Silicone pressure-sensitive adhesive process and product thereof

• US 4,591,622 A
• Filed: 10/29/1984
• Issued: 05/27/1986
• Est. Priority Date: 10/29/1984
• Status: Expired due to Fees

• Current Assignee: Dow, Inc.
• Original Assignee: Dow, Inc.
• Inventors: Blizzard, John D., Swihart, Terence J.
• Primary Examiner(s): Briggs, Sr., Wilbert J.
• Application Number:
  US06/665,797
• Time in Patent Office: 575 Days
• Field of Search: 525/477, 525/478, 528/34, 524/588
• US Class Current: 525/477
• CPC Class Codes: C08G 77/44 containing only polysiloxane sequences
• CPC Class Codes: C09J 183/10 Block or graft copolymers containing polysiloxane sequences obtained by polymerising a compound having a carbon-to-carbon double bond on to a polysiloxane C09J151/08, C09J153/00

Abstract

This invention relates to silicone pressure-sensitive adhesives having improved viscosity stability and film physical property stability upon aging by a method comprising the condensation of a benzene-soluble resin copolymer of 0.6 to 0.9 triorganoxiloxy units per SiO_4/2 unit which contains silicon-bonded hydroxyl radicals and a polydiorganosiloxane preferably containing silicon-bonded hydroxyl or other hydrolyzable endblocking radicals with a sufficient amount of an endblocking agent containing endblocking triorganosilyl units such as hexamethyldisilazane or trimethylmethoxysilane to result in a 1:0.8 to 1:3 mole ratio of silicon-bonded hydroxyl radicals and hydrolyzable endblocking radicals to total moles of triorganosilyl units provided by the endblocking agent. The condensation is conducted, when desirable, in the presence of a catalytic amount of a mild silanol condensation catalyst if one is not provided by endblocking agent and when, necessary, in the presence of an effective amount of an organic solvent such as xylene. Condensation is preferably conducted with heating under solvent reflux conditions.

Claims

1. A method of making a silicone pressure-sensitive adhesive composition possessing improved stability upon aging which comprises the steps of:

(I) mixing

(A) from 40 to 70 inclusive parts by weight of at least one benzene-soluble resin copolymer containing silicon-bonded hydroxyl radicals and consisting essentially of R₃ SiO_1/2 units and SiO_4/2 units in a mole ratio of from 0.6 to 0.9 R₃ SiO_1/2 units for each SiO_4/2 unit present,

(B) from 30 to 60 parts by weight of at least one polydiorganosiloxane consisting essentially of ARSiO units terminated with endblocking TRASiO_1/2 units, each said polydiorganosiloxane having a viscosity of from 100 centipoise to 30,000,000 centipoise at 25°

C., and each T is R-- or X--,

(C) a sufficient amount of at least one organosilicon endblocking agent capable of generating an endblocking triorganosilyl unit selected from the group consisting of ZR₂ Si-- units, CH₃ Z'"'"'-- units, RZ"-- units and Z"'"'"'R₂ Si units to provide a 1;

0.8 to 1;

3 mole ratio of total silicon-bonded hydroxyl and X radicals present in said (A) and (B) to total endblocking triorganosilyl units provided by all endblocking agent present, said agent being selected from the group consisting of ZR₂ SiY, (ZR₂ Si)_q D, CH₃ Z'"'"'Y, (CH₃ Z'"'"')₂ O, RZ"Y'"'"', (RZ")₂ O and Z"'"'"'R₂ SiY'"'"',

(D) optionally, an additional catalytic amount of a mild silanol condensation catalyst, and

(E) when necessary, an effective amount of an organic solvent which is inert with respect to (A), (B), (C), and (D) to reduce the viscosity of a mixture of (A), (B), (C), and (D), and

(II) condensing the mixture of (A), (B), (C) and (D) at least until a substantial amount of the endblocking triorganosilyl units have reacted with the silicon-bonded hydroxyl radicals and X radicals of said (A) and (B),

wherein each R is a monovalent organic radical selected from the group consisting of hydrocarbon radicals of from 1 to 6 inclusive carbon atoms, each X radical is selected from the group consisting of HO--, H-- and R'"'"'O-- radicals, each R'"'"' is an alkyl radical of from 1 to 4 inclusive carbon atoms, each Y radical is a monovalent hydrolyzable organic radical or HO--, each Y'"'"' is HO-- or a monovalent hydrolyzable organic radical free of nitrogen, each A radical is selected from the group consisting of R-- and halohydrocarbon radicals of from 1 to 6 inclusive carbon atoms, each Z radical is A-- or QR"--, each R" is a divalent alkylene radical of from 1 to 6 inclusive carbon atoms, each Q is an organofunctional monovalent radical selected from the group consisting of RCOE'"'"', RE'"'"'OC--, NC--, R'"'"'E'"'"'--, HO--, G₂ N--, HO(R"O)_n --, and G₂ NCH₂ CH₂ NG--, where E'"'"' is --O--, --NG-- or --S--, n has a value of from 1 to 6,

Z'"'"' is ##STR8## Z" is ##STR9## Z"'"'"' is selected from the group consisting of HSR"--, HSCH₂ CH₂ NGR"-- and HOCH₂ CH₂ SR"-- radicals, each G is R-- or H--, D is a divalent or trivalent radical capable of being hydrolyzed to release said endblocking silyl units and q has a value of 2 when D is a divalent radical and q has a value of 3 when D is a trivalent radical.

