Anti-reflective coating composition including siloxane compound, and anti-reflective film of which surface energy is adjusted using same

Abstract

The present invention relates to an anti-reflective coating composition, to an anti-reflective film using same, and to a method for preparing the anti-reflective film, wherein the anti-reflective coating composition is capable of forming a coating layer that has a low refractive index and adjusting the surface energy. More particularly, the present invention relates to an anti-reflective film of which the reflectance is minimized and the surface energy is adjusted, by forming a coating layer using an anti-reflective coating composition that contains, as a binder, a siloxane compound which is synthesized by reacting organosilane that has a fluroalky group with alkoxysilane at a certain weight ratio, and also relates to a method for preparing the anti-reflective film. The anti-reflective film using the anti-reflective coating composition has excellent anti-reflective performance, and is thus expected to be applicable to various display devices such as a touch film.

Claims

1. An anti-reflective coating composition comprising: a binder formed by polymerization of 100 parts by weight of a silane compound represented by Formula 1 and 5 parts by weight to 10 parts by weight of an organosilane compound represented by Formula 2; a pH control agent; and hollow silica particles, wherein the pH control agent includes one selected from the group consisting of ammonia, organic amines, metal hydroxide solution and a combination thereof, wherein the composition has a pH of 3 to 8, wherein the binder is a siloxane compound having a weight-averaged molecular weight of 1,000 to 100,000,
R.sup.1.sub.xSi(OR.sup.2).sub.4x[Formula 1] wherein R.sup.1 is a C.sub.1 to C.sub.10 alkyl group, a C.sub.6 to C.sub.10 aryl group or a C.sub.3 to C.sub.10 alkenyl group, R.sup.2 is a C.sub.1 to C.sub.6 alkyl group, and x is an integer satisfying 0x<4,
R.sup.3.sub.ySi(OR.sup.4).sub.4y[Formula 2] wherein R.sup.3 is a C.sub.1 to C.sub.12 fluoroalkyl group, R.sup.4 is a C.sub.1 to C.sub.6 alkyl group, and y is an integer satisfying 0x<4.

2. The coating composition according to claim 1, wherein the silane compound represented by Formula 1 comprises at least one compound selected from among tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetraisopropoxysilane, tetra-n-butoxysilane, tetra-sec-butoxysilane, tetra-tert-butoxysilane, trimethoxysilane, triethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, isobutyltriethoxysilane, cyclohexyltrimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, allyltrimethoxysilane allyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, diphenyldimethoxysilane, and diphenyldiethoxysilane.

3. The coating composition according to claim 1, wherein the organosilane compound represented by Formula 2 comprises at least one compound selected from among trifluoromethyltrimethoxysilane, trifluoromethyltriethoxysilane, trifluoropropyltrimethoxysilane, trifluoropropyltriethoxysilane, nonafluorobutylethyltrimethoxysilane, nonafluorobutylethyltriethoxysilane, nonafluorohexyltrimethoxysilane, nonafluorohexyltriethoxysilane, tridecafluorooctyltrimethoxysilane, tridecafluorooctyltriethoxysilane, heptadecafluorodecyltrimethoxysilane, and heptadecafluorodecyltriethoxysilane.

4. The coating composition according to claim 1, wherein x in Formula 1 is an integer of 0, 1, or 2.

5. The coating composition according to claim 1, wherein R.sup.3 in Formula 2 is a C.sub.3 to C.sub.5 fluoroalkyl group.

6. The coating composition according to claim 1, wherein the hollow silica particles have a number average diameter of 1 nm to 1,000 nm.

7. The anti-reflective coating composition according to claim 1, further comprising: a particle dispersion medium.

8. The anti-reflective coating composition according to claim 7, the particle dispersion medium comprises one or more of water or an organic solvent.

9. The anti-reflective coating composition according to claim 7, wherein a content of the hollow silica particles dispersed in the particle dispersion medium is 5% by weight to 40% by weight.

10. An anti-reflective film including a coating layer formed on a surface of a substrate comprising the anti-reflective coating composition according to claim 1, wherein the coating layer has a water contact angle of 40 to 80 on the surface thereof, wherein the coating layer has an index of refraction of 1.20 to 1.25.

11. The anti-reflective film according to claim 10, wherein the coating layer has a thickness of 1 nm to 1,000 nm.

12. The anti-reflective film according to claim 10, wherein the anti-reflective film has a transmittance of 94% or more and a luminous reflectance of 0.5% to 2.0%.

