WO2015059831A1

WO2015059831A1 - Multilayer film and intermediate film for laminated glass formed of same

Info

Publication number: WO2015059831A1
Application number: PCT/JP2013/079023
Authority: WO
Inventors: 楠藤　健; 太我油井
Original assignee: 株式会社クラレ
Priority date: 2013-10-25
Filing date: 2013-10-25
Publication date: 2015-04-30
Also published as: JPWO2015059831A1; JP5469287B1

Abstract

A multilayer film which has a layer (X) that contains a polyvinyl acetal (I) having an acetalization degree of 55-80% by mole, a content of a vinyl ester monomer unit of 0.1-1.5% by mole and a viscosity-average polymerization degree of 1,400-5,000, an ultraviolet absorbent and a plasticizer, and a layer (Y) that contains a polyvinyl acetal (II) having an acetalization degree of 70-85% by mole, a content of a vinyl ester monomer unit of 5-15% by mole and a viscosity-average polymerization degree of 1,400-5,000, heat blocking fine particles, a surfactant, an alkali metal salt and/or an alkaline earth metal salt, and a plasticizer, and wherein the layer (X) is arranged on both outer surfaces of the layer (Y). This multilayer film satisfies formulae (1) and (2). (A - B)/A < 0.80 (1) 1.00 × 10^-2 < (b/y)/(a/x) < 2.00 × 10^-1 (2) Consequently, there can be provided a film which has sufficient heat blocking performance, sufficient sound absorption performance, reduced inclusion of foreign substances (unsolved contents) and excellent recyclability, while being suppressed in coloration caused by heating.

Description

Multilayer film and interlayer film for laminated glass comprising the same

The present invention relates to a multilayer film having heat ray shielding properties and sound insulation properties. The present invention also relates to an interlayer film for laminated glass comprising the multilayer film, and a laminated glass using the interlayer film. Furthermore, this invention relates to the manufacturing method of the film using the recovered material of the said multilayer film.

Polyvinyl acetal is obtained by an acetalization reaction in water under acidic conditions using polyvinyl alcohol (hereinafter sometimes abbreviated as “PVA”) and an aldehyde compound. Polyvinyl acetal films are used in various applications because they are tough and have a unique structure that has both hydrophilic hydroxy groups and hydrophobic acetal groups. Various polyvinyl acetals have been proposed. Yes. Among them, polyvinyl formal produced from PVA and formaldehyde, polyvinyl acetal in a narrow sense produced from PVA and acetaldehyde, and polyvinyl butyral produced from PVA and butyraldehyde occupy commercially important positions.

In particular, polyvinyl butyral is widely used as an interlayer film for laminated glass of automobiles and buildings, and occupies a particularly important position commercially.

On the other hand, polyvinyl acetal has a problem that it is easily colored by heating; a foreign substance (undissolved part) is likely to be generated in the polyvinyl acetal film. Various proposals have been made to solve these problems.

Patent Documents 1 and 2 describe a method for suppressing coloring of polyvinyl acetal by acetalization at a specific hydroxide ion concentration under high temperature and high pressure. Patent Document 3 describes a method of suppressing coloring of the obtained polyvinyl acetal by adding a reducing agent after neutralization by acetalization reaction. However, foreign matters were liable to occur in the film produced using the polyvinyl acetal obtained by the methods described in Patent Documents 1 to 3. Patent Document 4 describes a method of suppressing the generation of coarse particles by adjusting the concentration of the obtained resin particle slurry in the neutralization reaction after the acetalization reaction. Patent Document 5 describes a method for suppressing the generation of coarse particles by defining the relationship between an acid catalyst and a surfactant used in the acetalization reaction. However, foreign matters were likely to be generated in the film produced using the polyvinyl acetal obtained by the methods described in Patent Documents 4 and 5. Moreover, the film was easily colored by heating. For these reasons, there is a strong demand for polyvinyl acetals in which all the above-mentioned problems are solved.

In recent years, various highly functional products have been developed for use in interlayer films for laminated glass. For example, for the purpose of imparting high sound insulation performance and heat insulation performance to the interlayer film for laminated glass, a plurality of polyvinyl acetal layers having different content ratios of polyvinyl acetal and plasticizer are laminated, and the central layer is made of heat ray shielding particles. An interlayer film for laminated glass is disclosed (see, for example, Patent Documents 6 to 9). In the interlayer film for multi-layer laminated glass, generally, polyvinyl acetals having different average residual hydroxyl groups are used for each layer in order to make the amount of plasticizer contained in each layer different.

Incidentally, the interlayer film for laminated glass is generally manufactured using an extruder from the viewpoint of production cost. The interlayer film for laminated glass is produced by a coextrusion method. When producing an interlayer film for laminated glass using these methods, a certain amount of trim material is generated at the edge of the film, and there are also off-spec products that are difficult to use as products due to non-uniform composition and thickness. can get.

When recycling the trim or off-spec product of the interlayer film for single-layer laminated glass, there were problems that the resulting film was colored by heating and that foreign matter (undissolved part) was generated in the obtained film. On the other hand, when recycling trim and off-spec products for multi-layer laminated glass with different compositions in each layer, in addition to these problems, each component is difficult to be compatible, so there is a problem that transparency is lowered. there were. In particular, when recycling the interlayer film for laminated glass provided with the above-described sound insulation and heat insulation, it is difficult to dissolve polyvinyl acetals having different average residual hydroxyl groups constituting each layer. Therefore, the obtained interlayer film for laminated glass has a problem inferior in transparency. In addition, when the intermediate film is recycled, it is difficult to redisperse the heat ray shielding particles in the center layer. This also contributed to the deterioration of transparency.

From the viewpoint of recent energy saving and effective use of resources, improving the yield of the entire film manufacturing process is a very important issue. Therefore, recycling of an interlayer film for multilayer laminated glass containing heat ray shielding particles, which has been difficult until now, is also demanded, and a solution to the above-described problems is desired.

JP 2011-219670 A JP 2011-219671 A Japanese Patent Laid-Open No. 5-140211 JP-A-5-155915 JP 2002-069126 A JP 2003-252657 A WO2008-122608 JP 2004-143008 A WO2012-077689

The present invention has been made in order to solve the above-mentioned problems, has sufficient heat ray shielding and sound insulation properties, has little coloration due to heating, has less foreign matter (undissolved content), and is recyclable. Another object of the present invention is to provide an excellent multilayer film. Moreover, it aims at providing the laminated glass which used the said multilayer film as an intermediate film. Furthermore, it aims at providing the manufacturing method of the film using the recovered material of the said multilayer film.

The above-mentioned problem is that a polyvinyl acetal having a degree of acetalization of 55 to 80 mol%, a vinyl ester monomer unit content of 0.1 to 1.5 mol% and a viscosity average polymerization degree of 1400 to 5000 (I ), An ultraviolet absorber and a plasticizer-containing layer (X), the degree of acetalization is 70 to 85 mol%, the content of vinyl ester monomer units is 5 to 15 mol%, and the viscosity average polymerization degree A layer (Y) containing polyvinyl acetal (II) having a particle size of 1400 to 5000, a heat ray shielding fine particle, a surfactant, an alkali metal salt and / or an alkaline earth metal salt, and a plasticizer. This is solved by providing a multilayer film in which the layers (X) are disposed on both outer sides of the following formulas (1) and (2).
(AB) / A <0.80 (1)
1.00 × 10 ⁻² <(b / y) / (a / x) <2.00 × 10 ⁻¹ (2)

Where
A: The peak top of the polymer component measured by a differential refractive index detector when the multilayer film heated at 230 ° C. for 3 hours was measured by gel permeation chromatography (hereinafter sometimes abbreviated as GPC). Molecular weight a: Signal intensity at peak top molecular weight (A) B: Peak of polymer component measured by an absorptiometric detector (measurement wavelength 280 nm) when the multilayer film heated at 230 ° C. for 3 hours is measured by GPC Top molecular weight b: Signal intensity at peak top molecular weight (B) x: Differential refractive index detector when GPC measurement of monodispersed polymethyl methacrylate (hereinafter, polymethyl methacrylate may be abbreviated as PMMA) Signal strength y at peak top molecular weight measured by: monodispersed PMMA When the GPC measurement, a signal intensity at the peak top molecular weight measured by spectrophotometric detector (measuring wavelength 220 nm).

However, in GPC measurement of multilayer film and PMMA,
Mobile phase: 20 mmol / l sodium trifluoroacetate-containing hexafluoroisopropanol (hereinafter, hexafluoroisopropanol may be abbreviated as HFIP.)
Sample concentration: 1.00 mg / ml
Sample injection volume: 100 μl
Column temperature: 40 ° C
Flow rate: 1.0 ml / min.

It is preferable that the multilayer film satisfies the following formulas (3) and (4).
(AC) / A <0.80 (3)
5.00 × 10 ⁻³ <(c / y) / (a / x) <7.00 × 10 ⁻² (4)

Where
A: Same as the above formula (1), a, x, y: Same as the above formula (2) C: Absorbance detector (measurement wavelength when GPC measurement is performed on the multilayer film heated at 230 ° C. for 3 hours) Peak top molecular weight c of the polymer component measured at 320 nm): signal intensity at peak top molecular weight (C).

The polyvinyl acetal (I) and the polyvinyl acetal (II) are preferably polyvinyl butyral (hereinafter sometimes abbreviated as PVB).

An interlayer film for laminated glass made of the multilayer film is a preferred embodiment of the present invention. A laminated glass formed by bonding a plurality of glass plates using the interlayer film for laminated glass is also a preferred embodiment of the present invention.

A method for producing a single-layer film in which the collected product of the multilayer film is melt-kneaded and then formed is also a preferred embodiment of the present invention. At this time, the recovered product was a polyvinyl acetal having a degree of acetalization of 55 to 85 mol%, a vinyl ester monomer unit content of 0.1 to 15 mol%, and a viscosity average polymerization degree of 1400 to 5000 ( It is more preferable to form a film after melt-kneading III) and the plasticizer.

Collected product of the multilayer film, polyvinyl acetal having an acetalization degree of 55 to 85 mol%, a vinyl ester monomer unit content of 0.1 to 15 mol%, and a viscosity average polymerization degree of 1400 to 5000 (III) Polyvinyl acetal on both outer sides of the layer (Y ′) formed by melt-kneading the plasticizer, heat ray shielding fine particles, surfactant, and alkali metal salt and / or alkaline earth metal salt. A method for producing a multilayer film in which the layer (X) formed by melt-kneading (I), an ultraviolet absorber and a plasticizer and then forming a film is also a preferred embodiment of the present invention.

The multilayer film of the present invention has sufficient heat ray shielding and sound absorbing properties, is less colored by heating, has less foreign matter (undissolved content), and is excellent in recyclability. Therefore, the multilayer film is useful as an interlayer film for laminated glass. Furthermore, the film obtained by the manufacturing method using the recovered material of the multilayer film has excellent transparency since it is less colored and has less foreign matter (undissolved content).

In the multilayer film of the present invention, the relationship between the molecular weight and the value measured by the differential refractive index detector (RI), and the relationship between the molecular weight and the absorbance measured by the absorptiometric detector (UV) (measurement wavelength 280 nm). It is the graph which showed.

The multilayer film of the present invention has an acetalization degree of 55 to 80 mol%, a vinyl ester monomer unit content of 0.1 to 1.5 mol%, and a viscosity average polymerization degree of 1400 to 5000. A layer (X) containing polyvinyl acetal (I), an ultraviolet absorber, and a plasticizer, an acetalization degree of 70 to 85 mol%, and a vinyl ester monomer unit content of 5 to 15 mol% A layer (Y) containing polyvinyl acetal (II) having a viscosity average polymerization degree of 1400 to 5000, heat ray shielding fine particles, surfactant, alkali metal salt and / or alkaline earth metal salt, and plasticizer The layer (X) is disposed on both outer sides of the layer (Y) and satisfies the following formulas (1) and (2).
(AB) / A <0.80 (1)
1.00 × 10 ⁻² <(b / y) / (a / x) <2.00 × 10 ⁻¹ (2)

Where
A: When the multilayer film heated at 230 ° C. for 3 hours is subjected to GPC measurement, the peak top molecular weight of the polymer component measured by the differential refractive index detector a: the signal intensity B at the peak top molecular weight (A) B: 230 When the multilayer film heated at 3 ° C. for 3 hours is subjected to GPC measurement, the peak top molecular weight b of the polymer component measured by an absorptiometric detector (measurement wavelength 280 nm): signal intensity x at peak top molecular weight (B): Signal intensity y at the peak top molecular weight measured with a differential refractive index detector when monodispersed PMMA is measured by GPC: with an absorptiometric detector (measurement wavelength 220 nm) when the monodispersed PMMA is measured by GPC Signal intensity at the measured peak top molecular weight.

However, in GPC measurement of multilayer film and PMMA,
Mobile phase: HFIP containing 20 mmol / l sodium trifluoroacetate
Sample concentration: 1.00 mg / ml
Sample injection volume: 100 μl
Column temperature: 40 ° C
Flow rate: 1.0 ml / min.

In the GPC measurement in the present invention, a GPC apparatus having a differential refractive index detector and an absorptiometric detector and capable of simultaneously performing measurement by these detectors is used. The cell of the detection part of the absorptiometric detector preferably has a cell length (optical path length) of 10 mm. The absorptiometric detector may measure the absorption of ultraviolet light having a specific wavelength, or may measure the absorption of ultraviolet light having a specific range of wavelengths. The multilayer film subjected to the measurement is separated into each molecular weight component by a GPC column. The signal intensity by the differential refractive index detector is approximately proportional to the concentration (g / l) of the film component. On the other hand, the components detected by the absorptiometric detector are only those having a structure that absorbs a predetermined wavelength. By the GPC measurement, the concentration and absorbance at a predetermined wavelength can be measured for each molecular weight component of the film.

HFIP containing sodium trifluoroacetate having a concentration of 20 mmol / l is used as a solvent and a mobile phase used for dissolving the multilayer film and PMMA measured in the GPC measurement. HFIP can dissolve the multilayer film and PMMA of the present invention. Further, by adding sodium trifluoroacetate, adsorption of film components and PMMA to the column filler is prevented. The flow rate and column temperature in the GPC measurement are appropriately adjusted according to the type of column used. The flow rate in the GPC measurement is usually 1.0 ml / min, and the column temperature is usually 40 ° C.

The GPC column used in the GPC measurement is not particularly limited as long as it can separate the components in the multilayer film of the present invention for each molecular weight. Specifically, “GPC HFIP-806M” manufactured by Showa Denko KK is preferably used.

In the present invention, standard PMMA is monodispersed PMMA. As the standard PMMA, monodispersed PMMA, which is usually used as a standard for preparing a calibration curve for molecular weight measurement by GPC measurement, can be used. Several types of standard PMMA with different molecular weights are measured, and a calibration curve is created from the GPC elution volume and the molecular weight of the standard PMMA. In the present invention, a calibration curve prepared using the detector is used for the measurement with the differential refractive index detector, and a calibration prepared using the detector (measurement wavelength: 220 nm) for the measurement with the absorptiometric detector. Use lines. Using these calibration curves, the GPC elution volume is converted into the molecular weight, and the peak top molecular weight (A) and the peak top molecular weight (B) are determined.

Before the GPC measurement, the multilayer film is heated at 230 ° C. for 3 hours. In the present invention, the multilayer film is heated by the following method. The multilayer film is heated by hot pressing for 3 hours at a pressure of 2 MPa and 230 ° C. Thereby, the difference in the hue of the sample after the heat treatment is clearly reflected in the difference in the absorbance (that is, the signal intensity detected by the absorptiometric detector). The thickness of the film to be heated is 600 to 800 μm, preferably about 760 μm, which is the thickness of a normal laminated glass interlayer.

A measurement sample is obtained by dissolving the heated multilayer film in the above-mentioned solvent (HFIP containing sodium trifluoroacetate). The concentration of the measurement sample is 1.00 mg / ml, and the injection volume is 100 μl. However, when the viscosity average polymerization degree of the polyvinyl acetal (I) or the polyvinyl acetal (II) in the multilayer film exceeds 2400, the excluded volume increases. Therefore, when the concentration of the measurement sample is 1.00 mg / ml, the reproducibility is good. Measurement may not be possible. In that case, an appropriately diluted sample (injection amount 100 μl) is used. The signal intensity detected by the absorptiometric detector and the differential refractive index detector is proportional to the concentration of the sample. Therefore, the concentration of the diluted sample and the actually measured signal intensity are used to convert each signal intensity when the concentration of the measurement sample is 1.00 mg / ml.

FIG. 1 shows the relationship between the molecular weight obtained by GPC measurement of the multilayer film of the present invention and the signal intensity measured with a differential refractive index detector, and the molecular weight measured with an absorptiometric detector (measurement wavelength 280 nm). It is the graph which showed the relationship with the signal intensity (absorbance). The GPC measurement in the present invention will be further described with reference to FIG. In FIG. 1, the chromatogram indicated by “RI” is a plot of the signal intensity measured by the differential refractive index detector against the molecular weight (horizontal axis) of the film component converted from the elution volume. The peak seen in the chromatogram near the molecular weight of 100,000 is the peak of the polymer component. In the present invention, the molecular weight at the peak position of such a polymer component is defined as the peak top molecular weight (A) of the polymer component, and the signal intensity at the peak top molecular weight (A) is defined as the signal intensity (a). Since the film of the present invention contains polyvinyl acetal having a viscosity average degree of polymerization of 1400 to 5000, the peak top molecular weight (A) of the polymer component usually exceeds 3500. In addition, in FIG. 1, the peak seen in the molecular weight 1500 vicinity is a peak of the plasticizer contained in a film. When there are a plurality of peaks having a peak top molecular weight exceeding 3500 in the chromatogram, the molecular weight at the peak position having the highest peak height is defined as the peak top molecular weight (A).

In FIG. 1, the chromatogram indicated by “UV” shows the signal intensity (absorbance) measured with an absorptiometric detector (measurement wavelength 280 nm) with respect to the molecular weight (horizontal axis) of the film component converted from the elution volume. It is a plot. The peak seen in the chromatogram near the molecular weight of 50,000 is the peak of the polymer component. In the present invention, the molecular weight at the peak position of such a polymer component is defined as the peak top molecular weight (B) of the polymer component, and the signal intensity (absorbance) at the peak top molecular weight (B) is defined as the signal intensity (b). Since the multilayer film of the present invention contains polyvinyl acetal (I) and polyvinyl acetal (II) having a viscosity average polymerization degree of 1400 to 5000, the peak top molecular weight (B) of the polymer component usually exceeds 3500. When there are a plurality of peaks having a peak top molecular weight exceeding 3500 in the chromatogram, the molecular weight at the peak position having the highest peak height is defined as the peak top molecular weight (B).

