JP5496807B2 - Intermediate film for laminated glass, method for producing the same, and laminated glass using the same - Google Patents

Description

  The present invention relates to an interlayer film for laminated glass having excellent transparency, adhesiveness, durability, and heat ray shielding properties. Moreover, it is related with the manufacturing method and the laminated glass using the same.

  Laminated glass is widely used for vehicles such as automobiles, window glass for buildings, etc., for improving safety such as prevention of glass scattering. Examples of such a laminated glass include those laminated with an interlayer film for laminated glass made of plasticized polyvinyl butyral resin or the like interposed between at least one pair of glass plates. However, when an ordinary interlayer film for laminated glass is used, there is a problem in that near infrared rays (heat rays) having a large thermal effect cannot be shielded, and the provision of heat shielding properties has been demanded.

  For the purpose of imparting heat ray shielding properties, by adding fine particles having heat ray absorbing performance such as tin-doped indium oxide (ITO) fine particles and antimony-doped tin oxide (ATO) fine particles to the polymer, the heat-shielding function is provided. An interlayer film for glass has been proposed. Such a laminated glass can not only provide a heat ray cutting function to an ordinary laminated glass, but also has excellent electromagnetic wave permeability as compared with a so-called heat ray reflective laminated glass.

  Laminated glass using the interlayer film for laminated glass containing fine particles having such heat ray absorbing performance has better weather resistance and stable for a long period of time compared to the case of containing an organic compound having the same heat ray shielding performance. The heat ray cutting function can be demonstrated. However, when exposed to high energy rays such as UV light for a long period of time, the deterioration of the resin due to the photocatalytic activity of the heat ray shielding fine particles and the alteration of the heat ray shielding fine particles themselves cause deterioration of the visible light transmittance and yellowing of the laminated glass. In particular, when used for a vehicle, it may cause a serious problem in safety.

  As a technique for suppressing deterioration due to such heat ray shielding fine particles, a technique of surface treatment with a metal alkoxide, a coupling agent, or the like is known (see Patent Documents 1 to 3). By using such surface-treated heat ray shielding fine particles, deterioration of the matrix resin and alteration of the heat ray shielding fine particles can be suppressed. However, since such a surface treatment also affects the dispersibility of the particles, it is necessary to construct a dispersion method suitable for the surface-treated particles when trying to obtain a highly transparent laminated glass. was there. In particular, the metal ions contained in the adhesion control agent that is usually added for the purpose of controlling the adhesion force have a strong interaction with the particle surface and greatly affect the dispersibility. When heat ray shielding fine particles are used in combination with a resin, it is difficult to reduce haze.

  In Patent Documents 4 and 5, laminated glass with high transparency is obtained in laminated glass using ITO or ATO-containing interlayer film to which magnesium acetate is added as an adhesion control agent. In these cases, an inert substance is used. No ITO or ATO fine particles surface-treated with. Since the surface-treated particles are greatly different in dispersibility from ordinary particles, it has not been possible to obtain high transparency simply by controlling the addition amount of the adhesion control agent. Patent Document 6 describes a method for controlling the adhesive force of laminated glass comprising an interlayer film for laminated glass containing ITO fine particles surface-treated with an inert substance. In this case, an adhesive force controlling agent is added. There are no examples. Actually, it is very difficult to stably control the adhesion between glass and interlayer film without adding an adhesion control agent. In addition to controlling the glass adhesion, both weather resistance and high transparency are compatible. The technique to make it desired was desired.

JP 2000-016841 A JP 2001-240769 A WO2005 / 118503 JP 2001-302288 A Japanese Patent No. 3897519 JP 2006-27962 A

  The present invention has been made to solve the above-described problems, and aims to provide an interlayer film for laminated glass that is excellent in transparency and heat ray shielding properties while maintaining adhesiveness and durability. is there.

  As a result of intensive studies on the above problems, the heat-shielding fine particles (C) surface-treated with the polyvinyl acetal (A), the plasticizer (B), and the organosilicon compound having a hydrolyzable substituent (hereinafter simply referred to as “heat rays”). An interlayer film for laminated glass comprising at least one resin composition layer containing an alkali metal salt and / or an alkaline earth metal salt (E). The resin composition layer is melt-molded after separately mixing the heat ray shielding fine particles (C) and the alkali metal salt and / or alkaline earth metal salt (E) with respect to the polyvinyl acetal (A). The interlayer film for laminated glass characterized in that it is obtained by suppressing aggregation of the heat-shielding fine particles (C), exhibiting high transparency, and improving durability and glass adhesion We have found that it is.

  Here, the resin composition layer is a dispersion of the heat ray shielding fine particles (C) and the dispersion of alkali metal salt and / or alkaline earth metal salt (E) with respect to the polyvinyl acetal (A). (D2) is preferably mixed and then melt-molded, and the dispersion (d1) is more preferably subjected to wet pulverization.

  Further, from the viewpoint of adhesive force control and heat resistance improvement, the resin composition layer contains 0 alkali metal salt and / or alkaline earth metal salt (E) in terms of metal with respect to 100 parts by weight of polyvinyl acetal (A). It is preferable to contain 0.0001-0.04 weight part. Furthermore, from the viewpoint of heat ray shielding performance, the resin composition layer is heat ray shielding fine particles (C) 0.001 to 2 parts by weight with respect to 100 parts by weight of the total amount of the polyvinyl acetal (A) and the plasticizer (B). It is preferable to contain.

  The heat ray shielding fine particles (C) are tin-doped indium oxide, antimony-doped tin oxide, aluminum-doped zinc oxide, indium-doped zinc oxide, gallium-doped zinc oxide, tungsten oxide, lanthanum hexaboride, cerium hexaboride, anhydrous antimonic acid It is preferably at least one selected from the group consisting of zinc and copper sulfide, more preferably anhydrous zinc antimonate.

  In addition, from the viewpoint of durability such as light resistance and glass adhesiveness, the resin composition layer, the second containing the polyvinyl acetal (A ′), the plasticizer (B ′), and the ultraviolet absorber (D). The interlayer film for laminated glass including the resin composition layer is also preferable. In this case, it is more preferable that the resin composition layer has a structure sandwiched between two second resin composition layers.

  Further, in the laminated glass produced by sandwiching and bonding the interlayer film for laminated glass between two 2 mm thick clear glasses, the 1st mode damping performance at 20 ° C. when measured according to ISO 16940 is 22% or more. It is preferable that the damping performance of the 1st mode at 10 ° C. is preferably 10% or more.

  Furthermore, the vinyl alcohol unit amount in the polyvinyl acetal (A) is 22 mol% or less, the vinyl acetate unit amount is 5 to 8 mol%, and the vinyl alcohol unit amount in the polyvinyl acetal (A ′) is 25 to 34 mol. %, And the vinyl acetate unit amount is preferably 0.1 to 11 mol%.

