JP4954438B2 - Solar radiation shielding laminated structure - Google Patents

Description

  The present invention relates to a solar-shielding laminated structure used as a safety glass for vehicles such as automobiles, window glass for buildings, etc., for example, having a haze value of 0.4% or less, good adhesion, and high. The present invention relates to a solar shading laminated structure having a good solar shading function even under conditions of visible light transmittance.

  Conventionally, as safety glass for automobiles and the like, a laminated glass is formed by sandwiching an intervening layer having a solar radiation shielding function between two sheet glasses, and the solar energy entering from the laminated glass is cut off to reduce the cooling load and the heat of the person. The thing for the purpose of the reduction of a feeling is proposed.

  For example, in Patent Document 1, Sn, Ti, Si, Zn, Zr, Fe, Al, Cr, Co, Ce, In, Ni, Ag, Cu, Pt, Mn, and Ta are provided between at least two sheet glasses. , W, V, Mo metal, oxides, nitrides, sulfides, Sb and F dopes, or composites thereof are dispersed in a vinyl resin, and the intermediate film is formed as the intervening layer. A laminated glass is disclosed.

  In Patent Document 2, an intermediate film composed of three layers is provided between at least two transparent glass plates, and the intermediate film of the second layer is formed of Sn, Ti, Si, Zn, Zr, Fe, Al. , Cr, Co, In, Ni, Ag, Cu, Pt, Mn, Ta, W, V, and Mo metals, oxides, nitrides, sulfides, Sb and F dopants, and composites thereof. There has also been proposed a laminated glass comprising a layer dispersed in a vinyl-based resin and having an interlayer film of the first layer and the third layer made of a resin layer.

  By the way, in the conventional laminated glass described in Patent Documents 1 and 2, solar shielding components such as tin-containing indium oxide (ITO) fine particles are dispersed in a high concentration in the vinyl resin which is the resin component of the intermediate film. In the case where the laminated glass is formed by dispersing ITO having a blending amount of about 0.4% or less, the visible light transmittance is low. There was a problem that it was difficult to obtain a laminated glass having a solar transmittance of less than 40% under conditions of around 72%.

Furthermore, the tin-containing indium oxide (ITO) fine particles having a blending amount having a haze value of about 0.4% or less are dispersed, and the solar radiation transmittance is about 42 to 46% under the condition that the visible light transmittance is about 72%. Although it is possible to produce laminated glass with a solar transmittance of 40% or more, the ITO fine particles dispersed in the interlayer film are expensive materials, so the solar light transmission under conditions where the visible light transmittance is around 72% Even if it is a laminated glass with a rate of about 40% or more, there is a problem that its manufacturing cost increases.
JP-A-8-259279 (paragraph number 0012) JP-A-10-297945 (paragraph number 0018) JP-A-7-69632 (Claims 1 and 2)

  The present invention has been made paying attention to such problems, and the problem is that the solar transmittance under a condition where the haze value is 0.4% or less and the visible light transmittance is around 72% is 42. An object of the present invention is to provide a solar radiation shielding laminated structure that can be manufactured at a low cost for a solar radiation shielding laminated structure of about ~ 46%.

  Thus, as a result of intensive studies by the present inventors to solve the above-mentioned problems, unlike vinyl resins, alkyl silicates whose haze value is unlikely to exceed 0.4 even when the solar radiation shielding component is dispersed at a high concentration. Alternatively, an acrylic resin was discovered, and a solar radiation shielding component having an excellent solar radiation shielding function was found. The present invention has been completed based on such technical findings.

That is, the invention according to claim 1
Assuming a solar radiation shielding laminated structure in which an intervening layer having a solar radiation shielding function is interposed between at least two transparent glass or plastic plates,
The intervening layer is constituted by the solar radiation shielding layer of the solar radiation shielding film in which the ultraviolet radiation curable resin made of acrylic resin and the solar radiation shielding layer containing hexaboride fine particles are formed on one side of the ductile film substrate, and the one plate The solar radiation shielding layer of the solar radiation shielding film is placed in contact with the mating surface side of the sheet-like body, and a vinyl-based resin is placed between the mating surface side of the other plate-like body and the ductile film substrate side of the solar radiation shielding film. An intermediate film as a main component is arranged, and the visible light transmittance is 72%, the solar transmittance is 42 to 46%, and the haze value is 0.4% or less.
The invention according to claim 2
Assuming a solar radiation shielding laminated structure in which an intervening layer having a solar radiation shielding function is interposed between at least two transparent glass or plastic plates,
An intervening layer is constituted by the above-mentioned solar shading layer of an intermediate film mainly composed of a vinyl resin in which a UV-curing resin made of acrylic resin and a solar shading layer containing hexaboride fine particles are formed on one side. The solar radiation shielding layer of the intermediate film is in contact with the mating surface side of one plate, and the opposite side of the intermediate film is in contact with the mating surface of the other plate, and the visible light transmittance is Is 75%, the solar transmittance is 42 to 46%, and the haze value is 0.4% or less.

