Silicone-organic copolymer, sealants comprising same, and related methods

Patent metadata

Field	Value
Publication number	US-11807775-B2
Application number	US-201917416475-A
Country	US
Kind code	B2
Filing date	Dec 16, 2019
Priority date	Dec 21, 2018
Publication date	Nov 7, 2023
Grant date	Nov 7, 2023

Abstract

A silicone-organic copolymer has the formula Xg[ZjYo]c, where each X is an independently selected silicone moiety having a particular structure, each Y is an independently selected polyacrylate moiety, each Z is an independently selected siloxane moiety, subscript c is from 1 to 150, subscript g is >1, 0<j<2, and 0<o<2, with the proviso that j+o=2 in each moiety indicated by subscript c. Methods of preparing the silicone-organic copolymer are also disclosed. Further, a sealant is disclosed, the sealant comprising the silicone-organic copolymer and a condensation-reaction catalyst.

First claim

What is claimed is:

1. A silicone-organic copolymer having the formula:

wherein each Y comprises an independently selected organic moiety selected from polycarbonate moieties, polyester moieties, and polyacrylate moieties;
wherein each X is independently a silicone moiety having formula -D 1 -SiR 1 a (OR) 3−a ; where each D 1 is an independently selected divalent group; each R 1 is an independently selected substituted or unsubstituted hydrocarbyl group having from 1 to 18 carbon atoms; each R is an independently selected alkyl group having from 1 to 10 carbon atoms; and each subscript a is independently selected from 0 to 2;
wherein each subscript d is from 1 to 1000;
wherein subscript c is from 1 to 150; and
wherein each A is independently selected from a covalent bond, -D 2 -O—C(═O)—NH—, -D 2 -NH—C(═O)—NH—, -D 2 -NR 2 —CH 2 CH 2 C(═O)O—, and -D 2 -OC(═O)—CH 2 CH 2 NR 2 —, where D 2 is a divalent group and R 2 is H or R 1 , where R 1 is defined above.

2. The silicone-organic copolymer of claim 1 , wherein at least one Y comprises a second moiety different from the organic moiety.

3. The silicone-organic copolymer of claim 2 , wherein the second moiety is selected from an alkylaluminoxane moiety, an alkylgermoxane moiety, a polythioester moiety, a polyether moiety, a polythioether moiety, a polyester moiety, a polyacrylonitrile moiety, a polyacrylamide moiety, a polycarbonate moiety, a polyacrylate moiety, an epoxy moiety, a polyurethane moiety, a polyurea moiety, a polyacetal moiety, a polyolefin moiety, a polyvinyl alcohol moiety, a polyvinyl ester moiety, a polyvinyl ether moiety, a polyvinyl ketone moiety, a polyisobutylene moiety, a polychloroprene moiety, a polyisoprene moiety, a polybutadiene moiety, a polyvinylidiene moiety, a polyfluorocarbon moiety, a polychlorinated hydrocarbon moiety, a polyalkyne moiety, a polyamide moiety, a polyimide moiety, a polyimidazole moiety, a polyoxazole moiety, a polyoxazine moiety, a polyoxidiazole moiety, a polythiazole moiety, a polysulfone moiety, a polysulfide moiety, a polyketone moiety, a polyetherketone moiety, a polyanhydride moiety, a polyamine moiety, a polyimine moiety, a polyphosphazene moiety, a polysaccharide moiety, a polypeptide moiety, a polyisocyanate moiety, a cellulosic moiety, and combinations thereof.

4. A method of preparing a silicone-organic copolymer, said method comprising:
reacting an organic compound having on average more than one unsaturated group, a chain extending organosilicon compound having on average more than one silicon-bonded hydrogen atom, and an endcapping organosilicon compound, in the presence of a hydrosilylation catalyst to give the silicone-organic copolymer;
wherein the silicone-organic copolymer is the silicone-organic copolymer of claim 1 ; and
wherein A is the covalent bond.

5. The method of claim 4 , further comprising reacting a second compound having on average more than one unsaturated group with the organic compound, the chain extending organosilicon compound, and the endcapping organosilicon compound in the presence of the hydrosilylation catalyst.

6. The method of claim 4 , wherein the organic compound has the formula:
Y[R 2 ] i ,
wherein each R 2 is an independently an acrylate group or an unsaturated group having from 2 to 14 carbon atoms; subscript i is >1; and Y comprises an organic moiety selected from polycarbonate moieties, polyester moieties, and polyacrylate moieties.

