KR101794526B1 - Non gloss glof ball coating paint composition, non gloss glof ball and preparing thereof - Google Patents

Abstract

The present invention relates to a matt golf ball coating paint composition. Provided are a matt golf ball coating paint composition which solves a problem in which a unique color which a cover has is not expressed as a color of the cover is scattered during injection of a golf ball and expresses a color peculiar to the cover; a matt golf ball expressing the color peculiar to the cover and having improved driving distance, rotary power and controllability; and a method for preparing a matt golf ball having excellent weather resistance, water resistance, yellowing resistance and wear resistance. The matt golf ball coating paint composition comprises a urethane modified alkyd resin as a basic resin, a hardener, a light stabilizer and a silicone-based quencher.

Description

TECHNICAL FIELD [0001] The present invention relates to a matte golf ball coating composition, a matte golf ball, and a manufacturing method thereof. BACKGROUND OF THE INVENTION 1. Field of the Invention [0002]

The present invention relates to a matte golf ball coating composition, a matte golf ball and a manufacturing method thereof, and more particularly, to a matte golf ball coating composition, The present invention relates to a matte golf ball coating composition which solves the problem that the color of the cover is not developed due to scattering of color when reflecting light and causes the cover to exhibit its own hue, And a method for manufacturing a matte golf ball having improved weatherability, water resistance, yellowing resistance and abrasion resistance.

Because various factors such as the material and the dimple design of the golf ball affect the distance, the rotation, etc., various golf balls can be manufactured according to the selected material and the dimple design.

The material of the golf ball is largely composed of natural rubber and plastic system. The core of the golf ball is made by mixing the synthetic rubber with chemicals and surrounding the center. The inner layer (hereinafter referred to as the middle layer) is made of inomer and chemical, and the outer layer (hereinafter referred to as the cover) A balloon elastomer, surlyn, urethane and the like are used, and the distance, the rotatability and the like are influenced by the material of the cover.

As a representative example of the cover, 80% or more of the two-piece ball is made of a suline material and the rest is made of a urethane material. The suline golf ball has excellent durability and rigidity, and the urethane golf ball is a soft material Which provides high back spin and low trajectory for wedge shots that require high ball control.

Generally, a golf ball is white, and it has a disadvantage that it is difficult to find a ball of a golf ball or a place where it is fallen in the case of bad weather such as rain, flow, and mist. [0004] Attempts have been made to solve the above problems, and to satisfy the demands of fashionable appearance and visibility.

As an example thereof, Korean Patent Laid-Open Publication No. 2013-0029383 discloses a polyester prepared by free radical polymerization of an unsaturated polyester prepolymer, which comprises a tint or a colorant upon coating.

In particular, the golf balls of Sullin have comparatively good compatibility with color paints, and when producing golf balls, pigments having color together with raw materials can be mixed and dispersed to form colors through injection. However, The compatibility with the coating material is low and the adhesion and abrasion resistance are poor.

Furthermore, the golf ball of a suline material or a urethane material has a problem that the color hue of the cover can not express the inherent color of the cover due to scattering during the injection of the golf ball.

SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a matte golf ball coating composition which solves the problem that the color of the cover does not express the intrinsic color of the strip as the color of the cover is scattered during injection of the golf ball, The present invention provides a matte golf ball having improved coloring, improved distance, rotation and controllability, and a method for producing a matte golf ball having excellent weather resistance, water resistance, yellowing resistance and abrasion resistance.

More particularly, the present invention relates to a matte golf ball coating composition comprising a urethane-modified alkyd resin as a base resin, a curing agent, a light stabilizer, and a silicone-based quencher, wherein the curing agent is a compound represented by the following formula (1)

[Chemical Formula 1]

Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from C ₁ -C ₃₀ linear or branched alkyl groups,

The light stabilizer is characterized by containing a C ₁ -C ₃₀ alkylene bridge having ester bonds at both ends and a C ₄ -C ₃₀ nitrogen-containing heterocyclic compound bonded to the end of the ester bond.

In addition, the present invention relates to a method for manufacturing a matte golf ball, and more particularly, A step of preparing a matte coating material; Forming a logo or mark on the pretreated golf ball; Top coating the matte coating paint; And curing the top coated golf ball,

The mat coated coating material is characterized in that the above-mentioned coating paint composition for a matte golf ball is used as a raw material.

