AU2000276884B2

AU2000276884B2 - High strength magnesium alloy and its preparation method

Info

Publication number: AU2000276884B2
Application number: AU2000276884A
Authority: AU
Inventors: Soon Chan Park; Kwang Seon Shin
Original assignee: Individual
Current assignee: Individual
Priority date: 2000-09-26
Filing date: 2000-09-26
Publication date: 2005-09-29
Anticipated expiration: 2020-09-26
Also published as: CN1469937A; EP1339888A4; JP3891933B2; CA2423459A1; ATE505567T1; WO2002027053A1; DE60045848D1; JP2004510057A; NO20031349D0; EP1339888B1; AU7688400A; CA2423459C; EP1339888A1; IL154897A; IL154897A0; NO20031349L; CN100390313C

Abstract

The present invention provides high strength magnesium alloys consisting essentially of 3 SIMILAR 10 wt.% Zn, 0.25 SIMILAR 3.0 wt.% Mn, and the balance of Mg and inevitable impurities, the high strength magnesium alloy further containing 1 SIMILAR 6 wt.% Al, 0.1 SIMILAR 4.0 wt.% Si, and 0.1 SIMILAR 2.0 wt.% Ca, in order to provide a high strength magnesium alloy having an improved hardness and strength, and an excellent elongation at an ambient temperature. In addition, the present invention provides a method for preparing the high strength magnesium alloy characterized in that a Zn-Mn mother alloy is added to a magnesium melt by a fluxless melting method, and process conditions for working and heat-treating an obtained cast material.

Description

HIGH STRENGTH MAGNESIUM ALLOY AND ITS PREPARATION METHOD Field of the invention The present invention relates to high strength magnesium alloys and a method for preparing the same, and more specifically to magnesium alloys having 00 00 improved mechanical properties including strength, hardness, and elongation while having an improved formability, high strength and elongation and their (-i Seconomical processing method, by adding specific alloying elements or changing Sprocessing conditions including specific heat treatments.

Background of the invention In this specification, where a document, act or item of knowledge is referred to or discussed, this reference or discussion is not an admission that the document, act or item of knowledge or any combination thereof was at the priority date: part of common general knowledge; or (ii) known to be relevant to an attempt to solve any problem with which this specification is concerned.

Among magnesium alloys, Mg-Zn-based alloys exhibit a superior age hardening behavior. These alloys exhibit relatively high strength and ductility while having advantages in that it is easilyprocessible and weldable. On the other hand, Mg-Zn-based alloys have also disadvantages since it is difficult for them to be applied to a casting process such as die-casting because the addition of Zn to Mg tends to increase the formation of micropores during casting.

Furthermore, such Mg-Zn-based alloys have a limitation in improvement in Strength because it is not easy to refine the microstructure by the addition of alloying elements or an over-heating heat treatment, compared to other magnesium alloys. This limitation has restricted their commercial applications.

tvlm M01 1673545v3 305162074 WO 02/27053 PCT/KR00/01072 In order to solve these problems, research efforts have been made to add alloying elements to an Mg-Zn binary alloy. Examples of these research efforts are as follows.

In 1947, J. P. Doan and G. Ansel have proposed a method in which Zr is added to an Mg-Zn-based alloy to refine the grain size of the alloy, thereby improving the strength of the alloy P. Doan and G. Ansel, Trans.

AIME, vol. 171 (1947), pp. 286-295). In this method, however, there is a difficulty in adding Zr to magnesium melts because Zr has a high melting point.

Also, the addition of rare earth elements such as La, Ce or Nd, or Th to Mg-Zn alloy has been known. This method is known to have advantages in that it is possible to reduce micro-pore formation and improve strength at high temperatures and weldability. However, this method has significant cost disadvantages due to expensive alloying elements, compared to other magnesium alloys.

In 1987, W. Unsworth and J. F. King have reported that the ductility of Mg-Zn alloys might be improved by refining the P1' phase, which is the major strengthening precipitation phase of Mg-Zn alloy, by the addition of Cu to the Mg-Zn alloy Unsworth and J. F. King, Magnesium Technology, The Inst. of Metal, 1987, pp. 25-35). However, the addition of Zn and Cu involves a limited elongation of less than 10 at ambient temperature even though the elongation may be slightly increased depending upon the added amounts of those elements.

The following Table 1 shows tensile properties of commercial cast alloys and wrought alloys.

WO 02/27053 WO 02/7(153PCTKROOO 1072 Table 1 Properties of Commercial Magnesium Alloys Composition ()Tensile Properties Tensi Yield le Stren Stren Elonga T Z gth gth tion Alloys Al Mn h Zn r Others (MPa) (Mpa) N% Cast AZ91 C- 8.7 0.13 -0.7 145 275 6 EQ2IA- 0. 1.5 Ag, 195 235 2 HK31A- 3. 0. 105 220 8 WE54A- 0. 5.2 Y, 172 250 2 ZC63A- 0.25- 6.0 2.7 Cu 125 210 4 ZE63A- 5.8 0. 2.6 RE 190 300 ZK61A- 6.0 0. 195 310 Die-cast 6.0 0.13 115 205 6 AS41A-F 4.3 0.35 1.0 Si 150 220 4 AZ91A,B 9.0 0.13 0.7 150 230 3 Extrude AZ8OA- 8.5 0.5 275 380 7 M1IA-F 1.2 180 255 12 ZC71 -F 0.5-1.0 6.5 1.2 Cu 340 360 HM31A- 1.2 3. 230 290 ZK6OA- 5.5 0. 305 365 11 Sheet AZ31IB- 3.0 1.0 220 290 HK31A- 3. 0. 200 255 9 HM2IA- 0.6 2. 170 235 11 PE 3.3 0.7 Referring to Table 1 it can be found that commercial wrought alloys generally exhibit higher yield strength, tensile strength, and elongation compared to commercial cast alloys. Even in the case of commercial wrought alloys. However, it is difficult even for the existing commercial wrought alloys to obtain a combination of high strength and high elongation. That is, high strength alloys exhibiting a high tensile strength exceeding 300 MPa have a drawback in that their elongation rarely exceeds about 10%. It has also been reported that, in the case of Zn and Zr-added alloys exhibiting superior properties 00 in terms of strength, there are many restrictions on preparing processes in adding 00 O Zr.

