JP2003327454A - Intermediate film for laminated glass and laminated glass - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an intermediate film for laminated glass which is excellent in transparency and mechanical strength in making the laminated glass and does not impair initial optical quality even after a durability test and laminated glass formed by using such intermediate film for the laminated glass. <P>SOLUTION: The intermediate film for the laminated glass contains a polyvinyl acetal resin, UV absorbent, plasticizer, adhesive strength regulating agent, and antioxidant, in which the UV absorbent is a malonic ester compound and/or anilide oxalate component. <P>COPYRIGHT: (C)2004,JPO

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to an interlayer film for laminated glass, which has excellent transparency and mechanical strength when formed into laminated glass, and which does not impair the initial optical quality even after a durability test, and this laminated glass. The present invention relates to a laminated glass using an intermediate film.

[0002]

2. Description of the Related Art Conventionally, laminated glass is safe because it is less likely to cause glass fragments to scatter even if it is damaged by an external impact, so that it is used as a window glass for vehicles such as automobiles, aircraft and buildings. Widely used. As the laminated glass, for example, an interlayer film for laminated glass (hereinafter, also referred to as an interlayer film) made of a polyvinyl acetal resin such as a polyvinyl butyral resin plasticized with a plasticizer is interposed between at least a pair of glasses, and integrated. And the like.

However, the laminated glass using such an intermediate film is excellent in basic performance such as safety,
It was inferior in moisture resistance and weather resistance such as durability against heat and light. If the humidity resistance is poor, in an atmosphere of high humidity, since the intermediate film and the air are in direct contact with each other at the peripheral edge of the laminated glass, the intermediate film in the peripheral part is whitened and the adhesiveness between the intermediate film and the glass, There arises a problem that optical quality characteristics such as mechanical strength, transparency and visible light transmittance are deteriorated. On the other hand, JP-A-7-41340 discloses a technique for reducing whitening after a humidity resistance test.

When the durability against heat and light is poor, sunlight is composed of light of various wavelength components even when used for ordinary daylight, and also includes light of high energy short wavelength components such as ultraviolet rays. Therefore, there is a problem that the intermediate film is deteriorated by repeated irradiation of sunlight and characteristics such as mechanical strength and adhesiveness are deteriorated. On the other hand, generally, a method of improving light resistance by incorporating an ultraviolet absorber or the like into the interlayer film is adopted, but deterioration of optical quality characteristics such as visible light transmittance due to heat or light is deteriorated. Was not sufficiently suppressed, and there was a proportional relationship between the durability test time and the deterioration of visible light transmittance. When using laminated glass as a windshield for automobiles, for example, it is important that the visible light transmittance does not change particularly in the durability test because there is a lower limit regulation of the visible light transmittance legally. The laminated glass using the above intermediate film has a problem that durability of optical quality such as visible light transmittance is not sufficient.

[0005]

DISCLOSURE OF THE INVENTION The present invention provides an interlayer film for laminated glass, which has excellent transparency and mechanical strength when formed into laminated glass, and which does not impair the initial optical quality even after a durability test, and The present invention provides a laminated glass using an interlayer film for laminated glass.

[0006]

Means for Solving the Problems As a result of intensive studies, the present inventors have found that absorption of conventional ultraviolet absorbers such as benzotriazole compounds generally used in the intermediate film affects the visible light region. That the interlayer film is already colored yellow when added; the conventional UV absorber has a functional group such as a reactive phenolic OH group. It becomes a factor of complex formation with heavy metals such as magnesium used in the process, and the complex is colored yellow to reduce the visible light transmittance; conventional UV absorbers greatly affect the durability of interlayer films. It was found that the resin matrix is oxidized by heat or energy such as light (especially in the ultraviolet range), and further, an ultraviolet absorber capable of solving these problems was found, and the present invention was completed. This has led to the.

The present invention is an interlayer film for laminated glass, which comprises a polyvinyl acetal resin, an ultraviolet absorber, a plasticizer, an adhesive strength adjusting agent, and an antioxidant, wherein the ultraviolet absorber is a malonic ester type. It is an intermediate film for laminated glass which is a compound and / or an oxalic acid anilide compound. The details of the present invention are shown below.