  Moreover, it is also preferable that the difference of content of the plasticizer contained in the said resin composition layer and content of the plasticizer contained in the said 2nd resin composition layer is 5 weight% or more.

  In the laminated glass produced by sandwiching and bonding the interlayer film for laminated glass between two 2 mm thick clear glasses, it is also preferred that the haze measured according to JIS K7105 is 2% or less.

  Moreover, the said subject is also solved by providing the laminated glass formed by adhere | attaching a several glass plate using the said intermediate film for laminated glasses.

  The present invention relates to the above interlayer film for laminated glass, comprising a step of melt-mixing the dispersion (d1) of the heat ray shielding fine particles (C) and the plasticizer (B) with the polyvinyl acetal (A) and forming the film into a film. A manufacturing method is also included. In this case, the dispersion (d1) of the heat ray shielding fine particles (C) and the alkali metal salt and / or alkaline earth metal salt (E) are separately mixed with the polyvinyl acetal (A), and then formed into a film. Preferably, the method includes a step of melt-molding, and more preferably includes a step of preparing surface-treated heat ray shielding fine particles (C) by baking a mixture of an organosilicon compound and heat ray shielding fine particles at 100 to 400 ° C. It is further preferable to include a step of preparing a dispersion (d1) of the heat ray shielding fine particles (C) by subjecting the heat ray shielding fine particles (C) to pulverization.

  The interlayer film for laminated glass of the present invention is excellent in transparency, adhesiveness, durability and heat ray shielding properties. Therefore, by using the intermediate film, a laminated glass excellent in transparency, adhesiveness, durability and heat ray shielding can be provided.

  The interlayer film for laminated glass of the present invention comprises a polyvinyl acetal (A), a plasticizer (B), heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent, and an alkali metal salt and At least one resin composition layer containing an alkaline earth metal salt (E) is included.

  The polyvinyl acetal (A) contained in the resin composition layer is a reaction between polyvinyl alcohol (hereinafter sometimes abbreviated as PVA) and an aldehyde in water and / or an organic solvent in the presence of an acid catalyst. In some cases, the product obtained by neutralization can be obtained by neutralization, washing, and drying. The structure of the resulting polyvinyl acetal (A) is shown in the following general formula (I).

上記一般式（Ｉ）において、ｎ、Ｒ_ａ、ｋ_（ａ）、ｌおよびｍの意味は以下に示すとおりである。

ｎ： アセタール化に用いたアルデヒドの種類（整数）
Ｒ_ａ： ａ番目（ａは１からｎまでの整数）のアルデヒド残基
ｋ_（ａ） ：アルデヒド残基Ｒ_ａを含むアセタール単位の割合（モル比）
ｌ： ビニルアルコール単位の割合（モル比）
ｍ： ビニルアセテート単位の割合（モル比）
ただし、ｋ_（１）＋ｋ_（２）＋・・・＋ｋ_（ｎ）＋ｌ＋ｍ＝１

上記一般式（Ｉ）において、各単位の配列の仕方は特に制限されず、ブロック的であっても、ランダム的であってもよい。

In the general formula (I), the meanings of n, R _a , k _(a) , l and m are as follows.

n: Type of aldehyde used for acetalization (integer)
R _a : a-th aldehyde residue (a is an integer from 1 to n) k _(a) : ratio (molar ratio) of acetal units containing aldehyde residue R _a
l: Ratio of vinyl alcohol units (molar ratio)
m: Ratio of vinyl acetate units (molar ratio)
However, k ₍₁₎ + k ₍₂₎ +... + K _(n) + l + m = 1

In the general formula (I), the arrangement of the units is not particularly limited, and may be block or random.

  The operations of acetalization reaction, neutralization, washing, and dehydration when producing the polyvinyl acetal (A) are not particularly limited, and can be performed by known methods. For example, an aqueous solvent method in which an aqueous solution of PVA and an aldehyde are acetalized in the presence of an acid catalyst to precipitate resin particles, PVA is dispersed in an organic solvent, and an aldehyde is acetalized in the presence of an acid catalyst. An organic solvent method in which this reaction solution is precipitated by adding it to water or the like, which is a poor solvent for polyvinyl acetal (A), can be employed. Whichever method is used, a slurry in which the polyvinyl acetal (A) is dispersed in the medium is obtained.

  Since the slurry obtained by the above method is acidic by an acid catalyst, an alkali neutralizer such as sodium hydroxide or sodium carbonate is added as necessary, and the pH is 4.5 or more, preferably Adjust to 6-9, more preferably 6-8.

  As the PVA used for the production of the polyvinyl acetal (A), those having a viscosity average polymerization degree of 500 to 4000, preferably 1000 to 2500 are generally used. The viscosity average polymerization degree of the polyvinyl acetal (A) is substantially the same as the viscosity average polymerization degree of the raw material PVA. When the viscosity average polymerization degree of the raw material PVA is less than 500, the mechanical properties are insufficient, and the mechanical properties, particularly toughness, of the interlayer film for laminated glass of the present invention may be insufficient. On the other hand, when the viscosity average polymerization degree of the raw material PVA exceeds 4000, the melt viscosity at the time of melt molding becomes too high, and a problem may occur in the production process. In addition, when using 2 or more types of polyvinyl acetal as polyvinyl acetal (A), the average value which considered the compounding quantity should just satisfy the said range. Here, the polymerization degree of PVA can be measured according to JIS K 6726. Specifically, after re-saponifying and purifying PVA, it can be determined from the intrinsic viscosity measured in water at 30 ° C.

  It does not specifically limit as said PVA, Conventionally well-known PVA, such as what was manufactured by saponifying polyvinyl acetate etc. in presence of an alkali, an acid, ammonia water, etc., can be used. Although fully saponified PVA or partially saponified PVA may be used, the degree of saponification of PVA is preferably 80 mol% or more. In addition, a partially crosslinked structure may be included. The PVA may be a single PVA or a mixture of two or more. When two or more types of PVA are used, the average value considering the blending amount may satisfy the saponification degree range.

  As the PVA, a saponified product of a copolymer with a monomer copolymerizable with vinyl acetate or the like, such as an ethylene-vinyl alcohol copolymer or a partially saponified ethylene-vinyl alcohol copolymer, can also be used. Furthermore, modified PVA modified with carboxylic acid or the like can also be used.

  The aldehyde used for acetalizing PVA is not particularly limited. For example, formaldehyde (including paraformaldehyde), acetaldehyde (including paraacetaldehyde), propionaldehyde, butyraldehyde, amylaldehyde, hexylaldehyde, heptylaldehyde, 2-ethylhexylaldehyde, cyclohexylaldehyde, furfural, glyoxal, glutaraldehyde, benzaldehyde, 2-methylbenzaldehyde, 3-methylbenzaldehyde, 4-methylbenzaldehyde, p-hydroxybenzaldehyde, m-hydroxybenzaldehyde, phenylacetaldehyde, β-phenylpropionaldehyde Etc. These aldehydes may be used alone or in combination of two or more. Among these aldehydes, butyraldehyde is preferably used from the viewpoint of ease of production.

