US2722491A - Insulating coating - Google Patents
Insulating coating Download PDFInfo
- Publication number
- US2722491A US2722491A US255146A US25514651A US2722491A US 2722491 A US2722491 A US 2722491A US 255146 A US255146 A US 255146A US 25514651 A US25514651 A US 25514651A US 2722491 A US2722491 A US 2722491A
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- aluminum
- coating
- percent
- aluminum hydroxide
- hydroxide
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/10—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances metallic oxides
Definitions
- This invention relates to insulating coatings for condoctors and more particularly to such a coating of alumina in a binder containing both aluminum nitrate and aluminum hydroxide.
- a heater wire for an indirectly heated cathode inan electron or gaseous discharge tube with a layer of insulating material.
- One such coating in common use is made largely of alumina suspended in a binder of aluminum nitrate, methanol and water. While such a coating is satisfactory for use in, for example, home receiver tubes, there are certain other uses Where the tubes are exposed to unusual vibrations and shock. Under such use the aluminum nitrate coating does not adhere sufliciently to the wire of the heater, and breaks in use to short. the heater to the cathode, thus making the tube useless.
- alumina of. an average particle size of four microns, or less in a binder including aluminum hydroxide. as. well as aluminum nitrate.
- the binder for such a coating is made in one of two ways.
- aluminum nitrate is reacted with ammoniumhydroxide to. produce aluminum hydroxide as a. precipitate.
- WhlClllS. separated out and reacted with an insufiicient amount of nitric acid to: completely neutralize the aluminum.
- hydroxide to give a mixture of aluminum hydroxide and aluminum nitrate which, with added water andmethanol, forms the binder.
- alumina of an average particle size of four microns, or less is added to this binder prepared by either of these methods. This forms a smooth adhering coating for the conductor. This coating, when applied and baked, presents a smooth, silky finish such that a filament wire coated with it may be inserted into a cathode sleeve with considerably greater ease than the old coating of the aluminum nitrate type.
- coatings A and B The presence of the aluminum hydroxide in the binder causes the coating to adhere considerably more firmly to the conductor than coatings containing only aluminum nitrate.
- coatings A and B two representative aluminum nitrate coatings, hereinafter referred to as coatings A and B, the following results were obtained. It required eighty grams of pull on a razor blade to strip a coating of the A type from a conductor, and 160 to 200 grams of pull to strip a coating of B type, while it required 230 grams of pull to strip a coating made according to the present invention.
- the coating of this invention also exhibits considerably greater resistance to crushing than the older type coatings. In the test referred to above, it required 1,530 grams of steadily applied load to crush a span of A coating one-eighth inch in width between two jaws. It required 2,940 to 3,360 grams to crush such a span of B coating, but it required 5,800 grams to crush such a span of the coating of the present invention.
- a characteristic batch of the binder of the invention is prepared from 481 grams of aluminum nitrate dissolved inv two liters of distilled water. 200 milliliters of ammonium hydroxide, NH4OH, of reagent grade containing 29.2 per cent. of ammonia (NH3), and having a specific gravity of 0.89, isadded slowly to this solution. Additional amounts of ammonium hydroxide are added in increments of about ten milliliters until the odor of ammonia gas is detected, indicating that the aluminum hydroxide produced by the reaction has been completely precipitated. With the quantities given, 253 milliliters of the ammonium hydroxide would be required to completely convert the aluminum nitrate.
- the mixture is heated, preferably in. a steam bath, for several hours with occasional stirring until the interaction is complete.
- the resulting milky opalescent. solution is cooled to about 25 degrees centigrade and water. added, if necessary, to give the solution a specific gravity of 1.16 and a pH- value of 2.75 to 2.85. Additional acid may be needed. to attain this range of pH values..
- the resulting binder comprises:
- This binder can be produced by the alternative process described below.
- a representative batch 212 grams of aluminum nitrate, Al(NO3)3'9H2O, are dissolved in 100 milliliters of distilled water and about 120 milliliters of ammonium hydroxide, NH4OH, added to react with the aluminum nitrate to produce aluminum hydroxide by the same process as above.
- the precipitated wet aluminum hydroxide is filtered from the solution and dried, preferably by suction.
