JP5669299B2 - Coating composition with excellent corrosion resistance - Google Patents

Description

  The present invention relates to a non-chromium coating composition having excellent corrosion resistance and a coated metal plate using the same, and more specifically, not only the corrosion resistance of the flat portion of the coated metal plate, but also the coating film is photodegraded or hydrolyzed in an outdoor environment. The present invention relates to a coating composition that is effective for improving the corrosion resistance of a processed part and an end face part even when deterioration due to is progressing, and a coated metal plate using the same.

  Conventionally, pre-coated metal sheets such as pre-coated steel sheets painted by coil coating, etc., building materials such as roofs, walls, shutters, garages, various household appliances, switchboards, refrigerated showcases, steel furniture, kitchen appliances, etc. Widely used as a housing related product.

  In order to manufacture these housing-related products from a pre-coated metal plate, the pre-coated steel plate is usually cut, press-molded and joined. Therefore, these housing-related products often have a metal exposed portion that is a cut surface and a crack generating portion due to press working. The exposed metal part and cracking part are more likely to have a lower corrosion resistance than other parts, so it is common to include a chromium-based rust-preventive pigment in the precoat steel base coat to improve corrosion resistance. Has been done.

  However, chromium-based anticorrosive pigments contain or produce hexavalent chromium having excellent antirust properties, and this hexavalent chromium is a problem from the viewpoint of human health and environmental protection. .

  To date, many non-chromium anticorrosive pigments such as zinc phosphate, aluminum tripolyphosphate, and zinc molybdate have been put on the market, and various primers have been proposed as a combination of non-chromium pigments. ing. For example, Patent Document 1 discloses a combination of epoxy resin and phenol resin vehicle components, a combination of calcium silicate and phosphorus vanadate, and a combination of calcium carbonate, calcium silicate, aluminum phosphate, and phosphorus vanadate as antirust pigments. A paint containing a rust preventive pigment is described. Patent Document 2 describes a paint in which polyester is combined with a combination of a second magnesium phosphate and a fired product of manganese oxide / vanadium oxide or a fired product of calcium phosphate and vanadium oxide as a rust preventive pigment. Yes. However, the coating film formed from the paint described in Patent Documents 1 and 2 is inferior in corrosion resistance as compared with a paint using a chromium pigment, and in particular, the corrosion resistance in the processed part and the end face part is insufficient. . In addition, chemical resistance such as alkali resistance and acid resistance is often inferior. Further, when a large amount of rust preventive pigment is used, the water resistance is often inferior, and it has not yet been replaced by chromium-based rust preventive pigments in the production of precoated metal sheets.

  Patent Document 3 discloses that a vehicle component composed of an organic resin containing a hydroxyl group or an epoxy group and a curing agent has an oil absorption of 30 to 200 ml / 100 g and a pore volume of 0.05 to 1.2 ml / g. A coating composition containing a silica fine particle and having a glass transition temperature of 40 to 125 ° C. of a cured coating film formed from the coating is described. However, although the coating film formed from the paint described in Patent Document 3 shows considerable corrosion resistance, it is still inferior in corrosion resistance and chemical resistance compared to a paint using a chromium-based pigment. Insufficient corrosion resistance.

  Further, Patent Document 4 discloses a coating composition containing a hydroxyl group-containing film-forming resin, a crosslinking agent and a rust preventive pigment mixture, wherein the rust preventive pigment mixture contains a specific vanadium compound, silica fine particles, and phosphoric acid series. A coating composition with excellent corrosion resistance is described which is composed of metal salts (metal salts such as calcium, zinc, aluminum, magnesium salts, etc.) and exhibits excellent corrosion resistance, but corrosion reaction after overcoating deteriorates due to outdoor exposure In terms of resistance to corrosion, that is, maintenance of corrosion resistance, further improvement and improvement of corrosion resistance have been demanded.

Japanese Patent Laid-Open No. 11-61001 JP 2000-199078 A JP 2000-129163 A JP 2008-222833 A

  The object of the present invention is not only the corrosion resistance of the general part in the painted metal plate etc., but also the corrosion resistance of the processed part and the end face part is excellent even when the coating film is deteriorated by photolysis or hydrolysis in the outdoor environment. The object is to provide a non-chromium coating composition capable of forming a coating film and a coated metal plate using the same.

  Therefore, as a result of intensive studies to solve the above-described conventional problems, the present inventors have identified a hydroxyl group-containing film-forming resin system as a phosphate group-containing resin and / or a phosphate group-containing resin. With a coating composition containing a predetermined amount of vanadium compound and an anti-rust pigment of ion-exchange silica, the coating composition has excellent corrosion resistance not only on the flat surface but also on the processed and end surfaces of painted metal sheets in an outdoor environment. The inventors have found that a film can be formed and have completed the present invention.

That is, the present invention comprises (A) a film-forming resin that does not contain a phosphate group but contains a hydroxyl group, (B) a crosslinking agent, (C) a rust preventive pigment mixture, and (D) a phosphate group-containing resin and / or A coating composition containing a phosphate group-containing resin (hereinafter sometimes abbreviated as “phosphoric acid (salt) group-containing resin (D)”), wherein the antirust pigment mixture (C) is (1 ) It consists of at least one vanadium compound of vanadium pentoxide, calcium vanadate and ammonium metavanadate and (2) ion-exchanged silica, and is a total solid content of the resin (A) and the crosslinking agent (B). For 100 parts by mass
3 to 50 parts by mass of the vanadium compound (1),
The amount of the ion exchange silica (2) is 3 to 50 parts by mass, and the total amount of the phosphoric acid (salt) group-containing resin (D) is 1 to 30 parts by mass, and the antirust pigment mixture (C ) Is 6 to 100 parts by mass, to provide a coating composition.

  Moreover, this invention provides the coating metal plate by which the cured coating film based on the said coating composition is formed on the metal plate in which the chemical conversion treatment may be performed on the surface.

  Furthermore, the present invention provides a composite film in which a cured coating film based on the coating composition is formed on a metal plate whose surface may be subjected to chemical conversion treatment, and a top coating film is formed on the cured coating film. A coated metal plate having a layer coating film is provided.

  Moreover, this invention provides the coating metal plate by which the cured coating film based on the said coating composition is formed on both surfaces of the metal plate in which the chemical conversion treatment may be performed on the surface.

  Further, in the present invention, a cured coating film based on the coating composition is formed on both surfaces of a metal plate that may be subjected to chemical conversion treatment on the surface, and a top coat is applied on the cured coating film on at least one surface. The present invention provides a coated metal plate having a multilayer coating film formed with a film.

The coating composition of the present invention does not contain a chromium-based rust preventive pigment and is a coating composition that is advantageous in terms of environmental hygiene. By the coating composition of the present invention, not only is the corrosion resistance of the flat part improved, It exhibits the effect of being able to form a coating film with excellent corrosion resistance at the processed and end surfaces of a coated metal plate that has been difficult to achieve with non-chromium anticorrosive paints. The coating composition of the present invention contains a phosphoric acid (salt) group-containing resin (D) and functions as a strong adhesion imparting component in an acidic atmosphere. The excellent adhesion imparting property, together with the specific vanadium compound and ion-exchanged silica that are rust preventive pigments, is considered to greatly contribute to the improvement of corrosion resistance over time in an outdoor environment.
That is, according to the present invention, the vanadium compound (1) and the ion exchange silica can be used not only for the corrosion resistance of the flat portion of the coated metal plate, but also for the coating film that has deteriorated due to photolysis or hydrolysis in an outdoor environment. (2) In addition to the action of the antirust pigment mixture (C) component comprising effectively covering the exposed surface of the material, the phosphoric acid (salt) group-containing resin (D) component is strong in an acidic atmosphere. Coating composition effective for improving the corrosion resistance of processed parts and end face parts by having an action of suppressing coating film peeling at the anode electrode in the vicinity of the corrosion-promoting part and a coated metal using the same A board is provided.

  The coated metal plate on which the cured coating film based on the coating composition of the present invention is formed has excellent corrosion resistance at the flat portion, processed portion and end face portion, and uses a conventional chromate rust preventive pigment such as strontium chromate. It has a corrosion resistance equal to or higher than that of a coated metal plate on which a cured coating film based on a paint is formed.

  A coated metal plate in which a cured coating film based on the coating composition of the present invention is formed, and a top coating film is formed on the cured coating film, is excellent in the corrosion resistance of the flat portion, the processed portion, and the end surface portion. When a galvanized steel plate or an aluminum-zinc alloy plated steel plate is used as the metal plate to be coated, it is excellent not only in the flat portion but also in the end face portion and the processed portion by applying the coating composition of the present invention. Corrosion resistance can be obtained.

  The paint composition of the present invention comprises the following hydroxyl group-containing film-forming resin (A), crosslinking agent (B), antirust pigment mixture (C), and phosphoric acid (salt) group-containing resin (D). It is a thing.

