JP6536712B2 - Optical sheet and optical component - Google Patents

Description

  The present invention relates to an optical sheet and an optical component.

  For example, there is known an optical sheet which absorbs a specific wavelength range from incident light for the purpose of enhancing the contrast of a visual field, antiglare and the like (see, for example, Patent Document 1). This optical sheet is used by being attached to glasses, sunglasses, a sun visor or the like.

  The optical sheet described in Patent Document 1 includes, for example, a resin material, and a dye (a light absorbing agent) contained in the resin material and absorbing light of a specific wavelength in the visible light region. The optical sheet is formed into, for example, a sheet by blending a dye in a molten resin material, extruding in that state, and then cooling.

  However, the dye (light absorbing agent) may be deteriorated by ultraviolet light, for example, when it is used outdoors.

WO 2014/115705

  An object of the present invention is to provide an optical sheet and an optical component which can prevent a light absorber (visible light absorber) from being deteriorated by ultraviolet light.

Such an object is achieved by the present invention of the following (1) to (5).
(1) 350 nm or more and 740 nm or more mainly using polycarbonate having a viscosity average molecular weight Mv of 24000 or more and 27500 or less and a melt flow rate measured according to JIS K 7210 of 5.3 g / 10 min or more and 25 g / 10 min or less It has a specific wavelength absorbing layer containing a light absorbing agent that absorbs light of a specific wavelength among light in the following wavelength range, and an ultraviolet light absorbing agent that absorbs light of a wavelength of 100 nm to 420 nm ,
The melting point of the light absorber is 300 ° C. or more and 400 ° C. or less,
The content of the light absorbing agent before Symbol specific wavelength absorbing layer is less than 0.003 wt% 4 wt%,
The content of the ultraviolet light absorber in the specific wavelength absorption layer is greater than the content of the light absorber in the specific wavelength absorption layer, and is 0.07 wt% or more and 6 wt% or less. Sheet.

( 2 ) The optical sheet according to (1) , wherein the polycarbonate has a water absorption of 0.02% or more and 0.2% or less.

( 3 ) The optical sheet according to (1) or (2) , wherein the melting point T1 of the polycarbonate is smaller than the melting point T2 of the light absorbing agent and the melting point T3 of the ultraviolet light absorbing agent.

( 4 ) The optical sheet according to any one of (1) to (3) , wherein the specific wavelength absorbing layer has a degree of stretching of 10% or less.

( 5 ) base material,
An optical component comprising: the optical sheet according to any one of the above (1) to (4) , which is laminated on the base material.

  According to the present invention, it is possible to provide an optical sheet and an optical component which can prevent the light absorber (visible light absorber) and the ultraviolet absorber from aggregating.

It is a perspective view of a sunglasses provided with an optical sheet (a 1st embodiment) of the present invention. It is a perspective view of a sun visor provided with an optical sheet (the 1st embodiment) of the present invention. It is the side view which showed typically the optical sheet manufacturing apparatus which manufactures the optical sheet shown in FIG. It is sectional drawing which showed typically the optical component manufacturing apparatus which manufactures the optical sheet optical component shown in FIG. It is sectional drawing of the optical component shown in FIG. It is sectional drawing of an optical component provided with the optical sheet (2nd Embodiment) of this invention.

  Hereinafter, the polarizing laminate of the present invention will be described in detail based on the preferred embodiments shown in the attached drawings.

Embodiment
FIG. 1 is a perspective view of a sunglasses provided with an optical sheet (first embodiment) of the present invention. FIG. 2 is a perspective view of a sun visor provided with the optical sheet (first embodiment) of the present invention. FIG. 5 is a cross-sectional view of the optical component shown in FIG.

  Note that in FIGS. 1, 2 and 5 (as well as in FIG. 6), the upper side is referred to as "upper" or "upper", and the lower side is also referred to as "lower" or "lower". Further, in the drawings referred to in the present specification, the dimensions in the thickness direction are illustrated exaggeratingly, and they are greatly different from the actual dimensions.

  The optical sheet 1 of the present invention shown in FIG. 1, FIG. 2 and FIG. 5 is mainly composed of polycarbonate, and a light absorbing agent which absorbs light of a specific wavelength among light in a wavelength range of 350 nm to 740 nm and Has a specific wavelength absorbing layer 11 containing light of 100 nm or more and 420 nm or less, and the content of the ultraviolet light absorbing agent in the specific wavelength absorbing layer 11 is the light absorption in the specific wavelength absorbing layer 11 More than the content of the agent. Thus, the optical sheet 1 can absorb light of a specific wavelength range of visible light and can absorb ultraviolet light. In particular, the light absorbing agent is relatively susceptible to deterioration by ultraviolet light, but this deterioration can be prevented. Further, since the content of the ultraviolet light absorber in the specific wavelength absorption layer 11 is larger than the content of the light absorber in the specific wavelength absorption layer 11, the light absorber is more reliably prevented from being deteriorated by ultraviolet light. be able to.

  Such an optical sheet 1 is used for the sunglasses (optical component 10) shown in FIG. 1 and the sun visor (optical component 10 ') shown in FIG.

  As shown in FIG. 1, the sunglasses (optical component 10) include a frame 2 mounted on the head of the user and a lens 3 with an optical sheet (optical component) fixed to the frame 2. In the present specification, "lens" includes both those having a light collecting function and those not having a light collecting function.

  As shown in FIG. 1, the frame 2 is to be mounted on the head of the user, and the rim portion 21, the bridge portion 22, the temple portion 23 to be hung on the user's ear, and the nose pad portion 24. have. Each rim portion 21 has a ring shape, and is a portion on which the lens 3 with an optical sheet is mounted.

  The bridge portion 22 is a portion that connects the rim portions 21. The temple portion 23 has a shape of a temple and is connected to the edge of each rim portion 21. The temple portion 23 is a portion to be hung on the user's ear. The nose pad portion 24 is a portion that comes in contact with the nose of the user in a wearing state in which the sunglasses (optical component 10) are mounted on the head of the user. Thereby, the mounting state can be stably maintained.

  The shape of the frame 2 is not limited to that shown in the drawings as long as it can be mounted on the head of the user.

  The optical component of the present invention has a lens 4 (base material) and an optical sheet 1 laminated on the surface of the lens 4 on the front side (the side opposite to the human eye in the mounted state). Thereby, the function as a sunglasses can be exhibited, enjoying the advantage of the optical sheet 1 mentioned above.

