JP2006028470A - Antistaining paint, antistaining sheet, and method for producing the same - Google Patents
Antistaining paint, antistaining sheet, and method for producing the same Download PDFInfo
- Publication number
- JP2006028470A JP2006028470A JP2004273105A JP2004273105A JP2006028470A JP 2006028470 A JP2006028470 A JP 2006028470A JP 2004273105 A JP2004273105 A JP 2004273105A JP 2004273105 A JP2004273105 A JP 2004273105A JP 2006028470 A JP2006028470 A JP 2006028470A
- Authority
- JP
- Japan
- Prior art keywords
- antifouling
- silica sol
- sheet
- paint according
- colloidal silica
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
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- 239000003973 paint Substances 0.000 title claims abstract description 67
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
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- 229910052763 palladium Inorganic materials 0.000 description 1
- GCKZNUDNTDWGFM-UHFFFAOYSA-N pentane-2,4-dione;tin Chemical class [Sn].CC(=O)CC(C)=O GCKZNUDNTDWGFM-UHFFFAOYSA-N 0.000 description 1
- DAFIBNSJXIGBQB-UHFFFAOYSA-N perfluoroisobutene Chemical group FC(F)=C(C(F)(F)F)C(F)(F)F DAFIBNSJXIGBQB-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
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- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
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- 230000002940 repellent Effects 0.000 description 1
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- 238000007650 screen-printing Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
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- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
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- 229910052712 strontium Inorganic materials 0.000 description 1
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
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Images
Landscapes
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
Abstract
Description
本発明は、汚染防止塗料、汚染防止シートおよびその製造方法に関する。 The present invention relates to an antifouling paint, an antifouling sheet and a method for producing the same.
近年、種々の機能性材料が開発され、広範な分野に応用され、その機能の中には汚染防止機能が挙げられる。従来から汚染防止処理法として、汚染防止塗料を用いて建築物、建材素材、車輌、土木関係などの物品の表面に汚染防止塗膜を形成する方法が実施されてきた。特に、フッ素系樹脂、シリコーン系樹脂、アクリル系樹脂、ウレタン系樹脂、それら共重合体などが、耐久性に優れていることから汚染防止塗料の塗膜形成成分として使用されている。しかしながら、これらの塗料から形成される汚染防止塗膜は、長期にわたり屋外に曝されると、自然環境下において紫外線による劣化により、グロスの低下、塗膜亀裂の発生、雨などによる耐水性劣化(加水分解劣化)、油成分などの付着と雨水によってすじ状に汚染されるなど、塗膜表面が変化するという問題がある。これらの問題を解決する汚染防止処理方法には、非特許文献1の「フラクタル構造による超撥水/撥油表面」においては、塗膜表面に微細な凸凹構造を形成することにより濡れの因子を支配し、これにより塗膜に撥水撥油性を付与することが紹介されている。しかし、塗料を物品に塗布して上記の如き機能を発現させることは、現行塗工技術では非常に困難である。 In recent years, various functional materials have been developed and applied to a wide range of fields. Conventionally, as a pollution prevention treatment method, a method of forming a pollution prevention coating film on the surface of an article such as a building, a building material material, a vehicle, or civil engineering using a pollution prevention coating has been carried out. In particular, fluorine resins, silicone resins, acrylic resins, urethane resins, copolymers thereof, and the like are used as coating film forming components of antifouling paints because of their excellent durability. However, antifouling coatings formed from these paints, when exposed to the outdoors for a long time, deteriorated due to ultraviolet rays in the natural environment, resulting in a decrease in gloss, occurrence of cracks in the coating, and water resistance deterioration due to rain ( There is a problem that the surface of the coating film changes, such as hydrolysis degradation), adhesion of oil components and the like, and contamination by rainwater. In the antifouling treatment method for solving these problems, in “Super water / oil repellent surface by fractal structure” of Non-Patent Document 1, a wetting factor is formed by forming a fine uneven structure on the coating film surface. It has been introduced that it imparts water and oil repellency to the coating. However, it is very difficult to apply the coating material to the article to develop the above-described functions with the current coating technique.
また、有機溶剤可溶型で反応性基を含有するフッ素樹脂を含む塗料が多くの建築物、建材、車輌、機械向け汚染防止塗料として使用されている(特許文献1および2)。しかしながら、前記の如く、これらの汚染防止塗料からなる塗膜は、紫外線による耐久性の問題と、油成分付着および雨水によるすじ状汚染が発生するといった問題がある。また、フッ素系樹脂は、非特許文献2において、ポリマーヒューム熱の発生や熱分解により毒性の高いフッ化カルボニル、パーフロロイソブチレン、フッ化水素などを発生し、人体に対する毒性が高いと考える。また、同様にフッ素系化合物であるテロマーも同様であり、加えて人体に対する安全性が確認されていない。 Also, organic solvent-soluble paints containing fluororesins containing reactive groups are used as anti-fouling paints for many buildings, building materials, vehicles, and machines (Patent Documents 1 and 2). However, as described above, the coating film made of these anti-contamination paints has the problem of durability due to ultraviolet rays and the problem that oil component adhesion and streak-like contamination due to rainwater occur. Further, in Non-Patent Document 2, it is considered that the fluororesin generates highly toxic carbonyl fluoride, perfluoroisobutylene, hydrogen fluoride, and the like due to the generation of polymer fume heat and thermal decomposition, and is highly toxic to the human body. Similarly, telomers that are fluorine compounds are the same, and in addition, safety to the human body has not been confirmed.
従って本発明の目的は、上記従来技術の問題点を解消し、長期的に汚染防止性能を示す汚染防止塗料、汚染防止シートおよびその製造方法を提供することである。 Accordingly, an object of the present invention is to solve the above-mentioned problems of the prior art and provide a pollution prevention paint, a pollution prevention sheet, and a method for producing the same, which exhibit long-term pollution prevention performance.
上記目的は以下の本発明によって達成される。すなわち、本発明は、塩基性触媒を用いて形成されたコロイダルシリカゾル(A)と親水性ポリマー(B)とを必須成分として含有していることを特徴とする汚染防止塗料を提供する。 The above object is achieved by the present invention described below. That is, the present invention provides a pollution control paint comprising colloidal silica sol (A) formed using a basic catalyst and a hydrophilic polymer (B) as essential components.
