US2924517A - Copper base prealloy for addition to zinc - Google Patents
Copper base prealloy for addition to zinc Download PDFInfo
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- US2924517A US2924517A US724890A US72489058A US2924517A US 2924517 A US2924517 A US 2924517A US 724890 A US724890 A US 724890A US 72489058 A US72489058 A US 72489058A US 2924517 A US2924517 A US 2924517A
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- alloy
- aluminum
- iron
- zirconium
- zinc
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- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title claims description 68
- 229910052725 zinc Inorganic materials 0.000 title claims description 68
- 239000011701 zinc Substances 0.000 title claims description 68
- 229910052802 copper Inorganic materials 0.000 title claims description 34
- 239000010949 copper Substances 0.000 title claims description 34
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims description 33
- 229910045601 alloy Inorganic materials 0.000 claims description 112
- 239000000956 alloy Substances 0.000 claims description 112
- 239000002245 particle Substances 0.000 claims description 48
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 40
- 229910052782 aluminium Inorganic materials 0.000 claims description 37
- -1 IRON-ZIRCONIUM-ALUMINUM Chemical compound 0.000 claims description 33
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 33
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 22
- 229910052726 zirconium Inorganic materials 0.000 claims description 21
- 229910052742 iron Inorganic materials 0.000 claims description 19
- 239000011159 matrix material Substances 0.000 claims description 9
- 229910000838 Al alloy Inorganic materials 0.000 description 13
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 10
- 229910052749 magnesium Inorganic materials 0.000 description 10
- 239000011777 magnesium Substances 0.000 description 10
- 230000008018 melting Effects 0.000 description 10
- 238000002844 melting Methods 0.000 description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 238000005275 alloying Methods 0.000 description 5
- 238000005266 casting Methods 0.000 description 5
- 239000000470 constituent Substances 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- DNXNYEBMOSARMM-UHFFFAOYSA-N alumane;zirconium Chemical compound [AlH3].[Zr] DNXNYEBMOSARMM-UHFFFAOYSA-N 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- HZEWFHLRYVTOIW-UHFFFAOYSA-N [Ti].[Ni] Chemical compound [Ti].[Ni] HZEWFHLRYVTOIW-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 229910001000 nickel titanium Inorganic materials 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 229910001093 Zr alloy Inorganic materials 0.000 description 1
- ZGUQGPFMMTZGBQ-UHFFFAOYSA-N [Al].[Al].[Zr] Chemical compound [Al].[Al].[Zr] ZGUQGPFMMTZGBQ-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000003028 elevating effect Effects 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- PYLLWONICXJARP-UHFFFAOYSA-N manganese silicon Chemical compound [Si].[Mn] PYLLWONICXJARP-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
Definitions
- This invention relates to an improved zinc base alloy and a process for producing such an alloy. More particularly, the invention pertains to an alloy of this type which is characterized by outstanding wear resistance properties due to the presence of hard particles of an iron- Zirconium-aluminum alloy.
- the present application is a division of United States patent application Serial No. 520,148 which was filed on July 5, 1955.
- Zinc base alloys commercially used today for drawing dies and similar purposes usually possess inadequate wear properties for many requirements. It is therefore a principal object of the present invention to overcome this deficiency by providing a zinc base alloy characterized by greatly increased wear properties, high resistance to fracture, good castability and homogeneity. It is a further object of this invention to provide a drawing die formed of an inexpensive zinc base alloy which possesses high wear resistance, a low melting point and uniform shrinkage.
- a zinc alloy containing a small amount of dispersed particles of ironzirconium-aluminum alloy.
- the iron-zirconium-aluminum particles contain hard intermetallic compounds or phases of aluminum-Zirconium which are primarily responsible for the outstanding Wear resistance of the zinc base alloy.
- a zinc base alloy which contains small amounts of copper and additional aluminum, as Well as the aforementioned hard particles, is especially suitable for use as a drawing die.
- a small amount of magnesium also may be advantageously included in the alloy.
- the aluminum and copper are added to increase the tensile strength and hardness and to reduce the solidification temperature of the alloy.
- Magnesium is preferably included in the alloy to overcome the corrosive influence of any impurities which may be present in the alloy. It therefore promotes dimensional stability and prevents a decrease in the strength of the alloy on aging.
- the resultant material is a long-wearing, generally homogeneous alloy having good castability properties.
- the Wear resistance of a zinc base alloy may be improved by theinclusion of dispersed, hard particles of nickeltitanium in the alloy.
- iron-Zirconium-aluminum alloys do not contain any relatively critical nickel and hence are preferred in the event of a nickel shortage because of a national emergency or for other reasons.
- the average iron-zirconium-aluminum alloy is appreciably less expensive than typical nickel-titanium alloys.
