Solventless silicone pressure sensitive adhesive and methods for making and using same

Abstract

A solventless silicone pressure sensitive adhesive composition includes: (A) a polydiorganosiloxane having a monovalent hydrocarbon group with terminal aliphatic unsaturation, (B) a branched polyorganosiloxane having a monovalent hydrocarbon group with terminal aliphatic unsaturation, (C) a polyorganosilicate resin, (D) an olefinic reactive diluent, (E) a polyorganohydrogensiloxane, (F) a hydrosilylation reaction catalyst, and (G) an anchorage additive. This solventless silicone pressure sensitive adhesive composition can be cured to form a pressure sensitive adhesive. When cured on a backing substrate, the resulting adhesive article is useful for protecting electronic devices during fabrication, shipping, and use.

1 . A solventless silicone pressure sensitive adhesive composition comprising:
 (A) a polydiorganosiloxane comprising formula (A-1) (R 1   2 R 2 SiO)—(R 1   2 SiO) a —(OSiR 1   2 R 2 ), where each R 1  is independently selected from the group consisting of a monovalent hydrocarbon group free of terminal aliphatic unsaturation and a monovalent halogenated hydrocarbon group free of terminal aliphatic unsaturation, each R 2  is an independently selected monovalent hydrocarbon group with terminal aliphatic unsaturation, and subscript a has an average value of 150 to 2,000;   (B) a branched polyorganosiloxane comprising
 a Q branched polyorganosiloxane of unit formula (B-1) (R 1   3 SiO 1/2 ) g (R 1   2 R 2 SiO 1/2 ) h (R 1   2 SiO 2/2 ) i (SiO 4/2 ) j , where subscripts g, h, i, and j have average values such that 2≥g≥0, 4≥h≥0, 995≥i≥4, j=1, (g+h)=4, and a quantity (g+h+i+j) has a value sufficient to impart a viscosity >170 mPa·s to 1000 mPa·s at 25° C. as measured by rotational viscometry to the branched polyorganosiloxane, 
 a T branched polyorganosiloxane of unit formula (B-3) (R 1   3 SiO 1/2 ) d (R 2 R 1   2 SiO 1/2 ) e (R 1   2 SiO 2/2 ) m (R 1 SiO 3/2 ) n , where subscript d≥0, subscript e>0, subscript m is 15 to 995, and subscript n>0, or both (B-1) and (B-3); 
   where starting materials (A) and (B) are present in amounts sufficient to provide a molar ratio of starting material (B) to starting material (A) (B/A ratio) of 0.2/1 to 20/1;   (C) a polyorganosilicate resin comprising unit formula (C-1) (R 1   3 SiO 1/2 ) m (R 1   2 R 2 SiO 1/2 ) n (SiO 4/2 ) o , where subscripts m, n and o have average values such that m≥0, n≥0, o>1, and a quantity (m+n)>4,   where starting materials (A), (B) and (C) are present in amounts sufficient to provide a weight ratio of amount of starting material (C) to combined amounts of starting materials (A) and (B) (resin/polymer ratio) of 0.05/1 to 1.5/1;   (D) >0% to <5%, based on combined weights of all starting materials in the composition, of an olefinic reactive diluent;   (E) a polyorganohydrogensiloxane of unit formula (E-1) (R 1   3 SiO 1/2 ) p (R 1   2 SiO 2/2 ) q (R 1 SiO 3/2 ) r (SiO 4/2 ) s (R 1 HSiO 2/2 ) t (R 1   2 HSiO 1/2 ) u , where subscripts p, q, r, s, t, and u have values such that p≥0, q≥0, r≥0, s≥0, t≥0, u≥0, (t+u)≥2, and a quantity (p+q+r+s+t+u) is sufficient to provide the polyorganohydrogensiloxane with a degree of polymerization of 5 to 100; and   (F) a hydrosilylation reaction catalyst in an amount sufficient to provide 1 to 1000 ppm of platinum group metal based on combined weights of all starting materials in the composition; where the starting materials are present in amounts such that a molar ratio of silicon bonded hydrogen atoms to terminally aliphatically unsaturated groups (SiH/Vi) ratio is 1.5/1 to 10/1, based on combined molar amounts of all starting materials in the composition.   
     
     
         2 . The composition of  claim 1 , further comprising one or both of (G) 1% to 5%, based on combined weights of all starting materials in the composition, of an anchorage additive and (H) 0.05% to 1% of a hydrosilylation reaction inhibitor, based on combined weights of all starting materials in the composition. 
     
     
         3 . The composition of  claim 1 , where in formula (A-1) each R 1  is independently selected from the group consisting of methyl and phenyl, each R 2  is independently selected from the group consisting of vinyl, allyl and hexenyl; and subscript a has a value sufficient to impart viscosity of 450 mPa·s to <100,000 mPa·s to starting material (A). 
     
     
         4 . The composition of  claim 1 , where starting material (B) comprises formula (B-2):
 [R 2 R 1 Si—(O—SiR 1   2 ) x —O] y —Si—[O—(R 1   2 SiO) v SiR 1   3 ] w , where each R 1  is independently selected from the group consisting of methyl and phenyl, each R 2  is independently selected from the group consisting of vinyl, allyl, and hexenyl;   subscripts v, w, x, and y have values such that 200≥v≥1, 2≥w≥0, 200≥x≥1, 4≥y≥0, and a quantity (w+y)=4.   
     
     
         5 . The composition of  claim 1 , where starting material (C) comprises unit formula: (R 1   3 SiO 1/2 ) z (SiO 4/2 ) o , where each R 1  is independently selected from the group consisting of methyl and phenyl, subscript o is as described above, and subscript z>4. 
     
     
         6 . The composition of  claim 1 , where starting material (D) comprises 1% to 3% of an n-alkene of 14 to 16 carbon atoms. 
     
     
         7 . The composition of  claim 1 , where starting material (E) comprises unit formula (E-2):
 (R 1   3 SiO 1/2 ) 2 (R 1   2 SiO 2/2 ) aa (R 1 HSiO 2/2 ) bb , where each R 1  is selected from the group consisting of methyl and phenyl, subscript aa is 0 to 30, and subscript bb is 5 to 50.   
     
     
         8 . The composition of  claim 1 , where starting material (F) comprises Karstedt's Catalyst. 
     
     
         9 . The composition of  claim 2 , where starting material (G) comprises (G-1) vinyltriacetoxysilane, (G-2) glycidoxypropyltrimethoxysilane, or (G-3) a combination of (G-1) and (G-2). 
     
     
         10 . The composition of  claim 1 , where said composition has a viscosity of 300 mPa·s to 5,000 mPa·s at 25° C. as measured by rotational viscometry. 
     
     
         11 . A method for preparing an adhesive article comprising:
 1) coating the composition of  claim 1  on a surface of a backing substrate, and   2) curing the composition to form a pressure sensitive adhesive on the surface of the backing substrate.   
     
     
         12 . The method of  claim 11 , further comprising treating the backing substrate before coating the composition on the surface. 
     
     
         13 . The method of  claim 11 , further comprising: 3) adhering the pressure sensitive adhesive to an electronic device such that the pressure sensitive adhesive is between the backing substrate and the surface of the electronic device. 
     
     
         14 .- 15 . (canceled)