EP0362947A1 - Mit einer multizellulären Ionenquelle mit magnetischem Einschluss versehene abgeschmolzene Neutronenröhre - Google Patents
Mit einer multizellulären Ionenquelle mit magnetischem Einschluss versehene abgeschmolzene Neutronenröhre Download PDFInfo
- Publication number
- EP0362947A1 EP0362947A1 EP89202465A EP89202465A EP0362947A1 EP 0362947 A1 EP0362947 A1 EP 0362947A1 EP 89202465 A EP89202465 A EP 89202465A EP 89202465 A EP89202465 A EP 89202465A EP 0362947 A1 EP0362947 A1 EP 0362947A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- holes
- ion source
- anode
- neutron tube
- ion
- 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.)
- Granted
Links
- 238000010884 ion-beam technique Methods 0.000 claims abstract description 10
- 229910052722 tritium Inorganic materials 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims abstract description 8
- 230000004927 fusion Effects 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 4
- 150000002500 ions Chemical class 0.000 claims description 49
- 238000001816 cooling Methods 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims description 2
- 230000003628 erosive effect Effects 0.000 description 10
- 239000007789 gas Substances 0.000 description 7
- 230000007423 decrease Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052805 deuterium Inorganic materials 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000010849 ion bombardment Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- 229910052691 Erbium Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- -1 deuterium ions Chemical class 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 238000001956 neutron scattering Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05H—PLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
- H05H3/00—Production or acceleration of neutral particle beams, e.g. molecular or atomic beams
- H05H3/06—Generating neutron beams
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J27/00—Ion beam tubes
- H01J27/02—Ion sources; Ion guns
- H01J27/04—Ion sources; Ion guns using reflex discharge, e.g. Penning ion sources
Definitions
- the invention relates to a sealed neutron tube containing a low-pressure deuterium-tritium gas mixture from which an ion source with two electrodes (anode and cathode) forms an ionized gas channeled by a confining magnetic field created by magnets or by any other means of creating said field, said source emitting from emission channels made in said cathode ion beams which pass through an extraction-acceleration electrode and are projected at high energy onto a target electrode to produce there a fusion reaction resulting in the emission of neutrons.
- Neutron tubes of the same kind are used in the techniques of examination of matter by fast, thermal, epithermal or cold neutrons: neutronography, analysis by activation, analysis by spectrometry of inelastic diffusions or radiative captures, neutron scattering etc. .
- the d (3 H , 4 He ) n fusion reaction delivering 14 MeV neutrons is usually the most used due to its large cross section for relatively low ion energies.
- the number of neutrons obtained per unit of charge passing through the beam is always increasing as the energy of the ions directed towards a thick target is itself increasing and this largely at the beyond the energies of the ions obtained in the sealed tubes currently available and supplied by a THT not exceeding 250 kV.
- the erosion of the target by ion bombardment is one of the most determining.
- Erosion is a function of the chemical nature and structure of the target on the one hand, the energy of the incident ions and their density distribution profile on the impact surface on the other.
- the target consists of a hydrurable material (Titanium, Scandium, Zirconium, Erbium etc ...) capable of fixing and releasing large quantities of hydrogen without significant disturbance of its mechanical strength; the total quantity set is a function of the target temperature and the hydrogen pressure in the tube.
- the target materials used are deposited in the form of thin layers, the thickness of which is limited by problems of adhesion of the layer to its support.
- One way to delay erosion of the target is, for example, to form the absorbent active layer from a stack of identical layers isolated from each other by a diffusion barrier. The thickness of each of the active layers is of the order of the depth of penetration of the deuterium ions coming to strike the target.
- Another way of protecting the target and therefore of increasing the lifetime of the tube consists in acting on the ion beam so as to improve its density distribution profile on the impact surface. At a constant total ion current on the target, which results in a constant neutron emission, this improvement will result from a distribution as uniform as possible of the current density over the entire surface offered by the target to the bombardment of the ions.
