JP3385159B2 - Sol-gel film and method for forming the same - Google Patents
Sol-gel film and method for forming the sameInfo
- Publication number
- JP3385159B2 JP3385159B2 JP13387896A JP13387896A JP3385159B2 JP 3385159 B2 JP3385159 B2 JP 3385159B2 JP 13387896 A JP13387896 A JP 13387896A JP 13387896 A JP13387896 A JP 13387896A JP 3385159 B2 JP3385159 B2 JP 3385159B2
- Authority
- JP
- Japan
- Prior art keywords
- sol
- solution
- gel film
- film
- 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.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/22—Surface treatment of glass, not in the form of fibres or filaments, by coating with other inorganic material
- C03C17/23—Oxides
- C03C17/25—Oxides by deposition from the liquid phase
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL 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
- C03C2218/00—Methods for coating glass
- C03C2218/10—Deposition methods
- C03C2218/11—Deposition methods from solutions or suspensions
- C03C2218/113—Deposition methods from solutions or suspensions by sol-gel processes
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Surface Treatment Of Glass (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、凹凸状表層の形状
および大きさ等を適宜種々に安定してコントロールする
ことができ、かつ短く簡便な調合方法でもってより簡便
に得ることができる優れたコ─ティング溶液で表面形状
とその発現をより安定せしめてより比表面積を増大で
き、高硬度で機械的強度および耐久性が高い酸化物被膜
となる微細な凹凸状表層を有するゾルゲル膜及びその形
成法に関する。TECHNICAL FIELD The present invention is excellent in that the shape and size of the uneven surface layer can be appropriately and stably controlled in various ways and can be obtained more easily by a short and simple preparation method. A sol-gel film with a fine uneven surface layer that can stabilize the surface shape and its expression with a coating solution and increase the specific surface area, and becomes an oxide film with high hardness and high mechanical strength and durability, and its formation Concerning the law.
【0002】特にガラス基板上に被膜積層する多層膜に
おいて下地層膜として用いた際に、当該特異なゾルゲル
膜上に被覆する各種機能性膜の付着効率と密着性を高
め、しかも格段にその性能を発揮することとなる等、光
学特性を損なうことなく、長期的に頑固な密着力で耐摩
耗性あるいは耐久性等が優れたものとすることができ、
建築用もしくは自動車用等の窓材、船舶や航空機の窓材
などの各種膜付きガラス物品において有用なゾルゲル膜
およびその形成法を提供するものである。Particularly when used as an underlayer film in a multi-layer film laminated on a glass substrate, the adhesion efficiency and adhesion of various functional films coated on the peculiar sol-gel film are enhanced, and the performance is remarkably improved. It is possible to obtain excellent wear resistance or durability with long-term stubborn adhesion without impairing the optical characteristics such as exhibiting
The present invention provides a sol-gel film and a method for forming the sol-gel film, which are useful in window materials for construction or automobiles, glass materials for various films such as window materials for ships and aircraft.
【0003】[0003]
【従来の技術とその課題】一般に金属酸化物被膜の表面
に凹凸状を形成する方法としては、例えば金属酸化物被
膜をフッ酸やフッ硝酸等でエッチングする方法、あるい
は加熱処理により燃焼分解する有機高分子を金属アルコ
キシド溶液中に添加する方法等が知られている。また簡
単な工程で凹凸状等を形成する方法としては、本出願人
は出発原料の異なる金属アルコキシドを加水分解ならび
に脱水縮合させたゾル溶液を混合することによる方法を
見い出している。2. Description of the Related Art Generally, as a method for forming irregularities on the surface of a metal oxide coating, for example, a method of etching the metal oxide coating with hydrofluoric acid, hydrofluoric nitric acid, or the like, or an organic material which is decomposed by combustion by heat treatment, is used. A method of adding a polymer to a metal alkoxide solution is known. Further, as a method for forming irregularities and the like in a simple process, the present applicant has found a method by mixing a sol solution obtained by hydrolyzing and dehydrating and condensing metal alkoxides having different starting materials.
【0004】ところが金属酸化物被膜をフッ酸やフッ硝
酸等でエッチングする方法では、エッチング用溶液であ
るフッ酸やフッ硝酸等が人体に対し極端に危険な物質で
あってその取り扱いが厄介で作業性が劣るとともに、エ
ッチング工程を付加することでの生産性の低下等があ
り、また加熱処理により燃焼分解する有機高分子を金属
アルコキシド溶液中に添加する方法では、例えば一度形
成されたマイクロピット状表面が400 ℃以上の加熱焼成
により、被膜の緻密化が起こるため、その加熱処理条件
を種々制御する必要があるという制約があり、この制約
により頑固な被膜を得ることが困難であって、必ずしも
容易にとは言い難いものである。However, in the method of etching a metal oxide film with hydrofluoric acid, nitric acid, etc., the etching solution, hydrofluoric acid, hydrofluoric acid, etc., is an extremely dangerous substance to the human body, and its handling is troublesome. In addition to being poor in productivity, there is a decrease in productivity due to the addition of an etching step, and in the method of adding an organic polymer that is decomposed by combustion by heat treatment to a metal alkoxide solution, for example, micropits formed once There is a constraint that it is necessary to control the heat treatment conditions variously because the coating becomes dense by heating and baking the surface at 400 ° C or higher. Due to this constraint, it is difficult to obtain a stubborn coating, It is hard to say easily.
【0005】そこで、本出願人が既に出願している例え
ば特開平5-147976号公報に記載のマイクロピット状表層
を有する酸化物薄膜および該薄膜を用いた多層膜、なら
びにその形成法、また例えば特開平6-298545号公報に記
載のゾルゲル膜およびその形成法、さらに特開平7-1380
50号に記載の撥水性酸化物被膜およびその形成法等が上
記の点を解決するに際し有用であることを提案してい
る。Therefore, an oxide thin film having a micropit-like surface layer described in Japanese Patent Application Laid-Open No. 5-147976, a multilayer film using the thin film, and a method for forming the thin film, which have been already filed by the present applicant, for example, JP-A-6-298545, a sol-gel film described in JP-A-6-298545, and a method for forming the same, further JP-A-7-380
It has been proposed that the water-repellent oxide coating described in No. 50, its forming method, and the like are useful in solving the above problems.
【0006】自動車用窓ガラス等において各種機能性膜
が実用されるようになってきている最近では、調合方法
として調合温度や時間を増大させることなくより簡便で
長時間を要せず、またポットライフも優れたコ−ティン
グ溶液で、成膜環境として高湿度を必要とせず、表面形
状の発現がより安定かつより優れしかも長期間の過酷な
条件下でも機械的膜強度あるいは耐薬品性等耐久性に優
れるゾルゲル膜、特に下地層としてのゾルゲル膜がさら
にますます望まれつつある。Recently, various functional films have been put into practical use in window glass for automobiles, etc. In recent years, as a mixing method, it is simpler and does not take a long time without increasing the mixing temperature and time. It is a coating solution with an excellent life, does not require high humidity as a film forming environment, is more stable in surface shape development, and has excellent mechanical film strength or chemical resistance even under long-term harsh conditions. A sol-gel film having excellent properties, especially a sol-gel film as an underlayer, is being increasingly desired.
【0007】[0007]
【課題を解決するための手段】本発明は、従来のかかる
問題点に鑑みてなされたものであって、特定の金属アル
コキシドを添加したテトラアルコキシシランと、特定の
アルキルトリアルコキシシランとをそれぞれ加水分解な
らびに脱水縮合させたそれぞれのゾルゲル溶液を混合す
るとともに、特定の溶剤とジオ−ル類を混合して調製す
ることで性能が優れるコーティング溶液とし、ガラス基
板に該コーティング溶液を成膜して得られたゾルゲル膜
は高硬度かつ高密着性であって耐久性や耐摩耗性とを併
せ持ち、例えば独立してしっかりした特異な微細な凹凸
状表面表層を制御性よく極めて安定して発現し、より比
表面積の増大による被覆膜の付着効率と密着性の向上を
もたらし、格段に優れた下地層となり、しかも高安全で
厄介な工程なく、安価に効率よく機械的膜強度および耐
久性ならびに各種機能を発揮する酸化物薄膜を得ること
ができる有用なゾルゲル膜が形成できる塗布液およびゾ
ルゲル膜の形成法を提供するものである。DISCLOSURE OF THE INVENTION The present invention has been made in view of the above-mentioned problems in the prior art, and hydrolyzes a tetraalkoxysilane to which a specific metal alkoxide is added and a specific alkyltrialkoxysilane. A coating solution with excellent performance is prepared by mixing the decomposed and dehydrated condensed sol-gel solutions together with a specific solvent and diols, and the coating solution is formed on a glass substrate to obtain a coating solution. The obtained sol-gel film has high hardness and high adhesiveness, and has durability and wear resistance, and, for example, independently and firmly expresses a unique fine uneven surface layer with excellent controllability and extremely stable expression. By increasing the specific surface area, the coating efficiency and adhesion of the coating film are improved, resulting in a significantly superior underlayer, and it is highly safe and has no troublesome process. There is provided valence formation method of efficiently mechanical film strength and durability as well as the coating solution and gel film useful sol-gel film can be formed which can be obtained oxide thin film that exhibits various functions.
