IP Library Granted Patent US 8,329,827
Granted Patent B2
US 8,329,827 · App. 12/763,979 · Granted Dec 11, 2012

Sulfonated block copolymers having ethylene and diene interior blocks, and various uses for such block copolymers

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Quick Facts
Patent No.
US 8,329,827
App. No.
12/763,979
Granted
Dec 11, 2012
Kind
B2
Abstract

A sulfonated block copolymer which is solid and non-dispersible in water having at least two polymer end blocks A and at least one interior block B wherein each A block is a polymer block resistant to sulfonation and each B block is a polymer block susceptible to sulfonation, wherein the A and B blocks do not contain any significant levels of olefinic unsaturation. Each A block includes one or more segments selected from polymerized (i) ethylene, (ii) monomers of conjugated dienes having a vinyl content less than 35 mol percent prior to hydrogenation, and (iii) mixtures thereof; and each B block comprising segments of one or more polymerized vinyl aromatic monomers selected from (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof.

Claims (24)

1. A sulfonated block copolymer which is solid in water comprising at least two polymer end blocks A, at least one polymer interior block B wherein:

a. each A block is a polymer block resistant to sulfonation and each B block is a polymer block susceptible to sulfonation, said A and B blocks containing no significant levels of olefinic unsaturation;

b. each A block independently having a number average molecular weight between 1,000 and 60,000 and each B block independently having a number average molecular weight between 10,000 and 300,000;

c. each A block comprising one or more segments selected from polymerized (i) ethylene, (ii) monomers of conjugated dienes having a vinyl content less than 20 mol percent prior to hydrogenation, and (iii) mixtures thereof, wherein any segments containing polymerized conjugated dienes are subsequently hydrogenated and have a crystalline or semi-crystalline structure subsequent hydrogenation and wherein any A block comprising polymerized ethylene or hydrogenated polymers of a conjugated, acyclic diene have a melting point greater than 50° C.;

d. each B block comprising segments of one or more vinyl aromatic monomers selected from polymerized (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof;

e. said B blocks are sulfonated to the extent of 10 to 100 mol percent, based on the units of vinyl aromatic monomer in said B blocks; and

f. the mol percent of vinyl aromatic monomers which are unsubstituted styrene monomers, ortho-substituted styrene monomers, meta-substituted styrene monomers, alpha-methylstyrene, 1,1-diphenylethylene and 1,2-diphenylethylene in each B block being between 10 mol percent and 100 mol percent; and

g. said sulfonated block copolymer is non-dispersible and solid in water, and has a tensile strength greater than 100 psi in the presence of water according to ASTM D412 after immersion in water for 24 hours.

2. The sulfonated block copolymer according to claim 1 , wherein said A block is a segment of polymerized ethylene having a number average molecular weight between 1,000 and 60,000.

3. The sulfonated block copolymer according to claim 1 , wherein said A block prior to hydrogenation is a polymerized segment of a low vinyl content 1,3-butadiene, and wherein said vinyl content prior to hydrogenation is less than 20 mol percent.

4. The sulfonated block copolymer according to claim 1 , wherein said A block comprises up to 15 mol percent of polymerized monomers selected from (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof.

5. The sulfonated block copolymer according to claim 1 , wherein the interior block B is a hydrogenated copolymer of one or more unsubstituted styrene monomers, and monomers of conjugated dienes having a vinyl content of 20 to 80 mol percent prior to hydrogenation.

6. The sulfonated block copolymer according to claim 1 , wherein said B block is a random copolymer, a tapered copolymer or a controlled distribution copolymer.

7. The sulfonated block copolymer according to claim 1 , further comprising at least one polymer block D having a glass transition temperature of less than 20° C. and a number average molecular weight of between 1,000 and 50,000.

8. The sulfonated block copolymer according to claim 7 , wherein said D block prior to hydrogenation is polymer block of 1,3-butadiene, and wherein 20 to 80 mol percent of the condensed butadiene units in block D have 1,2-configuration prior to hydrogenation.

