Water-based coating composition

专利摘要:
The present invention provides a carboxyl group-containing polyester resin (a) having a number average molecular weight of 1,000 to 30,000 and an acid value of 5 to 200 mgKOH / g, and a 1,2-epoxy group-containing low molecular weight epoxy compound (b) having a number average molecular weight of 1,200 or less, The epoxy-modified polyester resin (A) obtained by the esterification reaction and the carboxyl group-containing acrylic modified polyester resin (B) obtained by reacting the carboxyl group-containing acrylic resin (c) are neutralized and dispersed in an aqueous medium. It is to provide an aqueous coating composition.
公开号:KR20020065913A
申请号:KR1020027008278
申请日:2000-12-21
公开日:2002-08-14
发明作者:히로세유지；나카이노보루；니시다레이지로；누마노부시게
申请人:간사이 페인트 가부시키가이샤；
IPC主号:

专利说明:

Aqueous coating composition {WATER-BASED COATING COMPOSITION}
[2] In order to solve the problem of global environmental pollution by volatilization of organic solvents, the field of can inner coatings such as edible cans is also changing from organic solvent-based paints to water-based paints. In Japanese Unexamined Patent Publication No. 41934 and Japanese Unexamined Patent Application Publication No. 7-138523, an epoxy-based acrylic resin-based aqueous coating obtained by reacting or mixing an epoxy resin with a carboxyl group-containing acrylic resin is proposed.
[3] However, in these conventional aqueous coatings, in terms of obtaining good coating workability and coating film performance as the epoxy resin of the raw material, generally, a high molecular weight epoxy resin obtainable by reacting bisphenol A with a low molecular weight epoxy resin is obtained. Since unreacted bisphenol A remains in the paint, it causes a problem of environmental hormone caused by the remaining bisphenol A. In order to avoid this problem, when using the low molecular weight epoxy resin in which bisphenols are not detected as an epoxy resin of a raw material, the obtained aqueous coating material is a coating film of coating workability, a known adhesiveness, a flavor property, etc. The performance is lowered and is not suitable as a coating material for the inner surface of the can.
[4] Therefore, at present, there is no fundamental solution to the environmental hormone problem caused by bisphenols in water-based paints of epoxy-modified acrylic resins.
[1] The present invention relates to aqueous coating compositions, in particular new aqueous coating compositions suitable for coating can inner surfaces corresponding to environmental hormone problems.
[5] An object of the present invention is to provide a new aqueous coating composition which solves the problems of the prior art.
[6] Another object of the present invention is to provide a novel aqueous coating composition which is excellent in coating workability and coating film performance and can solve the problem of environmental hormone caused by bisphenols.
[7] Still other objects and features of the present invention will become apparent from the following description.
[8] The present invention provides a carboxyl group-containing polyester resin (a) having a number average molecular weight of 1,000 to 30,000 and an acid value of 5 to 200 mgKOH / g and a 1,2-epoxy group-containing low molecular weight epoxy compound (b) having a number average molecular weight of 1,200 or less. Epoxy-modified polyester resin (A) obtained by esterification reaction and carboxyl group-containing acrylic modified polyester resin (B) obtained by reacting carboxyl group-containing acrylic resin (c) are neutralized and dispersed in an aqueous medium. It is to provide an aqueous coating composition.
[9] MEANS TO SOLVE THE PROBLEM This inventor earnestly researched in order to develop the aqueous coating composition suitable for the inner surface of a can which can solve the problem of the environmental hormone by bisphenols. As a result, according to the aqueous coating material which neutralized and disperse | distributed the resin obtained by using these specific carboxyl group-containing polyester resin, the specific low molecular weight epoxy compound in which bisphenols are not detected, and the carboxyl group-containing acrylic resin, and reacting them sequentially, It was found that it did not contain free bisphenols and exhibited the same coating workability and coating film performance as in the case of a conventional epoxy-modified acrylic resin-based aqueous coating. The present invention has been completed based on this new viewpoint.
[10] The epoxy modified polyester resin (A) in the aqueous coating composition of the present invention has a number average molecular weight of 1,000 to 30,000 and a carboxyl group-containing polyester resin (a) having an acid value of 5 to 200 mgKOH / g and a number average molecular weight of 1,200 or less. It is obtained by esterifying the 1,2-epoxy group-containing low molecular weight epoxy compound (b).