【0008】すなわち、本発明は、ガラス基板の表面上
に、アセチルアセトンで安定化した金属アルコキシドを
添加したテトラアルコキシシランを加水分解ならびに脱
水縮合させたゾル溶液Aと、1つの官能基をアルキル基
化したアルキルトリアルコキシシランを加水分解ならび
に脱水縮合したゾル溶液Bとを混合した混合物と、イソ
プロピルアルコ−ルを主成分とする溶媒と、添加量が、
コ−ティング溶液中の全ての金属アルコキシドの合計固
形分に対し、0.5 〜30wt%であるジオ−ル類
と、からなるコ−ティング溶液を被覆し、加熱焼成する
ことで得る微細な凹凸状表層を有する酸化物薄膜で成る
ことを特徴とするゾルゲル膜。That is, according to the present invention, a sol solution A obtained by hydrolyzing and dehydrating and condensing a tetraalkoxysilane to which a metal alkoxide stabilized with acetylacetone is added, and one functional group is converted into an alkyl group on the surface of a glass substrate. A mixture of a sol solution B obtained by hydrolyzing and dehydrating and condensing the alkyltrialkoxysilane, a solvent containing isopropyl alcohol as a main component, and an addition amount of
The total solid content of all metal alkoxides in the coating solution.
It is characterized by comprising an oxide thin film having a fine uneven surface layer obtained by coating a coating solution consisting of 0.5 to 30 wt% of diols with respect to the shape and heating and baking. And a sol-gel film.
【0009】前記ゾルゲル膜の微細な凹凸状表層表面に
おける平均面粗さRa'値が、2.5〜15.8nmであ
ることを特徴とする前述のゾルゲル膜。 On the surface of the fine rugged surface layer of the sol-gel film
The average surface roughness Ra 'value in the range from 2.5 to 15.8 nm
The aforementioned sol-gel film, which is characterized in that
【0010】前記ゾルゲル膜を機能性多層膜の下地層と
して用いる。 The sol-gel film is used as an underlayer of the functional multilayer film.
To use.
【0011】又、前記ゾルゲル膜を撥水性ガラスの下地
層として用いる。 Further , the sol-gel film is coated with a water-repellent glass substrate.
Used as a layer.
【0012】さらには、前記ゾルゲル膜を低反射膜とし
て用いる。 Further, the sol-gel film is a low reflection film.
To use.
【0013】ガラス基板の表面上に、アセチルアセトン
で安定化した金属アルコキシドを添加したテトラアルコ
キシシランを加水分解ならびに脱水縮合させたゾル溶液
Aと、1つの官能基をアルキル基化したアルキルトリア
ルコキシシランを加水分解ならびに脱水縮合したゾル溶
液Bとを混合し、ジオール類の添加量が、コ−ティング
溶液中の金属アルコキシドの固形分に対し、0.5 〜
30wt%になるようにジオ−ル類を添加したアルコ─
ル系溶媒で適度の希釈をし、10℃乃至50℃の保持温
度で1乃至24時間攪拌した混合物を作製し、該混合物
をイソプロピルアルコ−ルを主成分とする溶媒で希釈し
調製してなるコ−ティング溶液を被膜し、乾燥加熱焼成
し微細な凹凸状表層を有する酸化物薄膜で成るようにす
ることを特徴とするゾルゲル膜の形成法。On the surface of a glass substrate, a sol solution A obtained by hydrolyzing and dehydrating and condensing a tetraalkoxysilane to which a metal alkoxide stabilized with acetylacetone is added, and an alkyltrialkoxysilane having one functional group alkylated. The sol solution B that has been hydrolyzed and dehydrated and condensed is mixed, and the amount of diols added is changed to the coating amount.
0.5 to the solid content of the metal alkoxide in the solution
Alcohol with diols added to 30 wt%
It is prepared by appropriately diluting with a solvent of a solvent and stirring the mixture at a holding temperature of 10 ° C to 50 ° C for 1 to 24 hours, and diluting the mixture with a solvent containing isopropyl alcohol as a main component. A method for forming a sol-gel film, which comprises coating a coating solution, drying and heating to form an oxide thin film having a fine uneven surface layer.
【0014】又、前記コ−ティング溶液における固形分
濃度が、酸化物換算で0.2〜5.0wt%になるよう
希釈調製することを特徴とする上述したゾルゲル膜の形
成法。 Also, the solid content in the coating solution
The concentration should be 0.2 to 5.0 wt% in terms of oxide.
Shape of the sol-gel film described above characterized by being prepared by dilution
Law.
【0015】[0015]
【0016】[0016]
【0017】[0017]
【0018】またさらに、前記コ−ティング溶液の粘度
を、1〜10cPに粘度調製することでなるコーテイング溶
液とすることを特徴とする上述したゾルゲル膜の形成法
をそれぞれ提供するものである。Furthermore, the above-mentioned methods for forming a sol-gel film are provided, wherein the coating solution is a coating solution prepared by adjusting the viscosity of the coating solution to 1 to 10 cP.
【0019】[0019]
【発明の実施の形態】ここで、前記したように、アセチ
ルアセトンで安定化した金属アルコキシドを添加したテ
トラアルコキシシランを加水分解ならびに脱水縮合させ
たゾル溶液Aと、1つの官能基がアルキル基化したアル
キルトリアルコキシシランを加水分解ならびに脱水縮合
したゾル溶液Bとを混合した混合物を用いることとした
のは、容易に溶液調製することができかつポットライフ
を長くでき、成膜した前記微細な凹凸状表層の表面形状
を有するものとなり、かつ機械的膜強度、耐薬品性に優
れ、酸化物薄膜の透明性や硬度が高く、耐久性にも優れ
たものとなり、比較的安価で入手し易いものであるので
該二つのゾル溶液を用いることとした。BEST MODE FOR CARRYING OUT THE INVENTION Here, as described above, a sol solution A obtained by hydrolyzing and dehydrating and condensing a tetraalkoxysilane to which a metal alkoxide stabilized with acetylacetone is added, and one functional group is converted into an alkyl group. The reason why the mixture of the sol solution B obtained by hydrolyzing and dehydrating and condensing the alkyltrialkoxysilane is used is that the solution can be easily prepared, the pot life can be lengthened, and the fine irregularities formed as a film can be formed. It has a surface morphology of the surface layer, has excellent mechanical film strength and chemical resistance, and has high transparency and hardness of the oxide thin film, and also has excellent durability, which is relatively inexpensive and easily available. Therefore, it was decided to use the two sol solutions.
