Classifications

• • 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
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B1/00—Layered products having a non-planar shape
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B1/00—Layered products having a non-planar shape
  • B32B1/08—Tubular products
• • 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
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  • 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
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
  • B32B27/281—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyimides
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
  • B32B27/285—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyethers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
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  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
  • B32B27/286—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polysulphones; polysulfides
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • 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
  • B32B27/302—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising aromatic vinyl (co)polymers, e.g. styrenic (co)polymers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
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  • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
  • B32B27/304—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl halide (co)polymers, e.g. PVC, PVDC, PVF, PVDF
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
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  • 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
  • B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
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  • 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
  • B32B27/308—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising acrylic (co)polymers
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B27/00—Layered products comprising a layer of synthetic resin
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
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  • B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
  • B32B3/02—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions
  • B32B3/04—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions characterised by at least one layer folded at the edge, e.g. over another layer ; characterised by at least one layer enveloping or enclosing a material
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • 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
• • E—FIXED CONSTRUCTIONS
  • E04—BUILDING
  • E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
  • E04B1/00—Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
  • E04B1/38—Connections for building structures in general
  • E04B1/541—Joints substantially without separate connecting elements, e.g. jointing by inter-engagement
• • E—FIXED CONSTRUCTIONS
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  • E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
  • E04B1/00—Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
  • E04B1/62—Insulation or other protection; Elements or use of specified material therefor
  • E04B1/66—Sealings
  • E04B1/665—Sheets or foils impervious to water and water vapor
• • E—FIXED CONSTRUCTIONS
  • E04—BUILDING
  • E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
  • E04B7/00—Roofs; Roof construction with regard to insulation
  • E04B7/18—Special structures in or on roofs, e.g. dormer windows
• • E—FIXED CONSTRUCTIONS
  • E04—BUILDING
  • E04C—STRUCTURAL ELEMENTS; BUILDING MATERIALS
  • E04C2/00—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
  • E04C2/02—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials
  • E04C2/10—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of wood, fibres, chips, vegetable stems, or the like; of plastics; of foamed products
  • E04C2/20—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of wood, fibres, chips, vegetable stems, or the like; of plastics; of foamed products of plastics
• • E—FIXED CONSTRUCTIONS
  • E04—BUILDING
  • E04C—STRUCTURAL ELEMENTS; BUILDING MATERIALS
  • E04C2/00—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
  • E04C2/54—Slab-like translucent elements
• • E—FIXED CONSTRUCTIONS
  • E04—BUILDING
  • E04D—ROOF COVERINGS; SKY-LIGHTS; GUTTERS; ROOF-WORKING TOOLS
  • E04D5/00—Roof covering by making use of flexible material, e.g. supplied in roll form
• • H—ELECTRICITY
  • H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
  • H02S—GENERATION OF ELECTRIC POWER BY CONVERSION OF INFRARED RADIATION, VISIBLE LIGHT OR ULTRAVIOLET LIGHT, e.g. USING PHOTOVOLTAIC [PV] MODULES
  • H02S20/00—Supporting structures for PV modules
  • H02S20/20—Supporting structures directly fixed to an immovable object
  • H02S20/22—Supporting structures directly fixed to an immovable object specially adapted for buildings
  • H02S20/26—Building materials integrated with PV modules, e.g. façade elements
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B2250/00—Layers arrangement
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B2250/00—Layers arrangement
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B2255/00—Coating on the layer surface
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B32B2307/306—Resistant to heat
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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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
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
  • Y02B10/00—Integration of renewable energy sources in buildings
  • Y02B10/10—Photovoltaic [PV]
• • 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
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
  • Y02E10/00—Energy generation through renewable energy sources
  • Y02E10/50—Photovoltaic [PV] energy

Definitions

• the present disclosure relates generally to multilayer polymer films. Specifically, the present disclosure relates to multilayer composite films for architectural applications.
• Ethylene tetrafluoroethylene can be used in some architectural applications in place of conventional architectural glasses or plastics (e.g., tempered silicate glass, glass ceramics, polycarbonate). This is due, in part, to the light weight, visible light transparency and translucency, thermal stability, and flexibility exhibited by ETFE sheets.
• ETFE is often either configured in a single layer that is supported by a network of cables or as a series of pneumatic cushions formed by joining of between two and five layers of ETFE together and inflating a space defined by the joined ETFE layers (and also sometimes supported by a network of cables).
• ETFE is extruded as a single sheet or a multilayer sheet. ETFE sheets are joined together to form an envelope, which is then assembled into an architectural panel by attaching the envelope to a frame made from a structural material (e.g., aluminum, steel). The frame and the attached envelopes are in turn joined to supports of an architectural structure. The ETFE envelopes are inflated to form the pneumatic cushion.
• Pressure is maintained within the ETFE pneumatic cushions using a pressurization unit (such as a compressor) that maintains an internal pressure of the ETFE pneumatic cushions at approximately 220 Pa, thus providing structural stability to the pneumatic pillow.
