JP5697900B2 - Heat ray shielding double-glazed glass - Google Patents

Description

  The present invention relates to a multilayer glass using a heat ray shielding glass having heat ray shielding properties or heat ray reflection properties.

  Conventionally, in order to reduce the air conditioning load of buildings such as office buildings and buses, passenger cars, trains, etc., railways, etc., these windows have a function of shielding near infrared rays (heat rays) in sunlight, There is a demand for a function of reflecting and insulating heat rays radiated from the room. As a glass that shields or reflects heat rays, a kneading type heat ray absorbing glass in which ions such as Fe, Cr, Ti, etc. are introduced into the glass itself to give heat ray absorption, or a heat ray reflecting glass in which a metal oxide film is deposited. A thin film of a transparent conductive film such as indium tin oxide (ITO) or tin oxide (ATO) is formed into a dry film, and a noble metal film / metal oxide film mainly composed of a metal oxide film / Ag film is laminated. A heat ray shielding glass (Patent Document 1) on which a heat ray shielding film (also referred to as Low-E film) is formed has been developed and put into practical use. Among these, the Low-E film has a function (heat insulation) that transmits near infrared rays of sunlight having a relatively short wavelength and does not escape by reflecting far infrared rays such as heating emitted from the room.

  Such heat ray-shielding glass (particularly, the one on which the Low-E film is formed) is arranged to be opposed to another glass plate with a predetermined interval (air layer) to form a multilayer glass. And what improved the heat insulation is also developed (patent document 2). Thereby, the energy consumption by air conditioning can be further reduced.

Further, as heat ray shielding glass having high heat ray shielding properties and realizing high visible light transmittance, fine particles of tungsten oxide and / or composite tungsten oxide (also referred to as (composite) tungsten oxide) and UV excitation coloring. The thing which formed the coating film containing an inhibitor on the glass substrate is developed (patent document 3).
Furthermore, the property of absorbing infrared rays is also known for conductive polymers, and is a transparent heat shield composed of a surface protective layer, a heat shield layer using a conductive polymer, a substrate, an ultraviolet absorbing layer, and an adhesive layer. A film has been developed (Patent Document 4).

JP 2001-226148 A JP 2007-70146 A JP 2007-269523 A JP 2005-288867 A

  However, since the Low-E film used for the heat ray shielding glass described in Patent Document 1 is formed by a vacuum film formation method such as a sputtering method, a large-sized device is required, and the manufacturing cost increases. In addition, the metal film is easily corroded, and there is a problem that appearance characteristics are deteriorated by long-term use. These also cause the same problem even when the multilayer glass described in Patent Document 2 is used.

  Moreover, although the heat ray shielding glass described in Patent Document 3 is excellent in the function of shielding the near-infrared ray of sunlight, it is satisfactory depending on the application because it has low heat insulation properties to reflect heat rays such as heating emitted from the room. Performance may not be obtained.

  On the other hand, the shielding film using the conductive polymer of Patent Document 4 cannot be said to have sufficient heat ray shielding properties. Further, according to the study by the present inventors, a heat ray shielding glass having a heat ray reflective layer made of a conductive polymer has high heat insulation properties depending on conditions, but durability in the presence of moisture (high humidity conditions) In the invention, it is also known as “water resistance”).

  Accordingly, an object of the present invention is to provide a heat ray shielding glass product that has excellent heat ray shielding properties, particularly heat insulation properties, can be produced at low cost, and has high durability in the presence of moisture (high humidity conditions). It is to provide.

The purpose is to provide a heat ray shielding glass having a glass plate and a heat ray reflective layer made of a conductive polymer provided on the surface of the glass plate and another glass plate, with the gap between the heat ray reflective layer and the heat ray reflective layer. most of which are arranged so as to face the glass plate, and the hollow layer is formed by the gap, and the surface resistance of the heat ray reflective layer is, 10000 ohms / □ Ri der less heat ray reflective layer of the heat ray shielding glass This is achieved by a heat-shielding double-glazed glass characterized in being located in the upper layer. The heat ray reflective layer made of a conductive polymer has high heat ray reflectivity (heat insulation), particularly if the surface resistance value is 10000Ω / □ or less, and the free electron density of the heat ray reflective layer becomes high, Sufficient heat insulation is obtained. In addition, since the conductive polymer is made of an organic polymer, it is possible to form a layer by a low-cost coating method or the like. Furthermore, by using the double-glazed glass as described above, the heat ray reflective layer made of a conductive polymer can be protected from moisture such as rainwater, condensation, moisture, etc., and is water resistant (in the presence of moisture (high humidity conditions) It is possible to obtain a heat ray-shielding glass product having a high durability in (below).

Preferred embodiments of the heat ray shielding multilayer glass of the present invention are as follows.
(1) The conductive polymer has the following formula (I):

(In the formula, R ¹ and R ² each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or R ¹ and R ² together may be optionally substituted carbon. An alkylene group having 1 to 4 atoms, and n represents an integer of 50 to 1000).

