Patent Application
20230305206
The present disclosure relates to a film used for a display device, a display device including the same and a polyimide-based film.
Polymer resins having excellent insolubility, chemical resistance, heat resistance, radiation resistance, and low-temperature characteristics are used as automobile materials, aviation materials, spacecraft materials, insulating coatings, insulating films, protective films, and the like.
Recently, the use of a polymer film formed of a polymer resin instead of glass as a cover window of a display device has been considered with the goal of reducing the thickness and weight and increasing the flexibility of the display device. In order for the polymer film to be used as the cover window of the display device, the polymer film needs to have excellent physical properties such as hardness, abrasion resistance, and flexibility. In order to impart desired physical properties to the display device, a coating layer is formed on a substrate.
However, optical interference occurs in the film including the coating layer formed on the substrate due to the difference in optical properties between the coating layer and the substrate. As a result, interference fringes like rainbow light are generated on the surface of the film, and thus there is a problem in that the visibility of the film is deteriorated.
Therefore, the present disclosure has been made in view of the above problems, and it is one object of the present disclosure to provide a film having a reflectance oscillation ratio (Or) of 1.0 or less.
It is another object of the present disclosure to provide a film having a reflectance graph slope (Gr) of 0.122 or less.
In accordance with the present disclosure, the above and other objects can be accomplished by the provision of a film including a substrate and a first coating layer disposed on the substrate, wherein the film has a reflectance oscillation ratio Or, calculated using the following Equation 1, of 1.0 or less, and a reflectance graph slope Gr calculated using the following Equation 2, of 0.122 or less, based on a reflectance graph obtained by measuring reflectance in a wavelength range of 380 nm to 780 nm:
O
r=[(Om1*Om2)−(Om1+Om2)]/Min(Om1,Om2) <Equation 1>
G
r=|(Rm1−Rm2)|/Rm2 <Equation 2>
wherein in Equation 1, Om1 is a mean Om of reflectance oscillation values in a wavelength range of 500 nm to 550 nm, and Om2 is a mean Om of reflectance oscillation values in a wavelength range of 650 nm to 780 nm,
wherein the means Om1 and Om2 of reflectance oscillation values are calculated using the following Equation 3, and Min(Om1, Om2) is a smaller mean Om of the means Om1 and Om2 of reflectance oscillation values,
wherein in Equation 2, Rm1 is an arithmetic mean of a reflectance corresponding to a first peak P1 and a reflectance corresponding to a first valley V1 in a wavelength range of 500 nm to 780 nm in the reflectance graph, and Rm2 is an arithmetic mean of a reflectance value corresponding to a final peak Pf and a reflectance value corresponding to a final valley Vf in the wavelength range of 500 nm to 780 nm in the reflectance graph,
O
m=(1/n)*Σ(Ok) <Equation 3>
wherein in Equation 3, Ok is an oscillation value in the corresponding wavelength range, and n is a number of oscillation values in the corresponding wavelength range, and
wherein each of the oscillation values is a difference in reflectance values corresponding to a pair of a peak Pk and a valley Vk adjacent to each other (|a reflectance corresponding to Pk−a reflectance corresponding to Vk|).
The substrate may be birefringent.
The substrate may have an X-axis direction refractive index Nx of 1.57 to 1.67, a Y-axis direction refractive index Ny of 1.57 to 1.67, and a Z-axis direction refractive index Nz of 1.53 to 1.57.
The first coating layer may have a refractive index N1 satisfying the following Equation 4:
0.927*Nx≤N1≤0.978*Ny <Equation 4>
The film may further include a second coating layer disposed on the substrate.
The second coating layer may be disposed between the substrate and the first coating layer.
The first coating layer may be disposed between the substrate and the second coating layer.
The second coating layer may have a refractive index N2 satisfying the following Equation 5:
0.793*Nx≤N2≤0.975*Ny <Equation 5>
The film may further include a third coating layer disposed on the substrate.
The third coating layer may have a refractive index (N3) satisfying the following Equation 6:
0.793*Nx≤N3≤0.975*Ny <Equation 6>
The first coating layer may include a light-transmissive matrix and particles dispersed in the light-transmissive matrix.
The light-transmissive matrix may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin.
The particles may include at least one of zirconia (ZrO2), silica (SiO2), alumina (Al2O3), titanium dioxide (TiO2), styrene, or acryl.
The first coating layer may have a thickness of 0.01 to 3.4 μm.
The second coating layer may have a thickness of 1 to 14 μm.
The third coating layer may have a thickness of 1 μm or less.
In accordance with another aspect of the present disclosure, there is provided a polyimide-based film including a polyimide-based substrate and a first coating layer disposed on the polyimide-based substrate, wherein the film has a reflectance oscillation ratio Or, calculated using the following Equation 1, of 1.0 or less, and a reflectance graph slope Gr, calculated using the following Equation 2, of 0.122 or less, based on a reflectance graph obtained by measuring reflectance in a wavelength range of 380 nm to 780 nm:
O
r=[(Om1*Om2)−(Om1+Om2)]/Min(Om1,Om2) <Equation 1>
G
r=|(Rm1−Rm2)|/Rm2 <Equation 2>
wherein in Equation 1, Om1 is a mean Om of reflectance oscillation values in a wavelength range of 500 nm to 550 nm, and Om2 is a mean Om of reflectance oscillation values in a wavelength range of 650 nm to 780 nm,
wherein the means Om1 and Om2 of reflectance oscillation values are calculated using the following Equation 3, and Min(Om1, Om2) is a smaller mean Om of the means Om1 and Om2 of reflectance oscillation values,
wherein in Equation 2, Rm1 is an arithmetic mean of a reflectance corresponding to a first peak P1 and a reflectance corresponding to a first valley V1 in a wavelength range of 500 nm to 780 nm in the reflectance graph, and Rm2 is an arithmetic mean of a reflectance value corresponding to a final peak Pf and a reflectance value corresponding to a final valley Vf in the wavelength range of 500 nm to 780 nm in the reflectance graph,
O
m=(1/n)*Σ(Ok) <Equation 3>
wherein in Equation 3, Ok is an oscillation value in the corresponding wavelength range, and n is a number of oscillation values in the corresponding wavelength range, and
wherein each of the oscillation values is a difference in reflectance values corresponding to a pair of a peak Pk and a valley Vk adjacent to each other (|a reflectance corresponding to Pk−a reflectance corresponding to Vk|).
In accordance with another aspect of the present disclosure, there is provided a display device including a display panel and the film disposed on the display panel.
In general, unlike glass, a polymer film includes a coating layer on a substrate so as to improve physical properties such as hardness, abrasion resistance and flexibility, but an interference fringe may occur in the film including the substrate and the coating layer due to differences in optical properties between the substrate and the coating layer.