【0020】また、二つのゾル溶液の一つが、アセチル
アセトンで安定化した金属アルコキシドを添加したテト
ラアルコキシシランである金属アルコキシド系化合物を
用い、加水分解ならびに脱水縮合したゾル溶液Aと、ゾ
ル溶液のもう一つが1つの官能基をアルキル基化したア
ルキルトリアルコキシシランである金属アルコキシド系
化合物を用い、加水分解ならびに脱水縮合したゾル溶液
Bとしたのは、ゾル溶液Aでは例えばーSiーO ーSiー
(但し、Siの上下方向の線は省略する)三次元構造が発
達しやすいものと該骨格が生成しにくいものを共存させ
る。一方、ゾル溶液Bでは、加水分解および脱水縮合反
応が起こらないアルキル基が存在するため、三次元構造
のSiーO ーSi結合等の骨格が生成しにくい。よってゾル
溶液Aとゾル溶液Bとを混合することにより被膜した際
に種々の表層が発現するようになり、数%程度の異種金
属元素が加わることにより、同一金属元素からなる薄膜
を緻密化させる働きが生じ、機械的膜強度および耐薬品
性等耐久性に優れる、しかも制御されかつ再現性よく安
定した形状と性能の微細な凹凸状表層薄膜となる。Further, one of the two sol solutions is a metal alkoxide compound which is a tetraalkoxysilane to which a metal alkoxide stabilized with acetylacetone is added. A sol solution B prepared by hydrolysis and dehydration condensation using a metal alkoxide compound, one of which is an alkyltrialkoxysilane in which one functional group is an alkyl group, is prepared in the sol solution A, for example, —Si—O—Si— (However, the lines in the vertical direction of Si are omitted.) Coexistence of a material in which a three-dimensional structure is easily developed and a material in which the skeleton is difficult to form. On the other hand, in the sol solution B, since an alkyl group that does not cause hydrolysis and dehydration condensation reaction is present, a skeleton such as a Si—O—Si bond having a three-dimensional structure is less likely to be generated. Therefore, when the sol solution A and the sol solution B are mixed, various surface layers are developed and a thin film made of the same metal element is densified by adding several% of different metal elements. A fine concavo-convex surface layer thin film having a function and excellent durability such as mechanical film strength and chemical resistance, and having a stable shape and performance which is controlled and reproducible.
【0021】さらに前記金属としては、格別特定するも
のではないが、Ti、AlまたはZrを選択するのが好まし
く、具体的なものとしては、例えばチタンテトラノルマ
ルブトキシド〔Ti(O-n-Bu)4 Bu:C4H9 〕、アルミニウム
トリノルマルブトキシド〔Al(0-n-Bu)3 〕、ジルコニウ
ムテトラノルマルブトキシド〔Zr(O-n-Bu)4 〕、または
Ti、Al、Zrのアセチルアセトネ−ト塩等が好適である。Further, although the metal is not particularly specified, it is preferable to select Ti, Al or Zr. Specific examples thereof include titanium tetranormal butoxide [Ti (On-Bu) 4 Bu. : C 4 H 9 ], aluminum trinormal butoxide [Al (0-n-Bu) 3 ], zirconium tetranormal butoxide [Zr (On-Bu) 4 ], or
Acetylacetonate salts of Ti, Al and Zr are suitable.
【0022】またさらに、前記1つの官能基をアルキル
基化したアルキルトリアルコキシシランとしては、具体
的には例えば、メチルトリエトキシシラン〔MeSi(OE
t)3〕、メチルトリメトキシシラン〔MeSi(OMe)3〕等が
好適である。Further, as the alkyltrialkoxysilane in which the one functional group is alkylated, specifically, for example, methyltriethoxysilane [MeSi (OE
t) 3 ], methyltrimethoxysilane [MeSi (OMe) 3 ] and the like are preferable.
【0023】また、微細な凹凸状表層における形状なら
びにその制御については、先ず前記ゾル溶液Aおよびゾ
ル溶液Bの官能基ならびに分子量であり、特に前記した
ような現象を発現する異種官能基、ことに4と3の官能
基のものが主であり、また例えば分子量としてはその範
囲が100 〜100,000 であり、100 未満では原料の加水分
解が不充分なため被膜時に膜ハジキが生じやすく、成膜
性が悪く、また100,000 を超えるとゾル溶液がゲル化を
生じ、ゾル溶液の安定性が悪くなる。好ましくは1,000
〜50,000程度のものがよい。Regarding the shape of the fine uneven surface layer and its control, firstly, the functional groups and molecular weights of the sol solutions A and B, especially the different functional groups that exhibit the above-mentioned phenomenon, The functional groups of 4 and 3 are mainly used, and the molecular weight is, for example, in the range of 100 to 100,000. If it is less than 100, hydrolysis of the raw material is insufficient and film cissing is likely to occur during film formation. When it exceeds 100,000, the sol solution gels and the stability of the sol solution deteriorates. Preferably 1,000
~ 50,000 is recommended.
【0024】もしくはならびに前記ゾル溶液を調製する
際の溶剤の種類であり、イソプロピルアルコ−ル、ブタ
ノ−ル、エタノ−ルのアルコ−ル溶媒、アセチルアセト
ン等であり、ことにイソプロピルアルコールを主成分と
してなるアルコールであって、なかでもコ−ティング溶
液の調製における希釈溶媒としては、イソプロピルアル
コールにブタノ−ルを約10wt%添加した希釈溶媒がよ
く、得られる薄膜の微細な凹凸状表層の表面形状の発現
の安定性に役立つこととなる。Alternatively, the type of the solvent used for preparing the sol solution is isopropyl alcohol, butanol, alcohol solvent of ethanol, acetylacetone, etc. Alcohol which is, among others, as the diluting solvent in the preparation of the coating solution, a diluting solvent in which butanol is added to isopropyl alcohol in an amount of about 10 wt% is preferable, and the diluting solvent of the surface profile of the fine uneven surface layer of the obtained thin film is obtained. It will help the stability of expression.
【0025】もしくはならびにゾル溶液における酸化物
換算での固形分の混合比であり、例えばゾル溶液Aの固
形分1gに対してゾル溶液Bの固形分は2〜6g程度で
あり、2g未満では得られた薄膜の表層が平坦状にな
り、また6gを超えると得られる薄膜の表層は粗大化す
ることとなり、所期のめざすものとはならない。好まし
くはゾル溶液Aの固形分1gに対してゾル溶液Bの固形
分は2.5 〜5.5 g程度である。Alternatively, it is the mixing ratio of the solid content of the sol solution in terms of oxide. For example, the solid content of the sol solution B is about 2 to 6 g with respect to 1 g of the solid content of the sol solution A. The surface layer of the obtained thin film becomes flat, and when it exceeds 6 g, the surface layer of the obtained thin film becomes coarse, which is not what is expected. Preferably, the solid content of the sol solution B is about 2.5 to 5.5 g per 1 g of the solid content of the sol solution A.
【0026】また、前記添加するジオ−ル類〔一般式:R
(OH)2 、DO類という。〕としては、例えば一般式:Cn H
2n (OH)2 (n≧2)であるエチレングリコ−ル(メチ
レン基:2)、1,3-プロパンDO、1,2-プロパンDO(以上、
メチレン基:3)、1,4-ブタンDO(1,4-BDO )、1,3-BDO
、1,2-BDO (以上、メチレン基:4)、1,5-ペンタンD
O、1,4-ペンタンDO、1,3-ペンタンDO、1,2-ペンタンDO
(以上、メチレン基:5)、1,6-ヘキサンDO(メチレン
基:6)、プロピレングリコ−ル、1,8-オクタンDO、1,9-
ノナンDO等の直鎖ジオ−ルまたは鎖状ジオ−ルが挙げら
れ、またさらに例えば一般式:Cn H2n-2(OH)2(n≧3)
であるシクロペンタン-1,2-DO 、シクロヘキサン-1,2-D
O 、シクロヘキサン-1,4-DO 等の環式ジオ−ルが挙げら
れる。Further, the dioles added [the general formula: R
(OH) 2 , called DO. ], For example, the general formula: C n H
2n (OH) 2 (n ≧ 2) ethylene glycol (methylene group: 2), 1,3-propane DO, 1,2-propane DO (above,
Methylene group: 3), 1,4-butane DO (1,4-BDO), 1,3-BDO
, 1,2-BDO (above, methylene group: 4), 1,5-pentane D
O, 1,4-pentane DO, 1,3-pentane DO, 1,2-pentane DO
(Above, methylene group: 5), 1,6-hexane DO (methylene group: 6), propylene glycol, 1,8-octane DO, 1,9-
Examples thereof include straight chain diols and chain diols such as nonane DO. Further, for example, the general formula: C n H 2n-2 (OH) 2 (n ≧ 3)
Cyclopentane-1,2-DO, cyclohexane-1,2-D
Examples thereof include cyclic diols such as O 2 and cyclohexane-1,4-DO.
