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Mesoporous material and preparation method thereof and synthesis methanol catalyst and preparation method thereof

A mesoporous material, a technology for synthesizing methanol, applied in catalyst supports, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problems of catalyst performance improvement, low heteroatom content, poor thermal stability, etc., and achieve good catalytic activity , Large specific surface area, good thermal stability

Inactive Publication Date: 2011-04-20
YANTAI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The performance of the catalyst prepared by the co-precipitation method is not satisfactory, such as a small specific surface, resulting in a low activity of the catalyst
Due to the limitations of the preparation method itself, it is difficult to significantly improve the performance of the catalyst by the co-precipitation method, and a new catalyst preparation method must be sought
[0003] Mesoporous molecular sieve is a new type of functional material with regular pore structure, and its specific surface area is generally 500m 2 More than / g, the main obstacle of the current mesoporous materials as catalysts is the thin pore wall (2-3nm), poor thermal stability, and easy collapse of the structure; another disadvantage is the low content of heteroatoms (generally less than 20 %), when the content of heteroatoms is high, it is difficult to form a mesoporous material with stable structure. Heteroatom content is the key to its application in the field of catalysis

Method used

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  • Mesoporous material and preparation method thereof and synthesis methanol catalyst and preparation method thereof
  • Mesoporous material and preparation method thereof and synthesis methanol catalyst and preparation method thereof
  • Mesoporous material and preparation method thereof and synthesis methanol catalyst and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0032] Weigh Cu(NO 3 ) 2 ·3H 2 O 2.5g, Zn(NO 3 ) 2 ·6H 2 O 1.5g, Al(NO 3 ) 3 ·9H 2 O 20g, dissolve in 100mL deionized water; Weigh 1g trimethylhexadecylammonium bromide and dissolve in 100mL deionized water, then mix the two solutions under vigorous stirring, adjust the pH value with 1M NaOH aqueous solution to 8.5 and continue stirring for 60 minutes. The resulting slurry material was transferred to a 300 mL stainless steel synthesis kettle, and the temperature was raised to 120 ° C to continue the reaction for 100 hours. After the reaction was completed, it was cooled to room temperature. The material was discharged and washed with a centrifuge for many times. The tube furnace was calcined at 550 °C for 3 hours in an air atmosphere to obtain a solid substance whose specific surface area was 520 m by nitrogen adsorption method (BET method). 2 / g, it has a mesoporous structure determined by XRD, indicating that the prepared material is the mesoporous material of the p...

Embodiment 2

[0036] Weigh Cu(NO 3 ) 2 ·3H 2 O 3g, Zn(NO 3 ) 2 ·6H 2 O 1.5g, polyaluminum chloride (containing Al 2 O 320%) 10g, dissolved in 100mL deionized water; Weigh 2g sodium dodecyl sulfonate and dissolve it in 100mL deionized water, then mix the two solutions under vigorous stirring, and adjust the pH to 7.5, continue stirring for 30 minutes. The resulting slurry material was transferred to a 300mL stainless steel synthesis kettle and heated to 30°C to continue the reaction for 250 hours. After the reaction was over, the material was discharged and washed with a centrifuge for many times. The filter cake was dried at 180°C for 10 hours, and then placed in It was calcined at 250 °C for 90 hours in a tube furnace in an air atmosphere to obtain a solid substance whose specific surface area was 510 m by nitrogen adsorption method (BET method). 2 / g, it has a mesoporous structure determined by XRD, indicating that the prepared material is the mesoporous material of the present in...

Embodiment 3

[0040] Weigh Cu(NO 3 ) 2 ·3H 2 O 0.5g, Zn(NO 3 ) 2 ·6H 2 O 3.5g, polyaluminum chloride (containing Al 2 O 3 20%) 20g, dissolve in 100mL deionized water; Weigh 2g betaine and dissolve it in 100mL deionized water, then mix the two solutions under vigorous stirring, adjust the pH to 10.5 with 1M KOH aqueous solution, and continue stirring for 60 minute. The resulting slurry material was transferred to a 300 mL stainless steel synthesis kettle, and the temperature was raised to 150 °C to continue the reaction for 10 hours. After the reaction was completed, it was cooled to room temperature, and the material was discharged and washed with a centrifuge for many times. It was then calcined at 350°C for 25 hours in a tube furnace in an air atmosphere to obtain a solid substance with a specific surface area of ​​525 m measured by the nitrogen adsorption method (BET method). 2 / g, it has a mesoporous structure determined by XRD, indicating that the prepared material is the meso...

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Abstract

The invention relates to a mesoporous material and a preparation method thereof, and a synthesis methanol catalyst and a preparation method thereof, the mesoporous material is composed of the following components by weight percentage: 1%-30% of CuO, 0.5%-20% of Zn and 50%-98.5% of Al2O3; the preparation method of the mesoporous material comprises the following steps: dissolving soluble salts of cupper, zinc and aluminum in deionized water, uniformly mixing the solution with template agent to form blended solution, adjusting pH value, and then, transferring the blended solution to a reaction kettle to generate blue floccus, washing the floccus with water, and filtering to get filter cakes, drying, baking for 2-100 hours, and getting the mesoporous material; the synthesis methanol catalyst is composed of the following components by weight percentage: 30%-70% of CuO, 15%-40% of Zn and 5%-30% of Al2O3; the preparation method of the synthesis methanol catalyst comprises the following steps: using the mesoporous material as a carrier, depositing the Cu and the Zn on a surface of the carrier by a deposition precipitation method to form the parent substance of the synthesis methanol catalyst, and orderly washing, drying, prilling, roasting and shaping the parent substance to get the synthesis methanol catalyst.

Description

technical field [0001] The invention relates to a mesoporous material and a preparation method thereof, a catalyst for synthesizing methanol and the preparation method thereof, and belongs to the technical field of organic chemical synthesis. Background technique [0002] Cu-Zn-Al 2 o 3 Catalysts are widely used in industrial production processes such as low-pressure methanol synthesis reaction, CO water-gas shift reaction, and methanol steam reforming to produce hydrogen. Larger scale and higher level of automation, Cu-Zn-Al 2 o 3 The performance of the catalyst has put forward higher and higher requirements. The development of high-performance catalysts undoubtedly has extremely huge economic value and social benefits. requirements, the Cu-Zn-Al used 2 o 3 Catalysts are generally prepared by coprecipitation. For example, DD296855 discloses a preparation method for synthesizing methanol catalysts. They co-precipitate aqueous solutions of soluble salts of copper, zinc...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/80B01J32/00C07C31/04
CPCY02P20/52
Inventor 房德仁张慧敏
Owner YANTAI UNIV
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