- the aforementioned beneficial. properties are obtained to aparticularly high degree in a zinc base alloy containing aluminum, copper and magnesium by the inclusion therein of iron-zirconium-aluminum in the form of small particles which are generally uniformly dispersed throughout the zinc base alloy. As hereinafter more fully explained, these particles may be advantageously introduced into the zinc-rich melt in the form of a copper base intermediate alloy.
- the low melting point of the zinc base alloy eliminates the need for elaborate equipment in the alloying procedure, only a comparatively simple gasor oil-fired melting kettle being required.
- the uniform shrinkage characteristic of this alloy permits the exact size of castings to be predetermined with precision, eliminating the necessity for extensive use of profiling machines. Accordingly, the subject alloy is ideally suited for use as drawing dies since the processing of dies formed of this alloy is comparatively simple, requiring a minimum of equipment and labor. Cost is further reduced by the fact that this alloy can be remelted many times, permitting the material in obsolete dies to be almost entirely recovered.
- this type of zinc base alloy can be cast and the diversity of forms into which the molten alloy will flow make it a very desirable material for a variety of purposes. Furthermore, finished castings of this alloy can be produced comparatively quickly, making them available for production use within a relatively short time.
- the high wear resistance of the final zinc base alloy is due to the presence of the dispersed, hard particles of iron-zirconium-aluminum alloy.
- Hard compounds or phases are known to occur in the binary system of zirconium-aluminum, but these hard materials alone are generally unsuitable for inclusion in a cast zinc base alloy since their densities are lower than the density of the zincrich melt to which they are added. Particles of zirconiumaluminum therefore tend to float to the top of molten zinc base alloys and are of little value in applications where substantial homogeneity of the casting is required. Furthermore, certain of these phases will decompose or dissolve in molten Zinc and lose their identity.
- the present invention provides an alloy which has proper particle distribution, as well as optimum particle size, resulting in physical characteristics which satisfy all requirements for an outstanding tool alloy.
- a desirable zinc base drawing die alloy which possesses exceptional wear resistance is one consisting essentially of about 2% to aluminum, 0.5% to 5% copper, 1% to 3% hard particles of iron-zirconium-aluminum and the balance substantially all zinc.
- the inclusion of approximately 0.02% to 0.3% magnesium is beneficial to reduce the corrosive tendencies of impurities such. as lead, cadmium and tin.
- the zinc base alloy also may contain small amounts of silicon and other elements as incidental impurities.
- a zinc base alloy containing at least approximately 85% zinc has it wear resistance appreciably improved by the presence of the aforementioned hard iron-zirconiumaluminum particles.
- zinc base alloyf as used herein, is intended to encompass those alloys in which zinc is the major constituent and preferably constitutes at least 50% of the alloy.
- Wear resistance is a function of both the size and distribution of the hard iron-zirconium-alurninum particles. Since particle size and distribution are dependent on such factors as metal viscosity, solidification rates and methods of alloying, this invention also provides a preferred procedure for preparing the zinc base alloy. In the case of a drawing die, it is desirable to produce maximum Wear resistance without causing scoring of the part being drawn.
- the iron-zirconium-aluminum alloy can be initially prepared by melting together the three individual constituents. Commercially pure zirconium and aluminum, such as 28 aluminum, may be conveniently used. Alternatively, of course, commercially available zirconiumaluminum alloy may be added to molten iron to form the pre-alloy.
- the resultant pro-alloy may contain small amounts of other metals, such as manganese silicon, chromium, magnesium and nickel. Normally the maximum quantity of these metals would not exceed approximately 5% manganese, 2% silicon, 1% chromium, 1% magnesium, and 0.5 nickel. These percentages of the minor constituents are not critical in most instances, however, and are listed as examples only.
- iron-zirconium-aluminum pre-alloy does not readily dissolve in the zinc-rich melt, it is preferred to introduce these hard particles in the form of an intermediate alloy or hardener containing copper.
- the iron-zirconium-aluminum When the iron-zirconium-aluminum is added to molten copper, it is transformed substantially into the molten state and is absorbed by the molten copper.
- zirconium-aluminum suspended in the zinc as wearresistant particles of appropriate size. Agitation of the zinc-rich melt causes these particles to become generally uniformly dispersed through the melt, and the particles remain so dispersed in the solidified zinc base casting.
- the desired drawing die alloy composition is preferably obtained by melting substantially pure zinc and, after elevating the temperature of the molten zinc to between about 950 F. and 1075 d F., dissolving therein the solidification of the intermediate alloy, the solubility of k the iron-zirconium-aluminum is decreased and is therefore preferentially isolated as a network in the copperrich matrix.
- this hardener is preferably added to the zinc in the solid state. Since it is desirable to cast the copper base intermediate alloy in shapes in which the copper-rich matrix will dissolve most readily in the molten zinc-rich alloy, it is preferred to form castings having a high ratio of surface area to volume, such as fiat plates or thin sheets. Generally the formed ironzirconium-aluminum. particles have diameters in the order of about 0.001 inch. If the particles are much smaller than this, the wear resistance of the final zinc base alloy is not increased to the desired extent.
