• 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:
    Improved process for the production of sulphur from a gas containing H2S, SO2, H2 and/or CO, in which the gas is caused to pass through a CLAUS catalyst in a primary catalytic stage operating at between 200 DEG and 460 DEG C. in order to form sulphur, and thereafter the sulphur contained in the reaction mixture issuing from this stage is condensed through indirect heat exchange with water to produce steam. The improved process consists in constituting at least the final eighth of the catalyst volume in this stage by a composite mass formed from a refractory oxide on which is fixed a transition metal compound, for example Co and/or Mo, and in entering into contact the gas with this composite mass at between 300 DEG and 460 DEG C. in order to oxidize H2 and CO. The energy resulting from this oxidation is recovered in the form of a supplementary quantity of steam during the sulphur condensation.
    公开号:SU1248531A3
    申请号:SU813358556
    申请日:1981-11-16
    公开日:1986-07-30
    发明作者:Квашникофф Жорж；Вуарэн Робер
    申请人:Сосьете Насьональ,Елф Акитэн (Продюксьон) (Фирма)；
    IPC主号:
    专利说明:

    112
    The invention relates to a method
    receiving and sulfur from gases containing and 50.
    The aim of the invention is to obtain, for an additional amount of water vapor, sulfur production by the Claus method,
    The essence of the method is that the reaction gas mixture after the first stage of contact is passed at 300-400 ° C through a catalyst deposited on a refractory oxide and containing metal compounds selected from the group consisting of molybdenum, vanadium, tungsten, chromium or a mixture thereof a cobalt or nickel compound.
    Moreover, there are two possible ways to carry out the process: in accordance with one variant, the source gas is first passed through a conventional Claus catalyst placed in the first reactor, and then through the proposed catalyst placed in the second reactor.
    Alternatively, the gas first passes through a conventional Claus catalyst, and then through the proposed additional catalytic mass located directly behind the conventional catalyst in the same reactor,
    In both cases, the ratio of the amount of catalyst Claus and the catalytic mass is 1-8: 1, preferably 1-4: 1.
    The contact time of a gas with an additional catalytic mass, depending on the volume of the amount of gas, ranges from 0.5 to 8 s.
    The carrier of the catalytic mass can be chosen from aluminum hydroxides, bauxite, oxides of titanium, zirconium, silica, zeolites, or mixtures of these substances,
    As catalytic active compounds of these metals, their oxides are sulfides, salts of inorganic or organic acids, for example, sulfates, nitrates, phosphates, acetates.
    In addition to HjS and 30, the source gas may also contain H and / or CO within a rather wide range of 0.3-10% by volume.
    HjS-containing gas is subjected to incomplete combustion at 1000-1500 s with a lack of oxygen to produce sulfur and the reaction gas mixture
    j „5

    five
    five
    five
    s with a ratio of H S: SO - 2: 1, the products of combustion are cooled to condense sulfur, and the remaining gas mixture containing T S, SO, H and / or CO is directed to the first catalytic stage, carried out at 200-460 C, Next, the gas is contacted with an additional catalytic mass at 300-400 ° C, with the result that during the conversion of n contained in the gas and CO, additional energy is recovered in the form of water vapor.
    Example 1. The method is carried out in a vertical reactor, simulating the first stage of catalysis, containing a layer of a conventional Claus catalyst over a layer of additional catalytic mass. Conventional catalyst Claus consists of balls of aluminum hydroxide with a diameter of 4-6 mm with a specific surface of 260 m / g. Additional catalytic mass in the form of balls with a diameter of 5 mm and with a specific surface of 248 consists of aluminum hydroxide, impregnated with cobalt oxide and molybdenum oxide i, and contains 1.75 cobalt and 8% molybdenum,
    In the reactor With a flow rate of 1000 nl / h gas is supplied with the following composition, vol.%: H S 9; -SOj 4.5; AND 2; H-, jO 20; N 64.5.
    The gas first passes through a bed of conventional catalyst, then through a bed of additional catalytic mass. Their volumes are selected in such a way that the contact time of the gas is 4 and 1.5 s, respectively. The first layer operates at 250 s, and the second at 335 ° C,
    The sulfur yield for both catalysts is 70%, and at the exit of the second layer is conversion, H is 60%.
    In a similar experiment using a single catalyst with a contact time between the gas and the catalyst 5.5 with a sulfur yield of 70% 5, but hydrogen conversion does not take place.
    The results of experiments using other catalysts are presented in the table.
    In the proposed method, due to the conversion of Hj and CO in the additional layer of catalyst, additional energy is recovered in an amount up to 22x10 J / h, which corresponds to the vapor release of about 10 t / h, i.e. more than 8% compared with the prototype.
