Carbon dioxide methanation catalyst and preparation method thereof

A technology for methanation catalyst and carbon dioxide, applied in the field of nickel-based carbon dioxide methanation catalyst and preparation thereof, can solve the problems of many by-products, no report on methanation catalyst, etc., and achieves mild process conditions, low cost and wide application range. Effect

Inactive Publication Date: 2010-07-14
SHANXI UNIV
4 Cites 59 Cited by

AI-Extracted Technical Summary

Problems solved by technology

The disadvantage is that there are many by-products, including CO and C 2 h 6 Wait
[0006] So...
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Abstract

The invention discloses a carbon dioxide methanation catalyst and a preparation method thereof. The carbon dioxide methanation catalyst takes an aerogel oxide as a vector, an additive is added, nickel is used as an active component, the additive is alkali metal or alkali earth metal, and the aerogel oxide vector is silicon dioxide, titanium dioxide, zirconium dioxide, aluminum oxide or a compoundthereof. The catalyst comprises the following components in percentage by weight: 5-40wt.% of nickel and 0.01-30wt.% of the additive. The catalyst of the invention has high catalytic activity and stability, and can effectively catalyze carbon dioxide to be hydrogenated into methane at normal pressure under the reaction conditions that the air speed is 2000-20000h<-1>, the ratio of H2 to CO2 is 4:1, and the temperature is 300-500 DEG C. The maximum conversion rate of CO2 is higher than 90% and the maximum selectivity of CH4 is 99.9%. The preparation method of the catalyst of the invention has the advantages of simplicity, easy operation, lower cost and certain application prospects.

Application Domain

Technology Topic

Examples

  • Experimental program(10)

Example Embodiment

[0022] Example 1:
[0023] 1) Ni-Mg/SiO 2 Catalyst preparation
[0024] Weigh 5.8635g nickel nitrate hexahydrate and 0.4161g magnesium nitrate hexahydrate in a beaker, add water to dissolve and dilute to a 50ml volumetric flask to obtain a nickel-magnesium mixed solution. Weigh 3.0g SiO 2 Put the aerogel carrier in a clean evaporating dish, pipette 22.5ml of the mixed solution of nickel and magnesium into the beaker, then pour it into the evaporating dish at one time to soak the carrier, stir quickly for 0.5h, and then let it stand for half an hour. Put it in a blast oven and dry at 100℃ for 3h and 160℃ for 3h, then put it into a muffle furnace and roast it at 500℃ under flowing air atmosphere for 5h to decompose the salt. 2 Reducing treatment at 400℃ in the flow for 3h, after being cooled to room temperature, oxygen passivation to obtain 15%Ni-0.5%Mg/SiO 2 catalyst. After tableting and sieving, particles with a particle size of 40-60 meshes are taken for later use.
[0025] 2) Evaluation of catalyst activity
[0026] Weigh 0.2g of 15%Ni-0.5%Mg/SiO with a particle size of 40~60 mesh 2 The catalyst is loaded into a fixed-bed reactor, using 30ml/min of H at 400℃ 2 After online heating and reducing for 1h, pass in H 2 /CO 2 4/1 (volume ratio) mixed reaction gas, at a reaction temperature of 300~500℃, a reaction pressure of 0.1MPa, and a space velocity of 5000h -1 Under the conditions, temperature programmed reaction, the product is analyzed and detected by gas chromatography. CO at 400℃ 2 The conversion rate reached the maximum, 58.3%, at this time CH 4 The selectivity is 99.5%.

Example Embodiment

[0027] Example 2:
[0028] Weigh 5.8984g nickel nitrate hexahydrate and 0.8371g magnesium nitrate hexahydrate, imitate the catalyst preparation method of Example 1, to obtain 15% Ni-1% Mg/SiO 2 Catalyst for CO 2 Evaluation of methanation activity. CO at 400℃ 2 The conversion rate reached the maximum, 91.7%, at this time CH 4 The selectivity is 99.9%.

Example Embodiment

[0029] Example 3
[0030] Weigh 6.3522g nickel nitrate hexahydrate and 6.3105g magnesium nitrate hexahydrate, imitate the catalyst preparation method of Example 1, to obtain 15%Ni-7%Mg/SiO 2 Catalyst for CO 2 Evaluation of methanation activity. CO at 440℃ 2 The conversion rate reached the maximum at 62.8%, at this time CH 4 The selectivity is 99.0%.
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PUM

PropertyMeasurementUnit
Particle size40.0 ~ 60.0mesh
tensileMPa
Particle sizePa
strength10

Description & Claims & Application Information

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