JP2019167113A - Vehicular mirror with image display function - Google Patents

Abstract

To provide a vehicular mirror with an image display function, that is capable of bright image display and that allows observation of a mirror reflected image without irregularities.SOLUTION: Provided is a vehicular mirror with an image display function, that includes a half-mirror and an image display device. The half-mirror includes a high-Re phase difference film and a reflective layer. In the mirror with the image display function, the high-Re phase difference film, the reflective layer, and the image display device are disposed in this order, the high-Re phase difference film has a front face phase difference of 5000 nm or more, and the reflective layer is a linearly polarizing reflective layer or a circularly polarizing reflective layer.SELECTED DRAWING: None

Description

  The present invention relates to a mirror with an image display function for a vehicle.

  For example, Patent Document 1 describes a mirror with a vehicle image display function that can display an image such as an image captured by a vehicle-mounted camera on a vehicle mirror. In the mirror with a vehicle image display function disclosed in Patent Document 1, a liquid crystal display device is provided inside the housing of the vehicle mirror, and an image is displayed through a half mirror provided on the front surface of the vehicle mirror. The image display on the mirror is realized.

JP 2014-2011146 A JP 2011-45427 A

A half mirror has a visible light transmittance of usually about 30% to 70%, and a configuration in which a half mirror is provided has a potential problem that an image becomes darker than an image having no half mirror. .
On the other hand, Patent Document 2 discloses a mirror with an information display function applied to interior, cosmetic, crime prevention, and safety mirrors. Here, it is described that it is possible to eliminate light loss by using a reflective polarizing plate as a half mirror. However, when the present inventors configured a mirror with an image display function using a reflective polarizing plate and used it in a vehicle, unevenness in light and darkness and color unevenness (rainbow color, etc.) occurred in the mirror reflection image.
An object of the present invention is to provide a mirror with an image display function for a vehicle that can display a bright image and can observe a mirror reflection image without unevenness.

  The present inventors diligently studied to solve the above problems, and found that the above-described unevenness of the mirror reflection image can be confirmed when an external scenery through the rear glass of the vehicle is observed. The present invention was completed by repeating the above.

That is, the present invention provides the following [1] to [11].
[1] A mirror with an image display function for a vehicle,
Including half mirror and image display device,
The half mirror includes a high Re retardation film and a reflective layer,
In the mirror with an image display function, the high Re retardation film, the reflective layer, and the image display device are arranged in this order,
The high Re retardation film has a front phase difference of 5000 nm or more,
The mirror with an image display function, wherein the reflective layer is a linearly polarized light reflective layer or a circularly polarized light reflective layer.
[2] The mirror with an image display function according to [1], wherein the front phase difference is 7000 nm or more.
[3] The mirror with an image display function according to [1] or [2], wherein the reflective layer is a circularly polarized reflective layer.
[4] The mirror with an image display function according to [3], wherein the circularly polarized light reflection layer includes a cholesteric liquid crystal layer.
[5] The mirror with an image display function according to [4], wherein the circularly polarized light reflection layer includes three or more cholesteric liquid crystal layers.

[6] including a quarter-wave plate,
The mirror with an image display function according to [4] or [5], wherein the half mirror includes the high Re retardation film, the circularly polarizing reflection layer, and the quarter wavelength plate in this order.
[7] The mirror with an image display function according to [6], wherein the circularly polarizing reflection layer and the quarter-wave plate are in direct contact with each other.
[8] The mirror with an image display function according to [3], wherein the circularly polarized light reflecting layer includes a ¼ wavelength plate and a linearly polarized light reflecting plate in this order from the high Re retardation film side.
[9] The half mirror includes a front plate,
The mirror with an image display function according to any one of [1] to [8], including the front plate, the high Re retardation film, and the reflective layer in this order.
[10] The half mirror includes a front plate,
The front plate is a laminated glass including two glass plates and an intermediate layer between the two glass plates,
The mirror with an image display function according to any one of [1] to [8], wherein the intermediate layer includes the high Re retardation film.
[11] The half mirror is a laminated glass including two glass plates and an intermediate layer between the two glass plates,
The mirror with an image display function according to any one of [1] to [8], wherein the intermediate layer includes the high Re retardation film and the reflective layer.

  The present invention provides a mirror with an image display function for a vehicle that can display a bright image and can observe a mirror reflection image without unevenness. When the mirror with an image display function of the present invention is used as an inner mirror of a vehicle, an external scenery through the rear glass can be observed as a mirror reflection image without unevenness.

Hereinafter, the present invention will be described in detail.
In the present specification, “to” is used to mean that the numerical values described before and after it are included as a lower limit value and an upper limit value. In the present specification, for example, an angle such as “45 °”, “parallel”, “vertical”, or “orthogonal”, unless otherwise specified, has a difference from an exact angle within a range of less than 5 degrees. Means. The difference from the exact angle is preferably less than 4 degrees, and more preferably less than 3 degrees.
In this specification, “(meth) acrylate” is used to mean “one or both of acrylate and methacrylate”.

In this specification, “selective” for circularly polarized light means that either the right circularly polarized light component or the left circularly polarized light component has more light than the other circularly polarized light component. Specifically, when referred to as “selective”, the degree of circular polarization of light is preferably 0.3 or more, more preferably 0.6 or more, and even more preferably 0.8 or more. More preferably, it is substantially 1.0. Table In _{/ (I R + I L)} | Here, the degree of circular polarization, the intensity of the right circularly polarized light component of the light I _R, when the strength of the left-handed circularly polarized light component and I _L, | I _R -I _L Is the value to be

  In this specification, “sense” for circularly polarized light means right circularly polarized light or left circularly polarized light. The sense of circularly polarized light is right-handed circularly polarized light when the electric field vector tip turns clockwise as time increases when viewed as the light travels toward you, and left when it turns counterclockwise. Defined as being circularly polarized.

  In this specification, the term “sense” may be used for the twist direction of the spiral of the cholesteric liquid crystal. The selective reflection by the cholesteric liquid crystal reflects right circularly polarized light when the twist direction (sense) of the cholesteric liquid crystal spiral is right, transmits left circularly polarized light, and reflects left circularly polarized light when the sense is left, Transmits circularly polarized light.

  Visible light is light having a wavelength visible to the human eye among electromagnetic waves, and indicates light having a wavelength range of 380 nm to 780 nm. Infrared rays (infrared light) are electromagnetic waves in the wavelength range that are longer than visible rays and shorter than radio waves. Among infrared rays, near infrared light is an electromagnetic wave having a wavelength range of 780 nm to 2500 nm.

  In this specification, the term “image” for a mirror with an image display function means an image that can be viewed and observed from the front side when the image is displayed on the image display unit of the image display device. Further, in this specification, the term “mirror reflection image” for a mirror with an image display function means an image that can be viewed and observed from the front side when no image is displayed on the image display unit of the image display device. .

  In the present specification, the front phase difference is a value measured using an AxoScan manufactured by Axometrix, or a value measured by a method described in Examples described later. In this specification, the front phase difference may be indicated as Re. The measurement wavelength of the front phase difference is 550 nm unless otherwise specified. When the front phase difference is a large value of about 5,000 or more, it is preferable to use a value measured by the method described in Examples described later. The front phase difference is a value measured by making light of a wavelength in the visible light wavelength region such as the central wavelength of selective reflection of the cholesteric liquid crystal layer incident in the film normal direction in KOBRA 21ADH or WR (manufactured by Oji Scientific Instruments). It can also be used. When selecting the measurement wavelength, the wavelength selection filter can be exchanged manually, or the measurement value can be converted by a program or the like.

  In this specification, the vehicle means a train, an automobile, and the like. As the vehicle, an automobile having a rear glass is particularly preferable.

<<<< Mirror with image display function for vehicles >>>>
The mirror with an image display function for a vehicle can be used, for example, as a vehicle rearview mirror (inner mirror). The mirror with an image display function for a vehicle may have a frame, a housing, a support arm for attaching to a vehicle body, and the like for use as a rearview mirror. Alternatively, the mirror with an image display function for a vehicle may be formed for incorporation into a room mirror. In the mirror with an image display function for a vehicle having the above-described shape, it is possible to specify the vertical and horizontal directions during normal use.

The mirror with an image display function for a vehicle may be a plate shape or a film shape, and may have a curved surface. The front surface of the vehicle image display function mirror may be flat or curved. It is possible to provide a wide mirror that can be viewed in a wide angle by making the convex curved surface the front side by curving. Such a curved front surface can be produced using a curved half mirror.
The curve may be in the vertical direction, the horizontal direction, or the vertical direction and the horizontal direction. Moreover, the curvature should just be a curvature radius of 500-3000 mm. More preferably, it is 1000-2500 mm. The radius of curvature is the radius of the circumscribed circle when the circumscribed circle of the curved portion is assumed in the cross section.

The mirror with an image display function of the present invention includes an image display device and a half mirror.
In the mirror with an image display function, an air layer may exist or an adhesive layer may exist between the image display device and the half mirror.
In the present specification, the surface on the half mirror side with respect to the image display device may be referred to as a front surface.
In this specification, “a mirror with an image display function for a vehicle” may be simply referred to as “a mirror with an image display function for a vehicle” or simply “a mirror with an image display function”.

<< Image display device >>
The image display device is not particularly limited. The image display device is preferably an image display device that emits (emits light) linearly polarized light to form an image, and more preferably a liquid crystal display device.
The liquid crystal display device may be a transmission type or a reflection type, and is particularly preferably a transmission type. The liquid crystal display device includes an IPS (In Plane Switching) mode, an FFS (Fringe Field Switching) mode, a VA (Vertical Alignment) mode, an ECB (Electrically Controlled Birefringence) mode, an STN (Super Twisted Nematic) mode, and a TN (Twisted Nematic) mode. Any liquid crystal display device such as an OCB (Optically Compensated Bend) mode may be used. The image display device preferably has an average visible light reflection of a wavelength of 380 to 780 nm of 30% or more and more preferably 40% or more when the power is turned off. The reflection of visible light when the image display device is turned off may be derived from the constituent members (such as a reflective polarizing plate and a backlight unit) of the image display device.

  The image displayed on the image display unit of the image display device may be a still image, a moving image, or simply text information. Further, it may be a monochrome display such as black and white, a multi-color display, or a full-color display. A preferable example of the image displayed on the image display unit of the image display device is an image taken by a vehicle-mounted camera. This image is preferably a moving image.