  As shown in FIG. 2, the sun visor (optical component 10 ′) has a ring-shaped mounting portion 5 mounted on the head of the user and a flange 6 provided in front of the mounting portion 5. There is. The flange 6 has a light transmitting member 7 (base material) and an optical sheet 1 provided on the upper surface of the light transmitting member 7. Thereby, the function as a sun visor can be exhibited, enjoying the advantage of optical sheet 1 mentioned above.

  The constituent materials of the lens 4 and the light transmitting member 7 are not particularly limited as long as they have light transmitting properties, and various resin materials, various glasses and the like can be mentioned. Preferably it is polycarbonate. Thereby, the adhesion between the lens 4 or the light transmitting member 7 and the optical sheet 1 can be enhanced.

  The optical sheet 1 will be described in detail below. In addition, below, the case where it laminates | stacks on the lens 4 (base material) is demonstrated typically.

  As shown in FIG. 5, the optical sheet 1 has a specific wavelength absorbing layer 11. The specific wavelength absorbing layer 11 is mainly made of polycarbonate and contains a light absorbing agent and an ultraviolet light absorbing agent.

<Polycarbonate>
The polycarbonate is not particularly limited, and various polycarbonates can be used. Among them, an aromatic polycarbonate is preferable. The aromatic polycarbonate is provided with an aromatic ring in its main chain, whereby the strength of the optical sheet 1 can be made more excellent.

  This aromatic polycarbonate is synthesized, for example, by interfacial polycondensation reaction of bisphenol and phosgene, and transesterification reaction of bisphenol and diphenyl carbonate.

  Examples of the bisphenol include bisphenol A and bisphenol (modified bisphenol) as a source of a repeating unit of polycarbonate represented by the following formula (1).

（式（１）中、Ｘは、炭素数１〜１８のアルキル基、芳香族基または環状脂肪族基であり、ＲａおよびＲｂは、それぞれ独立して、炭素数１〜１２のアルキル基であり、ｍおよびｎは、それぞれ０〜４の整数であり、ｐは、繰り返し単位の数である。）

(In the formula (1), X is an alkyl group having 1 to 18 carbon atoms, an aromatic group or a cyclic aliphatic group, and Ra and Rb are each independently an alkyl group having 1 to 12 carbon atoms. , M and n are each an integer of 0 to 4, and p is the number of repeating units.)

  Specifically, examples of the bisphenol which is the source of the repeating unit of polycarbonate represented by the formula (1) include 4,4 ′-(pentane-2,2-diyl) diphenol and 4,4 ′-(4) Pentane-3,3-diyl) diphenol, 4,4 ′-(butane-2,2-diyl) diphenol, 1,1 ′-(cyclohexanediyl) diphenol, 2-cyclohexyl-1,4-bis ( 4-hydroxyphenyl) benzene, 2,3-biscyclohexyl-1,4-bis (4-hydroxyphenyl) benzene, 1,1'-bis (4-hydroxy-3-methylphenyl) cyclohexane, 2,2'- Examples thereof include bis (4-hydroxy-3-methylphenyl) propane and the like, and one or more of these can be used in combination.

  In particular, as the polycarbonate, it is preferable to use a bisphenol-type polycarbonate having a skeleton derived from bisphenol as a main component. By using such a bisphenol-type polycarbonate, the optical sheet 1 exhibits a further excellent strength.

  The average molecular weight of such a polycarbonate is preferably such that the viscosity average molecular weight Mv is from 20,000 to 30,000, more preferably from 23,000 to 28,000, and particularly preferably from 24,000 to 27,500. Thereby, the strength of the optical sheet 1 can be sufficiently increased. In addition, the fluidity can be sufficiently enhanced in the molten state of polycarbonate. Thereby, when manufacturing the optical sheet 1 by extrusion molding, for example, extrusion molding can be performed in the state which mixed the polycarbonate of a molten state and the light absorbing agent sufficiently. Accordingly, it is possible to prevent the light absorbent from being excessively aggregated after molding. Furthermore, by setting the viscosity average molecular weight Mv of the polycarbonate to the above-mentioned numerical range, it has sufficient strength. As a result, the light absorber is prevented from being aggregated and has sufficient strength.

  If the viscosity average molecular weight Mv of the polycarbonate is too small, there is a possibility that sufficient strength can not be obtained after molding. On the other hand, when the viscosity average molecular weight Mv of the polycarbonate is too large, the fluidity can not be sufficiently improved in the molten state. For this reason, there is a possibility that the mixing of the molten polycarbonate and the light absorbing agent becomes insufficient.

  The polycarbonate preferably has a melt flow rate (MFR) of 3 g / 10 min or more and 30 g / 10 min or less, more preferably 15 g / 10 min or more and 25 g / 10 min or less, which is measured in accordance with JIS K 7210 . Thereby, the fluidity of the polycarbonate can be sufficiently enhanced in the molten state. Therefore, for example, when manufacturing the optical sheet 1 by extrusion molding, extrusion molding can be performed in the state in which the polycarbonate in the molten state and the light absorbing agent are sufficiently mixed.

  The polycarbonate preferably has a water absorption of 0.02% or more and 0.2% or less, more preferably 0.04% or more and 0.15% or less. Thereby, extrusion molding can be performed in the state in which the polycarbonate in the molten state and the light absorbing agent are sufficiently mixed. Thus, excessive aggregation of the light absorbing agent can be prevented.

  The water absorption rate in the present specification is a value measured by Aquatrack 3E (manufactured by Brabender).

  Further, the content of the polycarbonate in the specific wavelength absorbing layer 11 is preferably 87 wt% or more and 99.949 wt% or less, and more preferably 90 wt% or more and 99.87 wt% or less. Thereby, the effects of the present invention can be more reliably exhibited.

<Light Absorbent>
The light absorbing agent is one that absorbs light of a specific wavelength. In the present specification, “to absorb light” means that the value of the maximum absorption wavelength in the visible light region is 420 nm to 780 nm is λ1, the value on the 20 nm lower wavelength side than λ1 is λ2, the value on the 20 nm higher wavelength side In the case of λ3, it means that the absorbance λ1 / λ2 or the absorbance λ1 / λ3 is 1.0 or more.

