JPH06256574A - Copolymer latex for water-based maskant - Google Patents

Abstract

PURPOSE:To obtain a copolymer latex, comprising a latex prepared by carrying out the emulsion copolymerization of a conjugated diene with an aromatic vinyl compound, an unsaturated carboxylic acid and a comonomer and another latex having a specific glass transition temperature and excellent in dimensional accuracy, coating properties, etc., without causing air pollution. CONSTITUTION:This copolymer latex is obtained by blending a copolymer latex prepared by carrying out the emulsion copolymerization of a monomer mixture composed of (A) 30-70wt.% aliphatic conjugated diene compound (e.g. 1,3-butadiene), (B) 20-70wt.% aromatic vinyl compound (e.g. styrene), (C) 0-10wt.% ethylenically unsaturated carboxylic acid (e.g. acrylic acid) and (D) 0-50wt.% other copolymerizable monomers (e.g. n-butyl acrylate) in an amount of 5-95wt.% (expressed in terms of solid content) with (E) another (co)polymer latex having -50 to +50 deg.C glass transition temperature measured by the scanning differential calorimetric method in an amount of 95-5wt.% (expressed in terms of the solid content). This latex is good in dimensional accuracy of a maskant in etching, coating properties of a masking agent and removing operation efficiency of the maskant.

Description

Detailed Description of the Invention

[0001]

INDUSTRIAL APPLICABILITY The present invention has excellent properties such as chemical resistance and heat resistance required as a masking agent in etching, and has excellent coating properties and workability for removing a maskant, and does not generate harmful gas. The present invention relates to a copolymer latex for an aqueous maskant, which is excellent in environmental hygiene and is preferably used in the metal chemical milling method.

[0002]

2. Description of the Related Art Metal chemical milling for removing unnecessary portions of metal products by etching with a strong acid or a strong base is well known. Especially in the aviation industry, it is required to reduce the weight of aircraft parts, and this means is used.

This metal chemical milling is usually performed by the following procedure. (A) A maskant that can withstand the etching bath used is formed on the metal substrate by means such as dipping. (B) The applied maskant is carved using a suitable template (template), and a predetermined portion of the maskant is peeled off to expose a metal portion to be selectively etched. (C) Next, the exposed metal portion is removed by etching using an etchant, for example, an alkaline solution for aluminum parts and an acid solution for titanium parts.

By the way, conventionally, as a masking agent used in the metal chemical milling method, a rubber solution in which rubber is dissolved in an organic solvent (for example, toluene / xylene or perchloroethylene) is used. Therefore, the organic solvent evaporates in the process of applying and drying the masking agent, and as a result, odors and air pollution are serious problems in environmental hygiene.

Therefore, recently, instead of the above rubber solution,
A method of using an aqueous rubber latex that does not use an organic solvent has been studied. However, the use of an alkaline etching agent, which is the mainstream of etching agents, causes the following problems. The peripheral part of the mascant easily swells with alkaline liquid, and chemical milling with high dimensional accuracy cannot be performed. The coating workability is poor because the coating property of the masking agent is not good. Since the maskant has poor peelability, the workability of removing the maskant is poor.

The present inventors have found that the use of a conjugated diene-aromatic vinyl copolymer latex as the aqueous rubber latex improves the above-mentioned drawbacks.
Further, a technique has already been proposed for improving the workability of removing the maskant and the strength of the maskant by using natural rubber in combination (see Japanese Patent Application No. 4-279347).

[0007]

The present invention has been made against the background of the above-mentioned problems of the prior art, and its object is to obtain film strength, chemical resistance, heat resistance and maskant required as a masking agent in etching. An object of the present invention is to provide a water-based copolymer latex for a maskant which is excellent in various properties such as dimensional accuracy, coatability of a masking agent and workability of removing a maskant, and which has no environmental health problems such as air pollution.

