A catalyst composition includes a metal catalyst dispersed in a molten eutectic mixture of alkali metal or alkaline earth metal carbonates or hydroxides. A process for the catalytic cracking of hydrocarbons includes contacting in a reactor system a carbon-containing feedstock with at least one catalyst in the presence of oxygen to generate olefinic and/or aromatic compounds; and collecting the olefinic and/or aromatic compounds; wherein: the at least one catalyst includes a metal catalyst dispersed in a molten eutectic mixture of alkali metal or alkaline earth metal carbonates or hydroxides. A process for preparing the catalyst includes mixing metal catalyst precursors selected from transition metal compounds and rare-earth metal compounds and a eutectic mixture of alkali metal or alkaline earth metal carbonates or hydroxides and heating it. A use of the catalyst in the catalytic cracking process of hydrocarbons.

A catalyst composition includes a metal catalyst dispersed in a molten eutectic mixture of alkali metal or alkaline earth metal carbonates or hydroxides. A process for the catalytic cracking of hydrocarbons includes contacting in a reactor system a carbon-containing feedstock with at least one catalyst in the presence of oxygen to generate olefinic and/or aromatic compounds; and collecting the olefinic and/or aromatic compounds; wherein: the at least one catalyst includes a metal catalyst dispersed in a molten eutectic mixture of alkali metal or alkaline earth metal carbonates or hydroxides. A process for preparing the catalyst includes mixing metal catalyst precursors selected from transition metal compounds and rare-earth metal compounds and a eutectic mixture of alkali metal or alkaline earth metal carbonates or hydroxides and heating it. A use of the catalyst in the catalytic cracking process of hydrocarbons.

[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.

Systems and methods of synthesizing nanoparticles on substrates using rapid, high temperature thermal shock. A method involves depositing micro-sized particles or salt precursors on a substrate, and applying a rapid, high temperature thermal shock to the micro-sized particles or the salt precursors to become nanoparticles on the substrate. A system may include a rotatable member that receives a roll of a substrate sheet having micro-sized particles or salt precursors; a motor that rotates the rotatable member so as to unroll the substrate; and a thermal energy source that applies a short, high temperature thermal shock to the substrate. The nanoparticles may be metallic, ceramic, inorganic, semiconductor, or compound nanoparticles. The substrate may be a carbon-based substrate, a conducting substrate, or a non-conducting substrate. The high temperature thermal shock process may be enabled by electrical Joule heating, microwave heating, thermal radiative heating, plasma heating, or laser heating.

Systems and methods of synthesizing nanoparticles on substrates using rapid, high temperature thermal shock. A method involves depositing micro-sized particles or salt precursors on a substrate, and applying a rapid, high temperature thermal shock to the micro-sized particles or the salt precursors to become nanoparticles on the substrate. A system may include a rotatable member that receives a roll of a substrate sheet having micro-sized particles or salt precursors; a motor that rotates the rotatable member so as to unroll the substrate; and a thermal energy source that applies a short, high temperature thermal shock to the substrate. The nanoparticles may be metallic, ceramic, inorganic, semiconductor, or compound nanoparticles. The substrate may be a carbon-based substrate, a conducting substrate, or a non-conducting substrate. The high temperature thermal shock process may be enabled by electrical Joule heating, microwave heating, thermal radiative heating, plasma heating, or laser heating.

The present invention is a method for removing sulfur from liquid hydrocarbon feedstocks and for performing hydrogenation reactions in sulfur-contaminated feedstocks, including the hydrogenation of naphthalene in the presence of sulfur compounds, using catalysts or adsorbents comprising metal oxide nanowires decorated with reduced catalytically-active metal particles. In a preferred embodiment, the adsorbent comprises zinc oxide nanowires decorated with catalytically-active metals selected from nickel, cobalt, molybdenum, platinum, palladium, copper, oxides thereof, alloys thereof, and combinations thereof. In some embodiments, the sulfur is removed through a desulfurization process without an external hydrogen supply. The process is effective for the removal of sulfur from diesel fuels and liquid fuel streams, and for deep desulfurization of natural gas streams. The process is also effective for the selective hydrogenation of naphthalene to tetralin in the presence of sulfur compounds.

The present invention is a method for removing sulfur from liquid hydrocarbon feedstocks and for performing hydrogenation reactions in sulfur-contaminated feedstocks, including the hydrogenation of naphthalene in the presence of sulfur compounds, using catalysts or adsorbents comprising metal oxide nanowires decorated with reduced catalytically-active metal particles. In a preferred embodiment, the adsorbent comprises zinc oxide nanowires decorated with catalytically-active metals selected from nickel, cobalt, molybdenum, platinum, palladium, copper, oxides thereof, alloys thereof, and combinations thereof. In some embodiments, the sulfur is removed through a desulfurization process without an external hydrogen supply. The process is effective for the removal of sulfur from diesel fuels and liquid fuel streams, and for deep desulfurization of natural gas streams. The process is also effective for the selective hydrogenation of naphthalene to tetralin in the presence of sulfur compounds.

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 present invention relates to a process for preparing alkanolamines and ethyleneamines in the liquid phase, by reacting ethylene glycol and/or monoethanolamine with ammonia in the presence of an amination catalyst which is obtained by reducing a catalyst precursor, wherein the preparation of the catalyst precursor comprises a step a) in which a catalyst precursor comprising one or more catalytically active components of Sn, Cu and Ni, and a step b) in which the catalyst precursor prepared in step a) is contacted with a soluble Re compound.