Silicon-containing materials with controllable microstructure

• US 8,840,965 B2
• Filed: 10/14/2011
• Issued: 09/23/2014
• Est. Priority Date: 10/15/2010
• Status: Expired due to Fees

• Current Assignee: Dow, Inc.
• Original Assignee: Dow, Inc.
• Inventors: Ahn, Dongchan, Beebe, Jeremy M.
• Primary Examiner(s): ZIMMER, MARC S
• Application Number:
  US13/822,226
• Publication Number:
  US 20130178549A1
• Time in Patent Office: 1,075 Days
• Field of Search: None
• US Class Current: 427/387
• CPC Class Codes: B05D 3/007 After-treatment
• CPC Class Codes: C08G 77/452 containing nitrogen-containing sequences
• CPC Class Codes: C08G 77/54 Nitrogen-containing linkages C08G77/485 takes precedence
• CPC Class Codes: C09D 183/08 containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
• CPC Class Codes: C09D 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 C09D151/08, C09D153/00
• CPC Class Codes: C09D 183/14 in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms C09D183/10 takes precedence

Abstract

In various embodiments, provided are silicon-containing coatings; silicon-containing coatings comprising microstructures that are responsive to one or more stimuli; oxidized products of said silicon-containing coatings; bulk solids; oxidized solids and powders; methods of preparing such coatings, solids, and powders; and substrates comprising the provided coatings.

Claims

1. A method of preparing silicon-containing materials, comprising:

(I) reacting an amine-reactive compound having at least one free-radical polymerizable group per molecule with a silane to form a reaction product, the silane having the formula;

(R¹₂NR²)_aSiR³_b(OR⁴)<sub>4−

(a+b)</sub>

wherein

a=1, 2, or 3;

b=0, 1, 2, or 3;

a+b=1, 2, 3, or 4;

each R¹ is independently selected from hydrogen, C1-C12 alkyl, halogen-substituted C1-C12 alkyl, C1-C12 cycloalkyl, aryl, nitrogen-substituted C1-C12 alkyl, and aliphatic ring structures which bridge the R¹ units, wherein the aliphatic ring structures are optionally N-substituted;

each R² is independently selected from C1-C30 alkyl;

each R³ is independently selected from hydrogen, halogen, C1-C12 alkyl, halogen-substituted C1-C12 alkyl, and —

OSiR^3′

₃, wherein R^3′

is selected from C1-C12 alkyl and halogen-substituted C1-C12 alkyl; and

each R⁴ is independently selected from hydrogen, C1-C12 alkyl, and halogen-substituted C1-C12 alkyl;

wherein a mole ratio of amine groups on the silane to amine-reactive groups on the amine-reactive compound is from 0.5 to 1.5;

wherein the reaction may optionally occur in the presence of at least one optional solvent to form a reaction product that is soluble in the at least one optional solvent; and

(II) combining the reaction product of (I) with an organoborane-organonitrogen complex in the presence of oxygen to form a polymer preparation,

wherein the polymer preparation of (II) is selected from (a) a solid;

(b) a liquid;

or if the reaction of (I) occurs in the presence of the at least one optional solvent, (c) a dispersion.

2. A method according to claim 1, further comprising forming a silicon-containing coating by (a) contacting at least one substrate surface with a polymer preparation of (II);

or (b) contacting at least one substrate surface with a polymer preparation of (II) dispersed in at least one solvent.

3. A method according to claim 2, further comprising forming an oxidized coating by (a) heating the silicon-containing coating;

(b) contacting the silicon-containing coating with at least one acid;

or (c) combinations thereof.

4. A method according to claim 3, wherein the oxidized coating is porous or substantially microporous.

5. A method according to claim 3, wherein the silicon-containing coating is heated to a temperature of from about 400°

C. to about 1000°

C.

6. A method according to claim 1, further comprising forming a bulk solid by heating a polymer preparation of (II), optionally under vacuum.

