The present invention relates to a coating composition for metal with improved oil resistance and adhesion and a method for preparing the same, and a metallic article coated with the composition, and more specifically, the present invention relates to a coating composition which comprises (meth)acryl-modified polyurethane comprising polymerized units derived from anhydrosugar alcohol-alkylene oxide adduct, (meth)acrylic monomer, and epoxy resin, and can provide a coating with excellent adhesion to metal and improved oil resistance at the same time, and a method for preparing the same, and a metallic article coated with the composition.
Polyols and isocyanates, which are essential components for polyurethane, are usually prepared from petroleum-based raw materials. However, in the field of polyurethane, due to various reasons such as accelerated depletion of petroleum resources, demand to reduce greenhouse gas emissions according to climate change, rise of raw material prices, and increasing need for recyclable raw materials, a method for partially or completely replacing polyols and isocyanates prepared from petroleum-based raw materials with environmentally friendly components has been requested.
Polyols can be produced from recyclable biomass such as natural vegetable oils, cellulose, lignin, etc., and biopolyols derived from natural vegetable oils are already being produced on a commercial scale. The properties of biopolyol produced become different according to the type of biomass used for the production. In general, castor oil, palm oil, etc. are used for the production of soft and hard polyurethanes and synthetic polyols, and soybean oil is used for the production of polyols for soft polyurethane. However, the currently produced biomass-based biopolyol has a disadvantage in that it has a high viscosity.
Natural vegetable oil-based isocyanates are essentially aliphatic compounds, which have a disadvantage in that they are less reactive than aromatic diisocyanates which are based on petroleum. Therefore, research on preparing diisocyanate using biomass has not been conducted much.
Hydrogenated sugar (also referred to as “sugar alcohol”) means a compound obtained by adding hydrogen to the reductive end group in sugar, and generally has a chemical formula of HOCH2(CHOH)nCH2OH wherein n is an integer of 2 to 5. According to the number of carbon atoms, hydrogenated sugar is classified into tetritol, pentitol, hexitol and heptitol (4, 5, 6 and 7 carbon atoms, respectively). Among them, hexitol having 6 carbon atoms includes sorbitol, mannitol, iditol, galactitol, etc. and in particular, sorbitol and mannitol are very useful materials.
Anhydrosugar alcohol is a material formed by removing one or more molecules of water from inside of the hydrogenated sugar. It has a tetraol form with four hydroxyl groups in the molecule when one molecule of water is removed, and a diol form with two hydroxyl groups in the molecule when two molecules of water are removed, and can be produced by using hexitol derived from starch (for example, Korean Patent No. 10-1079518 and Korean Laid-open Patent Publication No. 10-2012-0066904). Because anhydrosugar alcohol is an environmentally friendly material derived from recyclable natural resources, it has received much interest for a long time and researches on its production continue to proceed. Among such anhydrosugar alcohols, isosorbide produced from sorbitol has the widest industrial applicability at present.
Anhydrosugar alcohol can be used in various fields including treatment of heart and blood vessel diseases, patch adhesive, medicaments such as mouthwash, etc., solvents for compositions in the cosmetics industry, emulsifiers in the food industry, etc. In addition, it can increase the glass transition temperature of polymer materials like polyester, PET, polycarbonate, polyurethane, epoxy resin, etc., and improve the strength of such materials. Furthermore, because anhydrosugar alcohol is an environmentally friendly material derived from natural resources, it is very useful in the plastics industry such as bioplastics and the like. It is also known that anhydrosugar alcohol can be used as an adhesive, environmentally friendly plasticizer, biodegradable polymer, and environmentally friendly solvent for water-soluble lacquer.
As such, anhydrosugar alcohol is receiving much interest because of its wide applicability, and the level of practical industrial application thereof is increasing.
Korean Laid-open Patent Publication No. 10-2017-0125328 discloses preparation of an electroconductive adhesive for metal-metal interface from acryl-modified polyurethane and other acrylic monomers in the presence of thermal polymerization initiator. However, an adhesive composition prepared as such has insufficient oil resistance and adhesion thereof should be further improved.
The purpose of the present invention is to provide a coating composition for metal which utilizes (meth)acryl-modified polyurethane comprising polymerized units derived from anhydrosugar alcohol derivative, and thus can provide a coating with excellent adhesion to metal and improved oil resistance at the same time as well as good eco-friendliness, and a method for preparing the same, and a metallic article coated with the composition.
In order to achieve the above-stated purpose, the present invention provides a coating composition for metal comprising, based on total 100 parts by weight of the composition, 5.1 to 64.9 parts by weight of (meth)acryl-modified polyurethane; 7.1 to 74.9 parts by weight of (meth)acrylic monomer; 2.1 to 44.9 parts by weight of epoxy resin; 0.051 to 2.49 parts by weight of epoxy curing promotor; and 0.00051 to 2.49 parts by weight of thermal polymerization initiator, wherein the (meth)acryl-modified polyurethane comprises i) polymerized units derived from anhydrosugar alcohol-alkylene oxide adduct; ii) polymerized units derived from polyisocyanate; and iii) polymerized units derived from hydroxyalkyl (meth)acrylate.
In other aspect, the present invention provides a method for preparing a coating composition for metal, comprising the step of mixing, based on total 100 parts by weight of the mixture, 5.1 to 64.9 parts by weight of (meth)acryl-modified polyurethane; 7.1 to 74.9 parts by weight of (meth)acrylic monomer; 2.1 to 44.9 parts by weight of epoxy resin; 0.051 to 2.49 parts by weight of epoxy curing promotor; and 0.00051 to 2.49 parts by weight of thermal polymerization initiator, wherein the (meth)acryl-modified polyurethane comprises i) polymerized units derived from anhydrosugar alcohol-alkylene oxide adduct; ii) polymerized units derived from polyisocyanate; and iii) polymerized units derived from hydroxyalkyl (meth)acrylate.
