A method of generating a reaction product from a feedstock via a centrifuge reactor that includes introducing a flow of feedstock to a centrifuge reactor, the centrifuge reactor including: a central rotational axis X, and a centrifuge assembly having a reaction chamber with the centrifuge assembly configured to rotate about the central rotational axis X. The method further includes rotating the centrifuge assembly about the central rotational axis X at a tip speed to generate an acceleration gradient from the central rotational axis X and from a first reaction chamber end to a second reaction chamber end and generating reaction conditions in the reaction chamber, the reaction conditions and acceleration gradient causing a separation of products from a reaction of the feedstock within the reaction chamber.

Systems and methods are provided for processing of challenged feedstocks to produce distillate fuel products, such as jet boiling range products and/or diesel boiling range products. The challenged feedstocks can have a high aromatics content, a low API gravity, and/or a low cetane index/cetane number. A feedstock can be processed to form distillate fuel products by processing the feedstock in reaction system including at least two stages. The first stage can perform an initial amount of hydrotreating and/or hydrocracking, while the second stage can include exposing a portion of the hydrotreated and/or hydrocracked effluent to a USY catalyst including a supported noble metal. The USY catalyst can have a desirable combination of catalyst properties. Processing a challenged feedstock in a second stage with the USY catalyst having a desirable combination of properties can allow for production of an increased yield of distillate fuel from the challenged feedstock.

A process to convert paraffinic feedstocks into renewable poly-alpha-olefins (PAO) basestocks. In a preferred embodiment of the invention, renewable feed comprising triglycerides and/or free fatty acids are hydrotreated producing an intermediate paraffin feedstock. This paraffin feedstock is thermally cracked into a mixture of olefins and paraffins comprising linear alpha olefins. The olefins are separated and the un-reacted paraffins are recycled to the thermal cracker. Light olefins preferably (C2-C6) are oligomerized with a surface deactivated zeolite producing a mixture of slightly branched oligomers comprising internal olefins. The heavier olefins (C6-C16) are oligomerized, preferably with a BF3 catalyst and co-catalyst to produce PAO products. The oligomerized products can be hydrotreated and distilled together or separate to produce finished products that include naphtha, distillate, solvents, and PAO lube basestocks.

Processes for converting methane and/or other hydrocarbons to synthesis gas (i.e., a gaseous mixture comprising H.sub.2 and CO) are disclosed, in which at least a portion of the hydrocarbon(s) is reacted with CO.sub.2. At least a second portion of the methane may be reacted with H.sub.2O (steam), thereby improving overall thermodynamics of the process, in terms of reducing endothermicity (ΔH) and the required energy input, compared to “pure” dry reforming in which no H.sub.2O is present. Such dry reforming (reaction with CO.sub.2 only) or CO.sub.2-steam reforming (reaction with both CO.sub.2 and steam) processes are advantageously integrated with Fischer-Tropsch synthesis to yield liquid hydrocarbon fuels. Further integration may involve the use of a downstream finishing stage involving hydroisomerization to remove FT wax. Yet other integration options involve the use of combined CO.sub.2-steam reforming and FT synthesis stages (optionally with finishing) for producing liquid fuels from gas streams generated in a number of possible processes, including the hydropyrolysis of biomass.

The present technology provides compositions that include at least about 98 weight percent (“wt %”) n-paraffins which, among other surprising features, may be suitable for use as a diesel fuel, an aviation fuel, a jet fuel blendstock, a blendstock to reduce the cloud point of a diesel fuel, a fuel for portable heaters, and/or as a charcoal lighter fluid. The composition includes at least about 98 wt % C.sub.7-C.sub.12 n-paraffins, where at least about 10 wt % of composition includes n-decane, at least about 20 wt % of the composition includes n-dodecane, and at least about 75 wt % of the composition includes even carbon number paraffins. The composition also includes less about 0.1 wt % oxygenates and less than about 0.1 wt % aromatics. The composition may be produced by a process that includes hydrotreating a biorenewable feedstock comprising at least one of palm kernel oil, coconut oil, babassu oil, microbial oil, or algal oil.

