TW202407425A - Lens part and laminated film - Google Patents

Abstract

The present invention provides a lens unit that can reduce the weight of VR goggles and improve visibility. The lens unit according to the embodiment of the present invention is used in a display system that displays an image to a user. It includes a reflective polarizing member that reflects light emitted forward from the display surface of a display element that displays an image and passes through the polarizing member and the first lambda. /4 member; the first lens part is arranged on the optical path between the aforementioned display element and the aforementioned reflective polarizing member; the half-mirror is arranged between the aforementioned display element and the aforementioned first lens part. The reflecting mirror transmits the light emitted from the display element and reflects the light reflected by the reflective polarizing member toward the reflective polarizing member; the second lens part is arranged in front of the reflective polarizing member; 2nd lambda /4 member, which is arranged on the optical path between the aforementioned half-reflecting mirror and the aforementioned reflective polarizing member; and a first protective member and a second protective member, which are arranged between the aforementioned half-reflecting mirror and the aforementioned reflective polarizing member. on the optical path between them; the first protective member and the second protective member are arranged facing each other across a space; and the first protective member and the second protective member each have a wavelength in the range of 420 nm to 680 nm. The maximum value of the normal reflectance spectrum at 30° is less than 1.4%.

Description

Lens part and laminated film

The present invention relates to a lens portion and a laminated film.

Image display devices represented by liquid crystal display devices and electroluminescence (EL) display devices (such as organic EL display devices) are rapidly gaining popularity. In image display devices, in order to realize image display and improve image display performance, optical members such as polarizing members and phase difference members are generally used (for example, see Patent Document 1).

In recent years, new uses for image display devices have been developed. For example, goggles with a display (VR goggles) for realizing Virtual Reality (VR) have begun to be commercialized. There are studies on using VR goggles in various situations, so it is hoped that they can be lightweight and improve visibility. Weight reduction can be achieved, for example, by thinning the lenses used in VR goggles. On the other hand, it is also desired to develop optical components suitable for display systems using thin lenses. For example, in order to improve visibility, optical components that can solve the reflection problem that may occur in VR goggles are desired. Prior technical literature patent documents

Patent Document 1: Japanese Patent Application Publication No. 2021-103286

The problem to be solved by the invention In view of the above, the main purpose of the present invention is to provide a lens unit that can reduce the weight of VR goggles and improve visibility.

means to solve problems 1. The lens unit of the embodiment of the present invention is used in a display system that displays an image to a user. It is provided with: a reflective polarizing member that reflects light emitted forward from the display surface of the display element that displays the image and passes through the polarizing member; The light of the 1st λ/4 member; the first lens part is arranged on the optical path between the above-mentioned display element and the above-mentioned reflective polarizing member; the half-reflecting mirror is arranged between the above-mentioned display element and the above-mentioned first lens part, The half mirror transmits the light emitted from the display element and reflects the light reflected by the reflective polarizing member toward the reflective polarizing member; the second lens part is arranged in front of the reflective polarizing member; The 2λ/4 member is arranged on the optical path between the half-mirror and the reflective polarizing member; and the first protective member and the second protective member are arranged on the half-mirror and the reflective polarizing member. On the optical path between the polarizing members; the first protective member and the second protective member are arranged facing each other across a space; and the first protective member and the second protective member each have a wavelength in the range of 420 nm to 680 nm. The maximum value of the normal reflectance spectrum at 30° is less than 1.4%. 2. In the lens part as described in 1 above, the 30° normal reflectance of each of the first protective member and the second protective member at a wavelength of 450 nm may be 0.5% or less. 3. In the lens part of 1 or 2 above, the 30° normal reflectance of each of the first protective member and the second protective member at a wavelength of 600 nm may be 0.5% or less. 4. In the lens part according to any one of 1 to 3 above, the surface smoothness of each of the first protective member and the second protective member may be 0.5 arcmin or less. 5. In the lens part according to any one of the above 1 to 4, the above-mentioned 2λ/4 member may also satisfy Re(450)<Re(550). 6. The lens part according to any one of the above 1 to 5 may also be provided with: a first laminate part including the above-mentioned 2λ/4 member and the above-mentioned first protective member; and a second laminate part including the above-mentioned reflective type Polarizing member and the above-mentioned second protective member. 7. In the lens part of 6 above, the second laminate part may include an absorptive polarizing member disposed between the reflective polarizing member and the second lens part. 8. In the lens part of item 6 or 7 above, the second laminate part may include a 3λ/4 member arranged between the reflective polarizing member and the second lens part. 9. In the lens part as described in 8 above, the above-mentioned 3λ/4 member may also satisfy Re(450)<Re(550). 10. The laminated film according to the embodiment of the present invention is used in a display method having the following steps: making the light emitted through the polarizing member and the first λ/4 member to display the image pass through the half mirror and the first lens unit; The process of allowing the light passing through the 2λ/4 member to pass through the half-reflecting mirror and the first lens unit; the process of reflecting the light passing through the 2λ/4 member toward the half-reflecting mirror through the reflective polarizing member; The process of transmitting the light reflected by the polarizing member and the half mirror through the 2λ/4 member through the reflective polarizing member; and the process of allowing the light transmitted through the reflective polarizing member to pass through the second lens part; the lamination process The film is disposed on the optical path between the half mirror and the reflective polarizing member and is in contact with the space formed between the first lens part and the second lens part; and the laminated film has a wavelength of 420 nm to The maximum value of the normal reflectance spectrum at 30° in the 680nm range is less than 1.4%.

Invention effect According to the lens part of the embodiment of the present invention, VR goggles can be lightweight and improve visibility.

Embodiments of the present invention will be described below with reference to the drawings, but the present invention is not limited to these embodiments. In order to explain the drawings more clearly, the width, thickness, shape, etc. of each part may be schematically shown compared to the embodiment. However, this is only an example and is not intended to limit the interpretation of the present invention. In addition, regarding the drawings, the same or equivalent elements may be assigned the same symbols, and repeated explanations may be omitted.

(Definition of terms and symbols) The definitions of terms and symbols in this manual are as follows. (1)Refractive index (nx, ny, nz) "nx" is the refractive index in the direction where the in-plane refractive index reaches the maximum (that is, the slow axis direction), "ny" is the refractive index in the direction that is orthogonal to the slow axis in the plane (that is, the fast axis direction), and " nz" is the refractive index in the thickness direction. (2) In-plane phase difference (Re) "Re(λ)" is the in-plane phase difference measured with light of wavelength λnm at 23°C. For example, "Re(550)" is the in-plane phase difference measured using light with a wavelength of 550 nm at 23°C. Re(λ) can be calculated by the formula: Re(λ)=(nx-ny)×d when the thickness of the layer (thin film) is d(nm). (3) Phase difference in thickness direction (Rth) "Rth(λ)" is the phase difference in the thickness direction measured with light of wavelength λnm at 23°C. For example, "Rth(550)" is the phase difference in the thickness direction measured at 23°C using light with a wavelength of 550 nm. Rth(λ) can be calculated by the formula: Rth(λ)=(nx-nz)×d when the layer (film) thickness is d(nm). (4)Nz coefficient The Nz coefficient can be found by Nz=Rth/Re. (5)Angle When an angle is mentioned in this specification, the angle includes both clockwise and counterclockwise directions relative to the reference direction. So, for example, "45°" means ±45°.

FIG. 1 is a schematic diagram showing the schematic structure of a display system according to an embodiment of the present invention. FIG. 1 is a schematic diagram showing the arrangement and shape of each component of the system 2 . The display system 2 includes a display element 12 , a reflective polarizing member 14 , a first lens unit 16 , a half mirror 18 , a first phase difference member 20 , a second phase difference member 22 , and a second lens unit 24 . The reflective polarizing member 14 is disposed on the display surface 12 a side of the display element 12 , that is, in front of the display element 12 , and can reflect the light emitted from the display element 12 . The first lens portion 16 is disposed on the optical path between the display element 12 and the reflective polarizing member 14 , and the half mirror 18 is disposed between the display element 12 and the first lens portion 16 . The first phase difference member 20 is arranged on the optical path between the display element 12 and the half mirror 18 , and the second phase difference member 22 is arranged on the optical path between the half mirror 18 and the reflective polarizing member 14 .

