US2101919A - Production of refined magnesium and magnesium alloys - Google Patents

Production of refined magnesium and magnesium alloys Download PDF

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Publication number
US2101919A
US2101919A US36853A US3685335A US2101919A US 2101919 A US2101919 A US 2101919A US 36853 A US36853 A US 36853A US 3685335 A US3685335 A US 3685335A US 2101919 A US2101919 A US 2101919A
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magnesium
metal
refined
alloys
production
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US36853A
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Schichtel Georg
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American Magnesium Metals Corp
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American Magnesium Metals Corp
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B26/00Obtaining alkali, alkaline earth metals or magnesium
    • C22B26/20Obtaining alkaline earth metals or magnesium
    • C22B26/22Obtaining magnesium

Definitions

  • This invention relates to, the production of refined magnesium and magnesium alloys.
  • the present invention is a continuation in part of my application Serial No. 706,558, filed January 13, 1934 for the Production of refined magnesium and magnesium alloys, which has since become Patent No. 2,066,579, dated Jan. 5, 1937.
  • One object of the present invention is to provide a simple and commerciallypracticable process for the production-of compact metallic magnesium in a substantially chemically pure state.
  • Another object of 'my invention is to enable magnesium and magnesium alloys respectively, to be recovered, in a refined state, from waste, such as for example scrap arising from machine working and casting of magnesium or its alloys, and thereby not only to obtain a purer product as a result of my improved process, but also to ensure great saving by increasing the quantity of the recoveries.
  • the present invention aims at enabling magnesium being technically pure' (and its alloys) to be very extensively refined in thesimplest manner.
  • the process is also admirably adapted for the elimination of impurities present during the recovery of magnesium by re-melting magnesium scrap (for example from machine working and from the foundry).
  • impurities present during the recovery of magnesium by re-melting magnesium scrap for example from machine working and from the foundry.
  • magnesium dross from which only 30% of the magnesium content could be recovered, as
  • the present invention enables up to 90% of the metal originally present to be recovered as metal free from slag.
  • This group cf.processes also includes the pro-' posal to refine magnesium by melting the metal in association with alkali chlorides (especially sodium chloride or potassium chloride) or mixtures of alkali chlorides, having melting points substantially higher than that of magnesium. These conditions are fulfilled by mixtures in which the sodium chloride or potassium chloride predominates. After melting, the 'whole is left to cool down to a temperature at which the salt, or saline mixture, has solidified to form a crust in which the impurities are occluded, whilst the metal is still fluid.
  • alkali chlorides especially sodium chloride or potassium chloride
  • mixtures of alkali chlorides having melting points substantially higher than that of magnesium.
  • Another group of processes consists in refining the metal by melting it in association with additions which lead to the formation of an alloy to a moderate extent. specified as an addition of this kind in United States specification No, 1,698,647, with the qualification that, as an alloying component, this metal exerts a highly unfavorable influence on the magnesium- (page 1, lines 41 to 58). ,For this reason, the specification recommends that, when magnesium fluoride is used as the main Zinc, for example, is
  • the magnesium, or material containing same, that is to be refined is melted in association with small per cents by weight (referred to the total weightof material under treatment) being usually sufiicient.
  • the melting point of the selected salt or saline mixture should preferably be lower than that of. magnesium, but the specific gravity higher than that of the molten metal. If such salts be strewn over the metal during the melting down process, they melt sooner than the metal and envelop it, thereby protecting it against oxidation. This behavior has a specially advantageous eifect in the case of magnesium alloys, their melting points being lower than that of the metal.
  • the higher specific gravity of thesaline melt causes it to subside quickly after absorption of the-impurities, so that, after settling, the refined metal can be poured off. Nevertheless the fused metal remains protected against oxidation by a supernatent thin film of the saline melt.
  • salt mixtures are th (19) Sb13+30% EeCl3+ 30% ZnCl2+30% MgClz sb2s3+30% FeCla-l- 30% ZnCla+2 0% MgCl:
  • magnesium in the following claims to include not only crude or technically p'ure magnesium metal but also magnesium alloys and magnesium waste arising for example from machine working or casting of magnesium or its alloys.
  • the method of producing refined magnesium which comprises melting impure magnesium with a fluid fluxcOntaining as purifying agents a mixture of antimony sulphide, chloride of iron, zinc chloride and magnesium chloride, agitating the molten metal with the flux, allowing the metal and the flux to segregate from eachother, and separating the metal from the flux.
  • the method of producing refined magnesium which comprises melting impure magnesium with a fluid flux consisting of. 40 per cent of antimony trisulphide, 20 per cent of iron chloride, 10 per cent of zinc chloride and 30 per cent of. magnesium chloride, agitating the molten metal with the flux, allowing the metal and the 4.
  • the method of refining magnesium whichcomprises melting impure magnesium with a fluid flux containing as the main purifier a salt '25 flux to segregate from each other, and separat- ,of antimony selected from the group consisting of antimony selected from the group consisting of halides and sulfides, further containing a salt selected from the group of halides of cadmium, copper, zinc and magnesium. and further containing a halide of iron, agitating the molten metal with the flux, allowing the metal and the .flux to segregate from each other and separating the metal from the flux.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