The multilayer film of the present invention is measured by the peak top molecular weight (A) of the polymer component measured by the differential refractive index detector and measured by the absorptiometric detector (measurement wavelength 280 nm) when GPC measurement is performed by the method described above. The peak top molecular weight (B) of the polymer component to be satisfied satisfies the following formula (1).
(AB) / A <0.80 (1)

The peak top molecular weight (A) is a value serving as an index of the molecular weight of the polymer component in the multilayer film. On the other hand, the peak top molecular weight (B) is derived from a component having absorption at 280 nm, which is present in the polymer component. Usually, since the peak top molecular weight (A) is larger than the peak top molecular weight (B), (AB) / A becomes a positive value. As the peak top molecular weight (B) increases, (AB) / A decreases, and as the peak top molecular weight (B) decreases, (AB) / A increases. That is, when (AB) / A is large, it means that the low molecular weight component in the polymer component contains many components that absorb ultraviolet light having a wavelength of 280 nm.

When (AB) / A is 0.80 or more, as described above, the low molecular weight component contains more components that absorb ultraviolet light having a wavelength of 280 nm. In this case, the foreign matter (undissolved part) in the obtained multilayer film increases. For this reason, foreign matter (undissolved content) in the film produced by using the recovered material (trim, off-spec product, etc.) of the multilayer film also increases, and the transparency of the film decreases. (AB) / A is preferably less than 0.75, more preferably less than 0.70.

The multilayer film of the present invention satisfies the following formula (2).
1.00 × 10 ⁻² <(b / y) / (a / x) <2.00 × 10 ⁻¹ (2)

In the formula (2), a is the signal intensity measured by the differential refractive index detector at the peak top molecular weight (A) in the GPC measurement. b is the signal intensity (absorbance) measured with an absorptiometric detector (measurement wavelength 280 nm) at the peak top molecular weight (B).

In the formula (2), x is the signal intensity at the peak top molecular weight measured by the differential refractive index detector when monodispersed PMMA is measured by GPC. y is the signal intensity (absorbance) at the peak top molecular weight measured with an absorptiometer (measurement wavelength 220 nm) when the monodispersed PMMA is measured by GPC. The GPC measurement of monodispersed PMMA is the same as the GPC measurement of the aforementioned multilayer film except that monodispersed PMMA is used instead of the heated multilayer film and the measurement wavelength of the spectrophotometric detector is changed to 220 nm. Perform in the same way. The signal intensity (x) is obtained in the same manner as the signal intensity (a). The signal intensity (y) is obtained in the same manner as the signal intensity (b). As the monodispersed PMMA used for obtaining x and y, PMMA having a weight average molecular weight of about 85,000 is preferable.

(B / y) / (a / x) is an index of the content of a component having a structure that absorbs ultraviolet light having a wavelength of 280 nm in the polymer component of the multilayer film. When this value is large, it means that the content is large. As described above, the signal intensity by the differential refractive index detector is approximately proportional to the concentration (g / l) of the film component. On the other hand, what is detected by the absorptiometric detector is only the component having absorption at 280 nm which is the measurement wavelength, and the signal intensity (absorbance) by the absorptiometric detector is proportional to the concentration of the component having absorption at 280 nm. . Usually, the signal intensity of the differential refractive index detector is indicated by “millivolt”, and the signal intensity (absorbance) of the absorptiometric detector is indicated by “absorbance unit (AU)”.

However, since the signal intensity (a) measured by the differential refractive index detector and the signal intensity (b) obtained by the absorptiometric detector differ depending on the model of the GPC apparatus and the measurement conditions, the ratio of both is simply compared. It ’s difficult. On the other hand, in the present invention, as described below, the ratio of the signal intensity obtained by the differential refractive index detector and the signal intensity obtained by the absorptiometric detector is not different depending on the model of the GPC apparatus and the measurement conditions. Desired.

In the present invention, the ratio (a / x) of the signal intensity (a) of the multilayer film by the differential refractive index detector to the signal intensity (x) of monodispersed PMMA by the differential refractive index detector, and by the absorptiometric detector The ratio (b / y) of the signal intensity (b) of the multilayer film by the absorptiometric detector to the signal intensity (y) of monodispersed PMMA is determined. And ratio (b / y) / (a / x) of both is calculated | required and this is made into the parameter | index of content of the component which has a structure which absorbs ultraviolet light with a wavelength of 280 nm. Thus, by using the signal intensity of monodispersed PMMA as a reference, the same index can be used for evaluation regardless of the device model and measurement conditions.

The multilayer film of the present invention preferably satisfies the following formula (2 ′), and more preferably satisfies the following formula (2 ″).
1.50 × 10 ⁻² <(b / y) / (a / x) <1.50 × 10 ⁻¹ (2 ′)
2.00 × 10 ⁻² <(b / y) / (a / x) <1.00 × 10 ⁻¹ (2 ″)

When (b / y) / (a / x) is 1.00 × 10 ⁻² or less, as described above, the polymer component of the multilayer film contains few components that absorb ultraviolet light having a wavelength of 280 nm. Therefore, the foreign material (undissolved part) in a multilayer film increases. Therefore, the foreign material (undissolved part) in the film manufactured using the collection | recovery of the said multilayer film also increases, and the transparency of the said film falls. Conversely, when (b / y) / (a / x) is 2.00 × 10 ⁻¹ or more, the polymer component of the film has many components that absorb ultraviolet light having a wavelength of 280 nm. Therefore, the obtained multilayer film is colored by heating. Moreover, the film manufactured using the recovered material of the multilayer film is colored.

From the viewpoint of excellent balance between suppression of coloring and reduction of foreign matter (undissolved content) in the multilayer film of the present invention, the peak top molecular weight (A) measured with a differential refractive index detector in the GPC measurement, The peak top molecular weight (C) measured by an absorptiometric detector (measurement wavelength: 320 nm) is expressed by the following formula (3)
(AC) / A <0.80 (3)
It is preferable to satisfy.

The peak top molecular weight (C) is measured in the same manner as the peak top molecular weight (B) except that the measurement wavelength in the absorptiometric detector is 320 nm. The peak top molecular weight (C) is derived from a component having an absorption at 320 nm, which is present in the polymer component in the multilayer film. Usually, since the peak top molecular weight (A) is larger than the peak top molecular weight (C), (AC) / A becomes a positive value. As the peak top molecular weight (C) increases, (AC) / A decreases, and as the peak top molecular weight (C) decreases, (AC) / A increases. That is, when (AC) / A is large, it means that the low molecular weight component in the polymer component contains many components that absorb ultraviolet light having a wavelength of 320 nm.

When (AC) / A is 0.80 or more, as described above, the low molecular weight component contains more components that absorb ultraviolet rays having a wavelength of 320 nm. In this case, there is a possibility that foreign matter (undissolved content) in the obtained multilayer film increases. When the said foreign material (undissolved part) increases, the foreign material (undissolved part) in the film manufactured using the collection | recovery of a multilayer film may also increase, and there exists a possibility that the transparency of the said film may fall. (AC) / A is more preferably less than 0.75, and even more preferably less than 0.70.

The multilayer film of the present invention preferably satisfies the following formula (4).
5.00 × 10 ⁻³ <(c / y) / (a / x) <7.00 × 10 ⁻² (4)

In the formula (4), a, x and y are the same as the above formula (2). c is the signal intensity (absorbance) measured with an absorptiometric detector (measurement wavelength: 320 nm) at the peak top molecular weight (C).

Here, (c / y) / (a / x) is an index of the content of a component having a structure that absorbs ultraviolet light having a wavelength of 320 nm in the polymer component of the multilayer film. When this value is large, it means that the content is large. And it calculates | requires similarly to the above-mentioned (b / y) / (a / x) except the measurement wavelength in an absorptiometric detector being 320 nm.

The film of the present invention more preferably satisfies the following formula (4 ′), and more preferably satisfies the following formula (4 ″).
7.00 × 10 ⁻³ <(c / y) / (a / x) <6.00 × 10 ⁻² (4 ′)
^{1.00 × 10 -2 <(c /} y) / (a / x) <5.00 × 10 -2 (4 ")

When (c / y) / (a / x) is 5.00 × 10 ⁻³ or less, as described above, the polymer component of the multilayer film has few components that absorb ultraviolet light having a wavelength of 320 nm. Therefore, there is a possibility that foreign matter (undissolved part) in the multilayer film increases. When the said foreign material (undissolved part) increases, the foreign material (undissolved part) in the film manufactured using the collection | recovery of a multilayer film may also increase, and there exists a possibility that the transparency of the said film may fall. Conversely, when (c / y) / (a / x) is 7.00 × 10 ⁻² or more, the polymer component of the film has many components that absorb ultraviolet light having a wavelength of 320 nm. Therefore, the obtained multilayer film may be easily colored by heating. Moreover, there exists a possibility that the film manufactured using the collection | recovery of the said multilayer film may become easy to color.

In the present invention, the viscosity average degree of polymerization of polyvinyl acetal is represented by the viscosity average degree of polymerization of the raw material PVA measured according to JIS-K6726. That is, after re-saponifying and purifying PVA to a saponification degree of 99.5 mol% or more, it can be obtained from the intrinsic viscosity [η] measured in water at 30 ° C. by the following equation. The viscosity average polymerization degree of PVA and the viscosity average polymerization degree of polyvinyl acetal obtained by acetalizing it are substantially the same.
P = ([η] × 10000 / 8.29) ^{(1 / 0.62)}

The viscosity average polymerization degree of polyvinyl acetal (I) and polyvinyl acetal (II) is 1400 to 5000, and preferably 1500 to 3500. When the viscosity average degree of polymerization is less than 1400, the strength of the multilayer film is insufficient. On the other hand, when the polymerization degree exceeds 5000, the melt viscosity becomes too high and film formation becomes difficult.

The degree of acetalization of the polyvinyl acetal (I) used in the present invention is 55 to 80 mol%. When the degree of acetalization is less than 55 mol%, the compatibility with a plasticizer or the like decreases. Moreover, the foreign material (undissolved part) in a multilayer film increases. Moreover, the foreign material (undissolved part) in the film manufactured using the collection | recovery of the said multilayer film also increases, and the transparency of the said film falls. The degree of acetalization of the polyvinyl acetal (I) is preferably 60 mol% or more, more preferably 65 mol% or more. On the other hand, when the degree of acetalization exceeds 80 mol%, it may be easy to color. The degree of acetalization of the polyvinyl acetal (I) is preferably 75 mol% or less.

The degree of acetalization of the polyvinyl acetal (II) used in the present invention is 70 to 85 mol%. When the degree of acetalization exceeds 85 mol%, the efficiency of the acetalization reaction is significantly reduced. In addition, the multilayer film is colored by heating. Furthermore, the film manufactured using the recovered material of the multilayer film is also colored. The degree of acetalization of polyvinyl acetal (II) is preferably 80 mol% or less. On the other hand, when the degree of acetalization is less than 70 mol%, foreign matter (undissolved content) in the film may increase.

The difference between the degree of acetalization of polyvinyl acetal (I) and the degree of acetalization of polyvinyl acetal (II) from the point of excellent balance between the coloration resistance of the resulting multilayer film and the amount of foreign matter (undissolved) (II- I) is preferably 2 mol% or more, and more preferably 4 mol% or more.

In the present invention, the degree of acetalization represents the ratio of acetalized vinyl alcohol monomer units to the total monomer units constituting polyvinyl acetal. Among the vinyl alcohol monomer units in the raw material PVA, those that are not acetalized remain in the resulting polyvinyl acetal as vinyl alcohol monomer units.

The content of the vinyl ester monomer unit of polyvinyl acetal (I) used in the present invention is 0.1 to 1.5 mol%. When the content of the vinyl ester monomer unit is less than 0.1 mol%, the polyvinyl acetal cannot be stably produced and the film cannot be formed. The content of the vinyl ester monomer unit is preferably 0.3 mol% or more, more preferably 0.5 mol% or more, and further preferably 0.7 mol% or more. On the other hand, the content of the vinyl ester monomer unit is preferably 1.2 mol% or less.

The content of the vinyl ester monomer unit of polyvinyl acetal (II) used in the present invention is 5 to 15 mol%. When the content of the vinyl ester monomer unit exceeds 15 mol%, the resulting multilayer film is colored by heating. Furthermore, the film manufactured using the recovered material of the multilayer film is also colored. The content of the vinyl ester monomer unit of polyvinyl acetal (II) is preferably 13 mol% or less, more preferably 10 mol% or less. On the other hand, the content of the vinyl ester monomer unit is preferably 6 mol% or more, more preferably 7 mol% or more. When the content of the vinyl ester monomer unit of polyvinyl acetal (II) is in the above range, the layer (Y) becomes a soft layer, and the multilayer film of the present invention maintains a practical mechanical strength. , Has excellent sound insulation performance.

The content of the vinyl alcohol monomer unit of the polyvinyl acetal (I) used in the present invention is preferably 18.5 to 44.9 mol%. The content of the vinyl alcohol monomer unit in the polyvinyl acetal (II) used in the present invention is preferably 5 to 25 mol%.

Moreover, in this invention, content (mol%) of the vinyl alcohol monomer unit of polyvinyl acetal (I) is larger than content (mol%) of the vinyl alcohol monomer unit of polyvinyl acetal (II). It is preferable. The result that the affinity of the surfactant for the layer (Y) is higher than the affinity for the layer (X) by providing a difference in the content of the vinyl alcohol monomer units in the layer (X) and the layer (Y) The bleed-out of the surfactant can be effectively suppressed. The difference (I-II) between the content of the vinyl alcohol monomer unit of the polyvinyl acetal (I) and the content of the vinyl alcohol monomer unit of the polyvinyl acetal (II) is preferably 5 mol% or more, More preferably, it is 10 mol% or more. On the other hand, the difference (I-II) is preferably 30 mol% or less.

Content of monomer units other than acetalized monomer unit, vinyl ester monomer unit and vinyl alcohol monomer unit in polyvinyl acetal (I) and polyvinyl acetal (II) used in the present invention Is preferably 20 mol% or less, more preferably 10 mol% or less, and even more preferably 5 mol% or less.

The polyvinyl acetal (I) and polyvinyl acetal (II) used in the present invention are usually produced by acetalizing PVA.

The saponification degree of the raw material PVA used for the production of polyvinyl acetal is preferably 80 to 99.9 mol%, more preferably 82 to 99.7 mol%, still more preferably 85 to 99.5 mol%, Preferably, it is 87 to 99.3 mol%. When the saponification degree of raw material PVA is less than 80 mol%, the foreign material (undissolved part) in the obtained multilayer film may increase, or the obtained multilayer film may be easily colored by heating. On the other hand, when the degree of saponification exceeds 99.9 mol%, PVA may not be produced stably. The degree of saponification of PVA is measured according to JIS-K6726.

The raw material PVA may contain an alkali metal salt of carboxylic acid, and its content is preferably 0.50% by mass or less, more preferably 0.37% by mass or less, and 0.28% by mass in terms of the mass of the alkali metal. % Or less is more preferable, and 0.23 mass or less is particularly preferable. When the content of the alkali metal salt of the carboxylic acid in the raw material PVA exceeds 0.50% by mass, the resulting multilayer film may be easily colored. The content of alkali metal salt of carboxylic acid (calculated in terms of alkali metal mass) is obtained from the amount of alkali metal ions obtained by ashing PVA with a platinum crucible and then measuring the resulting ash content by ICP emission analysis. Can do.

Examples of vinyl ester monomers used in the production of raw material PVA include vinyl formate, vinyl acetate, vinyl propionate, vinyl valelate, vinyl caprate, vinyl laurate, vinyl stearate, vinyl benzoate, vinyl pivalate and versatic. Examples thereof include vinyl acid, and vinyl acetate is particularly preferable.

The raw material PVA can also be produced by polymerizing vinyl ester monomers in the presence of thiol compounds such as 2-mercaptoethanol, n-dodecyl mercaptan, mercaptoacetic acid, 3-mercaptopropionic acid, and saponifying the resulting polyvinyl ester. You can also By this method, PVA in which a functional group derived from a thiol compound is introduced at the terminal is obtained.

Examples of the method for polymerizing the vinyl ester monomer include known methods such as bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization. Among the methods, a bulk polymerization method performed without a solvent or a solution polymerization method performed using a solvent such as alcohol is usually employed. In terms of enhancing the effect of the present invention, a solution polymerization method in which polymerization is performed together with a lower alcohol is preferable. The lower alcohol is not particularly limited, but an alcohol having 3 or less carbon atoms such as methanol, ethanol, propanol and isopropanol is preferable, and methanol is usually used. When performing the polymerization reaction by the bulk polymerization method or the solution polymerization method, the reaction can be carried out by either a batch method or a continuous method. Examples of the initiator used in the polymerization reaction include 2,2′-azobisisobutyronitrile, 2,2′-azobis (2,4-dimethyl-valeronitrile), 2,2′-azobis (4-methoxy). Azo initiators such as -2,4-dimethylvaleronitrile); organic peroxide initiators such as benzoyl peroxide, n-propyl peroxycarbonate, peroxydicarbonate, etc., within a range that does not impair the effects of the present invention. A well-known initiator is mentioned. Among them, an organic oxide initiator having a half-life of 10 to 110 minutes at 60 ° C. is preferable, and peroxydicarbonate is particularly preferable. There is no particular limitation on the polymerization temperature for carrying out the polymerization reaction, but a range of 5 ° C to 200 ° C is suitable.

When the vinyl ester monomer is radically polymerized, a copolymerizable monomer can be copolymerized as necessary as long as the effects of the present invention are not impaired. Examples of such monomers include α-olefins such as ethylene, propylene, 1-butene, isobutene, 1-hexene; carboxylic acids such as fumaric acid, maleic acid, itaconic acid, maleic anhydride, itaconic anhydride, or the like Derivatives; acrylic acid or salts thereof; acrylic acid esters such as methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate; methacrylic acid or salts thereof; methyl methacrylate, ethyl methacrylate, n-methacrylate Methacrylic acid esters such as propyl and isopropyl methacrylate; Acrylamide derivatives such as acrylamide, N-methylacrylamide and N-ethylacrylamide; Derivatives of methacrylamide such as methacrylamide, N-methylmethacrylamide and N-ethylmethacrylamide Vinyl ethers such as methyl vinyl ether, ethyl vinyl ether, n-propyl vinyl ether, isopropyl vinyl ether, and n-butyl vinyl ether; vinyl group-containing vinyl ethers such as ethylene glycol vinyl ether, 1,3-propanediol vinyl ether, and 1,4-butanediol vinyl ether Allyl ethers such as allyl acetate, propyl allyl ether, butyl allyl ether, hexyl allyl ether; monomers having an oxyalkylene group; isopropenyl acetate, 3-buten-1-ol, 4-penten-1-ol, Hydroxy group-containing α-olefins such as 5-hexen-1-ol, 7-octen-1-ol, 9-decen-1-ol, 3-methyl-3-buten-1-ol; Monomers having a sulfonic acid group such as phonic acid, allylsulfonic acid, methallylsulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid; vinyloxyethyltrimethylammonium chloride, vinyloxybutyltrimethylammonium chloride, vinyloxyethyl Cationic groups such as dimethylamine, vinyloxymethyldiethylamine, N-acrylamidomethyltrimethylammonium chloride, N-acrylamidoethyltrimethylammonium chloride, N-acrylamidodimethylamine, allyltrimethylammonium chloride, methallyltrimethylammonium chloride, dimethylallylamine, allylethylamine Monomers having a vinyl trimethoxysilane, vinylmethyldimethoxysilane, Monomers having a silyl group such as xylsilane, vinyltriethoxysilane, vinylmethyldiethoxysilane, vinyldimethylethoxysilane, 3- (meth) acrylamide-propyltrimethoxysilane, 3- (meth) acrylamide-propyltriethoxysilane Etc. The amount of the monomer that can be copolymerized with these vinyl ester monomers varies depending on the purpose and use of the monomer, but is usually based on all monomers used for copolymerization. Is 20 mol% or less, preferably 10 mol% or less, and more preferably 5 mol% or less.

