TW202336469A - Optical laminate, lens part and display method capable of reducing the weight of VR goggles and improving visibility - Google Patents

Abstract

Provided is an optical laminate capable of reducing a weight of VR goggles and improving a visibility. An optical laminate according to an embodiment of the present invention comprises: a laminate film having a base material and a surface treated layer; and a retardation member. The base material of the laminate film is adjacent to the retardation member. The base material of the laminate film includes a (meth)acrylic resin, and the laminate smoothness of the optical laminate is 1.0 arcmin or less.

Description

Optical laminate, lens unit, and display method

The present invention relates to an optical laminated body, a lens unit, and a display method.

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. VR goggles are being considered for use in various situations, so they are expected to 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. 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 an optical laminate that can reduce the weight of VR goggles and improve visibility.

means to solve problems 1. An optical laminated body according to an embodiment of the present invention, comprising: a laminated film having a base material and a surface treatment layer; and a retardation member; in the laminated film, the base material and the retardation member are arranged adjacent to each other; The laminated film and the base material include (meth)acrylic resin; and the laminated body smoothness of the optical laminated body is 1.0 arcmin or less. 2. In the optical laminated body as described in 1 above, the surface smoothness of the base material of the laminated film may be 0.7 arcmin or less. 3. In the optical laminate according to 1 or 2 above, the surface smoothness of the laminated film may be 0.5 arcmin or less. 4. The optical laminated body according to any one of 1 to 3 above, the smoothness of the laminated body may be 0.7 arcmin or less. 5. In the optical laminated body according to any one of 1 to 4 above, the surface treatment layer of the laminated film may also have an anti-reflective function. 6. In the optical laminate according to any one of 1 to 5 above, the retardation member may also include a first retardation layer that exhibits refractive index characteristics of nx>ny≧nz and satisfies Re The relationship of (450)＜Re(550)＜Re(650). 7. In the optical laminate according to any one of 1 to 6 above, the retardation member may include a second retardation layer exhibiting refractive index characteristics of nz>nx≧ny. 8. In the optical laminated body according to any one of 1 to 7 above, the transmittance of the base material of the laminated film at a wavelength of 400 nm may be 20% or less. 9. The optical laminate according to any one of 1 to 8 above may have Re (550) of 130 nm to 160 nm. 10. The lens unit according to the embodiment of the present invention is used in a display system that displays an image to a user, and includes 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. and the light of the 1st λ/4 member; the first lens portion 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 portion. The half-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; and if The optical laminate according to any one of the above items 1 to 9 is arranged on the optical path between the half mirror and the reflective polarizing member. 11. The display method according to the embodiment of the present invention has the following steps: passing the light emitted to display the image through the polarizing member and the first λ/4 member through the half-reflecting mirror and the first lens unit; passing the light passing through the half-reflecting mirror and the step of passing the light of the first lens part through the optical laminate in any one of the above 1 to 9; the step of causing the light passing through the optical laminate to be reflected toward the half-mirror by the reflective polarizing member; by the above-mentioned The optical laminate can include the steps of transmitting the light reflected by the reflective polarizing member and the half-mirror through the reflective polarizing member; and the step of passing the light transmitted through the reflective polarizing member through the second lens portion.

Invention effect According to the optical laminate according to the embodiment of the present invention, VR goggles can be lightweight and have improved 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 .

