KR20120097817A - Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same - Google Patents

Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same Download PDF

Info

Publication number
KR20120097817A
KR20120097817A KR1020110017277A KR20110017277A KR20120097817A KR 20120097817 A KR20120097817 A KR 20120097817A KR 1020110017277 A KR1020110017277 A KR 1020110017277A KR 20110017277 A KR20110017277 A KR 20110017277A KR 20120097817 A KR20120097817 A KR 20120097817A
Authority
KR
South Korea
Prior art keywords
coating composition
curable coating
aliphatic urethane
molded article
urethane acrylate
Prior art date
Application number
KR1020110017277A
Other languages
Korean (ko)
Other versions
KR101210905B1 (en
Inventor
김강수
김장욱
박규엽
Original Assignee
주식회사 케이씨씨
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 주식회사 케이씨씨 filed Critical 주식회사 케이씨씨
Priority to KR1020110017277A priority Critical patent/KR101210905B1/en
Publication of KR20120097817A publication Critical patent/KR20120097817A/en
Application granted granted Critical
Publication of KR101210905B1 publication Critical patent/KR101210905B1/en

Links

Classifications

    • 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
    • C09D4/00Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60QARRANGEMENT OF SIGNALLING OR LIGHTING DEVICES, THE MOUNTING OR SUPPORTING THEREOF OR CIRCUITS THEREFOR, FOR VEHICLES IN GENERAL
    • B60Q1/00Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor
    • B60Q1/02Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor the devices being primarily intended to illuminate the way ahead or to illuminate other areas of way or environments
    • B60Q1/04Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor the devices being primarily intended to illuminate the way ahead or to illuminate other areas of way or environments the devices being headlights
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • 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
    • C08K5/10Esters; Ether-esters
    • C08K5/11Esters; Ether-esters of acyclic polycarboxylic acids
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/29Compounds containing one or more carbon-to-nitrogen double bonds
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3472Five-membered rings
    • C08K5/3475Five-membered rings condensed with carbocyclic rings
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • C08L75/14Polyurethanes having carbon-to-carbon unsaturated bonds
    • 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/14Polyurethanes having carbon-to-carbon unsaturated bonds
    • 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
    • C09D7/48Stabilisers against degradation by oxygen, light or heat
    • 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
    • C09D7/63Additives non-macromolecular organic
    • 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
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2369/00Characterised by the use of polycarbonates; Derivatives of polycarbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2475/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2475/04Polyurethanes
    • C08J2475/14Polyurethanes having carbon-to-carbon unsaturated bonds

Landscapes

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

Abstract

PURPOSE: A UV-curable paint composition is provided to have excellent adhesion to polycarbonate material, heat resistance, abrasion resistance, hardness, chipping resistance, and weatherability. CONSTITUTION: A UV-curable paint composition comprises polyfunctional aliphatic urethane acrylate oligomer having six or more polymerizable functional groups, a Benzotriazole-modified aliphatic urethane acrylate oligomer, a polyfunctional acrylate monomer, a photopolymerization initiator, a UV-absorbing agent, and a photostabilizer. The polyfunctional aliphatic urethane acrylate oligomer is a reaction product of a bifunctional isocyanate compound, hydroxy acrylate monomer containing three or more polymerizable unsaturated groups per a molecule.

Description

플라스틱 기재의 표면코팅용으로서 유용한 자외선 경화형 도료 조성물 및 그로부터 형성된 경화코팅층을 포함하는 성형품{UV-CURABLE COATING COMPOSITION USEFUL AS TOP SURFACE COATING FOR PLASTIC SUBSTRATE AND MOLDED ARTICLE COMPRISNG A CURED COATING LAYER FORMED FROM THE SAME}UV-CURABLE COATING COMPOSITION USEFUL AS TOP SURFACE COATING FOR PLASTIC SUBSTRATE AND MOLDED ARTICLE COMPRISNG A CURED COATING LAYER FORMED FROM THE SAME}

본 발명은 플라스틱 기재의 표면피복용으로서 유용한 자외선 경화형 도료 조성물 및 그로부터 형성된 경화코팅층을 포함하는 성형품에 관한 것으로서, 보다 상세하게는, 6관능기 이상의 다관능성 지방족 우레탄 아크릴레이트 올리고머, 벤조트리아졸 변성 지방족 우레탄 아크릴레이트 올리고머, 다관능성 아크릴레이트 모노머, 광중합 개시제, 자외선 흡수제 및 광안정제를 포함하며, 플라스틱 소재, 특히 폴리카보네이트(PC) 소재에 대한 부착성 및 내열성이 우수하고 내마모성, 고경도, 내chipping성 및 내후성이 뛰어나 플라스틱 기재, 특히 자동차 헤드램프(Head Lamp)의 PC 렌즈와 같은 유리대체품용 플라스틱 소재의 표면피복용으로서 유용한 자외선 경화형 도료 조성물 및 그로부터 형성된 경화코팅층을 포함하는 성형품에 관한 것이다.The present invention relates to a molded article comprising an ultraviolet curable coating composition useful for surface coating of a plastic substrate and a cured coating layer formed therefrom, and more particularly, a multifunctional aliphatic urethane acrylate oligomer or a benzotriazole modified aliphatic urethane. It includes acrylate oligomers, polyfunctional acrylate monomers, photopolymerization initiators, ultraviolet absorbers and light stabilizers, and has excellent adhesion and heat resistance to plastic materials, in particular polycarbonate (PC) materials, and abrasion resistance, high hardness, chipping resistance and The present invention relates to a molded article comprising an ultraviolet curable coating composition having excellent weather resistance and useful for surface coating of a plastic material for glass replacement products, such as a PC lens of an automobile head lamp, in particular, a cured coating layer formed therefrom.

종래의 자동차 헤드램프 시장은 헤드램프 커버(cover)로 유리를 사용하였다. 그러나 자동차의 연비 개선을 위한 소재의 경량화와 생산 비용 절감을 위한 원가 개선을 위해서 현재 생산 되는 모든 헤드램프 커버에는 투명성과 성형성이 뛰어난 플라스틱, 특히 폴리카보네이트 소재를 사용하고 있다. The conventional automotive headlamp market has used glass as the headlamp cover. However, in order to reduce the weight of the material for improving fuel efficiency of the automobile and to reduce the cost for reducing the production cost, all headlamp covers that are produced are made of plastic, especially polycarbonate, which has excellent transparency and formability.

그러나, 일반적으로 자동차 헤드램프 렌즈에 적용되는 폴리카보네이트 소재의 경우 투명성 및 내충격성이 우수하나, 내스크래치성, 내후성 그리고 내화학성이 열악하다. 이에 폴리카보네이트 소재의 취약점인 내스크래치성 및 내후성을 보완하기 위해 내후성 및 내스크래치성이 우수한 도료 조성물로 도장하는 하드코팅 도장 공정이 필요하다. However, polycarbonate materials generally applied to automotive headlamp lenses have excellent transparency and impact resistance, but are poor in scratch resistance, weather resistance and chemical resistance. In order to compensate for the scratch resistance and weather resistance, which are weak points of the polycarbonate material, a hard coat coating process for coating with a coating composition having excellent weather resistance and scratch resistance is required.

