JP6332268B2 - Glass laminate - Google Patents

Description

  The present invention relates to a glass laminate in which a resin layer is laminated on a thin film glass via an adhesive.

  In recent years, the size of display devices has been increasing, and mobile devices have also been increasing. Thus, thin and light display devices are required. A glass substrate is generally used for the display device, and the display device can be made thin and light by thinning the glass substrate. However, when the glass substrate is thinned, the glass substrate is easily broken and the handling property is deteriorated. As a countermeasure, a method has been proposed in which thin film glass and a film are bonded together to compensate for the flexibility and cracking property of the thin film glass.

  For example, in patent document 1, the reduction | damage at the time of handling a glass film is aimed at by adhere | attaching a resin film on the glass film of thickness 0.1 micrometer-100 micrometers via an acrylic adhesive.

JP 2001-97733 A (see claim 1, paragraphs [0017], [0059], etc.)

  By the way, since the display device is used for various uses such as a mobile use, an in-vehicle use, and a digital signage use, it may be placed in various environments. Therefore, when a laminated body of thin glass and a film (resin layer) (hereinafter sometimes referred to as a glass laminated body) is used as a member of a display device (for example, an organic EL gas barrier layer), severe heat shock test resistance is obtained. Required. Then, when it applied to the heat shock test using the glass laminated body which bonded the thin film glass and the film with the common acrylic adhesive, the problem that a film and thin film glass peeled generate | occur | produced.

  In view of the above circumstances, an object of the present invention is to provide a glass laminate having heat shock test resistance and good handling properties even when the resin layer is laminated on the thin film glass via an adhesive. There is to do.

  The above object of the present invention is achieved by the following configurations.

1. The thin film glass and the first resin layer are bonded with the first adhesive,
The first adhesive includes a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound,
The glass laminate is characterized in that the first resin layer has a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH as measured in accordance with JIS Z 0208.

  2. 2. The glass laminate according to 1 above, wherein the first resin layer contains a cellulose derivative.

  3. 3. The glass laminate according to 1 or 2, wherein the hydroxyl group-containing polymer compound contained in the first adhesive contains a cellulose derivative.

  4). 4. The glass laminate as described in 3 above, wherein the cellulose derivative contained in the first adhesive is a cellulose ester.

  5. The reactive metal compound contained in a 1st adhesive agent is a metal alkoxide, The glass laminated body in any one of said 1-4 characterized by the above-mentioned.

6). A second resin layer is bonded with a second adhesive on the side opposite to the side on which the first resin layer of the thin film glass is laminated,
6. The glass laminate according to any one of 1 to 5, wherein the second adhesive contains a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound.

  7). The glass laminate as described in 6 above, wherein the second resin layer contains a cellulose derivative.

  8). 8. The glass laminate as described in 6 or 7 above, wherein the hydroxyl group-containing polymer compound contained in the second adhesive contains a cellulose derivative.

  9. 9. The glass laminate as described in 8 above, wherein the cellulose derivative contained in the second adhesive is a cellulose ester.

  10. 10. The glass laminate according to any one of 6 to 9, wherein the reactive metal compound contained in the second adhesive is a metal alkoxide.

  11. 11. The glass laminate according to any one of 1 to 10, wherein the thin film glass has a thickness of 5 to 100 μm.

  The metal component contained in the reactive metal compound can be covalently bonded to the glass component. On the other hand, the hydroxyl group-containing polymer compound contains a hydroxyl group and has high affinity with the resin. For this reason, the 1st adhesive agent which adhere | attaches thin film glass and a 1st resin layer is a cocondensate of a reactive metal compound and a hydroxyl-containing polymer compound, and the characteristic of a reactive metal compound, and hydroxyl-containing high By having both the characteristics of the molecular compound, it is possible to ensure good adhesion to both the thin film glass and the first resin layer. And the adhesiveness of thin film glass and a 1st resin layer can be improved through a 1st adhesive agent.

  In addition, by using a highly moisture permeable film as the first resin layer, alcohol generated when the first adhesive is applied can be quickly released, and no reverse reaction occurs even in the heat shock test. Adhesion can be maintained after the shock test. Therefore, when this glass laminate is used for a display device, it can be used for various purposes and can be used without any problem for a long time even when placed in various environments.

  Moreover, since the glass laminated body has laminated | stacked the 1st resin layer on thin film glass, handling property becomes favorable and it becomes difficult to break at the time of handling.

It is sectional drawing which shows the schematic structure of the organic electroluminescence display to which the glass laminated body which concerns on embodiment of this invention is applied. It is sectional drawing which shows the example of a structure different from what was shown in FIG. 1 of the polarizing plate used for the said organic EL display apparatus. It is sectional drawing which shows the structural example different from what was shown in FIG. 1 of the said glass laminated body. It is sectional drawing which shows the schematic structure of the liquid crystal display device to which the said glass laminated body is applied.

  An embodiment of the present invention will be described below with reference to the drawings. In the present specification, when the numerical range is expressed as A to B, the numerical value range includes the values of the lower limit A and the upper limit B.

[Configuration of organic EL display device]
FIG. 1 is a cross-sectional view showing a schematic configuration of an organic EL display device 1 of the present embodiment. The organic EL display device 1 is configured by laminating an organic EL element 2, a glass laminate 3, and a polarizing plate 4 in this order. In the figure, the organic EL element 2, the glass laminate 3, and the polarizing plate 4 are shown separated from each other for the purpose of clearly distinguishing them.

  The organic EL element 2 is a display called OLED (Organic light-Emitting Diode), and in order on a substrate 21 made of glass, polyimide, or the like, for example, a metal electrode 22 made of aluminum, a light emitting layer 23 and a transparent electrode ( For example, an ITO (Indium Tin Oxide) 24 is included. In addition, originally, sealing glass for surface protection is provided on the transparent electrode 24, but in this embodiment, the glass laminate 3 bonded with the polarizing plate 4 is used instead of this sealing glass. ing.

  When a voltage is applied to the metal electrode 22 and the transparent electrode 24, electrons are injected from the electrode serving as the cathode among the metal electrode 22 and the transparent electrode 24 into the light emitting layer 23, and holes are injected from the electrode serving as the anode. Then, when the two recombine at the light emitting layer 23, visible light emission corresponding to the light emission characteristics of the light emitting layer 23 occurs. The light generated in the light emitting layer 23 is taken out to the outside directly or after being reflected by the metal electrode 22 through the transparent electrode 24 and the glass laminate 3.

  In the present embodiment, the glass laminate 3 has a function of imparting an in-plane retardation of about ¼ of the wavelength λ (nm) to the transmitted light, and the detailed configuration thereof will be described later. In the present invention, the glass laminate is not particularly limited as long as it is optically transparent.

  The polarizing plate 4 transmits predetermined linearly polarized light, and is configured by laminating a polarizing layer 41 (polarizer) and a protective layer 42. The polarizing layer 41 is obtained, for example, by dyeing a polyvinyl alcohol film with a dichroic dye and stretching the film at a high magnification. The thickness of the polarizing layer 41 is, for example, 10 μm or less. The protective layer 42 is composed of, for example, a cellulose resin or a hard coat layer, and is provided for the purpose of protecting the surface of the polarizing layer 41. The protective layer 42 is bonded to the polarizing layer 41 via an ultraviolet curable adhesive, or is bonded to the polarizing layer 41 using a polyvinyl alcohol aqueous solution as an adhesive (water glue).

  In FIG. 1, the protective layer 42 is formed only on one side of the polarizing layer 41 to constitute the polarizing plate 4. However, as shown in FIG. 2, the polarizing layer 41 is sandwiched between the protective layers 42 and 42 from both sides. The polarizing plate 4 may be configured as follows.

  As described above, by disposing the glass laminate 3 and the polarizing plate 4 on the external light incident side of the organic EL element 2, these are circular polarizing plates that prevent reflection of external light incident on the organic EL element 2. Function as. That is, of the external light incident on the polarizing plate 4, the light (linearly polarized light) transmitted through the polarizing layer 41 is converted into circularly polarized light by the glass laminate 3 and reflected by the metal electrode 22 of the organic EL element 2. The phase is inverted by 180 ° and reflected as circularly polarized light in the reverse direction. This reflected light again enters the glass laminate 3, is converted into linearly polarized light perpendicular to the transmission axis of the polarizing layer 41, and is all absorbed by the polarizing layer 41.

[Details of glass laminate]
Next, the detail of the above-mentioned glass laminated body 3 is demonstrated. As shown in FIG. 1, the glass laminate 3 has an adhesive layer 32 (first adhesive) and a λ / 4 retardation layer 33 (first resin layer) on one surface side of the thin film glass 31. The layers are laminated in this order, and an adhesive layer 34 (second adhesive) and a resin layer 35 (second resin layer) are laminated in this order on the other surface side. In the present embodiment, the glass laminate 3 is arranged such that the λ / 4 retardation layer 33 is located on the opposite side of the thin film glass 31 from the organic EL element 2, and the λ / 4 retardation layer 33. The polarizing layer 41 is bonded to the above. The glass laminate 3 may have a configuration in which the adhesive layer 34 and the resin layer 35 are omitted. That is, as shown in FIG. 3, even if the adhesive layer 32 and the λ / 4 retardation layer 33 are laminated on one surface side of the thin film glass 31, and the resin layer is not provided on the other surface side. Good.

  The case where the adhesive layers 32 and 34 are not clearly present as layers is also included in the scope of the present invention. It is assumed that the components contained in the adhesive layer are integrated by penetrating and reacting with the λ / 4 retardation layer 33 or the polarizing layer 41.