Hydroxyl-containing film-forming resin (A)
The hydroxyl group-containing coating film-forming resin in the coating composition of the present invention can be used without particular limitation as long as it is a hydroxyl group-containing resin having a coating film-forming ability that can be usually used in the paint field. , Polyester resin, epoxy resin, acrylic resin, fluororesin, vinyl chloride resin and the like can be used. As the film-forming resin, among them, at least one organic resin selected from a hydroxyl group-containing polyester resin and an epoxy resin can be preferably used.

  Examples of the hydroxyl group-containing polyester resin include oil-free polyester resins, oil-modified alkyd resins, and modified products of these resins such as urethane-modified polyester resins, urethane-modified alkyd resins, epoxy-modified polyester resins, and acrylic-modified polyester resins. Is done. The hydroxyl group-containing polyester resin has a number average molecular weight of 1,500 to 35,000, preferably 2,000 to 25,000, a glass transition temperature (Tg point) of 10 to 100 ° C., preferably 20 to 80 ° C., and a hydroxyl value. Those having 2-100 mg KOH / g, preferably 5-80 mg KOH / g are suitable.

  In the present specification, the “number average molecular weight” of the resin is a value calculated based on the molecular weight of standard polystyrene from a chromatogram measured by gel permeation chromatograph (“HLC8120GPC” manufactured by Tosoh Corporation). The column used was “TSKgel G-4000HXL”, “TSKgel G-3000HXL”, “TSKgel G-2500HXL”, “TSKgel G-2000HXL” (both manufactured by Tosoh Corporation, trade name), and moved. Phase: Tetrahydrofuran, Measurement temperature: 40 ° C., Flow rate: 1 cc / min, Detector: Under the conditions of RI. Moreover, in this specification, the glass transition temperature (Tg) of resin is based on a differential thermal analysis (DSC).

  The oil-free polyester resin is an esterified product of a polybasic acid component and a polyhydric alcohol component. Examples of the polybasic acid component include one or more selected from phthalic anhydride, isophthalic acid, terephthalic acid, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, succinic acid, fumaric acid, adipic acid, sebacic acid, maleic anhydride, and the like. Dibasic acids and lower alkyl esterified products of these acids are mainly used, and if necessary, monobasic acids such as benzoic acid, crotonic acid, pt-butylbenzoic acid, trimellitic anhydride, methylcyclohexentricarboxylic acid , Tribasic or higher polybasic acids such as pyromellitic anhydride are used in combination. Examples of the polyhydric alcohol component include bivalent compounds such as ethylene glycol, diethylene glycol, propylene glycol, 1,4-butanediol, neopentyl glycol, 3-methylpentanediol, 1,4-hexanediol, and 1,6-hexanediol. Alcohol is mainly used, and a trihydric or higher polyhydric alcohol such as glycerin, trimethylolethane, trimethylolpropane, pentaerythritol can be used in combination as necessary. These polyhydric alcohols can be used alone or in admixture of two or more. The esterification or transesterification reaction of both components can be carried out by a method known per se. As the acid component, isophthalic acid, terephthalic acid, and lower alkyl esterified products of these acids are particularly preferable.

  In addition to the acid component and alcohol component of the oil-free polyester resin, the alkyd resin is obtained by reacting an oil fatty acid by a method known per se. Examples of the oil fatty acid include coconut oil fatty acid, soybean oil fatty acid, Examples thereof include linseed oil fatty acid, safflower oil fatty acid, tall oil fatty acid, dehydrated castor oil fatty acid, and kiri oil fatty acid. The oil length of the alkyd resin is preferably 30% or less, particularly about 5 to 20%.

  As the urethane-modified polyester resin, the oil-free polyester resin or the low-molecular weight oil-free polyester resin obtained by reacting an acid component and an alcohol component used in the production of the oil-free polyester resin, a polyisocyanate compound and Examples thereof include those reacted by a method known per se. The urethane-modified alkyd resin is obtained by reacting the alkyd resin or a low molecular weight alkyd resin obtained by reacting each component used in the production of the alkyd resin with a polyisocyanate compound by a method known per se. Things are included. Polyisocyanate compounds that can be used in the production of urethane-modified polyester resins and urethane-modified alkyd resins include hexamethylene diisocyanate, isophorone diisocyanate, xylylene diisocyanate, tolylene diisocyanate, 4,4′-diphenylmethane diisocyanate, 4,4 ′. -Methylenebis (cyclohexyl isocyanate), 2,4,6-triisocyanatotoluene and the like. In general, as the urethane-modified resin, those having a modification degree such that the amount of the polyisocyanate compound forming the urethane-modified resin is 30% by weight or less with respect to the urethane-modified resin can be preferably used.

  As an epoxy-modified polyester resin, a polyester resin produced from each component used in the production of the polyester resin is used, a reaction product of a carboxyl group of the resin and an epoxy group-containing resin, a hydroxyl group in the polyester resin and an epoxy resin. The reaction product by reaction, such as addition of a polyester resin and an epoxy resin, condensation, grafting, etc., such as the product which couple | bonded the hydroxyl group in it through the polyisocyanate compound, can be mentioned. In general, the degree of modification in the epoxy-modified polyester resin is preferably such that the amount of the epoxy resin is 0.1 to 30% by weight with respect to the epoxy-modified polyester resin.

  As the acrylic-modified polyester resin, a polyester resin produced from each component used in the production of the polyester resin is used, and a group having reactivity with these groups on the carboxyl group or hydroxyl group of the resin, for example, carboxyl group, hydroxyl group or epoxy. Reaction products obtained by graft polymerization of a (meth) acrylic acid or (meth) acrylic acid ester to a polyester resin using a peroxide polymerization initiator are listed. be able to. In general, the degree of modification in the acrylic-modified polyester resin is preferably such that the amount of the acrylic resin is 0.1 to 50% by weight with respect to the acrylic-modified polyester resin.

  Of the polyester resins described above, among them, oil-free polyester resins and epoxy-modified polyester resins are preferable from the viewpoint of balance such as processability and corrosion resistance.

  Examples of the epoxy resin suitable as the hydroxyl group-containing coating film-forming resin include bisphenol-type epoxy resins, novolac-type epoxy resins; and modified epoxy resins in which various modifiers are reacted with epoxy groups or hydroxyl groups in these epoxy resins. be able to. In the production of the modified epoxy resin, the modification time with the modifier is not particularly limited, and it may be modified in the middle of the epoxy resin production or in the final stage of the epoxy resin production.

  The bisphenol-type epoxy resin is, for example, a resin obtained by condensing epichlorohydrin and bisphenol to a high molecular weight in the presence of a catalyst such as an alkali catalyst, if necessary, epichlorohydrin and bisphenol, and if necessary, an alkali catalyst or the like. Any of resins obtained by condensing into a low molecular weight epoxy resin in the presence of a catalyst and polyaddition reaction of the low molecular weight epoxy resin and bisphenol may be used.

  Examples of the bisphenol include bis (4-hydroxyphenyl) methane [bisphenol F], 1,1-bis (4-hydroxyphenyl) ethane, 2,2-bis (4-hydroxyphenyl) propane [bisphenol A], 2, 2-bis (4-hydroxyphenyl) butane [bisphenol B], bis (4-hydroxyphenyl) -1,1-isobutane, bis (4-hydroxy-tert-butyl-phenyl) -2,2-propane, p- (4-hydroxyphenyl) phenol, oxybis (4-hydroxyphenyl), sulfonylbis (4-hydroxyphenyl), 4,4′-dihydroxybenzophenone, bis (2-hydroxynaphthyl) methane, etc. Bisphenol A and bisphenol F are preferably used . The bisphenols can be used alone or as a mixture of two or more.

  Examples of commercially available products of bisphenol type epoxy resins include, for example, jER828, 812, 815, 820, 834, 1001, 1004, 1007, 1009, 1010 manufactured by Japan Epoxy Resin; Asahi Ciba Examples include Araldite AER6099 manufactured by the company, and Epomic R-309 manufactured by Mitsui Chemicals.

  Examples of the novolac type epoxy resin which is an epoxy resin suitable as a hydroxyl group-containing coating film-forming resin include, for example, phenol novolac type epoxy resins, cresol novolac type epoxy resins, and phenol glyoxal type epoxy having a large number of epoxy groups in the molecule. Various novolak-type epoxy resins such as resins can be mentioned.

  Examples of the modified epoxy resin include an epoxy ester resin obtained by reacting, for example, a dry oil fatty acid with the bisphenol type epoxy resin or the novolac type epoxy resin; and a polymerizable unsaturated monomer component containing acrylic acid or methacrylic acid. Epoxy acrylate resin; Urethane-modified epoxy resin reacted with isocyanate compound; Amino group or quaternary by reacting amine compound with epoxy group in bisphenol type epoxy resin, novolac type epoxy resin or various modified epoxy resins An amine-modified epoxy resin obtained by introducing an ammonium salt can be used.

