Patent Application
20180327606
Embodiments of the present invention relate to a stain resistant coating for flooring tiles and panels, methods for preparing and applying the stain resistant coating, and flooring systems comprising the abrasion resistant coating.
Heretofore, curable coating compositions have been used as overcoat materials to cover the surface of flooring products or various stain heavy surfaces to protect such a products or surfaces from tarnish by stain or dirt. Although there have been previous attempts at creating stain resistant coatings, there remains a need to provide a stain resistant flooring products that are not only dirt and stain resistant, but also have desirable attributes of conventional flooring products such as conventional maintenance attributes.
Embodiments of the present invention are directed to a floor covering comprising: a substrate, and a coating layer comprising a cross-linked polymer formed from a curable coating composition comprising an acrylate-functional resin; wherein the cross-linked polymer has a glass transition temperature equal to or greater than room temperature and has a cross-link density of at least about 0.0035 C═C eq/gm as measured from the polymerization of carbon-carbon double bonds in the curable coating composition.
Other embodiments of the present invention are directed to a floor covering comprising: a substrate, and a coating layer comprising a cross-linked polymer formed from a curable coating composition comprising a mixture of: an acrylate-functional polymeric resin; an acrylate-functional oligomer having an acrylate-functionality ranging from two to four; wherein the cross-linked polymer has a glass transition temperature of at least about 40° C. and has a cross-link density of at least about 0.004 C═C eq/gm as measured from the polymerization of carbon-carbon double bonds in the curable coating composition.
Other embodiments of the present invention are directed to a method of forming a floor covering comprising: mixing together an acrylate polymeric resin, a di-functional acrylate oligomer, and a tri-functional acrylate oligomer to form a curable coating composition; applying the curable coating composition to a top surface of a substrate; exposing the curable coating composition to form a cross-linked coating layer; wherein the cross-linked coating layer has a glass transition temperature of at least about 30° C. and has a cross-link density of at least about 0.0035 C═C eq/gm as measured from the polymerization of carbon-carbon double bonds in the curable coating composition.
The present invention is directed to floor coverings comprising a substrate and a stain resistant coating layer (also referred to as “coating layer”). The coating layer may comprise a cross-linked polymer and optionally a matting agent. The coating layer may further comprise abrasion resistant particles. The cross-linked polymer may be formed from a curable coating composition curable coating composition that comprises a blend of acrylate-functional compounds—such as acrylate-functional polymeric resin, acrylate-functional oligomer, acrylate-functional monomer, and combinations thereof.
Acrylate-functional polymeric resin that may be used in the curable coating composition to form the cross-linked polymer may include acrylate functional polyester (as referred to as “polyester acrylate”), acrylate functional polyurethane (as referred to as “polyurethane acrylate”), acrylate functional polyether (as referred to as “polyether acrylate”), acrylate functional polysiloxane (as referred to as “polysiloxane acrylate”), acrylate functional polyolefin (as referred to as “polyolefin acrylate”), as well as blends and copolymers thereof.
The acrylate-functional polymeric resin may include a linear or branched polymer having at least one acrylate or (meth)acrylate functional group. In some embodiments, the polymer of the acrylate functional polymeric resin may comprise an acrylate groups, methacrylate groups, or a combination thereof. According to the present invention, the term “acrylate” may also refer methacrylate groups. The acrylate-functional polymer of the present invention may have between 1 to 10 free acrylate groups, methacrylate groups, or a combination thereof—including all values and sub-ranges there-between. The acrylate-functional polymeric resin may be present in an amount ranging from about 25 wt. % to about 55 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
The acrylate-functional polyester may be the reaction product of polyester polyol and an carboxylic acid functional acrylate compound such as acrylic acid, (meth)acrylic acid, or a combination thereof at a OH:COOH ratio of about 1:1. The polyester polyol may be a polyester diol having two hydroxyl groups present at terminal end of the polyester chain. In some embodiments, the polyester polyol may have a hydroxyl functionality ranging from 3 to 9, wherein the free hydroxyl groups are present at the terminal ends of the polyester chain or along the backbone of the polyester chain.
In non-limiting embodiments, the polyester polyol may be the reaction product of a hydroxyl-functional compound and a carboxylic acid functional compound. The hydroxyl-functional compound is present in a stoichiometric excess to the carboxylic-acid compound. In some embodiments the hydroxyl-functional compound is a polyol, such a diol or a tri-functional or higher polyol (e.g. triol, tetrol, etc.). In some embodiments the polyol may be aromatic, cycloaliphatic, aliphatic, or a combination thereof. In some embodiments the carboxylic acid-functional compound is dicarboxylic acid, a polycarboxylic acid, or a combination thereof. In some embodiments, the dicarboxylic acid and polycarboxylic acid may be aliphatic, cycloaliphatic, aromatic, or a combination thereof.
