• 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:
    A process for producing dimethyl ether (DME) from CO and H2, and possibly also CO2, is disclosed in which the gaseous reactants are reacted in the presence of a catalytic composition constituted overall by a mixture of: (a) crystalline silica in which some silicon atoms in the crystal lattice have been replaced by aluminium, and which corresponds to the general formula: Si1Al (0.0012 &cirf& 0.0052)Oy where y varies between 2.0018 and 2.0075; and (b) a mixture of Cu/Zn/Cr and/or Cu/Zn/Al oxides and/or salts; the Al can also be present together with the Cr. Good yields of DME can be achieved at temperatures lower than those normally associated with the dehydration of methyl alcohol to produce DME.
    公开号:SU1329614A3
    申请号:SU823449249
    申请日:1982-06-01
    公开日:1987-08-07
    发明作者:Манара Джованни
    申请人:Снампрогетти С.П.А. (Фирма)；
    IPC主号:
    专利说明:

     one
    The invention relates to an improved process for the preparation of dimethyl ether, which finds use as a solvent, as well as an intermediate in the preparation of polymers, herbicides and other products of organic synthesis,
    The purpose of the invention is to simplify the process.
    Example 1; 1076 g of Cu (N03), 327 g of ZnlNOj} TjHO and 37 g of sodium aluminate are dissolved in water. The solution is heated to 8 ° C and a 10% solution of NaOH in water is added with stirring until the pH is 7.5.
    The solution is cooled, the precipitated precipitate is separated from the liquid by decantation. The precipitate is washed several times with water. In this case, the liquid separation is carried out by decantation, and the last time - by filtration.
    The precipitate is dried in a stream of air in the oven at. The dried material is ground to obtain ASTM 20 mesh particles (0.84 mm). The ground material is mixed with 325 g of silicon oxide modified with γ-alumina. The resulting powder is pressed into tablets with a diameter of A mm and a thickness of 6 mm.
    The catalyst thus prepared contains metals with an atomic ratio of Cu: Zn: Al; Si 28: 11: 7: 54.
    100 g of this catalyst is placed in a tubular reactor with a diameter of 2.54 cm, in the middle of which is placed axially a thermocouple in a shell with a diameter of 8 mm. A mixture of H and N is fed into the reactor and the temperature is gradually increased to 230 ° C. When this occurs, the restoration of the catalyst. When the temperature reaches 230 ° C, the reduction of the catalyst is stopped.
    A pressure of 7000 kPa and a mixture of H and N are gradually replaced in the reactor with a mixture of CO and H (molar ratio 1: 1) and the process is carried out at a mixture flow rate of 2100 h. The resulting reaction mass containing water, methanol and dimethyl ether ( DU) are sent to a cooler located at the outlet of the reactor. In the refrigerator, condensation of water, methanol and part
    dme
    Gas from the reactor is withdrawn through the sampling valve and analyzed by the I1KX method, then the gas is directed to the flow meter.
    At a conversion of 69%, selectivity of the conversion of CO to DME is reached: 63.4%, selectivity for methanol, 3.0%, for carbon dioxide, 33.6%. Other products formed in less than 1% are not considered.
    Example 2. The preparation of the catalyst and the carrying out of the process are carried out analogously to example I. The atomic ratio of Cu: Zn: AI: Sie 28: 11: 7: 54. The feed rate of the raw material is 250С..Ч, the molar ratio Hj:: CO 2: 1. With a conversion of 60%, a selectivity of conversion of CO to DME of 63.0% is achieved; methanol selectivity of 4.2%; carbon dioxide 32.8%
    Example 3. The preparation of the catalyst and the carrying out of the process are carried out analogously to example 2, the process temperature is 240 ° C, the pressure is 9000 kPa, the molar ratio H:: CO 3: 1.
    With a conversion of 61%, the selectivity of conversion of CO to DME is 62.8%; methanol selectivity of 3.5%; carbon dioxide 33.7%.
    Example 4. The preparation of the catalyst and the carrying out of the process are carried out analogously to example 2, the feed rate is 2000 hours, the molar ratio H: CO is 1: 1. Synthesis gas containing 47% Hj is used as the raw material; WITH 47%,
    CO ,. 61. l
    With a conversion of 58%, the selectivity of conversion of CO to DME is 62.5%; methanol selectivity of 3.4%; carbon dioxide selectivity of 34.1%.
    Example 5 Preparation of the catalyst and carrying out the process are carried out analogously to example I. The atomic ratio of Cu: Zn: Al: Sf 30:15:: 10: 45. Pressure 8000 kPa.
    With a conversion of 67%, a selectivity of CO conversion to DU of 62.6% is achieved; methanol selectivity 4.4% carbon dioxide selectivity 33
    Example 6. The preparation of the catalyst and the carrying out of the process are carried out analogously to example 5, The atomic ratio of CU: Zn: A1: Si: Cr 25.9: 14: 0.1: 50: 10. The feed rate of raw materials 2000, pressure 11000 kPa,
    - 1329614
    With a conversion of 59%, a selectivity of conversion of CO to DME of 63.6% is achieved; methanol selectivity of 3.5% carbon dioxide selectivity of 32.9%.
    Thus, the proposed method allows to carry out the process at a conversion of 58 - 69% with selectivity, conversion of CO into DME 61.8 - 64.1% and a temperature of 220 - 240 ° C, whereas in the known method at a conversion of 56 - 62% and selectivity of conversion of CO to DME 60.8 - 63.2%; the process is carried out at 260 -. At the same time, in the proposed method, the catalyst stably operates for a long time - no less than 810 hours. The conversion of CO during this period decreases from 64 to 60.5%, whereas in the known method already after 264 hours the conversion of CO decreases from 62 to 57%.
