Preparation method for ZSM-48 molecular sieve

A molecular sieve and fully mixed technology, which is applied in the field of ZSM-48 molecular sieve preparation, can solve the problems of high price and achieve the effects of cheap raw materials, reduced synthesis costs, and low silicon-aluminum ratio

Active Publication Date: 2015-05-13
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, although the synthesis technology of ZSM-48 molecular sieve is relatively mature, its existing problems are also relatively obvious. In order to obtain ZSM-48 molecular sieve with low silicon-aluminum ratio, expensive templates must be used.

Method used

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  • Preparation method for ZSM-48 molecular sieve

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Weigh 5.0g of sodium hydroxide and 2.0g of sodium aluminate and dissolve them in 300ml of deionized water, then add 15g of 1,6-dibromohexane, 24g of trimethylamine and 45g of ethanol while stirring at room temperature, stir for 0.5 hours, then add 55g white carbon black, after stirring 1.0 hour, move in the airtight stainless steel reactor. It was crystallized at 160° C. for 6 days, and the obtained crystallized product was analyzed as ZSM-48 molecular sieve by XRD.

Embodiment 2

[0035] Weigh 4.8g of sodium hydroxide and 2.0g of sodium aluminate and dissolve them in 320ml of deionized water, then add 15g of 1,6-dibromohexane, 24g of trimethylamine and 40g of ethanol while stirring at room temperature, stir for 0.5 hours, then add 55g white carbon black, after stirring 1.0 hour, move in the airtight stainless steel reactor. Crystallized at 160° C. for 8 days, and the obtained crystallized product was analyzed as ZSM-48 molecular sieve by XRD.

Embodiment 3

[0037] Weigh 4.8g of sodium hydroxide and 1.8g of sodium aluminate and dissolve them in 320ml of deionized water, then add 15g of 1,6-dibromohexane, 20g of trimethylamine and 40g of ethanol while stirring at room temperature, stir for 0.5 hours, then add 55g white carbon black, after stirring 1.0 hour, move in the airtight stainless steel reactor. It was crystallized at 160° C. for 7 days, and the obtained crystallized product was analyzed as ZSM-48 molecular sieve by XRD.

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Abstract

The invention relates to a preparation method for a ZSM-48 molecular sieve. The method comprises the steps of mixing silicon source, aluminium source, alkali, water and template uniformly; crystallizing, filtering, washing, drying and roasting to obtain the ZSM-48 molecular sieve, wherein the template is dibromohexane (DBH), trimethylamine (TMA) and ethanol (ETA); and properly adjusting the amount of the reaction mixture, and thus the ZSM-48 molecular sieve is obtained. Compared with a molecular sieve prepared by a conventional technology, the ZSM-48 molecular sieve synthesized by the method has the characteristics of low synthetic cost.

Description

technical field [0001] The invention relates to a synthesis technology of molecular sieves, in particular to a preparation technology of ZSM-48 molecular sieves. Background technique [0002] In 1983, the patent USP4397827 reported the synthesis of ZSM-48 molecular sieve for the first time. ZSM-48 molecular sieve is a molecular sieve with a ten-ring channel structure, with a pore size of 0.53nm×0.56nm. Pure silicon ZSM-48 molecular sieve has good low-carbon olefin selectivity in the reaction of synthesis gas to olefins, and low silicon-aluminum ratio ZSM-48 molecular sieve has good catalytic performance, which has attracted widespread attention. [0003] At present, the research focus of ZSM-48 molecular sieve is still on its synthesis process. People have been improving the synthesis method through various methods in order to obtain ZSM-48 molecular sieve with low silicon-aluminum ratio and reduce the synthesis cost of the molecular sieve. The synthesis process of the mol...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01B39/04
Inventor 秦波张喜文张志智刘全杰
Owner CHINA PETROLEUM & CHEM CORP
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