BACKGROUND OF THE INVENTION Heretofore, it has been desirable to apply highly crosslinked coatings to the decorative laminates since such coatings exhibit good durability properties such as abrasion resistance and mar resistance as well as increase chemical resistance to solvents and cleaners. A common application for such decorative laminates involves thermoforming the laminate which desirably has a PVC substrate to an end product such as a molded part. However, such highly crosslinked coatings are subject to cracking after they are stretched during the thermoforming process.

US Patent No. 5,780,117 relates to radiation-curable latex composi- tions having a secondary curing mechanism. In these compositions, an anionically stabilized, water-borne dispersion of one or more radiation- curable resins is combined with a low molecular weight compound hav- ing at least two reactive functional groups, wherein one reactive func- tional group comprises an epoxy and the other reactive functional group comprises either an epoxy or a functionality capable of self- condensation after film formation. Also disclosed is a method for providing a cross-linked protective coating on a substrate, wherein a coating of the composition of the present invention is applied to the substrate, the coated substrate is exposed to actinic radiation to effect

strate, the coated substrate is exposed to actinic radiation to effect cur- ing, and then the unexposed or underexposed portions of the coated substrate are allowed to cure at room temperature or greater.

European Disclosure 00331409 relates to a process for producing a polyester film having a thin cured polyurethane coating, which com- prises (1) applying an aqueous composition comprising a thermosetting polyurethane prepolymer as a film-forming component to at least one surface of an unoriented aromatic polyester film to form a thin wet coating on it, said polyurethane prepolymer being characterized by (i) having a polyol component at least 10% by weight of which is com- posed of a polyol containing a carbon-carbon double bond selected from unsaturated polyester polyols and polybutadiene polyols, the carbon- carbon double bond being cleavable under ultraviolet light, (ii) having a pendant anionic hydrophilic group in the polymer chain, and (iii) having isocyanate groups blocked with an oxime at the ends of the polymer chain, and (2) thereafter stretching and heat-setting the coated film, during which time the wet coating of the aqueous composition is dried and the polyurethane prepolymer is cured to form a thin cured polyure- thane coating having a carbon-carbon double bond on the biaxially ori- ented polyester film.

US Patent No. 4,1 07, 013 relates to an improved ultraviolet curable aqueous latex paint suitable for use as coil coatings comprising a high molecular weight primary latex binder in combination with minor amounts of an emulsified low molecular weight cross-linking agent adapted to cross-link the high molecular weight latex particles upon ex- posure to ultraviolet energy.

SUMMARY OF THE INVENTION The composition of the present invention generally com- prises a co-mingled polyurethane-polyvinyl ester composition, which has

improved thermoforming properties, and has good flexibility, good scratch and abrasion resistance, and can have low gloss when contain- ing flattening agents. The composition is derived from a waterborne polyurethane to which is added a free radical, radiation polymerizable monomers or oligomers such as various acrylates. A photoinitiator is desirable utilized in order to permit the free radical polymerizable monomers to be polymerized by ultraviolet light. Optionally, a urethane thermal-crosslinking agent can be added to the waterborne polyure- thane. Generally, the aqueous polyurethane is coated on a substrate such as plastic or paper and dried in order to eliminate water. The free radical monomers or oligomers are then cured by radiation such as UV light to form a laminate. The laminate can then thermoformed onto an end product generally under heat.

DETAILED DESCRIPTION OF THE INVENTION The waterborne polyurethanes of the present invention are commercially available. They are generally chain extended ure- thanes made by the reaction of one or more polyisocyanates with one or more polyol terminated intermediates and also one or more hydroxyl terminated aqueous dispersants which serve to disperse the polyure- thane in water.

The polyol intermediate is generally a polyether polyol, a polythiolether polyol, a polyacetal polyol, a polyolefin polyol, an or- ganic polyol, or a polyester polyol, or preferably a polycarbonate polyol, or combinations thereof, desirably having primary hydroxy end groups and having a number average molecular weight of from about 400 to about 15,000 and desirably from about 2,000 to about 9,000.

The polyether polyols generally contain from 2 to 10 car- bon atoms. Such polyols include polyoxypropylene diols and triols, poly (oxyethylene-oxypropylene) diols and triols, and the like.

Poloythioether polyols which can be used include prod- ucts obtained by condensing thiodiglycol either alone or with other glycols, dicarboxylic acids, formaldehyde, aminoalcohols or aminocar- boxylic acids.

Polyacetal polyols which can be used include those pre- pared by reacting glycols such as diethylene glycol, triethylene glycol and hexanediol with formaldehyde. Suitable polyacetals may also be prepared by polymerizing cyclic acetals.

Suitable polyolefin polyols include hydroxy-terminated bu- tadiene homo-and copolymers.