According to an embodiment of the present disclosure, a film that prevents the formation of interference fringe and improves visibility can be manufactured by adjusting the reflectance oscillation ratio Or of the film to 1.0 or less and the reflectance graph slope Gr of the film to 0.122 or less.
In addition, the film according to the embodiment of the present disclosure has excellent optical and mechanical properties and thus effectively protects a display surface of a display device when used as a cover window of the display device.
The above and other objects, features and other advantages of the present disclosure will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
Hereinafter, preferred embodiments of the present disclosure will be described in more detail with reference to the attached drawings. These embodiments are provided for illustration so that this disclosure will be thorough and complete, and should not be construed as limiting the scope of the present disclosure.
The shapes, sizes, ratios, angles, numbers, etc. disclosed in the drawings for describing the embodiments of the present disclosure are exemplary, and thus the present disclosure is not limited to the items shown in the drawings. Like reference numbers refer to like elements throughout the description of the figures. Detailed descriptions of the related well-known art may be omitted when these may unnecessarily make the subject matter of the present disclosure unclear.
When the terms “include”, “have”, and “consist of”, etc. mentioned herein are used, another element may be added, unless the expression “only” is used. Singular forms are intended to include plural forms as well, unless the context clearly indicates otherwise. In addition, constituent elements are to be interpreted as including error ranges even if there is no explicit description thereof.
In the description of positional relationships, for example, when a positional relationship between two elements is described using “on”, “upper”, “lower”, and “next to”, at least one other element may be present between the two elements, unless the term “immediately” or “directly” is used.
Spatially relative terms such as “below”, “beneath”, “lower”, “above”, or “upper” may be used herein to describe a relationship of a device or an element to another device or another element as shown in the figures. It will be understood that spatially relative terms are intended to encompass different orientations of a device during the use or operation of the device, in addition to the orientation depicted in the figures. For example, if a device in one of the figures is turned upside down, elements described as “below” or “beneath” other elements would then be oriented “above” the other elements. The exemplary term “below” or “beneath” can, therefore, encompass both an orientation of below and above. In the same manner, the exemplary term “above” or “upper” can encompass both an orientation of above and below.
In describing a temporal relationship, for example, when the temporal order is described as “after”, “subsequent”, “next”, and “before”, the case which is not continuous may be included, unless “just” or “directly” is used.
It will be understood that, although the terms “first”, “second”, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are used only to distinguish one element from another. Therefore, a first element described below could be termed a second element within a technical idea of the present disclosure.
It should be understood that the term “at least one” includes all combinations related with any one item. For example, “at least one among a first element, a second element, and a third element” may include all combinations of two or more elements selected from among the first, second, and third elements as well as each element of the first, second, and third elements.
Features of various embodiments of the present disclosure may be partially or completely coupled to or combined with each other, and may be variously inter-operated with each other and driven technically as will be easily understood by those skilled in the art. The embodiments of the present disclosure may be carried out independently from each other, or may be carried out together in an interrelated manner.
As shown in
In one aspect, the film has a reflectance oscillation ratio Or, calculated using the following Equation 1, of 1.0 or less, and a reflectance graph slope Gr, calculated using the following Equation 2, of 0.122 or less, based on a reflectance graph obtained by measuring the reflectance in a wavelength region of 380 nm to 780 nm:
O
r=[(Om1*Om2)−(Om1+Om2)]/Min(Om1,Om2) <Equation 1>
G
r=|(Rm1−Rm2)|/Rm2 <Equation 2>
Hereinafter, the reflectance oscillation ratio Or of the film will be described with reference to
The reflectance oscillation ratio Or of the film may be calculated in accordance with Equation 1 above from the reflectance graph of the film of
In Equation 1, Om1 is the mean Om of reflectance oscillation values in a wavelength range of 500 nm to 550 nm, Om2 is the mean Om of reflectance oscillation values in a wavelength range of 650 nm to 780 nm, and Min (Om1, Om2) is a smaller mean Om of the means Om1 and Om2 of reflectance oscillation values.
The means of the reflectance oscillation values Om1 and Om2 are calculated using the following Equation 3:
O
m=(1/n)*Σ(Ok) <Equation 3>
wherein Ok is an oscillation value in the corresponding wavelength range and n is the number of oscillation values in the corresponding wavelength range.
Hereinafter, a method of calculating the means Om1 and Om2 of the reflectance oscillation values in accordance with Equation 3 will be described in more detail with reference to
In the graph of
As shown in
The reflectance oscillation ratio Or can be calculated using Equation 1 above using the mean Om1 of the reflectance oscillation values calculated using Equation 3 in the wavelength range of 500 nm to 550 nm W1, and the mean Om2 of the reflectance oscillation values calculated using Equation 3 in the wavelength range of 650 nm to 780 nm W2.
According to an embodiment of the present disclosure, the reflectance oscillation ratio Or is 1.0 or less.
The reflectance oscillation ratio Or of the present disclosure refers to the extent of change of the reflectance of the film caused by optical interference upon the change of the wavelength, and as the reflectance oscillation ratio Or increases, the optical interference increases, and as the reflectance oscillation ratio Or decreases, optical interference decreases.
When the reflectance oscillation ratio Or is 1.0 or less, the extent of change in reflectance according to the change in wavelength is reduced, the reflected light appears uniform to the human eye and an interference fringe is not observed thereby. On the other hand, when the reflectance oscillation ratio Or is higher than 1.0, the extent of change in reflectance according to the change in wavelength increases, the reflected light appears non-uniform to the human eye, and an interference fringe with various colors formed at narrow intervals can be produced on the surface of the film.
Hereinafter, the reflectance graph slope Gr will be described with reference to
The reflectance graph slope Gr of the film may be calculated in accordance with Equation 2 above from the reflectance graph of the film of
In Equation 2, Rm1 is the arithmetic mean of the reflectance value corresponding to a first peak P1 and the reflectance value corresponding to a first valley V1 in the reflectance graph in the wavelength range of 500 nm to 780 nm, and Rm2 is the arithmetic mean of the reflectance value corresponding to a final peak Pf and the reflectance value corresponding to a final valley Vf in the reflectance graph in the wavelength range of 500 nm to 780 nm.
As shown in
Therefore, in an embodiment of the present disclosure, the reflectance graph slope Gr that can be used to determine the slope behavior throughout the entire wavelength range of 500 nm to 780 nm can be calculated in accordance with Equation 2 above by obtaining the mean Rm1 of the reflectance corresponding to the first peak P1 and the reflectance corresponding to the first valley V1 in the wavelength region from the reflectance graph and the mean Rm2 of the reflectance corresponding to the final peak Pf and the reflectance corresponding to the final valley Vf.
According to an embodiment of the present disclosure, the reflectance graph slope Gr is 0.122 or less.
