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Title:
AMMONIA OXIDATION CATALYST COMPRISING ALUMINIUM OXIDE, BISMUTH OXIDE AND MANGANESE OXIDE
Document Type and Number:
WIPO Patent Application WO/1998/025698
Kind Code:
A1
Abstract:
Catalyst claimed to be used to produce nitrous oxide by ammonia oxidation with oxygen. The invention aims at providing catalysts exhibiting a high activity, when oxygen content in reaction mixture is close or lower the stoichiometry one, and high selectivity towards nitrous oxide and low selectivity towards nitrogen oxides. The catalyst composition is as follows, mass.%: manganese oxide (referred to MnO�2?) 5.0-35.0; bismuth oxide 4.5-30.0; aluminium oxide 35.0-90.5; specific surface area is 5-80 m?2�/g.

Inventors:
MOKRINSKII VLADIMIR VASILIEVIC (RU)
SLAVINSKAYA ELENA MARKOVNA (RU)
NOSKOV ALEXANDER STEPANOVICH (RU)
ZOLOTARSKII ILYA ALEKSANDROVIC (RU)
Application Number:
PCT/US1997/020830
Publication Date:
June 18, 1998
Filing Date:
November 12, 1997
Export Citation:
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Assignee:
SOLUTIA INC (US)
MOKRINSKII VLADIMIR VASILIEVIC (RU)
SLAVINSKAYA ELENA MARKOVNA (RU)
NOSKOV ALEXANDER STEPANOVICH (RU)
ZOLOTARSKII ILYA ALEKSANDROVIC (RU)
International Classes:
B01J23/18; B01J23/34; C01B21/22; C01B21/26; (IPC1-7): B01J23/34; C01B21/26; C01B21/22
Foreign References:
US5212137A1993-05-18
US4419274A1983-12-06
Other References:
WERTHER J, HENGER B: "Ermittlung optimaler Betriebseinstellungen für technische Wirbelschichtreaktoren", CHEM. -ING. -TECH, vol. 52, no. 2, 1980, pages 106 - 113, XP002058296
MASSIMILLA L, JOHNSTONE HF: "Reaction Kinetics in fluidized beds", CHEMICAL ENGINEERING SCIENCE, vol. 16, 1961, pages 115 - 112, XP002058297
SHEN CY, JOHNSTONE HF: "Gas-solid Contact in FLuidized Beds", A.I.CH.E, vol. 1, no. 3, March 1955 (1955-03-01), pages 349 - 354, XP002058298
Attorney, Agent or Firm:
Goodman, Kenneth D. (White & Durkee P.O. Box 443, Houston TX, US)
Kraus, Walter (Thomas-Wimmer-Ring 15, M�nich, DE)
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Claims:
CLAIMS:
1. A catalyst for production of nitrous oxide, comprising MnO2, Bi2O3, and Awl203.
2. The catalyst of claim 1, where the catalyst comprises: about 5.035.0 % MnO2; about 4.530.0% Bi2O3; and about 35.090.5% Awl203.
3. The catalyst of claim 1, where the specific surface area of the catalyst is about 580 m2/g.
4. The catalyst of claim 1, where the specific surface area of the catalyst is about 1040 mlg.
5. The catalyst of claim 1, where the catalyst consists essentially of: about 5.035.0 % MnO2; about 4.530.0% Bi203; and about 35.090.5% Al203.
6. The catalyst of claim 1, where the catalyst comprises: about 13 % MnO2; about 11 %Bi2O3;and about 76 % Awl203.
7. The catalyst of claim 1, where the catalyst comprises: about 15 % MnO2; about 15 % Bi2O3; and about 70 % Al203.
8. The catalyst of claim 1, where the catalyst comprises: about 15 % MnO2; about 7.5 % Bi203; and about 77.5 % Awl203.
9. The catalyst of claim 1, where the catalyst comprises: about 10 % MnO2; about 5 % Bi203; and about 85 % Awl203.
10. The catalyst of claim 1, where the catalyst comprises: about 16 % MnO2; about 16 % Bi2O3; and about 68 % A1203.
11. The catalyst of claim 1, where the catalyst comprises: about 5 % MnO2; about 4.5 % Bi203; and about 90.5 % Awl203.
12. The catalyst of claim 1, where the catalyst comprises: about 35 % MnO2; about 30 % Bi2O3; and about 35 % Al203.
Description:
AMMONIA OXIDATION CATALYST COMPRISING ALUMINIUM OXIDE, BISMUTH OXIDE AND MANGANESE OXIDE

The present invention describes catalysts to be used for nitrous oxide production by ammonia oxidation with molecular oxygen in chemical industry.

