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Post-treatment method for molecular sieve modification

A molecular sieve and modification technology, which is applied in the direction of molecular sieve characteristic silicoaluminophosphate, molecular sieve catalyst, molecular sieve and base exchange compound, etc., can solve problems such as acid loss, uneven distribution of mesopores, collapse of molecular sieve crystal structure, etc., and achieve improved selection The modification method is simple and convenient, and the effect of improving the diffusion rate

Active Publication Date: 2021-06-18
QINGDAO UNIV OF SCI & TECH
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] In order to solve technical problems such as the collapse of molecular sieve crystal structure, acid loss and uneven distribution of mesopores caused by the "top-down" post-treatment method of molecular sieves in the prior art, the present invention provides a molecular sieve modified after-treatment method. Approach

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  • Post-treatment method for molecular sieve modification
  • Post-treatment method for molecular sieve modification
  • Post-treatment method for molecular sieve modification

Examples

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Embodiment 1

[0023] The preparation of the pretreated Beta molecular sieve: first mix and soak the Beta raw powder and pyridine, the mass ratio of the two is 1:20, the soaking time of the Beta raw powder and pyridine is 12h, filter or centrifuge the soaked molecular sieve to obtain molecular sieve powder, and wash with distilled water Remove physically adsorbed pyridine molecules; wash with water and then further dry at 150°C for 2 hours; finally, high-temperature carbonization in a tube furnace at 700°C for 2 hours.

[0024] The pretreated Beta molecular sieve and sodium hydroxide solution (0.4mol / L) were mixed and added into a three-necked flask at a mass ratio of 1:20, and the mixture was dissolved at 70 Heat alkali treatment at ℃ for 2 hours, wash and filter the obtained product several times with deionized water, then dry at 100 ℃ for 5 hours, and roast at 550 ℃ for 5 hours to obtain the modified Beta molecular sieve. Depend on figure 1 (TEM) shows that the distribution of mesopores ...

Embodiment 2

[0035] Preparation of pretreated SAPO-11 molecular sieve: first degass and remove impurities from SAPO-11 raw powder, treat at 100°C for 8 hours; then mix and soak with lutidine, the mass ratio of the two is 1:5, The soaking time of the powder in lutidine is 1h; the soaked molecular sieve is filtered or centrifuged to obtain molecular sieve powder, and washed with distilled water to remove the physically adsorbed pyridine molecules; after washing, it is further dried at 100°C, and the drying time is 12h; finally, high-temperature carbonization in a tube furnace, the carbonization temperature is 300°C, and the carbonization time is 8h.

[0036] Mix the pretreated SAPO-11 molecular sieve with tetrapropylammonium hydroxide (the concentration of lye is 0.1mol / L) according to the mass ratio of 1:5 and add it to the three-necked flask. The mixture solution was heated and alkali-treated at 90°C for 1 hour, the product obtained was washed and filtered several times with deionized wate...

Embodiment 3

[0038] Preparation of pretreated mordenite molecular sieve: first degass and remove impurities from mordenite raw powder, and treat it at 400°C for 1 hour; then mix and soak with aniline, the mass ratio of the two is 1:30, and the mordenite raw powder is soaked in aniline for 24 hours The soaked molecular sieve is filtered or centrifuged to obtain molecular sieve powder, and the pyridine molecules physically adsorbed are washed with distilled water; after washing, the drying temperature is 120 °C, and the drying time is 1 hour; finally, the tube furnace is carbonized at high temperature, carbonized The temperature is 1000°C and the carbonization time is 1h.

[0039] Mix the pretreated mordenite molecular sieve and potassium hydroxide solution (6mol / L) in a mass ratio of 1:20 into a three-necked flask, and put the mixture solution at 50°C under the conditions of microwave power of 600w and magnetic stirring After heating and alkali treatment at low temperature for 12 hours, the...

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Abstract

The invention belongs to the technical field of molecular sieve treatment methods, and discloses a post-treatment method for molecular sieve modification. The post-treatment method comprises the following steps: soaking a molecular sieve in an organic weak base, conducting water washing, drying and carbonizing to obtain a pretreated molecular sieve, and mixing the pretreated molecular sieve with an inorganic base to obtain modified molecular sieve. According to the method, a molecular sieve product with high micropore structure retention degree, high acid site retention degree and a micropore-mesopore structure composite can be obtained; and meanwhile, the post-treatment modification method provided by the invention is simple and convenient, and can achieve the purposes of improving the diffusion rate of macromolecules in molecular sieve crystals and improving the selectivity of a target product.

Description

technical field [0001] The invention relates to the technical field of molecular sieve treatment methods, in particular to a post-treatment method for molecular sieve modification. Background technique [0002] Molecular sieves are a class of porous materials with regular pore structures. Due to their high hydrothermal stability, good shape selectivity, and adjustable acidity, they have been widely used as new materials for catalysis, adsorption separation, and ion exchange. , environment and other related fields. For example, Y-type molecular sieve is the main active component of catalytic cracking unit catalyst in petroleum refining process; A-type molecular sieve is used in gas separation unit to produce oxygen. When molecular sieves are used as catalytic materials, the diffusion of molecules with a molecular size larger than the pores of the molecular sieve will generate resistance, especially when using microporous molecular sieves, high diffusion resistance can easily...

Claims

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Application Information

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IPC IPC(8): C01B39/02C01B39/46C01B39/26C01B39/54C01B37/08B01J29/70B01J29/85B01J29/18B01J35/10
CPCC01B39/026C01B39/46C01B39/26C01B39/54C01B37/08B01J29/7007B01J29/85B01J29/18C01P2006/12C01P2006/14B01J35/615B01J35/633
Inventor 刘毓翔于海刘新春李露刘仕伟刘悦于海龙于世涛
Owner QINGDAO UNIV OF SCI & TECH
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