US Patent No. 4,997,622 discloses properties of magnesium alloys prepared by a rapid solidification processing method. According to this Patent, magnesium (Ni alloys prepared by a rapid solidification processing method exhibit improved yield strength, tensile strength and elongation. However, the results of research made up to the present show that those alloys have high processing costs and limited applications, compared to the existing commercial alloys.

DISCLOSURE OF THE INVENTION One embodiment of the invention provides high strength magnesium alloys exhibiting improvements in refining of the microstructure and precipitation behavior, enhancements in mechanical properties such as hardness, strength, and elongation, and an improvement in formability in accordance with an addition of alloying elements, less expensive than those conventionally used, to an Mg-Znbased alloy.

A further embodiment of the invention provides a method for preparing high strength magnesium alloys exhibiting a definitely superior elongation, compared to strength, using an optimum heat treatment condition, and to provide an economical processing condition for the preparation method.

In accordance with one aspect, the present invention provides high strength magnesium alloys consisting of 3 10 wt. Zn forming a precipitation phase in the alloy, 0.25 3.0 wt. Mn present in the form ofa-Mn in the alloy and refining the precipitation phase, and the balance of Mg and impurities.

The magnesium alloy may further comprise 1 6 wt.% Al. Also, the magnesium alloy may further contain 0.1 4.0 wt. Si, or a combination of 0.1tvlm MOl 11673545v4 305162074

I

c 4.0 wt. Si and 0.1 2.0 wt. Ca. Preferably, the content of Al is not more than the content of Zn.

Preferably, the content of Zn is 5.0 7.0 wt. the content of Mn is 0.75 O 2.0 wt. the content of Si is 1.5 3.0 wt. %,'and the content of Ca is 0.3 1. 0 wt.%.

00 O An important feature according to a preferred embodiment of the present invention is to add Al, as an alloying element, to an Mg-Zn-based alloy so as to Cachieve a decrease in yield strength resulting in an improvement in formability and an enhancement in work hardening ability, thereby to provide a high strength magnesium alloy having a high strength and a high elongation.

In accordance with another aspect, the present invention provides a method for preparing the high strength magnesium alloy, in which an addition of Mn to a magnesium melt is achieved by adding a Zn-Mn mother alloy to the magnesium melt.

Preferably, the high strength magnesium alloy is prepared in the form of a cast ingot by adding a Zn-Mn mother alloy having an Mn content of 10 20 wt. 20 wt. Mn mother alloy) to the magnesium melt in a temperature range of 670 to 720°C, and adding Zn or Zn along with Al to the magnesium melt.

Alternatively, the high strength magnesium alloy may be preferably prepared in the form of a cast ingot by adding a Zn-10-20 wt. Mn mother alloy to the magnesium melt in a temperature range of 670 to 720°C, adding an Mg-Si mother alloy to the magnesium melt, and adding Zn or Zn along with Al and/or Ca to the magnesium melt.

Preferably, the cast ingot may be subsequently subjected to a homogenization process in a temperature range of 340 to 410°C for 6 to 12 hours, so that it is formed into a billet. The billet may be mechanically worked after being preheated in a temperature range of 150 to 400C for 30 minutes to 2 hours.

More preferably, the worked or wrought body may be subjected to a primary aging process in a temperature range of 70 to 100°C for 24 to 96 hours, and then to a secondary aging process in a temperature range of 150 to 180'C for 48 hours or more.

tvlm MO 111673545v3 305162074 Prior to the double aging process, a solution heat treatment may be carried out in a temperature range of 340 to 410 0 C for 6 to 12 hours. Alternatively, a stretching of 3 to 7% may be carried out prior to the double aging process.

The reason why the composition range of each alloying element used in accordance with the present invention is limited to the above mentioned range is as follows Zinc (Zn):3 10 wt. The maximum solid solubility limit of Zn in an Mg matrix is 6.2 wt. at 340 0 C. Where Zn is added in an amount of 3.0 wt. or more to Mg matrix, it forms an acicular precipitation phase when it is subjected to a heat tvlm MO111673545v3 305162074 WO 02/27053 PCT/KR00/01072 treatment, thereby exhibiting an age hardening behavior. Generally, the content of Zn is determined, based on the solid solubility limit thereof. When Zn is added in an amount of about 5.0 7.0 wt.% approximating to the maximum solid solubility limit thereof, it is possible to obtain a maximized age hardening behavior. At the Zn content of not more than 3.0 wt.% corresponding to a minimum solid solubility limit at a general aging temperature, it is difficult to expect a desired precipitation strengthening phenomenon because of an insufficient formation of precipitation phase. On the other hand, when Zn is added in an amount of 10.0 wt.% or more, precipitation of equilibrium phases at grain boundaries is promoted. As a result, degradation in mechanical properties may occur. Accordingly, the content of Zn is limited to a range of 3 10 preferably a range of 5.0 in accordance with the present invention.

Manganese 0.25 3.0 wt.% The maximum solid solubility limit of Mn in an Mg matrix is about 2.2 wt.% at 650 0 C corresponding to the melting point of Mg. The solid solubility limit of Mn is rapidly decreased at lower temperatures, so that Mn may be present in the form of a-Mn in the Mg matrix. It is generally known that, in magnesium alloys, Mn contributes to an improvement in corrosion resistance when it is added in an amount of 0.1 wt.% or more. Where Mg is added for purposes other than the improvement in corrosion resistance, for example, a strengthening purpose, it may contribute to an improvement in the strength of the alloy product at its content of 0.25 2.0 wt.% even though the effect may be varied, depending on the matrix alloy of the alloy product. In WO 02/27053 PCT/KR00/01072 particular, the inventors experimentally found that Mn existing in the wrought body serves to refine the precipitation phase of the Mg-Zn binary alloy when the wrought body is subjected to an aging process following a solution heat treatment, thereby providing effects of an improvement in strength and an improvement in elongation. Based on this fact, addition of Mn is made to strengthen the alloy in accordance with the present invention. In this regard, the minimum content of Mn is determined to be 0.25 wt.% in accordance with the present invention. Taking into consideration the maximum solid solubility limit of Mn and the processing method used, it is difficult to add a large amount of Mn using a general melting process. Where Mn is added in an amount of 3.0 wt.% or more, it is mainly present in the form of a-Mn in the matrix. Thus, the surplus amount of Mn does not contribute to the improvement in the properties of the alloy, but results in an undesirable result in terms of the preparation costs. Accordingly, the content of Mn is limited to a range of 0.25 3.0 preferably a range of 0.75 2.0 wt.%, in accordance with the present invention.

