US3208922A - Galvanic process for coating iron alloys with magnesium hydroxide - Google Patents
Galvanic process for coating iron alloys with magnesium hydroxide Download PDFInfo
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- US3208922A US3208922A US108723A US10872361A US3208922A US 3208922 A US3208922 A US 3208922A US 108723 A US108723 A US 108723A US 10872361 A US10872361 A US 10872361A US 3208922 A US3208922 A US 3208922A
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- magnesium hydroxide
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D9/00—Electrolytic coating other than with metals
- C25D9/04—Electrolytic coating other than with metals with inorganic materials
- C25D9/08—Electrolytic coating other than with metals with inorganic materials by cathodic processes
- C25D9/10—Electrolytic coating other than with metals with inorganic materials by cathodic processes on iron or steel
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/54—Contact plating, i.e. electroless electrochemical plating
Definitions
- the grain oriented silicon steels referred to may be made by several well known commercial processes which usually include the following steps: A ferrous alloy containing up to about 6% silicon and relatively minor amounts of impurities is cast into ingots; hot worked, usually by rolling as a continuous strand; and then subjected to varying schedules of usually unidirectional cold rolling. The steel is then heat treated byseveral combinationsof treating cycles which cause primary recrystallization of the grains,
- the grain orientation of the magnetic steels produced by the above type of process is usually referred to as the (110) [001] type in the standard notation by Millers Indices. This designation is intended to indicate that the [001] direction of the crystals is parallel to the rolling direction and the (110) plane is parallel to the rolling plane. Considering the crystals as cubes, the designation indicates a cube on edge position of the crystal in the plane of a sheet of the material. It is to be understood, of course, that the specific process by which such steels are made forms no part of the present invention.
- magnesium silcate is normal ly obtained by applying magnesium hydroxide to semi-processed silicon steels and then heating at high temperatures during the final grain growth and purification anneal of the steel.
- Mg SiO coating is normal ly obtained by applying magnesium hydroxide to semi-processed silicon steels and then heating at high temperatures during the final grain growth and purification anneal of the steel.
- a chemical reaction takes place in which the water of hydration of the magnesium hydroxide is driven off and the resulting magnesium oxide (MgO) is available to combine with silicon in the steel to form an adherent, refractory, high strength'electrical insulating and high temperature separating coating of magnesium silicate.
- This invention is directed to an improved process for depositing magnesium hydroxide on iron alloys, such as the magnetic steels described above.
- Examples of prior art processes for applying magnesium hydroxide to magnetic steels are (l) passing the steel through a water slurry of magnesium oxide, and (2) depositing the magnesium hydroxide on the steel in electrolytic processes in which external current is required.
- the water slurry processes possess disadvantages in that the deposited coating often lacks uniformity in thickness with resulting Accordingly, it is an object of this invention to provide.
- Another object of the invention is to provide a process for galvanically coating iron alloys with magnesium hydroxide.
- Another object of the invention is to provide an improved process for coating silicon steels with a uniform magnesium hydroxide coating without the application of an external current, the magnesium hydroxide coatings being suitable for conversion into magnesium silicate coatings.
- a further object of the invention is to provide an improved process for obtaining electrical insulating and high temperature separating coatings on grain oriented silicon steels.
- Another object of the invention is to provide a galvanic process for coating iron alloys with magnesium hydroxide in which the electrolytic salt isnot consumed.
- Another object of the invention is to provide an improved process for coating thin sheets of grain oriented silicon steel in which the edges of the sheet are coated, the process being characterized by the absence of an external current.
- a coating of magnesium hydroxide may be deposited on iron alloys by a galvanic process in which an iron alloy article is immersed in a water solution of a magnesium salt; a magnesium metal article is also immersed in the solution; and the iron alloy article and magnesium metal article are electrically connected to each other.
