CA2257283A1 - Two-component waterborne polyurethane coating - Google Patents
Two-component waterborne polyurethane coating Download PDFInfo
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- CA2257283A1 CA2257283A1 CA002257283A CA2257283A CA2257283A1 CA 2257283 A1 CA2257283 A1 CA 2257283A1 CA 002257283 A CA002257283 A CA 002257283A CA 2257283 A CA2257283 A CA 2257283A CA 2257283 A1 CA2257283 A1 CA 2257283A1
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- diisocyanate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/20—Diluents or solvents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
Abstract
Disclosed is a two-component aqueous polyurethane coating composition that is curable at 25 degrees Centigrade into a coating exhibiting enhanced hardness, gloss, and solvent resistance. The coating composition comprises a hydroxyl terminated, water dispersible polymer resin and a polyisocyanate which is dispersible in an aqueous polymer resin dispersion, and has an average functionality of at least 2Ø
Description
CA 022~7283 l998-ll-30 Thi~ invention relates generally to two component aqueous polyurethane disper~ions that~have a reduced solvent content. More particularly, thi~
invention relates to two component aqueous polyurethane dispersions, containing low viscosity polyisocyanates, that can be cured at ambient temperature, or, if desired, at higher temperature.
The coatings prepared therefrom have improved hardness, glos~ and solvent resistance compared to conventional aqueous polyurethane dispersions.
One component or two component solvent based polyurethane compositions have been known for many years to produce high guality coatings. However, due to the increasingly strict regulations on the allowable amount of volatile organic compounds emitted during the application of coatings, water based polyurethane have become very important in recent years.
One comron~nt aqueou~ polyurethane dispersions are well known and are used in the production of a variety of useful polyurethane products, including, for example, coatings, adhesives, sealants, and the like. Such dispersions are typically produced by dispersing a water-dispersable, isocyanate-terminated polyurethane prepolymer in an a~ueousmedium together with an active hydrogen contA;n;n~
chain-extender.
The prepolymers used in the preparation of these one component dispersions are generally substantially linear, that is to say difunctional, and are typically obtA;ne~ by reacting an excess of a diisocyanate with an isocyanate-reactive component comprising a polymeric diol in the presence of a reactive compound, for example a diol, contA;n;ng an CA 022~7283 1998-ll-30 ionic or non-ionic hydrophilic group or site.
Even though the one component water based polyurethane dispersions have reduced amounts of organic solvent relative to comparable solvent-based coating compositions, for many applications, they do not exhibit similar coating performance similar to solvent based coating compositions, especially with respect to the properties of gloss, hardness and solvent resistance. This difference is mainly attributable to the lack of chemical crogsl; nk; n~
during the formation of films using the one component, water based systems.
Solvent based two component polyurethane compositions achieve the desired chemical crossl;nk;ng by using multifunctional polyisocyanates, such as those cont~; n; ng isocyanurate groups. Multi-functional polyisocyanates have high viscosities and are hydrophobic in nature. They cannot be dispersed in aqueous dispersions, and hence are unsuitable for water based polyurethane compositions.
Previous attempts to carry out the crossl; nk; ng of two-component aqueous polyurethane dispersions using hydrophilic polyisocyanates have been reported, as described, for example, in U.S. Patent 5,200,4B9 and 5,252,696. These patents di~closed the preparation of a water dispersable polyisocyanate, employing an internal emulsifier, that can be u~ed to prepare two comro~ent polyurethane compositions. However, this internal emulsifier renders the coating resulting from the polyisocyanates sensitive to water. Among the disadvantages of such prior art two-component water CA 022~7283 1998-11-30 based polyurethane coating compositions, prepared using water dispersable polyisocyanates, are a shorter pot life, a higher amount of needed isocyanate crosslinker, and a lower gloss (if the amount of co-solvent is not increased) than otherwise might be desired.
Accordingly, there is a need in the polyurethane coatings industry for no solvent, and low solvent, water-based polyurethane coating lo compositions that provide coating~ characterized by good physical properties, and high gloss and solvent resistance, as compared to solvent-based polyurethane compositions.
In one aspect, the present invention relates to lS a two-component aqueous polyurethane coating composition that iB curable at 25 degrees Centigrade (or at a higher temperature if desired) into a coating exhibiting ~nhAnced hardness, gloss, and solvent resistance, said coating composition comprising:
(I) a polyisocyanate which is dispersible in an a~ueous polymer resin dispersion, has an average functionality of at least 2.0 and contains:
(A) 25% to 95% ~y weight of a polyisocyanate adduct selected from the group consisting of cyclodimers or allorhAnAtes of 3,3,5-_ trimethylhexamethylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-h~A~thylene diisocyanate, and combinationsthereof, and (B) 5% to 75% by weight of another polyisocyanate adduct selected from the group CA 022~7283 1998-ll-30 W O 97/4~475 PCTrUS97/06251 consisting of cyclotrimers or biurets of 3,3,5-trimethylh~Am~thylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinationsthereof, and, (C) 0% to 30~ (preferably 0~ to 20~) by weight of an organic solvent that is inert to isocyanate;
and, (II) an isocyanate reactive hydroxyl-terminated, water dispersable polymer resin having a hydroxyl number of between 10 and 450 (preferably between 28 and 350), with the proviso that if component (B) cons ists essentially of cyclotrimerized isophorone diisocyanate, then component (C) i8 present in an amount of at least 10% by weight, based upon the weight of said coating composition.
In other a6pects, the present invention relates to a process for preparing the above-described coating composition, and to a coated substrate contA;n;ng a coating prepared from the coating composition. The process comprises contacting component (I) and co~ro~Pnt (II) of said two-component aqueous polyurethane coating composition to provide a mixture, and A~ ;ng said mixture to provide a mixed coating composition. The coated substrate is prepared by contacting a substrate with the mixed coating composition.
These and other aspects will become apparent upon reA~ng the following detailed de~cription of the invention.
It has now been surprisingly found, in accordance with the present invention, that /
CA 022~7283 1998-11-30 W O 97/45475 PCTrUS97/06251 combinations of a select group of water-dispersable polyisocyanate adducts enable the preparation of no solvent lor very low solvent) two-compo~ent, coating compositions characterized by good physical properties. These physical properties are comparable to the physical properties only achievable heretofore using high solvent-based, two-component polyurethane coating compositions.
Moreover, coatings on a substrate made in accordance with the present invention have been found to be "mar-resistant" over a wide range of pencil lead hardnesse6, and the coatings tend to exhibit a n self-healing" characteristic inasmuch as scratches in the coating tend to disappear upon standing at room temperature. Thus, the "mar" in the coating caused by a pencil lead scratch is no longer observable after a short period of time. These surprising mar-resistance and self-healing characteristics would provide a commercial advantage in top-coat and clear-coat application~, for example, in automotive coatings.
In the preparation of the coating compositions of the present invention, suitable polyisocyanate adducts are specified,hereinabove. The cyclodimerized polyisocyanate~ cont~;n uretdione moieties and are commonly referred to as "dimers~, whereas the cyclotrimerized polyisocyanates contain isocyanurate moieties and are commonly referred to as "trimersn. The allophanates useful in this invention are suitably made by reacting an alcohol with the designated polyisocyanate to form a c~rhAm~te intermediate, which then further reacts with additional polyisocyanate to form the desired ._ S
CA 022~7283 1998-ll-30 W O 97t45475 PCT~US97/06251 allophanate. Methodology for forming allophanateR
is disclosed, for example, in U.S. Patent Nos.
5,461,135 and 5,124,427.
Other polyisocyanate adducts are suitably additionally employed in the coating compositions of the present invention. Suitable additional polyisocyanate adducts include isocyanurates, allophanate, uretidione or biurets prepared from organic diisocyanates represented by the formula:
R(NCO)2 wherein the R repre~ents an organic group ha~ing a molecular weight of 24 to 2100, preferably 56 to 1000. Preferred diisocyanates according to this invention are those represented by the above formula wherein R represents a divalent aliphatic hydrocarbon group having from 4 to 2S carbons, a divalent cycloaliphatic hydrocarbon group having from 4 to 20 carbons, or a divalent araliphatic hydrocArhQ~ group having from 6 to 20 carbons.
Examples of the organic dii~ocyanates which are particularly suitable for the process include 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 2,2,4-trimethyl-1,6-hexamethylene diisocyanate, 1,10-decanemethylene diisocyanate, 1,12-dodecanemethylene diisocyanate, cyclohPYA~e-1,3-diisocyanate, cyclohPYAne-1,4-dii~ocyanate, 1, _ isocyanato-2-isocyanatomethyl cyclopentane, isophorone diisocyanate, bi8- (4-isocyanatocycloheYyl)-methane, 1,3- and/or 1,4 -bis-(isocyanatomethyl) -cyclohPyAner bi8- (4-isocyanato-3-methyl-cyclohexyl)-methane, ~ '-tetramethyl, 1,3-and/or 1,4-xylene diisocyanate,1-isocyanato-1-methyl-4(3)-isocyanatomethyl cyclo~eY~ne, 2,4-and/or CA 022~7283 1998-11-30 W 097/45475 PCT~US97106251 2,6-hexahydrotolylene diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, m- and p-tetramethylxylene diisocyanates, p-xylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,4~-diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanates, 5-naphthalene diisocyanate. Mixtures of polyisocyanates can also be used and also polyisocyanates which have been modified by the introduction of urethane, allophanate, urea, biuret, carbodiimide, ureton; mi n~
or isocyanurate residues.