- the copper or copper-rich matrix is dissolved, leaving the relatively insoluble network of ironaluminum to be added except that which is contained in the copper-iron-zirconium-aluminum intermediate alloy.
- This addition of aluminum retards drossing of the zinc at higher temperatures and, if a cast iron melting pot is employed, it inhibits attack of the pot by the zinc-rich melt.
- an appropriate amount of the copper-iron-zirconium-aluminum hardening alloy is added in thesolid state, as hereinbefore indicated.
- the elevated temperature should be maintained until the aforementioned copper-rich matrix in this hardening alloy is entirely dissolved, the solution rate being increased by periodic agitation. After this solution is accomplished, we have found it desirable to lower the temperature of the melt to approximately 900 F. to 950 F.
- a suitable flux such as ammonium chloride, may then be added to remove dross from the melt.
- the magnesium is thereafter introduced, if it is to be included in the alloy, preferably by submerging it in the bath.
- the final alloy may then be cast to shape in suitable molds.
- the aluminum not included in the ironzirconium-aluminum alloy can be added either before or after addition of the intermediate alloy, the above alloying sequence has been found to be most satisfactory. Alternatively, a portion of this aluminum may be added prior to the introduction of the intermediate alloy and the remaining aluminum added after this alloy addition.
- the ironzirconium-aluminum alloy have a density which approximates that of the zinc-rich melt in order to prevent floatation or segregation of the iron-zirconium-aluminum particles.
- the density of zinc at its melting point is 6.92 grams per cc., and the addition of about 4% aluminum decreases the density of the resultant alloy to approxi mately 6.9 grams per cc. Therefore, in order to obtain proper distribution of the iron-zirconium-aluminum particles, it is desirable to form these particles of an alloy having a specific gravity of about 6.5 to 7.5 grams per cc.
- the density of iron is 7.87 grams per cc.
- an iron-zirconiumaluminum alloy consisting essentially of 68% iron, 20% zirconium and 12% aluminum provides excellent results.
- Such an alloy has a calculated density of about 6.99 grams per cc., which is slightly higher than the specific gravity of the aforementioned zinc-rich melt. Based on density requirements, therefore, the iron should constitute about 55% to of the iron-zirconiumaluminum alloy.
- the particles of this alloy may dissolve in the Zinc if the iron content is above approximately
- the wear resistance of a zinc base alloy may be substantially improved with an iron-zirconiurn-aluminum pre-alloy comprising approximately 12% to 25% zirconium, 8% to 20% aluminum and the balance iron.
- Such a pre-alloy produces particles of optimum size and density. In some instances, however, this pre-alloy may contain as little as 8% or as much as 30% zirconium, and the aluminum content may vary from about 5% to 25%.
- the iron-zirconium-aluminum pre-alloy When the iron-zirconium-aluminum pre-alloy is mixed with the molten copper, usually at a temperature of 2200 F. to 2700" F., it is preferred to form an intermediate alloy containing approximately 55% to 90% copper. If this alloy has a copper content less than 55% it is diflicult to place the copper-rich matrix of the copper-iron-zirconium-aluminum intermediate alloy in solution in the zincrlch melt. Therefore, a copper base alloy comprising about 1.5% to 11% zirconium, 0.8% to 8% aluminum,
- the intermediate alloy may constitute about 1% to 9% of the final alloy, although 3% to 6.5% is preferred.
- the intermediate alloy When such an intermediate alloy is added to a zinc-rich melt, it introduces into the final alloy approximately 0.35% to 26% iron, 0.1% to 0.8% zirconium and 0.06% to 0.5 aluminum in the form of iron-zirconium-aluminum particles and about 0.5 to 5% copper which is not combined with these particles.
- the ironzirconium-aluminum pre-alloy may be compounded by melting together the proper amounts of iron, zirconium and aluminum, preferably at a temperature of approximately 2900 F. to 3100 F.
- zirconium is a rather readily oxidizable and nitridable element
- a wear test using this apparatus was conducted in which the specimen load was increased during a five-hour period from zero load and automatically adjusted to produce a constant frictional load rather than a constant load normal to the wheel.
- This test included a ten minute run-in period in which only the weight of the specimen being tested and its holder bore against the wheel, a period of 1% hours to load the specimen to 500 pounds, a 30 minute period at 500 pounds to establish the frictional characteristics, and the balance of the five hours run with this established value of friction maintained constant. After each test any loosely adhering, deformed metal and burrs were removed from the wear test sample, and loss in weight values were used in comparing the wear resistance of the specimen.
- the zinc base alloy specimens formed from a zinc base alloy consisting essentially of 3.25% copper, 4% aluminum, 0.1% magnesium and the balance zinc showed an average weight loss of 0.4764 gram.
