[go: up one dir, main page]

CN104498792B - Quick-corrosion magnesium alloy product and preparation method thereof - Google Patents

Quick-corrosion magnesium alloy product and preparation method thereof Download PDF

Info

Publication number
CN104498792B
CN104498792B CN201410810629.2A CN201410810629A CN104498792B CN 104498792 B CN104498792 B CN 104498792B CN 201410810629 A CN201410810629 A CN 201410810629A CN 104498792 B CN104498792 B CN 104498792B
Authority
CN
China
Prior art keywords
magnesium
ingot
nickel
aluminum
zinc
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201410810629.2A
Other languages
Chinese (zh)
Other versions
CN104498792A (en
Inventor
田哿
唐平洋
谭昕洋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Qaidam Qinghai Qing Yuanfan Magnesium Technology Co Ltd
Engineering Technology Research Institute of Sinopec Southwest Oil and Gas Co
Original Assignee
Qinghai Tsaidam Qingyuan Magnesium Science & Technology Co ltd
Engineering Technology Research Institute of Sinopec Southwest Oil and Gas Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Qinghai Tsaidam Qingyuan Magnesium Science & Technology Co ltd, Engineering Technology Research Institute of Sinopec Southwest Oil and Gas Co filed Critical Qinghai Tsaidam Qingyuan Magnesium Science & Technology Co ltd
Priority to CN201410810629.2A priority Critical patent/CN104498792B/en
Publication of CN104498792A publication Critical patent/CN104498792A/en
Application granted granted Critical
Publication of CN104498792B publication Critical patent/CN104498792B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C23/00Alloys based on magnesium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C23/00Alloys based on magnesium
    • C22C23/02Alloys based on magnesium with aluminium as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C23/00Alloys based on magnesium
    • C22C23/04Alloys based on magnesium with zinc or cadmium as the next major constituent

Landscapes

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

Abstract

The invention relates to a fast corrosion magnesium alloy product, which comprises the following components in percentage by weight: 1-6% of aluminum, 1-6% of zinc, 1-3% of iron, 5-15% of copper, 0.1-1% of silver, 0.1-1.2% of nickel and the balance of magnesium. Meanwhile, the invention also discloses a preparation method of the alloy product. The invention fully utilizes the effects of aluminum and zinc elements to improve the strength and the hardness of the magnesium alloy, improves the corrosion rate by copper, iron, silver and nickel elements, and greatly improves the mechanical property and the corrosion rate by regulating and controlling the proportion of the metal elements, thereby achieving the purposes of being used as a structural member, protecting equipment and being capable of rapidly dissolving under specific conditions.

Description

一种快速腐蚀镁合金产品及其制备方法A kind of rapid corrosion magnesium alloy product and preparation method thereof

技术领域technical field

本发明涉及金属合金材料技术领域,尤其涉及一种快速腐蚀镁合金产品及其制备方法。The invention relates to the technical field of metal alloy materials, in particular to a rapid corrosion magnesium alloy product and a preparation method thereof.

背景技术Background technique

镁合金是以镁为基体,加入其他元素所组成的合金,其特点是密度小(1. 8g/cm3镁合金左右)、比强度高、弹性模量大、散热好、消震性好、承受冲击载荷能力比铝合金大,它是实用金属中的最轻的金属,高强度、高刚性。随着工业的发展,金属材料的用量越来越多,所以腐蚀与腐蚀防护问题变得越来越重要了。Magnesium alloy is an alloy composed of magnesium as the matrix and adding other elements. It is characterized by low density (about 1. 8g/cm3 magnesium alloy), high specific strength, large elastic modulus, good heat dissipation, good shock absorption, and The impact load capacity is greater than that of aluminum alloy, it is the lightest metal among practical metals, with high strength and high rigidity. With the development of industry, more and more metal materials are used, so the problem of corrosion and corrosion protection becomes more and more important.

