Title of Invention	METHOD FOR THE CONTINUOUS PRODUCTION OF METHYL MERCAPTAN
Abstract	The invention relates to a method for the continuous production of methyl mercaptan by reacting an educt gas mixture comprising methanol and hydrogen sulfide in the gas phase at a reaction temperature ranging from 200 to 600?C and an operating pressure of 1.5 to 40 bar on a catalyst in a multi-bed reactor.

Full Text

WO 2006/108737 PCT/EP2006/060403 METHOD FOR THE CONTINUOUS PRODUCTION OF METHYL MERCAPTAN The invention relates to a process for the continuous production of methyl mercaptan by reacting a starting gas mixture of methanol and hydrogen sulphide in the gas phase at a reaction temperature of between 200 and 600°C and an operating pressure o£ 1.5 to 40 bar on a catalyst m a multi-bed reactor. Methyl mercaptan is an industrially important intermediate for the synthesis of methionine and for the production of dimethyl sulphoxide and dimethyl sulphone. Methyl mercaptan is mainly produced from methanol and hydrogen sulphide by reaction on a catalyst consisting of an alumina support and transition metal oxides and basic promoters. The synthesis of the mercaptan is usually carried out in the gas phase at temperatures between 300 and 500°C and at pressures between 1 and 2 5 bar. The reaction of hydrogen sulphide and methanol to give methyl mercaptan is an exothermic process. DE-C 196 54 515 describes, for example, a process for the production of methyl mercaptan in a tube bundle reactor, in which the liberated heat of reaction is dissipated by means of a salt melt and is then utilized indirectly by means of heat exchangers for the evaporation of methanol. In addition to the methyl mercaptan formed and water, the product gas mixture contains the unreacted starting substances methanol and hydrogen sulphide and, as by- products, dimethyl sulphide and dimethyl ether, and in small amounts also polysulphides (dimethyl disulphide). In accordance with the reaction, inert gases such as, for example, carbon monoxide, carbon dioxide, nitrogen and hydrogen are also present in the product gas. The methyl mercaptan formed, as explained in DE 17 68 82 6, is separated off from the product gas mixture in a number of distillation and scrubbing columns at temperatures between 10 and 140°C. WO 2006/108737 2 PCT/EP2006/060403 The reaction according to GB 14 17 532 can be carried out in a fixed bed reactor containing a number of catalyst beds or in a number of consecutive reactors. Methyl mercaptan is prepared here by the reaction of a mixture of methanol with hydrogen sulphide in a molar ratio of 1.10 : 1 and 2 t 5, i If both reaction components being fed to the reactor separately. According to FR 24 77 538, for the production of methyl mercaptan fresh hydrogen, sulphide gas is compressed to 11 bar in a compressor. Afterwards, cycle gas led back from the process, which contains hydrogen sulphide, dimethyl sulphide, methanol and small amounts of methyl mercaptan, is mixed with the compressed hydrogen sulphide for the formation of the starting gas mixture and this is heated to 510°C. Before entry into the first of up to 10 reactors connected in series, the washing agent cycle stream, which contains methanol and dimethyl sulphide, is admixed to the starting gas mixture, whereby the reaction entry temperature falls to 450°C. Before the second and the following reactors, further methanol, partly as a liquid and partly as a gas, is injected into the gas stream. DE-C 11 34 368 relates to the use of a tube bundle reactor for the production of methyl mercaptan. The reactor consists of a cylindrical container, in which the catalyst tubes are arranged parallel to one another. The catalyst tubes are welded below and above with tube cover plates, as in tube bundle heat exchangers, the intermediate spaces between the tubes being filled with heat-conducting fluid. Each catalyst tubes is provided at its lower end with a screen, which carries the particulate catalyst. DE 196 54 515 relates to a process for the production of methyl mercaptan, in which the energy needed for the evaporation of the methanol is partly introduced by utilization of the heat of compression of the hydrogen sulphide gas and by the heat content of the product gas leaving the reactor. The heat of reaction is utilized here WO 2006/108737 3 PCT/EP2006/060403 in order to heat the starting gas mixture to the reaction temperature with the aid of an external gas heater. The economy of the overall process depends crucially on the reaction of the starting gas mixture in a suitable pressure reactor and the preparation of this gas mixture. For example, large electrical powers are needed for the operation of the compressors and of the heating and cooling circuits. Further, expensive changes of catalyst in tube bundle reactors on account of long stoppage times represent a time and cost factor which is not to be neglected. The object of the invention is the provision of an economic process for the production of methyl mercaptan. The invention relates to a process for the continuous catalysed production of methyl mercaptan by reaction of methanol and hydrogen sulphide in the gas phase at a temperature of 200 to 600°C, in particular 250 to 500°C and a pressure of 1.5 to 40 bar, where a) the total amount of catalyst is distributed equally or unequally to at least two, preferably at least three, zones which are separate from one another, b) the first of these zones is supplied with a gaseous mixture comprising methanol and hydrogen sulphide (starting gas), c) between the first, the second