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    • 1. 发明申请
    • VARIABLE MAGNETIC FLUX-TYPE ROTARY ELECTRIC MACHINE
    • 可变磁通型旋转电机
    • US20150340915A1
    • 2015-11-26
    • US14408977
    • 2012-06-26
    • Takashi KATORobert LORENZNatee LIMSUWAN
    • Takashi KATORobert LORENZNatee LIMSUWAN
    • H02K1/27
    • H02K1/276H02K1/2766H02K1/2773
    • A variable magnetic flux-type rotary electric machine includes a stator and a rotor. The stator includes a stator coil wound on teeth. The rotor defines an air gap between the rotor and the stator. The rotor has at least one permanent magnet arranged in the d-axis magnetic path. The stator and the rotor are arranged relative to the permanent magnet to set a characteristic of d(Kt(I))/dI≧0 in a range of at or below magnetic saturation of a core material of at least one of the stator and the rotor, where KT represents a torque constant, and I represents an applied current, and a function of KT with respect to I is represented by KT=Kt(I) for a torque Tr acting on the rotor that is represented by Tr=KT×I.
    • 可变磁通型旋转电机包括定子和转子。 定子包括缠绕在齿上的定子线圈。 转子限定了转子和定子之间的气隙。 转子具有布置在d轴磁路中的至少一个永磁体。 定子和转子相对于永磁体布置,以在定子和至少一个定子的芯材的磁饱和度或者低于其定子的磁心的范围内设定d(Kt(I))/dI≥0的特性 转子,其中KT表示转矩常数,I表示施加的电流,并且KT对于I的函数由用于由Tr = KT×表示的转子上的扭矩Tr表示为KT = Kt(I) 一世。
    • 2. 发明授权
    • Medical system and method for operating a medical system
    • 医疗系统和操作医疗系统的方法
    • US09101307B2
    • 2015-08-11
    • US13445607
    • 2012-04-12
    • Detlef ThymRobert Lorenz
    • Detlef ThymRobert Lorenz
    • G06K7/01A61B5/151A61B5/145A61B19/00
    • A61B5/14532A61B90/90A61B90/98A61B2090/0814A61B2560/029A61B2562/0247G06F19/00
    • A medical system and method to operating the medical system is presented. A patient storage element is assigned to a patient comprising identification information identifying the patient. A medical device has a contaminating patient application. A medical device storage element on the medical device comprises use information. A clearing device receives the identification information from the patient storage element and the use information from the medical device storage element and analyzes the use information. If in analyzing the use information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted. If in analyzing the use information it is found that application of the medical device to the patient is not allowed, the identification information is analyzed. If in analyzing the identification information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted.
    • 介绍了医疗系统和操作医疗系统的方法。 患者存储元件被分配给患者,包括识别患者的识别信息。 医疗器械具有污染的患者应用。 医疗装置上的医疗装置存储元件包括使用信息。 清除装置从患者存储元件接收识别信息和来自医疗装置存储元件的使用信息,并分析使用信息。 如果在分析使用信息时发现允许将医疗装置应用于患者,则输出间隙信号。 如果在分析使用信息中发现不允许将医疗装置应用于患者,则分析识别信息。 如果在分析识别信息时发现允许将医疗装置应用于患者,则输出间隙信号。
    • 4. 发明授权
    • Analysis system for the photometric determination of an analyte in a body fluid
    • 用于体液中分析物的光度测定的分析系统
    • US08481329B2
    • 2013-07-09
    • US12606361
    • 2009-10-27
    • Ulrich PorschRobert Lorenz
    • Ulrich PorschRobert Lorenz
    • G01N21/00
    • G01N21/8483Y10T436/11
    • The invention relates to an analysis system for the photometric determination of an analyte in a body fluid, having an analysis device and a test carrier. The test carrier has an evaluation zone in which a photometrically detectable change takes place as the result of a reaction of a sample of the body fluid which contacts the test carrier with a reagent contained in the test carrier. The analysis device comprises an optical emitter for emitting light onto the evaluation zone, an optical receiver for receiving light from the evaluation zone and for generating a measurement signal corresponding to the received light, and a measurement and evaluation device with a measuring unit and an evaluating unit. The measurement signal is amplified and digitalized in the measuring unit. In the evaluating unit, the concentration value is determined from the digitalized measurement signal. In the evaluating unit, a control value of a control parameter is detected at one detection point during the processing after the calculation step. An error in the measurement and evaluation device is recognized if the deviation of the control value from the expected value exceeds a predefined threshold value.