    权利要求:
    Claims (1)
    [1]
    Claims 50
    The method of producing dimethyl ether by the interaction of hydrogen and carbon monoxide, taken at a molar ratio of 1-3: 1, with
    VNIIPI Order 3499/58 Circulation 371
    Random polygons pr-tie, Uzhgorod, st. Project, 4
    Example 7. Under the conditions of Example 1, the process was conducted for 810 hours.
    The results of obtaining DME from CO and
    HI presented in the table.
    elevated temperature and pressure of 7000-11000 kPa in the presence of a catalyst comprising oxides of silicon, aluminum, copper and zinc, characterized in that, in order to simplify the process, a catalyst of the formula
    Si AlbCUcZn O,, or formula
    Sic, AlbCUcZn Cr, 0.,
    where x is the amount of oxygen satisfying all valences: a 45-54; 0.1-10;
    b c d f
    25.9-30;
    11-15;
    ten,
    and the process is carried out at a temperature of 220-240 ° C and a bulk feed rate of 2000 to 2500 hours.
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    类似技术:
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    同族专利:
    公开号 | 公开日
    IT1137176B|1986-09-03|
    AU553865B2|1986-07-31|
    BR8202979A|1983-05-03|
    DE3220547C2|1983-07-07|
    MX158200A|1989-01-16|
    YU111382A|1985-04-30|
    ES8305297A1|1983-04-01|
    ES513916A0|1983-04-01|
    AU8441482A|1982-12-09|
    GR76005B|1984-08-03|
    FR2506756A1|1982-12-03|
    AR230829A1|1984-07-31|
    LU84166A1|1983-04-13|
    IN155752B|1985-03-02|
    PH17161A|1984-06-13|
    CH649519A5|1985-05-31|
    NO155488C|1987-04-08|
    FI821958L|1982-12-03|
    GB2099327B|1984-09-19|
    NL8202206A|1983-01-03|
    ZA823801B|1983-04-27|
    DE3220547A1|1983-01-20|
    CU21425A3|1987-01-13|
    SE8203409L|1982-12-03|
    DK239982A|1982-12-03|
    NO155488B|1986-12-29|
    FI821958A0|1982-06-02|
    GB2099327A|1982-12-08|
    JPS57204229A|1982-12-14|
    BE893373A|1982-12-01|
    NO821816L|1982-12-03|
    NZ200599A|1985-04-30|
    DD208973A5|1984-04-18|
    PL236730A1|1983-01-31|
    CA1182797A|1985-02-19|
    KR830010034A|1983-12-24|
    IT8122081D0|1981-06-02|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US1177167A|1914-06-30|1916-03-28|Levis Miller Booth|Apparatus for purifying liquids.|
    IT972655B|1972-12-20|1974-05-31|Snam Progetti|PROCEDURE FOR THE PRODUCTION OF DIMETHYL ETHER|
    DK155176C|1978-06-22|1989-07-17|Snam Progetti|PROCEDURE FOR THE PREPARATION OF ALUMINUM OXIDE MODIFIED SILICON Dioxide|
    US4341069A|1980-04-02|1982-07-27|Mobil Oil Corporation|Method for generating power upon demand|US4590176A|1984-06-05|1986-05-20|Shell Oil Company|Catalyst for dimethyl ether synthesis and a process for its preparation|
    IT1207499B|1985-07-26|1989-05-25|Montedipe Spa|PROCEDURE FOR THE OXIDATION OF FLUORINATED OLEFINS AND CATALYST SUITABLE FOR THE PURPOSE.|
    AU602438B2|1988-01-14|1990-10-11|Air Products And Chemicals Inc.|One-step process for dimethyl ether synthesis utilizing a liquid phase reactor system|
    DE3876790D1|1988-05-04|1993-01-28|Rwe Dea Ag|IMPROVED METHOD FOR PRODUCING PURE DIMETHYL ETHER.|
    CA2020929A1|1989-07-18|1991-01-19|Thomas H. L. Hsiung|One-step liquid phase process for dimethyl ether synthesis|
    WO1993010069A1|1991-11-11|1993-05-27|Nkk Corporation|Process for producing dimethyl ether|
    US5344365A|1993-09-14|1994-09-06|Sematech, Inc.|Integrated building and conveying structure for manufacturing under ultraclean conditions|
    DK173614B1|1999-02-02|2001-04-30|Topsoe Haldor As|Process for preparing methanol / dimethyl ether mixture from synthesis gas|
    KR100812099B1|2006-11-28|2008-03-12|한국가스공사|Method of preparing catalyst for making dimethylether from syngas with carbon dioxide|
    FR2909666B1|2006-12-08|2009-03-06|Centre Nat Rech Scient|DEHYDRATION OF METHANOL TO DIMETHYL ETHER EMPLOYING CATALYSTS BASED ON ZEOLITHE SUPPORTED ON SILICON CARBIDE|
    EP2072491A1|2007-12-17|2009-06-24|BP p.l.c.|Process for the conversion of alcohol into alcohol with increased carbon-chain|
    EP2072486A1|2007-12-17|2009-06-24|BP p.l.c.|Process for the conversion of hydrocarbons to ethanol|
    EP2072492A1|2007-12-17|2009-06-24|BP p.l.c.|Process for the conversion of hydrocarbons to ethanol|
    EP2357037A1|2010-02-17|2011-08-17|LANXESS Deutschland GmbH|Method for producing mechanically stable shaped catalysts|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    IT22081/81A|IT1137176B|1981-06-02|1981-06-02|PROCESS FOR THE PRODUCTION OF DIMETHYLETER|
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