WO2015059831A1 - Film multicouches et film intermédiaire pour verre stratifié formé de ceux-ci - Google Patents

Film multicouches et film intermédiaire pour verre stratifié formé de ceux-ci Download PDF

Info

Publication number
WO2015059831A1
WO2015059831A1 PCT/JP2013/079023 JP2013079023W WO2015059831A1 WO 2015059831 A1 WO2015059831 A1 WO 2015059831A1 JP 2013079023 W JP2013079023 W JP 2013079023W WO 2015059831 A1 WO2015059831 A1 WO 2015059831A1
Authority
WO
WIPO (PCT)
Prior art keywords
film
layer
multilayer film
mass
polyvinyl acetal
Prior art date
Application number
PCT/JP2013/079023
Other languages
English (en)
Japanese (ja)
Inventor
楠藤　健
太我 油井
Original Assignee
株式会社クラレ
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 株式会社クラレ filed Critical 株式会社クラレ
Priority to JP2013549649A priority Critical patent/JP5469287B1/ja
Priority to PCT/JP2013/079023 priority patent/WO2015059831A1/fr
Publication of WO2015059831A1 publication Critical patent/WO2015059831A1/fr

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/14—Homopolymers or copolymers of acetals or ketals obtained by polymerisation of unsaturated acetals or ketals or by after-treatment of polymers of unsaturated alcohols
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10614—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer comprising particles for purposes other than dyeing
    • B32B17/10633—Infrared radiation absorbing or reflecting agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10678—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer comprising UV absorbers or stabilizers, e.g. antioxidants
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10688—Adjustment of the adherence to the glass layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10761—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing vinyl acetal
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/03—3 layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2305/00—Condition, form or state of the layers or laminate
    • B32B2305/70—Scrap or recycled material
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure

