TW201348356A - Anti-reflection composition and its manufacturing process and uses - Google Patents

Abstract

An anti-reflection composition and its manufacturing process are provided. The anti-reflection composition comprises a hollow particle with a hydroxyl group on its surface, having an average particle size of about 10 nm to about 200 nm and a porosity of a hollow portion of about 10% to about 90%, wherein the density of the hydroxyl group is above about 2%; and a binder, having groups which can form a chemical bond with the hydroxyl group. The anti-reflection composition can be used in an anti-reflection film, having improved wear resistance and scratch resistance and showing satisfied anti-reflection effect.

Description

Antireflection composition, its manufacturing method and use

The present invention relates to a composition comprising hollow particles; in particular, the present invention relates to an antireflective composition comprising hollow particles.

The reflected light is present at the interface of two media having different refractive indices. For example, the refractive index of air is 1, and the refractive index of the glass substrate and the plastic substrate is between 1.45 and 1.7. Generally, the reflected light of these substrates and the air interface accounts for about 4% to 6.5%. In optical components, such as camera lenses, monitors and other imaging systems, the reflection of light not only reduces the imaging intensity, but also causes stray light in the image plane, which reduces the contrast of the image and reduces the resolution. In solar cell systems, the reflection of light reduces the utilization of solar energy.

In the early stage, most of the industry will apply a single-layer film as an anti-reflective film on the surface of the substrate to eliminate reflected light, and control the refractive index and film thickness of the film material to a certain value, so that incident light is on the upper and lower surfaces of the film (two The reflected light from the side produces destructive interference to achieve an anti-reflective effect. Specifically, to produce destructive interference, the following two conditions must be met: Condition 1, the amplitude of the reflected light on both sides of the film needs to be the same, that is, n ₀ /n _f =n _f /n _s or n _f =(n ₀ . n _s ) ^0.5 (where n ₀ , n _f , and n _s are the refractive indices of air, film, and substrate, respectively); Condition 2, the optical path satisfies the interference of the reflected light phase, that is, the minimum thickness of the film satisfies Light is 1/4 of the optical path in the medium. Wherein, to satisfy the condition 1, the refractive index of the film material should be as low as a certain value. For example, the most common glass substrate or polymer substrate used in the visible light region has a refractive index of about 1.5, and when the incident medium is air, the film The refractive index of the layer should be as low as about 1.23. However, the lowest-index homogeneous solid material existing in nature is ice, and its refractive index is still as high as 1.35. Therefore, the conventional use of a single-layer film structure often fails to obtain an ideal effect of reducing reflected light.

In order to solve the above problems, there are many other studies on anti-reflection structures, including the preparation of gradient-graded anti-reflective structures using plasma etching techniques (see US 7,858,293), and anti-reflective structures of multilayer films (see CN 101431110 A and CN). 101793981 A) etc. Although these techniques can obtain good anti-reflection effects, they are limited in practical applications due to their complicated structure and high production cost. Furthermore, anti-reflection is usually applied to structures requiring a large area. These methods of manufacturing anti-reflective structures are difficult to meet practical needs. Other previous studies have used nanoparticle to provide a thin film with a porous structure (see CN 101638297 A and CN 101280155), which uses the pores between the particles to obtain a lower refractive index and better anti-reflection effect, but Since the contact between the particles and the substrate is a "point" and a "face", the abrasion resistance and scratch resistance of the formed film are poor, which affects the application of the film.

In view of this, the present invention provides an improved anti-reflective composition which is low in production cost and which can form a coating having excellent abrasion resistance and scratch resistance and a low refractive index through a simple application step, and is advantageously used as a coating. Anti-reflective film.

It is an object of the present invention to provide an antireflective composition comprising hollow particles having a hydroxyl group on the surface, having an average particle diameter of from about 10 nm to about 200 nm and a hollow portion of from about 10% to about 90%. Porosity, and the density of the hydroxyl group is greater than about 2%; and a binder having a group that can form a chemical bond with the hydroxyl group.

Another object of the present invention is to provide a method for preparing an antireflection composition, which comprises Included: (a) providing a hollow particle having a hydroxyl group on the surface; (b) providing a binder having a group capable of forming a chemical bond with the hydroxyl group; (c) mixing the hollow particle with the binder Providing a mixture; and (d) optionally maintaining the temperature of the mixture at a temperature of from about 0 ° C to about 100 ° C in the presence of a desired catalyst and/or water such that the hydroxyl group on the surface of the hollow particle The group of the binder reacts to form a chemical bond.

It is still another object of the present invention to provide an antireflection sheet comprising a film and a substrate, wherein the film is on at least one surface of the substrate and is formed of an antireflective composition as described above.

The detailed description of the present invention and the preferred embodiments thereof will be described in the following description.

The present invention may be embodied in a variety of different forms without departing from the spirit and scope of the invention. In addition, the terms "a", "an" and "the" Further, as used herein, "chemical bonding" refers to interatomic interactions that cause them to be stably brought together, particularly in the form of covalent bonding.