There may be components arranged in front from the half mirror or the first lens unit (in the example of the figure, the half mirror 18, the first lens unit 16, the second phase difference member 22, the reflective polarizer The member 14 and the second lens portion 24) are collectively referred to as the lens portion (lens portion 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 2 λ/4 member that 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 Convert to 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 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 a 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. The 1st λ/4 member should satisfy the relationship of Re(450)＜Re(550)＜Re(650). 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. The 2λ/4 member should satisfy the relationship of Re(450)＜Re(550)＜Re(650). 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, the member disposed between the first lens part 16 and the second lens part 24 is preferably provided on either the first lens part 16 or the second lens part 24 through an adhesive layer to be integrated. According to this aspect, for example, each member can be excellent in performance. The subsequent layer can be formed with 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 part 4 includes a first lens part 16, a first laminate part 100 provided adjacent to the first lens part 16, a second lens part 24, and a second laminate part provided adjacent to the second lens part 24. Department 200. In the example shown in FIG. 2 , the first lamination unit 100 and the second lamination unit 200 are arranged with a gap therebetween. Although not shown in the figure, the half mirror may be integrally provided on the first lens part 16 . Hereinafter, the first laminated part may be called an optical laminated body.

The first laminate part 100 includes the second retardation member 22 and an adhesive layer (for example, an adhesive layer) disposed between the first lens part 16 and the second retardation member 22 , and is disposed on the first through the adhesive layer 41 The 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 protection member 31 is laminated on the second phase difference member 22 through an adhesive layer (eg, adhesive layer) 42 and is disposed adjacent to the second phase difference member 22 . The first protective member 31 may be located on the outermost surface of the first laminate part 100 . In addition, in this specification, the term "adjacent" means not only being directly adjacent but also including being adjacent via an adhesive layer.

In the example shown in FIG. 2 , the second retardation member 22 includes, in addition to the 2λ/4 member (first retardation layer) 22 a , a member (the first retardation layer) having a refractive index characteristic showing the relationship nz>nx≧ny. Two phase difference layers) 22b. The second phase difference member 22 has a laminated structure of a first phase difference layer 22a and a second phase difference layer 22b. By using the member 22b showing the relationship nz>nx≧ny, light leakage (for example, oblique light leakage) can be prevented. As shown in FIG. 2 , among the second phase difference members 22 , the 2nd λ/4 member 22 a is preferably located forward of the member 22 b showing the relationship nz>nx≧ny.

It is preferable that the 2λ/4 member (first retardation layer) 22a and the member (second retardation layer) 22b showing the relationship nz>nx≧ny are laminated through an adhesive layer (not shown). The second retardation member 22 includes a first retardation layer 22a, an adhesive layer, and a second retardation layer 22b. By laminating the retardation layer using an adhesive layer, the occurrence of cracks or cracks in the retardation layer can be suppressed. And can prevent the phase difference layer from peeling off. Furthermore, an optical laminate with excellent durability can be obtained.

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 dimethanol, The structural unit of at least one dihydroxy compound in the group consisting of di, tri or polyethylene glycol, and alkylene glycol or spiroglycerol. The polycarbonate resin preferably contains structural units derived from fluorine-based dihydroxy compounds, structural units derived from isosorbide-based dihydroxy compounds, structural units derived from alicyclic dimethanol, and/or derived from di- or tri-hydroxy compounds. Or structural units of polyethylene glycol; more preferably, they include structural units derived from fluorine dihydroxy compounds, structural units derived from isosorbide dihydroxy compounds, and structural units derived from di, tri or polyethylene 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 retardation Rth (550) in the thickness direction of the member (second retardation layer) whose refractive index characteristics exhibit the relationship nz>nx≧ny is preferably -260nm~-10nm, more preferably -230nm~-15nm, and more preferably It is -215nm~-20nm. In one embodiment, the refractive index of the second retardation layer exhibits the relationship nx=ny, which is a so-called positive C plate. 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. For example, it also includes the case where Re(550) is less than 10 nm. In another embodiment, the refractive index of the second phase difference layer exhibits the relationship nx>ny. At this time, the in-plane phase difference Re(550) of the second retardation layer is preferably 10 nm to 150 nm, more preferably 10 nm to 80 nm.

The member whose refractive index characteristics exhibit the relationship nz>nx≧ny can be formed of any appropriate material. It is preferable to consist of a thin film containing liquid crystal material fixed in a homeotropic 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 liquid crystal compound and the method for forming the thin film include the liquid crystal compound and the method for forming the liquid crystal compound and the method described in paragraphs [0020] to [0042] of Japanese Patent Application Laid-Open No. 2002-333642. At this time, the thickness should be 0.1µm~5µm, more preferably 0.5µm~4µm.

