WO1998044026A1 - Films de resine fluoree, stratifies obtenus a partir dudit materiau, et procede de production desdits stratifies - Google Patents
Films de resine fluoree, stratifies obtenus a partir dudit materiau, et procede de production desdits stratifies Download PDFInfo
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- WO1998044026A1 WO1998044026A1 PCT/JP1998/001397 JP9801397W WO9844026A1 WO 1998044026 A1 WO1998044026 A1 WO 1998044026A1 JP 9801397 W JP9801397 W JP 9801397W WO 9844026 A1 WO9844026 A1 WO 9844026A1
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- film
- adhesive
- tetrafluoroethylene
- laminate
- ethylene copolymer
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- 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
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/085—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
- B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
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- 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
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- 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
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
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- 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
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- 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
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
- B32B27/322—Layered products comprising a layer of synthetic resin comprising polyolefins comprising halogenated polyolefins, e.g. PTFE
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- 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
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B38/0008—Electrical discharge treatment, e.g. corona, plasma treatment; wave energy or particle radiation
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- 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
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2027/00—Use of polyvinylhalogenides or derivatives thereof as moulding material
- B29K2027/12—Use of polyvinylhalogenides or derivatives thereof as moulding material containing fluorine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2027/00—Use of polyvinylhalogenides or derivatives thereof as moulding material
- B29K2027/12—Use of polyvinylhalogenides or derivatives thereof as moulding material containing fluorine
- B29K2027/18—PTFE, i.e. polytetrafluorethene, e.g. ePTFE, i.e. expanded polytetrafluorethene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0085—Copolymers
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- 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
- B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
- B32B2309/02—Temperature
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- 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
- B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
- B32B2309/04—Time
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- 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
- B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
- B32B2309/12—Pressure
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- 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
- B32B2311/00—Metals, their alloys or their compounds
- B32B2311/24—Aluminium
-
- 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
- B32B2323/00—Polyalkenes
- B32B2323/04—Polyethylene
-
- 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
- B32B2327/00—Polyvinylhalogenides
- B32B2327/12—Polyvinylhalogenides containing fluorine
-
- 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
- B32B2327/00—Polyvinylhalogenides
- B32B2327/12—Polyvinylhalogenides containing fluorine
- B32B2327/18—PTFE, i.e. polytetrafluoroethylene
-
- 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
- B32B2419/00—Buildings or parts thereof
- B32B2419/06—Roofs, roof membranes
-
- 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
- B32B2471/00—Floor coverings
-
- 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
- B32B2607/00—Walls, panels
- B32B2607/02—Wall papers, wall coverings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use 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 a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Definitions
- Fluorine-based film laminate using the same, and method for producing laminate
- the present invention relates to a tetrafluoroethylene-ethylene copolymer (hereinafter, referred to as ETFE) film, a laminate using the same, and a method for producing a laminate.
- ETFE tetrafluoroethylene-ethylene copolymer
- Fluorine resins such as ETFE have excellent chemical resistance and stain resistance. Laminates made by laminating fluoroplastic films on substrates such as metals and plastics are widely used in flooring, copyboard, wallpaper, roofing, gas stove tops, gas range hoods, surface protection films, solar cell covers, etc. It is used for However, in order to bond a fluororesin film such as an ETFE film to various substrates with an adhesive, a surface treatment for physically and chemically modifying the fluororesin surface is required. This is to improve the wettability of the adhesive to a fluororesin having a low surface energy.
- a corona discharge treatment method As a surface treatment method, a corona discharge treatment method is generally known. Further, as an alternative to corona discharge treatment, RF sputtering under high vacuum and high power density conditions (see JP-A-51-125455) to improve adhesion, special atmosphere gas Among them, a method of performing RF sputtering (see Japanese Patent Application Laid-Open No. 6-285988) and a method of performing RF sputtering for a long time (see Japanese Patent Application Laid-Open No. 6-298971) have been proposed. However, the ETFE film surface-treated by any of these methods had insufficient adhesive strength for practical use.
- An object of the present invention is to provide an ETFE film exhibiting good adhesive strength, a laminate using the ETFE film, and a method for producing the laminate.
- the present invention relates to a surface-treated tetrafluoroethylene-ethylene-based copolymer film, wherein a polar group is present on the surface-treated film surface, and the surface-treated film surface Te trough Ruo Russia ethylene-E Ji alkylene copolymer film, wherein the surface roughness R a is less than the surface roughness R a of the untreated tetrafluoropropoxy O b ethylene one ethylene copolymer film surface provide.
- the present invention also relates to a surface-treated tetrafluoroethylene-ethylene copolymer film, wherein a polar group is present on the surface of the surface-treated film, and the surface-treated film is Aluminum sheet on the surface at 100 ° C, contact pressure 21
- the amount of fluorine atoms present on the surface of the aluminum sheet peeled after hot pressing at kg f / cm 2 for 10 minutes and cooling at room temperature was reduced on the surface of the untreated tetrafluoroethylene-ethylene copolymer film.
- a tetrafluoroethylene-ethylene copolymer (ETFE) film characterized in that the amount of fluorine atoms present on the surface of the aluminum sheet peeled off after cooling to room temperature after the hot pressing is 1 or less. .
- FIG. 1 is a graph showing the relationship between the adhesion between an ETFE film and an ethylene-vinyl acetate copolymer (EVA) film and the amount of fluorine transferred.
- EVA ethylene-vinyl acetate copolymer
- Fig. 2 is a graph showing the relationship between the adhesion between the ETFE film and the soft vinyl chloride film (hereinafter simply referred to as vinyl chloride) and the amount of fluorine transfer.
- FIG. 3 is a schematic cross-sectional view for explaining an example of an RF bombarding device used for surface treatment of the ETF E film of the present invention.
- FIG. 4 is a schematic cross-sectional view for explaining an example of a DC pombard device used for surface treatment of the ETF E film of the present invention.
- FIG. 5 is a diagram of the ESC A spectrum of the surface of the ETFE film subjected to the surface treatment according to the present invention.
- FIG. 6 is a diagram of the ESC A spectrum on the surface of the ETFE film subjected to the corona discharge treatment.
- FIG. 7 is a schematic perspective view for explaining an apparatus and a method for manufacturing a laminate of an ETFFE film and vinyl chloride.
- FIG. 8 is a schematic perspective view for explaining an apparatus and a method for manufacturing a laminate of an ETFE film and a stainless steel plate (hereinafter, simply referred to as a SUS plate).