The polyvinyl acetal (A) obtained by acetalizing PVA using butyraldehyde is particularly referred to as polyvinyl butyral. In the present invention, among the acetal units present in the polyvinyl acetal (A), polyvinyl butyral having a butyral unit ratio (see the following formula) exceeding 0.9 is preferable. That is, in the structural formula of the polyvinyl acetal (A) represented by the above formula (I), when R ₁ = C ₃ H ₇ (residue of butyraldehyde), k ₍₁₎ / (k ₍₁₎ + k _{( 2)} + ... + k _(n) )> 0.9 is preferred.

  The acid catalyst for the acetalization reaction is not particularly limited, and examples thereof include organic acids such as acetic acid and p-toluenesulfonic acid, and inorganic acids such as nitric acid, sulfuric acid, and hydrochloric acid. Further, the neutralizing agent for the acetalization reaction is not particularly limited. For example, alkali such as sodium hydroxide, potassium hydroxide, ammonia, sodium acetate, sodium carbonate, sodium bicarbonate, potassium carbonate; ethylene oxide, etc. Alkylene oxides; glycidyl ethers such as ethylene glycol diglycidyl ether.

The degree of acetalization, the amount of vinyl alcohol units and the amount of vinyl acetate units (mol%) of the polyvinyl acetal (A) can be defined by the following formula.

Acetalization degree (mol%) = [(k ₍₁₎ + k ₍₂₎ +... + K _(n) ) × 2]
/ [(K ₍₁₎ + k ₍₂₎ +... + K _(n) ) × 2 + l + m] × 100
Vinyl alcohol unit amount (mol%)
= [L / [(k ₍₁₎ + k ₍₂₎ +... + K _(n) ) × 2 + l + m] × 100
Vinyl acetate unit amount (mol%)
= [M / [(k ₍₁₎ + k ₍₂₎ +... + K _(n) ) × 2 + l + m] × 100

  The degree of acetalization of the polyvinyl acetal (A) is preferably 55 to 83 mol%. Polyvinyl acetal (A) having a degree of acetalization of less than 55 mol% is disadvantageous in terms of cost performance because of high production costs, difficulty in obtaining, and poor melt processability. Polyvinyl acetal (A) exceeding 83 mol% may be disadvantageous in terms of productivity because it requires a longer acetalization reaction time. A polyvinyl acetal (A) may be used individually by 1 type, and may be used in combination of 2 or more type. When using 2 or more types of polyvinyl acetals, the average value which considered the compounding quantity should just satisfy the range of the said acetalization degree.

  The resin composition layer constituting the interlayer film for laminated glass of the present invention contains a plasticizer (B). As the plasticizer (B), known plasticizers used for plasticizing the polyvinyl acetal (A) can be used. Preferably, one or two or more kinds of organic plasticizers such as aliphatic polyol monobasic acid esters and linear or branched alcohol polybasic acid esters are used.

  The monobasic acid ester of the aliphatic polyol is not particularly limited, but a monobasic acid ester of an aliphatic diol is preferable, and a monobasic acid ester of polyalkylene glycol, particularly polyethylene glycol is more preferable. Specifically, an ester composed of di, tri, or tetraalkylene glycol and a monobasic acid having 4 to 10 carbon atoms is preferably used.

  Polybasic acid ester of linear or branched alcohol is not particularly limited, for example, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, phthalic acid, cyclohexanedicarboxylic acid, phosphoric acid, An ester composed of a linear or branched alcohol having 4 to 10 carbon atoms is preferably used.

  Among the plasticizer groups, for example, triethylene glycol-di-2-ethylbutyrate, triethylene glycol-di-2-ethylhexanoate, triethylene glycol-di-n-heptanoate, tetraethylene glycol-di-2 -Ethylhexanoate, tetraethylene glycol-di-n-heptanoate, oligoethylene glycol-di-2-ethylhexanoate, triethylene glycol-di-isononanoate, triethylene glycol-di-2-propylhexanoate, Di-propylene glycol benzoate, dihexyl adipate, di-2-butoxyethyl adipate, di-2-butoxyethoxyethyl adipate, di-2-ethylhexyl adipate, dibutyl sebacate, di-2-butoxyethyl sebacate, 2-ethylhexyl sebacate, di-2-ethylhexyl phthalate, di - isononyl phthalate, tris 2-ethylhexyl phosphate, or one or two of such diisononyl cyclohexanedicarboxylate is preferably used.

  It is preferable that the addition amount of a plasticizer (B) is 20-100 weight part with respect to 100 weight part of polyvinyl acetal (A). If it is less than 20 parts by weight, the impact resistance of the resulting interlayer film or laminated glass may be insufficient. Conversely, if it exceeds 100 parts by weight, the plasticizer (B) bleeds out and the interlayer film obtained is obtained. In addition, the transparency of the laminated glass may be reduced, or the adhesion between the glass and the interlayer film may be impaired.

  The resin composition layer constituting the interlayer film for laminated glass of the present invention contains heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent for the purpose of imparting heat shielding properties. The heat ray shielding fine particles used in this case are not particularly limited as long as they have a property of absorbing at least light in the near-infrared wavelength region as a function. For example, tin-doped indium oxide, antimony-doped tin oxide, aluminum-doped oxidation Examples thereof include zinc, indium-doped zinc oxide, gallium-doped zinc oxide, tungsten oxide, lanthanum hexaboride, cerium hexaboride, anhydrous zinc antimonate, and copper sulfide. These may be used alone or in combination of two or more. Among these, it is preferable to contain anhydrous zinc antimonate from the viewpoints of performance, safety, raw material availability, price, and the like.

  The heat ray shielding fine particles are surface-treated with an organosilicon compound having a hydrolyzable substituent. By treating the particle surface with the organosilicon compound, it is possible to suppress deterioration of the resin and alteration of the heat ray shielding fine particles. In general, methods for surface treatment of inorganic fine particles with metal oxides are known, but the difficulty of the treatment depends on the surface state of the target inorganic fine particles, specifically the amount of hydroxyl groups present on the particle surface. Depending on the type of inorganic fine particles, the surface treatment may be very difficult. In particular, the anhydrous zinc antimonate is difficult to surface-treat because its surface state is different from other heat ray shielding fine particles, and there are almost no examples of treatment with an organosilicon compound. It can also be applied to zinc acid.

The organosilicon compound having the hydrolyzable substituent is not particularly limited as long as it has at least one hydrolyzable substituent that can be cleaved by hydrolysis. For example, an organosilicon compound represented by the following formula (II) is used.

