Abstract: A method and system for producing ketones, suitable for manufacture of base oil or diesel fuel components, from a feedstock of biological origin containing fatty acids and/or fatty acid derivatives, and being at least partly in liquid form, by subjecting the feedstock to a catalytic ketonisation reaction, wherein the ketonisation reaction is carried out in a system having one or more ketonisation reactor(s) (A?, B?) each with at least one ketonisation catalyst bed (G?). The method and system for producing ketones use a gas containing CO2 produced in the ketonisation reactors as a carrier gas.

Abstract: A process is disclosed for converting levulinic acid to gammavalerolactone with increased selectivity. The process is based on the recognition of the reaction intermediate, 4-hydroxyvaleric acid, and improved conversion thereof.

Abstract: A process is disclosed for converting levulinic acid to gammavalerolactone with increased selectivity. The process is based on the recognition of the reaction intermediate, 4-hydroxyvaleric acid, and improved conversion thereof.

Abstract: Method of producing a hydrocarbon composition in which a biomass raw-material is gasified to produce a raw syngas containing carbon monoxide, carbon dioxide and hydrogen, the hydrogen-to-carbon monoxide ratio being about 0.5 to 1.7. A part of the impurities is removed to produce a clean syngas which is fed into a Fischer-Tropsch reactor where a significant part of the carbon monoxide and hydrogen is converted to a hydrocarbon composition containing C4-C90 hydrocarbons. A hydrocarbon composition is recovered which mainly contains hydrocarbons which are solid or semisolid at ambient temperature and pressure and an off-gas of the Fischer-Tropsch reactor, including hydrocarbons which are gaseous at ambient temperature and pressure, is used for producing hydrogen gas. By introducing hydrogen into the clean syngas, the hydrogen to carbon monoxide ratio can be increased and by using off-gas-produced hydrogen, the capacity of the process is significantly improved.

Abstract: A method for adjusting hydrogen to carbon monoxide ratio of syngas contaminated by sulfur impurities involving a water gas shift (WGS) reaction. In light of the presence of the sulfur impurities, the WGS can be implemented as a sour gas shift. WGS can provide good results by using a non-sulfided catalyst. Conditions can be employed which contribute to further enhanced CO-conversion in the reaction. The hydrocarbons or derivatives thereof obtainable from the method can further be refined and used for production of fuels or lubricants for combustion engines.

Abstract: A method of reforming a gasification gas, in order to decompose the impurities comprised in the gas, and a use of a precious metal catalyst in the pre-reforming of gasification gas. The gas can be brought into contact with a metal catalyst in the presence of an oxidizing agent. The reformation can be carried out in several stages, in which case at least in one of the first catalytic zones a noble metal catalyst can be used, and in a secondary reforming stage which follows the first, preliminary reforming zone, the catalyst that can be used is a metal catalyst. Oxygen can be fed separately into each of the catalyst zones. The use of a noble metal catalyst can reduce the risk of deactivation of the metal catalysts and can increase the operating life of the catalyst.

Abstract: A method for naphthalene removal from a gas using a solid adsorbent material including benzene for the removal. The removal can be applied to, for example, a crude syngas main stream and/or a carbon dioxide exhaust side stream. The adsorption to the adsorbent material can be reversible so that the material can be reused and naphthalene and possibly benzene can be recovered after regeneration.

Abstract: A method for adjusting hydrogen to carbon monoxide ratio of syngas contaminated by sulfur impurities involving a water gas shift (WGS) reaction. In light of the presence of the sulfur impurities, the WGS can be implemented as a sour gas shift. WGS can provide good results by using a non-sulfided catalyst. Conditions can be employed which contribute to further enhanced CO-conversion in the reaction. The hydrocarbons or derivatives thereof obtainable from the method can further be refined and used for production of fuels or lubricants for combustion engines.

Abstract: Method of producing a hydrocarbon composition in which a biomass raw-material is gasified to produce a raw syngas containing carbon monoxide, carbon dioxide and hydrogen, the hydrogen-to-carbon monoxide ratio being about 0.5 to 1.7. A part of the impurities is removed to produce a clean syngas which is fed into a Fischer-Tropsch reactor where a significant part of the carbon monoxide and hydrogen is converted to a hydrocarbon composition containing C4-C90 hydrocarbons. A hydrocarbon composition is recovered which mainly contains hydrocarbons which are solid or semisolid at ambient temperature and pressure and an off-gas of the Fischer-Tropsch reactor, including hydrocarbons which are gaseous at ambient temperature and pressure, is used for producing hydrogen gas. By introducing hydrogen into the clean syngas, the hydrogen to carbon monoxide ratio can be increased and by using off-gas-produced hydrogen, the capacity of the process is significantly improved.

Abstract: A method for dimerizing isobutene, wherein, in dimerizing conditions, the isobutene is brought into contact with a porous cation exchange resin comprising a styrene polymer, which is cross-linked with divinyl benzene, and any sulphonic acid groups adhering to the polymer. The harmful deactivation of this catalyst, which is caused by the accumulation of the oligomers and polymers of isobutene and other C4-olefins in the cation exchange resin catalyst, is essentially decreased by selecting the cation exchange resin from a group including cation exchange resins, the acid,capacity of which is 4.7 equivalents/kg at a minimum, and the portion of divinyl benzene units of which is 5% by weight at a minimum and smaller than 20% by weight.

Abstract: A method for dimerizing isobutene, wherein, in dimerizing conditions, the isobutene is brought into contact with a porous cation exchange resin comprising a styrene polymer, which is cross-linked with divinyl benzene, and any sulphonic acid groups adhering to the polymer. The harmful deactivation of this catalyst, which is caused by the accumulation of the oligomers and polymers of isobutene and other C4-olefins in the cation exchange resin catalyst, is essentially decreased by selecting the cation exchange resin from a group including cation exchange resins, the acid,capacity of which is 4.7 equivalents/kg at a minimum, and the portion of divinyl benzene units of which is 5% by weight at a minimum and smaller than 20% by weight.

Abstract: The invention relates to a method for dimerizing isobutene, wherein, in dimerizing conditions, the isobutene is brought into contact with a porous cation exchange resin comprising a styrene polymer, which is cross-linked with divinyl benzene, and any sulphonic acid groups adhering to the polymer. The harmful deactivation of this catalyst, which is caused by the accumulation of the oligomers and polymers of isobutene and other C4-olefins in the cation exchange resin catalyst, is essentially decreased by selecting the cation exchange resin from a group including cation exchange resins, the acid capacity of which is 4.7 equivalents/kg at a minimum, and the portion of divinyl benzene units of which is 5% by weight at a minimum and smaller than 20% by weight.

Abstract: The invention relates to a method for dimerizing isobutene, wherein, in dimerizing conditions, the isobutene is brought into contact with a porous cation exchange resin comprising a styrene polymer, which is cross-linked with divinyl benzene, and any sulphonic acid groups adhering to the polymer. The harmful deactivation of this catalyst, which is caused by the accumulation of the oligomers and polymers of isobutene and other C4-olefins in the cation exchange resin catalyst, is essentially decreased by selecting the cation exchange resin from a group including cation exchange resins, the acid capacity of which is 4.7 equivalents/kg at a minimum, and the portion of divinyl benzene units of which is 5% by weight at a minimum and smaller than 20% by weight.