JP6134576B2 - Method for producing modified silica film, coating liquid, and modified silica film - Google Patents

Description

  The present invention relates to a method for producing a modified silica film, a coating liquid, and a modified silica film.

  Silica film produced by converting (or curing) polysilazane to silica has a strength close to that of glass, so it is used to improve the surface strength of various films. Often. In recent years, there is an increasing need to improve the surface strength of optical films (film) using such silica films. Here, the optical film is, for example, an antireflection film attached to the surface of the display.

  Such an optical film is required to have good scratch resistance and antifouling properties, but the silica film produced by converting polysilazane is not sufficiently scratch resistant and antifouling. Therefore, it is necessary to modify the silica film. Patent Document 1 proposes a method of converting polysilazane to silica after adding a water / oil repellency-imparting agent to polysilazane as a method of modifying the silica film. Here, the water / oil repellency imparting agent is a reactive fluoropolymer having a linking group capable of binding to polysilazane.

JP 2006-82341 A

  However, since polysilazane is very reactive, simply adding a reactive fluororesin to polysilazane causes the polysilazane to react with the reactive fluoropolymer before the polysilazane is converted to silica. And the reaction point which reacted with the reactive fluoropolymer among polysilazane does not bridge | crosslink with the surrounding silica frame | skeleton in the case of silica conversion. Therefore, the crosslink density of the modified silica film decreases, and as a result, the strength of the modified silica film decreases. Thus, the technique disclosed in Patent Document 1 has a problem that the strength of the modified silica film is reduced. The reaction between the reactive fluoropolymer and polysilazane is confirmed by a decrease in strength of the modified silica film. However, some reactive fluoropolymers cause the polysilazane solution to become clouded by reaction with polysilazane, and thus the reaction between the reactive fluoropolymer and polysilazane can be confirmed by such clouding.

  As a method for solving such a problem, a so-called two-layer coating method has been proposed. In the two-layer coating method, a polysilazane solution in which only polysilazane is dissolved is first coated on an optical film and dried to convert the polysilazane to silica. Thereby, a silica film, that is, a hard coat layer is formed on the optical film. And a protective layer is formed on a hard-coat layer by apply | coating and drying a reactive fluoropolymer solution on a hard-coat layer.

  However, in this two-layer coating method, the coating has to be performed twice, and each coating has to be performed with high accuracy (for example, so that the defect becomes zero). Therefore, there is another problem that it takes much time to produce the hard coat layer and the protective layer. Due to such problems, an optical film having a hard coat layer and a protective layer produced by a two-layer coating method is very expensive and has not become a general-purpose product.

  Therefore, the present invention has been made in view of the above problems, and an object of the present invention is to provide a modified silica film that can easily produce a modified silica film having a higher strength than conventional ones. It is in providing a manufacturing method, a coating liquid, and a modified silica film.

  In order to solve the above problems, according to an aspect of the present invention, a step of preparing a reactive fluoropolymer solution by dissolving a reactive fluoropolymer having a bonding group that binds to polysilazane in a fluorosolvent, A step of preparing a polysilazane solution by dissolving polysilazane in a solvent for polysilazane which is not miscible with the reactive fluoropolymer and has a higher surface tension than the reactive fluoropolymer and a fluorine solvent, and mixing the polysilazane solution and the reactive fluoropolymer solution Then, a step of producing a coating liquid, a step of producing a coating layer by coating the coating liquid on a substrate, a step of removing the polysilazane solvent and the fluorine solvent from the coating layer, Bonding a linking group to the polysilazane and converting the polysilazane to silica, comprising the steps of: The mass ratio of Razan to the reactive fluoropolymer is 99: 1 to 90:10, and the reactive fluoropolymer solution contains 1 to 30% by mass of the reactive fluoropolymer with respect to the total mass of the reactive fluoropolymer solution. The method for producing a modified silica film is characterized in that the fluorine solvent has a boiling point of 61 ° C. or higher.

  From this viewpoint, the reactive fluoropolymer solution in the coating layer naturally bleeds out on the surface of the coating layer. Therefore, according to this viewpoint, the modified silica film, that is, the hard coat layer and the protective layer can be formed only by coating one layer of the coating liquid on the substrate. Therefore, a modified silica film can be easily produced. Furthermore, since the reactive fluoropolymer solution bleeds out on the surface of the coating layer in the coating layer, the reaction between the reactive fluoropolymer and polysilazane is suppressed. Therefore, the strength of the modified silica film is improved as compared with the conventional modified silica film.

  Here, the value obtained by subtracting the larger value of the surface tensions of the reactive fluoropolymer and the fluorine solvent from the surface tension of the polysilazane solvent may be 5 or more.

  According to this viewpoint, the reactive fluoropolymer solution can bleed out to the surface of the coating layer more efficiently.

  The solvent for polysilazane may be a hydrophobic and nonpolar organic solvent.

  According to this aspect, the polysilazane solvent is a hydrophobic and nonpolar organic solvent and is not miscible with the fluorine solvent. Therefore, the reactive fluoropolymer solution can bleed out to the surface of the coating layer more efficiently.

  The solvent for polysilazane may be composed of any one or more selected from the group consisting of dibutyl ether, xylene, mineral terpenes, petroleum hydrocarbons, and high-boiling aromatic hydrocarbons.

  According to this aspect, the polysilazane solvent is composed of at least one selected from the group consisting of dibutyl ether, xylene, mineral terpenes, petroleum hydrocarbons, and high-boiling aromatic hydrocarbons. These solvents are not miscible with the fluorine solvent. Therefore, the reactive fluoropolymer solution can bleed out to the surface of the coating layer more efficiently.

  The fluorine solvent may be a hydrofluoroether.

  According to this viewpoint, the fluorine solvent is composed of hydrofluoroether. This solvent has a lower surface tension than the polysilazane solvent and is not miscible with the polysilazane solvent. Therefore, the reactive fluoropolymer solution can bleed out to the surface of the coating layer more efficiently.