  The λ / 4 retardation layer 33 is a layer that imparts an in-plane retardation of about ¼ of the wavelength to the transmitted light. The angle formed between the slow axis of the λ / 4 retardation layer 33 and the absorption axis of the polarizing layer 41 is set to 30 to 60 °. Thereby, it becomes possible to switch the polarization state of incident light between linearly polarized light and circularly polarized light (or elliptically polarized light) by the combination of the λ / 4 retardation layer 33 and the polarizing layer 41.

  In addition, since the polarizing layer 41 is directly bonded to the λ / 4 retardation layer 33, both the polarizing layer 41 and the λ / 4 retardation layer 33 are similarly affected by the environmental variation (for example, temperature change). For this reason, there is almost no so-called axial deviation in which the direction of the slow axis of the λ / 4 retardation layer 33 and the direction of the absorption axis of the polarizing layer 41 are shifted due to environmental fluctuations.

  The λ / 4 retardation layer 33 includes a cellulose resin (cellulose derivative) or a polycarbonate resin (PC). From the viewpoint of heat resistance during a durability test, the cellulose resin (cellulose) having heat resistance is used. Derivatives) are desirable. As such a cellulose resin, for example, diacetyl cellulose (DAC) or cellulose acetate propionate (CAP) can be used.

  The adhesive layer 32 that bonds the thin film glass 31 and the λ / 4 retardation layer 33 includes a cocondensate of a reactive metal compound (inorganic compound) and a hydroxyl group-containing polymer compound (organic compound). It is an organic-inorganic hybrid adhesive layer (HB glue). The co-condensate of a reactive metal compound and a hydroxyl group-containing polymer compound means that it includes a structure in which a hydroxyl group generated from the reactive metal compound and a hydroxyl group in the hydroxyl group-containing polymer compound are subjected to a condensation reaction. As the reactive metal compound, for example, silicon alkoxide such as tetraethoxysilane (TEOS) or tetramethoxysilane (TMOS) can be used. As the hydroxyl group-containing polymer compound, for example, diacetyl cellulose (DAC) or cellulose acetate propionate (CAP) can be used. Details of the reactive metal compound and the hydroxyl group-containing polymer compound will be described later.

  The metal component contained in the reactive metal compound tends to be strongly bonded to the material component of the glass by a chemical bond such as a covalent bond. Moreover, since the hydroxyl group-containing polymer compound contains a hydroxyl group, it has high affinity with the resin and can improve adhesiveness. Therefore, by using the organic-inorganic hybrid type adhesive layer 32, the adhesion between the thin film glass 31 and the λ / 4 retardation layer 33 can be improved through the adhesive layer 32. Thereby, the dimensional change (resin expansion and contraction) of the λ / 4 retardation layer 33 due to the environmental change (temperature change, humidity change) during the durability test can be suppressed, and the slow axis of the λ / 4 retardation layer 33 can be suppressed. It is possible to prevent the direction from deviating from a predetermined direction. As a result, the occurrence of unevenness in the phase difference imparted to the transmitted light by the λ / 4 retardation layer 33 can be suppressed. In general, an organic compound and an inorganic compound are poorly compatible, but by forming these condensates, an adhesive layer 32 having both characteristics in a single layer structure can be easily realized. be able to.

  The resin layer 35 is laminated with an adhesive layer 34 on the side opposite to the λ / 4 retardation layer 33 with respect to the thin film glass 31 for the purpose of further improving the strength of the glass laminate 3. That is, by providing the resin layer 35, the thin film glass 31 is sandwiched between the resin layers (λ / 4 retardation layer 33, resin layer 35) from both sides. Compared with the configuration in which the phase difference layer 33) is provided, the strength of the entire glass laminate 3 can be further improved. As a result, the handling properties of the glass laminate 3 are improved and are less likely to be damaged during handling.

  Here, when the light emitting layer 23 of the organic EL element 2 described above is configured to emit white light, for example, R (red), G (green), and B (blue) in order to support color display. Color filters are required. In this case, for example, there is a method of forming a color filter on the resin layer 35 side of the glass laminate 3 by an ink jet method using a latent pigment as ink. In this method, heating is required for fixing the latent pigment. Therefore, from the viewpoint of heat resistance against heating, it is desirable to use a cellulose resin having heat resistance such as triacetyl cellulose (TAC) as the resin layer 35.

  In addition, when the light emitting layer 23 is comprised so that each light of RGB may be light-emitted, since the heat resistance at the time of the above-mentioned color filter formation is unnecessary for the resin layer 35, the resin layer 35 other than a cellulose resin is used. Resin (for example, polycarbonate resin) can be used.

  In the case of an organic EL display device that does not have the polarizing plate 4, the glass laminate 3 can use a resin layer 35 having no retardation function instead of the λ / 4 retardation layer 33. Similar to the λ / 4 retardation layer 33, the resin layer 35 includes a cellulose resin (cellulose derivative) or a polycarbonate resin (PC). From the viewpoint of heat resistance during the durability test, the resin layer 35 is heat resistant. It is desirable to contain a cellulose resin (cellulose derivative) having As such a cellulose resin, for example, diacetyl cellulose (DAC) or cellulose acetate propionate (CAP) can be used.

  The adhesive layer 34 that bonds the thin film glass 31 and the resin layer 35 may be made of any material as long as the thin film glass 31 and the resin layer 35 can be bonded. For example, a known acrylic pressure-sensitive adhesive (for example, PSA (Pressure Sensitive Adhesive, pressure-sensitive adhesive) or thermosetting epoxy resin can be used, but in the present embodiment, an organic-inorganic hybrid type adhesive layer similar to the adhesive layer 32 is used. It is configured.

  As described above, the metal component contained in the reactive metal compound is likely to be firmly bonded to the glass material component, and the hydroxyl group-containing polymer compound has a high affinity with the resin, so that the thin film glass 31 and the resin layer 35 are bonded. By using an organic-inorganic hybrid adhesive layer similar to the adhesive layer 32 as the layer 34, the adhesion between the thin film glass 31 and the resin layer 35 can be improved. Thereby, it can suppress that the resin layer 35 deteriorates with the heat | fever from the organic EL element 2 at the time of use, and the optical characteristic (for example, phase difference (retardation)) fluctuates.

  The hydroxyl group-containing polymer compound is desirably a cellulose ester (for example, DAC or CAP) having a total acyl group substitution degree of 1.0 to 2.6. Such a cellulose ester contains a hydroxyl group and improves the affinity with the λ / 4 retardation layer 33 or the resin layer 35 made of a resin. Therefore, the adhesion between the thin film glass 31 and the λ / 4 retardation layer 33 is improved. Alternatively, it is very effective as a material for improving the adhesion between the thin film glass 31 and the resin layer 35.

  Here, when HB glue used as the adhesive layers 32 and 34 undergoes hydrolysis of alkoxy groups or condensation reaction between alkoxy groups and hydroxyl groups, alcohol is generated in the adhesive layers. At this time, if the moisture permeability of the λ / 4 retardation layer 33 and the resin layer 35 is low, a large amount of alcohol remains in the adhesive layers 32 and 34. When subjected to the heat shock test in this state, a reverse reaction occurs due to the heated alcohol, the condensation is dissolved and the adhesive strength is reduced, and the thin film glass 31 and the λ / 4 retardation layer 33 or the resin layer 35 are peeled off. Therefore, by using a highly moisture permeable film for the λ / 4 retardation layer 33 and the resin layer 35, alcohol generated from the HB paste can be quickly released, no reverse reaction occurs, and the adhesive strength is maintained even after the heat shock test. I guess you can maintain.

Therefore, as the λ / 4 retardation layer 33 and the resin layer 35, a highly moisture permeable film having a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH measured in accordance with JIS Z 0208. Is used. The test result which led to this moisture permeability will be described later.

  In addition, the λ / 4 retardation layer 33 and the resin layer 35 are desirably 5 μm or more in thickness from the viewpoint of reinforcing the thin film glass 31.

  According to the configuration of the glass laminate 3 described above, since it has heat shock test resistance, the organic EL display device 1 provided with the glass laminate 3 on the organic EL element 2 is used for various purposes, and variously. Even when placed in the environment, it can be used for a long time without problems. Moreover, since the handleability of the glass laminated body 3 is favorable, productivity is good.

[Configuration of liquid crystal display device]
FIG. 4 is a cross-sectional view showing a schematic configuration of the liquid crystal display device 51 of the present embodiment. The glass laminate 3 described above can also be applied to the liquid crystal display device 51.

  The liquid crystal display device 51 includes a liquid crystal panel 52 and a backlight 53 that illuminates the liquid crystal panel 52. The liquid crystal panel 52 is configured by sandwiching a liquid crystal layer 63 between two substrates 61 and 62. The liquid crystal layer 63 is sealed between the two substrates 61 and 62 by a sealing material 64. A polarizing plate (not shown) is disposed in a crossed Nicols state on the outside of the substrates 61 and 62 (on the side opposite to the liquid crystal layer 63).

  The two substrates 61 and 62 are each composed of the glass laminate 3 described above. At this time, in order to suppress the dimensional change of the λ / 4 retardation layer 33 due to heat generated at the time of use (for example, heat generated at the electrode of the liquid crystal cell), the glass laminate 3 has the λ / 4 retardation layer 33 formed of a thin film glass. The liquid crystal layer 63 is disposed on the side opposite to the liquid crystal layer 63. In the substrates 61 and 62, the slow axes of the λ / 4 retardation layer 33 are perpendicular to each other, and the transmission axes of the two outer polarizing plates are also perpendicular to each other.

  On the liquid crystal layer 63 side of the substrate 62, a pixel electrode corresponding to each pixel, a TFT (Thin Film Transistor) which is a switching element for controlling ON / OFF of display in each pixel, and various types of TFTs connected to the TFT Wiring (including scanning lines and signal lines) and an alignment film for aligning liquid crystal molecules are formed. A common electrode, a color filter for performing color display, and an alignment film are formed on the liquid crystal layer 63 side of the substrate 61.

