JP2001121643A - Antistaining member - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an antistaining member having sufficient film strength, hard to bond a stain stably over a long period of time and capable of effectively preventing even the propagation of bacteria. SOLUTION: An antistaining member is constituted by forming a layer consisting of an inorganic hydrophilic substance and a hydrophilic substance having photocatalytic function on the surface of a base material or by forming a layer comprising an inorganic hydrophilic substance having photocatalytic function on the surface of the base material.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

TECHNICAL FIELD The present invention relates to a member (including a substrate which can be washed with water) used in an environment having water, that is, a bathtub, a basin, a sink, a toilet, a building material for exterior, and the like. The present invention relates to an antifouling member that can be suitably used as a part.

[0002]

2. Description of the Related Art Metal materials such as stainless steel, plastic materials such as FRP and ABS, and inorganic materials such as enamels, tiles and sanitary ware have been used for members used in an environment with water. I have. In addition, when used in an environment with water, the dirt components are composed of hydrophobic components such as fats and oils, proteins, etc., so that if the substrate surface is hydrophobic, the dirt components are likely to adhere firmly to the surface, Water, it is difficult to remove dirt with water.

[0003] Metal materials such as stainless steel, FRP and ABS
Many plastic materials, such as, are made of hydrophobic substances.
Therefore, in recent years, use of a water-repellent resin has been proposed in order to prevent the dirt component from firmly adhering. In the case of a water-repellent resin, all components are difficult to adhere because of low surface energy. That is, since the dirt component and the water are repelled, the antifouling property is improved.

However, water-repellent resins such as fluororesins are generally soft and easily scratched. Once scratched, stains tended to be formed starting from the scratches, and if the portion was left for a few more days, there was a tendency for the stains to adhere firmly due to propagation of bacteria and the like.

[0005]

On the other hand, when the substrate is used in an environment with water, if the surface of the substrate is hydrophilic, the substrate easily adheres to water and does not easily adhere to dirt. Difficult to adhere to Even if it adheres, it is easy to remove dirt with water.

[0006] However, polyamides and polyvinylidene fluoride, which are generally known hydrophilic polymers, are soft and have a drawback that the film strength is low when the film is formed.

In addition, inorganic vitreous materials such as enamels and glazed tiles generally have hydrophilicity and high film strength. At the time of production, it shows good hydrophilicity with a contact angle to water of about 5 to 20 °. However, in this case, if there is a polar component such as propionic acid in the dirt component, the polar component is gradually adsorbed on the surface, and the surface becomes hydrophobic over time (“Glass Surface Design”, a modern editorial company ( 1983)).

The present invention has been made in view of the above circumstances, and provides an antifouling member having a sufficient film strength, being unlikely to adhere dirt stably for a long period of time, and capable of effectively preventing the propagation of bacteria. With the goal.

[0009]

In order to solve the above problems, the present invention is characterized in that a layer made of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function is formed on the surface of a substrate. Provided is an antifouling member in which a layer made of an inorganic hydrophilic substance having a photocatalytic function is formed on the surface of the antifouling member or the base material. In a preferred embodiment of the present invention, the substance having a photocatalytic function is present in the layer at a thickness of more than 0.3 μm, more preferably at a thickness of 0.6 μm or more.

[0010]

In a member used in an environment with water, a layer composed of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function is formed on the surface of the substrate, or a photocatalytic function is provided on the surface of the substrate. By having a layer made of an inorganic hydrophilic substance having a layer formed, it has sufficient film strength, and it is difficult to stably adhere dirt for a long period of time, so that the propagation of bacteria can be effectively prevented. Become. Further, even if polar components are adsorbed on the surface by irradiating light, they are decomposed by the photocatalytic function and the hydrophilicity of the surface is restored.

Since the base material surface is formed of a hydrophilic substance, hydrophobic dirt components are less likely to adhere to the surface. In addition, due to the presence of a substance having a photocatalytic function on the surface of the base material, even when there is a polar component such as propionic acid in the dirt component, such an adsorbed component is decomposed by the photocatalyst over time, so that the surface Hydrophobicity can be effectively prevented. In addition, propagation of bacteria can be effectively prevented by the action of active oxygen generated by the photocatalyst.

Since the substrate surface is formed of an inorganic material, a layer made of a hydrophilic substance having a sufficient film strength can be realized. When the substance having a photocatalytic function is present in the layer at a thickness exceeding 0.3 μm, the adsorbed component can be sufficiently decomposed.