• a pressurization unit such as a compressor
• An example of the present disclosure includes a multilayer composite film including: an outer ethylene tetrafluoroethylene (ETFE) layer having a first major surface and a second major surface, the first major surface configured as an exterior surface of the multilayer composite film and the second major surface opposite the first major surface; a structural polymer layer proximate to the second major surface of the outer ETFE layer; a first ETFE layer having a first major surface and a second major surface, the first major surface configured as an exterior surface of the multilayer composite film and the second major surface opposite the first major surface; a structural polymer layer proximate to the second major surface of the outer ETFE layer; a first
• ETFE ethylene tetrafluoroethylene
• fluoropolymer adhesive layer disposed between the second major surface of the outer ETFE layer and the structural polymer layer, the first fluoropolymer adhesive layer adhering the outer ETFE layer and the structural polymer layer together; a second ETFE layer having a first major surface and a second major surface, the first major surface of the second ETFE layer proximate to the structural polymer layer and the second major surface of the second ETFE layer configured as an interior surface opposite the first major surface of the outer ETFE layer; and a second fluoropolymer adhesive disposed between the first major surface of the second ETFE layer and the structural polymer layer, the second fluoropolymer adhesive layer adhering the second ETFE layer and the structural polymer layer together.
• the multilayer composite film further includes a fire retardant rating of V0 when tested according to a UL94 standard.
• the multilayer composite film further includes an infra-red (IR) radiation rejection layer disposed in or on at least one of the structural polymer layer, the first fluoropolymer adhesive layer, the second fluoropolymer adhesive layer, and the outer ETFE layer, the IR radiation rejection layer configured to reflect at least 40% of incident IR radiation.
• IR infra-red
• the IR radiation rejection layer includes a metal layer disposed on one of the structural polymer layer and the ETFE layer, the metal layer having a reflectance of greater than 40% for wavelengths of radiation between 700 nm and 1000 nm and having a transmittance of visible light having wavelengths between 400 nm and 700 nm greater than 50%.
• the metal layer is one of a copper film, a silver film, a gold film, a nickel film, a metal oxide film, an aluminum film, and combinations thereof.
• the metal layer has a thickness between 1 nm and 500 nm.
• the IR radiation rejection layer includes at least one of titanium dioxide nanoparticles, silver particles, gold particles, and aluminum nanoparticles disposed in at least one of the first fluoropolymer adhesive layer and the second fluoropolymer adhesive layer.
• the multilayer composite film has a young's modulus of at least 1000 MPa and an ultimate tensile strength of at least 146 MPa.
• the multilayer composite film exhibits a yield point under tensile strain of at least 40 MPa.
• the outer ETFE layer has a thickness of between 25 microns and 125 microns.
• the second ETFE layer has a thickness from 25 microns to 125 microns.
• the multilayer composite film where structural polymer layer is a polyethylene terephthalate (PET) layer.
• PET polyethylene terephthalate
• multilayer composite film where the structural polymer layer has a thickness from 50 microns to 250 microns.
• the multilayer composite film where at least one of the first fluoropolymer adhesive layer and the second fluoropolymer adhesive layer includes a fluoropolymer resin, an ultra-violet light absorbent component, and a crosslinking component.
• the multilayer composite film where the fluoropolymer resin is at least 40 weight % of at least one of the first fluoropolymer layer and the second fluoropolymer layer. In an embodiment of the multilayer composite film, wherein the multilayer composite film where the fluoropolymer resin consists essentially of fluoropolymer-based polymers. In an embodiment of the multilayer composite film, wherein the multilayer composite film where at least one of the first fluoropolymer adhesive layer and the second fluoropolymer adhesive layer has a thickness from 5 microns to 30 microns.
• the multilayer composite film further includes a perimeter edge configured to form a cord edge, where the second major surface of the second ETFE layer is adhered to itself using at least one of an adhesive and an adhesive tape.
• the multilayer composite film further including a rigid structure disposed within a volume defined by the cord edge.
• the multilayer composite film has a haze value of less than 16%.
• the multilayer composite film has a haze value of from 2% to 14%.
• An example of the present disclosure includes a multilayer composite film including: an outer fluorinated polymer layer having a first major surface and a second major surface, the first major surface configured as an exterior surface of the multilayer composite film and the second major surface opposite the first major surface; a non-fluorinated polymer layer proximate to the second major surface of the outer fluorinated polymer layer; a first fluoropolymer adhesive layer disposed between the second major surface of the outer fluorinated polymer layer and the non-fluorinated polymer layer, the first fluoropolymer adhesive layer adhering the outer fluorinated polymer layer and the non-fluorinated polymer layer together; and a portion of the multilayer composite film defining an integral tube, the integral tube including a perimeter edge of the multilayer composite film curled back onto the multilayer composite film and permanently adhered to the multilayer composite film.
• the integral tube forms a cord edge.
• the multilayer composite film further includes a first sheet of the multilayer composite film joined to a second sheet of the multilayer composite film.
• the first sheet is joined to the second sheet using at least one of a lapp joint, a lapp joint and a strip, and a butt joint.
• the first sheet is joined to the second sheet by at least one of an adhesive tape, an adhesive, and a heat seal.
• the non-fluorinated polymer layer comprises PET.
• the multilayer composite film further including an IR reflecting layer or IR absorbing agent.
• the outer fluorinated polymer layer is an ETFE layer.
• the outer fluorinated polymer layer is a polyvinyl fluoride layer.
• the outer fluorinated polymer layer is an ethylene chlorotrifluoroethylene layer.
• the outer fluorinated polymer layer is a polyvinylidene fluoride layer.
• the outer fluorinated polymer layer is a polychlorotrifluoroethylene layer.
