US476914A - Myrthil bernard and ernest bernard - Google Patents
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- US476914A US476914A US476914DA US476914A US 476914 A US476914 A US 476914A US 476914D A US476914D A US 476914DA US 476914 A US476914 A US 476914A
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- Prior art keywords
- aluminium
- vessel
- bath
- bernard
- cathode
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- 239000004411 aluminium Substances 0.000 description 88
- 229910052782 aluminium Inorganic materials 0.000 description 88
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 88
- 229910052751 metal Inorganic materials 0.000 description 34
- 239000002184 metal Substances 0.000 description 34
- 229910045601 alloy Inorganic materials 0.000 description 22
- 239000000956 alloy Substances 0.000 description 22
- 238000000034 method Methods 0.000 description 18
- 229910000838 Al alloy Inorganic materials 0.000 description 16
- KRHYYFGTRYWZRS-UHFFFAOYSA-M fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 16
- 238000005868 electrolysis reaction Methods 0.000 description 14
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 14
- 229910052708 sodium Inorganic materials 0.000 description 14
- 239000011734 sodium Substances 0.000 description 14
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical class [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 12
- REHXRBDMVPYGJX-UHFFFAOYSA-H Sodium hexafluoroaluminate Chemical compound [Na+].[Na+].[Na+].F[Al-3](F)(F)(F)(F)F REHXRBDMVPYGJX-UHFFFAOYSA-H 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 10
- 229910001610 cryolite Inorganic materials 0.000 description 10
- 239000004020 conductor Substances 0.000 description 8
- 150000002222 fluorine compounds Chemical class 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 239000011449 brick Substances 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 229910052570 clay Inorganic materials 0.000 description 4
- 231100000078 corrosive Toxicity 0.000 description 4
- 231100001010 corrosive Toxicity 0.000 description 4
- 230000004907 flux Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 230000000630 rising Effects 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 241001676573 Minium Species 0.000 description 2
- 229910001295 No alloy Inorganic materials 0.000 description 2
- 241000282890 Sus Species 0.000 description 2
- 150000001399 aluminium compounds Chemical class 0.000 description 2
- 229940077746 antacids containing aluminium compounds Drugs 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 230000002452 interceptive Effects 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 230000036633 rest Effects 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
- C25C3/36—Alloys obtained by cathodic reduction of all their ions
Definitions
- Our invention has reference to improvements in the process of and apparatus for producing aluminium or aluminium alloys by electrolysis.
- the vessel or crucible containing the bath was either made entirely of or lined with metal to prevent the silicates in the body of ordinary crucibles from combining with the aluminium or aluminium al- 10y, since such combination renders the product brittle.
- metallic or metallined crucible was used, the same was sometimes utilized as the cathode, so that the product obtained was an alloy of aluminium with the metal of the containing-vessel.
- the electrolytic bath is specifically heavier than aluminium, so that thelatter or its alloys risesto the surface of the bath, results in the burning of a portion of the product upon contact with the air at a very high temperature.
- This rising of the product to the surface is also a great inconvenience, since it requires constant attention and manipulation for removing the liberated aluminium or aluminium alloy, which interferes with the feeding of the baththat is to say, since from time to time the bath has to be replenished by the addition of cryolite and its flux, which are piled upon the surface of the bath, the removal of the aluminium which has risen to the surface becomes difficult.
- our invention comprises the use of an electrolytic bath which is specifically lighter than aluminium or its alloys, so that as either of them is liberated it sinks to the bottom of the crucible and may be drained off without exposure to the air for any considerable time at the high temperature which ithas when risen to the surfaceandwithout interfering with the feeding of the bath, so that the process maybe continued for a very long time withoutsensible interruption.
- Figure 1 represents a vertical section of an, electrolytic apparatus constructed in accordance with our invention for the production ofaluminium alloys
- Fig. 2 is a like view of. the apparatus as modified for the production the product desired. If it is desired to obtain of pure aluminium.
- cryo-f lite As above stated, we may use artificial cryo-f lite, and in so doing we are not obliged toadhere to the proportions of fluoride of alu-. minium and fluoride of sodium as found in Thus, for instance, we may native cryolite.
- Fluoride of aluminium 35 Fluoride of sodium 10 Chloride of sodium 55 Total 100 .
- One of these characteristics is its great fluid-i ity, whereby the bath behaves under the ac- ⁇ tion of the current with the same regularityi as a salt in solution, and thatattemperaturesi varying from 900 to 1,100 centigrade, which are the highest temperatures used by us;
- the second of these characteristics is that the; bath is very little volatile, so that not more thanabout five per cent. of the whole mass is lost in twenty-four hours.