The organic solvent optionally employed in the coating compositions of the present invention are is suitably a solvent that does not contain isocyanate reactive groups. Examples of suitable solvents are acetone, methylamyl ketone, methylethyl ketone, methyisobutyl ketone, n-methylpyrrolidone, dimethylformamide, dimethylacetamide, n-butylacetate, dipropylene glycol dimethyl ether, propylene glycol methylethylacetate, propylene glycol methylether, and other such water-compatible solvents. Mixtures o~ the solvents may also be u~ed.
The isocyanate reactive hydroxyl terminated aqueous dispersable resin polymer employed in the coating composition of the present invention suitably has a hydroxyl n-lmh~r of between 10 to 450.
Preferably, the hydroxyl number is between 28 to 350. Illustrative hydroxyl-terminated polymers are represented by the formula:
CA 022~7283 1998-11-30 W O 97145475 PCT~US97/06251 Rl(OH)n wherein Rl represents (a) a polyester, or (b) a polyether, or (c) a polyurethane, or (d) a polyacrylate, or (e) a copoly(urethane-acrylate), or a combination thereof, ha~ing a molecular weight between 200 to 8,000, preferably between 230 to 6,000. The functionality of the hydroxyl terminated polymer represented in the formula by n can be between 1.8 and 8, preferably between 2 and 6.
The hydroxyl-terminated, water disper6ible polymer resin according to this invention also has 1% to 20% by weight of non-ionic and/or ionic hydrophilic groups, preferably between 2 to 10~.
The suitable non-ionic groups are polymeric ethylene oxides with 3 to 30 repeating ethylene oxide units.
The suitable ionic groups are carboxylic, sulfonic, sulfate and ~uaternary ammonium groups.
Specific examples of the polyesters are the reaction products of one or more kinds of polycarboxylic acids such as saturated aliphatic carboxylic acids, and/or aromatic carboxylic acid and one or more kinds of polyhydric alcohols.
Examples of aliphatic,acids are oxalic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, sebacic acid, isosebacic acid, and azelaic acid. Examples of aromatic acids are phthalic acid, isophthalic acid, terephthAlic acid and their anhydrides. Examples of the polyhydric - - alcohols are ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, diethylene glycol, triethylene glycol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 1,5-pentanediol, 1,4-pentanediol, 1,6-CA 022~7283 l998-ll-30 W O 97/4547S PCT~US97/06251 he~An~diol, 1,5-he~nediol, 1,4-he~An~diol, 1,3-hexanediol, 2,3-hexAnediol, 2,4-he~Ane~;ol, 2,5-he~Anediol, 8~4-he~Anediol~ 1,7-heptanediol, 1,6-heptanediol, 1,5-heptanediol, 1,4-heptanediol, 1,3-heptanediol, 2,3-heptanediol, 2,4-heptanediol, 2,5-heptanediol, neopentyl glycol, 2,2-diethyl-1,3-propanediol, 2-ethyl-2-butyl-1,3-propanediol, 1,4-cyclohe~nedimethanol, trimethylolpropane, and glycerol. The polyesters in according to this invention have molecular weight range between 150 to 8,000, preferably between 450 to 4,000. They have functionality between 1.5 to 8, preferably between 1.8 to 4.
Specific examples of the polyethers are the polymers obtained by the reaction of starting compounds which contain reactive hydrogen atoms with al~ylene oxides such a~ propylene oxide, butylene oxide, styrene oxide, tetrahydrofuran, epichlorohydrin or mixture6 of these alkylene oxides. Certain proportions of ethylene oxide may also be included. Suitable starting compounds cont~;n;n~ at least one reactive hydrogen atom include the polyols set forth as suitable for preparing the polyhyd~oxy polyesters and, in addition, water, methanol, ethanol, 1,2,6-he~netriol, 1,2,4-butanetriol, trimethylol ethane, pentaerythritol, mannitol, sorbitol, methyl glycoside, sucrose, phenol, isononyl phenol, resorcinol, hydro~linone and 1,1,1- or 1,1,2-~0 tris(hydroxylphenyl)ethane. The polyethers inaccording to this invention have molecular weight between 150 to 8,000, preferably between 200 to 6,000. They have functionality between 1.5 to 8.
.. . . . . . . . . . . . . . . . . ..
CA 022~7283 1998-ll-30 Preferably between 1.8 to 4.
Specific examples of the polyurethanes are the reaction product~ of a diisocyanate and a polyol.
The diisocyanates suitable for this invention are organic diisocyanates represented by the formula:
R(NC0) 2 wherein the R represents an organic group having a molecular weight of 24 to 2100, preferably 56 to 1000. Preferred diisocyanates according to this invention are tho~e represented by the above formula wherein R represents a divalent aliphatic hydrocarbon group having from 4 to 25 cArho~R, a divalent cycloaliphatic hydrocarbon group having from 4 to 20 carbons, or a divalent araliphatic hydrocarbon group having from 6 to 20 carbons.
Examples of the organic diisocyanate~ which are particularly suitable for the proces~ include ethylene diisocyanate, 1,4-tetramethylene dii~ocyanate, 1,6-hexamethylene diisocyanate, 2,2,4-trimethyl-1,6-hexamethylene diisocyanate, 1,10-decanemethylene diisocyanate, 1,12-dodecanemethylene diisocyanate, cycloheYAne-1,3-diisocyanate, cycloheYAne-1,4-diisocyanate, 1, isocyanato-2-isocyanatomethyl cycl,opentane, isophorone diisocyanate, bis-(4-isocyanatocyclohexyl)-methane, 1,3- and/or 1,4-bis-(isocyanatomethyl)-cyclohPYAne, bis-(4-isocyanato-3-methyl-cyclohexyl)-methane, ~,a,~',a'-tetramethyl, 1,3-and/or 1,4-xylene diisocyanate,l-i~ocyanato-l-methyl-4(3)-isocyanatomethyl cyclohP~YAnP~ 2,4-and/or 2,6-hexahydrotoluylene diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, m- and p-tetramethylxylene diisocyanates, p-xylene /o CA 022~7283 1998-ll-30 diisocyanate, 1,4-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanates, 5-naphthalene diisocyanate. Suitable polyols include those described above as polyesters and polyethers, as well as hydroxyl terminated polylactones, and hydroxyl terminated polycarbonates.
Suitable hydroxyl terminated polylactones are polymeric products of valeratelactone, or ~-caprolactone having molecular weight between 400 and 6000, preferably between 650 and 3,000.
Suitable hydroxyl terminated polycarbonate~ are reaction products obtained from reaction of the polydydric alcohols previously set forth for preparing the polyhydroxyl polyesters with phosgene, diaryl carbonates such diphenyl carbonate or cyclic cArhonAtes such as ethylene or propylene carbonate.
Al~o suitable are polyester cArho~Ates or polyether carbonates obtained by the reaction of lower molecular weight oligomer of the above-mentioned polyesters, polylactones, or polyethers with phosgene, diaryl cArh~nAtes or cyclic carbonates.
The hydroxyl terminated polycarbonates suitable for this invention have molecular weight between 250 to 8,000, preferably between 650 and 3,000.
Specific examples of hydroxyl group-contA;n;ng polyacrylates are the polymers obt A; n~ by polymerization of one or more kind~ of unsaturated hydroxylacrylic monomers (e.g. 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2-hydroxyacrylate), unsaturated acrylic acid amide CA 022~7283 1998-ll-30 W O 97/45475 PCTrUS97/06251 monomer6 (e.g. acrylamide, N-methylolacrylamide, methacrylamide), unsaturated carboxylic acid monomers (e.g. acrylic acid, methacrylic acid, itaconic acid, crotonic acid), unsaturated acid anhydride monomers (e.g. itaconic anhydride, maleic anhydride), unsaturated glycidyl monomers (e.g.
glycidyl acrylate, glycidyl methacrylate), acrylic ester monomers (e.g. ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate), methacrylic ester monomers (e.g. methyl methacrylate, n-lauryl methacrylate, isobutyl methacrylate), maleic ester monomers (e.g. dibutyl maleate, diethyl maleate), fumaric ester monomer6 (e.g. dibutyl fumarate, diethyl fumarate), styrene and its derivatives (e.g.
~-methylstyrene, ~-chloro6tyrene, ~-bromostyrene, p-bromostyrene), nitriles (e.g. acrylonitrile, methylacrylonitrile, ethylacrylonitrile~ and the like.
