End Use Applications Prepared From Certain Block Copolymers

• US 20090093584A1
• Filed: 10/09/2008
• Published: 04/09/2009
• Est. Priority Date: 10/09/2007
• Status: Abandoned Application

• Current Assignee: Kraton Polymers US LLC (DL Holdings Co., Ltd.)
• Original Assignee: Kraton Polymers US LLC (DL Holdings Co., Ltd.)
• Inventors: Gelles, Richard, Dubois, Donn Anthony, St. Clair, David John
• Application Number:
  US12/248,184
• Publication Number:
  US 20090093584A1
• Time in Patent Office: Days
• US Class Current: 524/505
• CPC Class Codes: C08F 297/026 polymerising acrylic acid, methacrylic acid or derivatives thereof
• CPC Class Codes: C08F 297/04 polymerising vinyl aromatic monomers and conjugated dienes
• CPC Class Codes: C08F 8/00 Chemical modification by after-treatment graft polymers, block polymers, crosslinking with unsaturated monomers or with polymers C08F251/00 - C08F299/00; of conjugated diene rubbers C08C
• CPC Class Codes: C08F 8/04 Reduction, e.g. hydrogenation
• CPC Class Codes: C08F 8/14 Esterification
• CPC Class Codes: C08F 8/48 Isomerisation; Cyclisation
• CPC Class Codes: C08L 2666/04 Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
• CPC Class Codes: C08L 2666/20 Macromolecular compounds having nitrogen in the main chain according to C08L75/00 - C08L79/00; Derivatives thereof
• CPC Class Codes: C08L 53/025 modified
• CPC Class Codes: C08L 75/04 Polyurethanes
• CPC Class Codes: C08L 9/06 Copolymers with styrene
• CPC Class Codes: C09J 153/005 Modified block copolymers
• CPC Class Codes: C09J 163/00 Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins

Abstract

The present invention relates to various end use applications prepared from certain block copolymers. The block copolymers include one or more A or A′ blocks or B blocks plus one or more terminal M blocks. Each A and A′ is a block or segment comprising predominantly a polymerized alkenyl aromatic compound, each B is a block or segment comprising predominantly a polymerized conjugated alkadiene, and each M is a six membered anhydride ring and/or acid group. The anhydride rings are prepared by thermally decomposing adjacent units of (1-methyl-1-alkyl)alkyl acrylic esters such as t-butylmethylacrylate. A wide variety of polymers are disclosed having the stable anhydride rings in the polymer backbone. The invention relates specifically to various end uses prepared from the reaction product of such block copolymers with various reactive resins, reactive monomers and metal derivatives.

Claims

1. A contact adhesive composition comprising a hybrid block copolymer, a resin and a solvent, wherein said hybrid block copolymer comprises the reaction product of (a) a base block copolymer having at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising six membered anhydride ring groups and acid groups, and (b) a reactive monomer or reactive resin or metal derivative that will react with the anhydride and/or acid groups of said end block.

2. The contact adhesive composition according to claim 1 wherein said base block copolymer prior to heating to form the anhydride rings and reaction with said reactive monomer or reactive resin or metal derivative comprises (a) a block of at least 80% by mole polymerized styrene, (b) a block of polymerized, hydrogenated butadiene having at least some 1,2-enchainments, or a block of polymerized, hydrogenated isoprene, or a block of polymerized, hydrogenated isoprene and butadiene and (c) a terminal block of polymerized t-butyl methacrylate polymerized through the ethylenic unsaturation thereof, wherein the block copolymer has the formula A-M, B-M, B-A-M, A-B-M or A-B-A′

-M wherein A and A′

are blocks of the polymerized aromatic styrene, B is the block of the hydrogenated, polymerized butadiene, isoprene or mixtures of butadiene and isoprene, and M is the terminal block of the polymerized t-butyl methacrylate, and wherein each block of the polymerized styrene has a number average molecular weight from about 2,000 to about 50,000, the block of the hydrogenated, polymerized diene has a number average molecular weight from about 20,000 to about 500,000, and the terminal M block has a number average molecular weight of 500 to about 100,000.