  For example, the image display device only needs to indicate the emission peak wavelength λR of red light, the emission peak wavelength λG of green light, and the emission peak wavelength λB of blue light in the emission spectrum during white display. By having such an emission peak wavelength, full-color image display is possible. λR may be any wavelength in the range of 580 to 700 nm, preferably in the range of 610 to 680 nm. λG may be any wavelength in the range of 500-580, preferably in the range of 510-550 nm. λB may be any wavelength in the range of 400-500 nm, preferably in the range of 440-480 nm.

<< Half Mirror >>
The half mirror may be plate-shaped or film-shaped, and may have a curved surface. The half mirror may be flat or curved. A curved half mirror can be produced using a curved front plate.
The half mirror includes a reflective layer and a high Re retardation film. The reflective layer and the high Re retardation film are preferably laminated with the same main surface area. In the present specification, “main surface” refers to the surface (front surface or back surface) of a plate-like or film-like member.

The half mirror may include other layers such as a front plate or an adhesive layer. When the half mirror includes a front plate, the front plate, the high Re retardation film, and the reflective layer are preferably in this order. When the half mirror includes a front plate, the area of the main surface of the front plate may be larger than the area of the main surface of the reflective layer, or may be the same or smaller. The reflective layer may be bonded to a part of the main surface of the front plate, and another type of reflective layer such as a metal foil may be bonded or formed at other portions. With such a configuration, an image can be displayed on a part of the mirror. On the other hand, a reflective layer may be bonded to the entire front plate main surface. Further, in the mirror with an image display function, a half mirror having a main surface having the same area as the image display unit of the image display device may be used, and has a main surface area larger or smaller than the image display unit of the image display device. A half mirror may be used. By selecting these relationships, it is possible to adjust the ratio and position of the surface of the image display unit with respect to the entire surface of the mirror.
Further, the half mirror may be a laminated glass, and the intermediate layer of the laminated glass may include a high Re retardation film and a reflective layer.
Although the film thickness of a half mirror is not specifically limited, It is preferable that it is 100 micrometers-20 mm, It is more preferable that it is 200 micrometers-15 mm, It is more preferable that it is 300 micrometers-10 mm.

<High Re retardation film>
The half mirror includes a high Re retardation film having a front phase difference of 5000 nm or more. In this specification, the term “high Re phase difference film” means a phase difference film having a high front phase difference, which is distinguished from a quarter wave plate (phase difference plate) described later. The front retardation of the high Re retardation film is preferably 6000 nm or more, and more preferably 8000 nm or more. The front retardation of the high Re retardation film is preferably as large as possible, but may be 100000 nm or less, 50000 nm or less, 40000 nm or less, or 30000 nm or less in consideration of manufacturing efficiency and thinning.

The high Re retardation film having a high front phase difference as described above can pseudo-polarize polarized light generated when sunlight passes through a vehicle window glass (particularly, rear glass).
The front phase difference that can make the polarized light pseudo-non-polarized is described in paragraphs [0022] to [0033] of JP-A-2005-321544. The specific numerical value of the front phase difference can be determined according to the vehicle using the mirror with an image display function of the present invention. In particular, it may be determined according to the magnitude of the front phase difference generated in the sunlight transmitted through the rear glass of the vehicle.

  It is known that tempered glass (for example, tempered glass which is not a laminated glass) used for vehicle window glass, particularly rear glass, has a birefringence distribution. The tempered glass is generally produced by heating a float plate glass to 700 ° C. near the softening point, and then rapidly cooling the glass surface by blowing air. This treatment lowers the temperature of the glass surface first and shrinks and solidifies, while the glass interior is slower to cool down than the surface and delays shrinking, resulting in stress distribution inside and no birefringence. Even when float glass is used, birefringence distribution occurs in the tempered glass.

  For this reason, it is considered that the above-described unevenness occurs in the mirror reflection image of light that passes through the rear glass of the vehicle in which the tempered glass produced as described above is used and enters the front surface of the mirror with an image display function. That is, when a polarization component with a distribution is generated in the light incident on the front surface of the mirror with the image display function due to the birefringence distribution, the reflected light on the front surface (outermost surface) of the mirror with the image display function and the selectively reflected light on the reflective layer It is considered that the difference in the intensity of reflected light is caused by the interference, causing the unevenness of the mirror reflection image described above. In the mirror with an image display function of the present invention, the light incident on the front surface of the mirror with the image display function is simulated before entering the reflection layer by using a high Re retardation film having a phase difference of a predetermined size. It is estimated that non-polarized light can reduce unevenness.

  In the mirror with an image display function, the high Re retardation film may be provided so that the high Re retardation film, the reflective layer, and the image display device are in this order. When the half mirror has a front plate, the front plate, the high Re retardation film, the reflective layer, and the image display device may be in this order. The front plate may also serve as a high Re retardation film.

  Examples of the high Re retardation film include a birefringent material such as a plastic film and a quartz plate. Examples of the plastic film include polyester films such as polyethylene terephthalate (PET), polycarbonate films, polyacetal films, and polyarylate films. JP-A-2013-257579, JP-A-2015-102636, and the like can be referred to for a retardation film mainly composed of PET and having a high retardation. Commercial products such as optical Cosmo Shine (registered trademark) super birefringence type (Toyobo) may be used.

  In general, plastic films with high phase difference are melt-extruded from resin, cast on drums, etc., and formed into a film shape. It can be formed by stretching at a magnification. In order to promote crystallization and increase the strength of the film, a heat treatment called “heat setting” may be performed at a temperature exceeding the stretching temperature after stretching.

  It should be noted that the above-described unevenness of the mirror reflection image can be eliminated by providing the high Re retardation film on the rear glass of the vehicle. At this time, the mirror with an image display function may not include the high Re retardation film. A total of the front phase difference of the retardation film provided on the rear glass of the vehicle and the front phase difference of the retardation film in the mirror with an image display function achieves a front phase difference of 5000 nm or more, and the generated polarization is eliminated. Also good.

<Reflective layer>
As the reflective layer, a reflective layer that can function as a transflective layer may be used. That is, the reflective layer functions so that an image is displayed on the front surface of the mirror with an image display function by transmitting light emitted from the image display device when displaying an image, while reflecting when not displaying an image. The layer may be any layer as long as it reflects at least part of incident light from the front surface direction and transmits reflected light from the image display device so that the front surface of the mirror with an image display function functions as a mirror.
A polarizing reflection layer is used as the reflection layer. The polarization reflection layer may be a linear polarization reflection layer or a circular polarization reflection layer.

[Linear polarization reflection layer]
As the linearly polarized light reflecting layer, for example, (i) a linearly polarized light reflecting plate having a multilayer structure, (ii) a polarizer in which thin films having different birefringence are laminated, (iii) a wire grid polarizer, (iv) a polarizing prism, (v ) Scattering anisotropic polarizing plate.

  (I) Examples of the linearly polarized light reflecting plate having a multilayer structure include those obtained by laminating a plurality of dielectric thin films having different refractive indexes. In order to obtain a wavelength selective reflection film, it is preferable to alternately stack a plurality of high-refractive-index dielectric thin films and low-refractive-index dielectric thin films. However, the number of types is not limited to two or more. It may be. The number of stacked layers is preferably 2 to 20 layers, more preferably 2 to 12 layers, still more preferably 4 to 10 layers, and particularly preferably 6 to 8 layers. When the number of stacked layers exceeds 20, the production efficiency may be reduced due to multilayer deposition, and the object and effect of the present invention may not be achieved.

  The order of stacking the dielectric thin films is not particularly limited and can be appropriately selected depending on the purpose. For example, when the refractive index of an adjacent film is high, a film having a lower refractive index is first stacked. . Conversely, when the refractive index of the adjacent layer is low, a film having a higher refractive index is first laminated. The boundary between high and low refractive index is 1.8. Note that whether the refractive index is high or low is not absolute. Among high-refractive-index materials, there may be a material with a relatively high refractive index and a material with a relatively low refractive index, which are used alternately. May be.

Examples of the material for the high refractive index dielectric thin film include Sb ₂ O ₃ , Sb ₂ S ₃ , Bi ₂ O ₃ , CeO ₂ , CeF ₃ , HfO ₂ , La ₂ O ₃ , Nd ₂ O ₃ , and Pr _6. O ₁₁ , Sc ₂ O ₃ , SiO, Ta ₂ O ₅ , TiO ₂ , TlCl, Y ₂ O ₃ , ZnSe, ZnS, ZrO ₂ and the like can be mentioned. Among these, Bi ₂ O ₃ , CeO ₂ , CeF ₃ , HfO ₂ , SiO, Ta ₂ O ₅ , TiO ₂ , Y ₂ O ₃ , ZnSe, ZnS, and ZrO ₂ are preferable, and among these, SiO, Ta ₂ O ₅ , TiO ₂ , Y ₂ O ₃ , ZnSe, ZnS, and ZrO ₂ are particularly preferable.

Examples of the material for the low refractive index dielectric thin film include Al ₂ O ₃ , BiF ₃ , CaF ₂ , LaF ₃ , PbCl ₂ , PbF ₂ , LiF, MgF ₂ , MgO, NdF ₃ , SiO ₂ , Si ₂ O. ₃ , NaF, ThO ₂ , ThF ₄ , and the like. Among these, Al ₂ O ₃ , BiF ₃ , CaF ₂ , MgF ₂ , MgO, SiO ₂ and Si ₂ O ₃ are preferable, and Al ₂ O ₃ , CaF ₂ , MgF ₂ , MgO, SiO ₂ and Si ₂ O ₃ are preferable. Is particularly preferred.
In the dielectric thin film material, the atomic ratio is not particularly limited and can be appropriately selected according to the purpose. The atomic ratio can be adjusted by changing the atmospheric gas concentration during film formation.

The method for forming the dielectric thin film is not particularly limited and may be appropriately selected depending on the purpose. For example, a vacuum vapor deposition method such as ion plating or ion beam, a physical vapor deposition method such as sputtering ( PVD method), chemical vapor deposition method (CVD method), and the like. Among these, the vacuum evaporation method and the sputtering method are preferable, and the sputtering method is particularly preferable.
As the sputtering method, a DC sputtering method having a high film formation rate is preferable. In the DC sputtering method, it is preferable to use a material having high conductivity.
As a method for forming a multilayer film by sputtering, for example, (1) a one-chamber method in which films are alternately or sequentially formed from a plurality of targets in one chamber, and (2) continuous film formation in a plurality of chambers. There is a multi-chamber method. Among these, the multi-chamber method is particularly preferable from the viewpoint of preventing productivity and material contamination.
The film thickness of the dielectric thin film is preferably λ / 16 to λ, more preferably λ / 8 to 3λ / 4, and more preferably λ / 6 to 3λ / 8 in the optical wavelength order.

