JP5554608B2 - Metal pigment composition - Google Patents

Description

  The present invention relates to a coating composition or an ink composition, and more particularly to a metal pigment composition suitable for an aqueous coating composition or an aqueous ink.

In recent years, in the paint field, there has been an increasing need to switch to water-based paints that use less organic solvents as a resource-saving and pollution-free measure. However, metallic paints containing aluminum pigments are still practical. There are few examples of water-based paints.
The reason is that the aluminum pigment is easily corroded in the water-based paint and easily generates hydrogen gas. This is an extremely important safety issue in the coating process in paint manufacturers and in the painting process in automobile and home appliance manufacturers. In the following, the stability against corrosion of aluminum pigments in water-based paints is defined as “storage stability”.

  Patent Document 1 discloses an aluminum pigment treated with a treatment liquid containing an oxidizing agent composed of molybdic acid, tungstic acid and salts thereof, phosphate ions, and alkaline earth metal ions. Patent Document 2 discloses a metal pigment-containing paste obtained by treating metal pigment particles with a heteropolyanion such as phosphomolybdic acid or phosphotungstic acid. Moreover, in patent document 3, the metal particle paste which comprises the metal particle processed using the phosphomolybdate pigment was disclosed. However, according to the methods described in these prior documents, the color tone of the metal pigment is inevitably lowered. Patent Document 4 discloses a metal pigment composition containing a mixed coordination type heteropolyacid, but the storage stability is insufficient.

JP-A-4-318181 Japanese translation of PCT publication No. 8-502317 JP 2000-7939 A JP 2008-120932 A

  The present invention provides a metal pigment composition that overcomes the above-mentioned drawbacks of the prior art, that is, it can be used in paint compositions or ink compositions, particularly aqueous paints or aqueous inks, and has excellent storage stability, and It is an object of the present invention to provide a metal pigment composition in which the brightness, concealment, flip-flop feeling and the like are less reduced when formed into a coating film.

  The present inventors have excellent storage stability by using a metal pigment composition containing at least one heteropolyanion compound or mixed coordination heteropolyanion compound, inorganic phosphoric acid or a salt thereof, and a metal pigment. The present inventors have found that it is possible to obtain a metal pigment composition capable of achieving both good properties and excellent color tone, and have completed the present invention.

That is, the present invention is as follows.
(1) A metal pigment composition containing at least one heteropolyanion compound or mixed coordination heteropolyanion compound, inorganic phosphoric acid or a salt thereof, and a metal pigment.
(2) The metal pigment composition according to (1), wherein the metal pigment is aluminum flakes.
(3) The metal pigment composition according to (1) or (2), wherein the heteroatom constituting the heteropolyanion compound or the mixed coordination heteropolyanion compound is at least one selected from IIIB, IVB, and VB group elements. object.
(4) The metal pigment composition according to (3), wherein the IIIB, IVB, and VB group elements are B, Si, and P, respectively.
(5) The metal pigment composition according to any one of (1) to (4), wherein the poly atom constituting the heteropolyanion compound or the mixed coordination heteropolyanion compound is selected from transition metals.
(6) The metal pigment composition according to (5), wherein the transition metal is Ti, Zr, V, Nb, Mo, W.
(7) The heteropolyanion compound is H ₃ PMo ₁₂ O ₄₀ · nH ₂ O (phosphomolybdic acid · n hydrate), H ₃ PW ₁₂ O ₄₀ · nH ₂ O (phosphotungstic acid · n hydrate), _{H 4 SiMo 12 O 40 · nH} 2 O ( silicomolybdic acid · n-hydrate) and _{H 4 SiW 12 O 40 · nH} 2 O , at least one selected from the group consisting of (silicotungstic acid · n-hydrate) The metal pigment composition according to (1) or (2).
(8) mixed coordinated heteropolyanion _{compounds, H 3 PW x Mo 12-} x O 40 · nH 2 O ( phosphorus (tungsto) molybdic acid · _{n-hydrate), H 3 + x PV x} Mo 12-x O 40 NH ₂ O (phosphorus (vanado) molybdic acid n hydrate), H ₄ SiW _x Mo _12-x O ₄₀ nH ₂ O (silk (tungsto) molybdic acid n hydrate) and H _{4 + x} SiV _x The metal pigment composition according to (1) or (2), which is at least one selected from the group consisting of Mo _12-x O ₄₀ · nH ₂ O (silica (vanado) molybdic acid · n hydrate). (However, 1 ≦ x ≦ 11, n ≧ 0)
(9) Any of (1) to (7), wherein the heteropolyanion compound is a salt of a heteropolyanion constituting the heteropolyanion compound and one selected from the group consisting of alkali metals, alkaline earth metals, and ammonia A metal pigment composition according to claim 1.
(10) A salt in which the mixed coordination heteropolyanion compound is a mixed coordination heteropolyanion constituting the mixed coordination heteropolyanion compound and one selected from the group consisting of alkali metals, alkaline earth metals, and ammonia The metal pigment composition according to any one of (1) to (8),

（式中、Ｒ１、Ｒ２およびＲ３は同じでも異なってもよく、水素原子、または炭素原子数１から３０の、任意にエーテル結合、エステル結合、水酸基、カルボニル基、チオール基を含んでもよい１価もしくは２価の炭化水素基であり、任意にＲ１とＲ２は一緒になって５員もしくは６員のシクロアルキル基を形成するか、または任意にＲ１とＲ２は窒素原子と一緒になって、架橋員として付加的に窒素もしくは酸素原子を含むことができる５員もしくは６員環を形成するか、または任意にＲ１、Ｒ２およびＲ３は一緒になって、１個以上の付加的な窒素原子および／または酸素原子を架橋員として含むことができる多員の多重環組成物を形成する。Ｒ１、Ｒ２およびＲ３は同時に水素原子にはならない。ｎは１から２の数を表す。） (11) Any of (1) to (7), wherein the heteropolyanion compound is a salt of a heteropolyanion constituting the heteropolyanion compound and at least one selected from amine compounds represented by the following general formula (1) A metal pigment composition according to claim 1.

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.)

（式中、Ｒ１、Ｒ２およびＲ３は同じでも異なってもよく、水素原子、または炭素原子数１から３０の、任意にエーテル結合、エステル結合、水酸基、カルボニル基、チオール基を含んでもよい１価もしくは２価の炭化水素基であり、任意にＲ１とＲ２は一緒になって５員もしくは６員のシクロアルキル基を形成するか、または任意にＲ１とＲ２は窒素原子と一緒になって、架橋員として付加的に窒素もしくは酸素原子を含むことができる５員もしくは６員環を形成するか、または任意にＲ１、Ｒ２およびＲ３は一緒になって、１個以上の付加的な窒素原子および／または酸素原子を架橋員として含むことができる多員の多重環組成物を形成する。Ｒ１、Ｒ２およびＲ３は同時に水素原子にはならない。ｎは１から２の数を表す。） (12) A salt in which the mixed coordination type heteropolyanion compound is a mixed coordination type heteropolyanion constituting the mixed coordination type heteropolyanion compound and at least one selected from amine compounds represented by the following general formula (2) The metal pigment composition according to any one of (1) to (8).

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.)

(13) The inorganic phosphoric acid is at least one selected from orthophosphoric acid, metaphosphoric acid, pyrophosphoric acid, triphosphoric acid, tetraphosphoric acid, and phosphorous acid, (1) or (2) Metal pigment composition.

（式中、Ｒ１、Ｒ２およびＲ３は同じでも異なってもよく、水素原子、または炭素原子数１から３０の、任意にエーテル結合、エステル結合、水酸基、カルボニル基、チオール基を含んでもよい１価もしくは２価の炭化水素基であり、任意にＲ１とＲ２は一緒になって５員もしくは６員のシクロアルキル基を形成するか、または任意にＲ１とＲ２は窒素原子と一緒になって、架橋員として付加的に窒素もしくは酸素原子を含むことができる５員もしくは６員環を形成するか、または任意にＲ１、Ｒ２およびＲ３は一緒になって、１個以上の付加的な窒素原子および／または酸素原子を架橋員として含むことができる多員の多重環組成物を形成する。Ｒ１、Ｒ２およびＲ３は同時に水素原子にはならない。ｎは１から２の数を表す。） (14) The inorganic phosphate is a salt of inorganic phosphoric acid and one selected from the group consisting of an alkali metal, an alkaline earth metal, ammonia, and an amine represented by the following general formula (3) (1 Or the metal pigment composition according to (2).