  The light absorber is not particularly limited as long as it absorbs light of a specific wavelength among light in a wavelength range of 350 nm to 780 nm, and, for example, quinoline dyes, anthraquinone dyes, perylene dyes and the like And one or more of these may be used in combination.

  As the quinoline dye, for example, 2-methylquinoline, 3-methylquinoline, 4-methylquinoline, 6-methylquinoline, 7-methylquinoline, 8-methylquinoline, 6-isopropylquinoline, 2,4-dimethylquinoline, Alkyl substituted quinoline compounds such as 2,6-dimethylquinoline and 4,6,8-trimethylquinoline, 2-aminoquinoline, 3-aminoquinoline, 5-aminoquinoline, 6-aminoquinoline, 8-aminoquinoline, 6-amino Amino-substituted quinoline compounds such as -2-methylquinoline, alkoxy-substituted quinoline compounds such as 6-methoxy-2-methylquinoline and 6,8-dimethoxy-4-methylquinoline, 6-chloroquinoline, 4,7-dichloro Halo such as quinoline, 3-bromoquinoline, 7-chloro-2-methylquinoline and the like Down-substituted quinoline compounds and the like.

  By blending such a quinoline dye, it is possible to absorb light having a wavelength range of 350 nm or more and 550 nm or less among light incident on the specific wavelength absorbing layer 11. In addition, it is preferable to have an absorption peak in a wavelength range of 400 nm or more and 550 nm or less.

  Examples of anthraquinone dyes include (1) 2-anilino-1,3,4-trifluoroanthraquinone, (2) 2- (o-ethoxycarbonylanilino) -1,3,4-trifluoroanthraquinone, 3) 2- (p-Ethoxycarbonylanilino) -1,3,4-trifluoroanthraquinone, (4) 2- (m-ethoxycarbonylanilino) -1,3,4-trifluoroanthraquinone, (5) 2- (o-cyanoanilino) -1,3,4-trifluoroanthraquinone, (6) 2- (p-cyanoanilino) -1,3,4-trifluoroanthraquinone, (7) 2- (m-cyanoanilino)- 1,3,4-Trifluoroanthraquinone, (8) 2- (o-nitroanilino) -1,3,4-trifluoroanthraquinone, (9) 2- (p) Nitroanilino) -1,3,4-trifluoroanthraquinone, (10) 2- (m-nitroanilino) -1,3,4-trifluoroanthraquinone, (11) 2- (p-tertiarybutylanilino) -1 , 3,4-trifluoroanthraquinone, (12) 2- (o-methoxyanilino) -1,3,4-trifluoroanthraquinone, (13) 2- (2,6-diisopropylanilino) -1,3 , 4-Trifluoroanthraquinone, (14) 2- (2,6-dichloroanilino) -1,3,4-trifluoroanthraquinone, (15) 2- (2,6-difluoroanilino) -1,3 , 4-Trifluoroanthraquinone, (16) 2- (3,4-dicyanoanilino) -1,3,4-trifluoroanthraquinone, (17) 2- (2,4,6-trithio) Loroanilino) -1,3,4-trifluoroanthraquinone, (18) 2- (2,3,5,6-tetrachloroanilino) -1,3,4-trifluoroanthraquinone, (19) 2- (2) (3,5,6-tetrafluoroanilino) -1,3,4-trifluoroanthraquinone, (20) 3- (2,3,4,5-tetrafluoroanilino) -2-butoxy-1,4 -Difluoroanthraquinone, (21) 3- (4-cyano-3-chloroanilino) -2-octyloxy-1,4-difluoroanthraquinone, (22) 3- (3,4-dicyanoanilino) -2-hexyloxy-1 , 4-Difluoroanthraquinone, (23) 3- (4-cyano-3-chloroanilino) -1,2-dibutoxy-4-fluoroanthraquinone, (24) 3- (p-cia) Noanilino) -2-phenoxy-1,4-difluoroanthraquinone, (25) 3- (p-cyanoanilino) -2- (2,6-diethylphenoxy) -1,4-difluoroanthraquinone, (26) 3- (2) , 6-Dichloroanilino) -2- (2,6-dichlorophenoxy) -1,4-difluoroanthraquinone, (27) 3- (2,3,5,6-tetrachloroanilino) -2- (2) , 6-Dimethoxyphenoxy) -1,4-difluoroanthraquinone, (28) 2,3-dianilino-1,4-difluoroanthraquinone, (29) 2,3-bis (p-tertiarybutylanilino) -1, 4-difluoroanthraquinone, (30) 2,3-bis (p-methoxyanilino) -1,4-difluoroanthraquinone, (31) 2,3-bis (2-methyl) Xyl-6-methylanilino) -1,4-difluoroanthraquinone, (32) 2,3-bis (2,6-diisopropylanilino) -1,4-difluoroanthraquinone, (33) 2,3-bis (2, 2, 3-bis (2, 6) 4,6-Trichloroanilino) -1,4-difluoroanthraquinone, (34) 2,3-bis (2,3,5,6-tetrachloroanilino) -1,4-difluoroanthraquinone, (35) 2 , 3-bis (2,3,5,6-tetrafluoroanilino) -1,4-difluoroanthraquinone, (36) 2,3-bis (p-cyanoanilino) -1-methoxyethoxy-4-fluoroanthraquinone, (37) 2- (2,6-dichloroanilino) -1,3,4-trichloroanthraquinone, (38) 2- (2,3,5,6-tetrafluoroanilino) 1,3,4-Trichloroanthraquinone, (39) 3- (2,6-dichloroanilino) -2- (2,6-dichlorophenoxy) -1,4-dichloroanthraquinone, (40) 2- (2, 6-dichloroanilino) anthraquinone, (41) 2- (2,3,5,6-tetrafluoroanilino) anthraquinone, (42) 3- (2,6-dichloroanilino) -2- (2,6) -Dichlorophenoxy) anthraquinone, (43) 2,3-bis (2-methoxy-6-methylanilino) -1,4-dichloroanthraquinone, (44) 2,3-bis (2,6-diisopropylanilino) anthraquinone, (45) 2-butylamino-1,3,4-trifluoroanthraquinone, (46) 1,4-bis (n-butylamino) -2,3-difluoroanthraquinone , (47) 1,4-bis (n-octylamino) -2,3-difluoroanthraquinone, (48) 1,4-bis (hydroxyethylamino) -2,3-difluoroanthraquinone, (49) 1,4 Bis (cyclohexylamino) -2,3-difluoroanthraquinone, (50) 1,4-bis (cyclohexylamino) -2-octyloxy-3-fluoroanthraquinone, (51) 1,2,4-tris (2 ,, 4-dimethoxyphenoxy-3-fluoroanthraquinone, (52) 2,3-bis (phenylthio) -1-phenoxy-4-fluoroanthraquinone, (53) 1,2,3,4-tetra (p-methoxyphenoxy)- Anthraquinone etc. are mentioned.

