US1965585A - Electric gaseous discharge device - Google Patents
Electric gaseous discharge device Download PDFInfo
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- US1965585A US1965585A US397798A US39779829A US1965585A US 1965585 A US1965585 A US 1965585A US 397798 A US397798 A US 397798A US 39779829 A US39779829 A US 39779829A US 1965585 A US1965585 A US 1965585A
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- electrodes
- envelope
- discharge device
- gaseous discharge
- oxide
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- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- 238000007789 sealing Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 8
- 229910052749 magnesium Inorganic materials 0.000 description 8
- 239000011777 magnesium Substances 0.000 description 8
- 235000001055 magnesium Nutrition 0.000 description 8
- 229940091250 magnesium supplement Drugs 0.000 description 8
- 229910052786 argon Inorganic materials 0.000 description 6
- 238000011049 filling Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229910052754 neon Inorganic materials 0.000 description 5
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 5
- 238000004544 sputter deposition Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000001994 activation Methods 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 230000002238 attenuated effect Effects 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000011233 carbonaceous binding agent Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 230000005686 electrostatic field Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 150000002927 oxygen compounds Chemical class 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J17/00—Gas-filled discharge tubes with solid cathode
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2893/00—Discharge tubes and lamps
- H01J2893/0064—Tubes with cold main electrodes (including cold cathodes)
Definitions
- the particular object of the invention is to provide a gaseous discharge device which will start with a cold cathode upon the application of a relatively low potential, will operate at a correspondingly low potential, and will maintain these characteristics throughout a long useful life.
- Another object of the invention is to provide a gaseous discharge device which will be extremely simple and inexpensive in construction.
- a further object of the invention is to provide a method of producing such a discharge. device.
- Fig. 1 is an elevation of the glass tubing used to 50 form the envelope
- the cylindrical electrodes 3 which are preferably 7 of nickel or the like, are each welded at one end to the ends of an inlead 4 of dumet or other material having a suitable coeflicient of expansion for sealing into the tube 1.
- a vitreous bead 5 which is fused to the inleads 4 near the electrodes 3 3 maintains said electrodes with their axes parallel, and with a space of about a millimeter between said electrodes.
- One of said electrodes has welded thereto adjacent to the inlead end a small piece 6 of magnesium, calcium or the like, magnesium being preferred because of. greater ease inhandling during manufacture of the device. In practice the electrode 3 is slightly flattened at this point to facilitate the welding operation.
- Each of the electrodes 3 is then coated with an alkaline or alkaline earth oxygen compound.
- This compound can be the oxide, but since it is difficult to maintain the purity of the oxide in the air it is preferably one which will readily decompose under the influence of ionic bombardment, such as the carbonate or nitrate of barium or of strontium. A mixture of the carbonates of barium and strontium, for example, gives very good results.
- the device is connected by the inleads 4 to a source of electrical energy of high potential, high frequency and steep wave front, a discharge thereupon occurring between said electrodes 3.
- a source of electrical energy of high potential, high frequency and steep wave front a discharge thereupon occurring between said electrodes 3.
- an electrostatic field of high intensity is set up adjacent to said electrodes which causes a severe bombardment of said electrodes by the positiveions generated by said discharge.
- This bombardment results in the decomposition of both the alkaline compound and the carbonaceous binder, and in the sputtering of the mag nesium 6.
- the magnesium being thus in a finely divided state readily combines with the free oxygen atoms given up by the alkaline compound and reduces the carbon dioxide which is also evolved.
- the method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with an alkaline compound which is reducible to the oxide, attaching a small quantity of a metal having a high afiinity for oxygen to one of said electrodes, sealing said electrodes into an envelope, evacuating said envelope while heating it to drive off substantially all occluded gases and vapors, filling said envelope with an attenuated atmosphere of rare gas, sealing off said envelope, and creating a high potential, high frequency discharge. of steep wave front between said electrodes to reduce substantially all of said alkaline compound to the oxide.
- the method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with barium carbonate, attaching a piece of magnesium to one of said electrodes, sealing said electrodes into an envelope, evacuating said envelope while heating it to drive off substantially all occluded gases and vapors, filling said envelope with neon containing a small percentage of argon at a pressure of 40-50 m. m. of mercury, sealing off said envelope, and creating a high potential, high frequency discharge of steep wave front between said electrodes to reduce substantially all said barium carbonate to the oxide and to reduce some of said oxide to the metallic form.
- the method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with an alkaline compound reducible to the oxide, attaching a small quantity of a metal having a high afiinity for oxygen to one of said electrodes, sealing said electrodes in an envelope, evacuating said envelope while heating it to drive off substantially all occluded gases and vapors, filling said envelope with an attenuated atmosphere of rare gas containing a small percentage of a common gas, sealing said envelope, and creating a high potential, high frequency discharge of steep wave front between said electrodes to reduce substantially all of said compound to the oxide, with a small amount thereof further reduced to the metallic form.