In another aspect, the present invention provides a coated metallic article comprising a metallic article; and a coating layer of the coating composition for metal of the present invention on the surface of the metallic article.
The coating composition for metal according to the present invention has excellent adhesion to metal and excellent oil resistance after the coating at the same time, and high curing rate, and thus it can provide a coating with excellent adhesion and oil resistance on metal surface rapidly, and also has good eco-friendliness since it utilizes anhydrosugar alcohol derived from natural resources.
The present invention is explained in more detail below.
The coating composition for metal of the present invention comprises (meth)acryl-modified polyurethane; (meth)acrylic monomer; epoxy resin; epoxy curing promotor; and thermal polymerization initiator.
The (meth)acryl-modified polyurethane comprised in the present coating composition for metal comprises i) polymerized units derived from anhydrosugar alcohol-alkylene oxide adduct; ii) polymerized units derived from polyisocyanate; and iii) polymerized units derived from hydroxyalkyl (meth)acrylate.
The anhydrosugar alcohol-alkylene oxide adduct (also referred to as “anhydrosugar alcohol-alkylene glycol”) is an adduct obtained by reacting hydroxyl group(s) at both ends or one end (preferably both ends) of anhydrosugar alcohol with alkylene oxide, and it means a compound in a form wherein hydrogen(s) of hydroxyl group(s) at both ends or one end (preferably both ends) of anhydrosugar alcohol is(are) substituted with hydroxyalkyl group(s) which is a ring-opened form of alkylene oxide.
In an embodiment, the alkylene oxide may be a linear alkylene oxide having 2 to 8 carbons or a branched alkylene oxide having 3 to 8 carbons, and more concretely, it may be selected from ethylene oxide, propylene oxide or a combination thereof.
The anhydrosugar alcohol can be prepared by dehydration reaction of hydrogenated sugar derived from natural product. Hydrogenated sugar (also referred to as “sugar alcohol”) means a compound obtained by adding hydrogen to the reductive end group in sugar, and generally has a chemical formula of HOCH2(CHOH)nCH2OH wherein n is an integer of 2 to 5. According to the number of carbon atoms, hydrogenated sugar is classified into tetritol, pentitol, hexitol and heptitol (4, 5, 6 and 7 carbon atoms, respectively). Among them, hexitol having 6 carbon atoms includes sorbitol, mannitol, iditol, galactitol, etc. and in particular, sorbitol and mannitol are very useful materials.
The anhydrosugar alcohol may be monoanhydrosugar alcohol, dianhydrosugar alcohol or a mixture thereof, and although it is not especially limited, dianhydrosugar alcohol can be used.
Monoanhydrosugar alcohol is an anhydrosugar alcohol formed by removing one molecule of water from inside of the hydrogenated sugar, and it has a tetraol form with four hydroxyl groups in the molecule. In the present invention, the kind of the monoanhydrosugar alcohol is not especially limited, and it may be preferably monoanhydrohexitol, and more concretely 1,4-anhydrohexitol, 3,6-anhydrohexitol, 2,5 -anhydrohexitol, 1,5-anhydrohexitol, 2,6-anhydrohexitol or a mixture of two or more of the foregoing.
Dianhydrosugar alcohol is an anhydrosugar alcohol formed by removing two molecules of water from inside of the hydrogenated sugar, and it has a diol form with two hydroxyl groups in the molecule, and can be produced by using hexitol derived from starch. Because dianhydrosugar alcohol is an environmentally friendly material derived from recyclable natural resources, it has received much interest for a long time and researches on its production continue to proceed. Among such dianhydrosugar alcohols, isosorbide produced from sorbitol has the widest industrial applicability at present.
In the present invention, the kind of the dianhydrosugar alcohol is not especially limited, and it may be preferably dianhydrohexitol, and more concretely 1,4:3,6-dianhydrohexitol. 1,4:3,6-dianhydrohexitol may be isosorbide, isomannide, isoidide or a mixture of two or more of the foregoing.
In an embodiment, the anhydrosugar alcohol-alkylene oxide adduct may be a compound represented by the following formula 1, or a mixture of two or more of such compounds.
In the above formula 1,
More preferably, in the above formula 1,
In an embodiment, the anhydrosugar alcohol-alkylene oxide adduct may be anhydrosugar alcohol-propylene oxide adduct represented by the following formula 1-1, anhydrosugar alcohol-ethylene oxide adduct represented by the following formula 1-2, or a mixture thereof.
In the above formula 1-1,
More preferably, in the above formula 1-1,
In the above formula 1-2,
More preferably, in the above formula 1-2,
In an embodiment, the anhydrosugar alcohol-alkylene oxide adduct may be that prepared by a preparation method comprising the steps of: (1) treating anhydrosugar alcohol with acid component; and (2) conducting addition reaction of the acid-treated anhydrosugar alcohol obtained in said step (1) and alkylene oxide.
More concretely, the anhydrosugar alcohol-alkylene oxide adduct may be that prepared by a preparation method comprising the steps of: (1) treating anhydrosugar alcohol with acid component; (2) conducting addition reaction of the acid-treated anhydrosugar alcohol obtained in said step (1) and alkylene oxide; and (3) conducting addition reaction of the product obtained in said step (2) and alkylene oxide in the presence of base catalyst.
The acid component is not especially limited, and it may be selected from the group consisting of phosphoric acid, sulfuric acid, acetic acid, formic acid, heteropolyacid or a mixture thereof. In an embodiment, as the heteropolyacid, phosphotungstic acid, phosphomolybdic acid, silicotungstic acid or silicomolybdic acid, etc. may be used, and as other useful acid component, a commercially available acid component such as Amberlyst 15 (Dow Chemical), etc. can be used, too.
In an embodiment, the acid treatment can be conducted by using the acid component in an amount of 0.1 to 10 moles, preferably 0.1 to 8 moles, and more preferably 0.1 to 5 moles, based on 1 mole of anhydrosugar alcohol, under nitrogen atmosphere at an elevated temperature (for example, 80° C. to 200° C., or 90° C. to 180° C.), and then conducting pressure reduction under vacuum to remove moisture in the reactor, but it is not limited thereto.
