3,426,085 United States Patent Office Patented Feb. 4, 1969 1. 2 whereas in the process of addition of hypochlorous acid 3,426,085 PROCESS FOR THE MANUFACTURE OF to ethylene considerably better yields are obtained. ETHYLENE CHLOROHYDREN The present invention provides a process for the manu Ginther Mau and Lothar Hörnig, Frankfurt am Main, facture of ethylene chlorohydrin, which comprises re Germany, assignors to Farbwerke Hoechst Aktiengesel acting ethylene, oxygen and hydrogen chloride in the schaft vormals Meister Lucius & Bruning, Frankfurt am presence of water in the liquid or gaseous phase using Main, Germany, a corporation of Germany a catalyst containing tellurium and/or tellurium com No Drawing. Filed Dec. 1, 1966, Ser. No. 598,218 pounds. Claims priority, application Germany, Dec. 24, 1965, Working in the liquid phase is preferred in many cases. F 47,997 Solutions of readily accessible tellurium compounds are U.S. Cl. 260-634 6 Claims 0 then used, for example tellurium dioxide, tellurium tetra Int. C. C07c 29/04 chloride or telluric acid. It is also possible to use solutions of alkali metal tellurites or tellurates, tellurium sulfate or tellurium nitrate. As solvent aqueous hydrochloric ABSTRACT OF THE DISCLOSURE 15 acid is preferred. It may also be used in admixture with A process has been provided for producing ethylene organic solvents, advantageously organic solvents mis chlorohydrin which comprises reacting, at a temperature cible with water, for example ethanol, glycol and other from about 50° C. to about 300° C. and a pressure from alcohols. To reduce the solubility of the reaction prod about 1 to about 50 atmospheres, ethylene, oxygen, and ucts, especially of ethylene chlorohydrin, the catalyst hydrogen chloride, in the presence of water, the molar 20 Solution may contain dissolved salts, for example alkali ratio of ethylene to oxygen being from 2:1 to 20:1, and metal chlorides. Water to ethylene greater than 1:1, said reaction being To perform the reaction of ethylene and oxygen in the carried out in the presence of a tellurium catalyst selected catalyst Solution a mixture of both gases can be used. from the group consisting of elementary tellurium, telluri Alternatively, the ethylene can be first reacted with the um dioxide, tellurium tetrachloride, telluric acid, alkali 25 catalyst solution, whereby the tellurium compound con metal tellurites, alkali metal tellurates, tellurium sulfate, tained in the catalyst solution is reduced to elementary and tellurium nitrate, and recovering ethylene chlorohy tellurium, oxygen can then be introduced into the solu drin. The process can be carried out in an aqueous phase tion to re-oxidize the elementary tellurium. In either case as well as in a gaseous phase. If carried out in an aqueous hydrogen chloride and water are added to the system in phase, the concentration of hydrogen chloride in the 30 the same measure as they are consumed, suitably in the aqueous catalyst solution is from 10% to 35% by weight. form of aqueous hydrochloric acid. Further, gaseous hydrogen chloride may also be used in More particularly, the process of the invention is car the aqueous process. When the process is carried out in ried out as follows: ethylene and oxygen are blown into a gaseous phase, the tellurium catalyst is deposited on a reactor filled with catalyst solution containing water a solid carrier and water is used in the form of steam. and hydrogen chloride. As reactor a vessel with stirrer, a In another novel aspect of this invention, the ethylene bubble column, a flow tube, a scrubbing tower or an air may first be reacted with the catalyst solution and then the lift pump may be used. It is expedient to adjust tempera catalyst solution is reoxidized with oxygen in a separate ture and pressure to such a value that the ethylene chloro reaction vessel. hydrin formed can escape as vapor. When the process is 40 carried out at atmospheric pressure, a reaction tempera amma ture of about 95 to 100° C. is suitable. It is likewise The present invention relates to a process for the manu possible, however, to first leave the ethylene chlorohydrin facture of ethylene chlorohydrin, wherein ethylene, oxy in the reaction solution and to remove it in another gen and hydrogen chloride are reacted in the presence of place by distilling the total amount or part of the reac water in the liquid or gaseous phase using catalysts con tion Solution. taining tellurium and/or tellurium compounds. Ethylene and oxygen can be introduced separately from Ethylene chlorohydrin is produced on an industrial one another as regards time and place. In the latter case scale from ethylene and hypochlorous acid. It constitutes a system of two series-connected reactors can be used an intermediate product in the production of glycol ob through which the catalyst is conducted. A preferred em tained either by alkaline saponification of