This application relates to renewable diesel production and to production of renewable naphtha in a renewable diesel unit. Disclosed herein is an example of a method of renewable diesel production. Examples embodiments of the method may include hydrotreating the biofeedstock by reaction with hydrogen to form a hydrotreated biofeedstock; contacting at least a portion of the hydrotreated biofeedstock with a dewaxing catalyst to produce a renewable diesel product and a renewable naphtha product; separating the renewable diesel product and the renewable naphtha product in a product splitter; and monitoring an octane number of the renewable naphtha product with an analyzer.

This application relates to renewable diesel production and to production of renewable naphtha in a renewable diesel unit. Disclosed herein is an example of a method of renewable diesel production. Examples embodiments of the method may include hydrotreating the biofeedstock by reaction with hydrogen to form a hydrotreated biofeedstock; contacting at least a portion of the hydrotreated biofeedstock with a dewaxing catalyst to produce a renewable diesel product and a renewable naphtha product; separating the renewable diesel product and the renewable naphtha product in a product splitter; and monitoring an octane number of the renewable naphtha product with an analyzer.

Systems and methods are provided for hydroprocessing of bio-derived feeds, such as bio-oils and/or other types of feeds including triglycerides, fatty acids, and/or fatty acid derivatives. The systems and methods can assist with maintaining a desired temperature profile within a reactor while performing hydroprocessing on a feed with substantial oxygen content. In various aspects, the initial bed of the reactor can be exposed to 30 vol % or less of the total fresh feed. The remaining portions of the fresh feed can be introduced below one or more of the catalyst beds in the reactor. By reducing or minimizing the amount of fresh feed introduced upstream from the initial catalyst bed that contains a catalyst with hydrodeoxygenation activity, the net amount of product recycle can be reduced or minimized while still maintaining a target temperature profile across individual catalyst beds and/or across the reactor.

According to at least one aspect of the present disclosure, a method for processing a heavy oil includes introducing the heavy oil to a hydroprocessing unit, the hydroprocessing unit being operable to hydroprocess the heavy oil to form a hydroprocessed effluent by contacting the heavy oil feed with an HDM catalyst, an HDS catalyst, and an HDA catalyst. The hydroprocessed effluent is passed directly to a HS-FCC unit, the HS-FCC unit being operable to crack the hydroprocessed effluent to form a cracked effluent comprising at least one product. The cracked effluent is passed out of the HS-FCC unit. The heavy oil has an API gravity of from 25 degrees to 50 degrees and at least 20 wt. % of the hydroprocessed effluent passed to the HS-FCC unit has a boiling point less than 225 degrees ° C.

Processes herein may be used to thermally crack various hydrocarbon feeds, and may eliminate the refinery altogether while making the crude to chemicals process very flexible in terms of crude. In embodiments herein, crude is progressively separated into light and heavy fractions utilizing convection heat from heaters used in steam cracking. Depending on the quality of the light and heavy fractions, these are routed to one of three upgrading operations, including a fixed bed hydroconversion unit, a fluidized catalytic conversion unit, or a residue hydrocracking unit that may utilize either an ebullated bed reactor with extrudate catalysts or a slurry hydrocracking reactor using a homogeneous catalyst system, such as a molybdenum based catalysts which may optionally be promoted with nickel. Products from the upgrading operations can be finished olefins and/or aromatics, or, for heavier products from the upgrading operations, may be used as feed to the steam cracker.

A method for preparing a high-quality fuel oil and/or chemical raw material from a biomass pyrolysis liquid. In the method, a biomass pyrolysis liquid undergoes a hydrodeoxygenation reaction in a catalyst full mixing flow circulation system in a fluidized bed reactor to obtain deoxygenated oil, and the obtained deoxygenated oil undergoes a hydrocracking reaction in a fixed bed reactor to obtain high-quality fuel oil and/or a chemical raw material. The method may prevent the condensation and coking of a biomass pyrolysis liquid, solve the problem of rapid catalyst deactivation, and may convert a biomass pyrolysis liquid into a high-quality fuel oil that may be directly used by vehicles and into a chemical product.

A syngas generator is disclosed as an exothermic gas generator that can accommodate high combustion temperatures of a natural gas/oxygen flame. The generator consists of four sections: a heavily insulated combustion chamber, a catalyst chamber, a spray chamber, and a heat exchanger. These four sections may be arranged in series and tightly bolted together to form a gas-tight system. Natural gas, oxygen and steam are supplied to a burner at the inlet end of the combustion chamber. This mixture is ignited and the resulting hot process gas is then fed into a catalyst bed where it reacts with the steam and is converted to carbon monoxide and hydrogen (syngas). The syngas is fed to a Fischer-Tropsch unit to create liquid fuel.

A syngas generator is disclosed as an exothermic gas generator that can accommodate high combustion temperatures of a natural gas/oxygen flame. The generator consists of four sections: a heavily insulated combustion chamber, a catalyst chamber, a spray chamber, and a heat exchanger. These four sections may be arranged in series and tightly bolted together to form a gas-tight system. Natural gas, oxygen and steam are supplied to a burner at the inlet end of the combustion chamber. This mixture is ignited and the resulting hot process gas is then fed into a catalyst bed where it reacts with the steam and is converted to carbon monoxide and hydrogen (syngas). The syngas is fed to a Fischer-Tropsch unit to create liquid fuel.

A coke catching apparatus for use in hydrocarbon cracking to assist in the removal of coke and the prevention of coke build up in high coking hydrocarbon processing units. The apparatus includes a grid device for preventing large pieces of coke from entering the outlet of the process refining equipment while allowing small pieces of coke to pass through and be disposed of. The coke catching apparatus can be easily disassembled to be removed from the refining process equipment and cleaned.

A coke catching apparatus for use in hydrocarbon cracking to assist in the removal of coke and the prevention of coke build up in high coking hydrocarbon processing units. The apparatus includes a grid device for preventing large pieces of coke from entering the outlet of the process refining equipment while allowing small pieces of coke to pass through and be disposed of. The coke catching apparatus can be easily disassembled to be removed from the refining process equipment and cleaned.