Along with a high activity, understood as conversion at a definite residence time, catalysts for ammonia oxidation to produce nitrous oxide should also meet the following demands: . they should provide a high selectivity towards nitrous oxide and a low selectivity towards nitrogen oxide in the whole temperature range of ammonia oxidation; they should perform well under conditions, when reaction mixture contains oxygen in stoichiometry amount or below the stoichiometry amount.

As a rule, the known catalysts do not comply with all above demands.

Thus a bulk manganese-bismuth catalyst [1] containing 5% Bi203 and 95% MnO2 has a low activity. At a temperature of 2000C, when the selectivity towards nitrous oxide is maximum, and equals 88.5% at an inlet ammonia concentration of 10.8 vol.% in the oxygen excess, a complete ammonia conversion occurs at a residence time of 5 s. Meanwhile the selectivity towards NO and NO2 is 0.9%. As the process temperature increases to 3000C, the yields of nitrous oxide and NO+N02 are 79 and 3.1% respectively. As ammonia concentration decreases to 3.02 vol.%, the selectivity towards nitrous oxide falls to 65%.

Therefore, beside a low activity in ammonia oxidation by the oxygen excess, the catalyst shows a high selectivity towards nitrogen oxides.

Another catalyst for ammonia oxidation consists of the oxides of iron, bismuth and manganese in the following ratio: 79.45% Foe,03, 11.53% Bi203, 7.21% MnO2 [2]. The maximum yield of nitrous oxide in the said catalyst is 82%, and it is attained under the following conditions: temperature - 3500C; inlet concentrations: ammonia - 10 vol.%, oxygen - 90 vol%. However, at this temperature the selectivity towards nitrogen oxide is 6%. At 3000C the selectivity towards nitrous oxide and nitrogen oxide is 79% and 1.5% respectively.

Therefore, the catalyst does not meet all demands in concern, because it has a low selectivity towards nitrous oxide at a high selectivity towards nitrogen oxide.

Catalyst with a composition of 5% MnO2, 5% Bi2O3, 90% Fe203 [3] is most close in performance and properties to the catalyst claimed in the present invention. It shows the following results. The maximum nitrous oxide yield is 87%, when reaction mixture containing 10% of ammonia in air (thus in oxygen excess, concentration 18.9 vol.%). If reaction mixture contains 1 ammonia part, 5 air parts, and 5 nitrogen parts, and so it is close to stoichiometry (9.1 vol.% ammonia and 9.55 vol.% oxygen), then the yield of nitrous oxide is 81%. At 275-3000C the residence time for complete conversion is 3.6 s. Therefore, the catalyst has a low activity and not high enough selectivity towards nitrous oxide under conditions, when reaction mixture contains ammonia and oxygen in amounts close to stoichiometry.

The present invention aims at providing catalysts that are highly active under conditions, when reaction mixture contains oxygen in amount close or below the stoichiometry one, showing a high selectivity towards nitrous oxide, and a low selectivity towards nitrogen oxide.

For the purpose the claimed catalysts for the nitrous oxide production by ammonia oxidation have the following composition (mass.%): 5.0-35.0 - manganese oxide (referred to MnO2) 4.5-30.0 - bismuth oxide (Bi203) 90.5-35.0 - aluminum oxide (Al203).

The catalysts of the said composition are prepared by impregnating alumina with a solution of Mn and Bi nitrates, or by mixing the powders of Mn and Bi oxides with the powder of aluminum hydroxide to be then molded, or depositing the said components on an inert support. At the final stage the catalysts are dried, and calcined at 375-5500C. Thus obtained catalysts show a high activity, when the oxygen content in the reaction mixture is close or lower the stoichiometry one, and exhibit a high selectivity towards nitrous oxide, and a low selectivity towards nitrogen oxide.

