US3891456A - Surface treatment of titanium and titanium alloys - Google Patents

Abstract

A process for treating a titanium or titanium alloy surface to improve its bonding characteristics is provided that comprises directing a stream of a slurry of aluminum oxide grit in a hydrofluosilicic acid solution onto the surface for a period of time sufficient to obtain a uniform, oxide-free surface, washing the treated surface to remove grit and terminate acid reaction, and drying the treated surface. The treatment provides a chemically stable surface that is receptive to adhesives and coatings.

Description

United States Patent Hohman et al.

i 1 SURFACE TREATMENT OF TITANIUM AND TITANIUM ALLOYS represented by the Secretary of the Air Force, Washington, DC.

Filed: Oct. 17, 1973 Appl. No.: 407,380

1 June 24, 1975 3275.560 9/1966 Wasserman et a1 .6 252 145 x 3,514.407 5/1970 Missel 252/193 OTHER PUBLICATIONS Metals Handbook, 8th Ed., Vol. 2, 1964. pp. 664-666, [TA472A3].

Primary E.\'aminer-S. Leon Bashore Assistant Examiner-Marc L. Caroff Attorney. Agent, or Firm--Cedric H. Kuhn [57] ABSTRACT A process for treating a titanium or titanium alloy sur- [52] US. Cl. 134/3; 134/7; 134/41;

156/6; 56/18 face to improve its bonding characteristics is provided [51] Int. Cl B08b 3/02 that Comprises directing a stream of a slurry of alumi [58} Field of Search 134/3 7 156/6 num oxide grit in a hydrofluosilicic acid solution onto 252/793 5 the surface for a period of time sufficient to obtain a uniform, oxide-free surface, washing the treated sur- [56] References Cited face to remove grit and terminate acid reaction, and UNITED STATES PATENTS drying the treated surface. The treatment provides a chemically stable surface that is receptive to adhesives 2.413.365 12/1946 McCoy 134/41 x and c0atings 2.605596 8/1952 Uhri 134/7 UX 3010.854 11/1961 Satterfield i. 156/18 6 Claims, 1 Drawing Figure 2/ j 6 5L wees i sup 1, p I 7 PATENTEDJUN24 ms 3, 91,455

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SURFACE TREATMENT OF TITANIUM AND TITANIUM ALLOYS RIGHTS OF THE GOVERNMENT The invention described herein may be manufactured and used by or for the Government of the United States for all governmental purpose without the payment of any royalty.

FIELD OF THE INVENTION The present invention relates to a process for treating the surfaces of articles fabricated from titanium and titanium alloys so as to improve their bonding characteristics.

BACKGROUND OF THE INVENTION It has been over years since the first announcement of production bonding of titanium. The bonded assembly was a firewall sandwhich structure of aluminum honeycomb with titanium and fiberglass skins. The purpose of this design was to take advantage of titaniums heat resistance for a relatively short period of time. However, supersonic aircraft require resistance to elevated temperatures for prolonged periods. The need for bonded assemblies, which will remain structurally sound with high strength-to-weight ratios, has prompted adhesive manufacturers to develop organic adhesives which retain good bond strength at high temperatures. In practice, a great deal of difficulty has been experienced in obtaining consistently durable titanium bonded structures.

While many of the inconsistencies were originally attributed to adhesive problems, a recent study suggests that bonding differences with variously treated titanium alloys were caused by variations in the interfacial structure of the treated adherend. Titanium and its alloys are so reactive that even at room temperature metal oxides are formed. The problem is not just one of providing a clean titanium surface but rather of providing a chemically stable surface receptive to bonding and resistant to degradation. The surface obtained must also promote adhesion without forming a weak surface layer or altering the metallurgical characteristics of the alloy.