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.)

(15) The metal pigment composition according to (13), wherein the inorganic phosphoric acid is at least one selected from the group consisting of orthophosphoric acid, metaphosphoric acid, and pyrophosphoric acid.

（式中、Ｒ４、Ｒ５、Ｒ６の少なくとも１つは、下記一般式（５）であり、他は水素原子または炭素数１から８の炭化水素基を表す。）

（式中、Ｒ７、Ｒ８、Ｒ９のうち少なくとも１つは炭素数６から２０の炭化水素基であり、他は水素原子または炭素数１から５の炭化水素基を表す。） (16) The inorganic phosphate portion of the inorganic phosphate is at least one selected from orthophosphoric acid, metaphosphoric acid, and pyrophosphoric acid, and the basic portion forming the salt is ammonia, morpholine, the following general formula (4), ( The metal pigment composition according to (14), which is at least one selected from ethanolamines represented by 5) or alkylamines represented by the following general formula (6).

(In the formula, at least one of R 4, R 5 and R 6 is the following general formula (5), and the other represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms.)

(In the formula, at least one of R7, R8, and R9 is a hydrocarbon group having 6 to 20 carbon atoms, and the other represents a hydrogen atom or a hydrocarbon group having 1 to 5 carbon atoms.)

(17) The metal pigment composition according to any one of (1) to (12), wherein the heteropolyanion compound or the mixed coordination heteropolyanion compound is present in an amount of 0.01 to 10 parts by weight with respect to 100 parts by weight of the metal pigment. .
(18) The metal pigment composition according to any one of (1) to (16), wherein the inorganic phosphoric acid or a salt thereof is present in an amount of 0.01 to 10 parts by weight with respect to 100 parts by weight of the metal pigment.
(19) Further, 0.01 to 5 parts by weight of at least one selected from an antioxidant, a light stabilizer and a polymerization inhibitor is contained in an amount of 0.01 to 5 parts by weight based on 100 parts by weight of the metal pigment. The metal pigment composition according to any one of

(20) The metal pigment composition according to any one of (1) to (19), further containing 0.01 to 30 parts by weight of a surfactant relative to 100 parts by weight of the metal pigment.
(21) The metal pigment is mixed in a separate step or the same step with a heteropolyanion compound or mixed coordination type heteropolyanion compound and inorganic phosphoric acid or a salt thereof in a solvent optionally containing water. ) To (18). The method for producing a metal pigment composition according to any one of (18).
(22) A coating composition comprising the metal pigment composition according to any one of (1) to (20).
(23) An ink composition comprising the metal pigment composition according to any one of (1) to (20).

  When the metal pigment composition of the present invention is used in a paint composition or ink composition, particularly an aqueous paint or water-based ink, it has a good storage stability and a coating film excellent in glitter, concealment and flip-flop. Can be obtained.

Hereinafter, the present invention will be described in detail with a focus on preferred embodiments.
As the metal pigment used in the present invention, base metal flakes such as aluminum, zinc, iron, magnesium, copper, and nickel, and alloy flakes thereof can be preferably used. Particularly suitable are aluminum flakes which are frequently used as metallic pigments. As the aluminum flakes used in the present invention, those having surface properties, particle sizes and shapes required for metallic pigments such as surface gloss, whiteness, and glitter are suitable.

  The shape is preferably scaly. Illustrating aluminum flakes, the average particle size (d50) is preferably 2 to 40 μm, the average thickness (t) is preferably in the range of 0.01 to 2 μm, and the average aspect ratio is in the range of 10 to 2500. Is preferred. Here, the average aspect ratio is a value obtained by dividing the average particle diameter (d50) of the aluminum flakes by the average thickness (t). Aluminum flakes are usually commercially available in a paste state, and these may be used, or the surface fatty acids may be removed in advance with an organic solvent or the like. A so-called aluminum vapor-deposited foil having an average particle diameter (d50) of 3 to 30 μm and an average thickness (t) of 5 to 50 nm can also be used.

The heteropolyanion compound or mixed coordination type heteropolyanion compound used in the present invention is composed of a group IIIB, IVB, or VB group element and one or two kinds of transition metal elements. The heteropolyanion is an oxoacid anion containing two or more kinds of central ions, and is distinguished from an isopolyanion having one kind of central ions. It has been found that most elements of the periodic table can be heteroatoms of a heteropolyanion.
To illustrate one of the most common structures of heteropoly anions for example, heteropolyanion typically composed of one type of transition metal element _{^{[X a + M b + 12}} O 2- 40] (80-a-12b) - Table is mixed coordinated heteropolyanion comprising two kinds of transition metals _{^{[X a + M b + x}} N c + 12-x O 2- 40] {80-a-bx-c (12-x)} - expressed in (Where X represents elements of group IIIB, IVB, VB such as B, Si, Ge, P, As, etc., and M, N represent transition metals such as Ti, Zr, V, Nb, Ta, Mo, W, etc.) Represents.)

Heteropolyanion compounds can have many structures, but typical heteropolyanion compounds include H ₃ PMo ₁₂ O ₄₀ · nH ₂ O (phosphomolybdic acid · n hydrate), H ₃ PW ₁₂ O ₄₀ · nH. ₂ O (phosphotungstic acid n hydrate), H ₄ SiMo ₁₂ O ₄₀ nH ₂ O (silicomolybdic acid n hydrate), H ₄ SiW ₁₂ O ₄₀ nH ₂ O (silicotungstic acid n Hydrate) and the like. Further, the mixing coordinated heteropolyanion _{compounds, H 3 PW x Mo 12-} x O 40 · nH 2 O ( phosphorus (tungsto) molybdic acid · _{n-hydrate), H 3 + x PV x} Mo 12-x O 40 NH ₂ O (phosphorus (vanado) molybdic acid n hydrate), H ₄ SiW _x Mo _12-x O ₄₀ nH ₂ O (silk (tungsto) molybdic acid n hydrate), H _{4 + x} SiV _x Examples thereof include Mo _12-x O ₄₀ · nH ₂ O (silica (vanado) molybdic acid · n hydrate). (However, 1 ≦ x ≦ 11, n ≧ 0)