【0027】またさらに、前記ジオ−ル類の添加量が、
コ−ティング溶液中の全ての金属アルコキシドの合計固
形分に対し、0.5 〜30wt%になるように調製することと
したのは、添加量が0.5 wt%未満では例えば比表面積を
増大する作用を抑制するようなこととなり、また30wt%
を超えるような添加をしたとしても、その添加量のわり
に比表面積を増大する作用効果等が得られず経済的でな
く、むしろ例えば膜の緻密性が最高な状態から多少下が
り、機械的膜強度などが低下するような傾向を発現する
等が見られるためである。好ましい前記ジオ−ル類の添
加量としては1〜20wt%程度、より好ましくは2〜15wt
%程度である。Furthermore, the addition amount of the diols is
With respect to the total solid content of all the metal alkoxides in the coating solution, 0.5 to 30 wt% was prepared so that when the addition amount is less than 0.5 wt%, for example, the effect of increasing the specific surface area is suppressed. And it will be 30 wt%
Even if the amount of addition exceeds the above, it is not economical because the effect of increasing the specific surface area is not obtained instead of the amount added, but rather, for example, the denseness of the film falls from the highest state to some extent, and the mechanical film strength increases. This is because, for example, a tendency to decrease such as is exhibited. The addition amount of the above-mentioned dioles is preferably about 1 to 20 wt%, more preferably 2 to 15 wt%.
%.
【0028】さらに、被膜する際の環境については、前
記ジオ−ル類の添加によってコ−ティング溶液の安定性
が増し、より確実に制御されかつ極めて再現性よくより
安定した形状と性能の微細な凹凸状表層薄膜をうること
ができ、原則的に格別限定する必要がなくなるものの、
温度と相対湿度を室温で例えば45〜70%程度にコントロ
ールすることによって、種々の表層形状ならびにその径
などをより再現性よく安定かつ確実に制御し得ることも
ある。Further, regarding the environment for coating, the stability of the coating solution is increased by the addition of the above-mentioned diols, and the coating solution is controlled more reliably and has extremely reproducible and stable shape and performance. Although it is possible to obtain an uneven surface thin film, it is not necessary to limit it in principle, but
By controlling the temperature and the relative humidity at room temperature to, for example, about 45 to 70%, various surface layer shapes and their diameters may be more reproducibly and stably and reliably controlled.
【0029】さらに、前記コーテイング溶液の粘度を1
〜10cPに調製するのは、1cP未満では粘性が低すぎて膜
となり難く、また10cPを超えると被膜した際に過剰に塗
膜され加熱乾燥過程で膜中にクラツク等が生じてしまう
ためである。Further, the viscosity of the coating solution is 1
The reason for adjusting to 10 cP is that if it is less than 1 cP, the viscosity is too low to form a film, and if it exceeds 10 cP, the film is excessively coated when coated and cracks and the like occur in the film during the heating and drying process. .
【0030】またさらに、前記コーテイング溶液の酸化
物換算固形分濃度を0.2 〜5.0 wt%としたのは、0.2 wt
%未満では希薄すぎるため膜の形態となり難く、また5.
0 wt%を超えると濃度が高すぎるため膜厚が厚くなり、
膜中にクラツクの発生を生じたりあるいは成膜時に白濁
を生じたりして良質な薄膜が得られないこととなるもの
である。Further, the solid content concentration of oxide of the coating solution is set to 0.2 to 5.0 wt% because it is 0.2 wt.
If it is less than%, it is too thin and it is difficult to form a film.
If it exceeds 0 wt%, the concentration will be too high and the film thickness will increase.
A crack is generated in the film, or white turbidity is generated during the film formation, so that a high quality thin film cannot be obtained.
【0031】さらにまた、ガラス基板への膜付け法とし
ては、ハケ塗り等の手動塗り、ノズルフロ−コ−ト法、
ディッピング法、スプレー法、フローコート法あるいは
スピンコート法、ならびにそれらの併用等既知の塗布
法、もしくは本出願人が出願提案した特異な塗布法など
種々の塗布手段が適宜採用し得るものである。Further, as a method for applying a film to a glass substrate, manual application such as brush application, nozzle flow coating method,
Various coating means such as a dipping method, a spray method, a flow coating method or a spin coating method, a known coating method such as a combination thereof, or a unique coating method proposed by the applicant of the present invention can be appropriately adopted.
【0032】また前記下地層であるゾルゲル膜の成膜す
る際における風乾等の乾燥後の加熱温度については、10
0 ℃以上700 ℃以下程度、好ましくは約500 ℃程度以上
670℃以下程度、さらに薄膜をより強固にするため、例
えば600 ℃程度あるいは以上の温度による焼成であっ
て、具体的にはガラス板の曲げあるいは/および強化工
程における温度であり、該温度でも消失することもな
く、種々の前記表面形状表層とすることができるもので
ある。Regarding the heating temperature after drying such as air drying when forming the sol-gel film as the underlayer,
0 ℃ or more and 700 ℃ or less, preferably about 500 ℃ or more
In order to make the thin film stronger at about 670 ° C or lower, for example, baking at a temperature of about 600 ° C or higher, specifically, the temperature in the bending or / and strengthening step of the glass plate, which disappears even at that temperature. Without doing so, various surface shape surface layers can be formed.
【0033】さらにまた、前記ガラス基板としては、フ
ロ−トガラス等各種無機質の透明板ガラスであって、無
色または着色、ならびにその種類あるいは色調、形状等
に特に限定されるものではなく、さらに曲げ板ガラスと
してはもちろん、各種強化ガラスや強度アップガラス、
平板や単板で使用できるとともに、複層ガラスあるいは
合せガラスとしても使用できることは言うまでもない。Further, the glass substrate is a transparent plate glass of various inorganic materials such as float glass, and is not particularly limited to colorless or colored, and its kind, color tone, shape, etc., and further as a bent plate glass. Of course, various tempered glass and strength up glass,
It goes without saying that it can be used as a flat plate or a single plate, and can also be used as a multilayer glass or a laminated glass.
【0034】前述したとおり、本発明の微細な凹凸状表
層を有するゾルゲル膜ならびにその形成法により、上述
したアセチルアセトンで安定化した金属アルコキシドを
添加したテトラアルコキシシランである4官能を有する
ものと、1つの官能基をアルキル基化したアルキルトリ
アルコキシシランである3官能を有するものとの二つの
特定系化合物を加水分解ならびに脱水縮合した2種類の
ゾル溶液を、特定の希釈溶媒で希釈し、特定量のジオ−
ル類を添加して特定選択し組み合わせて調製し用いるこ
とによってコーテイング溶液を得、さらに高いRa' 値を
得るのに比較的低い湿度環境で成膜することができ、そ
れに伴ってハジキや白濁等の現象もなくなり、コーティ
ング溶液として簡便に調合調製ができしかも格段に優れ
た安定性とその性能を有するものとでき、被膜で特異な
挙動を発現せしめて特異な形状構造をもたらし、加熱乾
燥または焼成および高温焼成等を行うことにより、緻密
化して平坦化することなく、従来より独立性等があって
深見のある、極めて明確でしっかりし安定した微細な凹
凸状表層となり、かつ膜強度のより高い酸化物薄膜とな
り、しかもより増大した比表面積を有する表面表層を格
段に安定かつ確実に制御でき、付着性も向上し強固な薄
膜とすることができ、ガラス基板との界面はもちろん、
多層膜での被覆膜との膜と膜の界面においても密着性を
格段に向上せしめ、被覆含浸した撥水性薄膜等機能性薄
膜を含め優れた機械的強度、耐候性、耐久性を有するも
のとなり、従来より格段に長期的に及ぶ優れた耐久性を
有するものとなり、透明で硬度が高い、しかも光学特性
等も充分に満足できるものとでき、屋外でも使用できる
ことはもちろんであり、高安全で厄介な工程なく、安価
に効率よく得られることとなるものであり、ことに建築
用はもちろん、船舶、航空機、自動車用等の車輌用の窓
材に採用して格段に有用となる。As described above, according to the sol-gel film having the fine uneven surface layer of the present invention and the method for forming the sol-gel film, the tetraalkoxysilane which is a tetraalkoxysilane to which the metal alkoxide stabilized with acetylacetone is added, and 1 Two specific sol solutions obtained by hydrolyzing and dehydrating two specific compounds, one having an alkyltrialkoxysilane having three functional groups, which is an alkyl group having one functional group as an alkyl group, are diluted with a specific diluent solvent to obtain a specific amount. Geo-
A coating solution can be obtained by adding and selecting specific substances to prepare a coating solution, and a film can be formed in a relatively low humidity environment to obtain a higher Ra 'value, which causes cissing and cloudiness. Can be easily prepared and prepared as a coating solution, and can have markedly superior stability and its performance. By expressing a unique behavior in the coating, a unique shape and structure can be obtained, and it can be dried by heating or baking. By performing high-temperature baking and the like, it becomes a finely defined, firm and stable fine uneven surface layer that is independent and deeper than before and does not become dense and flat, and has higher film strength. It becomes an oxide thin film, and the surface layer with a larger specific surface area can be controlled significantly more reliably and reliably, and the adhesion can be improved to form a strong thin film. , Not to mention the interface with the glass substrate,
It has excellent mechanical strength, weather resistance, and durability, including functional thin films such as water-repellent thin films that have been impregnated by coating, by significantly improving the adhesion at the interface between the coating film and the film in a multilayer film. Since it has excellent durability over a long period of time compared to the past, it is transparent and has high hardness, and its optical characteristics can be sufficiently satisfied. Of course, it can be used outdoors and is highly safe. It can be obtained efficiently at low cost without any troublesome process, and is particularly useful as a window material for vehicles such as ships, aircrafts and automobiles as well as construction.
