KR102156097B1 - A paint composition with fast drying rate - Google Patents

A paint composition with fast drying rate Download PDF

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KR102156097B1
KR102156097B1 KR1020200081211A KR20200081211A KR102156097B1 KR 102156097 B1 KR102156097 B1 KR 102156097B1 KR 1020200081211 A KR1020200081211 A KR 1020200081211A KR 20200081211 A KR20200081211 A KR 20200081211A KR 102156097 B1 KR102156097 B1 KR 102156097B1
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weight
parts
acid
acrylic resin
resistance
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길승범
김종현
김명진
박문수
길유성
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삼지산물(주)
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/06Ethers; Acetals; Ketals; Ortho-esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • C08K2003/265Calcium, strontium or barium carbonate

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

The present invention relates to a paint composition having fast drying speed, low yellowing, and excellent abrasion resistance, adhesion, thermal stability, impact resistance and water resistance and, more specifically, to a paint composition comprising: an acrylic resin; titanium dioxide; calcium carbonate; a dispersant; hollow polystyrene particles; and a crack inhibitor. The paint composition has fast drying speed, low yellowing, and excellent abrasion resistance, adhesion, thermal stability, impact resistance, and water resistance. In addition, the paint composition is capable of improving abrasion resistance and retroreflective luminance by increasing adhesion power to asphalt, ascon, and glass beads.

Description

건조속도가 향상된 도료 조성물{A paint composition with fast drying rate}Coating composition with improved drying speed {A paint composition with fast drying rate}

본 발명은 건조속도가 빠르고, 황변도가 낮으며, 내마모성, 접착성, 열안정성, 내충격성 및 내수성이 우수한 도료 조성물에 관한 것으로, 더욱 상세하게는 아크릴 수지; 이산화티탄; 탄산칼슘; 분산제; 폴리스티렌 중공입자; 및 크랙방지제를 포함하는 도료 조성물에 관한 것이다.The present invention relates to a coating composition having high drying speed, low yellowing, and excellent abrasion resistance, adhesiveness, thermal stability, impact resistance and water resistance, and more particularly, acrylic resin; Titanium dioxide; Calcium carbonate; Dispersant; Hollow polystyrene particles; And it relates to a coating composition comprising a crack inhibitor.

도료로부터 제조된 도막은 자외선이나 열에 장기간 노출되면 도막을 구성하는 고분자 사슬이 분쇄되어 도막의 특성이 저하될 뿐 아니라 분쇄 시 다양한 오염물질의 발생으로 환경문제를 유발할 수 있다. When a coating film made from a paint is exposed to ultraviolet rays or heat for a long period of time, the polymer chains constituting the coating film are crushed to deteriorate the characteristics of the coating film, and various contaminants may be generated during pulverization, causing environmental problems.

한편 환경에 대한 규제가 강화되면서 도료, 코팅제 및 접착제 분야에서도 휘발성 유기 화합물의 방출에 대한 규제가 엄격해지고 있다.Meanwhile, as environmental regulations are strengthened, regulations on the release of volatile organic compounds are becoming stricter in the fields of paints, coatings and adhesives.

따라서 자외선이나 열에 장기간 노출되더라도 도막의 특성이 유지되고 휘발성 유기 화합물의 함량이 적은 수용성 도료에 대한 수요가 급증하고 있다. Therefore, even when exposed to ultraviolet rays or heat for a long period of time, the demand for water-soluble paints having a low content of volatile organic compounds and maintaining the properties of the coating film is increasing rapidly.

그러나 수용성 도료는 건조속도가 용제형 도료에 비하여 느려서 시공시간이 오래 걸리는 단점이 있으며, 내수성과 내마모성이 저하되어 신뢰성 측면에서 치명적인 단점이 있다. However, water-soluble paints have a disadvantage in that the drying speed is slower than that of solvent-type paints, so it takes a long time to construct, and there is a fatal disadvantage in terms of reliability due to deterioration of water resistance and abrasion resistance.

이와 관련하여 한국등록특허 제10-1558876호는 아크릴레이트 또는 메타아크릴레이트 반복단위를 포함하며, 경화제에 의해 가교화된 아크릴 수지, 유색안료 및 체질안료를 포함하는 수용성 노면 표지용 도료 조성물을 개시하고 있다. In this regard, Korean Patent Registration No. 10-1558876 discloses a water-soluble road surface coating composition comprising an acrylate or methacrylate repeating unit and comprising an acrylic resin, a colored pigment, and an extender pigment crosslinked by a curing agent. have.

그러나 상기 문헌에 개시된 도료 조성물은 건조속도가 느리고, 황변도, 내마모성, 접착성, 열안정성, 내충격성 및 내수성이 여전히 불량하다. However, the coating composition disclosed in the above document has a slow drying speed, and still has poor yellowness, abrasion resistance, adhesion, thermal stability, impact resistance, and water resistance.

한국등록특허 제10-1558876호(2015.10.02.)Korean Patent Registration No. 10-1558876 (2015.10.02.)

본 발명은 상기 종래 기술의 문제점을 해결하기 위한 것으로서, 건조속도가 빠르고, 황변도가 낮으며, 내마모성, 접착성, 열안정성, 내충격성 및 내수성이 우수한 도료 조성물을 제공하는데 그 목적이 있다. An object of the present invention is to provide a coating composition having a high drying speed, low yellowing, abrasion resistance, adhesion, thermal stability, impact resistance and water resistance, as to solve the problems of the prior art.

또한 본 발명은 아스팔트, 아스콘 및 글래스 비드와의 접착력을 증가시켜 내마모도와 재귀반사휘도를 향상시킬 수 있는 도료 조성물을 제공하는 것을 목적으로 한다. Another object of the present invention is to provide a coating composition capable of improving wear resistance and retroreflective luminance by increasing adhesion to asphalt, ascon, and glass beads.

상기와 같은 목적을 달성하기 위하여 본 발명은 아크릴 수지; 이산화티탄; 탄산칼슘; 분산제; 폴리스티렌 중공입자; 및 크랙방지제를 포함하는 도료 조성물을 제공한다.In order to achieve the above object, the present invention is an acrylic resin; Titanium dioxide; Calcium carbonate; Dispersant; Hollow polystyrene particles; And it provides a coating composition comprising a crack inhibitor.

