JP2000262367A - Antifogging mirror and its production - Google Patents

Antifogging mirror and its production

Info

Publication number
JP2000262367A
JP2000262367A JP11071234A JP7123499A JP2000262367A JP 2000262367 A JP2000262367 A JP 2000262367A JP 11071234 A JP11071234 A JP 11071234A JP 7123499 A JP7123499 A JP 7123499A JP 2000262367 A JP2000262367 A JP 2000262367A
Authority
JP
Japan
Prior art keywords
mirror
film
metal oxide
water
coating
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.)
Pending
Application number
JP11071234A
Other languages
Japanese (ja)
Inventor
Seiji Yamazaki
誠司 山崎
Hideki Yamamoto
秀樹 山本
Yoshihiro Nishida
佳弘 西田
Keiji Honjo
啓司 本城
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Central Glass Co Ltd
Original Assignee
Central Glass Co Ltd
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 Central Glass Co Ltd filed Critical Central Glass Co Ltd
Priority to JP11071234A priority Critical patent/JP2000262367A/en
Publication of JP2000262367A publication Critical patent/JP2000262367A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/36Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
    • C03C17/3602Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
    • C03C17/3657Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating having optical properties
    • C03C17/3663Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating having optical properties specially adapted for use as mirrors
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/006Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
    • C03C17/007Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character containing a dispersed phase, e.g. particles, fibres or flakes, in a continuous phase
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/36Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/40Coatings comprising at least one inhomogeneous layer
    • C03C2217/43Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
    • C03C2217/44Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the composition of the continuous phase
    • C03C2217/45Inorganic continuous phases
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/40Coatings comprising at least one inhomogeneous layer
    • C03C2217/43Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
    • C03C2217/46Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/70Properties of coatings
    • C03C2217/77Coatings having a rough surface
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/70Properties of coatings
    • C03C2217/78Coatings specially designed to be durable, e.g. scratch-resistant
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2218/00Methods for coating glass
    • C03C2218/30Aspects of methods for coating glass not covered above
    • C03C2218/365Coating different sides of a glass substrate

Abstract

PROBLEM TO BE SOLVED: To extremely improve an antifogging property by coating the opposite side surface of a mirror subjected to a mirror finishing surface treatment on one surface of a substrate with a metal oxide film having a rugged shape on the surface uniformly dispersed with specific weight % of water absorptive particulates in a metal oxide for matrix formation and specifying the cloud value of this film. SOLUTION: An antifogging mirror is formed by coating the one side surface of the substrate with the metal oxide film, into which 10 to 30 wt.% superfine particles having a cloud value of >=1 to <=20% are incorporated, and subjecting the surface on the other side to the mirror finishing surface treatment. The representative process for production consists in uniformly mixing the water absorptive particulates, raw material for the metal oxide for matrix formation and a solvent, applying the solution prepared in this manner on the opposite side surface of the mirror subjected to the mirror finishing surface treatment on the one surface side of the substrate, then baking the coating to fix the metal oxide film, thereby producing the mirror. As a result, the antifogging mirror which is capable of maintaining the excellent antifogging property for a long period of time in spite of repetitive use, is highly durable and is free of problems in practicable use in wear resistance and chemical resistance.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、主として浴室用の
鏡に用いられる防曇鏡に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an anti-fog mirror mainly used for bathroom mirrors.

【0002】[0002]

【従来の技術】最近、基材に親水性、防曇性または防汚
性を付与するために基材の表面に光触媒機能を有する被
膜を形成することが行われている。例えば、特開平5ー
253544号公報に記載のアナターゼ型チタニアを主
体とする光触媒微粉末をその一部がバインダ層表面から
露出するようにした板状部材、特開平7−232080
号公報に記載の光触媒微粒子がチタニア、酸化亜鉛、チ
タン酸ストロンチウム、酸化鉄、酸化タングステン、チ
タン酸鉄、酸化ビスマス、酸化錫等であり、光触媒粒子
の間隙充填粒子が錫、チタン、銀、銅、亜鉛、鉄、白
金、コバルト、ニッケルの金属または酸化物である光触
媒機能を有する多機能材、特開平9−59042号公報
記載の光触媒性の平均結晶粒子径が約0.1μm以下の
チタニアの粒子を含有する親水性被膜で覆われた透明基
材等が知られている。
2. Description of the Related Art Recently, a film having a photocatalytic function has been formed on the surface of a substrate in order to impart hydrophilicity, antifogging property or antifouling property to the substrate. For example, a plate-like member in which a photocatalyst fine powder mainly composed of anatase type titania described in JP-A-5-253544 is partially exposed from the surface of the binder layer is disclosed in JP-A-7-23080.
The photocatalyst fine particles described in the publication are titania, zinc oxide, strontium titanate, iron oxide, tungsten oxide, iron titanate, bismuth oxide, tin oxide and the like, and the gap filling particles of the photocatalyst particles are tin, titanium, silver, and copper. A multifunctional material having a photocatalytic function, which is a metal or oxide of zinc, iron, platinum, cobalt, nickel, or titania having a photocatalytic average crystal particle diameter of about 0.1 μm or less described in JP-A-9-59042. Transparent substrates and the like covered with a hydrophilic coating containing particles are known.

【0003】また従来、界面活性剤を基材表面に塗布す
ることで表面を親水性に改質することは古くから知られ
ており、界面活性剤にポリアクリル酸やポリビニルアル
コールなどの水溶性有機高分子を添加・配合すること
で、親水性の持続性を上げることが知られている(特開
昭52−101680号公報等)。
Conventionally, it has been known for a long time that a surfactant is applied to the surface of a base material to modify the surface to be hydrophilic, and a water-soluble organic solvent such as polyacrylic acid or polyvinyl alcohol is used as the surfactant. It is known that the persistence of hydrophilicity is increased by adding and blending a polymer (Japanese Patent Application Laid-Open No. 52-101680).

【0004】さらに、疎水性ポリマーよりなる多孔質膜
の表面および内部にポリビニルアルコールと酢酸ビニル
の共重合体の被膜を介して、セルロースやグリコール類
およびグリセリンなどの親水性ポリマーを被膜固定化す
る方法が知られている(特公平5ー67330号公報
等)。
Further, a method of immobilizing a hydrophilic polymer such as cellulose, glycols and glycerin on the surface and inside of a porous membrane made of a hydrophobic polymer through a coating of a copolymer of polyvinyl alcohol and vinyl acetate. Is known (Japanese Patent Publication No. 5-67330).

【0005】またさらに、物理的方法では、プラズマ処
理、レーザー照射処理などの親水化処理が実用化されて
いる。
Further, in the physical method, a hydrophilic treatment such as a plasma treatment and a laser irradiation treatment has been put to practical use.

