US2745932A - Electric resistor - Google Patents
Electric resistor Download PDFInfo
- Publication number
- US2745932A US2745932A US359345A US35934553A US2745932A US 2745932 A US2745932 A US 2745932A US 359345 A US359345 A US 359345A US 35934553 A US35934553 A US 35934553A US 2745932 A US2745932 A US 2745932A
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- US
- United States
- Prior art keywords
- mosiz
- heater
- molybdenum disilicide
- graphite
- molybdenum
- Prior art date
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- 238000002844 melting Methods 0.000 claims description 16
- 230000008018 melting Effects 0.000 claims description 16
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims description 7
- 239000011733 molybdenum Substances 0.000 claims description 7
- 239000003575 carbonaceous material Substances 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 5
- 238000005485 electric heating Methods 0.000 claims description 2
- YXTPWUNVHCYOSP-UHFFFAOYSA-N bis($l^{2}-silanylidene)molybdenum Chemical compound [Si]=[Mo]=[Si] YXTPWUNVHCYOSP-UHFFFAOYSA-N 0.000 description 27
- 229910021343 molybdenum disilicide Inorganic materials 0.000 description 27
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 24
- 229910002804 graphite Inorganic materials 0.000 description 24
- 239000010439 graphite Substances 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 239000010410 layer Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000011247 coating layer Substances 0.000 description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 6
- 229910010271 silicon carbide Inorganic materials 0.000 description 6
- 239000002344 surface layer Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 229910017305 Mo—Si Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910016006 MoSi Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 1
- 229910000951 Aluminide Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910020968 MoSi2 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
- 229910003452 thorium oxide Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/04—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of carbon-silicon compounds, carbon or silicon
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
- H05B3/12—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
- H05B3/14—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
- H05B3/148—Silicon, e.g. silicon carbide, magnesium silicide, heating transistors or diodes
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B2203/00—Aspects relating to Ohmic resistive heating covered by group H05B3/00
- H05B2203/018—Heaters using heating elements comprising mosi2
Definitions
- This invention relates to electric resistor heater bodies, and more particularly to such bodies which are formed with molybdenum disilicide, and to the production of such heater bodies.
- molybdenum disilicide MOSiz has unusually desirable properties which would make it an ideal material for electric resistor heater bodies.
- electrical heater rod bodies for electric furnaces and the like have as a rule, been made out .of silicon carbide cemented with nickel carbide, such heater bodies being known commercially as globar bodies.
- the known silicon carbide heater bodies have a maximum operating temperature of about 1400 C., and they are made with a resistivity of 2000 to 5000 microhm centimeters because with lower resistivity it is difiicult to supply such heater bodies with the much larger currents that would be required to bring them to the desired high operating temperatures.
- molybdenum disilicide Because of its relatively low electrical resistivity of about 22 microhm centimeters at room temperatures, no practical way was found in the past for utilizing molybdenum disilicide as electrical heater bodies. Cemented bodies of molybdenum disilicide are very brittle and fragile and proposals to increase the resistivity of molybdenum disilicide by additions of molybdenum aluminides, and/or melting oxides, such as zirconium oxide, thorium oxide which become conducting at high tempera- .tures, and/or other high melting oxides, such as aluminum oxide, beryllium oxide, silicon oxide, likewise failed because these additions result in a further increase of the objectionable brittleness of molybdenum disilicide.
- molybdenum aluminides, and/or melting oxides such as zirconium oxide, thorium oxide which become conducting at high tempera- .tures, and/or other high melting oxides, such as aluminum oxide, beryllium oxide,
- a superior electric heater body may be formed by providing a body such as a rod of graphite or similar material with a surface layer of molybdenum disilicide and heating the combined body to a high temperature at which the surface layer of molybdenum disilicide is liquefied and combined with the surface strata of the graphite body into a composite surface layer which has a melting point of about 2450 C. or higher and resists corrosion in oxidizing atmospheres at temperatures up to 1900 C. and higher.
