US3674448A - Anodic aluminum material and articles and composite articles comprising the material - Google Patents

Anodic aluminum material and articles and composite articles comprising the material Download PDF

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US3674448A
US3674448A US818145A US3674448DA US3674448A US 3674448 A US3674448 A US 3674448A US 818145 A US818145 A US 818145A US 3674448D A US3674448D A US 3674448DA US 3674448 A US3674448 A US 3674448A
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potential
cladding
aluminum
core
magnesium
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Robert H Brown
William A Anderson
William King
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Howmet Aerospace Inc
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/10Alloys based on aluminium with zinc as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F13/00Inhibiting corrosion of metals by anodic or cathodic protection
    • C23F13/02Inhibiting corrosion of metals by anodic or cathodic protection cathodic; Selection of conditions, parameters or procedures for cathodic protection, e.g. of electrical conditions
    • C23F13/06Constructional parts, or assemblies of cathodic-protection apparatus
    • C23F13/08Electrodes specially adapted for inhibiting corrosion by cathodic protection; Manufacture thereof; Conducting electric current thereto
    • C23F13/12Electrodes characterised by the material
    • C23F13/14Material for sacrificial anodes
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9265Special properties
    • Y10S428/933Sacrificial component
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12736Al-base component
    • Y10T428/12764Next to Al-base component

Definitions

  • An article comprising an anode material composed of a solution heat treatable and precipitation hardenable aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and a maximum of 0.25% copper and a maximum of 0.25% chromium, as impurities, the member exhibiting a stable solution potential upon exposure to varying thermal conditions.
  • a composite having a cladding composed of the material and a heat treatable aluminum alloy core.
  • an article composed of an aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and a maximum of 0.25% copper and a maximum of 0.25% chromium, as impurities.
  • the percentages are all by weight.
  • Articles fashioned from this alloy will exhibit upon exposure to varying thermal conditions a very stable electrolytic potential which does not vary by more than 50 mv. even though the temperature, time at temperature and other factors may be varied from one instance to another. Because the alloy is precipitation hardenable, it exhibits substantial strength typified by strength levels of 35 to over 50 k.s.i.
  • the silicon content must amount to at least 0.45 times the magnesium content. This assures that the desired stable solution potential will be achieved in each case.
  • the silicon content amount to 1 to 2 times the magnesium content. From the standpoint of improved strength, it is further preferred that manganese be included in an amount of 0.1 to 0.75%. Where higher levels of electrolytic potential are desired, for instance, levels consistently over 980 mv., the zinc content should be 3.5 to 8%.
  • a core material most highly suited is one of the alloy system usually designated the Al-Zn-Mg-Cu system.
  • This type of alloy carries the Aluminum Association Registration designation 7XXX and these alloys contain up to about 3 to 9% Zn, 1 to 3% Mg, copper in an amount of up to 3% together with additions of Cr, Mn and other elements.
  • Specific examples of these alloys include the following nominal compositions:
  • 7075 5.6 Zn, 2.5 Mg, 1.6 Cu, 0.3 Cr, bal.
  • A1 7079 4.3 Zn, 3.3 Mg, 0.6 Cu, 0.2 Mn, 0.2 Cr, bal. Al
  • the 7XXX type of alloy is known to exhibit high strength after solution heat treatment and precipitation hardening although it is also known that in some cases it is advisable to provide cathodic protection by means of an anodic cladding to which purpose the invention is especially suited.
  • the invention contemplates use of the improved anodic material as a cladding on a 7XXX aluminum alloy, in a broader sense, the improved anodic material should be useful with other heat treatable aluminimum cores and it is not necessarily intended to limit the invention to the use of a 7XXX core.
  • the solution potential of the core will most often vary from about 780 to about 850 mv. after precipitation hardening and the improved material provides suitable cathodic protection for such.
  • the articles can be manufactured by more or less stand ard techniques. Accordingly, an alloy of proper composition is cast into an ingot as by continuous casting and the ingot broken down by hot or cold working or both. Suitable working operations would include rolling, extruding, drawing and the like.
  • the core and cladding materials are separately processed as sheet or plate and then hot rolled together to provide a metallurgically bonded composite laminate.
  • the cladding may suitably constitute about 3 to of the total composite thickness.
