IP Library Granted Patent US 11,427,710
Granted Patent B2
US 11,427,710 · App. 16/826,787 · Granted Aug 30, 2022

Compositions having reduced tack and articles made thereof

Inventor: Aaron Brothers (Houston, TX)
Assignee: KRATON POLYMERS LLC
C08L91/00B29C43/003B29C43/02B29C45/0001B29C45/0013B29K2025/08B29K2105/0061B29K2509/08B29K2995/0098C08L2205/03C08L2205/06
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Quick Facts
Patent No.
US 11,427,710
App. No.
16/826,787
Granted
Aug 30, 2022
Kind
B2
Abstract

A oil gel composition, consisting essentially of: 65-80 wt. % of a mineral oil, 15-25 wt. % of a hydrogenated styrenic block copolymer (HSBC), 1 to 15 wt. % of glass spheres having an average particle size of at least 15 microns, 1 at least 50 wt. % of a plasticizer selected from mineral oil, a paraffinic oil, an oil-enriched in paraffin, and mixtures thereof, and 0.25-5 wt. % of a tack reducing component selected from the group of steric acid, metal stearates, long chain fatty acids, fatty acid salts, fatty acid esters, amide waxes, ethylene-bis-stearamides, erucamide, polyester modified siloxanes, and mixtures thereof. The oil gel composition has an average peel strength of less than 0.3 lbf/in measured according to ASTM D 1876. Articles formed from the oil gel composition are characterized as being tack-free.

Claims (53)

1. An article molded from an oil gel composition consisting essentially of:

10-40 wt. % of a hydrogenated styrenic block copolymer (HSBC), having a general formula of A-B, A-B-A, A-B-A-B, (A-B-A)nX, (A-B)nX, or mixtures thereof, where each A block is a mono alkenyl arene polymer, each B block is a conjugated diene, n is an integer from 2 to 30, and X is a coupling agent residue;

up to 15 wt. % of a filler;

at least 50 wt. % of a plasticizer selected from mineral oil, a paraffinic oil, an oil-enriched in paraffin, and mixtures thereof;

0.25-5 wt. % of a tack reducing component selected from the group of stearic acid, metal stearates, long chain fatty acids, fatty acid salts, fatty acid esters, amide waxes, ethylene-bis-stearamides, erucamide, polyester modified siloxanes, and mixtures thereof, based on the total weight of the oil gel composition;

wherein the article is molded in a process without additional application of an external mold release surface coating or a powder coating to mold surface, and wherein the oil gel composition does not stick to the mold surface; and

wherein the article has an average peel strength of less than 53 N/m (0.3 lbf/in) according to modified ASTM D 1876.

2. The article of claim 1 , wherein the hydrogenated styrenic block copolymer comprises:

a tetra-branched block copolymer (IV) having a styrene equivalent peak molecular weight of 100,000 to 800,000 represented by the general formula (A-B) 4 X;

a tri-branched block copolymer (III) having a styrene equivalent peak molecular weight of from 75,000 to 600,000 represented by the general formula (A-B) 3 X;

a di-branched block copolymer (II) having a styrene equivalent peak molecular weight of from 50,000 to 400,000 represented by the general formula (A-B) 2 X; and

a linear diblock copolymer (I) having a styrene equivalent peak molecular weight of from 25,000 to 200,000 represented by the general formula A-B;

wherein:

A represents a polymer block of a mono alkenyl arene;

B represents a polymer block of a conjugated diene selected from the group consisting essentially of butadiene and mixtures of isoprene and butadiene;

X represents the residue of an alkoxy silane coupling agent having 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 aryl hydrocarbon radicals, linear alkyl hydrocarbon radicals and branched alkyl hydrocarbon radicals, and R′ is selected from linear and branched alkyl hydrocarbon radicals; and

wherein the relative amounts of copolymers I, II, III and IV are from 0 to 5 weight percent IV, from 0 to 60 weight percent III, from 40 to 95 weight percent II and from 2 to 10 weight percent 1, where the total of I, II, III and IV equals 100 weight percent.

3. The article of claim 1 , wherein the hydrogenated styrenic block copolymer is a styrene-ethylene-butylene-styrene (SEBS) or styrene-ethylene-ethylene-propylene-styrene (SEEPS) block copolymer.

4. The article of claim 1 , wherein the article is formed by any of injection molding, compression molding, rotomolding, thermoforming, casting, extrusion, profile extrusion, or blow molding.

5. The article of claim 1 , wherein the article is any of a mattress, a pillow, a mattress topper, a footwear cushion, an arm pad, a wrist or arm rest, a seating apparatus, a bedding product, upholstery, a pet bed, a medical cushioning foam, a seat cushion, an automotive foam, a sport cushion, a transportation cushion, a headrest, a personal protective equipment, or a toy.

6. The article of claim 1 , wherein the plasticizer is a mineral oil.

7. The article of claim 1 , wherein the tack reducing component is selected from stearic acid, fatty stearate salts, and mixtures thereof, and wherein the oil gel composition has an average peel strength of less than 35 N/m (0.2 lbf/in).