• the outer fluorinated polymer layer is a polyfluoroethylenepropropylene layer.
• FIG. 1 A is a cross-sectional view of an ETFE-containing multilayer composite film comprising a single ETFE layer, in an embodiment.
• FIG. 1 A' is a cross-sectional view of an ETFE-containing multilayer composite film comprising a single ETFE layer, in an embodiment.
• FIG. IB is a cross-sectional view of an ETFE-containing multilayer composite film that includes particles that can reflect and/or absorb IR radiation, in an embodiment.
• FIG. 2. is a cross-sectional view of an ETFE-containing multilayer composite film comprising two layers of ETFE, in an embodiment.
• FIG. 3 is a graph of stress-strain data for both of an ETFE-containing multilayer composite film and a film comprising an ETFE bilayer.
• FIG. 4 is a graph of reflectance data for an ETFE-containing multilayer composite film, in an embodiment.
• FIGS. 5A-5C illustrate various joint configurations for joining multilayer composite films together, in embodiments.
• FIG. 6 is a cross-sectional view of an ETFE-containing multilayer composite film configured for use as a structural panel, in another embodiment.
• FIG. 7 A is a cross-sectional view of an ETFE-containing multilayer composite film configured for use as a structural panel, in an embodiment.
• FIG. 7B is a cross-sectional view of an ETFE-containing multilayer composite film configured for attachment to a support cable, in an embodiment.
• ETFE films have drawbacks that limit their applicability to architectural applications.
• ETFE films have mechanical properties that do not generally lend themselves to use for structural elements of architectural applications.
• ETFE films generally have a low Young's modulus (about 800 MPa to about 1500 MPa) and have a relatively low yield point, after which the ETFE films deform elastically.
• ETFE films are usually applied to architectural applications by configuring the ETFE film as a pneumatic cushion, as described above.
• An alternative embodiment uses single-ply ETFE panels that are supported by a network or grid of support cables that are separated by about one meter (m). Fabricating pneumatic cushions and maintaining pressure within the pneumatic cushions adds expense to the maintenance of the individual structural elements and the architectural application as a whole. Similarly, fabricating and maintaining a network of support cables adds expense to the use of ETFE as an architectural element and also detracts from the aesthetic appeal of the otherwise transparent ETFE architectural elements.
• embodiments of the present disclosure include a multilayer composite film that includes an outer ETFE layer adhered to a structural polymer film, such as polyethylene terephthalate (PET), among others, by an adhesive.
• the multilayer composite film may also include an infra-red (IR) radiation rejection layer that reflects at least 40% of incident IR radiation (light having a wavelength from 700 nm to 1000 nm), thus reducing the amount of IR radiation transmitted into an area defined, at least in part, by the optically transparent multilayer composite film.
• IR infra-red
• Another advantage of using embodiments described herein as an architectural element is that the improved rigidity (from the flexural modulus of the structural polymer being higher than that of ETFE) and strength can increase the spacing (e.g., from the current 1 m spacing to at least 15 m) between support cables of a corresponding network, thus improving the visual appeal of ETFE architectural elements.
• Yet another advantage of embodiments described herein is reduction in the haze in architectural elements using a multilayer composite film of the present disclosure compared to architectural components that currently use only ETFE.
• Current ETFE architectural components are about 250 ⁇ thick. This thickness of ETFE has a visibly hazy appearance (measured according to ASTM D1003-13).
• Embodiments disclosed herein have a haze value of less than 20%, less than 16%, less than 12%, less than 10%, less than 8% and in some cases between 2% and 14%) and in other cases about 6%> (as measured according to ASTM D 1003- 13 using a BYK Gardner Haze Guard Plus haze meter).
• Embodiments described herein can include one or more layers of ETFE, each of which is as thin as 25 ⁇ .
• a structural polymer layer used as a component of the multilayer composite film can be selected to have greater clarity (i.e., lower haze) than ETFE, thus further improving the visual clarity and aesthetic appearance of the architectural components using an embodiment of the multilayer composite film compared to single ply ETFE architectural components currently used.
• FIG. 1A is a cross-sectional view of an example multilayer composite film 100, in an embodiment.
• the multilayer composite film 100 includes an ETFE layer 104, a structural polymer layer 108, an adhesive 1 12, and an optional IR radiation rejection layer 1 16.
• the multilayer composite film 100 has a thickness, indicated by a in FIG. 1 A, that can be within any of the following ranges: 50 to 1000 ⁇ , 100 to 1000 ⁇ , 200 to 1000 ⁇ , 200 to 800 ⁇ , 200 to 600 ⁇ , greater than 100 ⁇ , greater than 200 ⁇ , greater than 500 ⁇ , less than 3 mm, less than 2 mm, less than 1 mm, less than 800 ⁇ , less than 500 ⁇ , less than 400 ⁇ or less than 300 ⁇ .
• the outer ETFE layer 104 of the multilayer composite film 100 is shown in this example as including a single sheet of ETFE material. In other examples, not shown, the ETFE layer 104 can include multiple ETFE sheets to form the outer ETFE layer 104. Other
• the outer ETFE layer 104 has a thickness, indicated by ⁇ in FIG. 1 A, that can be, for example, within any of the following ranges: 25 microns ( ⁇ ) to 250 ⁇ ; 25 ⁇ to 100 ⁇ ; 25 ⁇ to 75 ⁇ ; 25 ⁇ to 50 ⁇ ; 50 ⁇ to 150 ⁇ ; 50 ⁇ to 100 ⁇ ; 75 ⁇ to 200 ⁇ ; 75 ⁇ to 100 ⁇ ; 100 ⁇ to 200 ⁇ .
