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US4698396A Expired / Lapsed US ⏱️ 0.0 years remaining

Hardenable synthetic resin mixtures

Assignee: VANITCO & Co KG GmbH
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Filing: 1986-04-28
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Granted: 1987-10-06
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Expires: 2006-04-28
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Abstract

Abstract Coating or printing compositions comprising a non-aromatic organic solvent and, as a binder, a hardenable mixture of synthetic resins, as well as methods for coating or printing using such compositions and coated or printed articles made by such methods.

Inventors

  • 👤 Manfred Drawert
  • 👤 Horst Krase
  • 👤 Hans D. Skoda

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 10:44
CPC Classifications
C; C09; C09D; C09D11/00; C09D11/02; C09D11/10; C09D11/102; C08; C08G; C08G59/00; C08G59/18; C08G59/182; C08L; C08L63/00

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 359 words
A coating or printing composition comprising a non-aromatic solvent or solvent mixture and, as a binder, a hardenable synthetic resin mixture comprising (A) a glycidyl compound having more than one epoxy group per molecule and an epoxy value from 0.4 to 0.7; (B) a solid synthetic resin component having free amino groups which is an adduct formed between (1) an excess of a polyaminoamide in turn formed between (a) a dimeric fatty acid, (b) ethylenediamine, and (c) a diamine which is a member selected from the group consisting of aliphatic diamines having from 3 to 20 carbon atoms, such aliphatic amines wherein the carbon chain is interrupted by at least one oxygen atom to form an oxa-compound, cycloaliphatic diamines having 5 or 6 ring members, and heterocyclic diamines having 5 or 6 ring members, and (2) a glycidyl compound having more than one epoxy group per molecule and an epoxy value from 0.4 to 0.7, in which resin component (B) the ratio of (B)(1)(b) to (B)(1)(c) may range from 0.95:0.05 to 0.5:0.5 and from 0.05 to 0.30 equivalent of amine hydrogen atoms of polyaminoamide (B)(1) have been preadducted by reaction with glycidyl compound (B)(2); and (C) a solid polyamide formed between (1) a dimeric fatty acid, (2) ethylenediamine, and (3) a diamine which is a member selected from the group consisting of aliphatic diamines having from 3 to 20 carbon atoms, such aliphatic amines wherein the carbon chain is interrupted by at least one oxygen atom to form an oxa-compound, cycloaliphatic diamines having 5 or 6 ring members, and heterocyclic diamines having 5 or 6 ring members, and (4) a short chain, linear aliphatic monocarboxylic acid in an amount from 0.4 to 0.8 equivalent, based on the total acid equivalents, in which polyamide (C) the equivalent ratio of (C)(1) to (C)(2) is from 1.0:0 to 0.5:0.5 and substantially equivalent amounts of an acid component comprising compounds (C)(1) and (C)(4) and of a basic component comprising amino compounds (C)(2) and (C)(3) are reacted to form said polyamide (C), in which mixture (A) and (B) are present in substantially equivalent amounts and the weight ratio (A)+(B):(C) is from 9:1 to 1.5:1.
Claim 2
Dependent Claim 359 words
A coating or printing composition comprising a non-aromatic solvent or solvent mixture and, as a binder, a hardenable synthetic resin mixture comprising (A) a glycidyl compound having more than one epoxy group per molecule and an epoxy value from 0.4 to 0.7; (B) a solid synthetic resin component having free amino groups which is an adduct formed between (1) an excess of a polyaminoamide in turn formed between (a) a dimeric fatty acid, (b) ethylenediamine, and (c) a diamine which is a member selected from the group consisting of aliphatic diamines having from 3 to 20 carbon atoms, such aliphatic amines wherein the carbon chain is interrupted by at least one oxygen atom to form an oxa-compound, cycloaliphatic diamines having 5 or 6 ring members, and heterocyclic diamines having 5 or 6 ring members, and (2) a glycidyl compound having more than one epoxy group per molecule and an epoxy value from 0.4 to 0.7, in which resin component (B) the ratio of (B)(1)(b) to (B)(1)(c) may range