US3560274A - Wear-resistant titanium and titanium alloys and method for producing same - Google Patents
Wear-resistant titanium and titanium alloys and method for producing same Download PDFInfo
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- US3560274A US3560274A US866151A US3560274DA US3560274A US 3560274 A US3560274 A US 3560274A US 866151 A US866151 A US 866151A US 3560274D A US3560274D A US 3560274DA US 3560274 A US3560274 A US 3560274A
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title abstract description 34
- 229910052719 titanium Inorganic materials 0.000 title abstract description 34
- 239000010936 titanium Substances 0.000 title abstract description 34
- 229910001069 Ti alloy Inorganic materials 0.000 title abstract description 25
- 238000004519 manufacturing process Methods 0.000 title description 7
- 239000011651 chromium Substances 0.000 abstract description 49
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract description 44
- 229910052804 chromium Inorganic materials 0.000 abstract description 44
- 239000010953 base metal Substances 0.000 abstract description 40
- 239000010410 layer Substances 0.000 abstract description 31
- 238000009792 diffusion process Methods 0.000 abstract description 22
- 238000000137 annealing Methods 0.000 abstract description 14
- 239000002344 surface layer Substances 0.000 abstract description 14
- 238000007747 plating Methods 0.000 abstract description 13
- UMUXBDSQTCDPJZ-UHFFFAOYSA-N chromium titanium Chemical compound [Ti].[Cr] UMUXBDSQTCDPJZ-UHFFFAOYSA-N 0.000 abstract description 9
- 229910000599 Cr alloy Inorganic materials 0.000 abstract description 7
- 239000000788 chromium alloy Substances 0.000 abstract description 7
- 229910045601 alloy Inorganic materials 0.000 description 18
- 239000000956 alloy Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 12
- 229910001040 Beta-titanium Inorganic materials 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 230000032683 aging Effects 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 229910000883 Ti6Al4V Inorganic materials 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000009713 electroplating Methods 0.000 description 4
- 230000004913 activation Effects 0.000 description 3
- 230000001464 adherent effect Effects 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- 238000007669 thermal treatment Methods 0.000 description 3
- 229910052720 vanadium Inorganic materials 0.000 description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052718 tin Inorganic materials 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
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/48—After-treatment of electroplated surfaces
- C25D5/50—After-treatment of electroplated surfaces by heat-treatment
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/941—Solid state alloying, e.g. diffusion, to disappearance of an original layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12458—All metal or with adjacent metals having composition, density, or hardness gradient
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12806—Refractory [Group IVB, VB, or VIB] metal-base component
- Y10T428/12812—Diverse refractory group metal-base components: alternative to or next to each other
Definitions
- An article of titanium or titanium alloy base metal having a hard surface comprising a body of said base rnetal and a diffused zone on the surface of the base metal consisting of essentially of a chromium-stabilized, beta titanium-chromium alloy.
- the present invention is concerned with titanium and titanium alloy articles having hard, wear-resistant surfaces.
- the invention is also concerned with methods for producing such articles.
- titanium and titanium alloys possess properties of strength and light weight which make them highly desirable for a variety of uses.
- such metals have wide application in the space and aircraft industries and more recently are finding utility in components for high speed business machines.
- an object of the present invention is to provide titanium and titanium alloy articles having high surface hardness and improved wear resistance.
- a collateral object is to provide titanium and titanium alloy articles which have the desired properties and which remain substantially unimpaired by solution heat treatment and aging of the base metal.
- a further object of the present invention is to provide a method for producing titanium and titanium alloy articles having high surface hardness and improved resistance to wear, even where the articles are subjected to subsequent solution heat treatment and aging.
- An additional object of the invention is to provide titanium and titanium alloy articles having surface layers or zones which have improved wear resistance and remain highly adherent to the base metal regardless of subsequent impact, wear and thermal treatments.
- the initial chromium layer is sufliciently thin so that upon subsequent diffusion annealing, the chromium is substantially completely diffused into the titanium or titanium alloy workpiece.
- the diffused surface layer is then a chromium rich alloy of titanium-chromium, plus whatever other elements may be alloyed in the substrate.
- the surface layer of titanium-chromium thus formed contains from about 10% to 30% chromium and retains the beta structure on quenching from the beta field, as may occur during subsequent heat treatment.
