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

High-dispersity catalyst for chloroethylene synthesis and preparation method and application thereof

A catalyst and high-dispersion technology, applied in the direction of catalyst activation/preparation, catalytic reaction, hydrogen halide addition preparation, etc., can solve the problems of low mass transfer and low gas metal dispersion, achieve high catalytic activity and reduce substrate diffusion effect, good stability

Active Publication Date: 2020-02-04
ZHEJIANG UNIV OF TECH
View PDF7 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] The purpose of the present invention is to provide a highly dispersed catalyst for the synthesis of vinyl chloride and its preparation method and application. The present invention fundamentally solves the shortcomings of low gas metal dispersion and low mass transfer in the supported ionic liquid catalyst system

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
  • High-dispersity catalyst for chloroethylene synthesis and preparation method and application thereof
  • High-dispersity catalyst for chloroethylene synthesis and preparation method and application thereof
  • High-dispersity catalyst for chloroethylene synthesis and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0082] Catalyst preparation:

[0083] 1) Select 9.1 g of silicon carbide carrier and 0.91 g of zirconium boride carrier and mix them mechanically for 3 hours, then calcinate for 2 hours under the condition of nitrogen atmosphere and 200° C., and the obtained solid sample is ready for use.

[0084] 2) Dissolve 0.08g of triphenylmethylphosphine bistrifluoromethanesulfonimide salt and 0.02g of triphenylethylphosphine bromide in 5mL of toluene, stir well, then add the solid sample obtained in step 1) , impregnated for 2 hours, and dried at 180°C for later use. Wherein the mass loading of ionic liquid is 1%.

[0085] 3) Dissolve 0.009g of chloroauric acid in 0.05mL of toluene, stir evenly, add the sample obtained in step 2), dip in an external 0.2kV static electric field for 2h, and dry at 180°C for use. Wherein the mass loading amount of gold element is 0.05%.

[0086] 4) 10.109 g of the solid sample obtained above was re-dispersed in a mixed solution of 50 mL of toluene and 1....

Embodiment 2

[0090] Catalyst preparation:

[0091] 1) Select 2g of titanium carbide carrier and 8g of lanthanum boride carrier and mix them mechanically for 2h, then calcinate for 3h in argon atmosphere and 300°C, and the obtained solid sample is ready for use.

[0092] 2) Dissolve 0.25g triphenylmethylphosphine bistrifluoromethanesulfonimide salt and 0.25g N-pentyl-ethylpiperidinium chloride salt ionic liquid in 5mL nitrogen nitrogen dimethylformamide, stir well , adding the solid sample obtained in step 1), soaking for 3 hours, and drying at 180°C for later use. Wherein the mass loading of ionic liquid is 5%.

[0093] 3) Dissolve 0.103g of ruthenium chloride in 0.5mL of nitrogen-nitrogen dimethylformamide, stir evenly, add the sample obtained in step 2), and immerse in an external 3kV static electric field for 2.5h, and under the condition of 180°C Dry and set aside. Wherein the mass loading amount of ruthenium element is 0.5%.

[0094] 4) 12.5 g of the solid sample obtained above wa...

Embodiment 3

[0098] Catalyst preparation:

[0099] 1) 8 g of zirconium carbide carrier and 2 g of hafnium boride carrier were selected and mixed mechanically for 4 hours, and then calcined for 8 hours in a nitrogen atmosphere at 400° C., and the obtained solid sample was used for later use.

[0100]2) Take 0.4g of 1-propyl-2,3-dimethylimidazole bis-trifluoromethanesulfonimide salt and 0.4g of 1-hexyl-2,3-dimethylimidazole bis-trifluoromethanesulfonimide salt ion The liquid was dissolved in 8 mL of toluene, and after stirring evenly, the solid sample obtained in step 1) was added, soaked for 4 hours, and dried at 180°C for later use. Wherein the mass loading of ionic liquid is 8%.

[0101] 3) Dissolve 4.53g of copper phthalocyanine in 9.1mL of toluene, stir evenly, add the sample obtained in step 2), dip in an external 3kV static electric field for 3h, and dry at 180°C for later use. Wherein the mass loading of copper element is 5%.

[0102] 4) 14.81 g of the solid sample obtained above ...

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 high-dispersity catalyst for chloroethylene synthesis and a preparation method and application thereof. The disadvantages that in a supported ionic liquid catalyst system, gasmetal dispersity is not high, and mass transfer is low are avoided fundamentally. Metal in a mixed carrier composed of a carbide carrier and an amorphous carbon carrier of the catalyst is better in dispersion effect, higher in catalytic activity and better in stability, the metal is stabilized on the outer surface layer of the catalyst in the form of coordinating with ionic liquid, the influenceof mass transfer is reduced, and meanwhile the dispersity of the metal is improved; in addition, an additional static electric field is introduced into preparation of the metal-based catalyst loaded with the ionic liquid for the first time, and enrichment of metal active centers on the surface layer of the ionic liquid is promoted; and the metal active centers of the catalyst are distributed on the surface layer of the ionic liquid, thus the influence of substrate diffusion is reduced, and under the evaluated reaction condition, the induction period of the catalyst disappears.

Description

[0001] (1) Technical field [0002] The invention relates to a high-dispersion catalyst for vinyl chloride synthesis, its preparation method and application. [0003] (2) Background technology [0004] Vinyl chloride is the monomer of polyvinyl chloride (PVC), one of the five largest synthetic resins in the world, and is mainly produced by the calcium carbide acetylene method and the petroleum ethylene method. China's coal-rich, oil-poor, and gas-poor energy reserves determine that the calcium carbide acetylene method will continue to be the main process for the production of vinyl chloride in my country for a long time to come, that is, mercuric chloride catalyzes the reaction of acetylene and hydrogen chloride to produce vinyl chloride. However, the highly toxic mercuric chloride catalyst seriously pollutes the environment and endangers human health. Therefore, the development of non-mercury catalysts is very necessary for the sustainable development of the calcium carbide a...

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): B01J31/02B01J31/22B01J31/24C07C17/08C07C21/06B01J37/34B01J37/02
CPCB01J31/0292B01J31/0284B01J31/0279B01J31/0282B01J31/0288B01J31/182B01J31/1815B01J31/1805B01J31/24B01J31/183C07C17/08B01J37/342B01J37/0203B01J37/0207B01J37/0205B01J37/0209B01J2531/18B01J2531/821B01J2531/16B01J2531/822B01J2231/32C07C21/06Y02P20/54
Inventor 李小年赵佳王柏林丰枫许孝良岳玉学邵淑娟朱文锐庞祥雪
Owner ZHEJIANG UNIV OF TECH