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    • 专利摘要:
    A process for improving the activity of tellurium containing metal oxide catalysts useful as catalysts for oxidation, ammoxidation or oxidative dehydrogenation of organic compounds by heating the catalysts together with a tellurium containing solid and an optional molybdenum containing solid to a temperature up to about 900 DEG C. in a gaseous atmosphere. The process can be effectively applied to deteriorated or spent catalysts, the activity of which has been deteriorated due to use for a long period of time. The tellurium containing solid used as an activity improving agent is elemental tellurium and the molybdenum containing solid is selected from the group consisting of (i) a molybdenum compound, (ii) at least one molybdenum compound supported on an inert carrier, and (iii) a molybdenum enriched catalyst prepared by adding a Mo component to a metal oxide catalyst (which may be a fresh catalyst or a deteriorated catalyst). In a particularly preferred embodiment, the process for improving the activity according to the present invention can be carried out by contacting the deteriorated tellurium containing metal oxide catalyst with the elemental tellurium and optional molybdenum-containing solid in a fluidized-bed. More preferably, the contact is carried out during the oxidation, ammoxidation or oxidative dehydrogenation reaction.
    公开号:SU1367844A3
    申请号:SU823440811
    申请日:1982-05-14
    公开日:1988-01-15
    发明作者:Сасаки Ютака；Киемия Ютака；Накамура Тосио
    申请人:Нитто Кемикал Индастри Ко,Лтд (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to methods for activating tellurium-containing metal oxide catalysts used in ammonolysis and oxidative dehydrogenation processes.
    The purpose of the invention is to obtain a catalyst with increased activity and selectivity.
    Example 1. In the reaction of ammonium propylene, a fluidized bed catalyst of the following empirical formula is used.
    Fe, oSb ,,, o
    About 67.8 (Slop
    thirty
    with
    during the reaction, the activity decreases - due to a decrease in the molar ratio of oxygen to α-α-propylene. The yield of acrylonitrile is reduced from 80.3% at the initial stage to 78.6%. 10% of this catalyst is removed and replaced with a previously prepared catalyst rich in tellurium.
    Using the resulting mixture of a tellurium-containing catalyst and a tellurium-containing solid compound, the ammoxidation of propylene is carried out.
    A catalyst in the amount of 1200–1800 g is loaded into a fluidized bed reactor having a fluidized catalyst compartment with an inner diameter of 5 cm and a height of 2 m.
    f
    whose activity is reduced as a result of use for a long time. 15.1 g of powdered metallic tellurium are dissolved in 540 g of 45% nitric acid. The resulting solution is made up to 440 ml with 45% nitric acid. The spent catalyst is added to the resulting solution and mixed thoroughly for 1 hour. The mixture is calcined at 200 ° C for 2 hours and then at 350 ° C for 4 hours. The tellurium content in the resulting rich tellurium catalyst is 2.65 wt. %
    Example 2. A fluidized bed catalyst with the following empirical formula is loaded into a fluidized bed reactor with an internal diameter of 20 cm.
    Re, о8Ь „Sys 5
    ° o, g5 1 ° obz, 3
    and the ammoxidation reaction of propylene is carried out.
    The relative velocity of the gas introduced into the reactor is 18 cm / s, the reaction pressure is 0.5 g / kg.
    The molar ratio in the feed gas 0 (in the form of air) is propylene 2.2; NH, is propylene 1.1. Reaction time. 450 ° C.
    When carrying out the reaction under these conditions for 670 h, the yield of acrylic
    In this reactor, the relative linearity of the 35 nitrile is reduced, and the formation of a double velocity of 15 cm / s introduces a gas of the following composition (molar ratio): Oj (in the form of air) is propylene 2.10; NHj - propylene 1,15.
    The reaction is carried out at atmospheric pressure.
    The contact time is determined by dividing the volume of the loaded catalyst (relative to its bulk density) by the flow rate of the feed gas.
    The yield of acrylonitrile after 3 hours is 80.1%.
    The reaction is carried out for an additional 5 hours, but the yield remains the same.
    Used in this example, the tellurium-rich catalyst was prepared as follows,
    Remove 2 kg of fluidized bed catalyst with the following empirical formula
    carbon monoxide increases.
    2 kg of spent catalyst are removed. To the spent catalyst, powdered metal tellurium was added in an amount of 0.2%. In a fluidized bed reactor with an inner diameter of 5 cm, the resulting mixture is charged and fluidized by introducing gaseous nitrogen :. The temperature is gradually increased and maintained at 300 ° C for 1 hour.
    The catalyst thus treated is used for the reaction of ammoxy50 doping of propylene. Under conditions analogous to example 1, the yield of acrylonitrile with the spent catalyst is 76.3% and with the treated 77.8%. Example 3. Remove 2 kg
    55 spent catalyst according to example 2 and 10 g of powdered tellurium dioxide are added to it. The resulting mixture is filled with an internal fluidized bed reactor.
