Surface treatment process for implants made of titanium alloy
View Patent ↗A titanium 6 Al/4V alloy is provided with a surface topography that is similar to the Osseotite® surface produced on commercially pure titanium. Native oxide is removed from the Ti 6Al/4V alloy, followed by contacting the metal at ambient temperature with an aqueous hydrochloric acid solution containing a relatively small amount of hydrofluoric acid.
1. A method of producing a uniformly roughened surface on Ti 6/4 alloy for contact with living bone comprising:
(a) removing the native oxide from said Ti 6/4 alloy to expose metal;
(b) contacting said exposed metal with an aqueous solution of 0.005 to 1.0 wt % hydrofluoric acid and 10 to 30 wt % hydrochloric acid for a first period of time to create the desired surface topography having irregularities with peak-to-valley heights of less than 10 microns and average peak-to-peak distance of 1 to 3 microns.
2. The method of claim 1 , wherein the first period of time is about 20 minutes.
3. The method of claim 1 , wherein the aqueous solution includes 0.084 wt % hydrofluoric acid and about 20 wt % hydrochloric acid.
4. The method of claim 1 , wherein the native oxide is removed by contacting the Ti 6/4 alloy with a second aqueous solution of hydrofluoric acid for a second period of time.
5. The method of claim 4 , wherein the second aqueous solution contains about 7.9 to 9.0 wt % hydrofluoric acid.
6. The method of claim 5 , wherein the second aqueous solution contains about 8.45 wt % hydrofluoric acid.
7. A method of producing a uniformly roughened surface on an implant formed of Ti 6/4 alloy for contact with living bone comprising:
treating least a portion of an implant surface with a first aqueous solution including hydrofluoric acid for a first period of time to remove native oxide from the implant surface to create a first surface; and
contacting the first surface with a second aqueous solution including hydrofluoric acid and hydrochloric acid for about twenty (20) minutes at ambient temperature to create a second surface having a topography for osseointegration of the implant with living bone, the topography having peak-to-valley heights of less than 10 microns and average peak-to-peak distance of 1 to 3 microns.
8. The method of claim 7 , wherein the first aqueous solution contains about 7.9 to 9.0 wt % hydrofluoric acid.
9. The method of claim 7 , wherein the second aqueous solution includes about 0.005 to about 1.0 wt % hydrofluoric acid and about 10 to about 30 wt % hydrochloric acid.