JP6113643B2 - Laminate - Google Patents

Description

  The present invention relates to a laminate containing polyvinyl acetal.

  A sheet containing polyvinyl acetal and a plasticizer is widely used as an interlayer film for laminated glass because of its excellent adhesion and transparency to glass, mechanical strength and flexibility.

  When the moisture content of the interlayer film for laminated glass increases, the plasticizer may bleed (exudation), and when stored in a warehouse or the like, when the outside air temperature increases to 25 ° C to 40 ° C such as in summer. Under such a high temperature, the intermediate film is likely to be deformed or the interlayer films are likely to be blocked. Usually, it is stored in a warehouse, etc., adjusted to low temperature and low humidity so that plasticizer bleed, deformation and blocking do not occur by air conditioning equipment.

  However, when storing the interlayer film for laminated glass, the inside of the warehouse may become high temperature and high humidity due to, for example, a failure of the air conditioning equipment, and the moisture content of the interlayer film for laminated glass may become extremely high. If the interlayer film for laminated glass having a high water content is left as it is, water and plasticizer may be phase-separated in the interlayer film, or the plasticizer may bleed on the surface of the interlayer film. The transparency and mechanical properties of the interlayer film may deteriorate.

  By the way, in recent years, an interlayer film for multilayer laminated glass has been studied as an interlayer film for laminated glass having sound insulation properties. The interlayer film for sound insulating laminated glass includes a layer having a low plasticizer content for the purpose of expressing mechanical strength or exhibiting adhesiveness to glass, and a layer having a high plasticizer content for expressing sound insulating properties. In general, an interlayer film for sound-insulating multilayer laminated glass is used (see Patent Documents 1 and 2).

  When the interlayer film for multilayer laminated glass is also stored for a long time in a state of high moisture content, the moisture content becomes remarkably high, and water and plasticizer are phase-separated in the interlayer film, and the plasticizer bleeds on the surface of the interlayer film. Therefore, it is necessary to dry the interlayer film for multilayer laminated glass having a high moisture content in a low temperature and low humidity atmosphere. However, when an interlayer film for multilayer laminated glass having a high water content is rapidly dried in an atmosphere of low temperature and low humidity, the interlayer film becomes opaque due to phase separation of water and plasticizer from polyvinyl acetal in the interlayer film. In addition, water or a plasticizer may bleed between the interlayers of the intermediate film to cause delamination or decrease in transparency. In order to avoid these, there is a method of drying while gradually decreasing the temperature and humidity, but there is a problem that it takes a long time for drying.

  Further, the interlayer film for laminated glass generally contains a plasticizer, and the plasticizer is extracted by water adhering to the exposed portion of the interlayer film at the end of the laminated glass. May peel off or air bubbles may be generated to impair the appearance of the laminated glass. Depending on the type of plasticizer, the plasticizer may volatilize from the edge of the laminated glass when a laminated glass is produced through a decompression step or when used for a long time.

  By the way, when the interlayer film for laminated glass is used for a long period of time, there is a problem that the interlayer film deteriorates due to ultraviolet rays and yellows. In order to cope with this problem, an ultraviolet absorber is added for the purpose of improving the weather resistance of the interlayer film for laminated glass. However, as described above, when an ultraviolet absorber is added to a laminated interlayer film for laminated glass, the effect may not be sufficiently exhibited when used for a long period of time.

JP 2007-331959 A International Publication No. 2010/038801

  The present invention solves the above problems, and the plasticizer contained in the laminate is difficult to be extracted and volatilized by water, and a laminate having a high moisture content can be rapidly dried in an atmosphere of low temperature and low humidity. It is an object of the present invention to provide a laminate in which water and plasticizer are less likely to phase separate from polyvinyl acetal in the laminate and water or plasticizer is less likely to bleed between layers. Moreover, even if it is a case where it is a case where it uses for a long period of time as an intermediate film for laminated glasses, it aims at providing the laminated body which is hard to produce coloring and was excellent in durability.

According to the present invention, the above problem is that the A layer containing the polyvinyl acetal (A), the plasticizer (Ap), and the dispersant (Ad) whose average residual hydroxyl group amount is X (mol%), and the average residual hydroxyl group amount. Comprising a polyvinyl acetal (B) and a plasticizer (Bp) in which Y is mol%, and a B layer that may contain a dispersant (Bd), and X ≧ Y,
The layer A further contains a benzotriazole-based ultraviolet absorber, and the mass ratio of the content of the dispersant (Ad) to the content of the plasticizer (Ap) in the layer A is the plasticizer (Bp) in the layer B. Is larger than the mass ratio of the content of the dispersant (Bd) to the content of the plastic, and the plasticizer (Ap) is one molecule of m-valent alcohol (m represents a natural number of 2 to 4) and a monovalent carboxyl of 8 to 20 carbon atoms. An ester compound having a chemical structure obtained by an esterification reaction with an acid m molecule, the dispersant (Ad) having a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Ap); It is a compound having (m-1) to 1 hydroxyl group and 1 to (m-1) ester bonds, and the plasticizer (Bp) is one molecule of n-valent alcohol (n represents a natural number of 2 to 4). With n-molecule of monovalent carboxylic acid having 8 to 20 carbon atoms An ester compound having a chemical structure obtained by the conversion reaction, wherein the dispersant (Bd) has a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Bp), and (n-1) to This is solved by a laminate, which is a compound having one hydroxyl group and 1 to (n-1) ester bonds.

に示す構造を有する化合物、または、式（１）に示す構造を有し、式（１）中の任意の炭素原子に結合した水素原子の少なくとも一つが置換基により置換された化合物であることが好ましい。 A benzotriazole-based ultraviolet absorber has the formula (1):

Or a compound having the structure shown in formula (1) and having at least one hydrogen atom bonded to any carbon atom in formula (1) substituted by a substituent. preferable.

  It is preferable that at least one of the substituents is a hydrocarbon group having 4 to 8 carbon atoms.

  The benzotriazole ultraviolet absorber is preferably a compound having two or more substituents.

  The benzotriazole ultraviolet absorber is preferably a compound having a substituent at the ortho position of the hydroxyl group in the aromatic ring to which the hydroxyl group in Formula (1) is bonded.

  The molecular weight of the benzotriazole ultraviolet absorber is preferably 300 to 800.

  The m-valent alcohol is preferably a condensate of ethylene glycol having a degree of condensation of 3 to 20.

  The n-valent alcohol is preferably a condensate of ethylene glycol having a degree of condensation of 3 to 20.

  The average residual hydroxyl group amount X of the polyvinyl acetal (A) is preferably 20 to 40 mol%.

  The average residual hydroxyl group amount Y of the polyvinyl acetal (B) is preferably 10 to 35 mol%, and the average residual vinyl ester group amount is preferably 0.01 to 25 mol%.

  It is preferable that content of the plasticizer (Ap) with respect to 100 mass parts of polyvinyl acetal (A) in A layer is less than content of the plasticizer (Bp) with respect to 100 mass parts of polyvinyl acetal (B) in B layer.

  As for content of the plasticizer (Ap) in A layer, 20-60 mass parts is preferable with respect to 100 mass parts of polyvinyl acetal (A).

  As for content of the plasticizer (Bp) in B layer, 30-80 mass parts is preferable with respect to 100 mass parts of polyvinyl acetal (B).

  The monovalent carboxylic acid preferably has at least two organic groups other than a carbonyl group bonded to carbon adjacent to the carboxyl group.

