Aqueous polyurethane—vinyl polymer hybrid dispersions

• US 10,239,987 B2
• Filed: 07/24/2015
• Issued: 03/26/2019
• Est. Priority Date: 07/31/2014
• Status: Active Grant

• Current Assignee: ALLNEX AUSTRIA GMBH (Allnex Holding S.a r.l.)
• Original Assignee: ALLNEX AUSTRIA GMBH (Allnex Holding S.a r.l.)
• Inventors: Arzt, Anton, Kuttler, Ulrike
• Primary Examiner(s): Buie-Hatcher, Nicole M.
• Application Number:
  US15/326,115
• Publication Number:
  US 20170218110A1
• Time in Patent Office: 1,341 Days
• CPC Class Codes: B05D 3/007 After-treatment
• CPC Class Codes: C08F 220/14 Methyl esters , e.g. methyl (meth)acrylate
• CPC Class Codes: C08F 220/18 with acrylic or methacrylic acids
• CPC Class Codes: C08F 220/1808 C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
• CPC Class Codes: C08F 220/20 of polyhydric alcohols or phenols , e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
• CPC Class Codes: C08F 220/282 and containing two or more oxygen atoms
• CPC Class Codes: C08F 222/1006 of polyhydric alcohols or polyhydric phenols
• CPC Class Codes: C08F 222/102 of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate
• CPC Class Codes: C08F 283/006 on to polymers provided for in C08G18/00 C08F283/004 takes precedence
• CPC Class Codes: C08G 18/0823 containing carboxylate salt groups or groups forming them
• CPC Class Codes: C08G 18/2835 having less than 5 ether groups
• CPC Class Codes: C08G 18/3228 acyclic
• CPC Class Codes: C08G 18/3275 containing two hydroxy groups
• CPC Class Codes: C08G 18/4288 modified by higher fatty oils or their acids or by resin acids
• CPC Class Codes: C08G 18/4291 prepared from polyester forming components containing monoepoxy compounds C08G18/4266 takes precedence
• CPC Class Codes: C08G 18/6254 Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups
• CPC Class Codes: C08G 18/6659 with compounds of group C08G18/34
• CPC Class Codes: C08G 18/67 Unsaturated compounds having active hydrogen
• CPC Class Codes: C08G 18/724 Combination of aromatic polyisocyanates with (cyclo)aliphatic polyisocyanates
• CPC Class Codes: C08G 18/755 and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
• CPC Class Codes: C08G 18/765 : alpha, alpha, alpha', alpha', -tetraalkylxylylene diisocyanate or homologues substituted on the aromatic ring
• CPC Class Codes: C08G 18/792 : formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
• CPC Class Codes: C08G 18/831 : by oxygen-containing compounds inclusive of carbonic acid halogenides, carboxylic acid halogenides and epoxy halides by aldehydes C08G18/84, by peroxides C08G18/86
• CPC Class Codes: C08L 75/06 : from polyesters
• CPC Class Codes: C09D 151/08 : grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• CPC Class Codes: C09D 175/06 : from polyesters
• CPC Class Codes: C09D 5/002 : Priming paints C09D5/08 takes precedence

Abstract

The invention relates to aqueous polyurethane-vinyl polymer hybrid dispersions comprising, as building blocks, hydrophobically modified hydroxy-functional polyesters A, acids B that have further groups which react with isocyanates under formation of urethanes, ureas, or thiourethanes, compounds G having only one hydroxyl group, and one or more tertiary amino groups, olefinically unsaturated monomers H2 having a polymerisable ethylenic unsaturation and a further functional group which reacts with an isocyanate group under bond formation, olefinically unsaturated monomers H1 having at least one polymerisable ethylenic unsaturation and no further functional group which reacts with an isocyanate group, and multifunctional isocyanates I having at least two isocyanate groups per molecule, to a process of their preparation, and to a method of use thereof.