  The light propagating in the dielectric deposition layer is determined by the product of the thickness of the dielectric thin film and the refractive index of the film with respect to the light due to multiple reflections of part of the light for each dielectric thin film. Only light of a wavelength is selectively transmitted. Further, the central transmission wavelength of the dielectric vapor deposition layer has an angle dependency with respect to the incident light, and the transmission wavelength can be changed by changing the incident light.

(Ii) As a polarizer in which thin films having different birefringence are laminated, for example, those described in JP-T-9-506837 can be used. Specifically, when processed under conditions selected to obtain a refractive index relationship, a polarizer can be formed using a wide variety of materials. In general, one of the first materials needs to have a different refractive index than the second material in the chosen direction. This difference in refractive index can be achieved in a variety of ways, including stretching, extrusion, or coating during or after film formation. Furthermore, it is preferred to have similar rheological properties (eg, melt viscosity) so that the two materials can be coextruded.
Commercially available products can be used as the polarizer in which thin films having different birefringence are laminated. Examples of commercially available products include DBEF (registered trademark) (manufactured by 3M).

(Iii) A wire grid type polarizer is a polarizer that transmits one of polarized light and reflects the other by birefringence of a fine metal wire.
The wire grid polarizer is a periodic arrangement of metal wires, and is mainly used as a polarizer in the terahertz wave band. In order for the wire grid to function as a polarizer, the wire interval needs to be sufficiently smaller than the wavelength of the incident electromagnetic wave.
In the wire grid polarizer, metal wires are arranged at equal intervals. The polarization component in the polarization direction parallel to the longitudinal direction of the metal wire is reflected by the wire grid polarizer, and the polarization component in the perpendicular polarization direction is transmitted through the wire grid polarizer.

  Commercially available products can be used as the wire grid polarizer, and examples of commercially available products include a wire grid polarizing filter 50 × 50, NT46-636 manufactured by Edmund Optics.

[Circularly polarized reflective layer]
By using a circularly polarized light reflection layer for the half mirror, incident light from the front side can be reflected as circularly polarized light, and incident light from the image display device can be transmitted as circularly polarized light. Therefore, in a mirror with an image display function using a circularly polarized reflection layer, a display image and a mirror reflection image can be observed without depending on the direction of the mirror with an image display function, even through polarized sunglasses.

  Examples of the circularly polarized light reflecting layer include a circularly polarized light reflecting layer including a linearly polarized light reflecting plate and a quarter wavelength plate and a circularly polarized light reflecting layer including a cholesteric liquid crystal layer (hereinafter, for the sake of distinction, “Polλ / 4 Circular polarization reflective layer "and" cholesteric circular polarization reflection layer ").

[Polλ / 4 circularly polarized reflective layer]
In the Pol λ / 4 circularly polarized light reflecting layer, the linearly polarized light reflecting plate and the quarter wavelength plate are arranged so that the slow axis of the λ / 4 wavelength plate is 45 ° with respect to the polarized light reflecting axis of the linearly polarized light reflecting plate. Just do it. Moreover, the quarter wave plate and the linearly polarized light reflecting plate may be bonded by, for example, an adhesive layer.
By using the Polλ / 4 circularly polarized light reflecting layer so that the linearly polarized light reflector is close to the image display device, the light for image display from the image display device can be efficiently converted into circularly polarized light. Thus, the light can be emitted from the front surface of the mirror with an image display function. When the light for image display from the image display device is linearly polarized light, the polarization reflection axis of the linearly polarized light reflecting plate may be adjusted so as to transmit this linearly polarized light.
The film thickness of the Polλ / 4 circularly polarized light reflecting layer is preferably in the range of 2.0 μm to 300 μm, more preferably in the range of 8.0 to 200 μm.
As the linearly polarized light reflecting plate, those described above as the linearly polarized light reflecting layer can be used.
As the quarter wavelength plate, a quarter wavelength plate described later can be used.

[Cholesteric circularly polarized reflective layer]
The cholesteric circularly polarized light reflection layer includes at least one cholesteric liquid crystal layer. The cholesteric liquid crystal layer included in the cholesteric circularly polarized light reflection layer may be any layer that exhibits selective reflection in the visible light region.
The circularly polarized light reflecting layer may include two or more cholesteric liquid crystal layers, and may include other layers such as an alignment layer. The circularly polarized light reflecting layer is preferably composed only of a cholesteric liquid crystal layer. Further, when the circularly polarized light reflection layer includes a plurality of cholesteric liquid crystal layers, it is preferable that they are in direct contact with adjacent cholesteric liquid crystal layers. The circularly polarized light reflection layer preferably includes three or more cholesteric liquid crystal layers such as three layers and four layers.
The film thickness of the cholesteric circularly polarized light reflective layer is preferably in the range of 2.0 μm to 300 μm, more preferably in the range of 8.0 to 200 μm.

In this specification, a cholesteric liquid crystal layer means a layer in which a cholesteric liquid crystal phase is fixed. The cholesteric liquid crystal layer is sometimes simply referred to as a liquid crystal layer.
The cholesteric liquid crystal phase selectively reflects circularly polarized light of either right circularly polarized light or left circularly polarized light in a specific wavelength region and selectively transmits circularly polarized light of the other sense. It is known to show. In this specification, the circularly polarized light selective reflection is sometimes simply referred to as selective reflection.

  Many films formed from a composition containing a polymerizable liquid crystal compound have been known as a film containing a layer in which a cholesteric liquid crystal phase exhibiting circularly polarized light selectively is fixed. You can refer to the technology.

  The cholesteric liquid crystal layer may be a layer in which the orientation of the liquid crystal compound in the cholesteric liquid crystal phase is maintained. Typically, the polymerizable liquid crystal compound is placed in the orientation state of the cholesteric liquid crystal phase and then irradiated with ultraviolet rays. Any layer may be used as long as it is polymerized and cured by heating or the like to form a layer having no fluidity, and at the same time, the layer is changed to a state in which the orientation is not changed by an external field or an external force. In the cholesteric liquid crystal layer, it is sufficient that the optical properties of the cholesteric liquid crystal phase are maintained in the layer, and the liquid crystal compound in the layer may no longer exhibit liquid crystallinity. For example, the polymerizable liquid crystal compound may have a high molecular weight due to a curing reaction and may no longer have liquid crystallinity.

The central wavelength λ of selective reflection of the cholesteric liquid crystal layer depends on the pitch P (= helical period) of the helical structure in the cholesteric phase, and follows the relationship between the average refractive index n of the cholesteric liquid crystal layer and λ = n × P. The selective reflection center wavelength and the half width of the cholesteric liquid crystal layer can be obtained as follows.
When the transmission spectrum of the light reflection layer (measured from the normal direction of the cholesteric liquid crystal layer) is measured using a spectrophotometer UV3150 (Shimadzu Corporation), a peak of reduced transmittance is observed in the selective reflection region. Of the two wavelengths having a transmittance of 1/2 the maximum peak height, the wavelength value on the short wave side is λ1 (nm) and the wavelength value on the long wave side is λ2 (nm). The center wavelength and half width of selective reflection can be expressed by the following equations.
Selective reflection center wavelength = (λ1 + λ2) / 2
Half width = (λ2−λ1)
The center wavelength λ of selective reflection possessed by the cholesteric liquid crystal layer, obtained as described above, usually coincides with the wavelength at the center of gravity of the reflection peak of the circularly polarized reflection spectrum measured from the normal direction of the cholesteric liquid crystal layer. In the present specification, the center wavelength of selective reflection means the center wavelength when measured from the normal direction of the cholesteric liquid crystal layer.
As can be seen from the above equation, the center wavelength of selective reflection can be adjusted by adjusting the pitch of the helical structure. The center wavelength λ can be adjusted in order to selectively reflect either the right circularly polarized light or the left circularly polarized light with respect to light of a desired wavelength by adjusting the n value and the P value.

When light is incident on the cholesteric liquid crystal layer at an angle, the center wavelength of selective reflection is shifted to the short wavelength side. Therefore, it is preferable to adjust n × P so that λ calculated according to the above formula λ = n × P becomes a long wavelength with respect to the wavelength of selective reflection required for image display. In the cholesteric liquid crystal layer having a refractive index n ₂ , the center wavelength of selective reflection when a light beam passes at an angle of θ ₂ with respect to the normal direction of the cholesteric liquid crystal layer (helical axis direction of the cholesteric liquid crystal layer) is λ _d . Λ _d is expressed by the following equation.
λ _d = n ₂ × P × cos θ ₂

In consideration of the above, by designing the center wavelength of selective reflection of the cholesteric liquid crystal layer included in the circularly polarized light reflecting layer, it is possible to prevent the visibility of the image from being viewed obliquely. Also, the visibility of the image from an oblique direction can be intentionally reduced. This is useful because, for example, it is possible to prevent peeping in a smartphone or a personal computer. Further, due to the selective reflection property described above, the mirror with an image display function of the present invention may appear in the image and the mirror reflection image viewed from an oblique direction. By including a cholesteric liquid crystal layer having a central wavelength of selective reflection in the infrared light region in the circularly polarized light reflecting layer, it is possible to prevent such a color. In this case, the center wavelength of selective reflection in the infrared region is specifically 780 to 900 nm, preferably 780 to 850 nm.
When a cholesteric liquid crystal layer having a central wavelength of selective reflection is provided in the infrared light region, it is preferable that the cholesteric liquid crystal layer having a central wavelength of selective reflection in the visible light region is closest to the image display device.

  Since the pitch of the cholesteric liquid crystal phase depends on the type of chiral agent used together with the polymerizable liquid crystal compound or the concentration of the chiral agent, the desired pitch can be obtained by adjusting these. For the method of measuring spiral sense and pitch, use the methods described in “Introduction to Liquid Crystal Chemistry Experiments”, edited by the Japanese Liquid Crystal Society, Sigma Publishing 2007, page 46, and “Liquid Crystal Handbook”, Liquid Crystal Handbook Editing Committee, page 196. be able to.