  In the above configuration, of the light emitted from the backlight 53, the light (linearly polarized light) transmitted through the polarizing plate outside the substrate 62 enters the liquid crystal layer 63 through the substrate 62, and the thickness of the liquid crystal layer 63 is increased. While propagating in the direction, the polarization state changes according to the refractive index anisotropy (birefringence) of the liquid crystal. Of the light incident on the substrate 61 via the liquid crystal layer 63, only the light of the polarization component in a specific direction passes through the polarizing plate outside the substrate 61 and is emitted to the viewer side as display light. Accordingly, an image can be displayed by changing the orientation of the liquid crystal molecules by changing the voltage applied to the liquid crystal layer 63 for each pixel by ON / OFF control of the TFT.

  In addition, by positioning the λ / 4 retardation layer 33 so as to sandwich the liquid crystal layer 63, luminance reduction due to the presence of a liquid crystal disclination portion (a portion where the liquid crystal alignment is discontinuous) is improved. However, by using the glass laminate 3, it is possible to suppress the occurrence of phase difference unevenness due to environmental fluctuations during the durability test, so the above-described reduction in luminance can be made uniform over the entire screen regardless of environmental fluctuations. Can be planned.

  Such an effect is obtained even when only one of the two substrates 61 and 62 is formed of the glass laminate 3 (the other substrate is made of a λ / 4 retardation layer and a glass by a conventional adhesive such as PSA). Even if the substrates 61 and 62 are made of the glass laminate 3, the effect can be maximized.

  Even when the glass laminate 3 is applied to the liquid crystal display device 51 as described above, the λ / 4 retardation layer 33 of the glass laminate 3 may be composed of a cellulose resin having heat resistance such as TAC. desirable. This is because, when a color filter is formed on the substrate 61 (glass laminate 3) by an inkjet method using a latent pigment, heat resistance against heating at the time of fixing the latent pigment is required.

  In a so-called COA (Color filter On Array) type liquid crystal display device in which a color filter is formed on the substrate 62 side where the TFT is formed, the λ / 4 retardation layer 33 of the glass laminate 3 used as the substrate 61. Since the heat resistance at the time of forming the color filter is unnecessary, the λ / 4 retardation layer 33 can be made of a resin other than the cellulose resin.

  The glass laminate 3 of the present embodiment includes TN (Twisted Nematic), IPS (In-Plane Switching), FLC (Ferroelectric Liquid Crystal), AFLC (Anti-ferroelectric Liquid Crystal), OCB (Optically Compensatory Bend), STN (Supper). It can be used as a cell substrate of a liquid crystal display device of various display modes such as Twisted Nematic (VA), VA (Vertical Alignment), and HAN (Hybrid Aligned Nematic).

  Among them, the IPS method has a feature that the viewing angle performance is superior to the TN method and the VA method. Therefore, when the glass laminate 3 (with the resin layer 35) of the present embodiment is used as the cell substrate of the IPS method. It is desirable that the phase difference in the resin layer 35 is almost zero (the visibility is improved when the phase difference is close to zero). From this, it is desirable that the in-plane retardation Ro of the resin layer 35 is 0 to 5 nm, and the thickness direction retardation Rt is −10 to 10 nm.

In addition, when the glass laminate 3 is applied to the liquid crystal display device 51 as described above, the liquid crystal display device 51 is used for various purposes such as mobile use, in-vehicle use, and digital signage use. Could be placed. Therefore, heat shock test resistance is required. Therefore, in the same manner as above, the λ / 4 retardation layer 33 and the resin layer 35 have a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH as measured in accordance with JIS Z 0208. A high moisture-permeable film is used. Thereby, the alcohol generated from the HB paste can be quickly released, no reverse reaction occurs, and the adhesive force can be maintained even after the heat shock test.

[Details of each layer]
Hereinafter, the detail of each layer which comprises a glass laminated body is demonstrated.

(Thin glass)
As thin film glass which comprises a glass laminated body, what was shape | molded by various shaping | molding methods can be used. For example, a thin film glass formed by a rollout method, a redraw method, a downdraw method, a float method, a fusion method or the like can be used.

  The shape of the thin film glass is not particularly limited and may be a chip cut shape, but is preferably a roll shape from the viewpoint of suitability for production on a roll-to-roll basis.

  The average thickness of the thin film glass is preferably 5 to 200 μm, and more preferably 5 to 100 μm. If the thickness is less than 5 μm, handling such as conveyance is difficult, and if the thickness exceeds 200 μm, the value of the thin film is diminished.

  The thin film glass is not particularly limited as long as it is a multicomponent oxide glass. For example, alkali-free glass, borosilicate glass, aluminosilicate glass and the like are particularly suitable as the thin film glass, and among them, alkali-free glass is most preferred.

  The surface of the thin film glass is preferably cleaned appropriately. If organic substances such as sebum and dust are attached, the adhesiveness with the adhesive layer is lowered. The cleaning method follows a known glass cleaning method. For example, alkali cleaning, acid cleaning, detergent cleaning, solvent cleaning, liquid jet cleaning, UV cleaning, excimer cleaning, plasma cleaning, ion cleaning, sputter cleaning, heat cleaning, dry ice jet Cleaning or the like is suitable as a cleaning method, and alkali cleaning, UV cleaning, and excimer cleaning are particularly preferable.

  Moreover, surface treatment may be performed in advance on the thin film glass. For example, it is preferably treated with a silicon alkoxide such as TEOS or TMOS, or a silane coupling agent.

(Polarizing layer)
The polarizing layer is an element (polarizer) that passes only light having a plane of polarization in a certain direction. As a typical element currently used as a polarizing layer, there is a polarizer using a polyvinyl alcohol-based resin, which includes a polyvinyl alcohol-based resin dyed with iodine and a dichroic dye. There is something.

  As a polarizer, a polyvinyl alcohol aqueous solution is formed into a film, and this is uniaxially stretched and dyed as a raw fabric, or is uniaxially stretched after being dyed, and preferably subjected to a durability treatment with a boron compound. Can be used. A thin film polarizer can be obtained by reducing the thickness of the original film.

  In addition, a coating-type thin film polarizer obtained by stretching, dyeing, and crosslinking a laminate obtained by coating and drying a polyvinyl alcohol aqueous solution on a stretching film substrate can also be used. For example, Japanese Patent Nos. 4279944, 2009-93074, No. 4691205, No. 4751481, No. 4804588, No. 4804589, No. 1701555, No. 2011-248293, etc. A coating-type thin film polarizer can be obtained with reference to FIG.

  After transferring the polarizer produced on the stretching film substrate onto the λ / 4 retardation layer, the stretching film substrate may be peeled off, or may be used as it is as a protective layer without peeling. Good. A coating-type thin film polarizer is preferably used because it can be made thinner than a polarizer using an original film.

  Further, a protective layer may be separately formed on the surface of the polarizing layer opposite to the adhesion side with the λ / 4 retardation layer. The protective layer may be bonded to the polarizing layer using an adhesive such as an adhesive, water glue, or ultraviolet (UV) curable adhesive, or a surface treatment such as a hard coat (HC) on the surface of the polarizer. The protective layer may be formed by applying

  The thickness of the polarizing layer is preferably 2 to 10 μm. When the thickness is less than 2 μm, the glass strength is insufficient, and when the thickness exceeds 10 μm, the meaning of thinning is reduced.

(Λ / 4 retardation layer)
The λ / 4 retardation layer refers to a film in which the in-plane retardation of the film is about ¼ with respect to a predetermined light wavelength (usually in the visible light region). The λ / 4 retardation layer is a broadband λ / 4 retardation film having a phase difference of approximately 1/4 of the wavelength in the visible light wavelength range in order to obtain almost perfect circularly polarized light in the visible light wavelength range. Preferably there is.

  The in-plane retardation Ro and the film thickness direction retardation Rt of the λ / 4 retardation layer of the present embodiment are expressed by the following equations, respectively. Note that the value of the phase difference can be calculated by measuring the birefringence at each wavelength in an environment of 23 ° C. and 55% RH using, for example, Axoscan manufactured by Axometrcs.

Ro = (nx−ny) × d
Rt = [(nx + ny) / 2−nz] × d
In the formula, nx, ny, and nz are refractive indexes at 550 nm measured in an environment of 23 ° C. and 55% RH, respectively, and nx is the maximum refractive index in the plane of the film (in the slow axis direction). Ny is the refractive index in the direction perpendicular to the slow axis in the film plane, nz is the refractive index in the thickness direction perpendicular to the film plane, and d is the film thickness (nm). ).

  The in-plane retardation Ro of the λ / 4 retardation layer may be 115 to 160 nm, preferably 120 to 160 nm, and more preferably 130 to 150 nm. When Ro exceeds the range of 115 to 160 nm, the phase difference at a wavelength of 550 nm does not become a quarter wavelength. When a long circular polarizing plate is produced using such a film and applied to, for example, an organic EL display In addition, the reflection of indoor lighting is intense, and there is a tendency that black color cannot be expressed in a bright place.

  The retardation Rt in the film thickness direction of the λ / 4 retardation layer is preferably in the range of 60 to 200 nm, more preferably in the range of 70 to 150 nm, and in the range of 70 to 100 nm. Is more preferable. When Rt exceeds the range of 60 to 200 nm, the hue when viewed obliquely on a large screen tends to deteriorate.

  The λ / 4 retardation layer is not particularly limited as long as it is an optically transparent resin. For example, acrylic resin, polycarbonate resin, cycloolefin resin, polyester resin, polylactic acid resin, polyvinyl alcohol type Resins, cellulose resins, and the like can be used.

