WO1999064533A1 - Films adhesifs a couches multiples - Google Patents
Films adhesifs a couches multiples Download PDFInfo
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- WO1999064533A1 WO1999064533A1 PCT/US1999/012789 US9912789W WO9964533A1 WO 1999064533 A1 WO1999064533 A1 WO 1999064533A1 US 9912789 W US9912789 W US 9912789W WO 9964533 A1 WO9964533 A1 WO 9964533A1
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- Prior art keywords
- film
- adhesive
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- core layer
- polymer
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Classifications
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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
-
- 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
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
- B32B5/022—Non-woven fabric
-
- 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
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/22—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
- B32B5/24—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
- B32B5/245—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it being a foam layer
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
- C09J7/24—Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/241—Polyolefin, e.g.rubber
- C09J7/243—Ethylene or propylene polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/35—Heat-activated
-
- 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
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/02—Composition of the impregnated, bonded or embedded layer
- B32B2260/021—Fibrous or filamentary layer
-
- 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
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/04—Impregnation, embedding, or binder material
- B32B2260/046—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
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/10—Inorganic fibres
- B32B2262/101—Glass fibres
-
- 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
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
- B32B2266/0214—Materials belonging to B32B27/00
- B32B2266/0278—Polyurethane
-
- 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
- B32B2405/00—Adhesive articles, e.g. adhesive tapes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
- C09J2301/124—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present on both sides of the carrier, e.g. double-sided adhesive tape
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/304—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being heat-activatable, i.e. not tacky at temperatures inferior to 30°C
Definitions
- This invention relates to adhesive films.
- Thermoplastic adhesive films are frequently used to bond together various layers of automotive interior panels, such as headliners and visors.
- the thermoplastic adhesive films can be used to impart thermoformability to, or enhance thermoformability of, such laminates.
- the adhesive film helps retain a desired shape of an automobile interior panel after the laminate has been subjected to thermoforming. This is particularly important in situations where the laminate is free of thermosettable resins and rigid foam.
- the thermoplastic film should remain relatively stiff at temperatures in excess of those which may be generated in a closed vehicle on a sunny day, to prevent sagging of the automobile interior panel (e.g., headiiner) under such conditions.
- thermoformable laminates for automobile interior panels tend to have excellent adhesive properties. Although the stiffness of such monolayer adhesive films is acceptable for many applications, it would be desirable to provide an adhesive film for use in thermoformable laminates for making automobile interior panels that has both excellent adhesive properties and improved stiffness to impart excellent anti-sag properties to automobile interior panels, even at highly elevated (abuse) temperatures.
- a liquid thermosettable adhesive composition e.g., poiyurethane adhesive system
- thermoformable laminates for automobile interior panel applications which exhibits enhanced elongation, extensibility, and improved tear strength in addition to excellent adhesive properties like those of conventional multipurpose monolayer adhesive films and, desirably, improved stiffness (e.g., higher modulus).
- the multiple layer adhesive films of this invention have higher moduli than conventional monolayer adhesive films, and, therefore, impart improved sag resistance at elevated temperatures to laminated structures that are bonded together with these adhesive films.
- the multiple layer adhesive films also exhibit enhanced elongation, extensibility, and improved tear resistance, thus providing excellent barrier properties when used to bond together various layers of formed laminar articles of manufacture including automotive interior panels, such as headliners, other automotive applications, such as trunk liners, and any of a variety of non-automotive end uses.
- the formed laminar articles are preferably prepared via conventional thermoforming procedures that include use of a closed mold with temperatures in excess of 300° Fahrenheit (148.9°C) and pressures of from 10 psi (68.9 kilopascals (KPa)) up to and including 60 psi (413.7 KPa).
- KPa kilopascals
- the multiple layer adhesive films of this invention comprise a core layer having a first side and an opposing second side; a first outer adhesive layer bonded to the first side of the core layer; a second outer adhesive layers bonded to the second side of the core layer; the adhesive layers each comprising a polymer blend including an ethylene homopolymer and an ethylene copolymer having polar moieties; and the core layer comprising an olefinic polymer having a melting point greater than the ethylene homopolymer in each of the adhesive layers. Bonding preferably occurs by way of co- extrusion.
- This invention also includes a method of preparing a formed laminar article of manufacture, the method comprising: providing a thermoformable laminar structure that includes at least one pair of two substrate layers and, disposed between the substrate layers, a multiple layer adhesive film as described in the immediately preceding paragraph; and subjecting the laminar structure to conditions of heat and pressure sufficient to convert the structure to the formed laminar article of manufacture.