Cross-linking agent (B)
The crosslinking agent (B) reacts with the hydroxyl group-containing coating film forming resin (A) to form a curing film, and reacts with the hydroxyl group-containing coating film forming resin (A) by heating or the like to be cured. However, amino resins, phenol resins and polyisocyanate compounds which may be blocked are particularly suitable. These crosslinking agents can be used alone or in combination of two or more.

  Examples of the amino resin include methylolated amino resins obtained by reacting an amino component such as melamine, urea, benzoguanamine, acetogranamamine, steroguanamine, spiroguanamine, and dicyandiamide with an aldehyde. Examples of the aldehyde used in the reaction include formaldehyde, paraformaldehyde, acetaldehyde, and benzaldehyde. Moreover, what etherified the said methylolated amino resin with suitable alcohol can also be used as an amino resin. Examples of alcohols used for etherification include methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, isobutyl alcohol, 2-ethylbutanol, 2-ethylhexanol and the like.

  The phenol resin that can be used as the cross-linking agent is one that undergoes a cross-linking reaction with the hydroxyl group-containing coating film-forming resin (A). The phenol component and formaldehyde are heated in the presence of a reaction catalyst to cause a condensation reaction, and methylol. Examples thereof include a resol type phenol resin obtained by alkylating a part or all of the methylol group of a methylolated phenol resin obtained by introducing a group with an alcohol.

  In the production of a resol-type phenol resin, a bifunctional phenol compound, a trifunctional phenol compound, a tetrafunctional or higher functional phenol compound, or the like can be used as the phenol component as a starting material.

  Examples of the phenol compound include, for example, bifunctional phenol compounds such as o-cresol, p-cresol, p-tert-butylphenol, p-ethylphenol, 2,3-xylenol, and 2,5-xylenol. Examples of the trifunctional phenol compound include carboxylic acid, m-cresol, m-ethylphenol, 3,5-xylenol, and m-methoxyphenol. Examples of the tetrafunctional phenol compound include bisphenol A and bisphenol F. Can be mentioned. Among them, in order to improve scratch resistance, it is preferable to use a trifunctional or higher functional phenol compound, in particular, carboxylic acid and / or m-cresol. These phenol compounds may be used alone or in combination of two or more.

  Examples of formaldehydes used in the production of phenol resins include formaldehyde, paraformaldehyde, trioxane, and the like, which can be used alone or in combination of two or more.

  As the alcohol used for alkyl etherifying a part of the methylol group of the methylolated phenol resin, a monohydric alcohol having 1 to 8 carbon atoms, preferably 1 to 4 carbon atoms, can be suitably used. Suitable monohydric alcohols include methanol, ethanol, n-propanol, n-butanol, isobutanol and the like.

  The phenol resin has an average of 0.5 or more, preferably 0.6 to 3.0 alkoxymethyl groups per benzene nucleus from the viewpoint of reactivity with the hydroxyl group-containing film-forming resin (A). What you have is suitable.

  Examples of the non-blocked polyisocyanate compound in the optionally-blocked polyisocyanate compound that can be used as the crosslinking agent include aliphatic diisocyanates such as hexamethylene diisocyanate or trimethylhexamethylene diisocyanate; hydrogenated xylylene diisocyanate or Cycloaliphatic diisocyanates such as isophorone diisocyanate; organic diisocyanates per se such as tolylene diisocyanate, xylylene diisocyanate or 4,4′-diphenylmethane diisocyanate, aromatic diisocyanates such as crude MDI, or each of these organic diisocyanates and polyvalent Adducts with alcohol, low molecular weight polyester resin or water, or as described above Cyclic polymerization of an organic diisocyanate comrades, further include isocyanate-biuret, or the like.

  The blocked polyisocyanate compound is obtained by blocking free isocyanate groups of the polyisocyanate compound with a blocking agent. Examples of the blocking agent include phenols such as phenol, cresol and xylenol; ε-caprolactam; lactones such as δ-valerolactam and γ-butyrolactam; methanol, ethanol, n-, i- or t-butyl alcohol, ethylene Alcohols such as glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monoethyl ether, propylene glycol monomethyl ether, and benzyl alcohol; oximes such as formamidoxime, acetaldoxime, acetoxime, methyl ethyl ketoxime, diacetyl monooxime, benzophenone oxime, cyclohexane oxime System: Active methylene such as dimethyl malonate, diethyl malonate, ethyl acetoacetate, acetylacetone It can be suitably used blocking agent, such as. By mixing the polyisocyanate compound and the blocking agent, free isocyanate groups of the polyisocyanate compound can be easily blocked.

  The blending ratio of the hydroxyl group-containing film-forming resin (A) and the crosslinking agent (B) is based on the total solid content of 100 parts by weight of the components (A) and (B), and the hydroxyl group-containing film-forming resin. (A) is 55 to 95 parts by weight, more preferably 60 to 95 parts by weight, and the crosslinking agent (B) is in the range of 5 to 45 parts by weight, further 5 to 40 parts by weight. It is suitable in terms of boiling water, processability, curability and the like.

  In order to increase the curability of the coating composition of the present invention, a curing catalyst can be blended as necessary. When the crosslinking agent (B) contains an amino resin, particularly a low molecular weight, methyl etherified or mixed etherified melamine resin of methyl ether and butyl ether, sulfonic acid compound or amine neutralization of sulfonic acid compound as a curing catalyst A thing is used suitably. Representative examples of the sulfonic acid compound include p-toluenesulfonic acid, dodecylbenzenesulfonic acid, dinonylnaphthalenesulfonic acid, dinonylnaphthalenedisulfonic acid, and the like. The amine in the amine neutralized product of the sulfonic acid compound may be any of primary amine, secondary amine, and tertiary amine. Among these, the amine neutralized product of p-toluenesulfonic acid and / or the amine neutralized product of dodecylbenzenesulfonic acid is preferable from the viewpoints of the stability of the coating, the reaction promoting effect, and the physical properties of the obtained coating film. .

  When the crosslinking agent (B) is a phenol resin, the sulfonic acid compound or an amine neutralized product of the sulfonic acid compound is suitably used as the curing catalyst.

  When the crosslinking agent (B) is a blocked polyisocyanate compound, a curing catalyst that promotes dissociation of the blocking agent of the blocked polyisocyanate compound, which is a curing agent, is suitable. As a suitable curing catalyst, for example, octyl Tin oxide, dibutyltin di (2-ethylhexanoate), dioctyltin di (2-ethylhexanoate), dioctyltin diacetate, dibutyltin dilaurate, dibutyltin oxide, dioctyltin oxide, lead 2-ethylhexanoate And organometallic catalysts such as

  When the crosslinking agent (B) is a combination of two or more kinds of crosslinking agents, an effective curing catalyst can be used in combination with each crosslinking agent.

Antirust pigment mixture (C)
In the coating composition of the present invention, the rust preventive pigment mixture (C) is composed of the following (1) vanadium compound and (2) ion exchange silica.

Vanadium compound (1)
The vanadium compound (1) is at least one vanadium compound selected from vanadium pentoxide, calcium vanadate, and ammonium metavanadate. Vanadium pentoxide, calcium vanadate and ammonium metavanadate are excellent in elution of pentavalent vanadium ions into water, and the pentavalent vanadium ions released from the vanadium compound (1) react with the material metal, It works effectively to improve corrosion resistance by reacting with ions from other antirust pigment mixtures.

Ion exchange silica (2)
The ion exchange silica (2) is a silica fine particle in which a cation such as calcium ion is introduced into a fine porous silica carrier by ion exchange. Examples of the ion exchange silica include calcium ion exchange silica, magnesium ion exchange silica, and cobalt ion exchange silica.

  As the ion exchange silica (2), silica fine powder having an average particle diameter of 0.5 to 15 μm, preferably 1 to 10 μm, and the oil absorption is in the range of 30 to 300 ml / 100 g, preferably 30 to 150 ml / 100 g. A thing can be used conveniently.

  As the ion exchange silica (2), calcium ion exchange silica is particularly preferable. Examples of commercially available calcium ion-exchanged silica include SHIELDEX (Shieldex, registered trademark) C303, AC-3, and C-5 (all of which are manufactured by WR Grace & Co.).

  Cations such as calcium ions released from ion-exchanged silica are involved in electrochemical action and various salt forming actions, and effectively work to improve corrosion resistance. Moreover, the silica fixed in the coating film effectively works to suppress peeling of the coating film in a corrosive atmosphere.

