KR101687801B1 - Resin for antifouling coating with improved erosion rate and antifouling coating composition comprising the same - Google Patents

Abstract

The present invention relates to a resin for an antifouling paint having an improved abrasion rate and an antifouling paint composition comprising the same, and more particularly to a resin containing an anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer as a specific polymerized unit, And an anti-corrosive coating composition comprising the resin and having an improved wear rate.

Description

Technical Field [0001] The present invention relates to a resin for an antifouling paint having improved abrasion rate and an antifouling coating composition containing the same,

The present invention relates to a resin for an antifouling paint having an improved abrasion rate and an antifouling paint composition comprising the same, and more particularly to a resin containing an anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer as a specific polymerized unit, And an anti-corrosive coating composition comprising the resin and having an improved wear rate.

Antifouling paints are applied to the coating of the ship's hull and underwater structures to prevent the attachment and growth of marine life. When various marine organisms are attached to the surface of the film, the frictional force between the surface of the coating and the seawater increases during operation of the vessel, which may increase the fuel cost significantly. The antifouling coating removes such adherence to reduce the coefficient of friction between the water and the ship Lt; / RTI >

Korean Patent Publication No. 1997-7004840 discloses a method of mixing a plastic (meth) acrylate copolymer in order to solve the problem of a copolymer composed of trimethylsilyl (meth) acrylate monomer. However, in this case, There is a problem in that the abrasion rate is gradually decreased as the non-hydrolyzable binder remains.

JP-A-2010-150355 discloses an antifouling paint in which acrylic acid, methacrylic acid, triisopropylacrylate or the like is applied as a hydrolysis element to a binder resin in order to improve the long-term wear rate, but the effect of improving the wear rate is not sufficient.

SUMMARY OF THE INVENTION The present invention has been made to overcome the problems of the prior art as described above, and it is an object of the present invention to provide a resin containing an anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer as a specific polymerized unit, It is a technical object to provide a coating composition.

In order to solve the above-mentioned technical problems, the present invention relates to a polyalkylene glycol mono (meth) acrylate oligomer having (1) an anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer; (2) a monomer containing a double bond and a silyl group; (3) a monomer containing a double bond and a carboxylic acid group; And (4) a monomer comprising a double bond and an alkyl group.

According to another aspect of the present invention, there is provided an antifouling paint composition comprising the reaction product of the copolymer resin of the present invention, a divalent metal cation, and an organic carboxylic acid having a molecular weight of 1000 or less.

Since the copolymer resin according to the present invention and the antifouling paint composition containing the same exhibit remarkably improved abrasion rate as compared with the conventional product, it is possible to prevent adhesion and growth of marine life as a top coat of the paint applied to the hull and underwater structure of the ship And can be particularly suitably used for the purpose of the present invention.

Hereinafter, the present invention will be described in detail.

The copolymer resin of the present invention comprises an anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer as polymerized units.

The anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer may be obtained by reacting polyalkylene glycol mono (meth) acrylate with an acid anhydride. Preferred polyalkylene glycol mono (meth) acrylates include at least one poly (C ₂ -C ₄ ) alkylene glycol mono (meth) acrylate, more preferably represented by the following general formula May be used.

[Chemical Formula 1]

In the above, R1 and R2 are each independently H or CH _3, m is an integer from 1 to 22.

(2)

R 3, R 4 and R 5 are each independently H or CH ₃ , and n and o are each independently an integer of 1 to 22.

The acid anhydrides which react with the polyalkylene glycol mono (meth) acrylate are preferably C ₂ to C ₂₄ aliphatic acid anhydrides, C ₄ to C ₂₄ alicyclic oxalic anhydrides, and C ₇ to C ₂₄ aromatic acid anhydrides , And more preferably at least one selected from the group consisting of succinic anhydride, maleic anhydride, dodecylsuccinic anhydride, octylsuccinic anhydride, phthalic anhydride, hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, tetrahydrophthalic anhydride , Methyltetrahydrophthalic anhydride, pyromellitic dianhydride (PMDA), 3,3 ', 4,4-oxydiphthalic dianhydride (ODPA), 3,3', 4,4'-benzophenonetetracarboxylic acid Dianhydride (6FDA), benzoquinonetetracarboxylic acid dianhydride, ethylene tetracarboxylic acid dianhydride, and (meth) acrylate dianhydride (BTDA), 4,4'-diphthalic acid (hexafluoroisopropylidene) anhydride ) It can be used at least one selected from the group consisting of acrylic anhydride.