上記本発明の汚染防止塗料においては、コロイダルシリカゾル(A)のシリカが、表面にシラノール基(−Si−OH)を有する平均粒子径1nm〜200nmの超微粒子形状および/または表面にシラノール基(−Si−OH)を有する長鎖状のシリカであること;コロイダルシリカゾル(A)が、メチルまたはエチルシリケートモノマーおよび/またはメチルまたはエチルシリケートオリゴマーを原料とするシリカゾルであること;コロイダルシリカゾル(A)が、ケイ酸ナトリウムを原料とするシリカゾルであること;コロイダルシリカゾル(A)中のシリカと親水性ポリマー(B)との使用割合(質量比)が、シリカ:親水性ポリマー=5:95〜99:1であることが好ましい。 In the antifouling paint of the present invention, the silica of the colloidal silica sol (A) has an ultrafine particle shape with an average particle diameter of 1 nm to 200 nm having a silanol group (-Si-OH) on the surface and / or a silanol group (- The long-chain silica having Si—OH); the colloidal silica sol (A) is a silica sol using a methyl or ethyl silicate monomer and / or a methyl or ethyl silicate oligomer as a raw material; the colloidal silica sol (A) The silica sol using sodium silicate as a raw material; the use ratio (mass ratio) of silica and the hydrophilic polymer (B) in the colloidal silica sol (A) is silica: hydrophilic polymer = 5: 95 to 99: 1 is preferable.
また、上記本発明の汚染防止塗料においては、親水性ポリマー(B)が、ポリビニルアルコール、変性ポリビニルアルコール、ポリビニルピロリドン、変性ポリビニルピロリドン、親水性アクリル系ポリマー、親水性ウレタン系ポリマー、セルロース化合物、水溶性ナイロン、ポリビニルホルマール、ポリビニルアセタールおよびポリビニルベンザールから選ばれる少なくとも1種であること;さらにアルミナゾル、界面活性剤、紫外線吸収剤および架橋剤からなる群から選ばれる少なくとも1種を含むこと;該架橋剤が、カルボジイミド化合物、有機金属錯体化合物、ポリイソシアネート化合物、オキサゾリン化合物およびエポキシ化合物からなる群から選ばれる少なくとも1種であることが好ましい。 In the antifouling paint of the present invention, the hydrophilic polymer (B) is polyvinyl alcohol, modified polyvinyl alcohol, polyvinyl pyrrolidone, modified polyvinyl pyrrolidone, hydrophilic acrylic polymer, hydrophilic urethane polymer, cellulose compound, water-soluble compound. At least one selected from reactive nylon, polyvinyl formal, polyvinyl acetal and polyvinyl benzal; and further including at least one selected from the group consisting of alumina sol, surfactant, ultraviolet absorber and crosslinking agent; The agent is preferably at least one selected from the group consisting of carbodiimide compounds, organometallic complex compounds, polyisocyanate compounds, oxazoline compounds and epoxy compounds.
また、本発明は、基材シートと、該基材シートの一方の面に設けた汚染防止層とからなる汚染防止シートにおいて、該汚染防止層が、前記本発明の汚染防止塗料から形成されていることを特徴とする汚染防止シートを提供する。上記本発明の汚染防止シートにおいては、該汚染防止層の水に対する接触角が、20度以下であること;および汚染防止層の膜厚が0.01μm〜10μmであることが好ましい。
また、本発明は、基材シートの一方の面に前記本発明の汚染防止塗料を塗布し、常温〜120℃の温度で汚染防止層を形成することを特徴とする汚染防止シートの製造方法を提供する。
Further, the present invention provides a pollution control sheet comprising a base sheet and a pollution control layer provided on one surface of the base sheet, wherein the pollution control layer is formed from the pollution control paint of the present invention. A pollution control sheet is provided. In the pollution prevention sheet of the present invention, the contact angle of the pollution prevention layer with respect to water is preferably 20 degrees or less; and the thickness of the pollution prevention layer is preferably 0.01 μm to 10 μm.
In addition, the present invention provides a method for producing a pollution control sheet, characterized in that the pollution control paint of the present invention is applied to one surface of a substrate sheet, and a pollution prevention layer is formed at a temperature of room temperature to 120 ° C. provide.
本発明の汚染防止塗料からなる塗膜は、その最表面がシラノール基の−OH基により親水性となり、雨などの水蒸気によって水膜が形成され、汚染物が流れ落ちる機構である。発明者らは、雑誌(光触媒による環境浄化 触媒、36、524〜530(1994))において紹介されている手法として、光触媒効果と表面を親水性にすることで汚染防止効果が得られる現象をさらに発展させることで本発明に到達した。
なお、本発明において上記「シート」の用語は、「シート」および「フィルム」の双方を含む意味で使用している。
The coating film made of the antifouling paint of the present invention has a mechanism in which the outermost surface becomes hydrophilic by silanol-OH groups, a water film is formed by water vapor such as rain, and the contaminants flow down. As a technique introduced in the magazine (Environmental purification catalyst by photocatalyst, 36, 524 to 530 (1994)), the inventors further developed a phenomenon in which a photocatalytic effect and a pollution prevention effect can be obtained by making the surface hydrophilic. The present invention has been reached through development.
In the present invention, the term “sheet” is used to include both “sheet” and “film”.
本発明によれば、長期的に汚染防止性能を示す汚染防止塗料、汚染防止シートおよびその製造方法を提供することができる。 ADVANTAGE OF THE INVENTION According to this invention, the antifouling paint which shows antifouling performance for a long term, a fouling prevention sheet, and its manufacturing method can be provided.
次に発明を実施するための最良の形態を挙げて、本発明をさらに詳細に説明する。
本発明の汚染防止塗料は、塩基性触媒を用いて形成されたコロイダルシリカゾル(A)と親水性ポリマー(B)の2成分を必須とする無機−有機複合物を含有することを特徴としている。本発明で使用するコロイダルシリカゾルとは、塩基性触媒を用いて形成されたコロイド状のシリカの水分散体であって、該コロイダルシリカは式SiOn(OH)m(OR)oで表わされる化合物であって、粒子表面に多数のシラノール基を有している。該シラノール基の存在によってゾルの安定性に優れ、該コロイダルシリカを含む汚染防止層は親水性であり、基材との密着性に優れ、さらに適当な架橋剤によって架橋すること(自己架橋、有機無機の架橋)により、汚染防止層の硬度アップを図ることができる。これに対して酸性触媒を用いて形成されたコロイド状のシリカゾルは、安定性に劣り、本発明の目的には不適当である。
Next, the present invention will be described in more detail with reference to the best mode for carrying out the invention.
The antifouling paint of the present invention is characterized in that it contains an inorganic-organic composite comprising two components of a colloidal silica sol (A) and a hydrophilic polymer (B) formed using a basic catalyst. The colloidal silica sol used in the present invention is an aqueous dispersion of colloidal silica formed using a basic catalyst, and the colloidal silica is a compound represented by the formula SiO n (OH) m (OR) o . And it has many silanol groups on the particle | grain surface. Due to the presence of the silanol group, the sol is excellent in stability, and the anti-contamination layer containing the colloidal silica is hydrophilic, has excellent adhesion to the base material, and is crosslinked with an appropriate crosslinking agent (self-crosslinking, organic By the inorganic crosslinking, it is possible to increase the hardness of the contamination prevention layer. On the other hand, colloidal silica sol formed using an acidic catalyst is inferior in stability and is not suitable for the purpose of the present invention.