  By blending such an anthraquinone dye, it is possible to absorb light having a wavelength of 450 nm or more and 600 nm or less among light incident on the specific wavelength absorbing layer 11. In addition, it is preferable to have an absorption peak in a wavelength range of 500 nm to 600 nm.

  As a perylene pigment, for example, N, N'-dimethylperylene-3,4,9,10-tetracarboxylic acid diimide, N, N'-diethylperylene-3,4,9,10-tetracarboxylic acid diimide N, N'-bis (4-methoxyphenyl) -perylene-3,4,9,10-tetracarboxylic acid diimide, N, N'-bis (4-ethoxyphenyl) -perylene-3,4,9, 10-tetracarboxylic acid diimide, N, N'-bis (4-chlorophenyl) -perylene-3,4,9,10-tetracarboxylic acid diimide, etc. may be mentioned, with particular preference given to N, N'-bis Examples include (3,5-dimethylphenyl) -perylene-3,4,9,10-tetracarboxylic acid diimide and the like.

  By blending such a perylene-based dye, it is possible to absorb light having a wavelength of 400 nm or more and 800 nm or less among light incident on the specific wavelength absorbing layer 11. In addition, it is preferable to have an absorption peak in a wavelength range of 600 nm or more and 780 nm or less.

  By blending the light absorber as described above, it is possible to absorb light in a specific wavelength range. Thus, for example, the user can clearly recognize the contour of an object or a person in the wearing state, and can enhance the safety.

  The content of the light absorber (total of each light absorber) in the specific wavelength absorbing layer 11 is preferably 0.001 wt% or more and 5 wt% or less, and more preferably 0.003 wt% or more and 4 wt% or less preferable. Thereby, the above-mentioned effect can be exhibited more certainly. If the content is too small, the effect as a light absorber may not be obtained sufficiently. On the other hand, when the content is too large, the light absorber tends to be easily aggregated.

<UV absorber>
The ultraviolet absorber absorbs ultraviolet light (light in a wavelength range of 100 nm to 420 nm).

  The ultraviolet absorber is not particularly limited, and examples thereof include triazine compounds, benzophenone compounds, benzotriazole compounds and cyanoacrylate compounds, and one or more of these may be used in combination. Among these, triazine compounds are preferably used. Thereby, deterioration of the specific wavelength absorbing layer 11 (polycarbonate and light absorbing agent) due to ultraviolet light can be prevented or suppressed, and the weather resistance of the optical sheet 1 can be enhanced.

  As the triazine compounds, 2-mono (hydroxyphenyl) -1,3,5-triazine compounds, 2,4-bis (hydroxyphenyl) -1,3,5-triazine compounds, 2,4,6-tris ( And hydroxyphenyl) -1,3,5-triazine compounds. Specifically, 2,4-diphenyl-6- (2-hydroxy-4-methoxyphenyl) -1,3,5-triazine, 2, 4-diphenyl-6- (2-hydroxy-4-ethoxyphenyl) -1,3,5-triazine, 2,4-diphenyl- (2-hydroxy-4-propoxyphenyl) -1,3,5-triazine, 2,4-Diphenyl- (2-hydroxy-4-butoxyphenyl) -1,3,5-triazine, 2,4-diphenyl-6- (2-hydroxy-4-butoxyphenyl) -1,3,5-Triazine, 2,4-diphenyl-6- (2-hydroxy-4-hexyloxyphenyl) -1,3,5-triazine, 2,4-diphenyl-6- (2-hydroxy- 4-octyloxyphenyl) -1,3,5-triazine, 2,4-diphenyl-6- (2-hydroxy-4-dodecyloxyphenyl) -1,3,5-triazine, 2,4-diphenyl-6 -(2-hydroxy-4-benzyloxyphenyl) -1,3,5-triazine, 2,4-diphenyl-6- (2-hydroxy-4-butoxyethoxy) -1,3,5-triazine, 2, 4-Bis (2-hydroxy-4-butoxyphenyl) -6- (2,4-dibutoxyphenyl) -1,3-5-triazine, 2,4,6-tris (2-hydroxy-4-methoxy) Nyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-ethoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4) -Propoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-butoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy) -4-Hexyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-octyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-dodecyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-benzyloxyphenyl) -1,3,5-triazine, 2,4 , 6-tris ( 2-hydroxy-4-ethoxyethoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-butoxyethoxyphenyl) -1,3,5-triazine, 2,4,6-triazine 6-tris (2-hydroxy-4-propoxyethoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4-methoxycarbonylpropyloxyphenyl) -1,3,5- Triazine, 2,4,6-tris (2-hydroxy-4-ethoxycarbonylethyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-4- (1- (2) -Ethoxyhexyloxy) -1-oxopropan-2-yloxy) phenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methy) -4-methoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-ethoxyphenyl) -1,3,5-triazine, 2,4,6 -Tris (2-hydroxy-3-methyl-4-propoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-butoxyphenyl) -1,3 5,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-hexyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-) Methyl-4-octyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-dodecyloxyphenyl) -1,3,5-triazine, 2, 4,6-Tris 2-hydroxy-3-methyl-4-benzyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-ethoxyethoxyphenyl) -1,3, 5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-butoxyethoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl) -4-propoxyethoxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy-3-methyl-4-methoxycarbonylpropyloxyphenyl) -1,3,5-triazine, 2 , 4,6-tris (2-hydroxy-3-methyl-4-ethoxycarbonylethyloxyphenyl) -1,3,5-triazine, 2,4,6-tris (2-hydroxy) And s-3-methyl-4- (1- (2-ethoxyhexyloxy) -1-oxopropan-2-yloxy) phenyl) -1,3,5-triazine. Moreover, as a commercial item of a triazine type ultraviolet absorber, "tinuvin 1577", "tinuvin 460", "tinuvin 477" (made by BASF Japan), "Adekastab LA-F70" (made by ADEKA) etc. are mentioned, for example.

