JP3744061B2 - Permeable pavement material - Google Patents
Permeable pavement material Download PDFInfo
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- JP3744061B2 JP3744061B2 JP16864596A JP16864596A JP3744061B2 JP 3744061 B2 JP3744061 B2 JP 3744061B2 JP 16864596 A JP16864596 A JP 16864596A JP 16864596 A JP16864596 A JP 16864596A JP 3744061 B2 JP3744061 B2 JP 3744061B2
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T30/00—Transportation of goods or passengers via railways, e.g. energy recovery or reducing air resistance
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- Application Of Or Painting With Fluid Materials (AREA)
- Road Paving Structures (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Tents Or Canopies (AREA)
- Eyeglasses (AREA)
- Surface Treatment Of Optical Elements (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、多孔質セラミックからなる透水性舗装材に関する。より詳しくは、本発明は、汚れが付着しにくく、降雨により気孔が自己浄化されるようになった透水性舗装材に関する。
【0002】
【従来の技術】
歩道、ベランダ、ポーチ、プールサイドのように雨水のかかる場所の舗装には、多孔質セラミックからなる透水性の舗装材が使用されており、雨水を大地に滲み込ませて水はけを良くすることにより、滑りを防止し、或いは凍結を防止するようになっている。
例えば、特開昭60-171972号、特開昭63-260876号、特開昭64-42372号に開示されているように、この種の透水性舗装材は、抗火石、高炉スラグ、陶器廃材などの骨材の粒子をガラス、フリット、長石などの無機バインダーで結着することにより製造され、骨材粒子間には雨水の透過を可能にする微小な連続気孔が形成されている。
【0003】
【発明が解決しようとする課題】
環境汚染に伴い、都市部では透水性舗装材の汚れが顕著になっている。透水性舗装材の気孔には都市煤塵中のカーボンブラックのような親油性の汚染物質が付着するので、舗装材の美観を損ねるだけでなく、気孔の目詰まりにより舗装材の透水性を低下させる。
本発明の目的は、優れた透水性を長期間にわたり維持することの可能な透水性舗装材を提供することにある。
【0004】
【課題を解決するための手段】
本発明者は、光触媒を光励起すると光触媒の表面が高度に親水化されることを発見した。
本発明は斯る発見に基づくもので、透水性舗装材の表面近傍に位置する気孔の内周面を半導体光触媒を含有する層によって被覆したことを特徴とするものである。
舗装材は昼間は太陽の照射を受け、舗装材の表面近傍に位置する光触媒は太陽光によって光励起される。光励起に伴い、光触媒含有層の表面は水との接触角が10゜以下、より詳しくは5゜以下、特に約0゜になる程度に高度に親水化される。一旦高度に親水化されると、表面の親水性は夜間でも持続する。
【0005】
このように高度に親水化された表面には、都市煤塵中のカーボンブラックのような親油性の汚染物質は付着しにくい。また、超親水性の表面は空気中の湿分を吸着しやすく、静電気的に帯電しないので、煤塵が付着しにくい。
更に、舗装材は時々降雨にさらされる。超親水化された表面の水に対する親和力は、カーボンブラックのような親油性の汚染物質に対する親和力よりも大きいので、気孔の内周面に付着した汚れは雨水により表面から容易に釈放され、降雨の都度雨水によって洗い流され、気孔の内周面は自己浄化(セルフクリーニング)される。
【0006】
【発明の実施の形態】
図1を参照するに、透水性舗装材10は多孔質セラミックからなり、この多孔質セラミックは、抗火石、高炉スラグ、陶器廃材などの骨材の粒子12をガラス、フリット、長石などの無機バインダー14で結着することにより形成されている。骨材粒子12間には微小な連続気孔16が形成されており、舗装材10に透水性を与えている。
【0007】
図2の拡大図を参照するに、気孔16の内周面は半導体光触媒の粒子を含有する層18によってコーティングしてある。光触媒含有層18の厚さは約0.1μm以下で充分である。
【0008】
光触媒としては、チタニア(TiO2)が最も好ましい。チタニアは、無害であり、かつ、化学的に安定である。アナターゼ型チタニアとルチル型チタニアのいづれも使用することができる。
