US2165310A - Filament - Google Patents
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- US2165310A US2165310A US2165310DA US2165310A US 2165310 A US2165310 A US 2165310A US 2165310D A US2165310D A US 2165310DA US 2165310 A US2165310 A US 2165310A
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- United States
- Prior art keywords
- filament
- tungsten
- iron
- wire
- temperature
- Prior art date
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 138
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 114
- 239000010937 tungsten Substances 0.000 description 112
- 229910052721 tungsten Inorganic materials 0.000 description 112
- 229910052742 iron Inorganic materials 0.000 description 60
- 238000010438 heat treatment Methods 0.000 description 56
- 238000000034 method Methods 0.000 description 48
- 239000011162 core material Substances 0.000 description 36
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 26
- 238000004804 winding Methods 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 18
- 239000002184 metal Substances 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 239000011248 coating agent Substances 0.000 description 14
- 238000000576 coating method Methods 0.000 description 14
- 229910052759 nickel Inorganic materials 0.000 description 12
- 239000007789 gas Substances 0.000 description 10
- 230000001590 oxidative Effects 0.000 description 10
- XKRFYHLGVUSROY-UHFFFAOYSA-N argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000010304 firing Methods 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- -1 rare earth metal nitrides Chemical class 0.000 description 6
- 230000003014 reinforcing Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 4
- 229910002804 graphite Inorganic materials 0.000 description 4
- 239000010439 graphite Substances 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 230000000087 stabilizing Effects 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 241000801930 Apterona helix Species 0.000 description 2
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- NMCUIPGRVMDVDB-UHFFFAOYSA-L Iron(II) chloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 2
- 235000014435 Mentha Nutrition 0.000 description 2
- 241001072983 Mentha Species 0.000 description 2
- XMVONEAAOPAGAO-UHFFFAOYSA-N Sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical class [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 238000010961 commercial manufacture process Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 229960002089 ferrous chloride Drugs 0.000 description 2
- 238000011010 flushing procedure Methods 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 150000002505 iron Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 2
- 239000011819 refractory material Substances 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/525—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length for wire, for rods
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/54—Furnaces for treating strips or wire
- C21D9/56—Continuous furnaces for strip or wire
- C21D9/62—Continuous furnaces for strip or wire with direct resistance heating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49826—Assembling or joining
- Y10T29/49881—Assembling or joining of separate helix [e.g., screw thread]
Definitions
- This invention consists in a novel process of making non-sag filaments of tungsten wire-for use in incandescent lamps.
- vllt includes within its scope the novel filament produced by the process 15 cause furnaces capable of operating at such high temperatures have a short life and are not readily available as commercial equipment.
- my invention consists in reinforcing the structure of the tungsten wire by forming a fer- 30 mils, nickel or other reinforcing alloy insurface This may be readily efportions of the wire.
- the first step consisting in subjecting the filament for aniinterval of vfrom'3 to 10 minutes to a tem- 7 perature of about 1000to;1300 C. which is a.
- the preliminary heating is carried 5 v out in an atmosphere of nitrogen, hydrogen or a non-oxidizing gas and in the presence of'iron,
- nickel or some other elementv having a lower meltingpoint and a higher vapor pressure than tungsten. Under such circumstances the iron or other metal is vaporized and deposited upon surface portions of the filament.v
- the low melting point. metal maybe present as a core upon which the tungsten wire is wound and deposited simultaneously with the preliminary step of the heat treatment, or iron maybe made available by being electrolytically deposited or plated upon the surface of the-tungsten wire by any satisfactory plating process. As a practical matter it is convenientto deposit an excess amount of 'iron or nickel upon the surface of the tungsten.
- wire, and-this may be subsequently removed by a suitable acid solvent. If an iron or nickel core has been employed, this may be dissolved at the same time and only somuch iron is left in the filamentas has entered into the molecular interstices of the tungsten structure.
- the filament is completed by subjecting it to steps which complete the settling of the tungsten crystals and cause the iron or nickel to be inter-- alloyed with the tungsten. These two changes of physical characteristics may be effected by mounting the filament in the lamp in which it is to be finally used, then raising the filament to a temperature slightly below that at which the pre-. vious heating step left off, and finally rapidly raising the temperature of the filament to approximately 2700 C.
