| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 核素转换方法及核素转换装置 | CN201380007232.3 | 2013-01-29 | CN104081467A | 2014-10-01 | 岩村康弘; 伊藤岳彦; 牟田研二; 鹤我薰典 |
| 本发明提供一种核素转换装置及核素转换方法，与加速器或反应堆等大规模的装置相比，能够以规模相对较小的装置进行核素转换，使核素转换量增大。本发明的核素转换装置具备：结构体(1)、从两侧夹入结构体(1)而配置的氘高浓度部(2)及氘低浓度部(3)，向氘高浓度部(2)供给包含重水的电解液(16)，将电解液(16)电解而产生氘，在结构体(1)的氘高浓度部(2)侧的表面附近形成氘浓度高的状态，同时，使氘低浓度部(3)形成氘浓度低于氘高浓度部(2)的状态，使氘从氘高浓度部(2)向氘低浓度部3透过结构体(1)，在结构体(1)中，使实施核素转换的物质在氘的作用下发生核素转换。 | ||||||
| 2 | 核素转换方法及核素转换装置 | CN201380007232.3 | 2013-01-29 | CN104081467B | 2017-03-08 | 岩村康弘; 伊藤岳彦; 牟田研二; 鹤我薰典 |
| 本发明提供一种核素转换装置及核素转换方法，与加速器或反应堆等大规模的装置相比，能够以规模相对较小的装置进行核素转换，使核素转换量增大。本发明的核素转换装置具备：结构体(1)、从两侧夹入结构体(1)而配置的氘高浓度部(2)及氘低浓度部(3)，向氘高浓度部(2)供给包含重水的电解液(16)，将电解液(16)电解而产生氘，在结构体(1)的氘高浓度部(2)侧的表面附近形成氘浓度高的状态，同时，使氘低浓度部从氘高浓度部(2)向氘低浓度部3透过结构体(1)，在结构体(1)中，使实施核素转换的物质在氘的作用下发生核素转换。(3)形成氘浓度低于氘高浓度部(2)的状态，使氘 | ||||||
| 3 | 质子引擎 | CN201180068869.4 | 2011-12-27 | CN103534762B | 2016-04-27 | 欧文·维恩摩尔·罗斯 |
| 一种将物质转换成能量的发电装置。一个螺线管以顺时针方向或逆时针方向以高速圆周地旋转。一个具有类似大小的包含气态或等离子态形式的带电粒子线圈半导体管以相反方向以高速旋转。该中空线圈被缠绕在一个在其内部产生一个磁场的导电线圈内，当一个射频线圈注入一个谐振频率时将这些粒子保持就位以使这些粒子的自旋对齐。这些粒子被以高速率驱入该螺线管的磁场内。收集所产生的能量输出。 | ||||||
| 4 | 核转化方法和核转化装置 | CN201180045124.6 | 2011-07-20 | CN103608869A | 2014-02-26 | 水野忠彦; 石川泰男 |
| 本发明提供了一种核转化方法及其装置，从而可以通过使用简单结构产生热能和氢。利用加热器（6，115），在没有氧的情况下将由诸如SUS304或铁的金属材料形成的反应池（1，100）加热到500°C或更高。然后，将水引入反应池（1，100），以便生成水蒸汽。通过水蒸气和反应池（1，100）的内壁之间的反应，引起核转化，并且产生氢和热能。通过在反应池（1，100）中提供至少包含碱金属和氧的反应剂（NaOH，K2TiO3等），在不使用水的情况下出现核反应。为了激活核反应，水蒸气可以提供到包含反应剂的反应池（1，100）中，并且可以在反应池（1，100）中放置叶片（f）（124）作为金属元素源，以便进一步扩大金属表面。 | ||||||
| 5 | 质子引擎 | CN201180068869.4 | 2011-12-27 | CN103534762A | 2014-01-22 | 欧文·维恩摩尔·罗斯 |
| 一种将物质转换成能量的发电装置。一个螺线管以顺时针方向或逆时针方向以高速圆周地旋转。一个具有类似大小的包含气态或等离子态形式的带电粒子线圈半导体管以相反方向以高速旋转。该中空线圈被缠绕在一个在其内部产生一个磁场的导电线圈内，当一个射频线圈注入一个谐振频率时将这些粒子保持就位以使这些粒子的自旋对齐。这些粒子被以高速率驱入该螺线管的磁场内。收集所产生的能量输出。 | ||||||
| 6 | 高周波振動撹拌のエネルギーと、その撹拌機の振動羽根を両極として水の電気分解により発生するナノ・マイクロバブルの破裂エネルギーの共用で、ある元素から他の元素に変換させる技術及び処理方法、並びに放射性セシウム１３７及び１３４等の放射性物質の無害化する技術及び方法 | JP2013188323 | 2013-09-11 | JP2015055527A | 2015-03-23 | OMASA RYUSHIN |
| 【課題】ある元素から他の元素に変換させる技術及び処理法並びにセシウム134及びセシウム137などの無害化システム及び装置の提供。【解決手段】システムは、処理槽1、高周波振動モーター3、前記モーター3に連結された処理槽1の下方へと伸長する2本の振動棒4及び振動棒4の下部に取付けられた多段式振動羽根5を含んで構成される高周波振動撹拌装置を備えている。前記モーター3を、インバータ6により制御して、処理槽1中の放射性物質を含む液中おいて多段式振動羽根5を100〜200Hzの周波数で振動させることにより、放射性物質の無害化が進行する。更に、多段式振動羽根5を電極と兼用して電気分解することにより、その際発生するナノ・マイクロバブルの破裂により生成する強力なエネルギーにより元素の変換並びに無害化の効果が大幅に向上する。また、この元素変換技術はカルシウムを貴重なコバルトやニッケルへと元素変換することも可能である。【選択図】図1 | ||||||
| 7 | カルシウム、銅、マグネシウム、セシウムなどの元素をより有用な元素に変換する方法及びこの元素変換技術を応用して放射性物質を無害化する方法 | JP2017501624 | 2015-02-25 | JPWO2016135880A1 | 2017-11-30 | 大政 龍晋; 龍晋 大政 |
| 本発明は、処理槽1、処理槽1の上側の台に固定された高周波振動モーター3、前記台に連結された処理槽1の下方へと伸長する2本の振動棒4、及び振動棒4の下部に取付けられた元素変換の触媒となるパラジウム又は白金を表面にメッキした多段式振動羽根5を含んで構成される高周波振動撹拌装置を備え、高周波振動モーター3は、インバータ6により制御されて、処理槽1中の変換すべき元素を含む水溶液2おいて、前記多段式振動羽根5を100〜170Hzの周波数で振動させて水溶液2中の前記元素を別の元素に変換させることを特徴とする方法である。処理すべき溶液に重水を添加すると変換効率が向上する。重水の代わりに、適切な濃度のトリチウム水を添加すると、元素変換を短時間で達成すると同時に放射能汚染の元凶と言われているトリチウム水を有効に利用し、その放射能を減衰又は無害化することができる。 | ||||||
| 8 | Yoko engine | JP2013547604 | 2011-12-27 | JP2014509505A | 2014-04-17 | ヴェンモア ロス，オウェン |