  In the mirror with an image display function of the present invention, the circularly polarized light reflection layer includes a cholesteric liquid crystal layer having a central wavelength of selective reflection in the wavelength range of red light and a cholesteric liquid crystal layer having a central wavelength of selective reflection in the wavelength range of green light. And a cholesteric liquid crystal layer having a center wavelength of selective reflection in the wavelength range of blue light. Examples of the reflective layer include a cholesteric liquid crystal layer having a central wavelength of selective reflection at 400 nm to 500 nm, a cholesteric liquid crystal layer having a central wavelength of selective reflection at 500 nm to 580 nm, and a cholesteric liquid crystal having a central wavelength of selective reflection at 580 nm to 700 nm. It is preferable to include a layer.

  Further, when the circularly polarized light reflection layer includes a plurality of cholesteric liquid crystal layers, it is preferable that the cholesteric liquid crystal layer closer to the image display device has a longer selective reflection center wavelength. With such a configuration, it is possible to suppress an oblique color tone in an image.

  In particular, in a mirror with an image display function using a cholesteric circularly polarized reflection layer that does not include a quarter-wave plate, the center wavelength of selective reflection that each cholesteric liquid crystal layer has is 5 nm or more with the wavelength of the emission peak of the image display device. It is preferable to make them different. This difference is more preferably 10 nm or more. By shifting the center wavelength of selective reflection and the wavelength of the emission peak for image display of the image display device, the light for image display is not reflected by the cholesteric liquid crystal layer, and the display image can be brightened. The wavelength of the emission peak of the image display device can be confirmed by the emission spectrum when the image display device displays white. The peak wavelength may be any peak wavelength in the visible light region of the emission spectrum. For example, the above-described red light emission peak wavelength λR, green light emission peak wavelength λG, and blue light emission peak wavelength λB of the image display device. Any one or more selected from the group consisting of: The central wavelength of selective reflection of the cholesteric liquid crystal layer is 5 nm or more for any of the above-described red light emission peak wavelength λR, green light emission peak wavelength λG, and blue light emission peak wavelength λB of the image display device, preferably It is preferably different by 10 nm or more. When the circularly polarized light reflection layer includes a plurality of cholesteric liquid crystal layers, the central wavelength of selective reflection of all the cholesteric liquid crystal layers is different from the wavelength of the peak of light emitted from the image display device by 5 nm or more, preferably 10 nm or more. do it. For example, when the image display device is a full-color display device showing an emission peak wavelength λR of red light, an emission peak wavelength λG of green light, and an emission peak wavelength λB of blue light in the emission spectrum during white display, All of the central wavelengths of selective reflection of the cholesteric liquid crystal layer may be different from each of λR, λG, and λB by 5 nm or more, preferably 10 nm or more.

  By adjusting the central wavelength of selective reflection of the cholesteric liquid crystal layer to be used according to the emission wavelength region of the image display device and the usage mode of the circularly polarized light reflection layer, a bright image can be displayed with high light utilization efficiency. Examples of the usage mode of the circularly polarized light reflecting layer include an incident angle of light to the circularly polarized light reflecting layer, an image observation direction, and the like.

  As each cholesteric liquid crystal layer, a cholesteric liquid crystal layer whose spiral sense is either right or left is used. The sense of reflected circularly polarized light in the cholesteric liquid crystal layer coincides with the sense of a spiral. The spiral senses of the plurality of cholesteric liquid crystal layers may all be the same or different. That is, either the right or left sense cholesteric liquid crystal layer may be included, or both the right and left sense cholesteric liquid crystal layers may be included. However, in the mirror with an image display function including a quarter wavelength plate, it is preferable that the spiral senses of the plurality of cholesteric liquid crystal layers are all the same. The spiral sense at that time may be determined according to the sense of circularly polarized light of the sense obtained as each cholesteric liquid crystal layer emitted from the image display device and transmitted through the quarter-wave plate. Specifically, a cholesteric liquid crystal layer having a spiral sense that transmits the circularly polarized light of the sense obtained from the image display device and transmitted through the quarter wavelength plate may be used.

The full width at half maximum Δλ (nm) of the selective reflection band showing selective reflection depends on the relationship of Δλ = Δn × P, where Δλ depends on the birefringence Δn of the liquid crystal compound and the pitch P. Therefore, the width of the selective reflection band can be controlled by adjusting Δn. Δn can be adjusted by adjusting the kind of the polymerizable liquid crystal compound and the mixing ratio thereof, or by controlling the temperature at the time of fixing the alignment.
In order to form one type of cholesteric liquid crystal layer having the same central wavelength of selective reflection, a plurality of cholesteric liquid crystal layers having the same period P and the same spiral sense may be stacked. By laminating cholesteric liquid crystal layers having the same period P and the same spiral sense, the circularly polarized light selectivity can be increased at a specific wavelength.

(¼ wavelength plate)
The mirror with an image display function using the cholesteric circularly polarized light reflection layer may further include a quarter wavelength plate.
By including a quarter-wave plate between the image display device and the cholesteric circularly polarized light reflection layer, in particular, the light from the image display device displaying an image by linearly polarized light is converted into circularly polarized light, and the cholesteric circularly polarized light is converted. It is possible to make the light incident on the reflective layer. Therefore, the light reflected by the circularly polarized light reflection layer and returning to the image display device side can be greatly reduced, and a bright image can be displayed. In addition, since a cholesteric circularly polarized light reflection layer can be configured not to generate sense circularly polarized light reflected to the image display device side by using a quarter wavelength plate, an image by multiple reflection between the image display device and the half mirror is possible. Display quality is unlikely to deteriorate.
That is, for example, the center wavelength of selective reflection of the cholesteric liquid crystal layer included in the cholesteric circularly polarizing reflection layer is substantially the same as the emission peak wavelength of blue light in the emission spectrum during white display of the image display device (for example, the difference is less than 5 nm). Even if it is, it can transmit the emitted light of an image display apparatus to the front side, without producing the circularly polarized light of the sense reflected in an image display side in a circularly polarized light reflection layer.

  The quarter-wave plate used in combination with the cholesteric circularly polarizing reflection layer is preferably angle-adjusted so that the image becomes brightest when bonded to the image display device. That is, the relationship between the polarization direction of the linearly polarized light (transmission axis) and the slow axis of the quarter-wave plate so that the linearly polarized light is transmitted best, particularly for an image display device displaying an image by linearly polarized light. Is preferably adjusted. For example, in the case of a single layer type quarter wave plate, it is preferable that the transmission axis and the slow axis form an angle of 45 °. The light emitted from the image display device displaying an image by linearly polarized light is circularly polarized light of either right or left sense after passing through the quarter wavelength plate. The circularly polarized light reflecting layer may be formed of a cholesteric liquid crystal layer having a twist direction that transmits the circularly polarized light having the above-described sense.

The quarter wave plate may be a retardation layer that functions as a quarter wave plate in the visible light region. Examples of the quarter-wave plate include a single-layer quarter-wave plate, a broadband quarter-wave plate in which a quarter-wave plate and a half-wave retardation plate are stacked, and the like.
The front phase difference of the former ¼ wavelength plate may be a length that is ¼ of the emission wavelength of the image display device. Therefore, for example, when the emission wavelength of the image display device is 450 nm, 530 nm, and 640 nm, the wavelength of 450 nm is 112.5 nm ± 10 nm, preferably 112.5 nm ± 5 nm, more preferably 112.5 nm, and 530 nm. Reverse dispersion such that the phase difference is 160 nm ± 10 nm, preferably 160 nm ± 5 nm, more preferably 160 nm at a wavelength of 5 nm ± 10 nm, preferably 132.5 nm ± 5 nm, more preferably 132.5 nm, 640 nm The retardation layer is most preferable as a quarter wavelength plate, but a retardation plate having a small retardation wavelength dispersion or a forward dispersion retardation plate can also be used. The reverse dispersion means a property that the absolute value of the phase difference becomes larger as the wavelength becomes longer, and the forward dispersion means a property that the absolute value of the phase difference becomes larger as the wavelength becomes shorter.

  The laminated quarter-wave plate is formed by laminating a quarter-wave plate and a half-wave retardation plate at an angle of 60 ° with the slow axis, and the side of the half-wave retardation plate is linearly polarized. It is arranged on the incident side and the slow axis of the half-wave retardation plate is used so as to cross 15 ° or 75 ° with respect to the polarization plane of the incident linearly polarized light. Can be suitably used because of its good resistance.

  There is no restriction | limiting in particular as (lambda) / 4 wavelength plate, According to the objective, it can select suitably. For example, quartz plate, stretched polycarbonate film, stretched norbornene-based polymer film, transparent film containing inorganic particles having birefringence such as strontium carbonate, and oblique deposition of inorganic dielectric on support Thin films and the like.

As the λ / 4 wavelength plate, for example, (1) a birefringent film having a large retardation and a birefringence having a small retardation described in JP-A-5-27118 and JP-A-5-27119 A retardation film obtained by laminating the optical films so that their optical axes are orthogonal to each other, (2) a polymer film described in JP-A-10-68816, having a λ / 4 wavelength at a specific wavelength; And a retardation film which can be obtained by laminating a polymer film made of the same material and having a λ / 2 wavelength at the same wavelength to obtain a λ / 4 wavelength in a wide wavelength region, (2) JP-A-10-90521 (2) International Publication No. 00/26705 pamphlet, which can achieve λ / 4 wavelength in a wide wavelength region by laminating two polymer films. A retardation plate capable of achieving λ / 4 wavelength in a wide wavelength region using the modified polycarbonate film described in (4), in a wide wavelength region using a cellulose acetate film described in International Publication No. 00/65384 pamphlet. Examples thereof include a retardation plate capable of achieving λ / 4 wavelength.
A commercially available product may be used as the λ / 4 wavelength plate. Examples of the commercially available product include Pure Ace (registered trademark) WR (polycarbonate film manufactured by Teijin Limited).

The quarter wavelength plate may be formed by arranging and fixing a polymerizable liquid crystal compound or a polymer liquid crystal compound. For example, for a quarter-wave plate, a liquid crystal composition is applied to the surface of a temporary support, an alignment film, or a front plate, and a polymerizable liquid crystal compound in the liquid crystal composition is formed into a nematic alignment in a liquid crystal state, and then photocrosslinked. It can be formed by immobilization by thermal crosslinking. Details of the liquid crystal composition or the production method will be described later. A quarter-wave plate is formed by applying a liquid crystal composition on a surface of a temporary support, an alignment film, or a front plate to form a nematic alignment in a liquid crystal state and then cooling the composition containing a polymer liquid crystal compound. It may be a layer obtained by immobilizing.
The λ / 4 wave plate may be adhered to the cholesteric circularly polarized light reflecting layer by an adhesive layer or may be in direct contact with the latter, but the latter is preferred.

