Biomass is converted into a bio-oil containing stream in a riser reactor containing a cooling media. The cooling media quenches the rapid heat transfer to the biomass during cracking of the biomass in the mixing zone of the riser. By lowering the temperature to which the mixing zone effluent is exposed, production of carbon monoxide and light gases is decreased during thermolysis of the biomass.

A catalyst and its use for selectively desulfurizing sulfur compounds present in an olefin-containing hydrocarbon feedstock to very low levels with minimal hydrogenation of olefins. The catalyst comprises an inorganic oxide substrate containing a nickel compound, a molybdenum compound and optionally a phosphorus compound, that is overlaid with a molybdenum compound and a cobalt compound. The catalyst is further characterized as having a bimodal pore size distribution with a large portion of its total pore volume contained in pores having a diameter less than 250 angstroms and in pores having a diameter greater than 1000 angstroms.

The present invention relates to a process for converting mixed waste plastic into liquid fuels by catalytic cracking. The process comprises the steps of introducing mixed waste plastic and a catalyst comprising an amorphous-type catalyst within a reactor; allowing at least a portion of the mixed waste plastic to be converted to liquid fuels within the reactor; and removing a product stream containing said liquid fuels from the reactor.

Embodiments provide a method and apparatus for recovering components from a hydrocarbon feedstock. According to at least one embodiment, the method includes supplying a hydrocarbon feedstock to an oxidation reactor, wherein the hydrocarbon feedstock is oxidized in the presence of a catalyst under conditions sufficient to selectively oxidize sulfur compounds and nitrogen compounds present in the hydrocarbon feedstock, separating the hydrocarbons, the oxidized sulfur compounds, and the oxidized nitrogen compounds by solvent extraction, collecting a residue stream that includes the oxidized sulfur compounds and the oxidized nitrogen compound, and supplying the first residue stream to a fluid catalytic cracking unit. The first residue stream is further supplied through a hydrotreater prior to supplying the first residue stream to the fluid catalytic cracking unit.

The present disclosure includes a system for producing low carbon olefins and/or aromatics from raw material comprising naphtha. The system can include a reaction unit that includes a fast fluidized bed reactor, a stripping unit that includes a stripper, and a regeneration unit. The reactor unit is adapted to allow the catalytic cracking of naphtha and to output reaction unit effluent material (spent catalyst and product gas) into the stripping unit, which is adapted to output product gas. The stripping unit is connected to and in fluid communication with the regeneration unit such that the stripping unit supplies the spent catalyst from the reaction unit to regeneration unit. The regeneration unit is adapted to regenerate the spent catalyst to form regenerated catalyst. The regeneration unit is connected to and in fluid communication with the fast fluidized bed reactor such that, in operation, regenerated catalyst can be sent to the fast fluidized bed reactor of the reaction unit.

A process is presented for the management of sulfur on a catalyst. The catalyst is a dehydrogenation catalyst, and sulfur accumulates during the dehydrogenation process. Sulfur compounds are stripped from the spent catalyst and the catalyst is cooled before the regeneration process. The process includes controlling the amount of sulfur that needs to be removed from the catalyst before regeneration.

A process is presented for the management of sulfur on a catalyst. The catalyst is a dehydrogenation catalyst, and sulfur accumulates during the dehydrogenation process. Sulfur compounds are stripped from the spent catalyst and the catalyst is cooled before the regeneration process. The process includes controlling the amount of sulfur that needs to be removed from the catalyst before regeneration.

A system including a mixing apparatus configured to produce a reformer feedstock and comprising one or more cylindrical vessel having a conical bottom section, an inlet for superheated steam within the conical bottom section and an inlet for at least one carbonaceous material at or near the top of the cylindrical vessel, wherein the one or more cylindrical vessel is a pressure vessel configured for operation at a pressure in the range of from about 5 psig (34.5 kPa) to about 50 psig (344.7 kPa); a reformer configured to produce, from the reformer feedstock, a reformer product comprising synthesis gas, and also producing a hot flue gas; a synthesis gas conversion apparatus configured to catalytically convert at least a portion of the synthesis gas in the reformer product into synthesis gas conversion product, and to separate, from the synthesis gas conversion product, a spent catalyst stream and a tailgas.

A process for prolonging catalyst activity may comprise contacting heavy hydrocarbon feedstock, wherein the heavy hydrocarbon feedstock is essentially free of residue, and hydrogen with catalyst in a hydroprocessing unit operating at a pressure of greater than or equal to 100 bars. The process may further comprise performing hydrocracking, hydrodesulfurization, and hydrodenitrogenation in a single stage of the hydroprocessing unit to create a hydroprocessed effluent. The process may further comprise regenerating spent catalyst in a catalyst regeneration unit. Additionally, the process may further comprise passing regenerated catalyst back to the hydroprocessing unit without rejuvenating the spent catalyst.

A process for prolonging catalyst activity may comprise contacting heavy hydrocarbon feedstock, wherein the heavy hydrocarbon feedstock is essentially free of residue, and hydrogen with catalyst in a hydroprocessing unit operating at a pressure of greater than or equal to 100 bars. The process may further comprise performing hydrocracking, hydrodesulfurization, and hydrodenitrogenation in a single stage of the hydroprocessing unit to create a hydroprocessed effluent. The process may further comprise regenerating spent catalyst in a catalyst regeneration unit. Additionally, the process may further comprise passing regenerated catalyst back to the hydroprocessing unit without rejuvenating the spent catalyst.