JP2011063852A - Product with soil resistant finish and manufacturing method therefor - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a product with a soil resistant finish, which has a soil-resistant coating film that is superior in a scorch prevention effect, can maintain the scorch prevention effect for a long period and can make the adhering scorch easily removed, and to provide a manufacturing method therefor. <P>SOLUTION: The product with the soil resistant finish includes a metal substrate and the soil-resistant coating film formed on the surface of the metal substrate. The soil-resistant coating film is formed by sequentially stacking: the first layer containing zirconium oxide; the second layer which is formed on the first layer and contains an alkali silicate; and the third layer which is formed on the second layer and contains at least one oxide selected from zirconium oxide, yttrium oxide, hafnium oxide and an oxide of a rare earth element. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to an antifouling processed product and a method for producing the same, and in particular, an antifouling process that is excellent in sustainability of the non-burning effect and the non-burning effect, and can be easily removed even when the burnt sticks to the surface of the product substrate. The present invention relates to a product and a manufacturing method thereof.

  A hydrophilic coating process has been effective as a method for improving the cleaning performance of dirt such as stainless steel. For example, Patent Document 1 discloses a method for forming a hydrophilic film in which a coating for forming a hydrophilic film containing a silicon component, a zirconium component and water is applied to a base material and cured by a hydration reaction to form a film. It is described that when an aqueous solution containing silicate ions or the like is applied to this film, the hydration reaction is further accelerated and the curing is accelerated.

  Moreover, a non-stick coating film was formed on the inner wall of the oven used at high temperature. As the non-burning coating film, for example, a fluorine-based or silicone-based water-repellent resin film is used, and further, enamel processing is employed when it is necessary to cope with high temperatures and scratches.

International Publication No. 03/080744 Pamphlet

However, the non-stick coating film according to the background art has the following problems.
For example, if the inner wall of the oven is made of stainless steel, the heat efficiency of the oven is improved by heat reflection due to the metallic luster. However, in the case of pure stainless steel, there are problems of loss of aesthetics due to the generation of temper color due to heat, and it is difficult to remove when food burns.

In the hydrophilic coating process disclosed in Patent Document 1, when the outermost layer is a layer containing silicate ions, the silicate ions are burnt when used on a portion where the burns occur, such as the inner wall of an oven. There was a problem that it was not possible to remove the burnt.
Further, when a water-repellent resin is applied to the oven inner wall, heat reflection due to the metallic luster of stainless steel is hindered. Furthermore, the water-repellent resin itself is easily damaged and has a problem that it cannot withstand high temperatures of 300 ° C. or higher.
On the other hand, in the case of enamel treatment, there is no problem in heat resistance and resistance to scratching, but there is a problem that scorching is difficult to remove and heat reflection due to the metallic luster of stainless steel is hindered.
As described above, there has not yet been a method of preventing the heat reflection of stainless steel from being damaged, being hard to be damaged, suppressing the generation of the temper color, and making the heated object such as food difficult to burn.

  The present invention has been made in view of the problems of the background art described above, and is excellent in anti-burning effect, has long-lasting anti-burning effect, and can easily remove the attached burning. An object of the present invention is to provide an antifouling processed product having a coating film and a manufacturing method thereof.

  In order to solve the above problems, an antifouling processed product of the present invention includes a metal substrate and an antifouling coating film formed on the surface of the metal substrate, and the antifouling coating film is formed on the metal substrate. A first layer containing zirconium oxide, a second layer formed on the first layer and containing an alkali silicate, and a zirconium oxide, yttrium oxide formed on the second layer, And a third layer containing at least one selected from hafnium oxide and rare earth oxide.

  The third layer preferably contains 70% by mass or more of at least one selected from zirconium oxide, yttrium oxide, hafnium oxide, and rare earth oxide.

  The first layer preferably contains 30% by mass or more of zirconium oxide.

  The method for producing an antifouling processed product of the present invention comprises a zirconium-containing component comprising at least one selected from zirconia sol, zirconium alkoxide, a partial hydrolysis product of the zirconium alkoxide, and a zirconium salt on the surface of a metal substrate. And applying a heat treatment to form a first layer made of the heat treatment product, applying a coating solution containing an alkali silicate on the first layer, applying a heat treatment, A step of forming a second layer comprising the heat treatment product, and a sol, alkoxide and partial hydrolysis product of at least one component selected from zirconium, yttrium, hafnium and rare earth elements on the second layer And a coating solution containing at least one selected from salts, heat-treated, and the heat-treated product. Forming a third layer, and having a.