【0006】さらに、化学的方法には、表面にラジカル
を発生させ親水性の残基を有する重合性化合物をグラフ
ト重合させる方法や、酸、塩基性物質などの表面の結合
を切断し、親水性の残基に変化させる方法などが行われ
ている。
Further, chemical methods include a method of generating radicals on the surface and graft-polymerizing a polymerizable compound having a hydrophilic residue, and a method of cutting a bond of a surface such as an acid or a basic substance to obtain a hydrophilic compound. And the like.

【0007】[0007]

【発明が解決しようとする課題】上記の光触媒機能を利
用した親水性および防曇性においては、紫外線が当たる
ことが必須であり、紫外線が当たらない浴室において
は、親水性および防曇性は極めて困難である。そのため
浴室の鏡に紫外線が当たるように新たに光源を設置する
必要がある。また紫外線が当たって一旦親水性および防
曇性となった表面であっても、その性能を維持できるの
は短時間であり、数時間後には失われる。したがって頻
繁に紫外線を照射するなどの操作が必要となる。さらに
防曇性を発現するには、一義的に水の接触角だけで限定
されるものではないが、一般に防曇性となる場合の水の
接触角は5#以下で、10#付近では防曇性は失われる。
また光触媒膜を基材に被覆した場合、光触媒機能を発現
するチタニアは高屈折率膜であるため反射率が高くなっ
たり着色し、特に鏡においては裏面側が鏡面処理されて
いるため、二重像が発生し鏡としての本来の機能を損な
ったり、意匠性を損なう場合もある。
In the above-mentioned hydrophilicity and anti-fogging property utilizing the photocatalytic function, it is essential to irradiate with ultraviolet rays, and in a bathroom without irradiating ultraviolet rays, the hydrophilicity and anti-fogging property are extremely high. Have difficulty. Therefore, it is necessary to newly install a light source so that the mirror in the bathroom is irradiated with ultraviolet rays. In addition, even if the surface is once hydrophilic and anti-fog when exposed to ultraviolet light, its performance can be maintained for a short time, and is lost after several hours. Therefore, it is necessary to frequently perform operations such as irradiation with ultraviolet rays. In order to further exhibit anti-fogging properties, it is not limited solely to the water contact angle. Fogging is lost.
In addition, when a photocatalytic film is coated on a substrate, titania exhibiting a photocatalytic function is a high-refractive-index film and thus has high reflectivity and is colored. May occur, impairing the original function as a mirror or impairing the design.

【0008】一方、物理的な処理による防曇性も短期的
にしか効果を維持することができず、またポリエチレン
オキシド系有機ポリマー膜では、耐水性や機械的強度が
低いために用途によっては実用上十分なものとは言えな
い。
On the other hand, the antifogging property by physical treatment can be maintained only for a short period of time, and the polyethylene oxide organic polymer film has low water resistance and low mechanical strength, so that it may be practically used depending on the application. Not enough.

【0009】また、例えば多孔質膜の表面および内部に
ポリビニルアルコールと酢酸ビニルの共重合体の被膜を
介してセルロースなどの被膜を固定化する方法において
も、被膜は極めて柔らかいものであり、しかも化学的耐
久性も期待でき難いものであり、使用する用途が限定さ
れる。
Also, for example, in a method of immobilizing a film such as cellulose on the surface and the inside of a porous film via a film of a copolymer of polyvinyl alcohol and vinyl acetate, the film is extremely soft, It is also difficult to expect good durability, and the use to be used is limited.

【0010】さらに、例えば無機物質からなる被膜は、
膜の強度は比較的高いが親水性を呈する物質は水に対す
る溶解性も高く被膜は容易に消失するもので、実用上そ
の用途は限られたものとなる。
Further, for example, a coating made of an inorganic substance
Substances having relatively high film strength but exhibiting hydrophilicity have high solubility in water and the coating easily disappears, which limits the practical use thereof.

【0011】また、例えば防曇鏡としてはヒーター内蔵
式がすでに商品化されているが、この場合も瞬時に曇り
が晴れるものではなく、スイッチを入れてから曇りが晴
れるまでに数分間かかり、またコストも高いために汎用
性があるとは言い難いものである。
For example, as an anti-fog mirror, a type with a built-in heater has already been commercialized, but also in this case, the fogging does not clear instantaneously, and it takes several minutes after the switch is turned on until the fogging clears. It is hard to say that it has versatility because of its high cost.

【0012】以上のこれらの方法は、いずれの方法も一
時的もしくは比較的短時間の間だけ防曇性を付与するも
ので、防曇効果の十分な持続性は期待し難いばかりでな
く、またコスト高となり実用化においては採用が困難な
ものであった。
[0012] In each of the above methods, the antifogging property is imparted only temporarily or for a relatively short period of time, and it is difficult to expect sufficient durability of the antifogging effect. The cost was high and it was difficult to adopt it for practical use.

【0013】[0013]

【課題を解決するための手段】本発明は、従来のこのよ
うな事情に鑑みてなされたものであって、金属酸化物膜
を鏡の表面に形成し(反対側が鏡面)、且つ金属酸化物
膜のマトリックス中には吸水性超微粒子が均一に分散さ
れており、一旦水に濡れるとヘーズが解消され透明性と
なり、また図1に示す組織との相乗効果により優れた保
水性も付与されるため、例えば浴室内の高い相対湿度の
環境下での使用では、極めて防曇性に優れる防曇鏡およ
びその製造方法を提供するものである。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and has been made in consideration of the above-described circumstances, and has a metal oxide film formed on a surface of a mirror (an opposite side is a mirror surface). The water-absorbing ultrafine particles are evenly dispersed in the matrix of the membrane, and once wetted with water, the haze is eliminated and the film becomes transparent, and also excellent water retention is provided by a synergistic effect with the structure shown in FIG. Therefore, for example, when used in an environment with a high relative humidity in a bathroom, the present invention provides an antifogging mirror having extremely excellent antifogging properties and a method for manufacturing the same.

【0014】すなわち、本発明の防曇鏡は、基板の片面
に鏡面処理が施されている鏡の反対側表面に、マトリッ
クス形成用金属酸化物中に10〜30重量%の吸水性超
微粒子が均一に分散された表面が凹凸形状を有する金属
酸化物膜が被覆され、且つ該膜の曇価が1%〜20%で
あることを特徴とする。
That is, in the antifogging mirror of the present invention, 10 to 30% by weight of water-absorbing ultrafine particles in a metal oxide for forming a matrix is provided on the opposite surface of the mirror having one surface of the substrate subjected to mirror finishing. A metal oxide film having a uniformly dispersed surface with an uneven shape is coated, and the haze of the film is 1% to 20%.

【0015】また、金属酸化物被膜が被覆された透明基
板の可視光線透過率は80%〜94%であることが好ま
しい。
The visible light transmittance of the transparent substrate coated with the metal oxide film is preferably 80% to 94%.