- a zinc base die alloy specimen of similar composition but containing the aforementioned preferred amounts of the iron-zirconium-aluminum particles lost an average of only approximately 0.0436 gram. The results of this test show how greatly the presence of dispersed particles of the hard iron-zirconium-aluminum alloy increases the wear resistance of zinc base alloys.
- the final alloy formed has been described as particularly suitable as a drawing die material, it also may be employed to considerable advantage in other applications in which high wear resistance, good castability, uniformity of properties throughout a cast section, good machinability, and anti-score properties are of importance.
- a pre-alloy for introducing hard iron-zirconiumaluminum particles to a zinc base alloy for imparting high wear resistance thereto said pre-alloy consisting essentially of about 55% to copper, 5% to 35% iron, 1.5% to 11% zirconium and 0.8% to 8% aluminum, a substantial proportion of said iron, zirconium and aluminum being present in the form of a network of iron-zirconium-aluminum in a copper-rich matrix of said pro-alloy.
- a copper base alloy comprising about 55% to 90% copper, 5% to 35% iron, 1.5% to 11% zirconium and 0.8% to 8% aluminum, a substantial proportion of said iron, zirconium and aluminum being present in the form of a hard network of at least one iron-zirconium-aluminum ternary compound in a copper-rich matrix of said copper base alloy.
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Description
United Sttes Paten COPPER BASE PREALLOY FOR ADDITION T ZINC Robert F. Thomson, Grosse Pointe Woods, and James C. Holzwarth, Birmingham, Mich.
No Drawing. Original application July 5, 1955, Serial No. 520,148. Divided and this application March 31, 1958, Serial No. 724,890
3 Claims. (Cl. 75-162) This invention relates to an improved zinc base alloy and a process for producing such an alloy. More particularly, the invention pertains to an alloy of this type which is characterized by outstanding wear resistance properties due to the presence of hard particles of an iron- Zirconium-aluminum alloy. The present application is a division of United States patent application Serial No. 520,148 which was filed on July 5, 1955.
Zinc base alloys commercially used today for drawing dies and similar purposes usually possess inadequate wear properties for many requirements. It is therefore a principal object of the present invention to overcome this deficiency by providing a zinc base alloy characterized by greatly increased wear properties, high resistance to fracture, good castability and homogeneity. It is a further object of this invention to provide a drawing die formed of an inexpensive zinc base alloy which possesses high wear resistance, a low melting point and uniform shrinkage.
These and other objects and advantages are attained in accordance with the present invention with a zinc alloy containing a small amount of dispersed particles of ironzirconium-aluminum alloy. The iron-zirconium-aluminum particles contain hard intermetallic compounds or phases of aluminum-Zirconium which are primarily responsible for the outstanding Wear resistance of the zinc base alloy.
in particular, we have found that a zinc base alloy which contains small amounts of copper and additional aluminum, as Well as the aforementioned hard particles, is especially suitable for use as a drawing die. A small amount of magnesium also may be advantageously included in the alloy. In this type of zinc base alloy the aluminum and copper are added to increase the tensile strength and hardness and to reduce the solidification temperature of the alloy. Magnesium is preferably included in the alloy to overcome the corrosive influence of any impurities which may be present in the alloy. It therefore promotes dimensional stability and prevents a decrease in the strength of the alloy on aging. The resultant material is a long-wearing, generally homogeneous alloy having good castability properties.
As disclosed in United States Patent No. 2,720,459, the Wear resistance of a zinc base alloy may be improved by theinclusion of dispersed, hard particles of nickeltitanium in the alloy. However, iron-Zirconium-aluminum alloys do not contain any relatively critical nickel and hence are preferred in the event of a nickel shortage because of a national emergency or for other reasons. Furthermore, the average iron-zirconium-aluminum alloy is appreciably less expensive than typical nickel-titanium alloys.
In accordance with the invention, therefore, the aforementioned beneficial. properties are obtained to aparticularly high degree in a zinc base alloy containing aluminum, copper and magnesium by the inclusion therein of iron-zirconium-aluminum in the form of small particles which are generally uniformly dispersed throughout the zinc base alloy. As hereinafter more fully explained, these particles may be advantageously introduced into the zinc-rich melt in the form of a copper base intermediate alloy.
The low melting point of the zinc base alloy eliminates the need for elaborate equipment in the alloying procedure, only a comparatively simple gasor oil-fired melting kettle being required. The uniform shrinkage characteristic of this alloy permits the exact size of castings to be predetermined with precision, eliminating the necessity for extensive use of profiling machines. Accordingly, the subject alloy is ideally suited for use as drawing dies since the processing of dies formed of this alloy is comparatively simple, requiring a minimum of equipment and labor. Cost is further reduced by the fact that this alloy can be remelted many times, permitting the material in obsolete dies to be almost entirely recovered.
