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    • 33. 发明公开
    • MASS ANALYSER AND METHOD OF MASS ANALYSIS
    • MERANANYSYSOR UND VERFAHREN ZUR MASSENANALYSE
    • EP2681759A1
    • 2014-01-08
    • EP11764713.1
    • 2011-09-28
    • Shimadzu Corporation
    • DING, LiSUDAKOV, MikhailKUMASHIRO, Sumio
    • H01J49/42H01J49/02
    • H01J49/027H01J49/0031H01J49/061H01J49/406H01J49/408H01J49/4245
    • An electrostatic ion trap for mass analysis includes a first array of electrodes and a second array of electrodes, spaced from the first array of electrode. The first and second arrays of electrodes may be planar arrays formed by parallel strip electrodes or by concentric, circular or part-circular electrically conductive rings. The electrodes of the arrays are supplied with substantially the same pattern of voltage whereby the distribution of electrical potential in the space between the arrays is such as to reflect ions isochronously in a flight direction causing them to undergo periodic, oscillatory motion in the space, focused substantially mid-way between the arrays. Amplifier circuitry is used to detect image current having frequency components related to the mass-to-charge ratio of ions undergoing the periodic, oscillatory motion.
    • 用于质量分析的静电离子阱包括第一电极阵列和与第一电极阵列间隔开的第二电极阵列。 第一和第二电极阵列可以是由平行条形电极或同心圆形或部分圆形导电环形成的平面阵列。 阵列的电极被提供有基本相同的电压图案,由此阵列之间的空间中的电位分布使得在飞行方向上等离子地反射离子,使得它们在空间中经历周期性的振荡运动 基本上位于阵列之间。 放大器电路用于检测具有与经历周期性振荡运动的离子的质荷比相关的频率分量的图像电流。
    • 34. 发明公开
    • MASS SPECTROMETRY METHOD AND DEVICE FOR IMPLEMENTING SAME
    • 马萨诸塞州立大学杜塞尔多夫实验室
    • EP2615622A2
    • 2013-07-17
    • EP11803847.0
    • 2011-07-08
    • Saparqaliyev, Aldan Asanovich
    • SAPARQALIYEV, Yerbol Aldanovich
    • H01J49/40G01N30/72
    • H01J49/405G01N30/72H01J49/406H01J49/408
    • The invention relates to an electronic analytical technique for determining the composition and structure of substances and, more specifically, to the field of analyzers comprising at least one mass spectrometer, and can be used in medicine, biology, the oil and gas industry, metallurgy, power engineering, geochemistry, hydrology and ecology. The technical result is that of increasing the resolving power of the mass spectrometer and the sensitivity, accuracy and speed with which the composition and structure of substances are measured, while at the same time increasing the functional capabilities and reducing the geometric dimensions and the mass of substance analyzers. In the mass spectrometry method, an ion flux is generated and controlled using a single-flux, off-axis method; in parallel, using a multi-flux method; using a three-dimensional field with a middle meridian surface, including a reflecting three-dimensional type and a reflecting two-zone type, or using multiple reflection arrays. Embodiments of devices for implementing the method are proposed, as are principle ion optical systems which make it possible to produce different types of mass spectrometers with lower material consumption and smaller geometric dimensions.
    • 本发明涉及一种用于确定物质的组成和结构的电子分析技术,更具体地涉及包括至少一种质谱仪的分析仪领域,并且可以用于医药,生物学,石油和天然气工业,冶金, 电力工程,地球化学,水文和生态学。 技术结果是提高了质谱仪的分辨率,测量物质组成和结构的灵敏度,精度和速度,同时增加了功能性能,降低了几何尺寸和质量 物质分析仪 在质谱法中,使用单通量离轴法生成离子通量并进行控制; 并行使用多通量法; 使用具有中间子午线表面的三维场,包括反射三维型和反射两区型,或使用多个反射阵列。 提出了用于实现该方法的装置的实施例,原理离子光学系统也可以生产具有较低材料消耗和较小几何尺寸的不同类型的质谱仪。
    • 37. 发明授权
    • TANDEM TIME OF FLIGHT MASS SPECTROMETER AND METHOD OF USE
    • TANDEM FLUZEITMASSENSPEKTROMETER和程序
    • EP1522087B1
    • 2011-03-09
    • EP03726518.8
    • 2003-04-29
    • LECO CORPORATION
    • VERENTCHIKOV, Anatoli, N.
    • H01J49/40
    • H01J49/406H01J49/004
    • To provide comprehensive (i.e. rapid and sensitive) MS-MS analysis, the inventor employs a time-nested separation, using two time-of-flight (TOF) mass spectrometers. Parent ions are separated in a slow and long TOF1, operating at low ion energy (1 to l00eV), and fragment ions are mass analyzed in a fast and short TOF2, operating at much higher keV energy. Low energy fragmentation cell between TOF1 and TOF2 is tailored to accelerate fragmentation and dampening steps, mostly by shortening the cell and employing higher gas pressure. Since separation in TOF1 takes milliseconds and mass analysis in TOF2- microseconds, the invention provides comprehensive MS-MS analysis of multiple precursor ions per single ion pulse. Slow separation in TOF1 becomes possible with an introduction of novel TOF1 analyzers. The TOF-TOF could be implemented using a static TOF1, here described on the examples of spiratron, planar and cylindrical multi-pass separators with griddles spatial focusing ion mirrors. Higher performance is expected with the use of novel hybrid TOF 1 analyzers, combining radio frequency (RF) and quadratic DC fields. RF field retains low-energy ions within TOF 1 analyzer, while quadratic DC field improves resolution by compensate for large relative energy spread.