- 750 grams of aluminum nitrate, Al(NO3)s-9H2O, and one liter of water are added to the mixture which is then heated to about to degrees centigrade.
- the aluminum hydroxide dissolves partially in the natural acidity of the aluminum nitrate salt to form a semi-colloidal material that is the same as the binder produced by the first method and has the same composition, specific gravity and pH.
- alumina, A1203, of an average particle size of not more than four microns is added to produce a mixture of the following composition:
- the coating mixture When the coating mixture is applied to the conductor and baked, the methanol and most of the water evaporate. During the baking at a temperature between 550 degrees centigrade and 850 degrees centigrade, the aluminum nitrate breaks up into aluminum oxide and nitrogen trioxide. The aluminum hydroxide also breaks up into aluminum oxide and water.
- alumina is not freely soluble in water while the nitrate is, and the hydroxide forms a colloidal suspension.
- a salt must be used that does not break down into a by-product in addition to alumina that has a deleterious effect on the tube components. Chlorides and sulphates would give by-products on baking that would have such deleterious effects.
- An insulating coating composition for a conductor consisting of approximately sixty-two percent by weight of alumina in approximately thirty-eight percent by weight of a binder consisting essentially of aluminum nitrate, aluminum hydroxide, methanol and water.
- An insulating coating composition for a conductor consisting of approximately sixty-two percent by weight of alumina with approximately thirty-eight percent of a binder consisting of twenty percent aluminum nitrate, two percent aluminum hydroxide, sixty percent water, and eighteen percent methanol.
- a binder for an insulating coating for conductors consisting of twenty percent aluminum nitrate, two percent aluminum hydroxide, sixty percent water and eighteen percent methanol, all by weight.
- the improvement which consists of coating the conductor with a suspension of alumina in a binder of twenty percent by weight of aluminum nitrate, two percent aluminum hydroxide, sixty percent water and eighteen percent methanol, heating to a temperature of between 550 and 850 degrees centigrade to adhere the aluminum compounds to the conductor and to themselves and cooling to room temperature.
- Alumina 89 Aluminum nitrate 10
- Aluminum hydroxide 1 heating to a temperature of between 550 and 850 degrees centigrade to adhere the aluminum compounds to the conductor and to themselves and cooling to room temperature.
- the improvement which consists of reacting aluminum nitrate with ammonium hydroxide to produce aluminum hydroxide, reacting the aluminum hydroxide with twenty-two percent by weight less than the amount of nitric acid necessary to neutralize the aluminum hydroxide to produce a mixture of one part by weight of aluminum hydroxide to ten parts of aluminum nitrate and adding enough water and methanol to produce a mixture of ten parts of aluminum nitrate, one part of aluminum hydroxide, thirty parts of water, and nine parts of methanol.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
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- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Description
United States Patent INSULATING COATING Mauritz L. Anderson, Arlington, Mass., assignor to Raytheon Manufacturing Company, Newton, Mass., a corporation of Delaware 7 Claims. (Cl. 117--231) This invention relates to insulating coatings for condoctors and more particularly to such a coating of alumina in a binder containing both aluminum nitrate and aluminum hydroxide.
It is customary to coat a heater wire for an indirectly heated cathode inan electron or gaseous discharge tube with a layer of insulating material. One such coating in common use is made largely of alumina suspended in a binder of aluminum nitrate, methanol and water. While such a coating is satisfactory for use in, for example, home receiver tubes, there are certain other uses Where the tubes are exposed to unusual vibrations and shock. Under such use the aluminum nitrate coating does not adhere sufliciently to the wire of the heater, and breaks in use to short. the heater to the cathode, thus making the tube useless.
It has also been found desirable to. have as smooth a finish as possible on the outer surface of the coated conductor for ease in inserting the heater into the cathode sleeve. It is also desirable to expose as little as possible of the conductor when the coated wire is folded to form a heater, for instance.
it has been found that these desirable qualities are obtained in greater degree in the coating of the present invention comprising alumina of. an average particle size of four microns, or less, in a binder including aluminum hydroxide. as. well as aluminum nitrate.
