KR100413852B1 - One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same - Google Patents

One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same Download PDF

Info

Publication number
KR100413852B1
KR100413852B1 KR10-2000-0087440A KR20000087440A KR100413852B1 KR 100413852 B1 KR100413852 B1 KR 100413852B1 KR 20000087440 A KR20000087440 A KR 20000087440A KR 100413852 B1 KR100413852 B1 KR 100413852B1
Authority
KR
South Korea
Prior art keywords
weight
silicone
resin
curing agent
parts
Prior art date
Application number
KR10-2000-0087440A
Other languages
Korean (ko)
Other versions
KR20020059059A (en
Inventor
김재학
Original Assignee
주식회사 디피아이
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 디피아이 filed Critical 주식회사 디피아이
Priority to KR10-2000-0087440A priority Critical patent/KR100413852B1/en
Publication of KR20020059059A publication Critical patent/KR20020059059A/en
Application granted granted Critical
Publication of KR100413852B1 publication Critical patent/KR100413852B1/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
    • C09D183/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04Polysiloxanes
    • 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
    • C08K5/01Hydrocarbons
    • 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
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08L61/28Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L87/00Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
    • C08L87/005Block or graft polymers not provided for in groups C08L1/00 - C08L85/04
    • 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • 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
    • C09D7/20Diluents or solvents
    • 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
    • C09D7/45Anti-settling agents
    • 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
    • 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
    • C09D7/80Processes for incorporating ingredients

Abstract

고내후성, 고경도, 내스크레치성을 갖는 1액형 실리콘 변성 아크릴계 도료 조성물 및 이의 제조방법이 개시되어 있다. 상기 실리콘 변성 아크릴계 도료 조성물은 산가 5 내지 15, 알코올가 30 내지 100, 중량평균분자량 15,000 내지 30,000, 불휘발분 40내지 70%, 유리전이온도 30 내지 70℃의 특성치를 갖는 실리콘 변성 아크릴수지 35 내지 65중량부, 제1 경화제로서 멜라민 수지를 8 내지 18중량부 및 제2 경화제로서 블록이소시아네이트 수지를 0.6 내지 3.0중량부를 포함한다. 본 발명의 도료 조성물은 도장전에 주제와 경화제를 혼합해야 하는 과정이 필요 없고 저장성에 문제가 없으며 고내후성, 고경도, 내오염성, 내스크레치성, 내약품성 등의 우수한 물성을 갖는다.Disclosed is a one-component silicone-modified acrylic coating composition having high weather resistance, high hardness, and scratch resistance, and a method of manufacturing the same. The silicone modified acrylic coating composition has an acid value of 5 to 15, an alcohol value of 30 to 100, a weight average molecular weight of 15,000 to 30,000, a nonvolatile content of 40 to 70%, and a silicone modified acrylic resin of 35 to 65 weight having a glass transition temperature of 30 to 70 ° C. It contains 8-18 weight part of melamine resin as a 1st hardening | curing agent, and 0.6-3.0 weight part of block isocyanate resins as a 2nd hardening | curing agent. The coating composition of the present invention does not require the process of mixing the main agent and the curing agent before coating, and there is no problem in storage properties, and has excellent physical properties such as high weather resistance, high hardness, stain resistance, scratch resistance, and chemical resistance.

Description

1액형 실리콘 변성 아크릴계 도료 조성물 및 이의 제조방법{One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same}One-liquid type silicon-modified and acryl-based paint composition and method of preparing the same

본 발명은 건축용 외장재에 도장되는 고내후성, 고경도, 내스크레치성,고광택, 내오염성, 내약품성 등의 우수한 도막물성을 갖는 가열건조형 1액형 실리콘 변성 아크릴계 도료 조성물 및 이의 제조방법에 관한 것이다.The present invention relates to a heat-dried one-component silicone-modified acrylic coating composition having excellent coating properties such as high weather resistance, high hardness, scratch resistance, high gloss, stain resistance, chemical resistance, and the like, which is coated on a building exterior material.

알루미늄판과 아연도강판을 소재로 제조되는 건축외장재 (외부 벽체판넬, 창문틀, 도어, 지붕재, 가드레일, 샷시등)의 외장재로서는 주로 내후성이 우수한 불소 도료가 사용되고 있는데, 가격이 고가인 관계로 범용적으로 사용되기는 곤란하다. 이에 대처하기 위해 물성면에서 불소 도료와 유사하면서 가격 경쟁력을 갖춘 고기능성 세라믹도료가 개발되었고 그 대표적인 것이 아크릴실리콘계 도료이다.As exterior materials for building exterior materials (outer wall panels, window frames, doors, roofing materials, guard rails, sashes, etc.) made of aluminum and galvanized steel, fluorine paint with excellent weather resistance is used. It is difficult to use universally. In order to cope with this, a high-performance ceramic paint similar to the fluorine paint in terms of physical properties and price competitiveness has been developed, and an acrylic silicone paint is a representative one.

종래의 아크릴실리콘계 도료 조성물은 구성 성분의 화학적 구조로 인한 저장성 문제로 주제와 경화제를 분리한 2액형 타입으로 사용되고 있다. 이에 따라, 도장작업시 주제와 경화제를 혼합해야 하는 번거로움과 일단 혼합하면 가사 시간 때문에 일정시간내에 도료를 소진해야하고, 남은 도료는 폐기해야만 한다는 단점이있다.Conventional acrylic silicone paint compositions have been used in a two-part type that separates the main agent and the curing agent due to storage problems due to the chemical structure of the components. Accordingly, there is a disadvantage in that the paint has to be exhausted within a certain time due to the pot life, and the remaining paint must be discarded once it is mixed with the hassle of mixing the main agent and the curing agent during painting.