The reflectance graph slope Gr of the present disclosure means the extent of increase or decrease in the reflectance of the film according to wavelength, and when the reflectance rapidly increases or decreases according to a change in the wavelength, the reflectance graph slope Gr increases. As the reflectance graph slope Gr increases, the reflected light appears non-uniform to the human eye, so an interference fringe of various colors appears over a wide area. On the other hand, as the reflectance graph slope Gr decreases, the reflected light appears uniform to the human eye.
When the reflectance graph slope Gr is 0.122 or less, optical interference is reduced and no interference fringe is generated. On the other hand, when the reflectance graph slope Gr is higher than 0.122, optical interference may increase and an interference fringe may be produced on the surface of the film.
According to an embodiment of the present disclosure, the substrate 10 includes a transparent polymer. Any transparent polymer may be used as the substrate 10 according to an embodiment of the present disclosure, without any particular limitation. Examples of the polymer include homopolymers, such as polyimide-based polymer, polyester-based polymer, polyolefin-based polymer, norbornene-based polymer, polycarbonate-based polymer, polyethersulfone-based polymer, polyarylate-based polymer, polyacrylic-based polymer, polyethylene terephthalate-based polymer and cellulose-based polymers, copolymers thereof, epoxy-based polymers thereof, and the like.
In particular, the polyimide-based polymer has excellent physical properties, such as thermal properties, hardness, abrasion resistance, and flexibility, as well as optical properties, such as light transmittance and haze, and thus is preferably used as a substrate for a film used as a cover window of a display device, but the present disclosure is not limited thereto. In the present disclosure, the polyimide-based polymer refers to a polymer including a repeating unit having an imide functional group in a main chain structure, and is generally formed through condensation between an amine and carboxylic anhydride. In addition, the polyimide-based polymer may include an amide repeating unit. For example, the polyimide-based polymer according to an embodiment of the present disclosure is a polyamide-imide polymer.
The type of the film 100 may vary depending on the polymer of the substrate 10. For example, the film 100 including the substrate 10 containing a polyimide-based polymer may be referred to as a “polyimide-based film”.
According to an embodiment of the present disclosure, the polymer is optically anisotropic, and thus the substrate is birefringent.
The substrate 10 has an X-axis direction refractive index Nx of 1.57 to 1.67, a Y-axis direction refractive index Ny of 1.57 to 1.67, and a Z-axis direction refractive index Nz of 1.53 to 1.57.
In the present disclosure, the Z-axis direction of the substrate refers to a height direction of the substrate, and the X-axis direction and the Y-axis direction of the substrate are determined according to the refractive indices in the horizontal and vertical directions. In the present disclosure, among the refractive index in the horizontal direction and the refractive index in the vertical direction, the direction of the larger value of the refractive index is the X-axis direction, and the direction of the smaller value of the refractive index is the Y-axis direction.
Therefore, the refractive index in the X-axis direction Nx of the substrate refers to the larger refractive index among the refractive index in the horizontal direction and the refractive index in the vertical direction of the substrate, the refractive index in the Y-axis direction Ny of the substrate refers to the smaller refractive index among the refractive index in the horizontal direction and the refractive index in the vertical direction of the substrate, and the refractive index in the Z-axis direction of the substrate Nz refers to the refractive index in the height direction of the substrate.
When the refractive index in each direction of the substrate does not fall within the above range, an interference fringe may be generated due to the difference in refractive index between the substrate and the coating layer.
According to an embodiment of the present disclosure, the substrate 10 may have a thickness of 100 μm or less.
Hereinafter, the first coating layer 20 of the present disclosure will be described in detail with reference to
The first coating layer 20 is disposed on the substrate 10, and serves to control the reflectance oscillation ratio Or and the reflectance graph slope Gr of the film.
According to an embodiment of the present disclosure, the first coating layer 20 may include a light-transmissive matrix 21 and particles 22 dispersed in the light-transmissive matrix 21.
The first coating layer 20 including the light-transmissive matrix 21 and particles 22 dispersed in the light-transmissive matrix 21 is shown in
The particles 22 dispersed in the light-transmissive matrix of the first coating layer 20 control the reflectance oscillation ratio Or of the film and the reflectance graph slope Gr of the film, and thereby control the refractive index of the first coating layer 20.
According to an embodiment of the present disclosure, the light-transmissive matrix 21 of the first coating layer may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin.
In an embodiment of the present disclosure, the particles include at least one of zirconia (ZrO2), silica (SiO2), alumina (Al2O3), titanium dioxide (TiO2), styrene, or acryl. In particular, zirconia is advantageous in preventing the generation of an interference fringe by controlling the refractive index of the first coating layer and controlling the reflectance oscillation ratio Or of the film and the reflectance graph slope Gr of the film.
The first coating layer 20 may be formed using a first coating composition. The first coating composition may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin. The first coating composition may include particles. The first coating composition may include a solvent.
In order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less, the type of the light-transmissive matrix 21 of the first coating layer 20, the type of particles 22 included in the first coating layer 20, the content of particles 22 included in the first coating layer 20, the refractive index of the first coating layer 20, the thickness of the first coating layer 20, and the “solvent of the first coating composition” for the formation of the first coating layer 20 may be controlled.
According to an embodiment of the present disclosure, the type of the light-transmissive matrix 21 of the first coating layer 20 may be controlled in order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less.
The light-transmissive matrix 21 of the first coating layer 20 may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin.
Depending on the type of the light-transmissive matrix 21 of the first coating layer 20, the refractive index of the first coating layer 20 may vary, and the reflectance oscillation ratio Or and the reflectance graph slope Gr may be controlled.
According to an embodiment of the present disclosure, the particles 22 included in the first coating layer 20 may be controlled in order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less.
The particles 22 may include at least one of zirconia, silica, alumina, titanium dioxide, styrene, or acryl. Preferably, the particles 22 may include zirconia.
The particles 22 in the first coating layer 20 can control the refractive index of the first coating layer 20, thereby adjusting the reflectance oscillation ratio Or of the film to 1.0 or less, and the reflectance graph slope Gr of the film to 0.122 or less. In particular, the use of zirconia makes it easy to control the refractive index of the first coating layer 20.
According to an embodiment of the present disclosure, the content of the particles 22 included in the first coating layer 20 may be controlled in order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less.
According to an embodiment of the present disclosure, the particles 22 are present in the first coating layer 20 in an amount of 10 to 50 parts by weight, based on 100 parts by weight of the light-transmissive matrix 21.
When the particles 22 are present in the first coating layer 20 in an amount of less than 10 parts by weight or more than 50 parts by weight based on 100 parts by weight of the light-transmissive matrix 21, the reflectance oscillation ratio Or of the film is higher than 1, or the reflectance graph slope Gr of the film is higher than 0.122.
According to an embodiment of the present disclosure, the first coating layer 20 may have a refractive index N1 determined using Equation 4 below in consideration of the X-axis and Y-axis refractive indices of the substrate.
