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US1832607A - Photo electric tube - Google Patents

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Publication number
US1832607A
US1832607A US109314A US10931426A US1832607A US 1832607 A US1832607 A US 1832607A US 109314 A US109314 A US 109314A US 10931426 A US10931426 A US 10931426A US 1832607 A US1832607 A US 1832607A
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Prior art keywords
potassium
container
glass
filament
ions
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Expired - Lifetime
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US109314A
Inventor
Vladimir K Zworykin
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Westinghouse Electric Corp
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Westinghouse Electric Corp
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Priority to US109314A priority Critical patent/US1832607A/en
Priority to GB13147/27A priority patent/GB271116A/en
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Publication of US1832607A publication Critical patent/US1832607A/en
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Expired - Lifetime legal-status Critical Current

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J40/00Photoelectric discharge tubes not involving the ionisation of a gas
    • H01J40/02Details
    • H01J40/04Electrodes
    • H01J40/06Photo-emissive cathodes

Definitions

  • My invention relates to photo-electric cells and it has particular relation to methods of supplying such cells with interior coatings of hoto-electrically active material.
  • time object of my invention is to provide a method of applym onidizable metal to t container.
  • Another object of my invention is to rothe above described a coating of a readily e interior surface of a coating may be applieg by electrolysis.
  • Another object of my mvention is to provide a method of coating the interior surfaces of containers with a photo-electrically active element.
  • a still further object of my invention is to provide means for practicing the-method referred to above.
  • the photo-electrically active metal is deposited on the inner wall of the cell by the electrolysis of a salt of the metal, and only exists momentarily as a the container 5 through PHOTO ELECTRIC TUBE 1926. semi R0. 108,814.
  • I contemp ate passin metallic ions directly through the walls 05 a container, and subsequentl causing the metal to be deposited on a esired portion thereof.
  • the single figure of the drawing is a view, partially in elevation, partially in cross-sectlon, and partially diagrammatic, of a preferred form of apparatus used in the practics of my invention.
  • iron crucible l is supported within a suitable heat-insulating member 2, and contains a mass 3 of molten potassium nitrate, the heat therefor being sup lied by a coil 4, or a bunsen burner (not sl iown).
  • the pressure of the clampin member 10 on the glass container 5 is a justed by the set screw 11.
  • XI, member 10 is ivotally mounted on a horizontal arm 12, a
  • umb nut 13 being used to maintain the angular adjustment thereof relative to the horizontal arm.
  • the horizontal arm 12 is provided at one end with an enlarged portion 14, having an opening 15 therethrough in order to accommgdate a vertical rod 16.
  • the portion 14 is slidable on the rod 16, and may be held in adjusted position by a set screw 17.
  • the vertical rod 16 is aflixed to a base member 18 by means of a plurality of screws 19, or by otherappropriate means.
  • the base member 18 also serves as a support for the heat insulating member 2, an the crucible 1.
  • a cooling coil 21 is attached to the horizontal arm 12, and is so arranged that it may be positioned in proximity to that portion of which passes the condoctor 7.
  • a coating 22 is shown in the drawing as being deposited on the electrode 6, and on the interior surface of the container 5 adjacent the electrode. The method of obtaining this coatin will be fully explained later.
  • the eating coil 4 is supplied with current from a source 23 while the filament 8 may 5 be supplied with heating current from a battery 24, or a transformer, gized from the source 23.
  • a m1ll1-' ammeter 27 may be included in the latter circuit, in order that the proper current flow may be maintained, and a rheostat 28 may be used to regulate the filament heating current.
  • the iron cruci-' ble is partially filled with anhydrous potassium nitrate, that is caused to fuse together into a molten mass b the application of heat.
  • the mass is prefera ly maintained at a temperature of ap roximately 335 C. during the remainder of t e process.
  • the glass container is then clamped securely to the support, and the latter is so adjusted that the container is partially submerged in the molten. potassium nitrate.
  • the vacuum pump is then started, and the container evacuated to a pressure of 10" mm. of mercury.
  • the container may be filled with an 30 inert gas, such as argon, at a suitable pressure.
  • the filament is supplied with heating current at a voltage high enough to cause incandescence, and a relatively high potential is applied between the' glowing filament and the iron crucible.
  • a relatively high potential is applied between the' glowing filament and the iron crucible.
  • the molten otassium nitrate is ionized, and it is a con uctor of electricity a portion of this potential may be considere as a plied across the glass wall of the container, etween the otassium nitrate and the filament.
  • the filament is made negative with res act to the molten mass.
  • potassium ions Under the influence of the applied potential, potassium ions travel into the interior ⁇ of the glass wall, and there displace an equivalent number of other potassium ions originally present in the glass. These ions pass to the inner surface of the container, and are immediately neutralized by electrons given off by the incandescent filament, resulting in the momentary presence of metallic potassium. At this inner surface, the temperature is far above the melting point of potassium, 625 C. and the potassium is 60 immediately vaporized, to be later deposited on cooler portions of the container. To assure its deposition on the electrode, the latter may be cooled by a coil through which water is caused to circulate, or by equiva- 65 lent means. In some cases it may not be necessary to employ special cooling means, this of course depending on the size of the container bein coated, room temperature, and other varia le factors.
  • the potassium deposits as a dense, coherent mirror, having a bi h lustre and being quite light-sensitive. I extreme sensitivity is desired, the mirror may be activated by hydrogen, as is familiar to those skilled in the art, after which the tubes may be sealed off in the customary manner.
  • the glass best suited for the container has been found by experiment to be a variety manufactured by the Corning Glass Company, under the designation G. E. 123 E. This glass contains potassium, less than 1% of lead, and is free from sodium.
  • My invention although described herein as specifically adapted to the formation of a mirror of potassium on the inner surface of an exhausted container, is not to be limited to the use of potassium alone, nor is it necessary, in all cases that the container be evacuated. In short, my invention contemplates causing any metal to be driven to the surface of a solid solution thereof, by electrolyzing such solid solution in contact with when replaced by ions from the bath no'in-.
  • Semi-skilled labor may be employed for every step in the process. with the assurance that the final product will be asg ood, if not superior to, the product of processes known and pacticed previous to my invention.
  • a photo-electric cell comprisin a glass envelope substantiall free from so um and containing not more t an one per cent of lead,
  • metallic potassium on the interior surface of a diflerent portion of said envelope an electrode within said enevolpe, and inleading wires connected to said metallic potassium and to said electrode.
  • a container capable of being evacuated and composed of glass containmg no sodium, means for evacuatin said container, a molten salt of an oxidizab e element of the alkali metal group having an atomic weight over 23.05, means vfor main-