Since the above polythiophene derivative has high conductivity, it is suitable as a conductive polymer used for the heat ray reflective layer in the present invention.
(2) The heat ray reflective layer has a thickness of 10 to 3000 nm.
(3) The heat ray shielding glass is obtained by bonding a transparent plastic film having a heat ray reflective layer formed on a surface thereof and a glass plate via an adhesive layer.
Thereby, the impact resistance and penetration resistance of the heat ray shielding glass can be improved.
(4) The adhesive layer contains an ethylene-vinyl acetate copolymer (EVA).
EVA is highly transparent and excellent in weather resistance, and is therefore suitable as an adhesive used for the adhesive layer in the present invention.
(5) An ultraviolet absorbing layer is formed on the heat ray reflective layer on the side irradiated with sunlight. Thereby, deterioration due to ultraviolet rays of the conductive polymer can be further suppressed.
(6) The said hollow layer is formed when the said heat ray shielding glass and said another glass plate are arrange | positioned through a spacer. Furthermore, it is preferable to put a desiccant in the spacer.
(7) The hollow layer is one kind of layer selected from the group consisting of a dry air layer, an inert gas layer, and a reduced pressure layer. Thereby, the heat ray reflective layer made of a conductive polymer can be more sufficiently protected from moisture.

  According to the present invention, since the heat ray reflective layer of the heat ray shielding glass is formed of a conductive polymer and has a predetermined surface resistance value, it does not escape by reflecting heat rays such as heating radiated from the room. Has heat insulation. Further, since the conductive polymer is made of an organic polymer, a layer can be formed by a low-cost coating method or the like, and an inexpensive product can be obtained. Furthermore, since the heat ray shielding glass is a multi-layer glass arranged so that the heat ray reflective layer faces another glass plate, the heat ray reflective layer made of a conductive polymer can be protected from moisture such as rain water and moisture. And heat-shielding glass products with high water resistance.

It is a schematic sectional drawing which shows a typical example of the heat ray shielding multilayer glass of this invention.

  Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. FIG. 1 is a schematic sectional view showing a typical example of the heat ray-shielding multilayer glass of the present invention.

  In the present invention, “glass” means a transparent substrate in general, and may be a transparent plastic substrate in addition to a glass plate. Therefore, for example, the heat ray shielding glass means a transparent substrate provided with heat ray shielding properties.

  The heat ray shielding multi-layer glass 40 of the present invention includes a heat ray shielding glass 30, a glass plate 37 disposed so as to face the heat ray shielding glass 30 with a gap, and an adhesive (not shown) disposed on the outer periphery thereof. ), And a hollow layer 38 formed between the heat ray shielding glass 30 and the glass plate 37 by the spacer 39.

  The heat ray shielding glass 30 in the heat ray shielding multilayer glass 40 of the present invention will be described. In the heat ray shielding glass 30 shown in FIG. 1, an adhesive layer 22, a transparent plastic film 23, and a heat ray reflective layer 24 made of a conductive polymer are laminated and integrated in order on the surface of the glass plate 21. Usually, the heat ray shielding glass 30 forms a heat ray reflective layer 24 made of a conductive polymer on one surface of the transparent plastic film 23, and then the transparent plastic film 23 is opposite to the surface on which the above layer is formed. The surface is bonded to the glass plate 21 via the adhesive layer 22.

  Since the heat ray reflective layer 24 made of a conductive polymer is formed on the heat ray shielding glass 30, it is possible to effectively suppress the radiation of the heat rays and improve the heat insulation. This is thought to be because the plasma absorption wavelength due to free electrons of the conductive polymer is shorter than the radiation of an object near the ground temperature, and reflects electromagnetic waves having a wavelength higher than the plasma absorption wavelength.

  In the present invention, the surface resistance value of the heat ray reflective layer 24 made of a conductive polymer is 10000Ω / □ or less. With this surface resistance value, the free electron density is sufficiently high and sufficient heat insulation is obtained. The surface resistance value is preferably 1000Ω / □ or less, more preferably 300Ω / □ or less.

The heat ray reflective layer 24 is preferably formed on the outermost layer of the heat ray shielding glass 30 as shown in FIG. Although it is not preferable that there is another layer on the heat ray reflective layer 24, even a conductive (metal) thin film or a non-conductive organic resin hinders the radiation suppressing effect of the conductive polymer layer. If it is a thin film of an extent, it may be formed on the heat ray reflective layer 24. In this case, the surface resistance value of another layer is preferably 1 × 10 ⁶ Ω / □ or less, and the layer thickness is preferably 1 μm or less.