The components arranged forward from the half mirror (in the example of the figure, the half mirror 18, the first lens part 16, the second phase difference member 22, the reflective polarizing member 14 and the second lens part 24) are: are collectively called the lens section (lens section 4).

The display element 12 is, for example, a liquid crystal display or an organic EL display, and has a display surface 12a for displaying images. The light to be emitted from the display surface 12a passes through, for example, a polarizing member (typically a polarizing film) that may be included in the display element 12 and then is emitted, becoming first linearly polarized light.

The first phase difference member 20 includes a first λ/4 member, which can convert the first linearly polarized light incident on the first phase difference member 20 into a first circularly polarized light. When the first phase difference member does not include a member other than the first λ/4 member, the first phase difference member is equivalent to the first λ/4 member. The first phase difference member 20 can also be provided on the display element 12 to be integrated.

The half mirror 18 transmits the light emitted from the display element 12 and reflects the light reflected by the reflective polarizing member 14 toward the reflective polarizing member 14 . The half-reflecting mirror 18 is integrally provided on the first lens portion 16 .

The second phase difference member 22 includes a 2λ/4 member, which allows the light reflected by the reflective polarizing member 14 and the half mirror 18 to transmit through the reflective polarizing member 14 . When the second phase difference member does not include a member other than the 2nd λ/4 member, the second phase difference member is equivalent to the 2nd λ/4 member. The second phase difference member 22 may also be provided on the first lens part 16 to be integrated.

The first circularly polarized light emitted from the 1st λ/4 member included in the first phase difference member 20 passes through the half mirror 18 and the first lens portion 16 and passes through the 2nd λ/4 member included in the second phase difference member 22 The member converts it into 2nd linearly polarized light. The second linearly polarized light emitted from the second λ/4 member is reflected toward the half mirror 18 without passing through the reflective polarizing member 14 . At this time, the polarization direction of the second linearly polarized light incident on the reflective polarizing member 14 is in the same direction as the reflection axis of the reflective polarizing member 14 . Therefore, the second linearly polarized light incident on the reflective polarizing member 14 will be reflected by the reflective polarizing member 14 .

The second linearly polarized light reflected by the reflective polarizing member 14 is converted into the second circularly polarized light by the 2λ/4 member included in the second phase difference member 22, and the second circularly polarized light emitted from the 2λ/4 member passes through The first lens portion 16 is reflected by the half mirror 18 . The second circularly polarized light reflected by the half mirror 18 passes through the first lens part 16 and is converted into the third linearly polarized light by the 2nd λ/4 member included in the second phase difference member 22 . The third linearly polarized light is transmitted through the reflective polarizing member 14 . At this time, the polarization direction of the third linearly polarized light incident on the reflective polarizing member 14 is in the same direction as the transmission axis of the reflective polarizing member 14 . Therefore, the third linearly polarized light incident on the reflective polarizing member 14 will be transmitted through the reflective polarizing member 14 .

The light from the transflective polarizing member 14 will enter the user's eyes 26 through the second lens portion 24 .

For example, the absorption axis of the polarizing member included in the display element 12 and the reflection axis of the reflective polarizing member 14 may be arranged substantially parallel to each other, or may be arranged substantially orthogonal to each other. The angle formed by the absorption axis of the polarizing member included in the display element 12 and the slow axis of the first λ/4 member included in the first phase difference member 20 is, for example, 40° to 50°, or may be 42° to 48°, or may be is about 45°. The angle formed by the absorption axis of the polarizing member included in the display element 12 and the slow axis of the 2λ/4 member included in the second phase difference member 22 is, for example, 40° to 50°, or may be 42° to 48°, or may be is about 45°.

The in-plane phase difference Re(550) of the first λ/4 member is, for example, 100nm~190nm, 110nm~180nm, 130nm~160nm, or 135nm~155nm. The first λ/4 member should preferably exhibit inverse dispersion wavelength characteristics in which the phase difference value increases with the wavelength of the measurement light. Re(450)/Re(550) of the first λ/4 member is, for example, 0.75 or more and less than 1, or may be 0.8 or more and 0.95 or less.

The in-plane phase difference Re(550) of the 2nd λ/4 member is, for example, 100nm~190nm, 110nm~180nm, 130nm~160nm, or 135nm~155nm. The 2λ/4 member should preferably exhibit inverse dispersion wavelength characteristics in which the phase difference value increases with the wavelength of the measurement light. Re(450)/Re(550) of the second λ/4 member is, for example, 0.75 or more and less than 1, or may be 0.8 or more and 0.95 or less.

In the lens part 4, a space may be formed between the first lens part 16 and the second lens part 24. At this time, it is preferable that the member arranged between the first lens part 16 and the second lens part 24 is provided integrally with any one of the first lens part 16 and the second lens part 24 . For example, it is preferable that the member disposed between the first lens portion 16 and the second lens portion 24 is integrally provided on either the first lens portion 16 or the second lens portion 24 through an adhesive layer. According to this aspect, for example, each member can be made to have excellent handling properties. The following layer may be formed of an adhesive or an adhesive. Specifically, the bonding layer may be an adhesive layer or an adhesive layer. The thickness of the subsequent layer is, for example, 0.05µm~30µm.

FIG. 2 is a schematic cross-sectional view showing an example of details of the lens portion of the display system shown in FIG. 1 . Specifically, FIG. 2 shows a first lens part, a second lens part, and members arranged between them. The lens portion 4 includes a first lens portion 16 , a first laminate portion 100 adjacent to the first lens portion 16 , a second lens portion 24 , and a second laminate portion 200 adjacent to the second lens portion 24 . In the example shown in FIG. 2 , the first lamination part 100 and the second lamination part 200 are arranged separately. Although not shown in the figure, the half mirror may be integrally provided on the first lens part 16 .

The first laminate part 100 includes the second phase difference member 22 and an adhesive layer (for example, an adhesive layer) 41 disposed between the first lens part 16 and the second phase difference member 22. The adhesive layer 41 is provided on the second phase difference member 22. A lens part 16 is integrated. The first lamination part 100 further includes a first protection member 31 arranged in front of the second phase difference member 22 . The first protective member 31 is laminated on the second phase difference member 22 through an adhesive layer (eg, adhesive layer) 42 . The first protective member 31 may be located on the outermost surface of the first laminate part 100 .

In the example shown in FIG. 2 , the second phase difference member 22 includes, in addition to the second λ/4 member 22 a , a member (so-called positive C plate) 22 b whose refractive index characteristics exhibit the relationship nz>nx=ny. The second phase difference member 22 has a laminated structure of the second λ/4 member 22a and the positive C plate 22b. By using a positive C plate, light leakage (such as oblique light leakage) can be prevented. As shown in FIG. 2 , among the second phase difference members 22 , the second λ/4 member 22 a is preferably located further forward than the front C plate 22 b. The second λ/4 member 22a and the positive C plate 22b are laminated via an adhesive (not shown), for example.

It is preferable that the refractive index characteristics of the above-mentioned 2λ/4 member show the relationship nx>ny≧nz. Here "ny=nz" includes not only the case where ny and nz are exactly the same, but also the case where they are substantially the same. Therefore, ny<nz may be satisfied as long as the effect of the present invention is not impaired. The Nz coefficient of the 2nd λ/4 member is preferably 0.9~3, more preferably 0.9~2.5, more preferably 0.9~1.5, especially 0.9~1.3.