- the chromium concentration gradually decreases from the surface inwardly of the body. This layer can be subsequently age-hardened, as in an additional aging heat treatment.
- a second layer of chromium-stabilized transformed beta titanium alloy underlies the surface layer and contains from about 10% to 4% of chromium, the chromium content being decreasingly graduated inwardly.
- a third layer of alpha plus unstable beta titanium alloy is formed under the unstable beta layer and contains from 4% to 0% chromium.
- the exact conditions of plating and diffusion annealing may be varied somewhat and this will have an effect on the nature of the layers formed.
- variations in the titanium base metal composition will result in different, but comparable results.
- the titanium base metal is plated with a layer of chromium having a thickness such that it may be substantially completely diffused into the base metal by thermal treatment of practical duration and intensity.
- the chromium plating should have a maximum thickness of about 0.5 mil and preferably 0.3 mil or less.
- the thermal diffusion should be conducted for a period of up to about 24 hours at a maximum temperatures of about l900 F.
- the annealing temperature generally will not be less than about 16-00 F.
- FIG. 1 is a graph, the vertical axis of which is graduated for Knoop hardness, 10 g. load and the horizontal axis for distance from the surface of the base metal in mils.
- the data plotted are derived from tests of a sample prepared in accordance with the invention.
- FIG. 2 is a photomicrograph of a cross-section at the surface of a titanium alloy base metal treated in accordance with the invention.
- the legends adjacent to the photomicrograph identifies the layers formed in the product.
- the tables to the right of the legends set forth estimated chromium content of the layers and hardness data at given distances from the surface of the base metal.
- FIG. 3 includes a similar photomicrograph, legends and tables to those set forth in FIG. 1, but for a base metal sample treated under different conditions.
- the present invention is applicable to titanium metal and titanium based alloys.
- a titanium-base alloy is generally considered to be one containing at least about 50% by weight titanium.
- the invention may be applied to a titanium -6Al-4V alloy.
- the wear resistance of titanium and its alloys is generally unsatisfactory for friction contact applications.
- samples of a Ti6Al-4V alloy were treated.
- Ti-6Al-4V alloy samples of the following composition were employed:
- the sample rods may also be machined into the form of type bars or other printing elements or components of high speed business machines in which surface hardness and wear resistance of the materials are critical.
- Preliminary preparation (1) The titanium alloy rods were chemically polished in a HF--HNO solution to remove disturbed metal from the ground surface. A very slight reduction in the diameter of the samples results from the chemical polishing.
- the rods were activated in the following solution at 120 F. with an anode current density of amp per square foot and a titanium cathode. Initially, an activation period of 40 minutes was employed, but this was found to produce a rough surface. Later, a shorter period of about 2 minutes was adopted and found to be satisfactory for a separate group of samples.
- Chromium plating The titanium alloy rods were electroplated using the chromium plating solution and conditions set forth below:
- Electroplating is the chromium deposition method of choice, but other techniques producing a firmly adherent plate of the desired thickness are acceptable. Thus, vapor plating or other comparable procedure may be followed.
- the articles may be diffusion annealed by placing them in sealed capsules containing a substantially inert atmosphere and heating for the desired period.
- the article may be placed in an Argon-filled Vycor capsule. Annealing temperatures on the order of from about .1600" to 1900 F., are preferred.
- Additional samples A, B, C and D were prepared, generally in accordance with the preceding description. Chromium plate layers of 0.05 and 0.10 mil were applied. The thermal treatments of the samples after diffusion annealing also were varied.
- Samples A and B were diffusion annealed TABLE I.HARDNESS PENETRATION DATA [Ti-6A1-4V Samples, Cr plated, diffusion annealed and solution treated plug aged.]
- Sample A 0.05-mil Cr, 0.10-mil Cr,
- Samples C and D, plated with 0.05 and 0.10 mil of chromium respectively were diffusion annealed and solution heat treated in one treatment for 16 hrs. at 1750 F., water quenched and aged for 6 hrs. at 1000 F., followed by air cooling.
- the hardness data for Sample A are presented graphically in FIG. 1.
- the vertical axis of the graph is graduated, for KHM, g. load, and the horizontal for distance from the surface of the sample, in mils.
