Chemische Werke Huls Aktiengesellschaft

Chemische Werke Huels Aktiengesellschaft

Huels Aktiengesellschaft

Oxeno Olefinchemie Gmbh

Fritz Obenaus

Wilhelm Droste

Bernhard Scholz

Franz Nierlich

Joachim Neumeister

Wolfgang H Muller

Udo Peters

Jochen Praefke

Gerhard Franz

Michael Zolffel

Rainer Malzkorn

Thomas Wildt

Hans-Jurgen Erberich

Wolf Streubel

Bernd Greving

Heinrich Balke

Otto Reitemeyer

Richard Filipiak

Heinz-Otto Reitemeyer

The invention relates to a process for preparing methyl tert-butyl ether (MTBE) in qualities which are suitable for organic syntheses and for use as a specialty solvent from MTBE in fuel quality.

Preparation of highly pure methyl tert-butyl ether

Olefins are oligomerized by passing a hydrocarbon feedstock mixture containing olefins of from 2 to 8 carbon atoms over a molecular sieve having a pore diameter of from greater than 4 angstroms to 15 angstroms, and then oligomerizing said olefins by passing the hydrocarbon feedstock over a nickel-containing catalyst at a temperature of from 0.degree.to 200.degree. C. and at a pressure of from 1 to 70 bar absolute.

Oligomerization of olefins

A process for the selective hydrogenation of hydrocarbons having three and more carbon atoms and several double bonds or with triple bonds in monoene-containing hydrocarbon mixtures is described. These compounds are selectively hydrogenated to monoenes in a practically quantitative fashion. Before beginning the hydrogenation, a small amount of carbon monoxide and once to twice the stoichiometric quantity of hydrogen are homogeneously dissolved in the hydrocarbon mixture. The mixture is hydrogenated as a homogeneous liquid phase on a fixed palladium catalyst under a moderately high pressure and at a moderately high temperature. No isomerization can be found in the monoenes and no side reactions or secondary reactions occur.

Process for the selective hydrogenation of polyunsaturated hydrocarbons

Tertiary-butanol in an aqueous solution containing from 40 to 90 percent by weight of tertiary butanol in homogeneous and liquid phase is dehydrated at a fixed catalytic bed consisting of a strongly acidic ion exchange resin at a temperature from 80.degree. to 150.degree. C. and at a pressure from 5 to 25 bars for the purpose of producing isobutene by dehydrating tertiary butanol. Thereupon the homogeneous, liquid reaction mixture is fractionated in a distillation sector separate from the reaction chamber, the isobutene being separated from the water and from the unreacted tertiary butanol. The unreacted tertiary butanol is returned as an aqueous solution in a circulating flow rate to the reactor under the conditions that the mixture of fresh-fed tertiary butanol and the circulating tertiary-butanol/water mix contains from 40 to 90 percent by weight of tertiary butanol at the reactor inlet.

Process for producing high purity isobutene by dehydrating tertiary

A process for the simultaneous manufacture of pure methyl tertiary butyl ether (MTBE) and a substantially isotubene-free mixture of C.sub.4 -hydrocarbons, by reacting the isobutene contained in the mixture of C.sub.4 -hydrocarbons with excess methanol in the liquid phase at elevated temperatures on strongly acid, macroporous, organic ion exchange resins. The process has the following steps:

Process for the simultaneous manufacture of pure MTBE and a

Process for the preparation of pure methyl tert.-butyl ether. Isobutene or isobutene-containing hydrocarbon mixtures are reacted with methanol in a molar ratio of 1:1 to 1:2 in the liquid phase at temperatures of between 30.degree. and 100.degree. C. on sulfonated, strongly acidic, macroporous organic ion exchange resins. After separation of the unreacted hydrocarbons, the reaction mixture is distilled under pressure; the methanol-containing distillate formed during the distillation is recycled into the zone of the reaction between methanol and isobutene; and pure methyl tert.-butyl ether is withdrawn from the sump of the distillation column.

Process for preparing pure methyl tert.-butyl ether

In an improved process for the production of carboxylic acid esters by catalytic oxidation of alcohols in the liquid phase, primary alcohols of 1-4 carbon atoms are oxidized with molecular oxygen at temperatures of about 100.degree.-250.degree. C. in the presence of catalytic amounts of a compound of Co, Mn, Cr, or Fe, and an acid having a first dissociation constant K.sub.1 greater than 10.sup.-3, dissolved in the reaction mixture.

Process for the production of carboxylic acid esters by catalytic

Acetone is produced by the catalytic, oxidative decarbonylation of isobutyraldehyde in the gaseous phase by contacting a gaseous mixture of 1-15% by volume of isobutyraldehyde, at least a stoichiometric amount and up to about 30% by volume of oxygen, and an inert diluent, with a copper oxide catalyst.

Growing community of inventors

Marl, Germany

Fritz Obenaus