A process widely used in industry to treat surfaces of titanium articles involves a multi-step procedure. Briefly, the process includes the steps of l) vapor degreasing, (2) alkaline cleaning, (3) rinsing with water, (4) scale conditioning by contacting with saturated sodium hydroxide at 250F, (5) rinsing with water, (6) removing oxide by contacting with a mixture of nitric and hydrofluoric acids, (7) rinsing with water, (8) conversion coating, (9) rinsing with water, and (I0) drying. An obvious disadvantage of this conventional process is the many steps that are involved in the treatment. A less obvious but greater disadvantage from a quality control standpoint lies in the fact that there is a break in the processing between steps (6) and (8), i.e., between oxide removal and conversion coating by application of a reactive solution. As a result, the freshly cleaned metal rapidly becomes reoxidized before the reactive solution can be applied. When titanium surfaces so treated are bonded to one another, inconsistencies in adhesive reliability are experienced.

[t is an object of this invention, therefore, to provide an improved and simplified process for treating the surfaces of titanium and titanium alloy articles.

Another object of the invention is to provide a process for treating titanium and titanium alloy surfaces in which cleaned surfaces are not subject to reoxidation prior to application of the conversion coating.

A further object of the invention is to provide a process for treating titanium and titanium alloy parts so as to provide chemically stable surfaces which are receptive to bonding and resistant to degradation.

Still another object of the invention is to provide a surface treatment process for titanium alloy adherends that makes it possible to fabricate adhesive-bonded titanium structures having high reliability, high ambient and elevated temperature strengths, and high resistance to corrosive environments and weathering.

Other objects and advantages of the invention will become apparent to those skilled in the art upon consideration of the accompanying disclosure and the drawing in which the sole FIGURE shows a schematic representation of apparatus, partly in perspective, that can be used in carrying out the process of this invention.

SUMMARY OF THE INVENTION The present invention resides in a process for treating parts or articles fabricated from titanium or titanium alloy so as to provide surfaces that are receptive to adhesive bonding. Broadly speaking, the process comprises the step of directing a stream of a slurry of aluminum oxide grit in a hydrofluosilicic acid solution onto a surface of a titanium or titanium alloy part for a period of time sufficient to obtain a uniform, oxide-free surface. Thereafter, the treated surface is washed to remove grit and terminate the acid reaction and then dried.

Prior to contacting the surface with the slurry, the surface is generally cleaned with a solvent to remove oil, grease and other foreign material. This can be conveniently accomplished by wiping the surface with cheese cloth saturated with methyl ethyl ketone or other suitable solvent. in cases where the parts are heavily soiled, they are immersed for a minimum of 5 minutes in an alkaline cleaning solution. The actual time of immersion will depend upon the condition of the parts. Any of the commerically available alkaline cleaners can be utilized in forming the solution. An alkaline cleaner sold under the trade mark Ridoline No. 53 by Amchem Products, Inc., Ambler, Pa., has been found to be effective. The solution is formed by adding the cleaner to a tank of hot water (180F 5F) while agitating the contents to dissolve the solids. After removal from the alkaline cleaning solution, the parts are rinsed with hot water, e.g., by suspending the parts in a hot spray rinse to F) for about 2 minutes.

After completion of the cleaning operation, the bond surface of the titanium or titanium alloy part is vapor blasted with the slurry of aluminum oxide in the aqueous hydrofluosilicic acid solution. The concentration of acid in the solution generally ranges from about 1 to 10 weight percent. However, it has been found that a solution concentration of about 2 percent gives optimum results, being sufficiently strong to etch the titanium yet dilute enough to be easily controlled at minimal material cost. During impingment of the slurry, the treated surface is continuously flooded with the reactive solution under pressure. As a result it is unnecessary to include a wetting agent in the solution.

The amount of aluminum oxide grit contained in the solution generally ranges from about 15 to 25 volume percent, based upon the volume of solution. A ratio of 5 one volume of grit to four volumes of solution has been found to be particularly effective. However, it should be understood that the optimum ratio of grit to solution will depend to a large extent on the equipment used, e.g., its to propel the slurry against the surface. The aluminum oxide used is preferably a purified Al O which is sold commerically as white aluminum oxide abrasive. While it is often preferred to employ 240 grit aluminum oxide, from 180 to 300 grit can be used.