As another ideal specific example, the member whose refractive index characteristics exhibit the relationship nz>nx≧ny may be a retardation film formed of the fumarate diester resin described in Japanese Patent Application Laid-Open No. 2012-32784. At this time, the thickness should be 5µm~50µm, more preferably 10µm~35µm.

The adhesive layer contained in the second phase difference member 22 can be formed of any appropriate adhesive. In the process of forming the adhesive layer, the state of the adhesive changes irreversibly from a liquid to a solid. It has the property of being fluid during coating and hardening by hardening treatment (such as active energy ray irradiation, heating). It is preferable to use a hardening adhesive as the adhesive. Specifically, the adhesive layer is preferably a hardened layer of resin. As for the hardening adhesive, it is preferable to use ultraviolet hardening adhesive.

The ultraviolet curing adhesive contains curable monomers such as compounds having (meth)acrylyl groups and compounds having vinyl groups as curable monomers. Preferably, compounds having a (meth)acrylyl group can be used. Here, (meth)acrylyl group means an acrylyl group and/or a methacrylyl group.

The thickness of the adhesive layer included in the phase difference member is, for example, 0.5 µm or more and 3 µm or less, preferably 2 µm or less, more preferably 1.3 µm or less, more preferably 1.1 µm or less, especially 0.9 µm or less. With this thickness, an optical laminate having extremely excellent smoothness can be obtained.

The above-mentioned first protective member typically includes a base material. The thickness of the substrate should be 5µm~80µm, more preferably 10µm~50µm, more preferably 15µm~40µm. The surface smoothness of the base material is preferably 0.7 arcmin or less, more preferably 0.6 arcmin or less, more preferably 0.5 arcmin or less, especially 0.45 arcmin or less. In the above display system, the image will be amplified by the lens part (for example, through a convex lens), so the smoothness of the optical laminate may significantly affect the visibility. Since the base material of the protective member that may be located on the outermost surface of the laminate portion has excellent smoothness, the optical laminate obtained by using it can also have extremely excellent smoothness. Furthermore, according to the optical laminate, remarkably excellent visibility can be achieved in the above display system. For example, clear images without distortion can be achieved. The surface smoothness of the base material is, for example, 0.1 arcmin or more. In addition, surface smoothness can be measured by focusing illumination light on the surface of the object.

The base material can be composed of any suitable film. Examples of materials that constitute the main component of the film constituting the base material include cellulose-based resins such as triacetylcellulose (TAC), polyester-based, polyvinyl alcohol-based, polycarbonate-based, polyamide-based, and polyamide-based resins. Resins such as imine series, polyether series, polystyrene series, polystyrene series, polynorphenyl series, cyclic olefin series, polyolefin series, (meth)acrylic series and acetate series. Here, (meth)acrylic acid means acrylic acid and/or methacrylic acid. In one embodiment, the base material is preferably composed of (meth)acrylic resin. By using (meth)acrylic resin, a base material having excellent smoothness (for example, satisfying the above-mentioned surface smoothness) can be formed into a film by extrusion molding. Furthermore, a protective member excellent in smoothness can be obtained.

For example, the transmittance of the base material at a wavelength of 400 nm may be 20% or less.

The first protective member is preferably composed of a laminated film having a base material and a surface treatment layer formed on the base material. The thickness of the laminated film is preferably 10µm~80µm, more preferably 15µm~60µm, and more preferably 20µm~45µm. The thickness of the surface treatment layer should be 0.5µm~10µm, more preferably 1µm~7µm, more preferably 2µm~5µm.

The surface treatment layer represents a hard coat layer. The hard coat layer is typically formed by applying a hard coat forming material to a base material 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 should be 0.5µm~10µm, more preferably 1µm~7µm, more preferably 2µm~5µm.