8. The article of claim 1 , wherein the tack reducing component is polycaprolactone-polydimethysiloxane block copolymer.

9. The article of claim 1 , wherein the tack reducing component is a lubricating grease selected from the group of organic fatty acids, esters, amides, and mixtures thereof, and wherein the lubricating grease has a drop melt point of at least 65° C., as defined by ASTM-127.

10. The article of claim 1 , wherein the tack reducing component is selected from ethylene-bis-stearamide, erucamide, or mixtures thereof.

11. A method of forming a molded article, the method comprising:

providing an oil gel composition has an average peel strength of less than 53 N/m (0.3 lbf/in) measured according to ASTM D 1876, the oil gel composition consists essentially of

10-40 wt. % of a hydrogenated styrenic block copolymer (HSBC), having a general formula A-B, A-B-A, A-B-A-B, (A-B-A)nX, (A-B)nX, or mixtures thereof, where each A block is a mono alkenyl arene polymer, each B block is a conjugated diene, n is an integer from 2 to 30, and X is a coupling agent residue;

1 to 15 wt. % of glass spheres having an average particle size of at least 15 microns;

at least 50 wt. % of a plasticizer selected from mineral oil, a paraffinic oil, an oil-enriched in paraffin, and mixtures thereof;

0.25-5 wt. % of a tack reducing component selected from the group of stearic acid, metal stearates, long chain fatty acids, fatty acid salts, fatty acid esters, amide waxes, ethylene-bis-stearamides, erucamide, polyester modified siloxanes, and mixtures thereof, based on the total weight of the oil gel composition;

injecting the oil gel composition into a mold to form the molded article without application of any mold release surface coating or a powder coating to mold surface; and wherein the oil gel composition does not stick to the mold surface.

12. The method of claim 11 , wherein providing the oil gel composition consists essentially of

forming a mixture with 10-40 wt. % of a hydrogenated styrenic block copolymer (HSBC), having a general formula A-B, A-B-A, A-B-A-B, (A-B-A)nX, (A-B)nX, or mixtures thereof, where each A block is a mono alkenyl arene polymer, each B block is a conjugated diene, n is an integer from 2 to 30, and X is a coupling agent residue;

1 to 15 wt. % of glass spheres having an average particle size of at least 15 microns; and

adding to the mixture

the at least 50 wt. % of a plasticizer selected from mineral oil, a paraffinic oil, an oil-enriched in paraffin, and mixtures thereof, and

the 0.25-5 wt. % of a tack reducing component selected from the group of stearic acid, metal stearates, long chain fatty acids, fatty acid salts, fatty acid esters, amide waxes, ethylene-bis-stearamides, erucamide, polyester modified siloxanes, and mixtures thereof, based on the total weight of the oil gel composition.

13. The method of claim 11 , wherein the hydrogenated styrenic block copolymer is a styrene-ethylene-butylene-styrene (SEBS) or styrene-ethylene-ethylene-propylene-styrene (SEEPS) block copolymer.

14. The method of claim 11 , wherein the hydrogenated styrenic block copolymer comprises:

a tetra-branched block copolymer (IV) having a styrene equivalent peak molecular weight of 100,000 to 800,000 represented by the general formula (A-B) 4 X;

a tri-branched block copolymer (III) having a styrene equivalent peak molecular weight of from 75,000 to 600,000 represented by the general formula (A-B) 3 X;

a di-branched block copolymer (II) having a styrene equivalent peak molecular weight of from 50,000 to 400,000 represented by the general formula (A-B) 2 X; and

a linear diblock copolymer (I) having a styrene equivalent peak molecular weight of from 25,000 to 200,000 represented by the general formula A-B;

wherein:

A represents a polymer block of a mono alkenyl arene;

B represents a polymer block of a conjugated diene selected from the group consisting essentially of butadiene and mixtures of isoprene and butadiene;

X represents the residue of an alkoxy silane coupling agent having 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 aryl hydrocarbon radicals, linear alkyl hydrocarbon radicals and branched alkyl hydrocarbon radicals, and R′ is selected from linear and branched alkyl hydrocarbon radicals; and

wherein the relative amounts of copolymers I, II, III and IV are from 0 to 5 weight percent IV, from 0 to 60 weight percent III, from 40 to 95 weight percent II and from 2 to 10 weight percent 1 , where the total of I, II, III and IV equals 100 weight percent.

15. The method of claim 11 , wherein the molding is any of injection molding, compression molding, rotomolding, or thermoforming.

16. The method of claim 11 , wherein the tack reducing component is polycaprolactone-polydimethysiloxane block copolymer.

17. The method of claim 11 , wherein the tack reducing component is selected from stearic acid, fatty stearate salts, or mixtures thereof.

18. An article formed by the method of claim 11 .

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 Sep 13, 2021
From: BROTHERS, AARON
To: KRATON POLYMERS LLC
Reel/Frame 057457/0935 →
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 →
Continuity (2)
Provisional Application 62830597 · Apr 8, 2019
Related Publication 20200317922A1 · Oct 8, 2020