The 2λ/4 member is formed of any suitable material that can satisfy the above characteristics. The 2 λ/4 member may be, for example, a stretched film of a resin film or a directionally solidified layer of a liquid crystal compound.

Examples of the resin contained in the above-mentioned resin film include polycarbonate resin, polyester carbonate resin, polyester resin, polyvinyl acetal resin, polyarylate resin, cyclic olefin resin, and cellulose resin. Resin, polyvinyl alcohol resin, polyamide resin, polyimide resin, polyether resin, polystyrene resin, acrylic resin, etc. These resins can be used individually or in combination. Examples of the combination method include blending and copolymerization. When the 2 λ/4 member exhibits reverse dispersion wavelength characteristics, a resin film containing polycarbonate resin or polyester carbonate resin (hereinafter sometimes simply referred to as polycarbonate resin) can be suitably used.

Any appropriate polycarbonate resin can be used as the polycarbonate resin. For example, the polycarbonate resin includes: a structural unit derived from a fluorine-based dihydroxy compound; a structural unit derived from an isosorbide-based dihydroxy compound; and a structural unit derived from an alicyclic diol, an alicyclic diol, or an alicyclic diol. The structural unit of at least one dihydroxy compound in the group consisting of dimethanol, di, tri or polyethylene glycol, and alkylene glycol or spiroglycerol. The polycarbonate resin preferably contains: a structural unit derived from a fluorine-based dihydroxy compound; a structural unit derived from an isosorbide-based dihydroxy compound; a structural unit derived from an alicyclic dimethanol; and/or derived from Structural units of di, tri or polyethylene glycol; more preferably include: structural units derived from fluorine series dihydroxy compounds; structural units derived from isosorbide series dihydroxy compounds; and, derived from di, tri or polyethylene glycol. The structural unit of ethylene glycol. The polycarbonate resin may also contain structural units derived from other dihydroxy compounds if necessary. In addition, details of a polycarbonate-based resin suitably used for the 2λ/4 member and a method for forming the 2λ/4 member are described in, for example, Japanese Patent Laid-Open No. 2014-10291 and Japanese Patent Laid-Open No. 2014-26266 Publication No. 2015-212816, Japanese Patent Application Publication No. 2015-212817, and Japanese Patent Application Publication No. 2015-212818, the descriptions of these publications are incorporated into this specification as a reference.

The thickness of the 2nd λ/4 member made of a stretched film of a resin film is, for example, 10µm~100µm, preferably 10µm~70µm, more preferably 20µm~60µm.

The orientation-solidified layer of the above-mentioned liquid crystal compound is a layer in which the liquid crystal compound is oriented in a predetermined direction within the layer and its orientation state is fixed. In addition, the concept of "directionally hardened layer" includes a directionally hardened layer obtained by hardening a liquid crystal monomer as described later. Taking the 2λ/4 member as an example, it means that the rod-shaped liquid crystal compounds are aligned along the slow axis direction of the 2λ/4 member and are oriented (elevated along the surface). Examples of rod-shaped liquid crystal compounds include liquid crystal polymers and liquid crystal monomers. The liquid crystal compound is preferably polymerizable. If the liquid crystal compound is polymerizable, the liquid crystal compound can be polymerized after alignment, thereby fixing the alignment state of the liquid crystal compound.

The directionally solidified layer of the above-mentioned liquid crystal compound (liquid crystal directionally solidified layer) can be formed by subjecting the surface of a predetermined base material to an orientation treatment, and applying a coating liquid containing a liquid crystal compound to the surface, so that the liquid crystal compound Orient in the direction corresponding to the above orientation processing, and fix the orientation state. The directional treatment may employ any suitable directional treatment. Specifically, mechanical orientation treatment, physical orientation treatment, and chemical orientation treatment can be cited. Specific examples of mechanical orientation treatment include friction treatment and stretching treatment. Specific examples of physical orientation processing include magnetic field orientation processing and electric field orientation processing. Specific examples of chemical orientation treatment include oblique evaporation and photo-orientation treatment. The processing conditions for various targeted treatments can be any appropriate conditions depending on the purpose.

The orientation of the liquid crystal compound can be carried out by treating the liquid crystal compound at a temperature that can exhibit a liquid crystal phase according to the type of the liquid crystal compound. By performing the temperature treatment, the liquid crystal compound will change into a liquid crystal state, and the liquid crystal compound will be oriented according to the direction of the orientation treatment on the surface of the substrate.

In one embodiment, the alignment state is fixed by cooling the liquid crystal compound aligned in the above manner. When the liquid crystal compound is polymerizable or cross-linked, the alignment state is fixed by subjecting the liquid crystal compound oriented in the above manner to polymerization treatment or cross-linking treatment.

Any appropriate liquid crystal polymer and/or liquid crystal monomer may be used as the above liquid crystal compound. The liquid crystal polymer and the liquid crystal monomer can each be used alone or in combination. Specific examples of the liquid crystal compound and methods of producing the liquid crystal alignment solidified layer are described in, for example, Japanese Patent Laid-Open No. 2006-163343, Japanese Patent Laid-Open No. 2006-178389, and International Publication No. 2018/123551. This manual refers to the records in these publications as a reference.

The thickness of the 2λ/4 member composed of the liquid crystal orientation solidified layer is, for example, 1µm~10µm, preferably 1µm~8µm, more preferably 1µm~6µm, and more preferably 1µm~4µm.

The phase difference Rth (550) in the thickness direction of the above-mentioned positive C plate is preferably -50nm~-300nm, more preferably -70nm~-250nm, more preferably -90nm~-200nm, especially -100nm~-180nm. Here, "nx=ny" includes not only the case where nx and ny are strictly equal, but also the case where nx and ny are substantially equal. The in-plane phase difference Re (550) of the positive C plate is, for example, less than 10 nm.

The positive C plate can be formed of any suitable material, and the positive C plate is preferably composed of a film containing a liquid crystal material fixed in a vertical orientation. The liquid crystal material (liquid crystal compound) capable of vertical alignment can be a liquid crystal monomer or a liquid crystal polymer. Specific examples of the method of forming the liquid crystal compound and the positive C plate include the method of forming the liquid crystal compound and the retardation layer described in paragraphs [0020] to [0028] of Japanese Patent Application Laid-Open No. 2002-333642. At this time, the thickness of the positive C plate should be 0.5µm~5µm.

Typically, the first protective member may be a laminated film having a base material and a surface treatment layer. The first protective member having the surface treatment layer may be configured such that the surface treatment layer is located on the front side. Specifically, the surface treatment layer may be located on the outermost surface of the first build-up part.

The maximum value of the 30° normal reflectance spectrum of the first protective member in the wavelength range of 420 nm to 680 nm is 0% or more and 1.4% or less, preferably 1.2% or less, more preferably 1.0% or less. By locating the protective member having the reflective characteristics on the outermost surface of the laminated part, visibility can be particularly improved. Specifically, since the protective member in contact with the space formed between the first lens portion 16 and the second lens portion 24 satisfies the above-mentioned reflection characteristics, it is possible to extremely effectively suppress the reflection caused by the interface between the air and the protective member. light loss. Specifically, light is diffused in the display system 2, and the diffused light may be incident on the protective member from an oblique direction. The optical loss can be suppressed extremely well. In the display system 2 using a large number of components, a large amount of light is required, so that the effect of suppressing light loss can be significantly obtained. As described above, in the display system 2 shown in FIG. 1 , since light can pass through the member disposed between the half mirror 18 and the reflective polarizing member 14 three times, the effect of suppressing light loss can be significantly obtained. In addition, since the protective member satisfies the above-mentioned reflection characteristics, it is possible to suppress ghosts from being visually recognized due to reflection.

