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    • 21. 发明授权
    • Biased degasser for fluidized bed outlet
    • 用于流化床出口的偏置脱气机
    • US4289729A
    • 1981-09-15
    • US61117
    • 1979-07-26
    • George D. MyersPaul W. Walters
    • George D. MyersPaul W. Walters
    • C10G11/18B01J4/00B01J8/00B01J8/24F27B15/08B01J8/28F26B17/10
    • B01J8/005B01J8/1872
    • A degaser is disclosed for an outlet conduit into which solids are transferred from a fluidized bed within a larger vessel and comprises a curvilinear wall extending upward from the upper end of the outlet conduit and beveled at an angle to the vertical to form an outlet with a rim having a high side and a low side. The degaser is positioned with its high side far below the solids inlet into the vessel and its low side near the bottom of the fluidized bed. The biased rim may take various shapes and the degaser wall may extend only partially around the upper conduit end. Fluidizing gas can be introduced into the bed either above or below the low side of the degaser. The degaser may also include a baffle arranged within the vessel in cooperative relation to the rim.
    • 公开了一种用于出口导管的脱墨机,固体从较大容器中的流化床转移到其中,并且包括从出口导管的上端向上延伸并与垂直方向成一定角度的曲线壁,形成具有 边缘具有高边和低边。 排气机的高侧定位成远离固体入口进入容器,其低侧靠近流化床的底部。 偏置的轮辋可以采取各种形状,并且致动器壁可仅部分地围绕上管道端部延伸。 流化气体可以在除气剂的低侧上方或下方引入床中。 除气剂还可以包括与容器内的配合关系的挡板。
    • 22. 发明授权
    • Carbo-metallic oil conversion
    • 碳转移金属油
    • US4708785A
    • 1987-11-24
    • US694719
    • 1985-03-20
    • George D. Myers, deceased
    • George D. Myers, deceased
    • B01J29/06B01J29/90C10G11/05C10G11/18
    • C10G11/05B01J29/06B01J29/90C10G11/18Y02P30/446
    • Heat balance in a residual oil conversion unit can be controlled as a function of Conradson carbon of the feed, water added to the feed, hydrogen in the coke produced, CO.sub.2 /CO ratio, etc. Preferably, riser outlet temperature can be controlled to less than about 538.degree. C. (1000.degree. F.) at CO.sub.2 /CO flue gas ratios of 3/1 or less. Especially preferred are operations in a two-stage regenerator with cracking catalyst comprising at least 5000 ppm of Ni+V and residual carbon on regenerated catalyst of at least 0.1 wt. %. The contact time in the second stage of the regenerator being less than about 1/2 of that employed in the first stage, and with oxygen-lean gas being employed in the first stage. The heat transferred by the catalyst to the residual oil feed is preferably limited to about 500 to 1200 btu per pound of oil feed.
    • 剩余油转化单元中的热平衡可以作为进料的康拉德森碳,加入进料中的水,生产的焦炭中的氢,CO 2 / CO比等进行控制。优选地,提升管出口温度可以控制到更低 大于538℃(1000°F),CO2 / CO烟气比为3/1以下。 特别优选的是在具有至少5000ppm的Ni + V的裂化催化剂和再生催化剂上的残余碳至少为0.1wt。%的两级再生器中的操作。 %。 再生器的第二阶段的接触时间小于第一阶段中使用的接触时间的约1/2,而在第一阶段使用贫氧气体。 由催化剂转移到残油进料的热量优选限制在每磅油进料约500至1200btu。
    • 23. 发明授权
    • Carbo-metallic oil conversion
    • 碳转移金属油
    • US4602993A
    • 1986-07-29
    • US485574
    • 1983-04-01
    • George D. Myers
    • George D. Myers
    • C10G11/05C10G11/18
    • C10G11/05C10G11/18
    • A process is disclosed for the production of high octane gasoline and/or other valuable lower molecular weight products from carbo-metallic oils. Examples include crude oil, topped crude, reduced crude, residua, the extract from solvent de-asphalting and other heavy hydrocarbon fractions. These carbo-metallic oils contain quantities of coke precursors and heavy metal catalyst poisons substantially in excess of what is normally considered acceptable for FCC processing (fluid catalytic cracking) and substantial amounts of sulfur, nitrogen and other troublesome components may also be present. Such carbo-metallic oils are converted to the desired products in a catalytic conversion process. Named "RCC" (Reduced Crude Conversion) after a particularly common or useful carbo-metallic feed, the present process is by no means restricted to reduced crude or to oils of petroleum origin, having utility in the processing of oils from coal, shale and other sources.