The antifouling processed product of the present invention has an excellent anti-burning effect, the excellent anti-burning effect lasts for a long period of time, and can be easily removed with a simple operation. For this reason, no strong chemicals or abrasives are required to remove the fixed scorch, which has the effect of reducing labor and reducing the burden on the environment.
Furthermore, when the antifouling processed product of the present invention is used in an oven or the like, the heat efficiency of the oven or the like can be improved without impairing the reflection of a metal substrate such as stainless steel, and the occurrence of temper color is suppressed, It has the effect of not detracting from aesthetics.
Moreover, the manufacturing method of the antifouling processed product of this invention can manufacture the antifouling processed product which shows said effect simply and efficiently.

The figure which shows the cross-section of the antifouling | stain-resistant processed product which concerns on embodiment.

  Hereinafter, embodiments of the present invention will be described.

"Anti-fouling processed products"
First, an embodiment of the antifouling processed product will be described.
FIG. 1 is a diagram showing a cross-sectional structure of an antifouling processed product 10 according to an embodiment of the present invention.
As shown in FIG. 1, the antifouling processed product 10 of this embodiment is characterized by a first layer 21 formed on the surface of a metal product substrate (metal substrate) 11 and on the first layer 21. The antifouling coating film 20 having a three-layer structure including the formed second layer 22 and the third layer 23 formed on the second layer 22 is provided.

More specifically, the first layer 21 is made of a film forming material containing a zirconium oxide component, the second layer 22 is made of a film forming material containing an alkali silicate, and the third layer 23 is made of zirconium oxide or yttrium. It is made of a film forming material containing at least one component selected from oxides, hafnium oxides and rare earth oxides.
Further, the metal product base 11 is not particularly limited, and includes metal products such as stainless steel, aluminum, plated steel plate, and titanium. Further, the shape of the product substrate 11 is not particularly limited, and may be a bulk-shaped molded body, or may be a plate shape or a linear shape.

The film | membrane containing the zirconium oxide component which comprises the 1st layer 21 should just contain the zirconium oxide component. The content of zirconium oxide in the film of the first layer 21 is preferably 30% by mass or more. When the zirconium oxide content is less than 30% by mass, the durability may be reduced by steam during cooking.
The components other than zirconium oxide contained in the first layer 21 are not particularly limited, but silica (silicon oxide) is preferable.

The second layer 22 is a film containing an alkali silicate. The content of alkali silicate in the film of the second layer 22 is preferably 60% by mass or more and 95% by mass or less in terms of silicon dioxide (SiO ₂ ) as a silicon component. More preferably, it is the range of 70 mass% or more and 95 mass% or less. When the content of the silicon component is less than 60% by mass in terms of silicon dioxide, the second layer 22 may be dissolved by water vapor, and when it exceeds 95% by mass, the film may be easily cracked.

  The content of the alkali component is preferably 5% by mass or more and 40% by mass or less in terms of oxide. More preferably, it is the range of 10 mass% or more and 25 mass% or less. When the content of the alkali component is less than 5% by mass in terms of oxide, the film may be easily cracked, and when it exceeds 40% by mass, it may be dissolved by water vapor.

  As the alkali component, lithium, sodium, potassium, rubidium, cesium, francium alkali metal components are used. Of these, sodium and lithium are preferable, and sodium and lithium are preferably used in combination.

When sodium and lithium are contained as the alkali components, the alkali silicate in the film of the second layer 22 has a silicon component of 70% by mass to 95% by mass in terms of SiO ₂ and a sodium component in terms of Na ₂ O. In the range of 4.5 mass% to 20 mass%, the lithium component is preferably in the range of 0.5 mass% to 10 mass% in terms of Li ₂ O. In addition, the content of the alkali component obtained by adding the sodium component and the lithium component in the above range is preferably 5% by mass or more and 30% by mass or less in terms of oxide.