(Method for producing quarter-wave plate formed from cholesteric liquid crystal layer and liquid crystal composition)
Hereinafter, a preparation material and a preparation method of a quarter-wave plate formed from a cholesteric liquid crystal layer and a liquid crystal composition will be described.
Examples of the material used for forming the quarter wavelength plate include a liquid crystal composition containing a polymerizable liquid crystal compound. Examples of the material used for forming the cholesteric liquid crystal layer include a liquid crystal composition containing a chiral agent (optically active compound). The cholesteric liquid crystal layer as a temporary support, a support, an alignment film, a high Re retardation film, and a lower layer is prepared by mixing the liquid crystal composition dissolved in a solvent or the like by further mixing with a surfactant or a polymerization initiator as necessary. The cholesteric liquid crystal layer or the quarter-wave plate can be formed by applying to a quarter-wave plate and the like, and after alignment aging, and then fixing by curing the liquid crystal composition.

-Polymerizable liquid crystal compound-
A rod-like liquid crystal compound may be used as the polymerizable liquid crystal compound.
Examples of the rod-like polymerizable liquid crystal compound include a rod-like nematic liquid crystal compound. Examples of rod-like nematic liquid crystal compounds include azomethines, azoxys, cyanobiphenyls, cyanophenyl esters, benzoic acid esters, cyclohexanecarboxylic acid phenyl esters, cyanophenylcyclohexanes, cyano-substituted phenylpyrimidines, alkoxy-substituted phenylpyrimidines. , Phenyldioxanes, tolanes and alkenylcyclohexylbenzonitriles are preferably used. Not only low-molecular liquid crystal compounds but also high-molecular liquid crystal compounds can be used.

  The polymerizable liquid crystal compound can be obtained by introducing a polymerizable group into the liquid crystal compound. Examples of the polymerizable group include an unsaturated polymerizable group, an epoxy group, and an aziridinyl group, preferably an unsaturated polymerizable group, and particularly preferably an ethylenically unsaturated polymerizable group. The polymerizable group can be introduced into the molecule of the liquid crystal compound by various methods. The number of polymerizable groups possessed by the polymerizable liquid crystal compound is preferably 1 to 6, more preferably 1 to 3. Examples of polymerizable liquid crystal compounds are described in Makromol. Chem. 190, 2255 (1989), Advanced Materials 5, 107 (1993), U.S. Pat. Nos. 4,683,327, 5,622,648, and 5,770,107, International Publication WO95 / 22586, WO95. / 24455, WO 97/00600, WO 98/23580, WO 98/52905, JP-A-1-272551, JP-A-6-16616, JP-A-7-110469, JP-A-11-80081, and JP-A-2001. -3282893 etc. are included. Two or more kinds of polymerizable liquid crystal compounds may be used in combination. When two or more kinds of polymerizable liquid crystal compounds are used in combination, the alignment temperature can be lowered.

  Moreover, it is preferable that the addition amount of the polymeric liquid crystal compound in a liquid-crystal composition is 80-99.9 mass% with respect to solid content mass (mass except a solvent) of a liquid-crystal composition, and 85-99. More preferably, it is 5 mass%, and it is especially preferable that it is 90-99 mass%.

-Chiral agent: optically active compound-
The material used for forming the cholesteric liquid crystal layer preferably contains a chiral agent. The chiral agent has a function of inducing a helical structure of a cholesteric liquid crystal phase. The chiral compound may be selected according to the purpose because the helical sense or helical pitch induced by the compound is different.
The chiral agent is not particularly limited, and known compounds (for example, liquid crystal device handbook, Chapter 3-4-3, TN, chiral agent for STN, page 199, Japan Society for the Promotion of Science, 142nd edition, 1989) Description), isosorbide, and isomannide derivatives can be used.
A chiral agent generally contains an asymmetric carbon atom, but an axially asymmetric compound or a planar asymmetric compound containing no asymmetric carbon atom can also be used as the chiral agent. Examples of the axial asymmetric compound or the planar asymmetric compound include binaphthyl, helicene, paracyclophane, and derivatives thereof. The chiral agent may have a polymerizable group. When both the chiral agent and the liquid crystal compound have a polymerizable group, they are derived from the repeating unit derived from the polymerizable liquid crystal compound and the chiral agent by a polymerization reaction between the polymerizable chiral agent and the polymerizable liquid crystal compound. A polymer having repeating units can be formed. In this aspect, the polymerizable group possessed by the polymerizable chiral agent is preferably the same group as the polymerizable group possessed by the polymerizable liquid crystal compound. Therefore, the polymerizable group of the chiral agent is also preferably an unsaturated polymerizable group, an epoxy group or an aziridinyl group, more preferably an unsaturated polymerizable group, and an ethylenically unsaturated polymerizable group. Particularly preferred.
The chiral agent may be a liquid crystal compound.

  The content of the chiral agent in the liquid crystal composition is preferably 0.01 mol% to 200 mol%, more preferably 1 mol% to 30 mol% of the amount of the polymerizable liquid crystal compound.

-Polymerization initiator-
The liquid crystal composition preferably contains a polymerization initiator. In the embodiment in which the polymerization reaction is advanced by ultraviolet irradiation, the polymerization initiator to be used is preferably a photopolymerization initiator that can start the polymerization reaction by ultraviolet irradiation. Examples of the photopolymerization initiator include α-carbonyl compounds (described in US Pat. Nos. 2,367,661 and 2,367,670), acyloin ether (described in US Pat. No. 2,448,828), α-hydrocarbon substituted aromatics. Group acyloin compounds (described in US Pat. No. 2,722,512), polynuclear quinone compounds (described in US Pat. Nos. 3,046,127 and 2,951,758), combinations of triarylimidazole dimers and p-aminophenyl ketone (US patents) No. 3549367), acridine and phenazine compounds (JP-A-60-105667, US Pat. No. 4,239,850), oxadiazole compounds (US Pat. No. 4,221,970), and the like. .
The content of the photopolymerization initiator in the liquid crystal composition is preferably 0.1 to 20% by mass, and preferably 0.5 to 5% by mass with respect to the content of the polymerizable liquid crystal compound. Further preferred.

-Crosslinking agent-
The liquid crystal composition may optionally contain a crosslinking agent in order to improve the film strength after curing and improve the durability. As the cross-linking agent, those that can be cured by ultraviolet rays, heat, moisture and the like can be suitably used.
There is no restriction | limiting in particular as a crosslinking agent, According to the objective, it can select suitably, For example, polyfunctional acrylate compounds, such as a trimethylol propane tri (meth) acrylate and pentaerythritol tri (meth) acrylate; Glycidyl (meth) acrylate , Epoxy compounds such as ethylene glycol diglycidyl ether; aziridine compounds such as 2,2-bishydroxymethylbutanol-tris [3- (1-aziridinyl) propionate], 4,4-bis (ethyleneiminocarbonylamino) diphenylmethane; hexa Isocyanate compounds such as methylene diisocyanate and biuret type isocyanate; polyoxazoline compounds having an oxazoline group in the side chain; vinyltrimethoxysilane, N- (2-aminoethyl) 3-aminopropylto Alkoxysilane compounds such as methoxy silane. Moreover, a well-known catalyst can be used according to the reactivity of a crosslinking agent, and productivity can be improved in addition to membrane strength and durability improvement. These may be used individually by 1 type and may use 2 or more types together.
3 mass%-20 mass% are preferable, and, as for content of a crosslinking agent, 5 mass%-15 mass% are more preferable. When the content of the crosslinking agent is 3% by mass or more, an effect of improving the crosslinking density can be obtained. Moreover, the stability of the layer formed can be maintained by setting it as 20 mass% or less.

-Orientation control agent-
In the liquid crystal composition, an alignment control agent that contributes to stable or rapid planar alignment may be added. Examples of the orientation control agent include fluorine (meth) acrylate polymers described in paragraphs [0018] to [0043] of JP-A-2007-272185, and paragraphs [0031] to [0034] of JP-A-2012-203237. Etc.] and the compounds represented by the formulas (I) to (IV).
In addition, as an orientation control agent, 1 type may be used independently and 2 or more types may be used together.

  The addition amount of the alignment control agent in the liquid crystal composition is preferably 0.01% by mass to 10% by mass, more preferably 0.01% by mass to 5% by mass with respect to the total mass of the polymerizable liquid crystal compound. 0.02% by mass to 1% by mass is particularly preferable.

-Other additives-
In addition, the liquid crystal composition may contain at least one selected from a surfactant for adjusting the surface tension of the coating film to make the film thickness uniform, and various additives such as a polymerizable monomer. . Further, in the liquid crystal composition, if necessary, a polymerization inhibitor, an antioxidant, an ultraviolet absorber, a light stabilizer, a colorant, metal oxide fine particles, and the like may be added as long as the optical performance is not deteriorated. Can be added.

-Solvent-
There is no restriction | limiting in particular as a solvent used for preparation of a liquid-crystal composition, Although it can select suitably according to the objective, An organic solvent is used preferably.
The organic solvent is not particularly limited and may be appropriately selected depending on the intended purpose. For example, ketones, alkyl halides, amides, sulfoxides, heterocyclic compounds, hydrocarbons, esters, ethers, etc. Is mentioned. These may be used individually by 1 type and may use 2 or more types together. Among these, ketones are particularly preferable in consideration of environmental load.

-Application, orientation, polymerization-
The method of applying the liquid crystal composition to the temporary support, the alignment film, the high Re retardation film, the quarter wavelength plate, the cholesteric liquid crystal layer as the lower layer is not particularly limited and may be appropriately selected according to the purpose. For example, wire bar coating method, curtain coating method, extrusion coating method, direct gravure coating method, reverse gravure coating method, die coating method, spin coating method, dip coating method, spray coating method, slide coating method, etc. . It can also be carried out by transferring a liquid crystal composition separately coated on a support. The liquid crystal molecules are aligned by heating the applied liquid crystal composition. In forming the cholesteric liquid crystal layer, cholesteric alignment may be performed, and in forming the quarter-wave plate, nematic alignment is preferable. In the cholesteric orientation, the heating temperature is preferably 200 ° C. or lower, and more preferably 130 ° C. or lower. By this alignment treatment, an optical thin film in which the polymerizable liquid crystal compound is twisted and aligned so as to have a helical axis in a direction substantially perpendicular to the film surface is obtained. In the case of nematic orientation, the heating temperature is preferably 50 ° C to 120 ° C, more preferably 60 ° C to 100 ° C.