- the ions are generally supplied by a Penning type ion source which has the advantage of being robust, of being cold cathode (hence a long service life), of give large discharge currents for low pressures (of the order of 10 A / torr), to have a high extraction yield (from 20 to 40%) and to be of small dimensions.
- This type of source has the drawback of requiring a magnetic field of the order of a thousand gauss, parallel to the axis of the ionization chamber, introducing significant transverse inhomogeneity in current density of the ions at the inside the landfill and at the level of the extraction which takes place along the common axis of the field and the source.
- the object of the invention is to provide a source device enabling these disadvantages to be overcome.
- said ion source is of multicellular type consisting of a structure of elementary cells of Penning type comprising for all of said cells a cavity cathode inside of which is disposed a multi-hole anode, the axes of said holes being aligned respectively on the corresponding axes of said emission channels, the number of said holes being optimized so as to increase the extracted ion beam for equivalent bulk of said ion source, the shape and / or dimensions and / or positioning of said holes being adapted to the topology of said magnetic field.
- an additional gain in the discharge current may result from the increase in length of the structure of the multicellular ion source. This gain can go up to a factor of 2.
- the increase in current resulting from the new source configuration can then be used to reduce the operating pressure of the neutron tube and thus limit the harmful impact of ion-gas reactions.
- the feasibility of the multicell structure assumes that a magnetic field is suitable for the proper functioning of a Penning structure, in particular at the level of the relationship between the magnetic induction and the hole radius of the multi-hole anode.
- the variation of the magnetic field in level and according to the shape of the lines of force can be corrected by an increase in said radius, which amounts to making structures with a variable anode radius.
- a better adaptation of the shape of the anode to the magnetic lines of force can be obtained by replacing the cylindrical structures of circular or square section by frustoconical structures so as to make the generators of truncated cones coincide with the lines of force that build on the contours of the holes.
- the ions of the different structures are emitted through channels made in the cathode acting as an emission electrode. These channels, the number of which is identical to that of the elementary cells, are arranged respectively along the same axes of symmetry. In the case of structures with a circular section, the diameter is a function of the electric field applied and the thickness of the electrode.
- a variant of this system consists in introducing an expansion chamber below the cathodes in order to standardize the densities in the vicinity of the emission which then takes place through orifices the arrangement of which can be almost independent of that of the elementary cells.
- the extraction-acceleration electrode can be constituted by an electrode provided with n orifices having axes corresponding respectively to those of the n elementary cells, or with j orifices smaller than the number of n elementary cells and therefore diameters greater than those of the emission channels and whose arrangement avoids any interception of the beams.
- This extraction-acceleration electrode can be increased in order to improve the mechanical strength and to allow cooling by forced circulation of fluid.
- FIG. 1 shows the main basic elements of a sealed neutron tube 11 containing a gaseous mixture under low pressure to be ionized such as deuterium-tritium and which comprises an ion source 1 and an extraction-acceleration electrode 2 between which there is a very high potential difference allowing the extraction and acceleration of the ion beam 3 and its projection on the target 4 where the fusion reaction takes place resulting in the emission of neutrons at 14 MeV for example.
- a sealed neutron tube 11 containing a gaseous mixture under low pressure to be ionized such as deuterium-tritium and which comprises an ion source 1 and an extraction-acceleration electrode 2 between which there is a very high potential difference allowing the extraction and acceleration of the ion beam 3 and its projection on the target 4 where the fusion reaction takes place resulting in the emission of neutrons at 14 MeV for example.
- the ion source 1 secured to an insulator 5 for the passage of the THT supply connector is a Penning type source for example, consisting of a cylindrical anode 6, a cathode cavity 7 to which is incorporated a magnet 8 with an axial magnetic field which confines the ionized gas 9 around the axis of the anode cylinder and whose lines of force 10 show a certain divergence.
- An ion emission channel 12 is formed in said cathode cavity opposite the anode.
- FIG. 2a shows the profile of the density J of bombardment of the ions in any radial direction Or, from the point of impact 0 of the central axis of the beam on the target surface.