There is no particular limitation on the amount of the acid anhydride used in the reaction with the polyalkylene glycol mono (meth) acrylate, and for example, 1 mole of the acid anhydride per mole of the polyalkylene glycol mono (meth) acrylate can be used. Specifically, if the amount of the acid anhydride to be used is too small, the carboxyl group group is relatively reduced, which may cause a problem that the coupling ratio with the metal oxide is changed during the second reaction. On the contrary, if the amount of the acid anhydride is excessively large, the acidic acid remaining after bonding is formed, so that the metal oxide reacts with the low molecular weight anhydride during the second reaction, and the physical properties of the coating may be lowered.

The reaction of the polyalkylene glycol mono (meth) acrylate and the acid anhydride can be carried out under generally known conditions and can be carried out under elevated temperature conditions, for example 70 to 110 DEG C, in the presence of a suitable catalyst such as butylated hydroxytoluene, ), But is not limited thereto.

The resulting anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer preferably has a molecular weight of from 400 to 1000, an acid value (based on solids) of from 50 to 200 mg KOH / g, and a Gardner viscosity of U or T ).

The amount of the anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer contained as a polymerization unit in 100 parts by weight of the copolymer resin of the present invention may be preferably 5 to 30 parts by weight. When the amount of the anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer is less than the above range, there is a problem that the abrasion rate of the coating film is lowered, and if it is more than this amount, the crack resistance of the coating film is lowered, There may be a problem of speeding up.

In addition, the copolymer resin of the present invention includes, as polymerized units, monomers containing a double bond and a silyl group capable of hydrolysis. The monomer containing the double bond and the silyl group is preferably at least one mono-, di- or tri (C ₁ -C ₆ ) alkylsilyl (meth) acrylate, more preferably trimethylsilyl acrylate, trimethyl At least one selected from the group consisting of silyl methacrylate, triisopropylsilyl acrylate, triisopropylsilyl methacrylate, tributylsilyl acrylate and tributylsilyl methacrylate can be used.

The amount of the monomer containing a double bond and a silyl group contained as a polymerization unit in 100 parts by weight of the copolymer resin of the present invention may be preferably 10 to 40 parts by weight. If the amount of the monomer containing a double bond and a silyl group is less than the above range, there is a problem that the antifouling property is poor, and if it exceeds this amount, the abrasion rate is lowered and the cost may be increased.

In addition, the copolymer resin of the present invention comprises a monomer containing a double bond and a carboxylic acid group as polymerized units. As the monomer containing a double bond and a carboxylic acid group, there may be used (meth) acrylic acid, or a monomer prepared by a ring-opening reaction of a monomer containing a double bond and an alcohol group and an acid anhydride monomer. Examples of the monomer containing the double bond and the alcohol group include C ₂ -C ₁₂ hydroxyalkyl (meth) acrylates, preferably 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) , At least one selected from the group consisting of hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, hydroxybutyl (meth) acrylate, have. As the acid anhydride, those described above can be used.

The amount of the monomer containing a double bond and a carboxylic acid group contained as a polymerization unit in 100 parts by weight of the copolymer resin of the present invention may be preferably 10 to 40 parts by weight. If the amount of the monomer containing a double bond and a carboxylic acid group is less than the above range, there may be a problem that the discoloration resistance to heat and the wear rate are lowered, and if it is more than this range, there is a problem that the crack resistance is poor.