In addition, the present invention relates to a matte golf ball, and more particularly, to a golf ball having a core which is formed by laminating one to three intermediate layers around the center and constituting an outer layer of the intermediate layer; A cover surrounding the core; And a cover surrounding the cover,

[Chemical Formula 1]

(Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from a C ₁ -C ₃₀ linear or branched alkyl group) and a curing material represented by C ₁ including; -C ₃₀ alkylene bridge, and wherein the ester containing a light-stable material and the cured product of the silicone-based quenching agent, including a heterocyclic compound containing nitrogen of C ₄ -C ₃₀ coupled to the ends of the coupling cover film .

According to the present invention, a matte-coated golf ball can solve the problem that the color of the cover does not exhibit the intrinsic hue of the band as the cover is scattered during the injection of the golf ball, the hue of the cover can be expressed, Thereby improving the stability and controllability. Particularly, the manufacturing process according to the present invention can produce a matte golf ball having excellent weather resistance, water resistance, yellowing resistance and abrasion resistance.

In addition, the matte golf ball coating composition of the present invention has an advantage that it can be applied to various golf balls such as golf balls, fluorescent dyes, and fluorescent golf balls using fluorescent pigments such as fluorescent pigments.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a photograph showing a difference in luster between a matte-coated golf ball and a conventional glossy golf ball according to the present invention. In the figure, it can be seen that the light reflection is significantly reduced in the non-glossy golf ball on the right side compared to the glossy golf ball on the left side.
2 is a view showing the distance of a matte coated golf ball according to the present invention.
3 is a view showing the rotational force of the matte-coated golf ball according to the present invention.
4 is a view showing controllability of a matte-coated golf ball according to the present invention.

Hereinafter, the present invention will be described in detail.

More particularly, the present invention relates to a matte golf ball coating composition comprising a urethane-modified alkyd resin as a base resin, a curing agent, a light stabilizer, and a silicone-based quencher, wherein the curing agent is a compound represented by the following formula (1)

[Chemical Formula 1]

Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from C ₁ -C ₃₀ linear or branched alkyl groups,

The light stabilizer may include a C ₁ -C ₃₀ alkylene bridge having ester bonds at both ends and a C ₄ -C ₃₀ nitrogen-containing heterocyclic compound bonded to the end of the ester bond.

The base resin may be a urethane-modified alkyd resin that can be used in a coating composition, and may be one prepared by condensation reaction between a linoleic oil and a compound having a urethane functional group.

The urethane-modified alkyd resin has a weight average molecular weight or a number average molecular weight of 8,000 to 12,000 g / mol, a weight average molecular weight or a number average molecular weight of 8,000 to 10,000 g / mol, a weight average molecular weight of 10,000 to 12,000 g / Molecular weight, or a weight average molecular weight or a number average molecular weight of 9,000 to 11,000 g / mol. Within this range, it is possible to provide an effect of improving interlayer adhesion with an abrasive and elastic material.

In the present description, the weight average molecular weight or the number average molecular weight can be measured using gel permeation chromatography.

The urethane-modified alkyd resin may have an OH value of 150 to 180, an OH value of 170 to 200, an OH value of 130 to 160, or an OH value of 130 to 200, and in this range, Can be improved.

In the present description, the OH value can be measured by a conventional method of measuring hydroxyl value.

The curing agent includes all of the curing agents that can be used in the coating composition, but it is preferred that R ₁ and R ₃ in formula (1) are independently selected from C ₆ -C ₃₀ linear or branched alkyl groups and R ₂ and R ₄ are each Independently, a C ₁ -C ₅ straight or branched chain alkyl group.

As a specific example, it may be a compound represented by the following formula (2).

(2)

The light stabilizer includes all the light stabilizers that can be used in the coating composition, but may specifically be a piperidinyl ester compound represented by the following formula (3).

(3)

Wherein R ₅ , R ₆ , R ₈ , R ₉ , R ₁₁ , R ₁₂ , R ₁₄ and R ₁₅ are each independently selected from C ₁ -C ₃₀ linear or branched alkyl groups and R ₇ , R ₁₃ are each independently selected from H, or straight-chain or branched alkyl group of C ₁ -C _30, R ₁₀ is a straight-chain or branched-chain of a C ₁ -C ₃₀ alkylene group),

R ₅ , R ₆ , R ₈ , R ₉ , R ₁₁ , R ₁₂ , R ₁₄ and R ₁₅ are each independently selected from C ₁ -C ₅ linear or branched alkyl groups R ₇ and R ₁₃ are H, and R ₁₀ is a compound selected from a C ₆ -C ₃₀ linear or branched alkylene group.

The light stabilizer may be, for example, a compound represented by the following general formula (4).

[Chemical Formula 4]

The silicone quencher may include any quencher that may be used in the coating composition, but may preferably be an amorphous compound having SiO ₂ as a unit.

