Processes for upgrading a hydrocarbon. The process can include (I) contacting a hydrocarbon-containing feed with a catalyst that can include a Group 8-10 element or a compound thereof disposed on a support to effect conversion of the hydrocarbon-containing feed to produce a coked catalyst and an effluent. The process can also include (II) contacting the coked catalyst with an oxidant to effect combustion the coke to produce a regenerated catalyst. The process can also include (IIa) contacting the regenerated catalyst with a reducing gas to produce a regenerated and reduced catalyst. The process can also include (III) contacting an additional quantity of the hydrocarbon-containing feed with the regenerated and reduced catalyst. A cycle time from the contacting the hydrocarbon-containing feed with the catalyst in step (I) to the contacting the additional hydrocarbon-containing feed with the regenerated and reduced catalyst in step (III) can be ≤1 hours.

Metal nanoparticle-deposited, nitrogen-doped carbon adsorbents are disclosed, along with methods of removing sulfur compounds from a hydrocarbon feed stream using these adsorbents.

The present disclosure relates to a process for reducing the amount of carbon disulphide (CS.sub.2) in a hydrocarbon feed containing C.sub.5-C.sub.8 fractions. The hydrocarbon feed is treated with an amine functionalized anion exchange resin (basic anion exchange resin) to obtain a mixture comprising a liquid fraction containing treated hydrocarbon and a solid mass containing an adduct of CS.sub.2 and the amine functionalized anion exchange resin. The so obtained liquid fraction containing the treated hydrocarbon is separated from the solid mass to obtain the hydrocarbon having CS.sub.2 content less than 2 ppm. The amine functionalized anion exchange resin can be regenerated from the solid mass.

A process and a system are used for production of multiple grades of ultralow aromatic solvents/chemicals having preferred boiling range, flash point and viscosity from different hydrocarbon streams. A plurality of hydrotreating steps are used to hydrotreat a plurality of hydrocarbon feedstocks in the presence of a hydrogen gas stream and a catalyst system. Further, at least one dissolved gas stripping step, at least one adsorption step, and a distillation step are included in the process. Desired iso-paraffin molecules are thereby preserved, and the undesired aromatic molecules are converted into desired naphthene molecules.

A process and a system are used for production of multiple grades of ultralow aromatic solvents/chemicals having preferred boiling range, flash point and viscosity from different hydrocarbon streams. A plurality of hydrotreating steps are used to hydrotreat a plurality of hydrocarbon feedstocks in the presence of a hydrogen gas stream and a catalyst system. Further, at least one dissolved gas stripping step, at least one adsorption step, and a distillation step are included in the process. Desired iso-paraffin molecules are thereby preserved, and the undesired aromatic molecules are converted into desired naphthene molecules.

Materials and methods for mitigating the effects of halide species contained in process streams are provided. A halide-containing process stream can be contacted with mitigation materials comprising active metal oxides and a non-acidic high surface area carrier combined with a solid, porous substrate. The halide species in the process stream can be reacted with the mitigation material to produce neutralized halide salts and a process stream that is essentially halide-free. The neutralized salts can be attracted and retained on the solid, porous substrate.

A regeneration method for a liquefied gas thiol-removing alkaline solution comprising the following steps: performing an oxygenation reaction with respect to a liquefied gas thiol-removing alkaline solution and, at the same time, utilizing a high air-liquid condition to extract a disulfide and a polysulfide into a gas phase, thus completing the separation of the disulfide and the polysulfide from the alkaline solution, and implementing the regeneration of the liquefied gas thiol-removing alkaline solution.

Methods and systems for manufacturing lubrication oils are disclosed. In one embodiment, a method for manufacturing a lubrication oil includes the steps of receiving into an adsorber unit an unconverted oil (UCO) feedstock comprising five and six ring polynuclear aromatic (PNA) compounds and contacting the UCO feedstock with an adsorbent to remove PNA compounds, thereby forming a treated UCO feedstock with a low concentration of five and six ring PNAs.

A multi-stage process for the production of an ISO8217 compliant Product Heavy Marine Fuel Oil from ISO 8217 compliant Feedstock Heavy Marine Fuel Oil involving a core process under reactive conditions in a Reaction System composed of one or more reaction vessels, wherein one or more of the reaction vessels contains one or more catalysts in the form of a structured catalyst bed and is operated under reactive distillation conditions. The Product Heavy Marine Fuel Oil has a sulfur 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.

Methods are provided for treatment of kerosene/jet fuel boiling range fractions, such as previously qualified jet fuel fractions, to allow blending of the kerosene/jet fuel boiling range fractions to produce a jet fuel boiling range blend having a breakpoint that is equal to or greater than the breakpoint of at least one of the kerosene jet fuel boiling range fractions used to form the blend. The breakpoint of the jet fuel boiling range blend can be maintained by treating at least one of the component fractions of the blend and/or by treating the blend to reduce a nitrogen content. The reduced nitrogen content can correspond to a reduced content of total nitrogen and/or a reduced content of unexpected nitrogen compounds.