WO2018230722A1 - 多層フィルム、積層体、エアバッグ、及び積層体の製造方法 - Google Patents
多層フィルム、積層体、エアバッグ、及び積層体の製造方法 Download PDFInfo
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- WO2018230722A1 WO2018230722A1 PCT/JP2018/022994 JP2018022994W WO2018230722A1 WO 2018230722 A1 WO2018230722 A1 WO 2018230722A1 JP 2018022994 W JP2018022994 W JP 2018022994W WO 2018230722 A1 WO2018230722 A1 WO 2018230722A1
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- Prior art keywords
- multilayer film
- base fabric
- adhesive layer
- layer
- laminate
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Definitions
- the present invention relates to a multilayer film, a laminate, an airbag, and a method for producing the laminate.
- Patent Document 1 discloses a laminate formed by laminating a thermoplastic elastomer on a fabric made of thermoplastic resin fibers.
- Patent Document 1 describes that the disclosed structure can improve the mechanical strength of the laminate and prevent the occurrence of pinholes.
- adhesion under high temperature and / or high humidity conditions is described. Sex has not been studied. Also, the cost is not taken into consideration.
- an object of one embodiment of the present invention is to provide a multilayer film that is excellent in adhesiveness under high temperature and / or high humidity conditions and can be manufactured at low cost.
- an embodiment of the present invention is a multilayer film that is used by being bonded to a base fabric, and is bonded to the adhesive layer to be bonded to the base fabric and the adhesive layer.
- the adhesive layer contains a thermoplastic polyester elastomer and a resin having a Shore D hardness of less than 80.
- the present invention it is possible to provide a multilayer film that has excellent adhesion under high temperature and / or high humidity conditions and can be manufactured at low cost.
- FIG. 1 shows a schematic cross-sectional view of the multilayer film 1.
- One embodiment of the present invention is a multilayer film 1 having an airtight layer 2 and an adhesive layer 3 bonded to the airtight layer 2 as shown in FIG.
- the multilayer film 1 is used by being bonded to a base fabric, and the adhesive layer 3 is a side bonded to the base fabric.
- an airtight layer is a layer having a function of preventing gas from flowing inside and outside the layer.
- the adhesive layer is a layer having adhesiveness to the base fabric, and the adhesiveness is expressed by softening or melting under a predetermined condition, for example, a temperature and / or pressure increased condition. May be.
- a predetermined condition for example, a temperature and / or pressure increased condition.
- the multilayer film according to this embodiment has a structure of at least two layers having an airtight layer and an adhesive layer. Thereby, each layer can have an adhesion function when the film is adhered to the base fabric and an airtight function in the obtained laminate. Therefore, when the multilayer film according to the present embodiment is used, the adhesion to the base fabric (the delamination resistance between the base fabric and the thermoplastic film) and the case where the single layer film is adhered to the base fabric, and A high-quality laminate having both airtightness can be produced.
- the adhesive layer contains a thermoplastic polyester elastomer and a resin having a Shore D hardness of less than 80, it has excellent adhesiveness after being stored at high temperature and / or high humidity. Further, since the amount of the relatively expensive thermoplastic polyester elastomer can be reduced, a multilayer film can be produced at low cost.
- Shore D hardness is the hardness measured using a type D durometer in the method prescribed
- the multilayer film according to the present embodiment can be favorably bonded to the base fabric using heat without using an adhesive or the like, labor and cost due to the use of the adhesive can be reduced. Moreover, when using it for a long period of time, or when using it in a high-temperature, high-humidity environment, it can prevent that a laminated body loses a softness
- the adhesive layer includes a thermoplastic polyester elastomer and a polymer having a Shore D hardness of less than 80.
- the delamination resistance of the obtained laminate can be improved at a low cost. That is, the adhesiveness between the adhesive layer and the base fabric and the adhesiveness between the adhesive layer and the airtight layer can be improved at normal temperature and at high temperature and / or high humidity. Moreover, the softness
- the adhesive layer includes a thermoplastic elastomer and a thermoplastic resin, and more specifically, may include a thermoplastic polyester elastomer and an ethylene-vinyl acetate copolymer.
- the delamination resistance of the obtained laminate can be improved at a low cost. That is, the adhesiveness between the adhesive layer and the base fabric and the adhesiveness between the adhesive layer and the airtight layer can be improved at normal temperature and at high temperature and / or high humidity. Moreover, the softness
- the thermoplastic elastomer is preferably a block copolymer including a hard segment (also referred to as a high melting point segment or a crystalline segment) and a soft segment (also referred to as a low melting point segment or an amorphous segment).
- a thermoplastic elastomer can be softened by heat to exhibit fluidity, and can exhibit rubber-like elasticity in a state where no heat is applied.
- the adhesiveness to the base fabric can be improved by including a thermoplastic polyester elastomer in the adhesive layer. Moreover, the flexibility and mechanical strength of the obtained laminate can be improved, and deterioration under a high temperature environment and / or a high humidity environment can be prevented.
- the thermoplastic polyester elastomer may be a polyester / polyether type mainly containing an aromatic polyester or the like as a hard segment and mainly containing an aliphatic polyether or the like as a soft segment, or mainly an aromatic polyester or the like as a hard segment. It may be a polyester / polyester type containing an aliphatic polyester as a soft segment.
- the hard segment of the thermoplastic polyester elastomer is preferably a segment containing an aromatic polyester, for example, a polyester formed of an aromatic dicarboxylic acid component and a diol component.
- aromatic dicarboxylic acid used as the aromatic dicarboxylic acid component examples include terephthalic acid, isophthalic acid, phthalic acid, naphthalene-2,6-dicarboxylic acid, naphthalene-2,7-dicarboxylic acid, anthracene dicarboxylic acid, diphenyl-4,4 Examples include '-dicarboxylic acid, diphenoxyethanedicarboxylic acid, 4,4'-diphenyl ether dicarboxylic acid, 5-sulfoisophthalic acid, and sodium 3-sulfoisophthalate.
- the aromatic dicarboxylic acid component may be contained alone or in combination of two or more in the aromatic polyester. In the hard segment, a part of the aromatic dicarboxylic acid component may be replaced with an alicyclic or aliphatic carboxylic acid.
- diol as the diol component examples include diols having a molecular weight of 400 or less, for example, aliphatic diols such as 1,4-butanediol, ethylene glycol, trimethylene glycol, pentamethylene glycol, hexamethylene glycol, neopentyl glycol, and decamethylene glycol.
- diols having a molecular weight of 400 or less for example, aliphatic diols such as 1,4-butanediol, ethylene glycol, trimethylene glycol, pentamethylene glycol, hexamethylene glycol, neopentyl glycol, and decamethylene glycol.
- the diol component may be contained alone or in combination of two or more in the aromatic polyester.
- the polyester contained in the hard segment is preferably polybutylene terephthalate, polyethylene terephthalate, or polytrimethylene terephthalate, and more preferably polybutylene terephthalate, from the viewpoints of heat resistance and gas barrier properties.