  In the present invention, the adhesive layer 22 and the transparent plastic film 23 may be omitted. The heat ray reflective layer 24 may be directly formed on the surface of the glass plate 21, or the adhesive layer 22 may be formed on the surface of the glass plate 21, and the heat ray reflective layer 24 may be formed on the surface. The heat ray shielding glass 30 is easy to manufacture and has improved impact resistance and penetration resistance. As shown in FIG. 1, the transparent plastic film 23 having the heat ray reflective layer 24 formed on the surface and the glass plate 21 are What was bonded together through the adhesive bond layer 22 is preferable.

  In the heat ray shielding multilayer glass 40 of the present invention, as shown, the heat ray shielding glass 30 is disposed so that the heat ray reflective layer 24 faces the glass plate 37. Thereby, the heat ray reflective layer 24 made of a conductive polymer can be protected from moisture such as rainwater, condensation, and moisture, and water resistance can be improved. Accordingly, it is possible to maintain the heat ray reflectivity (heat insulating property) and visible light permeability of the heat ray reflective layer 24 for a long period of time.

Below, the element which comprises the heat ray reflective glass 30 is demonstrated.
[Heat ray reflective layer]
The conductive polymer forming the heat ray reflective layer 24 is generally an organic polymer having a conjugated double bond as a basic skeleton, specifically, polythiophene, polypyrrole, polyaniline, polyacetylene, polyparaphenylene, polyfuran, polyfluorene. , Polyphenylene vinylene, derivatives thereof, and any one or a mixture of two or more conductive polymers selected from copolymers of monomers constituting them are preferable. Among these, polythiophene derivatives that are soluble or dispersible in water or other solvents and exhibit high conductivity and transparency are preferable. In particular, the following formula (I):

(In the formula, R ¹ and R ² each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or R ¹ and R ² together may be optionally substituted carbon. A polythiophene derivative containing a repeating unit represented by an alkylene group having 1 to 4 atoms and n represents an integer of 50 to 1000 is preferable.

In the formula (I), R ¹ and R ² are combined to form an alkylene group having 1 to 4 carbon atoms which may be used as a substituent, specifically, a methylene group substituted with an alkyl group, Examples thereof include groups that form ethylene-1,2 groups, propylene-1,3 groups, butene-1,4 groups optionally substituted with alkyl groups having 1 to 12 carbon atoms or phenyl groups.

As R1 and R2 in formula (I), preferably either a methyl group or an ethyl group, methylene ^{group R 1} and ^{R 2} form together an ethylene-1,2 radical or propylene-1,3 radical is there. Particularly preferred polythiophene derivatives include the following formula (II):

  (Wherein p represents an integer of 50 to 1000), that is, a polythiophene derivative having a poly (3,4-ethylenedioxythiophene) unit.

  The conductive polymer preferably further contains a dopant (electron donor). Preferred examples of the dopant include polystyrene sulfonic acid, polyacrylic acid, polymethacrylic acid, polymaleic acid, and polyvinyl sulfonic acid. In particular, polystyrene sulfonic acid is preferable. By these, the electroconductivity of a conductive polymer can be improved and the near-infrared shielding effect of the heat ray reflective layer 14 can be improved. The number average molecular weight Mn of the dopant is preferably 1,000 to 2,000,000, particularly preferably 2,000 to 500,000.

  Content of a dopant is 20-2000 mass parts normally with respect to 100 mass parts of conductive polymers, Preferably, it is 40-200 mass parts. For example, when the polythiophene derivative of the formula (II) is a conductive polymer and polystyrene sulfonic acid is used as a dopant, 100 to 200 parts by mass of polystyrene sulfonic acid is preferable with respect to 100 parts by mass of polythiophene, and particularly 120 to 180 parts by mass. Part is preferred.

  The heat ray reflective layer 24 made of a conductive polymer can be formed by a conventionally known method. For example, a coating solution in which a conductive polymer is dissolved or dispersed is applied to the surface of the transparent plastic film 23 or the glass plate 21 or the adhesive layer 22 by a bar coater method, a roll coater method, a curtain flow method, a spray method or the like. Coating is carried out using a method, and then dried to form. Solvents used in the coating liquid include water; alcohols such as methanol, ethanol and propanol; ketones such as acetophenone and methyl ethyl ketone; halogenated hydrocarbons such as carbon tetrachloride and fluorinated hydrocarbons; ethyl acetate and butyl acetate. Preferred examples include esters such as tetrahydrofuran, dioxane and diethyl ether; and amides such as N, N-dimethylacetamide, N, N-dimethylformamide and N-methylpyrrolidone. In particular, water and alcohols are preferable.

  The layer thickness of the heat ray reflective layer 24 made of a conductive polymer is preferably 10 to 3000 nm, more preferably 100 to 2000 nm, and particularly 150 to 1500 nm.