In some embodiments the diol may be selected from alkylene glycols, such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol, tripropylene glycol, hexylene glycol, polyethylene glycol, polypropylene glycol and neopentyl glycol; hydrogenated bisphenol A; cyclohexanediol; propanediols including 1,2-propanediol, 1,3-propanediol, butyl ethyl propanediol, 2-methyl-1,3-propanediol, and 2-ethyl-2-butyl-1,3-propanediol; butanediols including 1,4-butanediol, 1,3-butanediol, and 2-ethyl-1,4-butanediol; pentanediols including trimethyl pentanediol and 2-methylpentanediol; cyclohexanedimethanol; hexanediols including 1,6-hexanediol; caprolactonediol (for example, the reaction product of epsilon-caprolactone and ethylene glycol); hydroxy-alkylated bisphenols; polyether glycols, for example, poly(oxytetramethylene) glycol. In some embodiments, the tri-functional or higher polyol may be selected from trimethylol propane, pentaerythritol, di-pentaerythritol, trimethylol ethane, trimethylol butane, dimethylol cyclohexane, glycerol and the like.
In some embodiments the dicarboxylic acid may be selected from adipic acid, azelaic acid, sebacic acid, succinic acid, glutaric acid, decanoic diacid, dodecanoic diacid, phthalic acid, isophthalic acid, 5-tert-butylisophthalic acid, retrahydrophthalic acid, terephthalic acid, hexahydrophthalic acid, methylhexahydrophthalic acid, dimethyl terephthalate, 2,5-furandicarboxylic acid, 2,3-furandicarboxylic acid, 2,4-furandicarboxylic acid, 3.4-furandicarboxylic acid, 2,3,5-furantricarboxylic acid, 2,3,4,5-furantetracarboxylic acid, cyclohexane dicarboxylic acid, chlorendic anhydride, 1,3-cyclohexane dicarboxylic acid, 1,4-cyclohexane dicarboxylic acid, and anhydrides thereof, and mixtures thereof. In some embodiments the polycarboxylic acid may be selected from trimellitic acid and anhydrides thereof.
The acrylate-functional polyester may have between 1 to 10 free acrylate groups, methacrylate groups, or a combination thereof—including all values and sub-ranges there-between.
The acrylate-functional polyurethane according to the present invention may be a linear or branched polymer having at least one functional group selected from an acrylate group or a (meth)acrylate group. In some embodiments, the acrylate-functional polyurethane may has at least 2 to 9 functional groups selected from an acrylate group, a (meth)acrylate group, or a combination thereof. In some embodiments, the acrylate-functional polyurethane has between 2 and 4 functional groups selected from an acrylate group, (meth)acrylate group, or a combination thereof.
In some embodiments, the acrylate functional polyurethane may be the reaction product of a high molecular weight polyol and diisocyanate, polyisocyanate, or a combination thereof. The high molecular weight polyol may be selected from polyester polyol, polyether polyol, polyolefin polyol, and a combination thereof—the high molecular weight polyol having a hydroxyl functionality ranging from 2 to 9.
The polyester polyol used to create the acrylate-functional polyurethane may be the same as the polyester polyol that is used to form the acrylate functional polyester. In some embodiments, the polyether polyol may be selected from polyethylene oxide, polypropylene oxide, polytetrahydrofuran, and mixtures and copolymers thereof.
The high molecular weight polyol may be reacted with polyisocyanate, such as a diisocyanate, a tri-functional isocyanate (e.g. isocyanurate), higher functional polyisocyanates, or a combination thereof in an NCO:OH ratio ranging from about 2:1 to 4:1. The polyisocyanate may be selected from isophorone diisocyanate, 4,4′-dicyclohexylmethane-diisocyanate, and trimethyl-hexamethylene-diisocyanate, 1,6 hexamethylene diisocyanate, 2,2,4-trimethylhexamethylenc diisocyanate, octadecylene diisocyanate and 1,4 cyclohexylene diisocyanate, toluene diisocyanate; methylenediphenyl diisocyanate: tetra methylxylene diisocyanate, and isocyanurates (“trimmers”), biurets (“dimers”), allophanates thereof, as well as mixtures thereof. The resulting reaction product is an isocyanate-terminated prepolymer.
The isocyanate-terminated prepolymer is then reacted with hydroxyl-functional acrylate compound in an NCO:OH ratio of about 1:1 to yield an acrylate or (meth)acrylate functional polyurethane. The hydroxyl-functional acrylate compounds may include hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate, hydroxypentyl acrylate, hydroxypentyl methacrylate, hydroxyhexyl acrylate, hydroxyhexyl methacrylate, aminoethyl acrylate, and aminoethyl methacrylate, and a combination thereof.
The acrylate-functional polyurethane may have between 1 to 10 free acrylate groups, methacrylate groups, or a combination thereof—including all values and sub-ranges there-between.