- the soft segment of the thermoplastic polyester elastomer preferably contains an aliphatic polyether and / or an aliphatic polyester.
- Aliphatic polyethers include poly (ethylene oxide) glycol, poly (propylene oxide) glycol, poly (tetramethylene oxide) glycol (polytetramethylene ether glycol), poly (hexamethylene oxide) glycol, and the copolymer weight of ethylene oxide and propylene oxide.
- the aliphatic polyester include poly ( ⁇ -caprolactone), polyenantlactone, polycaprylolactone, polybutylene adipate, and polyethylene adipate.
- poly (tetramethylene oxide) glycol poly (propylene oxide) glycol ethylene oxide addition polymer, ethylene oxide and tetrahydrofuran copolymer Glycol, poly ( ⁇ -caprolactone), polybutylene adipate, polyethylene adipate and the like are preferable, and among these, poly (tetramethylene oxide) glycol (polytetramethylene ether glycol), poly (propylene oxide) glycol ethylene oxide addition polymer And a copolymer glycol of ethylene oxide and tetrahydrofuran is preferred.
- the number average molecular weight of the soft segment is preferably about 300 to 6000 in the copolymerized state.
- thermoplastic polyester elastomer may be modified with an unsaturated carboxylic acid such as acrylic acid, maleic acid or fumaric acid or a derivative thereof in the presence of a radical generator.
- unsaturated carboxylic acid or derivative thereof added for modification is preferably 0.1 to 30 parts by weight with respect to 100 parts by weight of the thermoplastic polyester elastomer.
- the kind and amount of the components used for such modification can be appropriately selected according to the material and application of the base fabric to be bonded.
- the content ratio of the hard segment in the thermoplastic polyester elastomer in the adhesive layer is preferably 10 to 60% by weight and more preferably 20 to 40% by weight with respect to 100% by weight of the thermoplastic polyester elastomer.
- the content ratio of the hard segment in the thermoplastic polyester elastomer in the adhesive layer is preferably 10 to 60% by weight and more preferably 20 to 40% by weight with respect to 100% by weight of the thermoplastic polyester elastomer.
- the content ratio of the soft segment in the thermoplastic polyester elastomer in the adhesive layer is preferably 50 to 90% by weight and more preferably 60 to 80% by weight with respect to 100% by weight of the thermoplastic polyester elastomer.
- the content ratio of the soft segment in the thermoplastic polyester elastomer in the adhesive layer is preferably 50 to 90% by weight and more preferably 60 to 80% by weight with respect to 100% by weight of the thermoplastic polyester elastomer.
- the content of the soft segment in the thermoplastic polyester elastomer is related to the melting point and softening point of the thermoplastic polyester elastomer. Generally, the higher the soft segment content in the thermoplastic polyester elastomer, the lower the melting point and softening point of the thermoplastic polyester elastomer. Therefore, the melting point of the thermoplastic polyester elastomer can be adjusted by adjusting the content ratio of the soft segment in the thermoplastic polyester elastomer in the adhesive layer, and consequently the melting point of the adhesive layer can be adjusted.
- the melting point of the thermoplastic polyester elastomer used for the adhesive layer is preferably 80 ° C. or higher, more preferably 100 ° C. or higher, and further preferably 130 ° C. or higher.
- the upper limit of the melting point of the thermoplastic polymer used for the adhesive layer is not particularly limited as long as it is lower than the melting point of the hermetic layer, but is preferably 250 ° C. or lower, more preferably 200 ° C. or lower, 170 More preferably, it is below °C.
- fusing point can be made into the melting peak temperature measured with the differential scanning calorimeter.
- the adhesive layer can contain two or more of the above-mentioned thermoplastic polyester elastomers. Further, in addition to the thermoplastic polyester elastomer, it contains at least one other thermoplastic elastomer that is not polyester, for example, polyamide elastomer, polyolefin elastomer, polyurethane elastomer, polystyrene elastomer, polybutadiene elastomer, etc. Can do.
- thermoplastic polyester elastomers include “Hytrel (registered trademark)” manufactured by Toray DuPont Co., Ltd., “Primary (registered trademark)” manufactured by Mitsubishi Chemical Corporation, and “Perprene (registered trademark)” manufactured by Toyobo Co., Ltd. ) ”Series and the like.
- thermoplastic polyester elastomer In addition to the thermoplastic polyester elastomer described above, a polymer having a Shore D hardness of less than 80 can be used for the adhesive layer. As a result, the manufacturing cost of the multilayer film can be reduced and the flexibility can be improved while maintaining the advantages of the thermoplastic polyester elastomer, that is, the mechanical strength, heat resistance, durability under high temperature and high humidity, etc. .
- the type of polymer having a Shore D hardness of less than 80 is not particularly limited, but is less expensive than thermoplastic polyester elastomers, and can improve the flexibility of the adhesive layer when mixed with thermoplastic polyester elastomers. Preferably there is. More specifically, the polymer having a Shore D hardness of less than 80 is more preferably a polymer or copolymer (also referred to as a polyethylene polymer) containing an olefin unit such as an ethylene unit or a propylene unit as a monomer unit.
- thermoplastic elastomer When the polymer having a Shore D hardness of less than 80 is a thermoplastic elastomer, a hydrogenated thermoplastic elastomer (hydrogenated thermoplastic elastomer) is preferable, and a thermoplastic hydrogenated styrene-based elastomer is more preferable.
- polymers having a Shore D hardness of less than 80 include ethylene-vinyl acetate copolymer, polyethylene, hydrogenated styrene thermoplastic elastomer, and ethylene-butyl acrylate copolymer.
- polyethylene is preferably low density polyethylene. These polymers can be used singly or in combination of two or more.
- the vinyl acetate component of the ethylene-vinyl acetate copolymer is preferably 5 to 50% by weight based on the total ethylene-vinyl acetate copolymer.
- the content of the polymer having a Shore D hardness of less than 80 in the adhesive layer is preferably 1 to 60% by weight, and more preferably 10 to 50% by weight.
- the content ratio of the polymer having a Shore D hardness of less than 80 1% by weight or more the manufacturing cost can be suppressed and the flexibility can be improved.
- the content ratio 60% by weight or less the mechanical strength of the multilayer film can be increased. Can be improved.
- additives such as pigments, fillers, antioxidants, hydrolysis stabilizers, and antiblocking agents.
- the total thickness of the adhesive layer is preferably 5 to 50 ⁇ m, and more preferably 5 to 30 ⁇ m.
- thermoplastic elastomer examples include polyamide elastomers, polyolefin elastomers, polyurethane elastomers, polystyrene elastomers, polybutadiene elastomers, and the like.
- thermoplastic polyester elastomer for the airtight layer because it is the same elastomer as the thermoplastic elastomer contained in the adhesive layer. Since both the airtight layer and the adhesive layer contain a polyester-based elastomer, the adhesiveness between the adhesive layer and the airtight layer (delamination resistance) can be maintained under normal temperature and / or high humidity conditions. It can also be improved below.