[0008]

[Means for Solving the Problems] The objects are: (a) 30 to 70% by weight of an aliphatic conjugated diene compound, (b) 20 to 70% by weight of an aromatic vinyl compound, and (c) an ethylenically unsaturated carboxylic acid. 10 to 10% by weight, (d) 0 to 50% by weight of another copolymerizable monomer, 5 to 95% by weight (in terms of solid content) of a copolymer latex obtained by emulsion polymerization of a monomer consisting of , (Co) polymer latex having a glass transition temperature of −50 to 50 ° C. by differential scanning calorimetry 95 to 5% by weight (solid content conversion)
It is achieved by a copolymer latex for an aqueous maskant, which comprises:

Further, the above objects are (e) 30 to 100% by weight of unsaturated acrylic acid ester, (f) 0 to 10% by weight of ethylenically unsaturated carboxylic acid, and (g) another copolymerizable monomer. (Co) polymer latex obtained by emulsion polymerization of a monomer consisting of 0 to 70% by weight (solid content) and a glass transition temperature of -50 to 50 by differential scanning calorimetry. ℃
The copolymer latex for an aqueous maskant is characterized by containing 95 to 0% by weight (in terms of solid content) of the (co) polymer latex. (Structure of the Invention) The present invention will be described in detail below.

First, it is used for producing a copolymer latex (hereinafter referred to as "copolymer latex (A-1)") comprising the monomer components (a) to (d) of claim 1 of the present invention. The monomer component used will be described. Examples of the aliphatic conjugated diene compound as the component (a) include 1,3
-Butadiene, 2-methyl-1,3-butadiene, 2,
Examples thereof include 3-dimethyl-1,3-butadiene, 2-neopentyl-1,3-butadiene, 2-chloro-1,3-butadiene, 2-cyano-1,3-butadiene and the like. Of these, the use of 1,3-butadiene is preferred. These (a) components may be used alone or
Further, two or more kinds can be used in combination.

The proportion of component (a) used is 30 to 70% by weight, preferably 35 to 65% by weight, and more preferably 40 to 60% by weight, based on the total monomers. When the amount of the component (a) used is less than 30% by weight, the coatability is poor, and the coating film is too hard and the releasability is poor, and the workability of removing the maskant is poor. On the other hand, when the amount of the component (a) used exceeds 70% by weight, the coatability is poor, and the coating becomes too soft to be stretched when peeled off, resulting in poor workability for removing the maskant.

Examples of the aromatic vinyl compound as the component (b) include styrene, α-methylstyrene, p-methylstyrene, vinyltoluene and chlorostyrene, and styrene is particularly preferable. These (b) components are
One kind may be used alone, or two or more kinds may be used in combination.

The proportion of the component (b) used is 20 to 70% by weight, preferably 25 to 65% by weight, and more preferably 30 to 60% by weight, based on all the monomers. When the amount of the component (b) used is less than 20% by weight, the coatability is poor, and the coating film becomes too soft and stretches when peeled off, resulting in poor workability for removing the maskant. On the other hand, (b)
If the amount of the component used exceeds 70% by weight, the coatability will be poor,
Furthermore, the coating film becomes too hard and the peelability is poor, and the workability of removing the maskant is poor.

Examples of the ethylenically unsaturated carboxylic acid as the component (c) include itaconic acid, acrylic acid, methacrylic acid, fumaric acid, maleic acid, maleic anhydride, fumaric anhydride and the like. The preferred component (c) is acrylic acid and methacrylic acid, which may be used alone or in combination of both. These components (c) may be neutralized with an alkali metal such as sodium or potassium, and may be used alone or in combination of two or more.
The amount of component (c) used is 0 to 10% by weight, preferably 0 to 8% by weight, more preferably 0.1
~ 8% by weight. The component (c) is mainly used for obtaining good polymerization stability, but serves to further improve the dimensional accuracy of the maskant. However, when the amount of the component (c) used exceeds 10% by weight, the water resistance of the coating film is lowered, so that it is not possible to obtain a maskant having excellent alkali resistance, resulting in lack of practicality.

Other copolymerizable monomers of component (d) include, for example, methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate and the like. (Meth) acrylic acid alkyl ester of
Examples thereof include vinyl cyanide compounds and ethylenically unsaturated carboxylic acid amides. Of these, the (meth) acrylic acid alkyl ester is particularly useful for improving the coatability.

