Systems and methods for producing light olefins and BTX (benzene, toluene, and xylene). Crude oil is first separated to produce light naphtha and heavy naphtha. Light naphtha is fed to a steam cracking unit and heavy naphtha is fed to a catalytic cracking unit. The effluent from the steam cracking unit and the effluent from the catalytic cracking unit are flowed into an oil quench tower and are further separated in a separation unit to produce an ethylene stream, a propylene stream, and a BTX stream. The C.sub.4 hydrocarbons, ethane, and propane from the effluent of the steam cracking unit and the effluent from the catalytic cracking unit are recycled to the steam cracking unit. The non-BTX C.sub.6+ hydrocarbons from the effluent of the steam cracking unit and the effluent from the catalytic cracking unit are recycled to the catalytic cracking unit.

A process for treating effluent streams in a naphtha complex is described. One or more of the sour water stripping unit for the NHT sour water from the NHT, the amine treatment unit and the caustic treatment unit for the NHT stripper off-gas, the caustic scrubber unit or other chloride treatment unit for the off-gas from the C.sub.5-C.sub.6 isomerization zone and the C.sub.4 isomerization zone, and the caustic scrubber unit or other chloride treatment unit for the regenerator off-gas are replaced with a thermal oxidation system.

The invention relates to a method including a system of additives which increase fluidity and/or flow capacity and minimize pressure drops from the steps of lifting in production wells, collection lines, dehydration systems and ducts for transporting heavy and extra-heavy hydrocarbons. In addition, the injected system of chemical additives increases the dilution capacity of the solvents that need to be applied to improve the quality of the crude oil (reduce viscosity and density, and increase API gravity), thereby facilitating the dehydration and transport.

Catalyst containing an active phase which contains a group VIB element, at least one group VIII element and phosphorus, and a support containing alumina, the catalyst being characterized in that at least 80% by weight of the group VIB elements, of the group VIII elements and of the phosphorus are distributed in the form of a crust at the periphery of said support, the thickness of said crust being between 100 and 1200 μm, the content of group VIB element being between 1% and 8% by weight relative to the total weight of the catalyst, the content of group VIII element being between 0.5% and 5% by weight relative to the total weight of the catalyst, and the content of phosphorus being between 0.2% and 3% by weight relative to the total weight of the catalyst, and the support having a specific surface area of between 100 m.sup.2/g and 250 m.sup.2/g.

A process for estimating catalyst performance of catalyst used in refinery reforming processes for converting naphtha to gasoline. More in particular, the catalyst to be investigated is subjected to analysis in parallel over time at a temperature to achieve a desired RON on yield of e.g. C5+, for at least two different reaction times. The reactions are terminated after which coke deposition is determined, and relationships of coke deposition and yield, both as a function of reaction temperature for the catalyst used are established, thereby enabling comparison of catalyst performance as determined by a yield-temperature relationship at a given coke deposition degree.

A process for upgrading a hydrocarbon feed includes passing the hydrocarbon feed and an aromatic bottoms stream to an FCC unit including an FCC reactor and a catalyst regenerator. The hydrocarbon feed is hydrogen-rich having at least 12 wt. % hydrogen, and the aromatic bottoms stream is a bottoms stream produced from an aromatics recovery complex for processing reformate from naphtha reforming. The hydrocarbon feed and aromatic bottoms stream are cracked over the FCC catalysts to produce an effluent and spent FCC catalysts having coke deposits. The spent FCC catalyst is regenerated through combustion of the coke deposits. The hydrogen-rich hydrocarbon feed does not produce enough coke to satisfy the heat demand of the FCC reactor. Cracking the aromatic bottoms stream increases the amount of coke so that combustion of the additional coke during regeneration produces additional heat to satisfy the heat demand of the FCC reactor.

Provided are novel process for upgrading naphtha and increasing the yield of reformate. Olefinic naphtha and light paraffins are combined and fed to a catalytic fluidized bed reactor maintained at a temperature about 775° F. and about 1250° F. and an operating pressure between about 10 psig and about 500 psig to produce a product comprising at least 1 wt. % higher C.sub.5+ hydrocarbon than the combined feed and at least 55 wt. % aromatics.

Processes and systems for controlling operation of a commercial refinery distillation column and/or splitter operable to separate hydrocarbons. An automated process controller (APC) receives signal from at least one analyzer that provides information about the concentration of at least a first chemical in a first fraction and a second chemical in a second fraction obtained from the distillation column. The APC comprises programming in the form of an algorithm that calculates real-time monetary values for the first chemical and the second chemical and alters the operation of the distillation column to change either the percentage of the first chemical in the second fraction or the percentage of the second chemical in the first fraction, thereby maximizing overall operational profit for the distillation column.

The invention is a process for producing a white oil having an initial boiling point of at least 300° C., the process comprising a step of catalytically hydrogenating a hydrocarbon feedstock at a temperature of from 80 to 190° C., at a pressure of from 50 to 160 bars, a liquid hourly space velocity of 0.2 to 5 hr.sup.−1 and an hydrogen treat rate up to 200 Nm.sup.3/ton of feed, the hydrocarbon feedstock having a sulphur content of less than 10 ppm by weight, an initial boiling point within the range from 150 to 350° C. and a final boiling point within the range from 350 to 550° C.

A multi-stage process for the production of an ISO 8217 compliant Product Heavy Marine Fuel Oil from ISO 8217 compliant Feedstock Heavy Marine Fuel Oil involving a Reaction System composed of one or more reactor vessels selected from a group reactor wherein said one or more reactor vessels contains one or more reaction sections configured to promote the transformation of the Feedstock Heavy Marine Fuel Oil to the Product Heavy Marine Fuel Oil. The Product Heavy Marine Fuel Oil has a Environmental Contaminate level has a maximum sulfur content (ISO 14596 or ISO 8754) between the range of 0.05 mass % to 1.0 mass. A process plant for conducting the process for conducting the process is disclosed that can utilize a modular reactor vessel.