  • Articles produced from the improved material may have their strength improved by solution heat treatment and precipitation hardening.
  • Solution heat treatment may be eifected by heating to a temperature of 825 F., or preferably a somewhat higher temperature of about 870 to 970 F. or more. Where the highest strength is desired, the solution heat treatment temperature should be at least 950 F.
  • the article is maintained at solution heat treating temperature for a period of time sufficient to take into solution substantially all the soluble alloy constituents. This time varies from case to case depending on the relative size of the article and the heating equipment employed and will generally vary from a matter of several minutes to several hours. Where the article is a composite article, the solution heat treatment time and temperature may be fixed by the particular core material utilized and the improved materials solution potential stability is especially desirable in such a case.
  • the article is quenched as by cold water immersion and then subjected to a precipitation hardening treatment wherein it is heated to a temperature of up to 400 F., but which generally ranges from 200' to 375 F., for varying durations depending on the exact physical and corrosion properties needed.
  • the precipitation hardening conditions may be fixed by the particular core material employed and again the stable solution potential of the improved anodic material is especially useful.
  • prior heat treatable anode compositions normally exhibit widely varying electrolytic potential levels in response to varying solution heat treatment and precipitation hardening treatments whereas the improved material exhibits highly stable solution potential levels. This permits the selection of thermal treatment conditions without regard for any sensitivity on the part of the cladding.
  • Composition A is clearly outside the practice of the invention and exemplifies an aluminumzinc-magnesium alloy which, in turn, typifies prior heat treatable aluminum alloys having an anodic electrolytic potential. Even though the alloy constituents, Zn, Mg and Si, broadly speaking, can be viewed as present within the ranges claimed herein, Composition B is nonetheless outside the invention as the ratio of its Si to Mg content amounts to only 0.38 which is less than the 0.45 level set out as essential in the practice of the invention. Composition C is within the practice of the invention with respect to the Zn, Mg and Si contents along with the silicon to magnesium ratio which is slightly over 0.62. Several plates of each composition were solution heat treated for two hours at two different temperatures.
  • the anode potential be 100 mv. more anodic than the material being protected, this potential diiference being a common value often chosen in the industry, it can be seen that variations of 93 to 96 mv. can render positive assurance of this difference quite difiicult. It is apparent that the comparatively minuscule potential variation associated with the practice of the invention minimizes this problem.
  • the improved material exhibits substantial strength especially when solution heat treated at a temperature of over 950 F. In such cases, the tensile strength is over 45 K.s.i. regardless of the thermal treatment.
  • An aluminum anode composed of a solution heat treatable and precipitation hardenable aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and a maximum of 0.25% copper and a maximum of 0.25% chromium, as impurities, said alloy article exhibiting, when subjected to a thermal exposure, a stable solution potential such that it does not vary by more than 50 mv. irrespective of the conditions of the thermal exposure.
  • An article comprising a clad composite having a core and a cladding, said cladding being anodic to said core thereby to cathodically protect the core, said core and cladding each being composed of a heat treatable and precipitation hardenable aluminum base alloy, said cladding being composed of an aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and impurities with a maximum of 0.25 copper and a maximum of 0.25 chromium as impurities, said core being composed of an aluminum base alloy consisting essentially of 3 to 9% zinc, 0.5 to 3% magnesium, and copper present in an amount of up to 3%, the balance being aluminum and incidental elements and impurities, said core and cladding being adapted to common solution heat treatment and precipitation hardening treatments, said core exhibiting, after said treatments, a solution potential of from about 780 to about 850 m
  • An article comprising a clad composite having a core and a cladding, said cladding being anodic to said core thereby to cathodically protect the core, said core and cladding each being composed of a heat treatable and precipitation hardenable aluminum base alloys, said cladding being composed of an aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and impurities with a maximum of 0.25% copper and a maximum of 0.25% chromium as impurities, said core and cladding being adapted to common solution heat treatment and precipitation hardening treatments, said core exhibiting, after said treatments, a solution potential of from about 780 to about 850 mv. and said cladding exhibiting, after said treatments, a stable solution potential which does not vary by more than 50 mv. irrespective of the particular time and temperature employed in said treatments.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Prevention Of Electric Corrosion (AREA)
  • Laminated Bodies (AREA)

Abstract

AN ARTICLE COMPRISING AN ANODE MATERIAL COMPOSED OF A SOLUTION HEAT TREATABLE AND PRECIPITATION HARDENABLE ALUMINUM BASE ALLOY CONSISTING ESSENTIALLY OF 2 TO 8% ZINC, 0.5 TO 2% MAGNESIUM, 0.3 TO 2% SILICON, THE SILICON CONTENT AMOUNTING TO AT LEAST 0.45 TIMES THE MAGNESIUM CONTENT, THE BALANCE BEING ALUMINUM AND INCIDENTAL ELEMENTS AND A MAXIMUM OF 0.25% COPPER AND A MAXIMUM OF 0.25% CHROMIUM, AS IMPURITIES, THE MEMBER EXHIBITING A STABLE SOLUTION POTENTIAL UPON EXPOSURE TO VARYING THERMAL CONDITIONS. ALSO CONTEMPLATED IS A COMPOSITE HAVING A CLADDING COMPOSED OF THE MATERIAL AND A HEAT TREATABLE ALUMINUM ALLOY CORE.