In addition, the copolymer resin of the present invention includes a monomer containing a double bond and an alkyl group as polymerized units. As the monomer containing a double bond and an alkyl group, at least one selected from the group consisting of alkyl (meth) acrylate, cycloalkyl (meth) acrylate and bicycloalkyl (meth) acrylate can be used. preferably consisting of (C ₁ -C ₁₂₎ alkyl (meth) acrylate, (C ₃ -C ₁₂₎ cycloalkyl (meth) acrylate, (C ₇ -C ₁₂₎₎ bicyclo (meth) acrylate (Meth) acrylate, n-butyl (meth) acrylate, n-hexyl (meth) acrylate, cyclohexyl (meth) acrylate, (Meth) acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate and isobonyl (meth) acrylate.

The amount of the monomer containing a double bond and an alkyl group contained as a polymerization unit in 100 parts by weight of the copolymer resin of the present invention may be preferably 30 to 60 parts by weight. If the amount of the monomer containing a double bond and an alkyl group is less than the above range, it is difficult to control the Tg. Therefore, the copolymer resin of the present invention can be prepared by polymerizing the above monomer components by a conventional radical polymerization method have. The solvent which can be used in the radical polymerization reaction is not particularly limited so long as it does not adversely affect the reaction, but aromatic solvents such as toluene and xylene, methyl ethyl ketone, methyl propyl ketone, methyl butyl ketone, ethyl propyl ketone, Methyl acetate, isopropyl acetate, isopropyl acetate, butyl acetate, methyl cellosolve acetate, cellosolve acetate, butyl cellosolve, methyl cellosolve acetate, ethyl cellosolve acetate, Acetate, and carbitol acetate; alcoholic solvents such as n-propanol, isopropanol, n-butanol, isobutanol, and tertiary butanol may be used. The radical polymerization reaction can be carried out in this solvent under reflux.

Preferably, the solid content of the copolymer resin of the present invention is 10% or more and less than 90%, and the acid value (based on solid content) is 50 to 225 mgKOH / g. If the solid content of the copolymer resin is too low, the abrasion rate and discoloration resistance of the coating film may be lowered. On the other hand, if the solid content is too large, the reaction temperature control may not be controlled well. If the acid value of the copolymer resin is less than 50 mgKOH / g, the abrasion rate, antifouling property and discoloration resistance of the coating film may be lowered. If the acid value exceeds 225 mgKOH / g, the crack resistance of the coating film is lowered, There may be a problem.

According to another aspect of the present invention, there is provided an antifouling paint composition comprising the reaction product of the copolymer resin of the present invention, a divalent metal cation, and an organic carboxylic acid having a molecular weight of 1000 or less. The reaction of the copolymer resin, the divalent metal cation, and the organic carboxylic acid having a molecular weight of 1000 or less is a condensation reaction.

The divalent metal cation has a role of generating a bond that enables the coating film to be abraded by hydrolysis in seawater. Preferably, the divalent metal cation is one selected from the group consisting of Zn ^{2 +} , Cu ^{2 +} , Mn ^{2 +,} and Co ^{2 +} But is not limited thereto.

As the organic carboxylic acid having a molecular weight of 1000 or less, at least one selected from the group consisting of aliphatic acids, alicyclic acids and aromatic acids containing at least one carboxylic acid group (for example, 1 to 4) Preferably at least one selected from the group consisting of C ₂ to C ₂₄ aliphatic acids, C ₄ to C ₂₄ alicyclic acids and C ₇ to C ₂₄ aromatic acids can be used. Examples of the organic acid include acetic acid, formic acid, acetic acid, chloroacetic acid, dichloroacetic acid, trichloroacetic acid, trifluoroacetic acid, benzoic acid, naphthenic acid, succinic acid, malonic acid, oxalic acid, glutaric acid, adipic acid, At least one selected from the group consisting of lauric acid, glycolic acid, citric acid, phthalic acid, isophthalic acid and terephthalic acid can be used. Alternatively, a half ester resulting from the reaction of an acid anhydride with an alcohol may be used. As the acid anhydride, those described above can be used. The alcohol may be selected from the group consisting of C ₁ to C ₁₂ aliphatic alcohols containing one or more (for example, 1 to 4) hydroxyl groups, C ₃ to C ₁₂ alicyclic alcohols and C ₆ to C ₁₂ aromatic alcohols Can be used. Examples of the solvent include ethylene glycol, propylene glycol, trimethylol propane, trimethylol ethane, 1,6-hexanediol, diethylene glycol, dipropylene glycol, triethylene glycol, 1,3-butylene glycol, (Meth) acrylate, 2-hydroxypropyl (meth) acrylate, hydroxyisopropyl (meth) acrylate, 2-hydroxypropyl (Meth) acrylate, butanediol mono (meth) acrylate, 4-hydroxybutyl (meth) acrylate and caprolactone (meth) acrylate.