A sand blast gun having a line connected to source of slurry and a line connected to an air supply can be advantageously used in conducting the process. The air pressure is of a magnitude that is sufficient to aspirate the slurry and usually falls in the range of about 70 to 100 psi. However, it is to be understood that the actual air pressure used will depend to a large extent upon the equipment employed and may be higher or lower than the specific pressures indicated. The sand blast gun is provided with a tungsten carbide nozzle having a bore diameter of a size that allows sufficient air to flow to aspirate the slurry into the nozzle.

ln vapor blasting the surface, the nozzle is kept in constant motion to prevent excess metal removal. The angle of impingment of the slurry stream, i.e., the angle between the stream and the treated surface, is less than 90 and is usually from 15 to 45. The period during which the slurry stream is in contact with any one spot on the surface usually falls in the range of about to 60 seconds. To define the contact time in another man ner, the slurry stream is in contact with the bond surface until a uniform, matte surface free from gloss is obtained. In general, the average metal removal rate is about 0.001 inch per treated surface. After completion of the vapor blasting, the part is allowed to remain in contact with the reactive solution for a period that is not in excess of minutes. The contact time generally ranges from about 3 to l5 minutes. At the end of this period, the part is spray rinsed in cold water to remove aluminum oxide grit and stop the acid reaction. Following the water rinse, the part is dried with filtered dry air. The maximum temperature of the air is about l50F.

With some titanium alloys, a smut may be produced on the alloy as a result of the treatment. This smut can be readily removed by submerging the part at room temperature in a nitric acid rinse after the abovementioned water rinse. An immersion of about one minute in 5 percent nitric acid readily removes the smut. Thereafter, the part is spray rinsed in cold water for about 2 minutes. The presence of the smut and the acid treatment for its removal does not have any adverse effect upon the ability of surfaces to be adhesively bonded.

A better understanding of the invention can be obtained by referring to the following illustrative examples which are not intended, however, to be unduly limitative of the invention.

EXAM PLE l A series of runs was conducted in which titanium alloy specimens were surface treated in accordance with the process of this invention. The apparatus employed in the process was substantially the same as that illustrated in the drawing. As shown, container 10 comprises an upper portion H which can be of any appropriate shape, e.g., a cube, a parallelpiped or a cylinder. Attached to the lower end of upper portion II is a lower portion 12 which, as appropriate, is in the form of an inverted pyramid or cone. Resting on the edge where the upper and lower portions intersect is a grate 13. A closure member 14 provided with a vent pipe 16 is adapted to cover the opening in the top of the container.

Attached to the vertex of lower portion l2 and communicating with the interior of the container is one end of a flexible tube 17. The other end of the flexible tube is connected to sand blast gun [8. Tube 19, also connected to the gun and to a source of air, provides means for supplying air to the gun so as to aspirate a slurry 21 of M 0 in hydrofluosilicic acid solution into the nozzle of the gun. The gun has a tungsten carbide nozzle with a bore diameter of one-quarter inch. An opening in the side of container 10 having a rubber seal 22 in the shape of an O-ring positioned therein provides means for inserting the nozzle of gun 18 into the container. Because of the flexibility of the rubber seal, the nozzle can be moved therein so as to direct the slurry at a desired angle onto the titanium or titanium alloy part rest ing on grate 13.

The apparatus is constructed of polymeric materials because of the possibility of corrosive attack by the reactive solution. Thus, container 10 is formed of polyester fiberglass while grate l3 and closure member 14 are fabricated from acrylic. Flexible tube I7 is formed form polyvinyl chloride.

The specimens that were treated were formed from titanium alloys, namely, Ti-6Al-4V and Ti-6Al-6- V-2Sn. In general, the dimensions of the specimens were l X 6 X 0.04 in the case of Ti6Al-4V and l X 6 X 0.045 in the case of Ti-6Al-6V-2Sn.

lnitially, the specimens were solvent cleaned to remove oil, grease and other foreign material. This was accomplished by wiping the surfaces with cheese cloth saturated with methyl ethyl ketone. The specimens were then immersed for a minimum of 5 minutes in an alkaline cleaning solution. (The alkaline cleaning step was not necessary for all specimens, but was used so that the specimens might all be similarly treated.) The alkaline cleaning solution was prepared by filling a thoroughly cleaned tank two-thirds full of tap water and heating to 175F 1' 10F. There was then added 3 to 6 ounces of Ridoline No. 53 per gallon of water at operating level. The tank was next filled to operating level with tap water and heated to lF 5F while agitating the contents to dissolve the solids. The 3-6 oz/gal concentration was maintained by periodic addition of the alkaline cleaner as indicated by chemical analysis. Immediately following immersion in the alkaline bath, the specimens were suspended in a hot spray rinse (l30-l40F) for 2 minutes.

The lower portion of the container shown in the drawing was filled with 2 percent hydrofluosilicic acid solution. There was then added an amount of 240 grit aluminum oxide sufficient to provide a ratio of one volume of grit to 4 volumes of the acid solution.

Surfaces of the specimens disposed on the grate were vapor blasted (about psi air pressure) for a minimum of l5 seconds in any one spot. The nozzle was kept in constant motion to prevent excess metal removal. The total time that the specimens remained in contact with the reactive solution did not exceed inutes. The treated surfaces had a uniform matte surface free from gloss. At the end of this period the speci mens were spray rinsed with cold tap water to remove abrasive and stop the acid reaction. The Ti-6Al-6- V-2Sn specimens were submerged in 5 percent nitric acid for one minute to remove smut after which they were spray rinsed in tap water for 2 minutes. (This step was unnecessary for the Ti-6Al-4V specimens.) After the water rinse, the specimens were dried with filtered dry air with a maximum temperature of 150F.

EXAMPLE ll Utilizing Ti-6Al-4v specimens, treated as described in Example 1, six lap shear specimens were prepared. A primer (EC-2333 primer sold by 3M Co.) was applied, air dried for minutes, and then force dried at [60F for 45 minutes. Using 0.09 lb/ft of epoxy-novolac adhesive (AF-130 adhesive sold by 3M Co.), one-half inch laps were bonded. The cure cycle was 350F for one hour with a heat rise to 350F of 10F per minute. A pressure of 50 psi was maintained throughout the cure. The individual bonded specimens were tested with a grip separation of 0.05 inch/minute.

The results of the shear strength tests conducted at room temperature are shown below in Table 1.

TABLE I Specimen No. Failure Mode Strength. psi

Cohesive Bonded specimens were also prepared that were tested at a temperature of 350F. The specimens were prepared as described above except for a post cure or aging for 2 hours at 350F prior to testing. The results of the shear strength tests are shown below in Table II.

TABLE ll Specimen No. Failure Mode Strength, psi

Cohesive EXAMPLE Ill mens were tested at 600F. The results of the shear strength tests at 600F are shown below in Table lll.

The susceptibility of titanium to reoxidation after surface treatment has always hampered production processes for bonding titanium because of the short period available between cleaning and bonding. A series of runs was conducted to determine an allowable open time" (time between treatment and bonding) for specimens treated according to the procedure described in Example 1. The treated specimens were aged in such a way that air could circulate around the specimens but airborne particulates could not settle on the specimens. Both Ti6Al4V and Ti-6Al-6V-2Sn alloys were included in the runs. After one hour and at daily intervals, six specimens from each alloy were primed with EC-2333 primer, dried, and then bonded with Af-l30 adhesive. The specimens were cured for minutes at 350F. under 50 psi.

The bonded specimens were tested at ambient temperature, and the results of the test are shown below in Table IV.

TABLE [V Lapse Time Shear Stength, psi

Days T 1 -6 A1-4V Ti -6 Al -6V- 2Sn The data in the table show a decline in strength for the Ti-6Al-4V alloy with practically no decline in strength for the Ti-6Al-6V-2Sn alloy. Good bond strengths were obtained with both alloys after an open time" of 9 days.