Organic polyols having molecular weights below 400 can also be used in the preparation of the prepolymers particularly include diols and triols and mixtures thereof but higher functionality polyols may be used. Examples of such lower molecular weight polyols in- clude ethylene glycol, diethylene glycol, tetraethylene glycol bis (hydroxythyl) terephthalate, cyclohexane dimethanol, furan di- methanol, glycerol and the reaction products, up to molecular weight 399, of such polyols with propylene oxide and/or ethylene oxide.

The preferred polycarbonate polyols which can be used include products obtained by reacting diols having from 2 to 10 car- bon atoms such as 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, diethyene glycol or tetraethylene glycol with diaryl carbonates having from 1 3 to 20 carbon atoms, for example diphenyl carbonate, or with phosgene.

The polyester polyols are typically formed from the con- densation of one or more polyhydric alcohols having from 2 to 18 car- bon atoms and preferably from 2 to 6 carbon atoms with one or more polycarboxylic acids or their anhydrides having from 2 to 14 carbon atoms. Examples of suitable polyhydric alcohols include the following: ethylene glycol, propylene glycol such as 1,2-propylene glycol and 1,3-propylene glycol, glycerol ; pentaerythritol ; trimethylolpropane ;

1,4,6-octanetriol; butandiol ; pentanediol ; hexanediol ; dodecanediol ; octandiol ; chloropentanediol, glycerol monoallyl ether; glycerol mono- ethyl ether, diethylene glycol ; 2-ethylhexanediol-1, 4; cyclohexanediol- 1,4; 1,2,6-hexanetriol; neopental glycol ; 1,3,5-hexanetriol; 1,3-bis- (2- hydroxyethoxy) propane and the like. Cyclic ethers with desirably 2 to 18 carbon atoms may be used instead, but they are more expensive to use. Examples of polycarboxylic acids include the following : phthalic acid; isophthalic acid; terephthalic acid; tetrachlorophthalic acid; maleic acid; dodecylmaleic acid; octadecenylmaleic acid; fumaric acid; aconitic acid; trimellitic acid; tricarballylic acid; 3,3'-thiodipropionic acid; succinic acid; adipic acid; malonic acid, glutaric acid, pimelic acid, sebacic acid, cyclohexane-1, 2-dicarboxylic acid; 1,4- cyclohexadiene-1, 2-dicarboxylic acid; 3-methyl-3, 5-cyclohexadiene- 1,2-dicarboxylic acid and the corresponding acid anhydrides, acid chlorides and acid esters such as phthalic anhydride, phthaloyl chlo- ride and the dimethyl ester of phthalic acid. Polyesters from lactones (for example caprolactone) can also be used.

Preferred intermediates include polyester intermediates made from acids such as adipic acid or phthalic acid or isomers thereof with glycols such as ethylene glycol, propylene glycol, buty- lene glycol, diethylene glycol, hexamethylene glycoi, trimethy- lolethane, or trimethylolpropane. Specific preferred polyester interme- diates include poly (ethylene adipate) glycol, poly (diethylene adi- pate) glycol, poly (ethylene/propylene adipate) glycol, poly (propylene adipate) glycol, poly (butylenes adipate) glycol, poly (neopentyl adi- pate) glycol, poly (hexamethylene adipate) glycol, poly (hexamethylene/neopentyl adipate) glycol, and the like.

The hydroxyl terminated or polyol dispersant can gener- ally be any organic compound which contains one or more carboxyl groups and two or more hydroxyl groups such as a carboxyl group containing diol or triol. Generally, such compounds can contain a total of from about 4 to about 24 carbon atoms with from about 4 to about 8 carbon atoms being preferred. And example of such a suitable dis- persant has the formula

wherein R is hydrogen or alkyl containing from 1 to about 16 carbon atoms. A preferred carboxy containing diol is 2,2-dimethylol propionic acid. If desired, the carboxy containing diol or triol can be incorpo- rated into a polyester by reaction with a dicarboxylic acid before being incorporated into the prepolymer. Useful compounds include the fu- marate polyether glycols described in U. S. Patent No. 4,460,738.

Other useful carboxy-containing compounds include aminocarboxylic acids, for example lysine, cystine and 3,5-diaminobenzoic acid.

The one or more polyisocyanates which are utilized gen- erally have the formula R (NCO) n where n usually is an integer of 2,3 or 4 with approximately 2 being preferred. However, it is to be under- stood that since combinations of various polyisocyanates can be util- ized, the equivalent amount of isocyanate can vary and often n is not an integer. R is an aliphatic having from about 2 to about 20 carbon atoms with from about 6 to about 15 carbon atoms being preferred, an aromatic including an alkyl substituted aromatic having from about 6 to about 20 carbon atoms with from about 6 to about 12 carbon atoms being preferred, or combinations thereof. Aliphatic diisocy- anates are preferred inasmuch aromatic diisocyantes tend to yellow.