    Fe, o
    0, Z lO
    On, .L810,),
    35 nitrile is reduced, and the formation of two
    carbon monoxide increases.
    2 kg of spent catalyst are removed. To the spent catalyst, powdered metal tellurium was added in an amount of 0.2%. In a fluidized bed reactor with an inner diameter of 5 cm, the resulting mixture is charged and fluidized by introducing gaseous nitrogen :. The temperature is gradually increased and maintained at 300 ° C for 1 hour.
    The catalyst thus treated is used for the reaction of ammoxy50 doping of propylene. Under conditions analogous to example 1, the yield of acrylonitrile with the spent catalyst is 76.3% and with the treated 77.8%. Example 3. Remove 2 kg
    55 spent catalyst according to example 2 and 10 g of powdered tellurium dioxide are added to it. The resulting mixture is filled with an internal fluidized bed reactor.
    3 .1
    5 cm in diameter, after which a gas mixture of nitrogen and water vapor in a 1: 1 ratio by volume is introduced into the fluidized bed. The temperature of the reactor is gradually increased. The reactor was incubated at 500 ° C for 2 hours. The catalyst prepared in this way was used in the oxidation reaction of propylene in the presence of ammonia as in example 1.
    The yield of acrylonitrile using spent catalyst is 76.3%, its yield on the treated catalyst is 78.1%. Example 4 2 kg of spent catalyst of example 2 is removed, 100 g of powder containing 20% of tellurium dioxide supported on silica is added to it, and oxidative ammonolysis (oxidation in the presence of ammonia) of example 1 is carried out.
    The yield of acrylonitrile using spent catalyst is 76.3%, 2 hours after the start of the reaction, it reaches 77.5%, and after 5 and 8 hours it becomes equal to 78.3 and 78.2%, respectively.
    A powder consisting of a mixture of tellurium dioxide and silicon dioxide used in these examples is obtained by the following method.
    160 g of powdered metallic tellurium are suspended in 1500 g of water. After 10 ml of a 15% aqueous ammonia solution was introduced into the suspension, 400 ml of a 35% hydrogen peroxide solution were added in small portions to dissolve the tellurium. To the resulting solution was added 2.67 kg of silica sol containing 30 wt.% SiOji. After the introduction of 240 g of ammonium nitrate, the mixture was spray dried. After annealing, first at 200 ° C for 2 h, and then at 4 (30 ° C for 2 h, the product is subjected to final annealing at 550 C in
    for 4 hours
    Example 5. The reaction was carried out analogously to example 4, except that the ratio of telur dioxide and silicon dioxide in the mixture was 1: 2.
    The yield of acrylonitrile increased to 77.1 m, 77.8% after 5 and 8 hours respectively.
    678444
    Example 6. Remove 2 kg of spent catalyst according to example 1.
    200 g of a powder containing tellurium oxide and 0.5 wt.% Molybdenum oxide deposited on a mixture of silica and alumina are added to this catalyst, after which the mixture is treated at 400 ° C for 3 hours, entering There is a gas mixture consisting of ammonia and air (with an ammonia content of about 9% by volume). Then, oxidative β-monolysis of propylene is carried out in Example 1. The yield of acrylonitrile is increased to 78.4%.
    Powder containing oxides of tellurium and molybdenum, get the next 20 way.
    64 g of powdered metallic tellurium are suspended in 300 ml of water containing 9 g of ammonium paramolybdate, after which the suspension is heated to 95 s. 170 ml of a 35% hydrogen peroxide solution are added to the suspension in small portions to completely dissolve the tellurium. Then the amount of liquid is adjusted to 580 ml. 30. Clean water is added. A catalyst carrier consisting of alumina and silica in an amount of 920 g is added to the liquid and stirred in a mixer for 1 hour. The mixture is then dried at 130 ° C for
    35
    3 h and annealed for 2 h at 400 Siv for 2 h at 500 ° С.
    . Example 7. 40 Propylene oxidative ammonolysis is carried out using a catalyst of the following empirical formula
    Fe, o Sb yCUjMOo y Wo, 3 Te, 5 Pn, (SiO)
    60
    45
    Since a decrease in the molar ratio of oxygen to propylene during the reaction is permissible, the catalyst undergoes a process test. Output
    50 acrylonitrile is 83.2%, even if the conditions of the reaction are normal.
    To this catalyst is added a catalyst rich in tellurium and
    gg of 0.4 wt.% molybdenum with their ratio equal to 7, and the reaction is carried out according to example 1. The output-Acrylonitrile gradually increases, reaching 85.0%
    . 3 h after the start of the reaction.
    51367844
    Tellurium enriched catalyst
     and molybdenum, obtained in the following way.
    1.5 kg of spent catalyst according to Example 2 is removed, 13.5 g of powdered metallic tellurium is dissolved in small portions in 45% nitric acid, 3.75 g of ammonium paramolybdate is dissolved in 10 ml of pure water. The resulting solution is added to the tellurium nitrate solution. After bringing the amount of liquid to 420 ml by adding pure water, the spent catalyst is added and the mixture is thoroughly mixed in a mixer for 1 hour. After heat treatment at 200 ° C for 5 hours and at .400 ° C for 2 hours, the mixture is annealed at 550 C for 4 h.