[0013]

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS A specific embodiment of the present invention will be described below with reference to the drawings. FIG. 1 is a view showing an embodiment of the present invention. A layer made of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function is formed on the surface of a substrate. FIG. 2 is a view showing another embodiment of the present invention, in which a layer made of an inorganic hydrophilic substance having a photocatalytic function is formed on the surface of a substrate.

Here, the material of the substrate may be basically any material such as ceramic, ceramic material, metal, glass, plastic, decorative plywood, calcium silicate, mortar or a composite thereof. The shape of the substrate may be any,
For example, tiles, wall materials, plate-like materials such as floor materials, spherical objects, cylindrical objects, cylindrical objects, rod-like objects, prismatic objects, even simple shapes such as hollow prismatic objects, sanitary ware, Wash basin, bathtub,
It may be of a complicated shape such as a sink and its accessories.

The term "hydrophilic substance" used herein means a substance exhibiting hydrophilicity to such an extent that dirt does not easily adhere thereto, and refers to a substance having a contact angle with water of less than 30 °. This will be specifically described below. FIG. 3 is a diagram in which the relationship between the contact angle with water and the easiness of soiling was examined using various resins. Here, the contact angle to water is measured by a contact angle measuring instrument.
As shown in FIG. 4, the sample was immersed in artificial bath water (warm water obtained by mixing lard and soap discharged by humans) for 3 hours, and the specific gloss near the water level before and after immersion was determined and used as an index for evaluation. . Here, the specific gloss is the gloss after immersion, where the initial gloss before immersion is 1. From FIG. 3, when the contact angle with water is around 70 °, the specific gloss decreases most,
Dirt became easy to adhere. When the contact angle with water became smaller, the specific gloss increased more than when the contact angle was made larger, and hardly changed when the contact angle was less than 30 °.
From the above, it can be said that, when the contact angle with water is less than 30 °, it shows hydrophilicity to such an extent that dirt does not easily adhere.

As the inorganic hydrophilic substance, if it is basically an inorganic oxide, crystalline alumina, partially stabilized zirconia, titanium oxide, zinc oxide, strontium titanate, tungsten trioxide, ferric oxide, dioxide trioxide It may be a crystalline material such as bismuth or tin oxide, or a glass material such as glaze or silicone. Also, inorganic non-oxides can be used as long as they are hydrophilic materials such as silicon nitride and silazane. However, in the case of the embodiment shown in FIG. 1, when an inorganic oxide or an inorganic non-oxide having a property of absorbing ultraviolet light is used, a metal having an electron capturing effect is used to assist a substance having a photocatalytic function. Is desirably added. A plurality of these inorganic hydrophilic substances may be used in combination.

The substance having a photocatalytic function refers to a substance that can generate electrons and holes by irradiation with light having a wavelength equal to or less than a certain wavelength, and thereby generate active oxygen. Among such substances, examples of the substance having hydrophilicity include titanium oxide, zinc oxide, strontium titanate, tungsten trioxide, ferric oxide, bismuth trioxide, and tin oxide. A plurality of these substances having a photocatalytic function may be used in combination.

It is desirable to add a metal having an electron capturing effect to the substance having a photocatalytic function in order to further enhance the photocatalytic function. The metal having an electron trapping effect is P
t, Pd, Au, Ag, Cu, Ni, Fe, Co, Zn
And the like, which have a low ionization tendency and are easily reduced by themselves. These metals may be used in combination.

On the surface of the base material, a layer composed of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function, or a layer composed of an inorganic hydrophilic substance having a photocatalytic function may be formed via a binder layer. . By interposing the binder layer, an antifouling member having more sufficient film strength is obtained. Here, as the binder, both an inorganic binder such as glaze and silicone, and an organic binder such as a thermosetting resin, a photocurable resin, and a thermoplastic resin can be used.

A method for producing the antifouling member shown in FIGS. First, as shown in FIG. 1, regarding a method of producing an antifouling member in which a layer made of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function is formed on the surface of the substrate, the substrate is made of an unglazed tile, The inorganic hydrophilic substance is a glaze, the hydrophilic substance having a photocatalytic function is anatase type titanium oxide,
An example in which copper is added as a substance having an electron capturing effect will be described.

In this case, a step of preparing a mixed solution in which an anatase-type titanium oxide sol suspension and a solution containing copper ions are mixed, a frit-like low-melting glaze is added to the prepared mixed solution, and the mixture is applied by mixing. A step of preparing a liquid, a step of applying a coating liquid on the surface of an unglazed tile base material, and a step of baking are sequentially performed.