- the shape of this profile highlights the inhomogeneous nature of this beam whose very high density in the central part decreases rapidly when one moves away from it.
- erosion takes place as a function of the bombardment density and the entire layer of hydrurable material of thickness e deposited on a substrate S is saturated with a deuterium-tritium mixture.
- the depth of penetration of the deuterium-tritium energy ions represented in dotted lines is effected over a depth which is a function of this energy.
- the erosion of the layer is such that the penetration depth l2 is greater than the thickness e in the most bombarded part; a part of the incident ions is implanted in the substrate and very quickly the atoms of deuterium and tritium are in supersaturation.
- FIG. 3 shows a neutron tube provided with a Pennell type multicellular ion source consisting of a cathode cavity 7 and a multi-hole anode 6, brought to a potential 4 to 8 kV higher than that of the cathode cavity itself brought to a very high voltage of 250 kV for example.
- a Pennell type multicellular ion source consisting of a cathode cavity 7 and a multi-hole anode 6, brought to a potential 4 to 8 kV higher than that of the cathode cavity itself brought to a very high voltage of 250 kV for example.
- the magnet 8 provides a magnetic field for confining the ionized gas of the order of a thousand gauss.
- the invention consists in exploiting the property of multicellular discharge structures with containment of magnetic type, namely that for the same anode section, the discharge current as well as the current of the ion beam extracted from this discharge are respectively greater in the case of a multicellular source structure than the same currents obtained in the case of a single-cell structure. Likewise, it is more advantageous to use a multicell structure with n anode holes than a multicell structure with m holes if n> m.
- Each section of the structure with n holes is then smaller than each of the sections of the structure with m holes; but the aforementioned advantage is only ensured if the anode section remains equivalent for said structures, which makes it possible to reduce the pressure of the gaseous mixture and therefore the probability of ion-gas reactions.
- the number of orifices made in the extraction-acceleration electrode is less than that of the beams coming from the source: for example each orifice 13 of this electrode 2 delivers passage to two beams from the source as shown in the figure.
- the divergence of the lines of force of the magnetic field shows that it is very high in the central zone and gradually decreases to a very low value on the periphery.
- the anode holes 6′1, 6′2, ..., 6 ′ n are formed as shown in FIG. 5 with radii varying in opposite directions to the magnetic field so that the product of magnetic induction by the anode radius remains substantially constant. This arrangement tends to standardize the ion current density.
- the device shown in Figure 6 provides a significant improvement in that the anode holes 6 ⁇ 1, 6 ⁇ 2, ..., 6 ⁇ n have frustoconical shapes which approximate the lines of force of the magnetic field.
- an expansion chamber 14 is arranged below the cathodes in order to standardize the ion densities.
- the emission is carried out through orifices 15 the number of which can be independent of that of the holes of the multi-hole anode.
- the increase in the ratio of the intensity of the beam to the pressure in the neutron tube, resulting from the multicellular source structure of the invention can be exploited in various ways: - With an identical ion path, the creations of ion / electron pairs on the path of the ion beam are less numerous and the energy deposited in the ion source by the re-accelerated electrons is less; the heating of the ion source is lower and consequently the degassing of the constituent materials is reduced. The heavy ions resulting from this degassing are less numerous and their contribution to the erosion of the target weaker. Furthermore, the average energy of the deuterium-tritium ions is increased, which can make it possible to reduce the tube current.
- the maximum current in pulsed mode can be increased in the ratio of pressures Pmax / P, Pmax being the maximum operating pressure not causing a change in the speed of tube operation (passage of the discharge in arc mode).
- Pmax being the maximum operating pressure not causing a change in the speed of tube operation (passage of the discharge in arc mode).
- the distribution of the current on the target is much more homogeneous due on the one hand to the homogeneity of the discharge at the level of the emission channels and on the other hand to the multiplication of the number of elementary beams. This results in a decrease in the maximum ion density and at the same beam current an increase in lifetime.
