US2850443A - Method of treating alloys - Google Patents
Method of treating alloys Download PDFInfo
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- US2850443A US2850443A US615489A US61548956A US2850443A US 2850443 A US2850443 A US 2850443A US 615489 A US615489 A US 615489A US 61548956 A US61548956 A US 61548956A US 2850443 A US2850443 A US 2850443A
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- Prior art keywords
- alloy
- sodium
- silicon
- molten
- aluminum
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- 238000000034 method Methods 0.000 title claims description 27
- 229910045601 alloy Inorganic materials 0.000 title description 56
- 239000000956 alloy Substances 0.000 title description 56
- 229910052708 sodium Inorganic materials 0.000 claims description 39
- 239000011734 sodium Substances 0.000 claims description 39
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 37
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 claims description 24
- 229910000676 Si alloy Inorganic materials 0.000 claims description 23
- 239000003792 electrolyte Substances 0.000 claims description 19
- 229910001415 sodium ion Inorganic materials 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 description 17
- 239000002184 metal Substances 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 14
- 238000007792 addition Methods 0.000 description 13
- 239000000654 additive Substances 0.000 description 13
- 230000004048 modification Effects 0.000 description 11
- 238000012986 modification Methods 0.000 description 11
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- 230000000996 additive effect Effects 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- 239000010703 silicon Substances 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 230000005496 eutectics Effects 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 229910001092 metal group alloy Inorganic materials 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 235000011164 potassium chloride Nutrition 0.000 description 5
- 239000001103 potassium chloride Substances 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- -1 sodium modified aluminum-silicon Chemical class 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000007872 degassing Methods 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- KMWBBMXGHHLDKL-UHFFFAOYSA-N [AlH3].[Si] Chemical class [AlH3].[Si] KMWBBMXGHHLDKL-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000006023 eutectic alloy Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910001234 light alloy Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/02—Alloys based on aluminium with silicon as the next major constituent
Definitions
- the present invention relates to the treatment of metal alloys for the purpose of improving their physical properties. More particularly, the invention relates to the production of sodium modified aluminum-silicon alloys.
- sodium is generally added either as metallic sodium or in the form of certain sodium salts, especially the halides such as sodium fluoride, which salts react with the metal alloy and lead to the introduction of sodium.
- the use of sodium salts has the disadvantage of being inefficient and consequently large quantities of salts must be added in order to effect satisfactory modification.
- Use of the salts has a further disadvantage in that the salts tend to corrode the crucibles in which treatment of the molten metal is carried out.
- the application of the salts is a laborious and time consuming operation inevitably causing a delay in casting of the modified alloy.
- metallic sodium While more etficient with respect to the addition of sodium to the alloy, has the serious disadvantage of introducing an appreciable quantity of dissolved hydrogen into the molten aluminum-silicon alloy.
- the hydrogen gas results from the parafiin or oil which is generally used as a protective medium for the metallic sodium.
- the metallic sodium is also contaminated with moisture containing products which are violently driven ofi at the temperature of addition to the alloy causing splattering of both the molten alloy and sodium. All of these contaminants are sources of impurities and the metallic sodium used for modification purposes is often the cause of gas porosity problems in the cast aluminum-silicon alloy.
- the principal object of the present invention to provide a novel method for treating alloys with additions of low melting point additives which prevents the introduction of undesirable contaminants and which is efficient and economical to perform and can be easily and safely carried out to produce a metal alloy having improved physical properties.
- a more detailed object of the present invention is to provide a method of the foregoing type for modifying an aluminum-silicon alloy with sodium without introducing hydrogen and other contaminants.
- a related object is to add sodium modifiers to aluminum-silicon alloys more efiiciently and economically for producing an alloy having a refined microstructure and improved physical properties.
- the desired treatment of a metal or metal alloy with a reactive metal additive is accomplished by the novel method which comprises contacting a molten bath of the alloy to be treated with a layer of fused salts, such as oxides or halides, of the metal additive, in a flux carrier and electrolyzing the salt layer or electrolyte with the molten alloy as one electrode.
- a second electrode generally formed of carbon, is inserted in the molten supernatant layer of fused electrolyte and upon application of an electric current, the electrolyte salts are electrolyzed to discharge the desired metal as an ion into the molten alloy which is being treated.
- the molten alloy will be made the cathode. It is understood however, that the polarity may be reversed and the molten alloy may be made the anode when the element to be introduced is contained in the anions of the electrolytic layer.