- Fig. 1 is a sectional view, somewhat diagrammatical in form, of a furnace with a number of filament blanks in process of treatment therein.
- Fig. 2 is a diagram suggestive of the electrical heating step of the process.
- Fig. 3 is a view in perspective showing a mounted coiled filament.
- Fig. 4 is a view in elevation on a greatly enlarged scale of a portion of a triple coiled filament
- Fig. 5 is a sectional view on a still larger scale showing a filament coiled upon its mandrel and The filament .is first coiledin the shape in which it is to be eventually used in the finished lamp. If a filament of the single coil type is requlred, t sten wire ll may be coiled about an iron mandr l 40 as suggested in Fig. 5. In preparing a double or triple coiled filament the tungsten wire it may be first coiled about a tungsten mandrel 30 to form the primary coil, as shown in Fig. 4.
- the primary coil may then be coiled about aniron mandrel toform secondary coils 32 and the secondary coils, with the enclosed mandrels, may be coiled about another iron mandrel to form tertiary coils 33.
- a coil of this character is illustrated in Fig. 4.
- a number of the filament blanks ll are placedin tray 13 and inserted in a high emp rature furnace, such for example as that illustrated in Fig. 12
- This furnace is.one of a type which is commercially available and comprises an outer casing ill in which is placed a muttle H of alundum or other porous and highly refractory material.
- - A-heating coil I! for the muille is conventionally represented in Fig. l.
- the casing I0 is. providedwith an inlet pipe 14 at the upper left hand corner and with an outlet pipe I! at itslower right hand corner by means of which non-oxidizing gases, such as nitrogen or hydrogen, may be supplied to the.
- 60 double or triple coiled form are laid side by side in a tray ll of molybdenum or'of a material" which is not aii'ectedby furnace.
- the temperature of the furnace is raised to between 1000' and 1300" C. and the filament blanks subjected to this temperature for a period of about iminutes'in an atmosphere of nitrogen or hydrogen preferably which has been passed through a water bath so that ithas picked up some moisture.
- this step of the process maybe carrlcd out in a commercial furnace readily availchic and having a long life under the circum-. stances of use outlined.
- the tungsten wire is wound upon a core of iron, nickel or the like, of a lower melting point and a higher vapor pressure than the tungsten. Accordingly, at a firing temperature of 1000 to 1300 C: an appreciable amount of core material is vaporized and deposited upon the surface of the tungsten wire.
- the heat treated blanks are now removed from the furnace and allowed to cool. They are then immersed in a suitable acid, such as hydrochloric, and the iron core or cores dissolved. At the same time any excess amount of iron which may have been deposited upon the wire of the coil is also removed and the coating reduced to a thin ferrous film intimately associated with the surface structure of the tungsten.
- a suitable acid such as hydrochloric
- the filaments are given the final shape under which they are "to operate and mounted as suggested in Fig. 3.
- the coil filament is shown as supported by hooks above the end of a glass rod 2
- the filament with its mount is sealed into a lamp bulb, not shown, in'the usual manner, the bulb is exhausted and filled with argon gas, an argon-neon mixture or the like and then connected in electric circuit.
- the filament is now electrically heated to a temperature somewhat below that at which the preliminary heat treatment left off, i.
- the filament is intended for a 120 perature of approximately 1000 C.
- the voltage is raised gradually and progressively to a point at which the filament is heated to approximately 2700" C. atwhich temperature acomplete settling of the crystalline structure takes place and in a period of about one minute as suggested in.
- Fig. 5 is suggestive of the alternative step of electrolytically providing the coiled filament witha coating of iron, nickel or the like.
- the tungsten'wire 4i coiled upon a mandrel ll is immersed in a solution of ferrous chlo ride and sodium tungstate and placed in an electric circuit as the anode of a plating system.
- the iron from the solution is thus deposited in a film or coating 42 upon the core I and the coil ll.