【0035】[0035]
【実施例】以下、実施例により本発明を具体的に説明す
る。ただし本発明は係る実施例に限定されるものではな
い。EXAMPLES The present invention will be specifically described below with reference to examples. However, the present invention is not limited to the embodiment.
【0036】実施例1
大きさ約900mm x600mm 、厚さ約3.5 mmのクリア・フロ
−トガラス基板を中性洗剤、水すすぎ、アルコ−ルで順
次洗浄し、乾燥した後、アセトンで払拭し被膜用ガラス
基板とした。 Example 1 A clear float glass substrate having a size of about 900 mm x 600 mm and a thickness of about 3.5 mm was sequentially washed with a neutral detergent, a water rinse, an alcohol, dried and then wiped with acetone to form a film. A glass substrate was used.
【0037】テトラエトキシシラン(Si(OC2H5)4 :TE
0S)の重合ゾル(平均分子量 Mv=約2000〜3000)とアセ
チルアセトンで安定化したテトラブトキシチタン(Ti(O
-Bu) 4 )との混合ゾル(アセチルアセトンで安定化した
テトラブトキシチタンの含有量は酸化物換算でSiO2に対
して約0.25wt%、モル比で約 20mol%である)を、イソ
プロピルアルコ−ル(iPA )、ブタノ−ル、エタノ−ル
のアルコ−ル溶媒を加え、固形分濃度として酸化物換算
で約5wt%になるまで希釈したものをゾル溶液Aとし
た。〔例えば、大八化学工業(株)製、CG19-Ti-1 〕
メチルトリメトキシシラン(CH3Si(OCH3)3:MTMS)の重
合ゾル(平均分子量 Mv=約1,000 )にイソプロピルアル
コ−ル(iPA )を加え、固形分濃度として酸化物換算で
約20wt%になるまで希釈したものをゾル溶液Bとした。
〔例えば、大八化学工業(株)製、MTS-2 〕
上記ゾル溶液A20gとゾル溶液B20gと、加水分解およ
び脱水縮合反応の反応速度を調整し、かつコ−ティング
溶液中の分相をし易くなるため、1,3-ブタンジオ−ル
(以下、1,3-BDO という。) 0.4wt%含有せしめ修飾し
た調合用ブタノ−ル(以下、調合用BuOHという。BuOH50
g 中に1,3-BDO を0.2g含有したもの、水分量200ppm、な
お水分量は例えば0〜3500ppm の範囲であればよい)約
50gを約50℃で約3 時間密栓状態で混合攪拌し、さらに
90wt%iPA /10wt%BuOHの混合系溶媒で希釈してコ−テ
イング溶液を得た。この際の固形分濃度は酸化物換算で
約1.0 〜 1.2wt%程度であった。また1,3-BDO の添加量
としては、コ−ティング溶液中の全ての金属アルコキシ
ドの合計固形分に対し4wt%である。Tetraethoxysilane (Si (OC2HFive)Four: TE
0S) polymerized sol (average molecular weight Mv = approximately 2000-3000)
Tetrabutoxytitanium (Ti (O
-Bu) Four ) Mixed sol (stabilized with acetylacetone)
The content of tetrabutoxy titanium is SiO in terms of oxide.2Against
Is about 0.25 wt% and the molar ratio is about 20 mol%).
Propyl alcohol (iPA), butanol, ethanol
Alcohol solvent is added to convert the solid content to oxide.
Sol solution A diluted to approximately 5 wt%
It was [For example, CG19-Ti-1 manufactured by Daihachi Chemical Industry Co., Ltd.]
Methyltrimethoxysilane (CH3Si (OCH3)3: MTMS)
Combined sol (average molecular weight Mv = about 1,000) with isopropyl alcohol
Call (iPA) was added, and the solid content concentration was converted to oxide.
The sol solution B was diluted to about 20 wt%.
[For example, MTS-2 manufactured by Daihachi Chemical Industry Co., Ltd.]
20 g of the above sol solution A and 20 g of sol solution B
And control the reaction rate of dehydration condensation reaction and coating
1,3-butanediol was added to facilitate phase separation in the solution.
(Hereinafter, referred to as 1,3-BDO.) 0.4 wt% contained and modified
Butanol for blending (hereinafter referred to as BuOH for blending.
g containing 0.2 g of 1,3-BDO, water content of 200 ppm,
The water content may be in the range of 0-3500ppm)
Mix and stir 50g at about 50 ℃ for about 3 hours in a tightly closed state.
Dilute with a mixed solvent of 90wt% iPA / 10wt% BuOH to coat
An ingot solution was obtained. The solid content concentration at this time is calculated as oxide.
It was about 1.0 to 1.2 wt%. Also, the amount of 1,3-BDO added
As all metal alkoxy in the coating solution
It is 4 wt% with respect to the total solid content of the glass.
【0038】上述したのと同様にして、1,3-BDO の添加
量を、重量%で0%、2.5 %、5%、7.5 %、10%、15
%、20%、30%と0〜30wt%の範囲内で変えて調製し、
それぞれコ−テイング溶液を得た。In the same manner as described above, the amount of 1,3-BDO added was 0%, 2.5%, 5%, 7.5%, 10%, 15% by weight.
%, 20%, 30% and 0 to 30 wt% in the range of different preparation,
A coating solution was obtained in each case.
【0039】なお上述したなかで、ゾル溶液Aとゾル溶
液Bとの比は固形分の重量比で約1:4程度、より好ま
しい当該比は約1:3.5 〜5.5 程度である。またなお混
合後の攪拌時間は、例えば好ましい当該攪拌時間は約50
℃の温度であれば1〜6時間(蜜栓)程度乃至約25℃の
温度であれば3〜6時間(蜜栓)程度である。またな
お、該溶液を短期間で使用する際あるいは膜のグレ‐ド
等によっては、微細な経時変化を考慮する必要がなく、
室温で攪拌をしないでもよい場合もある。In the above description, the ratio of the sol solution A to the sol solution B is about 1: 4 by weight of the solid content, and the more preferred ratio is about 1: 3.5 to 5.5. The stirring time after mixing is, for example, preferably about 50.
If the temperature is ℃, it is about 1 to 6 hours (honey stopper) to about 25 ° C., it is about 3 to 6 hours (honey stopper). Furthermore, when the solution is used in a short period of time or depending on the grade of the film, it is not necessary to consider a minute change with time,
In some cases, stirring may not be necessary at room temperature.
【0040】次いで、スピン成膜条件として、スピンコ
−タ−上にガラス基板をセットし、先ずスピン回転を開
始後1〜3秒で回転速度が約150rpm(例えば約50〜250r
pm程度、高速スピン回転)し、上記した各コーテイング
溶液(塗布液)を約100ml 程度滴下し、約19〜17秒程度
回転速度を維持し被膜した。次にで被膜化した塗布液が
渇きはじめて流動性を失うようになる前に、スピン回転
を一旦停止し約60秒間程度静止してレベリングせしめ、
再度スピン回転を始め、約50rpm 程度(例えば約20〜10
0rpm程度)の低速回転で約40秒間程度維持し、塗膜の乾
燥促進とセッティングを行うスピンコ−ト法により、前
記ガラス基板表面に、約25〜26℃、相対湿度約約58〜60
%RHの環境で塗布被膜し、微細な凹凸状表層を発現形成
しているゲル膜を成膜性よくそれぞれ成膜した。Next, as a spin film forming condition, a glass substrate is set on a spin coater, and first, after 1 to 3 seconds from the start of spin rotation, the rotation speed is about 150 rpm (for example, about 50 to 250 rpm).