    Example 8. The process is conducted using a catalyst similar to example 7.
    Since the molar ratio of oxygen to propylene may decrease during the reaction, the catalyst undergoes development. As a result, the yield of acrylonitrile becomes 82.8% even if the conditions of the reaction lead to a standard.
    To this catalyst, the catalyst of Example 7 enriched with tellurium and molybdenum is added in an amount of 3%, after which the reaction is carried out again.
    The yield of acrylonitrile gradually increases and reaches 84.8% after carrying out the reaction for 5 hours.
    Example 9. To the catalyst of example 7 was added a powder of a mixture of alumina and silica prepared in example 4 in an amount of 2%, after which the oxidative ammonolysis of example 1 was reacted.
    The yield of acrylonitrile increased by 0.6%, however, the formation of carbon dioxide and HCN is slightly reduced.
    In this example, fresh catalyst (not developed), treated according to pre-10, is used.
    15
    20
    25
    Comparative example 1. To the catalyst in example 7, powder of a mixture of tellurium dioxide and silicon dioxide in example 4 in an amount of 2% is added. A fluid bed is formed by passing a mixture of nitrogen and ammonia gases (with an ammonia content of 10% by volume). It is treated at 450 ° C. for 20 minutes. Then, activity studies in the oxidative ammonolysis reaction are carried out. The reaction cannot be continued, since the usually occurring reactions cannot be carried out as a result of generating a large amount of carbon dioxide. Obviously, when processing is carried out in the presence of a gas that has reducing properties (+ inert gas) in the absence of oxygen, the activity decreases noticeably, rather than increases.
    Example 10. Fluidized catalyst of the following empirrg formula
    Fe ,, Mo, „W, Fe., Co3 Ni, Ko ,, 0.3, g (SiO,),
    thirty
    35
    40
    experience in the reaction of oxidative ammonolysis of methanol.
    A gas of the following composition (molar ratio) is introduced into a reactor similar to that used in Example 1, with a resultant relative linear velocity of 15 cm / s: 0 (in the form of air) - methanol 2.10; NH, - methanol 1.20; - methanol 2.00; N - methanol 5.00.
    The reaction is carried out at atmospheric pressure.
    The contact time is determined: similar to example 1.
    When the molar ratio 45 of oxygen to methanol in the source gas decreases, the yield of HCN gradually decreases. Although the molar ratio is reduced to the standard used in the study of activity, the yield of hydrogen cyanide is reduced from 84.1% at the initial stage to 82.6%,
    A mixture of tellurium dioxide and silica dioxide powder is added to this spent catalyst.
    laged way. As a result of this gg, according to Example 4 in an amount of 5%, by the workability, the selectivity for acrylonitrile is increased. The activity of the treated catalyst exceeds the activity of fresh.
    This reaction is again performed. The yield of hydrogen cyanide increases with time, reaching 83.9% after 3 hours.
    five
    0
    five
    Comparative example 1. To the catalyst in example 7, powder of a mixture of tellurium dioxide and silicon dioxide in example 4 in an amount of 2% is added. A fluid bed is formed by passing a mixture of nitrogen and ammonia gases (with an ammonia content of 10% by volume). It is treated at 450 ° C. for 20 minutes. Then, activity studies in the oxidative ammonolysis reaction are carried out. The reaction cannot be continued, since the usually occurring reactions cannot be carried out as a result of generating a large amount of carbon dioxide. Obviously, when processing is carried out in the presence of a gas that has reducing properties (+ inert gas) in the absence of oxygen, the activity decreases noticeably, rather than increases.
    Example 10. Fluidized catalyst of the following empirrg formula
    Fe ,, Mo, „W, Fe., Co3 Ni, Ko ,, 0.3, g (SiO,),
    experience in the reaction of oxidative ammonolysis of methanol.
    A gas of the following composition (molar ratio) is introduced into a reactor similar to that used in Example 1, with a resultant relative linear velocity of 15 cm / s: 0 (in the form of air) - methanol 2.10; NH, - methanol 1.20; - methanol 2.00; N - methanol 5.00.
    The reaction is carried out at atmospheric pressure.
    The contact time is determined: similar to example 1.
    As the molar ratio of oxygen to methanol in the feed gas decreases, the yield of HCN gradually decreases. Although the molar ratio is reduced to the standard used in the study of activity, the yield of hydrogen cyanide is reduced from 84.1% at the initial stage to 82.6%,
    To this spent catalyst, powder of a mixture of tellurium dioxide and silicon dioxide with
    This reaction is again performed. The yield of hydrogen cyanide increases with time, reaching 83.9% after 3 hours.
