US1949082A - Method of obtaining heavy-metal beryllium alloys - Google Patents
Method of obtaining heavy-metal beryllium alloys Download PDFInfo
- Publication number
- US1949082A US1949082A US613270A US61327032A US1949082A US 1949082 A US1949082 A US 1949082A US 613270 A US613270 A US 613270A US 61327032 A US61327032 A US 61327032A US 1949082 A US1949082 A US 1949082A
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- US
- United States
- Prior art keywords
- beryllium
- magnesium
- metal
- alloy
- bath
- Prior art date
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- Expired - Lifetime
Links
- 229910001385 heavy metal Inorganic materials 0.000 title description 27
- 238000000034 method Methods 0.000 title description 15
- 229910000952 Be alloy Inorganic materials 0.000 title description 11
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 29
- 229910052790 beryllium Inorganic materials 0.000 description 24
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 21
- 229910052749 magnesium Inorganic materials 0.000 description 20
- 239000011777 magnesium Substances 0.000 description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 16
- 229910045601 alloy Inorganic materials 0.000 description 14
- 239000000956 alloy Substances 0.000 description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 229910052802 copper Inorganic materials 0.000 description 11
- 239000010949 copper Substances 0.000 description 11
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 9
- 150000001573 beryllium compounds Chemical class 0.000 description 9
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 229910052759 nickel Inorganic materials 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 229910000861 Mg alloy Inorganic materials 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- JZKFIPKXQBZXMW-UHFFFAOYSA-L beryllium difluoride Chemical compound F[Be]F JZKFIPKXQBZXMW-UHFFFAOYSA-L 0.000 description 4
- 229910001633 beryllium fluoride Inorganic materials 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000011872 intimate mixture Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 241000722270 Regulus Species 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- DMFGNRRURHSENX-UHFFFAOYSA-N beryllium copper Chemical compound [Be].[Cu] DMFGNRRURHSENX-UHFFFAOYSA-N 0.000 description 1
- ZMDCATBGKUUZHF-UHFFFAOYSA-N beryllium nickel Chemical compound [Be].[Ni] ZMDCATBGKUUZHF-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007514 turning Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
Definitions
- the present invention refers to a method of obtaining alloys of heavy metals, particularly of iron, copper, and nickel, with beryllium and is more especially concerned with a process in which beryllium compounds are reduced by the action of metals such as magnesium or magnesium alloys.
- An object of the present invention is to provide a method of producing beryllium alloys of the heavy metals which will enable the application of moderate working temperatures. such as are common in metallurgical operations, and the formation of such alloys without contamination by carbon and with the highest possible yield.
- a reducible compound of beryllium is introduced into a bath of molten heavy metal and therein brought into contact with a reducing agent such as magnesium or a magnesium alloy, the sensible heat of the heavy metal bath bringing about the reaction and ensuring the complete dissolution of the metallic beryllium formed in the heavy metal bath.
- a reducing agent such as magnesium or a magnesium alloy
- an intimate mixture of a finely divided reducible beryllium compound with magnesium or a magnesium alloy is introduced into the heavy metal bath, preferably in briquetted form.
- an alloy of magnesium containing between about 40 and percent,-and preferably about 50 percent, of aluminium is employed since the alloys within the range "indicated are extremely capable of reaction and are also easily reduced into pulverulent condition.
- alloys of beryllium with such heavy metals as are capable of forming alloys with magnesium (such as copper or nickel) are produced by preparing a molten alloy of magnesium and the heavy metal and stirring a reducible beryllium compound into the molten alloy.
- beryllium compound is reduced by the magnesium present in the bath and the beryllium metal thus formed passes over into the heavy metal, whereas the magnesium compound formed passes into the slag.
- beryllium oxide is employed as starting material, it is advantageous to add a flux which lowers the melting point of the magnesium oxide, so as to achieve a clear separation of the metal from the slag.
- the reducing metal is preferably applied in moderate excess, the latter largely being removed from the melt by evaporation at the temperatures of working.
- the magnesium applied in excess which largely remains in the bath owing to the comparatively low melting point of copper may be eliminated by heating the beryllium alloy obtained in the process up to about 1300 0.
- the temperature of the bath is raised to 1300 C., so as to eliminate the magnesium employed in excess, A copper-beryllium alloy containing about 7 percent of beryllium is obtained, the yield in metallic beryllium amounting to about 67 percent of the input.
- An iron-beryllium alloy is obtained containing 6.5 percent of beryllium, the yield in beryllium amounting to percent of the input.
- magnesium metal fllings into 200 parts by weight of molten nickel at a temperature of about 1550 C.
- a method or obtaining an alloy of heavy metals of the group consisting of copper, iron, and nickel withberyllium which comprises bringing a compound of beryllium from the group a bath of molten consisting of beryllium oxide and beryllium fluor- I ide into contact with magnesium within a bath oi molten heavy metal.