- Bodies of pure molybdenum disilicide MoSiz which melts at about 1880 C. can be readily molded from MOSiz powders by powder metallurgy and ceramic techniques. Because of their high stability and resistance to corrosion in oxidizing atmospheres at 1700 to 1800 C., many proposals have been made in the past for using cemented MOSiz material in electric resistance heaters for operation at heating temperatures of about 1700 C.
- heater bodies of this material would have to be made with a very thin cross-section, such as thin tubing or ribbon, and even with such thin cross-section, they would be impractical as electrical heater bodies because of the dificulties of supplying them with relatively large currents which would be required to maintain them at the desired high temperature.
- Coated heater body The present invention is based on the discovery that a novel electric heater body of desired characteristics will be formed by coating a heater body such as a heater rod of graphite or like material with a surface layer of molybdenum disilicide MOSiz and heating the combined coated body to a high temperature at which the surface layer of molybdenum disilicide MoSiz is liquefied and combined with the surface strata of the graphite body into a composite surface layer formation which has a melting point in excess of 2450 C. and thereby providing a heater body which may be operated for a long period without corrosion at temperatures in excess of l700 in oxidizing atmospheres.
- a heater body such as a heater rod of graphite or like material
- MOSiz molybdenum disilicide MOSiz
- molybdenum disilicide MOSiz is applied in the form of a coating to a heater body or rod of a material such as graphite and the so-coated body is heated in an inert atmosphere to a high temperature above the melting temperature of molybdenum disilicide MOSiz which is about 1880".
- the molybdenum disilicide MOSiz powder may be applied to the red by mixing it with a suspension liquid and spraying or otherwise applying the powder suspension to the surface of the rod.
- the so-coated body is heated in an inert atmosphere, such as argon at temperatures above the melting temperature of molybdenum disilicide MoSiz, such as 2250 C.
- molybdenum disilicide MoSi: powder When a heater rod of graphite coated with a layer of molybdenum disilicide MoSi: powder, is heated in an inert atmosphere to temperatures between 2200 C. the liquified molybdenum disilicide IVIOSiz decomposes and carbonizes and combines with the adjacent strata of the graphite rod and forms with it a composite surface coating having a melting temperature in excess of 2450 C.
- the surface formation so obtained consists essentially of MoSi double carbide which resists oxidation at temperatures up to about 2200 C. and higher, and it remains stable at these temperatures and has a considerably higher resistivity than molybdenum disilicide MoSiz.
- the combined MtF-Si double carbide has about 300 to 500 microhm centimeter resistivity compared to 22 microhm centimeter resistivity of molybdenum disilicide MoSiz.
- This Mo-Si double carbide material has desirable characteristics in that its thermal coefficient of resistance remains substantially zero over the temperature range from about 1200 C. up to 1900" C. and higher up to below its melting temperature.
- the thickness of the double carbide coating of the invention so formed may be readily controlled by controlling the thickness of the molybdenum disilicide MoSi2 coating layer applied to the graphite rod, and such coating formation suflicient thickness as to cause the double carbide coating layer to form a continuous and dense tightly adhering coating formation which prevents corrosion or deterioration of the underlying strata of the graphite rod when the combined heater body is operated at temperatures of 1700 C. to 1900 C. within oxidizing atmospheres.
- the graphite rods which are so provided with a double carbide coating of the invention need not have such coating at their contact ends because these contact ends are usually combined and covered with water cooled copper electrodes which maintain the contact ends at lower temperatures at which the so covered graphite is not oxidized. Accordingly, the graphite rods which have already mounted thereon the Water cooled metallic contact terminal sleeves, may be coated along the exposed parts of the graphite rod with the Mo--Si double carbide coating of the invention.
- the exposed graphite rod is coated with a layer of molybdenum disilicide MOSiz and the so-coated graphite rod is heated by sending heating current through the graphite rod for raising its temperature to above the melting temperature of molybdenum disilicide MoSiz, to wit, to about 2200 to 2300 C. while maintaining it in an atmosphere of argon or like insert gas until the double carbide formation is formed on the surface of the graphite rod in the manner explained above.
