IP Library Granted Patent US 11,739,208
Granted Patent B2
US 11,739,208 · App. 17/444,969 · Granted Aug 29, 2023

Block copolymers and uses thereof

Inventors: Xavier D. D. J. Muyldermans (Mont-Saint-Guibert, BE); Aparajita Bhattacharya (Houston, TX); Huixian Yang (Houston, TX); Koen van Duin (Amsterdam, NL)
Assignee: KRATON CORPORATION
C08L53/025C08F297/044C08F297/046C08F2810/00C08L2201/02
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Quick Facts
Patent No.
US 11,739,208
App. No.
17/444,969
Granted
Aug 29, 2023
Kind
B2
Abstract

A hydrogenated block copolymer is disclosed comprising a polymer block A and a polymer block B. Prior to hydrogenation, the polymer block A has a first vinyl aromatic compound, and the polymer block B contains monomers a) a styrene compound having a radical reactive group and b) at least one conjugated diene, and optionally (c) a second vinyl aromatic compound that is same or different from the first vinyl aromatic compound. The repeat units of monomer a) forms 10-80 wt. % of the total block copolymer, and 10-70 wt. % of the total weight of block B. After hydrogenation, the polymerized units derived from the monomer b) has a RU of 0-1.5 meq per gram of the hydrogenated block copolymer. The hydrogenated block copolymer exhibits reactivity and higher flow properties before curing, after curing, shows excellent mechanical properties, improved flame resistance, and good solvent resistance.

Claims (48)

1. A hydrogenated block copolymer comprising at least one polymer block A and at least one polymer block B,

wherein prior to hydrogenation,

each block A is a polymer of a first vinyl aromatic compound, and

each block B is a copolymer block of monomer units:

(a) a styrene compound having a radical reactive group,

(b) at least one conjugated diene, and optionally

(c) a second vinyl aromatic compound that is same or different from the first vinyl aromatic compound;

wherein each block A has a peak molecular weight (Mp) of 3 to 60 kg/mol, and each block B has a peak molecular weight (Mp) of 20 to 200 kg/mol; and

wherein the polymerized units derived from the monomer unit (a) constitutes from 10 to 70 wt. % of the total weight of the hydrogenated block copolymer, and from 10 to 80 wt. % of the total weight of the block B;

wherein after hydrogenation,

the polymerized units derived from the monomer (b) has a residual olefinic unsaturation of 0-1.5 meq per gram of the hydrogenated block copolymer; and

wherein the hydrogenated block copolymer has:

i) a DMA 10 rad/s tangent delta peak maximum temperature of −30 to 80° C.,

ii) a gel content, after curing, as measured by a Peroxide Cured Gel Test (PCGT), of >40 wt. % of the total weight of the hydrogenated block copolymer; and

iii) an aromatic blockiness index of 20 to 80%.

2. The hydrogenated block copolymer of claim 1 ,

wherein the monomer unit (a) is para-methylstyrene, the monomer unit (b) is selected from the group consisting of isoprene, butadiene and combinations thereof;

wherein the block B has a Corrected 1,4-diene unit content of 10 to 55%; and

wherein the hydrogenated block copolymer has one or more of:

i) a dielectric permittivity (Dk) at 1 GHz of <2.6,

ii) a dielectric permittivity (Dk) at 10 GHz of <2.6,

iii) a loss tangent (Df) at 1 GHz of <0.002,

iv) a loss tangent (Df) at 10 GHz of <0.002, and

v) a solution viscosity at 25 wt. % in toluene at 25° C. of <2000 cP.

3. The hydrogenated block copolymer of claim 2 , wherein the weight percentage of (a) para-methylstyrene in the B block is between 10 and 50 wt. %.

