Sulfonated perfluorocyclobutane ion-conducting membranes

• US 6,559,237 B1
• Filed: 06/05/2000
• Issued: 05/06/2003
• Est. Priority Date: 06/05/2000
• Status: Expired due to Term

• Current Assignee: 3M Innovative Properties Company (3M Company)
• Original Assignee: 3M Innovative Properties Company (3M Company)
• Inventors: Ylitalo, David A., Lewinski, Krzysztof A., Mao, Shane S.
• Primary Examiner(s): Lipman, Bernard
• Application Number:
  US09/587,522
• Time in Patent Office: 1,065 Days
• Field of Search: 525/326.2, 525/344, 525/354, 521/27
• US Class Current: 525/326.2
• CPC Class Codes: C08F 116/14 Monomers containing only one unsaturated aliphatic radical
• CPC Class Codes: C08F 216/125 Monomers containing two or more unsaturated aliphatic radicals, e.g. trimethylolpropane triallyl ether or pentaerythritol triallyl ether
• CPC Class Codes: C08F 216/1408 Monomers containing halogen
• CPC Class Codes: C08F 2800/20 as weight or mass percentages
• CPC Class Codes: C08F 8/36 Sulfonation; Sulfation
• CPC Class Codes: C08J 5/18 Manufacture of films or sheets
• CPC Class Codes: Y02E 60/50 Fuel cells

Abstract

Disclosed are sulfonated aromatic perfluorocyclobutane polymers meeting a condition selected from: a) the equivalent weight of the polymer is 5000 or less, and b) the proton conductivity of the polymer at 25° C. is 0.01 Siemens per centimeter (S/cm) or higher, and methods of making same, especially sulfonated aromatic perfluorocyclobutane polymers which comprise units according to the formula:

wherein —B— is 1,2-perfluorocyclobutylene (C₄F₆); each —X— is independently selected from the group consisting of: a bond, —O—, —S—, —SO—, —SO₂—, —CO—, —NH—, —NR₁—, and —R₂—, wherein R₁ is C1-C25 substituted or unsubstituted, saturated or unsaturated alkyl or aryl and R₂ is C1-C25 substituted or unsubstituted, saturated or unsaturated alkylene or arylene; —Ar— is a substituted or unsubstituted C1-C30 at least divalent aromatic hydrocarbon group; n is a non-negative integer chosen independently for each of said repeating units such that the average for the polymer is greater than 0. They are particularly useful in ion conducting membranes for use in electrochemical cells.

Claims

1. A sulfonated aromatic perfluorocyclobutane polymer meeting a condition selected from:

a) the equivalent weight of the polymer is 5000 or less; and

b) the proton conductivity of the polymer at 25°

C. is 0.01 Siemens per centimeter (S/cm) or higher.

2. The polymer of claim 1 further comprising units according to the formula:

wherein —

B—

is 1,2-perflurorocyclobutylene (C₄F₆);

wherein each —

X—

is independently selected from the group consisting of;

a bond, —

O—

, —

S—

, —

SO—

, —

SO₂—

, —

CO—

, —

NH—

, —

NR₁—

, and —

R₂—

, wherein R₁ is C1-C25 substituted or unsubstituted, saturated or unsaturated alkyl or aryl and R₂ is C1-C25 substituted or unsubstituted, saturated or unsaturated alkylene or arylene;

wherein —

Ar—

is a substituted or unsubstituted C1-C30 at least divalent aromatic hydrocarbon group; and

wherein n is a non-negative integer chosen independently for each of said repeating units such that the average for the polymer is greater than 0.

3. The polymer according to claim 2 wherein the proton conductivity of the polymer at 25°

C. is 0.02 S/cm or higher.

4. The polymer according to claim 2 wherein the proton conductivity of the polymer at 25°

C. is 0.10 S/cm or higher.

5. The polymer according to claim 2 wherein the equivalent weight of the polymer is 1250 or less.

6. The polymer according to claim 2 wherein the equivalent weight of the polymer is 800 or less.

7. The polymer according to claim 2 wherein —

X—

is —

O—

.

