Lactams, in particular ε-caprolactam, are produced by the hydrolytic cyclization of aminonitriles, in particular 6-aminocapronitrile, in the vapor phase in a plurality of adiabatic fixed bed reaction zones arranged in succession wherein at least a portion of the heat of the exothermic reaction
Lactams, in particular ε-caprolactam, are produced by the hydrolytic cyclization of aminonitriles, in particular 6-aminocapronitrile, in the vapor phase in a plurality of adiabatic fixed bed reaction zones arranged in succession wherein at least a portion of the heat of the exothermic reaction is removed between each of the successive reaction zones. Conducting the reaction in such a manner requires less capital for the reactor itself. It has also been found that the product exiting such a reaction system can be directly fed to a distillation unit without the need of additional cooling or storing.
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What is claimed is: 1. A process for preparing ε-caprolactam (CPL) by the hydrolytic cylization of 6-aminocapronitrile (ACN) in the vapor phase, said process comprising: (a) contacting a superheated mixture of 6-aminocapronitrile vapor and steam with a catalyst in a plurality of adiabatic reac
What is claimed is: 1. A process for preparing ε-caprolactam (CPL) by the hydrolytic cylization of 6-aminocapronitrile (ACN) in the vapor phase, said process comprising: (a) contacting a superheated mixture of 6-aminocapronitrile vapor and steam with a catalyst in a plurality of adiabatic reaction zones arranged in succession and containing the catalyst, beginning with a first reaction zone and terminating with a final reaction zone, wherein the superheated vapor mixture is fed into the first reaction zone, and a final reaction product comprising CPL is removed from the final reaction zone, and from each reaction zone prior to the final reaction zone an intermediate reaction product is withdrawn, cooled and then fed into the next reaction zone; and (b) separating the CPL from the final reaction product by distillation. 2. The process of claim 1 wherein the 6-aminocapronitrile in the feed mixture contains about 0 to about 1000 ppm tetrahydroazepine and about 0 to about 1 wt % dimer of 6-aminocapronitrile. 3. The process of claim 1 wherein the molar ratio of water to 6-aminocapronitrile in the feed mixture is in the range of about 1:1 to 10:1. 4. The process of claim 1 wherein cooling of at least one of the intermediate reaction products comprises heat exchange. 5. The process of claim 1 wherein cooling of at least one of the intermediate reaction products comprises addition of a cold shot liquid to at least one of the intermediate reaction products, wherein the cold shot liquid is selected from the group consisting of water, methanol, ethanol, ammonia, 6-aminocapronitrile, CPL, hexamethylene diamine, and mixtures of two or more of these compounds. 6. The process of claim 1, comprising a first adiabatic reaction zone and a final adiabatic reaction zone. 7. The process of claim 1, comprising a first adiabatic reaction zone, a final adiabatic reaction zone and at least 3 successive adiabatic reaction zones. 8. The process of claim 7, comprising at least 8 successive adiabatic reaction zones. 9. The process of claim 1 wherein the feed mixture of 6-aminocapronitrile vapor and steam is made by a process comprising: (a) mixing 6-aminocapronitrile with water; (b) vaporizing the mixture of 6-aminocapronitrile and water; and (c) heating the vaporized 6-aminocapronitrile and water to a temperature in the range of about 220째 C. to about 300째 C. 10. The process of claim 1 further comprising: (a) discontinuing the flow of the feed mixture of 6-aminocapronitrile and water vapor through the first adiabatic reaction zone, the successive adiabatic reaction zones and the final adiabatic reaction zone when less than about 95% of the 6-aminocapronitrile in the feed mixture is converted to CPL in the final reaction product; (b) contacting the catalyst in the first adiabatic reaction zone, the successive adiabatic reaction zones and the final adiabatic reaction zone with steam; and then (c) contacting the catalyst in the first adiabatic reaction zone, the successive adiabatic reaction zones and the final adiabatic reaction zone with a mixture of air and steam. 11. The process of claim 10 wherein in step (b) the catalyst is contacted with steam for about 1 to about 10 hours. 12. The process of claim 11 wherein in step (b) the catalyst is contacted with steam for about 2 to about 5 hours. 13. The process of claim 10 wherein in step (b) the steam is at a temperature of about 270째 C. 14. The process of claim 10 wherein in step (c) the maximum temperature in any of the first adiabatic reaction zone, the successive adiabatic reaction zones and the final adiabatic reaction zone does not exceed about 750째 C. 15. The process of claim 14 wherein in step (c) the maximum temperature in any of the first adiabatic reaction zone, the successive adiabatic reaction zones and the final adiabatic reaction zone is in the range of about 550째 C. to about 700째 C. 16. The process of claim 1, wherein the catalyst comprises a solid acid catalyst. 17. The process of claim 16, wherein the solid acid catalyst is selected from the group consisting of Br첩nsted Acids and Lewis Acids. 18. The process of claim 17, wherein the solid acid catalyst is selected from the group consisting of silica, alumina, titania, silica-alumina, zeolites, montmorillonite, sulfuric acid-silica sulfated zirconia, fluorinated alumina, hydrated sulfate, yttrium triflate and aluminum chloride on silica. 19. The process of claim 18, wherein the solid acid catalyst comprises γ-alumina. 20. The process of claim 1, comprising greater than about 90% conversion of the 6-aminocapronitrile in the feed mixture to CPL. 21. The process of claim 1, wherein the exit temperature of at least one adiabatic reaction zone is at least about 5째 C. higher than the inlet temperature of said adiabatic reaction zone. 22. The process of claim 21, wherein the exit temperature of at least one adiabatic reaction zone is at from about 5째 C. to about 30째 C. higher than the inlet temperature of said adiabatic reaction zone. 23. The process of claim 20, wherein the exit temperature of at least one adiabatic reaction zone is at least about 5째 C. higher than the inlet temperature of said adiabatic reaction zone. 24. The process of claim 23, wherein the exit temperature of at least one adiabatic reaction zone is at from about 5째 C. to about 30째 C. higher than the inlet temperature of said adiabatic reaction zone.
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이 특허에 인용된 특허 (3)
Matthias Eiermann DE; Thomas Narbeshuber DE, Method for producing lactams.
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