- An electric gaseous discharge device comprising a tubular envelope of small diameter, electrodes sealed thereinto, at least one of said electrodes having a coating ofbarium oxide and barium thereon, and a gaseous atmosphere in said envelope consisting of a mixture of neon with .'I% argon at a pressure of 40-50 m. m. of mercury.
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- Vessels And Coating Films For Discharge Lamps (AREA)
Description
.Fufly 10-, 193 T. E. FOULKE ELECTRIC GASEOUS DISCHARGE DEVICE Filed Oct. 7, 1929 HIS ATTORNEY Patented July 10, 1934 1,965,585 ELECTRIC GASEOUS DISCHARGE DEVICE Ted E. Foulke, Nutley, N. 1., assignor to General Electric Vapor Lamp Company, Hoboken, N. 1., a corporation of New Jersey Application October I, 1929, Serial No. 397,798
6 Claims.
The present invention relates to electric discharge devices, and to electrodes therefor.
The particular object of the invention is to provide a gaseous discharge device which will start with a cold cathode upon the application of a relatively low potential, will operate at a correspondingly low potential, and will maintain these characteristics throughout a long useful life. Another object of the invention is to provide a gaseous discharge device which will be extremely simple and inexpensive in construction. A further object of the invention is to provide a method of producing such a discharge. device. Other objects and advantages of the invention will appear from the following detailed description of a gaseous discharge device embodying my invention or from an inspection of the accompanying draw- The invention consists of certain new and novel features of construction and combinations of parts and also in the new and novel steps in the process of manufacture thereof, as hereinafter set forth and claimed.
Despite the many advantages of electric gaseous discharge devices of the cathode glow tube for such uses as signals, indicators, signs and other purposes where a low intensity light source will suffice these devices have not been extensively used, largely due to the fact that it has been, impossible to produce such a device which would function on normal commercial potentials. The production of such a device which would operate on 110 volts D. C., and at the same time have a reasonablylong useful life, has been an especially difilcult problem. I have discovered a new process of activating the cathode which results in an electrode having not only an extremely low work function but also a low sputtering rate. This new process is especially effective in the manufacture of lamps having very small electrodes thus making possible for the first time the production of such devices of exceedingly small sizes, to wit: complete lamps having bulbs of about one eighth and about one quarter of an inch in diameter. Discharge devices constructed according to this invention will start upon the application of low potentials either alternating or direct current and as low as 50 volts D. C. and have a useful life of several hundred to several thousand hours, depending upon the current density employed. I have further found that the cost of a device of this type may be materially reduced by fabricating the envelope from glass tubing instead of the conventional blown bulb.
For the purpose of illustration I have shown a gaseous discharge device embodying my invention, as it appears at several stages in the manufacture thereof, in the accompanying drawing,.in which Fig. 1 is an elevation of the glass tubing used to 50 form the envelope,
Fig. 2 is an elevation of the electrode assembly,
Fig. 3 is an elevation of the device before sealing oil, and
Fig. 4 is an elevation of the completed device, 5 which is especially designed for use, in combination with a suitable series resistance, in testing electrical circuits of varying voltages to determine whether they are energized, but which is also useful for many other purposes.
In the drawing a piece of tubing 1 of glass or other vitreous material of say A, inch diameter and of about one inch or other suitable length is utilized for the gas tight envelope of the device.
The cylindrical electrodes 3 which are preferably 7 of nickel or the like, are each welded at one end to the ends of an inlead 4 of dumet or other material having a suitable coeflicient of expansion for sealing into the tube 1. A vitreous bead 5 which is fused to the inleads 4 near the electrodes 3 3 maintains said electrodes with their axes parallel, and with a space of about a millimeter between said electrodes. One of said electrodes has welded thereto adjacent to the inlead end a small piece 6 of magnesium, calcium or the like, magnesium being preferred because of. greater ease inhandling during manufacture of the device. In practice the electrode 3 is slightly flattened at this point to facilitate the welding operation. Each of the electrodes 3 is then coated with an alkaline or alkaline earth oxygen compound. This compound can be the oxide, but since it is difficult to maintain the purity of the oxide in the air it is preferably one which will readily decompose under the influence of ionic bombardment, such as the carbonate or nitrate of barium or of strontium. A mixture of the carbonates of barium and strontium, for example, gives very good results. This compound is v most conveniently applied by mixing it with a vehicle, preferably one which will decompose when heated in a vacuum leaving a carbonaceous residue, collodion, or a solution of cellulose in ethyl acetate, for example, and sprayed or painted on the electrodes, or the electrodes are dipped there- After the electrodes are dry the complete electrode assembly, as shown in Fig. 2, is inserted within the tube 1 and the end of said tube 1 insert to form a pinch seal on the inleads 4, as no temperature of from 400 C. to 450 C. for several minutes in order to drive out substantially all water vapor, occluded gases and vaporizable material. While still connected to the exhaust system the tube 1 is allowed to cool to atmospheric temperature, after which it is filled with A filling of neon a suitable gaseous atmosphere. with about 31% of argon at a pressure of 40-50 mm. of mercury has been found to give the lowest breakdown potential which is consistent with long life of thedevice. Satisfactory results may also be obtained with mixtures of neon with from .1% to about 3% of argon, but with the higher percentages of argon the luminosity of the device a is somewhat impaired. The pressure may likewise be varied, but either an increase or a decrease from the range given above results in increased breakdown potential. It has been found that small traces of impurities such as oxygen, nitrogen, carbon dioxide, hydrogen, air, and the like-water vapor and hydrocarbons being excepted-improve the lamp in certain respects which will be set forth hereinafter, al-
though their use is not recommended if extremely low breakdown potential is desired.