and optionally the further zones, methanol is fed in in liquid and/or gaseous form, and d) the methyl mercaptan formed is separated off, the overall molar ratio of the amounts of hydrogen sulphide and methanol employed amounting to 1:1 to 10:1, preferably 1:1 to 5:1, particularly preferably 1.1:1 to 3:1. WO 2006/108737 4 PCT/EP2006/060403 The gaseous mixture of hydrogen sulphide and methanol (starting gas) contains these two compounds in a molar ratio of 1.1:1 to 20:1, preferably 1.1:1 to 10:1, in particular 3:1 to 10:1 and optionally by-products from the reaction and inert gases, if, for example, unreacted components are separated off from the product gas stream together with these compounds and recycled. The use of this starting gas guarantees even in the first catalyst bed thorough mixing of the roactants and a heat of reaction, generated by the high conversion, which is employed for the evaporation of the methanol fed in after the first zone. If, as customary according to the prior art (GB 14 17 532), methanol is fed in even before the first zone, evaporation energy must additionally be supplied. Likewise, the methanol fed in between the zones containing the catalysts can contain sulfur-containing starting materials or products, but consists essentially (in general > 90 mol%) of methanol. Preferably, an operating pressure of 2.5 to 25 bar is set. The compression of the starting gases to the operating pressure is carried out in one or more stages. In the first catalyst-containing zone, the hydrogen sulphide is always present in an excess compared to methanol. The total amounts of the methanol fed in in the starting gas and between the zones are in the ratio from 1:1 to 1:10, preferably 1:2 to 1:7. Preferably, grid reactors are employed which contain 2 to 25 catalyst beds (zones), in particular 3 to 10, preferably 3 to 8. At the same time, also at least two of these reactors can be connected to one another. WO 2006/108737 5 PCT/EP2006/060403 Grid reactors allow the direct metering in of gaseous and liquid methanol, hydrogen sulphide or a starting gas mixture containing, inter alia, methanol and hydrogen sulphide between the catalyst beds (grids), where the heat of reaction liberated in the grids is utilized directly for the evaporation of the methanol, and the temperature of the gas mixture drops before entry into the next grid. As a Result of this concept, powerful methanol evaporators can be dispensed with. The economy of the overall process is also made possible in comparison with tube bundle reactors (with thousands of individual tubes to be filled and emptied), by more rapid modular catalyst exchanges in the grids. Thus the catalyst of each grid can be exchanged separately. This is particularly advantageous if the deactivation of the catalyst, as in the synthesis of methyl mercaptan, is dependent on the concentrations of the reactants and thus on the site or reaction progress. Furthermore, the use of various catalysts in a reactor is facilitated thereby. As a result of the use of the grid reactor, especially in reactions with very strong evolution of heat, such as, for example, the synthesis of methyl mercaptan from methanol and hydrogen sulphide by means of catalysts customary for the process, excellent temperature control is possible by choice of the grid size and the amount of injected liquid. By this means, in the synthesis of methyl mercaptan, high excess temperatures, which lead to decreased yields and to an increased deactivation of the catalyst, can be avoided. Figure 1 and Figure 2 serve for the further explanation of the process using the preferably employed grid reactor. Figure 1 shows a process scheme of the first section of the production process of methyl mercaptan. Figure 2 shows a detail representation of a grid reactor used in this process. WO 2006/108737 6 PCT/EP2006/060403 Figure 1 shows a process scheme for the first section of the methyl mercaptan production, which comprises the starting gas preparation, the reaction in the reactor and the cooling of the product gas mixture. The reaction in the grid reactor 1 is carried out on customary catalysts, preferably on alumina, as a carrier, which are preferably coated with alkali metal tungstate, in particular caesium tungstate. The catalysts are described in the applications WO 2005/021491, DE 10 2004 77 39 and DE 10 2004 061 016. Catalysts of this type are able to react a starting gas mixture having a molar ratio of hydrogen sulphide to methanol of 1.5 : 1 to 10.0 : 1 at an operating pressure of 5-20 bar, a reaction temperature of 280 - 450°C and at a loading with a space rate GHSV of 300-2000 h"1 with a methanol conversion and a selectivity of in each case more than 90 % to give methyl mercaptan. The process according to the invention also allows the preparation of methyl- mercaptan using otherwise customary catalysts. On account of the very active catalysts for the synthesis of methyl mercaptan, which especially contain halide-free alkali metal tungstates, halide-containing alkali metal tungstates or preferably halide-free or -containing caesium tungstates as promoters, an excellent temperature control for the operation of these catalysts at the yield optimum, without an increased deactivation of the catalyst having to be feared, is necessary. This is made possible when using these and other customary catalysts and carrying out according to the invention the synthesis in a grid reactor. The starting gas mixture 2 consisting of methanol vapour, hydrogen sulphide and optionally further of the above- mentioned components is