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Catalyst for preparing phenol with catalysis distillation and method for preparing phenol

A catalytic distillation and catalyst technology, applied in the preparation of organic compounds, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problems of ineffective use of heat, increased by-products, and many side reactions, etc., to achieve Reduce equipment investment and operating costs, reduce the generation of by-products, and save energy

Inactive Publication Date: 2009-01-14
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The acid-catalyzed decomposition of cumene hydroperoxide in the production process of cumene method to produce phenol has the following problems: (1) sulfuric acid needs to be neutralized with alkali as a catalyst, which consumes acid and alkali and causes pollution, and the equipment must be durable Acid and alkali corrosion, and the process is complicated; (2) a large amount of heat released by the acid-catalyzed decomposition process cannot be effectively utilized, and needs to be drawn out with circulating acetone, and the energy utilization of the process is very unreasonable; (3) the concentration of cumene hydroperoxide is not enough Safe, and more side effects when the concentration is high
The result is that the actual reaction temperature within the catalyst is too high, the by-products increase and the selectivity decreases

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Stir 0.5 mol of diethoxysilane and platinum catalyst at 75°C for 30 minutes, then add 0.5 mol of p-chloromethylstyrene and stir to generate diethoxysilane containing chloromethylbenzene functional groups; diethoxy Silane and p-chloromethylstyrene are added according to the stoichiometric ratio, and the molar ratio of the catalyst to the reactant diethoxysilane is 2×10 -5 Add the diethoxysilane containing functional groups into a three-necked flask, add hydrochloric acid as a catalyst, add deionized water dropwise under stirring, and further hydrolyze at 60°C for 72 hours to generate polysiloxane containing chloromethylbenzene functional groups; raw materials The ratio of polysiloxane and deionized water is 3:1; polysiloxane containing functional groups reacts with magnesium chloride to form polysiloxane metal complexes; polysiloxane metal complexes are further crossed with tetraethylsiloxane under acidic conditions Polysiloxane metal complexes are formed by joint curing...

Embodiment 2

[0036] Catalyst is prepared with embodiment 1. The catalyst is loaded by the mixed packing method, the packing / catalyst is 4, and the feed flow rate is 2×10 -7 m 3 .s -1 , the feed acetone / CHP is 1, the reflux ratio of the rectification operation is 1, the yield of the product CHP is 89.5%, and the purity of the overhead product acetone is 91.5%.

Embodiment 3

[0038] Catalyst is prepared with embodiment 1. The catalyst is loaded by the mixed packing method, the filler / catalyst is 2, and the feed flow rate is 2×10 -7 m 3 .s -1 , the feed acetone / CHP is 4, the reflux ratio of the rectification operation is 1, the yield of the product CHP is 73.4%, and the purity of the top product acetone is >99%.

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Abstract

The invention discloses a catalyst for the preparation of phenol by catalytic rectification and a phenol preparation method thereof, relating to the preparation of a compound. The invention provides a non-porous solid catalyst used to catalyze phenol preparation by catalytic rectification, as well as a phenol preparation method integrated with catalytic reaction and rectification separation by reaction rectification. The catalyst is a resin polysiloxanes metal complex, and the compostion is SiMR, wherein, M indicates metal complex, R indicates organic carbon chain. The process of phenol preparation by catalytic rectification includes: firstly, double helix ring high-efficient filler is filled in the stripping section and the rectification section of the rectifying tower; proper catalyst is filled in the catalytic rectification section and diluted with the same filler at the ratio of 4:1; the main feed CHP inlet is arranged between the rectification section and the reaction section, and the feed CHP is diluted with acetone at the ratio of 1:1; the auxiliary feed acetone inlet is arranged between the stripping section and the reaction section, the feed quantity covers 50-100 percent of the main feed quantity, and the product is collected at the tower top and the tower bottom. The heat of reaction can be applied to rectifying separation.

Description

technical field [0001] The present invention relates to the preparation of a kind of compound, especially the method for preparing phenol by reactive distillation. Background technique [0002] According to statistics, more than 90% of phenol in the world is produced by the cumene method. The process steps are as follows: benzene and propylene are reacted to obtain cumene; cumene is oxidized by oxygen or air to generate cumene hydroperoxide (CHP); CHP is decomposed to generate phenol and acetone. This method is most typical with the phenol method technology of KBR company. In addition to the production of high-purity phenol and acetone from cumene, the by-products α-methylstyrene (AMS) and acetophenone (AP) are also recovered. In this process, the efficiency of cumene to be oxidized to CHP by air is as high as 95%, and CHP is concentrated and decomposed into phenol and acetone with high yield (greater than 99%) in the presence of an acid catalyst. AMS is hydrogenated to c...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J31/06B01J31/26C07C39/04C07C37/08
CPCY02P20/10Y02P20/52
Inventor 刘庆林朱爱梅苏玉忠林丽华
Owner XIAMEN UNIV
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