종래의 2액형 아크릴실리콘계 도료의 반응 메카니즘을 살펴보면, 주제에 사용되는 아크릴수지의 백본에 있는 하이드록실기와 글리시딜기가 경화제로 사용되는 아민계 실란(예; γ-aminopropyltrimethoxysilane)과 반응하여 실록산 결합(-Si-O-Si-O-) 및 가교결합으로 망상 구조를 이루어 불소 도료의 도막 물성에 버금가는 특성을 나타낸다. 그러나, 이러한 반응 메카니즘을 갖는 도료 조성물은 공기중의 습도에 매우 민감하여 상대습도 90% 이상에서는 도막의 균열, 흡광에 의한 광택 저하등의 도막 불량 현상이 나타나는 문제가 있다. 이러한 문제점을 해결하기 위해 (주)디피아이에서는 주제와 경화제의 관능기를 바꾸어 도입하는 방법 즉, 주제의 아크릴수지 백본에 아미노기를 갖는 아크릴모노머(예; n-Butoxymethylacrylamide)와 산을 도입하고 경화제로서 글리시딜기를 갖는 실란((주)디피아이 상품명; 실락)을 사용하여 상대습도 90% 이상에서도 도막 물성에 이상이 없는 도료 조성물을 발명하여 이를 특허 출원한 바 있다. (대한민국 특허출원번호 제95-16615)Looking at the reaction mechanism of the conventional two-component acrylic silicone paint, a siloxane bond is formed by reacting with an amine silane (e.g., γ-aminopropyltrimethoxysilane) in which the hydroxyl group and glycidyl group in the backbone of the acrylic resin used in the subject are used as curing agents. (-Si-O-Si-O-) and cross-linked to form a network structure exhibits properties comparable to the physical properties of fluorine paint. However, the coating composition having such a reaction mechanism is very sensitive to the humidity in the air, and there is a problem in that a coating film defect phenomenon such as cracking of the coating film and gloss reduction due to absorption occurs at a relative humidity of 90% or more. In order to solve this problem, DIPAI Co., Ltd. introduces alternating functional groups of main body and curing agent, that is, acryl monomer (eg n-Butoxymethylacrylamide) and acid having amino group in main acrylic resin backbone, and Glyci as a curing agent. Using a silane having a dill group (Dipia Co., Ltd. trade name; silane), the invention has been applied for a coating composition having no abnormality in coating properties even at a relative humidity of 90% or more. (Korean Patent Application No. 95-16615)

그러나, 이러한 2액형 아크릴실리콘계 도료 조성물은 도막 물성면에서는 불소 도료에 버금가는 우수한 특성을 나타내지만, 가사 시간이 24시간이내이기 때문에 도장 작업에 제약이 따르는 문제는 여전히 남아 있어 1액형 타입 도료 조성물의 필요성이 지속적으로 요구되고 있다.However, although the two-component acrylic silicone paint composition exhibits excellent properties comparable to fluorine paint in terms of coating film properties, the potting time is within 24 hours. The need continues to be demanded.

본 발명에서는 아크릴실리콘계 도료 조성물의 1액형화를 위한 저장성문제를 해결하여 저장성에 문제가 없고, 아크릴실리콘계 도료의 특성인 고내후성, 고경도,내오염성, 내스크레치성, 내약품성 등의 우수한 물성을 갖는 실리콘 변성 아크릴수지/멜라민/블록이소시아네이트 시스템으로 구성된 1액형 도료 조성물을 제공하는 것을 그 목적으로 한다.In the present invention, there is no problem in storage properties by solving the storage problem for the one-component conversion of the acrylic silicone paint composition, and excellent properties such as high weather resistance, high hardness, stain resistance, scratch resistance, chemical resistance, etc. It is an object to provide a one-part coating composition composed of a silicone-modified acrylic resin / melamine / block isocyanate system having.

본 발명의 다른 목적은 상기한 도료 조성물의 용이한 제조 방법을 제공하는 것이다.Another object of the present invention is to provide an easy method for producing the coating composition described above.

상기한 목적을 달성하기 위하여 본 발명에서는In the present invention to achieve the above object

산가 5 내지 15, 알코올가 30 내지 100, 중량평균분자량 15,000 내지 30,000, 불휘발분 40 내지 70%, 유리전이온도 30 내지 70℃의 특성치를 갖는 실리콘 변성 아크릴수지 35 내지 65중량부;35 to 65 parts by weight of a silicone-modified acrylic resin having a characteristic value of 5 to 15 acid, 30 to 100 alcohol, 15,000 to 30,000 weight average molecular weight, 40 to 70% nonvolatile content, and 30 to 70 ° C glass transition temperature;

제1 경화제로서 멜라민 수지를 8 내지 18중량부; 및8 to 18 parts by weight of the melamine resin as the first curing agent; And

제2 경화제로서 블록이소시아네이트 수지를 0.6 내지 3.0중량부를 포함하는 1액형 실리콘 변성 아크릴계 도료 조성물을 제공한다.Provided is a one-part silicone-modified acrylic coating composition containing 0.6 to 3.0 parts by weight of a block isocyanate resin as a second curing agent.

특히, 상기 멜라민 수지가 메톡시메칠 및 메톡시메칠-이미노 관능기를 갖는 수지이고 상기 블록이소시아네이트 수지가 헥사메칠렌디이소시아네이트타입의 수지인 것이 바람직하다.In particular, it is preferable that the said melamine resin is resin which has a methoxymethyl and a methoxymethyl- imino functional group, and the said block isocyanate resin is a hexamethylene diisocyanate type resin.