- the formed article is suitably an automotive panel such as a headiiner.
- FIG. 1 is a schematic representation of a multiple layer adhesive film in accordance with the invention.
- FIG. 2 is a schematic cross-sectional representation of an automotive headiiner in which the multiple layer adhesive film is used to adhere a face fabric to other layers of the headiiner.
- FIG. 3 is a schematic cross-sectional representation of an automotive headiiner in which the multiple layer adhesive films are used for bonding together various layers of the headiiner.
- a multiple layer adhesive film 10 is shown in FIG. 1.
- the multiple layer adhesive film includes a core layer 12, a first outer adhesive layer 13 laminated to a first side of the core layer 12, and a second outer adhesive layer 14 laminated to a second, opposite side of the core layer 12.
- Adhesive layers 13 and 14 are formulated to optimize adhesion at temperatures in excess of 115° centigrade (°C).
- the adhesive layers are also formulated to provide chemical functionality to enhance adhesive characteristics and to bond skin layers (not shown in Fig. 1) to core layer 12.
- the multiple layer adhesive film is particularly well adapted for use in bonding various layers of a thermoformable laminate that is shaped or contoured under application of heat and pressure in a molding tool to form a contoured laminated article such as an automotive headiiner.
- Adhesive layers 13 and 14 are formulated to melt at normal thermoforming processing temperatures (e.g., 1 15°C to 125°C), whereas the core does not melt at such normal thermoforming processing temperatures.
- Core layer 12 serves as a barrier because it has a higher melting point than adhesive layers 13 and 14 and remains solid at such thermoforming temperatures.
- Adhesive layers 13 and 14 comprise a polymer blend including an ethylene homopolymer and an ethylene copolymer.
- the polymers in the polymer blend are preferably selected to have melting points of from 1 15°C to 125°C.
- ethylene homopolymer encompasses homopolymers consisting essentially of ethylene monomer units as well as ethylene polymers containing minor amounts of monomer units other than ethylene provided that such polymers have the characteristics substantially similar to an ethylene homopolymer consisting essentially of ethylene monomer units.
- Suitable ethylene homopolymers include linear low density polyethylene (LLDPE) and low density polyethylene (LDPE).
- Preferred LDPE polymers are prepared using a constrained geometry metallocene catalyst (CGC), such as those disclosed in U.S. Patent No.
- CGC constrained geometry metallocene catalyst
- a commercially available and suitable LLDPE for use in the polymer blend is DOWLEXTM 2247A, which is available from The Dow Chemical Company.
- a preferred LDPE is ELITETM 5110, an enhanced polyethylene resin produced using a CGC (commercially available from The Dow Chemical Company).
- the ethylene copolymer included in the polymer blend of adhesive layers 13 and 14 contains, or has polymerized therein, polar moieties. Such ethylene copolymers are compatible with the ethylene homopolymer.
- the polar moieties of the ethylene copolymer provide a polar functionality that improves adhesion with other materials.
- ethylene copolymers include ethylene/acrylic acid (EAA) copolymer resins and graft-modified ethylene polymers, such as maleic anhydride-modified (MAH- modified) ethylene polymers, especially MAH-modified LLDPE.
- EAA copolymer suitable for EAA ethylene/acrylic acid copolymer resins
- MAH-modified maleic anhydride-modified ethylene polymers
- TM for use in the polymer blend is PRIMACOR 1430 (commercially available from The Dow Chemical Company).
- An anhydride-modified LLDPE that is suitable for use in the polymer ® blend is BYNEL 4104 (commercially available from E. I. duPont de Nemours and
- the polar moiety-containing ethylene copolymer can be used in nearly any amount. However, the amount is preferably from 20 percent to 35 percent by weight (wt percent), based on adhesive layer weight. Amounts below 20 wt percent have a diminished ability to enhance adhesion, and amounts above 35 wt percent generally do not provide sufficient additional benefit to justify the higher cost associated therewith.
- the polymer blend of adhesive layers 13 and 14 preferably contains a minor amount of an anti-blocking concentrate, such as 15 wt percent silicon dioxide (Si ⁇ 2) in 85 wt percent polyethylene (e.g. CN-734 available from Southwest Plastics), the amounts totaling 100 wt percent.
- the polymer blend also preferably contains a minor amount of a processing aid, such as AMPACETTM 10562, which is 3 wt percent VITON® A (a fluoroelastomer available from DuPont Dow Elastomers, L.L.C.) in 97 wt percent polyethylene, the percentages being based on processing aid weight and totaling 100 percent.