- a method of obtaining an alloy of heavy metals of thegroup consisting of copper, iron, and nickel with beryllium which comprises distributing an intimate mixture of finely divided magnesium and a compound of beryllium from the group consisting of beryllium oxide and beryllium fluoride in a bath of molten heavy metal.
- a method of obtaining an alloy of heavy metals of the group consisting of copper, iron, and nickel with beryllium which comprises distributing a briquetted mixture of flnely divided magnesium and a compound or beryllium from the group consisting of beryllium oxide and beryllium fluoridein a bath of molten heavy metal.
- a method of obtaining an alloy of heavy metals of the group consisting of copper and nickel with beryllium which comprises introducing a compound of beryllium from'the group consisting of beryllium oxide and beryllium fluoride into a ba h of molten heavy metal containing, in the form of .an alloy, sufficient magnesium to effect reduction of said beryllium compound.
- a method of obtaining a copper-beryllium alloy which comprises brin i a compound of beryllium from the group consisting of beryllium oxide and beryllium fluoride into contact with a quantity of magnesium somewhat in excess over that required for reducing said beryllium compound within a bath of molten heavy metal and,
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Feb. 27, 1934 PATENT oFFlc METHOD OF OBTAINING HEAVY-METAL. BERYLLIUM ALLOYS Ernst Pokorny, Leipzig, Germany, assignor to Farbenindustrie Aktiengesellschaft,
Frankfort-on-the-Main, Germany No Drawing. Application May 24, 1932, Serial No. 613,270. In Germany May 28, 1931 6 Claims.
The present invention refers to a method of obtaining alloys of heavy metals, particularly of iron, copper, and nickel, with beryllium and is more especially concerned with a process in which beryllium compounds are reduced by the action of metals such as magnesium or magnesium alloys.
Hitherto the manufacture of heavy-metal beryllium alloys was usually carried out by introducing electrolytically obtained pure beryllium metal into a bath of molten heavy metal. The necessity of first having to produce pure beryllium, however, renders this process uneconomical. The same pertains in regard to another proposal which contemplates the electrolytic deposition, in combination, of the components of the alloy.
Another group of processes for the formation of heavy-metal beryllium alloys is based on the reduction of mixtures of beryllium compounds with reducible heavy metal compounds by the action of carbon, these processes yielding products containing carbon. The same disadvantage is associated with the suggested employment of carbides of the alkaline earth metals as reducing agents, and is further aggravated by the fact that the reduction, because of the diificult fusibility of the carbides, requires temperatures of. at least about 1800 C. All these processes are further.
characterized by low yields in beryllium.
It has further been suggested to produce carban-free beryllium metal by reducing beryllium compounds by means of aluminium, calcium or magnesium. In this manner a mixture of metal and oxides is invariably obtained, and the separation of the metal causes grave difficulties when working on an industrial scale. In order to obtain a satisfying yield of carbon-free heavy-metal beryllium alloys it is also possible to cause mix- .tures of magnesium or magnesium alloys with a heavy metal to react upon reducible beryllium compounds. However, the temperatures required for obtaining the metal in the form oi. a regulus are far above 2000 C.
An object of the present invention, therefore. is to provide a method of producing beryllium alloys of the heavy metals which will enable the application of moderate working temperatures. such as are common in metallurgical operations, and the formation of such alloys without contamination by carbon and with the highest possible yield.
. To this end, according to the present invention, a reducible compound of beryllium is introduced into a bath of molten heavy metal and therein brought into contact with a reducing agent such as magnesium or a magnesium alloy, the sensible heat of the heavy metal bath bringing about the reaction and ensuring the complete dissolution of the metallic beryllium formed in the heavy metal bath.
According to one modification of the invention, an intimate mixture of a finely divided reducible beryllium compound with magnesium or a magnesium alloy is introduced into the heavy metal bath, preferably in briquetted form. Advantageously an alloy of magnesium containing between about 40 and percent,-and preferably about 50 percent, of aluminium is employed since the alloys within the range "indicated are extremely capable of reaction and are also easily reduced into pulverulent condition.
.According to another modification of the invention alloys of beryllium with such heavy metals as are capable of forming alloys with magnesium (such as copper or nickel) are produced by preparing a molten alloy of magnesium and the heavy metal and stirring a reducible beryllium compound into the molten alloy. The
beryllium compound is reduced by the magnesium present in the bath and the beryllium metal thus formed passes over into the heavy metal, whereas the magnesium compound formed passes into the slag. When beryllium oxide is employed as starting material, it is advantageous to add a flux which lowers the melting point of the magnesium oxide, so as to achieve a clear separation of the metal from the slag.