The aligned liquid crystal compound can be further polymerized to cure the liquid crystal composition. The polymerization may be either thermal polymerization or photopolymerization by light irradiation, but photopolymerization is preferred. It is preferable to use ultraviolet rays for light irradiation. The irradiation energy is preferably ^{20mJ / cm 2 ~50J / cm 2} , 100mJ / cm 2 ~1,500mJ / cm 2 is more preferable. In order to accelerate the photopolymerization reaction, light irradiation may be performed under heating conditions or in a nitrogen atmosphere. The irradiation ultraviolet wavelength is preferably 350 nm to 430 nm. The polymerization reaction rate is preferably high from the viewpoint of stability, preferably 70% or more, and more preferably 80% or more. The polymerization reaction rate can be determined by measuring the consumption ratio of the polymerizable functional group using an IR absorption spectrum.

  The thickness of each cholesteric liquid crystal layer is not particularly limited as long as it exhibits the above characteristics, but is preferably in the range of 1.0 to 150 μm, more preferably in the range of 4.0 to 100 μm. Good. The thickness of the quarter wave plate formed from the liquid crystal composition is not particularly limited, but is preferably 0.2 to 10 μm, more preferably 0.5 to 2 μm.

-Temporary support, support, alignment layer-
The liquid crystal composition may be applied and layered on the surface of the temporary support or the alignment layer formed on the surface of the temporary support. The temporary support or the temporary support and the alignment layer may be peeled off after forming the layer.
Further, a support may be used particularly when forming a quarter wavelength plate. The support does not have to be peeled off after forming the layer. Examples of the temporary support and the support include polyester such as polyethylene terephthalate (PET), polycarbonate, acrylic resin, epoxy resin, polyurethane, polyamide, polyolefin, cellulose derivative, silicone, or glass plate. The temporary support body should just be peeled, for example after adhere | attaching a circularly-polarizing reflection layer on a front plate. The temporary support may function as a protective film after the circularly polarized reflective layer is bonded to the front plate and further until the circularly polarized reflective layer is bonded to the image display device.

The alignment layer has a rubbing treatment of organic compounds such as polymers (resins such as polyimide, polyvinyl alcohol, polyester, polyarylate, polyamideimide, polyetherimide, polyamide, modified polyamide), oblique deposition of inorganic compounds, and microgrooves. It can be provided by means such as formation of a layer or accumulation of an organic compound (for example, ω-tricosanoic acid, dioctadecylmethylammonium chloride, methyl stearylate) by the Langmuir-Blodgett method (LB film). Further, an alignment layer that generates an alignment function by application of an electric field, application of a magnetic field, or light irradiation may be used.
In particular, the alignment layer made of a polymer is preferably subjected to a rubbing treatment and then a liquid crystal composition is applied to the rubbing treatment surface. The rubbing treatment can be performed by rubbing the surface of the polymer layer with paper or cloth in a certain direction.
The liquid crystal composition may be applied to the surface of the temporary support without providing the alignment layer, or the surface obtained by rubbing the temporary support.
The thickness of the alignment layer is preferably 0.01 to 5 μm, and more preferably 0.05 to 2 μm.

-Laminated film of layers formed from polymerizable liquid crystal compounds-
When forming a multi-layer film composed of a plurality of cholesteric liquid crystal layers and a multi-layer film composed of a quarter-wave plate and a plurality of cholesteric liquid crystal layers, each is directly applied to the surface of the quarter-wave plate or the previous cholesteric liquid crystal layer. The liquid crystal composition containing a polymerizable liquid crystal compound or the like may be applied, and the steps of alignment and fixing may be repeated. A separately prepared quarter wave plate, cholesteric liquid crystal layer, or a laminate thereof is used with an adhesive or the like. However, the former is preferable. Usually, when an adhesive layer provided with a film thickness of 0.5 to 10 μm is used, interference unevenness derived from thickness unevenness of the adhesive layer may be observed. Therefore, it is preferable to laminate without using the adhesive layer. It is. In the laminated film of the cholesteric liquid crystal layer, the liquid crystal on the air interface side of the cholesteric liquid crystal layer formed earlier is formed by forming the next cholesteric liquid crystal layer so as to be in direct contact with the surface of the cholesteric liquid crystal layer formed earlier. This is because the orientation direction of the molecules matches the orientation direction of the liquid crystal molecules below the cholesteric liquid crystal layer formed thereon, and the polarization property of the laminate of the cholesteric liquid crystal layer is improved.

<Front plate>
The mirror with an image display function of the present invention may have a front plate.
The front plate may be flat or curved.
The front plate may be in direct contact with the high Re retardation film, or may be directly adhered by an adhesive layer or the like. It is preferable that they are directly bonded by an adhesive layer or the like.
The front plate is not particularly limited. As the front plate, a glass plate or a plastic film used for producing a normal mirror can be used. The front plate is preferably transparent in the visible light region. Here, “transparent in the visible light region” means that the light transmittance in the visible light region is 80% or more, preferably 85% or more. The light transmittance used as a measure of transparency is measured by measuring the total light transmittance and the amount of scattered light using the method described in JIS-K7105, that is, using an integrating sphere light transmittance measuring device, and diffusing transmission from the total light transmittance. It can be calculated by subtracting the rate. The front plate preferably has a small birefringence. For example, the front phase difference may be 20 nm or less, preferably less than 10 nm, and more preferably 5 nm or less. Examples of the plastic film include polyester such as polyethylene terephthalate (PET), polycarbonate, acrylic resin, epoxy resin, polyurethane, polyamide, polyolefin, cellulose derivative, and silicone.

  The curved front plate can be produced by a plastic processing method such as injection molding. In injection molding, for example, a resin product can be obtained by melting raw plastic pellets with heat, injecting them into a mold, and then cooling and solidifying.

  The film thickness of the front plate may be about 100 μm to 10 mm, preferably 200 μm to 5 mm, more preferably 500 μm to 2 mm, and further preferably 500 μm to 1000 μm.

  The front plate may also serve as a high Re retardation film. That is, the front plate may be a high Re retardation film having a front phase difference of 5000 nm or more. Specifically, a plastic plate or the like having a front retardation of 5000 nm or more may be the front plate, and a laminated glass including a high Re retardation film in the intermediate layer may be the front plate.

(Laminated glass with high Re retardation film in the intermediate layer)
Laminated glass includes two glass plates and an intermediate layer therebetween. For laminated glass, generally, an interlayer film sheet for laminated glass is sandwiched between two glass plates, and then heat treatment and pressure treatment (treatment with a rubber roller, etc.) are repeated several times, and finally an autoclave or the like. It can manufacture by the method of heat-processing on pressurization conditions using. Although there is no restriction | limiting in particular about the thickness of a glass plate, What is necessary is just about 0.5 mm-5 mm, 1 mm-3 mm are preferable and 2.0-2.3 mm are more preferable.

The laminated glass including the high Re retardation film in the intermediate layer may be formed through a normal laminated glass manufacturing process after the high Re retardation film is formed on the glass plate surface. At this time, the high Re retardation film may be bonded to a glass plate with an adhesive, for example.
In addition, the laminated glass including the high Re retardation film in the intermediate layer is subjected to the above heat treatment and pressure treatment using the laminated intermediate film sheet for laminated glass including the high Re retardation film as the intermediate film sheet. It may be formed. A laminated interlayer film for laminated glass including a high Re retardation film can be formed by bonding a high Re retardation film to the surface of a known interlayer film. Alternatively, a high Re retardation film can be formed between two known intermediate film sheets. The two interlayer sheets may be the same or different, but are preferably the same.

As the intermediate film sheet, for example, a resin film containing a resin selected from the group of polyvinyl butyral (PVB), ethylene-vinyl acetate copolymer, and chlorine-containing resin can be used. The resin is preferably a main component of the interlayer sheet. The main component means a component that occupies a ratio of 50% by mass or more of the interlayer film. Of the above resins, polyvinyl butyral or ethylene-vinyl acetate copolymer is preferable, and polyvinyl butyral is more preferable. The resin is preferably a synthetic resin.
Polyvinyl butyral can be obtained by acetalizing polyvinyl alcohol with butyraldehyde. The preferable lower limit of the degree of acetalization of the polyvinyl butyral is 40%, the preferable upper limit is 85%, the more preferable lower limit is 60%, and the more preferable upper limit is 75%.

The polyvinyl butyral can be prepared by acetalizing polyvinyl alcohol with butyraldehyde. Polyvinyl alcohol is usually obtained by saponifying polyvinyl acetate, and polyvinyl alcohol having a saponification degree of 80 to 99.8 mol% is generally used.
Moreover, the preferable minimum of the polymerization degree of the said polyvinyl alcohol is 200, and a preferable upper limit is 3000. If it is less than 200, the penetration resistance of the resulting laminated glass may be lowered, and if it exceeds 3000, the moldability of the resin film is deteriorated, and the rigidity of the resin film is excessively increased, resulting in poor workability. Sometimes. A more preferred lower limit is 500, and a more preferred upper limit is 2000.

A known bonding method can be used for bonding the high Re retardation film and the intermediate film, but it is preferable to use a laminating process. In order to prevent the high Re retardation film and the interlayer film from being peeled off after processing, it is preferable that the lamination process be performed under some heating and pressurizing conditions.
In order to perform lamination stably, the film surface temperature on the side to which the interlayer film sheet adheres is preferably 50 to 130 ° C, and more preferably 70 to 100 ° C.
It is preferable to apply pressure during lamination. Pressurization condition is preferably less than 2.0kg / cm ² (0.196MPa), more preferably in the range of 0.5~1.8kg / cm ² (0.049~0.176MPa) More preferably, it is in the range of 0.5 to 1.5 kg / cm ² (0.049 to 0.147 MPa).