The interlayer film for laminated glass (hereinafter, also referred to as an interlayer film) of the present invention contains a polyvinyl acetal resin, an ultraviolet absorber, a plasticizer, an adhesive strength modifier, and an antioxidant. The polyvinyl acetal resin is not particularly limited, but for example, polyvinyl butyral resin is preferably used. The polyvinyl acetal resin may be blended in an appropriate combination according to the required physical properties, and is a co-polyvinyl acetal resin obtained by acetalizing by combining aldehydes during acetalization. May be. The molecular weight and molecular weight distribution of the polyvinyl acetal resin are not particularly limited, but the degree of acetalization is generally 40 to 85.
%, With a preferable lower limit of 60% and an upper limit of 75%.

The above polyvinyl acetal resin can be obtained by acetalizing polyvinyl alcohol with an aldehyde. The polyvinyl alcohol is usually obtained by saponifying polyvinyl acetate,
Polyvinyl alcohol having a saponification degree of 80 to 99.8 mol% is generally used. The preferred lower limit of the viscosity average polymerization degree of the polyvinyl alcohol resin is 200, and the upper limit thereof is 300.
It is 0. If it is less than 200, the penetration resistance of the obtained laminated glass will be reduced, and if it exceeds 3000, the moldability of the resin film will be poor, the rigidity of the resin film will be too large, and the processability will be poor. A more preferred lower limit is 500 and an upper limit is 20.
00. The viscosity average degree of polymerization and the degree of saponification of the polyvinyl alcohol resin are, for example, JIS K 6726.
It can be measured based on the “polyvinyl alcohol test method”.

The aldehyde is not particularly limited,
Generally, an aldehyde having 1 to 10 carbon atoms is used.
Specifically, for example, n-butyraldehyde, isobutyraldehyde, n-valeraldehyde, 2-ethylbutyraldehyde, n-hexylaldehyde, n-octylaldehyde, n-nonylaldehyde, n-decylaldehyde, formaldehyde, acetaldehyde, Examples thereof include benzaldehyde. Among them, n-butyraldehyde, n-hexylaldehyde and n-valeraldehyde are preferably used. Particularly preferred is butyraldehyde having 4 carbon atoms.

The ultraviolet absorber is a malonic acid ester-based compound and / or an oxalic acid anilide-based compound. The malonate compound is not particularly limited,
For example, malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Ho
Stavin PR-25) and the like. The oxalic acid anilide compound is not particularly limited, and examples thereof include 2-ethyl 2′-ethoxy-oxalanilide (C
and Sanduvor VSU manufactured by Lariant Inc., and the like.

As the ultraviolet absorber, the malonic acid ester compound and / or oxalic acid anilide compound and the conventionally used benzotriazole compound, benzophenone compound, triazine compound, benzoate compound, and , And at least one selected from the group consisting of hindered amine compounds may be used in combination.

The benzotriazole-based compound is not particularly limited, and may be, for example, 2- (2'-hydroxy-).
5'-Methylphenyl) benzotriazole (Tinuvin P, manufactured by Ciba-Geigy), 2- (2'-hydroxy-3 ', 5'-di-t-butylphenyl) benzotriazole (manufactured by Ciba-Geigy, Tinuvin32)
0), 2- (2'-hydroxy-3'-t-butyl-
5'-methylphenyl) -5-chlorobenzotriazole (Tinuvin 326, manufactured by Ciba-Geigy), 2-
(2'-hydroxy-3 ', 5'-di-amylphenyl) benzotriazole (Ciba Geigy, Tinu
Vin 328) and the like.

The benzophenone compound is not particularly limited, and examples thereof include octabenzone (Chimassorb 81, manufactured by Ciba-Geigy). The triazine-based compound is not particularly limited, for example,
2- (4,6-diphenyl-1,3,5-triazine-
2-yl) -5-[(hexyl) oxy] -phenol (Tinuvin 1577FF manufactured by Ciba-Geigy) and the like can be mentioned. The benzoate compound is not particularly limited, and for example, 2,4-di-tert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate (Tinuvin1 manufactured by Ciba-Geigy).
20) and the like. The hindered amine compound is not particularly limited, and examples thereof include LA-57 (manufactured by ADEKA ARGUS CORPORATION).