Aluminum 1 6 wt.% In an Mg matrix, Al exhibits a maximum solid solubility limit of about 12 wt.% at 4370C. It is known that an Mg 17

AI

12 precipitation phase is formed in Mg-AI binary alloys in accordance with a heat treatment used. However, addition of Al according to the present invention is irrespective of the formation of such Mg 17 A1 12 precipitation phase. In accordance with the present invention, the addition of Al is adapted to improve the major strengthening phase in an Mg-Zn-Mn-based ternary alloy, that is, the Mg-Zn- WO 02/27053 PCT/KR00/01072 based acicular precipitation phase. Accordingly, the content of Al is determined within a range involving limited formation of Mg-Al-based precipitation phases, taking into consideration the temperature range of heat treatment, such as the aging temperature range, and the content of Zn added as a major alloying element. The lower content limit of Al is determined to be 1.0 wt.% because the solid solubility limit of Al in the Mg matrix corresponds to about 1 wt.% in the aging temperature range. In order to limit the formation of an Mg-Al-based precipitation phase resulting from a surplus amount of Al exceeding the content of Zn, the upper content limit of Al is determined to be 6.0 Meanwhile, where Al is added in an amount considerably more than the added amount of Zn, the possibility of the formation of the Mg-Al-based precipitation phase, that is, the Mg 17 A1 12 precipitation phase, is greatly increased. Such a precipitation phase may be coarsely precipitated at grain boundaries, and even interior of grains at a certain heat treatment temperature. Since this precipitation phase is very brittle in terms of strength, it provides a fracture path when the alloy is subjected to a fracture, thereby resulting in a degradation in strength. For this reason, it is desirable for the content of Al to be less than the content of Zn. The inventors experimentally found that Al present in the wrought body exhibits effects of refining acicular precipitation phases even without a solution heat treatment for the wrought body, and providing a remarkable improvement in tensile strength and, in particular, elongation, even though there is a slight decrease in yield strength. It was also found that an increase in the content of Al results in a decrease in yield strength while causing an increase in tensile strength.

WO 02/27053 PCT/KR00/01072 Silicon 0.1 4.0 wt.% Because silicon is hardly soluble in an Mg matrix, Si forms an Mg 2 Si phase, when it is added to the Mg matrix as an alloying element. Such a compound may provide a dispersion strengthening effect when its morphology and/or size is modified in the preparation and heat treatment procedures of the wrought body. The inventors experimentally found that a desired dispersion strengthening effect, as mentioned above, is obtained when Si is added to an Mg-Zn-Al-Mn-based quaternary alloy. When the content of Si is less than 0.1 the intended effect of the Si addition can hardly be expected. At an Si content of more than 4.0 coarse Mg 2 Si is formed, thereby resulting in a decrease in elongation. In this regard, the content of Si is limited to a range of 0.1 4.0 preferably a range of 3.0 in accordance with the present invention.

Calcium 0.1 2.0 wt.% In the case of an Mg alloy containing Si, it is possible to reduce the grain size of the alloy while improving the morphology of the Mg 2 Si phase, in accordance with an addition of Ca. To this end, Ca is added to an Sicontaining Mg-Zn-Al-Mn alloy in accordance with the present invention. At a Ca content of less than 0.1 it is hardly expected to observe the effect of improving the Mg 2 Si phase. On the other hand, when Ca is added in an amount of 2.0 wt.% exceeding considerably the maximum solid solubility limit of Ca in the Mg matrix at 516 0 C, that is, 1.34 an Mg 2 Ca precipitation phase is formed. Due to such an Mg 2 Ca precipitation phase at WO 02/27053 PCT/KR00/01072 grain boundaries, beside the effect of improving the Mg 2 Si phase, there is a degredation in strength. The inventors experimentally found that it is possible to more effectively control the morphology of the Mg 2 Si phase formed in the Mg-Zn-Al-Mn alloy at a Ca content of 0.3 1.0 and thus to obtain improvements in strength and elongation. In this regard, the content of Ca is limited to a range of 0.1 2.0 and preferably 0.3 1.0 in accordance with the present invention.

In addition, the principal impurities of the Mg alloy should be appropriately limited because they mainly have fatally adverse affects on the corrosion resistance of the alloy, rather than on the mechanical properties of the alloy. Impurities generally known include Fe, Ni, and Cu. Although Cu has adverse effects on corrosion resistance in Mg-Al-based alloys widely used, it has no significant effect in the Mg-Zn-based alloy according to the present invention. In association with the Mg-Zn-based alloy according to the present invention, Fe and Ni are regarded as impurities to be limited in their contents. Typically, these impurities are conservatively limited to a maximum content of 0.005 Adverse effects resulting from Fe may be eliminated by an addition of Mn. In the case of Mg alloys, adverse effects of Fe can be minimized by the reduction of the content ratio between Fe and Mn, Fe/Mn, to 0.032 or less. Since Mn is basically added in accordance with the present invention, it is possible to effectively eliminate adverse effects of Fe on corrosion resistance in so far as the content of Fe is less than the conservative limit. In the case of Mg alloys, the remaining impurities including Fe, Ni, and Cu are typically limited to a maximum content of 0.3 WO 02/27053 PCT/KR00/01072 wt.% based on the total content thereof.

