The present disclosure relates to a process for preparing long-chain alkanes and alkenes from alcohols, aldehydes, or both. The process proceeds via acceptorless dehydrogenation and decarbonylative coupling using a supported catalyst.

The present disclosure relates to a process for preparing long-chain alkanes and alkenes from alcohols, aldehydes, or both. The process proceeds via acceptorless dehydrogenation and decarbonylative coupling using a supported catalyst.

A method for processing pentanes obtained from a DIB unit is disclosed. The process can include separating a first stream containing pentanes obtained from a DIB unit, in a separation column to obtain a second stream comprising iso-pentane and a third stream comprising n-pentane and neo-pentane; and subjecting the third stream to a butane isomerization unit producing a fourth stream containing iso-pentane, n-pentane, and neo-pentane.

A method for processing pentanes obtained from a DIB unit is disclosed. The process can include separating a first stream containing pentanes obtained from a DIB unit, in a separation column to obtain a second stream comprising iso-pentane and a third stream comprising n-pentane and neo-pentane; and subjecting the third stream to a butane isomerization unit producing a fourth stream containing iso-pentane, n-pentane, and neo-pentane.

Provided is a catalyst which comprises a compound represented by formula (1) and which exhibits activity for at least one type of reaction selected from among hydrosilylation reaction or hydrogenation reaction with respect to an aliphatic unsaturated bond and hydrosilane reduction reaction with respect to a carbon-oxygen unsaturated bond or a carbon-nitrogen unsaturated bond. Formula (1): M.sub.n(L.sub.m) {M represents Fe, Co, or Ni having an oxidation number of 0, L represents an isocyanide ligand represented by formula (2), n denotes an integer of 1-8, and m denotes an integer of 2-12. Formula (2): (CN).sub.x—R.sup.1 (R.sup.1 represents a mono- to trivalent-organic group having 1-30 carbon atoms, optionally being substituted by a halogen atom, and optionally having interposed therein one or more atoms selected from among O, N, S, and Si; and x denotes an integer of 1-3)}.

Catalytic chemical conversion of carbon dioxide gas combined with a hydrocarbon gas, comprising natural gas, methane, ethane, propane, butane or pentane, over a transition metal oxide, produces organic solvent products. The process converts oxidized carbon compounds to valued organic products and can reduce or eliminate the carbon footprint of industrial electric power generation industry. Catalytic processes are taught for chemical conversion of oxides of carbon, principally carbon dioxide (formed by combustion of hydrocarbons), to solvent compounds comprising acetone, butanol, pentane and related organic products. The catalysts are transition metal oxides, selected from the group comprising manganese, iron and cobalt or combinations thereof.

Provided is a separation membrane that is suitable for use in separating one or more hydrocarbons from a hydrocarbon mixture. More specifically, the separation membrane includes a porous support for which acid content is not substantially detected by ammonia temperature programmed desorption in a temperature range of higher than 450° C. and not higher than 600° C. and a porous separation layer containing a zeolite that is disposed on the porous support.

Provided is a separation membrane that is suitable for use in separating one or more hydrocarbons from a hydrocarbon mixture. More specifically, the separation membrane includes a porous support for which acid content is not substantially detected by ammonia temperature programmed desorption in a temperature range of higher than 450° C. and not higher than 600° C. and a porous separation layer containing a zeolite that is disposed on the porous support.

Hydrodeoxygenating a biorenewable feed that is concentrated in free fatty acids with 10-13 carbon atoms at a moderate hydrodeoxygenation ratio that is less than the ratio of hydrodeoxygenation utilized for traditional biorenewable feeds such as vegetable oil or even mineral feedstocks, normal paraffins in the range desired by the detergents industry can be produced. Either hydroisomerization or an iso-normal separation can be performed to provide green fuel streams. Two reactors are proposed, one for hydrodeoxygenation of the biorenewable feed that is concentrated in free fatty acids with 10-13 carbon atoms and the other for a traditional biorenewable feed or even a mineral feed operated at a higher deoxygenation ratio.

Hydrodeoxygenating a biorenewable feed that is concentrated in free fatty acids with 10-13 carbon atoms at a moderate hydrodeoxygenation ratio that is less than the ratio of hydrodeoxygenation utilized for traditional biorenewable feeds such as vegetable oil or even mineral feedstocks, normal paraffins in the range desired by the detergents industry can be produced. Either hydroisomerization or an iso-normal separation can be performed to provide green fuel streams. Two reactors are proposed, one for hydrodeoxygenation of the biorenewable feed that is concentrated in free fatty acids with 10-13 carbon atoms and the other for a traditional biorenewable feed or even a mineral feed operated at a higher deoxygenation ratio.