The amount of component (d) used is 0 to 50% by weight, preferably 0 to 30% by weight, based on all the monomers.

The copolymer latex (A-1) of the present invention
Is obtained by emulsion-polymerizing a specific proportion of the components (a) to (d) using a known emulsifier, polymerization initiator, chain transfer agent and the like.

Here, as the emulsifier, anionic emulsifiers such as sodium dodecylbenzene sulfonate, sodium lauryl sulfate, sodium diphenyl ether disulfonate, sodium succinate dialkyl ester sulfonate, or polyoxyethylene alkyl ester, polyoxyethylene alkyl allyl are used. Examples thereof include nonionic emulsifiers such as ethers, amphoteric emulsifiers, and fluorosurfactants, and one or more of these may be used in combination.

The amount of the emulsifier used is from the monomers (a) to
It is preferably 0.5 to 10 based on the total amount of the component (d).
%, Particularly preferably 1 to 8% by weight. If the amount of the emulsifier used is less than 0.5% by weight, the polymerization stability will be deteriorated, such as coagulation, and the production of the copolymer latex will be hindered, which is not preferable. Since it becomes smaller, the latex viscosity becomes higher, and as a result, the coatability becomes worse.

Further, as the polymerization initiator, persulfate type initiators such as potassium persulfate and ammonium persulfate, or inorganic type initiators such as hydrogen peroxide: cumene hydroperoxide, isopropylbenzene hydroperoxide, paramenthane Examples thereof include organic peroxides such as hydroperoxide and benzoyl peroxide, and organic initiators represented by azo initiators such as azobisisobutyronitrile.

The amount of the polymerization initiator used is preferably 0.03 to 2% by weight, particularly preferably 0.05 to 1% by weight, based on the whole monomer. In order to accelerate emulsion polymerization, for example, sodium pyrobisulfite, sodium sulfite, sodium hydrogen sulfite, ferrous sulfate, glucose, formaldehyde sodium sulfoxylate, L-
Reducing agents such as ascorbic acid and its salts and sodium bisulfite: Chelating agents such as glycine, alanine, and sodium ethylenediaminetetraacetate can be used together.

As the chain transfer agent, α-methylstyrene dimer, terpinolene, α-terpinene, γ-terpinene, dipentene, octyl mercaptan, n-dodecyl mercaptan, t-dodecyl mercaptan, n-hexadecyl mercaptan, diethyl xanthogen disulfide, Dimethylquintogen disulfide, diisopropylxanthogen disulfide, tetramethylthiuram monosulfide, tetraethylthiuram disulfide, tetrabutylthiuram disulfide, dipentamethylthiuram disulfide and the like can be used. These are usually used in an amount of 0 to 15% by weight based on the whole monomer.

The average particle size of the copolymer latex (A-1) used in the present invention is usually 500 to 3,000 angstroms, preferably 1,000 to 2,500 angstroms. The average particle diameter as used herein is a value calculated by treating the copolymer latex with osmic acid, taking an electron micrograph at a magnification of 60,000, measuring the particle diameter of 100 or more particles, and calculating the number average thereof. Is.

When the average particle size of the particles of the copolymer latex (A-1) exceeds 3,000 angstroms, the permeability of the alkaline liquid as an etching agent into the coating film increases and the performance of the maskant deteriorates. On the other hand, if the average particle size is less than 500 Å, the viscosity of the masking composition tends to be high, and the coating properties tend to be poor, which is not preferable.

Furthermore, the copolymer latex (A
The gel content of -1) is usually 20 to 95% by weight, preferably 30 to 85% by weight. The "gel content" here is obtained by dissolving a film obtained by drying a copolymer latex in toluene, separating the insoluble matter by filtration, and further removing toluene from the insoluble matter. The weight ratio of the residual solid content to the total solid content (solid content of the film). When the gel content of the copolymer latex (A-1) exceeds 95% by weight, the permeability of the alkaline solution becomes large, which deteriorates the performance of the maskant. On the other hand, when the gel content is less than 20% by weight, the coating film is soft and the film strength is low, so that the peelability of the maskant becomes poor.