塩基性触媒を用いて形成された一般的なシリカゾルとは、図1に示すように粒子の外側にシラノール基が存在しているが、組成式としてはSiOn(OH)m(OR)o(n=1.95〜2.0、m=0〜0.1、o=0〜0.5、n+0.5m=2.0となる比、RはCH3またはC2H5である)で表わされる。本発明に使用するコロイダルシリカゾルとしては、ポリアルコキシシロキサン誘導体から合成されるような図2で示される長鎖状のコロイダルシリカゾルも使用できる。このシリカゾルは、組成式がSiOn(OH)m(OR)o(n=1.5〜1.95、m=0.1〜1.0、o=0〜0.5、n+0.5m+0.5o=2.0となる比、RはCH3またはC2H5である)で示される、シラノール基(−Si−OH)の数が多いものである。 As shown in FIG. 1, a general silica sol formed using a basic catalyst has silanol groups on the outside of the particle, but the composition formula is SiO n (OH) m (OR) o ( n = 1.95-2.0, m = 0-0.1, o = 0-0.5, ratio of n + 0.5m = 2.0, R is CH 3 or C 2 H 5 ) Represented. As the colloidal silica sol used in the present invention, the long-chain colloidal silica sol shown in FIG. 2 synthesized from a polyalkoxysiloxane derivative can also be used. This silica sol has a composition formula of SiO n (OH) m (OR) o (n = 1.5 to 1.95, m = 0.1 to 1.0, o = 0 to 0.5, n + 0.5 m + 0. 5 o = 2.0 ratio, R is CH 3 or C 2 H 5 ), and the number of silanol groups (—Si—OH) is large.
以上のようなコロイダルシリカゾルは種々のものが市販されているが、コロイダルシルカゾルは、表面のシラノール基(−Si−OH)を有する平均粒子径1nm〜200nmの超微粒子形状および/または表面にシラノール基(−Si−OH)を有する長鎖状のシリカからなるゾルであることが好ましい。また、コロイダルシリカゾルが、メチルシリケートモノマー、エチルシリケートモノマー、メチルシリケートオリゴマーまたはエチルシリケートオリゴマーを原料とし、塩基性触媒を用いて形成されたシリカゾル、ケイ酸ナトリウムを原料とし、塩基性触媒を用いて形成されたシリカゾルであることが好ましい。以上の如きコロイダルシルカゾルとしては、例えば、商品名としてスノーテックス(日産化学(株)製)、カタロイドS(触媒化成工業(株)製)、ルドックス(グレース社製)、シリカドール(日本化学工業(株)製)、クォートロン(扶桑化学(株)製)、アデライト(旭電化工業(株)製)、MKCシリケートMSH(三菱化学(株)製)などが市場から入手して本発明で使用できる。 Various colloidal silica sols as described above are commercially available. Colloidal silica sols are ultrafine particles having an average particle diameter of 1 nm to 200 nm having silanol groups (—Si—OH) on the surface and / or silanols on the surface. A sol made of long-chain silica having a group (—Si—OH) is preferable. In addition, colloidal silica sol is formed using methyl silicate monomer, ethyl silicate monomer, methyl silicate oligomer or ethyl silicate oligomer as raw materials, silica sol formed using basic catalyst, sodium silicate as raw material, and using basic catalyst It is preferable to be a silica sol. Examples of the colloidal silica sol as described above include, as trade names, Snowtex (manufactured by Nissan Chemical Co., Ltd.), Cataloid S (manufactured by Catalytic Chemical Industry Co., Ltd.), Ludox (manufactured by Grace Co., Ltd.), silica doll (Nippon Chemical Industry Co., Ltd.). Quartron (manufactured by Fuso Chemical Co., Ltd.), Adelite (manufactured by Asahi Denka Kogyo Co., Ltd.), MKC silicate MSH (manufactured by Mitsubishi Chemical Co., Ltd.) and the like can be obtained from the market and used in the present invention. .
本発明で使用する親水性ポリマーとは、ポリビニルアルコール、変性ポリビニルアルコール(アクリルアミド、不飽和カルボン酸、スルホン酸モノマー、カチオン性モノマー、不飽和シランモノマー、不飽和エチレンオキサイドモノマーなどとの共重合物)、ポリビニルピロリドン、変性ポリビニルピロリドン(酢酸ビニル、不飽和イミダゾール、ビニルカプロラクトンなどとの共重合物)、ポリアクリル酸、ポリアクリル酸塩類、ポリアクリルアミド、ポリイソプロピルアクリルアミド、ポリホルムアミド、ポリエチレングリコール、デンプン、変性デンプン、ゼラチン、カゼイン、アルギン、セルロース化合物(カルボキシメチルセルロース、メチルセルロース、エチルセルロース、ヒドロキシエチルセルロースなど)、水溶性ナイロン、ポリビニルホルマール、ポリビニルアセタール、ポリビニルベンザール、ポリウレタン、キチン類、キトサン類などが挙げられる。以上列記した親水性ポリマーは本発明において使用する好ましい化合物であって本発明はこれらの例示の化合物に限定されるものではない。従って上述の例示の化合物のみならず、その他現在市販されており、市場から容易に入手し得る化合物はいずれも本発明において使用することができる。 The hydrophilic polymer used in the present invention is polyvinyl alcohol, modified polyvinyl alcohol (a copolymer of acrylamide, unsaturated carboxylic acid, sulfonic acid monomer, cationic monomer, unsaturated silane monomer, unsaturated ethylene oxide monomer, etc.) , Polyvinyl pyrrolidone, modified polyvinyl pyrrolidone (copolymerized with vinyl acetate, unsaturated imidazole, vinyl caprolactone, etc.), polyacrylic acid, polyacrylates, polyacrylamide, polyisopropylacrylamide, polyformamide, polyethylene glycol, starch, modified Starch, gelatin, casein, algin, cellulose compounds (carboxymethylcellulose, methylcellulose, ethylcellulose, hydroxyethylcellulose, etc.), water-soluble nylon Polyvinyl formal, polyvinyl acetal, polyvinyl benzal, polyurethanes, chitins, and chitosans and the like. The hydrophilic polymers listed above are preferred compounds used in the present invention, and the present invention is not limited to these exemplified compounds. Accordingly, not only the above-exemplified compounds but also any other compounds that are currently commercially available and can be easily obtained from the market can be used in the present invention.