  According to another aspect of the present invention, a reactive fluoropolymer solution prepared by dissolving a reactive fluoropolymer having a linking group that binds to polysilazane in a fluorosolvent, and is not miscible with the fluorosolvent and is reactive. And a polysilazane solution prepared by dissolving polysilazane in a solvent for polysilazane having a surface tension higher than that of the fluorine polymer and the fluorine solvent, and the mass ratio of the polysilazane to the reactive fluoropolymer is 99: 1 to 90:10 The reactive fluoropolymer solution contains 1 to 30% by mass of the reactive fluoropolymer based on the total mass of the reactive fluoropolymer solution, and the fluorine solvent has a boiling point of 61 ° C. or higher. A working fluid is provided.

  When the coating layer is formed by coating the coating liquid according to this viewpoint on the substrate, the reactive fluoropolymer solution naturally bleeds out on the surface of the coating layer. Therefore, a modified silica film, that is, a hard coat layer and a protective layer can be formed only by coating one layer of the coating liquid according to this viewpoint on the substrate. Therefore, a modified silica film can be easily produced. Furthermore, since the reactive fluoropolymer solution bleeds out on the surface of the coating layer in the coating layer, the reaction between the reactive fluoropolymer and polysilazane is suppressed. Therefore, the strength of the modified silica film is improved as compared with the conventional modified silica film.

  According to another aspect of the present invention, there is provided a modified silica film produced by the method for producing a modified silica film.

  The modified silica film according to this aspect is divided into a hard coat layer containing silica and a protective layer containing a reactive fluoropolymer. And the crosslinking density of the silica in a hard-coat layer is higher than the crosslinking density of the conventional modified silica film. This is because the reaction between the polysilazane and the reactive fluoropolymer is suppressed according to the method for producing the modified silica film. Therefore, the strength of the modified silica film is higher than before. Furthermore, in the method for producing the modified silica film described above, the modified silica film can be formed only by coating one layer of the coating liquid on the substrate. Therefore, the modified silica film is easily produced.

  According to another aspect of the present invention, a hard coat layer containing silica converted from polysilazane and a fluoropolymer bonded to the surface of the hard coat layer, the average surface roughness is 3.0 to 9.0 nm A modified silica membrane characterized in that it comprises a layer.

  In this respect, since the average surface roughness of the modified silica film is 3.0 to 9.0 nm, at least one of the scratch resistance and the oleic acid falling angle is improved.

  As described above, according to the present invention, the reactive fluoropolymer solution in the coating layer naturally bleeds out on the surface of the coating layer. Therefore, according to this viewpoint, the modified silica film, that is, the hard coat layer and the protective layer can be formed only by coating one layer of the coating liquid on the substrate. Therefore, a modified silica film can be easily produced. Furthermore, since the reactive fluoropolymer solution bleeds out on the surface of the coating layer in the coating layer, the reaction between the reactive fluoropolymer and polysilazane is suppressed. Therefore, the strength of the modified silica film is improved as compared with the conventional modified silica film.

It is a schematic diagram which shows the outline | summary of the manufacturing method of the modified silica film which concerns on embodiment of this invention, and a modified silica film. It is a schematic diagram of the coating liquid concerning the embodiment. It is a schematic diagram of the reactive fluoropolymer solution micelle (micell) disperse | distributed in the coating liquid. It is a schematic diagram which expands and shows the surface of the modified silica film which concerns on this embodiment. It is a schematic diagram which expands and shows the surface of the modified silica film produced by the conventional two-layer coating method. It is a schematic diagram which shows the structure of the test apparatus used for a pencil rubbing test.

  Exemplary embodiments of the present invention will be described below in detail with reference to the accompanying drawings. In addition, in this specification and drawing, about the component which has the substantially same function structure, duplication description is abbreviate | omitted by attaching | subjecting the same code | symbol. The surface tension is a value at 25 ° C., and the unit is (mN / m). The surface tension is measured by, for example, an automatic surface tension meter (specifically, Kyowa Interface Science DY-300). The surface tensions of examples and comparative examples described later are those measured by Kyowa Interface Science DY-300. Of course, the surface tension may be measured by other known methods.

<1. Method for producing modified silica film>
First, based on FIGS. 1-3, the manufacturing method of the modified silica film which concerns on this embodiment is demonstrated. The method for producing a modified silica film according to the present embodiment is divided into first to sixth steps.

  The first step is a step of preparing a polysilazane solution 11 shown in FIG. 2 by dissolving polysilazane in a polysilazane solvent. The second step is a step of preparing the reactive fluoropolymer solution 12 by dissolving the reactive fluoropolymer 13 shown in FIG. The order of the first step and the second step is not particularly limited.

  The third step is a step of preparing the coating liquid 10 shown in FIG. 2 by mixing the polysilazane solution 11 and the reactive fluoropolymer solution 12. A 4th step is a step which produces a coating layer by coating the coating liquid 10 on the base material 100, as shown in FIG. The fifth step is a step of removing the polysilazane solvent and the fluorine solvent 14 from the coating layer. The sixth step is to bind the reactive fluoropolymer to the polysilazane and convert the polysilazane to silica. Through these steps, the modified silica film 1 is formed on the substrate 100. The modified silica film 1 includes a hard coat layer 20 containing silica and a protective layer 30 containing a reactive fluoropolymer. That is, in the present embodiment, the hard coat layer 20 and the protective layer 30 containing a reactive fluoropolymer are produced by one-layer coating of the coating liquid 10. Hereinafter, each step will be described.

(First step)
The first step is a step of preparing a polysilazane solution 11 by dissolving polysilazane in a solvent for polysilazane.

  Polysilazane is an inorganic polymer that is also referred to as perhydropolysilazane, and has a structure represented by the following chemical formula (1). In chemical formula (1), n is a natural number.