내스크래치성 향상을 위해 다관능 우레탄 아크릴레이트 올리고머를 사용하는 예가 한국특허공보 제10-0199908호에 개시되어 있다. 그러나 이 조성물의 경우, 도막내 분자간의 수축응력으로 경우 장기간 옥외 환경에 폭로, 방치할 경우 도막의 크랙 및 황변이 심하게 발생하여 도막의 외관 손상 및 부착성 저하, 변색 등을 야기하는 문제가 있다. An example of using a polyfunctional urethane acrylate oligomer for improving scratch resistance is disclosed in Korean Patent Publication No. 10-0199908. However, in the case of this composition, the shrinkage stress between molecules in the coating film causes exposure to the outdoor environment for a long time, and if left unchecked, cracks and yellowing of the coating film occur severely, resulting in damage to the appearance of the coating film, deterioration in adhesion, and discoloration.

한국공개특허공보 제10-1999-0073009호에는 우레탄 아크릴레이트 올리고머 또는 미반응성 열가소성 아크릴 수지를 사용하는 도료 조성물이 개시되어 있으나, 이 조성물의 경우 내스크래치성 및 내열성의 저하로 도막의 본래 목적을 달성하지 못하는 문제가 있다. Korean Laid-Open Patent Publication No. 10-1999-0073009 discloses a coating composition using a urethane acrylate oligomer or an unreactive thermoplastic acrylic resin. However, in the case of this composition, the original purpose of the coating film is achieved due to a decrease in scratch resistance and heat resistance. There is a problem that can not.

요컨대, 종래의 자외선 경화형 도료 조성물들은 가혹한 옥외 환경조건하에서 자외선, 열 및 스크래치 유발물질에 장기간 노출되는 플라스틱 성형품, 특히 자동차 헤드램프 렌즈의 표면피복 용도로는 적합하지 않다.In short, conventional UV curable coating compositions are not suitable for surface coating applications of plastic molded articles, especially automotive headlamp lenses, which are subject to prolonged exposure to UV, heat and scratch causing materials under harsh outdoor environmental conditions.

본 발명은 상기한 종래 기술의 문제점들을 해결하고자 한 것으로서, 성형품표면에 피복되어 장기간 옥외 환경에서의 사용시에도 성형품 자체의 열화를 충분히 방지할 수 있음과 동시에 내스크래치성, 고경도, 도막의 밀착성, 내크랙성이 뛰어나며 특히 Chipping성 등이 뛰어나 투명 플라스틱 렌즈 등의 투명성 소재, 특히 자동차 헤드램프 렌즈의 표면 코팅용으로 특히 효과적인 자외선 경화형 도료 조성물 및 그로부터 형성된 경화코팅층을 포함하는 성형품(예컨대, 자동차 헤드램프용 PC 렌즈)을 제공하는 것을 그 기술적 과제로 한다.The present invention has been made to solve the above problems of the prior art, it is coated on the surface of the molded article can prevent the deterioration of the molded article itself even when used in outdoor environment for a long time and at the same time scratch resistance, high hardness, adhesion of the coating film, Molded article (e.g. automobile headlamps) comprising a UV-curable coating composition and a cured coating layer formed thereon, which are particularly effective for the surface coating of a transparent material such as a transparent plastic lens, particularly an automotive headlamp lens due to excellent crack resistance and excellent chipping resistance. It is a technical subject to provide the PC lens for a camera.

상기한 기술적 과제를 해결하고자 본 발명은, (A) 6개 이상의 중합성 관능기를 갖는 다관능성 지방족 우레탄 아크릴레이트 올리고머, (B) 벤조트리아졸 변성 지방족 우레탄 아크릴레이트 올리고머, (C) 다관능성 아크릴레이트 모노머, (D) 광중합 개시제, (E) 자외선 흡수제 및 (F) 광안정제를 포함하는 자외선 경화형 도료 조성물을 제공한다.The present invention to solve the above technical problem, (A) a polyfunctional aliphatic urethane acrylate oligomer having six or more polymerizable functional groups, (B) benzotriazole modified aliphatic urethane acrylate oligomer, (C) polyfunctional acrylate Provided are an ultraviolet curable coating composition comprising a monomer, (D) a photopolymerization initiator, (E) an ultraviolet absorber, and (F) an optical stabilizer.

본 발명의 다른 측면에 따르면, 상기한 본 발명의 자외선 경화형 도료 조성물로부터 형성된 경화코팅층을 포함하는 성형품이 제공된다.According to another aspect of the present invention, there is provided a molded article comprising a cured coating layer formed from the above-described ultraviolet curable coating composition of the present invention.

본 발명에 따른 자외선 경화형 도료 조성물은 플라스틱 소재, 특히 폴리카보네이트(PC) 소재에 대한 부착성 및 내열성이 우수하고 내마모성, 고경도, 내chipping성 및 내후성이 뛰어나 가혹한 옥외 장기사용의 조건에서도 도막의 내구성을 유지할 수 있어 투명 플라스틱 렌즈, 특히 자동차 헤드램프의 PC 렌즈와 같은 등의 투명성 소재의 표면 코팅용으로 매우 유용하다.The UV curable coating composition according to the present invention has excellent adhesion and heat resistance to plastic materials, especially polycarbonate (PC) materials, and has excellent abrasion resistance, high hardness, chipping resistance and weather resistance, and the durability of the coating film even under severe outdoor long-term use conditions. It is very useful for surface coating of transparent plastic lens, especially transparent material such as PC lens of automobile headlamp.

이하에서 본 발명을 구체적으로 설명한다.Hereinafter, the present invention will be described in detail.

(A) (A) 다관능성Multifunctional 지방족 우레탄  Aliphatic Urethane 아크릴레이트Acrylate 올리고머Oligomer

본 발명의 자외선 경화형 도료 조성물에 포함되는 다관능성 지방족 우레탄 아크릴레이트 올리고머는 중합이 가능한 불포화 그룹인 중합성 관능기를 6개 이상(예컨대 6 내지 15개) 가지며, 도막의 내스크래치성 및 경도를 위해 사용되는 성분이다. 올리고머 (A) 한 분자 내의 중합성 관능기 수가 6미만이면 도막의 경도가 약해져 연필 경도가 2H 이상의 도막을 얻기 힘들고 스틸울 내스크래치성 시험을 통과 할 수 없으며, 내 chipping성 물성 시험 후 도막의 깨짐이 발생할 수 있는 문제점이 있다.The polyfunctional aliphatic urethane acrylate oligomer included in the ultraviolet curable coating composition of the present invention has 6 or more (eg 6 to 15) polymerizable functional groups which are unsaturated groups capable of polymerization, and is used for scratch resistance and hardness of the coating film. It is an ingredient. Oligomer (A) When the number of polymerizable functional groups in one molecule is less than 6, the hardness of the coating film becomes weak and it is difficult to obtain a coating film with pencil hardness of 2H or more, and it cannot pass the steel wool scratch resistance test, and the crack of the coating film after the chipping resistance test There is a problem that can occur.