- the polymer blend of adhesive layers 13and 14 may also contain other additives such as colorants, UV stabilizers, antioxidants and flame retardants.
- the polymers of core layer 12 preferably have a melting point above 125°C and provide improved strength, improved puncture resistance, improved tear resistance, and improved anti-sag characteristics relative to polymers having a lower melting point.
- Olefinic polymers having a relatively high (greater than 20,000 psi (138 MPa), desirably greater than 25,000 psi (172 MPa), preferably less than or equal to 50,000 psi (345 MPa) although values in excess of 345 MPa may be suitable for some applications) modulus are preferred.
- Examples of preferred olefinic polymers for core layer 12 include propylene homopolymers, propylene copolymers, and high density polyethylene (HDPE).
- Core layer 12 preferably comprises a polymer blend comprises at least one of the above olefinic polymers and a second olefinic polymer that enhances at least one of compatibility and adhesion between the core and the adhesive layers.
- second olefinic polymers include anhydride-modified polyolefins and ultra low density polyethylene (ULDPE).
- the second olefinic polymer is preferably an anhydride-modified polypropylene when the olefinic polymer of the core layer is a propylene homopolymer or a propylene copolymer.
- a suitable commercially available anhydride-modified polypropylene is BYNEL ® 50E571 (E. I. du Pont de Nemours and Company).
- a preferred second olefinic polymer is an ULDPE such as ATTANE® 4201 (commercially available from The Dow Chemical Company).
- the relative amounts of olefinic polymer and second olefinic polymer in the polymer blend of the core layer are not particularly critical. However, the amount of olefinic polymer in core layer 12 is preferably within a range of from 25 percent to 75 percent of the weight of the core layer, and the amount of second olefinic polymer is within a range of from 75 percent to 25 percent of the weight of the core layer.
- the amounts of olefinic polymer and second olefinic polymer are based upon core layer weight and total 100 percent.
- the resulting multiple layer adhesive film has diminished strength properties, diminished puncture resistance, diminished tear resistance, and diminished anti- sag characteristics relative to olefinic polymer amounts within the 25-75 wt percent range.
- the amount of second olefinic polymer is below 25 wt percent, at least one of adhesion and compatibility of core layer 12 with adhesive layers 13 and 14 is diminished relative to second olefinic polymer amounts within the 25-75 wt percent range.
- the total thickness of multiple layer adhesive film 10 is typically from 1 mil (25 micrometers ( ⁇ m)) to 4 mils (100 ⁇ m), and more typically about 2 mils (50 ⁇ m).
- Multiple layer adhesive films 10 are preferably prepared by blown film extrusion. During extrusion, core layer 12 thickness can vary by as much as 15 percent. In order to ensure that core layer 12 has sufficient thickness (despite minor variations in thickness of extruded core layer 12) to achieve the desired strength, puncture resistance, tear resistance, and anti-sag characteristics desired, it preferably comprises from 30 percent to 60 percent of the total thickness of film 10.
- the multiple layer adhesive films of this invention may be either cast or extruded, but are preferably co-extruded. Co-extrusion appears to provide better interiayer contact and bonding than alternate techniques such as casting each layer separately and then forming a multiple layer film.
- the films preferably have a 2 percent secant modulus, as determined by ASTM D882, of at least 25,000 pounds per square inch (psi) (172.4 megapascals (MPa)) at 23°C. In the case of cast film, the modulus is the same in all directions. For extruded films, the modulus is typically greater in the transverse direction than in the machine direction. Thus, for cast films a 2 percent secant modulus of at least
- the multiple layer adhesive films may be used to prepare a variety of articles of manufacture including, without limitation, automotive interior panels.
- the multiple layer adhesive films of this invention may be positioned between substrate layers to form a thermoformable laminate, which may be subsequently molded under application of heat and pressure to form an automotive panel.
- Substrate layers may include, for example, foamed plastics, fabrics, fibrous mats, and random fibers impregnated with thermosetable adhesives.
- FIG. 2 shows a fragmentary cross section of an automotive headiiner 15.
- headiiner 15 comprises a scrim layer 16 that is fabricated from a material such as a non-woven polyester, a layer 17 comprised of random glass fibers impregnated with a polyurethane adhesive, a rigid polyurethane foam layer 18, a layer 19 comprised of random glass fibers impregnated with a polyurethane adhesive, a multiple layer adhesive film 20 (prepared as described above), and a face fabric 21. Face fabric 21 is adhered to layer 19 by film 20.
