US3767947A - Miniaturized electric source - Google Patents
Miniaturized electric source Download PDFInfo
- Publication number
- US3767947A US3767947A US00034734A US3767947DA US3767947A US 3767947 A US3767947 A US 3767947A US 00034734 A US00034734 A US 00034734A US 3767947D A US3767947D A US 3767947DA US 3767947 A US3767947 A US 3767947A
- Authority
- US
- United States
- Prior art keywords
- source
- collector
- source according
- compound
- radiation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 230000002285 radioactive effect Effects 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 229910052722 tritium Inorganic materials 0.000 claims abstract description 9
- -1 tritium compound Chemical class 0.000 claims abstract description 5
- 239000011888 foil Substances 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 claims description 4
- 239000011324 bead Substances 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 229910052727 yttrium Inorganic materials 0.000 claims description 3
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- 239000002775 capsule Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 239000007787 solid Substances 0.000 abstract description 7
- 230000005855 radiation Effects 0.000 abstract description 5
- 239000007789 gas Substances 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012857 radioactive material Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000004308 accommodation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G04—HOROLOGY
- G04C—ELECTROMECHANICAL CLOCKS OR WATCHES
- G04C10/00—Arrangements of electric power supplies in time pieces
- G04C10/02—Arrangements of electric power supplies in time pieces the power supply being a radioactive or photovoltaic source
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21G—CONVERSION OF CHEMICAL ELEMENTS; RADIOACTIVE SOURCES
- G21G4/00—Radioactive sources
- G21G4/04—Radioactive sources other than neutron sources
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21H—OBTAINING ENERGY FROM RADIOACTIVE SOURCES; APPLICATIONS OF RADIATION FROM RADIOACTIVE SOURCES, NOT OTHERWISE PROVIDED FOR; UTILISING COSMIC RADIATION
- G21H1/00—Arrangements for obtaining electrical energy from radioactive sources, e.g. from radioactive isotopes, nuclear or atomic batteries
- G21H1/02—Cells charged directly by beta radiation
Definitions
- This invention relates to a miniaturized electric source of the type having a radioactive source emitting B-radiation, a collector for receiving this radiation and output electrodes formed by said collector and a terminal connected to said source.
- Tritium H termed T in the following specification
- T Tritium
- This invention aims to overcome the above difficulties and to provide a miniaturized source of high power output and life time, extremely low volume and simple construction. This is achieved by providing a source comprising a tritium compound in a solid state, a layer of said composition being deposited on at least one surface of a carrier, and the space between said source and said collector comprising a layer of a solid state dielectric having a thickness and density proper for allowing passage of said B-radiation at an energy in the order of up to 18 keV and for electrically insulating said source from said collector.
- T in a chemically bound solid state the problem of diffusion does no longer exist or may in any case be neglected.
- the source which is of circular shape has a metal disc 1, for instance of copper, serving as a carrier for the radioacive material.
- This material is applied to both surfaces of disc 1 in very thin layers 2.
- the thickness of such layers 2 is suitably selected in relation to the absorption of B-radiation of the available energy therein such that the radiation emitted from the innermost portion of such layers still leaves the layers in an significant amount.
- the radioactive material used is a compound of T with an element of suitable affinity.
- MT is used in the illustrated embodiment, but any other composition may be used. Similar compounds exist with Zirconium, Yttrium and other elements. The use of the one or other of the available compounds is a question of chemical stability and price.
- the illustrated embodiment LiT is applied to carrier 1 in a density of 200 mC/cm
- the coated surface of disc 1 is 2 cm so that the total amount of LiT is 400 mC in the new state of the source, and it will still be in the order of 200 mC after about 10 to 15 years.
- the radioactive source formed by carrier 1 and layers 2 is enveloped by foils 3 of plastic material flanged down and over-lapping each other along the edge of disc 1.