- the electrolyte should be a water solution of a magnesium salt, and magnesium acetate [Mg(C H O magnesium chloride-(MgGl magnesium nitrate [Mg( 0s)z]. and magnesium sulfate [Mg(SO have all been successfully employed as the salt.
- concentration of the salt should be between about 10 grams per liter and 100 grams per liter.
- Table I results obtained for magnesium hydroxide coatings deposited on grain oriented silicon steeL.
- the steel' was a commercially available, 3%% silicon alloy, havinga (110) [001] type of grain orientation, and a thickness of .012".
- the steel was semi-processed in that'it had not-been given its final grain growth and purification anneal.
- the anode was'magnesium metal, and consisted of an assembly of two banks of ,4 diameter commercially pure magnesium rods which were 6 inches in length, and embedded at one end in a rectangular copper holder. Each bank was formed by placing six rods next to each other in the longer sides of the copper holder with the rods being spaced about A" apart.
- the silicon steel strip being coated was placed 'midway between the two banks of magnesium rods' and connected to the rods by means of a copper wire grounded to the copper holder.
- the silicon steel strips measured 6" x 1" and were approximately one inch away from either. bank of magnesium rods.
- the assembly was then lowered into a water solution of a magnesium salt with the magnesium and steel members, but not the copper holder or wire, being immersed.
- the formation of bubbles was immcdiately noted atthe surface ,of the steel, and it was also apparent'that a cotaing was being produced. on the steel.
- the iron and .magnesium were immersed in the electrolyte for about 3 minutes.
- the values Y n for coating weight are based on the weight of the magnesium hydroxide coating deposited on the surface area of the steel strips.
- the Franklin insulation values were for magnesium silicate coatings produced by taking the silicon steel speci-' mens coated. with magnesium hydroxide andgiving them tion anneal in dry hydrogen for 8 hours at 1175 C. In the standard Franklin test employed, readings of l ampere represent no-surface insulation and readings of Generally speaking, Franklin insulation values belowabout 0.4 ampere are preferred for highvoltage electrical applications. Higher Franklin values (i.e., less insulation strength) are acceptable in some applications where high voltages are not encountered.
- magnesium ions are replenished. by-thedissolution of the Mg anode. salt'is not used up but merely acts as a conductor.
- the materials consumed in this process are the magnesium and water.
- the coatings were uniform in thickness and were tenaciously bonded to all surfaces of .the steel strips including the thin edges.:
- the coating weights were in the range of from about .010 to .030 ounce per square foot. Table I shows that coatingshaving excellent electrical insulation properties were obtained after various combinations of electrolyte concentration and temperature had been employed. Coatings with Franklin values below 0.4 ampere were also obtained with the magnesium chloride given their final grain growth and purification anneal, during which anneal an electrical insulating and high temperature separating magnesium silicate coating is produced on the exterior surface of the steel.
- the process comprising arranging an iron alloy member and a magnesium metal member directly electrically connected to each other in a water solution having a concentration of above. about grams per liter of a magnesium salt for sufiicient time to deposit a magnesium hydroxide coating on the iron alloy member by galvanic action, and recovering the thus coated iron alloy member.
- a galvanic coating process for depositing magnesium hydroxide on an iron alloy article comprising: immersing the iron alloy article in a water solution having a concentration of above about 10 grams per liter of a magnesium salt at a temperature about about 25 C., immersing a magnesium article in said solution, and directly connecting said iron alloy article to said magnesium article through an electrical conductor.