Description

United States Patent AN ODIC ALUMINUM MATERIAL AND ARTICLES AND COMPOSITE ARTICLES COMPRISING THE MATERIAL Robert H. Brown, Natrona Heights, William A. Anderson, Pittsburgh, and William King, Lower Burrell, Pa., assignors to Aluminum Company of America, Pittsburgh, Pa. No Drawing. Filed Apr. 21, 1969, Ser. No. 818,145
Int. Cl. B23p 3/02 US. Cl. 29197.5 9 Claims ABSTRACT OF THE DISCLOSURE An article comprising an anode material composed of a solution heat treatable and precipitation hardenable aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and a maximum of 0.25% copper and a maximum of 0.25% chromium, as impurities, the member exhibiting a stable solution potential upon exposure to varying thermal conditions. Also contemplated is a composite having a cladding composed of the material and a heat treatable aluminum alloy core.
BACKGROUND OF THE INVENTION There is an increasing need for aluminum materials having a relatively high anodic solution potential together with substantial strength. Such materials are useful to provide cathodic protection to structural members fashioned from other aluminous materials and are often more useful if they can be imparted with substantial strength so as to be suitable for bearing loads. One such application is where the anodic material serves as a protective cladding in a composite having a heat treatable core. Accordingly, aluminum alloy materials have been proposed which have relatively anodic electrolytic potentials and which are precipitation hardenable, by which is meant artificially ageable, which materials are useful in providing anodes which can bear loads. However, these materials are marked by variations in solution potential upon thermal exposures such as encountered in precipitation hardening treatments and even such as encountered in actual service. For example, an aluminum alloy containing zinc and magnesium and generally having a suitable anodic electrolytic potential will be observed to exhibit widely varying solution potential values varying over a range of up to 100 mv. and even more in response to varying aging or other thermal exposure conditions. In the case of a composite, the desired extent of the difference in solution potential between cladding and core can vary from one application to another although a difference of about 100 mv. is often desired. However, in such a system, it is quite apparent that where the solution potential of the cladding can vary up to 100 mv. because of differing thermal exposures, it becomes quite difiicult to assure any desired degree of cathodic protection. In addition, some core compositions require that the cladding solution potential be much greater than the core potential, there being some applications where a difference of 175 mv. is not sufficient. When it is noted that the total span in solution potential bracketing aluminum and all its commercial alloys amounts to about only 300 mv., it is quite apparent that fluctuations approaching 100 mv. can be extremely troublesome. As an example of thermal conditions encountered in service, in an automobile radiator an aluminum member could easily encounter a temperature considerably exceeding 170 F. and the precipitation 3,674,448 Patented July 4, 1972 ice hardenable aluminum anode materials proposed to date exhibit differences in electrolytic potential upon such exposures which are often considered unacceptably wide. Thus, the extent of the variations in potential renders it ditlicult to properly balance a dual alloy system from the standpoint of cathodic protection and an anodic material having a thermally stable solution potential would be highly desirable.