Next, the monomer components (e) to
(Co) polymer latex consisting of (g) (hereinafter "(co)"
The monomer component used for producing the polymer latex (A-2) "will be described.

Examples of the unsaturated carboxylic acid ester as the component (e) include (meth) acrylic acid ester monomers, and specific examples of the acrylic acid ester monomers include methyl acrylate, ethyl acrylate, and acrylic acid. Acid n-butyl, isobutyl acrylate, pentyl acrylate, hexyl acrylate, heptyl acrylate, 2-acrylate
Ethylhexyl, octyl acrylate, n-acrylic acid
Examples thereof include nonyl, isononyl acrylate, decyl acrylate, undecyl acrylate, dodecyl acrylate, n-amyl acrylate, lauryl acrylate, benzyl acrylate, cyclohexyl acrylate and the like. Among these, the use of alkyl acrylate having an alkyl group having 4 to 12 carbon atoms is preferable, ethyl acrylate, n-butyl acrylate and isononyl acrylate are more preferable, and n-butyl acrylate is particularly preferable. Is the use of.

Specific examples of the methacrylic acid ester monomer include methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, pentyl methacrylate, hexyl methacrylate, heptyl methacrylate, 2-ethylhexyl methacrylate. Octyl methacrylate, n-nonyl methacrylate, isononyl methacrylate, decyl methacrylate, undecyl methacrylate, dodecyl methacrylate, n-amyl methacrylate, isoamyl methacrylate, lauryl methacrylate,
Examples thereof include benzyl methacrylate and cyclohexyl methacrylate. Of these, carbon number 4 ~
Preference is given to using methacrylic acid alkyl esters having 12 alkyl groups.

The proportion of the component (e) used is 30 to 100% by weight, preferably 70 to 98% by weight, based on the total monomers.
More preferably, it is 90 to 98% by weight. When the amount of the component (e) used is less than 30% by weight, the coatability is poor, and the coating film is too hard and the releasability is poor, and the workability of removing the maskant is poor.

Examples of the ethylenically unsaturated carboxylic acid as the component (f) include itaconic acid, acrylic acid, methacrylic acid, fumaric acid, maleic acid, maleic anhydride, fumaric anhydride and the like. The preferred component (f) is acrylic acid and methacrylic acid, which can be used alone or in combination of both. These (f) components may be neutralized with an alkali metal such as sodium or potassium, and may be used alone,
Alternatively, two or more kinds can be used in combination.

The amount of the component (f) used is 0 to 10% by weight, preferably 0 to 8% by weight, and more preferably 0.1 to 8% by weight, based on all the monomers. The component (f) is mainly used for obtaining good polymerization stability, but serves to further improve the dimensional accuracy of the maskant. However, (f)
When the amount of the component used exceeds 10% by weight, the water resistance of the coating film is lowered, so that a maskant having excellent alkali resistance cannot be obtained, resulting in lack of practicality.

Other copolymerizable monomers of the component (g) include conjugated diene compounds, aromatic vinyl compounds, vinyl cyanide compounds, amide compounds, hydroxyl group-containing monomers, epoxy group-containing monomers. Body, amino group-containing monomer, dicarboxylic acid anhydride and the like.

Examples of the conjugated diene compound and the aromatic vinyl compound include the same as the monomer component of the copolymer latex (A-1).

Specific examples of the vinyl cyanide monomer include:
Acrylonitrile, α-chloroacrylonitrile, α-
Methoxyacrylonitrile, methacrylonitrile, α-
Examples thereof include chloromethacrylonitrile, α-methoxymethacrylonitrile, and vinylidene cyanide. Of these, acrylonitrile is preferred.

The amount of component (g) used is 0 to 70% by weight, preferably 0 to 25% by weight, and more preferably 0 to 9.9% by weight, based on all the monomers. Component (g) is 70
If it exceeds the weight%, a mask having excellent coatability and peelability cannot be obtained.