- the thickness of the coating may be reduced to a surface film, or merely to traces of iron; in the surface structure-of the tungsten, and it is this iron which is subsequently alloyed with the tungsten by the heat treating steps on acid,"that does not maintain its shape but i8 likely 'to' alter in pitch, turns per inch,
- tungsten filament is stabilized at a temperature of 1600 to 1700" C. itis rendered brittle to an extent that causes an objectionable amount of breakage due to vibration in handling, in mounting, or in shipment.
- the preliminary heat treatment at lower temperature, followed by the final treatment at higher temperature in accordance with my novel process results in a more ductile productwell adapted to withstand the shoclns and vibrations of handling and shipping.
- non-sag tungsten filaments which is characterized by winding a tungsten wire upon an iron core to form a .helix upon the core, heating to cause iron from the core to vaporize and deposit upon the tungsten wire of n the filament, dissolving the core, andzthen heating to cause the remaining iron and tungsten to become alloyed aments, which consists in coiling tungsten wire to form a filament, heating the coiled filament to a temperature of between 1000 0. and 1300 C. to
- tungsten wire which'consists in bending tungsten wire into sub- "stantially the shape of the finished filament, heating the filament thus formed to a temperature between aboutv 1000 Grand 1300 C. in the presence of iron and in a substantially non-oxidizing atmosphere, allowing'the filament to cool, and then raising its temperature to approximately2'700" m H 5.
- the process of making tungsten filaments,- wh-ich consists in bending tungsten wire into substantially the shape of the finished filament for a volt lamp, coating the filament with iron, heating it to a temperature between 1000 C. and l300 C.,allowing it to cool, and then electrically heating it by including it in a circuit wherein the potential is raised from approximately 20 volts to approximately volts.
- non-sag ing tungsten filaments which consists in winding a tungsten wire upon a tungsten core to form a primary helix, winding the primary helix with its core upon aniron core, heating to cause iron from the iron core to vaporize and deposit upon the tungsten wire of the filament, removing the iron core, 'and then further heating to cause the deposited iron to become alloyed with the tungsten wire.
- non-sagging tungsten-filaments which consists in winding a tungsten wire upon a refractory core to form a primary helix, winding the primary helix with its core upon an iron core to form a secondary helix, winding the secondary core upon another iron core to form a tertiary helix, heating to cause iron from said cores to deposit upon the tungsten wire of the filament, removing the iron'cores, and then further heating to cause the deposited iron to become alloyed with the tungsten wireiw 11.
- the process of making non sag coiled coil tungsten filaments which consists in winding a.
Description
' Julyll, 1939. c. SPAETH 2,165,310
I f by FILAMENT Filed Aug. 14, 1936 I21 perrfior CZM d) W00 W163:
, I Patented July 11, .1939
' UNITE STATES PATENT OFFICE. r
- I I 2,165,310 I Q, I
Charles Sm fl Flushing, N. Y.. Applicatio1111Ac|::ia;ts'l4,(;:3:; 1:10. 96,040
This invention consists in a novel process of making non-sag filaments of tungsten wire-for use in incandescent lamps. vllt includes within its scope the novel filament produced by the process 15 cause furnaces capable of operating at such high temperatures have a short life and are not readily available as commercial equipment.
Other expedients relied upon in producing'nonsag tungsten .filaments have required the use of '20 additives such asthorium oxide, rare earth metal oxides or rare earth metal nitrides which are expensive to procure or require considerable skilland experience in working;
I have discovered that a satisfactory non-sag 25 filament may be produced from substantially pure tungsten wire by certain steps of procedure which obviate the difiiculties above discussed. In one aspect my invention consists in reinforcing the structure of the tungsten wire by forming a fer- 30 mils, nickel or other reinforcing alloy insurface This may be readily efportions of the wire. fected by a series of steps well adapted for processes of commercial manufacture and at little expense and may be advantageously combined 85 with a heat treatment of the filament wherein a preliminary and partial settling of the crystalline structure of the tungsten is'efiected at a temperature between 1000" and'1300 C., followed by a final heating at higher temperature after the lila- 40 menthas been mounted permanently in the lamp in which it is to serve. j
I have. found that a satisfactory crystalline ad- 1 justment of the; tungsten wire filament may be effected by aprocess havingtwo essential steps,
45 the first step consisting in subjecting the filament for aniinterval of vfrom'3 to 10 minutes to a tem- 7 perature of about 1000to;1300 C. which is a.