    Specifications
    The nature of the metal, which is impregnated substrate W
    Cr
    The amount of this metal in the mass (wt.%)
    16.6 6.2 5.9
    The weight of the additional catalytic mass relative to the total weight of the catalyst,%
    five
    one
    215
    4, 5
    1.5
    324 250
    Order 4144/60 Circulation 450 Subscription
    VNIIPI USSR State Committee
    for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab ,, d.4 / 5
    . Production and printing company, Uzhgorod, Projecto st., 4.
    12A853 4
    Additional catalytic mass
    Mo + Ni W + CO Cr + Ni V + CO MO
    1.2 + 2.1 l4.2-tl, 9 4.7 + 2.34.5 + 1.89.5
    50
    60
    12.5 30
    25
    4.5
    2.4
    5.25 4.2 4.5
    1.5
    3.6
    0.75 1.8 1.5
    293
    261
    285 275 250
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PRODUCING SULFUR FROM hydrogen sulfide-containing gas according to the Klaus method, including burning the source gas, the subsequent interaction of the obtained sulfur dioxide with sulfur;
    hydrogen in a ratio of 1: 2 to several catalytic stages at .200 - 460 ° С, the formation of sulfur formed by condensation after each stage of contacting and heat recovery of the reaction gases to produce water vapor, characterized in that, in order to obtain an additional amount of water vapor, the reaction the gas mixture after the first stage of contacting is passed at 300 - 400 ° C through a catalyst supported on a refractory mixture and containing 5.9 - 16.6 wt.% metal compounds selected from the group consisting of molybdenum, vanadium, tungsten m, or a mixture of chromium with nickel or cobalt compound.
    SU "" 1248531 AZ
    1 1248531
    类似技术:
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    US3917797A|1975-11-04|Removal of contaminants from gaseous streams
    同族专利:
    公开号 | 公开日
    DE3145642A1|1982-08-12|
    FR2494255B1|1984-12-14|
    IT1144930B|1986-10-29|
    NL8105179A|1982-06-16|
    IT8125125D0|1981-11-17|
    NO158215B|1988-04-25|
    GB2087373B|1985-07-24|
    NO158215C|1988-08-03|
    FR2494255A1|1982-05-21|
    US4436716A|1984-03-13|
    NO813884L|1982-05-18|
    JPS57111208A|1982-07-10|
    GB2087373A|1982-05-26|
    CA1166823A|1984-05-08|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    FR2123778A5|1971-01-29|1972-09-15|Inst Francais Du Petrole|
    FR2369209B1|1976-11-02|1981-06-12|Inst Francais Du Petrole|
    US4138473A|1977-10-31|1979-02-06|Gieck Joseph F|Process for recovering sulfur from sour gas|FR2511663B1|1981-08-19|1985-02-15|Elf Aquitaine|
    US4542114A|1982-08-03|1985-09-17|Air Products And Chemicals, Inc.|Process for the recovery and recycle of effluent gas from the regeneration of particulate matter with oxygen and carbon dioxide|
    DE3529665A1|1985-08-20|1987-02-26|Metallgesellschaft Ag|METHOD FOR REMOVING SULDURATE FROM EXHAUST GASES|
    US5185140A|1985-10-25|1993-02-09|Elf Aquitaine Production|Process for removing sulphur compounds from a residual gas|
    FR2589082B1|1985-10-25|1989-12-01|Elf Aquitaine|PROCESS FOR REMOVAL OF SULFUR COMPOUNDS CONTAINED IN A WASTE GAS, PARTICULARLY FROM A CLAUS SULFUR FACTORY, WITH RECOVERY OF SUCH SULFUR COMPOUNDS|
    FR2589140B1|1985-10-25|1991-02-22|Elf Aquitaine|CATALYTIC PROCESS FOR THE PRODUCTION OF SULFUR FROM AN ACID GAS CONTAINING H2S|
    US5494650A|1989-01-19|1996-02-27|Societe Nationale Elf Aquitaine |Process for improving the sulphur yield of a complex for producing sulphur from a sour gas containing H2 S, the said complex comprising a sulphur plant and then an oxidation and hydrolysis unit followed by a purification unit|
    FR2840295B1|2002-06-03|2005-02-04|Inst Francais Du Petrole|PRODUCT FOR REMOVING SULFUR FROM A LOAD CONTAINING HYDROGEN SULFIDE AND BENZENE, TOLUENE AND / OR XYLENES|
    FR2897066B1|2006-02-06|2012-06-08|Inst Francais Du Petrole|PROCESS FOR EXTRACTING HYDROGEN SULFIDE FROM HYDROCARBON GAS|
    CN103482581B|2012-06-12|2016-04-06|中国石油化工股份有限公司|A kind of method of coproduction sulphur and hydrofining product|
    GB2513962A|2013-03-01|2014-11-12|Frank Cross Ltd|Catalytic treatment|
    WO2020089099A1|2018-10-31|2020-05-07|Haldor Topsøe A/S|Method for production of sulfur|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR8024324A|FR2494255B1|1980-11-17|1980-11-17|
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