본 발명의 일실시예에 있어서, 상기 아크릴 수지 100중량부에 대하여 이산화티탄 3~100중량부, 탄산칼슘 50~300중량부, 분산제 0.1~5중량부, 폴리스티렌 중공입자 0.5~30중량부 및 크랙방지제 2~20중량부를 포함하는 것을 특징으로 한다.In an embodiment of the present invention, based on 100 parts by weight of the acrylic resin, 3 to 100 parts by weight of titanium dioxide, 50 to 300 parts by weight of calcium carbonate, 0.1 to 5 parts by weight of dispersant, 0.5 to 30 parts by weight of hollow polystyrene particles, and cracks It characterized in that it contains 2 to 20 parts by weight of the inhibitor.

본 발명의 일실시예에 있어서, 상기 아크릴 수지 100중량부에 대하여 아크릴레이트기 함유 실란 커플링제 및 아크릴산 모노머의 공중합체 1~10중량부를 추가로 포함하는 것을 특징으로 한다.In one embodiment of the present invention, it is characterized in that it further comprises 1 to 10 parts by weight of a copolymer of an acrylate group-containing silane coupling agent and an acrylic acid monomer based on 100 parts by weight of the acrylic resin.

본 발명의 일실시예에 있어서, 상기 크랙방지제는 트리프로필렌글리콜 n-부틸에테르 또는 디프로필렌글리콜 n-부틸에테르인 것을 특징으로 한다.In one embodiment of the present invention, the crack inhibitor is characterized in that tripropylene glycol n-butyl ether or dipropylene glycol n-butyl ether.

또한 본 발명은 상기 도료 조성물을 포함하는 제품에 있어서, 상기 제품은 도료, 코팅제 또는 접착제인 것을 특징으로 한다. In addition, the present invention is characterized in that in the product comprising the coating composition, the product is a paint, a coating agent or an adhesive.

본 발명은 건조속도가 빠르고, 황변도가 낮으며, 내마모성, 접착성, 열안정성, 내충격성 및 내수성이 우수한 도료 조성물을 제공할 수 있다. The present invention can provide a coating composition having high drying speed, low yellowing, and excellent abrasion resistance, adhesiveness, thermal stability, impact resistance, and water resistance.

또한 본 발명은 아스팔트, 아스콘 및 글래스 비드와의 접착력을 증가시켜 내마모도와 재귀반사휘도를 향상시킬 수 있는 도료 조성물을 제공할 수 있다.In addition, the present invention can provide a coating composition capable of improving abrasion resistance and retroreflective luminance by increasing adhesion with asphalt, ascon, and glass beads.

이하 실시예를 바탕으로 본 발명을 상세히 설명한다. 본 발명에 사용된 용어, 실시예 등은 본 발명을 보다 구체적으로 설명하고 통상의 기술자의 이해를 돕기 위하여 예시된 것에 불과할 뿐이며, 본 발명의 권리범위 등이 이에 한정되어 해석되어서는 안 된다.The present invention will be described in detail based on the following examples. The terms, examples, etc. used in the present invention are merely exemplified to describe the present invention in more detail and to aid understanding of those skilled in the art, and the scope of the present invention should not be interpreted as being limited thereto.

본 발명에 사용되는 기술 용어 및 과학 용어는 다른 정의가 없다면 이 발명이 속하는 기술 분야에서 통상의 지식을 가진 자가 통상적으로 이해하고 있는 의미를 나타낸다.Technical terms and scientific terms used in the present invention represent the meanings commonly understood by those of ordinary skill in the art, unless otherwise defined.

본 발명은 아크릴 수지; 이산화티탄; 탄산칼슘; 분산제; 폴리스티렌 중공입자; 및 크랙방지제를 포함하는 도료 조성물에 관한 것이다. The present invention is an acrylic resin; Titanium dioxide; Calcium carbonate; Dispersant; Hollow polystyrene particles; And it relates to a coating composition comprising a crack inhibitor.

상기 도료 조성물은 아크릴 수지 100중량부에 대하여 이산화티탄 3~100중량부, 탄산칼슘 50~300중량부, 분산제 0.1~5중량부, 폴리스티렌 중공입자 0.5~30중량부 및 크랙방지제 2~20중량부를 포함할 수 있다. The coating composition includes 3 to 100 parts by weight of titanium dioxide, 50 to 300 parts by weight of calcium carbonate, 0.1 to 5 parts by weight of dispersant, 0.5 to 30 parts by weight of polystyrene hollow particles, and 2 to 20 parts by weight of crack inhibitor based on 100 parts by weight of acrylic resin. Can include.

상기 아크릴 수지는 도막의 표면 경도를 높여주고 기재에 대한 접착성, 내마모성, 내충격성, 내수성 및 내후성을 부여하는 작용을 한다. The acrylic resin functions to increase the surface hardness of the coating film and to impart adhesion to the substrate, abrasion resistance, impact resistance, water resistance and weather resistance.

아크릴 수지는 분자 내에 아크릴기를 갖는 고분자라면 특별히 제한이 없으며, 아크릴계 모노머를 중합하여 제조되거나 아크릴계 모노머와 다른 모노머를 공중합하여 제조될 수 있다. The acrylic resin is not particularly limited as long as it is a polymer having an acrylic group in the molecule, and may be prepared by polymerizing an acrylic monomer or copolymerizing an acrylic monomer with another monomer.

또한 아크릴 수지는 고형의 아크릴 수지이거나 또는 아크릴 수지 에멀젼이 사용될 수 있으며, 이때 아크릴 수지 에멀젼에 포함된 고형분의 함량은 20~60중량%인 것이 바람직하다. In addition, the acrylic resin may be a solid acrylic resin or an acrylic resin emulsion may be used, and in this case, the content of the solid content contained in the acrylic resin emulsion is preferably 20 to 60% by weight.

상기 아크릴 수지는 유화중합으로 중합될 수 있으며, 음이온이 부여된 음이온성 아크릴 수지일 수도 있다. 상기 음이온성 아크릴 수지를 제조하기 위해서는, 아크릴 수지의 유화중합 동안에 음이온성 계면활성제나 음이온성 분산제를 첨가하거나 또는 아크릴 수지의 유화중합 후에 음이온성 계면활성제나 음이온성 분산제를 첨가할 수 있다. The acrylic resin may be polymerized by emulsion polymerization, and may be an anionic acrylic resin to which anion is imparted. In order to prepare the anionic acrylic resin, an anionic surfactant or an anionic dispersant may be added during emulsion polymerization of the acrylic resin, or an anionic surfactant or anionic dispersant may be added after emulsion polymerization of the acrylic resin.