- Foils 3 are extremely thin in the order of 0.2;]. when their density is lg/cm, this thickness being proper on one hand for allowing passage of the B-radiation from layers 2 through foils 3 and on the other hand for electrically insulating the radioactive source from the collector.
- the collector is formed by a metallic casing 4 for instance of steel comprising two shells frictionally engaging each other along the rim. Each shell of the casing is coated at its inner surface with a layer 5 of graphite serving as an absorbtion medium avoiding reflection of electrons from the collector back towards the radioactive source.
- the casing 4, layer 5, upper plastic foil 3 and upper layer 2 of LiT have a hole for passage of a terminal wire 6 soldered to plate I.
- a metallic screen 7 is fixed on terminal wire 6 for collecting possible radiation passing through the hole of the collector. Screen 7 and the inner end of terminal 6 are imbedded in a bead 8 of plastic material, this material filling also the space between terminal 6 and the collector 4, 5, whereby all parts are properly insulated from each other.
- the B-radiation emitted by layers 2 passes through foils 3 and is collected by collector 4, 5. In this way the collector is charged to a high negative potential relatively to disc 1. Due to the extremely thin insulating foils 3 between the radioactive source and the collector the electric source hasa relatively high capacity in the order of 1,000 pF. This is advantageous particularly when the source is loaded by an oscillator as is usual in electric timepieces,where the current consumption is highly variable.
- the source is extremely compact and flat and is thus highly suitable for use in watches where it may be accommodated at one side of the timepiece, or in any other miniaturized electric or electronic instrument.
- a miniaturized electric source utilizing the energy of B-radiation emitted by radioactive tritium comprisa. a source of B-radiation comprising a metal disc having coated on at least one surface thereof a thin layer of a solid tritium compound;
- a collector element comprising a metallic casing enclosing said disc
- a dielectric layer of plastic foil enveloping said disc, interposed between said disc and said collector casing and also enclosed by said collector casing, and having a thickness and density adapted to allow passage of said B-radiation at an energy level in the order of up to 18 Rev.
- a source according to claim 1 wherein said compound is applied to said metal disc in an amount of 200 mC/cm 5.
- a source according to claim 1 wherein said collector is a metal capsule enclosing said source and plastic foil and contacting said plastic foil.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
- Power Engineering (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- X-Ray Techniques (AREA)
- Particle Accelerators (AREA)
Abstract
A miniaturized electric source having a radioactive source of Beta -radiation and a collector for said radiation, said source and said collector forming the terminals of the electric source, said source comprising a metal disc having coated thereon a tritium compound in solid state and a layer of a solid - state dielectric being disposed between said source and collector.
Description
United States Patent Adler et al.
[ MlNIATURlZED ELECTRIC SOURCE [75] Inventors: Karl Adler, Grenchen;
Georges Ducommun, Feldbrunnen, both of Switzerland [73] Assignee: Biviator S. A. Grenchen,
Switzerland [22] Filed: May 5, 1970 211 App]. No.2 34,734
[30] Foreign Application Priority Data May 7, 1969 Switzerland 7000/69 [52] US. Cl. 310/30, 310/3 A [51] Int. Cl. G0ld 7/00 [58] Field of Search 310/3 A, 3 D
[56] References Cited UNITED STATES PATENTS 2,837,666 6/1958 Linder 310/3 D 2,876,368 3/l959 Thomas 310/3 D 2,774,89l 12/1956 Dziedziula et al. 310/3 D 2,930,909 3/1960 Lieb 3l0/3 D 2,934,887 5/1960 Keller 310/3 D Primary Examiner-Benjamin A. Borchelt Assistant ExaminerN. Moskowitz Attorneylmirie & Smiley [57] ABSTRACT 9 Claims, 1 Drawing Figure 'II I PATENTEBUBIZIWH 3,767,947
7 7 A'VIIIIIA I KA R L A DL ER NVENTORG 65 8628 oucormuu 1 MIN IATURIZED ELECTRIC SOURCE This invention relates to a miniaturized electric source of the type having a radioactive source emitting B-radiation, a collector for receiving this radiation and output electrodes formed by said collector and a terminal connected to said source.