The antireflective composition of the present invention comprises a hollow particle having a hydroxyl group on its surface, and a binder having a group capable of forming a chemical bond with the hydroxyl group. When the antireflective composition of the present invention is applied to a surface of a substrate to form a film, the hollow structure of the hollow particles enables the film to have a lower refractive index and a higher light transmittance; A chemical bond may be formed between the hollow particles and the binder to enhance the bonding force between the hollow particles and the hollow particles and the substrate, so that the formed film has an appropriate strength.

As described above, the antireflection composition of the present invention is particularly useful for forming an antireflection film, so that its composition and amount are highly correlated with the desired properties of the formed film (e.g., refractive index, abrasion resistance, etc.). , the details will be explained below.

According to the antireflective composition of the present invention, the hollow particles generally have an average particle diameter of from about 10 nm to about 200 nm, preferably from about 20 nm to about 100 nm. It is known that the particle size of the hollow particles affects the thickness of the formed film; as mentioned above, one of the conditions for forming a film having a desired antireflection effect on the surface of the substrate is that the minimum thickness of the film satisfies the light in the medium. 1/4 of the optical path. Taking the longest wavelength of red light (wavelength of about 800 nm) as an example, the thickness of the formed film should not exceed about 200 nm, so it is not suitable to use hollow particles having an average particle diameter of more than about 200 nm. On the other hand, when the average particle diameter of the hollow particles is less than about 10 nm, the hollow particles are easily aggregated to make the thickness of the formed film uneven, resulting in poor antireflection effect.

The refractive index of the formed film can be expressed by the following formula (1): n _f = n _p . V _p +n _b . V _b +n ₀ . ε (1) wherein n _f , n _p , n _b , and n ₀ are the refractive index of the film, the material constituting the hollow particles, the binder, and air, respectively; V _p is the volume content of the particles (excluding the hollow portion) V _b is the volume content of the binder; ε is the porosity of the film. It can be seen from the formula (1) that the refractive index of the formed film is related to the refractive index and the amount of the constituent hollow particle material, the refractive index and the amount of the binder, and the porosity of the film, which can be provided by adjusting these parameters. A film having a desired refractive index.

In summary, when the composition and volume content of the hollow particles and the binder are fixed, the porosity of the hollow portion of the hollow particles (referring to the ratio of the volume of the hollow portion of the hollow particles to the total volume of the hollow particles) is larger. The lower the refractive index of the formed film. According to an embodiment of the present invention, the hollow portion of the hollow particle has a porosity of from about 10% to about 90%, preferably from about 20% to about 80%; and on the other hand, the hollow particle The hollow portion can have an average pore size of from about 20 nanometers to about 60 nanometers.

According to the foregoing condition for obtaining an ideal anti-reflection effect n _f = (n _s .n ₀ ) ^0.5 , the refractive index of the formed film is also related to the refractive index of the substrate material used, that is, the selection of the hollow particle material can be regarded as the substrate material. Depending on the refractive index (according to the above formula (1)). Specifically, in the related art, a glass substrate, a polymethyl methacrylate substrate, a polycarbonate substrate, or a polyethylene terephthalate substrate or the like is generally used as a substrate of an antireflection film. The refractive index of such substrates is between about 1.4 and about 1.6. In the case of a single layer coating, the refractive index of the formed film needs to be between about 1.2 and about 1.3 (n _f = (n _{s )} .n ₀ ) ^0.5 ); according to the above formula (1), when the composition and volume of the binder and the porosity of the film are fixed, to obtain a lower refractive index of the film, a material with a lower refractive index should be selected to prepare a hollow. Particles. Therefore, in one embodiment of the composition of the present invention, the material of the hollow particles is selected from the group consisting of cerium oxide, organic decane, and combinations thereof, having a refractive index lower than 1.4. And it is easy to produce hollow particles of nanometer size.

Further, the particle size uniformity of the hollow particles is also related to the properties of the formed antireflection film. Using an antireflective composition comprising hollow particles having a relatively uniform particle size, the thickness and refractive index of the film formed after application are relatively uniform, and thus the antireflection of the film Sex is also relatively stable. In one embodiment of the present invention, the polydispersity coefficient (Dv/Dn, Dv is a volume average particle diameter, and Dn is an average particle diameter) of the particle diameter of the hollow particles used is less than about 1.05.

The shape of the hollow particles which can be used in the antireflection composition of the present invention may include, but is not limited to, spherical, ellipsoidal, or peanut-shaped, etc., wherein the shape of the hollow particles can be controlled by a preparation process.

In the prior art, the surface of the hollow particles is usually chemically modified, for example, a decane coupling agent having a saturated or unsaturated hydrocarbon group, a mercapto group, an amine group, an epoxy group or the like, and a specific example is methyl trimethyl. Oxy decane, vinyl triethoxy decane, 3-mercaptopropyltrimethoxy decane, amine propyl triethoxy decane, 3-(methacryl oxirane) propyl trimethoxy decane, 2, 3 - glycidoxypropyltrimethoxydecane, and the like. However, modification of the surface of hollow particles such as cerium oxide reduces the hydroxyl content on the surface of the particles, which in turn affects the interaction between the hollow particles and the binder. This effect will be explained in the next paragraph.