상기한 본 발명의 다른 목적은Another object of the present invention described above

40 내지 60 중량부의 아크릴 단량체, 15 내지 35 중량부의 용제 및 반응 개시제를 혼합하여 하이드록시기를 포함하며 알코올가가 70 내지 170 범위인 아크릴 수지를 제조하는 단계;Mixing 40 to 60 parts by weight of an acrylic monomer, 15 to 35 parts by weight of a solvent and a reaction initiator to prepare an acrylic resin containing a hydroxyl group and having an alcohol value in the range of 70 to 170;

얻어지는 아크릴 수지와 5 내지 20 중량부의 하이드록시기 또는 메톡시기를 갖는 실리콘 중간체를 탈수 반응시켜 실록산 결합을 갖는 실리콘 변성 아크릴 수지를 제조하는 단계; 및Dehydrating the obtained acrylic resin with a silicone intermediate having 5 to 20 parts by weight of a hydroxyl group or a methoxy group to prepare a silicone-modified acrylic resin having a siloxane bond; And

상기 실리콘 변성 아크릴 수지에 제1 경화제인 멜라민 수지 및 제2 경화제인 블록이소시아네이트 수지를 첨가하는 단계를 포함하는 1액형 실리콘 변성 아크릴계 도료 조성물의 제조 방법에 의해 달성된다.It is achieved by a method for producing a one-component silicone modified acrylic coating composition comprising the step of adding a melamine resin as a first curing agent and a block isocyanate resin as a second curing agent to the silicone-modified acrylic resin.

특히, 상기 실리콘 중간체는 분자량이 500∼3,000 이고 규소 함량이 3∼20% 범위에 있는 것이 바람직하게 사용될 수 있으며, 상기 경화제의 첨가시 방향족계 설폰산 또는 인산계 반응 촉매를 0.1∼3 중량부 더 첨가하는 것이 또한 바람직하다.In particular, the silicon intermediate may preferably be used having a molecular weight of 500 to 3,000 and a silicon content in the range of 3 to 20%, and 0.1 to 3 parts by weight of an aromatic sulfonic acid or phosphoric acid reaction catalyst upon addition of the curing agent. It is also preferred to add.

이하, 본 발명을 보다 상세히 설명하기로 한다.Hereinafter, the present invention will be described in more detail.

주체 수지인 실리콘 변성 아크릴수지는 1차 반응을 통해 하이드록실기를 포함하며 아크릭 백본 구조를 갖는 아크릴 수지를 제조한 후, 하이드록시기 또는 메톡시기를 갖는 실리콘 중간체와의 2차 반응을 통해 실록산결합(-Si-O-Si-O-)을 갖도록 하는 방식으로 제조하였다. 2차 반응에서 사용되는 실리콘 중간체는 총중량 대비 5 내지 20 중량부 범위내에서 사용하였다.The silicone-modified acrylic resin, which is a main resin, contains a hydroxyl group through a first reaction, and prepares an acrylic resin having an aric backbone structure, and then bonds a siloxane through a secondary reaction with a silicon intermediate having a hydroxyl group or a methoxy group. It was prepared in such a way as to have (-Si-O-Si-O-). The silicon intermediate used in the secondary reaction was used within the range of 5 to 20 parts by weight relative to the total weight.

1차 반응에서 일반적으로 많이 사용하는 아크릴 단량체를 이용하여 알코올가가 70 내지 170 범위에 들도록하여 아크릴 수지를 합성하고 있는데, 일반적인 아크릴 단량체로는 메틸메타크릴레이트, 메틸아크릴레이트, 에틸아크릴레이트, 스티렌, 2-에틸헥실아크릴레이트, 노말-부틸 아크릴레이트, 2-하이드록시에틸 메타크릴레이트, 2-하이드록시에틸 아크릴레이트, 메타크릴산, 아크릴산 등을 사용할 수 있다.The acrylic resin is synthesized by using the acrylic monomer commonly used in the first reaction so that the alcohol value is in the range of 70 to 170. As the general acrylic monomer, methyl methacrylate, methyl acrylate, ethyl acrylate, styrene, 2-ethylhexyl acrylate, normal-butyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, methacrylic acid, acrylic acid and the like can be used.

2차 반응에 투입되는 하이드록시기를 함유하는 실리콘 중간체로는 Dow Corning사(미국)의 Z-6018(상품명) 수지와 Chisso(미국)사의 FM-4411(상품명) 수지를 사용할 수 있으며, 메톡시기를 함유하는 실리콘 중간체로는 Shin-Etsu사(일본)의 KR-9218(상품명) 수지와 Toshiba(일본)사의 TRS-165(상품명) 수지를 사용할 수 있다.Silicone intermediates containing a hydroxyl group added to the secondary reaction may be Z-6018 (trade name) resin of Dow Corning (USA) and FM-4411 (trade name) resin of Chisso (USA). As the silicone intermediate to be contained, KR-9218 (trade name) resin of Shin-Etsu (Japan) and TRS-165 (trade name) resin of Toshiba (Japan) can be used.

이하, 본 발명에 따른 도료 조성물의 제조 방법을 좀 더 상세히 설명하기로 한다.Hereinafter, the manufacturing method of the coating composition according to the present invention will be described in more detail.

먼저 크실렌, 셀루솔브아세테이트, 코코졸-100과 같은 고비점 용제를 단독 또는 혼합액으로 선택하여 15 내지 35 중량부를 합성플라스크에 넣고 130 내지 150℃로 승온한다. 여기에, 선택된 아크릴 단량체 40 내지 60 중량부와 벤조일퍼옥사이드, t-부틸 퍼옥시옥토에이트와 같은 유기과산화물계 라디칼 개시제 0.5 내지 2.0 중량부의 혼합물을 2 내지 5시간에 걸쳐 균일속도로 적하한다.First, high boiling point solvents such as xylene, cellulose acetate, and cocosol-100 are selected alone or as a mixed solution, and 15 to 35 parts by weight are put in a synthetic flask and heated to 130 to 150 ° C. Here, a mixture of 40 to 60 parts by weight of the selected acrylic monomer and 0.5 to 2.0 parts by weight of an organic peroxide radical initiator such as benzoyl peroxide and t-butyl peroxyoctoate is added dropwise at a uniform rate over 2 to 5 hours.