9. The sulfonated block copolymer according to claim 1 , having the general configuration A-D-B-D-A, A-B-D-B-A, (A-D-B) n X, (A-B-D) n X, A-B-A, A-B-A-B-A, (A-B-A) n X, or (A-B) n X, or mixtures thereof, where n is an integer from 2 to about 30, and X is coupling agent residue.

10. The sulfonated block copolymer according to claim 9 , wherein said D block being selected from the group consisting of (i) a polymerized or copolymerized conjugated diene selected from isoprene and 1,3-butadiene having a vinyl content prior to hydrogenation of between 20 and 80 mol percent, (ii) a polymerized acrylate monomer, (iii) a silicon polymer, (iv) polymerized isobutylene and (v) mixtures thereof, wherein any segments containing polymerized 1,3-butadiene or isoprene are subsequently hydrogenated.

11. The sulfonated block copolymer according to claim 1 , having a water permeability greater than 0.1 times 10 −6 grams per Pascal.meter.hour, according to ASTM E96-00 “desiccant” method, a wet tensile strength greater than 500 psi according to ASTM D412, and a swellability of less than 100% weight after immersion in water for 24 hours.

12. The sulfonated block copolymer according to claim 1 , having a water permeability greater than 1.0 times 10 −6 grams per Pascal.meter.hour, according to ASTM E96-00 “desiccant” method and a wet tensile strength greater than 1000 psi according to ASTM D412 after immersion in water for 24 hours.

13. The sulfonated block copolymer according to claim 1 , having a ratio of wet tensile strength to dry tensile strength greater than 0.3.

14. An article formed at least in part from a composition comprising the sulfonated block copolymer of claim 1 , said article being selected from the group consisting of fuel cells, fabrics, coated fabrics, membranes, filtration membranes, desalination membranes, air conditioning membranes, heat recovery membranes, coatings for membranes, personal hygiene articles, adhesives, hydrogels, antifouling coatings, water absorption articles, electrode assemblies, and marine coatings.

15. The sulfonated block copolymer according to claim 1 , wherein each A block comprises one or more segments selected from polymerized monomers of conjugated dienes having a vinyl content of less than 15 mol percent prior to hydrogenation.

16. The sulfonated block copolymer according to claim 1 , wherein any A block comprising polymerized ethylene or hydrogenated polymers of a conjugated, acyclic diene have a melting point greater than 80° C.

17. The sulfonated block copolymer according to claim 1 , wherein each end block A is other than solely hydrogenated polymer segments of conjugated dienes.

Assignments (7)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jul 24, 2024
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: KRATON CHEMICAL, LLC; KRATON CORPORATION
Reel/Frame 068671/0836 →
CORRECTIVE ASSIGNMENT TO CORRECT THE PATENT NO. 8837224 TO PATENT NO. 7737224 PREVIOUSLY RECORDED AT REEL: 037448 FRAME: 0453. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 11, 2022
From: KRATON POLYMERS U.S. LLC; ARIZONA CHEMICAL COMPANY, LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 060344/0919 →
SECURITY INTEREST Recorded Mar 18, 2022
From: KRATON CHEMICAL, LLC; KRATON POLYMERS LLC; KRATON POLYMERS U.S. LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 059525/0804 →
SECURITY INTEREST Recorded Mar 18, 2022
From: KRATON CHEMICAL, LLC; KRATON POLYMERS LLC; KRATON POLYMERS U.S. LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 059864/0455 →
RELEASE OF SECURITY INTEREST Recorded Mar 16, 2022
From: BANK OF AMERICA, N.A.
To: KRATON POLYMERS U.S. LLC; KRATON CHEMICAL, LLC F/K/A ARIZONA CHEMICAL COMPANY, LLC; KRATON POLYMERS LLC; KRATON CORPORATION; KRATON CHEMICAL B.V.
Reel/Frame 059910/0017 →
RELEASE OF SECURITY INTEREST Recorded Mar 15, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: KRATON POLYMERS U.S. LLC
Reel/Frame 059366/0611 →
SECURITY INTEREST Recorded Apr 16, 2020
From: KRATON POLYMERS U.S. LLC; KRATON CHEMICAL, LLC F/K/A ARIZONA CHEMICAL COMPANY, LLC; KRATON POLYMERS LLC; KRATON CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 053020/0101 →