Provided is a conversion process for an organic oil, relating to the field of biomass utilization, energy and chemical industry. The conversion process is carried out in presence of an aqueous slurry and a catalyst selected from the group consisting of an iron oxide compound, a waste agent resulting from use of an iron oxide compound as desulfurizer, and a regeneration product of the waste agent, under a controlled molar ratio of iron element to sulfur element. It is found that free radical condensation polymerization of organic oil during cracking process can be blocked effectively by using carbonylation, and hydrogenation is achieved with active hydrogen produced from the conversion of CO and water. In the conversion process, organic material, especially biomass solid, can be directly converted without dehydration, and water can be additionally added to the biomass liquid or the mineral oil.

A process plant and a process for production of a hydrocarbon suitable for use as jet fuel from a feedstock being a renewable feedstock or an oxygenate feedstock, including combining the feedstock with an amount of a liquid diluent, directing it to contact a material catalytically active in hydrodeoxygenation under hydrotreating conditions to provide a hydrodeoxygenated intermediate product, separating the hydrodeoxygenated intermediate product in at least two fractions; a vapor fraction and a liquid fraction, directing at least an amount of the liquid fraction to contact a material catalytically active in isomerization under isomerization conditions to provide an isomerized intermediate product, directing at least an amount of the isomerized intermediate product and a stream comprising sulfur to provide a hydrocracked intermediate product, and fractionating the hydrocracked intermediate product to provide at least a hydrocarbon suitable for use as jet fuel.

Catalysts for the hydrogenation of aromatic containing polymers are described. Such a catalyst can include, based on the total weight of the catalyst, 99.1 wt. % to 99.95 wt. % of a metal oxide support, and 0.05 wt. % to 0.9 wt. % of catalytic metal nanoparticles comprising platinum (Pt), palladium (Pd), ruthenium (Ru), any combination thereof, or alloy thereof. The catalyst can have a specific surface area of 5 m.sup.2/g to 80 m.sup.2/g, a pore volume of 0.01 cm.sup.3/g to 0.35 cm.sup.3/g, and a catalyst median particle size of less than 300 microns. Processes to produce the catalyst and methods of hydrogenating aromatic containing polymers are also described.

The present invention is based on the use of a two-step hydrocracking process for the production of naphtha, comprising a step of hydrogenation placed downstream of the second hydrocracking step, the hydrogenation step treating the effluent resulting from the second hydrocracking step in the presence of a specific hydrogenation catalyst. Furthermore, the hydrogenation step and the second hydrocracking step are performed under specific operating conditions and in particular under quite specific temperature conditions.

A hydrofinishing catalyst according to the present invention includes an amorphous silica-alumina support; and a hydrogenated active metal supported on the support, and has an Al composition having a total mass (wt %) of Al and Si as a denominator and a mass (wt %) of Al as a numerator with respect to a reference line, which is a straight line passing through the center of a cross-section of the support, locations evenly spaced apart along the reference line are sequentially numbered, where composition uniformity, which is defined as UN by the Al composition at the i-th location and an average Al composition at the cross-section of the support passing through the center of the support, is 3.0 or less.

Provided are a full conversion process and a device thereof for producing light aromatic hydrocarbon from LCO. The process includes the steps of: subjecting LCO stream to hydrofining and impurity separation, then performing selective conversion reaction, and separating the mixed aromatic hydrocarbons generated to sequentially separate out light aromatic hydrocarbons such as benzene-toluene and xylene, C.sub.9A aromatic hydrocarbons, C.sub.10A aromatic hydrocarbons and a bottom heavy tail oil; feeding the bottom heavy tail oil into a post-saturation selective reactor, subjecting to high-selectivity hydrogenation saturation under the conditions of low temperature and low pressure to provide a product having one benzene ring, and then returning the product back to the selective conversion reactor. The full-cut conversion of producing light aromatic hydrocarbon from LCO is achieved, resulting in the technical effects of high yields of monocyclic aromatic hydrocarbons such as benzene-toluene, xylene, C.sub.9A aromatic hydrocarbons, C.sub.10A aromatic hydrocarbons and the like.

A hydrofinishing catalyst according to the present invention includes an amorphous silica-alumina support; and a hydrogenated active metal supported on the support, and has an Al composition having a total mass (wt %) of Al and Si as a denominator and a mass (wt %) of Al as a numerator with respect to a reference line, which is a straight line passing through the center of a cross-section of the support, locations evenly spaced apart along the reference line are sequentially numbered, where composition uniformity, which is defined as UN by the Al composition at the i-th location and an average Al composition at the cross-section of the support passing through the center of the support, is 3.0 or less.

A process for reducing the benzene content of a light reformate refinery stream comprises the following steps: a) reducing the benzene content by exposing the light reformate to hydrogenation conditions in a benzene-saturation reactor bed, b) increasing the octane number of the hydrogenated light reformate produced in step a) by exposing it to isomerization conditions, c) further reducing the benzene content by exposing the light reformate refinery stream to further hydrogenation conditions, wherein the isomerization of step b) occurs after step a), the hydrogenation of step c) does not precede the isomerization step b), and steps a), b) and c) are all carried out within the same reactor.

A process for reducing the benzene content of a light reformate refinery stream comprises the following steps: a) reducing the benzene content by exposing the light reformate to hydrogenation conditions in a benzene-saturation reactor bed, b) increasing the octane number of the hydrogenated light reformate produced in step a) by exposing it to isomerization conditions, c) further reducing the benzene content by exposing the light reformate refinery stream to further hydrogenation conditions, wherein the isomerization of step b) occurs after step a), the hydrogenation of step c) does not precede the isomerization step b), and steps a), b) and c) are all carried out within the same reactor.

An improved hydrotreating catalyst and process for making a base oil product wherein the catalyst comprises a base extrudate that includes a high nanopore volume amorphous silica alumina (ASA) and an alumina. The catalyst and process generally involve the use of a high nanopore volume ASA/alumina based catalyst to produce hydrotreated dewaxed base oil products by contacting the catalyst with a hydrocarbon feedstock. The catalyst base extrudate advantageously comprises an amorphous silica alumina having a pore volume in the 11-20 nm pore diameter range of 0.2 to 0.9 cc/g and an alumina having a pore volume in the 11-20 nm pore diameter range of 0.01 to 1.0 cc/g, with the base extrudate formed from the amorphous silica alumina and the alumina having a total pore volume in the 2-50 nm pore diameter range of 0.12 to 1.80 cc/g. The catalyst further comprises at least one modifier element from Groups 6 to 10 and Group 14 of the Periodic Table. The catalyst and process provide improved aromatics saturation.