Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of gas phase fluorination catalyst

A technology for phase fluorination catalysts and fluorination catalysts, which is applied in the field of preparation of fluorination catalysts, and can solve the problems of frequent regeneration and activation, reduced specific surface area, and low activity of fluorination catalysts

Active Publication Date: 2018-05-22
RUYUAN DONGYANG LIGHT FLUORIDE CO LTD
View PDF7 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Aiming at the problems in the prior art that the specific surface area of ​​the gas-phase fluorination catalyst precursor undergoes fluorination and activation treatment is greatly reduced, resulting in low activity, poor stability, frequent regeneration and activation of the fluorination catalyst, etc., the present invention provides A new preparation method of gas-phase fluorination catalyst, the obtained gas-phase fluorination catalyst still has a high specific surface area after fluorination, exhibits high activity and high stability, and is especially suitable for the preparation of R134a products

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
  • Preparation method of gas phase fluorination catalyst
  • Preparation method of gas phase fluorination catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1-1

[0071] The preparation of embodiment 1-1 nanocrystalline γ-alumina powder

[0072] 25.03g Al(NO 3 ) 3 9H 2 O, 1.35g MgCl 2 , 0.21gLaCl 3 1. 1g of organic matter I (0.26g of isopropanol + 0.56g of tartaric acid + 0.18g of glucose) was dissolved in 500mL of ethanol solvent, refluxed at 80°C for 2h, then added dropwise with ammonium carbonate aqueous solution for 10min, and then maintained the reaction Crystallize at high temperature for 12 hours to obtain a liquid sol, then vacuum dry the liquid sol at 110°C for 12 hours to obtain a solid gel, and finally roast at 550°C for 3 hours to obtain nanocrystalline γ-alumina powder, which is used as a carrier for future use.

Embodiment 1-2

[0073] The preparation of embodiment 1-2 nanocrystalline gamma-alumina powder

[0074] 25.03g Al(NO 3 ) 3 9H 2 O was dissolved in 500mL ethanol solvent, refluxed at 80°C for 2h, then ammonium carbonate aqueous solution was added dropwise for 10min, and then crystallized at the reaction temperature for 12h to obtain a liquid sol, and then the liquid sol was vacuum-dried at 110°C After 12 hours, a solid gel was obtained, and finally the nanocrystalline γ-alumina powder was obtained by roasting at 550°C for 3 hours.

Embodiment 2

[0075] The preparation of embodiment 2 amorphous chromium oxide powder

[0076] Weigh 50.02g CrCl 3 ·6H 2 O, 1.85gMgCl 2 , 2.81g AlCl 3 , 1.53gZnCl 3 , 0.21g LaCl 3 , 2.49g organic matter I (0.68g ethanol+1.42g citric acid+0.39g sucrose) was dissolved in 900mL deionized water to obtain a mixed salt solution, the mixed salt solution was mixed with ammonia water until the solution pH=10, filtered and washed with water to obtain a sample, The sample was dried in an oven at 110°C for 6 hours, and then transferred to a roasting furnace. 2 Roast at a high temperature of 350°C for 3 hours in the atmosphere, crush and sieve the calcined sample to obtain amorphous chromium oxide powder for future use.

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

PropertyMeasurementUnit
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to View More

Abstract

The invention relates to a preparation method of a gas phase fluorination catalyst. The preparation method comprises the following steps: evenly mixing nano crystal gamma-alumina powder, amorphous chrome oxide powder, an organic matter II, and graphite, pressing and moulding the mixture to obtain a precursor of the gas phase fluorination catalyst; and finally fluorinating the precursor to obtain the gas phase fluorination catalyst. The nano crystal gamma-alumina powder is prepared by a water containing gel-sol method, and an organic matter I is added. The organic matter I and the organic matter II can be heated, decomposed, and volatilized to generate pores so that after fluorination, obtained gas phase fluorination catalyst still has a large specific surface area, high activity, and highstability, and the preparation method is especially suitable for the preparation of a R134a product.

Description

technical field [0001] The invention relates to a preparation method of a fluorination catalyst, in particular to a preparation method of a catalyst used for the gas-phase fluorination reaction of halogenated hydrocarbons and hydrogen fluoride, especially a preparation method of a gas-phase fluorination catalyst used to catalyze the preparation of R134a. Background technique [0002] In recent years, studies have found that hydrofluorocarbons ((HFCs) have an ozone depletion potential (ODP) of 0 and a low global warming potential (GWP), and are widely used in large commercial refrigerants, blowing agents, fire extinguishing agents, etc. At present, the key production process of mainstream environmentally friendly refrigerants (R125, R134a, R1234yf) products in the market is the gas-phase fluorination catalytic reaction process. The fluorination catalyst mainly adopts chromium-based solid catalyst or aluminum-based solid catalyst; a large number of studies have found that the ...

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): B01J23/26B01J35/10B01J37/00B01J37/03B01J37/26C07C17/20C07C19/08
CPCC07C17/206B01J23/26B01J37/0018B01J37/038B01J37/26B01J35/60B01J35/615C07C19/08
Inventor 李义涛黄永锋胡聿明余航梁任龙
Owner RUYUAN DONGYANG LIGHT FLUORIDE CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com