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

Alkyl arene isomerizing method

A technology for isomerization of aromatics and alkylaromatics, applied in the field of isomerization of alkylaromatics, to achieve the effect of increasing yield

Active Publication Date: 2014-05-28
CHINA PETROLEUM & CHEM CORP +1
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The ethylbenzene conversion rate of this catalyst can reach up to 60%, which still needs to be further improved

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
  • Alkyl arene isomerizing method
  • Alkyl arene isomerizing method

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0021] The preparation method of the catalyst of the present invention is as follows: first mix the sodium-type high-silicon five-membered ring zeolite and / or mordenite with the binder evenly, and add 20-80% of the total mass of the mixed powder, preferably 30-60% The dilute nitric acid is kneaded, shaped and dried, and the concentration of the dilute nitric acid is 1-5% by mass, preferably 1.5-3.5% by mass. The shaped and dried solid is calcined in air at 470-650°C, preferably 500-600°C. Then exchange the sodium ions with ammonium salt solution, filter, wash, dry and roast to obtain the catalyst. The ammonium exchange temperature is 25-120°C, preferably 85-100°C. The ammonium salt used for ammonium exchange is preferably ammonium chloride or ammonium nitrate, and its concentration is 1 to 30% by mass, preferably 3 to 10% by mass.

[0022] The ammonium-exchanged solid is impregnated with a water-soluble compound solution containing Group VIII metals to introduce Group VIII m...

example 1

[0026] (1) Preparation of carrier

[0027] Take SiO 2 / Al 2 o 3 ZSM-5 and alumina powder with a molar ratio of 140 were mixed at a dry basis mass ratio of 70:30. Add 40% of the total mass of the powder with a concentration of 2% nitric acid aqueous solution, knead and knead, dry at 120°C for 2 hours, and roast in air at 600°C for 3 hours to obtain a carrier, which contains 9.5% by mass of ZSM-5 and 30.5% by mass of alumina .

[0028] (2) Preparation of catalyst

[0029] Get the carrier that 100 grams (1) step makes, use the NH that concentration is 3.0 mass % 4 The Cl aqueous solution was ion-exchanged at 80°C for 2 hours, and the obtained solid was washed with deionized water until there was no Cl in the solution. -, then with chloroplatinic acid solution by liquid / solid volume ratio of 2: 1 ratio of immersion for 12 hours, the platinum content in the chloroplatinic acid solution should make the platinum content in the final catalyst be 0.04 mass % (based on the carri...

example 2

[0031] (1) Preparation of carrier

[0032] Take SiO 2 / Al 2 o 3 ZSM-5 with a molar ratio of 60, SiO 2 / Al 2 o 3 The mordenite and alumina powders with a molar ratio of 12 were mixed uniformly at a dry basis mass ratio of 40:3:57. Add 40% of the total mass of the powder with a concentration of 2% nitric acid aqueous solution, knead and knead, dry at 120°C for 2 hours, and roast in air at 600°C for 3 hours to obtain carrier B, which contains 40.2% by mass of ZSM-5 and 2.9% by mass of mordenite %, alumina 56.9% by mass.

[0033] (2) Get 100 grams of the carrier prepared in step (1), carry out ammonium exchange and load platinum according to the method of step 1 (2) of Example 1, and prepare catalyst B, whose platinum content is 0.04% by mass.

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

An alkyl arene isomerizing method comprises adding 0.1-15 wt% of the total charging amount of C9+aromatic hydrocarbons and / or 1.1-4.5 wt% of the total charging amount of toluene to a C8 arene isomerizing raw material and performing an isomerization reaction in the presence of an isomerizing catalyst. The method provided by the invention can effectively prevent the alkyl arene from converting into other substance during the isomerization process and raise the yield of alkyl arene in the resultant.

Description

technical field [0001] The invention is an isomerization method of alkyl aromatic hydrocarbons, specifically, a method for isomerizing ortho- and meta-position alkyl aromatic hydrocarbons into para-position alkyl aromatic hydrocarbons. Background technique [0002] In petrochemical production, C obtained from various processes 8 Aromatics, in addition to p-, m-, and o-xylene, also contain ethylbenzene. Using this as a raw material, pure p-xylene products can be obtained through operations such as isomerization, rectification and adsorption separation. Since the boiling points of ethylbenzene and xylene are very close, separation by rectification requires high energy consumption, low efficiency, and great difficulty. Therefore, the method of ethylbenzene conversion is often used to avoid the accumulation of ethylbenzene in the recycle stream of the combined unit. There are two methods for the conversion of ethylbenzene, one is to convert to xylene through isomerization, and...

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 Patents(China)
IPC IPC(8): C07C5/27C07C15/08B01J29/42
CPCY02P20/52
Inventor 刘中勋梁战桥周震寰阮迟顾昊辉赵斌
Owner CHINA PETROLEUM & CHEM CORP