from 0.95:0.05 to 0.5:0.5 and from 0.05 to 0.30 equivalent of amine hydrogen atoms of polyaminoamide (B)(1) have been preadducted by reaction with glycidyl compound (B)(2); and (C) a solid polyamide formed between (1) a dimeric fatty acid, (2) ethylenediamine, and (3) a diamine which is a member selected from the group consisting of aliphatic diamines having from 3 to 20 carbon atoms, such aliphatic amines wherein the carbon chain is interrupted by at least one oxygen atom to form an oxa-compound, cycloaliphatic diamines having 5 or 6 ring members, and heterocyclic diamines having 5 or 6 ring members, and (4) a short chain, linear aliphatic monocarboxylic acid in an amount from 0.4 to 0.8 equivalent, based on the total acid equivalents, in which polyamide (C) the equivalent ratio of (C)(1) to (C)(2) is from 1.0:0 to 0.5:0.5 and substantially equivalent amounts of an acid component comprising compounds (C)(1) and (C)(4) and of a basic component comprising amino compounds (C)(2) and (C)(3) are reacted to form said polyamide (C), in which mixture (A) and (B) are present in substantially equivalent amounts and the weight ratio (A)+(B):(C) is from 9:1 to 1.5:1.
Claim 3
Dependent Claim 58 words
A composition as in claim 1 wherein said glycidyl compound (A) is a member selected from the group consisting of (1) liquid aromatic glycidyl ethers of bisphenol A and bisphenol F having epoxy values from 0.4 to 0.56 and (2) liquid aliphatic glycidyl ethers of neopentyl glycol, glycerine, hexanediol, and diglycerol having epoxy values from 0.6 to 0.7.
Claim 4
Dependent Claim 22 words
A composition as in claim 1 wherein said polyaminoamide (B)(1) is a solid having an amine number from about 30 to 60.
Claim 5
Dependent Claim 30 words
A composition as in claim 1 wherein said codiamine (B)(1)(c) is a member selected from the group consisting of 1,6-diamino-hexane, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane, 1,2-diaminopropane, 1,6-diamino-2,2,4-(2,4,4)-trimethylhexane, 1,12-diamino-4,9-dioxadodecane, 3(4),8(9)-bis(aminotrimethyl)-tricyclo[5.2.1.0 2 ,6 ]decane, and piperazine.
Claim 6
Dependent Claim 27 words
A composition as in claim 1 wherein from 0.05 to 0.30 equivalent of amine hydrogen atoms of said polyaminoamide (B)(1) are preadducted with said glycidyl ether (B)(2).
Claim 7
Dependent Claim 45 words
A composition as in claim 1 wherein said glycidyl compound (B)(2) is a liquid aromatic glycidyl ether of bisphenol A or bisphenol F having an epoxy value from 0.40 to 0.56 and is present in said composition in an amount from 0.05 to 0.30 equivalent.
Claim 8
Dependent Claim 46 words
A composition as in claim 1 wherein said glycidyl compound (B)(2) is a liquid aliphatic glycidyl ether of neopentyl glycol, glycerine, hexanediol, or diglycerol having an epoxy value from 0.6 to 0.7 and is present in said composition in an amount from 0.05 to 0.25 equivalent.
Claim 9
Dependent Claim 52 words
A composition as in claim 1 wherein said polyamide (C) is a waxlike solid having a ring-and-ball softening point not over 150° C., codiamine (C)(3) is present in said polyamide and is 1,6-diaminohexane, 1,6-diamino-2,2,4(2,4,4)-trimethylhexane, 1,13-diamino-4,10-dioxatridecane, piperazine, N-aminoethylpiperazine, or 1,3-bis(4-piperidyl)propane, and said monocarboxylic acid (C)(4) is acetic acid, propionic acid, or butyric acid.
Claim 10
Dependent Claim 40 words
A method for coating a substrate or printing on said substrate which comprises applying a varnish or printing ink composition as in claim 1 to a surface of said substrate and evaporating the solvent or solvent mixture from said composition.
Claim 11
Dependent Claim 16 words
A substrate having a hardened coating or print thereon made by the method of claim 9.

References Cited (Backward Citations)

US583864A Cited
GB988484A Cited
GB1071427A Cited
DE1494525A1 Cited
US4206097A Cited
EP0004850A2 Cited
EP0047364A1 Cited
US4593056A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-10-05 1991-04-06 1991-10-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-10-05 1995-04-06 1995-10-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-10-05 1999-04-06 1999-10-06 $7700.00 Window Closed / Lapsed

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