- hardness near the surface is on the order of 700 K'HN and decreases gradually to about KHN, about 9 mils from the surface. This shows a high hardness in the surface region influenced by the diffusion annealed chromium, gradually decreasing hardness in the intermediate layers, and substantially lower hardness of the base metal itself.
- the legends below the horizontal axis of the graph identify the metal structures formed in the sample at the depths indicated.
- the articles of the invention will have a Knoop hardness, in at least a portion of the diffused, chromium-stabilized, beta zone, above 500 and usually on the order of from 600 to 700, measured under a 10 g. load.
- the traveFse numbers refer to successive sections taken through the same sample rod in the course of testing hardness, after treatment.
- FIG. 2 is a photomicrograph of a sample prepared by chromium plating to a thickness of about 0.05 mil and diffusion annealing for hrs. at 1700 F. The sample was then air cooled. Activation prior to chromium plating was for 2 minutes.
- the base metal is Ti-6Al-4V.
- the surface layer is a chromium-stabilized stable beta layer having an estimated chromium content ranging from about 30% at the surface to about 11% at a distance of 1.0 mil from the surface.
- the next layer formed by the treatment is a chromiumstabilized transformed beta layer having an estimated chromium content ranging from about 11% at a distance 1.0 mil from the surface to about 4% at a distance between 30 and 4.0 mils from the surface.
- the next layer is a chromium enriched alpha-beta layer having an estimated chromium content ranging from about 4% at a distance of between 3.0 and 4.0 mils from the surface and 0% at a distance approaching 5.0 mils from the surface.
- a scale of the sample dimension in mils keyed to the photomicrograph is provided adjacent to the tabulated hardness and depth data. Note that high hardness was found in the surface layers extending over the zone from about 1.0 mil to 5.0 mils from the surface.
- FIG. 3 is a photomicrograph and related data for another titanium article prepared in accordance with the invention.
- the sample was diffusion annealed for 16 hrs. at 17 00 C., and air cooled. Legends and data identifying the layers, estimated chromium content and hardness of the sample are presented adjacent to the photomicrograph, as in FIG. 2.
- the data indicates high hardness in the surface layers formed by diffusion annealing of the chromium plate and subsequent heat treatment.
- a method for producing an article of titanium or titanium alloy base metal having a hard surface region of high adherence to the base metal comprising:
- said base metal is a titanium alloy comprising by weight about 6% aluminum, 4% vanadium, and the balance substantially all titanium.
- the method of claim 1 which comprises, prior to electroplating, chemically polishing said titanium alloy base meal, degreasing said base metal, repolishing said base metal, and then electrolytically activating said base metal to produce a roughened surface thereon.
- An article of titanium or titanium alloy base metal having a hard surface comprising:
- a diffused zone on the surface of said base metal consisting essentially of an outer surface layer of a chromium-stabilized, beta titanium-chromium alloy containing 30-10% chromium, and
- a second layer of chromium-stabilized transformed beta titanium alloy thereunder containing 10- 4% chromium, and a third layer of alpha plus unstable beta titanium alloy formed thereunder containing from 4% to 0% chromium.
- said diffused zone comprises a portion having a Knoop hardness on the order of from 600 to 700, measured under a 10 g. load.
- titanium base metal is a titanium alloy comprising by weight about 6% aluminum, 4% vanadium and the balance substantially all titanium.
- said outer surface layer extends to a depth of about 1.0 mil in from the surface, wherein said second layer terminates at a distance between 3.0 and 4.0 mils from the surface, and wherein said third layer terminates at a distance approaching 5.0 mils from the surface.
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Abstract
PRODUCING A TITANIUM OR TITANIUM ALLOY BASE METAL ARTICLE HAVING A HARD SURFACE REGION OF HIGH ADHERENCE COMPRISING PLATING THE SURFACE OF THE BASE METAL WITH A LAYER CONSISTING ESSENTIALLY OF CHROMIUM TO A MAXIMUM THICKNESS OF 0.5 MIL AND DIFFUSION ANNEALING THE PLATED ARTICLE TO SUBSTANTIALLY COMPLETELY DIFFUSE THE CHROMIUM INTO THE BASE, THEREBY FORMING A CHROMIUM-STABILIZED SURFACE LAYER OF BETA TITANIUM-CHROMIUM ALLOY ON SAID BASE METAL. AN ARTICLE OF TITANIUM OR TITANIUM ALLOY BASE METAL HAVING A HARD SURFACE COMPRISING A BODY OF SAID BASE METAL AND A DIFFUSED ZONE ON THE SURFACE OF THE BASE METAL CONSISTING OF ESSENTIALLY OF A CHROMIUM-STABILIZED, BETA TITANIUM-CHROMIUM ALLOY.