Various sources of this type have been proposed in the past, but no satisfactory results have been found for a miniaturized source adapted for use in a watch as an example, and meeting with all conditions such as safety, reliability suitablepower output and high life time in the order of to years.
Tritium (H termed T in the following specification) would be suitable as a radioactive source from a number of points of view, particularly its half-life time and the possibility of screening stray radiation, but no suitable technical solution has been known allowing use of this element in a miniaturized electric source. Due to its high ability of diffusion, vacuum used as a dielectric between the source and the collector would be destroyed within short time. Accommodation of a sufficient amount of radioactive material in a miniaturized source used to be a serious problem.
This invention aims to overcome the above difficulties and to provide a miniaturized source of high power output and life time, extremely low volume and simple construction. This is achieved by providing a source comprising a tritium compound in a solid state, a layer of said composition being deposited on at least one surface of a carrier, and the space between said source and said collector comprising a layer of a solid state dielectric having a thickness and density proper for allowing passage of said B-radiation at an energy in the order of up to 18 keV and for electrically insulating said source from said collector. When using T in a chemically bound solid state the problem of diffusion does no longer exist or may in any case be neglected. Even though T and He produced during operation will diffuse into the space between the radio-active source and the collector during operation, such gases will be contained in such a small amount between the radioactive source and the collector that passage of the B-radiation and ionisation are no problem. As far as ionisation of minute cushions of gases occurs, this is without effect because the electrical insulation between the radioactive source and the collector is obtained by said layer of solid state dielectric. For these reasons and since the space between radioactive source and collector need not be evacuated, the casing of the source must not be tightly sealed. Gases developed in the source such as He and T do not build up pressure in the casing but will easily diffuse or flow through small leaks into the ambient atmosphere. Therefore, substantially atmospheric pressure exists in the source this being particularly advantageous because chemically all available compounds of T are relatively unstable under low pressure.
This invention will now be explained in detail for one embodiment of which a cross section is illustrated on a substantially enlarged scale in the accompanying drawing.
The source which is of circular shape has a metal disc 1, for instance of copper, serving as a carrier for the radioacive material. This material is applied to both surfaces of disc 1 in very thin layers 2. The thickness of such layers 2 is suitably selected in relation to the absorption of B-radiation of the available energy therein such that the radiation emitted from the innermost portion of such layers still leaves the layers in an significant amount.
The radioactive material used is a compound of T with an element of suitable affinity. MT; is used in the illustrated embodiment, but any other composition may be used. Similar compounds exist with Zirconium, Yttrium and other elements. The use of the one or other of the available compounds is a question of chemical stability and price. ln the illustrated embodiment LiT is applied to carrier 1 in a density of 200 mC/cm The coated surface of disc 1 is 2 cm so that the total amount of LiT is 400 mC in the new state of the source, and it will still be in the order of 200 mC after about 10 to 15 years.
The radioactive source formed by carrier 1 and layers 2 is enveloped by foils 3 of plastic material flanged down and over-lapping each other along the edge of disc 1. Foils 3 are extremely thin in the order of 0.2;]. when their density is lg/cm, this thickness being proper on one hand for allowing passage of the B-radiation from layers 2 through foils 3 and on the other hand for electrically insulating the radioactive source from the collector. The collector is formed by a metallic casing 4 for instance of steel comprising two shells frictionally engaging each other along the rim. Each shell of the casing is coated at its inner surface with a layer 5 of graphite serving as an absorbtion medium avoiding reflection of electrons from the collector back towards the radioactive source.
The casing 4, layer 5, upper plastic foil 3 and upper layer 2 of LiT have a hole for passage of a terminal wire 6 soldered to plate I. A metallic screen 7 is fixed on terminal wire 6 for collecting possible radiation passing through the hole of the collector. Screen 7 and the inner end of terminal 6 are imbedded in a bead 8 of plastic material, this material filling also the space between terminal 6 and the collector 4, 5, whereby all parts are properly insulated from each other.