The (co) polymer latex (A-2) is obtained by emulsion-polymerizing the above-mentioned monomers (e) to (g) using known emulsifiers, polymerization initiators, chain transfer agents and the like. Is.

As the emulsifier, the polymerization initiator and the chain transfer agent, the same ones as in the case of the copolymer latex (A-1) can be used.

Further, (co) polymer latex (A-2)
The ranges of the average particle diameter and gel content of are the same as those of the copolymer latex (A-1).

Next, a component of the polymer latex for an aqueous maskant of the present invention, a (co) polymer latex having a glass transition temperature of −50 to 50 ° C. by differential scanning calorimetry (DSC) (hereinafter referred to as “(copolymer ) Polymer latex (B) "
Will be described).

The (co) polymer latex (B) is a DSC.
Is a polymer latex having a glass transition temperature (Tg) in the range of −50 to 50 ° C., and a preferable Tg is −40.
It is -10 degreeC. When Tg is lower than -50 ° C, blocking of the masking agent is increased and workability is deteriorated. Tg is 5
If the temperature is higher than 0 ° C, the peelability of the maskant becomes poor and the workability deteriorates.

Preferred as (co) polymer latex (B) are urethane polymer latex, vinyl acetate polymer latex, silicone polymer latex, fluorine polymer latex, vinylidene chloride polymer latex, and chloride. Examples thereof include vinyl polymer latex, natural rubber latex and polyisoprene latex. The following effects can be obtained by using these latexes,
A composition for a maskant having various properties improved is obtained, and by appropriately combining these latexes,
A wider range of good characteristics can be obtained. (A) Urethane polymer latex: It imparts excellent mascant strength and heat resistance to the resulting aqueous copolymer latex for a mascant. (B) Vinyl acetate-based polymer latex: The cost can be reduced without deteriorating the performance of the obtained copolymer latex for an aqueous maskant.

Examples of vinyl acetate polymers include vinyl acetate homopolymers and vinyl acetate-ethylene copolymers. (C) Silicone-based polymer latex: It imparts excellent water resistance and releasability to the resulting aqueous copolymer latex for a maskant.

As the silicone polymer latex,
Examples thereof include silicone alone, a copolymer with an acrylic monomer, or a material containing an acrylic polymer. (D) Fluorine-based polymer latex: It imparts excellent heat resistance and maskant strength to the obtained copolymer latex for an aqueous maskant.

Examples of the fluoropolymer latex include vinylidene fluoride homopolymers and copolymers with other monomers. (V) Vinylidene chloride-based polymer latex: It imparts excellent water resistance and leveling property of the maskant to the obtained copolymer latex for an aqueous maskant. (F) Vinyl chloride-based polymer latex: The cost can be reduced without deteriorating the performance of the obtained copolymer latex for an aqueous maskant. (G) Natural rubber latex: It imparts excellent film strength, releasability of the maskant, and workability of removing the maskant to the resulting aqueous latex copolymer for maskant. (H) Polyisoprene-based rubber latex: It imparts the same properties as when natural rubber latex is used.

The stock solution of natural rubber latex is a sol in which rubber particles are dispersed in serum, and the rubber content in the latex is generally 30 to 40% by weight.
That is, it contains proteins, sugars, resins, amino acids, enzymes and the like, and some of these are intricately bound to rubber particles. The natural rubber latex is usually concentrated in an amount sufficient to withstand the long-term storage and transportation of the concentrated latex by centrifuging the stock solution of the natural rubber latex to concentrate the rubber content to 60 to 70% by weight. It is made up of ammonia and other preservatives.

The polyisoprene rubber latex contains isoprene as a main component, and contains other monomers such as an aliphatic conjugated diene compound, an aromatic vinyl compound, an ethylenically unsaturated carboxylic acid and an ethylenically unsaturated carboxylic acid ester. If necessary, a small amount may be copolymerized.

In the present invention, the (co) polymer latex (B) may be used in combination of two or more kinds.