Si (OR ¹ ) _a R ² _b (II)

In formula (II), R ¹ represents a hydrogen atom or an alkyl group, R ² represents a hydrogen atom, a halogen atom, an amino group, an amide group, an acyl group, an allyl group, an aryl group, a vinyl group, an epoxy group, a sulfyl group, The substituent includes a hydroxyl group, a mercapto group, a linear or cyclic alkyl group that may be partially substituted, and the like. A and b represent an integer of 0 to 4, and a + b is 4.

  Among the organosilicon compounds represented by the above general formula (II), for example, methyltrimethoxysilane, dimethyldimethoxysilane, tetraethoxysilane, methyltriethoxysilane, dimethyldiethoxysilane, ethyltriethoxysilane, cyclohexylmethyldimethoxysilane, Methyloctyldimethoxysilane, methylphenyldimethoxysilane, diphenyldiethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, isobutyltrimethoxysilane, isobutyltriethoxysilane, hexyl Trimethoxysilane, hexyltriethoxysilane, octyltrimethoxysilane, octyltriethoxysilane, decyltrimethoxysilane, octade Rutrimethoxysilane, trifluoropropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, tris (2-methoxyethoxy) vinylsilane, allyltriethoxysilane, acetoxymethyltrimethoxysilane, acetoxymethyltriethoxysilane, acetoxyethyltri Methoxysilane, acetoxyethyltriethoxysilane, acetoxypropyltrimethoxysilane, 2-acetoxypolyethyleneoxypropyltriethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropyltriethoxysilane, p-styryltrimethoxysilane, 3-meta Acryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltriethoxysilane, acryloxymethyltrimethoxysilane, 2-acryloxyethoxytrimethoxysilane 3-acryloxypropyltrimethoxysilane, hydroxy (polyethyleneoxy) propyltriethoxysilane, 2-hydroxy-4- (3-methyldiethoxysilylpropoxy) diphenyl ketone, 2-hydroxy-4- (3-triethoxysilyl) Propoxy) diphenyl ketone, N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane, N-2- (aminoethyl) -3-aminopropyltrimethoxysilane, N-2- (a) Noethyl) -3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-triethoxysilyl-N- (1,3-dimethyl-butylidene) propylamine, N-phenyl -3-aminopropyltrimethoxysilane, N- (vinylbenzyl) -2-aminoethyl-3-aminopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, chlorotrimethoxysilane, chlorotriethoxysilane, chloromethyltri Ethoxysilane, 3-chloropropyltrimethoxysilane, p-chloromethylphenyltrimethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3-mercaptopropyltrimethoxysilane, bis (triethoxysilylpropyl) te Rasulfide, 3-isocyanatopropyltriethoxysilane, methyltrichlorosilane, dimethyldichlorosilane, trimethylchlorosilane, phenyltrichlorosilane, vinyltrichlorosilane, hexamethyldisilazane, 1,3,5,7-tetraethoxy-1,3,5 , 7-tetramethylcyclotetrasiloxane, hexaphenylcyclotrisiloxane and the like. These may be used alone or in combination of two or more.

  In the resin composition layer constituting the interlayer film for laminated glass of the present invention, the heat ray shielding fine particles (C) are 0.001 parts per 100 parts by weight of the total amount of the polyvinyl acetal (A) and the plasticizer (B). It is preferable to contain -2 weight part. If the content is 0.001 part by weight or less, the expected heat ray shielding effect may not be obtained. More preferably, it is 0.002 weight part or more, More preferably, it is 0.005 weight part or more. Moreover, when content exceeds 2 weight part, there exists a possibility that the transparency of a laminated glass may be impaired. More preferably, it is 1.5 weight part or less, More preferably, it is 1 weight part or less.

  In the heat ray shielding fine particles (C), the fixed amount of the organosilicon compound having a hydrolyzable substituent is preferably 0.05 to 50 parts by weight with respect to 100 parts by weight of the heat ray shielding fine particles (C). If the fixing amount of the organosilicon compound is less than 0.05 parts by weight, the fixing amount of the organosilicon compound on the surface of the particle is not sufficient, and it may be difficult to obtain effects such as a reduction in photocatalytic activity and prevention of particle alteration. is there. More preferably, it is 0.1 parts by weight or more. On the other hand, if it exceeds 50 parts by weight, the particles may be coarsened and the intended dispersion may not be obtained, and the surface treatment may be expensive. More preferably, it is 40 parts by weight or less.

  As a method for producing heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent, a dispersion in which the heat ray shielding fine particles are finely dispersed is prepared in advance, and an organosilicon compound is added thereto. The method is preferred. By this method, the organosilicon compound can be unevenly distributed on the surface of the nano-sized particles, and as a result, the entire particles can be treated uniformly. Moreover, after adding an organosilicon compound, it is preferable to once distill off a dispersion medium and to fire the powder of the obtained mixture at 100-400 degreeC. By once removing the solvent and then treating at a high temperature, the organosilicon compound can be fixed on the surface of the heat ray shielding fine particles by a strong chemical bond. Thereby, detachment | desorption of the organosilicon compound at the time of melt-kneading can be suppressed, and a higher surface treatment effect can be obtained.

  The solvent contained in the dispersion of the heat ray shielding fine particles is not particularly limited, but water or an organic solvent having high affinity with water is preferably used in consideration of the hydrolyzability of the organosilicon compound. Examples of such organic solvents include methanol, ethanol, n-propanol, i-propanol, n-butanol, ethylene glycol, diethylene glycol, hexylene glycol, tetrahydrofuran, acetone, γ-butyrolactone, ε-caprolactone, and N-methylpyrrolidone. N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, and the like can be used.

  The resin composition layer constituting the interlayer film for laminated glass of the present invention contains an alkali metal salt and / or an alkaline earth metal salt (E) for the purpose of adhesive force control or resin pH adjustment. Although it does not specifically limit as alkali metal salt / alkaline earth metal salt, Sodium, potassium, magnesium etc. are mentioned as an alkali metal / alkaline earth metal which forms a salt. Examples of the acid that forms a salt include linear carboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, hexanoic acid and octanoic acid, and branched carboxylic acids such as 2-ethylbutanoic acid and 2-ethylhexanoic acid. Examples thereof include organic acids such as acids, and inorganic acids such as hydrochloric acid, nitric acid, and sulfuric acid. These may be used alone or in combination of two or more.

  In the resin composition layer constituting the interlayer film for laminated glass of the present invention, the alkali metal salt / alkaline earth metal salt (E) is 0.0001 to in terms of metal with respect to 100 parts by weight of the polyvinyl acetal (A). It is preferable to contain 0.04 weight part. If the amount is less than 0.0001 part by weight, the effect of controlling the adhesive force or the resin pH may not be obtained. More preferably, it is 0.001 part by weight or more. Moreover, when it exceeds 0.04 weight part, aggregation of the heat ray shielding fine particle surface-treated with the organosilicon compound is accelerated | stimulated, and there exists a possibility that the transparency of a laminated glass may be lost as a result. More preferably, it is 0.025 weight part or less, More preferably, it is 0.02 weight part or less.