상기 다관능성 지방족 우레탄 아크릴레이트 올리고머(A)로는, 예컨대, 2관능의 지방족 이소시아네이트의 화합물(예를 들면, 헥사메틸렌 디이소시아네이트, 디사이클로헥실메탄 디이소시아네이트, 이소포론 디이소시아네이트 등)과 중합이 가능한 불포화 그룹을 분자당 3개 이상 함유하는 하이드록시 아크릴레이트 모노머(예를 들어, 펜타에리스리톨 트리아크릴레이트, 디펜타에리스리톨 트리아크릴레이트 등)와의 반응생성물을 사용할 수 있다. 성분(A)의 중량평균분자량으로는 1000~2000 이 바람직하다. 성분(A)의 구체적인 예로는 미원상사㈜의 PU610, SK-Cytec 社의 Ebecryl 1290, Bayer 社의 U400, Double Bond Chemical 社의 DM 87A 등을 들 수 있다.As said polyfunctional aliphatic urethane acrylate oligomer (A), Unsaturation which can superpose | polymerize with the compound of bifunctional aliphatic isocyanate (for example, hexamethylene diisocyanate, dicyclohexyl methane diisocyanate, isophorone diisocyanate etc.) is possible, for example. Reaction products with hydroxy acrylate monomers (eg, pentaerythritol triacrylate, dipentaerythritol triacrylate, etc.) containing three or more groups per molecule can be used. As a weight average molecular weight of component (A), 1000-2000 are preferable. Specific examples of component (A) include PU610 of Miwon Corp., Ebecryl 1290 of SK-Cytec, U400 of Bayer, DM 87A of Double Bond Chemical, and the like.

본 발명의 자외선 경화형 도료 조성물에는 상기 성분(A)가, 유기용매를 제외한 조성물 성분 총합을 기준으로, 바람직하게는 30~60 중량%가, 보다 바람직하게는 45~55 중량%가 포함된다. 조성물 내 성분(A)의 함량이, 유기용매를 제외한 조성물 성분 총합을 기준으로 30 중량% 미만이면 경화도막의 형성이 어렵고, 경화성 및 내스크래치성이 떨어지며, 반대로 60 중량%를 초과하면 과도한 경화밀도에 의해 도막에 크랙이 유발될 수 있다. In the ultraviolet curable coating composition of the present invention, the component (A) is preferably 30 to 60% by weight, more preferably 45 to 55% by weight based on the total composition of the composition excluding the organic solvent. When the content of component (A) in the composition is less than 30% by weight based on the total composition of the composition excluding the organic solvent, it is difficult to form a cured coating film, and the curability and scratch resistance are poor. This may cause cracks in the coating film.

(B) (B) 벤조트리아졸Benzotriazole 변성 지방족 우레탄  Modified aliphatic urethane 아크릴레이트Acrylate 올리고머Oligomer

본 발명의 자외선 경화형 도료 조성물에 포함되는 벤조트리아졸 변성 지방족 우레탄 아크릴레이트 올리고머는 하이드록시기를 가지는 벤조트리아졸과 이소시아네이트, 그리고 아크릴레이트 화합물과의 반응에 의해 생성된 것으로서, 도막의 내후성, 내산화성을 위해 사용되는 성분이다. 도막의 내후성 및 내산화성을 고려하였을 때, 성분(B)의 중량평균분자량은 800~1500 인 것이 바람직하다.The benzotriazole-modified aliphatic urethane acrylate oligomer included in the ultraviolet curable coating composition of the present invention is produced by the reaction between a benzotriazole having a hydroxy group, an isocyanate and an acrylate compound, and the weather resistance and oxidation resistance of the coating film. It is an ingredient used for. In consideration of the weather resistance and oxidation resistance of the coating film, the weight average molecular weight of the component (B) is preferably 800 to 1500.

상기 벤조트리아졸 변성 지방족 우레탄 아크릴레이트 올리고머(B)로는, 예컨대, 2관능의 지방족 이소시아네이트의 화합물(예를 들면, 헥사메틸렌 디이소시아네이트, 디사이클로헥실메탄 디이소시아네이트, 이소포론 디이소시아네이트 등)과 중합이 가능한 불포화 그룹을 분자당 2개 이하로 함유하는 하이드록시 아크릴레이트 모노머(예를 들어, 하이드록시에틸 아크릴레이트, 하이드록시프로필 아크릴레이트, 하이드록시에틸 메타크릴레이트, 하이드록시부틸 아크릴레이트, 하이드록시펜틸 아크릴레이트, 하이드록시부틸 메타크릴레이트 등)와의 반응생성물인 지방족 우레탄 아크릴레이트 올리고머를, 하이드록시기를 가지는 벤조트리아졸 변성 아크릴레이트와 반응시켜 얻어진 것을 사용할 수 있다. 본 발명에서 사용가능한 벤조트리아졸 변성 아크릴레이트의 구체예로는 Otsuka 社의 RUVA-93을 들 수 있다.Examples of the benzotriazole-modified aliphatic urethane acrylate oligomer (B) include polymerization of a bifunctional aliphatic isocyanate compound (for example, hexamethylene diisocyanate, dicyclohexyl methane diisocyanate, isophorone diisocyanate, etc.). Hydroxy acrylate monomers containing up to 2 possible unsaturated groups per molecule (e.g., hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, hydroxybutyl acrylate, hydroxypentyl What was obtained by making the aliphatic urethane acrylate oligomer which is reaction product with acrylate, hydroxybutyl methacrylate, etc.) react with the benzotriazole modified acrylate which has a hydroxyl group can be used. Specific examples of the benzotriazole-modified acrylates usable in the present invention include RUVA-93 by Otsuka.

성분(B)의 합성 원료 중 벤조트리아졸 변성 아크릴레이트의 경우, 내후성, 내산화성, 특히 상용성 및 투명도를 고려하였을 때 중량평균분자량이 300~500 범위인 것이 바람직하게 사용될 수 있다. 이 분자량 범위를 벗어나는 벤조트리아졸 변성 아크릴레이트를 시용할 경우, 투명성 및 상용성이 저하될 수 있고, 도료 조성물의 변색을 유발할 수 있다. In the case of the benzotriazole-modified acrylate in the synthetic raw material of component (B), a weight average molecular weight in the range of 300 to 500 may be preferably used in consideration of weather resistance, oxidation resistance, in particular, compatibility and transparency. When benzotriazole-modified acrylate outside of this molecular weight range is applied, transparency and compatibility may be lowered and discoloration of the coating composition may be caused.

본 발명의 자외선 경화형 도료 조성물에는 상기 성분(B)가, 유기용매를 제외한 조성물 성분 총합을 기준으로, 바람직하게는 3~20 중량%가, 보다 바람직하게는 5~15 중량%가 포함된다. 조성물 내 성분(B)의 함량이, 유기용매를 제외한 조성물 성분 총합을 기준으로 3 중량% 미만이면 도막의 내후성 및 내산화성이 저하되기 쉽고, 반대로 20 중량%를 초과하면 자외선 흡수로 인한 도막의 미경화와 수지 자체의 특성으로 인한 도막의 변색이 유발될 수 있다. In the ultraviolet curable coating composition of the present invention, the component (B) is preferably 3 to 20% by weight, more preferably 5 to 15% by weight based on the total composition of the composition excluding the organic solvent. If the content of component (B) in the composition is less than 3% by weight based on the total composition of the composition excluding the organic solvent, the weather resistance and oxidation resistance of the coating film tend to be lowered. Discoloration of the coating film may be caused by curing and the characteristics of the resin itself.

