System and method for producing olefins are disclosed. The method includes using a radial flow moving bed reactor system to catalytically crack paraffins, in multiple stages with continuous catalyst regeneration, to form olefins. The system includes inter-stage heaters to facilitate increase in yield of olefins.

A process (10) for the recovery of hydrocarbons from a Fischer-Tropsch tail gas includes providing a hydrocarbon rich Fischer-Tropsch tail gas (30) which includes hydrocarbons and carbon dioxide, compressing (14) the hydrocarbon rich Fischer-Tropsch tail gas (30) to provide a compressed hydrocarbon rich Fischer-Tropsch tail gas (36, 54), and contacting the compressed hydrocarbon rich Fischer-Tropsch tail gas (36, 54) with a lean oil (64, 54) to recover the hydrocarbons from the compressed hydrocarbon rich Fischer-Tropsch tail gas (36, 54) and to produce a hydrocarbon rich oil (66). Carbon dioxide is stripped (20) from the hydrocarbon rich oil (66) at a pressure which is below the pressure at which the hydrocarbon rich Fischer-Tropsch tail gas (36, 54) is contacted with the lean oil (64, 54), to provide a stripped hydrocarbon oil product (86).

Systems and methods for processing full range naphtha to produce light olefins are disclosed. The systems and methods include separating the full range naphtha into a light naphtha stream and a heavy naphtha stream and integrating a catalytic cracking with a naphtha reforming to process the light naphtha and heavy naphtha streams.

A process for facile separation of lighter hydrocarbon fractions from the heavier fractions of hydrocarbon oil feedstocks is disclosed, which utilizes novel sparging and reverse distillation techniques. The present invention can be utilized for the facile “topping” of crude oil extracted on-site. Moreover, while heavier hydrocarbon fractions may be shipped to refineries for further processing, this invention will also prove useful for quick separation of light fractions produced by cracking processes off-site.

Methods and systems are provided herein utilizing a membrane cascade to separate a hydrocarbon feed into boiling point fractions. Also provided herein are methods for selecting membranes for said cascades to achieve the desired boiling point fraction separation.

A process for treatment of PFO from a steam cracking zone includes selectively hydrogenating PFO or a portion thereof for conversion of polyaromatics compounds contained in the PFO into aromatic compounds with one benzene ring to produce a selectively hydrogenated stream. The selectively hydrogenated stream is selectively hydrocracked for selective ring opening and dealkylation to produce a selectively hydrocracked BTX+ stream. The selectively hydrocracked BTX+ stream is separated into BTX compounds. Optionally the PFO is separated into a first stream containing C9+ aromatics compounds with one benzene ring, and a second stream containing C10+ aromatic compounds, whereby the first stream containing C9+ aromatics compounds with one benzene ring is passed to the selective hydrocracking step, and the feed to the selective hydrogenation step comprises all or a portion of the second stream containing C10+ aromatic compounds.

The present invention relates to a device and to a process for the fluidized bed catalytic cracking of a hydrocarbon feedstock, in which: a first feedstock (2) is cracked in a dense fluidized bed reactor (1) in the presence of a catalyst (3) to produce a first effluent; and at least one second feedstock (10) is cracked in a transport fluidized bed reactor (4) in the presence of the catalyst (3) supplied by the dense fluidized bed reactor (1) to produce a second effluent, the second feedstock (10) being a heavier feedstock than the first feedstock (2).

The present invention relates to a process and system for complete conversion of crude oils by integrating Desalter unit, Atmospheric and vacuum column, high severity FCC process, Naphtha cracking process, residue slurry hydrocracking process, Delayed coking process, Selective mild hydrocracking aromatic production unit, Dehydrogenation units, Aromatic/olefin recovery section, gasifier unit along with syngas to olefins conversion section.

Compositions can include mixtures having from about 2 wt % to about 40 wt % of C.sub.10-C.sub.20 linear paraffins based on the weight of the mixture, from about 60 wt % to about 98 wt % of C.sub.10-C.sub.20 branched saturated hydrocarbons based on the weight of the mixture, and less than or equal to about 30 wt % of C.sub.20+ saturated hydrocarbons based on the weight of the mixture. Methods to obtain these compositions can include the isomerization of one or more C.sub.10-C.sub.20 alpha olefins under skeletal isomerization conditions to obtain an isomerization mixture and the hydrotreating of the isomerization mixture.

A system for producing a hydrocarbon by high-temperature Fischer-Tropsch synthesis is described. The system includes a Fischer-Tropsch synthesis unit, a reaction water separation unit, and a catalyst reduction unit. The catalyst reduction unit uses a gas containing the tail gas of the synthesis unit as a reducing gas and a small amount of synthesis gas for adjusting the hydrogen to carbon ratio, to react with the Fischer-Tropsch synthesis catalyst. After the reduction reaction, the reacted gas is cooled to room temperature, and enters a gas-liquid separator to obtain a gas phase and a liquid phase. The gas phase flows to a cryogenic separation unit to recover gaseous hydrocarbons. The liquid phase is separated into reaction water and Fischer-Tropsch oil products. The reduced catalyst is sent to the Fischer-Tropsch synthesis unit. The catalyst reduction unit achieves high energy efficiency, product diversity, and risk resistance.