- thermoplastic polyester elastomer When a thermoplastic polyester elastomer is used for the airtight layer, it can be selected from those described for the thermoplastic polyester elastomer in the adhesive layer.
- the type of hard segment in the thermoplastic polyester elastomer used in the hermetic layer is the same as the type of hard segment in the thermoplastic polyester elastomer used in the adhesive layer. It may be different or different. Further, the kind of soft segment in the thermoplastic polyester elastomer used in the airtight layer and the kind of soft segment in the thermoplastic polyester elastomer used in the adhesive layer may be the same or different from each other. Also good.
- the types of hard segments and soft segments in the thermoplastic polyester elastomer used in the airtight layer, and the types of hard segments and soft segments in the thermoplastic polyester elastomer used in the adhesive layer may be the same as or different from each other.
- the types of segments are the same, the bonding strength between the airtight layer and the adhesive layer is increased, and delamination does not easily occur in the multilayer film, and the mechanical strength of the multilayer film and the laminate is further increased. Can be improved.
- the melting point of the thermoplastic polyester elastomer used for the hermetic layer is preferably higher than the melting point of the adhesive layer.
- the melting point of a layer is a temperature at which the layer softens when the temperature of the layer is raised, the molecules of the polymer in the layer start relative movement, and the polymer becomes fluid. Point to. Therefore, it can be said that the melting points of the adhesive layer and the hermetic layer are the melting points of the polymers (including the polymer alloy) in the adhesive layer and the hermetic layer, respectively.
- the melting point of such a polymer can be the melting peak temperature measured with a differential scanning calorimeter.
- the difference between the melting point of the hermetic layer and the melting point of the adhesive layer can be preferably 10 to 100 ° C. or less, more preferably 20 to 80 ° C. or less. More preferably, it is over 20 ° C.
- the temperature can be easily controlled by setting the difference between the melting point of the hermetic layer and the melting point of the adhesive layer within the above range. Thereby, it is possible to reduce the occurrence of defective products in which the adhesive layer is not sufficiently softened and cannot perform the adhesive function, or the airtight layer is softened and deformed or altered, etc. Production stability can be improved.
- the melting point of the hermetic layer is preferably 100 ° C, more preferably 150 ° C or higher, and further preferably 180 ° C or higher.
- the upper limit of the melting point of the thermoplastic polymer used for the hermetic layer is not particularly limited, but is preferably 300 ° C. or less, more preferably 270 ° C. or less in consideration of ease of handling at the time of forming the multilayer film. More preferably, it is 230 ° C. or lower.
- the hard segment content in the thermoplastic polyester elastomer is preferably 40 to 95% by weight with respect to 100% by weight of the thermoplastic polyester elastomer. More preferably, it is 90% by weight.
- the mechanical strength of a multilayer film and a laminated body, heat resistance, and durability under high temperature and high humidity can be improved.
- moderate elasticity, flexibility, and a moldability of a multilayer film and a laminated body can be ensured by setting it as 95 weight% or less.
- the content ratio of the soft segment in the thermoplastic polyester elastomer is preferably 5 to 60% by weight and more preferably 10 to less than 50% by weight with respect to 100% by weight of the thermoplastic polyester elastomer.
- the content ratio of the soft segment in the thermoplastic polyester elastomer is preferably 5 to 60% by weight and more preferably 10 to less than 50% by weight with respect to 100% by weight of the thermoplastic polyester elastomer.
- the value (Psa / Pss) of the ratio of the soft segment content ratio (Psa) in the thermoplastic polyester elastomer in the adhesive layer to the soft segment content ratio (Pss) in the thermoplastic polyester elastomer in the airtight layer is 1.2 to 5 is preferable, and 1.4 to 3.5 is more preferable.
- the hermetic layer contains a thermoplastic polyester elastomer
- it can contain two or more of the above-mentioned thermoplastic polyester elastomers.
- another thermoplastic elastomer which is not polyester type can be mix
- additives such as pigments, fillers, antioxidants, hydrolysis stabilizers, and antiblocking agents.
- the total thickness of the hermetic layer is preferably 5 to 50 ⁇ m, and more preferably 5 to 30 ⁇ m.
- the multilayer film has an airtight layer and an adhesive layer.
- the adhesive layer may be a single layer or a plurality of adhesive layers.
- the materials constituting each adhesive layer may be the same or different.
- the melting points of the layers of the plurality of adhesive layers may be the same or different.
- the airtight layer may be a single layer or a plurality of layers.
- the material and melting point of each hermetic layer may be the same or different.
- a pigment such as a pigment can be added to either the first adhesive layer or the second adhesive layer.
- the amount of the dye to be used can be reduced, and the manufacturing cost of the laminate can be reduced.
- a multilayer film can be manufactured by bonding an adhesive layer and an airtight layer.
- the adhesive layer and the hermetic layer can be formed in advance as separate sheets or films by extrusion or the like, and joined together to be integrated.
- the method include a method in which each sheet or film is stacked and melt-pressed by a hot press or a heat roll, and an extrusion laminating method in which a molten material is extruded onto a formed sheet or film.
- each layer of the adhesive layer and the hermetic layer can be respectively melted and simultaneously extruded and molded using, for example, an inflation molding method or a T-die method.
- an inflation method that can increase the area and is excellent in productivity.
- the multilayer film according to the present embodiment is used by being adhered to a base fabric.
- the base fabric is a sheet-like structure functioning as a support for securing the strength of a laminate as a final product, obtained by laminating a multilayer film and a base fabric.
- the sheet shape includes a shape formed in a cylindrical shape, a bag shape, and a balloon shape in addition to a planar shape.
- the base fabric preferably includes fibers, and may be a woven fabric, a knitted fabric, or a non-woven fabric, and may be sewn entirely or partially.
- a woven fabric is preferable, and a biaxial structure in which a plurality of warps and a plurality of wefts are combined is preferable, and a combination of a plurality of warps, a plurality of wefts, and a plurality of oblique yarns is combined.
- a triaxial structure can also be used.
- a biaxial base fabric is preferable, and a plain woven fabric is more preferable in terms of strength and ease of manufacture.
- the base fabric is not a flat base fabric, but also an OPW (One Piece Woven) that is woven into a bag shape without a seam so that it can have a curved surface according to the shape of the target product. included.
- OPW One Piece Woven
- the OPW can be suitably used for applications such as airbags that are used by inflating and storing air inside.
- the OPW used for the curtain airbag may have a complicated curved surface in which a plurality of rooms are formed, and a structure in which irregularities are formed when inflated.
- peeling between the base fabric and the film is more likely to occur than when a film is adhered to a base fabric without undulations.
- the multilayer film according to the present embodiment the multilayer film can be satisfactorily adhered even if it is an uneven OPW, and delamination can be prevented.