- the present inventors have studied in detail the relationship between the surface state and the adhesive force of a surface-treated ETFE film, and as a result, the surface-treated ETFE film has a polar group on the surface-treated film surface. It has been found that an ETFE film that exists and has a small amount of a weak bonding layer adhered to the film surface with a weak bonding force exhibits extremely good adhesive strength.
- the weak bonding layer is mainly composed of oligomers formed by cutting the polymer.
- On fluororesin film surface such as ETFE film Has a weak binding layer (weak bound ary 1 ayer, hereafter referred to as WBL), and the presence of this WBL greatly affects the adhesiveness and adhesion.
- WBLs are only weakly adhered to the film substrate and hinder adhesion and adhesion, and a small amount of WBL gives excellent adhesion and adhesion. Was found necessary. Furthermore, it has been found that it is necessary to prevent the surface treatment from increasing, and desirably reduce, the amount of WBL present on the ETFE film surface prior to the surface treatment in order to provide excellent adhesion and adhesion. .
- a hydroxyl group and a carbonyl or carbonyl group are preferably present as polar groups in order to impart adhesiveness.
- an ETFFE film having a hydroxyl group and a carbonyl group on the surface can be easily obtained.
- the surface functional group of the surface-treated ETFE film can be identified by the ESCA (E1ctr0nSpectrofoscopyformChalica1Ana1ysis) method and a chemical modification method.
- ESCA E1ctr0nSpectrofoscopyformChalica1Ana1ysis
- the surface roughness of the surface-treated film surface is equal to or less than the surface roughness of the untreated ETFE film surface.
- ETFE films exhibit extremely good adhesion. It is preferable that the surface of the surface-treated ETFE film is in a state where there is no noticeable unevenness (a state in which cone-shaped projections are not formed). In particular, it is preferable that the crystal structure in the untreated state is not damaged after the surface treatment.
- the surface roughness in the present invention has an arithmetic mean surface roughness R a (hereinafter, simply referred to as R a) defined by JISB 0601 represented by represented by.
- R was measured in a non-contact operation dynamic mode using AFM (Atomic Source Microscoe).
- the R a of ET FE film of the present invention was measured using AFM.
- Ra was equal to or less than that of the untreated ETFE film.
- the ETFE film of the present invention having such R has excellent adhesive strength and adhesive strength. In particular, it was found that when Ra was 10 nm or less, excellent adhesion and adhesion were exhibited.
- the present invention also includes a substrate, and the surface-treated ETFE film provided by laminating (hereinafter, also referred to as a laminate) with the substrate with the surface-treated film surface facing the substrate. To provide a laminate.
- a laminating adhesive (hereinafter simply referred to as an adhesive) is further provided between the substrate and the tetrafluoroethylene-ethylene copolymer film, and the substrate and the tetrafluoroethylene-ethylene copolymer are further provided. It is preferable that the polymer film is adhered to the adhesive with the adhesive.
- ETFE film with WB L amount and R a be performed to a surface treatment of untreated ETFE film and these equivalents ETFE film by the following method is obtained, and However, it was found that the treated ETFE film had excellent adhesion.
- a preferable one is an RF bombardment treatment.
- RF high-frequency
- plasma of a rare gas is generated in the space between the electrodes.
- Plasma contains active species such as radical atoms and ions, which can physically and chemically change the state of the substrate surface by colliding with electrodes or a substrate placed in the plasma.
- the method of applying this effect to the modification of the surface state is called RF bombardment treatment.
- the bombardment treatment is a treatment characterized by adding a weak etching effect by gentle sputtering to a chemical surface modification effect by plasma.
- the processing state changes depending on the gas type, gas pressure, input power, distance between electrodes, substrate installation position, etc.
- a DC (direct current) bombardment treatment is preferably used as a surface treatment method for the ETFE film. This is a process in which the RF of the RF bombarding process is changed to DC, and the same effect can be obtained.
- DC bombardment treatment a DC voltage is applied between opposing electrodes to generate plasma, and this plasma is used to generate plasma. Changes the surface physically and chemically.
- the equipment is simpler than RF bombardment processing, so it is easy to increase the size and is suitable for mass production. However, some contrivance is required for equipment conditions.
- the input power is preferably from 0.01 to 0.5 WZcm 2 in power density.
- the processing time is preferably from 5 to 300 seconds, more preferably from 5 to 60 seconds. These conditions are much weaker than the previously reported RF sputtering treatment, but are sufficient for functional group formation on the surface. Conversely, if it is too strong or too long, it will undesirably damage the surface by excessively roughening the surface, generating a large amount of WBL, and changing the composition.
- the gas used in the RF bombardment treatment and the DC bombardment treatment is not particularly limited as long as it can generate plasma and generate a polar group on the surface after the surface treatment.
- a gas containing an inert gas such as He gas, Ne gas, Ar gas, Kr gas, or Xe gas is preferable.
- Treatment with a gas containing Ar gas is preferable because it is economical, easy to handle, and gives favorable results.
- oxygen-containing functional groups are added during bombardment treatment to remove WBL by treatment with a gas containing oxygen-containing compounds such as oxygen, carbon dioxide, carbon monoxide, ozone, water vapor, nitrous oxide, and acetone.
- the treatment with a gas containing a nitrogen-containing compound such as nitrogen, nitrogen dioxide, nitric oxide, or ammonia can generate a polar group and remove WBL.
- the surface treatment breaks the C--H bond, C--F bond, and C--C bond on the ETFE surface and improves the adhesion and adhesion by reacting with water and oxygen when exposed to the atmosphere, It generates polar groups such as carbonyl groups, and because it is under mild conditions under reduced pressure, it removes WBLs present on the surface without generating irregularities on the surface or generating new WBLs. Conceivable.
- a reactive gas such as oxygen
- the present inventors evaluated the evaluation of the adhesion and the adhesion of the surface-treated ETFE film.
- the fluorine transfer amount will be described.
- a fluororesin film such as an ETFE film is hot pressed with a substrate, the WBL present on the film surface is easily transferred to the substrate.
- the amount of transfer varies depending on the press temperature, surface pressure, and the type of substrate on the other side of the heat press.
- the WBL amount of the ETFE film In order to analyze the WBL amount of the ETFE film, it is appropriate to use a thin aluminum plate as the substrate and press it under the conditions of a surface pressure of S l kg fZcm 2 and a pressing temperature of 100.