- the double carbide coating may be readily formed so as to have uniform thickness since the liquefied molybdenum disilicide MoSiz may be readily allowed to run freely around the rod during the heating stage at which the molybdenum disilicide MoSig coating remains in molten condition.
- the process of the invention of the type described may be repeated with successive strata of molybdenum disilicide MoSiz placed on the graphite rod and subjected to the treatment described above for converting the exterior of the graphite rod into a comi posite Mo--Si double carbide layer having great corrosion-resistance and a melting temperature of 2400 C., and a thickness which will assure protection of the underlying body of the graphite rod against corrosion at temperatures of 1700 to 2200 C.
- the drawing shows a heater body exemplifying this form of the invention.
- a rod 21 of graphite is provided at its ends with water coated metal terminals 22.
- the exposed surface of the graphite rod is covered with a coating layer 23 of molybdenum disilicide MoSiz Whereupon the graphite rod 21 is subjected to a treatment wherein the exterior is converted into an adherent corrosion resistant Mo-Si double carbide coating layer.
- Heaters of the invention formed in the manner described above are superior to conventional silicon carbide heaters because they may be operated for prolonged periods of time without corrosion at temperatures much higher than the maximum temperature of 1400 at which such silicon carbide heaters may be used, the heaters of the invention cost only a fraction of the cost of such silicon carbide heaters.
- a solid elongated heater body of substantial thickness arranged to be traversed by electric heating current and consisting of carbonaceous material, said body having metal electrodes at opposite end regions, the entire exposed surface of said heater body between said end regions having as an integral part thereof a dense continuous enclosure layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C.
- said enclosure layer being of substantially uniform thickness of between about 0.003 to 0.006 inch.
- a solid elongated heater body of substantial thickness arranged to be traversed by electric current and consisting of carbonaceous material, said heater body having metal electrodes at opposite end regions, the entire exposed surface of said heater body between said end regions having as an integral part thereof a dense continuous enclosure layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C. which enclosure layer has been formed by uniting MOSiz portions to said entire exposed surface of said heater body and heating said united MoSiz portions in an inert atmosphere at a temperature of at least 1800 C. and above the melting temperature of MOSiz to cause said MoSiz portions to liquefy, decompose and combine with underlying strata of said carbonaceous material into said double carbide of molybdenum and silicon of said enclosure layer.
- an electric heater device comprising providing a solid elongated body of substantial thickness consisting of carbonaceous material having metal electrodes at opposite end regions, uniting MoSiz portions to the entire exposed surface of said body extending between said electrode regions, heating said united MoSiz portions in an inert atmosphere at a temperature of at least 1800 C. and causing said MOSiz portions to melt, decompose and combine with the adjacent underlying strata of said carbonaceous body into a continuous enclosure layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C. and enclosing the entire exposedsurface of said elongated body.
- an electric heater device comprising providing a solid elongated body of substantial thickness consisting of carbonaceous material having metal electrodes at opposite end regions, applying to the entire exposed surface of said body extending between said electrode regions a continuous coating of molybdenum disilicide MoSiz, maintaining said body in an inert atmosphere, passing electric current through said elongated body until said coating is heated to a temperature of at least 1800 C. at which the MoSiz of said coating layer melts and decomposes and combines with the adjacent underlying strata of said carbonaceous body into a continuous layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C. and enclosing the entire exposed surface of said elongated body.
Landscapes
- Resistance Heating (AREA)
Description
y 5, 1956 F. w. GLASER 2,745,932
ELECTRIC RESISTOR Filed June 3, 1953 IN V EN TOR. 441v AM 6445,52
United States Patent ELECTRIC RESISTOR Frank W. Glaser, New York, N. Y., assignor to American Electro Metal Corporation, Yonkers, N. Y., a corpora tion of Maryland Application June 3, 1953, Serial No. 359,345 5 Claims. (Cl. 201-75) This invention relates to electric resistor heater bodies, and more particularly to such bodies which are formed with molybdenum disilicide, and to the production of such heater bodies.
