Electrically heated autoclave apparatus
    22.
    发明授权
    Electrically heated autoclave apparatus 失效
    电加热自动装置

    公开(公告)号:US3609296A

    公开(公告)日:1971-09-28

    申请号:US3609296D

    申请日:1970-03-27

    Inventor: BLAIR JOE B

    CPC classification number: B01J3/044 F24H1/102 F27D11/02 Y10S165/902

    Abstract: An autoclave apparatus comprising an autoclave forming a product-receiving chamber having an inlet port in one end and an outlet port in the opposite end and being, further, formed with an access opening. An electrically heated heat exchanger is formed with a chamber which contains heat storage means and such chamber has an inlet in one end and an outlet in the opposite end. Conduits connect the inlet to the autoclave with the outlet from the heat exchanger and the outlet of the autoclave with the inlet to the heat exchanger. Means is provided for supplying gas to the system whereby such system may be pressurized with the gas and such gas circulated through the autoclave and in heatexchange relationship with the heat storage means to heat such gas to an elevated temperature thereby providing an atmosphere in the product-receiving chamber of the desired temperature and pressure.

    POLYMERISATION REACTOR
    24.
    发明申请
    POLYMERISATION REACTOR 有权
    聚合反应器

    公开(公告)号:US20110002816A1

    公开(公告)日:2011-01-06

    申请号:US12735349

    申请日:2009-02-04

    Abstract: A tubular reactor for use in polymerisation reactions is described, having a design pressure PR of 40-65 barg, at least a portion of which is oriented vertically and at least part of which vertical portion is surrounded by a concentric jacket for the passage of cooling fluid, wherein the design pressure in barg of the jacket PJ is less than 0.0018.PR2.25. Another aspect of the invention concerns a tubular reactor for use in polymerisation reactions having a design pressure PR of 40-65 barg, at least a portion of which is oriented vertically and at least part of which vertical portion is surrounded by a concentric jacket for the passage of cooling fluid, wherein the actual thickness of the reactor wall is either no more than 2 mm greater and/or no more than 10% greater than the minimum wall thickness required to withstand the design pressure PR as calculated according to the ASME Boiler and Pressure Vessel code.

    Abstract translation: 描述了用于聚合反应的管式反应器,其设计压力PR为40-65巴,其至少一部分垂直取向,并且其至少一部分垂直部分被同心夹套围绕以便冷却通过 流体,其中护套PJ的设计压力barg小于0.0018.PR2.25。 本发明的另一方面涉及一种用于聚合反应的管式反应器,其设计压力PR为40-65巴,其设计压力PR至少为40-65巴,其至少一部分垂直取向,并且其至少部分垂直部分被同心夹套围绕,用于 冷却流体的通过,其中反应器壁的实际厚度不得比承受根据ASME锅炉计算的设计压力PR所需的最小壁厚大不超过2mm和/或不超过10%,以及 压力容器代码。

    Method and apparatus for producing hydrogen peroxide from hydrogen and oxygen
    25.
    发明申请
    Method and apparatus for producing hydrogen peroxide from hydrogen and oxygen 失效
    从氢气和氧气生产过氧化氢的方法和装置

    公开(公告)号:US20030161783A1

    公开(公告)日:2003-08-28

    申请号:US10326286

    申请日:2002-12-23

    Abstract: The invention relates to a method and apparatus for safely producing hydrogen peroxide by injecting dispersed minute bubbles of hydrogen and oxygen into a rapidly flowing liquid medium. The minute bubbles are surrounded by the liquid medium of sufficient volume for preventing an explosive reaction between the hydrogen and oxygen. The liquid medium is formed of an acidic aqueous solution and a Group VIII metal catalyst. Hydrogen is sparged into the flowing medium for dissolution of the hydrogen in the medium. Oxygen bubbles are reacted with the dissolved hydrogen for producing hydrogen peroxide. Preferably, the liquid medium has a velocity of at least 10 feet per second for providing a bubbly flow regime in the reactor. The invention allows the direct combination of oxygen and hydrogen while preventing propagation of an explosive condition within the reactor. The method and apparatus provide for the safe production of hydrogen peroxide with low manufacturing costs.