The silicone-based light extinguishing agent is used in an amount of 3 to 15 parts by weight, 3 to 10 parts by weight, 5 to 15 parts by weight, or 4 to 10 parts by weight, based on 100 parts by weight of the photo-curing composition comprising the base resin, organic solvent, curing agent and light stabilizer of the urethane- To 10 parts by weight, and it is possible to effectively provide the light-shielding property within this range.

The photocurable composition may comprise, for example, 10 to 30% by weight of the base resin of the urethane-modified alkyd resin, 50 to 80% by weight of the organic solvent, 0.1 to 5% by weight of the curing agent, And 0.1 to 5% by weight of a stabilizer. In this range, a nitrile-based oil and NHCOO-functional group stable in a photochemical environment can be suitably provided, and can be suitably provided with water resistance, weather resistance, yellowing resistance and durability.

As another example, the photocurable composition may contain 15 to 30% by weight of the base resin of the urethane-modified alkyd resin, 60 to 75% by weight of the organic solvent, 0.1 to 5% by weight of the curing agent, And 0.1 to 5% by weight of a stabilizer. In this range, a nitrile oil and a NHCOO-functional group that are stable in a photochemical environment can be effectively used to provide water resistance, weather resistance, yellowing resistance and durability.

The photocurable composition is, for example, 20 to 35% by weight of the base resin of the urethane-modified alkyd resin, 60 to 75% by weight of the organic solvent, 0.1 to 2.5% by weight of the curing agent, And 0.1 to 2.5% by weight of a stabilizer. Within this range, it is possible to most effectively provide a water-soluble, weather-resistant, yellowing resistance and durability with a Linoleum oil and a NHCOO-functional group stable in a photochemical environment, To provide a suitable degree of dilution to provide a matte coating composition.

In addition, the organic solvent includes all solvents that can be used in the coating composition, but it is preferable to use a combination of a butyl acetate solvent and an ethyl acetate solvent so that they can be easily evaporated in a curing process.

Preferably 25 to 40% by weight of n-butyl acetate and 25 to 40% by weight of ethyl acetate solvent, more preferably 25 to 35% by weight of n-butyl acetate and 25 to 35% by weight of ethyl acetate- %. ≪ / RTI > Here, the ethyl acetate-based solvent refers to those containing 85% or more of ethyl acetate.

In the present invention, as a substitute for the curing agent or the light stabilizer, a photoinitiator generally used in the coating composition may be applied or used in combination. The photoinitiator may be an organic peroxide, an azo compound, a quinine, a nitro compound, an acyl halide, a hydrazone, a mercapto compound, a pyrylium compound, imidazole, chlorotriazine, benzoin, benzoin alkyl ether, . Commercially available photoinitiators include those sold by Ciba Geigy under the trade names Daracur ™ 1173, Darocur ™ 4265, Irgacure ™ 651, Irgacure ™ 184, Irgacure ™ 1800, 6976 and UVI-6992 from Aceto Corp. (Lake Superior, NY, USA) as Irgacure ™ 369, Irgacure ™ 1700, Irgacure ™ 907 and Irgacure ™ 819 Are included. Phenyl- [p- (2-hydroxytetradecyloxy) phenyl] iodonium hexafluoroanthomonate is a photoinitiator commercially available from Gelest (Thurlitown, Pa.). Phosphine oxide derivatives include Lucirin (TM) TPO, available from BASF (Charlotte, NC), which is 2,4,6-trimethylbenzoyldiphenylphosphine oxide. The photoinitiator may be used in an amount of about 0.1 to 10 parts by weight, or about 0.1 to 5 parts by weight based on 100 parts by weight of the matte golf ball coating composition.

As the photoinitiator, it is possible to use one having a UV absorption wavelength in the range of 50 nm or less. In particular, it is preferable to use a photoinitiator having an absorption wavelength in the range of 380 nm to 410 nm. One or more photoinitiators may be used to maximize the photocuring effect.

The additives may include at least one selected from the group consisting of heat stabilizers, UV stabilizers, and antioxidants, and various other additives may be used.

The matte golf ball coating composition according to the present invention may contain a catalyst, a leveling agent, a slip agent, a fluorescent whitening agent, a defoaming agent, a plasticizer and the like within a range satisfying the object of the invention. The matte golf ball coating composition May be used in an amount of 0.1 to 15 parts by weight based on 100 parts by weight.

The present invention also relates to a method for manufacturing a matte golf ball using the matte golf ball coating composition, and more particularly, A step S2 of producing a matte coating material; Forming a logo or mark on the preprocessed golf ball (S3); Top coating the matte coating material (S4); And curing the top coated golf ball (S5).