  The resin composition layer constituting the interlayer film for laminated glass of the present invention comprises a heat ray shielding fine particle (C) and an alkali metal salt and / or an alkaline earth metal salt (E) with respect to polyvinyl acetal (A). , Obtained separately by melt-molding. The heat ray shielding fine particles (C) in the resin composition layer can be obtained by separately adding the heat ray shielding fine particles (C) and the alkali metal salt and / or alkaline earth metal salt (E) to the polyvinyl acetal (A). As a result, a film having a low haze can be obtained.

  The mixing method is not particularly limited as long as the heat ray shielding fine particles (C) and the alkali metal salt and / or alkaline earth metal salt (E) can be added separately. For example, a method of separately mixing heat ray shielding fine particles (C) and alkali metal salt and / or alkaline earth metal salt (E) into polyvinyl acetal (A), dispersion of heat ray shielding fine particles (C) (d1) and , A method of separately mixing a dispersion (d2) of an alkali metal salt and / or an alkaline earth metal salt (E) into the polyvinyl acetal (A), molding of the polyvinyl acetal (A) containing the heat ray shielding fine particles (C) Body, and dispersion method (d2) of alkali metal salt and / or alkaline earth metal salt (E) separately in polyvinyl acetal (A), alkali metal salt and / or alkaline earth metal salt (E) And the like, and a method of separately mixing a molded product of polyvinyl acetal (A) containing a dispersion of heat ray shielding fine particles (C) (d1) into polyvinyl acetal (A). That. Among these, the dispersion (d1) of the heat ray shielding fine particles (C) and the dispersion (d2) of the alkali metal salt and / or alkaline earth metal salt (E) are separately mixed in the polyvinyl acetal (A). It is preferable to do. Here, the order in which the dispersion liquid (d1), the dispersion liquid (d2), the plasticizer (B), and the polyvinyl acetal (A) are melt mixed is not particularly limited.

  The solvent contained in the dispersion (d1) is not particularly limited, and a general-purpose organic solvent, water, a plasticizer, or the like can be used. Examples of general-purpose organic solvents include methanol, ethanol, n-propanol, i-propanol, n-butanol, ethylene glycol, diethylene glycol, hexylene glycol, tetrahydrofuran, dioxane, acetone, methyl ethyl ketone, γ-butyrolactone, ε-caprolactone, N -Methylpyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, hexane, toluene, acetonitrile and the like.

  Further, the solvent contained in the dispersion liquid (d2) is not particularly limited, and the same solvent as the dispersion liquid (d1) can be used as a dispersion medium, but in particular, alkali metal salts and / or alkaline earths. It is preferable that the aqueous solution of the metal salt is suspended in the plasticizer.

  In order to finely disperse the heat ray shielding fine particles (C) in the resin composition layer, it is preferable that they are finely dispersed in the dispersion liquid (d1). For example, it is preferable to perform an operation of mechanically pulverizing the dispersion liquid (d1) of the heat ray shielding fine particles (C) from the viewpoint of reducing haze.

  Examples of the apparatus for pulverizing the heat ray shielding fine particles (C) in the dispersion include a sand mill, a ball mill, a jet mill, a homogenizer, an attritor, a paint shaker, a nanomizer, a high-speed stirrer, an ultrasonic disperser, and a bead mill. Using these apparatuses, the aggregates of the heat ray shielding fine particles (C) can be pulverized and dispersed. A bead mill is preferable in order to achieve a fine average particle diameter efficiently.

  When preparing the dispersion (d1), it is preferable to add a dispersant in advance in order to prevent re-aggregation of the pulverized particles. The dispersant to be used is not particularly limited, and those suitable for various conditions such as the type of heat ray shielding fine particles, the type of organosilicon compound, the surface fixing amount of the organosilicon compound, and the dispersion medium are used. Examples of such dispersants include amine dispersants, carboxylic acid dispersants, phosphate ester dispersants, sulfate ester dispersants, polyoxyethylene dispersants, alcohol dispersants, chelating agents, polyvinylpyrrolidone, PVA, polyvinyl butyral, etc. are mentioned. These may be used alone or in combination of two or more.

  The method for mixing the dispersion (d1), the dispersion (d2), the plasticizer (B), and the polyvinyl acetal (A) is not particularly limited, but it is preferable to mix by melt kneading from the viewpoint of productivity and the like. . It does not specifically limit as a kneading | mixing method, Well-known kneading machines, such as a single screw extruder, a twin screw extruder, a brabender, an open roll, a kneader, can be used.

  The mixed melt is melt-molded into a film to form a resin composition layer. A known method can be adopted as the molding method. A film can be produced by directly attaching a T-die to the melt-kneading apparatus, or a resin composition pellet can be produced once, and then a film can be separately formed. Although the film thickness of the film is not particularly limited, it is 0.2 to 1.2 mm, preferably 0.3 to 1.0 mm, considering the minimum penetration resistance and weather resistance required for laminated glass. is there.

  The interlayer film for laminated glass of the present invention may be composed of one resin composition layer as described above. The resin composition layer, polyvinyl acetal (A ′), plasticizer (B ′), and ultraviolet absorption And a second resin composition layer containing the agent (D). In this case, it is preferable that the resin composition layer (hereinafter sometimes referred to as the first resin composition layer) has a structure sandwiched between two second resin composition layers. By having the 2nd resin composition layer containing a ultraviolet absorber (D), deterioration of the resin in a 1st resin composition layer and a quality change of heat ray shielding particulates (C) can be controlled.

  At this time, the amount of the heat ray shielding fine particles (C) contained in the first resin composition layer is 100 parts by weight of the total amount of polyvinyl acetal and plasticizer contained in all the layers constituting the interlayer film for laminated glass. It is preferable that it is 0.001-2 weight part with respect to this.

  Further, an alkali metal salt and / or an alkaline earth metal salt may be added to the second resin composition layer. Thus, the amount of the alkali metal salt and / or alkaline earth metal salt of the first resin composition layer is reduced by imparting the adhesive force control function to the layer not containing the heat ray shielding fine particles (C). The aggregation of the heat ray shielding fine particles (C) can be reduced.

  As the polyvinyl acetal (A ′) and the plasticizer (B ′) contained in the second resin composition layer, the polyvinyl acetal (A) and the plasticizer (B) contained in the first resin composition layer The same can be used.