상기 음이온성 계면활성제 또는 음이온성 분산제로는 황산염; 술폰산염; 인산염; 지방산 로신 및 나프텐산의 염; 나프탈렌 설폰산 및 저분자량의 포름알데히드의 농축 생성물; 소디움 라우릴 설페이트와 같은 금속 알킬 설페이트; 도데실벤젠 설폰산, 이소프로필벤젠 설폰산 등의 염; 이소프로필나프탈렌 설폰산과 같은 알킬 아릴 설폰산의 염; 디옥틸설포석신산, 설포석신산, 옥틸 설포석신산, N-메틸-N-팔미토일 타우르산, 올레일이스에티온산 등과 같은 알킬 석포석신산의 염; t-옥틸페녹시-폴리에톡시에틸 황산 나트륨과 같은 알킬아릴폴리에톡시에틸 황산의 금속염 등이 사용될 수 있다. As the anionic surfactant or anionic dispersant, a sulfate; Sulfonate; phosphate; Salts of fatty acids rosine and naphthenic acid; Concentrated product of naphthalene sulfonic acid and low molecular weight formaldehyde; Metal alkyl sulfates such as sodium lauryl sulfate; Salts such as dodecylbenzene sulfonic acid and isopropylbenzene sulfonic acid; Salts of alkyl aryl sulfonic acids such as isopropylnaphthalene sulfonic acid; Salts of alkyl sulfosuccinic acid such as dioctyl sulfosuccinic acid, sulfosuccinic acid, octyl sulfosuccinic acid, N-methyl-N-palmitoyl tauric acid, and oleyl ethionic acid; Metal salts of alkylarylpolyethoxyethyl sulfuric acid such as sodium t-octylphenoxy-polyethoxyethyl sulfate, and the like may be used.

상기 아크릴 수지의 제조에 사용되는 아크릴계 모노머는 메틸아크릴레이트, 에틸아크릴레이트, 프로필아크릴레이트, 이소프로필아크릴레이트, n-부틸아크릴레이트, 이소부틸아크릴레이트, n-아밀아크릴레이트, 이소아밀아크릴레이트, n-헥실아크릴레이트, 2-에틸헥실아크릴레이트, 히드록시메틸아크릴레이트, 2-히드록시에틸아크릴레이트, 히드록시프로필아크릴레이트, 라우릴아크릴레이트, 메틸메타크릴레이트, 에틸메타크릴레이트, 프로필메타크릴레이트, 이소프로필메타크릴레이트, n-부틸메타크릴레이트, 이소부틸메타크릴레이트, n-아밀메타크릴레이트, 이소아밀메타크릴레이트, n-헥실메타크릴레이트, 2-에틸헥실메타크릴레이트, 히드록시메틸메타크릴레이트, 히드록시프로필메타크릴레이트, 라우릴메타크릴레이트, 아크릴산, 메타크릴산, 메틸 아크릴산, 에틸 아크릴산, 부틸 아크릴산, 2-에틸 헥실 아크릴산, 데실아크릴산, 메틸 메타크릴산, 에틸 메타크릴산, 부틸 메타크릴산, 2-에틸 헥실 메타크릴산, 데실메타크릴산 등이 있다. Acrylic monomers used in the preparation of the acrylic resin are methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, n-amyl acrylate, isoamyl acrylate, n-hexyl acrylate, 2-ethylhexyl acrylate, hydroxymethyl acrylate, 2-hydroxyethyl acrylate, hydroxypropyl acrylate, lauryl acrylate, methyl methacrylate, ethyl methacrylate, propyl meth Acrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, n-amyl methacrylate, isoamyl methacrylate, n-hexyl methacrylate, 2-ethylhexyl methacrylate, Hydroxymethylmethacrylate, hydroxypropylmethacrylate, lauryl methacrylate, acrylic acid, methacrylic acid, methyl acrylic acid, ethyl acrylic acid, butyl acrylic acid, 2-ethyl hexyl acrylic acid, decylacrylic acid, methyl methacrylic acid, ethyl Methacrylic acid, butyl methacrylic acid, 2-ethyl hexyl methacrylic acid, decyl methacrylic acid, and the like.

상기 이산화티탄은 백색도 및 내마모성을 향상시키기 위하여 사용될 수 있다.The titanium dioxide may be used to improve whiteness and abrasion resistance.

상기 이산화티탄의 함량은 아크릴 수지 100중량부에 대하여 3~100중량부인 것이 바람직하며, 함량이 3중량부 미만인 경우 백색도 및 내마모성이 저하되고, 100중량부를 초과하는 경우 도막의 내충격성이 오히려 저하되며 가격이 많이 상승된다.The content of the titanium dioxide is preferably 3 to 100 parts by weight based on 100 parts by weight of the acrylic resin, and if the content is less than 3 parts by weight, whiteness and abrasion resistance decrease, and if it exceeds 100 parts by weight, the impact resistance of the coating film is rather reduced. The price rises a lot.

상기 이산화티탄은 아크릴레이트기 함유 실란 커플링제로 표면 처리될 수 있다.The titanium dioxide may be surface-treated with an acrylate group-containing silane coupling agent.

상기 이산화티탄의 표면에 도입된 아크릴레이트기는 아크릴 수지와의 접착 특성을 개선하여 조성물의 내구성, 내수성 및 내마모성을 향상시킬 수 있다. The acrylate group introduced on the surface of the titanium dioxide can improve the adhesive properties with the acrylic resin, thereby improving the durability, water resistance, and abrasion resistance of the composition.

상기 실란 커플링제의 함량은 이산화티탄 100중량부에 대하여 1~10중량부인 것이 바람직하여, 상기 수치범위에서 조성물의 내마모성이 극대화될 수 있다. The content of the silane coupling agent is preferably 1 to 10 parts by weight based on 100 parts by weight of titanium dioxide, so that the abrasion resistance of the composition may be maximized within the numerical range.

상기 탄산칼슘은 도료 조성물의 내마모성 및 내구성을 향상시키기 위하여 사용될 수 있다.The calcium carbonate may be used to improve abrasion resistance and durability of the coating composition.