13. A touch panel comprising the anti-reflective film according to claim 10.

14. A method for manufacturing an anti-reflective film, comprising: preparing a binder by polymerization of 100 parts by weight of a silane compound represented by Formula 1 and 5 parts by weight to 10 parts by weight of an organosilane compound represented by Formula 2; preparing a coating composition comprising surface-treated hollow silica particles by adding the binder, a pH control agent and an acid catalyst to hollow silica particles, and adjusting the coating composition to a pH of 3 to 8; coating the coating composition onto at least one surface of a base film; and performing heat treatment of the coated coating composition, wherein the pH control agent includes one selected from the group consisting of ammonia, organic amines, metal hydroxide solution and a combination thereof, wherein the binder is a siloxane compound having a weight-averaged molecular weight of 1,000 to 100,000,
R.sup.1.sub.xSi(OR.sup.2).sub.4x[Formula 1] wherein R.sup.1 is a C.sub.1 to C.sub.10 alkyl group, a C.sub.6 to C.sub.10 aryl group or a C.sub.3 to C.sub.10 alkenyl group, R.sup.2 is a C.sub.1 to C.sub.6 alkyl group, and x is an integer satisfying 0x<4,
R.sup.3.sub.ySi(OR.sup.4).sub.4y[Formula 2] wherein R.sup.3 is a C.sub.1 to C.sub.12 fluoroalkyl group, R.sup.4 is a C.sub.1 to C.sub.6 alkyl group, and y is an integer satisfying 0x<4.

15. The method according to claim 14, wherein the coating composition is prepared by adding the binder and the acid catalyst to the hollow silica particles, followed by stirring at 20 C. to 40 C. for 5 hours to 50 hours.

16. The method according to claim 14, wherein heat treatment is performed at a temperature of 50 C. to 200 C.

Description

BEST MODE

(1) The above and other aspects, features, and advantages of the present invention will become apparent from the detailed description of the following embodiments in conjunction with the accompanying drawings. However, it should be understood that the present invention is not limited to the following embodiments and may be embodied in different ways, and that the embodiments are provided for complete disclosure and thorough understanding of the invention by those skilled in the art. The scope of the invention should be defined only by the accompanying claims and equivalents thereof.

(2) Hereinafter, an anti-reflective coating composition, an anti-reflective film and a method for manufacturing the anti-reflective film according to the present invention will be described in detail.

(3) Anti-Reflective Coating Composition

(4) In accordance with one aspect of the present invention, an anti-reflective coating composition includes: a binder formed by polymerization of 100 parts by weight of a silane compound represented by Formula 1 and 0.1 parts by weight to 20 parts by weight of an organosilane compound represented by Formula 2; and hollow silica particles.
R.sup.1.sub.xSi(OR.sup.2).sub.4x[Formula 1]

(5) wherein R.sup.1 is a C.sub.1 to C.sub.10 alkyl group, a C.sub.6 to C.sub.10 aryl group or a C.sub.3 to C.sub.10 alkenyl group, R.sup.2 is a C.sub.1 to C.sub.6 alkyl group, and x is an integer satisfying 0x<4.
R.sup.3.sub.ySi(OR.sup.4).sub.4y[Formula 2]

(6) wherein R.sup.3 is a C.sub.1 to C.sub.12 fluoroalkyl group, R.sup.4 is a C.sub.1 to C.sub.6 alkyl group, and y is an integer satisfying 0x<4.

(7) The anti-reflective coating composition has a lower index of refraction and thus exhibits improved anti-reflection. Since the hollow silica particles have a low index of refraction due to a hollow structure therein, a layer realizing a low index of refraction can be formed from the hollow silica-containing anti-reflective coating composition. Generally, a fluorine-containing coating composition is used to reduce an index of refraction. In this case, there can be a problem of reduction in adhesion, which is required upon formation of a layer in a stack structure, due to reduction in surface energy. On the other hand, the anti-reflective coating composition as set forth above can form a layer which has relatively high surface energy while realizing a low index of refraction. The anti-reflective coating composition includes the silane compound represented by Formula 1 and the organosilane compound represented by Formula 2 in the content ratio as set forth above, thereby allowing surface energy not to be reduced while realizing a low index of refraction.