金属的腐蚀有很多种,电化学腐蚀是其中最重要的腐蚀之一,而阴极保护是一种重要的金属电化学腐蚀防护方法,使金属设备阴极极化而得到保护。牺牲阳极保护法的优点是不需要外加电源、不会干扰邻近金属设施、电流分散能力好、易于管理和维护等,因而得到了广泛的应用,There are many kinds of metal corrosion, electrochemical corrosion is one of the most important corrosion, and cathodic protection is an important metal electrochemical corrosion protection method, which can protect metal equipment by cathodic polarization. The advantage of the sacrificial anode protection method is that it does not require an external power supply, does not interfere with adjacent metal facilities, has good current dispersion capabilities, and is easy to manage and maintain, so it has been widely used.

但是对于市场上现有的镁合金材料而言,在中性环境条件下并不能满足某些特殊要求,比如快速腐蚀的材料,这使得迫切研发一种特殊镁合金来满足这种需求。However, for the existing magnesium alloy materials on the market, they cannot meet some special requirements under neutral environmental conditions, such as fast corrosion materials, which makes it urgent to develop a special magnesium alloy to meet this demand.

发明内容Contents of the invention

本发明所要解决的技术问题是提供一种力学性能和腐蚀速率均大幅度提高的快速腐蚀镁合金产品。The technical problem to be solved by the invention is to provide a rapidly corroded magnesium alloy product with greatly improved mechanical properties and corrosion rate.

本发明所要解决的另一个技术问题是提供该快速腐蚀镁合金产品的制备方法。Another technical problem to be solved by the present invention is to provide a preparation method for the rapid corrosion magnesium alloy product.

为解决上述问题,本发明所述的一种快速腐蚀镁合金产品,其特征在于:该合金产品由下述重量百分比的成分组成:1~6%的铝,1~6%的锌,1~3%的铁,5~15%的铜,0.1~1%的银,0.1~1.2%的镍,余量为镁。In order to solve the above problems, a kind of rapid corrosion magnesium alloy product according to the present invention is characterized in that: the alloy product is composed of the following components by weight percentage: 1~6% aluminum, 1~6% zinc, 1~6% 3% iron, 5~15% copper, 0.1~1% silver, 0.1~1.2% nickel, and the balance is magnesium.

如上所述的一种快速腐蚀镁合金产品的制备方法,包括以下步骤:A method for preparing a rapid corrosion magnesium alloy product as described above, comprising the following steps:

⑴对含30%铜的镁-铜合金进行预处理:将含30%铜的镁-铜合金切成20mm×20mm×20mm的小块,并按常规方法去除表面的氧化物和油污,再经无水酒精清洗干净后,在温度为101℃的条件下烘干至恒重,即得预处理后的镁-铜合金;⑴Pretreatment of magnesium-copper alloy containing 30% copper: Cut the magnesium-copper alloy containing 30% copper into small pieces of 20mm×20mm×20mm, and remove oxides and oil stains on the surface according to conventional methods, and then After cleaning with anhydrous alcohol, dry at a temperature of 101°C to constant weight to obtain the pretreated magnesium-copper alloy;

⑵对含50%镍的铝-镍合金进行预处理:将含50%镍的铝-镍合金切成10mm×10mm×10mm的小块,并按常规方法去除表面的氧化物和油污,再经无水酒精清洗干净后,在温度为101℃的条件下烘干至恒重,即得预处理后的铝-镍合金;⑵Pretreatment of aluminum-nickel alloy containing 50% nickel: Cut the aluminum-nickel alloy containing 50% nickel into small pieces of 10mm×10mm×10mm, remove oxides and oil stains on the surface according to conventional methods, and then After cleaning with anhydrous alcohol, dry at a temperature of 101°C to constant weight to obtain the pretreated aluminum-nickel alloy;