  When the specific wavelength absorbing layer 11 further includes the ultraviolet absorber absorbing light in the wavelength range of 100 nm to 420 nm as described above, the wavelength of the light incident on the specific wavelength absorbing layer 11 is 100 nm to 420 nm or less Light can be absorbed. Thereby, deterioration of the specific wavelength absorbing layer 11 (polycarbonate and light absorbing agent) due to ultraviolet light can be prevented or suppressed, and the weather resistance of the optical sheet 1 can be enhanced.

  The content of the ultraviolet light absorber in the specific wavelength absorbing layer 11 is preferably 0.05 wt% or more and 8 wt% or less, and more preferably 0.07 wt% or more and 6 wt% or less. Thereby, the above-mentioned effect can be exhibited more certainly. If the content is too small, the effect as a UV absorber may not be sufficiently obtained. On the other hand, when the content is too large, the ultraviolet absorber tends to be easily aggregated.

  Here, the content of the ultraviolet light absorber in the specific wavelength absorption layer 11 is larger than the content of the light absorber in the specific wavelength absorption layer 11. Thus, the optical sheet 1 can absorb light of a specific wavelength range of visible light and can absorb ultraviolet light. In particular, the light absorbing agent is relatively susceptible to deterioration by ultraviolet light, but this deterioration can be prevented. Further, since the content of the ultraviolet light absorber in the specific wavelength absorption layer 11 is larger than the content of the light absorber in the specific wavelength absorption layer 11, the light absorber is more reliably prevented from being deteriorated by ultraviolet light. be able to.

  The ratio A / B of the content A of the light absorber in the specific wavelength absorption layer 11 to the content B of the ultraviolet absorber in the specific wavelength absorption layer 11 is not less than 0.000125 and not more than 0.625. Preferably, it is more preferably 0.00015 or more and 0.4 or less. Thereby, the effects of the present invention can be obtained more significantly.

  The thickness of such a specific wavelength absorbing layer 11 is not particularly limited, but is preferably 0.05 mm or more and 1.5 mm or less, and more preferably 0.3 mm or more and 0.7 mm or less. As a result, the handleability can be enhanced, and it is possible to prevent the optical components as a whole from being unnecessarily thick.

  The specific wavelength absorbing layer 11 may be manufactured by stretching or may be manufactured without stretching, but the degree of stretching is preferably 10% or less. More preferably, it is 5% or less. As a result, it is possible to prevent or suppress the occurrence of color unevenness, unevenness of the light absorber, and unevenness of the ultraviolet absorber during stretching.

  When the melting point of polycarbonate is T1 and the melting point T2 of the light absorbing agent, it is preferable to satisfy T1 <T2. Thereby, when mixing the polycarbonate in a molten state and the light absorbing agent, it is possible to prevent the light absorbing agent from being deteriorated or discolored by heat.

  When the melting point of the polycarbonate is T1 and the melting point T3 of the ultraviolet absorber is T1, it is preferable to satisfy T1 <T3. Thereby, when mixing the polycarbonate in a molten state and the light absorber, it is possible to prevent the ultraviolet absorber from being deteriorated or discolored by heat.

  The melting point T1 of the polycarbonate is preferably 250 ° C. or more and 400 ° C. or less, and more preferably 270 ° C. or more and 350 ° C. or less.

  The melting point T2 of the light absorbing agent is preferably 300 ° C. or more and 400 ° C. or less, and more preferably 330 ° C. or more and 360 ° C. or less. The melting point T3 of the ultraviolet absorber is preferably 310 ° C. or more and 370 ° C. or less, and more preferably 340 ° C. or more and 360 ° C. or less.

  By setting the melting points T1 to T3 in the above numerical range, the above effect can be more reliably exhibited.

  The specific wavelength absorbing layer 11 may contain a pigment different from the pigment mentioned above. The dye is not particularly limited, and examples thereof include pigments, dyes and the like, and these can be used alone or in combination.

  The pigment is not particularly limited, and examples thereof include phthalocyanine pigments such as phthalocyanine green and phthalocyanine blue, fast yellow, disazo yellow, condensed azo yellow, benzoimidazolone yellow, dinitroaniline orange, penz imidazolone orange, toluidine red, Azo pigments such as permanent carmine, permanent red, naphthol red, condensed azo red, benzimidazolone carmine, benzimidazolone brown, anthraquinone pigments such as anthrapyrimidine yellow and anthraquinonil red, azomethine pigments such as copper azomethine yellow, Quinophthalone pigments such as quinophthalone yellow, isoindoline pigments such as isoindoline yellow, nitroso pigments such as nickel dioxime yellow Perinone pigments such as perinone orange, quinacridone magenta, quinacridone maroon, quinacridone scarlet, quinacridone red such as quinacridone red, perylene pigments such as perylene red and perylene maroon, pyrrolopyrrole pigments such as diketopyrrolopyrrole red, di Organic pigments such as dioxazine pigments such as oxazine violet, carbon pigments such as carbon black, lamp black, furnace black, ivory black, graphite and fullerene, chromate pigments such as yellow lead and molybdate orange, cadmium yellow , Cadmium Litopon Yellow, Cadmium Orange, Cadmium Litopon Orange, Ginkgo, Cadmium Red, Cadmium Litopon Red, sulfide-based pigments such as sulfurized, aker, titanium yellow, Tanbarium nickel yellow, red iron oxide, red lead, amber, brown iron oxide, zinc iron chromium brown, chromium oxide, cobalt green, cobalt chromium green, titanium cobalt green, cobalt blue, cerulian blue, cobalt aluminum chromium blue, iron black, manganese Oxide pigments such as ferrite black, cobalt ferrite black, copper chromium black and copper chromium manganese black, hydroxide pigments such as biridian, ferrocyanide pigments such as bitumen, silicate pigments such as ultramarine, cobalt And phosphate pigments such as violet and mineral violet, and other inorganic pigments such as cadmium sulfide and cadmium selenide, and the like, and one or more of them may be used in combination. .

  The dye is not particularly limited, and examples thereof include metal complex dyes, cyan dyes, xanthene dyes, azo dyes, hibiscus dyes, blackberry dyes, raspberry dyes, pomegranate juice dyes, chlorophyll dyes, tetraazoporphyrin compounds, etc. Porphyrin compounds and the like can be mentioned, and one or more of these can be used in combination.

