CN104378905A - High current neutron generating device - Google Patents
High current neutron generating device Download PDFInfo
- Publication number
- CN104378905A CN104378905A CN201410437059.7A CN201410437059A CN104378905A CN 104378905 A CN104378905 A CN 104378905A CN 201410437059 A CN201410437059 A CN 201410437059A CN 104378905 A CN104378905 A CN 104378905A
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- CN
- China
- Prior art keywords
- deuterium
- ion source
- target
- microwave
- 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.)
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- 229910052805 deuterium Inorganic materials 0.000 claims abstract description 27
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims abstract description 22
- 229910052722 tritium Inorganic materials 0.000 claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims abstract description 7
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000010884 ion-beam technique Methods 0.000 claims abstract description 4
- 239000007789 gas Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 7
- 239000003463 adsorbent Substances 0.000 claims 1
- 150000002500 ions Chemical class 0.000 abstract description 28
- -1 deuterium ions Chemical class 0.000 abstract description 2
- 239000007787 solid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 230000004992 fission Effects 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000003947 neutron activation analysis Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229910052686 Californium Inorganic materials 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- HGLDOAKPQXAFKI-UHFFFAOYSA-N californium atom Chemical compound [Cf] HGLDOAKPQXAFKI-UHFFFAOYSA-N 0.000 description 1
- HGLDOAKPQXAFKI-OUBTZVSYSA-N californium-252 Chemical compound [252Cf] HGLDOAKPQXAFKI-OUBTZVSYSA-N 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000005658 nuclear physics Effects 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
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- Particle Accelerators (AREA)
Abstract
The invention relates to a device for generating and accelerating deuterium ions through a microwave ion source and generating high current neutrons through deuterium and deuterium (deuterium and tritium) reactions. A solid body with the quite high hydrogen absorbing ability is installed on the upper face of a subcooling target, deuterium is ionized by the microwave ion source and then accelerated to own quite high energy to be shot on the target, the high-energy ions shot on the target react with the deuterium adsorbed on the target, and the neutrons are generated. Compared with a penning ion source scheme commonly adopted at present, the size of the device is increased slightly, while the intensity of deuterium ion beam is increased by several times to dozens of times, the output of the neutrons is multiplied, in addition, the service life of the microwave ion source is long, and thus the service life of the whole device can be several years.
Description
Technical field
The present invention relates to the device that a kind of deuterium deuterium (or deuterium tritium) reaction produces neutron, be mainly used in neutron correlative study, as directions such as flaw detection, material analysiss, relate to the aspects such as nuclear physics, material analysis, mineral prospecting.
Background technology
Neutron is a kind of electroneutral particle, has the quality that proton is identical, and it plays the part of in a lot of nuclear reaction important role, and many nucleic can capture neutron, production activation products, and then releases Υ ray, and it is the basis of neutron activation analysis.Neutron activation analysis plays an important role containing in the detection etc. of quantitative analysis, security protection explosive at the exploration of the multiple resources such as oil, material element.
The free neutron half-life shorter (10 minutes 11 seconds), therefore can only now-making-now-using.In the lab, the nucleic of release neutron when the most frequently used neutron source is some decay.Such as the spontaneous fission of californium-252 (half-life is 2.65), has in 100 atoms during 3 californium nuclear fissions and can discharge neutron, and each fission on average can produce 3.7 neutrons; The direct neutron produced by nuclear reactor is also had to draw, for relevant research.The former is expensive, and the latter only could obtain in some specific places.
Adopt ion source to accelerate deuterium ion to carry out deuterium deuterium alpha reaction or deuterium-tritium reaction to obtain neutron be a kind of cheap, safe and reliable method, current this device adopts Penning ion source usually, and mainly due to it, to have volume little, the simple feature of structure.But this ion source life is lower, the ion beam of generation is very little, and maximum only have hundreds of microampere, and for some experiment or analytical work, efficiency is very low.The present invention adopts microwave ion source as the generation of neutron generator ion and accelerator, and draw the particle beams and can reach tens to milliampere up to a hundred, neutron generation efficiency improves greatly.
Summary of the invention
The invention provides a kind of relative low price, safe and reliable high current neutron generating means.