3. The contact adhesive composition of claim 2 wherein said reactive monomer is selected from the group consisting of isocyanate monomers, monomers with a hydroxy group, monomers with a glycidyl group and mixtures thereof, and said reactive resin is selected from the group consisting of phenolic resins, amino resins, epoxy resins and polyurethanes.

4. The contact adhesive composition of claim 3 wherein said block M of said hybrid block copolymer prior to reaction with said reactive monomer or reactive resin or metal derivative contains 0 to 20 wt % ester groups, 0 to 100 wt % anhydride groups and 0 to 50 wt % acid groups, based on the weight of the M block, the total of said ester groups, anhydride groups and acid groups equaling 100 wt % of block M.

5. The contact adhesive composition of claim 4 comprising 100 parts by weight of said base block copolymer, 20 to 500 parts by weight of a heat reactive phenolic resin, 1 to 10 parts by weight of a metal oxide and a solvent.

6. An adhesive composition comprising 100 parts by weight of at least one hybrid block copolymer, 25 to 300 parts by weight of at least one tackifying resin, 0 to 200 parts by weight of an extender oil, wherein said hybrid block copolymer comprises the reaction product of (a) at least one base block copolymer of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising six membered anhydride ring groups and acid groups, and (b) a reactive monomer or reactive resin that will react with the anhydride and/or acid groups of said end block.

7. The adhesive composition according to claim 6 wherein said base block copolymer prior to heating to form the anhydride rings and reaction with said reactive monomer or reactive resin comprises (a) a block of at least 80% by mole polymerized styrene, (b) a block of polymerized, hydrogenated butadiene having at least some 1,2-enchainments, or a block of polymerized, hydrogenated isoprene, or a block of polymerized, hydrogenated isoprene and butadiene and (c) a terminal block of polymerized t-butyl methacrylate polymerized through the ethylenic unsaturation thereof, wherein the block copolymer has the formula A-M, B-M, B-A-M, A-B-M or A-B-A′

-M wherein A and A′

are blocks of the polymerized aromatic styrene, B is the block of the hydrogenated, polymerized butadiene, isoprene or mixtures of butadiene and isoprene, and M is the terminal block of the polymerized t-butyl methacrylate, and wherein each block of the polymerized styrene has a number average molecular weight from about 2,000 to about 50,000, the block of the hydrogenated, polymerized diene has a number average molecular weight from about 20,000 to about 500,000, and the terminal M block has a number average molecular weight of 500 to about 100,000.

8. The adhesive composition according to claim 7 wherein said block M of said hybrid block copolymer prior to reaction with said reactive monomer or reactive resin contains 0 to 20 wt % ester groups, 0 to 100 wt % anhydride groups and 0 to 50 wt % acid groups, based on the weight of the M block, the total of said ester groups, anhydride groups and acid groups equaling 100 wt % of block M.

9. The adhesive composition according to claim 8 wherein said reactive monomer is selected from the group consisting of isocyanate monomers, monomers with a hydroxy group, monomers with a glycidyl group and mixtures thereof, said reactive resin is selected from the group consisting of phenolic resins, amino resins, epoxy resins and polyurethanes;

said tackifying resin is selected from the group consisting of hydrocarbon resins, rosin esters, rosin derivatives and mixtures thereof, said extender oil is selected from the group consisting of paraffinic and naphthenic oils and including a solvent selected from the group consisting of aromatic hydrocarbons, aliphatic hydrocarbons, polar oxygenated solvents, and mixtures thereof.

10. A toughened composition comprising a hybrid block copolymer, wherein said hybrid block copolymer comprises the reaction product of (a) a base block copolymer having at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising six membered anhydride ring groups and acid groups, and (b) a reactive resin selected from the group consisting of epoxy resins, polyisocyanates and amino resins.