적하 후 30분 내지 60분 동안 유지반응한 후 유기과산화물 개시제 0.1 내지 0.4 중량부를 1회 내지 3회에 걸쳐 투입하고 60분 내지 120분 동안 유지반응시킨다.After dropping, the reaction was carried out for 30 to 60 minutes, and then 0.1 to 0.4 parts by weight of the organic peroxide initiator was added once to three times, followed by the holding reaction for 60 to 120 minutes.

유지반응 후 반응촉진제로서 테트라 이소프로필 티타네이트, 테트라 부틸 티타네이트와 같은 유기 티탄계 화합물 0.05∼0.1 중량부와 실리콘 중간체 5∼20 중량부, 톨루엔 5∼10 중량부를 넣고 90∼150분에 걸쳐 탈수반응을 진행하여 실리콘 변성 아크릴 수지를 제조하도록 한다.After the fat and oil reaction, 0.05 to 0.1 parts by weight of an organic titanium compound such as tetra isopropyl titanate and tetra butyl titanate, 5 to 20 parts by weight of silicon intermediate, and 5 to 10 parts by weight of toluene were added and dehydrated over 90 to 150 minutes. The reaction is carried out to produce a silicone-modified acrylic resin.

2차 반응에서 사용된 톨루엔은 반응시 발생되는 물을 제거하기 위한 순회(Reflux) 용제로 사용되는 것이며, 최종 결과물에는 포함되지 않는다. 이러한 실리콘 중간체와의 반응을 통하여 산가 5 내지 15, 알코올가 30 내지 100, 중량평균분자량 15,000 내지 30,000, 불휘발분 40 내지 70%, 유리전이온도 30 내지 70℃의 특성치를 갖는 실리콘 변성 아크릴수지를 제조하도록 한다.Toluene used in the secondary reaction is used as a reflux solvent to remove water generated in the reaction and is not included in the final result. Through the reaction with the silicon intermediate to produce a silicone-modified acrylic resin having a characteristic value of 5 to 15 acid, 30 to 100 alcohol, 15,000 to 30,000 weight average molecular weight, 40 to 70% nonvolatile content, 30 to 70 ℃ glass transition temperature. do.

상술한 방법에 따라 실리콘 변성 아크릴 수지를 제조하였는데, 사용된 원료 및 이의 첨가량, 얻어지는 실리콘 변성 아크릴 수지의 물성 등에 대한 결과는 아래의 표1에 나타내었다. 각 원료의 첨가량에 대한 단위는 중량부이다.A silicone-modified acrylic resin was prepared according to the above-described method, and the results on the raw materials used and the amount thereof added, the physical properties of the silicone-modified acrylic resin obtained, and the like are shown in Table 1 below. The unit with respect to the addition amount of each raw material is a weight part.

합성 수지Synthetic resin 수지 IResin I 수지 IIResin II 수지 IIIResin III 크실렌셀루솔브아세테이트코코졸-100메틸 메타크릴레이트스티렌2-에틸헥실아크릴레이트이소부틸메타크릴레이트에틸헥실메타크릴레이트2-하이드록시에틸메타크릴레이트메틸 메타크릴산t-부틸퍼옥시옥토에이트크실렌t-부틸퍼옥시옥토에이트벤조일퍼옥사이드테트라이소프로필티타네이트Z-6018FM-4411톨루엔Xylene Cellulose Acetate Cosol-100methyl methacrylate styrene 2-ethylhexyl acrylate isobutyl methacrylate ethylhexyl methacrylate 2-hydroxyethyl methacrylate methyl methacrylate t-butylperoxy octoate xylene t Butyl peroxy octoate benzoyl peroxide tetraisopropyl titanate Z-6018FM-4411 toluene 151011.452262--9.50.5250.2-0.110-10151011.452262--9.50.5250.2-0.110-10 2515-255--12.5100.751.755-0.150.15-7.352515-255--12.5100.751.755-0.150.15-7.35 2015-30--12.5-50.51.2550.15-0.1-2.57.252015-30--12.5-50.51.2550.15-0.1-2.57.25 합계Sum 103.75103.75 107.5107.5 99.2599.25 불휘발분(%)점도(가드너)알코올가(OH 값)Nonvolatile matter (%) Viscosity (Gardner) Alcohol value (OH value) 58.5W-4058.5W-40 50.0U+5950.0U + 59 53X-4353X-43

제조된 실리콘 변성 아크릴 수지 35 내지 65 중량부에 제1 경화제 8 내지 18 중량부 및 제2 경화제 0.3 내지 3 중량부를 첨가하여 1액형 수지를 제조하도록 한다.8 to 18 parts by weight of the first curing agent and 0.3 to 3 parts by weight of the second curing agent are added to 35 to 65 parts by weight of the silicone-modified acrylic resin thus prepared to prepare a one-component resin.

상기 실리콘 변성 아크릴 수지의 첨가량이 35 중량부 보다 적으면 내후성저하 및 고온건조시 황변성이 발생하여 바람직하지 못하고, 65 중량부를 초과하면 적절한 도료의 불휘발분 및 도장작업성을 조절하기가 어려워 바람직하지 못하므로 이의 사용량은 상기한 범위가 되도록 한다.When the amount of the silicone-modified acrylic resin is less than 35 parts by weight, it is not preferable to reduce weather resistance and yellowing during high temperature drying, and when the amount of the silicone-modified acrylic resin exceeds 65 parts by weight, it is difficult to control the non-volatile content and coating workability of appropriate paints Therefore, its amount is to be in the above range.

