A single-pot method of producing a hydrodesulfurization catalyst by hydrothermally treating a hydrothermal precursor that includes a silica source, a structural directing surfactant, an aqueous acid solution, and metal precursors that contain active catalyst materials is provided. The hydrodesulfurization catalyst includes a catalyst support having SBA-15 and preferably titanium, wherein the active catalyst materials are homogenously deposited on the catalyst support. Various embodiments of said method and the hydrodesulfurization catalyst are also provided.

A process for hydrodesulfurizing an olefinic naphtha feedstock while retaining a substantial amount of the olefins, which feedstock has a T95 boiling point below 250 C. boils and contains at least 50 ppmw of organically bound sulfur and from 5% to 60% olefins, said process including (a) selective diolefin hydrogenation, under reaction conditions to convert at least 50% or 90% of the diolefins to paraffins or mono-olefins providing a pre-treated feedstock, (b) hydrodesulfurizing the pre-treated feedstock in a sulfur removal stage in the presence of hydrogen and a hydrodesulfurization catalyst, at hydrodesulfurization reaction conditions to convert at least 50% of the organically bound sulfur to hydrogen sulfide and to produce a desulfurized product stream containing from 0 ppmw to 50 ppmw organically bound sulfur, with the associated benefit of such a process providing a lower octane loss, compared to a process with a lower gas to oil ratio.

The invention provides a process for preparing a fluid having a boiling point in the range of from 150 to 260 C. and comprising more than 80% by weight of isoparaffins and less than 50 ppm of aromatics, comprising the step of catalytically hydrogenating a feed comprising more than 85% by weight of oligomerized olefins, at a temperature from 115 to 195 C. and at a pressure from 30 to 70 bars. The invention also provides the fluid obtainable by the process of the invention and the use of said fluid.

The invention provides a process for preparing a fluid having a boiling point in the range of from 150 to 260 C. and comprising more than 80% by weight of isoparaffins and less than 50 ppm of aromatics, comprising the step of catalytically hydrogenating a feed comprising more than 85% by weight of oligomerized olefins, at a temperature from 115 to 195 C. and at a pressure from 30 to 70 bars. The invention also provides the fluid obtainable by the process of the invention and the use of said fluid.

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.

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.

The present invention belongs to the field of petrochemical industry, and discloses a method for selective hydrogenation of butadiene extraction tail gas and a selective hydrogenation apparatus thereof. The method for selective hydrogenation of butadiene extraction tail gas comprises: (1) an alkyne-containing tail gas from a butadiene extraction unit is fed into a raw material tank, optionally impurities entrained in the alkyne-containing tail gas are removed before being fed into the raw material tank; (2) a C4 raw material in the raw material tank is pressurized by a feed pump to a pressure required for reaction, then merged with a circulated C4 stream from a first-stage reactor outlet buffer tank and fed into a first-stage mixer, wherein it is mixed with hydrogen gas, and fed into the first-stage reactor to undergo a first-stage hydrogenation reaction, and a first-stage reaction stream obtained by the reaction is fed into the first-stage reactor outlet buffer tank; the hydrogen gas required for the reaction in the first-stage reactor is fed through a first feeding mode or a second feeding mode: the first feeding mode comprises: all the hydrogen gas required for the reaction is fed through the first-stage reactor outlet buffer tank, and then fed into the first-stage reactor through a first route at an outlet of the first-stage reactor outlet buffer tank; the second feeding mode comprises: a part of the hydrogen gas required for the reaction is fed through the first-stage reactor outlet buffer tank, and then fed into the first-stage reactor through the first route at an outlet of the first-stage reactor outlet buffer tank; and the other part of the hydrogen gas is fed through the first-stage mixer, and then fed into the first-stage reactor; (3) there is no gas-phase discharge from the first-stage reactor outlet buffer tank, and a liquid-phase product is divided into at least two streams, the first stream is returned to the first-stage reactor as the circulated C4 stream, and the second stream is used as a feed to a stabilization tower or subjected to further hydrotreatment prior to being fed into the stabilization tower; (4) a C4 hydrogenation product is recovered after separation in the stabilization tower.

The present invention belongs to the field of petrochemical industry, and discloses a method for selective hydrogenation of butadiene extraction tail gas and a selective hydrogenation apparatus thereof. The method for selective hydrogenation of butadiene extraction tail gas comprises: (1) an alkyne-containing tail gas from a butadiene extraction unit is fed into a raw material tank, optionally impurities entrained in the alkyne-containing tail gas are removed before being fed into the raw material tank; (2) a C4 raw material in the raw material tank is pressurized by a feed pump to a pressure required for reaction, then merged with a circulated C4 stream from a first-stage reactor outlet buffer tank and fed into a first-stage mixer, wherein it is mixed with hydrogen gas, and fed into the first-stage reactor to undergo a first-stage hydrogenation reaction, and a first-stage reaction stream obtained by the reaction is fed into the first-stage reactor outlet buffer tank; the hydrogen gas required for the reaction in the first-stage reactor is fed through a first feeding mode or a second feeding mode: the first feeding mode comprises: all the hydrogen gas required for the reaction is fed through the first-stage reactor outlet buffer tank, and then fed into the first-stage reactor through a first route at an outlet of the first-stage reactor outlet buffer tank; the second feeding mode comprises: a part of the hydrogen gas required for the reaction is fed through the first-stage reactor outlet buffer tank, and then fed into the first-stage reactor through the first route at an outlet of the first-stage reactor outlet buffer tank; and the other part of the hydrogen gas is fed through the first-stage mixer, and then fed into the first-stage reactor; (3) there is no gas-phase discharge from the first-stage reactor outlet buffer tank, and a liquid-phase product is divided into at least two streams, the first stream is returned to the first-stage reactor as the circulated C4 stream, and the second stream is used as a feed to a stabilization tower or subjected to further hydrotreatment prior to being fed into the stabilization tower; (4) a C4 hydrogenation product is recovered after separation in the stabilization tower.

Systems and methods for producing a wash oil using a light fuel oil (e.g., cracked distillate) are disclosed. The methods include hydrogenating the cracked distillate and separating the hydrogenated cracked distillate to remove C.sub.4 to C.sub.6 hydrocarbons to produce the wash oil.

An integrated process for forming a combined feedstock stream comprising catalytically cracking a first hydrocarbon feedstock to form a full range cracked full naphtha stream and a first light olefins stream, steam cracking a second hydrocarbon feedstock to form a pyrolysis gasoline stream and a second light olefins stream mixing at least a portion of each of the full range cracked naphtha stream and the pyrolysis gasoline stream to form a combined stream, hydro-processing the combined stream to form a hydro-processed combined stream splitting the hydro-processed combined stream into a C.sub.5/C.sub.6 stream, and a first aromatic rich stream, splitting the first aromatic rich stream into a second aromatic rich stream and a heavy oil stream.