- a containing vessel or crucible I made of the, metal with which the alloy with aluminium is; It may therefore be made of any of the base metals which readily alloy, with aluminium and which at the same time are refractory at the temperatures at which;
- This containing vessel or crucible is embedded in fire bricks or clay c: in such a manner that the flame of the fur-Q nace does not directly impinge upon the ves-Q sel, and it is formed with an inclined bottom, as shown, for a purpose which will presently is drained off by opening the orifice T.
- Electrodes A A are sus' pended within the bath and are used as anodes, while the containing-vessel 18 used or may be used as the cathode, so that the current, entering by the electrodes A A, traverses the bath and issues by a conductor connected with the containing-vessel, all as indicated by the arrows in the drawings.
- the anodes may be made of dilterent materials, according to aluminium moderately alloyed with the metal the anodes will be made of carbon.
- the electrolytic bath being made, as above described, specifically lighterthan aluminium, the alloy (1, formed by the use of the apparatus represented in Fig. 1,will flow down along the sides of the containing-Vessel and will accumulate upon the inclined bottom, and after a suitable quantity has thus accumulated hit e time when this is done-that is to say, the time when a sufficient quantity of the deposited metal has accumulated-is easily learned by experience, and may, in fact, be predetermined with great accuracy by computation, since, as above stated, our electrolytic bath behaves with the same regularityas a salt in solution. Knowing, therefore, the volume and electro-motive force of the current employed; knowing, also, the electrical resistance of the bath and the counter electro-motive force of the same, the amount of metal liberated within a certain time can be accurately computed.
- Fig. .2 For the production of pure aluminium an apparatus like that represented in Fig. .2is used. It consists of .the-containing-vessel l), which in this case has a horizontal bottom and is embedded in fire bricks or clay 0, substantially like the apparatus described with reference to Fig. 1.
- both the anode and the cathode are made of carbon.
- the process of producing aluminium by electrolysis which consists in first making a molten bath containing fluoride of aluminium and then passing the main portion of an electric current through the bath between electrodes immersed in the bath and the remaining fraction of the current between the anode and the containing-vessel, substantially as described.
- the process of producing aluminium by electrolysis which consists in first making a melted bath which is specifically lighter than aluminium and which contains fluoride of aluminium and chloride of sodium and then passing the main portion of an electric current through the bath between suitable electrodes placed in the bath and the remaining fraction of the current through the anode, the bath, and containing-vessel, substantially as described.
- the process of producing aluminium by electrolysis which consists in melting together cryolite and chloride of sodium in such proportions as to form a bath which is specifically lighterthan aluminium and then passing the main portion of an electric current through the bath between an anode and a cathode to the exclusion of the containing-vessel and the remaining fraction of the current through the bath between the anode and the containing-vessel as a fractional cathode, whereby pure aluminium is liberated at the cathode and aluminium alloy is formed upon the containing-vessel, substantially as described.
- An apparatus for producing aluminium by electrolysis consisting of a metallic contaming-vessel or crucible for the bath, an anode, a cathode, a depositing-vessel or crucible for the same located within and insulated from the containing-vessel, and a branch conductor of high electrical resistance between the cathode and the containing-vessel, whereby the latter becomes a fractional cathode, substantially as described.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Metals (AREA)
Description
(No Model.)
M. 85 E. BERNARD.
PROOESS OF AND APPARATUS FOR THE EXTRACTION 0F ALUMINIUM.
Patented June 14, 1892.
Jgl
1': News PEYERS co., Puo'ro-umm, WASHINGTON, n. c.
UNITED STATES PATENT OFFICE.
MYRTHIL BERNARD AND ERNEST BERNARD, OF PARIS, FRANCE.
PROCESS OF AND APPARATUS FOR THE EXTRACTION OF ALUMINIUM.
SPECIFICATION forming part of Letters Patent No. 476,914, dated June 14, 1892.
Application filed January 20, 1888. Serial No. 261,378. (No model.) Patented in France May 17, 1887,1T0. 183,691 in Belgium July 14,1887,No. 78,208: in Luxemburg July 14,1887, No. 862, and in England July 18,1887,N0.10,057.
To all whom it may concern.-
Bet it known that we, MYRTHIL BERNARD and ERNEST BERNARD, citizens of the Republic of France, and residents of Paris, in the Republicof France, have invented certain new and useful Improvements in the Process of and Apparatus for the Extraction ofAluminium from its Fluorides by Electrolysis, (for which I have obtained patents in- France May 17, 1887, No. 183,691; in Belgium July 14,, 1887, No. 78,208; in Luxemburg July 14, 1887, No. 862, and in Great Britain July 18, 1887, No. 10,057,) of which the following is a specification.
