Patent classifications
C07C7/11
SEPARATING AROMATIC ISOMERS USING AQUEOUS SOLUTIONS OF CUCURBITURIL MACROCYCLES
The present disclosure provide processes of separating aromatic isomers; liquid-liquid extraction systems and processes; liquid-liquid extraction solvents; cucurbituril macrocycle selective for the extraction of aromatic isomers; related materials, methods, and systems; and the like. The process of separating aromatic isomers may include contacting an isomers solution including one or more aromatic isomers, with an aqueous solution including a cucurbituril macrocycle, to produce a first aqueous phase and a first organic phase, wherein the cucurbituril macrocycle is selective for the extraction of at least one of said aromatic isomers.
SEPARATING AROMATIC ISOMERS USING AQUEOUS SOLUTIONS OF CUCURBITURIL MACROCYCLES
The present disclosure provide processes of separating aromatic isomers; liquid-liquid extraction systems and processes; liquid-liquid extraction solvents; cucurbituril macrocycle selective for the extraction of aromatic isomers; related materials, methods, and systems; and the like. The process of separating aromatic isomers may include contacting an isomers solution including one or more aromatic isomers, with an aqueous solution including a cucurbituril macrocycle, to produce a first aqueous phase and a first organic phase, wherein the cucurbituril macrocycle is selective for the extraction of at least one of said aromatic isomers.
PROCESS FOR PREPARING 1,3-BUTADIENE FROM N-BUTENES BY OXIDATIVE DEHYDROGENATION
The invention relates to a process for preparing butadiene from n-butenes, comprising the steps of: A) providing an input gas stream a comprising n-butenes, B) feeding the input gas stream a comprising n-butenes and a gas containing at least oxygen into at least one oxidative dehydrogenation zone and oxidatively dehydrogenating n-butenes to butadiene, giving a product gas stream b comprising butadiene, unconverted n-butenes, water vapor, oxygen, low-boiling hydrocarbons and high-boiling secondary components, with or without carbon oxides and with or without inert gases; Ca) cooling the product gas stream b by contacting with a cooling medium in at least one cooling zone, the cooling medium being at least partly recycled and having an aqueous phase and an organic phase, Cb) compressing the cooled product gas stream b which may have been depleted of high-boiling secondary components in at least one compression stage, giving at least one aqueous condensate stream c1 and one gas stream c2 comprising butadiene, n-butenes, water vapor, oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases; D) removing uncondensable and low-boiling gas constituents comprising oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases, as gas stream d2 from the gas stream c2 by absorbing the C.sub.4 hydrocarbons comprising butadiene and n-butenes in an absorbent, giving an absorbent stream laden with C.sub.4 hydrocarbons and the gas stream d2, and then desorbing the C.sub.4 hydrocarbons from the laden absorbent stream, giving a C.sub.4 product gas stream d1, E) separating the C.sub.4 product stream d1 by extractive distillation with a butadiene-selective solvent into a stream e1 comprising butadiene and the selective solvent and a stream e2 comprising n-butenes; F) distilling the stream e1 comprising butadiene and the selective solvent into a stream f1 consisting essentially of the selective solvent and a stream f2 comprising butadiene, wherein stage Cb) comprises at least two compression stages Cba) and at least two cooling stages Cbb) configured in the form of quench columns, the cooling in the cooling stages being effected by direct contacting with a biphasic cooling medium having an aqueous phase and an organic phase.
PROCESS FOR PREPARING 1,3-BUTADIENE FROM N-BUTENES BY OXIDATIVE DEHYDROGENATION
The invention relates to a process for preparing butadiene from n-butenes, comprising the steps of: A) providing an input gas stream a comprising n-butenes, B) feeding the input gas stream a comprising n-butenes and a gas containing at least oxygen into at least one oxidative dehydrogenation zone and oxidatively dehydrogenating n-butenes to butadiene, giving a product gas stream b comprising butadiene, unconverted n-butenes, water vapor, oxygen, low-boiling hydrocarbons and high-boiling secondary components, with or without carbon oxides and with or without inert gases; Ca) cooling the product gas stream b by contacting with a cooling medium in at least one cooling zone, the cooling medium being at least partly recycled and having an aqueous phase and an organic phase, Cb) compressing the cooled product gas stream b which may have been depleted of high-boiling secondary components in at least one compression stage, giving at least one aqueous condensate stream c1 and one gas stream c2 comprising butadiene, n-butenes, water vapor, oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases; D) removing uncondensable and low-boiling gas constituents comprising oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases, as gas stream d2 from the gas stream c2 by absorbing the C.sub.4 hydrocarbons comprising butadiene and n-butenes in an absorbent, giving an absorbent stream laden with C.sub.4 hydrocarbons and the gas stream d2, and then desorbing the C.sub.4 hydrocarbons from the laden absorbent stream, giving a C.sub.4 product gas stream d1, E) separating the C.sub.4 product stream d1 by extractive distillation with a butadiene-selective solvent into a stream e1 comprising butadiene and the selective solvent and a stream e2 comprising n-butenes; F) distilling the stream e1 comprising butadiene and the selective solvent into a stream f1 consisting essentially of the selective solvent and a stream f2 comprising butadiene, wherein stage Cb) comprises at least two compression stages Cba) and at least two cooling stages Cbb) configured in the form of quench columns, the cooling in the cooling stages being effected by direct contacting with a biphasic cooling medium having an aqueous phase and an organic phase.