PVA is obtained by saponifying the polyvinyl ester obtained by the above method in an alcohol solvent.

As the catalyst for the saponification reaction of polyvinyl ester, an alkaline substance is usually used, and examples thereof include alkali metal hydroxides such as potassium hydroxide and sodium hydroxide, and alkali metal alkoxides such as sodium methoxide. The amount of the alkaline substance used is preferably in the range of 0.002 to 0.2 in the molar ratio based on the vinyl ester monomer unit of the polyvinyl ester, and in the range of 0.004 to 0.1. It is particularly preferred. The saponification catalyst may be added all at once in the early stage of the saponification reaction, or a part thereof may be added in the early stage of the saponification reaction, and the rest may be added during the saponification reaction.

Examples of the solvent that can be used for the saponification reaction include methanol, methyl acetate, dimethyl sulfoxide, diethyl sulfoxide, and dimethylformamide. Of these solvents, methanol is preferably used. In its use, the water content of methanol is preferably adjusted to 0.001 to 1% by weight, more preferably 0.003 to 0.9% by weight, and particularly preferably 0.005 to 0.8% by weight.

The saponification reaction is preferably performed at a temperature of 5 to 80 ° C., more preferably 20 to 70 ° C. The time required for the saponification reaction is preferably 5 minutes to 10 hours, more preferably 10 minutes to 5 hours. The saponification reaction can be carried out by either a batch method or a continuous method. After completion of the saponification reaction, the remaining saponification catalyst may be neutralized as necessary. Usable neutralizing agents include organic acids such as acetic acid and lactic acid, and ester compounds such as methyl acetate.

The alkaline substance containing an alkali metal added during the saponification reaction is usually neutralized by an ester such as methyl acetate produced by the progress of the saponification reaction, or neutralized by adding a carboxylic acid such as acetic acid. At this time, an alkali metal salt of a carboxylic acid such as sodium acetate is formed. As described above, the raw material PVA preferably contains a predetermined amount of an alkali metal salt of carboxylic acid.

In order to obtain such a PVA, the PVA may be washed with a washing solution containing a lower alcohol such as methanol after saponification. The cleaning liquid may contain 20 parts by mass or less of water with respect to 100 parts by mass of the lower alcohol. Moreover, the said washing | cleaning liquid may contain ester, such as methyl acetate produced | generated in a saponification process. The content of the ester at this time is not particularly limited, but is preferably 1000 parts by mass or less with respect to 100 parts by mass of the lower alcohol. The amount of the cleaning solution used for cleaning is preferably 100 parts by weight to 10000 parts by weight, more preferably 150 parts by weight to 5000 parts by weight, with respect to 100 parts by weight of the gel obtained by saponification and PVA swollen with alcohol. More preferably, it is 200 to 1000 parts by mass. When the addition amount of the cleaning liquid is less than 100 parts by mass, the alkali metal salt amount of the carboxylic acid may exceed the above range. On the other hand, when the addition amount of the cleaning liquid exceeds 10,000 parts by mass, the improvement of the cleaning effect by increasing the addition amount cannot be expected. The washing method is not particularly limited. For example, PVA (swelled gel) and a washing solution are added to a tank, and the solution is stirred or allowed to stand for 5 to 180 minutes at 5 to 100 ° C. to remove the liquid. A batch method in which the process is repeated until the content of the alkali metal salt of the carboxylic acid is within the above range can be mentioned. Further, there is also a continuous method in which PVA is continuously added from the top of the tower at approximately the same temperature and for the same time as the batch method, and a cleaning liquid is continuously added from the bottom of the tower, and the two are brought into contact with each other.

The alkali metal salt of the carboxylic acid contained in the raw material PVA is obtained by neutralizing the alkali catalyst used in the saponification step, for example, sodium hydroxide, potassium hydroxide, sodium methylate, etc. with carboxylic acid, In addition, the carboxylic acid added for the purpose of suppressing alcoholysis of the vinyl ester monomer such as vinyl acetate used in the polymerization process is neutralized in the saponification process, to stop radical polymerization When a carboxylic acid having a conjugated double bond is used as an inhibitor to be added to the carboxylic acid, those obtained by neutralizing the carboxylic acid in the saponification step or those intentionally added are included. Specific examples include sodium acetate, potassium acetate, sodium propionate, potassium propionate, sodium glycerate, potassium glycerate, sodium malate, potassium malate, sodium citrate, potassium citrate, sodium lactate, potassium lactate, tartaric acid Sodium, potassium tartrate, sodium salicylate, potassium salicylate, sodium malonate, potassium malonate, sodium succinate, potassium succinate, sodium maleate, potassium maleate, sodium phthalate, potassium phthalate, sodium oxalate, potassium oxalate , Sodium glutarate, potassium glutarate, sodium abietic acid, potassium abietic acid, sodium sorbate, potassium sorbate, 2,4,6-octatri Sodium 1,1-carboxylate,

potassium

2,4,6-octatriene-1-carboxylate, sodium eleostearate, potassium eleostearate,

sodium

2,4,6,8-decatetraene-1-

carboxylate

2,4,6,8-decatetraene-1-carboxylate, sodium retinoate, potassium retinoate and the like, but are not limited thereto.

The PVA thus obtained is acetalized to produce polyvinyl acetal used for film production. Although the method of acetalization is not specifically limited, For example, the following method is mentioned. PVA is dissolved in water by heating to 80 to 100 ° C., and then gradually cooled over 10 to 60 minutes to obtain a 3 to 40% by mass aqueous solution of PVA. When the temperature falls to −10 to 30 ° C., an aldehyde and an acid catalyst are added to the aqueous solution, and an acetalization reaction is performed for 30 to 300 minutes while keeping the temperature constant. At that time, polyvinyl acetal having reached a certain degree of acetalization is precipitated. Thereafter, the temperature of the reaction solution is raised to 25 to 80 ° C. over 30 to 300 minutes, and the temperature is maintained for 10 minutes to 25 hours (this temperature is set as the reaction temperature for driving in). Next, a neutralizing agent such as an alkali is added to the reaction solution as necessary to neutralize the acid catalyst, and the resultant is washed with water and dried to obtain polyvinyl acetal.

In general, aggregated particles made of polyvinyl acetal are generated in such a reaction or processing step, and coarse particles are easily formed. When such coarse particles are generated, there is a risk of causing variation between batches. On the other hand, when PVA produced using a predetermined method to be described later is used as a raw material, the generation of coarse particles is suppressed as compared with the conventional product. As a result, when the obtained polyvinyl acetal is melt-cast, A film having a reduced dissolved content can be obtained.

The acid catalyst used in the acetalization reaction is not particularly limited, and any of organic acids and inorganic acids can be used. Examples thereof include acetic acid, paratoluenesulfonic acid, nitric acid, sulfuric acid, and hydrochloric acid. Of these, hydrochloric acid, sulfuric acid, and nitric acid are preferably used. In general, when nitric acid is used, the reaction rate of the acetalization reaction is increased, and improvement in productivity can be expected. On the other hand, the obtained polyvinyl acetal particles tend to be coarse and the variation between batches tends to increase. However, when the PVA of the present invention is used as a raw material, the formation of coarse particles is suppressed, and as a result, when the obtained polyvinyl acetal is melt-formed, a film with reduced foreign matter (undissolved content) is obtained. be able to.

The aldehyde used for the acetalization reaction of polyvinyl acetal is not particularly limited, but a conventionally known aldehyde having 1 to 8 carbon atoms is preferable, an aldehyde having 4 to 6 carbon atoms is more preferable, and n-butyraldehyde is particularly preferable. In the present invention, polyvinyl acetal obtained by using two or more aldehydes in combination can also be used.

In the present invention, as a method for adjusting each value obtained by GPC measurement of a multilayer film so as to fall within the above-mentioned range, 1) a method for forming a film by adding an antioxidant to polyvinyl acetal, 2) a predetermined method The method of using PVA manufactured using the method of (2) as a raw material of polyvinyl acetal (I) and polyvinyl acetal (II) is mentioned. You may combine these methods suitably.

The antioxidant used in the method 1) is not particularly limited, and examples thereof include phenolic antioxidants, phosphorus antioxidants, sulfur antioxidants, and the like. Among these, phenolic antioxidants are used. Preferably, alkyl-substituted phenolic antioxidants are particularly preferred.

Examples of phenolic antioxidants include 2-t-butyl-6- (3-t-butyl-2-hydroxy-5-methylbenzyl) -4-methylphenyl acrylate, 2,4-di-t-amyl- Acrylate compounds such as 6- (1- (3,5-di-t-amyl-2-hydroxyphenyl) ethyl) phenyl acrylate; 2,6-di-t-butyl-4-methylphenol, 2,6-di-t -Butyl-4-ethylphenol, octadecyl-3- (3,5-) di-t-butyl-4-hydroxyphenyl) propionate, 2,2'-methylene-bis (4-methyl-6-t-butylphenol), 4,4′-butylidene-bis (4-methyl-6-tert-butylphenol), 4,4′-butylidene-bis (6-tert-butyl-m-cresol), 4,4′-thiobi (3-methyl-6-tert-butylphenol), bis (3-cyclohexyl-2-hydroxy-5-methylphenyl) methane, 3,9-bis (2- (3- (3-tert-butyl-4-hydroxy) -5-methylphenyl) propionyloxy) -1,1-dimethylethyl) -2,4,8,10-tetraoxaspiro [5.5] undecane, 1,1,3-tris (2-methyl-4- Hydroxy-5-t-butylphenyl) butane, 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene, tetrakis (methylene-3- ( 3 ′, 5′-di-t-butyl-4′-hydroxyphenyl) propionate) methane, triethylene glycol bis (3- (3-t-butyl-4-hydroxy-5-methylphenyl) Alkyl-substituted phenolic compounds such as propionate); 6- (4-hydroxy-3,5-di-t-butylanilino) -2,4-bis-octylthio-1,3,5-triazine, 6- (4-hydroxy-) 3,5-dimethylanilino) -2,4-bis-octylthio-1,3,5-triazine, 6- (4-hydroxy-3-methyl-5-t-butylanilino) -2,4-bis-octylthio Triazine group-containing phenolic compounds such as 1,3,5-triazine, 2-octylthio-4,6-bis- (3,5-di-t-butyl-4-oxyanilino) -1,3,5-triazine There is.

Examples of phosphorus antioxidants include triphenyl phosphite, diphenylisodecyl phosphite, phenyl diisodecyl phosphite, tris (nonylphenyl) phosphite, tris (dinonylphenyl) phosphite, tris (2-t-butyl). -4-methylphenyl) phosphite, tris (cyclohexylphenyl) phosphite, 2,2-methylenebis (4,6-dit-butylphenyl) octyl phosphite, 9,10-dihydro-9-oxa-10-phos Phaphenanthrene-10-oxide, 10- (3,5-di-t-butyl-4-hydroxybenzyl) -9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, 10-decyloxy-9 , 10-Dihydro-9-oxa-10-phospha Monophosphite compounds such as enanthrene; 4,4′-butylidene-bis (3-methyl-6-tert-butylphenyl-ditridecyl phosphite), 4,4′-isopropylidene-bis (phenyl-dialkyl (C12 To C15) phosphite), 4,4′-isopropylidene-bis (diphenylmonoalkyl (C12 to C15) phosphite), 1,1,3-tris (2-methyl-4-ditridecyl phosphite-5- and diphosphite compounds such as t-butylphenyl) butane and tetrakis (2,4-di-t-butylphenyl) -4,4′-biphenylene phosphite. Of these, monophosphite compounds are preferred.

Examples of the sulfur-based antioxidant include dilauryl 3,3′-thiodipropionate, distearyl 3,3′-thiodipropionate, lauryl stearyl 3,3′-thiodipropionate, pentaerythritol-tetrakis- (Β-lauryl-thiopropionate), 3,9-bis (2-dodecylthioethyl) -2,4,8,10-tetraoxaspiro [5.5] undecane.

These antioxidants can be used alone or in combination of two or more. The blending amount of the antioxidant is not particularly limited, but is 0.001 to 5 parts by mass, preferably 0.01 to 1 part by mass with respect to 100 parts by mass of the polyvinyl acetal. When the amount of the antioxidant is less than 0.001 part by mass, a sufficient effect may not be exhibited, and when it exceeds 5 parts by mass, the effect cannot be improved by increasing the blending amount.

The following A) to H) are mentioned as a method for producing PVA used in the above method 2).

A) A vinyl ester monomer from which a radical polymerization inhibitor contained in the raw material vinyl ester monomer has been removed in advance is used for polymerization.

B) A vinyl ester monomer having a total content of impurities contained in the raw material vinyl ester monomer of preferably 1 to 1200 ppm, more preferably 3 to 1100 ppm, and even more preferably 5 to 1000 ppm is used for radical polymerization. Impurities include aldehydes such as acetaldehyde, crotonaldehyde, and acrolein; acetals such as acetaldehyde dimethyl acetal, crotonaldehyde dimethyl acetal, and acrolein dimethyl acetal obtained by acetalizing the aldehyde with a solvent alcohol; ketones such as acetone; methyl acetate and ethyl acetate And esters.

C) In order to suppress the alcoholysis and hydrolysis of the monomer by alcohol and a small amount of water in a series of steps of radical polymerization of the raw material vinyl ester monomer in an alcohol solvent and collecting and reusing unreacted monomer, Organic acids, specifically hydroxycarboxylic acids such as glycolic acid, glyceric acid, malic acid, citric acid, lactic acid, tartaric acid, salicylic acid; malonic acid, succinic acid, maleic acid, phthalic acid, oxalic acid, glutaric acid, etc. A carboxylic acid or the like is added to suppress the generation of aldehydes such as acetaldehyde generated by decomposition as much as possible. The addition amount of the organic acid is preferably 1 to 500 ppm, more preferably 3 to 300 ppm, and still more preferably 5 to 100 ppm with respect to the raw material vinyl ester monomer.

D) As the solvent used for the polymerization, a solvent having a total impurity content of preferably 1 to 1200 ppm, more preferably 3 to 1100 ppm, and still more preferably 5 to 1000 ppm. Examples of the impurities contained in the solvent include those described above as the impurities contained in the raw material vinyl ester monomer.

E) When the radical polymerization of the vinyl ester monomer, the ratio of the solvent to the vinyl ester monomer is increased.

F) An organic peroxide is used as a radical polymerization initiator used for radical polymerization of a vinyl ester monomer. Organic peroxides include acetyl peroxide, isobutyl peroxide, diisopropyl peroxycarbonate, diallyl peroxydicarbonate, di-n-propyl peroxydicarbonate, dimyristyl peroxydicarbonate, di (2-ethoxyethyl) peroxide Examples include oxydicarbonate, di (2-ethylhexyl) peroxydicarbonate, di (methoxyisopropyl) peroxydicarbonate, and di (4-tert-butylcyclohexyl) peroxydicarbonate. It is preferable to use peroxydicarbonate with a period of 10 to 110 minutes.

G) When an inhibitor is added after radical polymerization of the vinyl ester monomer in order to suppress the polymerization, an inhibitor of 5 molar equivalents or less is added to the remaining undecomposed radical polymerization initiator. Examples of the inhibitor include a compound having a conjugated double bond having a molecular weight of 1000 or less and a compound that stabilizes a radical and inhibits a polymerization reaction. Specifically, isoprene, 2,3-dimethyl-1,3-butadiene, 2,3-diethyl-1,3-butadiene, 2-t-butyl-1,3-butadiene, 1,3-pentadiene, , 3-dimethyl-1,3-pentadiene, 2,4-dimethyl-1,3-pentadiene, 3,4-dimethyl-1,3-pentadiene, 3-ethyl-1,3-pentadiene, 2-methyl-1 , 3-pentadiene, 3-methyl-1,3-pentadiene, 4-methyl-1,3-pentadiene, 1,3-hexadiene, 2,4-hexadiene, 2,5-dimethyl-2,4-hexadiene, , 3-octadiene, 1,3-cyclopentadiene, 1,3-cyclohexadiene, 1-methoxy-1,3-butadiene, 2-methoxy-1,3-butadiene, 1-ethoxy-1,3- Tadiene, 2-ethoxy-1,3-butadiene, 2-nitro-1,3-butadiene, chloroprene, 1-chloro-1,3-butadiene, 1-bromo-1,3-butadiene, 2-bromo-1, Conjugated dienes comprising a conjugated structure of two carbon-carbon double bonds such as 3-butadiene, fulvene, tropone, osymene, ferrandrene, myrcene, farnesene, semblene, sorbic acid, sorbic acid ester, sorbic acid salt, abietic acid; Conjugated triene having a conjugated structure of three carbon-carbon double bonds such as 1,3,5-hexatriene, 2,4,6-octatriene-1-carboxylic acid, eleostearic acid, tung oil, cholecalciferol Carbons such as cyclooctatetraene, 2,4,6,8-decatetraene-1-carboxylic acid, retinol, retinoic acid, etc. Polyenes such as conjugated polyene consisting Motoni double bond of four or more conjugated structure. Any one having a plurality of stereoisomers such as 1,3-pentadiene, myrcene, and farnesene may be used. Further, p-benzoquinone, hydroquinone, hydroquinone monomethyl ether, 2-phenyl-1-propene, 2-phenyl-1-butene, 2,4-diphenyl-4-methyl-1-pentene, 3,5-diphenyl-5 Methyl-2-heptene, 2,4,6-triphenyl-4,6-dimethyl-1-heptene, 3,5,7-triphenyl-5-ethyl-7-methyl-2-nonene, 1,3- Diphenyl-1-butene, 2,4-diphenyl-4-methyl-2-pentene, 3,5-diphenyl-5-methyl-3-heptene, 1,3,5-triphenyl-1-hexene, 2,4 , 6-triphenyl-4,6-dimethyl-2-heptene, 3,5,7-triphenyl-5-ethyl-7-methyl-3-nonene, 1-phenyl-1,3-butadiene, 1,4 -The Aromatic compounds such as Eniru 1,3-butadiene.