Description
Feb. 2, 1971 OGDEN 3,560,27Q
WEAR-RESISTANT TITANIUM AND TITANIUM ALLOYS AND METHOD FOR PRODUCING SAME 3 Sheets-Sheet 1 Original Filed July 29. 1966 O H 02 352E.
INVENTOR HORACE R. OGDEN mm m u 5:: $5: gwm iii iii :wm :mm w 252 M23 S10E75 2220110 $219555 592m @9113 mi: Quiz? 205 33.55 M q f w m m O n h h 4 m m O I u M U O O Q m 4 4 D o u m o A U 7 /!OIO m o 0 12: n m
oom -08 U u m 4 H N BY I Qu/wefl any"! ATTOR N EYS United States Patent Oflice Patented Feb. 2, 1971 3,560,274 WEAR-RESISTANT TITANIUM AND TITANIUM ALLOYS AND METHOD FOR PRODUCING SAME Horace R. Ogden, Columbus, Ohio, assignor to International Business Machines Corporation, Armonk, N.Y., a corporation of New York Continuation of application Ser. No. 568,903, July 29, 1966. This application Oct. 10, 1969, Ser. No. 866,151 Int. Cl. C23b 5/06, 5/52; 1332b /00 US. Cl. 14831.5 14 Claims ABSTRACT OF THE DISCLOSURE Producing a titanium or titanium alloy base metal article having a hard surface region of high adherence comprising plating the surface of the base metal with a layer consisting essentially of chromium to a maximum thickness of 0.5 mil and diffusion annealing the plated article to substantially completely diffuse the chromium into the base, thereby forming a chromium-stabilized surface layer of beta titanium-chromium alloy on said base metal.
An article of titanium or titanium alloy base metal having a hard surface comprising a body of said base rnetal and a diffused zone on the surface of the base metal consisting of essentially of a chromium-stabilized, beta titanium-chromium alloy.
This application is a continuation of application Ser. No. 568,903, filed July 29, 1966, now abandoned.
The present invention is concerned with titanium and titanium alloy articles having hard, wear-resistant surfaces. The invention is also concerned with methods for producing such articles.
It is well recognized that titanium and titanium alloys possess properties of strength and light weight which make them highly desirable for a variety of uses. For example, such metals have wide application in the space and aircraft industries and more recently are finding utility in components for high speed business machines.
Despite the basic advantages of titanium and its alloys for many purposes, their resistance to wear is notoriously inadequate for applications involving friction contact. In an attempt to overcome this problem, the metal and its alloys have been provided with various coatings of other metals to alleviate the condition of wear and galling.
.However, prior attempts to coat titanium and titanium alloys have generally been unsatisfactory for a number of reasons. In some cases, the resulting coating or surface layer did not provide hardness on the order sought. In other instances, the coating was not sufiiciently adherent to the base metal, especially where the metal was subsequently subjected to solution heat treating and aging to improve yield strength or other properties.
Accordingly, an object of the present invention is to provide titanium and titanium alloy articles having high surface hardness and improved wear resistance. A collateral object is to provide titanium and titanium alloy articles which have the desired properties and which remain substantially unimpaired by solution heat treatment and aging of the base metal.
A further object of the present invention is to provide a method for producing titanium and titanium alloy articles having high surface hardness and improved resistance to wear, even where the articles are subjected to subsequent solution heat treatment and aging.
An additional object of the invention is to provide titanium and titanium alloy articles having surface layers or zones which have improved wear resistance and remain highly adherent to the base metal regardless of subsequent impact, wear and thermal treatments.
The foregoing objects and many other highly desirable advantages are achieved in accordance with the present invention which comprises, in general, plating a titanium or titanium alloy base metal with a layer of chromium and then substantially completely diffusion annealing the chromium layer into the base metal to develop a hard, chromium-stabilized, beta titanium layer on the surface of the base metal.