The binder for such a coating is made in one of two ways. By the first method, aluminum nitrate is reacted with ammoniumhydroxide to. produce aluminum hydroxide as a. precipitate. WhlClllS. separated out and reacted with an insufiicient amount of nitric acid to: completely neutralize the aluminum. hydroxide to give a mixture of aluminum hydroxide and aluminum nitrate which, with added water andmethanol, forms the binder.
By the second method: of making thebinder, aluminum nitrate is reacted with. sufiicient ammonium. hydroxide to produce the amount of aluminum hydroxide that it is desired to have in the finished batch of binder. To' this the desired quantity of aluminum nitrate is added.
To this binder prepared by either of these methods, alumina of an average particle size of four microns, or less, is added. This forms a smooth adhering coating for the conductor. This coating, when applied and baked, presents a smooth, silky finish such that a filament wire coated with it may be inserted into a cathode sleeve with considerably greater ease than the old coating of the aluminum nitrate type.
The presence of the aluminum hydroxide in the binder causes the coating to adhere considerably more firmly to the conductor than coatings containing only aluminum nitrate. In comparative tests with two representative aluminum nitrate coatings, hereinafter referred to as coatings A and B, the following results were obtained. It required eighty grams of pull on a razor blade to strip a coating of the A type from a conductor, and 160 to 200 grams of pull to strip a coating of B type, while it required 230 grams of pull to strip a coating made according to the present invention.
The coating of this invention also exhibits considerably greater resistance to crushing than the older type coatings. In the test referred to above, it required 1,530 grams of steadily applied load to crush a span of A coating one-eighth inch in width between two jaws. It required 2,940 to 3,360 grams to crush such a span of B coating, but it required 5,800 grams to crush such a span of the coating of the present invention.
A characteristic batch of the binder of the invention is prepared from 481 grams of aluminum nitrate dissolved inv two liters of distilled water. 200 milliliters of ammonium hydroxide, NH4OH, of reagent grade containing 29.2 per cent. of ammonia (NH3), and having a specific gravity of 0.89, isadded slowly to this solution. Additional amounts of ammonium hydroxide are added in increments of about ten milliliters until the odor of ammonia gas is detected, indicating that the aluminum hydroxide produced by the reaction has been completely precipitated. With the quantities given, 253 milliliters of the ammonium hydroxide would be required to completely convert the aluminum nitrate. However, a slight excess is desirable so that a total of 260 to 265 milliliters of ammonium hydroxide should be added to this batch to produce 100 grams of dry aluminum hydroxide. The precipitated aluminum hydroxide is in a moist state. The quantities indicated produce 750 grams of moist aluminum hydroxide.
345 grams of nitric acid of per cent. purity would be required to completely neutralize 100 grams of aluminum hydroxide. This is equivalent to 243 milliliters of acid. However, as it is only desiredv to convert 78 per cent. of the hydroxide to aluminum nitrate leaving 22 per cent. of the original quantity as aluminum hydroxide, only 190 milliliters of acid are required.
After the acid is added, the mixture is heated, preferably in. a steam bath, for several hours with occasional stirring until the interaction is complete. The resulting milky opalescent. solution is cooled to about 25 degrees centigrade and water. added, if necessary, to give the solution a specific gravity of 1.16 and a pH- value of 2.75 to 2.85. Additional acid may be needed. to attain this range of pH values..
The resulting binder comprises:
Percent by weight This binder can be produced by the alternative process described below. In a representative batch 212 grams of aluminum nitrate, Al(NO3)3'9H2O, are dissolved in 100 milliliters of distilled water and about 120 milliliters of ammonium hydroxide, NH4OH, added to react with the aluminum nitrate to produce aluminum hydroxide by the same process as above. The precipitated wet aluminum hydroxide is filtered from the solution and dried, preferably by suction. To the resulting wet cake, 750 grams of aluminum nitrate, Al(NO3)s-9H2O, and one liter of water are added to the mixture which is then heated to about to degrees centigrade. The aluminum hydroxide dissolves partially in the natural acidity of the aluminum nitrate salt to form a semi-colloidal material that is the same as the binder produced by the first method and has the same composition, specific gravity and pH.
