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    • 51. 发明专利
    • Method and device for solidifying radioactive waste
    • 用于固化放射性废物的方法和装置
    • JP2008286525A
    • 2008-11-27
    • JP2007128895
    • 2007-05-15
    • Toshiba Corp株式会社東芝
    • YAMASHITA TAKEOKANEKO MASAAKIHARUGUCHI YOSHIKOMIKURA MICHITAKASATO TATSUAKIKOMATSUBARA MASARU
    • G21F9/30G21F9/16
    • PROBLEM TO BE SOLVED: To provide a method for solidifying radioactive waste and a device therefor which can inhibit inclination of a gas in a container to become flammable due to rise of the pressure in the container or generated hydrogen.
      SOLUTION: The method for solidifying radioactive waste comprises a mixture accommodating step wherein a mixture of radioactive waste containing radionuclide(s) and solidifying material is accommodated in a solidifying container, and a water stability improver adding step wherein a water stability improver is added to the mixture before the mixture is accommodated in the solidifying container, or wherein the water stability improver is added to the solidifying container before or after the mixture is accommodated in the solidifying container. The water stability improver maintains an electric potential at which water can be stable under alkaline conditions in a solidified body obtained by solidifying the mixture.
      COPYRIGHT: (C)2009,JPO&INPIT
    • 要解决的问题:提供一种固化放射性废物的方法及其装置,其可以抑制容器中的气体由于容器或产生的氢气中的压力升高而变得易燃的倾向。 解决方案:固化放射性废物的方法包括混合物容纳步骤,其中将含有放射性核素的放射性废物和固化材料的混合物容纳在固化容器中,以及水稳定性改进剂添加步骤,其中水稳定性改进剂为 在将混合物容纳在固化容器中之前加入到混合物中,或者在将混合物容纳在凝固容器中之前或之后将水稳定性改进剂加入固化容器中。 水稳定性改进剂在通过固化混合物获得的凝固体中保持水在碱性条件下稳定的电位。 版权所有(C)2009,JPO&INPIT
    • 52. 发明专利
    • Nuclide separation method of radioactive waste, nuclide sample production method, and uranium analysis method
    • 放射性废物的核素分离方法,核素样品生产方法和铀分析方法
    • JP2006317290A
    • 2006-11-24
    • JP2005140364
    • 2005-05-12
    • Toshiba Corp株式会社東芝
    • MURATA EIICHIHARUGUCHI YOSHIKOMIKURA MICHITAKASATO KOKICHI
    • G01N1/10G01T1/167G01T7/02
    • PROBLEM TO BE SOLVED: To provide a new separation method of a nuclide included in radioactive waste, and a method for simple uranium quantitative analysis in the radioactive waste.
      SOLUTION: In step S1, hydrofluoric acid aqueous solution wherein the nuclide in the radioactive waste is dissolved is prepared and produced. In step S2, ion-exchange adsorption of the nuclide dissolved in the hydrofluoric acid aqueous solution is performed by using a fluorine-ion type anion-exchange resin. In step S3, the nuclide subjected to the ion-exchange adsorption onto the anion-exchange resin is selectively eluted and separated by a prescribed chemical medical solution. In step S4, the nuclide is subjected to coprecipitation separation by adding, for example, samarium. In step S5, measurement of an α-ray spectrum of a coprecipitate is performed. Thus, for example, identification of an uranium isotope in the radioactive waste and its quantitative analysis can be performed simply.
      COPYRIGHT: (C)2007,JPO&INPIT
    • 要解决的问题:提供放射性废物中包含的核素的新分离方法,以及放射性废物中简单铀定量分析的方法。 解决方案:在步骤S1中,制备并生产放射性废物中的核素溶解的氢氟酸水溶液。 在步骤S2中,使用氟离子型阴离子交换树脂进行溶解在氢氟酸水溶液中的核素的离子交换吸附。 在步骤S3中,经阴离子交换树脂进行离子交换吸附的核素被规定的化学药液选择性地洗脱分离。 在步骤S4中,通过添加例如钐将核素进行共沉淀分离。 在步骤S5中,进行共沉淀物的α射线谱的测定。 因此,例如,可以简单地进行放射性废物中的铀同位素的鉴定及其定量分析。 版权所有(C)2007,JPO&INPIT
    • 53. 发明专利
    • Microchip, apparatus and method for producing hydrogen-producing raw material
    • 微生物,生产氢原料的装置和方法
    • JP2006256872A
    • 2006-09-28
    • JP2005072160
    • 2005-03-15
    • Toshiba Corp株式会社東芝
    • MIZUGUCHI KOJITAKAHASHI RIYOUTAMURAKAMI KAZUOTAKASE HARUHIKONAKAMURA HIDEKIMIKURA MICHITAKAUTSUNOMIYA KAZUHIRO
    • C01B3/02B01J19/00C01B3/04C01B7/14
    • Y02E60/364
    • PROBLEM TO BE SOLVED: To reduce the amount of iodine used in hydrogen production through an IS (Iodine-Sulfur) method wherein water is decomposed by iodine and sulfur dioxide.