It has long been known that molybdenum disilicide MOSiz has unusually desirable properties which would make it an ideal material for electric resistor heater bodies.
However, in the past, electrical heater rod bodies for electric furnaces and the like have as a rule, been made out .of silicon carbide cemented with nickel carbide, such heater bodies being known commercially as globar bodies. The known silicon carbide heater bodies have a maximum operating temperature of about 1400 C., and they are made with a resistivity of 2000 to 5000 microhm centimeters because with lower resistivity it is difiicult to supply such heater bodies with the much larger currents that would be required to bring them to the desired high operating temperatures.
Because of its relatively low electrical resistivity of about 22 microhm centimeters at room temperatures, no practical way was found in the past for utilizing molybdenum disilicide as electrical heater bodies. Cemented bodies of molybdenum disilicide are very brittle and fragile and proposals to increase the resistivity of molybdenum disilicide by additions of molybdenum aluminides, and/or melting oxides, such as zirconium oxide, thorium oxide which become conducting at high tempera- .tures, and/or other high melting oxides, such as aluminum oxide, beryllium oxide, silicon oxide, likewise failed because these additions result in a further increase of the objectionable brittleness of molybdenum disilicide.
The present invention is based on the discovery that a superior electric heater body may be formed by providing a body such as a rod of graphite or similar material with a surface layer of molybdenum disilicide and heating the combined body to a high temperature at which the surface layer of molybdenum disilicide is liquefied and combined with the surface strata of the graphite body into a composite surface layer which has a melting point of about 2450 C. or higher and resists corrosion in oxidizing atmospheres at temperatures up to 1900 C. and higher.
The foregoing and other objects of the invention will be best understood from the following description of exemplifications thereof, reference being made to the accompanying drawings, wherein the single figure is an elevational view with parts in section showing one form of heater body exemplifying the invention.
Bodies of pure molybdenum disilicide MoSiz which melts at about 1880 C. can be readily molded from MOSiz powders by powder metallurgy and ceramic techniques. Because of their high stability and resistance to corrosion in oxidizing atmospheres at 1700 to 1800 C., many proposals have been made in the past for using cemented MOSiz material in electric resistance heaters for operation at heating temperatures of about 1700 C. However, because MoSiz has a relatively low electrical resistivity of only 22 microhm centimeters at room temperature, heater bodies of this material would have to be made with a very thin cross-section, such as thin tubing or ribbon, and even with such thin cross-section, they would be impractical as electrical heater bodies because of the dificulties of supplying them with relatively large currents which would be required to maintain them at the desired high temperature.
In addition, such cemented MoSiz material is very brittle and accordingly, thin heater bodies of silicon carbide are also impractical because of their excessive critical brittleness.
Coated heater body The present invention is based on the discovery that a novel electric heater body of desired characteristics will be formed by coating a heater body such as a heater rod of graphite or like material with a surface layer of molybdenum disilicide MOSiz and heating the combined coated body to a high temperature at which the surface layer of molybdenum disilicide MoSiz is liquefied and combined with the surface strata of the graphite body into a composite surface layer formation which has a melting point in excess of 2450 C. and thereby providing a heater body which may be operated for a long period without corrosion at temperatures in excess of l700 in oxidizing atmospheres.