H) A polyvinyl ester alcohol solution from which the remaining vinyl ester monomer is removed as much as possible is used for the saponification reaction. Preferably, the residual monomer removal rate is 99% or more, more preferably 99.5% or more, still more preferably 99.8% or more.

The desired PVA can be obtained by appropriately combining A) to H). PVA thus obtained is preferably used as a raw material for polyvinyl acetal (I) and polyvinyl acetal (II).

The plasticizer contained in the layer (X) and the layer (Y) is not particularly limited as long as the effect of the present invention is not impaired and there is no problem in compatibility with polyvinyl acetal. The plasticizers can be used alone or in combination of two or more. The plasticizer is preferably a diester of an oligoalkylene glycol having a hydroxyl group at both ends and an aliphatic carboxylic acid, or a diester of an alkylene dicarboxylic acid and an aliphatic monohydric alcohol. Examples of oligoalkylene glycols having hydroxyl groups at both ends include ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,2-propylene glycol, 1,2-propylene glycol dimer and trimer, 1,3 -Propylene glycol, 1,3-propylene glycol dimer and trimer, 1,2-butylene glycol, 1,2-butylene glycol dimer and trimer, 1,4-butylene glycol, 1, 4-butylene glycol dimer and trimer, 1,2-hexanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,2-octanediol, 1,8-octane Diol, 1,9-nonanediol, 2-methyl-1,8-octanediol, , 2-decanediol, 1,4-cyclohexane diol. Examples of the aliphatic carboxylic acid include acetic acid, propanoic acid, butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, 2-ethylhexanoic acid, nonanoic acid, decanoic acid and the like. Here, the combination of oligoalkylene glycol and aliphatic carboxylic acid is arbitrary, and may be a combination of a plurality of oligoalkylene glycols and a plurality of carboxylic acids. Among these, a diester of triethylene glycol and 2-ethylhexanoic acid is preferable from the viewpoint of handleability (volatility during molding). Triethylene glycol-di-2-ethylhexanoate is particularly preferable. Examples of the alkylene dicarboxylic acid include oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, and sebacic acid. Aliphatic monohydric alcohols include methanol, ethanol, propanol, butanol, pentanol, hexanol, cyclohexanol, heptanol, octanol, 2-ethylhexanol, nonaol, decanol, 2-methoxyethanol, 2-ethoxyethanol, 2-propoxy Examples include ethanol and 2-butoxyethanol. Here, the combination of an alkylene dicarboxylic acid and an aliphatic monohydric alcohol is arbitrary, and a combination of a plurality of alkylene dicarboxylic acids and a plurality of aliphatic monohydric alcohols may be used.

As the plasticizer, an aliphatic compound having a hydroxyl group such as an aliphatic ester compound having a hydroxyl group or an aliphatic ether compound having a hydroxyl group may be used. The number of hydroxyl groups in these compounds is preferably 2 or more, more preferably 2 to 3. The aliphatic ester compound having a hydroxyl group is a compound having at least one ester bond and having a hydroxyl group, and the aliphatic ether compound having a hydroxyl group is a compound having at least one ether bond and having a hydroxyl group. .

The aliphatic ester compound having a hydroxyl group is not particularly limited, but methyl ricinoleate, butyl ricinoleate, 2-ethylhexyl ricinoleate, ricinoleic acid (2-hydroxyethyl), glycerin monoricinoleate, glycerin diricinoleate, glycerin triglyceride. Ricinoleic acid ester, glycerin diricinoleic acid monooleate, oleic acid (2-hydroxyethyl), 2-ethylhexanoic acid (2-hydroxyethyl), ricinoleic acid {2- [2- (2-hydroxyethoxy) ethoxy ] Ethyl} 2-ethylhexanoic acid {2- [2- (2-hydroxyethoxy) ethoxy] ethyl}, methyl ricinoleate, ethyl ricinoleate, butyl ricinoleate, octyl ricinoleate, 6-hydroxyhexanoic acid Chill, 12-hydroxystearic acid methyl other such castor, and polyester compounds having a hydroxyl group. Castor oil is a glycerin tricarboxylic acid ester obtained from castor seeds, and most of the carboxylic acid ester portion, usually 80 to 95% by mass, is ricinoleic acid ester, and the remainder is palmitic acid ester, stearic acid ester, It is composed of oleic acid ester, linoleic acid ester, linolenic acid ester and the like.

Examples of the polyester compound having a hydroxyl group include an aliphatic polyester having a hydroxyl group, which is a condensation copolymer of a polyvalent carboxylic acid and a polyhydric alcohol, an aliphatic polyester having a hydroxyl group, which is a polymer of a hydroxycarboxylic acid, and a hydroxyl group. Aliphatic polycarbonate polyol having

An aliphatic polyester having a hydroxyl group, which is a condensation copolymer of a polycarboxylic acid and a polyhydric alcohol, can be obtained by condensation polymerization of an aliphatic polycarboxylic acid and an aliphatic polyhydric alcohol in an excess of polyhydric alcohol. .

Examples of aliphatic polycarboxylic acids include succinic acid, glutaric acid, adipic acid, suberic acid, sebacic acid, dodecanedioic acid, 1,2-cyclohexanedicarboxylic acid, and other aliphatic divalent carboxylic acids, 1,2,3-propane Examples thereof include, but are not limited to, tricarboxylic acids and aliphatic trivalent carboxylic acids such as 1,3,5-pentatricarboxylic acid. Of these, aliphatic divalent carboxylic acids, particularly aliphatic divalent carboxylic acids having 6 to 10 carbon atoms are preferred. Examples of the aliphatic polyhydric alcohol include 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, and 1,2-hexane. Diol, 3-methyl-1,5-pentanediol, 1,2-octanediol, 1,2-nonanediol, 1,8-nonanediol, 1,9-nonanediol, 1,2-cyclohexanediol, 1, Examples include aliphatic dihydric alcohols such as 2-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, diethylene glycol and triethylene glycol; aliphatic trihydric alcohols such as glycerin; aliphatic tetrahydric alcohols such as erythritol and pentaerythritol. However, it is not limited to these. Of these, aliphatic dihydric alcohols are preferred from the viewpoint of excellent weather resistance of the resulting polyester.

An aliphatic polyester having a hydroxyl group, which is a polymer of hydroxycarboxylic acid, can be obtained by condensation polymerization of hydroxycarboxylic acid. Examples of the hydroxycarboxylic acid include glycolic acid, lactic acid, 2-hydroxybutanoic acid, 3-hydroxybutanoic acid, 4-hydroxybutanoic acid, 6-hydroxyhexanoic acid, ricinoleic acid and the like. A lactone compound obtained by intramolecular condensation of these hydroxycarboxylic acids can also be used as a raw material. Examples of the lactone compound include, but are not limited to, β-butyrolactone, δ-valerolactone, ε-caprolactone, 4-methyl-δ-valerolactone, and the like. When a lactone compound is used, a polyester can be obtained by ring-opening polymerization. Of these, 6-hydroxycarboxylic acid or ε-caprolactone is preferred from the viewpoint of excellent heat resistance of the polyester.

Examples of the aliphatic ether compound having a hydroxyl group include ethylene glycol monohexyl ether and an aliphatic polyether compound having a hydroxyl group. Among these, an aliphatic polyether compound having a hydroxyl group is preferable. The aliphatic polyether compound having a hydroxyl group is a polymer of an aliphatic polyhydric alcohol such as ethylene glycol and 1,2-propylene glycol and having a hydroxyl group. For example, polyethylene glycol and polypropylene glycol are preferable.

The molecular weight of the aliphatic compound having a hydroxyl group is not particularly limited, but is preferably 200 to 2000, more preferably 220 to 1000, and still more preferably 250 to 700. The number average molecular weight based on the hydroxyl value of the compound is not particularly limited, but is preferably 200 to 2000, more preferably 220 to 1700, and further preferably 240 to 1500. When the number average molecular weight based on the hydroxyl value is smaller than 200, the boiling point of the compound may not be sufficiently high, and high volatility may be a problem. When the number average molecular weight based on the hydroxyl value is larger than 2000, the compatibility between the compound and polyvinyl acetal may be insufficient. The number average molecular weight based on the hydroxyl value is (number of hydroxyl groups per molecule having a hydroxyl group) / (substance amount of hydroxyl group per 1 g of the compound having a hydroxyl group [mol / g]) = 1000 × (compound having a hydroxyl group) This is a value obtained by (number of hydroxyl groups per molecule) / ((hydroxyl value of a compound having a hydroxyl group) / 56). Here, when two or more types of aliphatic compounds having a hydroxyl group are used as a mixture, the number of hydroxyl groups per molecule of a compound having a hydroxyl group indicates an average value per molecule of the compound having a hydroxyl group contained in the mixture. .

The hydroxyl value of the aliphatic compound having a hydroxyl group is not particularly limited, but is preferably 50 to 600 mgKOH / g, more preferably 70 to 500 mgKOH / g, and further preferably 100 to 400 mgKOH / g. If the hydroxyl value is less than 50 mgKOH / g, the transparency of the resulting multilayer film may be reduced. On the other hand, when the hydroxyl value exceeds 600 mgKOH / g, the compatibility with polyvinyl acetal is lowered, transparency may be lowered, and bleeding may occur from the multilayer film. Here, the hydroxyl value in the present invention is a value obtained by measurement by the method described in JIS K1557-1 (2007). The hydroxyl value in the case of using a mixture of two or more compounds having a hydroxyl group is a mixture thereof (mixture of compounds having a hydroxyl group having the same mixing ratio as the mixing ratio of the plasticizer in each layer of the multilayer film of the present invention). Of hydroxyl value.

As a plasticizer contained in the layer (X) and the layer (Y), a compound having an aromatic ring such as an ether compound of a polyalkylene glycol and an aromatic alcohol or an ester compound of a polyalkylene glycol and an aromatic carboxylic acid is used. You can also. The molecular weight of the compound is not particularly limited, but is preferably 200 to 2000, more preferably 220 to 1500, and still more preferably 250 to 1000.

Specific examples of ether compounds of polyalkylene glycol and aromatic alcohol include polyoxyethylene phenyl ether, polyoxyethylene methyl phenyl ether, polyoxyethylene ethyl phenyl ether, polyoxyethylene n-propyl phenyl ether, polyoxyethylene i. Polyoxyethylene alkylphenyl ethers such as -propylphenyl ether, polyoxyethylene i-propylmethylphenyl ether, polyoxyethylene n-butylphenyl ether, polyoxyethylene i-butylphenyl ether, polyoxyethylene t-butylphenyl ether Can be mentioned. The polyoxyethylene alkylphenyl ether is preferably a monoether. It is also preferable that the alkyl group on the aromatic ring of the polyoxyethylene alkylphenyl ether has 4 or less carbon atoms.

Further, as an ether compound of polyalkylene glycol and aromatic alcohol, aromatic alcohol having a plurality of aromatic rings such as polyoxyethylene monobenzyl phenyl ether, polyoxyethylene dibenzyl phenyl ether, polyoxyethylene tribenzyl phenyl ether and polyoxyethylene monobenzyl phenyl ether Also included are ether compounds with alkylene glycols. Moreover, the ether compound of aromatic alcohol and polyalkylene glycol which have condensed aromatic rings, such as polyoxyethylene naphthyl ether, is also mentioned. These ether compounds are preferably monoethers. Furthermore, a compound etherified with a plurality of polyethylene glycols such as 2,2-bis (4-polyoxyethyleneoxyphenyl) propane may be mentioned.

Specific examples of ester compounds of polyalkylene glycols and aromatic carboxylic acids include esters of aromatic carboxylic acids such as benzoic acid, phthalic acid, isophthalic acid, terephthalic acid, and trimellitic acid with polyalkylene glycols such as polyethylene glycol. Compounds.

Among the compounds having an aromatic ring described above, polyoxyethylene alkylphenyl ether, an ether compound of an aromatic alcohol having a plurality of aromatic rings and polyoxyethylene, and an ether of an aromatic alcohol having a condensed aromatic ring and a polyalkylene glycol Compounds are preferred, more preferably they are monoethers.

The solubility of the plasticizer used in the present invention in water is not particularly limited, but the amount of dissolution in 100 g of water at 20 ° C. is preferably 100 g or less. When the amount of the plasticizer dissolved is in such a range, it is preferable that when the resulting multilayer film comes into contact with water, the plasticizer is less likely to be eluted by water. The amount of the plasticizer dissolved in 100 g of water at 20 ° C. is more preferably 50 g or less, further preferably 10 g or less, and particularly preferably 2 g or less.

The content of the plasticizer in the multilayer film of the present invention is preferably 20 to 100 parts by mass with respect to 100 parts by mass of polyvinyl acetal (I) or polyvinyl acetal (II) for each layer. If it is less than 20 mass parts, the impact resistance of the laminated glass or the laminated glass using the multilayer film as an intermediate film may be insufficient. On the other hand, when the amount exceeds 100 parts by mass, the plasticizer may bleed out and the transparency of the resulting multilayer film may be reduced, or the adhesion to glass may be impaired.

Further, the difference between the plasticizer content relative to 100 parts by mass of the polyvinyl acetal (II) in the layer (Y) and the plasticizer content relative to 100 parts by mass of the polyvinyl acetal (I) in the layer (X) is 5 parts by mass or more. It is preferable from the viewpoint of sound insulation performance. The content difference is preferably 7.5 parts by mass or more, and more preferably 10 parts by mass or more. The difference in content is preferably 50 parts by mass or less.

Layer (X) contains an ultraviolet absorber. The layer (X) located outside the layer (Y) containing the heat ray shielding fine particles contains an ultraviolet absorber, thereby preventing the heat ray shielding fine particles from being exposed to ultraviolet rays, and causing deterioration of the resin and particles caused by the photocatalytic activity of the particles. Can be prevented. Moreover, the ultraviolet absorber may also be contained in the layer (Y).

The ultraviolet absorber contained in the layer (X) is not particularly limited, but 2- (5-methyl-2-hydroxyphenyl) benzotriazole, 2- (2-hydroxy-3,5-bis ( α, α'dimethylbenzyl) phenyl) -2H-benzotriazole, 2- (3,5-di-t-butyl-2-hydroxyphenyl) benzotriazole, 2- (3-t-butyl-5-methyl-2- Hydroxyphenyl) -5-chlorobenzotriazole, 2- (3,5-di-t-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole, 2- (3,5-di-t-amyl- Benzotriazole UV absorption such as 2-hydroxyphenyl) benzotriazole, 2- (2′-hydroxy-5′-t-octylphenyl) benzotriazole Agent: 2,2,6,6-tetramethyl-4-piperidylbenzoate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1,2,2,6,6-pentamethyl) -4-piperidyl) -2- (3,5-di-t-butyl-4-hydroxybenzyl) -2-n-butyl malonate, 4- (3- (3,5-di-t-butyl-4-hydroxy) Hindered amines such as phenyl) propionyloxy) -1- (2- (3- (3,5-di-t-butyl-4-hydroxyphenyl) propionyloxy) ethyl) -2,2,6,6-tetramethylpiperidine UV absorber; benzo such as 2,4-di-t-butylphenyl-3,5-di-t-butyl-4-hydroxybenzoate, hexadecyl-3,5-di-t-butyl-4-hydroxybenzoate UV absorbers; malonic acid ester UV absorbers such as malonic acid [(4-methoxyphenyl) -methylene] -dimethyl ester, and oxalic acid anilides such as 2-ethyl-2'-ethoxy-oxalanilide Examples include ultraviolet absorbers. Examples of commercially available ultraviolet absorbers include benzotriazole ultraviolet absorbers such as Tinuvin P, Tinuvin 213, Tinuvin 234, Tinuvin 326, Tinuvin 328, Tinuvin 329, and Tinuvin 571 manufactured by Ciba Japan, and triazine ultraviolet absorbers such as Tinuvin 1577 manufactured by Ciba Japan. Examples thereof include benzophenone-based ultraviolet absorbers such as CHIMASSORB 81 manufactured by Ciba Japan, and malonate-based ultraviolet absorbers such as Hostavin PR-25 manufactured by Clariant. These ultraviolet absorbers can be used alone or in combination of two or more. In addition, a known light stabilizer such as a hindered amine compound may be used in combination.

The content of the ultraviolet absorber in the layer (X) is not particularly limited, but is preferably 0.01 to 5 parts by mass with respect to 100 parts by mass of the total amount of polyvinyl acetal (I) and plasticizer. When the addition amount is less than 0.01 parts by mass, a sufficient ultraviolet shielding effect may not be expected. More preferably, it is 0.05 mass part or more, More preferably, it is 0.1 mass part or more. Moreover, when the addition amount exceeds 5 parts by mass, the coloring of the multilayer film may be remarkably unsuitable. More preferably, it is 2 mass parts or less, More preferably, it is 1 mass part or less.

The glass transition temperature of the resin composition containing the polyvinyl acetal (I) constituting the layer (X), the ultraviolet absorber, and the plasticizer is not particularly limited and may be appropriately selected depending on the intended purpose. Preferably, the temperature is in the range of 5 to 45 ° C, more preferably 10 to 40 ° C. When the multilayer film of the present invention is used as a laminated glass interlayer, the glass transition temperature is preferably in the above range.

The layer (Y) contains heat ray shielding fine particles for the purpose of imparting heat ray shielding properties. The heat ray shielding fine particles used in this case are not particularly limited as long as they have a property of absorbing at least light in the near-infrared wavelength region as a function. For example, tin-doped indium oxide, antimony-doped tin oxide, aluminum-doped oxidation Examples thereof include zinc, indium-doped zinc oxide, gallium-doped zinc oxide, tungsten oxide, lanthanum hexaboride, cerium hexaboride, anhydrous zinc antimonate, and copper sulfide. These may be used alone or in combination of two or more. Among these, it is preferable to contain anhydrous zinc antimonate from the viewpoints of performance, safety, raw material availability, price, and the like. The heat ray shielding fine particles may be contained in the layer (X) as necessary.

The heat ray shielding fine particles are preferably contained in an amount of 0.001 to 5 parts by mass with respect to 100 parts by mass of the total amount of polyvinyl acetal (II) and plasticizer in the layer (Y). If the content is less than 0.001 part by mass, the expected heat ray shielding effect may not be obtained. More preferably, it is 0.002 mass part or more, More preferably, it is 0.005 mass part or more. Moreover, when content exceeds 5 mass parts, there exists a possibility that the transparency of a multilayer film may be impaired. More preferably, it is 2 parts by mass or less.