(C) (C) 아크릴레이트Acrylate 모노머Monomer

본 발명의 자외선 경화형 도료 조성물에 포함되는 아크릴레이트 모노머는 중합이 가능한 불포화 그룹을 분자당 2~4개 함유하고 있는 아크릴레이트 모노머로서, 도막의 내스크래치성, 경도, 밀착성을 위해, 그리고 수지 조성물과 반응하여 경화물성을 보조하는 역할을 위해 사용하는 성분이다. The acrylate monomer included in the UV curable coating composition of the present invention is an acrylate monomer containing 2 to 4 polymerizable unsaturated groups per molecule, for the scratch resistance, hardness and adhesion of the coating film, and It is a component used for reacting and assisting hardened | cured material property.

상기 다관능성 아크릴레이트 모노머(C)로는, 예컨대, 부탄디올 디아크릴레이트, 1,6-헥산디올 디아크릴레이트, 1,6-헥산디올 디메타크릴레이트, 네오펜틸 글리콜 디아크릴레이트, 트리에틸렌글리콜 디아크릴레이트, 테트라에틸렌글리콜 디아크릴레이트, 트리프로필렌글리콜 디아크릴레이트, 트리메틸올프로판 트리아크릴레이트, 펜타에리스리톨 트리아크릴레이트, 글리세릴 프로폭시 트리아크릴레이트 등을 들 수 있으며, 이들은 단독으로 또는 2종 이상을 조합하여 사용할 수 있다.Examples of the polyfunctional acrylate monomer (C) include butanediol diacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, neopentyl glycol diacrylate, and triethylene glycol diacrylate. Acrylate, tetraethylene glycol diacrylate, tripropylene glycol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, glyceryl propoxy triacrylate, and the like. Can be used in combination.

본 발명의 자외선 경화형 도료 조성물에는 상기 성분(C)가, 유기용매를 제외한 조성물 성분 총합을 기준으로, 바람직하게는 5~40 중량%가, 보다 바람직하게는 25~35 중량%가 포함된다. 조성물 내 성분(C)의 함량이, 유기용매를 제외한 조성물 성분 총합을 기준으로 5 중량% 미만이면 도료의 점도가 상승하고 기재에의 부착성이 떨어지며, 반대로 40 중량%를 초과하면 경화성과 내스크래치성 저하, 자외선 경화시 미반응물 존재에 따라 장기적으로 도막의 백탁을 유발할 수 있다. In the ultraviolet curable coating composition of the present invention, the component (C) is preferably 5 to 40% by weight, more preferably 25 to 35% by weight based on the total composition of the composition excluding the organic solvent. If the content of component (C) in the composition is less than 5% by weight based on the total composition of the composition excluding the organic solvent, the viscosity of the paint increases and the adhesion to the substrate decreases. Degradation and UV curing can cause long-term clouding of the coating depending on the presence of unreacted materials.

(D) 광중합 개시제 ( D) photopolymerization Initiator

본 발명의 자외선 경화형 도료 조성물에 포함되는 광중합 개시제는 도막 형성 성분을 경화시키기 위해 사용되며, 예컨대, 2-하이드록시-2-메틸-1-페닐프로판-1-페논, 1-하이드록시싸이클로헥실페닐케톤, 벤조 페논, 1-(4-이소프로필페닐) 2-하이드록시 2-메틸 1-온, 1-[4-(2-하이드록시에톡시)페닐]-2-하이드록시-2-메틸 프로판 1-온, α,α-다이에톡시아세토페논, 2,2-디에톡시 1-페닐 에타논, 비스(2,4,6-트리메틸 벤조일)-페닐포스핀 옥사이드 등을 단독으로 또는 2종이상 조합하여 사용할 수 있다.The photoinitiator contained in the ultraviolet curable coating composition of the present invention is used to cure the coating film forming component, for example, 2-hydroxy-2-methyl-1-phenylpropane-1-phenone, 1-hydroxycyclohexylphenyl Ketone, benzophenone, 1- (4-isopropylphenyl) 2-hydroxy 2-methyl 1-one, 1- [4- (2-hydroxyethoxy) phenyl] -2-hydroxy-2-methyl propane 1-one, α, α-diethoxyacetophenone, 2,2-diethoxy 1-phenyl ethanone, bis (2,4,6-trimethyl benzoyl) -phenylphosphine oxide or the like alone or in combination It can be used in combination.

본 발명의 자외선 경화형 도료 조성물에는 상기 성분(D)가, 유기용매를 제외한 조성물 성분 총합을 기준으로, 바람직하게는 1~10 중량%가, 보다 바람직하게는 1~5 중량%가 포함된다. 조성물 내 성분(D)의 함량이, 유기용매를 제외한 조성물 성분 총합을 기준으로 1 중량% 미만이면 경화성 저하와 미경화로 인한 내스크래치성 및 부착성의 저하를 가져올 수 있으며, 반대로 10 중량%를 초과하면 미반응된 광중합개시제로 인한 오염, 저중합도에 의한 부착성 저하, 황변을 유발할 수 있다. In the ultraviolet curable coating composition of the present invention, the component (D) is preferably 1 to 10% by weight, more preferably 1 to 5% by weight, based on the total composition of the composition excluding the organic solvent. If the content of component (D) in the composition is less than 1% by weight, based on the total composition of the composition excluding the organic solvent, it may result in a lowering of the hardenability and a lowering of scratch resistance and adhesion due to uncuring. It may cause contamination by unreacted photopolymerization initiator, deterioration of adhesion due to low degree of polymerization, and yellowing.

(E) 자외선 흡수제(E) UV absorbers

본 발명의 자외선 경화형 도료 조성물에 포함되는 자외선 흡수제는 경화 도막의 내후성 및 플라스틱 소재의 내구성을 향상시키기 위해 사용된다. 바람직한 자외선 흡수제로는 트리아진 계열 화합물을 들 수 있으며, 구체적으로는, 이에 한정되는 것은 아니나, 6-[비스(2,4-다이메틸페닐)-1,3,5-트리아진, 6-[비스(2,4-다이메틸페닐)-1,3,5 트리아진, 트리스[2,4,6-[2-{4-(옥틸-2-메틸에타노에이트)옥시-2하이드록시페닐}]-1,3,5 트리아진 등을 단독으로 또는 2종이상 조합하여 사용할 수 있다.The ultraviolet absorber included in the ultraviolet curable coating composition of the present invention is used to improve the weather resistance of the cured coating film and the durability of the plastic material. Preferred ultraviolet absorbers include triazine-based compounds, and specific examples include, but are not limited to, 6- [bis (2,4-dimethylphenyl) -1,3,5-triazine, 6- [bis (2,4-dimethylphenyl) -1,3,5 triazine, tris [2,4,6- [2- {4- (octyl-2-methylethanoate) oxy-2hydroxyphenyl}]- 1,3,5 triazine etc. can be used individually or in combination of 2 or more types.