Definitions

  • 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.
  • PVA polyvinyl alcohol
  • 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.
  • polyvinyl butyral is widely used as an interlayer film for laminated glass of automobiles and buildings, and occupies a particularly important position commercially.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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).
  • 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.
  • 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.
  • 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.
  • 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.
  • 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 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).
  • GPC gel permeation chromatography
  • 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.
  • 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).
  • hexafluoroisopropanol may be abbreviated as HFIP.
  • Sample concentration 1.00 mg / ml
  • Sample injection volume 100 ⁇ l
  • Column temperature 40 ° C
  • Flow rate 1.0 ml / min.
  • the multilayer film satisfies the following formulas (3) and (4).
  • 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.
  • 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.
  • 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).
  • RI differential refractive index detector
  • UV absorptiometric detector
  • 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.
  • the layer (X) is disposed on both outer sides of the layer (Y) and satisfies the following formulas (1) and (2).
  • the peak top molecular weight b of the polymer component measured by an absorptiometric detector 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.
  • a GPC apparatus having a differential refractive index detector and an absorptiometric detector and capable of simultaneously performing measurement by these detectors.
  • 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.
  • the components detected by the absorptiometric detector are only those having a structure that absorbs a predetermined wavelength.
  • 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.
  • “GPC HFIP-806M” manufactured by Showa Denko KK is preferably used.
  • standard PMMA is monodispersed 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.
  • 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.
  • the multilayer film is heated at 230 ° C. for 3 hours.
  • 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.
  • the thickness of the film to be heated is 600 to 800 ⁇ m, preferably about 760 ⁇ m, 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 ⁇ l.
  • 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 ⁇ l) 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.
  • 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.
  • 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
  • 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.
  • the peak seen in the molecular weight 1500 vicinity is a peak of the plasticizer contained in a film.
  • the molecular weight at the peak position having the highest peak height is defined as the peak top molecular weight (A).
  • 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.
  • 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
  • the signal intensity (absorbance) at the peak top molecular weight (B) is defined as the signal intensity (b).
  • the peak top molecular weight (B) of the polymer component usually exceeds 3500.
  • 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.
  • the peak top molecular weight (B) is derived from a component having absorption at 280 nm, which is present in the polymer component.
  • (AB) / A becomes a positive value.
  • the low molecular weight component contains more components that absorb ultraviolet light having a wavelength of 280 nm.
  • the foreign matter (undissolved part) in the obtained multilayer film increases.
  • 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)
  • 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).
  • 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).
  • 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.
  • the signal intensity by the differential refractive index detector is approximately proportional to the concentration (g / l) of the film component.
  • 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. .
  • the signal intensity of the differential refractive index detector is indicated by “millivolt”
  • the signal intensity (absorbance) of the absorptiometric detector is indicated by “absorbance unit (AU)”.
  • the ratio of both is simply compared. It ’s difficult.
  • 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.
  • 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
  • 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 ′′)
  • 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
  • the peak top molecular weight (A) measured with a differential refractive index detector in the GPC measurement 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.
  • (AC) / A becomes a positive value.
  • the low molecular weight component contains more components that absorb ultraviolet rays having a wavelength of 320 nm.
  • foreign matter undissolved content
  • 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)
  • 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).
  • (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
  • 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 ")
  • 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.
  • recovery of a multilayer film may also increase, and there exists a possibility that the transparency of the said film may fall.
  • 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
  • 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 [ ⁇ ] 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 ([ ⁇ ] ⁇ 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.
  • the viscosity average degree of polymerization is less than 1400, the strength of the multilayer film is insufficient.
  • 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
  • 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.
  • 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.
  • the degree of acetalization represents the ratio of acetalized vinyl alcohol monomer units to the total monomer units constituting polyvinyl acetal.
  • 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%.
  • 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.
  • 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%.
  • the resulting multilayer film is colored by heating.
  • 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.
  • the content of the vinyl ester monomer unit is preferably 6 mol% or more, more preferably 7 mol% or more.
  • 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%.
  • 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 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%.
  • 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.
  • 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.
  • 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.
  • 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.
  • vinyl acid examples 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.
  • thiol compounds such as 2-mercaptoethanol, n-dodecyl mercaptan, mercaptoacetic acid, 3-mercaptopropionic acid
  • Examples of the method for polymerizing the vinyl ester monomer include known methods such as bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization.
  • a bulk polymerization method performed without a solvent or a solution polymerization method performed using a solvent such as alcohol is usually employed.
  • 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.
  • the reaction can be carried out by either a batch method or a continuous method.
  • 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.
  • an organic oxide initiator having a half-life of 10 to 110 minutes at 60 ° C. is preferable, and peroxydicarbonate is particularly preferable.
  • the polymerization temperature for carrying out the polymerization reaction but a range of 5 ° C to 200 ° C is suitable.
  • a copolymerizable monomer can be copolymerized as necessary as long as the effects of the present invention are not impaired.
  • monomers include ⁇ -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-ethy
  • 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.
  • 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.
  • 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.
  • the raw material PVA preferably contains a predetermined amount of an alkali metal salt of carboxylic acid.