The surface treatment layer should include a functional layer. The functional layer should function as an anti-reflective layer. In a preferred embodiment, the surface treatment layer includes the hard coat layer and the anti-reflective layer in order from the base material side. The thickness of the functional layer is preferably 0.05µm~10µm, more preferably 0.1µm~5µm, and more preferably 0.1µm~2µm.

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 surface treatment layer can have any appropriate function. The surface treatment layer preferably has an anti-reflection function from the viewpoint of suppressing light loss at the interface with air and improving visibility. In one embodiment, the maximum value of the 5° normal reflectance spectrum of the first protective member in the wavelength range of 420 nm to 680 nm is preferably 2.0% or less, more preferably 1.2% or less, more preferably 1.0% or less, especially is less than 0.8%. Here, the 5° normal reflectance can be measured, for example, by attaching the measurement object to a black acrylic plate using an adhesive to prepare a measurement sample. The measurement device uses a spectrophotometer (Hitachi High-Tech Co., Ltd. (manufactured by U-4100 under the trade name "U-4100"), and the incident angle of light to the measurement sample was set to 5°.

The surface smoothness of the first protective member is preferably 0.5 arcmin or less, more preferably 0.4 arcmin or less. In essence, the surface smoothness of the first protective member is, for example, 0.1 arcmin or more. The laminated body smoothness of the optical laminated body 100 is 1.0 arcmin or less, preferably 0.9 arcmin or less, more preferably 0.8 arcmin or less, more preferably 0.7 arcmin or less. By satisfying the smoothness of the laminated body, the optical laminated body can suppress the occurrence of diffuse light and suppress the image from becoming unclear. The laminated body smoothness of the optical laminated body 100 is, for example, 0.1 arcmin or more. In addition, the smoothness of the laminated body can be obtained by irradiating the object with irradiation light and detecting the reflection and transmission of each member constituting the object (laminated body).

The optical laminated body 100 can have high transmittance. For example, the Y value of the visual sensitivity correction unit transmittance of the optical laminate 100 is, for example, 90% or more, preferably 93% or more, more preferably 94% or more, and more preferably 95% or more. The transmittance can be, for example, the single-piece transmittance Ts measured using an ultraviolet-visible light spectrophotometer (V-7100, manufactured by JASCO Corporation). Here, Ts is the Y value measured using the 2-degree field of view (C light source) of JIS Z 8701 and corrected for visual sensitivity.

The in-plane phase difference Re(550) of the optical layered body 100 may be, for example, 100 nm to 190 nm, 110 nm to 180 nm, 130 nm to 160 nm, or 135 nm to 155 nm.

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 with a space therebetween. Like the first protective member, the second protective member can be typically 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 reflection characteristics, effects, smoothness, 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. 3 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; layer A and The refractive index difference of layer B is large in the x-axis direction, but 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 extend and dye the laminated body to make the PVA-based resin layer into an absorption-type polarized light membrane. 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.

The thickness of the adhesive layer used for laminating each of the above-mentioned components can be set to any appropriate thickness. The thickness of the adhesive layer used in the lamination of each of the above components is preferably 3 µm or more and 20 µm or less, and may be 15 µm or less, 10 µm or less, or 7 µm or less. According to this thickness, the degree of unevenness on the surface of the adhesive layer can be suppressed, and the smoothness of the laminate portion can be excellent.

The adhesive layer can be composed of any suitable adhesive. Specific examples include acrylic adhesives, rubber adhesives, silicone adhesives, polyester adhesives, urethane adhesives, epoxy adhesives, and polyether adhesives. By adjusting the type, quantity, combination and blending ratio of the monomers that form the base resin of the adhesive, as well as the blending amount of the cross-linking agent, reaction temperature, reaction time, etc., it is possible to prepare a product with the desired characteristics that meets the purpose. Adhesive. The base resin of the adhesive can be used alone or in combination of two or more. It is preferable to use acrylic resin as the base resin. Specifically, the adhesive layer is preferably composed of an acrylic adhesive.