Preferably, the initial chromium layer is sufliciently thin so that upon subsequent diffusion annealing, the chromium is substantially completely diffused into the titanium or titanium alloy workpiece. The diffused surface layer is then a chromium rich alloy of titanium-chromium, plus whatever other elements may be alloyed in the substrate. The surface layer of titanium-chromium thus formed contains from about 10% to 30% chromium and retains the beta structure on quenching from the beta field, as may occur during subsequent heat treatment. The chromium concentration gradually decreases from the surface inwardly of the body. This layer can be subsequently age-hardened, as in an additional aging heat treatment. A second layer of chromium-stabilized transformed beta titanium alloy underlies the surface layer and contains from about 10% to 4% of chromium, the chromium content being decreasingly graduated inwardly. A third layer of alpha plus unstable beta titanium alloy is formed under the unstable beta layer and contains from 4% to 0% chromium.
The exact conditions of plating and diffusion annealing may be varied somewhat and this will have an effect on the nature of the layers formed. Likewise, variations in the titanium base metal composition will result in different, but comparable results. In general, the titanium base metal is plated with a layer of chromium having a thickness such that it may be substantially completely diffused into the base metal by thermal treatment of practical duration and intensity. Thus, the chromium plating should have a maximum thickness of about 0.5 mil and preferably 0.3 mil or less. The thermal diffusion should be conducted for a period of up to about 24 hours at a maximum temperatures of about l900 F. The annealing temperature generally will not be less than about 16-00 F.
The invention is described below with reference to the accompanying drawings wherein:
FIG. 1 is a graph, the vertical axis of which is graduated for Knoop hardness, 10 g. load and the horizontal axis for distance from the surface of the base metal in mils. The data plotted are derived from tests of a sample prepared in accordance with the invention.
FIG. 2 is a photomicrograph of a cross-section at the surface of a titanium alloy base metal treated in accordance with the invention. The legends adjacent to the photomicrograph identifies the layers formed in the product. The tables to the right of the legends set forth estimated chromium content of the layers and hardness data at given distances from the surface of the base metal.
FIG. 3 includes a similar photomicrograph, legends and tables to those set forth in FIG. 1, but for a base metal sample treated under different conditions.
The present invention will be more fully appreciated when considered in the light of the following detailed example which is concerned with preferred hard, wearresistant titanium articles and their method of manufacture.
The present invention is applicable to titanium metal and titanium based alloys. A titanium-base alloy is generally considered to be one containing at least about 50% by weight titanium. For example, the invention may be applied to a titanium -6Al-4V alloy.
The titanium and titanium alloys of interest have potential value in the fabrication of components for high speed business machines. For example, Ti-6Al-4V alloys are light-Weight and can be heat treated to high strength levels on the order of 160-170 K.s.i. (K.s.i.=l00 p.s.i.). However, the wear resistance of titanium and its alloys is generally unsatisfactory for friction contact applications. In order to improve surface hardness in accordance with the present invention, samples of a Ti6Al-4V alloy were treated.
The samples were in the form of rods having a diameter of approximately 0.25 inch. Ti-6Al-4V alloy samples of the following composition were employed:
MATERIAL Alloy constituent: Percent by wt. Aluminum 6.3
Vanadium 4.1
Iron 0.14
Carbon 0.027
Oxygen 0.196 Nitrogen 0.016 Hydrogen 0.006 Titanium balance The sample rods may also be machined into the form of type bars or other printing elements or components of high speed business machines in which surface hardness and wear resistance of the materials are critical.
Preliminary preparation (1) The titanium alloy rods were chemically polished in a HF--HNO solution to remove disturbed metal from the ground surface. A very slight reduction in the diameter of the samples results from the chemical polishing.
(2) The rods were then alkaline degreased and rinsed in commercial alkaline cleaner and tap water.
(3) The rods were repolished in the following solution at 85 F. for twenty minutes:
NH FHF-100 g./l. H SiF (31% )-200 ml./l. HNO (70% )400 ml./l. H O (distilled)-Balance After polishing, the samples were rinsed in tap water.
(4) The rods were activated in the following solution at 120 F. with an anode current density of amp per square foot and a titanium cathode. Initially, an activation period of 40 minutes was employed, but this was found to produce a rough surface. Later, a shorter period of about 2 minutes was adopted and found to be satisfactory for a separate group of samples.