0.927*Nx≤N1≤0.978*Ny <Equation 4>
When the refractive index N1 of the first coating layer does not fall within the above range, the reflectance oscillation ratio Or of the film 100 is higher than 1, or the reflectance graph slope Gr of the film 100 is higher than 0.122.
Therefore, in order to adjust the reflectance oscillation ratio Or of the film 100 to 1.0 or less and the reflectance graph slope Gr to 0.122 or less, the refractive index of the first coating layer 20 can be controlled within the range of Equation 4 above.
According to an embodiment of the present disclosure, the first coating layer 20 may have a thickness of 0.01 to 3.4 μm, preferably a thickness of 0.07 to 1.3 μm in order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less.
By controlling the thickness of the first coating layer within the range of 0.01 to 3.4 μm, a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less can be produced.
When the thickness of the first coating layer 20 is less than 0.01 μm, coating stability and the thickness of the swelling layer 12 are reduced, so the effect of controlling the reflectance oscillation ratio Or is insufficient. In addition, when the thickness of the first coating layer 20 is higher than 3.4 μm, the reflectance oscillation ratio Or is higher than 1.0.
According to an embodiment of the present disclosure, by controlling the solvent of the first coating composition for forming the first coating layer 20, a film having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less can be produced.
Specifically, the solvent of the first coating composition may include at least one of methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), propylene glycol methyl ether (PGME), or ethyl acetate (EA). In particular, the solvent preferably includes MEK.
According to an embodiment of the present disclosure, the solvent of the first coating composition may include MEK, along with at least one of MIBK, PGME, or EA.
According to an embodiment of the present disclosure, a mass ratio of MEK to at least one of MIBK, PGME, or EA in the solvent of the first coating composition may be 8:2 to 6:4.
A swelling layer may be formed by the solvent of the first coating composition.
According to another embodiment of the present disclosure, the film 101 may further include the swelling layer 12.
The swelling layer 12 may be disposed between the residual substrate layer 11 and the first coating layer 20.
Hereinafter, the swelling layer 12 will be described with reference to
The swelling layer 12 may be formed by the solvent of the first coating composition.
As shown in
According to an embodiment of the present disclosure, the substrate 10 may include the residual substrate layer 11 and the swelling layer 12.
By disposing the swelling layer 12 between the residual substrate layer 11 and the first coating layer 20, the reflectance oscillation ratio Or of the film 101 may be set to 1.0 or less, and the reflectance graph slope Gr thereof may be set to 0.122 or less.
The swelling layer 12 may have a refractive index of 1.66 or less.
In order to adjust the reflectance oscillation ratio Or and the reflectance graph slope Gr of the film 101 to 1.0 or less and 0.122 or less, respectively, the refractive index of the swelling layer 12 may be controlled to 1.66 or less.
When the refractive index of the swelling layer 12 is greater than 1.66, disadvantageously, the reflectance oscillation ratio Or is greater than 1.0, and an interference fringe is observed on the surface of the film 101.
The swelling layer 12 may have a thickness of 10 to 50% of the thickness of the first coating layer 20.
In order to adjust the reflectance oscillation ratio Or and the reflectance graph slope Gr of the film 101 to 1.0 or less and 0.122 or less, respectively, the thickness of the swelling layer 12 can be controlled within the range of to 50% of the thickness of the first coating layer 20.
When the thickness of the swelling layer 12 is less than 10% of the thickness of the first coating layer 20, the adhesion between the substrate 10 and the first coating layer may be deteriorated. On the other hand, when the thickness of the swelling layer 12 is higher than 50%, the flexibility of the film 101 may be reduced.
The thickness of the swelling layer 12 may vary depending on the type, content, and content ratio of the “solvent of the first coating composition”, as well as the drying time and temperature of the first coating layer 20.
In order to adjust the thickness of the swelling layer 12 to 10 to 50% of the thickness of the first coating layer 20, the solvent of the first coating composition includes MEK, along with at least one of MIBK, PGME, or EA.
In order to adjust the thickness of the swelling layer 12 to 10 to 50% of the thickness of the first coating layer 20, the MEK and at least one of MIBK, PGME, or EA of the solvent of the first coating composition may be mixed at a weight ratio of 8:2 to 6:4.
In order to adjust the thickness of the swelling layer 12 to 10 to 50% of the thickness of the first coating layer 20, the thickness of the first coating layer 20 may be adjusted to 0.01 to 3.4 μm.
When the thickness of the first coating layer 20 is less than 0.01 μm, the coating stability is deteriorated and the thickness of the swelling layer 12 is reduced, so the effect of controlling the reflectance oscillation ratio Or is insufficient. In addition, when the thickness of the first coating layer 20 is higher than 3.4 μm, the reflectance oscillation ratio Or is higher than 1.0, an interference fringe is generated, and the visibility of the film may be deteriorated.
In order to adjust the thickness of the swelling layer 12 to 10 to 50% of the thickness of the first coating layer 20, gradation drying may be performed in a stepwise manner including drying at 50 to 60° C. for 1 to 2 minutes, at 70 to 80° C. for 2 to 3 minutes, and at 90 to 100° C. for 2 to 3 minutes in the process of preparing the first coating layer 20.
When the temperature in each step is higher than the upper limit in the process of producing the first coating layer 20, problems in which the solvent is rapidly volatilized and the swelling layer 12 is not sufficiently formed may occur, and when the temperature in each step is less than the lower limit, a problem in which the thickness of the swelling layer 12 is greater than the range defined in the present disclosure may occur.
When the drying time of the first coating layer 20 is longer than the upper limit in each step, a problem in which the thickness of the swelling layer 12 is greater than the range defined in the present disclosure may occur, and when the time is shorter than the lower limit in each step, a problem in which the swelling layer 12 is not sufficiently formed may occur.
The production method may be controlled in order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less. For example, in order to produce a film 100 having a reflectance oscillation ratio Or of 1.0 or less and a reflectance graph slope Gr of 0.122 or less, a drying method may be controlled during the process of producing the first coating layer 20.
For example, when preparing the first coating layer 20, gradation drying may be performed in a stepwise manner at 50 to 60° C. for 1 to 2 minutes, at 70 to 80° C. for 2 to 3 minutes, and then at 90 to 100° C. for 2 to 3 minutes.
As such, by adjusting the components, refractive index, thickness, and production method of the first coating layer 20, the reflectance oscillation ratio Or and the reflectance graph slope Gr of the film can be controlled and the refractive index of the first coating layer can be controlled.
According to another embodiment of the present disclosure, the film 102 may further include a second coating layer 30 on the substrate 10.
As shown in
As shown in
The reflectance oscillation ratio Or and the reflectance graph slope Gr of the film 102 may also be controlled using the second coating layer 30.
The second coating layer 30 is a layer that protects the substrate 10 or the first coating layer 20 and the adhered to which the film 102 is attached from the external environment, and the second coating layer 30 may be a hard coating layer.