According to this phase of the invention, molybdenum disilicide MOSiz is applied in the form of a coating to a heater body or rod of a material such as graphite and the so-coated body is heated in an inert atmosphere to a high temperature above the melting temperature of molybdenum disilicide MOSiz which is about 1880". The molybdenum disilicide MOSiz powder may be applied to the red by mixing it with a suspension liquid and spraying or otherwise applying the powder suspension to the surface of the rod. The so-coated body is heated in an inert atmosphere, such as argon at temperatures above the melting temperature of molybdenum disilicide MoSiz, such as 2250 C. When a heater rod of graphite coated with a layer of molybdenum disilicide MoSi: powder, is heated in an inert atmosphere to temperatures between 2200 C. the liquified molybdenum disilicide IVIOSiz decomposes and carbonizes and combines with the adjacent strata of the graphite rod and forms with it a composite surface coating having a melting temperature in excess of 2450 C. The surface formation so obtained consists essentially of MoSi double carbide which resists oxidation at temperatures up to about 2200 C. and higher, and it remains stable at these temperatures and has a considerably higher resistivity than molybdenum disilicide MoSiz. Thus the combined MtF-Si double carbide has about 300 to 500 microhm centimeter resistivity compared to 22 microhm centimeter resistivity of molybdenum disilicide MoSiz. This Mo-Si double carbide material has desirable characteristics in that its thermal coefficient of resistance remains substantially zero over the temperature range from about 1200 C. up to 1900" C. and higher up to below its melting temperature.
The thickness of the double carbide coating of the invention so formed may be readily controlled by controlling the thickness of the molybdenum disilicide MoSi2 coating layer applied to the graphite rod, and such coating formation suflicient thickness as to cause the double carbide coating layer to form a continuous and dense tightly adhering coating formation which prevents corrosion or deterioration of the underlying strata of the graphite rod when the combined heater body is operated at temperatures of 1700 C. to 1900 C. within oxidizing atmospheres.
may be readily made of or built up to.
The graphite rods which are so provided with a double carbide coating of the invention need not have such coating at their contact ends because these contact ends are usually combined and covered with water cooled copper electrodes which maintain the contact ends at lower temperatures at which the so covered graphite is not oxidized. Accordingly, the graphite rods which have already mounted thereon the Water cooled metallic contact terminal sleeves, may be coated along the exposed parts of the graphite rod with the Mo--Si double carbide coating of the invention. In other Words the exposed graphite rod is coated with a layer of molybdenum disilicide MOSiz and the so-coated graphite rod is heated by sending heating current through the graphite rod for raising its temperature to above the melting temperature of molybdenum disilicide MoSiz, to wit, to about 2200 to 2300 C. while maintaining it in an atmosphere of argon or like insert gas until the double carbide formation is formed on the surface of the graphite rod in the manner explained above.
The double carbide coating may be readily formed so as to have uniform thickness since the liquefied molybdenum disilicide MoSiz may be readily allowed to run freely around the rod during the heating stage at which the molybdenum disilicide MoSig coating remains in molten condition. The process of the invention of the type described may be repeated with successive strata of molybdenum disilicide MoSiz placed on the graphite rod and subjected to the treatment described above for converting the exterior of the graphite rod into a comi posite Mo--Si double carbide layer having great corrosion-resistance and a melting temperature of 2400 C., and a thickness which will assure protection of the underlying body of the graphite rod against corrosion at temperatures of 1700 to 2200 C.
The drawing shows a heater body exemplifying this form of the invention. A rod 21 of graphite is provided at its ends with water coated metal terminals 22. The exposed surface of the graphite rod is covered with a coating layer 23 of molybdenum disilicide MoSiz Whereupon the graphite rod 21 is subjected to a treatment wherein the exterior is converted into an adherent corrosion resistant Mo-Si double carbide coating layer.
Good results are obtained with heater bodies of the type described above, wherein the coating layer 23 of the Mo-Si double carbide layer has a thickness of about .003 to .006 inch.
In forming composite heater bodies' of the invention of the type described above, it is important that the graphite of the rod shall be substantially free of sulphur.
Heaters of the invention formed in the manner described above, are superior to conventional silicon carbide heaters because they may be operated for prolonged periods of time without corrosion at temperatures much higher than the maximum temperature of 1400 at which such silicon carbide heaters may be used, the heaters of the invention cost only a fraction of the cost of such silicon carbide heaters.
The features and principles underlying the invention described above in connection with specific exemplifies.- tions, will suggest to those skilled in the art many other modifications thereof. It is accordingly desired that the appended claims be construed broadly and that they shall not be limited to the specific details shown and described in connection with exemplifications thereof.
