US854018A - Process of reducing metallic oxids. - Google Patents
Process of reducing metallic oxids. Download PDFInfo
- Publication number
- US854018A US854018A US27985705A US1905279857A US854018A US 854018 A US854018 A US 854018A US 27985705 A US27985705 A US 27985705A US 1905279857 A US1905279857 A US 1905279857A US 854018 A US854018 A US 854018A
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- US
- United States
- Prior art keywords
- silicon
- oxid
- metallic
- oxids
- reducing
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 title description 14
- 230000001603 reducing effect Effects 0.000 title description 11
- 230000008569 process Effects 0.000 title description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 59
- 239000010703 silicon Substances 0.000 description 59
- 229910052710 silicon Inorganic materials 0.000 description 59
- 229910052751 metal Inorganic materials 0.000 description 20
- 239000002184 metal Substances 0.000 description 20
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- 230000004907 flux Effects 0.000 description 11
- 239000011651 chromium Substances 0.000 description 10
- 150000002739 metals Chemical class 0.000 description 10
- 229910045601 alloy Inorganic materials 0.000 description 9
- 239000000956 alloy Substances 0.000 description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 8
- 229910052804 chromium Inorganic materials 0.000 description 8
- 229910052742 iron Inorganic materials 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 229910000604 Ferrochrome Inorganic materials 0.000 description 3
- 238000003723 Smelting Methods 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229940124024 weight reducing agent Drugs 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 229910021332 silicide Inorganic materials 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- XDXHAEQXIBQUEZ-UHFFFAOYSA-N Ropinirole hydrochloride Chemical compound Cl.CCCN(CCC)CCC1=CC=CC2=C1CC(=O)N2 XDXHAEQXIBQUEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- ZXOKVTWPEIAYAB-UHFFFAOYSA-N dioxido(oxo)tungsten Chemical compound [O-][W]([O-])=O ZXOKVTWPEIAYAB-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- SBEQWOXEGHQIMW-UHFFFAOYSA-N silicon Chemical compound [Si].[Si] SBEQWOXEGHQIMW-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
Definitions
- FREDERICK M BECKET, OF NIAGARA FALLS, NEW YORK, SSIGNOR TO ELECTRO METALLURGICAL COMPANY, A CORPORATION OF EST VIR- GINIA.
- his invention is a process for the production of metals and alloys of low silicon and carbon content, and is more particularly applicable to the metals chromium, tungsten, molybdenum and vanadium and to the alloys of these metals with iron or nickel.
- the invention consists in reducing a suitable oxid or oxygen-containing compound or mixture of oxids by silicon, the silicon being used in proportions and under conditions to insure a low silicon content of the product.
- the conditions necessary for substantially complete reduction of the refractory metallic oxid or oxids above mentioned and the prod uction of metals or alloys of low silicon and carbon content are obtainable so far as known only in an electric furnace.
- a basic flux is used to combine with the silica derived from the oxidation of the silicon.
- Metallurgists have long been familiar with the reducing action of silicon on certain metallic oxids, such as oxid of iron, and advantage is taken of this chemical reaction in many industries,-for example in the manu facture of steel.
- silicon exists in the form-of an alloy, its reducing properties are employed as a means of eliminating it from the finished product rather than as a means of producing further quantities of metal, and the proportion of reducible oxid used for its remo'val is largely in excess of that theoretically i'iecessary.
- silicon is employed to reduce metallic oxids dissolved in molten metals, and in this form it is also used or the production of double silicides of the metals, and of alloys containing considerable .-ropor tions of silicon.
- metallic silicon has not been considered an article of commerce. The metal is now produced in the electric furnace, often associated with considerable quantities of iron, at such cost and in such quantity as to permit its economical application as a reduc ing agent in certain electro-metallurgical operations.
- silicon although not so I electropositive as aluminium, may be advantageously employed in the electric furnace as a reducing agent in the production of chromium, molybdenum, tungsten and vanadium, or the iron or nickel alloys of these metals.
- a suitable mixture consisting of silicon, an oxid of one or more of the above metals, and a basic flux is treated in an elec tric'fur'nace, the advantages of a continuous and very rapid process may be obtained, and by suitably proportioning the ingredients of the charge the silicon content in the reduced metals maybe made as smallas 0.01 percent. or less.