Examples of suitable polyisocyanates include hexamethylene diisocy- anate, 2,2,4- and/or 2,4,4-trimethyl hexamethylene diisocyanate, p- and m-tetramethyl xylene diisocyanate, methylene bis (4-cyclohexyl isocycante) (hydrogenated MDI), 4,4-methylene diphenyl isocyanate (MDI) mixtures of MDI with polymeric MDI having an average isocy- anate functionality of from about 2 to about 3.2, p-and m-phenylene

diisocyanate, 2,4- and/or 2,6-toluene diisocyanate (TDI), and iso- phorone diisocyanate (IPDI). Also useful are diisocyanates prepared by capping low molecular weight compounds, that is less than 300, such as £-caprolactam, butanone oxime, phenol, etc., with diisocy- anates. Any combination of polyisocyanates can be employed. Pre- ferred polyisocyanates include aliphatic diisocyanates such as iso- phorone diisocyanate.

The equivalent weight ratio of the one or more diisocy- anates to the one or more polyol intermediates as well as the one or more organic dispersants can be from about 0.8 to about 1.2, and de- sirably from about 0.9 to about 1.1. The mole ratio of the at least one organic dispersant is from about 0.35 to about 3.0, desirably from about 0.5 to about 2.0, and preferably from about 0.80 to about 1.2 moles per mole of the one or more polyol intermediates.

The reaction conditions of forming the polyurethane are generally known to the art and to the literature and include a reaction temperature from about 110°C to about 320°C, desirably from about 125 to about 210°C, and preferably from about 140°C to about 175°C. Catalysts are desirably utilized and include conventional compounds such as dibutyl tin dilaurate, stannous octoate, diazabicy- clo (2.2.2) octave (DABCO), Zn ACAC., tin octoate, and the like The amount of catalyst is small, generally from about 0.005 to about 0.2 parts by weight per 100 parts by weight of the urethane forming monomers. Any suitable solvent can be utilized in the urethane for- mation such as N-methyl-pyrrolidone, toluene, and the like.

Once the one or more polyurethanes has been formed, they are converted into an aqueous solution or dispersion. To obtain good solubility or dispersability in water, a neutralizing agent is added to the polyurethane solution. Neutralizing agents include inorganic bases such as ammonium, amine, and the like. When amine neutraliz-

ing agents are utiiiz ; : d, a number of amine groups therein can generally range from about 1 to about 3 or 4 and the total number of carbon atoms can range from about 2 or 3 to about 12. Inorganic bases in- clude sodium hydroxide and potassium hydroxide, while the amines, in addition to ammonia include trimethylamine, triethylamine and di- methylethanolamine. The neutralizing agent can be used in either substoichiometric or excess quantities. Accordingly, the stoichiomet- ric ratio can generally vary from about 0.9 to about 1.2 and preferably from about 1.0 to about 1.05. Use of the neutralizing agent changes the dispersant, for example the carboxyl group containing diol and triol, into a salt thereby generally rendering the polyurethane dispersi- ble in water.

Only after the polyurethane has been neutralized, can water be added thereto to form a waterborne polyurethane solution.

The amount of water is generally such that the solid content of the solution is generally from about 20 or 30 to about 65, and preferably from about 35 to about 50 percent by weight.

While optional, it is desirable to chain extend the various above noted polyurethanes. The chain extender can be a polyol, an amino-alcohol, ammonia, a primary or secondary aliphatic, alicyclic, aromatic, aryaliphatic or heterocyclic amine, especially a diamine, hy- drazine or a substituted hydrazine.

Examples of suitable chain extenders useful herein in- clude ethylene diamine, diethylene triamine, triethylene tetramine, propylene diamine, butylen diamine, hexamethylene diamine, cyclo- hexylen diamine, piperazine, 2-methyl piperazine, phenylen diamine tolylene diamine, xylylen diamine, tris (2-aminoethyl) amine, 3,3'- dinitrobenzidine, 4,4'-methylenebis (2-chloroaniline), 3,3'dichloro-4,4'- bi-phenyl diamine, 2,6-diaminopyridine, 4,4'-diaminophinylmethane, methane diamine, m-xylene diamine, or isophorone dimine, or combi- nations thereof.

The chain extension can be conducted at elevated, re- duced or ambient temperatures as from about 5°C to about 95°C, or preferably from about 10°C to about 45°C.

The above formed and chain extended compounds are anionic waterborne polyurethanes dispersions which generally have low viscosities, i. e. less than 500 centipoises, and desirably from about 60 to about 400 centipoise, and preferably from about 120 to about 300 centipoise.

The above noted waterborne aliphatic urethane polymers are commercially available such as Neorez 9603 from Avecia; as well as R-960, A-1049, and R-9649 all from Avecia; Bayhydrol 123 from Bayer, Flexthane 620 and 630 from Air Products, and the like.