Spinning at high speed for about pm), about 100 ml of each coating solution (coating solution) described above was dropped, and the coating was performed while maintaining the rotation speed for about 19 to 17 seconds. Next, before the coating solution formed into a film starts to dry and loses its fluidity, the spin rotation is temporarily stopped and the leveling is performed by resting for about 60 seconds.
Re-start the spin rotation, about 50 rpm (for example, about 20 to 10
(0 rpm) at a low speed for about 40 seconds to accelerate the drying and setting of the coating film on the glass substrate surface by a temperature of about 25 ~ 26 ℃, relative humidity of about 58 ~ 60
The coating film was applied in an environment of% RH, and a gel film expressing a fine uneven surface layer was formed with good film forming properties.
【0041】続いて約250 ℃で約30分間加熱仮焼成した
後、さらに雰囲気温度約720 ℃(ガラス温度約640 ℃程
度)で約4分間加熱本焼成し、膜厚約120 〜135nm の S
iO2-TiO2薄膜を有する薄膜をそれぞれ得た。なお当該仮
焼成段階で溶媒や有機物が蒸発または分解し膜の硬さが
増大し、さらに本焼成で有機物、アルキル基、アルコキ
シル基等の分解が進み、膜硬度は飛躍的に増大するが、
場合によっては前記仮焼成段階は必ずしも必要としな
い。Subsequently, after calcination by heating at about 250 ° C. for about 30 minutes, main calcination at ambient temperature of about 720 ° C. (glass temperature of about 640 ° C.) for about 4 minutes is performed to obtain an S film having a thickness of about 120 to 135 nm.
Thin films with iO 2 -TiO 2 thin films were obtained respectively. Note that the solvent or organic matter is evaporated or decomposed in the calcination stage to increase the hardness of the film, and further the main calcination progresses the decomposition of the organic matter, the alkyl group, the alkoxyl group, etc., and the film hardness is dramatically increased.
In some cases, the calcination step is not always necessary.
【0042】得られたそれぞれのゾルゲル膜(下地層)
の評価を下記のように行った。
〔表層表面形状の観察〕上記したように、 1,3-BDOの添
加量を0wt%、2.5 wt%、4wt%、5wt%、7.5 wt%、
10wt%、15wt%、20wt%、30wt%と変えた塗布溶液で成
膜し得られたそれぞれのゾルゲル膜について、走査型プ
ロ−ブ顕微鏡のAFM (原子間力電子顕微鏡)モ−ド(セ
イコ−電子製、SPI3700 、5 μm 四方スキャンあるいは
オリンパス製、NV2000、5 μm 四方スキャン)によって
表面形状状態を観察し、写真に撮影するとともに、JIS
B 0601で定義されている中心線平均粗さRaを、測定面に
対し適用し三次元に拡張したもので、「基準面から指定
面までの偏差の絶対値を平均した値」と表現でき、次式
で与えられる平均面粗さRa' 値(nm)を求めた。Each of the obtained sol-gel films (underlayer)
Was evaluated as follows. [Observation of Surface Surface Topography] As described above, the addition amounts of 1,3-BDO were 0 wt%, 2.5 wt%, 4 wt%, 5 wt%, 7.5 wt%,
AFM (atomic force electron microscope) mode (seiko-mode) of a scanning probe microscope was used for each sol-gel film obtained by coating with different coating solutions of 10 wt%, 15 wt%, 20 wt% and 30 wt%. Electron, SPI3700, 5 μm square scan or Olympus, NV2000, 5 μm square scan) to observe the surface shape condition and take a photograph.
The center line average roughness Ra defined by B 0601 is applied to the measurement surface and expanded three-dimensionally, and it can be expressed as "the value obtained by averaging the absolute values of the deviations from the reference surface to the specified surface". The average surface roughness Ra 'value (nm) given by the following formula was determined.
【0043】[0043]
【数1】 [Equation 1]
【0044】式中、Ra' 値:平均面粗さ(nm)、S0:測
定面が理想的にフラットであるとした時の面積|X R −
X L |×|Y T −Y B |、F(X,Y):測定点(X,Y)におけ
る高さ、X L 、X R 、Y B 、Y T :X 座標、Y 座標の測
定範囲、Z0:測定面内の平均高さを表す。In the equation, Ra ′ value: average surface roughness (nm), S 0 : area where the measuring surface is ideally flat | X R −
X L | × | Y T −Y B |, F (X, Y): Height at measurement point (X, Y), XL , X R , Y B , Y T : X coordinate, Y coordinate measurement range , Z 0 : Shows the average height in the measurement plane.
【0045】その結果、ゾルゲル膜における 1,3-BDOの
添加量0wt%、2.5 wt%、4wt%、5wt%、7.5 wt%、
10wt%、15wt%、20wt%、30wt%に対する平均面粗さR
a' 値(nm)の関係について表1および図1に示す。ま
た 1,3-BDOの添加量4wt%のゾルゲル膜の表面形状をAF
M の写真である図2に示す。As a result, the addition amount of 1,3-BDO in the sol-gel film was 0 wt%, 2.5 wt%, 4 wt%, 5 wt%, 7.5 wt%,
Average surface roughness R for 10wt%, 15wt%, 20wt%, 30wt%
The relationship between the a'value (nm) is shown in Table 1 and FIG. In addition, the surface shape of the sol-gel film with the addition amount of 1,3-BDO of 4 wt% is AF
It is shown in FIG. 2, which is a photograph of M.
【0046】1,3-BDOの添加量0〜30wt%に対しそれぞ
れのゾルゲル膜の平均面粗さRa' 値が2〜15.8nmとな
り、好ましくは該添加量が 0.5〜30wt%に対しRa' 値が
2.5〜15.8nmであるが、明らかに所期の微細な凹凸状表
層となっていた。When the amount of 1,3-BDO added is 0 to 30 wt%, the average surface roughness Ra ′ of each sol-gel film is 2 to 15.8 nm, preferably Ra ′ is 0.5 to 30 wt%. value
Although it is 2.5 to 15.8 nm, it was clearly the desired fine uneven surface layer.
【0047】なお、より好ましいRa' 値としては4〜15
nm程度、最も好ましいRa' 値としては6〜10nm程度であ
る。
〔初期ヘイズ(曇価)値H%〕表1に示すように、ヘイ
ズメ−タ−による測定でそれぞれのゾルゲル膜の初期ヘ
イズ値H%が約0.1 〜0.3 %であり、ガラス基板並で良
好であった。
〔耐摩耗性〕表1に示すように、 テ−バ−摩耗試験に
おいて、それぞれのゾルゲル膜の膜強度が摩耗輪CS-10F
で20回転後のヘイズ値の増加分△H=0.1 〜0.3 %であ
り、ガラス基板並の膜硬度を示しきわめて良好であっ
た。A more preferable Ra 'value is 4 to 15
nm, and the most preferable Ra 'value is about 6 to 10 nm. [Initial haze (haze value) value H%] As shown in Table 1, the initial haze value H% of each sol-gel film measured by a haze meter is about 0.1 to 0.3%, which is as good as that of a glass substrate. there were. [Abrasion resistance] As shown in Table 1, in the Taber abrasion test, the film strength of each sol-gel film was compared with that of the abrasion wheel CS-10F.
The increase in the haze value after 20 rotations was ΔH = 0.1 to 0.3%, and the film hardness was as good as that of a glass substrate and was very good.
