IP Library Granted Patent US 11,692,048
Granted Patent B2
US 11,692,048 · App. 16/948,224 · Granted Jul 4, 2023

Fusible oil gel compositions and methods of making and using same

Inventors: Catherine A. L. Maris (Mont S. Guibert, BE); Erin B. Murphy (Houston, TX); Robert C. Bening (Houston, TX); Xiangyun Wei (Houston, TX); Xavier D. Muyldermans (Mont S. Guibert, BE)
Assignee: KRATON CORPORATION
C08F212/08C08F2/48C08F299/00C08J3/075C08K5/005C08K5/10
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Quick Facts
Patent No.
US 11,692,048
App. No.
16/948,224
Granted
Jul 4, 2023
Kind
B2
Abstract

A gel composition is herein disclosed. According to one embodiment, the composition comprises a (i) a styrenic block copolymer, (ii) an oil; and (iii) optional additives; wherein the styrenic block copolymer has a structure ABi or iAB, wherein A is a monoalkenyl arene block, B is a conjugated diene block, and i is an isoprene attachment. The isoprene attachment i is substantially unsaturated and the conjugated diene block B is substantially saturated. The gel composition before curing exhibits thixotropic behavior, with a viscosity ranging from about 5000 mPa·s to about 30000 mPa·s. at 25° C. and a shear rate of 20 s −1 .

Claims (29)

1. A gel composition comprising: (i) a styrenic block copolymer, (ii) an oil; and (iii) optional additives:

wherein the styrenic block copolymer has a structure ABi or iAB, where

A is a monoalkenyl arene block,

B is a conjugated diene block,

i is an isoprene attachment,

the isoprene attachment i is substantially unsaturated and B is substantially saturated,

the monoalkenyl arene block has a molecular weight ranging from 35 kg/mol to 100 kg/mol;

wherein

the gel composition before curing is not solid, with a viscosity ranging from about 5000 mPa·s to about 30000 mPa·s. at 25° C. and a shear rate of 20 s −1 ; and

the gel composition after curing is solid.

2. The gel composition of claim 1 , wherein the styrenic block copolymer has a structure of ABi or iAB, and wherein the isoprene attachment i has a hydrogenation level of <50% and the conjugated diene B block has a hydrogenation level of >90%.

3. The gel composition of claim 2 , wherein the isoprene attachment i has a hydrogenation level of <40% and the conjugated diene B block has a hydrogenation level of >95%.

4. The gel composition of claim 3 , wherein the isoprene attachment i has a hydrogenation level of <35% and the conjugated diene B block has a hydrogenation level of >98%.

5. The gel composition of claim 1 , wherein at least 75% of double bonds present in the conjugated diene B block are hydrogenated.

6. The gel composition of claim 1 , wherein from about 20% to about 60% of the double bonds in the isoprene attachment i are hydrogenated.

7. The gel composition of claim 1 , wherein a difference in the hydrogenation level of the conjugated diene B block and the hydrogenation level of the isoprene attachment i is greater than about 20%.

8. The gel composition of claim 1 , wherein the styrenic block copolymer has a total residual unsaturation of from about 0.2 milliequivalents/gram to about 4 milliequivalents/gram.

9. The gel composition of claim 1 , wherein the monoalkenyl arene A block comprises styrene, alpha-methylstyrene, para-methylstyrene, vinyl toluene, vinylnaphthalene, diphenyl ethylene, para-butyl styrene, or mixtures thereof.

10. The gel composition of claim 1 , wherein the monoalkenyl arene A block has a polystyrene content of from about 15% to about 40%.

11. The gel composition of claim 1 , wherein the monoalkenyl arene A block has an apparent molecular weight of at least 40 kg/mol.

12. The gel composition of claim 1 , wherein the conjugated diene B block comprises conjugated 1,3-butadiene or conjugated substituted butadienes.

13. The gel composition of claim 1 , wherein the conjugated diene block B has an apparent molecular weight of from about 30 kg/mol to about 150 kg/mol.

14. The gel composition of claim 1 , wherein the isoprene attachment i has an apparent molecular weight of from about 2 kg/mol to about 15 kg/mol.

15. The gel composition of claim 1 , wherein the styrenic block copolymer further comprises less than 5 wt. % of a styrenic triblock copolymer based on the total weight of the styrenic block copolymer.

16. The gel composition of claim 1 , wherein the styrenic block copolymer is present in an amount of from about 1 wt. % to about 30 wt. % based on the total weight of the composition.

17. The gel composition of claim 1 , wherein the oil is present in an amount of from about 70 wt. % to about 99 wt. % based on the total weight of the composition, and wherein the oil comprises a paraffin, a mineral oil, a gas-to-liquid oil, a synthetic oil, or combinations thereof.

18. The gel composition of claim 1 , wherein the optional additives comprise an antioxidant, a metal deactivator, a curing accelerator, a rheology modifier, or combinations thereof.

19. The gel composition of claim 1 , wherein the gel composition is cured by any of UV irradiation, thermal treatment, or both, to form a solid gel after curing.

20. The gel composition of claim 12 , wherein the conjugated substituted butadiene is piperylene, 2,3-dimethyl-1,3-butadiene, 1-phenyl-1,3-butadiene or mixtures thereof.

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 30, 2021
From: MARIS, CATHERINE A.L.; MURPHY, ERIN B.; BENING, ROBERT C.; WEI, XIANGYUN; MUYLDERMANS, XAVIER D.
To: KRATON POLYMERS LLC
Reel/Frame 058505/0159 →
Continuity (3)
Continuation In Part 15916392 · Mar 9, 2018
Provisional Application 62469858 · Mar 10, 2017
Related Publication 20200399408A1 · Dec 24, 2020