- a fair commercial grade of chromite contains 52 percent. Cr,(), and 16 percent. FeO, and 100 pounds of this ore will therefore require, according to the above reactions, 17.7 pounds silicon for complete reduction of the chromium and iron.
- Arepresentative analy sis of ferrochromium made by this method is as follows: Chromium 71.00 percent; iron 28.40 percent; carbon 0.50 percent; silicon 0.10 percent.
- the silicon in a fairly fine state of division and the metal is generally crushed so that it will all pass a ten-mesh screen.
- the state of division of the silicon depends on the scale of the operation.
- the use of a basic flux in the production of ferrochromium is not essential although advantageous.
- Most commercial chromites contain from S to 15 percent. A1 0 and 8 to 15 percent. MgO. These materials serve as basic flux for the silica present in the ore and for that produced by oxidation of the silicon; but the proportions are such that to maintain this slag fluid for tapping, a higher temperature is necessary than that required for complete reduction of the chromium and iron oxids by silicon.
- chromium and iron may be obtained from the ore used and the alloy contains only fractions of a percent. of carbon and silicon. It is not essential that the proportions be precisely those indicated by theory, because in the casein which very low silicon content is required in the alloy, (less than 0.2 percent.), the chromite is used in very slight excess of the theroetical proportions; and in the case in which a silicon content as high as one percent. may be permitted, the silicon is used in very slight excessf There'is slight advantage in the latter method on account of the fact that the yield of metal from the ore is slightly higher. In both cases, however, the variations from the theoretical proportions are small and the yields high.
- the electric furnace operation may be earriedout by fusing the ore and flux and-then adding thereto the metallic silicon, or by fusing a mixture of ore and silicon and adding flux to this bath from time to time, but I have not found these methods to be as eflicient as that above described. 7
- Thc'use of silicon as a reducing .agent is highly advantageous in practice as compared with the use ofaluminium for several reasons among which may be mentioned the relatively large weight of metal which is separated per unit weight of the reducing agent the comparative ease'yvith which silicon is obtained a fine state of division whereby a more intimate mixture is obtainable; the fact that with such mixtures the reaction proceeds more quietl'y and' wi thless loss of material; and more particularlybecause silicious ores, which are relatively inexpensive, may be successfully used.
- Aluminium reduces silicon from the silica in- It is possible to melt variably present in such ores as chromite, wolframite, etc., and I have found in practice that silicon so reduced, as well as portions of the aluminium fused for reduction, alloy with the reduced metal, thereby necessitating either a costly selection of ores or other expensive method in case a product low in silicon is required. Furthermore in such case there is liability to the introduction of both silicon and aluminium into the metal, and in practice it is found to be more difficult to eliminate small percentages of the latter metal than of the former.
- reaction not being of a self-propagating character.
- I claim 1 The process of reducing refractory metallic oxids which consists in smelting a charge containing a metallic oxid reducible by silicon and silicon, the silicon being present in substantially the proportion required to combine with the oxygen of said oxid whereby a substantially complete oxidation of the silicon is secured and a product low in' silicon is obtained, substantially as described.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
UNITED STATES.
PATENT orinon.
FREDERICK M. BECKET, OF NIAGARA FALLS, NEW YORK, SSIGNOR TO ELECTRO METALLURGICAL COMPANY, A CORPORATION OF EST VIR- GINIA.
PROCESS OF REDUCING METALLIC OXIDS;
Specification of Letters Patent.
Patented May 21, 1907.
Application filed se tember 23, 1905- Serial No. 279,857.
To all 1072,0711, it may concern- Be t known that I, FREDERICK M. BECKET,
"a subject of the King of Great Britain, residing at Niagara Falls, in the county of Niagara and State of New York, have invented certain new and useful Improvements in Processes of Reducing Metallic Oxids, of which the following is a specification.
his invention is a process for the production of metals and alloys of low silicon and carbon content, and is more particularly applicable to the metals chromium, tungsten, molybdenum and vanadium and to the alloys of these metals with iron or nickel.
The invention consists in reducing a suitable oxid or oxygen-containing compound or mixture of oxids by silicon, the silicon being used in proportions and under conditions to insure a low silicon content of the product. The conditions necessary for substantially complete reduction of the refractory metallic oxid or oxids above mentioned and the prod uction of metals or alloys of low silicon and carbon content are obtainable so far as known only in an electric furnace. Preferably a basic flux is used to combine with the silica derived from the oxidation of the silicon.
