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US5208282A Expired / Lapsed US ⏱️ 0.0 years remaining

Aqueous synthetic resin formulations

Assignee: BASF SE
•
Filing: 1991-05-13
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Granted: 1993-05-04
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Expires: 2011-05-13
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Abstract

Abstract Aqueous synthetic resin formulations containing A) from 3 to 75% by weight of one or more synthetic resins, B) one or more organic compounds having two or more hydrazide groups, C) from 0 to 10% by weight, based on the synthetic resin A, of benzophenone or acetophenone or of one or more acetophenone or benzophenone derivatives which are not monoethylenically unsaturated or of a mixture of these active ingredients, D) effective amounts of emulsifiers or protective colloids or of a mixture of these active ingredients, E) not less than 5% by weight of water and F) from 0 to 85% by weight of finely divided fillers, with the proviso that the total amount of the monomers d polymerized in the one or more synthetic resins A and of component C is from 0.05 to 10% by weight, based on the one or more synthetic resins A, and the ratio of the number of moles of hydrazide groups of component B and the number of moles of the aldehyde and keto groups of the monomers c polymerized in the one or more synthetic resins A is from 0.01 to 2. These synthetic resin formulations are suitable for coating, adhesive bonding, sealing or impregnating.

Inventors

  • 👤 Gerd Rehmer
  • 👤 Maria G. Rau
  • 👤 Eckehardt Wistuba
  • 👤 Reinhard Baecher
  • 👤 Helmut Teichmann
  • 👤 Wilhelm F. Beckerle

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 09:30
CPC Classifications
C; C09; C09D; C09D133/00; C09D133/04; C09D133/06; C09D133/062; C09D133/064; C08; C08K; C08K5/00; C08K5/04; C08K5/07; C08K5/16; C08K5/22; C08K5/24; C08K5/25