- the fused salt in its flux carrier is electrolyzed so that the element to be introduced is discharged as a cation at the molten alloy surface and introduced into the molten alloy.
- quantity of metal additive introduced into the molten alloy, the electrolyzing current, or alternatively the time forwhich a given current is applied, is varied. It is thus possible to control very accurately the amount of metal additive to be introduced for accomplishing a desired treatment.
- furnace charges of this alloy normally consist of a mixture of foundry returns and new ingot metal.
- the ratio of modified returns to new ingot is seldom constant over a number of consecutive melts and, therefore, the amount ofsodium in any one furnace charge is difficult to estimate.
- the practice which is followed by the majority of light alloy founders is to destroy all existing traces of modification and then to remodify with a controlled amount of modifying agent. In this way the exact state of modification of the melt is known and can be varied at will to suit different casting sections.
- degassing serves the dual purpose of removing small quantities of dissolved hydrogen which may have been absorbed during the melting of the alloy and destroying all traces of existing sodium modification.
- a molten bath of the alloy is placed in a suitable container and in contact with an electrode.
- An electrolytic layer consisting of sodium chloride and potassium chloride carried in a fluxis then floated on the molten alloy.
- the supernatant electrolytic layer is desirably a fused liquid and can be either prefused or fused after the salts have been placed on the molten alloy.
- An anode in theform of a carbon electrode is inserted into the fused electrolytic layer.
- an electrolyzing current is applied between the anode and the molten alloy as the cathode.
- the sodium cations are discharged at the alloy surface and are thereby introduced into the molten alloy.
- the anions produced by the electrolysis migrate towards the anode where they are discharged and collected, if desired, although the amount of such anions is ordinarily very small.
- a novel and improved method for the production of trolyte containing sodium ions is electrolyzed with .a
- the method of modifying an aluminum-silicon alloy with sodium which comprises the steps of forming a molten bath of aluminum-silicon alloy, adding an alkaline chloride electrolyte as a source of sodium ions, inserting an electrode into saidelectrolyte, and electrolyzing said electrolyte with said electrode as an anode and said molten alloy as a cathode to remove sodium ions from said electrolyte and introduce sodium ions into said alloy for modifying the same.
- the method of modifying an aluminum-silicon alloy by additions of sodium which comprises electrolyzing a molten alkaline chloride electrolyte containing sodium ions with an anode inserted in said electrolyte and with 2,850,443 a cathode consisting of the aluminum-silicon alloy in a trolyte with said carbon electrode as an anode and said molten state. molten alloy as a cathode to remove sodium ions from 6.
- the method of claim 5 wherein the electrolysis is said electrolyte and introduce said sodium ions into the stopped When the cathode metal has acquired enough alloy for modifying the same. sodium to be Well modified.
- 5 9.
- the electrolyte 7 The method of claim 5 wherein the molten eleccomprises sodium chloride and potassium chloride. trolyte comprises sodium chloride and potassium chloride.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Metals (AREA)
Description
United States Patent METHOD OF TREATING ALLOYS David Valentine Atterton, Solihull, England, assignor to Foundry Services Limited, Birmingham, England, a British company No Drawing. Application October 12, 1956 Serial No. 615,489
Claims priority, application Great Britain October 12, 1955 9 Claims. (Cl. 204-71) The present invention relates to the treatment of metal alloys for the purpose of improving their physical properties. More particularly, the invention relates to the production of sodium modified aluminum-silicon alloys.
In common foundry practice additions of low melting point, highly reactive metals to metal alloys are made for the general purpose of improving the physical properties of the alloys. While these additions are desirable in that they serve to modify or refine the grain structure' of the alloys, the addition of the modifying elements is difficult to accomplish in most cases because the low melting point metals being added are slow to dissolve and difficulties are experienced in bringing the additives into intimate contact with the molten alloy. Because the molten alloy is often at a much higher temperature than the melting point of the additive, there is a danger that the latter will boil and become oxidized at the surface of the molten alloy before an effective amount is added to the body of the alloy. The boiling and oxidation of the additives on the surfaces of the molten alloy causes splattering, fuming and burning which is dangerous and is desirably avoided. It has been found, too, that when salts, such as halides or oxides, of the above additive metals are used to avoid the hazardous reactions occurring when the pure metal additive is used, the efliciency of addition is extremely low and a large excess of salts must be used to accomplish the desired treatment.