Examples of the cation of the heteropolyanion used in the present invention include alkali metals such as potassium and sodium, alkaline earth metals such as calcium and magnesium, metals such as aluminum, zinc and manganese, ammonia, and amine compounds.
The amine compound is represented by the following general formula (7), and is a linear primary amine such as ethylamine, propylamine, butylamine, hexylamine, octylamine, laurylamine, tridecylamine, stearylamine; isopropylamine, isobutylamine Branched primary amines such as 2-ethylhexylamine and branched tridecylamine; direct amines such as dimethylamine, diethylamine, dipropylamine, dibutylamine, dihexylamine, dioctylamine, dilaurylamine, ditridecylamine and distearylamine. Chain secondary amines; branched secondary amines such as diisopropylamine, diisobutylamine, di-2-ethylhexylamine, branched ditridecylamine; methyl butylamine, ethyl butylamine, ethyl hexyl Asymmetric secondary amines such as amine, ethyl laurylamine, ethyl stearylamine, isopropyl octylamine, isobutyl 2-ethylhexylamine; trimethylamine, triethylamine, tripropylamine, tributylamine, trioctylamine, trilaurylamine, Linear tertiary amines such as tritridecylamine, tristearylamine; branched tertiary amines such as triisopropylamine, triisobutylamine, tri-2-ethylhexylamine, branched tritridecylamine; dimethyloctylamine, dimethyllaurylamine, Besides tertiary amines having mixed hydrocarbon groups such as dimethylstearylamine and diethyllaurylamine, allylamine, diallylamine, triallylamine, N, N-dimethyl Amine having an alkenyl group such as allylamine, alicyclic primary amine such as cyclohexylamine and 2-methylcyclohexylamine; primary amine having an aromatic ring substituent such as benzylamine and 4-methylbenzylamine; dicyclohexylamine, di-2 -Aliphatic secondary amines such as methylcyclohexylamine, secondary amines with aromatic ring substituents such as dibenzylamine, di-4-methylbenzylamine; cyclohexyl 2-ethylhexylamine, cyclohexyl benzylamine, stearyl Asymmetric secondary amines such as benzylamine and 2-ethylhexyl benzylamine; Alicyclic tertiary amines such as dimethylbenzylamine, dimethylcyclohexylamine and tricyclohexylamine; Tribenzylamine and tri-4-methylben Tertiary amines with aromatic ring substituents such as dilamine; morpholine, 3-methoxypropylamine, 3-ethoxypropylamine, 3-butoxypropylamine, 3-decyloxypropylamine, 3-lauryloxypropylamine, monoethanol Amine, diethanolamine, monoisopropanolamine, monopropanolamine, butanolamine, triethanolamine, N, N-dimethylethanolamine, N-methylethanolamine, N-methyldiethanolamine, N-ethylethanolamine, N-propylethanolamine, N-isopropylethanolamine, N-butylethanolamine, N-cyclohexyl-N-methylaminoethanol, N-benzyl-N-propylaminoethanol, or N-hydroxyl Ethylpyrrolidine, N-hydroxyethylpiperazine, N-hydroxyethylmorpholine, ethylenediamine, 1,2-propanediamine, 1,3-propanediamine, N, N-dimethyl-1,3-propanediamine, N-cyclohexyl-1, 3-propanediamine, N-decyl-1,3-propanediamine, N-isotridecyl-1,3-propanediamine, N, N-dimethylpiperazine, N-methoxyphenylpiperazine, N-methylpiperidine, N-ethylpiperidine, Examples include quinuclidine, diazabicyclo [2,2,2] octane, 1,8-diazabicyclo [5,4,0] -7-undecene, and the like, or a mixture thereof.

（式中、Ｒ１、Ｒ２およびＲ３は同じでも異なってもよく、水素原子、または炭素原子数１から３０の、任意にエーテル結合、エステル結合、水酸基、カルボニル基、チオール基を含んでもよい１価もしくは２価の炭化水素基であり、任意にＲ１とＲ２は一緒になって５員もしくは６員のシクロアルキル基を形成するか、または任意にＲ１とＲ２は窒素原子と一緒になって、架橋員として付加的に窒素もしくは酸素原子を含むことができる５員もしくは６員環を形成するか、または任意にＲ１、Ｒ２およびＲ３は一緒になって、１個以上の付加的な窒素原子および／または酸素原子を架橋員として含むことができる多員の多重環組成物を形成する。Ｒ１、Ｒ２およびＲ３は同時に水素原子にはならない。ｎは１から２の数を表す。） Among these, particularly preferred examples include stearylamine, di-2-ethylhexylamine, dioctylamine, linear or branched ditridecylamine, distearylamine, linear or branched tritridecylamine, tristearylamine, morpholine, 3- Examples include ethoxypropylamine, N, N-dimethylethanolamine, triethanolamine and the like.

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.)

  Examples of inorganic phosphoric acid used in the present invention include orthophosphoric acid, pyrophosphoric acid, metaphosphoric acid, triphosphoric acid, tetraphosphoric acid, phosphorous acid, polyphosphoric acid, lauryl phosphoric acid, polyoxypropylene oleyl ether phosphoric acid, dipoly Examples thereof include oxyethylene nonylphenyl ether phosphoric acid. Among these, orthophosphoric acid, pyrophosphoric acid, metaphosphoric acid, triphosphoric acid, tetraphosphoric acid, and phosphorous acid are particularly preferable.

（式中、Ｒ１、Ｒ２およびＲ３は同じでも異なってもよく、水素原子、または炭素原子数１から３０の、任意にエーテル結合、エステル結合、水酸基、カルボニル基、チオール基を含んでもよい１価もしくは２価の炭化水素基であり、任意にＲ１とＲ２は一緒になって５員もしくは６員のシクロアルキル基を形成するか、または任意にＲ１とＲ２は窒素原子と一緒になって、架橋員として付加的に窒素もしくは酸素原子を含むことができる５員もしくは６員環を形成するか、または任意にＲ１、Ｒ２およびＲ３は一緒になって、１個以上の付加的な窒素原子および／または酸素原子を架橋員として含むことができる多員の多重環組成物を形成する。Ｒ１、Ｒ２およびＲ３は同時に水素原子にはならない。ｎは１から２の数を表す。） Substances constituting the salt of inorganic phosphate used in the present invention include alkali metals such as potassium and sodium, alkaline earth metals such as calcium and magnesium, metals such as aluminum, zinc and manganese, ammonia, and the following general formula ( And amines represented by 8). Among these amines, ammonia, morpholine, N, N-dimethylethanolamine, triethanolamine and the like are particularly preferable examples.

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.)