  The weight average molecular weight of polysilazane is preferably as low as possible. This is because the higher the weight average molecular weight of polysilazane, the easier it is for polysilazane to precipitate as crystals in the polysilazane solution 11.

  The solvent for polysilazane is a solvent that satisfies the following requirements. That is, (1) Polysilazane is dissolved. (2) Not miscible with the fluorine solvent 14. (3) The surface tension is higher than that of the reactive fluoropolymer 13 and the fluorine solvent 14. When the solvent for polysilazane satisfies these requirements, the reactive fluoropolymer solution 12 in the coating layer can be bleed out to the surface of the coating layer. That is, the reactive fluoropolymer solution 12 is drawn to the atmosphere side.

  That is, when the polysilazane solvent is not miscible with the fluorine solvent 14, the reactive fluoropolymer solution 12 can exist as fine micelles in the coating solution 10 as shown in FIGS. 2 and 3. Further, the reaction between the reactive fluoropolymer 13 and polysilazane is also suppressed. The surface tension of the polysilazane solvent is higher than the surface tension of the reactive fluoropolymer 13 and the fluorine solvent 14. Further, repulsive force from the polysilazane solvent acts on the micelles of the reactive fluoropolymer solution 12. Therefore, the reactive fluoropolymer solution 12 can bleed out on the surface of the coating layer. The arrow A in FIG. 2 shows how the reactive fluoropolymer solution 12 bleeds out.

  From the above viewpoint, the difference between the surface tension of the polysilazane solvent and the surface tension of the reactive fluoropolymer 13 and the fluorine solvent 14 is preferably as large as possible. This is because the greater the difference, the easier the reactive fluoropolymer solution 12 will bleed out on the surface of the coating layer. More specifically, the value obtained by subtracting the larger value of the surface tensions of the reactive fluoropolymer 13 and the fluorine solvent 14 from the surface tension of the polysilazane solvent is preferably 5 or more.

  Examples of the solvent for polysilazane that satisfies the above requirements include hydrophobic and nonpolar organic solvents. Examples of the organic solvent include dibutyl ether, xylene, mineral turpentine, petroleum hydrocarbons, and high-boiling aromatic hydrocarbons. Therefore, the polysilazane solvent is preferably composed of at least one selected from the group consisting of dibutyl ether, xylene, mineral terpenes, petroleum hydrocarbons, and high-boiling aromatic hydrocarbons. The surface tension of dibutyl ether is 22.4, the surface tension of xylene is 30.0, and the surface tension of mineral terpenes is 25.0.

  In the polysilazane solution 11, an additive that does not deteriorate the polysilazane may be arbitrarily dissolved. For example, the polysilazane solution 11 may contain an amine-based catalyst. When the polysilazane solution 11 contains an amine-based catalyst, the silica conversion of the polysilazane can be performed at room temperature. Polysilazane is converted to silica even when heated to about 300 to 400 ° C., but in this treatment, the optical film serving as the substrate is subjected to thermal stress. Therefore, for example, when it is not desired to apply heat stress to the optical film, an amine-based catalyst may be included in the polysilazane solution 11.

  The water content of the polysilazane solvent is preferably as low as possible. For example, the water content of the polysilazane solvent is preferably less than 1% by mass (mass% of water relative to the total mass of the solvent for polysilazane). This is because water in the polysilazane solvent causes silica conversion of the polysilazane. Such silica conversion deteriorates the quality of the modified silica film 1.

(Second step)
The second step is a step of preparing the reactive fluoropolymer solution 12 by dissolving the reactive fluoropolymer 13 in the fluorine solvent 14.

  As shown in FIG. 3, the reactive fluoropolymer 13 includes a fluoropolymer main chain 13A and a bonding group 13B. The reactive fluoropolymer 13 is specifically represented by the following chemical formula (2).

  In chemical formula (2), Rf2 is a (per) fluoroalkyl group or (per) fluoropolyether group, W2 is a linking group, and X is a linking group 13B. Therefore, in the chemical formula (2), other than X is the fluoropolymer main chain 13A.

The structure of the (per) fluoroalkyl group is not particularly limited. That is, the (per) fluoroalkyl group is a straight chain (for example, —CF ₂ CF ₃ , —CH ₂ (CF ₂ ) ₄ H, —CH ₂ (CF ₂ ) ₈ CF ₃ , —CH ₂ CH ₂ (CF ₂ ). ₄ H, etc.) even in a branched structure (eg, CH (CF ₃ ) ₂ , CH ₂ CF (CF ₃ ) ₂ , CH (CH ₃ ) CF ₂ CF ₃ , CH (CH ₃ ) (CF ₂ ) ₅ CF ₂ H or the like, but an alicyclic structure (preferably a 5- or 6-membered ring such as a perfluorocyclohexyl group, a perfluorocyclopentyl group, or an alkyl group substituted with these. Etc.).

The (per) fluoropolyether group is a (per) fluoroalkyl group having an ether bond, and the structure thereof is not particularly limited. That is, as the (per) fluoropolyether group, for example, CH ₂ OCH ₂ CF ₂ CF ₃ , CH ₂ CH ₂ OCH ₂ C ₄ F ₈ H, CH ₂ CH ₂ OCH ₂ CH ₂ C ₈ F ₁₇ , CH ₂ CH ₂ OCF ₂ CF ₂ OCF ₂ CF ₂ H, a fluorocycloalkyl ether group having 4 to 20 carbon atoms having 5 or more fluorine atoms, and the like. Other examples include (CF ₂ ) _x O (CF ₂ CF ₂ O) _y , [CF (CF ₃ ) CF ₂ O] _x- [CF ₂ (CF ₃ )], (CF ₂ CF ₂ CF ₂ O) _x , (CF ₂ CF ₂ O) _{x and the} like. Here, x and y are arbitrary natural numbers.