Silicon component is less than 70 wt% in terms of SiO _2, insufficient steam resistance of the coating, is deteriorated coating property exceeds 95 mass%.
When the sodium component exceeds 20% by mass in terms of Na ₂ O, the alkali resistance and acid resistance of the coating are insufficient, and when it is less than 2% by mass, the paintability deteriorates.
When the lithium component exceeds 10% in terms of Li ₂ O, the alkali resistance of the coating deteriorates, and when it is less than 0.5%, the acid resistance of the coating deteriorates.

  The third layer 23 includes at least one metal oxide selected from zirconium oxide, yttrium oxide, hafnium oxide, and rare earth oxide. The total of these metal oxide components in the film of the third layer 23 is preferably 70% by mass or more. When the content of these components is less than 70% by mass, sufficient anti-burning effect cannot be obtained in the antifouling coating film 20, and the heat reflectivity of the antifouling processed product 10 tends to decrease.

When the composition includes two or more metal oxides selected from zirconium oxide, yttrium oxide, hafnium oxide, and rare earth oxide, the composition preferably includes zirconium oxide. In this case, the content ratio of zirconium oxide and other oxides (yttrium oxide, hafnium oxide, and rare earth oxide) is 30% by mass to 100% by mass of zirconium oxide in the total of these metal oxides. It is preferable to contain in the range below%. If the zirconium oxide content is less than 30% by mass, the strength of the film may be weakened.
Although there is no particular limitation on components other than these metal oxides, the third layer 23 preferably has a composition that does not contain silica (silicon oxide).

The role of each layer is as follows.
First, the outermost third layer 23 will be described. The role of the third layer 23 is to prevent the food from being burnt and to prevent the reflection from decreasing. Here, when the silica component is contained in the third layer 23, the food is easily burnt. Therefore, it is necessary to reduce the content of the silica component in the third layer 23 as much as possible, and the coating does not substantially contain silica. It is preferable that Suitable materials for the third layer 23 are zirconium oxide, yttrium oxide, hafnium oxide, and rare earth oxide as described above. These components are not only difficult to burn, but also have a higher refractive index than silica, so that they easily reflect light rays, and can be an antifouling processed product that can be suitably used as an inner wall material of an oven.

  Next, the role of the second layer 22 is to prevent the product base 11 made of stainless steel or the like from being damaged and to prevent the generation of a temper color. The oxide layer containing alkali silicate is hard and has the effect of preventing the generation of temper color. However, since it is easy to burn, the antifouling coating film 20 of the present embodiment covers the second layer 22 with the third layer 23.

  Next, the role of the first layer 21 is to improve the adhesion of the coating. When the first layer 21 is not formed, sufficient adhesion between the antifouling coating film 20 and the product substrate 11 cannot be obtained. For example, when exposed to water vapor for a long time, the antifouling coating film 20 is formed on the product substrate 11. It peels off from the surface. In addition, since the antifouling coating film 20 composed only of the first layer 21 cannot provide a sufficient damage prevention effect and temper color prevention effect, it is necessary to provide the second layer 22.

The thickness of each layer in the antifouling coating film 20 is preferably 20 nm to 200 nm, the second layer 22 is 100 nm to 1000 nm, and the third layer 23 is 20 nm to 200 nm.
When the first layer 21 is less than 20 nm, sufficient adhesion cannot be obtained, and when it exceeds 200 nm, cracks are likely to occur. Further, if the second layer 22 is less than 100 nm, sufficient damage prevention effect and temper color prevention effect cannot be obtained, and if it exceeds 1000 nm, cracks are likely to occur. Further, if the third layer 23 is less than 20 nm, the desired effect of preventing burning cannot be obtained, and if it exceeds 200 nm, cracks tend to occur. When cracks occur in the antifouling coating film 20, the transparency of the coating is impaired, and the heat reflectivity is also impaired.

"Production method of antifouling processed products"
Next, an embodiment of the method for producing an antifouling processed product of the present invention will be described.
The method for producing an antifouling processed product of the present embodiment comprises at least one zirconium selected from zirconia sol, zirconium alkoxide and its partial hydrolysis product, and zirconium salt on the surface of the product substrate 11 (metal substrate). A step of applying a coating solution containing a component, heat-treating the coating solution, and forming a first layer 21 made of the heat-treated product;
Next, a step of applying a coating solution containing an alkali silicate on the first layer 21 and performing a heat treatment to form a second layer 22 made of the heat treatment product,
Furthermore, on the second layer 22, a coating containing at least one selected from a sol of at least one component selected from zirconium, yttrium, hafnium and a rare earth element, an alkoxide and a partial hydrolysis product thereof, and a salt. And applying a liquid and heat-treating it to form a third layer 23 made of the heat-treated product.

