An oxygen transfer agent comprising a metal-boron oxide is provided. The average oxidation state of the metal in the metal-boron oxide is about 3+, and has 10% or less of a stoichiometric excess in moles of Mn with respect to the boron. The oxygen transfer agent may further comprise a magnesia-phosphate cement. The oxygen transfer agent is capable of oxidatively dehydrogenating a hydrocarbon feed at reaction conditions to produce a dehydrogenated hydrocarbon product and water. The oxidative dehydrogenation can take place under reaction conditions of less than 1000 ppm weight molecular oxygen, or in the presence of more than 1000 ppm weight of molecular oxygen. Also provided are methods of using the oxygen transfer agents, and an apparatus for effecting the oxidative dehydrogenation of the hydrocarbon feed.

[Problem to be Solved] To provide a catalyst having hydrotreatment (hydrogenation, desulfurization and denitrogenation) performance that is equal to or superior to the prior art, as a hydrotreating catalyst for hydrocarbon oils, and a hydrotreating process for hydrocarbon oils using the catalyst. [Means to Solve the Problem] A hydrotreating catalyst for hydrocarbon oils comprising, at least one metal selected from the group 6 of the periodic table, at least one metal selected from the groups 8 to 10 of the periodic table, and optionally further phosphorus and/or boron as catalytic active components supported on an inorganic porous support based on alumina, wherein the inorganic porous support comprises, as constituent components thereof, silica in an amount of less than 1% by mass with respect to the mass of the oxide and a metal of the group 4 of the periodic table in an amount of less than 13% by mass as an oxide; wherein the metal of the group 4 of the periodic table is highly dispersed in the inorganic porous support, a degree of dispersion thereof is shown by that no peak is substantially observed in the wave number range of 100 to 200 cm.sup.−1 by Raman spectroscopy and that no crystal is substantially observed by X-ray diffraction analysis; wherein the hydrotreating catalyst has a specific surface area of 100 to 300 m.sup.2/g, a pore volume of 0.2 to 0.5 ml/g, an average pore diameter of 6 to 10 nm, and a NO adsorption amount of 4.5 cm.sup.3/ml or more as catalytic characteristics; and wherein no crystals derived from the metal oxide salts of the group 6 of the periodic table are not substantially observed by X-ray diffraction analysis.

[Problem to be Solved] To provide a catalyst having hydrotreatment (hydrogenation, desulfurization and denitrogenation) performance that is equal to or superior to the prior art, as a hydrotreating catalyst for hydrocarbon oils, and a hydrotreating process for hydrocarbon oils using the catalyst. [Means to Solve the Problem] A hydrotreating catalyst for hydrocarbon oils comprising, at least one metal selected from the group 6 of the periodic table, at least one metal selected from the groups 8 to 10 of the periodic table, and optionally further phosphorus and/or boron as catalytic active components supported on an inorganic porous support based on alumina, wherein the inorganic porous support comprises, as constituent components thereof, silica in an amount of less than 1% by mass with respect to the mass of the oxide and a metal of the group 4 of the periodic table in an amount of less than 13% by mass as an oxide; wherein the metal of the group 4 of the periodic table is highly dispersed in the inorganic porous support, a degree of dispersion thereof is shown by that no peak is substantially observed in the wave number range of 100 to 200 cm.sup.−1 by Raman spectroscopy and that no crystal is substantially observed by X-ray diffraction analysis; wherein the hydrotreating catalyst has a specific surface area of 100 to 300 m.sup.2/g, a pore volume of 0.2 to 0.5 ml/g, an average pore diameter of 6 to 10 nm, and a NO adsorption amount of 4.5 cm.sup.3/ml or more as catalytic characteristics; and wherein no crystals derived from the metal oxide salts of the group 6 of the periodic table are not substantially observed by X-ray diffraction analysis.

Methods for making a supported chromium catalyst are disclosed, and can comprise contacting a silica-coated alumina containing at least 30 wt. % silica with a chromium-containing compound in a liquid, drying, and calcining in an oxidizing atmosphere at a peak temperature of at least 650° C. to form the supported chromium catalyst. The supported chromium catalyst can contain from 0.01 to 20 wt. % chromium, and typically can have a pore volume from 0.5 to 2 mL/g and a BET surface area from 275 to 550 m.sup.2/g. The supported chromium catalyst subsequently can be used to polymerize olefins to produce, for example, ethylene-based homopolymers and copolymers having high molecular weights and broad molecular weight distributions.

Methods for making a supported chromium catalyst are disclosed, and can comprise contacting a silica-coated alumina containing at least 30 wt. % silica with a chromium-containing compound in a liquid, drying, and calcining in an oxidizing atmosphere at a peak temperature of at least 650° C. to form the supported chromium catalyst. The supported chromium catalyst can contain from 0.01 to 20 wt. % chromium, and typically can have a pore volume from 0.5 to 2 mL/g and a BET surface area from 275 to 550 m.sup.2/g. The supported chromium catalyst subsequently can be used to polymerize olefins to produce, for example, ethylene-based homopolymers and copolymers having high molecular weights and broad molecular weight distributions.

A modular device for generating hydrogen gas from a hydrogen liquid carrier may include a housing; an inlet for receiving the hydrogen liquid carrier; and at least one cartridge arranged within the housing. The cartridge may include at least one catalyst configured to cause a release of hydrogen gas when exposed to the hydrogen liquid carrier. The modular device may include a gas outlet for expelling the hydrogen gas released in the modular device and a liquid outlet for expelling spent hydrogen liquid carrier.

The invention relates to a catalyst comprising a support, at least one noble metal M, tin, phosphorus and yttrium, the content of phosphorus element being less than or equal to 1% by weight, and the content of yttrium being less than or equal to 1% by weight relative to the mass of the catalyst. The invention also relates to the process for preparing the catalyst and to the use thereof in reforming.

The invention relates to a catalyst comprising a support, at least one noble metal M, tin, phosphorus and yttrium, the content of phosphorus element being less than or equal to 1% by weight, and the content of yttrium being less than or equal to 1% by weight relative to the mass of the catalyst. The invention also relates to the process for preparing the catalyst and to the use thereof in reforming.

A system for continuously treating recycled polymeric material includes a hopper configured to feed the recycled polymeric material into the system. An extruder can turn the recycled polymeric material in a molten material. In some embodiments, the extruder uses thermal fluids, electric heaters, and/or a separate heater. The molten material is depolymerized in a reactor. In some embodiments, a catalyst is used to aid in depolymerizing the material. In certain embodiments, the catalyst is contained in a permeable container. The depolymerized molten material can then be cooled via a heat exchanger. In some embodiments, multiple reactors are used. In certain embodiments, these reactors are connected in series. In some embodiments, the reactor(s) contain removable static mixer(s) and/or removable annular inserts.

A system for continuously treating recycled polymeric material includes a hopper configured to feed the recycled polymeric material into the system. An extruder can turn the recycled polymeric material in a molten material. In some embodiments, the extruder uses thermal fluids, electric heaters, and/or a separate heater. The molten material is depolymerized in a reactor. In some embodiments, a catalyst is used to aid in depolymerizing the material. In certain embodiments, the catalyst is contained in a permeable container. The depolymerized molten material can then be cooled via a heat exchanger. In some embodiments, multiple reactors are used. In certain embodiments, these reactors are connected in series. In some embodiments, the reactor(s) contain removable static mixer(s) and/or removable annular inserts.