The golf ball used in the present invention may be a variety of golf balls such as a golf ball in a urethane cover material or a suline cover, a fluorescent golf ball using a fluorescent pigment such as a fluorescent dye, and a fluorescent pigment.

The pretreatment step S1 of the golf ball includes all treatments that facilitate the coating process such as adhesion in the subsequent coating step through the removal of foreign substances and the like. Preferably, the polished surface is polished to the inside of the dimple as in the polishing and cleaning process, and the color of the cover material can be realized.

Specifically, the preprocessing step (S1) may be a step of polishing the bottom portion of the dimple and the land portion in a cover having a plurality of dimples.

The step (S2) of producing the matte coating paint is a step of preparing the above-mentioned matte coating composition, wherein 10 to 30% by weight of the urethane-modified alkyd resin, 50 to 80% by weight of the organic solvent, 5% by weight, and 0.1 to 5% by weight of a light stabilizer; And 5 to 10 parts by weight of quenching;

The golf ball may include, for example, a cover made by a color composition containing 0.1 to 29.1 parts by weight of at least one coloring agent selected from titanium oxide, dye and pigment in 100 parts by weight of urethane resin or sulylene.

The coloring agent is, for example, 0.05 to 1.5 parts by weight of titanium oxide, 2.5 to 15.5 parts by weight of an orange coloring agent, 0.1 to 29 parts by weight of a red coloring agent, 0.01 to 10 parts by weight of a green coloring agent, 0.01 to 5 parts by weight of a blue coloring agent, 5 parts by weight of a colorant, and 0.01 to 1.5 parts by weight of a yellow colorant.

Here, the coloring agent can be variously implemented according to the combination of white, white blue, red, pink, orange, and green.

Next, step (S3) of forming a logo or mark on the preprocessed golf ball. Forming a logo or mark on the preprocessed golf ball, comprising the steps of: base coating the preprocessed golf ball; And curing the base coated golf ball.

Wherein the base coating may comprise any base coating material available in the art. The base coating material may be applied as well as a single coating as well as a plurality of repeated coatings if necessary.

The base coating can be formed by inkjet printing, slit coating, spin coating, spray coating or the like, and is not limited to the proposed method.

It is possible to visually and clearly provide the logo or mark through the preprocessing such as the above-mentioned polishing.

Next, top coating (S4) of the matte coating material is performed. At this time, the top coating paint may be repeatedly coated a plurality of times as necessary, but since the gloss of the cover surface is blocked through a pretreatment such as the above-mentioned polishing, a matt coating effect can be sufficiently provided even by a single coating.

The weight of the matte coating material applied once in the top coating step is not limited thereto, but may be, for example, 100 to 300 mg.

The thickness of the top coat layer may be, for example, 10 to 30 占 퐉, and preferably 15 to 30 占 퐉 thick. When the thickness of the thin film is less than 10 mu m, the photo-curing reaction progresses rapidly but the cover film characteristics are deteriorated. If the thickness exceeds 30 mu m, the photocuring reaction is slow, so that sufficient hardening of the cover coat is difficult to occur.

Next, step (S5) of curing the top coated golf ball may be included. However, it is preferable to thermoset at 50 to 70 DEG C for 10 to 20 minutes in the curing efficiency, and then photo-cure by UV, NIR (Near Infrared) or the like.

The core, cover and top coating may be applied by application and drying, where application may be by dry or wet process. In the case of a dry process, for example, it can be carried out under high vacuum in a thermal and / or vapor deposition process. In the case of a wet process, the resin or its solution is applied by various processes such as spin coating, slit coating, spray coating, inkjet printing, gravure printing, comma coating, or roll-to-roll process under a normal pressure and a nitrogen atmosphere . After application, it can be photo-cured by irradiating UV, for example.

In addition, the present invention relates to a matte golf ball provided by matte coating on a golf ball using the matte golf ball coating composition, wherein one to three intermediate layers are laminated around the center, A core constituting the core;

A cover surrounding the core; And a cover surrounding the cover,

[Chemical Formula 1]

(Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from a C ₁ -C ₃₀ linear or branched alkyl group) and a curing material represented by C ₁ including; -C ₃₀ alkylene bridge, and wherein the ester containing a light-stable material and the cured product of the silicone-based quenching agent, including a heterocyclic compound containing nitrogen of C ₄ -C ₃₀ coupled to the ends of the coupling cover film .

The intermediate layer has a thickness of, for example, 0.9 to 2 mm, and the core has a thickness of, for example, 30 to 40.5 mm, and the cover may have a thickness of 1.0 to 2.4 mm, for example.