- the fibers contained in the base fabric may be synthetic fibers, natural fibers, regenerated fibers, semi-synthetic fibers, inorganic fibers, and combinations thereof (including mixed spinning and blending).
- synthetic fibers particularly polymer fibers are preferable.
- composite fibers such as core-sheath fibers, side-by-side fibers, and split fibers can be used.
- polymer constituting the fiber examples include homopolyesters such as polyalkylene terephthalate such as polyethylene terephthalate and polybutylene terephthalate, and aliphatic dicarboxylic acids such as isophthalic acid, 5-sodium sulfoisophthalic acid and adipic acid as the acid component constituting the polyester repeating unit Polyester fiber copolymerized with acid, nylon 6,6, nylon 6, nylon 12, nylon 4,6, nylon 6 and nylon 6,6 copolymer, nylon with polyalkylene glycol, dicarboxylic acid, amines, etc.
- homopolyesters such as polyalkylene terephthalate such as polyethylene terephthalate and polybutylene terephthalate
- aliphatic dicarboxylic acids such as isophthalic acid, 5-sodium sulfoisophthalic acid and adipic acid as the acid component constituting the polyester repeating unit Polyester fiber copolymerized with acid, nylon 6,6, nylon 6, nylon 12, nylon 4,6, nylon
- Polymerized polyamide fiber Polymerized polyamide fiber, aramid fiber represented by copolymerization with paraphenylene terephthalamide and aromatic ether, rayon fiber, ultrahigh molecular weight polyethylene fiber, paraphenylene sulfone, polysulfone, etc. Sulfone fibers, polyether ketone fibers and the like.
- the base fabric when the base fabric is a woven fabric, the base fabric may include two or more fibers.
- different types of fibers can be used as fibers used for yarns extending in different directions. More specifically, when having a biaxial structure including a warp and a weft, the warp and the weft can be different types of fibers. In this case, at least one of the warp and the weft can be a polyester fiber.
- the multilayer film according to the present embodiment can be suitably used for lamination on a base fabric containing polyester fibers.
- the base fabric is preferably formed using a yarn having a total fineness (single yarn fineness ⁇ number of combined yarns) of 100 to 700 dtex.
- the single yarn fineness of the fiber used for the base fabric is preferably 1 to 10 dtex.
- the weaving density is preferably 5 to 30 yarns / cm 2 for warps and wefts.
- the basis weight (weight per 1 m 2 ) of the base fabric is 300 g / m 2 or less, more preferably 200 g / m 2 or less, and even more preferably 190 g / m 2 in consideration of the storage property and cost of the laminate (final product).
- it is more preferably 150 g / m 2 or less and 100 g / m 2 or less.
- Preferably it is 30 g / m ⁇ 2 > or more, More preferably, it is 50 g / m ⁇ 2 > or more, More preferably, it can be 70 g / m ⁇ 2 > or more.
- FIG. 2 is a schematic cross-sectional view of a laminate according to an embodiment of the present invention.
- the laminated body 5 is configured by adhering the multilayer film 1 including the airtight layer 2 and the adhesive layer 3 described above and the base fabric 4 to each other.
- the multilayer film 1 is disposed on one surface of the base fabric 4, but the multilayer film of this embodiment can also be provided on both surfaces of the base fabric 4. Further, when OPW folded into a bag shape without a seam is used as the base fabric, as shown in FIG. 3, the multilayer films 1a and 1b may be laminated on the surface from above and below, respectively. Good. The laminate shown in FIG. 3 can be used for an airbag or the like.
- One aspect of the present invention is a method for producing a laminate having the above-described multilayer film and a base fabric, and heating the multilayer film to a base fabric on the adhesive layer side while heating at a temperature below the melting point of the hermetic layer. A step of bonding.
- film means a flexible thin film, and its temperature, hardness, etc. are not limited. That is, the supplied multilayer film may be at room temperature or lower, or may be at a temperature higher than room temperature. Further, it may be softened and at least partially capable of exhibiting an adhesive function. Therefore, the laminate according to the present embodiment can be produced, for example, by adhering a multilayer film supplied at room temperature or lower to a base fabric while heating at a temperature lower than the melting point of the hermetic layer using a heating means. Also, for example, the polymer heated in an extruder and extruded into a film can be produced by adhering to a base fabric.
- FIG. 4 schematically shows a laminate manufacturing apparatus 20 for carrying out the laminate manufacturing method according to the present embodiment.
- stacked on both surfaces of the base fabric 4 is demonstrated.
- the laminate manufacturing apparatus 20 includes a heating unit 22 and a cooling unit 24.
- the base fabric 4 and the multilayer films 1a and 1b previously wound on a reel or the like are unwound, and both surfaces (upper surface) of the base fabric 4 are unwound.
- Multilayer films 1a and 1b are overlaid on the lower surface and the lower surface, respectively.
- the laminated multilayer film 1b, the base cloth 4, and the multilayer film 1a are sent to the heating unit 22 and pressed while being heated in the heating unit 22.
- the heating unit 22 includes, for example, a pressurizing unit composed of a pair of opposed rolls (such as a nip roll) or a pair of opposed belts as in the illustrated example. And heating and pressurization can be performed by passing the laminated multilayer film 1b, the base fabric 4, and the multilayer film 1a between such a pair of pressurizing means.
- the melting point of the adhesive layer of the multilayer film is a temperature lower than the melting point of the hermetic layer
- the adhesive layer is sufficiently softened. With this, the adhesive layer can be pressed onto the base fabric.
- multilayer film 1a, 1b can be adhere
- the laminate 5 that has passed through the heating unit 22 is sent to the cooling unit 24.
- the temperature of the laminated body 5 can be preferably lowered to room temperature.
- the cooling unit 24 may include a cooling unit including a cooling medium, an intake unit, and the like. Further, in the cooling unit 24, as shown in the illustrated example, the pressure may be applied using a pressurizing unit including a pair of opposed belts, but the pressurization is not necessarily required.
- a laminate in which the multilayer film 1 is laminated on one side of the base fabric 4 as shown in FIG. 2 can be manufactured. it can.
- the base cloth 4 a tubular or bag-like OPW woven without a seam can be used. Thereby, a laminated body as shown in FIG. 3 can be manufactured.
- the base fabric 4 is made into a sheet shape by removing air from the inside of the bag-shaped base fabric 4, wound beforehand on a reel or the like, and unrolled before being overlapped. Then, the multilayer films 1a and 1b are overlaid on the upper and lower surfaces of the base fabric 4 as described above. In this case, since the base fabric 4 has a bag shape, the upper surface and the lower surface of the base fabric 4 are both the surface of the base fabric 4.
- FIG. 5 schematically shows a state in which the multilayer films 1a and 1b are overlaid on the upper and lower surfaces of the base fabric 4 put into the laminate manufacturing apparatus 20 in a flattened state.
- the multilayer film 1a having the airtight layer 2a and the adhesive layer 3a is overlapped so that the adhesive layer 3a is on the base cloth 4 side.
