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    • 2. 发明申请
    • Real time analyzer and method for analysis
    • 实时分析仪和分析方法
    • US20080128615A1
    • 2008-06-05
    • US11987085
    • 2007-11-27
    • Masuyoshi YamadaMasako Ishimaru
    • Masuyoshi YamadaMasako Ishimaru
    • H01J49/04
    • H01J49/0422
    • An analyzer carrying out analysis with a high degree of qualitative accuracy by separating impurities which hinder the analysis while analyzing in real time. An introducing tube is branched with one branched tube directly leading to an ion source for real time analysis. The other branched tube leads to the ion source so as to introduce the sample gas into the ion source at a later time. When a result of the real time analysis shows that a spectrum pattern on a MS spectrum is changed and an increase in the concentration of an impurity is observed, the introducing path for the sample gas is changed so that the sample gas is introduced into the ion source after the impurity is separated at the separation part.
    • 分析仪通过分析实时分析分析杂质,以高度的定性精度进行分析。 引入管被分支,一个分支管直接通向离子源进行实时分析。 另一个分支管通向离子源,以便稍后将样品气体引入离子源。 当实时分析的结果表明MS谱上的光谱图变化并且观察到杂质浓度增加时,改变样品气体的引入路径,使样品气体被引入离子 杂质在分离部分分离出来。
    • 3. 发明授权
    • Mass spectrometer and method of mass spectrometry
    • 质谱仪和质谱法
    • US08253097B2
    • 2012-08-28
    • US12039762
    • 2008-02-29
    • Masako IshimaruMasuyoshi Yamada
    • Masako IshimaruMasuyoshi Yamada
    • H01J49/00
    • H01J49/168G01N30/461G01N30/7213H01J49/147
    • In a mass spectrometer having ion sources capable of switching between atmospheric pressure chemical ionization and electron impact ionization, a first gas chromatography device capable of separating a sample to meet a condition suitable for atmospheric pressure chemical ionization measurement is connected to upstream of an atmospheric pressure chemical ionization ion source. Part of the sample separated by the first gas chromatography device is introduced to a second gas chromatography device by distributing a flow channel. In the second gas chromatography device, a target substance and background ingredients contained in the sample are further separated and are introduced to an electron impact ionization ion source. By separating the target substance from the background ingredients, an electron impact ionization spectrum of the target substance is obtained without an effect of the background ingredients.
    • 在具有能够在大气压化学电离和电子轰击电离之间切换的离子源的质谱仪中,能够分离样品以满足适于大气压化学电离测量的条件的第一气相色谱装置连接到大气压化学品 电离离子源。 通过分配流动通道将由第一气相色谱装置分离的样品的一部分引入第二气相色谱装置。 在第二气相色谱装置中,将样品中所含的目标物质和背景成分进一步分离并引入电子轰击离子化离子源。 通过将目标物质与背景成分分离,可以获得目标物质的电子轰击电离光谱,而不影响背景成分。
    • 5. 发明申请
    • QUANTITATIVE ANALYSIS METHOD USING MASS SPECTROMETER
    • 使用质谱仪的量化分析方法
    • US20110101215A1
    • 2011-05-05
    • US12921087
    • 2009-03-27
    • Atsumu HirabayashiMasako IshimaruKiyomi YoshinariNaomi Manri
    • Atsumu HirabayashiMasako IshimaruKiyomi YoshinariNaomi Manri
    • H01J49/00
    • G01N30/8675G01N30/7233H01J49/0009
    • In quantitation without using the isotope labeling technique, there is no means to detect the presence/absence and the time region of the occurrence of quantitative analysis-inhibitory factors in data for the analysis, and the reliability of the data for the analysis cannot be evaluated. Also, the error of the data due to the occurrence of the quantitative analysis-inhibitory factors cannot be evaluated. In order to solve the problems, first, an internal standard to be detected simultaneously with a component for the analysis is mixed in a mobile phase or an eluate of a liquid chromatograph; under the condition where no quantitative analysis-inhibitory factors occur, a blank sample is analyzed to acquire a mass chromatogram of ions originated from the internal standard; and the result is stored in a data storage unit. Then, a sample for the analysis is mixed to acquire data for the analysis of the sample; and the intensity of ions originated from the internal standard is compared with that of the blank sample in the analysis real time in a data analysis unit. At this time, if an inconsistency exceeding a predetermined threshold is detected, the occurrence of the quantitative analysis-inhibitory factors can be detected. Further, based on the inconsistency, the error range of the data can be given to a data set and the like.
    • 在不使用同位素标记技术的定量中,无法检测分析数据中定量分析抑制因子的发生的存在/不存在和时间区域,并且不能评估用于分析的数据的可靠性 。 此外,由于定量分析抑制因子的发生导致的数据误差不能被评估。 为了解决上述问题,首先,将与分析用成分同时检测的内标与液相色谱仪的流动相或洗脱液混合, 在没有定量分析抑制因子发生的条件下,分析空白样品以获得源自内标的离子的质谱图; 结果存储在数据存储单元中。 然后,将用于分析的样本混合以获取用于样品分析的数据; 在数据分析单元中实时分析从内部标准产生的离子强度与空白样本的强度进行比较。 此时,如果检测到超过预定阈值的不一致,则可以检测定量分析抑制因子的发生。 此外,基于不一致性,可以向数据集等提供数据的误差范围。