Unlock instant, AI-driven research and patent intelligence for your innovation.

Preparation method of reaction catalyst for preparing synthesis gas through methane and carbon dioxide dry reforming

A carbon dioxide and catalyst technology, which is applied in the field of preparation of catalysts for the dry reforming of methane and carbon dioxide to synthesis gas, can solve the problems of easy carbon deposition, difficult molding, and easy sintering of catalysts, etc., and achieves increased basic sites, simple preparation methods, and high efficiency. selective effect

Pending Publication Date: 2021-06-01
HENAN ACAD OF SCI +1
View PDF18 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In view of this, the object of the present invention is to provide a method for preparing a catalyst for dry reforming of methane and carbon dioxide to synthesize gas, which can effectively overcome the problems of existing catalysts such as easy sintering, easy carbon deposition, and difficulty in molding.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of reaction catalyst for preparing synthesis gas through methane and carbon dioxide dry reforming
  • Preparation method of reaction catalyst for preparing synthesis gas through methane and carbon dioxide dry reforming
  • Preparation method of reaction catalyst for preparing synthesis gas through methane and carbon dioxide dry reforming

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] 1) 247.78gNi(NO 3 ) 2 ·6H 2 O was dissolved in 250mL deionized water, and then 450g γ-Al 2 o 3 (300°C drying pretreatment for 2 hours) Add to the salt solution to fully infiltrate the carrier. Sonicate for 30 minutes, let stand at room temperature for 3 hours, and then dry at 105°C. Finally, the sample was calcined in an air atmosphere at 600° C. for 4 hours to obtain 514.65 g of catalyst powder.

[0035] 2) Take 400g of the catalyst powder obtained in step 1), add 200g of 30% alkaline silica sol, 25g of sodium aluminosilicate, 30g of turnip powder and 100g of deionized water, mix well, put it dry, and put the mud on the vacuum mud mixer , and then the mixed material is extruded into 3mm strips and cut strips on a piston extruder. After natural drying, it was dried in an oven at 105°C, and finally placed in a muffle furnace at 400°C for 2 hours to obtain a shaped catalyst, which was marked as Catalyst A.

Embodiment 2

[0037] 1) 247.78g Ni(NO 3 ) 2 ·6H 2 O, 77.93g La(NO 3 ) 2 ·6H 2 O was dissolved in 280mL of deionized water, and then 420g of γ-Al 2 o 3(300°C drying pretreatment for 2 hours) Add to the salt solution to fully infiltrate the carrier. Sonicate for 30 minutes, let stand at room temperature for 3 hours, and then dry at 105°C. Finally, the sample was calcined in an air atmosphere at 600° C. for 4 hours to obtain 521.28 g of catalyst powder.

[0038] 2) get 400g step 1) the obtained catalyst powder, add 200g 30% alkaline aluminum sol, 25g water glass, 30g squash powder and 100g H 2 O, mix well, dry, practice mud on the vacuum mud mixer, and then the mixed material is extruded into 3mm strips and cut into strips on the piston extruder. After natural drying, it was dried in an oven at 105°C, and finally placed in a muffle furnace at 400°C for 2 hours to obtain a shaped catalyst, which was marked as Catalyst B.

Embodiment 3

[0040] 1) 247.78g Ni(NO 3 ) 2 ·6H 2 O, 77.50g Ce(NO 3 ) 2 ·6H 2 O was dissolved in 280mL of deionized water, and then 420g of γ-Al 2 o 3 (300°C drying pretreatment for 2 hours) Add to the salt solution to fully infiltrate the carrier. Sonicate for 30 minutes, let stand at room temperature for 3 hours, and then dry at 105°C. Finally, the sample was calcined in an air atmosphere at 600° C. for 4 hours to obtain 523.41 g of catalyst powder.

[0041] 2) Take 400g of the catalyst powder obtained in step 1), add 200g of 30% alkaline aluminum sol, 25g of sodium aluminosilicate, 20g of scallop powder, 5g of ethylene glycol and 90g of deionized water, mix well, dry, and vacuum The mud is practiced on the mud machine, and then the mixed material is extruded into 3mm strips and cut into strips on the piston extruder. After natural drying, it was dried in an oven at 105°C, and finally placed in a muffle furnace at 400°C for 2 hours to obtain a shaped catalyst, which was designate...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention belongs to the technical field of industrial catalyst preparation, and particularly relates to a preparation method of a reaction catalyst for preparing synthesis gas through methane and carbon dioxide dry reforming. The method comprises the following steps: 1) preparation of a powder catalyst: dissolving an active metal soluble salt and an auxiliary agent soluble salt into deionized water, then mixing with solid carrier powder subjected to heating pretreatment by an equivalent-volume impregnation method, and carrying out ultrasonic stirring, standing and aging, drying and roasting to obtain catalyst powder; and 2) catalyst molding: uniformly stirring and mixing the catalyst powder prepared in the step 1) with a binder, an extrusion aid and deionized water, aging, pugging, carrying out extrusion molding, and roasting to obtain the molded catalyst. The preparation method of the reaction catalyst for preparing the synthesis gas through methane and carbon dioxide dry reforming is simple, large-scale preparation is easy, the surface alkaline sites of the formed catalyst are increased, and the catalyst shows excellent catalytic activity and carbon deposition resistance in the reaction for preparing the synthesis gas through methane and carbon dioxide dry reforming.

Description

technical field [0001] The invention belongs to the technical field of industrial catalyst preparation, and in particular relates to a preparation method of a reaction catalyst for synthesis gas produced by dry reforming of methane and carbon dioxide. Background technique [0002] With the rapid development of the global economy, the demand for traditional fossil fuels such as coal and oil in people's life and production is increasing year by year, resulting in energy shortages. The consumption of fossil fuels emits a large amount of greenhouse gases (CH 4 , CO 2 , N 2 O), is one of the main causes of global warming, sea level rise, melting of polar glaciers and frequent occurrence of extreme weather. Methane carbon dioxide reforming technology can convert two greenhouse gases, methane and carbon dioxide, into industrially valuable synthesis gas (CO+H 2 ), and the synthesis gas can be used for the synthesis of long chain hydrocarbons or oxygenated compounds. Methane car...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/755B01J23/83B01J35/10C01B3/40
CPCB01J23/755B01J23/83C01B3/40C01B2203/1058C01B2203/1052C01B2203/1047C01B2203/1041B01J2523/00B01J35/615B01J35/633B01J2523/31B01J2523/41B01J2523/847B01J2523/3706B01J2523/3712B01J2523/842B01J2523/47Y02P20/52
Inventor 肖进彬王文博聂宁刘振张璐璐方玉美任秋鹤王品胜刘晓杰王晓雅
Owner HENAN ACAD OF SCI