본 발명의 자외선 경화형 도료 조성물에는 상기 성분(E)가, 유기용매를 제외한 조성물 성분 총합을 기준으로, 바람직하게는 0.5~10 중량%가, 보다 바람직하게는 0.75~8 중량%가 포함된다. 조성물 내 성분(E)의 함량이, 유기용매를 제외한 조성물 성분 총합을 기준으로 0.5 중량% 미만이면 내후성이 저하되어 장기옥외 환경에서 도막의 열화 및 황변, 크랙 등이 유발될 수 있으며, 반대로 10 중량%를 초과하면 광경화 반응을 저하시켜 미경화 및 내수성이 취약하게 되어 백탁을 유발할 수 있다. In the ultraviolet curable coating composition of the present invention, the component (E) is preferably 0.5 to 10% by weight, more preferably 0.75 to 8% by weight based on the total composition of the composition excluding the organic solvent. If the content of the component (E) in the composition is less than 0.5 wt% based on the total composition of the composition excluding the organic solvent, the weather resistance may decrease, which may cause deterioration, yellowing, and cracking of the coating film in a long-term outdoor environment. Exceeding the% decreases the photocuring reaction, so that uncuring and water resistance are weak, which may cause cloudiness.

(F) (F) 광안정제Light stabilizer

본 발명의 자외선 경화형 도료 조성물에 포함되는 광안정제(또는 산화방지제)는 경화 도막의 내후성 및 플라스틱 소재의 내구성을 향상시키기 위해 사용된다. 바람직한 광안정제로는 힌더드아민계 광안정제(hindered amine light stabilizer, HALS)를 들 수 있으며, 구체적으로는, 이에 한정되는 것은 아니나, 비스(1-메톡시-2,2,6,6-테트라메틸-4-피페리딜)세바케이트 등을 들 수 있다. 이러한 광안정제 화합물은 단독으로 또는 2종이상 조합하여 사용할 수 있다.The light stabilizer (or antioxidant) contained in the ultraviolet curable coating composition of the present invention is used to improve the weather resistance of the cured coating film and the durability of the plastic material. Preferred light stabilizers include hindered amine light stabilizers (HALS), specifically, but not limited to, bis (1-methoxy-2,2,6,6-tetra Methyl-4-piperidyl) sebacate etc. are mentioned. These light stabilizer compounds may be used alone or in combination of two or more thereof.

본 발명의 자외선 경화형 도료 조성물에는 상기 성분(F)가, 유기용매를 제외한 조성물 성분 총합을 기준으로, 바람직하게는 0.1~5 중량%가, 보다 바람직하게는 0.2~2.5 중량%가 포함된다. 조성물 내 성분(F)의 함량이, 유기용매를 제외한 조성물 성분 총합을 기준으로 0.1 중량% 미만이면 내후성이 저하되어 장기옥외 환경에서 도막의 열화 및 황변, 크랙 등이 유발될 수 있으며, 반대로 5 중량%를 초과하면 광경화 반응을 저하시켜 미경화 및 내수성이 취약하게 되어 백탁을 유발할 수 있다. In the ultraviolet curable coating composition of the present invention, the component (F) is preferably 0.1 to 5% by weight, more preferably 0.2 to 2.5% by weight based on the total composition of the composition excluding the organic solvent. If the content of the component (F) in the composition is less than 0.1% by weight based on the total composition of the composition excluding the organic solvent, the weather resistance may deteriorate, which may cause deterioration, yellowing, and cracking of the coating film in a long-term outdoor environment. Exceeding the% decreases the photocuring reaction, so that uncuring and water resistance are weak, which may cause cloudiness.

상기 자외선 흡수제: 광안정제 사용량 비율은 중량비로 2:1 내지 4:1 이 적당하다. The amount of the ultraviolet absorber: light stabilizer used is preferably 2: 1 to 4: 1 by weight.

본 발명의 자외선 경화형 도료 조성물에는 상기한 성분들 이외에 도료 조성물에 통상적으로 첨가되는 용제, 습윤제, 레벨링제, 소포제 등이 더 포함될 수 있다. 이들 추가의 성분들은 도료의 작업성 및 도막의 평활성을 강화시킨다. In addition to the above components, the ultraviolet curable coating composition of the present invention may further include a solvent, a wetting agent, a leveling agent, an antifoaming agent, and the like, which are conventionally added to the coating composition. These additional ingredients enhance the workability of the paint and the smoothness of the coating.

본 발명에서 사용가능한 용제로는 아세톤 등의 케톤류, 에틸아세테이트 등의 아세테이트류, 또는 톨루엔 등의 방향족 화합물과 같은 통상의 용제 단독 또는 혼합물을 들 수 있다. 상기 용제를 사용하는 경우, 그 함량이 도료 조성물 총 100 중량%에 대해서 30 중량% 미만이면 작업성 및 레벨링이 떨어질 수 있고, 80 중량%를 초과하면 도막 형성이 저하되기 쉽다. 본 발명에 사용가능한 습윤제로는 폴리에테르 변성 폴리디메틸실록산을, 소포제로는 디메틸폴리실록산을, 레벨링제로는 실리콘 디아크릴레이트계나 실리콘 폴리아크릴레이트계 화합물을 들 수 있는데, 이들 각각의 사용량은 전체 도료 조성물 100 중량%에 대해서 1 중량%를 넘지 않는 것이 바람직하다.Examples of the solvent usable in the present invention include conventional solvents alone or mixtures such as ketones such as acetone, acetates such as ethyl acetate, and aromatic compounds such as toluene. In the case of using the solvent, if the content is less than 30% by weight based on 100% by weight of the coating composition, workability and leveling may be reduced, and when the content exceeds 80% by weight, coating film formation is likely to be lowered. The wetting agents usable in the present invention include polyether-modified polydimethylsiloxanes, antifoaming agents, dimethylpolysiloxanes, and leveling agents include silicone diacrylate-based and silicone polyacrylate-based compounds. It is preferable not to exceed 1% by weight relative to 100% by weight.

본 발명의 자외선 경화형 도료 조성물의 제조방법에는 특별한 제한이 없으며, 예컨대 상기한 바와 같은 성분 (A) 내지 (F)를, 필요에 따라 희석용제, 표면조절용 첨가제 등과 함께 디졸버, 교반기 등과 같은 혼합용 장비에 투입한 후, 적절한 온도(예컨대 상온)에서 혼합하는 통상의 방법에 따라 제조될 수 있다.There is no particular limitation on the method for producing the UV curable coating composition of the present invention. After entering the equipment, it can be prepared according to conventional methods of mixing at a suitable temperature (eg room temperature).

본 발명의 다른 측면에 따르면, 상기한 바와 같은 본 발명의 자외선 경화형 도료 조성물로부터 형성된 경화코팅층을 포함하는 성형품이 제공된다.According to another aspect of the present invention, there is provided a molded article comprising a cured coating layer formed from the ultraviolet curable coating composition of the present invention as described above.