As mentioned above, hue management is very important when using a large amount of light. For example, the balance of reflectivity in the visible light region is important. The 30° normal reflectance of the first protective member at a wavelength of 450 nm is, for example, 0.01% or more and 0.6% or less, preferably 0.5% or less, more preferably 0.4% or less, and more preferably 0.3% or less. The 30° normal reflectance of the first protective member at a wavelength of 600 nm is, for example, 0.01% or more and 0.6% or less, preferably 0.5% or less, more preferably 0.4% or less, and more preferably 0.3% or less.

The 30° normal reflectance spectrum of the first protective member in the wavelength range of 420 nm to 680 nm may also have a minimum value in the wavelength range of 430 nm to 470 nm and in the wavelength range of 550 nm to 590 nm. For example, the ratio of the average Ave (430-470nm) of the 30° normal reflectance in the wavelength range of 430nm to 470nm relative to the average Ave (480-510nm) of the 30° normal reflectance in the wavelength range of 480nm to 510nm It is suitable to be above 0.10 and below 1.0, and may be below 0.80. Moreover, the ratio of the average value Ave (580-620nm) of the 30° normal reflectance in the wavelength range of 580nm to 620nm relative to the average value Ave (480-510nm) of the 30° normal reflectance in the wavelength range 480nm to 510nm It is suitable to be above 0.10 and below 1.0, and may be below 0.80. In addition, the average value of the 30° normal reflectance can be obtained, for example, by selecting measured values every 5 nm in each wavelength range and dividing the total by the number of extracted wavelengths.

The surface smoothness of the first protective member is preferably 0.5 arcmin or less, more preferably 0.4 arcmin or less. By using a protective member that satisfies the above-mentioned smoothness, the occurrence of diffuse light can be suppressed, and the image can be suppressed from becoming unclear. In essence, the surface smoothness of the first protective member is, for example, 0.1 arcmin or more. The thickness of the first protective component is preferably 10µm~80µm, more preferably 15µm~60µm, and more preferably 20µm~45µm.

FIG. 3 is a schematic cross-sectional view showing the schematic structure of a laminated film according to an embodiment of the present invention. The laminated film 34 has a base material 36 and a surface treatment layer 38 arranged above the base material 36 . The thickness of the substrate 36 is preferably 5µm~80µm, more preferably 10µm~50µm, more preferably 15µm~40µm. The surface smoothness of the base material 36 is preferably 0.7 arcmin or less, more preferably 0.6 arcmin or less, and more preferably 0.5 arcmin or less. In addition, surface smoothness can be measured by focusing illumination light on the surface of the object.

The substrate 36 can be made of any suitable film. Examples of materials that constitute the main component of the film constituting the base material 36 include cellulose-based resins such as triacetylcellulose (TAC), polyester-based, polyvinyl alcohol-based, polycarbonate-based, polyamide-based, polyamide-based resins, etc. Resins of imine series, polyether series, polystyrene series, polystyrene series, polynorphenyl series, cycloolefin series, polyolefin series, (meth)acrylic series and acetate series, etc. Here, (meth)acrylic acid means acrylic acid and/or methacrylic acid. In one embodiment, the base material 36 is preferably made of (meth)acrylic resin. By using (meth)acrylic resin, the above-mentioned surface smoothness can be satisfactorily satisfied. Specifically, by using (meth)acrylic resin, a base material with excellent surface smoothness can be produced by extrusion molding.

The thickness of the surface treatment layer 38 is preferably 0.5µm~10µm, more preferably 1µm~7µm, and more preferably 2µm~5µm. The surface treatment layer 38 includes, for example, a hard coat layer 38a and a functional layer 38b with an anti-reflective function.

The hard coat layer 38a is typically formed by applying a hard coat layer-forming material to the base material 36 and hardening the coating layer. The hard coat layer forming material typically contains a curable compound as a layer forming component. Examples of the curing mechanism of the curable compound include thermosetting type and photocuring type. Examples of the curable compound include monomers, oligomers, and prepolymers. Preferably, polyfunctional monomers or oligomers can be used as the curing compound. Examples of polyfunctional monomers or oligomers include monomers or oligomers having two or more (meth)acrylyl groups, urethane (meth)acrylate, or urethane (meth)acrylic acid. Ester oligomers, epoxy monomers or oligomers, polysiloxane monomers or oligomers.

The thickness of the hard coating layer 38a is preferably 0.5µm~10µm, more preferably 1µm~7µm, and more preferably 2µm~5µm.

The functional layer 38b preferably has a laminated structure including a high refractive index layer and a low refractive index layer. It is preferable that the functional layer 38b has a high refractive index layer and a low refractive index layer in order from the base material 36 side. By having the above-described laminated structure, the above-mentioned reflection characteristics can be satisfactorily satisfied.

For example, the above-mentioned high refractive index layer can be composed of a high refractive index resin (for example, the refractive index measured under the condition of a wavelength of 550 nm is 1.55 or more). At this time, the high refractive index layer may be represented by a coating layer. For another example, the above-mentioned high refractive index layer may be composed of an inorganic film. At this time, the high refractive index layer can be formed by physical evaporation or chemical evaporation such as vacuum evaporation and sputtering.

The thickness of the high refractive index layer is preferably 10nm~200nm, more preferably 20nm~150nm.

The thickness of the low refractive index layer is preferably 10nm~200nm, more preferably 20nm~150nm.

The low refractive index layer (antireflection layer) can be obtained, for example, by hardening a coating film obtained by applying a coating liquid for forming a low refractive index layer (antireflection layer) and drying it. The coating liquid for forming the antireflection layer may also contain, for example, a resin component (hardening compound), a fluorine-containing additive, hollow particles, solid particles, a solvent, etc., and may be obtained by mixing them, for example.

Examples of the curing mechanism of the resin component (curable compound) contained in the antireflection layer-forming coating liquid include thermosetting type and photocuring type. As the resin component, for example, a curable compound having at least one of an acrylate group and a methacrylate group can be used, and examples thereof include polysilicone resin, polyester resin, polyether resin, epoxy resin, and urethane. Resins, alkyd resins, spiroacetal resins, polybutadiene resins, polythiol polyene resins, acrylates or methacrylates and other oligomers or prepolymers of polyfunctional compounds such as polyols, etc. These may be used individually by 1 type or in combination of 2 or more types.

For example, a reactive diluent having at least one of an acrylate group and a methacrylate group can be used in the above-mentioned resin component. The reactive diluent described in Japanese Patent Application Laid-Open No. 2008-88309 can be used, for example, including monofunctional acrylate, monofunctional methacrylate, multifunctional acrylate, multifunctional methacrylate, etc. . From the viewpoint of obtaining excellent hardness, it is preferable to use a trifunctional or higher functional acrylate or a trifunctional or higher functional methacrylate as the reactive diluent. Examples of the reactive diluent include butanediol glyceryl ether diacrylate, isocyanuric acid acrylate, isocyanuric acid methacrylate, and the like. These may be used individually by 1 type or in combination of 2 or more types. In order to harden the above-mentioned resin component, a hardener may also be used, for example. As the curing agent, for example, a known polymerization initiator (such as a thermal polymerization initiator, a photopolymerization initiator, etc.) can be used.

The above-mentioned fluorine-containing additive may be, for example, a fluorine-containing organic compound or a fluorine-containing inorganic compound. Examples of fluorine-containing organic compounds include fluorine-containing antifouling coating agents, fluorine-containing acrylic compounds, and fluorine-containing and silicon-containing acrylic compounds. Commercially available fluorine-containing organic compounds can be used. Specific examples of commercially available products include the trade name "KY-1203" manufactured by Shin-Etsu Chemical Industry Co., Ltd., the trade name "MEGAFACE" manufactured by DIC Co., Ltd., and the like. The content of the fluorine-containing additive may be, for example, 0.05 parts by weight or more, 0.1 parts by weight or more, 0.15 parts by weight or more, 0.20 parts by weight or more, or 0.25 parts by weight or more, and may be 20 parts by weight or less, relative to 100 parts by weight of the above-mentioned resin component. 15 parts by weight or less, 10 parts by weight or less, 5 parts by weight or less, or 3 parts by weight or less.