Ml./l. Glacial acetic acid 875 Hydrofluoric acid (48%) 125 After activating, the samples were rinsed in tap water.
Chromium plating The titanium alloy rods were electroplated using the chromium plating solution and conditions set forth below:
Chromic acid (CrO )--250 g./l. Sulfuric acid (H SO )--2.5 g./l. Distilled water-Balance Temperaturel30 F.
Current density-300 amp/ sq. ft. Anodes93% Pb7% Sn Plating rate-1 mil per min.
Electroplating is the chromium deposition method of choice, but other techniques producing a firmly adherent plate of the desired thickness are acceptable. Thus, vapor plating or other comparable procedure may be followed.
Diffusion annealing After the chromium plating was completed, the samples were enclosed in argon-filled Vycor capsules and individual rod samples were diffusion annealed according to the following different schedules:
The articles may be diffusion annealed by placing them in sealed capsules containing a substantially inert atmosphere and heating for the desired period. For example, the article may be placed in an Argon-filled Vycor capsule. Annealing temperatures on the order of from about .1600" to 1900 F., are preferred.
Additional samples A, B, C and D were prepared, generally in accordance with the preceding description. Chromium plate layers of 0.05 and 0.10 mil were applied. The thermal treatments of the samples after diffusion annealing also were varied.
Samples A and B, plated with a chromium thickness of 0.05 and 0.10 mil respectively, were diffusion annealed TABLE I.HARDNESS PENETRATION DATA [Ti-6A1-4V Samples, Cr plated, diffusion annealed and solution treated plug aged.]
Distance from surface, mils Sample 0 Sample D Sample A Sample B 0.05-mil Cr, 0.10-mil Cr,
0.05-mil Or, 0.10-mil Cr, Traverse Traverse Traverse Traverse Number Number Number Number Diffusion annealed and solution heat treated 3 Diffusion annealed 16 hrs.
1 Activation treatment prior to Cr plating was {01'40 minutes.
2 1,700 F., air-cooled. Solution heat-treated hour, 1,750 F., waterquenclicd. Aged for 6 hours, at 1,000 F., air-cooled.
In (i113 treatment of 16 hours, at 1,750 F., waterquenelied and aged for 6 hours at 1,000 F., air-coo e for 16 hrs. at 1700 F., air cooled, solution heat treated for /2 hr. at 1750 R, water quenched, and aged for 6 hrs. at 1000 F., followed by air cooling.
Samples C and D, plated with 0.05 and 0.10 mil of chromium respectively were diffusion annealed and solution heat treated in one treatment for 16 hrs. at 1750 F., water quenched and aged for 6 hrs. at 1000 F., followed by air cooling.
Hardness data for three traverses of each sample are set forth in Table I.
The hardness data for Sample A are presented graphically in FIG. 1. The vertical axis of the graph is graduated, for KHM, g. load, and the horizontal for distance from the surface of the sample, in mils.
It will be seen that hardness near the surface is on the order of 700 K'HN and decreases gradually to about KHN, about 9 mils from the surface. This shows a high hardness in the surface region influenced by the diffusion annealed chromium, gradually decreasing hardness in the intermediate layers, and substantially lower hardness of the base metal itself. The legends below the horizontal axis of the graph identify the metal structures formed in the sample at the depths indicated.
Generally, the articles of the invention will have a Knoop hardness, in at least a portion of the diffused, chromium-stabilized, beta zone, above 500 and usually on the order of from 600 to 700, measured under a 10 g. load.
The traveFse numbers refer to successive sections taken through the same sample rod in the course of testing hardness, after treatment.
FIG. 2 is a photomicrograph of a sample prepared by chromium plating to a thickness of about 0.05 mil and diffusion annealing for hrs. at 1700 F. The sample was then air cooled. Activation prior to chromium plating was for 2 minutes. The base metal is Ti-6Al-4V.
As will be seen from the identifying legends accompanying the photomicropgraph, the surface layer is a chromium-stabilized stable beta layer having an estimated chromium content ranging from about 30% at the surface to about 11% at a distance of 1.0 mil from the surface.