The preparation method of the present invention, which uses a fluxless melting method in addition to the above mentioned specific composition, has an important feature in that Mn is added in the form of a Zn-Mn mother alloy, taking into consideration of the fact that it is impossible to add Mn to molten magnesium using a method of directly melt Mn into the molten magnesium, because Mn has a very high melting point. At an early stage of the development of magnesium alloys, a method was used in which Mn is added in the form of a flux. Since molten magnesium involves a danger of burning when it is exposed to air, a flux is used which serves to shield the molten magnesium from air, thereby inhibiting the danger of burning. For such a flux, an Mn-added flux is conventionally used to achieve a desired addition of Mn. In this case, Mn is penetrated into the melt by diffusion. In this method, there is a limitation on the amount of Mn added.

Furthermore, it is difficult to control the content of impurities. Thus, this method involves many difficulties associated with the preparation of an intended alloy. After the generalization of fluxless melting methods, in that the surface of the melt is covered by protective gas, addition of Mn was achieved, mainly using a method in which Mn is added in the form of a Mg- Mn mother alloy. In accordance with this method, Mn is added to molten magnesium heated to a temperature, at which Mn melts directly, in a protective gas atmosphere capable of preventing the molten magnesium to burn. Thus, an Mg-Mn mother alloy is separately prepared. In the alloy preparation using the fluxless melting method, a desired amount of Mn is added using the prepared Mg-Mn mother alloy. However, this method WO 02/27053 PCT/KR00/01072 requires an expensive melting device configured to control the given atmosphere. Furthermore, a large amount of magnesium may be lost during the preparation of the mother alloy, because magnesium exhibits a high vapor pressure at a high temperature. Thus, the method using the Mg-Mn mother alloy involves an increase in the processing costs. After a series of experiments, the inventors found that, in the alloy preparation using the fluxless melting method, addition of Mn can be effectively achieved using a method in which Mn is added to molten magnesium in the form of a lowmelting-point Zn-Mn mother alloy. In accordance with this method, it is possible to eliminate the burning possibility of the magnesium melt or a great loss of material. Accordingly, an economical preparation of magnesium alloys is possible. It is also possible to easily and conveniently control the content of impurities.

Preferably, the temperature of the magnesium melt, to which the Zn- Mn mother alloy is added, is limited to a range of 670 to 720"C, taking into consideration of the fact that although the melting point of magnesium is about 6500C, the magnesium melt secures a sufficient fluidity at a temperature of at least 6700C, and the fact that there is an increased possibility of burning at a temperature of the magnesium melt exceeding 720"C. The Zn-Mn mother alloy preferably has a Zn-10 20 wt.% Mn composition having an Mn content of 10 to 20 wt.% so that it is sufficiently melted in the above mentioned temperature range of the magnesium melt.

More preferably, a stirring process is carried out during the addition of the Zn-Mn mother alloy to the magnesium melt.

Si is added in the form of an Mg-Si mother alloy. Preferably, the WO 02/27053 PCT/KR00/01072 temperature, at which the addition of Si is carried out, is limited to a range of 700 to 720°C, taking into consideration of a high melting point of the mother alloy and a desired inhibition of burning at the surface of the magnesium melt. In this case, it is more preferable to conduct a stirring process during the addition of the mother alloy.

For a shortage of zinc, Zn is added alone or along with Al. At this time, Ca may be selectively added. Preferably, the addition of Zn is carried out after a furnace cooling process conducted for the magnesium melt, in order to reduce the loss of Zn exhibiting a high vapor pressure at the alloy preparation temperature used. The furnace cooling may be carried out to a temperature of about 670 0 C, taking into consideration of the fluidity of the magnesium melt. It is more preferable to conduct a stirring process during the addition of those elements.

The resultant Mg melt is then cast to form an ingot. Preferably, the casting is conducted after the Mg melt is furnace-cooled to a temperature of 660 to 670'C, in order to inhibit the generation of heat from the Mg melt as much as possible.

Preferably, the cast alloy ingot prepared in accordance with the above mentioned method is subjected to a homogenization treatment in order to eliminate segregation of alloying elements possibly generated during the casting process, and non-uniformity of the wrought body, in terms of properties, resulting from the segregation. The homogenization treatment is carried out at a temperature of 340 to 410'C for 6 to 12 hours, taking into consideration of conditions capable of allowing precipitation phases resulting from the major alloying element, that is, Zn, to be sufficiently dissolved, and WO 02/27053 PCT/KR00/01072 a desired thermal stability of the alloy.

Thereafter, the cast ingot is formed into a billet to be extruded.

Preferably, the billet is preheated at a temperature of 150 to 4000C for minutes to 2 hours, and then subjected to mechanical working processes including extrusion, rolling, forging, swaging, and drawing, in the same temperature range. Generally, magnesium alloys do not have a desired workability at ambient temperature. In order to obtain a sound wrought body, accordingly, the magnesium alloy is subjected to hot mechanical working processes. In accordance with the present invention, the working temperature is experimentally determined to be within a range capable of securing the soundness of the wrought body.

Preferably, the wrought body is primarily aged at a temperature of to 1000C for 24 to 96 hours, and secondarily aged, just after the primary aging process, at a temperature of 150 to 1800C for 48 hours or more. Such a double aging process is adapted to maximize the effect of the precipitation phase contributing to an improvement in strength by conducting the primary aging process at a temperature not higher than the G. P. zone solvus temperature of the predominant precipitation phase of Mg-Zn-based alloys, that is, the i31' phase, and then conducting the secondary aging process at a temperature higher than the primary aging temperature. In accordance with the present invention, therefore, the primary aging temperature is limited to a range of 70 to 1000C slightly lower than the generally-known G. P. zone solvus temperature of the 3i' phase, and the primary aging time is determined to be a period of time enough to expect an improvement in hardness to a desired level. Also, the second aging temperature is limited to WO 02/27053 PCT/KR00/01072 a range of 150 to 180 0 C. At a second aging temperature of less than 1500C, there is a problem associated with the execution of the aging process because a lot of time is required until a maximum hardness is obtained. At a second aging temperature exceeding 180'C, the maximum hardness obtained cannot reach a desired level even though it is rapidly obtained.

More preferably, the wrought body is subjected, prior to the double aging process, to a solution heat treatment for 6 to 12 hours at a temperature of 340 to 410'C corresponding to a temperature range, in which precipitation phases possibly generated during the working process can be present in the form of solid solutions, in order to maximize the effect of the precipitation phase contributing to an improvement in strength. The temperature range and period of the solution heat treatment are determined, based on the phase diagram of the Mg-Zn binary system, taking into consideration of conditions capable of allowing precipitation phases resulting from the major alloying element, that is, Zn, to be sufficiently dissolved, and a desired thermal stability of the alloy.