METHOD FOR IMPROVING PROPYLENE RECOVERY FROM FLUID CATALYTIC CRACKER UNIT
The present invention relates to a method for treating a cracked stream stemming from a fluid catalytic cracker unit (FCCU) in order to improve propylene recovery. The present invention also relates to the corresponding installation to implement the method.
METHOD FOR IMPROVING PROPYLENE RECOVERY FROM FLUID CATALYTIC CRACKER UNIT
The present invention relates to a method for treating a cracked stream stemming from a fluid catalytic cracker unit (FCCU) in order to improve propylene recovery. The present invention also relates to the corresponding installation to implement the method.
Processes for Recovering Paraxylene
Disclosed is a process for recovering paraxylene in which a first simulated moving bed adsorption unit is used to produce two extract streams—one rich in paraxylene and a paraxylene-rich extract stream that is lean in ethylbenzene and an ethylbenzene-rich extract stream that is lean in paraxylene- and a paraxylene-depleted raffinate stream. A significant amount of the ethylbenzene is removed in the ethylbenzene-rich extract stream (at least enough to limit buildup in the isomerization loop), so the paraxylene-depleted raffinate stream may be isomerized in the liquid phase. Avoiding vapor phase isomerization saves energy and capital, as liquid phase isomerization requires less energy and capital than the vapor phase isomerization process due to the requirement of vaporizing the paraxylene-depleted stream and the use of hydrogen, which requires an energy and capital intensive hydrogen recycle loop.
System and process for recovering methane and carbon dioxide from biogas and reducing greenhouse gas emissions
Various illustrative embodiments of a system and process for recovering high-quality biomethane and carbon dioxide product streams from biogas sources and utilizing or sequestering the product streams are provided. The system and process synergistically yield a biomethane product which meets gas pipeline quality specifications and a carbon dioxide product of a quality and form that allows for its transport and sequestration or utilization and reduction in greenhouse gas emissions. The system and process result in improved access to gas pipelines for products, an improvement in the carbon intensity rating of the methane fuel, and improvements in generation of credits related to reductions in emissions of greenhouse gases.
System and process for recovering methane and carbon dioxide from biogas and reducing greenhouse gas emissions
Various illustrative embodiments of a system and process for recovering high-quality biomethane and carbon dioxide product streams from biogas sources and utilizing or sequestering the product streams are provided. The system and process synergistically yield a biomethane product which meets gas pipeline quality specifications and a carbon dioxide product of a quality and form that allows for its transport and sequestration or utilization and reduction in greenhouse gas emissions. The system and process result in improved access to gas pipelines for products, an improvement in the carbon intensity rating of the methane fuel, and improvements in generation of credits related to reductions in emissions of greenhouse gases.
MOBILE GAS PROCESSING PLANT
A mobile gas processing plant includes an inlet and an outlet, first and second Joule-Thompson (JT) valve units, an inlet scrubber, a dehydration unit including a contact tower, inlet and outlet filter separators, a vertical separator, and a dual pass line heater including first and second heating coils. The mobile gas processing plant is a mobile unit that is permanently mounted on at least one transport. The dehydration unit includes a contact tower that is permanently mounted on the at least one transport such that the contact tower is rotated up to be in an upright position relative to a base frame of the transport in an operational mode, and the contact tower is rotated down to be in a prostrated position relative to the base frame in a transportation mode. Each of the first and second JT valve units includes a first JT valve and a second JT valve. In the operational mode, and for each of the first and second JT valve units, a hydrocarbon gas stream flows through one of the first and second JT valves operating as a primary valve, and does not flow through the other of the first and second JT valves operating as a backup valve.