heated in the gas heater 3 to the reactor entry temperature (pre-temperature) of 100-350°C. The starting gas mixture reaches the grid reactor at this temperature. WO 2006/108737 7 PCT/EP2006/060403 On account of the quantitative proportion of methanol and hydrogen sulphide, the starting gas mixture cannot be confused with a hydrogen sulphide gas which contains small amounts of methanol as a result of recycling. The gas mixture is dispersed uniformly over the catalyst bed of the first reactor grid by means of dispersing devices. For better heat transfer, the catalyst bed of the first reactor grid is optionally covered with a layer of inert, solid packing materials, at least in the area of the entry of the gas stream. Advantageously, for this, for example, packing material spheres of ceramic, silica or alumina are used. The grid reactor in general contains 2 to 25 catalyst beds, advantageously 2 to 10 catalyst beds, preferably 3-8, are accommodated in one apparatus. Between the grids, liquid or optionally gaseous methanol, optionally also hydrogen sulphide or the starting gas mixture 2 is metered into the process. Methanol is preferably fed to the process in liquid form between all grids or some of the grids. At the same time, the heat of reaction which is released in the grid situated before the injection site is utilized for the evaporation of the methanol and for the control of the temperature in the strongly exothermic reaction. A lengthening of the bed length of the catalyst grids or an increase in the amount of catalyst from the first to the last grid (zone) in the flow direction has proved advantageous. Optionally, no methanol is fed in before the last grid. Between the catalyst grids are optionally situated devices, such as, for example, static mixers, ordered or disordered packings, which make possible a turbulent flow course and a uniform dispersion and mixing of the reactants. Preferably, the starting gas mixture optionally metered in between the catalyst grids and/or the liquid methanol is dispersed radially, tangentially or zone-wise over the catalyst bed WO 2006/108737 8 PCT/EP2006/060403 by means of a gas disperser, so that a uniform turbulent flow distribution and complete mixing of the reactants results. The mixing of the reactants can be improved by optional introduction of inert layers of packing materials. The catalyst grids are advantageously designed as catalyst beds having radial, square or polygonal geometry, other geometries also being possible. The grids can individually be filled with catalyst or emptied. Preferably, they are designed such that they can be removed from the reactor in modular form. Alternatively, in each case a detachable or undetachable connection or opening in the reactor wall can be utilized for the simple exchange of the catalyst. In a further embodiment of the invention, the grids are filled with at least two different catalysts. The dependence of the local yield and local selectivity, especially in the synthesis of methyl mercaptan, is thus taken into account as a function of the concentrations of the reactants and thus the progress of the reaction. For example, it is advantageous in the synthesis of methyl mercaptan to fill the last grid with a very active catalyst if a complete conversion of methanol is desired. If the reaction is to be operated with respect to maximum selectivity, a less active, but for this very selective catalyst can be employed in the last grid. The grid reactor thus makes possible, by means of simple, site-dependent filling, flexibility in the production of methyl mercaptan. The product gas mixture 4 leaves the reactor at the reaction temperature of the last grid. Its heat content can be utilized in the heat exchanger 5 for the evaporation of methanol or for the production of steam etc. In this process, the product gas mixture cools to approximately 150°C and is fed to the second process section as a volume flow 6. The separation of the product gas mixture into its WO 2006/108737 9 PCT/EP2006/060403 components is performed in the second process step of the methyl mercaptan production. The separation can be carried out according to various, known processes. A particularly- advantageous separation of the product gas mixture is described in German patent specification DE-C 196 54 516. The leading back of the hydrogen sulphide separated off in the second process step as a cycle gas stream is important for the economy of the process. The same applies for the methanol separated off from the product gas mixture and not completely consumed in the reaction in the reactor, and for the wash methanol optionally used in the second process step. Fig. 2 shows the preferred embodiment of the reactor, according to Claim 1. In the reactor 1, n (n = 2-25) catalyst beds are accommodated. Preferably, 3-10 catalyst beds (grids) are used. The starting gas mixture 2 enters through the distributor space 7 into the first catalyst bed 8. This first catalyst bed is optionally first covered with a packing of inert materials in the flow direction of the starting gas. For example, alumina spheres or ceramic Raschig rings are used as inert materials. Subsequent to the inert layer is situated the catalyst packing. As a result of the strongly exothermic formation of methyl- mercaptan, in the course of this the temperature in the adiabatic grid increases greatly. After leaving the first grid, the gas mixture is enriched in the distributor space 9 with liquid methanol 10, hydrogen sulphide 10 or optionally the starting gas mixture 2. As a result of the heat