A method for separation of at least one catalyst or adsorbent from a homogeneous mixture of catalysts or adsorbents, used in a method for treatment of gas or hydrocarbon feedstock, in which the grains of catalysts or adsorbents are separated according to a sorting threshold corresponding to a content of the constituent element that is sought and defined by the user.

The disclosed invention relates to a method for restarting a synthesis gas conversion process which has stopped. The synthesis gas conversion process may be conducted in a conventional reactor or a microchannel reactor. The synthesis gas conversion process may comprise a process for converting synthesis gas to methane, methanol or dimethyl ether. The synthesis gas conversion process may be a Fischer-Tropsch process.

The disclosed invention relates to a method for restarting a synthesis gas conversion process which has stopped. The synthesis gas conversion process may be conducted in a conventional reactor or a microchannel reactor. The synthesis gas conversion process may comprise a process for converting synthesis gas to methane, methanol or dimethyl ether. The synthesis gas conversion process may be a Fischer-Tropsch process.

The invention provides a catalyst system and method for the deoxygenation of hydrocarbons, such as bio-oil, using a sulphide-sulfate or an oxide-carbonate (LDH) system. The invention extends to a pyrolysis process of a carbonaceous bio-mass wherein a first combustion zone is carried out in one or more combustion fluidised beds in which a particulate material including chemically looping deoxygenation catalyst particles is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles, including the catalyst particles, heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at a temperature of from 250 C. to 1100 C., typically around 900 C., and the pyrolysis zone being operated at a temperature of from 250 C. to 900 C., typically 450 C. to 600 C., said catalyst particles being oxygenated in the pyrolysis zone in the presence of oxygenates in the pyrolysis oil and regenerated in the combustion zone either by calcining to drive off the carbon oxides, such as CO.sub.2, or by reduction to its form which is active for deoxygenation of the pyrolysis oil.

The invention provides a catalyst system and method for the deoxygenation of hydrocarbons, such as bio-oil, using a sulphide-sulfate or an oxide-carbonate (LDH) system. The invention extends to a pyrolysis process of a carbonaceous bio-mass wherein a first combustion zone is carried out in one or more combustion fluidised beds in which a particulate material including chemically looping deoxygenation catalyst particles is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles, including the catalyst particles, heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at a temperature of from 250 C. to 1100 C., typically around 900 C., and the pyrolysis zone being operated at a temperature of from 250 C. to 900 C., typically 450 C. to 600 C., said catalyst particles being oxygenated in the pyrolysis zone in the presence of oxygenates in the pyrolysis oil and regenerated in the combustion zone either by calcining to drive off the carbon oxides, such as CO.sub.2, or by reduction to its form which is active for deoxygenation of the pyrolysis oil.

The disclosed invention relates to a method for restarting a synthesis gas conversion process which has stopped. The synthesis gas conversion process may be conducted in a conventional reactor or a microchannel reactor. The synthesis gas conversion process may comprise a process for converting synthesis gas to methane, methanol or dimethyl ether. The synthesis gas conversion process may be a Fischer-Tropsch process.

The disclosed invention relates to a method for restarting a synthesis gas conversion process which has stopped. The synthesis gas conversion process may be conducted in a conventional reactor or a microchannel reactor. The synthesis gas conversion process may comprise a process for converting synthesis gas to methane, methanol or dimethyl ether. The synthesis gas conversion process may be a Fischer-Tropsch process.

The present disclosure describes a non-destructive process for removing metals, metal ions and metal oxides present in alumina-based materials without destroying alumina, allowing the regeneration of alumina-based catalysts. Known conventional procedures and/or methods for removing metals, metal ions and metal oxides present in alumina-based materials use some inorganic acid or its mixtures to carry out digestion, which modifies the properties of alumina and those of any other element contained in the material, destroying alumina and preventing its reuse. The present disclosure is characterized by using an extracting agent that sequesters metals, metal ions and/or metal oxides present in alumina-based materials without modifying their properties. The employed extracting agent is an alcohol. The non-destructive process introduced in the present invention reaches metal (M) removal rates of at least 42% when using a continuous flow reactor and of at least 27% when a batch reactor is employed.

The present disclosure describes a non-destructive process for removing metals, metal ions and metal oxides present in alumina-based materials without destroying alumina, allowing the regeneration of alumina-based catalysts. Known conventional procedures and/or methods for removing metals, metal ions and metal oxides present in alumina-based materials use some inorganic acid or its mixtures to carry out digestion, which modifies the properties of alumina and those of any other element contained in the material, destroying alumina and preventing its reuse. The present disclosure is characterized by using an extracting agent that sequesters metals, metal ions and/or metal oxides present in alumina-based materials without modifying their properties. The employed extracting agent is an alcohol. The non-destructive process introduced in the present invention reaches metal (M) removal rates of at least 42% when using a continuous flow reactor and of at least 27% when a batch reactor is employed.

A used denitration catalyst is regenerated by means of a method comprising bringing the used denitration catalyst comprising titanium oxide as an essential ingredient into contact with a suspension of particles comprising manganese oxide, subjecting the resulting product to a liquid draining, and subjecting the liquid-drained product to a drying process, additionally, further comprising impregnating a solution comprising a compound containing at least one element selected from the group consisting of vanadium, molybdenum and tungsten into the denitration catalyst after the drying process, and subjecting the impregnated product to a drying treatment.