Patent classifications
C10G57/00
PROCESS TO IMPROVE THE STABILITY OF THERMALLY CRACKED PETROLEUM PRODUCTS
A process for forming a petroleum product includes introducing a feed stream of a petroleum feedstock to a supercritical water reactor. The feed stream is reacted with supercritical water in the supercritical water reactor, thereby forming a supercritical water reactor effluent. The supercritical water reactor effluent is introduced to a separator to separate the supercritical water reactor effluent into a light stream and a heavy stream. At least a portion of the light stream is introduced to a reformer to concentrate aromatics in the at least a portion of the light stream, thereby forming a reformer effluent. The reformer effluent is mixed with the heavy stream.
PROCESS TO IMPROVE THE STABILITY OF THERMALLY CRACKED PETROLEUM PRODUCTS
A process for forming a petroleum product includes introducing a feed stream of a petroleum feedstock to a supercritical water reactor. The feed stream is reacted with supercritical water in the supercritical water reactor, thereby forming a supercritical water reactor effluent. The supercritical water reactor effluent is introduced to a separator to separate the supercritical water reactor effluent into a light stream and a heavy stream. At least a portion of the light stream is introduced to a reformer to concentrate aromatics in the at least a portion of the light stream, thereby forming a reformer effluent. The reformer effluent is mixed with the heavy stream.
Methods and systems to produce needle coke from aromatic recovery complex bottoms
Provided here are systems and methods of production of needle coke by processing an aromatic rejects stream containing long chain alkyl monoaromatics and bridged diaromatics through a delayed coking process. Various other embodiments may be disclosed and claimed.
Systems and processes integrating fluidized catalytic cracking with metathesis for producing olefins
Processes for producing olefins include introducing a hydrocarbon feed to a high-severity fluidized catalytic cracking system, contacting the hydrocarbon feed with a cracking catalyst under high-severity conditions in the high-severity fluidized catalytic cracking system to produce a cracking reaction effluent comprising butene, and passing at least a portion of the cracking reaction effluent, which includes at least butene, to a metathesis system. The processes further include contacting the portion of the cracking reaction effluent with a metathesis catalyst in the metathesis system, which causes at least a portion of the butene in the cracking C4 effluent to undergo a metathesis reaction to produce a metathesis reaction effluent comprising at least one of ethylene, propene, or both. The processes may further include separating a metathesis C5+ effluent from the metathesis reaction effluent and passing the metathesis C5+ effluent back to the high-severity fluidized catalytic cracking unit.
Systems and processes integrating fluidized catalytic cracking with metathesis for producing olefins
Processes for producing olefins include introducing a hydrocarbon feed to a high-severity fluidized catalytic cracking system, contacting the hydrocarbon feed with a cracking catalyst under high-severity conditions in the high-severity fluidized catalytic cracking system to produce a cracking reaction effluent comprising butene, and passing at least a portion of the cracking reaction effluent, which includes at least butene, to a metathesis system. The processes further include contacting the portion of the cracking reaction effluent with a metathesis catalyst in the metathesis system, which causes at least a portion of the butene in the cracking C4 effluent to undergo a metathesis reaction to produce a metathesis reaction effluent comprising at least one of ethylene, propene, or both. The processes may further include separating a metathesis C5+ effluent from the metathesis reaction effluent and passing the metathesis C5+ effluent back to the high-severity fluidized catalytic cracking unit.
Circular economy for plastic waste to polyethylene and chemicals via refinery crude unit
Provided is a continuous process for converting waste plastic into recycle for polyethylene polymerization or for normal alpha olefins. The process comprises selecting waste plastics containing polyethylene and/or polypropylene and then passing the waste plastics through a pyrolysis reactor to thermally crack at least a portion of the polyolefin waste and produce a pyrolyzed effluent. The pyrolyzed effluent is separated into offgas, a naphtha/diesel fraction, a heavy fraction, and char. The naphtha/diesel fraction is passed to a crude unit in a refinery from which is recovered a straight run naphtha fraction (C.sub.5-C.sub.8) or a propane/butane (C.sub.3-C.sub.4) fraction. The straight run naphtha fraction, or propane and butane (C.sub.3-C.sub.4) fraction, is passed to a steam cracker for ethylene production. The ethylene is converted to normal alpha olefin and/or polyethylene. Also, a heavy fraction from the pyrolysis reactor can be combined with a heavy fraction of normal alpha olefin stream recovered from the steam cracker. The combined heavy fraction and heavy fraction of normal alpha olefin stream can be passed to a wax hydrogenation zone to produce wax.
FCC CO-PROCESSING OF BIOMASS OIL
Systems and methods are provided for co-processing of biomass oil in a fluid catalytic cracking (FCC) system that include recovering an additional source of H.sub.2 or synthesis gas from the overhead product gas stream. The additional H.sub.2 can be used to partially hydrogenate biomass oil prior to co-processing the biomass oil in the fluid catalytic cracking system. Additionally or alternately, the additional synthesis gas can represent an additional yield of products from the process, such as an additional yield that can be used for synthesis of further liquid products.
INTEGRATED PRODUCTION OF HYDROGEN, PETROCHEMICALS, AND POWER
A processing facility is provided. The processing facility includes an asphaltenes and metals (AM) removal system configured to process a feed stream to produce a power generation stream, a hydroprocessing feed stream, and an asphaltenes stream. A power generation system is fed by the power generation feed stream. A hydroprocessing system is configured to process the hydroprocessing feed stream to form a gas stream and a liquid stream. A hydrogen production system is configured to produce hydrogen, carbon monoxide and carbon dioxide from the gas feed stream. A carbon dioxide conversion system is configured to produce synthetic hydrocarbons from the carbon dioxide, and a cracking system is configured to process the liquid feed stream.
Optimizing the simultaneous production of high-value chemicals and fuels from heavy hydrocarbons
Methods and systems for producing light olefins are disclosed. A feedstock comprising crude oil is distilled to produce a plurality of streams including a naphtha stream and a vacuum residue stream. The naphtha is fed to a steam cracking unit to produce light olefins, C.sub.4 hydrocarbons, pyrolysis gasoline and pyrolysis oil. The vacuum residue stream is hydrocracked to produce additional naphtha and heavy unconverted oil. The heavy unconverted oil and the pyrolysis oil from steam cracking unit can be deasphalted to produce deasphalted oil and pitch product. The deasphalted oil can be further hydrocracked to produce naphtha. The pitch product can be gasified to produce synthesis gas, which is further used to produce methanol. The methanol can be used to react with isobutylene of the C.sub.4 hydrocarbon stream from steam cracker to produce methyl tert-butyl ether (MTBE).
Process for separating alkylation product, alkylation reaction and separation process, and related apparatus
A liquid phase alkylation product from an alkylation reaction unit is introduced into a first heat-exchanger directly or after being pressurized with a pressure pump and heat-exchanged with a vapor phase stream from the column top of a high-pressure fractionating column n, then introduced into a second heat-exchanger and further heated to 100° C.-150° C., then introduced into the high-pressure fractionating column and subjected to fractionation at 2.0 MPa-4.0 MPa, the vapor phase stream from the column top of the high-pressure fractionating column is heat-exchanged with the liquid phase alkylation product to be separated, a liquid phase stream from the column bottom of the high-pressure fractionating column is introduced into a low-pressure fractionating column and subjected to fractionation under at 0.2 MPa-1.0 MPa, a low-carbon alkane is obtained from the column top of the low-pressure fractionating column n, and a liquid phase stream obtained from the column bottom of the low-pressure fractionating column is an alkylation oil product.