[Glass plate]
The glass plate 21 in the present invention may be a transparent substrate, for example, a glass plate such as green glass, silicate glass, inorganic glass plate, non-colored transparent glass plate, polyethylene terephthalate (PET), polyethylene naphthalate (PEN). ), A plastic substrate or film such as polyethylene butyrate or polymethyl methacrylate (PMMA) may be used. A glass plate is preferable in terms of weather resistance, impact resistance and the like. As for the thickness of a glass plate, about 1-20 mm is common.

[Transparent plastic film]
The transparent plastic film in the present invention is not particularly limited as long as it is a transparent plastic film (meaning “transparent to visible light”). Examples of plastic films include polyethylene terephthalate (PET) film, polyethylene naphthalate (PEN) film, polymethyl methacrylate (PMMA) film, polycarbonate (PC) film, polyethylene butyrate film, especially during processing. A PET film is preferred because of its high resistance to heat, solvent, bending and other loads, and high transparency. Moreover, in order to improve adhesiveness, the transparent plastic film surface may be subjected to adhesion treatment such as corona treatment, plasma treatment, flame treatment, primer layer coating treatment in advance, such as copolymer polyester resin and polyurethane resin. An easily adhesive layer such as a thermosetting resin may be provided. The thickness of the transparent plastic film is generally 1 μm to 10 mm, preferably 10 to 400 μm, and particularly preferably 20 to 200 μm.

[Adhesive layer]
The adhesive layer in the present invention comprises an ethylene-vinyl acetate copolymer (EVA), an ethylene-methyl acrylate copolymer, an ethylene- (meth) acrylic acid copolymer, an ethylene- (meth) ethyl acrylate copolymer. , Ethylene- (meth) acrylate methyl copolymer, metal ion cross-linked ethylene- (meth) acrylic acid copolymer, partially saponified ethylene-vinyl acetate copolymer, carboxylated ethylene-vinyl acetate copolymer, ethylene- ( Ethylene-based copolymers such as (meth) acrylic-maleic anhydride copolymer and ethylene-vinyl acetate- (meth) acrylate copolymer can be used ("(meth) acryl" means "acrylic or methacrylic" Is shown.) For the adhesive layer, polyvinyl butyral (PVB) resin, epoxy resin, phenol resin, silicon resin, polyester resin, urethane resin, rubber adhesive, thermoplastic elastomer such as SEBS and SBS, and the like can also be used. Among them, it is preferable to use EVA since it exhibits excellent adhesiveness, high long-term durability, and high transparency.

  EVA used for the adhesive layer has a vinyl acetate content of 23 to 38 parts by mass, particularly preferably 23 to 28 parts by mass with respect to 100 parts by mass of EVA. Thereby, the adhesive bond layer excellent in adhesiveness and transparency can be obtained. Moreover, it is preferable that the melt flow index (MFR) of EVA is 4.0-30.0 g / 10min, especially 8.0-18.0g / 10min. Pre-crimping becomes easy.

  When using an ethylene-type copolymer for an adhesive bond layer, it is preferable to contain an organic peroxide further. By crosslinking and curing with an organic peroxide, adjacent layers and a glass plate can be further joined and integrated. Any organic peroxide may be used in combination as long as it decomposes at a temperature of 100 ° C. or higher and generates radicals. The organic peroxide is generally selected in consideration of the film formation temperature, the adjustment conditions of the composition, the curing (bonding) temperature, the heat resistance of the adherend, and the storage stability. In particular, those having a decomposition temperature of 70 hours or more with a half-life of 10 hours are preferred.

  Examples of this organic peroxide include 2,5-dimethylhexane-2,5-dihydroperoxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexane-3-di- t-butyl peroxide, t-butylcumyl peroxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexane, dicumyl peroxide, α, α′-bis (t-butylperoxy) Isopropyl) benzene, n-butyl-4,4-bis (t-butylperoxy) valerate, 1,1-bis (t-butylperoxy) cyclohexane, 1,1-bis (t-butylperoxy) -3 , 3,5-trimethylcyclohexane, t-butyl peroxybenzoate, benzoyl peroxide, t-butyl peroxyacetate, methyl ethyl ketone pero Oxide, 2,5-dimethylhexyl-2,5-bisperoxybenzoate, butyl hydroperoxide, p-menthane hydroperoxide, p-chlorobenzoyl peroxide, hydroxyheptyl peroxide, chlorohexanone peroxide, octanoyl peroxide Oxide, decanoyl peroxide, lauroyl peroxide, cumyl peroxy octoate, succinic acid peroxide, acetyl peroxide, m-toluoyl peroxide, t-butyl peroxyisobutylene and 2,4-dichlorobenzoyl peroxide Can be mentioned.

  The adhesive layer preferably further contains a silane coupling agent as a crosslinking aid or adhesion improver.

  Examples of the crosslinking aid include polyfunctional compounds such as esters obtained by esterifying a plurality of acrylic acid or methacrylic acid with glycerin, trimethylolpropane, pentaerythritol, and the like, triallyl cyanurate, and triallyl isocyanurate.