- the amount of WBL can be evaluated by the total amount of fluorine atoms attached to the surface of the aluminum sheet.
- the ratio of the amount of fluorine atoms to the amount of aluminum atoms (fluorine atomic weight [atomic%] Z aluminum atomic weight [atomic%]) is defined as the amount of fluorine transfer based on the composition analysis value of the aluminum sheet surface by ESCA measurement. did.
- the amount of fluorine atoms present on the surface of the ETFE film surface-treated ETFE film, which is hot-pressed at 100 ° C. and a surface pressure of 21 kgf Zcm 2 for 10 minutes, cooled to room temperature, and then peeled off is given by
- the surface is preferably not more than one time the amount of fluorine atoms present on the surface of the untreated ETFE film on the surface of the untreated ETFE film, which was subjected to the hot pressing, cooled to room temperature, and peeled off.
- the amount of fluorine atoms present on the aluminum surface after exfoliation refers to all fluorine atoms present on the aluminum surface after exfoliation from the ETFE film and contained in all fluorine-containing molecules, polymers, compounds, etc. Is the sum of
- the surface roughness R of the surface of the treated film is also the untreated ETFE film. It is preferable that the surface roughness is not more than Ra .
- the present inventors heated and pressed an aluminum thin plate at a surface pressure of 21 kgf Zcm 2 at 100 ° C for 10 minutes with the treated surface of the surface-treated ETFE film facing upward, so that the surface in contact with the film was We further studied the relationship between the amount of fluorine atoms transferred onto an aluminum sheet and the adhesion and adhesion of the surface-treated ETFE film.
- Fluorine transfer is performed by pressing the aluminum sheet with the treated side of the surface-treated ETFE film facing up at a surface pressure of 21 kg iZcm 2 at 100 ° C for 10 minutes to transfer the aluminum sheet on the aluminum sheet in contact with the film.
- Figure 1 shows the correlation between the amount and the adhesion between the ETFE film and the EVA film.
- the amount of fluorine transfer is equal to or less than that of the untreated film. That is, the adhesion between the ETFE film and the EVA film is governed not by the amount of functional groups but by the amount of fluorine transfer. The smaller the amount of fluorine transfer, the greater the adhesion, the lower the amount of fluorine transfer.
- the untransferred film has a fluorine transfer amount of about 0.2. Therefore, the ETFE film of the present invention preferably has a fluorine transfer amount of 0.2 or less. In particular, a surface-treated ETFE film having a fluorine transfer amount of 0.1 or less has very good adhesion and adhesion.
- Fig. 2 shows the correlation between the amount of fluorine transfer and the adhesive strength of a laminate laminated with vinyl chloride using an adhesive (in this example, an adhesive containing a thermoplastic polyester resin component as a main component) 5 hours after boiling.
- an adhesive in this example, an adhesive containing a thermoplastic polyester resin component as a main component
- ETFE films with oxygen-containing functional groups on the film surface require sufficient adhesion to vinyl chloride (especially adhesion that can be maintained even under high temperature and high humidity conditions).
- the amount of fluorine transfer be small, and particularly the amount of fluorine transfer be equal to or less than that of the untreated film, that is, the amount of fluorine transfer be 0.2 or less.
- a surface-treated ETFE film with a fluorine transfer amount of 0.1 or less has very good adhesion and adhesion.
- Fig. 1 and Fig. 2 are examples of surface treatment with Ar gas.However, the relationship between the amount of fluorine transferred and the adhesive force and adhesive force is shown in other inert gas, oxygen gas, carbon dioxide gas, nitrogen gas. Similar results can be obtained by processing with a gas containing, for example. On the other hand, the amount of fluorine transfer of the film subjected to the conventional corona discharge treatment in air was as large as 0.98, and a surface-treated film having a lower amount of fluorine transfer than the untreated film could not be obtained.
- a surface-treated ETFE film wherein a hydroxyl group and a carbonyl group are present on the surface of the surface-treated film, and the surface roughness is 10 nm or less.
- An ETFE film is provided.
- the ETFE film of the present invention can be easily laminated to a so-called plastic sheet or film such as polyethylene, polypropylene, ABS, polystyrene, or polysalt using an adhesive.
- Epoxy adhesives, silicone adhesives, polyurethane adhesives, urea adhesives, melamine adhesives, phenolic resin adhesives, vinyl acetate adhesives, cyanoacrylate adhesives examples include synthetic resin adhesives represented by adhesives, etc. Also, emulsion adhesives represented by vinyl acetate resins dispersed in water, etc., and ethylene monovinyl acetate or polyamides. Hot-melt adhesives, synthetic rubber-based adhesives represented by chloroprene rubber, etc. Adhesive Ya silicone based adhesives.
- the above-mentioned adhesive it can be easily laminated with metals such as aluminum, SUS plate, galvanized steel plate, zinc-plated steel plate, and iron.
- the above adhesive can be used to laminate with a fluororesin such as ETFE and PFA (tetrafluoroethylene-perfluoro (alkoxyethylene) copolymer).
- a fluororesin such as ETFE and PFA (tetrafluoroethylene-perfluoro (alkoxyethylene) copolymer).
- polyester-based adhesives Particularly effective among the above adhesives are adhesives containing a thermoplastic polyester resin component (hereinafter referred to as polyester-based adhesives).
- the thermoplastic polyester resin is obtained by a dehydration condensation reaction between a dibasic acid and a diol.
- the dibasic acid include aliphatic dibasic acids such as adibic acid, azelaic acid, sebacic acid, succinic acid, and suberic acid, and aromatic dibasic acids such as isophthalic acid, terephthalic acid, orthophthalic acid, and naphthalene dicarboxylic acid.
- Basic acids are exemplified.
- the diols include ethylene glycol, diethylene glycol, 1,4-butanediol, 1,6-hexanediol, neopentyldaricol, and the like.
- thermoplastic polyester resin is preferably synthesized by a dehydration condensation reaction at about 240 ° C.
- additive can be used in combination with the thermoplastic polyester resin to improve the properties as an adhesive.
- Additives are, for example, flow modifiers such as benzoin, dimethyl terephthalate and the like.
- an isocyanate group-containing compound as a curing agent can be used in combination to improve the adhesive strength.
- the polyester resin in order to improve the adhesive strength with a fibrous substrate such as a woven fabric, can be modified with urethane to increase the adhesiveness.
- the polyester resin may be epoxy-modified so that the polyester-based adhesive is bonded to both the surface-treated fluororesin and the metal.