In addition, the facility with which this type of zinc base alloy can be cast and the diversity of forms into which the molten alloy will flow make it a very desirable material for a variety of purposes. Furthermore, finished castings of this alloy can be produced comparatively quickly, making them available for production use within a relatively short time.
The high wear resistance of the final zinc base alloy is due to the presence of the dispersed, hard particles of iron-zirconium-aluminum alloy. Hard compounds or phases are known to occur in the binary system of zirconium-aluminum, but these hard materials alone are generally unsuitable for inclusion in a cast zinc base alloy since their densities are lower than the density of the zincrich melt to which they are added. Particles of zirconiumaluminum therefore tend to float to the top of molten zinc base alloys and are of little value in applications where substantial homogeneity of the casting is required. Furthermore, certain of these phases will decompose or dissolve in molten Zinc and lose their identity. However, we have found that these hard zirconium-aluminum compounds can be combined with iron and, with proper selection of compositions and alloying methods, the resultant iron-zirconium-aluminum alloy can be made to remain in suspension in the molten zinc base alloy as discreet hard particles which provide the final cast alloy with greatly increased wear resistance. These hard particles do not readily float or settle out of the zinc-rich melt since they have a specific gravity which closely approximates that of the zinc-rich melt.
Regardless of the exact chemical composition of the iron-zirconium-aluminum particles, their presence in the softer zinc base matrix material is responsible for the marked increase in Wear resistance, particularly with the type of wear experienced with dies used in drawing and forming operations. Hence the present invention provides an alloy which has proper particle distribution, as well as optimum particle size, resulting in physical characteristics which satisfy all requirements for an outstanding tool alloy.
Commercially satisfactory results may be obtained in accordance with our invention with a final zinc base alloy containing approximately 1% to 3% by weight of hard particles of iron-zirconium-aluminum alloy. However, the iron-zirconium-aluminum particles may be present in amounts as large as about 4%by weight, and in some instances a noticeable improvement in wear resistance results when these particles constitute as little as about 0.5% of the zinc base alloy. If the alloy contains more than approximately 4% of these particles, the castability of the alloy is impaired and its cost becomes excessive. Hence, a desirable zinc base drawing die alloy which possesses exceptional wear resistance is one consisting essentially of about 2% to aluminum, 0.5% to 5% copper, 1% to 3% hard particles of iron-zirconium-aluminum and the balance substantially all zinc. The inclusion of approximately 0.02% to 0.3% magnesium is beneficial to reduce the corrosive tendencies of impurities such. as lead, cadmium and tin. Itwill be understood, of course, that the zinc base alloy also may contain small amounts of silicon and other elements as incidental impurities.
Thus it can be seen that in accordance with our invention a zinc base alloy containing at least approximately 85% zinc has it wear resistance appreciably improved by the presence of the aforementioned hard iron-zirconiumaluminum particles. It will be understood, however, that the term zinc base alloyf as used herein, is intended to encompass those alloys in which zinc is the major constituent and preferably constitutes at least 50% of the alloy.
More specifically, we have obtained outstanding wear characteristics in a cast alloy consisting essentially of 87% to 93% zinc, 3% to 5% aluminum, 2% to 3.5% copper, 0.05% to 0.2% magnesium, and 1% to 3% iron-zirconium-aluminum alloy in the form of dispersed hard particles. An alloy consisting of approximately 4% aluminum, 0.15% magnesium, 3.25% copper, 1.5% ironzirconium-aluminum and the balance Zinc plus incidental impurities appears to possess optimum castability and wear resistance properties.
Wear resistance, of course, is a function of both the size and distribution of the hard iron-zirconium-alurninum particles. Since particle size and distribution are dependent on such factors as metal viscosity, solidification rates and methods of alloying, this invention also provides a preferred procedure for preparing the zinc base alloy. In the case of a drawing die, it is desirable to produce maximum Wear resistance without causing scoring of the part being drawn.
The iron-zirconium-aluminum alloy can be initially prepared by melting together the three individual constituents. Commercially pure zirconium and aluminum, such as 28 aluminum, may be conveniently used. Alternatively, of course, commercially available zirconiumaluminum alloy may be added to molten iron to form the pre-alloy. The resultant pro-alloy may contain small amounts of other metals, such as manganese silicon, chromium, magnesium and nickel. Normally the maximum quantity of these metals would not exceed approximately 5% manganese, 2% silicon, 1% chromium, 1% magnesium, and 0.5 nickel. These percentages of the minor constituents are not critical in most instances, however, and are listed as examples only.