本発明の汚染防止塗料は、水性媒体中に前記のコロイダルシリカゾルと上記の親水性ポリマーとを含むことを必須としており、コロイダルシリカゾル(A)中のシリカと親水性ポリマー(B)との使用割合(質量比)はシリカ:親水性ポリマー=5:95〜99:1の範囲が好ましく、さらに好ましくはシリカ:親水性ポリマー=20:80〜95:5の範囲である。上記において親水性ポリマーの使用量が多過ぎると、形成される汚染防止層の水に対する接触角が大きくなり汚染防止性が発揮されるまでの時間が長くなるなどの点で問題があり、一方、親水性ポリマーの使用量が少な過ぎると、汚染防止塗料を基材に塗布し乾燥するときに、クラックにより汚染防止層に凹凸が生じて外観不良や透明性などの点で問題がある。また、本発明の汚染防止塗料の固形分濃度は、約5〜15質量%の範囲が好ましく、固形分濃度が低過ぎると汚染防止層の形成時に塗工ムラや乾燥時間がかかるなどの点で問題があり、一方、固形分濃度が高過ぎると汚染防止塗料の液安定性が低下する。 The antifouling paint of the present invention requires that the aqueous colloidal silica sol and the hydrophilic polymer are contained in an aqueous medium, and the use ratio of silica and the hydrophilic polymer (B) in the colloidal silica sol (A). (Mass ratio) is preferably in the range of silica: hydrophilic polymer = 5: 95 to 99: 1, and more preferably in the range of silica: hydrophilic polymer = 20: 80 to 95: 5. If the amount of the hydrophilic polymer used is too large in the above, there is a problem in that the contact angle with respect to the water of the contamination prevention layer to be formed is increased and the time until the contamination prevention property is exerted becomes longer, When the amount of the hydrophilic polymer used is too small, when the antifouling paint is applied to the substrate and dried, the antifouling layer is uneven due to cracks, which causes problems such as poor appearance and transparency. In addition, the solid content concentration of the antifouling paint of the present invention is preferably in the range of about 5 to 15% by mass, and if the solid content concentration is too low, coating unevenness and drying time are required when forming the antifouling layer. On the other hand, if the solid content concentration is too high, the liquid stability of the antifouling paint is lowered.
本発明の汚染防止塗料の液媒体は、水を主体とし、水としてはイオン交換水を使用することが好ましい。また、水と有機溶剤との混合物も液媒体として使用することができる。好ましい有機溶剤として、例えば、ケトン系溶媒(アセトン、メチルエチルケトン、メチルイソブチルケトン、シクロヘキサノンなど)、アルコール系溶剤(メタノール、エタノール、イソプロパノールなど)、エーテル系溶剤(ジオキサン、テトラヒドロフランなど)、エステル系溶剤(酢酸エチル、酢酸ブチル、酢酸イソブチルなど)、グリコールエーテルエステル系溶剤(エチレングリコールエチルエーテルアセテート、プロピレングリコールメチルエーテルアセテート、3−メチル−3−メトキシブチルアセテート、エチル−3−エトキシプロピオネートなど)、アミド系溶剤(ジメチルホルムアミド、ジメチルアセトアミドなど)、ラクタム系溶剤(n−メチル−2−ピロリドンなど)が挙げられる。これらのうち、メタノール、エタノール、イソプロパノールなどのアルコールを用いることが好ましい。 The liquid medium of the antifouling paint of the present invention is mainly water, and it is preferable to use ion exchange water as the water. A mixture of water and an organic solvent can also be used as a liquid medium. Preferred organic solvents include, for example, ketone solvents (acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, etc.), alcohol solvents (methanol, ethanol, isopropanol, etc.), ether solvents (dioxane, tetrahydrofuran, etc.), ester solvents (acetic acid, etc.) Ethyl, butyl acetate, isobutyl acetate, etc.), glycol ether ester solvents (ethylene glycol ethyl ether acetate, propylene glycol methyl ether acetate, 3-methyl-3-methoxybutyl acetate, ethyl-3-ethoxypropionate, etc.), amides And solvent based solvents (such as dimethylformamide and dimethylacetamide) and lactam solvents (such as n-methyl-2-pyrrolidone). Of these, alcohols such as methanol, ethanol and isopropanol are preferably used.
本発明の汚染防止塗料はさらに架橋剤を含むことができる。該架橋剤は、最初から汚染防止塗料中に添加しておいてもよいし、汚染防止塗料の塗布時に汚染防止塗料に添加してもよい。架橋剤としては、親水性ポリマーが有している親水性基、例えば、カルボキシル基や水酸基を利用する架橋剤が使用できる。該架橋剤としては、例えば、エポキシ系架橋剤、カルボジイミド系架橋剤、オキサゾリン系架橋剤、水分散型イソシアネートまたは金属錯体系架橋剤などの従来から使用されている公知のものが使用でき、特に限定されない。例えば、エポキシ系架橋剤としては、「エピコート」(油化シェルエポキシ社製)などの従来公知の市販されているエポキシ樹脂を添加して使用することができる。カルボジイミド系架橋剤としては、「カルボジライト」の商品名(日清紡社製)の市販品を入手して使用することができる。オキサゾリン系架橋剤としては、「エポクロス」の商品名(日本触媒社製)の市販品を入手して使用することができる。 The antifouling paint of the present invention can further contain a crosslinking agent. The crosslinking agent may be added to the antifouling paint from the beginning, or may be added to the antifouling paint when the antifouling paint is applied. As the cross-linking agent, a cross-linking agent utilizing a hydrophilic group possessed by the hydrophilic polymer, for example, a carboxyl group or a hydroxyl group can be used. As the crosslinking agent, for example, conventionally known ones such as epoxy crosslinking agents, carbodiimide crosslinking agents, oxazoline crosslinking agents, water-dispersed isocyanates or metal complex crosslinking agents can be used, and particularly limited. Not. For example, as an epoxy-based crosslinking agent, conventionally known commercially available epoxy resins such as “Epicoat” (manufactured by Yuka Shell Epoxy Co., Ltd.) can be added and used. As the carbodiimide-based cross-linking agent, a commercially available product under the trade name “Carbodilite” (manufactured by Nisshinbo) can be used. As the oxazoline-based cross-linking agent, a commercial product of “Epocross” (Nippon Shokubai Co., Ltd.) can be obtained and used.
水分散型イソシアネート系架橋剤としては、「デュラネート」の商品名(旭化成ケミカルズ社製)の市販品を入手して使用することができる。または、金属錯体系架橋剤としては、チタン有機化合物系、「オルガチックス」の商品名(松本製薬工業社製)で市販されているジルコニウム有機化合物系が入手可能であり、アルミニウム、クロム、コバルト、銅、鉄、ニッケル、バナジウム、亜鉛、インジウム、カルシウム、マグネシウム、マンガン、イットリウム、セリウム、ストロンチウム、パラジウム、バリウム、モリブデニウム、ランタン、「ナーセム」の商品名(日本化学産業社製)で市販されているスズのアセチルアセトン錯体が入手して使用できる。これらの架橋剤は、適量であれば形成される汚染防止層の耐水性の向上に特に有効であるが、使用量が多過ぎると汚染防止層の汚染防止性能の低下を引き起こすため、汚染防止塗料の固形分100質量部に対して10質量部以下、好ましくは0.01〜1.0質量部の範囲内の使用が好ましい。 As the water-dispersed isocyanate-based crosslinking agent, a commercial product of “Duranate” (trade name, manufactured by Asahi Kasei Chemicals) can be obtained and used. Alternatively, as the metal complex-based crosslinking agent, titanium organic compound-based, zirconium organic compound-based commercially available under the trade name “Orgatics” (manufactured by Matsumoto Pharmaceutical Co., Ltd.) are available, and aluminum, chromium, cobalt, Copper, iron, nickel, vanadium, zinc, indium, calcium, magnesium, manganese, yttrium, cerium, strontium, palladium, barium, molybdenium, lanthanum, marketed under the trade name “Narsem” (manufactured by Nippon Kagaku Sangyo Co., Ltd.) Tin acetylacetone complexes are available and can be used. These crosslinking agents are particularly effective for improving the water resistance of the antifouling layer to be formed in an appropriate amount. However, if the amount of use is excessive, the antifouling property of the antifouling layer is lowered. The solid content is 10 parts by mass or less, preferably 0.01 to 1.0 part by mass based on 100 parts by mass of the solid content.