The lower limit of the preferred content of the above-mentioned ultraviolet absorber is 0.1% with respect to 100 parts by weight of the polyvinyl acetal resin.
01 parts by weight, the upper limit is 5.0 parts by weight. If it is less than 0.01 part by weight, the effect of absorbing ultraviolet rays is hardly obtained. If it exceeds 5.0 parts by weight, the weather resistance of the resin may deteriorate. A more preferable lower limit is 0.05 part by weight,
The upper limit is 1.0 part by weight.

The above-mentioned plasticizer is not particularly limited as long as it is usually used for polyvinyl acetal resin, and known plasticizers generally used as a plasticizer for an intermediate film can be mentioned. Examples thereof include organic plasticizers such as basic organic acid esters and polybasic organic acid esters; phosphoric acid plasticizers such as organic phosphoric acid-based and organic phosphorous acid-based plasticizers. These plasticizers may be used alone or in combination of two or more, and are selected depending on the type of polyvinyl acetal resin in consideration of compatibility with the resin and the like.

The monobasic organic acid ester plasticizer is not particularly limited, and examples thereof include glycols such as triethylene glycol, tetraethylene glycol or tripropylene glycol, and butyric acid, isobutyric acid, caproic acid, 2-ethylbutyric acid. , Heptyl acid, n-octylic acid, 2
-Glycol-based esters obtained by reaction with a monobasic organic acid such as ethylhexyl acid, pelargonic acid (n-nonyl acid) or decyl acid. Among them, triethylene glycol-dicaproic acid ester, triethylene glycol-di-2-ethylbutyric acid ester, triethylene glycol-di-n-octyl acid ester, triethylene glycol-di-2-ethylhexyl acid ester, and other triethylenes. A monobasic organic acid ester of glycol is preferably used.

The polybasic organic acid ester plasticizer is not particularly limited, and examples thereof include polybasic organic acids such as adipic acid, sebacic acid or azelaic acid, and a carbon number of 4-8.
And an ester with a straight-chain or branched alcohol. Among them, dibutyl sebacate ester, dioctyl azelaate ester, dibutyl carbitol adipate ester and the like are preferably used.

The organic phosphoric acid-based plasticizer is not particularly limited, and examples thereof include tributoxyethyl phosphate, isodecylphenyl phosphate, triisopropyl phosphate and the like.

Specific examples of particularly preferable plasticizers include triethylene glycol-di-ethyl butyrate, triethylene glycol-di-ethylhexoate, and triethylene glycol di-butyl sebacate. .

The preferred lower limit of the content of the plasticizer is 20 parts by weight, and the upper limit thereof is 100 parts by weight, relative to 100 parts by weight of the polyvinyl acetal resin. If it is less than 20 parts by weight, the resulting laminated glass may have insufficient penetration resistance. If it exceeds 100 parts by weight, bleeding out of the plasticizer may occur, the transparency and adhesiveness of the interlayer film of the present invention may deteriorate, and the optical strain of the obtained laminated glass may increase. A more preferred lower limit is 30 parts by weight and an upper limit is 60 parts by weight.

The above-mentioned adhesive strength adjusting agent is not particularly limited, and examples thereof include alkali metal salts or alkaline earth metal salts of organic acids or inorganic acids, modified silicone oil and the like. The organic acid is not particularly limited, and examples thereof include carboxylic acids such as octylic acid, hexylic acid, butyric acid, acetic acid, and formic acid. The inorganic acid is not particularly limited,
Examples thereof include hydrochloric acid and nitric acid. The alkali metal salt and the alkaline earth metal salt are not particularly limited, and examples thereof include salts of potassium, sodium, magnesium and the like.

Among the above-mentioned alkali metal salts or alkaline earth metal salts of organic acids or inorganic acids, the alkali metal salts and alkaline earth metal salts of organic acids having 2 to 16 carbon atoms are preferable, and the carbon number is more preferable. The potassium and magnesium salts of 2 to 16 carboxylic acids.

The potassium salt and magnesium salt of the carboxylic acid having 2 to 16 carbon atoms are not particularly limited,
For example, magnesium acetate, potassium acetate, magnesium propionate, potassium propionate, magnesium 2-ethylbutanoate, potassium 2-ethylbutanoate, 2
-Magnesium ethylhexanoate, potassium 2-ethylhexanoate and the like are preferably used. These may be used alone or in combination of two or more.