The condensation reaction of the copolymer resin, the divalent metal cation and the organic carboxylic acid having a molecular weight of 1000 or less can be carried out under a generally known condition and can be carried out in a suitable solvent as described above under reflux However, the present invention is not limited thereto.

The antifouling paint composition of the present invention may further contain at least one additive component that can be commonly used in an antifouling paint, in addition to the reaction product of the copolymer resin, the divalent metal salt and the organic carboxylic acid having a molecular weight of 1000 or less. Examples of such additives include antifouling agents in the form of organic or inorganic compounds, organic or inorganic pigment components (for example, titanium white, red iron oxide, organic red pigment, talc, etc.), anti-sagging agents, , Various resins such as plasticizers, acrylic resins and polyalkyl vinyl ethers (vinyl ether (co) polymers), defoaming agents, and the like, but are not limited thereto.

In addition, the antifouling paint composition of the present invention may further comprise an elution regulator component that serves to control the elution rate of the antifouling agent together with the controlled abrasion behavior of the coating film in seawater. As the elution regulator component, at least one selected from the group consisting of rosin, rosin derivatives, monocarboxylic acids and salts thereof can be used. Examples of the rosin include rosin, rosin and tall oil rosin. Examples of the rosin derivative include (low melting point) disintegrating rosin, hydrogenated rosin, polymerized rosin, rosin and rosin derivative metal salts Salts, zinc salts or magnesium salts) and rosin amines. The rosin and rosin derivatives may be used singly or in combination of two or more. Examples of the monocarboxylic acid include a fatty acid having 5 to 30 carbon atoms or naphthenic acid. It is preferable that the elution regulator is contained in an amount of 0.1 to 25% by weight (in terms of solid content) based on the total weight of the antifouling paint composition, and the compounding ratio thereof can be determined from the viewpoints of the antifouling performance and the water resistance performance of the coating film.

Hereinafter, the present invention will be described in more detail with reference to Examples. However, the scope of the present invention is not limited to these examples.

[ Example ]

Manufacturing example  One: Anhydrous  denaturalization Polyalkylene  Glycol Mono (meth) acrylate Oligomer  One

Thermometer and a cooler under a four-necked flask in a nitrogen atmosphere having a polyethylene glycol monomethacrylate (in formula _{1 R1 = CH 3, R2 =} H, m = 11) 820g, butylated hydroxytoluene 1.0g, hexa hydro rope 345 g of tallic anhydride was added, the temperature was raised to 90 캜 and maintained for 6 hours. A light brown transparent oligomer 1 having an acid value of 108 mg KOH / g and a Gardner viscosity (25 캜) U was obtained.

Manufacturing example  2: Anhydrous  denaturalization Polyalkylene  Glycol Mono (meth) acrylate Oligomer  2

Except that 770 g of polyethylene glycol monoacrylate (R 1 = H, R 2 = H, m = 5 in the formula (1)) was added in the above Production Example 1 to obtain an acid value of 115 mgKOH / g , A Gardner Viscosity (25 占 폚) U, was obtained.

Manufacturing example  3: Anhydrous  denaturalization Polyalkylene  Glycol Mono (meth) acrylate Oligomer  3

Except that 1270 g of polyethylene glycol monoacrylate (R 1 = H, R 2 = H, m = 11 in the formula (1)) was added in the above Production Example 1 to obtain an acid value of 78 mgKOH / g, and a Gardner viscosity (25 캜) T.

