IP Library Granted Patent US 7,357,960
Granted Patent B2
US 7,357,960 · App. 10/523,873 · Granted Apr 15, 2008

Silane-crosslinkable coating formulations

Assignee: Wacker Chemie AG
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Quick Facts
Patent No.
US 7,357,960
App. No.
10/523,873
Granted
Apr 15, 2008
Kind
B2
Abstract

The invention relates to coating formulations (B) which can be hardened to form coatings having a pencil hardness according to ISO 15184 of at least HB. Said formulations contain prepolymers (A) having alkoxysilane functions of general formula (6) —X—CH 2 —Si(OR)3- x R′ x , wherein R represents hydrogen, an alkyl, cycloalkyl or aryl radical respectively having between 1 and 6 atoms, and the carbon chain can be broken by non-adjacent oxygen, sulphur or NR″ groups; R′ represents an alkyl, cycloalkyl, aryl or arylalkyl radical respectively having between 1 and 12 C atoms, and the carbon chain can be broken by non-adjacent oxygen, sulphur or NR″ groups; R″ represents hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl, or aspartate acid ester radical; X represents oxygen, sulphur or a group of general formula (20) —O—CO—NR″—; and x represents 0 or 1.

Claims (92)

1. A process for preparing a coating on a substrate, comprising applying a coating formulation (B) which is curable to a coating having a pencil hardness according to ISO 15184 of at least HB, the coating formulation comprising at least one prepolymer (A) which bears alkoxysilane functionalities of the formula (6)

—X—CH 2 —Si(OR) 3-x R′ x   (6)

in which

R each, independently, is an alkyl, cycloalkyl or aryl radical having 1 to 6 carbon atoms, the carbon chain being uninterrupted or interrupted by non-adjacent oxygen, sulfur or NR″ groups,

R′ each, independently, is an alkyl, cycloalkyl, aryl or arylalkyl radical having 1 to 12 carbon atoms, the carbon chain being uninterrupted or interrupted by nonadjacent oxygen, sulfur or NR″ groups,

X is a group of the formula (20)

—O—CO—NR″—  (20)

wherein

R″ each, independently, is hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl or aspartate ester radical, and

x is 0 or 1,

wherein said prepolymers (A) are prepared by reaction of a silane

OCN—CH 2 —Si(OR) 3-x R′ x , with a

prepolymer precursor reactive therewith, and wherein the coating composition prepolymer (A) is neat or dissolved in solvent.

2. The process of claim 1 wherein the group R is a methyl or ethyl radical.

3. A process for preparing a coating on a substrate, comprising applying a coating formulation (B) which is curable to a coating having a pencil hardness according to ISO 15184 of at least HB, the coating formulation comprising at least one prepolymer (A) which bears alkoxysilane functionalities of the formula (6)

—X——CH 2 —Si(OR) 3-x R′ x   (6)

in which

R each, independently, is an alkyl, cycloalkyl or aryl radical having 1 to 6 carbon atoms, the carbon chain being uninterrupted or interrupted by non-adjacent oxygen, sulfur or NR″ groups,

R′ each, independently, is an alkyl, cycloalkyl, aryl or arylalkyl radical having 1 to 12 carbon atoms, the carbon chain being uninterrupted or interrupted by nonadjacent oxygen, sulfur or NR″ groups,

X is oxygen or a group of the formula (20)

—O—CO—NR″—  (20)

wherein

R″ each, independently, is hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl or aspartate ester radical, and

x is 0or 1,

wherein said prepolymers (A) are prepared by reaction of a silane selected from the group consisting of

CH 2 ═CW—CO—O—CH 2 Si(OR) 3-x R′ x ,

polyoxypropylene —O—CH 2 —Si(OR) 3-x R′ x , and

OCN—CH 2 —Si(OR) 3-x R′ x , with a

prepolymer precursor reactive therewith, and wherein the coating composition prepolymer (A) is neat or dissolved in solvent, and wherein W is H or CH 3 ,

wherein the coating formulations (B) further comprise at least one binder (D) bearing no alkoxysilane functionalities of the general formula (6).

4. A process for preparing a coating on a substrate, comprising applying a coating formulation (B) which is curable to a coating having a pencil hardness according to ISO 15184 of at least HB, the coating formulation comprising at least one prepolymer (A) which bears alkoxysilane functionalities of the formula (6):

—X—CH 2 —Si(OR) 3-x R′ x   (6)

in which

R each, independently, is an alkyl, cycloalkyl or aryl radical having 1 to 6 carbon atoms, the carbon chain being uninterrupted or interrupted by non-adjacent oxygen, sulfur or NR″ groups,

R′ each, independently, is an alkyl, cycloalkyl, aryl or arylalkyl radical having 1 to 12 carbon atoms, the carbon chain being uninterrupted or interrupted by nonadjacent oxygen, sulfur or NR″ groups,

X is oxygen or a group of the formula (20)

—O—CO—NR″—  (20)

wherein

R″ each, independently, is hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl or aspartate ester radical, and

x is 0 or 1,

wherein said prepolymers (A) are prepared by reaction of a silane selected from the group consisting of

CH 2 ═CW—CO—O—CH 2 Si(OR) 3-x R′ x ,

polyoxypropylene —O—CH 2 —Si(OR) 3-x R′ x , and

OCN—CH 2 —Si(OR) 3-x R′ x , with a

prepolymer precursor reactive therewith, and wherein the coating composition prepolymer (A) is neat or dissolved in solvent, and wherein W is H or CH 3 ,

wherein the coating formulation (B) is solvent-free.