  Next, a method of manufacturing an optical sheet and a method of manufacturing an optical component will be described. Below, the case where an optical sheet is manufactured using an extrusion method is demonstrated to an example.

(Method of manufacturing optical sheet)
First, an optical sheet manufacturing apparatus used in the present manufacturing method will be described.

  FIG. 3 is a side view schematically showing an optical sheet manufacturing apparatus for manufacturing the optical sheet shown in FIG. FIG. 4 is a cross-sectional view schematically showing an optical component manufacturing apparatus for manufacturing the optical sheet optical component shown in FIG. In the following description, the upper side in FIG. 4 is referred to as “upper” and the lower side as “lower”.

  The optical sheet manufacturing apparatus 100 shown in FIG. 3 includes a sheet supply unit 200 and a sheet forming unit 300.

  In the present embodiment, the sheet supply unit 200 includes an extruder 210 and a T-die 220 connected to the molten resin discharge unit of the extruder 210 through a pipe. The T-die 220 supplies the belt-shaped sheet 1 ′ in a molten or softened state to the sheet forming unit 300.

  The T-die 220 is an extrusion molding unit that extrudes the sheet 1 ′ in a molten or softened state into a band-like sheet by an extrusion method. The constituent materials constituting the optical sheet 1 described above are loaded in the molten state in the T-die 220, and the material in the molten state is pushed out from the T-die 220 to continuously deliver the strip-like sheet 1 '. Be

  The sheet forming unit 300 includes a touch roll 310, a cooling roll 320, and a post-stage cooling roll 330. Each of these rolls is configured to rotate independently by a motor (driving means) (not shown), and is continuously fed by being cooled by the rotation of these rolls. By continuously feeding the sheet 1 ′ to the sheet forming unit 300, the surface of the sheet 1 ′ is flattened, and the sheet 1 ′ is set to a desired thickness and cooled. And the optical sheet 1 is obtained by cut | disconnecting this cooled sheet | seat 1 'to predetermined length.

  The optical sheet of the present embodiment is manufactured by the method of manufacturing an optical sheet using the optical sheet manufacturing apparatus 100 as described above.

The production of an optical sheet includes an extrusion step, a molding step, and a cooling step.
First, the sheet 1 'in a molten or softened state in a band shape is extruded (extrusion step). In this extrusion process, the extruder 210 is loaded with the constituent materials of the optical sheet 1 (polycarbonate, light absorber, ultraviolet absorber, etc.). Further, the constituent material of the optical sheet 1 is in a melted or softened state in the extruder 210, and the polycarbonate, the light absorbing agent and the ultraviolet light absorbing agent are sufficiently mixed. And, by extruding these in the sufficiently mixed state, in the optical sheet 1 obtained through the forming step and the cooling step described later, excessive aggregation of the light absorbing agent and the ultraviolet light absorbing agent and the like is prevented can do.

  Next, the surface of the sheet 1 'is flattened, and the sheet 1' is set to a predetermined thickness (forming step). This process is performed between the touch roll 310 and the cooling roll 320.

  Next, the surface of the sheet 1 'is cooled (cooling step). This process is performed between the cooling roll 320 and the post-stage cooling roll 330.

  The optical sheet 1 can be obtained through the above steps. Next, a method of manufacturing an optical component will be described.

(Method of manufacturing optical parts)
First, an optical component manufacturing apparatus used in the present manufacturing method will be described.

  The optical component manufacturing apparatus 400 shown in FIG. 4 has a resin supply unit 500 and a mold 600. The resin supply unit 500 is filled with the polycarbonate described above. The mold 600 has a cavity 610 and a supply port 620 communicating the inside and the outside of the cavity 610. Further, the mold 600 is composed of the upper member 630 and the lower member 640, and in the assembled state where these are assembled, the mold 600 for defining the optical component manufacturing apparatus 400 is configured.

  The optical component manufacturing apparatus of the present embodiment is manufactured by the method of manufacturing an optical sheet manufacturing apparatus using the optical component manufacturing apparatus 400 as described above.

The optical component manufacturing method includes an optical sheet disposing step and a lens material supplying step.
First, in a state where the upper member 630 and the lower member 640 are disassembled, the optical sheet 1 is disposed on the bottom surface 641 of the lower member 640 (optical sheet disposing step). The bottom surface 641 is a curved concave surface, which allows the lens 4 to form a curved surface. Further, since the optical sheet 1 has flexibility, the optical sheet 1 is disposed following the shape of the bottom surface 641.

  Then, the upper member 630 and the lower member 640 are assembled, and the lens material in a molten or softened state is poured through the supply port 620 (lens material supply step). Then, by cooling the lens material in a molten or softened state, a laminate in which the optical sheet 1 and the lens are laminated can be obtained.

  In the above, the so-called sheet insert method has been described as an example, but the present invention is not limited to this, and for example, the optical sheet 1 is laminated to a molded lens via an adhesive. Good.

Second Embodiment
FIG. 6 is a cross-sectional view of an optical component provided with the optical sheet (second embodiment) of the present invention.

Hereinafter, the second embodiment of the optical sheet and the optical component of the present invention will be described with reference to this figure, but differences from the above-described embodiment will be mainly described, and the same matters will not be described.
This embodiment is the same as the first embodiment except that it has a polarizing film.

(Polarizing film)
As shown in FIG. 6, the optical sheet 1A further includes a polarizing film 12 and an adhesive layer 13. The polarizing film 12 is laminated on the specific wavelength absorbing layer 11 via the adhesive layer 13. In the illustrated configuration, the polarizing film 12 is disposed on the lens 4 side.

  The polarizing film 12 has a function of extracting linearly polarized light having a polarization plane in one predetermined direction from incident light (natural light which is not polarized). Thereby, the incident light entering the eye through the optical sheet 1 is polarized.

  Although the degree of polarization of the polarizing film 12 is not particularly limited, for example, it is preferably 50% or more and 100% or less, and more preferably 80% or more and 100% or less. The visible light transmittance of the polarizing film 12 is not particularly limited, but is preferably 10% to 80%, and more preferably 20% to 50%.

  The constituent material of such a polarizing film 12 is not particularly limited as long as it has the above-mentioned function, but, for example, polyvinyl alcohol (PVA), partially formalized polyvinyl alcohol, polyethylene vinyl alcohol, polyvinyl butyral, polycarbonate, ethylene- Those obtained by adsorbing, staining, and uniaxially stretching a dichroic substance such as iodine or a dichroic dye on a polymer film composed of a vinyl acetate copolymer partial saponifier or the like, a polyvinyl alcohol dehydration product or poly Examples include polyene-based oriented films such as dechlorinated products of vinyl chloride.