また、本発明の汚染防止塗料には、必要に応じて従来公知の界面活性剤を少量加えてもよい。これらの界面活性剤としては、例えば、グリセリンモノオレート、グリセリンラウレート、グリセリンカプレート、ジグリセリンオレート、ジグリセリンラウレート、トリグリセリンオレートなどのグリセリン脂肪酸エステル類、ポリオキシエチレンアルキルエーテルなどのポリオキシエチレン脂肪アルコールエーテル類、ポリエチレングリコールオレート、ポリエチレングリコールラウレートなどのポリエチレングリコール脂肪酸エステル類、ポリオキシエチレンソルビタントリオレートなどのポリオキシエチレンソルビタン脂肪酸エステル類などが挙げられる。これらの界面活性剤の使用量は、特に限定されないが、使用する場合には、通常、汚染防止塗料の固形分100質量部に対して0.01〜5質量部、好ましくは0.1〜1質量部の範囲である。 Moreover, you may add a small amount of conventionally well-known surfactant to the pollution control paint of this invention as needed. Examples of these surfactants include glycerin monooleate, glycerin laurate, glycerin caprate, diglycerin oleate, diglycerin laurate, and triglycerin oleate, and polyoxyethylene alkyl ethers and other polyoxyethylene alkyl ethers. Examples include ethylene fatty alcohol ethers, polyethylene glycol fatty acid esters such as polyethylene glycol oleate and polyethylene glycol laurate, and polyoxyethylene sorbitan fatty acid esters such as polyoxyethylene sorbitan trioleate. Although the usage-amount of these surfactant is not specifically limited, When using, 0.01-5 mass parts normally with respect to 100 mass parts of solid content of a pollution control coating material, Preferably it is 0.1-1. It is the range of mass parts.
また、本発明の汚染防止塗料には、前記の親水性ポリマー以外に他の樹脂バインダーを添加してもよい。これらの樹脂バインダーとしては特に限定されないが、例えば、従来公知のシリコーン系樹脂、ポリエステル系樹脂、ポリアミド系樹脂、ポリイミド系樹脂、ポリスチレン系樹脂、ポリウレタン系樹脂、ポリカーボネート系樹脂、ノルボルネン系樹脂、セルロース系樹脂、ポリビニルブチラール系樹脂、ポリ酢酸ビニル系樹脂などが挙げられる。これらの樹脂の使用量は特に限定されないが、使用する場合には、通常、汚染防止塗料の固形分100質量部に対して800質量部以下、好ましくは5〜500質量部の範囲である。 In addition to the hydrophilic polymer, other resin binders may be added to the antifouling paint of the present invention. These resin binders are not particularly limited. For example, conventionally known silicone resins, polyester resins, polyamide resins, polyimide resins, polystyrene resins, polyurethane resins, polycarbonate resins, norbornene resins, and cellulose resins. Examples thereof include a resin, a polyvinyl butyral resin, and a polyvinyl acetate resin. Although the usage-amount of these resin is not specifically limited, When using, it is usually 800 mass parts or less with respect to 100 mass parts of solid content of a pollution control coating material, Preferably it is the range of 5-500 mass parts.
本発明の汚染防止塗料には、必要に応じてさらに添加剤を加えてもよい。例えば、酸化防止剤(ヒンダードフェノール系、ホスファイト系、チオエーテル系など)、光安定剤(ヒンダードアミン系など)、紫外線吸収剤(ベンゾフェノン系、ベンゾトリアゾール系など)、ガス変色安定剤(ヒドラジン系など)、金属不活性剤などやこれら2種類以上の併用が挙げられる。 If necessary, an additive may be added to the antifouling coating material of the present invention. For example, antioxidants (hindered phenols, phosphites, thioethers, etc.), light stabilizers (hindered amines, etc.), UV absorbers (benzophenones, benzotriazoles, etc.), gas discoloration stabilizers (hydrazines, etc.) ), A metal deactivator, or a combination of two or more of these.
さらに本発明の汚染防止塗料には、必要に応じてコロイダルシリカ以外の無機微粒子や有機微粒子を適宜使用することができる。無機微粒子としては、例えば、アルミナゾルが使用できる。上記の如きアルミナゾルとしては、例えば、アルミナゾル−100、アルミナゾル−200、アルミナゾル−520(日産化学工業(株)製)、カタロイドAS(触媒化学工業(株)製)、アルミナクリアゾル(川研ファインケミカル製)などを市場から入手して本発明で使用することができる。有機微粒子としては、例えば、シリコーン樹脂微粒子、フッ素樹脂微粒子、アクリル樹脂微粒子、ウレタン樹脂微粒子、ポリエチレン樹脂微粒子、反応性シロキサンなどを挙げることができる。 Furthermore, inorganic fine particles and organic fine particles other than colloidal silica can be appropriately used in the antifouling paint of the present invention as required. As the inorganic fine particles, for example, alumina sol can be used. Examples of the alumina sol as described above include alumina sol-100, alumina sol-200, alumina sol-520 (manufactured by Nissan Chemical Industries, Ltd.), cataloid AS (manufactured by Catalytic Chemical Industries, Ltd.), and alumina clear sol (manufactured by Kawaken Fine Chemicals). Etc.) can be obtained from the market and used in the present invention. Examples of the organic fine particles include silicone resin fine particles, fluororesin fine particles, acrylic resin fine particles, urethane resin fine particles, polyethylene resin fine particles, and reactive siloxane.
本発明の汚染防止塗料により汚染防止処理される対象としては、無機ガラス、ポリエチレンテレフタレートやポリエチレンナフタレートなどのポリエステル樹脂、ポリエチレンやポリプロピレンなどのポリオレフィン樹脂、ポリカーボネート樹脂、ポリメチルメタクリレート樹脂、ポリ塩化ビニル樹脂、セルロースエステル樹脂、ポリイミド樹脂、ポリアミド樹脂、ポリスルホンなどの透明樹脂のフィルム、射出成形品、キャスト成形品などが挙げられる。本発明は、農業用フィルムで用いられるエチレンからα−ポリオレフィン共重合体を主体とする樹脂、特に線状低密度ポリエチレン(LLDPE)から形成されている単層から多層のポリオレフィン系樹脂フィルムやポリエチレンテレフタレートなどのポリエステルフィルムに汚染防止性を付与するのに有用である。 Examples of the object to be subjected to antifouling treatment by the antifouling paint of the present invention include inorganic glass, polyester resins such as polyethylene terephthalate and polyethylene naphthalate, polyolefin resins such as polyethylene and polypropylene, polycarbonate resins, polymethyl methacrylate resins, and polyvinyl chloride resins. , Cellulose ester resins, polyimide resins, polyamide resins, transparent resin films such as polysulfone, injection molded products, cast molded products, and the like. The present invention relates to a resin mainly composed of an α-polyolefin copolymer from ethylene used in an agricultural film, particularly a single-layer to multi-layer polyolefin resin film or polyethylene terephthalate formed from linear low density polyethylene (LLDPE). It is useful for imparting antifouling properties to polyester films such as.