temperature ieasily secured in commercial furnaces. The treated filament is then cooled and" 50 'mounted in its position in an incandescent'lamp,
- surrounded by the usual argon or nitrogen gases,
heated to a temperature below the temperature 5 .used in the previous firing in the furnace .and
'then rapidly raised to a temperature, for example; 6501 approximately 2'700"v 6.. for-a 300 to 500 watt the changes above discussed.
filament. At about this temperature the final or complete settling of the crystalline structure 7 takes place whereas for filaments of smaller capacity a somewhat lower temperature will suflice.
Preferably the preliminary heating. is carried 5 v out in an atmosphere of nitrogen, hydrogen or a non-oxidizing gas and in the presence of'iron,
nickel or some other elementv having a lower meltingpoint and a higher vapor pressure than tungsten. Under such circumstances the iron or other metal is vaporized and deposited upon surface portions of the filament.v The low melting point. metal maybe present as a core upon which the tungsten wire is wound and deposited simultaneously with the preliminary step of the heat treatment, or iron maybe made available by being electrolytically deposited or plated upon the surface of the-tungsten wire by any satisfactory plating process. As a practical matter it is convenientto deposit an excess amount of 'iron or nickel upon the surface of the tungsten.
wire, and-this may be subsequently removed by a suitable acid solvent. If an iron or nickel core has been employed, this may be dissolved at the same time and only somuch iron is left in the filamentas has entered into the molecular interstices of the tungsten structure.
-The filament is completed by subjecting it to steps which complete the settling of the tungsten crystals and cause the iron or nickel to be inter-- alloyed with the tungsten. These two changes of physical characteristics may be effected by mounting the filament in the lamp in which it is to be finally used, then raising the filament to a temperature slightly below that at which the pre-. vious heating step left off, and finally rapidly raising the temperature of the filament to approximately 2700 C. This may be conveniently 1 eiiected by placing the filament in electric cirkcuit, first at' a potential of about 20 volts, and .4 thenraising the potential rapidly to approximately 120 volts, under which condition the filament is raised to incandescence and goes through The process of my invention-is applicable with special advantage to stabilizing coil filaments, for example such as the double or triple coil filaments disclosed .in my -co pending application Ser. No. 15,605, filed April 10, 1935. The fact that the new process of my invention in settling or stabilizing the structure of such coiled coil filaments requires lower temperature in the heat treat- -ment of the metal, makes the filament wire less brittle than heretofore. The-addition of the reinforcing alloy of iron or the like. reduces the I rate of evaporation of the tungsten and this in turn reduces the tendency of blackening the bulb by vaporizated deposit from the filament and therefore results in a better lumen maintenance than it has been possible to secure from lamps heretofore known.
These and other features of the invention will I be best understood and appreciated from the folcoated with an iron deposit.
lowing description of a preferred embodiment thereof and of one manner in which the process may be carried out, asillustrated in the accompanying drawing;in which- Fig. 1 is a sectional view, somewhat diagrammatical in form, of a furnace with a number of filament blanks in process of treatment therein.
Fig. 2 is a diagram suggestive of the electrical heating step of the process. I
Fig. 3 is a view in perspective showing a mounted coiled filament.
Fig. 4 is a view in elevation on a greatly enlarged scale of a portion of a triple coiled filament, and
Fig. 5 is a sectional view on a still larger scale showing a filament coiled upon its mandrel and The filament .is first coiledin the shape in which it is to be eventually used in the finished lamp. If a filament of the single coil type is requlred, t sten wire ll may be coiled about an iron mandr l 40 as suggested in Fig. 5. In preparing a double or triple coiled filament the tungsten wire it may be first coiled about a tungsten mandrel 30 to form the primary coil, as shown in Fig. 4. The primary coil may then be coiled about aniron mandrel toform secondary coils 32 and the secondary coils, with the enclosed mandrels, may be coiled about another iron mandrel to form tertiary coils 33. A coil of this character is illustrated in Fig. 4.
