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(PER)fluoropolyether polymers

A technology of polymers and polyethers, which can be used in lubricating compositions, instruments, recording information storage, etc., and can solve problems such as attacks

Pending Publication Date: 2019-07-30
SOLVAY SOLEXIS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, a random distribution of repeating units can result in a sequence comprising multiple consecutive repeating units with one carbon atom (i.e., having the formula -CF 2 O-), which on the one hand increases the flexibility of the polymer backbone, but on the other hand constitutes a weak point in the polymer backbone, since they are more easily attacked by metals and / or Lewis acids

Method used

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  • (PER)fluoropolyether polymers

Examples

Experimental program
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Effect test

example 1

[0190] Step (a): Synthesis of HO(CH 2 ) 4 OCF 2 CFHO(CF 2 ) 4 OCFHCF 2 O(CH 2 ) 4 OH

[0191] A three-necked round bottom flask with magnetic stirring, temperature probe and reflux condenser was charged with 5.76 g of NaOH and 227.76 g of 1,4-butanediol. The mixture was heated at 70°C with stirring until the sodium hydroxide was completely dissolved. Then, the solution was cooled to 40°C, and 50 g of CF was added dropwise 2 =CFO(CF 2 ) 4 OCF=CF 2 . The resulting mixture was kept at 40°C for six hours under stirring until the perfluorobisvinyl ether was completely converted. Use 80ml of water and 80ml of CH for the crude product 2 Cl 2 Extraction; 120ml of fresh CH is used again 2 Cl 2 The aqueous phase was extracted, and the two organic phases were collected and extracted with brine (80 ml). Separate the organic phase and use anhydrous Na 2 SO 4 Work up, filter, and evaporate the solvent under reduced pressure to obtain 57.7 g of a mixture containing:

[0192] HO(CH 2 ) 4 [OCF 2...

example 2

[0204] Step (a): Synthesis of HO(CH 2 ) 3 [OCF 2 CFHO(CF 2 ) 3 OCFHCF 2 O(CH 2 ) 3 ] n OH

[0205] A three-neck round bottom flask with magnetic stirring, temperature probe and reflux condenser was charged with 6.69 g of NaOH, 82.40 g of 1,3-propanediol and 200 ml of acetonitrile. The mixture was heated at 40°C with stirring until the sodium hydroxide was completely dissolved. Then, add 107.40g of CF dropwise 2 =CFO(CF 2 ) 3 OCF=CF 2 . The resulting mixture was kept at 40°C for six hours with stirring until the perfluorobisvinyl ether was completely converted. Use 200ml of water and 200ml of CH for the crude product 2 Cl 2 Extraction; again with 200ml of fresh CH 2 Cl 2 The aqueous phase was extracted, and the two organic phases were collected and extracted with brine (200 ml). Separate the organic phase and use anhydrous Na 2 SO 4 Work up, filter, and evaporate the solvent under reduced pressure to obtain a mixture containing:

[0206] 33% of those who have the formula HO(CH 2 ...

example 3

[0215] Step (a): Synthesis of [HO(CH 2 ) 4 OCF 2 CFHOCF 2 OCF 2 CF 2 ] 2 O

[0216] A three-necked round bottom flask with magnetic stirring, temperature probe and reflux condenser was filled with 3.95g of NaOH, 178g of 1,4-butanediol and 80ml of HCF 2 CF 2 OCH 2 CH 2 OCF 2 CF 2 H. The mixture was heated at 70°C with stirring until the sodium hydroxide was completely dissolved, and then 54 g of [CF 2 =CFOCF 2 OCF 2 CF 2 ] 2 O. The resulting mixture was kept at 70°C for three hours under stirring until the perfluorobisvinyl ether was completely converted. The crude product was extracted with 150 ml of water; the organic layer was separated and the solvent was evaporated under reduced pressure at 100°C. The remaining viscous oil was filtered to obtain 33 g of a mixture containing: HO(CH 2 ) 4 [OCF 2 CFHOCF 2 O(CF 2 ) 2 O(CF 2 ) 2 OCF 2 OCFHCF 2 O(CH 2 ) 4 ] n OH, where n is from 1 to 4.

[0217] Step (b): Synthesis (EtOC(O)CF 2 CF 2 CF 2 OCF 2 CF 2 OCF 2 OCF 2 CF 2 -) 2 O and highe...

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Abstract

The present invention relates to a novel process for the synthesis of (per)fluoropolyether polymers, to certain novel (per)fluoropolyether polymers. The present invention also relates to the use of the (per)fluoropolyether polymers thus obtained as intermediate compounds for the manufacture of further polymers suitable for use as lubricants, notably for magnetic recording media (MRM).

Description

[0001] Cross reference to related patent applications [0002] This application claims the priority of European patent application number 16204181.8 filed on December 14, 2016, and the entire content of the application is incorporated into this application by reference for all purposes. Technical field [0003] The present invention relates to a new process for synthesizing (per)fluoropolyether polymers, and relates to some new (per)fluoropolyether polymers. The present invention also relates to the use of the (per)fluoropolyether polymers thus obtained as intermediate compounds for the manufacture of additional polymers suitable for use notably in magnetic recording media (MRM) Lubricant. Background technique [0004] Among fluorinated polymers, (per)fluoropolyether polymers (PFPE) are well known and have received a lot of attention due to their chemical and physical properties, which makes them particularly attractive as lubricants. [0005] The synthesis of several PFPE polymers ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08G65/00C08G65/323C08G65/324C08G65/331
CPCC08G65/007C08G65/3236C08G65/324C08G65/3312G11B5/71C10M107/38
Inventor C.蒙扎尼V.托尔泰利M.加里伯蒂R.瓦尔瑟奇P.马可尼
Owner SOLVAY SOLEXIS