• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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  • 引用文献
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    • 专利摘要:
    1531798 Hydrocarbon chlorination catalyst STAUFFER CHEMICAL CO 7 Oct 1976 [5 Nov 1975] 41704/76 Heading B1E [Also in Division C2] In a process for chlorinating ethylene a fixed catalyst bed comprises a mixture, i.e. alternate layers or a random mixture, of metallic iron and particles of activated alumina impregnated with feric chloride either by prior treatment or by in situ deposition by the action of chlorine on the metallic iron, in which the ratio of the superficial surface area of the iron to the total BET surface area of the alumina particles ranges from 1.5 times the total surface area of the inner reactor wall divided by the total BET surface area of the alumina, or 1 x 10<SP>-7</SP>, whichever is greater, to 2 x 10<SP>-6</SP>.
    公开号:SU795450A3
    申请号:SU762416998
    申请日:1976-11-03
    公开日:1981-01-07
    发明作者:Джеймс Зайгенхаген Эллин；Гордон Кэмпбелл Рамсей
    申请人:Стауффер Кемикал Компани (Фирма)；
    IPC主号:
    专利说明:

    one
    Invented: e relates to a method for purifying the gases of the chlorination and oxychlorination of ethylene.
    In many ethylene chlorination or oxychlorination processes, the conversion of ethylene is not completely complete. The effluent from the chlorinating or oxychlorinating reactor contains, in addition to the reaction products, from 0.1-15% by weight and sometimes up to 20% by weight: unreacted ethylene as well as hydrochloric acid, oxygen, inert gases, etc. Modern, aimed at protecting the environment tendencies of the maximum possible decrease in the content of hydrocarbons in the atmosphere, the high cost of ethylene, determines the real need to extract unreacted ethylene, as well as other low aliphatic chlorohydrocarbons.
    A known method of purification of gases of the process of chlorination or oxychlorination of ethylene from ethylene and other lower aliphatic chlorohydrocarbons by treatment with chlorine at a temperature of 80-250s in the presence of a catalyst - iron or iron deposited on HHepTHRft carrier 1. The degree of conversion of chlorine is 99.5%.
    The aim of the invention is to improve the quality of the exhaust gas product after the purification step and reduce the pollution of the environment.
    The quality of cleaning in a known way is low, and the release of such gases into the surrounding environment significantly pollutes the atmosphere.
    The goal is achieved
    the described method of purification of gases of the chlorination process or oxychlorination of ethylene from ethylene and other lower aliphatic chlorohydrocarbons by treatment with chlorine at 100,250 0, preferably at lOO-lSO c and pressure 2-6 atm in the presence of a catalyst - a mixture of 15-20 wt.% iron and 80- 85 wt.% Activated alumina impregnated with ferric chloride, in the amount of 1-5 weight.% In the calculation of alumina. Preferably, the process is carried out at a contact time of 2-30 s, with a volumetric feed rate of the original gases of 50-2QOO h.
    In practical implementation, the method is applicable for cleaning off gases containing up to 7-10 vol.% Of ethylene. After the purification, the ethylene content is less than 50 vol / ppm.
    and chlorine levels below 200 ppm by volume.
    The method of the present invention can reduce the ethylene content to about 1 ppm, and chlorine to about 5 ppm, by adjusting the temperature and the holding time.
    FIG. Figure 1 shows a flow chart for the removal of chlorine from a chlorine-rich waste stream and partially chlorinated saturated hydrocarbons; Fig. 2 is the same in combination with the flax removal system.
    Pipeline 1 (Fig. 1) is fed with chlorine-rich gas flow to heat exchanger 2, which raises the temperature of the stream to about 90-250 ° C, preferably to about 100ISO C, and enters reactor 3, which is a fixed-bed reactor. In the catalyst used, the ratio of the iron surface to the total surface of the BET alumina varies from about 1.5 times the surface area of the inner wall of the reactor divided by the total surface area of the BET alumina containing here.
    The new catalytic mixture is particularly effective when used in non-corrosive vessels.
    The term catalytic mixture is understood to mean a zonal structure in which metallic iron layers are alternated with layers of impregnated catalyst and a quasi-homogeneous state when one of the components of the mixture is randomly or almost evenly dispersed in the other component. Metallic iron is present in the form of accessories in a prod- uct of iron packing, scrap iron or in any other form in which iron is present in metallic form.