Phosphoric acid (salt) group-containing resin (D)
Of the phosphoric acid (salt) group-containing resin (D), the phosphoric acid group-containing resin is a phosphoric acid group [—OPO (OH) (OR ¹ )] (where R ¹ is a hydrogen atom, a phenyl group, or a carbon number of 1). To 20 alkyl groups, particularly preferably a hydrogen atom and 2 to 10 alkyl groups.) As for the type of resin, the hydroxyl group-containing film-forming resin (A) and the crosslinking agent (B ) Is not particularly limited, and examples thereof include phosphoric acid group-containing acrylic resins, phosphoric acid group-containing epoxy resins, and phosphoric acid group-containing polyester resins.

  The phosphoric acid group-containing acrylic resin can be obtained, for example, by copolymerizing a phosphoric acid group-containing unsaturated monomer and another polymerizable unsaturated monomer.

  Examples of the phosphate group-containing unsaturated monomer include (2-acryloyloxyethyl) acid phosphate, (2-methacryloyloxyethyl) acid phosphate, (2-acryloyloxypropyl) acid phosphate, (2-methacryloyloxypropyl) Acid phosphate, 10-acryloyloxydecyl acid phosphate, (meth) acryloyloxyalkyl (carbon number 2 to 20) acid phosphate such as 10-methacryloyloxydecyl acid phosphate; orthophosphoric acid and acidic phosphate (1 to 20 carbon atoms) To which is added an equimolar amount of an epoxy group-containing unsaturated monomer such as glycidyl (meth) acrylate; Kayamar PM-2, PM-21 (Nippon Kayaku Co., Ltd., trade name) and the like. Examples of the acidic phosphate ester include methyl acid phosphate, butyl acid phosphate, 2-ethylhexyl acid phosphate, isodecyl acid phosphate, lauryl acid phosphate, isotridecyl acid phosphate, oleyl acid phosphate, and phenyl acid phosphate. It is done.

  Examples of the other polymerizable unsaturated monomer that copolymerizes with the phosphoric acid group-containing unsaturated monomer constituting the phosphoric acid group-containing acrylic resin include, for example, 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl. Hydroxyl group-containing unsaturated monomers such as (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 2-hydroxyethyl vinyl ether, 2-hydroxypropyl vinyl ether, 2-hydroxyethyl allyl ether; acrylic acid, methacrylic acid; styrene, Vinyl aromatic compounds such as α-methylstyrene, vinyltoluene, α-chlorostyrene; methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, i-propyl (meth) acrylate, (n- I-, t-) butyl (meth) acrylate, Hexyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, isobornyl (meth) C1-C24 alkyl ester or cycloalkyl ester of acrylic acid or methacrylic acid such as acrylate; vinyl acetate, vinyl chloride, vinyl ether, acrylonitrile, methacrylonitrile and the like. In the present invention, “(meth) acrylate” means “acrylate or methacrylate”.

  In addition, phosphoric acid group-containing acrylic resin is obtained by adding a phosphoric acid compound to a copolymer resin of an unsaturated monomer having an epoxy group such as glycidyl (meth) acrylate and the above-mentioned other polymerizable unsaturated monomer. It can also be obtained by the method of As the phosphoric acid compound to be added, orthophosphoric acid, acidic phosphoric acid ester and the like are suitable, and examples of the acidic phosphoric acid ester include those exemplified as the acidic phosphoric acid ester.

  The phosphoric acid group-containing epoxy resin can be obtained by adding a phosphoric acid compound to an epoxy resin. Examples of the epoxy resin to which the phosphoric acid compound is added include, for example, bisphenol type epoxy resins, novolak type epoxy resins, and modified epoxy resins in which various modifiers are reacted with epoxy groups or hydroxyl groups in these epoxy resins. Can do. The type of phosphoric acid compound to be added is phosphoric acid to be added to a copolymer resin of an unsaturated monomer having an epoxy group and another polymerizable unsaturated monomer in the description of the phosphoric acid group-containing acrylic resin. What was mentioned as a system compound can be used similarly.

  The phosphoric acid group-containing polyester resin can be obtained, for example, by reacting a phosphoric acid compound with the hydroxyl group of the polyester resin. As the kind of the phosphoric acid compound to be reacted, those mentioned as the phosphoric acid compound in the description of the phosphoric acid group-containing acrylic resin can be used similarly.

  Among the phosphate (salt) group-containing resin (D), the phosphate group-containing resin can be obtained by reacting the phosphate group in the phosphate group-containing resin with a metal compound to form a phosphate. . Examples of the metal compound to be reacted with the phosphate group include calcium oxide, magnesium oxide, cobalt oxide, nickel oxide, zinc oxide, cerium oxide, and lanthanum oxide.

  The phosphoric acid group or phosphate group of the phosphoric acid (salt) group-containing resin (D) works effectively to improve adhesion imparting properties and corrosion resistance in an acidic atmosphere.

  In the coating composition of the present invention, the vanadium compound (1) and the ion exchange silica (C), which are the antirust pigment mixture (C), with respect to 100 parts by mass of the total solid content of the resin (A) and the crosslinking agent (B) 2), and the amount of the phosphoric acid (salt) group-containing resin (D) is in the following range, and the amount of the anticorrosive pigment mixture (C) is 6 to 100 parts by mass, preferably 10 to 60 parts by mass. It is preferable from the viewpoint of corrosion resistance.

Vanadium compound (1): 3 to 50 parts by mass, preferably 5 to 40 parts by mass,
Ion exchange silica (2): 3 to 50 parts by mass, preferably 3 to 30 parts by mass,
Phosphoric acid (salt) group-containing resin (D): 1 to 30 parts by mass, preferably 1 to 20 parts by mass.

  In the coating composition of the present invention, a predetermined amount of the vanadium compound (1), the ion-exchanged silica (2), and the phosphoric acid (salt) group-containing resin (D) is combined as the anticorrosive pigment mixture (C). In other words, the corrosion resistance can be improved synergistically.

  Moreover, each of the vanadium compound (1) and ion-exchange silica (2) which comprise the antirust pigment mixture (C) mix | blended with respect to 100 mass parts of total solid content of the said resin (A) and a crosslinking agent (B). The mixture of each part by mass of the pigment was added to 10000 parts by mass of a 5% strength by weight sodium chloride aqueous solution at 25 ° C., stirred for 6 hours, and the pH of the filtrate obtained by filtering the supernatant that was allowed to stand at 25 ° C. for 48 hours was 3-8, preferably 5-8 is preferred from the viewpoint of the solubility of the vanadium compound (1) and the ion-exchanged silica (2) with moisture and the reactivity between the solution of the rust preventive pigment and the metal plate. In this range, it is more preferable from the viewpoint of corrosion resistance.

  That is, the filtrate for measuring pH is ion-exchanged in any amount within the range of 3 to 50 parts by mass of the vanadium compound (1) with respect to 10000 parts by mass of a 5% by mass sodium chloride aqueous solution at 25 ° C. This is a filtrate of a solution obtained by adding and dissolving silica (2) in any amount within the range of 3 to 50 parts by mass.

  In the coating composition of the present invention, the hydroxyl group-containing coating film-forming resin (A), the crosslinking agent (B), the rust preventive pigment mixture (C), the phosphoric acid (salt) group-containing resin (D), and as necessary. In addition to the curing catalyst to be blended, color pigments, extenders, UV absorbers, UV stabilizers, organic solvents that can be used in the paint field, additives such as anti-settling agents, antifoaming agents, and coating surface conditioners are required. It can be blended accordingly.

  Examples of the colored pigment include organic colored pigments such as cyanine blue, cyanine green, organic red pigments such as azo and quinacridone; and inorganic colored pigments such as titanium white, titanium yellow, bengara, carbon black, and various fired pigments. Among them, titanium white can be preferably used.

  Examples of the extender pigment include talc, clay, mica, alumina, calcium carbonate, barium sulfate and the like.

  Examples of the ultraviolet absorber include 2- (2-hydroxy-3,5-di-t-amylphenyl) -2H-benzotriazole, isooctyl-3- (3- (2H-benzotriazol-2-yl)- 5-t-butyl-4-hydroxyphenylpropionate, 2- [2-hydroxy-3,5-di (1,1-dimethylbenzidine) phenyl] -2H-benzotriazole, 2- [2-hydroxy-3- Dimethylbenzyl-5- (1,1,3,3-tetramethylbutyl) phenyl] -2H-benzotriazole, methyl-3- [3-t-butyl-5- (2H-benzotriazol-2-yl)- Benzotriazole derivatives such as condensates with 4-hydroxyphenyl] propionate / polyethylene glycol 300; 2- [4- (2-hydroxy Triazine derivatives such as 3-dodecyloxypropyl) oxy] -2-hydroxyphenyl-4,6-bis (2,4-dimethylphenyl) -1,3,5-triazine; ethanediamide-N- (2-ethoxyphenyl) ) -N ′-(2-ethylphenyl)-(oxalic amide), ethanediamide-N- (2-ethoxyphenyl) -N ′-(4-isododecylphenyl)-(oxalic amide), etc. Derivatives and the like can be mentioned.