STATEMENT OF THE INVENTION In accordance with the invention, there is provided a strong solution heat treatable and precipitation hardenable aluminum alloy article which exhibits a very stable solution potential which will not vary by more than 50 mv. regardless of any variations in thermal exposure which might occur from situation to situation during thermal treatments such as precipitation hardening treatments or during service.
The foregoing advantages are achieved by providing an article composed of an aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and a maximum of 0.25% copper and a maximum of 0.25% chromium, as impurities. The percentages are all by weight. Articles fashioned from this alloy will exhibit upon exposure to varying thermal conditions a very stable electrolytic potential which does not vary by more than 50 mv. even though the temperature, time at temperature and other factors may be varied from one instance to another. Because the alloy is precipitation hardenable, it exhibits substantial strength typified by strength levels of 35 to over 50 k.s.i. tensile and 25 to over 40 k.s.i. yield strength. In practicing the invention, it is essential that, as indicated above, the silicon content must amount to at least 0.45 times the magnesium content. This assures that the desired stable solution potential will be achieved in each case. In order to further assure such and to further improve the strength of the material, it is preferred that the silicon content amount to 1 to 2 times the magnesium content. From the standpoint of improved strength, it is further preferred that manganese be included in an amount of 0.1 to 0.75%. Where higher levels of electrolytic potential are desired, for instance, levels consistently over 980 mv., the zinc content should be 3.5 to 8%.
In the case of a composite, a core material most highly suited is one of the alloy system usually designated the Al-Zn-Mg-Cu system. This type of alloy carries the Aluminum Association Registration designation 7XXX and these alloys contain up to about 3 to 9% Zn, 1 to 3% Mg, copper in an amount of up to 3% together with additions of Cr, Mn and other elements. Specific examples of these alloys include the following nominal compositions:
7075: 5.6 Zn, 2.5 Mg, 1.6 Cu, 0.3 Cr, bal. A1 7079: 4.3 Zn, 3.3 Mg, 0.6 Cu, 0.2 Mn, 0.2 Cr, bal. Al
The 7XXX type of alloy is known to exhibit high strength after solution heat treatment and precipitation hardening although it is also known that in some cases it is advisable to provide cathodic protection by means of an anodic cladding to which purpose the invention is especially suited. However, while the invention contemplates use of the improved anodic material as a cladding on a 7XXX aluminum alloy, in a broader sense, the improved anodic material should be useful with other heat treatable aluminimum cores and it is not necessarily intended to limit the invention to the use of a 7XXX core. In any event, the solution potential of the core will most often vary from about 780 to about 850 mv. after precipitation hardening and the improved material provides suitable cathodic protection for such.
The articles can be manufactured by more or less stand ard techniques. Accordingly, an alloy of proper composition is cast into an ingot as by continuous casting and the ingot broken down by hot or cold working or both. Suitable working operations would include rolling, extruding, drawing and the like.
In the case of a composite which may be sheet, the core and cladding materials are separately processed as sheet or plate and then hot rolled together to provide a metallurgically bonded composite laminate. In such rolled composites, the cladding may suitably constitute about 3 to of the total composite thickness. In some cases, especially where the core contains magnesium, it may be desirable to provide an interliner, intermediate the core and cladding and containing little or no magnesium, to assure a quality bond. Such has proven useful in producing composites utilizing the improved anode material with 7XXX type cores.
Articles produced from the improved material may have their strength improved by solution heat treatment and precipitation hardening. Solution heat treatment may be eifected by heating to a temperature of 825 F., or preferably a somewhat higher temperature of about 870 to 970 F. or more. Where the highest strength is desired, the solution heat treatment temperature should be at least 950 F. The article is maintained at solution heat treating temperature for a period of time sufficient to take into solution substantially all the soluble alloy constituents. This time varies from case to case depending on the relative size of the article and the heating equipment employed and will generally vary from a matter of several minutes to several hours. Where the article is a composite article, the solution heat treatment time and temperature may be fixed by the particular core material utilized and the improved materials solution potential stability is especially desirable in such a case.