Specific examples of copoly(urethane-acrylate) are copolymers prepared as described for compo~Pnt (c), except between 2 to 50 percent by weight of component (d) was used a~ the polyol.
The two component coating compositions according to this invention are prepared by m;~;ng of the polyisocyanate, compo~ent (I), into the isocyanate reactive aqueous solution and/or dispersion of hydroxyl terminated polymer, co...~o~ent (II). ~;~r;ng of the two col~ro~nts is suitably carried out by simple stirring or sh~k; ng at room temperature without high energy. The quantity of the polyisocyanate component is selected to provide an NCO/OH equivalent ratio, based on the isocyanate groups of component (I), and the hydroxyl groups of /'~
CA 022~7283 1998-11-30 W 097/45475 PCT~US97/062Sl component (II), of about 1 to 5, preferably about 1.2 to 2Ø The mixtures prepared according to this invention have good pot-life and spray viscosity of more than two hours.
Before polyisocyanate component (I) i8 mixed into isocyanate reactive component (II), the auxiliaries and additives typically used in coating technology may be incorporated into the isocyanate reactive component (II). The auxiliaries and additives include foam inhibitors, leveling aids, pigments, dispersion aids for solid pigments, surface active agents, etc.
The two-component coating compositions according to this invention thus obtained are lS suitable for virtually any applications solvent-cont~in;ng, solventless, or other aqueous paint and coating systems on substrate~ are currently used.
Examples of the applications include the painting and coating of metal surfaces, the painting and coating of plastic surfaces, the painting, coating, or sealing of wood and wood based material~ such as particle board, fiber board and paper, the painting, coating, or sealing of mineral material surfaces such as lime- and/or çement-bound building material and concrete, and the painting and coating of bitumen-cont~;ning pavements. They are also suitable for the ho~ng of various materials wherein the materials of two surfaces may be the same of different.
30- The aqueous coating compositions according to the present invention may be applied to substrates using any of the various techniques known in the art, such as spraying, roll-on, brush-on and 80 on.
....
CA 022~7283 1998-ll-30 W 097/45475 PCT~US97/06251 They can also contain pigments, levelling agents, catalysts, and other auxiliaries known in the art.
The invention i5 further illustrated in, but is not intended to be limited by, the following examples in which all parts and percentages are by weight unless otherwi~e specified.
EXAMPLE 1 - Preparation of a Coating Containing HDI
Dimer Plus HDI Trimer With Solvent.
Step 1 PreParation of Low Vi~cosity HDI Dimer/HDI Trimer Isocyanate Crosslinker The HDI dimer/HDI trimer isocyanate crosslinker was prepared by blen~ing: (a) 100 parts of low viscosity he~methylene diisocyanate (HDI) dimer;
(b) 100 parts of HDI trimer; and (c) 35.29 parts of dipropylene glycol dimethyl ether (commercially available as PROGLYDE DMM, a product of Dow Chemical Company). These materials were stirred for 30 minutes at room temperature.
Step 2 Preparation of the Pol w rethane Ionomer and the Aqueous DisPersion of PolYurethane Resin To an appropriate sized reaction vessel, namely a 3-neck round bottom fla~k, equipped with a stirrer, a temperature control, a co~nRer, and a nitrogen purge, the following five ingredients were charged: (1) polyester polyol in an amount of 110.92 parts (OH eguivalent weight=270.75)~; (2) isophorone /~
CA 022~7283 1998-11-30 W O 97/45475 PCT~US97106251 diisocyanate (IPDI) monomer in an amount of 45.48 part~; (3) dimethylol propionic acid (DMPA) in an amount of 13.60 parts; (4) N-methyl pyrroli~;no~e (NMP) in an amount of 30.OO parts; and, (5) T-12 (dibutlytin dilaurate) catalyst in an amount of 0.10 parts .
This reaction mixture was heated to 80~C and maintained until the NC0 peak was no longer apparent by IR. 185 parts of said ionomer was weighed into an 800mL dispo~able beaker and set aside for preparation of dispersion as follows.
To neutralize the carboxyl concentration in the ionomer, 8.78 parts of dimethylethanolamine (DMEA) was added to a 250mL disposable beaker along with tap water, in an amount of 199.76 parts. This mixture was manually ~tirred into solution with a ~poonula. The io~o~r wa~ placed under moderate agitation using a Premier Mill dispersator equipped with a ~hi-vis" mix head. To this ionomer, the above water/amine solution was charged and dispersed to provide the desired aqueous dispersion of ionomer.
Step 3 PreParation and Te~tinq of Two-ComPonent (2K) PolYurethane-HDI Dimer/HDI Trimer coatinq Crosslinking of the two-component composition was effected by first A~;ng to an eight ounce glass bottle the following ingredients: isocyanate crosslinker (from Step 1 of the present Example) in an amount of 18.17 parts; dispersion of ionomer (from Step 2 of the present Example) in an amount of 66.23 part~; OSi Specialties, Inc.'s SILWET L-7604 .. . . .. . . ..... . . . .
CA 022~7283 1998-11-30 (10% aqueous) in an amount of 0.80 parts; OSi Specialties, Inc.~s SILWET L-7605 (10% aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as Dow Chemical Company's PROGLYDE DMM) in an amount of 12.53 parts; and, water in an amount of 12.40 parts. Standard tests were conducted on the resulting coating, and the results are give in Table 1 below.
The coated test panels were allowed to cure at ambient temperature and humidity conditions for two weeks before testing for appearance, mechanical properties, and chemical resistance. Pencil hardness was determined according to ASTM D3363-92a.
The conical mandrel bend tests were performed using a one-eight inch tester from BYK-Gardner, Inc.
according to ASTM DS22-92. Direct and reverse impact ~alues were determined according to ASTM
D2794-92 using a variable height impact tester from BYR-Gardner, Inc. G1OBB was determined using a micro-TRZ-gloss, multi-angle glossmeter from BYK-Gardner. Cross-hatch adhesion was determined using a cross-hatch cutter from BYK-Gardner according to ASTM D3359-92a. Chemical Resistance was determined according to ASTM D1308-87.
/~
T ~ L~ 1 Physical Pro~ert~ Result Chem. Property Result Thickness (mils) 2.85 CHEMICAL RESISTANCE
Mandrel Bend (1/4n) PASS (10% in water [1/2 hour 20~ Micro-Gloss 84.95 test]) 60~ Micro-Gloss 92.30 Acetic Acid PASS
Impact (direct) ~160 Sodium Hydroxide PASS
Impact (reverse) +160 Hydrochloric Acid PASS
Cross-Hatch PASS SO~VENT RESISTANCE
Max. Pencil Hard. ~9H* (l/2 hour test under 2 n MEK Rub (100 cycles) PASS watch glas~) Xylene PASS
Methyl Ethyl Ketone PASS
* Coating provided "~r-resistance" in 2B-9H Pencil Hardne~s te~t~.
EXAMPLE 2 - Preparation of a Coating Composition Co~tA~ning HDI Dimer P1UB HDI Trimer With No Solvent.
Step 1 PreParation of 100% Solids HDI Dimer/HDI Trimer I~ocYanate Crosslinker To an appropriate reaction vessel, namely a 3-_ neck round bottom fla~k equipped with stirring and a nitrogen purge, the following two ingredients were charged: (1) low viscosity hexamethylene diisocyanate (HDI) dimer in an amount of 35.00 parts; (2) HDI trimer in an amount of 35.00 parts.
These materials were stirred for 30 minutes at room temperature.
/~
CA 02257283 1998-ll-30 W O 97/45475 PCTrUS97/06251 Step 2 Preparation of the Coatinq Com~osition Crossl; nk; n~ followed the procedure as set out in Example 1 above, using ingredient weights that follow: isocyanate crosslinker (see Example 1, Step 1) in an amount of 18.40 parts; dispersion (see Example 1, Step 2) in an amount of 66.23 parts;
SILWET L-7604 (10% aqueous) in an amount of 0.80 parts; SILWET L-7605 (10% aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as PROGLYDE DMM) in an amount of 12.53 parts; and, water in an amount of 12.40 parts, thus forming the desired coating composition having physical and chemical properties as shown in Table 2.
Physical Pro~ertY Result Chem. ProPerty Result Thickness (mils) 2.65 CHEMICAL RESISTANCE
Mandrel Bend (1/4n) PASS (10~ in water [1/2 hour 20~ Micro-Gloss 85.0 te8tl) 60~ Micro-Gloss 81.5 Acetic Acid PASS
Impact (direct) +~60 Sodium Hydroxide PASS
Impact (reverse) +160 Hydrochloric Acid PASS
Cro~s-Hatch PASS SOLVENT RESISTANCE
Max. Pencil Hard. ~9H* (1/2 hour test under 2"
MEK Rub (100 cycles) PASS watch glass) Xylene PASS
Methyl Ethyl Ketone PASS
* Coating provided "mar-resistance" in 2B-9H Pencil Hardness te~t~.
