IP Library Granted Patent US 11,279,821
Granted Patent B2
US 11,279,821 · App. 16/946,546 · Granted Mar 22, 2022

Ultrahigh melt flow styrenic block copolymers

Inventors: John E Flood (Houston, TX); Xavier Muyldermans (Mont St. Guibert, BE)
Assignee: Kraton Polymers LLC
C08L53/025C08L51/006C09J123/02C09J153/025
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Quick Facts
Patent No.
US 11,279,821
App. No.
16/946,546
Granted
Mar 22, 2022
Kind
B2
Abstract

A selectively hydrogenated block copolymer of general formula S-E-S, (S-E 1 ) n X, or mixtures thereof is disclosed, where n has a value of 2-6, and X is a coupling agent residue. Before hydrogenation, S is a polystyrene block having a molecular weight of 4,400-5,600 g/mol, and E and E1 are polydiene blocks having molecular weights of 18,000-36,000 g/mol and 9,000 to 18,000 g/mol, respectively, selected from polybutadiene, polyisoprene and mixtures thereof, and having a total vinyl content of 60-85 mol %. After hydrogenation, the block copolymer has 0-10 percent of styrene double bonds reduced and at least 80 percent of conjugated diene double bonds reduced. The block copolymer has a solution viscosity of less than 80 centipoise (cP); a polystyrene content of 25-40 wt. % and up to 50 wt. % of diblock units of general formula S-E or S-E 1 .

Claims (61)

1. A selectively hydrogenated block copolymer having an S block and an E or E 1 block and having a general formula: S-E-S, (S-E 1 ) n X, or mixtures thereof,

wherein:

n has a value of 2 to 6;

X is a coupling agent residue;

the S block has a molecular weight of 4,400 to 5,600 g/mol;

the block copolymer has a solution viscosity at 25 wt. % toluene and 25° C. of less than 70 centipoise (cP);

the block copolymer has a polystyrene content of 25 to 40 wt. %; and

up to 50 wt. % of diblock units in the block copolymer have a general formula S-E or S-E 1 ;

wherein prior to hydrogenation:

the S block is a polystyrene block;

the E block is a polydiene block selected from the group consisting of polybutadiene, polyisoprene and mixtures thereof, and having a molecular weight of from 18,000 to 36,000 g/mol;

the E 1 block is a polydiene block selected from the group consisting of polybutadiene, polyisoprene and mixtures thereof, and having a molecular weight of from 9,000 to 18,000 g/mol;

the polydiene block has a total vinyl content of 60 to 85%; and

wherein subsequent to hydrogenation:

0-10 percent of styrene double bonds in the block copolymer are reduced,

at least 80 percent of conjugated diene double bonds in the block copolymer are reduced; and

wherein

the block copolymer has a melt index from 80 to 1300 g/10 min. at 190° C. and 2.16 kg weight, according to ASTM D1238;

the block copolymer has an elongation at break of at least 300%, as measured on compression molded films according to ASTM D412; and

the block copolymer has a tensile strength of at least 1.5 MPa, as measured on compression molded films according to ASTM D412.

2. The block copolymer of claim 1 , wherein the block copolymer has an order-disorder temperature (ODT) of less than 230° C.

3. The block copolymer of claim 1 , wherein the block copolymer has a formula S-E-S, with less than 10 wt. % of a diblock copolymer of formula S-E.

4. The block copolymer of claim 1 , wherein the block copolymer has a formula (S-E 1 ) n X, with between 5 and 50 wt. % of a diblock copolymer of formula S-E 1 .

5. The block copolymer of claim 1 , wherein the coupling agent is selected from the group of methyl benzoate, silicon tetrachloride, alkoxy silanes, polyepoxides, polyisocyanates, polyimines, polyaldehydes, polyketones, polyanhydrides, polyesters, polyhalides, diesters, methoxy silanes, divinyl benzene, 1,3,5-benzenetricarboxylic acid trichloride, glycidoxytrimethoxy silanes, oxydipropylbis(trimethoxy silane), and mixtures thereof.

6. The block copolymer of claim 1 , wherein the block copolymer has a formula of S-E-S, and a solution viscosity ranging from 10 cP to 70 cP, measured as a 25 wt. % solution in toluene at 25° C.