The next layer formed by the treatment is a chromiumstabilized transformed beta layer having an estimated chromium content ranging from about 11% at a distance 1.0 mil from the surface to about 4% at a distance between 30 and 4.0 mils from the surface.
The next layer is a chromium enriched alpha-beta layer having an estimated chromium content ranging from about 4% at a distance of between 3.0 and 4.0 mils from the surface and 0% at a distance approaching 5.0 mils from the surface.
A scale of the sample dimension in mils keyed to the photomicrograph is provided adjacent to the tabulated hardness and depth data. Note that high hardness was found in the surface layers extending over the zone from about 1.0 mil to 5.0 mils from the surface.
FIG. 3 is a photomicrograph and related data for another titanium article prepared in accordance with the invention. A Ti6Al-4V alloy rod, activated for 40 minutes as described above, was plated with a 0.05 mil thickness of chromium. The sample was diffusion annealed for 16 hrs. at 17 00 C., and air cooled. Legends and data identifying the layers, estimated chromium content and hardness of the sample are presented adjacent to the photomicrograph, as in FIG. 2.
The data indicates high hardness in the surface layers formed by diffusion annealing of the chromium plate and subsequent heat treatment.
What is claimed is:
1. A method for producing an article of titanium or titanium alloy base metal having a hard surface region of high adherence to the base metal comprising:
(a) electroplating at least a portion of the surface of said base metal with a layer consisting essentially of 6 chromium, said layer having a maximum thickness of 0.5 mil; and
(b) diffusion annealing the resulting plated article in a substantially inert atmosphere at a temperature of 16001900 F. for up to about 24 hours to substantially completely diffuse said chromium into said base metal and to form a high hardness, wear-resistant, chromium-stabilized surface layer of beta titanium-chromium alloy on said base metal.
2. The method of claim 1 wherein said base metal is a titanium alloy comprising by weight about 6% aluminum, 4% vanadium, and the balance substantially all titanium.
3. The method of claim 1 further comprising solution heat treating and aging said article after diffusion annealing to improve the strength thereof.
4. The method of claim 1 wherein said electroplating is conducted to a maximum thickness of 0.3 mil.
5. The method of claim 1 which comprises, prior to electroplating, chemically polishing said titanium alloy base meal, degreasing said base metal, repolishing said base metal, and then electrolytically activating said base metal to produce a roughened surface thereon.
6. An article of titanium or titanium alloy base metal having a hard surface comprising:
(a) a body of said base metal; and
(b) a diffused zone on the surface of said base metal consisting essentially of an outer surface layer of a chromium-stabilized, beta titanium-chromium alloy containing 30-10% chromium, and
a second layer of chromium-stabilized transformed beta titanium alloy thereunder containing 10- 4% chromium, and a third layer of alpha plus unstable beta titanium alloy formed thereunder containing from 4% to 0% chromium.
7. The process of claim 6 wherein said chromium content of each of said zones gradually decreases inwardly.
8. The article of claim 6, wherein the diffused zone has a depth of up to about 10 mils.
9. The article of claim 6, wherein said diffused zone comprises a portion having a Knoop hardness on the order of from 600 to 700, measured under a 10 g. load.
10. The article of claim 6, wherein said titanium base metal is a titanium alloy comprising by weight about 6% aluminum, 4% vanadium and the balance substantially all titanium.
11. The article of claim 6, wherein said outer surface layer extends to a depth of about 1.0 mil in from the surface, wherein said second layer terminates at a distance between 3.0 and 4.0 mils from the surface, and wherein said third layer terminates at a distance approaching 5.0 mils from the surface.
12. The method of claim 1 wherein said high hardness, wear-resistant, chromium-stabilized surface layer of beta titanium-chromium alloy contains 30-10% chromium, and, there is present thereunder in the following order,
a second layer of chromium-stabilized transformed beta titanium alloy containing 104% chromium, and
a third layer of alpha plus unstabled beta titanium alloy formed thereunder wherein the chromium content decreases from 4% to 0%.
13. The process of claim 1 wherein said chromium is electroplated on said base metal in a layer having a maximum thickness of from 0.3 mil to 0.5 mil.
14. The process of claim 1 wherein said diffusion annealing results in a diffused zone having a Knoop hardness on the order of from 600 to 700, measured under a 10 g. period load.