Our invention has reference to improvements in the process of and apparatus for producing aluminium or aluminium alloys by electrolysis.
In the production of aluminium by electrolysis as heretofore practiced fluoride of aluminium has been melted with a suitable flux and has then been electrolyzed, whereby the aluminium was liberated at the cathode, and either combining with the latter, when of metal, and thus forming an alloy of aluminium with that metal, or rising along the face of the cathode to the surface of the bath, from which it had to be removed. This latter was the case when the cathode Was non-metallic and usually of carbon or when it was made of a metal that could form no alloy with aluminium. In some cases the vessel or crucible containing the bath was either made entirely of or lined with metal to prevent the silicates in the body of ordinary crucibles from combining with the aluminium or aluminium al- 10y, since such combination renders the product brittle. When such metallic or metallined crucible was used, the same was sometimes utilized as the cathode, so that the product obtained was an alloy of aluminium with the metal of the containing-vessel.
In the processes so far described there are several inconveniences and defects which render the production of aluminium or aluminium alloy upon a large scale very expensive and unsatisfactory. In the first place,
the fact that the electrolytic bath is specifically heavier than aluminium, so that thelatter or its alloys risesto the surface of the bath, results in the burning of a portion of the product upon contact with the air at a very high temperature. This rising of the product to the surface is also a great inconvenience, since it requires constant attention and manipulation for removing the liberated aluminium or aluminium alloy, which interferes with the feeding of the baththat is to say, since from time to time the bath has to be replenished by the addition of cryolite and its flux, which are piled upon the surface of the bath, the removal of the aluminium which has risen to the surface becomes difficult. \Vith a view of avoiding this difficulty our invention comprises the use of an electrolytic bath which is specifically lighter than aluminium or its alloys, so that as either of them is liberated it sinks to the bottom of the crucible and may be drained off without exposure to the air for any considerable time at the high temperature which ithas when risen to the surfaceandwithout interfering with the feeding of the bath, so that the process maybe continued for a very long time withoutsensible interruption. In the second place, when a metallic crucible was used as the cathode, whereby the crucible is consumed in the process and becomes an element of the product, pure aluminium could not be produced; but when it was attempted to produce pure aluminium by using a metallic crucible without making it the cathode itwas found that the melted fluorides acted so corrosively upon the metal of the crucible that it soon became destroyed and in a measure combined with the aluminium, forming impure alloys where pure aluminium was aimed at. The metal platinum, which is not attacked by the fluorides, cannot be used. for crucibles upon a commercial scale on account of its great cost. TVith a View of avoiding this difficulty our invention com prises the use of the metallic containing-vessel not as the cathode pure and simple, but as a fractional cathodethat is to say, an ordinary or regular cathode is being used, but the containingvessel is made a branch thereof, through which only a small portion of the current passes, whereby the metal of the crucible becomes lined with a line layer of aluminium alloy, by which it is protected against the corrosive action of the melted fluorides, while pure aluminium is deposited upon the caththe bath melts.
to be formed.
from the following detailed description, with,
reference to the accompanying drawings, in which Figure 1 represents a vertical section of an, electrolytic apparatus constructed in accordance with our invention for the production ofaluminium alloys, and Fig. 2 is a like view of. the apparatus as modified for the production the product desired. If it is desired to obtain of pure aluminium.
Like letters of reference indicate like parts of which the containing-vessel is made, then in both figures of the drawings.
In pursuance of the object of our invention We form an electrolytic bath by melting; together either native or artificial cryolite with chloride of sodium or common or marine salt in such proportions that the resulting mass has a specific gravity which is lower than that of aluminium.
As above stated, we may use artificial cryo-f lite, and in so doing we are not obliged toadhere to the proportions of fluoride of alu-. minium and fluoride of sodium as found in Thus, for instance, we may native cryolite.
Fluoride of aluminium 35 Fluoride of sodium 10 Chloride of sodium 55 Total 100 .An electrolytic bath formed bythe melting together of cryolite and chloride of sodium in: such proportions as to give a mass which is; specifically lighter than aluminium also pos-i sesses two other characteristics which are of 3 great value in the production of aluminium? One of these characteristics is its great fluid-i ity, whereby the bath behaves under the ac-{ tion of the current with the same regularityi as a salt in solution, and thatattemperaturesi varying from 900 to 1,100 centigrade, which are the highest temperatures used by us; The second of these characteristics is that the; bath is very little volatile, so that not more thanabout five per cent. of the whole mass is lost in twenty-four hours.