In the case where the adhesive strength adjusting agent is an alkali metal salt or an alkaline earth metal salt of an organic acid or an inorganic acid, the preferable lower limit of the content of the adhesive strength adjusting agent is 0 based on 100 parts by weight of the polyvinyl acetal resin. 0.0001 parts by weight, the upper limit is 1.0 parts by weight. If the amount is less than 0.0001 part by weight, the adhesive force in the peripheral portion of the interlayer film may be reduced in a high humidity atmosphere. If it exceeds 1.0 part by weight, the adhesive strength may be too low and the transparency of the interlayer film may be lost. A more preferred lower limit is 0.001 part by weight, an upper limit is 0.5 part by weight, and a still more preferred lower limit is 0.01 part by weight and an upper limit is 0.2 part by weight.

The modified silicone oil is not particularly limited, and examples thereof include epoxy modified silicone oil, ether modified silicone oil, ester modified silicone oil, amine modified silicone oil, and carboxyl modified silicone oil. These may be used alone or in combination of two or more. These modified silicone oils are generally obtained by reacting a polysiloxane with a compound to be modified.

The preferred lower limit of the molecular weight of the modified silicone oil is 800, and the upper limit thereof is 5000. If it is less than 800, the localization on the surface of the interlayer film may be insufficient. If it exceeds 5,000, the compatibility with the resin may be reduced, and the film may bleed out to reduce the adhesive force with the glass. More preferable lower limit is 1500 and upper limit is 40.
00.

When the above-mentioned adhesion control agent is a modified silicone oil, the preferable lower limit of the content of the adhesion control agent is 0.01 parts by weight, and the upper limit is 0.2 parts by weight, relative to 100 parts by weight of the polyvinyl acetal resin. Is. 0.01
If it is less than the weight part, the effect of preventing whitening due to moisture absorption may be insufficient. If it exceeds 0.2 parts by weight, the compatibility with the resin may decrease, and bleeding out may occur on the film surface, resulting in a decrease in the adhesive force between the resin and the glass. A more preferred lower limit is 0.03 part by weight and an upper limit is 0.1 part by weight.

The above-mentioned antioxidant is used for preventing deterioration of the interlayer film composition due to heat in the extruder. The antioxidant is not particularly limited, and examples of the phenol-based antioxidant include 2,6-di-tert-butyl-
P-Cresol (BHT) (Sumitomo Chemical Co., Ltd., Sumirider BHT), tetrakis- [methylene-3- (3'-
5′-di-t-butyl-4′-hydroxyphenyl) propionate] methane (manufactured by Ciba-Geigy, Irganox 1010) and the like. The preferable lower limit of the content of the antioxidant is 0.01 parts by weight, and the upper limit thereof is 5.0 parts by weight.

The interlayer film of the present invention may further contain additives such as a light stabilizer, a surfactant, a flame retardant, an antistatic agent, a moisture resistance agent, a heat ray reflector and a heat ray absorber, if necessary. Good. The surfactant is not particularly limited, and examples thereof include sodium laurate and alkylbenzene sulfonic acid.

The thickness of the intermediate film of the present invention is not particularly limited, but the preferable lower limit is 0.3 mm and the upper limit is 0.8 mm in view of the minimum penetration resistance and weather resistance required for laminated glass. However, the interlayer film of the present invention and the interlayer film other than the above may be laminated and used according to need such as improvement of penetration resistance.

The method of forming the intermediate film of the present invention is not particularly limited, and examples thereof include a method of forming a film in a sheet form by an ordinary film forming method such as an extrusion method, a calendar method, a pressing method. Among them, the extrusion method in which the two axes are in the same direction is preferable, and the haze can be further improved.

In the interlayer film of the present invention, the malonic acid type compound and / or the oxalic acid anilide type compound are contained in the UV-B region by containing the malonic acid type compound and / or the oxalic acid anilide type compound as an ultraviolet absorber. Since it exhibits strong absorption, it causes deterioration of various resins 300
It is suitable for protecting the resin from ultraviolet rays having a wavelength of ˜320 nm, and can improve weather resistance and light resistance.
Moreover, since the absorption regions of the malonic acid-based compound and the oxalic acid anilide-based compound do not overlap with visible light, coloring does not occur. Furthermore, since the molar absorptivity is very high and the molecular weight is small, the amount of UV absorption at the same content is much higher than that of conventional UV absorbers, and it is possible to reduce the content of UV absorbers and reduce costs. it can. Since the malonic acid-based compound and the oxalic acid anilide-based compound do not have a functional group such as an OH group which may be a factor for complex formation with a heavy metal, even if a metal such as magnesium is contained in the interlayer film of the present invention. In addition, a complex is not formed by mixing during production or energy application in a durability test, yellowing or yellowing due to complex formation hardly occurs, and a decrease in visible light transmittance can be suppressed.