  The zirconium sol contained in the coating solution for forming the first layer 21 is not particularly limited, but it is preferable from the viewpoint of sinterability to use zirconia fine particles having a particle diameter of 5 nm or less. For example, a zirconia sol “nanozirconia dispersion liquid” manufactured by Sumitomo Osaka Cement Co., Ltd. can be suitably used.

  Further, as the zirconium alkoxide, a hydrolyzate or a chelate compound thereof can also be used. Although it does not restrict | limit especially as said zirconium alkoxide, For example, a zirconium tetranormal butoxide and a zirconium tetrapropoxide can be illustrated. These zirconium tetranormal butoxide and zirconium tetrapropoxide have an appropriate hydrolysis rate and are easy to handle, so that a thin film having a uniform film quality can be formed.

  Furthermore, the hydrolyzate of zirconium alkoxide is not particularly limited, and examples thereof include a hydrolyzate of zirconium tetranormal butoxide and a hydrolyzate of zirconium tetrapropoxide. There is no restriction | limiting in particular as a hydrolysis rate of this hydrolyzate, The thing in the range of more than 0 mol%-100 mol% can be used.

By the way, these zirconium alkoxides and hydrolysates of zirconium alkoxides are highly hygroscopic and unstable, and are not sufficiently stable in storage.
Therefore, from the viewpoint of ease of handling, zirconium alkoxide chelate compounds obtained by chelating these zirconium alkoxides and zirconium alkoxide hydrolysates and zirconium alkoxide hydrolyzate chelate compounds are preferred.

As a chelate compound of zirconium alkoxide, zirconium alkoxide, ethanolamine such as monoethanolamine, diethanolamine and triethanolamine, β-diketone such as acetylacetone, methyl acetoacetate, ethyl acetoacetate, diethyl malonate, ethyl phenoxyacetate and the like Examples of reaction products with one or more hydrolysis inhibitors (compounds) selected from the group of carboxylic acids such as β-keto acid esters, acetic acid, lactic acid, citric acid, benzoic acid and malic acid be able to.
Here, the hydrolysis inhibitor is a compound having an action of forming a chelate compound with zirconium alkoxide and suppressing the hydrolysis reaction of the chelate compound.

  Further, as a chelate compound of a hydrolyzate of zirconium alkoxide, a hydrolyzate of zirconium alkoxide, ethanolamine such as monoethanolamine, diethanolamine, and triethanolamine, β-diketone such as acetylacetone, methyl acetoacetate, ethyl acetoacetate , One or more hydrolysis inhibitors selected from the group of β-keto acid esters such as diethyl malonate and ethyl phenoxyacetate, and carboxylic acids such as acetic acid, lactic acid, citric acid, benzoic acid and malic acid ( The reaction product with a compound) can be illustrated. The definition of the hydrolysis inhibitor is as described above.

  The ratio of the hydrolysis inhibitor to zirconium alkoxide or the hydrolyzate of zirconium alkoxide is preferably 0.5 mol times or more and 4 mol times or less of zirconium (Zr) contained in the zirconium alkoxide or the hydrolyzate of zirconium alkoxide. More preferably, it is the range of 1 mol times or more and 3 mol times or less.

  When the ratio of the hydrolysis inhibitor to the amount of zirconium is less than 0.5 mol times, the stability of the coating solution becomes insufficient. On the other hand, when the said ratio of a hydrolysis inhibitor exceeds 4 mol times, even after heat processing, a hydrolysis inhibitor remains in a thin film, As a result, the hardness of a thin film will fall.

  These zirconium alkoxide chelate compounds and zirconium alkoxide hydrolyzate chelate compounds are obtained by dissolving a zirconium alkoxide or a zirconium alkoxide hydrolyzate in a solvent, and further adding a hydrolysis inhibitor. Thus, a chelation reaction may be caused.

Furthermore, nitrates, chlorides, acetates, and the like can be used as zirconium salts that can form the coating solution used for forming the first layer 21.
An organic solvent or water can be used as the solvent of the coating solution containing these, and alcohols, ketones, esters, and the like can be used as the organic solvent.
The coating solution is preferably adjusted in the range of 1% or more and 20% or less of the solid content according to the coating method.