Having shaped the filament as above outlined, a number of the filament blanks ll are placedin tray 13 and inserted in a high emp rature furnace, such for example as that illustrated in Fig. 12 This furnace is.one of a type which is commercially available and comprises an outer casing ill in which is placed a muiile H of alundum or other porous and highly refractory material.- A-heating coil I! for the muille is conventionally represented in Fig. l. The casing I0 is. providedwith an inlet pipe 14 at the upper left hand corner and with an outlet pipe I! at itslower right hand corner by means of which non-oxidizing gases, such as nitrogen or hydrogen, may be supplied to the. furnace so that the heat treatment of the filament blanks may be carried out in a non-oxidizing atmosphere. .It will be understood that the material of the mufiie II is sufiici'ently porous to permit the gas'to permeate it. The filament blanks In in single,
60 double or triple coiled form are laid side by side in a tray ll of molybdenum or'of a material" which is not aii'ectedby furnace.
Having placed the filament blanks il in the the temperature of the furnace as above explained the temperature of the furnace is raised to between 1000' and 1300" C. and the filament blanks subjected to this temperature for a period of about iminutes'in an atmosphere of nitrogen or hydrogen preferably which has been passed through a water bath so that ithas picked up some moisture. As already explained this step of the process maybe carrlcd out in a commercial furnace readily availchic and having a long life under the circum-. stances of use outlined.
It will be noted that during this step of the treatment the tungsten wire is wound upon a core of iron, nickel or the like, of a lower melting point and a higher vapor pressure than the tungsten. Accordingly, at a firing temperature of 1000 to 1300 C: an appreciable amount of core material is vaporized and deposited upon the surface of the tungsten wire.
The heat treated blanks are now removed from the furnace and allowed to cool. They are then immersed in a suitable acid, such as hydrochloric, and the iron core or cores dissolved. At the same time any excess amount of iron which may have been deposited upon the wire of the coil is also removed and the coating reduced to a thin ferrous film intimately associated with the surface structure of the tungsten.
Having now subjected the filament blanks to a preliminary heat treatment which is effective partially to settle the crystalline structure of the tungsten, the filaments are given the final shape under which they are "to operate and mounted as suggested in Fig. 3. In this figure the coil filament is shown as supported by hooks above the end of a glass rod 2| which projects from the press 23 of the lamp. Lead wires'22 'are sealed into the press 23 and connectedto the ends of the filament. The filament with its mount is sealed into a lamp bulb, not shown, in'the usual manner, the bulb is exhausted and filled with argon gas, an argon-neon mixture or the like and then connected in electric circuit. The filament is now electrically heated to a temperature somewhat below that at which the preliminary heat treatment left off, i. e., approximately to 1000 C. If the filament is intended for a 120 perature of approximately 1000 C. the voltage is raised gradually and progressively to a point at which the filament is heated to approximately 2700" C. atwhich temperature acomplete settling of the crystalline structure takes place and in a period of about one minute as suggested in.
Fig. 2. r
Fig. 5 is suggestive of the alternative step of electrolytically providing the coiled filament witha coating of iron, nickel or the like. In this instance the tungsten'wire 4i coiled upon a mandrel ll is immersed in a solution of ferrous chlo ride and sodium tungstate and placed in an electric circuit as the anode of a plating system. The iron from the solution is thus deposited in a film or coating 42 upon the core I and the coil ll. Subsequently the thickness of the coating may be reduced to a surface film, or merely to traces of iron; in the surface structure-of the tungsten, and it is this iron which is subsequently alloyed with the tungsten by the heat treating steps on acid,"that does not maintain its shape but i8 likely 'to' alter in pitch, turns per inch,
internal diameter, etc" because the temperature .to which it has been'subjected is too low to set-f tie the crystalline structure of the wire. The
result is that under these-circumstances the coil will uncoil itself andacguire a distorted shape. 2. The process of making non-sag tungsten fll- I The process of 'my invention as above described is fully effective in settling the crystalline structure of the tungsten so that the coils will maintain their form as originally determined by the coiling machine because the vaporized ferrous coating tends-to hold the coilsin the shape originally imparted to them, and ,all this is effected without requiring a furnace treatment of over 1300 C.