光触媒性チタニアを紫外線によって光励起すると、光触媒作用によって水が水酸基(OH-)の形で表面に化学吸着され、その結果、表面が超親水性になると考えられる。使用可能な他の光触媒としては、ZnO、SnO2、SrTiO3、WO3、Bi2O3、Fe2O3のような金属酸化物がある。これらの金属酸化物は、チタニアと同様に、表面に金属元素と酸素が存在するので、表面水酸基(OH-)を吸着しすいと考えられる。
【0009】
本発明の第1実施態様においては、光触媒含有層18はシリカ配合チタニアによって形成される。チタニアとシリカとの合計に対するシリカの割合は、5〜90モル%、好ましくは10〜70モル%、より好ましくは10〜50モル%にすることができる。シリカ配合チタニアからなる光触媒含有層18の形成には、次のいづれかの方法を採用することができる。
(1)アナターゼ型又はルチル型チタニアの粒子とシリカの粒子とを含む懸濁液をスプレーコーティング又はディップコーティングにより舗装材の表面と表面近傍の気孔16の内周面に塗布し、約700℃の温度で焼成する。
【0010】
(2)無定形シリカの前駆体(例えば、テトラエトキシシラン、テトライソプロポキシシラン、テトラn−プロポキシシラン、テトラブトキシシラン、テトラメトキシシラン、等のテトラアルコキシシラン;それらの加水分解物であるシラノール; 又は平均分子量3000以下のポリシロキサン)と結晶性チタニアゾルとの混合物をスプレーコーティング又はディップコーティングにより舗装材の表面と表面近傍の気孔の内周面に塗布し、必要に応じて加水分解させてシラノールを形成した後、約100℃以上の温度で加熱してシラノールを脱水縮重合に付すことにより、チタニアが無定形シリカで結着された光触媒含有層を形成する。特に、シラノールの脱水縮重合を約200℃以上の温度で行えば、シラノールの重合度を増し、光触媒含有層の耐アルカリ性能を向上させることができる。
【0011】
(3)無定形チタニアの前駆体(チタンのアルコキシド、キレート、又はアセテートのような有機チタン化合物、又はTiCl4又はTi(SO4)2のような無機チタン化合物)の溶液にシリカの粒子を分散させてなる懸濁液をスプレーコーティング又はディップコーティングにより舗装材の表面と表面近傍の気孔の内周面に塗布し、チタン化合物を常温から200℃の温度で加水分解と脱水縮重合に付すことにより、シリカ粒子が分散された無定形チタニアの薄膜を形成する。次いで、舗装材を約700℃の温度に加熱することにより、無定形チタニアを結晶性チタニアに相変化させる。
【0012】
(4)無定形チタニアの前駆体(チタンのアルコキシド、キレート、又はアセテートのような有機チタン化合物、又はTiCl4又はTi(SO4)2のような無機チタン化合物)の溶液に無定形シリカの前駆体(例えば、テトラエトキシシラン、テトライソプロポキシシラン、テトラn−プロポキシシラン、テトラブトキシシラン、テトラメトキシシラン、等のテトラアルコキシシラン;それらの加水分解物であるシラノール; 又は平均分子量3000以下のポリシロキサン)を混合し、スプレーコーティング又はディップコーティングにより舗装材の表面と表面近傍の気孔の内周面に塗布する。次いで、これらの前駆体を加水分解と脱水縮重合に付すことにより、無定形チタニアと無定形シリカの混合物からなる薄膜を形成する。次いで、舗装材を約700℃の温度に加熱することにより、無定形チタニアを結晶性チタニアに相変化させる。
【0013】
本発明の他の実施態様においては、光触媒含有層18は、シリコーン(オルガノポリシロキサン)にアナターゼ型チタニアなどの光触媒の粒子を50重量%以下の割合で分散させることにより形成することができる。このため、未硬化の若しくは部分的に硬化したシリコーン又はシリコーンの前駆体からなる塗膜形成要素にチタニアの粒子を分散させてなる塗料用組成物を用いることができる。
【0014】
塗膜形成要素としては、メチルトリクロルシラン、メチルトリブロムシラン、メチルトリメトキシシラン、メチルトリエトキシシラン、メチルトリイソプロポキシシラン、メチルトリt−ブトキシシラン;エチルトリクロルシラン、エチルトリブロムシラン、エチルトリメトキシシラン、エチルトリエトキシシラン、エチルトリイソプロポキシシラン、エチルトリt−ブトキシシラン;n−プロピルトリクロルシラン、n−プロピルトリブロムシラン、n−プロピルトリメトキシシラン、n−プロピルトリエトキシシラン、n−プロピルトリイソプロポキシシラン、n−プロピルトリt−ブトキシシラン;n−ヘキシルトリクロルシラン、n−ヘキシルトリブロムシラン、n−ヘキシルトリメトキシシラン、n−ヘキシルトリエトキシシラン、n−ヘキシルトリイソプロポキシシラン、n−ヘキシルトリt−ブトキシシラン;n−デシルトリクロルシラン、n−デシルトリブロムシラン、n−デシルトリメトキシシラン、n−デシルトリエトキシシラン、n−デシルトリイソプロポキシシラン、n−デシルトリt−ブトキシシラン;n−オクタデシルトリクロルシラン、n−オクタデシルトリブロムシラン、n−オクタデシルトリメトキシシラン、n−オクタデシルトリエトキシシラン、n−オクタデシルトリイソプロポキシシラン、n−オクタデシルトリt−ブトキシシラン;フェニルトリクロルシラン、フェニルトリブロムシラン、フェニルトリメトキシシラン、フェニルトリエトキシシラン、フェニルトリイソプロポキシシラン、フェニルトリt−ブトキシシラン;テトラクロルシラン、テトラブロムシラン、テトラメトキシシラン、テトラエトキシシラン、テトラブトキシシラン、ジメトキシジエトキシシラン;ジメチルジクロルシラン、ジメチルジブロムシラン、ジメチルジメトキシシラン、ジメチルジエトキシシラン;ジフェニルジクロルシラン、ジフェニルジブロムシラン、ジフェニルジメトキシシラン、ジフェニルジエトキシシラン;フェニルメチルジクロルシラン、フェニルメチルジブロムシラン、フェニルメチルジメトキシシラン、フェニルメチルジエトキシシラン;トリクロルヒドロシラン、トリブロムヒドロシラン、トリメトキシヒドロシラン、トリエトキシヒドロシラン、トリイソプロポキシヒドロシラン、トリt−ブトキシヒドロシラン;ビニルトリクロルシラン、ビニルトリブロムシラン、ビニルトリメトキシシラン、ビニルトリエトキシシラン、ビニルトリイソプロポキシシラン、ビニルトリt−ブトキシシラン;トリフルオロプロピルトリクロルシラン、トリフルオロプロピルトリブロムシラン、トリフルオロプロピルトリメトキシシラン、トリフルオロプロピルトリエトキシシラン、トリフルオロプロピルトリイソプロポキシシラン、トリフルオロプロピルトリt−ブトキシシラン;γ−グリシドキシプロピルメチルジメトキシシラン、γ−グリシドキシプロピルメチルジエトキシシラン、γ−グリシドキシプロピルトリメトキシシラン、γ−グリシドキシプロピルトリエトキシシラン、γ−グリシドキシプロピルトリイソプロポキシシラン、γ−グリシドキシプロピルトリt−ブトキシシラン;γ−メタアクリロキシプロピルメチルジメトキシシラン、γ−メタアクリロキシプロピルメチルジエトキシシラン、γ−メタアクリロキシプロピルトリメトキシシラン、γ−メタアクリロキシプロピルトリエトキシシラン、γ−メタアクリロキシプロピルトリイソプロポキシシラン、γ−メタアクリロキシプロピルトリt−ブトキシシラン;γ−アミノプロピルメチルジメトキシシラン、γ−アミノプロピルメチルジエトキシシラン、γ−アミノプロピルトリメトキシシラン、γ−アミノプロピルトリエトキシシラン、γ−アミノプロピルトリイソプロポキシシラン、γ−アミノプロピルトリt−ブトキシシラン;γ−メルカプトプロピルメチルジメトキシシラン、γ−メルカプトプロピルメチルジエトキシシラン、γ−メルカプトプロピルトリメトキシシラン、γ−メルカプトプロピルトリエトキシシラン、γ−メルカプトプロピルトリイソプロポキシシラン、γ−メルカプトプロピルトリt−ブトキシシラン;β−(3、4−エポキシシクロヘキシル)エチルトリメトキシシラン、β−(3、4−エポキシシクロヘキシル)エチルトリエトキシシラン; それらの部分加水分解物;およびそれらの混合物を使用することができる。
【0015】
この塗料用組成物を舗装材の表面と表面近傍の気孔の内周面に塗布し、約100℃〜200℃の温度でシリコーンを硬化させる。この舗装材を用いて歩道などの舗装を施工すると、舗装材は昼間は太陽の照射を受け、舗装材の表面近傍に位置する光触媒は太陽光によって光励起される。光励起に伴い、光触媒の作用により光触媒含有シリコーン層18の表面にはシリコーン分子のケイ素原子に結合した有機基が少なくとも部分的に水酸基に置換されたシリコーン誘導体が形成され、シリコーン層の表面は水との接触角が約0゜になる程度に超親水化される。
【0016】
このように高度に親水化された光触媒含有層18の表面には、都市煤塵中のカーボンブラックのような親油性の汚染物質は付着しにくい。また、超親水化された光触媒含有層18の表面は空気中の湿分を吸着し、静電気による帯電が生じないので、煤塵が静電気的に付着しにくい。更に、泥や土のような無機物質の水との接触角は20゜から50゜であるので、水との接触角が約0゜になる程度に超親水化された光触媒含有層18には泥や土のような無機塵埃は付着しにくい。
超親水化された表面の水に対する親和力はカーボンブラックのような親油性の汚染物質に対する親和力よりも大きいので、舗装材が降雨にさらされると、気孔の内周面に付着した汚れは雨水により表面から釈放され、雨水によって洗い流され、気孔の内周面は自己浄化される。
その結果、気孔の目詰まりが防止され、舗装材は長期間にわたり優れた透水性を維持する。
【0017】
本発明の更に他の実施態様においては、舗装材は、骨材の粒子12を予め光触媒含有層18で被覆し、ガラス、フリット、長石などの無機バインダーと混練した後成形し、約700℃の温度で焼成することにより形成することができる。
【0018】
【発明の効果】
本発明によれば、透水性舗装材の気孔に汚れが付着するのが防止されると共に、気孔の内周面に付着した汚れは降雨の都度雨水によって洗い流され、気孔はセルフクリーニングされるので、舗装材の透水性を長期間にわたり維持することができる。
【図面の簡単な説明】
【図1】本発明の透水性舗装材の模式的拡大断面図である。
【図2】図1に示した舗装材の一部を更に拡大した断面図である。
【符号の説明】
10: 透水性舗装材
16: 気孔
18: 光触媒含有層[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a water-permeable pavement material made of porous ceramic. More specifically, the present invention relates to a water-permeable pavement material in which dirt is difficult to adhere and pores are self-purified by rainfall.
[0002]
[Prior art]