2. The method as claimed in claim 1 wherein Y is selected from the group consisting of R'"'"'O--, HO--, Cl--, and G₂ N-- radicals, D is selected from the group consisting of --O--, --NG-- and --NHCONH--, said (A) is free of aliphatically unsaturated radicals when (B) contains such radicals and said (B) is free of aliphatically unsaturated radicals when (A) contains such radicals, and the endblocking agent of (C) is selected from the group consisting of ZR₂ SiY, (ZR₂ Si)₂ D, and mixtures thereof.

3. The method as claimed in claim 1 wherein said R₃ SiO_1/2 units present in said copolymer of (A) are (CH₃)₂ R"'"'"'SiO_1/2 units wherein each R"'"'"' is selected from the group consisting of methyl, vinyl, and phenyl radicals, said ARSiO units of (B) are selected from the group consisting of R"'"'"'₂ SiO units, (C₆ H₅)₂ SiO units and combinations of both, said TRASiO_1/2 endblocking units of (B) being of the unit formula (HO)R"'"'"'CH₃ SiO_1/2, at least 50 mole percent of the R"'"'"' radicals present in said (B) being methyl radicals and no more than 50 mole percent of the total moles of ARSiO units present in each polydiorganosiloxane of said (B) are (C₆ H₅)₂ SiO units, the endblocking agent of (C) is selected from the group consisting of ZR₂ SiY, (ZR₂ Si)₂ D and, mixtures thereof, D is selected from the group consisting of --O--, --NG-- and --NHCONH--, each Y radical is selected from the group consisting of R'"'"'O--, Cl--, HO-- and G₂ N--, each R present in said endblocking agent is selected from the group consisting of methyl and phenyl radicals and Z is selected from the group consisting of methyl, vinyl and 3,3,3-trifluoropropyl radicals, wherein (A) is free of aliphatically unsaturated radicals when (B) contains such radicals and (B) is free of aliphatically unsaturated radicals when (A) contains such radicals and wherein condensation step (II) is conducted at least until the rate of evolution of condensation reaction by-products is substantially constant.

4. The method as claimed in claim 3 wherein the mixture prepared in Step I further contains a hydrocarbon solvent selected from the group consisting of benzene, toluene and xylene and the condensation reaction of Step II is conducted with heating 80°

to 160°

C.

5. The method as claimed in claim 4 wherein no more than 10 mole percent of the R₃ SiO_1/2 units present in said (A) are (CH₃)₂ R""SiO_1/2 units, the remaining R₃ SiO_1/2 units are (CH₃)₃ SiO_1/2 units, said R"" radicals being methyl or vinyl radicals and no more than 10 mole percent of said ARSiO units of (B) being of the unit formula CH₃ R""SiO and the remaining ARSiO units present in said (B) are (CH₃)₂ SiO units, Z is a methyl or vinyl radical, the amount of said (A) being in the range of from 45 to 60 inclusive parts by weight, and the amount of said (B) being in the range of 40 to 55 inclusive parts by weight.

6. The method as claimed in claim 4 wherein the polydiorganosiloxane of (B) has a viscosity at 25°

C. of greater than 100,000 centipoise, the solvent being present in an amount which is such that the solvent comprises from 30 to 70 weight percent of the total weight of the mixture of (A), (B), (C), (D) and (E).

7. The method as claimed in claim 3 wherein the endblocking agent is (AR₂ Si)₂ NH, AR₂ SiOR'"'"' or AR₂ SiCl and no additional catalyst (D) is present in the mixture.

8. The method as claimed in claim 5 wherein the endblocking agent is (AR₂ Si)₂ NH, AR₂ SiOR'"'"' or AR₂ SiCl and no additional catalyst (D) is present in the mixture.

9. The method as claimed in claim 6 wherein the endblocking agent is (AR₂ Si)₂ NH, AR₂ SiOR'"'"' or AR₂ SiCl, Z is a methyl or vinyl radical and no additional catalyst (D) is present in the mixture.