- a galvanic coating process for depositing magnesium hydroxide on an iron alloy article comprising: immersing the iron alloy article in a water solution having a magnesium salt concentration above about 10 grams per liter, immersing a magnesium article in said solution, and directly connecting said iron alloy article to said magnesium article through an electrical conductor.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
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- Chemical Treatment Of Metals (AREA)
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Description
United States Patent Ofice 3,208,922 GALVANIC PROCESS FOR COATING IRON ALLOYS WITH MAGNESIUM HYDROXIDE James M. McQuade, Pittsfield, Mass., assignor to General Electric Company, a corporation of New York No Drawing. Filed May 9, 1961, Ser. No. 108,723
' 8 Claims. (Cl. 204-56) annealed at high temperatures. The grain oriented silicon steels referred to may be made by several well known commercial processes which usually include the following steps: A ferrous alloy containing up to about 6% silicon and relatively minor amounts of impurities is cast into ingots; hot worked, usually by rolling as a continuous strand; and then subjected to varying schedules of usually unidirectional cold rolling. The steel is then heat treated byseveral combinationsof treating cycles which cause primary recrystallization of the grains,
decarburization, secondary recrystallization of the grains,
and purification by removal of sulfur and other impurities. The grain orientation of the magnetic steels produced by the above type of process is usually referred to as the (110) [001] type in the standard notation by Millers Indices. This designation is intended to indicate that the [001] direction of the crystals is parallel to the rolling direction and the (110) plane is parallel to the rolling plane. Considering the crystals as cubes, the designation indicates a cube on edge position of the crystal in the plane of a sheet of the material. It is to be understood, of course, that the specific process by which such steels are made forms no part of the present invention.
One material that is suitable for use as an electrical insulating and high temperature separating coating on magnetic silicon steels of the typedescribed above is magnesium silcate (Mg SiO coating is normal ly obtained by applying magnesium hydroxide to semi-processed silicon steels and then heating at high temperatures during the final grain growth and purification anneal of the steel. During the high temperature anneal a chemical reaction takes place in which the water of hydration of the magnesium hydroxide is driven off and the resulting magnesium oxide (MgO) is available to combine with silicon in the steel to form an adherent, refractory, high strength'electrical insulating and high temperature separating coating of magnesium silicate. It is to be understood that the specific process by which a magnesium hydroxide coating on such steels is converted into magnesium silicate forms no part of the present invention.
This invention is directed to an improved process for depositing magnesium hydroxide on iron alloys, such as the magnetic steels described above. Examples of prior art processes for applying magnesium hydroxide to magnetic steels are (l) passing the steel through a water slurry of magnesium oxide, and (2) depositing the magnesium hydroxide on the steel in electrolytic processes in which external current is required. The water slurry processes possess disadvantages in that the deposited coating often lacks uniformity in thickness with resulting Accordingly, it is an object of this invention to provide.
' an improved process for coating iron alloys.
Another object of the invention is to provide a process for galvanically coating iron alloys with magnesium hydroxide.
Another object of the invention is to provide an improved process for coating silicon steels with a uniform magnesium hydroxide coating without the application of an external current, the magnesium hydroxide coatings being suitable for conversion into magnesium silicate coatings.
A further object of the invention is to provide an improved process for obtaining electrical insulating and high temperature separating coatings on grain oriented silicon steels.
Another object of the invention is to provide a galvanic process for coating iron alloys with magnesium hydroxide in which the electrolytic salt isnot consumed.
Another object of the invention is to provide an improved process for coating thin sheets of grain oriented silicon steel in which the edges of the sheet are coated, the process being characterized by the absence of an external current.
Other objects and advantages of the invention will become apparent from the following detailed description, and the scope of the invention will be pointed out in the claims.
Briefly stated, according to one aspect of the invention, a coating of magnesium hydroxide may be deposited on iron alloys by a galvanic process in which an iron alloy article is immersed in a water solution of a magnesium salt; a magnesium metal article is also immersed in the solution; and the iron alloy article and magnesium metal article are electrically connected to each other.