Examples of the hollow particles include silica particles, acrylic particles, and acrylic-styrene copolymer particles. Commercially available hollow silica particles can be used (for example, trade names "THRULYA 5320" and "THRULYA 4320" manufactured by Nippon Chemical Industry Co., Ltd.). The weight average particle diameter of the hollow particles may be, for example, 30 nm or more, 40 nm or more, 50 nm or more, 60 nm or more, or 70 nm or more, or 150 nm or less, 140 nm or less, 130 nm or less, 120 nm or less, or 110 nm or less. The shape of the hollow particles is not particularly limited, but is preferably approximately spherical. Specifically, the aspect ratio of the hollow particles is preferably 1.5 or less. The content of the hollow particles may be, for example, 30 parts by weight or more, 50 parts by weight or more, 70 parts by weight or more, 90 parts by weight or more, or 100 parts by weight or more relative to 100 parts by weight of the above resin component, or it may be 300 parts by weight or less, 270 parts by weight or less. Parts by weight or less, 250 parts by weight or less, 200 parts by weight or less, or 180 parts by weight or less.

Examples of the solid particles include silicon oxide particles, zirconium oxide particles, and titanium oxide particles. Commercially available solid silicon oxide particles can be used (for example, trade names "MEK-2140Z-AC", "MIBK-ST", and "IPA-ST" manufactured by Nissan Chemical Industries, Ltd.). The weight average particle diameter of the solid particles may be, for example, 5 nm or more, 10 nm or more, 15 nm or more, 20 nm or more, or 25 nm or more, and may be 330 nm or less, 250 nm or less, 200 nm or less, 150 nm or less, or 100 nm or less. The shape of the hollow particles is not particularly limited, but is preferably approximately spherical. Specifically, the aspect ratio of the hollow particles is preferably 1.5 or less. The content of the solid particles may be, for example, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, or 25 parts by weight or more relative to 100 parts by weight of the above-mentioned resin component, or it may be 150 parts by weight or less, 120 parts by weight or less. Parts by weight or less, 100 parts by weight or less, or 80 parts by weight or less.

Any suitable solvent may be used as the above solvent. Examples of the solvent include alcohols such as methanol, ethanol, isopropyl alcohol, butanol, TBA (tertiary butanol), and 2-methoxyethanol; acetone, methyl ethyl ketone, and MIBK (methyl isobutyl ketone) , cyclopentanone and other ketones; esters such as methyl acetate, ethyl acetate, butyl acetate, PMA (propylene glycol monomethyl ether acetate); ethers such as diisopropyl ether, propylene glycol monomethyl ether; Glycols such as ethylene glycol and propylene glycol; cellulosoids such as cellulosine and cellulose; aliphatic hydrocarbons such as hexane, heptane and octane; aromatic hydrocarbons such as benzene, toluene and xylene. These may be used individually by 1 type or in combination of 2 or more types. The content of the solvent may be, for example, 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 1.0% by weight or more based on the weight of the solid content of the entire coating liquid for forming an antireflection layer. 1.5% by weight or more, and the weight of the solid content may be 20% by weight or less, 15% by weight or less, 10% by weight or less, 5% by weight or less, or 3% by weight or less.

The above-mentioned coating liquid for forming the anti-reflection layer can be applied by any known coating method such as injection coating, die coating, spin coating, spray coating, gravure coating, roller coating, rod coating, etc. Application method. The drying temperature of the coating film is, for example, 30°C to 200°C, and the drying time is, for example, 30 seconds to 90 seconds. The coating film can be cured by, for example, heating or light irradiation (typically ultraviolet irradiation). As a light source for light irradiation, a high-pressure mercury lamp can be used, for example. The amount of ultraviolet irradiation is preferably 50mJ/cm ² ~500mJ/cm ² in terms of the cumulative exposure under the ultraviolet wavelength of 365nm.

The second laminate part 200 includes the reflective polarizing member 14 and an adhesive layer (for example, an adhesive layer) disposed between the reflective polarizing member 14 and the second lens part 24 . For example, from the perspective of improving visibility, the second laminate part 200 further includes an absorptive polarizing member 28 disposed between the reflective polarizing member 14 and the second lens part 24 . The absorptive polarizing member 28 is laminated in front of the reflective polarizing member 14 through an adhesive layer (eg, adhesive layer) 44 . The reflection axis of the reflective polarizing member 14 and the absorption axis of the absorptive polarizing member 28 may be arranged substantially parallel to each other, and the transmission axis of the reflective polarizing member 14 and the absorptive polarizing member 28 may be arranged substantially parallel to each other. By adhering to the lamination layer, the reflective polarizing member 14 and the absorbing polarizing member 28 are fixed, thereby preventing misalignment of the reflection axis and the absorption axis (the transmission axis and the transmission axis). In addition, adverse effects caused by the air layer that may be formed between the reflective polarizing member 14 and the absorbing polarizing member 28 can be suppressed.

The second lamination part 200 further includes a second protective member 32 disposed behind the reflective polarizing member 14 . The second protective member 32 is laminated on the reflective polarizing member 14 through an adhesive layer (such as an adhesive layer) 43 . The second protection member 32 may be located on the outermost surface of the second laminate part 200 . The first protective member 31 and the second protective member 32 are arranged to face each other across a space. Like the above-mentioned first protective member, the second protective member can typically be a laminated film having a base material and a surface treatment layer. At this time, the surface treatment layer may be located on the outermost surface of the second build-up part. Regarding the details of the second protective member, the same description as for the above-mentioned first protective member can be applied. Specifically, the same description as that of the above-mentioned first protective member can be applied regarding the reflective characteristics, effects, smoothness, composition, thickness, and constituent materials of the second protective member.

In the example shown in FIG. 2 , the second laminate part 200 further includes a third phase difference member 30 disposed between the absorptive polarizing member 28 and the second lens part 24 . The third phase difference member 30 is laminated on the absorptive polarizing member 28 through an adhesive layer (such as an adhesive layer) 45 . In addition, the third phase difference member 30 is laminated on the second lens part 24 through the adhesive layer (eg, adhesive layer) 46, and the second laminated part 200 is provided on the second lens part 24 to be integrated. The third phase difference member 30 includes, for example, a third λ/4 member. The angle formed by the absorption axis of the absorptive polarizing member 28 and the slow axis of the 3λ/4 member included in the third phase difference member 30 is, for example, 40°~50°, 42°~48°, or about 45°. °. By providing such a member, it is possible to prevent reflection of light from outside the second lens portion 16 side, for example. When the third phase difference member does not include a member other than the 3λ/4 member, the third phase difference member is equivalent to the 3λ/4 member.

The reflective polarizing member can transmit polarized light parallel to its transmission axis (typically linear polarization) while maintaining its polarized state, and can reflect light in other polarized states. Reflective polarizing components are typically composed of films with a multi-layer structure (sometimes called reflective polarizing films). At this time, the thickness of the reflective polarizing member is, for example, 10µm~150µm, preferably 20µm~100µm, and more preferably 30µm~60µm.

FIG. 4 is a schematic perspective view showing an example of a multi-layer structure included in a reflective polarizing film. The multilayer structure 14 a alternately has a birefringent layer A and a substantially non-birefringent layer B. The total number of layers constituting the multi-layer structure can also be 50~1000. For example, the refractive index nx of layer A in the x-axis direction is greater than the refractive index ny in the y-axis direction, and the refractive index nx of layer B in the x-axis direction is substantially the same as the refractive index ny in the y-axis direction; on the x-axis The refractive index difference between layer A and layer B is large in the direction, and is essentially zero in the y-axis direction. As a result, the x-axis direction will become the reflection axis, and the y-axis direction will become the transmission axis. The refractive index difference between layer A and layer B in the x-axis direction should be 0.2~0.3.