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 421 words
An aqueous synthetic resin formulation containing A) from 3 to 75% by weight of one or more synthetic resins which consists of a) from 50 to 99.85% by weight of one or more esters of α, β-monoethylenically unsaturated carboxylic acids of 3 to 6 carbon atoms and alkanols of 1 to 18 carbon atoms or one or more vinyl esters of an aliphatic monocarboxylic acid of 2 to 8 carbon atoms or of a mixture of these monomers (monomer a), b) from 0.1 to 12% by weight of one or more α, β-monoethylenically unsaturated mono- or dibasic acids of 3 to 8 carbon atoms, of anhydrides thereof or of a mixture of these monomers (monomer b), c) from 0.05 to 10% by weight of one or more monoethylenically unsaturated monomers of 2 to 24 carbon atoms which are not an acetophenone or benzophenone derivative and have one or more aldehyde or keto groups or a mixture of both groups (monomer c), d) from 0 to 10% by weight of one or more monoethylenically unsaturated acetophenone or benzophenone derivatives or a mixture of these monomers (monomer d) and e) from 0 to 35% by weight of one or more copolymerizable monoethylenically unsaturated monomers other than monomers (a)-(d) (monomer e), in polymerized form, the percentages by weight of monomers a, b, c and e being chosen within the stated limits so that a synthetic resin consisting only of these monomers would have a glass transition temperature of from 40° to -50° C., B) one or more organic compounds having two or more hydrazide groups, C) from 0 to 10% by weight, based on the synthetic resin A, of benzophenone or acetophenone or of one or more acetophenone or benzophenone derivatives which are not monoethylenically unsaturated or of a mixture of these active ingredients, D) effective amounts of emulsifiers or protective colloids or of a mixture of these active ingredients, E) not less than 5% by weight of water and F) from 0 to 85% by weight of finely divided fillers, with the proviso that the total amount of the monomers d polymerized in the one or more synthetic resins A and of component C is from 0.05 to 10% by weight, based on the one or more synthetic resins A, and the ratio of the number of moles of hydrazide groups of component B and the number of moles of the aldehyde and keto groups of the monomers c polymerized in the one or more synthetic resins A is from 0.01 to 2.
Claim 2
Dependent Claim 421 words
An aqueous synthetic resin formulation containing A) from 3 to 75% by weight of one or more synthetic resins which consists of a) from 50 to 99.85% by weight of one or more esters of α, β-monoethylenically unsaturated carboxylic acids of 3 to 6 carbon atoms and alkanols of 1 to 18 carbon atoms or one or more vinyl esters of an aliphatic monocarboxylic acid of 2 to 8 carbon atoms or of a mixture of these monomers (monomer a), b) from 0.1 to 12% by weight of one or more α, β-monoethylenically unsaturated mono- or dibasic acids of 3 to 8 carbon atoms, of anhydrides thereof or of a mixture of these monomers (monomer b), c) from 0.05 to 10% by weight of one or more monoethylenically unsaturated monomers of 2 to 24 carbon atoms which are not an acetophenone or benzophenone derivative and have one or more aldehyde or keto groups or a mixture of both groups (monomer c), d) from 0 to 10% by weight of one or more monoethylenically unsaturated acetophenone or benzophenone derivatives or a mixture of these monomers (monomer d) and e) from 0 to 35% by weight of one or more copolymerizable monoethylenically unsaturated monomers other than monomers (a)-(d) (monomer e), in polymerized form, the percentages by weight of monomers a, b, c and e being chosen within the stated limits so that a synthetic resin consisting only of these monomers would have a glass transition temperature of from 40° to -50° C., B) one or more organic compounds having two or more hydrazide groups, C) from 0 to 10% by weight, based on the synthetic resin A, of benzophenone or acetophenone or of one or more acetophenone or benzophenone derivatives which are not monoethylenically unsaturated or of a mixture of these active ingredients, D) effective amounts of emulsifiers or protective colloids or of a mixture of these active ingredients, E) not less than 5% by weight of water and F) from 0 to 85% by weight of finely divided fillers, with the proviso that the total amount of the monomers d polymerized in the one or more synthetic resins A and of component C is from 0.05 to 10% by weight, based on the one or more synthetic resins A, and the ratio of the number of moles of hydrazide groups of component B and the number of moles of the aldehyde and keto groups of the monomers c polymerized in the one or more synthetic resins A is from 0.01 to 2.
Claim 3
Dependent Claim 31 words
A synthetic resin formulation as claimed in claim 1, whose synthetic resins A contain, as polymerized monomers, α, β-monoethylenically unsaturated mono- or dicarboxylic acids, anhydrides thereof or mixtures of these monomers.
Claim 4
Dependent Claim 27 words
A synthetic resin formulation as claimed in claim 1, whose synthetic resins A contain, as polymerized monomers c, one or both of the monomers diacetoneacrylamide and diacetonemethacrylamide.
Claim 5
Dependent Claim 34 words
A synthetic resin formulation as claimed in claim 1, whose synthetic resins A contain, as polymerized monomers d, one or more of the compounds ##STR29## where R 3 is --H or --CH 3 .
Claim 6
Dependent Claim 50 words
A synthetic resin formulation as claimed in claim 1, whose synthetic resins A contain the monomers a, b, c and e polymerized in amounts such that a synthetic resin consisting only of the monomers a, b, c and e would have a glass transition temperature of -30° to -10° C.
Claim 7
Dependent Claim 23 words
A synthetic resin formulation as claimed in claim 1, which contains adipic dihydrazide as the organic compound having two or more hydrazide groups.
Claim 8
Dependent Claim 15 words
A synthetic resin formulation as claimed in claim 1, which contains benzophenone as component C.
Claim 9
Dependent Claim 53 words
A synthetic resin formulation as claimed in claim 1, which contains, as component D, a compound of the formula XII ##STR30## where Z is from 1 to 200 and R 37 is --CH 3 or --C 6 H 5 which is substituted by straight-chain or branched alkyl of 1 to 18 carbon atoms.

References Cited (Backward Citations)

GB1193412A Cited
US4246154A Cited
US4267091A Cited
US4435489A Cited
US4927891A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1996-05-03 1996-11-02 1997-05-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2000-05-03 2000-11-02 2001-05-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2004-05-03 2004-11-02 2005-05-04 $7700.00 Window Closed / Lapsed

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