  Among them, as the λ / 4 retardation layer, it is preferable to use a cellulose resin in consideration of heat resistance during the durability test.

In addition, the λ / 4 retardation layer has a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH measured in accordance with JIS Z 0208 in consideration of heat shock test resistance. And

(Resin layer)
From the viewpoint of improving the strength of the glass, it is preferable that a resin layer is formed on the side opposite to the λ / 4 retardation layer with respect to the thin film glass via an adhesive layer. The resin layer is not particularly limited as long as it is an optically transparent resin. For example, acrylic resin, polycarbonate resin, cycloolefin resin, polyester resin, polylactic acid resin, polyvinyl alcohol resin, and cellulose resin. Resin (cellulose derivative) etc. can be used.

  Among them, it is preferable to use a cellulose-based resin as the resin layer in consideration of heat resistance when forming the color filter.

  The resin layer preferably has a small in-plane direction retardation (retardation) Ro and a thickness direction retardation (retardation) Rt, more preferably, Ro is in the range of 0 to 5 nm, and Rt is −10. It is in the range of -10 nm.

The above Ro and Rt can also be obtained by the following method.
1) The obtained resin layer is conditioned at 23 ° C. and 55% RH. The average refractive index of the resin layer after humidity adjustment is measured with an Abbe refractometer.
2) Ro is measured with KOBRA 21ADH (manufactured by Oji Scientific Instruments) when light having a measurement wavelength of 590 nm is incident on the resin layer after humidity adjustment from the normal direction of the resin layer.
3) Retardation value R (θ) when light having a measurement wavelength of 590 nm is incident from the angle θ (incident angle (θ)) with respect to the normal direction of the resin layer by KOBRA 21ADH (manufactured by Oji Scientific Instruments). ). θ can be preferably 30 ° to 50 °.
4) nx, ny, and nz are calculated by KOBRA 21ADH (manufactured by Oji Scientific Instruments) from the measured Ro and R (θ) and the above-described average refractive index and film thickness, and the measurement wavelength is 590 nm. Rt at is calculated. The retardation can be measured after tempering for about 12 hours, for example, at 23 ° C. and 55% RH.

  The resin layer prepared in advance in the form of a film may be adhered to the glass via the adhesive layer, or the adhesive layer is formed on the glass, and the resin layer is directly applied or cast. May be formed.

In addition, in consideration of heat shock test resistance, the resin layer has a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH measured in accordance with JIS Z 0208.

  The resin layer preferably has a thickness of 5 μm or more from the viewpoint of reinforcing the thin film glass.

<Cellulosic resin (cellulose derivative)>
Examples of the cellulose resin (cellulose derivative) used in the present embodiment include cellulose ethers such as methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, cyanoethyl cellulose, triacetyl cellulose (TAC), diacetyl cellulose (DAC), and cellulose acetate. Examples include cellulose esters such as propionate (CAP), cellulose acetate butyrate (CAB), cellulose acetate phthalate, cellulose acetate trimellitate, and cellulose nitrate, with cellulose esters being preferred. Alternatively, aromatic carboxylic acid esters described in paragraph numbers [0010] to [0027] of JP-A No. 2002-179701 are used, and in particular, celluloses of paragraph numbers [0028] to [0036] of JP-A No. 2002-17979. Acylate is preferably used.

  Although there is no limitation in particular as a cellulose of the raw material of a cellulose resin, Cotton linter, a wood pulp, kenaf etc. can be mentioned. Moreover, although the cellulose resin obtained from these can be used individually or in mixture of arbitrary ratios, it is preferable to use 50 mass% or more of cotton linters.

  When the molecular weight of the cellulose ester is large, the elastic modulus is increased. However, when the molecular weight is excessively increased, the viscosity of the cellulose ester solution becomes too high, so that productivity is lowered. The molecular weight of the cellulose ester is preferably 70000-200000 in terms of number average molecular weight, more preferably 100000-200000. The cellulose ester used in the present embodiment preferably has a weight average molecular weight of Mw, a number average molecular weight of Mn, and a Mw / Mn ratio of 1.4 to 3.0, more preferably 1.4 to 2. 3.

  Since the average molecular weight and molecular weight distribution of cellulose ester can be measured using high performance liquid chromatography, the number average molecular weight (Mn) and the weight average molecular weight (Mw) are calculated using this, and the ratio is calculated. be able to. Measurement conditions are as follows.

Solvent: Methylene chloride Column: Shodex K806, K805, K803G (Used by connecting three Showa Denko Co., Ltd.)
Column temperature: 25 ° C
Sample concentration: 0.1% by mass
Detector: RI Model 504 (manufactured by GL Sciences)
Pump: L6000 (manufactured by Hitachi, Ltd.)
Flow rate: 1.0ml / min
Calibration curve: Standard polystyrene STK standard polystyrene (manufactured by Tosoh Corporation) Mw = 1,000,000-500 calibration curves with 13 samples were used. The 13 samples are preferably used at approximately equal intervals.

  The total acyl group substitution degree of the cellulose ester is preferably 1.0 to 2.9, more preferably 1.5 to 2.9. The total acyl group substitution degree can be measured according to ASTM-D817-96.

<Additive>
The resin film used for the λ / 4 retardation layer and the resin layer of the present embodiment includes a plasticizer that imparts processability, flexibility, and moisture resistance to the film, an ultraviolet absorber that imparts an ultraviolet absorption function, and slipperiness to the film. Fine particles (matting agent) for imparting odor, an antioxidant for preventing deterioration of the film, a retardation adjusting agent for adjusting the retardation of the film, and the like may be contained.

《Plasticizer》
There is no particular limitation on the plasticizer used, but it has a functional group capable of interacting with the adhesive layer so as not to cause haze or bleed out or volatilization from the film. preferable.

  Examples of such functional groups include hydroxyl groups, ether groups, carbonyl groups, ester groups, carboxylic acid residues, amino groups, imino groups, amide groups, imide groups, cyano groups, nitro groups, sulfonyl groups, sulfonic acid residues, Examples thereof include a phosphonyl group and a phosphonic acid residue, and a carbonyl group, an ester group and a phosphonyl group are preferred.

  Examples of such plasticizers include phosphate ester plasticizers, phthalate ester plasticizers, trimellitic acid ester plasticizers, pyromellitic acid plasticizers, polyhydric alcohol ester plasticizers, glycolate plasticizers. Agents, citrate plasticizers, fatty acid ester plasticizers, carboxylic acid ester plasticizers, polyester plasticizers, and the like can be preferably used. Particularly preferred are non-phosphate ester plasticizers such as polyhydric alcohol ester plasticizers, glycolate plasticizers, and polycarboxylic acid ester plasticizers.

  The polyhydric alcohol ester is composed of an ester of a dihydric or higher aliphatic polyhydric alcohol and a monocarboxylic acid, and preferably has an aromatic ring or a cycloalkyl ring in the molecule.

<Ultraviolet absorber>
The resin film used for the λ / 4 retardation layer and the resin layer of the present embodiment preferably contains an ultraviolet absorber from the viewpoint of preventing deterioration of the liquid crystal. A layer having an ultraviolet absorbing function may be formed on the resin film.

  As the ultraviolet absorber having an ultraviolet absorbing function, those having an excellent ability to absorb ultraviolet rays having a wavelength of 370 nm or less and little absorption of visible light having a wavelength of 400 nm or more are preferably used. Specific examples of preferably used ultraviolet absorbers include triazine compounds, oxybenzophenone compounds, benzotriazole compounds, salicylic acid ester compounds, benzophenone compounds, cyanoacrylate compounds, nickel complex compounds, and the like. However, it is not limited to these. Moreover, the polymeric ultraviolet absorber described in JP-A-6-148430 is also preferably used.

《Matting agent》
Fine particles such as a matting agent can be added to the resin film used for the λ / 4 retardation layer and the resin layer of this embodiment in order to impart slipperiness. Examples of the fine particles include fine particles of an inorganic compound or fine particles of an organic compound.

  Examples of the inorganic compound include fine particles such as silicon dioxide, titanium dioxide, aluminum oxide, zirconium oxide, and tin oxide. In this, it is preferable that it is a compound containing a silicon atom, and especially a silicon dioxide fine particle is preferable. Examples of the silicon dioxide fine particles include AEROSIL 200, 200V, 300, R972, R972V, R974, R202, R812, R805, OX50, and TT600 manufactured by Aerosil Co., Ltd.

  Examples of the organic compound include acrylic resin, silicone resin, fluorine compound resin, and urethane resin.

"Antioxidant"
Antioxidants are also referred to as deterioration inhibitors. When the liquid crystal display device is placed in a high humidity and high temperature state, the optical film may be deteriorated. Antioxidants have the role of delaying or preventing the optical film from being decomposed by, for example, the residual solvent amount of halogen in the optical film or phosphoric acid of the phosphoric acid plasticizer, so it is contained in the optical film. It is preferable to do so.

  As such an antioxidant, a hindered phenol compound is preferably used, and in particular, 2,6-di-t-butyl-p-cresol, pentaerythrityl-tetrakis [3- (3,5-di- -T-butyl-4-hydroxyphenyl) propionate] and triethylene glycol-bis [3- (3-t-butyl-5-methyl-4-hydroxyphenyl) propionate] are preferred. Further, for example, hydrazine-based metal deactivators such as N, N′-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionyl] hydrazine and tris (2,4-di- A phosphorus processing stabilizer such as t-butylphenyl) phosphite may be used in combination.