11. The toughened composition according to claim 10 wherein said base block copolymer prior to heating to form the anhydride rings and reaction with said reactive resin comprises (a) a block of at least 80% by mole polymerized styrene, (b) a block of polymerized, hydrogenated butadiene having at least some 1,2-enchainments, or a block of polymerized, hydrogenated isoprene, or a block of polymerized, hydrogenated isoprene and butadiene and (c) a terminal block of polymerized t-butyl methacrylate polymerized through the ethylenic unsaturation thereof, wherein the block copolymer has the formula A-M, B-M, B-A-M, A-B-M or A-B-A′

-M wherein A and A′

are blocks of the polymerized aromatic styrene, B is the block of the hydrogenated, polymerized butadiene, isoprene or mixtures of butadiene and isoprene, and M is the terminal block of the polymerized t-butyl methacrylate, and wherein each block of the polymerized styrene has a number average molecular weight from about 2,000 to about 50,000, the block of the hydrogenated, polymerized diene has a number average molecular weight from about 20,000 to about 500,000, and the terminal M block has a number average molecular weight of 500 to about 100,000.

12. The toughened composition according to claim 11 wherein said reactive resin is an epoxy resin, said toughened composition comprising (a) from about 25 to 50 % w of said reactive epoxy resin, (b) from about 1 to 10% w of a block copolymer comprising a base block copolymer having at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising six membered anhydride ring groups and acid groups and (c) from about 40 to about 70% w of a reactive curing agent for the epoxy resin.

13. The toughened composition according to claim 11 wherein said reactive resin is an aromatic polyisocyanate, an aliphatic polyisocyanate or mixtures thereof, said toughened composition comprising (a) from about 50 to 90% w of a block copolymer comprising a base block copolymer having at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising six membered anhydride ring groups and acid groups, and (b) from about 10 to 50% w of said reactive resin.

14. The toughened composition according to claim 11 wherein said reactive resin is an amino resin selected from the group consisting of melamine-formaldehyde resins, glycoluril-formaldehyde resins and urea-formaldehyde resins, said toughened composition comprising (a) from about 60 to 90% w of a block copolymer comprising a base polymer having at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising six membered anhydride ring groups and acid groups, (b) about 10 to 40% w of an amino resin, and (c) about 0.01 to 3% w acid catalyst.

15. An acrylic composition comprising an acrylic copolymer reacted with a block copolymer, wherein said acrylic copolymer has a glass transition temperature below 0°

C. and contains at least one comonomer unit possessing a pendant reactive group capable of reacting with said block copolymer and wherein said block copolymer comprises at least one block of a polymerized conjugated diene and/or a polymerized alkenyl aromatic and at least one end block comprising a six membered anhydride ring and/or acid.

16. The acrylic composition of claim 15 wherein said acrylic composition is further reacted with an acrylic monomer selected from the group consisting of methyl acrylate, ethyl acrylate, isobutyl methacrylate, methyl methacrylate and mixtures thereof.

17. The acrylic composition of claim 16 wherein said acrylic copolymer is selected from the group consisting of (meth)acrylic ester/hydroxy(meth)alkyl ester copolymers, (meth)acrylic ester/glycidyl(meth)alkyl ester copolymers, (meth)acrylic ester/(meth)acrylic acid copolymers and (meth)acrylic ester/acrylamide copolymers

18. The acrylic composition according to claim 15 wherein said base block copolymer prior to heating to form the anhydride rings and reaction with said reactive monomer or reactive resin or metal derivative comprises (a) a block of at least 80% by mole polymerized styrene, (b) a block of polymerized, hydrogenated butadiene having at least some 1,2-enchainments, or a block of polymerized, hydrogenated isoprene, or a block of polymerized, hydrogenated isoprene and butadiene and (c) a terminal block of polymerized t-butyl methacrylate polymerized through the ethylenic unsaturation thereof, wherein the block copolymer has the formula A-M, B-M, B-A-M, A-B-M or A-B-A′

-M wherein A and A′

are blocks of the polymerized aromatic styrene, B is the block of the hydrogenated, polymerized butadiene, isoprene or mixtures of butadiene and isoprene, and M is the terminal block of the polymerized t-butyl methacrylate, and wherein each block of the polymerized styrene has a number average molecular weight from about 2,000 to about 50,000, the block of the hydrogenated, polymerized diene has a number average molecular weight from about 20,000 to about 500,000, and the terminal M block has a number average molecular weight of 500 to about 100,000.