【0048】これらから該ゾルゲル膜は、成膜環境に高
湿を必ずしも必要とせず、かつ調合調製の温度や時間を
増大させる必要もなく、短く簡便な調合調製で凹凸状面
形状を制御性よく安定かつ確実に発現せしめることがで
き、しかも低反射膜としてまた撥水性ガラスの下地層等
として自動車用ドアならびにフロントおよびバック窓ガ
ラスに対し充分耐えて採用しうるものである。From these facts, the sol-gel film does not necessarily require high humidity in the film forming environment and does not need to increase the temperature and time for preparation and preparation, and the shape of the uneven surface can be controlled with good control by a short and simple preparation. It can be stably and surely exhibited, and can be used as a low reflection film and as an underlayer of water-repellent glass while sufficiently enduring against automobile doors and front and back window glasses.
【0049】[0049]
【表1】 [Table 1]
【0050】実施例2
実施例1と同様なガラス基板に、実施例1の1,3-BDO と
1,2-BDO ならびに1,4-BDO のブタンジオ─ル類を添加量
3wt%用い、他は実施例1と同様に溶液AとBを得た。
次いで攪拌条件等実施例1と同様に調製しコーテイング
溶液とした。 Example 2 A glass substrate similar to that of Example 1 was mixed with 1,3-BDO of Example 1 and
Solutions A and B were obtained in the same manner as in Example 1 except that 1,2-BDO and 1,4-BDO butanediols were added in an amount of 3 wt%.
Then, stirring conditions and the like were prepared in the same manner as in Example 1 to obtain a coating solution.
【0051】次いで、実施例1と同様の成膜法で成膜し
た。得られた膜厚約120nm 程度のSiO2-TiO2 薄膜は、該
ゾルゲル膜の表面形状状態を実施例1と同様の評価をし
た。Next, a film was formed by the same film forming method as in Example 1. The obtained SiO 2 —TiO 2 thin film having a thickness of about 120 nm was evaluated for the surface shape of the sol-gel film in the same manner as in Example 1.
【0052】その結果、ブタンジオ─ル類のOH基の位置
が及ぼす影響を表2に示すように、平均面粗さRa' 値が
約4〜6.2nm となり、初期ヘイズ値Hは約0.1 %程度で
あり、テ−バ−摩耗試験後の△Hは約0.2 %程度と膜硬
度もガラス基板並であり、実施例1と同様の微細な凹凸
状表層を示し、低反射膜としてまた撥水性ガラスの下地
層等として自動車用ドアならびにフロントおよびバック
窓ガラスに対し充分耐えて採用しうるものである。As a result, as shown in Table 2, the influence of the position of the OH group of butanediol is shown in Table 2. The average surface roughness Ra 'is about 4 to 6.2 nm and the initial haze value H is about 0.1%. The ΔH after the Taber abrasion test is about 0.2% and the film hardness is comparable to that of the glass substrate, and the fine uneven surface layer similar to that of Example 1 is shown, and the low-reflection film is also water-repellent glass. It can be used as a base layer, etc. while sufficiently enduring against automobile doors and front and back window glasses.
【0053】[0053]
【表2】 [Table 2]
【0054】実施例3
実施例1と同様なガラス基板に、実施例1の1,3-BDO に
替えてエチレングリコ−ル、1,3-プロパンジオ−ル、1,
4-BDO 、1,5-ペンタンジオ−ルのジオ─ル類を添加量3
wt%用い、他は実施例1と同様に溶液AとBを得た。次
いで攪拌条件等他は実施例1と同様に調製しコーテイン
グ溶液とした。 Example 3 On the same glass substrate as in Example 1, 1,3-BDO in Example 1 was replaced by ethylene glycol, 1,3-propanediol, 1,
4-BDO, 1,5-pentanediol diols added 3
Solution A and B were obtained in the same manner as in Example 1 except that wt% was used. Next, stirring conditions and the like were prepared in the same manner as in Example 1 to obtain a coating solution.
【0055】次いで、実施例1と同様の成膜法で成膜し
た。得られた膜厚約120nm 程度のSiO2-TiO2 薄膜は、該
ゾルゲル膜の表面形状状態を実施例1と同様の評価をし
た。Then, a film was formed by the same film forming method as in Example 1. The obtained SiO 2 —TiO 2 thin film having a thickness of about 120 nm was evaluated for the surface shape of the sol-gel film in the same manner as in Example 1.
【0056】その結果、種々のジオ−ル類の添加効果を
表3に、また直鎖ジオ−ルのメチレン基の数と平均面粗
さRa' 値の関係を図3に示すように、平均面粗さRa' 値
が約9.4 〜4.8nm となり、初期ヘイズ値Hは約0.1 %程
度であり、テ−バ−摩耗試験後の△Hは約0.2 %程度と
膜硬度もガラス基板並であり、実施例1と同様の微細な
凹凸状表層を示し、低反射膜としてまた撥水性ガラスの
下地層等として自動車用ドアならびにフロントおよびバ
ック窓ガラスに対しては充分耐えて採用しうるものであ
る。As a result, the effect of adding various diols is shown in Table 3, and the relationship between the number of methylene groups in the straight-chain diol and the average surface roughness Ra 'value is shown in FIG. The surface roughness Ra 'value is about 9.4 to 4.8 nm, the initial haze value H is about 0.1%, the ΔH after the Taber abrasion test is about 0.2%, and the film hardness is similar to that of the glass substrate. The same fine uneven surface layer as that of Example 1 is shown, and it can be used as a low reflection film and as an underlayer of water-repellent glass while being sufficiently resistant to automobile doors and front and back window glasses. .
【0057】[0057]
【表3】 [Table 3]
【0058】実施例4
実施例1と同様なガラス基板に、実施例1のテトラブト
キシチタン〔Ti(O-Bu) 4 〕に替えてトリブトキシアルミ
ニウム〔Al(O-Bu)3 〕を用い、他は実施例1と同様に溶
液AとBを得た。次いで攪拌条件のみ約30℃で約6時間
(蜜封)と替え他は実施例1と同様に調製しコーテイン
グ溶液とした。[0058]Example 4
On the same glass substrate as in Example 1, the tetrabutane of Example 1 was added.
Xytitanium (Ti (O-Bu) Four] In place of tributoxy aluminum
Nium (Al (O-Bu)3], And the same as in Example 1 except that
Liquids A and B were obtained. Next, only stirring conditions at about 30 ℃ for about 6 hours
Preparation with the same procedure as in Example 1 except for (honey sealed)
Solution.
【0059】次いで、環境湿度のみ約53%RHと替えたの
みで、実施例1と同様の成膜法で成膜した。得られた膜
厚約74nm程度の Al2O3・SiO2薄膜は、該ゾルゲル膜の表
面形状状態を実施例1と同様の評価をした。Then, only the ambient humidity was changed to about 53% RH, and a film was formed by the same film forming method as in Example 1. The obtained Al 2 O 3 .SiO 2 thin film having a thickness of about 74 nm was evaluated for the surface shape of the sol-gel film in the same manner as in Example 1.
【0060】その結果、実施例1と同様の微細な凹凸状
表層を示し、初期ヘイズ値Hは約0.1 %程度であり、テ
−バ−摩耗試験後の△Hは約0.6 程度と膜硬度がやや劣
るものの、低反射膜としてまた撥水性ガラスの下地層等
として自動車用ドアならびにフロントおよびバック窓ガ
ラスに対しては充分耐えて採用しうるものである。As a result, the same fine concavo-convex surface layer as in Example 1 was shown, the initial haze value H was about 0.1%, and ΔH after the Taber abrasion test was about 0.6, indicating that the film hardness was about 0.6%. Although somewhat inferior, it can be used as a low-reflection film and as an underlayer of water-repellent glass, with sufficient durability against automobile doors and front and back window glasses.
