• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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  • 优先权
    • 专利摘要:
    1475309 Maleic anhydride UCB 1 Aug 1974 [3 Aug 1973] 36943/73 Heading C2C [Also in Division B1] Maleic anhydride is made by the vapour phase oxidation of butane in the presence of an oxidic catalyst comprising phosphorus, vanadium and cobalt and/or nickel. The catalyst may be in a fixed or fluidized bed and have 0À5 to 3 atoms of phosphorus and 0À05 to 0À5 atoms of Group VIII metal per atom of vanadium. The reaction conditions may be 1-4% v butane, 99-96% v air, 350-550‹ C., at least atmospheric pressure and a contact time of 0À5-45.
    公开号:SU961556A3
    申请号:SU742051858
    申请日:1974-08-02
    公开日:1982-09-23
    发明作者:Лемал Рене；Векеманс Жак
    申请人:Юцб С.П.А. (Фирма)；
    IPC主号:
    专利说明:

    This invention relates to a method for producing maleic anhydride. A known method for producing maleic anhydride by oxidizing butane on a P / V / Fe catcher is 13. However, the yield of the target product is low and does not reach 30 wt.%. The closest to the present invention is a method for producing maleic anhydride by oxidizing butane with molecular oxygen in the vapor phase at 300-650 ° C in the presence of a katashizor containing phosphorus and vanadium in an oxidized form and additionally containing as an activator of zin copper Thereby, the P / V / activator ratio is 0.5–5 / 1 / 0.05–0.5. The yield of the target product is 94% at 12. However, the known method has an insufficiently high yield of the target product. Lel invention - an increase in the yield of the target product. This goal is achieved by the method of producing maleic anhydride by catalytic oxidation of butane with molecular oxygen in the vapor phase at 330-480 ° C in the presence of a catalyst containing phosphorus and vanadium in the oxidized form, additionally containing cobalt with a ratio of constituents in the catalyst equal to 1 10-1.14: 1: 0.10-0.25. Example 1. Production in the aquatic environment of the catalyst P / V / O, used as a control sample, and obtaining the proposed proposed catalysts. Dissolve with reverse flow of 65.1 parts by weight. pentooxidine 1000 tbsp concentrated hydrochloric :: lots. After 4 hours of heating, the activator is added during the reverse flow, boiling is maintained for 2 hours during the reverse flow, then phosphoric acid is added. Boiling at the reverse flow is maintained additionally for 6 hours, and then the solution is evaporated to dryness. The solid residue is dried at 120 ° C for 12 hours, coarse crushed, and then heated at 350 ° C for 4 hours. After cooling, the residue is ground and screened on a sieve containing 36 cells per cm. To the powder is added graphite in sufficient quantity so that the mixture contains
    its 1 wt.%, and compressed into tablets of 5 mm. Tablets were crushed, and the part passing through a sieve with a 1.6 mm hole and not passing through a sieve with 1 mm holes was used to load the reactor.
    In tab. 1 shows the amount and nature of the activator used and the added amount of phosphoric acid for 65.1 h by weight of vanadium pentoxide.
    Example 2. Preparation in the alcohol environment of the catalyst .P / V / 0, used as a control sample, and activated the proposed catalysts.
    In 1000 parts by weight, the solvent is added to the suspension 227.35 parts by weight. vanadium pentoxide and the desired amount of activating metal.
    Through the immersed tube, 330 parts by weight hydrochloric acid in dry gaseous form is added at such a rate that the temperature does not exceed 40 ° C. Vanadium pentoxide dissolves.
    On the other hand, at 250 weight.h. the solvent dissolves the required amount of phosphoric acid. The first solution is added to the second one and the mixture thus obtained is heated for 90 minutes during the reverse flow, the solvent is evaporated and the solid residue is dried at 150 ° C for 6 hours.
    After cooling, the residue is milled, sieved and turned into tablets as described in Example 1. The tablets are milled, and a portion of 1-1.5 mm in size serves to load the reactor.