  Among these, it is preferable that the polarizing film 12 be uniaxially stretched by adsorbing iodine or a dichroic dye to a polymer film having polyvinyl alcohol (PVA) as a main material, and dye it. Polyvinyl alcohol (PVA) is a material excellent in all of transparency, heat resistance, affinity to iodine as a staining agent or dichroic dye, and orientation at the time of stretching. Therefore, the polarizing film 12 mainly composed of PVA is excellent in heat resistance and is excellent in polarizing function.

  Examples of the dichroic dye include chloratin fast red, congo red, brilliant blue 6B, benzoperpurine, chlorazole black BH, direct blue 2B, diamine green, chrysophenone, Sirius yellow, direct first red, acid black Etc.

  The thickness of the polarizing film 12 is not particularly limited, and is preferably, for example, 5 μm to 60 μm, and more preferably 10 μm to 40 μm.

  The adhesive (or pressure-sensitive adhesive) constituting the adhesive layer 13 is not particularly limited, and examples thereof include an acrylic adhesive, a urethane adhesive, an epoxy adhesive, a silicone adhesive, and the like.

  Among these, urethane adhesives are preferable. As a result, while the transparency, adhesive strength, and durability of the adhesive layer 13 are further improved, the followability to the shape change can be made particularly excellent.

  According to this embodiment as well, the same effect as that of the first embodiment can be obtained, and further, it has a polarization function.

  As mentioned above, although the suitable embodiment of the present invention was described, the present invention is not limited to what was mentioned above, A modification, improvement, etc. in the range which can achieve the object of the present invention are included in the present invention It is.

  For example, each part which comprises the optical sheet of this invention can be substituted by the thing of arbitrary structures which can exhibit the same function.

  In addition to the above-described configuration, the optical sheet of the present invention may have an optional component added.

  More specifically, for example, the optical sheet of the present invention may be provided with a protective layer for protecting the surface, an intermediate layer, a power adjustment layer for adjusting the power as a lens, and the like.

Hereinafter, the present invention will be more specifically described based on examples.
1. Examination of optical sheet 1-1. Create optical sheet

Example 1
[1] First, 100 parts by mass of bisphenol A type polycarbonate (Mitsubishi Gas Chemical Co., Ltd., "Iupilon E2000F E5111") and 0.04 parts by mass of a light absorber (manufactured by Yamada Chemical Industry Co., Ltd., "FDG-005") An optical sheet forming material was prepared by stirring and mixing 0.4 parts by mass of an ultraviolet absorber ("Adekastab LA-31G" manufactured by Adeka Co., Ltd.).

  [2] Next, the optical sheet forming material was stored in the extruder 210 of the optical sheet manufacturing apparatus 100 shown in FIG. 3 and melted, and extrusion molding was performed from the T-die 220 to obtain a sheet material. Then, the sheet material was cooled and formed by the sheet forming unit 300, and cut into a rectangular shape having an average thickness of 0.3 mm and 500 mm × 500 mm in plan view, to prepare an optical sheet.

  In addition, the viscosity average molecular weight Mv of polycarbonate is 27000, the melting point T1 is 250 ° C., and the melt flow rate measured in accordance with JIS K 7210 is 5.3 g / 10 min. The water absorption measured by Lavender Co., Ltd.) was 0.05%. Moreover, melting | fusing point T2 of the light absorber was 440 degreeC. Moreover, melting | fusing point T3 of the ultraviolet absorber was 200 degreeC.

Example 2
An optical sheet of Example 2 was obtained in the same manner as Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

[Example 3]
An optical sheet of Example 3 was obtained in the same manner as Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

Example 4
An optical sheet of Example 4 was obtained in the same manner as Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

[Example 5]
An optical sheet of Example 5 was obtained in the same manner as Example 1 except that the structure of the optical sheet was changed as shown in Table 1.

[Example 6]
An optical sheet of Example 6 was obtained in the same manner as Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

[Example 7]
An optical sheet of Example 7 was obtained in the same manner as in Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

Comparative Example 1
An optical sheet of Comparative Example 1 was obtained in the same manner as Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

Comparative Example 2
An optical sheet of Comparative Example 2 was obtained in the same manner as Example 1 except that the configuration of the optical sheet was changed as shown in Table 1.

  In Table 1, a1 represents polycarbonate (Mitsubishi Gas Chemical Co., Ltd., "E2000FN E5100"), a2 represents polycarbonate (Mitsubishi Gas Chemical Co., Ltd., "H3000"), and a3 represents polycarbonate (Sumiten) A4 shows polycarbonate (made by Mitsubishi Gas Chemical Co., Ltd., "S2000") and a5 shows polycarbonate (made by EG, "1300-03").

  Further, in Table 1, b1 represents a light absorbing agent (manufactured by Yamada Chemical Industry Co., Ltd., "FDG-005"), and in Table 1, b2 represents a light absorbing agent (manufactured by Yamada Chemical Industry Co., Ltd., "FDG-002") B) in Table 1 is a light absorber (manufactured by Yamada Chemical Industry Co., Ltd., "FDB-001").

  Further, in Table 1, c represents an ultraviolet absorber ("Adekastab LA-31G" manufactured by Adeka Co., Ltd.).

1-2. Evaluation The optical sheet of each example and each comparative example was evaluated by the following method.

(Cohesive evaluation)
The observation was performed using a digital microscope ("VHX-1000" manufactured by Keyence Corporation), the size of the aggregate was measured, and evaluated as follows.

A: Size of aggregate is less than 0.05 mm ² .
B: The size of the aggregate is 0.05 mm ² or more and less than 0.1 mm ² .
C: Size of aggregate is 0.1 mm ² or more and less than 0.5 mm ² .
D: The size of aggregates is 0.5 mm ² or more.

(Strength evaluation)
Charpy impact strength was measured in accordance with ISO 179-1 and ISO 179-2 and evaluated as follows.

A: 80 KJ / m ² or more.
B: 50 kJ / ^{m 2} or more 80 kJ / ^m less than ^2.
C: 25 kJ / ^{m 2} or more 50 kJ / ^m less than ^2.
D: less than 25 KJ / m ² .

