A process for the preparation of a catalyst from a catalytic precursor comprising a support based on alumina and/or silica-alumina and/or zeolite and comprising at least one element of group VIB and optionally at least one element of group VIII, by impregnation of said precursor with a solution of a C1-C4 dialkyl succinate. An impregnation step for impregnation of said precursor which is dried, calcined or regenerated, with at least one solution containing at least one carboxylic acid other than acetic acid, then maturing and drying at a temperature less than or equal to 200° C., optionally a heat treatment at a temperature lower than 350° C., followed by an impregnation step with a solution containing at least one C1-C4 dialkyl succinate followed by maturing and drying at a temperature less than 200° C. without subsequent calcination step. The catalyst is used in hydrotreatment and/or hydroconversion.

A process for the preparation of a catalyst from a catalytic precursor comprising a support based on alumina and/or silica-alumina and/or zeolite and comprising at least one element of group VIB and optionally at least one element of group VIII, by impregnation of said precursor with a solution of a C1-C4 dialkyl succinate. An impregnation step for impregnation of said precursor which is dried, calcined or regenerated, with at least one solution containing at least one carboxylic acid other than acetic acid, then maturing and drying at a temperature less than or equal to 200° C., optionally a heat treatment at a temperature lower than 350° C., followed by an impregnation step with a solution containing at least one C1-C4 dialkyl succinate followed by maturing and drying at a temperature less than 200° C. without subsequent calcination step. The catalyst is used in hydrotreatment and/or hydroconversion.

Redox catalysts having surface medication, methods of making redox catalysts with surface modification, and uses of the surface modified redox catalysts are provided. In some aspects, the redox catalysts include a core oxygen carrier region such as CaMnO.sub.3, BaMnO.sub.3−δ, SrMnO.sub.3−δ, Mn.sub.2SiO.sub.4, Mn.sub.2MgO.sub.4−δ, La.sub.0.8Sr.sub.0.2O.sub.3−δ, La.sub.0.8Sr.sub.0.2FeO.sub.3−δ, Ca.sub.9Ti.sub.0.1Mn.sub.0.9O.sub.3−δ, Pr.sub.6O.sub.11−δ, manganese ore, or a combination thereof; and an outer shell having an average thickness of about 1-100 monolayers surrounding the outer surface of the core region. The outer shell can include, for example a salt selected such as Li.sub.2WO.sub.4, Na.sub.2WO.sub.4, K.sub.2WO.sub.4, SrWO.sub.4, Li.sub.2MoO.sub.4, Na.sub.2MoO.sub.4, K.sub.2MoO.sub.4, CsMoO.sub.4, Li.sub.2CO.sub.3, Na.sub.2CO.sub.3, K.sub.2CO.sub.3, or a combination thereof.

A composition of fuel gas that when mixed with spent catalyst and oxygen has an induction time that allows bubbles to break up while combusting in the regenerator. Bubble breakage in a dense bed avoids generation of a flame that can generate hot spots in the regenerator which can damage equipment and catalyst. The fuel gas can be obtained from paraffin dehydrogenation products, so it can sustain operation of the unit even in remote locations. Heavier streams can be mixed with lighter streams to obtain a fuel gas composition with a desirable induction time to avoid such hot spots. Mixing of a depropanizer bottom stream and/or deethanizer overhead stream with lighter gas streams such as cold box light gas or PSA tail gas can provide the desired fuel gas composition.

A composition of fuel gas that when mixed with spent catalyst and oxygen has an induction time that allows bubbles to break up while combusting in the regenerator. Bubble breakage in a dense bed avoids generation of a flame that can generate hot spots in the regenerator which can damage equipment and catalyst. The fuel gas can be obtained from paraffin dehydrogenation products, so it can sustain operation of the unit even in remote locations. Heavier streams can be mixed with lighter streams to obtain a fuel gas composition with a desirable induction time to avoid such hot spots. Mixing of a depropanizer bottom stream and/or deethanizer overhead stream with lighter gas streams such as cold box light gas or PSA tail gas can provide the desired fuel gas composition.

An oxygen gas stream is distributed to a spent catalyst stream through an oxygen nozzle of an oxygen gas distributor and a fuel gas stream is distributed to the spent catalyst stream through a fuel nozzle of a fuel gas distributor. An oxygen gas jet generated from said oxygen nozzle and a fuel gas jet generated from said fuel gas nozzle have the same elevation in the regenerator. In a regenerator, an oxygen gas distributor and a fuel gas distributor may be located in a mixing chamber. A fuel outlet of a fuel nozzle of the fuel gas distributor may be within a fifth of the height of the mixing chamber from an oxygen outlet of an oxygen nozzle of the oxygen gas distributor. In addition, clear space is provided between a fuel gas nozzle on a fuel gas distributor and a closest oxygen nozzle on an oxygen gas distributor.

An oxygen gas stream is distributed to a spent catalyst stream through an oxygen nozzle of an oxygen gas distributor and a fuel gas stream is distributed to the spent catalyst stream through a fuel nozzle of a fuel gas distributor. An oxygen gas jet generated from said oxygen nozzle and a fuel gas jet generated from said fuel gas nozzle have the same elevation in the regenerator. In a regenerator, an oxygen gas distributor and a fuel gas distributor may be located in a mixing chamber. A fuel outlet of a fuel nozzle of the fuel gas distributor may be within a fifth of the height of the mixing chamber from an oxygen outlet of an oxygen nozzle of the oxygen gas distributor. In addition, clear space is provided between a fuel gas nozzle on a fuel gas distributor and a closest oxygen nozzle on an oxygen gas distributor.

This disclosure relates to systems and processes for reducing CO.sub.2 emissions produced by the regenerator reactor of the fluid catalytic cracking process.

The present invention relates to a hydrocarbon conversion process comprising contacting a hydrocarbon feed stream with a hydrocarbon conversion catalyst, wherein the hydrocarbon conversion catalyst comprises a first composition comprising a dehydrogenation active metal on a solid support; and a second composition comprising a transition metal and a doping agent on an inorganic support, wherein the doping agent is selected from zinc, gallium, indium, lanthanum, and mixtures thereof.

A composite comprises a carbonaceous and a metallic nanotube conjugated with a carbonaceous support. The composite may be used to remove contaminants from water.