제1 경화제로는 멜라민수지를 사용하였는데, 메톡시메칠 및 메톡시메칠-이미노 관능기를 갖는 것이 바람직하다. 구체적으로는 Cyanamid사(미국) 제품 Cymel303, 327, 325를 이용하였다.Although melamine resin was used as a 1st hardening | curing agent, what has a methoxymethyl and a methoxymethyl- imino functional group is preferable. Specifically, Cyyana303, 327, 325 manufactured by Cyanamid (USA) was used.

제1 경화제의 사용량은 8 내지 18 중량부가 되도록 하는데, 만약 이의 사용량이 8 중량부 보다 적으면 가교밀도가 저하로 스크레치성, 약품성, 경도가 약화되어 바람직하지 못하고, 18 중량부 보다 많으면 과다한 가교밀도로 도막의 깨짐성 증가로 충격성이 저하되고, 저장안정성도 떨어져 바람직하지 못하다.The amount of the first curing agent is 8 to 18 parts by weight. If the amount of the first curing agent is less than 8 parts by weight, the crosslinking density decreases, which is not preferable because the scratchability, chemical property, and hardness are weakened. The impact resistance is lowered due to the increased cracking property of the coating film, and the storage stability is also unfavorable.

상기한 표 1의 방법에 따라 제조된 실리콘 변성 아크릴 수지와의 혼합 비율은 불휘발분 대비로 하여 6/4, 7/3, 8/2 비율(실리콘변성아크릴수지/멜라민수지)로 적용하였다. 실리콘 변성 아크릴수지/멜라민수지 시스템에 의하여 경화시키면 도막 성질의 경질화가 나타나 내충격성과 내굴곡성에 취약한 물성을 나타낸다.The mixing ratio with the silicone-modified acrylic resin prepared according to the method of Table 1 above was applied in a ratio of 6/4, 7/3, and 8/2 (silicone-modified acrylic resin / melamine resin) relative to the nonvolatile content. Curing with a silicone modified acrylic resin / melamine resin system results in hardening of the coating properties, indicating physical properties that are vulnerable to impact resistance and flex resistance.

따라서 이를 보완하기 위하여 제2 경화제로서 블록이소시아네이트를 도입하도록 한다. 이는 헥사메틸렌디이소시아네이트 타입이 바람직하다. 구체적으로는 Bayer사(독일) 제품 Desmodur-3175를 이용하였다. 블록이소시아네이트의 사용량은 저장성을 고려하여 실리콘 변성 아크릴수지/멜라민수지 총중량대비 0.6∼3 중량부 범위가 되도록 하였다. 제2 경화제의 첨가량이 0.6 중량부 보다 적으면 도막의 유연성 부족으로 충격성이 저하되어 바람직하지 못하며 3 중량부 보다 많으면 저장안정성이 저하되어 바람직하지 못하므로 이의 첨가량은 상기한 범위가 되도록 한다.Therefore, to compensate for this, a block isocyanate is introduced as a second curing agent. It is preferable for the hexamethylene diisocyanate type. Specifically, Desmodur-3175 manufactured by Bayer (Germany) was used. The amount of the block isocyanate is in the range of 0.6 to 3 parts by weight based on the total weight of the silicone-modified acrylic resin / melamine resin in consideration of storage properties. If the amount of the second curing agent is less than 0.6 parts by weight, the impact resistance is lowered due to lack of flexibility of the coating film, and if it is more than 3 parts by weight, the storage stability is lowered, which is not preferable.

가열경화시 원활한 반응진행을 위해 반응촉매로 강산성의 방향족계 설폰산 또는 인산계 화합물을 0.1∼3 중량부 사용하도록 한다.In order to proceed smoothly during heat curing, 0.1 to 3 parts by weight of strongly acidic aromatic sulfonic acid or phosphoric acid compound is used as a reaction catalyst.

아래의 표 2에서는 이상에서 살펴본 주체 수지인 실리콘 변성 아크릴수지와 경화제로 사용되는 멜라민수지 및 블록이소시아네이트 수지를 사용하여 1액형 도료로 제조시 각 성분의 종류 및 함량을 나타내었다. 표에서 단위는 중량부이다.Table 2 below shows the type and content of each component when prepared as a one-part coating material using a silicone-modified acrylic resin, a main resin, and a melamine resin and a block isocyanate resin used as a curing agent. Units in the table are parts by weight.

실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 유기 용제Organic solvents 8.338.33 8.338.33 8.338.33 수지 I수지 II수지 IIIResin I Resin II Resin III 60--60-- -60--60- --60--60 세라믹 안료Ceramic pigment 2525 2525 2525 멜라민 수지Melamine resin 15.215.2 13.113.1 10.910.9 블록이소시아네이트수지Block Isocyanate Resin 22 22 22 첨가제*additive* 4.24.2 4.24.2 4.24.2 반응 촉매Reaction catalyst 0.150.15 0.150.15 0.150.15 합계Sum 114.88114.88 112.78112.78 110.58110.58

(*첨가제 ; 분산제, 침강방지제, 자외선 안정제가 포함된다)(* Additives include dispersant, sedimentation inhibitor, UV stabilizer)

표 2에 나타난 각 실시예에 따른 도료 조성물은 다음과 같은 방식으로 제조하였다. 1차적으로 용제 일부와 실리콘 변성 아크릴 수지 일부, 안료 전량, 분산제를 혼합하여 입도 7 마이크론 이상으로 분산시키고, 나머지 용제와 실리콘 변성 아크릴수지, 멜라민수지, 블록이소시아네이트 수지, 첨가제, 반응 촉매를 넣어 교반함으로써 1액형의 도료 조성물을 제조하였다.The coating composition according to each example shown in Table 2 was prepared in the following manner. Firstly, a part of the solvent, a part of the silicone-modified acrylic resin, a whole amount of pigment, and a dispersant are mixed and dispersed to a particle size of 7 microns or more. A one-part coating composition was prepared.