4. The hydrogenated block copolymer of claim 1 , wherein the block A comprises polymerized para-methylstyrene units.

5. The hydrogenated block copolymer of claim 2 ,

wherein the block B has a Corrected 1,4-diene unit content of up to 50%;

wherein the polymerized units derived from the monomer unit (b) has a residual olefinic unsaturation of 0-0.3 meq per gram of the hydrogenated block copolymer; and

wherein the hydrogenated block copolymer has an aromatic blockiness index of 40% to 75%; and a solution viscosity at 25 wt. % in toluene at 25° C. of <1000 cP.

6. The hydrogenated block copolymer of claim 1 , wherein the hydrogenated block copolymer has a DMA crossover temperature of 100-300° C.

7. The hydrogenated block copolymer of claim 1 , wherein the hydrogenated block copolymer comprises one or more of structures A-B, A-B-A, (A-B-) n , A-B-A-B, (B-A-B-) n X, (B-A-) n X, and (A-B-A-) n X, wherein “X” is a coupling agent residue, and “n” is 1-30.

8. The hydrogenated block copolymer of claim 7 , wherein the coupling agent is selected from the group consisting of methyltrimethoxysilane (MTMS), tetramethoxysilane (TMOS), divinylbenzene (DVB), dimethyladipate (DMA), and combinations thereof.

9. The hydrogenated block copolymer of claim 1 , further comprising a functional group attached to the radical reactive group of the styrene compound of monomer unit (a).

10. A curable composition comprising: 1-99 wt. % of the hydrogenated block copolymer of claim 1 , 0.1-5 wt. %, based on the total weight of the composition, of an initiator selected from a thermal initiator and an actinic initiator.

11. The curable composition of claim 10 , wherein the thermal initiator is a peroxide.

12. The curable composition of claim 10 , further comprising:

one or more co-curing agents selected from 1,2-bis(vinylphenyl)ethylene, butadiene based liquid rubber, divinyl aromatic compound, triallylcyanurate, triallyisocyanurate, vinyl functionalized polyphenylene oxide, bismaleimide aromatic resin, mono or multifunctional acrylate or methacrylate monomers, plasticizers, tackifying resin, styrenic block copolymers comprising one or more polydiene blocks, and combinations thereof;

a flame retardant; and

a solvent selected from the group consisting of aliphatic hydrocarbons, aromatic hydrocarbons, and combinations thereof.

13. The curable composition of claim 10 , further comprising a polyolefin, wherein the curable composition is cured in the melt phase.

14. A blend comprising: 99-1 wt. % of the hydrogenated block copolymer of claim 1 , and 1-99 wt. % of a crystalline polyolefin.

15. The blend of claim 14 , further comprising a flame retardant.

16. The blend of claim 14 , comprising 10-50 wt. % of the hydrogenated block copolymer, 1-20 wt. % of the crystalline polyolefin, and 20-50 wt. % of a flame retardant; wherein the blend has a rating of V0, according to UL94 vertical burn test method.

17. A cured composition obtained by curing the blend of claim 14 .

18. An article comprising the cured composition of claim 17 .

19. A curable composition containing: 100 parts of the hydrogenated block copolymer of claim 1 and 0.5 parts of a peroxide initiator, after curing at 180° C. for 2 hours and after compression molded, has a Dk at 1 GHz of <3.5, and a Df at 1 GHz of <0.003.

20. A curable composition containing 100 parts of the hydrogenated block copolymer of claim 1 and 0.5 parts of a peroxide initiator, after curing at 180° C. for 2 hours and after compression molded, has a Dk at 10 GHz of <2.6, and a Df at 10 GHz of <0.003.

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 Nov 10, 2021
From: MUYLDERMANS, XAVIER D.D.J; BHATTACHARYA, APARAJITA; YANG, HUIXIAN; VAN DUIN, KOEN
To: KRATON POLYMERS LLC
Reel/Frame 058067/0849 →
Continuity (2)
Provisional Application 63065893 · Aug 14, 2020
Related Publication 20220049083A1 · Feb 17, 2022