【0016】またさらに、本発明の防曇鏡は、浴室用の
紫外線なしで水に濡れた状態で防曇性を持続し、二重像
を形成しないことができる。
Further, the anti-fog mirror of the present invention can maintain the anti-fog property in a state of being wetted by water without ultraviolet rays for a bathroom, and can not form a double image.

【0017】また、本発明の防曇鏡の製造方法は、吸水
性微粒子、マトリックス形成用金属酸化物用原料、およ
び溶媒とを均一に混合し調整した溶液を、基板の片側面
に鏡面処理が施こされてなる鏡の反対側表面に塗布した
後、焼成して金属酸化物膜を固着させることを特徴とす
る。
Further, in the method for manufacturing an anti-fog mirror according to the present invention, a solution prepared by uniformly mixing water-absorbing fine particles, a raw material for a metal oxide for forming a matrix, and a solvent is subjected to mirror finishing on one side of a substrate. The method is characterized in that a metal oxide film is fixed after being applied to the opposite surface of the mirror to be applied and then baked.

【0018】[0018]

【発明の実施の形態】本発明の防曇鏡は、基板の片側表
面に、曇価が1%以上20%以下である超微粒子が10
〜30重量%含有された金属酸化物膜が被覆され、他面
側の表面は鏡面処理がなされたものであり、代表的な製
造方法としては、吸水性微粒子、マトリックス形成用金
属酸化物用原料、および溶媒とを均一に混合し調整した
溶液を、基板の片側面に鏡面処理が施こされてなる鏡の
反対側表面に塗布した後、焼成して金属酸化物膜を固着
させて製造することができる。
BEST MODE FOR CARRYING OUT THE INVENTION In the anti-fog mirror of the present invention, ultrafine particles having a haze of 1% or more and 20% or less are formed on one surface of a substrate.
3030% by weight of a metal oxide film, and the other surface is mirror-finished. Typical manufacturing methods include water-absorbing fine particles and a raw material for a metal oxide for forming a matrix. , And a solvent prepared by uniformly mixing the solvent with the solution, and then applying the solution to the opposite surface of the mirror, which has been subjected to mirror finishing on one side of the substrate, and then sintering to fix the metal oxide film. be able to.

【0019】金属酸化物膜としては、マトリックス形成
用金属酸化物中に吸水性超微粒子が均一に分散されたも
のであり、該マトリックス形成用金属酸化物の主な原料
としては、例えばシリカの主な原料としては、金属アル
コキド類では、シリカアルコキシド類が、テトラエトキ
シシラン、テトラメトキシシラン、モノメチルトリエト
キシシラン、モノメチルトリメトキシシラン、ジメチル
ジメトキシシラン、ジメチルジエトキシシラン、その他
のテトラアルコキシシラン化合物、その他のアルキルア
ルコキシシラン化合物、また、チタニアの主な原料とし
ては、テトライソプロポキシチタン、テトラノルマルブ
トキシチタン、トリイソプロポキシチタンモノアセチル
アセトナート等のアルコキシド類、アルミナの主な原料
としては、アルコキシド類では、アルミニウムブトキシ
ド、アルミアセテート類では、アルミニウムアセチルア
セトナート等の有機金属化合物、ジルコニアの主な原料
としては、アルコキシド類では、ジルコニウムブトキシ
ド、ジルコニアアセテート類では、ジ ルコニウムアセ
チルアセトナート等の有機金属化合物を用いることがで
きる。
The metal oxide film is formed by uniformly dispersing water-absorbing ultrafine particles in a metal oxide for forming a matrix. The main raw material of the metal oxide for forming a matrix is, for example, a main material of silica. As raw materials, metal alkoxides, silica alkoxides, tetraethoxysilane, tetramethoxysilane, monomethyltriethoxysilane, monomethyltrimethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, other tetraalkoxysilane compounds, other Alkoxysilane compounds of the above, the main raw materials of titania include alkoxides such as tetraisopropoxytitanium, tetranormal butoxytitanium, triisopropoxytitanium monoacetylacetonate, and the main raw materials of alumina include alcohol In the case of SIDs, aluminum butoxide, in the case of aluminum acetates, there are organometallic compounds such as aluminum acetylacetonate, and in the main raw materials of zirconia, in the case of alkoxides, there are zirconium butoxide; in the case of zirconia acetates, such as zirconium acetylacetonate. Organometallic compounds can be used.

【0020】また、吸水性超微粒子としては、例えばシ
リカとしては、結晶性のシリカまたは無定型、ガラス状
もしくはコロイダルシリカのいずれであってもよいが特
にコロイダルシリカが好ましく、吸湿性のアルミナ微粒
子としては、ベーマイト型結晶のアルミナが好ましい。
またチタニア微粒子としてはアナターゼ、ルチルなどの
結晶質あるいはコロイド状非晶質であってもよいが、特
に結晶性微粒子が好ましい。なお吸水性超微粒子とは、
特に粒径を限定するものではないが、粒径が50nm以
下であるものが特に好ましい。
As the water-absorbing ultrafine particles, for example, the silica may be crystalline silica or amorphous, glassy or colloidal silica, but colloidal silica is particularly preferred. Is preferably alumina of boehmite type crystal.
The titania fine particles may be crystalline or colloidal amorphous such as anatase or rutile, but crystalline fine particles are particularly preferable. The superabsorbent ultrafine particles are
The particle size is not particularly limited, but those having a particle size of 50 nm or less are particularly preferred.

【0021】前記希釈溶媒としては、アルコ−ル系溶媒
が好ましく、具体例としては、メタノ−ル、エタノ−
ル、プロパノ−ル、ブタノ−ル、エチレングリコ−ル、
プロピレングリコール、ブチレングリコール、ペンチレ
ングリコール、ヘキシレングリコ−ル、さらには酢酸エ
チル、酢酸ブチル、酢酸アミルなどのエステル類、さら
にはメチルセロソルブ、エチルセロソルブ、ブチルセロ
ソルブなどのセロソルブ類及びこれらを混合した溶媒
で、レベリング剤としてジメチルシリコーンなどのメチ
ルシリコーン類やフッ素系レベリング剤を適量加えても
良い。本来溶液中に含まれるアルコ−ル系やセロソルブ
系のもの単独または混合物を、該溶液の蒸発速度や被膜
粘度を勘案して選択すればよい。
The diluting solvent is preferably an alcoholic solvent, and specific examples thereof include methanol, ethanol and the like.
, Propanol, butanol, ethylene glycol,
Propylene glycol, butylene glycol, pentylene glycol, hexylene glycol, esters such as ethyl acetate, butyl acetate, and amyl acetate; and cellosolves such as methyl cellosolve, ethyl cellosolve, butyl cellosolve, and a mixture thereof. Then, an appropriate amount of a methyl silicone such as dimethyl silicone or a fluorine-based leveling agent may be added as a leveling agent. Alcohols or cellosolves which are originally contained in the solution may be selected alone or in a mixture in consideration of the evaporation rate of the solution and the film viscosity.