According to an embodiment of the present disclosure, the second coating layer 30 may have a refractive index N2 determined according to Equation 5 below, based on the X-axis and Y-axis refractive indices of the substrate.
0.793*Nx≤N2≤0.975*Ny <Equation 5>
When the refractive index N2 of the second coating layer does not fall within the above range, the reflectance oscillation ratio Or of the film is higher than 1, or the reflectance graph slope Gr of the film is higher than 0.122.
According to another embodiment of the present disclosure, the second coating layer 30 may include a light-transmissive matrix.
The light-transmissive matrix of the second coating layer 30 may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin. The light-transmissive matrix of the second coating layer 30 may be the same as or different from the light-transmissive matrix of the first coating layer 20, but the present disclosure is not limited thereto. However, it is preferable that the same light-transmissive matrix is used because adhesion between the first and second coating layers increases.
According to another embodiment of the present disclosure, the second coating layer 30 may have a thickness of 1 to 14 μm, preferably a thickness of 3 to 7 μm, but the present disclosure is not limited thereto.
By controlling the thickness of the second coating layer 30, the reflectance oscillation ratio Or of the film 102 and the reflectance graph slope Gr of the film can be controlled and the refractive index of the second coating layer 30 can be controlled.
The second coating layer 30 may be formed using the second coating composition. The second coating composition may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin. The second coating composition may include a solvent.
According to another embodiment of the present disclosure, a film 103 may further include a third coating layer 40 on the substrate 10.
According to another embodiment of the present disclosure, the third coating layer 40 may have a refractive index N3 satisfying the following Equation 6 based on the X-axis and Y-axis refractive indices of the substrate.
0.793*Nx≤N3≤0.975*Ny <Equation 6>
When the refractive index N3 of the third coating layer does not fall within the above range, the reflectance oscillation ratio Or of the film is higher than 1, or the reflectance graph slope Gr of the film is higher than 0.122.
According to another embodiment of the present disclosure, the third coating layer 40 may include a light-transmissive matrix.
The light-transmissive matrix of the third coating layer 40 may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin. The light-transmissive matrix of the third coating layer 40 may be the same as or different from the light-transmissive matrix of the first coating layer 20 or the second coating layer 30, but the present disclosure is not limited thereto.
According to another embodiment of the present disclosure, the third coating layer 40 may have a thickness of 1 μm or less, preferably a thickness of 0.1 μm or less, but the present disclosure is not limited thereto.
By controlling the thickness of the third coating layer 40, the reflectance oscillation ratio Or of the film 102 and the reflectance graph slope Gr of the film can be controlled, and the refractive index of the second coating layer 30 can be controlled.
The third coating layer 40 may be formed using the third coating composition. The third coating composition may include at least one of a siloxane-based resin, an acrylic-based resin, a urethane-based resin, or an epoxy-based resin. The third coating composition may include a solvent.
In another aspect, the present disclosure is directed to a display device including a display panel and the film disposed on the display panel. The film of the display device may include the film according to one embodiment of the present disclosure.
The display panel includes a substrate, a thin film transistor (TFT) on the substrate, and an organic light-emitting device connected to the thin film transistor (TFT). The organic light-emitting device includes a first electrode, an organic light-emitting layer on the first electrode, and a second electrode on the organic light-emitting layer. The display device may be an organic light-emitting display device.
The substrate may be made of glass or plastic. Specifically, the substrate may be made of a plastic such as a polyimide-based resin or a polyimide-based film. A buffer layer may be disposed on the substrate.
A thin film transistor (TFT) is disposed on the substrate. The thin film transistor (TFT) includes a semiconductor layer, a gate electrode insulated from the semiconductor layer and overlapping at least a portion of the semiconductor layer, a source electrode connected to the semiconductor layer, and a drain electrode spaced apart from the source electrode and connected to the semiconductor layer.
A gate insulating film is disposed between the gate electrode and the semiconductor layer. An interlayer insulating layer may be disposed on the gate electrode, and the source electrode and the drain electrode may be disposed on the interlayer insulating layer.
A planarization layer is disposed on the thin film transistor TFT to planarize the top of the thin film transistor TFT.
The first electrode is disposed on the planarization layer. The first electrode is connected to the thin film transistor TFT through a contact hole provided in the planarization layer.
The bank layer is disposed in a portion of the first electrode on the planarization layer to define a pixel area or a light-emitting area. For example, the bank layer is disposed in the form of a matrix in the corresponding boundaries between a plurality of pixels to define the respective pixel regions.
The organic light-emitting layer is disposed on the first electrode. The organic light-emitting layer may also be disposed on the bank layer. The organic light-emitting layer may include one light-emitting layer or two light-emitting layers stacked in a vertical direction. Light having any one color of red, green, and blue may be emitted from the organic light-emitting layer, and white light may be emitted therefrom.
The second electrode is disposed on the organic light-emitting layer.
The first electrode, the organic light-emitting layer, and the second electrode may be stacked to constitute the organic light-emitting device.
When the organic light-emitting layer emits white light, each pixel may include a color filter for filtering the white light emitted from the organic light-emitting layer based on respective wavelengths. The color filter is formed on the passage of light.
A thin film encapsulation layer may be disposed on the second electrode. The thin film encapsulation layer may include at least one organic layer and at least one inorganic layer, and the at least one organic layer and the at least one inorganic layer may be alternately disposed.
The film according to an embodiment of the present disclosure is disposed on the display panel having the stack structure described above.
Hereinafter, the present disclosure will be described in more detail with reference to Preparation Examples and Examples. The Preparation Examples and Examples are provided only for better understanding of the present disclosure, and should not be construed as limiting the scope of the present disclosure.
735.264 g of N,N-dimethylacetamide (DMAc) was charged in a 1 L reactor equipped with a stirrer, a nitrogen injector, a dropping funnel, a temperature controller, and a cooler, while nitrogen was passed through the reactor, the temperature of the reactor was adjusted to 25° C., 54.439 g (0.17 mol) of 2,2′-bis(trifluoromethyl)benzidine (TFDB) was dissolved therein, and the resulting solution was maintained at 25° C. 10.003 g (0.034 mol) of biphenyl-tetracarboxylic acid dianhydride (BPDA) was added thereto, followed by stirring for 3 hours to thoroughly dissolve the BPDA, and then 15.105 g (0.034 mol) of 4,4′-(hexafluoroisopropylidene) diphthalic anhydride (6FDA) was added thereto and completely dissolved therein. The reactor temperature was dropped to 10° C., 20.716 g (0.102 mol) of terephthaloyl chloride (TPC) was added thereto, and the reaction was allowed to proceed at 25° C. for 12 hours to obtain a polymer solution having a solid content of 12% by weight.