The free radical, UV polymerizable monomers and/or oli- gomers of the present invention are made by the free radical polymeri- zation of unsaturated monomers or oligomers having a total of from 2 to 150 carbon atoms, desirably from about 3 to about 75, and pref- erably from about 6 to 20 carbon atoms such as an ester of a ethylenically unsaturated carboxylic acid, often referred to as a vinyl ester, such as acrylate and/or methacrylate, and especially alkoxylated (meth) acrylate where said"meth"group mat or may not exist. These monomers and/or oligomers can generally be classified as monofunc- tional, difunctional, trifunctional, and multifunctional such as mono- functional, difunctional ; etc., acrylates. It is to be understood that whenever the term" (meth)" is utilized, that the utilization of the methyl group in a compound is optional.

Examples of suitable monofunctional monomers include various acrylates such as 2-phenoxyethyl acrylate, ethoxylated phenol monoacrylate, lauryl acrylate, hexadecyl acrylate, stearyl acrylate, tripropylene glycol, methylether monoacrylate, neopentylglycol pro- poxylate (2) methylether monoacrylate, propoxylated (2-20) nonylphenol

monoacrylate, and the like. Examples of other suitable alkyl (meth) acrylates have from 1-20 carbon atoms in the alkyl group and include methyl (meth) acrylate, ethyl (meth) acrylate, pro- pyl (meth) acrylate, isopropyl (meth) acrylate, butyl (meth) acrylate, 2- ethyl (meth) acrylate, octyl (meth) acrylate, isobornyl (meth) acrylate, do- decyl (meth) acrylate, isobornyl acrylate, and cyclohexyl (meth) acrylate, and the like. Examples of suitable (meth) acrylates having ether groups include 2-methoxy-ethylmethacrylate, 2-ethoxyethylmethacrylate, and 3-methoxy-propylmethacrylate, and the like. Examples of suitable hy- droxyalkyl (meth) acrylates include 2-hydroxethyl (meth) acrylate, 2- hydroxypropyl (meth) acrylate, 4-hydroxybutylacrylate, 6- hydroxyhexylacrylate, p-hydroxycyclohexyl (meth) acrylate, hydroxy- polyethylene glycol (meth) acrylates, hydroxypolypropylene gly- col (meth) acrylates and alkoxy derivatives thereof, and the like.

Examples of difunctional compounds include various acry- lates such as 1-6-hexanediol diacrylate, bispheonol A ethoxylated dia- crylate, polyethylene glycol diacrylate (200-600), tripropylene glycol diacrylate, neopentylglycol propoxylate (2) diacrylate, ethoxylated (2) neopentyl glycol diacrylate, dipropylene glycol diacrylate, trimethylol- propane ethoxylated (3) methyether diacrylate, and the like.

Examples of trifunctional compounds include various acrylates such as trimethylolpropane triacrylate, trimethylolpropane propoxylate (5-20) triacrylate, propoxylated (4) glycerol triacrylate, eth- oxylated (3) trimethylolpropane triacrylate, propoxylated pentaerythri- tol triacrylate, and the like.

Examples of tetrafunctional compounds include various acrylates such as ditrimethylolpropane tetraacrylate, dipentaerythritol monohydroxy pentaacrylate, and the like.

Suitable substituted (meth) acrylate compounds include (meth) acrylamide, (meth) acrylonitrile, N-methylol (meth) acrylamide, and N-alkyl (meth) acrylamides, and the like. Other suitable compounds

which are simply classified as mono-unsaturated compounds include vinylchloride, vinylacetate, vinylpropionate, as well as vinylpyrrolidone, and the like.

A preferred class of free radical free polymerizable oli- gomers of the various above noted alkoxylated (meth) acrylate mono- mers generally contain 2 to about 4 or more acrylate and/or methacry- late groups or combinations of the same within the same oligomer.

The ester portion of the acrylate is generally an aliphatic and desirably an alkyl having from 1 to about 10 carbon atoms. The acrylates are alkoxylated, meaning that they contain one or more alkoxy groups be- tween the acrylate end groups and often times have a core or nucleus compound therein as known to the art and the literature such as neopentyl glycol or tripropylene glycol pentaerythritol. Generally the number of alkoxyl groups within the compound is from about 3 to about 50 with from about 3 to about 20 being preferred. Suitable alkoxy groups generally include methoxy, or ethoxy, or propoxy. Such alkoxylated acrylates are commercially available as Sartomer SR9035, SR399, SR444, and the like, all from Sartomer.

Other monomers and oligomers include urethane acry- lates, epoxy acrylates, epoxy methacrylates, acrylate epoxy oli- gomers, acrylate aliphatic urethane oligomers, acrylate aromatic urethane oligomers, acrylate polyesters oligomers, acrylate acrylic oligomers, methacrylates, and the like.

The amount of the one or more free radically polymer- able monomers or oligomers such as the above noted vinyl esters as well as the alkoxylated acrylate monomers, is generally from about 5 to about 75, desirably from about 12 to about 60, and preferably from about 18 to about 45 parts by weight for every 100 parts by weight of the polyurethane.