The alkali silicate contained in the coating solution for forming the second layer 22 is not particularly limited, and an alkali silicate containing an alkali metal can be used. Among these, it is preferable to use sodium silicate and lithium silicate, and it is preferable to use a coating solution containing both sodium silicate and lithium silicate.
As a solvent, water is preferable, and it is preferable to adjust in the range of solid content 1% or more and 20% or less according to the coating method.

As the coating solution for forming the third layer 23, the same one as that used for the coating solution for forming the first layer 21 can be used for zirconium.
As for yttrium, hafnium and rare earth elements, those obtained by replacing zirconium with these components in the above can be used.
An organic solvent or water can be used as the solvent of the coating solution containing these, and alcohols, ketones, esters, and the like can be used as the organic solvent.
The coating solution is preferably adjusted in the range of 1% or more and 20% or less of the solid content according to the coating method.

Hereinafter, the manufacturing procedure of the antifouling processed product of this embodiment will be described in more detail.
First, the first layer forming coating solution is applied to the surface of the product substrate 11 (metal substrate). As a coating method, a known spray method, dipping method, roll method or the like can be applied, and there is no particular limitation.
Thereafter, the coating film is dried and heat-treated. The heat treatment temperature needs to be equal to or lower than the temper color generation temperature of the stainless steel constituting the product substrate 11. The temper color of stainless steel generally starts to be generated in the range of 200 ° C. to 250 ° C., and changes depending on the composition of stainless steel, surface treatment conditions, atmosphere, and time. Therefore, it is necessary to confirm the temper color generation temperature in advance by a preliminary experiment. When the temper color is generated, the corrosion resistance of the temper color itself (oxidized portion of the surface) is small, so that the corrosion resistance of the stainless steel (product base 11) is not improved even if the antifouling coating is applied. For this reason, firing of the first layer 21 must be performed at a temperature at which no temper color is generated.

Next, a second layer forming coating solution is applied to the surface of the first layer 21. The application method is the same as the step of forming the first layer 21.
And said coating film is dried and heat-processed. The heat treatment temperature is preferably set to be equal to or higher than the temper color generation temperature of the stainless steel constituting the product base 11 for the second layer 22. That is, the temperature is preferably 250 ° C. or higher. In the heat treatment of the second layer 22 after the heat treatment of the first layer 21, the surface of the product substrate 11 is covered with the first layer 21, and contact with air on the surface is already cut off, so that the surface is heated to a high temperature. Even so, temper color does not occur. For this reason, it is preferable that the coating layer composed of the first layer 21 and the second layer 22 is firmly baked at a high temperature of 250 ° C. or more to improve the corrosion resistance.

Next, a third layer forming coating solution is applied to the surface of the second layer 22. The application method is the same as the step of forming the first layer 21.
And said coating film is dried and heat-processed. The heat treatment temperature is preferably 250 ° C. or higher for the third layer 23. At the time of heat treatment of the third layer 23, temper color no longer occurs, so it is preferable to perform the heat treatment under conditions as high as possible.

  Next, the present invention will be described in detail with reference to examples and comparative examples.

Example 1
First, 30 parts by weight of zirconium tetrabutoxide, 15 parts by weight of ethyl acetoacetate and 55 parts by weight of 2-propanol were mixed at 25 ° C. for 30 minutes to form a chelate compound of zirconium tetrabutoxide and ethyl acetoacetate, and the first layer was formed. A coating solution was prepared. The solid content of this coating solution was 10%.

Next, sodium silicate, lithium silicate and water are mixed, and the second layer of SiO ₂ : 22%, Na ₂ O: 4%, Li ₂ O: 1%, H ₂ O: 73% in terms of oxides. A coating solution for forming was prepared.
Moreover, the same coating liquid as the coating liquid for 1st layer formation was prepared as a coating liquid for 3rd layer formation.
Further, stainless steel (temper color generating condition of 230 ° C. or higher) was prepared as a metal substrate.