7. The block copolymer of claim 1 , wherein the block copolymer has a formula of (S-E 1 ) n X, and a solution viscosity ranging from 10 to 50 cP, measured as a 25 wt. % solution in toluene at 25° C.

8. The block copolymer of claim 1 wherein the block copolymer is functionalized with a functional group selected from fumaric acid, itaconic acid, citraconic acid, acrylic acid, maleic anhydride, itaconic anhydride, citraconic anhydride, and their derivatives and derivatives thereof.

9. The block copolymer of claim 8 , wherein the block copolymer is functionalized by grafting maleic anhydride onto the block copolymer.

10. An adhesive composition comprising:

0 to about 80 wt. % of a poly-alpha-olefin

10 to about 60 wt. % of a tackifying resin, and

10 to about 50 wt. % of the hydrogenated block copolymer of claim 1 .

11. A composition comprising:

the selectively hydrogenated block copolymer of claim 1 ;

0.001 to 90 wt. % of an additive selected from olefin polymers, thermoplastic polyurethane, thermoplastic copolyester, styrene polymers, thermoplastic elastomers, tackifying resins, polymer extending oil, waxes, fillers, lubricants, stabilizers, engineering thermoplastic resins, and mixtures thereof.

12. The composition of claim 11 , wherein the additive is a high flow polyolefin having a melt flow rate of >40 g/10 min.

13. The composition of claim 11 , wherein the selectively hydrogenated block copolymer has an order-disorder temperature (ODT) of 140-230° C.

14. An article comprising the composition of claim 11 , wherein the article is selected from the group of toys, medical devices, films, tubing, profiles, 3D printed article, sheet, coating, band, strip, molding, tube, foam, tape, fabric, thread, filament, ribbon, fibers, fibrous web, overmolded automotive parts, dipped goods, sheet molded articles, hot melt adhesives, tie-layers, roofing sheets, membranes, tire treads, and tire inner layers.

15. The article of claim 14 , wherein the article is formed by injection molding, overmolding, dipping, extrusion, roto-molding, slush molding, fiber spinning, film making, 3D printing or foaming.

16. A composition comprising:

a selectively hydrogenated block copolymer having an S block and an E or E 1 block and having the general formula S-E-S, (S-E 1 ) n X or mixtures thereof,

wherein:

n has a value of 2 to 6,

X is a coupling agent residue,

the block copolymer has a styrene content of 29 to 37 wt. %, the block copolymer has a solution viscosity at 25 wt. % solution in toluene at 25° C. of 10 to 70 centipoise (cP);

wherein prior to hydrogenation

the S block is a polystyrene block,

the E block is a polydiene block, selected from the group consisting of polybutadiene, polyisoprene and mixtures thereof, having a molecular weight of from 18,000 to 36,000 g/mol,

the E 1 block is a polydiene block, selected from the group consisting of polybutadiene, polyisoprene and mixtures thereof, having a molecular weight of from 9,000 to 18,000 g/mol,

the polydiene blocks have a total vinyl content of 70 to 85%;

wherein subsequent to hydrogenation

0-10 percent of the styrene double bonds have been hydrogenated; and

at least 80 percent of conjugated diene double bonds in the block copolymer are reduced; and

wherein the block copolymer is functionalized with 0.1 to 10 wt. % of a monomer

selected from fumaric acid, itaconic acid, citraconic acid, acrylic acid, maleic

anhydride, itaconic anhydride, citraconic anhydride, and derivatives thereof; and

wherein

the block copolymer has a melt index from 80 to 1300 g/10 min. at 190° C. and 2.16 kg weight, according to ASTM D1238;

the block copolymer has an elongation at break of at least 300%, as measured on compression molded films according to ASTM D412; and

the block copolymer has a tensile strength of at least 1.5 Mpa, as measured on compression molded films according to ASTM D412.

17. The composition of claim 16 , wherein the selectively hydrogenated block copolymer has an order-disorder temperature (ODT) of less than 230° C.

Assignments (4)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2021
From: FLOOD, JOHN E.; MUYLDERMANS, XAVIER
To: KRATON POLYMERS LLC
Reel/Frame 058486/0291 →
Continuity (3)
Continuation In Part 16360094 · Mar 21, 2019
Provisional Application 62647218 · Mar 23, 2018
Related Publication 20200325324A1 · Oct 15, 2020