Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Method for preparing paraxylene and isooctane from diisobutene

A technology for diisobutene and p-xylene, which is applied in the fields of isomerization to produce hydrocarbons, chemical instruments and methods, and hydrogenation to produce hydrocarbons, etc. The effect of efficiency

Active Publication Date: 2014-12-17
LANZHOU INST OF CHEM PHYSICS CHINESE ACAD OF SCI
View PDF6 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] To sum up, these documents and patents do not involve simultaneous aromatization and hydrogenation in the same unit to obtain p-xylene and isooctane

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 paraxylene and isooctane from diisobutene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1~6

[0030] Embodiment 1~6 prepares the catalyst used

Embodiment 1

[0031] Embodiment 1 (Cr 2 o 3 ) 0.05 (MgO) 0.01 PD 0.02 (Al 2 o 3 ) 0.92 preparation of

[0032] Prepare the catalyst by impregnation method according to the above metering ratio, dissolve 26.3g of chromium nitrate nonahydrate and 6.4g of magnesium nitrate hexahydrate in 500mL of deionized water, and then add 92g of γ-Al to the solution 2 o 3 The carrier was impregnated with stirring for 24 hours, evaporated to dryness, and then calcined at 600°C in the air for 4 hours; 5.0 g of palladium nitrate was dissolved in 500 mL of deionized water to prepare a solution, and the calcined solid was immersed in the palladium nitrate solution under stirring conditions for 24 hours. Evaporated to dryness, and then calcined in air at 400°C for 4h. At 450°C, pass through hydrogen-nitrogen mixed gas for reduction to obtain the above-mentioned catalyst.

Embodiment 2

[0033] Embodiment 2 (Cr 2 o 3 ) 0.10 (K 2 O) 0.015 Ir 0.01 (Al 2 o 3 ) 0.875 preparation of

[0034] Prepare the catalyst by the sol-gel method according to the above metering ratio, dissolve 350.5g of aluminum isopropoxide in 500mL of absolute ethanol, dissolve 52.7g of chromium nitrate and 3.2g of potassium nitrate in 200mL of deionized water, and drop into isopropoxide under rapid stirring. Aluminum propoxide ethanol solution, adjust the pH to 7 with ammonia water, make the solution into a gel, and become a gel after standing for 24 hours; then calcined in the air at 500°C for 5 hours; take 2.3g of ammonium chloroiridate dissolved in 500mL of deionized water to prepare Solution, the calcined solid is immersed in the ammonium chloroiridate solution under stirring conditions, soaked for 24 hours, dried and calcined in the air at 400°C for 4h, after the calcining is completed, the hydrogen-nitrogen mixture gas is introduced at 450°C for reduction, and the above-mention...

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 discloses a method for highly selectively preparing paraxylene and isooctane from diisobutene. The method comprises the following steps: a catalytic reaction apparatus is filled with an aromatization-hydrogenation difunctional catalyst, a diisobutene material enters reactor to catalyze a bed reaction, and the obtained products are separated by a separation device to obtain isooctane and paraxylene. The reinforcement of a hydrogenation reaction makes a hydrogenation process and an aromatization process simultaneously carried out in the same reactor, so the technology is simplified, and paraxylene and isooctane are produced in a combined manner; and a paraxylene and isooctane product with different proportions can be obtained through control of the catalyst composition, the reaction temperature and a material cycle ratio, and the paraxylene and isooctane product can improve the economic benefit as a basic organic chemical product and a fuel additive.

Description

technical field [0001] The invention relates to the technical field of organic synthesis, in particular to a method for preparing p-xylene and isooctane (Olefin to Paraffin&p-Xylene, OTPX) from diisobutene with high selectivity. Background technique [0002] P-xylene is an important organic chemical raw material, mainly used for the production of ethylene terephthalate (PET), polytrimethylene terephthalate (PTT) and poly(1,4-cyclohexanedimethanol) terephthalate Raw materials of polyesters such as esters (PCT, PETG) are widely used in many fields such as textiles, plastics, electronics, coatings, dyes and pesticides. The global demand for p-xylene has grown rapidly, reaching 28.2 million tons in 2007, increasing to 29.3 million tons in 2008, and further expanding to 31.52 million tons in 2009 (see: Chambor Zhang. p-xylene market and development prospects, chemical industry , 2010, 28(8):21-23). With the development of polyester industry in my country, the demand for paraxyl...

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
IPC IPC(8): C07C5/31C07C9/16B01J23/652C07C5/03B01J23/36C07C15/08
CPCY02P20/52
Inventor 宋焕玲夏春谷朱刚利李品红
Owner LANZHOU INST OF CHEM PHYSICS CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products