Silicate Resins And Methods Of Preparing Same

Patent metadata

Field	Value
Publication number	US-2016289388-A1
Application number	US-201415037138-A
Country	US
Kind code	A1
Filing date	Dec 11, 2014
Priority date	Dec 23, 2013
Publication date	Oct 6, 2016
Grant date	—

Abstract

Provided in various embodiments are methods for making functional silicate MT′Q, MD′Q, and MM′Q resin compositions and the functional silicate resin compositions prepared by such methods. The functional silicate resin compositions may be used in, for example, coatings, rubbers, sealants, antifoams, paints, electronics, personal care items, medical devices and the like.

First claim

1 . A method of preparing a functional silicate resin comprising:
reacting (a) an MQ resin with (b) a trifunctional silane of the formula RSi(OR′) 3 in the presence of (c) a catalytic amount of a base to form an MT′Q resin having a general formula:
((CH 3 ) 3 SiO 1/2 ) m (RSiO 3/2 ) n (SiO 4/2 ) o
and, optionally, (d) an organic solvent,
wherein R is an organic functional group comprising an epoxy group, an acrylate group, a thiol group, an alkenyl group, a vinyl ether group, an amino group, a fluoro group, or any combination thereof; R′ is a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms; and m, n, o is the molar percent of each resin unit in the resin, m+n+o=1.

2 . A method of preparing a functional silicate resin comprising:
reacting (a) an MQ resin with (b) a difunctional silane of the formula RR″Si(OR′) 2 in the presence of (c) a catalytic amount of a base to form an MD′Q resin having a general formula:
((CH 3 ) 3 SiO 1/2 ) m (RR″SiO 2/2 ) n (SiO 4/2 ) o

and, optionally, (d) an organic solvent,
wherein R is an organic functional group comprising an epoxy group, an acrylate group, a thiol group, an alkenyl group, a vinyl ether group, an amino group, a fluoro group, or any combination thereof; R′ is a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms, R″ is an alkyl or aryl group having 1-20 carbon atoms; and m, n, o is the molar percent of each resin unit in the resin, m+n+o=1.

3 . A method of preparing a functional silicate resin comprising:
reacting (a) an MQ resin with (b) a monofunctional silane of the formula RR″ 2 Si(OR′) in the presence of (c) a catalytic amount of a base to form an MM′Q resin having a general formula:
((CH 3 ) 3 SiO 1/2 ) m (RR″ 2 SiO 1/2 ) n (SiO 4/2 ) o

and, optionally, (d) an organic solvent,
wherein R is an organic functional group comprising an epoxy group, an acrylate group, a thiol group, an alkenyl group, a vinyl ether group, an amino group, a fluoro group, or any combination thereof; R′ is a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms; each R″ is independently an alkyl or aryl group having 1-20 carbon atoms; and m, n, o is the molar percent of each resin unit in the resin, m+n+o=1.

4 . The method according to claim 1 , wherein the MQ resin has the formula:
((CH 3 ) 3 SiO 1/2 ) m (SiO 4/2 ) o
wherein m, o is the molar percent of each resin unit in the resin, m+o=1, and the molar ratio of m/o is in the range of from about 0.1/1 to about 2/1.

5 . The method according to claim 1 , wherein the base includes potassium hydroxide, sodium hydroxide, cesium hydroxide, potassium methoxide, sodium methoxide, cesium methoxide, tetramethylammonium hydroxide, pyridine, methyl amine, imidazole, benzimidazole, histidine, phosphazene, or any combination thereof.

6 . The method according to claim 1 , wherein the organic solvent includes toluene, xylene, propylene glycol monomethyl ether acetate, 2-butanone, ethyl acetate, butyl acetate, acetonitrile, benzene, cyclohexane, dioxane, diethyl ether, tetrahydrofuran, hexane, or any combination thereof.

7 . The method according to claim 1 , wherein R is an organic functional group comprising an epoxy group, wherein the epoxy group is a 3-glycidoxypropyl group or a 2-(3,4-epoxycyclohexyl)ethyl group.