The curable coating composition of the present invention may further comprise acrylate-functional oligomer or monomer—that may include at least one of mono-functional monomer and/or oligomer (i.e., having an acrylate functionality of one), di-functional oligomers (i.e., having an acrylate functionality of two), tri-functional oligomers (i.e., having an acrylate functionality of three), tetra-functional oligomers (i.e., having an acrylate functionality of four, penta-functional oligomers (i.e., having an acrylate functionality of five), and combinations thereof.
Non-limiting examples of di-functional oligomer include ethylene glycol diacrylate, propylene glycol diacrylate, diethylene glycol diacrylate, dipropylene glycol diacrylate, triethylene glycol diacrylate, tripropylene glycol diacrylate, polyethylene glycol diacrylate, polypropylene glycol diacrylate, ethoxylated bisphenol A diacrylate, bisphenol A diglycidyl ether diacrylate, resorcinol diglycidyl ether diacrylate, 1,3-propanediol diacrylate, 1,4-butanediol diacrylate, 1,5-pentanediol diacrylate, 1,6-hexanediol diacrylate, neopentyl glycol diacrylate, cyclohexane dimethanol diacrylate, ethoxylated neopentyl glycol diacrylate, propoxylated neopentyl glycol diacrylate, ethoxylated cyclohexanedimethanol diacrylate, propoxylated cyclohexanedimethanol diacrylate, and mixtures thereof.
The di-functional oligomer may be present in an amount ranging from about 10 wt. % to about 30 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
Non-limiting examples of tri-functional oligomers include trimethylol propane triacrylate, isocyanurate triacrylate, glycerol triacrylate, ethoxylated trimethylolpropane triacrylate, propoxylated trimethylolpropane triacrylate, tris (2-hydroxyethyl) isocyanurate triacrylate, ethoxylated glycerol triacrylate, propoxylated glycerol triacrylate, pentaerythritol triacrylate, melamine triacrylates, and mixtures thereof.
The tri-functional oligomer may be present in an amount ranging from about 2 wt. % to about 15 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
Non-limiting examples of tetra-functional oligomers may include di-trimethylolpropane tetraacrylate, pentaerythritol tetraacrylate, alkoxylated pentaerythritol tetraacrylate, di-pentaerythritol tetraacrylate, alkoxylated dipentaerythritol tetraacrylate, and combinations thereof. The alkoxylation may be performed using ethylene oxide, propylene oxide, butylene oxide, or mixtures thereof. In some embodiments the degree of alkoxylation ranges from about 2 to 10. In some embodiments, the degree of alkoxylation ranges from about 4 to 6.
The tetra-functional oligomer may be present in an amount ranging from about 0 wt. % to about 10 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
Non-limiting examples of acrylate functional monomers include alkyl acrylates having up to about 12 carbon atoms in the alkyl segment such as ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, amyl acrylate, n-lauryl acrylate, nonyl acrylate, n-octyl acrylate, isooctyl acrylate, isodecyl acrylate, etc.; alkoxyalkyl acrylates such as methoxybutyl acrylate, ethoxyethyl acrylate, ethoxypropyl acrylate, etc.; hydroxyalkyl acrylates such as hydroxyethyl acrylate, hydroxybutyl acrylate, etc.; alkenyl acrylates such as trimethoxyallyloxymethyl acrylate, allyl acrylate, etc.; aralkyl acrylates such as phenoxyethyl acrylate, benzyl acrylate, etc.; cycloalkyl acrylates such as cyclohexyl acrylate, cyclopentyl acrylate, isobornyl acrylate, etc.; aminoalkyl acrylates such as diethylaminoethyl acrylate; cyanoalkyl acrylates such as cyanoethyl acrylate, cyanopropyl acrylate, etc.; carbamoyloxy alkyl acrylates such as 2-carbamoyloxyethyl acrylate, 2-carbamoyl-oxypropyl acrylate, N-methylcarbamoyloxyethyl acrylate, N-ethylcarbamoyloxymethyl acrylate, 2-(N-methylcarbamoyloxy)-ethyl acrylate, 2-(N-ethylcarbamoyloxy)ethyl acrylate, etc.; and the corresponding methacrylates. In some embodiments, the alkyl acrylates having up to about 12 carbon atoms in the alkyl segment may be used as a reactive solvent/diluent in the abrasions resistant coating layer. Other non-limiting examples of acrylate-functional monomer may include acrylic acid, methacrylic acid, ethyl acrylic acid, 2-phenoxyethyl acrylate; 2-phenoxyethyl methylacrylate; 2-phenoxyethyl ethylacrylate; tridecryl acrylate; tridecryl methylacrylate; tridecryl ethylacrylate; and mixtures thereof.