- Epoxy modification is carried out by synthesizing the polyester resin and then performing terminal epoxy modification (preferably by adding a predetermined amount of an epoxy resin such as bisphenol A type and reacting at about 180 ° C).
- Terminal epoxy modification preferably by adding a predetermined amount of an epoxy resin such as bisphenol A type and reacting at about 180 ° C.
- Will be Epoxy modification is effective not only for improving the adhesion to metals, but also extremely effective for improving the boiling water resistance and chemical resistance.
- Epoxy modification is performed by adding an appropriate amount of epoxy resin to modify the terminal carboxyl groups of the previously synthesized polyester resin into epoxies.
- the preferred amount of the epoxy resin to be added depends on the type of the substrate to be bonded to the ETFE film. For example, when bonding an ETFE film to a metal, an amount of epoxy resin necessary to completely modify the terminal carboxyl groups of the polyester resin is added, or the heat of the epoxy-modified polyester resin when the adhesive is heated. It is advisable to add an excess of epoxy resin so that free epoxy resin which does not participate in the modification is present so as not to hinder the flow. Meanwhile, ETFE film When is bonded to vinyl chloride, the modification with the epoxy resin may be slight or not. (That is, the amount of the epoxy resin added to the polyester resin is small or no.) This is because the epoxy resin swells due to the plasticizer contained in the vinyl chloride, and as a result, the cohesive strength tends to decrease.
- Epoxy resins used for epoxy modification include bisphenol A-type resin having the above-mentioned bisphenol skeleton, hydrogenated bisphenol A-type resin, diol-type resin whose bisphenol skeleton has been changed to a flexible methylene chain, and ether chain.
- Daricol type resin is exemplified.
- the glass transition point of the adhesive when cured can be arbitrarily changed.
- a bisphenol A type epoxy resin having an epoxy equivalent of about 50,000 to about 1000 is effective.
- an epoxy-modified polyester-based adhesive and a resin-modified polyester-based adhesive can be used in combination with a curing agent.
- a polyisocyanate containing two or more isocyanate groups per molecule is used.
- aromatic polyisocyanates such as tolylene diisocyanate, 4,4'-diphenylmethane diisocyanate, xylylene diisocyanate, and alicyclic polyisocyanates such as isophorone diisocyanate. Examples thereof include aliphatic polyisocyanates such as hexamethylene diisocyanate.
- adducts, burettes, and isocyanurates of the polyisocyanate and trimethylolpropane are also exemplified. Since the two-liquid type combined with a curing agent has a pot life, it is more preferable to use a so-called block isocyanate which dissociates at a high temperature and functions as a curing agent.
- thermoplastic polyester resins are not particularly limited to the examples described below.
- the applied thickness of the adhesive is preferably 3 / zm or more in terms of the applied thickness after drying.
- a thickness of 5 to 10 m is appropriate.
- the thickness is preferably about 20.
- the method of laminating is not particularly limited, but a so-called dry laminating method in which the solvent is evaporated after the application of the adhesive and then laminated is suitable.
- laminating it is further passed through a nip roll maintained at a temperature equal to or higher than the solvent drying temperature. Adhesion increases.
- additives such as a pigment, a leveling agent, an antifoaming agent, and an ultraviolet absorber can be added to these adhesives.
- the present invention provides a method for producing a laminate, comprising laminating an ETFE film whose surface has been subjected to an RF bombardment treatment or a DC bombardment treatment and another substrate by a dry lamination method.
- the present invention also provides an ETFE film whose surface has been subjected to RF bombardment treatment or DC bombardment treatment, applying an adhesive for lamination, then drying the adhesive, and then applying another substrate and the surface treatment.
- a method for producing a laminate characterized in that the obtained tetrafluoroethylene-ethylene copolymer film is adhered with the adhesive and laminated by a dry lamination method.
- Both sides of the ETFE film can be processed by RF bombardment or DC bombardment.
- the adhesive may be applied only to the surface to be bonded to another substrate.
- the adhesive is preferably an adhesive containing a thermoplastic polyester resin component as a main component for the same reason as described above.
- the bombardment treatment is preferably a bombardment treatment using a gas that causes a polar group to be present on the film surface after the bombardment treatment.
- the substrate for example, plastic sheets such as vinyl chloride resin (including those other than soft), polyester resin and polyethylene resin, and metal plates such as SUS plate, galvanized steel plate, galvanized steel plate, and aluminum plate are preferably used. It is.
- the pressure is preferably 5 to 10 kg fZcm.
- the laminate thus manufactured is preferably subjected to thermal curing, but sufficient adhesive strength can be obtained even at room temperature of about 25 ° C.
- the substrate to be laminated with the ETFE film by this laminating method is not limited to fluorine-free plastics represented by polyvinyl chloride, polyester, polypropylene, acrylic, etc., and various types of fluororesins can also be laminated. .
- a method of laminating an ETFE film and a metal a method of hot-melting the film at a melting point or higher on a metal plate having an increased bonding area by sandblasting or etching with a chemical, or using an adhesive is used.
- a method of performing thermal lamination at a temperature of about 70 to 230 ° C. is adopted.
- the ETFE laminated metal sheet by the former method is a lamination method that utilizes the excellent melt adhesion of ETFE to metal, and is excellent in adhesion and boiling water resistance.
- the equipment is large-scale, which is not preferable in terms of cost.
- the latter method by selecting an appropriate adhesive, firmly adheres at the time of lamination, but due to surface treatment to adhere, A new WBL layer was formed on the surface of the fluorine film, making it impossible to produce a laminate with excellent boiling water resistance.
- the ETFE film and the metal plate can be bonded to each other by a general dry lamination method as shown in FIG. 8, for example. According to this method, laminating at a processing speed of 5 to 4 OmZ is possible, and sufficient workability is obtained. Also, curing after lamination is not necessary.
- a nip roll When laminating, it is preferable to pass through a nip roll. If a nip roll is used in the above-described method for producing a laminate, an adhesive is applied to a metal plate, dried, and then the ETFE film and the metal plate are sandwiched between nipples. The two can be glued together alone, which is extremely excellent in mass productivity.
- the linear pressure is preferably 5 to 10 kgf / cm.
- the adhesive sufficiently follows the elongation of the ETFE film or the steel sheet even when the laminate is bent.
- Substrates to be laminated with the ETFE film by this lamination method include SUS plates, galvanized steel plates, galvanized steel plates, and aluminum.