The acid component is used in the above acid treatment to facilitate the ring opening of alkylene oxide in the addition reaction of alkylene oxide explained below.
In general, the reaction of adding alkylene oxide to alcohol proceeds under a base catalyst, but in case of anhydrosugar alcohol, due to structural characteristics, the rate of adding the alkylene oxide competes with the rate of opening and decomposition of the ring structure of anhydrosugar alcohol by the base catalyst. Accordingly, not only the anhydrosugar alcohol but also the decomposition product of the anhydrosugar alcohol reacts with the alkylene oxide, and the reaction product between the decomposition product of the anhydrosugar alcohol decomposed by the base catalyst and the alkylene oxide may act as a factor to lower product quality and storage stability. To the contrary, if anhydrosugar alcohol is first treated with an acid component and then subjected to addition reaction of alkylene oxide, the acid component facilitates the ring opening of the alkylene oxide without generating decomposition products of the anhydrosugar alcohol by the base catalyst, and thus anhydrosugar alcohol-alkylene oxide adduct can be easily produced by addition reaction of anhydrosugar alcohol and alkylene oxide. Therefore, when the acid-treated anhydrosugar alcohol and alkylene oxide are subjected to addition reaction, the conventional problems can be solved.
In an embodiment, the addition reaction of the acid-treated anhydrosugar alcohol and alkylene oxide can be conducted by slowly feeding alkylene oxide to the acid-treated anhydrosugar alcohol at an elevated temperature (for example, 100° C. to 180° C., or 120° C. to 160° C.) during a time of, for example, 1 hour to 8 hours, or 2 hours to 4 hours, but it is not limited thereto. The reaction molar ratio of alkylene oxide to 1 mole of anhydrosugar alcohol may be, for example, 1 mole or more, or 2 moles or more, and 30 moles or less, 20 moles or less, 15 moles or less, or 12 moles or less, and for example, it may be 1 mole to 30 moles, preferably 2 to 20 moles, but it is not limited thereto.
In an embodiment, the further addition reaction of the product obtained by addition reaction of alkylene oxide with additional alkylene oxide can be conducted, for example, in high pressure reactor capable of being pressurized (for example, pressurized to 3MPa or higher) in the presence of base catalyst (for example, alkali metal hydroxide such as sodium hydroxide, potassium hydroxide, etc. or alkaline earth metal hydroxide such as calcium hydroxide, etc.) at an elevated temperature (for example, 100° C. to 180° C., or 120° C. to 160° C.) during a time of, for example, 1 hour to 8 hours, or 2 hours to 4 hours, but it is not limited thereto. The reaction molar ratio of the alkylene oxide to 1 mole of anhydrosugar alcohol may be, for example, 1 mole or more, 2 moles or more, or 3 moles or more, and 30 moles or less, 20 moles or less, 15 moles or less, or 12 moles or less, and for example, it may be 1 mole to 30 moles, preferably 2 to 20 moles, more preferably 3 to 15 moles, but it is not limited thereto. Prior to feeding of the base catalyst, the acid component used in the treatment can be filtered and removed.
The product obtained by the addition reaction of the acid-treated anhydrosugar alcohol and alkylene oxide (i.e., a compound in a form where alkylene oxide is added to anhydrosugar alcohol) has a very stable structure, and thus even in the presence of base catalyst, the ring structure of the anhydrosugar alcohol is neither easily opened nor decomposed at high temperature. Therefore, it is very advantageous for further addition reaction of alkylene oxide. If it is continued to use the acid catalyst even during the further additional reaction of alkylene oxide, the acid catalyst helps to promote ring opening of alkylene oxide, but the reaction rate decreases as the number of moles of added alkylene oxide increases. That is, the rate of adding alkylene oxide and the rate of ring opening of the alkylene oxide itself compete, and at this time, the rate of adding alkylene oxide becomes slow, and the self-condensation reaction between the ring-opened alkylene oxides and the generation of byproduct proceed, which may cause deterioration of quality. Therefore, the further addition reaction of alkylene oxide is conducted under base catalyst.
Thereafter, the step of removing metal ions released from the used base catalyst may be conducted additionally, and for this, a metal ion adsorbent such as, for example, Ambosol MP20 (magnesium silicate component) may be used.
In an embodiment, example of the polyisocyanate may be aromatic polyisocyanate such as methylenediphenyl diisocyanate (MDI) (for example, 2,4- or 4,4′-methylenediphenyl diisocyanate), xylylene diisocyanate (XDI), m- or p-tetramethylxylylene diisocyanate (TMXDI) , toluene diisocyanate (TDI), di- or tetra-alkyldiphenylmethane diisocyanate, 3,3′-dimethyldiphenyl-4,4′-diisocyanate (TODI), phenylene diisocyanate (for example, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate), naphthalene diisocyanate (NDI), or 4,4′-dibenzyl diisocyanate, etc.; aliphatic polyisocyanate such as hydrogenated MDI (H12MDI), 1-methyl-2,4-diisocyanatocyclohexane, 1,12-diisocyanatododecane, 1,6-diisocyanato-2,2,4-trimethylhexane, 1,6-diisocyanato-2,4,4-trimethylhexane, isophorone diisocyanate (IPDI), tetramethoxybutane-1,4-diisocyanate, butane-1,4-diisocyanate, hexamethylene diisocyanate (HDI) (for example, 1,6-hexamethylene diisocyanate), dimer fatty acid diisocyanate, dicyclohexylmethane diisocyanate, cyclohexane diisocyanate (for example, cyclohexane-1,4-diisocyanate) or ethylene diisocyanate, etc.; or a combination thereof, but it is not limited thereto.