In the production of aluminum-silicon alloys the properties of the alloy are considerably altered and improved by the introduction of small quantities of metallic sodium. Sodium, of course, is highly reactive at the temperature of its introduction to this particular alloy. Silicon, at room temperature, is almost insoluble in aluminum and, therefore, as the unmodified aluminum-silicon alloy solidifies, silicon is precipitated either as a primary constituent or in a eutectic alloy with aluminum. The excess silicon remaining over that forming the eutectic takes the form of coarse plates and needles, and this coarse structure, which is inherently brittle, gives the unmodified alloy poor mechanical properties.
The addition of sodium, either in the form of salts or metallic sodium, has been found to increase the possible silicon content of the aluminum-silicon eutectic to about 13% and, therefore, alloys containing less than this amount of silicon will not exhibit primary silicon crystals. In addition, the aluminum-silicon eutectic is considerably refined and the silicon in excess of that amount required to form the eutectic is precipitated in a fine globular form and not as coarse needles. It is this refinement of the microstructure which enhances the mechanical properties of the alloy. As a result of the treatment of the molten aluminum-silicon alloy with sodium, the physical properties of the alloy are considerably altered and improved. Such treatment is known to those skilled in foundry practices as modification and leads to a. considerable refinement of the microstructure 2,856,443 Patented Sept. 2, 1958 of the aluminum-silicon alloy with an improvement in both tensile strength and elongation of the alloy.
In accordance with the usual foundry practice, sodium is generally added either as metallic sodium or in the form of certain sodium salts, especially the halides such as sodium fluoride, which salts react with the metal alloy and lead to the introduction of sodium. The use of sodium salts has the disadvantage of being inefficient and consequently large quantities of salts must be added in order to effect satisfactory modification. Use of the salts has a further disadvantage in that the salts tend to corrode the crucibles in which treatment of the molten metal is carried out. Furthermore, the application of the salts is a laborious and time consuming operation inevitably causing a delay in casting of the modified alloy.
The use of metallic sodium, on the other hand, While more etficient with respect to the addition of sodium to the alloy, has the serious disadvantage of introducing an appreciable quantity of dissolved hydrogen into the molten aluminum-silicon alloy. The hydrogen gas results from the parafiin or oil which is generally used as a protective medium for the metallic sodium. The metallic sodium is also contaminated with moisture containing products which are violently driven ofi at the temperature of addition to the alloy causing splattering of both the molten alloy and sodium. All of these contaminants are sources of impurities and the metallic sodium used for modification purposes is often the cause of gas porosity problems in the cast aluminum-silicon alloy. Additions of sodium in the metallic form, in addition to having the above-mentioned disadvantages of carrying contaminants which are the source of hydrogen, is more expensive because it involves the additional steps of producing and refining metallic sodium of 511thcient purity to avoid as much as possible the danger of contaminating the aluminum-silicon alloy with undesirable impurities.
It is, therefore, the principal object of the present invention to provide a novel method for treating alloys with additions of low melting point additives which prevents the introduction of undesirable contaminants and which is efficient and economical to perform and can be easily and safely carried out to produce a metal alloy having improved physical properties.
A more detailed object of the present invention is to provide a method of the foregoing type for modifying an aluminum-silicon alloy with sodium without introducing hydrogen and other contaminants. A related object is to add sodium modifiers to aluminum-silicon alloys more efiiciently and economically for producing an alloy having a refined microstructure and improved physical properties.
While the invention described herein is susceptible of various modifications, a certain illustrative method will be described in detail. It should be understood, however, that there is no intention to limit the invention to the specific form disclosed but, on the contrary, the intention is to cover all modifications, alternatives and equivalents falling within the spirit and scope of the invention as expressed in the appended claims.
In accordance with the present invention the desired treatment of a metal or metal alloy with a reactive metal additive is accomplished by the novel method which comprises contacting a molten bath of the alloy to be treated with a layer of fused salts, such as oxides or halides, of the metal additive, in a flux carrier and electrolyzing the salt layer or electrolyte with the molten alloy as one electrode. A second electrode, generally formed of carbon, is inserted in the molten supernatant layer of fused electrolyte and upon application of an electric current, the electrolyte salts are electrolyzed to discharge the desired metal as an ion into the molten alloy which is being treated. If the metal additive to be introduced is a cation, the molten alloy will be made the cathode. It is understood however, that the polarity may be reversed and the molten alloy may be made the anode when the element to be introduced is contained in the anions of the electrolytic layer.