  • 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.
  • cleaning liquid may contain ester, such as methyl acetate produced
  • 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.
  • 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.
  • 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.
  • PVA welled gel
  • a washing solution 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.
  • 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,
  • 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
  • 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 reti
  • the PVA thus obtained is acetalized to produce polyvinyl acetal used for film production.
  • 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.
  • 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.
  • polyvinyl acetal having reached a certain degree of acetalization is precipitated.
  • the temperature of the reaction solution is raised to 25 to 80 ° C.
  • aggregated particles made of polyvinyl acetal are generated in such a reaction or processing step, and coarse particles are easily formed.
  • coarse particles are generated, there is a risk of causing variation between batches.
  • 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.
  • 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.
  • the PVA of the present invention when 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.
  • polyvinyl acetal obtained by using two or more aldehydes in combination can also be used.
  • 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.
  • phenolic antioxidants examples 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
  • phosphorus antioxidants include triphenyl phosphite, diphenylisodecyl phosphite, phenyl diisodecyl phosphite, tris (nonylphenyl) phosphite, tris (dinonylphenyl) phosphite, tris (2-t-butyl).
  • sulfur-based antioxidant examples include dilauryl 3,3′-thiodipropionate, distearyl 3,3′-thiodipropionate, lauryl stearyl 3,3′-thiodipropionate, pentaerythritol-tetrakis- ( ⁇ -lauryl-thiopropionate), 3,9-bis (2-dodecylthioethyl) -2,4,8,10-tetraoxaspiro [5.5] undecane.
  • 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.
  • 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.
  • 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.
  • 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.
  • the impurities contained in the solvent include those described above as the impurities contained in the raw material vinyl ester monomer.
  • 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.
  • an inhibitor 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.
  • 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.
  • 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-
  • 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.
  • a polyvinyl ester alcohol solution from which the remaining vinyl ester monomer is removed as much as possible is used for the saponification reaction.
  • 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.
  • 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.
  • aliphatic carboxylic acid examples 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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
  • 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.
  • polyester compound having a hydroxyl group examples 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 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
  • a hydroxyl group examples include an aliphatic polycarbonate polyol 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
  • 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. .
  • aliphatic polycarboxylic acids examples 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.
  • An aliphatic polyester having a hydroxyl group which is a polymer of hydroxycarboxylic acid, can be obtained by condensation polymerization of hydroxycarboxylic acid.
  • 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.
  • lactone compound examples include, but are not limited to, ⁇ -butyrolactone, ⁇ -valerolactone, ⁇ -caprolactone, 4-methyl- ⁇ -valerolactone, and the like.
  • a lactone compound When a lactone compound is used, a polyester can be obtained by ring-opening polymerization. Of these, 6-hydroxycarboxylic acid or ⁇ -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.
  • 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.
  • the compatibility between the compound and polyvinyl acetal may be insufficient.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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
  • 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
  • ether compounds with alkylene glycols such as polyoxyethylene naphthyl ether
  • these ether compounds are preferably monoethers.
  • a compound etherified with a plurality of polyethylene glycols such as 2,2-bis (4-polyoxyethyleneoxyphenyl) propane may be mentioned.
  • 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.
  • polyoxyethylene alkylphenyl ether an ether compound of an aromatic alcohol having a plurality of aromatic rings and polyoxyethylene
  • 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.
  • 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.
  • 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 ( ⁇ , ⁇ '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-t
  • 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.
  • 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.
  • 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.
  • 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.
  • the temperature is in the range of 5 to 45 ° C, more preferably 10 to 40 ° C.
  • 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.
  • 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.
  • a surfactant as a dispersant for the heat ray shielding fine particles.
  • 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.
  • 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
  • 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.
  • 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
  • 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.
  • the glass transition temperature is preferably in the above range.
  • 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.
  • 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
  • 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.
  • 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.
  • 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.
  • 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.
  • 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, ⁇ -butyrolactone, ⁇ -caprolactone, N -Methylpyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, hexane, toluene, acetonitrile and the like.
  • 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.
  • 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.
  • the forming method the method described above as the melt forming method used for the production of the layer (X) is used.
  • 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.
  • 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.
  • the thickness exceeds 1 mm the mechanical strength of the multilayer film cannot be expected by increasing the thickness.
  • 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).
  • 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.
  • 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
  • An interlayer film for laminated glass comprising the multilayer film of the present invention is a preferred embodiment of the present invention.
  • an adhesiveness adjusting agent may be contained in the layer (X).
  • 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.
  • 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%.
  • 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 ⁇ m to 500 ⁇ m, more preferably 7 ⁇ m to 300 ⁇ m, and still more preferably 10 ⁇ m to 200 ⁇ m. When the embossing height is less than 5 ⁇ m, bubbles formed between the glass and the intermediate film may not be efficiently removed when laminating to glass, and when it exceeds 500 ⁇ m, it is difficult to form embossing. Moreover, although embossing may be given to the single side
  • 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.
  • the embossing roll method 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.
  • 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.
  • the embossing roll used in the embossing roll method is preferably subjected to a release treatment.
  • a roll without mold 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the viscosity average degree of polymerization is less than 1400, the strength of the obtained multilayer film is insufficient.