2액형 아크릴실리콘계 도료 조성물과의 물성 및 저장성에 대한 비교를 위하여 종래에 대한페인트잉크(주)에서 출원한 특허에서의 도료 조성물을 비교예로 하여 특성을 비교하였다.In order to compare the physical properties and shelf life with the two-component acrylic silicone coating composition, the characteristics of the coating compositions in the patent application filed by Paint Ink Co., Ltd. were compared.

물성 평가를 위하여 10 마이크론 두께로 하도 도장된 아연도강판에 본 발명의 도료 조성물과 비교예의 도료 조성물을 건조 도막 두께 25∼35 마이크론으로 도장하여 평가하였다. 건조조건은 180℃에서 15분으로 하였다.For evaluation of physical properties, the coating composition of the present invention and the coating composition of the comparative example were coated with a dry coating thickness of 25 to 35 microns on a galvanized steel sheet coated with a thickness of 10 microns. Drying conditions were 15 minutes at 180 degreeC.

아래의 표 3에는 각 도료 조성물을 사용하여 제조된 도막에 대한 물성 항목평가 결과를 나타내었다.Table 3 below shows the physical property evaluation results for the coating film prepared using each coating composition.

물성항목Property item 실험방법Experiment method 실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 비교예*Comparative Example * 촉진내후성(%)Promoted weather resistance (%) WOM2000hrsWOM2000hrs 9595 9696 9595 90 이상over 90 QUV2000hrsQUV2000hrs 9797 9797 9696 90 이상over 90 연필경도Pencil hardness 미쓰비시연필Mitsubishi pencil 4H-4H- 4H-4H- 4H4H 4H4H 내염수분무성Salt water spray resistance 5% NaCl,35℃ 500hrs5% NaCl, 35 ℃ 500hrs 양호Good 양호Good 양호Good 양호Good 내비등수성Boiling water resistance 끓는물에 6hrs 함침6hrs impregnation in boiling water 양호Good 양호Good 양호Good 양호Good 내충격성(cm)Impact resistance (cm) 300gr×10mm,1/2"300gr × 10mm, 1/2 " 2020 2020 2020 2020 부착성Adhesion 1mm crosscut, 100/1001mm crosscut, 100/100 100/100100/100 100/100100/100 100/100100/100 100/100100/100 내알칼리성Alkali resistance 5% NaOH,24hr spot5% NaOH, 24hr spot 양호Good 양호Good 양호Good 양호Good 내산성Acid resistance 5% H2SO4,24hr spot5% H 2 SO 4 , 24hr spot 양호Good 양호Good 양호Good 양호Good 내용제성Solvent resistance MEK rubbing 100회MEK rubbing Episode 100 100회100 times 100회100 times 100회100 times 100회100 times 내수성Water resistance 40℃, 500hrs40 ℃, 500hrs 양호Good 양호Good 양호Good 양호Good 재도장성Repaintable 1mm crosscut, 100/1001mm crosscut, 100/100 100/100100/100 100/100100/100 100/100100/100 100/100100/100 광택Polish (60°)(60 °) 9393 8989 8787 8888 저장성**Storability ** 60℃, 336hrs60 ℃, 336hrs 양호Good 양호Good 양호Good 겔화, 응고Gelling, coagulation

*비교예는 대한페인트잉크(주)에서 출원한 대한민국 특허 출원 번호 제95-16615에서 개시하는 2액형 아크릴실리콘계 도료 조성물을 사용한 경우에 대한 것이다.* A comparative example is for the case of using the two-component acrylic silicone coating composition disclosed in Korea Patent Application No. 95-16615 filed by Korea Paint Ink Co., Ltd.

**저장성은 초기점도 70Ku에서 저장 후에도 70±5Ku 이내의 점도변화를 보일때를 양호하다고 판단하였다.** Storability was judged to be good when the viscosity was changed within 70 ± 5Ku even after storage at the initial viscosity of 70Ku.

상기의 물성항목 평가에서 알 수 있듯이 본 발명의 도료조성물은 1액형이면서 종래의 2액형 아크릴실리콘계 도료 조성물의 특징인 고내후성, 고경도, 내스크레치성, 내약품성등의 물성과 동등 내지 그 이상의 도막 성질을 가지면서 저장성에 문제가 없는 우수한 것이다.As can be seen from the above evaluation of the physical properties, the coating composition of the present invention is a one-part type and a coating film equivalent to or higher than the properties of high weather resistance, high hardness, scratch resistance, chemical resistance, etc., which are characteristic of the conventional two-component acrylic silicone coating composition. It has excellent properties and no problem in storage.

이상과 같이 본 발명의 1액형 실리콘 변성 아크릴계 도료 조성물은 종래의 2액형 아크릴실리콘계 도료 조성물을 1액형화함으로써 도장작업시 주제와 경화제를 혼합해야하는 과정이 없고, 2액형이 갖고 있는 가사 시간에 따른 도장작업시간의 제약을 해소하도록 하였다.As described above, the one-component silicone-modified acrylic coating composition of the present invention does not have to mix the main agent and the curing agent during the painting work by one-component molding of the conventional two-component acrylic silicone coating composition, and the coating according to the pot life of the two-component coating. The work time restrictions were removed.

본 발명의 도료 조성물은 종래의 2액형 아크릴실리콘계 도료 조성물이 갖고 있는 고내후성, 고경도, 내스크레치성, 내약품성등의 우수한 도막물성을 동등내지 그 이상으로 나타낸다. 이에 더하여, 본 발명의 도료 조성물은 저장성에 문제가 없는 것이다.The coating composition of the present invention exhibits excellent coating properties such as high weather resistance, high hardness, scratch resistance, and chemical resistance of conventional two-component acrylic silicone coating compositions. In addition, the coating composition of the present invention has no problem in shelf life.