  Examples of the ultraviolet stabilizer include, for example, hindered amine compounds, hindered phenol compounds; CHIMASORB 944, TINUVIN 144, TINUVIN 292, TINUVIN 770, IRGANOX 1010, IRGANOX 1098. Product)).

  By blending UV absorbers and UV stabilizers in the paint, it is possible to suppress the deterioration of the coating surface due to light. Even when this paint is used as a primer, it passes through the upper coating film and becomes a primer. Since the deterioration of the primer surface due to the light reaching the coating surface can be suppressed, delamination between the primer coating and the upper coating due to the deterioration of the primer coating surface can be prevented, and excellent corrosion resistance can be maintained.

  The said organic solvent which can be mix | blended with this invention coating composition is mix | blended as needed for the coating property improvement of this invention composition, etc., and a hydroxyl-containing film-forming resin (A) and a crosslinking agent ( B) which can dissolve or disperse can be used. Specifically, for example, hydrocarbon solvents such as toluene, xylene and high boiling petroleum hydrocarbons, ketone solvents such as methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and isophorone Ester solvents such as ethyl acetate, butyl acetate, ethylene glycol monoethyl ether acetate, diethylene glycol monoethyl ether acetate, alcohol solvents such as methanol, ethanol, isopropanol, butanol, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, And ether alcohol-based solvents such as ethylene glycol monobutyl ether can be cited, which may be used alone or in combination of two or more.

  In the coating composition of the present invention, the glass transition temperature of the cured coating film obtained from the composition of the present invention is 40 to 115 ° C, preferably 50 to 105 ° C, such as the corrosion resistance, acid resistance and workability of the coating film. To preferred. The glass transition temperature of the coating film was tan δ by temperature dispersion measurement at a frequency of 110 Hz using a DINAMIC VISCOELASTOMETER MODEL VIBRON (dynamic viscoelastometer model vibron) DDV-IIEA type (manufactured by Toyo Baldwin, automatic dynamic viscoelasticity measuring machine). It is the maximum temperature obtained from the change in.

The coating film formed by coating the coating composition of the present invention on a metal plate exhibits excellent corrosion resistance. The reason for this is that the present inventors have developed metal ions and pentavalent vanadium ions (VO ₃ ⁻ and VO ₄ ³⁻ vanadate ions) generated by dissolution of the raw material metal by chloride ions and the like in a corrosive environment. The direct formation of precipitating salt without the redox reaction of trivalent vanadium ions and raw metal ions generated by the redox reaction between pentavalent vanadium ions and the raw material metal It is considered that the first reason is to effectively cover the exposed surface of the material by effectively producing a precipitating salt or compound with the cation or silicate ion released by hydrolysis.

  In addition, the ion exchange silica has a strong effect of adjusting the pH of the wet atmosphere in the vicinity thereof to weakly acidic by the effect of the weakly acidic functional group on the surface as well as the effect of the cation released in the corrosive atmosphere. Promotes the oxidation-reduction reaction between the vanadium ions and the material metal, and the ion-exchanged silica is immobilized on the coating film, so that it can adjust pH even in the long-term corrosive atmosphere. It is considered that the second reason is that it persists or sustains hydrolysis in a sacrificial manner under a stronger corrosive atmosphere and releases silicate ions.

  Furthermore, in the coated steel sheet, the top coat film becomes hydrophilic due to deterioration, and various corrosion promoting factors are considered to pass through the flat surface of the top coat film. However, the phosphoric acid (salt) group-containing resin (D) is acidic. Since it acts as a strong adhesion-imparting component in the atmosphere, it suppresses coating film peeling at the anode electrode in the vicinity of the corrosion progressing part, and effectively neutralizes hydroxyl groups generated by oxygen reduction reaction at the cathode electrode, and its pH Is considered to be the third reason.

  In addition, the phosphate group based on the phosphoric acid (salt) group-containing resin (D) adjusts the pH of the atmosphere so that vanadate ions and silicate ions can suitably perform various reactions and salt formation on the metal surface. It is considered that there is an effect of maintaining weak acidity. It is believed that a very high level of corrosion resistance has been achieved by a combination of these various mechanisms.

Furthermore, by using the vanadium compound (1), the ion-exchange silica (2) and the phosphoric acid (salt) group-containing resin (D) constituting the rust preventive pigment mixture (C), the vanadium compound (1), Each of the ion exchange silica (2) and the phosphoric acid (salt) group-containing resin (D) can effectively counteract the weak acid resistance, alkali resistance and water resistance. It is thought that the synergistic effect of the action based on these rust preventive pigment mixture (C) and phosphoric acid (salt) group-containing resin (D) worked greatly, and excellent corrosion resistance was achieved.
That is, according to the present invention, the vanadium compound (1) and the ion exchange silica can be used not only for the corrosion resistance of the flat portion of the coated metal plate, but also for the coating film that has deteriorated due to photolysis or hydrolysis in an outdoor environment. (2) In addition to the action of the antirust pigment mixture (C) component comprising effectively covering the exposed surface of the material, the phosphoric acid (salt) group-containing resin (D) component is strong in an acidic atmosphere. Coating composition effective for improving the corrosion resistance of processed parts and end face parts by having an action of suppressing coating film peeling at the anode electrode in the vicinity of the corrosion-promoting part and a coated metal using the same A board is provided.

Painted metal plate The coating composition of the present invention can obtain a painted metal plate by coating and curing on a metal plate. As the metal plate to be coated, cold rolled steel plate, hot dip galvanized steel plate, electrogalvanized steel plate, iron-zinc alloy plated steel plate (galvanyl steel plate), aluminum-zinc alloy plated steel plate (containing about 55% aluminum in the alloy) Metal plate such as “galvanium steel plate”, “galfan” containing about 5% aluminum in the alloy), nickel-zinc alloy plated steel plate, stainless steel plate, aluminum plate, copper plate, copper plated steel plate, tin plated steel plate, etc. The surface of the metal plate may be subjected to chemical conversion treatment. Examples of the chemical conversion treatment include phosphate treatment such as zinc phosphate treatment and iron phosphate treatment, composite oxide film treatment, chromium phosphate treatment, and chromate treatment.

  The composition of the present invention can be coated on the metal plate by a known method such as a roll coating method, a curtain flow coating method, a spray method, a brush coating method, or a dipping method. Although the cured film thickness of the coating film obtained from this invention composition is not specifically limited, Usually, 2-10 micrometers, Preferably it is used in the range of 3-6 micrometers. Curing of the coating film may be appropriately set according to the type of resin used, etc., and when the material coated by the coil coating method is continuously baked, the material reached maximum temperature is usually 160 to 250 ° C. It is preferably baked for 15 to 60 seconds under the condition of 180 to 230 ° C. In the case of baking in a batch system, it can be carried out by baking at 80 to 200 ° C. for 10 to 30 minutes. In addition, when a non-blocked polyisocyanate is used as the crosslinking agent (B), or when a bisphenol type epoxy resin is used as the resin (A) and an amine compound is used as the crosslinking agent (B), a coating film forming process In the case of a combination that does not particularly require heating for the crosslinking reaction in, it can be cured by drying at room temperature according to a conventional method.

  The coated metal plate of the present invention has a coating film formed of the above-described coating composition of the present invention on a metal plate which may be subjected to chemical conversion treatment, and the coated metal plate formed with the coating film of the present coating composition The coating itself can be used, but a top coating film can also be provided on this coating film. The film thickness of the top coat film is usually 8 to 30 μm, preferably 10 to 25 μm.

  Examples of the top coating for forming the top coating film include, for example, top coatings such as polyester resin-based, alkyd resin-based, silicon-modified polyester resin-based, silicon-modified acrylic resin-based, and fluororesin-based coatings that are known for pre-coated steel sheets. Can do. When workability is particularly important, a coated steel sheet having particularly excellent workability can be obtained by using a polyester-based top coat for advanced processing. The coated metal plate of this invention can show the coating-film performance excellent in corrosion resistance.

  When using a galvanized steel plate or an aluminum-zinc alloy plated steel plate as the metal plate to be coated, the corrosion resistance of the flat surface has been considerably improved. Although the corrosion resistance was insufficient, by applying the coating composition of the present invention, excellent corrosion resistance can be obtained also in the end face part and the processed part.

  Moreover, the coating film by this invention coating composition may be provided in both surfaces of to-be-coated article, and the said top coating film is further formed on the coating film by this invention coating composition as needed. May be. By forming the coating composition of the present invention on both sides, that is, on the back side, it is possible to obtain a coated metal plate that does not contain a chromium-based rust preventive pigment and is advantageous in terms of environmental hygiene and excellent in corrosion resistance.

  Hereinafter, the present invention will be described more specifically with reference to production examples and examples. The present invention is not limited to the following examples. Hereinafter, “parts” and “%” are based on mass.