(Adhesive layer)
As the adhesive layer, a cocondensate of an inorganic reactive metal compound and an organic hydroxyl group-containing polymer compound is used. In the adhesive layer, by containing a metallic hydroxyl group that can be covalently bonded to the thin film glass, a λ / 4 retardation layer, and an organic hydroxyl group-containing polymer compound that is highly compatible and compatible with the organic component in the resin layer. The thin film glass and the λ / 4 retardation layer, and the thin film glass and the resin layer can be bonded. For the condensation reaction, a generally known method can be used. Hydrolysis condensation by addition of a catalyst or dehydration condensation by heating may be used.

<Hydrolysis catalyst>
The reactive polycondensable reactive metal compound that is an inorganic compound can use an acid such as hydrochloric acid, acetic acid, or citric acid as a hydrolysis catalyst, but a solid catalyst is preferably used. Further, water and another catalyst as required may be added to cause hydrolysis to accelerate the condensation reaction. The hydrolysis may be complete hydrolysis in which all hydrolyzable groups are hydrolyzed, but is particularly preferably partial hydrolysis in which only a part is hydrolyzed.

  The water added for the hydrolysis is preferably used in the range of 0.5 to 10 mol per 1 mol of the reactive metal compound and hydrolyzed with the solid catalyst. If the amount of water used for the hydrolysis is small, the hydrolysis of the alkoxy group becomes insufficient, resulting in a problem that only a few hydroxyl groups are generated. Preferably, the amount of water used is 0.5-4 moles per mole of reactive metal compound.

It is also preferable to use ion exchange water as water. Ion-exchanged water is preferable for hydrolyzing the reactive metal compound, and ion-exchanged water having an electric conductivity of 10 ¹⁰ MΩ or more is preferably used. If the electrical conductivity is lower than this, the ions contained in the ion exchange resin and the hydrolyzed water will undergo ion exchange, the pH of the hydrolyzed water will fluctuate greatly, and the hydrolyzed polycondensate generated will be present with great stability. This is not preferable. The electric conductivity of ion exchange water is more preferably 10 ¹² MΩ or more, and further preferably 10 ¹⁵ MΩ or more.

  In addition, when water is added to a hydrophobic hydrolytic polycondensable reactive metal compound, methanol, ethanol, acetonitrile, etc. are used so that the hydrolytic polycondensable reactive metal compound and water can be easily mixed. It is preferable that a hydrophilic organic solvent is also added. In addition, when a hydroxyl group-containing polymer compound (for example, a cellulose derivative) and a reactive metal compound capable of hydrolysis polycondensation are mixed, a good solvent for the cellulose derivative is preferably added so that the cellulose derivative does not precipitate. . In addition, a good solvent means the organic solvent which has favorable solubility with respect to a cellulose derivative.

  The solid catalyst as the hydrolysis catalyst is not particularly limited, and those listed below can be used.

(1) Cation exchange resin:
Amberlite 15, Amberlite 200C, Amberlist 15 (above, manufactured by Rohm and Haas); Dowex MWC-1-H, Dowex 88, Dowex HCR-W2 (above, Dow Chemical Co.); Levacit SPC-108, Levacit SPC-118 (above, Bayer); Diaion RCP-150H (Mitsubishi Kasei); Sumikaion KC-470, Duolite C26-C, Duolite C-433, Duolite-464 (The above, manufactured by Sumitomo Chemical Co., Ltd.); Nafion-H (manufactured by DuPont) and the like.

(2) Anion exchange resin:
Amberlite IRA-400, Amberlite IRA-45 (above, manufactured by Rohm and Haas) and the like.

(3) Inorganic solid in which a group containing a protonic acid group is bonded to the surface:
Such as _{Zr (O 3 PCH 2 CH 2} SO 3 H) 2, Th (O 3 PCH 2 CH 2 COOH) 2.

(4) Polyorganosiloxane containing protonic acid groups:
Polyorganosiloxane having a sulfonic acid group.

(5) Heteropoly acid:
Cobalt tungstic acid, phosphomolybdic acid, etc.

(6) Isopolyacid:
Niobic acid, tantalum acid, molybdic acid, etc.

(7) Unitary metal oxide:
Alumina, chromia, zirconia, CaO, MgO, etc.

(8) Composite metal oxide:
Silica-alumina, silica-magnesia, silica-zirconia, zeolites and the like.

(9) Clay mineral:
Acid clay, activated clay, montmorillonite, kaolinite, etc.

(10) Metal sulfate:
LiSO ₄ , MgSO _{4 and the} like.

(11) Metal phosphate:
Zirconia phosphate, lanthanum phosphate, etc.

(12) Metal nitrate:
Such as _{LiNO 3, Mn (NO 3)} 2.

(13) Inorganic solid in which a group containing an amino group is bonded to the surface:
Solids obtained by reacting aminopropyltriethoxysilane on silica gel.

(14) Polyorganosiloxane containing amino groups:
Amino-modified silicone resin.

Among these, in the present embodiment, a cation exchange resin is particularly preferable. As a kind of cation exchange resin, first, a suspension polymer of polystyrene or divinylbenzene as a skeleton is preferable. The types of ion exchange resins are classified into a gel type and a macroporous type. However, the gel type resin does not have pores, and it is difficult for a substance involved in the reaction to enter the inside of the resin, so that the active sites are not effectively used. The macroporous resin has large pores, and a substance involved in the reaction can easily reach the active site, and the active site is effectively used. For this reason, it is preferable that the cation exchange resin used in this embodiment is a macroporous material whose pore volume is 0.1 ml / g or more as measured by a mercury injection method. The acidic group attached to the resin is a sulfone group, an acryl group, or the like, preferably an H ⁺ type, and more preferably a sulfone group. Examples of ion exchange resins that satisfy these requirements include Amberlyst 15 (manufactured by Rohm and Hers), Diaion PK-208H, PK-216H, PK-228H (manufactured by Mitsubishi Kasei), Burolite CT-175, CT -171, CT-169 (manufactured by Burolite) and the like. Among these, Burolite CT-175 (manufactured by Burolite) is particularly preferable.

  In this embodiment, after the addition of the ion exchange resin, stirring is performed to hydrolyze the reactive metal compound to obtain a hydrolyzate or a condensate thereof. In this case, the stirring time (reaction time) ) Is preferably 3 minutes or more, particularly preferably 5 minutes or more. Moreover, it is preferable that reaction temperature shall be 0 degreeC or more. However, if the reaction time is too long, the molecular weight of the condensate becomes so large that haze may be increased. The same applies to the case where the reaction temperature is high, and the reaction temperature is preferably 0 to 50 ° C.

  Although there is no restriction | limiting in particular as a particle size of the cation exchange resin used by this embodiment, The range whose average particle diameter is 10-2000 micrometers is preferable. When the average particle size is less than 10 μm, filterability and liquid breakage may be deteriorated during resin separation after treatment. When the average particle size exceeds 2000 μm, the surface area per mass decreases, and the hydrolysis efficiency There is a problem that is low. Although it is preferable that the particle diameters are uniform, a chipped or cracked particle may be partially mixed.

  The ion exchange capacity of the ion exchange resin is preferably 0.1 milliequivalent / ml or more. If it is less than 0.1 milliequivalent / ml, the hydrolysis efficiency is lowered and productivity may be lowered.

  In this embodiment, the addition amount of the ion exchange resin as a solid catalyst is preferably 0.00001 to 30% by mass, more preferably 0.001 based on the reactive metal compound capable of hydrolysis polycondensation. ˜20 mass%. If the amount of the ion exchange resin is too large, the condensation proceeds preferentially, and the molecular weight of the condensate becomes too large. Moreover, when there is too little quantity of an ion exchange resin, sufficient activity required for a hydrolysis cannot be obtained, and a hydrolyzate or its condensate cannot fully be obtained.

  In the hydrolysis method using the solid catalyst in the present embodiment, water and alcohol are mixed in advance, a reactive metal compound is added and mixed therein, and then the solid catalyst is added and stirred to proceed the hydrolysis. It is preferable. In addition, it is also preferable that water and alcohol are mixed in advance and the solid catalyst is added thereto, and then the reactive metal compound is further added with stirring to proceed the hydrolysis.

<Reactive metal compound>
In the present embodiment, the term “metal” refers to “Chemistry of Periodic Table” by Iwanami Shoten, Kazuo Saito, p. 71. A metal according to 71, that is, a metal containing a semimetallic atom.

  Examples of the reactive metal compound capable of hydrolysis polycondensation used in this embodiment include metal alkoxide, metal diketonate, metal alkyl acetoacetate, metal isocyanate, and reactive metal halide. Preferably, the metal species is an alkoxide of Si, Ti, Zr or Al, and particularly preferably an alkoxide of Si.

  Such a reactive polycondensable reactive metal compound has M as the central metal, q as the number of atoms, A as the non-hydrolyzed substituent, p as the number of substituents, B as the hydrolyzable substituent, When r is the number of substituents, the reaction is ideally completed as shown in the following formula (1), and a metal oxide is obtained.

Equation _{(1) A p M q B} r → A p M q O r / 2

The hydrolyzable polycondensable reactive metal compound, in A _p M _q B _r shown in equation (1), such that p = 0, all being substituted with hydrolyzable substituents However, from the viewpoint of reducing the moisture permeability of the base film, a compound substituted with one, two, or three per atom of the metal by a non-hydrolyzed substituent may be included. . The amount of the metal compound having a substituent that is not hydrolyzed is preferably 50 mol% or less of the metal compound to be added. Moreover, you may use together 2 or more types of different types of metal alkoxide in the range of the said addition amount.