of reaction of the first grid, the liquid methanol evaporates without further supply of heat. By this means, the temperature of the gas mixture drops. The gas mixture subsequently flows from the distributor space 9 into the second catalyst bed 11, devices in the distributor space 9 providing for a turbulent flow and a complete mixing of the reactants, which is distributed uniformly to the entire surface of the second catalyst bed. The supply of liquid WO 2006/108737 10 PCT/EP2006/060403 methanol or optionally hydrogen sulphide or starting gas mixture takes place analogously at n-1, preferably n-2, injection sites between the following catalyst beds of the grid reactor. Optionally, a supply of liquid methanol, hydrogen sulphide or starting gas mixture before the last catalyst bed at the injection site 12 can be dispensed with in order to obtain a complete conversion of methanol in the reaction. After leaving the grid reactor, the reacted gas mixture is fed to further processing via the collecting space 13 as a product gas stream 4. Thus, the temperature of a strongly exothermic reaction can be excellently controlled in only one reaction apparatus including an integrated direct heat exchange without additional heat carrier media such as salt melts or steam. The process scheme shown in Fig. 1 contains the necessary components for carrying out the process according to the invention. WO 2006/108737 11 PCT/EP2006/060403 Patent claims 1. Process for the continuous catalysed production of methyl mercaptan by reaction of methanol and hydrogen sulphide in the gas phase at a temperature of 2 00 to 600°C and a pressure of 1.5 to 40 bar, where a) the total amount of the catalyst is distributed to at least two zones which are separate from one another, b) the first of these zones is supplied with a gaseous mixture comprising methanol and hydrogen sulphide, c) between the first, the second and optionally the further zones methanol is fed in in liquid and/or gaseous form, and d) the methyl mercaptan formed is separated off, e) the total molar ratio of the amounts of hydrogen sulphide and methanol employed amounting to 1:1 to 10:1, preferably 1:1 to 5:1. 2. Process according to Claim 1, characterized in that a grid reactor having 2 to 25 catalyst beds, preferably 3 to 10 catalyst beds, is employed. 3. Process according to Claim 1 or 2, characterized in that the catalyst packings in the zones are covered with a layer of the packings of inert materials. 4. Process according to Claim 3, characterized in that the first catalyst zone in the flow direction and optionally the last zone are completely or partly coated with an inert material. WO 2006/108737 12 PCT/EP2006/060403 5. Process according to Claims 1 to 4, characterized in that at least two different catalysts are employed in the zones. 6. Process according to Claims 1 to 5, characterized in that the amount of catalyst between the zones varies, in particular increases in the flow direction. 7. Process according to Claims 1 to 6, characterized in that the total amount of hydrogen sulphide employed is employed as a gaseous mixture of methanol and hydrogen sulphide. 8. Process according to Claims 1 to 6, characterized in that hydrogen sulphide or starting gas is fed into the intermediate space between one or more of the first and second or further zones. 9. Process according to Claim 1 or 2, characterized in that the molar ratio of hydrogen sulphide to methanol in the starting gas is 1.1:1 to 20:1, preferably 1.1:1 to 10:1, in particular 3:1 to 10:1. 10. Process according to Claim 1 or 2, characterized in that the methanol is fed into the intermediate spaces between the zones in equal amounts. 11. Process according to Claim 1 or 2, characterized in that the methanol is fed into the intermediate spaces between the zones in unequal amounts. 12. Process according to Claim 1 or 2, characterized in that the last catalyst-containing zone is not supplied with methanol. 13. Process according to Claims 2 to 12, characterized in that the catalyst beds are flowed through in variable directions with methanol and hydrogen sulphide. WO 2006/108737 13 PCT/EP2006/060403 14. Process according to Claims 1 to 13, characterized in that the catalysts employed are alkali metal tungstates or halide-containing alkali metal tungstates. 15. Process according to Claim 14, characterized in that halide-free or halide-containing caesium tungstates are employed. 16. Process according to Claims 1 to 15, characterized in that the reaction mixture is in each case completely mixed between the zones by introduction of inert packing materials and/or devices which make possible a turbulent flow course and a uniform distribution and mixing of the reactants. 17. Process according to Claims 1 to 16, characterized in that the catalyst grids are designed as catalyst beds having radial, square or polygonal geometry and the grids can be individually filled with catalyst or emptied, their design optionally being such that they can be removed from the reactor in modular form. 18. Process according to Claims 1 to 17, characterized in that in each case at least one detachable or undetachable connection or opening in the reactor wall is utilized for the simple exchange of the catalyst in the individual grids. The invention relates to a method for the continuous production of methyl mercaptan by reacting as educt gas mixture comprising methanol and hydrogen sulfide in the gas phase at a reaction temperature ranging from 200 to 600?C and an operating pressure of 1.5 to 40 bar on a catalyst in a multi-bed reactor.