The surface of the hollow particles used in the antireflective composition of the present invention contains a specific amount of hydroxyl groups which are not chemically modified by the above surface. Meanwhile, the anti-reflective composition of the present invention comprises, in addition to the hollow particles, a binder which forms a chemical bond with a hydroxyl group on the surface of the hollow particle, in particular, forms a covalent bond, such as -O- , -COO-, etc. Without being bound by theory, Xianxin can form a chemical bond between the hollow particles and the binder to avoid agglomeration (aggregation) of the hollow particles, so that the hollow particles are uniformly dispersed in the binder to avoid the subsequent formation of the film. The whitening phenomenon can simultaneously improve the interaction between the hollow particles and the formed film and the substrate, and enhance the abrasion resistance, scratch resistance and the like of the formed film.

Thus, in accordance with the antireflective compositions of the present invention, the density of the hydroxyl groups on the surface of the hollow particles is typically greater than about 2%, preferably greater than about 2.2%. As described above, if the density of the hydroxyl group is too low, it is disadvantageous for the action between the hollow particles and the binder, which lowers the properties of the formed film.

The binder useful in the present invention has a group capable of forming a chemical bond with a hydroxyl group, and the aforementioned group may be selected from the group consisting of -OH, -COOH, -CNH, -CONH-, -NCO, and the foregoing In combination, a chemical bond can be formed with the hydroxyl group. The binder suitable for use in the present invention may include, but is not limited to, an organic oxime resin, a modified organic oxime resin, an inorganic cerium sol, or a combination thereof, and the above organic oxime resin, for example, from chlorodecane, alkoxy decane or a polyorganosiloxane having a network structure formed by hydrolyzing polycondensation of the mixture (such as methyl hydrazine resin, phenyl hydrazine resin, methyl phenyl hydrazine resin), or a monofunctional chain segment (R ₃ SiO _0.5 ) and four An MQ resin composed of a functional chain (SiO ₂ ); a modified organic oxime resin as described above, such as an epoxy, polyester, polyurethane, phenolic or the like; and the above-mentioned inorganic cerium sol, such as an acid catalyzed Oxide sol.

According to the antireflection composition of the present invention, the hollow particles may be included in an amount of from about 1 part by weight to about 20 parts by weight, based on 100 parts by weight of the binder, preferably from 4 parts by weight to about 15 parts by weight. If the proportion of the hollow particles is too low, the refractive index of the formed film cannot be effectively lowered; if it is too high, the formed film is easily damaged due to insufficient adhesion.

According to an embodiment of the present invention, in the antireflective composition, at least a portion of the hydroxyl group on the surface of the hollow particle forms a chemical bond with at least a portion of the group of the binder, particularly Covalent bond.

The antireflective composition of the present invention includes any conventional knowledge in the art, as needed The additive known in the art, according to the antireflective composition of the present invention, may be included in an amount of from about 0 part by weight to about 20 parts by weight based on 100 parts by weight of the above-mentioned binder. The above additives may include, depending on their use requirements and uses, thickeners that maintain a certain viscosity of the composition during the application process (eg, coating) (eg, including but not limited to: ethylene glycol, glycerol, xanthan gum, Polyvinyl alcohol, polyethylene glycol); a dispersant that can help the hollow particles to be uniformly dispersed in the binder (for example, including but not limited to: polyacrylic acid, polyvinyl alcohol, polyethylene glycol); a dispersing agent (for example, including but not Limited to: polyacrylic acid, polyvinyl alcohol, polyethylene glycol, sodium benzoate); bridging agents (such as, but not limited to, polyisocyanates); solvents used in the synthesis of hollow particles or binders (including but not limited to: water) , ethanol, isopropanol, toluene); inorganic acid catalysts used in the synthesis of binders (including but not limited to: hydrochloric acid, sulfuric acid, phosphoric acid), organic acid or anhydride catalysts (for example including but not limited to: acetic acid, acetic anhydride , citric acid), inorganic base catalyst (including but not limited to: ammonia, sodium hydroxide, potassium hydroxide), inorganic salt catalyst (for example including but not limited to: ammonium chloride, ammonium sulfate, sodium chloride, Sodium sulfate); a mineral acid catalyst (for example, including but not limited to: hydrochloric acid, sulfuric acid, phosphoric acid), an organic acid or an acid anhydride catalyst (for example, including but not limited to: acetic acid, acetic acid) used to form a chemical bond between the hollow particles and the binder. Anhydride, citric acid), inorganic base catalysts (including, but not limited to, ammonia, sodium hydroxide, potassium hydroxide), inorganic salt catalysts (including, but not limited to, ammonium chloride, ammonium sulfate, sodium chloride, sodium sulfate) ).