  • 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%.
  • the degree of acetalization is preferably 60 mol% or more, more preferably 65 mol% or more.
  • 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.
  • 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).
  • 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).
  • 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.
  • a measuring machine such as a gear pump
  • a die such as a T die.
  • trims 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.
  • 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.
  • the formation of coarse particles is suppressed during the acetalization reaction, and as a result, the resulting polyvinyl acetal is melt-formed.
  • a film with reduced foreign matter (undissolved content) can be obtained.
  • 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.
  • plasticizer newly added to the recovered material those described above as used in the production of the layer (X) are used.
  • plasticizer to be newly added any of the aforementioned plasticizers can be used as long as the resulting single layer film has excellent transparency.
  • 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.
  • 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.
  • 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.
  • the method described above as the method used when producing the layer (X) is used.
  • 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.
  • 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.
  • 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.
  • the haze of the laminated glass thus obtained is 1.0 or less.
  • the haze of the laminated glass is measured according to JIS K7105.
  • 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.
  • polyvinyl acetal (III) those described above as being used for a monolayer film obtained using the recovered material are used.
  • 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).
  • 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.
  • 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.
  • the recovered material is 1 to 10000 parts by mass with respect to 100 parts by mass of polyvinyl acetal (III).
  • 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.
  • 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.
  • 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
  • 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
  • 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).
  • 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.
  • 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.
  • 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.
  • 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.
  • “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.
  • 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.
  • 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).
  • 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.
  • 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.
  • 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.
  • 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.
  • the composition of the obtained PVB was measured in the same manner as PVB-1.
  • the degree of butyralization degree of acetalization
  • the degree of acetalization was 68.1 mol%
  • the content of vinyl acetate monomer units was 1.5 mol%
  • the content of vinyl alcohol monomer units was 30.4 mol%. It was.
  • 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.
  • the composition of the obtained PVB was measured in the same manner as PVB-1.
  • the degree of butyralization degree of acetalization
  • the degree of acetalization was 74.1 mol%
  • the content of vinyl acetate monomer units was 8.1 mol%
  • 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.
  • the composition of the obtained PVB was measured in the same manner as PVB-1.
  • the degree of butyralization degree of acetalization
  • the degree of acetalization was 74.6 mol%
  • the content of vinyl acetate monomer units was 8.3 mol%
  • 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.
  • 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%
  • 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 ⁇ m.
  • Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 ⁇ m under conditions of 135 ° C. and 10 kg / cm 2.
  • a multilayer film composed of (X) (320 ⁇ m) / layer (Y) (120 ⁇ m) / layer (X) (320 ⁇ m) 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.
  • HFIP HFIP containing 20 mmol / l sodium trifluoroacetate was used as the mobile phase.
  • the mobile phase flow rate was 1.0 ml / min.
  • the sample injection amount was 100 ⁇ l, and measurement was performed at a GPC column temperature of 40 ° C.
  • 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. ⁇ (mg / ml) is the concentration of the diluted sample.
  • Absorbance at a sample concentration of 1.00 mg / ml (1.00 / ⁇ ) ⁇ measured value of absorbance
  • the signal intensity obtained from the differential refractive index detector is expressed in millivolts
  • the signal intensity obtained from the absorptiometric detector is expressed in absorbance (abs unit: Absorbance unit).
  • 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.
  • 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 ⁇ m polytetrafluoroethylene filter and then subjected to GPC measurement.
  • 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.
  • 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.
  • PMMA85K weight average molecular weight 85450, number average molecular weight 74300, intrinsic viscosity 0.309
  • 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 (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 (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.
  • 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 ⁇ m.
  • the laminated film obtained in the above “production of laminated film” was cut into a size of 1 cm ⁇ 1 cm.
  • 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
  • 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 ⁇ m. This was designated as a layer (Y ′).
  • a laminated film consisting of the layer (X) (320 ⁇ m) was obtained.
  • 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.
  • 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.
  • ITO isopropanol dispersion manufactured by Mitsubishi Materials Corporation
  • 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 ⁇ m.
  • Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 ⁇ m under conditions of 135 ° C. and 10 kg / cm 2.
  • a laminated film consisting of (X) (310 ⁇ m) / layer (Y) (140 ⁇ m) / layer (X) (310 ⁇ m) was obtained.
  • Example 2 Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, except having used the obtained laminated
  • 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 ⁇ m.
  • 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 ⁇ m.
  • Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 ⁇ m under conditions of 135 ° C. and 10 kg / cm 2.
  • a laminated film consisting of (X) (300 ⁇ m) / layer (Y) (160 ⁇ m) / layer (X) (300 ⁇ m) was obtained.
  • Example 2 Evaluation of the obtained laminated film was evaluated in the same manner as in Example 1. Moreover, except having used the obtained laminated
  • 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.
  • Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 ⁇ m under conditions of 135 ° C. and 10 kg / cm 2.
  • a laminated film consisting of (X) (320 ⁇ m) / layer (Y) (120 ⁇ m) / layer (X) (320 ⁇ m) was obtained.
  • Example 1 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
  • 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.
  • 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 ⁇ m.
  • Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 ⁇ m under conditions of 135 ° C. and 10 kg / cm 2.
  • a laminated film consisting of (X) (310 ⁇ m) / layer (Y) (140 ⁇ m) / layer (X) (310 ⁇ m) was obtained.
  • Example 2 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
  • 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 ⁇ m.
  • 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 ⁇ m.
  • Layer (X) and layer (Y) are layered in the order of layer (X) / layer (Y) / layer (X), and pressed in a form of 760 ⁇ m under conditions of 135 ° C. and 10 kg / cm 2.
  • a laminated film consisting of (X) (320 ⁇ m) / layer (Y) (120 ⁇ m) / layer (X) (320 ⁇ m) was obtained.
  • Example 1 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
  • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Joining Of Glass To Other Materials (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