The reducing metal is preferably applied in moderate excess, the latter largely being removed from the melt by evaporation at the temperatures of working. When making copper-beryllium alloys according to the present invention, the magnesium applied in excess which largely remains in the bath owing to the comparatively low melting point of copper may be eliminated by heating the beryllium alloy obtained in the process up to about 1300 0.
Examples 1) 150 parts by weight of beryllium oxide are intimately mixed with 160 parts by weight of filings or turnings of magnesium and made into briquettes of about 1 to 10 cubic inches size. The latter are immersed in a bath of 400 parts by weight of molten copper at between about 1100 to 1200 C. under a hydrogen atmosphere while stirring. An overheating of the bath should be avoided. On attaining the reaction temperature, the reaction which is exothermic rapidly pervades the whole mass and the beryllium metal tormed further vigorousstirring. The magnesium oxide produced by. the reaction floats on the surface of the melt and protects the beryllium metal from" oxidation. After the reaction is completed the temperature of the bath is raised to 1300 C., so as to eliminate the magnesium employed in excess, A copper-beryllium alloy containing about 7 percent of beryllium is obtained, the yield in metallic beryllium amounting to about 67 percent of the input.
(2) 100 parts by weight of an alloy consisting of percent of magnesium and '75 percent of copper are molten and parts by weight of beryllium oxide stirred thereinto. When the reaction is completed the temperature of the bath is raised to 1400 C. so as to evaporate the magnesium applied in excess. A beryllium copper alloy containing 5.7 percent of beryllium is obtained, the yield amountingto 52.8 percent.
(3) A mixture of 100 parts by weight or beryllium oxide and 100 parts by weight of an alloy containing about equal parts by weight of magnesium and aluminium, in form' of filings, is formed into briquettes of about 1 to 10 cubic inches size by applying a high pressure and the briquettes are introduced while stirring into 500 parts by weight of molten iron at about 1600 C An iron-beryllium alloy is obtained containing 6.5 percent of beryllium, the yield in beryllium amounting to percent of the input.
- (4) In the same manner, a beryllium-nickel alloy containing about 9.5 percent of beryllium with a yield in beryllium of 70 percent is obtained by introducing a mixture of 100 parts by weight of beryllium fluoride and 100 parts by weight 0:!
magnesium metal fllings into 200 parts by weight of molten nickel at a temperature of about 1550 C.
Iclaim:- l. A method of obtaining an alloy of heavy metals of the group consisting of copper, iron,
- and nickel with beryllium, which comprises bringing a reducible compound of beryllium into conalloys with the copper, this being promoted by tact with magnesium within heavy metal. 5
2. A method or obtaining an alloy of heavy metals of the group consisting of copper, iron, and nickel withberyllium, which comprises bringing a compound of beryllium from the group a bath of molten consisting of beryllium oxide and beryllium fluor- I ide into contact with magnesium within a bath oi molten heavy metal.
3. A method of obtaining an alloy of heavy metals of thegroup consisting of copper, iron, and nickel with beryllium, which comprises distributing an intimate mixture of finely divided magnesium and a compound of beryllium from the group consisting of beryllium oxide and beryllium fluoride in a bath of molten heavy metal.
4. A method of obtaining an alloy of heavy metals of the group consisting of copper, iron, and nickel with beryllium, which comprises distributing a briquetted mixture of flnely divided magnesium and a compound or beryllium from the group consisting of beryllium oxide and beryllium fluoridein a bath of molten heavy metal.
5. A method of obtaining an alloy of heavy metals of the group consisting of copper and nickel with beryllium, which comprises introducing a compound of beryllium from'the group consisting of beryllium oxide and beryllium fluoride into a ba h of molten heavy metal containing, in the form of .an alloy, sufficient magnesium to effect reduction of said beryllium compound. 6. A method of obtaining a copper-beryllium alloy, which comprises brin i a compound of beryllium from the group consisting of beryllium oxide and beryllium fluoride into contact with a quantity of magnesium somewhat in excess over that required for reducing said beryllium compound within a bath of molten heavy metal and,
when the reaction is completed, raising the temperature of the metal bath so as to evaporate .the magnesium in excess.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1949082X | 1931-05-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1949082A true US1949082A (en) | 1934-02-27 |
Family
ID=7750886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US613270A Expired - Lifetime US1949082A (en) | 1931-05-28 | 1932-05-24 | Method of obtaining heavy-metal beryllium alloys |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1949082A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE766603C (en) * | 1934-10-23 | 1953-07-06 | Calloy Ltd | Process for the reduction of oxides of the alkaline earth metals |
-
1932
- 1932-05-24 US US613270A patent/US1949082A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE766603C (en) * | 1934-10-23 | 1953-07-06 | Calloy Ltd | Process for the reduction of oxides of the alkaline earth metals |
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