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    • 4. 发明专利
    • Ionic mobility spectrometer
    • 离子移动光谱仪
    • JP2009146750A
    • 2009-07-02
    • JP2007323171
    • 2007-12-14
    • Hitachi Ltd株式会社日立製作所
    • OKUMURA AKIHIKO
    • H01J49/40G01N27/62
    • G01N27/622
    • PROBLEM TO BE SOLVED: To realize a compact ionic mobility spectrometer with high selectivity. SOLUTION: Air flow is generated inside a drift tube 5 headed from a detector 18 side toward an ion source side, and a first area a1 with a flow speed increasing in a flowing direction, a second area a2 with a constant flow, and a third area a3 with a flow speed decreasing are arranged in turn from an upstream side toward a downstream side of the air flow. Light irradiation mechanisms 51, 52 are provided at the second area for dissociating ion. COPYRIGHT: (C)2009,JPO&INPIT
    • 要解决的问题:实现具有高选择性的紧凑型离子迁移谱仪。 解决方案:在从检测器18侧朝向离子源侧的漂移管5内产生流动,流动速度在流动方向上增加的第一区域a1,具有恒定流量的第二区域a2, 并且从气流的上游侧向下游侧依次排列具有流速减小的第三区域a3。 光照射机构51,52设置在第二区域以离解离子。 版权所有(C)2009,JPO&INPIT
    • 6. 发明专利
    • Ion filter, mass spectrometry system, and ion mobility spectrometer
    • 离子过滤器,质谱系统和离子移动光谱仪
    • JP2009259465A
    • 2009-11-05
    • JP2008104489
    • 2008-04-14
    • Hitachi Ltd株式会社日立製作所
    • OKUMURA AKIHIKO
    • H01J49/40G01N27/62G01N27/68H01J49/06H01J49/10
    • PROBLEM TO BE SOLVED: To provide a technology capable of separating ion to be detected in a gas phase of atmospheric pressure or near it with a simple configuration and introducing it efficiently into a mass spectrometer or ion detector on a post stage, for improved detection precision at an apparatus on post stage. SOLUTION: An hour glass type flow channel, whose cross sectional area gradually decreases and then gradually increases, is configured along the flow direction of the gas containing ion. A potential difference is provided between an electrode arranged at the upper part of the hour glass and the inner wall of the hour glass flow channel as well as between the inner wall of the hour glass flow channel and the electrode arranged at the lower part of the hour glass. Accordingly, the ion having the ion mobility of a predetermined range is converged into the central part of a flow channel for transmission, while the ion having the ion mobility beyond the predetermined range is caused to advance toward the flow channel inner wall for discharge to the outside of the system. COPYRIGHT: (C)2010,JPO&INPIT
    • 要解决的问题:为了提供能够以简单的结构在大气压的气相或其附近分离待检测的离子的技术,并将其有效地引入到后级的质谱仪或离子检测器中,为 提高后级装置的检测精度。

      解决方案:沿着含离子气体的流动方向配置横截面积逐渐减小然后逐渐增加的小时玻璃流路。 在布置在小时玻璃的上部的电极和小时玻璃流道的内壁之间以及时玻璃流路的内壁和布置在小时玻璃的下部的电极之间的电位差 小时玻璃。 因此,具有预定范围的离子迁移率的离子会聚到用于透射的流动通道的中心部分,而具有超过预定范围的离子迁移率的离子被引导朝向流道内壁排放到 在系统之外。 版权所有(C)2010,JPO&INPIT

    • 7. 发明专利
    • Ion mobility spectrometer
    • 离子移动光谱仪
    • JP2009002815A
    • 2009-01-08
    • JP2007164486
    • 2007-06-22
    • Hitachi Ltd株式会社日立製作所
    • OKUMURA AKIHIKOSAKAIRI MINORU
    • G01N27/62
    • PROBLEM TO BE SOLVED: To provide a monitoring device having high selectivity, being a small-sized analyzer dispensing with a vacuum system. SOLUTION: Two kinds of atmospheric pressure ion sources, namely, an atmospheric pressure ion source (non-dissociative atmospheric pressure ion source) for generating mainly molecular weight-related ions and an atmospheric pressure ion source (dissociative atmospheric pressure ion source) for generating mainly dissociated ions, are provided on an ion mobility spectrometer, to thereby provide a switching mechanism between the non-dissociative ion source and the dissociative ion source. A database is provided, wherein characteristic values (an ion mobility or values related thereto) of the molecular weight-related ions generated from the non-dissociative ion source and the dissociated ions generated from the dissociative ion source are registered relative to each measuring object material. When ions agreeing with the database are detected respectively in both modes of the non-dissociative ion source and the dissociative ion source, it is determined that the measuring object material is detected. In this case, existence of the dissociated ions is checked during operation of the non-dissociative ion source, and existence of the molecular weight-related ions is checked reversely during operation of the dissociative ion source, and the result is allowed to contribute to determination, to thereby improve reliability. COPYRIGHT: (C)2009,JPO&INPIT
