Abstract: A catalyst is provided for hydrodeoxygenation and hydroisomerization of paraffins having higher activity. The catalyst contains a molecular sieve, such as SAPO-11, a metal component such as platinum and/or palladium or nickel tungsten sulfide or nickel molybdenum sulfide and a binder such as gamma alumina. The catalyst exhibits a high proportion of weak acid sites and a relatively equal distribution of the metal component on the molecular sieve and the binder.

Abstract: A catalyst is provided for hydrodeoxygenation and hydroisomerization of paraffins having higher activity. The catalyst contains a molecular sieve, such as SAPO-11, a metal component such as platinum and/or palladium or nickel tungsten sulfide or nickel molybdenum sulfide and a binder such as gamma alumina. The catalyst exhibits a high proportion of weak acid sites and a relatively equal distribution of the metal component on the molecular sieve and the binder.

Abstract: A catalyst is provided for hydrodeoxygenation and hydroisomerization of paraffins having higher activity. The catalyst contains a molecular sieve, such as SAPO-11, a metal component such as platinum and/or palladium or nickel tungsten sulfide or nickel molybdenum sulfide and a binder such as gamma alumina. The catalyst exhibits a high proportion of weak acid sites and a relatively equal distribution of the metal component on the molecular sieve and the binder.

Abstract: A catalyst is provided for hydrodeoxygenation and hydroisomerization of paraffins having higher activity. The catalyst contains a molecular sieve, such as SAPO-11, a metal component such as platinum and/or palladium or nickel tungsten sulfide or nickel molybdenum sulfide and a binder such as gamma alumina. The catalyst exhibits a high proportion of weak acid sites and a relatively equal distribution of the metal component on the molecular sieve and the binder.

Abstract: Catalysts are described. The catalysts comprise a dried extrudate of a mixture of ?-alumina and at least one mixed metal oxide or mixed metal hydroxide, the ?-alumina having a BET surface area of 150 m2/g to 275 m2/g. Processes of making the hydroprocessing catalysts, and hydroprocessing processes using the catalysts are also described.

Abstract: The present invention discloses a process and apparatus for selectively hydrogenating diolefins in a cracked stream. The method combines a conversion unit and a recovery section. The recovery section includes the diolefin hydrogenation reactor that is used to selectively hydrogenate the diolefins in the cracked naphtha. The diolefin depleted naphtha may be debutanized to separate the stabilized naphtha and liquefied petroleum gas streams.

Abstract: A process and apparatus for reducing the sulfur content of naphtha. The process includes introducing at least a portion of a naphtha feed stream to a selective hydrodesulfurization zone under selective hydrodesulfurization conditions in the presence of a selective hydrodesulfurization catalyst to form a low sulfur stream which contains mercaptan and thiophene compounds. At least a portion of the low sulfur stream is separated into at least two streams, a mercaptan rich stream containing mercaptan and thiophene compounds and an overhead stream containing hydrogen sulfide and liquid petroleum gas. The mercaptan rich stream is treated in an adsorbent zone to remove at least a portion of the mercaptan and thiophene compounds to form a mercaptan lean stream.

Abstract: Methods and apparatuses are disclosed for upgrading a hydrocarbon feedstream comprising passing the hydrocarbon feedstream to a first hydroprocessing reactor in a reaction vessel to produce a first hydroprocessed effluent stream. The first hydroprocessed effluent stream is separated in a hot separator to produce a vapor stream and a liquid hydrocarbon stream. At least a portion of the liquid hydrocarbon stream is passed to a second hydroprocessing reactor disposed in the reaction vessel above the first hydroprocessing reactor, to produce a second hydroprocessed effluent stream. A liquid product stream is separated from the second hydroprocessing effluent stream. The vapor stream from the hot separator is mixed with the liquid product stream to provide a combined stream.

Abstract: A process for reducing the sulfur content of FCC naphtha is described. The process includes introducing a FCC naphtha feed to a selective hydrogenation zone to form a hydrogenated feed. The hydrogenated feed is separated into light fraction and a heavy fraction. The heavy fraction is introduced into a selective hydrodesulfurization zone to form a desulfurized stream which contains mercaptans. The desulfurized stream is separated into a mercaptan rich stream and a mercaptan lean stream. The mercaptan rich stream is treated with a caustic extraction process, a hydrodesulfurization reaction zone, a selective hydrogenation process, an adsorption process, or an ionic liquid extraction process to remove at least a portion of the mercaptan compounds to form a second mercaptan lean stream.

Abstract: A process and apparatus for reducing the sulfur content of naphtha. The process includes introducing at least a portion of a naphtha feed stream to a selective hydrodesulfurization zone under selective hydrodesulfurization conditions in the presence of a selective hydrodesulfurization catalyst to form a low sulfur stream which contains mercaptan and thiophene compounds. At least a portion of the low sulfur stream is separated into at least two streams, a mercaptan rich stream containing mercaptan and thiophene compounds and an overhead stream containing hydrogen sulfide and liquid petroleum gas. The mercaptan rich stream is treated in an adsorbent zone to remove at least a portion of the mercaptan and thiophene compounds to form a mercaptan lean stream.