/~
CA 022~7283 l998-ll-30 W O 97/45475 PCTrUS97/06251 EXAMPLE 3 - Preparation of a Coating Composition Cont~;n;ng Allophanate Plus HDI Trimer With No Solvent.
Step 1 Pre~aration of HDI Trimer/AlloPhanate IsocYanate Cro~slinker The following trimer/allophanate variation was prepared using the procedure of Example 1, Step 1, but without solvent:
HDI Trimer 35.00 parts A~OPHANATE 35.00 parts Step 2 PreParation of the Coatinq Com~osition Cros61;nking followed the procedure as set out in Example 1 above, using ingredient weights that follow: isocyanate crosslinker (see Example 1, Step 1) in an amount of 18.86 parts; disper6ion (see Example 1, Step 2) in an amount of 66.23 parts;
SILWET L-7604 (10% aq~eous) in an amount of 0.80 parts; SI~WET ~-7605 (10% aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as PROGLYDE DMM) in an amount of 12.~3 parts; and, water in an amount of 12.40 parts, thus forming the desired coating composition.
.. , . . ~ ~
CA 022~7283 1998-11-30 W 097/45475 PCTrUS97/06251 EXAMPLE 4 - Preparation of a Coating Cont~' ni ng Allophanate P1UB IPDI Trimer.
Step 1 Pre~aration of IPDI Trimer/Allo~hanate IsocYanate Crosslinker The following trimer/allophanate variation was prepared using the procedure of Example 1, Step 1:
IPDI Trimer 35.00 parts ALLOPHANATE 35.00 parts DMM 17.50 parts Step 2 PreParation of the Coatinq Com~osition Crossl; nki ng followed the procedure as set out in Example 1 above, using ingredient weights that follow: isocyanate crosslinker (see Example 1, Step 1) in an amount of 22.88 parts; dispersion (see Example 1, Step 2) in an amount of 66.23 parts;
SILWET L-7604 (10% aqueousJ in an amount of 0.80 parts; SILWET L-7605 l10~ aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as PROGLYDE DMM) in an amount of 12.53 parts; and, water in an amount of 12.40 parts, thus forming the desired coating composition.
While the invention has been described above -with reference to specific embodiments thereof, it iB apparent than many changes, modifications and variations can be made without departing from the inventive concept disclosed herein. Accordingly, it ~1 CA 02257283 1998-ll-30 i8 intended to embrace all such changes, modifications and variations that fall within the spirit and broad scope of the appended claim~.
. , .. ~ .... . .
invention relates to two component aqueous polyurethane dispersions, containing low viscosity polyisocyanates, that can be cured at ambient temperature, or, if desired, at higher temperature.
The coatings prepared therefrom have improved hardness, glos~ and solvent resistance compared to conventional aqueous polyurethane dispersions.
One component or two component solvent based polyurethane compositions have been known for many years to produce high guality coatings. However, due to the increasingly strict regulations on the allowable amount of volatile organic compounds emitted during the application of coatings, water based polyurethane have become very important in recent years.
One comron~nt aqueou~ polyurethane dispersions are well known and are used in the production of a variety of useful polyurethane products, including, for example, coatings, adhesives, sealants, and the like. Such dispersions are typically produced by dispersing a water-dispersable, isocyanate-terminated polyurethane prepolymer in an a~ueousmedium together with an active hydrogen contA;n;n~
chain-extender.
The prepolymers used in the preparation of these one component dispersions are generally substantially linear, that is to say difunctional, and are typically obtA;ne~ by reacting an excess of a diisocyanate with an isocyanate-reactive component comprising a polymeric diol in the presence of a reactive compound, for example a diol, contA;n;ng an CA 022~7283 1998-ll-30 ionic or non-ionic hydrophilic group or site.
Even though the one component water based polyurethane dispersions have reduced amounts of organic solvent relative to comparable solvent-based coating compositions, for many applications, they do not exhibit similar coating performance similar to solvent based coating compositions, especially with respect to the properties of gloss, hardness and solvent resistance. This difference is mainly attributable to the lack of chemical crogsl; nk; n~
during the formation of films using the one component, water based systems.
Solvent based two component polyurethane compositions achieve the desired chemical crossl;nk;ng by using multifunctional polyisocyanates, such as those cont~; n; ng isocyanurate groups. Multi-functional polyisocyanates have high viscosities and are hydrophobic in nature. They cannot be dispersed in aqueous dispersions, and hence are unsuitable for water based polyurethane compositions.
Previous attempts to carry out the crossl; nk; ng of two-component aqueous polyurethane dispersions using hydrophilic polyisocyanates have been reported, as described, for example, in U.S. Patent 5,200,4B9 and 5,252,696. These patents di~closed the preparation of a water dispersable polyisocyanate, employing an internal emulsifier, that can be u~ed to prepare two comro~ent polyurethane compositions. However, this internal emulsifier renders the coating resulting from the polyisocyanates sensitive to water. Among the disadvantages of such prior art two-component water CA 022~7283 1998-11-30 based polyurethane coating compositions, prepared using water dispersable polyisocyanates, are a shorter pot life, a higher amount of needed isocyanate crosslinker, and a lower gloss (if the amount of co-solvent is not increased) than otherwise might be desired.
Accordingly, there is a need in the polyurethane coatings industry for no solvent, and low solvent, water-based polyurethane coating lo compositions that provide coating~ characterized by good physical properties, and high gloss and solvent resistance, as compared to solvent-based polyurethane compositions.
In one aspect, the present invention relates to lS a two-component aqueous polyurethane coating composition that iB curable at 25 degrees Centigrade (or at a higher temperature if desired) into a coating exhibiting ~nhAnced hardness, gloss, and solvent resistance, said coating composition comprising:
(I) a polyisocyanate which is dispersible in an a~ueous polymer resin dispersion, has an average functionality of at least 2.0 and contains:
(A) 25% to 95% ~y weight of a polyisocyanate adduct selected from the group consisting of cyclodimers or allorhAnAtes of 3,3,5-_ trimethylhexamethylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-h~A~thylene diisocyanate, and combinationsthereof, and (B) 5% to 75% by weight of another polyisocyanate adduct selected from the group CA 022~7283 1998-ll-30 W O 97/4~475 PCTrUS97/06251 consisting of cyclotrimers or biurets of 3,3,5-trimethylh~Am~thylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinationsthereof, and, (C) 0% to 30~ (preferably 0~ to 20~) by weight of an organic solvent that is inert to isocyanate;
and, (II) an isocyanate reactive hydroxyl-terminated, water dispersable polymer resin having a hydroxyl number of between 10 and 450 (preferably between 28 and 350), with the proviso that if component (B) cons ists essentially of cyclotrimerized isophorone diisocyanate, then component (C) i8 present in an amount of at least 10% by weight, based upon the weight of said coating composition.
In other a6pects, the present invention relates to a process for preparing the above-described coating composition, and to a coated substrate contA;n;ng a coating prepared from the coating composition. The process comprises contacting component (I) and co~ro~Pnt (II) of said two-component aqueous polyurethane coating composition to provide a mixture, and A~ ;ng said mixture to provide a mixed coating composition. The coated substrate is prepared by contacting a substrate with the mixed coating composition.
These and other aspects will become apparent upon reA~ng the following detailed de~cription of the invention.
It has now been surprisingly found, in accordance with the present invention, that /
CA 022~7283 1998-11-30 W O 97/45475 PCTrUS97/06251 combinations of a select group of water-dispersable polyisocyanate adducts enable the preparation of no solvent lor very low solvent) two-compo~ent, coating compositions characterized by good physical properties. These physical properties are comparable to the physical properties only achievable heretofore using high solvent-based, two-component polyurethane coating compositions.
Moreover, coatings on a substrate made in accordance with the present invention have been found to be "mar-resistant" over a wide range of pencil lead hardnesse6, and the coatings tend to exhibit a n self-healing" characteristic inasmuch as scratches in the coating tend to disappear upon standing at room temperature. Thus, the "mar" in the coating caused by a pencil lead scratch is no longer observable after a short period of time. These surprising mar-resistance and self-healing characteristics would provide a commercial advantage in top-coat and clear-coat application~, for example, in automotive coatings.
In the preparation of the coating compositions of the present invention, suitable polyisocyanate adducts are specified,hereinabove. The cyclodimerized polyisocyanate~ cont~;n uretdione moieties and are commonly referred to as "dimers~, whereas the cyclotrimerized polyisocyanates contain isocyanurate moieties and are commonly referred to as "trimersn. The allophanates useful in this invention are suitably made by reacting an alcohol with the designated polyisocyanate to form a c~rhAm~te intermediate, which then further reacts with additional polyisocyanate to form the desired ._ S
CA 022~7283 1998-ll-30 W O 97t45475 PCT~US97/06251 allophanate. Methodology for forming allophanateR
is disclosed, for example, in U.S. Patent Nos.
5,461,135 and 5,124,427.