My experiments have shown that an adherent magnesium hydroxide coating can be deposited on iron alloys with about and above iron content by a galvanic process. The iron alloy is used as the cathode and magnesium metal is used as the anode. Anodesof commercially pure metallic calcium, zinc, and aluminum were tried without success. The electrolyteshould be a water solution of a magnesium salt, and magnesium acetate [Mg(C H O magnesium chloride-(MgGl magnesium nitrate [Mg( 0s)z]. and magnesium sulfate [Mg(SO have all been successfully employed as the salt. The concentration of the salt should be between about 10 grams per liter and 100 grams per liter. No gain in results was obtained from concentrations above about 100 grams per liter, and when the concentration is decreased below 25 grams per liter, the. immersion coating time should be increased. Thetemperature of the electrolyte should be above about 25 C in that the weight of the deposited coating is a function of temperature; for temperatures below 25 C. the coating immersion time had to be increased beyond commercially practical limits. No gain in results was found when the electrolyte temperature was raised above about C. The above-described processes can be successfully employed for depositing magnesium hydroxide on 50% iron-50% nickel alloys. However, satisfactory results Patented Sept. 28, 1965 ampere represent perfect insulation.
i could not be obtained when copper or aluminum are used as the cathode.
By way of illustration, listed below in Table I are results obtained for magnesium hydroxide coatings deposited on grain oriented silicon steeL. The steel'was a commercially available, 3%% silicon alloy, havinga (110) [001] type of grain orientation, and a thickness of .012". The steel was semi-processed in that'it had not-been given its final grain growth and purification anneal. The anode was'magnesium metal, and consisted of an assembly of two banks of ,4 diameter commercially pure magnesium rods which were 6 inches in length, and embedded at one end in a rectangular copper holder. Each bank was formed by placing six rods next to each other in the longer sides of the copper holder with the rods being spaced about A" apart. The silicon steel strip being coated was placed 'midway between the two banks of magnesium rods' and connected to the rods by means of a copper wire grounded to the copper holder. The silicon steel strips measured 6" x 1" and were approximately one inch away from either. bank of magnesium rods. The assembly was then lowered into a water solution of a magnesium salt with the magnesium and steel members, but not the copper holder or wire, being immersed. The formation of bubbleswas immcdiately noted atthe surface ,of the steel, and it was also apparent'that a cotaing was being produced. on the steel. In all of the exampleslisted in Table I, the iron and .magnesium were immersed in the electrolyte for about 3 minutes. The values Y n for coating weight are based on the weight of the magnesium hydroxide coating deposited on the surface area of the steel strips. The Franklin insulation values were for magnesium silicate coatings produced by taking the silicon steel speci-' mens coated. with magnesium hydroxide andgiving them tion anneal in dry hydrogen for 8 hours at 1175 C. In the standard Franklin test employed, readings of l ampere represent no-surface insulation and readings of Generally speaking, Franklin insulation values belowabout 0.4 ampere are preferred for highvoltage electrical applications. Higher Franklin values (i.e., less insulation strength) are acceptable in some applications where high voltages are not encountered.
TableI- 1 Average for two specimens. I
The final coatings on all samples were refractory and electrolyte in only ninety seconds under the same concentration and temperature conditions as samples 10 and 11. Franklin values of between 0.5 and. 0.7 ampere a standard high temperature grain growth and purificawere obtained with the magnesium acetate electrolyte in only ninety seconds under the same concentration and temperature conditions as samples 4 and 5. Thus, when' the Franklin insulation strength need not be below 0.4 ampere, the immersion-coating time can be reduced accordingly.
The over-all reaction for a galvanic coating process in accord with my teachings is as follows:
Ms+ H= M H .+H= The over-all reaction is brought about'by the following re-actions: Water dissociates to produce hydrogen ions and hydroxyl ions:
' madca- 1 Magnesium goes into solution to produce magnesium The hydrogen ions are discharged to form hydrogen gas 'at the surface of the' iron leaving an excess of 0H.