At a temperature of 350"C, and at a residence time of 0.7 sec, ammonia/oxygen ratio being 1.44, and ammonia concentration being 7.3 vol.%, ammonia conversion on the said catalysts is 82-99.2%. The selectivity towards nitrous and nitrogen oxides is 82-84.6 and 2.1 -

2.7% respectively. After water and ammonia separation the final product contains 79.6-81.7% of nitrous oxide, 4.1-5.25% of nitrogen oxide, and 0.82-0.84% of oxygen.

At a temperature of 3000C, and at a residence time of 1.6 sec, ammonia/oxygen ratio being 1.44, and ammonia concentration being 7.3 vol.%, ammonia conversion on the said catalysts is 82.5-99.0%. The selectivity towards nitrous and nitrogen oxides is 83-86 and 0.3- 0.35% respectively. After water and ammonia separation the final product contains 82.2- 84.9% of nitrous oxide, 0.6-0.69% of nitrogen oxide, and 0.75-0.77% of oxygen.

The high activity and selectivity of the claimed catalysts in ammonia oxidation to nitrous oxide is provided by its components at the said percent ratios.

Catalyst specific surface area also has a positive effect. The tests show that at a stable high activity the catalyst shows the highest selectivity, when its specific surface area ranges within 5-80 m2/g.

Example 1. Catalyst with a composition of 13%MnO2/11%Bi203/76%Al203 is prepared as follows. 100 g of alumina granules are impregnated by incipient wetness with a solution of Mn and Bi nitrates, are dried in air and then in a drying chamber at 1 300C for 2-4 h. Thus obtained product is once again impregnated with a solution of Mn and Bi nitrates, dried in air and in the drying chamber at 1 300C for 4 hours. Then the granules were calcined in a furnace at 375-5500C for 2-4 h. Thus obtained catalyst is tested under reaction conditions similar to those described in [3], reaction mixture composition being 9%NH3 and 9%°2 At 3500C and at a residence time of 0.7 s ammonia conversion is 99.2%. Selectivity towards nitrous oxide and nitrogen oxide is 87 and 2.8% respectively. At 3000C at the same gas composition and at a contact time of 1.6 s ammonia conversion is 99.4%. Selectivity towards nitrous oxide and nitrogen oxide is 88.6 and 0.30% respectively. Ssp is 10 m2/g.

Example 2. Catalyst prepared as in example 1 is tested at ammonia to oxygen ratio equal to 1.44 and ammonia concentration equal to 7.3 vol.% in the reaction mixture.

At 3500C and at a residence time of 0.7 s ammonia conversion is 82%. Selectivity towards nitrous oxide and nitrogen oxide is 84.6 and 2.7% respectively. In the final product nitrous oxide to oxygen ratio is 97.4, nitrous oxide to nitrogen oxide ratio being 15.6. After

ammonia and water separation the final product contains 82% of nitrous oxide, 5% of nitrogen oxide, and 0.84% of oxygen.

At 3000C at the same gas composition and at a contact time of 1.6 s ammonia conversion is 82.5%. Selectivity towards nitrous oxide and nitrogen oxide is 86 and 0.35% respectively. In the final product nitrous oxide ratio to oxygen is 110, while nitrous oxide to nitrogen oxide ratio is 121. The final product (after ammonia and water separation) contains 85.2% of nitrous oxide, 0.7% of nitrogen oxide, and 0.78% of oxygen.

Example 3. Catalyst with a composition of 5%MnO2/5%Bi203/Fe2O3 is prepared as described in [3] and tested under the following conditions: reaction mixture composition - 0.75%NH3, 1.5%O2; residence time - 0.072 s, temperature - 350-300°C. At 3500C ammonia conversion is 73%. Selectivity towards nitrous oxide and nitrogen oxide is 76.9 and 3.9% respectively. At 3000C ammonia conversion is 35%. Selectivity towards nitrous oxide and nitrogen oxide is 68 and 1.4% respectively. Ssp is 4 m2/g.

Example 4. Catalyst with a composition of 15%MnO2/15%Bi203/70°/OAI203 is prepared as in example 1 and tested as in example 2. At 3000C ammonia conversion is 38%.

Selectivity towards nitrous oxide and nitrogen oxide is 79 and 1.4% respectively. Ssp is 11 m2/g.

Example 5. Catalyst with a composition of 13%MnO2/11 %Bi203/76%Al203 is prepared as in example 1 and tested as in example 2. At 3500C ammonia conversion is 76%.