  When Rf2 is a (per) fluoroalkyl group, the linking group is a divalent functional group having at least an ether bond. Examples of such a divalent functional group include those obtained by changing the methyl terminal of the examples listed as (per) fluoropolyether groups to methylene groups. On the other hand, the linking group is not particularly limited when Rf2 is a (per) fluoropolyether group. In this case, examples of the linking group include a methylene group, a phenylene group, an alkylene group, an arylene group, a heteroalkylene group, and a combination group of these. It is done. These linking groups may further have a carbonyl group, a carbonyloxy group, a carbonylimino group, a sulfonamide group, or a functional group that combines these groups. Can be mentioned. Examples of the photopolymerizable functional group include an acryloyl group and a methacryloyl group. Therefore, the fluoropolymer main chain 13A is a (per) fluoropolyether group as a whole.

  The bonding group 13B is a functional group that bonds to polysilazane, and is, for example, an alkoxy group having 1 to 4 carbon atoms, a silanol group (hydroxyl group), halogen, or hydrogen. n represents 1-3. The weight average molecular weight of the reactive fluoropolymer 13 is not particularly limited, but is, for example, 10,000 or more.

  The reactive fluoropolymer 13 has a very low surface tension, for example, 16.5 or less. Therefore, the difference from the surface tension of the polysilazane solvent is 5 or more.

  The fluorine solvent 14 is an organic solvent containing fluorine and having a boiling point of 61 ° C. or higher. Examples of the fluorine solvent 14 include hydrofluoroether. That is, the fluorine solvent 14 is composed of any one or more selected from these solvents. The surface tension of the fluorine solvent 14 is very low, for example, 15 or less. Therefore, the difference from the surface tension of the polysilazane solvent is 5 or more. In addition, as shown by the comparative example mentioned later, when the fluorine solvent 14 whose boiling point is less than 61 degreeC is used, the antifouling property of the modified silica film 1 falls.

  The concentration of the reactive fluoropolymer solution 12, that is, the mass% of the reactive fluoropolymer 13 with respect to the total mass of the reactive fluoropolymer solution 12 is 1 to 30 mass%. When the concentration of the reactive fluoropolymer solution 12 is less than 1% by mass, that is, when the fluorine solvent 14 is too much with respect to the reactive fluoropolymer 13, the reactive fluoropolymer solution 12 is stably present in the coating solution 10. Can not do it. Specifically, the polysilazane solution 11 and the reactive fluoropolymer solution 12 are completely separated in the coating solution 10. More specifically, the reactive fluoropolymer solution 12 is not dispersed in the polysilazane solution 11 as micelles but separated from the polysilazane solution 11 as a liquid layer. As a result, the coating liquid 10 may become cloudy. Further, the crosslink density of silica after silica conversion is lowered, and consequently the strength of the modified silica film is lowered.

  On the other hand, when the concentration of the reactive fluoropolymer solution 12 is larger than 30% by mass, that is, when the reactive fluoropolymer 13 is too much with respect to the fluorine solvent 14, the reactive fluoropolymer 13 reacts with polysilazane in the coating solution 10. There is a possibility that. That is, the crosslink density of silica after silica conversion is lowered, and consequently the strength of the modified silica film is lowered.

  According to Examples described later, the concentration of the reactive fluoropolymer solution 12 is preferably 3 to 20% by mass, and more preferably 5 to 10% by mass.

(Third step)
The third step is a step of preparing the coating liquid 10 by mixing the polysilazane solution 11 and the reactive fluoropolymer solution 12.

  When the reactive fluoropolymer 13 is simply included in the polysilazane solution 11, the bonding group 13B of the reactive fluoropolymer 13 reacts with the polysilazane. And the reaction point which reacted with the reactive fluoropolymer 13 among polysilazane does not bridge | crosslink with the surrounding silica frame | skeleton in the case of silica conversion. Therefore, the crosslink density of the modified silica film decreases, and as a result, the strength of the modified silica film decreases.

  Therefore, in this embodiment, the reactive fluoropolymer solution 12 is prepared by dissolving the reactive fluoropolymer 13 in the fluorine solvent 14. And the reactive fluoropolymer solution 12 and the polysilazane solution 11 are mixed, and the coating liquid 10 shown in FIG. 2 is produced. Since the solvent for polysilazane is not miscible with the fluorine solvent 14, the reactive fluoropolymer solution 12 exists as micelles in the coating solution 10. Moreover, since the reactive fluoropolymer 13 exists in the fluorine solvent 14, reaction with polysilazane is suppressed. Similarly, the fluorine solvent 14 does not react with polysilazane. Accordingly, the polysilazane is stably present in the coating solution 10. Thereby, the storage stability of the coating liquid 10 is ensured.

  The surface tension of the reactive fluoropolymer solution 12 (that is, the surface tension of the reactive fluoropolymer 13 and the surface tension of the fluorine solvent 14) is much lower than the surface tension of the polysilazane solvent. Furthermore, a repulsive force from the polysilazane solution 11 also acts on the reactive fluoropolymer solution 12. Therefore, the reactive fluoropolymer solution 12 bleeds out on the surface of the coating layer.

  Here, the mass ratio of the polysilazane and the reactive fluoropolymer 13 in the coating liquid 10 is 99: 1 to 90:10. When the mass ratio of the reactive fluoropolymer 13 exceeds 10, that is, when the reactive fluoropolymer 13 is too much relative to the polysilazane, the reactive fluoropolymer 13 may react with the polysilazane. That is, the crosslink density of silica after silica conversion may be reduced. On the other hand, when the mass ratio of the reactive fluoropolymer 13 is less than 1, that is, when the polysilazane is too much with respect to the reactive fluoropolymer 13, the protective layer 30 having a sufficient thickness is not formed. According to the Example mentioned later, 97: 3-93: 7 is preferable and, as for mass ratio of the polysilazane in the coating liquid 10, and the reactive fluoropolymer 13, 97: 3-95: 5 is more preferable.