EXAMPLE V salt spray had equal access to all sides of the exposure section. the procedure and equipment were in accordance with Federal Test Method No. 151A, Method No. 811.1 Salt Spray Test". Specimen sets with the AF130 adhesive were subjected to 30 days of salt spray and tested at 75F and 350F. One specimen set was subjected to 24 hours at 350F, then 7 days of salt spray, and then tested at 350F. Duplicate specimens were fabricated with R34 adhesive and tested as the AF-l bonded specimens except that the elevated temperature was 600F.

To determine the effect of high humidity on bond strength, bonded 0.5 inch lap specimens as described positioned in such a way that condensing humidity had equal access to all sides of the exposure section. Specimen sets with AF-130 adhesive were subjected to 30 days high humidity and tested at F and 350F. One specimen set was subjected to 24 hours at 350F, then 7 days of high humidity, and then tested at 350F. Duplicate specimens were fabricated with FM-34 adhe sive and tested as the AF-130 bonded specimens except that the elevated temperature was 600F.

The result of the above-described runs are set forth below in Tables V and V1. The tables also identify the alloys and adhesives used as well as the cure conditions.

TABLE V Adherends: .040" Titanium 6Al-4V .45" Titanium 6Al-6V-2Sn (machined) Adhesive: AFl30/EC2333 Primer Cure: minutes 350F autoclave Test Temperature: Specified below Type: .5 lap Ave. Shear Test Temp. Strength Adherend Exposure Condition "F (psi) Ti 6-4 Control 75 3158 200 hrs. at 350F 350 2581 24 hrs. at 350F; 7 days R.H., F 350 2153 7 days weatherometer 75 2948 30 days salt spray 7S 3290 30 days salt spray 350 1737 30 days 95% R.H., 100F 75 3071 30 days 95% R.H., 100F 350 1885 24 hrs. at 350F, 7 days salt spray 350 2093 Ti 662 Control 75 3156 30 days salt spray 75 3150 30 days salt spray 350 1806 30 days 95% R.H.. I00F 75 3069 30 days 95% R.H., 100F 350 190i Some evidence of adhesive failure between primer and metal adherend.

Test Temperature:

two hours 550F postcure Specified below Type: .5" lap Ave. Shear Test Temp. Strength Adherend Exposure Condition "F (psi) Ti 6-4 Control 75 3302 hrs. at 600F 600 2138 480 hrs. at 600F 600 2054 1000 hrs. at 600F 600 1848 24 hrs. at 600'F, 7 days 95% R.H. at 100F 600 1888 7 days weatherometer 75 3342 30 days salt spray 75 2065* 30 days salt spray 600 1367 30 days 95% R.H. at l00F 75 2284* 30 days 95% R.H. at 100F 600 1458 24 hrs. at 600F. 7 days salt spray 600 1905 Ti 6-6-2 Control 75 3145 30 days salt spray 75 1883* 30 days salt spray 600 1483 30 days 95% R.H. at 100F 75 1676* 30 days 95% R.H. at l00F 600 1459 Some evidence of adhesive failure between primer and metal adhcrend.

above were subjected to the high humidity condition in paragraph 4.3.5 of Federal Specification MMM-A-l32. Each exposure section was individually The data in the table for the salt spray and high humidity tests show that there is no difference in results due to substrate alloy. The specimens subjected to 30 days of salt spray and then tested at elevated temperatures experienced the greatest loss in shear strength. In the high humidity tests, there was no loss of strength with the AF-l30 adhesive, but the specimen bonded with FM-34 did appear to be degraded with prolonged exposure to moisture.

EXAMPLE VI Runs were conducted to determine the effect of ultraviolet radiation on bond strength. Specimens prepared with both AF-l 30 and FM-340 adhesives, as described in the preceding examples, were cycled for 7 days in an Atlas Weatherometer. This test exposes specimens to 45 minutes of water spray followed by minutes with the spray off. There is continuous ultraviolet radiation from carbon arc lamps. This exposure had no apparent effect on bond strength of either adhesive.

From the foregoing examples, it is seen that the process of this invention provides a simplified, improved procedure for treating the surfaces of titanium alloy parts. The treated surfaces are receptive to adhesive bonding, making possible the fabrication of titanium structures having high ambient and elevated temperature strengths and high resistance to hostile environments. Furthermore, the process eliminates the problem of reoxidation that occurs in conventional processes between cleaning of the surfaces and application of a conversion coating.

