Systems and methods are provided for slurry hydroconversion of a heavy oil feed, such as an atmospheric or vacuum resid. The systems and methods allow for slurry hydroconversion using catalysts with enhanced activity and/or catalysts that can be recycled as a side product from a complementary refinery process.

Systems and methods are provided for slurry hydroconversion of a heavy oil feed, such as an atmospheric or vacuum resid. The systems and methods allow for slurry hydroconversion using catalysts with enhanced activity and/or catalysts that can be recycled as a side product from a complementary refinery process.

A hydroprocessing catalyst has been developed. The catalyst is a unique transition metal molybdotungsten oxy-hydroxide material. The hydroprocessing using the transition metal molybdotungsten oxy-hydroxide material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A hydroprocessing catalyst has been developed. The catalyst is a unique transition metal molybdotungsten oxy-hydroxide material. The hydroprocessing using the transition metal molybdotungsten oxy-hydroxide material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A process for upgrading pyrolysis tar to higher value products. More particularly, this invention relates to the upgrading of steam cracker tar using relatively small amounts of a transition metal sulfide-containing particulate catalyst dispersed throughout the tar chargestock and in the presence of hydrogen, at relatively mild hydroconversion conditions.

A process for upgrading pyrolysis tar to higher value products. More particularly, this invention relates to the upgrading of steam cracker tar using relatively small amounts of a transition metal sulfide-containing particulate catalyst dispersed throughout the tar chargestock and in the presence of hydrogen, at relatively mild hydroconversion conditions.

Process for converting a heavy hydrocarbon feedstock with initial boiling point of at least 300 C. comprising: a) hydroconverting at least part of said feedstock; b) separating the effluent from stage a) to obtain light and heavy liquid fractions; c) at least two stages of deasphalting in series at least part of the heavy liquid fraction originating from stage b), allowing to separate at least one fraction of asphalt, at least one fraction of heavy deasphalted oil (heavy DAO) and at least one fraction of light deasphalted oil (light DAO), at least one deasphalting stage being carried out using a mixture of at least one polar solvent and at least one apolar solvent, said deasphalting stages being under subcritical conditions of the mixture of solvents; d) recycling at least part of said heavy deasphalted oil cut from stage c) upstream of hydroconverting a) and/or of the inlet of separating b).

Process for converting a heavy hydrocarbon feedstock with initial boiling point of at least 300 C. comprising: a) hydroconverting at least part of said feedstock; b) separating the effluent from stage a) to obtain light and heavy liquid fractions; c) at least two stages of deasphalting in series at least part of the heavy liquid fraction originating from stage b), allowing to separate at least one fraction of asphalt, at least one fraction of heavy deasphalted oil (heavy DAO) and at least one fraction of light deasphalted oil (light DAO), at least one deasphalting stage being carried out using a mixture of at least one polar solvent and at least one apolar solvent, said deasphalting stages being under subcritical conditions of the mixture of solvents; d) recycling at least part of said heavy deasphalted oil cut from stage c) upstream of hydroconverting a) and/or of the inlet of separating b).

Provided herein are compositions and methods for use of an organosilica material comprising a copolymer of at least one monomer of Formula [R.sup.1R.sup.2SiCH.sub.2].sub.3 (I), wherein, R.sup.1 represents a C.sub.1-C.sub.4 alkoxy group; and R.sup.2 is a C.sub.1-C.sub.4 alkoxy group or a C.sub.1-C.sub.4 alkyl group; and at least one other monomer of Formula [(Z.sup.1O).sub.xZ.sup.2.sub.3-xSiZ.sup.3SZ.sup.4] (II), wherein, Z.sup.1 represents a hydrolysable functional group; Z.sup.2 represents a C.sub.1-C.sub.10 alkyl or aryl group; Z.sup.3 represents a C.sub.2-C.sub.11 cyclic or linear hydrocarbon; Z.sup.4 is either H or O.sub.3H; and x represents any one of integers 1, 2, and 3. The composition may be used as a support material to covalently attach transition metal cations, as a sorbent for olefin/paraffin separations, as a catalyst support for hydrogenation reactions, as a precursor for highly dispersed metal nanoparticles, or as a polar sorbent for crude feeds.

The invention relates to a process for preparing bulk metal oxide particles comprising the steps of combining in a reaction mixture (i) dispersible nanoparticles having a dimension of less than about 1 m upon being dispersed in a liquid, (ii) at least one Group VIII non-noble metal compound, (iii) at least one Group VIB metal compound, and (iv) a protic liquid; and reacting the at least one Group VIII non-noble metal compound and the at least one Group VIB metal in the presence of the nanoparticles. It also relates to bulk metal hydroprocessing catalysts obtainable by such method.