Nickel-based CO hydrogenation catalyst, preparation method therefor and application of nickel-based CO hydrogenation catalyst

A technology of hydrogenation reaction and catalyst, applied in the direction of catalyst activation/preparation, chemical instruments and methods, metal/metal oxide/metal hydroxide catalyst, etc., which can solve the problem of high requirements for reaction equipment, high reaction temperature and complex preparation methods and other problems, to achieve high catalytic activity and stability, high content of active components, and reduce the effect of reaction temperature

Active Publication Date: 2018-11-16
BEIJING INSTITUTE OF PETROCHEMICAL TECHNOLOGY +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Generally, most of the CO hydrogenation reaction catalysts used in industry need to react at a reaction temperature of 280-350°C, so a large amount of high-pressure steam is required to heat the hydrogen-rich gas to the reaction temperature, which not only consumes a large amount of high-pressure steam, but also High requirements on reaction equipment, high operational risk, easy to cause high temperature interlock
[0004] In the prior art, in order to solve these technical problems, Chinese patent CN101607198A disclo

Method used

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  • Nickel-based CO hydrogenation catalyst, preparation method therefor and application of nickel-based CO hydrogenation catalyst
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  • Nickel-based CO hydrogenation catalyst, preparation method therefor and application of nickel-based CO hydrogenation catalyst

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preparation example Construction

[0024] Specifically, the preparation method of the nickel-based CO hydrogenation catalyst may comprise the following steps:

[0025] Step A, prepare a mixed aqueous solution of nickel salt and aluminum salt, and the concentration of nickel salt in the solution is preferably 0.5-1.5 mol / L, so as to obtain a mixed salt solution. Wherein, the nickel salt solution is at least one of nickel nitrate, nickel acetate and nickel sulfate; the aluminum salt solution is at least one of aluminum nitrate and aluminum sulfate. The amount of nickel salt in the mixed salt solution is based on the mass of the methanation catalyst carrier, and is calculated based on the loading of nickel oxide as 55 to 90 wt%; if there is no special description, the loading in this application is The mass percentage calculated based on the mass of the methanation catalyst carrier.

[0026] Step B. According to the ratio of using 2 to 6 times the volume of the first part of the alkali solution per volume of the ...

Embodiment 1

[0038] A nickel-based CO hydrogenation reaction catalyst with a nickel oxide loading of 66% is prepared by the co-precipitation method provided by the present invention, and the preparation method may include the following steps:

[0039] Step A1. Both 59.45 g of nickel nitrate hexahydrate and 58.84 g of aluminum nitrate hexahydrate were dissolved in 150 mL of deionized water to obtain a mixed salt solution.

[0040] Step B1, using a beaker as a reaction vessel, add 20mL of Na in the beaker with a concentration of 2mol / L 2 CO 3 solution and 20mL deionized water, then control the reaction temperature to 75-85°C, and under the stirring condition of 5-20r / s, the concentration of 2mol / L Na 2 CO 3 The mixed salt solution that solution and step A1 make adopts the mode of concurrent flow to join in the described beaker, and control Na 2 CO 3 The molar ratio of the solution to the mixed salt solution is 0.5-5:1, and at the same time, the pH value of the liquid in the reaction vess...

Embodiment 2

[0044] A nickel-based CO hydrogenation reaction catalyst with a nickel oxide loading of 75% is prepared by the co-precipitation method provided by the present invention, and the preparation method may include the following steps:

[0045] Step A2. Both 69.36 g of nickel nitrate hexahydrate and 44.13 g of aluminum nitrate hexahydrate were dissolved in 190 mL of deionized water to obtain a mixed salt solution.

[0046] Step B2, using a beaker as a reaction vessel, add 20mL of Na in the beaker with a concentration of 2mol / L 2 CO 3 solution and 20mL deionized water, then control the reaction temperature to 75-85°C, and under the stirring condition of 5-20r / s, the concentration of 2mol / L Na 2 CO 3 The mixed salt solution that solution and step A2 make adopts the mode of concurrent flow to join in the described beaker, and control Na 2 CO 3 The molar ratio of the solution to the mixed salt solution is 0.5-5:1, and at the same time, the pH value of the liquid in the reaction vess...

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Abstract

The invention discloses a nickel-based CO hydrogenation catalyst, a preparation method therefor and an application of the nickel-based CO hydrogenation catalyst. The nickel-based CO hydrogenation catalyst is prepared from the ingredients, i.e., nickel oxide, aluminum oxide and auxiliaries, wherein the content of the nickel oxide accounts for 55% to 90% the total mass of the nickel-based CO hydrogenation catalyst, and the content of the auxiliaries accounts for 1% to 5% the total mass of the nickel-based CO hydrogenation catalyst; and the nickel oxide has the particle size of 3nm to 17nm. The nickel-based CO hydrogenation catalyst is prepared by adopting a coprecipitation method; through adding the auxiliaries of different kinds, improving an auxiliary adding mode and improving a drying process, the reaction activity of the catalyst is improved, and thus, the reaction temperature of a methanation reaction can be greatly lowered; and very high reaction activity and stability can be maintained under low-temperature conditions, so that the nickel-based CO hydrogenation catalyst can be applied to the complete removal of CO from hydrogen-enriched gases under the low-temperature conditions.

Description

technical field [0001] The invention relates to a CO hydrogenation reaction catalyst, in particular to a nickel-based CO hydrogenation reaction catalyst and a preparation method and application thereof. Background technique [0002] In the industrial installation of naphtha cracking to ethylene, the hydrogen-rich gas separated from the cold box inevitably contains CO and CO 2 , the concentration of CO gas is about 5000ppm, CO 2 The concentration of the gas is about 100ppm. This part of CO gas can poison and deactivate C2, C3 and pyrolysis gasoline hydrogenation catalysts. Therefore, the CO content in the hydrogen-rich gas provided for downstream devices must meet the requirements of hydrogenation catalysts, that is, less than 1ppm. [0003] At present, the methanation method is generally used in the industry to remove CO in hydrogen-rich gas, that is, hydrogenation reaction occurs between CO and hydrogen in hydrogen-rich gas to generate methane that is not toxic to hydrogen...

Claims

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Application Information

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IPC IPC(8): B01J23/83B01J35/10B01J37/03B01J37/34C10G2/00
CPCB01J23/83B01J35/006B01J35/1019B01J35/1047B01J35/1061B01J37/0018B01J37/03B01J37/038B01J37/343C10G2/333
Inventor 张谦温孙锦昌张晋利李兆杰
Owner BEIJING INSTITUTE OF PETROCHEMICAL TECHNOLOGY
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