  In this case, it is preferable that the vinyl alcohol unit amount in polyvinyl acetal (A) is 22 mol% or less, 16.5-21 mol% is more preferable, 17-20 mol% is further more preferable. The amount of vinyl acetate units in the polyvinyl acetal (A) is preferably 5 to 8 mol%, more preferably 5 to 7.9 mol%, still more preferably 5 to 7.5 mol%, and 5.3 to 7. 2 mol% is most preferred. On the other hand, the vinyl alcohol unit amount in the polyvinyl acetal (A ′) is preferably 25 to 34 mol%, more preferably 27 to 32 mol%, and further preferably 29 to 31 mol%. The amount of vinyl acetate units in the polyvinyl acetal (A ′) is preferably 0.1 to 11 mol%, more preferably 0.1 to 4 mol%, and further preferably 0.1 to 2 mol%. When the molecular structure of the polyvinyl acetals (A) and (A ′) is in the above range, the sound insulation performance of the resulting interlayer film for laminated glass is improved.

  Here, the sound insulation performance is evaluated by the damping performance. That is, in a laminated glass produced by sandwiching and adhering an interlayer film for laminated glass between two 2 mm-thick clear glasses, the 1st mode damping performance at 20 ° C. when measured in accordance with ISO 16940 is 22% or more. It is also preferable that the damping performance of the 1st mode at 10 ° C. is 10% or more.

  In the interlayer film for laminated glass of the present invention, sound insulation performance can be imparted while maintaining the mechanical strength by introducing a soft layer. For example, when the difference between the content of the plasticizer contained in the first resin composition layer and the content of the plasticizer contained in the second resin composition layer is 5% by weight or more, The layer containing many becomes a soft layer, and the sound insulation performance is exhibited. The difference in the plasticizer content is preferably 7.5% by weight or more, and more preferably 10% by weight or more.

  The ultraviolet absorber (D) contained in the second resin composition layer is not particularly limited. Benzotriazole UV absorbers, triazine UV absorbers such as Tinvain 1577 manufactured by Ciba Japan, benzophenone UV absorbers such as CHIMASSORB 81 manufactured by Ciba Japan, and malonate UV absorbers such as Hostavin PR-25 manufactured by Clariant An agent etc. are mentioned, These may be used independently and may use 2 or more types together. Moreover, you may use together well-known light stabilizers, such as a hindered amine type compound, with these ultraviolet absorbers.

  Although it does not specifically limit as the addition amount of the said ultraviolet absorber (D) in a 2nd resin composition layer, With respect to 100 weight part of resin compositions which consist of a polyvinyl acetal (A ') and a plasticizer (B'), It is preferable that it is 0.01-10 weight part. When the addition amount is less than 0.01 parts by weight, the ultraviolet shielding effect may not be expected. A more preferable addition amount is 0.05 parts by weight or more, and further preferably 0.1 parts by weight or more. Moreover, when the addition amount exceeds 10 parts by weight, the coloring of the interlayer film may be remarkable. A more preferable addition amount is 5 parts by weight or less, and further preferably 2 parts by weight or less.

  As a method for producing an interlayer film for laminated glass having a plurality of layers, a general method for forming a multilayer film can be applied. That is, a method in which the resin composition of each layer is coextruded to a die or a feed block, a method in which each layer is formed into a film separately, and a method of laminating the layers after that is then included.

  The interlayer film for laminated glass of the present invention is preferably a laminated glass produced by sandwiching and adhering two 2 mm thick clear glasses, and the haze measured according to JIS K7105 is preferably 2% or less.

  In the interlayer film for laminated glass of the present invention, various additives such as antioxidants, stabilizers, lubricants, flame retardants, processing aids, antistatic agents, and the like as long as they do not inhibit the effects of the invention, Coloring agents, heat ray reflective agents, heat ray absorbers, impact resistance aids, fillers, moisture resistance agents, and the like may be added.

  A laminated glass is produced using the interlayer film for laminated glass of the present invention thus obtained. The glass to be used is not particularly limited, and those generally used can be used, and examples thereof include float plate glass, polished plate glass, template glass, netted glass, lined glass, colored glass, and heat ray absorbing glass. . In addition to inorganic glass, polycarbonate, polymethyl methacrylate, or the like having excellent transparency may be used. It does not specifically limit as a method to manufacture the laminated glass of this invention, A conventionally well-known method can be used. Specifically, a laminated glass is produced by sandwiching an intermediate film between at least two glass plates, heating and melting, and then cooling and solidifying.

  The interlayer film for laminated glass of the present invention is excellent in transparency, adhesiveness, durability and heat ray shielding properties. Therefore, the laminated glass obtained by laminating this with glass can be widely used as window materials for buildings, vehicles, aircraft, ships, and the like. Examples of vehicles in which laminated glass is used include automobiles and trains. In automobiles, the laminated glass of the present invention can be used as a windshield, side glass, rear glass, roof glass, and the like.

  EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, this invention is not limited at all by these Examples. In the following examples and comparative examples, each evaluation value was measured and calculated according to the following method.

[Organic silicon compound fixing amount]
Using the fluorescent X-ray analyzer “RIX3100” manufactured by Rigaku Denki Kogyo Co., Ltd., the heat ray shielding fine particles produced were measured for the silicon atom abundance (% by weight of the fine particles based on solid content). Then, the fixing amount of the organosilicon compound (% by weight with respect to the solid content of the fine particles) was calculated according to the following formula (III).

Fixing amount = Abundance of Si atoms in the particle × (SiO ₂ R molecular weight / Si atomic weight)
… (III)

However, in formula (III), R represents the substituent which has a covalent bond with silicon atoms other than an alkoxy group in the molecule | numerator of the said organosilicon compound.

[Visible light transmittance and solar radiation transmittance]
Using a spectrophotometer “SolidSpec-3700” manufactured by Shimadzu Corporation, the transmittance in the wavelength region of 280 to 2500 nm was measured for the produced laminated glass. And according to JIS R3106, the visible light transmittance | permeability (%) of 380-780 nm was calculated | required. Moreover, the solar radiation transmittance (%) of 300-2500 nm was calculated | required using the weight value coefficient of JISR3106.

[Haze]
Using a turbidimeter “NDH-5000” manufactured by Nippon Denshoku Industries Co., Ltd., the haze (%) was measured according to JIS K7105 for the produced laminated glass.

[Light resistance]
For the light resistance evaluation, a light resistance tester “Due Panel Light Control Weather Meter FDP” manufactured by Suga Test Instruments Co., Ltd. was used. The obtained laminated glass was irradiated with UV light at an intensity of 30 W / m ² for 200 hours, and the difference (ΔTL) in visible light transmittance before and after irradiation was calculated as an index of light resistance.

[Preparation of surface-treated heat-shielding fine particles]
In a 60 wt% methanol dispersion of ZnSb ₂ O ₆ (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.), 5 parts by weight of phenyltrimethoxy with respect to 100 parts by weight of anhydrous zinc antimonate Silane (“KBM-103” manufactured by Shin-Etsu Chemical Co., Ltd.) and water were added and heated to reflux for 5 hours. The dispersion was concentrated with an evaporator to obtain a dry powder, and then calcined at 200 ° C. for 2 hours. Thereafter, the obtained powder was washed with methanol and acetone, and unreacted substances were eluted and removed to obtain a surface-treated zinc antimonate powder. The fixed amount of the organosilicon compound of the surface-treated zinc antimonate powder was determined by the above method. The results are shown in Table 1.