Other polyisocyanate adducts are suitably additionally employed in the coating compositions of the present invention. Suitable additional polyisocyanate adducts include isocyanurates, allophanate, uretidione or biurets prepared from organic diisocyanates represented by the formula:
R(NCO)2 wherein the R repre~ents an organic group ha~ing a molecular weight of 24 to 2100, preferably 56 to 1000. Preferred diisocyanates according to this invention are those represented by the above formula wherein R represents a divalent aliphatic hydrocarbon group having from 4 to 2S carbons, a divalent cycloaliphatic hydrocarbon group having from 4 to 20 carbons, or a divalent araliphatic hydrocArhQ~ group having from 6 to 20 carbons.
Examples of the organic dii~ocyanates which are particularly suitable for the process include 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 2,2,4-trimethyl-1,6-hexamethylene diisocyanate, 1,10-decanemethylene diisocyanate, 1,12-dodecanemethylene diisocyanate, cyclohPYA~e-1,3-diisocyanate, cyclohPYAne-1,4-dii~ocyanate, 1, _ isocyanato-2-isocyanatomethyl cyclopentane, isophorone diisocyanate, bi8- (4-isocyanatocycloheYyl)-methane, 1,3- and/or 1,4 -bis-(isocyanatomethyl) -cyclohPyAner bi8- (4-isocyanato-3-methyl-cyclohexyl)-methane, ~ '-tetramethyl, 1,3-and/or 1,4-xylene diisocyanate,1-isocyanato-1-methyl-4(3)-isocyanatomethyl cyclo~eY~ne, 2,4-and/or CA 022~7283 1998-11-30 W 097/45475 PCT~US97106251 2,6-hexahydrotolylene diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, m- and p-tetramethylxylene diisocyanates, p-xylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,4~-diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanates, 5-naphthalene diisocyanate. Mixtures of polyisocyanates can also be used and also polyisocyanates which have been modified by the introduction of urethane, allophanate, urea, biuret, carbodiimide, ureton; mi n~
or isocyanurate residues.
The organic solvent optionally employed in the coating compositions of the present invention are is suitably a solvent that does not contain isocyanate reactive groups. Examples of suitable solvents are acetone, methylamyl ketone, methylethyl ketone, methyisobutyl ketone, n-methylpyrrolidone, dimethylformamide, dimethylacetamide, n-butylacetate, dipropylene glycol dimethyl ether, propylene glycol methylethylacetate, propylene glycol methylether, and other such water-compatible solvents. Mixtures o~ the solvents may also be u~ed.
The isocyanate reactive hydroxyl terminated aqueous dispersable resin polymer employed in the coating composition of the present invention suitably has a hydroxyl n-lmh~r of between 10 to 450.
Preferably, the hydroxyl number is between 28 to 350. Illustrative hydroxyl-terminated polymers are represented by the formula:
CA 022~7283 1998-11-30 W O 97145475 PCT~US97/06251 Rl(OH)n wherein Rl represents (a) a polyester, or (b) a polyether, or (c) a polyurethane, or (d) a polyacrylate, or (e) a copoly(urethane-acrylate), or a combination thereof, ha~ing a molecular weight between 200 to 8,000, preferably between 230 to 6,000. The functionality of the hydroxyl terminated polymer represented in the formula by n can be between 1.8 and 8, preferably between 2 and 6.
The hydroxyl-terminated, water disper6ible polymer resin according to this invention also has 1% to 20% by weight of non-ionic and/or ionic hydrophilic groups, preferably between 2 to 10~.
The suitable non-ionic groups are polymeric ethylene oxides with 3 to 30 repeating ethylene oxide units.
The suitable ionic groups are carboxylic, sulfonic, sulfate and ~uaternary ammonium groups.
Specific examples of the polyesters are the reaction products of one or more kinds of polycarboxylic acids such as saturated aliphatic carboxylic acids, and/or aromatic carboxylic acid and one or more kinds of polyhydric alcohols.
Examples of aliphatic,acids are oxalic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, sebacic acid, isosebacic acid, and azelaic acid. Examples of aromatic acids are phthalic acid, isophthalic acid, terephthAlic acid and their anhydrides. Examples of the polyhydric - - alcohols are ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, diethylene glycol, triethylene glycol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 1,5-pentanediol, 1,4-pentanediol, 1,6-CA 022~7283 l998-ll-30 W O 97/4547S PCT~US97/06251 he~An~diol, 1,5-he~nediol, 1,4-he~An~diol, 1,3-hexanediol, 2,3-hexAnediol, 2,4-he~Ane~;ol, 2,5-he~Anediol, 8~4-he~Anediol~ 1,7-heptanediol, 1,6-heptanediol, 1,5-heptanediol, 1,4-heptanediol, 1,3-heptanediol, 2,3-heptanediol, 2,4-heptanediol, 2,5-heptanediol, neopentyl glycol, 2,2-diethyl-1,3-propanediol, 2-ethyl-2-butyl-1,3-propanediol, 1,4-cyclohe~nedimethanol, trimethylolpropane, and glycerol. The polyesters in according to this invention have molecular weight range between 150 to 8,000, preferably between 450 to 4,000. They have functionality between 1.5 to 8, preferably between 1.8 to 4.
Specific examples of the polyethers are the polymers obtained by the reaction of starting compounds which contain reactive hydrogen atoms with al~ylene oxides such a~ propylene oxide, butylene oxide, styrene oxide, tetrahydrofuran, epichlorohydrin or mixture6 of these alkylene oxides. Certain proportions of ethylene oxide may also be included. Suitable starting compounds cont~;n;n~ at least one reactive hydrogen atom include the polyols set forth as suitable for preparing the polyhyd~oxy polyesters and, in addition, water, methanol, ethanol, 1,2,6-he~netriol, 1,2,4-butanetriol, trimethylol ethane, pentaerythritol, mannitol, sorbitol, methyl glycoside, sucrose, phenol, isononyl phenol, resorcinol, hydro~linone and 1,1,1- or 1,1,2-~0 tris(hydroxylphenyl)ethane. The polyethers inaccording to this invention have molecular weight between 150 to 8,000, preferably between 200 to 6,000. They have functionality between 1.5 to 8.
.. . . . . . . . . . . . . . . . . ..
CA 022~7283 1998-ll-30 Preferably between 1.8 to 4.
Specific examples of the polyurethanes are the reaction product~ of a diisocyanate and a polyol.
The diisocyanates suitable for this invention are organic diisocyanates represented by the formula:
R(NC0) 2 wherein the R represents an organic group having a molecular weight of 24 to 2100, preferably 56 to 1000. Preferred diisocyanates according to this invention are tho~e represented by the above formula wherein R represents a divalent aliphatic hydrocarbon group having from 4 to 25 cArho~R, a divalent cycloaliphatic hydrocarbon group having from 4 to 20 carbons, or a divalent araliphatic hydrocarbon group having from 6 to 20 carbons.
Examples of the organic diisocyanate~ which are particularly suitable for the proces~ include ethylene diisocyanate, 1,4-tetramethylene dii~ocyanate, 1,6-hexamethylene diisocyanate, 2,2,4-trimethyl-1,6-hexamethylene diisocyanate, 1,10-decanemethylene diisocyanate, 1,12-dodecanemethylene diisocyanate, cycloheYAne-1,3-diisocyanate, cycloheYAne-1,4-diisocyanate, 1, isocyanato-2-isocyanatomethyl cycl,opentane, isophorone diisocyanate, bis-(4-isocyanatocyclohexyl)-methane, 1,3- and/or 1,4-bis-(isocyanatomethyl)-cyclohPYAne, bis-(4-isocyanato-3-methyl-cyclohexyl)-methane, ~,a,~',a'-tetramethyl, 1,3-and/or 1,4-xylene diisocyanate,l-i~ocyanato-l-methyl-4(3)-isocyanatomethyl cyclohP~YAnP~ 2,4-and/or 2,6-hexahydrotoluylene diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, m- and p-tetramethylxylene diisocyanates, p-xylene /o CA 022~7283 1998-ll-30 diisocyanate, 1,4-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanates, 5-naphthalene diisocyanate. Suitable polyols include those described above as polyesters and polyethers, as well as hydroxyl terminated polylactones, and hydroxyl terminated polycarbonates.
Suitable hydroxyl terminated polylactones are polymeric products of valeratelactone, or ~-caprolactone having molecular weight between 400 and 6000, preferably between 650 and 3,000.
Suitable hydroxyl terminated polycarbonate~ are reaction products obtained from reaction of the polydydric alcohols previously set forth for preparing the polyhydroxyl polyesters with phosgene, diaryl carbonates such diphenyl carbonate or cyclic cArhonAtes such as ethylene or propylene carbonate.
Al~o suitable are polyester cArho~Ates or polyether carbonates obtained by the reaction of lower molecular weight oligomer of the above-mentioned polyesters, polylactones, or polyethers with phosgene, diaryl cArh~nAtes or cyclic carbonates.