In other embodiment, example of the polyisocyanate may be methylenediphenyl diisocyanate (MDI), ethylene diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 1,12-dodecane diisocyanate, cyclobutane-1,3-diisocyanate, cyclohexane-1,3-diisocyanate, cyclohexane-1,4-diisocyanate, isophorone diisocyanate, 2,4-hexahydrotoluene diisocyanate, 2,6-hexahydrotoluene diisocyanate, dicyclohexylmethane-4,4′-diisocyanate (HMDI), 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, mixed toluene diisocyanate of 2,4-toluene diisocyanate and 2,6-toluene diisocyanate (2,4-/2,6-isomer ratio=80/20), diphenylmethane-2,4′ -diisocyanate, diphenylmethane-4,4′ -diisocyanate, polydiphenylmethane diisocyanate (PMDI), naphthalene-1,5-diisocyanate, or a combination thereof, but it is not limited thereto.
More concretely, the polyisocyanate may be methylenediphenyl diisocyanate (MDI), toluene diisocyanate (TDI), hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), or a combination thereof.
In an embodiment, example of the hydroxyalkyl (meth)acrylate may be a linear or branched alkyl acrylate having hydroxyl group, a linear or branched alkyl methacrylate having hydroxyl group, or a combination thereof, and more concretely, it may be a linear or branched C1-C8 alkyl acrylate having hydroxyl group, a linear or branched C1-C8 alkyl methacrylate having hydroxyl group, or a combination thereof, and still more concretely, it may be hydroxymethyl acrylate, hydroxymethyl methacrylate, hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate, hydroxypentyl acrylate, hydroxypentyl methacrylate, 2-hydroxyethylhexyl acrylate, 2-hydroxyethylhexyl methacrylate, 2-hydroxyethylbutyl acrylate, 2-hydroxyethylbutyl metacrylate, hydroxyoctyl acrylate, hydroxyoctyl methacrylate, or a combination thereof, and still more concretely, it may be 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate, or a combination thereof, but it is not limited thereto.
In an embodiment, the (meth)acryl-modified polyurethane of the present invention may be represented by the following formula 2:
In the above formula 2,
M is a divalent organic group derived from anhydrosugar alcohol, concretely it is a divalent organic group derived from isosorbide, isomannide or isoidide, and more concretely it is selected from the following formulas:
More concretely, the (meth)acryl-modified polyurethane of the present invention may be represented by any one of the following formulas, but it is not limited thereto:
In the above formulas, each of m, n and m+n is independently the same as defined in the above formula 2.
The (meth)acryl-modified polyurethane can be obtained by reacting polyisocyanate to the anhydrosugar alcohol-alkylene oxide adduct and then reacting hydroxyalkyl (meth)acrylate thereto.
In an embodiment, the (meth)acryl-modified polyurethane can be prepared by a method comprising the steps of: (1) reacting anhydrosugar alcohol-alkylene oxide adduct and polyisocyanate to prepare intermediate having terminal isocyanate group; and (2) reacting the intermediate obtained in said step (1) and hydroxyalkyl (meth)acrylate.
According to an embodiment, the (meth)acryl-modified polyurethane can be prepared by reacting 2 equivalents of diisocyanate to 1 equivalent of anhydrosugar alcohol (e.g., isosorbide (ISB))-alkylene oxide adduct to prepare intermediate having terminal isocyanate group, and then reacting the terminal isocyanate group of the intermediate with 2 equivalents of hydroxyalkyl (meth)acrylate (e.g., 2-hydroxyethyl methacrylate).
In case of acryl-modified polyurethane prepared by using a general alkylene oxide (for example, ethylene oxide or polypropylene oxide, etc.) rather than the anhydrosugar alcohol-alkylene oxide adduct, the oil resistance of the coating formed from a composition comprising it is lowered (when polypropylene oxide is applied), or the adhesion of the coating formed from a composition comprising it is lowered (when ethylene oxide is applied).
According to an embodiment, the reaction of the anhydrosugar alcohol-alkylene oxide adduct and polyisocyanate may be conducted optionally in the presence of catalyst (for example, tin-based catalyst such as dibutyltin dilaurate (DBTDL)) at room temperature or an elevated temperature (for example, at 50 to 100° C., preferably at 50 to 70° C.) during a proper time (for example, 0.1 to 5 hours, preferably 0.5 to 2 hours).
According to an embodiment, the reaction of the product of reacting anhydrosugar alcohol-alkylene oxide adduct and polyisocyanate (i.e., the intermediate obtained in the above step (1)) and hydroxyalkyl (meth)acrylate may be conducted optionally in the presence of catalyst (for example, tin-based catalyst such as dibutyltin dilaurate (DBTDL)) at an elevated temperature (for example, at 50 to 100° C., preferably at 50 to 70° C.) during a proper time (for example, 0.1 to 5 hours, preferably 0.5 to 2 hours).
The coating composition for metal of the present invention comprises, based on total 100 parts by weight of the composition, 5.1 to 64.9 parts by weight of the (meth)acryl-modified polyurethane. If the amount of the (meth)acryl-modified polyurethane in 100 parts by weight of the composition is less than 5.1 parts by weight, the adhesion of the coating formed from a composition comprising it becomes poor and the oil resistance thereof becomes very poor, and to the contrary, if the amount is greater than 64.9 parts by weight, the adhesion of the coating formed from a composition comprising it becomes poor.
More concretely, the amount of the (meth)acryl-modified polyurethane in 100 parts by weight of the coating composition for metal of the present invention may be, for example, 5.1 parts by weight or more, 5.5 parts by weight or more, 6 parts by weight or more, 6.5 parts by weight or more, 7 parts by weight or more, 7.5 parts by weight or more, 8 parts by weight or more, 8.5 parts by weight or more, 9 parts by weight or more, 9.5 parts by weight or more, or 10 parts by weight or more, and it also may be 64.9 parts by weight or less, 64.5 parts by weight or less, 64 parts by weight or less, 63.5 parts by weight or less, 63 parts by weight or less, 62.5 parts by weight or less, 62 parts by weight or less, 61.5 parts by weight or less, 61 parts by weight or less, 60.5 parts by weight or less, or 60 parts by weight or less, but it is not limited thereto.