An apparatus is provided for processing reusable fuel comprising a first-type cyclone cooler having a first configuration. The apparatus also provides one or more second-type cyclone coolers, wherein each one or more second-type cyclone coolers has a substantially identical second configuration to respective other one or more second-type cyclone coolers, wherein the second configuration is different than the first configuration. The apparatus may also provide an air cooled heat exchanger, a coil condenser and one or more bubblers. The first-type cyclone cooler and the one or more second-type cyclone coolers are connected. One of the one or more second-type cyclone coolers is connected to the air cooled heat exchanger. The air cooled heat exchanger is connected to the coil condenser. The coil condenser is connected to the one or more bubblers.

A process and device for reducing the environmental contaminants in a ISO 8217 compliant Feedstock Heavy Marine Fuel Oil, the process involving: mixing a quantity of the Feedstock Heavy Marine Fuel Oil with a quantity of Activating Gas mixture to give a feedstock mixture; contacting the feedstock mixture with one or more catalysts to form a Process Mixture from the feedstock mixture; separating the Product Heavy Marine Fuel Oil liquid components of the Process Mixture from the gaseous components and by-product hydrocarbon components of the Process Mixture and, discharging the Product Heavy Marine Fuel Oil. The Product Heavy Marine Fuel Oil is compliant with ISO 821 7 for residual marine fuel oils and has a sulfur level has a maximum sulfur content (ISO 14596 or ISO 8754) between the range of 0.05% wt. to 0.5% wt. The Product Heavy Marine Fuel Oil can be used as or as a blending stock for an ISO 8217 compliant, IMO MARPOL Annex VI (revised) compliant low sulfur or ultralow sulfur heavy marine fuel oil.

An integrated refinery process for removing mercaptans from a hydrocarbon stream containing mercaptans and converting by-product disulfide oil to useful products. The process includes introducing the hydrocarbon stream containing mercaptans into an extraction vessel containing an alkaline solution and passing the hydrocarbon stream through an extraction section of the extraction vessel which includes one or more liquid-liquid contacting decks for reaction to convert the mercaptans to alkali metal alkanethiolates. Further, the process includes withdrawing a hydrocarbon product stream free of mercaptans from the extraction vessel and recovering spent caustic containing alkali metal alkanethiolates from the extraction vessel. Additionally, the process includes subjecting the spent caustic containing alkali metal alkanethiolates to air oxidation to produce a by-product stream containing disulfide oils (DSO) and sulfides and processing the by-product stream in a steam cracking unit to produce a DSO free product stream.

A system for processing a stream including fuel oil includes an atmospheric flash column for receiving the stream as feedstock and separate the stream into an atmospheric flash distillate stream and an atmospheric flash residue stream. The system includes a vacuum flash column for receiving the atmospheric flash residue stream and separating the atmospheric flash residue stream into a vacuum flash distillate stream, a vacuum flash residue stream, and a vacuum gas oil stream. The system includes a first hydrocracking unit for receiving and processing at least a portion of the vacuum flash residue stream to produce an intermediate stream and a slurry. The system includes a second hydrocracking unit for receiving and processing the vacuum gas oil stream and the intermediate stream to produce a naphtha product and a light ends product. The system includes a pelletization unit for receiving and processing the slurry to produce a pelletized product.

In a hydrocracking process, the product from the first stage reactor passes through a steam stripper to remove hydrogen, H.sub.2S, NH.sub.3, light gases (C.sub.1-C.sub.4), naphtha and diesel products. The stripper bottoms are separated from hydrogen, H.sub.2S, NH.sub.3, light gases (C.sub.1-C.sub.4), naphtha, and diesel products and treated in a second stage reactor. The effluent stream from the second stage reactor, along with the stream of separated hydrogen, H.sub.2S, NH.sub.3, light gases (C.sub.1-C.sub.4), naphtha, and diesel products, are passed to a separation stage for separating petroleum fractions. Preferably, the effluent stream from the first stage reactor is passed through a steam generator prior to the steam stripping step. In an alternate embodiment, the effluent stream from the first stage reactor is passed through a vapor/liquid separator stripper vessel prior to the steam stripping step.