The invention relates to a catalytic cracking gasoline upgrading method. First, in the presence of a prehydrogenation catalyst, the full-range FCC gasoline undergoes prehydrogenation in a prehydrogenation reactor to remove diolefins, mercaptans and sulfides, and then the prehydrogenation product undergoes selective hydrodesulfurization in the presence of a hydrodesulfurization-isomerization catalyst, and straight-chain olefins are isomerized into single-branched olefins or single-branched alkanes, thus obtaining a low-olefin, ultralow-sulfur and high-octane clean gasoline product.

Disclosed is a hydrofining catalyst comprising: an inorganic refractory component comprising a first hydrodesulfurization catalytically active component in a mixture with at least one oxide selected from the group consisting of alumina, silica, magnesia, calcium oxide, zirconia and titania; a second hydrodesulfurization catalytically active component; and an organic component comprising a carboxylic acid and optionally an alcohol. The hydrofining catalyst of the present application shows improved performance in the hydrofining of distillate oils. Also disclosed are a hydrofining catalyst system comprising the hydrofining catalyst, a method for preparing the catalyst and catalyst system, and a process for the hydrofining of distillate oils using the catalyst or catalyst system.

A highly active trimetallic mixed transition metal oxide material has been developed. The material may be sulfided to generate metal sulfides which are used as a catalyst in a conversion process such as hydroprocessing. The hydroprocessing may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

According to this invention, a Ni—Mo—W trimetallic catalyst supported on porous alumina is obtained that shows very high activity for hydrotreating (HDT) of gasoils, particularly deep hydrodesulfurization (HDS) and hydrodesnitrogenation (HDN) of straight run gasoil in conditions of moderate pressure. When the catalyst is applied to HDT of diesel, the NiMoW catalyst exhibits high catalytic activity. The content of sulfur and nitrogen in the resulting diesel can be reduced from 13,200 to 10 ppm and nitrogen from 360 ppm to less than 1 ppm, under moderate pressure, temperature and space-velocity (LHSV) similar to those of an industrial unit. The catalytic composition, of trimetallic type, is prepared from an alumina support of high surface area to which a solution containing a metal precursor of an element of group VIB is added, followed by other solution that contains one of the precursors of the active metallic phase, a solution containing another of the precursors of the active metallic phase from group VIB, a metal promoter of group VIII and an additive promoter of acidity from group VB, and finally another solution containing a metal of group VIB, a metal of Group VIII and an organic compound, the used route promotes the preferential formation of well dispersed structures of the used metals on the support of porous alumina, less refractory to sulfidation, with high stacking and short lengths of metal sulfides formed in the resulting hydrodesulfurization catalyst. In the formulation, at least a percentage, but not all the Mo is replaced by W, in a Mo/W molar ratio of 0.6 to 2.0.

The present invention relates to a catalyst and a method for preparation of that catalyst for the selective hydrogenation of diolefins present in gasoline streams along with the shifting of lighter sulfur compounds in the feed stock to heavier sulfur compound by the reaction with olefinic compounds.

A hydroprocessing catalyst or catalyst precursor has been developed. The catalyst is a poorly crystalline transition metal molybdotungstate material or a metal sulfide decomposition product thereof. The hydroprocessing using the crystalline ammonia transition metal molybdotungstate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A catalyst system has been designed that disrupts the sedimentation process. The catalyst system achieves this by saturating key feed components before the feed components are stripped into their incompatible aromatic cores. The efficacy of this disruptive catalyst system is particularly evident in a hydrocracker configuration that runs in two-stage-recycle operation. The catalyst is a self-supported multi-metallic catalyst prepared from a precursor in the hydroxide form, and the catalyst must be toward the top level of the second stage of the two-stage system.

Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.

The present invention clarifies the characteristic of the hygroscopicity of the catalyst for producing acrylic acid and finds out a relationship between the water amount of the catalyst and the catalytic performance as the catalyst for producing acrylic acid, and provides an excellent catalyst. Provided is a catalyst for producing acrylic acid, which contains molybdenum and vanadium as essential active components, in which the amount of water contained in the catalyst is 0.01 mass % or more and 0.53 mass % or less.

A highly active quaternary mixed transition metal oxide material has been developed. The material may be sulfided to generate metal sulfides which are used as a catalyst in a conversion process such as hydroprocessing. The hydroprocessing may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.