7. The method of claim 4 , wherein the chain extending organosilicon compound comprises the linear silicon hydride functional organosilicon compound, and wherein the linear silicon hydride functional organosilicon compound has the formula:

wherein each R 1 is an independently selected substituted or unsubstituted hydrocarbyl group having from 1 to 18 carbon atoms; and each subscript d′ is from 1 to 999.

8. The method of claim 4 , wherein the endcapping organosilicon compound has the formula HSiR 1 a (OR) 3−a , where each R 1 is an independently selected substituted or unsubstituted hydrocarbyl group having from 1 to 18 carbon atoms; each R is an independently selected alkyl group having from 1 to 10 carbon atoms; and each subscript a is independently selected from 0 to 2.

9. A method of preparing a silicone-organic copolymer, said method comprising:
reacting an organic compound having one terminal unsaturated group and one terminal hydroxyl group with an endcapping organosilicon compound in the presence of a hydrosilylation catalyst to give a hydroxyl-functional intermediate;
reacting the hydroxyl-functional intermediate with a polyisocyanate to give an isocyanate-functional intermediate; and
reacting the isocyanate-functional intermediate and a chain extending organosilicon compound having two hydroxyl groups to give the silicone-organic copolymer;
wherein the silicone-organic copolymer is the silicone-organic copolymer of claim 1 ; and
wherein A is the covalent bond.

10. A method of preparing a silicone-organic copolymer, said method comprising:
reacting an organic compound having on average more than one hydroxyl group, a chain extending organosilicon compound having on average more than one hydroxyl group, a polyisocyanate compound, and an endcapping organosilicon compound having at least one isocyanate-functional group, to give the silicone-organic copolymer;
wherein the silicone-organic copolymer is the silicone-organic copolymer of claim 1 ; and
wherein A is selected from D 2 -O—C(═O)—NH—or -D 2 -NH—C(═O)—NH—, where D 2 is a divalent group and R 2 is H or R 1 , where R 1 is defined above.

11. A sealant, comprising:
a silicone-organic copolymer; and
a condensation reaction catalyst;
wherein the silicone-organic copolymer is the silicone-organic copolymer of claim 1 .

12. The sealant of claim 11 , further comprising: (i) a filler; (ii) a filler treating agent; (iii) a cross-linker; (iv) a surface modifier, (v) a drying agent; (vi) an extender; (vii) a biocide; (viii) a flame retardant; (ix) a plasticizer; (x) an end-blocker; (xi) a binder; (xii) an anti-aging additive; (xiii) a water release agent; (xiv) a pigment; (xv) a rheology modifier; (xvi) a carrier; (xvii) a tackifying agent; (xviii) a corrosion inhibitor; (xix) a catalyst inhibitor; (xx) an adhesion promotor; (xxi) a viscosity modifier; (xxii) a UV absorber; (xxiii) an anti-oxidant; (xxiv) a light-stabilizer; or (xxv) a combination of (i)-(xxiv); or optionally, further comprising a filler, a cross-linker, an extender, a plasticizer, and an adhesion promotor.

13. A cured product of the sealant of claim 11 .

14. A composite article comprising a substrate and the cured product of claim 13 disposed on the substrate.

15. A method of preparing a composite article, said method comprising:
disposing a sealant on a substrate; and
curing the sealant to give a cured product on the substrate, thereby forming the composite article;
wherein the sealant is the sealant of claim 11 .

16. A method of sealing a space defined between two elements, said method comprising:
applying a sealant to the space; and
curing the sealant in the space, thereby sealing the space;
wherein the sealant is the sealant of claim 11 .

Assignees

• Dow Silicones Corp
• Dow Global Technologies Llc

Inventors

• Duquesne Emmanuel
• Ferrito Michael S
• Grasmann Martin
• Harkness Brian
• Johnson William
• Krishnan Bindu
• Santos Elizabeth
• Scherzer Justin
• Young Jeanette
• Zhu Bizhong

Classifications

• C09D183/10 Primary

  Block or graft copolymers containing polysiloxane sequences (obtained by polymerising a compound having a carbon-to-carbon double bond on to a polysiloxane C09D151/08, C09D153/00) · CPC title

• C08G63/695

  containing silicon · CPC title

• C08G64/186

  containing polysiloxane sequences · CPC title

• C08G77/38

  Polysiloxanes modified by chemical after-treatment · CPC title

• C08G77/442 Primary

  containing vinyl polymer sequences · CPC title