The present invention also provides a method of preparing an antireflective composition comprising (a) providing a hollow particle having a hydroxyl group on a surface thereof; (b) providing a binder having a group capable of forming a chemical bond with the hydroxyl group; (c) mixing the hollow particles with the binder to provide a mixture; and (d) optionally maintaining the temperature of the mixture at a temperature of from about 0 ° C to about 100 ° C in the presence of a desired catalyst and/or water, Make the hollow The hydroxyl group on the surface of the particle reacts with the group of the binder to form a chemical bond. Among them, the types and characteristics of the hollow particles and the binder which can be used in the method of the present invention are as described above.

The method suitable for providing the hollow particles is determined depending on the materials and kinds of the hollow particles, and is not particularly limited. According to an embodiment of the present invention, the hollow particles may be provided by providing a template which is a micelle formed of a polyelectrolyte; depositing a decane precursor on the template; and removing The template is obtained to obtain the hollow particles. Taking the hollow particles of cerium oxide as an example, a polyelectrolyte such as polyacrylic acid, sodium polyacrylate, polyacrylamine hydrochloride, and a polar solvent such as ethanol or isopropyl alcohol are mixed to form a micelle as a template, and reprecipitation is performed as a template. The decane precursor of acid methyl ester, ethyl orthosilicate, sodium citrate is on the template, and then the template is washed to remove hollow cerium oxide hollow particles. Further, as an example of providing an organic decane hollow particle, as described above, a procedure for providing cerium oxide hollow particles is used, except for using, for example, tetramethoxy decane, tetraethoxy decane (TEOS), methyl triethoxy decane, methyl The organosilsesquioxane of trimethoxydecane, vinyltrimethoxydecane, and phenyltriethoxydecane is used as a decane precursor.

In the method of the present invention, the particle size, particle size uniformity, and pore diameter of the hollow portion of the hollow particle can be controlled in the preparation process. For example, the size and uniformity of the formed micelles (templates) can be controlled by adjusting the molecular weight, the amount, and the dispersion rate of the polyelectrolyte, thereby controlling the porosity of the hollow portion of the obtained hollow particles; The size of the bundle (template) and the amount of the decane precursor control the particle size of the hollow particles provided.

Step (b) of the method of the present invention consists in providing a layer which can form with the hydroxyl group The bonding agent of the chemically bonded group, the step (b) differs depending on the kind of the binder; and as mentioned above, the binder which can be used in the present invention comprises an organic oxime resin, a modified organic oxime resin , inorganic cerium sol, or a combination of the foregoing.

In the case of providing an organic tantalum resin binder, water may be added to an alkyl decane having a chlorine atom (such as methyltrichloromethane or dimethyl ester in the presence of an organic solvent such as toluene and at a relatively low temperature. a chlorinated phenyl decane (such as phenyl trichloro decane, diphenyl chlorocycloalkane), an alkyl group having a chlorine atom, a chlorinated phenyl decane (such as phenyl trichloro decane) a phenyl decane (such as methyl phenyl dichloro decane, vinyl phenyl dichloro decane), or a mixture of the foregoing, which is reacted to obtain an acidic hydrolyzate, which is then subjected to a heating or a catalyst. The hydrolyzate is further polycondensed to form a highly crosslinked polyorganosiloxane having a network structure. The organic oxime resin binder can also be formed by reacting an alkyl alkane having an alkoxy group, a phenyl decane having an alkoxy group, or a mixture thereof with water in the presence of an acid or a non-acid catalyst. For example, methyltriethoxydecane is dissolved in ethanol and reacted with water under acid catalysis to polymerize into a transparent polymethyltriethoxysilsesquioxane resin. A mixture of vinyltriethoxydecane and phenyltriethoxydecane is reacted with water under acid catalysis to form a polyorganosilsesquioxane composite organic oxime resin. An MQ resin composed of a monofunctional chain link (R ₃ SiO _0.5 ) and a tetrafunctional chain link (SiO ₂ ) can be obtained by cohydrolysis polycondensation of tetraethoxynonane and hexamethyldioxane under acid catalysis. As for the modified organic oxime resin, such as an epoxy-modified organic oxime resin, a modifying group is usually used as a blocking or copolymer, and a hybrid organic oxime resin is formed with polysiloxane. Inorganic cerium sols, such as highly crosslinked cerium oxide sols, can be formed by hydrolysis under polycondensation of tetraethoxy decane under acid catalysis. Among them, the types of catalysts that can be used are as mentioned above.

The method of the invention then mixes the hollow particles with the binder to provide a mixture, an anti-reflective composition, step (c). After the step (c), the method of the present invention may further comprise a step (d) of maintaining the temperature of the mixture at a temperature of from about 0 ° C to about 100 ° C, preferably about 60 ° C, in the presence of a desired catalyst and/or water. Up to about 90 ° C, the hydroxyl group on the surface of the hollow particle is reacted with the group of the binder (such as -OH, -COOH, -CNH, -CONH-, -NCO, etc.) to form a chemical bond, especially as Covalent bonding of -O-, -COO-, and the like. Wherein, the kind of the catalyst which can be used is as mentioned above, for example, may be selected from the following groups (but not limited to): hydrochloric acid, sulfuric acid, phosphoric acid, acetic acid, acetic anhydride, citric acid, ammonia water, sodium hydroxide, hydrogen hydroxide. Potassium, ammonium chloride, ammonium sulfate, sodium chloride, sodium sulfate, and combinations of the foregoing.