  It is a laminate comprising three or more layers, and at least one of the two outer layers of the laminate is preferably an A layer.

  It is preferable that the laminate has a concavo-convex structure on at least one surface. Moreover, it is preferable that it is a laminated body whose 10-point average roughness Rz of the surface which has an uneven | corrugated structure is 30-70 micrometers.

  It is preferable that the moisture content of the laminate is 0.5% by mass or more and less than 0.65% by mass.

  According to the present invention, the above object is preferably achieved by providing a laminated glass including the laminate.

  According to the present invention, the plasticizer contained in the laminate is difficult to be extracted and volatilized by water, and even if the laminate having a high water content is rapidly dried in an atmosphere of low temperature and low humidity, It is possible to provide a laminate in which the plasticizer is less likely to phase separate from the polyvinyl acetal and is less likely to bleed between water and the plasticizer. Moreover, according to this invention, even if it is a case where it is a case where it is used over a long period of time as an intermediate film for laminated glasses, coloring cannot occur easily and the laminated body excellent in durability can be provided.

  The laminate of the present invention comprises an A layer containing polyvinyl acetal (A) having an average residual hydroxyl amount of X (mol%), a plasticizer (Ap) and a dispersant (Ad), and an average residual hydroxyl group amount of Y (mol). %)) And a plasticizer (Bp), and a B layer which may contain a dispersant (Bd).

  First, the polyvinyl acetal used in the present invention will be described.

  The average residual hydroxyl group amount X of the polyvinyl acetal (A) used in the present invention is not particularly limited, but is usually preferably 20 to 40 mol%, more preferably 23 to 38 mol%, still more preferably 25 to 36 mol%, 26 -29 mol% is particularly preferred. When the average residual hydroxyl group amount X is less than 20 mol%, the mechanical strength of the resulting laminate and the adhesion to glass may be reduced. When it exceeds 40 mol%, it is in phase with the plasticizer (Ap). Solubility may be significantly reduced.

  The average degree of acetalization of the polyvinyl acetal (A) is not limited, but is usually preferably 50 to 78 mol%, more preferably 60 to 74 mol%, and further preferably 65 to 73 mol%. If the average degree of acetalization is less than 50 mol%, the compatibility with the plasticizer (Ap) may be significantly reduced, and if it exceeds 78 mol%, the mechanical strength of the resulting laminate may be reduced. is there.

  The average residual vinyl ester group amount of the polyvinyl acetal (A) is not particularly limited, but is usually preferably 0.01 to 15 mol%, more preferably 0.01 to 10 mol%, and still more preferably 0.01 to 5 mol%. . When the average residual vinyl ester group amount is less than 0.01 mol%, it is difficult to produce industrially inexpensively. When the average vinyl ester group amount exceeds 15 mol%, when the resulting laminate is used for a long period of time, vinyl ester groups are not formed. The laminated body is likely to be colored due to hydrolysis.

  The average residual hydroxyl group amount Y of the polyvinyl acetal (B) used in the present invention is not particularly limited, but is usually preferably 10 to 35 mol%, more preferably 13 to 33 mol%, further preferably 15 to 30 mol%. If the average residual hydroxyl group amount Y is less than 10 mol%, the mechanical strength and the adhesion to glass may be significantly reduced, and if it exceeds 35 mol%, the compatibility with the plasticizer (Bp) may be reduced. is there.

  The average degree of acetalization of the polyvinyl acetal (B) is not limited, but is usually preferably 60 to 84 mol%, more preferably 65 to 82 mol%, and further preferably 70 to 80 mol%. If the average degree of acetalization is less than 60 mol%, the compatibility with the plasticizer (Bp) may be lowered, and if it exceeds 84 mol%, the mechanical strength of the resulting laminate may be lowered.

  The average residual vinyl ester group amount of the polyvinyl acetal (B) is not particularly limited, but is usually preferably 0.01 to 25 mol%, more preferably 3 to 16 mol%, still more preferably 3 to 15 mol%, and 4 to 13 Mole% is particularly preferred. Those having an average residual vinyl ester group amount of less than 0.01 mol% are difficult to produce industrially at low cost, and the compatibility with the plasticizer (Bp) may be lowered. On the other hand, when the content exceeds 25 mol%, the laminate is likely to be colored due to hydrolysis of the vinyl ester group when the resulting laminate is used for a long period of time.

  The average residual hydroxyl group amount X of the polyvinyl acetal (A) is equal to or larger than the average residual hydroxyl group amount Y of the polyvinyl acetal (B), more preferably 3 to 20 mol%, more preferably 5 to 15 mol%. A large size is particularly preferred. When satisfying the relationship of the average residual hydroxyl group content, water and plasticizers are difficult to phase separate from polyvinyl acetal in the laminate even if the laminate having a high water content is rapidly dried in an atmosphere of low temperature and low humidity. Further, it is preferable that bleeding between layers of water or a plasticizer does not easily occur, and it is preferable from the viewpoint of sound insulation performance when the laminate is used as an interlayer film for sound insulation laminated glass.

  The polyvinyl acetal (A) and the polyvinyl acetal (B) used in the present invention are produced using polyvinyl alcohol as a raw material. Polyvinyl alcohol can be obtained by a known method. That is, it can be obtained by polymerizing a vinyl ester compound and saponifying the obtained polymer. As a method for polymerizing the vinyl ester compound, known methods such as a solution polymerization method, a bulk polymerization method, a suspension polymerization method, and an emulsion polymerization method can be applied. As a polymerization initiator used in these polymerization methods, an azo initiator, a peroxide initiator, a redox initiator, or the like can be used as appropriate. The saponification reaction is carried out by subjecting the vinyl ester group of the polymer to alcoholysis or hydrolysis using a known alkali catalyst or acid catalyst. Among them, the saponification reaction using methanol as a solvent and caustic soda (NaOH) as a catalyst is simple and most preferable.

  Examples of the vinyl ester compound include known carboxylic acid vinyl esters such as vinyl formate, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl stearate, vinyl benzoate, and vinyl acetate is preferred.

  Also, unless the polyvinyl alcohol is contrary to the gist of the present invention, a modified polyvinyl alcohol obtained by saponifying a copolymer obtained by copolymerizing a vinyl ester compound and a monomer copolymerizable with the vinyl ester compound is used. You can also The monomer copolymerizable with the vinyl ester compound is usually used in a proportion of less than 10 mol% with respect to the vinyl ester compound.

  The viscosity average polymerization degree of polyvinyl alcohol used as a raw material for the polyvinyl acetal used in the present invention is not particularly limited and can be appropriately selected according to the use, but is preferably 150 to 3000, more preferably 200 to 2500, and 1000 to 2000. Is more preferable. When the viscosity average degree of polymerization of polyvinyl alcohol is lower than 150, the mechanical strength of the obtained laminate tends to be insufficient, and when it is higher than 3000, the handleability of the obtained laminate may be deteriorated.

  The polyvinyl acetal used in the present invention can be produced by a known method. For example, it can be produced by a precipitation method under the following reaction conditions. First, a polyvinyl alcohol aqueous solution having a concentration of 3 to 40% by mass is maintained in a temperature range of 80 to 100 ° C. and then gradually cooled over 10 to 60 minutes. When the temperature is lowered to −10 to 30 ° C., an aldehyde and an acid catalyst are added, and an acetalization reaction is performed for 30 to 300 minutes while keeping the temperature constant. At that time, polyvinyl acetal having a certain degree of acetalization is deposited. Thereafter, the reaction solution is heated to a temperature of 30 to 80 ° C. over 30 to 300 minutes, and the temperature is maintained for 10 to 500 minutes. Next, by adding a basic compound to the reaction solution, the acid catalyst is neutralized, washed with water, and dried to obtain polyvinyl acetal.