[11] The number average molecular weights of the carboxyl group-containing polyester resin (a) are 1,000-30,000, and it is necessary that the acid value is 5-200 mgKOH / g. When the number average molecular weight is less than 1,000 or when the acid value exceeds 200 mgKOH / g, side reactions are liable to occur during the addition reaction of the carboxyl group and the epoxy group, and the viscosity increases, making the production difficult, while the number average molecular weight exceeds 30,000. In the case where the acid value is less than 5 mgKOH / g, water dispersion in the subsequent step becomes difficult, and neither is preferable.
[12] The number average molecular weight of the carboxyl group-containing polyester resin (a) is preferably 2,000 to 10,000, and the acid value is preferably 20 to 150 mgKOH / g.
[13] The carboxyl group-containing polyester resin (a) is obtained by polycondensation reaction of polyhydric alcohol and polybasic acid. Polyhydric alcohols are polyols such as alkane polyols, oxyalkylene polyols, polyoxyalkylene polyols, and alicyclic polyols, and representative examples thereof include ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4 -Butanediol, 1,3-butanediol, 2-methyl-1,3-propanediol, 1,5-pentanediol, 1,3-pentanediol, 1,6-hexanediol, 1,5-hexanediol, neopentyl Alkanes polyols such as glycol, glycerin, 2-methylglycerine, trimethylolpropane, trimethylol ethane and pentane erythritol; Oxyalkylene polyols such as diethylene glycol and dipropylene glycol; Polyoxyalkylene polyols such as triethylene glycol, tetraethylene glycol, polyethylene glycol, tripropylene glycol and polypropylene glycol; Alicyclic polyols, such as 1, 4- cyclohexane dimethanol, etc. are mentioned. As the polybasic acid, for example, adipic acid, sebacic acid, glutaric acid, phthalic acid, isophthalic acid, terephthalic acid, maleic acid, fumaric acid, succinic acid, pimelic acid, azelaic acid, dodecanedioic acid, and cyclohexanedica Leic acid, tetrahydrophthalic acid, methyltetrahydrophthalic acid, endomethylenetetrahydrophthalic acid, methylendomethylenetetrahydrophthalic acid, hexahydrophthalic acid, naphthalenedicarboxylic acid, trimellitic acid, butanetricarboxylic acid or anhydrides thereof Can be mentioned.
[14] In the polycondensation reaction of polyhydric alcohol and polybasic acid, strong protonic acid, heavy metal oxide, etc. can be used as a polycondensation catalyst. As strong protonic acid, a sulfuric acid, benzene sulfonic acid, paratoluene sulfonic acid, etc. are mentioned, for example. Moreover, as a heavy metal oxide, tetrabutyl titanate, dibutyltin oxide, antimony trioxide, manganese dioxide, etc. are mentioned, for example.
[15] The polyester resin (a) can be produced by condensation reaction of a polyhydric alcohol and a polybasic acid so as to have a carboxyl group in a molecule to be a specific acid value of the present invention. In addition, the said resin (a) may first manufacture a hydroxyl-containing polyester resin, and give a specific acid value by adding an acid anhydride to this hydroxyl group, and may manufacture it. Examples of the acid anhydride include phthalic anhydride, trimellitic anhydride, succinic anhydride, maleic anhydride, hexahydrophthalic anhydride, pyromellitic anhydride, and the like.
[16] The 1,2-epoxy group-containing low molecular weight epoxy compound (b) in the present invention needs to have a number average molecular weight of 1,200 or less. In such a low molecular weight epoxy compound, unreacted bisphenols are not detected, and by using this to modify the carboxyl group-containing polyester resin (a), the finally obtained aqueous coating has excellent coating workability and coating film performance. In addition, since free bisphenols are not contained, the problem of environmental hormones is solved.
[17] As said low molecular weight epoxy compound (b), the thing of epoxy equivalent 140-250 and a number average molecular weight 250-900 are preferable.
[18] Examples of the low molecular weight epoxy compound (b) include bisphenol A type epoxy resins such as bisphenol A diglycidyl ether, bisphenol F type epoxy resins such as bisphenol F diglycidyl ether, and dimer acid diglycidyl. Dimer acid deglycidyl ester, polypropylene glycol diglycidyl ether, hydrogenated bisphenol A diglycidyl ether, epoxycyclohexylmethyl epoxyglohexanecarboxylate, epoxyphenol novolac, triglycidyl isocyanurate Non-bisphenol type epoxy resins, such as these, can be used.