이상에서는 본 발명의 실시예에 따라 본 발명이 설명되었지만, 본 발명의 사상을 일탈하지 않는 범위 내에서 다양한 변형이 가능함은 본 발명이 속하는 기술 분야의 당업자라면 명확히 인지할 수 있을 것이다.Although the present invention has been described above according to an embodiment of the present invention, it will be apparent to those skilled in the art that various modifications may be made without departing from the spirit of the present invention.

Claims (10)

산가 5 내지 15, 알코올가 30 내지 100, 중량평균분자량 15,000 내지 30,000, 불휘발분 40내지 70%, 유리전이온도 30 내지 70℃이고, 실록산 결합을 갖는 실리콘 변성 아크릴수지 35 내지 65중량부;An acid value of 5 to 15, an alcohol of 30 to 100, a weight average molecular weight of 15,000 to 30,000, a nonvolatile content of 40 to 70%, a glass transition temperature of 30 to 70 ° C, and 35 to 65 parts by weight of a silicone-modified acrylic resin having a siloxane bond; 제1 경화제로서 메톡시메칠 및 메톡시메칠-이미노 관능기를 갖는 멜라민 수지를 8 내지 18중량부; 및8 to 18 parts by weight of a melamine resin having methoxymethyl and methoxymethyl-imino functional groups as the first curing agent; And 제2 경화제로서 헥사메칠렌디이소시아네이트타입의 수지인 블록이소시아네이트 수지를 0.6 내지 3.0중량부를 포함하는 1액형 실리콘 변성 아크릴계 도료 조성물.1-part silicone modified acrylic coating composition containing 0.6-3.0 weight part of block isocyanate resins which are hexamethylene diisocyanate type resin as a 2nd hardening | curing agent. 삭제delete 삭제delete 제1항에 있어서, 분산제, 침강 방지제 또는 자외선 안정제를 더 포함하는 것을 특징으로 하는 도료 조성물.The coating composition according to claim 1, further comprising a dispersant, an antisettling agent or an ultraviolet stabilizer. 40 내지 60 중량부의 아크릴 단량체, 15 내지 35 중량부의 용제 및 반응 개시제를 혼합하여 하이드록시기를 포함하며 알코올가가 70 내지 170 범위인 아크릴 수지를 제조하는 단계;Mixing 40 to 60 parts by weight of an acrylic monomer, 15 to 35 parts by weight of a solvent and a reaction initiator to prepare an acrylic resin containing a hydroxyl group and having an alcohol value in the range of 70 to 170; 얻어지는 아크릴 수지와 하이드록시기 또는 메톡시기를 갖고, 분자량이 500∼3,000 이며 규소 함량이 3∼20%인 실리콘 중간체 5 내지 20 중량부를 탈수 반응시켜 실록산 결합을 갖는 실리콘 변성 아크릴 수지를 제조하는 단계; 및Preparing a silicone-modified acrylic resin having a siloxane bond by dehydrating 5 to 20 parts by weight of a silicon intermediate having an acrylic resin, a hydroxyl group or a methoxy group, a molecular weight of 500 to 3,000 and a silicon content of 3 to 20%; And 상기 실리콘 변성 아크릴 수지에 제1 경화제인 멜라민 수지 및 제2 경화제인 블록이소시아네이트 수지를 첨가하는 단계를 포함하는 1액형 실리콘 변성 아크릴계 도료 조성물의 제조 방법.A method for producing a one-part silicone modified acrylic coating composition comprising adding a melamine resin as a first curing agent and a block isocyanate resin as a second curing agent to the silicone-modified acrylic resin. 제5항에 있어서, 상기 아크릴 단량체가 메틸메타크릴레이트, 메틸아크릴레이트, 에틸아크릴레이트, 스티렌, 2-에틸헥실아크릴레이트, 노말-부틸 아크릴레이트, 2-하이드록시에틸 메타크릴레이트, 2-하이드록시에틸 아크릴레이트, 메타크릴산 및 아크릴산으로 이루어진 군에서 선택된 적어도 하나인 것을 특징으로 하는 제조 방법.The method of claim 5, wherein the acrylic monomer is methyl methacrylate, methyl acrylate, ethyl acrylate, styrene, 2-ethylhexyl acrylate, normal- butyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxy At least one selected from the group consisting of oxyethyl acrylate, methacrylic acid and acrylic acid. 제5항에 있어서, 상기 용제가 크실렌, 셀루솔브아세테이트 및 코코졸-100으로 이루어진 군에서 선택된 적어도 하나이고, 상기 반응 개시제가 유기과산화물계 라디칼 개시제인 것을 특징으로 하는 제조 방법.The method according to claim 5, wherein the solvent is at least one selected from the group consisting of xylene, cellulsolve acetate and cocozol-100, and the reaction initiator is an organic peroxide radical initiator. 제5항에 있어서, 상기 실리콘 변성 아크릴 수지의 제조 단계에서 반응촉진제로서 유기 티탄계 화합물을 더 첨가하는 것을 특징으로 하는 제조 방법.The method according to claim 5, wherein an organic titanium compound is further added as a reaction accelerator in the step of producing the silicone-modified acrylic resin. 삭제delete 제5항에 있어서, 상기 경화제의 첨가시 방향족계 설폰산 또는 인산계 반응 촉매를 0.1∼3 중량부 더 첨가하는 것을 특징으로 하는 제조 방법.The method according to claim 5, wherein 0.1 to 3 parts by weight of an aromatic sulfonic acid or a phosphoric acid reaction catalyst is further added when the curing agent is added.
KR10-2000-0087440A 2000-12-30 2000-12-30 One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same KR100413852B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR10-2000-0087440A KR100413852B1 (en) 2000-12-30 2000-12-30 One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR10-2000-0087440A KR100413852B1 (en) 2000-12-30 2000-12-30 One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same