According to an embodiment of the present invention, the antireflective composition can be prepared by the following steps: (a) providing a hollow particle having a hydroxyl group on a surface, and dispersing the hollow particle in a first solvent to provide a a first dispersion; wherein the first solvent is selected depending on the surface properties of the hollow particles, and may be a polar solvent such as water or an alcohol or a non-polar solvent such as toluene to form a uniform, stable, and dispersed solvent. a hollow particle dispersion is preferred; (b) providing a binder having a group capable of forming a chemical bond with the hydroxyl group, and dispersing the binder in a second solvent to provide a second dispersion; The second solvent is selected depending on the solubility of the binder and the solvent, and may be a polar solvent such as water or an alcohol or a non-polar solvent such as toluene to form a clear and transparent solution; (c) mixing The first dispersion and the second dispersion to provide the mixture; and (d) optionally maintaining the mixture in the presence of a desired catalyst and/or water The temperature of the compound is from about 0 ° C to about 100 ° C, preferably from about 60 ° C to about 90 ° C, such that the hydroxyl group on the surface of the hollow particle reacts with the group of the binder to form a chemical bond.

Other additives may be added before or during the above mixing step (c), including dispersing agents (such as polyacrylic acid, polyvinyl alcohol, polyethylene glycol, sodium benzoate); small molecule cosolvents (such as sodium salicylate, amines) Benzoic acid, urea, nicotinamide, acetaminophen); surfactants with solubilizing effects (such as Tween, Span), help to provide uniform, stable and transparent mixed dispersion body.

In the above mixing step (d), maintaining the temperature of the mixture in the presence of a catalyst and/or water at from about 60 ° C to about 90 ° C such that at least a portion of the hydroxyl groups on the surface of the hollow particles and at least a portion of the binder are present in the group The reaction forms a chemical bond. As used herein, "at least a portion of the hydroxyl group" means at least two or more hydroxyl groups, preferably from about 20% to about 100% hydroxyl groups, more preferably from about 40% to about 60%. a hydroxyl group; "at least a portion of the group" means at least two or more groups reactive with a hydroxyl group, preferably from about 20% to about 100% reactive with a hydroxyl group. The group, more preferably from about 40% to about 60% of the groups reactive with the hydroxyl group, can be tailored to the desired properties or optical properties of the antireflective film.

The present invention also provides an antireflective sheet, generally comprising a substrate, and at least one surface of the substrate has at least one film formed from the antireflective composition as described above. The anti-reflective film is composed of hollow particles and a binder, and the hollow particles can be formed in a single layer arrangement in the film, or can be formed in a multi-layer arrangement depending on the requirements. As shown in the appended examples, the films provided by the present invention have a relatively low refractive index (about 1.2 to 1.3), exhibit excellent abrasion resistance, scratch resistance, and provide improved adhesion.

The substrate suitable for the antireflection sheet of the present invention may be selected according to practical applications, and may include, but not limited to, a glass substrate, a ruthenium substrate, a polymer substrate (such as a polymethyl methacrylate substrate, polycarbonate). Ester substrate, polyethylene terephthalate substrate).

For example, the anti-reflective composition of the present invention can be applied to at least one surface of a substrate to form at least one coating, and then dried by heating to form an excellent abrasion resistance and scratch resistance and a low refractive index. The film can be used as an antireflection film. The above methods of administration may be any of those of ordinary skill in the art to which the present invention pertains, and may generally include, but are not limited to, a screen-printing method, a coating method, or a dispensing method. Wherein, the coating method includes, for example, knife coating, roller coating, micro gravure coating, flow coating, dip coating, Spray coating, curtain coating, or a combination of the above.

In the present invention, the step of forming a chemical bond between the hydroxyl group on the surface of the hollow particle and the group of the binder can be carried out according to the process convenience and the needs of the user. For example, this step can be carried out after mixing the hollow particles with the binder, before applying to the substrate, or after application to the substrate.

The antireflective sheet of the present invention is particularly useful for displays, optical lenses, polarizing films, and solar cell panels, as well as for other applications found in the art.

The invention is further illustrated by the following specific examples, which are not intended to limit the scope of the invention in any way.

Example [Preparation of hollow particles of the present invention] Preparation Example 1

Approximately 0.08 grams of polyacrylic acid having an average molecular weight of about 5,000 was mixed with about 1.5 ml of 25% aqueous ammonia to completely dissolve, added to about 30 ml of absolute ethanol, and stirred at about 900 rpm for about 30 minutes to obtain a pale blue. Color sol. About 0.5 ml of tetraethoxysilane was added to the pale blue sol, and after stirring for about 4 hours, the obtained product was diluted with deionized water, and washed repeatedly with an ultrafiltration membrane to obtain hollow particles.