また、これらのプラスチックフィルムに汚染防止層を設ける場合、設けられた塗膜のプラスチックフィルムに対する接着強度と耐久性を付与するために汚染防止塗料の塗布に先立ってプラスチックフィルムにコロナ放電処理、プラズマ処理、下塗り処理、熱処理、除塵埃処理、アルカリ処理などの表面処理を施すことが好ましい。プラスチックフィルムに対するこれらの表面処理には、当該工業分野において周知の表面処理技術を利用し、本発明を実施することができる。上記成形品に汚染防止塗料の汚染防止層を形成するには、任意の塗装方法が採用される。例えば、スプレー法、ディップ法、フローコート法、ロールコート法、バーコート法、カーテンフロー法、スピンコート法、スクリーン印刷法、刷毛塗りなどの何れの方法でも差し支えない。 In addition, when a contamination prevention layer is provided on these plastic films, the corona discharge treatment and plasma treatment are applied to the plastic films prior to the application of the pollution prevention paint in order to impart adhesion strength and durability of the coating film to the plastic film. It is preferable to perform surface treatment such as undercoating treatment, heat treatment, dust removal treatment or alkali treatment. For these surface treatments for plastic films, the present invention can be carried out using surface treatment techniques well known in the industrial field. In order to form a pollution prevention layer of the pollution prevention paint on the molded article, any coating method is adopted. For example, any method such as spray method, dipping method, flow coating method, roll coating method, bar coating method, curtain flow method, spin coating method, screen printing method, and brush coating may be used.
本発明に係る汚染防止塗料は物品の表面に塗布し、強制乾燥または自然乾燥し、液状分散媒を揮散させることで塗膜を形成する。強制乾燥する方法としては熱風乾燥法や赤外線輻射法が採用できる。強制乾燥するときの加熱温度は、50℃〜100℃であり、汚染防止層の厚さは、0.01〜10μm、特に0.05〜2.0μmの範囲にあるのが好適である。架橋剤を用いる場合は、乾燥後に常温〜120℃で数分〜数日間、より好ましくは50℃〜80℃で1日〜3日間の熟成をすることにより十分性能が発揮される。
また、本発明の汚染防止シートは、汚染防止層の水に対する接触角が、20度以下であることが好ましい。
The antifouling paint according to the present invention is applied to the surface of an article, forcedly dried or naturally dried, and a liquid dispersion medium is volatilized to form a coating film. As a forced drying method, a hot air drying method or an infrared radiation method can be employed. The heating temperature for forced drying is 50 ° C. to 100 ° C., and the thickness of the contamination prevention layer is preferably in the range of 0.01 to 10 μm, particularly 0.05 to 2.0 μm. In the case of using a crosslinking agent, sufficient performance is exhibited by aging at room temperature to 120 ° C. for several minutes to several days, more preferably 50 ° C. to 80 ° C. for 1 day to 3 days after drying.
Moreover, it is preferable that the contact angle with respect to the water of a pollution prevention layer is 20 degrees or less.
本発明によれば、汚染防止性、親水性、結露防止性、帯電防止性、密着性、高硬度、機械的強度、耐擦傷性、耐摩耗性、耐光性、耐熱性、耐溶剤性、耐薬品性、耐汚染性に優れた塗膜を与える塗料が提供される。該塗料は、汚染防止機能を目的とするプラスチック用塗料、ガラス用塗料、建材用塗料、車輌用塗料、電子機器用塗料などとして有用である。 According to the present invention, contamination resistance, hydrophilicity, anti-condensation, antistatic properties, adhesion, high hardness, mechanical strength, scratch resistance, abrasion resistance, light resistance, heat resistance, solvent resistance, solvent resistance Provided is a paint that provides a coating film excellent in chemical resistance and stain resistance. The paint is useful as a paint for plastics, a paint for glass, a paint for building materials, a paint for vehicles, a paint for electronic devices, etc. for the purpose of preventing contamination.
次に実施例および比較例を挙げて本発明をさらに具体的に説明するが、本発明はこれらの実施例などに限定されるものではない。なお、以下の例における「部」および「%」は特に断りのない限り質量基準である。 EXAMPLES Next, although an Example and a comparative example are given and this invention is demonstrated further more concretely, this invention is not limited to these Examples. In the following examples, “parts” and “%” are based on mass unless otherwise specified.
実施例1
コロイダルシリカゾル(商品名MKCシリケートMSH6、三菱化学(株)製、シリカ含有量6.0%、コロイダルシリカの平均粒子径1〜100nm)100部に、高速ディスパーで撹拌しながら、予め溶解しておいたポリビニルアルコール(商品名PVA−217、クラレ(株)製、ケン化度88%、平均重合度1,700)の10%水溶液10.6部を15分かけてゆっくり加え、さらに30分撹拌し、本発明の汚染防止塗料を得た。該汚染防止塗料をポリエチレンテレフタレート(以下「PET」と記す)フィルム上に乾燥汚染防止層が1.0μmの厚さになるように塗布し、120℃のオーブンで2分間乾燥し、本発明の汚染防止性フィルムを得た。
Example 1
In 100 parts of colloidal silica sol (trade name: MKC silicate MSH6, manufactured by Mitsubishi Chemical Corporation, silica content: 6.0%, average particle diameter of colloidal silica of 1 to 100 nm), it is dissolved in advance while stirring with a high-speed disper. 10.6 parts of 10% aqueous solution of polyvinyl alcohol (trade name PVA-217, manufactured by Kuraray Co., Ltd., saponification degree 88%, average polymerization degree 1,700) was slowly added over 15 minutes, and further stirred for 30 minutes. Thus, the antifouling paint of the present invention was obtained. The antifouling paint is applied on a polyethylene terephthalate (hereinafter referred to as “PET”) film so that the dry antifouling layer has a thickness of 1.0 μm, and dried in an oven at 120 ° C. for 2 minutes to obtain the contamination of the invention. A protective film was obtained.