According to the solar radiation shielding laminated structure according to the inventions of claims 1 and 2 ,
In addition to an intermediate film mainly composed of a vinyl resin and adhering at least two plates, a solar radiation shielding layer containing a UV curable resin made of an acrylic resin and hexaboride fine particles and acting as the intermediate layer is provided. It is incorporated.

Further, even if the solar radiation shielding component is dispersed at a high concentration in the UV curable resin made of the acrylic resin , the haze value of the solar radiation shielding layer is difficult to exceed 0.4%, and further, the solar radiation shielding layer is dispersed in the solar radiation shielding layer. The boride fine particles have an excellent solar shading function as compared with conventional solar shading components such as ITO, so that it is possible to reduce the blending amount of the solar shading components and have the above structure. Has adhesive properties.

Therefore, by constituting the solar shading component with hexaboride fine particles , the solar shading transmittance is about 42 to 46% under the condition that the haze value is 0.4% or less and the visible light transmittance is around 72%. The laminated structure can be manufactured at low cost.

  Hereinafter, the present invention will be described in detail.

  First, the first solar shading laminated structure according to the present invention includes a pair of transparent glass or plastic plate-like bodies 1 and 5 as shown in FIG. 1, a solar shading film 10 and an intermediate film disposed therebetween. 4 and the main part are comprised.

The solar shading film 10 is composed of a ductile film substrate 3 and a solar shading layer 2 containing UV curable resin and hexaboride fine particles made of acrylic resin formed on one side of the film. The solar radiation shielding layer 2 is disposed so as to contact the mating surface side of one plate-like body 1, the mating surface side of the other plate-like body 5, and the ductile film substrate 3 side of the solar radiation shielding film 10. The intermediate film 4 containing a vinyl resin as a main component is disposed between them.

On the other hand, as shown in FIG. 2, the second solar radiation shielding laminated structure according to the present invention includes a pair of transparent glass or plastic plate-like bodies 1 and 5, an intermediate film 4 disposed therebetween, and the intermediate film. The solar shading layer 2 formed on one side of the main part of the solar shading layer 2 comprises a main part thereof, and the solar shading shielding layer 2 includes a UV curable resin made of acrylic resin and hexaboride fine particles. To do.

  And the transparent glass as the plate-shaped bodies 1 and 5 in the 1st and 2nd solar radiation shielding laminated structure which concerns on this invention is suitably selected by a use. For example, inorganic glass, organic glass or composite glass thereof, especially inorganic transparent clear or colored glass produced by the so-called float method, tempered glass or similar glass, with a coating film such as a primer or various functional films Glass etc. are mentioned. Preferably, there are green glass and bronze glass, and further, gray glass, blue glass, and the like can be used. The plate thickness of the plate-like body is arbitrary and not particularly limited, but is usually about 1.0 mm or more and about 12 mm or less, and particularly for automobiles, preferably about 1.5 mm or more and about 3.0 mm or less. It is more preferably about 0.0 mm or more and 2.5 mm or less.

  Examples of the plastic as the plate-like bodies 1 and 5 include polycarbonate resin and polymethyl methacrylate resin. In addition, the plate | board thickness of a plastic plate-shaped object is also arbitrary and is set suitably according to a use.

Next, as the ductile film substrate 3 of the first solar radiation shielding laminated structure according to the present invention, for example, a film substrate made of a polyester resin may be mentioned. In addition, the surface of the film substrate may be subjected to surface treatment such as corona treatment, plasma treatment, flame treatment, primer layer coating treatment, etc., for the purpose of improving adhesiveness with UV curable resin made of acrylic resin. .

  In addition, as an intermediate film mainly composed of a vinyl resin in the first and second solar radiation shielding laminated structures according to the present invention, any intermediate film for a conventional laminated glass is applicable. It is not particularly limited as long as it can be an interlayer film that can match the quality of the laminated glass with the needs. For example, polyvinyl acetal represented by polyvinyl butyral, polyvinyl chloride, vinyl chloride-ethylene copolymer, vinyl chloride-ethylene-glycidyl methacrylate copolymer, vinyl chloride-ethylene-glycidyl acrylate copolymer, vinyl chloride-glycidyl methacrylate Examples include copolymers, vinyl chloride-glycidyl acrylate copolymers, polyvinylidene chloride, vinylidene chloride-acrylonitrile copolymers, polyvinyl acetate-ethylene acetate copolymers, polyvinyl acetal-polyvinyl butyral mixtures, and the like. Further, a plasticizer may be added to the vinyl resin. Examples of the plasticizer include dioctyl phthalate, dibutyl phthalate, diisobutyl phthalate, adipic acid-di-2-ethylhexyl, diisodecyl adipate, epoxy fatty acid monoester, Examples include triethylene glycol-di-2-ethylbutyrate, triethylene glycol-di-2-ethylhexanoate, dihexyl adipate, dibutyl sebacate, dibutyl sebacate and the like.