Non-limiting examples of the mono-functional oligomers include alkoxylated tetrahydrofurfuryl acrylate; alkoxylated tetrahydrofurfuryl methylacrylate; alkoxylated tetrahydrofurfuryl ethylacrylate; alkoxylated phenol acrylate; alkoxylated phenol methylacrylate; alkoxylated phenol ethylacrylate; alkoxylated nonylphenol acrylate; alkoxylated nonylphenol methylacrylate; alkoxylated nonylphenol ethylacrylate, and mixtures thereof. The alkoxylation may be performed using ethylene oxide, propylene oxide, butylene oxide, or mixtures thereof. In some embodiments the degree of alkoxylation ranges from about 2 to 10. In some embodiments, the degree of alkoxylation ranges from about 4 to 6.
The acrylate-functional monomer or oligomer may further comprise an acrylate-functional silicon containing composition—such as a siloxane. Curable silicone acrylates are known and suitable silicone acrylates are disclosed, for example in U.S. Pat. No. 4,528,081 and U.S. Pat. No. 4,348,454. Suitable silicone acrylates include silicone acrylates having mono-, di-, and tri-acrylate moieties. Suitable silicone acrylates include, for example, Silcolease® UV RCA 170 and UV Poly 110, available from Blue Star Co. Ltd, China; and Silmer ACR D2, Silmer ACR Di-10, Silmer ACR Di-50 and Silmer ACR Di-100, available from Siltech.
The mono-functional monomer and/or oligomer may be present in an amount ranging from about 5 wt. % to about 25 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition. The silicone acrylate in particular may be present in an amount ranging from about 0 wt. % to 6 wt. % based on the total weight of the curable coating composition. In some embodiments, the silicone acrylate may be present in an amount ranging from about 1 wt. % to 5 wt. % based on the total weight of the curable coating composition. In some embodiments, the silicone acrylate may be present in an amount ranging from about 1 wt. % to 3.5 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
The curable coating composition may further comprise photoinitiator to help facilitate the cross-linking of the curable coating composition. Non-limiting examples of photoinitiator may include a benzoin compound, an acetophenone compound, an acylphosphine oxide compound, a titanocene compound, a thioxanthone compound or a peroxide compound, or a photosensitizer such as an amine or a quinone. Specific examples photoinitiatiors include 1-hydroxycyclohexyl phenyl ketone, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzyl diphenyl sulfide, tetramethylthiuram monosulfide, azobisisobutyronitrile, dibenzyl, diacetyl and beta-chloroanthraquinone. In some embodiments, the photoinitiators are water soluble alkylphenone photoinitiators.
The curable coating composition may further comprise an amine synergist. Non-limiting examples of amine synergist may include diethylaminoethyle methacrylate, dimethylaminoethyl methacrylate, N—N-bis(2-hydroxyethyl)-P-toluidine, Ethyl-4-dimethylamino benzoate, 2-Ethylhexyl 4-dimethylamino benzoate, as well as commercially available amine synergist, including Sartomer CN 371, CN373, CN383, CN384 and CN386; Allnex Ebecry P104 and Ebecry P115. The amine synergist may be present in an amount ranging from about 1 wt. % to about 5 wt. %, preferably about 3 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
The curable coating composition may optionally further comprise other additives and fillers, such as abrasives, surfactant, abrasion resistant particles, pigments, tackifiers, matting agents, surfactant, fillers such as glass or polymeric bubbles or beads (which may be expanded or unexpanded), hydrophobic or hydrophilic silica, calcium carbonate, glass or synthetic fibers, blowing agents, toughening agents, reinforcing agents, fire retardants, antioxidants, and stabilizers. The additives are added in amounts sufficient to obtain the desired end properties.
Non-limiting examples of abrasion resistant particles may include particles of carborundum, quartz, silica, silicon carbide, diamond, aluminum oxide (alumina) having a particle size ranging from about 1 micron to about 30 micron—including all values and sub-ranges there-between. The abrasion resistant particles may be present in an amount ranging from about 0 wt. % to about 20 wt. %—including all values and sub-ranges there-between.