- the improved strength properties, improved puncture resistance, and improved tear resistance of multiple layer adhesive film 20 allows a laminate comprising layers 15-21 to be more deeply drawn (i.e., highly contoured) during thermoforming without film 20 puncturing or tearing and without allowing uncured urethane adhesive composition in layer 19 to leak or bleed through to face fabric 21.
- film 20 provides a highly effective barrier that prevents damage to face fabric 21 during thermoforming of a laminate comprising layers 16-21 , even when thermoforming includes a high (4 to 5 inches (10.2 to 12.7 centimeters) of draw into a mold) degree of drawing or contouring of the laminate.
- Thermoforming preferably employs a closed mold, a temperature in excess of 300° Fahrenheit (148.9°C) and an applied pressure of from 10 psi (68.9 KPa) up to and including 60 psi (413.7 KPa).
- FIG. 3 illustrates another application of the multiple layer adhesive films of this invention in an automotive headiiner formed from a thermoformable laminate 30.
- Laminate 30 comprises, starting from one side designated as "roof side", a non-woven polyester scrim layer 32, a multiple layer adhesive film layer 33, a layer 34 comprised of random glass fibers (dry), a second multiple layer adhesive film layer 35, a flexible urethane foam layer 36, a third multiple layer adhesive film layer 37, a second dry random glass fiber layer 38, a fourth multiple layer adhesive film layer 39, and a face fabric layer 40.
- thermoformable laminate 30 allows thermoformable laminate 30 to be transformed into a desired shape by application of heat and pressure in a molding tool, and to retain that shape, without using wet or uncured adhesives like a thermosettable urethane adhesive composition.
- the following non-limiting examples illustrate the invention.
- a multiple layer adhesive film comprising a core layer and two adhesive layers, one on each side of the core layer, was prepared by blown film extrusion.
- the inner set point temperature was 390°F (199°C)
- the core set point temperature was 420°F (216°C)
- the outer set point temperature was 410°F (210°C)
- the die temperature was 410°F (210°C)
- the frost line temperature was 229°F (109°C)
- the air ring temperature was 50°F (10°C).
- Each adhesive layer was prepared from a blend that comprised 64 wt percent ELITETM 51 10 polyethylene, 30 wt percent BYNELTM 4104 anhydride-modified LLDPE, and 6 wt percent CN-734 anti-block compound (15 percent Si ⁇ 2 in 85 percent polyethylene), all percentages other than components of the anti-block compound being based on polymer blend weight. Anti-block compound component weights were based on compound weight.
- the polymer blend for the core was 60 wt percent ATTANETM 4201 ULDPE, and 40 wt percent ALATHONTM M6210 HDPE, both percentages being based on polymer blend weight. All polymer pellets were fed to a screw extruder of a blown film coextrusion line.
- the core comprised approximately 60 percent of the thickness of the extruded multiple layer adhesive film, and each of the adhesive layers comprised approximately 20 percent of the thickness of the multiple layer adhesive film.
- the extruded multiple layer adhesive film had a machine direction (extruded direction) modulus of 35,708 psi (246.2 MPa) at room temperature (23°C) and a transverse direction (perpendicular to the machine direction) modulus of 50,235 psi (346.4 MPa).
- DSC Differential scanning calorimetry
- a multiple layer adhesive film was prepared via blown film extrusion using an inner set point temperature of 410°F (210°C), a core set point temperature of 430°F (221 °C), an outer set point temperature of 410°F (210°C), a die temperature of 410°F
- the polymer blends of the adhesive layers were the same as those of Example 1.
- the polymer blend of the core was comprised of 60 weight percent HIMONT HY 6100 polypropylene and 40 wt percent BYNELTM 50E571 anhydride-modified polypropylene.
- the core comprised approximately 50 percent of the total thickness of the multiple layer adhesive film, and each of the adhesive layers comprised approximately 25 percent of the total thickness of the multiple layer adhesive film with the percentages totaling 100 percent).
- the multiple layer adhesive film had a total thickness of 1.94 mils (48.5 ⁇ m).
- the multiple layer adhesive film had a machine direction modulus of 34,504 psi (237.9 MPa) at 23°C and a transverse direction modulus of 60,717 psi (418.6 MPa) at 23°C. DSC was used to determine that the multiple layer adhesive film had melting points at 123°C and at 156°C.
- a multiple layer adhesive film was prepared via blown film extrusion using the temperatures specified in Example 2.