⑶分别对镁锭、铝锭、锌锭进行预处理:分别将镁锭、铝锭、锌锭切成100mm×50mm×20mm的小块,并按常规方法去除表面的氧化物和油污,再经无水酒精清洗干净后,在温度为101℃的条件下烘干至恒重,即分别得到预处理后的镁锭、铝锭、锌锭;(3) Pretreatment of magnesium ingots, aluminum ingots, and zinc ingots: respectively cut magnesium ingots, aluminum ingots, and zinc ingots into small pieces of 100mm×50mm×20mm, and remove oxides and oil stains on the surface according to conventional methods, and then After cleaning with anhydrous alcohol, dry at a temperature of 101°C to constant weight to obtain pretreated magnesium ingots, aluminum ingots, and zinc ingots;

⑷分别对铁粉和银粉进行预处理:分别将粒度≥100目的铁粉和银粉在温度为101℃的条件下烘干至恒重后,即分别得到干燥的铁粉和干燥的银粉;(4) Pretreatment of iron powder and silver powder respectively: after drying iron powder and silver powder with particle size ≥ 100 mesh at a temperature of 101°C to constant weight, respectively, dry iron powder and dry silver powder are obtained;

⑸采用常规方法,按1kg产品折算所述预处理后的镁锭、铝锭、锌锭及所述预处理后的镁-铜合金、所述预处理后的铝-镍合金、所述干燥的铁粉、所述干燥的银粉的用量,然后将它们依次加入到熔炼炉中,在惰性气体氩气的保护下升温至660~750℃使其熔化,并搅拌均匀,得到熔融物;所述熔融物在700℃~750℃保温25~35分钟后降温至660~700℃,并在该温度下静置10~20分钟后进行浇铸,得到铸锭,该铸锭自然冷却至室温,即得快速腐蚀镁合金产品。(5) Using conventional methods, convert the pretreated magnesium ingots, aluminum ingots, zinc ingots, and the pretreated magnesium-copper alloys, the pretreated aluminum-nickel alloys, and the dried The amount of iron powder and the dry silver powder, and then they are sequentially added to the smelting furnace, heated to 660~750°C under the protection of inert gas argon to melt, and stirred evenly to obtain the melt; the melt The material is kept at 700°C~750°C for 25~35 minutes, then cooled to 660~700°C, and cast at this temperature for 10~20 minutes to obtain an ingot, which is naturally cooled to room temperature, that is, fast Corrosion of magnesium alloy products.

所述镁锭、铝锭、锌锭、含30%铜的镁-铜合金、含50%镍的铝-镍合金均为工业级纯度及以上。The magnesium ingots, aluminum ingots, zinc ingots, magnesium-copper alloys containing 30% copper, and aluminum-nickel alloys containing 50% nickel are all of industrial grade purity and above.

铁粉、银粉均为工业级。Both iron powder and silver powder are industrial grade.

本发明与现有技术相比具有以下优点:Compared with the prior art, the present invention has the following advantages:

1、本发明充分利用铝和锌元素的作用来提高镁合金的强度和硬度,铜、铁、银、镍元素来提高腐蚀速率,通过调控金属元素之间的配比,使其力学性能和腐蚀速率均大幅度提高(参见表1,腐蚀速率的测试参照JB/T 7901-1999,具体条件为样块在60℃、3%的KCl溶液中测试),其抗拉强度300MPa以上,腐蚀速率为普通牺牲阳极镁合金的5倍以上,能满足某些特定施工所要求的性能,如油气田压裂施工、牺牲材料,从而达到即可作为结构件又能起到保护设备,在特定条件下还能自身快速溶解的目的。1. The present invention makes full use of the effects of aluminum and zinc elements to increase the strength and hardness of magnesium alloys, copper, iron, silver, and nickel elements to increase the corrosion rate, and adjusts the ratio between metal elements to make its mechanical properties and corrosion resistance The rates are greatly increased (see Table 1, the corrosion rate test refers to JB/T 7901-1999, the specific conditions are that the sample block is tested in 60 ° C, 3% KCl solution), its tensile strength is above 300 MPa, and the corrosion rate is It is more than 5 times that of ordinary sacrificial anode magnesium alloy, which can meet the performance required by certain specific constructions, such as oil and gas field fracturing construction, sacrificial materials, so as to be used as structural parts and protect equipment, and can also be used under certain conditions The purpose of self-dissolving quickly.