【0022】なお、前記金属酸化物膜を着色のないクリ
アのフロートガラスに形成した場合の可視光透過率は8
0%以上94%以下であることが好ましく、曇価(ヘー
ズ)は5%以上20%以下であることが好ましい。可視
光透過率が80%未満では、膜が水に濡れても透明性が
不足し、映像の鮮明さが不十分となり鏡としての機能が
十分あるとは言い難いものとなり、94%を超えると膜
のヘーズは1%未満となり、一旦水が濡れても水切れが
早く乾いた部分が曇る場合があり、防曇性が不十分とな
る。また、ヘーズが5%未満では可視光透過率の場合と
同様に、一旦水が濡れても水切れが早く乾いた部分が曇
る場合があり、防曇性が不十分となり、20%を超える
と水が濡れても透明性が不足し、映像の鮮明さが不十分
となり、鏡としての機能が十分であるとは言い難いもの
となる。なお、より好ましくは、可視光透過率は85〜
90%、曇価(ヘーズ)は8〜15%がよい。
When the metal oxide film is formed on clear float glass without coloring, the visible light transmittance is 8%.
The haze is preferably from 0% to 94%, and the haze is preferably from 5% to 20%. If the visible light transmittance is less than 80%, the transparency will be insufficient even if the film is wet with water, the image will be insufficiently clear, and it will be difficult to say that it has a sufficient mirror function. The haze of the film is less than 1%, and even when the film is once wet, the portion that dries quickly and becomes dry may become cloudy, and the antifogging property becomes insufficient. Further, if the haze is less than 5%, as in the case of the visible light transmittance, even if the water gets wet, the dried portion may quickly become dry and become cloudy, and the antifogging property may become insufficient. However, even if it gets wet, the transparency is insufficient, the sharpness of the image becomes insufficient, and the function as a mirror is hardly sufficient. In addition, more preferably, the visible light transmittance is 85 to 85.
The haze is preferably 90% and the haze is preferably 8% to 15%.

【0023】金属酸化物被膜中に含まれるマトリックス
形成用金属酸化物の含有比率は、該金属酸化物膜組成に
対して70〜90重量%であることが好ましく、90重
量%を超えると吸水性超微粒子の効果が十分に発揮され
ず、また膜の組織も図1に示すものとはなり難い。ま
た、70重量%未満では、膜の耐水性、耐薬品性などの
耐久性やの摩耗強度が低下し、浴室用鏡としての実用上
の採用が困難となるためである。
The content ratio of the metal oxide for forming a matrix contained in the metal oxide film is preferably from 70 to 90% by weight based on the composition of the metal oxide film. The effect of the ultrafine particles is not sufficiently exhibited, and the structure of the film is hardly as shown in FIG. On the other hand, if it is less than 70% by weight, the durability and abrasion strength of the film such as water resistance and chemical resistance are reduced, and it is difficult to practically use the film as a bathroom mirror.

【0024】被膜の膜厚は、特に限定されるものではな
いが、10〜400nmの範囲が好ましく、10nm未
満では一旦水を濡らすと濡れた直後は映像の歪みもなく
防曇性は良好であるが、浴室の高湿度下では膜の厚み方
向での吸水性が小さいために、水膜の厚みが不均一とな
り徐々に映像が歪み、鏡の機能としては不十分なものと
なる。400nmを超えると焼成時にクラックが発生し
やすくなるために、これを防止するために多段階の焼成
を必要とするなど生産性が悪くコストアップとなる。好
ましくは、150〜270nmの範囲で、より好ましく
は、180〜220nmの範囲である。
The thickness of the film is not particularly limited, but is preferably in the range of 10 to 400 nm, and if it is less than 10 nm, the image is not distorted immediately after wetting once with water and the anti-fog property is good. However, under high humidity in the bathroom, the water absorption in the thickness direction of the film is small, so that the thickness of the water film becomes uneven and the image is gradually distorted, and the function of the mirror becomes insufficient. If the thickness exceeds 400 nm, cracks are likely to occur during firing, so that multi-stage firing is required to prevent the cracks, resulting in poor productivity and increased cost. Preferably, it is in the range of 150 to 270 nm, more preferably in the range of 180 to 220 nm.

【0025】塗布液を基板上に塗布したのちの焼成温度
は、400〜600℃が好ましく、400℃未満では膜
の機械的強度ならびに耐酸、耐アルカリなど耐薬品性が
不十分であり、600℃を超えるとガラスが反ったり、
映像が歪んで鏡としての本来の機能を発揮できない。な
お、より好ましくは、500〜550℃の範囲である。
The baking temperature after coating the coating solution on the substrate is preferably 400 to 600 ° C. If it is less than 400 ° C., the mechanical strength of the film and the chemical resistance such as acid resistance and alkali resistance are insufficient. If it exceeds, the glass warps,
The image is distorted and the original function as a mirror cannot be exhibited. In addition, more preferably, it is the range of 500-550 degreeC.

【0026】塗布法としては、特に限定されるものでは
ないが、生産性などの面からは例えばスピンコート法あ
るいはディップコ−ト法、またリバ−スコ−ト法、フレ
キソ印刷法、その他のロールコート法、カーテンコート
法であり、さらにはノズルコ−ト法、スプレーコ−ト
法、バーコート法、スクリーン印刷法などが適宜採用し
得るものである。これら塗布法で塗布成膜する際の塗布
液中の全固形分濃度としては約0.1〜5重量%程度
で、塗布液粘度としては2〜10cp程度が好ましい。
The coating method is not particularly limited, but from the viewpoint of productivity and the like, for example, a spin coating method or a dip coating method, a reverse coating method, a flexographic printing method, and other roll coating methods. And a curtain coating method, and further, a nozzle coating method, a spray coating method, a bar coating method, a screen printing method and the like can be appropriately employed. The concentration of the total solid content in the coating liquid when forming a film by coating with these coating methods is preferably about 0.1 to 5% by weight, and the viscosity of the coating liquid is preferably about 2 to 10 cp.

【0027】塗布後の乾燥処理としては、乾燥温度が1
00〜200℃程度で乾燥時間が5〜30分間程度が好
ましく、より好ましくは、前記乾燥温度が140〜16
0℃程度で、乾燥時間が10〜20分間程度である。
As the drying treatment after the coating, the drying temperature is 1
The drying time is preferably about 00 to 200 ° C. and about 5 to 30 minutes, more preferably the drying temperature is 140 to 16
The drying time is about 10 to 20 minutes at about 0 ° C.

【0028】乾燥後の焼成処理としては、焼成温度が4
00〜600℃程度で焼成時間が1〜30分間程度が好
ましく、より好ましくは、前記焼成時間は5〜20分で
ある。
As the baking treatment after drying, a baking temperature of 4
The firing time at about 00 to 600 ° C. is preferably about 1 to 30 minutes, and more preferably the firing time is 5 to 20 minutes.