For example, the adhesive layer can be formed by applying an adhesive composition including a base resin, additives such as a cross-linking agent, and a solvent, and drying the adhesive composition. The adhesive composition can be directly applied to the adherend, or it can also be applied to a separately prepared base material film or other substrate. Drying is typically performed by heating.

For example, by adjusting the film thickness of the coating film of the adhesive composition, an adhesive layer excellent in smoothness can be obtained. If the film thickness is too thick, heating will cause the liquid to flow due to the temperature difference in the coating film, and an adhesive layer with a large surface unevenness will be formed.

Furthermore, for example, by controlling the drying conditions of the coating film of the adhesive composition, an adhesive layer with excellent smoothness can be obtained. Specifically, by adjusting the air volume and wind speed blown to the coating film during drying, an adhesive layer with excellent smoothness can be obtained. If the air volume and wind speed blown to the coating film are too large, waves will be generated on the coating film and an adhesive layer with a large surface unevenness will be formed. In one embodiment, it is advisable to dry the coating film in a temperature environment of 65°C to 110°C with the wind speed adjusted to a range of 2m/min to 15m/min, preferably to 2m/min to 8m/min. Dry after minutes. For example, it is suitable to adjust the temperature and wind speed to the above-mentioned temperature and wind speed near the entrance of a drying oven after coating. Specifically, the temperature and wind speed can be adjusted from the oven inlet to the center of the oven.

Example Hereinafter, the present invention will be specifically described through examples, but the present invention is not limited by these examples. In addition, the thickness, phase difference value 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"). ＜Phase difference＞ The phase difference value at each wavelength was measured at 23°C using a Mueller matrix polarimeter (manufactured by Axometrics, product name "Axoscan"). ＜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□. When the measurement object is an adhesive layer, the adhesive layer is attached to a slide glass (manufactured by Matsunami Glass Industry Co., Ltd., product name "S200200"), and the smoothness of the exposed adhesive surface is measured. When the measurement object is a film, an acrylic adhesive layer with a thickness of 5 µm and less unevenness is formed on the above-mentioned glass, and the film to be measured is laminated on the adhesive surface in a manner that prevents foreign matter, air bubbles, and deformation streaks from entering. The smoothness of the surface opposite to the adhesive layer is measured. In addition, the surface smoothness of the acrylic adhesive layer with a thickness of 5 µm and few unevenness is 0.30 arcmin. 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 λ/4 member) Polymerization was performed using a batch polymerization apparatus consisting of two vertical reactors equipped with stirring blades and a reflux cooler controlled to 100°C. Feed in 29.60 parts by mass (0.046 mol) of bis[9-(2-phenoxycarbonylethyl)fluoren-9-yl]methane, 29.21 parts by mass (0.200 mol) of isosorbide (ISB), and spiroglycerol (SPG) 42.28 parts by mass (0.139 mol), 63.77 parts by mass (0.298 mol) of diphenyl carbonate (DPC) and 1.19×10 ^-2 parts by mass (6.78×10 ^-5 mol) of calcium acetate monohydrate as a catalyst. After the reactor was replaced with nitrogen under reduced pressure, it was heated with a heat medium, and stirring was started when the internal temperature reached 100°C. The internal temperature was brought to 220°C 40 minutes after the start of the temperature rise, and the pressure was reduced while maintaining the temperature. After reaching 220°C, it was adjusted to 13.3 kPa in 90 minutes. The phenol vapor generated by the polymerization reaction is introduced into the reflux cooler at 100°C, so that a small amount of monomer components contained in the phenol vapor is returned to the reactor, and the uncondensed phenol vapor is introduced into the condensator at 45°C for recovery. After introducing nitrogen into the first reactor and temporarily returning it to atmospheric pressure, the oligomerized reaction liquid in the first reactor is moved to the second reactor. Next, the temperature increase and pressure reduction in the second reactor were started, and the internal temperature was adjusted to 240° C. and the pressure to 0.2 kPa over 50 minutes. Then, polymerization is performed until a predetermined stirring power is reached. At the time point when the predetermined power is reached, nitrogen is introduced into the reactor to restore the pressure, the generated polyester carbonate resin is extruded into water, and the bundles are cut to obtain pellets.