(8) The silane compound represented by Formula 1 may be a tetrafunctional alkoxy silane having four alkoxy groups when x is 0; a trifunctional alkoxy silane having three alkoxy groups when x is 1; and a bifunctional alkoxy silane having two alkoxy groups when x is 2. The silane compound represented by Formula 1 when x is 3 is not advantageous in condensation with the organosilane compound represented by Formula 2 since the silane compound has only one alkoxy group which is a functional group.

(9) In Formula 1, the C.sub.6 to C.sub.10 aryl group may include a phenyl group, a tolyl group and the like, and the C.sub.3 to C.sub.10 alkenyl group may include an allyl group, a 1-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group and the like.

(10) The silane compound may include at least one compound selected from among tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetraisopropoxysilane, tetra-n-butoxysilane, tetra-sec-butoxysilane, tetra-tert-butoxysilane, trimethoxysilane, triethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, isobutyltriethoxysilane, cyclohexyltrimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, allyltrimethoxysilane allyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, diphenyldimethoxysilane, and diphenyldiethoxysilane, without being limited thereto.

(11) In addition, the organosilane compound represented by Formula 2 may include at least one compound selected from among trifluoromethyltrimethoxysilane, trifluoromethyltriethoxysilane, trifluoropropyltrimethoxysilane, trifluoropropyltriethoxysilane, nonafluorobutylethyltrimethoxysilane, nonafluorobutylethyltriethoxysilane, nonafluorohexyltrimethoxysilane, nonafluorohexyltriethoxysilane, tridecafluorooctyltrimethoxysilane, tridecafluorooctyltriethoxysilane, heptadecafluorodecyltrimethoxysilane, and heptadecafluorodecyltriethoxysilane, without being limited thereto. In addition, it is advantageous that R.sup.3 is a C.sub.3 to C.sub.5 fluoroalkyl group in terms of prevention of phase separation. A siloxane compound is formed by hydrolysis and dehydration condensation polymerization of the silane compound represented by Formula 1 and the organosilane compound represented by Formula 2. In hydrolysis and dehydration condensation polymerization, an acid catalyst may be used. Specifically, nitric acid, hydrochloric acid, sulfuric acid, acetic acid or the like may be used.

(12) In polymerization, the organosilane compound represented by Formula 2 is used in an amount of 0.1 parts by weight to 20 parts by weight, preferably 1 part by weight to 15 parts by weight, more preferably 5 parts by weight to 10 parts by weight, based on 100 parts by weight of the silane compound represented by Formula 1. If the amount of the organosilane compound is less than 0.1 parts by weight, there are problems in that a formed coating layer has an excessively low contact angle and provides insignificant reduction in index of refraction, and if the amount of the organosilane compound is greater than 20 parts by weight, there are problems in that the coating layer can have an excessively large contact angle and an increased index of refraction. Thus, the amount of the organosilane compound represented by Formula 2 may be adjusted within the range as set forth the above depending upon a required water contact angle.

(13) The formed siloxane compound acts as an organic-inorganic hybrid binder and thus serves to treat a surface of the hollow silica particles. As such, if the hollow silica particles are subjected to surface treatment with the binder, the coating layer can have a further reduced index of refraction.

(14) The siloxane compound has a weight average molecular weight of 1,000 to 100,000, preferably 2,000 to 50,000, more preferably 5,000 to 20,000. If the weight average molecular weight is less than 1,000, it is difficult to form a coating layer having a desired low index of refraction, and if the weight average molecular weight is greater than 100,000, there is a problem of deterioration in light transmittance of an anti-reflective film.

(15) The hollow silica particles refer to silica particles which are derived from a silicon compound or an organic silicon compound and have an empty space on a surface thereof and/or therein. As described above, since the hollow silica particles have an empty space therein, the coating layer can realize a lower index of refraction.

(16) The hollow silica particles may be dispersed in a dispersion medium (water or organic solvent) to form a colloid having a solid content of 5% by weight (wt %) to 40 wt %. Here, an organic solvent capable of being used as the dispersion medium may include: alcohols such as methanol, isopropyl alcohol (IPA), ethylene glycol, butanol, and the like; ketones such as methyl ethyl ketone, methyl isobutyl ketone (MIBK), and the like; aromatic hydrocarbons such as toluene, xylene, and the like; amides such as dimethyl formamide, dimethyl acetamide, N-methyl pyrrolidone, and the like; esters such as ethyl acetate, butyl acetate, -butyrolactone, and the like; ethers such as tetrahydrofuran, 1,4-dioxane, and the like; and mixtures thereof. However, when a colloid solution in which the hollow silica particles are dispersed in a dispersion medium is used, it is desirable that the amount of the hollow silica be adjusted within the range as set forth above in consideration of solid content and the like.

(17) In addition, it is advantageous in maintenance of transparency of a film and in exhibition of anti-reflection thereof that the hollow silica particles have a number average diameter of 1 nm to 1,000 nm, preferably 5 nm to 500 nm, more preferably 10 nm to 100 nm.

(18) The binder of the siloxane compound is present in an amount of 10 parts by weight to 120 parts by weight, preferably 20 parts by weight to 100 parts by weight, more preferably 40 parts by weight to 80 parts by weight, based on 100 parts by weight of the hollow silica particles. If the amount of the binder is less than 10 parts by weight, there is a problem of whitening of a coating surface, and if the amount of the binder is greater than 120 parts by weight, there is a problem of significant deterioration in anti-reflection of the coating layer.

(19) The coating composition may include an acid catalyst to promote surface treatment of the hollow silica particles with the binder, and the acid catalyst may be any acid catalyst generally used in the art without limitation. Preferably, the acid catalyst is nitric acid or hydrochloric acid. The acid catalyst may be present in an amount of 0.1 parts by weight to 20 parts by weight based on 100 parts by weight of the hollow silica particles.

(20) In manufacture of the anti-reflective coating composition, it is advantageous that the coating composition have a pH of 2 to 9, preferably 3 to 8, more preferably 4 to 7 in terms of adjustment of contact angle.

(21) The anti-reflective coating composition may further include a pH control agent for pH control thereof. If OH.sup. ions in the composition are increased due to the pH control agent, a water contact angle of the composition can be reduced. The pH control agent may include ammonia, organic amines, metal hydroxide (LiOH, KOH, NaOH) solutions, and the like.

(22) Anti-Reflective Film

(23) In accordance with another aspect of the present invention, there is provided an anti-reflective film formed by coating the anti-reflective coating composition as set forth above onto a surface of a substrate.

(24) The substrate may include various substrates, such as transparent polymer resins and the like, used for typical liquid crystal displays and the like. Specifically, the substrate may include polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polyethersulfone (PES), polycarbonate (PC), polypropylene (PP), norbornene resins, and the like.

(25) When a material of the substrate is PET, a PET film has a thickness of about 10 m to about 200 m, preferably about 20 m to about 100 m. If the thickness of the transparent substrate is less than about 10 m, the substrate has a problem in mechanical strength, and if the thickness of the transparent substrate is greater than about 200 m, there is a possibility that the substrate does not exhibit improved touch properties as a substrate for touch panels.

(26) The coating layer formed of the anti-reflective coating composition may have a water contact angle of 40 to 80 on a surface thereof. If the water contact angle is less than 40, a protective film and the like are not separated well from the coating layer and the coating layer has a problem in terms of anti-contamination, and if the water contact angle is greater than 80, it is difficult to apply the coating layer to touch panels and the like due to problems in terms of adhesion of the surface of the coating layer.

(27) In addition, the coating layer formed of the anti-reflective coating composition has an index of refraction of 1.20 to 1.25.

(28) Further, the coating layer has a thickness of 1 nm to 1,000 nm, preferably 10 nm to 500 nm. If the thickness is less than 1 nm, there is a problem of insignificant anti-reflection of the coating layer, and if the thickness is greater than 1,000 nm, there is a problem of deterioration in adhesion of the coating layer.

(29) According to the present invention, the anti-reflective film has a transmittance of 94% or more and a luminous reflectance of 0.5% to 2.0%, and thus can exhibit excellent anti-reflection.

(30) Method for Manufacturing Anti-Reflective Film

(31) In accordance with a further aspect of the present invention, a method for manufacturing an anti-reflective film includes: preparing a binder by polymerization of 100 parts by weight of a silane compound represented by Formula 1 and 0.1 parts by weight to 20 parts by weight of an organosilane compound represented by Formula 2; preparing a coating composition including surface-treated hollow silica particles by adding the binder and an acid catalyst to hollow silica particles; coating the coating composition onto at least one surface of a base film; and performing heat treatment of the coated coating composition.