Water-permeable pavement materials made of porous ceramics are used for pavement where rainwater is exposed, such as sidewalks, verandas, porches, and poolsides, and rainwater is soaked into the ground to improve drainage. , Preventing slipping or freezing.
For example, as disclosed in JP-A-60-171972, JP-A-63-260876, and JP-A-64-42372, this type of water-permeable pavement material includes anti-fluorite, blast furnace slag, and waste ceramic materials. Aggregate particles such as glass, frit, feldspar and the like are produced by binding, and minute continuous pores that allow permeation of rainwater are formed between the aggregate particles.
[0003]
[Problems to be solved by the invention]
Along with environmental pollution, dirt in permeable pavement materials has become prominent in urban areas. The pores of the water-permeable pavement are attached with lipophilic contaminants such as carbon black in urban dust, which not only detracts from the beauty of the pavement but also reduces the water permeability of the pavement due to clogging of the pores. .
The objective of this invention is providing the water-permeable pavement material which can maintain the outstanding water permeability over a long period of time.
[0004]
[Means for Solving the Problems]
The inventor has discovered that photoexcitation of the photocatalyst results in a highly hydrophilic surface of the photocatalyst.
The present invention is based on such discovery, and is characterized in that the inner peripheral surface of pores located in the vicinity of the surface of the water-permeable pavement is covered with a layer containing a semiconductor photocatalyst.
The pavement is irradiated with the sun during the daytime, and the photocatalyst located near the surface of the pavement is photoexcited by sunlight. With photoexcitation, the surface of the photocatalyst-containing layer is highly hydrophilized so that the contact angle with water is 10 ° or less, more specifically 5 ° or less, and particularly about 0 °. Once highly hydrophilized, the surface hydrophilicity persists even at night.
[0005]
Lipophilic contaminants such as carbon black in urban dust are less likely to adhere to such highly hydrophilic surfaces. In addition, the superhydrophilic surface easily absorbs moisture in the air and is not electrostatically charged, so that dust does not easily adhere.