Upon application of an electric current and: to the electrolyzing circuit, the fused salt in its flux carrier is electrolyzed so that the element to be introduced is discharged as a cation at the molten alloy surface and introduced into the molten alloy. quantity of metal additive introduced into the molten alloy, the electrolyzing current, or alternatively the time forwhich a given current is applied, is varied. It is thus possible to control very accurately the amount of metal additive to be introduced for accomplishing a desired treatment. i
In the production of aluminum-silicon alloys furnace charges of this alloy normally consist of a mixture of foundry returns and new ingot metal. The ratio of modified returns to new ingot is seldom constant over a number of consecutive melts and, therefore, the amount ofsodium in any one furnace charge is difficult to estimate. The practice which is followed by the majority of light alloy founders is to destroy all existing traces of modification and then to remodify with a controlled amount of modifying agent. In this way the exact state of modification of the melt is known and can be varied at will to suit different casting sections.
Sodium modification is destroyed through degassing by the scavenging action of the degasser on the sodium contained in the melt. With aluminum-silicon alloys, therefore, degassing serves the dual purpose of removing small quantities of dissolved hydrogen which may have been absorbed during the melting of the alloy and destroying all traces of existing sodium modification.
For the purpose of adding sodium metal to the degassed aluminum-silicon alloy by the method embodying the present invention, a molten bath of the alloy is placed in a suitable container and in contact with an electrode. An electrolytic layer consisting of sodium chloride and potassium chloride carried in a fluxis then floated on the molten alloy. The supernatant electrolytic layer is desirably a fused liquid and can be either prefused or fused after the salts have been placed on the molten alloy. An anode in theform of a carbon electrode is inserted into the fused electrolytic layer.
In order to introduce sodium into the molten alloy, an electrolyzing current is applied between the anode and the molten alloy as the cathode. The sodium cations are discharged at the alloy surface and are thereby introduced into the molten alloy. The anions produced by the electrolysis migrate towards the anode where they are discharged and collected, if desired, although the amount of such anions is ordinarily very small. When the desired amount of sodium has been deposited, as determined by the amount of current and the length of time the electrolyte is subject to electrolysis, the current is shut off and the container of modified alloy and the alloy castinto suitable molds.
To illustrate the above-described novel method, the following example is presented.
is tapped Example A melt of aluminum-silicon alloy, after degassing, was analyzed and contained 0.0005% by Weight of sodium. This alloy was placed in a crucible and an electrolyte containing sodium chloride, potassium chloride, and a flux was floated on its surface. A carbon electrode was then inserted into the molten metal, being insulated from the electrolyte. A carbon anode was inserted into the supernatant electrolyte and a potential of volts was applied between the anode and the molten metal cathode. With this arrangement a current of approxi In order to control the Average mechanical properties Unmodified Modified alloy alloy Ultimate tensile strength (ton/sq. in.) 7.0 11. 5 Elongation (percent on 2 in.) 3. 0 8.0
By using the above described electrolytic method for modifying an aluminum-silicon alloy with sodium, .it can be seen that the efiiciency of the addition of sodium has been substantially increased over the older methods of adding sodium, such as by reacting sodium salts with the alloy or by adding sodium metal, in which it was possible to add an amount of sodium only to the extent of about 0.020% of the weight of the alloy. The efficiency of conversion of the available sodium is thus quite high with the present invention as compared with older methods, making the herein described novel method particularly desirable for use with alloys having a high silicon content. It is to be further noted that by carrying out the sodium modification electrolytically, it is unnecessary to purify or otherwise treat the sodium metal or salt to be added. The electrolytic method is selective for sodium ions and the introduction of impurities into the alloy is thereby prevented.
A novel and improved method for the production of trolyte containing sodium ions is electrolyzed with .a
cathode of molten aluminum-silicon alloy into which the sodium is to be introduced for purposes of modifica tion. An efiicient and economical method for such treatment is thus attained, which method eliminates the necessity of procuring and purifying a sodium metal additive and further eliminates any undesirable reactions of the additive with the molten alloy at the temperature at which the addition must be made. In addition, the novel method, by ionizing the sodium, affords a more intimate contact of the modifying element with the alloy. It thus becomes possible to modify alloys having a high silicon content to form a silicon-aluminum eutectic and cause the excess silicon to precipitate in fine globules instead of brittle needles and plates.