  The intermediate film surface on the side in contact with the transparent glass or plastic plate surface is preferably embossed from the viewpoint of adhesiveness. In the intermediate film, in order to further enhance the solar shading performance, hexaboride fine particles alone or hexaboride fine particles and tin-containing indium oxide fine particles and / or antimony-containing tin oxide are used within a range in which the haze value does not increase. Fine particles may be added. Further, an ultraviolet absorber, an antioxidant, an antistatic agent, a heat stabilizer, a lubricant, a filler, a coloring agent, an adhesion adjusting agent, and the like may be added depending on applications.

Next, the solar radiation shielding layer 2 provided on one side of the ductile film substrate 3 or the intermediate film 4 includes UV curable resin and hexaboride fine particles made of acrylic resin as described above.

The hexaboride fine particles are preferably fine particles having a specific surface area of 10 m ² / g or more (corresponding to an average particle size of about 127 nm or less) . This is because if the specific surface area of the fine particles deviates from the above characteristics, desired optical characteristics may not be obtained . The above specific surface area, is measured by a nitrogen gas adsorption method using a Carlo Erba Co. apparatus.

Next, the above hexaboride fine particles used in the present invention have a higher solar shielding effect as the crystal completeness is higher, but the crystallinity is low and a broad diffraction peak is generated by X-ray diffraction. However, there is no particular limitation as long as the basic bonds inside the fine particles are composed of bonds between each metal and boron. Typical examples are LaB ₆ , CeB ₆ , PrB ₆ , NdB ₆ , GdB ₆ , TbB ₆ , DyB ₆ , HoB ₆ , YB ₆ , SmB ₆ , EuB ₆ , ErB ₆ , TmB ₆ , YbB ₆ , LuB _6. , (La, Ce) B ₆ , SrB ₆ , CaB _{6 and the} like, but LaB ₆ , CeB ₆ , PrB ₆ , NdB ₆ and GdB ₆ are particularly preferable. Although the surface of the hexaboride fine particles is preferably not oxidized, it is usually slightly oxidized, and it is inevitable that the surface is oxidized in the fine particle dispersion process to some extent. However, even in that case, it does not affect the effectiveness of the solar radiation shielding effect.

  In order to use the hexaboride particles more stably, it is preferable to coat the surface of the hexaboride fine particles. This coating compound is a compound of one or more elements selected from Si, Ti, Al, Zr, and any of the above compounds such as a compound containing an alkoxy group in the molecule or a hydrolysis polymer thereof, or sodium silicate. Examples thereof include sodium salts and potassium salts containing these elements, and mixtures thereof. In particular, as the Si compound, alkoxysilane, chlorosilane, silazane, or a hydrolysis polymer thereof is preferable, and those commercially available as surface treatment agents can be used.

  In the alkoxysilane, the alkoxy group forms a covalent bond with the hexaboride particles on the particle surface, thereby covering the particle surface and improving water resistance. Typical examples include tetramethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, diphenyldimethoxysilane, tetraethoxysilane, methyltriethoxysilane, dimethyldiethoxysilane, phenyltriethoxysilane, diphenyldiethoxy. Examples include silane, hexyltrimethoxysilane, hexyltriethoxysilane, decyltriethoxysilane, decyltrimethoxysilane, triuropropyltrimethoxysilane, heptadecatrifluorodecyltrimethoxysilane, and the like.

  In the chlorosilane, the chloro group forms a covalent bond with the hexaboride particles on the particle surface, thereby covering the particle surface and improving the water resistance. Typical examples include methyltrichlorosilane, methyldichlorosilane, dimethyldichlorosilane, trimethylchlorosilane, phenyltrichlorosilane, diphenyldichlorosilane, trifluoropropyltrichlorosilane, heptadecafluorodecyltrichlorosilane, and the like.

  The silazane is highly reactive with the hexaboride particles, and can be covalently bonded to the hexaboride particles on the particle surface, and the particle surface can be covered with silazane. Further, silazane is lipophilic and has a small molecular structure, so that it can cover the particle surface densely, and the outermost contour is hydrophobic, which is effective for improving water resistance. Specific examples include hexamethyldisilazane, cyclic silazane, N, N-bis (trimethylsilyl) urea, N-trimethylsilylacetamide, dimethyltrimethylsilylamine, diethyltrimethylsilylamine, trimethylsilylimidazole, N-trimethylsilylphenylurea and the like.

