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Sulfur-tolerant methanation catalyst and preparation method thereof as well as magnesium aluminate spinel composite carrier and preparation method thereof

A magnesium-aluminum spinel, sulfur-resistant methanation technology, applied in the direction of catalyst carrier, physical/chemical process catalyst, metal/metal oxide/metal hydroxide catalyst, etc., can solve the problem of affecting catalyst high temperature stability and catalyst life Shortening, use performance and production cost can not be achieved, to achieve the effect of improving reaction stability and high temperature catalytic performance stability, improving reaction stability and high temperature catalytic performance stability, improving CO conversion rate and methane selectivity

Active Publication Date: 2017-11-28
CHNA ENERGY INVESTMENT CORP LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, in this application, the aluminum-magnesium spinel precursor and the carrier modifier precursor cannot form a composite porous carrier with a core-shell structure by coprecipitation, kneading or sol-gel methods; Only part of the core-shell structure can be formed, and a considerable proportion of the carrier modifier will enter the pores of the Al-Mg spinel porous carrier instead of the carrier surface, which leads to a very high amount of carrier modifier, reaching 5% -90%, non-core-shell structure or partial core-shell structure will affect the strength of the formed catalyst, which in turn affects the high temperature stability of the catalyst
[0012] That is, the catalytic performance of the sulfur-resistant methanation catalyst disclosed in the prior art has poor high-temperature stability. After the catalyst is used at high temperature for a short period of time, its catalytic performance often deteriorates rapidly, which will lead to shortened catalyst life. At the same time, Raw materials for the production of the above catalysts such as CeO 2 etc. are expensive, therefore, it is impossible to achieve a good balance and balance between performance and production costs.

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  • Sulfur-tolerant methanation catalyst and preparation method thereof as well as magnesium aluminate spinel composite carrier and preparation method thereof
  • Sulfur-tolerant methanation catalyst and preparation method thereof as well as magnesium aluminate spinel composite carrier and preparation method thereof
  • Sulfur-tolerant methanation catalyst and preparation method thereof as well as magnesium aluminate spinel composite carrier and preparation method thereof

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preparation example Construction

[0037] The present invention provides a preparation method of the above-mentioned sulfur-resistant methanation catalyst, comprising:

[0038] (1) providing magnesium aluminum spinel, and using the solution of carrier modifier precursor and magnesium aluminum spinel to prepare the magnesium aluminum spinel composite carrier of core-shell structure;

[0039] (2) Loading the solution of the precursor of the catalyst active component and the solution of the precursor of the optional catalyst promoter onto the magnesium-aluminum spinel composite carrier of the core-shell structure;

[0040] (3) Drying and roasting the product of step (2).

[0041] In the present invention, there is no particular limitation on the source of the magnesium aluminum spinel, which can be prepared by itself or purchased commercially. Therefore, the method for preparing a sulfur-tolerant methanation catalyst of the present invention may also include the step of preparing magnesium aluminum spinel. There...

Embodiment 1

[0077] This example is used to illustrate the preparation of magnesium-aluminum-spinel composite carrier and sulfur-resistant methanation catalyst by co-precipitation-microwave method.

[0078] (1) Preparation of 83Al by co-precipitation method 2 o 3 / 17MgO aluminum magnesium spinel porous carrier

[0079] 311.4g of Al(NO 3 ) 3 9H 2 O and 64.2g of Mg(NO 3 ) 3 ·6H 2 O is jointly dissolved in 500 milliliters of deionized water to form a mixed solution, and the mixed solution and concentrated ammonia water diluted five times (concentration of strong ammonia water is 25wt%) are added into the beaker in parallel at 80° C. and 600 rpm under stirring, and the pH value is maintained at 11.5. After reacting until the precipitation is complete, let stand and age for 12 hours, filter to obtain the precipitate, and wash it with deionized water three times. Put the obtained filter cake in an oven at 120°C for 12 hours to obtain a dry powder. The above dry powder was calcined in a m...

Embodiment 2

[0086] This example is used to illustrate the preparation of magnesium-aluminum-spinel composite carrier and sulfur-resistant methanation catalyst by kneading-microwave method.

[0087] (1) Preparation of 83Al by kneading method 2 o 3 / 17MgO aluminum magnesium spinel porous carrier

[0088] Weigh 300g pseudo-boehmite (Al 2 o 3 content is 70% by weight) is put into the kneader, and the Mg (NO 3 ) 3 ·6H 2 0 and 90 milliliters of deionized water, after mixing evenly, add 12.5g of acidic peptizer nitric acid, make the mixture carry out peptization, then knead for 2h, the mixture shows good plasticity, then the mixture is packed into extruded bars with cylindrical orifices Formed in the machine, the mixture is extruded into a wet bar. After drying the wet strip at 120°C, it was calcined at 700°C for 5 hours in an air atmosphere to obtain a columnar aluminum-magnesium spinel porous carrier, which was analyzed by X-ray fluorescence spectrometer (XRF). The composition of the al...

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Abstract

The invention relates to the field of catalysts, and discloses a sulfur-tolerant methanation catalyst and a preparation method thereof as well as a magnesium aluminate spinel composite carrier and a preparation method thereof. The sulfur-tolerant methanation catalyst comprises a magnesium aluminate spinel composite carrier, a catalyst active component and an optional catalyst aid, wherein the catalyst active component is loaded by the magnesium aluminate spinel composite carrier; the magnesium aluminate spinel composite carrier is a carrier of a core-shell structure formed by a carrier modifier as a shell layer and magnesium aluminate spinel as a core layer; and relative to 100 parts by weight of the magnesium aluminate spinel, the amount of the catalyst aid is 0-20 parts by weight, the amount of the catalyst active component is 5-30 parts by weight, and the amount of the carrier modifier is 2-15 parts by weight. By adopting the sulfur-tolerant methanation catalyst disclosed by the invention, the CO (Carbon Monoxide) transformation rate is increased, the methane selectivity is improved, the reaction stability and the high-temperature catalysis property stability are also improved, the service life of the catalyst is prolonged, and meanwhile the amount of the carrier modifier and the production cost of the catalyst are reduced.

Description

technical field [0001] The invention relates to the field of catalysts, in particular to a sulfur-resistant methanation catalyst and a preparation method thereof, a magnesium-aluminum spinel composite carrier and a preparation method thereof. Background technique [0002] The methanation reaction refers to the reaction of CO in the synthesis gas with H under the action of certain temperature, pressure and catalyst. 2 The process of reacting to form methane. Its reaction formula can be expressed as follows: [0003] CO+3H 2 =CH 4 +H 2 O (1) [0004] CO+H 2 O=CO 2 +H 2 (2) [0005] 2CO+2H 2 =CH 4 +CO 2 (3) [0006] It is generally believed that the methanation reaction of syngas is one of the best solutions for the clean utilization of coal. Syngas is mainly obtained from coal gasification or coal pyrolysis. The synthesis of methane can be achieved by contacting the catalyst. Methanation can not only reduce the greenhouse gas emissions and environmental polluti...

Claims

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Application Information

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IPC IPC(8): B01J21/10B01J32/00B01J23/10B01J23/28B01J23/30B01J23/887B01J35/10C10L3/08
CPCC10L3/08B01J21/005B01J21/10B01J23/005B01J23/10B01J23/28B01J23/30B01J23/8871B01J35/615
Inventor 龙俊英秦邵东杨霞张玉龙孙守理
Owner CHNA ENERGY INVESTMENT CORP LTD
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