The above-mentioned A layer is typically made of a material that exhibits birefringence through extension. Examples of the material include naphthalenedicarboxylic acid polyester (such as polyethylene naphthalate), polycarbonate and acrylic resin (such as polymethyl methacrylate). The B layer is typically made of a material that does not exhibit substantial birefringence even when stretched. Examples of the material include copolyesters of naphthalenedicarboxylic acid and terephthalic acid. The above-mentioned multi-layer structure can be formed by a combination of co-extrusion and stretching. For example, the material constituting layer A and the material constituting layer B are extruded and then multi-layered (for example, using a multiplier). Next, the obtained multi-layered laminate is stretched. The x-axis direction of the diagram example can correspond to the extension direction.

Commercially available reflective polarizing films include, for example, the trade names "DBEF" and "APF" manufactured by 3M Company, and the trade name "APCF" manufactured by Nitto Denko Corporation.

The cross transmittance (Tc) of the reflective polarizing member (reflective polarizing film) can be, for example, 0.01%~3%. The single transmittance (Ts) of the reflective polarizing member (reflective polarizing film) is, for example, 43% to 49%, preferably 45% to 47%. The polarization degree (P) of the reflective polarizing member (reflective polarizing film) can be, for example, 92% to 99.99%.

The above-mentioned orthogonal transmittance, single transmittance, and polarization degree can be measured using an ultraviolet-visible light spectrophotometer, for example. The degree of polarization P can be measured using an ultraviolet-visible light spectrophotometer to measure the single transmittance Ts, the parallel transmittance Tp, and the orthogonal transmittance Tc, and calculate it from the obtained Tp and Tc using the following formula. In addition, Ts, Tp and Tc are Y values measured using the 2-degree visual field (C light source) of JIS Z 8701 and corrected for visual sensitivity. Polarization P(%)={(Tp-Tc)/(Tp+Tc)} ^1/2 ×100

The above-mentioned absorptive polarizing member may typically include a resin film containing a dichroic substance (sometimes referred to as an absorptive polarizing film). The thickness of the absorptive polarizing film may be, for example, 1 µm or more and 20 µm or less, 2 µm or more and 15 µm or less, 12 µm or less, 10 µm or less, 8 µm or less, or 5 µm or less.

The above-mentioned absorptive polarizing film can be made of a single-layer resin film or a laminate of two or more layers.

When made from a single-layer resin film, for example, hydrophilic polymer films such as polyvinyl alcohol (PVA)-based films, partially formalized PVA-based films, and ethylene vinyl acetate copolymer-based partially saponified films can be processed. Dyeing treatment, stretching treatment, etc. using dichroic substances such as iodine or dichroic dyes are used to obtain an absorptive polarizing film. Among them, an absorption-type polarizing film obtained by dyeing a PVA-based film with iodine and uniaxially stretching it is preferred.

The above-described dyeing with iodine can be performed, for example, by immersing a PVA-based film in an iodine aqueous solution. The extension ratio of the above-mentioned uniaxial extension is preferably 3 to 7 times. Extending can be done after dyeing or while dyeing. Also, it can be dyed after stretching. If necessary, the PVA film is subjected to swelling treatment, cross-linking treatment, washing treatment, drying treatment, etc.

Examples of the laminated body when produced using the above-mentioned two or more laminated bodies include the following laminated bodies: a laminated body of a resin base material and a PVA-based resin layer (PVA-based resin film) laminated on the resin base material; or a resin-based laminated body. A laminate consisting of a material and a PVA-based resin layer coated on the resin base material. An absorption-type polarizing film using a laminate of a resin base material and a PVA-based resin layer coated on the resin base material can be produced, for example, by the following steps: applying a PVA-based resin solution to the resin base material and dry it to form a PVA-based resin layer on the resin base material to obtain a laminated body of the resin base material and the PVA-based resin layer; and stretch and dye the laminated body to form the PVA-based resin layer into an absorbing polarizing film . In this embodiment, it is preferable to form a polyvinyl alcohol-based resin layer containing a halide and a polyvinyl alcohol-based resin on one side of the resin base material. Stretching typically includes immersing the laminate in a boric acid aqueous solution to stretch. And if necessary, stretching may further include stretching the laminate in the air at a high temperature (for example, above 95° C.) before stretching in a boric acid aqueous solution. Furthermore, in this embodiment, it is preferable to subject the laminated body to a drying and shrinking process in which the laminated body is heated while being conveyed in the longitudinal direction to shrink the laminated body by 2% or more in the width direction. Typically, the manufacturing method of this embodiment includes sequentially performing an air-assisted stretching process, a dyeing process, an underwater stretching process, and a drying shrinkage process on the laminate. By introducing auxiliary stretching, the crystallinity of PVA can be improved even when PVA is coated on thermoplastic resin, and high optical properties can be achieved. In addition, by improving the orientation of PVA in advance, it can prevent problems such as reduction in orientation or dissolution of PVA when immersed in water in the subsequent dyeing step or stretching step, thereby achieving high optical properties. In addition, when the PVA-based resin layer is immersed in a liquid, compared with the case where the PVA-based resin layer does not contain halides, the orientation disorder and decrease in orientation of polyvinyl alcohol molecules can be suppressed. Thereby, the optical characteristics of the absorptive polarizing film obtained by immersing the laminate in a liquid, such as dyeing treatment and water stretching treatment, can be improved. In addition, the optical properties can be improved by shrinking the laminate in the width direction through drying and shrinkage treatment. The obtained laminate of the resin base material/absorptive polarizing film can be used directly (that is, the resin base material can be used as a protective layer of the absorptive polarizing film), or the resin can be peeled off from the laminate of the resin base material/absorptive polarizing film. Use any suitable protective layer that meets the purpose on the peeling surface behind the base material or on the area opposite to the peeling surface. Details of the manufacturing method of the absorptive polarizing film are described in, for example, Japanese Patent Application Laid-Open No. 2012-73580 and Japanese Patent No. 6470455. The entire description of these publications is cited in this specification as a reference.

The cross transmittance (Tc) of the absorptive polarizing member (absorbent polarizing film) is preferably 0.5% or less, more preferably 0.1% or less, and more preferably 0.05% or less. The single transmittance (Ts) of the absorptive polarizing member (absorptive polarizing film) is, for example, 41.0% to 45.0%, preferably 42.0% or more. The degree of polarization (P) of the absorptive polarizing member (absorptive polarizing film) is, for example, 99.0% to 99.997%, preferably 99.9% or more.

The in-plane phase difference Re(550) of the above-mentioned third λ/4 member is, for example, 100nm~190nm, may be 110nm~180nm, may be 130nm~160nm, or may be 135nm~155nm. The 3λ/4 member should preferably exhibit inverse dispersion wavelength characteristics in which the phase difference value increases with the wavelength of the measurement light. Re(450)/Re(550) of the third λ/4 member is, for example, 0.75 or more and less than 1, or may be 0.8 or more and 0.95 or less. The 3λ/4 member should preferably exhibit the relationship nx>ny≧nz for its refractive index characteristics. The Nz coefficient of the third λ/4 member should be 0.9~3, more preferably 0.9~2.5, more preferably 0.9~1.5, especially 0.9~1.3.

The 3λ/4 member is formed of any suitable material that can satisfy the above characteristics. The 3λ/4 member may be, for example, a stretched film of a resin film or a directionally solidified layer of a liquid crystal compound. Regarding the third λ/4 member composed of a stretched film of a resin film or an orientationally solidified layer of a liquid crystal compound, the same description as that of the above-mentioned 2λ/4 member can be applied. The 2nd λ/4 member and the 3rd λ/4 member may have the same structure (for example, formation material, thickness, optical properties, etc.), or may have different structures.