- the laminate of the ETFE film and vinyl chloride is suitable for unit bath wall materials, coating booth wall materials, wallpaper, and the like.
- the laminate of ETFE film and stainless steel is Suitable for gas stove tops and range hoods.
- Laminate of ETFE film and aluminum is suitable for kitchen front panel
- FIG. 3 is a schematic cross-sectional view illustrating the RF bombard apparatus 10 used for the surface treatment of the ETFE film in Examples 1 to 15 and Comparative Examples 1 and 2.
- the electrode 4 and the counter electrode 5 are arranged in the decompression vessel 1 so as to face each other.
- the counter electrode 5 is grounded, and the electrode 4 is connected to the RF power supply 2 via the matching box 3.
- Atmospheric gas is supplied from the gas cylinder 8 through the atmospheric gas introducing valve 7 into the decompression container 1, and the inside of the decompression container 1 is exhausted through the exhaust port 6 by a vacuum pump (not shown), and Maintained at pressure.
- the ETFE film (trade name: Aflex, manufactured by Asahi Glass Co., Ltd., thickness of 50 mm) to be surface-treated was placed on either the counter electrode (anode) 5 or the electrode (force sword) 4. The distance between the electrode 4 and the counter electrode 5 was 4 cm.
- the atmospheric gas introduced into the decompression vessel 1 was any of Ar, CO 2 , O 2, and N 2 .
- the pressure in the depressurizing vessel 1 was set to 0.67 Pa, 6.7 Pa, or 67 Pa.
- a 13.56 MHz high frequency voltage was applied between electrode 4 and counter electrode 5.
- the RF power density was 0.16 WZcm 2 .
- the processing time was 5, 30, 100, or 300 seconds.
- surface-treated ETFE films were obtained.
- an ETFE film (Comparative Example 1) and a non-surface-treated ETFE film (Comparative Example 2) that had been subjected to corona treatment 200 W ⁇ minZm 2 in air, the same applies to the following corona treatment) were used.
- corona treatment 200 W ⁇ minZm 2 in air
- a dibasic acid composed of 50 mol% of terephthalic acid, 30 mol% of isophthalic acid, and 20 mol% of suberic acid was prepared as a dibasic acid.
- the diol a diol consisting of 30 mol% of ethylene glycol and 70 mol% of 1,4-butanediol was prepared.
- These dibasic acids and diols were mixed at a molar ratio of about 1: 1 and reacted at 240 ° C. for 10 hours to obtain a polyester resin having a number average molecular weight of 30,000.
- the acid value of this polyester resin was 3.
- terephthalic acid use 50 mol% of terephthalic acid, 30 mol% of isophthalic acid, 20 mol% of suberic acid as dibasic acid, 20 mol% of ethylene glycol as diol, and 80 mol% of neopen tildaricol at 240 ° C.
- a polyester resin having a number average molecular weight of 30,000 was obtained, and this resin was used as adhesive B.
- the ETFE film and transparent vinyl chloride were laminated at a linear pressure of 10 kgf / cm.
- the bonding conditions were 120 at 1 second when the adhesive A was used, and 70 at 1 second when the adhesive B was used.
- Examples 1 to 15 of the present invention all show excellent adhesiveness. In addition, it can be seen that all of Examples 1 to 15 maintain excellent adhesiveness even after boiling. On the other hand, in Comparative Example 1 subjected to corona treatment, the adhesive strength after boiling was particularly low, and in Comparative Example 2 not treated, both the adhesive strength under normal conditions and after boiling were low.
- each ETFE film (15 cm x 8 cm) obtained by performing the surface treatment in the same manner as in Examples 1 to 15, EVA (hindered amine light stabilizer 700 ppm, heat stabilizer 500 ppm, UV absorber 3000 ppm (Vinyl ethylene acetate copolymer with a content of added vinyl acetate of 6% by weight and a thickness of 470 m)
- EVA hindered amine light stabilizer 700 ppm, heat stabilizer 500 ppm, UV absorber 3000 ppm (Vinyl ethylene acetate copolymer with a content of added vinyl acetate of 6% by weight and a thickness of 470 m)
- the film was pressed for 15 minutes at a surface pressure of 10 kg iZcm 2 by a metal press set at 145 ° C in advance. And laminated. After lamination and cooling to room temperature, a T-peeling test was performed at a pulling speed of 5 OmmZ to measure the adhesion between the ET FE film
- FIG. 4 is a schematic cross-sectional view illustrating the DC bombard apparatus 20 used in the surface treatment of the ETFE film in Examples 31 to 45.
- the electrode 14 and the counter electrode 15 are arranged in the decompression vessel 11 so as to face each other.
- the opposite electrode 15 is grounded, and the electrode 14 is connected to the DC power supply 12.
- Atmospheric gas is supplied from the gas cylinder 18 into the decompression vessel 11 through the atmosphere gas introduction valve 17, and the inside of the decompression vessel 11 is exhausted by the vacuum pump (not shown) through the exhaust port 16. It is maintained at a predetermined pressure.
- the surface-treated ETFE film (trade name: Aflex, manufactured by Asahi Glass Co., Ltd., 50 m thick) was placed either on the counter electrode (anode) 15 or on the electrode (force sword) 14. The distance between the electrode 14 and the counter electrode 15 was 4 cm.
- the atmospheric gas introduced into the decompression vessel 11 was any of Ar, CO 2 , O 2 , and N 2 .
- the pressure in the decompression container 1 was set to 0.67 Pa, 6.7 Pa, or 67 Pa.
- a DC voltage was applied between the electrode 14 and the counter electrode 15.
- the DC power density was 0.1 leWZcm 2 .
- the processing time was 5, 30, 100, or 300 seconds. Under the conditions shown in Table 3, for Examples 31 to 45, surface-treated ETFE films were obtained.
- Table 3 shows the case where the adhesive A was used, but similar results were obtained when the adhesive B was used.
- Examples 31 to 45 of the present invention all show excellent adhesiveness. In addition, it can be seen that Examples 31 to 45 all maintain excellent adhesiveness even after boiling.
- the surface functional groups on the surface of the surface-treated ETFE film were examined.
- the surface functional groups were identified by the ESCA method and the chemical modification method.
- ls and 5 peaks on the surface of the surface-treated ETFE film were measured, and the functional group was identified from the chemical shift.
- the peak was fitted with a Gaussian bite-by-Lenz function to separate each component, and each functional group was identified from the chemical shift of each separated component.
