Classifications

• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C18/00—Alloys based on zinc
  • C22C18/04—Alloys based on zinc with aluminium as the next major constituent

Definitions

• ABSTRACT A zinc-aluminum alloy consisting of 18 to 24% by weight (preferably 21% by weight) aluminum, the bal-- ance zinc and 0.1 to 1.5% by weight nickel (preferably 0.3 to 1.0% by weight).
• the nickel component represents a further metal for which can be substituted, to an amount of about 50% by weight, titanium in an amount of 0.05 to 0.5% by weight of the alloy, copper up to 0.5% by weight of the alloy, iron in an amount of up to 0.75% by weight of the alloy, and silicon in an amount of up to 0.75% by weight of the alloy.
• the lead, cadmium and tin content should be no greater than 0.05% by weight of the alloy and the magnesium content is preferably less than 0.0005% by weight of the alloy.
• ductile metals facilitating shaping in dies or the like.
• Typical shaping methods include extrusion, drawing and die-casting and, depending upon the requirements of the alloy, bodies composed thereof must be capable of withstanding bending, folding, compression and tensile stresses. It is advantageous, therefore, to have high ductility and resistance to rupture, high resistance to fatigue and high strength, e.g. compressive strength and tensile strength. It is also important that these characteristics be present at room temperature, the bodies being most frequently used at this temperature or at a mean. temperature close to room temperature.
• binary zincaluminum alloys in which some of the ductile charac teristics of zinc and the compressive-strength characteristics of aluminum can be combined.
• binary zinc-aluminum alloys containing between I and 63 percent by weight aluminum and 99 to 37 percent by weight zinc. (the'balance) have been studied.
• the solid solution develops in a fine-grained eutectic crystalline structure and yields an alloy of high ductility which can be plastically deformed readily with relatively low mechanical stress.
• Such alloys are advantageous for die forming, extrusion and drawing.
• the alloy is amenable to vacuum-forming, i.e. foils of the metal, e.g. prepared by lowering, can be vacuum-formed in a manner analogous to the formation of blisters, bubbles, containers and the like from thermoplastic foils.
• this unique method of forming which was not generally possible earlier in the metal-working art, opens new vistas in the processing of sheet metals.
• Such zinc-aluminum alloys in this state, with compressive strength of 16 to 20 kg/mm have elongation values of more than 100 percent, so that bands, sheets and strips of the metal can be bent or folded through l80 without rupture or crack formation and can be used more effectively in deep-drawing.
• these highly ductile zinc-aluminum alloys have the disadvantage that the creep resistance of the metal is low.
• creep resistance it will'be understood that it is intended to designate the load which can be applied to the workpiece which will develop a shape change of more than 1 percent per year.
• the desired alloys under discussion have a creep resistance of, say, 0.4 kg/mm and this value is extremely low, even lower than that of unalloyed zinc.
• Another object of the invention is to provide a zincaluminum-based alloy having high tensile strength, a higher creep resistance than has been attainable heretofore with such alloys, and yet has an effective ductil- 1ty.
• high-ductility zinc/aluminum alloy which possesses high creep resistance
• the alloy consisting essentially of 18 to 24 percent by weight of aluminum, 0.1 to L5 percent by weight of a further metal component consisting in larger measure of nickel and the balance, i.e. 74.5 to 81.9 percent by weight highgrade zinc.
• high-grade zinc is used herein to refer to zinc in accordance with ASTM specification B6 49 and containing a maximum of 0.006 percent by weight lead, 0.005 percent by weight iron, 0.004 percent by weight cadmium and, generally, having a total impurity level no greater than 0.050 percent by weight.
• the high-grade zinc of the present invention is 99.95 percent pure.
• the third component i.e. the nickel-containing component, constitutes 0.3 percent by weight to l.0 percent by weight of the alloy while the aluminum content is preferably 21 percent by weight.
• the third metallic component of the alloy may consist entirely of nickel percent by weight of the third component which constitutes 0.1 to 1.5 percent by weight of the alloy), although it has been found desirable to add or provide other metals, preferably in lesser proportion than the nickel, as part of this third metallic component.
• the nickel content can, according to the invention, be replaced at least in part (up to 50 percent of the nickel or third metallic component) with 0.05 to 0.5 percent by weight titanium.
• the nickel and/or titanium component can be substituted with up to 0.5 percent by weight copper (0 to 5 percent) as long as the copper content does not exceed 50 percent of the nickel and/or titanium content.