In addition, paving materials are sometimes exposed to rainfall. Since the affinity of the superhydrophilic surface for water is greater than the affinity for lipophilic contaminants such as carbon black, dirt adhering to the inner surface of the pores can be easily released from the surface by rainwater, and Each time it is washed away by rainwater, the inner peripheral surface of the pores is self-cleaned (self-cleaning).
[0006]
DETAILED DESCRIPTION OF THE INVENTION
Referring to FIG. 1, a water-
[0007]
Referring to the enlarged view of FIG. 2, the inner peripheral surface of the
[0008]
As the photocatalyst, titania (TiO 2 ) is most preferable. Titania is harmless and chemically stable. Either anatase-type titania or rutile-type titania can be used.
It is considered that when photocatalytic titania is photoexcited by ultraviolet rays, water is chemically adsorbed on the surface in the form of hydroxyl groups (OH − ) by photocatalysis, and as a result, the surface becomes superhydrophilic. Other photocatalysts which can be used include metal oxides such as ZnO, SnO 2, SrTiO 3, WO 3, Bi 2 O 3, Fe 2 O 3. Since these metal oxides, like titania, contain metal elements and oxygen on the surface, it is thought that surface hydroxyl groups (OH − ) should be adsorbed.
[0009]
In the first embodiment of the present invention, the photocatalyst-containing layer 18 is formed of silica-containing titania. The ratio of silica to the total of titania and silica can be 5 to 90 mol%, preferably 10 to 70 mol%, more preferably 10 to 50 mol%. Any one of the following methods can be employed to form the photocatalyst-containing layer 18 made of silica-containing titania.
(1) A suspension containing anatase-type or rutile-type titania particles and silica particles is applied by spray coating or dip coating to the surface of the pavement and the inner peripheral surface of the
[0010]
(2) Amorphous silica precursors (for example, tetraalkoxysilanes such as tetraethoxysilane, tetraisopropoxysilane, tetra n-propoxysilane, tetrabutoxysilane, tetramethoxysilane; silanols that are hydrolysates thereof; (Or polysiloxane with an average molecular weight of 3000 or less) and a crystalline titania sol are applied by spray coating or dip coating to the surface of the pavement and the inner peripheral surface of the pores near the surface, and if necessary, hydrolyzed to produce silanol. After the formation, the photocatalyst-containing layer in which titania is bound with amorphous silica is formed by heating at a temperature of about 100 ° C. or higher to subject the silanol to dehydration condensation polymerization. In particular, if dehydration condensation polymerization of silanol is carried out at a temperature of about 200 ° C. or higher, the degree of polymerization of silanol can be increased and the alkali resistance performance of the photocatalyst-containing layer can be improved.
[0011]
(3) Disperse silica particles in a solution of amorphous titania precursor (organic titanium compound such as titanium alkoxide, chelate or acetate, or inorganic titanium compound such as TiCl 4 or Ti (SO 4 ) 2 ). By applying the resulting suspension to the surface of the pavement and the inner surface of the pores near the surface by spray coating or dip coating, and subjecting the titanium compound to hydrolysis and dehydration condensation polymerization at temperatures from room temperature to 200 ° C. Then, an amorphous titania thin film in which silica particles are dispersed is formed. Subsequently, the amorphous titania is changed into crystalline titania by heating the pavement to a temperature of about 700 ° C.
[0012]
(4) Amorphous silica precursor in a solution of amorphous titania precursor (organic titanium compound such as titanium alkoxide, chelate or acetate, or inorganic titanium compound such as TiCl 4 or Ti (SO 4 ) 2 ). (E.g., tetraalkoxysilanes such as tetraethoxysilane, tetraisopropoxysilane, tetra n-propoxysilane, tetrabutoxysilane, tetramethoxysilane, etc .; hydrolyzed silanols thereof; or polysiloxanes having an average molecular weight of 3000 or less ) And then applied by spray coating or dip coating to the surface of the pavement and the inner peripheral surface of the pores near the surface. Subsequently, these precursors are subjected to hydrolysis and dehydration condensation polymerization to form a thin film made of a mixture of amorphous titania and amorphous silica. Subsequently, the amorphous titania is changed into crystalline titania by heating the pavement to a temperature of about 700 ° C.
[0013]
In another embodiment of the present invention, the photocatalyst-containing layer 18 can be formed by dispersing particles of photocatalyst such as anatase titania in a proportion of 50% by weight or less in silicone (organopolysiloxane). Therefore, it is possible to use a coating composition in which titania particles are dispersed in a film-forming element made of uncured or partially cured silicone or a precursor of silicone.