I claim:
1. In an electric heater device, a solid elongated heater body of substantial thickness arranged to be traversed by electric heating current and consisting of carbonaceous material, said body having metal electrodes at opposite end regions, the entire exposed surface of said heater body between said end regions having as an integral part thereof a dense continuous enclosure layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C.
2. In an electric heater device, as claimed in claim 1, said enclosure layer being of substantially uniform thickness of between about 0.003 to 0.006 inch.
3. In an electric heater device, a solid elongated heater body of substantial thickness arranged to be traversed by electric current and consisting of carbonaceous material, said heater body having metal electrodes at opposite end regions, the entire exposed surface of said heater body between said end regions having as an integral part thereof a dense continuous enclosure layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C. which enclosure layer has been formed by uniting MOSiz portions to said entire exposed surface of said heater body and heating said united MoSiz portions in an inert atmosphere at a temperature of at least 1800 C. and above the melting temperature of MOSiz to cause said MoSiz portions to liquefy, decompose and combine with underlying strata of said carbonaceous material into said double carbide of molybdenum and silicon of said enclosure layer.
4. The process of forming an electric heater device, comprising providing a solid elongated body of substantial thickness consisting of carbonaceous material having metal electrodes at opposite end regions, uniting MoSiz portions to the entire exposed surface of said body extending between said electrode regions, heating said united MoSiz portions in an inert atmosphere at a temperature of at least 1800 C. and causing said MOSiz portions to melt, decompose and combine with the adjacent underlying strata of said carbonaceous body into a continuous enclosure layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C. and enclosing the entire exposedsurface of said elongated body.
5. The process of forming an electric heater device, comprising providing a solid elongated body of substantial thickness consisting of carbonaceous material having metal electrodes at opposite end regions, applying to the entire exposed surface of said body extending between said electrode regions a continuous coating of molybdenum disilicide MoSiz, maintaining said body in an inert atmosphere, passing electric current through said elongated body until said coating is heated to a temperature of at least 1800 C. at which the MoSiz of said coating layer melts and decomposes and combines with the adjacent underlying strata of said carbonaceous body into a continuous layer of a double carbide of molybdenum and silicon having a melting temperature of at least 1800 C. and enclosing the entire exposed surface of said elongated body.
References Cited in the file of this patent UNlTED STATES PATENTS
Claims (1)
1. IN AN ELECTRIC HEATER DEVICE, A SOLID ELONGATED HEATER BODY OF SUBSTANTIAL THICKNESS ARRANGED TO BE TRAVERSED BY ELECTRIC HEATING CURRENT AND CONSISTING OF CARBONACEOUS MATERIAL, SAID BODY HAVING METAL ELECTRODES AT OPPOSITE END REGIONS, THE ENTIRE EXPOSED SURFACE OF SAID HEATER BODY BETWEEN SAID END REGIONS HAVING AS AN INTEGRAL PART THEREOF A DENSE CONTINUOUS ENCLOSURE LAYER OF A DOUBLE CARBIDE OF MOLYBDENUM AND SILICON HAVING A MELTING TEMPERATURE OF AT LEAST 1800* C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US359345A US2745932A (en) | 1953-06-03 | 1953-06-03 | Electric resistor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US359345A US2745932A (en) | 1953-06-03 | 1953-06-03 | Electric resistor |
Publications (1)
Publication Number | Publication Date |
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US2745932A true US2745932A (en) | 1956-05-15 |
Family