Production Example 1 Production of resol type phenolic resin crosslinker solution In a reaction vessel, 100 parts of bisphenol A, 178 parts of 37% formaldehyde aqueous solution and 1 part of sodium hydroxide were blended and reacted at 60 ° C. for 3 hours. Dehydrated at 0 ° C. for 1 hour. Then, 100 parts of n-butanol and 3 parts of phosphoric acid were added and reacted at 110 to 120 ° C. for 2 hours. After completion of the reaction, the resulting solution was filtered to remove sodium phosphate, which was obtained to obtain a resol type phenolic resin crosslinking agent solution B1 having a solid content of about 50%. The obtained resin had a number average molecular weight of 880, an average number of methylol groups per benzene nucleus of 0.4, and an average number of alkoxymethyl groups of 1.0.

Production Example 2 Production of paint for back surface 80 parts of jER1009 (Japan epoxy resin, bisphenol A type epoxy resin, hydroxyl group-containing resin) mixed solvent 1 [cyclohexanone / ethylene glycol monobutyl ether / solvesso 150 (Esso Petroleum, high boiling point) (Aromatic hydrocarbon solvent) = 3/1/1 (mass ratio)] In 200 parts of an epoxy resin solution dissolved in 120 parts, 40 parts of titanium white, 40 parts of varita, and a mixed solvent 2 [Solvesso 150 (manufactured by Esso Oil Co., Ltd.) , High-boiling aromatic hydrocarbon solvent) / cyclohexanone = 1/1 (mass ratio)] was mixed, and pigment dispersion was performed until the tube (particle diameter of the coarse pigment particles) became 20 microns or less. Next, 26.7 parts (20 parts by solid content) of Desmodur BL-3175 (manufactured by Sumika Bayer Urethane Co., Ltd., HDI isocyanurate type polyisocyanate compound solution blocked with methyl ethyl ketoxime, solid content of about 75%) was added to this dispersion. ), Takenate TK-1 (manufactured by Takeda Pharmaceutical Co., Ltd., organotin blocking agent dissociation catalyst, solid content of about 10%), and uniformly mixed, and further mixed solvent 2 and viscosity of about 80 seconds (Ford Cup # 4/25 ° C.) to obtain a back coating material.

Production of phosphoric acid (salt) group-containing resin Production Example 3 Production of phosphoric acid group-containing acrylic resin 1 A reactor vessel was charged with 100 parts of butanol, and the monomer raw materials and the like were mixed in advance while maintaining the reaction vessel temperature at 110 ° C. The mixture having the following composition was added dropwise over 3 hours.

Styrene 50 parts 2-Ethylhexyl methacrylate 35 parts Glycidyl methacrylate 15 parts 2,2'-azobisisobutyronitrile 2.0 parts Then, 0.5 parts of 2,2'-azobisisobutyronitrile is added. The reaction was carried out at 110 ° C. for 2 hours. Next, the temperature in the reaction vessel is set to 80 ° C., 12.2 parts of orthophosphoric acid having a concentration of 85% and 10.4 parts of butanol are gradually added, and the reaction is carried out for 1 hour until the reaction vessel is free of turbidity. % Phosphoric acid group-containing acrylic resin 1 solution was obtained. The phosphoric acid group-containing acrylic resin 1 which is a solid content had a resin acid value of 54 (0.096 equivalent / 100 g resin in terms of phosphoric acid group concentration).

Production Example 4 Production of Phosphoric Acid Group-Containing Acrylic Resin 2 Into a reaction vessel, 100 parts of butanol was added, and while maintaining the temperature in the reaction vessel at 110 ° C., a mixture having the following composition mixed in advance with monomer raw materials was added dropwise over 3 hours. did.

Styrene 53 parts 2-Ethylhexyl methacrylate 40 parts Glycidyl methacrylate 7 parts 2,2'-azobisisobutyronitrile 2.0 parts Then, 0.5 parts of 2,2'-azobisisobutyronitrile is added. The reaction was carried out at 110 ° C. for 2 hours. Subsequently, the temperature in the reaction vessel is set to 80 ° C., 5.7 parts of orthophosphoric acid having a concentration of 85% and 4.9 parts of butanol are gradually added, and the reaction is performed for 1 hour until turbidity in the reaction vessel disappears. % Phosphoric acid group-containing acrylic resin 2 solution was obtained. The phosphoric acid group-containing acrylic resin 2 that is a solid content had a resin acid value of 26 (0.047 equivalent / 100 g resin in terms of phosphoric acid group concentration).

Production Example 5 Production of Phosphoric Acid Group-Containing Acrylic Resin 3 Into a reaction vessel, 100 parts of butanol was added, and while maintaining the temperature in the reaction vessel at 110 ° C., a mixture having the following composition mixed in advance with monomer raw materials was added dropwise over 3 hours. did.

Styrene 40 parts 2-ethylhexyl methacrylate 30 parts glycidyl methacrylate 30 parts 2,2'-azobisisobutyronitrile 2.0 parts Then, 0.5 parts of 2,2'-azobisisobutyronitrile is added. The reaction was carried out at 110 ° C. for 2 hours. Next, the temperature in the reaction vessel is set to 80 ° C., 25 parts of orthophosphoric acid having a concentration of 85% and 17 parts of butanol are gradually added, and the reaction is performed for 1 hour until the reaction vessel is free of turbidity. A group-containing acrylic resin 3 solution was obtained. The phosphoric acid group-containing acrylic resin 3, which is a solid content, had a resin acid value of 98 (0.17 equivalent / 100 g resin in terms of phosphoric acid group concentration).

Production Example 6 Production of Phosphate Group-Containing Epoxy Resin In a reaction vessel, 100 parts of cyclohexanone and 100 parts of jER1007 (Japan Epoxy Resin Co., Ltd., bisphenol A type epoxy resin, hydroxyl group-containing resin) were charged, stirred and heated to 70 ° C. The resin was dissolved. Subsequently, 5.76 parts of 85% orthophosphoric acid was added and reacted at 70 ° C. for 2 hours, and then 4 parts of cyclohexanone was added to obtain a 50% phosphoric acid group-containing epoxy resin solution. The phosphoric acid group-containing epoxy resin, which is a solid content, had a resin acid value of 28 (0.05 equivalent / 100 g resin in terms of phosphoric acid group concentration).

Production Example 7 Production of phosphate group-containing acrylic resin In a sturdy glass container, 100 parts (50 parts in solids) of acrylic resin solution 1 having a solid content of 50% obtained in Production Example 3 and calcium oxide ground in a mortar 5 parts was mixed, filled with glass beads, and dispersed with a scan dix (trade name, agitator manufactured by Mitsuwa Tech Co., Ltd.) until the resin solution became transparent. Then, it was left at room temperature for 48 hours. Thereafter, the glass beads were removed to obtain a target phosphate group-containing acrylic resin solution.

Production of Ion Exchange Silica Production Example 8 Production of Mg Ion Exchange Silica 10 parts by mass of Silicia 710 (manufactured by Fuji Silysia Chemical Co., Ltd., trade name, silica fine particles, oil absorption amount in 10000 parts by mass of magnesium chloride aqueous solution having a concentration of 5% by mass About 105 ml / 100 g) was stirred and mixed for 5 hours and then filtered to take out the solid content. The solid content was thoroughly washed with water and dried to obtain Mg ion-exchanged silica.

Production Example 9 Production of Co ion-exchanged silica 10 parts by mass of Silicia 710 (manufactured by Fuji Silysia Chemical Co., Ltd., trade name, silica fine particles, oil absorption of about 105 ml / 100 g) in 10000 parts by mass of 5% by weight cobalt chloride aqueous solution After stirring and mixing for 5 hours, the solid content was filtered out, the solid content was washed well with water and dried to obtain Co ion-exchanged silica.

Example 1 Production of Rust-Preventing Paint Composition
jER1009 (Japan Epoxy Resin, bisphenol A type epoxy resin, hydroxyl group-containing resin) 85 parts mixed solvent 1 [cyclohexanone / ethylene glycol monobutyl ether / Sorvesso 150 (Esso Petroleum, high boiling aromatic hydrocarbon solvent) = 3/1/1 (mass ratio)] 225 parts of an epoxy resin solution dissolved in 135 parts, 5 parts of vanadium pentoxide, Shieldex AC-3 (manufactured by WR Grace & Co., trade name, Calcium 3 parts of ion exchange silica), 20 parts of titanium white, 20 parts of barita and mixed solvent 2 [Solvesso 150 (manufactured by Esso Petroleum Corporation, high boiling aromatic hydrocarbon solvent) / cyclohexanone = 1/1 (mass ratio)] The amounts were mixed, and the pigment was dispersed until the tub (particle diameter of the coarse pigment particles) became 20 microns or less. Next, Desmodur BL-3175 (manufactured by Sumika Bayer Urethane Co., Ltd., HDI isocyanurate type polyisocyanate compound solution blocked with methyl ethyl ketoxime, about 75% solid content) in this dispersion was 20 parts (15 parts in solid content), 4 parts of a phosphoric acid group-containing acrylic resin solution obtained in Production Example 3 (2 parts in terms of solid content), Takenate TK-1 (manufactured by Takeda Pharmaceutical Co., Ltd., organotin blocking agent dissociation catalyst, solid content of about 10%) 2 parts Was added and mixed uniformly, and the mixed solvent 2 was further added to adjust the viscosity to about 80 seconds (Ford Cup # 4/25 ° C.) to obtain a rust preventive coating composition.