[Preparation of hollow particles modified with a hydrocarbon-containing decane coupling agent] Preparation Example 2

Approximately 0.08 grams of polyacrylic acid having an average molecular weight of about 5,000 was mixed with about 1.5 ml of 25% aqueous ammonia to completely dissolve, added to about 30 ml of absolute ethanol, and stirred at about 900 rpm for about 30 minutes to obtain a pale blue. Color sol. About 0.5 ml of tetraethoxy decane was added to the pale blue sol, and after stirring for about 4 hours, the obtained product was diluted with deionized water, washed repeatedly with an ultrafiltration membrane, and dispersed in methanol to obtain hollow particles. Methanol sol. Next, a final concentration of about 28% ammonia water is added to about 100 grams of about 20% by weight of the hollow nanoparticle methanol sol. After thorough mixing, the concentration is adjusted to about 400 ppm, and about 4 grams of methacrylonitrile is added.矽 ( ( purchased from Confidence Chemical Co., Ltd., KBM503), mixed uniformly, heated to about 50 ° C for about 15 hours, cooled to room temperature, filtered through an ultrafiltration membrane, and washed repeatedly to obtain modified hollow particles. .

[testing method]

The various properties of the hollow particles of Preparation Example 1 and Preparation Example 2 were analyzed in the following manner.

(A) Topography

About 1 ml of the hollow particle sol was dropped on a copper mesh, and after drying, the morphology of the particles was analyzed by a transmission electron microscope (purchased from JEOL Co., Ltd., JEOL 1011).

(B) particle size distribution, average particle size, and polydispersity coefficient

The hollow particle sol was diluted to about 0.5% by weight, and the particle size distribution curve, the volume average particle diameter, and the volume were measured by a laser dynamic light scattering method using a particle size distribution measuring device (Malvern Nano ZS, measuring principle of dynamic light scattering method). The average particle diameter (Dv), the number average particle diameter (Dn), and the polydispersity coefficient (Dv/Dn) were calculated.

(C) Average pore size and pore size distribution

About 100 ml of the hollow particle sol was dried at about 60 ° C for about 48 hours, and the average pore size and pore size distribution of the obtained sample were analyzed by a surface area and porosity analyzer ASAP2020 (Micromeritics Instrument Corporation).

(D) surface hydroxyl group

About 100 ml of the hollow particle sol was dried at about 60 ° C for about 48 hours, and the obtained sample was placed in a Fourier transform infrared spectrometer (Nicolet 380 FT-IR) to detect the powder sample of the head and the machine after extrusion drying. Infrared spectroscopy.

(E) surface hydroxyl density

Determine the hydroxyl density of the surface of the nanoparticle by titration. The specific steps are as follows: Weigh about 1 gram of dried hollow nanoparticle sample and place it in a 250 ml iodine measuring flask, add about 10 ml of toluene and mix well; add about 25 0.5 ml/ml of 2,4-toluene diisocyanate toluene solution and 1 ml of 1% N,N-dimethylcyclohexylamine toluene solution, thoroughly mixed and left for about 10 minutes; then, add about 25 ml 1 mol/L of diethylamine toluene solution, mix well and leave for about 10 minutes; add about 20 ml of isopropanol and 1 to 2 drops of bromocresol green indicator solution were titrated with a 0.5 mol/liter hydrochloric acid standard solution until the blue color became yellow, and the volume of the hydrochloric acid standard solution consumed was measured.

Calculate the percentage of hydroxyl in the sample according to the formula 0.01701×C(V1-V0)/m, where m is the mass of the sample (g); C is the concentration of the standard solution of hydrochloric acid (mole/liter); V1 is the consumption of the sample The volume of the hydrochloric acid standard solution (ml); V0 is the volume (ml) of the hydrochloric acid standard solution consumed by the control sample (blank).

Fig. 1 is a transmission electron micrograph of the hollow particles of Preparation Example 1, showing that the obtained particles were spherical and had a hollow structure.

Fig. 2 is a particle size distribution of the hollow particles of Preparation Example 1. From the calculation results, it was found that the obtained hollow particles had a number average particle diameter (Dn) of 57.5 nm, a volume average particle diameter (Dv) of 58.6 nm, and a polydispersion coefficient. (Dv/Dn) was 1.02, less than 1.05, indicating that the particle size was very uniform.

Fig. 3 is a view showing the pore size distribution of the hollow particles of Preparation Example 1, and the average pore diameter of the hollow portion of the obtained nanoparticles was 24.5 nm.

Fig. 4 is a FT-IR spectrum chart of the hollow particles of Preparation Example 1 and Preparation Example 2, wherein 3390 cm ^-1 to 3200 cm ^-1 and 910 cm ^-1 to 830 cm ^-1 are characteristic peaks of Si-OH. The FT-IR spectrum shows that the hollow nanoparticles of Preparation Example 1 and Preparation Example 2 all contain hydroxyl groups, but the data of Preparation Example 2 shows that the hydroxyl group has a weak peak of the hydroxyl group, indicating that the hydroxyl density of the surface of the hollow particles after chemical modification is Significant decline.