Metallurgists have long been familiar with the reducing action of silicon on certain metallic oxids, such as oxid of iron, and advantage is taken of this chemical reaction in many industries,-for example in the manu facture of steel. In these cases the silicon exists in the form-of an alloy, its reducing properties are employed as a means of eliminating it from the finished product rather than as a means of producing further quantities of metal, and the proportion of reducible oxid used for its remo'val is largely in excess of that theoretically i'iecessary. In the form of metallic silicides, silicon is employed to reduce metallic oxids dissolved in molten metals, and in this form it is also used or the production of double silicides of the metals, and of alloys containing considerable .-ropor tions of silicon. Until a comparatively recent date metallic silicon has not been considered an article of commerce. The metal is now produced in the electric furnace, often associated with considerable quantities of iron, at such cost and in such quantity as to permit its economical application as a reduc ing agent in certain electro-metallurgical operations.
l I have found that silicon, although not so I electropositive as aluminium, may be advantageously employed in the electric furnace as a reducing agent in the production of chromium, molybdenum, tungsten and vanadium, or the iron or nickel alloys of these metals. When a suitable mixture consisting of silicon, an oxid of one or more of the above metals, and a basic flux is treated in an elec tric'fur'nace, the advantages of a continuous and very rapid process may be obtained, and by suitably proportioning the ingredients of the charge the silicon content in the reduced metals maybe made as smallas 0.01 percent. or less.
As a specific example of the process I will describe its application to the mamifacture of low carbon and low silicon ferrochromium from chromite. As the chromium in chromite exists as chromium sesquioxid, Cr O,, and practically all the iron as ferrous oxid, FeO; the following reactions take place.
A fair commercial grade of chromite contains 52 percent. Cr,(), and 16 percent. FeO, and 100 pounds of this ore will therefore require, according to the above reactions, 17.7 pounds silicon for complete reduction of the chromium and iron. Arepresentative analy sis of ferrochromium made by this method is as follows: Chromium 71.00 percent; iron 28.40 percent; carbon 0.50 percent; silicon 0.10 percent.
It is advantageous to use the silicon in a fairly fine state of division and the metal is generally crushed so that it will all pass a ten-mesh screen. However, the state of division of the silicon depends on the scale of the operation. The use of a basic flux in the production of ferrochromium is not essential although advantageous. Most commercial chromites contain from S to 15 percent. A1 0 and 8 to 15 percent. MgO. These materials serve as basic flux for the silica present in the ore and for that produced by oxidation of the silicon; but the proportions are such that to maintain this slag fluid for tapping, a higher temperature is necessary than that required for complete reduction of the chromium and iron oxids by silicon.
By mixing chromite and silicon in practil cally theoretical proportions, together with withdrawn as desired.
some basic flux such as lime, and bringing the mixture to a stateof fusion in an electric furnace, a very high yield of chromium and iron may be obtained from the ore used and the alloy contains only fractions of a percent. of carbon and silicon. It is not essential that the proportions be precisely those indicated by theory, because in the casein which very low silicon content is required in the alloy, (less than 0.2 percent.), the chromite is used in very slight excess of the theroetical proportions; and in the case in which a silicon content as high as one percent. may be permitted, the silicon is used in very slight excessf There'is slight advantage in the latter method on account of the fact that the yield of metal from the ore is slightly higher. In both cases, however, the variations from the theoretical proportions are small and the yields high.
I do not limit myself to any particular type of electric furnace but I have found it advantageous to carry on the reduction continuously in an electric furnace in which the' current passes through, a molten bath of a mixture of ore, silicon and flux, and from whlch part or all of the metal or slag may be a mixture of silicon and oxid or oxygen containing compound of the metals referred to and not effect complete reduction; and to obtain a high yield of the desired metal or alloy and to insure a low silicon content therein, I have found it advantageous to feed the mixture to a bath which is constantly maintained at a temperature higher than that necessary to cause some reaction.