  As such a non-hydrolyzed substituent, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group is preferable. As the substituent of the alkyl group or aryl group, an alkyl group (for example, methyl group, ethyl group) Group), cycloalkyl group (eg cyclopentyl group, cyclohexyl group etc.), aralkyl group (eg benzyl group, 2-phenethyl group etc.), aryl group (eg phenyl group, naphthyl group etc.), heterocyclic group (eg furan, Thiophene, pyridine etc.), alkoxy group (eg methoxy group, ethoxy group etc.), aryloxy group (eg phenoxy group etc.), acyl group, halogen atom, cyano group, amino group, alkylthio group, glycidyl group, vinyl group, fluorine Examples thereof include an atom-containing alkyl group and a fluorine atom-containing aryl group.

  Examples of the reactive metal compound capable of polycondensation used in this embodiment include silicon compounds such as tetramethoxysilane, tetraethoxysilane, tetraisopropoxysilane, tetra-n-butoxysilane, and tetra-t-butoxysilane. , Tetrakis (methoxyethoxy) silane, tetrakis (methoxypropoxy) silane, tetrachlorosilane, tetraisocyanatosilane and the like.

  Examples of silicon compounds having substituent groups that are not hydrolyzed include dimethyldimethoxysilane, dimethyldiethoxysilane, dimethyldiisopropoxysilane, dimethyldibutoxysilane, diethyldimethoxysilane, diethyldiethoxysilane, diethyldiisopropoxysilane, and diethyldiisosilane. Butoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, diphenyldiisopropoxysilane, diphenyldibutoxysilane, 3-glycidoxypropylmethyldimethoxysilane, dichlorodimethylsilane, dichlorodiethylsilane, methyltrimethoxysilane, methyltriethoxysilane , Methyltriisopropoxysilane, methyltributoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, ethyltriiso Lopoxysilane, ethyltributoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltriisopropoxysilane, phenyltributoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltriisopropoxysilane, vinyltributoxysilane, 3 -Glycidoxypropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-chloropropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, (3 -Acryloxypropyl) trimethoxysilane, acetoxytriethoxysilane, (heptadecafluoro-1,1,2,2-tetrahydrodecyl) trimethoxysilane, (3,3,3 (Trifluoropropyl) trimethoxysilane, methyltrichlorosilane, ethyltrichlorosilane, phenyltrichlorosilane, (3,3,3-trifluoropropyl) triethoxysilane, pentafluorophenylpropyltrimethoxysilane, (heptadecafluoro-1,1 , 2,2-Tetrahydrodecyl) triethoxysilane, (3,3,3-trifluoropropyl) trichlorosilane, pentafluorophenylpropyltrichlorosilane, (heptadecafluoro-1,1,2,2-tetrahydrodecyl) trichlorosilane Methyl triisocyanate silane, phenyl triisocyanate silane, vinyl triisocyanate silane, and the like. In addition, quantified silicon compounds such as silicate 40, silicate 45, silicate 48, and M silicate 51 manufactured by Tama Chemical, which are partially condensed with these compounds, may be used.

  In addition, as titanium compounds, titanium methoxide, titanium ethoxide, titanium isopropoxide, titanium-n-butoxide, tetrachlorotitanium, titanium diisopropoxide (bis-2,4-pentanedionate), titanium diiso Propoxide (bis-2,4-ethylacetoacetate), titanium di-n-butoxide (bis-2,4-pentanedionate), titanium acetylacetonate, titanium lactate, titanium triethanolamate, butyl titanate dimer, etc. Can be mentioned.

  Further, as the zirconium compound, zirconium-n-propoxide, zirconium-n-butoxide, zirconium tri-n-butoxide acetylacetonate, zirconium di-n-butoxide bisacetylacetonate, zirconium acetylacetonate, zirconium acetate, etc. Is mentioned.

  Examples of the aluminum compound include aluminum ethoxide, aluminum isopropoxide, aluminum n-butoxide, aluminum s-butoxide, aluminum di-s-butoxide ethylacetylacetonate, aluminum tert-butoxide, almatrane, aluminum phenoxide. , Aluminum acetylacetonate, aluminum ethylacetylacetonate and the like.

  Examples of the compound composed of other metals include barium isopropoxide, calcium ethoxide, copper ethoxide, magnesium ethoxide, manganese methoxide, strontium isopropoxide, tin ethoxide, zinc methoxyethoxide, trimethoxyborane, Triethoxyborane, antimony ethoxide, arsenic triethoxide, bismuth t-pentoxide, chromium isopropoxide, erbium methoxyethoxide, gallium ethoxide, indium methoxyethoxide, iron ethoxide, lanthanum isopropoxide, neodymium methoxyethoxide, praseodymium methoxy Ethoxide, samarium isopropoxide, vanadium triisobutoxide oxide, yttrium isopropoxide, tetramethoxygermane, tetra Toxigermane, tetraisopropoxygermane, tetra-n-butoxygermane, cerium-t-butoxide, hafnium ethoxide, hafnium-n-butoxide, tellurium ethoxide, molybdenum ethoxide, niobium ethoxide, niobium-n-butoxide, tantalum Examples thereof include methoxide, tantalum ethoxide, tantalum-n-butoxide, tungsten (V) ethoxide, tungsten (VI) ethoxide, tungsten (VI) phenoxide, and the like.

  The reactive metal compound capable of polycondensation used in this embodiment may be a compound called double metal alkoxide having two metal atoms in the molecular species. Examples of such double metal alkoxides include aluminum copper alkoxide, aluminum titanium alkoxide, aluminum yttrium alkoxide, aluminum zirconium alkoxide, barium titanium alkoxide, barium yttrium alkoxide, barium zirconium alkoxide, indium tin alkoxide, lithium nickel alkoxide manufactured by Gerest Co., Ltd. Lithium niobium alkoxide, lithium tantalum alkoxide, magnesium aluminum alkoxide, magnesium titanium alkoxide, magnesium zirconium alkoxide, strontium titanium alkoxide, strontium zirconium alkoxide, etc., but at least silicon, aluminum, titanium, zirconium Preferably one that contains any metal.

<Hydroxyl-containing polymer compound>
The hydroxyl group-containing polymer compound only needs to contain a hydroxyl group in the molecule, and examples thereof include synthetic polymers such as polyvinyl alcohol, polysaccharides such as starch, cellulose, carboxymethyl cellulose, sodium alginate, and derivatives thereof. It is done. These hydroxyl group-containing polymer compounds can be used singly or in appropriate combination of two or more.

  Synthetic polymers include, for example, vinyl-based, polystyrene-based, polyacrylic-based, polyurethane-based, alkyd-based, melamine-based, urea-based, phenol-based, polyester-based, polyglycerol-based polymer compounds having a hydroxyl group, and multi-branched shapes. A high molecular compound having a hydroxyl group having can be used. Further, the polymer having a hydroxyl group may be a polymer into which a monomer having a hydroxyl group is introduced. In this case, the amount of hydroxyl groups and the introduction position of the polymer can be adjusted.

  Examples of the monomer having a hydroxyl group include styrenes having a hydroxyl group such as 3-vinylphenol, hydroxymethylstyrene, 4-vinylbenzyl-4-hydroxybutyl ether, 4- (hydroxymethylsilylphenyl) styrene, and hydroxyethyl methacrylate. An acrylic resin having a hydroxyl group such as acrylamide, an acrylamide resin having a hydroxyl group such as N- (4- (4-hydroxyphenylsulfonyl) phenoxycarbonyl) methacrylamide, and the like can be used, and a vinyl monomer is preferable. Two or more kinds of these monomers having a hydroxyl group may be mixed and used.

  Polysaccharides include starch, hydroxymethyl starch, hydroxyethyl starch, hydroxypropyl starch, glycogen, inulin, lichenin, cellulose, hemicellulose, amylopectin, heparin, heparitin sulfate, chondroitin sulfate, hyaluronic acid, keratosulfate, chitin, chitosan, agar , Carrageenan, alginic acid, fur celerane, locust bean gum, galactomannan, guar gum, syrup gum, tamarind gum, gum arabic, tragacanth gum, caraya gum, pectin, arabinogalactan, xanthan gum, gellan gum, pullulan, dextran, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxy Propylmethylcellulose, carboxymethylcellulose, methylcellulose Scan, ethylcellulose, and the like of these cationic products can be mentioned.

  As the hydroxyl group-containing polymer compound used in the present embodiment, cellulose derivatives are preferably used. Among them, diacetyl cellulose (DAC), cellulose acetate propionate (CAP), cellulose acetate butyrate (CAB), cellulose acetate phthalate, cellulose Cellulose esters such as acetate trimellitate and cellulose nitrate are preferred. More preferably, the acyl group substitution degree is 0.5 to 2.9, and more preferably, the acyl group substitution degree is 1.0 to 2.6.

〔Example〕
Hereinafter, specific examples of the present invention will be described as examples. For comparison with the present invention, comparative examples will also be described. The present invention is not limited to the following examples. In the following description, “parts” or “%” indicates “parts by mass” or “mass%” unless otherwise specified.

<Film A>
As film A constituting the first or second resin layer, KC2UA, which is a cellulose ester film manufactured by Konica Minolta Advanced Layer Co., Ltd., was prepared.

<Manufacture of film B>
<Silicon dioxide dispersion diluent>
Aerosil R812 (manufactured by Nippon Aerosil Co., Ltd.) 10 parts by mass Ethanol 90 parts by mass The above was stirred and mixed with a dissolver for 30 minutes, and then dispersed with Manton Gorin to obtain a silicon dioxide dispersion. 88 parts by mass of methylene chloride was added to this silicon dioxide dispersion with stirring, and the mixture was stirred and mixed with a dissolver for 30 minutes. Subsequently, a fine particle dispersion dilution filter (Advantech Toyo Co., Ltd .: Polypropylene Wind Cartridge Filter TCW-PPS- 1N) to prepare a silicon dioxide dispersion dilution.