10. The method as claimed in claim 1 wherein Step (I) comprises the Steps of (Ia) mixing (A), (B) and any (E) together in the presence of a silanol condensation catalyst, (Ib) condensing said (A) and (B) to form a condensed product and (Ic) mixing the product of Step (Ib) with (C), any (D) and any further amount of (E) which is necessary prior to proceeding with Step (II), said polydiorganosiloxane of (B) having a viscosity of from 100 to 100,000 centipoise at 25°

C.

11. The method as claimed in claim 3 wherein Step (I) comprises the Steps of (Ia) mixing (A), (B) and any (E) together in the presence of a silanol condensation catalyst, (Ib) condensing said (A) and (B) to form a condensed product and (Ic) mixing the product of Step (Ib) with (C), any (D) and any further amount of (E) which is necessary prior to proceeding with Step (II), said polydiorganosiloxane of (B) having a viscosity of from 100 to 100,000 centipoise at 25°

C.

12. The method as claimed in claim 5 wherein Step (I) comprises the Steps of (Ia) mixing (A), (B) and any (E) together in the presence of a silanol condensation catalyst, (Ib) condensing said (A) and (B) to form a condensed product and (Ic) mixing the product of Step (Ib) with (C), any (D) and any further amount of (E) which is necessary prior to proceeding with Step (II), said polydiorganosiloxane of (B) having a viscosity of from 100 to 100,000 centipoise at 25°

C.

13. The method as claimed in claim 11 wherein the endblocking agent is (AR₂ Si)₂ NH, AR₂ SiOR'"'"' or AR₂ SiCl.

14. The method as claimed in claim 12 wherein the endblocking agent is (AR₂ Si)₂ NH, AR₂ SiOR'"'"' or AR₂ SiCl.

15. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 1.

16. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 2.

17. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 3.

18. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 4.

19. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 5.

20. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 6.

21. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 7.

22. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 8.

23. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 9.

24. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 10.

25. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 11.

26. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 12.

27. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 13.

28. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 14.

29. A pressure-sensitive adhesive composition comprising a blend of the product obtained from the method of claim 1 with less than about 30 weight percent based on nonvolatile solids content of a modifier comprising from 1 to 100 parts by weight of a silicone resin copolymer consisting essentially of R₃ SiO_1/2 units and SiO_4/2 units in a mole ratio of from 0.6 to 0.9 R₃ SiO_1/2 units for each SiO_4/2 unit present and from 0 to 99 parts by weight of at least one polydiorganosiloxane consisting essentially of ARSiO units terminated with endblocking TRASiO_1/2 units, each said polydiorganosiloxane having a viscosity of from 100 centipoise to 30,000,000 centipoise at 25°

C.

30. A pressure-sensitive adhesive composition comprising a blend of the product obtained from the method of claim 3 with less than about 30 weight percent based on nonvolatile solids content of a modifier comprising from 1 to 100 parts by weight of a silicone resin copolymer consisting essentially of R₃ SiO_1/2 units and SiO_4/2 units in a mole ratio of from 0.6 to 0.9 R₃ SiO_1/2 units for each SiO_4/2 unit present and from 0 to 99 parts by weight of at least one polydiorganosiloxane consisting essentially of ARSiO units terminated with endblocking TRASiO_1/2 units, each said polydiorganosiloxane having a viscosity of from 100 centipoise to 30,000,000 centipoise at 25°

C.

31. A pressure-sensitive adhesive composition comprising a blend of the product obtained from the method of claim 5 with less than about 30 weight percent based on nonvolatile solids content of a modifier comprising from 1 to 100 parts by weight of a silicone resin copolymer consisting essentially of R₃ SiO_1/2 units and SiO_4/2 units in a mole ratio of from 0.6 to 0.9 R₃ SiO_1/2 units for each SiO_4/2 unit present and from 0 to 99 parts by weight of at least one polydiorganosiloxane consisting essentially of ARSiO units terminated with endblocking TRASiO_1/2 units, each said polydiorganosiloxane having a viscosity of from 100 centipoise to 30,000,000 centipoise at 25°

C.

32. A pressure-sensitive adhesive composition comprising a blend of the product obtained from the method of claim 6 with less than about 30 weight percent based on nonvolatile solids content of a modifier comprising from 1 to 100 parts by weight of a silicone resin copolymer consisting essentially of R₃ SiO_1/2 units and SiO_4/2 units in a mole ratio of from 0.6 to 0.9 R₃ SiO_1/2 units for each SiO_4/2 unit present and from 0 to 99 parts by weight of at least one polydiorganosiloxane consisting essentially of ARSiO units terminated with endblocking TRASiO_1/2 units, each said polydiorganosiloxane having a viscosity of from 100 centipoise to 30,000,000 centipoise at 25°

C.

33. The method as claimed in claim 1 wherein Y is R'"'"'O-- or Cl--.

34. A pressure-sensitive adhesive composition comprising the product obtained from the method of claim 33.