【0061】[0061]
【発明の効果】以上前述したように、本発明によれば、
特定量のジオ−ル類の添加したコ−ティング溶液とした
ことにより、より簡単に調合調製できかつ飛躍的な安定
性および性能を発揮し、より簡便に容易な膜形成手段で
もって特異な薄膜を安価に効率よく得られ、特定の二つ
を選択したゾル溶液ならびに希釈溶液を巧みに組み合わ
せることによって、比表面積をより増大して特異な形状
を有する強固な微細な凹凸状表層が安定かつ確実に制御
性よく得られるようになり、多層膜の下地層薄膜として
格段にその性能を発揮し、その表面に優れた撥水性能薄
膜等各種機能性薄膜を被膜して、光学特性を損なうこと
なく、撥水性能等各種性能が優れることはもとより、密
着性、ことに機械的強度、耐候性等の耐久性を格段に優
れるものとし、建築用もしくは自動車用の各種窓材をは
じめ、船舶や航空機の窓材など各種ガラス物品等、種々
の被覆膜に広く採用できる利用価値の高い、有用な微細
な凹凸状表層を有するゾルゲル膜およびその形成法を提
供するものである。As described above, according to the present invention,
By using a coating solution to which a specific amount of diols has been added, it is possible to easily formulate and prepare, and to exhibit dramatic stability and performance, and a unique thin film with a simple and easy film forming means. Can be obtained inexpensively and efficiently, and by skillfully combining the sol solution and the dilute solution selected from the two specific ones, the specific surface area can be increased and a strong fine uneven surface layer with a unique shape is stable and reliable. It is possible to obtain excellent controllability, and it exhibits its performance remarkably as an underlayer thin film of a multilayer film, and various functional thin films such as excellent water-repellent performance thin films are coated on the surface without impairing optical characteristics. In addition to excellent water repellency and other properties, it is also markedly superior in adhesion, especially in mechanical strength and durability such as weather resistance. Like a window material such as various glass articles, high utility value that can be widely adopted in a variety of coating, there is provided a sol-gel film and its forming method have useful finely uneven surface.
【図1】実施例1における、1,3-BDO の添加量とゾルゲ
ル膜の平均面粗さRa' 値との関係を示す図である。FIG. 1 is a graph showing the relationship between the amount of 1,3-BDO added and the average surface roughness Ra ′ value of a sol-gel film in Example 1.
【図2】実施例1における、1,3-BDO の添加量が4wt%
である本発明のゾルゲル膜の表面形状を、原子間力電子
顕微鏡(AFM )により観察処理した写真であって、微細
な凹凸状表層の状態を示す図である。2] In Example 1, the amount of 1,3-BDO added was 4 wt%.
FIG. 3 is a photograph of the surface shape of the sol-gel film of the present invention, which is observed by an atomic force electron microscope (AFM), showing a state of a fine uneven surface layer.
【図3】実施例3における、直鎖ジオ−ルのメチレン基
の数と平均面粗さRa' 値との関係を示す図である。FIG. 3 is a diagram showing the relationship between the number of methylene groups of linear diol and the average surface roughness Ra ′ value in Example 3.
フロントページの続き (56)参考文献 特開 平6−298545(JP,A) (58)調査した分野(Int.Cl.7,DB名) C03C 15/00 - 23/00 B32B 1/00 - 35/00 B60J 1/00 Continuation of the front page (56) Reference JP-A-6-298545 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) C03C 15/00-23/00 B32B 1/00-35 / 00 B60J 1/00
Claims (8)
で安定化した金属アルコキシドを添加したテトラアルコ
キシシランを加水分解ならびに脱水縮合させたゾル溶液
Aと、1つの官能基をアルキル基化したアルキルトリア
ルコキシシランを加水分解ならびに脱水縮合したゾル溶
液Bとを混合した混合物と、イソプロピルアルコ−ルを
主成分とする溶媒と、添加量が、コ−ティング溶液中の
全ての金属アルコキシドの合計固形分に対し、0.5〜
30wt%であるジオ−ル類と、からなるコ−ティング
溶液を被覆し、加熱焼成することで得る微細な凹凸状表
層を有する酸化物薄膜で成ることを特徴とするゾルゲル
膜。1. A sol solution A obtained by hydrolyzing and dehydrating and condensing a tetraalkoxysilane to which a metal alkoxide stabilized with acetylacetone is added on the surface of a glass substrate, and an alkyltrialkoxy in which one functional group is an alkyl group. The mixture of the sol solution B obtained by hydrolyzing and dehydrating and condensing silane, the solvent containing isopropyl alcohol as a main component, and the addition amount of the sol solution B in the coating solution are
0.5 to the total solid content of all metal alkoxides
A sol-gel film comprising an oxide thin film having a fine uneven surface layer obtained by coating a coating solution containing 30 wt% of diols and heating and baking.
おける平均面粗さRa'値が、2.5 〜15.8nmであ
ることを特徴とする請求項1記載のゾルゲル膜。2. The sol-gel film according to claim 1, wherein an average surface roughness Ra ′ value on the surface of the fine rugged surface layer of the sol-gel film is 2.5 to 15.8 nm.
1又は2記載のゾルゲル膜。 3. Use as an underlayer of a functional multilayer film.
The sol-gel film according to 1 or 2.
1又は2記載のゾルゲル膜。 4. Use as an underlayer of water-repellent glass.
The sol-gel film according to 1 or 2.
求項1又は2記載のゾルゲル膜。 5. A contract characterized by being used as a low reflection film.
The sol-gel film according to claim 1 or 2.
で安定化した金属アルコキシドを添加したテトラアルコ
キシシランを加水分解ならびに脱水縮合させたゾル溶液
Aと、1つの官能基をアルキル基化したアルキルトリア
ルコキシシランを加水分解ならびに脱水縮合したゾル溶
液Bとを混合し、ジオール類の添加量が、コ−ティング
溶液中の金属アルコキシドの固形分に対し、0.5〜3
0wt%になるようにジオ−ル類を添加したアルコ─ル
系溶媒で適度の希釈をし、10℃乃至50℃の保持温度
で1乃至24時間攪拌した混合物を作製し、該混合物を
イソプロピルアルコ−ルを主成分とする溶媒で希釈し調
製してなるコ−ティング溶液を被膜し、乾燥加熱焼成し
微細な凹凸状表層を有する酸化物薄膜で成るようにする
ことを特徴とするゾルゲル膜の形成法。6. A sol solution A obtained by hydrolyzing and dehydrating and condensing a tetraalkoxysilane containing a metal alkoxide stabilized with acetylacetone on the surface of a glass substrate, and an alkyltrialkoxy having one functional group alkylated. The sol solution B obtained by hydrolyzing and dehydrating and condensing silane was mixed, and the amount of diols added was changed to the coating amount.
0.5 to 3 based on the solid content of the metal alkoxide in the solution
The mixture was appropriately diluted with an alcohol solvent to which diols were added so as to be 0 wt% and stirred at a holding temperature of 10 ° C to 50 ° C for 1 to 24 hours to prepare a mixture, and the mixture was mixed with isopropyl alcohol. Of a sol-gel film, characterized by comprising coating a coating solution prepared by diluting with a solvent having a main component, and drying and heating to form an oxide thin film having a fine uneven surface layer. Forming method.
が、酸化物換算で0.2〜5.0wt%になるよう希釈
調製することを特徴とする請求項6に記載のゾルゲル膜
の形成法。7. The method for forming a sol-gel film according to claim 6, wherein the coating solution is diluted to a solid content concentration of 0.2 to 5.0 wt% in terms of oxide. .
CPに粘度調整することでなるコーテイング溶液とする
ことを特徴とする請求項6又は請求項7記載のゾルゲル
膜の形成法。8. The viscosity of the coating solution is 1-10.
The method for forming a sol-gel film according to claim 6 or 7, wherein the coating solution is prepared by adjusting the viscosity of CP.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13387896A JP3385159B2 (en) | 1996-05-28 | 1996-05-28 | Sol-gel film and method for forming the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13387896A JP3385159B2 (en) | 1996-05-28 | 1996-05-28 | Sol-gel film and method for forming the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH09315839A JPH09315839A (en) | 1997-12-09 |
| JP3385159B2 true JP3385159B2 (en) | 2003-03-10 |
Family
ID=15115198
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13387896A Expired - Fee Related JP3385159B2 (en) | 1996-05-28 | 1996-05-28 | Sol-gel film and method for forming the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3385159B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005227443A (en) * | 2004-02-12 | 2005-08-25 | Konica Minolta Opto Inc | Reflection preventive film, polarizing plate and liquid crystal display device |
| JP4604927B2 (en) * | 2005-09-12 | 2011-01-05 | セイコーエプソン株式会社 | Liquid crystal device, method for manufacturing liquid crystal device, and projection display device |
| CN114105488A (en) * | 2020-08-26 | 2022-03-01 | 上海西源新能源技术有限公司 | Neutral color double-layer anti-reflection coating, glass with the coating and preparation method thereof |
-
1996
- 1996-05-28 JP JP13387896A patent/JP3385159B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH09315839A (en) | 1997-12-09 |
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