In operation the B-radiation emitted by layers 2 passes through foils 3 and is collected by collector 4, 5. In this way the collector is charged to a high negative potential relatively to disc 1. Due to the extremely thin insulating foils 3 between the radioactive source and the collector the electric source hasa relatively high capacity in the order of 1,000 pF. This is advantageous particularly when the source is loaded by an oscillator as is usual in electric timepieces,where the current consumption is highly variable.
Manufacture of the source is of similare simplicity as its design. After application of LiT layers 2 and of terminal wire 6 to disc 1, foils are loosely applied and then clamped between'layers 2 and layers 5 of the collector and simultaneously flanged round the edges of disc 1 by applying and closing casing shells 4. No evacuation or sealing procedure is required except for application of the insulating bead 8.
The source is extremely compact and flat and is thus highly suitable for use in watches where it may be accommodated at one side of the timepiece, or in any other miniaturized electric or electronic instrument.
What is claimed:
1. A miniaturized electric source utilizing the energy of B-radiation emitted by radioactive tritium, comprisa. a source of B-radiation comprising a metal disc having coated on at least one surface thereof a thin layer of a solid tritium compound;
b. a collector element comprising a metallic casing enclosing said disc;
c. a dielectric layer of plastic foil enveloping said disc, interposed between said disc and said collector casing and also enclosed by said collector casing, and having a thickness and density adapted to allow passage of said B-radiation at an energy level in the order of up to 18 Rev.
2. A source according to claim 1, wherein said dielectric is a plastic foil of a thickness in the order of 0.2
3. A source according to claim 1, wherein said source comprises a compound of tritium with one element of the group consisting of lithium, zirconium and yttrium.
4. A source according to claim 1, wherein said compound is applied to said metal disc in an amount of 200 mC/cm 5. A source according to claim 1, wherein said tritium compound is applied to opposite surfaces of said metal disc at a density of about 400 mC/cm 6. A source according to claim 1, wherein said source is enclosed in two plastic foils flanged down each over the rim of said metal disc.
7. A source according to claim 1 wherein said collector is a metal capsule enclosing said source and plastic foil and contacting said plastic foil.
8. A source according to claim 7 wherein said collector has a hole for passage of said terminal, the space between said terminal and collector being sealed and insulated by means of a bead of plastic material.
9. A source according to claim 1, wherein the collector surface facing said source has a coating of an absorption medium preventing reflection of electrons back toward the radioactive source.
Claims (8)
- 2. A source according to claim 1, wherein said di-electric is a plastic foil of a thickness in the order of 0.2 Mu .
- 3. A source according to claim 1, wherein said source comprises a compound of tritium with one element of the group consisting of lithium, zirconium and yttrium.
- 4. A source according to claim 1, wherein said compound is applied to said metal disc in an amount of 200 mC/cm2.
- 5. A source according to claim 1, wherein said tritium compound is applied to opposite surfaces of said metal disc at a density of about 400 mC/cm2.
- 6. A source according to claim 1, wherein said source is enclosed in two plastic foils flanged down each over the rim of said metal disc.
- 7. A source according to claim 1 wherein said collector is a metal capsule enclosing said source and plastic foil and contacting said plastic foil.
- 8. A source according to claim 7 wherein said collector has a hole for passage of said terminal, the space between said terminal and collector being sealed and insulated by means of a bead of plastic material.