Example 2-16, Comparative Examples 1 to 10 and Reference Examples 1 and 2
In Example 1, except that the hydroxyl group-containing resin, crosslinking agent, rust preventive pigment, and other pigments used were as shown in Table 1 below, the same procedure as in Example 1 was performed to obtain each rust preventive coating composition. Reference Examples 1 and 2 are rust preventive coating compositions containing conventional chromate rust preventive pigments. The amounts of the hydroxyl group-containing resin, the crosslinking agent, the phosphoric acid (salt) group-containing resin, and the pigment component in Table 1 are all expressed in terms of solid mass. However, in Example 15, Takenate not TK-1 is blended, also Oite in Example 16, in place of Takenate TK-1 2 parts Nacure 5225 (US King Industries Izu Co., dodecyl 1 part of an amine neutralized solution of benzenesulfonic acid) is blended.

  Table 1 shows the amount of each rust preventive pigment (C) and the amount of strontium chromate with respect to the resin components (total solid content of 100 parts by mass of the hydroxyl group-containing resin and the crosslinking agent). The pH of the filtrate obtained by filtering the supernatant liquid added to 10,000 parts by mass, stirred for 6 hours and allowed to stand at 25 ° C. for 48 hours is also described. For example, the pH of the rust preventive pigment solution of Example 1 is obtained by adding 5 parts by mass of vanadium pentoxide and 3 parts by mass of Shieldex AC-3 to 10000 parts by mass of a 5% by mass sodium chloride aqueous solution at 25 ° C. It is pH of the filtrate which filtered the supernatant liquid dissolved on the said conditions.

In Table 1 above, (Note) in the table has the following meanings.
(Note 1) Epokey 837: manufactured by Mitsui Chemicals, Inc., trade name, urethane-modified epoxy resin, hydroxyl group-containing resin, primary hydroxyl value of about 35, acid value of about 0.
(Note 2) Byron 296: manufactured by Toyobo Co., Ltd., trade name, epoxy-modified polyester resin, hydroxyl group-containing resin, hydroxyl value 7, acid value 6.
(Note 3) Sumidur N3300: manufactured by Sumika Bayer Urethane Co., Ltd., isocyanurate type polyisocyanate compound, solid content 100%.
(Note 4) Cymel 303: Nihon Cytec Industries, Ltd., trade name, methyl etherified melamine resin.
(Note 5) Shieldex C303: W.W. R. Grace & Co. Product name, calcicum ion exchange silica.
(Note 6) Aerosil 200: manufactured by Nippon Aerosil Co., Ltd., trade name, silica fine particles, oil absorption of about 280 ml / 100 g.
(Note 7) sandvor 3058: manufactured by Clariant, trade name, hindered amine UV stabilizer.

Preparation of test coating plate Using the anticorrosion paint composition and the top coating obtained in Examples 1 to 16 and Comparative Examples 1 to 10 and Reference Examples 1 and 2, each material was coated with the following coating specifications. Baking was performed to obtain a test plate for each test.

Paint specification 1:
Chemically treated galvalume steel sheet (thickness 0.35 mm, aluminum-zinc alloy plated steel sheet, containing about 55% aluminum in alloy, alloy plating basis weight 150 g / m ² , indicated as “GL steel sheet” in Table 2 )), The back coating material obtained in Production Example 2 was applied with a bar coater to a dry film thickness of 8 μm, and the back coating film was baked for 30 seconds so that the maximum material temperature reached 180 ° C. Formed. On the steel plate surface opposite to the back surface coating film of the coated plate on which this back surface coating film was formed, each rust preventive coating composition obtained in each of the above examples was coated with a bar coater so as to have a dry film thickness of 5 μm. Each primer coating was formed by baking for 40 seconds so that the maximum temperature reached 220 ° C. After cooling, KP color 1580B40 (trade name, polyester-based top coating, blue, glass transition temperature of cured coating about 70 ° C.) is applied to these primer coatings with a bar coater. The coating was applied to a thickness of about 15 μm, and baked for 40 seconds so that the maximum material temperature reached 220 ° C., to obtain a test plate for each test.

Paint specification 2:
On the hot-dip galvanized steel sheet subjected to chemical conversion treatment (plate thickness 0.35 mm, galvanized basis weight 250 g / m ² , indicated as “GI steel sheet” in Table 2), the coating for the back surface obtained in Production Example 2 Was coated with a bar coater so as to have a dry film thickness of 8 μm, and baked for 30 seconds so that the maximum material reaching temperature was 180 ° C. to form a back coating film. On the steel plate surface opposite to the back surface coating film of the coated plate on which this back surface coating film was formed, each rust preventive coating composition obtained in each of the above examples was coated with a bar coater so as to have a dry film thickness of 5 μm. Each primer coating plate was obtained by baking for 40 seconds so that the maximum temperature reached 220 ° C. After cooling, KP color 1580B40 (trade name, polyester-based top coating, blue, glass transition temperature of cured coating film of about 70 ° C.) is dried on these primer coating plates with a bar coater. The coating was applied to a thickness of about 15 μm, and baked for 40 seconds so that the maximum material temperature reached 220 ° C., to obtain a test plate for each test.

Paint specification 3:
The same anticorrosive paint composition obtained in Example 3 was applied to the same galvalume steel plate as used in the coating specification 1 with a bar coater so as to have a dry film thickness of 8 μm, so that the maximum material temperature reached 180 ° C. Then, it was baked for 30 seconds to form a back coating film. On the steel plate surface opposite to the back surface coating film of the coated plate on which this back surface coating film was formed, each rust preventive coating composition obtained in each of the above examples was coated with a bar coater so as to have a dry film thickness of 5 μm. Each primer coating was formed by baking for 40 seconds so that the maximum temperature reached 220 ° C. After cooling, KP color 1580B40 (trade name, polyester-based top coating, blue, glass transition temperature of cured coating about 70 ° C.) is applied to these primer coatings with a bar coater. The coating was applied to a thickness of about 15 μm, and baked for 40 seconds so that the maximum material temperature reached 220 ° C., to obtain a test plate for each test.

Coating Film Performance Test A coating film performance test was performed on each of the test coating plates obtained in Examples 1 to 16 and Comparative Examples 1 to 10 and Reference Examples 1 and 2 according to the following test method. The test results are shown in Table 2 below.

Test method Boiling water resistance: After each test coating plate cut to a size of 5 cm × 10 cm is immersed in boiling water at about 100 ° C. for 5 hours, it is pulled up to evaluate the appearance of the coating film on the surface side, and a cross-cut tape An adhesion test was performed and evaluated. The cross-cut tape adhesion test is based on JIS K-5400 8.5.2 (1990) cross-cut tape method, the gap interval of the cuts is 1 mm, 100 cross-cuts are made, and cellophane adhesive tape is adhered to the surface. And the number of grids remaining on the coated surface after abrupt peeling was examined.

A: There is no abnormality such as blistering or whitening in the coating film, and there are 100 remaining grids,
○: There are no abnormalities such as blistering and whitening in the coating film, and a residual grid number of 91 to 99,
Δ: Slightly abnormalities such as blistering or whitening were observed in the coating film and the number of residual grids was 91 or more, or there were no abnormalities such as blistering or whitening in the coating film, but the remaining grids were 71 to 90 Pieces,
X: Generation | occurrence | production of the swelling of a coating film is recognized fairly or remarkably, or the number of remaining grids is 70 or less.

  Alkali resistance: The back surface and the cut surface of each test paint plate cut to a size of 5 cm × 10 cm were sealed with a rust-proof paint, and a cross cut reaching the substrate was put in the center of the front side of the paint plate. This coated plate was immersed in a 5% aqueous sodium hydroxide solution at 40 ° C. for 48 hours, then taken out, washed, and evaluated for the appearance of the coating on the surface side of the coated plate dried at room temperature. Was peeled off, and the peel width (one side) from the cut portion in the coating film after peeling off was evaluated.

A: There is no occurrence of blisters, and the peel width from the cut part is 1.5 mm or less,
○: No occurrence of swelling, peeling width from cut part exceeds 1.5 mm, 3 mm or less,
Δ: Slight occurrence of swelling is observed, but tape peeling width from the cut portion is 3 mm or less, or occurrence of swelling is not recognized, but the tape peeling width from the cut portion exceeds 3 mm,
X: Generation | occurrence | production of a swelling is recognized and the tape peeling width from a cut part exceeds 3 mm.

