IP Library Granted Patent US 6,916,955
Granted Patent B2
US 6,916,955 · App. 10/632,723 · Granted Jul 12, 2005

Process for synthesizing perfluorinated polyethers with metal carboxylate end groups

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Quick Facts
Patent No.
US 6,916,955
App. No.
10/632,723
Granted
Jul 12, 2005
Kind
B2
Abstract

A process is provided for synthesizing metal salts of perfluorinated polyethers containing at least one carboxylic acid group. The polymeric salts so provided are effective as anti-wetting and corrosion-protective agents. The metal salts of perfluorinated polyether acids may be used to prepare corrosion-protected substrates, including magnetic recording disks and magnetic recording heads.

Claims (20)

1. A process for preparing a metal salt of a perfluorinated polyether having at least one carboxylic acid end group, comprising:

treating a fluorinated polyether having at least one carboxylic acid end group with a metal salt of a volatile organic acid under reaction conditions effective to convert all carboxylic acid end groups to the salt form and volatilize the resulting organic acid, thus providing a reaction product comprising a salt of the metal and the fluorinated polyether.

2. The process of claim 1 , wherein the fluorinated polyether is a perfluorinated polyether.

3. The process of claim 2 , wherein the perfluorinated polyether is comprised of monomer units having the structure —CF 2 —O—, —CF 2 —CF 2 —O—, —CF(CF 3 )—O—, —CF(CF 3 )—CF 2 —O—, or a combination thereof.

4. The process of claim 3 , wherein the perfluorinated polyether is a linear polymer.

5. The process of claim 4 , wherein the perfluorinated polyether has a single carboxylic acid end group.

6. The process of claim 4 , wherein the perfluorinated polyether has two carboxylic acid end groups.

7. The process of claim 2 , wherein the metal salt is an alkali metal salt.

8. The process of claim 7 , wherein the alkali metal salt is a sodium salt.

9. The process of claim 2 , wherein the volatile organic acid is acetic acid.

10. The process of claim 7 , wherein the volatile organic acid is acetic acid.

11. The process of claim 8 , wherein the volatile organic acid is acetic acid.

12. The process of claim 2 , wherein the reaction conditions comprise heating a mixture of the fluorinated polyether and the metal salt of a volatile organic acid at a temperature of at least about 130° C. for at least 48 hours.

13. The process of claim 2 , further comprising isolating the reaction product.

14. The process of claim 13 , wherein the product is isolated by an extraction process.

15. The process of claim 14 , wherein the extraction process employs a fluorinated alkane solvent and a lower alkanol.

16. The process of claim 15 , wherein the extraction process employs perfluorohexane and methanol.

17. The process of claim 2 , wherein the perfluorinated polyether has a number average molecular weight in the range of approximately 500 to 10,000.

18. The process of claim 17 , wherein the perfluorinated polyether has a number average molecular weight in the range of approximately 1000 to 5,000.

19. The process of claim 18 , wherein the perfluorinated polyether has a number average molecular weight in the range of approximately 2500 to 3500.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2016
From: HGST NETHERLANDS B.V.
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 040820/0802 →
CHANGE OF NAME Recorded Oct 25, 2012
From: HITACHI GLOBAL STORAGE TECHNOLOGIES NETHERLANDS B.V.
To: HGST NETHERLANDS B.V.
Reel/Frame 029341/0777 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2005
From: INTERNATIONAL BUSINESS MACHINES CORPORATION
To: HITACHI GLOBAL STORAGE TECHNOLOGIES NETHERLANDS B.V.
Reel/Frame 016824/0508 →