[19] Epoxy-modified polyester resin (A) in the composition of the present invention is a carboxyl group-containing polyester resin (a) and a low molecular weight epoxy compound (b), the carboxyl group of the resin (a): the epoxy group of the compound (b) in a molar ratio It can prepare suitably by esterifying by the compounding ratio which becomes 1: 2-1: 1. The epoxy equivalent of the epoxy modified polyester resin (A) obtained by this is about 2,000-10,000, and a number average molecular weight is about 4,000-100,000. As for the said epoxy modified polyester resin (A), it is suitable from the viewpoint of stability, coating workability, coating film performance, etc. that the epoxy equivalent and number average molecular weight are in the said range, and the obtained aqueous coating material.
[20] The epoxy equivalent of the polyester resin (A) is preferably about 2,500 to 7,000, and the number average molecular weight is preferably about 5,000 to 50,000.
[21] The esterification reaction of the said polyester resin (a) and the said low molecular weight epoxy compound (b) for obtaining the said epoxy modified polyester resin (A), for example, these mixtures are tertiary alkylamines and tetraalkyls. In the presence of a catalyst such as an halide of ammonium and an organic solvent, the reaction temperature can be performed at 120 to 150 ° C under a condition of about 1 to 8 hours, whereby the desired resin (A) can be obtained.
[22] Since the said epoxy-modified polyester resin (A) can be obtained by addition reaction between the carboxyl group of a polyester resin (a) terminal, and the 1,2-epoxy group of an epoxy compound (b) terminal normally, a hydroxyl group exists in a molecular side chain. Is generated. The hydroxyl group of this molecular side chain is advantageous for the improvement of the known adhesiveness and corrosion resistance of the coating film obtained by improving adhesiveness with a metal base material.
[23] In the present invention, the carboxyl group-containing acrylic resin (c) used to react with the modified polyester resin (A) to produce a carboxyl group-containing acrylic modified polyester resin (B) is acrylic acid, methacrylic acid, itaconic acid, It is an acrylic polymer which uses polymerizable unsaturated carboxylic acids, such as a fumaric acid, as an essential monomer component. It is preferable that this polymer exists in the range of acid value 100-500 mgKOH / g from a viewpoint of stability in an aqueous medium, processability of the coating film obtained, corrosion resistance, water resistance, etc.
[24] As other monomer components other than polymerizable unsaturated carboxylic acid used for superposition | polymerization of the said acrylic resin (c), for example, methyl (meth) acrylate, ethyl (meth) acrylate, and propyl (meth) acrylate , n-butyl (meth) acrylate, i-butyl (meth) acrylate, t-butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth Alkyl esters having 1 to 18 carbon atoms of acrylic acid or methacrylic acid such as acrylate and cetyl (meth) acrylate; Benzyl (meth) acrylate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate; Aromatic vinyl monomers such as styrene, α-methylstyrene, and vinyltoluene; Hydroxyalkyl (such as hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, hydroxybutyl (meth) acrylate, hydroxyamyl (meth) acrylate, hydroxyhexyl (meth) acrylate ( Hydroxyl group-containing polymerizability, such as a caprolactone modified alkyl (meth) acrylate which has a hydroxyl group formed by carrying out 1-5 mol ring-opening addition reaction of (epsilon) -caprolactone with respect to 1 mol of methacrylates and the said hydroxyalkyl (meth) acrylate. Unsaturated monomers; Acrylamide, methacrylamide, N-methoxymethyl (meth) acrylamide, N-ethoxymethyl (meth) acrylamide, Nn-propoxymethyl (meth) acrylamide, N-isopropoxymethyl (meth) acryl Acrylamide monomers such as amide, Nn-butoxymethyl (meth) acrylamide, N-sec-butoxymethyl (meth) acrylamide, and N-tert-butoxymethyl (meth) acrylamide; Acrylonitrile, methacrylonitrile, vinyl acetate, ethylene, butadiene, etc. are mentioned.
[25] The said acrylic resin (c) is made into the monomer mixture of the said polymerizable unsaturated carboxylic acid and the said other monomer component at 80-150 degreeC in presence of a radical polymerization initiator or a chain transfer agent, for example in an organic solvent. It can obtain by heating and copolymerizing about-10 hours. As said polymerization initiator, things, such as an organic peroxide type and an azo type, can be used. As an organic peroxide type | system | group polymerization initiator, benzoyl peroxide, t-butyl peroxy-2-ethylhexanoate, di-t-butyl peroxide, t-butyl peroxy benzoate, t-amyl peroxy-, for example 2-ethylhexanoate etc. are mentioned, As an azo polymerization initiator, azobisisobutyronitrile, azobisdimethyl valeronitrile (azobisisobutyrovaleronitrile), etc. are mentioned, for example. Moreover, (alpha) -methylstyrene dimer, mercaptans, etc. are mentioned as said chain transfer agent.