After preparing the above coating solution and substrate, the first layer forming coating solution is applied to the surface of the stainless steel using a roll coater, heat-treated at 220 ° C. for 10 minutes, and then cooled. One layer was formed.
Next, a coating liquid for forming a second layer was applied onto the first layer by a roll coater, heat-treated at 250 ° C. for 10 minutes, and then cooled to form a second layer.
Further, the third layer forming coating solution was applied onto the second layer in the same manner as the first layer, heat-treated at 250 ° C. for 10 minutes, and then cooled to form the third layer. Here, the thickness of the first layer and the third layer was 100 nm, and the thickness of the second layer was 300 nm.
In this way, a three-layer antifouling coating film was formed on the surface of the stainless steel, and the antifouling processed product of the present invention of Example 1 was produced.

(Example 2)
In Example 2, 30 parts by weight of zirconium tetrabutoxide, 15 parts by weight of ethyl acetoacetate, 9 parts by weight of tetramethoxysilane and 46 parts by weight of 2-propanol were mixed at 25 ° C. for 30 minutes, and zirconium tetrabutoxide, tetramethoxysilane and acetoacetate were mixed. A chelate compound with ethyl acetate was formed to prepare a coating solution for forming the third layer. The coating solution had a solid content of 13%, and the ratio of zirconium to silicon was 10: 3 (zirconia 77%) in terms of zirconium dioxide and silicon dioxide.
The coating solution for forming the first layer and the coating solution for forming the second layer were the same as in Example 1.
And each coating liquid was apply | coated to stainless steel on the conditions similar to Example 1, and the antifouling processed product of this invention of Example 2 was produced.

(Example 3)
In Example 3, 30 parts by weight of zirconium tetrabutoxide, 15 parts by weight of ethyl acetoacetate, 15 parts by weight of tetramethoxysilane, and 40 parts by weight of 2-propanol were mixed at 25 ° C. for 30 minutes, and zirconium tetrabutoxide, tetramethoxysilane, and acetoacetate were mixed. A chelate compound with ethyl acetate was formed to prepare a coating solution for forming the third layer. The solid content of this coating solution was 15%, and the ratio of zirconia and silica was 10: 5 (zirconia 67%).
The coating solution for forming the first layer and the coating solution for forming the second layer were the same as in Example 1.
And each coating liquid was apply | coated to stainless steel on the conditions similar to Example 1, and the antifouling processed product of this invention of Example 3 was produced.

(Comparative Example 1)
In Example 1, the first layer was not applied as Comparative Example 1.

(Comparative Example 2)
In Example 1, the second layer was not applied as Comparative Example 2.

(Comparative Example 3)
In Example 1, the third layer was not applied as Comparative Example 3.

  The samples shown in Examples 1, 2, 3 and Comparative Examples 1, 2, 3 were evaluated as follows. Further, the same evaluation was performed on solid stainless steel that does not form an antifouling coating film.

-Citric acid resistance: Each sample was immersed in a citric acid saturated aqueous solution for 24 hours, and then the surface state of the antifouling coating film was evaluated by visually observing the surface.
-Alkali resistance: Each sample was immersed in 5% sodium hydroxide aqueous solution for 24 hours, and then the surface state of the antifouling coating film was evaluated by visual observation of the surface.
Vapor resistance: Each sample was exposed to water vapor at 100 ° C. for 24 hours, and then the surface was visually observed to evaluate changes in the surface state of the antifouling coating film.
Pencil 9H scratch: Performed according to JIS-K5600.
-Soy sauce burn-off: 10 mL of soy sauce was attached to the surface of the antifouling coating film of each sample, heated in air at 250 ° C. for 1 hour, and then exposed to 100 ° C. water vapor for 20 minutes to burn the soy sauce. . Thereafter, the burnt dirt was wiped with a cloth soaked in water, and the ease of removal was evaluated.
Temper color: Each sample was heated in air at 300 ° C. for 1 hour, and then the surface was observed to evaluate the temper color generation state.

As shown in Table 1, the antifouling processed product according to the present invention in which a three-layer antifouling coating film is formed on the surface of stainless steel has acid resistance, alkali resistance, steam resistance, scratch resistance, and easy scoring removal. In addition, good results were shown for any of the temper color suppression effects.
In particular, the samples of Examples 1 and 2 in which the ratio of zirconia in the third layer is 70% or more may be an antifouling processed product suitable as an inner wall material of an oven without causing abnormality in all evaluation items. It could be confirmed.