(Fourth step)
The fourth step is a step of applying the coating liquid 10 onto the substrate 100 as shown in FIG. In addition, the coating method is not particularly limited, and a known method is arbitrarily applied. FIG. 1 shows a die coating method (a method of coating the coating liquid 10 on the substrate 100 through the die slit 450) as an example of coating. By the fourth step, a coating layer (a layer made of the coating solution 10) is formed on the substrate 100. The reactive fluoropolymer solution 12 in the coating layer bleeds out on the surface of the coating layer. Note that the base material 100 is a film to which the function of the modified silica film 1 is imparted. When the function by the modified silica film 1 is imparted to the optical film, the substrate 100 is an optical film.

(Fifth step)
The fifth step is a step of removing the polysilazane solvent and the fluorine solvent 14 from the coating liquid 10 on the substrate 100, that is, the coating layer. These solvents are removed, for example, by heating the coating layer at 100 ° C. for about 1 minute.

(Sixth step)
The sixth step is a step in which the reactive fluoropolymer 13 is bonded to polysilazane and the polysilazane is converted (cured) to silica. When the polysilazane solution contains an amine-based catalyst, these reactions proceed at room temperature. When the amine solvent is not contained in the polysilazane solution, these reactions proceed, for example, by heating the coating layer at 300 to 400 ° C. Of the coating layer, the portion where polysilazane is mainly distributed becomes the hard coat layer 20, and the portion where the reactive fluoropolymer 13 is mainly distributed becomes the protective layer 30. Through the above steps, the modified silica film 1 is formed on the substrate 100. In the silica conversion process, a reaction represented by the following chemical formula (3) occurs.

<2. Structure and Properties of Modified Silica Film>
Next, the structure and characteristics of the modified silica film 1 will be described with reference to FIGS. 1, 4, and 5.

  As shown in FIGS. 1 and 4, the modified silica film 1 has a hard coat layer 20 and a protective layer 30. The hard coat layer 20 includes silica formed by converting polysilazane into silica. The protective layer 30 includes the reactive fluoropolymer 13. The reactive fluoropolymer 13 is bonded to the silica of the hard coat layer 20 through the bonding group 13B.

  Here, the protective layer 30 is formed by bleeding out the reactive fluoropolymer 13 in the coating layer. That is, the method for producing a modified silica film according to the present embodiment does not artificially distribute the reactive fluoropolymer 13 on the surface of the hard coat layer 20 as in the conventional two-layer coating method. The reactive fluoropolymer 13 is naturally distributed on the surface of the layer 20.

  Therefore, the silica concentration distribution (silicon atom concentration distribution) and the reactive fluorine polymer 13 concentration distribution (fluorine atom concentration distribution) change gradually at the boundary between the hard coat layer 20 and the protective layer 30. That is, the silicon atom concentration in the vicinity of the surface of the substrate 100 is approximately 100 at%, but as the distance from the measurement point to the substrate 100 increases, the silicon atom concentration at the measurement point decreases and the fluorine atom concentration increases. At the point, the atomic concentration of both is the same value. In the present embodiment, a plane where the atomic concentrations of both are the same value is defined as a boundary surface 20A between the hard coat layer 20 and the protective layer 30. At the measurement point closer to the surface of the modified silica film 1 than the boundary surface 20A, the fluorine atom concentration is higher than the silicon atom concentration, and the fluorine atom concentration is approximately 100 at% on the surface of the modified silica film 1.

  Furthermore, as shown in FIG. 4, irregularities are formed on the surface of the protective layer 30. That is, the surface of the modified silica film 1 is rough (uneven). The following can be considered as this reason. That is, in the present embodiment, the boundary surface 20A between the hard coat layer 20 and the protective layer 30 is formed by bleed-out (natural movement) of the reactive fluoropolymer 13, so that the hard coat layer 20 and the protective layer 30 are The boundary surface 20A becomes rough (unevenness is formed). Therefore, the surface of the protective layer 30 formed on the surface becomes rough. The surface shape of the protective layer 30 can be confirmed, for example, by observation with a scanning electron microscope (SEM) or a shape measuring laser microscope. Here, the shape measurement laser microscope obtains three-dimensional data of the entire observation visual field by performing non-contact three-dimensional measurement of an object using a laser. Examples of the shape measuring laser microscope include VK-9500 manufactured by KEYENCE JAPAN. Of course, the shape measuring laser microscope is not limited to this example.

  On the other hand, as shown in FIG. 5, in the modified silica film produced by the conventional two-layer coating method, first, the hard coat layer 200 containing silica is produced, and then the protective layer 300 containing the reactive fluoropolymer 13 is formed. It is formed on the hard coat layer 200. Therefore, the boundary surface 200A between the hard coat layer 200 and the protective layer 300 is very flat.

  When the modified silica film 1 according to the present embodiment is compared with the conventional modified silica film, in the present embodiment, since the unevenness is formed on the boundary surface 20A, the area of the boundary surface 20A is larger than the conventional area. As a result, more reactive fluoropolymer 13 is distributed on the surface of the boundary surface 20A than before. Therefore, more reactive fluoropolymers 13 are in contact with the soil component 400 than in the past. Furthermore, in this embodiment, since the irregularities are formed on the surface of the protective layer 30, air enters between the dirt component 400 and the protective layer 30. Therefore, when the dirt component 400 is a liquid (for example, a liquid component in a fingerprint), the contact angle of the dirt component 400 is larger than the conventional one as shown in FIGS. Therefore, the surface of the modified silica film 1 is reduced.

  Further, the unevenness on the surface of the modified silica film 1 is gentle because it is formed by natural movement (bleed out) of the reactive fluoropolymer 13. Therefore, when the dirt component 400 is solid (for example, a wax component in a fingerprint), it is possible to prevent the dirt component 400 that has entered the recess from being removed (that is, sticking to the surface of the modified silica film 1).