Particularly, as the (co) polymer latex (B), it is preferable to combine natural rubber latex and / or polyisoprene latex and two kinds of latex other than natural rubber latex and polyisoprene latex.

When the copolymer latex (A-1) is used, the (co) polymer latex (A-2) is (co).
It is possible to use as the polymer latex (B), and when using the (co) polymer latex (A-2), the copolymer latex (A-1) is used as the (co) polymer latex (B). It is also possible to use as.

The copolymer latex for an aqueous maskant according to claim 1 of the present invention is the copolymer latex (A-1).
From 5 to 95% by weight in terms of solid content and 95 to 5% by weight of the (co) polymer latex (B) in terms of solid content, preferably the copolymer latex (A-1) is in solid form. It is composed of 30 to 70% by weight in terms of minutes and 70 to 30% by weight of the (co) polymer latex (B) in terms of solids.

If the amount of the (co) polymer latex (B) used is less than 30% by weight or more than 70% by weight, the releasability of the mask is poor.

Further, the copolymer latex for an aqueous maskant according to claim 2 of the present invention comprises the (co) polymer latex (A-2) in an amount of 5 to 100% by weight in terms of solid content. Latex (B) 95 to 0 in terms of solid content
% By weight, preferably 30 to 70% by weight of the (co) polymer latex (A-2) in terms of solid content and 70% by weight of the (co) polymer latex (B) in terms of solid content.
.About.30% by weight.

The copolymer latex of the present invention comprises a filler,
A composition for an aqueous maskant can be prepared by blending with an additive such as a thickener, a film-forming agent, a defoaming agent and a film-forming auxiliary.

[0054]

The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. In the following description, "parts" and "%" indicate parts by weight and% by weight. (Examples 1 to 10 and Comparative Examples 1 to 5) Production of copolymer latex (A-1) 100 parts of monomer shown in Table 1, 3 parts of sodium dodecylbenzenesulfonate, 5 parts of t-dodecyl mercaptan, 0.5 parts of ammonium sulfate, 0.01 parts of sodium ethylenediamine tetraacetate and 150 parts of water were charged into a 100-liter stainless steel reactor at a polymerization temperature of 40-
Emulsion polymerization was carried out at 60 ° C. for 20 hours to produce copolymer latexes (a) and (a). The polymerization conversion rates were all 98% or more. Production of copolymer latex (A-2) 100 parts of monomer shown in Table 1, 3 parts of sodium dodecylbenzenesulfonate, t-dodecyl mercaptan 0.3
Parts, ammonium persulfate 0.5 parts, sodium ethylenediaminetetraacetate 0.01 parts and water 150 parts
The mixture was charged into a 00 liter reactor made of stainless steel, and emulsion polymerization was carried out at a polymerization temperature of 60 to 80 ° C. for 8 hours to produce copolymer latexes (c) and (d). The polymerization conversion rates were all 98% or more.

[Table 1] Method for preparing composition for aqueous maskant Copolymer latex (A-1) or copolymer latex (A-2) obtained by the above method and (co) polymer latex (B) for aqueous maskant Water was added to the polymer latex using the components and blending amounts shown in Tables 2 and 3 so that the solid content was 50%, and the mixture was stirred.
A composition for an aqueous maskant was prepared.

[Table 2]

[Table 3] The physical properties of the obtained composition for aqueous maskant were evaluated by the following methods, and the evaluation results are shown in Tables 2 and 3. Evaluation of Physical Properties of Aqueous Mascant Composition Coating Property An aluminum substrate was dipped in each of the obtained aqueous maskants compositions, dried at room temperature, and heat-treated at 80 ° C. for 60 minutes to form a test piece. 90 ℃ in alkaline solution
The state of the coating film after immersing for 3 hours was observed. When the coating film was extremely uniformly formed, it was marked with ⊚, when the coating film was formed uniformly, was marked with ◯, and when the coating film had unevenness, blisters, and cracks, it was marked with x. Peelability An aluminum substrate was dipped in the obtained aqueous composition for amascant to form a coating film having a film thickness of 400 to 600 µm, and a test piece was obtained. This test piece was treated with an alkaline aqueous solution (3 at 90 ° C).
After immersing in water for 2 hours, wash with water and dry. Then, the coating film was peeled by hand to determine the peelability.

