Catalytic hydrogenation process

Details Catalytic hydrogenation process Catalytic hydrogenation process

1990-06-04

1992-03-03

Evans, J. E.

Organic compounds -- part of the class 532-570 series

Organic compounds

Oxygen containing

260409, 260413, 564420, 508835, 508861, 508863, 585266, C07C 29141, C07C 29145, C07C 29149, C07C 510

Patent

active

050935356

DESCRIPTION:

BRIEF SUMMARY
This invention relates to a liquid phase catalytic hydrogenation process.
Heterogeneous catalytic hydrogenation processes of various kinds are widely practised on a commercial scale and are used for hydrogenation of a wide variety of organic feedstocks. Typically such hydrogenation reactions are conducted at a pressure of from about 1 bar to about 300 bar and at a temperature in the range of from about 40.degree. C. to about 380.degree. C. Examples include hydrogenation of aldehydes to alcohols, of unsaturated hydrocarbons to saturated hydrocarbons, of acetylene-derived chemicals to saturated materials, of unsaturated fatty acids to saturated fatty acids, of ketones to secondary alcohols, of esters of unsaturated fatty acids to esters of partially or fully hydrogenated fatty acids, of nitriles to primary amines, and of certain sugars to polyhydroxyalcohols. Also worthy of mention is the hydrogenation of quinones, for example the hydrogenation of 2-ethylanthraquinone as a step in the production of hydrogen peroxide. This cyclohexanol is produced commercially by catalytic hydrogenation of cyclohexanone, and iso-propanol by catalytic hydrogenation of acetone. An example of hydrogenation of an unsaturated hydrocarbon is the production of cyclohexane from benzene. Typical catalysts for such hydrogenation reactions include Group VIII metal catalysts, such as nickel, palladium and platinum. Production of butane-1,4-diol by hydrogenation of but-2-yn-1,4-diol is an example of hydrogenation of an acetylene-derived chemical. A suitable catalyst for this reaction has been described as a granular nickel-copper-manganese on silica gel. The production of stearic acid by catalytic hydrogenation of the corresponding unsaturated acids, linoleic acid and linolenic acid, at a temperature of about 150.degree. C. and at a pressure of about 14.75 bar to about 32 bar and using a nickel, cobalt, platinum, palladium, chromium or copper/zinc catalyst, is an example of the hydrogenation of unsaturated fatty acids to yield saturated fatty acids. So-called "hardening" of vegetable oils is an example of hydrogenation of esters of unsaturated fatty acids. Production of beta-phenylethylamine by hydrogenation of benzyl cyanide is an example of hydrogenation of a nitrile. As examples of hydrogenation of sugars to polyhydroxyalcohols there can be mentioned hydrogenation of ketose and aldose sugars to hexahydroxyalcohols, for example hydrogenation of D-glucose to sorbitol and of D-mannose to mannitol.
An important route to C.sub.3 and higher alkanols involves hydroformylation of alpha-olefins, such as ethylene, propylene, and butene-1, to yield the corresponding aldehyde having one more carbon atom than the starting olefin. Thus ethylene yields propionaldehyde and propylene yields a mixture of n- and iso-butyraldehyde (with the n-isomer usually predominating). These aldehydes yield the corresponding alkanols, e.g. n-propanol and n-butanol, upon catalytic hydrogenation. The important plasticiser alcohol, 2-ethylhexanol, is made by alkali-catalysed condensation of n-butyraldehyde to yield the unsaturated aldehyde, 2-ethyl-hex-2-enal, which is then hydrogenated to yield the desired 2-ethylhexanol. Although the preferred catalysts for such aldehyde hydrogenation reactions used to be Group VIII metal catalysts, such as nickel, palladium or platinum, the use of a solid catalyst comprising a reduced mixture of CuO and ZnO under vapour phase conditions has also been proposed (see EP-A-0008767 and U.S. Pat. No. 2,549,416). Molybdenum sulphide supported on an activated carbon carrier has also been suggested in GB-A-765972. The hydrogenation of an aldehyde feed containing ring-type sulphur compounds using a reduced mixture of oxides or hydroxides of copper and zinc is described in U.S. Pat. No. 4,052,467. Copper chromite has also been used as an aldehyde hydrogenation catalyst.
Hydrodesulphurisation is another commercially important hydrogenation reaction. This is the removal complex organic sulphur compounds, such as sulphides, disulphides, benzothioph

REFERENCES:
patent: 3880940 (1975-09-01), Baer et al.
patent: 4288640 (1981-09-01), Schuster et al.
patent: 4451677 (1984-05-01), Bradley et al.
patent: 4510092 (1985-04-01), Rosen
patent: 4626604 (1986-12-01), Hiles et al.
patent: 4960960 (1990-10-01), Harrison et al.

Affiliated with

Also associated with

Rating

Catalytic hydrogenation process does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Catalytic hydrogenation process, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Catalytic hydrogenation process will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-273745