表1Table 1

具体实施方式detailed description

实施例1 一种快速腐蚀镁合金产品,该合金产品由下述重量百分比(g/g)的成分组成:1%的铝,6%的锌,1%的铁,10%的铜,0.1%的银,0.1%的镍,余量为镁。Example 1 A rapidly corroding magnesium alloy product, the alloy product is composed of the following components by weight percentage (g/g): 1% aluminum, 6% zinc, 1% iron, 10% copper, 0.1% of silver, 0.1% of nickel, and the balance of magnesium.

该快速腐蚀镁合金产品的制备方法,包括以下步骤:The preparation method of the rapid corrosion magnesium alloy product comprises the following steps:

⑴对含30%铜的镁-铜合金进行预处理:将含30%铜的镁-铜合金切成20mm×20mm×20mm的小块,并按常规方法去除表面的氧化物和油污,再经无水酒精清洗干净后,在温度为101℃的条件下烘干至恒重,即得预处理后的镁-铜合金。⑴Pretreatment of magnesium-copper alloy containing 30% copper: Cut the magnesium-copper alloy containing 30% copper into small pieces of 20mm×20mm×20mm, and remove oxides and oil stains on the surface according to conventional methods, and then After cleaning with anhydrous alcohol, dry at a temperature of 101° C. to constant weight to obtain the pretreated magnesium-copper alloy.

⑵对含50%镍的铝-镍合金进行预处理:将含50%镍的铝-镍合金切成10mm×10mm×10mm的小块,并按常规方法去除表面的氧化物和油污,再经无水酒精清洗干净后,在温度为101℃的条件下烘干至恒重,即得预处理后的铝-镍合金。⑵Pretreatment of aluminum-nickel alloy containing 50% nickel: Cut the aluminum-nickel alloy containing 50% nickel into small pieces of 10mm×10mm×10mm, remove oxides and oil stains on the surface according to conventional methods, and then After cleaning with anhydrous alcohol, dry at a temperature of 101° C. to constant weight to obtain the pretreated aluminum-nickel alloy.

⑶分别对镁锭、铝锭、锌锭进行预处理:分别将镁锭、铝锭、锌锭切成100mm×50mm×20mm的小块,并按常规方法去除表面的氧化物和油污,再经无水酒精清洗干净后,在温度为101℃的条件下烘干至恒重,即分别得到预处理后的镁锭、铝锭、锌锭。(3) Pretreatment of magnesium ingots, aluminum ingots, and zinc ingots: respectively cut magnesium ingots, aluminum ingots, and zinc ingots into small pieces of 100mm×50mm×20mm, and remove oxides and oil stains on the surface according to conventional methods, and then After cleaning with anhydrous alcohol, dry at a temperature of 101° C. to constant weight to obtain pretreated magnesium ingots, aluminum ingots, and zinc ingots.

⑷分别对铁粉和银粉进行预处理:分别将粒度≥100目的铁粉和银粉在温度为101℃的条件下烘干至恒重后,即分别得到干燥的铁粉和干燥的银粉。(4) Pretreatment of iron powder and silver powder respectively: after drying iron powder and silver powder with particle size ≥100 mesh at a temperature of 101°C to constant weight, dry iron powder and dry silver powder are respectively obtained.

⑸将预处理后的镁锭585g、铝锭9g、锌锭60g及预处理后的镁-铜合金333g、预处理后的铝-镍合金2g、干燥的铁粉10g、干燥的银粉1g依次加入到熔炼炉中,在惰性气体氩气的保护下升温至660~750℃使其熔化,并搅拌均匀,得到熔融物;所述熔融物在700℃~750℃保温25~35分钟后降温至660~700℃,并在该温度下静置10~20分钟后进行浇铸,得到铸锭,该铸锭自然冷却至室温,即得快速腐蚀镁合金产品。(5) Add 585g of pretreated magnesium ingot, 9g of aluminum ingot, 60g of zinc ingot, 333g of pretreated magnesium-copper alloy, 2g of pretreated aluminum-nickel alloy, 10g of dry iron powder, and 1g of dry silver powder in sequence In the smelting furnace, under the protection of inert gas argon, heat up to 660~750°C to melt, and stir evenly to obtain the melt; the melt is kept at 700°C~750°C for 25~35 minutes and then cooled to 660°C ~700°C, and cast at this temperature for 10-20 minutes to obtain an ingot. The ingot is naturally cooled to room temperature, and the rapid corrosion magnesium alloy product is obtained.