Suitable surfactants of the present invention include, but are not limited to, fluorinated alkyl esters, polyether modified polydimethylsiloxanes and fluorosurfactants, having the formula R1CH2CH2O(CH2CH2O)xH, wherein R1═F(CF2CF2)y, x=0 to about 15, and y=1 to about 7. The surfactant may be present in an amount ranging from about 0.5 wt. % to about 2 wt. %, preferably about 0.8 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
In some embodiments, the matting agent may comprise small particles of polyamide, fluoropolymer, silica, and combinations thereof. In some non-limiting embodiments, the polyamide powder may have a melting point up to 142° C. and a particle size ranging from about 8 μm to 12 μm; preferably 10 μm. The polyamide powder may be polyamide-6,6, polyamide-6.9; polyamide-6, 10; polyamide-6, 12; and polyamide-12:6/12—preferably polyamide-6,12. The polyamide powder may be present in amount ranging from 5 wt. % to 10 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
The curable coating composition may further comprise particles formed from a fluoro-carbon composition. The fluoro-carbon composition may function as a matting agent in the curable coating composition and resulting cross-linked polymer. The fluoro-carbon composition may comprise fluoropolymer—such as a fluoropolymer wax—which may be optionally blended with one or more polyolefin waxes. Suitable fluoropolymer waxes may have an average particle size ranging from about 0.5 μm to 30 μm, preferably from about 1 μm to 15 μm. The fluoropolymer waxes may be selected from polytetrafluoroethylene (PTFE), fluorinated ethylene propylene (FEP), perfluoroalkoxy polymer resin (PFA), ethylene tetrafluoroethylene (ETFE), ethylene chloro trifluoroethylene (ECTFE), polychlorotrifluoroethylene (PCTFE), polyvinylidene fluoride (PVDF), and combinations thereof. In some embodiments, the fluoropolymer is PTFE. Suitable polyolefin waxes may include polyethylene waxes and polypropylene waxes. The fluoro-carbon composition may comprise about 10 wt. % to about 90 wt. % of fluoropolymer wax and about 10 wt. % to about 90 wt. % of polyolefin wax—including all values and sub-ranges there-between. In some embodiments, the fluoro-carbon composition may comprise about 20 wt. % to about 30 wt. % of fluoropolymer wax and about 70 wt. % and 80 wt. % of polyolefin wax.
The fluoro-carbon composition may be present in an amount ranging from about 0 wt. % to 5 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition. In some embodiments, the fluoro-carbon composition may be present in an amount ranging from about 1 wt. % to 3.5 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition.
The amount of the silicon acrylate and the fluoropolymer may sum to a total that ranges from about 0 wt. % to about 5 wt. %—including all values and sub-ranges there-between—based on the total weight of the curable coating composition. The silicon acrylate may be present relative to the fluoropolymer in a weight ratio ranging from about 2:1 to 1:2—including all ratios and sub-ranges there-between—including 1:1.
In some embodiments, the silica may have a particle size at d50 (50% distribution) ranging from about 3 μm to 7 μm—including all values and sub-ranges there-between (including 5 μm)—based on the total weight of the curable coating composition. The silica may be present in amount ranging from 1 wt. % to 3 wt. %—including all values and sub-ranges there-between (including 5 μm)—based on the total weight of the curable coating composition.
The cross-linked polymer may be formed by applying the curable coating composition to an upper surface of a substrate and exposing the curable coating composition to UV radiation (as discussed further herein). The resulting cross-linked polymer may have a glass transition (Tg) temperature equal to or greater than room temperature (i.e., about 20-23° C.). The cross-linked polymer may have a glass transition temperature that is equal to greater than 20° C.—preferably at least about 25° C. to about 70° C.—including all values and sub-ranges there-between.
The cross-linked polymer that is formed from the curable coating composition of the present invention will have a degree of cross-linking that may depend upon the amount and frequency of pendent double bonds in each of the acrylate-functional compounds present in the curable coating composition. Specifically, the degree of cross-linking may change in the resulting cross-linked polymer depending on the relative amounts of mono, di, tri, tetra, and/or penta-functional acrylate monomer, oligomer and/or polymeric resin. As the functionality of each acrylate-functional compound increases in the curable coating composition, there is a corresponding increase in the degree of cross-linking in the resulting cross-linked polymer as there are more covalent bonds being created between reactive components. Furthermore, as molecular weight of each acrylate-functional compound decreases, there may be a corresponding increase in the degree of cross-linking in the resulting cross-linked polymer as the reduction in molecular weight in reactive compounds creates a corresponding increase in the frequency between covalent bonds between functional groups—thereby increasing cross-link density.
According to the present invention, the di-functional oligomer may be present relative to the tri-functional oligomer in a weight ratio ranging from about 5:1 to about 2:1—including all ratios and sub-ranges there-between. According to the present invention, the di-functional oligomer may be present relative to the tetra-functional oligomer in a weight ratio ranging from about 6:1 to about 4:1—including all ratios and sub-ranges there-between. According to the present invention, the tri-functional oligomer may be present relative to the tetra-functional oligomer in a weight ratio ranging from about 2:1 to about 3:1—including all ratios and sub-ranges there-between. According to the present invention, the di-functional oligomer may be present relative to the mono-functional oligomer/monomer in a weight ratio ranging from about 1.5:1 to about 2:1—including all ratios and sub-ranges there-between. According to the present invention, the tri-functional oligomer may be present relative to the mono-functional oligomer/monomer in a weight ratio ranging from about 1:2 to about 1:4—including all ratios and sub-ranges there-between.
For the purpose of the present invention, cross-link density may be measured as the number of equivalent carbon-carbon bonds (also referred to as “C═C” bonds) created in the cross-linked polymer per unit of mass of the cross-linked polymer—i.e. C═C eq/gm. The cross-link density of the cross-linked polymer of the present invention may be at least about 0.0035 C═C eq/gm. The cross-link density of the cross-linked polymer of the present invention may range from about 0.0035 C═C eq/gm to about 0.005 C═C eq/gm—including all values and sub-ranges there-between.