Table 1 shows the hydroxyl groups on the surface of the hollow particles of Preparation Example 1 and Preparation Example 2, which are shown as being surface-modified with respect to the hydrocarbon-containing decane coupling agent of Preparation Example 2 as compared with Preparation Example 1. The hollow particles have a reduced hydroxyl content.

[Preparation of anti-reflective composition] Example 1

About 7 grams of epoxy-modified organic hydrazine resin was dissolved in about 30 ml of xylene, and mixed with about 100 ml of 5% by weight of the hollow particle ethanol dispersion of Preparation 1, and about 5 ml of 1 molar concentration of HCl was added. The solution was distilled under reduced pressure at about 80 ° C for about 5 hours.

Example 2

Approximately 6 g of a polyorganosilsesquioxane resin obtained by cohydrolysis of methyltrimethoxydecane with vinyltriethoxydecane under acid catalysis is dissolved in about 30 ml of isopropanol, and about 100 ml. 5 wt% of the hollow particle isopropyl alcohol dispersion of Preparation Example 1 was mixed, and about 6 ml of a 1 molar solution of HCl was added thereto, and distilled under reduced pressure at about 80 ° C for about 8 hours.

Fig. 5 is a FT-IR spectrum of the reaction product of Example 2, and a characteristic peak of Si-O-Si in the vicinity of 1110 cm ^-1 indicates that the binder is present alone (i.e., polyorgano-silsesquioxane resin, PSQ) has a weaker transmission peak around 1110 cm ^-1 , and the resulting product becomes stronger at a peak of 1110 cm ^-1 when the binder reacts with the hollow nanoparticles under acid catalysis for a period of time. This indicates that the binder itself contains a certain amount of Si-O-Si covalent bond, and forms more Si-O-Si covalent bonds after reacting with the hollow particles under acid catalysis for a period of time.

Example 3

About 8 grams of MQ resin was dissolved in about 20 ml of toluene, and mixed with about 100 ml of 5% by weight of the hollow nanoparticle isopropyl alcohol dispersion of Preparation Example 1, and about 2 ml of 1 molar concentration of H ₂ SO was added. _The solution was distilled under reduced pressure at about 90 ° C for about 8 hours.

Comparative example 1

The hollow particles of Preparation Example 2 were replaced with about 100 ml of ethanol solution, and mixed with about 30 ml of a xylene solution containing about 7 g of epoxy-modified organic hydrazine resin, and about 5 ml of a 1 molar concentration of HCl solution was added. It was distilled under reduced pressure at about 80 ° C for about 5 hours.

Comparative example 2

The hollow particles of Preparation Example 2 were replaced with about 100 ml of an isopropanol solution, and about 30 ml of a polyorganic organic compound obtained by cohydrolysis of about 6 g of methyltrimethoxydecane with vinyltriethoxydecane under acid catalysis. The isopropanol solution of the sesquisesquioxane resin was uniformly mixed, and about 6 ml of a 1 molar solution of HCl was added thereto, and the mixture was distilled under reduced pressure at about 80 ° C for about 8 hours.

Comparative example 3

The hollow particle dispersion of Preparation Example 2 was replaced with about 100 ml of an isopropanol solution, and mixed with about 30 ml of a toluene solution containing about 8 g of MQ resin, and about 2 ml of a 1 molar concentration of H ₂ SO ₄ solution was added. It was distilled under reduced pressure at about 90 ° C for about 8 hours.

[Production of anti-reflection sheet]

About 100 g of the products obtained in the above Examples 1 to 3 and Comparative Examples 1 to 3 were respectively taken as an antireflection composition, and the glass substrate was immersed in the antireflection composition at a rate of about 5 minutes/second, and immersed for about 5 seconds. Thereafter, the glass substrate was taken out at the same speed and dried at about 500 ° C for about 1 hour to form films I, II and III and comparative films IV, V and VI.

[testing method]

The adhesion of the films I, II and III to the comparative films IV, V and VI, the pencil hardness, the scratch resistance, the refractive index, the light transmittance at a wavelength of about 550 nm, and the reflectance were measured in the following manner. .

(F) Adhesion

11 parallel scratches were drawn in the horizontal and vertical directions by a knife on the surface of the film on the glass substrate at intervals of 1 mm to form 100 squares. After bonding with tape (3M), the tape was peeled off from the film. The number of remaining lattices was evaluated for adhesion according to the following criteria.

A: The number of residual squares is 95 or more; B: the number of residual squares is 90-94; C: the number of residual squares is 85-89; and D: the number of residual squares is 84 or less.

(G) pencil hardness

Pencil hardness was measured with a pencil hardness tester, and pencils of different hardness (8H, 7H, 6H, 5H) were attached at an angle of about 45 degrees to the surface of the film on the substrate. After loading a certain weight, the pencil was stretched at a certain speed to observe the presence or absence of Scratches.

(H) Scratch resistance

The surface of the film on the substrate was slid 10 times under a load of about 250 g using 0000# steel wool, and the surface of the coating was visually observed and evaluated according to the following criteria.

AA: no streaky scratches; BB: slightly striped scratches; CC: a large number of striped scratches; and DD: overall surface shedding.