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- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
- Plasma & Fusion (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Particle Accelerators (AREA)
- Electron Sources, Ion Sources (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8813187 | 1988-10-07 | ||
FR8813187A FR2637726A1 (fr) | 1988-10-07 | 1988-10-07 | Tube neutronique scelle equipe d'une source d'ions multicellulaire a confinement magnetique |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0362947A1 true EP0362947A1 (de) | 1990-04-11 |
EP0362947B1 EP0362947B1 (de) | 1995-04-26 |
Family
ID=9370794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89202465A Expired - Lifetime EP0362947B1 (de) | 1988-10-07 | 1989-10-02 | Mit einer multizellulären Ionenquelle mit magnetischem Einschluss versehene abgeschmolzene Neutronenröhre |
Country Status (5)
Country | Link |
---|---|
US (1) | US5078950A (de) |
EP (1) | EP0362947B1 (de) |
JP (1) | JP2825025B2 (de) |
DE (1) | DE68922364T2 (de) |
FR (1) | FR2637726A1 (de) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0473233A1 (de) * | 1990-08-31 | 1992-03-04 | Societe Anonyme D'etudes Et Realisations Nucleaires S.O.D.E.R.N. | Hochfluss-Neutronenröhre |
EP0645947A1 (de) | 1993-09-29 | 1995-03-29 | Societe Anonyme D'etudes Et Realisations Nucleaires - Sodern | Neutronenröhre mit magnetischem Elektroneneinschluss durch Dauermagneten und dessen Herstellungsverfahren |
US6441569B1 (en) | 1998-12-09 | 2002-08-27 | Edward F. Janzow | Particle accelerator for inducing contained particle collisions |
WO2021091399A1 (en) | 2019-11-06 | 2021-05-14 | Kando Innovation Limited | Productivity enhancement apparatus for power operated skinning equipment |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3122081B2 (ja) * | 1998-11-25 | 2001-01-09 | 石油公団 | 中性子発生管 |
US20100301196A1 (en) * | 2007-05-02 | 2010-12-02 | Wei-Kan Chu | portable/mobile fissible material detector and methods for making and using same |
US8891721B1 (en) | 2011-03-30 | 2014-11-18 | Sandia Corporation | Neutron generators with size scalability, ease of fabrication and multiple ion source functionalities |
CN102243900A (zh) * | 2011-06-28 | 2011-11-16 | 中国原子能科学研究院 | 一种核反应堆启动用一次中子源部件 |
CN102709140B (zh) * | 2012-05-23 | 2014-09-17 | 四川大学 | 一种用于中子管的气体放电型离子源 |
RU2634483C1 (ru) * | 2016-12-09 | 2017-10-31 | Федеральное государственное бюджетное научное учреждение "Федеральный исследовательский центр Институт прикладной физики Российской академии наук" (ИПФ РАН) | Источник нейтронов ограниченных размеров для нейтронной томографии |
IL281747B2 (en) | 2021-03-22 | 2024-04-01 | N T Tao Ltd | System and method for creating plasma with high efficiency |
RU209936U1 (ru) * | 2021-11-24 | 2022-03-24 | Федеральное Государственное Унитарное Предприятие "Всероссийский Научно-Исследовательский Институт Автоматики Им.Н.Л.Духова" (Фгуп "Внииа") | Импульсный нейтронный генератор |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2806161A (en) * | 1952-07-08 | 1957-09-10 | Jr John S Foster | Coasting arc ion source |
LU46217A1 (de) * | 1963-06-12 | 1964-08-01 | ||
NL7707357A (en) * | 1977-07-04 | 1979-01-08 | Philips Nv | Anode for neutron generator ion source - has holes aligned to outlets in cathode converging beams on target |
EP0036665A1 (de) * | 1980-03-26 | 1981-09-30 | Kabushiki Kaisha Toshiba | Ionengenerator |