    7 .13678448
    Example 11. 300 g of catalysis - 1-10 and comparative example 1,
    torus for use in the fluidized bed, the following empirical formula
    , D „8Гг Ыо,„ G., оО7.8 (810)
    thirty
    removed from the reaction medium and kneaded as a thick mass by adding water to it. The resulting mass is molded in the form of cylinders 2 mm long and 2 mm in diameter and dried.
    Using the resulting such
    the catalyst method is used for the reaction of i5 activity, along with the dehydrogenation of butene-1. the results of the study of an active B reactor with an internal diameter of the catalysts themselves. In all cases, 16 mm and a length of 500 mm, 30 ml of tea are loaded with the yield of acrylonitrile below, as well as the catalyst. It is heated in the reaction ban of less than when using molten salt consisting of 20 catalysts activated by equal amounts (mass) mixed by the proposed method, sodium nitrate and nitra with each other. Example 12. Catalyst . Gas is introduced into this reactor with a speedy-designed for use at 7.5 l / h (at normal pressure, fluidized bed, next em- and temperature) gas at mole p-25 pyric formula: air-butene-1 ratio of 5, water - butene-1 is 1.5.
    The reaction is carried out at atmospheric pressure, used in the reaction of oxidative
    At the temperature of the reaction mixture of ammonia of propylene, carried out
    Fe, 0 Sb25Wo ,, 5Fe ,, o06T, 8 (SiO.)
    2 OO}
    At 370 ° C., the degree of conversion of butene-1 is 94%, and the yield of butadiene is 82%. As the temperature of the reaction mixture increases, the amount of carbon dioxide increases, and the excess of oxygen becomes zero. Therefore, under such conditions, the reaction should stop. Although the temperature is then reduced to 370 ° C in order for the reaction to start again, the degree of conversion of butene-1 becomes 91%, and the yield of butadiene corresponds to 78%.
    The catalyst worked out during the reaction is recovered. To this is added the previously obtained granules of tellurium dioxide — silicon dioxide (which are obtained by molding the powder according to Example 4) in an amount of 5% of the amount of catalyst, after which the above reaction is carried out again.
    3 hours after the start of the reaction, the degree of conversion of butene-1 becomes 92%, and the yield of butadiene is 80%.
    The reaction conditions and the results obtained in the examples.
    are given in table. one.
    The surface concentration of tellurium is given in table. 1, measured by x-ray photoelectron spectroscopy. Measurements were made using a PH1-550 instrument. Samples were applied to a copper strip.
    When using catalysts enriched in tellurium (1 mixture of tellurium and molybdenum), which are solid products enriched in tellurium, the results of the studies of the catalysts themselves. In all x, the yield of acrylonitrile is lower, the reaction rate is less than in the case of the catalysts, activated by the proposed method, Example 12. The catalyst used is for the fluidized bed, the following formula
    Fe, 0 Sb25Wo ,, 5Fe ,, o06T, 8 (SiO.)
    2 OO}
    similar to example 1.
    The catalyst activity is reduced by decreasing the molar ratio of oxygen to propylene during the reaction. At the same time, the yield of acrylonitrile decreases from 80.3 to 76.1% -.
    When carrying out the reaction on the catalyst, the resulting
    mixing with 1% of the initial catalysis, a torus of a solid product containing 38.3% tellurium, 2.9% molybdenum and 47.8% silica, the yield of acrylonitrile after 2 hours is equal to 80.5%. Thereafter, the reaction is carried out for another 3 hours, however, the yield of acrylonitrile does not change.
    Example 13. The reactor for carrying out the reaction in a fluidized bed.
    A layer with an inner diameter of 20 cm is filled with a catalyst for use in a fluidized bed layer with the following empirical formula
    55
    Fe, 0 Si, Mo „, UW, Te ,, 5, 4 (SiO).
     60
    and the oxidative ammonolysis of propylene is carried out.
    Relative linear velocity
    1.8 cm / s; the pressure in the reactor is 0.5 kg / cm; molar ratio in the production gas: air - propylene 10.5; ammonia propylene 1.05; reaction temperature 450 ° C.
    When the reaction is carried out for 500 hours under the conditions described, the yield of acrylonitrile is reduced.
    In the study of spent catalyst activity in Example 1, it was found that the yield of acrylonitrile is 83.0%.
    To this catalyst, 1% of the total amount of solid product containing tellurium and molybdenum is added,%: tellurium 35.2; molybdenum 7.9; silicon dioxide 44,0, after which the reaction is continued. Two hours after the solid product containing tellurium and molybdenum is added to the catalyst, the yield of acrylonitrile is 85.5%,
    Example of a spent catalyst of example 13, 1.7% of the total amount of catalyst of the solid product containing tellurium and molybdenum is added, as in example 13 and the reaction of oxidative ammonolysis of propylene is carried out as in example 1, 2 hours after the start, the reaction yield acrylonitrile is 85 3%.
    Example 15 In a reaction of oxidative ammonolysis of methanol, a catalyst of the following empirical formula is removed.