  The acid catalyst used in the acetalization reaction is not particularly limited, and any of organic acids such as acetic acid and paratoluenesulfonic acid or inorganic acids such as nitric acid, sulfuric acid and hydrochloric acid can be used, and hydrochloric acid, sulfuric acid and nitric acid are particularly preferable. .

  Although the aldehyde used for acetalization reaction is not specifically limited, It is preferable to acetalize with a C1-C8 aldehyde. Among them, it is preferable to use an aldehyde having 4 to 6 carbon atoms, and it is particularly preferable to use n-butyraldehyde. In the present invention, polyvinyl acetal obtained by using two or more aldehydes in combination can also be used.

  The plasticizer (Ap) contained in the layer A constituting the laminate of the present invention has a chemical structure obtained by an esterification reaction between one molecule of m-valent alcohol and m molecule of monovalent carboxylic acid having 8 to 20 carbon atoms. It is an ester compound. Here, m represents a natural number of 2 to 4. However, the plasticizer (Ap) only needs to have a chemical structure obtained by an esterification reaction between one molecule of m-valent alcohol and one molecule of monovalent carboxylic acid having 8 to 20 carbon atoms. You may use what was obtained by methods other than esterifying a C8-C20 monovalent carboxylic acid m molecule.

  Examples of m-valent alcohols include dihydric alcohols such as ethylene glycol, ethylene glycol condensate, propylene glycol, propylene glycol condensate, 3-methyl-1,5-pentanediol, 1,4-cyclohexanedimethanol; glycerin And trihydric alcohols such as erythritol and pentaerythritol. Among them, the obtained plasticizer (Ap) is excellent in compatibility with the polyvinyl acetal (A) and plasticizing effect, has a high boiling point, and is bivalent from the viewpoint that even when the laminate is in contact with water, it is difficult to extract with water. Alcohols are preferred, ethylene glycol condensates such as triethylene glycol and tetraethylene glycol are more preferred, ethylene glycol having a degree of condensation of 3 to 20 is more preferred, and ethylene glycol condensates having a degree of condensation of 3 to 10 are preferred. Particularly preferred is a condensate of ethylene glycol having a degree of condensation of 3 or 4.

  Examples of the monovalent carboxylic acid having 8 to 20 carbon atoms include octanoic acid, 2-ethylhexanoic acid, nonanoic acid, decanoic acid, dodecanoic acid, hexadecanoic acid, 2-methylheptanoic acid, 2-ethylheptanoic acid, 2,2 -Dimethylhexanoic acid, palmitic acid, stearic acid, oleic acid, linoleic acid and the like. Among these, monovalent carboxylic acids having 8 to 12 carbon atoms, particularly 8 to 10 carbon atoms, are excellent in compatibility with the polyvinyl acetal (A) of the obtained plasticizer (Ap) and plasticizing effect, and have a high boiling point. Further, even when the laminate is in contact with water, it is preferable from the viewpoint of being hardly extracted with water. Moreover, the monovalent carboxylic acid in which at least two organic groups other than the carboxyl group are bonded to the carbon adjacent to the carboxyl group is preferable from the viewpoint of enhancing the hydrolysis resistance of the plasticizer (Ap). Examples of such monovalent carboxylic acids include 2-ethylhexanoic acid, 2-methylheptanoic acid, 2-ethylheptanoic acid, and 2,2-dimethylhexanoic acid.

  Examples of ester compounds having a chemical structure obtained by esterification reaction of 1 molecule of m-valent alcohol and m-molecule of monovalent carboxylic acid having 8 to 20 carbon atoms include, for example, triethylene glycol di-2-ethylhexanoate, tetraethylene glycol Di-2-ethylhexanoate, triethylene glycol dinonanoate, triethylene glycol didecanoate, triethylene glycol didodecanoate, decaethylene glycol di-2-ethylhexanoate, glycerin tri-2-ethylhexanoate, etc. Is mentioned. Among them, triethylene glycol di-2-ethylhexanoate, tetraethylene glycol di-2-ethylhexanoate, triethylene glycol dinonanoate, and glycerin tri-2-ethylhexanoate are compatible with polyvinyl acetal (A). And it is excellent from the viewpoint that it is excellent in plasticizing effect, has a high boiling point, and is difficult to be extracted with water even when the laminate is in contact with water. These may be used alone or in combination of two or more.

  Although content of the plasticizer (Ap) in A layer which comprises the laminated body of this invention is not specifically limited, Usually 20-60 mass parts is preferable with respect to 100 mass parts of polyvinyl acetal (A), 25-55 mass parts. Is more preferable, and 30-50 mass parts is further more preferable. When the content of the plasticizer (Ap) is less than 20 parts by mass with respect to 100 parts by mass of the polyvinyl acetal (A), the resulting laminate tends to have insufficient flexibility and impact as an interlayer film for laminated glass. Absorption may be a problem. On the other hand, when the amount is more than 60 parts by mass, the mechanical strength of the obtained laminate tends to be insufficient.

  The plasticizer (Bp) contained in the B layer constituting the laminate of the present invention has a chemical structure obtained by an esterification reaction of one molecule of n-valent alcohol and n molecule of monovalent carboxylic acid having 8 to 20 carbon atoms. It is an ester compound. Here, n represents a natural number of 2-4. However, the plasticizer (Bp) only needs to have a chemical structure obtained by esterification reaction between one molecule of n-valent alcohol and one molecule of monovalent carboxylic acid having 8 to 20 carbon atoms. You may use what was obtained by methods other than esterifying a C8-C20 monovalent carboxylic acid n molecule.

  Examples of the n-valent alcohol include the same compounds as those exemplified as the m-valent alcohol, and preferred compounds are also the same.

  Examples of ester compounds having a chemical structure obtained by esterification reaction of one molecule of n-valent alcohol and one molecule of monovalent carboxylic acid having 8 to 20 carbon atoms include triethylene glycol di-2-ethylhexanoate and tetraethylene glycol. Di-2-ethylhexanoate, triethylene glycol dinonanoate, triethylene glycol didecanoate, triethylene glycol didodecanoate, decaethylene glycol di-2-ethylhexanoate, glycerin tri-2-ethylhexanoate, etc. Is mentioned. Among them, triethylene glycol di-2-ethylhexanoate, tetraethylene glycol di-2-ethylhexanoate, triethylene glycol dinonanoate, and glycerin tri-2-ethylhexanoate are compatible with polyvinyl acetal (B). And it is excellent from the viewpoint that it is excellent in plasticizing effect, has a high boiling point, and is difficult to be extracted with water even when the laminate is in contact with water. These may be used alone or in combination of two or more.

  Although content of the plasticizer (Bp) in B layer which comprises the laminated body of this invention is not specifically limited, Usually 30-80 mass parts is preferable with respect to 100 mass parts of polyvinyl acetal (B), 33-75 mass parts. Is more preferable, and 40-70 mass parts is further more preferable. When the content of the plasticizer (Bp) is less than 30 parts by mass with respect to 100 parts by mass of the polyvinyl acetal (B), a desired sound insulation is exhibited when the obtained laminate is used for an interlayer film for sound insulation laminated glass. There are cases where it is not possible. On the other hand, when the amount is more than 80 parts by mass, the resulting laminated body tends to have insufficient mechanical strength.