    Abstract translation: 本发明涉及通过将分散的氢气和氧气的微小气泡注入到快速流动的液体介质中来安全地生产过氧化氢的方法和装置。 微小气泡被足够体积的液体介质包围,以防止氢气和氧气之间的爆炸性反应。 液体介质由酸性水溶液和VIII族金属催化剂形成。 将氢气喷射到流动介质中,以将氢溶解在介质中。 氧气与溶解的氢气反应生成过氧化氢。 优选地,液体介质具有至少10英尺/秒的速度,以在反应器中提供气泡流动状态。 本发明允许氧和氢的直接组合,同时防止反应器内的爆炸性条件的扩散。 该方法和装置以低制造成本提供安全生产过氧化氢。

    PYROLYTIC REACTOR AND METHOD OF USING
    29.
    发明申请
    PYROLYTIC REACTOR AND METHOD OF USING 审中-公开
    热解反应器及其使用方法

    公开(公告)号:WO2016209648A1

    公开(公告)日:2016-12-29

    申请号:PCT/US2016/037145

    申请日:2016-06-13

    Applicant: UOP LLC

    CPC classification number: B01J6/008 B01J3/044 C07C2/78 C07C11/24

    Abstract: Methods and apparatus to produce alkynes are described. The method includes combusting fuel and an oxidizer in a combustion zone to create a carrier gas stream, which is accelerated to supersonic speed in an expansion zone. A feedstock material is injected into a feedstock injection zone using two or more pluralities of injection nozzles. The injection nozzles are arranged annularly. The carrier gas stream is transitioned from supersonic speed to subsonic speed to create a shockwave in a reaction zone. The reaction zone is directly connected to the feedstock injection zone, and the shockwave is created adjacent to the feedstock injection zone. The carrier gas stream and the feedstock material are simultaneously mixed and reacted.

    Abstract translation: 描述了产生炔烃的方法和装置。 该方法包括在燃烧区燃烧燃料和氧化剂以产生载气流,其在膨胀区中被加速到超音速。 使用两个或多个多个注射喷嘴将原料注入原料注入区。 注射喷嘴环状布置。 载气流从超音速转变为亚音速,在反应区产生冲击波。 反应区直接连接到原料注入区,并且在原料注入区附近产生冲击波。 载气流和原料同时混合并反应。

    METHOD AND APPARATUS FOR CONDUCTING CHEMICAL REACTIONS AT SUPERCRITICAL CONDITIONS
    30.
    发明申请
    METHOD AND APPARATUS FOR CONDUCTING CHEMICAL REACTIONS AT SUPERCRITICAL CONDITIONS 审中-公开
    用于在超临界条件下进行化学反应的方法和装置

    公开(公告)号:WO1988007890A1

    公开(公告)日:1988-10-20

    申请号:PCT/US1988000979

    申请日:1988-03-31

    CPC classification number: B01J3/008 B01J3/044 Y02P20/544

    Abstract: A continuously flowing fluid is processed by being fed to the top of a hydraulic downdraft column (17) which is of a height such that the pressure at the bottom thereof will approximately be at the pressure necessary to create supercritical water conditions. The fluid is conducted to the bottom of the column (17) and received in a reaction chamber (21) in which the majority of the fluid is recirculated around an annular baffle plate (24). The material in the reaction chamber (21) is heated to a temperature above that necessary to create supercritical water conditions by an independent reaction taking place in a heating chamber (32). The result is that the fluid will undergo chemical reactions at the supercritical temperature and pressure range and will be of a lower specific gravity than the unprocessed fluid. The material not being recirculated in the chamber (21) is fed to one of two updraft columns (30, 31), a start-up column (30) used to preheat the material in the downdraft column (17) during initiation of the process, and a second column (31) isolated from the downdraft column (17) so as not to transmit any heat thereto during normal operation of the process. The temperature of the fluid in the downdraft column (17) is thereby controlled to prevent decomposition of the material until the fluid enters the reaction chamber (21) at which time it is abruptly brought up to the supercritical water temperature.

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