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US4101487A Expired / Lapsed US ⏱️ 0.0 years remaining

Coating medium

Assignee: General Electric Co
•
Filing: 1976-08-13
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Granted: 1978-07-18
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Expires: 1996-08-13
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Abstract

Abstract A heat curable coating medium for use in the formation of a cured, highly cross-linked, polymeric coating on a substrate. The coating medium comprises an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and an aromatic dianhydride, in the molar ratio of two-to-one respectively, in a solvent.

Inventors

  • 👤 Marvin A. Peterson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 15:15
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1067; C08G73/1071; C08G73/1046; C08G73/1057; C08G73/1064; C08G73/1075; C08G73/1082; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31678; Y10T428/31681; Y10T428/31721

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 77 words
A heat curable coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and an aromatic dianhydride, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, in an inert solvent for at least one of said reactants, a coating of said medium on a substrate being heat curable at imidization temperature to form a cured highly cross-linked polymeric coating thereon.
Claim 2
Dependent Claim 77 words
A heat curable coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and an aromatic dianhydride, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, in an inert solvent for at least one of said reactants, a coating of said medium on a substrate being heat curable at imidization temperature to form a cured highly cross-linked polymeric coating thereon.
Claim 3
Dependent Claim 115 words
A coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and an aromatic dianhydride, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, a volatile base, and an aqueous-organic solvent medium wherein the organic portion of said solvent medium is a water miscible inert solvent for at least one of said reactants, said reaction product being heat curable at imidization temperature after application of said coating medium as a thin film coating on a substrate, to form a highly cross-linked polymeric coating including imide groups, amide groups and amine groups and being substantially free of carboxyl groups.
Claim 4
Dependent Claim 115 words
A coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and an aromatic dianhydride, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, a volatile base, and an aqueous-organic solvent medium wherein the organic portion of said solvent medium is a water miscible inert solvent for at least one of said reactants, said reaction product being heat curable at imidization temperature after application of said coating medium as a thin film coating on a substrate, to form a highly cross-linked polymeric coating including imide groups, amide groups and amine groups and being substantially free of carboxyl groups.
Claim 5
Dependent Claim 90 words
The coating medium defined in claim 2 wherein: said dianhydride is selected from the group consisting of: 4,4'-(2-acetoxy-1,3-glyceryl)bis-anhydro trimellitate, 3,3', 4,4'-benzophenonetetracarboxylic dianhydride, bis(3,4-dicarboxyphenyl) sulfone dianhydride, bis(2,3-dicarboxyphenyl) methane dianhydride, 2,2-bis (3,4-dicarboxyphenyl)propane dianhydride, bis (3,4-dicarboxyphenyl)ether dianhydride, 2,2-bis(2,3-dicarboxyphenylpropane dianhydride, 1,1-bis(2,3-dicarboxyphenyl)ethane dianhydride, 1,1-bis(3,4-dicarboxyphenyl)ethane dianhydride, and the like. and said diamine is selected from the group consisting of: meta-phenylene diamine, para-phenylenediamine, 4,4'-diamino-diphenyl propane, 4,4'-diamino-diphenyl methane, benzidine, 4,4'-diamino-diphenyl sulfide, 4,4'-diamino-diphenyl sulfone, 3,3'-diamino-diphenyl sulfone, 4,4'-diamino-diphenyl ether, 2,6-diamino-pyridine, bis-(4-amino-phenyl)diethyl silane, bis-(4-amino-phenyl) phosphine oxide, bis-(4-amino-phenyl)-N-methylamine, 1,5-diamino naphthalene, 3,3'-dimethyl-4,4'-diamino-biphenyl, 3,3'-dimethoxy benzidine, m-xylene diamine, p-xylene diamine, 1,3-bis-delta-amino-butyltetramethyl disiloxane, and 1,3-bis-gamma-aminopropyltetraphenyl disiloxane.
Claim 6
Dependent Claim 39 words
The coating medium defined in claim 2 wherein: said diamine is selected from the group consisting of 4,4'-diaminodiphenyl methane, 4,4'-diaminodiphenyl ether, and 1,3-diamino benzene, and said dianhydride is selected from the group consisting of 3,3',4,4'-benzophenonetetracarboxylic dianhydride and 4,4'-(2-acetoxy-1,3-glyceryl)bis-anhydro trimellitate.
Claim 7
Dependent Claim 77 words
A heat curable coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and a tetracarboxylic compound, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, in a inert solvent for at least one of said reactants, a coating of said medium on a substrate being heat curable at imidizaton temperature to form a cured highly cross-linked polymeric coating thereon.
Claim 8
Dependent Claim 77 words
A heat curable coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and a tetracarboxylic compound, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, in a inert solvent for at least one of said reactants, a coating of said medium on a substrate being heat curable at imidizaton temperature to form a cured highly cross-linked polymeric coating thereon.
Claim 9
Dependent Claim 115 words
A coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and a tetracarboxylic compound, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, a volatile base, and an aqueous-organic solvent medium wherein the organic portion of said solvent medium is a water miscible inert solvent for at least one of said reactants, said reaction product being heat curable at imidization temperature after application of said coating medium as a thin film coating on a substrate, to form a highly cross-linked polymeric coating including imide groups, amide groups and amine groups and being substantially free of carboxyl groups.
Claim 10
Dependent Claim 115 words
A coating medium comprising an aromatic diamide diacid diamine formed as the reaction product of an aromatic diamine and a tetracarboxylic compound, in the molar ratio of two-to-one respectively, at a temperature below that at which more than negligible imidization occurs, a volatile base, and an aqueous-organic solvent medium wherein the organic portion of said solvent medium is a water miscible inert solvent for at least one of said reactants, said reaction product being heat curable at imidization temperature after application of said coating medium as a thin film coating on a substrate, to form a highly cross-linked polymeric coating including imide groups, amide groups and amine groups and being substantially free of carboxyl groups.
Claim 11
Dependent Claim 37 words
The coating medium defined in claim 6 wherein: said tetracarboxylic compound is a dianhydride selected from the group consisting of: 4,4'-(2-acetoxy-1,3-glyceryl)bis-anhydro trimellitate, 3,3'-4,4'-benzophenonetetracarboxylic dianhydride, bis(3,4-dicarboxyphenyl) sulfone dianhydride, bis(2,3-dicarboxyphenyl) methane dianhydride, 2,2-bis (3,4-dicarboxyphenyl)propane dianhydride, bis (3,4-dicarboxyphenyl) ether dianhydride,
Claim 12
Dependent Claim 57 words
2-bis(2,3-carboxyphenyl)propane dianhydride, 1,1-bis(2,3-dicarboxyphenyl)ethane dianhydride, 1,1-bis(3,4-dicarboxylphenyl)ethane dianhydride, and the like, and said diamine is selected from the group consisting of: meta-phenylene diamine, para-phenylenediamine, 4,4'-diamino-diphenyl propane, 4,4'-diamino-diphenyl methane, benzidine, 4,4'diamino-diphenyl sulfide, 4,4'-diamino-diphenyl sulfone, 3,3'-diamino-diphenyl sulfone, 4,4'-diamino-diphenyl ether, 2,6-diamino-pyridine, bis-(4-amino-phenyl) diethyl silane, bis-(4-amino-phenyl) phosphine oxide, bis-(4-amino-phenyl-N-methylamine, 1,5-diamino naphthalene, 3,3'-dimethyl-4,4'-diamino-biphenyl, 3,3'-dimethoxy benzidine, m-xylylene diamine, p-xylyene diamine, 1,3-bis-delta-amino-butyltetramethyl disiloxane, and 1,3-bis-gamma-aminopropyltetraphenyl disiloxane.
Claim 13
Dependent Claim 57 words
2-bis(2,3-carboxyphenyl)propane dianhydride, 1,1-bis(2,3-dicarboxyphenyl)ethane dianhydride, 1,1-bis(3,4-dicarboxylphenyl)ethane dianhydride, and the like, and said diamine is selected from the group consisting of: meta-phenylene diamine, para-phenylenediamine, 4,4'-diamino-diphenyl propane, 4,4'-diamino-diphenyl methane, benzidine, 4,4'diamino-diphenyl sulfide, 4,4'-diamino-diphenyl sulfone, 3,3'-diamino-diphenyl sulfone, 4,4'-diamino-diphenyl ether, 2,6-diamino-pyridine, bis-(4-amino-phenyl) diethyl silane, bis-(4-amino-phenyl) phosphine oxide, bis-(4-amino-phenyl-N-methylamine, 1,5-diamino naphthalene, 3,3'-dimethyl-4,4'-diamino-biphenyl, 3,3'-dimethoxy benzidine, m-xylylene diamine, p-xylyene diamine, 1,3-bis-delta-amino-butyltetramethyl disiloxane, and 1,3-bis-gamma-aminopropyltetraphenyl disiloxane.
Claim 14
Dependent Claim 40 words
The coating medium defined in claim 7 wherein: said diamine is selected from the group consisting of 4,4'-diaminodiphenyl methane, 4,4'-diaminodiphenyl ether, and 1,3-diamino benzene, and said dianhydride is selected from the group consisting of 3,3',4,4'-benzophenonetetracarboxylic dianhydride and 4,4'-(2-acetoxy-1,3-glyceryl) bis-anhydro trimellitate.
Claim 15
Dependent Claim 162 words
A heat curable coating material as defined in claim 1 wherein said aromatic diamine is selected from the group consisting of diamine having the general formula: H.sub.2 N--R'-NH.sub.2 wherein R' is a divalent radical selected from the group consisting of ##STR12## wherein R'" and R"" are an alkyl or an aryl group having 1 to 6 carbon atoms, n is an integer of from 1 to 4 and m has a value of 0, 1 or more and ##STR13## wherein R" is selected from the group consisting of an alkylene chain having 1-3 carbon atoms, ##STR14## wherein R'" and R"" are as above-defined and x is an integer of at least 0; and said aromatic dianhydride is selected from the group consisting of dianhydrides having the general formula: ##STR15## where R is a tetravalent radical containing two benzene rings joined by a non-aromatic non-cyclic group, each pair of carboxyl groups being attached to different adjacent carbon atoms of a single separate ring.
Claim 16
Dependent Claim 49 words
A heat curable coating material as defined in claim 1 wherein said aromatic diamine is selected from the group consisting of 4,4'-diaminodiphenyl ether, and 1,3-diamino benzene and mixtures thereof, and said aromatic dianhydride is selected from the group consisting of 3,3', 4,4'-benzophenonetetracarboxylic dianhydride and 4,4'-(2-acetoxy-1,3-glyceryl)bis-anhydro trimellitate and mixtures thereof.
Claim 17
Dependent Claim 20 words
The heat curable coating medium as defined in claim 1 wherein said aromatic diamide diacid diamine reaction product is ##STR16##
Claim 18
Dependent Claim 20 words
The heat curable coating medium as defined in claim 1 wherein said aromatic diamide diacid diamine reaction product is ##STR17##

References Cited (Backward Citations)

US3505295A Cited
US3663510A Cited
US3652500A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-07-17 1982-01-16 1982-07-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-07-17 1986-01-16 1986-07-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-07-17 1990-01-16 1990-07-18 $7700.00 Window Closed / Lapsed

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