(32) The binder may be prepared as a siloxane compound by mixing 0.1 parts by weight to 20 parts by weight of the organosilane compound represented by Formula 2 with 100 parts by weight of the silane compound represented by Formula 1 in the presence of an acid catalyst, followed by dehydration and polymerization.

(33) The prepared binder is mixed with the hollow silica particles in a solvent in the presence of the acid catalyst, and used in surface treatment of the hollow silica particles. As such, the hollow silica particles are subjected to surface treatment, whereby the anti-reflective film can have a further reduced index of refraction. The binder and the hollow silica particles are mixed at 20 C. to 40 C. for about 5 hours to about 50 hours, preferably 10 hours to 40 hours, more preferably 20 hours to 30 hours while stirred.

(34) As described above, the coating composition may include 10 parts by weight to 120 parts by weight of the binder and 0.1 parts by weight to 20 parts by weight of the acid catalyst, based on 100 parts by weight of the hollow silica particles.

(35) In addition, in preparation of the coating composition, the coating composition is controlled to a pH of 2 to 9, preferably 3 to 8, more preferably 4 to 7. Further, a pH control agent and the like may be used for pH control of the coating composition, and the pH control agent may include ammonia, organic amines, metal hydroxide (LiOH, KOH, NaOH) solutions and the like.

(36) The coating composition obtained through mixing as set forth above is coated onto the at least one surface of the base film. Here, coating may be performed by one method selected from among gravure coating, slot die coating, spin coating, spray coating, bar coating, and dip coating, without being limited thereto.

(37) The coating composition may be coated to a thickness of 1 nm to 1,000 nm onto the one surface of the base film, followed by heat treatment at 50 C. to 200 C., thereby forming an anti-reflective layer. Specifically, the coated coating composition may be dried at a high temperature of 100 C. to 200 C. for about 1 minute to about 10 minutes to remove the solvent, followed by aging at 50 C. to 100 C. for about 10 hours to 100 hours, thereby forming the anti-reflective layer.

(38) Hereinafter, the present invention will be explained in more detail with reference to some examples.

(39) It should be understood that these examples are provided for illustration only and are not to be construed in any way as limiting the present invention.

EXAMPLE 1

(40) 1. Preparation of Siloxane Compound Binder

(41) 26 parts by weight of water, 290 parts by weight of isopropanol and 9 parts by weight of 0.1 M HNO.sub.3 were placed in a reactor, followed by stirring for 10 minutes. Next, 100 parts by weight of tetraethoxysilane (tetraethyl orthosilicate, TEOS) and 0.65 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane were slowly introduced into the reactor through a funnel for 30 minutes. Next, the components were stirred at 50 C. for 2 hours, followed by cooling to room temperature, and then stirred again at a speed of 200 rpm for 24 hours, thereby obtaining a transparent binder solution. It was confirmed that the solution had a solid content of 6.7 wt % and a pH of 2.1. The transparent solution was used in manufacture of a coating composition in the following stage without a separate purification process.

(42) 2. Preparation of Anti-Reflective Coating Composition

(43) 100 parts by weight of the prepared binder solution, 60 parts by weight of a hollow silica particle-methyl isobutyl ketone dispersion sol (Thrulya 4320, JGC C&C Co., Ltd., 20% w/w) having a number average diameter of 60 nm and 1 part by weight of NH.sub.4OH were placed in a reactor, followed by stirring at room temperature for 24 hours, thereby preparing an anti-reflective coating composition. It was confirmed that the prepared anti-reflective coating composition had a solid content of 3 wt % and a pH of 4.2.

(44) 3. Manufacture of Anti-Reflective Film

(45) The prepared anti-reflective coating composition was coated to a thickness of 100 nm onto a 20 m thick PET film using a Mayer bar, followed by drying at 130 C. for 2 minutes, thereby forming an anti-reflective coating layer. Next, the anti-reflective coating layer was subjected to aging in an oven at 60 C. for 24 hours, thereby manufacturing a final anti-reflective film.

EXAMPLE 2

(46) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 1.3 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

EXAMPLE 3

(47) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 2.7 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

EXAMPLE 4

(48) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 3.4 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

EXAMPLE 5

(49) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 5.4 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

EXAMPLE 6

(50) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 7.9 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

EXAMPLE 7

(51) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 13.3 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

EXAMPLE 8

(52) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 7.9 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used, and that NH.sub.4OH was not used in preparation of the coating composition.