  Moreover, as an antioxidant used for this invention, it is represented by the phenol type compound, the phosphorus type compound, and the sulfur type compound. Suitable compounds include 2,6-di-t-butylphenol, 2,4-dimethyl-6-t-butylphenol, butylhydroxytoluene (BHT), 2,6-di-t-butyl-4-ethyl-phenol. 2,4,6-tri-t-butylphenol, 2,6-di-t-butyl-4-s-butylphenol, butylhydroxyanisole (BHA), tocopherol, 2,6-di-t-butyl-4- Hydroxymethylphenol, n-octadecyl-β- (4′-hydroxy3′5′-di-t-butylphenyl) propionate, 2-t-butyl-4- (N, N-dimethylaminomethyl) phenol, 3, 5-di-t-butyl-4-hydroxybenzylphosphonate-diethyl ester, propyl gallate, octyl gallate, lauryl galley 2,2'-methylenebis (4-methyl-6-t-butylphenol), 2,2'-methylenebis (4-ethyl-6-t-butylphenol), 4,4'-methylenebis (2,6-di-) t-butylphenol), 2,2′-methylenebis (4-methyl-6-cyclohexylphenol), 2,2′-dihydroxy-3,3′-di (α-methylcyclohexyl) -5,5′-dimethyldiphenylmethane, 2,2′-dimethylene-bis- (6-α-methyl-benzyl-p-cresol), 2,2′-ethylidene-bis (4,6-di-t-butylphenol), 2,2′-butylidene- Bis (4-methyl-6-tert-butylphenol), 4,4′-butylidenebis (3-methyl-6-tert-butylphenol), triethylene glycol-N-bis- -(3-t-butyl-4-hydroxy-5-methylphenyl) propionate, 1,6-hexanediol bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, bis [2 -T-butyl-4-methyl-6- (3-t-butyl-5-methyl-2-hydroxybenzyl) phenyl] terephthalate, 3,9-bis [2- {3- (3-t-butyl-4 -Hydroxy-5-methylphenyl) propionyloxy} -1,1-dimethylethyl] -2,4,8,10-tetraoxaspiro [5,5] undecane, 4,4'-thiobis (6-t-butyl) -M-cresol), 4,4'-thiobis (3-methyl-6-tert-butylphenol), 2,2'-thiobis (4-methyl-6-tert-butylphenol), bis (3,5-di-) t- Til-4-hydroxybenzyl) sulfide, 4,4'-di and tri-thiobis (2,6-di-t-butylphenol), 2,2-thiodiethylenebis- [3 (3,5-di-t- Butyl-4-hydroxyphenyl) propionate], 2,4-bis (n-octylthio) -6- (4-hydroxy3 ′, 5′-di-t-butylanilino) -1,3,5-triazine, N, N′-hexamethylenebis- (3,5-di-tert-butyl-4-hydroxyhydrocinnamide, N, N′-bis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) Propionyl] hydrazine, calcium (3,5-di-tert-butyl-4-hydroxybenzyl monoethyl phosphonate), alkylated bisphenol, 1,1,3-tris (2-methyl-4-hydroxy) 5-t-butylphenyl) butane, 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene, tris (3,5-di-) t-butyl-4-hydroxyphenyl) isocyanurate, tris (3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate, 1,3,5-tris (4-t-butyl-3-hydroxy-) 2,6-dimethylbenzyl) isocyanurate, 1,3,5-tris 2 [3 (3,5-di-tert-butyl-4-hydroxyphenyl) propionyloxy] ethyl isocyanate, tetrakis [methylene-3- (3 ', 5'-di-tert-butyl-4-hydroxyphenyl) propionate] methane, butyric acid, 3,3-bis (3-tert-butyl-4-hydroxyphenyl) ethylene Steal, triphenyl phosphite, diphenylnonylphenyl phosphite, tris- (2,4-di-t-butylphenyl) phosphite, trisnonylphenyl phosphite, tris- (mono and di-mixed nonylphenyl) phosphite, diphenyl Isooctyl phosphite, 2,2′-methylenebis (4,6-di-t-butylphenyl) octyl phosphite, diphenylisodecyl phosphite, diphenyl mono (tridecyl) phosphite, 2,2′-ethylidene bis (4 , 6-di-t-butylphenol) fluorophosphite, phenyl diisodecyl phosphite, phenyl di (tridecyl) phosphite, tris (2-ethylhexyl) phosphite, tris (isodecyl) phosphite, tris (tridecyl) phosphat Ite, dibutyl hydrogen phosphite, trilauryl trithiophosphite, tetrakis (2,4-di-t-butylphenyl) 4,4'-biphenylene diphosphonite, 4,4'-isopropylidenediphenol alkyl (C12- C15) phosphite, 4,4′-butylidenebis (3-methyl-6-tert-butylphenyl) di-tridecyl phosphite, distearyl-pentaerythritol diphosphite, bis (nonylphenyl) pentaerythritol diphosphite, Bis (2,4-di-t-butylphenyl) pentaerythritol diphosphite, cyclic neopentanetetraylbis (2,6-di-t-butyl-4-methylphenyl phosphite, phenyl-bisphenol A pentaerythritol diphosphite Phosphite, Tetraf Nildipropylene glycol diphosphite, 1,1,3-tris (2-methyl-4-di-tridecylphosphite-5-t-butylphenyl) butane, tetraphenyltetra (tridecyl) pentaerythritol tetraphosphite, Zinc dialkyldithiophosphate (ZnDTP), 3,4,5,6-dibenzo-1,2-oxaphosphan-2-oxide, 3,5-di-tert-butyl-4-hydroxybenzyl phosphite-diethyl ester , Hydrogenated bisphenol A phosphite polymer, dilauryl-3,3′-thiodipropionic acid ester (DLTTDP), ditridecyl-3,3′-thiodipropionic acid ester, dimyristyl-3,3′-thiodipropionic acid ester (DMTDP), distearyl-3,3′-thiodipropi Acid ester (DSTDP), lauryl stearyl-3,3′-thiodipropionate, pentaerythritol tetra (β-lauryl-thiopropionate) ester, stearyl thiopropionamide, bis [2-methyl-4- ( 3-n-alkyl (C12-C14) thiopropionyloxy) -5-tert-butylphenyl] sulfide, dioctadecyl disulfide, 2-mercaptonbenzimidazole, 2-mercapto-6-methylbenzimidazole, 1,1′- Examples thereof include thiobis (2-naphthol).

Some light stabilizers are used as the above-mentioned antioxidants, but benzotriazole compounds, benzophenone compounds, salicylate compounds, cyanoacrylates, oxalic acid derivatives, hindered amine compounds (HALS), hindered phenols. Typified by series compounds. Suitable compounds include 2- (2′-hydroxy-5′-methylphenyl) benzotriazole, 3 ″, 4 ″, 2- (2′-hydroxy-5′-t-octylphenyl) benzotriazole, 2- (2′-hydroxy-4′-t-octoxyphenyl) benzotriazole, 2- (2′-hydroxy-3 ′, 5′-di-t-butylphenyl) benzotriazole, 2- (2′- Hydroxy-3 ′, 5′-di-t-amylphenyl) benzotriazole, 2- (2′-hydroxy-3′-dodecyl-5′-methylphenyl) benzotriazole, 2- (2′-hydroxy-3 ′) , 5′-bis (α, α-dimethylbenzyl) phenylbenzotriazole, 2- [2′-hydroxy-3 ′-(3 ″, 4 ″, 5 ″, 6 ″ -tetraphthalimidomethyl)- 5'-methylphenyl] benzotria 2- (2′-hydroxy-3′-t-butyl-5′-methylphenyl) -5-chlorobenzotriazole, 2- (2′-hydroxy-3 ′, 5′-di-t-butyl) Phenyl) -5-chlorobenzotriazole, 2,2'-methylenebis [4- (1,1,3,3-tetramethylbutyl) -6- (2H-benzotriazol-2-yl) phenol, methyl-3- [3-t-butyl-5- (2H-benzotriazol-2-yl) -4-hydroxyphenylpropionate-condensate with polyethylene glycol (molecular weight about 300), 2,4-dihydroxybenzophenone, 2-hydroxy- 4-methoxybenzophenone, 2-hydroxy-4-n-octoxybenzophenone, 2-hydroxy-4-n-dodecyloxybenzophenone, 2-hydroxy -4-benzyloxybenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-2'-carboxybenzophenone, 2-hydroxy-4-methoxy-5-sulfoxybenzophenone, 2,2 '-Dihydroxy-4,4'-dimethoxybenzophenone, 2,2', 4,4'-tetrahydroxybenzophenone, 2,2'-dihydroxy-4,4'-dimethoxy-5-sodiumsulfoxybenzophenone, bis ( 5-benzoyl-4-hydroxy-2-methoxyphenyl) methane, 4- (2-acryloyloxyethoxy) -2-hydroxybenzophenone polymer, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone and other Mixture with 4-substituted benzophenone, phenyl salicylate, 2,5-di t-butyl-4-hydroxybenzoic acid-n-hexadecyl ester, 4-t-butylphenyl salicylate, 4-t-octylphenyl salicylate, 2,4-di-t-butylphenyl-3 ′, 5′-di-t-butyl-4′-hydroxybenzoate, ethyl (β, β-diphenyl) cyanoacrylate, 2-ethylhexyl (β, β-diphenyl) cyanoacrylate, 2-ethoxy-2′-ethylsuccinic acid bisanilide, 2-ethoxy-5-t-butyl-2'-ethylsuccinic acid bisanilide, succinic acid anilide derivative, indole, azomethine, phenyl-4-piperidinyl carbonate, [4- (4-hydroxy-3,5-di- t-butylphenyl) propionyl] -N- (4-hydroxy-3,5-di-t-butylphenyl) methyl-2,2,6,6-te Tramethylpiperidine, 1,1 ′-(1,2-ethanediyl) bis (3,3,5,5-tetramethylpiperazinone), bis (2,2,6,6-tetramethyl-4-piperidinyl) sebacate Bis- [N-methyl-2,2,6,6-tetramethyl-piperidinyl sebacate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) -2- (3,5 -Di-t-butyl-4-hydroxybenzyl) -2-n-butylmalonate, 1,2,3,4-butanecarboxylic acid and 2,2,6,6-tetramethyl-4-piperidinol and tridecyl Condensate with alcohol, 1,2,3,4-butanecarboxylic acid, 1,2,2,6,6-pentamethyl-4-piperidinol and tridecyl alcohol, tetrakis (2,2,6, 6-tetramethyl-4 Piperidyl) -1,2,3,4-butanetetracarboxylate, tetrakis (1,2,2,6,6-pentamethyl-4-piperidyl) -1,2,3,4-butanetetracarboxylate, poly [ [6- (1,1,3,3-tetramethylbutylamino) -1,3,5-triazine-2,4-diyl] [(2,2,6,6-tetramethylpiperidine) imino] hexamethylene [(2,2,6,6-tetramethylpiperidyl) imino]], poly [6-morpholino-s-triazine-2,4-diyl-2,2,6,6-tetramethylpiperidylimino-hexamethylene] [2,2,6,6-tetramethylpiperidylimino]], 1,2,3,4-butanetetracarboxylic acid and 2,2,6,6-tetramethyl-4-piperidinol and β, β, β ′ , Β′-tetramethyl-3, -Condensate with (2,4,8,10-tetraoxaspiro [5,5] undecane) diethanol, 1,6-hexamethylenebis (N, N-dimethylsemicarbazide), 1,1,1 ', 1 Examples include '-tetramethyl-4,4'-(methylene-di-p-phenylene) disemicarbazide.
Examples of the polymerization inhibitor include phenols, quinones, nitro compounds, nitroso compounds, amines, and sulfides. Suitable compounds include hydroquinone, hydroquinone monomethyl ether, mono-tert-butylhydroquinone, catechol, p-tert-butylcatechol, p-methoxyphenol, p-tert-butylcatechol, 2,6-di-tert-butyl- phenols such as m-cresol, pyrogallol, β-naphthol, 4-methoxy-1-naphthol; quinones such as benzoquinone, 2,5-diphenyl-p-benzoquinone, p-toluquinone, p-xyloquinone; nitromethane, nitroethane, Nitrobutane, nitrobenzene, nitrobenzenesulfonic acid compound, m-dinitrobenzene, 2-methyl-2-nitrosopropane, α-phenyl-tert-butylnitrone, 5,5-dimethyl-1-pyrroline-1-oxide, and other nitro Compounds or nitroso compounds; amines such as chloranyl-amine, diphenylamine, diphenylpicrylhydrazine, phenol-α-naphthylamine, pyridine, phenothiazine; sulfides such as dithiobenzoyl sulfide and dibenzyltetrasulfide.