11.833 g of pyridine and 15.110 g of acetic anhydride were added to the obtained polymer solution, followed by stirring for 30 minutes and then further stirring at 70° C. for 1 hour. The resulting product was allowed to cool to room temperature, 20 L of methanol was added to the resulting polymer solution to precipitate a solid powder, and the precipitated solid powder was filtered, pulverized, washed again with 2 L of methanol, and then dried at 100° C. in a vacuum for 6 hours to obtain a powdery polyimide-based polymer solid. The polyimide-based polymer solid powder prepared herein was a polyamide-imide polymer solid powder.
550 g of DMAc was charged in a 1 L reactor and then stirred for a predetermined period of time while the temperature of the reactor was maintained at 10° C. Then, 75 g of the prepared polyimide-based polymer solid powder was added thereto, the resulting mixture was stirred for 1 hour, and the temperature was raised to 25° C. to prepare a liquid polyimide-based resin solution.
The obtained polyimide-based resin solution was applied to a glass substrate using an applicator and dried with hot air at 130° C. for 30 minutes to prepare a film, and then the prepared film was peeled off the glass substrate and fixed to a frame using a pin.
The frame to which the film was fixed was placed in a vacuum oven and slowly heated from 100° C. to 300° C. over 2 hours, then slowly cooled and separated from the frame to obtain a high-refractive-index polyimide-based substrate. The high-refractive-index polyimide-based substrate was heat-treated at 250° C. for 5 minutes.
The high-refractive-index polyimide-based substrate has a thickness of 50 μm, is light-transmissive, and is birefringent. The substrate has refractive indices of Nx=Ny=1.65 and Nz=1.55.
734.06 g of N,N-dimethylacetamide (DMAc) was charged in a 1 L reactor equipped with a stirrer, a nitrogen injector, a dropping funnel, a temperature controller and a cooler, while nitrogen was passed through the reactor, the temperature of the reactor was adjusted to 25° C., 44.832 g (0.14 mol) of TFDB was dissolved therein, and the resulting solution was maintained at 25° C. 8.238 g (0.028 mol) of BPDA was added thereto, followed by stirring for 3 hours to thoroughly dissolve the BPDA, and then 49.756 g (0.112 mol) of 6FDA was added thereto and the reaction was allowed to proceed at 25° C. for 12 hours to obtain a polymer solution having a solid content of 12% by weight.
24.36 g of pyridine and 31.11 g of acetic anhydride were added to the obtained polymer solution, followed by stirring for 30 minutes and then further stirring at 70° C. for 1 hour. The result was allowed to cool to room temperature, 20 L of methanol was added to the resulting polymer solution to precipitate a solid powder, and the precipitated solid powder was filtered, pulverized, washed again with 2 L of methanol, and then dried at 100° C. in a vacuum for 6 hours to obtain a powdery polyimide-based polymer solid. The polyimide-based polymer solid powder prepared herein was a polyamide-imide polymer solid powder.
Then, a low-refractive-index polyimide-based substrate was prepared in the same manner as in Preparation Example 1 using the prepared polyimide-based polymer solid powder.
The low-refractive-index polyimide-based substrate has a thickness of 50 μm, is light-transmissive, and is birefringent. The substrate has refractive indices of Nx=Ny=1.57 and Nz=1.53.
776.655 g of N,N-dimethylacetamide (DMAc) was charged in a 1 L reactor equipped with a stirrer, a nitrogen injector, a dropping funnel, a temperature controller and a cooler, while nitrogen was passed through the reactor, the temperature of the reactor was adjusted to 25° C., 54.439 g (0.17 mol) of TFDB was dissolved therein, and the resulting solution was maintained at 25° C. 15.005 g (0.051 mol) of BPDA was added thereto, followed by stirring for 3 hours to thoroughly dissolve the BPDA, and then 22.657 g (0.051 mol) of 6FDA was added thereto and completely dissolved therein, the reactor temperature was dropped to 10° C., 13.805 g (0.068 mol) of TPC was added thereto, and the reaction was allowed to proceed at 25° C. for 12 hours to obtain a polymer solution having a solid content of 12% by weight.
17.75 g of pyridine and 22.92 g of acetic anhydride were added to the obtained polymer solution, followed by stirring for 30 minutes and then further stirring at 70° C. for 1 hour. The result was allowed to cool to room temperature, 20 L of methanol was added to the resulting polymer solution to precipitate a solid powder, and the precipitated solid powder was filtered, pulverized, washed again with 2 L of methanol, and then dried at 100° C. in a vacuum for 6 hours to obtain a powdery polyimide-based polymer solid. The polyimide-based polymer solid powder prepared herein is a polyamide-imide polymer solid powder.
Then, a medium-refractive-index polyimide-based substrate was prepared in the same manner as in Preparation Example 1 using the prepared polyimide-based polymer solid powder.
The medium-refractive-index polyimide-based substrate has a thickness of 50 μm, is light-transmissive, and is birefringent. The substrate has refractive indices of Nx=Ny=1.62 and Nz=1.54.
2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (TCI CO., LTD.), TEOS (tetraethyl orthosilicate, Sigma-Aldrich, Inc.), and H2O were mixed at a ratio of 747.66 mL:38.28 mL:93.88 mL, the resulting mixture was added to a 1,500 mL flask, and then 0.1 g of sodium hydroxide was added thereto as a catalyst, followed by stirring at 60° C. for 10 hours. Then, the resulting product was filtered using a 0.45 um Teflon filter to obtain an epoxy-based resin.
Then, 600 mL of a dilution of MEK (methyl ethyl ketone) and MIBK (methyl isobutyl ketone) at a ratio of 8:2 was added to the prepared epoxy-based resin, IRGACURE 250 (BASF Corporation) as a photoinitiator was added to the prepared epoxy-based resin in an amount of 3 parts by weight with respect to the weight of the epoxy-based resin, and KT-300Z-S-KR (solid content of 42 wt %, cyclohexanone+MIBK+aliphatic solvent, Toyochem Co., Ltd.), as a zirconia dispersion, was added thereto in an amount of 30 parts by weight with respect to the epoxy-based resin on a solid basis to obtain a first coating composition having a refractive index of 1.57 when cured.
The high-refractive-index polyimide-based substrate produced in Preparation Example 1 was used as the substrate 10.
The first coating composition was applied to the upper surface of the high-refractive-index polyimide-based substrate of Preparation Example 1 using a bar, and then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 25 nm on the substrate.
Then, light having a wavelength of 315 nm was radiated at a dose of 1 J/cm2 from an ultraviolet lamp to produce a primary film including a first coating layer having a thickness of 100 nm.
Then, a second coating composition having a refractive index of 1.50 upon curing was prepared by excluding KT-300Z-S-KR (Toyochem Co., Ltd.), which is a zirconia dispersion, from the first coating composition. The second coating composition was applied to the upper surface of the cured film of the primary film using a bar and dried at 100° C. for 10 minutes, and light having a wavelength of 315 nm was radiated thereto at 2 J/cm2 from an ultraviolet lamp to produce a transparent polyimide-based film including a second coating layer having a thickness of 5 μm.
