The present disclosure provides natural gas and petrochemical processing systems including oxidative coupling of methane reactor systems that integrate process inputs and outputs to cooperatively utilize different inputs and outputs of the various systems in the production of higher hydrocarbons from natural gas and other hydrocarbon feedstocks.

The present disclosure provides natural gas and petrochemical processing systems including oxidative coupling of methane reactor systems that integrate process inputs and outputs to cooperatively utilize different inputs and outputs of the various systems in the production of higher hydrocarbons from natural gas and other hydrocarbon feedstocks.

The present invention describes a method to produce high purity hydrocarbon materials from renewable sources. The produced materials are chemically indistinguishable from highly refined mineral oils and/or synthetic hydrocarbons. These renewable hydrocarbon materials can be used as a drop-in replacement for mineral and synthetic hydrocarbon base oils, process fluids, white oils in products such as lubricants, rubber, personal care, pharma.

The present invention describes a method to produce high purity hydrocarbon materials from renewable sources. The produced materials are chemically indistinguishable from highly refined mineral oils and/or synthetic hydrocarbons. These renewable hydrocarbon materials can be used as a drop-in replacement for mineral and synthetic hydrocarbon base oils, process fluids, white oils in products such as lubricants, rubber, personal care, pharma.

Disclosed herein are processes for the production of hydrocarbon fuel products from C2-5 alkanes. Methane is converted to ethylene in a methane thermal olefination reactor operating at a temperature of at least 900 C. and a pressure of at least 150 psig, and without a dehydrogenation catalyst or steam. C2-5 alkanes are converted to olefins in a C2-5 thermal olefination reactor operating at a temperature, pressure and space velocity to convert at least 80% of the alkanes to C2-5 olefins. The ethylene and C2-5 olefins are passed through an oligomerization reactor containing a zeolite catalyst and operating at a temperature, pressure and space velocity to crack, oligomerize and cyclize the olefins. In one aspect, methane in the effluent of the oligomerization reactor is recycled through the C2-5 thermal olefination reactor. Methods for the thermal olefination of methane are also disclosed.

Disclosed is a process for the purification of an organic composition (OC1) by adsorption using an assembly containing at least two adsorbers. The organic composition (OC1) comprising at least one alkane, at least one olefin and at least one compound containing oxygen and/or sulphur is fed into a first adsorber (A1) of the assembly in order to obtain an organic composition (OC2) comprising at least one alkane, at least one olefin and a reduced amount of at least one compound containing oxygen and/or sulphur compared to the respective amount in organic composition (OC1). Hydrogenation of the organic composition (OC2) provides a stream (S2) comprising at least one alkane and a reduced amount of at least one olefin compared to the respective amount in organic composition (OC2) obtained after feeding into the first adsorber (A1). A second adsorber (A2) of the assembly is regenerated by contact with stream (S2).

Disclosed is a process for the purification of an organic composition (OC1) by adsorption using an assembly containing at least two adsorbers. The organic composition (OC1) comprising at least one alkane, at least one olefin and at least one compound containing oxygen and/or sulphur is fed into a first adsorber (A1) of the assembly in order to obtain an organic composition (OC2) comprising at least one alkane, at least one olefin and a reduced amount of at least one compound containing oxygen and/or sulphur compared to the respective amount in organic composition (OC1). Hydrogenation of the organic composition (OC2) provides a stream (S2) comprising at least one alkane and a reduced amount of at least one olefin compared to the respective amount in organic composition (OC2) obtained after feeding into the first adsorber (A1). A second adsorber (A2) of the assembly is regenerated by contact with stream (S2).

The present disclosure provides base stocks and or diesel fuel, and processes for producing such base stocks and or diesel fuel by polymerizing alpha-olefins and internal olefins. The present disclosure further provides polyolefin products useful as base stocks and or diesel fuel. In at least one embodiment, a process includes: i) introducing, neat or in the presence of a solvent, a feed comprising a branched C.sub.5-C.sub.30 internal olefin, with a catalyst compound comprising a group 8, 9, 10, or 11 transition metal and at least one heteroatom and ii) obtaining a C.sub.6-C.sub.100 polyolefin product having one olefin, a methylene content of from about 1 wt % to about 98 wt %, and or a methyl content of from about 1 wt % to about 75 wt %. The feed may further include a linear C.sub.4-C.sub.30 internal olefin, a C.sub.2-C.sub.30 alpha-olefin, or a mixture thereof.

A novel process/system for flexibly producing chemicals and fuels from a petroleum feed such as crude comprise a flashing drum, a first cracker (e.g., a fluidized bed pyrolysis cracker or an oxidative cracker), and an olefin-to-gasoline reaction zone. The process/system can also include a steam cracker and a hydrotreater. The process/system can convert crude oil into hydrogen, C2-C4 olefins, gas oil and distillates with various amounts by adjusting the cut point of the bottoms effluent exiting the flashing drum.

The present disclosure relates generally to processes and systems for producing liquid transportation fuels by converting a feed stream that comprises both isopentane and n-pentane, and optionally, some C6+ hydrocarbons. Isopentane and smaller hydrocarbons are separated to form a first fraction while n-pentane and larger components of the feed stock form a second fraction. Each fraction is then catalytically-activated in a separate reaction zone with a separate catalyst, where the conditions maintained in each zone maximize the conversion of each fraction to olefins and aromatics, while minimizing the production of C1-C4 light paraffins. In certain embodiments, the first fraction is activated at a lower temperature than the second fraction. Certain embodiments additionally comprise mixing at least a portion of the two effluents and contacting with an oligomerization catalyst to provide enhanced yields of aliphatic hydrocarbons that possess the characteristics of a blend component of a liquid transportation fuel or other value-added chemical products.