- the polymer blend for each of the adhesive layers comprised 53 weight percent DOWLEX ® 2247 A LLDPE, 40 wt percent PRIMACOR ® 1430 EAA copolymer resin, 6 wt percent of its anti-blocking concentrate of Example 1 , and
- the polymer blend of the core comprised 70 wt percent INSPIRE ® C103-04 polypropylene copolymer and 30 wt percent of the anhydride-modified polypropylene of Example 2.
- the core layer comprised approximately 40 percent of the total thickness of the multiple layer adhesive film, and each of the adhesive layers comprised approximately 30 percent of the total thickness of the multiple layer adhesive film with the percentages totaling 100 percent.
- the composition of each layer also totaled 100 percent.
- the multiple layer adhesive film had a total thickness of 2.25 mils (56.25 ⁇ m).
- the multiple layer adhesive film had a machine direction 2 percent secant modulus of 57,500 psi (396.4 MPa) at room temperature (23°C) and a transverse direction
- a multiple layer adhesive film was prepared via cast film extrusion.
- the polymer blend for each of two adhesive layers comprised 54 wt percent of the same LLDPE as in Example 3, 40 wt percent of the same EAA as in Example 3 copolymer resin, 5 wt CN-744 antiblocking concentrate (20 percent Si ⁇ 2 in 80 percent polyethylene, available from Southwest Plastics), and 1 wt percent of the same process aid as in Example 3.
- the polymer blend of the core was the same as in Example 3.
- the core layer comprised approximately 30 percent of the total thickness of the multiple layer adhesive film, and each of the adhesive layers comprised approximately 35 percent of the total thickness of the multiple layer adhesive film with the percentages totaling 100 percent.
- the multiple layer adhesive film had a total of 1.98 mils (1.98 ⁇ m).
- the multiple layer adhesive film had a machine direction 1 percent secant modulus of 40,750 psi (281.0 MPa) at room temperature (23°C) and a transverse direction
- thermoplastic adhesive films Three automotive headliners utilizing thermoplastic adhesive films were prepared.
- the automotive headliners were identical except for the adhesive film used.
- the first headiiner, used as a control, was prepared utilizing a commercially available multipurpose monolayer adhesive film (INTEGRALTM 909 from The Dow Chemical Company) which is commonly employed in automotive headliners.
- the multiple layer adhesive films of Examples 1 and 3 were used respectively in the second and third automotive headliners.
- a sag test was performed on each of the headliners. The sag test involved placing the headiiner in a simulated roof bucket and subjecting it to a series of environmental conditions, including exposure to high (typically 1 10-120°C) temperatures which may be encountered in a closed vehicle on a sunny day.
- each headiiner was measured for sag at the edges, and the second headiiner (the one utilizing the adhesive film from Example 1 ) was tested for sag at the center.
- the testing was in conformance with a Ford Motor Company specification that requires a maximum of 13 millimeters (mm) of sag at the center of the headiiner and a maximum of 3.5 millimeters of sag at the edge of the headiiner.
- mm millimeters
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- Chemical Kinetics & Catalysis (AREA)
- Laminated Bodies (AREA)
Abstract
L'invention concerne un film adhésif à couches multiples possédant des caractéristiques à haute température, des propriétés barrière, et une résistance au percement et au déchirement. Ce film adhésif comprend au moins trois couches dont une couche centrale collée par liaison ou stratification à deux couches adhésives externes. Chaque couche adhésive est formée à partir d'un mélange de polymères contenant au moins un homopolymère éthylique et un copolymère éthylique ayant des fractions polaires. La couche centrale contient un polymère oléfinique dont le point de fusion est supérieur à celui de n'importe quel autre polymère de couche adhésive. Plusieurs films adhésifs à couches multiples peuvent être utilisés dans une structure stratifiée thermoformable incluant des couches fabriquées à partir de matériaux polymériques ou non polymériques.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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AU45522/99A AU4552299A (en) | 1998-06-10 | 1999-06-08 | Multilayer adhesive film |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US8880298P | 1998-06-10 | 1998-06-10 | |