After the solution heat treatment, the article is quenched as by cold water immersion and then subjected to a precipitation hardening treatment wherein it is heated to a temperature of up to 400 F., but which generally ranges from 200' to 375 F., for varying durations depending on the exact physical and corrosion properties needed. In the case of a composite, the precipitation hardening conditions may be fixed by the particular core material employed and again the stable solution potential of the improved anodic material is especially useful. As indicated earlier, prior heat treatable anode compositions normally exhibit widely varying electrolytic potential levels in response to varying solution heat treatment and precipitation hardening treatments whereas the improved material exhibits highly stable solution potential levels. This permits the selection of thermal treatment conditions without regard for any sensitivity on the part of the cladding.
In order to demonstrate the improvement derived from practicing the invention, the following examples proceed:
Example 1 TABLE I {Anodic alloy compositions] Composition:
In the above list, Composition A is clearly outside the practice of the invention and exemplifies an aluminumzinc-magnesium alloy which, in turn, typifies prior heat treatable aluminum alloys having an anodic electrolytic potential. Even though the alloy constituents, Zn, Mg and Si, broadly speaking, can be viewed as present within the ranges claimed herein, Composition B is nonetheless outside the invention as the ratio of its Si to Mg content amounts to only 0.38 which is less than the 0.45 level set out as essential in the practice of the invention. Composition C is within the practice of the invention with respect to the Zn, Mg and Si contents along with the silicon to magnesium ratio which is slightly over 0.62. Several plates of each composition were solution heat treated for two hours at two different temperatures. The plates were quenched by immersion in cold water and then precipitation hardened under varying conditions according to Table II. Oneeighth inch diameter short transverse, that is, across the 2 inch plate thickness, specimens were removed and tested for tensile properties. In addition, electrolytic potential measurements were made by measuring the specimens against a 0.1 N calomel electrode in 1.0 N NaCl plus 0.3% H 0 electrolyte, a procedure commonly used in the aluminum alloy art for such measurements. The results of these measurements are set forth in Tables III to V which set out the tensile and yield strength (TS. and Y.S.) together with the elongation in 2 inches and the solution potential (Pot) for each of the compositions in Table I under the seventeen diife'rent conditions of thermal treatment described in Table II.
Referring to Table III and Composition A, it can be seen that the different thermal treatments result in widely varying strength properties. It is highly sigm'ficant that for the solution heat treatment at 870, the potential measurement spread was over a range of 93 mv. For the other solution heat treatment temperature, 970 F., the spread was a little less at 74 mv. but still is considered excessively high. Similar results were encountered with the Composition B specimens as is seen in Table IV. Turning now to Table V and the Composition C results, it can again be seen that some variation in strength is caused by differing thermal treatments. However, it is readily apparent that the potential measurements did not vary appreciably. On the contrary, they were very stable. At a solution heat treatment of 870 F., the total potential spread amounted to only 10 mv. regardless of the precipitation hardening treatment. Equally significant, the results for solution heat treatment temperature of 970 F. indicate a total variation of only 13 mv. The total variation of all the results for Composition C amounts to only 29 mv. whereas for Compositions A and B, the total variation amounts to over 3 times that much, i.e., respectively, 93 and 96 mv. Where it is deemed essential for cathodic protection that TABLE II [Solution heat treatment and precipitation hardening conditions] Sol. H.T., hr. at F. Prec. hdn., hr. at F.
15.-.. do 24 at 340: 16--.- do 3 at 250 plus 3 at 325". 17 do a at 250 plus 15 at 325.
TABLE 111 [Strength and potential for Comp. A (0.08 81)] T.S. Y.S. Elong. Pot. S read (K s.i.) (K s.i.) (percent) (mv.) mv.)
Condition No.:
TABLE-IV [Strength and potential for Comp. B (0.46 Si) T.S. Y.S. Elong. Pot. Spread (K s.i.) (K s.i.) (percent) (mv.) (mv.)
Condition Na:
TABLE V [Strength and potential for Comp. C (0.76 Si) 'I.S. Y.S. Elong. Pot. Spread (K s.i.) (K s.i.) (percent) (mv.) (mv.)
Condition No.:
the anode potential be 100 mv. more anodic than the material being protected, this potential diiference being a common value often chosen in the industry, it can be seen that variations of 93 to 96 mv. can render positive assurance of this difference quite difiicult. It is apparent that the comparatively minuscule potential variation associated with the practice of the invention minimizes this problem.