| 物質をエネルギーに変換する発電装置。 ソレノイドが外周上を時計回りまたは反時計回りに高速で回転する。 気体またはプラズマ状の帯電粒子を含む概ね同じ大きさのコイル状半導電管が逆向きに高速で回転する。 中空コイルは内部に磁場を生成する導電コイルに巻かれて、粒子のスピンを整列配置させる共鳴周波数をＲＦコイルが注入する際に、粒子を所定位置に保持する。 粒子は、ソレノイドの磁場内へ高速度で送られる。 その結果生じたエネルギー出力が集められる。
【選択図】図１ |
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| 9 | NUCLEAR TRANSFORMATION METHOD AND NUCLEAR TRANSFORMATION DEVICE | EP11809669 | 2011-07-20 | EP2597652A4 | 2017-11-22 | MIZUNO TADAHIKO; ISHIKAWA YASUO |
| Nuclear transformation method and apparatus can produce thermal energy and hydrogen with a simple structure. A reaction cell 1, 100, made of metal material like iron, from which oxygen is discharged is heated by a heater 6,115 at a temperature above 500°C. Water is supplied into the reaction cell 1,100 to be changed into steam which reacts on the inner wall of the reaction cell 1,100 to produce hydrogen and thermal energy through a nuclear transformation. In the case that a reaction agent (NaOH, K 2 TiO 3 ) which includes at least alkaline metal and oxygen is accommodated in the reaction cell 1,100, a nuclear reaction occurs without the supply of water. Steam may be supplied into the reaction cell 1, 100 to activate the nuclear reaction and fins t 124 as a metal element supplying body may be accommodated in the reaction cell 1,100 to increase the area of the metal surface. | ||||||
| 10 | NUCLIDE CONVERSION METHOD AND NUCLIDE CONVERSION DEVICE | EP13743465.0 | 2013-01-29 | EP2816566B1 | 2017-08-16 | IWAMURA, Yasuhiro; ITOU, Takehiko; MUTA, Kenji; TSURUGA, Shigenori |
| 11 | NUCLIDE CONVERSION METHOD AND NUCLIDE CONVERSION DEVICE | EP13743465 | 2013-01-29 | EP2816566A4 | 2015-09-09 | IWAMURA YASUHIRO; ITOU TAKEHIKO; MUTA KENJI; TSURUGA SHIGENORI |
| 12 | PROTON ENGINE | EP11852655.7 | 2011-12-27 | EP2659491A2 | 2013-11-06 | Ross, Owen Venmore |
| A power generation device that converts matter into energy. A solenoid is rotated circumferentially at high speed clockwise or counter-clockwise. A coiled semi-conductor tube of similar size, which contains charged particles in gas or plasma form is rotated at high speed in the opposite direction. The hollow coil is wrapped in a conducting coil that creates a magnetic field inside it, holding the particles in place as an RF coil injects a resonant frequency to align the spins of the particles. The particles are driven at a high rate of speed into the solenoid's Magnetic field. The resulting energy output is collected. | ||||||
| 13 | Neutron and proton generating processes | US15756982 | 2016-08-01 | US20180261348A1 | 2018-09-13 | Andre Michaud |
| Neutron and proton generating processes consist in a thermal neutrons generation process arising in particular circumstances after destabilization of a coherent electrons beam wherein electrons have a minimum carrying-energy of 1.022 MeV; a thermal protons generation process arising in particular circumstances after destabilization of a coherent positrons beam wherein positrons have a minimum carrying-energy of 1.022 MeV; and a stochastically equal numbers of thermal protons and neutrons generation process arising in particular circumstances after destabilization of a coherent electromagnetic photons beam wherein photons have a minimum energy of 1.022 MeV. Large amounts of residual energy and metastable partons would be produced during each process. | ||||||
