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Method for cracking hexafluoropropylene dipolymer to prepare perfluoro amyl ether and perfluoro amyl ether

A technology of hexafluoropropylene dimer and perfluoroamyl ether, which is applied in the field of perfluoroamyl ether, can solve the problems of less application, more by-products, large power consumption, etc., and achieves simple process operation and high conversion efficiency , the effect of less by-products

Inactive Publication Date: 2019-03-22
TIANJIN CHANGLU CHEM NEW MATERIAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Methods (2) and (3) are rarely used in actual production due to the high cost of the preparation process and low product yield
Most reports are method (4) using the addition reaction of fluorine-containing alcohols and fluorine-containing olefins to prepare hydrofluoroethers. The produced hydrofluoroethers are either flammable or have a pungent odor, which does not meet the needs of the electronics and other industries. ; and in the process of preparing hydrofluoroethers by the reaction of fluorine-containing alcohols and fluorinated olefins, there will be the production of double bond by-products close to the boiling point of the target product, so the purification process of the final product is increased, and all chlorine or bromine in the purification process High toxicity, strict operation requirements
In method (5), the method of electrofluorination chemistry is usually used to prepare fluorinated acid fluorides, and further to prepare hydrofluoroethers. However, the electrofluorination chemistry method not only consumes a lot of electricity, has low yield and many by-products in the production process, but also The process requires a large amount of anhydrous hydrogen fluoride; and electrofluorine chemistry usually produces a large number of isomers rather than a specific perfluorinated acid fluoride, which are almost impossible to use due to the same or similar boiling points. Separation and purification by rectification technology, the resulting hydrofluoroether product is also a mixture, which cannot be separated by rectification technology

Method used

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  • Method for cracking hexafluoropropylene dipolymer to prepare perfluoro amyl ether and perfluoro amyl ether
  • Method for cracking hexafluoropropylene dipolymer to prepare perfluoro amyl ether and perfluoro amyl ether
  • Method for cracking hexafluoropropylene dipolymer to prepare perfluoro amyl ether and perfluoro amyl ether

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Embodiment 1

[0036] Embodiment 1: Preparation of hexafluoropropylene dimer raw material: Hexafluoropropylene gas is passed through the catalytic reaction tube equipped with NaF / Al2O3 catalyst, the loading capacity of the catalyst is 10%, and the contact time is 0.1s; the temperature of the catalytic reaction tube The temperature is 150°C. The reacted mixed gas enters the condenser with a cooling jacket from the gas port inlet. The temperature of the condensed water is 10°C. The unreacted hexafluoropropylene is circulated to the catalytic reaction tube through the gas outlet. The purity of the liquid hexafluoropropylene dimer in the receiver of the condenser was detected to be 99.3%. The yield of hexafluoropropylene dimer is shown in Table 1.

Embodiment 2

[0037] Example 2: Preparation of raw materials for hexafluoropropylene dimer: Hexafluoropropylene gas is passed through a catalytic reaction tube equipped with an AgF / C catalyst, the loading capacity of the catalyst is 15%, the temperature of the catalyst packed column is 180°C, and the contact time is For 10s, the reacted mixed gas enters the condenser with a cooling jacket through the air inlet, and the temperature of the condensed water is 10°C; the unreacted hexafluoropropylene is circulated to the catalytic reaction column through the outlet. The purity of the liquid hexafluoropropylene dimer in the condenser was detected to be 99.2%. The productive rate of hexafluoropropylene dimer after applying mechanically is shown in Table 1.

Embodiment 3

[0038] Embodiment 3: the preparation of hexafluoropropylene dimer raw material: hexafluoropropylene gas is passed through the catalytic reaction tube that KF / C catalyst is housed, and the loading capacity of catalyst is 20%, and the temperature of catalyst packing column is 220 ℃, contact time The reaction time is 30s; the reacted mixed gas enters the condenser with a cooling jacket through the air inlet, the temperature of the condensed water is 10°C, and the unreacted hexafluoropropylene is circulated to the catalytic reaction tube through the outlet. The purity of the liquid hexafluoropropylene dimer in the condenser was detected to be 99.3%. The productive rate of hexafluoropropylene dimer after applying mechanically is shown in Table 1.

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Abstract

The invention belongs to the field of fluorine chemical industry and specifically relates to a method for cracking hexafluoropropylene dipolymer to prepare perfluoro amyl ether and perfluoro amyl ether. The preparation method comprises the steps: 1) perfluoro pentacarbonyl ketone preparation: 1.1) sending the hexafluoropropylene dipolymer into an oxidizing furnace to perform cracking reaction withoxygen under the first catalyst condition; separating a cracked product to obtain perfluoro acetylfluoride; 1.2) preparing the perfluoro pentacarbonyl ketone under the second catalyst action with hexafluoropropylene and the perfluoro acetylfluoride prepared in the step 1.1) as raw materials; 2) selectively adding tertiary amine or a phase transfer catalyst into an inert dipole non-proton organiccompound solution to react under the alkali metal fluoride action with the pentacarbonyl ketone obtained in the step 1) and an alkylation reagent as the raw materials, so as to prepare the perfluoro amyl ether. According to the method disclosed by the invention, hexafluoropropylene tripolymer is utilized as a raw material to generate the perfluoro pentacarbonyl ketone, and then the perfluoro pentacarbonyl ketone reacts with the alkylation reagent to generate the perfluoro amyl ether; thus, the conversion efficiency is high, conditions are moderate, and the whole technological process is simpleto operate.

Description

technical field [0001] The invention belongs to the field of fluorine chemical industry, and in particular relates to a method for preparing perfluoroamyl ether by cracking hexafluoropropylene dimer and perfluoroamyl ether. Background technique [0002] Hydrofluoroethers (HFEs) are a class of commercially valuable compounds. Hydrofluoroethers have found use as replacements for chlorofluorocarbons (CFCs) in numerous applications. Unlike chlorofluorocarbons, hydrofluoroethers containing fluorine as the only halogen basically do not affect the Earth's ozone layer. The Ozone Depletion Potential (ODP) exhibited by such hydrofluoroethers (HFEs) is therefore considered to be zero. In addition, this hydrofluoroether is more easily degraded in the earth's atmosphere, and its low global warming potential (GWP) and short atmospheric residence time make it an ideal replacement for chlorofluorocarbons (CFCs). [0003] Hydrofluoroethers generally refer to those ethers in which hydrogen...

Claims

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Application Information

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IPC IPC(8): C07C51/58C07C53/48C07C45/45C07C49/167C07C41/01C07C43/12
CPCC07C41/01C07C43/12C07C45/455C07C51/58C07C53/48C07C49/167
Inventor 姚素梅贺光瑞郭海强李希仑
Owner TIANJIN CHANGLU CHEM NEW MATERIAL CO LTD
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