A first coating composition was prepared in the same manner as in Example 1, except that the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was added in an amount of 43 parts by weight with respect to the prepared epoxy-based resin on a solid basis. The refractive index upon curing of the first coating composition was 1.60.
A second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the high-refractive-index polyimide-based substrate produced in Preparation Example 1 in the same manner as in Example 1 using the prepared first and second coating compositions.
A first coating composition was prepared in the same manner as in Example 1, except that the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was added in an amount of 17 parts by weight with respect to the prepared epoxy-based resin on a solid basis. The refractive index upon curing of the first coating composition was 1.54.
A second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the high-refractive-index polyimide-based substrate produced in Preparation Example 1 in the same manner as in Example 1 using the prepared first and second coating compositions.
A first coating composition was prepared in the same manner as in Example 1, except that the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was added in an amount of 13 parts by weight with respect to the prepared epoxy-based resin on a solid basis. The refractive index upon curing of the first coating composition was 1.53.
A second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the low-refractive-index polyimide-based substrate produced in Preparation Example 2 in the same manner as in Example 1 using the prepared first and second coating compositions.
A first coating composition was prepared in the same manner as in Example 1, except that the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was added in an amount of 22 parts by weight with respect to the prepared epoxy-based resin on a solid basis. The refractive index upon curing of the first coating composition was 1.55.
A second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the medium-refractive-index polyimide-based substrate produced in Preparation Example 3 in the same manner as in Example 1 using the prepared first and second coating compositions.
A secondary film having the first and second coating layers was produced in the same manner as in Example 1.
Then, the second coating composition was applied to the other surface of the secondary film using a bar and then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 0.2 μm on the substrate. Then, light having a wavelength of 315 nm was radiated thereto at a dose of 2 J/cm2 using an ultraviolet lamp to produce a transparent polyimide-based film including a third coating layer having a thickness of 0.8 μm.
3-(trimethoxysilyl)propyl methacrylate (Sigma-Aldrich, Inc.), TEOS (Sigma-Aldrich, Inc.), and H2O were mixed at a ratio of 747.66 mL:38.28 mL:93.88 mL, the resulting mixture was added to a 1,500 mL flask, and then 0.1 g of sodium hydroxide was added thereto as a catalyst, followed by stirring at 60° C. for 10 hours. Then, the resulting product was filtered using a 0.45 um Teflon filter to obtain an acrylic-based resin.
Then, 600 mL of a dilution of MEK (methyl ethyl ketone) and MIBK (methyl isobutyl ketone) at a ratio of 8:2 was added to the prepared acrylic-based resin, IRGACURE 250 (BASF Corporation) as a photoinitiator was added to the prepared acrylic-based resin in an amount of 3 parts by weight with respect to the acrylic-based resin, and KT-300Z—S-KR (solid content of 42 wt %, cyclohexanone+MIBK+aliphatic solvent, Toyochem Co., Ltd.), as a zirconia dispersion, was added thereto in an amount of 30 parts by weight with respect to the acrylic-based resin on a solid basis to obtain a first coating composition having a refractive index of 1.57 when cured.
The high-refractive-index polyimide-based substrate produced in Preparation Example 1 was used as the substrate 10.
The first coating composition was applied to the upper surface of the high-refractive-index polyimide-based substrate of Preparation Example 1 using a bar and then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 25 nm on the substrate.
Then, light having a wavelength of 315 nm was radiated at a dose of 1 J/cm2 using an ultraviolet lamp to produce a primary film including a first coating layer having a thickness of 100 nm.
Then, a second coating composition having a refractive index of 1.50 upon curing was prepared by excluding KT-300Z—S-KR (Toyochem Co., Ltd.), which is a zirconia dispersion, from the first coating composition. The second coating composition was applied to the upper surface of the cured film of the primary film using a bar and dried at 100° C. for 10 minutes, and light having a wavelength of 315 nm was radiated at 2 J/cm2 from an ultraviolet lamp to produce a transparent polyimide-based film having a second coating layer having a thickness of 5 μm.
2-(3,4-epoxycylohexyl)ethyltrimethoxysilane (TCI CO., LTD.), TEOS (tetraethyl orthosilicate, Sigma-Aldrich, Inc.), and H2O were mixed at a ratio of 747.66 mL:38.28 mL:93.88 mL, the resulting mixture was added to a 1,500 mL flask, and then 0.1 g of sodium hydroxide was added thereto as a catalyst, followed by stirring at 60° C. for 10 hours. Then, the resulting product was filtered using a 0.45 um Teflon filter to obtain an epoxy-based resin.
Then, 600 mL of a dilution of MEK (methyl ethyl ketone) and MIBK (methyl isobutyl ketone) at a ratio of 8:2 was added to the prepared epoxy-based resin, and IRGACURE 250 (BASF Corporation) as a photoinitiator was added to the prepared epoxy-based resin in an amount of 3 parts by weight with respect to the epoxy-based resin to obtain an epoxy-based resin composition having a refractive index of 1.50 when cured.
The high-refractive-index polyimide-based substrate produced in Preparation Example 1 was used as the substrate 10.
The epoxy-based resin composition was applied to the upper surface of the high-refractive-index polyimide-based substrate of Preparation Example 1 using a bar and then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 25 nm on the substrate.
Then, light having a wavelength of 315 nm was radiated at a dose of 2 J/cm2 from an ultraviolet lamp to produce a transparent polyimide-based film including a single coating layer having a thickness of 5 μm.
A first coating composition was prepared in the same manner as in Example 1, except that the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was added in an amount of 60 parts by weight with respect to the prepared epoxy-based resin on a solid basis. The refractive index upon curing of the first coating composition was 1.64.
A second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the high-refractive-index polyimide-based substrate produced in Preparation Example 1 in the same manner as in Example 1 using the prepared first and second coating compositions.
A first coating composition was prepared in the same manner as in Example 1, except that the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was added in an amount of parts by weight with respect to the prepared epoxy-based resin on a solid basis. The refractive index upon curing of the first coating composition was 1.51.
A second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the high-refractive-index polyimide-based substrate produced in Preparation Example 1 in the same manner as in Example 1 using the prepared first and second coating compositions.
A first coating composition was prepared in the same manner as in Example 1. The refractive index upon curing of the first coating composition was 1.57.
The zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was further added to the first coating composition in an amount of 26 parts by weight (56 parts by weight in total) to prepare a second coating composition having a refractive index upon curing of 1.63.
A transparent polyimide-based film including first and second coating layers was produced on the upper surface of the high-refractive-index polyimide-based substrate produced in Preparation Example 1 in the same manner as in Example 1 using the prepared first and second coating compositions.