EXAMPLE 9

(53) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 7.9 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used, and that 60 parts by weight of a 60 nm hollow silica particle-isopropanol dispersion sol (Thrulya 4110, JGC C&C Co., Ltd., 20% w/w) was used and NH.sub.4OH was not used in preparation of the coating composition.

COMPARATIVE EXAMPLE 1

(54) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that a binder was prepared by condensation polymerization of only tetraethoxysilane without use of (3,3,3-trifluoropropyl)triethoxysilane.

COMPARATIVE EXAMPLE 1

(55) An anti-reflective coating composition and an anti-reflective film were manufactured in the same manner as in Example 1 except that 29 parts by weight of (3,3,3-trifluoropropyl)triethoxysilane was used.

(56) Evaluation

(57) 1. Index of Refraction of Coating Layer

(58) Index of refraction of the coating layer on the manufactured anti-reflective film was measured at wavelengths of 532 nm, 632.8 nm and 830 nm using a prism coupler, followed by calculation of index of refraction at 550 nm using Cauchy dispersion equation. Results are shown in Table 1.

(59) TABLE-US-00001 TABLE 1 Index of refraction Example 1 1.23 Example 2 1.23 Example 3 1.23 Example 4 1.23 Example 5 1.23 Example 6 1.23 Example 7 1.24 Example 8 1.23 Example 9 1.23 Comparative Example 1 1.26 Comparative Example 2 1.24

(60) As shown in Table 1, it was confirmed that the coating layer could realize an index of refraction of 1.23 corresponding to a theoretically optimum value when the PET substrate was used.

(61) 2. Water Contact Angle

(62) Water contact angle was measured on each of the anti-reflective films of Examples and Comparative Examples using an OCA200 contact angle tester (Dataphysics Co., Ltd.). Results are shown in Table 2.

(63) TABLE-US-00002 TABLE 2 Contact angle () Example 1 44 Example 2 47 Example 3 52 Example 4 55 Example 5 58 Example 6 64 Example 7 75 Example 8 69 Example 9 43 Comparative Example 1 15 Comparative Example 2 95

(64) As shown in Table 2, it could be confirmed that the coating layers of Examples had a water contact angle of 40 to 80 and the contact angle of the coating layer increased with increasing amount of (3,3,3-trifluoropropyl)triethoxysilane in the binder. In addition, it was confirmed that the coating layer had an increased contact angle due to reduction in pH when NH.sub.4OH was not used. Thus, it was confirmed that the contact angle could be appropriately adjusted by adjusting the amount of the fluoroalkyl group-containing organosilane compound and the pH of the coating composition.

(65) 3. Transmittance and Minimum Reflectance

(66) Transmittance of each of the manufactured anti-reflective films was measured using a CM-5 spectrophotometer (Konica Minolta Co., Ltd.). In addition, a back surface of each of the anti-reflective films was subjected to blackening treatment, followed by measurement of luminous reflectance and minimum reflectance. Results are shown in Table 3.

(67) TABLE-US-00003 TABLE 3 Luminous Transmittance reflectance Minimum (D65) (%) (D65) (%) reflectance (%) Example 1 95.8 0.9 0.9 Example 2 95.5 1.2 1.1 Example 3 94.3 1.4 1.3 Example 4 94.9 1.7 1.6 Example 5 95.3 1.7 1.6 Example 6 95.2 1.5 1.4 Example 7 94.9 1.7 1.5 Example 8 95.6 1.2 1.1 Example 9 96.2 0.7 0.6 Comparative Example 1 95.5 1.2 1.1 Comparative Example 2 96.0 0.7 0.6

(68) As shown in Table 3, the anti-reflective films of Examples had a transmittance of 94% or more, a luminous reflectance of 0.6% to 1.8%, and a minimum reflectance of 0.6% to 1.6%. From the results, it was confirmed that the anti-reflective films of Examples exhibited excellent anti-reflection.

(69) Although the present invention has been described with reference to some embodiments, it should be understood that the embodiments are provided for illustrative purposes only, and that various modifications, changes, alterations, and equivalent embodiments can be made by those skilled in the art without departing from the spirit and scope of the invention. Therefore, the scope of the invention should be limited only by the accompanying claims and equivalents thereof.