【0029】本発明に使用する基材としては、透明であ
れば特に限定するものではなく、ガラス、プラスチック
等を用いることができる。例えば、浴室用の鏡として
は、厚みが5.0mm程度のクリアのフロートガラスが
適当であるが、鏡の大きさ等により適宜選択して、使用
することができる。なお、浴室の環境条件は特に限定す
るものではないが、本発明の防曇鏡の機能をより有効に
発揮するためには、室温10〜40℃、湿度70〜95
%RHの環境が好ましい。
The substrate used in the present invention is not particularly limited as long as it is transparent, and glass, plastic and the like can be used. For example, as a bathroom mirror, clear float glass with a thickness of about 5.0 mm is suitable, but it can be appropriately selected and used depending on the size of the mirror and the like. In addition, although the environmental conditions of a bathroom are not specifically limited, In order to exhibit the function of the anti-fog mirror of this invention more effectively, room temperature 10-40 degreeC, humidity 70-95.
% RH environments are preferred.

【0030】また、金属酸化物膜の被覆は、鏡面処理が
施された鏡に行うことが好ましいが、場合によっては、
基板表面に金属酸化物膜を形成後、反対面に鏡面を施す
ことは差し支えない。
The coating of the metal oxide film is preferably carried out on a mirror which has been subjected to a mirror finish.
After forming the metal oxide film on the substrate surface, it is possible to form a mirror surface on the opposite surface.

【0031】[0031]

【作用】親水性ならびに防曇性に係わる物性は、膜表面
の水酸基の量と表面から内部に渡る保水性および水膜を
均一に形成できる膜表面形状への依存性が極めて高い。
つまり、膜表面と水の接触角が小さくできるだけ多くの
水を吸収または吸着し、この際に均一な水膜を形成でき
れば、親水効果ならびに防曇効果を長時間持続すること
が可能となる。本発明によって、ガラス基板上に形成さ
れた図1に示すような表面組織を有する金属酸化物膜
が、一旦水に濡れると長時間親水性ならびに防曇性を持
続できるのは、膜組織中には吸水性物質が分散されてお
り、これらは表面に水酸基を持っているため水と吸着し
やすく、また保水性も同時に発揮される。この効果と図
1に示す膜組織により、吸着した水は均一な水膜となり
水切れが起こりにくい。さらには、使用環境が高湿度下
の浴室であるために膜表面に吸着した水は脱離しにくい
ものとなるため、一旦水に濡らすと長時間防曇性を発揮
できるとともに、二重像もなく非常に鮮明に見える。ま
た、膜表面が均一な水膜で覆われているために油類等の
汚れも付きにくく防汚性も付与される。
The physical properties relating to hydrophilicity and anti-fogging property are extremely highly dependent on the amount of hydroxyl groups on the film surface, the water retention from the surface to the inside and the shape of the film surface capable of uniformly forming a water film.
That is, if the contact angle of water with the film surface is small and as much water as possible is absorbed or adsorbed and a uniform water film can be formed at this time, the hydrophilic effect and the antifogging effect can be maintained for a long time. According to the present invention, a metal oxide film formed on a glass substrate and having a surface texture as shown in FIG. 1 can maintain hydrophilicity and antifogging properties for a long time once it is wet with water because the film texture Are dispersed with water-absorbing substances. Since these have hydroxyl groups on their surface, they are easily adsorbed with water and also exhibit water retention. Due to this effect and the membrane structure shown in FIG. 1, the adsorbed water becomes a uniform water film, and the water does not easily run out. Furthermore, because the environment of use is a bathroom under high humidity, the water adsorbed on the membrane surface is difficult to desorb, so once wetted with water, it can exhibit anti-fog properties for a long time and there is no double image Looks very clear. In addition, since the film surface is covered with a uniform water film, dirt such as oils is hardly attached, and antifouling property is provided.

【0032】なお、親水性による防曇性を発現するに
は、一義的に水の接触角だけで限定されるものではない
が、一般に防曇性となる場合の水の接触角は5#以下で
あり、10#付近では防曇性は失われるため、本発明で
は、下記に示す親水性評価試験において、水の接触角が
5#以下を合格とした。
In order to exhibit the anti-fogging property due to hydrophilicity, it is not limited solely to the water contact angle. However, the contact angle of water when the anti-fogging property is obtained is generally 5 # or less. Since the antifogging property is lost around 10 #, in the present invention, a water contact angle of 5 # or less was accepted in the following hydrophilicity evaluation test.

【0033】[0033]

【実施例】以下、実施例により本発明を具体的に説明す
る。但し本発明はこれらの実施例に限定されるものでは
ない。
The present invention will be described below in detail with reference to examples. However, the present invention is not limited to these examples.

【0034】親水性被膜の性能評価は以下の方法により
評価した。 ■親水性評価:水の接触角測定で評価 (測定機器)協和界面科学製CA−A型 (測定環境)室温/大気中 (水滴量) 20μl [合否判定]水の接触角が5°以下であるものを合格と
した ■防曇性評価:水道水で一旦膜全体を水で濡らし水膜の
形成状態と水膜を維持する時間を評価した (測定環境)温度;20〜30℃、湿度;80〜90%
RH [合否判定]水膜形成状態 ;目視で水膜が均一に形成されているもの を合格とした 水膜維持時間 ;一旦水で表面を濡らして水膜を形成し、 水膜が形成されている時間が30分以上 であるものを合格とした ■映像評価:映像の鮮明さ、二重像の評価を目視で評価
した [合否判定]通常鏡と同様に見える場合を合格とした ■膜硬度評価:鉛筆硬度試験(JIS K5400) [合否判定]鉛筆硬度5H以上のものを合格とした ■耐酸試験 :25℃、1N塩酸に24時間浸漬した
後、流水下でガーゼ布で強く擦りキズおよび膜剥離の有
無を調べた [合否判定]キズおよび膜剥離がないものを合格とした ■耐アルカリ試験:25℃、1N水酸化ナトリウムに2
4時間浸漬した後、流水下でガーゼ布で強く擦りキズお
よび膜剥離の有無を調べた [合否判定]キズおよび膜剥離がないものを合格とし
た。
The performance of the hydrophilic coating was evaluated by the following method. ■ Hydrophilicity evaluation: Evaluated by measuring the contact angle of water (Measurement equipment) CA-A type manufactured by Kyowa Interface Science (Measurement environment) Room temperature / in the air (Water drop volume) 20 μl (1) The anti-fogging property was evaluated: the entire membrane was once wetted with tap water, and the state of formation of the water membrane and the time for maintaining the water membrane were evaluated (measurement environment): temperature; 80-90%
RH [Pass / fail judgment] Water film formation state: Visually, a water film was uniformly formed. Passed water film maintenance time; Wet the surface once with water to form a water film. ■ Evaluation of image clarity and double image was visually evaluated. [Pass / Fail] Judged as acceptable if it looks like a normal mirror. ■ Film hardness Evaluation: Pencil hardness test (JIS K5400) [Pass / Fail] Pencil hardness of 5H or more was accepted. ■ Acid resistance test: After immersion in 25 ° C and 1N hydrochloric acid for 24 hours, it was strongly rubbed with a gauze cloth under running water and scratches and film were observed. The presence or absence of peeling was checked. [Pass / Fail] Those without scratches and film peeling were accepted. ■ Alkali resistance test: 25 ° C, 2N in 1N sodium hydroxide
After immersion for 4 hours, it was strongly rubbed with a gauze cloth under running water, and the presence or absence of scratches and film peeling was examined.

