Abstract: 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.

Abstract: A process is provided for the hydrogenation of chloromethanes of the formula CH.sub.n Cl.sub.m, where n=0 to 3 and m=4-n, with hydrogen at a temperature of 150.degree. to 250.degree. C. and under an absolute pressure of 1 to 10 bar, by means of a supported catalyst comprising an activated charcoal support with a BET surface area of more than 500 m.sup.2 /g, 0.5 to 20% by weight of copper in elemental or chemically bonded form and 0.01 to 1.0% by weight of rhodium or palladium in elemental or chemically bonded form, and with 0.1 to 10.0% by weight of a water-soluble phosphonium halide.

Abstract: 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.

Abstract: A carrier catalyst containing copper and alkali ions on an annular carrier of surface-active material is defined by the dimensions of the carrier body and the porosity of the finished catalyst. Its total pore volume is 0.6-1.0 ml/g, pores smaller than 4 nm diameter are not present, pores of 8-20 nm diameter constitute at least 80% of the total pore volume and the remainder consists of macropores with a diameter greater than 20 nm (i.e., up to 200 nanometers). The catalyst is suitable for the production of 1,2-dichloroethane by means of the oxychlorination of ethylene.

Abstract: The use of hitherto known supported catalysts in chlorination processes and oxychlorination processes leads to high pressure drops and to the formation of hot spot temperatures in the reactor. When honeycomb monolithic catalyst supports provided with a multiplicity of channels open at both ends and parallel to the longitudinal axis are used, both the heat dissipation is improved and the pressure drops across the reactor are lowered drastically. This leads ultimately to an increase in the selectivity of the reaction and to a minimization of the combustion rate.

Abstract: 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.

Abstract: The invention is a multi-stage process for purifying hydrogen chloride containing acetylene and ethylene, from pyrolysis of 1,2-dichloroethane to provide highly pure hydrogen chloride for use in the preparation of silicon compounds. In the first stage, unsaturated by-products are chlorinated by reaction with an excess of chlorine gas. In the second stage, the unreacted chlorine gas remaining in the hydrogen chloride is reacted with an excess of defined olefins or chloroolefins and the hydrogen chloride is separated from the chlorination products and the excess olefins or chloroolefins by low-temperature rectification under pressure.

Abstract: In a process for the purification of hydrogen chloride from the pyrolysis of 1,2-dichloroethane, optionally after a preceding step of acetylene removal by selective hydrogenation under specific conditions followed by rectification of the resulting mixture to obtain hydrogen chloride containing at most 5 ppm of unsaturated hydrocarbons and at most 5 ppm of chlorinated hydrocarbons.

Abstract: 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.

Abstract: 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.

Abstract: In a process for preparation of 1,2-dichloroethane by chlorination of ethylene-containing reaction vent gases from the oxychlorination of ethylene in the presence of a catalyst carrier impregnated with metal compounds wherein the waste from the oxychlorination stage are chlorinated, the improvement comprising preheating the ethylene-containing waste gases to at least 50.degree. C. and then chlorinating the ethylene at 100.degree. to 300.degree. C. at a pressure of 1 to 7 bar with a space velocity of 100 to 5000 h.sup.-1 related to standard conditions in the presence of at least one metal compound selected from the group consisting of chlorides and oxides of manganese, nickel and cobalt supported on a catalyst carrier with reduced formation of oxychlorinated by-products.

Abstract: 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.

Abstract: In a method of recovering heat from flue gas resulting from the combustion of chlorinated organic compounds at 900.degree. to 1300.degree. C. at a pressure of 0.9 to 1.5 bar absolute whereby the flue gas is cooled with the recovery of heat and hydrogen chloride is processed, the improvement comprising (a) cooling the flue gas in a first step to a temperature of 250.degree. to 350.degree. C. with a contact time of 0.05 to 0.15 seconds, (b) cooling the flue gas in a second step to a minimum of 140.degree. C. with a contact time of 1.3 to 2.0 seconds, the cooling medium in both stages being water flowing at an initial temperature of 100.degree. to 140.degree. C. in step (b) counter to the flue gas flow direction and added to cooling stage (a) at a temperature of 200.degree. to 220.degree. C. and (c) cooling the flue gas in a third stage to its dew point and scrubbing it with water to recover the hydrogen chloride therein in solution.

Abstract: 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.

Abstract: 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.

Abstract: 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.

Abstract: An improved process for the removal of acetylene from a hydrogen chloride stream in which the acetylene is converted to vinyl chloride by contact with a hydrochlorination catalyst, the improvement comprising, prior to contacting the stream with the hydrochlorination catalyst, contacting said stream with a catalyst comprising a noble metal, preferably of the platinum group, or salt or oxide thereof, supported or unsupported, at a temperature of between about 50.degree. and about 200.degree. C. and a pressure between about 8 and about 20 bar absolute.

Abstract: The invention relates to a process for the manufacture of unsaturated carboxylic acid esters by the reaction of olefins or cyclo-olefins with oxygen and carboxylic acids in the gaseous phase, in the presence of a catalyst which contains elements of the subsidiary group VIII of the periodic system and/or compounds thereof, and an alkali metal acetate, at temperatures of from 100.degree. to 250.degree. C. and pressures of from 0.5 to 21 bar absolute, wherein from 1 to 8000 parts per million (by weight), calculated on the carboxylic acid used, of organic chlorine compounds are added to the reaction mixture.

Abstract: The invention is a process for the purification of hydrogen chloride formed during the thermal cracking of 1,2-dichloroethane, by hydrogenating the acetylene impurities with excess hydrogen, at pressures of from 8 to 20 bar absolute and at temperatures of from 120.degree. to 180.degree. C., using platinum or palladium supported catalysts, wherein, according to the invention, carrier materials having a specific surface area of not more than 5 m.sup.2 /g are used, the hydrogen excess used is a function of the acetylene content, the gas mixture, after reaching a temperature of approximately 70.degree. C., is permitted a dwell time of not more than 0.8 second before it enters the catalyst, and the temperature, pressure and volume flow rates are dependent on one another within narrow limits.The purified hydrogen chloride is used for oxychlorination.

Abstract: In the chlorination of ethylene in the liquid phase, an excess stoichiometric amount of chlorine is normally used in order to achieve as complete as possible a conversion of the ethylene. Part of the excess chlorine reacts by substitution and thereby reduces the yield of desired 1,2-dichloroethane. The unreacted excess chlorine therefore has laboriously to be removed in subsequent reaction steps. As a result of the method according to the invention to limit the chlorine excess to less than 600 ppm by weight in the reaction cycle, these disadvantages can be obviated. The constant compliance with such a low chlorine excess without fluctuations is rendered possible in industrial operation by the arrangement according to the invention for the continuous recording of the chlorine concentration, even in the presence of catalysts.