  Moreover, as shown in the Examples described later, the average surface roughness Ra (nm) of the modified silica film 1 is preferably 3.0 or more and 9.0 or less. When the average surface roughness Ra (nm) is 3.0 or more and 9.0 or less, at least one of the scratch resistance and the oleic acid sliding angle is improved. Here, the average surface roughness Ra is an arithmetic average value of the heights of the convex portions of the protective layer 30, and the height of the convex portions is the lower end point of the concave portion adjacent to the convex portion from the apex of the convex portion (most hardest It is a distance to a point close to the coat layer 20. These values are measured by a shape measuring laser microscope. In the following examples and comparative examples, the average surface roughness was measured with VK-9500 manufactured by KEYENCE JAPAN.

Example 1
Next, examples of the present embodiment will be described. In Example 1, a modified silica film was produced by the following production method.

  AZ Electromaterials NAX120-20 was prepared as a stock solution of the polysilazane solution. Hereinafter, this stock solution is also referred to as “polysilazane stock solution”. The polysilazane stock solution contains 20% by mass of polysilazane with respect to the total mass of the polysilazane stock solution. The solvent of the polysilazane stock solution is dibutyl ether and contains an amine-based catalyst.

  Next, a predetermined amount of dibutyl ether was added to 9.9 parts by mass of the polysilazane stock solution and gently stirred for 10 minutes. This produced the polysilazane solution. Here, the amount of dibutyl ether added to the polysilazane stock solution was determined so that the mass part of the solid content (polysilazane + reactive fluoropolymer) in the coating solution described later was 2.

  On the other hand, KY-164 (surface tension 16.1) manufactured by Shin-Etsu Chemical Co., Ltd. was prepared as a reactive fluoropolymer, and Novec 7200 (surface tension 13.6, boiling point 76 ° C.) manufactured by Sumitomo 3M Co. was prepared as a fluorine solvent. . Novec 7200 and Novec 7000, Novec 7100, and Novec 7300 described later are all hydrofluoroethers.

  Next, a reactive fluoropolymer solution containing 20% by mass of the reactive fluoropolymer (% by mass with respect to the total mass of the reactive fluoropolymer solution) was prepared by dissolving the reactive fluoropolymer in a fluorine solvent.

  Next, 0.1 part by mass of a reactive fluoropolymer solution was added to the polysilazane solution and stirred for 10 minutes. This produced the coating liquid. The coating liquid contains 2 parts by mass of solid content (polysilazane + reactive fluoropolymer) and 98 parts by mass of solvent. A part of the coating solution was stored for evaluation described later.

  Then, a coating solution was applied on a PMMA (Poly (methyl methacrylate)) substrate so that the layer thickness of the modified silica film was about 200 nm. The coating was performed using a wire bar. This produced the coating layer. As described above, the reactive fluoropolymer solution in the coating layer bleeds out on the surface of the coating layer. Subsequently, the solvent was removed from the coating layer by heating the coating layer at 100 ° C. for 1 minute. All the above treatments were performed in a nitrogen atmosphere.

  Thereafter, the coating layer was allowed to stand at room temperature (23 ° C., relative humidity 54%) for 1 week. Thereby, the silica conversion of polysilazane and the bonding reaction between the reactive fluoropolymer and polysilazane proceeded. That is, a modified silica film was produced.

(Examples 2-14, Comparative Examples 1-10)
The same treatment as in Example 1 was performed except that the mass ratio of polysilazane and reactive fluoropolymer, the type of reactive fluoropolymer, the type of fluorosolvent, the presence or absence of the fluorosolvent, and the concentration of the reactive fluoropolymer solution were changed. It was. Table 1 summarizes the mass parts of the solid content in Examples 1 to 14 and Comparative Examples 1 to 10, the mass ratio of polysilazane and reactive fluoropolymer, the presence or absence of a fluorine solvent, and the concentration of the reactive fluoropolymer solution.

In the column of reactive fluoropolymers (fluoropolymer), * 1 indicates KY-108 (surface tension 16.5) manufactured by Shin-Etsu Chemical Co., Ltd. * 2 indicates OPTOOL DSX (surface tension 15.5) manufactured by Daikin Industries, Ltd. 9) and * 3 indicates TSL-8257 (surface tension 16.8) manufactured by GE Toshiba Silicone. Here, the molecular formula of TSL-8257 is CF ₃ (CF ₂ ) ₅ CH ₂ CH ₂ Si (OMe) ₃ . Therefore, TSL-8257 is a perfluoroalkyl containing no perfluoropolyether, which is different from the reactive fluoropolymer of the present invention. No symbol indicates KY-164 manufactured by Shin-Etsu Chemical Co., Ltd.

  In the column of reactive fluoropolymer solution concentration (fluorine solution concentration), * 4 indicates Novec 7000 (surface tension 12.4, boiling point 34 ° C.) manufactured by Sumitomo 3M, and * 5 indicates Novec 7100 (surface) manufactured by Sumitomo 3M. * 6 indicates Novec 7300 (surface tension 15.0, boiling point 98 ° C.) manufactured by Sumitomo 3M. No mark indicates Novec7200 manufactured by Sumitomo 3M.

  As shown in Table 1, in Examples 1 to 14, the value obtained by subtracting the larger value of the surface tensions of the reactive fluoropolymer and the fluorine solvent from the surface tension of the polysilazane solvent is 5 or more. Further, the mass ratio between the polysilazane and the reactive fluoropolymer, and the concentration of the reactive fluoropolymer solution are values within the range shown in the present embodiment.

  In Comparative Example 1, only a single layer of silica film is formed (a protective layer is not formed). Comparative Examples 3, 6, and 7 correspond to the method disclosed in Patent Document 1 because the reactive fluoropolymer is simply added to the polysilazane solution.