The interlayer film of the present invention contains a malonic acid type compound and / or an oxalic acid anilide type compound, which are ultraviolet absorbers, and therefore has excellent weather resistance, and has excellent transparency when formed into a laminated glass. It is possible to provide a laminated glass which has excellent mechanical strength and does not impair the initial optical quality even after the durability test.

The composition constituting the interlayer film of the present invention can be used for laminating transparent plastics such as polycarbonate and polymethylmethacrylate in addition to glass. It is also possible to apply it to a damping material by laminating it with a rigid body other than glass, such as a metal or an inorganic material.

A laminated glass using the interlayer film of the present invention is also one of the present invention. The glass used for the laminated glass of the present invention is not particularly limited, and examples thereof include commonly used transparent plate glass and the like.

The use of the laminated glass of the present invention is not particularly limited, and examples thereof include windshields and side glasses of automobiles, glass parts of vehicles such as aircraft and trains, and architectural glass. Further, it is also possible to use it as a functional laminated glass having a multilayer interlayer film in which an interlayer film such as a multilayer sound insulating interlayer film has a multilayer structure.

The laminated glass of the present invention is excellent in transparency and mechanical properties by using the interlayer film of the present invention,
Moreover, it does not impair the initial optical quality, especially the visible light transmittance even after the durability test.

[0039]

The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples.

Example 1 (1) Synthesis of polyvinyl butyral In 2890 g of pure water, an average degree of polymerization of 1700 and a degree of saponification of 99.
275 g of 2 mol% polyvinyl alcohol was added and dissolved by heating. The temperature of this solution was adjusted to 15 ° C and the concentration was adjusted to 35
201% by weight of hydrochloric acid and 157 g of n-butyraldehyde
Was added to maintain the temperature of 15 ° C. to precipitate the reaction product. Then, the reaction system is kept at 60 ° C. for 3 hours to complete the reaction, and then washed with excess water to wash off unreacted n-butyraldehyde, and the hydrochloric acid catalyst is used as a general-purpose neutralizing agent sodium hydroxide. The solution was neutralized with an aqueous solution, washed with excess water for 2 hours, and dried to obtain a white powdery polyvinyl butyral resin. The average degree of butyralization of this polyvinyl butyral resin was 68.5 mol%.

(2) Preparation of UV absorber and antioxidant mixed plasticizer Triethylene glycol-di-ethylene butyrate (3
GO) 40 parts by weight, 2,6-di-te as an antioxidant
rt-butyl-P-cresol (BHT) (Sumitomo Chemical Co., Ltd., Sumirider BHT) 0.2 part by weight, and malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (Clariant Co., Ltd.) as an ultraviolet absorber. Made by
0.2 parts by weight of Hostavin PR-25) was stirred and mixed until it became a uniform transparent solution to prepare a plasticizer solution.

(3) Production of interlayer film for laminated glass With respect to 100 parts by weight of the polyvinyl butyral resin,
40 parts by weight of the above-mentioned plasticizer solution, and an appropriate amount of magnesium 2-ethylbutyrate are added so that the magnesium content becomes 60 ppm with respect to the whole system, and this is sufficiently kneaded with a mixing roll, and then using a press molding machine. 30 at 150 ° C
Press molding was performed for a minute to obtain an intermediate film having an average film thickness of 0.76 mm.

(4) Manufacture of laminated glass The obtained interlayer film is 30 cm × 30 cm × from both ends thereof.
It is sandwiched by transparent float glass with a thickness of 2.5 mm, put in a rubber bag, and at a vacuum degree of 2660 Pa, 20
After degassing for a minute, transfer it to the oven with degassing for another 9
It vacuum-pressed, holding at 0 degreeC for 30 minutes. The thus preliminarily pressure-bonded laminated glass was pressure-bonded in an autoclave under the conditions of 135 ° C. and a pressure of 118 N / cm ² for 20 minutes to obtain a laminated glass.