(Weatherability evaluation)
Xenon lamp (7.5 kw, output: 1.728 MJ / m ² ) (light source filter: daylight filter, irradiance: broad band (300 to 400 nm), 60 ± 2 W / m ² ) irradiated for 8 hours, yellowing The degree (ΔYI) was evaluated as follows.

A: No change in appearance when ΔYI is less than 1.0.
B: A slight change in appearance is observed when ΔYI is 1.0 or more and less than 2.0.
C: A change in appearance is observed when ΔYI is 2.0 or more and less than 3.0.
D: A remarkable change in appearance is observed when ΔYI is 3.0 or more.

  The evaluation results of the optical sheets of Examples and Comparative Examples obtained as described above are shown in Table 1 below.

  As shown in Table 1, the optical sheets in the respective examples resulted in excellent strength and weather resistance equal to or higher than those of the respective comparative examples.

2. Examination of weatherability of light absorber itself 2-1. Preparation of Optical Sheet [Example A]
[1] First, 100 parts by mass of an acrylic resin (Sumipex MG5 manufactured by Sumitomo Chemical Co., Ltd.), and 0.04 parts by mass of a light absorber (manufactured by Yamada Chemical Industry Co., Ltd., "FDG-005"), 0.4 mass An optical sheet forming material was prepared by stirring and mixing an ultraviolet absorber ("Adekastab LA-31G" manufactured by Adeka Co., Ltd.) in a part.

  [2] Next, the optical sheet forming material was stored in the extruder 210 of the optical sheet manufacturing apparatus 100 shown in FIG. 3 and melted, and extrusion molding was performed from the T-die 220 to obtain a sheet material. Then, the sheet material was cooled and formed by the sheet forming unit 300, and cut into a rectangular shape having an average thickness of 0.3 mm and 500 mm × 500 mm in plan view, to prepare an optical sheet.

Example B
An optical sheet of Example B was obtained in the same manner as Example A except that the configuration of the optical sheet was changed as shown in Table 2.

Example C
An optical sheet of Example C was obtained in the same manner as Example A except that the configuration of the optical sheet was changed as shown in Table 2.

Example D
An optical sheet of Example D was obtained in the same manner as Example A except that the configuration of the optical sheet was changed as shown in Table 2.

Example E
An optical sheet of Example E was obtained in the same manner as Example A except that the configuration of the optical sheet was changed as shown in Table 2.

Comparative Example A
An optical sheet of Comparative Example A was obtained in the same manner as Example A except that the configuration of the optical sheet was changed as shown in Table 2.

  Further, in Table 2, b1 represents a light absorbing agent (manufactured by Yamada Chemical Industry Co., Ltd., "FDG-005"), and in Table 1, b2 represents a light absorbing agent (manufactured by Yamada Chemical Industry Co., Ltd., "FDG-002") ) Is shown.

  Moreover, in Table 2, c has shown the ultraviolet absorber (The Adeka company make, "Adekastab LA-31G").

2-2. Evaluation The optical sheet of each example and comparative example was evaluated by the following method.

(Weatherability evaluation of light absorbers)
Each optical sheet is irradiated with ultraviolet light for 48 hours at an irradiation dose of 150 mW / cm ² using a UV tester (SUV-W161 manufactured by Iwasaki Electric Co., Ltd.), and then the peak top of the light absorbing agent is transmitted by a spectrophotometer The difference between the peak top transmittance of the light absorber before the test and the transmittance of the peak top of the light absorber after the test was calculated and evaluated as follows.

A: Difference in transmittance is less than 3% B: Difference in transmittance is 3% to less than 5% C: Difference in transmittance is 5% to less than 10% D: Difference in transmittance is 10% or more

  The evaluation results of the optical sheets of the examples and comparative examples obtained as described above are shown in Table 2 below.

  As shown in Table 2, in the optical sheet in each example, the result was excellent in the weather resistance more than the comparative example. In addition, although it replaced with the polycarbonate and evaluated above using acrylic resin ("Sumipex MG5" by Sumitomo Chemical Co., Ltd.), it is because the weather resistance evaluation of a light absorber is performed more notably, Comprising: A polycarbonate is used It is known that the same tendency can be obtained.

DESCRIPTION OF SYMBOLS 1 optical sheet 1 'sheet 1A optical sheet 2 frame 3 lens with lens 4 lens 5 mounting part 6 flange 7 light transmissive member 10 optical component 10' optical component 11 specific wavelength absorption layer 12 polarizing film 13 adhesive layer 21 rim portion 22 Bridge part 23 Temple part 24 Nose pad part 100 Optical sheet manufacturing device 200 Sheet supply part 210 Extruder 211 Molten resin discharge part 212 Piping 220 T die 300 Sheet forming part 310 Touch roll 320 Cooling roll 330 Post-stage cooling roll 400 Optical parts manufacture Device 500 Resin supply unit 600 Mold 610 Cavity 620 Supply port 630 Upper member 640 Lower member 641 Bottom surface

Claims (5)

Wavelength of 350 nm or more and 740 nm or less with a polycarbonate having a viscosity average molecular weight Mv of 24000 or more and 27500 or less and a melt flow rate measured according to JIS K 7210 of 5.3 g / 10 min or more and 25 g / 10 min or less A specific wavelength absorbing layer including a light absorbing agent that absorbs light of a specific wavelength and an ultraviolet light absorbing agent that absorbs light having a wavelength of 100 nm or more and 420 nm or less among light in the range ;
The melting point of the light absorber is 300 ° C. or more and 400 ° C. or less,
The content of the light absorbing agent before Symbol specific wavelength absorbing layer is less than 0.003 wt% 4 wt%,
The content of the ultraviolet light absorber in the specific wavelength absorption layer is greater than the content of the light absorber in the specific wavelength absorption layer, and is 0.07 wt% or more and 6 wt% or less. Sheet.   The optical sheet according to claim 1, wherein the polycarbonate has a water absorption of 0.02% or more and 0.2% or less.   The optical sheet according to claim 1 or 2, wherein the melting point T1 of the polycarbonate is smaller than the melting point T2 of the light absorber and the melting point T3 of the ultraviolet absorber.   The optical sheet according to any one of claims 1 to 3, wherein the specific wavelength absorbing layer has a degree of stretching of 10% or less. A substrate,
An optical component comprising: the optical sheet according to any one of claims 1 to 4 laminated on the base material.

Images