Manufacturing example  4: Anhydrous  denaturalization Polyalkylene  Glycol Mono (meth) acrylate Oligomer  4

In Production Example 1, except that 818 g of polyalkylene glycol monomethacrylate (R3 = CH3, R4 = CH3, R5 = H, n = 3, o = 5 in Chemical Formula 2) , A light brown transparent oligomer 4 having an acid value of 108 mgKOH / g and a Gardner viscosity (25 ° C) O was obtained.

Comparative Example  One

A thermometer and a condenser, 300 g of butanol and 300 g of xylene were charged in a nitrogen atmosphere, and the mixture was heated to 120 DEG C and refluxed. A mixed solution prepared by mixing 175 g of methacrylic acid, 340 g of ethyl acrylate, 335 g of butyl acrylate, 150 g of triisopropylsilyl acrylate, 150 g of tertiary amyl peroxyhexanoate as an initiator and 350 g of xylene was stirred for 4 hours The mixture was uniformly added dropwise, refluxed for 2 hours, and cooled to 60 ° C to prepare a binder resin.

446 g of naphthenic acid, 164 g of zinc oxide, 300 g of xylene and 36 g of ionized water were added to the resin thus prepared, and the temperature was raised to a reflux temperature of 100 캜. The mixture was refluxed at 100 ° C for 5 hours to obtain a brown transparent reaction product having a solid content of 55.3% and a Gardner viscosity (25 ° C) Y.

Comparative Example  2

A thermometer and a condenser, 300 g of butanol and 300 g of xylene were charged in a nitrogen atmosphere, and the mixture was heated to 120 DEG C and refluxed. A mixed solution obtained by mixing 175 g of methacrylic acid, 675 g of butyl acrylate, 150 g of triisopropylsilyl acrylate, 150 g of tertiary amyl peroxyhexanoate as an initiator and 350 g of xylene was uniformly added dropwise over 4 hours, Refluxed for 2 hours, and then cooled to 60 DEG C to prepare a binder resin.

446 g of naphthenic acid, 164 g of zinc oxide, 300 g of xylene and 36 g of ionized water were added to the resin thus prepared, and the temperature was raised to a reflux temperature of 100 캜. The mixture was refluxed at 100 ° C for 5 hours to obtain a brown transparent reaction product having a solid content of 55.3% and a Gardner viscosity (25 ° C) I.

Example  One

A thermometer and a condenser, 300 g of butanol and 300 g of xylene were charged in a nitrogen atmosphere, and the mixture was heated to 120 DEG C and refluxed. 150 g of the oligomer (oligomer 1) of Production Example 1, 140 g of methacrylic acid, 240 g of methyl methacrylate, 290 g of butyl acrylate, 145 g of triisopropylsilyl acrylate, 150 g of tertiary amyl peroxyhexanoate as an initiator, And 350 g of xylene were separately added dropwise for 4 hours, refluxed for 2 hours, and cooled to 60 ° C to prepare a binder resin.

435 g of naphthenic acid, 160 g of zinc oxide, 150 g of xylene and 45 g of ionized water were added to the resin thus prepared, and the temperature was raised to a reflux temperature of 100 캜. And refluxed at 100 ° C for 5 hours to obtain a brown transparent reaction product having a solid content of 55.3% and a Gardner viscosity (25 ° C) Z

Example  2

In Example 1, an oligomer (oligomer 2) of Preparation Example 2 was used in place of the oligomer of Production Example 1, 150 g of the oligomer 2, 140 g of methacrylic acid, 250 g of methyl methacrylate, 300 g of butyl acrylate, Acrylate obtained in Example 1 was used in the same manner as in Example 1 to obtain a brown transparent reaction product having a solid content of 55.3% and a Gardner viscosity (25 DEG C) of Z. [

Example  3

In Example 1, the oligomer (oligomer 3) of Production Example 3 was used in place of the oligomer of Production Example 1, and 215 g of the oligomer 3, 140 g of methacrylic acid, 245 g of methyl methacrylate, 225 g of butyl acrylate, Except that 145 g of acrylate was added, a brown transparent reaction product having a solid content of 55.3% and a Gardner viscosity (25 캜) Y was obtained.