(Example 2) Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester which is an ultraviolet absorber (manufactured by Clariant, Hostavin P
A laminated glass was produced in the same manner as in Example 1 except that the compounding amount of R-25) was 0.1 part by weight.

Example 3 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
PR-25) Instead of using 0.2 parts by weight, malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (Clariant, Hostavin P
R-25) 0.1 part by weight and 2- (2'-hydroxy-
3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole (manufactured by Ciba-Geigy, Tinuv)
in326) A laminated glass was produced in the same manner as in Example 1 except that 0.1 parts by weight of (in326) was also used.

(Example 4) Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
PR-25) Instead of using 0.2 parts by weight, malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (Clariant, Hostavin P
R-25) 0.05 part by weight and 2- (2'-hydroxy-3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole (manufactured by Ciba-Geigy, Tinu).
Vin 326) A laminated glass was produced in the same manner as in Example 1 except that 0.05 parts by weight of vin326) was used in combination.

Example 5 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
Instead of using 0.2 parts by weight of PR-25), 2-ethyl 2′-ethoxy-oxalanilide (Clariant) was used.
A laminated glass was produced in the same manner as in Example 1 except that 0.2 part by weight of Sanduvor VSU manufactured by Co., Ltd. was used.

(Example 6) Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
Instead of using 0.2 parts by weight of PR-25), 2-ethyl 2′-ethoxy-oxalanilide (Clariant) was used.
A laminated glass was produced in the same manner as in Example 1 except that 0.1 part by weight of Sanduvor VSU manufactured by the same company) was used.

Example 7 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
Instead of using 0.2 parts by weight of PR-25), 2-ethyl 2′-ethoxy-oxalanilide (Clariant) was used.
Manufactured by Sanduvor VSU) 0.1 part by weight and 2
Same as Example 1 except that 0.1 part by weight of-(2'-hydroxy-3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole (Tinuvin 326 manufactured by Ciba-Geigy) was used in combination. To produce a laminated glass.

Example 8 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
Instead of using 0.2 parts by weight of PR-25), 2-ethyl 2′-ethoxy-oxalanilide (Clariant) was used.
Made by Sanduvor VSU) 0.05 parts by weight,
2- (2'-hydroxy-3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole (Tibavin 326, manufactured by Ciba-Geigy Co., Ltd.) A laminated glass was produced in the same manner.

Comparative Example 1 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
Instead of using 0.2 parts by weight of PR-25), 2- (2 '
A laminated glass was prepared in the same manner as in Example 1 except that 0.2 part by weight of -hydroxy-3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole (Tinuvin 326, manufactured by Ciba-Geigy) was used. It was made.

Comparative Example 2 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber
Instead of using 0.2 parts by weight of PR-25), 2- (2 '
A laminated glass was prepared in the same manner as in Example 1 except that 0.1 part by weight of -hydroxy-3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole (Tinuvin 326, manufactured by Ciba-Geigy) was used. It was made.

(Comparative Example 3) Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
PR-25) Instead of using 0.2 part by weight, octabenzone (Chimassorb 81 manufactured by Ciba Geigy)
A laminated glass was produced in the same manner as in Example 1 except that 0.2 part by weight was used.

Comparative Example 4 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
PR-25) Instead of using 0.2 part by weight, octabenzone (Chimassorb 81 manufactured by Ciba Geigy)
A laminated glass was produced in the same manner as in Example 1 except that 0.1 part by weight was used.

Comparative Example 5 Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber
PR-25) Instead of using 0.2 parts by weight, 2,4-t
ert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate (manufactured by Ciba Geigy,
A laminated glass was produced in the same manner as in Example 1 except that 0.2 parts by weight of Tinuvin 120) was used.

(Comparative Example 6) Malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester (manufactured by Clariant, Hostavin as an ultraviolet absorber.
PR-25) Instead of using 0.2 parts by weight, 2,4-t
ert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate (manufactured by Ciba Geigy,
A laminated glass was produced in the same manner as in Example 1 except that 0.1 part by weight of Tinuvin 120) was used.

(Evaluation) The laminated glasses produced in Examples 1 to 8 and Comparative Examples 1 to 6 were evaluated by the following methods, and the results are shown in Table 1.

