IP Library Granted Patent US 10,066,098
Granted Patent B2
US 10,066,098 · App. 15/268,166 · Granted Sep 4, 2018

Styrenic block copolymer compositions

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Quick Facts
Patent No.
US 10,066,098
App. No.
15/268,166
Granted
Sep 4, 2018
Kind
B2
Abstract

This disclosure relates to a block copolymer composition comprising a tetra-branched block copolymer (IV) having a true number average molecular weight of 40,000 to 120,000 represented by the general formula (A-B)4X; a tri-branched block copolymer (III) having a true number average molecular weight of from 30,000 to 90,000 represented by the general formula (A-B)3X; di-branched block copolymer (II) having a true number average molecular weight of from 20,000 to 60,000 represented by the general formula (A-B)2X; and a linear diblock copolymer (I) having a true number average molecular weight of from 10,000 to 30,000 represented by the general formula A-B; where A represents a polymer block of a mono alkenyl arene; B represents a polymer block of a conjugated diene, wherein the B has a true number average molecular weight ranging from 7,000 to 20,000 g/mol; and X represents the residue of an alkoxy silane coupling agent.

Claims (29)

1. A block copolymer composition comprising:

a. 0 to 5 weight percent of a tetra-branched block copolymer (IV) having a number average molecular weight of 44,000 to 80,000 represented by the general formula (A-B)4X;

b. greater than 0 to 60 weight percent of a tri-branched block copolymer (III) having a number average molecular weight of from 33,000 to 60,000 represented by the general formula (A-B)3X;

c. 40 to 95 weight percent of a di-branched block copolymer (II) having a number average molecular weight of from 22,000 to 40,000 represented by the general formula (A-B)2X; and

d. 2 to 10 weight percent of a linear diblock copolymer (I) having a number average molecular weight of from 11,000 to 20,000 represented by the general formula A-B; where:

i. A represents a polymer block of a mono alkenyl arene, wherein the A block has a number average molecular weight ranging from 4,000 to 7,000 g/mol;

ii. B represents a polymer block of a conjugated diene, wherein the B block has a number average molecular weight ranging from 7,000 to 13,000 g/mol and a vinyl content of 30 to 50 mol %; and

iii. X represents the residue of an alkoxy silane coupling agent;

wherein the block copolymer composition has a solution viscosity ranging from 100 to 400 centipoise (cP), as measured in 20 wt. % of toluene at 25° C.

2. The composition of claim 1 , wherein the alkoxy silane coupling agent has the formula Rx-Si—(OR′)y, where x is 0 or 1, x+y=4, R and R′ are the same or different, R is selected from the group consisting of aryl hydrocarbon radicals, linear alkyl hydrocarbon radicals and branched alkyl hydrocarbon radicals, and R′ is selected from the group consisting of linear and branched alkyl hydrocarbon radicals.

3. The composition of claim 1 , wherein the block copolymer composition comprises:

a. 0 to 5 wt. %, based upon the total weight of the block copolymer composition, of the tetra-branched block copolymer (IV);

b. greater than 0 to 36 wt. %, based upon the total weight of the block copolymer composition, of the tri-branched block copolymer (III);

c. 60 to 95 wt. %, based upon the total weight of the block copolymer composition, of the di-branched block copolymer (II); and

d. 4 to 8 wt. %, based upon the total weight of the block copolymer composition, of the linear diblock copolymer (I).

4. The composition of claim 1 , wherein the block copolymer composition has a solution viscosity ranging from 140 to 375 centipoise (cP), as measured in 20 wt. % of toluene at 25° C.

5. The composition of claim 1 , wherein the block copolymer composition has a melt flow rate ranging from 20 to 200 g/10 min., as measured at 230° C. with a load of 5 kg.

6. The composition of claim 1 , wherein the block copolymer composition has a tensile strength ranging from 2000 to 8000 psi, as measured on melt cast films.

7. The composition of claim 1 , wherein the block copolymer composition has an anisotropy ratio based upon the MD/CD 300% modulus of less than 1.4.

8. The composition of claim 1 wherein at least one block of the block copolymer composition is functionalized.

9. The composition of claim 8 wherein functionalization comprises grafting with an acid compound or its derivative.

10. The composition of claim 9 wherein said acid compound or its derivative is selected from the group consisting of maleic anhydride, maleic acid, fumaric acid, and its derivatives.

11. The composition of claim 9 wherein said acid compound or its derivative is maleic anhydride or maleic acid.

12. A mixture comprising (i) from about 1 to about 99 weight percent of an engineering thermoplastic resin selected from the group consisting of polyamides, polyesters and copolymer thereof, and polyurethanes and (ii) from about 1 to about 99 weight percent of the composition of claim 11 .

13. The composition of claim 1 further comprising an engineering thermoplastic resin.

14. A mixture comprising (i) from about 5 wt. % to about 95 wt. % of a polyolefin selected from the group consisting of polypropylene, polyethylene, polybutylene, amorphous polyolefin, polyolefin elastomers and copolymers thereof, and (iii) from about 5 wt. % to about 95 wt. % of the composition of claim 1 .

15. A mixture comprising (i) from about 10 wt. % to about 50 wt. % of tackifying resin, (ii) from about 20 wt. % to about 60 wt. % of oil, and (iii) from about 15 wt. % to about 35 wt. % of the composition of claim 1 .

16. A mixture comprising (i) from about 10 wt. % to about 50 wt. % of tackifying resin, and (ii) from about 50 wt. % to about 90 wt. % of the composition of claim 1 .

17. A mixture comprising of a) at least one of (i) from about 0.01 wt. % to about 50 wt. % of a polystyrene polymer or ii) from about 0.01 wt. % to about 30 wt. % of oil, and (b) from about 20 wt. % to about 80 wt. % of the composition of claim 1 .

Assignments (6)
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 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2021
From: FLOOD, JOHN; WRIGHT, KATHRYN J.; MUYLDERMANS, XAVIER D.; WILLIS, CARL L.; GILLEN, JASON; ZHOU, YONGHUA; BROTHERS, AARON
To: KRATON POLYMERS U.S. LLC
Reel/Frame 057239/0558 →
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 →