- the correspondence between the chemical shift and the functional group was determined by calculating the orbital energy of the unit structure molecule by the molecular orbital method (ab-initio method).
- a sample containing a hetero atom that selectively reacts with a specific functional group is used.
- the presence or absence of a specific functional group was analyzed by reacting a chemical gas onto the surface of the surface-treated ETFE film and measuring the presence or absence of heteroatoms on the ETFE film surface using ESCA.
- the carbonyl group is identified by exposing the surface-treated ETFE film to the vapor of a hydrazine aqueous solution (1: 1) for 4 hours, and then analyzing the surface of the ETFE film with ESCA to check for N on the surface. Was. If there are carbonyl groups on the surface,
- N is present on the surface of the ETFE film.
- the surface treatment of the ETF E film was performed in the same manner as in Example 2, and Example 6 was performed.
- FIG. 5 shows the results of ESCA measurement of the surface of this ETFE film.
- Fig. 6 shows the results of ESC A measurement of the surface of the corona-treated film (Comparative Example 5).
- Each is a 1 S spectrum.
- Each of these peaks had a peak top in the binding energy range of 533 to 534 eV.
- these peaks were fitted with a Gaussian-Lorentz function to separate each component A and B, and each functional group was identified from the chemical shift of each separated component. Peak A was presumed to be a hydroxyl group, and peak B was presumed to be a carbonyl group.
- Examples 62, 63, 64, and 65 obtained by subjecting the ETFE film to surface treatment in the same manner as in Examples 2, 11, 13, and 15 and the corona-treated film (Comparative Example 6) ) was identified by a chemical modification method.
- An untreated ETFE film was also used to confirm the effect of physical adsorption (Comparative Example 7).
- Table 5 shows the results. In Table 5, those in which the reaction element contained the reaction element were detected were marked with " ⁇ ", and those in which the reaction element was not detected were marked with "one". [Table 5]
- the ETFE films of Examples 62, 63, 64 and 65 and the ETFE films of Comparative Examples 6 and 7 were exposed to the vapor of a hydrazine aqueous solution (1: 1) for 4 hours, and then the surface of the ETFE film was analyzed by ESCA. The presence or absence of N on the surface was examined. As a result, N was detected in the ETFE films of Examples 62, 63, 64 and 65 and the ETFE film of Comparative Example 6, and N was detected on the surfaces of the ETFE films of Examples 62, 63, 64 and 65 and the ETFE film of Comparative Example 6. Was found to have a carbonyl group. There was no detectable amount of carbonyl groups on the ETFE film surface of Comparative Example 7.
- the ETFE film of Comparative Example 7 was not modified at all by the chemical modification using any of the reagents. Therefore, none of the hydroxyl group and carboxyl group detected in the ETFE films of Examples 62, 63, 64, and 65 and the carboxyl group detected in the ETFE film of Comparative Example 6 were due to physical adsorption of the reagent.
- the instrument used for the ESCA measurement was a PHI 5500 type instrument.
- the X-ray source used was a monochromatic A1 ⁇ ray at 14 kV, 500 W, and the X-ray irradiation area was 7 mm X 2 mm.
- (Photoelectron detection area) was 0.8 mm ⁇ , the photoelectron detection angle was 70 °, the neutralizing electron beam energy was 0.1 leV, and the photoelectron Pass Energy was 23.5 eV.
- the surface treatment of the ETFE film was performed in the same manner as in Examples 1, 2, 10, 12, and 14, respectively, to obtain the ETFE films of Examples 66, 67, 68, 69, and 70, respectively.
- ETF E films of a corona-treated ETFE film (Comparative Example 8) and a non-surface-treated ETFE film (Comparative Example 9) were prepared.
- Table 6 shows the results of measurements of A in the non-contact operation dynamic mode using the AFM.
- the ETFE films of Examples 66 to 70 of the present invention were smaller than untreated ETF E films (Comparative Example 9).
- the surface treatment according to the invention does not reveal the surface of the film. This means that the surface treatment method in the present invention is a very uniform and gentle treatment.
- the ETFE films of Examples 66 to 70 of the present invention exhibited excellent adhesive strength and adhesive strength.
- the surfaces of the ETFE films of Examples 66 to 70 were not in a conspicuous uneven state (cone-shaped projections were not formed), and the crystal structure in the untreated state was not impaired. .
- the adhesion was measured in the same manner as in Example 1, and the adhesion was measured in the same manner as in Example 16.
- FIG. 7 is a schematic perspective view for explaining an apparatus and method for producing a laminate of an ETF film and a vinyl chloride film.
- the adhesive in the adhesive tank 32 is applied to the ETFE film 35 supplied from the ETF film roll 31 by the gravure roll 33. Thereafter, the adhesive is dried by a drying oven 34, and the ETFE film 35 provided with the dried adhesive and the polyvinyl chloride film 38 supplied from the vinyl chloride roll 37 are laminated by passing through the nipple 36. Then, a laminate 39 is manufactured.
- the adhesive used in this example is the same as the adhesive A used in Example 1.
- one side of a 50 m-thick ETFE film (trade name: Aflex, manufactured by Asahi Glass) was RF bombarded.
- the processing conditions were the same as in Example 2 described above.
- the ETFE film 35 having the adhesive layer after drying and a 200 m thick Shiridani vinyl film 38 were laminated by passing through a nip roll 36 maintained at 130 ° C. to obtain a laminate of Example 61.
- the linear pressure of the nip roll 36 was 10 kgfZcm, and the laminating speed was 12 mZmin.
- a T-pilling test was conducted at a pulling rate of 2 OmmZ minutes, and showed an adhesive strength of 1530 gf Zcm.
- the test piece was immersed in boiling water for 5 hours, and then subjected to a T-peeling test at a pulling speed of 20 mm / min. The result was 1490 gf Zcm, and no decrease in adhesive strength was observed.
- FIG. 8 is a schematic perspective view for explaining an apparatus and a method for manufacturing a laminate of an ETFFE film and a SUS plate.
- this manufacturing apparatus first, the adhesive in the adhesive tank 42 is applied to the SUS plate 45 supplied from the SUS plate roll 41 by the gravure roll 43. Thereafter, the adhesive is dried by a drying furnace 44, and the SUS plate 45 provided with the dried adhesive and the ETFE film 48 supplied from the ETFE film roll 47 are laminated by passing through a nipple 46. To produce a laminate 49, and finally, the laminate 49 is wound to form a laminate roll 50.