The obtained polyester carbonate resin (pellets) was vacuum-dried at 80°C for 5 hours, and then used a single-screw extruder (manufactured by Toshiba Machine Co., Ltd., cylinder set temperature: 250°C) and a T-die (width 200mm). , set temperature: 250℃), cooling roller (set temperature: 120~130℃) and film forming device of the winding machine to produce a long resin film with a thickness of 135μm. The obtained long resin film was stretched in the width direction at a stretching temperature of 143°C and a stretching ratio of 2.8 times to obtain a stretched film with a thickness of 47 μm. The Re(550) of the obtained stretched film was 143 nm, the Re(450)/Re(550) was 0.86, and the Nz coefficient was 1.12.

(Formation of positive C plate) The side chain represented by the following chemical formula (1) (numbers 65 and 35 in the formula represent mol% of monomer units, expediently expressed as a block polymer: weight average molecular weight 5000) 20 parts by weight of a liquid crystal polymer, 80 parts by weight of a polymerizable liquid crystal exhibiting a nematic liquid crystal phase (manufactured by BASF: trade name PaliocolorLC242), and 5 parts by weight of a photopolymerization initiator (manufactured by Ciba Specialty Chemicals: trade name IRGACURE 907) It was dissolved in 200 parts by weight of cyclopentanone to prepare a liquid crystal coating liquid. Next, the coating liquid was applied to the vertically oriented PET substrate using a bar coater, and then heated and dried at 80° C. for 4 minutes to orient the liquid crystal. The liquid crystal layer was irradiated with ultraviolet rays to harden the liquid crystal layer, thereby forming a positive C plate with a thickness of 4 μm and an Rth (550) of -100 nm on the base material. [Chemical formula 1]

(Preparation of protective member) The following hard coat forming material is applied to an acrylic film with a lactone ring structure (thickness 40µm, surface smoothness 0.45arcmin) and heated at 90°C for 1 minute, and then heated with a high-pressure mercury lamp The coating layer was irradiated with ultraviolet rays with a cumulative light intensity of 300 mJ/cm ² to harden the coating layer, and an acrylic film with a hard coat layer of 4 µm thickness was produced (thickness 44 µm, surface smoothness on the hard coat side 0.4 arcmin). Next, the following coating liquid A for forming an antireflection layer was applied on the above-mentioned hard coat layer with a wire bar, and the applied coating liquid was 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 an anti-reflective layer A with a thickness of 140nm. Next, the following anti-reflective layer forming coating liquid B is applied on the anti-reflective layer A 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 an anti-reflective layer B with a thickness of 105nm. A protective member (thickness 44µm, surface smoothness on the antireflection layer side 0.4arcmin) was obtained in the above manner.

(hard coat forming material) 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.

(Coating liquid A for antireflection 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 diluting solvent so that the solid content became 12% by weight, and the mixture was stirred to prepare a coating liquid A for forming an antireflection layer.

(Coating liquid B for antireflection layer formation) 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 parts 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 B for forming an antireflection layer.

