Air-water barrier silicone coatings

Abstract

The present application discloses a one-part room temperature vulcanizable (RTV) poly(diorganosiloxane) composition for a silicone elastomer air-water barrier coating for a building envelope; a method of preparing a silicone elastomer air-water barrier coating for a building envelope using such a composition and a building envelope prepared by such a method.

1 . A one-part room temperature vulcanizable (RTV) poly(diorganosiloxane) composition for a silicone elastomer air-water barrier coating for a building envelope, the composition comprising:
 (a) about 10-70 wt % of a poly(diorganosiloxane) of Formula I:   
       
         
           
           
               
               
           
         
         wherein
 R 1  and R 2  are each independently C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl, and 
 s an average value such that the viscosity of the poly(diorganosiloxane) of Formula I is from about 40,000-90,000 cP at 25° C.; 
 
         (b) about 5-40 wt % of a poly(diorganosiloxane) of Formula II: 
       
       
         
           
           
               
               
           
         
         wherein
 R 3  and R 4  are each independently C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl, 
 R 5a , R 5b , R 5c , R 5d , R 5e  and R 5f  are each independently C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl; and 
 q has an average value such that the viscosity of the poly(diorganosiloxane) of Formula II is from about 500-50,000 cP at 25° C.; 
 
         (c) about 0.5-25 wt % of an amorphous silica reinforcing filler; 
         (d) about 2-15 wt % of at least one cross-linking agent of Formula III:
   (X) 4-m —Si—R 6   m    (III),
 
 
         wherein
 R 6  is C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl; 
 m is 0, 1 or 2; and 
 X is a hydrolysable ketoximino-containing group of Formula IV: 
 
       
       
         
           
           
               
               
           
         
         
           
             wherein R 7a  and R 7b  are each independently C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl, or 
           
           X is a hydrolysable group of Formula V: 
         
       
       
         
           
           
               
               
           
         
         
           
             wherein R 8a , R 8b  and R 8c  are each independently H, C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl, 
           
         
         (e) about 0.2-5 wt % of an adhesion agent of Formula VI: 
       
       
         
           
           
               
               
           
         
         wherein
 R 9  and R 10  are each independently C 1-8 alkyl, C 2-8 alkenyl or C 6-10 aryl, 
 R 11  is C 1-10 alkyl, C 2-10 alkenyl or C 6-10 aryl, optionally substituted with one or more organofunctional groups; and 
 p is 0 or 1; and 
 
         (f) about 0.01-2 wt % of an organometallic condensation catalyst, wherein the metal of the organometallic condensation catalyst is selected from tin, titanium, zirconium, boron, zinc and bismuth, wherein each alkyl, alkenyl and aryl group in the compounds of Formula I, II, III, IV, V and VI is optionally halo-substituted. 
       
     
     
         2 . The composition of  claim 1 , wherein R 1  and R 2  are each methyl and n has an average value such that the viscosity of the poly(diorganosiloxane) of Formula I is from about 70,000-90,000 cP at 25° C. 
     
     
         3 . The composition of  claim 1 , wherein the poly(diorganosiloxane) of Formula I is present in an amount of about 20-40 wt %. 
     
     
         4 . The composition of  claim 1 , wherein R 3 , R 4 , R 5a , R 5b , R 5c , R 5d , R 5e  and R 5f  are each methyl and q has an average value such that the viscosity of the poly(diorganosiloxane) of Formula II is from about 500-1,500 cP at 25° C. 
     
     
         5 . The composition of  claim 1 , wherein the poly(diorganosiloxane) of Formula II is present in an amount of about 5-15 wt %. 
     
     
         6 . The composition of  claim 1 , wherein the amorphous silica reinforcing filler has a surface area of about 50-400 g/m 2  and a particle size range of about 0.01-0.03 microns. 
     
     
         7 . The composition of  claim 1 , wherein the amorphous silica reinforcing filler is surface treated with an organosilane, hexamethyldisilazane or polydimethylsiloxane. 
     
     
         8 . The composition of  claim 1 , wherein the amorphous silica reinforcing filler is present in an amount of about 1-5 wt %. 
     
     
         9 . The composition of  claim 1 , wherein the cross-linking agent is a cross-linking agent of Formula IIIa: 
       
         
           
           
               
               
           
         
       
       wherein R 6 , R 7a  and R 7b  are as defined in  claim 1 . 
     
     
         10 . The composition of  claim 1 , wherein the adhesion agent is an adhesion agent of Formula VIa:
   (R 9 O) 3 —Si—R 11    (VIa),
   
       wherein R 9  and R 11  are as defined in  claim 1 . 
     
     
         11 . The composition of  claim 10 , wherein R 9  is ethyl and R 11  is —(CH 2 ) 3 NH 2 . 
     
     
         12 . The composition of  claim 1 , wherein the organometallic condensation catalyst is dibutyltin dilaurate, dioctyltin di-(2-ethylhexanoate), dioctyltin dilaurate, lauryl stannoxane, dibutyltin diketonoate, dibutyltin diacetate, dibutyltin bis-(isooctyl maleate), dioctyltin dineodecanoate or dimethyltin dineodecanoate, or a mixture thereof. 
     
     
         13 . The composition of  claim 1 , wherein the organometallic condensation catalyst is present in an amount of about 0.05-0.5 wt %. 
     
     
         14 . The composition of  claim 1 , further comprising about 5-60 wt % of an extending filler selected from calcium carbonate, calcium silicate, barium sulfate, titanium dioxide, zirconium dioxide, chromium dioxide, antimony oxide, exfoliated graphite, quartz silica, diatomaceous earth, aluminum hydroxide, ceramic microspheres, hollow glass microspheres, hollow ceramic microspheres, fly ash, wollastonite, melamine, zinc borate, zinc oxides, iron oxide, titanium dioxide and mixtures thereof, each of which is optionally surface treated with an organosilane, hexamethyldisilazane or polydimethylsiloxane. 
     
     
         15 . The composition of  claim 1 , wherein the extending filler is stearic acid-treated calcium carbonate. 
     
     
         16 . The composition of  claim 14 , wherein the extending filler is present in an amount of about 20-30 wt %. 
     
     
         17 . The composition of  claim 1 , further comprising about 1-40 wt % solvent selected from an organic solvent and a methylated silicone solvent. 
     
     
         18 . A method of preparing a silicone elastomer air-water barrier coating for a building envelope, the method comprising:
 coating a substrate with a composition according to  claim 1 ; and   allowing the composition to cure under conditions to obtain the silicone elastomer air-water barrier coating.   
     
     
         19 . The method of  claim 18 , wherein the substrate comprises concrete, optionally coated with a sealant, drywall, oriented strand board (OSB), gypsum, fiberboard, chipboard, closed-cell extruded polystyrene foam, wood, stainless steel, carbon steel, galvanized steel, glass, metal cladding, aluminum, and coarse textured exterior insulation and finishing system (EIFS). 
     
     
         20 . A building envelope comprising a silicone elastomer air-water barrier coating prepared from the composition of  claim 1 .