- Example 2 First, one side of a 50 m-thick ETFE film (trade name: Aflexs, manufactured by Asahi Glass) was subjected to RF bombardment treatment. The processing conditions were the same as in Example 2 described above. Next, the adhesive A prepared in Example 1 was applied to a SUS 430 plate 45 degreased with acetone using a gravure roll 43, and dried at 200 ° C. in a drying furnace 44. After drying, the adhesive layer 5 was dried. Obtained.
- a 50 m-thick ETFE film trade name: Aflexs, manufactured by Asahi Glass
- the ETFE film 48 subjected to the RF bombardment treatment as described above and the SUS430 plate 45 coated with the adhesive were laminated by passing through a nipple 46 maintained at 120 ° C.
- a laminate 49 was manufactured.
- the linear pressure of Nipple 46 was 10 kgf Zcm, and the laminating speed was 12 mZmin.
- a 180-degree pulling test was performed at a pulling rate of 2 OmmZ minutes, and an adhesive strength of 1500 gf Zcm was shown. When this test piece was immersed in boiling water for 5 hours, it showed an adhesive strength of 1440 gf Zcm. Was.
- the surface treatment of the ETFE film by DC bombardment treatment was performed in the same manner as in Examples 32 and 33, and the ETFE films of Examples 73 and 74 were obtained, respectively.
- the functional groups on the surface of these films were identified using a peak shift of £ 5 A and a chemical modification method in the same manner as in Examples 61 and 62, and it was found that hydroxyl groups and carbonyl groups were mainly present. all right.
- Example 73 the ETFE films of Examples 73 and 74 were used in the same manner as in Example 1 and the adhesive A was used to measure the adhesive strength between the ETFE films and a 200-m-thick transparent vinyl chloride, respectively.
- the adhesive A was used to measure the adhesive strength between the ETFE films and a 200-m-thick transparent vinyl chloride, respectively.
- a value of 1520 gfcm was obtained
- the ETFE film of Example 74 a value of 1490 ginocm was obtained, all showing high adhesive strength.
- the adhesive strength with a 200 m-thick transparent vinyl chloride was measured in the same manner as in Example 1.
- a value of 1,500 gf Zcm was obtained, and for the ETFE film of Example 74, a value of 1,470 gf Zcm was obtained, all showing high adhesive strength.
- Example 71 One side of a 50 m-thick ETFE film (trade name: Aflex, manufactured by Asahi Glass) was DC bombarded.
- the processing conditions were the same as in Example 33 described above.
- Example 71 In the same manner as in Example 1, lamination with a vinyl chloride film was performed, and a T-shaped pilling test was performed. As a result, an adhesive strength of 1470 gf Zcm was shown.
- the T-peeling test after immersing the test piece in boiling water for 5 hours showed an adhesive strength of 1460 g ⁇ / cm, and no decrease in the adhesive strength was observed.
- Example 10 One side of a 50 m-thick ETFE film (trade name: Aflex, manufactured by Asahi Glass) was DC-bonded. The processing conditions were the same as in Example 33 described above. In the same manner as in Example 72, an ETFE film was laminated on a SUS plate to produce a laminate. After standing at room temperature for one day, a 180-degree peeling test was conducted at a pulling speed of 20 mm / min. As a result, an adhesive strength of 1450 gf Zcm was shown. When the test piece was immersed in boiling water for 5 hours, it showed an adhesive force of 1480 gf / cm. (Comparative Example 10)
- one side of a 50 m-thick ETFE film (trade name: Aflex, manufactured by Asahi Glass) was subjected to corona discharge treatment in air.
- the above adhesive A was applied to the surface by gravure roll, dried at 100 ° C., and dried to obtain an adhesive layer of 5 / zm.
- the corona discharge treated ETFE film and a 200-inch thick vinyl chloride film were combined.
- Lamination was performed by passing through a nip roll maintained at 110 ° C.
- the linear pressure of the nip roll was 10 kgf Zcm, and the laminating speed was 12 mZ.
- a T-peeling test was performed at a pulling rate of 2 OmmZ minutes, and showed an adhesive strength of 1 170 gf / cm, but when immersed in boiling water for 5 hours, 720 gf It showed a low adhesive strength of Zcm.
- Example 77, 78, 79, and 80 the surface treatment was performed in the same manner as in Examples 1, 2, 4, and 5, and the adhesive strength was measured.
- Examples 81, 82, 83, and 84 the surface treatment was performed in the same manner as in Examples 32, 33, 35, and 36, and the adhesive strength was measured.
- Examples 85, 86, 87, 88, 89, and 90 the surface treatment was performed in the same manner as in Examples 10, 11, 12, 13, 14, and 15, and the adhesive strength was measured.
- Comparative Example 11 performed the same surface treatment as Comparative Example 1, and Comparative Example 12 had no surface treatment.
- Comparative Examples 11 and 12 the adhesive strength was measured in the same manner as in Comparative Examples 1 and 2, respectively.
- the aluminum sheet On the surface of the ETFE film of each of the above Examples and Comparative Examples, the aluminum sheet, the heating temperature 100 ° C, a surface pressure 21 8:] 11 2, press hot-pressing time 10 minutes, after cooling E TFE film to room temperature
- the amount of fluorine transfer on the aluminum surface (the surface that was in contact with the ETFE film) from which the film was peeled was measured.
- Table 7 shows the values of the adhesive strength and the amount of fluorine transfer.
- the amount of fluorine transfer of the ETFE film of the present invention is very small, which is lower than that of the film not subjected to surface treatment (Comparative Example 12). That is, the ETFE film subjected to the RF bombardment treatment or the DC bombardment treatment in the present invention has a small amount of fluorine transferred to the aluminum surface and exhibits excellent adhesive strength. In contrast, it can be seen that the fluorine transfer amount of the ETF E film subjected to the corona discharge treatment (Comparative Example 11) was large, that is, the fluorine amount transferred to the aluminum surface was large, and the adhesive strength was poor. As shown here, the adhesive force of the surface-treated ETF E film shows a high value when the amount of fluorine transfer is small.
- an ETFE film exhibiting extremely good adhesive strength, A laminate using the TFE film can be obtained.
- a laminate of an ETFE film having excellent adhesiveness and a plastic sheet such as vinyl chloride can be produced with good mass productivity.
- a laminate of an ETFE film having excellent adhesiveness and a metal plate such as SUS can be manufactured with high mass productivity.
