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    • 2. 发明授权
    • Freeze-wash method for separating carbon dioxide and ethane
    • 用于分离二氧化碳和乙烷的冷冻洗涤方法
    • US4246015A
    • 1981-01-20
    • US109012
    • 1979-12-31
    • Ralph E. Styring, Jr.
    • Ralph E. Styring, Jr.
    • C07C7/14F25J3/02
    • F25J3/0238C07C7/14F25J3/0209F25J3/0266F25J2205/20F25J2205/30F25J2210/62Y02C10/12Y02P20/152Y10S62/929
    • A method is disclosed for separating a mixture of carbon dioxide and ethane derived from a prior separation stage. The separation is accomplished by freezing the carbon dioxide in an azeotrope of carbon dioxide and ethane and washing the ethane from the solid carbon dioxide with a liquid hydrocarbon having at least three carbon atoms. The freezing stage may be preceded by distillation of a carbon dioxide-ethane mixture to form the azeotrope. The carbon dioxide and wash hydrocarbon may be separated in a subsequent distillation stage. In addition, if desired, the ethane-wash hydrocarbon mixture may be similarly separated in a subsequent distillation stage. The method is useful in carbon dioxide separation facilities where it is desirable to recover ethane that would otherwise be lost.
    • 公开了一种用于分离来自先前分离级的二氧化碳和乙烷的混合物的方法。 通过将二氧化碳冷冻在二氧化碳和乙烷的共沸物中并用具有至少三个碳原子的液态烃从固体二氧化碳洗涤乙烷来实现分离。 之前可以通过蒸馏二氧化碳 - 乙烷混合物来形成共沸物。 二氧化碳和洗涤烃可以在随后的蒸馏阶段中分离。 此外,如果需要,乙烷 - 洗涤烃混合物可以在随后的蒸馏阶段中类似地分离。 该方法在二氧化碳分离设备中是有用的,其中希望回收否则将丢失的乙烷。
    • 3. 发明授权
    • Two stage carbon dioxide and methane separation
    • 二级二氧化碳和甲烷分离
    • US4351655A
    • 1982-09-28
    • US256197
    • 1981-04-21
    • Ralph E. Styring, Jr.
    • Ralph E. Styring, Jr.
    • F25J3/02
    • F25J3/0266F25J3/0209F25J3/0233F25J3/0238F25J2215/62Y02C10/12Y10S62/929
    • A method is disclosed for standard distillation of a mixture of carbon dioxide and ethane derived from a prior separation state in a way that greater than normal separation is obtained. The greater separation is accomplished in two stages. In the first stage, an azeotrope of carbon dioxide and ethane is formed in a first distillation column at a first pressure. The azeotropic mixture is then transferred to a second distillation column operated at a second pressure. The second pressure is at least 150 psia greater or less than the first pressure and is sufficient to shift the phase curves or equilibrium ratios so that additional separation of the ethane and carbon dioxide is accomplished in the second column. Preferably, if the concentration of carbon dioxide in the original ethane-carbon dioxide mixture is less than the concentration of carbon dioxide in the azeotrope, the pressure in the second column will be lower than pressure in the first column. The reverse is preferred when the concentration of carbon dioxide in the original mixture is greater than the concentration of carbon dioxide in the azeotrope. The method is useful in carbon dioxide separation facilities where it is desirable to recover additional ethane that would otherwise be lost.
    • 公开了一种用于以大于正常分离获得的方式对来自先前分离状态的二氧化碳和乙烷的混合物进行标准蒸馏的方法。 更大的分离在两个阶段完成。 在第一阶段,在第一压力下在第一蒸馏塔中形成二氧化碳和乙烷的共沸物。 然后将共沸混合物转移到在第二压力下操作的第二蒸馏塔。 第二压力比第一压力大至少150psia,并且足以使相曲线或平衡比移动,使得在第二塔中实现乙烷和二氧化碳的额外分离。 优选地,如果原始乙烷 - 二氧化碳混合物中二氧化碳的浓度小于共沸物中二氧化碳的浓度,则第二塔中的压力将低于第一塔中的压力。 当原始混合物中二氧化碳的浓度大于共沸物中二氧化碳的浓度时,反之亦然。 该方法在二氧化碳分离设备中是有用的,其中希望回收否则将丢失的另外的乙烷。
    • 4. 发明授权
    • Separating spent mineral matter from heat carriers
    • 将废弃的矿物质与热载体分开
    • US4314899A
    • 1982-02-09
    • US220006
    • 1980-12-23
    • Ralph E. Styring, Jr.