    And table. 2 shows the amount of activator used, the nature of the solvent and the amount of phosphoric acid used for 227, 35 parts by weight. vanadium thioxide.
    In the following examples, the yield obtained using the proposed catalyst is given.
     The catalyst is placed in a glass microreactor with an inner diameter of 8 mm, equipped with a thermometric jacket with an outer diameter of 4 mm. The catalyst volume is equal to 4.15 mp. The residence time is equal to the ratio of catalyst to the flow rate of air-butane mixing, calculated in ml / s under normal conditions of temperature and pressure (and 760 mm Hg). Vvkod maleic anhydride. Equal to the ratio multiplied by 100, the weight of the anhydride obtained to the weight of the introduced butane.
    Example 3. The yield obtained using the proposed activators is, on average, equal to or greater than the highest yield obtained by the known method C2J, which is 94% by weight for a temperature of 476 ° C and with a contact time of 4.09 s (if you express the results known method under normal conditions of temperature and pressure). The results are shown in Table. 3
    Example 4. The addition of the proposed activators makes it possible to circumvent the heat treatment required for V / P catalysts.
    The results are shown in Table. four.
    Thermal treatment (A) consists in heating the catalyst in air at a spatial velocity of 120 v / v / h. before, and then in maintaining this temperature for 1 h.
    The temperature is then adjusted to 414 ° C in an air-butane atmosphere (1.5% volume) at a speed of 120 rpm. gas / / about, catalyst / h.
    The spatial rate is then adjusted to 700 v / v / h, while the catalyst is heated to about 470 ° C at a rate of about 5-10 ° C per hour.
    Thermal treatment (B) consists in heating the catalyst at a rate of a minute (in air flow at a speed of 1.5 v / v / m. This temperature is maintained for 2 hours.
    Tegperature is then adjusted from 380 to 480 ° C at a rate of 3 ° C per minute, while air-butane stream containing 1.5% by volume of butane is passed at the flow rate. 1.5 rev / rev / min The temperature at 480 ° C and the flow rate of the air-butane mixture are maintained for 16 hours. The temperature is then lowered to 420 ° C, while the flow rate of the mixture is increased to 17 vol / v / min. The temperature is controlled in such a way that the conversion of butane is 90%.
    The catalysts that are not subjected to heat treatment start from an ambient temperature, the flow rate of an air-butane mixture (1.5% by volume), calculated in such a way as to achieve the required residence time, and the temperature rises with the maximum speed, which ensures heating of the microreactor.
    Table 1
    Ievesnny katgshieator
    450 450 480. 453 431 405 387 410 405 432 330
    Table 3
    权利要求:
    Claims (2)
    [1]
    1. For Germany FRG 2248746,, cl. 12 About 21, pub. 1972.
    [2]