[0014]
Examples of coating film forming elements include methyltrichlorosilane, methyltribromosilane, methyltrimethoxysilane, methyltriethoxysilane, methyltriisopropoxysilane, methyltri-t-butoxysilane; ethyltrichlorosilane, ethyltribromosilane, ethyltrimethoxy Silane, ethyltriethoxysilane, ethyltriisopropoxysilane, ethyltri-t-butoxysilane; n-propyltrichlorosilane, n-propyltribromosilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, n-propyltri Isopropoxysilane, n-propyltri-t-butoxysilane; n-hexyltrichlorosilane, n-hexyltribromosilane, n-hexyltrimethoxysilane, n-hexyltriethoxysilane n-hexyltriisopropoxysilane, n-hexyltri-t-butoxysilane; n-decyltrichlorosilane, n-decyltribromosilane, n-decyltrimethoxysilane, n-decyltriethoxysilane, n-decyltriisopropoxysilane N-decyltri-t-butoxysilane; n-octadecyltrichlorosilane, n-octadecyltribromosilane, n-octadecyltrimethoxysilane, n-octadecyltriethoxysilane, n-octadecyltriisopropoxysilane, n-octadecyltri-t- Butoxysilane; phenyltrichlorosilane, phenyltribromosilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltriisopropoxysilane, phenyltrit-butoxysilane; tetrac Silane, tetrabromosilane, tetramethoxysilane, tetraethoxysilane, tetrabutoxysilane, dimethoxydiethoxysilane; dimethyldichlorosilane, dimethyldibromosilane, dimethyldimethoxysilane, dimethyldiethoxysilane; diphenyldichlorosilane, diphenyldibromo Silane, diphenyldimethoxysilane, diphenyldiethoxysilane; phenylmethyldichlorosilane, phenylmethyldibromosilane, phenylmethyldimethoxysilane, phenylmethyldiethoxysilane; trichlorohydrosilane, tribromohydrosilane, trimethoxyhydrosilane, triethoxyhydrosilane, tri Isopropoxyhydrosilane, tri-t-butoxyhydrosilane; vinyltrichlorosilane, vinyltribromosilane, Vinyltrimethoxysilane, vinyltriethoxysilane, vinyltriisopropoxysilane, vinyltri-t-butoxysilane; trifluoropropyltrichlorosilane, trifluoropropyltribromosilane, trifluoropropyltrimethoxysilane, trifluoropropyltriethoxysilane, tri Fluoropropyltriisopropoxysilane, trifluoropropyltri-t-butoxysilane; γ-glycidoxypropylmethyldimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycyl Sidoxypropyltriethoxysilane, γ-glycidoxypropyltriisopropoxysilane, γ-glycidoxypropyltri-t-butoxysilane; γ-methacryloxypropyl Tildimethoxysilane, γ-methacryloxypropylmethyldiethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropyltriethoxysilane, γ-methacryloxypropyltriisopropoxysilane, γ-methacrylic Roxypropyltri-t-butoxysilane; γ-aminopropylmethyldimethoxysilane, γ-aminopropylmethyldiethoxysilane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-aminopropyltriisopropoxysilane, γ-aminopropyltri-t-butoxysilane; γ-mercaptopropylmethyldimethoxysilane, γ-mercaptopropylmethyldiethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-mercaptopropi Lutriethoxysilane, γ-mercaptopropyltriisopropoxysilane, γ-mercaptopropyltri-t-butoxysilane; β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, β- (3,4-epoxycyclohexyl) ethyltri Ethoxysilanes; partial hydrolysates thereof; and mixtures thereof can be used.
[0015]
This coating composition is applied to the surface of the paving material and the inner peripheral surface of pores near the surface, and the silicone is cured at a temperature of about 100 ° C to 200 ° C. When a pavement such as a sidewalk is constructed using this pavement, the pavement is exposed to the sun during the daytime, and the photocatalyst located near the surface of the pavement is photoexcited by sunlight. Along with the photoexcitation, a silicone derivative in which an organic group bonded to a silicon atom of the silicone molecule is at least partially substituted with a hydroxyl group is formed on the surface of the photocatalyst-containing silicone layer 18 by the action of the photocatalyst. It is superhydrophilic to such an extent that the contact angle becomes about 0 °.