• the outer ETFE layer 104 is also shown as including a first major surface and a second major surface. These will be used for convenience to describe the structure and fabrication of the multilayer composite film 100 in more detail below.
• the outer ETFE layer 104 is configured to be disposed as an exterior-facing surface of the multilayer composite film 100. More specifically, for convenience of explanation, the first major surface of the outer ETFE layer 104 can be used to form an exterior surface (i.e., exposed to the earth's atmosphere) of an architectural application. Placing the outer ETFE layer 104 at an exterior surface employs many of the beneficial properties of ETFE material that may otherwise be lacking in more conventional architectural materials. For example, the low surface energy of ETFE helps shed water and resist accumulation of atmospherically born contaminants (e.g., soot, dirt, dust, pollen).
• atmospherically born contaminants e.g., soot, dirt, dust, pollen
• ETFE and more generally fluorinated polymers, can also exhibit resistance to solvation or other chemical degradation caused by atmospherically borne contaminants and chemicals intentionally applied (e.g., cleaners, detergents) and unintentionally applied (e.g., a spill) to an exterior surface of an architectural application.
• This low surface energy improves the longevity of the multilayer composite film 100 because the film can resist chemically induced degradation.
• ETFE transmits as much as 90% or 95% of the intensity of incident visible light (e.g., radiation between wavelengths of 400 nanometers (nm) and 700 nm). This high transmissivity of ETFE is appealing in many architectural applications in which natural light is desired.
• fluorinated polymers may be substituted for the outer ETFE layer 104, as well as other ETFE layers identified in other embodiments described below.
• Alternative fluorinated polymers include, but are not limited to, ethylene chlorotrifluoroethylene (ECTFE), polyvinyl fluoride (PVF), polyvinylidene fluoride (PVDF),
• PCTFE polychlorotrifluoroethylene
• FEP polyfluoroethylenepropropylene
• PFA perfluoroalkyl-tetrafluoroethylene
• Lumiflon® a copolymer of chlorotrifluoroethylene and modified hydroxyl-functionalized vinyl ethers and available from Asahi Glass Company, Ltd. of Tokyo, Japan
• Zeffle ® a copolymer of tetrafluoroethylene and modified hydroxyl- functionalized vinyl esters and available from ® (available from Daikin Industries, Ltd. of Osaka, Japan)
• fluorinated polymethacrylates fluorinated epoxy films
• CTFE/VDF perfluoroalkyl-tetrafluoroethylene
• TFE/FIFP tetrafluoroethylene- hexafluoropropylene copolymer
• FIFP/VDF hexafluoropropylene-vinylidene fluoride
• TFE- PFMe tetrafluoroethylene-perfluoromethylether copolymer
• the multilayer composite film 100 includes at least one structural polymer layer 108, as shown in FIG. 1 A.
• the structural polymer layer 108 of the multilayer composite film 100 adds structural integrity (e.g., higher Young's modulus, flexural modulus, ultimate tensile strength) to the multilayer composite film 100 without compromising the benefits of the outer ETFE layer 104 described above.
• structural integrity e.g., higher Young's modulus, flexural modulus, ultimate tensile strength
• PET polyethylene terephthalate
• ETFE can have a Young's modulus of approximately 800 MPa (mega pascals) to 1500 MPa, a flexural modulus of approximately 1.2 GPa (giga pascals), and an ultimate tensile strength of approximately 46 MPa (within normal measurement variation and natural variation between samples).
• PET can exhibit a Young's modulus of approximately 2000 MPa to approximately 4000 MPa, a flexural modulus of approximately 8.3 GPa to approximately 14 GPa, and an ultimate tensile strength of approximately 60 MPa to approximately 140 MPa (within normal measurement variation and natural variation between samples).
• the polymer selected for use as the structural polymer layer 108 does not substantially decrease the transparency, translucence or clarity of the outer ETFE layer 104 while at the same time improving the structural properties of the multilayer composite film, as explained above.
• the structural polymer layer 108 can exhibit visible light transmission of greater than 40%, greater than 75%, greater than 85%, greater than 90%) or greater than 95% at thicknesses of 25 ⁇ , 50 ⁇ , 100 ⁇ , 150 ⁇ , 200 ⁇ , 300 ⁇ , and 400 ⁇ .
• the haze of the multilayer composite films of the present disclosure can be as low as from 2% to 16% (in some cases about 6%)) and have visible light transmittances of as high (or higher) as 40%, 75%, 85%, 90%, or 95%). These improvements are present even for multilayer composite films having a comparable thickness to ETFE architectural films currently used (often as thick as 250 mm) because the structural polymer layer 108 can be selected to have an equivalent or higher visible light transmittance than ETFE (or other fluoropolymers used in place of ETFE).
• the structural polymer layer 108 has improved mechanical properties over ETFE (and other fluoropolymers), the overall thickness of some embodiments of multilayer composite films can be reduced compared to ETFE architectural films currently used, thus further increasing the relative clarity and light transmittance of multilayer composite films described herein.