【0035】なお、下記の実施例および比較例における
上記の性能評価結果を表1に示す。
Table 1 shows the results of the above performance evaluations in the following Examples and Comparative Examples.

【0036】[0036]

【実施例1】ゾル溶液の調製:出発原料として、マト
リックス形成用シリカゾル(リクソンコートCSG−D
I−0600、チッソ製)、テトライソプロピルチタネ
ートをアセチルアセトンでキレート化した自作の溶液、
超微粒子コロイダルシリカ(IPA−ST−S、日産化
学製)を用い、希釈溶媒には変性アルコール(エキネン
F−1)を用いた。溶液は以下の手順で調製した。
Example 1 Preparation of sol solution: As a starting material, a silica sol for matrix formation (Rixon coat CSG-D
I-0600, manufactured by Chisso), a self-made solution obtained by chelating tetraisopropyl titanate with acetylacetone,
Ultrafine particle colloidal silica (IPA-ST-S, manufactured by Nissan Chemical Industries, Ltd.) was used, and denatured alcohol (Ekinen F-1) was used as a diluting solvent. The solution was prepared according to the following procedure.

【0037】ゾル溶液組成は、酸化物換算でシリカ:チ
タニア:超微粒子シリカ=40:40:20重量%と
し、所定量のリクソンコートと自作のチタニアゾルおよ
びコロイダルシリカを、所定量のエキネンF−1が入っ
たビーカーに順次添加し室温で攪拌してコーティング溶
液とした。なお、溶液の固形分濃度は全酸化物換算で4
重量%とした。
The sol solution composition is silica: titania: ultrafine silica = 40: 40: 20% by weight in terms of oxide, and a predetermined amount of Rixon coat, a self-made titania sol and colloidal silica, and a predetermined amount of Echinen F-1 Were added sequentially to a beaker and stirred at room temperature to obtain a coating solution. The solid content of the solution was 4 in terms of total oxides.
% By weight.

【0038】コーティングおよび焼成:基板には10
cm□で厚さ5mmのフロートガラスを使用し、コーテ
ィング面を酸化セリウムで十分に研磨した後、ブラシ先
浄機で洗浄した後、イソプロピルアルコールでコーティ
ング面を払拭し基板とした。なお、裏面側は養生テープ
でマスキングした。このようにして準備したガラス基板
に上記溶液をディッピング法により、2mm/secの
速度でコーティングし、コーティング終了後に裏面側の
養生テープを剥がして、150℃なっている乾燥機で1
0分間乾燥して室温まで冷却後、550℃で30分間焼
成した。得られた膜は反射、透過とも色調はニュートラ
ルで、膜厚は触針式表面粗さ計(DEKTAK303
0、SLOAN社製)で測定した結果、200nmであ
った。膜表面の組織は図1に示すようなものでり、可視
光透過率は88%、曇価(ヘーズ)は5.7%であっ
た。なお、図1は、膜の表面形状の組織を示す顕微鏡写
真(400倍)である なお、親水性評価をした結果、被膜の水に対する接触角
は2〜3°と良好であるとともに、その他の性能評価結
果も表1に示す通りすべて良好であった。なお、防曇性
を評価するために、金属酸化物を形成している裏側に
は、スパッタリング法により膜厚が70nmの金属チタ
ンを成膜し、鏡面処理した。
Coating and firing: 10 for substrate
Using a float glass having a size of 5 cm and a thickness of 5 mm, the coated surface was sufficiently polished with cerium oxide, washed with a brush pre-cleaner, and then wiped with isopropyl alcohol to obtain a substrate. The back side was masked with a curing tape. The glass substrate prepared in this way was coated with the above solution at a rate of 2 mm / sec by a dipping method, and after the coating was completed, the curing tape on the back side was peeled off.
After drying for 0 minutes and cooling to room temperature, it was baked at 550 ° C. for 30 minutes. The resulting film has a neutral color tone for both reflection and transmission, and has a thickness of a stylus type surface roughness meter (DEKTAK303).
0, manufactured by SLOAN Co., Ltd.). The structure of the film surface was as shown in FIG. 1, and the visible light transmittance was 88% and the haze was 5.7%. In addition, FIG. 1 is a micrograph (400 times) showing the structure of the surface shape of the film. As a result of the hydrophilicity evaluation, the contact angle of the coating film with water was as good as 2 to 3 °, and other characteristics were obtained. The performance evaluation results were all good as shown in Table 1. In order to evaluate the anti-fogging property, a metal titanium film having a thickness of 70 nm was formed by sputtering on the back side on which the metal oxide was formed, and mirror-finished.

【0039】[0039]

【表1】 [Table 1]

【0040】[0040]

【実施例2】ゾル溶液組成をシリカ:チタニア:超微粒
子アルミナ=40:40:20重量%とした以外はすべ
て実施例1と同様で、焼成後の膜厚は180nmであっ
た。膜表面の組織は図1に示すようなものでり、可視光
透過率は87%、ヘーズは6.4%であった。なお、親
水性評価をした結果、被膜の水に対する接触角は1〜2
°と良好であるとともに、その他の性能評価結果も表1
に示す通りすべて良好であった。
Example 2 The same procedure as in Example 1 was conducted except that the sol solution composition was changed to silica: titania: ultrafine alumina = 40: 40: 20% by weight, and the film thickness after firing was 180 nm. The structure of the film surface was as shown in FIG. 1, and the visible light transmittance was 87% and the haze was 6.4%. As a result of the hydrophilicity evaluation, the contact angle of the coating film with water was 1-2.
°, and other performance evaluation results are shown in Table 1.
All were good as shown in FIG.