[0016]
Lipophilic contaminants such as carbon black in urban dust are less likely to adhere to the surface of the photocatalyst-containing layer 18 that has been highly hydrophilized. Further, the surface of the superhydrophilic photocatalyst-containing layer 18 absorbs moisture in the air and is not charged by static electricity, so that dust does not easily adhere electrostatically. Furthermore, since the contact angle of inorganic substances such as mud and soil with water is 20 ° to 50 °, the photocatalyst containing layer 18 that has been superhydrophilicized to such an extent that the contact angle with water becomes about 0 ° is included in the photocatalyst containing layer 18. Inorganic dust such as mud and soil is difficult to adhere.
The water affinity of the superhydrophilic surface is greater than the affinity for lipophilic contaminants such as carbon black, so when pavement is exposed to rain, the dirt attached to the inner surface of the pores is The inside of the pores is self-cleaned.
As a result, clogging of the pores is prevented, and the paving material maintains excellent water permeability for a long period of time.
[0017]
In yet another embodiment of the present invention, the pavement is formed by coating aggregate particles 12 with a photocatalyst containing layer 18 in advance, kneading with an inorganic binder such as glass, frit, feldspar, etc. It can be formed by firing at a temperature.
[0018]
【The invention's effect】
According to the present invention, dirt is prevented from adhering to the pores of the water-permeable pavement, and the dirt adhering to the inner peripheral surface of the pores is washed away by rain water every rain, and the pores are self-cleaned. The water permeability of the paving material can be maintained over a long period of time.
[Brief description of the drawings]
FIG. 1 is a schematic enlarged sectional view of a water-permeable pavement material of the present invention.
FIG. 2 is a cross-sectional view in which a part of the pavement shown in FIG. 1 is further enlarged.
[Explanation of symbols]
10: Water-permeable pavement material 16: Pore 18: Photocatalyst containing layer
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16864596A JP3744061B2 (en) | 1995-07-08 | 1996-06-06 | Permeable pavement material |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20501995 | 1995-07-08 | ||
JP7-205019 | 1995-07-08 | ||
JP35464995 | 1995-12-22 | ||
JP7-354649 | 1995-12-22 | ||
JP16864596A JP3744061B2 (en) | 1995-07-08 | 1996-06-06 | Permeable pavement material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH09228307A JPH09228307A (en) | 1997-09-02 |
JP3744061B2 true JP3744061B2 (en) | 2006-02-08 |
Family
ID=27317295
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13653496A Expired - Lifetime JP3972080B2 (en) | 1995-07-08 | 1996-05-30 | Automobile and its painting method |
JP13658796A Expired - Lifetime JP3972081B2 (en) | 1995-07-08 | 1996-05-30 | Railway vehicle and painting method thereof |
JP15920196A Expired - Lifetime JP3661814B2 (en) | 1995-07-08 | 1996-05-31 | Membrane structure material and cleaning method thereof |
JP8160511A Pending JPH09230104A (en) | 1995-07-08 | 1996-05-31 | Lens for eye and its hydrophilic treatment |
JP16864596A Expired - Lifetime JP3744061B2 (en) | 1995-07-08 | 1996-06-06 | Permeable pavement material |
Family Applications Before (4)
Application Number | Title | Priority Date | Filing Date |
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JP13653496A Expired - Lifetime JP3972080B2 (en) | 1995-07-08 | 1996-05-30 | Automobile and its painting method |
JP13658796A Expired - Lifetime JP3972081B2 (en) | 1995-07-08 | 1996-05-30 | Railway vehicle and painting method thereof |
JP15920196A Expired - Lifetime JP3661814B2 (en) | 1995-07-08 | 1996-05-31 | Membrane structure material and cleaning method thereof |
JP8160511A Pending JPH09230104A (en) | 1995-07-08 | 1996-05-31 | Lens for eye and its hydrophilic treatment |
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JP (5) | JP3972080B2 (en) |
Families Citing this family (6)