The hydroxyl terminated polycarbonates suitable for this invention have molecular weight between 250 to 8,000, preferably between 650 and 3,000.
Specific examples of hydroxyl group-contA;n;ng polyacrylates are the polymers obt A; n~ by polymerization of one or more kind~ of unsaturated hydroxylacrylic monomers (e.g. 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2-hydroxyacrylate), unsaturated acrylic acid amide CA 022~7283 1998-ll-30 W O 97/45475 PCTrUS97/06251 monomer6 (e.g. acrylamide, N-methylolacrylamide, methacrylamide), unsaturated carboxylic acid monomers (e.g. acrylic acid, methacrylic acid, itaconic acid, crotonic acid), unsaturated acid anhydride monomers (e.g. itaconic anhydride, maleic anhydride), unsaturated glycidyl monomers (e.g.
glycidyl acrylate, glycidyl methacrylate), acrylic ester monomers (e.g. ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate), methacrylic ester monomers (e.g. methyl methacrylate, n-lauryl methacrylate, isobutyl methacrylate), maleic ester monomers (e.g. dibutyl maleate, diethyl maleate), fumaric ester monomer6 (e.g. dibutyl fumarate, diethyl fumarate), styrene and its derivatives (e.g.
~-methylstyrene, ~-chloro6tyrene, ~-bromostyrene, p-bromostyrene), nitriles (e.g. acrylonitrile, methylacrylonitrile, ethylacrylonitrile~ and the like.
Specific examples of copoly(urethane-acrylate) are copolymers prepared as described for compo~Pnt (c), except between 2 to 50 percent by weight of component (d) was used a~ the polyol.
The two component coating compositions according to this invention are prepared by m;~;ng of the polyisocyanate, compo~ent (I), into the isocyanate reactive aqueous solution and/or dispersion of hydroxyl terminated polymer, co...~o~ent (II). ~;~r;ng of the two col~ro~nts is suitably carried out by simple stirring or sh~k; ng at room temperature without high energy. The quantity of the polyisocyanate component is selected to provide an NCO/OH equivalent ratio, based on the isocyanate groups of component (I), and the hydroxyl groups of /'~
CA 022~7283 1998-11-30 W 097/45475 PCT~US97/062Sl component (II), of about 1 to 5, preferably about 1.2 to 2Ø The mixtures prepared according to this invention have good pot-life and spray viscosity of more than two hours.
Before polyisocyanate component (I) i8 mixed into isocyanate reactive component (II), the auxiliaries and additives typically used in coating technology may be incorporated into the isocyanate reactive component (II). The auxiliaries and additives include foam inhibitors, leveling aids, pigments, dispersion aids for solid pigments, surface active agents, etc.
The two-component coating compositions according to this invention thus obtained are lS suitable for virtually any applications solvent-cont~in;ng, solventless, or other aqueous paint and coating systems on substrate~ are currently used.
Examples of the applications include the painting and coating of metal surfaces, the painting and coating of plastic surfaces, the painting, coating, or sealing of wood and wood based material~ such as particle board, fiber board and paper, the painting, coating, or sealing of mineral material surfaces such as lime- and/or çement-bound building material and concrete, and the painting and coating of bitumen-cont~;ning pavements. They are also suitable for the ho~ng of various materials wherein the materials of two surfaces may be the same of different.
30- The aqueous coating compositions according to the present invention may be applied to substrates using any of the various techniques known in the art, such as spraying, roll-on, brush-on and 80 on.
....
CA 022~7283 1998-ll-30 W 097/45475 PCT~US97/06251 They can also contain pigments, levelling agents, catalysts, and other auxiliaries known in the art.
The invention i5 further illustrated in, but is not intended to be limited by, the following examples in which all parts and percentages are by weight unless otherwi~e specified.
EXAMPLE 1 - Preparation of a Coating Containing HDI
Dimer Plus HDI Trimer With Solvent.
Step 1 PreParation of Low Vi~cosity HDI Dimer/HDI Trimer Isocyanate Crosslinker The HDI dimer/HDI trimer isocyanate crosslinker was prepared by blen~ing: (a) 100 parts of low viscosity he~methylene diisocyanate (HDI) dimer;
(b) 100 parts of HDI trimer; and (c) 35.29 parts of dipropylene glycol dimethyl ether (commercially available as PROGLYDE DMM, a product of Dow Chemical Company). These materials were stirred for 30 minutes at room temperature.
Step 2 Preparation of the Pol w rethane Ionomer and the Aqueous DisPersion of PolYurethane Resin To an appropriate sized reaction vessel, namely a 3-neck round bottom fla~k, equipped with a stirrer, a temperature control, a co~nRer, and a nitrogen purge, the following five ingredients were charged: (1) polyester polyol in an amount of 110.92 parts (OH eguivalent weight=270.75)~; (2) isophorone /~
CA 022~7283 1998-11-30 W O 97/45475 PCT~US97106251 diisocyanate (IPDI) monomer in an amount of 45.48 part~; (3) dimethylol propionic acid (DMPA) in an amount of 13.60 parts; (4) N-methyl pyrroli~;no~e (NMP) in an amount of 30.OO parts; and, (5) T-12 (dibutlytin dilaurate) catalyst in an amount of 0.10 parts .
This reaction mixture was heated to 80~C and maintained until the NC0 peak was no longer apparent by IR. 185 parts of said ionomer was weighed into an 800mL dispo~able beaker and set aside for preparation of dispersion as follows.
To neutralize the carboxyl concentration in the ionomer, 8.78 parts of dimethylethanolamine (DMEA) was added to a 250mL disposable beaker along with tap water, in an amount of 199.76 parts. This mixture was manually ~tirred into solution with a ~poonula. The io~o~r wa~ placed under moderate agitation using a Premier Mill dispersator equipped with a ~hi-vis" mix head. To this ionomer, the above water/amine solution was charged and dispersed to provide the desired aqueous dispersion of ionomer.
Step 3 PreParation and Te~tinq of Two-ComPonent (2K) PolYurethane-HDI Dimer/HDI Trimer coatinq Crosslinking of the two-component composition was effected by first A~;ng to an eight ounce glass bottle the following ingredients: isocyanate crosslinker (from Step 1 of the present Example) in an amount of 18.17 parts; dispersion of ionomer (from Step 2 of the present Example) in an amount of 66.23 part~; OSi Specialties, Inc.'s SILWET L-7604 .. . . .. . . ..... . . . .
CA 022~7283 1998-11-30 (10% aqueous) in an amount of 0.80 parts; OSi Specialties, Inc.~s SILWET L-7605 (10% aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as Dow Chemical Company's PROGLYDE DMM) in an amount of 12.53 parts; and, water in an amount of 12.40 parts. Standard tests were conducted on the resulting coating, and the results are give in Table 1 below.
The coated test panels were allowed to cure at ambient temperature and humidity conditions for two weeks before testing for appearance, mechanical properties, and chemical resistance. Pencil hardness was determined according to ASTM D3363-92a.
The conical mandrel bend tests were performed using a one-eight inch tester from BYK-Gardner, Inc.
according to ASTM DS22-92. Direct and reverse impact ~alues were determined according to ASTM
D2794-92 using a variable height impact tester from BYR-Gardner, Inc. G1OBB was determined using a micro-TRZ-gloss, multi-angle glossmeter from BYK-Gardner. Cross-hatch adhesion was determined using a cross-hatch cutter from BYK-Gardner according to ASTM D3359-92a. Chemical Resistance was determined according to ASTM D1308-87.
/~
T ~ L~ 1 Physical Pro~ert~ Result Chem. Property Result Thickness (mils) 2.85 CHEMICAL RESISTANCE
Mandrel Bend (1/4n) PASS (10% in water [1/2 hour 20~ Micro-Gloss 84.95 test]) 60~ Micro-Gloss 92.30 Acetic Acid PASS
Impact (direct) ~160 Sodium Hydroxide PASS
Impact (reverse) +160 Hydrochloric Acid PASS
Cross-Hatch PASS SO~VENT RESISTANCE
Max. Pencil Hard. ~9H* (l/2 hour test under 2 n MEK Rub (100 cycles) PASS watch glas~) Xylene PASS
Methyl Ethyl Ketone PASS
* Coating provided "~r-resistance" in 2B-9H Pencil Hardne~s te~t~.
EXAMPLE 2 - Preparation of a Coating Composition Co~tA~ning HDI Dimer P1UB HDI Trimer With No Solvent.
Step 1 PreParation of 100% Solids HDI Dimer/HDI Trimer I~ocYanate Crosslinker To an appropriate reaction vessel, namely a 3-_ neck round bottom fla~k equipped with stirring and a nitrogen purge, the following two ingredients were charged: (1) low viscosity hexamethylene diisocyanate (HDI) dimer in an amount of 35.00 parts; (2) HDI trimer in an amount of 35.00 parts.
These materials were stirred for 30 minutes at room temperature.
