Wacker-chemie Gmbh

Degussa - Huls Ag

Klaus Haselwarter

Ludwig Schmidhammer

Gerhard Dummer

Rudolf Strasser

Hermann Klaus

Klaus-Peter Mohr

Eduard Pichl

Albin Frank

Stefan Bosing

A supported catalyst includes: a) 0.5-15 wt. % of one or more Cu-II compounds, the quantitative amounts referring to copper metal; b) 0.1-8 wt. % of one or more alkali metal compounds, the quantitative amounts referring to alkali metal; c) 0.1-10 wt. % of an oxide mixture including; c1) 80-95 mole % of oxides of cerite rare earths with atomic Nos. 57 to 62, except promethium, and c2) 5-20 mole % of zirconium dioxide, where c1) and c2) must together total 100 mole % and the quantitative amount of c) refers to the oxides of the mixture, and d) the remainder up to 100 wt. % being .gamma. and/or .alpha.-aluminum oxide as support material, wherein e) the support material d) has a total pore volume in the range from 0.65 to 1.2 cm.sup.3 /g, and wherein f) the supported catalyst is present in the form of cylindrical hollow bodies having at least one passage channel, the ratio of height h to external diameter d.sup.e being less than 1.5 for diameters d.sub.e of up to 6 mm, and the ratio h/d.sub.e being less than 0.6 for diameter d.sub.e greater than 6 mm. A process for producing the supported catalyst is also described.

Supported catalyst, process for its production as well as its use in the

A catalyst system for the preparation of 1,2-dichloroethane by reacting ethylene and chlorine in a solvent, if desired, in the presence of an inhibitor for reducing the formation of byproducts. The catalyst system comprises a phenolate/chlorine complex. The invention also relates to a process for the chlorination of ethylene using indicated catalyst system.

Catalyst system and use for the preparation of 1,2-dichloroethane

The invention relates to a process for purifying unreacted 1,2-dichloroethane from a 1,2-dichloroethane pyrolysis process by chlorinating the benzene produced as a by-product and removing the chlorination products by distillation.

Process for purifying unreacted 1,2-dichloroethane from a

In a method of treating the reaction product of pyrolysis of 1,2-dichloroethane to form vinyl chloride and hydrogen chloride with multiple stage cooling and distillation separation of the reaction product and recycle of unreacted 1,2-dichloroethane to the pyrolysis step, the improvement comprising direct cooling of the reaction product immediately after leaving the pyrolysis step, within 1 sec from a temperature range of 480.degree. to 540.degree. C. down to 150.degree. to 250.degree. C., charging the cooled product into a quench column, recovering the vapors from the head of the quench column and indirectly cooling the same by heat exchange to at least its condensation point, the heat exchange media being at least one member of the group consisting of (a) 1,2-dichloroethane to be fed in heated condition to the pyrolysis unit, (b) air used as combustion air to fire the pyrolysis zone, (c) the sump of the hydrogen chloride column as defined above, (d) liquid hydrogene chloride to be evaporated and, (e) water, to dissipate heat not used within the measures according to the present invention.

Heat recovery in production of vinyl chloride by pyrolysis of

An improved method of producing vinyl chloride by pyrolysis of purified 1,2-dichloroethane at temperatures from 480.degree. C. to 540.degree. C. at a pressure of 10 to 36 bar absolute with partial utilization of the heat content of the flue gases from the pyrolysis furnace firing to preheat liquid 1,2-dichloroethane almost to its boiling temperature utilizing the flue gas waste heat to generate steam, cool the pyrolysis gas mixture in several stages and separate the hydrogen chloride from the pyrolysis gas mix in a hydrogen chloride column as well as separate vinyl chloride from the pyrolysis gas mix in a vinyl chloride monomer column.

Vinyl chloride production

An improved process for the preparation of vinyl chloride from 1,2-dichloroethane (EDC) wherein 0.10 to 0.15 % by weight of carbon tetrachloride based on EDC, is used as a cracking promoter and the CHCl.sub.3 content is limited to less than 200 ppm. Before being fed to the cracking zone, the EDC is brought almost to the boiling point at 15 to 31 bar and then expanded to 10 to 16 bar with flashing EDC vapors and the fraction which has remained liquid is vaporized externally, and the combined EDC gas streams are heated, after being fed into the cracking furnaces, so that the energy required for cracking is already supplied in the first 75 to 85% of the reaction zone, whereby a conversion of 60 to 70% is obtained at residence time from 10 to 25 seconds and the exit temperature from the reaction zone is 485.degree. to 510.degree. C.

Process for thermal cracking of 1,2-dichloroethane to form vinyl chloride

A process of upgrading hydrogen chloride which contains chlorine, iron-III-chloride, acetylene and/or ethylene, for use in an oxichlorination process, wherein water in a gaseous state is added to the hydrogen chloride at temperatures between 120.degree. and 180.degree. C. within a time period of maximally 0.9 seconds after the acetylene and/or ethylene is present in the hydrogen chloride, together with chlorine and iron-III-chloride.

Process for upgrading hydrogen chloride containing chlorine,

A process for the work-up of chlorination residues by dissolving the same at temperatures between 100.degree. and 180.degree. C. in chlorine- and oxygen-containing hydrocarbons having a ratio by weight of hydrogen to chlorine of 0.028-0.06:1, a ratio by weight of oxygen:carbon of 0.0038-0.0089:1, and an atomic ratio of carbon:hydrogen of 1:1.1-1.9 and/or in hydrocarbons, boiling between 160.degree. and 380.degree. C. at one bar abs. and having an atomic ratio carbon:hydrogen of 1:1.85-2.0 so as to obtain a liquid preparation having a ratio by weight of hydrogen:chlorine of 0.028-0.05:1.

Process for the work-up of residues of chlorination

A method for preparing hydrogen chloride resulting from chlorination reactions for use in the ethyleneoxichlorination process by reacting the chlorine contained in the hydrogen chloride with ethylene in the gaseous phase in the presence of carrier catalysts based on an iron-free transition metal chloride having an activity profile which increases in the flow direction, while maintaining the space-flow rates relatively high and the residence time of the gas in the reactor short. After discharge of the reaction product from the reactor the product is subjected to partial condensation advantageously performed in several steps.

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Burghausen, Germany

Klaus Haselwarter