After receiving its gaseous filling the tube 1 is then sealed off at the constriction 7. as shown in Fig. 4, the device being complete except forthe activation of the electrodes.
To activate the electrodes 3 the device is connected by the inleads 4 to a source of electrical energy of high potential, high frequency and steep wave front, a discharge thereupon occurring between said electrodes 3. Due to the shape of the electrodes 3 and to the wave shape impressed thereon an electrostatic field of high intensity is set up adjacent to said electrodes which causes a severe bombardment of said electrodes by the positiveions generated by said discharge. This bombardment results in the decomposition of both the alkaline compound and the carbonaceous binder, and in the sputtering of the mag nesium 6. The magnesium being thus in a finely divided state readily combines with the free oxygen atoms given up by the alkaline compound and reduces the carbon dioxide which is also evolved. This bombardment is continued until substantially all the alkaline compound has been reduced to the oxide, with a small portion thereof still further reduced, probably all of it to the metallic form. This intermixture of oxide and metal has an extremely low work function, which results in the device having a correspondingly low breakdown potential. The function of the carbon residue from the carbonaceous vehicle inthis activation process is not entirely understood, but
device is then ready for any suitable commercial application.
The operating characteristics of such a device will remain substantially uniform throughout its useful life, despite the slight sputtering of the alkaline metal from the electrodes during operation, due to the fact that more metal'is reduced by the same ionic bombardment which causes the sputtering.
During the activation process a certain amount of blackening appears .on the wall of the envelope 1, due to the sputtering of the magnesium 6 and of the electrode material. By placing the magnesium 6 at the lower end of the electrode 3 this blackening is'substantially confined to the inlcad end of the envelope 1 and does not seriously impair the light emission from the device. It has been found-,- however, that traces of the order of 0.1-1.0 of oxygen, nitrogen, or other impurities, as set forth above, tend to reduce this blackening and hence are desirable in certain cases. One theory of the eflect of these gases is that they aid in cementing the activating material into a monomolecular layer on the electrodes, although this is uncertain. The blackening is, however, markedly decreased in certain cases.
While I have illustrated and described my invention in connection with a-particular gaseous discharge device it is to be understood that various changes, substitutions and omissions. within the scope of the appended claims, may be made in the structure and in the steps of the process without departing from the spirit of my invention. The-term alkaline", as used in these claims, is intended to refer to either the true alkali metals, or to the metals of the alkaline earth group.
I claim:
1. The method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with an alkaline compound which is reducible to the oxide, attaching a small quantity of a metal having a high afiinity for oxygen to one of said electrodes, sealing said electrodes into an envelope, evacuating said envelope while heating it to drive off substantially all occluded gases and vapors, filling said envelope with an attenuated atmosphere of rare gas, sealing off said envelope, and creating a high potential, high frequency discharge. of steep wave front between said electrodes to reduce substantially all of said alkaline compound to the oxide.
2. The method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with barium carbonate, attaching a piece of magnesium to one of said electrodes, sealing said electrodes into an envelope, evacuating said envelope while heating it to drive off substantially all occluded gases and vapors, filling said envelope with neon containing a small percentage of argon at a pressure of 40-50 m. m. of mercury, sealing off said envelope, and creating a high potential, high frequency discharge of steep wave front between said electrodes to reduce substantially all said barium carbonate to the oxide and to reduce some of said oxide to the metallic form.