[26] The reaction between the epoxy-modified polyester resin (A) and the carboxyl group-containing acrylic resin (c) is usually made of a tertiary amine such as triethylamine, dimethylethanolamine, or triphenylphosphine in an organic solvent. In the presence of a catalyst such as a quaternary salt compound, it can be carried out by heating at a temperature of about 80 to 120 ° C. for about 0.5 to 8 hours and reacting to thereby obtain a carboxyl group-containing acrylic modified polyester resin (B). Can be. In this reaction, esterification usually occurs mainly, but reactions such as onium chloride also occur.
[27] Although the mixing ratio of the epoxy-modified polyester resin (A) and the carboxyl group-containing acrylic resin (c) in the above reaction may be appropriately selected according to coating workability, coating film performance, and the like, the resin (A) / resin (c) As solid content weight ratio, 60/40-90/10 is preferable normally, and it is more preferable to exist in the range of 70/30-90/10.
[28] It is preferable that the carboxyl group-containing acrylic modified polyester resin (B) obtained by the said reaction exists in the range of acid value 15-200 mgKOH / g from the point of dispersion stability in an aqueous medium, the water resistance of the coating film obtained, etc. Moreover, it is preferable from the point of storage stability that it does not have an epoxy group substantially normally.
[29] Although the said acrylic modified polyester resin (B) is neutralized and disperse | distributed in an aqueous medium, as a neutralizing agent used for neutralization, amines and ammonia are used suitably. Representative examples of the amines include triethylamine, triethanolamine, dimethylethanolamine, diethylethanolamine, morpholine, and the like. Especially, triethylamine and dimethylethanolamine are suitable. Although the grade of neutralization of acrylic modified polyester resin (B) is not specifically limited, It is preferable that it is the range of 0.3-1.0 equivalent neutralization normally with respect to the carboxyl group in resin.
[30] The aqueous medium which the carboxyl group-containing acrylic modified polyester resin (B) disperses may be only water, or may be a mixture of water and an organic solvent. As this organic solvent, any conventionally well-known thing can be used as long as it is an organic solvent which can be mixed with water which does not interfere with stability in the aqueous medium of a carboxyl group-containing acrylic modified polyester resin (B).
[31] As the organic solvent, an alcohol solvent, a cellosolve solvent, a carbitol solvent, and the like are preferable. As a specific example of this organic solvent, Alcohol solvents, such as n-butanol; Cellosolve solvents such as ethylene glycol monobutyl ether, ethylene glycol monoisopropyl ether, ethylene glycol monomethyl ether and propylene glycol monomethyl ether; Carbitol solvents, such as diethylene glycol monoethyl ether, etc. are mentioned. Moreover, as an organic solvent, the inert organic solvent which does not mix with water other than the above can also be used in the range which does not interfere with the stability in the aqueous medium of an acrylic modified polyester resin, As such an organic solvent, for example, toluene And aromatic hydrocarbon solvents such as xylene, ester solvents such as ethyl acetate and butyl acetate, and ketone solvents such as methyl ethyl ketone. It is preferable that the quantity of the organic solvent in the aqueous coating composition of this invention is 50 weight% or less in an aqueous medium from a viewpoint of environmental protection.
[32] Neutralizing and dispersing the carboxyl group-containing acrylic modified polyester resin (B) in an aqueous medium is good according to a conventional method, and for example, gradually adding the polyester resin (B) while stirring in an aqueous medium containing a neutralizing agent. After neutralizing the method and the said polyester resin (B) with a neutralizing agent, the method of adding an aqueous medium to this neutralization, or adding this neutralization in an aqueous medium, etc. under stirring is mentioned.
[33] The composition of this invention may contain the crosslinking agent further in addition to the said neutralized carboxyl group-containing acrylic modified polyester resin (B). As a crosslinking agent, resol type phenol resin, melamine resin, benzoguanamine resin, etc. are mentioned. As a phenol component which comprises the said phenol resin, For example, o-cresol, p-cresol, p-tert- butylphenol, p-ethylphenol, 2, 3- xylenol, 2, 5- xylenol, bifunctional phenols such as p-tert-amylphenol, p-nonylphenol, p-cyclohexyl phenol, carbolic acid, m-cresol, m-ethylphenol, 3,5-xylol, trifunctional phenols such as trifunctional phenols such as m-methoxyphenol, monofunctional phenols such as 2,4-xylenol and 2,6-xylenol, and tetrafunctional phenols such as bisphenol B and bisphenol F. (tetrafunctional phenols) and the like or a combination of two or more. However, it is preferable not to use a bisphenol-type phenol resin by the problem of an environmental hormone. Moreover, you may further contain surfactant, an antifoamer, etc. as needed.