5. A process for preparing a coating on a substrate, comprising applying a coating formulation (B) which is curable to a coating having a pencil hardness according to ISO 15184 of at least HB, the coating formulation comprising at least one prepolymer (A) which bears alkoxysilane functionalities of the formula (6)

—X—CH 2 —Si(OR) 3-x R′ x   (6)

in which

R each, independently, is an alkyl, cycloalkyl or aryl radical having 1 to 6 carbon atoms, the carbon chain being uninterrupted or interrupted by non-adjacent oxygen, sulfur or NR″ groups,

R′ each, independently, is an alkyl, cycloalkyl, aryl or arylalkyl radical having 1 to 12 carbon atoms, the carbon chain being uninterrupted or interrupted by nonadjacent oxygen, sulfur or NR″ groups,

X is oxygen or a group of the formula (20)

—O—CO—NR″—  (20)

wherein

R″ each, independently, is hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl or aspartate ester radical, and

x is 0 or 1,

wherein said prepolymers (A) are prepared by reaction of a silane selected from the group consisting of

polyoxypropylene —O—CH 2 —Si(OR) 3-x R′ x , and

OCN—CH 2 —Si(OR) 3-x R′ x ,

with a prepolymer precursor reactive therewith, and wherein the coating composition prepolymer (A) is neat or dissolved in solvent.

6. The coating of claim 5 , wherein at least one prepolymer precursor is selected from the group consisting of polyethers, polyesters, polyurethanes, polyureas, poly(meth)acrylates, polycarbonates, polystrenes, polysiloxane-urea/urethane copolymers, polyamides, polyvinyl esters, polyvinyl hydroxides, and polyolefins.

7. A process for preparing a coating on a substrate, comprising applying a coating formulation (B) which is curable to a coating having a pencil hardness according to ISO 15184 of at least HB, the coating formulation comprising at least one polyurethane prepolymer (A) which bears alkoxysilane functionalities of the formula (6)

—X—CH 2 —Si(OR) 3-x R′ x   (6)

in which

R each, independently, is an alkyl, cycloalkyl or aryl radical having 1 to 6 carbon atoms, the carbon chain being uninterrupted or interrupted by non-adjacent oxygen, sulfur or NR″ groups,

R′ each, independently, is an alkyl, cycloalkyl, aryl or arylalkyl radical having 1 to 12 carbon atoms, the carbon chain being uninterrupted or interrupted by nonadjacent oxygen, sulfur or NR″ groups,

X is oxygen or a group of the formula (20)

—O—CO—NR″—  (20)

wherein

R″ each, independently, is hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl or aspartate ester radical, and

x is 0 or 1.

8. The coating of claim 7 , prepared by reacting a hydroxyl-terminal polyurethane prepolymer with a silane of the formula

OCN—CH 2 —Si(OR) 3-x R′ x .

9. A process for preparing a coating on a substrate, comprising applying a coating formulation (B) which is curable to a coating having a pencil hardness according to ISO 15184 of at least HB, the coating formulation comprising at least one prepolymer (A) which bears alkoxysilane functionalities of the formula (6):

—X—CH 2 —Si(OR) 3-x R′ x   (6)

in which

R each, independently, is an alkyl, cycloalkyl or aryl radical having 1 to 6 carbon atoms, the carbon chain being uninterrupted or interrupted by non-adjacent oxygen, sulfur or NR″ groups,

R′ each, independently, is an alkyl, cycloalkyl, aryl or arylalkyl radical having 1 to 12 carbon atoms, the carbon chain being uninterrupted or interrupted by nonadjacent oxygen, sulfur or NR″ groups,

X is oxygen or a group of the formula (20)

—O—CO—NR″—  (20)

wherein

R″ each, independently, is hydrogen, an alkyl, cycloalkyl, aryl, aminoalkyl or aspartate ester radical, and

x is 0 or 1,

wherein said prepolymers (A) are prepared by reaction of a silane selected from the group consisting of

CH 2 ═CW—CO—O—CH 2 Si(OR) 3-x R′ x ,

polyoxypropylene —O—CH 2 —Si(OR) 3-x R′ x , and

OCN—CH 2 —Si(OR) 3-x R′ x , with a

prepolymer precursor reactive therewith, and wherein the coating composition prepolymer (A) is neat or dissolved in solvent, and wherein W is H or CH 3 , wherein the coating formulation is free of heavy metal catalysts.

10. The process of claim 9 , wherein the coating formulation (B) further comprises at least one reactive diluent which is a low molecular weight compound having a molecular weight such that the viscosity is not more than 5 Pas at 20° C. and which possesses reactive alkoxysilyl groups which are incorporated into a three-dimensional network as the coating cures.

11. The process of claim 10 , wherein at least one reactive diluent is selected from the group consisting of alkyltrimethoxysilanes, alkyltriethoxysilanes, vinyltrimethoxysilane, vinyltriethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, tetraethoxysilane, partial hydrolysates of these compounds, and compounds of the formulae (10) and (11)

R″—O—CH 2 —Si(OR) 3-x R′ x   (10),

R″—O—CO—NH—CH 2 —Si(OR) 3-x R′ x   (11).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2007
From: CONSORTIUM FUR ELEKTROCHEMISHE INDUSTRIE GMBH
To: WACKER CHEMIE AG
Reel/Frame 019728/0028 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2005
From: STANJEK, VOLKER; JUNG-ROSSETI, SILVA; SCHAUER, FELICITAS
To: CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH
Reel/Frame 016892/0377 →
Priority Claims (1)
DE 102 37 270 · Aug 14, 2002 · national
Continuity (1)
Related Publication 20050271885A1 · Dec 8, 2005