The (meth)acrylic monomer comprised in the present coating composition for metal is capable of adjusting the viscosity of the coating composition for metal so as to improve its workability such as applicability on metal, etc., increasing the thermal curing rate of the coating composition for metal, and enhancing the strength of the cured product so as to improve its adhesion.
The (meth)acrylic monomer contained in the present coating composition for metal may be a monomer having (meth)acrylic group in the molecule, and preferably, it may be a monomer having 1 to 6 (concretely, 1 to 4) (meth)acrylic groups in the molecule, or a mixture of two or more thereof.
In an embodiment, as the (meth)acrylic monomer, a monomer having 1 (meth)acrylic group may be, for example, (meth)acrylic acid, lauryl (meth)acrylate, stearyl (meth)acrylate, ethylcarbitol (meth)acrylate, tetrahydrofurfuryl (meth)acrylate, caprolactone-modified tetrahydrofurfuryl (meth)acrylate, cyclohexyl (meth)acrylate, dicyclopentanyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, phenyl (meth)acrylate, phenoxyethyl (meth)acrylate , phenoxydiethyleneglycol (meth) acrylate, phenoxytetraethyleneglycol (meth)acrylate, nonylphenoxyethyl (meth)acrylate, nonylphenoxytetraethyleneglycol (meth)acrylate, methoxydiethyleneglycol (meth)acrylate, ethoxydiethyleneglycol (meth)acrylate, butoxyethyl (meth)acrylate, butoxytriethyleneglycol (meth)acrylate, 2-ethylhexylpolyethyleneglycol (meth)acrylate, nonylphenylpolypropyleneglycol (meth)acrylate, methoxydipropyleneglycol (meth)acrylate, glycidyl (meth)acrylate, 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, glycerol (meth)acrylate, polyethyleneglycol (meth)acrylate, polypropyleneglycol (meth)acrylate, epichlorohydrin (hereinafter abbreviated as ECH)-modified butyl (meth)acrylate, ECH-modified phenoxy (meth)acrylate, ethylene oxide (hereinafter abbreviated as EO)-modified phthalic acid (meth)acrylate, EO-modified succinic acid (meth)acrylate, caprolactone-modified 2-hydroxyethyl (meth)acrylate, N,N-dimethylaminoethyl (meth)acrylate, N,N-diethylaminoethyl (meth)acrylate, (2-methyl-2-ethyl-1,3-dioxolan-4-yl)methyl (meth)acrylate, or a mixture thereof, but it is not limited thereto.
In other embodiment, as the (meth)acrylic monomer, a monomer having 2 or more (meth)acrylic groups may be, for example, 1,6-hexanediol diacrylate (HDDA), 1,4-butanediol diacrylate (BDDA), tripropyleneglycol diacrylate (TPGDA), bisphenol A [EO]4˜30 diacrylate (BPA[EO]4˜30DA, EO is ethylene oxide unit), trimethylolpropane triacrylate (TMPTA), trimethylolpropane [EO]3˜15 triacrylate (TMP[EO]3˜5TH, EO is ethylene oxide unit), pentaerythritol triacrylate (PETA), pentaerythritol tetraacrylate (PETTA), ditrimethylolpropane tetraacrylate (DTMPTTA), dipentaerylthritol pentaacrylate (DPPA), dipentaerythritol hexaacrylate (DPHA), or a mixture thereof, but it is not limited thereto.
The coating composition for metal of the present invention comprises, based on total 100 parts by weight of the composition, 7.1 to 74.9 parts by weight of the (meth)acrylic monomer. If the amount of the (meth)acrylic monomer in 100 parts by weight of the composition is less than 7.1 parts by weight, the adhesion of the coating formed from a composition comprising it becomes very poor and the oil resistance thereof becomes poor, and to the contrary, if the amount is greater than 74.9 parts by weight, the oil resistance of the coating formed from a composition comprising it becomes very poor.
More concretely, the amount of the (meth)acrylic monomer in 100 parts by weight of the coating composition for metal of the present invention may be, for example, 7.1 parts by weight or more, 7.5 parts by weight or more, 8 parts by weight or more, 8.5 parts by weight or more, 9 parts by weight or more, 9.5 parts by weight or more, or 10 parts by weight or more, and it also may be 74.9 parts by weight or less, 74.5 parts by weight or less, 74 parts by weight or less, 73.5 parts by weight or less, 73 parts by weight or less, 72.5 parts by weight or less, 72 parts by weight or less, 71.5 parts by weight or less, 71 parts by weight or less, 70.5 parts by weight or less, or 70 parts by weight or less, but it is not limited thereto.
The epoxy resin comprised in the present coating composition for metal is used to enhance the strength of the cured product of the coating composition for metal and so improve its adhesion.
The epoxy resin is a resin having epoxy group in the molecule, and preferably, it may be a resin having 2 or more epoxy groups in the molecule, or a mixture of two or more thereof
In an embodiment, the epoxy resin may be, for example, bisphenol-based epoxy resin, phenol novolac-based epoxy resin, o-cresol novolac-based epoxy resin, multifunctional epoxy resin, amine-based epoxy resin, heterocycle-containing epoxy resin, substituted epoxy resin, naphthol-based epoxy resin, or a mixture thereof, but it is not limited thereto.
The coating composition for metal of the present invention comprises, based on total 100 parts by weight of the composition, 2.1 to 44.9 parts by weight of the epoxy resin. If the amount of the epoxy resin in 100 parts by weight of the composition is less than 2.1 parts by weight, the adhesion of the coating formed from a composition comprising it becomes poor, and to the contrary, if the amount is greater than 44.9 parts by weight, the adhesion and oil resistance of the coating formed from a composition comprising it become poor.