The cover coat may have a gloss measured by a gloss measuring device with a tilt of 45 degrees, for example, within a range of 0 to 30, 0 to 10, 0 to 5, or 0 to 2, and within this range, It is possible to effectively provide a matte effect.

In this specification, a gloss measuring device with a 45 degree slope may be measured in accordance with ASTM D528 using a gloss meter at an angle of 45 degrees.

The chromaticity of the cover coating film measured by the CIELAB colorimetric system can satisfy, for example, the following formula 1, and can effectively provide the yellowing resistance and the desired matting effect within this range.

[Formula 1]

50 <L * <90, -40 <a * <- 35 or 50 <a * <75, 25 <b * <35 or 70 <b * <110

The core may include all of the cores available in the art, but if it contains 0.5 to 2.5 parts by weight of titanium oxide per 100 parts by weight of the butadiene rubber resin, it will block ultraviolet rays to provide an advantage of preventing oxidation of the core .

The core may be transparent or translucent or opaque.

The intermediate layer may include all the intermediate layers usable in the related art. However, in the case where 0.2 to 4.5 parts by weight of titanium oxide is contained in 100 parts by weight of an ionomer, for example, HPF material of Dupont Co., It is possible to provide an advantage of preventing the oxidation of the catalyst.

The intermediate layer may be transparent or translucent or opaque.

The cover may include all the covers available in the art, but it may be manufactured by a color composition containing 0.1 to 29.1 parts by weight of at least one colorant selected from titanium oxide, dye and pigment in 100 parts by weight of urethane resin or sulphine Is preferable because it can provide the advantage of expressing the inherent color and ultraviolet shielding.

The cover may be transparent or translucent or opaque.

Wherein the coloring agent comprises 0.05 to 1.5 parts by weight of titanium oxide, 2.5 to 15.5 parts by weight of an orange coloring agent, 0.1 to 29 parts by weight of a red coloring agent, 0.01 to 10 parts by weight of a green coloring agent, 0.01 to 5 parts by weight of a blue coloring agent, , And 0.01 to 1.5 parts by weight of a yellow colorant.

The cover preferably has a plurality of dimples and has a thickness of approximately 10 to 30 microns uniform in the dimple bottom portion and the land portion, and has a dimple at a corresponding position of the dimple of the cover of the core surface.

The thickness of the cover is, for example, 1.0 mm to 2.4 mm, or 1.2 mm to 2.2 mm. If the thickness is less than the above-mentioned thickness, it is not suitable to form a dimple for forming a constant cover thickness. If it exceeds the above-mentioned thickness, the process cost is increased and the permeability is decreased.

It is preferable that the chromaticity of the golf ball is a color difference ( DELTA E) between the intermediate layer and the cover in the CIELAB colorimetric system is 12 or less.

The color of a golf ball is the color difference (△ E) of the intermediate layer and the cover 12 or less in the CIELAB color system, it is more preferable that the color difference (△ E) of the core and the cover 12 or less.

The color of a golf ball is the color difference (△ E) of the intermediate layer and the cover 12 or less in the CIELAB color system, it is still more preferred that the color difference (△ E) of the intermediate layer and the core 12 or less.

The color of a golf ball is the color difference (△ E) of the intermediate layer and the cover 12 or less in the CIELAB color system, an intermediate layer and a is less than or equal to 12, the color difference (△ E) of the core, the core and the color difference (△ E) of the cover Most preferably 12 or less.

In the present invention, a spectrophotometer capable of color analysis can be used for the measurement of the CIELAB colorimetric system.

As described above, the golf ball according to the present invention employs a cover coating which prevents scattering of color during injection and ensures the color luster of the resin itself, so that not only visibility and matting effect are excellent, but also weather resistance, water resistance, And excellent abrasion resistance.

Hereinafter, the present invention will be described with reference to preferred embodiments and comparative examples. However, the following examples are presented for convenience of explanation only to assist the description of the present invention, and the present invention is not limited to the following examples.

[Example]

&Lt; Example 1-4 >

As the golf ball to be used in the embodiment, the core contains titanium oxide in an amount of 0.5 to 2.5 parts by weight based on 100 parts by weight of butadiene rubber resin, and is mixed and vulcanized to have a size of 30 to 40.50 mm.

The intermediate layer of the golf ball contained 0.2 to 4.5 parts by weight of titanium oxide per 100 parts by weight of HPF material manufactured by Dupont Co., and was injected into a center and dried to form two layers of 0.9 to 2.0 mm in thickness.