상기 탄산칼슘의 함량은 아크릴 수지 100중량부에 대하여 50~300중량부인 것이 바람직하며, 함량이 50중량부 미만인 경우 내마모성 및 내구성이 저하되고, 300중량부를 초과하는 경우 가공성 및 내충격성이 저하된다.The content of calcium carbonate is preferably 50 to 300 parts by weight based on 100 parts by weight of the acrylic resin, and when the content is less than 50 parts by weight, abrasion resistance and durability are deteriorated, and when it exceeds 300 parts by weight, processability and impact resistance are deteriorated.

상기 분산제는 조성물의 분산특성을 개선하고 황변도를 저하시키기 위하여 사용되며, 포스폰산계 화합물, 암모니아수 및 물을 반응시켜 제조될 수 있다. The dispersant is used to improve the dispersing properties of the composition and reduce the degree of yellowing, and may be prepared by reacting a phosphonic acid-based compound, aqueous ammonia, and water.

포스폰산계 화합물로는 페닐포스폰산, 이소프로필메틸포스폰산, 2-페닐에틸포스폰산, 아미노메틸포스폰산, 3-아미노프로필포스폰산, 아미노메틸렌 비스포스폰산 등이 사용될 수 있다. As the phosphonic acid-based compound, phenylphosphonic acid, isopropylmethylphosphonic acid, 2-phenylethylphosphonic acid, aminomethylphosphonic acid, 3-aminopropylphosphonic acid, aminomethylene bisphosphonic acid, and the like can be used.

이때 상기 포스폰산계 화합물, 암모니아수 및 물의 중량비는 6:2~8:2~8 인 것이 바람직하다. At this time, the weight ratio of the phosphonic acid-based compound, aqueous ammonia and water is preferably 6:2-8:2-8.

상기 분산제의 함량은 아크릴 수지 100중량부에 대하여 0.1~5중량부인 것이 바람직하며, 함량이 0.1중량부 미만인 경우 황변도가 증가되고, 함량이 5중량부를 초과하면 내구성 및 내마모성이 저하될 수 있다. The content of the dispersant is preferably 0.1 to 5 parts by weight based on 100 parts by weight of the acrylic resin, and if the content is less than 0.1 parts by weight, the degree of yellowing increases, and if the content exceeds 5 parts by weight, durability and abrasion resistance may decrease.

또한 본 발명은 분산제로서 폴리카르복실산 암모늄염을 추가로 사용할 수 있으며, 상기 폴리카르복실산 암모늄염은 폴리카르복실산을 암모니아수와 반응시켜 제조될 수 있다. 이때 폴리카르복실산 암모늄염의 고형분은 20~60중량% 인 것이 바람직하다. In addition, the present invention may further use an ammonium polycarboxylic acid salt as a dispersant, and the ammonium polycarboxylic acid may be prepared by reacting a polycarboxylic acid with aqueous ammonia. At this time, the solid content of the ammonium polycarboxylic acid salt is preferably 20 to 60% by weight.

상기 폴리카르복실산으로는 폴리아크릴산, 폴리메타크릴산, 폴리아크릴산 공중합체, 폴리메타크릴산 공중합체 등이 있다. Examples of the polycarboxylic acid include polyacrylic acid, polymethacrylic acid, polyacrylic acid copolymer, and polymethacrylic acid copolymer.

이때 포스폰산계 화합물 및 폴리카르복실산 암모늄염의 중량비는 60~80:20~40인 것이 바람직하다. 상기 수치범위를 만족하는 경우 조성물의 분산성 및 황변방지특성이 극대화될 수 있다. At this time, the weight ratio of the phosphonic acid-based compound and the polycarboxylic acid ammonium salt is preferably 60 to 80:20 to 40. When the above numerical range is satisfied, the dispersibility and anti-yellowing properties of the composition can be maximized.

상기 폴리스티렌 중공입자는 조성물의 난반사를 유도하고 백색도를 향상시킬 수 있으며, 높은 유리전이온도를 가져 먼지가 달라붙지 않게 하는 효능을 가지고 있다. The hollow polystyrene particles can induce diffuse reflection of the composition and improve whiteness, and have an effect of preventing dust from sticking due to a high glass transition temperature.

상기 폴리스티렌 중공입자의 함량은 아크릴 수지 100중량부에 대하여 0.5~30중량부인 것이 바람직하며, 함량이 0.5중량부 미만인 경우 백색도가 저하되고, 함량이 30중량부를 초과하면 내구성 및 내마모성이 저하될 수 있다. The content of the hollow polystyrene particles is preferably 0.5 to 30 parts by weight based on 100 parts by weight of the acrylic resin, and if the content is less than 0.5 parts by weight, the whiteness decreases, and if the content exceeds 30 parts by weight, durability and abrasion resistance may decrease. .

상기 크랙방지제는 도막의 치밀성, 젖음성 및 부착성을 향상시켜 도막의 크랙 발생을 방지할 수 있으며, 트리프로필렌글리콜 n-부틸에테르, 디프로필렌글리콜 n-부틸에테르 등이 사용될 수 있다. The crack inhibitor may improve the density, wettability and adhesion of the coating film to prevent cracking of the coating film, and tripropylene glycol n-butyl ether, dipropylene glycol n-butyl ether, and the like may be used.

크랙방지제의 함량은 아크릴 수지 100중량부에 대하여 2~20중량부인 것이 바람직하며, 함량이 2중량부 미만인 경우 크랙방지특성이 저하되고, 20중량부를 초과하는 경우 건조속도가 느려진다.The content of the crack inhibitor is preferably 2 to 20 parts by weight based on 100 parts by weight of the acrylic resin, and when the content is less than 2 parts by weight, the crack prevention property is deteriorated, and when it exceeds 20 parts by weight, the drying speed becomes slow.

본 발명은 크랙방지제로서 트리프로필렌글리콜 n-부틸에테르 및 디프로필렌글리콜 n-부틸에테르를 동시에 사용할 수 있으며, 이때 트리프로필렌글리콜 n-부틸에테르 및 디프로필렌글리콜 n-부틸에테르의 중량비는 60~80:20~40인 것이 바람직하다. 상기 수치범위를 만족하는 경우 조성물의 크랙방지특성이 극대화될 수 있다. In the present invention, tripropylene glycol n-butyl ether and dipropylene glycol n-butyl ether may be used simultaneously as a crack inhibitor, wherein the weight ratio of tripropylene glycol n-butyl ether and dipropylene glycol n-butyl ether is 60 to 80: It is preferable that it is 20-40. When the above numerical range is satisfied, the crack prevention property of the composition can be maximized.