I claim as my invention:
1. The method of modifying an aluminum-silicon alloy with sodium which comprises the steps of forming a molten bath of aluminum-silicon alloy, adding an alkaline chloride electrolyte as a source of sodium ions, inserting an electrode into saidelectrolyte, and electrolyzing said electrolyte with said electrode as an anode and said molten alloy as a cathode to remove sodium ions from said electrolyte and introduce sodium ions into said alloy for modifying the same. A 1
2. The method of claim 1 wherein an electrolyzing current of about 45 amperes is applied for a period of about ten minutes.
3. The method of claim 1 wherein the molten electrolyte comprises sodium chloride and potassium chloride.
4. The method of claim 1 wherein the electrolysis is stopped when the cathode metal acquires a sodium content of about 0.0293%.
5. The method of modifying an aluminum-silicon alloy by additions of sodium which comprises electrolyzing a molten alkaline chloride electrolyte containing sodium ions with an anode inserted in said electrolyte and with 2,850,443 a cathode consisting of the aluminum-silicon alloy in a trolyte with said carbon electrode as an anode and said molten state. molten alloy as a cathode to remove sodium ions from 6. The method of claim 5 wherein the electrolysis is said electrolyte and introduce said sodium ions into the stopped When the cathode metal has acquired enough alloy for modifying the same. sodium to be Well modified. 5 9. The method of claim 8 wherein the electrolyte 7. The method of claim 5 wherein the molten eleccomprises sodium chloride and potassium chloride. trolyte comprises sodium chloride and potassium chloride.
8. The method of modifying the microstructure of References Cited in the file of this Pawnt an aluminum-silicon alloy with additions of sodium metal UNITED STATES PATENTS which comprises the steps of forming a molten bath of 10 the alloy, adding a supernatant alkaline chloride elecg g? f 5; trolyte as a source of sodium ions, inserting a carbon um ay electrode into said electrolyte and electrolyzing said elec- 2013926 Pacz Sept 1935
Claims (1)
1. THE METHOD OF MODIFYING AN ALUMINUM-SILICON ALLOY WITH SODIUM WHICH COMPRISES THE STEPS OF FORMING A MOLTEN BATH OF ALUMINUM-SILICON ALLOY, ADDING AN ALKALINE CHLORIDE ELECTROLYTE AS A SOURCE OF SODIUM IONS, INSERTING AN ELECTRODE INTO SAID ELECTROLYTE, AND ELECTROLYZING SAID ELECTROLYTE WITH SAID ELECTRODE AS AN ANODE AND SAID MOLTEN ALLOY AND INTRODUCE SODIUM IONS INTO SAID ALLOY FOR MODIFYING THE SAME.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2850443X | 1955-10-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2850443A true US2850443A (en) | 1958-09-02 |
Family
ID=10916491
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US615489A Expired - Lifetime US2850443A (en) | 1955-10-12 | 1956-10-12 | Method of treating alloys |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2850443A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3265606A (en) * | 1961-03-29 | 1966-08-09 | Montedison Spa | Electrolytic cell for preparation of alloys of lead with alkaline metals |
| US5873993A (en) * | 1994-06-07 | 1999-02-23 | Stubergh; Jan | Method and apparatus for the production of silicium metal, silumin and aluminium metal |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1464625A (en) * | 1920-03-18 | 1923-08-14 | Pacz Aladar | Electrolyte for aluminum production and method of preparing same |
| US1910017A (en) * | 1927-12-21 | 1933-05-23 | Alais & Froges & Camarque Cie | Electrolytio extraction of light metals contained in alloys |
| US2013926A (en) * | 1930-08-23 | 1935-09-10 | Pacz Aladar | Modification of aluminum, aluminum alloys, and alloys containing aluminum |
-
1956
- 1956-10-12 US US615489A patent/US2850443A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1464625A (en) * | 1920-03-18 | 1923-08-14 | Pacz Aladar | Electrolyte for aluminum production and method of preparing same |
| US1910017A (en) * | 1927-12-21 | 1933-05-23 | Alais & Froges & Camarque Cie | Electrolytio extraction of light metals contained in alloys |
| US2013926A (en) * | 1930-08-23 | 1935-09-10 | Pacz Aladar | Modification of aluminum, aluminum alloys, and alloys containing aluminum |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3265606A (en) * | 1961-03-29 | 1966-08-09 | Montedison Spa | Electrolytic cell for preparation of alloys of lead with alkaline metals |
| US5873993A (en) * | 1994-06-07 | 1999-02-23 | Stubergh; Jan | Method and apparatus for the production of silicium metal, silumin and aluminium metal |
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