ID=23413427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US359345A Expired - Lifetime US2745932A (en) | 1953-06-03 | 1953-06-03 | Electric resistor |
Country Status (1)
Country | Link |
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US (1) | US2745932A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2866724A (en) * | 1954-03-15 | 1958-12-30 | Continental Can Co | Coated evaporating elements and method of utilizing same |
US2866725A (en) * | 1954-03-15 | 1958-12-30 | Continental Can Co | Coated evaporating elements and method of utilizing same |
DE1100772B (en) * | 1957-02-05 | 1961-03-02 | Kanthal Ab | Flame sprayed electrical resistance |
US2978358A (en) * | 1958-03-28 | 1961-04-04 | Ivor E Campbell | Method of obtaining uniform coatings on graphite |
US2993814A (en) * | 1958-05-24 | 1961-07-25 | Foerderung Forschung Gmbh | Heating conductor and method of making the same |
US3092681A (en) * | 1958-09-22 | 1963-06-04 | Kanthal Ab | Electric resistance furnaces and the like |
US3120453A (en) * | 1957-11-22 | 1964-02-04 | Siemens Planiawerke Ag | Porous carbonaceous body with sealed surface for use as arc-furnace electrode or structural component of nuclear reactors |
US3121154A (en) * | 1959-10-30 | 1964-02-11 | Babcock & Wilcox Ltd | Electric heaters |
US3171871A (en) * | 1960-07-19 | 1965-03-02 | Norton Co | Method of making electrical heater bars |
US3271181A (en) * | 1963-05-29 | 1966-09-06 | Robert A Jewell | Method of coating carbonaceous base to prevent oxidation destruction and coated base |
US3328201A (en) * | 1964-04-27 | 1967-06-27 | Rca Corp | Heater for electron tubes |
US3337375A (en) * | 1964-04-13 | 1967-08-22 | Sprague Electric Co | Semiconductor method and device |
US20200113020A1 (en) * | 2018-10-05 | 2020-04-09 | Serendipity Technologies Llc | Low power high-efficiency heating element |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1134788A (en) * | 1914-09-18 | 1915-04-06 | Gen Electric | Electric terminal. |
US2597964A (en) * | 1951-11-09 | 1952-05-27 | Union Carbide & Carbon Corp | Fluid impervious carbon article and method of making same |
-
1953
- 1953-06-03 US US359345A patent/US2745932A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1134788A (en) * | 1914-09-18 | 1915-04-06 | Gen Electric | Electric terminal. |
US2597964A (en) * | 1951-11-09 | 1952-05-27 | Union Carbide & Carbon Corp | Fluid impervious carbon article and method of making same |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2866725A (en) * | 1954-03-15 | 1958-12-30 | Continental Can Co | Coated evaporating elements and method of utilizing same |
US2866724A (en) * | 1954-03-15 | 1958-12-30 | Continental Can Co | Coated evaporating elements and method of utilizing same |
DE1100772B (en) * | 1957-02-05 | 1961-03-02 | Kanthal Ab | Flame sprayed electrical resistance |
US3120453A (en) * | 1957-11-22 | 1964-02-04 | Siemens Planiawerke Ag | Porous carbonaceous body with sealed surface for use as arc-furnace electrode or structural component of nuclear reactors |
US2978358A (en) * | 1958-03-28 | 1961-04-04 | Ivor E Campbell | Method of obtaining uniform coatings on graphite |
US2993814A (en) * | 1958-05-24 | 1961-07-25 | Foerderung Forschung Gmbh | Heating conductor and method of making the same |
US3092681A (en) * | 1958-09-22 | 1963-06-04 | Kanthal Ab | Electric resistance furnaces and the like |
US3121154A (en) * | 1959-10-30 | 1964-02-11 | Babcock & Wilcox Ltd | Electric heaters |
US3171871A (en) * | 1960-07-19 | 1965-03-02 | Norton Co | Method of making electrical heater bars |
US3271181A (en) * | 1963-05-29 | 1966-09-06 | Robert A Jewell | Method of coating carbonaceous base to prevent oxidation destruction and coated base |
US3337375A (en) * | 1964-04-13 | 1967-08-22 | Sprague Electric Co | Semiconductor method and device |
US3328201A (en) * | 1964-04-27 | 1967-06-27 | Rca Corp | Heater for electron tubes |
US20200113020A1 (en) * | 2018-10-05 | 2020-04-09 | Serendipity Technologies Llc | Low power high-efficiency heating element |
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