8. The polymer according to claim 2 wherein —

Ar—

is 4,4′

-biphenylene.

9. An ion conducting membrane comprising the polymer according to claim 2.

10. The polymer according to claim 2 having at least one property selected from:

a) a dry break strength of 15 MPa or greater; and

b) a wet break strength of 10 MPa or greater.

11. A polymer according to claim 2 which is branched and which additionally comprises units according to the formula:

wherein —

B—

, —

X— and

n are defined as above; and

wherein —

Ar—

is a substituted or unsubstituted C1-C30 at least trivalent aromatic hydrocarbon group.

12. The polymer according to claim 11 wherein —

Ar—

is 1,1,1-tris(4-phenylene) ethane.

13. The polymer according to claim 12 wherein —

X—

is —

O—

.

14. A polymer blend comprising the polymer according to claim 2 wherein said blend has a proton conductivity at 25°

C. of 0.02 S/cm or higher.

15. A polymer blend according to claim 14 additionally comprising a fluoropolymer.

16. An ion conducting membrane comprising the polymer blend according to claim 15.

17. A process for preparing a polymer comprising the step of sulfonating a perfluorocyclobutane polymer to form a sulfonated perfluorocyclobutane polymer, wherein said sulfonated perfluorocyclobutane polymer is sufficiently sulfonated as to meet a condition selected from:

a) the equivalent weight of the polymer is 5000 or less; and

b) the proton conductivity of the polymer at 25°

C. is 0.01 S/cm or higher.

18. The process according to claim 17, wherein the sulfonated perfluorocyclobutane polymer has a structure comprising units according to the formula:

wherein —

B—

is 1,2-perflurorocyclobutylene (C₄F₆);

wherein each —

X—

is independently selected from the group consisting of;

a bond, —

O—

, —

S—

, —

SO—

, —

SO₂—

, —

CO—

, —

NH—

, —

NR₁—

, and —

R₂—

, wherein R₁ is C1-C25 substituted or unsubstituted, saturated or unsaturated alkyl or aryl and R₂ is C1-C25 substituted or unsubstituted, saturated or unsaturated alkylene or arylene;

wherein —

Ar—

is a substituted or unsubstituted C1-C30 at least divalent aromatic hydrocarbon group; and

wherein n is a non-negative integer chosen independently for each of said repeating units such that the average for the polymer is greater than zero.

19. The process according to claim 17, wherein the step of sulfonation is accomplished by

A) applying a halosulfonic acid to add sulfonyl halide groups to the perfluorocyclobutane polymer;

and thereafter

B) hydrolyzing said sulfonyl halide groups to form sulfonic acid groups.

20. A process for preparing a proton exchange membrane comprising the step of claim 19, additionally comprising the steps of forming the polymer into a membrane after A) and before B).

21. The process according to claim 17, wherein the step of sulfonation is accomplished by application of sulfuric acid.

22. The process according to claim 17, wherein the step of sulfonation provides a polymer having at least one property selected from:

a) a dry break strength of 15 MPa or greater; and

b) a wet break strength of 10 MPa or greater.

23. The process of to claim 17, wherein the polymer is in the form of a membrane.

24. A process for preparing a sulfonated perfluorocyclobutane polymer comprising:

A) providing a perfluorocyclobutane polymer including sulfur-containing groups; and

B) converting said sulfur-containing group into a sulfonic acid group to form a sulfonated perfluorocyclobutane polymer, wherein said sulfonated perfluorocyclobutane polymer is sufficiently sulfonated as to meet a condition selected from;

a) the equivalent weight of the polymer is 5000 or less; and

b) the proton conductivity of the polymer at 25°

C. is 0.01 S/cm or higher.

25. The process according to claim 24, wherein the step of converting is accomplished by hydrolysis.

26. The process according to claim 24, wherein said sulfur-containing groups are sulfonyl halide groups.

27. A process for preparing a proton exchange membrane comprising the steps of claim 24, additionally comprising the step of forming said polymer into a membrane after A) and before B).