- 9. A source according to claim 1, wherein the collector surface facing said source has a coating of an absorption medium preventing reflection of electrons back toward the radioactive source.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH700069A CH516231A (en) | 1969-05-07 | 1969-05-07 | Miniaturized voltage source for timing device |
Publications (1)
Publication Number | Publication Date |
---|---|
US3767947A true US3767947A (en) | 1973-10-23 |
Family
ID=4318361
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00034734A Expired - Lifetime US3767947A (en) | 1969-05-07 | 1970-05-05 | Miniaturized electric source |
Country Status (8)
Country | Link |
---|---|
US (1) | US3767947A (en) |
JP (1) | JPS4819511B1 (en) |
AT (1) | AT302439B (en) |
BR (1) | BR7018880D0 (en) |
CH (2) | CH700069A4 (en) |
FR (1) | FR2042447B1 (en) |
GB (1) | GB1235090A (en) |
NL (1) | NL7006748A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5008579A (en) * | 1989-03-03 | 1991-04-16 | E. F. Johnson Co. | Light emitting polymer electrical energy source |
US5079469A (en) * | 1990-10-15 | 1992-01-07 | The United State Of America As Represented By The United States Department Of Energy | Piezonuclear battery |
US5124610A (en) * | 1989-03-03 | 1992-06-23 | E. F. Johnson Company | Tritiated light emitting polymer electrical energy source |
US5235232A (en) * | 1989-03-03 | 1993-08-10 | E. F. Johnson Company | Adjustable-output electrical energy source using light-emitting polymer |
US5608767A (en) * | 1994-05-09 | 1997-03-04 | General Electric Company | Neutron-activated direct current source |
US5620464A (en) * | 1992-12-18 | 1997-04-15 | Angeion Corporation | System and method for delivering multiple closely spaced defibrillation pulses |
US5672928A (en) * | 1994-05-09 | 1997-09-30 | General Electric Company | Stabilized in-vessel direct current source |
US20070133733A1 (en) * | 2005-12-07 | 2007-06-14 | Liviu Popa-Simil | Method for developing nuclear fuel and its application |
US20110266916A1 (en) * | 2010-04-29 | 2011-11-03 | Donofrio Raymond S | Tritium battery |
WO2012042329A1 (en) * | 2010-09-30 | 2012-04-05 | Da Vinci Association For Inventors' Rights | Radioactive isotope electrostatic generator |
WO2022133469A1 (en) * | 2020-12-17 | 2022-06-23 | Westinghouse Electric Company Llc | Methods of manufacture for nuclear batteries |
US12198826B2 (en) | 2020-11-04 | 2025-01-14 | Westinghouse Electric Company Llc | Nuclear battery |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH539928A (en) * | 1972-05-26 | 1973-07-31 | Biviator Sa | Nuclear battery |
JPS518884B2 (en) * | 1973-03-13 | 1976-03-22 | ||
JPS5329647Y2 (en) * | 1973-09-29 | 1978-07-25 | ||
IT237213Y1 (en) * | 1995-10-12 | 2000-09-05 | Scaccabarozzi Marco | CLOCK WITH ELECTRONIC MECHANISM INCLUDED IN A SCREENING ELEMENT |
GB2363897A (en) * | 2000-06-24 | 2002-01-09 | Mathew David Platts | Radioactive decay electricity generator |
CN109994243B (en) * | 2019-04-03 | 2024-07-30 | 原子高科股份有限公司 | Radioactive source and preparation method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2774891A (en) * | 1954-11-23 | 1956-12-18 | Universal Winding Co | Means for collecting and utilizing electrical energy of nuclear transformations |
US2837666A (en) * | 1953-07-24 | 1958-06-03 | Ernest G Linder | Radioactive voltage source employing a gaseous dielectric medium |
US2876368A (en) * | 1953-04-06 | 1959-03-03 | Tracerlab Inc | Nuclear electret battery |
US2930909A (en) * | 1954-11-23 | 1960-03-29 | Leesona Corp | Radioactive battery with solid dielectric spacers and method of manufacture |
