,
wherein 45≦a≦75, 15≦b≦45, 5≦c≦15, 5≦d≦10, 1≦x≦10, [Formula 1]
ZreCufAggAlh)100 −ySi y
wherein 45≦e≦75, 25≦f≦45, 5≦g≦15, 5≦h≦15, 1≦y≦10, [Formula 2]
TiiTajSikZrl,
wherein 30≦i≦80, 0≦j≦20, 1≦k≦20, 5≦1≦40, [Formula 3]
TimCunZroPdp,
wherein 40≦m≦75, 30≦n≦40, 5≦o≦15, 10≦p≦20. [Formula 4]
Afterward, (B) subjecting the mixture to a hot pressing reaction; and then (C) dissolving the water-soluble salt in the mixture to form the porous amorphous alloy artificial joint.
The step (B) can be performed under an inert gas, such as nitrogen, helium, neon, argon, etc. The hot pressing reaction can be performed at a middle temperature of a supercooled liquid region of the porous amorphous alloy power, preferably ½(Tg+Tx)±20K, and more preferably ½(Tg+Tx)±10K. In the case of Zr53Cu30Ni9A18 and Ti40Zr10Cu36Pd14, the minimum temperature of the hot pressing reaction for Zr53Cu30Ni9Al8 is 660K, and the minimum temperature of the hot pressing reaction for Ti40Zr10Cu36Pd14 is 650K.
The hot pressing reaction may be performed under a pressure of 100-500 MPa, and preferably 250-350 MPa. In addition, the reaction time of the hot pressing reaction may be adjusted depending on processing conditions, and is preferably 5-15 minutes, and more preferably 6-12 minutes.
In step (A), the particle size of the amorphous alloy powder may be adjusted as desired, and is preferably 50-300 and more preferably 100-250 In addition, the water-soluble salt can be at least one selected from the group consisting of NaCl, KCl, CaCo3, and CaF2, and preferably NaCl.
The amorphous alloy compound is preferably at least one selected from the group consisting of Zr53Cu30Ni9Al8, (Zr53Cu30Ni9Al8)100−xSix, Zr48Cu36Ag8Al8, (Zr48Cu36Ag8Al8)100−ySiy, Ti40Zr10Cu36Pd14, Ti60Ta15Si15Zr10, Ti62Ta_Si15Zr10, Ti65Ta10Si15Zr10, Ti60Zr20Ta5Si15, Ti60Zr22Ta3Si15, and Ti45Cu35Zr20, wherein 1≦x≦10, 1≦y≦10, more preferably at least one selected from the group consisting of Zr53Cu30Ni9Al8 and Ti40Zr10Cu36Pd14, and most preferably Zr53Cu30Ni9Al8 and Ti40Zr10Cu36Pd14.
In order to manufacture the porous amorphous alloy artificial joint with a preferable pore size, in the step (A), the water-soluble salt is preferably present in an amount of 50-90 vol %, and more preferably 60-70 vol %, based on a total volume of the mixture. Furthermore, a particle size of the water-soluble salt is preferably 150-300 and may be adjusted as desired as well.
The above and other objects, features and other advantages of the present invention will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
Hereinafter, the actions and the effects of the present invention will be explained in more detail via specific examples of the invention. However, these examples are merely illustrative of the present invention and the scope of the invention should not be construed to be defined thereby. In addition, it is evident that various modifications, structures, processes, and changes may be made thereto without departing from the broader spirit and scope of the present disclosure.
In this Example, Zr-based amorphous alloy material was used. A porous artificial joint suitable for cell growth was prepared under various pressures and temperatures by virtue of the superplasticity of the amorphous alloy in the supercooled liquid (SCL) region. NaCl having different particle sizes was added to the Zr-based amorphous powder having a particle size of 50-300 μm, followed by hot pressing.