The layer (Y) contains a surfactant as a dispersant for the heat ray shielding fine particles. When the surfactant is adsorbed on the surface of the heat ray shielding fine particles, the surface is hydrophobized, and aggregation of particles generated when combined with polyvinyl acetal (II) or a plasticizer can be effectively suppressed.

The surfactant is not particularly limited as long as it is not contrary to the gist of the present invention, but a phosphate ester is preferable. The phosphate ester is not particularly limited, and a phosphate ester of a monobasic acid or a dibasic acid is preferably used. For example, Disperbyk-102, Disperbyk-103, Disperbyk-106, Disperbyk-107, Disperbyk-108, Disperbyk-110, Disperbyk-111, Disperbyk-182D, Disperbyk-182 185, Disperbyk-187, Disperbyk-190, Disperbyk-191, Disperbyk-192, Daiichi Kogyo Seiyaku Co., Ltd., PRISURF A208B, PRISURF A210B, PRISURF A212C, PRISURF A213B, PRISURF A215C, PRISURF A215C A212C, Price Surf 219B, Prisurf AL, Prisurf M208F, Adeka Coal TS-230E, Adeka Coal CS-141E, Adeka Coal CS-1361E, Adeka Coal CS-279, Adeka Coal PS-440E, Adeka Coal PS-810E, Adeka Coal PS-807, Adeka Coal PS -984 or the like. These may be used alone or in combination of two or more.

The content of the surfactant in the layer (Y) is preferably 0.005 to 2 parts by mass with respect to 100 parts by mass of the total amount of the polyvinyl acetal (II) and the plasticizer in the layer (Y). . If the content is less than 0.005 parts by mass, the dispersion effect may not be sufficiently obtained. More preferably, it is 0.05 mass part or more, More preferably, it is 0.1 mass part or more. Moreover, when it exceeds 2 mass parts, the bleed-out of surfactant will be remarkable and the adhesive force with respect to glass may not be hold | maintained stably. More preferably, it is 1.8 parts by mass or less.

In the multilayer film of the present invention, the layer (Y) is likely to deteriorate due to the influence of the heat-shielding fine particles and the surfactant. Add salt.

The alkali metal salt and / or alkaline earth metal salt is not particularly limited, and examples of the alkali metal and / or alkaline earth metal forming the salt include sodium, potassium, magnesium and the like. Examples of the acid forming the salt include linear carboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, hexanoic acid and octanoic acid, and branched carboxylic acids such as 2-ethylbutanoic acid and 2-ethylhexanoic acid. Examples thereof include organic acids such as acids, and inorganic acids such as hydrochloric acid, nitric acid, and sulfuric acid. These may be used alone or in combination of two or more.

The content of the alkali metal salt and / or alkaline earth metal salt in the layer (Y) is the total content of the alkali metal and / or alkaline earth metal derived from the alkali metal salt and / or alkaline earth metal salt. Is preferably 0.006 to 0.2 parts by mass with respect to 100 parts by mass of polyvinyl acetal (II). If it is less than 0.006 parts by mass, deterioration of the resin derived from the surfactant may not be sufficiently suppressed. More preferably, it is 0.008 mass part or more. Moreover, when content exceeds 0.2 mass part, aggregation of a heat ray shielding fine particle will be accelerated | stimulated and the transparency of the multilayer film obtained as a result may be lost. More preferably, it is 0.1 mass part or less.

The glass transition temperature of the resin composition containing polyvinyl acetal (II) constituting the layer (Y), heat ray shielding fine particles, surfactant, alkali metal salt and / or alkaline earth metal salt, and plasticizer is not particularly limited. The temperature can be appropriately selected depending on the purpose, but is preferably in the range of 0 to 45 ° C, more preferably 0 to 35 ° C, and further preferably 0 to 30 ° C. When the multilayer film of the present invention is used as a laminated glass interlayer, the glass transition temperature is preferably in the above range.

Layer (X) and layer (Y), unless contrary to the gist of the present invention, adhesion improver, pigment, dye, stabilizer, lubricant, flame retardant, processing aid, antistatic agent, colorant, impact resistance Auxiliaries, fillers, moisture-proofing agents, and other conventionally known additives may be included.

The method for obtaining the layer (X) constituting the multilayer film of the present invention is not particularly limited; after forming a film obtained by dissolving or dispersing polyvinyl acetal (I), an ultraviolet absorber and a plasticizer in an organic solvent, Examples include a method of distilling off the organic solvent; a method of melt-molding a resin composition containing polyvinyl acetal (I), an ultraviolet absorber and a plasticizer. Among these, the latter is preferable from the viewpoint of productivity and the like.

When the layer (X) is obtained by the melt molding method, the method of adding the ultraviolet absorber is not particularly limited, but it is added to the polyvinyl acetal (I) in a state where the ultraviolet absorber is dissolved or suspended in advance in a plasticizer. It is preferable. Moreover, there is no restriction | limiting in particular as a method of mixing a raw material, However, Mixing by melt-kneading is preferable from viewpoints of productivity. The melt kneading method is not particularly limited, and a known kneader such as a single screw extruder, a twin screw extruder, a brabender, an open roll, or a kneader can be used. The resin temperature at the time of melt kneading is preferably 150 to 250 ° C, more preferably 170 to 230 ° C. If the resin temperature becomes too high, the polyvinyl acetal (I) will be decomposed, and the content of volatile substances in the film after film formation will increase. On the other hand, if the temperature is too low, volatile matter removal by the kneader becomes insufficient, and the content of volatile substances in the film after film formation increases. In order to efficiently remove the volatile substance, it is preferable to remove the volatile substance from the vent port by reducing the pressure in the kneader.

The mixed melt is melt-molded into a film. A known method can be adopted as the molding method. A film can be produced by directly attaching a T-die to the melt-kneading apparatus, or a resin composition pellet can be produced once, and then a film can be separately formed.

The method for obtaining the layer (Y) constituting the multilayer film of the present invention is not particularly limited; polyvinyl acetal (II), heat ray shielding fine particles, surfactant, alkali metal salt and / or alkaline earth metal salt, and plastic A method in which an organic solvent is dissolved or dispersed in an organic solvent, and then the organic solvent is distilled off; polyvinyl acetal (II), heat ray shielding fine particles, surfactant, alkali metal salt and / or alkaline earth metal Examples thereof include a method of melt-molding a resin composition containing a salt and a plasticizer. Among these, the latter is preferable from the viewpoint of productivity and the like. The melt molding method preferably includes a step of melt-kneading a dispersion of a heat ray shielding fine particle and a plasticizer with respect to polyvinyl acetal (II) and forming the film into a film shape. More preferably, the metal salt and / or alkaline earth metal salt are mixed separately and then melt-molded. By mixing separately, aggregation of heat ray shielding fine particles is suppressed, and as a result, a film having a further lower haze can be obtained.

As a method of separately mixing heat ray shielding fine particles and alkali metal salt and / or alkaline earth metal salt with respect to polyvinyl acetal (II), for example; shielding fine particles, alkali metal salt and / or alkaline earth A method of separately adding a metal salt to the polyvinyl acetal (II) as it is; a dispersion of heat ray shielding fine particles and an alkali metal salt and / or an alkaline earth metal salt separately from the polyvinyl acetal (II) A method of mixing alkali metal salt and / or alkaline earth metal salt solution and heat ray shielding fine particles separately into polyvinyl acetal (II); a dispersion of heat ray shielding fine particles, an alkali metal salt and / Or a method of separately mixing alkaline earth metal salt solution with polyvinyl acetal (II); A method of mixing a molded article of polyvinyl acetal (II) and a solution of an alkali metal salt and / or an alkaline earth metal salt; a molded article of polyvinyl acetal containing an alkali metal salt and / or an alkaline earth metal salt; Examples thereof include a method of mixing with a dispersion of heat ray shielding fine particles. Among these, as described above, a method of mixing the heat ray shielding fine particles as a dispersion is preferable, and the dispersion of the heat ray shielding fine particles and the alkali metal salt and / or alkaline earth metal salt solution are separately obtained from polyvinyl acetal ( The method of mixing in II) is more preferred.

The surfactant may be added to any one of the dispersion of the heat ray shielding fine particles and the alkali metal salt and / or alkaline earth metal salt solution. From the viewpoint of the dispersibility of the heat ray shielding fine particles, at least heat rays are added. It is preferably contained in a dispersion of shielding fine particles. As a method for obtaining a dispersion of heat ray shielding fine particles containing a surfactant, a method of mixing heat ray shielding fine particles, a surfactant and a solvent followed by pulverization treatment, including heat ray shielding fine particles and a solvent, pulverization treatment was performed. Either a method of adding a surfactant to the dispersion, or a method of adding a dispersion containing heat ray shielding fine particles and a solvent and subjected to pulverization treatment to the surfactant may be used. Further, the order of mixing the dispersion of the heat ray shielding fine particles, the alkali metal salt and / or alkaline earth metal salt solution, the plasticizer and the polyvinyl acetal (II) is not particularly limited.

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

Further, the solvent contained in the alkali metal salt and / or alkaline earth metal salt solution is not particularly limited, and a solvent similar to the dispersion of the heat ray shielding fine particles can be used as the solution. An aqueous solution of an alkali metal salt and / or alkaline earth metal salt suspended in a plasticizer can also be added.

In obtaining the layer (Y), the method of mixing the raw materials is not particularly limited, but it is preferable to mix by melt kneading from the viewpoint of productivity and the like. The method of melt kneading is not particularly limited, and the above-described kneader used for melt kneading the raw material of the layer (X) is used.

The mixed melt is melt-molded into a film. As the forming method, the method described above as the melt forming method used for the production of the layer (X) is used.

As a method for producing a multilayer film, a general molding method can be applied. That is, a method in which the resin composition of each layer is coextruded to a die or a feed block, a method in which each layer is separately formed into a film, and then bonded together are included.

The thickness of the layer (X) constituting the multilayer film of the present invention is not particularly limited. The thickness of the layer (X) is preferably 0.05 to 1.2 mm, more preferably 0.07 to 1 mm, and further preferably 0.1 to 0.7 mm. If the thickness is less than 0.05 mm, the mechanical strength of the multilayer film may be reduced, and if it exceeds 1.2 mm, the flexibility of the multilayer film may be insufficient. Therefore, when the thickness of the layer (X) deviates from 0.05 to 1.2 mm, the laminated film obtained when the multilayer film of the present invention is used as an interlayer film of laminated glass. The safety of the glass may be reduced.

The thickness of the layer (Y) constituting the multilayer film of the present invention is not particularly limited. The thickness of the layer (Y) is preferably from 0.01 to 1 mm, more preferably from 0.02 to 0.8 mm, still more preferably from 0.05 to 0.5 mm. When the thickness is less than 0.01 mm, the sound insulation performance of the laminated glass using the multilayer film of the present invention as an interlayer film of the laminated glass may be deteriorated. When the thickness exceeds 1 mm, the mechanical strength of the multilayer film cannot be expected by increasing the thickness.

Further, the ratio (Y / X) of the thickness of the layer (Y) to the thickness of the layer (X) is not particularly limited, but is preferably 0.05 to 4 from the viewpoint of the mechanical strength and the sound insulation, and 0.07 To 2 is more preferable, and 0.1 to 0.8 is more preferable.

The multilayer film of the present invention has layers (X) arranged on both outer sides of the layer (Y). That is, any of the outermost layers is the layer (X). In particular, when the multilayer film of the present invention is used as an interlayer film for laminated glass, if both outermost layers are layers (X), the adhesiveness between the multilayer film and the glass can be adjusted appropriately. The merit of such a layer structure is great. Examples of the layer configuration include layer (X) / layer (Y) / layer (X), layer (X) / layer (Y) / layer (X) / layer (Y) / layer (X), and the like. .

The thickness of the multilayer film of the present invention is not particularly limited, but is preferably 0.2 to 3 mm, more preferably 0.25 to 2.5 mm, and further preferably 0.3 to 2 mm. If the thickness is less than 0.2 mm, the mechanical strength may be insufficient. When thickness exceeds 3 mm, there exists a possibility that a softness | flexibility may become inadequate.

An interlayer film for laminated glass comprising the multilayer film of the present invention is a preferred embodiment of the present invention. When the interlayer film for laminated glass of the present invention is used for an application where it is necessary to appropriately adjust the adhesiveness with glass, an adhesiveness adjusting agent may be contained in the layer (X). As the adhesion adjusting agent, conventionally known ones can be used. For example, acetic acid, propionic acid, butanoic acid, hexanoic acid, 2-ethylbutanoic acid, sodium salt of organic acid such as 2-ethylhexanoic acid, potassium salt, A magnesium salt or the like is used. These can be used alone or in combination of two or more. The optimum content of the adhesion modifier varies depending on the adhesion modifier used, but the adhesion of the resulting film to glass is determined by the Pummel test (described in International Publication No. WO2003 / 033583). In general, it is preferable to adjust to 3 to 10. In particular, when high penetration resistance is required, the content is preferably adjusted to 3 to 6, and when high glass scattering prevention property is required, the content is adjusted to 7 to 10. It is preferable. When high glass scattering prevention property is required, it is also a useful method not to add an adhesion modifier. Usually, the content of the adhesion adjusting agent in the layer (X) is preferably 0.0001 to 1% by mass, more preferably 0.0005 to 0.1% by mass, and 0.001 to 0.03. More preferred is mass%.

Further, as another adjusting agent for adjusting the adhesiveness, a silane coupling agent can be mentioned. The content of the silane coupling agent in the layer (X) is preferably 0.01 to 5% by mass.

The shape of the surface of the interlayer film for laminated glass is not particularly limited. However, in consideration of the handleability (foam removal property) when laminating with glass, the surface in contact with the glass is melted, embossed, or the like by a conventionally known method. It is preferable that an uneven structure is formed. The emboss height is not particularly limited, but is preferably 5 μm to 500 μm, more preferably 7 μm to 300 μm, and still more preferably 10 μm to 200 μm. When the embossing height is less than 5 μm, bubbles formed between the glass and the intermediate film may not be efficiently removed when laminating to glass, and when it exceeds 500 μm, it is difficult to form embossing. Moreover, although embossing may be given to the single side | surface of an intermediate film, and both sides may be sufficient, it is preferable to give normally to both surfaces.

The embossed concavo-convex pattern is not particularly limited as long as it satisfies the specific conditions described above, and may be regularly distributed or randomly distributed.

In order to form such embossing, the embossing roll method, the profile extrusion method,
An extrusion lip embossing method using a melt fracture is employed. In particular, the embossing roll method is suitable for stably obtaining an embossed film on which uniform and fine irregularities are formed.

The embossing roll used in the embossing roll method can be produced by, for example, using an engraving mill (mother mill) having a desired concavo-convex pattern and transferring the concavo-convex pattern onto the surface of the metal roll. It can also be produced using laser etching. Further, after forming a fine concavo-convex pattern on the roll surface as described above, blasting is performed on the surface using an abrasive such as aluminum oxide, silicon oxide, or glass beads to form a finer concavo-convex pattern. You can also.

Also, the embossing roll used in the embossing roll method is preferably subjected to a release treatment. When a roll without mold release treatment is used, troubles that cannot be peeled off from the roll easily occur depending on conditions. For the release treatment, known techniques such as silicone treatment, Teflon (registered trademark) treatment, plasma treatment and the like can be used.

A laminated glass obtained by bonding a plurality of glass plates using the interlayer film for laminated glass is a preferred embodiment of the present invention. The laminated glass can be produced by sandwiching the intermediate film between at least two glass plates and heating and bonding the intermediate film. The glass used for the laminated glass is not particularly limited. In addition to inorganic glass such as float plate glass, tempered plate glass, polished plate glass, mold plate glass, netted plate glass, heat ray absorbing plate glass, conventionally known polymethyl methacrylate, polycarbonate and the like. Organic glass or the like can be used. These may be colorless, colored, transparent or non-transparent. Moreover, these may be used independently and may use 2 or more types together. Although the thickness of glass is not specifically limited, It is preferable that it is 100 mm or less. The shape of the glass is not particularly limited, and may be a simple flat plate glass or a glass having a curvature such as an automobile windshield.

The laminated glass can be produced by a conventionally known method, and examples thereof include a method using a vacuum laminator device, a method using a vacuum bag, a method using a vacuum ring, and a method using a nip roll. Further, there is a method in which the obtained laminate is put into an autoclave after being temporarily pressed using these methods.

In the case of using a vacuum laminator, an example of the production conditions is as follows. The glass and the interlayer film are heated at a temperature of 100 to 200 ° C., particularly 130 to 160 ° C. under a reduced pressure of 1 × 10 ⁻⁶ to 3 × 10 ⁻² MPa. Laminated. A method using a vacuum bag or a vacuum ring is described in, for example, European Patent No. 1235683, and is laminated at 130 to 145 ° C. under a pressure of about 2 × 10 ⁻² MPa, for example.

As a production method using a nip roll, degassing is performed by a roll at a temperature not higher than the flow start temperature of the resin composition containing the polyvinyl acetal (I), ultraviolet absorber and plasticizer used for the production of the layer (X) described above. Then, a method of performing pressure bonding at a temperature close to the flow start temperature can be mentioned. Specifically, for example, there is a method of heating to 30 to 70 ° C. with an infrared heater or the like, then degassing with a roll, further heating to 50 to 120 ° C., and then pressing with a roll.

When pressure bonding is performed using the above-described method, and then further pressure bonding is performed, the operating conditions of the autoclave process are appropriately selected depending on the thickness and configuration of the laminated glass. For example, 1.0 to 1.5 MPa The treatment is preferably carried out at a temperature of 130 to 145 ° C. for 0.5 to 3 hours under pressure.

The multilayer film of the present invention is less colored by heating and less foreign matter (undissolved part). Therefore, the multilayer film of the present invention is excellent in recyclability. Hereinafter, the manufacturing method of the film using the collection | recovery of the said multilayer film is demonstrated.

A method for producing a monolayer film in which a multilayer film recovery product of the present invention (hereinafter, the “multilayer film recovery product of the present invention” may be abbreviated as “collection product”) is melt-kneaded and then formed into a film. Is also a preferred embodiment of the present invention. At this time, the recovered product was a polyvinyl acetal having a degree of acetalization of 55 to 85 mol%, a vinyl ester monomer unit content of 0.1 to 15 mol%, and a viscosity average polymerization degree of 1400 to 5000 ( It is more preferable to form a film after melt-kneading III) and the plasticizer.

Polyvinyl acetal (III) has a viscosity average polymerization degree of 1400 to 5000, preferably 1500 to 3500. When the viscosity average degree of polymerization is less than 1400, the strength of the obtained multilayer film is insufficient. On the other hand, when the polymerization degree exceeds 5000, the melt viscosity becomes too high and film formation becomes difficult.