実施例2
実施例1のポリビニルアルコールに代えて、ポリビニルアルコール(商品名PVA−117、クラレ(株)製、ケン化度98.5%、平均重合度1,700)を使用した以外は実施例1と同様にして本発明の汚染防止塗料および膜厚が1.0μmの汚染防止性フィルムを得た。
Example 2
It replaces with the polyvinyl alcohol of Example 1, and uses polyvinyl alcohol (Brand name PVA-117, the Kuraray Co., Ltd. make, saponification degree 98.5%, average degree of polymerization 1,700), and is the same as Example 1. Thus, the antifouling paint of the present invention and the antifouling film having a film thickness of 1.0 μm were obtained.
実施例3
実施例1のポリビニルアルコールに代えて、ポリビニルアルコール(商品名PVA−205、クラレ(株)製、ケン化度88%、平均重合度500)を使用した以外は実施例1と同様にして本発明の汚染防止塗料および膜厚が1.0μmの汚染防止性フィルムを得た。
Example 3
The present invention was carried out in the same manner as in Example 1 except that polyvinyl alcohol (trade name PVA-205, manufactured by Kuraray Co., Ltd., saponification degree 88%, average polymerization degree 500) was used in place of the polyvinyl alcohol of Example 1. The antifouling paint and the antifouling film having a film thickness of 1.0 μm were obtained.
実施例4
実施例1のポリビニルアルコールに代えて、アクリルポリマー水溶液(商品名ジョンクリル501、ジョンソンポリマー(株)製、固形分29.5%)3.6部を使用した以外は実施例1と同様にして本発明の汚染防止塗料および膜厚が1.0μmの汚染防止性フィルムを得た。
Example 4
It replaced with the polyvinyl alcohol of Example 1, and carried out similarly to Example 1 except having used 3.6 parts of acrylic polymer aqueous solution (Brand name John Krill 501 and Johnson polymer Co., Ltd. product, solid content 29.5%). The antifouling paint of the present invention and the antifouling film having a film thickness of 1.0 μm were obtained.
実施例5
実施例1のポリビニルアルコール水溶液の使用量を40.0部とした以外は実施例1と同様にして本発明の汚染防止塗料および膜厚が1.0μmの汚染防止性フィルムを得た。
Example 5
Except that the amount of the polyvinyl alcohol aqueous solution used in Example 1 was 40.0 parts, the antifouling paint of the present invention and the antifouling film having a film thickness of 1.0 μm were obtained in the same manner as Example 1.
実施例6
実施例5の汚染防止塗料に架橋剤である水分散イソシアネート(商品名デュラネートWB40−100、旭化成ケミカルズ社製)0.05部を添加し、50℃で3日キュアーしたこと以外は実施例1と同様にして本発明の汚染防止塗料および膜厚が1.0μmの汚染防止性フィルムを得た。
Example 6
Example 1 except that 0.05 parts of water-dispersed isocyanate (trade name Duranate WB40-100, manufactured by Asahi Kasei Chemicals) as a crosslinking agent was added to the antifouling paint of Example 5 and cured at 50 ° C. for 3 days. Similarly, the antifouling paint of the present invention and the antifouling film having a film thickness of 1.0 μm were obtained.
比較例1
実施例1のポリビニルアルコールに代えて、アクリルエマルジョン(商品名ジョンクリル741、ジョンソンポリマー(株)製、固形分49%)2.2部を使用した以外は実施例1と同様にして比較例の汚染防止塗料および膜厚が1.0μmの汚染防止性フィルムを得た。
Comparative Example 1
A comparative example was prepared in the same manner as in Example 1 except that 2.2 parts of an acrylic emulsion (trade name John Krill 741, manufactured by Johnson Polymer Co., Ltd., solid content 49%) was used in place of the polyvinyl alcohol of Example 1. An antifouling paint and an antifouling film having a thickness of 1.0 μm were obtained.
比較例2
エチルシリケート(商品名エチルシリケート40、コルコート社製)0.3部とシランカップリング剤(商品名SH6040、東レダウコーニング社製)0.46部、2N塩酸0.01部、アルミニウムイソプロポキシド0.05部、35%塩酸0.04部、水0.09部、エタノール0.40部、N,N−ジメチルベンジルアミン0.01部を加えて25℃で10分間撹拌して得られた溶液に25%ポリアクリル酸水溶液(数平均分子量130,000)20.40部とメタノール78.60部を混合して得られた溶液を添加し、25℃で2分間撹拌して透明な汚染防止塗料を得た。この汚染防止塗料をPETフィルム上に乾燥汚染防止層が4.0μmの厚さになるように塗布しオーブンで150℃で10分間乾燥して比較例の汚染防止性フィルムを得た。
Comparative Example 2
Ethyl silicate (trade name ethyl silicate 40, manufactured by Colcoat Co.) 0.3 part and silane coupling agent (trade name SH 6040, manufactured by Toray Dow Corning Co., Ltd.) 0.46 part, 2N hydrochloric acid 0.01 part,
試験例
上記で得られた実施例および比較例の汚染防止塗料および汚染防止性フィルムの性能を以下の項目について試験し、表1の結果を得た。
<造膜性>
汚染防止塗料をフィルムに塗布および乾燥後、得られた汚染防止層のクラックを目視で観察した。
クラックがない:○
クラックがある:×
Test Example The performance of the antifouling paints and antifouling films of Examples and Comparative Examples obtained above was tested on the following items, and the results shown in Table 1 were obtained.
<Film-forming properties>
After the antifouling paint was applied to the film and dried, the resulting antifouling layer was visually observed for cracks.
No cracks: ○
There is a crack: ×
<透明性>
スガ試験機(株)製直読ヘーズコンピューターHGM−2DPを使用し、汚染防止性フィルムのヘイズ値を測定した。
ヘイズ値=測定値−基材のヘイズ値
ヘイズ値が1.0未満:○
ヘイズ値が1.0〜5.0未満:△
ヘイズ値が5.0以上:×
<Transparency>
Using a direct reading haze computer HGM-2DP manufactured by Suga Test Instruments Co., Ltd., the haze value of the antifouling film was measured.
Haze value = Measured value−Haze value of substrate Haze value is less than 1.0: ○
A haze value of 1.0 to less than 5.0: Δ
Haze value is 5.0 or more: ×
<汚染防止性>
東京都地区で1年間屋外曝露後の試験片と初期試験片の外観を目視にて観察した。
初期試験片と比較し外観の変化がない:○
塗膜に汚れがやや確認された:△
塗膜の汚染が著しい:×
<Pollution prevention>
The appearance of the test piece and the initial test piece after outdoor exposure for one year in the Tokyo area was visually observed.
No change in appearance compared to initial test piece: ○
The coating film was slightly dirty: △
Significant contamination of the coating film: ×
<耐光性>
サンシャインウェザオメーター試験(温度:83℃、水無、200時間)後、外観の変化を目視にて観察した。
初期試験片と比較し外観の変化がない:○
塗膜の光沢性がやや低下した:△
塗膜に光沢の低下、亀裂が見られた:×
<Light resistance>
After the sunshine weatherometer test (temperature: 83 ° C., no water, 200 hours), the change in appearance was visually observed.