实施例2 一种快速腐蚀镁合金产品,该合金产品由下述重量百分比(g/g)的成分组成: 6%的铝,1%的锌,3%的铁,5%的铜,1%的银,1.2%的镍,余量为镁。Example 2 A rapidly corroding magnesium alloy product, the alloy product is composed of the following components by weight percentage (g/g): 6% aluminum, 1% zinc, 3% iron, 5% copper, 1% of silver, 1.2% of nickel, and the balance of magnesium.

该快速腐蚀镁合金产品的制备方法,包括以下步骤:The preparation method of the rapid corrosion magnesium alloy product comprises the following steps:

⑴对含30%铜的镁-铜合金进行预处理同实施例1。(1) the magnesium-copper alloy containing 30% copper is pretreated with embodiment 1.

⑵对含50%镍的铝-镍合金进行预处理同实施例1。(2) Pretreatment is carried out with embodiment 1 to the aluminum-nickel alloy containing 50% nickel.

⑶分别对镁锭、铝锭、锌锭进行预处理同实施例1。(3) Carry out pretreatment to magnesium ingot, aluminum ingot, zinc ingot respectively with embodiment 1.

⑷分别对铁粉和银粉进行预处理同实施例1。(4) Carry out pretreatment with embodiment 1 to iron powder and silver powder respectively.

⑸将预处理后的镁锭711g、铝锭48g、锌锭10g及预处理后的镁-铜合金167g、预处理后的铝-镍合金24g、干燥的铁粉30g、干燥的银粉10g依次加入到熔炼炉中,在惰性气体氩气的保护下升温至660~750℃使其熔化,并搅拌均匀,得到熔融物;所述熔融物在700℃~750℃保温25~35分钟后降温至660~700℃,并在该温度下静置10~20分钟后进行浇铸,得到铸锭,该铸锭自然冷却至室温,即得快速腐蚀镁合金产品。(5) Add 711g of pretreated magnesium ingot, 48g of aluminum ingot, 10g of zinc ingot, 167g of pretreated magnesium-copper alloy, 24g of pretreated aluminum-nickel alloy, 30g of dry iron powder, and 10g of dry silver powder in sequence In the smelting furnace, under the protection of inert gas argon, heat up to 660~750°C to melt, and stir evenly to obtain the melt; the melt is kept at 700°C~750°C for 25~35 minutes and then cooled to 660°C ~700°C, and cast at this temperature for 10-20 minutes to obtain an ingot. The ingot is naturally cooled to room temperature, and the rapid corrosion magnesium alloy product is obtained.

实施例3 一种快速腐蚀镁合金产品,该合金产品由下述重量百分比(g/g)的成分组成:3%的铝,3%的锌,2%的铁,15%的铜,0.5%的银,0.5%的镍,余量为镁。Example 3 A rapidly corroding magnesium alloy product, the alloy product is composed of the following components by weight percentage (g/g): 3% aluminum, 3% zinc, 2% iron, 15% copper, 0.5% of silver, 0.5% of nickel, and the balance of magnesium.

该快速腐蚀镁合金产品的制备方法,包括以下步骤:The preparation method of the rapid corrosion magnesium alloy product comprises the following steps:

⑴对含30%铜的镁-铜合金进行预处理同实施例1。(1) the magnesium-copper alloy containing 30% copper is pretreated with embodiment 1.

⑵对含50%镍的铝-镍合金进行预处理同实施例1。(2) Pretreatment is carried out with embodiment 1 to the aluminum-nickel alloy containing 50% nickel.