(Equation 1.) 1 2H++2e-H5 Magnesium ions'from the electrolyte migrate to the iron alloy (cathode) where they combine withthe excess hydroxyl ions and deposit magnesium hydroxide on the surface of the iron alloy:
These magnesium ions are replenished. by-thedissolution of the Mg anode. salt'is not used up but merely acts as a conductor. Thus the materials consumed in this process are the magnesium and water. This makes it easy to controlthe .process over extended periodsof time in that'theamount of magnesium present is readily ascertained merely by observation, and the magnesium can be replenished by inserting other magnesium articles in the electrolyte and connecting them to the iron alloy. It is easy to determine the amount of water being used merely by'observing the level of the electrolyte solution. Also, since water is being consumed, the concentration of the solution becomes stronger; this means that the process will not produce poor results if the water levelis inadvertently allowed to fall.
It has thus been shown that by the practiceof my invention, uniform, adherent magnesium hydroxide coatings can be deposited on iron alloys-by a galvanic process that'does not require the application of an external current.- The process has the advantage .of permitting accurate control of the thickness and weight of'the coating by proper combination of salt concentration, temperature, and immersion coating time, with a resulting uniformity of properties being assured. My process is thus adaptable-for use as a step in large scale continuous strand production operations in which grain oriented electrical silicon steels are continuously processed by coating them with. magnesium hydroxide before they are showed good high temperature'separatio'n properties.
The coatings were uniform in thickness and were tenaciously bonded to all surfaces of .the steel strips including the thin edges.: The coating weights were in the range of from about .010 to .030 ounce per square foot. Table I shows that coatingshaving excellent electrical insulation properties were obtained after various combinations of electrolyte concentration and temperature had been employed. Coatings with Franklin values below 0.4 ampere were also obtained with the magnesium chloride given their final grain growth and purification anneal, during which anneal an electrical insulating and high temperature separating magnesium silicate coating is produced on the exterior surface of the steel.
It will be understood, of course, that while the forms of the invention herein described constitute preferred embodiments of the invention, it is not intended herein to describe all of the equivalent forms or ramifications thereof. Itwillalso be understood that: the words used are words of description rather than of limitation; and that various changes may be made without departing from the spirit or scope of the invention herein disclosed, and it is aimed in the appended claims to cover'all such (Equation 2.) The magnesium changes as fall within the true spirit and scope of the invention.
What I claim as new and desire to secure by Letters Patent of the United States is:
1. The process comprising arranging an iron alloy member and a magnesium metal member directly electrically connected to each other in a water solution having a concentration of above. about grams per liter of a magnesium salt for sufiicient time to deposit a magnesium hydroxide coating on the iron alloy member by galvanic action, and recovering the thus coated iron alloy member.
2. A galvanic coating process for depositing magnesium hydroxide on an iron alloy article comprising: immersing the iron alloy article in a water solution having a concentration of above about 10 grams per liter of a magnesium salt at a temperature about about 25 C., immersing a magnesium article in said solution, and directly connecting said iron alloy article to said magnesium article through an electrical conductor.
3. A galvanic coating process for depositing magnesium hydroxide on an iron alloy article comprising: immersing the iron alloy article in a water solution having a magnesium salt concentration above about 10 grams per liter, immersing a magnesium article in said solution, and directly connecting said iron alloy article to said magnesium article through an electrical conductor.
4. In the process for coating a magnetic steel article having up to about 6% silicon content with a uniform, adherent, refractory magnesium silicate coating having electrical insulating and high temperature separating properties, said process requiring depositing a film of magnesium hydroxide on the surface of the steel article and then annealing at an elevated temperature, the improvement in a method for depositing the magnesium hydroxide on the steel article comprising: immersing the steel article in water-solution having a magnesium salt concentration above about 10 grams per liter at a temperature above about 25 C., immersing a magnesium article in said solution, and directly connecting said steel article and said magnesium article through an electrical conductor, whereby magnesium hydroxide will be deposited on the steel by galvanic action.