  In the present invention, the relationship between the content of the plasticizer (Ap) in the A layer and the content of the plasticizer (Bp) in the B layer is not strictly limited, but the polyvinyl acetal (A) 100 in the A layer is not limited. It is preferable that content of the plasticizer (Ap) with respect to a mass part is less than content of the plasticizer (Bp) with respect to 100 mass parts of polyvinyl acetal (B) in B layer. From the standpoint that sound insulation can be exhibited in the laminated glass using the laminate of the present invention, the plasticizer (Ap) content relative to 100 parts by mass of the polyvinyl acetal (A) is a plasticizer relative to 100 parts by mass of the polyvinyl acetal (B) ( The content of Bp) is preferably 5 to 60 parts by mass and more preferably 10 to 40 parts by mass.

  Next, the dispersant (Ad) will be described. The dispersant (Ad) has a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Ap), and (m-1) to 1 hydroxyl group and 1 to (m-1). It is a compound having an ester bond. However, the dispersant (Ad) may have a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Ap), and may be obtained by a method other than hydrolyzing the plasticizer (Ap). You may use what was made. Examples of the dispersant (Ad) include triethylene glycol mono-2-ethylhexanoate (chemical structure obtained by hydrolyzing one ester bond of triethylene glycol di-2-ethylhexanoate), tetraethylene glycol mono-2-ethyl, and the like. Hexanoate (chemical structure hydrolyzing one ester bond of tetraethylene glycol di-2-ethylhexanoate), triethylene glycol monodecanoate (hydrolyzing one ester bond of triethylene glycol didecanoate) Chemical structure), triethylene glycol monododecanoate (chemical structure obtained by hydrolyzing one ester bond of tetraethylene glycol didodecanoate), decaethylene glycol mono-2-ethylhexanoate (decaethylene glycol di-2-ethylhexanoate) Chemical structure hydrolyzed one ester bond of noate), triethylene glycol monononanoate (chemical structure hydrolyzed one ester bond of triethylene glycol dinonanoate), glycerin di-2-ethylhexanoate (glycerin) Chemical structure obtained by hydrolyzing one ester bond of tri-2-ethylhexanoate), glycerin mono 2-ethylhexanoate (chemical structure obtained by hydrolyzing two ester bonds of glycerin tri-2-ethylhexanoate), etc. Is mentioned. Among them, triethylene glycol mono 2-ethylhexanoate, tetraethylene glycol mono 2-ethyl hexanoate, and triethylene glycol monononanoate are liquid at room temperature and excellent in handleability, and polyvinyl acetal (A) and plasticizer It is suitable because it is particularly excellent in compatibility with (Ap).

  Although content of the dispersing agent (Ad) in A layer which comprises the laminated body of this invention is not specifically limited, 0.01-6 mass parts is preferable normally with respect to 100 mass parts of polyvinyl acetal (A), and 0.06. -4 parts by mass is more preferable, and 0.09-2.4 parts by mass is more preferable. When the content of the dispersant (Ad) is less than 0.01 parts by mass, when a laminate having a high water content is rapidly dried in an atmosphere of low temperature and low humidity, water or a plasticizer is contained in the polyvinyl acetal. Phase separation may cause the laminate to become opaque, or water or a plasticizer may bleed between the layers of the laminate to cause delamination or a decrease in transparency. On the other hand, when the amount exceeds 6 parts by mass, when the dispersant (Ad) volatilizes or the A layer comes into contact with water, the dispersant (Ad) is extracted with water, and the physical properties of the A layer may change. .

  The dispersant (Bd) has a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Bp), and (n-1) to 1 hydroxyl group and 1 to (n-1). It is a compound having an ester bond. However, the dispersant (Bd) may have a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Bp), and may be obtained by a method other than hydrolyzing the plasticizer (Bp). You may use what was made. Examples of the dispersant (Bd) include triethylene glycol mono-2-ethylhexanoate, tetraethylene glycol mono-2-ethylhexanoate, triethylene glycol monodecanoate, triethylene glycol monododecanoate, and decaethylene glycol. Examples include mono-2-ethylhexanoate, triethylene glycol monononanoate, glycerin di-2-ethylhexanoate, and glycerin mono-2-ethylhexanoate. Among them, triethylene glycol mono 2-ethylhexanoate, tetraethylene glycol mono 2-ethyl hexanoate, and triethylene glycol monononanoate are liquid at room temperature and excellent in handleability, and polyvinyl acetal (B) and plastic This is preferred because it is particularly excellent in compatibility with the agent (Bp).

  Although content of the dispersing agent (Bd) in B layer which comprises the laminated body of this invention is not specifically limited, 0-4 mass parts is preferable normally with respect to 100 mass parts of polyvinyl acetal (B), and 0.01-3. A mass part is more preferable, and 0.03-2.2 mass parts is further more preferable. In addition, that content of a dispersing agent (Bd) is 0 mass part means that a dispersing agent (Bd) is not included in B layer. When the content of the dispersing agent (Bd) exceeds 4 parts by mass, the dispersing agent (Bd) volatilizes or when the B layer comes into contact with water, the dispersing agent (Bd) is extracted with water. Physical properties may change.

In the present invention, the mass ratio of the content of the plasticizer in the layer A dispersing agent to the content of (Ap) (Ad) (hereinafter, referred to as mass ratio W _A) is, B layer of the plasticizer (Bp) the mass ratio of the content of the dispersing agent with respect to the content (Bd) (hereinafter, referred to as mass ratio W _B) is required to be greater than. Preferably the weight ratio _{W B} is 0, or the mass ratio _{W A} is not less than 1.05 times the mass ratio B. More preferably the weight ratio _{W A} mass ratio _{W B} of 1.1 times or more, more preferably 1.25 times or more, particularly preferably 1.5 times or more. Stack weight ratio W _A is equal to or less than the mass ratio W _B is water or a plasticizer in the laminate in the case obtained by rapidly drying in an atmosphere of low temperature and low humidity high stack water content polyvinyl acetal and Phase It may become separated and become opaque, or water or a plasticizer may bleed between the layers of the laminate, causing delamination or a decrease in transparency.

  In the present invention, the plasticizer (Ap) and the plasticizer (Bp) may be the same or different, but are preferably the same from the viewpoint of reducing costs in the production of the A layer and the B layer.

  The laminate of the present invention further contains a benzotriazole-based ultraviolet absorber in the A layer. By including a benzotriazole-based ultraviolet absorber in the A layer, coloring of the laminate can be suppressed and durability can be improved. When an ultraviolet absorber other than the benzotriazole ultraviolet absorber is used, the durability of the A layer is impaired when the laminate is used as an interlayer film for laminated glass over a long period of time. On the other hand, when a benzotriazole-based ultraviolet absorber is used, the ultraviolet absorber is stably held in the A layer, and the durability of the laminate can be improved.

