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Novel zeolite, and catalyst for use in production of aromatic hydrocarbon which comprises same

A technology for aromatic hydrocarbons and catalysts, applied in the field of new zeolites and catalysts for the production of aromatic hydrocarbons containing them, can solve the problems of product selectivity reduction, product yield reduction, catalyst deactivation, etc., and achieve excellent production efficiency.

Pending Publication Date: 2022-02-01
TOSOH CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

These non-selective reactions often lead to product yield reduction, product selectivity reduction, catalyst deactivation caused by coke precipitation, etc., judging that it is not preferred

Method used

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  • Novel zeolite, and catalyst for use in production of aromatic hydrocarbon which comprises same
  • Novel zeolite, and catalyst for use in production of aromatic hydrocarbon which comprises same
  • Novel zeolite, and catalyst for use in production of aromatic hydrocarbon which comprises same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0087] Amorphous aluminosilicate gel is added to an aqueous solution of tetrapropylammonium hydroxide (hereinafter sometimes abbreviated as TPA) and sodium hydroxide, and suspended. MFI-type zeolite was added as a seed crystal to the obtained suspension to prepare a raw material composition. The amount of seed crystals added at this time is relative to the Al in the raw material composition 2 o 3 and SiO 2 The weight of is set to 0.7% by weight. In addition, by-produced ethanol is removed by evaporation.

[0088] The composition of this raw material composition is as follows.

[0089] SiO 2 / Al 2 o 3 Molar ratio = 48, TPA / Si molar ratio = 0.05, Na / Si molar ratio = 0.16, OH / Si molar ratio = 0.21, H 2 O / Si molar ratio = 10

[0090] The resulting raw material composition was sealed in a stainless steel autoclave, and crystallized while stirring at 115° C. for 4 days to obtain a slurry-like liquid mixture. After the crystallized slurry mixed liquid was separated into sol...

Embodiment 2

[0102]The same procedure as in Example 1 was carried out up to the crystallization, washing, and drying operations of the zeolite in an autoclave. Disperse the obtained dry powder in 1 mol / L hydrochloric acid at room temperature, after filtering, wash the solid particles with a sufficient amount of pure water, filter again, and dry at 100°C overnight. After firing at 550°C for 1 hour in air, it was treated with 45% steam at 600°C for 3 hours.

[0103] The obtained powder was dispersed in 1 mol / L hydrochloric acid at 40°C, filtered, and the solid particles were washed with a sufficient amount of pure water, filtered again, and dried overnight at 100°C to obtain zeolite.

[0104] Table 1 shows the measurement results of the obtained zeolite. The obtained zeolite was a 10-membered ring fine-pore zeolite having a framework structure of an MFI-type zeolite, and the average particle diameter measured using TEM was 19 nm.

[0105] The difference spectrum of infrared absorption befo...

Embodiment 3

[0109] The same procedure as in Example 1 was carried out up to the crystallization, washing, and drying operations of the zeolite in an autoclave.

[0110] After firing the obtained dry powder at 550°C under air, disperse the obtained powder in 1 mol / L normal temperature hydrochloric acid, after filtering, wash the solid particles with a sufficient amount of pure water, filter again, and dry at 100°C for one Night.

[0111] The obtained powder was calcined at 550° C. for 1 hour in air, and then treated with 600° C. and 20% steam for 60 minutes.

[0112] Table 1 shows the evaluation results of the obtained zeolite. The obtained zeolite was a 10-membered ring fine-pore zeolite having a skeleton structure of an MFI-type zeolite, and the average particle diameter measured using TEM was 24 nm.

[0113] The difference spectrum of infrared absorption before and after 2,4-dimethylquinoline is adsorbed on the obtained MFI type zeolite is shown in figure 1 (sample amount is 56mg), ...

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Abstract

Provided are: novel zeolite having an extremely small amount of specific Bronsted acid sites on the surface thereof, which is expected to be useful as a catalyst for the aromatization of a non-aromatic hydrocarbon typified by an aliphatic hydrocarbon; and a catalyst for use in the production of an aromatic hydrocarbon, which comprises the zeolite. The zeolite is characterized by satisfying the following requirements (i) to (iii). (i) The zeolite has an average particle diameter of 100 nm or less. (ii) The zeolite is 10-membered ring microporous zeolite. (iii) The amount of the Bronsted acid sites on the outer surface of the zeolite is 0.1 to 10.0 [mu]mol / g.

Description

technical field [0001] The present invention relates to a novel zeolite which is a 10-membered ring fine-pore zeolite having a specific amount of Bronsted acid sites on the outer surface, and a catalyst for producing aromatic hydrocarbons comprising the same, and more specifically relates to a novel zeolite which It is a 10-membered ring fine-pore zeolite that functions as a catalyst for producing aromatic hydrocarbons excellent in the production efficiency of aromatic hydrocarbons by having a specific average particle size and having a small amount of Bronsted acid sites on the outer surface. Background technique [0002] Benzene, toluene, and xylene (hereinafter collectively referred to as aromatic compounds) are obtained in most cases as follows: decompose raw oil (such as naphtha, etc.) obtained through petroleum refining in a thermal decomposition reaction device, and distill or extract The aromatic compound is separated and refined from the obtained thermal decompositi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B39/38C01B39/36B82Y40/00B01J29/70C07C2/42C07C15/02C07C15/04B01J35/00
CPCC01B39/38C01B39/36B82Y40/00B01J29/70C07C2/42C07C2529/70C01P2004/64C01P2002/82C07C15/02C07C15/04C07B61/00Y02P20/52C07C2/76C01B39/40C07C2529/40B82Y30/00B01J29/40B01J35/40B01J35/45B01J21/08C07C2521/08B01J35/23
Inventor 大久保周林智洋石本绫花谷诚
Owner TOSOH CORP