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Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98911059A EP0970987B1 (en) | 1997-03-28 | 1998-03-27 | Fluororesin films, laminate produced by using the same, and process for producing laminate |
US09/381,633 US6534182B1 (en) | 1997-03-28 | 1998-03-27 | Fluororesin films, laminate produced by using the same, and process for producing laminate |
DE69819140T DE69819140T2 (de) | 1997-03-28 | 1998-03-27 | Fluorharzfilme, Laminat, das unter Verwendung desselben hergestellt ist, und Verfahren zur Herstellung eines Laminats |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP9/95006 | 1997-03-28 | ||
JP9500697 | 1997-03-28 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US09/381,633 A-371-Of-International US6534182B1 (en) | 1997-03-28 | 1998-03-27 | Fluororesin films, laminate produced by using the same, and process for producing laminate |
US10/310,865 Division US20030162029A1 (en) | 1997-03-28 | 2002-12-06 | Fluorine-type film, laminate employing it and process for producing the laminate |
Publications (1)
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WO1998044026A1 true WO1998044026A1 (fr) | 1998-10-08 |
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PCT/JP1998/001397 WO1998044026A1 (fr) | 1997-03-28 | 1998-03-27 | Films de resine fluoree, stratifies obtenus a partir dudit materiau, et procede de production desdits stratifies |
Country Status (4)
Country | Link |
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US (2) | US6534182B1 (ja) |
EP (1) | EP0970987B1 (ja) |
DE (1) | DE69819140T2 (ja) |
WO (1) | WO1998044026A1 (ja) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2008049706A (ja) * | 2007-08-23 | 2008-03-06 | Toyo Ink Mfg Co Ltd | 水性ウレタン樹脂及び水性印刷インキ組成物並びに該組成物を用いた包装材料 |
JP2009263529A (ja) * | 2008-04-25 | 2009-11-12 | Nippon Valqua Ind Ltd | フッ素樹脂系成形物の表面改質方法 |
JP2015189934A (ja) * | 2014-03-28 | 2015-11-02 | 大日本印刷株式会社 | プラズマ処理された表面平滑化フッ素系樹脂フィルムおよびその製造方法 |
WO2016021518A1 (ja) * | 2014-08-05 | 2016-02-11 | 株式会社 潤工社 | フッ素樹脂チューブ |
JP2020523440A (ja) * | 2017-06-09 | 2020-08-06 | ダウ グローバル テクノロジーズ エルエルシー | 溶媒系接着剤組成物 |
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US20030060299A1 (en) * | 1994-07-21 | 2003-03-27 | Brent Perrier | Glow-in-the-dark bowling game and method |
JP3791458B2 (ja) * | 2002-05-23 | 2006-06-28 | 旭硝子株式会社 | 離型フィルム |
KR20070102482A (ko) * | 2004-11-02 | 2007-10-18 | 아사히 가라스 가부시키가이샤 | 플루오로카본막 및 그 제조 방법 |
KR20070091132A (ko) * | 2004-12-03 | 2007-09-07 | 아사히 가라스 가부시키가이샤 | 에틸렌-테트라플루오로에틸렌계 공중합체 성형물 및 그제조 방법 |
KR100612411B1 (ko) | 2006-03-23 | 2006-08-16 | 류재학 | 태양전지모듈용 백시트 제조 공정 |
JP2008004500A (ja) * | 2006-06-26 | 2008-01-10 | Toyota Motor Corp | 燃料電池電解質膜用の多孔質膜とその製造方法 |
US20210146662A1 (en) * | 2017-05-31 | 2021-05-20 | Osaka University | Layered product and method for producing same |
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- 1998-03-27 EP EP98911059A patent/EP0970987B1/en not_active Expired - Lifetime
- 1998-03-27 US US09/381,633 patent/US6534182B1/en not_active Expired - Fee Related
- 1998-03-27 DE DE69819140T patent/DE69819140T2/de not_active Expired - Fee Related
- 1998-03-27 WO PCT/JP1998/001397 patent/WO1998044026A1/ja active IP Right Grant
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2002
- 2002-12-06 US US10/310,865 patent/US20030162029A1/en not_active Abandoned
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JPS51125455A (en) * | 1975-04-14 | 1976-11-01 | Jiyunkichi Nakai | Method of surface treatment of molded article |
JPS5577566A (en) * | 1978-12-08 | 1980-06-11 | Asahi Glass Co Ltd | Laminated vinyl chloride resin piece |
JPS60181135A (ja) * | 1984-02-29 | 1985-09-14 | Toray Ind Inc | 熱可塑性樹脂成形物 |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008049706A (ja) * | 2007-08-23 | 2008-03-06 | Toyo Ink Mfg Co Ltd | 水性ウレタン樹脂及び水性印刷インキ組成物並びに該組成物を用いた包装材料 |
JP4506797B2 (ja) * | 2007-08-23 | 2010-07-21 | 東洋インキ製造株式会社 | 水性ウレタン樹脂及び水性印刷インキ組成物並びに該組成物を用いた包装材料 |
JP2009263529A (ja) * | 2008-04-25 | 2009-11-12 | Nippon Valqua Ind Ltd | フッ素樹脂系成形物の表面改質方法 |
JP2015189934A (ja) * | 2014-03-28 | 2015-11-02 | 大日本印刷株式会社 | プラズマ処理された表面平滑化フッ素系樹脂フィルムおよびその製造方法 |
WO2016021518A1 (ja) * | 2014-08-05 | 2016-02-11 | 株式会社 潤工社 | フッ素樹脂チューブ |
JP2016037597A (ja) * | 2014-08-05 | 2016-03-22 | 株式会社潤工社 | フッ素樹脂チューブ |
US10155362B2 (en) | 2014-08-05 | 2018-12-18 | Junkosha Inc. | Fluororesin tube |
JP2020523440A (ja) * | 2017-06-09 | 2020-08-06 | ダウ グローバル テクノロジーズ エルエルシー | 溶媒系接着剤組成物 |
Also Published As
Publication number | Publication date |
---|---|
EP0970987A4 (en) | 2000-05-31 |
US20030162029A1 (en) | 2003-08-28 |
US6534182B1 (en) | 2003-03-18 |
DE69819140D1 (de) | 2003-11-27 |
DE69819140T2 (de) | 2004-08-26 |
EP0970987B1 (en) | 2003-10-22 |
EP0970987A1 (en) | 2000-01-12 |
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