US4447773A (en) * | 1981-06-22 | 1984-05-08 | California Institute Of Technology | Ion beam accelerator system |
GB2136328A (en) * | 1983-02-17 | 1984-09-19 | Marconi Co Ltd | A method of making a grid |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB980947A (en) * | 1961-06-30 | 1965-01-20 | Atomic Energy Authority Uk | Neutron generator |
DE1303276B (de) * | 1964-08-18 | Philips Nv | ||
JPS594819B2 (ja) * | 1975-10-08 | 1984-02-01 | 双葉電子工業株式会社 | イオン源 |
FR2550681B1 (fr) * | 1983-08-12 | 1985-12-06 | Centre Nat Rech Scient | Source d'ions a au moins deux chambres d'ionisation, en particulier pour la formation de faisceaux d'ions chimiquement reactifs |
-
1988
- 1988-10-07 FR FR8813187A patent/FR2637726A1/fr not_active Withdrawn
-
1989
- 1989-10-02 EP EP89202465A patent/EP0362947B1/de not_active Expired - Lifetime
- 1989-10-02 DE DE68922364T patent/DE68922364T2/de not_active Expired - Fee Related
- 1989-10-04 US US07/416,811 patent/US5078950A/en not_active Expired - Fee Related
- 1989-10-06 JP JP1260309A patent/JP2825025B2/ja not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2806161A (en) * | 1952-07-08 | 1957-09-10 | Jr John S Foster | Coasting arc ion source |
LU46217A1 (de) * | 1963-06-12 | 1964-08-01 | ||
NL7707357A (en) * | 1977-07-04 | 1979-01-08 | Philips Nv | Anode for neutron generator ion source - has holes aligned to outlets in cathode converging beams on target |
EP0036665A1 (de) * | 1980-03-26 | 1981-09-30 | Kabushiki Kaisha Toshiba | Ionengenerator |
US4447773A (en) * | 1981-06-22 | 1984-05-08 | California Institute Of Technology | Ion beam accelerator system |
GB2136328A (en) * | 1983-02-17 | 1984-09-19 | Marconi Co Ltd | A method of making a grid |
Non-Patent Citations (1)
Title |
---|
REVUE DE PHYSIQUEAPPLIQUEE, vol. 12, no. 12, décembre 1977, pages 1835-1848; C. LEJEUNE et al.: "Multiduoplasmatron et multiduopigatron : sources de plasma uniforme pour la formation de faisceaux d'ions multiamperes" * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0473233A1 (de) * | 1990-08-31 | 1992-03-04 | Societe Anonyme D'etudes Et Realisations Nucleaires S.O.D.E.R.N. | Hochfluss-Neutronenröhre |
FR2666477A1 (fr) * | 1990-08-31 | 1992-03-06 | Sodern | Tube neutronique a flux eleve. |
EP0645947A1 (de) | 1993-09-29 | 1995-03-29 | Societe Anonyme D'etudes Et Realisations Nucleaires - Sodern | Neutronenröhre mit magnetischem Elektroneneinschluss durch Dauermagneten und dessen Herstellungsverfahren |
FR2710782A1 (fr) * | 1993-09-29 | 1995-04-07 | Sodern | Tube neutronique à confinement magnétique des électrons par aimants permanents et son procédé de fabrication. |
US5745537A (en) * | 1993-09-29 | 1998-04-28 | U.S. Philips Corporation | Neutron tube with magnetic confinement of the electrons by permanent magnets and its method of manufacture |
US6441569B1 (en) | 1998-12-09 | 2002-08-27 | Edward F. Janzow | Particle accelerator for inducing contained particle collisions |
WO2021091399A1 (en) | 2019-11-06 | 2021-05-14 | Kando Innovation Limited | Productivity enhancement apparatus for power operated skinning equipment |
Also Published As
Publication number | Publication date |
---|---|
EP0362947B1 (de) | 1995-04-26 |
JP2825025B2 (ja) | 1998-11-18 |
DE68922364T2 (de) | 1995-12-14 |
JPH02276198A (ja) | 1990-11-13 |
DE68922364D1 (de) | 1995-06-01 |
US5078950A (en) | 1992-01-07 |
FR2637726A1 (fr) | 1990-04-13 |
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