(Formation of adhesive layer) A monomer mixture containing 94.9 parts by weight of butyl acrylate, 5 parts by weight of acrylic acid, and 0.1 part by weight of 2-hydroxyethyl acrylate was fed into a four-necked flask equipped with a stirring blade, a thermometer, a nitrogen gas inlet pipe and a cooler. And with respect to 100 parts by weight of this monomer mixture, 0.3 parts by weight of benzyl peroxide as a polymerization initiator was fed together with ethyl acetate, and nitrogen was introduced while stirring slowly to replace the nitrogen in the flask. , maintaining the liquid temperature in the flask at 60°C for 7 hours of polymerization reaction. Next, ethyl acetate was added to the obtained reaction liquid to adjust the solid content concentration to 30% by weight, thereby preparing an acrylic polymer solution with a weight average molecular weight (Mw) of 2.2 million. Per 100 parts by weight of the solid content of the obtained acrylic polymer solution, 0.6 parts by weight of trimethylolpropane/toluene diisocyanate adduct (trade name: Coronate L, manufactured by Tosoh Corporation) and 0.075 part by weight of silane coupling agent (trade name: KBM403, manufactured by Shin-Etsu Chemical Industry Co., Ltd.) to prepare an acrylic adhesive. The obtained acrylic adhesive composition was applied to the base film and dried to form an adhesive layer with a thickness of 12 µm and an adhesive layer with a thickness of 15 µm. Surface smoothness is 0.25arcmin.

(Production of optical laminates) The above-mentioned positive C plate is bonded to the above-mentioned λ/4 member (stretched film) through an ultraviolet curable adhesive (thickness after curing: 1 µm) to obtain a phase difference member. On the λ/4 member side of the obtained retardation member, the above-mentioned protective member (acrylic film formed with a hard coat layer and an anti-reflective layer) is bonded through the above-mentioned adhesive layer (thickness: 12 μm). Here, the acrylic film of the protective member is attached so that it is located on the λ/4 member side. Next, the above-mentioned adhesive layer (thickness: 15 μm) was bonded to the positive C plate side of the retardation member to obtain an optical laminated body.

[Example 2] An optical laminated body was obtained in the same manner as in Example 1, except that the formation conditions of the adhesive layer were changed to form an adhesive layer with a surface smoothness of 0.4 arcmin.

[Comparative example 1] When making protective components, use TAC film (thickness 60µm, surface smoothness 0.5arcmin) to replace the acrylic film with lactone ring structure, and set the thickness of the hard coating to 12µm to obtain a thickness of 72µm and an anti-reflective layer side An optical laminated body was obtained in the same manner as in Example 2 except that the surface smoothness of the protective member was 0.5 arcmin.

The following evaluation was performed on the optical laminates obtained in Examples and Comparative Examples. The evaluation results are shown in Table 1. (1)Laminated body smoothness The smoothness of the laminated body was measured using a phase shift laser interferometer (manufactured by Zygo, product name: "DynaFiz"). Specifically, the optical laminate is laminated on a slide glass (manufactured by Matsunami Glass Industry Co., Ltd., product name "S200200") in a manner that prevents foreign matter, air bubbles, and deformed streaks from entering. Next, in order to remove the influence of microbubbles, degassing was performed using a pressure degassing device (autoclave). The degassing conditions were set to 50°C, 0.5MPa, and 30 minutes. After defoaming, the sample was naturally cooled at room temperature for 30 minutes or more to obtain a measurement sample. The measurement sample is placed on a measurement table with an anti-vibration table, and a laser with a single wavelength (wavelength 633nm) is used to interfere with a reference instrument that has ensured flatness, and the relative displacement within a predetermined area (30mmφ circle) is measured. . Regarding the analysis, the value obtained by multiplying the angle index "Slope magnitude RMS" by selecting the value of the frequency from 0.1/mm to 1/mm and multiplying it by 2 times (equivalent to 2σ) is defined as the smoothness of the laminated body ( Unit: arcmin). (2) Reflection An optical lens (manufactured by Thorabs, trade name "LA1145") and a point light source (manufactured by Hamamatsu Photonics, model "L8425-01") were used to evaluate the transmission (lens transmitted light) of the optical laminate. Specifically, optical laminates cut into circular shapes of 45 mmφ are laminated on the flat side of the optical lens in a manner that prevents foreign matter, air bubbles, and deformed streaks from entering the surface. Next, in order to remove the influence of microbubbles, degassing was performed using a pressure degassing device (autoclave). The degassing conditions were set to 50°C, 0.5MPa, and 30 minutes. After defoaming, the sample was naturally cooled at room temperature for 30 minutes or more to obtain a measurement sample. A point light source, an optical lens (measurement sample), and a screen are set up in order, and the light from the point light source that passes through the optical lens is mapped on the screen, and the reflection is evaluated. Here, the lens is held by a holder at a position where light from the point light source is incident from the convex side of the optical lens. The distance from the point light source to the screen is set to 1050mm, and the distance from the optical lens to the screen is set to 130mm. In addition, the transparency is evaluated by 10 evaluators using the naked eye to observe the light reflected on the screen through the optical lens and determine whether there are wrinkles and undulations. The number of evaluators who judged that there were no wrinkles or undulations is shown in Table 1.