If the peeling strength of the maskant is too large, the workability (peeling property) of removing the mask after etching is poor, while if the peeling strength is too small, the adhesion of the maskant to the substrate becomes insufficient. Regarding the releasability, the state in which the maskant can be easily peeled off with a finger without impairing the adhesiveness was marked with ◯, and the one excellent in this property was marked with ◎. Moreover, when it was difficult to peel off the maskant or when the adhesiveness of the maskant to the substrate was insufficient, it was marked with x. Alkali resistance An aluminum substrate was masked with an aqueous maskant composition to form a coating film having a thickness of 400 μm, and a test piece was obtained. After immersing this test piece in an alkaline aqueous solution (90 ° C. for 2 hours), the surface condition of the coating film was observed. If the surface condition before immersion is maintained, it is evaluated as ◯, and if the surface smoothness after immersion is reduced and swelling occurs, it is evaluated as ×.

This alkali resistance is one of the indexes of the dimensional accuracy of the maskant. Heat resistance An aluminum substrate was masked with an aqueous maskant composition to form a coating film having a film thickness of 400 μm, and a test piece was obtained. Set this test piece in the gear aging tester and
Heat is applied at 0 ° C. for 2 hours. If the surface condition of the coating film before heating and the hardness by touching with the finger are almost completely maintained, it is marked with ◎, and if it is almost maintained, it is marked with ○, the surface condition changes after heating, or the hardness by touching becomes large. The case was marked as x. Tensile strength Aqueous mascant composition is dried on a glass plate to a dry film thickness of 350 μ
m, and after standing at room temperature for 1 day or more, preferably 2 to 3 days, the film is peeled from the glass plate surface and heat-treated at 120 ° C. for 30 minutes. The film after this treatment is JIS
It was measured according to the tensile test in the physical test method for vulcanized rubber of K6301.

The aqueous mascant compositions of Examples 1 to 10 are examples using the latex for an aqueous mascant of the present invention, and the effects of the object of the present invention are obtained.

Comparative Examples 1 to 5 are copolymer latexes (A
-1), the copolymer latex (A-2) or the (co) polymer latex (B) alone is an example of producing an aqueous maskant composition, and it can be seen that one of the composition properties is inferior.

[0059]

EFFECTS OF THE INVENTION By using the latex for aqueous mascant according to the present invention, it has a wide range of properties and is excellent in film strength in etching, dimensional accuracy of mascant, coating property and workability of removing mascant, and it is suitable for environment such as air pollution. It is possible to provide an aqueous maskant composition that does not cause health and safety problems.

Therefore, according to the present invention, it is possible to provide a latex for an aqueous maskant having an extremely high industrial value.

Claims (2)

[Claims] 1. An (a) aliphatic conjugated diene compound 3
0 to 70% by weight, (b) aromatic vinyl compound 20 to 70% by weight, (c) ethylenically unsaturated carboxylic acid 0 to 10% by weight, (d) other copolymerizable monomer 0 to 50% by weight %, A copolymer latex obtained by emulsion polymerization of a monomer consisting of 5 to 95% by weight (in terms of solid content), and a glass transition temperature by differential scanning calorimetry of -50 to 5
A copolymer latex for an aqueous maskant containing 95 to 5% by weight (in terms of solid content) of a (co) polymer latex at 0 ° C. 2. (e) Unsaturated acrylic acid ester 3
0-100 wt%, (f) ethylenically unsaturated carboxylic acid 0-10 wt%, (g) other copolymerizable monomer 0-70 wt%, obtained by emulsion polymerization of a monomer. 5 to 100% by weight (solid content) of the (co) polymer latex obtained, and a glass transition temperature of -50 to 5 by differential scanning calorimetry.
A copolymer latex for an aqueous maskant, which contains 95 to 0% by weight (in terms of solid content) of a (co) polymer latex at 0 ° C.