A first coating composition was prepared in the same manner as in Example 1. The refractive index upon curing of the first coating composition was 1.57.
The first coating composition was applied to the upper surface of the high-refractive-index polyimide-based substrate of Preparation Example 1 using a bar, and was then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 1.25 nm on the substrate.
Then, light having a wavelength of 315 nm was radiated at a dose of 1 J/cm2 from an ultraviolet lamp to produce a primary film including a first coating layer having a thickness of 100 nm.
Then, a second coating composition was prepared in the same manner as in Example 1.
A transparent polyimide-based film including first and second coating layers was produced by forming the second coating layer on the upper surface of the cured primary film in the same manner as in Example 1 using the prepared second coating composition.
A secondary film including the first and second coating layers was produced in the same manner as in Example 1.
Then, the zirconia dispersion KT-300Z-S-KR (Toyochem Co., Ltd.) was further added to the first coating composition in an amount of 26 parts by weight (56 parts by weight in total) to prepare a second coating composition having a refractive index upon curing of 1.63.
Then, the third coating composition was applied to the other surface of the secondary film using a bar and then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 0.2 μm on the substrate. Then, light having a wavelength of 315 nm was radiated at a dose of 2 J/cm2 from an ultraviolet lamp to produce a transparent polyimide-based film including a third coating layer having a thickness of 0.8 μm.
A secondary film including the first and second coating layers was produced in the same manner as in Example 1.
Then, the second coating composition was applied to the other surface of the secondary film using a bar and then dried at 60° C. for 2 minutes, 80° C. for 3 minutes, and 100° C. for 3 minutes to form a swelling layer resulting from the solvent to a mean thickness of 1.25 μm on the substrate. Then, light having a wavelength of 315 nm was radiated at a dose of 2 J/cm2 from an ultraviolet lamp to produce a transparent polyimide-based film including a third coating layer having a thickness of 5 μm.
The following characteristics of the films produced in Examples 1 to 7 and Comparative Examples 1 to 7 were measured.
(1) Adhesion
The degree of peeling after cutting into a grid pattern according to ASTM D3359 using a CC1000 model from TQC Ltd. was measured.
(2) Transmittance and Haze
Each of the final films produced according to Examples and Comparative Examples was cut to a size of 50 mm×50 mm, the transmittance and haze thereof were measured 5 times according to ASTM D1003 using an HM-150 haze meter from Murakami Color Research Lab., and the average thereof was determined.
(3) Reflectance Oscillation Ratio (Or) and Reflectance Graph Slope (Gr)
Light reflectance was measured in a wavelength range of 380 to 780 nm using the UH4150 apparatus from Hitachi Ltd. The reflectance oscillation ratio Or calculated using the following Equation 1 and the reflectance graph slope Gr calculated using the following Equation 2 were calculated from the measured reflectance graph of the film.
O
r=[(Om1*Om2)−(Om1+Om2)]/Min(Om1,Om2) <Equation 1>
G
r=|(Rm1−Rm2)|/Rm2 <Equation 2>
Wherein, in Equation 1, Om1 is the mean (Om) of reflectance oscillation values in a wavelength range of 500 nm to 550 nm, and Om2 is the mean (Om) of reflectance oscillation values in a wavelength range of 650 nm to 780 nm,
wherein the means Om1 and Om2 of the reflectance oscillation values are calculated using the following Equation 3, and Min(Om1, Om2) is a smaller mean of the means Om1 and Om2 of reflectance oscillation values, and in Equation 2, Rm1 is the arithmetic mean of the reflectance value corresponding to a first peak P1 and the reflectance value corresponding to a first valley V1 in the reflectance graph in the wavelength range of 500 nm to 780 nm, and Rm2 is the arithmetic mean of the reflectance value corresponding to a final peak Pf and the reflectance value corresponding to a final valley Vf in the wavelength range of 500 nm to 780 nm in the reflectance graph.
O
m=(1/n)*Σ(Ok) <Equation 3>
In Equation 3, Ok is an oscillation value in the corresponding wavelength range, and n is the number of oscillation values in the corresponding wavelength range,
wherein each of the oscillation values is the difference in reflectance values corresponding to a pair of a peak Pk and a valley Vk adjacent to each other (|the reflectance corresponding to Pk−the reflectance corresponding to Vk|).
(4) Interference Fringe
The films of Examples and Comparative Examples were visually evaluated under a three-wavelength lamp and evaluated based on the following grades.
The measurement results are shown in Table 1 below.
As can be seen from the measurement results shown in Table 1, the film according to the embodiment of the present disclosure exhibited excellent optical properties such as transmittance and haze as well as adhesion and flexibility between the substrate and the coating layer.
As can be seen from Example 1 and Comparative Example 1, the film provided with the reflectance oscillation ratio Or and the reflectance graph slope Gr within the range defined in the present disclosure by applying the first coating layer between the second coating layer and the substrate exhibited a better interference fringe than that of the film to which no coating layer was applied.
Comparing Examples 1 to 3 with Comparative Examples 2 to 3, even in the structure in which the first coating layer is applied between the second coating layer and the substrate, it can be seen that the effect of alleviating the interference fringe is not obtained when the refractive index does not fall within the range defined in the present disclosure, in other words, when the reflectance oscillation ratio Or is higher than 1.0.
In addition, as can be seen from Example 1 and Comparative Example 5, although the first coating layer is applied between the second coating layer and the substrate, when the thickness of the first coating layer deviates from the predetermined range and thus the reflectance graph slope Gr is higher than 0.122, similarly, the effect of alleviating the interference fringe could not be obtained.
Similarly, comparing Example 1 with Comparative Example 4, it can be seen that although the first coating layer having an appropriate refractive index and thickness is applied between the second coating layer and the substrate, the effect of alleviating the interference fringe cannot be obtained when the refractive index of the first coating layer deviates from the predetermined range and thus the reflectance oscillation ratio Or is higher than 1.0.
In addition, it can be seen that, comparing Example 6 with Comparative Examples 6 and 7, when the third coating layer is formed on the other surface of the structure, to which the first coating layer having an appropriate refractive index and thickness is applied between the second coating layer and the substrate, in the case where the refractive index and thickness of the third coating layer deviate from the predetermined range and the reflectance oscillation ratio Or is higher than 1.0, the effect of improving interference fringes cannot be obtained.
In addition, as can be seen from Examples 4 and 5, when the refractive index of the substrate is changed but satisfies the predetermined range, and thus the reflectance oscillation ratio Or and the reflectance graph slope Gr satisfy the ranges of the present disclosure, an effect of alleviating the interference fringe is obtained.
In addition, as can be seen from Examples 1 and 7, the same results can be obtained even when the first coating layer composition and the second coating layer composition are not only the epoxy-based resin composition but also the acrylic-based resin composition.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2020-0076134 | Jun 2020 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2021/007679 | 6/18/2021 | WO |