The degree of acetalization of polyvinyl acetal (III) is 55 to 85 mol%. When the degree of acetalization is less than 55 mol%, the compatibility with a plasticizer or the like decreases. Moreover, there exists a possibility that the foreign material (undissolved part) in the obtained multilayer film may increase. The degree of acetalization is preferably 60 mol% or more, more preferably 65 mol% or more. On the other hand, when the degree of acetalization exceeds 85 mol%, the efficiency of the acetalization reaction is significantly reduced. Moreover, there exists a possibility that the film obtained may become easy to color. The degree of acetalization is preferably 80 mol% or less.

The content of the vinyl ester monomer unit of polyvinyl acetal (III) is 0.1 to 15 mol%. When the content of the vinyl ester monomer unit is less than 0.1 mol%, the polyvinyl acetal cannot be stably produced and the film cannot be formed. The content of the vinyl ester monomer unit is preferably 0.7 mol% or more, more preferably 6 mol% or more, and further preferably 7 mol% or more. On the other hand, when the content of the vinyl ester monomer unit exceeds 15 mol%, the resulting multilayer film is colored. The content of the vinyl ester monomer unit is preferably 13 mol% or less, more preferably 10 mol% or less, and still more preferably 10 mol% or less. When the content of the vinyl ester monomer unit is within these ranges, the layer (Y ′) used in the multilayer film using the recovery film described later becomes a soft layer, and the resulting multilayer film is Excellent sound insulation performance while maintaining practical mechanical strength

The content of the vinyl alcohol monomer unit of the polyvinyl acetal (III) used in the present invention is preferably 5 to 44.9 mol%.

The content of monomer units other than acetalized monomer units, vinyl ester monomer units and vinyl alcohol monomer units in the polyvinyl acetal (III) used in the present invention is preferably 20 mol. % Or less, more preferably 10 mol% or less, and further preferably 5 mol% or less.

The polyvinyl acetal (III) used in the present invention is preferably produced in the same manner as described above as a method for producing the polyvinyl acetal (I) and the polyvinyl acetal (II).

The polyvinyl acetal (I) and the polyvinyl acetal (II) described above are preferably used as the polyvinyl acetal (III). From the viewpoint of further improving the strength of the single layer film, it is preferable to use polyvinyl acetal (I) as polyvinyl acetal (III).

Usually, the film formation of polyvinyl acetal is carried out, for example, in a film formation apparatus in which an extruder is equipped with a measuring machine such as a gear pump and a die such as a T die. Generally, in film formation, both ends (trims) of the film are cut off. It is very important to collect and reuse such trims from the viewpoints of energy saving, effective utilization of resources and improvement of yield. In addition, off-spec products that are difficult to use as products produced when manufacturing films with irregularities on the surface and off-spec products that are difficult to use as products due to non-uniform composition and thickness are also the same as trim It is useful because it can be reused. When the polyvinyl acetal (I) and the polyvinyl acetal (II) used in the multilayer film of the present invention are used, the formation of coarse particles is suppressed during the acetalization reaction, and as a result, the resulting polyvinyl acetal is melt-formed. In addition, a film with reduced foreign matter (undissolved content) can be obtained. Moreover, since the multilayer film of the present invention is less colored when heat-treated, it is possible to effectively reuse the collected materials such as the trim and off-spec products.

As the plasticizer newly added to the recovered material, those described above as used in the production of the layer (X) are used. As the plasticizer to be newly added, any of the aforementioned plasticizers can be used as long as the resulting single layer film has excellent transparency. When the amount of the recovered product exceeds 50 parts by mass with respect to 100 parts by mass of newly added polyvinyl acetal (III), 10 parts by mass or more of the added plasticizer is an aliphatic ester having a hydroxyl group. It is preferable to use a compound, an aliphatic ether compound having a hydroxyl group, an aliphatic polyester compound having a hydroxyl group, a monoether compound of a polyalkylene glycol and an aromatic alcohol, or a monoester compound of a polyalkylene glycol and an aromatic carboxylic acid.

The ratio of the recovered material to the newly added polyvinyl acetal (III) is not particularly limited, and can be arbitrarily changed. Usually, the recovered material is 1 to 10000 parts by mass with respect to 100 parts by mass of polyvinyl acetal (III).

The content of the plasticizer added to the recovered material is not particularly limited, but is preferably 20 to 100 parts by mass with respect to 100 parts by mass of newly added polyvinyl acetal (III). If it is less than 20 mass parts, the impact resistance of the film obtained and the laminated glass manufactured using the said film may become inadequate. On the other hand, if it exceeds 100 parts by mass, the plasticizer may bleed out, and the transparency of the resulting film may be lowered, or the adhesion to glass may be impaired.

As the melt-kneading method and the film forming method employed in the method for producing a single layer film using the recovered material, the method described above as the method used when producing the layer (X) is used. As a method of feeding the recovered material back into the extruder, a method in which a film of a trim or off-spec product is wound on a roll is unwound as it is and then fed back into the extruder; the trim or off-spec product is taken up on a roll. For example, there is a method of cutting the cake into a certain size and then re-feeding it into the extruder.

When reusing collected materials such as trims or off-spec products, adjust the amount of polyvinyl acetal (III), plasticizer, and other components to the extruder while analyzing the newly obtained film components. A desired film can be obtained while adjusting the amount of each added.

The thickness of the monolayer film obtained by the production method using the recovered material is not particularly limited, but is preferably 0.05 to 5.0 mm, more preferably 0.1 to 2.0 mm, More preferably, it is 1 to 1.2 mm.

An interlayer film for laminated glass composed of a single layer film obtained by a production method using the recovered material is also a preferred embodiment of the present invention. The single layer film is less colored. Moreover, since the said single layer film has few foreign materials (undissolved part), the said single layer film is excellent in transparency. Therefore, the single layer film is useful as an interlayer film for laminated glass. A laminated glass obtained by bonding a plurality of glass plates using the interlayer film for laminated glass is also a preferred embodiment of the present invention. The said laminated glass can be manufactured by the method mentioned above as a manufacturing method of the laminated glass which used the multilayer film of this invention as an intermediate film.

It is preferable that the haze of the laminated glass thus obtained is 1.0 or less. In the present invention, the haze of the laminated glass is measured according to JIS K7105.

Of the layer (Y ′) formed by melting and kneading the recovered material, polyvinyl acetal (III), plasticizer, heat ray shielding fine particles, surfactant, and alkali metal salt and / or alkaline earth metal salt. A preferred embodiment of the present invention is a method for producing a multilayer film in which a layer (X) formed by melting and kneading a polyvinyl acetal (I), an ultraviolet absorber, and a plasticizer is disposed on both outer sides. is there.

Here, as the polyvinyl acetal (III), those described above as being used for a monolayer film obtained using the recovered material are used. As polyvinyl acetal (III), it is preferable to use the above-mentioned polyvinyl acetal (I) and polyvinyl acetal (II). From the viewpoint of further improving sound insulation, it is preferable to use polyvinyl acetal (II) as polyvinyl acetal (III).

As the plasticizer, heat ray shielding fine particles, surfactant, alkali metal salt and alkaline earth metal salt added to the recovered material, those described above as those used for the production of the layer (Y) are used.

Any of the plasticizers described above as used for the production of the layer (Y) can be used as long as the obtained single layer film has excellent transparency. When the amount of the recovered product exceeds 50 parts by mass with respect to 100 parts by mass of newly added polyvinyl acetal (III), 10 parts by mass or more of the added plasticizer is an aliphatic ester having a hydroxyl group. It is preferable to use a compound, an aliphatic ether compound having a hydroxyl group, an aliphatic polyester compound having a hydroxyl group, a monoether compound of a polyalkylene glycol and an aromatic alcohol, or a monoester compound of a polyalkylene glycol and an aromatic carboxylic acid.

The amount of the plasticizer to be newly added is preferably 20 to 100 parts by mass with respect to 100 parts by mass of the newly added polyvinyl acetal (III). If it is less than 20 mass parts, the impact resistance of a multilayer film and the laminated glass obtained may become inadequate. On the other hand, when the amount exceeds 100 parts by mass, the plasticizer may bleed out and the transparency of the resulting multilayer film may be reduced, or the adhesion to glass may be impaired.

The amount of the heat ray shielding fine particles added is preferably 0.001 to 2 parts by mass with respect to 100 parts by mass of the total amount of plasticizer and polyvinyl acetal (III) to be newly added. If the content is 0.001 part by mass or less, the expected heat ray shielding effect may not be obtained. More preferably, it is 0.002 mass part or more, More preferably, it is 0.005 mass part or more. Moreover, when content exceeds 2 mass parts, there exists a possibility that transparency of the multilayer film obtained may be impaired. More preferably, it is 1.5 mass parts or less, More preferably, it is 1 mass part or less.

The addition amount of the surfactant is preferably 0.005 to 2 parts by mass with respect to 100 parts by mass of the total amount of polyvinyl acetal (III) and plasticizer to be newly added. When the content is less than 0.005 parts by mass, the effect of dispersing the heat ray shielding fine particles may not be sufficiently obtained. More preferably, it is 0.05 mass part or more, More preferably, it is 0.1 mass part or more. Moreover, when it exceeds 2 mass parts, the bleed-out of surfactant will be remarkable and the adhesive force with respect to glass may not be hold | maintained stably. More preferably, it is 1.8 parts by mass or less.

The amount of the alkali metal salt and / or alkaline earth metal salt added to the recovered material is the content of the alkali metal and / or alkaline earth metal derived from the alkali metal salt and / or alkaline earth metal salt. Is preferably 0.006 to 0.2 parts by mass with respect to 100 parts by mass of polyvinyl acetal (III). If it is less than 0.006 parts by mass, deterioration of the resin derived from the surfactant may not be sufficiently suppressed. More preferably, it is 0.008 mass part or more. Moreover, when content exceeds 0.2 mass part, aggregation of a heat ray shielding fine particle will be accelerated | stimulated and the transparency of the multilayer film obtained as a result may be lost. More preferably, it is 0.1 mass part or less, More preferably, it is 0.04 mass part or less.

The layer (Y ′) can be produced by the method described above as the production method of the layer (Y) except that polyvinyl acetal (III) and the recovered material are used instead of polyvinyl acetal (II). Here, as a method of feeding the recovered material into the extruder again, a method in which a film of a trim or off-spec product is wound on a roll is unwound as it is and then fed back into the extruder; the trim or off-spec product is rolled. For example, a method of cutting the wound material into a certain size and then re-feeding it into the extruder may be mentioned. The multilayer film using the recovered material is the method described above as the method for producing a laminated film having the layer (X) and the layer (Y) except that the layer (Y ′) is used instead of the layer (Y). It can be manufactured in the same manner.

The multilayer structure and thickness of the multilayer film using the recovered material are the multilayer film having the layer (X) and the layer (Y) described above, except that the layer (Y ′) is used instead of the layer (Y). The same.

An interlayer film for laminated glass made of a multilayer film obtained by the method for producing a multilayer film using the recovered material is a preferred embodiment of the present invention. Since the multilayer film using the recovered material has few foreign matters (undissolved content), the multilayer film is excellent in transparency. Therefore, the multilayer film is useful as an interlayer film for laminated glass. A laminated glass obtained by bonding a plurality of glass plates using the interlayer film for laminated glass is also a preferred embodiment of the present invention. The said laminated glass can be manufactured by the method mentioned above as a manufacturing method of the laminated glass which used the multilayer film which has layer (X) and layer (Y) as an intermediate film. The haze of the laminated glass thus obtained is preferably 1.0 or less.

Hereinafter, the present invention will be described in more detail with reference to examples and comparative examples. In the following examples and comparative examples, “parts” and “%” are based on mass unless otherwise specified. “Polymerization degree” means “viscosity average polymerization degree”.

[Synthesis of polyvinyl acetate]
PVAc-1
A 6 L separable flask equipped with a stirrer, thermometer, nitrogen introduction tube, and reflux tube was deoxygenated in advance, and vinyl acetate monomer (VAM) 2555 g containing 500 ppm acetaldehyde (AA) and 50 ppm acetaldehyde dimethyl acetal (DMA). 945 g of methanol (MeOH) containing 50 ppm of acetaldehyde dimethyl acetal and an acetaldehyde content of less than 1 ppm; 1% methanol solution of tartaric acid in an amount of 20 ppm of tartaric acid in the vinyl acetate monomer was charged. While blowing nitrogen into the flask, the temperature inside the flask was adjusted to 60 ° C. Note that an ethylene glycol / water solution at −10 ° C. was circulated in the reflux tube. A 0.55% by mass methanol solution of di-n-propyl peroxydicarbonate was prepared, and 18.6 mL was added to the flask to initiate polymerization. At this time, the amount of di-n-propyl peroxydicarbonate added was 0.081 g. A methanol solution of di-n-propyl peroxydicarbonate was sequentially added at a rate of 20.9 mL / hour until the completion of polymerization. During the polymerization, the temperature in the flask was kept at 60 ° C. Four hours after the start of the polymerization, when the solid content concentration of the polymerization solution reached 25.1%, 0.0141 g of sorbic acid (3% of di-n-propyl peroxydicarbonate remaining undecomposed in the polymerization solution) was obtained. After adding 1200 g of contained methanol (corresponding to a molar equivalent), the polymerization solution was cooled to stop the polymerization. When the polymerization was stopped, the polymerization rate of the vinyl acetate monomer was 35.0%. After the polymerization solution was cooled to room temperature, the inside of the flask was depressurized using a water aspirator to distill off the vinyl acetate monomer and methanol, thereby precipitating polyvinyl acetate. 3000 g of methanol was added to the precipitated polyvinyl acetate, and the polyvinyl acetate was dissolved while heating at 30 ° C., and then the inside of the flask was decompressed again using a water aspirator to distill off the vinyl acetate monomer and methanol. Thus, polyvinyl acetate was precipitated. The operation of dissolving polyvinyl acetate in methanol and then precipitating it was further repeated twice. Methanol was added to the precipitated polyvinyl acetate to obtain a 40% by mass methanol solution of polyvinyl acetate (PVAc-1) with a vinyl acetate monomer removal rate of 99.8%.

The polymerization degree was measured using a part of the methanol solution of PVAc-1 obtained. A 10% methanol solution of sodium hydroxide was added to the methanol solution of PVAc-1 so that the molar ratio of sodium hydroxide to vinyl acetate units in polyvinyl acetate was 0.1. When the gelled product was formed, the gel was pulverized and subjected to Soxhlet extraction with methanol for 3 days. The obtained polyvinyl alcohol was dried and subjected to viscosity average polymerization degree measurement. The degree of polymerization was 1700.

PVAc-2 to PVAc-12
Polyvinyl acetate (PVAc-2 to PVAc-12) was obtained in the same manner as PVAc-1, except that the conditions were changed to those described in Table 1. In Table 1, “ND” means less than 1 ppm. The degree of polymerization of each polyvinyl acetate obtained was determined in the same manner as PVAc-1. The results are shown in Table 1.

[Synthesis of polyvinyl alcohol]
PVA-1
Water with respect to vinyl acetate monomer units in methanol and polyvinyl acetate so that the total solid concentration (saponification concentration) is 30% by mass with respect to a 40% by mass methanol solution of polyvinyl acetate in PVAc-1. An 8% methanol solution of sodium hydroxide was added with stirring so that the molar ratio of sodium oxide was 0.020, and the saponification reaction was started at 40 ° C. The gel is pulverized when the gelated product is generated as the saponification reaction proceeds, and the crushed gel is transferred to a container at 40 ° C. When 60 minutes have elapsed from the start of the saponification reaction, methanol / methyl acetate / water ( 25/70/5 mass ratio) solution and neutralized. The obtained swollen gel was centrifuged, and methanol twice as much as the swollen gel was added, immersed, left for 30 minutes, and then centrifuged four times, 60 ° C. for 1 hour, 100 PVA-1 was obtained by drying at 2 ° C. for 2 hours.

The polymerization degree and saponification degree of PVA-1 were determined by the method described in JIS-K6726. The degree of polymerization was 1700, and the degree of saponification was 99.1 mol%. These physical property data are also shown in Table 2.

After ashing PVA-1, the sodium acetate content of PVA-1 was determined by measuring the amount of sodium in the obtained ash using an ICP emission analyzer “IRIS AP” manufactured by Jarrel Ash. . The sodium acetate content was 0.7% (0.20% in terms of sodium). These physical property data are also shown in Table 2.

PVA-2 ~ 5, comparative PVA-1 ~ 3
Each PVA was synthesized in the same manner as PVA-1, except that the conditions shown in Table 2 were changed. The polymerization degree, saponification degree, and sodium acetate content (sodium mass conversion) of the obtained PVA were measured in the same manner as PVA-1. The results are shown in Table 2.

PVA-6, comparative PVA-4 and 5
Each PVA was synthesized in the same manner as PVA-1, except that the conditions shown in Table 3 were changed. The polymerization degree, saponification degree, and sodium acetate content (sodium mass conversion) of the obtained PVA were measured in the same manner as PVA-1. The results are shown in Table 3.

PVA-7, comparative PVA-6 and 7
Each PVA was synthesized in the same manner as PVA-1, except that the conditions shown in Table 4 were changed. The polymerization degree, saponification degree, and sodium acetate content (sodium mass conversion) of the obtained PVA were measured in the same manner as PVA-1. The results are shown in Table 4.

PVA-8-11, comparative PVA-8 and 9
Each PVA was synthesized in the same manner as PVA-1, except that the conditions shown in Table 5 were changed. The polymerization degree, saponification degree, and sodium acetate content (sodium mass conversion) of the obtained PVA were measured in the same manner as PVA-1. The results are shown in Table 5.

PVA-12, comparative PVA-10 and 11
Each PVA was synthesized in the same manner as PVA-1 except that the conditions were changed to those shown in Table 6. The polymerization degree, saponification degree, and sodium acetate content (sodium mass conversion) of the obtained PVA were measured in the same manner as PVA-1. The results are shown in Table 6.

PVA-13, comparative PVA-12 and 13
Each PVA was synthesized in the same manner as PVA-1, except that the conditions shown in Table 7 were changed. The polymerization degree, saponification degree, and sodium acetate content (sodium mass conversion) of the obtained PVA were measured in the same manner as PVA-1. The results are shown in Table 7.

[Synthesis of PVB]
PVB-1
A 10-liter glass container equipped with a reflux condenser, thermometer, and squid-type stirring blade was charged with 8100 g of ion-exchanged water and 660 g of PVA-1 (PVA concentration 7.5%), and the content was raised to 95 ° C. Warm to completely dissolve the PVA. Next, the contents were gradually cooled to 10 ° C. over about 30 minutes while stirring at 120 rpm, and then 384 g of n-butyraldehyde and 540 mL of 20% hydrochloric acid were added to the vessel, and a butyralization reaction was performed for 150 minutes. It was. Thereafter, the temperature was raised to 60 ° C. over 60 minutes, held at 60 ° C. for 120 minutes, and then cooled to room temperature. The precipitated resin was washed with ion-exchanged water and then neutralized by adding an excessive amount of aqueous sodium hydroxide solution. Subsequently, the resin was washed again with ion-exchanged water and dried to obtain PVB-1.