- the multilayer film 1b having the airtight layer 2b and the adhesive layer 3b is overlapped so that the adhesive layer 3b is on the base cloth 4 side.
- the multilayer film 1a, the base fabric 4, and the multilayer film 1b which were overlaid as shown in FIG. 5 are pressurized from both surfaces in a pressurization part 22 by a pair of pressurization means.
- the multilayer films 1a and 1b are respectively joined to the upper surface and the lower surface of the base fabric 4, and the edges of the multilayer films 1a and 1b are joined to each other by heating or by an adhesive.
- a laminate (airbag) 6 can be obtained. Excess edges may be cut off. In this manner, an airbag in which the base fabric is formed in a bag shape and the multilayer film is formed on the surface of the base fabric can be manufactured.
- the heating temperature at the time of manufacturing the laminate is not particularly limited as long as the temperature is lower than the melting point of the hermetic layer.
- the heating temperature can be a temperature below the melting point of the hermetic layer and a temperature at which the adhesive layer softens. Specifically, the temperature is preferably 120 to 250 ° C.
- the pressurizing pressure may be 5 to 700 N / cm 2 , preferably 10 to 500 N / cm 2 , although it depends on the configuration of the multilayer film and the base fabric. Furthermore, it can be set to 5 to 50 N / cm 2 depending on the operating conditions at the time of manufacturing the laminate.
- the multilayer film and laminate according to the present embodiment are suitably used in vehicle airbags, outdoor products, packaging applications, and the like, and particularly suitable for the production of vehicle airbags, especially curtain airbags.
- the curtain airbag refers to an airbag that is attached to a roof line or the like on the upper side of a side window and is deployed in a curtain shape vertically downward along the side window when a high load is applied during a collision or the like.
- curtain airbag Since the curtain airbag is inflated for several seconds after operation, for example, 6 to 7 seconds, when deployed, the curtain airbag material is required to have pressure resistance. Further, curtain airbags are often stored in a casing or the like in a folded or rolled state for a long time before deployment, and are often exposed to high temperature and high humidity environments.
- the multilayer film and laminate according to the present embodiment can be suitably used even for such applications.
- a multilayer film including an airtight layer and an adhesive layer was formed, and the multilayer film was bonded to a base fabric to produce a laminate and evaluated.
- Thermoplastic polyester elastomer (PTEE-1): A polyester-polyether block copolymer having polybutylene terephthalate as a hard segment and polytetramethylene ether glycol having a number average molecular weight of 2000 as a soft segment. In the copolymer, the content of polybutylene terephthalate is 28% by weight, and the content of polytetramethylene ether glycol segment is 72% by weight (melting point 160 ° C.).
- Thermoplastic polyester elastomer (PTEE-2): A polyester-polyether block copolymer having polybutylene terephthalate as a hard segment and polytetramethylene ether glycol having a number average molecular weight of 2000 as a soft segment.
- PTEE-2 Thermoplastic polyester elastomer
- the content of polybutylene terephthalate is 58% by weight
- the content of polytetramethylene ether glycol segment is 42% by weight (melting point 207 ° C.).
- Ethylene-vinyl acetate copolymer (EVA): “Evatan (registered trademark) 2805” manufactured by Arkema Co., Ltd., Shore D hardness 15-40 Polyethylene (PE): “PG7004” manufactured by Dow Chemical Company (low density polyethylene), Shore D hardness 45-55 Hydrogenated Styrenic Thermoplastic Elastomer (SEBS): “Tuftec” manufactured by Asahi Kasei Co., Ltd., Shore A hardness of 40 or less (corresponding to Shore D hardness of about 8 or less) Ethylene-butyl acrylate copolymer resin (EBA): “Elvaoly” manufactured by Du Pont, Shore D hardness 30-50 Polymethyl methacrylate resin: “ACRYPET” manufactured by Mitsubishi Rayon Co., Ltd., Shore D hardness 80-100
- the peeling force was more than 0.5 N / mm.
- ⁇ The peel strength was 0.3 to 0.5 N / mm.
- X The peeling force was less than 0.3 N / mm, or delamination occurred in the multilayer film.
- a polyethylene terephthalate film having a thickness of 100 ⁇ m is bonded to the airtight layer side of the multilayer film with an adhesive to prevent the multilayer film from being broken or stretched during the peel test. Reinforced and used.
- Example 1 (Multilayer film) The multilayer film was manufactured using the inflation extrusion apparatus (made by Dr Collin) which has three extruders. In each extruder, a mixture of 70% by weight of thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA), thermoplastic polyester elastomer (PTEE-1), and heat A plastic polyester elastomer (PTEE-2) was added and melted at a temperature equal to or higher than the melting point of each raw material to prepare a three-layer film by an inflation method.
- PTEE-1 thermoplastic polyester elastomer
- EVA ethylene-vinyl acetate copolymer
- PTEE-1 thermoplastic polyester elastomer
- PTEE-2 thermoplastic polyester elastomer
- the obtained film is composed of a first adhesive layer composed of a mixture of 70% by weight of a thermoplastic polyester elastomer (PTEE-1) and 30% by weight of an ethylene-vinyl acetate copolymer (EVA), a thermoplastic polyester elastomer (TEE-1) and the airtight layer made of the thermoplastic polyester elastomer (PTEE-2) were a three-layer film laminated in this order.
- the extrusion amounts of the first adhesive layer, the second adhesive layer, and the airtight layer were each 10 g / m 2 .
- a plain woven base fabric woven with polyethylene terephthalate fibers was used as the base fabric.
- the total fineness of the warp and weft was 470 dtex, and the weaving density was 22 / cm for each of the warp and the weft.
- the PET base fabric and the three-layer film are laminated so that the adhesive layer is in contact with the surface of the base fabric, heated at 170 ° C., and heated with a nip roll. While pressing to 18 N / cm 2 , the adhesive layer was softened, and a base fabric and a three-layer film were laminated.
- Example 2 (Multilayer film) Instead of a mixture of 70% by weight of thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA), 70% by weight of thermoplastic polyester elastomer (PTEE-1) and polyethylene A three-layer film was produced in the same manner as in Example 1 except that a mixture of (PE) 30% by weight was used.
- PTEE-1 thermoplastic polyester elastomer
- EVA ethylene-vinyl acetate copolymer
- the obtained film includes a first adhesive layer made of thermoplastic polyester elastomer (PTEE-1) and polyethylene (PE), a second adhesive layer made of thermoplastic polyester elastomer (PTEE-1), and a heat
- PTEE-2 thermoplastic polyester elastomer
- the airtight layer made of the plastic polyester elastomer (PTEE-2) was a three-layer film laminated in this order.
- Example 3 In place of a mixture of 70% by weight of thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA), 70% by weight of thermoplastic polyester elastomer (PTEE-1), A three-layer film was produced in the same manner as in Example 1 except that a mixture of 15% by weight of polyethylene (PE) and 15% by weight of hydrogenated styrene thermoplastic elastomer (SEBS) was used.