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JP4894085B2 (en) * | 2001-02-02 | 2012-03-07 | 東レ株式会社 | Surface treatment method for plastic molded product and surface-treated plastic molded product |
DE10123012C1 (en) * | 2001-05-11 | 2002-07-25 | Pharm Pur Gmbh | Passivation of intraoccular lens, especially silicone, polymethyl methacrylate and acrylic intraoccular lens, comprises dipping in solution of fluoroalkyl-hydroxy- and/or -alkoxy-silane to deactivate Bronsted centers on surface |
JP2006507291A (en) | 2002-10-25 | 2006-03-02 | エッセンティア バイオシステムズ インク | Modulating zinc levels to improve tissue properties |
JP2006347364A (en) * | 2005-06-16 | 2006-12-28 | Railway Technical Res Inst | Coating agent for railway rolling stock, its applying method, its manufacturing method, and railway rolling stock |
KR101145321B1 (en) * | 2011-10-14 | 2012-05-14 | 주식회사 폴리그린테크놀로지즈앤드프로덕츠 | Water permeability block |
US20220342122A1 (en) * | 2021-04-22 | 2022-10-27 | Tianchen Innovative Materials Technology Co., Ltd | Optical material, optical product, and manufacturing method thereof |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH07113095B2 (en) * | 1987-05-07 | 1995-12-06 | セイコーエプソン株式会社 | Paint containing titanium oxide |
JPH01218622A (en) * | 1988-02-26 | 1989-08-31 | Agency Of Ind Science & Technol | Method for removing nitrogen oxides in low concentration from air |
JPH0636904B2 (en) * | 1988-11-18 | 1994-05-18 | 大日本塗料株式会社 | Method for forming white coating film with excellent weather resistance |
JP3203413B2 (en) * | 1991-12-20 | 2001-08-27 | 東海旅客鉄道株式会社 | Repair method of railcar skin |
JP2667331B2 (en) * | 1992-03-13 | 1997-10-27 | 東陶機器株式会社 | Member having photocatalytic function and method for manufacturing the same |
JP3230838B2 (en) * | 1992-04-15 | 2001-11-19 | 新日鐵化学株式会社 | Auto bodies and parts |
JP3147251B2 (en) * | 1992-04-28 | 2001-03-19 | セントラル硝子株式会社 | Hydrophilic coating and method for forming the coating |
JP3340149B2 (en) * | 1992-04-28 | 2002-11-05 | セントラル硝子株式会社 | Hydrophilic coating and method for forming the coating |
JPH06190340A (en) * | 1992-09-11 | 1994-07-12 | Sekisui Jushi Co Ltd | Coated metal body |
JPH06278241A (en) * | 1992-09-22 | 1994-10-04 | Takenaka Komuten Co Ltd | Building material |
JP3316048B2 (en) * | 1992-11-06 | 2002-08-19 | 株式会社竹中工務店 | Building material and manufacturing method thereof |
JPH06248545A (en) * | 1993-02-19 | 1994-09-06 | Suzuki Sogyo Co Ltd | Composite material |
JPH06313301A (en) * | 1993-04-30 | 1994-11-08 | Yokohama Rubber Co Ltd:The | Elastic pavement block and manufacture thereof |
JPH0735373A (en) * | 1993-07-22 | 1995-02-07 | Japan Storage Battery Co Ltd | Air-conditioning system |
JPH08117683A (en) * | 1994-10-24 | 1996-05-14 | Sekisui Jushi Co Ltd | Coated body and production of coated body |
BR9607868A (en) * | 1995-03-20 | 1998-06-30 | Toto Ltd | Mirror lens and transparent leaf member with anti-clogging composite with a hydrophilic surface anti-fog process to prevent a mirror, lens or transparent leaf member from becoming cloudy or cloudy with moisture condensate and / or water droplets adhering processes to make the surface of the water hydrophilic a substrate to clean a substrate to keep the surface of a substrate positioned outdoors clean to prevent the growth of adherent water droplets on a substrate and to prepare a mirror a lens and a transparent leaf member with fogging and a self-cleaning compound with a hydrophilic surface and anti-fog glass |
-
1996
- 1996-05-30 JP JP13653496A patent/JP3972080B2/en not_active Expired - Lifetime
- 1996-05-30 JP JP13658796A patent/JP3972081B2/en not_active Expired - Lifetime
- 1996-05-31 JP JP15920196A patent/JP3661814B2/en not_active Expired - Lifetime
- 1996-05-31 JP JP8160511A patent/JPH09230104A/en active Pending
- 1996-06-06 JP JP16864596A patent/JP3744061B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH09225385A (en) | 1997-09-02 |
JP3972081B2 (en) | 2007-09-05 |
JPH09228695A (en) | 1997-09-02 |
JP3972080B2 (en) | 2007-09-05 |
JPH09228307A (en) | 1997-09-02 |
JP3661814B2 (en) | 2005-06-22 |
JPH09225392A (en) | 1997-09-02 |
JPH09230104A (en) | 1997-09-05 |
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