Coating composition

Claim 2

Coating composition for application as one-coat system which comprises a. from 10 to 90 parts by weight of a low molecular weight polytetrafluorethylene having a melt viscosity of from 10 1 to 10 8 poises (measured at 380° C by means of the high pressure capillary viscometer), a specific surface of from 1 to 40 m 2 /g (measured according to the BET method), and a mean particle diameter of from 0.1 to 50 microns; b. from 90 to 10 parts by weight of a polymer containing triketo-imidazolidine rings and repeated units of the formula ##STR8## where R is a mono- to trinuclear, bi- to tetravalent aromatic radical, the aromatic radicals optionally being also quinones, and in polynuclear systems the aromatic radicals optionally being linked by aliphatic radicals or hetero atoms, furthermore the aromatic radicals optionally being mono- or polysubstituted by alkyl, cycloalkyl, alkoxy, aryl or monovalent functional radicals, R' is as defined for R or an aliphatic or cycloaliphatic hydrocarbon radical, n is an integer of from 1 to 70, and c. an aprotic organic solvent having a surface tension of more than 30 dyn/cm, in an amount by weight of from 0.43 to 100 times that of component b); up to 80% of the amount by weight of this aprotic solvent having a surface tension of more than 30 dyn/cm optionally being replaced by another organic solvent not meeting at least one of the two cited requirements, but necessarily having a boiling point at least 10° C lower than the boiling point of the aprotic solvent.

Claim 3

Coating composition for application as one-coat system which comprises a. from 10 to 90 parts by weight of a low molecular weight polytetrafluorethylene having a melt viscosity of from 10 1 to 10 8 poises (measured at 380° C by means of the high pressure capillary viscometer), a specific surface of from 1 to 40 m 2 /g (measured according to BET method), and a mean particle diameter of from 0.1 to 50 microns; b. from 90 to 10 parts by weight of a polymer containing triketo-imidazolidine rings and repeated units of the formula ##STR9## where R is a mono- to trinuclear, bi- to tetravalent aromatic radical, sthe aromatic radicals optionally being also quinones, and in polynulcear systems the aromatic radicals optionally being linked by aliphatic radicals or hetero atoms, furthermore the aromatic radicals optionally being mono- or polysubstituted by alkyl, cycloalkyl, alkoxy, aryl or monovalent functional radicals, R' is as defined for R or an aliphatic or cycloaliphatic hydrocarbon radical, R' optionally being interrupted by one or more of the following groups: b 1 . amide, imide and/or amidoimide groups, obtained by introduction of polycarboxylic acids, the ratio of the molar equivalents polycarboxylic acid : polyisocyanate being q : (q + 1), and q being from 1 to 40, b 21 . chelate forming azo or azomethine groups; b 22 . metal chelates of such azo or azomethine groups; the ratio of the molar equivalents of the oxamide acid ester to chelate-forming agents and/or metal chelates being (2 to 94) : (0.1 to 50), and the sum of oxamide acid ester, chelate-forming agent or chelate and possibly present polycarboxylic acids always being 100 mol %, n is an integer of from 1 to 70, and c. an aprotic organic solvent having a surface tension of more than 30 dyn/cm, is an amount by weight of from 0.43 to 100 times that of component (b); up to 80% of the amount by weight of this aprotic solvent having a surface tension of more than 30 dyn/cm optionally being replaced by another organic solvent not meeting at least one of the two cited requirements, but necessarily having a boiling point at least 10° C lower than the boiling point of the aprotic solvent.