L'invention concerne un film multicouches qui comprend une couche (X) qui contient un acétal de polyvinyle (I) présentant un degré d'acétalisation de 55-80% par mole, une teneur en une unité de monomère d'ester vinylique de 0,1-1,5% par mole et un degré de polymérisation de viscosité moyenne de 1400-5000, un agent absorbant les ultraviolets et un plastifiant, et une couche (Y) qui contient un acétal de polyvinyle (II) présentant un degré d'acétalisation de 70-85% par mole, une teneur en une unité de monomère d'ester vinylique de 5-15% par mole et un degré de polymérisation à viscosité moyenne de 1400-5000, des particules fines bloquant la chaleur, un tensioactif, un sel métallique alcalin et/ou un sel métallique terreux alcalin et un plastifiant, la couche (X) étant agencée sur les deux surfaces externes de la couche (Y). Ce film multicouches satisfait les formules (1) et (2). (A - B) /A < 0,80 (1) 1,00 x 10-2 < (b/y)/(a/x) < 2,00 x 10-1 (2) Par conséquent, un film qui présente une performance de blocage de la chaleur suffisante, une performance d'absorption acoustique suffisante, une inclusion réduite de substances étrangères (contenus non dissous) et une excellente recyclabilité tout en supprimant la coloration provoquée par le chauffage peut être fourni.
PCT/JP2013/079023 2013-10-25 2013-10-25 Film multicouches et film intermédiaire pour verre stratifié formé de ceux-ci WO2015059831A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2013549649A JP5469287B1 (ja) 2013-10-25 2013-10-25 複層フィルム及びそれからなる合わせガラス用中間膜
PCT/JP2013/079023 WO2015059831A1 (fr) 2013-10-25 2013-10-25 Film multicouches et film intermédiaire pour verre stratifié formé de ceux-ci