Inasmuch as the iron-zirconium-aluminum pre-alloy does not readily dissolve in the zinc-rich melt, it is preferred to introduce these hard particles in the form of an intermediate alloy or hardener containing copper. When the iron-zirconium-aluminum is added to molten copper, it is transformed substantially into the molten state and is absorbed by the molten copper. During 4 zirconium-aluminum suspended in the zinc as wearresistant particles of appropriate size. Agitation of the zinc-rich melt causes these particles to become generally uniformly dispersed through the melt, and the particles remain so dispersed in the solidified zinc base casting.
The desired drawing die alloy composition is preferably obtained by melting substantially pure zinc and, after elevating the temperature of the molten zinc to between about 950 F. and 1075 d F., dissolving therein the solidification of the intermediate alloy, the solubility of k the iron-zirconium-aluminum is decreased and is therefore preferentially isolated as a network in the copperrich matrix. In order to form long-wearing particles of suitable size, this hardener is preferably added to the zinc in the solid state. Since it is desirable to cast the copper base intermediate alloy in shapes in which the copper-rich matrix will dissolve most readily in the molten zinc-rich alloy, it is preferred to form castings having a high ratio of surface area to volume, such as fiat plates or thin sheets. Generally the formed ironzirconium-aluminum. particles have diameters in the order of about 0.001 inch. If the particles are much smaller than this, the wear resistance of the final zinc base alloy is not increased to the desired extent.
Upon introduction of the intermediate alloy to the zinc-rich melt, the copper or copper-rich matrix is dissolved, leaving the relatively insoluble network of ironaluminum to be added except that which is contained in the copper-iron-zirconium-aluminum intermediate alloy. This addition of aluminum retards drossing of the zinc at higher temperatures and, if a cast iron melting pot is employed, it inhibits attack of the pot by the zinc-rich melt. After further raising the temperature of the melt to approximately 12100 F.'to 1300 R, an appropriate amount of the copper-iron-zirconium-aluminum hardening alloy is added in thesolid state, as hereinbefore indicated. The elevated temperature should be maintained until the aforementioned copper-rich matrix in this hardening alloy is entirely dissolved, the solution rate being increased by periodic agitation. After this solution is accomplished, we have found it desirable to lower the temperature of the melt to approximately 900 F. to 950 F. A suitable flux, such as ammonium chloride, may then be added to remove dross from the melt. The magnesium is thereafter introduced, if it is to be included in the alloy, preferably by submerging it in the bath. The final alloy may then be cast to shape in suitable molds.
Although the aluminum not included in the ironzirconium-aluminum alloy can be added either before or after addition of the intermediate alloy, the above alloying sequence has been found to be most satisfactory. Alternatively, a portion of this aluminum may be added prior to the introduction of the intermediate alloy and the remaining aluminum added after this alloy addition.
As hereinbefore explained, it is desirable that the ironzirconium-aluminum alloy have a density which approximates that of the zinc-rich melt in order to prevent floatation or segregation of the iron-zirconium-aluminum particles. The density of zinc at its melting point is 6.92 grams per cc., and the addition of about 4% aluminum decreases the density of the resultant alloy to approxi mately 6.9 grams per cc. Therefore, in order to obtain proper distribution of the iron-zirconium-aluminum particles, it is desirable to form these particles of an alloy having a specific gravity of about 6.5 to 7.5 grams per cc. The density of iron is 7.87 grams per cc. and the density of aluminum is 2.7 grams per cc., while the density of commercially available zirconium is about 6.5 grams per cc. Hence, we have found that an iron-zirconiumaluminum alloy consisting essentially of 68% iron, 20% zirconium and 12% aluminum provides excellent results. Such an alloy has a calculated density of about 6.99 grams per cc., which is slightly higher than the specific gravity of the aforementioned zinc-rich melt. Based on density requirements, therefore, the iron should constitute about 55% to of the iron-zirconiumaluminum alloy. Moreover, there appears to be a tendency for the particles of this alloy to dissolve in the Zinc if the iron content is above approximately We prefer to have a ratio of zirconium to aluminum in the iron-zirconium-aluminum alloy of about 1.6 to l, but an appreciable variation in the relative amounts of these three constituents is permissible. Thus We have found that the wear resistance of a zinc base alloy may be substantially improved with an iron-zirconiurn-aluminum pre-alloy comprising approximately 12% to 25% zirconium, 8% to 20% aluminum and the balance iron. Such a pre-alloy produces particles of optimum size and density. In some instances, however, this pre-alloy may contain as little as 8% or as much as 30% zirconium, and the aluminum content may vary from about 5% to 25%.