に示す構造を有する化合物、または、式（１）に示す構造を有し、式（１）中の任意の炭素原子に結合した水素原子の少なくとも一つが置換基により置換された化合物であることが好ましい。紫外線吸収剤が、このような化合物である場合、結果として積層体の着色、特に合わせガラスの端部での着色を抑制することができる。 In the present invention, the benzotriazole-based ultraviolet absorber can be used without particular limitation as long as it is a compound containing a benzotriazole structure, but the formula (1):

Or a compound having the structure shown in formula (1) and having at least one hydrogen atom bonded to any carbon atom in formula (1) substituted by a substituent. preferable. When an ultraviolet absorber is such a compound, as a result, the coloring of a laminated body, especially the coloring in the edge part of a laminated glass can be suppressed.

  When the compound having the structure represented by the formula (1) has a substituent, a compound having two or more substituents is preferable from the viewpoint of suppressing coloration of the laminate. Moreover, when there are two or more substituents, they may be the same or different.

  Although it does not specifically limit as said substituent, It is preferable that it is what does not change the polarity of the compound which has a structure shown in Formula (1) remarkably, Specifically, for example, a methyl group, an ethyl group, a propyl group, n -Linear or branched hydrocarbon groups such as butyl group, t-butyl group and octyl group; halogen atoms such as chlorine atom and bromine atom. Among these substituents, even when the laminate is used for a long period of time, it is excellent in the effect of suppressing the coloration of the laminate, is excellent in compatibility with polyvinyl acetal, and suppresses movement between the layers. A hydrogen group is preferable, and a hydrocarbon group having 4 to 8 carbon atoms is more preferable. When the number of substituents is 2 or more, at least one is preferably a hydrocarbon group, and more preferably a hydrocarbon group having 4 to 8 carbon atoms.

  As described above, the substituent is not particularly limited as long as a hydrogen atom bonded to an arbitrary carbon atom in the formula (1) is substituted. However, from the viewpoint of excellent effect of suppressing coloration of the laminate, the formula (1) In the aromatic ring to which the hydroxyl group of the compound having the structure shown below is bonded, a compound having a substituent at the ortho position of the hydroxyl group is preferable. The substituent at the ortho position is preferably a hydrocarbon group, more preferably a hydrocarbon group having 4 to 8 carbon atoms.

  Further, the molecular weight of the benzotriazole-based ultraviolet absorber is not particularly limited, but is preferably 300 to 800, more preferably 300 to 600, still more preferably 300 to 500, It is especially preferable that it is 300-400. When the molecular weight of the benzotriazole-based ultraviolet absorber is smaller than 300, discoloration of the end of the laminate tends to occur, and when used for a long period, it tends to be colored. On the other hand, when the molecular weight of the benzotriazole-based ultraviolet absorber is larger than 800, the compatibility with polyvinyl acetal is lowered, and the transparency of the obtained laminate may be lowered.

  Specific examples of the benzotriazole-based ultraviolet absorber include, for example, formulas (2) to (5), but are not limited thereto, and other than the optional substituents and hydrogen atoms exemplified above Also included within the scope of the present invention.

  In the laminate of the present invention, the benzotriazole-based ultraviolet absorbers may be used alone or in combination of two or more. Although content of a benzotriazole type ultraviolet absorber is not specifically limited, 0.0001-5 mass% is preferable normally with respect to the total mass of A layer of a laminated body, and 0.001-1 mass% is more preferable. If the content of the benzotriazole-based UV absorber is less than 0.0001% by mass, a sufficient effect as the UV absorber may not be obtained, and the content of the benzotriazole-based UV absorber may exceed 5% by mass. Even if you increase it, you can not expect much effect.

  Further, ultraviolet absorbers other than benzotriazoles such as oxalic anilide ultraviolet absorbers and benzoate ultraviolet absorbers can be used in combination as long as the effects of the present invention are not impaired.

  The laminate of the present invention may further contain an antioxidant, an adhesion improver, and other additives.

  There is no limitation in particular in the kind of antioxidant which the laminated body of this invention may contain. For example, a well-known phenolic antioxidant, phosphorus antioxidant, sulfur antioxidant, etc. can be used. Of these, phenolic antioxidants are preferred. Antioxidants may be used alone or in combination of two or more. When it contains antioxidant, the quantity is not specifically limited, However 0.0001-5 mass% is preferable normally with respect to the mass of a laminated body, and 0.001-1 mass% is more preferable. When the amount is less than 0.0001% by mass, a sufficient effect as an antioxidant may not be obtained, and when the amount is more than 5% by mass, a remarkable effect cannot be expected.

  The laminate of the present invention is particularly preferably used as an interlayer film for laminated glass. In that case, it is preferable that an adhesion adjusting agent is added to the layer that adheres to the glass. Examples of the adhesion adjusting agent include sodium salt, potassium salt, magnesium salt and the like of organic acids such as acetic acid, propionic acid, butanoic acid, hexanoic acid, 2-ethylbutanoic acid and 2-ethylhexanoic acid. More than one kind may be added.

  In particular, when the layer that adheres to the glass is the A layer, a magnesium salt such as magnesium acetate, magnesium acetate tetrahydrate, magnesium butanoate, magnesium 2-ethylbutanoate, magnesium 2-ethylhexanoate is added to the A layer. It is preferable. The addition amount of the adhesion adjusting agent is 0.001 to 0.1 parts by mass with respect to 100 parts by mass of the polyvinyl acetal (A) from the viewpoint of penetration resistance of the laminated glass and prevention of glass fragment scattering when the laminated glass is broken. Is preferable, 0.005-0.08 mass part is more preferable, 0.01-0.06 mass part is further more preferable, 0.03-0.055 mass part is especially preferable. Magnesium salt absorbs less water than potassium salt and sodium salt, so when magnesium salt is added to layer A as an adhesive strength modifier, a laminate with a high moisture content is rapidly applied in a low temperature and low humidity atmosphere. Even when dried, water and plasticizer are difficult to phase separate from polyvinyl acetal in the laminate, and water and plasticizer are difficult to bleed between layers of the laminate.

  The method for producing the laminate of the present invention is not particularly limited, and conventionally known methods can be applied. For example, after the components constituting the A layer and the components constituting the B layer are melt-kneaded with an extruder and then co-extruded with a multilayer film forming machine; the A layer individually prepared by hot pressing or casting after the melt-kneading And a method of laminating and laminating the B layers and adhering them by hot pressing or the like, if necessary.

  The moisture content of the laminate of the present invention is not particularly limited, but if the moisture content is too high, the plasticizer may bleed from the laminate. -0.8 mass% is more preferable, and 0.2-0.7 mass% is further more preferable. Further, from the viewpoint of appropriately adjusting the adhesion of the laminate of the present invention to glass, the water content is preferably 0.5% by mass or more and less than 0.65% by mass, and more preferably 0.5% by mass or more. More preferably, it is less than 0.6% by mass. When the moisture content is less than 0.5% by mass, the adhesiveness between the laminate of the present invention and the glass may be too high, and when the moisture content exceeds 0.65% by mass, the present moisture content is increased. When the laminate of the present invention is stored for a long time, the laminate of the present invention may be easily colored by ultraviolet rays or the like, and the adhesion to glass may be lowered.

  There is no limitation in particular in the thickness of A layer and B layer in the laminated body of this invention. The thickness of the A layer is usually preferably 0.05 to 1.2 mm, more preferably 0.07 to 1 mm, and further preferably 0.1 to 0.7 mm. If it is thinner than 0.05 mm, the mechanical strength of the laminate of the present invention tends to decrease, and if it is thicker than 1.2 mm, the flexibility of the laminate of the present invention tends to be insufficient, as an interlayer film for laminated glass. In use, the safety of the resulting laminated glass may be reduced.