US60/088,802 | 1998-06-10 |
Publications (1)
Publication Number | Publication Date |
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WO1999064533A1 true WO1999064533A1 (fr) | 1999-12-16 |
Family
ID=22213573
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1999/012789 WO1999064533A1 (fr) | 1998-06-10 | 1999-06-08 | Films adhesifs a couches multiples |
Country Status (2)
Country | Link |
---|---|
AU (1) | AU4552299A (fr) |
WO (1) | WO1999064533A1 (fr) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006119588A1 (fr) * | 2005-05-11 | 2006-11-16 | Mondi Belcoat, Naamloze Vennootschap | Structure stratifiee amelioree et son procede de fabrication |
EP1772258A1 (fr) * | 2005-10-06 | 2007-04-11 | J. H. Ziegler GmbH & Co. KG | Stratifié non-tissé infiltrable par une composition thermoplastique pour la préparation de pièces renforcées |
WO2007095667A1 (fr) * | 2006-02-20 | 2007-08-30 | Huhtamaki New Zealand Limited | Emballage ameliore pour produits |
WO2008005110A1 (fr) * | 2006-06-29 | 2008-01-10 | Dow Global Technologies Inc. | Films adhésifs de protection |
WO2020065560A1 (fr) * | 2018-09-25 | 2020-04-02 | Proprietect L.P. | Article en mousse composite |
WO2020065564A1 (fr) * | 2018-09-25 | 2020-04-02 | Proprietect L.P. | Article en mousse composite |
US20230069869A1 (en) * | 2021-09-03 | 2023-03-09 | Graham Williams | Self-reinforced polymer structures |
IT202200013846A1 (it) * | 2022-06-30 | 2023-12-30 | Ind Termoplastica Pavese S P A | Film polimerico per la copertura di autoveicoli |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3330185A1 (de) * | 1982-01-18 | 1984-02-23 | Chemplex Co., 60008 Rolling Meadows, Ill. | Verbundwerkstoffe und deren herstellung |
EP0713765A2 (fr) * | 1994-11-24 | 1996-05-29 | Wolff Walsrode Ag | Feuille multicouche scellable, sans adhésif, ayant aptitude à l'emboutissage profond et stérilisable |
-
1999
- 1999-06-08 WO PCT/US1999/012789 patent/WO1999064533A1/fr active Application Filing
- 1999-06-08 AU AU45522/99A patent/AU4552299A/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3330185A1 (de) * | 1982-01-18 | 1984-02-23 | Chemplex Co., 60008 Rolling Meadows, Ill. | Verbundwerkstoffe und deren herstellung |
EP0713765A2 (fr) * | 1994-11-24 | 1996-05-29 | Wolff Walsrode Ag | Feuille multicouche scellable, sans adhésif, ayant aptitude à l'emboutissage profond et stérilisable |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006119588A1 (fr) * | 2005-05-11 | 2006-11-16 | Mondi Belcoat, Naamloze Vennootschap | Structure stratifiee amelioree et son procede de fabrication |
EP1772258A1 (fr) * | 2005-10-06 | 2007-04-11 | J. H. Ziegler GmbH & Co. KG | Stratifié non-tissé infiltrable par une composition thermoplastique pour la préparation de pièces renforcées |
WO2007095667A1 (fr) * | 2006-02-20 | 2007-08-30 | Huhtamaki New Zealand Limited | Emballage ameliore pour produits |
WO2008005110A1 (fr) * | 2006-06-29 | 2008-01-10 | Dow Global Technologies Inc. | Films adhésifs de protection |
US7939169B2 (en) | 2006-06-29 | 2011-05-10 | Dow Global Technologies Llc | Thermoplastic olefin polymer blend and adhesive films made therefrom |
AU2007270031B2 (en) * | 2006-06-29 | 2012-10-25 | Dow Global Technologies Llc | Protective adhesive films |
WO2020065560A1 (fr) * | 2018-09-25 | 2020-04-02 | Proprietect L.P. | Article en mousse composite |
WO2020065564A1 (fr) * | 2018-09-25 | 2020-04-02 | Proprietect L.P. | Article en mousse composite |
US11926137B2 (en) | 2018-09-25 | 2024-03-12 | Proprietect L.P. | Composite foam article |
US12011912B2 (en) | 2018-09-25 | 2024-06-18 | Proprietect L.P. | Composite foam article |
US20230069869A1 (en) * | 2021-09-03 | 2023-03-09 | Graham Williams | Self-reinforced polymer structures |
IT202200013846A1 (it) * | 2022-06-30 | 2023-12-30 | Ind Termoplastica Pavese S P A | Film polimerico per la copertura di autoveicoli |
EP4306291A1 (fr) * | 2022-06-30 | 2024-01-17 | Industria Termoplastica Pavese S.p.A. | Film polymère pour couvrir des voitures |
Also Published As
Publication number | Publication date |
---|---|
AU4552299A (en) | 1999-12-30 |
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