Meanwhile, it is more preferable to conduct a stretching process, prior to the double-aging process. Generally, the amount of stretching in a working process involving a heat treatment to strengthen a subject alloy is limited to a range from an elastic limit to a maximum strength limit, based on a strain measured by a tensile test for the alloy conducted before the heat treatment. In accordance with the present invention, therefore, the amount of stretching is limited to a range of 3 to 7 In accordance with the present invention, it is possible to prepare an inexpensive high strength magnesium alloy having an improved elongation WO 02/27053 PCT/KR00/01072 compared to the strength, compared to existing commercial wrought alloys.

That is, the magnesium alloy of the present invention can exhibit an elongation improved by two times or more over the maximum strength one of the existing commercial extruded alloys described in Table 1, that is, a ZC71 alloy, while maintaining a strength level similar to that of the ZC71 alloy. In accordance with the present invention, it is also possible to prepare a high strength alloy without using expensive alloying elements having a difficulty in handling, for example, a radioactive element such as Th, or alloying elements involving a difficulty in addition in association with the preparation process, for example, Zr. In accordance with the present invention, it is possible to reduce the loss of materials, and thus to reduce the preparation cost, because Mn is added in the form of a Zn-Mn mother alloy, compared to conventional methods in which Mn is added in the form of an Mg-Mn mother alloy.

BRIEF DESCRIPTION OF THE DRAWINGS The above objects, and other features and advantages of the present invention will become more apparent after a reading of the following detailed description when taken in conjunction with the drawings, in which: Fig. la is a photomicrograph of an Mg-Zn-based binary alloy extruded product (Z6); Figs. lb and ic are photomicrographs of respective extruded products of an Mg-Zn-based alloy added with Mn and an Mg-Zn-based alloy added with Al and Mn (ZM61 and ZAM621); Figs. Id and le are photomicrographs of respective extruded WO 02/27053 PCT/KR00/01072 products of an Mg-Zn-based alloy added with Al, Mn and Si, and an Mg-Znbased alloy added with Al, Mn, Si and Ca (ZAM631 2.5Si, and ZAM631 0.4Ca); Fig. 2 is a graph depicting the age hardening behavior of the Mg-Znbased binary alloy extruded product (Z6) exhibited during an aging process; Fig. 3 is a graph depicting a comparison of respective age hardening behaviors of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited during a double aging process with the age hardening behavior of the Mg-Zn-based binary alloy extruded product (Z6) exhibited during a double aging process; Fig. 4 is a graph depicting a comparison of respective age hardening behaviors of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited during a double aging process following a solution heat treatment with the age hardening behavior of the Mg-Zn-based binary alloy extruded product (Z6) exhibited when the same treatment is conducted; Fig. 5 is a graph depicting respective age hardening behaviors of the Al Mn Si-added Mg-Zn-based alloy extruded product (ZAM631 and Al Mn Si Ca-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si 0.4Ca) exhibited during a double aging process; Fig. 6 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature with the tensile properties of the WO 02/27053 PCT/KR00/01072 Mg-Zn-based binary alloy extruded product (Z6) exhibited at ambient temperature; Fig. 7 is a graph depicting respective tensile properties of the Al Mn Si-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si) and Al Mn Si Ca-added Mg-Zn-based alloy extruded product (ZAM631 0.4Ca) exhibited at ambient temperature; Fig. 8 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature after a double aging process with the tensile properties of the Mg-Zn-based binary alloy extruded product (Z6) exhibited at ambient temperature after the double aging process; Fig. 9 is a graph depicting respective tensile properties of the Al Mn Si-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si) and Al Mn Si Ca-added Mg-Zn-based alloy extruded product (ZAM631 0.4Ca) exhibited at ambient temperature after a double aging process; Fig. 10 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature after a double aging process following a solution heat treatment with the tensile properties of the Mg-Znbased binary alloy extruded product (Z6) exhibited at ambient temperature when the same treatment is conducted; and Fig. 11 is a graph depicting a comparison of respective tensile WO 02/27053 PCT/KR00/01072 properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature after a double aging process following a 5% stretching process with the tensile properties of the Mg-Znbased binary alloy extruded product (Z6) exhibited at ambient temperature when the same treatment is conducted.

BEST MODE FOR CARRYING OUT THE INVENTION Now, the high strength magnesium alloy according to the present invention will be described in more detail, with reference to the following examples.

Examples 1 to 11 In accordance with the present invention, alloy cast products were prepared which have rated compositions described in the following Table 2, respectively. In the preparation of each alloy cast product, melting of a raw alloy and alloying elements was achieved using a fluxless melting method in which a mixture gas of C02 0.5 SF6 is sprayed over the surface of the melt at a flow rate of 2 e/minute. A steel crucible was also used in the melting process. Mn was added in the form of a Zn-15 wt.% Mn mother alloy to the melt at a temperature of 700 0 C. Thereafter, the melt was stirred for minutes using a stirrer, and then cooled to 670°C in a furnace cooling fashion. The cooled melt was added with Zn alone or along with Al, and then stirred for 2 minutes. In the case involving an addition of Si, this Si was added in the form of an Mg-10 wt.% Si mother alloy to the melt. In this case, WO 02/27053 PCT/KR00/01072 the resultant melt was then stirred at 720 0 C for 10 minutes. After the completion of the stirring process, the melt was cooled to 670°C in a furnace cooling fashion. The cooled melt was added with Zn alone or along with Al and/or Ca, and then stirred for 2 minutes. Thereafter, the melt was furnacecooled to 660 0 C. Finally, the crucible was completely dipped in water maintained at ambient temperature. Thus, an alloy cast product was prepared.

Table 2 Rated Compositions of Alloys of Examples Rated Composition (wt%) Example Alloys Zn Al Mn Si Ca Mg 1 Z6 6 bal.

2 ZM60 6 0.5 bal.

3 ZM61 6 1 bal.

4 ZM62 6 1.5 bal.

ZAM611 6 1 1 bal.