(test)
Next, the following wipe rubbing test was performed on the modified silica films according to the respective examples and comparative examples.

The surface of the modified silica film was subjected to 10 reciprocating wears with a wipe while applying a load of 500 g / cm ^{2 in} the vertical direction (vertical direction). The wipe used was a Kim wipe wiper S-200 manufactured by Nippon Paper Crecia.

(Evaluation of coating solution)
The coating liquid prepared in each Example and Comparative Example was visually observed immediately after preparation (initial) and after storage for 12 hours. This confirmed the presence or absence of the cloudiness of the coating liquid.

(Contact angle (CA) evaluation)
Using a fully automatic contact angle meter DM700 (manufactured by Kyowa Interface Science Co., Ltd.), 2 μl of pure water was dropped on the modified silica film, and the contact angle was measured. The contact angle of the modified silica film before the wipe rub test (initial stage) and the contact angle of the modified silica film after the wipe rub test were measured, and the difference (ΔCA) between them was calculated. It can be said that as ΔCA is smaller, the performance deterioration due to wipe rubbing is smaller, that is, the scratch resistance is higher.

(Oleic acid falling angle evaluation)
The oleic acid falling angle was measured using a fully automatic contact angle meter DM700 (manufactured by Kyowa Interface Science Co., Ltd.). Specifically, 5 μl of oleic acid was dropped on the modified silica film before the wipe rubbing test to incline the modified silica film. The angle when the oleic acid started to move was defined as the oleic acid falling angle.

(Average surface roughness evaluation)
The average surface roughness (Ra) of the modified silica film before the wipe rubbing test was measured by VK-9500 manufactured by KEYENCE JAPAN.

(Pencil scrub test)
In order to evaluate the strength of the modified silica film, a pencil rubbing test based on JIS-K-5600 was performed. Here, based on FIG. 6, the test apparatus 500 used for the pencil rubbing test will be described. FIG. 6 shows a state in which a pencil rubbing test is performed on the modified silica film 1 according to this embodiment using the test apparatus 500.

  The test apparatus 500 includes an apparatus main body 500A, a level 502, a small moving weight 503, a fastener 504, and an O-shaped ring 505. A through-hole into which the pencil 501 is inserted is formed in the apparatus main body 500A. An angle θ between the length direction of the pencil 501 inserted into the through hole and the bottom surface of the apparatus main body 500A (that is, the surface of the modified silica film 1) is 45 degrees. The level 502 is a component for confirming that the apparatus main body 500A is horizontal. The small moving weight 503 is a component for adjusting the load applied to the core 501A of the pencil 501. The small moving weight 503 is movable in the direction of the arrow 503A. The fastener 504 fixes the pencil 501 in the apparatus main body 500A. The O-ring 505 is rotatably attached to the apparatus main body 500A. The O-shaped ring 505 moves the test apparatus 500 in the test direction by rolling on the modified silica film 1.

  Next, the method of the pencil rubbing test will be described. Here, a method of the pencil rubbing test will be described taking the pencil rubbing test of the modified silica film 1 (formed on the base material 100) according to the present embodiment as an example.

  First, the pencil 501 is inserted and fixed in the test apparatus 500. Next, the core of the pencil 500 is pressed against the modified silica film 1. Next, the level 502 confirms that the test apparatus 500 is level. Next, a load of 500 g is applied to the core 501A of the pencil 501 by adjusting the position of the small weight 503. Next, the test apparatus 500 is moved at a speed of 0.8 mm / second in the test direction shown in FIG. Thereby, the core 501 </ b> A of the pencil 501 rubs the surface of the modified silica film 1. The above process becomes a pencil rubbing test. Thereafter, the presence or absence of scratches is confirmed visually. When scratches are confirmed, the above-mentioned pencil rubbing test is performed with the hardness of the core 501A of the pencil 501 lowered. If no scratch is confirmed, the hardness of the core 501A of the pencil 501 is increased and the pencil rubbing test is performed. Then, the maximum hardness (pencil hardness) at which no scratch is confirmed is measured. This hardness is a parameter indicating the strength (scratch resistance) of the modified silica film 1. The pencil hardness increases in the order of 2H> H> F> HB> B.

(Contrast between Example and Comparative Example)
The test and evaluation results are summarized in Table 2.

(Presence or absence of cloudiness)
When Examples and Comparative Examples were compared, the coating liquids of Examples were not cloudy, but the coating liquids of Comparative Examples 2 to 7 were cloudy from the beginning. The coating liquid of Comparative Example 1 did not become cloudy because the reactive fluoropolymer was not contained in the coating liquid. Furthermore, the intensity | strength (pencil hardness) of Examples 1-14 became larger than the intensity | strength of Comparative Examples 1-10. In Comparative Examples 2 to 10, it is surmised that the reactive fluoropolymer and polysilazane reacted in the coating solution, and as a result, the crosslink density of the modified silica film decreased. The white turbidity in Comparative Examples 2 to 7 is presumed to be caused by the reaction between polysilazane and a reactive fluoropolymer. Since the silica film of Comparative Example 1 does not have a protective layer, the strength is low. On the other hand, in Examples 1-14, since a reactive fluoropolymer bleeds out to the surface of a coating liquid in a coating liquid, reaction with a reactive fluoropolymer and polysilazane is suppressed. Therefore, it is speculated that the crosslink density of the modified silica film is higher than those of Comparative Examples 2 to 10, and as a result, the strength is increased.

(Contact angle and sliding angle)
In Examples 1 to 14, in addition to the above, at least one of scratch resistance (ΔCA) and oleic acid sliding angle is superior to most comparative examples. As this reason, it is possible that the average surface roughness Ra of an Example is a value within the range of 3.0-9.0 nm. In addition, although the (DELTA) CA oleic acid falling angle of the comparative example 4 is a value about a part of Examples, the intensity | strength of the comparative example 4 is still lower than Examples 1-14. Further, when a protective layer was formed on the surface of the silica film of Comparative Example 1 by the conventional two-layer coating method, the average surface roughness of the protective layer was 2.1 nm. Therefore, the average surface roughness of this embodiment cannot be realized by the conventional two-layer coating method. At this time, initial CA was 108.5 °, ΔCA was 7.5 °, and oleic acid sliding angle was 9 °. At least one of the initial CA, ΔCA, and oleic acid sliding angle of each example is superior to the value of Comparative Example 1.