본 발명의 자외선 경화형 도료 조성물이 적용가능한 성형품의 재질로는 플라스틱(예컨대 폴리카보네이트(PC))이 바람직하다. 본 발명의 바람직한 구체예에 따르면, 본 발명의 자외선 경화형 도료 조성물은 이러한 재질의 성형품 표면에 코팅되고 용제 건조된 후, 자외선 조사에 의해 경화되어 성형품 표면 보호용 하드코팅층을 형성한다. 본 발명의 자외선 경화형 도료 조성물은, 바람직하게는 자동차용 성형품에, 보다 바람직하게는 자동차 헤드램프용 PC 렌즈에 적용된다. As a material of the molded article to which the ultraviolet curable coating composition of this invention is applicable, plastic (for example, polycarbonate (PC)) is preferable. According to a preferred embodiment of the present invention, the ultraviolet curable coating composition of the present invention is coated on the surface of the molded article of such a material, and the solvent is dried, and then cured by ultraviolet irradiation to form a hard coat layer for protecting the molded article surface. The ultraviolet curable coating composition of the present invention is preferably applied to automobile molded articles, more preferably to PC lenses for automotive headlamps.

이하 본 발명을 하기 실시예에 의해 보다 구체적으로 설명한다. 그러나 이들 실시예는 본 발명의 이해를 돕기 위한 것일 뿐 이들에 의해 본 발명이 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to the following examples. However, these examples are only to aid the understanding of the present invention, and the present invention is not limited thereto.

[[ 실시예Example ]]

(1) 자외선 경화형 도료 조성물의 제조(1) Preparation of UV Curable Coating Composition

실시예Example  And 비교예Comparative example

하기 표 1 나타낸 바와 같은 조성으로 자외선 경화형 도료 조성물을 각각 제조하였다.
To the UV curable coating composition was prepared in the composition as shown in Table 1, respectively.

[표1]Table 1

Figure pat00001
Figure pat00001

Figure pat00002
Figure pat00002

(2)(2) 자외선 경화형 도료 조성물의 물성평가Evaluation of Properties of UV Curable Coating Composition

상기 실시예 및 비교예에서 각각 제조된 자외선 경화형 도료 조성물을 투명 폴리카보네이트 시편(상품명: 3022 L3, 삼양社)에 약 10 마이크론 두께(Top layer, 건조도막두께 기준)로 에어 스프레이 코팅하고, 80℃의 온도 조건에서 약 300초간 열풍 건조시켜 용매를 제거한 후 300mW/㎠의 고압 수은등으로 공기 중 약 20cm위치에서 3500mj/㎠의 에너지로 조사시켜 경화시킨 하드 코팅 시편에 대하여 하기와 같은 항목에 대한 평가를 실시하였으며, 그 결과를 하기 표 2에 나타내었다. UV curable coating compositions prepared in the above Examples and Comparative Examples were air spray coated on a transparent polycarbonate specimen (trade name: 3022 L3, Samyang Co., Ltd.) at a thickness of about 10 microns (Top layer, based on dry film thickness), and 80 ° C. After drying the solvent by hot air drying for about 300 seconds at a temperature condition of 300 mW / ㎠ and irradiated with energy of 3500mj / ㎠ at a position of about 20cm in the air with a high-pressure mercury lamp of 300mW / ㎠ to evaluate the following items for the hard coating specimen It carried out, and the results are shown in Table 2 below.

1) 부착성 시험: ASTM D3359에 의거 크로스 컷 테이프 테스트(cross cut tape test)를 시행하여 평가1) Adhesion test: evaluation by cross cut tape test according to ASTM D3359

2) 연필 경도: ISO 15184 및 JIS K 5600-5-4에 따르며 HB 이상일 것.2) Pencil Hardness: According to ISO 15184 and JIS K 5600-5-4, not less than HB.

3) 내스크래치성 시험: Steelwool 0000 grade 를 이용하여 500g의 힘을 주어 10회 rubbing후 도막 손상 확인.3) Scratch resistance test: Check the coating damage after rubbing 10 times with 500g force using Steelwool 0000 grade.

4) 내습성 시험: 시험온도 및 상대습도가 50 ± 2 ℃,98 ± 2%인 조건에서 240시간 방치 후, 꺼내어 1시간 동안 방치하여 관찰시 도막에 현저한 변색, 퇴색, 팽윤, 갈라짐, 광택저하 등이 없는지, 부착성에 이상이 없는지 평가.4) Moisture resistance test: After leaving for 240 hours at 50 ± 2 ℃, 98 ± 2% of the test temperature, and then removed for 1 hour, significant discoloration, discoloration, swelling, cracking, gloss reduction in the coating Evaluate whether there is no back and no abnormality in adhesion.

5) 내수성 시험: 시편을 수돗물(TAP WATER, 시험온도 40℃) 중에 240시간 침적시킨 후 꺼내어 AIR BLOW에 의해 표면의 수분을 제거한 다음, 상온에서 1시간 방치 후 관찰시 도막의 현저한 변색, 퇴색, 팽윤, 갈라짐, 광택저하 등이 없는지, 부착성에 이상이 없는지 평가.5) Water resistance test: The specimen was immersed in tap water (TAP WATER, test temperature 40 ℃) for 240 hours, then removed, and the surface moisture was removed by AIR BLOW. After 1 hour at room temperature, remarkable discoloration, fading, Evaluate whether there is no swelling, cracking, gloss decrease, etc., and whether the adhesion is abnormal.

6) 내열성 시험: 시험온도 (80 ± 2℃) 조건 하에서 300 시간 방치한 다음 꺼내어 실온에서 1시간 방치 후 관찰시 도막의 현저한 변색, 퇴색, 팽윤, 갈라짐, 광택저하 등이 없는지, 부착성에 이상이 없는지 평가.6) Heat resistance test: After leaving for 300 hours at the test temperature (80 ± 2 ℃) condition, taken out and left for 1 hour at room temperature, there is no noticeable discoloration, discoloration, swelling, cracking, gloss reduction, etc. Evaluate if there is.

7) 내약품성 시험: 유리세정제, 엔진오일을 개별 사용하여 3 N의 힘으로 20회 왕복한 다음 도막의 표면을 문질러 외관을 육안 조사 후, 실온에서 24시간 방치 하여 관찰시 도막의 현저한 변색, 퇴색, 팽윤, 갈라짐, 광택저하 등이 없는지, 부착성에 이상이 없는지 평가.7) Chemical resistance test: After using glass cleaner and engine oil separately, reciprocating 20 times with 3 N force, rubbing the surface of the coating film to visually inspect the appearance, and leaving it at room temperature for 24 hours to observe significant discoloration and fading of the coating film. Evaluate whether there is no swelling, cracking, glossiness deterioration, or any abnormality in adhesion.

8)내냉열 Cycle 시험: 시편을 (80 ± 2℃에서 3h 방치 → 실온 1h 방치 → -40℃에서 3h 방치 → 실온 1h 방치 → 50 ± 2℃, 95 % RH에서 7~15h)*5회 반복 후 실온에서 1시간 방치 하여 관찰시 도막의 현저한 변색, 퇴색, 팽윤, 갈라짐, 광택저하 등이 없는지, 부착성에 이상이 없는지 평가.8) Cold-resistant cycle test: test specimen (3 h at 80 ± 2 ℃ → 1 h at room temperature → 3 h at room temperature → 1 h at room temperature → 7 ~ 15 h at 50 ± 2 ℃, 95% RH) * 5 times After standing at room temperature for 1 hour, it was evaluated whether there was no noticeable discoloration, discoloration, swelling, cracking, gloss reduction, etc. of the coating film, and no abnormality in adhesion.