  Examples of silane coupling agents include γ-chloropropylmethoxysilane, vinylethoxysilane, vinyltris (β-methoxyethoxy) silane, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, γ-glycidoxypropyltrimethoxy. Silane, γ-glycidoxypropyltriethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, vinyltrichlorosilane, γ-mercaptopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-β Mention may be made of-(aminoethyl) -γ-aminopropyltrimethoxysilane. These silane coupling agents may be used alone or in combination of two or more. Moreover, it is preferable that content of the said compound is 5 mass parts or less with respect to 100 mass parts of ethylene-type copolymers.

  The adhesive resin layer is used to improve or adjust various physical properties (optical properties such as mechanical strength, adhesiveness, and transparency, heat resistance, light resistance, crosslinking speed, etc.), especially to improve mechanical strength and light resistance. It preferably contains an acryloxy group-containing compound, a methacryloxy group-containing compound, an epoxy group-containing compound, a plasticizer, and an ultraviolet absorber. Examples of the ultraviolet absorber include benzophenone compounds, triazine compounds, benzoate compounds, and hindered amine compounds. From the viewpoint of suppressing yellowing, benzophenone compounds are preferred. The ultraviolet absorber is preferably used in an amount of 0.01 to 1.5 parts by mass (particularly 0.5 to 1.0 part by mass) with respect to 100 parts by mass of the ethylene copolymer.

  The thickness of the adhesive layer is preferably 100 to 2000 μm, particularly 400 to 1000 μm.

  In order to produce an adhesive layer containing an ethylene copolymer, for example, a composition containing an ethylene copolymer and an organic peroxide is formed by ordinary extrusion molding, calendar molding (calendering), or the like. For example, a method for obtaining a layered product can be used. The composition is preferably mixed by heating and kneading at a temperature of 40 to 90 ° C, particularly 60 to 80 ° C. The heating temperature during film formation is preferably a temperature at which the crosslinking agent does not react or hardly reacts. For example, it is preferable to set it as 40-90 degreeC, especially 50-80 degreeC. The adhesive layer may be formed directly on the surface of a transparent plastic film or glass plate, or may be formed separately using a film-like adhesive sheet.

In order to manufacture the heat ray shielding glass 30 according to the present invention, for example, the transparent plastic film 23 on which the heat ray reflective layer 24 is formed and the glass plate 21 are prepared, and the adhesive layer 22 (the heat ray reflection of the transparent plastic film as described above) is prepared. The transparent plastic film 24 on which the heat ray reflective layer 23 is formed and the glass plate 21 are laminated through a surface opposite to the surface on which the layer is formed or an adhesive sheet is laminated on the glass plate. The delaminated laminate was degassed and then pressed (preferably 1.0 × 10 ³ Pa-5.5) under heating (preferably at 40 to 200 ° C. for 1 to 120 minutes, particularly at 60 to 150 ° C. for 1 to 20 minutes). (Pressure of 0 × 10 ⁷ Pa) and bonding may be integrated.
These steps can be performed, for example, by a vacuum bag method, a nip roll method, or the like.

For example, when EVA is used for the adhesive layer 22, it is generally crosslinked at 100 to 150 ° C. (particularly around 130 ° C.) for 10 minutes to 1 hour. This is performed by degassing the laminated body, and pre-pressing at a temperature of, for example, 80 to 120 ° C., and performing a heat treatment at 100 to 150 ° C. (particularly around 130 ° C.) for 10 minutes to 1 hour. Cooling after crosslinking is generally performed at room temperature, and in particular, the faster the cooling, the better.

  Even when the transparent plastic film 23 is not used, the adhesive layer 22 can be provided on the glass plate 21 in order to improve the adhesion of the heat ray reflective layer 24 to the glass plate 21.

  As the hollow layer 38 in the heat ray shielding multilayer glass 40 of the present invention, an air layer, an inert gas layer, a reduced pressure layer, or the like can be used. According to these hollow layers, it is possible to improve the heat insulating properties required for the multilayer glass and to protect the heat ray shielding layer 24 from moisture such as rainwater and moisture. The air layer may use dry air by using a spacer containing a desiccant. The inert gas layer includes an inert gas such as krypton gas, argon gas, and xenon gas. The pressure of the reduced pressure layer is preferably 1.0 Pa or less, particularly 0.01 to 1.0 Pa. The thickness of the hollow layer is preferably 6 to 12 mm. The hollow layer 38 is preferably selected from any one of a dry air layer, an inert gas layer, and a reduced pressure layer. Thereby, the heat ray shielding layer 24 can be more appropriately protected from moisture, and the water resistance of the heat ray shielding multilayer glass 40 can be improved.