  The surface treatment of hexaboride particles is not particularly limited as long as the particle surface can be coated with a coating compound such as a Si compound. For example, the coating compound may act directly on the hexaboride particles to coat the surface. In particular, there is a wet method as a method for efficiently covering the particle surface. In this method, hexaboride particles are dispersed in a liquid, and one or more coating compounds such as an alkoxysilane surface treatment agent and sodium silicate are added and mixed therewith. A coating compound such as an alkoxysilane surface treatment agent or a sodium salt efficiently covers the particle surface in a liquid and can easily provide coated hexaboride particles having improved water resistance.

  Further, if hexaboride particles are aggregated, a portion where the coating is not sufficiently performed remains, and an uncoated portion appears when the aggregation is released in a later process, and thus water resistance may not be sufficiently obtained. In order to prevent the uncoated portion from remaining, it is preferable to break up the aggregation of the particles in the liquid by means such as ultrasonic irradiation or a stirring mill.

In addition, the hexaboride fine particles are powders colored in gray-black, brown-black, green-black, etc., but the particle size is sufficiently smaller than the visible light wavelength and visible in the solar-shielding layer when dispersed in the solar-shielding layer. Although light transmittance occurs, the infrared light shielding ability can be kept sufficiently strong. The reason for this is not known in detail, but the amount of free electrons in these fine particles is large, and the absorption energy of indirect interband transition due to free electrons inside and on the surface of the fine particles is in the vicinity of visible to near infrared. Therefore, it is considered that heat rays in this wavelength region are selectively reflected and absorbed. According to experiments, in a film in which hexaboride fine particles have a specific surface area of 10 m ² / g or more and are uniformly dispersed, the transmittance has a maximum value between wavelengths of 400 nm and 700 nm, and has a wavelength of 700 nm to 1800 nm. It is observed that there is a minimum value in between, and the difference between the maximum value and the minimum value of these transmittances is 15 points or more. Considering that the visible light wavelength is 380 nm to 780 nm and the visibility is a bell-shaped peak with a peak near 550 nm, such a film effectively transmits visible light and effectively reflects or absorbs other heat rays. To do.

Hand, Suzu含 organic indium oxide fine particles, almost no reflection and absorption of light in the visible light region, a large reflection or absorption from plasma resonance 1000nm or more regions. These transmission profiles tend to decrease toward the longer wavelength side in the near infrared region.

  Further, the transmission profile of the antimony-containing tin oxide fine particles decreases as it goes to the longer wavelength side in the near-infrared region, similar to the tin-containing indium oxide fine particles, but the shielding properties in the near-infrared region are compared with the tin-containing indium oxide fine particles. And inferior.

As described above, the transmission profile of the hexaboride fine particles has a minimum value between wavelengths of 700 nm and 1800 nm, specifically, a minimum value near 1000 nm, and tends to gradually increase on the longer wavelength side. Show. For this reason, by using hexaboride fine particles, it becomes possible to shield sunlight rays in the near-infrared region without reducing visible light transmittance, and use tin-containing indium oxide fine particles or antimony-containing tin oxide. It is possible to improve the solar radiation shielding characteristics than to do.

In addition, the solar shading ability per unit weight of the hexaboride fine particles is very high, and exhibits its effect at a use amount of 1/10 or less compared with tin-containing indium oxide fine particles and antimony-containing tin oxide fine particles . Only the solar shading property can be further improved while maintaining a certain visible light transmittance, and the cost can be reduced. Further, since the amount of all fine particles used can be greatly reduced, it is possible to improve the wear strength and weather resistance of the solar radiation shielding layer. In addition, since the hexaboride fine particles absorb in the visible light region when the amount used is increased, the absorption in the visible light region can be controlled freely by controlling the amount of addition, and application to brightness adjustment, privacy protection, etc. Is also possible.

In order to obtain a solar radiation shielding laminated structure having more excellent optical characteristics, the powder color L * in the L * a * b * color system of hexaboride fine particles is 30 to 51, and a * is −. It is desirable to satisfy the conditions that 5 to 10 and b * are −10 to 2.

Next, the method for forming the solar radiation shielding layer on one side of the ductile film substrate or intermediate film is optional, but the binder component and hexaboride fine particles of UV curable resin made of acrylic resin are dispersed in the solvent. The method using the coating solution for forming the solar radiation shielding layer is exemplified.