19. The acrylic composition of claim 15, wherein said acrylic copolymer comprises (a) at least one alkyl acrylate monomer containing from about 4 to about 18 carbon atoms in the alkyl group, and (b) at least one monomer selected from the group consisting of methyl acrylate, ethyl acrylate, isobutyl methacrylate, vinyl acetate, methyl methacrylate, acrylonitrile, styrene, and mixtures thereof, and wherein said functionalized block copolymer comprises the reaction product of (i) a block copolymer comprising at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising a six membered anhydride ring and/or acid and (ii) at least one reactive monomer.

20. The acrylic composition of claim 19 wherein said reactive monomer is selected from the group consisting of hydroxy functional monomers, carboxy functional monomers, glycidyl functional monomers, acrylamide functional monomers, amine functional monomers, epoxy functional monomers, isocyanate functional monomers and mixtures thereof.

21. The acrylic composition of claim 20 wherein said acrylate monomer is selected from the group consisting of 2-ethyl hexyl acrylate, methyl acrylate, and hydroxy-ethyl acrylate.

22. The acrylic composition of claim 21 wherein said acrylic copolymer is crosslinked using a titanium crosslinking agent.

23. A functionalized block copolymer comprising the reaction product of (i) a block copolymer comprising at least one block of a polymerized conjugated diene or a polymerized alkenyl aromatic and at least one end block comprising a six membered anhydride ring and/or the acid formed from the reaction of this ring and water and (ii) at least one reactive component selected from the group consisting of functional monomers, acrylic copolymers containing a pendant reactive group, and reactive resins.

24. The functionalized block copolymer of claim 23 wherein (i) said functional monomer is selected from the group consisting of hydroxy functional monomers, carboxy functional monomers, glycidyl functional monomers, acrylamide functional monomers, amine functional monomers, epoxy functional monomers, isocyanate functional monomers and mixtures thereof;

(ii) said acrylic copolymer containing a pendant reactive group has a glass transition temperature below 10°

C.; and

(iii) said reactive resin is selected from the group consisting of phenolic resins, amino resins and epoxy resins.

25. The functionalized block copolymer of claim 23 wherein said base block copolymer prior to heating to form the anhydride rings and reaction with said reactive component comprises (a) a block of at least 80% by mole polymerized styrene, (b) a block of polymerized, hydrogenated butadiene having at least some 1,2-enchainments, or a block of polymerized, hydrogenated isoprene, or a block of polymerized, hydrogenated isoprene and butadiene and (c) a terminal block of polymerized t-butyl methacrylate polymerized through the ethylenic unsaturation thereof, wherein the block copolymer has the formula A-M, B-M, B-A-M, A-B-M or A-B-A′

-M wherein A and A′

are blocks of the polymerized aromatic styrene, B is the block of the hydrogenated, polymerized butadiene, isoprene or mixtures of butadiene and isoprene, and M is the terminal block of the polymerized t-butyl methacrylate, and wherein each block of the polymerized styrene has a number average molecular weight from about 2,000 to about 50,000, the block of the hydrogenated, polymerized diene has a number average molecular weight from about 20,000 to about 500,000, and the terminal M block has a number average molecular weight of 500 to about 100,000, and wherein said block M of said block copolymer prior to reaction with said functional monomer or acrylic copolymer or reactive resin contains 0 to 20 wt % ester groups, 0 to 100 wt % anhydride groups and 0 to 50 wt % acid groups, based on the weight of the M block.