  The glass plate 37 in the heat ray shielding multilayer glass 40 of the present invention may be a transparent substrate similar to the glass plate 21. Float glass, template glass, ground glass with light diffusion function by surface treatment, meshed glass, lined glass, tempered glass, double tempered glass, low reflection glass, high transmission plate glass, ceramic printing glass, heat ray and UV absorption Various glasses such as special glass having a function can be appropriately selected and used. Moreover, about the composition of a glass plate, soda silicate glass, soda lime glass, borosilicate glass, aluminosilicate glass, various crystallized glass, etc. can be used.

  The heat ray shielding multilayer glass 40 of the present invention may have layers having various functions such as another heat ray shielding layer, a neon light-emitting absorption layer, and an ultraviolet absorption layer in addition to the heat ray reflection layer 24.

  The heat ray shielding layer is a layer containing a heat ray shielding agent other than the conductive polymer. The heat ray shielding agent is generally an inorganic material or an organic dye. For example, tungsten oxide and / or composite tungsten oxide, indium-tin oxide, tin oxide, antimony-tin oxide, phthalocyanine dye, metal complex dye, nickel dithiolene complex dye, cyanine dye, squarylium And dyes such as dyes, polymethine dyes, azomethine dyes, azo dyes, polyazo dyes, diimonium dyes, aminium dyes and anthraquinone dyes. These dyes can be used alone or in combination.

  The neon emission absorption layer (neon cut layer) is a layer containing a neon emission selective absorption dye. As selective absorption dyes for neon emission, porphyrin dyes, azaporphyrin dyes, cyanine dyes, squarylium dyes, anthraquinone dyes, phthalocyanine dyes, polymethine dyes, polyazo dyes, azurenium dyes, diphenylmethane dyes, A triphenylmethane type pigment | dye can be mentioned. Such a selective absorption dye is required to have a selective absorption of neon emission near 585 nm and a small absorption at other visible light wavelengths. Therefore, the absorption maximum wavelength is 560 to 610 nm, and the absorption spectrum half width is What is 40 nm or less is preferable.

  The ultraviolet absorbing layer is a layer containing an ultraviolet absorber, and examples of the ultraviolet absorber include benzophenone compounds, benzotriazole compounds, triazine compounds, benzoate compounds, hindered amine compounds, salicylic acid compounds, and cyanoacrylate compounds. Compounds and the like can be used.

These layers may be formed as separate layers according to the properties (solubility, reactivity, etc.) of each compound, or may be formed as the same layer by mixing each compound. In addition, a coloring pigment, an antioxidant, and the like may be further added to these layers as long as the optical properties are not greatly affected.
Further, these layers may be formed on the heat ray shielding glass 30 side of the heat ray shielding multilayer glass 40, for example, on the lower layer or the upper layer (preferably the lower layer) of the heat ray reflective layer 24, or on the glass plate 37 side. May be.

  In particular, in order to prevent the conductive polymer from being deteriorated by ultraviolet rays, it is preferable that the ultraviolet absorbing layer is formed on the side where the sunlight is irradiated (outdoor) with respect to the heat ray shielding layer 24. That is, when the heat ray shielding glass 30 is disposed on the outdoor side, the ultraviolet ray absorbing layer is on the lower layer of the heat ray reflecting layer 24 in the heat ray shielding glass 30 or the surface opposite to the surface on which the heat ray reflecting layer 24 of the glass plate 21 is formed. Preferably it is formed. Moreover, when the glass plate 37 is arrange | positioned on the outdoor side, it is preferable that the ultraviolet absorption layer is formed in the upper layer of the heat ray shielding layer 24 or the surface of the glass plate 37. FIG.

  The shape of the heat ray shielding multilayer glass of the present invention can be various shapes such as a rectangular shape, a round shape, and a rhombus shape depending on applications. As for the application of heat ray-shielding double-glazed glass, various kinds of equipment such as window glass for buildings and vehicles (automobiles, railway vehicles, ships) or equipment such as plasma displays, refrigerators, heat insulation devices, etc. It can be used for various applications such as doors and walls.

  When the heat ray shielding multilayer glass of the present invention is used for a building or a vehicle in a warm region such as a relatively low latitude region, the glass plate is disposed on the indoor side and the heat ray shielding glass is disposed on the outdoor side. It is preferable. This is because sunlight and the near infrared rays irradiated from the outside can be effectively shielded. On the other hand, when the heat ray shielding multilayer glass of the present invention is used in a cold region such as a region having a relatively high latitude, it is preferable that the glass plate is disposed on the outdoor side and the heat ray shielding glass is disposed on the indoor side. This is because infrared rays such as heating emitted from the room are reflected and not escaped (heat insulation), and the heating efficiency can be improved. Since the heat ray shielding double-glazed glass of the present invention is excellent in heat insulation, it can be used more effectively in cold regions.