The floor covering of the present invention comprises a substrate covered with the coating layer of the present invention, wherein the coating layer comprises the cross-linked polymer having a glass transition temperature of at least 35° C. up to about 55° C. and a cross-link density of at least about 0.0035 C═C eq/gm up to about 0.005 C═C eq/gm. The cross-linked polymer may be present in the coating layer in an amount ranging from about 65 wt. % to about 99 wt. %—including all values and sub-ranges there-between—preferably from about 75 wt. % to about 85 wt. %—including all values and sub-ranges there-between. The resulting coating layer—which comprises the cross-linked polymer—exhibits superior stain resistance and cleanability as well as superior scratch, scuff, and stain resistance while also being able to sufficiently bond to the underlying substrates. Thus, the resulting floor covering comprising a substrate and the coating layer of the present invention provides a superior flooring product as the top surface can be easily cleaned and kept aesthetically pleasing during prolonged while also maintaining the necessary bond strength necessary to keep the coating layer bonded to the substrate, thereby maintaining the floor covering intact as single multi-layered structure that can withstand the mechanical stress applied during normal use as a flooring material.
Furthermore, while the coating layer of the present invention may include silicon and/or fluoro-carbon containing compounds (which may help cleanability)—including those that may be covalently bonded to the cross-linked polymer—in some embodiments the coating layer may be substantially free of the silicon and/or the fluoro-carbon containing compounds and still achieve the same, it not better, desired cleanability on the top surface of the floor covering.
The coating layer may be formed by the following methodology. The acrylate-functional compounds may be first combined and mixed together at room temperature with high speed agitation. For the purposes of the present application the term high speed agitation means agitation with a blade at rotation speeds of at least 2,000 RPM. A dispersing agent may be added concurrently with the binder components or after the binder components have been blended together. The dispersing agents may be selected from acrylic block-copolymers, such as commercially available BYK Disperbyk 2008, Disperbyk 2155, Disperbyk 145 and Disperbyk 185, Lubrizol Solsperse 41000 and Solsperse 71000, and may an amount ranging from 0.1 wt. % to 1 wt. % based on the total weight of the curable coating composition—including all values and sub-ranges there-between.
Next, the photoinitiator is slowly added at room temperature. In some alternative embodiments, the photoinitiator may be added at 45° C. with high speed agitation. Once the photoinitiator is entirely dissolved into the master batch mixture, matting agents and the abrasion resistant particles may be added. The matting agent and, if desired, fillers/abrasives are added to the master batch as the final ingredients. The matting agent should be added slowly to avoid a powder layer from forming and floating on top of blend. Once added, the binder, dispersing agent, photoinitiator, and matting agent are mixed with high speed agitation for a period ranging from about 5 to about 15 minutes, preferably about 10 minutes. During the agitations, the blade may be moved up and down to ensure proper mixing of the ingredients in the master batch. The temperature of the master batch may increase during agitation, therefore to prevent premature thermal curing of the binder, the master batch may be cooled during agitation.
The resulting blend is a curable coating composition and may have a viscosity ranging from about 600 to about 1300 cPs at room temperature (74° F.) as measured by a Brookfield Viscometer using spindle #6 at 100 RPM. In some embodiments of the present invention, the viscosity allows the blend to be applied to a substrate by roll coating at room temperature. The substrates may selected from linoleum tile, ceramic tile, natural wood planks, engineered wood planks, vinyl tile—such as luxury vinyl tile (“LVT”), and resilient sheet—such as homogeneous or heterogeneous commercial resilient sheets and residential resilient sheets. After applying the blend to the substrate, the blend is exposed to UV radiation in air or a nitrogen environment.
The UV radiation includes UVA, UVB, UVC, and UVV sources. In some embodiments, the coating layer may be cured in a single or two-stage curing process. Non-limiting examples of UV partial cure radiation include UVA radiation of 0.189 J/cm2; UVB radiation of 0.163 J/cm2; UVC radiation of 0.01 J/cm2; and UVV radiation may be 0.092 J/cm2. The pre-cure temperature may be 30° C.-40° C. and the coating composition may be exposed to the UV radiation at a line speed ranging from about 25 to 75 FPM. Non-limiting examples of UV full cure include UVA radiation of 1.006 J/cm; UVB radiation of 0.886 J/cm2; UVC radiation of 0.126 J/cm2; and UVV radiation may be 0.504 J/cm2. To fully cure, the coating composition may be exposed to the UV radiation at a line speed ranging from about 25 to 75 FPM. The delay between the pre-cure/partial cure and the full cure ranges from about 3 seconds to about 10 seconds. The fully cured coating layer on the substrate forms the floor covering.
