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.

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.

A polymerization process may include: polymerizing a monomer having 4 or less carbons and a comonomer having 6 or more carbons in the presence of an inert isomer/saturate of the comonomer to yield a product stream comprising a polymer, unreacted monomer, unreacted comonomer, and the inert isomer/saturate of the comonomer; separating the product stream into (a) a polymer stream and (b) an unreacted components stream; and separating the unreacted components stream in a distillation column into (a) an overhead stream comprising the unreacted monomer and (b) a bottoms stream comprising the comonomer and the inert isomer/saturate of the comonomer, wherein a concentration of C5 hydrocarbons in the overhead stream is higher than a concentration of the C5 hydrocarbons in the unreacted components stream, and wherein a concentration of C6+ hydrocarbons in the bottoms stream is higher than a concentration of the C6+ hydrocarbons in the unreacted components stream.

A polymerization process may include: polymerizing a monomer having 4 or less carbons and a comonomer having 6 or more carbons in the presence of an inert isomer/saturate of the comonomer to yield a product stream comprising a polymer, unreacted monomer, unreacted comonomer, and the inert isomer/saturate of the comonomer; separating the product stream into (a) a polymer stream and (b) an unreacted components stream; and separating the unreacted components stream in a distillation column into (a) an overhead stream comprising the unreacted monomer and (b) a bottoms stream comprising the comonomer and the inert isomer/saturate of the comonomer, wherein a concentration of C5 hydrocarbons in the overhead stream is higher than a concentration of the C5 hydrocarbons in the unreacted components stream, and wherein a concentration of C6+ hydrocarbons in the bottoms stream is higher than a concentration of the C6+ hydrocarbons in the unreacted components stream.

Processes to selectively crack alkyne compounds from a hydrocarbon stream including olefinic and di-olefinic compounds are described. The process includes contacting the hydrocarbon stream with a supported CuO catalyst under conditions sufficient to crack the alkynes to form a product stream that included cracked compounds and further separating the cracked organic compounds from the hydrocarbon stream.

Processes to selectively crack alkyne compounds from a hydrocarbon stream including olefinic and di-olefinic compounds are described. The process includes contacting the hydrocarbon stream with a supported CuO catalyst under conditions sufficient to crack the alkynes to form a product stream that included cracked compounds and further separating the cracked organic compounds from the hydrocarbon stream.

A supported catalyst, its method of preparation and use in hydrogenation methods, which catalyst contains an oxide substrate that is for the most part calcined aluminum and an active phase that contains nickel, with the nickel content between 5 and 65% by weight in relation to the total mass of the catalyst, with the active phase not containing a metal from group VIB, the nickel particles having a diameter that is less than or equal to 20 nm, the catalyst having a median mesopore diameter of between 14 nm and 30 nm, a median macropore diameter of between 50 and 200 nm, a mesopore volume that is measured by mercury porosimetry that is greater than or equal to 0.40 mL/g, and a total pore volume that is measured by mercury porosimetry that is greater than or equal to 0.42 mL/g.

A supported catalyst, its method of preparation and use in hydrogenation methods, which catalyst contains an oxide substrate that is for the most part calcined aluminum and an active phase that contains nickel, with the nickel content between 5 and 65% by weight in relation to the total mass of the catalyst, with the active phase not containing a metal from group VIB, the nickel particles having a diameter that is less than or equal to 20 nm, the catalyst having a median mesopore diameter of between 14 nm and 30 nm, a median macropore diameter of between 50 and 200 nm, a mesopore volume that is measured by mercury porosimetry that is greater than or equal to 0.40 mL/g, and a total pore volume that is measured by mercury porosimetry that is greater than or equal to 0.42 mL/g.

Disclosed herein are processes for producing neopentane. The processes generally relate to demethylating diisobutylene to produce neopentane. The diisobutylene may be provided by the dimerization of isobutylene.

Disclosed herein are processes for producing neopentane. The processes generally relate to demethylating diisobutylene to produce neopentane. The diisobutylene may be provided by the dimerization of isobutylene.