5. In the process for coating 2. grain oriented magnetic steel article having up to about 6% silicon content with a uniform, adherent, refractory magnesium silicate coating having electrical insulating and high temperature separating properties, said process requiring depositing a film of magnesium hydroxide on the surface of the steel article and then annealing at an elevated temperature, the improvement in a method for depositing the magnesium hydroxide on the steel article comprising: immersing the steel article in a water solution having a magnesium salt concentration of from about 10 to 100 grams per liter at temperatures from about 25 to 80 C., immersing a magnesium article in said solution, and directly connecting said steel article to said magnesium article through an electrical conductor, whereby magnesium hydroxide will be deposited on the steel by galvanic action.
6. The process of applying a coating of magnesium hydroxide on an iron containing member which comprises immersing the iron containing member and a magnesium metal member directly electricallyconnected thereto in an electrolyte comprising a water solution having a concentration of above about 10 grams per liter of a salt selected from the group consisting of magnesium acetate, magnesium chloride, magnesium nitrate, and magnesium sulfate, for a sutficient time to deposit a magnesium hydroxide coating on the iron containing member by galvanic action, and recovering the thus coated iron containing member.
7. The process of applying a coating of magnesium hydroxide on an iron alloy member which comprises immersing the iron alloy member and a magnesium metal member directly electrically connected thereto in an electrolyte comprising a water solution of a salt selected from the group consisting of magnesium acetate, magnesium chloride, magnesium nitrate, and magnesium sulfate, for a sufficient time to deposit a magnesium hydroxide coating on the iron alloy member by galvanic action, said solution having a concentration of said salt of about 10 to 100 grams per liter and having a temperature of about 25 to C., and recovering the thus coated iron alloy member.
8. The process of applying a coating of magnesium hydroxide on a silicon steel member containing up to about 6% silicon which comprises immersing the silicon steel member and a magnesium metal member directly electrically connected thereto in an electrolyte comprising a water solution having a concentration of above about 10 grams per liter of a salt selected from the group consisting of magnesium acetate, magnesium chloride, magnesium nitrate, and magnesium sulfate, for a sufficient time to deposit a magnesium hydroxide coating on the silicon steel member by galvanic action, and recovering the thus coated silicon steel member.
References Cited by the Examiner UNTTED STATES PATENTS 2,200,469 ,5/40 Cox 204-56 XR 2,534,234 12/50 Cox 204-56 2,597,456 5/52 Coleman et al. 136-100 2,729,551 1/56 Cohn 204-1405 X 2,779,699 1/57 Langworthy 148-122 2,957,817 10/60 Wales 204-248 3,036,141 5/62 Goldenberg et al. 136-100 WINSTON A. DOUGLAS, Primary Examiner. 'RAY K. WINDHAM, JOHN H. MACK, Examiners.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent NO 3, 208,922 September 28 1965 James M. McQuade It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as' corrected below.
Column 3, line 27, for "cotaing" read coating column 5, line 16, for "about", first occurrence, read above lines 32 and 48, for "surface", each occurrence, read surfaces Signed and sealed this 19th day of April 1966.