- PE polyethylene
- SEBS hydrogenated styrene thermoplastic elastomer
- the obtained film is composed of a first adhesive layer composed of a thermoplastic polyester elastomer (PTEE-1), polyethylene (PE) and a hydrogenated styrene thermoplastic elastomer (SEBS), a thermoplastic polyester elastomer (PTEE-1). ) And a hermetic layer made of a thermoplastic polyester elastomer (PTEE-2) were three-layer films laminated in this order.
- PTEE-1 thermoplastic polyester elastomer
- PE polyethylene
- SEBS hydrogenated styrene thermoplastic elastomer
- PTEE-1 thermoplastic polyester elastomer
- SEBS hydrogenated styrene thermoplastic elastomer
- PTEE-1 polyethylene
- SEBS hydrogenated styrene thermoplastic elastomer
- PTEE-1 polyethylene
- SEBS hydrogenated styrene thermoplastic elastomer
- PTEE-1 polyethylene
- SEBS hydrogenated styrene thermoplastic
- thermoplastic polyester elastomer (PTEE-1) In place of a mixture of 70% by weight of thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA), 70% by weight of thermoplastic polyester elastomer (PTEE-1), A three-layer film was produced in the same manner as in Example 1 except that a mixture with 30% by weight of hydrogenated styrene-based thermoplastic elastomer (SEBS) was used.
- SEBS hydrogenated styrene-based thermoplastic elastomer
- the obtained film has a first adhesive layer composed of a thermoplastic polyester elastomer (PTEE-1) and a hydrogenated styrene thermoplastic elastomer (SEBS), and a second adhesive layer composed of a thermoplastic polyester elastomer (PTEE-1).
- an airtight layer made of a thermoplastic polyester elastomer (PTEE-2) was a three-layer film laminated in this
- thermoplastic polyester elastomer (PTEE-1) In place of a mixture of 70% by weight of thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA), 70% by weight of thermoplastic polyester elastomer (PTEE-1), A three-layer film was produced in the same manner as in Example 1 except that a mixture with 30% by weight of ethylene-butyl acrylate copolymer resin (EBA) was used.
- the obtained film has a first adhesive layer composed of a thermoplastic polyester elastomer (PTEE-1) and an ethylene-butyl acrylate copolymer resin (EBA), and a second adhesive layer composed of a thermoplastic polyester elastomer (PTEE-1).
- an airtight layer made of a thermoplastic polyester elastomer (PTEE-2) was a three-layer film laminated in this order.
- thermoplastic polyester elastomer (PTEE-1) instead of a mixture of 70% by weight of thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA), 100% by weight of thermoplastic polyester elastomer (PTEE-1) was used.
- a three-layer film was produced in the same manner as Example 1 except for the above.
- the obtained film includes a first adhesive layer made of a thermoplastic polyester elastomer (PTEE-1), a second adhesive layer made of a thermoplastic polyester elastomer (PTEE-1), and a thermoplastic polyester elastomer (PTEE).
- PTEE-1 thermoplastic polyester elastomer
- PTEE-1 thermoplastic polyester elastomer
- PTEE-1 thermoplastic polyester elastomer
- PTEE-1 thermoplastic polyester elastomer
- PTEE-1 thermoplastic polyester elastomer
- PTEE-1 thermoplastic polyester elastomer
- PTEE thermo
- thermoplastic polyester elastomer (PTEE-1) and 30% by weight of ethylene-vinyl acetate copolymer (EVA) 70% by weight of thermoplastic polyester elastomer (PTEE-1) and polymethacrylic
- PTEE-1 and polymethacrylic A three-layer film was prepared in the same manner as in Example 1 except that a mixture with 30% by weight of acid methyl resin (PMMA) was used.
- the obtained film has a first adhesive layer made of thermoplastic polyester elastomer (PTEE-1) and polymethyl methacrylate resin (PMMA), and a second adhesive made of ethylene-vinyl acetate copolymer (EVA).
- the layer and the hermetic layer made of the thermoplastic polyester elastomer (PTEE-2) were a three-layer film laminated in this order.
- the laminates of Examples 1 to 5 having an adhesive layer containing a thermoplastic polyester elastomer and a polymer having a Shore D hardness of less than 80 have excellent adhesiveness under high temperature and high humidity, and flexibility. And can be manufactured at low cost.
- Examples 1 to 5 were particularly excellent in terms of cost.
- Appendix 1 A multilayer film used by bonding to a base fabric, An adhesive layer to be bonded to the base fabric, and an airtight layer bonded to the adhesive layer;
- Appendix 2 The multilayer film according to appendix 1, wherein a melting point of the airtight layer is higher than a melting point of the adhesive layer.
- thermoplastic polyester elastomer in the adhesive layer is a block copolymer including a soft segment including a polyether and a hard segment including a polyester.
- Appendix 4 The multilayer film according to any one of appendices 1 to 3, wherein the airtight layer includes a thermoplastic polyester elastomer.
- Appendix 7 A laminate comprising the multilayer film according to any one of appendices 1 to 6 and a base fabric bonded together.
- Appendix 8 An airbag using the laminate according to appendix 7, An airbag in which the base fabric is formed in a bag shape, and the multilayer film is formed on a surface of the base fabric.
- Appendix 9 A method for producing a laminate having the multilayer film according to any one of appendices 1 to 6 and a base fabric, A manufacturing method comprising the step of adhering the multilayer film to the base fabric on the side of the adhesive layer while heating at a temperature lower than the melting point of the hermetic layer.
