Methanation catalyst taking rutile type TiO2 as carrier and preparation method of methanation catalyst

A methanation catalyst, rutile-type technology, applied in the field of methanation catalyst and its preparation with rutile TiO2 as the carrier, can solve the problems of small specific surface area of ​​titanium dioxide, complex catalyst preparation process, low specific surface area of ​​composite carrier, etc., and achieve good promotion Application potential, low active ingredient content, low production cost effect

Active Publication Date: 2018-07-06
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the disadvantages of small specific surface area, low strength and high cost of titanium dioxide, it is difficult to apply it in industry
Chinese patent CN102091631A discloses a catalyst with alumina-magnesia-titanium oxide as the carrier, cerium oxide as the auxiliary agent, and nickel as the active component. The catalyst is used in the field of coal-to-natural gas and has high activity and thermal stability property; Chinese patent CN102302936A discloses a co-precipitation method to prepare a titanium-containing nickel-based catalyst, the disadvantage of which is that the catalyst preparation process is complicated and the specific surface area of ​​the catalyst is low; Chinese patent CN103157485A discloses a method using TiCl 4 with Al(NO 3 ) 3 Co-precipitation is a method for preparing a titanium-aluminum composite carrier, but the specific surface area of ​​the composite carrier is low, and it needs to be formed in the later stage, so the process is complicated; A mixture of silicon and titanium oxide is used as a carrier catalyst, which can meet the requirements of heat resistance and high temperature resistance in coal-based natural gas; It is a non-uniformly distributed catalyst with mechanical mixing as the carrier, nickel as the active component, magnesium oxide and lanthanum trioxide as auxiliary agents, and has good catalytic activity for low-temperature methanation

Method used

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  • Methanation catalyst taking rutile type TiO2 as carrier and preparation method of methanation catalyst
  • Methanation catalyst taking rutile type TiO2 as carrier and preparation method of methanation catalyst

Examples

Experimental program
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Effect test

Embodiment 1

[0019] 1) Rutile TiO 2 Preparation of vector

[0020] Take 25g of pseudo-boehmite and put it into a kneader, add 200mL of deionized water, use dilute nitric acid at 50-80°C to adjust the pH value to 3-4, and knead to prepare aluminum sol. 500g rutile TiO 2 The powder is added to the prepared aluminum sol, mixed and kneaded into a plastic mass, and then extruded by an extruder. After the formed catalyst carrier is left at room temperature for 4-6 hours, it is dried at 80-120°C for 1-2 hours, and then calcined at 500°C for 4-8 hours;

[0021] 2) Impregnation of the carrier

[0022] Take 116.8g of nickel nitrate and 27.8g of cerium nitrate, add 200g of deionized water to dissolve, adjust the pH value with ammonia water and citric acid, and form a complex solution. Equal volume impregnated rutile TiO 2 carrier. Stand at room temperature for 4-6 hours, then dry at 110°C for 2-4 hours. The dried catalyst was calcined at 550° C. for 4 h in a muffle furnace.

Embodiment 2

[0024] 1) Rutile TiO 2 Preparation of vector

[0025] TiO 2 The preparation of carrier is the same as embodiment 1

[0026] 2) Impregnation of the carrier

[0027] Take 116.8g of nickel nitrate and 26.6g of lanthanum nitrate, add 200g of deionized water to dissolve, adjust the pH value with ammonia water and citric acid, and form a complex solution. Equal volume impregnated rutile TiO 2 carrier. Stand at room temperature for 4-6 hours, then dry at 110°C for 2-4 hours. The dried catalyst was calcined at 550° C. for 4 h in a muffle furnace. .

Embodiment 3

[0029] 1) Rutile TiO 2 Preparation of vector

[0030] TiO 2 The preparation of carrier is the same as embodiment 1

[0031] 2) Impregnation of the carrier

[0032] Take 116.8g of nickel nitrate, 13.9g of cerium nitrate, and 13.3g of lanthanum nitrate, add 200g of deionized water to dissolve, adjust the pH value with ammonia water and citric acid, and form a complex solution. Equal volume impregnated rutile TiO 2carrier. Stand at room temperature for 4-6 hours, then dry at 110°C for 2-4 hours. The dried catalyst was calcined at 550° C. for 4 h in a muffle furnace.

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Abstract

The invention relates to a methanation catalyst taking rutile type TiO2 as a carrier and a preparation method of the methanation catalyst and relates to methanation catalysts. The methanation catalysttaking the rutile type TiO2 as the carrier is prepared from the ingredients in percentage by mass: 2% to 16% of nickel oxide, 75% to 90% of titanium dioxide, 2% to 10% of rare-earth metal oxide and the balance of aluminum oxide. The preparation method comprises the steps: putting pseudo-boehmite and diluted acid into a kneader to prepare an aluminum sol composite binder, then, adding the rutile type TiO2 powder, carrying out kneading to obtain plastic mass, then, carrying out strip extruding forming, carrying out standing, carrying out baking, and carrying out roasting, so as to obtain the rutile type TiO2 carrier; preparing a complexing solution from a soluble nickel salt, a rare-earth metal soluble salt, ammonia water and citric acid, dipping the formed TiO2 carrier; after dipping, carrying out room-temperature standing, and carrying out baking; carrying out heat treatment: subjecting the dipped catalyst to programmed heating roasting, subjecting the nickel salt and the rare-earth metal salt to pyrolysis to obtain oxidation states, thereby obtaining the methanation catalyst taking the rutile type TiO2 as the carrier.

Description

technical field [0001] The invention relates to a methanation catalyst, in particular to a rutile-type TiO mainly used for the low-temperature methanation of a small amount of CO in crude hydrogen 2 Carrier-based methanation catalyst and its preparation method. Background technique [0002] Methanation technology is widely used, not only in the methanation reaction of CO in coal pyrolysis gas, coke oven gas, and biomass pyrolysis, but also in industries such as ammonia synthesis and fuel cells to remove H-rich 2 A small amount of CO in the system to prevent catalyst poisoning. Generally speaking, the CO content in the hydrogen gas is required to be lower than 10ppm in the chemical process, and the CO content is required to be lower in the fuel cell. The hydrogen refining process generally uses a catalytic methanation method to reduce the CO in crude hydrogen to an appropriate range. [0003] At present, the research on methanation reaction catalysts mainly focuses on oxid...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/83B01J37/08B01J37/02C07C1/04C07C9/04
CPCB01J23/83B01J37/0018B01J37/0201B01J37/086C07C1/0435C07C9/04
Inventor 连奕新霍秀春赖伟坤李洪林张杰朱玲婷
Owner XIAMEN UNIV
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