More concretely, the amount of the epoxy resin in 100 parts by weight of the coating composition for metal of the present invention may be, for example, 2.1 parts by weight or more, 2.5 parts by weight or more, 3 parts by weight or more, 3.5 parts by weight or more, 4 parts by weight or more, 4.5 parts by weight or more, or 5 parts by weight or more, and it also may be 44.9 parts by weight or less, 44.5 parts by weight or less, 44 parts by weight or less, 43.5 parts by weight or less, 43 parts by weight or less, 42.5 parts by weight or less, 42 parts by weight or less, 41.5 parts by weight or less, 41 parts by weight or less, 40.5 parts by weight or less, 40 parts by weight or less, or 39 parts by weight or less, but it is not limited thereto.
The epoxy curing promotor comprised in the present coating composition for metal is used to increase the curing rate of the epoxy resin.
In an embodiment, the epoxy curing promotor may be, for example, substituted imidazole (e.g., 1-methylimidazole, 2-methylimidazole, 2-ethyl-4-methylimidazole, 2-phenylimidazole, 1-cyanoethylimidazole), imidazoline (e.g., 2-phenylimidazoline), tertiary amine (e.g., N,N-dimethylbenzylamine), 2,4,6-tris(dimethylaminomethyl)phenol (DNIP30), bisphenol A, bisphenol F, nonylphenol, p-tert-butylphenol, novolac type phenolic resin, salicylic acid, p-toluenesulfonic acid, 1,4-diazabicyclo[2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), S-triazine (e.g., Lupragen N600), bis(2-dimethylaminoethyl) ether (e.g., Lupragen N206), pentamethyldiethylenetriamine (e.g., Lupragen N301), trimethylaminoethylethanolamine (e.g., Lupragen N400), tetramethyl-1,6-hexanediamine (e.g., Lupragen N500), aminoethylmorpholine, aminopropylmorpholine, aminoethylethyleneurea, ketimine (e.g., Epi-Kure 3502) (reaction product of ethylene diamine and methyl isobutyl ketone), uron (e.g., 3-(4-chlorophenyl)-1,1-dimethylurea (monuron), 3-(3,4-dichlorophenyl)-1,1-dimethylurea (diuron), 3-phenyl-1,1-dimethylurea (phenuron) and 3-(3-chloro-4-methylphenyl)-1,1-dimethylurea (chlorotolurone)), tolyl-2,4-bis-N,N-dimethylcarbamide (e.g., Amicure UR2T), dicyandiamide (DICY), Mannich base or secondary amine (e.g., dialkylamine such as di(2-ethylhexyl)amine, dibutylamine, dipropylamine, ditridecylamine), N,N′-diisopropylisophoronediamine (e.g., Jefflink® XTJ-584), N,N′-di isobutyl-4,4′-diaminodicyclohexylmethane (e.g., Clearlink 1000), N-(hydroxyethyl)aniline, and di(2-methoxyethyl)amine, or a combination thereof; but it is not limited thereto.
The coating composition for metal of the present invention comprises, based on total 100 parts by weight of the composition, 0.051 to 2.49 parts by weight of the epoxy curing promotor. If the amount of the epoxy curing promotor in 100 parts by weight of the composition is less than 0.051 part by weight, a composition comprising it is not cured and so a coating is not formed therefrom, and to the contrary, if the amount is greater than 2.49 parts by weight, the adhesion and oil resistance of the coating formed from a composition comprising it become very poor.
More concretely, the amount of the epoxy curing promotor in 100 parts by weight of the coating composition for metal of the present invention may be, for example, 0.051 part by weight or more, 0.055 part by weight or more, 0.06 part by weight or more, 0.065 part by weight or more, 0.07 part by weight or more, 0.075 part by weight or more, 0.08 part by weight or more, 0.085 part by weight or more, 0.09 part by weight or more, 0.095 part by weight or more, or 0.1 part by weight or more, and it also may be 2.49 parts by weight or less, 2.45 parts by weight or less, 2.4 parts by weight or less, 2.35 parts by weight or less, 2.3 parts by weight or less, 2.25 parts by weight or less, 2.2 parts by weight or less, 2.15 parts by weight or less, 2.1 parts by weight or less, 2.05 parts by weight or less, 2 parts by weight or less, 1.5 parts by weight or less, or 1 part by weight or less, but it is not limited thereto.
The thermal polymerization initiator comprised in the present coating composition for metal is used to initiate the polymerization of the (meth)acrylic monomer and the (meth)acryl-modified polyurethane and thus promote the curing.
In an embodiment, the thermal polymerization initiator may be selected from compounds represented by the following formula 3-1, compounds represented by the following formula 3-2, or mixtures thereof:
The coating composition for metal of the present invention comprises, based on total 100 parts by weight of the composition, 0.00051 to 2.49 parts by weight of the thermal polymerization initiator. If the amount of the thermal polymerization initiator in 100 parts by weight of the composition is less than 0.00051 part by weight, a composition comprising it is not cured and so a coating is not formed therefrom, and to the contrary, if the amount is greater than 2.49 parts by weight, the adhesion and oil resistance of the coating formed from a composition comprising it become very poor.
More concretely, the amount of the thermal polymerization initiator in 100 parts by weight of the coating composition for metal of the present invention may be, for example, 0.00051 part by weight or more, 0.00055 part by weight or more, 0.0006 part by weight or more, 0.00065 part by weight or more, 0.0007 part by weight or more, 0.00075 part by weight or more, 0.0008 part by weight or more, 0.00085 part by weight or more, 0.0009 part by weight or more, 0.00095 part by weight or more, 0.001 part by weight or more, 0.005 part by weight or more, or 0.01 part by weight or more, and it also may be 2.49 parts by weight or less, 2.45 parts by weight or less, 2.4 parts by weight or less, 2.35 parts by weight or less, 2.3 parts by weight or less, 2.25 parts by weight or less, 2.2 parts by weight or less, 2.15 parts by weight or less, 2.1 parts by weight or less, 2.05 parts by weight or less, 2 parts by weight or less, 1.5 parts by weight or less, 1 part by weight or less, or 0.5 part by weight or less, but it is not limited thereto.
