Oxygenate to olefin manufacture and recovery process
    11.
    发明申请
    Oxygenate to olefin manufacture and recovery process 有权
    氧化烯与烯烃的制备和回收过程

    公开(公告)号:US20060135632A1

    公开(公告)日:2006-06-22

    申请号:US11097809

    申请日:2005-04-01

    CPC classification number: C07C1/20 C07C11/02

    Abstract: This invention is directed to methods for forming an olefin stream from a methanol stream. A lower grade methanol, such as chemical grade or crude methanol, can be used as feed to form the olefin stream. The process uses a relatively simple distillation type step to vaporize a portion of the methanol feed stream and send the resulting vapor stream to a reaction unit to form the olefin stream. In addition, the invention provides the ability to operate the downstream recovery units with reduced fouling or plugging due to the presence of fine solids components.

    Abstract translation: 本发明涉及从甲醇流形成烯烃流的方法。 低级甲醇如化学级或粗甲醇可用作进料以形成烯烃流。 该方法使用相对简单的蒸馏步骤来蒸发一部分甲醇进料流并将所得蒸气流送至反应单元以形成烯烃流。 此外,本发明提供了由于存在细固体组分而使下游回收单元具有减少的结垢或堵塞的能力。

    Command queuing for multimedia storage devices
    13.
    发明授权
    Command queuing for multimedia storage devices 有权
    多媒体存储设备的命令排队

    公开(公告)号:US09591112B2

    公开(公告)日:2017-03-07

    申请号:US10335139

    申请日:2002-12-31

    CPC classification number: H04M1/0274 G06F1/16 H04B1/3816 H04L49/90

    Abstract: A multi-media device interface (18) couples a multi-media device (16) to a portable electronic device (10). Multi-media and other information can be loaded into the portable electronic device (10) from the multi-media device (16) or stored in the multi-media device (16) from the portable electronic device (10). The multi-media device interface (18) queues commands to the multi-media device (16) from the portable electronic device (10) while the multi-media device (16) completes a previously-issued command.

    Abstract translation: 多媒体设备接口(18)将多媒体设备(16)耦合到便携式电子设备(10)。 多媒体和其他信息可以从多媒体设备(16)加载到便携式电子设备(10)中或从便携式电子设备(10)存储在多媒体设备(16)中。 当多媒体设备(16)完成先前发出的命令时,多媒体设备接口(18)将命令从便携式电子设备(10)排队到多媒体设备(16)。

    Color Selection and Chart Styles
    14.
    发明申请
    Color Selection and Chart Styles 审中-公开
    颜色选择和图表样式

    公开(公告)号:US20130093782A1

    公开(公告)日:2013-04-18

    申请号:US13272385

    申请日:2011-10-13

    CPC classification number: G06T11/001 G06T11/206 G09G5/02

    Abstract: Color selection may be provided. First, a selection of a target object may be received and a color selection mode may be entered. Then a color preview may be provided in response to entering the color selection mode. Next, a color selection may be received in response to providing the color preview. A color of a property of the selected target object may then be set to the received color selection.

    Abstract translation: 可以提供颜色选择。 首先,可以接收目标对象的选择,并且可以输入颜色选择模式。 然后可以响应于进入颜色选择模式而提供彩色预览。 接下来,可以响应于提供颜色预览而接收颜色选择。 然后可以将所选择的对象的属性的颜色设置为所接收的颜色选择。

    Mass spectrometic quantification of chemical mixture components
    19.
    发明申请
    Mass spectrometic quantification of chemical mixture components 有权
    化学混合物组分的质谱定量

    公开(公告)号:US20050116159A1

    公开(公告)日:2005-06-02

    申请号:US11023234

    申请日:2004-12-27

    CPC classification number: H01J49/0036

    Abstract: Relative quantitative information about components of chemical or biological samples can be obtained from mass spectra by normalizing the spectra to yield peak intensity values that accurately reflect concentrations of the responsible species. A normalization factor is computed from peak intensities of those inherent components whose concentration remains constant across a series of samples. Relative concentrations of a component occurring in different samples can be estimated from the normalized peak intensities. Unlike conventional methods, internal standards or additional reagents are not required. The methods are particularly useful for differential phenotyping in proteomics and metabolomics research, in which molecules varying in concentration across samples are identified. These identified species may serve as biological markers for disease or response to therapy.

    Abstract translation: 通过对光谱进行归一化,可以从质谱中获得关于化学或生物样品成分的相对定量信息,以产生准确反映负责物种浓度的峰值强度值。 归一化因子是由浓度在一系列样品中保持不变的那些固有成分的峰值强度计算出来的。 发生在不同样品中的组分的相对浓度可以从标准化峰强度估计。 与传统方法不同,不需要内标或附加试剂。 该方法对于蛋白质组学和代谢组学研究中的差异表型特别有用,其中鉴定了样品浓度变化的分子。 这些鉴定的物种可以作为疾病或治疗反应的生物标志物。

Patent Agency Ranking