【0041】[0041]

【実施例3】ゾル溶液組成をシリカ:チタニア:超微粒
子シリカ:超微粒子アルミナ=40:40:10:10
重量%とした以外はすべて実施例1と同様で、焼成後の
膜厚は150nmであった。膜表面の組織は図1に示す
ようなものとなっており、可視光透過率は89%、ヘー
ズは11.8%であった。なお、親水性評価をした結
果、被膜の水に対する接触角は2〜3°で良好であると
ともに、性能評価結果も表1に示す通りすべて良好であ
った。
EXAMPLE 3 The sol solution composition was silica: titania: ultrafine silica: ultrafine alumina = 40: 40: 10: 10
All were the same as Example 1 except that the weight% was used, and the film thickness after firing was 150 nm. The structure of the film surface was as shown in FIG. 1, and the visible light transmittance was 89% and the haze was 11.8%. As a result of the hydrophilicity evaluation, the contact angle of the coating film with water was good at 2-3 °, and the performance evaluation results were all good as shown in Table 1.

【0042】[0042]

【実施例4】ゾル溶液組成をシリカ:チタニア:ジルコ
ニア:超微粒子シリカ=30:30:30:10重量%
とした以外はすべて実施例1と同様で、焼成後の膜厚は
220nmであった。膜表面の組織は図1に示すような
ものとなっており、可視光透過率は87%で、ヘーズは
12.3%であった。なお、親水性評価をした結果、被
膜の水に対する接触角は3〜4°で良好であるととも
に、性能評価結果も表1に示す通りすべて良好であっ
た。なお、ジルコニアの原料にはジルコニウム−n−ブ
トキシド(試薬、キシダ化学製)を用いた。
Example 4 The sol solution composition was silica: titania: zirconia: ultrafine silica = 30: 30: 30: 10% by weight.
Except for the above, all were the same as in Example 1, and the film thickness after firing was 220 nm. The structure of the film surface was as shown in FIG. 1, and the visible light transmittance was 87% and the haze was 12.3%. As a result of the hydrophilicity evaluation, the contact angle of the coating film with water was 3 to 4 °, which was good, and the performance evaluation results were all good as shown in Table 1. Note that zirconium-n-butoxide (reagent, manufactured by Kishida Chemical) was used as a raw material for zirconia.

【0043】[0043]

【比較例1】ゾル溶液組成を酸化物換算でシリカ:チタ
ニア:超微粒子シリカ=30:30:40重量%とした
以外はすべて実施例1と同様で、焼成後の膜厚は140
nmであった。膜表面の組織は図1に示すようなものと
なっており、可視光透過率は90%で、ヘーズは11.
1%であった。なお、性能評価をした結果、被膜の水に
対する初期接触角は2〜3°と良好であったが、鉛筆硬
度がH以下、耐アルカリ試験で膜が剥離し好ましいもの
ではなっかた。
Comparative Example 1 The same procedure as in Example 1 was carried out except that the sol solution composition was changed to silica: titania: ultrafine silica = 30: 30: 40% by weight in terms of oxide, and the film thickness after firing was 140.
nm. The structure of the film surface is as shown in FIG. 1, the visible light transmittance is 90%, and the haze is 11.
1%. As a result of the performance evaluation, the initial contact angle of the coating film with water was as good as 2 to 3 [deg.], But the pencil hardness was H or less and the film was peeled off in the alkali resistance test.

【0044】[0044]

【比較例2】ゾル溶液組成を酸化物換算でシリカ:チタ
ニア:超微粒子シリカ=45:45:5重量%とした以
外はすべて実施例1と同様で、焼成後の膜厚は160n
mであった。膜表面の組織は図1に示すようなものとは
なっておらず、フラット状の表面であった。可視光透過
率は82%で、ヘーズは0.7%であった。なお、性能
評価をした結果、被膜の水に対する初期接触角は8〜9
°と好ましいものではなく、また防曇性評価でも、一旦
水で濡らすことで均一な水膜は形成されたが、水膜を維
持できる時間が1分以内で好ましいものではなっかた。
Comparative Example 2 The same procedure as in Example 1 was carried out except that the sol solution composition was changed to silica: titania: ultrafine silica = 45: 45: 5% by weight in terms of oxide, and the film thickness after firing was 160 n.
m. The structure of the film surface was not as shown in FIG. 1 and was a flat surface. The visible light transmittance was 82% and the haze was 0.7%. As a result of the performance evaluation, the initial contact angle of the coating with water was 8 to 9
° is not preferable, and in the evaluation of the anti-fogging property, a uniform water film was formed by wetting once with water, but the time during which the water film could be maintained was not preferable within 1 minute.

【0045】[0045]

【比較例3】ゾル溶液組成を酸化物換算でシリカ:チタ
ニア:超微粒子シリカ=20:70:10重量%とした
以外はすべて実施例1と同様で、焼成後の膜厚は200
nmであった。膜表面の組織は図1に示すようなものと
なっており、可視光透過率は73%で、ヘーズは6.4
%であった。なお、性能評価をした結果、被膜の水に対
する初期接触角は2〜3°と好ましいものであったが、
膜面の反射率が高いために、像が二重に映り、鏡として
の機能を持ち合わせてはいなかった。
Comparative Example 3 The same procedure as in Example 1 was carried out except that the sol solution composition was changed to silica: titania: ultrafine silica = 20: 70: 10% by weight in terms of oxide, and the film thickness after firing was 200.
nm. The structure of the film surface is as shown in FIG. 1, the visible light transmittance is 73%, and the haze is 6.4.
%Met. In addition, as a result of performance evaluation, the initial contact angle of the coating film to water was preferably 2-3 °,
Due to the high reflectivity of the film surface, the image appeared double and did not have the function as a mirror.

【0046】[0046]

【比較例4】ガラス基板の片面をノングレアー処理(ガ
ラス表面をすりガラス調に処理)したガラス(ハリオ
製)で、グレアー度が#80で図1に示すような表面組
織を有するガラスをサンプルとした。可視光透過率は8
7%で、ヘーズは8.7%であった。性能評価結果は、
水に対する接触角は4〜5°と好ましいものであった
が、防曇性評価で、一旦水で濡らすことで均一な水膜は
形成されたが、水膜を維持できる時間が2分以内で好ま
しいものではなっかた。
Comparative Example 4 A glass (hario) having one surface of a glass substrate subjected to non-glare treatment (glass surface treated to a frosted glass) and having a glare degree of # 80 and having a surface structure as shown in FIG. 1 was used as a sample. . Visible light transmittance is 8
At 7%, the haze was 8.7%. The performance evaluation results
Although the contact angle with water was preferably 4-5 °, a uniform water film was formed by wetting once with water in the evaluation of antifogging property, but the time during which the water film could be maintained was within 2 minutes. It was not a good thing.

【0047】[0047]

【発明の効果】本発明の浴室用防曇鏡およびその製造方
法によれば、安定かつ確実に厄介な工程もなく手軽に容
易な特定の手段をもって、繰り返しの使用によっても優
れた防曇性を長時間に渡って維持できるとともに、金属
酸化物薄膜を安価にまた効率よく高生産性で得ることが
でき、クラック等の欠陥もなく、かつ鏡としての機能も
損なうことなく耐久性に優れ、耐摩耗性、耐薬品性にお
いても実用上問題のないものを提供することができる。
According to the antifogging mirror for bathrooms and the method of manufacturing the same of the present invention, excellent antifogging property can be obtained even by repeated use with a specific means which is stable, reliable and easy without any troublesome steps and easily. In addition to being able to be maintained for a long time, a metal oxide thin film can be obtained inexpensively and efficiently with high productivity, has no defects such as cracks, and has excellent durability without impairing the function as a mirror. A material having no practical problem in abrasion and chemical resistance can be provided.