  Acid resistance: The back surface and cut surface of each test paint plate cut to a size of 5 cm × 10 cm were sealed with a rust-proof paint, and a cross cut reaching the substrate was put in the center of the front side of the paint plate. This coated plate was immersed in a 5% sulfuric acid aqueous solution at 40 ° C. for 48 hours, then taken out, washed with water, and the appearance of the coating on the surface side of the coated plate dried at room temperature was evaluated, and a cellophane adhesive tape was adhered to the crosscut part. The peel width (one side) from the cut portion in the coating film after being peeled off rapidly was evaluated.

A: There is no occurrence of swelling, and the tape peeling width from the cut part is 1.5 mm or less.
○: There is no occurrence of swelling, and the tape peeling width from the cut part exceeds 1.5 mm and is 3 mm or less.
Δ: Slight occurrence of swelling is observed, but tape peeling width from the cut portion is 3 mm or less, or occurrence of swelling is not recognized, but the tape peeling width from the cut portion exceeds 3 mm,
X: Generation | occurrence | production of a swelling is recognized and the tape peeling width from a cut part exceeds 3 mm.

  Scratch resistance: Using a coin scratch tester (manufactured by Kayaku Giken Kogyo Co., Ltd.) at a room temperature of 20 ° C., keep the edge of the 10-yen copper coin at a 45 ° angle on the surface of each test coating plate, 3 kg The degree of scratching when the coated surface was scratched by pulling a 10-yen copper coin at a speed of 10 mm / second for about 30 mm while being pressed with a load of was evaluated according to the following criteria.

A: No metal substrate is seen on the scratched part.
○: A slight metal base is seen on the scratched part.
△: A considerable amount of metal base is seen in the scratched part,
X: A coating film is hardly left on the scratched part, and the metal base is clearly seen.

  Composite corrosion resistance test: Test specimens used for the composite corrosion resistance test are prepared as follows. Each test coating plate cut to a width of 7 cm x 15 cm in advance was subjected to an accelerated weathering test for 500 hours with a xenon accelerated weathering tester, and then cut with a shearing cutter at 5 mm from each end of the long side. Then, the burrs were cut so that the burrs faced to the front surface side on the right side and faced to the back side on the left side toward the surface-side coating surface. Insert a cross cut with a narrow angle of 30 degrees and a line width of 0.5 mm that reaches the substrate at the center of the front side of the test piece using the back of the cutter knife, and seal the upper edge of the paint plate with anticorrosive paint. 3T bend processing part (processing to bend with the front side of the paint plate on the outside, sandwich three sheets of the same thickness as the paint plate inside, and fold the paint plate 180 degrees in a vise) A test piece was prepared. Each obtained test piece was subjected to a combined cycle corrosion test according to JIS K-5621 (1990). The conditions of the combined cycle corrosion test are as follows: (5% saline sprayed at 30 ° C. for 0.5 hour)-(Test for 1.5 hours in a humidity tester with RH of 95% or higher at 30 ° C.)-(Dry at 50 ° C. for 2 hours) )-(Drying at 30 ° C. for 2 hours) is one cycle, and 200 cycles (total of 1200 hours) were tested. The state of the 3T bending process part, the edge part, the cross cut part, and the plane part of the test piece after this test was evaluated.

(3T bending process part) It evaluated on the following reference | standard by the total length of the rust part in 3T bending process part, and the presence or absence of generation | occurrence | production of red rust.
A: White rust is not recognized, or white rust is recognized, but less than 5 mm,
○: White rust is recognized but not less than 5 mm and less than 20 mm,
Δ: White rust is 20 mm or more and less than 40 mm,
X: Generation | occurrence | production of white rust 40 mm or more or red rust is recognized.

(Edge part) Evaluation was made according to the following criteria based on the average value of the edge creep widths on the left and right long sides of the test piece and the presence or absence of red rust.
A: There is no red rust, and the average edge creep width is less than 5 mm.
○: No occurrence of red rust, average value of edge creep width of 5 mm or more and less than 10 mm,
Δ: No occurrence of red rust, edge creep width average value of 10 mm or more and less than 20 mm,
X: The average value of edge creep width is 20 mm or more, or the occurrence of red rust is observed.

(Cross cut part) Corrosion state of the cross cut part of the test piece, white rust occurrence length ratio in the bare metal exposed part of 0.5mm cut width, average value of the left and right swelling width (sum of both sides) of the cut part In addition, it was evaluated according to the following criteria depending on whether red rust was generated.
A: White rust generation length ratio in exposed metal portion is less than 50% and swelling width is less than 3 mm,
○: The white rust generation length ratio in the bare metal exposed portion is 50% or more and less than 3 mm, or the white rust occurrence length ratio in the bare metal exposed portion is less than 50% and the swelling width is 3 mm or more and less than 5 mm,
Δ: White rust generation length ratio in exposed metal portion is 50% or more and swelling width is 5 mm or more and less than 10 mm,
X: White rust generation length ratio in the bare metal exposed portion is 50% or more, and a swelling width of 10 mm or more, or generation of red rust is observed.

(Plane part) The discontinuous and sporadic swelling of the plane part, which occurs at a part away from the tip of the corrosion part from the continuous edge, was evaluated according to the following criteria.
A: No occurrence of blistering is observed,
○: The diameter of the swelling is less than about 2 mm, and the number is less than 10,
Δ: The diameter of the bulge is approximately 2 mm or more and less than 10 pieces, or the bulge diameter is 2 mm.
Less than 10 pieces,
X: The bulge diameter is about 2 mm or more and the number is 10 or more.

Claims (11)

(A) A film-forming resin containing no hydroxyl group and containing a hydroxyl group, (B) a crosslinking agent, (C) a rust preventive pigment mixture, and (D) a phosphate group-containing resin and / or a phosphate group-containing resin A coating composition containing a phosphoric acid (salt) group-containing resin, wherein the antirust pigment mixture (C) is at least one of (1) vanadium pentoxide, calcium vanadate and ammonium metavanadate. Of the vanadium compound and (2) ion exchange silica, and with respect to 100 parts by mass of the total solid content of the resin (A) and the crosslinking agent (B),
3 to 50 parts by mass of the vanadium compound (1),
The amount of the ion exchange silica (2) is 3 to 50 parts by mass, and the total amount of the phosphate group-containing resin and the phosphate group-containing resin of the phosphate (salt) group-containing resin (D) is 1 to 30 parts by mass. And the quantity of this rust preventive pigment mixture (C) is 6-100 mass parts, The coating composition characterized by the above-mentioned. The coating composition according to claim 1, wherein the film-forming resin (A) is at least one of a hydroxyl group-containing epoxy resin and a hydroxyl group-containing polyester resin. The coating composition according to claim 1 or 2, wherein the crosslinking agent (B) is at least one crosslinking agent selected from an amino resin, a phenol resin, and a polyisocyanate compound which may be blocked. The coating composition according to any one of claims 1 to 3, wherein the ion exchange silica (2) is at least one of calcium ion exchange silica, magnesium ion exchange silica and cobalt ion exchange silica. Furthermore, the coating composition as described in any one of Claims 1-4 which contains at least 1 sort (s) of pigment component among a rust preventive pigment other than a rust preventive pigment mixture (C), a titanium dioxide pigment, and an extender pigment. object. Furthermore, the coating composition as described in any one of Claims 1-5 containing at least 1 sort (s) of a ultraviolet absorber and a ultraviolet stabilizer. Each of the pigments of the vanadium compound (1) and the ion exchange silica (2) constituting the rust preventive pigment mixture (C) blended with respect to 100 parts by mass of the total solid content of the resin (A) and the crosslinking agent (B). Each of the parts by weight of the mixture was added to 10000 parts by weight of a 5% strength by weight sodium chloride aqueous solution at 25 ° C., stirred for 6 hours, and allowed to stand at 25 ° C. for 48 hours. The coating composition according to claim 1, wherein the coating composition is a coating composition. The coated metal plate by which the cured coating film based on the coating composition of any one of Claims 1-7 is formed on the metal plate in which the chemical conversion treatment may be performed on the surface. A cured coating film based on the coating composition according to any one of claims 1 to 7 is formed on a metal plate that may be subjected to chemical conversion treatment on the surface, and an overcoat coating is formed on the cured coating film. A coated metal plate having a multilayer coating film formed with a film. The coated metal plate by which the cured coating film based on the coating composition of any one of Claims 1-7 is formed in both surfaces of the metal plate which may be subjected to chemical conversion treatment on the surface. A cured coating film based on the coating composition according to any one of claims 1 to 6 is formed on both surfaces of a metal plate that may be subjected to chemical conversion treatment on the surface, and at least one surface is cured. A coated metal plate having a multilayer coating film in which a top coating film is formed on the coating film.