A class of suitable radiation initiators such as photoinitia- tors, or combinations of photoinitiators and photoactivators include

benzophenone and substituted benzophenones, benzoin and its deriva- tives such as benzoin butyl ether and benzoin ethyl ether, benzil ketals such as benzil dimethyl ketal acetophenone derivatives such as a, a- diethoxyacetophenone and a, a-dimethyl-a-hydroxyacetophenone, benzoates such as methyl-o-benzoyl benzoate, thioxaothones, Michler's ketone, and acylphosphine oxides or bis-acylphosphine ox- ides. Examples of other photo initiators include hydroxylcyclohexyl phenyl ketone (HCPK), 2-benzyl-2-N, N-dimethylamino-1- (4-morpholino phenyl)-1-butanone (DBMP), 1-hydroxyl cyclohexyl phenyl ketone, beozophenone, 2-methyl-1- (4-methylthio) phenyl-2-morpholino propan- 1-onc (MMP), and the like.

Ultraviolet light free radical initiators also include the various nitrogen containing compounds such as AIBN (Azobisbeleroni- trile and Azobutyronitrile) Should the vinyl ester be reacted by heat instead of ra- diation, then in lieu of the ultraviolet light free radical initiators, etc., thermal free radical initiators such as various peroxides can be utilized as for example benzoyl peroxide, t-butyl peroxypivalate, 2,4-dichloro- benzoyl peroxide, decanoylperoxide, propionyl peroxide, hydroxyheptyl peroxide, cyclohexanone peroxide, 2,5-dimethylhexyl-2,5-di (proxy- benzoate), t-butyl perbenzoate, dicumyl peroxide, 2,5-dimethyl-2,5- di (t-butylperoxy) hexyne-3,2,5-di-methyl 2,5-di (t-butylperoxy) hexane, 3,5-dimethyl-2,5-di (benzoyl-peroxy) hexane, di-t-butyl peroxide, p- menthane hydro-peroxide, cumene hydroperoxide, 2,5-dimethyl-2,5- di (hydroxperoxy) hexane, t-butyl hydroperoxide, lauroyl peroxide, t- amyl perbenzoate, or mixtures thereof. Preferred organic peroxides are benzoyl peroxide and t-butyl perbenzoate.

The amount of the various photo initiators such as ultra- violet light initiators or thermal initiators is generally from about 0.5 to about 15, desirably from about 2 to about 10, and preferably from

about 4 to about 8 parts by weight per 100 parts by weight of the one or more different polymerizable monomers or oligomers such as the alkoxylated acrylates.

The above noted free radical polymerizable monomers or oligomers as well as the initiators therefore are added to the water- borne polyurethane solution and mixed. Optionally, in addition thereto, various other additives can be added to impart favorable end properties to the resulting co-mingled polyurethane-addition polymer composition. Such additives include various urethane crosslinking agents, various flattening agents, various scratch and/or mar resistant agents, wetting agents, and the like.

The various urethane crosslinking agents are desirably thermally activated and include compounds such as various (poly) aziridines, (poly) carbodimides, epoxies, melamine-formaldehyde, (poly) isocyanates, or (poly) amines, and the like. As used herein, the term aziridine refers to any alkyleneimine and includes any compound based on the following structure: where R, independently, is hydrogen, an alkyl radical having 1 to 3 carbon atoms, phenyl or combinations thereof.

Preferably, the aziridine is based on the following struc- ture:

wherein R, is as described above and R2 is hydrogen or an alkylen radical having 1 to 4 carbon atoms. Such aziridines include ethyle- neimine, ethyl ethyleneimine and propyleneimine. The aziridine com- pound of the present invention also includes polyfunctional aziridines.

Particularly useful polyfunctional aziridines include trimethylolpropane- tris- (B- (N-aziridinyl) propionate) and pentacrythritol-tris (B (N- aziridinyl) propionate) which are available commercially from Virginia Chemicals of Portsmouth, VA as XAMA-2 and XAMA-7, respectively.

A highly preferred aziridine is available as CX100 from Avecia.

Examples of suitable (poly) carbodimides include multi- functional carbodimides such as Ucarlnk XL-29SE from Union Carbide.

Examples of suitable epoxies include bisphenol A types such as Epon 828 and 825 from Shell. Examples of suitable polyisocyanates in- clude Desmodur DA (1,6-hexamethylene diisocyanate based polyiso- cyanates). Examples of suitable melamine formaldehydes include me- thylated melamine formaldehyde such as Cymel 373,303, and 385 from Cytec, and Resimene from Solutia.

Such urethane crosslinking agents are thermally activated such as at temperatures of from about 80°F to about 350°F, and from about 140°F to about 180°F. When activated, they crosslink the polyurethane and form a more rigid polymer. The amount of such ure- thane crosslinking agents is generally from about 1 to about 15 and preferably from about 3 to about 10 parts by weight based upon every 100 parts by weight of the polyurethane.