8 . The method according to claim 1 , wherein R is an organic functional group comprising an acrylate group, wherein the acrylate group contains the structural unit CH 2 ═CHR 3 —COO—, wherein R 3 is hydrogen, an alkyl group or an aryl group.

9 . The method according to claim 1 , wherein R is an organic functional group comprising a thiol group, wherein the thiol group is
HS—Z—SiR″ n (OR′) 3-n

wherein Z is a hydrocarbon chain, including but not limited to, —CH 2 —, —(CH 2 ) 2 —, (CH 2 ) 3 —, —(CHMe-CH 2 CH 2 )—, and —(CH 2 ) 4 —; n=0, 1, or 2; R′ is a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms; and each R″ is independently an alkyl or aryl group having 1-20 carbon atoms.

10 . The method according to claim 1 , wherein R is an organic functional group comprising an alkenyl group, wherein the alkenyl group is H 2 C═CH—, H 2 C═CHCH 2 —, H 2 C═C(CH 3 )CH 2 —, H 2 C═CHCH 2 CH 2 —, H 2 C═CHCH 2 CH 2 CH 2 —, H 2 C═CHCH 2 CH 2 CH 2 CH 2 —, or any combination thereof.

11 . The method according to claim 1 , wherein R is an organic functional group comprising a vinyl ether group.

12 . The method according to claim 1 , wherein R is an organic functional group comprising an amino group, wherein the amino group contains the structural unit R 3 N—, wherein R 3 is hydrogen, an alkyl group, or an aryl group.

13 . The method according to claim 1 , wherein the reaction is conducted at temperature ranging from about 23° C. to about 150° C.

14 . The method according to claim 1 , wherein the amount of base in the functional silicate resin ranges from about 0.01 wt. % to about 1 wt. %.

15 . The functional silicate resin prepared by the method of claim 1 .

16 . A functional silicate resin having a general formula:
((CH 3 ) 3 SiO 1/2 ) m (RSiO 3/2 ) n (SiO 4/2 ) o
wherein R is an organic functional group comprising an epoxy group, an acrylate group, a thiol group, an alkenyl group, a vinyl ether group, an amino group, a fluoro group, or any combination thereof; and m, n, o is the molar percent of each resin unit in the resin, m+n+o=1.

17 . The functional silicate resin of claim 16 , wherein the functional silicate resin is
((CH 3 ) 3 SiO 1/2 ) m [(R 1 SiO 3/2 ) x (R 2 SiO 3/2 ) y ] n (SiO 4/2 ) o
wherein R 1 and R 2 are each independently an epoxy group, an acrylate group, an alkenyl group, a thiol group, a vinyl ether group, or any combination thereof; m, n, o is the molar percent of each resin unit in the resin, m+n+o=1; and x+y=n.

18 . A functional silicate resin having a general formula:
((CH 3 ) 3 SiO 1/2 ) m (RR″SiO 2/2 ) n (SiO 4/2 ) o

wherein R is an organic functional group comprising an epoxy group, an acrylate group, a thiol group, an alkenyl group, a vinyl ether group, an amino group, a fluoro group, or any combination thereof; R″ is an alkyl or aryl group having 1-20 carbon atoms; and m, n, o is the molar percent of each resin unit in the resin, m+n+o=1.

19 . A functional silicate resin having a general formula:
((CH 3 ) 3 SiO 1/2 ) m (RR″ 2 SiO1/2) n (SiO 4/2 ) o

wherein R is an organic functional group comprising an epoxy group, an acrylate group, a thiol group, an alkenyl group, a vinyl ether group, an amino group, a fluoro group, or any combination thereof; each R″ is independently an alkyl or aryl group having 1-20 carbon atoms; and m, n, o is the molar percent of each resin unit in the resin, m+n+o=1.

Assignees

• Dow Corning

Inventors

• Fu Peng-Fei
• Moyer Eric

Classifications

• C09D183/04

  Polysiloxanes · CPC title

• C08G77/20

  containing silicon bound to unsaturated aliphatic groups · CPC title

• C08G77/26

  nitrogen-containing groups · CPC title

• C08G77/08 Primary

  characterised by the catalysts used · CPC title

• C08G77/38

  Polysiloxanes modified by chemical after-treatment · CPC title