• the structural polymer layer 108 can have a thickness, indicated by ⁇ in FIG. 1 A, that can be, for example, within any of the following ranges: 25 microns (um) to 250 ⁇ ; 25 ⁇ to 100 ⁇ ; 25 ⁇ to 75 ⁇ ; 25 ⁇ to 50 ⁇ ; 50 ⁇ to 150 ⁇ ; 50 ⁇ to 100 ⁇ ; 75 ⁇ to 200 ⁇ ; 75 ⁇ to 100 ⁇ ; 100 ⁇ to 200 ⁇ ; greater than 50 rn, greater than 100 rn, greater than 150 m, less than 2 mm, less than 1 mm, less than 800 m, less than 500 m, less than 300 ⁇ or less than 200 m.
• the thickness of the structural polymer layer 108 is selected based on the various material properties (e.g., Young's modulus, flexural modulus, ultimate tensile strength, among others).
• Polymers other than PET can be used for the structural polymer 108.
• Alternatives to PET include polymer films that have beneficial mechanical properties and high transmissivities to visible light.
• the structural polymer layer 108 can exhibit a Young's modulus of greater than 500 MPa, greater than 1000 MPa or greater than 4000 MPa and visible light transmission of greater than 40%, greater than 90%, greater than 95% or greater than 99% for a film having a thickness of 100 m.
• the polymers can be extruded films or free-standing films that may include, but are not limited to: polypropylene, polyethylene, polyethylene vinyl acetate, polycarbonates, cellulose and cellulose derivatives, polyamide-imide, polyurethanes,
• polyacrylates polymethacrylates, polythiophenes, poly(3,4-ethylenedioxythio-phene)/polystyrene sulfonate, polystyrene, biopolymers, fluoropolymers, chlorofluoropolymers, vinylfluoropolymers, poly (vinyl chloride), polyethers, polyimides, polyetherimides, polyphenylsulfone, and combinations thereof.
• the adhesive 112 of the multilayer composite film 100 is used to join the structural polymer layer 108 to the second major surface of the outer ETFE layer 104, as shown in FIG. 1 A.
• the adhesive can be a fluoropolymer adhesive 112 that has high thermal stability, hydrolysis resistance, and UV stability. These properties facilitate long term adhesion between the structural polymer layer 108 and the outer ETFE layer 104 even when subjected to months and years of solar-induced heating and solar irradiation, respectively.
• the strength of adhesion between the structural polymer layer 108 and the outer ETFE layer 104 provided by the fluoropolymer adhesive 112 can, in some embodiments, be within any of the following ranges: from 1 Newton(N)/centimeter (cm) to 10 N/cm; from 1 N/cm to 5 N/cm; from 1 N/cm to 3 N/cm; from 2 N/cm to 10 N/cm; from 2 N/cm to 7 N/cm; from 3 N/cm to 7 N/cm; from 5 N/cm to 10 N/cm; from 5 N/cm to 10 N/cm; greater than 3 N/cm, greater than 5 N/cm or greater than 7 N/cm.
• the fluoropolymer adhesive 112 has a thickness, indicated by ⁇ in FIG. 1 A, that can be within any of the following ranges: 2 ⁇ to 50 ⁇ ; 2 ⁇ to 30 ⁇ ; 5 ⁇ to 30 ⁇ ; 10 ⁇ to 30 ⁇ ; 15 ⁇ to 30 ⁇ .
• fluoropolymer resins used as a component of the fluoropolymer adhesive 112 include fluoro-copolymer resins and fluoropolymer resins that are terpolymers.
• fluoropolymer resins used as a component of the fluoropolymer adhesive 112 include, but are not limited to, perfluoroalkyl vinyl ethers such as Lumiflon® (available from Asahi Glass Company, Ltd. of Tokyo, Japan) and tetrafluoroethylene based copolymers, such as Zeffle® (available from Daikin Industries, Ltd. of Osaka, Japan).
• the fluoropolymer adhesive 112 may be free of adhesives other than
• fluoropolymers e.g., free of acrylic, polyol and other adhesives.
• the fluoropolymer adhesive 112 includes one or more non- fluorinated components in addition to the fluorinated resin component.
• the fluoropolymer adhesive 112 includes an amine or hydroxyl polyol fluorinated resin.
• the fluoropolymer adhesive 112 may include a polyester polyol adhesive component, such as Adcote 76R40 (available from Rohm and Haas of Philadelphia, Pennsylvania, United States).
• fluoropolymer adhesive 112 composition include a UV absorber that improves the stability of the fluoropolymer adhesive 112 and underlying layers upon exposure to light include nitroxy radical based compounds, among others.
• UV absorbers that can be added to the fluoropolymer adhesive 112 include Uvinul 3050, Tinuvin® 400, Tinuvin® 477, Tinuvin® 479, Tinuvin® 384-2, Tinuvin® 1600 , Tinuvin® P, Tinuvin® CarboProtect, Tinuvin® 5000 series (all of which are available from BASF of Ludwigshafen, Germany), Evesorb 74 (from Everlight Chemical of Taipei, Taiwan), and inorganic UV absorbers such as zinc oxide, cerium oxide, titanium dioxide, and transparent iron oxides.
• the fluoropolymer adhesive 112 composition may also include a hindered amine light stabilizer (HALS) to further improve resistance to UV light degradation and improve the performance of an included UV light absorber.
• HALS hindered amine light stabilizer
• HALS include but are not limited to Tinuvin® 123, Tinuvin® 171 (which are available from BASF), and combinations thereof.