Next, a method for producing an antifouling member in which a layer made of an inorganic hydrophilic substance having a photocatalytic function is formed on the surface of the substrate shown in FIG. The case where the conductive substance is anatase-type titanium oxide and copper is added thereto as a substance having an electron trapping effect will be described as an example.

In this case, a step of preparing a coating solution for mixing the anatase type titanium oxide sol suspension and a solution containing copper ions, a step of applying the coating solution to the surface of the glazed tile base material,
There is a method of sequentially performing the firing step. As another method, a method of sequentially applying a step of applying an anatase type titanium oxide sol suspension to the surface of a glazed tile substrate, a step of baking, a step of applying a solution containing copper ions, and a step of irradiating light containing ultraviolet rays is performed. There is.

Here, it is desirable that the anatase type titanium oxide sol is sufficiently dispersed in the suspension. For this purpose, since the isoelectric point of anatase type titanium oxide is pH 6.5, it is dispersed in an acidic or alkaline state. At this time, a surfactant, a dispersant (peptizer) or a surface treating agent may be added to improve dispersibility. As a solvent for dispersing the anatase-type titanium oxide sol, water or ethanol is preferable because it has no toxicity.

As the solution containing copper ions, a solution of a soluble copper compound such as cupric acetate or cupric sulfate can be suitably used. In the case of a metal having an electron capturing effect other than copper, a soluble solution of silver nitrate, silver sulfate, silver lactate, silver acetate or the like is preferable because the mixing treatment is simple. As a solvent used for the solution containing copper ions, water, ethanol, propanol or the like can be used, but it is preferable to use the same type as the anatase type titanium oxide sol suspension as much as possible.

In the step of mixing the copper ion-containing solution with the anatase-type titanium oxide sol suspension, the pH of the copper ion-containing solution is preferably adjusted to be substantially equal to the pH of the anatase-type titanium oxide sol suspension. This is because the change in the pH of the anatase-type titanium oxide sol suspension is small, and the dispersibility of the anatase-type titanium oxide sol in the suspension is not significantly impaired.

After mixing a solution containing copper ions with the anatase type titanium oxide sol suspension, the solution may be irradiated with light containing ultraviolet rays. In this case, since copper can be fixed to the anatase-type titanium oxide particles by photoreduction, the photocatalytic function can be improved.

The light containing ultraviolet light is light having energy sufficient to reduce metal ions having an electron capturing effect such as copper ions. The method of applying the coating liquid to the substrate may be basically any method. For example,
Spray coating method, roll coating method,
Dip coating can be used.

The effects of the above embodiment will be described below based on specific evaluation experiments. (Evaluation experiment 1) Ammonia-peptized anatase-type titanium oxide sol suspension having an average particle size of 0.01 μm is applied to the surface of a glazed tile substrate of 15 cm square by a spray coating method, and baked at 880 ° C. An anatase-type titanium oxide layer was formed. Thereafter, an aqueous solution containing 5% by weight of copper acetate was applied thereto, and irradiated with light including ultraviolet rays by a BLB lamp to obtain a sample having a 0.9 μm-thick anatase-type titanium oxide layer. This sample was evaluated for the contact angle with water, the recovery of the contact angle with water by light irradiation, the ease with which dirt adheres, the antibacterial properties, and the abrasion resistance.

As shown in FIG. 4, the degree of adhesion of dirt is determined by immersing the sample in artificial bath water (warm water obtained by mixing red, lard, and soap discharged by a human) for 3 hours, and near the water level before and after the immersion. Was determined and used as an index for evaluation (a small specific gloss indicates that the sample is easily stained).

The recovery of the contact angle to water by light irradiation was evaluated by the recovery of the contact angle to water after irradiating the sample exposed to a polar component (such as carboxylic acid) for 1 week in a dark place with a BLB lamp for 5 days. did.