The cover is coated and dried on the core by a color composition containing 0.1 to 29.1 parts by weight of at least one coloring agent selected from the group consisting of urethane resin or selenium, and at least one colorant selected from titanium oxide, dye and pigment, To prepare a transparent layer. Herein, six kinds of golf balls having different colors were prepared using the prescription of Table 1 below.

Color Recipe Pink Surlyn or Urethane TiO ₂ ORANGE RED 100 parts 0.34 parts 4.3 parts 0.9 parts Red Surlyn or Urethane RED ORANGE 100 parts 16 parts 10.1 parts Orange Surlyn or Urethane orange green TiO ₂ 100 parts 6 parts 0.88 parts 0.2 parts Blue Surlyn or Urethane blue 100 parts 0.1 parts Yellow Surlyn or Urethane TiO ₂ green yellow 100 parts 0.2 parts 0.01 parts 0.56 parts White Surlyn or Urethane TiO ₂ Ultra Blue 100 parts 3 parts 0.2 parts

The cover has a plurality of dimples and has a film thickness of approximately 10 to 30 microns uniform in the dimple bottom and land portions and has a dimple at a corresponding position of the dimple of the cover of the core surface.

Pretreatment of golf balls (S1)

In step S1, the surface gloss of the prepared golf ball cover was subjected to a quenching treatment through a polishing process as a pretreatment step for the bottom portion of the dimple and the land portion.

Preparation of matte coating (S2)

In step S2, 10 to 30% by weight of a urethane-modified alkyd resin (number average molecular weight: 8,000 to 12,000 g / mol, OH value: 150 to 180) relative to the total weight of the matte golf ball coating composition was mixed with normal butyl acetate 25 To 25% by weight of an ethyl acetate solvent (containing 85% ethyl acetate), 0.1 to 5% by weight of a compound of the formula (2) as a curing agent of the formula (1) 5% by weight of a photo-curing composition, and 5 to 10 parts by weight of an amorphous silicon oxide as a quencher were mixed to prepare a matte coating paint.

(2)

 [Chemical Formula 4]

Form a logo or mark on a golf ball (S3)

Spray coating a base coating paint on the pre-treated golf ball and curing the base coated golf ball as step S3.

Here, the base coating was spray coated using a base coating paint containing a urethane resin, which is commonly used, and then cured under NIR (near-infrared) conditions or thermal drying.

The logo or mark was then provided visually and clearly.

Top coating of matte coating (S4)

Next, the matte coating paint was top coated. The weight of the matte coating paint applied once was 100 to 300 mg, and the thickness of the top coating layer was adjusted to have a thickness of 15 to 30 탆.

Curing of top coated golf balls (S5)

Next, the top coated golf ball was cured. The curing was carried out at 50-7O &lt; 0 &gt; C for 10-20 minutes and then under NIR (Near Infrared) drying conditions.

<Performance test>

Performance was tested in the following manner.

Glossiness: The golf ball was visually observed under the fluorescent light to observe the difference of the light reflection, and prepared against Fig. 1, it can be seen that the light reflection is significantly reduced in the right-hand non-glossy golf ball compared to the left-hand glossy golf ball.

Adhesiveness: The logo of the golf ball was cut out at a distance of 1 mm (horizontal and vertical) using a Doruko knife having an area of 15 to 20 mm in width and then peeled off when the transparent tape was pulled three times in the vertical direction. The state in which the paint is not peeled is denoted as O, the state in which one or two sections are peeled off is indicated by △, and the state in which three or more sections are peeled off is indicated as NG.

Abrasion Resistance : The golf ball was placed in a SUS container containing grindstone and water, and after 6 hours of rotation, the paint abrasion on the golf ball surface was visually observed and evaluated repeatedly four times and the average was calculated. When the surface state is almost indistinguishable from the initial and visual states, it is expressed as 5 (excellent), and when the peeled portion of the paint is visually distinguished, it is indicated as 1 (poor).

Field test: The golf ball was hit 100 times continuously at a speed of 40 m / sec, and the paint adhesion was visually observed three times. The state in which no paint peeling off of the ball is indicated as O, the state where paint peeling of 1 or 2 of the whole of the ball is occurred is indicated as △, and when three or more peeling of the whole of the ball occurs, the state is indicated as NG.