• Flame retardants which may also be included as a component in the fluoropolymer adhesive 112 composition include non-halogenated flame retardants such as Exolit® OP550, Exolit® OP560 (both of which are available from Clariant Manufacturing Company of Muttenz, Switzerland), Levagard®4090N (available from Rhein Chemie of Mannheim, Germany), or mixtures thereof.
• Organic solvents that may be used for the synthesis of the fluoropolymer adhesive 112 include but are not limited to organic solvents such as methyl ethyl ketone (MEK), acetone, methyl isobutyl ketone (MIBK), toluene, xylene, methanol, heptane, ethyl acetate, isopropyl acetate, n-butyl acetate, or mixtures thereof.
• MEK methyl ethyl ketone
• MIBK methyl isobutyl ketone
• toluene xylene
• methanol heptane
• ethyl acetate isopropyl acetate
• n-butyl acetate or mixtures thereof.
• the adhesive compositions of various embodiments can be applied to polymeric film by any of a variety of methods known to those skilled in the art of film coating manufacture. Suitable application methods include application by Meyer rod coating, com
• the fluoropolymer adhesive 112 can be prepared by mixing a fluoropolymer resin and a crosslinking agent in an organic solvent.
• Other components such as ultra-violet (UV) radiation absorbing compounds, IR reflective and/or absorbing compounds, among others, can also be added to the organic solvent.
• UV radiation absorbing compounds such as ultra-violet (UV) radiation absorbing compounds, IR reflective and/or absorbing compounds, among others, can also be added to the organic solvent.
• UV radiation absorbing compounds such as ultra-violet (UV) radiation absorbing compounds, IR reflective and/or absorbing compounds, among others
• UV radiation absorbing compounds such as ultra-violet (UV) radiation absorbing compounds, IR reflective and/or absorbing compounds, among others
• UV radiation absorbing compounds such as ultra-violet (UV) radiation absorbing compounds, IR reflective and/or absorbing compounds, among others
• the following mixture can be assembled: 50 parts to 200 parts by weight of fluoropolymer resin; 2 parts to 20 parts by
• the now crosslinked adhesive composition may comprise at least 20%, at least 30% at least 40%, at least 50%), at least 60%>, at least 70%, at least 80%>, or at least 90% fluoropolymer by weight.
• An example formulation of fluoropolymer adhesive 112 follows in Table 1.
• Tinuvin® 384-2 (BASF) UV absorber 4.4
• Optional IR radiation rejection layer 116 of the multilayer composite film 100 may actually include one or both of IR reflecting materials and IR absorbing materials.
• the IR radiation rejection layer 116 reduces the amount of IR radiation passing through the multilayer composite film 100, thus reducing the IR-induced heating of the interior spaces within an architectural structure.
• IR absorbing materials absorb infrared radiation in the film composite and prevent much of the incident IR radiation from reaching the interior of the structure. This in turn reduces the cooling needed for these interior spaces, improving the economic and ecological performance of the architectural structure using the multilayer composite film 100.
• the IR radiation rejection layer 116 has a thickness, indicated by ⁇ in FIG.
• 1 A that can be within any of the following ranges: from 1 nm to 100 nm; from 10 nm to 50 nm; from 50 nm to 100 nm; from 25 nm to 75 nm; from 25 nm to 50 nm; and from 50 nm to 75 nm.
• the example of the IR radiation rejection layer 116 shown in FIG. 1 A is that of a metal film (alternatively referred to as a metal layer) deposited onto a surface of the structural polymer layer 108.
• the metal layer of the IR radiation rejection layer 116 may also include multiple layers of metal.
• the IR radiation rejection layer 116 on the structural polymer layer 108 can be adhered to the second major surface of the outer ETFE layer 104 via the fluoropolymer adhesive 112.
• Metal films can be continuous or be fabricated to include a pattern of metal portions and non-metal portions (often referred to as a "frit pattern").
• metals used to form a metal film for the IR radiation rejection layer 116 include, but are not limited to, aluminum, silver, copper, gold, metal oxides, combinations thereof, or other suitable metals or intermetallic compounds having an electronic structure that reflects at least 40% of incident IR radiation present in solar radiation. Sputtered metallic films can exhibit surface energies that facilitate adhesion to an opposed layer.
• the IR radiation rejection layer 116 can be adhered to the outer ETFE layer 104 directly.
• fluoropolymer adhesive layer 112 and IR radiation rejection layer 116 may be transposed from the figure so that the IR rejection layer is adjacent layer 104 and the adhesive layer is adjacent layer 108.
• multilayer composite film 120 shown in FIG. IB the separate fluoropolymer adhesive layer 112 and IR radiation rejection layer 116 are substituted for a single fluoropolymer adhesive layer 124 that also includes particles 128 that absorb and/or block IR radiation.
• This layer has a thickness ⁇ ' that can be in any of the ranges already introduced above as thickness ⁇ , thickness ⁇ , or combinations thereof.
• IR blocking materials include Sicopal® Black K 0095 from BASF and nanoparticles (e.g., titanium dioxide nanoparticles, silver nanoparticles, aluminum nanoparticles, and mixtures thereof).
• the particles 128 include those that alternate between reflecting IR radiation at high atmospheric temperatures (e.g., above 60°F) and transmitting IR radiation at low atmospheric temperatures (e.g., below 50°F).
