Silicone pressure-sensitive adhesive process and product with improved lap-shear stability-II

• US 4,585,836 A
• Filed: 10/29/1984
• Issued: 04/29/1986
• Est. Priority Date: 10/29/1984
• Status: Expired due to Term

• Current Assignee: Dow, Inc.
• Original Assignee: Dow, Inc.
• Inventors: Homan, Gary R., Vincent, Harold L.
• Primary Examiner(s): Briggs, Sr., Wilbert J.
• Application Number:
  US06/665,796
• Time in Patent Office: 547 Days
• Field of Search: 525/477, 525/478, 528/34, 524/500, 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, film physical property stability upon aging and lap shear stability made by a method comprising the condensation of a benzene-soluble resin copolymer of 0.6 to 0.9 triorganosiloxy 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 ammonia releasing endblocking agent containing endblocking triorganosilyl units such as hexamethyldisilazane 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 with heating at 80° C.-160° C. in the presence of 0.1 to 10 moles of water per mole of ═NH present in the endblocking agent, 0.001 to 10 parts by weight per 100 parts by weight of total resin copolymer and polydiorganosiloxane and when necessary, in the presence of an effective amount of an organic solvent such as xylene. Condensation is preferably conducted under solvent reflux conditions. When the condensation reaction is substantially complete, the remaining endblocking agent, water, ammonia scavenger compound and ammonia released by the endblocking agent is stripped from the composition.

Claims

1. A method of making a silicone pressure-sensitive adhesive composition having improved lap shear stability which consists essentially of 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 of the formula

ZR₂ Si-- 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 SiNH₂ and (ZR ₂ Si)₂ NH,

(D) from 0.1 to 10 moles of water per mole of ═

NH provided by said (C),

(E) from 0.001 to 10 parts by weight per 100 parts by weight of (A) and (B) of at least one ammonia scavenger compound selected from the group consisting of HOC_m H_2m+1, HOC_x H_2x (OC_x H_2x)_y (O)_v H, C_w H_2w+1 (OC_x H_2x)_y OC_w H_2w+1, C_w H_2w+1 C(O) OC_n H_2n+1 and HC(O)OC_n H_2n+1, and

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

(II) condensing (A), (B) and (C) at a temperature of from 80°

C. to 160°

C. and at the same time at least periodically removing any condensation by-products from the mixture 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), and

(III) stripping substantially any remaining condensation by-products, (D) and (E) from the mixture after the condensation reaction of step II is substantially complete,

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, m has a value of from 2 to 4, n has a value of from 1 to 6, v is 0 or 1, w has a value of from 1 to 3, x has a value of from 2 to 6, y has a value of from 0 to 3, 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 --where E'"'"' is --O --, --NH-- or --S--, and each G is R'"'"'-- or H--,

2. The method as claimed in claim 1 wherein compound (E) is an alcohol of the formula HOC_m H_2m+1.

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, each R present in said endblocking agent (C) 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 radical, the condensation step (II) is conducted at least until the rate of evolution of condensation reaction by-products is substantially constant, and compound (E) is isopropanol.

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 under solvent reflux conditions to effect removal of said condensation by-products.

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, each 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), and (F).

7. The method as claimed in claim 3 wherein the endblocking agent is (AR₂ Si )₂ NH.

8. The method as claimed in claim 5 wherein the endblocking agent is (AR₂ Si)₂ NH.

9. The method as claimed in claim 6 wherein the endblocking agent is (AR₂ Si)₂ NH and each A is a methyl or vinyl radical.

10. The method as claimed in claim 1 wherein Step (I) comprises the Steps of (Ia) mixing (A), (B) and any (F) together, (Ib) condensing said (A) and (B) to form a condensed product and (Ic) mixing the product of Step (Ib) with (C), (D), (E) and any further amount of (F) 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 (F) together, (Ib) condensing said (A) and (B) to form a condensed product and (Ic) mixing the product of Step (Ib) with (C), (D), (E) and any further amount of (F) 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 (F) together, (Ib) condensing said (A) and (B) to form a condensed product and (Ic) mixing the product of Step (Ib) with (C), (D), (E) and any further amount of (F) 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 1 wherein Step (I) comprises the steps of (Ia) mixing (A), (B) and any (F) together, (Ib) adding said (C) to the mixture formed in step (Ia) to form a reaction mixture and (Ic) adding said (D) and (E) to the reaction mixture at a preselected point during said Step (II) prior to commencing Step (III).

14. The method as claimed in claim 3 wherein Step (I) comprises the steps of (Ia) mixing (A), (B) and any (F) together, (Ib) adding said (C) to the mixture formed in Step (Ia) to form a reaction mixture and (Ic) adding said (D) and (E) to the reaction mixture at a preselected point during said Step (IB) prior to commencing Step (III).

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.