A process for hydrocracking a hydrocarbon feed is provided. The process comprises hydrocracking the hydrocarbon feed to produce a first hydrocracking product stream, separating the first hydrocracking product stream to form a gas stream and a liquid stream, hydrocracking the liquid stream to produce a second hydrocracking product stream, separating the second hydrocracking product stream to form a first light stream and a first heavy stream comprising benzene, toluene, xylene, C.sub.9+ hydrocarbon, or a combination comprising at least one of the foregoing, purifying the gas stream to form a purified gas stream, and separating the purified gas stream to form at least two of a hydrogen stream, C.sub.1 stream, C.sub.2 stream, C.sub.3 stream, C.sub.4 stream, C.sub.5+ stream, or a combination comprising at least one of the foregoing.

This invention describes a novel and efficient processing scheme that can be used to transform a vacuum residue feedstock into 0.5 wt % sulfur bunker fuel that fulfills the specifications required by the International Maritime Organization (IMO).

The present invention relates to a process for producing monoaromatic hydrocarbons from a hydrocarbon feed comprising polyaromatics, the process comprising contacting said feed in the presence of hydrogen with a M/A/zeolite catalyst under hydrocracking process conditions.

According to an embodiment of the present disclosure, petrochemicals may be produced from crude oil by a process which includes passing the crude oil and hydrogen into a hydroprocessing reactor, separating the hydrotreated oil into a lesser boiling point fraction and a greater boiling point fraction, passing the lesser boiling point fraction to a pyrolysis section of a steam cracker to produce a pyrolysis effluent comprising olefins, aromatics, or both, passing the greater boiling point fraction to a gasifier, where the gasifier produces hydrogen, and passing at least a portion of the hydrogen produced by the gasifier to the hydroprocessing reactor.

A method for optimising the operation of a facility for catalytic reforming, the facility including a multitude of reactors which have a catalyser and through which an operating gas including hydrocarbons and molecular hydrogen successively flows, wherein the composition of the operating gas in the reactors changes and wherein a product results at the outlet side of the last reactor. Specific constant characteristics as well as initial operating parameters that are present during the operation of the facility are acquired. A computational simulation of the chemical processes in the reactors then takes place, wherein results of a measurement of the chemical composition of the product at the outlet side of the last reactor is also included. A computational simulation of the chemical processes in the reactors with different varied operating parameters is subsequently carried out and set of optimised operating parameters is determined from the computed chemical composition.

Provided is a method for producing aromatic hydrocarbons from light alkanes. A light alkane feed is contacted with catalyst particles in each of reactors, wherein each of the reactors is a fluidized bed reactor and arranged in parallel with each other in a furnace. At least a portion of the alkane feed is converted to aromatic hydrocarbons using the catalyst particles, wherein the aromatic hydrocarbons form a part of a reactor effluent stream. The reactor effluent streams from each of the reactors are merged to form a first merged effluent stream. The first merged effluent stream is separated into the aromatic hydrocarbons, light hydrocarbons, and a fuel gas.

Methods and systems are provided for making gasoline. The method includes converting a resid-containing feed to a first fuel gas and a fluid coke in a fluidized bed reactor; gasifying the fluid coke with steam and air to produce a second fuel gas, said second fuel gas comprising a syngas; contacting the first fuel gas with a first conversion catalyst under first effective conversion conditions to form an effluent comprising C.sub.5+ hydrocarbon compounds; and converting the syngas to gasoline boiling range hydrocarbons by converting the syngas to a methanol intermediate product.

Treatment of hydrocarbon streams, and in one non-limiting embodiment refinery distillates, with reducing agents, such as borohydride and salts thereof, alone or together with at least one co-solvent results in reduction of the sulfur compounds such as disulfides, mercaptans, thiophenes, and thioethers that are present to give easily removed sulfides. In one non-limiting embodiment, the treatment converts the original sulfur compounds into hydrogen sulfide or low molecular weight mercaptans that can be extracted from the distillate with caustic solutions, hydrogen sulfide or mercaptan scavengers, solid absorbents such as clay or activated carbon or liquid absorbents such as amine-aldehyde condensates and/or aqueous aldehydes.

A method of processing a first material including an oil source, and a second material including a medium. The method includes mixing the first material and the second material to provide a blended feedstock mixture including predetermined respective proportions of the first material and the second material, and also including water. The blended feedstock mixture is heated in a pre-distillation process and is further heated in a distiller to at least partially crack and vaporize the oil source, to provide atmospheric gas oil and vacuum gas oil from the oil source, coked medium material including carbon-heavy hydrocarbons and sand, and a first barren hot medium material. The coked medium material is heated in a gasifier to provide a second barren hot medium material and syngas. Heat energy from certain products resulting from such heating is transferred to the blended feedstock mixture.

Carbon nanofiber doped alumina (Al-CNF) supported MoCo catalysts in hydrodesulfurization (HDS), and/or boron doping, e.g., up to 5 wt % of total catalyst weight, can improve catalytic efficiency. Al-CNF-supported MoCo catalysts, (Al-CNF-MoCo), can reduce the sulfur concentration in fuel, esp. liquid fuel, to below the required limit in a 6 h reaction time. Thus, Al-CNF-MoCo has a higher catalytic activity than AlMoCo, which may be explained by higher mesoporous surface area and better dispersion of MoCo metals on the AlCNF support relative to alumina support. The BET surface area of AlMoCo may be 75% less than Al-CNF-MoCo, e.g., 166 vs. 200 m.sup.2/g. SEM images indicate that the catalyst nanoparticles can be evenly distributed on the surface of the CNF. The surface area of the AlMoCoB5% may be 206 m.sup.2/g, which is higher than AlMoCoB0% and AlMoCoB2%, and AlMoCoB5% has the highest HDS activity, removing more than 98% sulfur and below allowed levels.