(SEAL) Attest:
ERNEST w. SWIDER EDWARD J. BRENNER Attesn'ng Officer Commissioner of Patents:
Claims (1)
1. THE PROCESS COMPRISING ARRANGING AN IRON ALLOY MEMBER AND A MAGNESIUM METAL MEMBER DIRECTLY ELECTRICALLY CONNECTED TO EACH OTHER IN A WATER SOLUTION HAVING A CONCENTRATION OF ABOVE ABOUT 10 GRAMS PER LITER OF A MAGNESIUM SALT FOR SUFFICIENT TIME TO DEPOSIT A MAGNESIUM HYDROXIDE COATING ON THE IRON ALLOY MEMBER BY GALVANIC ACTION, AND RECOVERING THE THUS COATED IRON ALLOY MEMBER.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US108723A US3208922A (en) | 1961-05-09 | 1961-05-09 | Galvanic process for coating iron alloys with magnesium hydroxide |
GB15744/62A GB956730A (en) | 1961-05-09 | 1962-04-25 | Improvements in process for coating iron alloys |
DEG34928A DE1242428B (en) | 1961-05-09 | 1962-05-08 | Process for the electrolytic production of a magnesium hydroxide coating on iron alloys |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US108723A US3208922A (en) | 1961-05-09 | 1961-05-09 | Galvanic process for coating iron alloys with magnesium hydroxide |
Publications (1)
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US3208922A true US3208922A (en) | 1965-09-28 |
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US108723A Expired - Lifetime US3208922A (en) | 1961-05-09 | 1961-05-09 | Galvanic process for coating iron alloys with magnesium hydroxide |
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US (1) | US3208922A (en) |
DE (1) | DE1242428B (en) |
GB (1) | GB956730A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475297A (en) * | 1966-08-08 | 1969-10-28 | Gen Electric | Method of making battery separators |
WO1995012012A1 (en) * | 1993-10-25 | 1995-05-04 | Institut National Polytechnique De Toulouse (I.N.P.T.) | Process for fabricating a refractory coating on a metal substrate |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2200469A (en) * | 1939-11-08 | 1940-05-14 | Cox George Chandler | Anticorrosive and antifouling coating and method of application |
US2534234A (en) * | 1948-02-20 | 1950-12-19 | George C Cox | Electrocoating method |
US2597456A (en) * | 1948-11-20 | 1952-05-20 | Burgess Battery Co | Primary cell |
US2729551A (en) * | 1954-01-18 | 1956-01-03 | Samuel L Cohn | Surface treatment of aluminum and its alloys |
US2779699A (en) * | 1953-10-07 | 1957-01-29 | William P Langworthy | Annealing process for magnetic material |
US2957817A (en) * | 1958-03-31 | 1960-10-25 | Gen Electric | Silverware buckets for automatic dishwashers |
US3036141A (en) * | 1956-12-18 | 1962-05-22 | Goldenberg Leo | Magnesium galvanic cell |
-
1961
- 1961-05-09 US US108723A patent/US3208922A/en not_active Expired - Lifetime
-
1962
- 1962-04-25 GB GB15744/62A patent/GB956730A/en not_active Expired
- 1962-05-08 DE DEG34928A patent/DE1242428B/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2200469A (en) * | 1939-11-08 | 1940-05-14 | Cox George Chandler | Anticorrosive and antifouling coating and method of application |
US2534234A (en) * | 1948-02-20 | 1950-12-19 | George C Cox | Electrocoating method |
US2597456A (en) * | 1948-11-20 | 1952-05-20 | Burgess Battery Co | Primary cell |
US2779699A (en) * | 1953-10-07 | 1957-01-29 | William P Langworthy | Annealing process for magnetic material |
US2729551A (en) * | 1954-01-18 | 1956-01-03 | Samuel L Cohn | Surface treatment of aluminum and its alloys |
US3036141A (en) * | 1956-12-18 | 1962-05-22 | Goldenberg Leo | Magnesium galvanic cell |
US2957817A (en) * | 1958-03-31 | 1960-10-25 | Gen Electric | Silverware buckets for automatic dishwashers |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475297A (en) * | 1966-08-08 | 1969-10-28 | Gen Electric | Method of making battery separators |
WO1995012012A1 (en) * | 1993-10-25 | 1995-05-04 | Institut National Polytechnique De Toulouse (I.N.P.T.) | Process for fabricating a refractory coating on a metal substrate |
FR2711575A1 (en) * | 1993-10-25 | 1995-05-05 | Toulouse Inst Nat Polytech | Process for producing a refractory coating on a metal substrate |
Also Published As
Publication number | Publication date |
---|---|
GB956730A (en) | 1964-04-29 |
DE1242428B (en) | 1967-06-15 |
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