  From the above examples and comparative examples, it was proved that the modified silica film according to the present embodiment has higher strength than the conventional modified silica film.

  As described above, in the present embodiment, the coating liquid 10 is prepared by mixing the polysilazane solution 11 and the reactive fluoropolymer solution 12. And a coating layer is produced by coating the coating liquid 10 on the base material 100. FIG. The reactive fluoropolymer solution 12 in the coating layer naturally bleeds out on the surface of the coating layer. Therefore, in this embodiment, the modified silica film 1, that is, the hard coat layer 20 and the protective layer 30 can be formed only by coating one layer of the coating liquid 10 on the substrate 100. Therefore, the modified silica film 1 can be easily produced. Furthermore, since the reactive fluoropolymer solution 12 bleeds out to the surface of the coating layer in the coating layer, the reaction between the reactive fluoropolymer 13 and polysilazane is suppressed. Therefore, the strength of the modified silica film 1 is improved as compared with the conventional modified silica film.

  Furthermore, since the value obtained by subtracting the larger value of the surface tensions of the reactive fluoropolymer 13 and the fluorine solvent 14 from the surface tension of the polysilazane solvent is 5 or more, the reactive fluoropolymer solution 12 is applied more efficiently. Bleed out on the surface of the construction layer.

  Furthermore, since the solvent for polysilazane is a hydrophobic and nonpolar organic solvent, it is not miscible with the fluorine solvent 14. Therefore, the reactive fluoropolymer solution 12 can bleed out to the surface of the coating layer more efficiently.

  Furthermore, the polysilazane solvent is composed of at least one selected from the group consisting of dibutyl ether, xylene, mineral terpenes, petroleum hydrocarbons, and high-boiling aromatic hydrocarbons. These solvents are not miscible with the fluorine solvent 14. Therefore, the reactive fluoropolymer solution 12 can bleed out to the surface of the coating layer more efficiently.

  Furthermore, the fluorine solvent is composed of hydrofluoroether. These solvents have a lower surface tension than the polysilazane solvent and are not miscible with the polysilazane solvent. Therefore, the reactive fluoropolymer solution 12 can bleed out to the surface of the coating layer more efficiently.

  Furthermore, since the average surface roughness of the modified silica film 1 is 3.0 to 9.0 nm, at least one of the scratch resistance and the oleic acid falling angle is improved.

  The preferred embodiments of the present invention have been described in detail above with reference to the accompanying drawings, but the present invention is not limited to such examples. It is obvious that a person having ordinary knowledge in the technical field to which the present invention pertains can come up with various changes or modifications within the scope of the technical idea described in the claims. Of course, it is understood that these also belong to the technical scope of the present invention.

1 Modified Silica Film 10 Coating Solution 11 Polysilazane Solution 12 Reactive Fluoropolymer Solution 13 Reactive Fluoropolymer 14 Fluorine Solvent 20 Hard Coat Layer 30 Protective Layer

Claims (7)

Creating a reactive fluoropolymer solution by dissolving a reactive fluoropolymer having a linking group that binds to polysilazane in a fluorosolvent;
Creating a polysilazane solution by dissolving polysilazane in a solvent for polysilazane that is immiscible with the fluorine solvent and has a higher surface tension than the reactive fluoropolymer and the fluorine solvent;
Mixing the polysilazane solution and the reactive fluoropolymer solution to prepare a coating solution;
Coating the coating liquid on a substrate to produce a coating layer;
Removing the polysilazane solvent and the fluorine solvent from the coating layer;
Binding the linking group to the polysilazane, and converting the polysilazane to silica,
The mass ratio of the polysilazane and the reactive fluoropolymer in the coating solution is 99: 1 to 90:10,
The reactive fluoropolymer solution contains 1 to 30% by mass of the reactive fluoropolymer with respect to the total mass of the reactive fluoropolymer solution,
The method for producing a modified silica film, wherein the fluorine solvent has a boiling point of 61 ° C. or higher.   The modified silica film according to claim 1, wherein a value obtained by subtracting a larger value of the surface tensions of the reactive fluoropolymer and the fluorine solvent from the surface tension of the polysilazane solvent is 5 or more. Manufacturing method.   The method for producing a modified silica film according to claim 1 or 2, wherein the polysilazane solvent is a hydrophobic and nonpolar organic solvent.   The polysilazane solvent is composed of at least one selected from the group consisting of dibutyl ether, xylene, mineral terpenes, petroleum hydrocarbons, and high-boiling aromatic hydrocarbons. Item 4. A method for producing a modified silica film according to Item 3.   The method for producing a modified silica film according to claim 1, wherein the fluorine solvent is composed of hydrofluoroether. A reactive fluoropolymer solution prepared by dissolving a reactive fluoropolymer having a bonding group that binds to polysilazane in a fluorine solvent;
A polysilazane solution that is immiscible with the fluorine solvent and is prepared by dissolving polysilazane in a solvent for polysilazane having a surface tension higher than that of the reactive fluoropolymer and the fluorine solvent,
The mass ratio of the polysilazane and the reactive fluoropolymer is 99: 1 to 90:10,
The reactive fluoropolymer solution contains 1 to 30% by mass of the reactive fluoropolymer with respect to the total mass of the reactive fluoropolymer solution,
The coating liquid, wherein the fluorine solvent has a boiling point of 61 ° C. or higher.   A modified silica film produced by the method for producing a modified silica film according to claim 1.

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