      SOLUTION: A microchip for producing a hydrogen-producing raw material is equipped with a plurality of injection microchannels 1a, 1b and 1c through each of which different fluid is injected, a reaction microchannel 2 in which the fluids injected through the injection microchannels 1a, 1b and 1c are combined to produce the hydrogen-producing raw material through a chemical reaction and a plurality of separation microchannesl 3a, 3b and 3c for dividing liquid that comes out from the reaction microchannel 2. The reaction microchannel 2 has separating means 4 along the extensions of boundaries between the injection microchannels 1a, 1b and 1c. The separating means 4 assist separation of the flow inside the reaction microchannel 2 and also allow substantial mixing.
      COPYRIGHT: (C)2006,JPO&NCIPI
    • 要解决的问题:通过碘(二氧化硫)分解水中的IS(碘 - 硫)法减少生产氢的碘量。 解决方案:用于制造生产氢原料的微芯片配备有多个通过注入不同流体的注入微通道1a,1b和1c,反应微通道2,其中通过注射微通道注入的流体 将1a,1b和1c组合起来,通过化学反应制造生产氢的原料,以及多个用于分离从反应微通道2出来的液体的分离微通道3a,3b和3c。反应微通道2具有分离装置4 沿着注射微通道1a,1b和1c之间的边界的延伸。 分离装置4有助于分离反应微通道2内部的流并且还允许大量混合。 版权所有(C)2006,JPO&NCIPI
    • 54. 发明专利
    • 溶質の回収方法および溶質の回収装置
    • 解决方案和解决方案的恢复方法
    • JP2015054282A
    • 2015-03-23
    • JP2013188848
    • 2013-09-11
    • 株式会社東芝Toshiba Corp
    • MIYAMOTO MASAYAIKEI SHUKOKAWAUCHI KANAENAGAMORI YASUHIKOYAMASHITA TAKEOMIKURA MICHITAKA
    • C02F1/62C02F1/58
    • 【課題】重金属およびリンを含有する強酸性の溶液から、重金属類とリンを選択的に回収することが可能な、溶質の回収方法および溶質の回収装置を提供することを目的とする。【解決手段】実施形態の溶質の回収方法は、初期溶液に重金属除去剤を添加する重金属除去ステップと、重金属除去剤が添加された初期溶液を第1の液相と第1の固相に固液分離する第1の固液分離ステップと、第1の液相にリン除去剤を添加するリン除去ステップと、リン除去剤が添加された第1の液相を第2の液相と第2の固相に固液分離する第2の固液分離ステップと、を備え、初期溶液は焼却灰から放射性核種を抽出した後に放射性核種が回収された溶液であるものとする。【選択図】図3
    • 要解决的问题:提供能够从包括重金属和磷的强酸性溶液中选择性地回收重金属和磷的溶质的溶质和回收装置的回收方法。解决方案:实施方案的溶质回收方法 包括将重金属去除剂添加到初始溶液中的重金属去除步骤,将已经添加有重金属去除剂的初始溶液固液分离到第一液相中的第一固液分离步骤和第一 固相,磷除去步骤,向第一液相中加入除磷剂;以及第二固 - 液分离步骤,将已经加入除磷剂的第一液相固液分离到第二液相中, 第二固相; 初始溶液是通过从焚烧灰中提取放射性核素然后回收放射性核素获得的溶液。
    • 57. 发明专利
    • Nuclear reactor operation method and nuclear reactor control apparatus
    • 核反应堆运行方法和核反应堆控制装置
    • JP2013002943A
    • 2013-01-07
    • JP2011134091
    • 2011-06-16
    • Toshiba Corp株式会社東芝
    • KIKUCHI TSUKASAYOSHIOKA KENICHIMIKURA MICHITAKAMATSUYAMA KANAE
    • G21C7/24
    • Y02E30/31Y02E30/39
    • PROBLEM TO BE SOLVED: To suppress a generation amount of Hf182 in a long-lifetime type Hf control rod including hafnium because the H182 generated when hafnium stays for a long period in a nuclear reactor is a nuclide of a long half-life period (9×10years) and it with a daughter nuclide Ta182 emitting high energy γ-ray (1121.3 kev) causes a permanent equilibrium.SOLUTION: In an operation method of a nuclear reactor having multiple long-lifetime type Hf control rods 1 of whose material includes hafnium, concerning the multiple long-lifetime type Hf control rods 1, a part of them are all pulled out because of attenuation of Hf181 which is a precursor of H182 in an intermediate period of a reactor cycle which corresponds to a period starting from a time when a predetermined period has elapsed from the operation start of the reactor cycle until reaching a prescribed time before the operation end in at least one reactor cycle within a use period of the long-lifetime type Hf control rod 1.