The results of the above test were summarized in Table 2 below.

color type Adhesion Abrasion resistance test Field test 1 time Episode 2 3rd time 1 time Episode 2 3rd time 4 times Average 1 time Episode 2 3rd time Red Matte O O O 4 4 4 4.5 4.1 O O O Pink Matte O O O 4 4 4 4 4.0 O O O Orange Matte O O O 4.5 4.5 4.5 4.5 4.5 O O O Yellow Matte O O O 4 4.5 4.5 4 4.25 O O O Red Bright O △ O 4 4 4 4 4.0 O O O Pink Bright O O △ 4 4 4 4 4.0 O O O Orange Bright O O △ 4 4 4 4 4.0 O O O Yellow Bright △ O O 4 4 4 4 4.0 O O O

For reference, in Table 2, glossiness is obtained by using a conventional glossy coating composition (for example, a coating composition used in NIKKA's glossy color series of NIKKO Co., Ltd.) in place of the matte coating composition according to the present invention, Can be utilized.

As shown in Table 2, the matte golf balls prepared using the matte golf ball coating composition of the present invention are superior in adhesion, abrasion resistance, and field test compared to conventional golf ball or matte color series of Volvik It was confirmed that it shows excellent performance in all parts.

The colorless CIELAB test and the HUNTER LAB test were performed on the above-mentioned matte golf balls, respectively, and the results of the chromaticity and yellowing index are summarized in Table 3 below:

BALL NO. AVERAGE CIELAB AVERAGE HUNTER L * a * b * L a b YI RED 55.17 71.7 34.79 48.06 73.84 21.27 189.08 ORANGE 73.27 52.23 72.02 67.51 54.95 40.14 164.56 YELLOW 88.85 -38.49 90 85.93 -35.23 52.53 80.02 PINK 61.91 67.26 27.16 55.04 70.26 18.96 152.97 VOLVIK RED 50.16 73.44 41.76 43.08 74.53 22.47 217.09 VOLVIK ORANGE 78.58 54.84 89.86 73.62 59.32 46.87 171.51 VOLVIK YELLOW 91.24 -43.88 104.87 88.89 -40.22 57.18 82.68 VOLVIK PINK 70.58 83.8 23.58 64.48 93.82 18.18 154.58

As can be seen from Table 3 above, improved results are obtained for both chromaticity and yellowing index.

Further, the distance of the matte coated golf ball according to the present invention and the commercially available product was measured and shown in FIG. A commercially available product of NIKE Corporation's glossy color series (referred to as "third party A") and a ballistic colorless series (referred to as third party B). As shown in Fig. 2, an improved spin rate was confirmed with respect to a commercially available product.

In addition, the rotational force of the matte coated golf ball according to the present invention and the commercially available product was measured and shown in FIG. A commercially available product of NIKE Corporation's glossy color series (referred to as "third party A") and a ballistic colorless series (referred to as third party B). As shown in FIG. 3, the improved distance compared to the commercial product was confirmed.

Further, the controllability of a matte coated golf ball according to the present invention and a commercially available product was measured and shown in FIG. A commercially available product of NIKE Corporation's glossy color series (referred to as "third party A") and a ballistic colorless series (referred to as third party B). As shown in Fig. 4, control results similar to those of the commercial products were confirmed.

Claims (17)

A curing agent, a light stabilizer, and a silicone-based light extinguishing agent, wherein the curing agent is a compound represented by the following formula (1)
[Chemical Formula 1]

Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from C ₁ -C ₃₀ linear or branched alkyl groups,
Wherein the light stabilizer comprises a C ₁ -C ₃₀ alkylene bridge having ester bonds at both ends and a C ₄ -C ₃₀ nitrogen containing heterocyclic compound bonded to the end of the ester bond, (2). The method according to claim 1,
Wherein the base resin has a number average molecular weight of 8,000-12,000 g / mol and an OH value of 150-180. The method according to claim 1,
Wherein the curing agent is from a straight-chain or branched-chain alkyl group of formula I R _1, R ₃ are independently selected from straight chain or branched alkyl group of _{C 6 -C 30, R 2,} R 4 are each independently C ₁ -C ₅ &Lt; / RTI &gt; is a selected compound. The method according to claim 1,
Wherein the light stabilizer is a piperidinyl ester compound represented by the following general formula (3): &lt; EMI ID =
(3)

