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Overview
General information about Aluminium Alloying and strengthening of Al alloys Classification of Al alloys Wrought alloys (HT and non-HT) Cast alloys (HT and non-HT) Surface degradation of Al alloys
Aluminium
Soft, durable, lightweight, malleable metal Appearance range from silvery to dull gray, depending on the surface roughness. Most abundant metal in the Earth's crust, and the third most abundant element therein, after oxygen and silicon. The main source of aluminum is bauxite ore.
Bauxite ore
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Face-centered cubic (FCC) structure (a=0.40494 nm). nontoxic, nonmagnetic non-sparking Low melting temperature (660 C) Yield strength of pure aluminum is 711 MPa Yield strengths of Aluminium alloys can be up to 600 MPa. Aluminum has about one-third the density (2.70 g/cm3) and stiffness of steel (70GPa).
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Aluminium Alloys
Among the most striking characteristics of aluminum is its versatility. The range of physical and mechanical properties that can be developed from refined high-purity aluminum to the most complex alloys is remarkable. Principal interests in the physical metallurgy of aluminum alloys include the effects of composition, mechanical working, and/or heat treatment on mechanical and physical properties. Strength improvement is a major objective in the design of aluminum alloys because the low strength of pure aluminum (~10 MPa YS in the annealed condition) limits its commercial usefulness.
Physical Metallurgy
The elements that are most commonly present in commercial aluminum alloys to provide increased strength, particularly when coupled with strain hardening by cold working or with heat treatment, or both are copper, magnesium, manganese, silicon, and zinc. These elements all have significant solid solubility in aluminum, and in all cases the solubility increases with increasing temperature
Equilibrium binary solid solubility as a function of temperature for alloying elements most 6 frequently added to aluminum
Element Cu Cr Fe Li Mg Mn Ni Si
Temperature , C Maximum solid solubility, at% 548 661 655 600 450 658 640 577 2.4 0.4 0.025 16.3 18.5 0.9 0.02 1.59
Ag
Sn Ti Zn Zr
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228 665 443 661
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0.01 0.74 28.8 0.08
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Strengthening mechanisms
The predominant objective in the design of aluminum alloys is to increase strength, hardness, and resistance to wear, creep or fatigue. Different strengthening mechanisms are involved with different types of aluminum alloys. At elevated temperatures strength is improved mainly by solid-solution and second-phase hardening because for temperatures exceeding those of the precipitationhardening range, 230 C and over, the precipitation reactions continue into the softening regime. Strengthening in non-heat-treatable alloys occurs by solidsolution, second-phase constituents, and/or strain hardening. Heat treatable alloys are also strengthened by age/precipitation hardening.
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Solid-Solution Strengthening
The strength of high-purity annealed aluminum may be increased by solid solution hardening. For this to be achieved, the solute must: (1) have appreciable solid solubility at the annealing temperature; (2) remain in solution after a slow cool; and (3) not be removed by reacting with other elements to form insoluble phases. For those elements that form solid solution, the strengthening effect when the element is in solution tends to increase with increasing difference in the atomic radii of the solvent (Al) and solute (alloying element) atoms. Of the commonly used elements, only zinc, magnesium, copper and silicon have significant solubilities
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Precipitation hardening
Heat treatment for precipitation strengthening involves: 1) Solution heat treatment at a high temperature to maximize solubility 2) Rapid cooling or quenching to a low temperature to obtain a solid solution supersaturated with both solute elements and vacancies
(Solution heat treatments are designed to maximize the solubility of elements that participate in subsequent aging treatments. They are most effective near the solidus or eutectic temperature, where maximum solubility exists and diffusion rates are rapid. However, care must be taken to avoid incipient melting of low-temperature, eutectics and grainboundary phases. Such melting results in quench cracks and loss in ductility. The maximum temperature may also be set with regard to grain growth, surface effects, and economy of operation. The minimum temperature should be above the solvus, or the desired properties derived from aging will not be realized.)