Example  4

330 g of butanol and 330 g of xylene were charged into a four-necked flask equipped with a stirrer, a thermometer and a condenser, and the mixture was heated to 120 DEG C and refluxed. To this were added 300 g of the oligomer (oligomer 4) of Production Example 4, 150 g of methacrylic acid, 220 g of methyl methacrylate, 195 g of butyl acrylate, 165 g of triisopropylsilyl acrylate, 150 g of tertiary amyl peroxyhexanoate as an initiator, And 400 g of xylene were each added dropwise uniformly for 4 hours, refluxed for 2 hours and cooled to 60 ° C to prepare a binder resin.

465 g of naphthenic acid, 170 g of zinc oxide, 200 g of xylene and 45 g of ionized water were added to the resin thus prepared, and the temperature was raised to 100 캜 at the reflux temperature. And refluxed at 100 ° C for 5 hours to obtain a brown transparent reaction product having a solid content of 55.3% and a Gardner viscosity (25 ° C) of Z1

Antifouling paint  Preparation of composition

An antifouling paint composition comprising the reaction products prepared in Comparative Examples 1 to 2 and Examples 1 to 3 as a binder component was prepared as shown in Table 1 below and its properties were evaluated and shown in Table 2 below.

The evaluation method of the physical properties of the antifouling paint composition is as follows.

Paint solid

1) Test conditions: about 3.0 g of the prepared coating, sampling at 150 ° C for 24 hours

2) Solid (%): weight after heating / weight before heating × 100

Paint viscosity

Test conditions: Measurement at 25 ° C, Kreb's Unit

Press  exam

1) Specimen: 100 × 300 × 3 (mm) Steel plate

2) Specimen treatment: sandblasting → epoxy system paint 150 ㎛ → epoxy binder paint 100 ㎛ (after drying each painting and drying at room temperature (20 ℃) for 1 day)

3) Antifouling paint: 300 ㎛ After painting 1 week Dry at room temperature (20 ℃)

4) Test conditions: 20 × 20 × 20 (mm) Stress after 50 kgf / ㎤ pressure for 40 minutes

5) Strain (%): 100- (film thickness after application of pressure / film thickness before applying pressure)

6) Evaluation Criteria

5: Strain less than 3%

4: Strain less than 3 ~ 5%

3: strain less than 5 ~ 7%

2: strain less than 7 ~ 10%

1: Strain more than 10%

Crack resistance  exam

1) Specimen: 100 x 300 x 1.5 (mm)

2) Specimen treatment: sandblasting → epoxy system paint 150 ㎛ → epoxy binder paint 100 ㎛ (after drying each painting and drying at room temperature (20 ℃) for 1 day)

3) Antifouling paint: 600 ㎛ After painting 1 week Dry at room temperature (20 ℃)

4) Test conditions: 23 ℃ sea water 24 hours immersion → 24 hours outdoor drying - 30 times repeated

5) Evaluation Criteria

5: No cracks or visible defects

4: Less than 5% of the total area of test specimen cracked.

3: Crack occurs in less than 5 ~ 20% of the total area of test specimen.

2: Less than 20 to 50% of the total area of the specimen cracked.

1: Crack occurs at 50 ~ 70% of the total area of test specimen

0: Crack occurs at 70% or more of the total area of test specimen

Antifouling performance  exam

1) Specimen: 550 × 150 × 2 (mm) Steel plate

2) Specimen treatment: Sandblasting → Epoxy system paint 200㎛ → Epoxy binder paint 100㎛ (Each paint is dried and dried at room temperature (20 ℃) for 1 day)

3) Antifouling paint: 300 ㎛ After painting 1 week Dry at room temperature (20 ℃)

4) Test conditions: 1 m below the sea level in a raft type test equipment installed on the coast of Ulsan (east coast) and Geoje Island (south coast)

5) Evaluation Criteria

5: In the absence of marine organisms (non-polluted)

4: A state in which a thin slime layer is observed

3: A thick slime layer is observed or the vegetable contamination area is less than 20% of the effective area of the specimen

2: The condition that the vegetable contamination area exceeds 20% to 50% of the effective area of the specimen

1: The condition that the vegetable contamination area exceeds 50% to 100% of the effective area of the specimen