The method for dispersing the hexaboride fine particles in the solvent is arbitrary as long as the fine particles are uniformly dispersed in the solvent, and examples thereof include a bead mill, a ball mill, a sand mill, and an ultrasonic dispersion method. The solvent is not particularly limited. For example, alcohols such as ethanol, propanol, butanol, isopropyl alcohol, isobutyl alcohol and diacetone alcohol, ethers such as methyl ether, ethyl ether and propyl ether, and esters Various organic solvents such as ketones such as acetone, methyl ethyl ketone, diethyl ketone, cyclohexanone, and isobutyl ketone, and the pH may be adjusted by adding an acid or an alkali as necessary. Furthermore, various surfactants, coupling agents, and the like may be added to improve the dispersion stability of the fine particles in the coating solution. Examples of the method for applying the solar shading layer forming coating solution on one side of the ductile film substrate or intermediate film include, for example, spin coating, bar coating, spray coating, dip coating, screen printing, roll coating. Any method may be used as long as it can apply the coating solution for forming the solar shading layer flatly, thinly and uniformly, such as a method and a flow coating.

  An adhesive layer may be interposed between the mating surface side of one plate and the solar radiation shielding layer as necessary. Examples of the material constituting the adhesive layer include vinyl chloride-vinyl acetate copolymer, ethylene-vinyl acetate copolymer, polyamide resin, urethane resin, ethylene-vinyl acetate-epoxy terpolymer, ethylene-vinyl acetate- Examples thereof include vinyl alcohol terpolymer, ethylene-vinyl acetate-acrylate terpolymer, and polyvinyl acetal resin represented by polyvinyl butyral. Further, the surface of the adhesive layer may be treated with a silane or titanate coupling agent.

  Examples of the present invention will be specifically described below, but the present invention is not limited to the following examples.

  Further, the powder color (light source D65), the visible light transmittance and the solar transmittance of the obtained laminated structure were measured using a spectrophotometer “U-4000” manufactured by Hitachi, Ltd., and The haze value is measured using “HR-200” manufactured by Murakami Color Research Laboratory Co., Ltd. In film evaluation, the film was formed with three types of bar coaters with different wire diameters, and the visible light transmittance, solar transmittance, and haze value of three types of films with different film thicknesses were measured. The solar radiation transmittance and haze value when the visible light transmittance is 72% or the visible light transmittance is 75% are determined from the three-point plot of the film. In particular, assuming an automobile use, the solar radiation transmittance was 50% or less and the haze value was 0.4% or less. Furthermore, the adhesion between the plate glass surface and the interlayer film was evaluated by the following Pummel test.

[Panmel test]
After holding the laminated structure for 16 hours under the condition of −18 ° C. ± 0.6 ° C., it is put on a hammer (head part weight is 1 pound) crushing tester, and the particle size of the deposited glass is 6 mm or less at maximum. Grind until

  Next, the broken glass piece was shaken off, and the degree of exposure of the intermediate film was ranked from 0 to 8 to evaluate the adhesion between the plate glass and the intermediate film.

  The lower the degree of exposure, the larger the Pummel value and the lower the penetration resistance, but the range of 3 to 7 is desirable.

After mixing 20% by weight of LaB ₆ fine particles with a specific surface area of 19.7 m ² / g, 7% by weight of a polymeric dispersant and 73% by weight of isobutyl alcohol, and filling the container together with ZrO ₂ beads having a diameter of 0.3 mm, 6 A lanthanum hexaboride fine particle dispersion was prepared by subjecting to a bead mill dispersion treatment for a period of time (liquid A).

Next, a UV curable resin (acrylic resin trade name grade UV3701 manufactured by Toa Gosei Co., Ltd.) and ethanol as a diluent are added to the prepared liquid A, and a solar radiation shielding layer having a LaB ₆ fine particle concentration of 0.2% by weight. A forming coating solution was prepared.

  Next, the coating solution for forming the solar shading layer is applied on one side of a ductile polyester film (thickness 50 μm) with a bar coater, dried, and then irradiated with a high-pressure mercury lamp at 70 ° C. for 1 minute. A shielding layer was formed.

The solar-shielding layer side of the ductile polyester film is disposed so as to be in contact with the mating surface of the green glass having a dimension of 100 mm × 100 mm × about 2 mm thickness, and the ductile polyester film side and the dimension of 100 mm × 100 mm × about 2 mm thickness A polyvinyl butyral resin for interlayer film having a thickness of 0.76 mm is interposed between the green glass and the other glass glass, which is temporarily mounted by heating to 80 ° C. and then fully mounted by autoclave at 140 ° C. under conditions of 14 kg / cm ^2. The laminated structure A according to Example 1 was manufactured.

  As shown in Table 1 below, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 42.3% and 0.2%, respectively, and the Pummel value was 5 and good. .

  A laminated structure B according to Example 2 was produced in the same manner as in Example 1 except that a vinyl chloride-vinyl acetate copolymer was used as the intermediate film.