    2. The patent of Belgium 791294, cl. C 07 C, publ. 1972.
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    同族专利:
    公开号 | 公开日
    FR2245651B1|1978-07-07|
    BE818360A|1975-02-03|
    TR18209A|1976-11-25|
    FI228374A|1975-02-04|
    PL100068B1|1978-08-31|
    AR201783A1|1975-04-15|
    ATA634874A|1976-06-15|
    JPS5069016A|1975-06-09|
    CH585169A5|1977-02-28|
    AT334870B|1977-02-10|
    DE2437154C2|1983-11-17|
    FR2245651A1|1975-04-25|
    IN140361B|1976-10-23|
    ZA744950B|1975-08-27|
    BR7406326D0|1975-05-20|
    DE2437154A1|1975-02-13|
    JPS5745233B2|1982-09-27|
    DD113215A5|1975-05-20|
    RO66350A|1979-07-15|
    BG32563A3|1982-08-16|
    AU7188374A|1976-02-05|
    NL7410242A|1975-02-05|
    GB1475309A|1977-06-01|
    ES428793A1|1977-01-01|
    CS190433B2|1979-05-31|
    IT1018793B|1977-10-20|
    FI63395C|1983-06-10|
    CA1036168A|1978-08-08|
    US3987063A|1976-10-19|
    HU168988B|1976-08-28|
    EG11525A|1977-08-15|
    SE7409810L|1975-02-04|
    FI63395B|1983-02-28|
    SE419547B|1981-08-10|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    RU2607762C2|2011-05-11|2017-01-10|ХАНТСМЭН ПЕТРОКЕМИКАЛ ЭлЭлСи|Improved solvent for extraction of maleic anhydride from gas stream|DE1146844B|1960-12-14|1963-04-11|Thyssensche Gas Und Wasserwerk|Process for coking gas-rich coals for the production of ore coke|
    US3856824A|1971-12-27|1974-12-24|Monsanto Co|Modified p-v-fe catalyst for production of maleic anhydride from saturated aliphatic hydrocarbons|
    BE791294A|1972-01-03|1973-05-14|Chem Systems|BUTANE OXIDATION PROCESS TO FORM MALEIC ANHYDRIDE|
    US3888886A|1972-06-08|1975-06-10|Mobil Oil Corp|Oxidation of alkanes to maleic anhydride using promoted vanadium-phosphorus catalyst|US4064070A|1974-12-23|1977-12-20|Chevron Research Company|Catalyst for producing maleic anhydride|
    US4018709A|1975-03-17|1977-04-19|Petro-Tex Chemical Corporation|Catalyst for preparing maleic anhydride from C4 hydrocarbons|
    US4056487A|1975-10-02|1977-11-01|Petro-Tex Chemical Corporation|Vanadium phosphorus oxygen oxidation catalysts useful for preparing anhydrides from alkanes|
    US4092269A|1976-10-15|1978-05-30|Monsanto Company|Phosphorus-vanadium-oxygen catalysts having a specific pore volume|
    US4209423A|1977-05-23|1980-06-24|Imperial Chemical Industries Limited|Production of acid anhydrides and catalysts therefor|
    US4151116A|1977-08-05|1979-04-24|Halcon Research And Development Corporation|Preparation of maleic anhydride|
    DE2966785D1|1978-08-01|1984-04-19|Ici Plc|Driverless vehicle carrying directional detectors auto-guided by light signals|
    CA1148527A|1979-08-27|1983-06-21|Ramon A. Mount|Phosphorus-vanadium-oxygen catalystprecursors and catalysts|
    US4293498A|1980-10-22|1981-10-06|Standard Oil Co.|Preparation of maleic anhydride|
    US4315864A|1980-10-22|1982-02-16|Standard Oil Company |Preparation of maleic anhydride|
    US4396536A|1980-10-22|1983-08-02|The Standard Oil Company|Preparation of vanadium phosphorous catalysts using olefinic oxygenated media|
    JPH024525B2|1980-12-25|1990-01-29|Mitsubishi Chem Ind|
    US4456764A|1982-09-20|1984-06-26|Monsanto Company|Process for the manufacture of maleic anhydride|
    DE3624439A1|1986-07-19|1988-01-28|Basf Ag|METHOD FOR THE PRODUCTION OF MALEIC ACID ANHYDRIDE BY PARTIAL OXIDATION|
    US5288880A|1992-03-17|1994-02-22|Maruzen Petrochemical Co., Ltd.|Process for the manufacture of maleic anhydride|
    DE19727235A1|1997-06-26|1999-01-07|Consortium Elektrochem Ind|Shell catalyst for maleic anhydride production by gas phase oxidation|
    CN108101873A|2016-11-24|2018-06-01|中国石油化工股份有限公司|A kind of method that n butane oxidation prepares cis-butenedioic anhydride|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB3694373A|GB1475309A|1973-08-03|1973-08-03|Process for the production of maleic anhydride|
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