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Okra type SAPO-34 molecular sieve as well as preparation method and application thereof

A SAPO-34, molecular sieve technology, applied in molecular sieve catalyst, molecular sieve and alkali exchange phosphate, molecular sieve characteristic silicoaluminophosphate and other directions, can solve the problems of long mass transfer diffusion distance, poor mechanical resistance, poor mechanical stability, etc. Achieve long catalytic life, good mechanical stability, and increase the effect of contact area

Active Publication Date: 2021-06-11
XINXIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The molecular sieve prepared by this patent has a small needle-like shape and a short crystal width, which is conducive to shortening the mass transfer distance, but due to its fine size, its mechanical stability may be poor
[0005] In summary, SAPO-34 molecular sieve catalysts with conventional cubic morphology have the problem of long mass transfer diffusion distance, and the lamellar and needle-like morphology have poor mechanical resistance.

Method used

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  • Okra type SAPO-34 molecular sieve as well as preparation method and application thereof
  • Okra type SAPO-34 molecular sieve as well as preparation method and application thereof
  • Okra type SAPO-34 molecular sieve as well as preparation method and application thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0025] Take 0.62mL of phosphoric acid solution and 0.65mL of tetraethyl orthosilicate in a beaker, then add 7.0mL of deionized water into the beaker, stir at 40°C for 1 hour; then gradually add 2.1g of aluminum isopropoxide and 1.3 mL of morpholine solution, stirred at 40°C for 4 hours to obtain synthetic solution A; weighed 1.68g of PVA17-92 and added it to synthetic solution A, and then added 0.61mL of 40wt% hydrofluoric acid solution dropwise; continued heating at 40°C Stir for 2h to obtain the dispersed synthetic solution B. Transfer the dispersed synthetic solution B into a reaction kettle with a polytetrafluoroethylene liner. After the transfer is completed, move the reaction kettle into an oven for hydrothermal crystallization at 180°C for 50 hours. After the hydrothermal crystallization is completed, cool down to room temperature quickly, then filter and wash the sample; collect the sample and dry it in a blast drying oven at 100°C for 10 hours; put the dried sample in...

Embodiment 2

[0027] Take 0.62mL of phosphoric acid solution and 0.67mL of tetraethyl orthosilicate in a beaker, then add 7.0mL of deionized water to the beaker, stir at 40°C for 1 hour; then gradually add 2.1g of aluminum isopropoxide and 1.3 mL of morpholine solution, stirred at 40°C for 4 hours to obtain synthetic solution A; weighed 1.68g of PVA17-92 and added it to synthetic solution A, and then added 0.61mL of 40wt% hydrofluoric acid solution dropwise; continued heating at 40°C Stir for 2h to obtain the dispersed synthetic solution B. Transfer the dispersed synthetic solution B into a reaction kettle with a polytetrafluoroethylene liner. After the transfer is completed, move the reaction kettle into an oven for hydrothermal crystallization at 180°C for 50 hours. After the hydrothermal crystallization is completed, cool down to room temperature quickly, then filter and wash the sample; collect the sample and dry it in a blast drying oven at 100°C for 10 hours; put the dried sample into...

Embodiment 3

[0029] The steps in this embodiment are exactly the same as those in Embodiment 1. The difference is: during the preparation of the synthetic liquid A, the added aluminum isopropoxide was changed from 2.1 g to 2.0 g. The prepared samples also exhibited okra-type SAPO-34 molecular sieves. Its X-ray powder diffraction spectrogram and SEM photograph and embodiment 1 figure 1 and figure 2 resemblance.

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Abstract

The invention discloses an okra type SAPO-34 molecular sieve as well as a preparation method and application thereof. The preparation process mainly comprises the following steps: mixing a phosphorus source, a silicon source, an aluminum source, a template agent and deionized water, and heating and stirring to obtain a synthetic solution A; adding powder polyvinyl alcohol and hydrofluoric acid into the synthetic solution A, and continuously heating and stirring to obtain a dispersed synthetic solution B; and transferring the dispersed synthetic solution B into a high-pressure reaction kettle, carrying out hydrothermal crystallization, and filtering, washing, drying, roasting and cooling the obtained solid product. The prepared SAPO-34 molecular sieve is of a special okra type morphology structure, the particle size length is 3-5 microns, the particle size width is 0.5-1.5 microns, the SAPO-34 molecular sieve is an excellent catalyst carrier due to the special morphology, mass transfer is facilitated due to the flat structure, and the SAPO-34 molecular sieve shows excellent catalytic performance in the methanol-to-olefin catalytic reaction process.

Description

technical field [0001] The invention belongs to the technical field of molecular sieve materials, and in particular relates to an okra-type SAPO-34 molecular sieve and a preparation method and application thereof. Background technique [0002] Due to its special pore structure, SAPO-34 molecular sieve has good shape selectivity to ethylene, propylene and other low-carbon olefins, and as the main catalyst, it shows excellent catalytic activity in methanol to olefins. However, the smaller pores and the conventional cubic shape limit the mass transfer to a certain extent. Studies have shown that the sheet-like shape or flat shape can shorten the diffusion path of reactants and products, inhibit the formation of carbon deposits and prolong the Catalyst service life. [0003] The invention patent of 201610915336.X introduced a preparation method of layered SAPO-34 molecular sieve. The templating agent used in this patent is tetraethylammonium hydroxide, which is used in a relat...

Claims

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Application Information

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IPC IPC(8): C01B39/54C01B37/08B01J29/85C07C1/20C07C11/04C07C11/06
CPCC01B39/54C01B37/08B01J29/85C07C1/20C01P2004/30C01P2004/61C01P2004/62C01P2002/72C01P2004/03C07C11/04C07C11/06Y02P20/52Y02P30/20Y02P30/40
Inventor 李丽张世超崔红志王俊丽梁宇
Owner XINXIANG UNIV