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  • Electron Sources, Ion Sources (AREA)
  • Primary Cells (AREA)
  • Surface Treatment Of Glass (AREA)

Description

Nov. 17, 1931. v. K. ZWOR YKIN 1,332,607
PHOTO ELECTRIC TUBE Filed May 15, 1926 /5 hf //2 /3 9 W Pump lbw oono'o. 0Q van-n- I3 I. I f/ /a WITNESSES: 'NVENTOR 4 AfTORNEY la vide a method whereb Patented Nov. 17, 1931 UNITED STATES PATENT OFFICE K. ZWORYKIN, OF SWISSVALE, PENNSYLVANIA, ASSIGNOR TO WESTING- HOUSE ELECTRIC &; MANUFAOTUBING COMPANY, A CORPORATION 2mm VAN 1A Application filed Kay 15,
My invention relates to photo-electric cells and it has particular relation to methods of supplying such cells with interior coatings of hoto-electrically active material.
time object of my invention is to provide a method of applym onidizable metal to t container.
Another object of my invention is to rothe above described a coating of a readily e interior surface of a coating may be applieg by electrolysis.
Another object of my mvention is to provide a method of coating the interior surfaces of containers with a photo-electrically active element.
conditions, the alkali metals A still further object of my invention is to provide means for practicing the-method referred to above.
it has long been lmown that, under proper are extremely sensitive to light, emitting electrons proportziaonally to the amount-of light falling upon t em.
The discovery that the hydrides of the alkali metals were still more sensitive to light ing in the Physik. Zeitschrift,
is enerally ascribed to Elster and Geitel, and is fully explained in their article appear- Volume 1910. Cells containing potassium hydride as 80 the sensitive element are becoming of increas ing importance in a large variety of arts. The are used in alarm systems of various kin s; in telephotography; in systems for the grading of cigars, etc., according to color, and in eneral wherever 1t is desired to have some kind of an indication, or record, of varying light conditions.
In so far as I am aware, the majorit of the photo-electric cells now on the mar et are manufactured by a long and tedious process, involving repeated distillation of the 01385- sium in vacuum. The patent to unz, 1,381,474 discloses a typical method of manufacture that is quite costly and involves the use of a considerable amount of special ap- According to my invention, the photo-electrically active metal is deposited on the inner wall of the cell by the electrolysis of a salt of the metal, and only exists momentarily as a the container 5 through PHOTO ELECTRIC TUBE 1926. semi R0. 108,814.
the free element lprior to such deposition. In short, I contemp ate passin metallic ions directly through the walls 05 a container, and subsequentl causing the metal to be deposited on a esired portion thereof.
For a more complete understanding of my method of forming a hoto-electric cell, andof the apparatus used in the practicing of my method,attent ion is directed to the accompanylng drawing, and to the following do scription.
The single figure of the drawing is a view, partially in elevation, partially in cross-sectlon, and partially diagrammatic, of a preferred form of apparatus used in the practics of my invention.
. iron crucible l is supported within a suitable heat-insulating member 2, and contains a mass 3 of molten potassium nitrate, the heat therefor being sup lied by a coil 4, or a bunsen burner (not sl iown). A less container 5, having an electrode 6, from wiich a conductor 7 passes to the exterior, a filament 8 and an outlet 9, is held between the jaws of a clamping member 10. The pressure of the clampin member 10 on the glass container 5 is a justed by the set screw 11. The
XI, member 10 is ivotally mounted on a horizontal arm 12, a
umb nut 13 being used to maintain the angular adjustment thereof relative to the horizontal arm.
The horizontal arm 12 is provided at one end with an enlarged portion 14, having an opening 15 therethrough in order to accommgdate a vertical rod 16. The portion 14 is slidable on the rod 16, and may be held in adjusted position by a set screw 17. The vertical rod 16 is aflixed to a base member 18 by means of a plurality of screws 19, or by otherappropriate means. The base member 18 also serves as a support for the heat insulating member 2, an the crucible 1.
A cooling coil 21 is attached to the horizontal arm 12, and is so arranged that it may be positioned in proximity to that portion of which passes the condoctor 7.
A coating 22 is shown in the drawing as being deposited on the electrode 6, and on the interior surface of the container 5 adjacent the electrode. The method of obtaining this coatin will be fully explained later.
The eating coil 4 is supplied with current from a source 23 while the filament 8 may 5 be supplied with heating current from a battery 24, or a transformer, gized from the source 23.