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- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Textile Engineering (AREA)
- Laminated Bodies (AREA)
- Air Bags (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Abstract
Description
図1に、多層フィルム1の模式的な断面図を示す。本発明の一態様は、図1に示すように、多層フィルム1であって、気密層2と、この気密層2に接合されている接着層3とを有する。当該多層フィルム1は、基布に接着させて使用されるものであり、接着層3は、基布に接着される側となる。
接着層は、熱可塑性ポリエステル系エラストマーと、ショアD硬度80未満のポリマーとを含む。この組成により、得られる積層体の耐層間剥離性を、低コストで向上させることができる。すなわち、接着層と基布との接着性及び接着層と気密層との接着性を、常温においても、高温及び/又は高湿の条件下でも向上させることができる。また、積層体全体の柔軟性や機械的強度をバランス良く向上させることができる。
気密層を構成する材料は、特に限定されないが、熱可塑性エラストマーを用いることが好ましい。熱可塑性エラストマーとしては、ポリアミド系エラストマー、ポリオレフィン系エラストマー、ポリウレタン系エラストマー、ポリスチレン系エラストマー、ポリブタジエン系エラストマー等が挙げられる。上記のうち、接着層に含まれる熱可塑性エラストマーと同系のエラストマーであること等から、気密層にも熱可塑性ポリエステル系エラストマーを用いることが好ましい。気密層及び接着層の両層にポリエステル系のエラストマーが含まれていることで、接着層と気密層との接着性(耐層間剥離性)を、常温においても、高温及び/又は高湿の条件下においても向上させることができる。
上述のように、多層フィルムは、気密層と接着層とを有している。接着層は、1層であってもよいし複数であってもよい。接着層が複数ある場合には、各接着層を構成する材料は、同じであってもよく、異なっていてもよい。また、複数の接着層の各層の融点は、同じであってもよいし異なっていてもよい。気密層も、同様に、1層であってもよいし、複数であってもよい。気密層が複数ある場合には、各気密層を構成する材料及び融点もそれぞれ、同じであってもよいし異なっていてもよい。
本形態による多層フィルムは、基布に接着させて使用するものである。本明細書において、基布とは、多層フィルムと基布との積層により得られる、最終製品である積層体の強度を確保するための支持体として機能するシート状の構造体である。ここで、シート状とは、平面状の他、筒状、袋状、風船状に形成された形状も含む。
図2に、本発明の一形態による積層体の模式的な断面図を示す。積層体5は、上述した気密層2と接着層3とを備えた多層フィルム1と、基布4とが互いに接着されて構成されている。
本発明の一形態は、上述の多層フィルムと、基布とを有する積層体の製造方法であって、気密層の融点を下回る温度で加熱しながら、多層フィルムを接着層の側で基布に接着させる工程を含む。
本形態による多層フィルム及び積層体は、車両用エアバッグ、アウトドア用品、包装用途等において好適に用いられ、特に車両用エアバッグ、とりわけカーテンエアバッグの製造に好適に用いられる。カーテンエアバッグとは、サイドウインドウ上部のルーフライン等に取り付けられており、衝突時等に高荷重が作用した場合に、サイドウインドウに沿わせて鉛直下方にカーテン状に展開させるエアバッグを指す。
多層フィルムの原料として、以下のものを使用した。なお、各原料の融点は、示差走査熱量計で測定された融解ピーク温度である。
熱可塑性ポリエステル系エラストマー(PTEE-1):ポリブチレンテレフタレートをハードセグメントとし、数平均分子量2000のポリテトラメチレンエーテルグリコールをソフトセグメントとする、ポリエステル-ポリエーテルブロック共重合体。上記共重合体中、ポリブチレンテレフタレートの含有割合が28重量%であり、ポリテトラメチレンエーテルグリコールセグメントの含有割合が72重量%である(融点160℃)
エチレン-酢酸ビニル共重合体(EVA):「Evatan(登録商標)2805」アルケマ株式会社製、ショアD硬度15~40
ポリエチレン(PE):「PG7004」ダウケミカル社製(低密度ポリエチレン)、ショアD硬度45~55
水添スチレン系熱可塑性エラストマー(SEBS):「タフテック」旭化成株式会社製、ショアA硬度40以下(ショアD硬度約8以下に相当)
エチレン‐ブチルアクリレート共重合樹脂(EBA):「Elvaoly」Du Pont社製、ショアD硬度30~50
ポリメタクリル酸メチル樹脂:「アクリペット」三菱レイヨン株式会社製、ショアD硬度80~100
<高温高湿接着性(高温高湿下での耐層間剥離性)>
多層フィルムと基布とを後述のように接着させて得られた積層体から、50mm×150mmの試験片を作製し、この試験片を密閉容器内に入れ、容器内の条件を温度70℃、相対湿度95%にして408時間にわたり保った。容器から取り出した試験片(積層体)の基布の部分を固定しつつ、多層フィルムの部分(気密層及び接着層)を180°方向に引張速度100mm/分で引きはがした際に要した力を剥離力(N/mm)として測定した。評価基準は以下の通りである。
〇:剥離力が0.5N/mm超であった。
△:剥離力が0.3~0.5N/mmであった。
×:剥離力が0.3N/mm未満であった、又は多層フィルム内で層間剥離が生じた。
(多層フィルム)
3つの押出機を有するインフレーション押出装置(Dr Collin社製)を用いて多層フィルムの製造を行った。各押出機にそれぞれ、熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)30重量%との混合物、熱可塑性ポリエステル系エラストマー(PTEE-1)、及び熱可塑性ポリエステル系エラストマー(PTEE-2)を投入し、各原料の融点以上で溶融し、インフレーション法にて3層フィルムを作製した。
基布として、ポリエチレンテレフタレート製の繊維で織られた平織基布を使用した。経糸及び緯糸の総繊度はいずれも470dtexであり、織り密度は、経糸及び緯糸それぞれ22本/cmであった。
(多層フィルム)
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)と30重量%との混合物に代えて、熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とポリエチレン(PE)30重量%との混合物を用いたこと以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、熱可塑性ポリエステル系エラストマー(PTEE-1)とポリエチレン(PE)とからなる第1の接着層、熱可塑性ポリエステル系エラストマー(PTEE-1)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)と30重量%との混合物に代えて、熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%と、ポリエチレン(PE)15重量%と、水添スチレン系熱可塑性エラストマー(SEBS)15重量%との混合物を用いたこと以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、熱可塑性ポリエステル系エラストマー(PTEE-1)とポリエチレン(PE)と水添スチレン系熱可塑性エラストマー(SEBS)とからなる第1の接着層、熱可塑性ポリエステル系エラストマー(PTEE-1)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)と30重量%との混合物に代えて、熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%と、水添スチレン系熱可塑性エラストマー(SEBS)30重量%との混合物を用いたこと以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、熱可塑性ポリエステル系エラストマー(PTEE-1)と水添スチレン系熱可塑性エラストマー(SEBS)とからなる第1の接着層、熱可塑性ポリエステル系エラストマー(PTEE-1)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)と30重量%との混合物に代えて、熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%と、エチレン-ブチルアクリレート共重合樹脂(EBA)30重量%との混合物を用いたこと以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、熱可塑性ポリエステル系エラストマー(PTEE-1)とエチレン-ブチルアクリレート共重合樹脂(EBA)とからなる第1の接着層、熱可塑性ポリエステル系エラストマー(PTEE-1)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
(多層フィルム)
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)30重量%との混合物に代えて、熱可塑性ポリエステル系エラストマー(PTEE-1)100重量%を用いた以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、熱可塑性ポリエステル系エラストマー(PTEE-1)からなる第1の接着層、熱可塑性ポリエステル系エラストマー(PTEE-1)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