The antibacterial activity is determined by Escherichia coli (Escherichia).
a coli W3110 strain). 7 in advance
A bacterial solution of 0.1% was added to the outermost surface of the sample sterilized with 0% ethanol.
A glass plate (100 × 100) onto which 5 ml (10,000 to 50,000 CFU) was dropped was brought into close contact with a white light (350
(0 lux) for 30 minutes, and the bacterial solution was wiped with sterile gauze and collected in 10 ml of physiological saline, and the survival rate of the bacteria was determined and used as an index for evaluation. The evaluation index is shown below. +++: Escherichia coli survival rate of less than 10% ++: Escherichia coli survival rate of 10% or more and less than 30% +: Escherichia coli survival rate of 30%
More than 70%-: Escherichia coli survival rate 70% or more

In the abrasion resistance test, sliding abrasion using a plastic eraser was performed, and changes in appearance were compared and evaluated. The evaluation criteria are shown below. ◎: No change after reciprocation 40 times ○: Scratched by sliding 10 times or more and less than 40 times, peeling off hydrophilic film △: 5 times or more 1
Scratching occurs less than 0 times and the hydrophilic film peels off. X: Scratching occurs less than 5 times and the hydrophilic film peels off.

As a result, the contact angle with water was 9 °, indicating a sufficient hydrophilicity, and the change in glossiness was scarcely observed at 0.95 with respect to the ease with which dirt adhered. In addition, the recovery of the contact angle with respect to water by light irradiation increased to 30 ° when left in a dark place, but recovered to 7 °. For comparison, a similar test was performed on the sheet glass, but it was 40 ° when left in a dark place, but it did not recover to a hydrophilic state of 50 ° even when irradiated with light.
In addition, the antibacterial properties of the working samples were +++, and the abrasion resistance was ◎, indicating good results.

(Evaluation Experiment 2) An ammonia-peptized anatase-type titanium oxide sol suspension having an average particle size of 0.01 μm was
A 15 cm square glazed tile base material was applied by a spray coating method and baked at 880 ° C. to form a hydrophilic anatase-type titanium oxide layer. Then 5% by weight
A copper acetate aqueous solution was applied, and light including ultraviolet rays was irradiated by a BLB lamp to obtain samples having anatase-type titanium oxide layers of various thicknesses. This sample was placed on the floor of a public bath in an employee dormitory, which is expected to be exposed to all of the bacteria, hydrophobic dirt components and polar dirt components.
Exposure for about a day. In this test, the floor of the public bath was properly cleaned by a cleaning staff.

As shown in FIG. 5, as shown in FIG. 5, when the thickness of the anatase type titanium oxide layer was 0.3 μm, no great effect was obtained as compared with the glazed tile, but the thickness was 0.6 μm, 0.9 μm
It was found that the glossiness showed almost no change from the initial value even after 100 days had passed, indicating excellent antifouling properties.

[0037]

As described above, in a member used in an environment where water is present, a layer made of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function is formed on the surface of the substrate, or a photocatalyst is formed on the surface of the substrate. By forming a layer composed of an inorganic hydrophilic substance having a function, it has sufficient film strength, and it is difficult to stably adhere dirt over a long period of time, effectively preventing the propagation of bacteria. Will be able to gain.

[Brief description of the drawings]

FIG. 1 is a diagram showing one embodiment of the present invention.

FIG. 2 is a diagram showing another embodiment of the present invention.

FIG. 3 is a diagram showing a relationship between a contact angle with water and the easiness of soiling.

FIG. 4 is a diagram showing an antifouling evaluation device.

FIG. 5 is a view showing a specific glossiness in a public bath exposure test.

[Explanation of symbols]

 DESCRIPTION OF SYMBOLS 1 Substrate 2 Inorganic hydrophilic substance which has a photocatalytic function 3 Inorganic hydrophilic substance 4 Dirt 5 Artificial bath water 6 Sample

──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. ⁷ Identification symbol FI Theme coat ゛ (Reference) A47K 3/02 A47K 3/02 C08J 7/06 CER C08J 7/06 CERZ CEZ CEZZ C09K 3/18 C09K 3 / 18 // C08L 101: 00 C08L 101: 00 (72) Inventor Shin Hayakawa 2-1-1 Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka Touchi Kiki Co., Ltd. (72) Inventor Toshiya Watanabe Kokura, Kitakyushu-shi, Fukuoka 2-1-1 Nakajima, Kita-ku Toto Kiki Co., Ltd.

Claims (3)

[Claims] 1. An antifouling member characterized in that a layer made of an inorganic hydrophilic substance and a hydrophilic substance having a photocatalytic function is formed on the surface of a substrate. 2. An antifouling member characterized in that a layer made of an inorganic hydrophilic substance having a photocatalytic function is formed on the surface of a substrate. 3. The antifouling member according to claim 1, wherein the substance having a photocatalytic function is present in the layer in a thickness exceeding 0.3 μm.