An additional source of potential 25 1s mcluded in a circuit between the filament 8 and 10 the iron crucible, contact with the latter being made through a binding-post 26. A m1ll1-' ammeter 27 may be included in the latter circuit, in order that the proper current flow may be maintained, and a rheostat 28 may be used to regulate the filament heating current.
'(not shown) ener- In practicing my invention, the iron cruci-' ble is partially filled with anhydrous potassium nitrate, that is caused to fuse together into a molten mass b the application of heat. The mass is prefera ly maintained at a temperature of ap roximately 335 C. during the remainder of t e process. The glass container is then clamped securely to the support, and the latter is so adjusted that the container is partially submerged in the molten. potassium nitrate. The vacuum pump is then started, and the container evacuated to a pressure of 10" mm. of mercury. As an alternative, the container may be filled with an 30 inert gas, such as argon, at a suitable pressure.
Next, the filament is supplied with heating current at a voltage high enough to cause incandescence, and a relatively high potential is applied between the' glowing filament and the iron crucible. As the molten otassium nitrate is ionized, and it is a con uctor of electricity a portion of this potential may be considere as a plied across the glass wall of the container, etween the otassium nitrate and the filament. To obtain the desired results, the filament is made negative with res act to the molten mass.
lthough my invention is not to be restricted to any articular theory of operation it is my opinion that the following action takes place:
Under the influence of the applied potential, potassium ions travel into the interior} of the glass wall, and there displace an equivalent number of other potassium ions originally present in the glass. These ions pass to the inner surface of the container, and are immediately neutralized by electrons given off by the incandescent filament, resulting in the momentary presence of metallic potassium. At this inner surface, the temperature is far above the melting point of potassium, 625 C. and the potassium is 60 immediately vaporized, to be later deposited on cooler portions of the container. To assure its deposition on the electrode, the latter may be cooled by a coil through which water is caused to circulate, or by equiva- 65 lent means. In some cases it may not be necessary to employ special cooling means, this of course depending on the size of the container bein coated, room temperature, and other varia le factors.
The potassium deposits as a dense, coherent mirror, having a bi h lustre and being quite light-sensitive. I extreme sensitivity is desired, the mirror may be activated by hydrogen, as is familiar to those skilled in the art, after which the tubes may be sealed off in the customary manner.
In the Journal of the Optical Societ July, 1925, R. C. Burt has described a metli- 0d for introducing sodium into a thermionic tube by means of electrolysis. According to his report, however, he was entirely unsuccessfu in passing potassium through the tube walls in the same manner. He attributed this lack of success to the fact that sodium ions are much less mobile than potassium ions, but I have discovered that his negative results and the negative results of other investigators were caused by the differences in the dimensions and the molecular forces of sodium and otassium ions. When a glass containing ium is used, the potassium replaces thesodium ions, setting up internal strains which tend to shatter the glass.
To succemfully pass potassium through the glass wall by electrolysis, I have established the fact that it is essential that the glass be substantially free from sodium.
The glass best suited for the container has been found by experiment to be a variety manufactured by the Corning Glass Company, under the designation G. E. 123 E. This glass contains potassium, less than 1% of lead, and is free from sodium.
Although I have obtained the most consistently reliable results by employing a direct current source for the potential between the filament and the crucible, I have also been able to secure the potassium mirror when alternating potentials are used. When using alternating current, the device itself acts as a rectifier, the path between the filament and the molten potassium nitrate permitting an electron flow only from the filament. Using a current source giving a potential of 110 volts across its terminals, I have been able to pass as high as 200 milliamperes through the glass, but usually a current of 100 milliamperes will be found suitable if over-heating of the glass walls is to be avoided.