The floor covering of the present invention may consist of a single layer of the coating layer on a substrate. In other embodiments, the floor coating of the present invention may be a multi-layer floor covering. The multi-layer floor covering may be produced by first applying a first layer of the curable coating composition on a substrate by any suitable coating method, including roll coating. The first layer may then be partially or fully cured with, for example, UV radiation—forming a base coat. In other embodiments, the base coat may be a pre-existing base coat. Subsequently, a second layer of the coating composition may be applied to the top surface of the first layer by, for example, roll coating, thereby forming a multilayer coated surface. According to some embodiments, the second layer may then be partially or fully cured with UV radiation. One or more of additional coating layers may be applied on the second layer. Once the multilayer coated surface is formed, the multilayer coated surface can be fully cured, if any of the previously applied layers is only partially cured. The term partial curing as used herein refers to curing a coated layer to a non-fluid state (i.e., semi-solid or solid) that may be tacky to the touch.
In some embodiments, each fully cured coating layer may have an average coating thickness that ranges from about 2 μm to about 50 μm. In some embodiments, the fully cured coating layer may have an average coating thickness that ranges from about 4 μm to about 40 μm. In some embodiments, the fully cured coating layer may have an average coating thickness that ranges from about 6 μm to about 20 μm.
The present invention has been disclosed in conjunction with UV curable coating compositions for illustration purposes only, and other curable coating compositions, such as moisture curable urethane coating compositions, 2K urethane coating compositions, epoxy coating compositions and acrylic coating compositions, can be utilized.
The following examples were prepared in accordance with the present invention. The present invention is not limited to the examples described herein.
A variety of coating layers were created and tested. The coating layer of Example 1 was produced according to the following procedure. Example 1 was prepared by first mixing together the following ingredients:
The relative amount of each reactive component can be summarized in Table 1 below. The polymeric acrylate refers to the polyester and urethane acrylates (i, ii). The tri-acrylate refers to the tri-functional acrylate oligomer (iii). The di-acrylate refers to the di-functional acrylate oligomers (iv, v). The mono-acrylate refers to the mono-functional acrylates (vi, vii, viii)
Next 3.09 grams of amine synergist (Sartomer CN 371) and 4.03 grams of photoinitiator were added with high speed agitation until completely dissolved in the mixture. The photoinitiator included 3.22 grams of diphenyl ketone and 0.81 grams of 1-hydroxy-cyclohexyl phenyl ketone. Additional ingredients include 4.1 grams of filler and surfactant—including 3.71 grams of diamond particle having a particle size of about 6 microns. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a LVT substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Example 1 has a Tg of 48.81° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00364 eq/gm.
Example 2 was prepared by first mixing together the following ingredients
The relative amount of each reactive component can be summarized in Table 2 below. The polymeric acrylate refers to the polyester and urethane acrylates (i, ii). The tri-acrylate refers to the tri-functional acrylate oligomer (iii). The di-acrylate refers to the di-functional acrylate oligomers (iv, v). The mono-acrylate refers to the mono-functional acrylates (vi, vii, viii)
Next 3.42 grams of amine synergist and 4.45 grams of photoinitiator were added with high speed agitation until completely dissolved in the mixture. The photoinitiator included 3.56 grams of diphenyl ketone and 0.89 grams of I-hydroxy-cyclohexyl phenyl ketone. Additional ingredient includes 4.1 grams of diamond particle having a particle size of about 6 μm. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Example 2 has a Tg of 47.8° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00436 eq/gm.
Example 3 was prepared by first mixing together the following ingredients
The relative amount of each reactive component can be summarized in Table 3 below. The polymeric acrylate refers to the polyester and urethane acrylates (i, ii). The tri-acrylate refers to the tri-functional acrylate oligomer (iii). The di-acrylate refers to the di-functional acrylate oligomers (iv, v). The mono-acrylate refers to the mono-functional acrylates (vi, vii)
Next 3.46 grams of amine synergist and 4.5 grams of photoinitiator were added with high speed agitation until completely dissolved in the mixture. The photoinitiator included 3.6 grams of diphenyl ketone and 0.9 grams of 1-hydroxy-cyclohexyl phenyl ketone. Additional ingredients include 4.54 grams of filler and surfactant—including 4.15 grams of diamond particle having a particle size of about 6 microns. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Example 3 has a Tg of 48.52° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00405 eq/gm.
Example 4 was prepared by first mixing together the following ingredients
The relative amount of each reactive component can be summarized in Table 4 below. The polymeric acrylate refers to the polyester and urethane acrylates (i, ii). The tri-acrylate refers to the tri-functional acrylate oligomer (iii). The di-acrylate refers to the di-functional acrylate oligomers (iv, v). The mono-acrylate refers to the mono-functional acrylates (vi, vii)
Next 3.38 grams of amine synergist and 4.4 grams of photoinitiator were added with high speed agitation until completely dissolved in the mixture. The photoinitiator included 3.52 grams of diphenyl ketone and 0.88 grams of I-hydroxy-cyclohexyl phenyl ketone. Additional ingredients include 4.45 grams of filler and surfactant—including 4.06 grams of diamond particle having a particle size of about 6 microns. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Example 4 has a Tg of 48.71° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00396 eq/gm.
