• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:

    公开号:SU1318153A3
    申请号:SU802948390
    申请日:1980-07-09
    公开日:1987-06-15
    发明作者:Коморн Ив；Швахофер Гислен
    申请人:Рон-Пуленк Эндюстри (Фирма)；
    IPC主号:
    专利说明:

    eleven
    This invention relates to an improved process for the preparation of / 3-methylthiopropioaldehyde, which is used as an intermediate in the synthesis of methionine.
    The purpose of the invention is to simplify the process.
    The drawing is a process flow diagram.
    The gas stream 1, which comes from the oxidation reactor and contains acrolein, water and acrylic acid as the main condensable products, enters the absorption column A, into which either water or a solvent, for example, tributane phosphate, or a mixture of diphenyl and diphenyl ether is fed through line 2.
    Acrylic acid solution is withdrawn through line 3.
    The gas stream 4 exiting the absorption column A is condensed in one or more capacitors B.
    The liquid mixture 5 leaving the condensation stage and containing mainly water and acrolein is subjected to partial evaporation in apparatus C, i.e. separation into two phases: an aqueous phase not containing more than acrolein 6, and a gas phase containing all acrolein 7 that is recycled to the gas flow A leaving the first stage of absorption of acreic acid before it enters through conduit 8 into one or several condensers B .
    Partial evaporation of the resulting liquid mixture is carried out either in a single evaporation apparatus, or in an extraction distillation apparatus, or in an apparatus for distilling light fractions by steam or in an evaporator with a thin layer — rotating or non-rotating.
    The gas mixture 9, coming out of one or more capacitors B, is introduced into the lower part of the absorption column D, at the head of which is fed 3-methylthiopropionic aldehyde 10. Mixture 11 leaving this column (acrolein, absorbed / 3-me tiltiopropionovym aldehyde) enters the reactor. E, where methyl mercaptan 12 and the catalyst are fed.
    A part of the obtained α-methylthiropropionic aldehyde is taken through conduit 13, another part 10 through 5
    8153 2
    is recycled to the head of the absorption column D, from where residual gases are removed through line 14.
    Example 1. Gaseous effluent 1, leaving after the reaction of catalytic oxidation of propylene with air and the presence of water, has the following composition, mol: O Inert gases 547
    Water395
    Acrolein 49,6
    Acrylic acid 6
    Acetaldehyde and others. 2.4 5 The effluent, which is at a temperature of 350 ° C, enters the absorption column A fed through pipe 2 with tributyl phosphate at. A solution of acrylic acid and tributyl phosphate containing traces of water and acrolein comes out of the bottom of the column via line 3.
    From the top of the column comes out. gas stream 4 at 80 C, having the following composition:
    Inert gases 547
    Water392
    Acrolein 49.2
    Acrylic acid0.06
    Acetaldehyde
    and others.2
    and it enters the condenser B, where it is cooled before and the two streams that form are divided into 5: a liquid stream and a gaseous stream. I
    Liquid stream 5 is sent to apparatus C, which is a distillation column 0, fed through an upper plate which is at 83 ° C under a pressure of 1.5 abs. atm After the partial evaporation process, two streams form in the column: on one 5 side a liquid stream 6 containing traces of acrolein, acrylic acid, etc., on the other side a gas stream 7 that recycles condenser B through line 8. Q Gas mixture 9 is injected in the absorption column D fed from above with methyl thiopropionic aldehyde 10. Acrolein absorbed in the s-methylthio-propionic aldehyde 11 is introduced into the reactor B, where the catalyst (triethylamine), 0.05% of the reaction mass and methyl mercaptan 12 are also introduced ( molar flow rate 49.3 m ol). At the exit of the reactor, through line 13,
    0
    313181534
    part of the obtained / J-methylthiolones is poured, from where, via line 1A of the propionic aldepdz, residual gas flows in this way. so that the initial redundant part 14
    was recycled after cooling. The molar flow rates for the various pipes at a temperature of –10 ° C on top of both are given in Table. one.
    Table 1
    Inert gases 547 547
    Water Acrolein
    Acrylic acid
    Acetaldehyde and others.
     -Methyl-thiopropionic aldehyde
    395392
    .49,649,2
    60.06
    2.42
    547 - - - 547 547 398 396 6 390 2 - 59.9 10.75 10.7 0.05 49.15 0, 06 0.06
    0.06
    2.2 0.7 0.2 0.5 1.5 1.5
    0.15
    At the same time, 99.5% of acrolein exiting through pipe 4 is collected in vaporous form in pipe 9 into the gas mixture introduced into the absorption column D.
    Example 2 (comparative). It works in the same way as in example 1, but without the stage of partial evaporation in apparatus C. In this case, the sidc mixture leaving condenser B is directed to the recovery of acrolein via an additional pipeline. The gas mixture 9 is sent to the reaction stage with the mercaptan.
    The composition of these two mixtures are given in table. 2
    table 2
    VNIIPI Order 2439/57 Edition 372
    Random polygons pr-tie, Uzhgorod, st. Project, 4
    0.06
    0.4
    0.15 48.7
    G Continued table 2