    The reactor 3 can be made in the form of a reservoir or made tubular. It can be designed for an upward or downward flow of gaseous reactants. The reactor 3 operates at a temperature of 90-250 ° C, preferably 100-180 ° C. The pressure is about 1-5 atm. The wastewater from the reactor 3 contains chlorination of hydrocarbons that have generally undergone more intensive chlorination than the hydrocarbons in pipeline 1; small amounts of unreacted ethylene and chlorine; the unreacted components of the previous operation and the passage of inert gases through the system. This effluent flows through conduit 4 to separation zone 5, where ethylene chloride and heavier chlorinated impurities are separated. The mass of outgoing gases, consisting mainly of inert gases and small amounts of hydrogen chloride, is discharged through line 6. After removal of the hydrogen chloride by means of proper technical means, the outgoing gas contains only permissible amounts of ethylene and chlorine and is released into the atmosphere. Depending on the reaction temperature and the back-up time, the ethylene content is less than 50 ppm, often even less than 1 vol.h / mln. The chlorine content is less than 200 ppm, often even less than 50 parts by volume / mlM. From the separation zone through the pipeline 7, the liquid phase enters for further purification.
    FIG. Figure 2 shows the method of this invention, which is an improvement of the method for extracting ethylene from an ethylene-containing stream, ilo pipeline 8 is supplied with a mixture of ethylene and other components, from which ethylene is removed by reaction with chlorine to produce ethylene chloride. Pipeline 8 may serve as an outlet from the ethylene chlorination or oxychlorination system. In this case, the mixture contains chlorinated hydrocarbons (saturated and unsaturated) and, possibly, inert gases, for example nitrogen, which passed, without entering into reaction, through a chlorination or oxychlorination system. Chlorine is fed through line 9, with approximately a 0.310% molar excess of ethylene contained in line 8. Chlorine is contacted with an ethylene-containing mixture in a tubular reactor 10 with an exothermic reaction over a catalyst that consists of activated alumina particles with a uniform specific surface or with a mixed specific surface, either in a mixture or in the form of layers with an approximately constant surface area. The reactor 10 is designed to work with the upstream or
    gas flow. The inlet temperature ranges from about 50 to 200 ° C. The maximum temperature of the reactor is approximately 100-250 0. The pressure ranges from about 1 to 5 atm. The waste stream from reactor 10 contains ethylene chloride, small amounts of unreacted ethylene, unreacted chlorine, all other impurities, inert substances, and unreacted components contained in the feed streams or formed as a result of side reactions occurring in the reactor 10, such as oxidation reactions or chlorine reactions. with compounds other than ethylene.
    Alternatively, as shown in FIG. 2 technological schemes, it is possible to introduce the reactor 3 into the reactor
    10. The catalyst bed of the reactor 3 in this case becomes an additional zone located after the reactor 10.
    The term activated alumina according to the invention is any porous absorbent form of alumina obtained by the Bayer method or an equivalent method from an unclean compound, such as bauxite, heated to a controlled temperature that is sufficiently high to distill all bound water, but low enough for. maintaining all required surface area.
    In the following: Examples 1X all experimental data were obtained in the diagram of FIG. 2, Reactor 10 consists of a nickel pipe 3660 mm long and 51 mm in diameter, surrounded by the entire length of 102 mm by a stringer. Heat of reaction is removed by boiling water, the temperature of which in the annular space between the two pipes is maintained at a pressure of 1 at. The temperature of the overheating site and its position along the side of the Katschizagor layer are measured using a mobile thermocouple spreading inside a 6.35 mm diameter thermowell located at the bottom of the reactor - along its entire length.
    The catalyst bed in reactor 10 is divided into three zones, each 762 mm long. In the upper zone, alumina mark A 3235 with a diameter of spherical particles of 6.35 mm is used as a catalyst. Alumina has the following characteristics: Abrasion hardness,% 90 (minimal) Losses during ignition (),
    weight,% . 3 (maximum Sieve Analysis, weight,% (according to Tayle RU)
    +2.5 mesh 0.5 (maximum)
    -2.5 + 3.5 mesh 90 (minimum). -3.5 + 4 mesh 10 (maximum)
    -4 mesh 1.0 (maximum).
    The filled average z.onu k; atalizator (6.35 mm spherical shape) has the following characteristic:
    Volume weight.kg / m, 640t48 Specific surface area (WET), m / g Abrasion hardness, weight,% 90 (minimum Loss on ignition (ZOOOS). Wt.% 5 (Maximum)
    The lower zone is filled with a catalyst that has a spherical shape of particles and the following characteristic:
    Specific area of around 250 + 25 surface (BET), m / g Bulk density, kg / m 640 + 48. Losses when prokalivy5 (maxiniooOO C), wt.% Minal)
    Hardness at abrasion 90% (min%,%)
    Specific pore volume, cm g0.44
    The average pore diameter (BET), A64-70
    five
    A pore volume of 80-600 A is 2037% of the total pore volume.