  Examples of the surfactant used in the present invention include polyoxyalkylene alkyl ethers such as polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether; polyoxyethylene octyl phenyl ether, Polyoxyalkylene alkyl phenyl ethers such as polyoxyethylene nonylphenyl ether; polyoxyalkylene alkyl amino ethers such as polyoxyethylene lauryl amino ether and polyoxyethylene stearyl amino ether; sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostea Sorbitan fatty acid esters such as rate and sorbitan monooleate; polyoxyethylene sorbitan monora Polyoxyalkylene sorbitan fatty acid esters such as polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan monooleate, polyethylene glycol monolaurate, polyethylene glycol monooleate, polyethylene glycol monostearate Polyalkylene glycol fatty acid esters such as acrylate, polyethylene glycol dilaurate, polyethylene glycol distearate; nonionic surfactants typified by glycerin fatty acid esters such as lauric acid monoglyceride, stearic acid monoglyceride, oleic acid monoglyceride, etc. Sodium oxyethylene lauryl ether sulfate, polyoxyethylene octylsulfate Sulfate esters such as sodium nyl ether sulfate, polyoxyethylene nonyl phenyl ether sodium sulfate, triethanolamine lauryl sulfate, sodium lauryl sulfate, potassium lauryl sulfate, ammonium lauryl sulfate; sodium dodecylbenzenesulfonate, sodium alkylnaphthalenesulfonate, dialkylsulfosuccinic acid Sulfonic acid salts such as sodium; anionic surfactants typified by phosphate ester salts such as potassium alkyl phosphate, lauryltrimethylammonium chloride, stearyltrimethylammonium chloride, cetyltrimethylammonium chloride, stearyltrimethylammonium chloride Cationic surfactants typified by quaternary ammonium salts such as 1 type or 2 types or more selected from these can be used. Among these, particularly preferred examples include polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether or a mixture thereof.

  The heteropolyanion compound or mixed coordination type heteropolyanion compound used in the present invention may be added when the raw metal powder is pulverized by a ball mill, or may be mixed in a slurry state in which a solvent is added to a metal pigment. Then, the paste may be kneaded in a paste state in which the amount of the solvent is reduced. Moreover, the heteropolyanion compound or the mixed coordination type heteropolyanion compound may be added to the metal pigment as it is, or may be diluted with a solvent. In order to obtain a uniform mixed state, it is preferable to dilute with a solvent in advance. Examples of the solvent used for dilution include water, alcohols such as methanol and isopropanol, cellosolves such as propylene glycol monomethyl ether, hydrocarbon solvents such as hexane, octane, isooctane, benzene, toluene, xylene, tetralin and decalin, Examples include industrial gasoline such as mineral spirits and solvent naphtha, esters such as ethyl acetate and butyl acetate, ketones such as methyl ethyl ketone, methyl isobutyl ketone and cyclohexane, and mineral oil.

  The inorganic phosphoric acid or salts thereof used in the present invention may be added when the raw metal powder is pulverized with a ball mill, may be mixed in a slurry state in which a solvent is added to a metal pigment, or the amount of the solvent You may knead | mix in the paste state which decreased less. These may be added after treating the metal pigment with the heteropolyanion compound or mixed coordination type heteropolyanion compound, or may be added simultaneously with the heteropolyanion compound or mixed coordination type heteropolyanion compound. Or it is more preferable to add after processing with a mixed coordination type heteropolyanion compound. In order to obtain a uniform mixed state, it is preferable to dilute with a solvent in advance. Solvents used for dilution include, for example, alcohols such as water, methanol and isopropanol, cellosolves such as propylene glycol monomethyl ether, hydrocarbon solvents such as hexane, octane, isooctane, benzene, toluene, xylene, tetralin and decalin, minerals Examples include industrial gasoline such as spirit and solvent naphtha, esters such as ethyl acetate and butyl acetate, ketones such as methyl ethyl ketone, methyl isobutyl ketone and cyclohexane, and mineral oil.

  The antioxidant, light stabilizer, and polymerization inhibitor used in the present invention may be added when the raw metal powder is pulverized by a ball mill, or may be mixed in a slurry state in which a solvent is added to a metal pigment. Alternatively, the paste may be kneaded in a paste state with a small amount of solvent. These may be added after treating the metal pigment with the heteropolyanion compound or mixed coordination type heteropolyanion compound, or may be added simultaneously with the heteropolyanion compound or mixed coordination type heteropolyanion compound. Or it is more preferable to add after processing with a mixed coordination type heteropolyanion compound. In addition, the metal pigment composition may be added to a water-based paint or water-based ink in which a resin as a coating film-forming component is dissolved or dispersed in a water-based medium. In order to obtain a uniform mixed state, it is preferable to dilute with a solvent in advance. Solvents used for dilution include, for example, alcohols such as water, methanol and isopropanol; cellosolves such as propylene glycol monomethyl ether; hydrocarbon solvents such as hexane, octane, isooctane, benzene, toluene, xylene, tetralin and decalin; minerals Examples include industrial gasoline such as spirit and solvent naphtha, esters such as ethyl acetate and butyl acetate; ketones such as methyl ethyl ketone, methyl isobutyl ketone and cyclohexane; mineral oil and the like.

  The surfactant used in the present invention may be added when the raw metal powder is pulverized by a ball mill, may be mixed in a slurry state in which a solvent is added to a metal pigment, or the amount of the solvent is reduced. You may knead | mix in a paste state. These may be added after treating the metal pigment with the heteropolyanion compound or mixed coordination type heteropolyanion compound, or may be added simultaneously with the heteropolyanion compound or mixed coordination type heteropolyanion compound. Or it is more preferable to add after processing with a mixed coordination type heteropolyanion compound. In addition, the metal pigment composition may be added to a water-based paint or water-based ink in which a resin as a coating film-forming component is dissolved or dispersed in a water-based medium. In order to obtain a uniform mixed state, it is preferable to dilute with a solvent in advance. Solvents used for dilution include, for example, alcohols such as water, methanol and isopropanol; cellosolves such as propylene glycol monomethyl ether; hydrocarbon solvents such as hexane, octane, isooctane, benzene, toluene, xylene, tetralin and decalin, minerals Industrial gasoline such as spirit and solvent naphtha; esters such as ethyl acetate and butyl acetate; ketones such as methyl ethyl ketone, methyl isobutyl ketone and cyclohexane; mineral oil and the like.