[Preparation of interlayer film for laminated glass]
Methanol was added to the prepared surface-treated zinc antimonate powder and pulverized with a bead mill to prepare a surface-treated zinc antimonate methanol dispersion (d0) having a concentration of 10% by weight. 1.6 g of the resulting dispersion (d0), 0.16 g of a surfactant “Plysurf A208F” manufactured by Daiichi Kogyo Seiyaku Co., Ltd., triethylene glycol di (2-ethylhexanoate) (hereinafter abbreviated as 3G8) as a plasticizer ) Dispersion (d1) obtained by mixing 5.2 g, 10 g of 3G8, 0.14 g of “Tinuvin 328” manufactured by Ciba Japan as an ultraviolet absorber, magnesium acetate and potassium acetate as an adhesion control agent Dispersions (d2) obtained by mixing 0.08 g of a 25 wt% aqueous solution of a mixture (mixing weight ratio: 2/1) were separately obtained from polyvinyl butyral (raw material PVA viscosity average polymerization degree 1700, acetalization degree 70). (Mol%, vinyl alcohol unit amount 29 mol%, vinyl acetate unit amount 1 mol%) was added to 40 g and mixed. This mixture was kneaded at 170 ° C. with a lab plast mill, and then press molded at 140 ° C. for 5 minutes with a press machine to produce a 0.76 mm thick interlayer film for laminated glass. Table 2 shows the structure of the intermediate film.

[Production and evaluation of laminated glass]
The obtained interlayer film for laminated glass was sandwiched between two pieces of 2 mm-thick glass (Saint Gobain, Planilux Clear), and then held at 140 ° C. under reduced pressure for 90 minutes to produce a laminated glass. . The obtained laminated glass was evaluated by the above method. The results are shown in Table 3.

  In Example 1, when producing the surface-treated zinc antimonate powder, a surface-treated zinc antimonate powder was obtained in the same manner as in Example 1 except that the amount of phenyltrimethoxysilane used was 10 parts by weight. . Thereafter, an interlayer film for laminated glass and a laminated glass were produced and evaluated in the same manner as in Example 1. The results are shown in Tables 1-3.

  In Example 1, a surface-treated zinc antimonate powder was obtained in the same manner as in Example 1 except that hexyltrimethoxysilane was used as the silicon compound to be added when producing the surface-treated zinc antimonate powder. Thereafter, an interlayer film for laminated glass and a laminated glass were produced and evaluated in the same manner as in Example 1. The results are shown in Tables 1-3.

  In Example 1, instead of the dispersion liquid (d1), 8.0 g of the dispersion liquid (d0), 0.8 g of surfactant “Plysurf A208F” manufactured by Daiichi Kogyo Seiyaku Co., Ltd., and 3G8 5.2 g are mixed. An interlayer film layer x for laminated glass having a thickness of 0.16 mm was produced in the same manner as in Example 1 except that the obtained dispersion liquid (d1 ′) was used. Next, 15.2 g of 3G8, 0.14 g of “Tinvin 328” as an ultraviolet absorber, and 0.08 g of a 25 wt% aqueous solution of a mixture of magnesium acetate and potassium acetate (mixing weight ratio: 2/1) are the same as above. After adding to 40 g of polyvinyl butyral and mixing, an interlayer film layer y for laminated glass having a thickness of 0.3 mm was produced in the same manner as in Example 1. Further, the produced layer x was sandwiched between two layers y, and thereafter, a laminated glass was produced in the same manner as in Example 1. The obtained laminated glass was evaluated by the above method. The results are shown in Table 3.

19.9 g of 3G8, 0.08 g of 25 wt% aqueous solution of a mixture of magnesium acetate and potassium acetate (mixing weight ratio: 2/1) was added to polyvinyl butyral (raw material PVA viscosity average polymerization degree 1700, acetalization degree 74 mol% And 35.3 g of vinyl alcohol unit amount 19 mol%, vinyl acetate unit amount 7 mol%). This mixture was kneaded at 170 ° C. with a lab plast mill, and then press molded at 140 ° C. for 5 minutes with a press machine to produce an interlayer film x for laminated glass having a thickness of 0.16 mm. Next, in Example 1, instead of the dispersion liquid (d1), a dispersion liquid (d1 ″) obtained by mixing 2.0 g of the dispersion liquid (d0), 0.2 g of phosphate ester, and 5.2 g of 3G8. The intermediate film layer y for laminated glass having a thickness of 0.3 mm was produced in the same manner as in Example 1, except that the layer x was sandwiched between two layers y. A laminated glass was produced in the same manner as in 1. The obtained laminated glass was evaluated by the above method, and the results are shown in Table 3.
Moreover, as a result of evaluating the damping performance of the 1st mode (179 Hz) at 10 ° C. according to ISO 16940, the laminated glass was found to have a damping performance of 11%. Further, the damping performance in the 1st mode (128 Hz) at 20 ° C. was 23%.

In Example 4, the addition amount of polyvinyl butyral contained in the layer x (viscosity average polymerization degree of raw material PVA 1700, acetalization degree 74 mol%, vinyl alcohol unit amount 19 mol%, vinyl acetate unit amount 7 mol%) was 35. 3 g, the amount of 3G8 contained in d1 ′ was 9.9 g, the amount of 3G8 contained in d2 was 10 g, and this mixture was kneaded at 100 ° C. with a lab plast mill, as in Example 1. A sample was prepared. The obtained laminated glass was evaluated by the above method. The results are shown in Table 3.
Moreover, as a result of evaluating the damping performance of the 1st mode (179 Hz) at 10 ° C. according to ISO 16940, the laminated glass was found to have a damping performance of 11%. Further, the damping performance in the 1st mode (128 Hz) at 20 ° C. was 23%.

Comparative Example 1
In Example 1, an interlayer film for laminated glass and a laminated glass were prepared and evaluated in the same manner as in Example 1 except that the surface-treated zinc antimonate methanol dispersion (d0) was not used. The results are shown in Tables 1-3.

Comparative Example 2
In Example 1, instead of the surface-treated zinc antimonate methanol dispersion (d0), a 60 wt% methanol dispersion of anhydrous zinc antimonate (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill. Then, an interlayer film for laminated glass and a laminated glass were prepared and evaluated in the same manner as in Example 1 except that 0.27 g of the finely divided anhydrous zinc antimonate dispersion (60 wt% methanol dispersion) was used. The results are shown in Tables 1-3.