US2934887A (en) * | 1954-03-02 | 1960-05-03 | Ancienne Manufacture D Horloge | Driving device for clockwork |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1165088A (en) * | 1955-10-27 | 1958-10-17 | Radiation Res Corp | Nuclear electricity generator |
-
1969
- 1969-05-07 CH CH700069D patent/CH700069A4/xx unknown
- 1969-05-07 CH CH700069A patent/CH516231A/en not_active IP Right Cessation
-
1970
- 1970-05-05 FR FR7016332A patent/FR2042447B1/fr not_active Expired
- 1970-05-05 US US00034734A patent/US3767947A/en not_active Expired - Lifetime
- 1970-05-05 GB GB21560/70A patent/GB1235090A/en not_active Expired
- 1970-05-06 AT AT410270A patent/AT302439B/en not_active IP Right Cessation
- 1970-05-07 JP JP45038330A patent/JPS4819511B1/ja active Pending
- 1970-05-07 BR BR218880/70A patent/BR7018880D0/en unknown
- 1970-05-08 NL NL7006748A patent/NL7006748A/xx unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2876368A (en) * | 1953-04-06 | 1959-03-03 | Tracerlab Inc | Nuclear electret battery |
US2837666A (en) * | 1953-07-24 | 1958-06-03 | Ernest G Linder | Radioactive voltage source employing a gaseous dielectric medium |
US2934887A (en) * | 1954-03-02 | 1960-05-03 | Ancienne Manufacture D Horloge | Driving device for clockwork |
US2774891A (en) * | 1954-11-23 | 1956-12-18 | Universal Winding Co | Means for collecting and utilizing electrical energy of nuclear transformations |
US2930909A (en) * | 1954-11-23 | 1960-03-29 | Leesona Corp | Radioactive battery with solid dielectric spacers and method of manufacture |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5124610A (en) * | 1989-03-03 | 1992-06-23 | E. F. Johnson Company | Tritiated light emitting polymer electrical energy source |
US5235232A (en) * | 1989-03-03 | 1993-08-10 | E. F. Johnson Company | Adjustable-output electrical energy source using light-emitting polymer |
US5008579A (en) * | 1989-03-03 | 1991-04-16 | E. F. Johnson Co. | Light emitting polymer electrical energy source |
US5079469A (en) * | 1990-10-15 | 1992-01-07 | The United State Of America As Represented By The United States Department Of Energy | Piezonuclear battery |
US5620464A (en) * | 1992-12-18 | 1997-04-15 | Angeion Corporation | System and method for delivering multiple closely spaced defibrillation pulses |
US5672928A (en) * | 1994-05-09 | 1997-09-30 | General Electric Company | Stabilized in-vessel direct current source |
US5608767A (en) * | 1994-05-09 | 1997-03-04 | General Electric Company | Neutron-activated direct current source |
US20070133733A1 (en) * | 2005-12-07 | 2007-06-14 | Liviu Popa-Simil | Method for developing nuclear fuel and its application |
US20110266916A1 (en) * | 2010-04-29 | 2011-11-03 | Donofrio Raymond S | Tritium battery |
WO2012042329A1 (en) * | 2010-09-30 | 2012-04-05 | Da Vinci Association For Inventors' Rights | Radioactive isotope electrostatic generator |
US12198826B2 (en) | 2020-11-04 | 2025-01-14 | Westinghouse Electric Company Llc | Nuclear battery |
WO2022133469A1 (en) * | 2020-12-17 | 2022-06-23 | Westinghouse Electric Company Llc | Methods of manufacture for nuclear batteries |
US12080435B2 (en) | 2020-12-17 | 2024-09-03 | Westinghouse Electric Company Llc | Methods of manufacture for nuclear batteries |
Also Published As
Publication number | Publication date |
---|---|
AT302439B (en) | 1972-10-10 |
FR2042447A1 (en) | 1971-02-12 |
CH700069A4 (en) | 1971-07-15 |
CH516231A (en) | 1971-11-30 |
BR7018880D0 (en) | 1973-03-15 |
FR2042447B1 (en) | 1973-10-19 |
NL7006748A (en) | 1970-11-10 |
JPS4819511B1 (en) | 1973-06-14 |
GB1235090A (en) | 1971-06-09 |
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