Patented a... 14, 1937 PRODUCTION OF REFINED MAGNESIUM AND MAGNESIUM ALLOYS Georg Schichtel, Radenthein, Austria, assignor to American Magnesium Metals Corporation, Pittsburgh, Pa., a corporation of Delaware No Drawing.
Application August 19, 1935, Se-
rial No. 36,853. In Austria March 30, 1933 5 Claims.
This invention relates to, the production of refined magnesium and magnesium alloys.
The present invention is a continuation in part of my application Serial No. 706,558, filed January 13, 1934 for the Production of refined magnesium and magnesium alloys, which has since become Patent No. 2,066,579, dated Jan. 5, 1937.
One object of the present invention is to provide a simple and commerciallypracticable process for the production-of compact metallic magnesium in a substantially chemically pure state.
Another object of 'my invention is to enable magnesium and magnesium alloys respectively, to be recovered, in a refined state, from waste, such as for example scrap arising from machine working and casting of magnesium or its alloys, and thereby not only to obtain a purer product as a result of my improved process, but also to ensure great saving by increasing the quantity of the recoveries.
The mechanical properties and resistance to corrosion of magnesium and its alloys are adversely aiiected by the presence of impurities,
especially extraneous oxides and other compounds (nitrides, carbides, silicides and the like), and also by other foreign substances such as carbon, even though said impurities be present in very small amounts.
The present invention aims at enabling magnesium being technically pure' (and its alloys) to be very extensively refined in thesimplest manner. The process is also admirably adapted for the elimination of impurities present during the recovery of magnesium by re-melting magnesium scrap (for example from machine working and from the foundry). Thus, for example in the case of magnesium dross, from which only 30% of the magnesium content could be recovered, as
refined metal, by treatment according to known processes, the present invention enables up to 90% of the metal originally present to be recovered as metal free from slag.
For this purpose, it was formerly the practice to re-melt magnesium scrap high in magnesium under a layer of chlorides, especially magnesium chloride. In such case, traces of magnesium chloride remained in the metal and had to be removed by special after-treatment. In order to to be melted at high temperatures, such as 800 C. and over, with small quantities of anhydrous magnesium chloride, corresponding approximately to the amount of I impurities present. Moreover, the use of saline melts consisting of mixture of magnesium chloride or carnallite (K Mg C13+6H20) with inspissating additions, such asoxides (e. g. of magnesium) or fluorides (of magnesium, calcium, aluminium or other metals) was proposed for the purpose. Subsequently it was proposed to replace these melts by potassium chloride, with additions of fluorspar, the salts primarily separating out during the cooling of the melt then serving as the thickening media.
This group cf.processes also includes the pro-' posal to refine magnesium by melting the metal in association with alkali chlorides (especially sodium chloride or potassium chloride) or mixtures of alkali chlorides, having melting points substantially higher than that of magnesium. These conditions are fulfilled by mixtures in which the sodium chloride or potassium chloride predominates. After melting, the 'whole is left to cool down to a temperature at which the salt, or saline mixture, has solidified to form a crust in which the impurities are occluded, whilst the metal is still fluid.
Another group of processes consists in refining the metal by melting it in association with additions which lead to the formation of an alloy to a moderate extent. specified as an addition of this kind in United States specification No, 1,698,647, with the qualification that, as an alloying component, this metal exerts a highly unfavorable influence on the magnesium- (page 1, lines 41 to 58). ,For this reason, the specification recommends that, when magnesium fluoride is used as the main Zinc, for example, is