  As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 42.6% and 0.2%, respectively, and the pummel value was 5 and good.

A laminated structure C according to Example 3 in the same manner as in Example 1 except that 14.1 m ² / g LaB ₆ fine particles were used instead of LaB ₆ fine particles having a specific surface area of 19.7 m ² / g in Example 1. Was made.

  As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 42.9% and 0.3%, respectively, and the Pummel value was 5 and good.

A laminated structure according to Example 4 in the same manner as in Example 1 except that CeB ₆ having a specific surface area of 16.5 m ² / g was used instead of LaB ₆ fine particles having a specific surface area of 19.7 m ² / g in Example 1. D was produced.

  As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 43.9% and 0.3%, respectively, and the Pummel value was 5 and good.

A laminated structure according to Example 5 in the same manner as in Example 1 except that NdB ₆ having a specific surface area of 17.3 m ² / g was used instead of LaB ₆ fine particles having a specific surface area of 19.7 m ² / g in Example 1. E was produced.

  As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 43.9% and 0.2%, respectively, and the Pummel value was 5 and good.

The combined structure according to Example 6 in the same manner except for using the PrB ₆ having a specific surface area of 15.1m ² / g instead of the LaB ₆ fine particles having a specific surface area of 19.7 m ² / g in Example 1 and Example 1 F was produced.

As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 44.1% and 0.3%, respectively, and the Pummel value was 5 and good.
[ Reference Example 7 ]

After mixing 30% by weight of tin-containing indium oxide (ITO) fine particles having a specific surface area of 77.6 m ² / g, 56% by weight of isobutyl alcohol, and 14% by weight of a dispersant, and filling the container with glass beads having a diameter of 0.15 mm, An ITO dispersion liquid was prepared by performing a bead mill dispersion treatment for 1 hour (liquid B).

Next, the A liquid and the prepared B liquid were mixed well, UV curable resin (trade name grade UV3701 manufactured by Toa Gosei Co., Ltd.) and ethanol as a diluent were added, the LaB ₆ concentration was 0.2 wt%, ITO A coating solution for forming a solar radiation shielding layer having a concentration of 9.8% by weight was prepared.

And the laminated structure G which concerns on the reference example 7 was produced like Example 1 except having applied this coating liquid for solar radiation shielding layer formation.

As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 37.7% and 0.2%, respectively, and the pummel value was 5 and good.
[ Reference Example 8 ]

The combined structure H, except for using the ITO fine particles having a specific surface area of 58.1m ² / g instead of the ITO fine particles having a specific surface area of 77.6m ² / g in Example 7 according to the reference example 8 in the same manner as in Reference Example 7 Was made.

As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 38.5% and 0.2%, respectively, and the pummel value was 5 and good.
[ Reference Example 9 ]

The combined structure I, except for using the ITO fine particles having a specific surface area of 97.1m ² / g instead of the ITO fine particles having a specific surface area of 77.6m ² / g in Example 7 according to the reference example 9 in the same manner as in Reference Example 7 Was made.

As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 37.2% and 0.2%, respectively, and the Pummel value was 5 and good.
[ Reference Example 10 ]

A laminated structure J according to Reference Example 10 was prepared in the same manner as in Reference Example 7 except that a coating solution for forming a solar radiation shielding layer having a LaB ₆ concentration of 0.05% by weight and an ITO concentration of 9.95% by weight was prepared in Reference Example 7. Produced.

As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 37.1% and 0.3%, respectively, and the pummel value was 5 and good.
[ Reference Example 11 ]

After mixing 30% by weight of antimony-containing tin oxide (ATO) fine particles having a specific surface area of 43.7 m ² / g, 55% by weight of isobutyl alcohol, and 15% by weight of a dispersant, the mixture is filled into a container with glass beads having a diameter of 0.15 mm. A 5-hour bead mill dispersion treatment was carried out to prepare an ATO dispersion (solution C).

The above liquid A and the prepared liquid C are mixed well, UV curable resin (trade name grade UV3701 manufactured by Toa Gosei Co., Ltd.) and ethanol are added as a diluent, LaB ₆ fine particle concentration is 0.2% by weight, ATO fine particle concentration A coating solution for forming a solar radiation shielding layer having a weight of 9.8% by weight was prepared.

And the laminated structure K which concerns on the reference example 11 was produced like Example 1 except having applied this coating liquid for solar radiation shielding layer formation.

  As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 42.8% and 0.4%, respectively, and the Pummel value was 5 and good.

  In Example 1, ethylene-vinyl acetate was used as an adhesive layer between a solar radiation shielding layer formed on one side of a ductile polyester film and a green glass laminated surface having a thickness of 100 mm × 100 mm × about 2 mm in contact with the solar radiation shielding layer. A laminated structure L according to Example 12 was produced in the same manner as in Example 1 except that the copolymer was interposed.