Example Hereinafter, the present invention will be specifically described through examples, but the present invention is not limited by these examples. In addition, thickness and surface smoothness are values measured by the following measurement methods. In addition, unless otherwise stated, "parts" and "%" are based on weight. ＜Thickness＞ The thickness of 10 µm or less is measured using a scanning electron microscope (manufactured by JEOL Ltd., product name "JSM-7100F"). Thickness greater than 10µm is measured using a digital micrometer (manufactured by Anritsu Co., Ltd., product name "KC-351C"). ＜Surface Smoothness＞ Measurement was performed using a scanning white interferometer (manufactured by Zygo, product name "NewView9000"). Specifically, the measurement sample is placed on a measurement table with an anti-vibration table, a single white LED is used to illuminate the interference fringes, and an interference objective lens (1.4 times) with a reference plane is scanned in the Z direction (thickness direction). Selectively obtains the smoothness (surface smoothness) of the outermost surface of the measurement object within a field of view of 12.4mm□. An acrylic adhesive layer with a thickness of 5 µm and less unevenness is formed on a slide glass (manufactured by Matsunami Glass Industry Co., Ltd., product name "S200200"), and the object to be measured is placed in such a way that foreign matter, air bubbles, and deformed streaks are not allowed to enter. The film is laminated on the adhesive surface, and the smoothness of the surface opposite to the adhesive layer is measured. Regarding analysis, the value obtained by multiplying the angle index "Slope magnitude RMS" by 2 times (equivalent to 2σ) is defined as surface smoothness (unit: arcmin).

[Example 1] (Preparation of hard coat forming materials) 50 parts of mixed urethane acrylate oligomer (manufactured by Shin-Nakamura Chemical Co., Ltd., "NK Oligo UA-53H"), multifunctional acrylate mainly composed of neopentylerythritol triacrylate (Osaka Organic Chemical Industry Co., Ltd. (made under the trade name "Viscoat #300"), 30 parts of 4-hydroxybutyl acrylate (manufactured by Osaka Organic Chemical Industry Co., Ltd.), 1 part of leveling agent (manufactured by DIC Corporation, "GRANDIC PC4100") and photopolymerization initiator ("IRGACURE 907" manufactured by Ciba Japan Co., Ltd.) and diluted with methyl isobutyl ketone so that the solid content concentration became 50%, to prepare a hard coating forming material.

(Preparation of coating liquid for high refractive index layer formation) Mix 100 parts by weight of polyfunctional acrylate (manufactured by Arakawa Chemical Industry Co., Ltd., trade name "OPSTAR KZ6728", solid content 20% by weight), 3 parts by weight of leveling agent (manufactured by DIC Corporation, "GRANDIC PC4100") and photopolymerization initiator agent (manufactured by BASF, trade name "OMNIRAD907", solid content 100% by weight) 3 parts by weight. In this mixture, butyl acetate was used as a diluent solvent so that the solid content became 12% by weight, and the mixture was stirred to prepare a coating liquid for forming a high refractive index layer.

(Preparation of coating liquid A for forming low refractive index layer) Mix 100 parts by weight of polyfunctional acrylate containing neopentyl erythritol triacrylate as the main component (manufactured by Osaka Organic Chemical Industry Co., Ltd., trade name "Viscoat #300", solid content 100% by weight), and hollow nanosilica Particles (manufactured by Nissan Chemical Industry Co., Ltd., trade name "THRULYA 5320", solid content 20% by weight, weight average particle diameter 75 nm) 150 parts by weight, solid nanosilica particles (manufactured by Nissan Chemical Industry Co., Ltd., product Name "MEK-2140Z-AC", solid content 30% by weight, weight average particle size 10 nm) 50 parts by weight, fluorine-containing additive (manufactured by Shin-Etsu Chemical Industry Co., Ltd., trade name "KY-1203", solid content 20% by weight) 12 parts by weight and 3 parts by weight of a photopolymerization initiator (manufactured by BASF, trade name "OMNIRAD907", solid content: 100% by weight). To this mixture, a mixed solvent of TBA (tertiary butanol), MIBK (methyl isobutyl ketone) and PMA (propylene glycol monomethyl ether acetate) in a weight ratio of 60:25:15 was added. The solvent was diluted so that the total solid content was 4% by weight, and stirred to prepare a coating liquid for forming a low refractive index layer.

The above-mentioned hard coating forming material is coated on an acrylic film with a lactone ring structure (thickness 40µm, surface smoothness 0.45arcmin) and heated at 90°C for 1 minute, and then the heated coating layer is irradiated with a high-pressure mercury lamp to accumulate light. Ultraviolet light of 300 mJ/cm ² hardens the coating layer, and an acrylic film with a hard coat layer of 4 µm thickness is produced (thickness 44 µm, surface smoothness on the hard coat side 0.4 arcmin). Next, the coating liquid for forming a high refractive index layer is applied on the hard coat layer with a wire bar, and the applied coating liquid is heated at 80° C. for 1 minute to dry, thereby forming a coating film. Use a high-pressure mercury lamp to irradiate the dried coating film with ultraviolet light with a cumulative light intensity of 300mJ/ ^cm2 to harden the coating film and form a high refractive index layer with a thickness of 140nm. Next, the coating liquid for forming the low refractive index layer is applied on the high refractive index layer with a wire bar, and the applied coating liquid is heated at 80° C. for 1 minute to dry, thereby forming a coating film. Use a high-pressure mercury lamp to irradiate the dried coating film with ultraviolet light with a cumulative light intensity of 300mJ/cm ² to harden the coating film and form a low refractive index layer with a thickness of 105nm. In the above manner, a laminated film with a thickness of 44µm and a surface smoothness of 0.4arcmin was obtained.

[Comparative example 1] Except that the high refractive index layer was not formed and the following coating liquid B was used as the coating liquid for forming the low refractive index layer, a low refractive index layer with a thickness of 100 nm was formed in the same manner as in Example 1 to obtain a thickness of 44 µm. It is a laminated film with a surface smoothness of 0.4arcmin.

(Preparation of coating liquid B for forming low refractive index layer) Mix 100 parts by weight of polyfunctional acrylate containing neopentyl erythritol triacrylate as the main component (manufactured by Osaka Organic Chemical Industry Co., Ltd., trade name "Viscoat #300", solid content 100% by weight), and hollow nanosilica 100 parts by weight of particles (manufactured by Nippon Chemical Industry Co., Ltd., trade name "THRULYA 5320", solid content 20% by weight, weight average particle diameter 75 nm), fluorine-containing additive (manufactured by Shin-Etsu Chemical Industry Co., Ltd., trade name "KY- 1203", solid content 20% by weight) 12 parts by weight and photopolymerization initiator (manufactured by BASF, trade name "OMNIRAD907", solid content 100% by weight) 3 parts by weight. To this mixture, a mixed solvent of TBA (tertiary butanol), MIBK (methyl isobutyl ketone) and PMA (propylene glycol monomethyl ether acetate) in a weight ratio of 60:25:15 was added. The solvent was diluted so that the total solid content was 4% by weight, and stirred to prepare a coating liquid B for forming an antireflection and low refractive layer.

[Comparative example 2] Except that the high refractive index layer and the low refractive index layer were not formed, a laminated film with a thickness of 44 μm and a surface smoothness of 0.4 arcmin was obtained in the same manner as in Example 1.

＜Evaluation＞ (1)30° normal reflectivity A test piece with a size of 50 mm × 50 mm was cut out from the laminated film of Example 1, Comparative Example 1, and Comparative Example 2, and attached to a black acrylic plate using an adhesive to obtain a measurement sample. A spectrophotometer (manufactured by Hitachi High-Tech Co., trade name "U-4100") was used as a measuring device to measure the normal reflectance spectrum. The measurement wavelength is set to the range of 420nm to 680nm, and the incident angle of light to the measurement sample is set to 30°.