[34] It is preferable that solid content rate of the aqueous coating composition of this invention is about 15 to 40 weight% normally.
[35] The composition of the present invention can be suitably used as paints for inner surfaces of cans such as edible cans. For example, zinc, chromium, tin, aluminum, etc. are plated on the surfaces of metal plates such as aluminum plates and steel plates, and steel plates. The surface of the plated steel sheet and the steel sheet can be applied to various metal materials such as treated steel sheet chemically treated with chromic acid, iron phosphate, zinc phosphate and the like. As a means for apply | coating the said composition to the surface of a metal material, well-known arbitrary methods, such as roll coating, spray coating, brush coating, spray coating, immersion electrodeposition coating, etc. are used, for example. Can be used. In addition, the thickness of the coating film is usually sufficient in the range of 2 to 30 µm, and baking of the coating film is generally preferable at about 150 to about 280 ° C, preferably at about 180 to about 220 ° C for about 20 to 600 seconds. Preferably for about 30 to 300 seconds.
[36] Hereinafter, the present invention will be described in more detail with reference to Production Examples, Examples and Comparative Examples. In each example, parts and percentages are based on weight in principle.
[37] Production Example 1: Preparation of carboxyl group-containing acrylic resin
[38] 1,200 parts of ethylene glycol monobutyl ethers were mix | blended with the reaction container, and it heated and maintained at 100 degreeC. A mixed solution of 400 parts of methacrylic acid, 500 parts of styrene, 100 parts of ethyl acrylate, 35 parts of "perbutyl O" (manufactured by Nippon Oil Holding Co., Ltd., peroxide-based polymerization initiator) and 140 parts of ethylene glycol monobutyl ether was added for 3 hours. While dropping. After completion of the dropwise addition, the mixture was aged at 100 ° C for 2 hours, and then 570 parts of n-butanol was added to obtain a carboxyl group-containing acrylic resin solution having a solid content of 36%. The obtained resin had a number average molecular weight of about 7,000 and a resin acid value of 260 mgKOH / g.
[39] Example 1
[40] To the reaction vessel, 310 parts of ethylene glycol, 380 parts of propylene glycol, 234 parts of adipic acid, 580 parts of isophthalic acid, 664 parts of terephthalic acid, 100 parts of cyclohexanone and 0.5 parts of dibutyl tin oxide were mixed, and stirred for 3 hours to 230 ° C. It heated up and kept for 5 hours. Subsequently, after cooling to 160 degreeC, 25 parts of phthalic anhydrides were added and hold | maintained for 2 hours, and the polyester resin solution was obtained. The obtained resin had an acid value of 50 mgKOH / g and a number average molecular weight of about 4,000.
[41] To 1,000 parts of the polyester resin solution, 240 parts of bisphenol A diglycidyl ether (epoxy equivalent about 190, number average molecular weight about 350, residual bisphenol A not detected), 210 parts of cyclohexanone and tri-n-butylamine 0.5 part was mix | blended and hold | maintained at 130 degreeC for 5 hours under stirring, and the epoxy modified polyester resin solution was obtained. The obtained resin had about 3,000 epoxy equivalents and about 20,000 number average molecular weights.
[42] Next, after adding 870 parts of carboxyl group-containing acrylic resin solution of 36% of solid content and 220 parts of ethylene glycol monobutyl ethers to the said epoxy-modified polyester resin solution, and stirring it uniformly, the temperature was 85 degreeC It lowered to and added 77 parts of dimethylethanolamine, and hold | maintained for 1 hour. Then, 3,600 parts of deionized water was dripped over 1 hour, and the aqueous coating composition of this invention which is a water dispersion of resin acid value 37 mgKOH / g, solid content 25%, viscosity 4,000 mPas, and particle diameter 200nm was obtained.
[43] Example 2
[44] To the reaction vessel, 124 parts of ethylene glycol, 152 parts of propylene glycol, 182 parts of adipic acid, 500 parts of isophthalic acid, 660 parts of terephthalic acid, 100 parts of cyclohexanone and 0.5 parts of dibutyl tin oxide were mixed, and stirred for 3 hours to 230 ° C. It heated up over and hold | maintained for 8 hours, and obtained the polyester resin solution. The obtained resin had an acid value of 40 mgKOH / g and a number average molecular weight of about 5,000.