• IR radiation rejection layer 116 and the fluoropolymer adhesive/IR layer 124 may include IR reflective dyes, IR absorbent dyes, UV absorbent dyes, light stabilizers, antioxidants, flame retardants, and mixtures thereof, in examples. Flame retardants may be added to any of the embodiments described herein to provide a flame resistance rating of V0 as measured according to the Underwriters Laboratories (UL) standard UL94, edition number 6, dated March 28, 2013.
• UL Underwriters Laboratories
• Embodiments described herein may also meet other fire related standards such as National Fire Protection Association (NFPA) standard 701, 2015 edition, and ASTM standard E84-16 for "Surface Burning Characteristics of Building Materials.”
• NFPA National Fire Protection Association
• embodiments such as the multilayer composite film 100 (described above), multilayer composite film (200), as well as various combinations that include multiple layers of any one or more of the individual layers 104, 108, 112, 116, 124, and 204 may be configured to comply with one or more of UL standard UL94, edition number 6, dated March 28, 2013, National Fire Protection Association (NFPA) standard 701, 2015 edition, and ASTM standard E84-16 for "Surface Burning Characteristics of Building Materials.”
• NFPA National Fire Protection Association
• the multilayer composite film 100 can still retain most of or all of the optical light transmissivity described above and is not only translucent but also transparent.
• FIG. 2 illustrates an ETFE multilayer composite film 200 that includes the multilayer composite film 100 and a second ETFE layer 204 attached to a surface of the structural polymer layer 108 opposite that of the outer ETFE layer 104.
• the second ETFE layer 204 configured to be disposed on as a surface on an interior of an architectural structure opposite the exterior surface, has a thickness, indicated in FIG. 2 by ⁇ , within any of the following ranges: 25 microns ( ⁇ ) to 250 ⁇ ; 25 ⁇ to 100 ⁇ ; 25 ⁇ to 75 ⁇ ; 25 ⁇ to 50 ⁇ ; 50 ⁇ to 150 ⁇ ; 50 ⁇ to 100 ⁇ ; 75 ⁇ to 200 ⁇ ; 75 ⁇ to 100 ⁇ ; 100 ⁇ to 200 ⁇ .
• a second fluoropolymer adhesive layer 114 that can have the same dimensions and composition as the fluoropolymer adhesive layer 112 and/or a fluoropolymer adhesive/IR layer 124 (shown only in FIG. IB) may be disposed between the second ETFE layer 204 and the structural polymer layer 108.
• IR reflectors or absorbents and other particles or dyes can be disposed in or adjacent to any of the adhesive layers 112, 114 that are used to join opposed polymer films.
• Example composite films were prepared according to the following procedure.
• a solution of fluoropolymer-based adhesive was prepared according to the formulation described above in Table 1.
• the prepared fluoropolymer-based adhesive solution was applied to a 125 Dm thick PET (V0 fire rating per UL94) film, which functioned as the structural polymer layer described above, at a coating weight of 15 g/m 2 .
• a first 25 ⁇ thick ETFE film was laminated onto the fluoropolymer-based adhesive bearing PET film.
• the fluoropolymer-based adhesive was then applied on the opposite side of the PET film at a coating weight of 15 g/m 2 and then laminated with a second 25 ⁇ thick ETFE film.
• the prepared experimental examples were subjected to uniaxial testing using an INSTRON 3360 dual column testing system.
• the experimental examples were strained at a uniform strain rate of 50 millimeters/minute.
• the stress-strain curve of the experimental example appears in FIG. 3 along with a comparison to a 250 ⁇ thick sheet of ETFE control sample that was strained separately but used the same uniaxial testing machine and strain rate identified above.
• the experimental example exhibits significantly higher Young's modulus than the ETFE alone.
• the experimental example also exhibits a single yield point at about 5% strain (at a stress of about 70 MPa) and had an ultimate yield stress of approximately 146 MPa (within normal measurement tolerances and natural variation within a population of samples).
• the experimental example was also subjected to 96 hours of highly accelerated stress testing (HAST) to test the adhesion between the layers.
• HAST highly accelerated stress testing
• the HAST testing was performed at 121 °C, 100% Relative Humidity (RH) and 1 atm.
• RH Relative Humidity
• the experimental example was also tested using the Damp Heat Test (International Electrochemical Commission standard number
• FIG. 4 illustrates a graph of reflectance data exhibited by an experimental example of a multilayer composite film of the present disclosure fabricated from two layers of ETFE film between which was adhered a layer of VikuitiTM film.
• the experimental sample was exposed to incident light having a plurality of wavelengths approximating a solar light wavelength distribution.
• IR reflectance data was collected using a PERKTN ELMER 950 spectrophotomer. These results are shown in FIG. 4. As is shown, IR reflectance is approximately 100% for IR wavelengths from approximately 780 nm to approximately 1000 nm. At the same time, reflectance in the visible range was less than 20%.
• FIGS. 5A-5C illustrate various joints that can be used for joining multilayer composite films together, in embodiments.
• the joints enable individual sheets of multilayer composite films of the present disclosure to be joined together into a larger architectural panel.
• individual sheets can be joined together to produce an architectural panel that is, for example, anywhere from lxl m to 25x25 m square before requiring external support (such as from a network of support cables).
• FIG. 5 A illustrates a lap joint in which individual sheets of the multilayer composite film 200 are overlapped by a distance designated in FIG. 5A as a seal width.