⑶分别对镁锭、铝锭、锌锭进行预处理同实施例1。(3) Carry out pretreatment to magnesium ingot, aluminum ingot, zinc ingot respectively with embodiment 1.

⑷分别对铁粉和银粉进行预处理同实施例1。(4) Carry out pretreatment with embodiment 1 to iron powder and silver powder respectively.

⑸将预处理后的镁锭410kg、铝锭25g、锌锭30g及预处理后的镁-铜合金500g、预处理后的铝-镍合金10g、干燥的铁粉20g、干燥的银粉5g依次加入到熔炼炉中,在惰性气体氩气的保护下升温至660~750℃使其熔化,并搅拌均匀,得到熔融物;所述熔融物在700℃~750℃保温25~35分钟后降温至660~700℃,并在该温度下静置10~20分钟后进行浇铸,得到铸锭,该铸锭自然冷却至室温,即得快速腐蚀镁合金产品。(5) Add 410kg of pretreated magnesium ingot, 25g of aluminum ingot, 30g of zinc ingot, 500g of pretreated magnesium-copper alloy, 10g of pretreated aluminum-nickel alloy, 20g of dry iron powder, and 5g of dry silver powder in sequence In the smelting furnace, under the protection of inert gas argon, heat up to 660~750°C to melt, and stir evenly to obtain the melt; the melt is kept at 700°C~750°C for 25~35 minutes and then cooled to 660°C ~700°C, and cast at this temperature for 10-20 minutes to obtain an ingot. The ingot is naturally cooled to room temperature, and the rapid corrosion magnesium alloy product is obtained.

上述实施例1~3中,镁锭、铝锭、锌锭、含30%铜的镁-铜合金、含50%镍的铝-镍合金均为工业级纯度及以上。铁粉、银粉均为工业级。In the above examples 1-3, magnesium ingots, aluminum ingots, zinc ingots, magnesium-copper alloys containing 30% copper, and aluminum-nickel alloys containing 50% nickel are all of industrial grade purity and above. Both iron powder and silver powder are industrial grade.

Claims (3)

1. a fast erosion magnesium-alloy material, it is characterised in that: this alloy product is grouped into by the one-tenth of following weight percentage ratio: The aluminum of 1 ~ 6%, the zinc of 1 ~ 6%, the ferrum of 1 ~ 3%, the copper of 5 ~ 15%, the silver of 0.1 ~ 1%, the nickel of 0.1 ~ 1.2%, surplus is magnesium;
Its preparation method, comprises the following steps:
(1) magnesium-the copper alloy containing 30% bronze medal is carried out pretreatment: the magnesium-copper alloy containing 30% bronze medal is cut into 20mm × 20mm × 20mm Fritter, and remove oxide and the greasy dirt on surface according to a conventional method, then after anhydrous alcohol cleans up, be 101 in temperature Dry under conditions of DEG C to constant weight, obtain pretreated magnesium-copper alloy;
(2) the aluminum-nickel alloy containing 50% nickel is carried out pretreatment: the aluminum-nickel alloy containing 50% nickel is cut into 10mm × 10mm × 10mm Fritter, and remove oxide and the greasy dirt on surface according to a conventional method, then after anhydrous alcohol cleans up, be 101 in temperature Dry under conditions of DEG C to constant weight, obtain pretreated aluminum-nickel alloy;
The most respectively magnesium ingot, aluminium ingot, zinc ingot metal are carried out pretreatment: respectively magnesium ingot, aluminium ingot, zinc ingot metal are cut into 100mm × 50mm × The fritter of 20mm, and remove oxide and the greasy dirt on surface according to a conventional method, then after anhydrous alcohol cleans up, in temperature be Dry to constant weight under conditions of 101 DEG C, i.e. respectively obtain pretreated magnesium ingot, aluminium ingot, zinc ingot metal;
The most respectively iron powder and argentum powder are carried out pretreatment: be 101 DEG C by the iron powder of granularity >=100 mesh and argentum powder in temperature respectively Under the conditions of dry to constant weight, i.e. respectively obtain dry iron powder and be dried argentum powder;
(5) use conventional method, convert described pretreated magnesium ingot, aluminium ingot, zinc ingot metal and described pretreated by 1kg product Magnesium-copper alloy, described pretreated aluminum-nickel alloy, described dry iron powder, the consumption of described dry argentum powder, then will They are added sequentially in smelting furnace, be warming up to 660 ~ 750 DEG C and make it melt under the protection of noble gas argon, and stir all Even, obtain fused mass;Described fused mass is cooled to 660 ~ 700 DEG C after being incubated 25 ~ 35 minutes at 700 DEG C ~ 750 DEG C, and in this temperature The lower standing of degree was cast after 10 ~ 20 minutes, obtained ingot casting, and this ingot casting naturally cools to room temperature, obtains fast erosion magnesium alloy Product.
2. fast erosion magnesium-alloy material as claimed in claim 1 a kind of, it is characterised in that: described magnesium ingot, aluminium ingot, zinc ingot metal, Magnesium-copper alloy containing 30% bronze medal, the aluminum-nickel alloy containing 50% nickel be technical grade purity and more than.
3. a kind of fast erosion magnesium-alloy material as claimed in claim 1, it is characterised in that: described iron powder, argentum powder are work Industry level.
CN201410810629.2A 2014-12-24 2014-12-24 Quick-corrosion magnesium alloy product and preparation method thereof Expired - Fee Related CN104498792B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410810629.2A CN104498792B (en) 2014-12-24 2014-12-24 Quick-corrosion magnesium alloy product and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410810629.2A CN104498792B (en) 2014-12-24 2014-12-24 Quick-corrosion magnesium alloy product and preparation method thereof