[45] 1,000 parts of the polyester resin solution, 200 parts of bisphenol A diglycidyl ether (epoxy equivalent about 190, number average molecular weight about 350, residual bisphenol A not detected), 200 parts of cyclohexanone and tri-n-butylamine 0.5 part was mix | blended and hold | maintained at 130 degreeC for 3 hours, stirring, and the epoxy modified polyester resin solution was obtained. The obtained resin had about 3,000 epoxy equivalents and about 20,000 number average molecular weights.
[46] Next, 840 parts of the carboxyl group-containing acrylic resin solution of 36% of the solid content obtained in Production Example 1 and 220 parts of ethylene glycol monobutyl ether were added to the epoxy-modified polyester resin solution and uniformly stirred and mixed, and then the temperature was adjusted to 85 ° C. It lowered and added 75 parts of dimethylethanolamines, and hold | maintained for 1 hour. Next, 3,500 parts of deionized water was dripped over 1 hour, and the aqueous coating composition of this invention which is a water dispersion of resin acid value 37 mgKOH / g, solid content 25%, viscosity 3,000 mPas, and particle diameter 250nm was obtained.
[47] Example 3
[48] To the reaction vessel, 155 parts of ethylene glycol, 190 parts of propylene glycol, 230 parts of adipic acid, 530 parts of isophthalic acid, 750 parts of terephthalic acid, 100 parts of cyclohexanone and 0.5 parts of dibutyl tin oxide were mixed, and stirred for 3 hours to 230 ° C. The temperature was raised over and maintained for 8 hours. Subsequently, after cooling to 160 degreeC, 8 parts of phthalic anhydrides were added and hold | maintained for 2 hours, and the polyester resin solution was obtained. The obtained resin had an acid value of 20 mgKOH / g and a number average molecular weight of about 6,000.
[49] To 1,000 parts of the polyester resin solution, 120 parts of bisphenol A diglycidyl ether (epoxy equivalent about 190, number average molecular weight about 350, residual bisphenol A not detected), 200 parts of cyclohexanone, tri-n-butylamine 0.5 part was mix | blended and hold | maintained at 130 degreeC for 3 hours under stirring, and the epoxy modified polyester resin solution was obtained. The obtained resin had about 3,000 epoxy equivalents and about 20,000 number average molecular weights.
[50] Next, after adding 780 parts of carboxyl group-containing acrylic resin solution of 36% of solid content obtained in the manufacture example 1, and 220 parts of ethylene glycol monobutyl ether to the said epoxy-modified polyester resin solution, and stirring it uniformly, the temperature was 85 degreeC 70 parts of dimethylethanolamines were added, and it hold | maintained for 1 hour. Then, 3,200 parts of deionized water was dripped over 1 hour, and the aqueous coating composition of this invention which is a water dispersion of resin acid value 37 mgKOH / g, solid content 25%, viscosity 3,000 mPas, and particle diameter 300nm was obtained.
[51] Comparative Example 1
[52] In the reaction vessel, 1,000 parts of bisphenol A diglycidyl ether (about epoxy equivalent about 190, number average molecular weight about 350, residual bisphenol A not detected), 556 parts of bisphenol A, 172 parts of ethylene glycol monobutyl ether and 50% tetramethyl 1.6 parts of aqueous ammonium solutions were added, it heated up at 140 degreeC under stirring, and hold | maintained this temperature for 5 hours, and obtained the high molecular weight epoxy resin solution. The obtained resin had 90% of solid content, epoxy equivalent 3,000, and number average molecular weight 8,000.
[53] Next, after adding 630 parts of carboxyl group-containing acrylic resin solutions and 110 parts of ethylene glycol monobutyl ether of 36% of solid content obtained by the manufacture example 1 to 1,000 parts of the said epoxy resin solutions, and stirring and mixing uniformly, temperature was made into 85 degreeC 50 parts of deionized water and 60 parts of dimethylethanolamines were added, and it hold | maintained for 1 hour. Subsequently, 2,600 parts of deionized water was dripped over 1 hour, and the comparative aqueous coating composition which is a water dispersion of 25% of solid content, the resin acid value 36 mgKOH / g, the viscosity 3,000 mPas, and the particle diameter of 180 nm was obtained.
[54] Comparative Example 2
[55] In the reaction vessel, 1,800 parts of bisphenol A diglycidyl ether (epoxy equivalent about 190, number average molecular weight about 350, residual bisphenol A not detected), 1,487 parts of bisphenol A, 363 parts of diethylene glycol monobutyl ether and 50% tetra 1 part of aqueous methyl ammonium solution was added, it heated up at 140 degreeC under stirring, and this temperature was hold | maintained for 8 hours, and the high molecular weight epoxy resin solution was obtained. Obtained resin had 90% of solid content, epoxy equivalent 9,100, and number average molecular weight 5,500.