One volume of methanol, (CI-IaOH), is added to three volumes of the solution to produce the final binder comprising:
Percent by weight Aluminum nitrate 18.47 Aluminum hydroxide 1.88 Water 61.37 Methanol 18.28
To produce the desired coating, sufficient alumina, A1203, of an average particle size of not more than four microns is added to produce a mixture of the following composition:
Percent by weight Alumina 61.77 Aluminum nitrate 7.06 Aluminum hydroxide 0.72 Water 23.46 Methanol 6.99
In production, it is frequently found that it is easier to apply the coating if it is made somewhat thinner than indicated above. However, if more than 20 percent by volume of liquids is added, the result will be too thin to be effective.
When the coating mixture is applied to the conductor and baked, the methanol and most of the water evaporate. During the baking at a temperature between 550 degrees centigrade and 850 degrees centigrade, the aluminum nitrate breaks up into aluminum oxide and nitrogen trioxide. The aluminum hydroxide also breaks up into aluminum oxide and water.
The reason for using aluminum nitrate and aluminum hydroxide instead of only alumina is that alumina is not freely soluble in water while the nitrate is, and the hydroxide forms a colloidal suspension. Another consideration is that a salt must be used that does not break down into a by-product in addition to alumina that has a deleterious effect on the tube components. Chlorides and sulphates would give by-products on baking that would have such deleterious effects.
What is claimed is:
1. An insulating coating composition for a conductor consisting of approximately sixty-two percent by weight of alumina in approximately thirty-eight percent by weight of a binder consisting essentially of aluminum nitrate, aluminum hydroxide, methanol and water.
2. An insulating coating composition for a conductor consisting of approximately sixty-two percent by weight of alumina with approximately thirty-eight percent of a binder consisting of twenty percent aluminum nitrate, two percent aluminum hydroxide, sixty percent water, and eighteen percent methanol.
3. A binder for an insulating coating for conductors consisting of twenty percent aluminum nitrate, two percent aluminum hydroxide, sixty percent water and eighteen percent methanol, all by weight.
4. In the process of producing an insulated electrical conductor, the improvement which consists of coating the conductor with a suspension of alumina in a binder of twenty percent by weight of aluminum nitrate, two percent aluminum hydroxide, sixty percent water and eighteen percent methanol, heating to a temperature of between 550 and 850 degrees centigrade to adhere the aluminum compounds to the conductor and to themselves and cooling to room temperature.
5. In the process of producing an insulated electrical conductor, the improvement which consists of coating a conductor with an aqueous and methanol suspension of alumina compounds in the following proportions:
Percent by weight Alumina 89 Aluminum nitrate 10 Aluminum hydroxide 1 heating to a temperature of between 550 and 850 degrees centigrade to adhere the aluminum compounds to the conductor and to themselves and cooling to room temperature.
6. In the process of producing a binder for an insulating coating of alumina, the improvement which consists of reacting aluminum nitrate with ammonium hydroxide to produce aluminum hydroxide, reacting the aluminum hydroxide with twenty-two percent by weight less than the amount of nitric acid necessary to neutralize the aluminum hydroxide to produce a mixture of one part by weight of aluminum hydroxide to ten parts of aluminum nitrate and adding enough water and methanol to produce a mixture of ten parts of aluminum nitrate, one part of aluminum hydroxide, thirty parts of water, and nine parts of methanol.
7. In the process of producing a binder for an insulating coating the improvement which consists of the steps of dissolving aluminum nitrate in water, adding ammonium hydroxide to produce aluminum hydroxide and ammonium nitrate, reacting the aluminum hydroxide with twentytwo percent by weight less nitric acid than is sutficient to neutralize all the aluminum hydroxide to produce a mixture of one part by weight of aluminum hydroxide to ten parts of aluminum nitrate and adding enough water and methanol to produce a mixture of ten parts of aluminum nitrate, one part of aluminum hydroxide, thirty parts of water and nine parts of methanol and having a specific gravity of 1.16 and a pH value of between 2.75 and 2.85
References Cited in the file of this patent UNITED STATES PATENTS 2,307,018 Cardell Ian. 5, 1943 2,530,546 Snyder Nov. 21, 1950 2,635,995 Swanson Apr. 4, 1953 FOREIGN PATENTS 987,628 France Aug. 16, 1951 OTHER REFERENCES Hackhs Chemical Dictionary, 2nd ed., 1937, pp. 237- 238.