Referring again to the tables, particularly Table V, it is apparent that the improved material exhibits substantial strength especially when solution heat treated at a temperature of over 950 F. In such cases, the tensile strength is over 45 K.s.i. regardless of the thermal treatment. Composite laminates, which included the improved anodic material as cladding, exhibited substantially higher strength than similar laminates featuring a non-heat treatable cladding and this strength improvement is realized without substantial variations in the solution potential of the cladding in response to varying thermal treatments thus rendering the improved material very useful as an anodic cladding layer.
What is claimed is:
1. An aluminum anode composed of a solution heat treatable and precipitation hardenable aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and a maximum of 0.25% copper and a maximum of 0.25% chromium, as impurities, said alloy article exhibiting, when subjected to a thermal exposure, a stable solution potential such that it does not vary by more than 50 mv. irrespective of the conditions of the thermal exposure.
2. The article according to claim 1 wherein the alloy also contains 0.1 to 0.75% manganese.
3. The article according to claim 1 wherein the silicon content amounts to l to 2 times the magnesium content.
4. The article according to claim 1 wherein the zinc content is 3.5 to 8%.
5. An article comprising a clad composite having a core and a cladding, said cladding being anodic to said core thereby to cathodically protect the core, said core and cladding each being composed of a heat treatable and precipitation hardenable aluminum base alloy, said cladding being composed of an aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and impurities with a maximum of 0.25 copper and a maximum of 0.25 chromium as impurities, said core being composed of an aluminum base alloy consisting essentially of 3 to 9% zinc, 0.5 to 3% magnesium, and copper present in an amount of up to 3%, the balance being aluminum and incidental elements and impurities, said core and cladding being adapted to common solution heat treatment and precipitation hardening treatments, said core exhibiting, after said treatments, a solution potential of from about 780 to about 850 mv. and said cladding exhibiting, after said treatments, a stable solution potential which does not vary by more than 50 mv. irrespective of the particular time and temperature employed in said treatments.
6. An article comprising a clad composite having a core and a cladding, said cladding being anodic to said core thereby to cathodically protect the core, said core and cladding each being composed of a heat treatable and precipitation hardenable aluminum base alloys, said cladding being composed of an aluminum base alloy consisting essentially of 2 to 8% zinc, 0.5 to 2% magnesium, 0.3 to 2% silicon, the silicon content amounting to at least 0.45 times the magnesium content, the balance being aluminum and incidental elements and impurities with a maximum of 0.25% copper and a maximum of 0.25% chromium as impurities, said core and cladding being adapted to common solution heat treatment and precipitation hardening treatments, said core exhibiting, after said treatments, a solution potential of from about 780 to about 850 mv. and said cladding exhibiting, after said treatments, a stable solution potential which does not vary by more than 50 mv. irrespective of the particular time and temperature employed in said treatments.
7. The article according to claim 5 wherein the cladding alloy additionally contains 0.1 to 0.75% manganese.
8. The article according to claim 5 wherein the cladding alloy silicon content amounts to 1 to 2 times its magnesium content.
7 8 9. The article according to claim 5 wherein the zinc OTHER REFERENCES Went the claddmg aHOY Metal Selector, 1953 ed., Steel, Oct. 14, 1963, pp.