(I) refractive index

The refractive index of the film on the substrate was analyzed with an ellipsometer (available from J.A. Woollam, Inc., M-2000V).

(J) Transmittance and reflectivity

The transmittance of the film on the substrate at a wavelength of about 550 nm was measured by an ultraviolet-visible spectrophotometer (Lambda 950); and the reflectance was measured by an ultraviolet-visible spectrophotometer (Lambda 950). The blank glass substrate has a light transmittance of about 91.76% and a reflectance of about 8.2% at a wavelength of about 550 nm.

The results of the test methods (F) to (J) are shown in Table 2.

The results in Table 2 show that the films (films I to III) formed by the antireflection composition of the present invention have better density than the films containing the surface-modified hollow nanoparticles (Comparative Films IV to VI). Significant, large pencil hardness, better scratch resistance. Meanwhile, the films I to III of the present invention have a desired low refractive index, high light transmittance, and low reflectance.

The above embodiments are merely illustrative of the principles and effects of the present invention, and are illustrative of the technical features of the present invention and are not intended to limit the scope of the present invention. Any changes or arrangements that can be easily accomplished by those skilled in the art without departing from the technical principles and spirit of the invention are within the scope of the invention. Accordingly, the scope of the invention is set forth in the appended claims.

1 is a transmission electron micrograph of the hollow particles of Preparation Example 1; and FIG. 2 is a particle size distribution diagram, a numerical average particle diameter (Dn), and a polydispersity coefficient (Dv/Dn) of the hollow particles of Preparation Example 1. ); 3 is an average pore size and pore size distribution diagram of the hollow particles of Preparation Example 1; FIG. 4 is a Fourier-converted infrared spectrum of hollow nanoparticles of Preparation Examples 1 and 2; and FIG. 5 is an implementation The Fourier transform infrared spectrum of the antireflective composition formed by the reaction of the hollow particles of Example 2 with a binder.

Claims (13)

An antireflection composition comprising: hollow particles having a hydroxyl group on a surface, having an average particle diameter of from 10 nm to 200 nm and a porosity of a hollow portion of from 10% to 90%, and a density of the hydroxyl group More than 2%; and a binder having a group capable of forming a chemical bond with the hydroxyl group. The composition of claim 1, wherein the material of the hollow particles is selected from the group consisting of cerium oxide, organic decane, and combinations of the foregoing. The composition of claim 1, wherein the hollow particles have an average particle diameter of from 20 nm to 100 nm and a porosity of from 20% to 80%. The composition of claim 1, wherein the particle size of the hollow particles has a polydispersity coefficient (Dv/Dn) of less than 1.05. The composition of claim 1, wherein the hollow particle has a spherical shape, an ellipsoid shape, or a peanut shape. The composition of claim 1, wherein the binder is selected from the group consisting of an organic resin, a modified organic resin, an inorganic sol, and combinations thereof. The composition of claim 1, wherein the group capable of forming a chemical bond with the hydroxyl group is selected from the group consisting of -OH, -COOH, -CNH, -CONH, -NCO, and combinations of the foregoing. The composition of claim 1, wherein the hollow particles are contained in an amount of from 1 part by weight to 20 parts by weight per 100 parts by weight of the binder. A method of preparing an antireflective composition comprising: (a) providing a hollow particle having a hydroxyl group on a surface; (b) providing a binder having a group capable of forming a chemical bond with the hydroxyl group; (c) Mixing the hollow particles with the binder to provide a mixture; and (d) optionally maintaining the temperature of the mixture at 0 ° C to 100 ° C in the presence of a desired catalyst and/or water to surface the hollow particles The hydroxyl group reacts with the group of the binder to form a chemical bond. The method of claim 9, comprising: (a) providing a hollow particle having a hydroxyl group on the surface, and dispersing the hollow particle in a first solvent to provide a first dispersion; (b) providing a bond And a group capable of forming a chemical bond with the hydroxyl group, and dispersing the binder in a second solvent to provide a second dispersion; (c) mixing the first dispersion and the second dispersion To provide the mixture; and (d) optionally maintaining the mixture at a temperature between 0 ° C and 100 ° C in the presence of a desired catalyst and/or in the presence of the hydroxyl group on the surface of the hollow particle and the binder This group reacts to form a chemical bond. The method of claim 9 or 10, wherein in the step (a), the hollow particles are provided by providing a template which is a micelle formed of a polyelectrolyte; and precipitating a decane precursor to the template And removing the template to obtain the hollow particles. The method of claim 9 or 10, wherein the step (d) is at 60 ° C to 90 ° C The temperature is carried out, and the catalyst is selected from the group consisting of hydrochloric acid, sulfuric acid, phosphoric acid, acetic acid, acetic anhydride, citric acid, ammonia, sodium hydroxide, potassium hydroxide, ammonium chloride, ammonium sulfate, sodium chloride, Sodium sulfate, and combinations of the foregoing. An antireflection sheet comprising a substrate, and at least one surface of the substrate has at least one film formed of the antireflective composition of claim 1.