  The thickness of the B layer is usually preferably 0.01 to 1 mm, more preferably 0.02 to 0.8 mm, and even more preferably 0.05 to 0.5 mm. If it is thinner than 0.01 mm, the sound insulation performance of the laminated glass having the laminate of the present invention as an intermediate film may be deteriorated, and even if it is thicker than 1 mm, the mechanical strength of the laminate of the present invention does not tend to improve any more. It is in.

  Further, the ratio of the thickness of the A layer and the thickness of the B layer is not particularly limited, but is preferably 0.05 to 4, more preferably 0.07 to 2, more preferably 0.1 to 2, from the viewpoint of the mechanical strength and the sound insulation. 0.8 is more preferable.

  In the laminate of the present invention, at least one of the outermost layers of the laminate is preferably an A layer. Examples of such laminates are A layer / B layer / A layer, A layer / B layer / A layer / B layer / A layer and the like. A laminate in which one of the outermost layers such as A layer / B layer / A layer / B layer is the A layer can be mentioned. In particular, when the laminate of the present invention is used as an interlayer film for laminated glass, it is preferable that both outermost layers are A layers because the adhesiveness between the laminate and the glass can be adjusted appropriately.

  When the laminate of the present invention is used as an interlayer film for laminated glass, the thickness of the laminate is not particularly limited, but usually 0.2 to 2 mm is preferable, 0.25 to 1.8 mm is more preferable, and 3-1.5 mm is more preferable. When the thickness of the laminate is thinner than 0.2 mm, the mechanical strength tends to be insufficient, and when it is thicker than 2 mm, the flexibility tends to be insufficient.

  The glass material when using the laminate of the present invention as an interlayer film for laminated glass is not particularly limited, inorganic glass such as float plate glass, heat tempered glass, chemically tempered glass; organic glass such as polymethyl methacrylate, polycarbonate, etc. Conventionally known glass can be used. These may be colorless or colored, transparent or non-transparent, and two or more of them may be used in combination. Although there is no limitation in particular in the thickness of glass, Usually, 20 mm or less is preferable and 10 mm or less is more preferable.

  When using the laminated body of the present invention as an interlayer film for laminated glass, the shape of the outermost surface of the laminated body is not particularly limited, but considering the handleability when producing a laminated glass (for example, bubble removal in the laminate), It is preferable to form a concavo-convex structure on at least one surface of the laminate by a known method such as melt fracture or embossing. In the case of forming a concavo-convex structure, the shape is not particularly limited. However, when the ten-point average roughness Rz (measured according to JIS B0031-1994) is used as an index, the shape is preferably 30 to 70 μm, and 30 to 60 μm. It is more preferable that When the ten-point average roughness Rz is less than 30 μm, deaeration may be insufficient when a laminated glass is produced using the laminate of the present invention as an interlayer film for laminated glass, and handling properties at the time of producing laminated glass May decrease. On the other hand, when the thickness exceeds 70 μm, it may take a long time to make the concavo-convex structure disappear when producing laminated glass, and the surface area of the laminate may be increased. Therefore, depending on the method for producing a laminated glass that undergoes a decompression step, such as a method using a vacuum bag, moisture and components contained in the laminate of the present invention are likely to volatilize, and the laminate of the present invention contained in the laminated glass. It may be difficult to adjust the water content and the amount of each main component.

  The method of producing laminated glass using the laminate of the present invention as an interlayer film for laminated glass is not particularly limited. For example, a method of undergoing a pressure reducing process using a vacuum laminator device or a vacuum bag; Known methods such as a processing method can be mentioned.

An example of the production conditions when using a vacuum laminator apparatus is as follows: glass at a temperature of 100 to 200 ° C., preferably 130 to 160 ° C. under a reduced pressure of 1 × 10 ^{−6 to} 3 × 10 ⁻² MPa. An interlayer film for laminated glass is laminated. A method using a vacuum bag is described, for example, in EP 1356683. For example, lamination is performed at 130 to 145 ° C. under a pressure of about 2 × 10 ⁻² MPa.

  In the method of processing by an autoclave after temporarily bonding with a nip roll, an example of the operating condition of the nip roll is that the glass and the laminate are heated to 30 to 70 ° C. with an infrared heater or the like, and then deaerated by being sandwiched between rolls and further 50 to 50- After heating to 120 ° C., the film is temporarily bonded by pressing with a roll. The process of processing by an autoclave is implemented for 30 minutes-200 minutes at the temperature of 130-145 degreeC under the pressure of 1.0-1.5 MPa, for example.

  EXAMPLES Hereinafter, although an Example etc. demonstrate this invention further in detail, this invention is not limited at all by these Examples.

(Preparation of PVB-1)
In a 3 L (liter) glass container equipped with a reflux condenser, thermometer, and squid type stirring blade, ion exchange water 2000 g, polyvinyl alcohol (PVA-1) (viscosity average polymerization degree 1700, saponification degree 99 mol%) 200 g (PVA concentration 9.1%), and the contents were heated to 95 ° C. and completely dissolved. Next, the mixture was gradually cooled to 7 ° C. over about 30 minutes with stirring at 120 rpm, 113 g of butyraldehyde and 70 g of 35% hydrochloric acid were added, and a butyralization reaction was performed for 30 minutes. Thereafter, the temperature was raised to 60 ° C. over 60 minutes, held at 60 ° C. for 120 minutes, and then immediately cooled in a cold water bath. After washing the polyvinyl acetal resin with ion-exchanged water, the remaining acid catalyst was neutralized with an aqueous sodium hydroxide solution, further washed with ion-exchanged water, dehydrated and dried to obtain polyvinyl butyral (PVB-1). . When the obtained PVB-1 was measured according to JIS K6728-1977 (hereinafter referred to as JIS K6728), as shown in Table 1, the average degree of acetalization was 68 mol%, and the average residual vinyl ester group amount was 1 mol%. The average residual hydroxyl group amount was 31 mol%.

(Preparation of PVB-2)
In the preparation of PVB-1, the reaction was carried out in the same manner except that the amount of butyraldehyde used was changed to 118 g to obtain PVB-2. The obtained PVB-2 was measured according to JIS K6728. As shown in Table 1, the average degree of acetalization was 71 mol%, the average residual vinyl ester group amount was 1 mol%, and the average residual hydroxyl group amount was 28 mol%. there were.

(Preparation of PVB-3)
In the preparation of PVB-1, PVA-1 was changed to 200 g of PVA-2 (viscosity average polymerization degree 1700, saponification degree 92 mol%), but butyraldehyde was used in an amount of 122 g, and a butyralization reaction was carried out at 5 ° C. After the implementation, the temperature was raised to 68 ° C. over 70 minutes, and PVB-3 was obtained in the same manner except that the reaction was performed at 68 ° C. for 100 minutes. The obtained PVB-3 was measured according to JIS K6728. As shown in Table 1, the average degree of acetalization was 74 mol%, the average residual vinyl ester group amount was 6 mol%, and the average residual hydroxyl group amount was 20 mol%. there were.

(Preparation of PVB-4)
In the preparation of PVB-3, PVA-2 was changed to 200 g of PVA-3 (viscosity average polymerization degree 1700, saponification degree 89 mol%), but butyraldehyde was used in an amount of 117 g, and a butyralization reaction was carried out at 5 ° C. After the implementation, the temperature was raised to 65 ° C. over 70 minutes, and PVB-4 was obtained in the same manner except that the reaction was performed at 65 ° C. for 140 minutes. The obtained PVB-4 was measured according to JIS K6728. As shown in Table 1, the average degree of acetalization was 75 mol%, the average residual vinyl ester group amount was 9 mol%, and the average residual hydroxyl group amount was 16 mol%. there were.