    The yield of hydrogen cyanide and the total conversion of methanol increase over time. After 1 h, the yield of g of hydrogen cyanide is 84.3%, and
    ten
    total methanol conversion is 96.5%.
    Example 16, 300 g of catalyst of the following empirical formula
    Fe, o.Sb, 5Wo.2sTe, oOe7,8 (SiO -,) o
    (in example 12) is removed and kneaded in the form of a thick mass by adding water, and then molded in the form
    15 cylinders with a height of 2 mm and a diameter of 2 mm and dried,
    Using the catalyst prepared in this way, the oxidative dehydriro 20 or butene-1 in Example 11 is reacted
    At a reaction temperature of 370 ° C, the total conversion of butene-1 is 94%, and the yield of butadiene is 82%. When the molar ratio of air to butene-1 in the source gas is reduced, the oxygen concentration in the exhaust gas becomes close to zero. Even if after this the molar ratio of air to butene is 1
    30 again results in a standard, appropriate, condition for studying the activity, the total conversion of butene-1 is reduced to 90%, and the yield of butadiene is reduced to 77%.
    After stopping the reaction and cooling the reactor, the spent catalyst is extracted from it. It is mixed with solid granules of the product containing tellurium and molybdenum (granules
    ,;,., K, 04,, b (510.2) 50; 40 by molding the powder according to example 12), c. amount of 0.5% of the total35
    in example 10,
    With a low molar ratio of oxygen to methanol in the source gas, the yield of hydrogen cyanide gradually decreases. Although the molar ratio of components in the gas leads to the initial value, which is standard for measuring activity, the yield of hydrogen cyanide decreases from 84.1 to 82.0% Then, 1.3% of the total amount of the catalyst of the solid product containing 20% of tellurium (consisting,
    th amount of catalyst, after which the reaction is carried out again,
    After reaction for 3 hours, the conversion of butene-1 becomes 80%, and the yield of butadiene is 92%,
    Example 17, Catalyst of the following empirical formula
    50
    Re, о8Ь „С„ „5MoAg Those ,, оО8, с
    (SiO,),
    g 60
    used in the reaction of oxidative ammonolysis of propylene in Example 1, tellurium added from silicon and oxygen to the indicated catalyst), and also 0.15 of the total amount of 0.8% of the total amount of catalysts in the solid, containing 66.7% of a lysator enriched with tellurium (besides containing sulbdenum (32.9% tellurium and 7.4% oxygen molyblosis), dena)
    136784410
    The yield of hydrogen cyanide and the total conversion of methanol increase over time. After 1 h, the yield of g of hydrogen cyanide is 84.3%, and
    total methanol conversion is 96.5%.
    Example 16, 300 g of catalyst of the following empirical formula
    ten
    Fe, o.Sb, 5Wo.2sTe, oOe7,8 (SiO -,) o
    45
    th amount of catalyst, after which the reaction is carried out again,
    After reaction for 3 hours, the conversion of butene-1 becomes 80%, and the yield of butadiene is 92%,
    Example 17, Catalyst of the following empirical formula
    50
    Re, о8Ь „С„ „5MoAg Those ,, оО8, с
    (SiO,),
    g 60
    used in the reaction of oxidative ammonolysis of propylene in Example 1; 0.8% of the total catalyst enriched with tellurium and molybdenum (32.9% tellurium and 7.4% molybdenum) are added to the indicated catalyst
    ten
    11367844
    Although the total conversion of propylene gas is 18 cm / s; the pressure in the reactor is 98.3%, and the yield of acrylonite is 0.5 kg / cmj; the molar ratio of the chemical is .78.0% at the time of the start of the reaction, the source gas: oxygen total conversion is 99.2% and the exit. (in the form of air) - propylene 2.2; acrylonitrile - 78.7% as a result of the activation process.
    Example 18. To the spent catalyst according to example 13 is added a solid product containing tellurium according to example 15 (consisting, in addition to tellurium, of silicon and oxygen) in the amount of 2% of the total amount of catalyst, after which the reaction of oxidative ammonolysis of propylene is carried out Example 1. 3 hours after the start of the reaction, the total conversion of propylene is 96.7%, and the yield of acrylonitrile is 84.7%.
    Comparative example 2. To the spent catalyst according to example 13 is added a solid product containing 66.7% molybdenum (consisting of oxygen in addition to molybdenum) in an amount of 0.15% of the total amount of silicon, 25, drying the mixture by spraying
    and annealing it at 400 ° C for 2 hours. A solid product containing tellurium and molybdenum, according to example 21, is obtained by mixing pre-cooked ammonia - propylene 1,2; reaction temperature 450 ° C.
    When the reaction is carried out for 670 hours under the above conditions, the yield of acrylonitrile decreases, the amount of carbon dioxide produced increases.
     Spent during the reaction, the catalyst is removed. For every 15–2 kg of the indicated catalyst, a solid product containing tellurium and molybdenum is added in the amounts indicated in Table. 3, after which the oxidative ammonolysis of propylene is carried out according to Example 1. The solid products used in examples 19 and 20, containing tellurium and molybdenum, are obtained by mixing each of the starting components with a dioxide sol
    20
    catalyst.