[56] Next, after adding 630 parts of carboxyl group-containing acrylic resin solution and 113 parts of ethylene glycol monobutyl ether of 36% of solid content obtained by the manufacture example 1 to 1,000 parts of said epoxy resin solutions, and stirring and mixing it uniformly, the temperature was made into 85 degreeC 18 parts of deionized water and 60 parts of dimethylethanolamines were added, and it hold | maintained for 1 hour. Next, 2,600 parts of deionized water was dripped over 1 hour, and the comparative aqueous coating composition which is a water dispersion of 25% of solid content, resin acid value 36 mgKOH / g, viscosity 800 mPas, and particle diameter 350nm was obtained.
[57] Performance Test of Aqueous Coating Compositions
[58] Each of the aqueous coating compositions obtained in Examples 1 to 3 and Comparative Examples 1 and 2 was spray-coated to a clean tin free steel having a thickness of 0.23 mm so as to have a dry coating film thickness of 10 μm, and 200 ° C. Various coating film performance tests were performed based on the following test method using the coating plate baked and hardened by baking for 3 minutes. In addition, the bisphenol A concentration in each aqueous coating composition was measured.
[59] Test Methods
[60] Gel fraction: It is the weight percentage (%) of the non-extraction coating film weight after extraction with respect to the coating film weight before extraction when the cured coating film is solvent-extracted under acetone reflux for 6 hours.
[61] Substrate Adhesion: A nylon film is sandwiched between two coated plates (150 mm x 5 mm) as the surface to be bonded, which is heated at 200 ° C. for 60 seconds, and then pressurized at 200 ° C. for 30 seconds. What fused the film to the coating film was made into the test piece. Next, the T-peel adhesive strength of this test piece was measured using the tensile tester ("Autograph AGS-500A", a brand name, Shimadzu Corporation make). Tensile conditions were 200 mm / min of tensile velocity at the temperature of 20 degreeC.
[62] Workability: The coating plate is cut into a size of 40 mm x 50 mm, two bent so that the coating film surface becomes the outer side, a 3 kg weight is dropped from the height of 42 cm in the bent portion, and then the length is 20 at the cutting part. The part up to the width of mm was immersed in 1% sodium chloride aqueous solution, and the electric current value at the time of energizing for 6 second by the voltage of 6.5V was measured. The smaller this current value, the better the workability.
[63] Corrosion resistance: The coating plate was cut into the size of 150 mm x 70 mm, the crosscut was put in the coating film so that it might reach a base material, and the salt spray test was done for 3 weeks using the coating plate. About the coating board after a test, it evaluated visually by the following reference | standard.
[64] A: Rust part from cut part is less than 2mm on one side,
[65] B: The rust from the cut part is less than 5mm in more than 2mm on one side,
[66] C: The rusty part from a cut part is 5 mm or more on one side.
[67] Acid resistance: The coating surface which sealed the back surface and the cut surface was evaluated visually about the coating surface after immersing in 10% aqueous hydrochloric acid solution at 20 degreeC for one week.
[68] A: No abnormality
[69] B: A little white flower appears.
[70] C: Whitening appears remarkably.
[71] Alkali resistance: The coating surface which sealed the back surface and the cut surface was evaluated visually about the coated surface after immersing in 10% of caustic soda aqueous solution at 20 degreeC for one week.
[72] A: No abnormality
[73] B: A little white flower appears.
[74] C: Whitening appears remarkably.
[75] Bisphenol A concentration: The concentration of bisphenol A in the aqueous coating composition when the aqueous coating composition obtained in each example is dissolved in tetrahydrofuran and analyzed by high performance liquid chromatography is indicated.
[76] Table 1 shows the test results.
[77] ExampleComparative example One23One2 Gel fraction (%)90.589.091.092.490.8 Adhesiveness of substrate (adhesive strength, kg / 5mm)3.022.503.723.653.60 Machinability (current value, mA)0.320.500.290.430.38 Corrosion resistanceAAAAA Acid resistanceAAAAA Alkali resistanceAAAAA Bisphenol A Concentration (ppm)Not detected402,000
[78] The aqueous coating composition of the present invention does not contain free bisphenols in the coating material by using a specific carboxyl group-containing polyester resin, a specific low molecular weight epoxy compound and a carboxyl group-containing acrylic resin as raw materials, and thus the problem of environmental hormones. Is resolved. Moreover, it is excellent in coating workability and also excellent in coating film performance, such as base material adhesiveness, workability, corrosion resistance, acid resistance, alkali resistance, and flavor.
[79] Therefore, it can use suitably for internal surfaces of cans, such as an edible can.