또한 본 발명은 크랙방지제로서 폴리카르복실산 2,2,4-트리메틸-1,3-펜탄디올 모노이소부티레이트(텍사놀)를 추가로 사용할 수 있다.In addition, in the present invention, a polycarboxylic acid 2,2,4-trimethyl-1,3-pentanediol monoisobutyrate (texanol) may be further used as a crack inhibitor.

예를 들면, 크랙방지제로서 트리프로필렌글리콜 n-부틸에테르 및 텍사놀을 동시에 사용할 수 있으며, 이때 트리프로필렌글리콜 n-부틸에테르 및 텍사놀의 중량비는 60~80:20~40인 것이 바람직하다. 상기 수치범위를 만족하는 경우 조성물의 크랙방지특성이 극대화될 수 있다. For example, tripropylene glycol n-butyl ether and texanol may be used simultaneously as a crack inhibitor, and the weight ratio of tripropylene glycol n-butyl ether and texanol is preferably 60 to 80:20 to 40. When the above numerical range is satisfied, the crack prevention property of the composition can be maximized.

또한 본 발명은 크랙방지제로서 트리프로필렌글리콜 n-부틸에테르, 디프로필렌글리콜 n-부틸에테르 및 텍사놀을 동시에 사용할 수 있으며, 이때 트리프로필렌글리콜 n-부틸에테르, 디프로필렌글리콜 n-부틸에테르 및 텍사놀의 중량비는 100:40~70:20~50 인 것이 바람직하다. 상기 수치범위를 만족하는 경우 조성물의 크랙방지특성이 극대화될 수 있다. In addition, in the present invention, tripropylene glycol n-butyl ether, dipropylene glycol n-butyl ether, and taxanol may be used simultaneously as a crack inhibitor, and at this time, tripropylene glycol n-butyl ether, dipropylene glycol n-butyl ether and taxanol The weight ratio of is preferably 100:40 ~ 70:20 ~ 50. When the above numerical range is satisfied, the crack prevention property of the composition can be maximized.

또한 상기 조성물은 아크릴레이트기 함유 실란 커플링제 및 아크릴산 모노머의 공중합체를 추가로 포함할 수 있다. In addition, the composition may further include a copolymer of an acrylate group-containing silane coupling agent and an acrylic acid monomer.

상기 공중합체 내에 포함된 다수의 카르복실기는 조성물 내의 성분들의 접착성을 향상시키고, 내마모성, 내열성 및 내수성을 개선할 수 있다. A plurality of carboxyl groups included in the copolymer can improve adhesion of components in the composition, and improve wear resistance, heat resistance, and water resistance.

상기 아크릴레이트기 함유 실란 커플링제로는 3-메타크릴록시프로필메틸디메톡시실란, 3-메타크릴록시프로필트리메톡시실란, 3-메타크릴록시프로필메틸디에톡시실란, 3-메타크릴록시프로필트리에톡시실란, 3-아크릴록시프로필트리메톡시실란, 메타크릴록시메틸트리에톡시실란, 메타크릴록시메틸트리메톡시실란 등이 있다. As the acrylate group-containing silane coupling agent, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, and 3-methacryloxypropyltri Ethoxysilane, 3-acryloxypropyltrimethoxysilane, methacryloxymethyltriethoxysilane, and methacryloxymethyltrimethoxysilane.

상기 아크릴산 모노머는 아크릴산, 메타크릴산, 메틸 아크릴산, 에틸 아크릴산, 부틸 아크릴산, 2-에틸 헥실 아크릴산, 데실아크릴산, 메틸 메타크릴산, 에틸 메타크릴산, 부틸 메타크릴산, 2-에틸 헥실 메타크릴산, 데실메타크릴산 등이 있다. The acrylic acid monomer is acrylic acid, methacrylic acid, methyl acrylic acid, ethyl acrylic acid, butyl acrylic acid, 2-ethyl hexyl acrylic acid, decyl acrylic acid, methyl methacrylic acid, ethyl methacrylic acid, butyl methacrylic acid, 2-ethyl hexyl methacrylic acid , Decyl methacrylic acid, and the like.

상기 아크릴레이트기 함유 실란 커플링제 및 아크릴산 모노머의 중량비는 10~30:70~90인 것이 바람직하며, 상기 수치 범위에서 조성물의 내마모성, 내수성, 내열성 등이 극대화될 수 있다. The weight ratio of the acrylate group-containing silane coupling agent and the acrylic acid monomer is preferably 10 to 30:70 to 90, and abrasion resistance, water resistance, heat resistance, and the like of the composition may be maximized within the above numerical range.

상기 아크릴레이트기 함유 실란 커플링제 및 아크릴산 모노머의 공중합체는 아크릴 수지 100중량부에 대하여 1~10중량부 사용되며, 함량이 1중량부 미만인 경우 첨가의 효과가 미미하고, 10중량부를 초과하는 경우 도막의 건조속도가 저하된다.The copolymer of the acrylate group-containing silane coupling agent and the acrylic acid monomer is used in an amount of 1 to 10 parts by weight based on 100 parts by weight of the acrylic resin. The drying speed of the coating film decreases.

또한 상기 조성물은 아크릴레이트기 함유 실란 커플링제와 포스폰산계 화합물을 반응시켜 제조한 실란 커플링제 올리고머를 추가로 포함할 수 있다. In addition, the composition may further include a silane coupling agent oligomer prepared by reacting an acrylate group-containing silane coupling agent and a phosphonic acid-based compound.

상기 실란 커플링제 올리고머를 사용함으로써 조성물의 접착성 및 황변방지특성을 향상시킬 수 있으며, 도막의 두께를 균일하게 조절할 수 있다.By using the silane coupling agent oligomer, the adhesiveness and anti-yellowing properties of the composition can be improved, and the thickness of the coating film can be uniformly adjusted.

상기 아크릴레이트기 함유 실란 커플링제로는 3-메타크릴록시프로필메틸디메톡시실란, 3-메타크릴록시프로필트리메톡시실란, 3-메타크릴록시프로필메틸디에톡시실란, 3-메타크릴록시프로필트리에톡시실란, 3-아크릴록시프로필트리메톡시실란, 메타크릴록시메틸트리에톡시실란, 메타크릴록시메틸트리메톡시실란 등이 있다. As the acrylate group-containing silane coupling agent, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, and 3-methacryloxypropyltri Ethoxysilane, 3-acryloxypropyltrimethoxysilane, methacryloxymethyltriethoxysilane, and methacryloxymethyltrimethoxysilane.