• the nickel content of the alloy is 1 percent by weight and the titanium content is 0.5 percent by weight, neither copper nor any of the other possible constituents of the third metallic components can be present.
• the nickel content is 0.75 percent by weight, the titanium content can reach 0.375 percent by weight and a copper content of 0.375 percent by weight is permissible by virtue of the upper limit of the third metallic component (1.5 percent) of the alloy.
• the copper content will be at most 50'percent of the titanium content so that, in the present example, the upper limit of the copper content will be 0.188 percent.
• the alloy may contain, as part of the third component, iron and/or silicon in an amount ranging up to 50 percent by weight of the nickel and/or titanium content. In all cases, however, it' is important that the lead, cadmium and tin contents of the alloy be collectively less than 0.05 percent by weight and that the magnesium content be below 0.0005 percent.
• the alloying components incorporated in the zinc-aluminum matrix are insoluble in zinc and aluminum in the solid state and constitute, in the dendritic structure, intermediate phases in finely defined form, I provide a rapid cooling of the melt to ensure the maintenance of the fine-grained structure. According to an important feature of the present invention, therefore,
• the volume of the metal body (extruded) should be 5 to mm", preferably 8 to 15 mm.
• the extruded body, billet or bar may have a rollable thickness of 10 to 50 mm, preferably 16 to mm.
• the rapid cooling and solidification results in rapid crystal formation so that it is advisable, according to the invention, to permit equilibration or homogenization of the lattice structure for a relatively long period at a temperature of 300 to 380C. 1 have found that such a procedure yields an increase in the creep resistance of the metal body of five to eight times as compared with conventional alloys.
• the alloy of the present invention is malleable and can be employed for the production of plates, strips, bands, tubes and bars of various configurations in the manner currently employed with the production of extruded articles.
• Example 1 representing the system of the present invention
• Example 11 representing a control in which features of the invention are omitted for the purpose of comparison.
• EXAMPLE I An alloy is prepared by melting high-purity zinc, aluminum and nickel to yield a composition of 78 percent by weight zinc, 21 percent by weight aluminum and 1 percent by weight nickel.
• the extruded block is provided with 1 mm of cooling surface for each 10 mm of volume and is rolled to a square cross-section, 4 cm on each side.
• Example 2 Upon solidification of the block to a temperature of 220C over a period of 10 seconds, the elongation to break was 125 percent and the creep resistance was 1.2 kg/mm A block of the same dimension cooled to room temperature over a solidification and cooling time of 2 seconds had an elongation to break of 120 percent and a creep resistance of 2.8 kg/mm EXAMPLE II A zinc-aluminum alloy containing 79 percent by weight zinc and 21 percent aluminum was produced and treated in the manner described in Example 1.
• creep resistance was found to range between I and 3 kg/mm, or 2.5 to six times that of a composition omitting the third component, while the elongation to break or ductility was equal to that of the composition without the third component or deviated therefrom by less than 10 percent;
• the alloy in each case, was extruded at a temperature close to the melting point in a bar having a thickness of 20 mm and a circumference such that for each 10 mm of extruded volume, the surface area at which cooling was effected was 1 mm
• the bar was rapidly cooled to room temperature in a period of 2 seconds. Thereafter, the bar was brought to a temperature of 350C and maintained at this temperature for a period of minutes to 5 hours (preferably 30 to 60 minutes) for homogenization.
• a zinc-aluminum alloy consisting essentially of a first metallic component consisting of aluminum in an amount between 18 and 24 percent by weight of the alloy, a second metallic component consisting of zinc in amount of copper being up to 0.5 percent by weight of the alloy, and the total amount of copper, iron, and silicon in the alloy not exceeding 50 percent by weight of the total content of nickel and titanium in the alloy.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Mechanical Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Gates (AREA)
• Continuous Casting (AREA)
• Extrusion Of Metal (AREA)

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Cited By (6)

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• 1969
  • 1969-07-09 DE DE19691934788 patent/DE1934788A1/de active Pending
• 1970
  • 1970-06-24 FR FR7023353A patent/FR2056326A5/fr not_active Expired
  • 1970-06-24 BE BE752448D patent/BE752448A/xx unknown
  • 1970-06-24 GB GB1257445D patent/GB1257445A/en not_active Expired
  • 1970-07-07 US US00053039A patent/US3785811A/en not_active Expired - Lifetime
  • 1970-07-08 NL NL7010110A patent/NL7010110A/xx unknown

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