3. The method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with barium carbonate, strontium carbonate, and a carbonaceous substance, attaching a piece of magnesium to one of said electrodes, sealing said electrodes into an envelope, evacuating said envelope while heating it to drive ofi substantially all occluded gases and vapors, filling said envelope with neon containing about 37% of argon at a pressure of 40-50 m. m. of mercury, sealing oil said envelope, and creating a high potential, high frequency discharge of steep wave front between said electrodes to reduce substantially all of said carbonates to the oxide and to reduce some of said oxide tube, and creating a. high potential, high frequency discharge of steep wave front between said electrodes to reduce substantially all of said alkaline compound to the oxide form, with a small quantity thereof further reduced to the metallic form.
5. The method of producing an electric gaseous discharge device which comprises coating the electrodes thereof with an alkaline compound reducible to the oxide, attaching a small quantity of a metal having a high afiinity for oxygen to one of said electrodes, sealing said electrodes in an envelope, evacuating said envelope while heating it to drive off substantially all occluded gases and vapors, filling said envelope with an attenuated atmosphere of rare gas containing a small percentage of a common gas, sealing said envelope, and creating a high potential, high frequency discharge of steep wave front between said electrodes to reduce substantially all of said compound to the oxide, with a small amount thereof further reduced to the metallic form.
6. An electric gaseous discharge device comprising a tubular envelope of small diameter, electrodes sealed thereinto, at least one of said electrodes having a coating ofbarium oxide and barium thereon, and a gaseous atmosphere in said envelope consisting of a mixture of neon with .'I% argon at a pressure of 40-50 m. m. of mercury.
TED E. FOULKE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US397798A US1965585A (en) | 1929-10-07 | 1929-10-07 | Electric gaseous discharge device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US397798A US1965585A (en) | 1929-10-07 | 1929-10-07 | Electric gaseous discharge device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1965585A true US1965585A (en) | 1934-07-10 |
Family
ID=23572660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US397798A Expired - Lifetime US1965585A (en) | 1929-10-07 | 1929-10-07 | Electric gaseous discharge device |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1965585A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419902A (en) * | 1944-03-10 | 1947-04-29 | Sylvania Electric Prod | Fluorescent electric discharge lamp |
| US2537225A (en) * | 1947-04-22 | 1951-01-09 | Continental Electric Company | Photoelectric tube and method of manufacture |
| US2560933A (en) * | 1949-02-17 | 1951-07-17 | Sylvania Electric Prod | Lamp electrode |
| US2607901A (en) * | 1946-12-31 | 1952-08-19 | Bell Telephone Labor Inc | Electronic discharge device |
| US2671184A (en) * | 1949-12-01 | 1954-03-02 | Gen Electric | Flashing discharge device |
| US2844433A (en) * | 1952-11-21 | 1958-07-22 | Rauland Corp | Method of manufacture for electric discharge devices |
| US2874324A (en) * | 1952-07-23 | 1959-02-17 | Int Standard Electric Corp | Electric gaseous discharge tubes |
| US3335311A (en) * | 1965-02-01 | 1967-08-08 | Gen Electric | Glow discharge device having parallel permanent magnetic rod electrodes |
| US3806761A (en) * | 1971-08-23 | 1974-04-23 | Owens Illinois Inc | Gas discharge device with improved memory margin |
| US5017831A (en) * | 1987-12-30 | 1991-05-21 | Gte Products Corporation | Glow discharge lamp with getter material on anode |
-
1929
- 1929-10-07 US US397798A patent/US1965585A/en not_active Expired - Lifetime
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419902A (en) * | 1944-03-10 | 1947-04-29 | Sylvania Electric Prod | Fluorescent electric discharge lamp |
| US2607901A (en) * | 1946-12-31 | 1952-08-19 | Bell Telephone Labor Inc | Electronic discharge device |
| US2537225A (en) * | 1947-04-22 | 1951-01-09 | Continental Electric Company | Photoelectric tube and method of manufacture |
| US2560933A (en) * | 1949-02-17 | 1951-07-17 | Sylvania Electric Prod | Lamp electrode |
| US2671184A (en) * | 1949-12-01 | 1954-03-02 | Gen Electric | Flashing discharge device |
| US2874324A (en) * | 1952-07-23 | 1959-02-17 | Int Standard Electric Corp | Electric gaseous discharge tubes |
| US2844433A (en) * | 1952-11-21 | 1958-07-22 | Rauland Corp | Method of manufacture for electric discharge devices |
| US3335311A (en) * | 1965-02-01 | 1967-08-08 | Gen Electric | Glow discharge device having parallel permanent magnetic rod electrodes |
| US3806761A (en) * | 1971-08-23 | 1974-04-23 | Owens Illinois Inc | Gas discharge device with improved memory margin |
| US5017831A (en) * | 1987-12-30 | 1991-05-21 | Gte Products Corporation | Glow discharge lamp with getter material on anode |
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