    • 待解决的问题:为了抑制包括铪的长寿命型Hf控制棒中的Hf182的产生量,因为在核反应堆中长时间保持铪所产生的H182是长半衰期的核素 周期(9×10 6 年),与发射高能γ射线(1121.3kev)的子核素Ta182导致永久平衡。 解决方案:在具有多种长寿命型Hf控制棒1的材料包括铪的多个长寿命型Hf控制棒1的核反应堆的操作方法中,其一部分全部被拉出,因为 在反应器周期的中间期期间是H182的前体的Hf181的衰减,其对应于从从反应器循环的操作开始经过预定时间直到操作结束之前的规定时间为止的时间段 在长寿命型Hf控制棒1的使用期内的至少一个反应器循环。版权所有(C)2013,JPO&INPIT
    • 58. 发明专利
    • Quantitative analysis method of plutonium
    • 钚的定量分析方法
    • JP2012225663A
    • 2012-11-15
    • JP2011090701
    • 2011-04-15
    • Toshiba Corp株式会社東芝
    • YAMASHITA TAKEOMIKURA MICHITAKAKUROSAWA SETSUMIMURATA EIICHIMATSUYAMA KANAEHARUGUCHI YOSHIKOSAKURAI JIROHIROSE EMIKO
    • G01T1/167
    • PROBLEM TO BE SOLVED: To provide Pu (plutonium) quantitative analysis method capable of quantitatively analyzing Pu by using radiation measurement such as α-ray spectrometry even in an analysis target sample solution containing much impurity elements such as Ca interrupting α-ray measurement.SOLUTION: The Pu quantitative analysis method for quantitatively analyzing Pu in an analysis target sample solution 10 includes: an iron hydroxide coprecipitation step S101 for generating iron hydroxide coprecipitate 12 containing a rare earth element by adding rare earth compound and iron compound to the analysis target sample solution 10; a rare earth fluoride coprecipitation step S104 for generating rare earth fluoride coprecipitate 15 by adding fluoride to an iron hydroxide coprecipitate solution 13 obtained by dissolving the iron hydroxide coprecipitate 12; and a radiation measurement step S107 for quantitatively analyzing Pu by radiation measurement of a measuring sample 16 prepared from the rare earth fluoride coprecipitate 15.
    • 要解决的问题:为了提供能够通过使用诸如α射线光谱法的辐射测量来定量分析Pu的Pu(钚)定量分析方法,即使在含有大量杂质元素如Ca中断α-射线的分析目标样品溶液中 测量。 解决方案:用于在分析对象样品溶液10中定量分析Pu的Pu定量分析方法包括:通过向稀土化合物和铁化合物添加含有稀土元素的氢氧化铁共沉淀物12的氢氧化铁共沉淀步骤S101, 分析目标样品溶液10; 稀土氟化物共沉淀步骤S104,用于通过将氟化氢沉淀物12溶解得到的氢氧化铁共沉淀溶液13中加入氟化物来生成稀土氟化物共沉淀物15; 以及辐射测量步骤S107,用于通过由稀土氟化物共沉淀物15制备的测量样品16的辐射测量来定量分析Pu。(C)2013,JPO和INPIT