  As shown in Table 1, the solar radiation transmittance and haze value when the visible light transmittance was 72% were 42.1% and 0.2%, respectively, and the Pummel value was 5 and good.

The solar shading layer-forming coating solution applied in Example 1 was applied to one side of an intermediate film polyvinyl butyral (thickness 0.76 mm) formed into a sheet and dried at 105 ° C. to form a solar shading layer. .

Then, the polyvinyl butyral for interlayer film having a solar radiation shielding layer formed on one side is interposed between two green glasses having dimensions of 100 mm × 100 mm × about 2 mm, and is temporarily mounted by heating to 80 ° C. Then, this mounting | wearing by an autoclave was performed on the conditions of 14 kg / cm < ² > at 140 degreeC, and the laminated structure M based on Example 13 was produced.

  As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 44.3% and 0.3%, respectively, and the pummel value was 5 and good.

A laminated structure N according to Example 14 was produced in the same manner as in Example 13 except that LaB ₆ fine particles applied in Example 3 were used.

  As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 43.1% and 0.3%, respectively, and the Pummel value was 5 and good.

A laminated structure O according to Example 15 was produced in the same manner as in Example 13 except that CeB ₆ applied in Example 4 was used.

  As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 45.9% and 0.3%, respectively, and the Pummel value was 5 and good.

A laminated structure P according to Example 16 was produced in the same manner as in Example 13 except that NdB ₆ applied in Example 5 was used.

  As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 46.0% and 0.3%, respectively, and the Pummel value was 5 and good.

A laminated structure Q according to Example 17 was produced in the same manner as in Example 13 except that PrB ₆ applied in Example 6 was used.

As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 46.1% and 0.2%, respectively, and the pummel value was 5 and good.
[ Reference Example 18 ]

A laminated structure R according to Reference Example 18 was produced in the same manner as in Example 13 except that the coating solution for forming the solar radiation shielding layer applied in Reference Example 7 was used.

As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 39.1% and 0.3%, respectively, and the Pummel value was 5 and good.
[ Reference Example 19 ]

A laminated structure S according to Reference Example 19 was produced in the same manner as in Example 13 except that the solar shading layer forming coating solution applied in Reference Example 9 was used.

As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 38.7% and 0.3%, respectively, and the Pummel value was 5 and good.
[ Reference Example 20 ]

A laminated structure T according to Reference Example 20 was produced in the same manner as in Example 13 except that the solar shading layer forming coating solution applied in Reference Example 10 was used.

As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 39.3% and 0.3%, respectively, and the Pummel value was 5 and good.
[ Reference Example 21 ]

A laminated structure U according to Reference Example 21 was produced in the same manner as in Example 13 except that the solar shading layer forming coating solution applied in Reference Example 11 was used.

As shown in Table 2, the solar radiation transmittance and haze value when the visible light transmittance was 75% were 44.0% and 0.2%, respectively, and the Pummel value was 5 and good.
[Comparative Example 1]
The liquid A prepared in Example 1 and the liquid B prepared in Reference Example 7 were added to polyvinyl butyral, triethylene glycol-di-2-ethylbutyrate was added as a plasticizer, and the LaB ₆ concentration was 0.0015% by weight. An intermediate film composition was prepared such that the ITO concentration was 0.15 wt% and the polyvinyl butyral resin was 70 wt%.

  Next, the prepared intermediate film composition was kneaded with a roll and formed into a 0.76 mm thick sheet to produce an intermediate film.

Then, the intermediate film is interposed between a pair of green glasses having dimensions of 100 mm × 100 mm × about 2 mm thick, temporarily mounted by heating to 80 ° C., and then fully mounted by autoclave at 140 ° C. under the condition of 14 kg / cm ^2. The laminated structure V according to Comparative Example 1 was manufactured.

  As shown in Table 2, the solar radiation transmittance was 46.0% when the visible light transmittance was 75%, and the pummel value was 5 and good, but the haze values were 0.7% and 0.4%. It was over.

  Therefore, it did not have a good solar shading function under the conditions of a haze value of 0.4% or less and high visible light transmittance.

「評 価」
（１）実施例１〜実施例６においては、ＬａＢ₆等の濃度が０．２重量％の日射遮蔽層形成用塗布液を調製して日射遮蔽用合わせ構造体Ａ〜Ｆが製造されている。

"Evaluation"
(1) In Examples 1 to 6, solar-shielding laminated structures A to F are manufactured by preparing a solar-shielding layer-forming coating solution having a concentration of 0.2% by weight such as LaB ₆ . .