| 14 | GENERATOR OF TRANSIENT, HEAVY ELECTRONS AND APPLICATION TO TRANSMUTING RADIOACTIVE FISSION PRODUCTS | US15286354 | 2016-10-05 | US20170040151A1 | 2017-02-09 | Anthony Zuppero; William David Jansen; Craig V. Bishop; Thomas J. Dolan; Paul Crone; William J. Saas |
| Use of adsorption, desorption, particle injection and other means to excite electrons to a region on their band structure diagram near an inflection point were the transient effective mass is elevated proportional to the inverse of curvature. These transient heavy electrons may then cause transmutations similar to transmutations catalyzed by the muons used by Alvarez at UC Berkeley during 1956 in liquid hydrogen. The heavy electrons may also control chemical reactions. | ||||||
| 15 | Least action nuclear processes and materials | US14544169 | 2014-12-03 | US20160322119A1 | 2016-11-03 | Daniel S. Szumski |
| Methods for loading hydrogen and hydrogen isotopes into a metal hydride lattice are described. Additionally, methods for using such a lattice to stimulate nuclear transformations, whether for energy production, specific isotope production or specific isotope consumption are described. Further, compositions of matter for use in these methods are described. | ||||||
| 16 | NUCLIDE TRANSMUTATION METHOD AND NUCLIDE TRANSMUTATION DEVICE | US14374483 | 2013-01-29 | US20150030115A1 | 2015-01-29 | Yasuhiro Iwamura; Takehiko Itou; Kenji Muta; Shigenori Tsuruga |
| A nuclide transmutation device and method which enable nuclide transmutation to be performed in a small-scale device compared with large-scale devices are disclosed. The device comprises a structure, and high and low deuterium concentration units are disposed on either side of the structure so as to sandwich the structure therebetween, wherein an electrolytic solution containing heavy water is supplied to the high deuterium concentration unit and is electrolyzed to generate deuterium, thereby producing a state of high deuterium concentration near the high deuterium concentration unit side surface and placing the low deuterium concentration unit in a state of low deuterium concentration relative to the high deuterium concentration unit, causing the deuterium to penetrate through the structure from the high deuterium concentration unit toward the low deuterium concentration unit, and subjecting a substance to nuclide transmutation by reaction with the deuterium. | ||||||
| 17 | Apparatus and method for automatic preparation of 188 Re-perrhenate solution | US10846658 | 2004-05-17 | US20050255010A1 | 2005-11-17 | Ai-Ren Lo; Bor-Tsung Hsieh; Tseng-Chung Huang; Tsai-Yueh Luo |