Example 4
In Example 4, a “nanozirconia aqueous dispersion” particle size 3 nm manufactured by Sumitomo Osaka Cement Co., Ltd. was diluted with water to adjust the solid content to 2%, and a coating solution for forming the first layer was prepared.
Moreover, sodium silicate, lithium silicate, and water are mixed, and the oxide equivalent value is SiO ₂ : 5%, Na ₂ O: 1%, Li ₂ O: 0.1%, H ₂ O: 93.9%. A coating solution for forming the second layer was prepared.
Further, 15 parts by weight of one selected from hafnium tetrabutoxide, yttrium tetrabutoxide, lanthanum butoxide, and cerium tetrabutoxide, 15 parts by weight of zirconium isopropoxide, 15 parts by weight of ethyl acetoacetate, 55 parts by weight of 2-propanol Were mixed at 25 ° C. for 30 minutes to form a chelate compound of each component and ethyl acetoacetate to prepare a coating solution for forming the third layer. The solid content of this coating solution was 10%.

Next, coating treatment was performed on stainless steel (metal substrate) by spray coating using the above-described coating liquids for forming the first to third layers (four kinds of coating liquids for forming the third layer).
That is, as the sample of Example 4, four types of samples were prepared: a sample containing hafnium in the third layer, a sample containing yttrium, a sample containing lanthanum, and a sample containing cerium.

In the coating process, the coating film was heat treated at 220 ° C. for 30 minutes in the first layer forming step, and the coating film was heat treated at 250 ° C. for 30 minutes in the second layer and third layer forming steps.
In addition, the thickness of the antifouling coating film in this example was 50 nm for the first layer, 800 nm for the second layer, and 100 nm for the third layer.

(Example 5)
In Example 5, a mixed liquid of a nano zirconia aqueous dispersion and a colloidal silica dispersion was used as the first layer forming coating liquid. The solid content in the coating solution was 2%, the ratio of zirconia in the solid content was 35%, and the ratio of silica was 65%.
The coating solution for forming the first layer and the coating solution for forming the second layer were the same as in Example 4.
And each coating liquid was apply | coated with respect to stainless steel on the conditions similar to Example 4, and the antifouling processed product of this invention of Example 5 was produced.

(Example 6)
In Example 5, except that the ratio of zirconia in the solid content in the coating liquid for forming the first layer was 25% and the ratio of silica was 75%, the same conditions as in Example 5 were used, and each coating liquid was Stainless steel was sequentially coated to prepare an antifouling processed product of Example 4.

  About each sample of Example 4, 5, and 6, the same evaluation as previous Examples 1-3 was performed.

  As shown in Table 2, the antifouling coating film formed with the third layer containing oxides of rare earth elements such as hafnia, yttria, lanthanum, and cerium in addition to zirconia had good scoring property. Moreover, it was confirmed from the comparison of Examples 5 and 6 that even better alkali resistance and water vapor resistance can be obtained by setting the zirconia of the first layer to 30% or more.

  10 antifouling processed product, 20 antifouling coating film, 21 first layer, 22 second layer, 23 third layer

Claims (4)

A metal substrate and an antifouling coating film formed on the surface of the metal substrate,
The antifouling coating film is
A first layer formed on the metal substrate and including zirconium oxide;
A second layer formed on the first layer and comprising an alkali silicate;
A third layer formed on the second layer and including at least one selected from zirconium oxide, yttrium oxide, hafnium oxide, and rare earth oxide;
Antifouling processed product characterized by having.   2. The antifouling processed product according to claim 1, wherein the third layer contains 70% by mass or more of at least one selected from zirconium oxide, yttrium oxide, hafnium oxide, and rare earth oxide. .   The antifouling processed product according to claim 1 or 2, wherein the first layer contains 30 mass% or more of zirconium oxide. A coating solution containing a zirconium-containing component including at least one selected from zirconia sol, zirconium alkoxide, a partial hydrolysis product of the zirconium alkoxide, and a zirconium salt is applied on the surface of the metal substrate, and heat treatment is performed. Forming a first layer of the heat treatment product;
Applying a coating solution containing an alkali silicate on the first layer, performing a heat treatment, and forming a second layer made of the heat treatment product;
On the second layer, a coating solution containing at least one selected from sol, alkoxide and partially hydrolyzed product thereof, and salt of at least one component selected from zirconium, yttrium, hafnium and rare earth elements. Applying and heat treating to form a third layer of the heat treated product;
A method for producing an antifouling processed product, comprising:

Images