6 ZAM621 6 2 1 bal.

7 ZAM631 6 3 1 bal.

8 ZAM641 6 4 1 bal.

9 ZAM661 6 6 1 bal.

ZAM631+2.5Si 6 3 1 2.5 bal.

11 ZAM631+2.5Si+0.4Ca 6 3 1 2.5 0.4 bal.

WO 02/27053 PCT/KR00/01072 In order to control the microstructure of each alloy cast product prepared as above, the alloy cast product was subjected to a homogenization process at a temperature of 340 to 410°C for 12 hours. The alloy cast product was then formed into a billet, which was, in turn, preheated at a temperature of 320 to 360'C for 30 minutes. The billet was then extruded by an extrusion machine, in which the temperature of the billet container and die was set to a temperature of 320 to 360°C. Thus, an extruded alloy product was prepared.

Figs. la, 1b, and 1c are photomicrographs of Z6, ZM61, and ZAM621 alloy extruded products prepared as mentioned above, respectively. Figs. ld and le are photomicrographs of ZAM631 2.5Si and ZAM631 2.5Si 0.4Ca alloy extruded products, respectively. Referring to Figs. la to le, the Z6 alloy, which is a conventional magnesium alloy, has a grain size of about 22 pm, whereas the ZM61 and ZAM621 alloys according to the present invention have grain sizes of about 12 pm and about 8 pm, respectively. The ZAM631 2.5Si and ZAM631 2.5Si 0.4Ca alloys have grain sizes of about 12 pm and about 6 pm, respectively.

Accordingly, it can be found that when Mn is added in an amount of 1 wt.% to the conventional Mg-Zn alloy, the microstructural grain size of the alloy is reduced by about 1/2. It can also be found that the conventional Mg- Zn alloy is added with 1 wt.% Mn and 2 wt.% Al, its grain size is reduced by about 1/3. In the case of the ZAM631 2.5Si 0.4Ca alloy, that is, where 0.4 wt.% Ca is added to the ZAM631 2.5Si alloy, it has a grain size of about 6 pm corresponding to about 2/3 the grain size of the ZAM621 alloy.

Consequently, it can be found that in the alloys according to the present WO 02/27053 PCT/KR00/01072 invention, a grain size reduction is obtained by about 2/3 for those added with Mn and Al and about 3/4 for those added with Si and Ca along with Mn and Al.

Fig. 2 is a graph depicting the age hardening behavior of the Mg-Znbased binary alloy extruded product (Z6) exhibited during an aging process.

For the Z6 alloy extruded product, a single aging process and a double aging process were carried out to obtain maximized improvements in hardness and strength, respectively. The Z6 alloy extruded product was primarily aged at 90'C for 48 hours, and then secondarily aged at 180'C for 384 hours under the condition in which a variation in age hardening behavior was periodically measured within the secondary aging period. The measured age hardening behavior variation is depicted in Fig. 2. Referring to Fig. 2, it can be found that the alloy subjected to the double aging treatment exhibits an increase in maximum hardness and a reduction in the time taken to obtain a maximum hardness, compared to the alloy subjected to the single aging treatment.

Fig. 3 is a graph depicting a comparison of respective age hardening behaviors of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited during a double aging process with the age hardening behavior of the Mg-Zn-based binary alloy extruded product (Z6) exhibited during the double aging process. Each of the Z6, ZM61, and ZAM621 alloy extruded products was primarily aged at 70'C for 48 hours, and then secondarily aged at 150 0 C for 384 hours under the condition in which a variation in age hardening behavior was periodically measured within the WO 02/27053 PCT/KR00/01072 secondary aging period. The measured age hardening behavior variation is depicted in Fig. 3. Referring to Fig. 3, it can be found that the ZAM621 alloy prepared by adding 2 wt.% Al and 1 wt.% Mn to the Z6 alloy exhibits an improvement in hardness by about 35 in an extruded state, and by about 20 in a state subjected to a maximum double age treatment, compared to the Z6 alloy. However, the ZM61 alloy prepared by adding only Mn to the Z6 alloy exhibited no or little hardening effect during the aging period even though it exhibited a high hardness in an extruded state. Also, the maximum hardness of the ZM61 alloy was lower than that of the Z6 alloy.

Fig. 4 is a graph depicting a comparison of respective age hardening behaviors of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited during a double aging process following a solution heat treatment with the age hardening behavior of the Mg-Zn-based binary alloy extruded product (Z6) exhibited when the same treatment is conducted.

Each of the Z6, ZM61, and ZAM621 alloy extruded products was first subjected to a solution heat treatment for 12 hours under the condition in which it was maintained at a temperature of 380 to 410 0 C. Following the solution heat treatment, each alloy was subjected to a double aging treatment. The age hardening behavior of each alloy resulting from the double aging treatment is depicted in Fig. 4. Referring to Fig. 4, it can be found that where the Z6 alloy is added with Mn alone or along with Al, it substantially exhibits an improvement in hardness during the age hardening process. The addition of the alloying element or elements contributed to an improvement in hardness by 10 or more, based on the maximum WO 02/27053 PCT/KR00/01072 hardness. In particular, the age hardening behavior of the ZM61 alloy prepared only by an addition of Mn was considerably different from the age hardening behavior exhibited under the heat treatment condition involving no solution heat treatment followed by the double aging treatment in that a remarkable improvement in hardness was obtained. The maximum hardness of the ZM61 alloy was similar to the ZAM621 alloy prepared by adding both Al and Mn.

Fig. 5 is a graph depicting respective age hardening behaviors of the Al Mn Si-added Mg-Zn-based alloy extruded product (ZAM631 and Al Mn Si Ca-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si 0.4Ca) exhibited during a double aging process. After being extruded, each of the ZAM631 2.5Si and ZAM631 2.5Si 0.4Ca alloys was primarily aged at 70 0 C for 48 hours, and then secondarily aged at 150 0 C for a given period of time under the condition in which a variation in age hardening behavior was periodically measured within the secondary aging period. Referring to Figs. 3 and 5, it can be found that the addition of wt.% Si and 0.4 wt.% Ca to the ZAM631 alloy results in an improvement in hardness by about 12 and a considerable reduction in the time taken to obtain a maximum hardness under the condition in which the alloy is subjected to a maximum double aging treatment at 150 0

C.

