US4327200A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Water-dilutable oxazolidine group containing epoxy resin esters, coating compositions prepared therefrom, and their use as cathodically depositable paints
Assignee: Allnex Austria GmbH
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Filing: 1980-10-29
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Granted: 1982-04-27
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Expires: 2000-10-29
Abstract
Abstract Binders water-dilutable upon neutralization with inorganic and/or organic acids comprising the reaction product of (A) resins having at least 2 1,2-epoxy groups per molecule and an epoxy equivalent of at least 160; and (B) a semiester of a dicarboxylic acid and an N-2-hydroxyalkyloxazolidine, and a process for the formation of the binders, is described. The binders have sufficient basic groups for neutralization with acids to provide water dilutability, as well as the functional groups required for crosslinking of the binders. The binders upon stoving provide films with good resistance characteristics and have reduced losses.
Inventors
- 👤 Wolfgang Leitner
- 👤 Georg Pampouchidis
- 👤 Anton Bleikolm
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 02:59
CPC Classifications
C; C09; C09D; C09D5/00; C09D5/44; C09D5/4419; C09D5/4423; C09D5/4426; C08; C08G; C08G59/00; C08G59/14; C08G59/1433; C08G59/1477
Claims Analysis
Total Claims: 26
Claim 1
Independent Claim
133 words
Binders water-dilutable upon partial or total neutralization with inorganic and/or organic acids, comprising the reaction product obtained by heating an epoxy resin having at least 2 1,2-epoxy groups per molecule and an epoxy equivalent of at least 160 with a semiester of an aliphatic, cycloaliphatic, or aromatic dicarboxylic acid and an N-2-hydroxyalkyloxazolidine having the general formula-- ##STR4## wherein R 1 is a saturated or unsaturated aliphatic, cycloaliphatic, or aromatic hydrocarbon radical, R 2 is a straight chain or branched alkylene radical, R 3 is a hydrogen atom or an alkyl radical, and R 4 is a hydrogen atom or an alkyl radical with up to 6 carbon atoms, the quantity of oxazolidine semiester being chosen in order that the epoxy-free final product has a theoretical amine number of at least 35 mg KOH/g.
Claim 2
Dependent Claim
133 words
Binders water-dilutable upon partial or total neutralization with inorganic and/or organic acids, comprising the reaction product obtained by heating an epoxy resin having at least 2 1,2-epoxy groups per molecule and an epoxy equivalent of at least 160 with a semiester of an aliphatic, cycloaliphatic, or aromatic dicarboxylic acid and an N-2-hydroxyalkyloxazolidine having the general formula-- ##STR4## wherein R 1 is a saturated or unsaturated aliphatic, cycloaliphatic, or aromatic hydrocarbon radical, R 2 is a straight chain or branched alkylene radical, R 3 is a hydrogen atom or an alkyl radical, and R 4 is a hydrogen atom or an alkyl radical with up to 6 carbon atoms, the quantity of oxazolidine semiester being chosen in order that the epoxy-free final product has a theoretical amine number of at least 35 mg KOH/g.
Claim 3
Dependent Claim
18 words
The binders of claim 1 wherein the N-2-hydroxyalkyloxazolidine is the reaction product of diethanolamine or diisopropanolamine and formaldehyde.
Claim 4
Dependent Claim
22 words
The binders of claim 1 wherein the reaction temperature for producing the reaction product is at from about 60° to 75° C.
Claim 5
Dependent Claim
31 words
The binders of claim 1 wherein the epoxy groups of the epoxy resin are partially reacted with saturated and/or unsaturated carboxylic acids in addition to the reaction with the oxazolidine semiesters.
Claim 6
Dependent Claim
27 words
The binders of claim 1 wherein the reaction product includes other components for introducing additional crosslinking functionality and/or functionality which will influence film formation and/or film surface.
Claim 7
Dependent Claim
47 words
The binders of claim 5 wherein from 30 to 99.5 mole percent of the epoxy groups are reacted with the oxazolidine semiester; from 0.5 to 70 mole percent with primary and/or secondary amine, and with any remaining epoxy groups being reacted with saturated and/or unsaturated carboxylic acids.
Claim 8
Dependent Claim
22 words
The binders of claim 6 wherein from 40 to 60 mole percent of the epoxy groups are reacted with the oxazolidine semiester.
Claim 9
Dependent Claim
13 words
The binders of claim 6 wherein the primary amines include tertiary amine functionality.
Claim 10
Dependent Claim
17 words
The binders of claim 6 wherein the reaction product utilizes primary monoamines in combination with secondary amines.
Claim 11
Dependent Claim
8 words
Coating compositions containing the binders of claim 1.