<Adhesive layer>
The mirror with an image display function of the present invention includes a reflective layer and a high Re retardation film, a high Re retardation film and a front plate, an image display device and a reflective layer, a quarter wavelength plate and a linearly polarized light reflector, and other layers. An adhesive layer for adhesion may be included. The adhesive layer may be formed from an adhesive.
Adhesives include hot melt type, thermosetting type, photocuring type, reactive curing type, and pressure-sensitive adhesive type that does not require curing, from the viewpoint of curing method, and the materials are acrylate, urethane, urethane acrylate, epoxy , Epoxy acrylate, polyolefin, modified olefin, polypropylene, ethylene vinyl alcohol, vinyl chloride, chloroprene rubber, cyanoacrylate, polyamide, polyimide, polystyrene, polyvinyl butyral, etc. can do. From the viewpoint of workability and productivity, the photocuring type is preferable as the curing method, and from the viewpoint of optical transparency and heat resistance, the material is preferably an acrylate, urethane acrylate, epoxy acrylate, or the like. .

<Production method of half mirror>
What is necessary is just to produce a half mirror in the procedure according to the manufacturing method of the reflection layer to be used. A half mirror having a front plate may be produced by forming a high Re retardation film and a reflective layer on the front plate, or by bonding a separately prepared high Re retardation film and the reflective layer. It may be produced. For example, it may be produced by transferring a cholesteric circularly polarized light reflecting layer or a quarter wavelength plate and a cholesteric circularly polarized light reflecting layer formed on a temporary support to a high Re retardation film. For example, a cholesteric liquid crystal layer or a laminate of cholesteric liquid crystal layers is formed on a temporary support to form a cholesteric circularly polarized reflective layer, which is adhered to a high Re retardation film on the surface of this circularly polarized reflective layer, and then required Depending on the case, the temporary support can be peeled off to obtain a half mirror. Alternatively, a quarter-wave plate and a cholesteric liquid crystal layer are sequentially formed on the temporary support to form a laminate of the quarter-wave plate and the cholesteric circularly polarizing reflection layer, and this cholesteric liquid crystal layer (circularly polarized reflection) A half mirror can be obtained by adhering to a high Re retardation film on the surface of the layer and then peeling the temporary support as necessary.

  A half mirror of a laminated glass including a high Re retardation film and a reflective layer in an intermediate layer can be produced in the same manner as a laminated glass including a high Re retardation film in an intermediate layer. For example, a high Re retardation film and a reflective layer may be formed on a glass plate surface and then manufactured through a normal laminated glass manufacturing process. A laminated interlayer sheet for laminated glass including a high Re retardation film and a reflective layer may be produced. It may be used as an interlayer sheet. The laminated interlayer film for laminated glass including the high Re retardation film and the reflective layer can be formed by bonding the high Re retardation film and the reflective layer to the surface of a known interlayer film. Alternatively, the high Re retardation film and the reflective layer can be formed between two known intermediate film sheets. In the half mirror made of laminated glass, the high Re retardation film and the reflective layer may be in direct contact with each other or may be bonded through an adhesive layer.

<<< Method for manufacturing mirror with image display function >>>
The mirror with an image display function of the present invention is manufactured by arranging a half mirror such that the reflective layer side is the image display unit surface side of the image display device with respect to the high Re retardation film. When the half mirror has a front plate, the image display device, the reflective layer, the high Re retardation film, and the front plate are arranged in this order. Thereafter, the image display device and the half mirror may be integrated as necessary.
The integration of the image display device and the half mirror may be performed by connection with an outer frame or a hinge or adhesion.

  The present invention will be described more specifically with reference to the following examples. The materials, reagents, amounts and ratios of substances, operations, and the like shown in the following examples can be appropriately changed without departing from the gist of the present invention. Therefore, the scope of the present invention is not limited to the following examples.

<Production of retardation film (high Re retardation film)>
[Synthesis of raw material polyester]
(Raw material polyester 1)
As shown below, by directly reacting terephthalic acid and ethylene glycol to distill off water, esterify, and then use a direct esterification method in which polycondensation is performed under reduced pressure, raw polyester 1 ( Sb catalyst system PET) was obtained.

(1) Esterification reaction In a first esterification reaction tank, 4.7 tons of high-purity terephthalic acid and 1.8 tons of ethylene glycol are mixed over 90 minutes to form a slurry, and continuously at a flow rate of 3800 kg / h. To the first esterification reactor. Further, an ethylene glycol solution of antimony trioxide was continuously supplied, and the reaction was carried out at a reaction vessel temperature of 250 ° C. with stirring and an average residence time of about 4.3 hours. At this time, antimony trioxide was continuously added so that the amount of Sb added was 150 ppm in terms of element.

  This reaction product was transferred to a second esterification reaction vessel, and reacted with stirring at a temperature in the reaction vessel of 250 ° C. and an average residence time of 1.2 hours. To the second esterification reaction tank, an ethylene glycol solution of magnesium acetate and an ethylene glycol solution of trimethyl phosphate are continuously supplied so that the added amount of Mg and the added amount of P are 65 ppm and 35 ppm in terms of element, respectively. did.

(2) the polycondensation reaction above-obtained esterification reaction product supplied to the first polycondensation reaction vessel continuously stirring, the reaction temperature 270 ° C., the reaction vessel pressure 20 torr (2.67 × 10 ^{- 3} MPa) and polycondensation with an average residence time of about 1.8 hours.

Further, it was transferred to the second double condensation reaction tank, and while stirring in this reaction tank, the reaction tank temperature was 276 ° C., the reaction tank pressure was 5 torr (6.67 × 10 ⁻⁴ MPa), and the residence time was about 1.2 hours. The reaction (polycondensation) was performed under the conditions.

Subsequently, it was further transferred to the third triple condensation reaction tank. In this reaction tank, the reaction tank temperature was 278 ° C., the reaction tank pressure was 1.5 torr (2.0 × 10 ⁻⁴ MPa), and the residence time was 1.5 hours. The reaction product (polyethylene terephthalate (PET)) was obtained by reaction (polycondensation) under the following conditions.

  Next, the obtained reaction product was discharged into cold water in a strand form and immediately cut to prepare polyester pellets (cross section: major axis: about 4 mm, minor axis: about 2 mm, length: about 3 mm).

  The obtained polymer had IV (intrinsic viscosity) = 0.63. This polymer was designated as raw material polyester 1 (hereinafter abbreviated as PET1). The unit of intrinsic viscosity is dL / g.

(Raw material polyester 2)
10 parts by weight of the dried UV absorber (2,2 ′-(1,4-phenylene) bis (4H-3,1-benzoxazin-4-one), 90 parts by weight of PET1 (IV = 0.63) The mixture was mixed and pelletized in the same manner as the production of PET1 using a kneading extruder to obtain a raw material polyester 2 containing an ultraviolet absorber (hereinafter abbreviated as PET2).

[Production of polyester film]
-Film forming process-
After 90 parts by mass of PET 1 and 10 parts by mass of PET 2 containing an ultraviolet absorber were dried to a moisture content of 20 ppm or less, they were put into a hopper 1 of a single-screw kneading extruder 1 having a diameter of 50 mm. To 300 ° C. (intermediate layer II layer).
Moreover, after drying PET1 to a water content of 20 ppm or less, it was put into a hopper 2 of a single screw kneading extruder 2 having a diameter of 30 mm and melted at 300 ° C. by the extruder 2 (outer layer I layer, outer layer III layer).
These two kinds of polymer melts are respectively passed through a gear pump and a filter (pore diameter 20 μm), and then the polymer extruded from the extruder 1 is extruded into an intermediate layer (II layer) in a two-type three-layer confluence block. The polymer extruded from the machine 2 was laminated so as to be outer layers (I layer and III layer), and extruded from a die having a width of 120 mm into a sheet shape.

The molten resin was extruded from the die under the conditions that the pressure fluctuation was 1% and the temperature distribution of the molten resin was 2%. Specifically, the back pressure was increased by 1% with respect to the average pressure in the barrel of the extruder, and the piping temperature of the extruder was heated at a temperature 2% higher than the average temperature in the barrel of the extruder.
The molten resin extruded from the die was extruded onto a cooling cast drum set at a temperature of 25 ° C., and was brought into close contact with the cooling cast drum using an electrostatic application method. It peeled using the peeling roll arrange | positioned facing the cooling cast drum, and obtained the unstretched polyester film. At this time, the discharge amount of each extruder was adjusted so that the ratio of the thicknesses of the I layer, the II layer, and the III layer was 10:80:10. Moreover, the unstretched polyester film from which thickness differs was changed by changing the conditions which extrude molten resin from die | dye.

[Preparation of coating solution H]
A coating solution H was prepared with the composition shown below.
(Coating solution H)
Water 56.6 parts by mass acrylic resin (A1, solid content 28% by mass) 21.4 parts by mass carbodiimide compound: (B1, solid content 40% by mass) 2.9 parts by mass surfactant (E1, solid content 1% by mass) 8.1 parts by weight surfactant (E2, solid content 1% by weight aqueous solution) 9.6 parts by weight particles (F1, solid content 40% by weight) 0.4 parts by weight lubricant (G, solid content 30% by weight) 1.0 part by weight

Details of the compounds used are shown below.
Acrylic resin: (A1)
As the acrylic resin (A1), an aqueous dispersion of acrylic resin polymerized with monomers having the following composition (solid content: 28% by mass) was used.
Methyl methacrylate / styrene / 2-ethylhexyl acrylate / 2-hydroxyethyl methacrylate / acrylic acid = 59/9/26/5/1 (mass%) emulsion polymer (emulsifier: anionic surfactant), Tg = 45 ° C
Carbodiimide compound: (B1) (Nisshinbo, Carbodilite V-02-L2)
Surfactant: (E1) sulfosuccinic acid surfactant (manufactured by NOF Corporation, Rapisol A-90)
-Surfactant: (E2) Polyethylene oxide surfactant (Sanyo Chemical Industries, NAROACTY CL-95)
-Particles: (F1) Silica sol with an average particle size of 50 nm-Lubricant: (G) Carnauba wax

[Formation of retardation film]
(Formation of uniaxially stretched (transversely stretched) film (retardation films AD))
By the reverse roll method, the coating liquid H having the above composition was applied to both sides of the unstretched polyester film while adjusting the coating amount after drying to be 0.12 g / m ² . The obtained film is guided to a tenter (transverse stretching machine), heated to a preheating temperature of 92 ° C. while being gripped by a clip, and stretched 4.0 times in the width direction (stretching speed: 900). % / Min) to obtain a 5 m wide film. Next, the film surface temperature of the polyester film was controlled to 160 ° C., heat-fixed and relaxed, and then cooled at a cooling temperature of 50 ° C.