References Cited UNITED STATES PATENTS 2,742,688 4/1956 Nock, Jr. 29-1975 5 L. DEWAYNE RUTLEDGE, Primary Examiner J. M. DAVIS, Assistant Examiner 3,287,185 11/1966 Nachet et a1. 75-141 X US. Cl. X.R. 3,342,565 9/ 1967 Munday et a1. 29-197.5 X 75146, 147
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US4560625A (en) * 1983-02-14 1985-12-24 Kabushiki Kaisha Kobe Seiko Sho Aluminum alloy composite materials for brazed heat exchangers
US4571368A (en) * 1983-01-17 1986-02-18 Atlantic Richfield Company Aluminum and zinc sacrificial alloy
US20060174980A1 (en) * 2004-10-05 2006-08-10 Corus Aluminium Walzprodukte Gmbh High-strength, high toughness Al-Zn alloy product and method for producing such product
US20070151636A1 (en) * 2005-07-21 2007-07-05 Corus Aluminium Walzprodukte Gmbh Wrought aluminium AA7000-series alloy product and method of producing said product
US20070204937A1 (en) * 2005-07-21 2007-09-06 Aleris Koblenz Aluminum Gmbh Wrought aluminium aa7000-series alloy product and method of producing said product
WO2008003504A3 (en) * 2006-07-07 2008-02-21 Aleris Aluminum Koblenz Gmbh Aa7000-series aluminium alloy products and a method of manufacturing thereof
US20080173378A1 (en) * 2006-07-07 2008-07-24 Aleris Aluminum Koblenz Gmbh Aa7000-series aluminum alloy products and a method of manufacturing thereof
US20090269608A1 (en) * 2003-04-10 2009-10-29 Aleris Aluminum Koblenz Gmbh Al-Zn-Mg-Cu ALLOY WITH IMPROVED DAMAGE TOLERANCE-STRENGTH COMBINATION PROPERTIES
US20090320969A1 (en) * 2003-04-10 2009-12-31 Aleris Aluminum Koblenz Gmbh HIGH STENGTH Al-Zn ALLOY AND METHOD FOR PRODUCING SUCH AN ALLOY PRODUCT

Cited By (16)

* Cited by examiner, † Cited by third party
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US4571368A (en) * 1983-01-17 1986-02-18 Atlantic Richfield Company Aluminum and zinc sacrificial alloy
US4560625A (en) * 1983-02-14 1985-12-24 Kabushiki Kaisha Kobe Seiko Sho Aluminum alloy composite materials for brazed heat exchangers
US20090269608A1 (en) * 2003-04-10 2009-10-29 Aleris Aluminum Koblenz Gmbh Al-Zn-Mg-Cu ALLOY WITH IMPROVED DAMAGE TOLERANCE-STRENGTH COMBINATION PROPERTIES
US10472707B2 (en) 2003-04-10 2019-11-12 Aleris Rolled Products Germany Gmbh Al—Zn—Mg—Cu alloy with improved damage tolerance-strength combination properties
US20090320969A1 (en) * 2003-04-10 2009-12-31 Aleris Aluminum Koblenz Gmbh HIGH STENGTH Al-Zn ALLOY AND METHOD FOR PRODUCING SUCH AN ALLOY PRODUCT
US20060174980A1 (en) * 2004-10-05 2006-08-10 Corus Aluminium Walzprodukte Gmbh High-strength, high toughness Al-Zn alloy product and method for producing such product
US7883591B2 (en) 2004-10-05 2011-02-08 Aleris Aluminum Koblenz Gmbh High-strength, high toughness Al-Zn alloy product and method for producing such product
US20070151636A1 (en) * 2005-07-21 2007-07-05 Corus Aluminium Walzprodukte Gmbh Wrought aluminium AA7000-series alloy product and method of producing said product
US20070204937A1 (en) * 2005-07-21 2007-09-06 Aleris Koblenz Aluminum Gmbh Wrought aluminium aa7000-series alloy product and method of producing said product
US20080210349A1 (en) * 2006-07-07 2008-09-04 Aleris Aluminum Koblenz Gmbh Aa2000-series aluminum alloy products and a method of manufacturing thereof
US20080173378A1 (en) * 2006-07-07 2008-07-24 Aleris Aluminum Koblenz Gmbh Aa7000-series aluminum alloy products and a method of manufacturing thereof
US20080173377A1 (en) * 2006-07-07 2008-07-24 Aleris Aluminum Koblenz Gmbh Aa7000-series aluminum alloy products and a method of manufacturing thereof
US8002913B2 (en) 2006-07-07 2011-08-23 Aleris Aluminum Koblenz Gmbh AA7000-series aluminum alloy products and a method of manufacturing thereof
US8088234B2 (en) 2006-07-07 2012-01-03 Aleris Aluminum Koblenz Gmbh AA2000-series aluminum alloy products and a method of manufacturing thereof
US8608876B2 (en) 2006-07-07 2013-12-17 Aleris Aluminum Koblenz Gmbh AA7000-series aluminum alloy products and a method of manufacturing thereof
WO2008003504A3 (en) * 2006-07-07 2008-02-21 Aleris Aluminum Koblenz Gmbh Aa7000-series aluminium alloy products and a method of manufacturing thereof

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