In addition to the components explained above, the coating composition for metal of the present invention can further comprise additive(s) that can be used conventionally in paint compositions for metal.
In other aspect, the present invention provides a method for preparing a coating composition for metal, comprising the step of mixing, based on total 100 parts by weight of the mixture, 5.1 to 64.9 parts by weight of (meth)acryl-modified polyurethane; 7.1 to 74.9 parts by weight of (meth)acrylic monomer; 2.1 to 44.9 parts by weight of epoxy resin; 0.051 to 2.49 parts by weight of epoxy curing promotor; and 0.00051 to 2.49 parts by weight of thermal polymerization initiator, wherein the (meth)acryl-modified polyurethane comprises i) polymerized units derived from anhydrosugar alcohol-alkylene oxide adduct; ii) polymerized units derived from polyisocyanate; and iii) polymerized units derived from hydroxyalkyl (meth)acrylate.
In the method for preparing a coating composition for metal of the present invention, the concrete kinds and use amounts of the (meth)acryl-modified polyurethane, (meth)acrylic monomer, epoxy resin, epoxy curing promotor and thermal polymerization initiator are the same as explained above.
In a preferable embodiment, the mixing of the (meth)acryl-modified polyurethane, (meth)acrylic monomer, epoxy resin, epoxy curing promotor and thermal polymerization initiator can be conducted under temperature condition of 60° C. or lower (e.g., 10 to 60° C., and more concretely, 20 to 60° C.). If the temperature condition for mixing of the components is too higher than 60° C., polymerization reaction of the (meth)acrylic monomer may proceed during the mixing and curing may occur during preparation of the composition, and thus it may be difficult to use the resulting product as a coating composition.
In another aspect, the present invention provides a coated metallic article comprising a metallic article; and a coating layer of the coating composition for metal of the present invention on the surface of the metallic article.
In an embodiment, the metallic article may be a mechanical part, electric part or electronic part, but it is not limited thereto.
There is no special limitation to the method for forming a coating layer of the coating composition for metal of the present invention on the metallic article, and it can be conducted by using a conventional coating method and device.
The present invention is explained in more detail through the following Examples and Comparative Examples. However, the scope of the present invention is not limited thereby in any manner.
146 g of isosorbide and 0.15 g of phosphoric acid (85%) as an acid component were put into a reactor that could be pressurized, and the inside of the reactor was substituted with nitrogen and heated up to 100° C. and the moisture in the reactor was removed by pressure reduction under vacuum. Then, while firstly adding 88 g of ethylene oxide slowly thereto, the reaction was conducted at 100 to 140° C. for 2 to 3 hours. At that time, the reaction temperature was controlled so as not to exceed 140° C. Thereafter, the inside of the reactor was cooled to 50° C., and then 0.3 g of potassium hydroxide was added to the reactor, the inside of the reactor was substituted with nitrogen and heated up to 100° C. and the moisture in the reactor was removed by pressure reduction under vacuum. Then, while secondly adding 132 g of ethylene oxide slowly thereto, the reaction was conducted at 100 to 140° C. for 2 to 3 hours. After completing the reaction, the inside of the reactor was cooled to 50° C., 4.0 g of Ambosol MP20 as adsorbent was added thereto, and the inside of the reactor was reheated and agitated at 100° C. to 120° C. for 1 to 5 hours to remove residual metal ions (at that time, the inside of the reactor was substituted with nitrogen and/or pressure reduction under vacuum was carried out). After confirming that no metal ions were detected, the inside of the reactor was cooled to 60° C. to 90° C. and the remaining byproduct was removed to obtain 362 g of isosorbide-ethylene oxide 5 mole adduct in transparent liquid form.
Excepting that the secondly added amount of ethylene oxide was changed from 132 g to 352 g, the same method as Preparation Example A1 was conducted to obtain 551 g of isosorbide-ethylene oxide 10 mole adduct in transparent liquid form.
As the raw material for the addition reaction, propylene oxide was used instead of ethylene oxide. Concretely, excepting that 116 g of propylene oxide was firstly added instead of 88 g of ethylene oxide and 174 g of propylene oxide was secondly added instead of 132 g of ethylene oxide, the same method as Preparation Example A1 was conducted to obtain 423 g of isosorbide-propylene oxide 5 mole adduct in transparent liquid form.
As the raw material for the addition reaction, propylene oxide was used instead of ethylene oxide. Concretely, excepting that 116 g of propylene oxide was firstly added instead of 88 g of ethylene oxide and 465 g of propylene oxide was secondly added instead of 132 g of ethylene oxide, the same method as Preparation Example A1 was conducted to obtain 698 g of isosorbide-propylene oxide 10 mole adduct in transparent liquid form.
Into a 3-necked glass reactor equipped with an agitator, 222 g of isophorone diisocyanate (IPDI) and 0.1 g of dibutyltin dilaurate (DBTDL) as reaction catalyst were fed. While agitating the mixture at room temperature, 183 g of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 was added slowly thereto and the crosslinking reaction was conducted. After completing addition of the isosorbide-ethylene oxide 5 mole adduct, the mixture was agitated at 50° C. for 1 hour for aging, and 65 g of 2-hydroxyethyl methacrylate was added slowly thereto and the acryl modification reaction was conducted. After completing addition of 2-hydroxyethyl methacrylate, the mixture was agitated at 50° C. for 1 hour for aging, and the reaction product was cooled to room temperature to obtain 467 g of (meth)acryl-modified polyurethane of the following formula A.
Excepting that 168 g of hexamethylene diisocyanate (HDI) was used instead of isophorone diisocyanate (IPDI) as polyisocyanate, 293 g of the isosorbide-ethylene oxide 10 mole adduct prepared in Preparation Example A2 was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol and 58 g of 2-hydroxyethyl acrylate was used instead of 2-hydroxyethyl methacrylate as hydroxyalkyl (meth)acrylate, the same method as Preparation Example B1 was conducted to obtain 515 g of (meth)acryl-modified polyurethane of the following formula B.