7. A method according to claim 1, further comprising forming an oxidized solid by (a) heating a polymer preparation of (II);

(b) contacting a polymer preparation of (II) with at least one acid;

or (c) combinations thereof.

8. A method according to claim 7, wherein the oxidized solid is porous or substantially microporous.

9. A method according to claim 6, further comprising forming an oxidized solid by (a) heating a bulk solid;

(b) contacting a bulk solid with at least one acid;

or (c) combinations thereof.

10. A method according to claim 9, wherein the oxidized solid is porous or substantially microporous.

11. A method according to claim 6, further comprising forming an oxidized powder by granulating a bulk solid to form a powder and (a) heating the powder formed, (b) contacting the powder formed with at least one acid, or (c) combinations thereof.

12. A method according to claim 1, wherein the reaction of (I) occurs in the presence of at least one solvent selected from toluene, xylene, linear siloxanes, cyclosiloxanes, hexamethyldisiloxane, octamethyltrisiloxane, pentamethyltetrasiloxane, ethyl acetate, propylene glycol methyl ether acetate, di(propyleneglycol)dimethyl ether, methylethyl ketone, methylisobutylketone, methylene chloride, tetrahydrofuran, 1,4-dioxane, N-methyl pyrollidone, N-methylformamide, dimethylsulfoxane, N,N-dimethylformamide, propylene carbonate, water, and any combination thereof.

13. A method according to claim 1, wherein the amine-reactive compound is selected from acrylic acid, methacrylic acid, 2-carboxyethylacrylate, 2-carboxyethylmethacrylate, acryloyl chloride, methacryloyl chloride, glycidyl acrylate, glycidyl methacrylate, and any combination thereof.

14. A method according to claim 1, wherein the silane is selected from aminomethyltriethoxysilane;

aminomethyltrimethoxysilane;

3-aminopropyltriethoxysilane;

3-aminopropyltrimethoxysilane;

3-aminopropylmethyldimethoxysilane;

3-aminopropylmethyldiethoxysilane;

3-aminopropylethyldimethoxysilane;

3-aminopropylethyldiethoxysilane;

3-aminopropyl dimethylmethoxysilane;

3-aminopropyldiethylmethoxysilane;

3-aminopropyl dimethylethoxysilane;

3-aminopropyldiethylethoxysilane;

n-butylaminopropyltrimethoxysilane;

4-aminobutyltriethoxysilane;

4-aminebutyltrimethoxysilane;

aminophenyltrimethoxysilane;

N,N-diethyl-3-aminopropyltrimethoxysilane;

N-(2-aminothyl)-3-aminopropyltrimethoxysilane;

3-aminopropyl trimethylsilane, m-aminophenyltrimethoxysilane, p-aminophenyltrimethoxysilane, 11-aminoundecyltriethoxysilane;

2-(4-pyridylethyl)triethoxysilane, 3-aminopropyltris(trimethylsiloxy)silane, and any combination thereof.

15. A method according to claim 1, wherein the organoborane-organonitrogen complex is a trialkylborane-organonitrogen complex selected from triethylborane-propanediamine, triethylborane-butylimidazole, triethylborane-methoxypropylamine, tri-n-butyl borane-methoxypropylamine, triethylborane-isophorone diamine, tri-n-butyl borane-isophorone diamine, triethylborane-aminosilanes, triethylborane-aminosiloxanes, and any combination thereof.

16. A silicon-containing coating prepared according to the method of claim 2, or

a silicon-containing coating prepared according to the method of claim 2, further comprising microstructures that are responsive to one or more stimuli.

17. An oxidized coating prepared according to the method of claim 3.

18. A bulk solid prepared according to the method of claim 6, comprising microstructures that are responsive to one or more stimuli.

19. A coated substrate comprising a substrate with at least one surface and the silicon-containing coating of claim 16 on at least one substrate surface.

20. A coated substrate comprising a substrate with at least one surface and the oxidized coating of claim 17 on at least one substrate surface.