9) 촉진 내후성 시험: 5개의 시험 시편을 동시에 SAE J 2527에 규정하는 하기의 제논 아크로 조건으로 조사한 후 관찰시 도막의 현저한 변색[색차 (ΔE*): 3.0 이하], 퇴색, 팽윤, 갈라짐, 광택저하 등이 없는지, 부착성에 이상이 없는지 평가.9) Accelerated weathering test: Five test specimens were simultaneously examined under the conditions of the following xenon arc furnace as defined in SAE J 2527, and the discoloration of the coating film (color difference (ΔE *): 3.0 or less), fading, swelling, cracking, gloss Evaluate whether there is no degradation or the like and that there is no abnormality in adhesion.

제논 아크로 설정 조건Xenon arc furnace setting conditions

: 4000KJ/㎡ [340nm], BLACK PNL 온도- (LIGHT) 38±2 ℃ (DARK) 40분 조사(50±5 %RH), 사이클- 60분조사(50±5 %RH) 60분 미조사(95±5 %RH,표/이면 SPRAY),조사조도- 0.55±0.02W/(㎡ㆍnm) [340nm]: 4000KJ / ㎡ [340nm], BLACK PNL Temperature-(LIGHT) 38 ± 2 ℃ (DARK) 40 minutes irradiation (50 ± 5% RH), cycle-60 minutes irradiation (50 ± 5% RH) 60 minutes unirradiated ( 95 ± 5% RH, Table / Rear SPRAY), Irradiance-0.55 ± 0.02W / (㎡ · nm) [340nm]

10)내Chipping성 시험: 시험편을 시험용 비석기(GRAVELO METER : SAE J 400 규격품)에 의해 하기의 조건으로 내CHIPPING성 시험을 실시한 후, 도막의 현저한 갈라짐, 흠집 등이 없는지, 부착성에 이상이 없는지 평가.10) Chipping resistance test: After the test piece is subjected to chipping resistance test under the following conditions by a test stone machine (GRAVELO METER: SAE J 400 standard product), there is no significant cracking, scratches, etc. evaluation.

of mine ChippingChipping 성 시험 조건Sex test conditions

1) Shooting Distance: 150mm; 2) Shooting Angle:45 ° 3) Shooting Pressure: 3.0 Kgf/cm2; 4) Test Temperature: -40℃; 5) 비석: 50g (JIS Crushed gravel No 7 stone, 2.5~5mm, 350 ~ 400 개)
1) Shooting Distance: 150mm; 2) Shooting Angle: 45 ° 3) Shooting Pressure: 3.0 Kgf / cm2; 4) Test Temperature: -40 ° C; 5) Headstone: 50g (JIS Crushed gravel No 7 stone, 2.5 ~ 5mm, 350 ~ 400 pieces)

[표2][Table 2]

Figure pat00003

Figure pat00003

Claims (9)

(A) 6개 이상의 중합성 관능기를 갖는 다관능성 지방족 우레탄 아크릴레이트 올리고머, (B) 벤조트리아졸 변성 지방족 우레탄 아크릴레이트 올리고머, (C) 다관능성 아크릴레이트 모노머, (D) 광중합 개시제, (E) 자외선 흡수제 및 (F) 광안정제를 포함하는 자외선 경화형 도료 조성물.(A) a polyfunctional aliphatic urethane acrylate oligomer having six or more polymerizable functional groups, (B) benzotriazole-modified aliphatic urethane acrylate oligomer, (C) polyfunctional acrylate monomer, (D) photopolymerization initiator, (E) An ultraviolet curable coating composition comprising a ultraviolet absorber and (F) light stabilizer. 제1항에 있어서, 다관능성 지방족 우레탄 아크릴레이트 올리고머(A)가 2관능의 지방족 이소시아네이트의 화합물과 중합이 가능한 불포화 그룹을 분자당 3개 이상 함유하는 하이드록시 아크릴레이트 모노머와의 반응생성물인 것을 특징으로 하는 자외선 경화형 도료 조성물.The polyfunctional aliphatic urethane acrylate oligomer (A) is a reaction product according to claim 1, wherein the polyfunctional aliphatic urethane acrylate oligomer (A) is a reaction product with a compound of a bifunctional aliphatic isocyanate and a hydroxy acrylate monomer containing 3 or more unsaturated groups per molecule. UV curable coating composition. 제1항에 있어서, 벤조트리아졸 변성 지방족 우레탄 아크릴레이트 올리고머(B)가 2관능의 지방족 이소시아네이트의 화합물과 중합이 가능한 불포화 그룹을 분자당 2개 이하로 함유하는 하이드록시 아크릴레이트 모노머와의 반응생성물인 지방족 우레탄 아크릴레이트 올리고머를 벤조트리아졸 변성 아크릴레이트와 반응시켜 얻어진 것임을 특징으로 하는 자외선 경화형 도료 조성물.The reaction product according to claim 1, wherein the benzotriazole-modified aliphatic urethane acrylate oligomer (B) is a reaction product with a compound of bifunctional aliphatic isocyanate and a hydroxy acrylate monomer containing not more than two unsaturated groups per molecule. An ultraviolet curable coating composition obtained by reacting a phosphorus aliphatic urethane acrylate oligomer with a benzotriazole-modified acrylate. 제1항에 있어서, 다관능성 아크릴레이트 모노머(C)가 부탄디올 디아크릴레이트, 1,6-헥산디올 디아크릴레이트, 1,6-헥산디올 디메타크릴레이트, 네오펜틸 글리콜 디아크릴레이트, 테트라글리콜 디아크릴레이트, 트리프로필렌글리콜 디아크릴레이트, 폴리에틸렌글리콜 디아크릴레이트, 트리메틸올프로판 메타크릴레이트, 프로폭시레이티드 트리메틸올프로판 트리아크릴레이트, 프로폭시레이티드 트리메틸올프로판 트리메타크릴레이트, 트리메틸올프로판 트리메타크릴레이트, 펜타에리뜨리톨 트리아크릴레이트, 글리세릴 프로폭시 트리아크릴레이트, 트리스 이소시아누레이트 트리아크릴레이트 또는 이들의 혼합물인 것을 특징으로 하는 자외선 경화형 도료 조성물.The polyfunctional acrylate monomer (C) according to claim 1, wherein the polyfunctional acrylate monomer (C) is butanediol diacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, neopentyl glycol diacrylate, tetraglycol. Diacrylate, tripropylene glycol diacrylate, polyethylene glycol diacrylate, trimethylolpropane methacrylate, propoxylated trimethylolpropane triacrylate, propoxylated trimethylolpropane trimethacrylate, trimethylolpropane It is trimethacrylate, pentaerythritol triacrylate, glyceryl propoxy triacrylate, tris isocyanurate triacrylate, or a mixture thereof, The ultraviolet curable coating composition characterized by the above-mentioned. 제1항에 있어서, 자외선 흡수제(E)가 트리아진 계열 화합물인 것을 특징으로 하는 자외선 경화형 도료 조성물.The ultraviolet curable coating composition according to claim 1, wherein the ultraviolet absorbent (E) is a triazine-based compound. 제1항에 있어서, 광안정제(F)가 힌더드아민계 광안정제인 것을 특징으로 하는 자외선 경화형 도료 조성물.The ultraviolet curable coating composition according to claim 1, wherein the light stabilizer (F) is a hindered amine light stabilizer. 제1항 내지 제6항 중 어느 한 항에 따른 자외선 경화형 도료 조성물로부터 형성된 경화코팅층을 포함하는 성형품.A molded article comprising a cured coating layer formed from the ultraviolet curable coating composition according to any one of claims 1 to 6. 제7항에 있어서, 폴리카보네이트 재질인 것을 특징으로 하는 성형품.8. The molded article of claim 7, wherein the molded article is made of polycarbonate. 제8항에 있어서, 자동차 헤드램프용 폴리카보네이트 렌즈인 것을 특징으로 하는 성형품.The molded article according to claim 8, which is a polycarbonate lens for an automobile headlamp.
KR1020110017277A 2011-02-25 2011-02-25 Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same KR101210905B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020110017277A KR101210905B1 (en) 2011-02-25 2011-02-25 Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020110017277A KR101210905B1 (en) 2011-02-25 2011-02-25 Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same