Example 1
(Production of laminate)
100 parts by mass of PVB-1, 39 parts by mass of triethylene glycol di-2-ethylhexanoate as a plasticizer (Ap), 0.3 parts by mass of triethylene glycol mono-2-ethylhexanoate as a dispersant (Ad) Eight and 0.1 parts by mass of an ultraviolet absorber (UVA-1) were kneaded in a lab plast mill at 160 ° C. for 8 minutes. The obtained kneaded material was pressed for 30 minutes in a mold having a thickness of 0.38 mm under the conditions of 160 ° C. and 50 kg / cm ² to obtain a sheet A having a thickness of 0.38 mm. On the other hand, 100 parts by mass of PVB-3, 60 parts by mass of triethylene glycol di-2-ethylhexanoate as a plasticizer (Bp), and 0.2 parts by mass of triethylene glycol mono 2-as a dispersing agent (Bd). Ethyl hexanoate was kneaded in a Laboplast mill at 160 ° C. for 8 minutes. The obtained kneaded material was pressed for 30 minutes in a 0.15 mm thick mold at 160 ° C. and 50 kg / cm ² to obtain a sheet B having a thickness of 0.15 mm. Sheet A and Sheet B are stacked in the order of Sheet A / Sheet B / Sheet A, pressed and laminated in a 0.9 mm thick formwork at 135 ° C. and 10 kg / cm ² , and two more embossed sheets It is composed of A layer (0.38 mm) / B layer (0.14 mm) / A layer (0.38 mm) and measured according to ten-point average roughness Rz (JIS B0031-1994. The same was obtained). The ultraviolet absorbers used are shown in Table 6.

(Humidity control of high moisture content laminates)
The layered product-1 obtained above was conditioned for 12 hours in an atmosphere of 35 ° C. and 80% RH in a thermo-hygrostat. The humidity-adjusted laminate-1 was further conditioned under the following conditions (a), (b), and (c), and the humidity adjustment time was evaluated according to the following three-stage criteria. there were.
(conditions)
Condition (a): Treated at 23 ° C. and 28% RH for 18 hours.
Condition (b): treated at 29 ° C. and 55% RH for 18 hours, then treated at 23 ° C. and 28% RH for 18 hours.
Condition (c): treated with 32 ° C. and 68% RH for 18 hours, followed by treatment with 29 ° C. and 55% RH for 18 hours, followed by treatment with 26 ° C. and 40% RH for 18 hours, and finally Treated at 23 ° C. and 28% RH for 18 hours.
(Standard)
“18 hours”: The laminate does not cause white turbidity or delamination under the condition (a), and the moisture content is 0.7% or less.
“36 hours”: White turbidity or delamination occurs under the condition (a), but the laminate does not cause white turbidity or delamination under the condition (b), and the moisture content is 0.7% or less.
“72 hours”: Both of the conditions (a) and (b) cause white turbidity and delamination, but the laminate does not cause white turbidity or delamination under the condition (c), and the moisture content is 0.7%. What is below.

  “18 hours” of the above standard indicates that even if it is dried rapidly, water and plasticizer are not easily phase-separated from polyvinyl acetal in the laminate, and bleeding between layers of water and plasticizer hardly occurs. In addition, it indicates that more gradual drying is required as “36 hours” and “72 hours” are reached.

(Plasticizer bleed test at high water content)
The laminate-1 obtained above was dried at 23 ° C. and 28% RH for 5 days, and then treated in an atmosphere at 35 ° C. and 80% RH. Visual confirmation after 12 hours, 24 hours and 48 hours after the start of the treatment of the laminate-1 indicates that there is no plasticizer bleed after 12 hours and plasticizer bleed occurs after 24 hours. “12 hours”, when no plasticizer bleed occurs after 24 hours, and when plasticizer bleed occurs after 48 hours, “24 hours”, and when no plasticizer bleed occurs after 48 hours, “48 hours” , “48 hours”.

(Production of laminated glass)
30 cm × 30 cm laminate-1 was stored for 5 days in an atmosphere of 23 ° C. and 32% RH, and after humidity control, it was quickly sandwiched between two float glasses (30 cm × 30 cm × 2.2 mm). After heating to ° C., temporary bonding was performed using a nip roll. The obtained temporary adhesive body was put in an autoclave and treated for 60 minutes under conditions of 135 ° C. and 1.2 MPa to obtain a laminated glass-1. In the obtained laminated glass-1, no bubbles remained between the laminate and the glass.

(Hot water boiling test for laminated glass)
Laminated glass-1 was treated with hot water at 60 ° C. for 12 hours, and then treated in an atmosphere of 23 ° C. and 28% RH for 108 hours (this treatment is defined as one cycle). After repeating this process 10 times, from each end of the laminated glass, visually check for defects (exfoliation of the glass and the interlayer film for laminated glass, peeling of the interlayer of the interlayer film) due to extraction of components contained in the laminate. According to the above, it was evaluated as “none” when evaluated in three stages of “none”, “somewhat present”, and “present”.

(Evaluation of laminated glass: weather resistance)
The laminated glass-1 was subjected to an ultraviolet irradiation test, and the amount of change in the yellow index (YI) value of the laminated glass-1 before and after ultraviolet irradiation (that is, from the yellow index value after ultraviolet irradiation to the yellow index value before ultraviolet irradiation). minus), the amount of change in the b ^* value from (b ^* value after UV irradiation, a value obtained by subtracting the b ^* value before UV irradiation) was determined, respectively. Further, the state of discoloration at the edge of the laminated glass was visually observed and evaluated in three stages: “discolored”, “slightly discolored”, and “no discoloration”. In the ultraviolet irradiation test, Eye Super UV (SUV-F11) manufactured by Iwasaki Electric Co., Ltd. was used, and light of 295 to 450 nm was irradiated for 300 hours at a black panel temperature of 63 ° C. The yellow index (YI) value and b ^* value of the laminated glass were measured using a color meter (SM-T-H1 manufactured by Suga Test Instruments Co., Ltd.). The results are shown in Table 3.