refining agent, a small amount (0.05 to 0.3%) of metallic calcium should be incorporated.
According to the present. invention, the magnesium, or material containing same, that is to be refined is melted in association with small per cents by weight (referred to the total weightof material under treatment) being usually sufiicient.
The melting point of the selected salt or saline mixture should preferably be lower than that of. magnesium, but the specific gravity higher than that of the molten metal. If such salts be strewn over the metal during the melting down process, they melt sooner than the metal and envelop it, thereby protecting it against oxidation. This behavior has a specially advantageous eifect in the case of magnesium alloys, their melting points being lower than that of the metal. When the metal is stirred, with a further addition of the salts, after fusion has taken place, the higher specific gravity of thesaline melt causes it to subside quickly after absorption of the-impurities, so that, after settling, the refined metal can be poured off. Nevertheless the fused metal remains protected against oxidation by a supernatent thin film of the saline melt.
In order to obtain intimate mixing, it is advisable to melt the saline mixtures beforehand and to crush the melt for use.
Examples of appropriate salt mixtures are th (19) Sb13+30% EeCl3+ 30% ZnCl2+30% MgClz sb2s3+30% FeCla-l- 30% ZnCla+2 0% MgCl:
The mixtures numbered 8, 11, 18, 20 and 21 have proved in practice to be of particular efflcacy.
I use the term magnesium in the following claims to include not only crude or technically p'ure magnesium metal but also magnesium alloys and magnesium waste arising for example from machine working or casting of magnesium or its alloys.
I claim:-
1. The method of producing refined magnesium, which comprises melting impure magnesium with a fluid fluxcOntaining as purifying agents a mixture of antimony sulphide, chloride of iron, zinc chloride and magnesium chloride, agitating the molten metal with the flux, allowing the metal and the flux to segregate from eachother, and separating the metal from the flux.
2. The method of producing refined magnesium, which comprises melting impure magnesium with a fluid flux consisting of. 40 per cent of antimony trisulphide, 20 per cent of iron chloride, 10 per cent of zinc chloride and 30 per cent of. magnesium chloride, agitating the molten metal with the flux, allowing the metal and the 4. The method of refining magnesium, whichcomprises melting impure magnesium with a fluid flux containing as the main purifier a salt '25 flux to segregate from each other, and separat- ,of antimony selected from the group consisting of antimony selected from the group consisting of halides and sulfides, further containing a salt selected from the group of halides of cadmium, copper, zinc and magnesium. and further containing a halide of iron, agitating the molten metal with the flux, allowing the metal and the .flux to segregate from each other and separating the metal from the flux.
GEORG SCHICH'I'EL.
US36853A 1933-03-30 1935-08-19 Production of refined magnesium and magnesium alloys Expired - Lifetime US2101919A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448993A (en) * 1944-08-26 1948-09-07 Reconstruction Finance Corp Grain refining magnesium alloys
US2995439A (en) * 1959-02-02 1961-08-08 Union Carbide Corp Preparation of high purity chromium and other metals

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448993A (en) * 1944-08-26 1948-09-07 Reconstruction Finance Corp Grain refining magnesium alloys
US2995439A (en) * 1959-02-02 1961-08-08 Union Carbide Corp Preparation of high purity chromium and other metals

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