Then, the lower partial concentration of LaB _6, etc. is solar shading component, the manufacturing cost of the conventional method and the comparison with solar shielding laminated structure A~F has become inexpensive, haze value of 0.4% or less and It is confirmed that a solar radiation shielding laminated structure having a solar radiation transmittance of about 42 to 46% (42.3 to 44.1%) under a condition where the visible light transmittance is 72% is obtained.

In addition, in the solar shading laminated structures L to Q according to Examples 12 to 17 to which the solar shading layer forming coating liquid prepared in Examples 1 to 6 is applied, the solar shading component LaB ₆ or the like is used. Since the concentration is low, the manufacturing cost of the solar radiation shielding laminated structures L to Q is lower than that of the conventional method, but the haze value is 0.4% or less and the visible light transmittance is 72% to 75%. It is confirmed that a solar radiation shielding laminated structure having a solar transmittance of about 42 to 46% (42.1 to 46.1%) under the conditions is obtained.

Further, regarding the solar shading laminated structures K and U according to Reference Examples 11 and 21, to which the solar shading layer forming coating liquid having a LaB ₆ fine particle concentration of 0.2 wt% and an ATO fine particle concentration of 9.8 wt% was applied. Is low in the concentration of LaB ₆ and the ATO fine particle is an inexpensive solar shielding component, so the manufacturing cost of the solar shielding laminated structure is lower than that of the conventional method, but the haze value is 0.4% or less. In addition, it is confirmed that a solar radiation shielding laminated structure having a solar radiation transmittance of about 42 to 46% (42.8 to 44.0%) under a condition where the visible light transmittance is 72% is obtained.
(2) On the other hand, in Reference Examples 7 to 9 , a solar radiation shielding layer forming coating solution having a LaB ₆ concentration of 0.2% by weight and an ITO concentration of 9.8% by weight was prepared to provide a solar radiation shielding laminated structure. In addition, in Reference Example 10 , a solar radiation shielding layer-forming coating solution having a LaB ₆ concentration of 0.05% by weight and an ITO concentration of 9.95% by weight was prepared to provide a solar radiation shielding laminated structure. J is manufactured.

  And since the ITO fine particles are applied at a high concentration, the manufacturing cost of the solar radiation shielding laminated structures G to J is high, but the haze value is 0.4% or less (0.2 to 0.3%). And it is confirmed that the solar radiation shielding laminated structure in which the solar radiation transmittance under the condition where the visible light transmittance is 72% is set to less than 40% (37.1 to 38.5%) can be provided.

In addition, also in the solar shading laminated structures R to T according to Reference Examples 18 to 20 to which the solar shading layer forming coating liquid adjusted in Reference Examples 7 to 10 is applied, the haze value is 0.4%. It is confirmed that the solar radiation transmittance is set to less than 40% (38.7 to 39.3%) under the following conditions (0.3%) and the visible light transmittance is 75%.

The composition sectional view of the laminated structure for solar radiation shielding concerning the present invention. Sectional drawing of a structure of the laminated structure for solar radiation shielding which concerns on the modification of this invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Plate-shaped body 2 Solar radiation shielding layer 3 Ductile film board | substrate 4 Intermediate film 5 Plate-shaped body 10 Solar radiation shielding film

Claims (2)

In a solar radiation shielding laminated structure in which an intervening layer having a solar radiation shielding function is interposed between at least two transparent glass or plastic plates,
The intervening layer is constituted by the solar radiation shielding layer of the solar radiation shielding film in which the ultraviolet radiation curable resin made of acrylic resin and the solar radiation shielding layer containing hexaboride fine particles are formed on one side of the ductile film substrate, and the one plate The solar radiation shielding layer of the solar radiation shielding film is placed in contact with the mating surface side of the sheet-like body, and a vinyl-based resin is placed between the mating surface side of the other plate-like body and the ductile film substrate side of the solar radiation shielding film. Solar radiation shielding, characterized in that an intermediate film as a main component is disposed, and has an optical characteristic of a solar light transmittance of 42 to 46% and a haze value of 0.4% or less at a visible light transmittance of 72%. Laminated structure. In a solar radiation shielding laminated structure in which an intervening layer having a solar radiation shielding function is interposed between at least two transparent glass or plastic plates,
An intervening layer is constituted by the above-mentioned solar shading layer of an intermediate film mainly composed of a vinyl resin in which a UV-curing resin made of acrylic resin and a solar shading layer containing hexaboride fine particles are formed on one side. The solar radiation shielding layer of the intermediate film is in contact with the mating surface side of one plate, and the opposite side of the intermediate film is in contact with the mating surface of the other plate, and the visible light transmittance is Having a solar transmittance of 42 to 46% and a haze value of 0.4% or less at 75% of the solar radiation shielding laminated structure.

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