Hereinafter, the present invention will be described in more detail with reference to examples.
1. Comparison of double-layer glass and single-layer glass (A) Production of heat ray shielding glass (single-layer glass) (Comparative Example 1)
(1) Formation of heat ray reflective layer An aqueous dispersion (solid content: 1.2% by mass) of a mixture of polythiophene derivative A and polystyrene sulfonic acid (1: 2.5 parts by mass) on a PET film (thickness 100 μm) ( Clevios FE (manufactured by HC Starck) was applied using a bar coater and dried at 120 ° C. for 3 minutes to form a heat ray reflective layer (thickness 150 nm) on the PET film.
(2) Production of Adhesive Layer A composition having the following composition was rolled into a sheet by a calendering method to obtain an adhesive layer (thickness 0.4 mm). The blend was kneaded at 80 ° C. for 15 minutes, the calender roll temperature was 80 ° C., and the processing speed was 5 m / min.
(Combination)
EVA (content of vinyl acetate with respect to 100 parts by mass of EVA: 25 parts by mass; Ultrasen 635 (manufactured by Tosoh Corporation)): 100 parts by mass,
Organic peroxide (tert-butyl peroxy 2-ethylhexyl carbonate; Trigonox 117 (manufactured by Kayaku Akzo): 2.5 parts by mass,
Cross-linking assistant (triallyl isocyanurate; TAIC (registered trademark) (manufactured by Nippon Kasei Co., Ltd.)): 2 parts by mass,
Silane coupling agent (γ-methacryloxypropyltrimethoxysilane; KBM503 (manufactured by Shin-Etsu Chemical Co., Ltd.)): 0.5 part by mass UV absorber: (Ubinal 3049 (manufactured by BASF)): 0.5 part by mass (3) Production of heat ray shielding glass On a glass plate (thickness 3 mm), an adhesive layer and a heat ray reflective layer formed on a PET film were laminated in this order. The obtained laminate was temporarily pressed by heating at 100 ° C. for 30 minutes, and then heated in an autoclave for 30 minutes under conditions of a pressure of 13 × 10 ⁵ Pa and a temperature of 140 ° C. Thereby, the adhesive layer was cured to obtain a heat ray shielding glass in which the glass plate and the transparent plastic film were bonded and integrated.
(Comparative Example 2)
A heat ray shielding glass was obtained in the same manner as in Comparative Example 1 except that the polythiophene derivative A was changed to polythiophene derivative B (SEPLEGYDA OC-X109 (manufactured by Shin-Etsu Polymer Co., Ltd.)).
(Comparative Example 3)
A heat ray shielding glass was obtained in the same manner as in Comparative Example 1 except that the polythiophene derivative A was changed to a polythiophene derivative C (SEPLEGYDA OC-AE23 (manufactured by Shin-Etsu Polymer Co., Ltd.)).

(B) Production of double-glazed glass (Example 1)
The glass plate (thickness 3 mm) and the heat ray shielding glass produced in Comparative Example 1 were arranged to face each other through frame-shaped aluminum spacers arranged on the peripheral edge portions thereof, and these were bonded with butyl rubber. At this time, the surface on which the heat ray reflective layer of the heat ray shielding glass was formed was set to the air layer side formed by the spacer. The thickness of the air layer was 6 mm.
(Example 2)
A multilayer glass was produced in the same manner as in Example 1 except that the heat ray shielding glass was produced in Comparative Example 2.
(Example 3)
A multilayer glass was produced in the same manner as in Example 1 except that the heat ray shielding glass was produced in Comparative Example 3.

(C) Evaluation method Each glass sample was wet-heat treated for 500 hours in an atmosphere at a temperature of 85 ° C. and a humidity of 85% RH, and the haze value (%) before and after the treatment was determined using Nippon Denshoku Industries Co., Ltd. Haze Meter NDH2000. Measured.

(D) Evaluation results Table 1 shows the evaluation results of the respective glass samples.

  As shown in Table 1, in the case of Comparative Examples 1 to 3 of the single-layer glass, it was confirmed that any polythiophene derivative increased the haze value after wet heat treatment and the water resistance was low. On the other hand, in Examples 1 to 3 of the multi-layer glass, it was confirmed that any polythiophene derivative had no change in the haze value before and after the wet heat treatment, and the water resistance was improved.

2. Evaluation of double-glazed glass (A) Preparation of double-glazed glass (Example 4)
(1) Formation of heat ray reflective layer An aqueous dispersion (solid) of a mixture of poly (3,4-ethylenedioxythiophene) and polystyrenesulfonic acid (1: 2.5 parts by mass) on a PET film (thickness: 100 μm) 1.2 mass%) was applied using a bar coater and dried at 120 ° C. for 3 minutes to form a heat ray reflective layer (thickness 150 nm) on the PET film.
(2) Production of adhesive layer An adhesive layer was produced in the same manner as in Comparative Example 1 (2).
(3) Preparation of heat ray shielding glass Heat ray shielding glass was produced similarly to the comparative example 1 (3).
(4) Production of Multi-layer Glass A multi-layer glass was produced in the same manner as in Example 1.