  The solvent used in preparing the metal pigment composition of the present invention may be a hydrophilic solvent or a hydrophobic solvent. Examples of the hydrophilic solvent include alcohols such as methanol, ethanol, propanol, butanol, isopropanol, and octanol; ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, propylene glycol monoethyl ether, propylene Cellosolves such as glycol monomethyl ether and dipropylene glycol monomethyl ether; and esters thereof, propylene glycol, polyoxyethylene glycol, polyoxypropylene glycol, ethylene propylene glycol and the like. Examples of the hydrophobic solvent include mineral spirit, solvent naphtha, LAWS (Low Aromatic White Spirit), HAWS (High Aromatic White Spirit), toluene, xylene, and the like. Furthermore, esters such as ethyl acetate and butyl acetate, and ketones such as methyl ethyl ketone, methyl isobutyl ketone and cyclohexane can also be used. These can be used alone or in combination.

When prepared in a slurry state, the concentration of the metal pigment in the slurry is 1 to 50% by weight, preferably 10 to 30% by weight. When kneaded in the paste state, the concentration of the metal pigment is 50 to 95% by weight. %, Preferably 60 to 85% by weight.
The heteropolyanion compound or mixed coordination type heteropolyanion compound is added in an amount of 0.01 to 10 parts by weight, preferably 0.01 to 5 parts by weight, per 100 parts by weight of the metal component in the metal pigment. These are preferably added after being dissolved or dispersed in a solvent in advance.

  Inorganic phosphoric acid or a salt thereof is added in an amount of 0.01 to 10 parts by weight, preferably 0.01 to 5 parts by weight, per 100 parts by weight of the metal component in the metal pigment. These are preferably added after being dissolved or dispersed in a solvent in advance.

  The antioxidant, light stabilizer, and polymerization inhibitor are added in an amount of 0.01 to 10 parts by weight, preferably 0.01 to 5 parts by weight, based on 100 parts by weight of the metal component in the metal pigment. These are preferably added after being dissolved or dispersed in a solvent in advance.

  The surfactant is added in an amount of 0.01 to 30 parts by weight, preferably 0.01 to 20 parts by weight, per 100 parts by weight of the metal component in the metal pigment. These are preferably added after being dissolved or dispersed in a solvent in advance.

  The order of adding these is not particularly limited, but at the same time or after the metal pigment is treated with the heteropolyanion compound or the mixed coordination type heteropolyanion compound, inorganic phosphoric acid or a salt thereof is added, and finally an antioxidant, It is preferable to add a light stabilizer, a polymerization inhibitor, and a surfactant. An antioxidant, a light stabilizer, and a polymerization inhibitor and a surfactant, a water-based paint in which a resin that is a film-forming component is dissolved or dispersed in a water-based medium, a metal pigment composition, You may add when mix | blending with water-based ink.

  This mixture is stirred and mixed at a temperature of 10 to 160 ° C., preferably 20 to 120 ° C. for 10 minutes to 72 hours, preferably 20 minutes to 48 hours. If the solvent is high, remove it to bring the final metal pigment content to the desired 40-90%. The resulting metal pigment composition may be aged at 40 ° C. to 120 ° C., preferably 50 ° C. to 110 ° C. for 6 hours to 3 months, preferably 1 day to 30 days.

  The metallic pigment composition obtained by the present invention is added to an aqueous paint or aqueous ink in which a resin that is a film-forming component is dissolved or dispersed in a medium mainly containing water, thereby forming a metallic aqueous paint or metallic aqueous paint. Ink can be used. The metal pigment composition may be added to the water-based paint or water-based ink as it is, but it is preferable to add the metal pigment composition after previously dispersing it in a solvent. Examples of the solvent to be used include water, texanol, diethylene glycol monobutyl ether, propylene glycol monomethyl ether and the like. Examples of these resins include acrylic resins, polyester resins, polyether resins, epoxy resins, fluororesins, and rosin resins.

As acrylic resins, for example, methyl (meth) acrylate, ethyl (meth) acrylate, isopropyl (meth) acrylate, (n-butyl) (meth) acrylate, 2-ethylhexyl (meth) acrylate, ( (Meth) acrylic acid esters such as methacrylic acid lauryl; (meth) acrylic acid-2-hydroxyethyl, (meth) acrylic acid-2-hydroxypropyl, (meth) acrylic acid-2-hydroxybutyl, ) (Meth) acrylic acid esters having active hydrogen such as acrylic acid-3-hydroxypropyl and (meth) acrylic acid-4-hydroxybutyl; unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic acid and itaconic acid Unsaturated amides such as acrylamide, N-methylol acrylamide, diacetone acrylamide, and glycidyl methacrylate, Acrylic resins obtained by polymerizing a single or a mixture selected from other polymerizable monomers such as tylene, vinyl toluene, vinyl acetate, acrylonitrile, dibutyl fumarate, p-styrene sulfonic acid, and allyl sulfosuccinic acid. It is done.
The polymerization method is generally emulsion polymerization, but can also be produced by suspension polymerization, dispersion polymerization, or solution polymerization. In emulsion polymerization, it can also be polymerized stepwise.

  The polyester resins were selected from the group of carboxylic acids such as succinic acid, adipic acid, sebacic acid, dimer acid, maleic anhydride, phthalic anhydride, isophthalic acid, terephthalic acid, trimellitic acid, pyromellitic acid, etc. For example, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, 1,2-propanediol, 1,3-propanediol, , 2-butanediol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 2-methyl-1,2-propanediol, 1,5-pentanediol, 2-methyl-2 , 3-Butanediol, 1,6-hexane All, 1,2-hexanediol, 2,5-hexanediol, 2-methyl-2,4-pentanediol, 2,3-dimethyl-2,3-butanediol, 2-ethyl-hexanediol, 1,2 -Octanediol, 1,2-decanediol, 2,2,4-trimethylpentanediol, 2-butyl-2-ethyl-1,3-propanediol, 2,2-diethyl-1,3-propanediol, etc. Examples of the triols include glycerin and trimethylolpropane, and examples of the tetraols include condensation of a polyhydric alcohol selected from the group of diglycerin, dimethylolpropane, pentaerythritol and the like alone or in a mixture. Polyester resins obtained by the reaction and e.g. And polycaprolactones obtained by ring-opening polymerization of prolactone.

  Polyether resins include, for example, polyhydric hydroxy compounds, alone or in mixture, using a strong basic catalyst such as hydroxides such as lithium, sodium and potassium, alcoholates and alkylamines, ethylene oxide, propylene oxide, Polyether polyols obtained by adding a single or mixture of alkylene oxides such as butylene oxide, cyclohexene oxide and styrene oxide, polyether polyols obtained by reacting alkylene oxide with a polyfunctional compound such as ethylenediamine, and So-called polymer polyols obtained by polymerizing acrylamide or the like using these polyethers as a medium are included.

  These resins are preferably emulsified, dispersed or dissolved in water. Therefore, the carboxyl group, the sulfone group, etc. contained in the resins can be neutralized.

  Examples of neutralizing agents for neutralizing carboxyl groups and sulfone groups include ammonia and water-soluble amino compounds such as monoethanolamine, ethylamine, dimethylamine, diethylamine, triethylamine, propylamine, dipropylamine, and isopropylamine. , Diisopropylamine, triethanolamine, butylamine, dibutylamine, 2-ethylhexylamine, ethylenediamine, propylenediamine, methylethanolamine, dimethylethanolamine, diethylethanolamine, morpholine and the like can be used. Preferably, tertiary amines such as triethylamine and dimethylethanolamine are used.