Excepting that 250 g of methylenediphenyl diisocyanate (MDI) was used instead of isophorone diisocyanate (IPDI) as polyisocyanate and 218 g of the isosorbide-propylene oxide 5 mole adduct prepared in Preparation Example A3 was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol, the same method as Preparation Example B1 was conducted to obtain 529 g of (meth)acryl-modified polyurethane of the following formula C.
Excepting that 363 g of the isosorbide-propylene oxide 10 mole adduct prepared in Preparation Example A4 was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol, the same method as Preparation Example B1 was conducted to obtain 643 g of (meth)acryl-modified polyurethane of the following formula D.
Excepting that 146 g of isosorbide was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol, the same method as Preparation Example B1 was conducted to obtain 431 g of (meth)acryl-modified polyurethane of the following formula E.
Excepting that 500 g of polyethylene glycol (number average molecular weight: 500 g/mol) was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol, the same method as Preparation Example B1 was conducted to obtain 782 g of (meth)acryl-modified polyurethane of the following formula F.
Excepting that 168 g of hexamethylene diisocyanate (HDI) was used instead of isophorone diisocyanate (IPDI) as polyisocyanate, 500 g of polypropylene glycol (number average molecular weight: 500 g/mol, Kumho Petrochemical) was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol and 58 g of 2-hydroxyethyl acrylate was used instead of 2-hydroxyethyl methacrylate as hydroxyalkyl (meth)acrylate, the same method as Preparation Example B1 was conducted to obtain 720 g of (meth)acryl-modified polyurethane of the following formula G.
Excepting that 250 g of methylenediphenyl diisocyanate (MDI) was used instead of isophorone diisocyanate (IPDI) as polyisocyanate and 1,000 g of polytetramethylene glycol (number average molecular weight: 1,000 g/mol, Aldrich) was used instead of the isosorbide-ethylene oxide 5 mole adduct prepared in Preparation Example A1 as polyol, the same method as Preparation Example B1 was conducted to obtain 1,308 g of (meth)acryl-modified polyurethane of the following formula H.
In a mixing reactor maintained at 60° C. or lower, the (meth)acryl-modified polyurethane, (meth)acrylic monomer, epoxy resin, epoxy curing promotor and thermal polymerization initiator were fed with the weight ratio shown in the following Table 1, and were mixed by agitation at a temperature of 60° C. or lower to prepare a liquid coating composition with oil resistance for metal. At that time, the sum of the amounts of the (meth)acryl-modified polyurethane, (meth)acrylic monomer, epoxy resin, epoxy curing promotor and thermal polymerization initiator was 100 parts by weight in total.
The coating composition with oil resistance for metal prepared in each of Examples A1 to A4 and Comparative Examples A1 to A14 was applied with an area of 2.5 cm×2.0 cm on each surface of two rolled steel sheets cut into 2.5 cm×12 cm size, and then the applied parts of the two rolled steel sheets were overlapped and fixed, and cured by heat at 150° C. for 5 minutes to prepare a metal adhesion sample. For each of the samples, the adhesion and oil resistance were evaluated according to the following methods, and the results are shown in the following Table 2.
In order to evaluate the adhesion to metal of the metal coating composition, the lap shear strength (MPa) of the metal adhesion sample was measured by using UTM (Instron 5967, Instron). Concretely, for each metal adhesion sample, the shear strength was measured 5 times in total, and the average value thereof was calculated. Higher shear strength means better adhesion.
The metal adhesion sample was immersed in mineral oil (Daejung Chemical) and heated at 190° C. for 200 hours, and then for each metal adhesion sample, the shear strength was measured 5 times according to the adhesion measurement method explained in the above (1), and the average value thereof was calculated. Thereafter, for each metal adhesion sample, the reduction ratio (%) of shear strength after immersion to shear strength before immersion was calculated. Lower reduction ratio of shear strength means better oil resistance.
Shear strength reduction ratio (%)=(Shear strength before immersion−Shear strength after immersion)×100/Shear strength before immersion
As shown in Table 2 above, in case of the metal adhesion samples of Examples A1 to A4 for which the coating compositions comprising the (meth)acryl-modified polyurethane according to the present invention were applied, the adhesion to metal was excellent so as to show a shear strength of 16 MPa or higher, and the adhesion was maintained well so as to show a shear strength reduction ratio of less than 30% even after immersion in mineral oil at 190° C. for 200 hours, and thus the oil resistance was also excellent.
However, in case of the metal adhesion samples of Comparative Examples A1 and A2, the adhesion was poor. Also, in case of the metal adhesion samples of Comparative Examples A3 and A4, the shear strength was lowered remarkably after immersion in mineral oil at the high temperature, and thus the oil resistance was poor. In case of the metal adhesion sample of Comparative Example A5, both of the adhesion and oil resistance were very poor, and in case of the metal adhesion sample of Comparative Example A6, the adhesion was poor. In case of the metal adhesion sample of Comparative Example A7, the adhesion was very poor. In case of the metal adhesion sample of Comparative Example A8, the oil resistance was very poor so that spontaneous peeling off of the metal adhesion sample was observed after finishing immersion in mineral oil and heating. In case of the metal adhesion samples of Comparative Examples A9 and A10, the adhesion was poor. In case of the metal adhesion samples of Comparative Examples A11 and A13, the metal coating compositions were not cured, and thus it was impossible to evaluate the adhesion and oil resistance. In case of the metal adhesion samples of Comparative Examples A12 and A14, both of the adhesion and oil resistance were poor.
As explained above, in case of the coating composition for metal comprising the (meth)acryl-modified polyurethane according to the present invention with an amount in a specific range, the adhesion to metal was excellent, and the adhesion was maintained well even in mineral oil at high temperature, and thus the oil resistance was also excellent.
Number | Date | Country | Kind |
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10-2021-0020898 | Feb 2021 | KR | national |
Filing Document | Filing Date | Country | Kind |
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PCT/KR2022/002269 | 2/16/2022 | WO |