    • 要解决的问题:提供具有高选择性的监测装置,其是分配真空系统的小型分析仪。 解决方案:两种大气压离子源,即主要产生分子量相关离子的大气压离子源(非离解大气压离子源)和大气压离子源(离解大气压离子源) 用于产生主要离解的离子,提供在离子迁移谱仪上,从而在非离解离子源和离解离子源之间提供切换机制。 提供数据库,其中从非离解离子源产生的分子量相关离子和离解离子源产生的离解离子的特征值(离子迁移率或与其相关的值)相对于每个测量对象物质进行配准 。 当在非离解离子源和离解离子源的两种模式下分别检测到与数据库一致的离子时,确定检测到测量对象物质。 在这种情况下,在非离解离子源的操作期间检查离解的离子的存在,并且在离解离子源的操作期间相反地检查分子量相关离子的存在,并且使结果有助于确定 ,从而提高可靠性。 版权所有(C)2009,JPO&INPIT
    • 8. 发明专利
    • Capillary tube electrophoretic device
    • 毛细管电泳装置
    • JPH11271273A
    • 1999-10-05
    • JP7883398
    • 1998-03-26
    • Hitachi LtdJapan Science & Technology Corp株式会社日立製作所科学技術振興事業団
    • OKUMURA AKIHIKOHIRABAYASHI TSUDOIKOIZUMI HIDEAKI
    • G01N27/447G01N37/00
    • PROBLEM TO BE SOLVED: To improve the resolution by crossing a sample introducing groove to an electrophoretic groove, and regulating the charge quantity of the crossing part inner wall by the potential of an external electrode.
      SOLUTION: A plate member 1 is formed by connecting a first base 11 to a second base 12. The first base 11 has an electrophoretic passage 2 and a sample injecting passage 3 crossing it which are formed on the connecting surface side of the first base 11, and the second base 12 has through-holes 4 for liquid basin which are formed in the position opposed to both ends of each of the electrophoretic passage 2 and the sample injecting passage 3, respectively. A first electrode 21 and a second electrode 22 are formed in the positions opposed to the crossing part of the passages 2, 3 on the first base 11 and the second base 12. A migration liquid is put in the liquid basins on both ends of the passage 2 and one end of the passage 3, and a sample solution is put in the liquid basin on the other end of the passage 3. The electrophoresis is performed in the state where a voltage is applied to the first electrode 21 and the second electrode 22, and a high voltage is applied to both ends of the passage 2 in this state. The components in the sample are separated in the migration passage and detected by an optical method or the like.
      COPYRIGHT: (C)1999,JPO
    • 要解决的问题:通过将样品引入槽交叉到电泳槽来提高分辨率,并且通过外部电极的电位来调节交叉部分内壁的电荷量。 解决方案:通过将第一基座11连接到第二基座12来形成板构件1.第一基座11具有电泳通道2和与其相交的样品注入通道3,其形成在第一基座11的连接表面侧上 并且第二基座12具有分别形成在与电泳通道2和样本注入通道3的两端相对的位置的液槽用贯通孔4。 第一电极21和第二电极22形成在与第一基底11和第二基底12上的通道2,3的交叉部分相对的位置。将迁移液体放置在第二电极21的两端的液体槽中 通道2和通道3的一端,并且将样品溶液放入通道3另一端的液体槽中。在向第一电极21和第二电极施加电压的状态下进行电泳 在这种状态下,在通道2的两端施加高电压。 样品中的组分在迁移通道中分离并通过光学方法等进行检测。
    • 10. 发明专利
    • CHEMICAL ANALYZER
    • JPH1123564A
    • 1999-01-29
    • JP17931897
    • 1997-07-04
    • HITACHI LTD
    • OKUMURA AKIHIKOHIRABAYASHI TSUDOIKOIZUMI HIDEAKI
    • G01N31/22G01N21/78G01N33/18
    • PROBLEM TO BE SOLVED: To improve heating efficiency and make a device compact by temperature-adjusting a part of a passage, and moving the temperature-adjusted portion in conformity to the speed of a fluid. SOLUTION: A sample from a river, a pond, or the water service and a reagent from a reagent container 5 are fed to a sample passage 1 and a reagent passage 2 by pumps 4, 14 respectively, and they are merged at the confluence X and fed to a waste liquid container 13 through a reaction detection passage 3. When the pumps 4, 14 are operated at the constant flow, the mixed liquid flows at the constant speed, and a temperature adjuster 12 is moved at this speed. Reaction proceeds only at the portion of the temperature adjuster 12 and hardly proceeds at the other portion. An absorption photometer 7 shows a peak response, and the chemical oxygen required quantity can be determined from the height of this peak. The heating region is minimized by this method, heating efficiency is improved, and the device can be made compact.