When the iron-zirconium-aluminum pre-alloy is mixed with the molten copper, usually at a temperature of 2200 F. to 2700" F., it is preferred to form an intermediate alloy containing approximately 55% to 90% copper. If this alloy has a copper content less than 55% it is diflicult to place the copper-rich matrix of the copper-iron-zirconium-aluminum intermediate alloy in solution in the zincrlch melt. Therefore, a copper base alloy comprising about 1.5% to 11% zirconium, 0.8% to 8% aluminum,
5% to 35% iron and the balance copper isaplpropriate for use in carrying out the present invention. In order to provide a zinc base alloy with approximately 0.5% to 4% iron-zirconium-aluminum particles, the intermediate alloy may constitute about 1% to 9% of the final alloy, although 3% to 6.5% is preferred. When such an intermediate alloy is added to a zinc-rich melt, it introduces into the final alloy approximately 0.35% to 26% iron, 0.1% to 0.8% zirconium and 0.06% to 0.5 aluminum in the form of iron-zirconium-aluminum particles and about 0.5 to 5% copper which is not combined with these particles.
Since the hard particles result principally from the combination of aluminum and zirconium and are formed during the preparation of the pre-alloy, the alloying procedure employed in forming the hardener is of importance in achieving optimum results. Accordingly, the ironzirconium-aluminum pre-alloy may be compounded by melting together the proper amounts of iron, zirconium and aluminum, preferably at a temperature of approximately 2900 F. to 3100 F. Inasmuch as zirconium is a rather readily oxidizable and nitridable element, it is desirable to use an inert gas as the melting atmosphere. We have obtained most satisfactory melting and high zirconium recovery using an induction furnace under an argon atmosphere.
It will be noted that it is necessary to form particles of iron-zirconium-aluminum in order to obtain high wear and score resistance in accordance with the invention. Merely adding the iron, zirconium and aluminum separately to the zinc-rich melt, even if these constitutents are introduced in the aforementioned preferred proportions, does not form these hard particles or provide the necessary wear resistance. It is the alloy of iron, zirconium and aluminum, rather than the individual elements, which contributes the desirable properties of wear and score resistance to the final zinc base alloy.
Wear tests were conducted to compare zinc base alloys formed in accordance with our invention with the same material devoid of iron-zirconium-aluminum particles. Samples 1% inches wide and /8 inch high were prepared from the cast zinc base alloys to be tested, and each specimen was machined at one edge to prepare a A; inch by 1% inch rubbing surface. The specimens were next successively locked in a fixture of a wear test machine and placed in contact with a rotating smooth-surfaced wheel of low carbon steel having a face width of one inch. Increased wear resistance was measured by decreased weight loss in grams.
A wear test using this apparatus was conducted in which the specimen load was increased during a five-hour period from zero load and automatically adjusted to produce a constant frictional load rather than a constant load normal to the wheel. This test included a ten minute run-in period in which only the weight of the specimen being tested and its holder bore against the wheel, a period of 1% hours to load the specimen to 500 pounds, a 30 minute period at 500 pounds to establish the frictional characteristics, and the balance of the five hours run with this established value of friction maintained constant. After each test any loosely adhering, deformed metal and burrs were removed from the wear test sample, and loss in weight values were used in comparing the wear resistance of the specimen.
At the end of the test period the zinc base alloy specimens formed from a zinc base alloy consisting essentially of 3.25% copper, 4% aluminum, 0.1% magnesium and the balance zinc showed an average weight loss of 0.4764 gram. On the other hand, a zinc base die alloy specimen of similar composition but containing the aforementioned preferred amounts of the iron-zirconium-aluminum particles lost an average of only approximately 0.0436 gram. The results of this test show how greatly the presence of dispersed particles of the hard iron-zirconium-aluminum alloy increases the wear resistance of zinc base alloys.
Although the final alloy formed has been described as particularly suitable as a drawing die material, it also may be employed to considerable advantage in other applications in which high wear resistance, good castability, uniformity of properties throughout a cast section, good machinability, and anti-score properties are of importance.
While we have set forth herein specific examples of zinc base alloys possessing high wear resistance characteristics due to the presence of hard particles of iron-zirconiumaluminum, it is not intended to restrict the invention to any specific zinc base alloy. We believe that we are the first to discover the value of adding these particles to zinc base alloys generally, and the invention is not to be restricted except as defined in the following claims.
We claim: 5
1. A pre-alloy for introducing hard iron-zirconiumaluminum particles to a zinc base alloy for imparting high wear resistance thereto, said pre-alloy consisting essentially of about 55% to copper, 5% to 35% iron, 1.5% to 11% zirconium and 0.8% to 8% aluminum, a substantial proportion of said iron, zirconium and aluminum being present in the form of a network of iron-zirconium-aluminum in a copper-rich matrix of said pro-alloy.
2. The process of preparing an alloy which comprises dissolving zirconium and aluminum in molten iron under an inert atmosphere to form a ferrous base pre-alloy, and thereafter dissolving said pre-alloy in molten copper, said metals being added in proportions to provide an alloy consisting essentially of 5% to 35 iron, 1.5 to 11% zirconium, 0.8% to 8% aluminum and the balance sub stantially all copper.