ethylene chloro bodiment consists in that ethylene is first reacted with hydrin or by separation of hydrogen chloride with forma the catalyst solution and the catalyst is then re-oxidized tion of ethylene oxide and subsequent hydration of the with oxygen either subsequently or in a separate vessel. latter. In this latter process ethylene oxide may be con The tellurium content of the catalyst solution in the sidered a derivative of ethylene chlorohydrin. Presently, form of tellurium compounds is suitably in the range of ethylene oxide is frequently produced by direct oxidation 55 from 10 to 200 grams of tellurium per liter of catalyst of ethylene in the presence of silver catalysts. Besides the solution. It is likewise possible, however, to operate with further working up of ethylene oxide to glycol, the addi a solution having a concentration of 1 gram of tellurium tion of hydrogen chloride to ethylene oxide with forma per liter. With higher concentrations of tellurium, for tion of ethylene chlorohydrin is industrially important so example, 500 grams per liter of solution the process can that in this case ethylene chlorohydrin can inversely be 60 also be carried out with advantage, especially when ethyl considered a derivative of ethylene oxide. ene and oxygen are reacted with the catalyst separately The direct oxidation of ethylene to ethylene oxide has with regard to time or space, that is to say one after not been able to supersede completely the older process the other. of the addition of hypochlorous acid to ethylene, although The reaction is suitably carried out at a temperature in the older process for each mol of ethylene chlorohydrin 65 in the range of from 50 to 250 C. With temperatures one mol of elementary chlorine must be used and one above 100° C. it is generally necessary to operate under mol of hydrogen chloride and in the further working up pressure. As already mentioned, it is expedient to operate of the ethylene chlorohydrin an additional mol of hydro at a temperature a little below the boiling point of the gen chloride or the equivalent amount of chloride are fresh catalyst solution. The pressure applied is conse necessarily obtained. The drawback of the direct oxida 70 quently in the range of from 1 to 50 and preferably 1 to tion process is that the yield of ethylene oxide, calculated 20 atmospheres. on the ethylene used, amounts to only about 50-60%, In general, the conversion increases with the tempera 3,426,085 3 4. ture, the pressure and the concentration of tellurium in gaseous phase as follows: a gas mixture containing ethyl the catalyst solution. It is not expedient, however, to ene, oxygen, hydrogen chloride and steam is passed operate at too high a temperature since in this case in through a reactor filled with the catalyst. The reactor may creasing amounts of by-products are formed. be designed as a shaft reactor, a bundle of tubes, a fluid The concentration of hydrogen chloride in the aqueous ized bed or a gas lift. The issuing gas mixture is cooled catalyst solution is critical. It is advantageously in the at the end of the reactor and condensed, suitably in stages. range of from 10 to 35% by weight. With lower concen In addition to water, ethylene chlorohydrin is obtained trations lower conversions are obtained whereas higher which is worked up as described above. Unreacted Start concentrations involve lower yields. In the latter case in ing components are suitably reconducted into the reactor. creasing amounts of chlorinated hydrocarbons are formed. The by-products ethanol and ethyl chloride, mentioned The water content of the catalyst solution is preferably O with the process in the liquid phase, as well as aqueous in the range of from 30 to 90 and more preferably 40 to hydrochloric acid may also be recycled into the reaction 80% by weight. The concentrations of hydrogen chloride ZOle. and water in the catalyst solution change owing to con The starting components can be introduced separately sumption and discharged material, if any, and therefore, into the reactor. The reactor may also be provided with the two components are replenished either continuously several inlets for one or several reactants, respectively. or discontinuously. The starting components may contain the inert gases The starting components ethylene and oxygen can be specified above. It is particularly advantageous to use used in admixture with inert gases, for example, ethane, oxygen in the form of air and hydrogen chloride in the methane, nitrogen, noble gases, methyl chloride, carbon 20 form of vapors of aqueous hydrochloric acid. dioxide and the like. The oxygen is preferably used in The concentration of tellurium in elementary or bound the form of air. form in the solid catalyst varies advantageously between In many cases, the conversion of the components used 0.1 and 50% by weight, more advantageously 0.5 and is not quantitative.