Abstract:
A process for the continuous catalytic conversion of organic compounds, that, together with unwanted attendant materials, form a starting substance: first the organic compounds of the starting material are purposely extracted by means of condensed fluids. Then the extract, containing the condensed fluids and organic compounds as the reaction mixture is contacted with a catalyst for the catalytic conversion of the organic compounds to form a product mixture, which contains the individual products of the catalytic conversion. The product mixture is separated from the reaction mixture and the fluids employed are, optionally, conducted back for extraction.
Abstract:
The use of modified silicon dioxide as a catalyst support in catalytic reactions under hydrothermal conditions is described. The pore structure of the supports may be stabilized against hydrothermal reaction conditions by impregnating the catalyst supports with elements of Group IVB of the Periodic Tube of Elements.
Abstract:
A process is disclosed for continuously hydrogenating unsaturated fats, fatty acids or fatty acid esters on a shaped catalyst in a solid bed. The reactants flow over the catalyst in the presence of a medium or solvent mixture in supercritical conditions. This leads to considerably improved activity and selectivity of the hydrogenation reaction compared with conventional trickle bed hydrogenation processes.
Abstract:
A formed copper catalyst for the hydrogenation of organic compounds is disclosed, especially for the selective hydrogenation of furfural to furfuryl alcohol. The catalyst contains an intimate mixture of a pyrogenic silica, reduced copper and, optionally, a basic oxide as promotor. The catalyst is distinguished by a high specific catalytic activity, selectivities and yields.
Abstract:
A catalyst is disclosed made from a porous inorganic carrier material impregnated with a metal component selected from palladium, rhodium, mixtures of palladium and rhodium, and mixtures of palladium and a metal of the copper group, in which the carrier has a bimodal pore radius distribution with a first pore radius distribution maximum in the range of up to 400 .ANG., preferably 50 to 350 .ANG., and with a proportion of at least 20%, relative to the overall pore volume, of macropores having a radius of at least 2,000 .ANG., preferably 5,000 to 20,000 .ANG..
Abstract:
A continuously performable process for the removal or reduction of the nite and/or nitrate content of nitrite-polluted and/or nitrate-polluted water with the selective formation of nitrogen by catalytic hydrogenation. Catalysts suitable for carrying out such a process are also described.
Abstract:
The invention relates to a method for the oxidation of a primary or secondary alcohol, preferably to form an aldehyde or ketone, comprising the following steps: a) providing a catalyst composition comprising at least one compound containing a nitroxyl radical, at least one NO source, at least one carbon or mineral acid or an anhydride of a carbon or mineral acid; b) producing a reaction mixture by adding at least one primary or secondary alcohol and a gas comprising oxygen and optionally one or more than one solvent to the catalyst composition from step a) or step e); c) incubating the reaction mixture from step b) at a temperature of between 0 and 100° C. or at the boiling point of the solvent; d) simultaneously with or subsequent to step c): crystallizing the reaction product; and e) recovering the catalyst composition by removing the crystallized reaction product from the reaction mixture obtained in step d).
Abstract:
The present application relates to a process for removing an organic compound having one or more positive charges from an aqueous solution, comprising the steps a) provision of the aqueous solution comprising the organic compound and of a hydrophobic organic solution which comprises a liquid cation exchanger, where the liquid cation exchanger is hydrophobic, and where the liquid cation exchanger has one or more negative charges and an overall negative charge, b) contacting the aqueous solution and the organic solution, and c) separating off the organic solution from the aqueous solution.
Abstract:
A catalyst for the dehydrogenation of C6.sub.6 -C.sub.15 paraffins is disclosed. The catalyst contains, on a support, at least one platinum group component, at least one promoter component from the group tin, germanium and lead, and at least one additional modifier. The additional modifier contains at least one alkaline earth metal. The stability of the catalyst is essentially higher than that achieved by conventional use of an alkali metal.
Abstract:
A process is disclosed for the selective catalytic hydrogenation of carbonyl groups in aromatic aldehydes of the formula: ##STR1## in which X is carboxyl, methyl or a halogen, to give the corresponding alcohols and methyl compounds. The catalytic hydrogenation is performed with the addition of a solvent optionally in the presence of organic acids on a shaped support catalyst containing a platinum group metal on a support made from titanium oxide in the presence of hydrogen at hydrogen partial pressures of 5 to 50 bar and temperatures of 100.degree. to 300.degree. C.