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Preparation method of ZSM-5 molecular sieve material, and ZSM-5 molecular sieve material prepared by the method

A technology of ZSM-5 and molecular sieve, which is applied in the direction of molecular sieve catalysts, double decomposition reaction hydrocarbon production, chemical instruments and methods, etc., can solve the problems of limited source of raw materials, complicated preparation process, high cost, etc., and achieve simple process flow, wide sources, low cost effect

Active Publication Date: 2016-04-06
CHNA ENERGY INVESTMENT CORP LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0010] However, the existing methods for preparing ZSM-5 molecular sieve materials with a micro-nano scale structure are still relatively complicated in the preparation process, and the raw materials used in some methods are not widely available and the cost is high

Method used

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  • Preparation method of ZSM-5 molecular sieve material, and ZSM-5 molecular sieve material prepared by the method
  • Preparation method of ZSM-5 molecular sieve material, and ZSM-5 molecular sieve material prepared by the method
  • Preparation method of ZSM-5 molecular sieve material, and ZSM-5 molecular sieve material prepared by the method

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preparation example Construction

[0031] According to the first aspect of the present invention, the present invention provides a kind of preparation method of ZSM-5 molecular sieve material, and the method comprises the following steps:

[0032] (1) refluxing a mixture to obtain a primary gel, the mixture containing a silicon source, an alkali, water and an optional aluminum source;

[0033] (2) The primary gel is mixed with a structure directing agent, and the silicon source is SiO 2 In terms of the aluminum source as Al 2 o 3 Calculated, the base is calculated as an oxide, and the molar ratio of aluminum source, silicon source, base, structure directing agent and water is 0-10 (preferably 1-8): 200: 2-8: 10-20: 10000- 30000;

[0034] (3) the mixture obtained in step (2) is mixed with polyethylene glycol;

[0035] (4) the mixture obtained in step (3) is subjected to hydrothermal crystallization;

[0036] (5) Separating the mixture obtained by hydrothermal crystallization into solid and liquid, drying an...

Embodiment 1

[0065] Add water glass, sodium aluminate, sodium hydroxide and deionized water into a three-necked flask, and stir and reflux in an oil bath at 75°C for 24 hours. Then, tetrapropylammonium bromide was added into the three-necked flask as a structure-directing agent, and the stirring reaction was continued at room temperature (25° C.) for 4 hours. Among them, Al 2 o 3 Sodium aluminate in terms of SiO 2 water glass in terms of Na 2 The molar ratio of sodium hydroxide, tetrapropylammonium bromide and water in terms of O is 5:200:5:15:20000. Next, add polyethylene glycol (the number average molecular weight is 2000, and the weight ratio of polyethylene glycol to water is 1:1) into the three-necked flask, and stir at room temperature (25° C.) for 4 hours to form a uniform sol. The obtained sol was put into a closed reaction kettle, and crystallized at 165° C. for 48 hours. Filter the mixture obtained by crystallization, wash the obtained solid with deionized water at room temp...

Embodiment 2

[0077] Add water glass, sodium aluminate, sodium hydroxide and deionized water into a three-necked flask, and stir and reflux in an oil bath at 75°C for 24 hours. Then, tetrapropylammonium bromide was added into the three-necked flask as a structure-directing agent, and the stirring reaction was continued at room temperature (25° C.) for 4 hours. Among them, Al 2 o 3 Sodium aluminate in terms of SiO 2 water glass in terms of Na 2 The molar ratio of sodium hydroxide, tetrapropylammonium bromide and water in terms of O is 3:200:5:15:20000. Next, add polyethylene glycol (the number average molecular weight is 2000, and the weight ratio of polyethylene glycol to water is 1:1) into the three-necked flask, and stir at room temperature (25° C.) for 4 hours to form a uniform sol. The obtained sol was put into a closed reaction kettle, and crystallized at 165° C. for 48 hours. Filter the mixture obtained by crystallization, wash the obtained solid with deionized water at room temp...

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Abstract

The present invention discloses a preparation method of a ZSM-5 molecular sieve material. The method is as below: first conducting a reflux reaction on a silicon source and an optional aluminum in an alkaline environment to obtain a primary gel; then introducing a structural directing agent and polyethylene glycol to the primary gel; and then conducting thermal crystallization. The present invention also provides a hydrogen-type ZSM-5 molecular sieve and application thereof, and a methanol conversion process. The preparation method of the ZSM-5 molecular sieve can obtain ZSM-5 molecular sieve material with a micro-nano hierarchical structure; and after conversion of the molecular sieve into a into a hydrogen-type molecular sieve after ion exchange, the hydrogen-type molecular sieve as a catalyst shows long service life and high activity. In addition, the method has the advantages of simple process, and wide sources and low cost of raw materials.

Description

technical field [0001] The present invention relates to a preparation method of ZSM-5 molecular sieve material and the ZSM-5 molecular sieve material prepared by said method. The present invention also relates to a hydrogen type ZSM-5 molecular sieve material and its application. The present invention further relates to a Methanol conversion method. Background technique [0002] ZSM-5 molecular sieve is a kind of aluminosilicate molecular sieve material with MFI structure. Due to its unique pore structure, excellent thermal stability and strong acidity, it is widely used in oil refining and chemical reaction processes. [0003] ZSM-5 molecular sieve has a medium microporous structure of 0.5-0.6 nanometers, which is very suitable for shape-selective catalytic reactions, especially in methanol conversion reactions, disproportionation reactions (such as toluene disproportionation reactions) and alkylation reactions (such as toluene alkylation reactions) showed good catalytic e...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B39/40B01J29/40C07C1/20C07C6/06C07C11/02C07C15/02
CPCY02P20/52
Inventor 田大勇孙守理龙俊英秦绍东孙琦
Owner CHNA ENERGY INVESTMENT CORP LTD