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    • 1. 发明专利
    • Anaerobic treatment system and method
    • 厌氧处理系统和方法
    • JP2014184386A
    • 2014-10-02
    • JP2013060573
    • 2013-03-22
    • Sumitomo Heavy Ind Ltd住友重機械工業株式会社National Institute For Environmental Studies独立行政法人国立環境研究所
    • FUJIMOTO NORIYUKIINABA HIDEKITAMATSUBO KAZUAKI
    • C02F3/28C02F3/10
    • Y02W10/15
    • PROBLEM TO BE SOLVED: To enable early stable operation under a low-temperature condition.SOLUTION: In an anaerobic treatment system 1, a hydrogen fermentation tank 11 is provided, primary treated water W1, which is organic wastewater containing hydrogen and carbon dioxide gas, is produced in the hydrogen fermentation tank 11, secondary treated water W2 obtained by acid production treatment of organic wastewater and/or the primary treated water W1 is produced in an acid production tank 12, and anaerobic treatment tank inflow wastewater W3 comprising the primary treated water W1 and/or the secondary treated water W2 is fed to an anaerobic treatment tank 13. The hydrogen and carbon dioxide gas contained in the primary treated water W1 are used as substrates by anaerobic bacteria having low-temperature resistance to accelerate the growth of the anaerobic bacteria. Consequently, the anaerobic bacteria having low-temperature resistance become dominant in the anaerobic treatment tank 13 to shorten a period required until starting stable operation.
    • 要解决的问题:在低温条件下能够早期稳定运行。解决方案:在厌氧处理系统1中,设置氢发酵罐11,作为含有氢和二氧化碳气体的有机废水的初级处理水W1, 在氢发生槽11中产生,在酸性生产槽12中生产有机废水和/或一次处理水W1的酸处理得到的二次处理水W2,并且包含一次处理水的厌氧处理槽流入废水W3 W1和/或二次处理水W2被供给到厌氧处理槽13.初级处理水W1中所含的氢和二氧化碳气体通过具有耐低温性的厌氧菌作为底物,以加速厌氧生长 菌。 因此,在厌氧处理槽13中具有耐低温性的厌氧菌成为主导,缩短开始稳定运转所需的时间。
    • 2. 发明专利
    • Measuring method and device for substantially continuously measuring concentration of radioactive cesium in discharged water
    • 测量放射性水中放射性浓度的连续测量浓度的测量方法和装置
    • JP2014085163A
    • 2014-05-12
    • JP2012232419
    • 2012-10-19
    • Daiki Ataka Engineering Co Ltdアタカ大機株式会社National Institute For Environmental Studies独立行政法人国立環境研究所
    • TAKANO TAKEHIKONISHIZAKI YOSHIHIKOYAMADA MASATOEBIE YOSHITAKA
    • G01T1/167G01T1/20G01T7/02
    • PROBLEM TO BE SOLVED: To provide a measuring device that substantially continuously measures radioactive concentration of discharged water containing radioactive cesium, and enables the measurement of the radioactive concentration in a short time at an occurrence site of the discharged water, using a portable device.SOLUTION: A measurement device is composed of below-described configuration parts including: an accommodation tank (1) that accommodates the discharged water serving as a measurement object; a passage container (2) through which the discharged water to be measured passes, and which is composed of a main body (2A) and a lid body (2B); a reservoir (3) that temporarily reserves the discharged water to be measured; a tube (4) for introducing the discharged water; pump means (5) for pumping the discharged water; a radioactive cesium-absorbent agent (6); a NaI scintillator detection part (7A); and means (7B) for measuring a detection result and displaying a measurement result. The passage container is a Marinelli beaker that is provided with an opening (22) for introducing measured water near to a bottom part and an opening (23) for overflow at a top part, and further has a dent (21) for receiving the detection part at the bottom part. The measurement device is used by wrapping the passage container with radioactive shield containers (8A and 8B).
    • 要解决的问题:提供一种测量装置,其基本上连续地测量含有放射性铯的排放水的放射性浓度,并且能够使用便携式装置在排出水的发生位置在短时间内测量放射性浓度。 测量装置由以下构成部分构成,包括:容纳用作测量对象物的排出水的容纳箱(1); 被测量的排出水通过的通道容器(2),由主体(2A)和盖体(2B)构成。 一个临时储存被测量排放水的水库(3); 用于引入排出的水的管(4) 用于泵送排出的水的泵装置(5); 放射性铯吸收剂(6); NaI闪烁体检测部(7A); 以及用于测量检测结果并显示测量结果的装置(7B)。 通道容器是Marinelli烧杯,其设置有用于将测量水引入靠近底部的开口(22)和用于在顶部溢出的开口(23),并且还具有用于接收检测的凹陷(21) 部分在底部。 测量装置通过用放射性屏蔽容器(8A和8B)包裹通道容器来使用。
    • 4. 发明专利
    • Method for estimating effect on viviparity programming
    • 估计影响程度的方法
    • JP2010227079A
    • 2010-10-14
    • JP2009081497
    • 2009-03-30
    • National Institute For Environmental Studies独立行政法人国立環境研究所
    • SONE HIDEKONAGANO REIKOOSAKO SEIICHIROMIYAZAKI KOIMANISHI TOORUAKANUMA HIROMI
    • C12N5/07C12N5/10C12N15/09C12Q1/02C12Q1/68
    • PROBLEM TO BE SOLVED: To provide an estimation system for viviparity programming capable of analyzing many specimens conveniently and rapidly.
      SOLUTION: There is disclosed a method for measuring effect on viviparity programming comprising: bringing a microsphere comprising ES cells into contact with a sample; separating the sample from the microsphere; measuring a gene expression level by exposing a part of the microshpere to a neuralizing factor to create a neurosphere precursor and simultaneously by recovering total RNA from a part of residual microshpere; forming a neuronal cell line model in which a cell constituting the neurosphere is differentiated into a mature neurocyte by culturing the obtained neurosphere precursor in a neuralizing medium using a vessel for culturing a neurocyte; and measuring the cell morphology of the obtained neuronal cell line model.
      COPYRIGHT: (C)2011,JPO&INPIT
    • 要解决的问题:提供能够方便快速地分析许多标本的生物计划的估计系统。 解决方案:公开了一种用于测量生物活性程度的影响的方法,包括:使包含ES细胞的微球与样品接触; 将样品与微球分离; 通过将微量部分暴露于神经因子以产生神经球前体并同时通过从残余微量部分中回收总RNA来测量基因表达水平; 形成神经元细胞系模型,其中通过使用培养神经细胞的血管在神经介质中培养获得的神经球前体,将构成神经球的细胞分化为成熟神经细胞; 并测量获得的神经元细胞系模型的细胞形态。 版权所有(C)2011,JPO&INPIT