Claim 12
Dependent Claim
147 words
Process for producing binders water-dilutable upon partial or total neutralization with inorganic and/or organic acids, based on epoxy resin esters, characterized in that the epoxy groups of a resinlike compound with at least 2 1,2-epoxy groups per molecular and an epoxy equivalent of at least 160 are reacted completely at 60°-75° C., with a semiester of an aliphatic, cycloaliphatic, or aromatic dicarboxylic acid and an N-2-hydroxyalkyloxazolidine having the general formula-- ##STR5## wherein R 1 is a saturated or unsaturated aliphatic, cycloaliphatic, or aromatic hydrocarbon radical, R 2 is a straight chain or branched alkylene radical, R 3 is a hydrogen atom or an alkyl radical, and R 4 is a hydrogen atom or an alkyl radical with up to 6 carbon atoms, the quantity of oxazolidine semiester being chosen in order that the epoxy-free final product has a theoretical amine number of at least 35 mg KOH/g.
Claim 13
Dependent Claim
147 words
Process for producing binders water-dilutable upon partial or total neutralization with inorganic and/or organic acids, based on epoxy resin esters, characterized in that the epoxy groups of a resinlike compound with at least 2 1,2-epoxy groups per molecular and an epoxy equivalent of at least 160 are reacted completely at 60°-75° C., with a semiester of an aliphatic, cycloaliphatic, or aromatic dicarboxylic acid and an N-2-hydroxyalkyloxazolidine having the general formula-- ##STR5## wherein R 1 is a saturated or unsaturated aliphatic, cycloaliphatic, or aromatic hydrocarbon radical, R 2 is a straight chain or branched alkylene radical, R 3 is a hydrogen atom or an alkyl radical, and R 4 is a hydrogen atom or an alkyl radical with up to 6 carbon atoms, the quantity of oxazolidine semiester being chosen in order that the epoxy-free final product has a theoretical amine number of at least 35 mg KOH/g.
Claim 14
Dependent Claim
29 words
Process according to claim 11 further characterized in that the reaction charge includes additional compounds which introduce additional crosslinking functionality and/or functionality which influences film formation and/or film surface.
Claim 15
Dependent Claim
26 words
Process according to claim 11 further characterized in that the epoxy-free final product has a theoretical amine number of from about 50 to 140 mg KOH/g.
Claim 16
Dependent Claim
21 words
Process according to claim 11 further characterized in that the N-2-hydroxyalkyloxazolidine is a reaction product of diethanolamine or diisopropanolamine and formaldehyde.
Claim 17
Dependent Claim
21 words
Process according to claim 11 further characterized in that the epoxy groups are partially reacted with saturated and/or unsaturated carboxylic acids.
Claim 18
Dependent Claim
50 words
Process according to claim 11 further characterized in that from 30 to 99.5 mole percent of the epoxy groups are reacted with the oxazolidine semiester; from 0.5 to 70 mole percent with a primary or secondary amine, and any remaining epoxy groups are reacted with saturated and/or unsaturated carboxylic acids.
Claim 19
Dependent Claim
22 words
Process according to claim 16 further characterized in that 40-60 mole percent of the epoxy groups are reacted with the oxazolidine semiester.
Claim 20
Dependent Claim
18 words
Process according to claim 16 further characterized in that the primary amines include a tertiary amine functional group.
Claim 21
Dependent Claim
18 words
Process according to claim 16 further characterized in that primary monoamines are used in combination with secondary amines.
Claim 22
Dependent Claim
29 words
Process according to claim 16 further characterized in that the reaction of the epoxy compound with the oxazolidine semiester, the carboxylic acid, and the amine compound is effected simultaneously.
Claim 23
Dependent Claim
16 words
Process according to claim 16 further characterized in that the amine is reacted separately and subsequently.
Claim 24
Dependent Claim
35 words
Process according to claim 16 further characterized in that the epoxy groups are reacted with the amine, followed by a simultaneous reaction with a semiester intermediate of a dicarboxylic acid, an N-2-hydroxyalkyloxazolidine, and a hydroxyalkyl(meth)acrylate.
Claim 25
Dependent Claim
58 words
Process according to claim 11 further characterized in that from 30 to 99 mole percent of the epoxy groups are reacted with an oxazolidine semiester; from 1 to 30 mole percent with a semiester of a dicarboxylic acid and a tertiary amine alcohol, and the remaining epoxy groups are reacted with saturated and/or unsaturated mono- and/or dicarboxylic acids.
Claim 26
Dependent Claim
38 words
Process according to claim 23 further characterized in that as the esterifying component for the epoxy groups a combination of oxazolidine semiester, semiesters of dicarboxylic acids and tertiary amine alcohols, aliphatic, cycloaliphatic or aromatic dicarboxylic acids are employed.
References Cited (Backward Citations)
US2951058A
Cited
US3994916A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1985-04-26 | 1985-10-26 | 1986-04-27 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1989-04-26 | 1989-10-26 | 1990-04-27 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1993-04-26 | 1993-10-26 | 1994-04-27 | $7700.00 | Window Closed / Lapsed |