Publications (2)

Publication Number Publication Date
KR20020059059A KR20020059059A (en) 2002-07-12
KR100413852B1 true KR100413852B1 (en) 2004-01-07

Family

ID=27690288

Family Applications (1)

Application Number Title Priority Date Filing Date
KR10-2000-0087440A KR100413852B1 (en) 2000-12-30 2000-12-30 One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same

Country Status (1)

Country Link
KR (1) KR100413852B1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100986617B1 (en) 2008-12-31 2010-10-08 주식회사 노루홀딩스 Anti-corrosion coating composition and method of manufacturing the same
KR20200020321A (en) 2018-08-17 2020-02-26 김철기 Environmentally Modified Acrylic Coating Composition and Method for Recovering Poor Manholes Using the Same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100431882B1 (en) * 2001-12-31 2004-05-17 주식회사 디피아이 Glass Paint Composition
KR102269267B1 (en) * 2019-07-18 2021-06-25 국방과학연구소 High weatherability infrared low emissivity paint material compositions

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR960001064A (en) * 1994-06-03 1996-01-25 김충세 Paint composition
JPH10101995A (en) * 1996-09-30 1998-04-21 Toyota Motor Corp One-package low-temperature curing clear coating material
JPH10298495A (en) * 1997-04-22 1998-11-10 Nippon Paint Co Ltd Curable one-package silicone-modified acrylic emulsion coating composition
KR19990075667A (en) * 1998-03-13 1999-10-15 양성민 Low Pollution Coating Composition
JP2000129172A (en) * 1998-10-27 2000-05-09 Nagashima Tokushu Toryo Kk Heat-shielding coating and its coating method
KR20020003439A (en) * 2000-07-03 2002-01-12 김장연 Curable composition for modified silicone acryl resin and its preparing method

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR960001064A (en) * 1994-06-03 1996-01-25 김충세 Paint composition
KR0127783B1 (en) * 1994-06-03 1997-12-26 김충세 Composition for 1-component automobile paint
JPH10101995A (en) * 1996-09-30 1998-04-21 Toyota Motor Corp One-package low-temperature curing clear coating material
JPH10298495A (en) * 1997-04-22 1998-11-10 Nippon Paint Co Ltd Curable one-package silicone-modified acrylic emulsion coating composition
KR19990075667A (en) * 1998-03-13 1999-10-15 양성민 Low Pollution Coating Composition
JP2000129172A (en) * 1998-10-27 2000-05-09 Nagashima Tokushu Toryo Kk Heat-shielding coating and its coating method
KR20020003439A (en) * 2000-07-03 2002-01-12 김장연 Curable composition for modified silicone acryl resin and its preparing method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100986617B1 (en) 2008-12-31 2010-10-08 주식회사 노루홀딩스 Anti-corrosion coating composition and method of manufacturing the same
KR20200020321A (en) 2018-08-17 2020-02-26 김철기 Environmentally Modified Acrylic Coating Composition and Method for Recovering Poor Manholes Using the Same

Also Published As

Publication number Publication date
KR20020059059A (en) 2002-07-12

Similar Documents

Publication Publication Date Title
US5221581A (en) Coating composition of a glycidyl acrylic polymer, an aminoester acrylic polymer and a polyester or a polyesterurethane
ES2364119T3 (en) COMPOSITIONS FOR PAINTINGS, METHOD FOR APPLYING A FINISHING PAINT AND OBJECTS SO PAINTED.
US5290848A (en) Coating composition of a glycidyl acrylic polymer, an aminoester acrylic polymer and a polyester or a polyesterurethane
US5532027A (en) UV light treatment of clear coat to improve acid etch resistance
KR20010031106A (en) Coating compositions containing non-aqueous dispersed polymer, a silane functional acrylic polymer and a triazine
US4812506A (en) Amino methyl propanol blocked aromatic sulfonic acid
KR100507414B1 (en) Amino resins having carbamate groups as functional groups and coating compositions containing them
MXPA97009952A (en) Aminoresin functionalized with carbamate groups and coating compositions that contains them
KR100413852B1 (en) One-liquid Type Silicon-Modified and Acryl-based Paint Composition and Method of Preparing the Same
JP2005095723A (en) Coating method
JP4073180B2 (en) Resin composition for coating and curable coating composition
JP7042679B2 (en) Aqueous dressing
EP0494481A1 (en) Coating composition of acrylic polymers containing reactive groups and an epoxy organosilane
JPH10503534A (en) Curable resin composition, coating composition, coating film forming method and coated article
US4515835A (en) High solids thermosetting coating compositions, cured coatings, coated articles, and processes
EP0029597A1 (en) An aqueous thermosetting acrylic coating composition, articles coated therewith, and process for preparing said coated articles
EP3399002B1 (en) Highly scratch resistant one-pack type paint composition
KR101958544B1 (en) Paint composition
JP3249823B2 (en) Curable resin composition, coating composition, coating film forming method, and coated article
EP0935642B1 (en) Heat-hardenable paint compositions
JP4509128B2 (en) Resin composition for coating and curable coating composition
US6156862A (en) Heat-hardenable paint compositions
KR20000046452A (en) Paint composition for use in automobiles
JPH0782525A (en) Coating resin composition
JP2001072919A (en) Resin composition for coating and coating

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: 20121004

Year of fee payment: 10

FPAY Annual fee payment

Payment date: 20130902

Year of fee payment: 11

FPAY Annual fee payment

Payment date: 20140904

Year of fee payment: 12

FPAY Annual fee payment

Payment date: 20150910

Year of fee payment: 13

FPAY Annual fee payment

Payment date: 20160929

Year of fee payment: 14

LAPS Lapse due to unpaid annual fee