My invention, although described herein as specifically adapted to the formation of a mirror of potassium on the inner surface of an exhausted container, is not to be limited to the use of potassium alone, nor is it necessary, in all cases that the container be evacuated. In short, my invention contemplates causing any metal to be driven to the surface of a solid solution thereof, by electrolyzing such solid solution in contact with when replaced by ions from the bath no'in-.
jurious structural alterations are caused.
The principal advantage of my method of making photo-electric cells lies in its relative inexpensiveness. Methods heretofore in use have necessitated the use of elaborate apparatus, and were extremely tedious. It has always been necessary to take extreme precautions to prevent the access of the slightest trace of oxygen to the potassium,
. compelling a series of re-distillations in vacua. It has also been difficult to satisfactorily govern the amount of potassium used for each individual cell, rendering it practically impossible to produce a plurality of cells having substantially identical character- 1st1cs.
By my method, potassium in the metallic state is never exposed to air during the entire operation. Only one vacuum ump is necessary, and the whole series ofdistillations is done away with. The amount of potassium deposited in each cell may be very accurately determined by the product of the reading of the milliameter in the ionizing circuit and the time during which the container is subjected to the ionizing voltage.
Semi-skilled labor may be employed for every step in the process. with the assurance that the final product will be asg ood, if not superior to, the product of processes known and pacticed previous to my invention.
Although I have shown and described a taining the salt in a molten state and means for ionizing said salt and for causing the ions of said element to pass through a wall of the container.
3. A photo-electric cell comprisin a glass envelope substantiall free from so um and containing not more t an one per cent of lead,
potassium ions in a portion of said envelope,
metallic potassium on the interior surface of a diflerent portion of said envelope an electrode within said enevolpe, and inleading wires connected to said metallic potassium and to said electrode.
In testimony whereof, I have hereunto subscribed my name this 11th day of May,
VLADIMIR K. ZWORYKIN.
specific embodiment of the apparatus to be used in connection with the practice of my invention, other modifications will at once suggest themselves to those skilled in the art. I do not intend, therefore, to be limited except in so far as is necessitated by the prior art, or by the spirit of the following claims.
I claim as my invention:
1. In combination, a container ca able of being evacuated and composed of g ass containing no sodium, a molten salt of an oxidizable element of the alkali metal group having an atomic weight above 23.05 and means for ionizing said salt and for causing ions to pass through a wall of said container.
2. In combination, a container capable of being evacuated and composed of glass containmg no sodium, means for evacuatin said container, a molten salt of an oxidizab e element of the alkali metal group having an atomic weight over 23.05, means vfor main-
US109314A 1926-05-15 1926-05-15 Photo electric tube Expired - Lifetime US1832607A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2442617A (en) * 1942-10-31 1948-06-01 Canadian Radium & Uranium Corp Carrier for radioactive material and improved method of making the same
US2897126A (en) * 1955-03-05 1959-07-28 Quartz & Silice S A Vitreous silica and its manufacture
US2933633A (en) * 1955-02-16 1960-04-19 Gen Electric Electric discharge device
US3189395A (en) * 1961-08-29 1965-06-15 Tung Sol Electric Inc Method of making an incandescent lamp
US3773488A (en) * 1969-09-10 1973-11-20 Saint Gobain Ionic penetration of vitreous objects
US3868264A (en) * 1973-03-21 1975-02-25 Corning Glass Works Method of applying light diffusing coating to interior of incandescent lamp envelope

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2442617A (en) * 1942-10-31 1948-06-01 Canadian Radium & Uranium Corp Carrier for radioactive material and improved method of making the same
US2933633A (en) * 1955-02-16 1960-04-19 Gen Electric Electric discharge device
US2897126A (en) * 1955-03-05 1959-07-28 Quartz & Silice S A Vitreous silica and its manufacture
US3189395A (en) * 1961-08-29 1965-06-15 Tung Sol Electric Inc Method of making an incandescent lamp
US3773488A (en) * 1969-09-10 1973-11-20 Saint Gobain Ionic penetration of vitreous objects
US3868264A (en) * 1973-03-21 1975-02-25 Corning Glass Works Method of applying light diffusing coating to interior of incandescent lamp envelope

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