No change in appearance compared to initial test piece: ○
The gloss of the coating film was slightly lowered:
The coating film showed a decrease in gloss and cracks: ×
<接触角>
協和界面科学(株)製接触角計CA−A型を使用し、水滴を0.01mlにして汚染防止性フィルムの汚染防止層面に接触させ、1分後に20℃で測定を行った。
<Contact angle>
Using a contact angle meter CA-A type manufactured by Kyowa Interface Science Co., Ltd., water droplets were made 0.01 ml and contacted with the antifouling layer surface of the antifouling film, and measurement was performed at 20 ° C. after 1 minute.
<耐水性>
汚染防止性フィルムの汚染防止層面に40℃の温水を滴下し、荷重100gをかけてラビング試験を行って、汚染防止層が剥離した回数で評価した。
ラビング回数10回未満:×
ラビング回数10回〜19回未満:△
ラビング回数19回以上:○
<Water resistance>
40 degreeC warm water was dripped at the pollution prevention layer surface of the pollution prevention film, the load 100g was applied, the rubbing test was done, and it evaluated by the frequency | count that the pollution prevention layer peeled.
Less than 10 rubbing times: ×
Number of rubbing times 10 to less than 19: △
More than 19 rubbing times: ○
<耐温水性>
汚染防止性フィルムを80℃の温水に2分間浸漬した後、表面の水分を拭き取り汚染防止層の変化を観察した。
まったく変化なし:◎
ほとんど変化なし:○
僅かに変化あり:△
かなり変化あり:×
<Hot water resistance>
After immersing the antifouling film in warm water at 80 ° C. for 2 minutes, the moisture on the surface was wiped off and the change of the antifouling layer was observed.
No change at all: ◎
Almost no change: ○
Slight change: △
There is considerable change: ×
<密着性>
汚染防止性フィルムの汚染防止層と基材PETフィルムとの接着性を碁盤目試験(セロハンテープ剥離クロスカット法)にて行った。
剥離していない升目が95%以上:◎
剥離していない升目が95%未満〜70%:○
剥離していない升目が70%未満〜40%:△
剥離していない升目が40%未満:×
<Adhesion>
The adhesion between the antifouling layer of the antifouling film and the base PET film was determined by a cross cut test (cellophane tape peeling cross-cut method).
95% or more of non-peeled cells: ◎
Less than 95% to 70% of non-peeled cells: ○
Less than 70% to 40% of non-peeled cells:
Less than 40% of non-peeled cells: ×
<耐傷付性>
汚染防止性フィルムの汚染防止層面を約10g/cm2の荷重にてスコッチブライト(住友スリーエム(株)製)で擦り、表面の傷付きを目視にて確認した。
確認できる傷が0〜5本:○
確認できる傷が6〜10本:△
確認できる傷が11本以上:×
<Scratch resistance>
The antifouling film surface of the antifouling film was rubbed with Scotch Bright (manufactured by Sumitomo 3M Co., Ltd.) under a load of about 10 g / cm 2 to visually check the surface for scratches.
0 to 5 scratches that can be confirmed: ○
6-10 scratches that can be confirmed: △
11 or more scratches that can be confirmed: ×
以上のように本発明の汚染防止塗料は高度な汚染防止性能を示し、従来の汚染防止塗料に比べて優れた耐久性を示す。さらに、本発明の汚染防止塗料は簡易な方法で製造が可能であり工業的に非常に有用である。 As described above, the antifouling paint of the present invention exhibits a high level of antifouling performance, and exhibits superior durability compared to conventional antifouling paints. Further, the antifouling paint of the present invention can be produced by a simple method and is very useful industrially.
Claims (12)
An antifouling sheet characterized in that the antifouling paint according to any one of claims 1 to 8 is applied to one surface of a substrate sheet, and an antifouling layer is formed at a temperature of room temperature to 120 ° C. Production method.
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JP2015140271A (en) * | 2014-01-28 | 2015-08-03 | 日揮触媒化成株式会社 | Hydrophobic silica powder and method of producing the same |
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CN110499053A (en) * | 2018-05-16 | 2019-11-26 | 骏能化工(龙南)有限公司 | A kind of water-based industrial paint multifunctional assistant |
JP7084082B1 (en) | 2021-06-24 | 2022-06-14 | 株式会社ミラクール | Structure containing hydrophilic coating composition and hydrophilic coating |
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JPS61155474A (en) * | 1984-12-28 | 1986-07-15 | Kansai Paint Co Ltd | Aqueous coating composition |
JPH0880474A (en) * | 1994-09-09 | 1996-03-26 | Kansai Paint Co Ltd | Coated steel sheet good in staining preventing property |
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JP2008127513A (en) * | 2006-11-24 | 2008-06-05 | Kikusui Chemical Industries Co Ltd | Hydrophilic inorganic paint |
CN101376616B (en) * | 2008-09-25 | 2011-03-23 | 烟台五洲施得富肥料有限公司 | Production method of sol sodium silicate mixture endoplasm sustained release agent |
JP2011195983A (en) * | 2010-03-18 | 2011-10-06 | Duplo Seiko Corp | Apparatus for producing recycled pulp and apparatus for recycling-treatment of waste paper |
JP2012210605A (en) * | 2011-03-31 | 2012-11-01 | Dainippon Toryo Co Ltd | Hydrophilicity antifouling treatment method of building outer wall face, and building |
JP2013256090A (en) * | 2012-06-14 | 2013-12-26 | Toppan Printing Co Ltd | Antifouling film and production method therefor |
JP2014070138A (en) * | 2012-09-28 | 2014-04-21 | Dainippon Toryo Co Ltd | Composition for forming hydrophilic coating film, and hydrophilic coating film |
JP2015140271A (en) * | 2014-01-28 | 2015-08-03 | 日揮触媒化成株式会社 | Hydrophobic silica powder and method of producing the same |
WO2019064973A1 (en) * | 2017-09-29 | 2019-04-04 | 富士フイルム株式会社 | Anti-fogging layer laminate |
JPWO2019064973A1 (en) * | 2017-09-29 | 2020-04-02 | 富士フイルム株式会社 | Anti-fog layer laminate |
CN110499053A (en) * | 2018-05-16 | 2019-11-26 | 骏能化工(龙南)有限公司 | A kind of water-based industrial paint multifunctional assistant |
JP7084082B1 (en) | 2021-06-24 | 2022-06-14 | 株式会社ミラクール | Structure containing hydrophilic coating composition and hydrophilic coating |
WO2022270472A1 (en) * | 2021-06-24 | 2022-12-29 | 株式会社ミラクール | Composition for hydrophilic coating, and structure including hydrophilic coating |
JP2023004820A (en) * | 2021-06-24 | 2023-01-17 | 株式会社ミラクール | Composition for hydrophilic coating and structure comprising hydrophilic coating |
CN116769366A (en) * | 2023-06-14 | 2023-09-19 | 西安长大力创交通科技有限公司 | Preparation method of coating for preventing adhesion of dirt in highway environment |
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