Preferred resins are acrylic resins and polyester resins.
If necessary, a resin such as a melamine curing agent, an isocyanate curing agent, or a urethane dispersion can be used in combination. Furthermore, in combination with inorganic pigments, organic pigments, extender pigments, silane coupling agents, titanium coupling agents, dispersants, anti-settling agents, leveling agents, thickeners and antifoaming agents that are generally added to paints. Also good. In order to improve the dispersibility in the paint, a surfactant may be further added, and in order to improve the storage stability of the paint, an antioxidant, a light stabilizer, and a polymerization inhibitor are further added. May be.

Examples of the present invention are shown below.
[Example 1]
While stirring a slurry in which 465 g of propylene glycol monomethyl ether was added to 135 g of a commercially available aluminum paste (trade name “GX-3100 (average particle size 10.5 μm, nonvolatile content 74%)” manufactured by Asahi Kasei Chemicals Corporation), A solution of 0.2 g of phosphomolybdic acid (H ₃ PMo ₁₂ O ₄₀ ) hydrate dissolved in 30 g of water was gradually added, and the mixture was stirred for 2 hours while maintaining the slurry temperature at 70 ° C. Thereafter, a solution obtained by dissolving 0.5 g of an 85% aqueous phosphoric acid solution in 30 g of water was gradually added and stirred for 4 hours. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 69%.

[Example 2]
While stirring a slurry in which 465 g of ethylene glycol monobutyl ether was added to 135 g of a commercially available aluminum paste (trade name “GX-3100 (average particle size 10.5 μm, nonvolatile content 74%)” manufactured by Asahi Kasei Chemicals Corporation), A solution prepared by dissolving 0.5 g of hydrated phosphovanadmolybdic acid (H ₄ PV ₁ Mo ₁₁ O ₄₀ ) in 30 g of ethylene glycol monobutyl ether was gradually added, and the mixture was stirred for 2 hours while maintaining the slurry temperature at 40 ° C. Thereafter, a solution obtained by dissolving 1.0 g of 85% phosphoric acid aqueous solution in 30 g of ethylene glycol monobutyl ether was gradually added and stirred for 2 hours. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 70%. Further, 0.5 parts by weight of 2,6-di-t-butyl-p-cresol was added to and kneaded with 100 parts by weight of the aluminum metal component of the aluminum pigment composition. The obtained aluminum pigment composition was aged at 50 ° C. for 1 week.

[Example 3]
While stirring a slurry in which 465 g of ethylene glycol monobutyl ether was added to 135 g of a commercially available aluminum paste (trade name “GX-3100 (average particle size 10.5 μm, nonvolatile content 74%)” manufactured by Asahi Kasei Chemicals Corporation), A solution prepared by dissolving 0.5 g of phosphotungstomolybdic acid (H ₃ PW ₃ Mo ₉ O ₄₀ ) in 30 g of isopropanol was gradually added, and the mixture was stirred for 2 hours while maintaining the slurry temperature at 70 ° C. Thereafter, a solution obtained by dissolving 2.0 g of polyphosphoric acid (105% in terms of phosphoric acid) in 30 g of isopropanol was gradually added and stirred for 2 hours. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 68%.

[Example 4]
While stirring a slurry in which 465 g of propylene glycol monomethyl ether was added to 135 g of a commercially available aluminum paste (trade name “GX-3100 (average particle size 10.5 μm, nonvolatile content 74%)” manufactured by Asahi Kasei Chemicals Corporation), A solution of 1.0 g of silicomolybdic acid (H ₄ SiMo ₁₂ O ₄₀ ) hydrate dissolved in 30 g of propylene glycol monomethyl ether was gradually added, and the mixture was stirred for 2 hours while maintaining the slurry temperature at 40 ° C. Thereafter, a solution prepared by dissolving 2.5 g of triethanolamine phosphate in 30 g of propylene glycol monomethyl ether was gradually added and stirred for 2 hours. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 69%.

[Production Example 1]
135 g of commercially available aluminum paste (trade name “GX-3100 (average particle size: 10.5 μm, non-volatile content: 74%)” manufactured by Asahi Kasei Chemicals Co., Ltd.) is added with phosphotungstic acid monooctylamine salt and oleic acid. It added so that it might become 0.3 weight part and 0.5 weight part with respect to 100 weight part of aluminum metal components, respectively, and it stirred at 70 degreeC for 6 hours.

[Production Example 2]
To 135 g of commercially available aluminum paste (trade name “GX-3100 (average particle size 10.5 μm, non-volatile content 74%)” manufactured by Asahi Kasei Chemicals Corporation), lintongue molybdate (H ₃ PW ₆ Mo ₆ O ₄₀ ) ditri Decylamine salt and 2,6-di-t-butyl-p-cresol were added in an amount of 0.5 parts by weight with respect to 100 parts by weight of the aluminum metal component in the aluminum paste. Stir for 6 hours.

[Example 5]
465 g of ethylene glycol monobutyl ether was added to 135 g of the aluminum pigment composition obtained in Production Example 1 to form a slurry, and 2.0 parts by weight of monohydrogen phosphate with respect to 100 parts by weight of the aluminum metal component in the aluminum pigment composition. Diammonium was added and stirred at 70 ° C. for 4 hours. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 70%.

[Example 6]
465 g of propylene glycol monomethyl ether was added to 135 g of the aluminum pigment composition obtained in Production Example 2 to form a slurry, and 1.0 part by weight of phosphoric acid was added to 100 parts by weight of the aluminum metal component in the aluminum pigment composition. And stirred at 70 ° C. for 4 hours. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 73%.

[Comparative Example 1]
While stirring a slurry in which 465 g of propylene glycol monomethyl ether was added to 135 g of a commercially available aluminum paste (trade name “GX-3100 (average particle size 10.5 μm, nonvolatile content 74%)” manufactured by Asahi Kasei Chemicals Corporation), A solution of 0.2 g of phosphomolybdic acid (H ₃ PMo ₁₂ O ₄₀ ) hydrate dissolved in 30 g of propylene glycol monomethyl ether was gradually added, and the mixture was stirred for 2 hours while maintaining the slurry temperature at 70 ° C. Thereafter, filtration was performed to obtain an aluminum pigment composition having a nonvolatile content of 75%.

[Examples 7 to 12, Comparative Example 2]
For the aluminum pigment compositions obtained in Examples 1 to 6 and Comparative Example 1, water-based metallic paints were prepared with the following compositions.

[Adjustment of water-based metallic paint]
Aluminum pigment composition: 10.5 g as aluminum content
Diethylene glycol monobutyl ether: 6.8 g
Polyoxyethylene lauryl ether (nonionic surfactant)
(Matsumoto Yushi Seiyaku Co., Ltd., trade name “Actinol L5”): 2.1 g
Purified water: 42g
Water-soluble acrylic resin (manufactured by Origin Electric Co., Ltd., trade name “Aqueous Plamise # 300”): 175 g
Thickener (Kyoeisha Chemical Co., Ltd., trade name “Tikuzol K-130B”): 5.0 g
The following evaluation was performed using the produced water-based metallic paint.