Abstract: The present invention discloses a process and apparatus for selectively hydrogenating diolefins in a cracked stream. The method combines a conversion unit and a recovery section. The recovery section includes the diolefin hydrogenation reactor that is used to selectively hydrogenate the diolefins in the cracked naphtha. The diolefin depleted naphtha may be debutanized to separate the stabilized naphtha and liquefied petroleum gas streams.

Abstract: Methods and apparatus for removing sulfur compounds from a hydrocarbon stream are disclosed. In one exemplary embodiment, a method for removing sulfur compounds from a hydrocarbon stream includes the steps of steam stripping a mixed hydrocarbon stream to form a steam stripped overhead stream comprising naphtha and lighter hydrocarbons and a steam stripped bottoms stream comprising naphtha and heavier hydrocarbons; fractionating the steam stripped bottoms stream to form a fractionated overhead stream comprising naphtha hydrocarbons; combining the steam stripped overhead stream with a portion of the fractionated overhead stream and an H2-rich makeup gas stream; and hydrodesulfurizing the combined stream to form an HDS reaction effluent stream.

Abstract: The process and apparatus of the present invention selectively hydrogenates a heavier olefinic naphtha stream in an upstream catalyst bed and the hydrogenated effluent and a lighter olefinic naphtha stream in a downstream catalyst bed. The heavier di-alkenes are less re-active and are contacted with more hydrogenation catalyst than the lighter di-alkenes which are more re-active.

Abstract: Methods and apparatuses for processing hydrocarbon streams containing organic nitrogen species are provided. In an embodiment, a method for processing a hydrocarbon stream containing organic nitrogen species includes adding an aqueous acidic solution to a hydrocarbon feed stream to form a reaction stream. The method further includes contacting the reaction stream with a reaction surface and reacting the aqueous acidic solution and the organic nitrogen species to form an ammonium sulfate rich stream and a lean nitrogen naphtha stream. Also, the method includes separating an ammonium sulfate rich aqueous phase and an oil phase from the ammonium sulfate rich stream.

Abstract: A method and apparatus for processing hydrocarbons are described. The method includes fractionating a hydrocarbon stream to form at least two fractions. The first fraction is reformed to form a reformate stream, and the reformate stream is introduced into an aromatics processing zone to produce aromatic products. At least a portion of the second fraction is cracked in a fluid catalytic cracking unit. A selectively hydrogenated light naphtha stream is formed by separating the cracked hydrocarbon stream into at least two streams and selectively hydrogenating the light naphtha stream, or selectively hydrogenating the cracked hydrocarbon stream and separating the hydrogenated cracked hydrocarbon stream into at least two streams. Aromatics are extracted from the selectively hydrogenated light naphtha stream forming an extract stream and a raffinate stream. The extract stream is hydrotreated, sent to the aromatics processing zone to produce additional aromatic products.

Abstract: Methods and apparatuses for desulfurizing hydrocarbon streams are provided herein. In one embodiment, a method for desulfurizing a hydrocarbon stream includes separating the hydrocarbon stream into a heavier fraction and a lighter fraction. The heavier fraction includes a relatively higher amount of lower octane mono-unsaturates and the lighter fraction includes a relatively higher amount of higher octane mono-unsaturates. The method further includes hydrodesulfurizing the heavier fraction in a first hydrodesulfurization zone and hydrodesulfurizing the lighter fraction in a second hydrodesulfurization zone. Further, the method forms a hydrodesulfurized stream from the heavier fraction and the lighter fraction.

Abstract: The process and apparatus of the present invention selectively hydrogenates a heavier olefinic naphtha stream in an upstream catalyst bed and the hydrogenated effluent and a lighter olefinic naphtha stream in a downstream catalyst bed. The heavier di-alkenes are less re-active and are contacted with more hydrogenation catalyst than the lighter di-alkenes which are more re-active.

Abstract: A process for removing sulfur and nitrogen contaminants from a hydrocarbon stream using a Brønsted acid or an ionic liquid and a Brønsted acid is described. The process includes contacting the hydrocarbon stream comprising the contaminant with a Brønsted acid or a hydrocarbon-immiscible ionic liquid and the Brønsted acid to produce a mixture comprising the hydrocarbon and the Brønsted acid comprising at least a portion of the removed contaminant or a hydrocarbon-immiscible ionic liquid comprising at least a portion of the removed contaminant; and separating the mixture to produce a hydrocarbon effluent having a reduced level of the contaminant and a Brønsted acid effluent comprising the Brønsted acid comprising at least the portion of the removed contaminant or a hydrocarbon-immiscible ionic liquid effluent comprising the hydrocarbon-immiscible ionic liquid comprising at least the portion of the removed contaminant.

Abstract: The process and apparatus of the present invention selectively hydrogenates a heavier olefinic naphtha stream in an upstream catalyst bed and the hydrogenated effluent and a lighter olefinic naphtha stream in a downstream catalyst bed. The heavier di-alkenes are less re-active and are contacted with more hydrogenation catalyst than the lighter di-alkenes which are more re-active.

Abstract: The process and apparatus of the present invention selectively hydrogenates a heavier olefinic naphtha stream in an upstream catalyst bed and the hydrogenated effluent and a lighter olefinic naphtha stream in a downstream catalyst bed. The heavier di-alkenes are less re-active and are contacted with more hydrogenation catalyst than the lighter di-alkenes which are more re-active.