상기 포스폰산계 화합물로는 페닐포스폰산, 이소프로필메틸포스폰산, 2-페닐에틸포스폰산, 아미노메틸포스폰산, 3-아미노프로필포스폰산, 아미노메틸렌 비스포스폰산 등이 사용될 수 있다.As the phosphonic acid-based compound, phenylphosphonic acid, isopropylmethylphosphonic acid, 2-phenylethylphosphonic acid, aminomethylphosphonic acid, 3-aminopropylphosphonic acid, aminomethylene bisphosphonic acid, and the like may be used.

아크릴레이트기 함유 실란 커플링제와 포스폰산계 화합물의 중량비는 60~80:20~40인 것이 바람직하며, 상기 범위를 만족하는 경우 조성물의 접착성 및 황변방지특성이 극대화될 수 있다. The weight ratio of the acrylate group-containing silane coupling agent and the phosphonic acid-based compound is preferably 60 to 80:20 to 40, and when the above range is satisfied, the adhesiveness and anti-yellowing properties of the composition can be maximized.

실란 커플링제 올리고머의 중량평균분자량은 1,000~10,000g/mol이 바람직하며, 실란 커플링제 올리고머는 아크릴 수지 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하다. 함량이 1중량부 미만인 경우 첨가의 효과가 미미하고, 함량이 10중량부를 초과하는 경우 작업성이 저하되고 도막의 두께가 불균일하게 된다. The weight average molecular weight of the silane coupling agent oligomer is preferably 1,000 to 10,000 g/mol, and the silane coupling agent oligomer is preferably used in an amount of 1 to 10 parts by weight based on 100 parts by weight of the acrylic resin. When the content is less than 1 part by weight, the effect of the addition is insignificant, and when the content is more than 10 parts by weight, workability decreases and the thickness of the coating film becomes non-uniform.

또한 상기 조성물은 에폭시기 함유 실란 커플링제와 트리프로필렌글리콜 n-부틸에테르 또는 디프로필렌글리콜 n-부틸에테르를 반응시켜 제조한 실란 커플링제 올리고머를 추가로 포함할 수 있다. In addition, the composition may further include a silane coupling agent oligomer prepared by reacting an epoxy group-containing silane coupling agent with tripropylene glycol n-butyl ether or dipropylene glycol n-butyl ether.

상기 실란 커플링제 올리고머를 사용함으로써 조성물의 접착성 및 크랙방지특성을 향상시킬 수 있으며, 도막의 두께를 균일하게 조절할 수 있다.By using the silane coupling agent oligomer, it is possible to improve adhesion and crack prevention properties of the composition, and to uniformly control the thickness of the coating film.

에폭시기 함유 실란 커플링제로는 2-글리시독시에틸메틸디메톡시실란, 2-글리시독시에틸메틸디에톡시실란, 3-글리시독시프로필메틸디메톡시실란, 3-글리시독시프로필메틸디에톡시실란 등의 글리시독시 C1-4 알킬 C1-4 알킬 C1-4 알콕시실란; 2-글리시독시에틸트리메톡시실란, 2-글리시독시에틸트리에톡시실란, 3-글리시독시프로필트리메톡시실란, 3-글리시독시프로필트리에톡시실란 등의 글리시독시 C1-4 알킬 C1-4 알콕시실란; 2-(3,4-에폭시시클로헥실)에틸메틸디메톡시실란, 2-(3,4-에폭시시클로헥실)에틸메틸디에톡시실란, 3-(3,4-에폭시시클로헥실)프로필메틸디메톡시실란, 3-(3,4-에폭시시클로헥실)프로필메틸디에톡시실란 등의 에폭시 C3-10 시클로알킬 C1-4 알킬 C1-4 알킬 C1-4 알콕시실란; 2-(3,4-에폭시시클로헥실)에틸트리메톡시실란, 2-(3,4-에폭시시클로헥실)에틸트리에톡시실란, 3-(3,4-에폭시시클로헥실)프로필트리메톡시실란, 3-(3,4-에폭시시클로헥실)프로필트리에톡시실란 등의 에폭시 C3-10 시클로알킬 C1-4 알킬 C1-4 알콕시실란 등이 있다. The epoxy group-containing silane coupling agent is 2-glycidoxyethylmethyldimethoxysilane, 2-glycidoxyethylmethyldiethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, and 3-glycidoxypropylmethyldiethoxysilane. Glycidoxy C 1-4 alkyl C 1-4 alkyl C 1-4 alkoxysilane such as; Glycidoxy C 1 such as 2-glycidoxyethyltrimethoxysilane, 2-glycidoxyethyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, and 3-glycidoxypropyltriethoxysilane -4 alkyl C 1-4 alkoxysilane; 2-(3,4-epoxycyclohexyl)ethylmethyldimethoxysilane, 2-(3,4-epoxycyclohexyl)ethylmethyldiethoxysilane, 3-(3,4-epoxycyclohexyl)propylmethyldimethoxysilane Epoxy C 3-10 cycloalkyl C 1-4 alkyl C 1-4 alkyl C 1-4 alkoxysilane such as 3-(3,4-epoxycyclohexyl)propylmethyldiethoxysilane; 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 3-(3,4-epoxycyclohexyl)propyltrimethoxysilane And epoxy C 3-10 cycloalkyl C 1-4 alkyl C 1-4 alkoxysilanes such as 3-(3,4-epoxycyclohexyl)propyltriethoxysilane.

에폭시기 함유 실란 커플링제와 트리프로필렌글리콜 n-부틸에테르 또는 디프로필렌글리콜 n-부틸에테르의 중량비는 60~80:20~40인 것이 바람직하며, 상기 범위를 만족하는 경우 조성물의 접착성 및 크랙방지특성이 극대화될 수 있다. The weight ratio of the epoxy group-containing silane coupling agent and tripropylene glycol n-butyl ether or dipropylene glycol n-butyl ether is preferably 60 to 80:20 to 40, and when the above range is satisfied, the adhesiveness and crack prevention properties of the composition Can be maximized.