[Evaluation 1 (Storage stability evaluation)]
200 g of the aqueous metallic paint was collected in a flask and the amount of hydrogen gas accumulated was observed in a constant temperature water bath at 40 ° C. for 240 hours. It was evaluated as follows according to the amount of gas generated and used as an index of storage stability in the paint.
○: Less than 1.0 ml Δ: 1.0 or more and less than 5.0 ml ×: 5.0 ml or more

[Evaluation 2 (Evaluation of color tone of coating film)]
A coating film was prepared using the above-mentioned paint, and the brightness, flip-flop feeling, hiding property, and particle feeling were evaluated.
The brightness was evaluated using a laser-type metallic feeling measuring apparatus Alcorp LMR-200 manufactured by Kansai Paint Co., Ltd. The optical conditions include a laser light source with an incident angle of 45 degrees and a light receiver with light receiving angles of 0 degrees and -35 degrees. As a measured value, IV value was calculated | required by the light reception angle -35 degree which can obtain the maximum light intensity except the light of the specular reflection area | region reflected on the coating-film surface among the reflected light of a laser. The IV value is a parameter proportional to the intensity of specularly reflected light from the coating film and represents the magnitude of light luminance. The determination method is as follows.
◎: 10 or more higher than Comparative Example 2 ○: Difference from Comparative Example 2 is less than 10 ×: 10 or more lower than Comparative Example 2 Flip-flop feeling is a color change colorimeter manufactured by Suga Test Instruments Co., Ltd. Was used to evaluate. The F / F value was determined from the logarithmic slope of the reflected light intensity (L value) at an observation angle (light receiving angle) of 30 degrees and 80 degrees with respect to a light source having an incident angle of 45 degrees. The F / F value is a parameter proportional to the degree of orientation of the metal pigment, and represents the magnitude of the flip-flop feeling of the pigment. The determination method is as follows.
A: 0.05 or more higher than Comparative Example 2 ○: Difference from Comparative Example 2 is less than 0.05 ×: Lower 0.05 or more than Comparative Example 2 The concealing property was visually observed. The determination method is as follows.
○: Better than Comparative Example 2 ×: Inferior to Comparative Example 2 Table 1 shows the results of Evaluations 1 and 2.

  The present invention can be used in paint compositions or ink compositions, particularly water-based paints or water-based ink-based water paints, and is excellent in storage stability of paints. Thus, it is possible to provide a metal pigment composition with less decrease in the above.

Claims (19)

A metal pigment composition comprising at least one heteropolyanion compound or a mixed coordination heteropolyanion compound, inorganic phosphoric acid or a salt thereof, and a metal pigment , wherein the heteropolyanion constituting the heteropolyanion compound is [ ^{_{X a + M b + 12 O}} 2- 40] (80-a-12b) - is represented by the mixing coordinated heteropoly anion constituting the mixed coordinated heteropolyanion compounds ^{_{[X a + M b + x}} N c + 12- ^{_{x O 2- 40] {80-}} a-bx-c (12-x)} - a metal pigment composition represented by (wherein, X represents B, Si, Ge, P, and as, M, N is Ti, Zr, V, Nb, Ta, Mo, W are represented) .   The metal pigment composition according to claim 1, wherein the metal pigment is aluminum flakes. Heteropolyanion compounds are H ₃ PMo ₁₂ O ₄₀ · nH ₂ O (phosphomolybdic acid · n hydrate), H ₃ PW ₁₂ O ₄₀ · nH ₂ O (phosphotungstic acid · n hydrate), H ₄ SiMo is at least one selected from the ₁₂ O ₄₀ · _nH 2 O (silicomolybdic acid · n-hydrate) and _{H 4 SiW 12 O 40 · nH} 2 O the group consisting of (silicotungstic acid · n hydrate), The metal pigment composition according to claim 1 or 2. Mixing coordinated heteropolyanion _{compounds, H 3 PW x Mo 12-} x O 40 · nH 2 O ( phosphorus (tungsto) molybdic acid · _{n-hydrate), H 3 + x PV x} Mo 12-x O 40 · nH 2 O (phosphorus (vanado) molybdic acid · n hydrate), H ₄ SiW _x Mo _12-x O ₄₀ · nH ₂ O (silk (tungsto) molybdic acid · n hydrate) and H _{4 + x} SiV _x Mo _12- is at least one selected from the _x O ₄₀ · _nH 2 O the group consisting of (Kay (Banado) molybdate · n-hydrate), metal pigment composition according to claim 1 or 2. (However, 1 ≦ x ≦ 11, n ≧ 0) Heteropolyanion compounds, and heteropoly anion constituting the heteropolyanion compounds, alkali metal, salts of alkaline earth metals, and one selected from the group consisting of ammonia, according to any one of claims 1 3 Metal pigment composition. The mixed coordination heteropolyanion compound is a salt of a mixed coordination heteropolyanion constituting the mixed coordination heteropolyanion compound and one selected from the group consisting of alkali metals, alkaline earth metals, and ammonia. The metal pigment composition according to any one of claims 1 to 4 . Heteropolyanion compounds, and heteropoly anion constituting the heteropoly anion compound, a salt of at least one selected from amine compounds represented by the following general formula (1), according to any one of claims 1 3 Metal pigment composition.

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.) Mixing coordinated heteropolyanion compounds, and mixtures coordinated heteropoly anion constituting the mixed coordinated heteropolyanion compounds, salts with at least one selected from amine compounds represented by the following general formula (2) wherein Item 5. The metal pigment composition according to any one of Items 1 to 4 .

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.)   The metal pigment composition according to claim 1 or 2, wherein the inorganic phosphoric acid is at least one selected from orthophosphoric acid, metaphosphoric acid, pyrophosphoric acid, triphosphoric acid, tetraphosphoric acid, and phosphorous acid. The metal pigment composition according to claim 1 or 2, wherein the inorganic phosphate is a salt of inorganic phosphoric acid, an alkali metal, an alkaline earth metal, ammonia, or an amine represented by the following general formula (3).

(In the formula, R 1, R 2 and R 3 may be the same or different, and may be a hydrogen atom or a monovalent group having 1 to 30 carbon atoms and optionally containing an ether bond, an ester bond, a hydroxyl group, a carbonyl group, or a thiol group. Or a divalent hydrocarbon group, optionally R1 and R2 taken together to form a 5- or 6-membered cycloalkyl group, or optionally R1 and R2 taken together with a nitrogen atom to form a bridge Forms a 5- or 6-membered ring which may additionally contain nitrogen or oxygen atoms as members, or optionally R1, R2 and R3 together form one or more additional nitrogen atoms and / or Or a multi-membered multi-ring composition that can contain an oxygen atom as a bridging member, R1, R2, and R3 cannot simultaneously be hydrogen atoms, n represents a number from 1 to 2.) The metal pigment composition according to claim 9 , wherein the inorganic phosphoric acid is at least one selected from the group consisting of orthophosphoric acid, metaphosphoric acid, and pyrophosphoric acid. The inorganic phosphate part of the inorganic phosphate is at least one selected from orthophosphoric acid, metaphosphoric acid, and pyrophosphoric acid, and the basic part that forms the salt is ammonia, morpholine, represented by the following general formulas (4) and (5) The metal pigment composition according to claim 10 , wherein the metal pigment composition is at least one selected from ethanolamines represented by alkylamines represented by the following general formula (6):

(In the formula, at least one of R 4, R 5 and R 6 is the following general formula (5), and the other represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms.)

(In the formula, at least one of R7, R8, and R9 is a hydrocarbon group having 6 to 20 carbon atoms, and the other represents a hydrogen atom or a hydrocarbon group having 1 to 5 carbon atoms.) The metal pigment composition according to any one of claims 1 to 8, wherein the heteropolyanion compound or the mixed coordination type heteropolyanion compound is present in an amount of 0.01 to 10 parts by weight with respect to 100 parts by weight of the metal pigment. The metal pigment composition according to any one of claims 1 to 12, wherein the inorganic phosphoric acid or a salt thereof is present in an amount of 0.01 to 10 parts by weight with respect to 100 parts by weight of the metal pigment. Further antioxidants, light stabilizers, and with respect to 100 parts by weight of the metal pigment at least one selected from polymerization inhibitors, according to claim 1 containing 5 parts by weight 0.01 14 Metal pigment composition The metal pigment composition according to any one of claims 1 to 15, further comprising 0.01 to 30 parts by weight of a surfactant relative to 100 parts by weight of the metal pigment. The metal pigment, in a solvent optionally containing water, a heteropolyanion compounds or mixtures coordinated heteropolyanion compounds, the inorganic phosphoric acid or its salts, mixed treated in a separate step or the same step, the claims 1-14 The manufacturing method of the metal pigment composition in any one of. The coating composition containing the metal pigment composition in any one of Claims 1-16 . An ink composition comprising the metal pigment composition according to claim 1 .