Comparative Example 3
In Example 1, 10 g of the dispersion liquid (d1), 0.14 g of “Tinuvin 328” as an ultraviolet absorber, and a mixture of magnesium acetate and potassium acetate as an adhesion control agent (mixing weight ratio: 2/1) An interlayer film for laminated glass and a laminated glass were prepared and evaluated in the same manner as in Example 1 except that 0.32 g of a 25% by weight aqueous solution was previously mixed and then added to polyvinyl butyral at the same time. The results are shown in Tables 1-3.

  From the results shown in Table 3, the laminated glass (Examples 1 to 6) using the interlayer film for laminated glass of the present invention suppresses the solar transmittance while maintaining a high visible light transmittance, and is irradiated with high energy rays. It can be seen that there is little deterioration of the haze and there is almost no haze even when an adhesive strength control agent is added. When it does not contain the heat ray shielding fine particles (C) (Comparative Example 1), the heat ray shielding performance is not sufficient. When the heat ray shielding fine particles are not surface-treated with the organosilicon compound (Comparative Example 2), the deterioration under high energy ray irradiation is remarkable. When heat ray shielding fine particles (C) surface-treated with an alkali metal / alkaline earth metal and an organosilicon compound are added in advance (Comparative Example 3), aggregation of the surface-treated heat ray shielding fine particles (C) is promoted. As a result, the haze cannot be kept low, and the visible light transmittance is reduced.

  ADVANTAGE OF THE INVENTION According to this invention, the intermediate film for laminated glasses which can shield a heat ray efficiently, maintaining the transparency and adhesiveness, and was excellent in durability can be provided. Laminated glass using the interlayer film for laminated glass can be suitably used for, for example, automotive windshield, side glass, rear glass, roof glass, glass parts of vehicles such as aircraft and trains, architectural glass, etc. By suppressing the rise, it is possible to reduce the use of excessive cooling equipment and enable environmentally friendly space design.

Claims (18)

  Polyvinyl acetal (A), plasticizer (B), heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent, and alkali metal salt and / or alkaline earth metal salt (E) An interlayer film for laminated glass comprising at least one resin composition layer containing the resin composition layer, wherein the resin composition layer is surfaced with an organosilicon compound having a hydrolyzable substituent with respect to polyvinyl acetal (A). The heat-shielding fine particles (C) thus treated and the alkali metal salt and / or alkaline earth metal salt (E) are separately mixed and then melt-molded, and further, polyvinyl acetal ( A ′), a plasticizer (B ′), and a second resin composition layer containing an ultraviolet absorber (D), the content of the plasticizer contained in the resin composition layer, The interlayer film for a laminated glass, wherein the difference in the content of the plasticizer contained in the second resin composition layer is 5 wt% or more. The resin composition layer is a dispersion (d1) of heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent with respect to polyvinyl acetal (A), an alkali metal salt, and / or The interlayer film for laminated glass according to claim 1, wherein the interlayer film is obtained by melt-molding the dispersion (d2) of the alkaline earth metal salt (E) separately and then melt-molding. The interlayer film for laminated glass according to claim 2, wherein the dispersion (d1) has been subjected to a wet pulverization treatment. The said resin composition layer contains 0.0001-0.04 weight part of metal conversion of an alkali metal salt and / or alkaline-earth metal salt (E) with respect to 100 weight part of polyvinyl acetal (A). The interlayer film for laminated glass according to any one of 1 to 3. Heat-shielding fine particles (C) 0 in which the resin composition layer is surface-treated with an organosilicon compound having a hydrolyzable substituent with respect to 100 parts by weight of the total amount of polyvinyl acetal (A) and plasticizer (B). The interlayer film for laminated glass according to any one of claims 1 to 4, comprising 0.001 to 2 parts by weight. The heat ray shielding fine particles (C) are tin-doped indium oxide, antimony-doped tin oxide, aluminum-doped zinc oxide, indium-doped zinc oxide, gallium-doped zinc oxide, tungsten oxide, lanthanum hexaboride, cerium hexaboride, anhydrous antimonic acid The interlayer film for laminated glass according to any one of claims 1 to 5, which is at least one selected from the group consisting of zinc and copper sulfide. The interlayer film for laminated glass according to claim 6, wherein the heat ray shielding fine particles (C) are anhydrous zinc antimonate. The interlayer film for laminated glass according to any one of claims 1 to 7 , wherein the resin composition layer has a structure sandwiched between two second resin composition layers. In the laminated glass produced by sandwiching and bonding the interlayer film for laminated glass between two 2 mm thick clear glasses, the 1st mode damping performance at 20 ° C. when measured according to ISO 16940 is 22% or more. The interlayer film for laminated glass according to any one of claims 1 to 8. In the laminated glass produced by sandwiching and bonding the interlayer film for laminated glass between two 2 mm thick clear glasses, the 1st mode damping performance at 10 ° C. when measured according to ISO 16940 is 10% or more. The interlayer film for laminated glass according to any one of claims 1 to 9. In the polyvinyl acetal (A), the vinyl alcohol unit amount is 22 mol% or less, the vinyl acetate unit amount is 5 to 8 mol%, the vinyl alcohol unit amount in the polyvinyl acetal (A ′) is 25 to 34 mol%, vinyl The interlayer film for laminated glass according to any one of claims 1 to 10, wherein the acetate unit amount is 0.1 to 11 mol%. The laminated glass produced by sandwiching and bonding the interlayer film for laminated glass between two 2 mm-thick clear glasses, and having a haze measured according to JIS K7105 of 2% or less, according to any one of claims 1 to 11. The interlayer film for laminated glass described. The laminated glass formed by adhere | attaching a several glass plate using the intermediate film for laminated glasses in any one of Claims 1-12. A step of melt-mixing the dispersion (d1) of the heat ray shielding fine particles (C) surface-treated with the organosilicon compound having a hydrolyzable substituent and the plasticizer (B) with the polyvinyl acetal (A) to form a film. The manufacturing method of the intermediate film for laminated glasses in any one of Claims 1-12 containing this. A dispersion (d1) of heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent, and an alkali metal salt and / or alkaline earth metal salt (E) are separately obtained from polyvinyl acetal. The manufacturing method of the intermediate film for laminated glasses of Claim 14 including the process of melt-molding in a film form after mixing with (A). A dispersion (d1) of heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent, and a dispersion (d2) of an alkali metal salt and / or alkaline earth metal salt (E) The method for producing an interlayer film for laminated glass according to claim 14, comprising a step of separately mixing with polyvinyl acetal (A) and then melt-molding it into a film. The process of preparing the heat ray shielding fine particle (C) by which the surface treatment was carried out by baking the mixture of the organosilicon compound which has a hydrolyzable substituent, and a heat ray shielding fine particle at 100-400 degreeC. A method for producing an interlayer film for laminated glass according to claim 1. The method includes the step of preparing a dispersion (d1) of heat ray shielding fine particles (C) by pulverizing the heat ray shielding fine particles (C) surface-treated with an organosilicon compound having a hydrolyzable substituent. The manufacturing method of the intermediate film for laminated glasses in any one of 14-17.