Claims (1)
1. AN INSULATING COATING COMPOSITION FOR A CONDUCTOR CONSISTING OF APPROXIMATELY SIXTY-TWO PERCENT BY WEIGHT OF ALUMINA IN APPROXIMATELY THIRTY-EIGHT PERCENT BY WEIGHT OF A BINDER CONSISTING ESSENTIALLY OF ALUMINUM NITRATE, ALUMINUM HYDROXIDE, METHANOL AND WATER.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US255146A US2722491A (en) | 1951-11-06 | 1951-11-06 | Insulating coating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US255146A US2722491A (en) | 1951-11-06 | 1951-11-06 | Insulating coating |
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US2722491A true US2722491A (en) | 1955-11-01 |
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US255146A Expired - Lifetime US2722491A (en) | 1951-11-06 | 1951-11-06 | Insulating coating |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2890971A (en) * | 1956-05-02 | 1959-06-16 | Rca Corp | Coating method |
US3221203A (en) * | 1962-06-01 | 1965-11-30 | Rca Corp | Sintered metal conductor support |
US3427195A (en) * | 1964-04-20 | 1969-02-11 | Condensateurs Sic Safco Sa | Electrode for electrolytic condenser and process for producing the same |
US4146665A (en) * | 1971-12-03 | 1979-03-27 | Owens-Illinois, Inc. | Gas discharge device containing coated dielectric |
US4566173A (en) * | 1981-06-05 | 1986-01-28 | International Business Machines Corporation | Gate insulation layer and method of producing such a structure |
US4731560A (en) * | 1970-08-06 | 1988-03-15 | Owens-Illinois Television Products, Inc. | Multiple gaseous discharge display/memory panel having improved operating life |
US4794308A (en) * | 1970-08-06 | 1988-12-27 | Owens-Illinois Television Products Inc. | Multiple gaseous discharge display/memory panel having improved operating life |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2307018A (en) * | 1938-06-25 | 1943-01-05 | Raytheon Production Corp | Cataphoretic deposition of insulating coatings |
US2530546A (en) * | 1946-06-08 | 1950-11-21 | Bell Telephone Labor Inc | Electrophoretic deposition of insulating coating |
FR987628A (en) * | 1948-06-19 | 1951-08-16 | Rca Corp | Insulating plaster material |
US2635995A (en) * | 1948-06-19 | 1953-04-21 | Rca Corp | Electrophoretic insulating coating |
-
1951
- 1951-11-06 US US255146A patent/US2722491A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2307018A (en) * | 1938-06-25 | 1943-01-05 | Raytheon Production Corp | Cataphoretic deposition of insulating coatings |
US2530546A (en) * | 1946-06-08 | 1950-11-21 | Bell Telephone Labor Inc | Electrophoretic deposition of insulating coating |
FR987628A (en) * | 1948-06-19 | 1951-08-16 | Rca Corp | Insulating plaster material |
US2635995A (en) * | 1948-06-19 | 1953-04-21 | Rca Corp | Electrophoretic insulating coating |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2890971A (en) * | 1956-05-02 | 1959-06-16 | Rca Corp | Coating method |
US3221203A (en) * | 1962-06-01 | 1965-11-30 | Rca Corp | Sintered metal conductor support |
US3427195A (en) * | 1964-04-20 | 1969-02-11 | Condensateurs Sic Safco Sa | Electrode for electrolytic condenser and process for producing the same |
US4731560A (en) * | 1970-08-06 | 1988-03-15 | Owens-Illinois Television Products, Inc. | Multiple gaseous discharge display/memory panel having improved operating life |
US4794308A (en) * | 1970-08-06 | 1988-12-27 | Owens-Illinois Television Products Inc. | Multiple gaseous discharge display/memory panel having improved operating life |
US4146665A (en) * | 1971-12-03 | 1979-03-27 | Owens-Illinois, Inc. | Gas discharge device containing coated dielectric |
US4566173A (en) * | 1981-06-05 | 1986-01-28 | International Business Machines Corporation | Gate insulation layer and method of producing such a structure |
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