(Example 5)
A multilayer glass was prepared in the same manner as in Example 4 except that the thickness of the heat ray reflective layer was 450 nm.

(Comparative Example 4)
A multilayer glass was produced in the same manner as in Example 1 using two glass plates (thickness 3 mm).

(Comparative Example 5)
(1) Formation of heat ray reflective layer On a PET film (thickness 100 μm), a polyaniline methanol dispersion (solid content 1% by mass) was applied using a bar coater and dried at 120 ° C. for 3 minutes. A heat ray reflective layer (thickness 150 nm) was formed.
(2) Production of adhesive layer An adhesive layer was produced in the same manner as in Comparative Example 1 (2).
(3) Production of heat ray shielding glass A heat ray shielding glass was produced in the same manner as in Comparative Example 1 (3).
(4) Production of Multi-layer Glass A multi-layer glass was produced in the same manner as in Example 1.

(Comparative Example 6)
(1) Production of heat ray shielding glass Using an in-line type DC sputtering device, an indium tin oxide (ITO) film, a silver film, an ITO film, a silver film, an ITO film on a glass plate (thickness 3 mm) from the glass plate side. By forming a heat ray reflective film including the films in this order, a heat ray shielding glass was obtained. Sputtering was performed with indium tin oxide by introducing argon and oxygen at a flow ratio of 98:10 at a discharge current of 6 A, and with silver by introducing only argon and at a discharge current of 0.9 A.
(2) Production of Multi-layer Glass A multi-layer glass was produced in the same manner as in Example 1 using the glass plate (thickness 3 mm) and the heat ray shielding glass produced in (1).

(B) Evaluation method (1) Surface resistance value The surface resistance value of each heat ray shielding glass was measured using a resistivity meter Loresta GP (manufactured by Mitsubishi Chemical Corporation).
(2) Heat flow rate Measured according to JIS R3107.
(3) Weather resistance Each glass sample was left in an atmosphere of a temperature of 85 ° C. and a humidity of 85% RH for 1000 hours to evaluate the appearance. The case where there was no change in appearance was marked with ◯, and the case where there was a change in appearance such as corrosion was marked as x.

(C) Evaluation results Table 2 shows the evaluation results of the respective glass samples.

As shown in Table 2, it is shown that the double-glazed glass of Examples 4 and 5 has a low heat transmissivity and low heat ray radiation (high heat insulation) compared to Comparative Example 4 without a heat ray reflective layer. It was. Even if there was a heat ray reflective layer made of a conductive polymer, Comparative Example 5 having a surface resistance value of 1 × 10 ⁶ Ω / □ had a high heat transmissivity and a sufficient heat insulating property could not be obtained. In addition, the multilayer glass having a heat ray reflective layer of the ITO / Ag film of Comparative Example 6 has low weather resistance, and the multilayer glass of Examples 1 and 2 was superior in this respect.

  In addition, this invention is not limited to said embodiment and Example, A various deformation | transformation is possible within the range of the summary of invention.

  It is possible to provide heat ray shielding glass at a low cost that can reduce the air conditioning load of buildings such as office buildings and buses, passenger cars, trains, and other vehicles and railways over a long period of time.

30: Heat ray shielding glass 21, 37: Glass plate 22: Adhesive layer 23: Transparent plastic film 24: Heat ray reflective layer 38: Hollow layer 39: Spacer 40: Multi-layer glass

Claims (5)

A heat ray-shielding glass having a glass plate and a heat ray reflective layer made of a conductive polymer provided on the surface of the glass plate and another glass plate with a gap therebetween, and the heat ray reflective layer is attached to the other glass plate. It is arranged so as to face, and the hollow layer is formed by the gap, and the surface resistance of the heat ray reflective layer is, 10000 ohms / □ Ri der below,
The heat ray shielding multilayer glass, wherein the heat ray reflective layer is located on the uppermost layer of the heat ray shielding glass. The conductive polymer has the following formula (I):

(In the formula, R ¹ and R ² each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or R ¹ and R ² together may be optionally substituted carbon. The heat ray shielding multilayer glass according to claim 1, which is a polythiophene derivative containing a repeating unit represented by an alkylene group having 1 to 4 atoms, and n represents an integer of 50 to 1000.   The heat ray shielding multilayer glass according to claim 1 or 2, wherein the heat ray reflective layer has a thickness of 10 to 3000 nm.   The heat ray shielding according to any one of claims 1 to 3, wherein the heat ray shielding glass is obtained by bonding a transparent plastic film having a heat ray reflective layer formed on a surface thereof and a glass plate via an adhesive layer. Double layer glass.   The heat ray shielding multilayer glass according to claim 4, wherein the adhesive layer contains an ethylene-vinyl acetate copolymer.

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