(多層フィルム)
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)30重量%との混合物に代えて、エチレン-酢酸ビニル共重合体(EVA)100重量%を用いた以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、エチレン-酢酸ビニル共重合体(EVA)からなる第1の接着層、エチレン-酢酸ビニル共重合体(EVA)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
(多層フィルム)
熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とエチレン-酢酸ビニル共重合体(EVA)30重量5との混合物に代えて、熱可塑性ポリエステル系エラストマー(PTEE-1)70重量%とポリメタクリル酸メチル樹脂(PMMA)30重量%との混合物を用いた以外は、実施例1と同様にして3層フィルムを作製した。得られたフィルムは、熱可塑性ポリエステル系エラストマー(PTEE-1)とポリメタクリル酸メチル樹脂(PMMA)とからなる第1の接着層、エチレン-酢酸ビニル共重合体(EVA)からなる第2の接着層、及び熱可塑性ポリエステル系エラストマー(PTEE-2)からなる気密層が、この順に積層された3層フィルムであった。
実施例1と同様にして、基布と多層フィルムの積層体を作製し、評価を行った。結果を表1に示す。
以下、本発明の好ましい実施形態を付記する。
基布に接着して使用される多層フィルムであって、
前記基布に接着される側となる接着層と、当該接着層に接合されている気密層とを有し、
前記接着層が、熱可塑性ポリエステル系エラストマーと、エチレン-酢酸ビニル共重合体とを含む、多層フィルム。
前記気密層の融点が、前記接着層の融点よりも高い、付記1に記載の多層フィルム。
前記接着層中の熱可塑性ポリエステル系エラストマーが、ポリエーテルを含むソフトセグメントと、ポリエステルを含むハードセグメントとを含むブロック共重合体である、付記1又は2に記載の多層フィルム。
前記気密層が、熱可塑性ポリエステル系エラストマーを含む、付記1から3のいずれかに記載の多層フィルム。
前記基布がポリエステルを含む、付記1から4のいずれかに記載の多層フィルム。
前記基布がエアバッグ用基布である、付記1から5のいずれかに記載の多層フィルム。
付記1から6のいずれか一項に記載の多層フィルムと、基布とが接着されてなる、積層体。
付記7に記載の積層体を用いてなるエアバッグであって、
前記基布が袋状に形成されており、前記基布の表面に前記多層フィルムが形成されている、エアバッグ。
付記1から6のいずれかに記載の多層フィルムと、基布とを有する積層体の製造方法であって、
前記気密層の融点を下回る温度で加熱しながら、前記多層フィルムを前記接着層の側で前記基布に接着させる工程を含む、製造方法。
2、2a、2b 気密層
3、3a、3b 接着層
4 基布
5 積層体
6 積層体(エアバッグ)
20 積層体製造装置
22 加熱部
24 冷却部
Claims (10)
- 基布に接着して使用される多層フィルムであって、
前記基布に接着される側となる接着層と、当該接着層に接合されている気密層とを有し、
前記接着層が、熱可塑性ポリエステル系エラストマーと、ショアD硬度80未満のポリマーとを含む、多層フィルム。 - 前記ショアD硬度80未満のポリマーが、エチレン-酢酸ビニル共重合体、ポリエチレン、水添スチレン系熱可塑性エラストマー、エチレン-ブチルアクリレート共重合体のうち1種以上である、請求項1に記載の多層フィルム。
- 前記気密層の融点が、前記接着層の融点よりも高い、請求項1又は2に記載の多層フィルム。
- 前記接着層中の熱可塑性ポリエステル系エラストマーが、ポリエーテルを含むソフトセグメントと、ポリエステルを含むハードセグメントとを含むブロック共重合体である、請求項1から3のいずれか一項に記載の多層フィルム。
- 前記気密層が、熱可塑性ポリエステル系エラストマーを含む、請求項1から4のいずれか一項に記載の多層フィルム。
- 前記基布がポリエステルを含む、請求項1から5のいずれか一項に記載の多層フィルム。
- 前記基布がエアバッグ用基布である、請求項1から6のいずれか一項に記載の多層フィルム。
- 請求項1から7のいずれか一項に記載の多層フィルムと、基布とが接着されてなる、積層体。
- 請求項8に記載の積層体を用いてなるエアバッグであって、
前記基布が袋状に形成されており、前記基布の表面に前記多層フィルムが形成されている、エアバッグ。 - 請求項1から7のいずれか一項に記載の多層フィルムと、基布とを有する積層体の製造方法であって、
前記気密層の融点を下回る温度で加熱しながら、前記多層フィルムを前記接着層の側で前記基布に接着させる工程を含む、製造方法。
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KR1020197036762A KR102288992B1 (ko) | 2017-06-16 | 2018-06-15 | 다층 필름, 적층체, 에어백 및 적층체 제조방법 |
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CN201880039675.3A CN110944842B (zh) | 2017-06-16 | 2018-06-15 | 多层膜、叠层体、安全气囊以及叠层体的制造方法 |
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EP (1) | EP3640026B1 (ja) |
JP (1) | JP6898276B2 (ja) |
KR (1) | KR102288992B1 (ja) |
CN (1) | CN110944842B (ja) |
CA (1) | CA3067202A1 (ja) |
MX (1) | MX2019014946A (ja) |
WO (1) | WO2018230722A1 (ja) |
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WO2021112202A1 (ja) * | 2019-12-06 | 2021-06-10 | 日東電工株式会社 | 多層フィルム、積層体及びエアバッグ |
WO2021151892A1 (en) * | 2020-01-27 | 2021-08-05 | Dsm Ip Assets B.V. | Layered material |
Families Citing this family (1)
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KR20210103090A (ko) | 2020-02-13 | 2021-08-23 | 주식회사 엘지에너지솔루션 | 레일형 소켓이 구비된 전지 모듈 및 이를 포함하는 전지 팩 |
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Cited By (6)
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WO2021112202A1 (ja) * | 2019-12-06 | 2021-06-10 | 日東電工株式会社 | 多層フィルム、積層体及びエアバッグ |
US11745481B2 (en) | 2019-12-06 | 2023-09-05 | Zf Automotive Germany Gmbh | Multilayer film, laminated body, and air bag |
EP4070951A4 (en) * | 2019-12-06 | 2023-12-06 | ZF Automotive Germany GmbH | MULTI-LAYER FILM, LAMINATE AND AIRBAG |
WO2021151892A1 (en) * | 2020-01-27 | 2021-08-05 | Dsm Ip Assets B.V. | Layered material |
CN114929471A (zh) * | 2020-01-27 | 2022-08-19 | 帝斯曼知识产权资产管理有限公司 | 层状材料 |
CN114929471B (zh) * | 2020-01-27 | 2024-02-20 | 帝斯曼知识产权资产管理有限公司 | 层状材料 |
Also Published As
Publication number | Publication date |
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KR20200017410A (ko) | 2020-02-18 |
EP3640026A1 (en) | 2020-04-22 |
JP2019001163A (ja) | 2019-01-10 |
US11072152B2 (en) | 2021-07-27 |
EP3640026B1 (en) | 2022-07-27 |
EP3640026A4 (en) | 2020-07-08 |
CN110944842A (zh) | 2020-03-31 |
JP6898276B2 (ja) | 2021-07-07 |
US20200114631A1 (en) | 2020-04-16 |
CA3067202A1 (en) | 2018-12-20 |
CN110944842B (zh) | 2022-10-25 |
KR102288992B1 (ko) | 2021-08-12 |
MX2019014946A (es) | 2020-08-06 |
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