The 30° normal reflectance spectra of the laminated films of Example 1, Comparative Example 1 and Comparative Example 2 are shown in Figure 5. As shown in Figure 5, the maximum value of the 30° normal reflectance spectrum of the laminated film of Example 1 in the wavelength range of 420 nm to 680 nm is 0.85%. In addition, the normal reflectance at 30° at a wavelength of 450nm is 0.15%, and the normal reflectance at 30° at a wavelength of 600nm is 0.13%. In addition, the results of Comparative Example 1 and Comparative Example 2 are as follows.

[Table 1]

(2) Appearance 1 The laminated films of Example 1, Comparative Example 1 and Comparative Example 2 were attached to a black acrylic plate using an adhesive to obtain a measurement plate. In a dark room, a surface light-emitting unit (LED light box "LLBK1" manufactured by AItec) was installed at a position 18 cm away from the measurement plate so as to face the measurement plate, and the surface light-emitting unit used the dimmer 1 to irradiate light toward the measurement plate. , confirm the appearance of the measurement plate with the naked eye (reflective visual appearance). The reflective visual appearance is shown in Figure 6(a), Figure 6(b) and Figure 6(c). Specifically, Figure 6(a) shows the results when the white display light is irradiated, Figure 6(b) shows the results when the blue light (wavelength 450nm±30nm) is irradiated, and Figure 6(c) shows the results when the red light is irradiated. (wavelength 630nm±30nm).

(3) Appearance 2 The laminated films of Example 1, Comparative Example 1 and Comparative Example 2 were attached to a transparent glass plate using an adhesive to obtain a measurement plate. A surface light-emitting unit (LED light box "LLBK1" manufactured by AItec Corporation) was installed in a dark room and a measurement plate was placed on its light-emitting surface. In this state, the measurement plate when light was irradiated from the surface light-emitting unit with the dimmer 1 was visually confirmed. appearance (transmissive visual appearance). The transmission visual appearance is shown in Figure 7(a), Figure 7(b), Figure 7(c) and Figure 7(d). Figure 7(a) shows the results when the white display light is irradiated, Figure 7(b) shows the results when the blue light (wavelength 450nm±30nm) is irradiated, and Figure 7(c) shows the results when the red light (wavelength 630nm±30nm) is irradiated. 30nm), Figure 7(d) shows the results when green light (wavelength 530nm±30nm) is irradiated.

As shown in Figure 6(a), Figure 6(b) and Figure 6(c), compared with Comparative Example 1 and Comparative Example 2, the reflective visual appearance of Example 1 is particularly excellent. In the above evaluation, it is assumed that a black acrylic plate is used in combination with an absorptive polarizing member. However, the difference in reflective visual appearance can also be confirmed using a transparent glass plate. According to Embodiment 1, we believe that the problem of ghost images that may occur due to reflected light can be very well solved in the display system according to the embodiment of the present invention. In addition, as shown in Figures 7(a), 7(b), 7(c) and 7(d), the transmission visual appearance of Example 1, Comparative Example 1 and Comparative Example 2 does not change significantly.

The present invention is not limited to the above-described embodiment, and various modifications are possible. For example, it may be replaced by a structure that is substantially the same as that shown in the above-mentioned embodiment, a structure that can produce the same effects, or a structure that can achieve the same purpose.

industrial availability The lens part according to the embodiment of the present invention can be used in a display body such as VR goggles, for example.

2:Display system 4: Lens department 12:Display components 12a:Display surface 14: Reflective polarizing component 14a:Multi-layer structure 16: First lens part 18: Half mirror 20: First phase difference member 22: Second phase difference member 22a: 2ndλ/4 member 22b: Positive C board 24: Second lens unit 26:User's Eyes 28:Absorptive polarizing component 30: The third phase difference component 31: First protective component 32: Second protective component 34:Laminated film 36:Substrate 38: Surface treatment layer 38a:hard coating 38b:Functional layer 41: Next layer 42: Next layer 43: Next layer 44: Next layer 45: Next layer 46: Next layer 100: The first layering part 200:Second laminated part A,B:layer X,Y,Z: axis

FIG. 1 is a schematic diagram showing the schematic structure of a display system according to an embodiment of the present invention. FIG. 2 is a schematic cross-sectional view showing an example of details of the lens portion of the display system shown in FIG. 1 . FIG. 3 is a schematic cross-sectional view showing the schematic structure of a laminated film according to an embodiment of the present invention. FIG. 4 is a schematic perspective view showing an example of a multi-layer structure included in a reflective polarizing film. FIG. 5 is a graph showing the 30° normal reflectance spectrum of the laminated films of Example 1, Comparative Example 1 and Comparative Example 2. In Figure 6, (a), (b) and (c) are photos showing the results of appearance evaluation. In Figure 7, (a), (b), (c) and (d) are photos showing the results of appearance evaluation.

2:Display system

4: Lens department

12:Display components

12a:Display surface

14: Reflective polarizing component

16: First lens part

18: Half mirror

20: First phase difference member

22: Second phase difference member

24: Second lens unit

26:User's Eyes

Claims (10)

A lens unit used in a display system for displaying images to a user, which has: The reflective polarizing member reflects the light emitted forward from the display surface of the display element that displays the image and passes through the polarizing member and the 1st λ/4 member; The first lens part is arranged on the optical path between the display element and the reflective polarizing member; A half-reflecting mirror is disposed between the display element and the first lens portion. The half-reflecting mirror transmits the light emitted from the display element and directs the light reflected by the reflective polarizing member toward the reflective polarizer. Component reflection; The second lens part is arranged in front of the aforementioned reflective polarizing member; The 2λ/4 member is arranged on the optical path between the half-mirror and the reflective polarizing member; and The first protective member and the second protective member are arranged on the optical path between the aforementioned half mirror and the aforementioned reflective polarizing member; The aforementioned first protective member and the aforementioned second protective member are arranged to face each other across a space; and The maximum value of the 30° normal reflectance spectrum of each of the first protective member and the second protective member in the wavelength range of 420 nm to 680 nm is 1.4% or less. The lens part of claim 1, wherein the 30° normal reflectance of each of the first protective member and the second protective member at a wavelength of 450 nm is 0.5% or less. The lens part of Claim 1, wherein the 30° normal reflectance of each of the first protective member and the second protective member at a wavelength of 600 nm is 0.5% or less. The lens part of claim 1, wherein the surface smoothness of each of the first protective member and the second protective member is 0.5 arcmin or less. The lens part of Claim 1, wherein the 2nd λ/4 member satisfies Re(450)<Re(550). The lens part of claim 1 has: The first laminate part includes the aforementioned 2λ/4 member and the aforementioned first protective member; and The second laminate part includes the aforementioned reflective polarizing member and the aforementioned second protective member. The lens part of claim 6, wherein the second laminate part includes an absorptive polarizing member disposed between the reflective polarizing member and the second lens part. The lens part of claim 6, wherein the second laminate part includes a 3λ/4 member disposed between the reflective polarizing member and the second lens part. The lens part of Claim 8, wherein the 3rd λ/4 member satisfies Re(450)<Re(550). A laminated film used in a display method with the following procedures: The process of causing the light emitted by the polarizing member and the first λ/4 member to display the image to pass through the half mirror and the first lens part; The process of causing the light passing through the half-reflecting mirror and the first lens part to pass through the 2λ/4 member; The process of reflecting the light passing through the 2λ/4 member toward the half-mirror through the reflective polarizing member; The process of allowing the light reflected by the reflective polarizing member and the half-reflecting mirror to transmit through the reflective polarizing member through the 2λ/4 member; and The process of causing the light transmitted through the reflective polarizing member to pass through the second lens part; The laminated film is disposed on the optical path between the half mirror and the reflective polarizing member and is in contact with the space formed between the first lens part and the second lens part; and, The maximum value of the 30° normal reflectance spectrum of the aforementioned laminated film in the wavelength range of 420 nm to 680 nm is 1.4% or less.

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