The technical solution used in the present invention is:
1) device adopts totally-enclosed structure, and the devices such as microwave ion source main body, water-cooled hydrogen adsorption target, turbomolecular pump and the external world all do not have gas exchanges.
2), during work, ion source produces and ion is accelerated to very high-energy, gets on low-temperature rotary deuterium body absorbing target.These energetic ions, have part and react with the gas that adsorbs on workpiece target, produce neutron.Ion also has some deuteriums (or tritium) gas and releases while getting to and target producing neutron, the gas of releasing is inhaled into molecular pump, microwave ion source is entered from molecular pump steam vent, become ion again, so both ensure the concentration of microwave ion source gas, can ensure that again vacuum chamber is in good vacuum environment.
3) work after certain hour, can vacuum structure be opened when deuterium concentration reduces or in vacuum chamber, vacuum degree is reduced to certain level, change suction tray and again obtain vacuum environment.
4) the present invention also may be used for deuterium-tritium reaction.
5) the present invention also can adopt conventional vacuum to obtain structure, but gas consumption is larger.
accompanying drawing explanation
Fig. 1 is the structural representation of high current neutron generating means of the present invention.
Embodiment
Embodiment 1:
1) as shown in Figure 1, vacuum cavity 1 is cylindrical, diameter 300mm, and microwave ion source 2 is arranged on its top, disalignment, installation site 70mm.Low temperature deuterium adsorption target 3 is arranged on vacuum cavity 1 bottom centre position, and it is rotated by magnetic seal transmission, and inside is connected with cooling fluid cooling.
2) minute pump 4 is connected to above vacuum cavity 1 by 90 degree of bend pipes, and the steam vent of molecular pump connects the air inlet of microwave ion source 2 by gas pipeline 3, the gas of discharge enters ion source again, in ion source, become ion, again injects.
3) the hydrogen Auto-regulator of a cryogenic absorption target 5 with material is equipped with in gas pipeline 3 inside, by the heating and cooling outside gas pipeline 3, the vacuum degree in adjustment vacuum chamber 1 and the air inflow of microwave ion source 2.When neutron generator initialization, in vacuum cavity 1, vacuum degree is high, and molecular pump 4 Exhaust Gas is less, when entering microwave source 3 gas deficiency by gas pipeline 3, to regulating block heating, produces hydrogen, ion source is normally worked.When equipment works long hours, low temperature deuterium adsorption target 5 release gas more time, to regulating block cooling, make its adsorbed hydrogen, under making ion source be operated in more stable air pressure environment.
4) as shown in Figure 1, microwave ion source 2 is placed with cryogenic absorption target 5 bias, microwave ion source 2 extraction system employing defocused design, divergence of ion beam, can prevent from bombarding rear workpiece target local temperature too high; And in injection process, low temperature deuterium adsorption target 5 constantly rotates, change injection phase, make it irradiate evenly.
The present invention is compared with conventional penning source neutron generator, and longer service life, and its height of the yield ratio of neutron about two orders of magnitude, have very high economic worth.
Claims (6)
1. adopt microwave ion source produce and accelerate a deuterium ion, utilize deuterium deuterium (or deuterium tritium) to react the device producing high current neutron.As shown in Figure 1, deuterium (or tritium) is adsorbed on above sub-cooled target, produces deuterium ion by microwave ion source, accelerates to get on cooled target, deuterium (or tritium) the atom generation nuclear reaction of adsorbing with cooled target, produce neutron through high pressure.
2. method according to right 1, microwave ion source adopts 2.45GHz microwave, and magnetic field is produced by permanent magnet or solenoid coil.
3. method according to right 1, deuterium is adsorbed on above target, target body sub-cooled.
4. method according to right 1, sub-cooled dish is circular, can around its central rotation, and deuterium ion bundle is to its eccentric irradiation.
5. method according to right 1, in order to reduce gas consumption, the overall totally-enclosed design of this neutron generating means, in order to improve microwave ion source ion beam current, the built-in miniature molecular pump of equipment, extracting vacuum indoor gas, then sends into ion source, gas circulation uses, and can keep vacuum house vacuum.