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2013/079023 WO2015059831A1 (fr) 2013-10-25 2013-10-25 Film multicouches et film intermédiaire pour verre stratifié formé de ceux-ci

Publications (1)

Publication Number Publication Date
WO2015059831A1 true WO2015059831A1 (fr) 2015-04-30

Family

ID=50749746

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2013/079023 WO2015059831A1 (fr) 2013-10-25 2013-10-25 Film multicouches et film intermédiaire pour verre stratifié formé de ceux-ci

Country Status (2)

Country Link
JP (1) JP5469287B1 (fr)
WO (1) WO2015059831A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019094257A (ja) * 2017-03-27 2019-06-20 株式会社クラレ 合わせガラス用のポリビニルアセタール樹脂フィルム
CN112409677A (zh) * 2020-10-12 2021-02-26 上海春宜药品包装材料有限公司 一种可降解复合膜及其制备方法
EP3636612A4 (fr) * 2017-06-08 2021-03-17 Kuraray Co., Ltd. Procédé de réutilisation de film intermédiaire pour verre feuilleté

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6441307B2 (ja) * 2014-02-18 2018-12-19 株式会社クラレ 合わせガラス用中間膜
JP6501498B2 (ja) * 2014-11-07 2019-04-17 マークテック株式会社 ゴム用塗料
CN107108351A (zh) * 2014-11-10 2017-08-29 株式会社可乐丽 夹层玻璃用中间膜和夹层玻璃

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003252655A (ja) * 2002-02-27 2003-09-10 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2004002108A (ja) * 2002-05-31 2004-01-08 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2011508802A (ja) * 2007-12-21 2011-03-17 セキスイ・スペシャルティ・ケミカルズ・アメリカ・エルエルシー 低色ポリビニルアルコールの作成方法
JP2011084468A (ja) * 2009-02-23 2011-04-28 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2011251906A (ja) * 2003-12-26 2011-12-15 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2012025645A (ja) * 2010-07-28 2012-02-09 Kuraray Co Ltd 合わせガラス用中間膜、その製造方法およびそれを用いた合わせガラス

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003252655A (ja) * 2002-02-27 2003-09-10 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2004002108A (ja) * 2002-05-31 2004-01-08 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2011251906A (ja) * 2003-12-26 2011-12-15 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2011508802A (ja) * 2007-12-21 2011-03-17 セキスイ・スペシャルティ・ケミカルズ・アメリカ・エルエルシー 低色ポリビニルアルコールの作成方法
JP2011084468A (ja) * 2009-02-23 2011-04-28 Sekisui Chem Co Ltd 合わせガラス用中間膜及び合わせガラス
JP2012025645A (ja) * 2010-07-28 2012-02-09 Kuraray Co Ltd 合わせガラス用中間膜、その製造方法およびそれを用いた合わせガラス

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019094257A (ja) * 2017-03-27 2019-06-20 株式会社クラレ 合わせガラス用のポリビニルアセタール樹脂フィルム
JP7046789B2 (ja) 2017-03-27 2022-04-04 クラレイ ユーロップ ゲゼルシャフト ミット ベシュレンクテル ハフツング 合わせガラス用のポリビニルアセタール樹脂フィルム
EP3636612A4 (fr) * 2017-06-08 2021-03-17 Kuraray Co., Ltd. Procédé de réutilisation de film intermédiaire pour verre feuilleté
US11518147B2 (en) 2017-06-08 2022-12-06 Kuraray Europe Gmbh Method for recycling intermediate film for laminated glass
CN112409677A (zh) * 2020-10-12 2021-02-26 上海春宜药品包装材料有限公司 一种可降解复合膜及其制备方法

Also Published As

Publication number Publication date
JP5469287B1 (ja) 2014-04-16
JPWO2015059831A1 (ja) 2017-03-09

Similar Documents

Publication Publication Date Title
JP5469286B1 (ja) 複層フィルム及びそれからなる合わせガラス用中間膜
JP5632077B1 (ja) 透明性に優れる組成物
JP5469287B1 (ja) 複層フィルム及びそれからなる合わせガラス用中間膜
JP6441307B2 (ja) 合わせガラス用中間膜
JP5420804B1 (ja) ポリビニルアセタールを含有するフィルム
JP5529345B1 (ja) ポリビニルアセタール組成物
JP5420808B1 (ja) ポリビニルアセタールを含有するフィルム
JP5469288B1 (ja) 複層フィルム及びそれからなる合わせガラス用中間膜
JP6259307B2 (ja) 合わせガラス用中間膜およびそれを用いた合わせガラス
JP5469289B1 (ja) 複層フィルム及びそれからなる合わせガラス用中間膜
JP2012530034A (ja) ヘイズの低い、赤外線吸収性の合わせガラス用中間膜
JP5420806B1 (ja) ポリビニルアセタール及びそれを含有する合わせガラス用中間膜
JP5420805B1 (ja) ポリビニルアセタールおよびそれを含有する合わせガラス用中間膜

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 2013549649

Country of ref document: JP

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13896054

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 13896054

Country of ref document: EP

Kind code of ref document: A1