    Comparison of the composition of the pipe 9 of the table. 1 (previous level of technology) and the composition of the pipe 9 of the table. 2 clearly shows the advantage of the proposed method (42 moles of gaseous acrolein are presented in stream 10 of the prior art, while 49.2 moles of them are presented in stream 10 of the invention with the same amount of acrolein being in pipe 4).
    Subscription
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PRODUCING / P-METHYLTIOPRO PIONIC ALDEHYDE, comprising the first stage of the separation of acrylic acid from the gas stream coming from the catalytic oxidation of propylene and containing acrolein, acrylic acid and water, absorption by water or solvent, the second stage of water removal by condensation of the gas-air stream the first stage, and the third stage of the interaction of acrolein contained in the gas stream leaving after the second stage in p-Metippropionic aldehyde with methyl mercaptan in the presence of vii as a catalyst of an organic base at 10-50 ° C, characterized in that, in order to simplify the process, the removal of water from the gas stream in the second stage is carried out by evaporation at a temperature of 83-100 ° C and a pressure of 1-1.5 bar, s subsequent recirculation of the resulting gas phase containing acrolein into the gas stream leaving after the first stage, before the second stage.
    »SU <„ 1318153 A 5
    1 '13
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    同族专利:
    公开号 | 公开日
    JPS578098B2|1982-02-15|
    ES8104216A1|1981-04-16|
    CA1138896A|1983-01-04|
    FR2460925B1|1981-08-14|
    BR8004260A|1981-01-27|
    FR2460925A1|1981-01-30|
    DE3060131D1|1982-02-18|
    EP0022697A1|1981-01-21|
    US4319047A|1982-03-09|
    EP0022697B1|1981-12-30|
    ES493224A0|1981-04-16|
    JPS5653648A|1981-05-13|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2626282A|1949-10-05|1953-01-20|Standard Oil Dev Co|Vapor phase production of betamethylmercaptopropionaldehyde|
    FR1520328A|1966-04-25|1968-04-05|Sumitomo Chemical Co|Two-step production process for beta-methylmercaptopropionaldehyde|
    FR1526355A|1966-04-30|1968-05-24|Sumitomo Chemical Co|Manufacturing process of beta-methylmercaptopropionaldehyde|
    ES357862A1|1967-10-13|1970-04-01|Glanzstoff Ag|Process for the production of beta-methylmercaptopropionaldehyde|
    FR2314917B1|1975-06-20|1977-12-02|Rhone Poulenc Ind|DE3010429A1|1980-03-19|1981-09-24|Bayer Ag, 5090 Leverkusen|METHOD FOR PRODUCING SYNTHESIS RUBBER MATERIALS, THEIR USE AS ADHESIVE ADHESIVE RAW MATERIAL IN THE PRODUCTION OF ADHESIVE ADHESIVES AND ADHESIVE ADHESIVES|
    US4777289A|1986-05-08|1988-10-11|Monsanto Company|Process for the preparation of alkylthioalkanoate salts|
    US4944853A|1989-09-11|1990-07-31|Pennwalt Corporation|Photochemical preparation of 3- aldehydes|
    DE4038471A1|1990-12-03|1992-06-04|Degussa|METHOD FOR DOPING AQUEOUS SOLUTIONS WITH ACROLEIN IN A BIOCIDALLY EFFECTIVE CONCENTRATION|
    US5925794A|1993-06-08|1999-07-20|Novus International, Inc.|Process for the preparation of 3-propanal|
    US5637766A|1993-06-08|1997-06-10|Novus International, Inc.|Process for the preparation of 3- propanal|
    US5352837A|1993-06-08|1994-10-04|Novus International, Inc.|Process for the preparation of 3-propanal|
    US5663409A|1995-06-07|1997-09-02|Novus International, Inc.|Process for the preparation of 3- propanal and 2-hydroxy-4- butanenitrile|
    US5905171A|1995-06-22|1999-05-18|Novus International, Inc.|Process for the preparation of 3-propanal|
    US5825369A|1996-01-16|1998-10-20|International Business Machines Corporation|Compression of simple geometric models using spanning trees|
    EP0891316B1|1996-04-01|2003-05-21|Union Carbide Chemicals & Plastics Technology Corporation|Processes for the manufacture of methylmercaptopropanal|
    FR2835831B1|2002-02-12|2006-09-01|Aventis Animal Nutrition Sa|PROCESS FOR PURIFYING ACROLEIN|
    DE102004038053A1|2004-08-05|2006-04-27|Degussa Ag|Process for the preparation of 3-propanal|
    DE102010064250A1|2010-12-28|2012-06-28|Evonik Degussa Gmbh|Process for the preparation of methylmercaptopropionaldehyde|
    CN104045590B|2012-04-28|2016-06-29|宁夏紫光天化蛋氨酸有限责任公司|The thick methyl mercapto of methanthiol and acrylic aldehyde synthesis is for the process system of propionic aldehyde|
    EP2679579A1|2012-06-27|2014-01-01|Evonik Industries AG|Integrated method for producing acrolein and 3-Methylmercapto propionaldehyde|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR7917827A|FR2460925B1|1979-07-10|1979-07-10|
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