[Composition of PVB]
The degree of butyralization (degree of acetalization) of PVB-1, the content of vinyl acetate monomer units, and the content of vinyl alcohol monomer units were measured according to JIS K6728. The degree of butyralization (degree of acetalization) was 68.2 mol%, the content of vinyl acetate monomer units was 0.9 mol%, and the content of vinyl alcohol monomer units was 30.9 mol%. It was. The results are also shown in Table 8.

PVB-2 ~ 5
PVB was synthesized and evaluated in the same manner as PVB-1, except that the raw material PVA was changed to that shown in Table 8. The results are shown in Table 8.

PVB-6
PVB was synthesized and evaluated in the same manner as PVB-1, except that the amount of n-butyraldehyde added was changed to 320 g. The results are shown in Table 8.

PVB-7
PVB was synthesized and evaluated in the same manner as PVB-1, except that the amount of n-butyraldehyde added was changed to 362 g. The results are shown in Table 8.

PVB-8
Polyvinyl butyral was synthesized and evaluated in the same manner as PVB-1, except that the amount of n-butyraldehyde added was changed to 449 g. The results are shown in Table 8.

Comparison PVB-1 ~ 3
Polyvinyl butyral was synthesized and evaluated in the same manner as PVB-1, except that the raw material PVA was changed to that shown in Table 8. The results are shown in Table 8.

Comparison PVB-4
Polyvinyl butyral was synthesized and evaluated in the same manner as PVB-6 except that the raw material PVA was changed to comparative PVA-1. The results are shown in Table 8.

Comparative PVB-5
Polyvinyl butyral was synthesized and evaluated in the same manner as PVB-8, except that the raw material PVA was changed to comparative PVA-1. The results are shown in Table 8.

Comparative PVB-6
Polyvinyl butyral was synthesized and evaluated in the same manner as PVB-6 except that the raw material PVA was changed to comparative PVA-2. The results are shown in Table 8.

Comparative PVB-7
Polyvinyl butyral was synthesized and evaluated in the same manner as PVB-8, except that the raw material PVA was changed to comparative PVA-2. The results are shown in Table 8.

PVB-9
A 10-liter glass container equipped with a reflux condenser, thermometer and squid type stirring blade was charged with 8234 g of ion-exchanged water and 526 g of PVA-6 (PVA concentration 6.0%), and the contents were raised to 95 ° C. Warm to dissolve completely. Next, the contents were gradually cooled to 15 ° C. over about 30 minutes while stirring at 120 rpm, and then 307 g of n-butyraldehyde and 540 mL of 20% hydrochloric acid were added to the vessel, and a butyralization reaction was performed for 120 minutes. It was. Thereafter, the temperature was raised to 60 ° C. over 60 minutes, held at 60 ° C. for 120 minutes, and then cooled to room temperature. The precipitated resin was washed with ion-exchanged water and then neutralized by adding an excessive amount of aqueous sodium hydroxide solution. Subsequently, it was rewashed with ion-exchanged water and dried to obtain polyvinyl butyral.

The composition of the obtained polyvinyl butyral was measured in the same manner as PVB-1. The degree of butyralization (degree of acetalization) was 68.2 mol%, the content of vinyl acetate monomer units was 1.3 mol%, and the content of vinyl alcohol monomer units was 30.5 mol%. It was. Next, GPC measurement of the obtained PVB-9 was performed in the same manner as PVB-1. Table 9 shows the evaluation results.

Comparative PVB-8 and 9
PVB was synthesized and evaluated in the same manner as PVB-9, except that the raw material PVA was changed to that shown in Table 9. The results are shown in Table 9.

PVB-10
A 10-liter glass container equipped with a reflux condenser, thermometer and squid type stirring blade was charged with 8322 g of ion-exchanged water and 438 g of PVA-7 (PVA concentration 5.0%), and the contents were raised to 95 ° C. Warm to completely dissolve the PVA. Next, the contents are gradually cooled to 20 ° C. over about 30 minutes while stirring at 120 rpm, and then 256 g of n-butyraldehyde and 540 mL of 20% hydrochloric acid are added to the vessel, and a butyralization reaction is performed for 120 minutes. It was. Thereafter, the temperature was raised to 60 ° C. over 60 minutes, held at 60 ° C. for 120 minutes, and then cooled to room temperature. The precipitated resin was washed with ion-exchanged water and then neutralized by adding an excessive amount of aqueous sodium hydroxide solution. Subsequently, PVB was obtained by re-washing with ion-exchanged water and drying.

The composition of the obtained PVB was measured in the same manner as PVB-1. The degree of butyralization (degree of acetalization) was 68.1 mol%, the content of vinyl acetate monomer units was 1.5 mol%, and the content of vinyl alcohol monomer units was 30.4 mol%. It was. Next, GPC measurement of the obtained PVB-10 was performed in the same manner as PVB-1. Table 10 shows the evaluation results.

Comparative PVB-10 and 11
PVB was synthesized and evaluated in the same manner as PVB-10 except that the raw material PVA was changed to that shown in Table 10. The results are shown in Table 10.

PVB-11
A 10-liter glass container equipped with a reflux condenser, thermometer, and squid type stirring blade was charged with 8100 g of ion-exchanged water and 660 g of PVA-8 (PVA concentration 7.5%), and the contents were raised to 95 ° C. Warm to dissolve completely. Next, the contents are gradually cooled to 15 ° C. over about 30 minutes while stirring at 120 rpm, and then 432 g of n-butyraldehyde and 540 mL of 20% hydrochloric acid are added to the vessel, and a butyralization reaction is performed for 90 minutes. It was. Thereafter, the temperature was raised to 45 ° C. over 30 minutes, held at 45 ° C. for 180 minutes, and then cooled to room temperature. The precipitated resin was washed with ion-exchanged water and then neutralized by adding an excessive amount of aqueous sodium hydroxide solution. Subsequently, PVB was obtained by re-washing with ion-exchanged water and drying.

The composition of the obtained PVB was measured in the same manner as PVB-1. The degree of butyralization (degree of acetalization) was 74.1 mol%, the content of vinyl acetate monomer units was 8.1 mol%, and the content of vinyl alcohol monomer units was 17.8 mol%. It was. GPC measurement of the obtained PVB-11 was performed in the same manner as PVB-1. The evaluation results are shown in Table 11.

PVB-12-14
PVB was synthesized and evaluated in the same manner as PVB-11 except that the raw material PVA was changed to that shown in Table 11. The results are shown in Table 11.

PVB-15
PVB was synthesized and evaluated in the same manner as PVB-11 except that the amount of n-butyraldehyde added was changed to 458 g. The results are shown in Table 11.

Comparative PVB-12 and 13
PVB was synthesized and evaluated in the same manner as PVB-11 except that the raw material PVA was changed to that shown in Table 11. The results are shown in Table 11.

Comparative PVB-14 and 15
PVB was synthesized and evaluated in the same manner as PVB-15 except that the raw material PVA was changed to that shown in Table 11. The results are shown in Table 11.

PVB-16
A 10 L liter glass container equipped with a reflux condenser, thermometer, and squid type stirring blade was charged with 8234 g of ion-exchanged water and 526 g of PVA-12 (PVA concentration 6.0%), and the contents were raised to 95 ° C. Warm to completely dissolve the PVA. Next, the contents are gradually cooled to 15 ° C. over about 60 minutes while stirring at 120 rpm, and then 344 g of n-butyraldehyde and 540 mL of 20% hydrochloric acid are added to the vessel, and a butyralization reaction is performed for 90 minutes. It was. Thereafter, the temperature was raised to 45 ° C. over 30 minutes, held at 45 ° C. for 180 minutes, and then cooled to room temperature. The precipitated resin was washed with ion-exchanged water and then neutralized by adding an excessive amount of aqueous sodium hydroxide solution. Subsequently, PVB was obtained by re-washing with ion-exchanged water and drying.

The composition of the obtained PVB was measured in the same manner as PVB-1. The degree of butyralization (degree of acetalization) was 74.6 mol%, the content of vinyl acetate monomer units was 8.3 mol%, and the content of vinyl alcohol monomer units was 17.1 mol%. It was. GPC measurement of the obtained PVB-16 was performed in the same manner as PVB-1. The evaluation results are shown in Table 12.

Comparative PVB-16 and 17
PVB was synthesized and evaluated in the same manner as PVB-16 except that the raw material PVA was changed to that shown in Table 12. The results are shown in Table 12.

PVB-17
A 10-liter glass container equipped with a reflux condenser, thermometer, and squid-type stirring blade was charged with 8234 g of ion-exchanged water and 438 g of PVA-13 (PVA concentration 5.0%), and the contents were raised to 95 ° C. Warm to completely dissolve the PVA. Next, the contents are gradually cooled to 15 ° C. over about 60 minutes while stirring at 120 rpm, and then 265 g of n-butyraldehyde and 540 mL of 20% hydrochloric acid are added to the vessel, and a butyralization reaction is performed for 90 minutes. It was. Thereafter, the temperature was raised to 45 ° C. over 30 minutes, held at 45 ° C. for 180 minutes, and then cooled to room temperature. The precipitated resin was washed with ion-exchanged water and then neutralized by adding an excessive amount of aqueous sodium hydroxide solution. Subsequently, PVB was obtained by re-washing with ion-exchanged water and drying.

The composition of the obtained PVB was measured in the same manner as PVB-1. The degree of butyralization (average degree of acetalization) of PVB is 73.2 mol%, the content of vinyl acetate monomer units is 8.1 mol%, and the content of vinyl alcohol monomer units is 18.7 mol%. %Met. GPC measurement of the obtained PVB-17 was performed in the same manner as PVB-1. The evaluation results are shown in Table 13.

Comparative PVB-18 and 19
PVB was synthesized and evaluated in the same manner as PVB-17 except that the raw material PVA was changed to that shown in Table 13. The results are shown in Table 13.

Example 1
[Production of Layer (X)]
50 parts by mass of the synthesized PVB-1 powder, 19 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer, and 0.175 parts by mass of “Tinuvin 328” manufactured by Ciba Japan as an ultraviolet absorber, Using a Labo plast mill “C model” manufactured by Toyo Seiki Seisakusho Co., Ltd., melt kneading was performed at 170 ° C. and 50 rpm for 5 minutes. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 320 μm.

[Preparation of layer (Y)]
A ZnSb ₂ O ₆ anhydrous zinc antimonate methanol dispersion (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill to prepare a zinc antimonate methanol dispersion having a concentration of 60% by mass. . 1.62 parts by mass of the obtained dispersion, 0.24 parts by mass of “DISPERBYK-102” manufactured by Big Chemie as phosphate ester, and 12.1 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer The dispersion obtained in this way, 12.2 parts by mass of triethylene glycol-di-2-ethylhexanoate, a 25% by mass aqueous solution 0.10 of a mixture of magnesium acetate and potassium acetate (mixing mass ratio: 2/1) 0.10 Mass parts and 43 parts by mass of the synthesized PVB-11 powder were melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using the Laboplast mill. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 120 μm.

[Production of multilayer film]
Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 μm under conditions of 135 ° C. and 10 kg / cm ^2. A multilayer film composed of (X) (320 μm) / layer (Y) (120 μm) / layer (X) (320 μm) was obtained.

[GPC measurement]
(measuring device)
GPC measurement was performed using “GPCmax” manufactured by VISCOTECH. As a differential refractive index detector, “TDA305” manufactured by VISCOTECH was used. “UV Detector 2600” manufactured by VISCOTECH was used as an ultraviolet-visible absorption detector. The optical path length of the detection cell of the absorptiometric detector is 10 mm. As the GPC column, “GPC HFIP-806M” manufactured by Showa Denko KK was used. Moreover, OmniSEC (Version 4.7.0.406) attached to the apparatus was used as analysis software.

(Measurement condition)
As the mobile phase, HFIP containing 20 mmol / l sodium trifluoroacetate was used. The mobile phase flow rate was 1.0 ml / min. The sample injection amount was 100 μl, and measurement was performed at a GPC column temperature of 40 ° C.

In addition, the sample in which the PVA viscosity average polymerization degree in a sample exceeded 2400 performed GPC measurement using the sample (100 microliters) diluted suitably. The absorbance at a sample concentration of 1.00 mg / ml was calculated from the measured value according to the following formula. α (mg / ml) is the concentration of the diluted sample.

Absorbance at a sample concentration of 1.00 mg / ml = (1.00 / α) × measured value of absorbance

(Create a calibration curve)
As a standard, monodispersed PMMA (peak top molecular weight: 1944000, 790000, 467400, 271400, 144000, 79250, 35300, 13300, 7100, 1960, 1020, 690) manufactured by Agilent Technologies was measured, and a differential refractive index detector. A calibration curve for converting the elution volume into the PMMA molecular weight was prepared for each of the absorptiometric detectors. The analytical software was used to create each calibration curve. In this measurement, a column in a state where the peaks of standard samples having both molecular weights of 1944000 and 271400 can be separated in the PMMA measurement is used.

In this apparatus, the signal intensity obtained from the differential refractive index detector is expressed in millivolts, and the signal intensity obtained from the absorptiometric detector is expressed in absorbance (abs unit: Absorbance unit).

(Sample adjustment)
The resulting multilayer film was heated by hot pressing at 2 MPa and 230 ° C. for 3 hours, and then cooled to obtain a heat-treated film. A film piece obtained by cutting perpendicularly to the surface of the film from the center was used as a sample.

(Measurement)
The obtained sample was dissolved in HFIP containing 20 mmol / l sodium trifluoroacetate to prepare a solution (concentration 1.00 mg / ml) in which the sample was dissolved. The solution was filtered through a 0.45 μm polytetrafluoroethylene filter and then subjected to GPC measurement. At this time, a chromatogram in which the signal intensity measured by the differential refractive index detector is plotted with respect to the molecular weight converted from the elution volume (PMMA converted molecular weight) is prepared, and the peak top molecular weight (A) and the peak top molecular weight are prepared. The signal intensity (a) in (A) was determined. Also, a chromatogram in which the signal intensity (absorbance) measured with an absorptiometer (measurement wavelength 280 nm) is plotted against the molecular weight (PMMA equivalent molecular weight) is created, and the peak top molecular weight (B) and peak top molecular weight The signal intensity (absorbance, b) in (B) was determined.

The obtained peak top molecular weight (A) and peak top molecular weight (B) are expressed by the following formula (AB) / A
The value obtained by substituting for was 0.49. The results are also shown in Table 14.

The signal intensity at the peak top molecular weight (C) and the peak top molecular weight (C) was the same as the method for determining the peak top molecular weight (B) and the signal intensity (absorbance, b) except that the measurement wavelength was changed to 320 nm. (Absorbance, c) was determined. The peak top molecular weight (A) and the peak top molecular weight (C) are expressed by the following formula (AC) / A
The value obtained by substituting for was 0.51. The results are also shown in Table 14.

As a monodispersed PMMA, American Polymer Standard Corp. “PMMA85K” (weight average molecular weight 85450, number average molecular weight 74300, intrinsic viscosity 0.309) manufactured by the company was used. PMMA GPC measurement was performed in the same manner as the above method except that the sample was changed to the PMMA. The signal intensity (x) at the peak top molecular weight measured with a differential refractive index detector, which was determined in the same manner as the method for determining the peak top molecular weight (A), was 390.82 mV. In addition, the signal intensity (absorbance, y) at the peak top molecular weight measured with an absorptiometric detector (220 nm) obtained in the same manner as the method for determining the peak top molecular weight (B) was 269.28 mV (0.26928 absorber). Unit).

Signal intensity (a), peak top molecular weight (b), signal intensity (x) and signal intensity (y) are expressed by the following formula (b / y) / (a / x)
The value obtained by substituting for was 2.82 × 10 ⁻² . The results are also shown in Table 14.

Signal intensity (a), peak top molecular weight (c), signal intensity (x), and signal intensity (y) are represented by the following formula (c / y) / (a / x)
The value obtained by substituting for was 1.60 × 10 ⁻² . The results are also shown in Table 14.

[Undissolved content in the film]
The obtained laminated film was sandwiched between two transparent glass plates (20 cm × 20 cm), and preliminary adhesion was performed by passing a press roll at 110 ° C. while extruding air between the glass plate and the film. The laminated body after the preliminary adhesion was allowed to stand at 135 ° C. and 1.2 MPa for 30 minutes in an autoclave to produce a laminated glass (20 sheets in total). The number of foreign matters in the laminated glass obtained using a magnifying glass was counted by visual observation. The total number of foreign substances in 20 laminated glasses was determined and evaluated according to the following criteria. The results are shown in Table 14.
A: 0 (pieces / 20 sheets)
B: 1 (20 pieces)
C: 2-3 (pieces / 20 pieces)
D: 4-8 (pieces / 20 pieces)
E: 9 or more (pieces / 20 sheets)

[Measurement of visible light transmittance and sunlight transmittance]
A laminated glass was produced in the same manner as in the above “undissolved part in the film”. Using a spectrophotometer “SolidSpec-3700” manufactured by Shimadzu Corporation, the transmittance of the produced laminated glass in the wavelength region of 280 to 2500 nm was measured. Then, according to JIS R3106, a visible light transmittance (%) of 380 to 780 nm was determined. Further, the solar transmittance (%) of 300 to 2500 nm was determined using the weight coefficient described in JIS R3106. The results are shown in Table 14.

[Colorability of film]
The laminated film obtained in “Preparation of laminated film” was heat-treated at 230 ° C., pressure 2 MPa, and 3 hours. The yellowness of the laminated film before the heat treatment and the laminated film after the heat treatment were measured, and the colorability was evaluated from the difference in yellowness (ΔYI) between the two according to the following criteria. The measurement was performed according to JIS K 7105 using an SM color computer “SM-TH” manufactured by Suga Test Instruments Co., Ltd. The results are shown in Table 14.
A: Less than 0.5 B: 0.5 or more and less than 1.0 C: 1.0 or more and less than 2.0 D: 2.0 or more and less than 3.0 E: 3.0 or more

[Production of monolayer film using recovered material]
The laminated film obtained in the above “production of laminated film” was cut into a size of 1 cm × 1 cm. With respect to 100 parts by mass of the cut laminated film, 70 parts by mass of unused PVB-1 powder, and castor oil (glycerin tricarboxylic acid ester, 86% by mass of the carboxylic acid ester part was ricinoleic acid as a plasticizer. 13 mass% is any one of palmitic acid ester, stearic acid ester, oleic acid ester, linoleic acid ester, and linolenic acid ester, and 1 mass% is composed of other carboxylic acid esters; hydroxyl groups per molecule 2.6 number, hydroxyl value 160 mgKOH / g, number average molecular weight based on hydroxyl value 910) at a ratio of 30 parts by mass using a lab plast mill “C model” manufactured by Toyo Seiki Co., Ltd., 180 ° C., 50 rpm For 5 minutes. There was no fuming from the raw material mixture during melt kneading. The kneaded sample was hot-pressed (170 ° C., 30 minutes) to obtain a single-layer film having a size of 20 cm × 20 cm and a thickness of 760 μm.