(1) Measurement of initial optical characteristics Using a direct writing spectrophotometer (U-4000 manufactured by Shimadzu Corporation), JIS Z 8722 and JIS R 310 are used.
According to 6, the visible light transmittance Tv (before SUV irradiation) in the wavelength range of 380 to 780 nm was determined.

(2) Super UV (SUV) irradiation test An irradiation sample of 5 cm x 10 cm was prepared under the following conditions:
Was irradiated with SUV. Test equipment: Eye Super UV Tester (manufactured by Iwasaki Electric Co.,
SUV-F11 type) UV intensity: 100 mW / cm² Limited wavelength: 295-450 nm Black panel temperature: 63 ℃ Irradiation time: 100, 200, 300 hours sampling Irradiation distance: 235mm

(3) Measurement of optical characteristics after SUV irradiation test After SUV irradiation, direct writing spectrophotometer (U-, manufactured by Shimadzu Corporation)
4000), JIS Z 8722 and JI
According to S R 3106, the visible light transmittance Tv (after SUV irradiation) in the wavelength range of 380 to 780 nm was measured, and Tv (before SUV irradiation) and Tv were calculated from the following formula (1).
The difference (ΔTv) from (after SUV irradiation) was determined. ΔTv = Tv (after SUV irradiation) -Tv (before SUV irradiation) (1)

[0061]

[Table 1]

From Table 1, in the laminated glasses produced in Examples 1 to 8, after the visible light transmittance was lowered by the SUV irradiation for the first 100 hours, the visible light transmission was continued even if the SUV was continuously irradiated. The rate did not decrease, so SUV
The visible light transmittance did not decrease significantly even after irradiation for 300 hours, and the durability was excellent. On the other hand, in the laminated glass produced in Comparative Examples 1 to 6, the longer the SUV irradiation time, the lower the visible light transmittance, and after 300 hours of SUV irradiation, the laminated glass produced in Examples 1 to 8 was less than that. The visible light transmittance was greatly reduced.

[0063]

According to the present invention, an interlayer film for laminated glass, which has excellent transparency and mechanical strength when formed into laminated glass, and which does not impair the initial optical quality even after a durability test, and
It is possible to provide a laminated glass using the interlayer film for laminated glass.

─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. ⁷ Identification code FI theme code (reference) C09J 7/00 C09J 7/00 129/14 129/14 C09K 3/00 104 C09K 3/00 104A 104B 104C 104D 104Z F Term (Reference) 4F071 AA29 AA30 AA80 AC10 AC12 AC19 AE04 AE05 AE20 AF13 AF30 AF57 AH03 BA01 BB03 BC01 4G061 FD19 FE06 EA036E036E036E036E036E036E036E036E0E036E0E036E036E0E036 FD079 FD310 FD342 FD348 GL00 GP00 4J004 AA08 AA11 AA17 AA18 BA02 FA08 FA10 4J040 DD071 HA146 HA156 HB19 HB30 HB32 HB37 HC01 HC12 HC25 JA09 KA10 KA29 KA31 LA06 LA10 MA05

Claims (5)

[Claims] 1. An interlayer film for laminated glass, which comprises a polyvinyl acetal resin, an ultraviolet absorber, a plasticizer, an adhesive strength modifier, and an antioxidant, wherein the ultraviolet absorber is a malonic acid ester-based compound and And / or an anilic acid anilide compound, an intermediate film for laminated glass. 2. The ultraviolet absorber is a group consisting of a malonic acid ester compound and / or an oxalic acid anilide compound, a benzotriazole compound, a benzophenone compound, a triazine compound, a benzoate compound, and a hindered amine compound. 2. A combination with at least one selected from the above.
The interlayer film for laminated glass described. 3. The adhesiveness adjusting agent is an alkali metal salt and / or
Or, it is an alkaline earth metal salt, and the ultraviolet absorber is 0.01 to 100 parts by weight with respect to the polyvinyl acetal resin.
5.0 parts by weight, 20 to 100 parts by weight of a plasticizer, 0.0001 to 1.0 parts by weight of the adhesive strength adjusting agent, and 0.01 to 5.0 parts by weight of an antioxidant are included. The interlayer film for laminated glass according to claim 1 or 2. 4. The polyvinyl acetal resin is a polyvinyl butyral resin.
Alternatively, the interlayer film for laminated glass according to item 3. 5. A laminated glass comprising the interlayer film for laminated glass according to claim 1, 2, 3 or 4.