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3) Aging treatments
The high strength is produced by the finely dispersed precipitates that form during aging heat treatments. This final step must be accomplished not only below the equilibrium solvus temperature, but below a metastable miscibility gap called the Guinier-Preston (GP) zone solvus line. The supersaturation of vacancies allows diffusion, and thus zone formation, to occur much faster than expected from equilibrium diffusion coefficients. In the precipitation process, the saturated solid solution first develops solute clusters, which then become involved in the formation of transitional (non-equilibrium) precipitates. The final structure consists of equilibrium precipitates, which do not contribute to age hardening (precipitation strengthening).
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GP zones
Intermediate stage 2
Intermediate stage 3
Equilibrium phase
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Precipitation heat treatment or artificial aging curves for the Al-Mg-Si wrought alloy 6061 (which is widely used for structural shapes) are shown below. This is a typical family of curves showing the changes in tensile yield strength that accrue with increasing time at each of a series of temperatures.
Precipitation heat treatment or artificial aging curves for solution heat-treated aluminum alloy 6061
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Classification of Al alloys
Aluminum alloys generally can be divided into two major categories: Casting alloys and Wrought alloys. A further differentiation for each category is based on the primary mechanism of property development. Many alloys respond to thermal treatment based on phase solubilities. These treatments include solution heat treatment, quenching, and precipitation, or age hardening. For either casting or wrought alloys, such alloys are described as heat treatable alloys. A large number of other wrought compositions rely instead on work hardening through mechanical reduction, usually in combination with various annealing procedures for property development. These alloys are referred to as non-heat treatable alloys. Some casting alloys are essentially not heat treatable and are used only in as-cast or in thermally modified conditions unrelated to solution or precipitation effects.
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Flat rolled products (sheet, plate and foil) Rod, bar and wire Tubular products Shapes Forgings
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Typical applications include beverage cans, cooking utensils, heat exchangers, storage tanks, furniture, highway signs, roofing and other architectural applications.
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Certain limitations are placed on the amount of cold work and the safe operating temperatures permissible for the higher-magnesium alloys (over about 3.5% for operating temperatures above about 65C) to avoid susceptibility to intergranular attach stress-corrosion cracking. It is because there is a tendency for the -phase, Mg5Al8, to precipitate in slip bands and grain boundaries. The other problem is that work-hardened alloys may undergo what is known as age softening at ambient temperatures. Over a period of time, the tensile properties fall due to localized recovery within the deformed grains.
Al-Mg alloys are widely used for welded applications. In transportation, structural plate is used for dump truck bodies, large tanks for carrying petrol, milk and grain, and pressure vessels, particularly where cryogenic storage is involved. Their high corrosion resistance makes them suitable for the hulls of small boats and for the super structures of ocean-going vessels. In addition, they polish to a bright surface finish, particularly if made from high quality aluminum, and are used for automotive trim and architectural components.
Number EC 1xxx
3xxx
5xxx
Manganese
Magnesium
3003 (1.2%Mn)
5052 (2.5%Mg, 0.25%Cr)
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Alloy 2024 Fuselage and lower wing due to its good fatigue resistance and fracture toughness
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7150 or 7449 or 7075 for upper wing skin due to good fatigue resistance, fracture toughness and compressive strength
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Number 2xxx
Examples 2014 (4.5%Cu, 0.5%Mg; 0.8%Mn; 0.8%Si) 2024 (4.5%Cu, 1.5%Mg, 0.6%Mn) 6061 ((1%Mg, 0.6S%Si, 0.3%Cu) 6063 (0.7%Mg, 0.4%Si
6xxx
Mg + Si
7xxx
Zn
7075 (5.6%Zn, 1.6%Cu, Aircraft 2.5%Mg) Wrought heat treatable Aluminium alloys
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1. 2. 3. 4. 5. 6. 7.
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380 390
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In hypereutectic Al-Si alloys, refinement of the proeutectic silicon phase by phosphorus additions is essential for casting and product performance.