- Among the numerous advantages resulting from the process of my invention is that of reducin the brittleness of the treated filament as compared with filaments of this kind heretofore known. When the crystalline structure of. a
, tungsten filament is stabilized at a temperature of 1600 to 1700" C. itis rendered brittle to an extent that causes an objectionable amount of breakage due to vibration in handling, in mounting, or in shipment. The preliminary heat treatment at lower temperature, followed by the final treatment at higher temperature in accordance with my novel process results in a more ductile productwell adapted to withstand the shoclns and vibrations of handling and shipping.
Another important advantage is in increased life of filament. This is dueto the-fact that the metal alloyed with the surface of thetungsten wire substantially reducesjhe rate of vaporization of the filament material in use. This not only reduces waste from the filament itself but reduces blackening of. the bulband thus increases .the useful life of the lamp to a marked extent as well as its burn-out life compared on a basis of equal initial efiiciency in'lumens' per watt with lamps heretofore known.
I have described the process of my invention having in 'mindparticularly the treatment of filaments for a.300 to 500 watt lamp' and while the temperatures and intervals mentioned are satisfactory for the treatment of such filaments, it will be understood that some variation in these respects is permitted and expected. For example, in treating filaments for smaller lamps a final temperature, of 2300 or 2400 C. may be adequate The time 0f treatment moreover may vary from a few seconds to several minutes depending somewhat upon the size of the filament being treated.
While it is desirable in general to carry out the heat treatment of the filament in a non-oxidizing atmosphere, it may be advantageous in some cases to include a small amount of water vapor, particularly for the purpose of removing vany graphite lubricant which may be present upon the surface of the tungsten wire. .If water vapor is present it is decomposed into hydrogen and oxygen and the oxygen will immediately combine with any traces of graphite present on the wire forming carbon monoxide or carbon dioxide whichare washed out by the hydrogen- This not only cleans the wire but prevents the formation of surface carbides which tend to make the filament brittle.
claim as new and desire to secure by Letters Patent is:
1. The process of making non-sag tungsten filaments, which is characterized by winding a tungsten wire upon an iron core to form a .helix upon the core, heating to cause iron from the core to vaporize and deposit upon the tungsten wire of n the filament, dissolving the core, andzthen heating to cause the remaining iron and tungsten to become alloyed aments, which consists in coiling tungsten wire to form a filament, heating the coiled filament to a temperature of between 1000 0. and 1300 C. to
effect a partial settling of the crystalline struc-' iron simultaneously to effect a partial settling of '15 the crystalline structure and to cause the deposition of iron vapor upon the surface of the wire, cooling the filament, and then he'atingit suinciently to effect a further settling of its crystalline structure and to cause the iron thereon to become alloyed with the tungsten.
4.. The process of making tungsten filaments,
which'consists in bending tungsten wire into sub- "stantially the shape of the finished filament, heating the filament thus formed to a temperature between aboutv 1000 Grand 1300 C. in the presence of iron and in a substantially non-oxidizing atmosphere, allowing'the filament to cool, and then raising its temperature to approximately2'700" m H 5. The process of making tungsten filaments,- wh-ich consists in bending tungsten wire into substantially the shape of the finished filament for a volt lamp, coating the filament with iron, heating it to a temperature between 1000 C. and l300 C.,allowing it to cool, and then electrically heating it by including it in a circuit wherein the potential is raised from approximately 20 volts to approximately volts.