X: Animal contamination occurred

My discoloration property  Measure

1) Specimen: 150 x 70 x 3 (mm) Glass Specimen

2) Sample preparation: XL washing and drying

3) Antifouling paint: 250 ㎛ After painting 1 week Dry at room temperature (20 ℃)

4) Test conditions: After immersing in fresh water container, after removing a certain amount of fresh water at intervals of 1 day, observed discoloration degree, visual judgment - 14 days observation

5) Evaluation criteria: 5 (good) ~ 1 (bad)

Wear rate (탆 / month )

1) Specimen: 150 × 70 × 1 (mm) Stainless steel plate

2) Specimen treatment: Sandblasting Epoxy system → epoxy system paint 50㎛ → sealer coat 50㎛

3) Antifouling paint: 100 ㎛ is coated at intervals of one day and then dried for one week at room temperature (20 ℃)

4) Test conditions: It was installed on the outside of a rotating drum having a diameter of 600 (mm) and a height of 300 (mm), then rapidly rotated at a rate of 25 (knot) under a constant temperature condition of 25 ° C, The wear rate (wear rate) was evaluated by measuring the change.

The abrasion rate in the present invention means the thickness (탆 / month) of the coating film cut out for one month (30 days). If the abrasion rate is low, it is not preferable because a barnacle can adhere to the surface of the ship even if it contains an antifouling agent. As shown in Table 2, the abrasion rate (about 8 占 퐉 / month), which is twice as high as the abrasion rate (4 占 퐉 / month) of the comparative example in the case where the anhydrous modified polyalkylene glycol mono (meth) acrylate oligomer of the present invention was applied, / month). This is considered to be because the COOH functional group can be elongated out of the conventional methacrylic acid only (comparative example), so that the interference of other molecules is reduced and the wear rate can be improved. Accordingly, it has been confirmed that the antifouling paint to which the anhydrous acid-modified polyalkylene glycol monoacrylate oligomer of the present invention is applied can be suitably used to prevent the attachment and growth of marine organisms as a top coat of the coating film applied to the ship ' Respectively.

Claims (5)

As polymerized units, (1) a nonaqueous acid modified polyalkylene glycol mono (meth) acrylate oligomer; (2) a monomer containing a double bond and a silyl group; (3) a monomer containing a double bond and a carboxylic acid group; And (4) a monomer containing a double bond and an alkyl group,
Wherein the anhydride-modified polyalkylene glycol mono (meth) acrylate oligomer is obtained by the reaction of a polyalkylene glycol mono (meth) acrylate and an acid anhydride,
Wherein the polyalkylene glycol mono (meth) acrylate is at least one represented by the following formula (1) or (2):
[Chemical Formula 1]

(2)

In the above, R1 to R5 are each independently H or CH _3, and, m, n and o are each independently an integer from 1 to 22. The copolymer according to claim 1, wherein the acid anhydride is at least one selected from the group consisting of C ₂ to C ₂₄ aliphatic acid anhydrides, C ₄ to C ₂₄ alicyclic oxalic anhydrides, and C ₇ to C ₂₄ aromatic acid anhydrides. Suzy. delete The method according to claim 1,
Monomer is one or more mono-containing group and the double bond silyl, di-or tri-and (C ₁ -C ₆₎ alkylsilyl (meth) acrylate,
Wherein the monomer containing a double bond and a carboxylic acid group is a monomer prepared by a ring-opening reaction of a (meth) acrylic acid or a monomer containing a double bond and an alcohol group and an acid anhydride monomer,
Wherein the monomer containing the double bond and the alkyl group is selected from the group consisting of (C ₁ -C ₁₂ ) alkyl (meth) acrylate, (C ₃ -C ₁₂ ) cycloalkyl (meth) acrylate and (C ₇ -C ₁₂ ) bicycloalkyl (Meth) acrylate, and at least one selected from the group consisting of
Copolymer resin. An antifouling paint composition comprising the reaction product of the copolymer resin of any one of claims 1, 2, and 4, a divalent metal cation, and an organic carboxylic acid having a molecular weight of 1000 or less.