Flatting agents are added to lower the gloss of the coat- ing surface. The flatting agent migrates to the surface of the coating as the coating is dried. This produces a rough surface that randomly scatters reflected light, which creates a matte appearance.

Important considerations for selection of a flatting agent are particle size distribution, rheological effects, color/clarity, ease of

dispersion and good suspension in coating solution. Typically, flatting agents are particulate materials with average particle sizes in the range of 3-12 microns. Examples of flattening agents include various urea-formaldehydes, various silicas such as precipated silica and fumed silica, talc, alumina, or calcium carbonate, and the like.

Examples of suitable urea-formaldehyde flattening agents include Pergopak M3 (mean particle size 5-7p), from Lonza of New Jersey. Examples of suitable silica flattening agents include Syloid 7000, Syloid C-907 (a synthetic amorphacylica wherein the surface is treated with a hydrocarbon-type wax) from W. R. Grace of Maryland.

The amount of such flattening agents will depend on the amount of initial gloss and the desired flatness desired. Generally speaking, the amount of such flattening agents is from about 0.1 to about 40 parts by weight, and preferably from about 0.5 to about 10 parts by weight based upon the total weight of the polyurethane and the polyvinyl es- ter forming monomers or oligomers.

Waxes are added to increase scratch and mar resistance.

They also have an added effect of lowering gloss. Important proper- ties for wax selection include particle-size distribution, hardness, melt- ing temperature, and ease of dispersion. Such waxes include polyeth- ylene wax such as micronized polyethylene wax, micronized propylene wax, micronized fluorocarbon wax, PTFE wax, or polyol ether ester wax, and the like. Polyethylene and PTFE waxes provide the best combination of toughness and lubrication for scratch and mar resis- tance. Such waxes are commercially available as PolyFlo 190 (a mi- cronized fluorocarbon having a mean particle size of 10 to 12 microns, and Syn Flo 180XF (a synthetic wax and PTFE having a mean particle size of from 3 to 5 microns), and MPD-611 (a micronized polyethylene wax having a mean particle size of from 6 to 8 microns. A preferred wax is a polyethylene wax such as Shamrock Neptune 1 N1 from

Shamrock. The amount of such scratch and mar resistant agents will depend upon the desired resistance and generally is from about 0.1 to about 20 parts by weight and preferably from about 0.3 to about 10 parts by weight for every 100 parts by weight of the polyurethane and the polyvinyl ester forming monomers or oligomers.

Wetting agents are utilized to aid leveling of the coating and mixing of other components. Examples of suitable wetting agents include polydimethylsiloxanes such as BYK 330,333, and 325 from BYK Chemie, alkyl sulfonates, polyethylenes such as S-379 and S-400 from Shamrock, polypropylenes, polytetrafluroethylenes (PTFE), Car- nouba Wax such as S-3015 from Shamrock, and the like. The amount of such wetting agents can vary but generally is from about 0.1 to about 10 or 15, and preferably from about 0.1 to about 2.0 parts by weight for every 100 parts by weight of the polyurethane and the polyvinyl ester forming monomers or oligomers.

Initially, the waterborne polyurethane is mixed with the free radical polymerizable monomers and oligomers with a suitable amount of initiators. At this point, the various optional additives can be added such as a urethane crosslinking agent, a scratch resistance agent, a mar resistance agent, a flattening agent, a wetting agent, and the like. The aqueous mixture is then applied to a substrate and sub- jected to heat to drive off essentially all of the water. The substrate can be any desirable compound and preferably is in the form of a sheet or a film such as plastic, for example polyester, nylon, polyole- fin, and the like with polyvinyl chloride, either rigid or flexible being preferred. Other suitable substrates include various metals, paper, and the like. One suitable method includes applying a portion of the waterborne polyurethane-polyacid monomer mixture by roll coating the substrate or by utilizing a gravure method. The waterborne urethane- free radical polymerizable monomer mixture, etc. can be heated to any suitable temperature to drive the water off at a temperature of from

about 130°F to about 200°F. As the aqueous mixture is conveyed through an oven, the water is gradually removed with a coating sheet or a film being formed on the substrate. Thus, a laminate is formed.

The coating will contain the various optional additives as well as the free radical polymerizable monomers and oligomer and photoinitiators. The sheet or film layer on the substate is then sub- jected to UV light in any suitable manner as being conveyed there- under, conveyed to a suitable container such as an oven wherein an appropriate source of UV lighting is applied, or the like. The intensity and wavelength of the UV light is sufficient to initiate free radical po- lymerization of the monomers and oligomers polymerized the same.

For example, the free radical polymerization can be initiated with a mercury vapor lamp which emits UV light over a wavelength range of 200-450nm. Typical light intensities from Hg vapor lamps are given below.

