The present invention relates to an intermediate alloy for improving the performance of metals and alloys by refining grains, and, especially, to a grain refiner for magnesium and magnesium alloy and the method for producing the same.
The use of magnesium and magnesium alloy in industries started in 1930s. Since magnesium and magnesium alloys are the lightest structural metallic materials at present, and have the advantages of low density, high specific strength and stiffness, good damping shock absorption, heat conductivity, and electromagnetic shielding performance, excellent machinability, stable part size, easy recovery, and the like, magnesium and magnesium alloys, especially wrought magnesium alloys, possess extremely enormous utilization potential in the filed of transportation, engineering structural materials, and electronics. Wrought magnesium alloy refers to the magnesium alloy formed by plastic molding methods such as extruding, rolling, forging, and the like. However, due to the constraints in, for example, material preparation, processing techniques, anti-corrosion performance and cost, the use of magnesium alloy, especially wrought magnesium alloy, is far behind steel and aluminum alloys in terms of utilization amount, resulting in a tremendous difference between the developing potential and practical application thereof, which never occurs in any other metal materials.
The difference of magnesium from other commonly used metals such as iron, copper, and aluminum lies in that, its alloy exhibits closed-packed hexagonal crystal structure, has only 3 independent slip systems at room temperature, is poor in plastic wrought, and is significantly affected by grain sizes in terms of mechanical property. Magnesium alloy has relatively wide range of crystallization temperature, relatively low heat conductivity, relatively large volume contraction, serious tendency to grain growth coarsening, and defects of generating shrinkage porosity, heat cracking, and the like during setting. Since finer grain size facilitates reducing shrinkage porosity, decreasing the size of the second phase, and reducing defects in forging, the refining of magnesium alloy grains can shorten the diffusion distance required by the solid solution of short grain boundary phases, and in turn improves the efficiency of heat treatment. Additionally, finer grain size contributes to improving the anti-corrosion performance and machinability of the magnesium alloys. The application of grain refiner in refining magnesium alloy melts is an important means for improving the comprehensive performances and forming properties of magnesium alloys. The refining of grain size can not only improve the strength of magnesium alloys, but also the plasticity and toughness thereof, thereby enabling large-scale plastic processing and low-cost industrialization of magnesium alloy materials.
It was found in 1937 that the element that has significantly refining effect for pure magnesium grain size is Zr. Studies have shown that Zr can effectively inhibits the growth of magnesium alloy grains, so as to refine the grain size. Zr can be used in pure Mg, Mg—Zn-based alloys, and Mg-RE-based alloys, but can not be used in Mg—Al-based alloys and Mg—Mn-based alloys, since it has a very small solubility in liquid magnesium, that is, only 0.6 wt % Zr dissolved in liquid magnesium during peritectic reaction, and will be precipitated by forming stable compounds with Al and Mn. Mg—Al-based alloys are the most popular, commercially available magnesium alloys, but have the disadvantages of relatively coarse cast grains, and even coarse columnar crystals and fan-shaped crystals, resulting in difficulties in wrought processing of ingots, tendency to cracking, low finished product rate, poor mechanical property, and very low plastic wrought rate, which adversely affects the industrial production thereof. Therefore, the problem existed in refining magnesium alloy cast grains should be firstly addressed in order to achieve large-scale production. The methods for refining the grains of Mg—Al-based alloys mainly comprise overheating method, rare earth element addition method, and carbon inoculation method. The overheating method is effective to some extent; however, the melt is seriously oxidized. The rare earth element addition method has neither stable nor ideal effect. The carbon inoculation method has the advantages of broad source of raw materials and low operating temperature, and has become the main grain refining method for Mg—Al-based alloys. Conventional carbon inoculation methods add MgCO3, C2Cl6, or the like to a melt to form large amount of disperse Al4C3 mass points therein, which are good heterogeneous crystal nucleus for refining the grain size of magnesium alloys. However, such refiners are seldom adopted because their addition often causes the melt to be boiled. In summary, in contrast with the industry of aluminum alloys, a general-purpose grain intermediate alloy has not been found in the industry of magnesium alloy, and the applicable range of various grain refining methods depends on the alloys or the components thereof. Therefore, one of the keys to achieve the industrialization of magnesium alloys is to find a general-purpose grain refiner capable of effectively refining cast grains when solidifying magnesium and magnesium alloys.
The present invention provides an intermediate alloy for refining the grains of magnesium and magnesium alloys, which has great nucleation ability for magnesium and magnesium alloys. Also, the present invention provides a method for producing the intermediate alloy.
Surprisingly, the present inventor found that ZrC is a crystal nucleus having nucleation ability as many times as that of the Al4C3 in large number of studies on the refining of magnesium alloy grains, and the obtained Al—Zr—C intermediate alloy has relatively low melting point, so that it can form large amount of disperse ZrC and Al4C3 mass points, acting as the best non-homogeneous crystal nucleus for magnesium alloys.