权利要求:
Claims (9)
[1" claim-type="Currently amended] Epoxy by esterifying a carboxyl group-containing polyester resin (a) having a number average molecular weight of 1,000 to 30,000 and an acid value of 5 to 200 mgKOH / g and a 1,2-epoxy group-containing low molecular weight epoxy compound (b) having a number average molecular weight of 1,200 or less Obtaining modified polyester resin (A),
The obtained epoxy modified polyester resin (A) is reacted with a carboxyl group-containing acrylic resin (c) to obtain a carboxyl group-containing acrylic modified polyester resin (B),
The aqueous coating composition obtained by neutralizing the obtained acrylic modified polyester resin (B) and disperse | distributing in an aqueous medium.
[2" claim-type="Currently amended] The method of claim 1,
The carboxyl group-containing polyester resin (a) has a number average molecular weight of 2,000 to 10,000 and an acid value of 20 to 150 mgKOH / g.
Aqueous coating composition
[3" claim-type="Currently amended] The method of claim 1,
The said low molecular weight epoxy compound (b) is an epoxy equivalent of 140-250 and a number average molecular weight of 250-900
Aqueous coating composition.
[4" claim-type="Currently amended] The method of claim 1,
The carboxyl group-containing polyester resin (a) and the low molecular weight epoxy compound (b) are esterified at a compounding ratio in which the epoxy group of the carboxyl group of the resin (a): the epoxy group of the compound (b) is 1: 2 to 1: 1 in molar ratio. To obtain an epoxy-modified polyester resin (A).
Aqueous coating composition.
[5" claim-type="Currently amended] The method of claim 1,
Epoxy equivalent of the said epoxy-modified polyester resin (A) is 2,000-10,000, and number average molecular weight is 4,000-100,000.
Aqueous coating composition.
[6" claim-type="Currently amended] The method of claim 1,
The said carboxyl group-containing acrylic resin (c) is thing of 100-500 mgKOH / g of acid value
Aqueous coating composition.
[7" claim-type="Currently amended] The method of claim 1,
The epoxy-modified polyester resin (A) and the carboxyl group-containing acrylic resin (c) are reacted at a blending ratio such that the resin (A) / resin (c) is 60/40 to 90/10 in a solid content weight ratio, thereby forming a polyester resin ( To obtain B)
Aqueous coating composition.
[8" claim-type="Currently amended] The method of claim 1,
The said carboxyl group-containing acrylic modified polyester resin (B) is an acid value of 15-200 mgKOH / g
Aqueous coating composition.
[9" claim-type="Currently amended] The method of claim 1,
Further containing a crosslinking agent
Aqueous coating composition.

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同族专利:

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公开号 | 公开日

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US6780902B2|2004-08-24|

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JP2001181564A|2001-07-03|

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US20030004230A1|2003-01-02|

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WO2001048105A1|2001-07-05|

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KR100573428B1|2006-04-26|

引用文献:

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公开号 | 申请日 | 公开日 | 申请人 | 专利标题

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法律状态:
1999-12-27|Priority to JPJP-P-1999-00371398

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1999-12-27|Priority to JP37139899A

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2000-12-21|Application filed by 간사이 페인트 가부시키가이샤

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2002-08-14|Publication of KR20020065913A

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2006-04-26|Application granted

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2006-04-26|Publication of KR100573428B1

优先权:

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申请号 | 申请日 | 专利标题

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JPJP-P-1999-00371398|1999-12-27|

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JP37139899A|JP2001181564A|1999-12-27|1999-12-27|Water-based coating composition|