    Acrylonitrile consumption is 83.3%, however, the total conversion of propylene is increased only to 98.1%.
    The amount of iron oxide and antimony oxides increases slightly.
    in carbon dioxide, as well as the amount of hydrogen cyanide and carbon monoxide.
    Comparative Example 3. The reaction is carried out similarly to Comparative Example 2, except that the amount of molybdenum-containing solid product mixed with the catalyst in this case is 0.75% of the total amount of catalyst.
    The yield of acrylonitrile decreases to 81.2%, and the total conversion of propylene becomes 99.2%. The amount of carbon monoxide and hydrogen cyanide produced is greatly increased.
    The conditions and results of testing in examples 12-18 and comparative examples 2 and 3 are given in table. 2
    Examples 19-21. A fluidized bed reaction reactor with an inner diameter of 20 cm is filled with a catalyst for use in the fluidized bed of Example 17, after which the oxidative ammonium reaction of propylene is reacted under the following conditions: the relative linear velocity of the initial gas is
    ten
    gas 18 cm / s; reactor pressure 0.5 kg / cmj molar ratio of the components of the source gas: oxygen (in the form of air) - 2.2 propylene;
    5 silicon, drying the mixture when spraying
    ammonia - propylene 1,2; reaction temperature 450 ° C.
    When the reaction is carried out for 670 hours under the above conditions, the yield of acrylonitrile decreases, the amount of carbon dioxide produced increases.
     Spent during the reaction, the catalyst is removed. For every 15–2 kg of the indicated catalyst, a solid product containing tellurium and molybdenum is added in the amounts indicated in Table. 3, after which the oxidative ammonolysis of propylene is carried out according to Example 1. The solid products used in examples 19 and 20, containing tellurium and molybdenum, are obtained by mixing each of the starting components with a dioxide sol
    0
    five
    0
    five
    0
    five
    with the addition of sources of molybdenum and tellurium and evils of silicon dioxide, drying it by spraying and annealing at 400 ° C for 2 hours.
    The results obtained in the study. activity, are given in table. four.
    Examples 22-28. To 2 kg of spent catalyst in Examples 19-21, a solid product containing tellurium having a composition corresponding to the data in Table 2 is added. 5, after which the oxidative ammonium reaction of example 1 is carried out.
    These solid products containing tellurium are obtained by mixing raw materials — each component with silica sol, drying by spraying, and annealing at 400 ° C for 2 h.
    The results of the activity study are given in table. 6
    Example 29. A fluidized bed reaction reactor with an inner diameter of 20 cm is filled with a catalyst for use in a fluidized bed of the following empirical formula
    Re, o8b "Sio, 5MOAD5Te ,, Obiv.z (510g) yo,
    after which the oxidative ammonolysis of propylene is reacted under the following conditions: relative linear feed gas feed rate of 1.8 cm / s; pressure 0.5 kgf / cm; the molar ratio of components in the source gas: oxygen (in the form of air) is 2.2 propylene; ammonia - propylene 1,1; reaction temperature 450 ° C.
    If the reaction is carried out for 670 hours under the marked conditions, the yield of acrylonitrile decreases and the amount of carbon dioxide produced increases.
    The indicated spent catalyst is removed. 2 kg of it is mixed with a catalyst rich in tellurium, previously obtained under conditions that exclude exposure to moisture, in such an amount that the specified catalyst rich in tellurium is 10% of the spent catalyst used in this process.
    Torah. The reaction is carried out according to example 1
    The output of acrylonitrile gradually increases to 78.1% in 3 hours. When carrying out the reaction using only the spent catalyst according to Example 1, the yield of acrylonitrile is 76.3%.
    Used in these examples, a rich in tellurium catalyst was prepared as follows. Take 1 kg of a catalyst intended for use in the fluidized bed and corresponding to the above empirical formula before it is produced and mixed with a solution of 56 g of telluric acid in 0.27 l of water. After drying at 120 ° C for 5 h, the mixture is annealed at 350 ° C for 2, .h. The content of tellurium in the resulting such a catalyst: catalyst rich in tellurium is 4.4%.
    Example 30. A fluidized bed reaction reactor with an internal diameter of 20 cm was filled with a catalyst for use in a fluidized bed of the following empirical formula
    Fe, o, MOo., Wo, Te ,, jO (SiO ,,),
    after which the oxidative ammonolysis of propylene is carried out under the following conditions: relative line
    on the feed rate of the source gas 18 cm / s; pressure 0.5 kg / cm; The molar ratio of the reactants in the source gas: air - propylene 10.5; ammonia - propylene 1.05; reaction temperature 450 ° C.
    When carrying out the reaction for 500 hours under the described conditions, the yield
    acrylonitrile decreases.
    When extracting a spent catalyst and examining its activity in Example 1, it was found that the yield of acrylonitrile is 83%.