/~
CA 02257283 1998-ll-30 W O 97/45475 PCTrUS97/06251 Step 2 Preparation of the Coatinq Com~osition Crossl; nk; n~ followed the procedure as set out in Example 1 above, using ingredient weights that follow: isocyanate crosslinker (see Example 1, Step 1) in an amount of 18.40 parts; dispersion (see Example 1, Step 2) in an amount of 66.23 parts;
SILWET L-7604 (10% aqueous) in an amount of 0.80 parts; SILWET L-7605 (10% aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as PROGLYDE DMM) in an amount of 12.53 parts; and, water in an amount of 12.40 parts, thus forming the desired coating composition having physical and chemical properties as shown in Table 2.
Physical Pro~ertY Result Chem. ProPerty Result Thickness (mils) 2.65 CHEMICAL RESISTANCE
Mandrel Bend (1/4n) PASS (10~ in water [1/2 hour 20~ Micro-Gloss 85.0 te8tl) 60~ Micro-Gloss 81.5 Acetic Acid PASS
Impact (direct) +~60 Sodium Hydroxide PASS
Impact (reverse) +160 Hydrochloric Acid PASS
Cro~s-Hatch PASS SOLVENT RESISTANCE
Max. Pencil Hard. ~9H* (1/2 hour test under 2"
MEK Rub (100 cycles) PASS watch glass) Xylene PASS
Methyl Ethyl Ketone PASS
* Coating provided "mar-resistance" in 2B-9H Pencil Hardness te~t~.
/~
CA 022~7283 l998-ll-30 W O 97/45475 PCTrUS97/06251 EXAMPLE 3 - Preparation of a Coating Composition Cont~;n;ng Allophanate Plus HDI Trimer With No Solvent.
Step 1 Pre~aration of HDI Trimer/AlloPhanate IsocYanate Cro~slinker The following trimer/allophanate variation was prepared using the procedure of Example 1, Step 1, but without solvent:
HDI Trimer 35.00 parts A~OPHANATE 35.00 parts Step 2 PreParation of the Coatinq Com~osition Cros61;nking followed the procedure as set out in Example 1 above, using ingredient weights that follow: isocyanate crosslinker (see Example 1, Step 1) in an amount of 18.86 parts; disper6ion (see Example 1, Step 2) in an amount of 66.23 parts;
SILWET L-7604 (10% aq~eous) in an amount of 0.80 parts; SI~WET ~-7605 (10% aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as PROGLYDE DMM) in an amount of 12.~3 parts; and, water in an amount of 12.40 parts, thus forming the desired coating composition.
.. , . . ~ ~
CA 022~7283 1998-11-30 W 097/45475 PCTrUS97/06251 EXAMPLE 4 - Preparation of a Coating Cont~' ni ng Allophanate P1UB IPDI Trimer.
Step 1 Pre~aration of IPDI Trimer/Allo~hanate IsocYanate Crosslinker The following trimer/allophanate variation was prepared using the procedure of Example 1, Step 1:
IPDI Trimer 35.00 parts ALLOPHANATE 35.00 parts DMM 17.50 parts Step 2 PreParation of the Coatinq Com~osition Crossl; nki ng followed the procedure as set out in Example 1 above, using ingredient weights that follow: isocyanate crosslinker (see Example 1, Step 1) in an amount of 22.88 parts; dispersion (see Example 1, Step 2) in an amount of 66.23 parts;
SILWET L-7604 (10% aqueousJ in an amount of 0.80 parts; SILWET L-7605 l10~ aqueous) in an amount of 0.80 parts; dipropylene glycol dimethyl ether (as PROGLYDE DMM) in an amount of 12.53 parts; and, water in an amount of 12.40 parts, thus forming the desired coating composition.
While the invention has been described above -with reference to specific embodiments thereof, it iB apparent than many changes, modifications and variations can be made without departing from the inventive concept disclosed herein. Accordingly, it ~1 CA 02257283 1998-ll-30 i8 intended to embrace all such changes, modifications and variations that fall within the spirit and broad scope of the appended claim~.
. , .. ~ .... . .
Claims (17)
1. A two-component aqueous polyurethane coating composition that is curable into a coating exhibiting enhanced hardness, gloss, and solvent resistance, said coating composition characterized by:
(I) a polyisocyanate which is dispersible in an aqueous polymer resin dispersion, has an average functionality of at least 2.0 and contains:
(A) 25% to 95% by weight of a polyisocyanate adduct selected from the group consisting of cyclodimers or allophanates of 3,3,5-trimethylhexmathylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinations thereof, and (B) 5% to 75% by weight of another polyisocyanate adduct selected from the group consisting of cyclotrimers or biurets of 3,3,5-trimethylhexamethylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinations thereof, and, (C) 0% to 30% by weight of an organic solvent that is inert to isocyanate; and, (II) an isocyanate reactive hydroxyl-terminated, water dispersable polymer resin having a hydroxyl number of between 10 and 450 (preferably between 28 and 350), with the proviso that if component (B) consists essentially of cyclotrimerized isophorone diisocyanate, then component (C) is present in an amount of at least 10% by weight, based upon the weight of said coating composition.
(I) a polyisocyanate which is dispersible in an aqueous polymer resin dispersion, has an average functionality of at least 2.0 and contains:
(A) 25% to 95% by weight of a polyisocyanate adduct selected from the group consisting of cyclodimers or allophanates of 3,3,5-trimethylhexmathylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinations thereof, and (B) 5% to 75% by weight of another polyisocyanate adduct selected from the group consisting of cyclotrimers or biurets of 3,3,5-trimethylhexamethylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinations thereof, and, (C) 0% to 30% by weight of an organic solvent that is inert to isocyanate; and, (II) an isocyanate reactive hydroxyl-terminated, water dispersable polymer resin having a hydroxyl number of between 10 and 450 (preferably between 28 and 350), with the proviso that if component (B) consists essentially of cyclotrimerized isophorone diisocyanate, then component (C) is present in an amount of at least 10% by weight, based upon the weight of said coating composition.
2. A two-component aqueous polyurethane coating composition that is curable into a coating exhibiting enhanced hardness, gloss, and solvent resistance, said coating composition characterized by:
(I) a polyisocyanate which is dispersible in an aqueous polymer resin dispersion, has an average functionality of at least 2.0 and contains:
(A) 25% to 95% by weight of a polyisocyanate adduct selected from the group consisting of cyclodimerized 1,4-tetramethylene diisocyanate, cyclodimerized 1,6-hexamethylene diisocyanate, 1,4-tetramethylene diisocyanate allophanate, 1,6-hexamethylene diisocyanate allophanate, and combinations thereof, and (B) 5% to 75% by weight of another polyisocyanate adduct selected from the group consisting of cyclotrimerized hexamethylene diisocyanate, hexamethlyene diisocyanate biuret, cyclotrimerized isophorone diisocyanate, isophorone diisocyanate biuret, and combinations thereof, and, (C) 0% to 30% by weight of an organic solvent that is inert to isocyanate; and, (II) an isocyanate reactive hydroxyl-terminated, water dispersable polymer resin having a hydroxyl number of between 10 and 450, with the proviso that if component (B) consists essentially of cyclotrimerized isophorone diisocyanate, then component (C) is present in an amount of at least 10% by weight, based upon the weight of said coating composition.
(I) a polyisocyanate which is dispersible in an aqueous polymer resin dispersion, has an average functionality of at least 2.0 and contains:
(A) 25% to 95% by weight of a polyisocyanate adduct selected from the group consisting of cyclodimerized 1,4-tetramethylene diisocyanate, cyclodimerized 1,6-hexamethylene diisocyanate, 1,4-tetramethylene diisocyanate allophanate, 1,6-hexamethylene diisocyanate allophanate, and combinations thereof, and (B) 5% to 75% by weight of another polyisocyanate adduct selected from the group consisting of cyclotrimerized hexamethylene diisocyanate, hexamethlyene diisocyanate biuret, cyclotrimerized isophorone diisocyanate, isophorone diisocyanate biuret, and combinations thereof, and, (C) 0% to 30% by weight of an organic solvent that is inert to isocyanate; and, (II) an isocyanate reactive hydroxyl-terminated, water dispersable polymer resin having a hydroxyl number of between 10 and 450, with the proviso that if component (B) consists essentially of cyclotrimerized isophorone diisocyanate, then component (C) is present in an amount of at least 10% by weight, based upon the weight of said coating composition.
3. The composition of claim 1 characterized in that said polyisocyanate adduct of component (A) is an uretidione or an allophanate, or a combination thereof, prepared from hexamethylene diisocyanate.
4. The composition of claim 3 characterized in that the aliphatic diisocyanate are 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, and combinations thereof.
5. The composition of claim 3 characterized in that the adduct has an average isocyanate content of between 16 to 25, preferably between 18 to 23.