Table 3 Yield Strength Tensile Elongation Alloys (Mpa) strength WO 02/27053 PCT/KR00/01072 (Mpa) Z6 126 292 28 211 309 26 ZM61 223 313 26 ZM62 220 314 24 ZAM611 188 319 28 ZAM621 178 338 27 ZAM631 169 356 ZAM641 185 364 26 ZAM661 225 359 26 ZAM631+2.5Si 143 271 ZAM631+2.5Si+0.4Ca 150 371 16 Fig. 6 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature with the tensile properties of the Mg-Zn-based binary alloy extruded product (Z6) exhibited at ambient temperature. Referring to Fig. 6, it can be found that the addition of Mn alone or along with Al to the Z6 alloy results in a considerable increase in the yield strength and maximum tensile strength exhibited in an extruded state. In a wrought state using an extrusion process, the alloy exhibited a superior elongation of 25 or more. Detailed results are described in the above Table 3.

Fig. 7 is a graph depicting respective tensile properties of the Al WO 02/27053 PCT/KR00/01072 Mn Si-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si) and Al Mn Si Ca-added Mg-Zn-based alloy extruded product (ZAM631 0.4Ca) exhibited at ambient temperature. Referring to Fig. 7, it can be found that the addition of 2.5 wt.% Si and 0.4 wt.% Ca to the ZAM631 alloy results in an increase in the maximum tensile strength exhibited in an extruded state. In a wrought state using an extrusion process, the alloy exhibited a superior elongation of 16 or more. Detailed results are described in the above Table 3.

Table 4 Tensile Yield Strength Elongation Alloys Strength (Mpa) (Mpa) Z6 237 314 26 248 305 26 ZM61 253 314 28 ZM62 248 307 24 ZAM611 281 344 23 ZAM621 265 360 ZAM631 245 385 27 ZAM641 255 387 22 ZAM661 256 355 22 ZAM631+2.5Si 265 317 7 ZAM631+2.5Si+0.4Ca 234 398 12 WO 02/27053 PCT/KR00/01072 Fig. 8 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature after a double aging process with the tensile properties of the Mg-Zn-based binary alloy extruded product (Z6) exhibited at ambient temperature after the double aging process. Each of the Z6, ZM61, and ZAM621 alloys was primarily aged at 70°C for 48 hours, and then secondarily aged at 150°C for 96 hours. The tensile properties of each alloy, exhibited after the double aging process, are depicted in Fig. 8. Referring to Fig. 8, it can be found that the case involving the double aging treatment exhibits an increase in the yield strength and maximum tensile strength of each alloy, compared to the case involving no double aging treatment. It can also be found that both cases exhibit similar elongations, respectively. The tensile properties of each alloy, exhibited after a tensile test conducted following the double aging treatment, are described in the above Table 4.

Fig. 9 is a graph depicting respective tensile properties of the Al Mn Si-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si) and Al Mn Si Ca-added Mg-Zn-based alloy extruded product (ZAM631 2.5Si 0.4Ca) exhibited at ambient temperature after a double aging process. Each extruded alloy product was primarily aged at 70 0 C for 48 hours, and then secondarily aged at 150°C for 24 hours. The tensile properties of each alloy, exhibited after the double aging process, are depicted in Fig. 9. Referring to Fig. 9, it can be found that the extruded products of the ZAM631 2.5Si and ZAM631 +2.5Si 0.4Ca alloys WO 02/27053 PCT/KR00/01072 respectively prepared by adding 2.5 wt.% Si and a mixture of 2.5 wt.% Si and 0.4 wt.% Ca to the ZAM631 alloy obtain effects of considerably increased yield strength and maximum tensile strength, compared to those subjected to no double aging treatment. Detailed results are described in the above Table 4.

Referring to Table 4, it can be found that the ZM61 alloy prepared by adding Mn to the Z6 alloy exhibits a slight increase in tensile properties by virtue of the double aging treatment, compared to the Z6 alloy. The ZAM621 alloy prepared by adding both Al and Mn to the Z6 alloy exhibited a superior strength over the Z6 alloy, by virtue of the double aging treatment. In particular, the ZAM621 alloy exhibits a remarkable increase in maximum tensile strength. All alloys exhibit a superior elongation even after the double aging treatment.

Fig. 10 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature after a double aging process following a solution heat treatment with the tensile properties of the Mg-Znbased binary alloy extruded product (Z6) exhibited at ambient temperature when the same treatment is conducted. Each of the Z6, ZM61, and ZAM621 alloy extruded products was first subjected to a solution heat treatment for 12 hours at a temperature of 380 to 410'C. Following the solution heat treatment, each alloy extruded product was primarily aged at 70'C for 48 hours, and then secondarily aged at 150'C for 96 hours. The tensile properties of each alloy, exhibited after the double aging process, are WO 02/27053 PCT/KR00/01072 depicted in Fig. 10. Referring to Fig. 10, it can be found that when the solution heat treatment is carried out prior to the double aging treatment, the ZM61 alloy exhibits a considerable increase in yield strength and maximum tensile strength while exhibiting an elongation similar to that of the Z6 alloy.

Although the ZAM621 alloy exhibited a reduced yield strength, compared to the ZM61 alloy, it was similar to the ZM61 alloy in terms of the maximum tensile strength. In particular, the ZMA621 alloy exhibited a considerable increase in elongation. The tensile properties of each alloy exhibited at ambient temperature after the double aging treatment following the solution heat treatment are described in the following Table Table Tensile Yield Strength Elongation Alloys Strength (Mpa) (Mpa) Z6 252 310 16 331 349 13 ZM61 344 363 ZM62 339 358 13 ZAM611 295 349 22 ZAM621 252 361 23 ZAM631 239 391 23 ZAM641 254 400 21 ZAM661 232 408 WO 02/27053 PCT/KR00/01072 Meanwhile, a comparison was made between the case, in which each alloy extruded product is subjected to a double aging process just after the extrusion thereof, and the case in which the alloy extruded product is subjected to the double aging process following a solution heat treatment.