References Cited UNITED STATES PATENTS 2,645,575 7/1953 Herres et al 148l33X (Other references on following page) UNITED 7 STATES PATENTS Abkowitz et al. 148133X Vigor 29--198 Boegehold et a1 29-198X Wagner 29198X Vordahl 148133 Jefferys 29198X Gisser et a1. 29198X Handbook on Titanium, WADC Technical Report, 54-305, Part I, August 1954, pages III-4-8 and III-49.
5 CHARLES N. LOVELL, Primary Examiner U.S. Cl. X.R.
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4236940A (en) * | 1979-06-12 | 1980-12-02 | United Technologies Corporation | Wear resistant titanium alloy coating |
US4588480A (en) * | 1983-06-11 | 1986-05-13 | Mtu Motoren-Und Turbinen-Union Munchen Gmbh | Method of producing wear-protection layers on surfaces of structural parts of titanium or titanium-base alloys |
US4936927A (en) * | 1987-12-17 | 1990-06-26 | Mtu Motoren- Und Turbinen-Union Muenchen Gmbh | Method for applying an aluminum diffusion coating to a component of titanium alloy |
US4946749A (en) * | 1987-05-18 | 1990-08-07 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Coated near-alpha titanium articles |
US5068003A (en) * | 1988-11-10 | 1991-11-26 | Sumitomo Metal Industries, Ltd. | Wear-resistant titanium alloy and articles made thereof |
US5126213A (en) * | 1987-05-18 | 1992-06-30 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Coated near-alpha titanium articles |
WO2005045102A2 (en) * | 2003-11-07 | 2005-05-19 | Aluminal Oberflächentechnik Gmbh & Co. Kg | Coating of substrates |
EP1533401A1 (en) * | 2003-11-14 | 2005-05-25 | Aluminal Oberflächtentechnik GmbH & Co. KG | Electroplating of substrates followed by a diffusion step |
DE19962641B4 (en) * | 1999-12-23 | 2012-04-19 | Erlus Aktiengesellschaft | Method for producing a microstructure on a metallic surface and microstructured metallic surface |
US10015720B2 (en) | 2014-03-14 | 2018-07-03 | GoTenna, Inc. | System and method for digital communication between computing devices |
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1969
- 1969-10-10 US US866151A patent/US3560274A/en not_active Expired - Lifetime
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4236940A (en) * | 1979-06-12 | 1980-12-02 | United Technologies Corporation | Wear resistant titanium alloy coating |
US4588480A (en) * | 1983-06-11 | 1986-05-13 | Mtu Motoren-Und Turbinen-Union Munchen Gmbh | Method of producing wear-protection layers on surfaces of structural parts of titanium or titanium-base alloys |
US4946749A (en) * | 1987-05-18 | 1990-08-07 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Coated near-alpha titanium articles |
US5126213A (en) * | 1987-05-18 | 1992-06-30 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Coated near-alpha titanium articles |
US4936927A (en) * | 1987-12-17 | 1990-06-26 | Mtu Motoren- Und Turbinen-Union Muenchen Gmbh | Method for applying an aluminum diffusion coating to a component of titanium alloy |
US5068003A (en) * | 1988-11-10 | 1991-11-26 | Sumitomo Metal Industries, Ltd. | Wear-resistant titanium alloy and articles made thereof |
DE19962641B4 (en) * | 1999-12-23 | 2012-04-19 | Erlus Aktiengesellschaft | Method for producing a microstructure on a metallic surface and microstructured metallic surface |
WO2005045102A2 (en) * | 2003-11-07 | 2005-05-19 | Aluminal Oberflächentechnik Gmbh & Co. Kg | Coating of substrates |
WO2005045102A3 (en) * | 2003-11-07 | 2006-02-16 | Aluminal Oberflaechentechnik | Coating of substrates |
US20070261965A1 (en) * | 2003-11-07 | 2007-11-15 | Jorg Heller | Coating of Substrates |
EP1533401A1 (en) * | 2003-11-14 | 2005-05-25 | Aluminal Oberflächtentechnik GmbH & Co. KG | Electroplating of substrates followed by a diffusion step |
US10015720B2 (en) | 2014-03-14 | 2018-07-03 | GoTenna, Inc. | System and method for digital communication between computing devices |
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