Example 5 was prepared by first mixing together the following ingredients
The relative amount of each reactive component can be summarized in Table 5 below. The polymeric acrylate refers to the polyester and urethane acrylates (i, ii). The tetra-acrylate refers to the tetra-functional acrylate oligomer (iii). The tri-acrylate refers to the tri-functional acrylate oligomers (iv, v). The di-acrylate refers to the di-functional acrylate oligomers (vi, vii). The mono-acrylate refers to the mono-functional acrylates (viii, ix)
Next 3.46 grams of amine synergist and 4.5 grams of photoinitiator were added with high speed agitation until completely dissolved in the mixture. The photoinitiator included 3.6 grams of diphenyl ketone and 0.9 grams of 1-hydroxy-cyclohexyl phenyl ketone. Additional ingredients include 4.54 grams of filler and surfactant—including 4.15 grams of diamond particle having a particle size of about 6 microns. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Example 5 has a Tg of 48.71° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00462 eq/gm.
Example 6 was prepared by first mixing together the following ingredients
The relative amount of each reactive component can be summarized in Table 6 below. The polymeric acrylate refers to the polyester and urethane acrylates (i, ii). The tetra-acrylate refers to the tetra-functional acrylate oligomer (iii). The tri-acrylate refers to the tri-functional acrylate oligomers (iv, v). The di-acrylate refers to the di-functional acrylate oligomers (vi, vii). The mono-acrylate refers to the mono-functional acrylates (viii, ix)
Next 3.38 grams of amine synergist and 4.4 grams of photoinitiator were added with high speed agitation until completely dissolved in the mixture. The photoinitiator included 3.52 grams of diphenyl ketone and 0.88 grams of 1-hydroxy-cyclohexyl phenyl ketone. Additional ingredients include 4.56 grams of filler and surfactant—including 4.06 grams of diamond particle having a particle size of about 6 microns. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Example 6 has a Tg of 48.52° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00452 eq/gm.
Comparative Example 1 was prepared by first mixing together the following ingredients
The urethane acrylate was produced by reacting 34.38 of polyester polyol with 87.41 grams of HDI trimer (Desmodur N-3300) to create an isocyanate-terminated polyester prepolymer. The prepolymer is then reacted with 126.28 grams of caprolactone modified hydroxyl acrylate monomer (Tone M-100) having two repeating units of caprolactone to create the acrylate functional terminated polyester based urethane (“urethane acrylate”).
The relative amount of each reactive component can be summarized in Table 7 below. The polymeric acrylate refers to the urethane acrylate (i). The tri-acrylate refers to the tri-functional acrylate oligomers (ii). The polysiloxane refers to compound iii.
Next 3.88 grams of diphenyl ketone photoinitiator were added with high speed agitation until completely dissolved in the mixture. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a flexible vinyl substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Comparative Example 1 has a Tg of 18° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00350 eq/gm.
Comparative Example 2 was prepared by first mixing together the following ingredients
The urethane acrylate was produced according to the methodology set forth in Comparative Example 1. The relative amount of each reactive component can be summarized in Table 8 below. The polymeric acrylate refers to the urethane acrylate (i). The tri-acrylate refers to the tri-functional acrylate oligomers (ii). The polysiloxane refers to compound iii.
Next 6.67 grams of diphenyl ketone photoinitiator and 15 grams of benzophenone photoinitiator were added with high speed agitation until completely dissolved in the mixture. Finally, matting agent was added, which includes the following:
The matting agent was added slowly, the mixture is agitated for at least 10 minutes with high speed agitation. After the high speed agitation, the resulting curable coating composition is discharged from the mixer and applied to a substrate by roll coating. Once applied to the substrate, the curable coating composition is cured by UV radiation, thereby forming the coating layer of the floor covering.
The resulting coating layer of Comparative Example 2 has a Tg of 18° C. and a carbon-carbon double bond linkage per unit of mass (thereby indicating cross-link density of the cured coating layer) of 0.00309 eq/gm.
Each coating layer was when tested for stain resistance by first measuring the initial yellow color value (b*) of the coating layer atop the corresponding substrate. Next, iodine was applied to each coating layer and left for an average of 3 minutes and then wiped away. After wiping away the iodine stain, the color value for each coating layer atop the corresponding substrate was again measured. The resulting change in color value (Δb=final color value−initial color value) was then recorded and compared against each test sample—with a corresponding assignment of pass or fail based on the total amount of color change for each example. The results are provided in Table 9.
As those skilled in the art will appreciate, numerous changes and modifications may be made to the embodiments described herein, without departing from the spirit of the invention. It is intended that all such variations fall within the scope of the invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2016/062133 | 11/16/2016 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62255714 | Nov 2015 | US |