<Preparation of dope solution>
TAC: Triacetyl cellulose (acetyl group substitution degree 2.89, Mw = 19000, Ca content 25 ppm) 100 parts by mass Tinuvin 928 (manufactured by BASF Japan Ltd.) 2.5 parts by mass Polycondensed ester compound P2 7.0 parts by mass Part Polycondensed ester compound P5 1.6 parts by mass Methylene chloride 540 parts by mass Ethanol 35 parts by mass The above was put into a sealed container, completely dissolved while heating and stirring, and filtered. To this, 4 parts by mass of a silicon dioxide dispersion diluted solution was added with stirring, and the mixture was further stirred for 30 minutes to prepare a dope solution.

<Synthesis of Polycondensed Ester Compound P2>
Said polycondensation ester compound P2 was synthesize | combined as follows. 251 g of 1,2-propylene glycol, 244 g of phthalic anhydride, 103 g of adipic acid, 610 g of benzoic acid, 0.191 g of tetraisopropyl titanate as an esterification catalyst, 2 L four-neck equipped with thermometer, stirrer, and slow cooling tube The flask was charged and gradually heated with stirring until it reached 230 ° C. in a nitrogen stream. Then, a dehydration condensation reaction was carried out while observing the degree of polymerization. After completion of the reaction, unreacted 1,2-propylene glycol was distilled off under reduced pressure at 200 ° C. to obtain a polycondensed ester compound P2. The acid value was 0.10 and the number average molecular weight was 450.

<Synthesis of polycondensed ester compound P5>
Said polycondensation ester compound P5 was synthesize | combined as follows. 251 g of 1,2-propylene glycol, 354 g of terephthalic acid, 680 g of p-troyl acid and 0.191 g of tetraisopropyl titanate as an esterification catalyst are charged into a 2 L four-necked flask equipped with a thermometer, a stirrer and a slow cooling tube. The temperature was gradually raised with stirring until it reached 230 ° C. in a nitrogen stream. Then, a dehydration condensation reaction was carried out while observing the degree of polymerization. After completion of the reaction, unreacted 1,2-propylene glycol was distilled off under reduced pressure at 200 ° C. to obtain a polycondensed ester compound P5. The acid value was 0.30 and the number average molecular weight was 400.

<Film formation / stretching / drying>
Next, using the belt casting apparatus, the above cellulose acylate dope solution was cast uniformly on a stainless steel belt support at a temperature of 35 ° C. and a width of 2 m. With the stainless steel belt support, the solvent was evaporated until the residual solvent amount reached 100% by mass, and it was peeled off from the stainless steel belt support. The peeled film web was conveyed while being dried at 50 ° C., slitted, and then stretched by a tenter in a TD direction (direction perpendicular to the film conveying direction) at a temperature of 160 ° C. and a stretching ratio of 26%. . At this time, the residual solvent amount when starting stretching with a tenter was 5.0%. Then, after drying for 15 minutes while transporting the inside of a drying apparatus at 120 ° C. with a number of rolls, slitting is performed, and both ends of the film are knurled with a width of 15 mm and a height of 5 μm. Obtained. The residual solvent amount of the film was less than 0.1%, the film thickness was 10 μm, the width was 2 m, and the winding length was 6000 m. The draw ratio in the MD direction (film transport direction) calculated from the rotational speed of the stainless steel belt support and the operating speed of the tenter was 1.05.

<Film C>
As a film C constituting the first or second resin layer, KC4UA which is a cellulose ester film manufactured by Konica Minolta Advanced Layer Co., Ltd. was prepared.

<Manufacture of film D>
<Preparation of dope solution>
Delpet 80N (MMA and MA (methyl acrylate) copolymer acrylic resin, manufactured by Asahi Kasei Chemicals, Mw = 100000) 100 parts by weight Methylene chloride 300 parts by weight Ethanol 40 parts by weight Charged into a sealed main melting kettle The solution was dissolved while stirring to prepare a dope solution.

<Film formation / stretching / drying>
The dope solution was uniformly cast on a stainless belt support at a temperature of 22 ° C. and a width of 2 m using a belt casting apparatus. With the stainless steel belt support, the solvent was evaporated until the residual solvent amount reached 100%, and peeling was performed from the stainless steel belt support with a peeling tension of 162 N / m. The peeled acrylic resin web was evaporated at 35 ° C., slit to 1.6 m width, and then dried at a drying temperature of 135 ° C. while stretching 1.3 times in the TD direction with a tenter. At this time, the residual solvent amount when starting stretching with a tenter was 10%. After stretching with a tenter, relaxation was performed at 130 ° C. for 5 minutes, and then drying was completed while transporting a drying zone at 120 ° C. and 130 ° C. with many rolls, slitting to a width of 1.5 m, and a width of 10 mm at both ends of the film. A knurling process having a height of 5 μm was applied, and the film was wound on a core having an inner diameter of 6 inches with an initial tension of 220 N / m and a final tension of 110 N / m. The draw ratio in the MD direction calculated from the rotational speed of the stainless steel belt support and the operating speed of the tenter was 1.1 times. The film thickness was 20 μm and the number of turns was 4000 m.

<Film E>
As a film E constituting the first or second resin layer, KC4DR which is a cellulose ester film manufactured by Konica Minolta Advanced Layer Co., Ltd. was prepared.

<Manufacture of film F>
<Fine particle dispersion>
Fine particles (Aerosil R812 manufactured by Nippon Aerosil Co., Ltd.) 11 parts by weight Ethanol 89 parts by weight The above was stirred and mixed with a dissolver for 50 minutes, and then dispersed with Manton Gorin to obtain a fine particle dispersion.

<Fine particle additive solution>
The fine particle dispersion was slowly added to the dissolution tank containing methylene chloride with sufficient stirring. Further, the particles were dispersed by an attritor so that the secondary particles had a predetermined particle size. This was filtered through Finemet NF manufactured by Nippon Seisen Co., Ltd. to prepare a fine particle additive solution.
99 parts by mass of methylene chloride 5 parts by mass of fine particle dispersion

<Preparation of dope solution>
Methylene chloride 340 parts by mass Ethanol 64 parts by mass Cellulose ester (acetyl group substitution degree 2.45, Mn = 60000)
100 parts by mass Sugar ester compound M 12 parts by mass Particulate additive solution 1 part by mass The above was put into a sealed main dissolution vessel and dissolved with stirring to prepare a dope solution.

<Synthesis of sugar ester compound M>
The sugar ester compound M was synthesized as follows. Four-headed Kolben equipped with a stirrer, a reflux condenser, a thermometer, and a nitrogen gas inlet tube were charged with 34.2 g (0.1 mol) of sucrose, 135.6 g (0.6 mol) of benzoic anhydride, 284. 8 g (3.6 mol) was charged, the temperature was raised while bubbling nitrogen gas through a nitrogen gas introduction tube with stirring, and an esterification reaction was carried out at 70 ° C. for 5 hours.

Next, the inside of the Kolben was depressurized to 4 × 10 ² Pa or less, and after excess pyridine was distilled off at 60 ° C., the inside of the Kolben was depressurized to 1.3 × 10 Pa or less and the temperature was raised to 120 ° C. Most of the acid and benzoic acid formed were distilled off. Then, 1 L of toluene and 300 g of a 0.5% by mass aqueous sodium carbonate solution were added, and the mixture was stirred at 50 ° C. for 30 minutes and then allowed to stand to separate a toluene layer. Finally, 100 g of water is added to the collected toluene layer, and after washing with water at room temperature for 30 minutes, the toluene layer is separated, and toluene is distilled off at 60 ° C. under reduced pressure (4 × 10 ² Pa or less). The sugar ester compound M which is a mixture of A-1, A-2, A-3, A-4, A-5, etc. was obtained.

  When the obtained mixture was analyzed by high performance liquid chromatography-mass spectrometry (HPLC-MS), A-1 was 1.2% by mass, A-2 was 13.2% by mass, and A-3 was 14.2% by mass. %, A-4 was 35.4% by mass, A-5 and the like were 40.0% by mass. The average degree of substitution was 5.2. Compounds A-1, A-2, A-3, A-4, A-5 and the like are represented by the following structural formulas.

<Film formation / stretching / drying>
Using a belt casting apparatus, the solvent was evaporated until the residual solvent amount in the cast (cast) film was 75% on a stainless belt support using a belt casting apparatus. Subsequently, it peeled from the stainless steel belt support body with peeling tension 130N / m. The peeled film was stretched 35% in the TD direction using a tenter while applying heat at 170 ° C. The residual solvent at the start of stretching was 15%. Next, drying was completed while conveying the drying zone with a large number of rolls. The drying temperature was 130 ° C. and the transport tension was 100 N / m. As described above, a film F having a dry film thickness of 38 μm was obtained.

<Evaluation of Films A to F>
The moisture permeability of the films A to F was measured from the change in mass of calcium chloride by the cup method under the conditions of 40 ° C. and 90% RH based on the JISZ0208 method. Table 1 shows the moisture permeability of the films A to F.

<Manufacture of adhesive A>
After mixing the materials in the following ratio and stirring at room temperature, the solid catalyst was separated by filtration to prepare an adhesive A containing a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound.
Acetone 100 parts by mass Tetraethoxysilane (TEOS) 10 parts by mass Amberlyst 15 (solid catalyst) 2 parts by mass Cellulose ester (DAC, acetyl group substitution degree 2.45) 10 parts by mass

<Manufacture of adhesive B>
After mixing the materials in the following ratio and stirring at room temperature, the solid catalyst was separated by filtration to prepare an adhesive B containing a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound.
Acetone 100 parts by weight Tetramethoxysilane (TMOS) 10 parts by weight Amberlyst 15 (solid catalyst) 2 parts by weight Cellulose ester (DAC, acetyl group substitution degree 2.45) 10 parts by weight

<Example 1>
A glass laminate of Example 1 was obtained by preparing a thin film glass having a thickness of 50 μm manufactured by Nippon Electric Glass Co., Ltd., and heat-bonding the film A with an adhesive A on one side.