(Handability when making laminated glass using vacuum back)
In Example 1 (preparation of laminate), except that the type of the embossed sheet was changed, it was similarly composed of A layer (0.38 mm) / B layer (0.14 mm) / A layer (0.38 mm). A laminate 1 (Rz10) having a 10-point average roughness Rz of 10 μm and a laminate-1 (Rz80) having a 10-point average roughness Rz of 80 μm were prepared.
The laminated body-1, laminated body-1 (Rz10) and laminated body-1 (Rz80) were each conditioned at 23 ° C. and 35% RH for 5 days and sandwiched between two pieces of glass having a thickness of 2 mm, followed by vacuum bags After being reduced in pressure to −0.095 atm, heated to 140 ° C. under reduced pressure and treated for 80 minutes, laminated glass V-1, laminated glass V-1 (Rz10) and laminated glass V-1 ( Rz80) was produced. Regarding these laminated glasses, when bubbles remained due to insufficient deaeration was visually confirmed, bubbles remained in the laminated glass V-1 (Rz10). Moreover, when the moisture content of the laminated body contained in each laminated glass was measured, it was 0.40% in the laminated body contained in the laminated glass V-1, and 0.8% in the laminated body contained in the laminated glass V-1 (Rz10). 48%, the laminated glass V-1 (Rz80) was 0.13%, and in the laminated glass V-1 (Rz80), the moisture content was remarkably reduced in the laminated glass production process. The moisture content was determined by smashing the glass with a hammer at a distance of 1 cm from the edge of each laminated glass and taking out the laminate quickly. Then, 0.5 g of the sample was Karl Fischer manufactured by Mitsubishi Chemical Analytical Co., Ltd. Using a moisture meter (used in combination with KF-200 (capacitance method moisture meter) and VA-200 (moisture vaporizer)), the sample was heated at 200 ° C. for 10 minutes, and the moisture evaporated during the measurement was measured. .
From the above, in Laminate-1, Laminate-1 (Rz10), and Laminate-1 (Rz80), Laminate-1 having a 10-point average roughness Rz of 35 μm has both degassing properties and moisture content controllability. It was suitable from the viewpoint.
In addition, as a result of performing the same evaluation in Examples 13, 14 and 16, which will be described later, in each case, the laminate having a 10-point average roughness Rz of 35 μm is from the viewpoint of coexistence of deaeration and moisture content controllability. A favorable result was shown.

(Examples 2 to 23, Comparative Examples 1 to 16)
A laminated body and a laminated glass were produced in the same manner as in Example 1 except that the compositions of the A layer and the B layer were changed as shown in Table 2 and Table 4, and evaluated in the same manner. The results are shown in Table 3 and Table 5. Moreover, the ultraviolet absorber used is shown in Table 6 or Table 7.

  As shown in the examples and comparative examples, the laminate of the present invention has a high water content at high temperature and high humidity, and then water in the laminate even when rapidly dried in an atmosphere of low temperature and low humidity. And the plasticizer is difficult to phase separate from the polyvinyl acetal and does not cause water or plasticizer bleeding between the layers of the laminate. Moreover, the laminated body of this invention can suppress coloring of a laminated body even when it is a case where ultraviolet irradiation is performed.

  The reason why the laminate of the present invention exhibits such characteristics is unknown, but the mass ratio of the content of the dispersant (Ad) to the content of the plasticizer (Ap) in the A layer is the plasticizer (Bp) in the B layer. When the moisture content of the laminate in which the outermost layers are both A layers is preferably high, it is caused by being larger than the mass ratio of the content of the dispersant (Bd) to the content of It is considered that the moisture content of the B layer also decreases before phase separation or bleed occurs as a result of moisture transferring from the B layer to the A layer as the water volatilizes.

The laminated body of the present invention is such that the plasticizer contained in the laminated body is difficult to be extracted and volatilized by water, and even if the laminated body having a high water content is rapidly dried in an atmosphere of low temperature and low humidity, And the plasticizer is difficult to phase separate from the polyvinyl acetal, and bleeding between layers of water and the plasticizer is difficult to occur. Further, even when used as an interlayer film for laminated glass over a long period of time, coloring is unlikely to occur and the durability is excellent.

Claims (19)

Polyvinyl acetal (A) having an average residual hydroxyl amount of X (mol%), an A layer containing a plasticizer (Ap) and a dispersant (Ad), and a polyvinyl acetal having an average residual hydroxyl group amount of Y (mol%) ( B) and a plasticizer (Bp), and a B layer which may contain a dispersant (Bd),
X ≧ Y,
The layer A further contains a benzotriazole-based ultraviolet absorber,
The mass ratio of the content of the dispersant (Ad) to the content of the plasticizer (Ap) in the A layer is the mass ratio of the content of the dispersant (Bd) to the content of the plasticizer (Bp) in the B layer. Bigger,
The plasticizer (Ap) is an ester compound having a chemical structure obtained by an esterification reaction of one molecule of m-valent alcohol (m represents a natural number of 2 to 4) and m molecule of a monovalent carboxylic acid having 8 to 20 carbon atoms. Yes,
The dispersant (Ad) has a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Ap), and (m-1) to 1 hydroxyl group and 1 to (m-1) A compound having an ester bond,
The plasticizer (Bp) is an ester compound having a chemical structure obtained by esterification reaction of one molecule of n-valent alcohol (n represents a natural number of 2 to 4) and n molecule of monovalent carboxylic acid having 8 to 20 carbon atoms. Yes,
The dispersant (Bd) has a chemical structure obtained by hydrolyzing at least one ester bond of the plasticizer (Bp), and has (n-1) to 1 hydroxyl group and 1 to (n-1) A compound having an ester bond,
Laminated body. A benzotriazole-based ultraviolet absorber has the formula (1):

Or a compound having the structure shown in formula (1), wherein at least one of hydrogen atoms bonded to any carbon atom in formula (1) is substituted with a substituent. Item 2. The laminate according to Item 1. The laminate according to claim 2, wherein at least one of the substituents is a hydrocarbon group having 4 to 8 carbon atoms. The laminate according to claim 2 or 3, wherein the benzotriazole ultraviolet absorber is a compound having two or more substituents. The laminate according to any one of claims 2 to 4, wherein the benzotriazole-based ultraviolet absorber is a compound having a substituent at the ortho position of the hydroxyl group in the aromatic ring to which the hydroxyl group in Formula (1) is bonded. The laminated body in any one of Claims 1-5 whose molecular weight of a benzotriazole type ultraviolet absorber is 300-800. The laminate according to any one of claims 1 to 6, wherein the m-valent alcohol is an ethylene glycol condensate having a condensation degree of 3 to 20. The laminate according to any one of claims 1 to 7, wherein the n-valent alcohol is a condensate of ethylene glycol having a condensation degree of 3 to 20. The laminated body in any one of Claims 1-8 whose average amount of residual hydroxyl groups X of polyvinyl acetal (A) is 20-40 mol%. The laminated body according to any one of claims 1 to 9, wherein the average residual hydroxyl group amount Y of the polyvinyl acetal (B) is 10 to 35 mol%, and the average residual vinyl ester group amount is 0.01 to 25 mol%. . Content of the plasticizer (Ap) with respect to 100 mass parts of polyvinyl acetal (A) in A layer is less than content of the plasticizer (Bp) with respect to 100 mass parts of polyvinyl acetal (B) in B layer. The laminated body in any one of. The laminate according to any one of claims 1 to 11, wherein the content of the plasticizer (Ap) in the A layer is 20 to 60 parts by mass with respect to 100 parts by mass of the polyvinyl acetal (A). The laminated body in any one of Claims 1-12 whose content of the plasticizer (Bp) in B layer is 30-80 mass parts with respect to 100 mass parts of polyvinyl acetal (B). The laminate according to any one of claims 1 to 13, wherein the monovalent carboxylic acid has at least two organic groups other than a carbonyl group bonded to carbon adjacent to the carboxyl group. The laminate according to any one of claims 1 to 14, which is a laminate comprising three or more layers, and at least one of the two outer layers of the laminate is an A layer. The laminated body in any one of Claims 1-15 which has an uneven structure in at least one surface. The laminated body according to claim 16, wherein the ten-point average roughness Rz of at least one of the surfaces having an uneven structure is 30 to 70 µm. The laminated body in any one of Claims 1-17 whose water content is 0.5 mass% or more and less than 0.65 mass%. Laminated glass comprising the laminate according to any one of claims 1 to 18.