Unlock instant, AI-driven research and patent intelligence for your innovation.

Method for preparing isopropylbenzene, isopropylbenzene and preparation method of epoxypropane

A technology of cumene and oxidation state, which is applied in the field of hydrogenolysis of tower reactor materials to generate cumene, can solve the problems of poor catalyst performance, low initial selectivity of cumene, and high initial activity, so as to prevent performance deterioration. , maintain stable activity and selective effect

Pending Publication Date: 2021-03-30
CHINA PETROLEUM & CHEM CORP +1
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Aiming at the defects of the prior art, the present invention uses a special process to treat the α, α dimethyl benzyl alcohol hydrogenolysis catalyst, which solves the problem of α, α dimethyl benzyl alcohol hydrogenolysis used in the existing cumene production technology The technical problem that the high initial activity of the catalyst leads to the low initial selectivity of cumene and the deterioration of the catalyst performance

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing isopropylbenzene, isopropylbenzene and preparation method of epoxypropane
  • Method for preparing isopropylbenzene, isopropylbenzene and preparation method of epoxypropane
  • Method for preparing isopropylbenzene, isopropylbenzene and preparation method of epoxypropane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0087] Mix 1 liter of alumina carrier with 2000 g of chloropalladium acid aqueous solution containing 3.0 g of palladium, dry at 110° C. for 8 hours, and roast at 450° C. for 4 hours to obtain the oxidized palladium-based catalyst precursor. Its main composition is shown in Table 1. The above-mentioned oxidized palladium-based catalyst precursor was reduced in stages with hydrogen, and the specific reduction methods and steps are shown in Table 2.

[0088] Carry out the hydrogenation operation that contains α, the hydrocarbon material of α-dimethylbenzyl alcohol (as shown in Table 1) in continuous mode, described material and hydrogen carry out contact reaction at catalyst bed layer, and the operating condition of reactor is as follows:

[0089] Reaction temperature: 150°C

[0090] Reaction pressure: 1.5MPa

[0091] Fresh oil volume space velocity: 1.5h -1

[0092] Liquid circulation ratio: 4

[0093] Hydrogen / fresh oil volume ratio: 500

[0094] The average results of t...

Embodiment 2

[0096] Mix 1 liter of alumina carrier with 2000 g of chloropalladium acid aqueous solution containing 3.0 g of palladium, dry at 110° C. for 8 hours, and roast at 450° C. for 4 hours to obtain the oxidized palladium-based catalyst precursor. The specific composition of the catalyst is shown in Table 1.

[0097] Put the above-mentioned oxidized palladium-based catalyst precursor in a liquid environment of α,α-dimethylbenzyl alcohol and cumene, wherein the ratio of the two is 1:1, and reduce it in stages with hydrogen. The specific reduction methods and steps are shown in Table 2 .

[0098] Carry out the hydrogenation operation that contains α, the hydrocarbon material of α-dimethylbenzyl alcohol (as shown in Table 1) in continuous mode, described material and hydrogen carry out contact reaction at catalyst bed layer, and the operating condition of reactor is as follows:

[0099] Reaction temperature: 150°C

[0100] Reaction pressure: 1.5MPa

[0101] Fresh oil volume space ve...

Embodiment 3

[0106] Mix 1 liter of alumina carrier with 2000 g of chloropalladium acid aqueous solution containing 3.0 g of palladium, dry at 110° C. for 8 hours, and roast at 450° C. for 4 hours to obtain the oxidized palladium-based catalyst precursor. Its main composition is shown in Table 1.

[0107] The above-mentioned oxidized palladium-based catalyst precursor was reduced in stages with hydrogen in a cumene liquid environment. The specific reduction methods and steps are shown in Table 2.

[0108] Carry out the hydrogenation operation that contains α, the hydrocarbon material of α-dimethylbenzyl alcohol (as shown in Table 1) in continuous mode, described material and hydrogen carry out contact reaction at catalyst bed layer, and the operating condition of reactor is as follows:

[0109] Reaction temperature: 150°C

[0110] Reaction pressure: 1.5MPa

[0111] Fresh oil volume space velocity: 1.5h -1

[0112] Liquid circulation ratio: 4

[0113] Hydrogen / fresh oil volume ratio: 50...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a method for preparing isopropylbenzene, the isopropylbenzene and a preparation method of epoxypropane. The isopropylbenzene is prepared by the following steps: introducing a hydrogen / nitrogen mixed gas to carry out sectional reduction on a catalyst bed layer; and in the presence of hydrogen, making a hydrocarbon material containing alpha,alpha-dimethylbenzyl alcohol contactwith the catalyst bed layer subjected to sectional reduction to obtain isopropylbenzene. The epoxypropane is prepared by the following steps: preparing cumyl hydroperoxide by taking the isopropylbenzene as a raw material; in the presence of a catalyst, enabling the cumyl hydroperoxide to be in contact with propylene for reaction; and conducting rectifying and separating to obtain an epoxypropaneproduct and a hydrocarbon material containing alpha,alpha-dimethyl benzyl alcohol. The preparation method of isopropylbenzene is used for treating a hydrocarbon material containing alpha,alpha-dimethyl benzyl alcohol to obtain isopropylbenzene for recycling. The method provided by the invention solves the technical problems that Cu-Cr and Ni-Cr catalysts used in the existing cumene production technology pollute the environment, the initial selectivity of cumene is not high, and the low-temperature activity of the catalyst is not high.

Description

technical field [0001] The present invention relates to the method for preparing cumene, and the method for utilizing cumene to synthesize propylene oxide, in particular, relates to the reaction of cumene hydroperoxide and propylene to prepare propylene oxide product after separation of propylene oxide by rectification The method for generating cumene by hydrogenolysis of the tower still material. Background technique [0002] Propylene oxide (PO) is an important organic chemical raw material, mainly used in the production of polyether polyols, propylene glycol, propylene glycol ether, etc., of which polyether polyols account for about 70% of the consumption. At present, the commercial production methods of PO mainly include chlorohydrin method, co-oxidation method and cumene peroxide recycling method. The cumene peroxide recycling process has the following advantages: the conversion rate and selectivity of the whole process are very high; the product is only PO, which is n...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07C1/22C07C15/085B01J23/44B01J23/89B01J27/16C07D303/04
CPCC07C1/22C07C15/085B01J23/44B01J23/8926B01J23/8913B01J27/16B01J23/002C07D303/04C07C2523/44C07C2523/89C07C2527/16Y02P20/52
Inventor 赵多刘仲能吕宇皓马文迪顾国耀林渊峰
Owner CHINA PETROLEUM & CHEM CORP