    The spent catalyst is mixed with the previously obtained catalyst, rich in tellurium and molybdenum, in an amount of 5% of the total amount of spent catalyst under conditions that exclude exposure to water, after which the reaction is carried out according to Example 1. After 3 hours, the yield of acrylonitrile becomes 85.3%.
    Enriched with tellurium and molybdenum
    0
    five
    example, get the following way.
    Take 1 kg of spent catalyst, 90 g of powdered metal -. of metallic tellurium is suspended in 220 ml of an aqueous solution of ammonia paramolybdum (containing 10.2 g of molybdenum-containing component in the form of MoO) and added to the resulting slurry by heating with 35% hydrogen peroxide solution, to obtain the result is a homogeneous solution containing molybdenum and tellurium. Water is added to this solution to bring the amount of liquid to 320 ml. Q Then obtained in this way rast-. the thief is added to the spent catalyst.
    The mixture is thoroughly mixed to impregnate the catalyst with a solution. After drying for 16 hours at 120 ° C, the mixture is annealed at 450 ° C for 2 hours. The result is a mixture of molybdenum and tellurium 50
    The catalyst contains 9.9% tellurium and 1.1% molybdenum.
    Example 31. The spent catalyst of example 30 is mixed with the previously obtained rich gg and molybdenum tellurium catalyst in an amount of 3.5% of the total amount of spent catalyst C. conditions that exclude moisture and then the reaction is carried out as in example 1.
    Four hours after the start of the reaction, the yield of acrylonitrile becomes 85.0%.
    Enriched with tellurium and molybdenum, the catalyst is obtained in the following way.
    98 g of powdered metallic tellurium are suspended in 240 ml of an aqueous solution of paramolybdic acid (containing 33.2 g of molybdenum-donor
    the burning component in the form of MoO) ,. whereupon a 35% solution of hydrogen peroxide is added dropwise to the resulting suspension, to obtain

    homogeneous solution containing tellurium 5
    120 ° C
    and molybdenum. Pure water is added to this solution, bringing the amount of liquid to 320 ml. Then the solution is thoroughly mixed with the catalyst (before it is worked out) in example 30, impregnating the catalyst with a solution. After drying for 5 hours, the mixture obtained is annealed at 400 ° C for 2 hours. The catalyst obtained in this way is rich in tellurium and molybdenum and contains 10.3% tellurium and 2.4% molybdenum.
    The conditions and the results of the experiments in examples 29-31 are given in table. 7
    Example 32. The catalyst of the following empirical formula
    20
    25
    an inner diameter of 2.5 cm and a height of 40 cm, is filled with the above catalyst. A gas of the following composition (molar ratio) is introduced into this reactor: Oj (as air) - propylene 2.2; ammonia is propylene 1.1.
    The reaction is carried out at atmospheric pressure.
    During the reaction, the activity decreases due to a decrease in molar oxygen-to-propylene.
    The yield of acrylonitrile is reduced from 78.2% in the initial stage to 76.8%.
    After stopping the reaction, elemental 3Q tellurium (metal powder with a purity of 99.2%) is added to the deactivated catalyst in an amount of 0.05 wt.% By weight of the deactivated catalyst.
    W
    A2
    MOO.5Teo. „C, D„ ,,., (SiO), „:
    prepared as follows.
    73.0 g of electrolytic iron powder is weighed and added gradually to the solution obtained. heating a mixture of 0.59 l of nitric acid (specific gravity 1.38), and 0.74 l of pure water, and completely dissolved in it. Then, 3.8 g of a metallic tellurium powder is added to the resulting solution and dissolved in it. 115 g of copper nitrate are weighed out and dissolved in a solution of iron nitrate. To the resulting iron-tellurium-copper solution was added 2.142 g of silica sol (wt.%). Weigh out 433 g of antimony trisodium and add to the solution. After dissolving 6.2 g of ammonium para-tungstate and 10.5 g of ammonium para-molybdate in 0.5 l of pure water, this solution is added to the suspension. After that, the pH of the resulting suspension is gradually adjusted by adding a 15% aqueous solution of ammonia with stirring. The suspension
    heated for 4 h at 100 ° C. The suspension thus obtained is subjected to drying with stirring. After calcining the obtained globular particles at 200 ° C for 4 hours and at 400 ° C for 4 hours, they are finally calcined at 850 ° C for 3 hours to obtain a catalyst. Thus, the resulting catalyst is used in the propylene ammoxidation reaction:
    Liquefied reactor, 0
    five
    an inner diameter of 2.5 cm and a height of 40 cm, is filled with the above catalyst. A gas of the following composition (molar ratio) is introduced into this reactor: Oj (as air) - propylene 2.2; ammonia is propylene 1.1.
    The reaction is carried out at atmospheric pressure.
    During the reaction, the activity decreases due to a decrease in the oxygen-propylene molar ratio.
    The yield of acrylonitrile is reduced from 78.2% in the initial stage to 76.8%.
