A method for producing a multimetal oxide catalyst comprises preparation of a precursor composition, exposing said precursor composition to elevated temperatures to activate the composition, and grinding the activated composition. The preparation of the precursor composition comprises: a) forming a plasticized precursor composition from the constituents of the composition; b) discharging the plasticized precursor composition from an extruder having at least one die to form extrudates; c) allowing the extrudates to drop onto a transfer surface disposed beneath the at least one die whereby the extrudates break into pieces which come to rest on the transfer surface; d) transferring the pieces to at least one drying chamber; and e) moving the pieces, through the at least one drying chamber on an air permeable drying conveyor belt; wherein steps b) through d) are carried out under reduced pressure. The method allows the production of a multimetal oxide catalyst with uniform characteristics. Fine particles of the multimetal oxide precursor that may be generated during extrusion of the plasticized precursor composition and handling of the extrudates are removed.

Processes for transforming an inert metal component into an active metal catalyst are provided. Apparatus and methods using active metal catalyst prepared according the process described herein are also provided.

A catalyst comprising a carrier and a metals component impregnated in the carrier, the carrier comprising alumina; and the metals component comprising a first metals fraction and a second metals fraction, the first metals fraction comprising at least one metal selected from chromium, molybdenum, or tungsten, and the second metals fraction comprising at least two metals selected from cobalt, rhodium, iridium, nickel, palladium, or platinum, wherein the catalyst has a first pore volume of 0.28 to 0.45 mL/g for pores having a pore diameter of 12 nm to less than 16 nm, and a second pore volume of 0.15 to 0.28 mL/g for pores of 2.0 nm to less than 12.0 nm.

The present invention is in the field of heterogeneous catalysis. Particularly, the present invention relates to a process for preparing catalysts advantageously usable in the hydrotreatment processes, for example in hydrodesulphurization, hydrodenitrogenation, hydrodearomatization processes of hydrocarbons. More in particular, the present invention relates to a process for obtaining said catalysts, which comprise mixed oxides of Nickel, Aluminum, Molybdenum and Tungsten and optionally a transition metal Me selected from the group consisting of Zn, Mn, Cd, and a mixture thereof, an organic component C, and possibly an inorganic binder B. Said mixed oxides comprise an amorphous phase and a pseudo-crystalline phase isostructural to Wolframite. The present invention further relates to said hydrotreatment catalysts and a hydrotreatment process wherein said catalysts are used.

Provided is a refining apparatus of a waste plastic pyrolysis oil including a reactor where a waste plastic pyrolysis oil is introduced and hydrotreated, wherein the reactor includes Area 1 including a hydrotreating catalyst having a Mo content of 1 to 15 wt % with respect to the total weight; and Area 2 including a hydrotreating catalyst having a Mo content of 5 to 40 wt % and a Ni or Co content of 4 to 50 wt % with respect to the total weight, and the waste plastic pyrolysis oil is refined by passing through Area 1 and Area 2 sequentially.

The invention concerns a method for rejuvenating an at least partially used catalyst originating from a hydroprocessing and/or hydrocracking process, the at least partially used catalyst being derived from a fresh catalyst comprising at least one group VIII metal (in particular, Co), at least one group VIB metal (in particular, Mo), an oxide support, and optionally phosphorus, the method comprising the steps: ⋅a) regenerating the at least partially used catalyst in a gas stream containing oxygen at a temperature between 300° C. and 550° C. so as to obtain a regenerated catalyst, ⋅b) then placing the regenerated catalyst in contact with phosphoric acid and an organic acid, each having acidity constant pKa greater than 1.5, ⋅c) performing a drying step at a temperature less than 200° C. without subsequently calcining it, so as to obtain a rejuvenated catalyst.

Bulk catalysts comprised of nickel, molybdenum, tungsten and titanium and methods for synthesizing bulk catalysts are provided. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

The present application relates to a hydrogenation catalyst, a process for producing the same and application thereof in the hydrotreatment of feedstock oil. The process comprises at least the following steps: (1) contacting a first active metal component and a first organic complexing agent with a carrier to obtain a composite carrier; (2) calcining the composite carrier to obtain a calcined composite carrier having a total carbon content of 1% by weight or less; and (3) contacting a second organic complexing agent with the calcined composite carrier to obtain the hydrogenation catalyst. The hydrogenation catalyst has both excellent hydrodesulfurization activity and hydrodenitrogenation activity, and exhibits a significantly prolonged service life.

Provided is a novel catalyst comprised of an alumina, silica-alumina, and a zeolite containing base impregnated with Ni, Mo, and W. In one embodiment, the trimetallic catalyst is layered with a conventional hydrocracking pretreat catalyst to provide a catalyst combination useful in hydrotreating a feed to a hydrocracking stage.

A subject matter of the invention is a catalyst comprising a support and an active phase consisting of nickel, molybdenum and tungsten, and phosphorus, the nickel content, measured in the NiO form, is between 3% and 4% by weight; the molybdenum content, measured in the MoO.sub.3 form, is between 2% and 4% by weight; the tungsten content, measured in the WO.sub.3 form, is between 34% and 40% by weight; the phosphorus content, measured in the P.sub.2O.sub.5 form, is between 3% and 4% by weight, with respect to the total weight of the catalyst; the WO.sub.3/MoO.sub.3 molar ratio is between 5.3 and 12.4 mol/mol, the NiO/(WO.sub.3 + MoO.sub.3) molar ratio is between 0.20 and 0.33 mol/mol and the P.sub.2O.sub.5/(WO.sub.3 + MoO.sub.3) molar ratio is between 0.21 and 0.34 mol/mol. The invention also relates to its method of preparation and to its use in hydrotreating and/or hydrocracking.