실란 커플링제 올리고머의 중량평균분자량은 1,000~10,000g/mol이 바람직하며, 실란 커플링제 올리고머는 아크릴 수지 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하다. 함량이 1중량부 미만인 경우 첨가의 효과가 미미하고, 함량이 10중량부를 초과하는 경우 작업성이 저하되고 도막의 두께가 불균일하게 된다. The weight average molecular weight of the silane coupling agent oligomer is preferably 1,000 to 10,000 g/mol, and the silane coupling agent oligomer is preferably used in an amount of 1 to 10 parts by weight based on 100 parts by weight of the acrylic resin. When the content is less than 1 part by weight, the effect of the addition is insignificant, and when the content is more than 10 parts by weight, workability decreases and the thickness of the coating film becomes non-uniform.

또한 상기 도료 조성물을 포함하는 제품에 있어서, 상기 제품은 도료, 코팅제 또는 접착제인 것을 특징으로 한다. In addition, in the product comprising the coating composition, the product is characterized in that the coating material, coating agent or adhesive.

본 발명의 도료 조성물은 공지의 방법, 예를 들면 솔, 롤 코팅, 스프레이 코팅, 함침 등의 방법으로 기재 또는 노면 상에 도포되거나 코팅될 수 있다. The coating composition of the present invention may be applied or coated on a substrate or road surface by a known method, for example, brush, roll coating, spray coating, or impregnation.

도막의 두께는 특별히 한정되지 않으며, 용도에 따라 0.1㎛~20mm 두께로 조절될 수 있다. The thickness of the coating film is not particularly limited, and may be adjusted to a thickness of 0.1 μm to 20 mm depending on the application.

본 발명의 도료 조성물로부터 제조된 도막은 건조속도가 빠르고, 황변도가 낮으며, 친환경적이고, 경도, 접착성, 내마모성, 내후성, 내수성, 내열성, 내충격성 등이 우수하다. The coating film prepared from the coating composition of the present invention has a fast drying speed, low yellowing degree, is eco-friendly, and has excellent hardness, adhesion, abrasion resistance, weather resistance, water resistance, heat resistance, and impact resistance.

이하 실시예 및 비교예를 통해 본 발명을 상세히 설명한다. 하기 실시예는 본 발명의 실시를 위하여 예시된 것일 뿐, 본 발명의 내용이 하기 실시예에 의하여 한정되는 것은 아니다.The present invention will be described in detail through examples and comparative examples below. The following examples are only illustrated for the practice of the present invention, and the contents of the present invention are not limited by the following examples.

(실시예 1)(Example 1)

페닐포스폰산, 28% 암모니아수 및 물을 6:6:6 의 중량비로 반응시켜 분산제를 제조하였다. Phenylphosphonic acid, 28% aqueous ammonia, and water were reacted in a weight ratio of 6:6:6 to prepare a dispersant.

폴리메틸메타크릴레이트 에멀젼 수지(고형분 48중량%) 100중량부, 이산화티탄 20중량부, 탄산칼슘 150중량부, 분산제 1중량부, 폴리스티렌 중공입자 10중량부 및 트리프로필렌글리콜 n-부틸에테르 10중량부를 혼합하여 도료 조성물을 제조하였다. Polymethylmethacrylate emulsion resin (solid content 48% by weight) 100 parts by weight, titanium dioxide 20 parts by weight, calcium carbonate 150 parts by weight, dispersant 1 part by weight, polystyrene hollow particles 10 parts by weight, and tripropylene glycol n-butyl ether 10 parts by weight The parts were mixed to prepare a coating composition.

(실시예 2)(Example 2)

트리프로필렌글리콜 n-부틸에테르 1중량부를 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 도료 조성물을 제조하였다. A coating composition was prepared in the same manner as in Example 1, except that 1 part by weight of tripropylene glycol n-butyl ether was used.

(실시예 3)(Example 3)

트리프로필렌글리콜 n-부틸에테르 25중량부를 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 도료 조성물을 제조하였다. A coating composition was prepared in the same manner as in Example 1, except that 25 parts by weight of tripropylene glycol n-butyl ether was used.

(실시예 4)(Example 4)

디프로필렌글리콜 n-부틸에테르 5중량부를 추가로 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 도료 조성물을 제조하였다. A coating composition was prepared in the same manner as in Example 1, except that 5 parts by weight of dipropylene glycol n-butyl ether was additionally used.

(실시예 5)(Example 5)

디프로필렌글리콜 n-부틸에테르 5중량부 및 텍사놀 3중량부를 추가로 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 도료 조성물을 제조하였다. A coating composition was prepared in the same manner as in Example 1, except that 5 parts by weight of dipropylene glycol n-butyl ether and 3 parts by weight of taxanol were additionally used.

(실시예 6)(Example 6)

3-메타크릴록시프로필트리메톡시실란 70중량부와 페닐포스폰산 30중량부를 60℃에서 24시간 반응시켜 중량평균분자량이 5,000g/mol인 실란 커플링제 올리고머를 제조하였다. 70 parts by weight of 3-methacryloxypropyltrimethoxysilane and 30 parts by weight of phenylphosphonic acid were reacted at 60° C. for 24 hours to prepare a silane coupling agent oligomer having a weight average molecular weight of 5,000 g/mol.

상기 실란 커플링제 올리고머 3중량부를 추가로 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 도료 조성물을 제조하였다. A coating composition was prepared in the same manner as in Example 1, except that 3 parts by weight of the silane coupling agent oligomer was additionally used.

(비교예 1)(Comparative Example 1)

트리프로필렌글리콜 n-부틸에테르 10중량부 대신에, 텍사놀 10중량부를 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 도료 조성물을 제조하였다.A coating composition was prepared in the same manner as in Example 1, except that 10 parts by weight of taxanol was used instead of 10 parts by weight of tripropylene glycol n-butyl ether.

상기 실시예 및 비교예로부터 제조된 도료 조성물로부터 도막을 형성한 후, 불점착 건조성, 내수성, 내마모성, 휘도율 및 황변도를 측정하여 그 결과를 아래의 표 1에 나타내었다. After forming a coating film from the coating composition prepared from the above Examples and Comparative Examples, non-adhesive dryness, water resistance, abrasion resistance, luminance rate, and yellowness were measured, and the results are shown in Table 1 below.

