This invention disclosure reported here a supported metal hydroxide adsorbent and a method for its preparation as well as a method for its oxidative regeneration. The supported metal hydroxide adsorbent comprises metal hydroxide and support with a mass ratio of 5-30:100. The adsorbent disclosed in present invention exhibited outstanding adsorption capacity and high selectivity to sulfur impurity in gasoline. The method of oxidative regeneration provides an efficient way for the recovery of the saturated adsorbent.

This invention disclosure reported here a supported metal hydroxide adsorbent and a method for its preparation as well as a method for its oxidative regeneration. The supported metal hydroxide adsorbent comprises metal hydroxide and support with a mass ratio of 5-30:100. The adsorbent disclosed in present invention exhibited outstanding adsorption capacity and high selectivity to sulfur impurity in gasoline. The method of oxidative regeneration provides an efficient way for the recovery of the saturated adsorbent.

Processes for upgrading a hydrocarbon. In some embodiments, the process can include contacting a hydrocarbon-containing feed with a first catalyst that can include a Group 8-10 element disposed on a support within a first conversion zone to effect dehydrogenation, dehydroaromatization, and/or dehydrocyclization of a portion of the feed to produce first conversion zone effluent that includes one or more upgraded hydrocarbons, molecular hydrogen, and unconverted feed. The process can also include contacting the first conversion zone effluent with a second catalyst that can include a Group 8-10 element disposed on a support within a second conversion zone to effect dehydrogenation, dehydroaromatization, and/or dehydrocyclization of at least a portion of the unconverted feed to produce a second conversion zone effluent that includes an additional quantity of upgraded hydrocarbon(s) and molecular hydrogen. A temperature of the second conversion zone effluent can be greater than a temperature of the first conversion zone effluent.

An adsorbent composition for removing chlorides from hydrocarbon includes an adsorbent matrix and a metallic component. The metallic component forms an intimate complex with the adsorbent matrix. The adsorbent composition is characterized by pore size in the range of 20 Å to 120 Å. It is found that the amount of chlorides removed by the adsorbent composition from the hydrocarbon is in the range of 0.020 wt. % to 0.047 wt. %.

A reversible enrichment material, its preparation and application thereof are provided. The reversible enrichment material includes an inorganic carrier; and an active metal salt, a first metal salt promoter and a second metal salt promoter supported on the inorganic carrier. The active metal salt is a soluble silver salt, a soluble copper salt, or a combination thereof. The first metal salt promoter is one or more selected from the group consisting of soluble salts of Group IA, Group IIA and Group IIIA metals, and the second metal salt promoter is one or more selected from the group consisting of soluble salts of transition metals other than Group IB metals. The reversible enrichment material can realize effective separation of saturated hydrocarbon from unsaturated hydrocarbon and has good reversibility.

A reversible enrichment material, its preparation and application thereof are provided. The reversible enrichment material includes an inorganic carrier; and an active metal salt, a first metal salt promoter and a second metal salt promoter supported on the inorganic carrier. The active metal salt is a soluble silver salt, a soluble copper salt, or a combination thereof. The first metal salt promoter is one or more selected from the group consisting of soluble salts of Group IA, Group IIA and Group IIIA metals, and the second metal salt promoter is one or more selected from the group consisting of soluble salts of transition metals other than Group IB metals. The reversible enrichment material can realize effective separation of saturated hydrocarbon from unsaturated hydrocarbon and has good reversibility.

A process for producing olefins from the hydrocarbon feed includes introducing the hydrocarbon feed into a Solvent Deasphalting Unit (SDA) to remove asphaltene from the hydrocarbon feed producing a deasphalted oil stream, wherein the SDA comprises a solvent that reacts with the hydrocarbon feed, and the deasphalted oil stream comprises from 0.01 weight percent (wt. %) to 18 wt. % asphaltenes; introducing the deasphalted oil stream into a steam catalytic cracking system; steam catalytically cracking the deasphalted oil stream in the steam catalytic cracking system in the presence of steam and a nano zeolite cracking catalyst to produce a steam catalytic cracking effluent; and separating the olefins from the steam catalytic cracking effluent.

A process for producing olefins from the hydrocarbon feed includes introducing the hydrocarbon feed into a Solvent Deasphalting Unit (SDA) to remove asphaltene from the hydrocarbon feed producing a deasphalted oil stream, wherein the SDA comprises a solvent that reacts with the hydrocarbon feed, and the deasphalted oil stream comprises from 0.01 weight percent (wt. %) to 18 wt. % asphaltenes; introducing the deasphalted oil stream into a steam catalytic cracking system; steam catalytically cracking the deasphalted oil stream in the steam catalytic cracking system in the presence of steam and a nano zeolite cracking catalyst to produce a steam catalytic cracking effluent; and separating the olefins from the steam catalytic cracking effluent.

A process for upgrading a hydrocarbon feed, such as crude oil or other heavy oils, may include hydrotreating a hydrocarbon feed in a hydrotreating unit to produce a hydrotreated effluent that includes asphaltenes, coke precursors, or both. The process further includes hydrocracking the hydrotreated effluent in a hydrocracking unit to produce a hydrocracked effluent, adsorbing at least a portion of the asphaltenes, coke precursors, or both, from the hydrotreated effluent, the hydrocracked effluent, or both, separating the hydrocracked effluent into at least an upgraded lesser-boiling effluent and a greater-boiling effluent in a hydrocracked effluent separation system, and steam cracking the upgraded lesser-boiling effluent to produce olefins, aromatic compounds, or combinations of these. The process may further include recycling the greater boiling effluent back to the hydrotreating unit and hydrocracking a middle distillate effluent from the hydrocracked effluent separation system. Systems for conducting the processes are also disclosed.

A process for treating a hydrocarbon stream to remove polynuclear aromatic (PNA) and heavy polynuclear aromatic (HPNA) compounds includes contacting the hydrocarbon stream with an adsorbent in an adsorption unit to adsorb the PNA and HPNA compounds onto the adsorbent to produce a treated hydrocarbon stream and regenerating the adsorbent. Regenerating the adsorbent may include contacting the adsorbent with a solvent comprising a disulfide oil, such as a disulfide oil effluent from a mercaptan oxidation unit. The solvent comprising the disulfide oil desorbs the PNA and HPNA compounds from the adsorbent into the solvent to produce a desorption effluent. The treated hydrocarbon stream can be passed to a hydrocracking unit that hydrocracks the treated hydrocarbon stream to produce a hydrocracker effluent that includes greater value petrochemical products or intermediates.