    After stopping the reaction, elemental Q tellurium (metal powder with a purity of 99.2%) is added to the deactivated catalyst in an amount of 0.05 wt.% By weight of the deactivated catalyst.
    The catalyst thus treated is used for the reaction of ammoxidation of propylene. As a result, the yield of acrylonitrile after treatment of the catalyst is 77.5%. Q Example 33. The catalyst of the following empirical formula
    Wo ,,,, 5Ь ,, 0 „,, (Sil,) ,,
    (catalyst I) is prepared analogously to example 5 5. I
    A portion of this catalyst is used as a support for the preparation of a catalyst rich in tel
    0
    lurom, i.e. 0.65 g of telluric acid is dissolved in 30 ml of pure water and the resulting solution of telluric acid is added to 100 g of this catalyst. After stirring, the mixture is calcined at 200 ° C for 2 hours and at 400 ° C for 2 hours.
    The empirical formula of the catalyst thus obtained, enriched with tellurium:
    17 Wo, iMOo, sTeo, 5oCu4Fe ,, Sb, 507 ,,, (SiOj
    (catalyst II).
    Catalyst I is used in the propylene ammoxidation reaction as in Example 32. During the reaction, the activity decreases due to a decrease in the molar ratio (oxygen-propylene) of the feed gas. Therefore, the yield of acrylonitrile is reduced from 78.3% in the initial stage to 77.3%. After stopping the reaction, 23 wt.% (29.9 wt.% On a catalyst with reduced activity) of catalyst II are added to the reaction solution. The mixture reacts under the same conditions as described above. As a result, the yield of acrylonitrile is up to 78.5%.
    The results of the experiments in examples 32 and 33 are given in table. eight.
    权利要求:
    Claims (2)
    [1]
    1. The method of activation of tellurium-containing 15.05.81 according to claim 1, of the metal oxide catalyst for 15.02.82 according to claim 2.
    7844 8
    ammonolysis of propylene or methanol and the oxidative dehydrogenation of butene-1, about that. so that, in order to obtain a catalyst with increased activity and selectivity, the tellurium-containing metal oxide catalyst is heated in a gas atmosphere up to 300-500 ° C in the presence of 1Q tellurium-containing solid product containing 0.72-99.2 wt.% tellurium, in an amount of 0.05-29.9 wt.% of the total mass of the catalyst.
    15
    [2]
    2. Method POP 1, characterized in that the tellurium-containing solid product further comprises molybdenum in an amount of 0.4 -. 7.9 wt.% Or use tellurium20. Keeping. A solid product mixed with a molybdenum-containing solid product with a molybdenum content of 66.7 May.
    00
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    about
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    S: 5
    : §
    to
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    0)
    lit
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    -
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    39
    Control
    Before catalyst production
    After making a catalyst
    19 20 21
    32.0 28.0 28.0
    1.1
    8.1
    1367844
    40 Table 3
    460 3.5 78.0 98.3
    0.9 1.0 4.5
    460 460 460 460
    4.0
    .4,0
    4.0
    4.0
    76,397,8
    78,598,7
    77,998,3
    78,598,5
    Table 5
    49.0 63.0 54.8
    0.81 0.92 0.98
    41
    1367844
    Control
    42 Continuation of table 5
    Table 6
    45
    32 Until reduced activity
    After decreasing activity
    After activation (adding elemental tellurium)
    33
    Until reduced activity
    After decreasing activity
    After activation (addition of enriched Te catalyst)
    1367844.
    46 Table 8
    5.5 78.2 97.5
    5.5 76.8
    5.5 77.5 96.8 0.05 99.2
    5.5 78.3 97.7
    5.5 77.3 96.2.
    5.5 78.5 98.0 29.9 0.72
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    同族专利:
    公开号 | 公开日
    KR830009806A|1983-12-23|
    BR8202794A|1983-04-26|
    NL8202012A|1982-12-01|
    ES512235A0|1983-06-01|
    US4709071A|1987-11-24|
    MX162726A|1991-06-20|
    DD210218A5|1984-06-06|
    DD202630A5|1983-09-28|
    GB2163365B|1986-07-30|
    ES519785A0|1984-03-01|
    ES8306607A1|1983-06-01|
    BG50715A3|1992-10-15|
    CA1189844A|1985-07-02|
    US4709070A|1987-11-24|
    GB8522898D0|1985-10-23|
    GB2163365A|1986-02-26|
    DE3217700A1|1982-12-02|
    GB2101004A|1983-01-12|
    AT384558B|1987-12-10|
    US4618593A|1986-10-21|
    KR890003702B1|1989-09-30|
    IT8248402D0|1982-05-13|
    ATA189882A|1987-05-15|
    GB2101004B|1986-07-16|
    IT1154303B|1987-01-21|
    ES8403040A1|1984-03-01|
    FR2505675A1|1982-11-19|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    JP56073144A|JPH0245499B2|1981-05-15|1981-05-15|
    JP57021095A|JPH0245500B2|1982-02-15|1982-02-15|
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