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Aluminum-silicon phase diagram and cast microstructures of hypoeutectic compositions (<12%Si), hypereutectic compositions (>12% Si), and one close to the eutectic composition of 12% Si
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Aluminum - Magnesium Casting Alloys (5xx.0) Aluminum-magnesium casting alloys are essentially single-phase binary alloys with moderate-to-high strength and toughness properties. High corrosion resistance, especially to seawater and marine atmospheres, is the primary advantage of castings made of Al-Mg alloys. Best corrosion resistance requires low impurity content (both solid and gaseous), and thus alloys must be prepared from high-quality metals and handled with great care in the foundry. These alloys are suitable for welded assemblies and are often used in architectural and other decorative or building needs. Aluminummagnesium alloys also have good machinability and an attractive appearance when anodized. In comparison to the aluminum-silicon alloys, all the aluminummagnesium alloys require more care in gating and greater temperature gradients to produce sound castings. This often means more chilling and larger risers. Also, careful melting and pouring practices are needed to compensate for the greater oxidizing tendency of these alloys when molten. Care is also needed because many of the applications of these alloys require polishing and/or fine surface finishing, where defects caused by oxide inclusions are particularly undesirable. The relatively poor castability of Al-Mg alloys and the tendency of the magnesium to oxidized increase handling difficulties, and therefore, cost.
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Discontinuous silicon carbide/aluminum castings. Pictured are a sand cast automotive disk brake rotor and upper control arm, a permanent mold cast piston, a high-pressure die cast bicycle sprocket, an investment cast aircraft hydraulic manifold, and three investment cast engine cylinder inserts. Courtesy of Dural Aluminum Composites Corporation
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Corrosion
Aluminum is only less active than beryllium and magnesium among structural metals. Nevertheless, aluminum and its alloys are excellent corrosion resistant in most environments due to the rapid formation of a natural oxide film of alumina on the surface that inhibits the bulk reaction predicted from thermodynamic data. The oxide film developed in air is very thin (about several nm). It may continue to grow at a decreasing rate for several years to reach a thickness of some tens of nanometers. The rate of film growth becomes more rapid at higher temperature and higher relative humidity, so in water it is many times that occurring in dry air. In aqueous solutions, it has been suggested that the initial corrosion product is aluminium hydroxide, which changes with time to become a hydrated aluminum oxide. The main difference between this film and that formed in air is that it is less adherent and so is far less protective. As a general rule, the protective film is stable in aqueous solutions of the pH range 4.5-8.5, whereas it is soluble in strong acids or alkalis, leading to rapid attach of the aluminum.
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Wear behaviour
Aluminum alloys have been used for tribological applications since about 1940, when cast aluminum-tin bearings were introduced for heavy machinery. The development of aluminum-silicon alloys spurred even greater interest in lightweight aluminum alloys for wear-resistant components. The two major types of wear relevant to industrial applications of aluminum-silicon alloys are abrasive and sliding wear. Although the different aluminum-silicon alloys show the same wear mechanisms, the wear behavior is different due to the various microstructures. In the aluminum-silicon alloys, the hard silicon particles are surrounded by a softer and relatively tough matrix. With increasing the amount of silicon particles, higher overall levels of hardness can be obtained. This results in better wear resistance. To be noted, under relatively light load conditions, which are normally associated with low (<10-11 m3/m) losses, wear resistance is not a strong function of silicon content.
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The complex effects of composition on wear behavior suggest that wear resistance depends on other material properties (for example, fracture toughness). Thus lower fracture toughness at higher levels of silicon could lead to higher wear rates if larger pieces of debris are created during the wear process. Variations in toughness and strength with composition might also account for the apparent ability of the near-eutectic compositions to have a greater load-bearing capability at a given wear rate than either higher or lower silicon levels matrix hardness. Increased matrix hardness is typically achieved through the heat treatment response produced by copper and magnesium additions. Most commercial applications of aluminum-silicon alloys, in fact, depend on the increased strength achieved by heat treatment. The improved wear resistance of precipitation-strengthened material compared to solid solution strengthened material under low wear conditions was also noted using aluminum alloy 6061, which is strengthened primarily by Mg2Si precipitates. This is also the strengthening mechanism in the heattreatable magnesium-bearing aluminum-silicon alloys. Although heat treatment has a beneficial effect, variations in matrix hardness may be less important than the effects of silicon content.
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