Claim 4

Coating composition for application as one-coat system which comprises a. from 10 to 90 parts by weight of a low molecular weight polytetrafluorethylene having a melt viscosity of from 10 1 to 10 8 poises (measured at 380° C by means of the high pressure capillary viscometer), a specific surface of from 1 to 40 m 2 /g (measured according to BET method), and a mean particle diameter of from 0.1 to 50 microns; b. from 90 to 10 parts by weight of a polymer containing triketo-imidazolidine rings and repeated units of the formula ##STR9## where R is a mono- to trinuclear, bi- to tetravalent aromatic radical, sthe aromatic radicals optionally being also quinones, and in polynulcear systems the aromatic radicals optionally being linked by aliphatic radicals or hetero atoms, furthermore the aromatic radicals optionally being mono- or polysubstituted by alkyl, cycloalkyl, alkoxy, aryl or monovalent functional radicals, R' is as defined for R or an aliphatic or cycloaliphatic hydrocarbon radical, R' optionally being interrupted by one or more of the following groups: b 1 . amide, imide and/or amidoimide groups, obtained by introduction of polycarboxylic acids, the ratio of the molar equivalents polycarboxylic acid : polyisocyanate being q : (q + 1), and q being from 1 to 40, b 21 . chelate forming azo or azomethine groups; b 22 . metal chelates of such azo or azomethine groups; the ratio of the molar equivalents of the oxamide acid ester to chelate-forming agents and/or metal chelates being (2 to 94) : (0.1 to 50), and the sum of oxamide acid ester, chelate-forming agent or chelate and possibly present polycarboxylic acids always being 100 mol %, n is an integer of from 1 to 70, and c. an aprotic organic solvent having a surface tension of more than 30 dyn/cm, is an amount by weight of from 0.43 to 100 times that of component (b); up to 80% of the amount by weight of this aprotic solvent having a surface tension of more than 30 dyn/cm optionally being replaced by another organic solvent not meeting at least one of the two cited requirements, but necessarily having a boiling point at least 10° C lower than the boiling point of the aprotic solvent.

Claim 5

Coating composition as claimed in claim 1, wherein R is a radical of the formula ##STR10## where R"' is H or CH 3 , X is 0, S, CH 2 , SO 2 or zero, y is 1 or zero, z is from 1 to 3, or ##STR11##

Claim 6

Coating composition as claimed in claim 2, wherein R is a radical of the formula ##STR12## where R"' is H or CH 3 , X is 0, S, CH 2 , SO 2 or zero, y is 1 or zero, z is from 1 to 3, or ##STR13##

Claim 7

Coating composition as claimed in claim 1, wherein component (b) is prepared by reaction of oxamide acid esters of the formula R -- (NH -- CO -- COOR").sub.r and polyisocyanates of the formula R' -- N = C = O).sub.s in a molar ratio of oxamide acid ester : polyisocyanate of 1 : (0.8 to 2.2), the functionality of r and s being identical, R and R' being as defined in claim 1, R" being a hydrocarbon radical, r an integer of from 2 to 4 and s an integer of from 2 to 6.

Claim 8

Coating composition as claimed in claim 5, wherein r and s are 2.

Claim 9

Coating composition as claimed in claim 4, which comprises additionally introducing reaction products of polyisocyanates and polycarboxylic acids, the ratio of the molar equivalents polycarboxylic acid : polyisocyanate being q : (q + 1), and q = 1 to 40.

Claim 10

Coating composition as claimed in claim 2, which comprises using as chelate-forming structural unit as azomethine unit of the formula ##STR14## where R IV is a mono- or binuclear aromatic radical having from 6 to 14 carbon atoms containing an OH group in orthoposition to the azomethine group.

Claim 11

Coating composition as claimed in claim 2, which comprises using as chelate-forming structural unit an azo unit of the formula ##STR15## where R V is as defined in claim 8 for R IV .

Claim 12

Coating composition as claimed in claim 1, which comprises additionally up to 50 weight % relative to components (a) and (b) of usual fillers and/or pigments.

Claim 13

Coating composition as claimed in claim 2, which comprises additionally up to 50 weight % relative to components (a) and (b) of usual fillers and/or pigments

Claim 14

A process for the coating of surfaces, wherein the coating composition as claimed in claim 1 is used.

Claim 15

A process for the coating of surfaces, wherein the coating composition as claimed in claim 2 is used.

Claim 16

A process as claimed in claim 12, wherein the surface to be coated is made of metal, glass or ceramic materials.

Claim 17

A process as claimed in claim 13, wherein the surface to be coated is made of letal, glass or ceramic materials.