The electric furnace operation may be earriedout by fusing the ore and flux and-then adding thereto the metallic silicon, or by fusing a mixture of ore and silicon and adding flux to this bath from time to time, but I have not found these methods to be as eflicient as that above described. 7
As the reaction betweensilicon and the above mentioned metallic oxids is strongly exothermic, a relatively small amount of electrical energyis requi dfor the reduction; moreover the react on: 'i'oceeds without evolution of gas whieh 'i'is i great practical advantage. Thc'use of silicon as a reducing .agent is highly advantageous in practice as compared with the use ofaluminium for several reasons among which may be mentioned the relatively large weight of metal which is separated per unit weight of the reducing agent the comparative ease'yvith which silicon is obtained a fine state of division whereby a more intimate mixture is obtainable; the fact that with such mixtures the reaction proceeds more quietl'y and' wi thless loss of material; and more particularlybecause silicious ores, which are relatively inexpensive, may be successfully used. Aluminium reduces silicon from the silica in- It is possible to melt variably present in such ores as chromite, wolframite, etc., and I have found in practice that silicon so reduced, as well as portions of the aluminium fused for reduction, alloy with the reduced metal, thereby necessitating either a costly selection of ores or other expensive method in case a product low in silicon is required. Furthermore in such case there is liability to the introduction of both silicon and aluminium into the metal, and in practice it is found to be more difficult to eliminate small percentages of the latter metal than of the former.
the reaction not being of a self-propagating character.
I claim 1. The process of reducing refractory metallic oxids which consists in smelting a charge containing a metallic oxid reducible by silicon and silicon, the silicon being present in substantially the proportion required to combine with the oxygen of said oxid whereby a substantially complete oxidation of the silicon is secured and a product low in' silicon is obtained, substantially as described.
2. The process of reducing metallic oxids which consists in electrically smelting acharge containing a metallic oxid reducible by silicon and silicon, the silicon being present in substantially the proportion required to combine with the oxygen of said oxid whereby a substantially complete oxidation of the silicon is secured and a product low in silicon is obtained, substantially as described.
3. The process of reducing refractory metallic oxids which consists in smelting a charge containing a metallic oxid reducible by silicon, silicon and a basic flux, the silicon being present in substantially the proportion required to combine with the oxygen of said oxid whereby a product low in silicon is oboxid whereby a product low in silicon is ob'.
tained, substantially as described.
5. The process of reducing metallic oxids which consists in passing an electric current through a molten bath containing a metallic oxid reducible by silicon and silicon, the silicon being present in substantially the proportion required to combine with the oxygen of said oxid whereby a product low in silicon is obtained, substantially as described.
6. The process of reducing metallic oxids which consists in passing an electric current 10 inn a metallic oxid,
through a molten ba'thcontaining a metallic oxid, reducible by silicon silicon and a basic flux, the silicon being present in substantially the proportion required to combine with the oxygen of said oxid whereby a product low in silicon 1s obtained, substantially as described.
7. The continuous process of reducingme- 1 tallic oxlds which consists in passing an eleca molten bath containtric current through reducible by silicon s1h con and a basic flux, adding fresh portions of the charge and Withdrawing the products as required, substantially as described.
In testimony whereof, I afiix my signature in presence of two witnesses.
FREDERICK M. BECKET.
\Vitnesses:
J AS. H. "IIITING, WM. L. IIEIM.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27985705A US854018A (en) | 1905-09-23 | 1905-09-23 | Process of reducing metallic oxids. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27985705A US854018A (en) | 1905-09-23 | 1905-09-23 | Process of reducing metallic oxids. |
Publications (1)
Publication Number | Publication Date |
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US854018A true US854018A (en) | 1907-05-21 |
Family
ID=2922475
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US27985705A Expired - Lifetime US854018A (en) | 1905-09-23 | 1905-09-23 | Process of reducing metallic oxids. |
Country Status (1)
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE749749C (en) * | 1939-04-23 | 1944-12-05 | Process for the production of metals and alloys | |
US2905551A (en) * | 1954-12-24 | 1959-09-22 | Lonza Electric & Chem Works | Manufacturing of metallic uranium |
US2907651A (en) * | 1954-09-21 | 1959-10-06 | Reading Anthracite Company | Process for the economic utilization of waste carbonaceous material of fuel ashes, and the resulting products |
-
1905
- 1905-09-23 US US27985705A patent/US854018A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE749749C (en) * | 1939-04-23 | 1944-12-05 | Process for the production of metals and alloys | |
US2907651A (en) * | 1954-09-21 | 1959-10-06 | Reading Anthracite Company | Process for the economic utilization of waste carbonaceous material of fuel ashes, and the resulting products |
US2905551A (en) * | 1954-12-24 | 1959-09-22 | Lonza Electric & Chem Works | Manufacturing of metallic uranium |
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