6. The composition of claim 1 characterized in that the polyisocyanate additionally contains isocyanurates, allophanates, uretidiones or biurets prepared from organic diisocyanates represented by the formula:
R(NC0)2 wherein R represents a divalent aliphatic hydrocarbon group having from 4 to 25 carbons, a divalent cycloaliphatic hydrocarbon group having from 4 to 20 carbons, or a divalent araliphatic hydrocarbon group having from 6 to 20 carbons.
R(NC0)2 wherein R represents a divalent aliphatic hydrocarbon group having from 4 to 25 carbons, a divalent cycloaliphatic hydrocarbon group having from 4 to 20 carbons, or a divalent araliphatic hydrocarbon group having from 6 to 20 carbons.
7. The composition of claim 5 characterized in that said diisocyanate is selected from the group consisting of 2,2,4-trimethyl-1,6-hexamethylene diisocyanate, 4,4'-diisocyanatodicyclohexylmethane, 3,3,5-trimethylhexamethylene diisocyanate, 2-methylhexamethylene diisocyanate, isophorone diisocyanate, and combinations thereof.
8. A coated article prepared by contacting a substrate with the coating composition of claim 1.
9. The composition of claim 1 characterized in that said organic solvent is selected from the group consisting of acetone, methylamyl ketone, methylethyl ketone, methyisobutyl ketone, n-methylpyrrolidone, dimethylformamide, dimethylacetamide, n-butylacetate, dipropylene glycol dimethyl ether, propylene glycol methylethylacetate, propylene glycol methylether, xylene, and combination thereof.
10. The composition of claim 1 characterized in that the hydroxyl-terminated, water dispersable polymer resin is selected from the group of resins represented by the formula:
R1(OH)n wherein R1 represents a moiety selected from the group consisting of polyester, a polyether, a polyurethane, a polyacrylate, a copoly(urethane-acrylate), and combinations thereof.
R1(OH)n wherein R1 represents a moiety selected from the group consisting of polyester, a polyether, a polyurethane, a polyacrylate, a copoly(urethane-acrylate), and combinations thereof.
11. The composition of claim 9 characterized in that the molecular weight of the hydroxyl-terminated, water dispersable polymer resin is between 150 and 8,000.
12. The composition of claim 10 characterized in that the molecular weight of the hydroxyl-terminated, water dispersable polymer resin is between 650 and 5,000.
13. The composition of claim 10 characterized in that the functionality of the hydroxyl-terminated, water dispersable polymer resin is between 1.8 and 8.
14. The composition of claim 10 characterized in that the functionality of the hydroxyl-terminated, water dispersable polymer resin is between 2 and 6.
15. The composition of claim 10 characterized in that said R1 is polyurethane.
16. The composition of claim 10 characterized in that said R1 is copoly(urethane-acrylate).
17. A process for preparing a coating composition characterized by contacting component (I) and component (II) of said two-component aqueous polyurethane coating composition of claim 1 to provide a mixture, and admixing said mixture.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65693996A | 1996-05-30 | 1996-05-30 | |
| US656,939 | 1996-05-30 | ||
| PCT/US1997/006251 WO1997045475A1 (en) | 1996-05-30 | 1997-04-07 | Two-component waterborne polyurethane coating |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2257283A1 true CA2257283A1 (en) | 1997-12-04 |
Family
ID=24635204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002257283A Abandoned CA2257283A1 (en) | 1996-05-30 | 1997-04-07 | Two-component waterborne polyurethane coating |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0907673A4 (en) |
| JP (1) | JP2000514469A (en) |
| KR (1) | KR100509342B1 (en) |
| CN (1) | CN1230971A (en) |
| AU (1) | AU2669997A (en) |
| BR (1) | BR9709486A (en) |
| CA (1) | CA2257283A1 (en) |
| WO (1) | WO1997045475A1 (en) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6005045A (en) * | 1998-02-24 | 1999-12-21 | Ppg Industries Ohio, Inc. | Waterborne, ambient temperature curable film-forming compositions |
| DE10012826A1 (en) | 2000-03-16 | 2001-09-20 | Bayer Ag | Adhesive preparations |
| DE10020160A1 (en) * | 2000-04-25 | 2001-10-31 | Bayer Ag | Adhesive preparations |
| EP1445271B1 (en) * | 2001-09-20 | 2008-11-12 | Asahi Kasei Chemicals Corporation | Polyisocyanate composition having allophanate group and high-solid coating material |
| DE10152723A1 (en) | 2001-10-25 | 2003-05-15 | Degussa Construction Chem Gmbh | Aqueous, highly cross-linked two-component polyurethane coating system with reduced hydrophilicity and improved chemical resistance, process for its production and its use |
| US9207373B2 (en) | 2007-04-10 | 2015-12-08 | Stoncor Group, Inc. | Methods for fabrication and highway marking usage of agglomerated retroreflective beads |
| CH705596A1 (en) | 2011-10-06 | 2013-04-15 | Eternit Schweiz Ag | 2-component coating to the fiber cement. |
| JP2015048459A (en) * | 2013-09-04 | 2015-03-16 | Dic株式会社 | Radically polymerizable resin composition and civil engineering building material |
| EP3297773B1 (en) | 2015-05-22 | 2021-06-09 | BASF Coatings GmbH | Aqueous base paint for making a coating |
| WO2016188656A1 (en) * | 2015-05-22 | 2016-12-01 | Basf Coatings Gmbh | Method for producing a multilayer coating |
| US20180258315A1 (en) * | 2015-09-23 | 2018-09-13 | Basf Se | Two-component coating compounds |
| WO2018105653A1 (en) * | 2016-12-07 | 2018-06-14 | 旭化成株式会社 | Polyisocyanate composition and coating composition |
| CN108219658A (en) * | 2017-12-28 | 2018-06-29 | 姜菊芳 | A kind of corrosion-resistant polyurethane coating and preparation method thereof |
| KR102218035B1 (en) * | 2019-05-24 | 2021-02-19 | 한국생산기술연구원 | Polyurethane based self-healing clear coat composition and manufacturing method thereof |
| CN112210282A (en) * | 2020-09-24 | 2021-01-12 | 上海展辰涂料有限公司 | Water-based two-component white-top high-gloss paint with high construction universality and preparation method thereof |
| JP7067602B1 (en) | 2020-12-15 | 2022-05-16 | 亜細亜工業株式会社 | Urethane coating waterproof top coat composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8401785A (en) * | 1984-06-04 | 1986-01-02 | Polyvinyl Chemie Holland | PROCESS FOR PREPARING AN AQUEOUS DISPERSION OF URETHAN ACRYLATE ENTCOPOLYMERS AND STABLE AQUEOUS DISPERSION THUS OBTAINED. |
| DE4001783A1 (en) * | 1990-01-23 | 1991-07-25 | Bayer Ag | POLYISOCYANATE MIXTURES, A PROCESS FOR THEIR PRODUCTION AND THEIR USE AS A BINDER FOR COATING AGENTS OR AS A REACTION PARTNER FOR ISOCYANATE GROUPS OR CARBOXYL GROUPS REACTIVE COMPOUNDS |
| DE4118231A1 (en) * | 1991-06-04 | 1992-12-10 | Bayer Ag | AQUEOUS COATING AGENTS AND ITS USE |
| DE4136618A1 (en) * | 1991-11-07 | 1993-05-13 | Bayer Ag | Water-dispersible polyisocyanate mixtures |
| DE4137429A1 (en) * | 1991-11-14 | 1993-05-19 | Bayer Ag | WAFEREN BINDER COMBINATION, A METHOD OF MANUFACTURING THEM AND THEIR USE |
| US6160076A (en) * | 1994-06-24 | 2000-12-12 | Arco Chemical Technology, L. P. | Cross-linked aqueous polyurethane dispersions containing dimer/trimer |
-
1997
- 1997-04-07 CN CN97196951A patent/CN1230971A/en active Pending
- 1997-04-07 KR KR10-1998-0711018A patent/KR100509342B1/en not_active IP Right Cessation
- 1997-04-07 JP JP09542359A patent/JP2000514469A/en not_active Ceased
- 1997-04-07 BR BR9709486A patent/BR9709486A/en not_active Application Discontinuation
- 1997-04-07 EP EP97918640A patent/EP0907673A4/en not_active Withdrawn
- 1997-04-07 CA CA002257283A patent/CA2257283A1/en not_active Abandoned
- 1997-04-07 AU AU26699/97A patent/AU2669997A/en not_active Abandoned
- 1997-04-07 WO PCT/US1997/006251 patent/WO1997045475A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| BR9709486A (en) | 1999-08-10 |
| JP2000514469A (en) | 2000-10-31 |
| KR100509342B1 (en) | 2005-12-19 |
| CN1230971A (en) | 1999-10-06 |
| KR20010009016A (en) | 2001-02-05 |
| AU2669997A (en) | 1998-01-05 |
| EP0907673A1 (en) | 1999-04-14 |
| WO1997045475A1 (en) | 1997-12-04 |
| EP0907673A4 (en) | 1999-11-10 |
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