Publications (2)

Publication Number Publication Date
CN104498792A CN104498792A (en) 2015-04-08
CN104498792B true CN104498792B (en) 2016-08-17

Family

ID=52940242

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410810629.2A Expired - Fee Related CN104498792B (en) 2014-12-24 2014-12-24 Quick-corrosion magnesium alloy product and preparation method thereof

Country Status (1)

Country Link
CN (1) CN104498792B (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105478748B (en) * 2015-12-15 2018-08-28 青海柴达木青元泛镁科技有限公司 A kind of preparation method of the lightweight temporary plugging ball of high-strength, high instant capacity
CN105537865B (en) * 2015-12-15 2019-03-26 青海柴达木青元泛镁科技有限公司 A kind of preparation method of high-intensitive, low-density lightweight cycle frame
CN105543744B (en) * 2015-12-15 2018-12-11 青海柴达木青元泛镁科技有限公司 A kind of preparation method of high-intensitive, low-density lightweight unmanned plane wing
CN105499921A (en) * 2015-12-15 2016-04-20 青海柴达木青元泛镁科技有限公司 Preparation method of high-strength and high-instant-solubility light fracture ball
CN105950930B (en) * 2016-06-24 2018-02-06 中国石油集团川庆钻探工程有限公司长庆井下技术作业公司 A kind of solvable extruded Magnesium Alloy and preparation method thereof
CN110016598A (en) * 2019-04-14 2019-07-16 太原理工大学 A kind of high-strength rapid corrosion magnesium alloy and preparation method thereof
WO2021075552A1 (en) 2019-10-18 2021-04-22 株式会社栗本鐵工所 Degradable magnesium alloy
CN111218593B (en) * 2020-03-09 2021-02-02 厦门火炬特种金属材料有限公司 Preparation method of rapidly-dissolved magnesium alloy

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102586605A (en) * 2011-01-18 2012-07-18 华孚精密金属科技(常熟)有限公司 Method for recovering aluminum-containing magnesium alloy waste material
CN103343271A (en) * 2013-07-08 2013-10-09 中南大学 Light and pressure-proof fast-decomposed cast magnesium alloy

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02232332A (en) * 1989-03-07 1990-09-14 Tech Res & Dev Inst Of Japan Def Agency Highly corrosive magnesium alloy