3. A copper base alloy comprising about 55% to 90% copper, 5% to 35% iron, 1.5% to 11% zirconium and 0.8% to 8% aluminum, a substantial proportion of said iron, zirconium and aluminum being present in the form of a hard network of at least one iron-zirconium-aluminum ternary compound in a copper-rich matrix of said copper base alloy.
References Cited in the file of this patent UNITED STATES PATENTS 2,720,459 Holzwarth Oct. 11, 1955 2,810,641 Roberts Oct. 22, 1957 FOREIGN PATENTS 333,442 Great Britain Aug. 14, 1930 440,480 Great Britain Dec. 19, 1935 512,142 Great Britain Aug. 30, 1939 OTHER REFERENCES Alloys of Copper and Iron, Smith and Palmer, Trans. AIME, vol. 188, December 1950, Journal of Metals, pages 1486-1499.
UNITED STATES PATENT OFFICE CERTHHCATE OFCORRECTHNV Patent No. 2 924 517 February 9 1960 Robert F. Thomson et al.
In the grant, lines 1 and 2 for "Robert F. Thomson, of Grosse Pointe Woods, and James C. Holzwarth, of Birmingham, Michigan read Robert F. Thomson, of Grosse Pointe Woods and James Cm Holzwarth, of Birmingham, Michigan, assignors to General Motors Corporation, of Detroit, Michigan a corporation of Delaware, line 11 for "Robert F. Thomson and James C. Holzwarth, their heirs" read General Motors Corporation, its successors in the heading to the printed specification, lines 4 and 5, for "Robert F. Thomson, Grosse Pointe Woods and James C. Holzwarth, Birmingham Mich,fl read Robert F, Thomson Grosse Pointe Woods, and James Ci Holzwarth, Birmingham, Mich;, assignors to General Motors Corporation, Detroit, Mich., a corporation of Delaware (SEAL) Attest:
KARL H. AXLINE ROBERT C. WATSON Attesting Officer Commissioner of Patents
Claims (1)
1. A PRE-ALLOY FOR INTRODUCING HARD IRON-ZIRCONIUMALUMINUM PARTICLES TO A ZINC BASE ALLOY FOR INPARTING HIGH WEAR RESISTANCE THERETO, SAID PRE-ALLOY CONSISTING ESSENTIALLY OF ABOUT 55% TO 90% COPPER, 5% TO 35% IRON, 1.5% TO 11% ZIRCONIUM AND 0.8% TO 8% ALUMINUM, A SUBSTIANTIALLY PROPORATION OF SAID IRON, ZIRCONIUM AND ALUMINUM BEING PRESENT IN THE FORM OF A NETWORK OF IRON-ZIRCONIUM-ALUMINUM IN A COPPER-RICH MATRIX OF SAID-ALLOY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US724890A US2924517A (en) | 1955-07-05 | 1958-03-31 | Copper base prealloy for addition to zinc |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US520148A US2912324A (en) | 1955-07-05 | 1955-07-05 | Highly wear-resistant zinc base alloy and method of making same |
| US724890A US2924517A (en) | 1955-07-05 | 1958-03-31 | Copper base prealloy for addition to zinc |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2924517A true US2924517A (en) | 1960-02-09 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US724890A Expired - Lifetime US2924517A (en) | 1955-07-05 | 1958-03-31 | Copper base prealloy for addition to zinc |
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| US (1) | US2924517A (en) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB333442A (en) * | 1929-10-02 | 1930-08-14 | Gustav Baertges | Improvements relating to the production of bronze |
| GB440480A (en) * | 1933-04-13 | 1935-12-19 | William Guertler | Improvements in or relating to constructional parts, or articles, manufactured from copper-zirconium alloys |
| GB512142A (en) * | 1937-11-19 | 1939-08-30 | Mallory & Co Inc P R | Improvements in copper base alloys |
| US2720459A (en) * | 1950-08-08 | 1955-10-11 | Gen Motors Corp | Highly wear-resistant zinc base alloy |
| US2810641A (en) * | 1954-12-22 | 1957-10-22 | Iii John S Roberts | Precipitation hardenable copper, nickel, aluminum, zirconium alloys |
-
1958
- 1958-03-31 US US724890A patent/US2924517A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB333442A (en) * | 1929-10-02 | 1930-08-14 | Gustav Baertges | Improvements relating to the production of bronze |
| GB440480A (en) * | 1933-04-13 | 1935-12-19 | William Guertler | Improvements in or relating to constructional parts, or articles, manufactured from copper-zirconium alloys |
| GB512142A (en) * | 1937-11-19 | 1939-08-30 | Mallory & Co Inc P R | Improvements in copper base alloys |
| US2720459A (en) * | 1950-08-08 | 1955-10-11 | Gen Motors Corp | Highly wear-resistant zinc base alloy |
| US2810641A (en) * | 1954-12-22 | 1957-10-22 | Iii John S Roberts | Precipitation hardenable copper, nickel, aluminum, zirconium alloys |
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