The present invention adopts the following technical solutions: A grain refiner for magnesium and magnesium alloys, which is an aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy, having a chemical composition of: 0.01%˜10% Zr, 0.01%˜0.3% C, and Al in balance, based on weight percentage.
Preferably, the aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy has a chemical composition of: 0.1%˜10% Zr, 0.01%˜0.3% C, and Al in balance, based on weight percentage. The more preferable chemical composition is: 1%˜5% Zr, 0.1%˜0.3% C, and Al in balance.
Preferably, the contents of impurities present in the aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy are: Fe≤0.5%, Si≤0.3%, Cu≤0.2%, Cr≤0.2%, and other single impurity element≤0.2%, based on weight percentage.
A method for producing the grain refiner for magnesium and magnesium alloys according to the present invention comprises the steps of:
The present invention achieves the following technical effects: an intermediate alloy which has great nucleation ability and in turn excellent ability in refining the grains of magnesium and magnesium alloys is invented, which, as a grain refiner, is industrially applicable in the casting and rolling of magnesium and magnesium alloy profiles, enabling the wide use of magnesium in industries.
The present invention can be further clearly understood in combination with the particular examples given below, which, however, are not intended to limit the scope of the present invention.
968.5 kg commercially pure aluminum (Al), 30 kg zirconium (Zr) scrap and 1.5 kg graphite powder were weighed. The aluminum was added to an induction furnace, melt therein, and heated to a temperature of 1050° C.±10° C., in which the zirconium scrap and graphite powder were then added and dissolved. The resultant mixture was kept at the temperature under mechanical agitation for 100 minutes, and directly cast into Waffle ingots, i.e., aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy. Analysis was made under scanning electron microscope (SEM).
952.3 kg commercially pure aluminum (Al), 45 kg zirconium (Zr) scrap and 2.7 kg graphite powder were weighed. The aluminum was added to an induction furnace, melt therein, and heated to a temperature of 1200° C.±10° C., in which the zirconium scrap and graphite powder were then added and dissolved. The resultant mixture was kept at the temperature under mechanical agitation for 30 minutes, and directly cast into Waffle ingots, i.e., aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy.
989 kg commercially pure aluminum (Al), 10 kg zirconium (Zr) scrap and 1 kg graphite powder were weighed. The aluminum was added to an induction furnace, melt therein, and heated to a temperature of 1100° C.±10° C., in which the zirconium scrap and graphite powder were then added and dissolved. The resultant mixture was kept at the temperature under mechanical agitation for 45 minutes, and directly cast into Waffle ingots, i.e., aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy.
974 kg commercially pure aluminum (Al), 25 kg zirconium (Zr) scrap and 1 kg graphite powder were weighed. The aluminum was added to an induction furnace, melt therein, and heated to a temperature of 1300° C.±10° C., in which the zirconium scrap and graphite powder were then added and dissolved. The resultant mixture was kept at the temperature under mechanical agitation for 25 minutes, and directly cast into Waffle ingots, i.e., aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy.
900 kg commercially pure aluminum (Al), 97 kg zirconium (Zr) scrap and 3 kg graphite powder were weighed. The aluminum was added to an induction furnace, melt therein, and heated to a temperature of 1270° C.±10° C., in which the zirconium scrap and graphite powder were then added and dissolved. The resultant mixture was kept at the temperature under mechanical agitation for 80 minutes, and directly cast into Waffle ingots, i.e., aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy.
998.7 kg commercially pure aluminum (Al), 1 kg zirconium (Zr) scrap and 0.3 kg graphite powder were weighed. The aluminum was added to an induction furnace, melt therein, and heated to a temperature of 1270° C.±10° C., in which the zirconium scrap and graphite powder were then added and dissolved. The resultant mixture was kept at the temperature under mechanical agitation for 120 minutes, and directly cast into Waffle ingots, i.e., aluminum-zirconium-carbon (Al—Zr—C) intermediate alloy.
Mg-5% Al alloy was melt in an induction furnace under the protection of a mixture gas of SF6 and CO2, and heated to a temperature of 740° C., to which 1% Al—Zr—C intermediate alloy prepared according to example 1 was added to perform grain refining. The resultant mixture was kept at the temperature under mechanical agitation for 30 minutes, and directly cast into ingots.
The Mg-5% Al alloy before and after grain refining were analyzed and compared under scanning electron microscope.
Number | Date | Country | Kind |
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2011 1 0060735 | Mar 2011 | CN | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/CN2011/073182 | 4/22/2011 | WO | 00 | 6/22/2011 |
Publishing Document | Publishing Date | Country | Kind |
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WO2012/027990 | 3/8/2012 | WO | A |
Number | Name | Date | Kind |
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4612073 | Guzowski et al. | Sep 1986 | A |
Number | Date | Country | |
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20120039745 A1 | Feb 2012 | US |