Publications (2)

Publication Number Publication Date
KR20120097817A true KR20120097817A (en) 2012-09-05
KR101210905B1 KR101210905B1 (en) 2012-12-11

Family

ID=47108970

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020110017277A KR101210905B1 (en) 2011-02-25 2011-02-25 Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same

Country Status (1)

Country Link
KR (1) KR101210905B1 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104098941A (en) * 2014-08-05 2014-10-15 张家港康得新光电材料有限公司 Hard coating material as well as preparation method and use thereof
KR101465027B1 (en) * 2013-02-22 2014-11-26 호서대학교 산학협력단 Coating composition for plastic shield part of vehicle head lamp
KR20150021855A (en) * 2013-08-21 2015-03-03 현대모비스 주식회사 Uv-curable composition for hard-coat paining
CN104419316A (en) * 2013-08-21 2015-03-18 现代摩比斯株式会社 Uv-curable composition for hard-coat paining
KR101517192B1 (en) * 2014-01-24 2015-05-12 주식회사 케이씨씨 Uv-curable coating composition and molded article comprisng a cured coating layer formed from the same
KR20160095647A (en) * 2016-07-11 2016-08-11 현대모비스 주식회사 Uv-curable composition for hard-coat paining
WO2017125339A1 (en) * 2016-01-21 2017-07-27 Basf Coatings Gmbh Radiation-curable coating agent, method for creating scratch-resistant coatings, use of the coating agent, and substrate coated with a coating agent
US9938427B2 (en) 2013-05-31 2018-04-10 Kcc Corporation Radiation curable paint composition and molded product comprising cured coating layer formed therefrom
KR20190019305A (en) * 2017-08-17 2019-02-27 현대모비스 주식회사 A composition for hard-coat painting having excellent light resistance with high hardness

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101423193B1 (en) 2013-04-09 2014-07-25 주식회사 노루비케미칼 Uv-curable coating composition for flow coating and flow coating method for using the same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5365038B2 (en) 2007-06-19 2013-12-11 住友ベークライト株式会社 UV curable paint, hard coat layer, transparent polycarbonate sheet

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101465027B1 (en) * 2013-02-22 2014-11-26 호서대학교 산학협력단 Coating composition for plastic shield part of vehicle head lamp
US9938427B2 (en) 2013-05-31 2018-04-10 Kcc Corporation Radiation curable paint composition and molded product comprising cured coating layer formed therefrom
KR20150021855A (en) * 2013-08-21 2015-03-03 현대모비스 주식회사 Uv-curable composition for hard-coat paining
CN104419316A (en) * 2013-08-21 2015-03-18 现代摩比斯株式会社 Uv-curable composition for hard-coat paining
CN104419317A (en) * 2013-08-21 2015-03-18 现代摩比斯株式会社 Uv-curable composition for hard-coat painting
KR101517192B1 (en) * 2014-01-24 2015-05-12 주식회사 케이씨씨 Uv-curable coating composition and molded article comprisng a cured coating layer formed from the same
CN104098941A (en) * 2014-08-05 2014-10-15 张家港康得新光电材料有限公司 Hard coating material as well as preparation method and use thereof
WO2017125339A1 (en) * 2016-01-21 2017-07-27 Basf Coatings Gmbh Radiation-curable coating agent, method for creating scratch-resistant coatings, use of the coating agent, and substrate coated with a coating agent
CN108473793A (en) * 2016-01-21 2018-08-31 巴斯夫涂料有限公司 Radiation-curable coating, method, the purposes of coating and the base material coated with coating for generating scratch resistance coating
CN108473793B (en) * 2016-01-21 2020-05-12 巴斯夫涂料有限公司 Radiation-curable coating, method for producing a scratch-resistant coating, use of a coating and substrate coated with a coating
KR20160095647A (en) * 2016-07-11 2016-08-11 현대모비스 주식회사 Uv-curable composition for hard-coat paining
KR20190019305A (en) * 2017-08-17 2019-02-27 현대모비스 주식회사 A composition for hard-coat painting having excellent light resistance with high hardness

Also Published As

Publication number Publication date
KR101210905B1 (en) 2012-12-11

Similar Documents

Publication Publication Date Title
KR101210905B1 (en) Uv-curable coating composition useful as top surface coating for plastic substrate and molded article comprisng a cured coating layer formed from the same
KR101127932B1 (en) Resin and composition for ultraviolet curable coating and automobile head lamp lens comprising a coating layer thereof
US20220169889A1 (en) UV Curable Coating Compositions Containing Aliphatic Urethane Acrylate Resins
KR102282639B1 (en) Radiation curable hardcoat with improved weatherability
TWI450939B (en) Coating composition for coating onto plastic base material, coating film formed from the same, and coated products thereof
US9938427B2 (en) Radiation curable paint composition and molded product comprising cured coating layer formed therefrom
JP5283485B2 (en) Active energy ray-curable composition and molded article having a cured coating of the composition
KR102036100B1 (en) Uv-curable composition for hard-coat paining
JP5343014B2 (en) Active energy ray-curable coating composition and molded article having a cured film of the composition
JP6354665B2 (en) Photocurable coating composition and coated article
JP2007314770A (en) Active energy ray-curable coating composition, and molded article having cured film of the composition
JP6515806B2 (en) Active energy ray-curable resin composition, resin molded article and method for producing resin molded article
KR20150021854A (en) Uv-curable composition for hard-coat paining
JP5075508B2 (en) Compound suitable for light stabilizer and active energy ray-curable composition containing the same
JP6451627B2 (en) Active energy ray-curable resin composition and automobile headlamp lens
KR101684995B1 (en) Uv-curable composition for hard-coat paining
KR101755101B1 (en) Surface protecting uv-curable coating composition
KR102190088B1 (en) Radiation-curable coating agent, method of manufacturing scratch-resistant coating, use of coating agent, and substrate coated with coating agent

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20151012

Year of fee payment: 6

FPAY Annual fee payment

Payment date: 20181126

Year of fee payment: 9