In the practice of our invention for producm g aluminium alloys we use an apparatus constructed in the manner indicated in Fig. 1.
In this figure of the drawings there is shown a containing vessel or crucible I), made of the, metal with which the alloy with aluminium is; It may therefore be made of any of the base metals which readily alloy, with aluminium and which at the same time are refractory at the temperatures at which; This containing vessel or crucible is embedded in fire bricks or clay c: in such a manner that the flame of the fur-Q nace does not directly impinge upon the ves-Q sel, and it is formed with an inclined bottom, as shown, for a purpose which will presently is drained off by opening the orifice T.
appear. At the side of the vessel, close to the lowest point of the bottom of the same, 1s formed an orifice T, which is ordinarily plugged up, but so that it may be opened readily. One or more electrodes A A are sus' pended within the bath and are used as anodes, while the containing-vessel 18 used or may be used as the cathode, so that the current, entering by the electrodes A A, traverses the bath and issues by a conductor connected with the containing-vessel, all as indicated by the arrows in the drawings. The anodes may be made of dilterent materials, according to aluminium moderately alloyed with the metal the anodes will be made of carbon. In this case a small percentage of the metal of 'the containing-vessel alloys with the aluminium liberated; but if it is desired to obtain an alloy coi'itaining a considerable quantity of the metal of which the containing-vessel is made then the anodes are also made of that metal.
The electrolytic bath being made, as above described, specifically lighterthan aluminium, the alloy (1, formed by the use of the apparatus represented in Fig. 1,will flow down along the sides of the containing-Vessel and will accumulate upon the inclined bottom, and after a suitable quantity has thus accumulated hit e time when this is done-that is to say, the time when a sufficient quantity of the deposited metal has accumulated-is easily learned by experience, and may, in fact, be predetermined with great accuracy by computation, since, as above stated, our electrolytic bath behaves with the same regularityas a salt in solution. Knowing, therefore, the volume and electro-motive force of the current employed; knowing, also, the electrical resistance of the bath and the counter electro-motive force of the same, the amount of metal liberated within a certain time can be accurately computed.
For the production of pure aluminium an apparatus like that represented in Fig. .2is used. It consists of .the-containing-vessel l), which in this case has a horizontal bottom and is embedded in fire bricks or clay 0, substantially like the apparatus described with reference to Fig. 1. A plate 6, madcof either fused alumina or of fluoride of calcium, is placed upon the bottom of said vessel, and upon this plate ethere is placed a small crucible d, made of the same material of which the plate e is made, and acathode C, inserted in the bath, reaches down to the bottom of the crucible d, while the anode A rests uponlthe plate e. In this case both the anode and the cathode are made of carbon. NVith the ap paratus so far described if the current were allowed to enter at the anodeA and then pass through the bath to the cathode O and-issue by the same entirely the bath would corrode the containing-vessel and the metal liberated at the cathode would not be pure aluminium but an impure alloy, as hereinbefore stated. This we avoid by making the containing-vessel a fractional cathode-that is to say, the containing-vessel is connected by a high-resistance conductor with the conductor leading from the cathode O to the source of current, as indicated in the drawings. This resistance ris made so great that only about five per cent. of the entire current passes through the containing-vessel, and at no time should there be allowed more than ten per cent. of the current to be diverted through the containing-Vessel. The current thus diverted is not sufficient to produce a considerable quantity of alloyof aluminium with the metal of the vessel, but the effect is to deposit upon the walls of the vessel a thin layer a of such alloy, which effectively protects the vessel against the corrosive action of the bath, while pure aluminium is deposited upon the cathode 0, along the face of which the aluminium flows down and accumulates in the crucible d. Ve are thus enabled to produce aluminium of great purity.
Having now described our invention, we claim and desire to secure by Letters Patent 1. The method of electrolyzing molten aluminium compounds, which consists in passing the main portion of an electric current through the molten mass between electrodes immersed in the same and the remaining fraction of the current between the anode and the containing-vessel, substantially as described.
2. The process of producing aluminium by electrolysis, which consists in first making a molten bath containing fluoride of aluminium and then passing the main portion of an electric current through the bath between electrodes immersed in the bath and the remaining fraction of the current between the anode and the containing-vessel, substantially as described.