6. method according to right 1, the hydrogen adsorbent that ion source in gas built in pipeline temperature can regulate, regulates for the vacuum degree in ion source and vacuum chamber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN201410437059.7A CN104378905A (en) | 2014-08-29 | 2014-08-29 | High current neutron generating device |
Applications Claiming Priority (1)
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---|---|---|---|
CN201410437059.7A CN104378905A (en) | 2014-08-29 | 2014-08-29 | High current neutron generating device |
Publications (1)
Publication Number | Publication Date |
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CN104378905A true CN104378905A (en) | 2015-02-25 |
Family
ID=52557464
Family Applications (1)
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CN201410437059.7A Pending CN104378905A (en) | 2014-08-29 | 2014-08-29 | High current neutron generating device |
Country Status (1)
Country | Link |
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CN (1) | CN104378905A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104918403A (en) * | 2015-06-26 | 2015-09-16 | 中国工程物理研究院核物理与化学研究所 | Pulsed neutron generator |
CN108269639A (en) * | 2018-01-12 | 2018-07-10 | 中国科学院合肥物质科学研究院 | A kind of high current stable state neutron generation device |
WO2023185219A1 (en) * | 2022-03-31 | 2023-10-05 | 戴文韬 | Nuclear fusion method and device for hydrogen-deuterium-tritium alloy reactor |
Citations (8)
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---|---|---|---|---|
EP0059668B1 (en) * | 1981-03-02 | 1985-10-30 | Commissariat à l'Energie Atomique | High energy neutron generator |
US5215703A (en) * | 1990-08-31 | 1993-06-01 | U.S. Philips Corporation | High-flux neutron generator tube |
CN2775829Y (en) * | 2004-12-30 | 2006-04-26 | 吉林省科仑辐射技术开发有限公司 | High-yield rate neutron tube |
US20100202580A1 (en) * | 2009-01-28 | 2010-08-12 | Los Alamos National Security, Llc | Method and apparatus for neutron generation using liquid targets |
CN101916607A (en) * | 2010-07-28 | 2010-12-15 | 北京大学 | A Small Neutron Source Using a Windowless Gas Target |
WO2013084004A1 (en) * | 2011-12-09 | 2013-06-13 | University Of Lancaster | Neutron source |
JP2014044214A (en) * | 2008-05-02 | 2014-03-13 | Shine Medical Technologies Inc | Device and method for producing medical isotopes |
CN103813611A (en) * | 2014-02-25 | 2014-05-21 | 中国工程物理研究院核物理与化学研究所 | Small directional high-flux neutron generator |
-
2014
- 2014-08-29 CN CN201410437059.7A patent/CN104378905A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0059668B1 (en) * | 1981-03-02 | 1985-10-30 | Commissariat à l'Energie Atomique | High energy neutron generator |
US5215703A (en) * | 1990-08-31 | 1993-06-01 | U.S. Philips Corporation | High-flux neutron generator tube |
CN2775829Y (en) * | 2004-12-30 | 2006-04-26 | 吉林省科仑辐射技术开发有限公司 | High-yield rate neutron tube |
JP2014044214A (en) * | 2008-05-02 | 2014-03-13 | Shine Medical Technologies Inc | Device and method for producing medical isotopes |
US20100202580A1 (en) * | 2009-01-28 | 2010-08-12 | Los Alamos National Security, Llc | Method and apparatus for neutron generation using liquid targets |
CN101916607A (en) * | 2010-07-28 | 2010-12-15 | 北京大学 | A Small Neutron Source Using a Windowless Gas Target |
WO2013084004A1 (en) * | 2011-12-09 | 2013-06-13 | University Of Lancaster | Neutron source |
CN103813611A (en) * | 2014-02-25 | 2014-05-21 | 中国工程物理研究院核物理与化学研究所 | Small directional high-flux neutron generator |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104918403A (en) * | 2015-06-26 | 2015-09-16 | 中国工程物理研究院核物理与化学研究所 | Pulsed neutron generator |
CN108269639A (en) * | 2018-01-12 | 2018-07-10 | 中国科学院合肥物质科学研究院 | A kind of high current stable state neutron generation device |
WO2023185219A1 (en) * | 2022-03-31 | 2023-10-05 | 戴文韬 | Nuclear fusion method and device for hydrogen-deuterium-tritium alloy reactor |
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