    • Ralph E. Styring, Jr.
    • B07B4/02B07B7/01B07B11/06C10G1/02B07B9/02
    • B07B7/01B07B11/06B07B4/02C10G1/02
    • In the pyrolysis of crushed mined hydrocarbonaceous mineral solids with hot heat carrying solids, the heat carrying solids are recovered from the pyrolyzed mineral matter, heated and recycled back to a primary pyrolysis zone. At an appropriate point in the process, a mixture of heat carriers and pyrolyzed mineral matter is fed into a chamber through which an elutriating gas is flowed. Prior to entry into the chamber, the mixture is separated into two streams having different relative concentrations of spent mineral matter. The stream with the least amount of spent mineral matter is fed into the chamber at a point below the point where the stream with the larger amount of spent mineral matter is fed. This prevents surging of the elutriation system.
    • 在具有热载热固体的破碎的开采的含烃矿物固体的热解中,热交换固体从热解的矿物质中回收,加热并再循环回初级热解区。 在该过程中的适当点,将热载体和热解的矿物质的混合物进料到经过淘洗气体流过的室中。 在进入室之前,将混合物分离成具有不同相对浓度的废矿物质的两股流。 将具有最少量的废矿物质的料流在低于具有较大量的废矿物质的料流进料点的点处进料到室中。 这样可以防止淘汰淘汰系统的冲击。
    • 5. 发明授权
    • Retorting hydrocarbonaceous solids
    • 蒸馏含烃固体
    • US4218304A
    • 1980-08-19
    • US973834
    • 1978-12-28
    • Ralph E. Styring, Jr.
    • Ralph E. Styring, Jr.
    • C10B49/02C10G1/02C10G1/00
    • C10G1/02C10B49/02
    • Mined, crushed hydrocarbonaceous solids are pyrolyzed in a retort with a gas containing hydrocarbons. The gas is heated to a suitable temperature of at least 600.degree. F. Thereafter, a relatively small amount of oxygen is added to the heated gas outside the retort. The resulting mixture is then flowed into the retort. The amount of oxygen is theoretically sufficient to raise the temperature of the heated gas at least 100.degree. F., but is less than the amount theoretically sufficient to react with all of the hydrocarbons in the heated gas. The process is applicable to any type of retort wherein a retort recycle gas containing hydrocarbons is heated outside the retort and is then injected into the retort to provide a source of heat for pyrolyzing hydrocarbonaceous solids in the retort. The advantages of this modified indirect heated retorting method depends on the type of retort. This method provides added control over carbonate decomposition, coking or carbonization of the gas during heating, total gas flow, process variations, and the heat requirements and thermal efficiency of the process.
    • 粉碎的含烃固体在含有烃的气体的蒸馏器中热解。 将气体加热到至少600°F的合适温度。此后,将较少量的氧气加入到蒸馏器外部的加热气体中。 然后将所得混合物流入蒸馏器。 在理论上,氧气的量足以将加热气体的温度升高至少100°F,但小于理论上足以与加热气体中的所有烃反应的量。 该方法适用于任何类型的蒸馏器,其中将含有烃的蒸馏回收气体加热到蒸馏器外部,然后将其注入蒸馏器中以提供用于在蒸馏器中热解烃类固体的热源。 这种改进的间接加热蒸煮方法的优点取决于蒸馏器的类型。 该方法对加热过程中的碳酸盐分解,焦化或碳化,总气体流动,工艺变化以及过程的热需求和热效率提供了附加控制。