[Table 1]

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 optical laminated body according to the embodiment of the present invention can be used for 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: First phase difference layer 22b: Second phase difference layer 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 41: Next layer 42: Next layer 43: Next layer 44: Next layer 45: Next layer 46: Next layer 100: First laminate part (optical laminate) 200:Second Lamination Department A,B:layer

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 perspective view showing an example of a multi-layer structure included in a reflective polarizing film.

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 (11)

An optical laminated body includes: a laminated film having a base material and a surface treatment layer; and a retardation member; The laminated film, the base material and the retardation member are arranged adjacent to each other; The base material of the laminated film contains (meth)acrylic resin; and The laminated body smoothness of this optical laminated body is 1.0 arcmin or less. The optical laminated body according to claim 1, wherein the surface smoothness of the laminated film and the base material is 0.7 arcmin or less. The optical laminated body according to claim 1, wherein the surface smoothness of the laminated film is 0.5 arcmin or less. For example, in the optical laminate of claim 1, the smoothness of the laminate is 0.7 arcmin or less. The optical laminated body according to claim 1, wherein the laminated film and the surface treatment layer have an anti-reflection function. The optical laminated body of claim 1, wherein the retardation member includes a first retardation layer, and the first retardation layer exhibits refractive index characteristics of nx>ny≧nz and satisfies Re(450)<Re(550)< The relationship of Re(650): Here, Re(450) represents the in-plane phase difference measured at 23°C using light with a wavelength of 450 nm, Re(550) represents the in-plane phase difference measured at 23°C using light with a wavelength of 550 nm, and Re(650) represents In-plane phase difference measured with light of wavelength 650nm at 23°C. The optical laminated body according to claim 1, wherein the retardation member includes a second retardation layer exhibiting refractive index characteristics of nz>nx≧ny. The optical laminated body according to claim 1, wherein the transmittance of the laminated film and the base material at a wavelength of 400 nm is 20% or less. In the optical laminated body of claim 1, the in-plane phase difference Re (550) measured with light of a wavelength of 550 nm at 23° C. is 130 nm to 160 nm. A lens unit used in a display system for displaying images to a user, which has: A reflective polarizing member that 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 1λ/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 polarizing member. reflection; The second lens part is arranged in front of the aforementioned reflective polarizing member; and The optical laminate according to any one of claims 1 to 9 is arranged on the optical path between the half mirror and the reflective polarizing member. A display method with the following steps: The step of passing the light displaying the image emitted through the polarizing member and the first λ/4 member through the half mirror and the first lens unit; The step of passing the light passing through the half-reflecting mirror and the first lens part through the optical laminate according to any one of claims 1 to 9; The step of reflecting the light passing through the optical laminate toward the half-mirror on the reflective polarizing member; The step of transmitting the light reflected by the reflective polarizing member and the half-reflecting mirror through the reflective polarizing member through the optical laminate; and The step of passing the light transmitted through the reflective polarizing member through the second lens part.

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