[Preparation of Porous Amorphous Alloy Powder]
Zr, Cu, Al, and Ni having a purity of 99.99% were molten into Zr53Cu30Ni9Al8 Zr-based alloy ingot by arc-melting (with a power of 350 KW) according to the desired atomic percent of the alloy composition under an argon atmosphere. The alloy ingot was placed in a quartz tube (18 mm in diameter), vacuumed in a quenching melt-spinning chamber to a pressure of 2.0*10−2 mbar and heated by a high-frequency coil (with a power of 5 KW) under vacuum. After melting (about 1-2 minutes), the molten liquid alloy was ejected onto a water-cooled copper wheel by using argon gas with a pressure of 4-6 kg/cm2. The copper wheel was operating at a rotational speed (tangential speed) of 10-20 m/s. For scraping the desired thin strip off from the wheel, a gap was adjusted to less than 1 mm between the copper wheel and the scraper.
The above Zr-based amorphous alloy thin strip was smashed into powder by a blender, and then prepared in the glove box (with an atmosphere of 95% argon, 5% hydrogen). The amorphous alloy powder and tungsten carbide balls were allocated in a weight ratio of 1 (the porous amorphous alloy powder): 10 (tungsten carbide) in a mill jar and ball milled under an atmosphere of pure argon after sealing.
Subsequently, the above substance was placed in a commercial ball mill (SPEX) to perform ball milling, and then the Zr-based amorphous alloy powder with various sizes of (53-297 μm) were sieved out using meshes of different sizes under the protective atmosphere in the glove box.
Tg (glass transition temperature), Tx (crystallization temperature) (10-40 K/min) at various rates were analyzed using non-isothermal DSC (Differential Scanning calorimetry), and then the real Tg, Tx was obtained by linear regression. Afterward, an isothermal DSC analysis was performed at the temperature ranging between the real Tg and Tx. The nucleation curve was obtained from the isothermal DSC analysis as shown in
In addition, as for the Ti40Zr10Cu36Pd1 Ti-based amorphous alloy powder, the hot pressing reaction was performed at a temperature of 650-680 K for less than 480 seconds.
[Preparation of Zr-Based Porous Amorphous Alloy Artificial Joint]
The above Zr53Cu30Ni9Al8 amorphous alloy powder having a density of 6.88 g/cm3 and the NaCl powder having a density of 2.16 g/cm3 were mixed, wherein the particle size of the NaCl powder was between 150-300 μm, and the addition amount of the NaCl powder was calculated according to the following formula:
grams of NaCl=(grams of Zr53Cu30Ni9Al8 powder)/(density of Zr53Cu30Ni9Al8 powder)*(volume percentage of porous amorphous alloy)*(density of NaCl)
Subsequently, with a given particle size of NaCl (150-300 μm), the hot pressing reaction was performed using the amorphous alloy powders of varying sizes (53-297 μm) under varying hot pressing pressures (100-500 MPa). The reaction conditions are summarized in Table 1:
The sectional views of porous amorphous alloy artificial joint in Examples 1 to 8 are shown in
Taking Example 5 and 8 as examples, since interstices may be present between the amorphous alloy powders, or NaCl may encapsulate a few amorphous alloy powders during the process, a particle size of larger than 300 μm may be produced by using NaCl of either 150 μm or 300 μm in diameter.
In summary, in the supercooled liquid region (Tg+Tx)/2, under hot pressing pressure of 100-500 MPa, with an amorphous alloy powder having a particle size of 50-300 μm, the porous artificial joint having a high uniformity, meeting the properties of human joint, and suitable for cell growth can be obtained. Compared to the crystalline metal materials which need to be heated to close the melting point to exhibit a near superplastic property, the amorphous alloy powders Zr53Cu30Ni9Al8 and Ti40Zr10Cu36Pd14 of the present invention can be thermally shaped at 700-740 K, and 650-680 K, respectively, by hot pressing for an average time of 760-1820 seconds, providing advantages in processing ease and convenience.
It should be understood that these examples are merely illustrative of the present invention and the scope of the invention should not be construed to be defined thereby, and the scope of the present invention will be limited only by the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102126068 | Jul 2013 | TW | national |