Selectivity towards nitrous oxide and nitrogen oxide is 76% and 3.8% respectively. At 3000C ammonia conversion is 39%. Selectivity towards nitrous oxide and nitrogen oxide is 83 and 1.3% respectively.

Example 6. Catalyst with a composition of 15%MnO2/7,5%Bi2O3/77.5%Al2O3 is prepared as in example 1 and tested as in example 2. At 3500C ammonia conversion is 93.2%.

Selectivity towards nitrous oxide and nitrogen oxide is 78.7% and 3.9% respectively. At 300°C ammonia conversion is 58.7%. Selectivity towards nitrous oxide and nitrogen oxide is 80 and 1.2% respectively. Ssp is 11 m2/g.

Example 7. Catalyst with a composition of 10%MnO2/5%Bi2O3/85%Al2O3 is prepared as in example 1 and tested as in example 2. At 350°C ammonia conversion is 92.5%.

Selectivity towards nitrous oxide and nitrogen oxide is 80% and 3.7% respectively. At 3000C ammonia conversion is 62.4%. Selectivity towards nitrous oxide and nitrogen oxide is 77 and 1.3% respectively. Ssp is 11 m2/g.

Example 8. Catalyst with a composition of 16%MnO2/16%Bi203/68%AI203 is prepared as in example 1 and tested as in example 2. At 3500C ammonia conversion is 73%.

Selectivity towards nitrous oxide and nitrogen oxide is 78.8% and 3.9% respectively. At 3000C ammonia conversion is 37%. Selectivity towards nitrous oxide and nitrogen oxide is 37 and 1.4% respectively. Ssp is 39 m2/g.

Example 9. Catalyst with a composition of 5%MnO2/4.5%Bi2O3/90.5%Al2O3 is prepared as follows. 100 g of alumina granules are impregnated by a solution of Mn and Bi nitrates, dried in air and in the drying chamber at 120-13 00C for 4 h. The obtained product was calcined in the furnace in air at 375-5500C for 2-4 h. Thus obtained catalyst was tested as in example 2. At 3500C ammonia conversion is 79%. Selectivity towards nitrous oxide and nitrogen oxide is 76% and 3.6% respectively. At 3000C ammonia conversion is 40%.

Selectivity towards nitrous oxide and nitrogen oxide is 80 and 1.3% respectively. Ssp is 5 m2/g.

Example 10. Catalyst with a composition of 35%MnO2/30%Bi203/35%Al203 prepared mixing a mass containing 52 g of Mn oxide and Bi oxide powders and 35 g of aluminum hydroxide powder with 25 cm3 of water to obtain a moldable paste. Then the paste was molded as cylinder granules 3 mm in diameter, dried at room temperature for 10 h, dried in the chamber at 1200C for 2 h, and calcined in the furnace at 375-5500C for 2-4 h. Thus obtained catalyst was tested as in example 2. At 3500C ammonia conversion is 77%.

Selectivity towards nitrous oxide and nitrogen oxide is 78% and 3.1% respectively. At 3000C ammonia conversion is 39%. Selectivity towards nitrous oxide and nitrogen oxide is 74 and 1.1% respectively. Ssp is 80 m2/g.

References: 1. V.F. Postnikov, L.L. Kuz'min and N.K. Tsal'm,- J.Chem.Ind., 22, 1348 (1937) 2. Zawadzki, Discussions Faraday Soc., 1950, N8, p.140 3. Schlecht, L., and von Nagel, A., Ger. Patent 503200 (1930) Table 1 example content, mass.% conversion, % SN20,% SNO,% TOC MnO2 Bi2O3 1 13 11 99.2 87 2.8 350 99.4 88.6 0.35 300 2 13 11 82 84.6 2.7 350 82.5 86 0.35 300 3 5 5 73 76.9 3.9 350 35 68 1.4 300 4 15 15 38 79 1.4 300 5 13 11 76 76 3.8 350 39 83 1.3 300 6 15 7.5 93.2 78.7 3.9 350 58.7 80 1.2 300 7 10 5 92.5 80 3.7 350 62.4 77 1.3 300 8 16 16 73 78.8 3.9 350 37 74.7 1.4 300 9 5 4.5 79 76 3.6 350 40 80 1.3 300 10 35 30 77 78 3.1 350 39 74 1.1 300