<Example 2>
A glass laminate of Example 2 was obtained in the same manner as in Example 1 except that the adhesive B was used instead of the adhesive A.

<Example 3>
A glass laminate of Example 3 was obtained in the same manner as in Example 1 except that the film B was used instead of the film A.

<Example 4>
A glass laminate of Example 4 was obtained in the same manner as in Example 1 except that the film E was used instead of the film A.

<Example 5>
A glass laminate of Example 5 was obtained in the same manner as in Example 1 except that the film F was used instead of the film A.

<Example 6>
A glass laminate of Example 6 was obtained by preparing a thin film glass having a thickness of 50 μm manufactured by Nippon Electric Glass Co., Ltd. and heat-bonding film A with adhesive A on both sides thereof.

<Example 7>
A glass laminate of Example 7 was obtained in the same manner as Example 6 except that the film E was used instead of the single-sided film A.

<Example 8>
A glass laminate of Example 8 was obtained in the same manner as in Example 6 except that the film F was used instead of the single-sided film A.

<Comparative Example 1>
A glass laminate of Comparative Example 1 was obtained in the same manner as in Example 1 except that an acrylic pressure-sensitive adhesive (PSA) was used instead of the adhesive A.

<Comparative example 2>
A glass laminate of Comparative Example 2 was obtained in the same manner as in Example 1 except that the film C was used instead of the film A.

<Comparative Example 3>
A glass laminate of Comparative Example 3 was obtained in the same manner as in Example 1 except that the film D was used instead of the film A.

<Comparative Example 4>
A glass laminate of Comparative Example 4 was obtained in the same manner as in Example 6 except that the film C was used instead of the double-sided film A.

<Evaluation of Examples and Comparative Examples>
Table 2 shows the results of evaluating the resistance by heat shock tests for the glass laminates of Examples 1 to 8 and Comparative Examples 1 to 4.

  The method and evaluation criteria of the heat shock test are as follows. Each glass laminate was stored at -30 ° C for 30 minutes, and then stored at 95 ° C for 30 minutes in a thermal shock device TSE-11 manufactured by ESPEC Corporation, and this was treated as one cycle for a total of 500 cycles (500 hours). Went. And the state of the glass laminated body after a test was judged visually according to the following evaluation criteria.

(Evaluation criteria)
○: There is no floating or peeling in the glass laminate △: There is a slight float or peeling in the glass laminate, but there is no problem in actual use ×: There is a large peeling in the glass laminate, causing a problem in actual use

  From Table 2, in Comparative Example 1 in which the first adhesive that bonds the thin film glass and the first resin layer is an acrylic pressure-sensitive adhesive, a large peeling occurred in the glass laminate in the heat shock test. In Examples 1 and 2 containing TEOS (or TMOS) and DAC as raw materials for the first adhesive, the glass laminate did not float or peel off in the heat shock test. This is because the first adhesive contains a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound, thereby improving the adhesion between the thin film glass and the first resin layer. This is thought to be because the dimensional change of the first resin layer due to environmental fluctuations in the heat shock test is suppressed.

  Further, from Table 2, when the case where the resin layer is bonded to one side of the thin film glass is seen, in Comparative Example 2 using the film C as the first resin layer and Comparative Example 3 using the film D as the first resin layer, In spite of using the adhesive A, a large peeling occurred in the glass laminate in the heat shock test. On the other hand, in Example 1 using the film A for the first resin layer, Example 3 using the film B, Example 4 using the film E, and Example 5 using the film F, the adhesive is used. By using A, the glass laminate did not float or peel off in the heat shock test, or peeling that would cause a problem in actual use did not occur.

This is because the films C and D used in Comparative Examples 2 and 3 are low moisture-permeable films with a moisture permeability of less than 1000 g / m ² · 24 hr, so that when bonded with the adhesive A, alkoxy group hydrolysis or alkoxy Alcohol generated by the condensation reaction of the group and the hydroxyl group remains in the adhesive A, and in that state, the heat shock test is performed. As a result, a reverse reaction occurs due to the heated alcohol, the condensation is released, and the adhesive strength is reduced. It is considered that the glass and the first resin layer were peeled off.

On the other hand, since the films A, B, E, and F used in Examples ¹ and 3 to 5 are highly moisture permeable films having a moisture permeability of 1000 g / m ² · 24 hr or more, when pasted with the adhesive A It is considered that the alcohol generated in the test can be quickly released, the reverse reaction does not occur even in the heat shock test, and the adhesive force can be maintained after the heat shock test. In addition, it can be said that heat shock test tolerance is so high that moisture permeability is high.

  Further, from Table 2, when the case where the resin layers are bonded to both surfaces of the thin film glass is seen, in Comparative Example 4 in which the film C is used for the first and second resin layers, the adhesive A is used. In the heat shock test, large peeling occurred on the glass laminate. On the other hand, Example 6 using film A for the first resin layer and film A for the second resin layer, Example 7 using film E for the second resin layer, second resin In Example 8 using the film F as a layer, by using the adhesive A, the glass laminate did not float or peel off in the heat shock test, or peeling that caused a problem in actual use did not occur. This is a result according to the case where the resin layer is bonded to one side of the thin film glass, which is considered to be due to the same reason.

Therefore, as the first and second resin layers, a highly moisture permeable film having a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH measured in accordance with JIS Z 0208 is used. Therefore, it can be said that it has heat shock test resistance.

  As mentioned above, when the glass laminated body of Examples 1-8 is used for a display apparatus, it can be used for a long period of time without a problem, even if it is used for various uses and puts in various environments.

[Supplement]
In the present invention, the first and second resin layers are not particularly limited as long as the first and second resin layers can compensate for the flexibility and cracking property of the thin film glass and are optically transparent resins. Resins, cycloolefin resins, polyester resins, polylactic acid resins, polyvinyl alcohol resins, cellulose resins (cellulose derivatives), and the like can be used. And from a viewpoint of reinforcing thin film glass, it is desirable that the film thickness is 5 micrometers or more.

  Moreover, the extending | stretching direction of the film used in this invention may be any of an oblique direction, a vertical direction, or a horizontal direction.

  Further, it can be said that the organic EL display device and the liquid crystal display device described in the present embodiment may have the following configurations.

  The organic EL display device of this embodiment includes a polarizing plate that transmits linearly polarized light, and the above-described glass laminate and the polarizing plate may constitute a circularly polarizing plate.

  The liquid crystal display device of this embodiment includes a polarizing plate that transmits linearly polarized light, and the above-described glass laminate and the polarizing plate may constitute a circularly polarizing plate.

  In the organic EL display device or the liquid crystal display device, the polarizing plate may be bonded to the λ / 4 retardation layer of the glass laminate.

  The polarizing plate includes a polarizing layer that transmits linearly polarized light and a protective layer that protects one surface of the polarizing layer, and the polarizing layer may be bonded to the λ / 4 retardation layer.

  In the organic EL display device or the liquid crystal display device, the polarizing plate is configured such that a polarizing layer that transmits linearly polarized light is sandwiched between two protective layers from one side, and the other protective layer is a λ / 4 retardation layer. It may be pasted.

  The glass laminate of the present invention can be used for organic EL display devices and liquid crystal display devices.

DESCRIPTION OF SYMBOLS 1 Organic EL display device 2 Organic EL element 3 Glass laminated body 31 Thin film glass 32 Adhesive layer (1st adhesive agent)
33 λ / 4 retardation layer (first resin layer)
34 Adhesive layer (second adhesive)
35 Resin layer (second resin layer)
51 Liquid crystal display device 61 Substrate 62 Substrate 63 Liquid crystal layer

Claims (9)

The thin film glass and the first resin layer are bonded with the first adhesive,
The first adhesive includes a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound,
First resin layer, 40 ° C. which is measured in accordance with JIS Z 0208, the moisture permeability 90% RH is state, and are more 1000g ^/ m 2 · 24hr,
The glass laminate , wherein the hydroxyl group-containing polymer compound contained in the first adhesive contains a cellulose derivative .   The glass laminate according to claim 1, wherein the first resin layer contains a cellulose derivative. The glass laminate according to claim 1 or 2 , wherein the cellulose derivative contained in the first adhesive is a cellulose ester. The reactive metal compound contained in a 1st adhesive agent is a metal alkoxide, The glass laminated body in any one of Claims 1-3 characterized by the above-mentioned. The thin film glass and the first resin layer are bonded with the first adhesive,
The first adhesive includes a cocondensate of a reactive metal compound and a hydroxyl group-containing polymer compound,
The first resin layer has a moisture permeability of 1000 g / m ² · 24 hr or more at 40 ° C. and 90% RH measured in accordance with JIS Z 0208 ,
A second resin layer is bonded with a second adhesive on the side opposite to the side on which the first resin layer of the thin film glass is laminated,
The second adhesive is seen containing a co-condensation product of a reactive metal compound and a hydroxyl group-containing polymer compound,
Hydroxyl group-containing polymer compound contained in the second adhesive, wherein the to Ruga lath stack that contains a cellulose derivative. The glass laminate according to claim 5 , wherein the second resin layer contains a cellulose derivative. The glass laminate according to claim 5 or 6 , wherein the cellulose derivative contained in the second adhesive is a cellulose ester. The reactive metal compound contained in the second adhesive is a metal alkoxide, and the glass laminate according to any one of claims 5 to 7 . The glass laminate according to any one of claims 1 to 8 , wherein the thickness of the thin film glass is 5 to 100 µm.

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