    Reactor 3 consists of 6.1 m steel pipe with a diameter of 102 mm. The highest 3620 mm pipes are lined from inside with nickel. The catalyst bed is about 2290 mm in each of the examples described below and is located at the top of the reactor. The temperature of the catalyst is measured by a mobile thermocouple placed in
    S thermowell, a reactor inserted upwards and a tubing along its entire length.
    The feed through conduit 8 in each case contains 7 mol.% Of ethylene, 1 mol% of oxygen, 4 mol.%
    0 ethylene chloride, 1 wt.% Water, the rest is nitrogen. The pressure at the inlet to the reactor 10 is maintained at 3.5 atm. The feed rate of gases 50.6 cm / s.
    To calculate the chlorine concentration and
    5 Hydrochloric acid, a waste stream in line 4 is bubbled through a solution of potassium iodide and collected in a vessel to displace water having a known volume. In addition, part
    0 of the output stream is condensed and the liquid and gas phases are analyzed (after condensation) by nyTet-i gas chromatography. The results are compiled (together with the results of the titration) into the overall material balance, on the basis of which the percentage of excess chlorine and other data presented in the tables are calculated. Example. The catalyst layer consists of Pala rings 16mm thick,
    0 packed with a thickness of about 70 mm, intermittently with layers of a thickness of 310 mm of alumina catalyst impregnated with ferric iron, and the iron content is
    5 to 2 wt.%; Pal rings are about 18 vol.% Of the catalyst bed. Data characterizing the flow of exhaust gases after 220 and 250 hours of operation are summarized in table 1.
    The results obtained with a small
    The residence time in the reactor is given in table 2.
    Table
    权利要求:
    Claims (4)
    [1]
    Claim 1. The method of purification of gases of the process of chlorination or oxychlorination of ethylene by treatment with chlorine at a temperature of 100-250s in the presence of an iron-containing catalyst, which is used as an iron catalyst to improve the quality of the target product and reduce environmental pollution. a mixture of 1520 wt.% iron and 80-85 wt.% activated alumina impregnated with ferric iron in an amount of 1-5 wt.% based on alumina, and the process is carried out at a pressure of 2-6 atm.
    table 2
    [2]
    2. Method POP1, characterized in that the process is carried out at a temperature of lOO-lSOOc.
    [3]
    3. Method POP1, characterized in that the process is carried out at the time of contact with ..
    [4]
    4. A method according to claim 1, characterized in that the process is carried out at a volumetric feed rate of source gas from 50-2000. Sources of information taken into account in the examination 1. French patent 1.421903, cl. From 0.7 s, publish .. 22,01.65 (prototype).
    - & iL
    FIG. I
    iff.2
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    同族专利:
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    EG12642A|1979-09-30|
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    IL50840D0|1977-01-31|
    FR2330438B1|1980-04-04|
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    PT65796B|1978-05-12|
    NO763756L|1977-05-06|
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    IL50840A|1978-09-29|
    AT346293B|1978-11-10|
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    IN144967B|1978-08-05|
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    引用文献:
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    US2160574A|1937-05-10|1939-05-30|Ig Farbenindustrie Ag|Manufacture of carbon tetrachloride|
    US2246082A|1939-08-22|1941-06-17|Shell Dev|Preparation of alkyl halides|
    US2393367A|1943-05-14|1946-01-22|Us Ind Chemicals Inc|Manufacture of dichlorethane|
    US2658088A|1949-01-25|1953-11-03|Chempatents Inc|Chlorination of ethylene in dilute mixtures|
    GB1186557A|1966-07-22|1970-04-02|Solvay|Improvements in or relating to the manufacture of Chlorinated Hydrocarbons|
    FR1598840A|1968-12-27|1970-07-06|JPS6241488B2|1979-10-31|1987-09-03|Kanegafuchi Chemical Ind|
    FR2493307B1|1980-11-04|1984-08-10|Ugine Kuhlmann|
    DE3331962A1|1983-09-05|1985-03-21|Wacker-Chemie GmbH, 8000 München|METHOD FOR TREATING CHLORINE HYDROGEN AS A SUBSTANCE FOR THE ETHYLENE OXICHLORATION PROCESS|
    US4590317A|1984-08-06|1986-05-20|The B. F. Goodrich Company|Process for minimizing corrosion and coking in an ethylene dichloride plant|
    JPS61180730A|1985-02-06|1986-08-13|Mitsubishi Chem Ind Ltd|Method for purifying 1,2-dichloroethane|
    DE102013216823A1|2013-08-23|2015-02-26|Siemens Aktiengesellschaft|Storage device for stackable containers|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US05/629,171|US4029714A|1975-11-05|1975-11-05|Ethylene/chlorine elimination process|
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