Based on the results of the comparison, it can be found that the ZM61 alloy exhibits a considerable increase in strength by virtue of the solution heat treatment followed by the dbuble aging process whereas the Z6 and ZAM621 alloys exhibit a slight strength increase under the same treatment conditions. It can also be found that the Z6 and ZM61 alloys exhibit a considerable reduction in elongation by virtue of the solution heat treatment followed by the double aging process whereas the ZAM621 alloy exhibit a similar elongation even after the solution heat treatment.

Fig. 11 is a graph depicting a comparison of respective tensile properties of the cast products of the Mn-added Mg-Zn-based alloy extruded product (ZM61) and Al Mn-added Mg-Zn-based alloy extruded product (ZAM621) exhibited at ambient temperature after a double aging process following a 5% stretching process with the tensile properties of the Mg-Znbased binary alloy extruded product (Z6) exhibited at ambient temperature when the same treatment is conducted. Each of the Z6, ZM61, and ZAM621 alloy extruded products was first subjected to a 5 stretching process.

Following the stretching process, each extruded alloy product was primarily aged at 70'C for 48 hours, and then secondarily aged at 150'C for 96 hours.

The tensile properties of each alloy, exhibited after the double aging process, are depicted in Fig. 11. Referring to Fig. 11, it can be found that the ZAM621 alloy exhibits an improvement in strength, compared to the case WO 02/27053 PCT/KR00/01072 involving no stretching process. The ZAM621 alloy also exhibited an elongation of 20 or more. All alloys substantially exhibited an improvement in strength by virtue of the stretching process followed by the double aging process. In particular, when the ZAM621 alloy was subjected only to the stretching process while being subjected to the solution heat treatment, prior to the double aging process, in order to obtain an improvement in strength, it exhibited a strength similar to that of the ZM61 alloy while exhibiting a great increase in elongation. The tensile properties of each alloy exhibited at ambient temperature after the double aging process following the 5 stretching process are described in the following Table 6.

Table 6 Alloys Z6 ZM61 ZM62 ZAM611 ZAM621 ZAM631 ZAM641 ZAM661 Yield Strength (Mpa) 298 311 314 297 337 318 316 315 314 Tensile Strength (Mpa) 336 337 347 327 376 377 405 403 386 Elongation 19 23 24 21 21 INDUSTRIAL APPLICABILITY As apparent from the above description, the present invention provides a magnesium alloy having improvements in the hardness and strength at ambient O temperature and an enhancement in elongation by adding Mn alone or along with Al to an Mg-Zn binary alloy while simultaneously adding Si alone or along with Ca 00 to the Mg-Zn binary alloy to prepare a wrought body having a reduced grain size, 00 11and conducting a heat treatment or a working process involving a heat treatment N for the wrought body.

The word 'comprising' and forms of the word 'comprising' as used in this description does not limit the invention claimed to exclude any variants or additions.

Although the preferred embodiments of the invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.

vlm MOl 1 673545v3 305162074

Claims

1. A high strength magnesium alloy consisting of 3 10 wt. Zn forming a C^ precipitation phase in the alloy, 0.25 3.0 wt. Mn present in the form of a-Mn in the alloy and refining the precipitation phase, and the balance of Mg and impurities. 00 00

2. The high strength magnesium alloy according to claim 1, further comprising 1 6 wt. Al.

3. The high strength magnesium alloy according to claim 2, further C comprising. 0.1 4.0 wt. Si

4. The high strength magnesium alloy according to claim 3, further comprising 0.1 2.0 wt. Ca.

The high strength magnesium alloy according to claim 2, wherein the content of Al is not more than the content of Zn.

6. The high strength magnesium alloy according to any one of claims 1 to wherein the content of Zn is 5.0 7.0 wt.

7. The high strength magnesium alloy according to any one of claims .1 to wherein the content of Mn is 0.75 2.0 wt

8. The high strength magnesium alloy according to claim 3 or 4, wherein the content of Si is 1.5 3.0 wt.

9. The high strength magnesium alloy according to claim 4, wherein the. content of Ca is 0.3 1.0 wt.

A method for preparing a high strength magnesium alloy according to any one of claims 1 to 9, wherein Mn is added in the form of a Zn-Mn mother alloy to a magnesium melt.

.11. The method according to claim 10, comprising the steps of: adding a Zn-10 20 wt. Mn mother alloy to the magnesium melt at a temperature of 670 to 720°C; adding Zn alone or along with Al to the magnesium melt; and forming the resultant magnesium melt into a cast body. tvlm M01 11673545v4 305162074 c

12. The method according to claim 10, comprising the steps of:' adding a Zn-10 20 wt. Mn mother alloy to the magnesium melt at a temperature of 670 to 720'C; adding an Mg-Si mother alloy to the magnesium melt; adding Zn alone or along with Al and/or Ca to the magnesium melt; and 00 00 11forming the resultant magnesium melt into a cast body. tr- N

13. The method according to claim 11 or 12, wherein the step of adding Zn alone or along with Al is carried out under a condition in which the magnesium melt has been cooled in a furnace cooling fashion to reduce a loss of Zn exhibiting a high vapor pressure at a temperature at which the alloy is prepared.

14. The method according to claim 11 or 12, further comprising the steps of: subjecting the cast body to a homogenization process at a temperature of 340 to 410' C for 6 to 12 hours; forming the cast body into a billet; preheating the billet at a temperature of 150 to 400°C for 30 minutes to 2 hours; and working the billet, thereby forming a wrought body.

The method according to claim 14, further comprising the steps of: primarily aging the wrought body at a temperature of 70 to 100°C for 24 to 96 hours; and secondarily aging the primarily-aged wrought body at a temperature of 150 to 180°C for 48 hours or more.

16. The method according to claim 15, further comprising the step of: conducting a solution heat treatment for the wrouight body at a temperature of 340 to 410°C for 6 to 12.hours, prior to the double aging.

17. The method according to claim 15, further comprising the step of: conducting a stretching of 3 to 7% for the wrought body, prior to the double aging. SHIN, Kwang Seon 9 May, 2005 tvlmMO 11673545v3 305162074