【図面の簡単な説明】[Brief description of the drawings]

【図1】金属酸化物被膜の表面形状の組織を示す顕微鏡
写真(400倍)である。
FIG. 1 is a photomicrograph (× 400) showing the structure of the surface shape of a metal oxide film.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 西田 佳弘 三重県松阪市大口町1510 セントラル硝子 株式会社硝子研究所内 (72)発明者 本城 啓司 三重県松阪市大口町1510 セントラル硝子 株式会社硝子研究所内 Fターム(参考) 3B111 AA01 AC01 AC03 AD01 BC01 BC03 BD01 CA03 CC01 CD01 CE01 4G059 AA11 AC01 AC21 EA01 EA04 EA05 EA18 EB05  ──────────────────────────────────────────────────の Continuing on the front page (72) Inventor Yoshihiro Nishida 1510 Oguchi-cho, Matsusaka-shi, Mie Central Glass Laboratory Co., Ltd. (72) Inventor Keiji Honjo 1510 Oguchi-cho, Matsusaka-shi, Mie Central Glass Co., Ltd. F term (reference) 3B111 AA01 AC01 AC03 AD01 BC01 BC03 BD01 CA03 CC01 CD01 CE01 4G059 AA11 AC01 AC21 EA01 EA04 EA05 EA18 EB05

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】基板の片面に鏡面処理が施されている鏡の
反対側表面に、マトリックス形成用金属酸化物中に10
〜30重量%の吸水性超微粒子が均一に分散された表面
が凹凸形状を有する金属酸化物膜が被覆され、且つ該膜
の曇価が1%以上20%以下であることを特徴とする防
曇鏡。
1. A method according to claim 1, wherein one side of the substrate is mirror-finished and the other side of the mirror is covered with a metal oxide for matrix formation.
A metal oxide film having a surface with irregularities in which about 30% by weight of water-absorbing ultrafine particles are uniformly dispersed, and a haze value of the film is 1% or more and 20% or less. Cloudy mirror.
【請求項2】金属酸化物被膜が被覆された基板の可視光
線透過率は80%〜94%であることを特徴とする請求
項1記載の防曇鏡。
2. The anti-fog mirror according to claim 1, wherein the visible light transmittance of the substrate coated with the metal oxide film is 80% to 94%.
【請求項3】浴室用の紫外線なしで水に濡れた状態で防
曇性を持続し、二重像を形成しないことを特徴とする請
求項1乃至2記載の防曇鏡。
3. The anti-fog mirror according to claim 1, wherein the anti-fog mirror maintains the anti-fogging property in a state of being wetted by water without ultraviolet rays for a bathroom and does not form a double image.
【請求項4】吸水性微粒子、マトリックス形成用金属酸
化物用原料、および溶媒とを均一に混合し調整した溶液
を、基板の片側面に鏡面処理が施こされてなる鏡の反対
側表面に塗布した後、焼成して金属酸化物膜を固着させ
ることを特徴とする防曇鏡の製造方法。
4. A solution prepared by uniformly mixing and adjusting water-absorbing fine particles, a raw material for a matrix-forming metal oxide, and a solvent is applied to the opposite surface of a mirror having one surface of a substrate subjected to mirror finishing. A method for manufacturing an anti-fog mirror, comprising applying and firing to fix a metal oxide film.
JP11071234A 1999-03-17 1999-03-17 Antifogging mirror and its production Pending JP2000262367A (en)

Priority Applications (1)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11071234A JP2000262367A (en) 1999-03-17 1999-03-17 Antifogging mirror and its production

Publications (1)

Publication Number Publication Date
JP2000262367A true JP2000262367A (en) 2000-09-26

Family

ID=13454814

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2000262367A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1275624A1 (en) * 2001-06-29 2003-01-15 Crystal Systems Inc. Antifogging product, inorganic hydrophilic hard layer forming material and process for producing antifogging lens
EP1364924A1 (en) * 2002-05-13 2003-11-26 Schott Glas Decorating panel with metallic appearance and process for fabrication
JP2015110313A (en) * 2013-10-31 2015-06-18 セントラル硝子株式会社 Hydrophilic coating-formed article, hydrophilic coating-forming coat liquid and method for producing hydrophilic coating-formed article
JP2015110314A (en) * 2013-11-08 2015-06-18 セントラル硝子株式会社 Hydrophilic coating-formed article, hydrophilic coating-forming coat liquid and method for producing hydrophilic coating-formed article
JP2017185634A (en) * 2016-04-01 2017-10-12 岡本硝子株式会社 Antifogging article
WO2018202595A1 (en) * 2017-05-04 2018-11-08 Agc Glass Europe Coated substrate

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1275624A1 (en) * 2001-06-29 2003-01-15 Crystal Systems Inc. Antifogging product, inorganic hydrophilic hard layer forming material and process for producing antifogging lens
CN1302312C (en) * 2001-06-29 2007-02-28 株式会社水晶系统 Antifogging products, inorganic hydrophilic hard coating forming material and method for mfg. anti-fog lens
EP1364924A1 (en) * 2002-05-13 2003-11-26 Schott Glas Decorating panel with metallic appearance and process for fabrication
JP2015110313A (en) * 2013-10-31 2015-06-18 セントラル硝子株式会社 Hydrophilic coating-formed article, hydrophilic coating-forming coat liquid and method for producing hydrophilic coating-formed article
JP2015110314A (en) * 2013-11-08 2015-06-18 セントラル硝子株式会社 Hydrophilic coating-formed article, hydrophilic coating-forming coat liquid and method for producing hydrophilic coating-formed article
JP2017185634A (en) * 2016-04-01 2017-10-12 岡本硝子株式会社 Antifogging article
WO2018202595A1 (en) * 2017-05-04 2018-11-08 Agc Glass Europe Coated substrate
CN110621629A (en) * 2017-05-04 2019-12-27 旭硝子欧洲玻璃公司 Coated substrate
JP2020519553A (en) * 2017-05-04 2020-07-02 エージーシー グラス ユーロップAgc Glass Europe Coated substrate
US11008248B2 (en) 2017-05-04 2021-05-18 Agc Glass Europe Coated substrate
CN110621629B (en) * 2017-05-04 2022-07-29 旭硝子欧洲玻璃公司 Coated substrate
JP7149962B2 (en) 2017-05-04 2022-10-07 エージーシー グラス ユーロップ coated substrate

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