A band (390nm-320nm)-600 to 200 mW/cm2 B band (320nm-280nm)-500 to 1 75 mW/cm2 C band (260nm-250nm)-75 to 20 mW/cm2 UV sources with higher intensities can also be used.

While the exact co-mingled polyurethane-polyvinyl ester, (e. g. polyacrylate) composition is not known, and not being bound thereto, it is thought that it can be a physical blend of the polyure- thane and polyvinyl ester, or it can be an interpenetrating polymer blend thereof, or it can be a partially crosslinked system between the polyurethane and the polyvinyl ester, or any combination thereof, or one or more other types of compositions.

Regardless of the exact nature of the composition, such co-mingled polyurethane-polyvinyl ester polymer composition in the form of a sheet or film, on a substrate, i. e. a laminate, can be utilized in a variety of end use items. One desired end use application is as a coating for various products or end use items. Suitable products in-

clude desks, tables, or cabinet doors, wall covering, wood, or counter- tops. To form the coating, the laminate is adhered to the product with a suitable adhesive. Suitable adhesives include urethane, ethyl- ene vinyl acetate, and epoxy based resins. The same can also be ac- complished by a variety of other methods. One such method is simply to apply the commingled polyurethane-polyvinyl ester composition di- rectly to the end product or end use item as by spraying or coating the same and then applying radiation as noted herein above to polymerize the vinyl ester monomers or oligomers. Such a method is not pre- ferred. Another method which is desired is a thermoforming process or step in which a vacuum is generally applied to the end product to draw the co-mingled polyurethane-polyvinyl ester polymer composition laminate into contact therewith. Subsequently, or in conjunction therewith, heat is applied to the composition laminate to a suitable temperature to cause the same to adhere to the end product. It is thought that a crosslinked network can result through self-crosslinking as well as grafting of the polyurethane and the polyacid moiedies.

However, the same is not known and accordingly this application is not bound thereto. If the co-mingled polyurethane-polyvinyl ester layer of the laminate contains urethane crosslinking agents therein, once applied to the substrate, it is heated to a sufficient temperature to crosslink the polyurethane. Generally temperatures of from about 220°F to about 450°F and desirably from about 250°F to about 280°F are suitable. Crosslinking, naturally will form a more rigid coating.

The polyurethane generally imparts flexibility to the composition whereas the polyvinyl ester, such as polyacrylate imparts scratch and chemical resistance.

The polyurethane-polyvinyl ester composition can be util- ized for a variety of end uses such as in the formation of hard durable laminates having good scratch resistance, mar resistance, stain resis-

tance, and solvent resistance; non-yellowing properties; low gloss ; anti-static; and the like. Accordingly, suitable end use include lami- nates for desk tops, for bookcases, for table tops, for kitchen cabinets and doors, for electronic devices, molding, and the like, and the same can be made from wood, medium fiberboard, pressboard, plywood, metal, plastics and the like.

The present invention will be better understood by refer- ence to the following examples, which serve to illustrate, but not to limit the invention.

EXAMPLES Examples 1-4 Sample Preparation The waterbase/UV hybrid coatings presented in this disclosure were prepared from the following formulations. Zeneca Sartomer Irgacure Zeneca 9603 9035 500 CX100 Waterborne aliphatic 100 parts urethane polymer Waterborne aliphatic 100 parts 2 parts urethanepolymer + Polyaziridine Waterborne aliphatic 100 parts 11.2 parts 0.8 parts urethanepolymer + Ethoxylated Triacrylate Waterborne aliphatic 100 parts 11.2 parts 0.8 parts 2 I urethanepolymer + EthoxylatedTriacrylate + Polyaziridine

Coatings were applied to PVC sheets with a #3 drawdown bar. The applied coatings were dried in a lab oven. Coatings containing UV curable components were passed under the UV lamps in a laboratory UV curing system to form a laminate. The PVC substrate was 0.016 inch thick with a moderately embossed surface.

Drying conditions were as follows : Oven Temperature 1 78OF Oven Time 120 seconds Curing (polymerization) conditions were as follows: UV Curing Two 200 watts/cm lamps Conveyor Speed 30 yars/min Approximate Dosage 90 mJ/cm2 (250-260 nm) The physical testing was carried out on coated PVC films (laminate) before and after thermoforming in the Greco membrane press. The press cycle (thermoforming) is described below.

1. Coated PVC (laminate) is placed over a MDF board 2. Flexible membrane is laid over laminate and MDF board 3. The membrane is heated to 305-310°F.

4. A vacuum pulls the membrane tightly around the laminate and MDF board (thermoforming). Heat is maintained for 1 minute.

5. Heat is removed and membrane is allowed to cool for 1 minute while vacuum is maintained 6. After 1 minute cooling, vacuum is released and sample is removed.