불점착 건조성은 KS M 6080에 의거하여 측정하였으며, 도료가 불점착 시험기의 타이어에 붙지 않는 시간을 측정하였다.Non-adhesive dryness was measured according to KS M 6080, and the time at which the paint did not stick to the tire of the non-adhesive tester was measured.

내수성은 KS M ISO 1514에 의거하여 측정하였으며, 72시간 건조 후 물에 침지시켜 24시간 동안 방치한 후 꺼내어 상온에서 2시간 건조시켜 도막의 상태를 관찰하였다. 이때 도막의 상태를 탁월, 우수, 보통, 불량으로 표기하였다. Water resistance was measured according to KS M ISO 1514, and after drying for 72 hours, immersed in water, left for 24 hours, taken out, and dried at room temperature for 2 hours to observe the state of the coating film. At this time, the state of the coating film was marked as excellent, excellent, moderate, and poor.

내마모도는 KS M 6080에 의거하여 측정하였으며 교통량 등급 P7(400만 바퀴 통과) 후 재귀반사도를 측정하였다. 내마모도는 흰색의 경우 100만 바퀴가 통과한 후 건조한 상태에서 재귀반사도 성능 (RL)에 따라 R3≥150, R4≥200, R5≥300으로 표시한다.Wear resistance was measured according to KS M 6080, and retroreflectivity was measured after traffic level P7 (passing 4 million laps). Wear resistance is expressed as R3≥150, R4≥200, and R5≥300 according to the retroreflectivity performance (RL) in a dry state after passing 1 million wheels in white.

휘도율은 KS M 6080에 의거하여 측정하였다. The luminance rate was measured according to KS M 6080.

황변도는 도막을 100℃ 오븐에서 24시간 동안 방치한 후 꺼내어 변색 정도를 관찰하여 탁월, 우수, 보통, 불량으로 표기하였다. As for the degree of yellowness, the coating film was left in an oven at 100° C. for 24 hours, taken out, and the degree of discoloration was observed, and marked as excellent, excellent, moderate, and poor.

구분division 실시예Example 비교예Comparative example 1One 22 33 44 55 66 1One 불점착 건조성
(분)
Non-stick dryness
(minute)
55 1010 1010 55 55 55 2020
내수성Water resistance 우수Great 보통usually 보통usually 탁월eminence 탁월eminence 탁월eminence 불량Bad 내마모도
(마른상태) P7 (400만회)
Wear resistance
(Dry state) P7 (4 million times)
R5R5 R4R4 R4R4 R5R5 R5R5 R5R5 R4R4
휘도율Luminance factor 9090 8787 8686 9090 9090 9090 8282 황변도Yellowness 우수Great 보통usually 보통usually 탁월eminence 탁월eminence 탁월eminence 불량Bad

상기 표 1의 결과로부터, 실시예 1 내지 6은 불점착 건조성, 내수성, 내마모성 및 황변도가 우수하며, 특히 실시예 4 내지 6은 상기 특성이 가장 우수하다. From the results of Table 1, Examples 1 to 6 are excellent in non-adhesive dryness, water resistance, abrasion resistance, and yellowing, and in particular, Examples 4 to 6 have the most excellent properties.

반면 비교예 1은 상기 특성이 실시예에 비하여 불량함을 알 수 있다. On the other hand, it can be seen that the characteristics of Comparative Example 1 are poorer than that of the Example.

Claims (5)

아크릴 수지; 이산화티탄; 탄산칼슘; 분산제; 폴리스티렌 중공입자; 및 크랙방지제를 포함하는 도료 조성물에 있어서,
상기 아크릴 수지 100중량부에 대하여 이산화티탄 3~100중량부, 탄산칼슘 50~300중량부, 분산제 0.1~5중량부, 폴리스티렌 중공입자 0.5~30중량부 및 크랙방지제 2~20중량부를 포함하고,
상기 크랙방지제는 트리프로필렌글리콜 n-부틸에테르 또는 디프로필렌글리콜 n-부틸에테르인 것을 특징으로 하는 도료 조성물.
Acrylic resin; Titanium dioxide; Calcium carbonate; Dispersant; Hollow polystyrene particles; And in the coating composition comprising a crack inhibitor,
Including 3 to 100 parts by weight of titanium dioxide, 50 to 300 parts by weight of calcium carbonate, 0.1 to 5 parts by weight of dispersant, 0.5 to 30 parts by weight of polystyrene hollow particles and 2 to 20 parts by weight of crack inhibitor, based on 100 parts by weight of the acrylic resin,
The crack inhibitor is a coating composition, characterized in that tripropylene glycol n-butyl ether or dipropylene glycol n-butyl ether.
삭제delete 제1항에 있어서,
상기 아크릴 수지 100중량부에 대하여 아크릴레이트기 함유 실란 커플링제 및 아크릴산 모노머의 공중합체 1~10중량부를 추가로 포함하는 것을 특징으로 하는 도료 조성물.
The method of claim 1,
A coating composition, characterized in that it further comprises 1 to 10 parts by weight of a copolymer of an acrylate group-containing silane coupling agent and an acrylic acid monomer based on 100 parts by weight of the acrylic resin.
삭제delete 제1항의 도료 조성물을 포함하는 제품에 있어서, 상기 제품은 도료, 코팅제 또는 접착제인 것을 특징으로 하는 제품.

A product comprising the coating composition of claim 1, wherein the product is a paint, coating or adhesive.

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100888704B1 (en) * 2008-06-19 2009-03-16 대동안전주식회사 Adhesive paint composition for road marker
KR101558876B1 (en) 2015-04-02 2015-10-15 주식회사 정석케미칼 Water soluble paint composition for a road marking with improved wear resistance
KR101901915B1 (en) * 2018-03-14 2018-09-27 (주)삼지테크인 A water soluble paint composition for road marking
KR102112309B1 (en) * 2019-12-17 2020-06-03 삼지산물(주) A room temperature curing paint composition with fast drying rate

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100888704B1 (en) * 2008-06-19 2009-03-16 대동안전주식회사 Adhesive paint composition for road marker
KR101558876B1 (en) 2015-04-02 2015-10-15 주식회사 정석케미칼 Water soluble paint composition for a road marking with improved wear resistance
KR101901915B1 (en) * 2018-03-14 2018-09-27 (주)삼지테크인 A water soluble paint composition for road marking
KR102112309B1 (en) * 2019-12-17 2020-06-03 삼지산물(주) A room temperature curing paint composition with fast drying rate

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