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03802-kolnp-2007-abstract.pdf

03802-kolnp-2007-claims.pdf

03802-kolnp-2007-correspondence others 1.1.pdf

03802-kolnp-2007-correspondence others.pdf

03802-kolnp-2007-description complete.pdf

03802-kolnp-2007-drawings.pdf

03802-kolnp-2007-form 1.pdf

03802-kolnp-2007-form 2.pdf

03802-kolnp-2007-form 3.pdf

03802-kolnp-2007-form 5.pdf

03802-kolnp-2007-gpa.pdf

03802-kolnp-2007-international exm report.pdf

03802-kolnp-2007-international publication.pdf

03802-kolnp-2007-international search report 1.1.pdf

03802-kolnp-2007-international search report.pdf

03802-kolnp-2007-pct priority document notification.pdf

03802-kolnp-2007-pct request form.pdf

03802-kolnp-2007-translated copy of priority document.pdf

3802-KOLNP-2007-(14-08-2012)-ABSTRACT.pdf

3802-KOLNP-2007-(14-08-2012)-AMANDED CLAIMS.pdf

3802-KOLNP-2007-(14-08-2012)-ANNEXURE TO FORM 3.pdf

3802-KOLNP-2007-(14-08-2012)-DESCRIPTION (COMPLETE).pdf

3802-KOLNP-2007-(14-08-2012)-DRAWINGS.pdf

3802-KOLNP-2007-(14-08-2012)-EXAMINATION REPORT REPLY RECEIVED.pdf

3802-KOLNP-2007-(14-08-2012)-FORM-1.pdf

3802-KOLNP-2007-(14-08-2012)-FORM-2.pdf

3802-KOLNP-2007-(14-08-2012)-FORM-3.pdf

3802-KOLNP-2007-(14-08-2012)-FORM-5.pdf

3802-KOLNP-2007-(14-08-2012)-OTHERS.pdf

3802-KOLNP-2007-(21-08-2012)-CORRESPONDENCE.pdf

3802-KOLNP-2007-(21-08-2012)-OTHERS.pdf

3802-KOLNP-2007-(21-08-2012)-PETITION UNDER RULE 137.pdf

3802-KOLNP-2007-(28-10-2011)-CORRESPONDENCE.pdf

3802-KOLNP-2007-(28-10-2011)-FORM 3.pdf

3802-KOLNP-2007-CORRESPONDENCE OTHERS 1.2.pdf

3802-kolnp-2007-correspondence.pdf

3802-kolnp-2007-form 13.1.pdf

3802-kolnp-2007-form 13.pdf

3802-KOLNP-2007-INTERNATIONAL EXM REPORT 1.1.pdf

3802-KOLNP-2007-INTERNATIONAL SEARCH REPORT 1.2.pdf

3802-kolnp-2007-others.pdf

3802-kolnp-2007-p.a.pdf

3802-KOLNP-2007-PCT REQUEST FORM 1.1.pdf

3802-KOLNP-2007-PETITION UNDER RULE 134.pdf

3802-KOLNP-2007-REPLY TO EXAMINATION REPORT.pdf

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