The process of producing aluminium by electrolysis, which consists in first making a melted bath which is specifically lighter than aluminium and which contains fluoride of aluminium and chloride of sodium and then passing the main portion of an electric current through the bath between suitable electrodes placed in the bath and the remaining fraction of the current through the anode, the bath, and containing-vessel, substantially as described.
at. The process of producing aluminium by electrolysis,which consists in melting together cryolite and chloride of sodium in such proportions as to form a bath which is specifically lighterthan aluminium and then passing the main portion of an electric current through the bath between an anode and a cathode to the exclusion of the containing-vessel and the remaining fraction of the current through the bath between the anode and the containing-vessel as a fractional cathode, whereby pure aluminium is liberated at the cathode and aluminium alloy is formed upon the containing-vessel, substantially as described.
5. An apparatus for producing aluminium by electrolysis, consisting of a metallic contaming-vessel or crucible for the bath, an anode, a cathode, a depositing-vessel or crucible for the same located within and insulated from the containing-vessel, and a branch conductor of high electrical resistance between the cathode and the containing-vessel, whereby the latter becomes a fractional cathode, substantially as described.
In testimony whereof we have signed our names to this specification in the presence of two subscribing witnesses.
MYRTHIL BERNARD. ERNEST BERNARD.
Witnesses:
RoBT. M. HooPER, ALBERT OAHnNs,
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US476914A true US476914A (en) | 1892-06-14 |
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US476914D Expired - Lifetime US476914A (en) | Myrthil bernard and ernest bernard |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2514283A (en) * | 1944-09-16 | 1950-07-04 | Us Navy | Electrolysis of light metals |
US2762767A (en) * | 1952-02-09 | 1956-09-11 | Int Smelting & Refining Co | Method and means for the prevention of electrolytic corrosion |
US2963413A (en) * | 1959-01-12 | 1960-12-06 | Rolland C Sabins | Electrolytic system |
US3004905A (en) * | 1959-02-09 | 1961-10-17 | Rolland C Sabins | Cathodic protection system |
US3028324A (en) * | 1957-05-01 | 1962-04-03 | British Aluminium Co Ltd | Producing or refining aluminum |
US3201335A (en) * | 1962-02-08 | 1965-08-17 | Shell Oil Co | Corrosion protection |
US3257307A (en) * | 1962-06-11 | 1966-06-21 | Kaiser Aluminium Chem Corp | Electrolytic cell for the production of aluminum |
US3345278A (en) * | 1963-03-25 | 1967-10-03 | Hooker Chemical Corp | Anodic passivation of metals |
US3406103A (en) * | 1965-05-21 | 1968-10-15 | Pittsburgh Plate Glass Co | Method and apparatus for monitoring lining damage of alkali metal chlorate bipolar cells |
US4124465A (en) * | 1972-07-18 | 1978-11-07 | Swiss Aluminium Ltd. | Protecting tube |
US4675084A (en) * | 1985-03-19 | 1987-06-23 | Pechiney | Process for improving the purity of transition metals produced by electrolysis of halides thereof in a bath of molten salts |
-
0
- US US476914D patent/US476914A/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2514283A (en) * | 1944-09-16 | 1950-07-04 | Us Navy | Electrolysis of light metals |
US2762767A (en) * | 1952-02-09 | 1956-09-11 | Int Smelting & Refining Co | Method and means for the prevention of electrolytic corrosion |
US3028324A (en) * | 1957-05-01 | 1962-04-03 | British Aluminium Co Ltd | Producing or refining aluminum |
US2963413A (en) * | 1959-01-12 | 1960-12-06 | Rolland C Sabins | Electrolytic system |
US3004905A (en) * | 1959-02-09 | 1961-10-17 | Rolland C Sabins | Cathodic protection system |
US3201335A (en) * | 1962-02-08 | 1965-08-17 | Shell Oil Co | Corrosion protection |
US3257307A (en) * | 1962-06-11 | 1966-06-21 | Kaiser Aluminium Chem Corp | Electrolytic cell for the production of aluminum |
US3345278A (en) * | 1963-03-25 | 1967-10-03 | Hooker Chemical Corp | Anodic passivation of metals |
US3406103A (en) * | 1965-05-21 | 1968-10-15 | Pittsburgh Plate Glass Co | Method and apparatus for monitoring lining damage of alkali metal chlorate bipolar cells |
US4124465A (en) * | 1972-07-18 | 1978-11-07 | Swiss Aluminium Ltd. | Protecting tube |
US4675084A (en) * | 1985-03-19 | 1987-06-23 | Pechiney | Process for improving the purity of transition metals produced by electrolysis of halides thereof in a bath of molten salts |
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