6. The process of makingnon-sag tungsten filaments, whichconsists in winding tungsten wire to form a coil, depositing a surface film of a metal of this iron-nickel group upon the coil, heating the coated coil to a temperature'between 1000 C. and 1800 C., cooling the coilrthen again heating it to approximately 1000 C., and finally raising said temperature to above 2200 C. V n 7. The process of making non-sag tungsten filaments which consists in winding tungsten wire on a core of metal having a lower melting point.
and'a higher'vapor pressure than tungsten, firing the coil to cause the core metal to vaporize and deposit upon the tungsten wire, thencooling thestantially the shape of the finishedfllament,
coating the coil with metal of -a lower melting point and higher vapor pressurethan tungsten,
heating the coated wire to a temperature of about 1000" to 1300 C., allowing the filament to cool and then alloying said metal and tungsten by including the filament in an electric circuit wherein .the potential is sufficient to heat the filament to about 2300" to 2700 C. 9. The process of making non-sag ing tungsten filaments, which consists in winding a tungsten wire upon a tungsten core to form a primary helix, winding the primary helix with its core upon aniron core, heating to cause iron from the iron core to vaporize and deposit upon the tungsten wire of the filament, removing the iron core, 'and then further heating to cause the deposited iron to become alloyed with the tungsten wire.
10. The process of making non-sagging tungsten-filaments, which consists in winding a tungsten wire upon a refractory core to form a primary helix, winding the primary helix with its core upon an iron core to form a secondary helix, winding the secondary core upon another iron core to form a tertiary helix, heating to cause iron from said cores to deposit upon the tungsten wire of the filament, removing the iron'cores, and then further heating to cause the deposited iron to become alloyed with the tungsten wireiw 11. The process of making non sag coiled coil tungsten filaments, which consists in winding a.
tungsten wire upon an iron core to form a helix, winding said helix with its core upon a second iron core, heating to cause iron from the iron cores to vaporize and deposit upon the tungsten wire of the filament, removing both the iron cores, and then further heating to cause the remaining deposited iron to become alloyed with the tungsten' wire. 4 r
- CHARLES SPAETH.
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US2165310A true US2165310A (en) | 1939-07-11 |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2439913A (en) * | 1941-10-28 | 1948-04-20 | Gen Electric | Method of treating coiled tungsten filaments |
US2629922A (en) * | 1950-04-27 | 1953-03-03 | Gen Electric | Method of brazing resistor terminals |
US2660540A (en) * | 1949-08-18 | 1953-11-24 | Gen Electric | Metal vaporizer and method for vapor coating |
US2697772A (en) * | 1952-05-12 | 1954-12-21 | Kaiser Aluminium Chem Corp | Method of making material |
US2809140A (en) * | 1953-01-22 | 1957-10-08 | Gen Electric | Method of treating tungsten filaments |
US2881104A (en) * | 1954-12-03 | 1959-04-07 | Gen Electric Co Ltd | Methods of producing refractory metal filaments of flattened zig-zag form |
US2970961A (en) * | 1959-03-04 | 1961-02-07 | Bell Telephone Labor Inc | Magnetic material |
US3068337A (en) * | 1958-12-05 | 1962-12-11 | Gen Electric | Vaporizer and method for making the same |
US3877495A (en) * | 1972-02-04 | 1975-04-15 | Duro Test Corp | Method of manufacturing improved filaments for fluorescent lamps |
-
0
- US US2165310D patent/US2165310A/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2439913A (en) * | 1941-10-28 | 1948-04-20 | Gen Electric | Method of treating coiled tungsten filaments |
US2660540A (en) * | 1949-08-18 | 1953-11-24 | Gen Electric | Metal vaporizer and method for vapor coating |
US2629922A (en) * | 1950-04-27 | 1953-03-03 | Gen Electric | Method of brazing resistor terminals |
US2697772A (en) * | 1952-05-12 | 1954-12-21 | Kaiser Aluminium Chem Corp | Method of making material |
US2809140A (en) * | 1953-01-22 | 1957-10-08 | Gen Electric | Method of treating tungsten filaments |
US2881104A (en) * | 1954-12-03 | 1959-04-07 | Gen Electric Co Ltd | Methods of producing refractory metal filaments of flattened zig-zag form |
US3068337A (en) * | 1958-12-05 | 1962-12-11 | Gen Electric | Vaporizer and method for making the same |
US2970961A (en) * | 1959-03-04 | 1961-02-07 | Bell Telephone Labor Inc | Magnetic material |
US3877495A (en) * | 1972-02-04 | 1975-04-15 | Duro Test Corp | Method of manufacturing improved filaments for fluorescent lamps |
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