7. Maximum surface temperature of PVC is measured and recorded with a temperature indicating tape. The target temperature was 180°F.

The following test procedures were used to measure coating durability Scratch Resistance Scratch resistance was measured with a"Balance Beam Scrape Ad- hesion and Mar Tester"that is manufactured by the Paul N. Gardner Company, Inc.. A Hoffman stylus was used to scratch the coatings.

The scratch resistance given in the table above is the high stylus load the coating can withstand with out scratching.

Burnish Mar Mar resistance was determined by firmly rubbing a polished porcelain pestle on the coating surface. The severity of a mark is visually as- sesses as Moderate, Slight or None.

Solvent Resistance (MEK double wipes) A cloth towel was soaked with MEK and gently rubbed on the coated surface in a back and forth manner. One back and forth movement was counted as one wipe. The coated surface was wiped until a break in the coating surface first became visible.

Coating Crack After thermoforming the coated PVC films to molded MDF parts, the corners and edges were visually inspected for coating cracks.

Discussion of Results Physical test results are given in Table 1.

Addition of the ethoxylated triacrylate to the waterborne ali- phatic urethane dispersion resulted in improved scratch and mar resistance. The results also show an improvement in scratch and mar resistance after thermoforming.

The ethoxylated triacrylate produced a greater increase in scratch and mar resistance than the thermal crosslinker, polyaziridine. However, the best scratch and mar resistance is obtained with a combination of ethoxylated triacrylate and polyaziridine.

Addition of the ethoxylated triacrylate resulted in a modest in- crease in solvent resistance.

- Table l : Durability Test results from UV/Waterbase Hybrid Coatings Coating Thermo-Scratch Burnish MEK Coating formed Resistance Mar Double Crack (g) Wipes Example 1 No 1900 Moderate 11 Waterborne aliphatic urethane polymer Yes 2100 Moderate 24 None (Zeneca 9603) Example 2 No 2200 Moderate 12---- Waterbornealiphatic urethanepolymer (Zeneca 9603) Yes 2800 Moderate-17 None + Slight Polyaziridine (CX100) . F Q, R b, :-S u f j, Example3 No 2500 Moderate-20---- Waterborne aliphatic None urethane polymer (Zeneca 9603) (Zeneca3200 Slight-21 None Ethoxylated Triacrylate (Sartomer 9035) Example4 No 3000 Slight-22 Waterborne aliphatic i urethane polymer (Zeneca 9603) + EthoxylatedYes 3500 None 21 None Triacrylate (Sartomer 9035) + Polyaziridine (CX100)

Examples 5-9 Low Gloss Waterborne/UV Hybrid Coating for Paper and Plastic Decorative Laminate The disclosed coating describes a waterborne/UV hybrid coating for thermoformable vinyl laminates. These laminates are widely used as thermoformable foils for molded substrates. A com- mon example of this application is kitchen cabinet doors.

Flattening agents are often added to protective coatings to produce a low gloss appearance. The following example describes the effect of flatting agents and polyethylene wax to the durability of waterborne/UV hybrid coatings.

Sample Preparation The waterborne/UV hybrid coatings presented in this disclosure were prepared from the following formulations. Nm c- Z l ? cn a C m m m cn < to 0 0 CD cn CD (D N s - § . g ? . "Oj'-TO' (6 fC-t tQC)'C.. ( ?- 5'TOOrr2082 a ° :- . tn cn' o °'-. o d m o ce a o > > Z ' o °,-' i GJ 'O m cD cp GJ 5 100 11. 2 0. 8 2 6 87. 75 10 0. 75 3 3 7 87.75 10 0.75 3 3 8 87. 75 10 0. 75 3 1 987. 75100. 75311

Coats were applied to PVC sheets in a manner as described hereinabove with regard to Examples 1 through 4. Similarly, the same tests and test procedures were utilized. The results of the test were as follows : Testing Results Examples 5 to 9: Durability Test results from Low Gloss UV/Waterborne Hybrid Coatings Thermo-Scratch Burnish Coating Gloss formed Resistance Mar Crack % (g) Example 5: No 3000 Slight-None----44 No flatting agent orpolyethylene Yes 3500 None None wax Example6 : No 1800 Moderate----10 Syloid 7000 Yes 1900 Moderate None Example 7 : No 1400 Moderate----9 l I Pergopak M3 Yes 1300 Moderate None I Example 8: No 2500 Moderate----11 Syloid 7000 + Yes 3000 Moderate None Neptune1N1 D X E S T = f X Example 9: No 2700 Slight----11 Pergopak M3 + Yes 4500 Slight-None Neptune 1N1 Moderate

As apparent from the above data, none of the coatings cracked after thermoforming. Moreover, Examples 6 through 9, which contained flattening agents contained good gloss reduction.

While in accordance with the patent statutes the best mode and preferred embodiment has been set forth, the scope of the invention is not limited thereto, but rather by the scope of the attached claims.