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102586605A (en) * 2011-01-18 2012-07-18 华孚精密金属科技(常熟)有限公司 Method for recovering aluminum-containing magnesium alloy waste material
CN103343271A (en) * 2013-07-08 2013-10-09 中南大学 Light and pressure-proof fast-decomposed cast magnesium alloy

Also Published As

Publication number Publication date
CN104498792A (en) 2015-04-08

Similar Documents

Publication Publication Date Title
CN104498792B (en) Quick-corrosion magnesium alloy product and preparation method thereof
CN103255327B (en) Al-Zn-Mg-Cu-Mn-Zr-Er alloy and preparation technology
CN102618743A (en) Additive for aluminum alloy melting
WO2018095186A1 (en) Heat conductive aluminium alloy and use thereof
CN103695674B (en) A kind of titanium hydride and potassium fluoborate prepare the method for Al-Ti-B intermediate alloy
CN106676357B (en) A kind of high plastic magnesium alloy and preparation method thereof
CN105734375B (en) A kind of magnesium alloy sacrificial anode material containing Sb
CN101363093B (en) High-strength cast aluminium alloy material
CN104630586B (en) Flame-retardant and heat-resistant magnesium alloy and preparation method
CN103602865A (en) Copper-containing heat-resistant magnesium-tin alloy and preparation method thereof
CN103146973A (en) High-temperature-resistant rare earth magnesium alloy
CN105779837A (en) Gd containing sacrificial anode magnesium alloy
CN105316550A (en) High-damping magnesium alloy containing long-periodic structural phase and preparation method for high-damping magnesium alloy
CN102304651A (en) Casting aluminum-silicon alloy and strengthening method thereof
CN108715964B (en) A kind of rare earth magnesium alloy and preparation method thereof
CN110016598A (en) A kind of high-strength rapid corrosion magnesium alloy and preparation method thereof
CN104988347A (en) Refining agent for production of aluminum alloy sacrificial anodes, and preparation method thereof
CN104060280B (en) A kind of sacrificial aluminium alloy anode be applicable to abyssal environment with high current efficiency
CN103774019B (en) A kind of heat resistance magnesium alloy of stable high-temperature strength
CN104018163A (en) Novel alloy sacrificial anode
CN108559897B (en) A kind of high-strength corrosion-resisting magnesium alloy and preparation method thereof
Sun et al. Effects of double-procedure homogenization heat treatment on microstructure and mechanical properties of WE43A alloy
CN102965545A (en) Zinc alloy material
CN106167867A (en) A kind of rare-earth containing aluminium magnesium alloy electromagnetic shielding silk round wires
CN102051508A (en) Corrosion-resisting AZ91 magnesium alloy

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
ASS Succession or assignment of patent right

Owner name: QINGHAI TSAIDAM QINGYUAN MAGNESIUM SCIENCE + TECHN

Effective date: 20150410

Owner name: ENGINEERING TECHNOLOGY RESEARCH INSTITUTE OF SOUTH

Free format text: FORMER OWNER: QINGHAI TSAIDAM QINGYUAN MAGNESIUM SCIENCE + TECHNOLOGY CO., LTD.

Effective date: 20150410

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 817099 HAIXI MONGOL AND TIBETAN AUTONOMOUS PREFECTURE, QINGHAI PROVINCE TO: 618000 DEYANG, SICHUAN PROVINCE

TA01 Transfer of patent application right

Effective date of registration: 20150410

Address after: 618000 Deyang city of Sichuan province Longquan mountain road, No. 298

Applicant after: Engineering Technology Research Institute of Southwest Oil Gas Branch, SINOPEC

Applicant after: Qaidam, Qinghai Qing Yuanfan Magnesium Technology Co., Ltd

Address before: 817099 Qinghai Province, Jianshe Road Haixi Mongolian Tibetan Autonomous Prefecture of Delingha City, No. 1

Applicant before: Qaidam, Qinghai Qing Yuanfan Magnesium Technology Co., Ltd

C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20160817

Termination date: 20161224