Claims

1. A process for the preparation of an aqueous polyurethane-vinyl polymer hybrid dispersion, comprising

in step a), producing a polyester A′

having residual hydroxyl and acid groups by a polyesterification process wherein a mixture of aliphatic diols A1 and aliphatic and/or aromatic diacids A2, optionally in the presence of hydroxyacids A3, and further optionally, in the presence of one or more of hydroxy compounds A11 having more than two hydroxyl groups, acid compounds A21 having more than two acid groups, or hydroxyacids A31 having more than one hydroxyl group or more than one acid group, or at least two hydroxyl groups and at least two acid groups, is esterified at an elevated temperature of up to 250°

C., under removal of a water formed in the polycondensation reaction,

in step b), producing hydrophobically modified polyesters A by reacting the acid groups of the polyester A′

with a mono-functional compound A4 having an epoxide or aziridine functionality, and a linear or branched alkyl residue of at least four carbon atoms, in which reaction at least 90% of the remaining acid groups are converted to ester or amide groups,

in step c), mixing the hydrophobically modified polyesters A with

acids B that have further groups which react with isocyanates under formation of urethanes, ureas, or thiourethanes,

optionally, hydroxy-functional oligomeric or polymeric compounds C selected from the group consisting of polyesters, polycarbonates, polyethers, polyamides, polydienes and polyenes, and which have at least two hydroxyl groups per molecule, and

optionally, monomeric hydroxy compounds D having at least two hydroxyl groups per molecule,

wherein none, either, or both of C and D are added to the mixture, and

heating the resulting mixture under stirring to at least 60°

C. to form a homogeneous solution,

in step d), adding a substoichiometric quantity of a multifunctional isocyanate I to the homogeneous solution and keeping the reaction temperature in a range of from 60°

C. to 150°

C., to form a prepolymer, and wherein the amount of substance of isocyanate groups in the quantity of multifunctional isocyanate I added is less than the sum of the amounts of substance of isocyanate-reactive hydroxyl groups, of the compounds A, B, C, and D present in this reaction, so that no more unreacted isocyanate groups are present in the reaction mixture,

in step e), adding to this the prepolymer,

a solution which comprises at least one olefinically unsaturated monomer H1 having no further functional group other than one or more vinyl or polymerisable olefinically unsaturated groups, and at least one olefinically unsaturated monomer H2 having at least one hydroxyl group and a vinyl or polymerisable olefinically unsaturated group,

optionally, an antioxydant or radical scavenger, and

optionally, a solvent S which is inert in the reaction, and

homogenising the solution and the prepolymer to form a homogenous mixture,

in step f), adding to the homogeneous mixture, a further multifunctional isocyanate I in stoichiometric excess so that the ratio of the amount of substance of isocyanate groups n(NCO) to the sum n(OH, Σ

) of the amounts of substance of isocyanate-reactive groups hydroxyl groups present in the reaction mixture satisfies the following formula;

n(NCO)/n(OH,Σ

)≥

1.02 mol/mol,

in step g), adding thereto a mixture which comprises compounds G, water, optionally, compounds E, optionally, compounds F,

and homogenising well the resulting mixture,

in step h), adding an aqueous solution of a radical initiator to the mixture of resulting from step g),

and

in step i), polymerising the reaction mixture to obtain a dispersion which is finally cooled to room temperature and filtered.

2. The process of claim 1 wherein in step a), a mixture of aliphatic diols A1 and aliphatic and/or aromatic diacids A2, is esterified at the elevated temperature of up to 250°

C., under removal of the water formed in the polycondensation reaction, and in step b), the polyester A′

formed in the step a) is treated at a temperature of from 150°

C. to 220°

C. with a compound A4 selected from the group consisting of a monoepoxide compound and a monoaziridine compound, whereby the acid groups of the polyester A′

are consumed under addition and formation of an ester or an amide group, and of a hydroxyl or amino group by ring opening of the oxirane or aziridine ring.

3. The process of claim 1 wherein the hydroxy-functional monomers H2 have two hydroxyl groups and are partial esters of polyhydric alcohols having at least two hydroxyl groups, and olefinically unsaturated carboxylic acids selected from the group consisting of acrylic acid, methacrylic acid, and their homologues.

4. The process of claim 1 wherein compounds E and/or compounds F are used.

5. The process of claim 4 wherein compounds E are used, and are selected from the group consisting of the monohydroxymonoamines 2-aminoethanol, 2-methylaminoethanol, and 3-aminopropanol, the dihydroxymonoamines 2-amino-1,3-propanediol, diethanolamine, and 1,1′

-iminodi-2-propanol.

6. The process of claim 1 wherein compounds C and/or compounds D are used.

7. The process of claim 1 wherein a hydroperoxide is used as the radical initiator, and is combined with a reducing agent.