A process for reducing the benzene content of a light reformate refinery stream comprises the following steps: a) reducing the benzene content by exposing the light reformate to hydrogenation conditions in a benzene-saturation reactor bed, b) increasing the octane number of the hydrogenated light reformate produced in step a) by exposing it to isomerization conditions, c) further reducing the benzene content by exposing the light reformate refinery stream to further hydrogenation conditions, wherein the isomerization of step b) occurs after step a), the hydrogenation of step c) does not precede the isomerization step b), and steps a), b) and c) are all carried out within the same reactor.

A process for reducing the benzene content of a light reformate refinery stream comprises the following steps: a) reducing the benzene content by exposing the light reformate to hydrogenation conditions in a benzene-saturation reactor bed, b) increasing the octane number of the hydrogenated light reformate produced in step a) by exposing it to isomerization conditions, c) further reducing the benzene content by exposing the light reformate refinery stream to further hydrogenation conditions, wherein the isomerization of step b) occurs after step a), the hydrogenation of step c) does not precede the isomerization step b), and steps a), b) and c) are all carried out within the same reactor.

In accordance with one or more embodiments of the present disclosure, a method for producing aromatic compounds from pyrolysis gasoline comprising C.sub.5-C.sub.6 non-aromatic hydrocarbons includes aromatizing the pyrolysis gasoline in an aromatization unit, thereby converting the C.sub.5-C.sub.6 non-aromatic hydrocarbons to a first stream comprising benzene-toluene-xylenes (BTX); hydrotreating the first stream comprising BTX in a selective hydrotreatment unit, thereby producing a de-olefinated stream comprising BTX hydrodealkylating and transalkylating the de-olefinated stream comprising BTX in a hydrodealkylation-transalkylation unit, thereby producing a second stream comprising BTX, the second stream comprising BTX having a greater amount of benzene and xylenes than the first stream comprising BTX; and processing the second stream comprising BTX in an aromatics recovery complex, thereby producing the aromatic compounds from the pyrolysis gasoline, the aromatic compounds comprising benzene, toluene, and xylenes.

In accordance with one or more embodiments of the present disclosure, a method for producing aromatic compounds from pyrolysis gasoline comprising C.sub.5-C.sub.6 non-aromatic hydrocarbons includes aromatizing the pyrolysis gasoline in an aromatization unit, thereby converting the C.sub.5-C.sub.6 non-aromatic hydrocarbons to a first stream comprising benzene-toluene-xylenes (BTX); hydrotreating the first stream comprising BTX in a selective hydrotreatment unit, thereby producing a de-olefinated stream comprising BTX; hydrodealkylating and transalkylating the de-olefinated stream comprising BTX in a hydrodealkylation-transalkylation unit, thereby producing a second stream comprising BTX, the second stream comprising BTX having a greater amount of benzene and xylenes than the first stream comprising BTX; and processing the second stream comprising BTX in an aromatics recovery complex, thereby producing the aromatic compounds from the pyrolysis gasoline, the aromatic compounds comprising benzene, toluene, and xylenes.

A catalyst may include a metallic function derived from a metal constrained within cages and/or channels of a microporous material, wherein the cages and/or channels of the microporous material are defined by 8 tetrahedral atoms or fewer; and an acidic function derived from an additional zeolite having cages and/or channels defined by 10 or more tetrahedral atoms, wherein the microporous material providing the metallic function and additional zeolite providing the acidic function are coupled by a binder.

A catalyst may include a metallic function derived from a metal constrained within cages and/or channels of a microporous material, wherein the cages and/or channels of the microporous material are defined by 8 tetrahedral atoms or fewer; and an acidic function derived from an additional zeolite having cages and/or channels defined by 10 or more tetrahedral atoms, wherein the microporous material providing the metallic function and additional zeolite providing the acidic function are coupled by a binder.

Catalysts including at least one microporous material (e.g., zeolite), an organosilica material binder, and at least one catalyst metal are provided herein. Methods of making the catalysts, preferably without surfactants and processes of using the catalysts, e.g., for aromatic hydrogenation, are also provided herein.

Catalysts including at least one microporous material (e.g., zeolite), an organosilica material binder, and at least one catalyst metal are provided herein. Methods of making the catalysts, preferably without surfactants and processes of using the catalysts, e.g., for aromatic hydrogenation, are also provided herein.

The invention relates to a hydrocarbon hydroprocessing catalyst comprising a support based on at least one refractory oxide, at least one metal from group VIII and at least one metal from group VIB. The inventive catalyst is characterized in that it also comprises at least one organic compound having formula (I) or (II): ##STR00001##
in which each R.sub.1 represents independently an alkyl group at C.sub.1-18, an alkenyl group at C.sub.2-18, an aryl group at C.sub.6-18, a cycloalkyl group at C.sub.3-8, an alkylaryl or arylalkyl group at C.sub.7-20, or the two R.sub.1 groups together form a divalent group at C.sub.2-18, and R.sub.2 represents an alkylene group at C.sub.1-18, an arylene group at C.sub.6-18, a cycloalkylene group at C.sub.3-7, or a combination of same. The invention also relates to a method of preparing one such catalyst and to the use thereof for hydroprocessing or hydrocracking.

A method of producing a regenerated hydrotreating catalyst, including a first step of preparing a hydrotreating catalyst that has been used for hydrotreatment of a petroleum fraction and has a metal element selected from Group 6 elements of the periodic table; a second step of performing regeneration treatment for part of the catalyst prepared in the first step, then performing X-ray absorption fine structure analysis for the catalyst after the regeneration treatment, and obtaining regeneration treatment conditions in which a ratio IS/IO of a peak intensity IS of a peak attributed to a bond between the metal element and a sulfur atom to a peak intensity IO of a peak attributed to a bond between the metal element and an oxygen atom is in the range of 0.1 to 0.3 in a radial distribution curve obtained from an extended X-ray absorption fine structure spectrum.