Wherein R ₅ , R ₆ , R ₈ , R ₉ , R ₁₁ , R ₁₂ , R ₁₄ and R ₁₅ are each independently selected from C ₁ -C ₃₀ linear or branched alkyl groups and R ₇ , R ₁₃ are each independently selected from H, or straight-chain or branched alkyl group of C ₁ -C _30, R ₁₀ is a straight-chain or branched-chain of a C ₁ -C ₃₀ alkylene group), 5. The method of claim 4,
The light stabilizer has the formula 3 in _{R 5, R 6, R 8} , R 9, R 11, R 12, R 14, R 15 are each independently selected from straight chain or branched alkyl group of C ₁ -C _5, R ₇ and R ₁₃ are H and R ₁₀ is a compound selected from C ₆ -C ₃₀ linear or branched alkylene groups. The method according to claim 1,
Wherein the silicone-based quencher is an amorphous compound having an SiO ₂ unit. The method according to claim 1,
Wherein the silicone-based quencher is 3 to 15 parts by weight based on 100 parts by weight of the photocurable composition comprising the base resin, organic solvent, curing agent and light stabilizer of the urethane-modified alkyd resin. 8. The method of claim 7,
The photo-curable composition comprises 10 to 30% by weight of the base resin, 50 to 80% by weight of the organic solvent, 0.1 to 5% by weight of the curing agent, and 0.1 to 5% by weight of the light stabilizer, based on the total weight of the photo- By weight based on the total weight of the coating composition. A pre-processing step of a golf ball;
A step of preparing a matte coating material;
Forming a logo or mark on the pretreated golf ball;
Top coating the matte coating paint; And
And curing the top coated golf ball,
The matte coating composition is a coating composition comprising 10 to 30% by weight of a urethane-modified alkyd resin, 50 to 80% by weight of an organic solvent, 0.1 to 5% by weight of a curing agent and 0.1 to 5% by weight of a light stabilizer based on the total weight of the coating composition 100 parts by weight of a composition and 3 to 15 parts by weight of a quencher, wherein the curing agent is a compound represented by the following formula (1), wherein the light stabilizer is a C ₁ -C ₃₀ alkylene bridge having ester bonds at both ends thereof, And a C ₄ -C ₃₀ nitrogen-containing heterocyclic compound bonded to the end of the ester bond.
[Chemical Formula 1]

Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from C ₁ -C ₃₀ linear or branched alkyl groups,
10. The method of claim 9,
Wherein the preprocessing step of the golf ball is performed on a cover having a plurality of dimples, wherein the bottom portion and the land portion of the dimple are polished. 11. The method of claim 10,
The cover is an outer layer surrounding the core. The cover is composed of 100 parts by weight of urethane resin or sulphine and 0.05 to 1.5 parts by weight of titanium oxide, 2.5 to 15.5 parts by weight of orange color, 0.1 to 29 parts by weight of red color, 0.01 to 10 parts by weight of green color, 0.01 to 5 parts by weight of a blue colorant, 0.01 to 5 parts by weight of an ultra-blue coloring agent, and 0.01 to 1.5 parts by weight of a yellow coloring agent, and 0.1 to 29.1 parts by weight of a coloring agent which is transparent or opaque or translucent Wherein the golf ball is a golf ball. 12. The method of claim 11,
Wherein the core is an outer layer surrounding an intermediate layer surrounding the center of the golf ball, wherein the core is provided in a composition of 100 parts by weight of butadiene rubber resin and 0.5 to 2.5 parts by weight of titanium oxide. 13. The method of claim 12,
Wherein the intermediate layer is provided in a composition of 100 parts by weight of an ionomer resin and 0.2 to 4.5 parts by weight of titanium oxide and has a laminated structure of 1 to 3 layers and is transparent, translucent or opaque. . 10. The method of claim 9,
Forming a logo or mark on the pretreated golf ball,
Wherein the pretreatment is performed after the base coat is applied to the pretreated golf ball. A core constituting an outer layer of the intermediate layer and being laminated with a middle layer of one to three layers surrounding the center; A cover surrounding the core; And a urethane-modified alkyd resin surrounding the cover,

[Chemical Formula 1]

(Wherein R ₁ , R ₂ , R ₃ and R ₄ are each independently selected from a C ₁ -C ₃₀ linear or branched alkyl group) and a curing material represented by C ₁ including; -C ₃₀ alkylene bridge, and wherein the ester containing a light-stable material and the cured product of the silicone-based quenching agent, including a heterocyclic compound containing nitrogen of C ₄ -C ₃₀ coupled to the ends of the coupling cover film Wherein the golf ball is a golf ball. 16. The method of claim 15,
Wherein the intermediate layer has a thickness of 0.9 mm to 2.0 mm, the core has a thickness of 30 mm to 40.50 mm, and the cover has a thickness of 1.0 to 2.4 mm. 16. The method of claim 15,
Characterized in that the cover has a plurality of dimples and each of the bottom portion and the land portion constituting the dimple has a thickness of 10 to 30 占 퐉 and the dimple is provided on the core surface at a position corresponding to the dimple of the cover Matte golf ball.

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