• the individual sheets can be joined using, for example, a heat seal that welds the sheets together, or an adhesive tape (e.g., a polyester base or a polyamide base thermoplastic heat activated adhesive tape) or an adhesive (e.g., a heat activated adhesive) disposed between the overlapping portions of the individual sheets of the multilayer composite film 200.
• a heat seal that welds the sheets together
• an adhesive tape e.g., a polyester base or a polyamide base thermoplastic heat activated adhesive tape
• an adhesive e.g., a heat activated adhesive
• FIG. 5B illustrates a butt joint in which proximate perimeter edges of two sheets of multilayer composite films 200 are butted together end-to-end and joined at the seal indicated using, for example, any of the techniques described above in the context of FIG. 5 A.
• FIG. 5C illustrates a variation of the butt joint shown in FIG. 5B.
• a strip 504 of single layer film or multilayer composite film 200 (or ETFE or other compatible polymer used as an outer layer 104) is joined to one or optionally both of the major surfaces of the sheets of multilayer composite films 200 joined via a butt joint so as to cover and extend beyond the butt joint.
• the multilayer composite films 100, 118, and 120 may be substituted for any of the films and/or strips shown in FIGS. 5A, 5B, and 5C.
• An adhesive for example a fluoropolymer adhesive such as a perfluoroalkyl vinyl ether, may be used in one or more of the seals between the polymer composite films or between the polymer composite film and one or more of strip 504.
• the tensile strength of these joints may be equal to, or better than, the tensile strength of the composite film itself.
• a seal width can be in any of the following ranges: from 0.5 cm to 10 cm; from 0.5 cm to 5 cm; from 0.5 cm to 2.5 cm; from 1 cm to 10 cm; from 1 cm to 5 cm; from 2 cm to 7 cm, greater than 1.0 cm, or less than 10 cm.
• FIG. 6 illustrates another embodiment of a multilayer composite film 200 configured to form a "cord edge" 500 that defines a volume and is formed by curling the multilayer composite film 200 around a rigid cord (such as EPDM rubber) that is then slid into a channel of a retaining structure.
• a rigid cord such as EPDM rubber
• the structure may be erected before or after the cord edge is inserted into the channel.
• the retaining structure can be attached or anchored (directly or indirectly) to the structure of the building or architectural application in which the multilayer composite film 200 is used as an element.
• the second major surface is adhered to itself to form the cord edge 500.
• the cord edge 500 may be inserted into the structural channel prior to sealing the composite.
• a first major surface may be fabricated from a different material than the second major surface because the first and second major surfaces need not be adhered together.
• the second major surface can be a fluoropolymer such as perfluoroalkyl vinyl ether and first major surface can be a non-fluorinated polymer including
• the second major surface may be the side of the composite that is exposed to the environment.
• the composite film can be adhered to itself using an adhesive, an adhesive tape or by welding, such as polymer welding, heat welding or ultrasonic welding.
• Adhesives can include, for example, fluorinated polymers such as perfluoroalkyl vinyl ether.
• FIG. 7A illustrates an example of the multilayer composite film 200 configured for use as an architectural element.
• one perimeter edge of the multilayer composite film 200 has been curled so that the second major surface of the second ETFE layer 204 contacts the first major surface of the outer ETFE layer 104.
• the two ETFE layers 204 may then be joined (e.g., using an adhesive, adhesive tape, or by heat sealing) around a cord to form the cord edge 500 as described above.
• the composite film can be rolled onto itself to form a cord edge in which the space typically occupied by a cord is filled by spiraled composite film material.
• FIG. 7B illustrates an alternative configuration for attaching a sheet or panel of the multilayer composite film 200 to a support cable.
• a strip 704 of either ETFE or of the multilayer composite film 200 is sealed to the sheet and/or panel of multiple sheets of the multilayer composite film 200 around a support cable 708.
• the seal widths indicated in FIG. 7B can be on the order of those described above. The same or similar sealing and adhesion techniques can be used.
• multilayer composite films 100, 118, and 120 may be substituted for any of the films and/or strips shown in FIGS. 6, 7A, and 7B.

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• Engineering & Computer Science (AREA)
• Architecture (AREA)
• Civil Engineering (AREA)
• Structural Engineering (AREA)
• Physics & Mathematics (AREA)
• Electromagnetism (AREA)
• Mechanical Engineering (AREA)
• Life Sciences & Earth Sciences (AREA)
• Wood Science & Technology (AREA)
• Laminated Bodies (AREA)
• Panels For Use In Building Construction (AREA)

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• 2016
  • 2016-10-28 US US15/337,971 patent/US11148405B2/en active Active
  • 2016-10-28 WO PCT/US2016/059533 patent/WO2017075499A1/en not_active Ceased
  • 2016-10-28 JP JP2018542997A patent/JP2018535862A/ja active Pending
  • 2016-10-28 US US15/772,236 patent/US20180311943A1/en not_active Abandoned
  • 2016-10-28 EP EP16860976.6A patent/EP3368305A4/en not_active Withdrawn
  • 2016-10-28 CA CA3002663A patent/CA3002663A1/en not_active Abandoned
• 2019
  • 2019-12-04 US US16/703,610 patent/US11345130B2/en active Active
• 2022
  • 2022-04-29 US US17/661,489 patent/US12226984B2/en active Active

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