   After cooling, the polyester film was divided into 1.4 m widths in the width direction, and the chuck portion was trimmed. Then, after extruding (knurling) at a width of 10 mm on both ends of each divided roll, it was wound up 2000 m at a tension of 18 kg / m. The divided samples were designated as an end A, a center B, and an end C from one end side, and the center B was used.

(Formation of biaxially stretched (longitudinal / laterally stretched) film (retardation film E))
An unstretched polyester film is heated to 90 ° C. using a heated roll group and an infrared heater, and then stretched 3.1 times in the film running direction in a roll group having a difference in peripheral speed, and then stretched by a reverse roll method. The coating liquid H was applied to both sides of the film while adjusting the coating amount after drying so that both sides were 0.12 g / m ² . The film on which this coating film was formed was guided to a tenter, heated to a preheatable temperature of 125 ° C. while being gripped with a clip, and stretched 4.0 times in the width direction. Next, heat setting was performed so that the film surface temperature was 230 ° C. Otherwise, the retardation film E was produced in the same manner as the uniaxially stretched film.
Table 1 shows the thicknesses and Re of the produced retardation films A to E.

Re shown in Table 1 was measured as shown below.
Using two polarizing plates, the orientation axis direction of the film was determined, and a 4 cm × 2 cm rectangle was cut out so that the orientation axis directions were perpendicular to each other, and used as a measurement sample. For this sample, the biaxial refractive index (Nx, Ny) perpendicular to each other and the refractive index (Nz) in the thickness direction were determined by an Abbe refractometer (NAGO-4T, measurement wavelength 589 nm, manufactured by Atago Co., Ltd.). The absolute value of the refractive index difference (| Nx−Ny |) was defined as the refractive index anisotropy (ΔNxy). The thickness d (nm) of the film was measured using an electric micrometer (manufactured by Fine Reef, Millitron 1245D), and the unit was converted to nm. The front phase difference (Re) was determined from the product (ΔNxy × d) of refractive index anisotropy (ΔNxy) and film thickness d (nm).

<Preparation of reflective layer (cholesteric liquid crystal film)>
(1) Coating liquid 1 was prepared for a quarter-wave plate, and coating liquid 2, coating liquid 3, and coating liquid 4 were prepared with the compositions shown in Table 2 below for forming a cholesteric liquid crystal layer.

Compound 2 was produced by the method described in JP-A-2005-99248.

(2) The temporary support (280 mm × 85 mm) uses a Toyobo Co., Ltd. PET film (Cosmo Shine A4100, thickness: 100 μm), and is rubbed (rayon cloth, pressure: 0.1 kgf (0.98 N), rotating. Number: 1000 rpm, conveyance speed: 10 m / min, number of times: 1 reciprocation).
(2) The coating liquid 1 was applied to the rubbed surface of the PET film using a wire bar, then dried and placed on a hot plate at 30 ° C., and an electrodeless lamp “D bulb” (60 mW / cm ² ), UV irradiation was performed for 6 seconds, and the liquid crystal phase was fixed to obtain a quarter wavelength plate having a thickness of 0.8 μm. The coating liquid 2 is applied to the surface of the obtained layer using a wire bar, dried and placed on a hot plate at 30 ° C., and an electrodeless lamp “D bulb” (60 mW / cm ² ) manufactured by Fusion UV Systems Co., Ltd. Was irradiated with UV for 6 seconds to fix the cholesteric liquid crystal phase to obtain a cholesteric liquid crystal layer having a thickness of 3.5 μm. Further, the same steps were repeated using the coating solution 3 and the coating solution 4, and a laminate A of the quarter wavelength plate and the three cholesteric liquid crystal layers (the layer of the coating solution 3: 3.0 μm, the layer of the coating solution 4: 2.7 μm) was obtained. When the transmission spectrum of the laminate A was measured with a spectrophotometer (manufactured by JASCO Corporation, V-670), transmission spectra having center wavelengths of selective reflection at 630 nm, 540 nm, and 450 nm were obtained.

<Preparation of reflective layer (reflective linear polarizing plate)>
A linearly polarized light reflector was prepared based on the method described in JP-T-9-506837. A 2,6-polyethylene naphthalate (PEN) and naphthalate 70 / terephthalate 30 copolyester (coPEN) was synthesized in a standard polyester resin synthesis kettle using ethylene glycol as the diol. A single layer film of PEN and coPEN was extruded and then stretched at a stretch ratio of 5: 1 at about 150 ° C. It was confirmed that the refractive index of PEN with respect to the orientation axis was about 1.88, the refractive index with respect to the transverse axis was 1.64, and the refractive index of the coPEN film was about 1.64.
Then, the thickness of the alternating layer of PEN and coPEN was formed in the film thickness shown in Table 3 (1) by co-extrusion using a 50 slot supply block supplied with a standard extrusion die. By repeating the above, the PEN and coPEN layers shown in Tables 3 (2) to (5) were formed in order, and the formation of the layers (1) to (5) was repeated until a total of 250 layers each. Laminated. Thereafter, the stretched film was thermally cured at about 230 ° C. for 30 seconds in an air oven to obtain a laminate B.

<Formation of half mirror>
The phase difference film A is sandwiched between polyvinyl butyral interlayer sheets (thickness: 380 μm) for laminated glass and laminated (heating temperature: 80 ° C., pressure: 1.5 kg / cm ² (0.147 MPa), conveyance speed: 0. 1 m / min) to produce a laminated interlayer sheet for laminated glass.
Next, the laminated interlayer film for laminated glass prepared above was sandwiched between two blue plate glasses (250 mm × 75 mm, thickness: 0.7 mm), placed in a rubber bag, and decompressed with a vacuum pump. Thereafter, the temperature was raised to 90 ° C. under reduced pressure, held for 30 minutes, and then returned to normal temperature and pressure. Thereafter, it was kept in an autoclave for 20 minutes under conditions of a pressure of 1.3 MPa and a temperature of 130 ° C. This was returned to room temperature and normal pressure to produce a laminated glass including a high Re retardation film in the intermediate layer.

Next, an adhesive LCR0631 manufactured by Toa Gosei Co., Ltd. was applied to the surface of the cholesteric liquid crystal layer of the laminate A with a wire bar, and then bonded to the surface of the laminated glass using a laminator. At this time, the count of the wire bar and the nip roll pressure of the laminator were adjusted, and the thickness of the adhesive layer was adjusted to 2 μm. After that, after placing on a hot plate at 50 ° C. and irradiating with UV for 30 seconds with an electrodeless lamp “D bulb” (60 mW / cm ² ) manufactured by Fusion UV Systems, the PET film was peeled off, The half mirror of Example 1 was obtained.

  In place of the retardation film A and the laminate A, Examples 2 to 4 and the comparison were made in the same manner as the production of the half mirror of Example 1, except that the high Re retardation film and the reflective layer shown in Table 3 were used. Half mirrors of Examples 1 to 4 were produced.

<Production of mirror with image display function>
The half mirror produced above is adhered to the surface of the image display unit of the image display device (iPad (registered trademark) Retina) so that the glass plate, the retardation film, the reflective layer, and the image display device are in this order. An attached mirror was produced. At this time, the quarter-wave plate in the reflection layer was arranged so that the slow axis of the quarter-wave plate was inclined by 45 degrees with respect to the transmission axis of the image display device (the polarization direction of light emission of the LCD).

<Evaluation of mirror with image display function>
The produced mirror with an image display function was attached to the position of the inner mirror of a vehicle (vehicle type: Honda 2002 Step Wagon). An image of the image display device and a mirror reflection image that can be confirmed in a state where sunlight is incident on the position of the inner mirror from the rear glass of the vehicle were evaluated according to the following criteria. The results are shown in Table 4.
[image]
A: Bright image without distortion B: Image with distortion, light / dark unevenness, or dark image overall [unevenness (derived from rear glass birefringence)]
A: Oblique light / dark unevenness of oblique line light is not visible B: Uneven light / dark unevenness of oblique light is visible [unevenness (derived from retardation film)]
A: Spotted color unevenness or oblique color unevenness is not visible B: Spotted color unevenness or oblique color unevenness is visible As a result, in Examples 1 to 5, unevenness derived from rear glass birefringence cannot be visually recognized. And no unevenness derived from the retardation film was seen.

Claims (11)

A mirror with an image display function for a vehicle,
Including half mirror and image display device,
The half mirror includes a high Re retardation film and a reflective layer,
In the mirror with an image display function, the high Re retardation film, the reflective layer, and the image display device are arranged in this order,
The high Re retardation film has a front phase difference of 5000 nm or more,
The mirror with an image display function, wherein the reflective layer is a linearly polarized light reflective layer or a circularly polarized light reflective layer. The mirror with an image display function according to claim 1, wherein the front phase difference is 7000 nm or more. The mirror with an image display function according to claim 1, wherein the reflective layer is a circularly polarized reflective layer. The mirror with an image display function according to claim 3, wherein the circularly polarized light reflection layer includes a cholesteric liquid crystal layer. The mirror with an image display function according to claim 4, wherein the circularly polarized light reflection layer includes three or more cholesteric liquid crystal layers. Including a quarter wave plate,
The mirror with an image display function according to claim 4 or 5, wherein the half mirror includes the high Re retardation film, the circularly polarizing reflection layer, and the quarter wavelength plate in this order. The mirror with an image display function according to claim 6, wherein the circularly polarized light reflection layer and the quarter-wave plate are in direct contact with each other. The mirror with an image display function according to claim 3, wherein the circularly polarized light reflection layer includes a quarter-wave plate and a linearly polarized light reflection plate in this order from the high Re retardation film side. The half mirror includes a front plate,
The mirror with an image display function according to any one of claims 1 to 8, comprising the front plate, the high Re retardation film, and the reflective layer in this order. The half mirror includes a front plate,
The front plate is a laminated glass including two glass plates and an intermediate layer between the two glass plates,
The mirror with an image display function according to claim 1, wherein the intermediate layer includes the high Re retardation film. The half mirror is a laminated glass including two glass plates and an intermediate layer between the two glass plates,
The mirror with an image display function according to claim 1, wherein the intermediate layer includes the high Re retardation film and the reflective layer.