| An apparatus includes: a fully automated concentrator for 188Re-Perrhenate solution, a control box, and a control computer. The concentrator is controlled by the control box which obtains the signals from the computer. The operator can control it from far away, and monitor the processes such as liquid transfer, washing, filtration, collection etc. from a monitor for the computer. The apparatus can measure the radioactive activities of the collected concentrated 188Re-perrhenate solution and waste during operation; and can also measure the weights of the collecting bottle and solution. Hence the product quality and working efficiency can be increased, and radiation absorbed dose of an operator can be reduced. | ||||||
| 18 | SYSTEMS TO GENERATE TRANSIENT, ELEVATED EFFECTIVE MASS LECTRON QUASIPARTICLES FOR TRANSMUTING RADIOACTIVE FISSION PRODUCTS AND RELATED METHODS | US15973231 | 2018-05-07 | US20180254116A1 | 2018-09-06 | Anthony Zuppero; Thomas J. Dolan |
| Some embodiments include systems to generate transient, elevated effective mass electron quasiparticles for transmuting radioactive fission products. Other embodiments of related systems and methods also are disclosed. | ||||||
| 19 | DEVICE AND METHOD FOR PRODUCING NEUTRONS | US15748011 | 2016-07-22 | US20180218799A1 | 2018-08-02 | Arash MOFAKHAMI |
| The invention relates to a method for producing and/or capturing neutrons, including the following steps: a) exposing nuclei selected among protons, deuterons and/or tritons to an electric field in order to extract said nuclei and to direct said nuclei thus extracted towards a target (20) containing free electrons; b) for example, exposing said nuclei to a spatial and/or temporal gradient of a first magnetic field so as to give a predefined orientation to the magnetic moments of the nuclei; c) either exposing the target to a second magnetic field so as to give a predefined orientation to the magnetic moments of the free electrons of the target; d) or using an electron-donor superparamagnetic material so that the electrons of the free layers of these materials are oriented in preferred directions generated by the orientation of the resulting magnetic moment of the superparamagnetic material; e) for example, in the case of using a superparamagnetic material, not exposing the proton beam and/or the target to the external magnetic fields. A heating device and/or a device for generating magnetic fields may be required in order to activate the superparamagnetic properties of the material. | ||||||
| 20 | METAL OXYGEN FUSION REACTOR | US15334239 | 2016-10-25 | US20170117066A1 | 2017-04-27 | Kenneth N. Swartz; Gary Rodriguez; Roger X. Lenard; David G Schrunk |
| An exothermic fusion reactor is described that uses metal-oxygen transmutation. The process comprises a negatively-charged environment; a moderator comprising at least one noble gas; a metal, including isotopes of hydrogen; and a facilitator comprising at least one element selected from the group consisting of oxygen, carbon, nitrogen, fluorine, phosphorus, sulfur, chlorine, selenium, bromine, iodine, or combinations thereof. | ||||||
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