[Colorability of single-layer film using recovered material]
The single layer film obtained in the above-mentioned “Preparation of Single Layer Film Using Collected Material” was heat-treated at 230 ° C., pressure 2 MPa, and 3 hours. The yellowness of the single-layer film before the heat treatment and the single film after the heat treatment were measured, and the colorability was evaluated from the difference in yellowness (ΔYI) between the two according to the following criteria. The measurement was performed according to JIS K 7105 using an SM color computer “SM-TH” manufactured by Suga Test Instruments Co., Ltd. The results are shown in Table 15.
A: Less than 0.5 B: 0.5 or more and less than 1.0 C: 1.0 or more and less than 2.0 D: 2.0 or more and less than 3.0 E: 3.0 or more

[Haze of single layer film using recovered material]
A single laminated glass was produced from the monolayer film obtained in the above (production of recovered and reused monolayer PVB film) in the same manner as above (undissolved portion in the film). The obtained laminated glass was measured by using the haze meter (HZ-1) manufactured by Suga Test Instruments Co., Ltd., and the haze of the laminated glass-1 was measured and evaluated according to the following evaluation criteria. The results are shown in Table 15.
A: Less than 0.5 B: 0.5 or more and less than 1.0 C: 1.0 or more and less than 2.0 D: 2.0 or more and less than 3.0 E: 3.0 or more

[Preparation of multilayer film using recovered material]
The laminated film obtained in the above “production of laminated film” was cut into a size of 1 cm × 1 cm. With respect to 100 parts by mass of the cut laminated film, 70 parts by mass of PVB-1 powder and castor oil (glycerin tricarboxylic acid ester, 86% by mass of the carboxylic acid ester part being ricinoleic acid ester) as a plasticizer 13% by mass is any one of palmitic acid ester, stearic acid ester, oleic acid ester, linoleic acid ester, and linolenic acid ester, and 1% by mass is composed of other carboxylic acid ester; the number of hydroxyl groups per molecule is 2 .6, hydroxyl value 160 mgKOH / g, number average molecular weight based on hydroxyl value 910) 15 parts by mass, 1.1 parts by mass of the above-mentioned zinc antimonate methanol dispersion having a concentration of 60% by mass, the above-mentioned phosphate ester 0.17 A dispersion obtained by mixing 15 parts by weight of the above-mentioned castor oil and 10 parts by weight of the above-mentioned castor oil Using Seisakusho Laboplastomill "C Model", 180 ° C., for 5 minutes melt-kneaded at 50 rpm. There was no fuming from the raw material mixture during melt kneading. The kneaded sample was hot-pressed (170 ° C., 30 minutes) to obtain a single-layer PVB film having a size of 20 cm × 20 cm and a thickness of 120 μm. This was designated as a layer (Y ′). Layer (X) (320 μm) / Layer (Y ′) (120 μm) / Similar to “Preparation of laminated film” except that the obtained layer (Y ′) was used instead of the layer (Y). A laminated film consisting of the layer (X) (320 μm) was obtained.

[Haze of multilayer film using recovered material]
The haze of the multilayer film using the obtained recovered material was measured in the same manner as in “Haze of single-layer PVB film using recovered material”. The results are shown in Table 15.

[Measurement of visible light transmittance and sunshine transmittance of multilayer film using collected material]
The visible light transmittance and sunshine transmittance of the multilayer film using the collected material were measured in the same manner as in “Haze of single-layer PVB film using collected material”. The results are shown in Table 15.

[Colorability of multilayer film using recovered material]
By the same method as “haze of single layer PVB film using recovered material”, the colorability of the multilayer film using the recovered material was evaluated. The results are shown in Table 15.

Examples 2-5
Each film in the same manner as in Example 1 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 14 and 15, respectively. Were prepared and evaluated. The results are shown in Tables 14 and 15.

Examples 6 and 7
The PVB used for the production of the layer (X) and the PVB added to the recovered material were changed to those shown in Tables 14 and 15, respectively, and the plasticizer used for the production of the layer (X) and the layer (Y) was changed to dibutoxyethyl adipate. Except for the change, each film was produced and evaluated in the same manner as in Example 1. The results are shown in Tables 14 and 15.

Example 8
Each of the PVBs used for the production of the layer (X), the PVBs used for the production of the layer (Y), and the PVBs added to the recovered materials were changed to those shown in Tables 14 and 15, respectively. Film preparation and evaluation were performed. The results are shown in Tables 14 and 15.

Examples 9-11
Each film was produced and evaluated in the same manner as in Example 1 except that the plasticizer added to the recovered material was changed to those shown in Tables 14 and 15, respectively. The results are shown in Tables 14 and 15.

Example 12
Each film was prepared and evaluated in the same manner as in Example 1 except that a tin-doped indium oxide isopropanol dispersion ("ITO isopropanol dispersion" manufactured by Mitsubishi Materials Corporation) was used instead of the zinc antimonate methanol dispersion. . The results are shown in Tables 14 and 15.

Comparative Examples 1 to 3, 5, 7 to 9
Each film in the same manner as in Example 1 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 14 and 15, respectively. Were prepared and evaluated. The results are shown in Tables 14 and 15.

Comparative Examples 4 and 6
The PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB to be added to the recovered material are changed to those shown in Tables 14 and 15, respectively. Each film was produced and evaluated in the same manner as in Example 1 except that the plasticizer used in the above was changed to dibutoxyethyl adipate. The results are shown in Tables 14 and 15.

Example 13
[Production of Layer (X)]
50 parts by mass of the synthesized PVB-1 powder, 19 parts by mass of triethylene glycol di-2-ethylhexanoate as a plasticizer, and 0.175 parts by mass of “Tinuvin 328” manufactured by Ciba Japan as an ultraviolet absorber Was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using a lab plast mill “C model” manufactured by Toyo Seiki Seisakusho Co., Ltd. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 310 μm.

[Preparation of layer (Y)]
A ZnSb ₂ O ₆ anhydrous zinc antimonate methanol dispersion (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill to prepare a zinc antimonate methanol dispersion having a concentration of 60% by mass. . 1.62 parts by mass of the obtained dispersion, 0.24 parts by mass of “DISPERBYK-102” manufactured by BYK Chemie as a phosphate ester, and 14.3 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer The dispersion obtained in this way, 14.4 parts by mass of triethylene glycol-di-2-ethylhexanoate, a 25% by mass aqueous solution 0.10 of a mixture of magnesium acetate and potassium acetate (mixing mass ratio: 2/1) 0.10 Mass parts and 43 parts by mass of the synthesized PVB-16 powder were melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using the Laboplast mill. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 140 μm.

[Production of laminated film]
Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 μm under conditions of 135 ° C. and 10 kg / cm ^2. A laminated film consisting of (X) (310 μm) / layer (Y) (140 μm) / layer (X) (310 μm) was obtained.

Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, except having used the obtained laminated | multilayer film as a recovered material, it carried out similarly to Example 1, and produced the single layer and the multilayer film which used the recovered material, and evaluated each. The results are shown in Tables 16 and 17.

Comparative Examples 10-13
Each film in the same manner as in Example 13 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 16 and 17, respectively. Were prepared and evaluated. The results are shown in Tables 16 and 17.

Example 14
[Production of Layer (X)]
50 parts by mass of the synthesized PVB-1 powder, 19 parts by mass of triethylene glycol di-2-ethylhexanoate as a plasticizer, and 0.175 parts by mass of “Tinuvin 328” manufactured by Ciba Japan as an ultraviolet absorber Was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using a lab plast mill “C model” manufactured by Toyo Seiki Seisakusho Co., Ltd. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 300 μm.

[Preparation of layer (Y)]
A ZnSb ₂ O ₆ anhydrous zinc antimonate methanol dispersion (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill to prepare a zinc antimonate methanol dispersion having a concentration of 60% by mass. . 1.62 parts by mass of the obtained dispersion, 0.24 parts by mass of “DISPERBYK-102” manufactured by BYK Chemie as a phosphate ester, and 21 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer were mixed. The obtained dispersion, 22 parts by mass of triethylene glycol-di-2-ethylhexanoate, 0.10 parts by mass of a 25% by mass aqueous solution of a mixture of magnesium acetate and potassium acetate (mixing mass ratio: 2/1), and 43 parts by mass of the synthesized PVB-17 powder was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using the Laboplast mill. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 160 μm.

[Production of laminated film]
Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 μm under conditions of 135 ° C. and 10 kg / cm ^2. A laminated film consisting of (X) (300 μm) / layer (Y) (160 μm) / layer (X) (300 μm) was obtained.

Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, except having used the obtained laminated | multilayer film as a collection | recovery thing, and having changed the quantity of the PVB newly added and the quantity of a plasticizer as shown in Table 18 and 19, similarly to Example 1, Single layer and multilayer films using the recovered material were prepared and evaluated. The results are shown in Tables 18 and 19.

Comparative Examples 14-17
Each film in the same manner as in Example 14 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 18 and 19, respectively. Were prepared and evaluated. The results are shown in Tables 18 and 19.

Example 15
[Production of Layer (X)]
46 parts by mass of the synthesized PVB-9 powder, 23 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer, and 0.175 parts by mass of “Tinuvin 328” manufactured by Ciba Japan as an ultraviolet absorber. Was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using a lab plast mill “C model” manufactured by Toyo Seiki Seisakusho Co., Ltd. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 320 μm.

[Preparation of layer (Y)]
A ZnSb ₂ O ₆ anhydrous zinc antimonate methanol dispersion (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill to prepare a zinc antimonate methanol dispersion having a concentration of 60% by mass. . 1.62 parts by mass of the obtained dispersion, 0.24 parts by mass of “DISPERBYK-102” manufactured by BYK Chemie as a phosphate ester, and 14.3 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer The dispersion obtained in this way, 14.4 parts by mass of triethylene glycol-di-2-ethylhexanoate, a 25% by mass aqueous solution 0.10 of a mixture of magnesium acetate and potassium acetate (mixing mass ratio: 2/1) 0.10 Mass parts and 43 parts by mass of the synthesized PVB-16 powder were melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using the Laboplast mill. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 120 μm.

[Production of laminated film]
Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 μm under conditions of 135 ° C. and 10 kg / cm ^2. A laminated film consisting of (X) (320 μm) / layer (Y) (120 μm) / layer (X) (320 μm) was obtained.

Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, it was the same as Example 1 except having used the obtained laminated | multilayer film as a collection | recovery, and having changed the kind and quantity of PVB to add newly, and the quantity of a plasticizer as shown in Table 20 and 21. Thus, single-layer and multilayer films using the recovered material were prepared and evaluated. The results are shown in Tables 20 and 21.

Comparative Examples 18-21
Each film in the same manner as in Example 15 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 20 and 21, respectively. Were prepared and evaluated. The results are shown in Tables 20 and 21.

Example 16
[Production of Layer (X)]
46 parts by mass of the synthesized PVB-9 powder, 23 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer, and 0.175 parts by mass of “Tinuvin 328” manufactured by Ciba Japan as an ultraviolet absorber. Was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using a lab plast mill “C model” manufactured by Toyo Seiki Seisakusho Co., Ltd. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 310 μm.

[Preparation of layer (Y)]
A ZnSb ₂ O ₆ anhydrous zinc antimonate methanol dispersion (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill to prepare a zinc antimonate methanol dispersion having a concentration of 60% by mass. . 1.62 parts by mass of the obtained dispersion, 0.24 parts by mass of “DISPERBYK-102” manufactured by BYK Chemie as a phosphate ester, and 21 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer were mixed. The obtained dispersion, 21 parts by mass of triethylene glycol-di-2-ethylhexanoate, 0.10 parts by mass of a 25% by mass aqueous solution of a mixture of magnesium acetate and potassium acetate (mixing mass ratio: 2/1), and 43 parts by mass of the synthesized PVB-17 powder was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using the Laboplast mill. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 140 μm.

Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, it was the same as that of Example 1 except having used the obtained laminated | multilayer film as a collection | recovery, and having changed the kind and quantity of PVB to add newly, and the quantity of a plasticizer as shown in Table 22 and 23. Thus, single-layer and multilayer films using the recovered material were prepared and evaluated. The results are shown in Tables 22 and 23.

Comparative Examples 22-25
Each film in the same manner as in Example 16 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 22 and 23, respectively. Were prepared and evaluated. The results are shown in Tables 22 and 23.

Example 17
[Production of Layer (X)]
40.6 parts by mass of the synthesized PVB-10 powder, 28.4 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer, and “Tinuvin 328” manufactured by Ciba Japan Co., Ltd. as an ultraviolet absorber are set to 0.0. 175 parts by mass was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using a lab plast mill “C model” manufactured by Toyo Seiki Co., Ltd. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 320 μm.

[Preparation of layer (Y)]
A ZnSb ₂ O ₆ anhydrous zinc antimonate methanol dispersion (“CX-Z693M-F” manufactured by Nissan Chemical Co., Ltd.) was pulverized with a bead mill to prepare a zinc antimonate methanol dispersion having a concentration of 60% by mass. . 1.62 parts by mass of the obtained dispersion, 0.24 parts by mass of “DISPERBYK-102” manufactured by BYK Chemie as a phosphate ester, and 21 parts by mass of triethylene glycol-di-2-ethylhexanoate as a plasticizer were mixed. The obtained dispersion, 21 parts by mass of triethylene glycol-di-2-ethylhexanoate, 0.10 parts by mass of a 25% by mass aqueous solution of a mixture of magnesium acetate and potassium acetate (mixing mass ratio: 2/1), and 43 parts by mass of the synthesized PVB-17 powder was melt-kneaded for 5 minutes at 170 ° C. and 50 rpm using the Laboplast mill. During melt kneading, nitrogen (100 mL / min) was continuously blown into the container. The obtained kneaded material was hot-pressed at 150 ° C. and 5 MPa for 30 minutes to produce a film having a thickness of 120 μm.

Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, it was the same as that of Example 1 except having used the obtained laminated | multilayer film as a collection | recovery, and having changed the kind and quantity of PVB to add newly, and the quantity of a plasticizer as shown in Table 24 and 25. Thus, single-layer and multilayer films using the recovered material were prepared and evaluated. The results are shown in Tables 24 and 25.

Comparative Examples 26-29
Each film in the same manner as in Example 17 except that the PVB used for the production of the layer (X), the PVB used for the production of the layer (Y), and the PVB added to the recovered material were changed to those shown in Tables 24 and 25, respectively. Were prepared and evaluated. The results are shown in Tables 24 and 25.

In the above examples, it is shown that the multilayer film of the present invention has sufficient heat shielding properties, little coloring due to heating, and few foreign matters (undissolved content). And the film using the collection | recovery of the said multilayer film is also shown that there is little coloring, there are few foreign materials (undissolved part), and it has the outstanding transparency.

Claims

Polyvinyl acetal (I) having an acetalization degree of 55 to 80 mol%, a vinyl ester monomer unit content of 0.1 to 1.5 mol% and a viscosity average polymerization degree of 1400 to 5000, UV absorption A layer (X) containing an agent and a plasticizer;
Polyvinyl acetal (II) having an acetalization degree of 70 to 85 mol%, a vinyl ester monomer unit content of 5 to 15 mol% and a viscosity average polymerization degree of 1400 to 5000, heat ray shielding fine particles, surface activity A layer (Y) containing an agent, an alkali metal salt and / or an alkaline earth metal salt, and a plasticizer,
A multilayer film in which the layer (X) is disposed on both outer sides of the layer (Y) and satisfies the following formulas (1) and (2).
(AB) / A <0.80 (1)
1.00 × 10 −2 <(b / y) / (a / x) <2.00 × 10 −1 (2)
Where
A: When the multilayer film heated at 230 ° C. for 3 hours is measured by gel permeation chromatography, the peak top molecular weight of the polymer component measured by the differential refractive index detector a: the signal at the peak top molecular weight (A) Intensity B: peak top molecular weight of polymer component measured with an absorptiometric detector (measurement wavelength: 280 nm) when the multilayer film heated at 230 ° C. for 3 hours is measured by gel permeation chromatography b: peak top molecular weight Signal intensity x in (B): Signal intensity at peak top molecular weight measured by differential refractive index detector when monodisperse polymethyl methacrylate is measured by gel permeation chromatography y: Monodisperse polymethacrylic acid Methyl gel permeation Upon chromatographic measurement, a signal intensity at the peak top molecular weight measured by spectrophotometric detector (measuring wavelength 220 nm).
The multilayer film of Claim 1 which satisfy | fills following formula (3) and (4).
(AC) / A <0.80 (3)
5.00 × 10 −3 <(c / y) / (a / x) <7.00 × 10 −2 (4)
Where
A: Same as the formula (1), a, x, y: Same as the formula (2) C: Absorbance detection when the multilayer film heated at 230 ° C. for 3 hours is measured by gel permeation chromatography The peak top molecular weight c of the polymer component measured with a vessel (measurement wavelength: 320 nm): the signal intensity at the peak top molecular weight (C).
The multilayer film according to claim 1 or 2, wherein the polyvinyl acetal (I) and the polyvinyl acetal (II) are polyvinyl butyral.
An interlayer film for laminated glass comprising the multilayer film according to any one of claims 1 to 3.
Laminated glass obtained by bonding a plurality of glass plates using the interlayer film for laminated glass according to claim 4.
A method for producing a single layer film, wherein the recovered product of the multilayer film according to any one of claims 1 to 3 is melt-kneaded and then formed.
The recovered product, polyvinyl acetal (III) having a degree of acetalization of 55 to 85 mol%, a content of vinyl ester monomer units of 0.1 to 15 mol% and a viscosity average polymerization degree of 1400 to 5000, The method for producing a single layer film according to claim 6, wherein the film is formed after melt-kneading the plasticizer.
The recovered multilayer film according to any one of claims 1 to 3, wherein the degree of acetalization is 55 to 85 mol%, the content of vinyl ester monomer units is 0.1 to 15 mol%, and the viscosity average A layer formed by melt-kneading a polyvinyl acetal (III) having a polymerization degree of 1400 to 5000, a plasticizer, a heat ray shielding fine particle, a surfactant, and an alkali metal salt and / or alkaline earth metal salt ( On both outer sides of Y ′)
The manufacturing method of the multilayer film which arrange | positions layer (X) formed by melt-kneading polyvinyl acetal (I), a ultraviolet absorber, and a plasticizer, and forming into a film.