    • PCT No.PCT / US82 / 00675 Sec。 371日期:1983年4月1日 102(e)日期1983年4月1日PCT提交1982年5月13日PCT公布。 出版物WO83 / 04042 日期为1983年11月24日。公开了用于从碳 - 金属油生产高辛烷值汽油和/或其它有价值的低分子量产品的方法。 实例包括原油,顶部粗品,还原原油,残渣,来自溶剂脱沥青的提取物和其它重质烃馏分。 这些碳金属油含有大量的焦炭前体和重金属催化剂毒素,其基本上超过通常被认为可接受的FCC处理(流化催化裂化),并且还可能存在大量的硫,氮和其它麻烦的组分。 这种碳金属油在催化转化过程中转化为所需产物。 在特别常见或有用的碳金属饲料之后,被命名为“RCC”(减少原油转化),本方法绝不限于将原油或石油来源的油减少,可用于加工来自煤,页岩和 其他来源。
    • 24. 发明授权
    • Addition of MgCl.sub.2 to catalyst for cracking carbo-metallic feed oils
    • US4376696A
    • 1983-03-15
    • US246751
    • 1981-03-23
    • George D. Myers, deceased
    • George D. Myers, deceased
    • B01J27/138B01J27/00B01J27/10B01J29/00B01J29/06B01J29/90B01J38/30C10G11/00C10G11/02C10G11/18C10G11/05C10G11/08
    • B01J29/06B01J29/90C10G11/18Y02P30/446
    • A process for economically converting carbo-metallic oils to lighter products while adding magnesium chloride to modify heat output. The carbo-metallic oils contain 650.degree. F. and material which is characterized by a carbon residue on pyrolysis of at least about 1 and a Nickel Equivalents of heavy metals content of at least about 4 parts per million. This process comprises flowing the carbo-metallic oil together with particulate cracking catalyst through a progressive flow type reactor having an elongated reaction chamber, which is at least in part vertical or inclined, for a predetermined vapor riser residence time in the range of about 0.5 to about 10 seconds, at a temperature of about 900.degree. to about 1400.degree. F., and under a pressure of about 10 to about 50 pounds per square inch absolute sufficient for causing a conversion per pass in the range of about 50% to about 90% while producing coke in amounts in the range of about 6 to about 14% by weight based on fresh feed, and laying down coke on the catalyst in amounts in the range of about 0.3 to about 3% by weight. The spent, coke-laden catalyst from the stream of hydrocarbons formed by vaporized feed and resultant cracking products is separated and regenerated in one or more regeneration beds in one or more regeneration zones by burning the coke on the spent catalyst with oxygen. The bed density is in the range of about 25 to about 50 pounds per cubic foot and the bed or beds are sustained by fluidization gas containing combustion-supporting gas having a linear velocity in the range of about 0.2 to about 4 feet per second. MgCl.sub.2 is added to the catalyst and is converted to MgO, which reduces sulfur oxide emissions, and a chlorine component, which reduces the CO.sub.2 /CO ratio, thereby reducing the heat output of the regenerator. The catalyst particles are retained in the regeneration zone or zones in contact with the combustion-supporting gas for an average total residence time in said zone or zones of about 5 to about 30 minutes to reduce the level of carbon on the catalyst to about 0.25% by weight or less. The regenerated catalyst is recycled to the reactor and contacted with fresh carbon-metallic oil.
    • 25. 发明授权
    • Addition of chlorine to regenerator
    • US4375404A
    • 1983-03-01
    • US246782
    • 1981-03-23
    • George D. Myers, deceased
    • George D. Myers, deceased
    • B01J29/06B01J29/90C10G11/18C10G11/05C10G11/08
    • C10G11/182B01J29/06B01J29/90Y02P30/446
    • A process for economically converting carbo-metallic oils to lighter products. The carbo-metallic oils contain 650.degree. F. and material which is characterized by a carbon residue on pyrolysis of at least about 1 and a Nickel Equivalents of heavy metals content of at least about 4 parts per million. This process comprises flowing the carbo-metallic oil together with particulate cracking catalyst through a progressive flow type reactor having an elongated reaction chamber, which is at least in part vertical or inclined, for a predetermined vapor riser residence time in the range of about 0.5 to about 10 seconds, at a temperature of about 900.degree. to about 1400.degree. F., and under a pressure of about 10 to about 50 pounds per square inch absolute sufficient for causing a conversion per pass in the range of about 50% to about 90% while producing coke in amounts in the range of about 6 to about 14% by weight based on fresh feed, and laying down coke on the catalyst in amounts in the range of about 0.3 to about 3% by weight. The spent, coke-laden catalyst from the stream of hydrocarbons formed by vaporized feed and resultant cracking products is separated and regenerated in one or more regeneration beds in one or more regeneration zones by burning the coke on the spent catalyst with oxygen in the presence of chlorine. The bed density is in the range of about 25 to about 50 pounds per cubic foot and the bed or beds are sustained by fluidization gas containing combustion-supporting gas having a linear velocity in the range of about 0.2 to about 4 feed per second. The chlorine reduces the CO.sub.2 /CO ratio, thereby reducing the heat output of the regenerator. The catalyst particles are retained in the regeneration zone or zones in contact with the combustion-supporting gas for an average total residence time in said zone or zones of about 5 to about 30 minutes to reduce the level of carbon on the catalyst to about 0.25% by weight or less. The regenerated catalyst is recycled to the reactor and contacted with fresh carbo-metallic oil.