As will be evident to those skilled in the art, various modifications of the invention can be made in view of the foregoing disclosure without departing from the spirit or scope of the invention We claim:

1. A process for treating an oxidized surface of a titanium or titanium alloy part which comprises directing a stream consisting essentially of a slurry of aluminum oxide grit in an aqueous hydrofluosilicic acid solution onto the surface for a period of time sufficient to obtain about 3 to [5 minutes; washing the surface with water to remove grit and terminate acid reaction; and drying the part. an oxide-free, uniform, matte surface free from gloss, provided that the total period of time the surface is allowed to remain in contact with the slurry 2. The process according to claim 1 in which the surface is cleaned with a solvent prior to directing the stream thereon.

3. The process according to claim 1 in which the stream is in contact with the surface for about IO to 60 seconds.

4. The process according to claim 3 in which the part is dried with filtered dry air.

5. The process according to claim 1 in which the concentration of acid in the solution ranges from about 1 to l0 weight percent and the amount of aluminum oxide grit in the solution range from about l5 to 25 volume percent, based upon the volume of solution.

6. The process according to claim 1 in which the part is immersed in a nitric acid bath after the water washing step; the part is rinsed with cold tap water after removal from the bath; and the washed part is dried with filtered dry air.

UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION PATENT NO. 1 3, 891,456

DATED June 24, 1975 INVENT R( I Alvin E. Hohman and Gerald W. Lively It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below 301. 3, line 10, after "its", insert capacity Col- 5, line 15, change "v" to V Col. 6, line 37, change "T1" to Ti Col. 9, line 11, change "340" to 34 Col. 10, correct gl i 1 t d as f ll 1, A process for treating an oxidized surface of a titanium or titanium alloy part which comprises directing a stream consisting essentially of a slurry of aluminum oxide grit in an aqueous hydrofluosilicic acid solution onto the surface for a period of time sufficient to obtain an oxide-free, uniform, matte surface free from gloss, provided that the total period of time the surface is allowed to remain in contact with the slurry is about 3 to 15 minutes; washing the surface with water to remove grit and terminate acid reaction; and drying the part.

Signed and Scaled this ninth D3) Of December1975 [SEAL] Attest:

RUTH. C. MASON C. MARSHALL DANN Alresrmg Offrcer Commissioner of Parents and Trademarks

Claims (6)

1. A PROCESS FOR TREATING AN OXIDEZED SURFACE OF A TITANIUM OR TITANIUM ALLOY PART WHICH COMPRISES DIRECTING AN STREAM CONSISTING ESSENTIALLY OF A SLURRY OF ALUMINUM OXIDE GRIT IN AN AQUEOUS HYDROFLUOSILICIC ACID SOLUTION ONTO THE SURFACE FOR A PERIOD OF TIME SUFFICIENT TO OBTAIN ABOUT 3 TO 15 MINUTES; WASHING THE SURFACE WITH WATER TO REMOVE GRIT AND TERMINATE ACID REACTION; AND DRYING THE PART, AN OXIDE-FREE, UNIFORM, MATTE SURFACE FREE FROM GLOSS, PROVIDED THAT THE TOTAL PERIOD OF TIME THE SURFACE IS ALLOWED TO REMAIN IN CONTACT WITH THE SLURRY IS.

2. The process according to claim 1 in which the surface is cleaned with a solvent prior to directing the stream thereon.

3. The process according to claim 1 in which the stream is in contact with the surface for aBout 10 to 60 seconds.

4. The process according to claim 3 in which the part is dried with filtered dry air.

5. The process according to claim 1 in which the concentration of acid in the solution ranges from about 1 to 10 weight percent and the amount of aluminum oxide grit in the solution range from about 15 to 25 volume percent, based upon the volume of solution.

6. The process according to claim 1 in which the part is immersed in a nitric acid bath after the water washing step; the part is rinsed with cold tap water after removal from the bath; and the washed part is dried with filtered dry air.

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