    • 本发明涉及一种用于对具有分析装置和测试载体的体液中的分析物进行光度测定的分析系统。 测试载体具有评估区,其中由于与测试载体接触的体液的样品与测试载体中包含的试剂的反应而发生光度可检测的变化。 分析装置包括用于将光发射到评估区域的光发射器,用于接收来自评估区域的光并用于产生对应于所接收的光的测量信号的光接收器,以及具有测量单元和评估装置的测量和评估装置 单元。 测量信号在测量单元中放大和数字化。 在评估单元中,从数字化测量信号确定浓度值。 在评估单元中,在计算步骤之后的处理期间的一个检测点处检测控制参数的控制值。 如果控制值与期望值的偏差超过预定义的阈值,则识别测量和评估装置中的错误。
    • 5. 发明申请
    • Methods and Systems for Pre-Emphasis of an Envelope Tracking Power Amplifier Supply Voltage
    • 信号跟踪功率放大器供电电压预加重的方法和系统
    • US20130109442A1
    • 2013-05-02
    • US13492279
    • 2012-06-08
    • Sriraman DAKSHINAMURTHYRobert LORENZ
    • Sriraman DAKSHINAMURTHYRobert LORENZ
    • H03G3/20H04B1/40
    • H03G3/20H03G3/3047H04B1/40
    • Embodiments provide systems and methods for producing an envelope tracking (ET) PA supply voltage with minimum headroom relative to the desired RF output signal of the PA. In an embodiment, the PA supply voltage is generated by applying an ET signal to an ET path of the wireless device, and by further applying pre-emphasis to the ET signal to compensate for a frequency response of the ET path. Embodiments operate by estimating the frequency response of the ET path and determining the pre-emphasis based on the estimate of the frequency response of the ET path. In embodiments, the pre-emphasis is applied using a pre-emphasis filter, which may be within or outside of the ET path. Further, the pre-emphasis may be applied to the ET signal in digital or analog form.
    • 实施例提供用于产生相对于PA的期望RF输出信号具有最小净空的包络跟踪(ET)PA供电电压的系统和方法。 在一个实施例中,通过将ET信号施加到无线设备的ET路径,并且进一步对ET信号进行预加重以补偿ET路径的频率响应来产生PA供电电压。 实施例通过估计ET路径的频率响应并基于ET路径的频率响应的估计来确定预加重来进行操作。 在实施例中,使用可以在ET路径内或外的预加重滤波器来应用预加重。 此外,预加重可以数字或模拟形式应用于ET信号。
    • 6. 发明申请
    • Medical system and method for operating a medical system
    • 医疗系统和操作医疗系统的方法
    • US20120262274A1
    • 2012-10-18
    • US13445607
    • 2012-04-12
    • Detlef ThymRobert Lorenz
    • Detlef ThymRobert Lorenz
    • G06K7/01A61B5/151
    • A61B5/14532A61B90/90A61B90/98A61B2090/0814A61B2560/029A61B2562/0247G06F19/00
    • A medical system and method to operating the medical system is presented. A patient storage element is assigned to a patient comprising identification information identifying the patient. A medical device has a contaminating patient application. A medical device storage element on the medical device comprises use information. A clearing device receives the identification information from the patient storage element and the use information from the medical device storage element and analyzes the use information. If in analyzing the use information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted. If in analyzing the use information it is found that application of the medical device to the patient is not allowed, the identification information is analyzed. If in analyzing the identification information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted.
    • 介绍了医疗系统和操作医疗系统的方法。 患者存储元件被分配给患者,包括识别患者的识别信息。 医疗器械具有污染的患者应用。 医疗装置上的医疗装置存储元件包括使用信息。 清除装置从患者存储元件接收识别信息和来自医疗装置存储元件的使用信息,并分析使用信息。 如果在分析使用信息时发现允许将医疗装置应用于患者,则输出间隙信号。 如果在分析使用信息中发现不允许将医疗装置应用于患者,则分析识别信息。 如果在分析识别信息时发现允许将医疗装置应用于患者,则输出间隙信号。
    • 9. 发明申请
    • ANALYSIS SYSTEM FOR THE PHOTOMETRIC DETERMINATION OF AN ANALYTE IN A BODY FLUID
    • 体液中分析物的光度测定分析系统
    • US20100075433A1
    • 2010-03-25
    • US12606361
    • 2009-10-27
    • Ulrich PorschRobert Lorenz
    • Ulrich PorschRobert Lorenz
    • G01N21/00
    • G01N21/8483Y10T436/11
    • The invention relates to an analysis system for the photometric determination of an analyte in a body fluid, having an analysis device and a test carrier. The test carrier has an evaluation zone in which a photometrically detectable change takes place as the result of a reaction of a sample of the body fluid which contacts the test carrier with a reagent contained in the test carrier. The analysis device comprises an optical emitter for emitting light onto the evaluation zone, an optical receiver for receiving light from the evaluation zone and for generating a measurement signal corresponding to the received light, and a measurement and evaluation device with a measuring unit and an evaluating unit. The measurement signal is amplified and digitalized in the measuring unit. In the evaluating unit, the concentration value is determined from the digitalized measurement signal. In the evaluating unit, a control value of a control parameter is detected at one detection point during the processing after the calculation step. An error in the measurement and evaluation device is recognized if the deviation of the control value from the expected value exceeds a predefined threshold value.
    • 本发明涉及一种用于对具有分析装置和测试载体的体液中的分析物进行光度测定的分析系统。 测试载体具有评估区,其中由于与测试载体接触的体液的样品与测试载体中包含的试剂的反应而发生光度可检测的变化。 分析装置包括用于将光发射到评估区域的光发射器,用于接收来自评估区域的光并用于产生对应于所接收的光的测量信号的光接收器,以及具有测量单元和评估装置的测量和评估装置 单元。 测量信号在测量单元中放大和数字化。 在评估单元中,从数字化测量信号确定浓度值。 在评估单元中,在计算步骤之后的处理期间的一个检测点处检测控制参数的控制值。 如果控制值与期望值的偏差超过预定义的阈值,则识别测量和评估装置中的错误。